WorldWideScience

Sample records for wo3 nanoparticle-modified immunoassay

  1. Enhanced photoelectrochemical and photocatalytic activity of WO3-surface modified TiO2 thin film

    Science.gov (United States)

    Qamar, Mohammad; Drmosh, Qasem; Ahmed, Muhammad I.; Qamaruddin, Muhammad; Yamani, Zain H.

    2015-02-01

    Development of nanostructured photocatalysts for harnessing solar energy in energy-efficient and environmentally benign way remains an important area of research. Pure and WO3-surface modified thin films of TiO2 were prepared by magnetron sputtering on indium tin oxide glass, and photoelectrochemical and photocatalytic activities of these films were studied. TiO2 particles were <50 nm, while deposited WO3 particles were <20 nm in size. An enhancement in the photocurrent was observed when the TiO2 surface was modified WO3 nanoparticles. Effect of potential, WO3 amount, and radiations of different wavelengths on the photoelectrochemical activity of TiO2 electrodes was investigated. Photocatalytic activity of TiO2 and WO3-modified TiO2 for the decolorization of methyl orange was tested.

  2. Electrochemical Behavior of TiO2 Nanoparticle Doped WO3 Thin Films

    Directory of Open Access Journals (Sweden)

    Suvarna R. Bathe

    2014-01-01

    Full Text Available Nanoparticle TiO2 doped WO3 thin films by pulsed spray pyrolysis technique have been studied on fluorine tin doped (FTO and glass substrate. XRD shows amorphous nature for undoped and anatase phase of TiO2 having (101 plane for nanoparticle TiO2 doped WO3 thin film. SEM shows microfibrous reticulated porous network for WO3 with 600 nm fiber diameter and nanocrystalline having size 40 nm for TiO2 nanoparticle doped WO3 thin film. TiO2 nanoparticle doped WO3 thin film shows ~95% reversibility due to may be attributed to nanocrystalline nature of the film, which helpful for charge insertion and deinsertion process. The diffusion coefficient for TiO2 nanoparticle doped WO3 film is less than undoped WO3.

  3. Anti-tumor activity of self-charged (Eu,Ca):WO3 and Eu:CaWO4 nanoparticles

    International Nuclear Information System (INIS)

    Lin, Cao; Cong, Wang; De'An, Pan; Jiexin, Cao; Ping, Che; Volinsky, Alex A.

    2012-01-01

    Non-stoichiometric (Eu,Ca):WO 3 and Eu:CaWO 4 nanoparticles with anti-tumor activity are synthesized in a sol-gel method by adding excessive Eu 3+ and Ca 2+ ions to tungsten oxide crystal structure. Colorimetric assay shows that 10 nm (Eu,Ca):WO 3 and Eu:CaWO 4 nanoparticles can effectively inhibit growth of mammary cancer cells without any harm to normal cells. Nanoparticles are characterized by X-ray diffraction, high resolution transmission electron microscopy and fluorescence optical spectrometry. Nanomaterials, insoluble in synthesized water, have complicated self-charging surfaces that trap mammary cancer cells. Surface self-charging effect is suggested as the inhibition mechanism. (author)

  4. Photocatalytic properties of h-WO{sub 3} nanoparticles obtained by annealing and h-WO{sub 3} nanorods prepared by hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Boyadjiev, Stefan I., E-mail: boiajiev@gmail.com [MTA-BME Technical Analytical Chemistry Research Group, Szent Gellért tér 4, Budapest, H-1111 (Hungary); Nagy-Kovács, Teodóra [Budapest University of Technology and Economics, Department of Inorganic and Analytical Chemistry, Szent Gellért tér 4, Budapest, H-1111 (Hungary); Lukács, István [Hungarian Academy of Sciences, Research Centre for Energy, Institute of Technical Physics and Materials Science, H-1121 Budapest, Konkoly Thege M. út 29-33 (Hungary); Szilágyi, Imre M., E-mail: imre.szilagyi@mail.bme.hu [MTA-BME Technical Analytical Chemistry Research Group, Szent Gellért tér 4, Budapest, H-1111 (Hungary); Budapest University of Technology and Economics, Department of Inorganic and Analytical Chemistry, Szent Gellért tér 4, Budapest, H-1111 (Hungary)

    2016-03-25

    In the present study, two different methods for preparing hexagonal WO{sub 3} (h-WO{sub 3}) photocatalysts were used - controlled thermal decomposition and hydrothermal synthesis. WO{sub 3} nanoparticles with hexagonal structure were obtained by annealing (NH{sub 4}){sub x}WO{sub 3-y} at 500 °C in air. WO{sub 3} nanorods were prepared by a hydrothermal method using sodium tungstate Na{sub 2}WO{sub 4}, HCl, (COOH){sub 2} and NaSO{sub 4} precursors at 200 °C. The formation, morphology, structure and composition of the as-prepared nanoparticles and nanorods were studied by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and scanning electron microscopy combined with energy-dispersive X-ray spectroscopy (SEM-EDX). The photocatalytic activity of the h-WO{sub 3} nanoparticles and nanorods was studied by decomposing methyl orange in aqueous solution under UV light irradiation.

  5. Preparation and characterization of WO{sub 3} nanoparticles, WO{sub 3}/TiO{sub 2} core/shell nanocomposites and PEDOT:PSS/WO{sub 3} composite thin films for photocatalytic and electrochromic applications

    Energy Technology Data Exchange (ETDEWEB)

    Boyadjiev, Stefan I., E-mail: boiajiev@gmail.com [MTA-BME Technical Analytical Chemistry Research Group, Szent Gellért tér 4, Budapest, H-1111 (Hungary); Santos, Gustavo dos Lopes; Szűcs, Júlia [Budapest University of Technology and Economics, Department of Inorganic and Analytical Chemistry, Szent Gellért tér 4, Budapest, H-1111 (Hungary); Szilágyi, Imre M., E-mail: imre.szilagyi@mail.bme.hu [MTA-BME Technical Analytical Chemistry Research Group, Szent Gellért tér 4, Budapest, H-1111 (Hungary); Budapest University of Technology and Economics, Department of Inorganic and Analytical Chemistry, Szent Gellért tér 4, Budapest, H-1111 (Hungary)

    2016-03-25

    In this study, monoclinic WO{sub 3} nanoparticles were obtained by thermal decomposition of (NH{sub 4}){sub x}WO{sub 3} in air at 600 °C. On them by atomic layer deposition (ALD) TiO{sub 2} films were deposited, and thus core/shell WO{sub 3}/TiO{sub 2} nanocomposites were prepared. We prepared composites of WO{sub 3} nanoparticles with conductive polymer as PEDOT:PSS, and deposited thin films of them on glass and ITO substrates by spin coating. The formation, morphology, composition and structure of the as-prepared pure and composite nanoparticles, as well thin films, were studied by TEM, SEM-EDX and XRD. The photocatalytic activity of both the WO{sub 3} and core/shell WO{sub 3}/TiO{sub 2} nanoparticles was studied by decomposing methyl orange in aqueous solution under UV light irradiation. Cyclic voltammetry measurements were performed on the composite PEDOT:PSS/WO{sub 3} thin films, and the coloring and bleaching states were studied.

  6. Fungus mediated biosynthesis of WO3 nanoparticles using Fusarium solani extract

    Science.gov (United States)

    Kavitha, N. S.; Venkatesh, K. S.; Palani, N. S.; Ilangovan, R.

    2017-05-01

    Currently nanoparticles were synthesized by emphasis bioremediation process due to less hazardous, eco-friendly and imperative applications on biogenic process. Fungus mediated biosynthesis strategy has been developed to prepare tungsten oxide nanoflakes (WO3, NFs) using the plant pathogenic fungus F.solani. The powder XRD pattern revealed the monoclinic crystal structure with improved crystalline nature of the synthesized WO3 nanoparticles. FESEM images showed the flake-like morphology of WO3, with average thickness and length around 40 nm and 300 nm respectively. The Raman spectrum of WO3 NFs showed their characteristic vibration modes that revealed the defect free nature of the WO3 NFs. Further, the elemental analysis indicated the stoichiometric composition of WO3 phase.

  7. WO3 nanorods-modified carbon electrode for sustained electron uptake from Shewanella oneidensis MR-1 with suppressed biofilm formation

    International Nuclear Information System (INIS)

    Zhang, Feng; Yuan, Shi-Jie; Li, Wen-Wei; Chen, Jie-Jie; Ko, Chi-Chiu; Yu, Han-Qing

    2015-01-01

    Highlights: • WO 3 nanorods-modified carbon paper was used as the anode of MFC. • WO 3 nanorods suppressed biofilm growth on the electrode surface. • Sustained electron transfer from cells to electrode via riboflavin was achieved. • C–WO 3 nanorods enable stable and efficient EET process in long-time operation. - Abstract: Carbon materials are widely used as electrodes for bioelectrochemical systems (BES). However, a thick biofilm tends to grow on the electrode surface during continuous operation, resulting in constrained transport of electrons and nutrients at the cell-electrode interface. In this work, we tackled this problem by adopting a WO 3 -nanorods modified carbon electrode (C–WO 3 nanorods), which completely suppressed the biofilm growth of Shewanella Oneidensis MR-1. Moreover, the C–WO 3 nanorods exhibited high electric conductivity and strong response to riboflavin. These two factors together make it possible for the C–WO 3 nanorods to maintain a sustained, efficient process of electron transfer from the MR-1 planktonic cells. As a consequence, the microbial fuel cells with C–WO 3 nanorods anode showed more stable performance than the pure carbon paper and WO 3 -nanoparticles systems in prolonged operation. This work suggests that WO 3 nanorods have the potential to be used as a robust and biofouling-resistant electrode material for practical bioelectrochemical applications

  8. Synthesis and photoluminescence properties of Sm3+-doped CaWO4 nanoparticles

    International Nuclear Information System (INIS)

    Xiao Qi; Zhou Qitao; Li Ming

    2010-01-01

    The Sm 3+ -doped CaWO 4 nanoparticles were synthesized by hydrothermal method. The room temperature photoluminescence (PL) spectra of Sm 3+ -doped CaWO 4 nanoparticles doped with different Sm 3+ concentrations under 405 nm excitation have been investigated. The PL spectra showed four strong emission peaks at 460, 571, 609, and 653 nm. The first emission peak at 460 nm could be due to a structural defect of the lattice, an oxygen-deficient WO 3 complex. The other three emissions at 571, 609, and 653 nm were due to the f-f forbidden transitions of the 4f electrons of Sm 3+ , corresponding to 4 G 5/2 → 6 H 5/2 (571 nm), 6 H 7/2 (609 nm), and 6 H 9/2 (653 nm), respectively. In addition, the optimum Sm 3+ concentration in CaWO 4 nanoparticles for optical emission was determined to be 1.0%. The Sm 3+4 G 5/2 → 6 H 7/2 (609 nm) emission intensity of Sm 3+ -doped CaWO 4 nanoparticles significantly increased with the increase of Sm 3+ concentration, and showed a maximum when Sm 3+ doping content was 1.0%. If Sm 3+ concentration continued to increase, namely more than 1.0%, the Sm 3+4 G 5/2 → 6 H 7/2 emission intensity would decrease. The present materials might be a promising phosphor for white-light LED applications.

  9. Chemiluminescence enzyme immunoassay based on magnetic nanoparticles for detection of hepatocellular carcinoma marker glypican-3

    Directory of Open Access Journals (Sweden)

    Qian-Yun Zhang

    2011-08-01

    Full Text Available Glypican-3 (GPC3 is reported as a great promising tumor marker for hepatocellular carcinoma (HCC diagnosis. Highly sensitive and accurate analysis of serum GPC3 (sGPC3, in combination with or instead of traditional HCC marker alpha-fetoprotein (AFP, is essential for early diagnosis of HCC. Biomaterial-functionalized magnetic particles have been utilized as solid supports with good biological compatibility for sensitive immunoassay. Here, the magnetic nanoparticles (MnPs and magnetic microparticles (MmPs with carboxyl groups were further modified with streptavidin, and applied for the development of chemiluminescence enzyme immunoassay (CLEIA. After comparing between MnPs- and MmPs-based CLEIA, MnPs-based CLEIA was proved to be a better method with less assay time, greater sensitivity, better linearity and longer chemiluminescence platform. MnPs-based CLEIA was applied for detection of sGPC3 in normal liver, hepatocirrhosis, secondary liver cancer and HCC serum samples. The results indicated that sGPC3 was effective in diagnosis of HCC with high performance. Keywords: Magnetic nanoparticle, Magnetic microparticle, Chemiluminescence enzyme immunoassay, Glypican-3, Hepatocellular carcinoma

  10. Enhanced electrochromic coloration in Ag nanoparticle decorated WO3 thin films

    International Nuclear Information System (INIS)

    Kharade, Rohini R.; Mali, Sawanta S.; Patil, Satish P.; Patil, Kashinath R.; Gang, Myong G.; Patil, Pramod S.; Kim, Jin H.; Bhosale, Popatrao N.

    2013-01-01

    Highlights: • Electrochromic WO 3 /Ag nanocomposites prepared by hybrid physico-chemical route. • XRD and XPS results confirm formation of Ag 8 W 4 O 16 phase. • WO 3 /Ag thin films showed good optical transmittance change and coloration efficiency. • SPR enhanced coloration and bleaching mechanism is well explained for electrochromism. • Color stimuli are quantified using CIE chromaticity principles. -- Abstract: WO 3 /Ag composite thin films were prepared by microwave assisted sol–gel synthesis (MW-SGS) of WO 3 followed by vacuum evaporation of Ag nanoparticles and their enhanced electrochromic coloration was investigated. The composition and morphology of WO 3 thin films with different thickness of Ag layer obtained by vacuum evaporation were investigated. Distinct plasmon absorption bands of Ag nanoparticle thin films were obtained. The optical band gap energy of WO 3 /Ag films decreased with increasing the Ag layer thickness. The surface of these films has been examined using X-ray photoelectron spectroscopy (XPS) to gain information about the chemical states of species present at surfaces. Experimental results indicated that the conductivity of the films increased after surface modification by Ag layer. To investigate the origin of enhanced electrochromic absorption in optical properties, working electrode consisting of WO 3 /Ag thin film was used and observed the optical properties during electrochemical reaction. It was found that composite electrode shows enhancement in electrochromic properties in terms of optical modulation (ΔOD) and coloration efficiency (η)

  11. Cr2O3 nanoparticle-functionalized WO3 nanorods for ethanol gas sensors

    Science.gov (United States)

    Choi, Seungbok; Bonyani, Maryam; Sun, Gun-Joo; Lee, Jae Kyung; Hyun, Soong Keun; Lee, Chongmu

    2018-02-01

    Pristine WO3 nanorods and Cr2O3-functionalized WO3 nanorods were synthesized by the thermal evaporation of WO3 powder in an oxidizing atmosphere, followed by spin-coating of the nanowires with Cr2O3 nanoparticles and thermal annealing in an oxidizing atmosphere. Scanning electron microscopy was used to examine the morphological features and X-ray diffraction was used to study the crystallinity and phase formation of the synthesized nanorods. Gas sensing tests were performed at different temperatures in the presence of test gases (ethanol, acetone, CO, benzene and toluene). The Cr2O3-functionalized WO3 nanorods sensor showed a stronger response to these gases relative to the pristine WO3 nanorod sensor. In particular, the response of the Cr2O3-functionalized WO3 nanorods sensor to 200 ppm ethanol gas was 5.58, which is approximately 4.4 times higher that of the pristine WO3 nanorods sensor. Furthermore, the Cr2O3-functionalized WO3 nanorods sensor had a shorter response and recovery time. The pristine WO3 nanorods had no selectivity toward ethanol gas, whereas the Cr2O3-functionalized WO3 nanorods sensor showed good selectivity toward ethanol. The gas sensing mechanism of the Cr2O3-functionalized WO3 nanorods sensor toward ethanol is discussed in detail.

  12. Preparation and characterization of zinc and copper co-doped WO3 nanoparticles: Application in photocatalysis and photobiology.

    Science.gov (United States)

    Mohammadi, Sanaz; Sohrabi, Maryam; Golikand, Ahmad Nozad; Fakhri, Ali

    2016-08-01

    In this study, pure, Zn, Cu, Zn,Cu co-doped WO3 nanoparticles samples were prepared by precipitation and co-precipitation methods. These nanoparticles were characterized by field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), energy dispersive X-ray spectrometer (EDX), Dynamic light scattering (DLS), UV-visible and photoluminescence (PL) spectroscopy. The synthesized pure, Zn, Cu, Zn,Cu co-doped WO3 nanoparticles have smart optical properties and average sizes with 3.2, 3.12, 3.08 and 2.97eV of band-gap, 18.1, 23.2, 25.7 and 30.2nm, respectively. Photocatalytic activity of four nanoparticles was studying towards degradation of gentamicin antibiotic under ultraviolet and visible light irradiation. The result showed that Zn,Cu co-doped WO3 possessed high photocatalytic activity. The photocatalytic activity of WO3 nanoparticles could be remarkably increased by doping the Zn and Cu impurity. This can be attributed to the fact that the red shift of absorption edge and the trapping effect of the mono and co-doped WO3 nanoparticles. The research result presents a general and effective way to prepare different photocatalysts with enhanced visible and UV light-driven photocatalytic performance. Antibacterial activity of four different WO3 nanoparticles against Escherichia coli bacterium has been assessed by the agar disc method under light irradiation and dark medium. It is concluded from the present findings that WO3 nanoparticles can be used as an efficient antibacterial agent. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Synthesis, characterization and liquefied petroleum gas (LPG) sensing properties of WO3 nano-particles

    Science.gov (United States)

    Singh, Subhash; Majumder, S. B.

    2018-05-01

    Metal oxide sensors, such as ZnO, SnO2, and WO3 etc. have been utilized for several decades for low-costd etection of combustible and toxic gases. In the present work tungsten oxide (WO3) nanoparticles have been prepared by using an economic wet chemical synthesis route. To understand the phase formation behavior of the synthesized powders, X-ray diffraction analysis has been performed. The microstructure evolution of the synthesized powders was characterized by field-emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM). The calcined phase pure WO3 nanoparticles are investigated in terms of LPG gas sensing properties. The gas sensing measurements has been done in two different mode of operation (namely static and dynamic measurements). The degree of oxygen deficiency in the WO3 sensor also affected the sensor properties and the optimum oxygen content of WO3 was necessary to get high sensitivity for LPG. The WO3 sensor shows the excellent sensor properties for LPG at the operating temperature of 250°C.

  14. N, Fe and WO3 modified TiO2 for degradation of formaldehyde

    International Nuclear Information System (INIS)

    Tong Haixia; Zhao Li; Li Dan; Zhang Xiongfei

    2011-01-01

    Graphical abstract: The undoped TiO 2 powder (T(0)) shows strong photoabsorption only at wavelengths shorter than 400 nm, and while Fe 3+ and N-doped TiO 2 nanoparticles show photoabsorption in visible region and the absorption edge shifts to a longer wavelength. WO 3 compounding also benefits the photoabsorption in visible region. Display Omitted Highlights: → The preparation of the catalysts co-doped by Fe, N and compounded by WO 3 . → The obvious sculptured 'pattern' of the catalysts doped by Fe in the SEM images. → Strengthened photoabsorption to visible light of the modified catalysts from UV-DRS analysis. - Abstract: Butyltitanate, ethanol and glacial acetic acid were chosen as titanium source, solvent and chelating agent, respectively, via a sol-gel method combined impregnation method to prepare N, Fe co-doped and WO 3 compounded photocatalyst TiO 2 powder. The synthesized products were characterized by X-ray diffraction (XRD), diffuse reflectance UV-Vis spectra (UV-DRS), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Photocatalytic degradation of formaldehyde was employed to investigate the catalytic activity. The results show that the degradation rate is 77.61% in 180 min under UV light irradiation when the concentration of N is fixed on, and the optimum proportioning ratio of n(Fe):n(W):n(Ti) is 0.5:2:100.

  15. Dissimilar mechanism of executing hole transfer by WO{sub 3} and MoO{sub 3} nanoparticles in organic solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Park, Eung-Kyu; Kim, Jae-Hyoung; Kim, Ji-Hwan; Park, Min-Ho; Lee, Dong-Hoon; Kim, Yong-Sang, E-mail: yongsang@skku.edu

    2015-07-31

    We investigated the effect of metal oxide nanoparticles (NPs) in poly (3,4 ethylenedioxythiophence):poly (styrene-sulfonate) layer for the light harvestation in poly (3-hexylthiophene):[6,6]-pheny-C{sub 61}-butyric acid methyl ester organic solar cells. The role of tungsten trioxide nanoparticles (WO{sub 3}) and molybdenum trioxide nanoparticles (MoO{sub 3}) in enhancing the efficiency of solar cells was compared. Due to the difference in the energy band structure of the two nanoparticles, the WO{sub 3} NPs acted as a hole blocking layer, whereas MoO{sub 3} NPs helped in the hole transfer. The solar cell with WO{sub 3} NPs at 1.5 wt% concentration showed a power conversion efficiency of 4.22% under AM 1.5G illumination and the device blended with 2 wt% of MoO{sub 3} NPs showed a power conversion efficiency of 4.40%. We measured various electrical properties including, electrochemical impedance spectroscopy and recombination mechanisms using the light intensity dependent current–voltage measurement of organic solar cell. - Highlights: • An organic solar cell was fabricated with WO{sub 3} or MoO{sub 3} NPs mixed PEDOT:PSS layer. • The effects of metallic NPs in PEDOT:PSS light harvesting system was investigated. • WO{sub 3} NPs acted as a hole blocking layer and MoO{sub 3} NPs helped in hole transporting. • The MoO{sub 3} NPs gave higher performance, reduced charge recombination and low resistance.

  16. Immobilized WO3 nanoparticles on graphene oxide as a photo-induced antibacterial agent against UV-resistant Bacillus pumilus

    Science.gov (United States)

    Hosseini, Farshad; Rasuli, Reza; Jafarian, Vahab

    2018-04-01

    We present the antibacterial and photo-catalytic activity of immobilized WO3 nanoparticles on graphene oxide sheets. WO3 nanoparticles were immobilized on graphene oxide using the arc discharge method in arc currents of 5, 20, 40 and 60 A. Tauc plots of the UV-visible spectra show that the band gap of the prepared samples decreases (to ~2.7 eV) with respect to the WO3 nanoparticles. Photo-catalytic activity was examined by the degradation of rhodamine B under ultra-violet irradiation and the results show that the photo-catalytic activity of WO3 nanoparticles is increased by immobilizing them on graphene oxide sheets. In addition, the photo-degradation yield of the samples prepared by the 5 A arc current is 84% in 120 min, which is more than that of the other samples. The antibacterial activity of the prepared samples was studied against Bacillus pumilus (B. pumilus) bacteria, showing high resistance to ultra-violet exposure. Our results show that the bare and immobilized WO3 nanoparticles become more active under UV irradiation and their antibacterial properties are comparable with Ag nanoparticles. Besides this, the results show that although the photo-catalytic activity of the post-annealed samples at 500 °C is less than the as-prepared samples, it is, however, more active against B. pumilus bacteria under UV irradiation.

  17. Synthesis of WO3 nanoparticles by citric acid-assisted precipitation and evaluation of their photocatalytic properties

    International Nuclear Information System (INIS)

    Sánchez-Martínez, D.; Martínez-de la Cruz, A.; López-Cuéllar, E.

    2013-01-01

    Graphical abstract: Display Omitted Highlights: ► WO 3 nanoparticles were synthesized by a simple citric acid-assisted precipitation. ► WO 3 photocatalyst was able to the partial mineralization of rhB, IC and MO. ► WO 3 can be considered as a photocatalyst active under visible light irradiation. -- Abstract: WO 3 nanoparticles were synthesized by citric acid-assisted precipitation method using a 1:1.5 molar ratio of ammonium paratungstate hydrate (H 42 N 10 O 42 W 12 ·xH 2 O):citric acid (C 6 H 8 O 7 ). The formation of monoclinic crystal structure of WO 3 at different temperatures was confirmed by X-ray powder diffraction (XRD). The characterization of the samples synthesized was complemented by transmission electron microscopy (TEM), Brunauer–Emmitt–Teller surface area (BET) and diffuse reflectance spectroscopy (DRS). According to the thermal treatment followed during the synthesis of WO 3 , the morphology of the nanoparticles formed was characterized by rectangular and ovoid shapes. The photocatalytic activity of WO 3 obtained under different experimental conditions was evaluated in the degradation of rhodamine B (rhB), indigo carmine (IC), methyl orange (MO), and Congo red (CR) in aqueous solution under UV and UV–vis radiation. The highest photocatalytic activity was observed in the sample obtained by thermal treatment at 700 °C. In general, the sequence of degradation of the organic dyes was: indigo carmine (IC) > rhodamine B (rhB) > methyl orange (MO) > Congo red (CR). The mineralization degree of organic dyes by WO 3 photocatalysts was determined by total organic carbon analysis (TOC) reaching percentages of mineralization of 82% (rhB), 85% (IC), 28% (MO), and 7% (CR) for 96 h of lamp irradiation.

  18. WO3/Pt nanoparticles are NADPH oxidase biomimetics that mimic effector cells in vitro and in vivo

    International Nuclear Information System (INIS)

    Clark, Andrea J; Coury, Emma L; Meilhac, Alexandra M; Petty, Howard R

    2016-01-01

    To provide a means of delivering an artificial immune effector cell-like attack on tumor cells, we report the tumoricidal ability of inorganic WO 3 /Pt nanoparticles that mimic a leukocyte’s functional abilities. These nanoparticles route electrons from organic structures and electron carriers to form hydroxyl radicals within tumor cells. During visible light exposure, WO 3 /Pt nanoparticles manufacture hydroxyl radicals, degrade organic compounds, use NADPH, trigger lipid peroxidation, promote lysosomal membrane disruption, promote the loss of reduced glutathione, and activate apoptosis. In a model of advanced breast cancer metastasis to the eye’s anterior chamber, we show that WO 3 /Pt nanoparticles prolong the survival of 4T1 tumor-bearing Balb/c mice. This new generation of inorganic photosensitizers do not photobleach, and therefore should provide an important therapeutic advance in photodynamic therapy. As biomimetic nanoparticles destroy targeted cells, they may be useful in treating ocular and other forms of cancer. (paper)

  19. WO3/Pt nanoparticles are NADPH oxidase biomimetics that mimic effector cells in vitro and in vivo

    Science.gov (United States)

    Clark, Andrea J.; Coury, Emma L.; Meilhac, Alexandra M.; Petty, Howard R.

    2016-02-01

    To provide a means of delivering an artificial immune effector cell-like attack on tumor cells, we report the tumoricidal ability of inorganic WO3/Pt nanoparticles that mimic a leukocyte’s functional abilities. These nanoparticles route electrons from organic structures and electron carriers to form hydroxyl radicals within tumor cells. During visible light exposure, WO3/Pt nanoparticles manufacture hydroxyl radicals, degrade organic compounds, use NADPH, trigger lipid peroxidation, promote lysosomal membrane disruption, promote the loss of reduced glutathione, and activate apoptosis. In a model of advanced breast cancer metastasis to the eye’s anterior chamber, we show that WO3/Pt nanoparticles prolong the survival of 4T1 tumor-bearing Balb/c mice. This new generation of inorganic photosensitizers do not photobleach, and therefore should provide an important therapeutic advance in photodynamic therapy. As biomimetic nanoparticles destroy targeted cells, they may be useful in treating ocular and other forms of cancer.

  20. Electrodeposition of WO3 nanoparticles into surface mounted metal-organic framework HKUST-1 thin films

    Science.gov (United States)

    Yoo, Hyeonseok; Welle, Alexander; Guo, Wei; Choi, Jinsub; Redel, Engelbert

    2017-03-01

    We describe a novel procedure to fabricate WO3@surface-mounted metal-organic framework (SURMOF) hybrid materials by electrodeposition of WO3 nanoparticles into HKUST-1, also termed Cu3(BTC)2 SURMOFs. These materials have been characterized using x-ray diffraction, time-of-flight secondary ion mass spectrometry, scanning electron microscopy, x-ray photoelectron spectroscopy as well as linear sweep voltammetry. The WO3 semiconductor/SURMOF heterostructures were further tested as hybrid electrodes in their performance for hydrogen evolution reaction from water.

  1. Synthesis of WO{sub 3} nanoparticles by citric acid-assisted precipitation and evaluation of their photocatalytic properties

    Energy Technology Data Exchange (ETDEWEB)

    Sánchez-Martínez, D. [Departamento de Ecomateriales y Energía, Facultad de Ingeniería Civil (UANL), Ciudad Universitaria, C.P. 66451, San Nicolás de los Garza, N.L. (Mexico); Martínez-de la Cruz, A., E-mail: azael70@yahoo.com.mx [Facultad de Ingeniería Mecánica y Eléctrica, Universidad Autónoma de Nuevo León, Ciudad Universitaria, C.P. 66451, San Nicolás de los Garza, N.L. (Mexico); López-Cuéllar, E. [Facultad de Ingeniería Mecánica y Eléctrica, Universidad Autónoma de Nuevo León, Ciudad Universitaria, C.P. 66451, San Nicolás de los Garza, N.L. (Mexico)

    2013-02-15

    Graphical abstract: Display Omitted Highlights: ► WO{sub 3} nanoparticles were synthesized by a simple citric acid-assisted precipitation. ► WO{sub 3} photocatalyst was able to the partial mineralization of rhB, IC and MO. ► WO{sub 3} can be considered as a photocatalyst active under visible light irradiation. -- Abstract: WO{sub 3} nanoparticles were synthesized by citric acid-assisted precipitation method using a 1:1.5 molar ratio of ammonium paratungstate hydrate (H{sub 42}N{sub 10}O{sub 42}W{sub 12}·xH{sub 2}O):citric acid (C{sub 6}H{sub 8}O{sub 7}). The formation of monoclinic crystal structure of WO{sub 3} at different temperatures was confirmed by X-ray powder diffraction (XRD). The characterization of the samples synthesized was complemented by transmission electron microscopy (TEM), Brunauer–Emmitt–Teller surface area (BET) and diffuse reflectance spectroscopy (DRS). According to the thermal treatment followed during the synthesis of WO{sub 3}, the morphology of the nanoparticles formed was characterized by rectangular and ovoid shapes. The photocatalytic activity of WO{sub 3} obtained under different experimental conditions was evaluated in the degradation of rhodamine B (rhB), indigo carmine (IC), methyl orange (MO), and Congo red (CR) in aqueous solution under UV and UV–vis radiation. The highest photocatalytic activity was observed in the sample obtained by thermal treatment at 700 °C. In general, the sequence of degradation of the organic dyes was: indigo carmine (IC) > rhodamine B (rhB) > methyl orange (MO) > Congo red (CR). The mineralization degree of organic dyes by WO{sub 3} photocatalysts was determined by total organic carbon analysis (TOC) reaching percentages of mineralization of 82% (rhB), 85% (IC), 28% (MO), and 7% (CR) for 96 h of lamp irradiation.

  2. Fabrication and characterization of WO3/Ag/WO3 multilayer transparent anode with solution-processed WO3 for polymer light-emitting diodes.

    Science.gov (United States)

    Jeon, Kangmin; Youn, Hongseok; Kim, Seongbeom; Shin, Seongbeom; Yang, Minyang

    2012-05-15

    The dielectric/metal/dielectric multilayer is suitable for a transparent electrode because of its high-optical and high-electrical properties; however, it is fabricated by an expensive and inefficient multistep vacuum process. We present a WO3/Ag/WO3 (WAW) multilayer transparent anode with solution-processed WO3 for polymer light-emitting diodes (PLEDs). This WAW multilayer not only has high transmittance and low resistance but also can be easily and rapidly fabricated. We devised a novel method to deposit a thin WO3 layer by a solution process in an air environment. A tungstic acid solution was prepared from an aqueous solution of Na2WO4 and then converted to WO3 nanoparticles (NPs) by a thermal treatment. Thin WO3 NP layers form WAW multilayer with a thermal-evaporated Ag layer, and they improve the transmittance of the WAW multilayer because of its high transmittance and refractive index. Moreover, the surface of the WO3 layer is homogeneous and flat with low roughness because of the WO3 NP generation from the tungstic acid solution without aggregation. We performed optical simulation and experiments, and the optimized WAW multilayer had a high transmittance of 85% with a sheet resistance of 4 Ω/sq. Finally, PLEDs based on the WAW multilayer anode achieved a maximum luminance of 35,550 cd/m2 at 8 V, and this result implies that the solution-processed WAW multilayer is appropriate for use as a transparent anode in PLEDs.

  3. Hydrogel nanoparticle based immunoassay

    Science.gov (United States)

    Liotta, Lance A; Luchini, Alessandra; Petricoin, Emanuel F; Espina, Virginia

    2015-04-21

    An immunoassay device incorporating porous polymeric capture nanoparticles within either the sample collection vessel or pre-impregnated into a porous substratum within fluid flow path of the analytical device is presented. This incorporation of capture particles within the immunoassay device improves sensitivity while removing the requirement for pre-processing of samples prior to loading the immunoassay device. A preferred embodiment is coreshell bait containing capture nanoparticles which perform three functions in one step, in solution: a) molecular size sieving, b) target analyte sequestration and concentration, and c) protection from degradation. The polymeric matrix of the capture particles may be made of co-polymeric materials having a structural monomer and an affinity monomer, the affinity monomer having properties that attract the analyte to the capture particle. This device is useful for point of care diagnostic assays for biomedical applications and as field deployable assays for environmental, pathogen and chemical or biological threat identification.

  4. First report on hemoglobin electrostatic immobilization on WO3 nanoparticles: application in the simultaneous determination of levodopa, uric acid, and folic acid.

    Science.gov (United States)

    Ghodsi, Javad; Rafati, Amir Abbas; Shoja, Yalda

    2016-05-01

    This work describes the first report about the simultaneous determination of levodopa (L-DOPA) with folic acid (FA) and uric acid (UA) based on electrocatalytic oxidation of L-DOPA with peroxidase properties of hemoglobin (Hb) in the presence of H2O2 as Hb activator. Bovine Hb was electrostatically immobilized on WO3 nanoparticles (WO3NPs) in pH between Hb and WO3NP isoelectric points, and subsequently, a carbon paste electrode (CPE) was modified with the obtained WO3NPs-Hb and multiwalled carbon nanotubes (MWCNTs). The resulting biosensor supplied a sensitive and suitably stable biosensor for the simultaneous determination of L-DOPA, UA, and FA. The obtained linear range and detection limit for L-DOPA, UA, and FA were completely acceptable, and the biosensor response time for these molecules was relatively short so that it reaches about 95 % of its maximum response in less than 10 s. The applicability of the current biosensor was confirmed with the determination of L-DOPA in the presence of fixed amounts of FA and UA in some real samples by the standard addition method.

  5. Characterization of Mixed xWO3(1-xY2O3 Nanoparticle Thick Film for Gas Sensing Application

    Directory of Open Access Journals (Sweden)

    M. H. Shahrokh Abadi

    2010-05-01

    Full Text Available Microstructural, topology, inner morphology, and gas-sensitivity of mixed xWO3(1-xY2O3 nanoparticles (x = 1, 0.95, 0.9, 0.85, 0.8 thick-film semiconductor gas sensors were studied. The surface topography and inner morphological properties of the mixed powder and sensing film were characterized with X-ray diffraction (XRD, atomic force microscopy (AFM, transmission electron microscopy (TEM, and scanning electron microscopy (SEM. Also, gas sensitivity properties of the printed films were evaluated in the presence of methane (CH4 and butane (C4H10 at up to 500 °C operating temperature of the sensor. The results show that the doping agent can modify some structural properties and gas sensitivity of the mixed powder.

  6. A facile synthesis of ZnWO{sub 4} nanoparticles by microwave assisted technique and its application in photocatalysis

    Energy Technology Data Exchange (ETDEWEB)

    Garadkar, K.M., E-mail: kmg_chem@unishivaji.ac.in [Nanomaterials Research Laboratory, Department of Chemistry, Shivaji University, Kolhapur 416 004, MS (India); Ghule, L.A. [Nanomaterials Research Laboratory, Department of Chemistry, Shivaji University, Kolhapur 416 004, MS (India); Sapnar, K.B.; Dhole, S.D. [Microtron Accelerator Laboratory, Department of Physics, University of Pune, Pune 411 007, MS (India)

    2013-03-15

    Highlights: ► Nanocrystalline ZnWO{sub 4} particles were successfully prepared by a microwave method. ► Spherical morphology with a 10 nm size. ► The band is 3.4 eV. ► The photodegradation of RhB was 95% within 25 min. - Abstract: A simple microwave assisted technique has been successfully developed to synthesize ZnWO{sub 4} nanoparticles. The X-ray diffraction results indicated that the synthesized nanoparticles exhibited only wolframite structure. Structural, morphological and optical properties of ZnWO{sub 4} nanoparticles have been analyzed by XRD, SEM, TEM EDAX, UV–vis and FT-IR spectral measurements. The transmission electron microscopy (TEM) image revealed that particle size of ZnWO{sub 4} nanoparticles was found to be 10 nm, the band-gap of ZnWO{sub 4} nanoparticles was found to be 3.4 eV. The photocatalytic activities for aqueous Rhodamine B and Methylene Blue samples were investigated and observed that ZnWO{sub 4} nanoparticles exhibited highly enhanced photocatalytic activity towards RhB than MB.

  7. Effect of annealing on the structural, optical and emissive properties of SrWO4:Ln3+ (Dy3+, Eu3+ and Sm3+) nanoparticles

    Science.gov (United States)

    Maheshwary; Singh, B. P.; Singh, R. A.

    2016-01-01

    Lanthanide ions, Ln3+ (Dy3+, Eu3+ and Sm3+) doped SrWO4 nanoparticles were synthesized using ethylene glycol (EG) as a capping agent as well as reaction medium. The X-ray diffraction (XRD) study reveals that all the Ln3+ (Dy3+, Eu3+ and Sm3+) doped samples are well crystalline in nature with a tetragonal scheelite structure of SrWO4 phase. TG study reveals that the nanophosphors are thermally stable. Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy techniques were used to obtain the information about internal and external vibrational modes present in the SrWO4 structure. Optical properties were investigated using UV-vis and photoluminescence (PL) spectroscopy. The average crystallite size was calculated using Debye-Scherrer's for as-prepared and 800 °C annealed samples and is found to be in the range of ∼35-70 nm. The luminescence intensity of Eu3+ doped SrWO4 nanoparticles under 364 nm excitation wavelength reveals that 5D0 → 7F2 transition at ∼613 nm (red) is more prominent than that of 5D0 → 7F1 transition at ∼590 nm (orange). Also upon excitation by UV radiation, the SrWO4:Dy3+ phosphor shows the yellow and blue transition lines appearing at ∼572 and 484 nm which are the characteristic electronic transitions of 4F9/2-6H13/2 and 4F9/2-6H15/2 emission line of Dy3+, respectively. Also Sm3+ doped SrWO4 nanophosphor shows its characteristic emission lines in the range of 550-720 nm, corresponding to 4G5/2 → 6HJ (J = 5/2, 7/2, 9/2 and 11/2) transitions of Sm3+ ions. The predominant orange red color can be attributed to 4G5/2 → 6H9/2 located at ∼642 nm. This is related to the polarizing effect due to the energy transfer from WO42- to the Eu3+, Dy3+ and Sm3+ sites, respectively. Effect of annealing on the photoluminescence properties of samples has been studied and it was found that luminescence intensity increases up to ∼3 times on heating the samples at 800 °C. This may be due to reduction in non-radiative decay channels

  8. NO{sub 2} gas sensing of flame-made Pt-loaded WO{sub 3} thick films

    Energy Technology Data Exchange (ETDEWEB)

    Samerjai, Thanittha [Nanoscience and Nanotechnology Program, Faculty of Graduate School, Chiang Mai University, Chiang Mai 50200 (Thailand); Tamaekong, Nittaya [Program in Materials Science, Faculty of Science, Maejo University, Chiang Mai 50290 (Thailand); Liewhiran, Chaikarn [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Wisitsoraat, Anurat [Nanoelectronics and MEMS Laboratory, National Electronics and Computer Technology Center, Klong Luang, Pathumthani 12120 (Thailand); Phanichphant, Sukon, E-mail: sphanichphant@yahoo.com [Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand)

    2014-06-01

    Unloaded WO{sub 3} and 0.25–1.0 wt% Pt-loaded WO{sub 3} nanoparticles for NO{sub 2} gas detection were synthesized by flame spray pyrolysis (FSP) and characterized via X-ray diffraction (XRD), scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM). The BET surface area (SSA{sub BET}) of the nanoparticles was measured by nitrogen adsorption. The NO{sub 2} sensing properties of the sensors based on unloaded and Pt-loaded WO{sub 3} nanoparticles were investigated. The results showed that the gas sensing properties of the Pt-loaded WO{sub 3} sensors were excellent to those of the unloaded one. Especially, 0.25 wt% Pt-loaded WO{sub 3} sensor showed highest response to NO{sub 2} than the others at low operating temperature of 150 °C. - Graphical abstract: The response of 0.25 wt% Pt-loaded WO3 sensor was 637 towards NO{sub 2} concentration of 10 ppm at 150 °C. - Highlights: • Unloaded and Pt-loaded WO{sub 3} nanoparticles for NO{sub 2} gas detection were synthesized by flame spray pyrolysis (FSP). • Gas sensing properties of the Pt-loaded WO{sub 3} sensors were excellent to those of the unloaded one. • 0.25 wt% Pt-loaded WO{sub 3} sensor showed highest response to NO{sub 2} at low operating temperature of 150 °C.

  9. Study of photocatalytic activities of Bi2WO6 nanoparticles synthesized by fast microwave-assisted method

    International Nuclear Information System (INIS)

    Phu, Nguyen Dang; Hoang, Luc Huy; Chen, Xiang-Bai; Kong, Meng-Hong; Wen, Hua-Chiang; Chou, Wu Ching

    2015-01-01

    We present a study of photocatalytic activities of Bi 2 WO 6 nanoparticles synthesized by fast microwave-assisted method. The photocatalytic activities of the nanoparticles were evaluated by the decolorization of methylene-blue under visible-light-irradiation. Our results show that the surface area of Bi 2 WO 6 nanoparticles plays a major role for improving photocatalytic activity, while visible-light absorption has only a weak effect on photocatalytic activity. This suggests efficient transportation of photo-generated electrons and holes to the oxidation active sites on the surface of nanoparticles, indicating Bi 2 WO 6 nanoparticles synthesized by fast microwave-assisted method are promising for achieving high photocatalytic activity under visible-light-irradiation. - Highlights: • The Bi 2 WO 6 nanoparticles were synthesized via fast microwave-assisted method. • The obtained Bi 2 WO 6 nanoparticles exhibited visible-light absorbance. • The surface area of Bi 2 WO 6 nanoparticles plays major role for improving photocatalytic activity. • The Bi 2 WO 6 nanoparticles are promising for achieving high photocatalytic activity under visible-light-irradiation

  10. Photon mass attenuation coefficients of a silicon resin loaded with WO3, PbO, and Bi2O3 Micro and Nano-particles for radiation shielding

    Science.gov (United States)

    Verdipoor, Khatibeh; Alemi, Abdolali; Mesbahi, Asghar

    2018-06-01

    Novel shielding materials for photons based on silicon resin and WO3, PbO, and Bi2O3 Micro and Nano-particles were designed and their mass attenuation coefficients were calculated using Monte Carlo (MC) method. Using lattice cards in MCNPX code, micro and nanoparticles with sizes of 100 nm and 1 μm was designed inside a silicon resin matrix. Narrow beam geometry was simulated to calculate the attenuation coefficients of samples against mono-energetic beams of Co60 (1.17 and 1.33 MeV), Cs137 (663.8 KeV), and Ba133 (355.9 KeV). The shielding samples made of nanoparticles had higher mass attenuation coefficients, up to 17% relative to those made of microparticles. The superiority of nano-shields relative to micro-shields was dependent on the filler concentration and the energy of photons. PbO, and Bi2O3 nanoparticles showed higher attenuation compared to WO3 nanoparticles in studied energies. Fabrication of novel shielding materials using PbO, and Bi2O3 nanoparticles is recommended for application in radiation protection against photon beams.

  11. A simple synthesis of MnWO{sub 4} nanoparticles as a novel energy storage material

    Energy Technology Data Exchange (ETDEWEB)

    Li, Feihui, E-mail: feihuili2012@163.com [Department of Applied Chemistry, School of Science, Tianjin University of Commerce, Tianjin 300134 (China); Xu, Xiaoyang, E-mail: xiaoyangxu2012@163.com [School of Science, Tianjin University (China); Huo, Jialei; Wang, Wei [School of Chemical Engineering, Tianjin 300072 (China)

    2015-11-01

    MnWO{sub 4} nanoparticles with the shuttle-like shape were prepared by a simple chemical co-precipitation method and analyzed by X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy. The prepared MnWO{sub 4} was used as the electrode material of a supercapacitor, and its electrochemical performance was studied using cyclic voltammetry, galvanostatic charge/discharge cycles and electrochemical impedance spectroscopy. The MnWO{sub 4} exhibited good electrochemical performance. The MnWO{sub 4} nanoparticles had specific capacitances of 295 F/g at a scan rate of 5 mV/s and 219 F/g at a current density of 0.4 A/g. They also showed good cycle-life stability and low resistance. Therefore, MnWO{sub 4} is a promising electrode material for supercapacitors. - Highlights: • The shuttle-like MnWO{sub 4} nanoparticles have been prepared. • The prepared MnWO{sub 4} nanoparticles exhibit good electrochemical performances. • MnWO{sub 4} is a promising electrode material for supercapacitors.

  12. Low-temperature molten salt synthesis and characterization of CoWO4 nano-particles

    International Nuclear Information System (INIS)

    Song Zuwei; Ma Junfeng; Sun Huyuan; Sun Yong; Fang Jingrui; Liu Zhengsen; Gao Chang; Liu Ye; Zhao Jingang

    2009-01-01

    CoWO 4 nano-particles were successfully synthesized at a low temperature of 270 deg. C by a molten salt method, and effects of such processing parameters as holding time and salt quantity on the crystallization and development of CoWO 4 crystallites were initially studied. The products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and photoluminescent spectra techniques (PL), respectively. Experimental results showed that the well-crystallized CoWO 4 nano-particles with ca. 45 nm in diameter could be obtained at 270 deg. C for a holding time of 8 h with 6:1 mass ratio of the salt to CoWO 4 precursor, and XRD analysis evidenced that the as-prepared sample was a pure monoclinic phase of CoWO 4 with wolframite structure. Their PL spectra revealed that the CoWO 4 nano-particles displayed a very strong PL peak at 453 nm with the excitation wavelength of 230 nm, and PL properties of CoWO 4 crystallites relied on their crystalline state, especially on their particle size.

  13. Enhancement of oxidative electrocatalytic properties of platinum nanoparticles by supporting onto mixed WO{sub 3}/ZrO{sub 2} matrix

    Energy Technology Data Exchange (ETDEWEB)

    Rutkowska, Iwona A., E-mail: ilinek@chem.uw.edu.pl; Wadas, Anna; Kulesza, Pawel J., E-mail: pkulesza@chem.uw.edu.pl

    2016-12-01

    Highlights: • The electrocatalytic system utilizing Pt nanoparticles dispersed on mixed metal oxide (WO{sub 3}/ZrO{sub 2}) system is proposed. • The system is characterized by high activity toward oxidations of ethanol, methanol and acetaldehyde in acid medium. • The enhancement effect is facilitated by presence of hydroxyl groups, high mobility of protons and improved distribution of electrons. • Strong interactions between Pt and the mixed oxide WO{sub 3}/ZrO{sub 2} support are postulated. - Abstract: Nanostructured mixed metal (W, Zr) oxide matrices (in a form of layered intercalated films of WO{sub 3} and ZrO{sub 2}) are considered here for supporting and activating catalytic platinum nanoparticles toward electrooxidation of ethanol. Remarkable increases of electrocatalytic (voltammetric, chronoamperometric) currents measured in 0.5 mol dm{sup −3} H{sub 2}SO{sub 4} (containing 0.5 mol dm{sup −3} ethanol) have been observed. Comparison has been made to the behavior of methanol and acetaldehyde under analogous conditions. The enhancement effects are interpreted in terms of specific interactions between platinum nanoparticles and the metal oxide species, high acidity of the mixed oxide sites, as well as high population of surface hydroxyl groups and high mobility of protons existing in close vicinity of Pt catalytic sites. The metal oxide nanostructures are expected to interact competitively (via the surface hydroxyl groups) with adsorbates of the undesirable reaction intermediates, including CO, facilitating their desorption (“third body effect”), or even oxidative removal (e.g., of CO to CO{sub 2}). The fact that the partially reduced tungsten oxide (H{sub x}WO{sub 3}) component is characterized by fast electron transfers coupled to proton displacements tends to improve the overall charge propagation at the electrocatalytic interface.

  14. Faster response of NO2 sensing in graphene–WO3 nanocomposites

    International Nuclear Information System (INIS)

    Srivastava, Shubhda; Jain, Kiran; Gupta, Govind; Senguttuvan, T D; Singh, V N; Singh, Sukhvir; Vijayan, N; Dilawar, Nita

    2012-01-01

    Graphene-based nanocomposites have proven to be very promising materials for gas sensing applications. In this paper, we present a general approach for the preparation of graphene–WO 3 nanocomposites. Graphene–WO 3 nanocomposite thin-layer sensors were prepared by drop coating the dispersed solution onto the alumina substrate. These nanocomposites were used for the detection of NO 2 for the first time. TEM micrographs revealed that WO 3 nanoparticles were well distributed on graphene nanosheets. Three different compositions (0.2, 0.5 and 0.1 wt%) of graphene with WO 3 were used for the gas sensing measurements. It was observed that the sensor response to NO 2 increased nearly three times in the case of graphene–WO 3 nanocomposite layer as compared to a pure WO 3 layer at room temperature. The best response of the graphene–WO 3 nanocomposite was obtained at 250 °C. (paper)

  15. Pronounced effects of the nominal concentrations of WO3 and Ag: WO3 nano-plates (obtained by a co-precipitation method) on their structural, morphological and optical properties

    Science.gov (United States)

    Rajendran, V.; Deepa, B.

    2018-03-01

    Tungsten oxide and different concentration of silver (Ag)-doped tungsten oxide nano material were synthesized by co-precipitation technique. The functional vibrations, structure, and morphology of as-prepared nano material were studied by Fourier transmission infrared spectroscopy, X-ray diffraction, scanning electron microscopy (SEM) and High-resolution transmission electron microscopy (HR-TEM) techniques. The SEM and HR-TEM analysis revealed the formation of nano-plate/nano rods with an average diameter of 40-80 nm diameter and 1-1.5 mm length. Fluorescence (PL) and UV-visible absorption techniques have been used to study the optical properties of the prepared nanoparticles. The observed red shift in the visible absorption spectra confirmed the promoted electron-phonon interaction in WO3 and Ag: WO3 nanoparticles compared to bulk structures. The photoluminescence of nanocrystalline Ag2+ doped WO3 exhibited a strong violet-blue, blue-green emission. Concentration dependence of the emission intensity of Ag2+ in WO3 was studied, and the significant concentration was found to be 0.5% of Ag: WO3. The effluent dye degradation executed for the 0.5% of Ag: WO3 sample under the visible light which reveals the highest degradation efficiency in appropriate time.

  16. Solar photocatalytic activity of TiO2 modified with WO3 on the degradation of an organophosphorus pesticide

    International Nuclear Information System (INIS)

    Ramos-Delgado, N.A.; Gracia-Pinilla, M.A.; Maya-Treviño, L.; Hinojosa-Reyes, L.; Guzman-Mar, J.L.; Hernández-Ramírez, A.

    2013-01-01

    Highlights: • TiO 2 and WO 3 /TiO 2 (2 and 5%) were tested in the photocatalytic malathion degradation. • The use of solar radiation in the photocatalytic degradation process was evaluated. • Modified catalyst showed greater photocatalytic activity than pure TiO 2 . • The mineralization rate was improved when WO 3 content on TiO 2 was 2%. -- Abstract: In this study, the solar photocatalytic activity (SPA) of WO 3 /TiO 2 photocatalysts synthesized by the sol–gel method with two different percentages of WO 3 (2 and 5%wt) was evaluated using malathion as a model contaminant. For comparative purpose bare TiO 2 was also prepared by sol–gel process. The powders were characterized by X-ray diffraction (XRD), Raman spectroscopy, diffuse reflectance UV–vis spectroscopy (DRUV–vis), specific surface area by the BET method (SSA BET ), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM) and scanning transmission electron microscopy with a high annular angle dark field detector (STEM-HAADF). The XRD, Raman, HRTEM and STEM-HAADF analyses indicated that WO 3 was present as a monoclinic crystalline phase with nanometric cluster sizes (1.1 ± 0.1 nm for 2% WO 3 /TiO 2 and 1.35 ± 0.3 nm for 5% WO 3 /TiO 2 ) and uniformly dispersed on the surface of TiO 2 . The particle size of the materials was 19.4 ± 3.3 nm and 25.6 ± 3 nm for 2% and 5% WO 3 /TiO 2 , respectively. The SPA was evaluated on the degradation of commercial malathion pesticide using natural solar light. The 2% WO 3 /TiO 2 photocatalyst exhibited the best photocatalytic activity achieving 76% of total organic carbon (TOC) abatement after 300 min compared to the 5% WO 3 /TiO 2 and bare TiO 2 photocatalysts, which achieved 28 and 47% mineralization, respectively. Finally, experiments were performed to assess 2% WO 3 /TiO 2 catalyst activity on repeated uses; after several successive cycles its photocatalytic activity was retained showing long-term stability

  17. Study of photocatalytic activities of Bi{sub 2}WO{sub 6} nanoparticles synthesized by fast microwave-assisted method

    Energy Technology Data Exchange (ETDEWEB)

    Phu, Nguyen Dang [Faculty of Physics, Hanoi National University of Education, 136 Xuanthuy, Cau Giay, Hanoi (Viet Nam); Hoang, Luc Huy, E-mail: hoanglhsp@hnue.edu.vn [Faculty of Physics, Hanoi National University of Education, 136 Xuanthuy, Cau Giay, Hanoi (Viet Nam); Chen, Xiang-Bai, E-mail: xchen@wit.edu.cn [School of Science and Laboratory of Optical Information Technology, Wuhan Institute of Technology, Wuhan 430205 (China); Kong, Meng-Hong [School of Science and Laboratory of Optical Information Technology, Wuhan Institute of Technology, Wuhan 430205 (China); Wen, Hua-Chiang; Chou, Wu Ching [Department of Electrophysics, National Chiao Tung University, Hsin-Chu 30010, Taiwan (China)

    2015-10-25

    We present a study of photocatalytic activities of Bi{sub 2}WO{sub 6} nanoparticles synthesized by fast microwave-assisted method. The photocatalytic activities of the nanoparticles were evaluated by the decolorization of methylene-blue under visible-light-irradiation. Our results show that the surface area of Bi{sub 2}WO{sub 6} nanoparticles plays a major role for improving photocatalytic activity, while visible-light absorption has only a weak effect on photocatalytic activity. This suggests efficient transportation of photo-generated electrons and holes to the oxidation active sites on the surface of nanoparticles, indicating Bi{sub 2}WO{sub 6} nanoparticles synthesized by fast microwave-assisted method are promising for achieving high photocatalytic activity under visible-light-irradiation. - Highlights: • The Bi{sub 2}WO{sub 6} nanoparticles were synthesized via fast microwave-assisted method. • The obtained Bi{sub 2}WO{sub 6} nanoparticles exhibited visible-light absorbance. • The surface area of Bi{sub 2}WO{sub 6} nanoparticles plays major role for improving photocatalytic activity. • The Bi{sub 2}WO{sub 6} nanoparticles are promising for achieving high photocatalytic activity under visible-light-irradiation.

  18. Ferrocenyl-doped silica nanoparticles as an immobilized affinity support for electrochemical immunoassay of cancer antigen 15-3

    International Nuclear Information System (INIS)

    Hong Chenglin; Yuan Ruo; Chai Yaqin; Zhuo Ying

    2009-01-01

    The aim of this study is to elaborate a simple and sensitive electrochemical immunoassay using ferrocenecarboxylic (Fc-COOH)-doped silica nanoparticles (SNPs) as an immobilized affinity support for cancer antigen 15-3 (CA 15-3) detection. The Fc-COOH-doped SNPs with redox-active were prepared by using a water-in-oil microemulsion method. The use of colloidal silica could prevent the leakage of Fc-COOH and were easily modified with trialkoxysilane reagents for covalent conjugation of CA 15-3 antibodies (anti-CA 15-3). The Fc-COOH-doped SNPs were characterized by X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). The fabrication process of the electrochemical immunosensor was demonstrated by using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) techniques. Under optimal conditions, the developed immunosensor showed good linearity at the studied concentration range of 2.0-240 U mL -1 with a coefficient 0.9986 and a detection limit of 0.64 U mL -1 at S/N = 3

  19. Ferrocenyl-doped silica nanoparticles as an immobilized affinity support for electrochemical immunoassay of cancer antigen 15-3.

    Science.gov (United States)

    Hong, Chenglin; Yuan, Ruo; Chai, Yaqin; Zhuo, Ying

    2009-02-09

    The aim of this study is to elaborate a simple and sensitive electrochemical immunoassay using ferrocenecarboxylic (Fc-COOH)-doped silica nanoparticles (SNPs) as an immobilized affinity support for cancer antigen 15-3 (CA 15-3) detection. The Fc-COOH-doped SNPs with redox-active were prepared by using a water-in-oil microemulsion method. The use of colloidal silica could prevent the leakage of Fc-COOH and were easily modified with trialkoxysilane reagents for covalent conjugation of CA 15-3 antibodies (anti-CA 15-3). The Fc-COOH-doped SNPs were characterized by X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). The fabrication process of the electrochemical immunosensor was demonstrated by using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) techniques. Under optimal conditions, the developed immunosensor showed good linearity at the studied concentration range of 2.0-240 UmL(-1) with a coefficient 0.9986 and a detection limit of 0.64 UmL(-1) at S/N=3.

  20. Highly sensitive electrochemical immunoassay for human IgG using double-encoded magnetic redox-active nanoparticles

    International Nuclear Information System (INIS)

    Tang, D.; Tang, J.; Su, B.; Chen, H.; Chen, G.; Huang, J.

    2010-01-01

    A new sandwich-type electrochemical immunoassay was developed for the detection of human IgG using doubly-encoded and magnetic redox-active nanoparticles as recognition elements on the surface of a glassy carbon electrode modified with anti-IgG on nanogold particles. The recognition elements were synthesized by coating magnetic Fe3O4 nanoparticles with Prussian blue nanoparticles and then covered with peroxidase-labeled anti-IgG antibodies (POx-anti-IgG) on Prussian blue nanoparticles. The immunoelectrode displays very good electrochemical properties towards detection of IgG via using double-encoded magnetic redox-active nanoparticles as trace and hydrogen peroxide as enzyme substrate. Its limit of detection (10 pmol.L -1 ) is 10-fold better than that of using plain POx-anti-IgG secondary antibodies. The method was applied to the detection of IgG in serum samples, and an excellent correspondence with the reference values was found. (author)

  1. Synthesis, strong room-temperature PL and photocatalytic activity of ZnO/ZnWO{sub 4} rod-like nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Validzic, Ivana Lj., E-mail: validzic@vinca.rs [Vinca Institute of Nuclear Sciences, University of Belgrade, P.O. Box 522, 11001 Belgrade (Serbia); Savic, Tatjana D.; Krsmanovic, Radenka M.; Jovanovic, Dragana J.; Novakovic, Mirjana M.; Popovic, Maja C.; Comor, Mirjana I. [Vinca Institute of Nuclear Sciences, University of Belgrade, P.O. Box 522, 11001 Belgrade (Serbia)

    2012-05-25

    Highlights: Black-Right-Pointing-Pointer Novel low temperature method for the synthesis of ZnO/ZnWO{sub 4} rod-like nanoparticles. Black-Right-Pointing-Pointer PL showed strong UV band peaked at 3.30 eV and a visible band at 2.71 and 2.53 eV. Black-Right-Pointing-Pointer Variations of the two PL bands were observed for different excitation wavelengths. Black-Right-Pointing-Pointer Band-gap energies of ZnO/ZnWO{sub 4} nanoparticles were found to be 3.62 and 3.21 eV. Black-Right-Pointing-Pointer Photocatalytic behaviour of ZnO is dependent on the formation of ZnWO{sub 4} phase. - Abstract: Zinc oxide (ZnO)/zinc tungstate (ZnWO{sub 4}) rod-like nanoparticles with diameters in the range of 6-11 nm and length of about 30 nm were synthesized by a low temperature soft solution method at 95 Degree-Sign C in the presence of non-ionic copolymer surfactant. It was found that their crystallinity was enhanced with the increase of heating time from 1 h up to 120 h. The photoluminescence (PL) measurements showed very strong, narrow UV band peaked at 3.30 eV and a broad visible band peaking at 2.71 eV with a shoulder at about 2.53 eV, for {lambda}{sub exc} < 300 nm. Quite large variations in the intensities of the two PL bands were observed for different excitation wavelengths. The intensity of the main visible band decreases with decreasing excitation energy and disappears when samples are excited {lambda} = 320 nm (E{sub exc} = 3.875 eV). We found that observed optical properties originate from ZnO phase. UV band gap PL had high intensity for all applied excitations, probably induced by ZnWO{sub 4} phase presence on the surface. In addition, two values were found for direct band-gap energy of ZnO/ZnWO{sub 4} rod-like nanoparticles 3.62 and 3.21 eV, determined from reflectance spectrum. The photocatalytic behaviour of ZnO is strongly dependent on the formation of ZnWO{sub 4} phase, of the obtained rod-like nanoparticles.

  2. Enhancement of visible-light photocatalytic activity of silver and mesoporous carbon co-modified Bi2WO6

    International Nuclear Information System (INIS)

    Zhao, Qian; Gong, Ming; Liu, Wangping; Mao, Yulin; Le, Shukun; Ju, Shang; Long, Fei; Liu, Xiufang; Liu, Kai; Jiang, Tingshun

    2015-01-01

    Graphical abstract: - Highlights: • Silver and mesoporous carbon co-modified Bi 2 WO 6 (Ag/Bi 2 WO 6 /CMK-3) composite was prepared. • Photocatalytic activity of Bi 2 WO 6 was remarkably enhanced by co-modification of silver and mesoporous carbon. • The degradation rate of MB can reach ca. 95.1% under visible light irradiation. • The Ag/Bi 2 WO 6 /CMK-3 composite has good stability and potential application prospects. - Abstract: Ordered mesoporous carbon CMK-3 was prepared by hard template method using SBA-15 as template, sucrose as carbon source. Flower/sphere-like Bi 2 WO 6 and CMK-3/Bi 2 WO 6 photocatalysts were synthesized by hydrothermal method, and then Ag/Bi 2 WO 6 and Ag/Bi 2 WO 6 /CMK-3 composite photocatalysts were prepared via a photoreduction process. The samples were characterized by XRD, UV–vis, TEM (HR-TEM), SEM, N 2 physical adsorption and PL and their photocatalytic activities were evaluated by the photocatalytic degradation of methylene blue (MB) under visible light irradiation. The results show that both incorporating of CMK-3 and Ag loading greatly improved the photocatalytic activity of Bi 2 WO 6 , and the content of CMK-3 and silver have an impact on the photocatalytic activity of Bi 2 WO 6 . The photocatalytic activity of Ag/Bi 2 WO 6 /CMK-3 photocatalyst is superior to the activities of CMK-3/Bi 2 WO 6 and Ag/Bi 2 WO 6 under comparable conditions, and Ag/Bi 2 WO 6 /CMK-3 photocatalyst has high stability and is easy to be recycled. Also, the mechanism for the enhancement of the photocatalytic activity of CMK-3 and Ag co-modified Bi 2 WO 6 was also investigated

  3. Ultrasensitive electrochemiluminescent immunoassay for morphine using a gold electrode modified with CdS quantum dots, polyamidoamine, and gold nanoparticles

    International Nuclear Information System (INIS)

    Fei, Wenjuan; Chen, Feifei; Sun, Li; Li, Qianhua; Wu, Ying; Yang, Jianping

    2014-01-01

    We report on a novel electrochemiluminescent (ECL) immunoassay for the ultrasensitive determination of morphine by making use of a gold electrode which was modified with a nanocomposite film containing self-assembled polyamidoamine (PAMAM) CdS quantum dots and electrodeposited gold nanoparticles (Au-NPs). The highly uniform and well-dispersed quantum dots were capped with PAMAM dendrimers. Due to the synergistic effect of the modified quantum dots and the electrodeposited Au-NPs, the ECL response is dramatically enhanced. Under optimal experimental conditions, the immunoreaction between morphine and anti-morphine antibody resulted in a decrease of the ECL signal because of steric hindrance. The calibration plot is linear in the morphine concentration range from 0.2 to 180 ng•mL −1 , with a detection limit as low as 67 pg•mL −1 . The sensor was successfully applied to the determination of morphine in blood plasma. This kind of assay is expected to pave new avenues in label-free drug assays. (author)

  4. Tungsten oxide-graphene oxide (WO3-GO) nanocomposite as an efficient photocatalyst, antibacterial and anticancer agent

    Science.gov (United States)

    Jeevitha, G.; Abhinayaa, R.; Mangalaraj, D.; Ponpandian, N.

    2018-05-01

    Functioning of ultrasonically prepared tungsten oxide-graphene oxide (WO3-GO) nanocomposite as a photocatalyst, antibacterial and anticancer system was investigated and the obtained results were compared with that of pure WO3 nanoparticles. Structural, morphological, compositional and optical properties of the prepared WO3 nanoparticles and WO3-GO nanocomposite were studied. Photocatalytic efficiency of the system on organic dyes such as methylene blue (MB, cationic) and indigo carmine (IC, anionic) was investigated. The enhanced efficiency of the WO3-GO nanocomposite system was evaluated under sunlight and compared with that of pure WO3. The degradation efficiency values for MB and IC were found to be 97.03% and 95.43% at 180 and 120 min respectively. Antibacterial activity of the WO3-GO nanocomposite under visible light was tested and improved inhibition results were observed for Escherichia coli and Bacillus subtilis after 6 h of light exposure. The photocatalytic degradation efficiency and antibacterial activity of the WO3-GO nanocomposite are attributed to the improved electron-hole pair separation rate. Investigation on anticancer activity of WO3-GO nanocomposite was tested on human lung cancer (A-549) cell line and the IC50 value was found to be 139.6 ± 4.53 μg/mL. The results obtained in this study may be used as a platform for the development of photocatalysis applications based on WO3-GO nanocomposite.

  5. Solar photocatalytic activity of TiO{sub 2} modified with WO{sub 3} on the degradation of an organophosphorus pesticide

    Energy Technology Data Exchange (ETDEWEB)

    Ramos-Delgado, N.A. [Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, San Nicolás de los Garza, N.L. (Mexico); Gracia-Pinilla, M.A. [Universidad Autónoma de Nuevo León, Facultad de Ciencias Físico-Matemáticas, Av. Universidad, Cd. Universitaria, San Nicolás de los Garza, N.L. (Mexico); Universidad Autónoma de Nuevo León, Centro de Investigación e Innovación en Desarrollo de Ingeniería y Tecnología, PIIT Km 6, Carretera al Aeropuerto, Apodaca, N.L. (Mexico); Maya-Treviño, L.; Hinojosa-Reyes, L.; Guzman-Mar, J.L. [Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, San Nicolás de los Garza, N.L. (Mexico); Hernández-Ramírez, A., E-mail: aracely.hernandezrm@uanl.edu.mx [Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, San Nicolás de los Garza, N.L. (Mexico)

    2013-12-15

    Highlights: • TiO{sub 2} and WO{sub 3}/TiO{sub 2} (2 and 5%) were tested in the photocatalytic malathion degradation. • The use of solar radiation in the photocatalytic degradation process was evaluated. • Modified catalyst showed greater photocatalytic activity than pure TiO{sub 2}. • The mineralization rate was improved when WO{sub 3} content on TiO{sub 2} was 2%. -- Abstract: In this study, the solar photocatalytic activity (SPA) of WO{sub 3}/TiO{sub 2} photocatalysts synthesized by the sol–gel method with two different percentages of WO{sub 3} (2 and 5%wt) was evaluated using malathion as a model contaminant. For comparative purpose bare TiO{sub 2} was also prepared by sol–gel process. The powders were characterized by X-ray diffraction (XRD), Raman spectroscopy, diffuse reflectance UV–vis spectroscopy (DRUV–vis), specific surface area by the BET method (SSA{sub BET}), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM) and scanning transmission electron microscopy with a high annular angle dark field detector (STEM-HAADF). The XRD, Raman, HRTEM and STEM-HAADF analyses indicated that WO{sub 3} was present as a monoclinic crystalline phase with nanometric cluster sizes (1.1 ± 0.1 nm for 2% WO{sub 3}/TiO{sub 2} and 1.35 ± 0.3 nm for 5% WO{sub 3}/TiO{sub 2}) and uniformly dispersed on the surface of TiO{sub 2}. The particle size of the materials was 19.4 ± 3.3 nm and 25.6 ± 3 nm for 2% and 5% WO{sub 3}/TiO{sub 2}, respectively. The SPA was evaluated on the degradation of commercial malathion pesticide using natural solar light. The 2% WO{sub 3}/TiO{sub 2} photocatalyst exhibited the best photocatalytic activity achieving 76% of total organic carbon (TOC) abatement after 300 min compared to the 5% WO{sub 3}/TiO{sub 2} and bare TiO{sub 2} photocatalysts, which achieved 28 and 47% mineralization, respectively. Finally, experiments were performed to assess 2% WO{sub 3}/TiO{sub 2} catalyst activity on

  6. The enhanced alcohol-sensing response of ultrathin WO3 nanoplates

    International Nuclear Information System (INIS)

    Chen Deliang; Hou Xianxiang; Wen Hejing; Wang Yu; Wang Hailong; Zhang Rui; Lu Hongxia; Xu Hongliang; Guan Shaokang; Li Xinjian; Sun Jing; Gao Lian

    2010-01-01

    Chemical sensors based on semiconducting metal oxide nanocrystals are of academic and practical significance in industrial processing and environment-related applications. Novel alcohol response sensors using two-dimensional WO 3 nanoplates as active elements have been investigated in this paper. Single-crystalline WO 3 nanoplates were synthesized through a topochemical approach on the basis of intercalation chemistry (Chen et al 2008 Small 4 1813). The as-obtained WO 3 nanoplate pastes were coated on the surface of an Al 2 O 3 ceramic microtube with four Pt electrodes to measure their alcohol-sensing properties. The results show that the WO 3 nanoplate sensors are highly sensitive to alcohols (e.g., methanol, ethanol, isopropanol and butanol) at moderate operating temperatures (260-360 deg. C). For butanol, the WO 3 nanoplate sensors have a sensitivity of 31 at 2 ppm and 161 at 100 ppm, operating at 300 deg. C. For other alcohols, WO 3 nanoplate sensors also show high sensitivities: 33 for methanol at 300 ppm, 70 for ethanol at 200 ppm, and 75 for isopropanol at 200 ppm. The response and recovery times of the WO 3 nanoplate sensors are less than 15 s for all the test alcohols. A good linear relationship between the sensitivity and alcohol concentrations has been observed in the range of 2-300 ppm, whereas the WO 3 nanoparticle sensors have not shown such a linear relationship. The sensitivities of the WO 3 nanoplate sensors decrease and their response times become short when the operating temperatures increase. The enhanced alcohol-sensing performance could be attributed to the ultrathin platelike morphology, the high crystallinity and the loosely assembling structure of the WO 3 nanoplates, due to the advantages of the effective adsorption and rapid diffusion of the alcohol molecules.

  7. Degradation of malachite green on Pd/WO3 photocatalysts under simulated solar light

    International Nuclear Information System (INIS)

    Liu Yonggang; Ohko, Yoshihisa; Zhang Ruiqin; YangYingnan; Zhang Zhenya

    2010-01-01

    The photocatalytic degradation of malachite green (MG) dye molecules in aqueous solution was investigated by using palladium (Pd) modified tungsten trioxide (WO 3 ) under simulated solar light. The optimum values for Pd content vs. WO 3 and catalyst concentration in solution for MG (5.0 μmol L -1 ) degradation were 0.5 wt.% and 150 mg L -1 , respectively. The MG concentration change followed the pseudo first order kinetics of the Langmuir-Hinshelwood model. Since MG was also degraded under visible light (λ > 470 nm), which was not absorbed by WO 3 , the mechanism involved both the photocatalytic degradation and self-sensitized degradation of MG. Pd modified WO 3 would be useful as an efficient tool for the decolorization of wastewater under solar light.

  8. Three-dimensional Ag{sub 2}O/WO{sub 3}·0.33H{sub 2}O heterostructures for improving photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    He, Xiaoyu [Department of Applied Physics, Chongqing University, Chongqing 400044 (China); Department of Physics and Electronic Engineering, Yangtze Normal University, Chongqing 408100 (China); Hu, Chenguo, E-mail: hucg@cqu.edu.cn [Department of Applied Physics, Chongqing University, Chongqing 400044 (China); Xi, Yi; Zhang, Kaiyou; Hua, Hao [Department of Applied Physics, Chongqing University, Chongqing 400044 (China)

    2014-02-01

    Highlights: • Ag{sub 2}O/WO{sub 3}·0.33H{sub 2}O 3D network heterostructures are prepared via a simple precipitatation method. • Ag{sub 2}O/WO{sub 3}·0.33H{sub 2}O networks exhibit much enhanced photocatalytic activity. • High photocatalytic activity is attributed to its heterostructure and 3D architectures. - Abstract: Three-dimensional Ag{sub 2}O/WO{sub 3}·0.33H{sub 2}O heterostructures were fabricated by loading Ag{sub 2}O nanoparticles on WO{sub 3}·0.33H{sub 2}O 3D networks via a simple chemical precipitation method. The Ag{sub 2}O/WO{sub 3}·0.33H{sub 2}O heterostructures exhibited much enhanced photocatalytic activity for the degradation of methylene blue (MB) under simulated solar light irradiation. The optimal molar ratio of Ag{sub 2}O and WO{sub 3}·0.33H{sub 2}O is 1:2. The outstanding photocatalytic activity of the Ag{sub 2}O/WO{sub 3}·0.33H{sub 2}O can be attributed to its large surface area of the three-dimensional networks, the enhanced sunlight absorption and the prevention of electrons–holes combination from the heterostructures. The experiment result demonstrates that wide band gap semiconductor (WO{sub 3}·0.33H{sub 2}O) modified by narrow band gap metal oxide (Ag{sub 2}O) with 3D architecture will be an effective route to enhance its photocatalytic activity.

  9. Sulfur Nanoparticles Synthesis and Characterization from H2S Gas, Using Novel Biodegradable Iron Chelates in W/O Microemulsion

    Directory of Open Access Journals (Sweden)

    Harle Arti

    2008-01-01

    Full Text Available AbstractSulfur nanoparticles were synthesized from hazardous H2S gas using novel biodegradable iron chelates in w/o microemulsion system. Fe3+–malic acid chelate (0.05 M aqueous solution was studied in w/o microemulsion containing cyclohexane, Triton X-100 andn-hexanol as oil phase, surfactant, co-surfactant, respectively, for catalytic oxidation of H2S gas at ambient conditions of temperature, pressure, and neutral pH. The structural features of sulfur nanoparticles have been characterized by X-ray diffraction (XRD, transmission electron microscope (TEM, energy dispersive spectroscopy (EDS, diffused reflectance infra-red Fourier transform technique, and BET surface area measurements. XRD analysis indicates the presence of α-sulfur. TEM analysis shows that the morphology of sulfur nanoparticles synthesized in w/o microemulsion system is nearly uniform in size (average particle size 10 nm and narrow particle size distribution (in range of 5–15 nm as compared to that in aqueous surfactant systems. The EDS analysis indicated high purity of sulfur (>99%. Moreover, sulfur nanoparticles synthesized in w/o microemulsion system exhibit higher antimicrobial activity (against bacteria, yeast, and fungi than that of colloidal sulfur.

  10. Enhanced Plasmonic Biosensors of Hybrid Gold Nanoparticle-Graphene Oxide-Based Label-Free Immunoassay

    Science.gov (United States)

    Chiu, Nan-Fu; Chen, Chi-Chu; Yang, Cheng-Du; Kao, Yu-Sheng; Wu, Wei-Ren

    2018-05-01

    In this study, we propose a modified gold nanoparticle-graphene oxide sheet (AuNP-GO) nanocomposite to detect two different interactions between proteins and hybrid nanocomposites for use in biomedical applications. GO sheets have high bioaffinity, which facilitates the attachment of biomolecules to carboxyl groups and has led to its use in the development of sensing mechanisms. When GO sheets are decorated with AuNPs, they introduce localized surface plasmon resonance (LSPR) in the resonance energy transfer of spectral changes. Our results suggest a promising future for AuNP-GO-based label-free immunoassays to detect disease biomarkers and rapidly diagnose infectious diseases. The results showed the detection of antiBSA in 10 ng/ml of hCG non-specific interfering protein with dynamic responses ranging from 1.45 nM to 145 fM, and a LOD of 145 fM. Considering the wide range of potential applications of GO sheets as a host material for a variety of nanoparticles, the approach developed here may be beneficial for the future integration of nanoparticles with GO nanosheets for blood sensing. The excellent anti-interference characteristics allow for the use of the biosensor in clinical analysis and point-of-care testing (POCT) diagnostics of rapid immunoassay products, and it may also be a potential tool for the measurement of biomarkers in human serum.

  11. Silver loaded WO3−x/TiO2 composite multifunctional thin films

    International Nuclear Information System (INIS)

    Dunnill, Charles W.; Noimark, Sacha; Parkin, Ivan P.

    2012-01-01

    Multifunctional WO 3−x –TiO 2 composite thin films have been prepared by sol–gel synthesis and shown to be good visible light photocatalysts whilst retaining a desirable underlying blue colouration. The WO 3−x –TiO 2 composite thin films were further enhanced using silver nanoparticles synthesised in-situ on the surface from the photo-degradation of silver nitrate solution. Thin films were characterised using X-ray diffraction, Raman, Scanning electron microscopy and UV–visible spectroscopy and shown to photo degrade stearic acid, using white light λ = 420–800 nm. - Highlights: ► WO 3−X TiO 2 composite thin films were synthesised by sol–gel methods. ► Blue tinted glass is desirable for the value added glass industry. ► Silver nanoparticle island formation enhances the activity of the films. ► Blue tinted “value added” coated glass is now possible.

  12. Combustion synthesized hierarchically porous WO{sub 3} for selective acetone sensing

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Chengjun; Liu, Xu; Guan, Hongtao; Chen, Gang; Xiao, Xuechun [Department of Materials Science and Engineering, Yunnan University, 650091, Kunming (China); Djerdj, Igor [Ruđer Bošković Institute, Bijenička 54, 10000, Zagreb (Croatia); Wang, Yude, E-mail: ydwang@ynu.edu.cn [Department of Materials Science and Engineering, Yunnan University, 650091, Kunming (China); Yunnan Province Key Lab of Mico-Nano Materials and Technology, Yunnan University, 650091, Kunming (China)

    2016-12-01

    An easy, inexpensive combustion route was designed to synthesize hierarchically porous WO{sub 3}. The tungsten source was fresh peroxiotungstic acid by dissolving tungsten powder into hydrogen peroxide. To promote the combustion reaction, a combined fuel of both glycine and hydrazine hydrate was used. The microstructure was well-connected pores comprised of subunit nanoparticles. Upon exposing towards acetone gas, the porous WO{sub 3} based sensor exhibits high gas response, rapid response and recovery, and good selectivity in the range of 5–1000 ppm under working temperature of 300 °C. This excellent sensing performance was plausibly attributed to the porous morphology, which hence provides more active sites for the gas molecules' reaction. - Graphical abstract: Hierarchically porous WO{sub 3} synthesized by combustion process exhibits high gas response, rapid response and recovery, and excellent selectivity for acetone, making it to be promising candidates for practical detectors for acetone. - Highlights: • Hierarchically porous WO{sub 3} synthesized by combustion process. • Hierarchically porous WO{sub 3} exhibits high gas response and excellent selectivity for acetone. • The excellent sensing property was plausibly attributed to the porous morphology.

  13. Detection of alpha-fetoprotein in magnetic immunoassay of thin channels using biofunctional nanoparticles

    Science.gov (United States)

    Tsai, H. Y.; Gao, B. Z.; Yang, S. F.; Li, C. S.; Fuh, C. Bor

    2014-01-01

    This paper presents the use of fluorescent biofunctional nanoparticles (10-30 nm) to detect alpha-fetoprotein (AFP) in a thin-channel magnetic immunoassay. We used an AFP model biomarker and s-shaped deposition zones to test the proposed detection method. The results show that the detection using fluorescent biofunctional nanoparticle has a higher throughput than that of functional microparticle used in previous experiments on affinity reactions. The proposed method takes about 3 min (versus 150 min of previous method) to detect 100 samples. The proposed method is useful for screening biomarkers in clinical applications, and can reduce the run time for sandwich immunoassays to less than 20 min. The detection limits (0.06 pg/ml) and linear ranges (0.068 pg/ml-0.68 ng/ml) of AFP using fluorescent biofunctional nanoparticles are the same as those of using functional microparticles within experimental errors. This detection limit is substantially lower and the linear range is considerably wider than those of enzyme-linked immunosorbent assay (ELISA) and other methods in sandwich immunoassay methods. The differences between this method and an ELISA in AFP measurements of serum samples were less than 12 %. The proposed method provides simple, fast, and sensitive detection with a high throughput for biomarkers.

  14. Effect of Post-annealing on the Electrochromic Properties of Layer-by-Layer Arrangement FTO-WO3-Ag-WO3-Ag

    Science.gov (United States)

    Hoseinzadeh, S.; Ghasemiasl, R.; Bahari, A.; Ramezani, A. H.

    2018-03-01

    In the current study, composites of tungsten trioxide (W03) and silver (Ag) are deposited in a layer-by-layer electrochromic (EC) arrangement onto a fluorine-doped tin oxide coated glass substrate. Tungsten oxide nanoparticles are an n-type semiconductor that can be used as EC cathode material. Nano-sized silver is a metal that can serve as an electron trap center that facilitates charge departure. In this method, the WO3 and Ag nanoparticle powder were deposited by physical vapor deposition onto the glass substrate. The fabricated electrochromic devices (ECD) were post-annealed to examine the effect of temperature on their EC properties. The morphology of the thin film was characterized by scanning electron microscopy and atomic force microscopy. Structural analysis showed that the addition of silver dopant increased the size of the aggregation of the film. The film had an average approximate roughness of about 17.8 nm. The electro-optical properties of the thin film were investigated using cyclic voltammetry and UV-visible spectroscopy to compare the effects of different post-annealing temperatures. The ECD showed that annealing at 200°C provided better conductivity (maximum current of about 90 mA in the oxidation state) and change of transmittance (ΔT = 90% at the continuous switching step) than did the other thin films. The optical band gaps of the thin film showed that it allowed direct transition at 3.85 eV. The EC properties of these combinations of coloration efficiency and response time indicate that the WO3-Ag-WO3-Ag arrangement is a promising candidate for use in such ECDs.

  15. Silver loaded WO{sub 3-x}/TiO{sub 2} composite multifunctional thin films

    Energy Technology Data Exchange (ETDEWEB)

    Dunnill, Charles W.; Noimark, Sacha; Parkin, Ivan P., E-mail: I.P.Parkin@ucl.ac.uk

    2012-06-30

    Multifunctional WO{sub 3-x}-TiO{sub 2} composite thin films have been prepared by sol-gel synthesis and shown to be good visible light photocatalysts whilst retaining a desirable underlying blue colouration. The WO{sub 3-x}-TiO{sub 2} composite thin films were further enhanced using silver nanoparticles synthesised in-situ on the surface from the photo-degradation of silver nitrate solution. Thin films were characterised using X-ray diffraction, Raman, Scanning electron microscopy and UV-visible spectroscopy and shown to photo degrade stearic acid, using white light {lambda} = 420-800 nm. - Highlights: Black-Right-Pointing-Pointer WO{sub 3-X} TiO{sub 2} composite thin films were synthesised by sol-gel methods. Black-Right-Pointing-Pointer Blue tinted glass is desirable for the value added glass industry. Black-Right-Pointing-Pointer Silver nanoparticle island formation enhances the activity of the films. Black-Right-Pointing-Pointer Blue tinted 'value added' coated glass is now possible.

  16. Porous three-dimensional reduced graphene oxide merged with WO3 for efficient removal of radioactive strontium

    Science.gov (United States)

    Mu, Wanjun; Yu, Qianghong; Hu, rui; Li, Xingliang; Wei, Hongyuan; Jian, Yuan

    2017-11-01

    A simple hydrothermal method was used to prepare 3D nanostructured composite adsorbents of reduced graphene oxide (RGO) and WO3 (RGO/WO3). The analysis results suggest that it possesses a mesoporous 3D structure, in which WO3 nanorods are uniformly loaded on the surface of the RGO. Combining the benefits of GO and WO3, the composites exhibit a higher adsorption capacity for removing Sr2+ from aqueous solutions over a wide pH range (4-11). Adsorption isotherms show that the data fit the Langmuir isotherms well (R > 0.99), and the maximum adsorption capacity of 149.56 mg g-1 was achieved, much higher than that for GO, WO3 and other similar adsorbents. Sr2+ adsorption on RGO/WO3 reached equilibrium within 200 min. The fast adsorption and high adsorption rate of RGO/WO3 are mostly attributable to the plentiful adsorption sites provided by the dispersed WO3 nanoparticles on the RGO surface. Furthermore, the existence of Na+ ions has no obvious effect on the removal of Sr2+ ions by RGO/WO3, and RGO/WO3 adsorbent can be repeated at least 5 times without significant loss of adsorption capacity by adsorption-desorption experiment. Thus, RGO/WO3 shows the potential ability for removal of 90Sr from radioactive wastewater.

  17. Sonochemical synthesis of (3-aminopropyl)triethoxysilane-modified monodispersed silica nanoparticles for protein immobilization

    International Nuclear Information System (INIS)

    Shen, Shou-Cang; Ng, Wai Kiong; Chia, Leonard; Dong, Yuan-Cai; Tan, Reginald B.H.

    2011-01-01

    Graphical abstract: 3-Aminopropyltriethoxysilane modified monodispersed silica nanoparticles were synthesized by rapid sonochemical co-condensation to achieve high capability for protein immobilization. Highlights: → Amino-modified monodispersed silica nanoparticles were synthesized by rapid co-condensation. → Strong positive charge was created by aminopropyl-modification. → Capability for immobilization of negatively charged protein was enhanced. → Electrostatic interaction between proteins and surface contributed to the enhanced adsorption. -- Abstract: 3-Aminopropyltriethoxysilane modified monodispersed silica nanoparticles were synthesized by a rapid sonochemical co-condensation synthesis procedure. The chemical nature of surface organic modifier on the obtained modified silica nanoparticle was characterized by 13 C and 29 Si MAS Nuclear Magnetic Resonance (NMR) spectroscopies, Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA)- differential scanning calorimetry (DSC). Due to the strengthened positive surface charge of the silica nanoparticles by the modification with aminopropyl groups, the capability for bovine serum albumin (BSA) adsorption was significantly increased as compared with bare silica nanoparticles. 80 mg/g BSA was adsorbed on modified silica nanoparticles, whereas only 20 mg/g BSA could be loaded on pure silica nanoparticles. The enhanced positive surface charge repelled proteins with net positive charge and the modified silica nanoparticles exhibited negligible adsorption of lysozyme, thus a selective adsorption of proteins could be achieved.

  18. Sonochemical synthesis of (3-aminopropyl)triethoxysilane-modified monodispersed silica nanoparticles for protein immobilization

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Shou-Cang, E-mail: shen_shoucang@ices.a-star.edu.sg [Institute of Chemical and Engineering Sciences, A-STAR (Agency for Science, Technology and Research), 1 Pesek Road, Jurong Island, Singapore 627833 (Singapore); Ng, Wai Kiong; Chia, Leonard; Dong, Yuan-Cai [Institute of Chemical and Engineering Sciences, A-STAR (Agency for Science, Technology and Research), 1 Pesek Road, Jurong Island, Singapore 627833 (Singapore); Tan, Reginald B.H., E-mail: reginald_tan@ices.a-star.edu.sg [Institute of Chemical and Engineering Sciences, A-STAR (Agency for Science, Technology and Research), 1 Pesek Road, Jurong Island, Singapore 627833 (Singapore); Department of Chemical and Biomolecular Engineering, The National University of Singapore, 4 Engineering Drive 4, Singapore 117576 (Singapore)

    2011-10-15

    Graphical abstract: 3-Aminopropyltriethoxysilane modified monodispersed silica nanoparticles were synthesized by rapid sonochemical co-condensation to achieve high capability for protein immobilization. Highlights: {yields} Amino-modified monodispersed silica nanoparticles were synthesized by rapid co-condensation. {yields} Strong positive charge was created by aminopropyl-modification. {yields} Capability for immobilization of negatively charged protein was enhanced. {yields} Electrostatic interaction between proteins and surface contributed to the enhanced adsorption. -- Abstract: 3-Aminopropyltriethoxysilane modified monodispersed silica nanoparticles were synthesized by a rapid sonochemical co-condensation synthesis procedure. The chemical nature of surface organic modifier on the obtained modified silica nanoparticle was characterized by {sup 13}C and {sup 29}Si MAS Nuclear Magnetic Resonance (NMR) spectroscopies, Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA)- differential scanning calorimetry (DSC). Due to the strengthened positive surface charge of the silica nanoparticles by the modification with aminopropyl groups, the capability for bovine serum albumin (BSA) adsorption was significantly increased as compared with bare silica nanoparticles. 80 mg/g BSA was adsorbed on modified silica nanoparticles, whereas only 20 mg/g BSA could be loaded on pure silica nanoparticles. The enhanced positive surface charge repelled proteins with net positive charge and the modified silica nanoparticles exhibited negligible adsorption of lysozyme, thus a selective adsorption of proteins could be achieved.

  19. A Resistive Humidity Sensor Based on Nanostructured WO3-ZnO Composites

    Directory of Open Access Journals (Sweden)

    Karunesh Tiwari

    2011-11-01

    Full Text Available Paper reports morphological and humidity sensing studies of WO3 and WO3-ZnO composite pellets prepared in the weight % ratio of 10:1, 4:1 and 2:1 by solid-state reaction route. The pellets have been annealed at temperatures of 300-500 °C. XRD pattern shows peaks of ZnWO4 formed due to solid state reaction between WO3 and ZnO. SEM micrographs show that the sensing elements manifest porous structure. Granulation and tendency to agglomerate seen in the SEM micrograph are due to the presence of zinc ions in ZnWO4. Nanoparticles are having their sizes in the range 37-182 nm. The average Kelvin radius at 20˚C room temperature is 27 Ả. Humidity sensing application of the pellets has been studied in a humidity control cabinet. It is observed that as relative humidity increases, there is decrease in the resistance of pellets in the range 10-85 % RH. Sensing element of WO3-ZnO in 2:1 weight % ratio shows best results in 10-85 % relative humidity range. The average sensitivity of this sample is 1.25 MΩ/%RH. This sensing element shows good reproducibility, low hysteresis and less effect of aging.

  20. Improved electrochromical properties of sol-gel WO3 thin films by doping gold nanocrystals

    International Nuclear Information System (INIS)

    Naseri, N.; Azimirad, R.; Akhavan, O.; Moshfegh, A.Z.

    2010-01-01

    In this investigation, the effect of gold nanocrystals on the electrochromical properties of sol-gel Au doped WO 3 thin films has been studied. The Au-WO 3 thin films were dip-coated on both glass and indium tin oxide coated conducting glass substrates with various gold concentrations of 0, 3.2 and 6.4 mol%. Optical properties of the samples were studied by UV-visible spectrophotometry in a range of 300-1100 nm. The optical density spectra of the films showed the formation of gold nanoparticles in the films. The optical bandgap energy of Au-WO 3 films decreased with increasing the Au concentration. Crystalline structure of the doped films was investigated by X-ray diffractometry, which indicated formation of gold nanocrystals in amorphous WO 3 thin films. X-ray photoelectron spectroscopy (XPS) was used to study the surface chemical composition of the samples. XPS analysis indicated the presence of gold in metallic state and the formation of stoichiometric WO 3 . The electrochromic properties of the Au-WO 3 samples were also characterized using lithium-based electrolyte. It was found that doping of Au nanocrystals in WO 3 thin films improved the coloration time of the layer. In addition, it was shown that variation of Au concentration led to color change in the colored state of the Au-WO 3 thin films.

  1. Morphology-controlled synthesis of CdWO4 nanorods and nanoparticles via a molten salt method

    International Nuclear Information System (INIS)

    Wang Yonggang; Ma Junfeng; Tao Jiantao; Zhu Xiaoyi; Zhou Jun; Zhao Zhongqiang; Xie Lijin; Tian Hua

    2006-01-01

    Cadmium tungstate (CdWO 4 ) nanoparticles and nanorods have been successfully synthesized by a molten salt method at 270 deg. C, and the morphology of the nanocrystals can be controlled by adjusting such reaction conditions as the calcined time and the weight ratio of the salt to the CdWO 4 precursor. The resultant sample is a pure phase of CdWO 4 without any other impurities

  2. Synthesis of Bi2WO6 nanoparticles and its electrochemical properties in different electrolytes for pseudocapacitor electrodes

    International Nuclear Information System (INIS)

    Nithya, V.D.; Kalai Selvan, R.; Kalpana, D.; Vasylechko, Leonid; Sanjeeviraja, C.

    2013-01-01

    Highlights: • A simple, economical and environmentally benign sonochemical technique was utilized for the synthesis of homogeneous Bi 2 WO 6 nanoparticles. • This is the first attempt to employ Bi 2 WO 6 as a supercapacitor electrode material. • Effect of electrolyte on the capacitive behaviour of the material is studied. • Bi 2 WO 6 displays good capacitive behaviour in 1 M KOH compared with 1 M NaOH and 1 M LiOH and possess sufficient capacity retention. • It presented an energy density of 67 Wh/kg in the potential range from −0.9 V to 0.1 V and it would be a promising negative electrode for supercapacitor. -- Abstract: Nanosized Bi 2 WO 6 particles were successfully synthesized by sonochemical method with an objective to develop an inexpensive and eco-friendly electrode material for supercapacitors. The prepared material was subjected to various thermal, structural, morphological, compositional, electrical and electrochemical studies. Bi 2 WO 6 nanoparticle with homogeneous distribution was achieved through sonochemical process. The lattice parameter and atomic positions of Bi 2 WO 6 structure were refined through Reitveld analysis. The electrochemical performance of Bi 2 WO 6 nanoparticles was investigated in various aqueous electrolytes such as 1 M NaOH, 1 M LiOH, 1 M Na 2 SO 4 , 1 M KOH and 6 M KOH solutions. Among these, the material exhibited an enhanced electrochemical performance in KOH electrolyte due to its smaller hydration sphere radius, high ionic mobility and lower equivalent series resistance. The charge–discharge studies rendered a specific capacitance of 608 F/g in 1 M KOH at a current density of 0.5 mA/cm 2 . Bi 2 WO 6 exhibited an excellent coulombic efficiency and specific capacitance of around 304 F/g at 3 mA/cm 2 in the potential range from −0.9 to 0.1 V vs Hg/HgO in 1 M KOH electrolyte. The above results assured that Bi 2 WO 6 could be utilized as suitable negative electrode material for supercapacitor applications and 1 M

  3. Highly efficient perovskite solar cells based on a nanostructured WO3-TiO2 core-shell electron transporting material

    KAUST Repository

    Mahmood, Khalid; Swain, Bhabani Sankar; Kirmani, Ahmad R.; Amassian, Aram

    2015-01-01

    Until recently, only mesoporous TiO2 and ZnO were successfully demonstrated as electron transport layers (ETL) alongside the reports of ZrO2 and Al2O3 as scaffold materials in organometal halide perovskite solar cells, largely owing to ease of processing and to high power conversion efficiency. In this article, we explore tungsten trioxide (WO3)-based nanostructured and porous ETL materials directly grown hydrothermally with different morphologies such as nanoparticles, nanorods and nanosheet arrays. The nanostructure morphology strongly influences the photocurrent and efficiency in organometal halide perovskite solar cells. We find that the perovskite solar cells based on WO3 nanosheet arrays yield significantly enhanced photovoltaic performance as compared to nanoparticles and nanorod arrays due to good perovskite absorber infiltration in the porous scaffold and more rapid carrier transport. We further demonstrate that treating the WO3 nanostructures with an aqueous solution of TiCl4 reduces charge recombination at the perovskite/WO3 interface, resulting in the highest power conversion efficiency of 11.24% for devices based on WO3 nanosheet arrays. The successful demonstration of alternative ETL materials and nanostructures based on WO3 will open up new opportunities in the development of highly efficient perovskite solar cells. This journal is © The Royal Society of Chemistry 2015.

  4. Photoelectrochemical detection of enzymatically generated CdS nanoparticles: Application to development of immunoassay.

    Science.gov (United States)

    Barroso, Javier; Saa, Laura; Grinyte, Ruta; Pavlov, Valeri

    2016-03-15

    We report an innovative photoelectrochemical process (PEC) based on graphite electrode modified with electroactive polyvinylpyridine bearing osmium complex (Os-PVP). The system relies on the in situ enzymatic generation of CdS quantum dots (QDs). Alkaline phosphatase (ALP) catalyzes the hydrolisis of sodium thiophosphate (TP) to hydrogen sulfide (H2S) which in the presence Cd(2+) ions yields CdS semiconductor nanoparticles (SNPs). Irradiation of SNPs with the standard laboratory UV-illuminator (wavelength of 365 nm) results in photooxidation of 1-thioglycerol (TG) mediated by Os-PVP complex on the surface of graphite electrode at applied potential of 0.31 V vs. Ag/AgCl. A novel immunoassay based on specific enzyme linked immunosorbent assay (ELISA) combined with the PEC methodology was developed. Having selected the affinity interaction between bovine serum albumine (BSA) with anti-BSA antibody (AB) as a model system, we built the PEC immunoassay for AB. The new assay displays a linear range up to 20 ngmL(-1) and a detection limit (DL) of 2 ngmL(-1) (S/N=3) which is lower 5 times that of the traditional chromogenic ELISA test employing p-nitro-phenyl phosphate (pNPP). Copyright © 2015 Elsevier B.V. All rights reserved.

  5. One-dimensional Z-scheme TiO{sub 2}/WO{sub 3}/Pt heterostructures for enhanced hydrogen generation

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Hongqing [School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001 (China); State Centre for International Cooperation on Designer Low-carbon and Environmental Materials (SCICDLCEM), Zhengzhou University, Zhengzhou 450001, Henan (China); Zhang, Peng, E-mail: Zhangp@zzu.edu.cn [School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001 (China); State Centre for International Cooperation on Designer Low-carbon and Environmental Materials (SCICDLCEM), Zhengzhou University, Zhengzhou 450001, Henan (China); Hu, Junhua, E-mail: Hujh@zzu.edu.cn [School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001 (China); State Centre for International Cooperation on Designer Low-carbon and Environmental Materials (SCICDLCEM), Zhengzhou University, Zhengzhou 450001, Henan (China); Pan, Jimin [School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001 (China); Fan, Jiajie [School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001 (China); State Centre for International Cooperation on Designer Low-carbon and Environmental Materials (SCICDLCEM), Zhengzhou University, Zhengzhou 450001, Henan (China); Shao, Guosheng [School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001 (China); State Centre for International Cooperation on Designer Low-carbon and Environmental Materials (SCICDLCEM), Zhengzhou University, Zhengzhou 450001, Henan (China); Institute for Renewable Energy and Environmental Technologies, University of Bolton, Bolton BL35AB (United Kingdom)

    2017-01-01

    Graphical abstract: We reported one-dimensional solid-state Z-scheme photosynthetic heterojunction system with Pt nanoparticle as an electron collector and WO{sub 3} as a hole collector, leading to effective charge separation. - Highlights: • The composite nanofibers were fabricated by facile electrospinning technique. • The composite nanofibers exhibited enhanced activity for H{sub 2} evolution. • Enhanced activity is due to the formation of Z-scheme TiO{sub 2}/WO{sub 3}/Pt heterojunction. - Abstract: One-dimensional Z-scheme TiO{sub 2}/WO{sub 3}/Pt heterostructures were fabricated by integrating a facile electrospinning technique and subsequent annealing in air. X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and UV–vis diffuse reflectance spectroscopy, were used to characterize the as-fabricated samples. The results showed that the H{sub 2}-generation of the as-fabricated one-dimensional Z-scheme TiO{sub 2}/WO{sub 3}/Pt heterostructures (S2) was greatly enhanced compared with pure TiO{sub 2} nanofibers (S0) and TiO{sub 2}/WO{sub 3} nanofibers (S1). The enhanced photocatalyst activities were mainly attributed to the solid-state Z-scheme photosynthetic heterojunction system with Pt nanoparticle as an electron collector and WO{sub 3} as a hole collector, leading to effective charge separation on these semiconductors, which were evidenced by electrochemical impedance spectroscopy (EIS) and photocurrent analysis.

  6. Comparison of infrared-excited up-converting phosphors and europium nanoparticles as labels in a two-site immunoassay

    International Nuclear Information System (INIS)

    Ukonaho, Telle; Rantanen, Terhi; Jaemsen, Laura; Kuningas, Katri; Paekkilae, Henna; Loevgren, Timo; Soukka, Tero

    2007-01-01

    Research in the field of immunoassays and labels used in the detection has been recently focused on particulate reporters, which possess very high specific activity that excludes the label as a sensitivity limiting factor. However, the large size and shape of the particulate labels may produce additional problems to immunoassay performance. The aim of this work was to study with two identical non-competitive two-site immunoassays whether up-converting phosphor (UCP) particles are comparable in performance with europium(III) chelate-dyed nanoparticles as particulate labels. In addition we strived to verify the common assumption of the photostability of up-converting phosphor particles supporting their potential applicability in imaging. Detection limits in two-site immunoassay for free prostate-specific antigen (free-PSA) were 0.53 ng L -1 and 1.3 ng L -1 using two different up-converting phosphors and 0.16 ng L -1 using europium(III) nanoparticle. Large size distribution and non-specific binding of up-converting phosphor particles caused assay variation in low analyte concentrations and limited the analytical detection limit. The non-specific binding was the major factor limiting the analytical sensitivity of the immunoassay. The results suggests the need for nanoscaled and uniformely sized UCP-particles to increace the sensitivity and applicability of up-converting phosphor particles. Anti-Stokes photoluminescence of up-converting phosphor particles did not photobleach when measured repeatedly, on the contrary, the time-resolved fluorescence of europium nanoparticles photobleached relatively rapidly

  7. Electronic-level interactions of tungsten oxide with unsupported Se/Ru electrocatalytic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Lewera, Adam; Miecznikowski, Krzysztof [Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw (Poland); Hunger, Ralf [Institute of Materials Science, Darmstadt University of Technology, Darmstadt (Germany); Kolary-Zurowska, Aneta [Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw (Poland); Wieckowski, Andrzej [Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL (United States); Kulesza, Pawel J., E-mail: pkulesza@chem.uw.edu.p [Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw (Poland)

    2010-11-01

    Se/Ru nanoparticles - a potent non-platinum catalyst towards oxygen reduction reaction - were modified by hydrated WO{sub 3} and investigated using the rotating disk/ring electrode methods and by synchrotron X-ray photoelectron spectroscopy. The modification resulted in an enhanced catalytic activity towards oxygen reduction reaction (ORR). Our data indicate that the oxygen reduction current starts ca. 70 mV more positive and formation of undesirable hydrogen peroxide has significantly decreased following the modification of Se/Ru with WO{sub 3}. X-ray photoelectron spectroscopy reveals that WO{sub 3} interacts electronically with Se/Ru as the W 4f and Se 3d line-shapes change. We therefore conclude that the electronic interactions between Se/Ru and WO{sub 3} are primarily responsible for the increase in activity and selectivity of the WO{sub 3}-modified Se/Ru towards ORR.

  8. Electronic-level interactions of tungsten oxide with unsupported Se/Ru electrocatalytic nanoparticles

    International Nuclear Information System (INIS)

    Lewera, Adam; Miecznikowski, Krzysztof; Hunger, Ralf; Kolary-Zurowska, Aneta; Wieckowski, Andrzej; Kulesza, Pawel J.

    2010-01-01

    Se/Ru nanoparticles - a potent non-platinum catalyst towards oxygen reduction reaction - were modified by hydrated WO 3 and investigated using the rotating disk/ring electrode methods and by synchrotron X-ray photoelectron spectroscopy. The modification resulted in an enhanced catalytic activity towards oxygen reduction reaction (ORR). Our data indicate that the oxygen reduction current starts ca. 70 mV more positive and formation of undesirable hydrogen peroxide has significantly decreased following the modification of Se/Ru with WO 3 . X-ray photoelectron spectroscopy reveals that WO 3 interacts electronically with Se/Ru as the W 4f and Se 3d line-shapes change. We therefore conclude that the electronic interactions between Se/Ru and WO 3 are primarily responsible for the increase in activity and selectivity of the WO 3 -modified Se/Ru towards ORR.

  9. Pt supported self-assembled nest-like-porous WO3 hierarchical microspheres as electrocatalyst for methanol oxidation

    International Nuclear Information System (INIS)

    Zhang, Jun; Tu, Jiang-ping; Du, Gao-hui; Dong, Zi-min; Su, Qing-mei; Xie, Dong; Wang, Xiu-li

    2013-01-01

    Highlights: ► Nest-like-porous (NLP) WO 3 microspheres are assembled by a hydrothermal method. ► The NLP-WO 3 microspheres have a hexagonal structure and high porous surface. ► Great enhancement of electrochemical property is achieved for Pt/NLP-WO 3 microspheres. -- Abstract: Hexagonal tungsten trioxide (hex-WO 3 ) hierarchical microspheres with nest-like pores are synthesized by a facile hydrothermal method. The nest-like-porous (NLP) WO 3 hierarchical microspheres with 5–6 μm in diameters are self-assembled of single-crystal nanowires. The nanowires have lengths of several hundred nanometers and diameters of 5–30 nm; the long axis of nanowire is oriented toward 〈0 0 1〉 direction. The specific surface area of hex-WO 3 microspheres is 62 m 2 g −1 . 20 wt.% Pt nanoparticles with ∼7 nm are loaded onto the WO 3 microspheres using a conventional microwave-assisted ethylene glycol (EG) method. The electrocatalytic activity for methanol oxidation of Pt/NLP-WO 3 microspheres is investigated by cyclic voltammetry and chronoamperometry. Due to the large tunnels of hexagonal structure and high porous surface morphology, great enhancement of electrochemical performance is achieved. The Pt/NLP-WO 3 microspheres are demonstrated to be a promising anode material for direct methanol fuel cells (DMFC)

  10. Visible-light activate Ag/WO3 films based on wood with enhanced negative oxygen ions production properties

    Science.gov (United States)

    Gao, Likun; Gan, Wentao; Cao, Guoliang; Zhan, Xianxu; Qiang, Tiangang; Li, Jian

    2017-12-01

    The Ag/WO3-wood was fabricated through a hydrothermal method and a silver mirror reaction. The system of visible-light activate Ag/WO3-wood was used to produce negative oxygen ions, and the effect of Ag nanoparticles on negative oxygen ions production was investigated. From the results of negative oxygen ions production tests, it can be observed that the sample doped with Ag nanoparticles, the concentration of negative oxygen ions is up to 1660 ions/cm3 after 60 min visible light irradiation. Moreover, for the Ag/WO3-wood, even after 60 min without irradiation, the concentration of negative oxygen ions could keep more than 1000 ions/cm3, which is up to the standard of the fresh air. Moreover, due to the porous structure of wood, the wood acted as substrate could promote the nucleation of nanoparticles, prevent the agglomeration of the particles, and thus lead the improvement of photocatalytic properties. And such wood-based functional materials with the property of negative oxygen ions production could be one of the most promising materials in the application of indoor decoration materials, which would meet people's pursuit of healthy, environment-friendly life.

  11. Ultrasmall, water dispersible, TWEEN80 modified Yb:Er:NaGd(WO4)2 nanoparticles with record upconversion ratiometric thermal sensitivity and their internalization by mesenchymal stem cells

    Science.gov (United States)

    Cascales, Concepción; Paíno, Carlos L.; Bazán, Eulalia; Zaldo, Carlos

    2017-05-01

    This work presents the synthesis by coprecipitation of diamond shaped Yb:Er:NaGd(WO4)2 crystalline nanoparticles (NPs) with diagonal dimensions in the 5-7 nm × 10-12 nm range which have been modified with TWEEN80 for their dispersion in water, and their interaction with mesenchymal stem cells (MSCs) proposed as cellular NP vehicles. These NPs belong to a large family of tetragonal Yb:Er:NaT(XO4)2 (T = Y, La, Gd, Lu; X = Mo, W) compounds with green (2H11/2 + 4S3/2 → 4I15/2) Er-related upconversion (UC) efficiency comparable to that of Yb:Er:β-NaYF4 reference compound, but with a ratiometric thermal sensitivity (S) 2.5-3.5 times larger than that of the fluoride. At the temperature range of interest for biomedical applications (˜293-317 K/20-44 °C) S = 108-118 × 10-4 K-1 for 20 at%Yb:5 at%Er:NaGd(WO4)2 NPs, being the largest values so far reported using the 2H11/2/4S3/2 Er intensity ratiometric method. Cultured MSCs, incubated with these water NP emulsions, internalize and accumulate the NPs enclosed in endosomes/lysosomes. Incubations with up to 10 μg of NPs per ml of culture medium maintain cellular metabolism at 72 h. A thermal assisted excitation path is discussed as responsible for the UC behavior of Yb:Er:NaT(XO4)2 compounds.

  12. Improved Charge Separation in WO3/CuWO4 Composite Photoanodes for Photoelectrochemical Water Oxidation

    Directory of Open Access Journals (Sweden)

    Danping Wang

    2016-05-01

    Full Text Available Porous tungsten oxide/copper tungstate (WO3/CuWO4 composite thin films were fabricated via a facile in situ conversion method, with a polymer templating strategy. Copper nitrate (Cu(NO32 solution with the copolymer surfactant Pluronic®F-127 (Sigma-Aldrich, St. Louis, MO, USA, generic name, poloxamer 407 was loaded onto WO3 substrates by programmed dip coating, followed by heat treatment in air at 550 °C. The Cu2+ reacted with the WO3 substrate to form the CuWO4 compound. The composite WO3/CuWO4 thin films demonstrated improved photoelectrochemical (PEC performance over WO3 and CuWO4 single phase photoanodes. The factors of light absorption and charge separation efficiency of the composite and two single phase films were investigated to understand the reasons for the PEC enhancement of WO3/CuWO4 composite thin films. The photocurrent was generated from water splitting as confirmed by hydrogen and oxygen gas evolution, and Faradic efficiency was calculated based on the amount of H2 produced. This work provides a low-cost and controllable method to prepare WO3-metal tungstate composite thin films, and also helps to deepen the understanding of charge transfer in WO3/CuWO4 heterojunction.

  13. Effects of micro-sized and nano-sized WO_3 on mass attenauation coefficients of concrete by using MCNPX code

    International Nuclear Information System (INIS)

    Tekin, H.O.; Singh, V.P.; Manici, T.

    2017-01-01

    In the present work the effect of tungsten oxide (WO_3) nanoparticles on mass attenauation coefficients of concrete has been investigated by using MCNPX (version 2.4.0). The validation of generated MCNPX simulation geometry has been provided by comparing the results with standard XCOM data for mass attenuation coefficients of concrete. A very good agreement between XCOM and MCNPX have been obtained. The validated geometry has been used for definition of nano-WO_3 and micro-WO_3 into concrete sample. The mass attenuation coefficients of pure concrete and WO_3 added concrete with micro-sized and nano-sized have been compared. It was observed that shielding properties of concrete doped with WO_3 increased. The results of mass attenauation coefficients also showed that the concrete doped with nano-WO_3 significanlty improve shielding properties than micro-WO_3. It can be concluded that addition of nano-sized particles can be considered as another mechanism to reduce radiation dose. - Highlights: • It was found that size of the WO_3 affected the mass attenuation coefficients of concrete in all photon energies.

  14. Preparation of three dimensional graphene foam–WO3 nanocomposite with enhanced visible light photocatalytic activity

    International Nuclear Information System (INIS)

    Azimirad, R.; Safa, S.

    2015-01-01

    Three dimensional graphene foam (3D GF) was synthesized by chemical vapor deposition (CVD) on a nickel foam skeleton. After dissolving the nickel foam, the obtaining 3D GF was used as a highly porous conductive substrate for nucleation and growth of WO 3 particles. Scanning electron microscopy (SEM) and Raman spectroscopy was employed to ensure the quality of the prepared GFs and to judge about the 3D GF–WO 3 chemical structure. The WO 3 characteristic Raman peaks centered at 726, and 809 cm −1 are slightly broadened and displaced to lower wavelength in the 3D GF–WO 3 nanocomposite, as compared to the corresponding peaks of the bare tungsten oxide. This phenomenon confirms the formation of W–C and W–O–C bonds in composite material which is important for faster transferring the photoexcited electrons to graphene 3D network as an exceptional electron acceptor. The 3D GF−WO 3 composite material was applied in photocatalytic degradation of Rhodamine B dye. It was observed that the annealed samples show an excellent photocatalytic performance relative to the as-prepared 3D GF−WO 3 samples and bare WO 3 , which is ascribed to the lower electron/hole recombination through the formation of W–C and W–O–C bonds. - Highlights: • 3D GF synthesized by CVD on a nickel foam as a highly porous conductive substrate. • WO 3 nanoparticles coated on 3D GF by dip-coating. • 3D GF−WO 3 shows an excellent photocatalytic degradation of Rhodamine B dye. • Better photocatalytic properties assigned to the formation of W–C and W–O–C bonds

  15. Nanospherical composite of WO{sub 3} wrapped NaTaO{sub 3}: Improved photodegradation of tetracycline under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Qu, Lingnan; Lang, Junyu; Wang, Shuwei; Chai, Zhanli; Su, Yiguo; Wang, Xiaojing, E-mail: wang_xiao_jing@hotmail.com

    2016-12-01

    Graphical abstract: - Highlights: • A novel ternary NaTaO{sub 3}@WO{sub 3} photocatalyst was successfully fabricated. • NaTaO{sub 3}@WO{sub 3} composites exhibited spherical assemblies with fine WO{sub 3} nanosheets wrapped on the cube NaTaO{sub 3} nanoparticles. • NaTaO{sub 3}@WO{sub 3} showed the enhanced photocatalytic performance in the tetracycline hydrochloride degradation under visible light irradiation. • An adsorption−degradation photocatalytic mechanism promoted through a Z-type heterojunction was proposed. - Abstract: In this paper, WO{sub 3}-wrapped NaTaO{sub 3} nanospheres photocatalysts with different W/Ta molar ratios were successfully prepared via a facile hydrothermal method. The samples were characterized by X-ray diffraction, transmission and scan electron microscopy, X-ray photoelectron spectroscopy, FT-IR spectrum, UV−vis diffuse reflectance spectroscopy, and Barrett−Emmett−Teller technique. The photocatalytic activities for degrading tetracycline hydrochloride under visible light irradiation were examined. The results indicated that the as-prepared NaTaO{sub 3}@WO{sub 3} photocatalysts showed the obvious enhancement in the tetracycline hydrochloride degradation ratio, compared with the pure NaTaO{sub 3} and WO{sub 3} under visible light irradiation. The optimum percentage of NaTaO{sub 3}@WO{sub 3} composites with a 60.88% degradation rate was W:Ta = 0.3:1 in mole, which was mainly attributed to the effective separation of the photo-generated electron and hole as well as the expanding of the absorption edge to the visible region due to the spherical heterojunction by wrapping WO{sub 3} on the surface of NaTaO{sub 3}. The radicals trapping experiments demonstrated that there were multiple active species during the degrading process of TC. The possible mechanism of tetracycline hydrochloride degradation by NaTaO{sub 3}@WO{sub 3} composite was also proposed.

  16. Microwave assisted hydrothermal synthesis of Ag/AgCl/WO3 photocatalyst and its photocatalytic activity under simulated solar light

    International Nuclear Information System (INIS)

    Adhikari, Rajesh; Gyawali, Gobinda; Sekino, Tohru; Wohn Lee, Soo

    2013-01-01

    Simulated solar light responsive Ag/AgCl/WO 3 composite photocatalyst was synthesized by microwave assisted hydrothermal process. The synthesized powders were characterized by X-Ray Diffraction (XRD) spectroscopy, X-Ray Photoelectron Spectroscopy (XPS), Transmission Electron Microscopy (TEM), Diffuse Reflectance Spectroscopy (UV–Vis DRS), and BET surface area analyzer to investigate the crystal structure, morphology, chemical composition, optical properties and surface area of the composite photocatalyst. This photocatalyst exhibited higher photocatalytic activity for the degradation of rhodamine B under simulated solar light irradiation. Dye degradation efficiency of composite photocatalyst was found to be increased significantly as compared to that of the commercial WO 3 nanopowder. Increase in photocatalytic activity of the photocatalyst was explained on the basis of surface plasmon resonance (SPR) effect caused by the silver nanoparticles present in the composite photocatalyst. Highlights: ► Successful synthesis of Ag/AgCl/WO 3 nanocomposite. ► Photocatalytic experiment was performed under simulated solar light. ► Nanocomposite photocatalyst was very active as compared to WO 3 commercial powder. ► SPR effect due to Ag nanoparticles enhanced the photocatalytic activity.

  17. CTAB-Assisted Hydrothermal Synthesis of WO3 Hierarchical Porous Structures and Investigation of Their Sensing Properties

    Directory of Open Access Journals (Sweden)

    Dan Meng

    2015-01-01

    Full Text Available WO3 hierarchical porous structures were successfully synthesized via cetyltrimethylammonium bromide- (CTAB- assisted hydrothermal method. The structure and morphology were investigated using scanning electron microscope, X-ray diffractometer, transmission electron microscopy, X-ray photoelectron spectra, Brunauer-Emmett-Teller nitrogen adsorption-desorption, and thermogravimetry and differential thermal analysis. The result demonstrated that WO3 hierarchical porous structures with an orthorhombic structure were constructed by a number of nanoparticles about 50–100 nm in diameters. The H2 gas sensing measurements showed that well-defined WO3 hierarchical porous structures with a large specific surface area exhibited the higher sensitivity compared with products without CTAB at all operating temperatures. Moreover, the reversible and fast response to H2 gas and good selectivity were obtained. The results indicated that the WO3 hierarchical porous structures are promising materials for gas sensors.

  18. In-situ transmission electron microscopy imaging of formation and evolution of LixWO3 during lithiation of WO3 nanowires

    International Nuclear Information System (INIS)

    Qi, Kuo; Li, Xiaomin; Sun, Muhua; Huang, Qianming; Wei, Jiake; Xu, Zhi; Wang, Wenlong; Bai, Xuedong; Wang, Enge

    2016-01-01

    The phase transition from monoclinic WO 3 to cubic Li x WO 3 during lithiation of WO 3 is one of the key features for tungsten oxide as the most used electrochromic material. Conventionally, the lithium intercalation of WO 3 has been studied by building generic layered electrochromic device combining with structural characterization and electrochemistry measurement at macro scale. In-situ transmission electron microscopy (in-situ TEM) has been proposed as a method for revealing the detailed mechanism of structural, physical, and chemical properties. Here, we use in-situ TEM method to investigate the formation and evolution of Li x WO 3 in real-time during the electrochemical lithiation of WO 3 nanowires. The dynamic lithiation process is recorded by TEM imaging, diffraction, and electron energy loss spectroscopy. The WO 3 -Li x WO 3 phase boundary of reaction front has been observed at high resolution. The timeliness of crystallinity of Li x WO 3 and the intercalation channels for Li ions are also identified. Moreover, the co-existence of both polycrystalline Li-poor area and amorphous Li-rich phases of Li x WO 3 was found. Our results provide an insight into the basic lithiation process of WO 3 , which is significantly important for understanding the electrochromic mechanism of tungsten oxide.

  19. Light-Driven Au-WO3@C Janus Micromotors for Rapid Photodegradation of Dye Pollutants.

    Science.gov (United States)

    Zhang, Qilu; Dong, Renfeng; Wu, Yefei; Gao, Wei; He, Zihan; Ren, Biye

    2017-02-08

    A novel light-driven Au-WO 3 @C Janus micromotor based on colloidal carbon WO 3 nanoparticle composite spheres (WO 3 @C) prepared by one-step hydrothermal treatment is described. The Janus micromotors can move in aqueous media at a speed of 16 μm/s under 40 mW/cm 2 UV light due to diffusiophoretic effects. The propulsion of such Au-WO 3 @C Janus micromotors (diameter ∼ 1.0 μm) can be generated by UV light in pure water without any external chemical fuels and readily modulated by light intensity. After depositing a paramagnetic Ni layer between the Au layer and WO 3 , the motion direction of the micromotor can be precisely controlled by an external magnetic field. Such magnetic micromotors not only facilitate recycling of motors but also promise more possibility of practical applications in the future. Moreover, the Au-WO 3 @C Janus micromotors show high sensitivity toward extremely low concentrations of sodium-2,6-dichloroindophenol (DCIP) and Rhodamine B (RhB). The moving speed of motors can be significantly accelerated to 26 and 29 μm/s in 5 × 10 -4 wt % DCIP and 5 × 10 -7 wt % RhB aqueous solutions, respectively, due to the enhanced diffusiophoretic effect, which results from the rapid photocatalytic degradation of DCIP and RhB by WO 3 . This photocatalytic acceleration of the Au-WO 3 @C Janus micromotors confirms the self-diffusiophoretic mechanism and opens an opportunity to tune the motility of the motors. This work also offers the light-driven micromotors a considerable potential for detection and rapid photodegradation of dye pollutants in water.

  20. Europium(III) chelate-dyed nanoparticles as donors in a homogeneous proximity-based immunoassay for estradiol

    International Nuclear Information System (INIS)

    Kokko, Leena; Sandberg, Kaisa; Loevgren, Timo; Soukka, Tero

    2004-01-01

    Nanoparticles containing thousands of fluorescent europium(III) chelates have a very high specific activity compared to traditional lanthanide chelate labels. It can be assumed that if these particles are used in a homogeneous assay as donors, multiple chelates can excite a single acceptor in turns and the energy transfer to the acceptor is increased. The principle was employed in an immunoassay using luminescent resonance energy transfer from a long lifetime europium(III) chelate-dyed nanoparticle to a short lifetime, near-infrared fluorescent molecule. Due to energy transfer fluorescence lifetime of the sensitised emission was prolonged and fluorescence could be measured using a time-resolved detection. A competitive homogeneous immunoassay for estradiol was created using 92 nm europium(III) chelate-dyed nanoparticle coated with 17β-estradiol specific recombinant antibody Fab fragments as a donor and estradiol conjugated with near-infrared dye AlexaFluor 680 as an acceptor. The density of Fab fragments on the surface of the particle influenced the sensitivity of the immunoassay. The optimal Fab density was reached when the entire surface of the particle participated in the energy transfer, but the areas where the energy was transferred to a single acceptor, did not overlap. We were able to detect estradiol concentrations down to 70 pmol l -1 (3xSD of a standard containing 0 nmol l -1 of E2) using a 96-well platform. In this study we demonstrated that nanoparticles containing lanthanide chelates could be used as efficient donors in homogeneous assays

  1. Polyelectrolyte-based electrochemiluminescence enhancement for Ru(bpy){sub 3}{sup 2+} loaded by SiO{sub 2} nanoparticle carrier and its high sensitive immunoassay

    Energy Technology Data Exchange (ETDEWEB)

    Ge, Zhi-Li; Song, Tian-Mei; Chen, Zhe [College of Pharmaceutical Science, Soochow University, Suzhou 215123 (China); Guo, Wu-Run [College of Pharmaceutical Science, Soochow University, Suzhou 215123 (China); College of Chemistry and Chemical Engineering, China West Normal University, Nanchong 637002 (China); Xie, Hong-Ping, E-mail: hpxie@suda.edu.cn [College of Pharmaceutical Science, Soochow University, Suzhou 215123 (China); Xie, Lian, E-mail: xielian@suda.edu.cn [College of Pharmaceutical Science, Soochow University, Suzhou 215123 (China)

    2015-03-03

    Highlights: • Preparation of strong ECL nanoparticles PAA–Ru@SiO{sub 2}/[PAA⋯Ru&Nafion⋯Ru]. • Ion-pair macromolecule PAA–Ru formed to greatly increase the doping amount. • PAA&Nafion membrane increased the amount of ion-exchanged Ru(bpy){sub 3}{sup 2+}. • PAA&Nafion membrane enhanced the ability of electron transfer. • Realized antibody labeling and established a high-sensitive immunoassay. - Abstract: In this paper the strong electrochemiluminescence (ECL) nanoparticles have been prepared based on the anionic polyelectrolyte sodium polyacrylate (PAA)-ECL enhancement for Ru(bpy){sub 3}{sup 2+}, which were loaded by the carrier of SiO{sub 2} nanoparticle. There were two kinds of Ru(bpy){sub 3}{sup 2+} for the as-prepared nanoparticles, the doped one and the exchanged one. The former was loaded inside the ECL nanoparticles by doping, in a form of ion-pair macromolecules PAA–Ru(bpy){sub 3}{sup 2+}. The corresponding ECL was enhanced about 2 times owing to the doping increase of Ru(bpy){sub 3}{sup 2+}. The latter was loaded on the PAA-doped Nafion membrane by ion exchange. The corresponding ECL was enhanced about 3 times owing to the ion-exchanging increase of Ru(bpy){sub 3}{sup 2+}. At the same time, ECL intensity of the doped-inside Ru(bpy){sub 3}{sup 2+} was further enhanced 13 times because polyelectrolyte PAA in the doped membrane could obviously enhance electron transfer between the doped Ru(bpy){sub 3}{sup 2+} and the working electrode. Furthermore, based on hydrophobic regions of the doped membrane antibody labeling could be easily realized by the as-prepared nanoparticles and then a high sensitive ECL immunoassay for HBsAg was developed. The linear range was between 1.0 and 100 pg mL{sup −1} (R{sup 2} = 0.9912). The detection limit could be as low as 0.11 pg mL{sup −1} (signal-to-noise ratio = 3)

  2. Microwave mediated synthesis of nanostructured Co -WO_3 and CoWO_4 for supercapacitor applications

    International Nuclear Information System (INIS)

    Dhilip Kumar, R.; Karuppuchamy, S.

    2016-01-01

    Co-WO_3 and CoWO_4 nanopowders have been successfully obtained from microwave mediated process. The characterization of the prepared nanopowders was carried out by X-ray diffraction (XRD), scanning electron microscopy and Energy dispersive X-ray spectroscopy techniques. The XRD pattern confirms the formation of orthorhombic and monoclinic phase of the as-synthesized and calcined samples, respectively. Scanning electron microscopic examination of the resultant powders reveals the formation of nanoporous morphology. The electrochemical performance of the Co-WO_3 and CoWO_4 coated electrodes was also investigated. The maximum specific capacitance of 45 F/g was achieved for the Co-WO_3 nanopowder. - Highlights: • Novel nano-sized Co-WO_3 and CoWO_4 materials have been prepared. • A new and simple solution growth technique was developed. • Co-WO_3 is a promising material for supercapacitor applications.

  3. A Novel Colorimetric Immunoassay Utilizing the Peroxidase Mimicking Activity of Magnetic Nanoparticles

    Directory of Open Access Journals (Sweden)

    Hyun Gyu Park

    2013-05-01

    Full Text Available A simple colorimetric immunoassay system, based on the peroxidase mimicking activity of Fe3O4 magnetic nanoparticles (MNPs, has been developed to detect clinically important antigenic molecules. MNPs with ca. 10 nm in diameter were synthesized and conjugated with specific antibodies against target molecules, such as rotaviruses and breast cancer cells. Conjugation of the MNPs with antibodies (MNP-Abs enabled specific recognition of the corresponding target antigenic molecules through the generation of color signals arising from the colorimetric reaction between the selected peroxidase substrate, 3,3',5,5'-tetramethylbenzidine (TMB and H2O2. Based on the MNP-promoted colorimetric reaction, the target molecules were detected and quantified by measuring absorbance intensities corresponding to the oxidized form of TMB. Owing to the higher stabilities and economic feasibilities of MNPs as compared to horseradish peroxidase (HRP, the new colorimetric system employing MNP-Abs has the potential of serving as a potent immunoassay that should substitute for conventional HRP-based immunoassays. The strategy employed to develop the new methodology has the potential of being extended to the construction of simple diagnostic systems for a variety of biomolecules related to human cancers and infectious diseases, particularly in the realm of point-of-care applications.

  4. Ag loaded WO_3 nanoplates for efficient photocatalytic degradation of sulfanilamide and their bactericidal effect under visible light irradiation

    International Nuclear Information System (INIS)

    Zhu, Wenyu; Liu, Jincheng; Yu, Shuyan; Zhou, Yan; Yan, Xiaoli

    2016-01-01

    Highlights: • WO_3/Ag heterogeneous composites were fabricated with simply photo-reduction method. • Property changes due to Ag loading were systematically studied. • WO_3/Ag composites efficiently degraded sulfanilamide under visible light irradiation. • WO_3/Ag composites exhibited bactericidal effectS under visible light irradiation. - Abstract: Sulfonamides (SAs) are extensively used antibiotics and their residues in the water bodies propose potential threat to the public. In this study, degradation efficiency of sulfanilamide (SAM), which is the precursor of SAs, using WO_3 nanoplates and their Ag heterogeneous as photocatalysts was investigated. WO_3 nanoplates with uniform size were synthesized by a facile one step hydrothermal method. Different amount of Ag nanoparticles (Ag NPs) were loaded onto WO_3 nanoplates using a photo-reduction method to generate WO_3/Ag composites. The physio-chemical properties of synthesized nanomaterials were systematically characterized. Photodegradation of SAM by WO_3 and WO_3/Ag composites was conducted under visible light irradiation. The results show that WO_3/Ag composites performed much better than pure WO_3 where the highest removal rate was 96.2% in 5 h. Ag as excellent antibacterial agent also endows certain antibacterial efficiency to WO_3, and 100% removal efficiency against Escherichia Coli and Bacillus subtilis could be achieved in 2 h under visible light irradiation for all three WO_3/Ag composites synthesized. The improved performance in terms of SAM degradation and antibacterial activity of WO_3/Ag can be attributed to the improved electron-hole pair separation rate where Ag NPs act as effective electron trapper during the photocatalytic process.

  5. Quantum dots as mediators in gas sensing: A case study of CdS sensitized WO{sub 3} sensing composites

    Energy Technology Data Exchange (ETDEWEB)

    Concina, Isabella, E-mail: concina@sensor.ing.unibs.it [CNR-INO SENSOR Laboratory, via Branze, 45, 25131 Brescia (Italy); SENSOR, Department of Information Engineering, Brescia University, via Valotti, 9, 25133 Brescia (Italy); Comini, Elisabetta [CNR-INO SENSOR Laboratory, via Branze, 45, 25131 Brescia (Italy); SENSOR, Department of Information Engineering, Brescia University, via Valotti, 9, 25133 Brescia (Italy); Kaciulis, Saulius [CNR-ISMN, Institute for the Study of Nanostructured Materials, Via dei Taurini, 19, 00185 Roma (Italy); Sberveglieri, Giorgio [CNR-INO SENSOR Laboratory, via Branze, 45, 25131 Brescia (Italy); SENSOR, Department of Information Engineering, Brescia University, via Valotti, 9, 25133 Brescia (Italy)

    2014-01-30

    In this study the proof of principle of the use of naked semiconductor directly generated on metal oxide surface as mediators in gas sensing is provided. Successive ionic layer absorption and reaction (SILAR) technique has been applied to sensitize a WO{sub 3} thin film with CdS quantum dots. Response to gases of bare WO{sub 3} is deeply modified: quantum dots dramatically increase the metal oxide conductance, otherwise rather poor, and modify the capability of detecting environmental pollutants, such as CO and NO{sub 2}. A modified sensing mechanism is proposed to rationalize the mediation exerted by the semiconducting active layer on the interaction between gaseous species and WO{sub 3} surface.

  6. An ultrasensitive chemiluminescence immunoassay of chloramphenicol based on gold nanoparticles and magnetic beads.

    Science.gov (United States)

    Tao, Xiaoqi; Jiang, Haiyang; Yu, Xuezhi; Zhu, Jinghui; Wang, Xia; Wang, Zhanhui; Niu, Lanlan; Wu, Xiaoping; Shen, Jianzhong

    2013-05-01

    A competitive, direct, chemiluminescent immunoassay based on a magnetic beads (MBs) separation and gold nanoparticles (AuNPs) labelling technique to detect chloramphenicol (CAP) has been developed. Horseradish peroxidase (HRP)-labelled anti-CAP monoclonal antibody conjugated with AuNPs and antigen-immobilized MBs were prepared. After optimization parameters of immunocomplex MBs, the IC50 values of chemiluminescence magnetic nanoparticles immunoassay (CL-MBs-nano-immunoassay) were 0.017 µg L(-1) for extract method I and 0.17 µg L(-1) for extract method II. The immunoassay with two extract methods was applied to detect CAP in milk. Comparison of these two extract methods showed that extract method I was advantageous in better sensitivity, in which the sensitivity was 10 times compared to that of extract method II, while extract method II was superior in simple operation, suitable for high throughout screen. The recoveries were 86.7-98.0% (extract method I) and 80.0-103.0% (extract method II), and the coefficients of variation (CVs) were all recovery with both extract methods and high correlation with traditional ELISA kit in milk system confirmed that the immunomagnetic assay based on AuNPs exhibited promising potential in rapid field screening for trace CAP analysis. Copyright © 2013 John Wiley & Sons, Ltd.

  7. In situ growth of metal particles on 3D urchin-like WO3 nanostructures.

    Science.gov (United States)

    Xi, Guangcheng; Ye, Jinhua; Ma, Qiang; Su, Ning; Bai, Hua; Wang, Chao

    2012-04-18

    Metal/semiconductor hybrid materials of various sizes and morphologies have many applications in areas such as catalysis and sensing. Various organic agents are necessary to stabilize metal nanoparticles during synthesis, which leads to a layer of organic compounds present at the interfaces between the metal particles and the semiconductor supports. Generally, high-temperature oxidative treatment is used to remove the organics, which can extensively change the size and morphology of the particles, in turn altering their activity. Here we report a facile method for direct growth of noble-metal particles on WO(3) through an in situ redox reaction between weakly reductive WO(2.72) and oxidative metal salts in aqueous solution. This synthetic strategy has the advantages that it takes place in one step and requires no foreign reducing agents, stabilizing agents, or pretreatment of the precursors, making it a practical method for the controlled synthesis of metal/semiconductor hybrid nanomaterials. This synthetic method may open up a new way to develop metal-nanoparticle-loaded semiconductor composites. © 2012 American Chemical Society

  8. Nanoparticle-based sandwich electrochemical immunoassay for carbohydrate antigen 125 with signal enhancement using enzyme-coated nanometer-sized enzyme-doped silica beads.

    Science.gov (United States)

    Tang, Dianping; Su, Biling; Tang, Juan; Ren, Jingjing; Chen, Guonan

    2010-02-15

    A novel nanoparticle-based electrochemical immunoassay of carbohydrate antigen 125 (CA125) as a model was designed to couple with a microfluidic strategy using anti-CA125-functionalized magnetic beads as immunosensing probes. To construct the immunoassay, thionine-horseradish peroxidase conjugation (TH-HRP) was initially doped into nanosilica particles using the reverse micelle method, and then HRP-labeled anti-CA125 antibodies (HRP-anti-CA125) were bound onto the surface of the synthesized nanoparticles, which were used as recognition elements. Different from conventional nanoparticle-based electrochemical immunoassays, the recognition elements of the immunoassay simultaneously contained electron mediator and enzyme labels and simplified the electrochemical measurement process. The sandwich-type immunoassay format was used for the online formation of the immunocomplex in an incubation cell and captured in the detection cell with an external magnet. The electrochemical signals derived from the carried HRP toward the reduction of H(2)O(2) using the doped thionine as electron mediator. Under optimal conditions, the electrochemical immunoassay exhibited a wide working range from 0.1 to 450 U/mL with a detection limit of 0.1 U/mL CA125. The precision, reproducibility, and stability of the immunoassay were acceptable. The assay was evaluated for clinical serum samples, receiving in excellent accordance with results obtained from the standard enzyme-linked immunosorbent assay (ELISA) method. Concluding, the nanoparticle-based assay format provides a promising approach in clinical application and thus represents a versatile detection method.

  9. Electron spin resonance spectroscopy for immunoassay using iron oxide nanoparticles as probe.

    Science.gov (United States)

    Jiang, Jia; Tian, Sizhu; Wang, Kun; Wang, Yang; Zang, Shuang; Yu, Aimin; Zhang, Ziwei

    2018-02-01

    With the help of iron oxide nanoparticles, electron spin resonance spectroscopy (ESR) was applied to immunoassay. Iron oxide nanoparticles were used as the ESR probe in order to achieve an amplification of the signal resulting from the large amount of Fe 3+ ion enclosed in each nanoparticle. Rabbit IgG was used as antigen to test this method. Polyclonal antibody of rabbit IgG was used as antibody to detect the antigen. Iron oxide nanoparticle with a diameter of either 10 or 30 nm was labeled to the antibody, and Fe 3+ in the nanoparticle was probed for ESR signal. The sepharose beads were used as solid phase to which rabbit IgG was conjugated. The nanoparticle-labeled antibody was first added in the sample containing antigen, and the antigen-conjugated sepharose beads were then added into the sample. The nanoparticle-labeled antibody bound to the antigen on sepharose beads was separated from the sample by centrifugation and measured. We found that the detection ranges of the antigen obtained with nanoparticles of different sizes were different because the amount of antibody on nanoparticles of 10 nm was about one order of magnitude higher than that on nanoparticles of 30 nm. When 10 nm nanoparticle was used as probe, the upper limit of detection was 40.00 μg mL -1 , and the analytical sensitivity was 1.81 μg mL -1 . When 30 nm nanoparticle was used, the upper limit of detection was 3.00 μg mL -1 , and the sensitivity was 0.014 and 0.13 μg mL -1 depending on the ratio of nanoparticle to antibody. Graphical abstract Schematic diagram of procedure and ESR spectra.

  10. Ag loaded WO{sub 3} nanoplates for efficient photocatalytic degradation of sulfanilamide and their bactericidal effect under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Wenyu [School of Civil and Environmental Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Nanyang Environment and Water Research Institute (NEWRI), Nanyang Technological University, 1 Cleantech Loop, CleanTech One, Singapore 637141 (Singapore); Liu, Jincheng, E-mail: JCLIU@ntu.edu.sg [School of Civil and Environmental Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Current address: Faculty of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510009 (China); Yu, Shuyan; Zhou, Yan [School of Civil and Environmental Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Nanyang Environment and Water Research Institute (NEWRI), Nanyang Technological University, 1 Cleantech Loop, CleanTech One, Singapore 637141 (Singapore); Yan, Xiaoli, E-mail: XLYAN@ntu.edu.sg [School of Civil and Environmental Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Current address: Environmental and Water Technology Centre of Innovation, Ngee Ann Polytechnic, 535 Clementi Road, Singapore 599489 (Singapore)

    2016-11-15

    Highlights: • WO{sub 3}/Ag heterogeneous composites were fabricated with simply photo-reduction method. • Property changes due to Ag loading were systematically studied. • WO{sub 3}/Ag composites efficiently degraded sulfanilamide under visible light irradiation. • WO{sub 3}/Ag composites exhibited bactericidal effectS under visible light irradiation. - Abstract: Sulfonamides (SAs) are extensively used antibiotics and their residues in the water bodies propose potential threat to the public. In this study, degradation efficiency of sulfanilamide (SAM), which is the precursor of SAs, using WO{sub 3} nanoplates and their Ag heterogeneous as photocatalysts was investigated. WO{sub 3} nanoplates with uniform size were synthesized by a facile one step hydrothermal method. Different amount of Ag nanoparticles (Ag NPs) were loaded onto WO{sub 3} nanoplates using a photo-reduction method to generate WO{sub 3}/Ag composites. The physio-chemical properties of synthesized nanomaterials were systematically characterized. Photodegradation of SAM by WO{sub 3} and WO{sub 3}/Ag composites was conducted under visible light irradiation. The results show that WO{sub 3}/Ag composites performed much better than pure WO{sub 3} where the highest removal rate was 96.2% in 5 h. Ag as excellent antibacterial agent also endows certain antibacterial efficiency to WO{sub 3}, and 100% removal efficiency against Escherichia Coli and Bacillus subtilis could be achieved in 2 h under visible light irradiation for all three WO{sub 3}/Ag composites synthesized. The improved performance in terms of SAM degradation and antibacterial activity of WO{sub 3}/Ag can be attributed to the improved electron-hole pair separation rate where Ag NPs act as effective electron trapper during the photocatalytic process.

  11. Enhanced electrochromic and energy storage performance in mesoporous WO3 film and its application in a bi-functional smart window.

    Science.gov (United States)

    Wang, Wei-Qi; Wang, Xiu-Li; Xia, Xin-Hui; Yao, Zhu-Jun; Zhong, Yu; Tu, Jiang-Ping

    2018-05-03

    Construction of multifunctional photoelectrochemical energy devices is of great importance to energy saving. In this study, we have successfully prepared a mesoporous WO3 film on FTO glass via a facile dip-coating sol-gel method; the designed mesoporous WO3 film exhibited advantages including high transparency, good adhesion and high porosity. Also, multifunctional integrated energy storage and optical modulation ability are simultaneously achieved by the mesoporous WO3 film. Impressively, the mesoporous WO3 film exhibits a noticeable electrochromic energy storage performance with a large optical modulation up to 75.6% at 633 nm, accompanied by energy storage with a specific capacity of 75.3 mA h g-1. Furthermore, a full electrochromic energy storage window assembled with the mesoporous WO3 anode and PANI nanoparticle cathode is demonstrated with large optical modulation and good long-term stability. Our research provides a new route to realize the coincident utilization of optical-electrochemical energy.

  12. PEGylated (NH4)xWO3 nanorods as efficient and stable multifunctional nanoagents for simultaneous CT imaging and photothermal therapy of tumor.

    Science.gov (United States)

    Macharia, Daniel K; Tian, Qiyun; Chen, Liang; Sun, Yingqi; Yu, Nuo; He, Chuanglong; Wang, Han; Chen, Zhigang

    2017-09-01

    The simultaneous imaging and photothermal therapy of tumors have attracted much attention, and a prerequisite is to obtain multifunctional nanomaterials. Ideally, one kind of nanoparticles with single component can be used as both imaging agent and photothermal agent. Herein, we have developed the PEGylated (NH 4 ) x WO 3 (denoted as (NH 4 ) x WO 3 -PEG) nanorods as multifunctional nanoparticles with single semiconductor component. (NH 4 ) x WO 3 -PEG nanorods with about 30nm diameter and length of several hundred nanometers have been obtained through a solvothermal synthesis-PEGylation two-step route. Under the irradiation of 980-nm laser with intensity of 0.72Wcm -2 , aqueous dispersion of (NH 4 ) x WO 3 -PEG nanorods (0.67-5.44mmol/L) displays high elevation (17.6-34.5°C) of temperature in 400s, accompanied by an excellent long-term photothermal stability. Furthermore, (NH 4 ) x WO 3 -PEG nanorods exhibit as high as 6 times X-ray attenuation ability compared to that of the clinically used iodine-based X-ray computed tomography (CT) contrast agent (Iopromide). More importantly, after PBS solution of (NH 4 ) x WO 3 -PEG nanorods is injected into the tumor of mice, the tumor can be effectively detected by CT imaging. Moreover, cancer cells in vivo can be further destroyed by the photothermal effects of (NH 4 ) x WO 3 -PEG nanorods, under the irradiation of 980-nm laser with the safe intensity of 0.72Wcm -2 for 10min. Therefore, (NH 4 ) x WO 3 -PEG nanorods can be used as a new kind of stable and efficient multifunctional nanoagent with single component for simultaneous CT imaging and photothermal therapy of tumor. Copyright © 2017. Published by Elsevier B.V.

  13. Phase diagrams of KY(WO4)2-KEr(WO4)2, KGd(WO4)2-KEr(WO4)2 systems and single crystal growth for some tungstates

    International Nuclear Information System (INIS)

    Yudanova, L.I.; Pavlyuk, A.A.; Potapova, O.G.

    1992-01-01

    Phase diagrams of the KY(WO 4 ) 2 -KEr(WO 4 ) 2 , KGd(WO 4 ) 2 -KEr(WO 4 ) 2 systems were studied by differential thermal and X-ray diffraction analyses. Continuous variety of solid solutions are in the KY(WO 4 ) 2 -KEr(WO 4 ) 2 system. They occurred just as in the area of alphaso beta-modifications. Limited areas of the solid solutions based on components were in the KGd(WO 4 ) 2 -KEr(WO 4 ) 2 system. Monocrystals of potassium-yttrium and potassium-gadolinium tungstates activated by erbium were grown using modified low-gradient Czochralski method

  14. In situ growth of Ag nanoparticles on α-Ag2WO4 under electron irradiation: probing the physical principles

    Science.gov (United States)

    San-Miguel, Miguel A.; da Silva, Edison Z.; Zannetti, Sonia M.; Cilense, Mario; Fabbro, Maria T.; Gracia, Lourdes; Andrés, Juan; Longo, Elson

    2016-06-01

    Exploiting the plasmonic behavior of Ag nanoparticles grown on α-Ag2WO4 is a widely employed strategy to produce efficient photocatalysts, ozone sensors, and bactericides. However, a description of the atomic and electronic structure of the semiconductor sites irradiated by electrons is still not available. Such a description is of great importance to understand the mechanisms underlying these physical processes and to improve the design of silver nanoparticles to enhance their activities. Motivated by this, we studied the growth of silver nanoparticles to investigate this novel class of phenomena using both transmission electron microscopy and field emission scanning electron microscopy. A theoretical framework based on density functional theory calculations (DFT), together with experimental analysis and measurements, were developed to examine the changes in the local geometrical and electronic structure of the materials. The physical principles for the formation of Ag nanoparticles on α-Ag2WO4 by electron beam irradiation are described. Quantum mechanical calculations based on DFT show that the (001) of α-Ag2WO4 displays Ag atoms with different coordination numbers. Some of them are able to diffuse out of the surface with a very low energy barrier (less than 0.1 eV), thus, initiating the growth of metallic Ag nanostructures and leaving Ag vacancies in the bulk material. These processes increase the structural disorder of α-Ag2WO4 as well as its electrical resistance as observed in the experimental measurements.

  15. Tuning the pure monoclinic phase of WO3 and WO3-Ag nanostructures for non-enzymatic glucose sensing application with theoretical insight from electronic structure simulations

    Science.gov (United States)

    Ponnusamy, Rajeswari; Gangan, Abhijeet; Chakraborty, Brahmananda; Sekhar Rout, Chandra

    2018-01-01

    Here, we report the controlled hydrothermal synthesis and tuning of the pure monoclinic phase of WO3 and WO3-Ag nanostructures. Comparative electrochemical nonenzymatic glucose sensing properties of WO3 and WO3-Ag were investigated by cyclic voltammetry and chronoamperometric tests. We observed enhanced glucose sensing performance of WO3-Ag porous spheres as compared to bare WO3 nanoslabs. The sensitivity of the pure WO3 nanoslabs is 11.1 μA μM-1 cm-2 whereas WO3-Ag porous spheres exhibit sensitivity of 23.3 μA μM-1 cm-2. The WO3-Ag porous spheres exhibited a good linear range (5-375 μM) with excellent anti-interference property. Our experimental observations are qualitatively supported by density functional theory simulations through investigation of bonding and charge transfer mechanism of glucose on WO3 and Ag doped WO3. As the binding energy of glucose is more on the Ag doped WO3 (100) surface compared to the bare WO3 (100) surface and the Ag doped WO3 (100) surface becomes more conducting due to enhancement of density of states near the Fermi level, we can infer that Ag doped WO3 exhibits a better charge transfer media compared to bare WO3 resulting in enhanced glucose sensitivity in consistency with our experimental data.

  16. In situ synthesis of CdS/CdWO4/WO3 heterojunction films with enhanced photoelectrochemical properties

    Science.gov (United States)

    Zhan, Faqi; Li, Jie; Li, Wenzhang; Yang, Yahui; Liu, Wenhua; Li, Yaomin

    2016-09-01

    CdS/CdWO4/WO3 heterojunction films on fluorine-doped tin oxide (FTO) substrates are for the first time prepared as an efficient photoanode for photoelectrochemical (PEC) hydrogen generation by an in situ conversion process. The samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), ultraviolet visible spectrometry (UV-vis) and X-ray photoelectron spectroscopy (XPS). The CdS hollow spheres (∼80 nm) sensitized WO3 plate film with a CdWO4 buffer-layer exhibits increased visible light absorption and a significantly improved photoelectrochemical performance. The photocurrent density at 0 V (vs. Ag/AgCl) of the CdS/CdWO4/WO3 anode is ∼3 times higher than that of the CdWO4/WO3 anode, and ∼9 times higher than that of pure WO3 under illumination. The highest incident-photon-to-current-efficiency (IPCE) value increased from 16% to 63% when the ternary heterojunction was formed. This study demonstrates that the synthesis of ternary composite photocatalysts by the in situ conversion process may be a promising approach to achieve high photoelectric conversion efficiency.

  17. Ultrasensitive and accelerated detection of ciguatoxin by capillary electrophoresis via on-line sandwich immunoassay with rotating magnetic field and nanoparticles signal enhancement.

    Science.gov (United States)

    Zhang, Zhaoxiang; Zhang, Chaoying; Luan, Wenxiu; Li, Xiufeng; Liu, Ying; Luo, Xiliang

    2015-08-12

    A sensitive and rapid on-line immunoassay for the determination of ciguatoxin CTX3C was developed based on a capillary mixing system, which was integrated with capillary electrophoresis (CE) separation and electrochemical (EC) detection. In the sandwich immunoassay system, anti-CTX3C-functionalized magnetic nanoparticles were used as immunosensing probes, and horseradish peroxidase (HRP) and anti-CTX3C antibody were bound onto the surface of gold nanoparticles (AuNPs) and used as recognition elements. Online formation of immunocomplex was realized in capillary inlet end with an external rotating magnetic field. Compared with classical HPLC-MS and ELISA, the assay adopting AuNPs as multienzyme carriers and online sandwich immunoassay format with rotating magnetic field exhibited higher sensitivity and shorter assay time. The linear range of the assay for CTX3C was from 0.6 to 150 ng/L with a correlation coefficient of 0.9948 (n = 2), and the detection limit (S/N = 3) was 0.09 ng/L. The developed assay showed satisfying reproducibility and stability, and it was successfully applied for the quantification of CTX3C in fish samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  18. Characterization of nanoparticles of lidocaine in w/o microemulsions using small-angle neutron scattering and dynamic light scattering

    Science.gov (United States)

    Shukla, A.; Kiselev, M. A.; Hoell, A.; Neubert, R. H. H.

    2004-08-01

    Microemulsions (MEs) are of special interest because a variety of Reactants can be introduced into the nanometer-sized aqueous domains, leading to materials with controlled size and shape [1,2]. In the past few years, significant research has been conducted in the reverse ME-mediated synthesis of organic nanoparticles [3,4]. In this study, a w/o ME medium was employed for the synthesis of lidocaine by direct precipitation in w/o microemulsion systems: water/isopropylpalmitat/Tween80/Span80. The particle size as well as the location of nanoparticles in the ME droplet were characterized by means of dynamic light scattering (DLS) and small angle neutron scattering (SANS). It is observed that lidocaine precipitated in the aqueous cores because of its insolubility in water. Hydrodynamic radius and gyration radius of microemulsion droplets were estimated as ~15 nm and ~4.50 nm from DLS and SANS respectively. Furthermore, different size parameters obtained by DLS and SANS experiments were compared

  19. Homogeneous immunoassay for human IgG using oriented hen egg IgY immobilized on gold sol nanoparticles

    International Nuclear Information System (INIS)

    Yeritsyan, H.E.; Gasparyan, V.K.

    2012-01-01

    Homogeneous immunoassays using (red) gold nanoparticles represent an attractive detection scheme because of the option of photometric readout. We have applied oriented immobilization of hen egg immunoglobulin Y (IgY) on gold nanoparticles when developing a homogeneous immunoassay for human IgG. In oriented immobilization, as opposed to random immobilization, the antigen binding capabilities of the antibodies are retained. It is shown that such immunoassay has significantly better sensitivity in comparison with methods based on conventional immobilization of affinity-purified antibodies. It is also shown that hen egg IgY is better suited than rabbit antibodies, because much more antibody can be immobilized on gold nanoparticles without any destabilization, probably because of the more acidic nature of these antibodies. In addition, hen egg IgY can be supplied in higher quantity and can be prepared more easily than IgG from rabbits. Bleeding and slaughtering of animals is not needed. The assay presented here has a wide detection range (30-500 ng. mL -1 ) and a limit of detection as low as 30 ng. mL -1 of human IgG. (author)

  20. Temperature dependent selective detection of hydrogen and acetone using Pd doped WO3/reduced graphene oxide nanocomposite

    Science.gov (United States)

    Kaur, Jasmeet; Anand, Kanica; Kohli, Nipin; Kaur, Amanpreet; Singh, Ravi Chand

    2018-06-01

    Reduced graphene oxide (RGO) and Pd doped WO3 nanocomposites were fabricated by employing electrostatic interactions between poly (diallyldimethylammonium chloride) (PDDA) modified Pd doped WO3 nanostructures and graphite oxide (GO) and studied for their gas sensing application. XRD, Raman, FTIR, FESEM-EDX, TEM, TGA, XPS and Photoluminescence techniques were used for characterization of as-synthesized samples. Gas sensing studies revealed that the sensor with optimized doping of 1.5 mol% Pd and 1 wt% GO shows temperature dependent selectivity towards hydrogen and acetone. The role of WO3, Pd and RGO has been discussed in detail for enhanced sensing performance.

  1. Alkaline phosphatase labeled SERS active sandwich immunoassay for detection of Escherichia coli

    Science.gov (United States)

    Bozkurt, Akif Goktug; Buyukgoz, Guluzar Gorkem; Soforoglu, Mehmet; Tamer, Ugur; Suludere, Zekiye; Boyaci, Ismail Hakki

    2018-04-01

    In this study, a sandwich immunoassay method utilizing enzymatic activity of alkaline phosphatase (ALP) on 5-bromo-4-chloro-3-indolyl phosphate (BCIP) for Escherichia coli (E. coli) detection was developed using surface enhanced Raman spectroscopy (SERS). For this purpose, spherical magnetic gold coated core-shell nanoparticles (MNPs-Au) and rod shape gold nanoparticles (Au-NRs) were synthesized and modified for immunomagnetic separation (IMS) of E. coli from the solution. In order to specify the developed method to ALP activity, Au-NRs were labeled with this enzyme. After successful construction of the immunoassay, BCIP substrate was added to produce the SERS-active product; 5-bromo-4-chloro-3-indole (BCI). A good linearity (R2 = 0.992) was established between the specific SERS intensity of BCI at 600 cm- 1 and logarithmic E. coli concentration in the range of 1.7 × 101-1.7 × 106 cfu mL- 1. LOD and LOQ values were also calculated and found to be 10 cfu mL- 1 and 30 cfu mL- 1, respectively.

  2. Nanoparticle-based immunosensors and immunoassays for aflatoxins

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xu; Niessner, Reinhard [Institute of Hydrochemistry and Chair of Analytical Chemistry, Technische Universität München, Marchioninistrasse 17, D-81377 München (Germany); Tang, Dianping [Key Laboratory of Analysis and Detection for Food Safety, MOE & Fujian Province, Department of Chemistry, Fuzhou University, Fuzhou 350108 (China); Knopp, Dietmar, E-mail: dietmar.knopp@ch.tum.de [Institute of Hydrochemistry and Chair of Analytical Chemistry, Technische Universität München, Marchioninistrasse 17, D-81377 München (Germany)

    2016-03-17

    Aflatoxins are naturally existing mycotoxins produced mainly by Aspergillus flavus and Aspergillus parasiticus, present in a wide range of food and feed products. Because of their extremely high toxicity and carcinogenicity, strict control of maximum residue levels of aflatoxins in foodstuff is set by many countries. In daily routine, different chromatographic methods are used almost exclusively. As supplement, in several companies enzyme immunoassay-based sample testing as primary screening is performed. Recently, nanomaterials such as noble metal nanoparticles, magnetic particles, carbon nanomaterials, quantum dots, and silica nanomaterials are increasingly utilized for aflatoxin determination to improve the sensitivity and simplify the detection. They are employed either as supports for the immobilization of biomolecules or as electroactive or optical labels for signal transduction and amplification. Several nanoparticle-based electrochemical, piezoelectric, optical, and immunodipstick assays for aflatoxins have been developed. In this review, we summarize these recent advances and illustrate novel concepts and promising applications in the field of food safety. - Highlights: • Novel concepts and promising applications of nanoparticle-based immunological methods for the determination of aflatoxins. • Inclusion of most important nanomaterials and hybrid nanostructures. • Inclusion of electrochemical, optical and mass-sensitive biosensors as well as optical and immunochromatographic assays.

  3. Time-Resolved Fluorescence Immunoassay for C-Reactive Protein Using Colloidal Semiconducting Nanoparticles

    Directory of Open Access Journals (Sweden)

    Pekka Hänninen

    2011-11-01

    Full Text Available Besides the typical short-lived fluorescence with decay times in the nanosecond range, colloidal II/VI semiconductor nanoparticles dispersed in buffer also possess a long-lived fluorescence component with decay times in the microsecond range. Here, the signal intensity of the long-lived luminescence at microsecond range is shown to increase 1,000-fold for CdTe nanoparticles in PBS buffer. This long-lived fluorescence can be conveniently employed for time-gated fluorescence detection, which allows for improved signal-to-noise ratio and thus the use of low concentrations of nanoparticles. The detection principle is demonstrated with a time-resolved fluorescence immunoassay for the detection of C-reactive protein (CRP using CdSe-ZnS nanoparticles and green light excitation.

  4. Synthesis and Characterization of Graphene Oxide-Modified Bi2WO6 and Its Use as Photocatalyst

    Directory of Open Access Journals (Sweden)

    Xiaoyue Hu

    2016-01-01

    Full Text Available A Bi2WO6 photocatalyst modified with graphene was synthesized in a two-step template-free hydrothermal process. The prepared samples were characterized to explore their properties. The photocatalytic activities of the prepared samples were investigated by degrading dye model, Rhodamine B (RhB, under visible light irradiation. This showed that the modified Bi2WO6 photocatalyst with 1.2 wt% of graphene greatly improved photocatalytic activity during the degradation of dye pollutants, compared to pure Bi2WO6. The enhancement can be interpreted as the integrated effects of ultrahigh charge carriers’ mobility and high adsorption of RhB on graphene. Additionally, effects including catalysts dosage amount, pH of RhB solution, and temperature of reactor on the photocatalytically degrading RhB were also studied and discussed.

  5. WO3 Nanofiber-Based Biomarker Detectors Enabled by Protein-Encapsulated Catalyst Self-Assembled on Polystyrene Colloid Templates.

    Science.gov (United States)

    Choi, Seon-Jin; Kim, Sang-Joon; Cho, Hee-Jin; Jang, Ji-Soo; Lin, Yi-Min; Tuller, Harry L; Rutledge, Gregory C; Kim, Il-Doo

    2016-02-17

    A novel catalyst functionalization method, based on protein-encapsulated metallic nanoparticles (NPs) and their self-assembly on polystyrene (PS) colloid templates, is used to form catalyst-loaded porous WO3 nanofibers (NFs). The metallic NPs, composed of Au, Pd, or Pt, are encapsulated within a protein cage, i.e., apoferritin, to form unagglomerated monodispersed particles with diameters of less than 5 nm. The catalytic NPs maintain their nanoscale size, even following high-temperature heat-treatment during synthesis, which is attributed to the discrete self-assembly of NPs on PS colloid templates. In addition, the PS templates generate open pores on the electrospun WO3 NFs, facilitating gas molecule transport into the sensing layers and promoting active surface reactions. As a result, the Au and Pd NP-loaded porous WO3 NFs show superior sensitivity toward hydrogen sulfide, as evidenced by responses (R(air)/R(gas)) of 11.1 and 43.5 at 350 °C, respectively. These responses represent 1.8- and 7.1-fold improvements compared to that of dense WO3 NFs (R(air)/R(gas) = 6.1). Moreover, Pt NP-loaded porous WO3 NFs exhibit high acetone sensitivity with response of 28.9. These results demonstrate a novel catalyst loading method, in which small NPs are well-dispersed within the pores of WO3 NFs, that is applicable to high sensitivity breath sensors. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. WO3 nano-ribbons: their phase transformation from tungstite (WO3·H2O) to tungsten oxide (WO3)

    DEFF Research Database (Denmark)

    Ahmadi, Majid; Sahoo, Satyaprakash; Younesi, Reza

    2014-01-01

    Tungsten oxide (WO3) nano-ribbons (NRs) were obtained by annealing tungstite (WO3·H2O) NRs. The latter was synthesized below room temperature using a simple, environmentally benign, and low cost aging treatment of precursors made by adding hydrochloric acid to diluted sodium tungstate solutions (...

  7. Rational design of Raman-labeled nanoparticles for a dual-modality, light scattering immunoassay on a polystyrene substrate.

    Science.gov (United States)

    Israelsen, Nathan D; Wooley, Donald; Hanson, Cynthia; Vargis, Elizabeth

    2016-01-01

    Surface-enhanced Raman scattering (SERS) is a powerful light scattering technique that can be used for sensitive immunoassay development and cell labeling. A major obstacle to using SERS is the complexity of fabricating SERS probes since they require nanoscale characterization and optical uniformity. The light scattering response of SERS probes may also be modulated by the substrate used for SERS analysis. A typical SERS substrate such as quartz can be expensive. Polystyrene is a cheaper substrate option but can decrease the SERS response due to interfering Raman emission peaks and high background fluorescence. The goal of this research is to develop an optimized process for fabricating Raman-labeled nanoparticles for a SERS-based immunoassay on a polystyrene substrate. We have developed a method for fabricating SERS nanoparticle probes for use in a light scattering immunoassay on a polystyrene substrate. The light scattering profile of both spherical gold nanoparticle and gold nanorod SERS probes were characterized using Raman spectroscopy and optical absorbance spectroscopy. The effects of substrate interference and autofluorescence were reduced by selecting a Raman reporter with a strong light scattering response in a spectral region where interfering substrate emission peaks are minimized. Both spherical gold nanoparticles and gold nanorods SERS probes used in the immunoassay were detected at labeling concentrations in the low pM range. This analytical sensitivity falls within the typical dynamic range for direct labeling of cell-surface biomarkers using SERS probes. SERS nanoparticle probes were fabricated to produce a strong light scattering signal despite substrate interference. The optical extinction and inelastic light scattering of these probes was detected by optical absorbance spectroscopy and Raman spectroscopy, respectively. This immunoassay demonstrates the feasibility of analyzing strongly enhanced Raman signals on polystyrene, which is an

  8. Nonlinear current-voltage characteristics of WO3-x nano-/micro-rods

    Science.gov (United States)

    Shen, Zhenguang; Peng, Zhijian; Zhao, Zengying; Fu, Xiuli

    2018-04-01

    A series of crystalline tungsten oxide nano-/micro-rods with different compositions of WO3, WO2.90, W19O55 (WO2.89) and W18O49 (WO2.72) but identical morphology feature were first prepared. Then, various nanoscaled electrical devices were fabricated from them by micro-fabrication through a focused ion beam technique. Interestingly, the devices from the oxygen-deficient WO3-x display significantly nonlinear current-voltage characteristics. The calculated nonlinear coefficients of the WO2.90, WO2.83, and WO2.72 varistors are 2.52, 3.32 and 4.91, respectively. The breakdown voltage of the WO2.90, WO2.83, and WO2.72 varistors are 1.93, 1.28 and 0.93 V, respectively. Such WO3-x nano-varistors might be promising for low-voltage electrical/electronic devices.

  9. Silver nanoparticles deposited on graphene oxide for ultrasensitive surface-enhanced Raman scattering immunoassay of cancer biomarker.

    Science.gov (United States)

    Yang, Lin; Zhen, Shu Jun; Li, Yuan Fang; Huang, Cheng Zhi

    2018-06-14

    Graphene oxide (GO) exhibits distinctive Raman scattering features for its high frequency D (disordered) and tangential modes (G-band), which are characteristically sharp at 1580 cm-1 and 1350 cm-1, respectively, but are too weak for sensitive quantitation purposes. By depositing silver nanoparticles on the surface of GO in this contribution, both D and G bands of GO become enhanced. The enzyme label of this method controls the dissolution of silver nanoparticles on the surface of GO through hydrogen peroxide which is produced by the oxidation of the enzyme substrate. With the dissolution of the silver nanoparticles a greatly decreased SERS signal of GO was obtained. This strategy involves dual signal amplification of the enzyme and nanocomposites to improve the detection sensitivity. As a proof of concept, prostate specific antigen (PSA), a biomarker for prostate cancer, is successfully detected as a target by forming a sandwich structure in immunoassay. The SERS immunoassay possesses excellent analytical performance in the range 0.5 pg mL-1 to 500 pg mL-1 with a limit of detection of 0.23 pg mL-1, making the detection of PSA serum samples from prostate cancer patients satisfactory, demonstrating that the sensitive enzyme-assisted dissolved AgNPs SERS immunoassay of PSA has potential applications in clinical diagnosis.

  10. Synthesis and purification of oxide nanoparticle dispersions by modified emulsion precipitation.

    Science.gov (United States)

    Shi, Jingyu; Verweij, Henk

    2005-06-07

    ZrO2 and Fe2O3 precursor nanoparticles are synthesized, well-dispersed in decane, via a modified emulsion precipitation (MEP) method. This method starts with preparing two thermostable water-in-oil (w/o) emulsions with nonylphenol tetra(ethylene glycol) ether (Arkopal-40) as the main surfactant, didodecyldimethylammonium bromide (DiDAB) as the cosurfactant, decane as the continuous oil phase, and either a metal salt solution or a hexamethylenetetramine (HMTA) precipitation agent solution as the dispersed water phase. After mixing of the two emulsions, individual precursor particles are formed by precipitation in the confinement of the aqueous solution droplets. Excess water is removed by azeotropic distillation, and steric stabilization of the particles in the remaining oil medium is achieved with poly(octadecyl methacrylate) (PODMA), initially present dissolved in the oil phase. A purification process is conducted to remove the precipitation reaction byproduct and excess surfactants from the nanoparticle dispersions. Transmission electron microscopy (TEM) characterization shows that the ZrO2 and Fe2O3 precursor nanoparticles are both non-agglomerated, spherical, and have a narrow particle size distribution, centered at 4 nm in diameter. The precipitation from the dispersion of byproduct NH4Cl after water removal, and insoluble surfactant DiDAB after dilution with pure decane, is confirmed by X-ray diffraction (XRD). NMR results show that most of the oil-soluble surfactant Arkopal-40 can be removed from the dispersion by a 3x repeated dead-end pressure filtration process. It is shown that, after purification, the nanoparticle dispersions can be used for the preparation of homogeneous nanostructured coatings. The purification procedure as discussed provides guidelines for up-scaling the process and reuse of emulsifiers.

  11. Hybrid bulk heterojunction solar cells based on poly(3-hexylthiophene) and ZnO nanoparticles modified by side-chain functional polythiophenes

    International Nuclear Information System (INIS)

    Li, Fan; Du, Yanhui; Chen, Yiwang

    2012-01-01

    We report the investigation of the hybrid bulk heterojunction solar cells based on the blend of poly(3-hexylthiophene) (P3HT) and ZnO nanoparticles modified by side-chain thiol functional poly(3-thiophenehexanethiol) (P3HT-SH). Grafting of P3HT-SH onto ZnO nanoparticles can promote the dispersion of ZnO nanoparticles within P3HT matrix and facilitate electron injection process into ZnO nanoparticles, resulting in a more efficient photoinduced charge transfer than that in simple physical mixture of P3HT and non-modified ZnO nanoparticles (P3HT/ZnO). Furthermore, the performance of hybrid photovoltaic device based on P3HT/P3HT-SH-modified ZnO blend exhibits an improved device efficiency compared with P3HT/ZnO even before thermal treatment. After being annealed at 80 °C, the P3HT/P3HT-SH-modified ZnO device shows the power conversion efficiency as high as 0.68%, with the short-circuit current density of 1.89 mA/cm 2 , the open-circuit voltage of 0.599 V and a fill factor of 60.5% under AM 1.5 G illumination with 100 mW/cm 2 light intensity. - Highlights: ► Hybrid solar cells based on poly(3-hexylthiophene) and modified ZnO nanoparticles ► ZnO nanoparticles modified by side-chain functional polythiophenes ► Uniform dispersion and intimate contact between polymers and nanoparticles ► Efficient charge transfer leading to the improvement of device efficiency

  12. Label-Free Electrochemical Immunoassay for C-Reactive Protein

    Directory of Open Access Journals (Sweden)

    Madasamy Thangamuthu

    2018-03-01

    Full Text Available C-reactive protein (CRP is one of the most expressed proteins in blood during acute phase inflammation, and its minute level increase has also been recognized for the clinical diagnosis of cardio vascular diseases. Unfortunately, the available commercial immunoassays are labour intensive, require large sample volumes, and have practical limitations, such as low stability and high production costs. Hence, we have developed a simple, cost effective, and label-free electrochemical immunoassay for the measurement of CRP in a drop of serum sample using an immunosensor strip made up of a screen printed carbon electrode (SPE modified with anti-CRP functionalized gold nanoparticles (AuNPs. The measurement relies on the decrease of the oxidation current of the redox indicator Fe3+/Fe2+, resulting from the immunoreaction between CRP and anti-CRP. Under optimal conditions, the present immunoassay measures CRP in a linear range from 0.4–200 nM (0.047–23.6 µg mL−1, with a detection limit of 0.15 nM (17 ng mL−1, S/N = 3 and sensitivity of 90.7 nA nM−1, in addition to a good reproducibility and storage stability. The analytical applicability of the presented immunoassay is verified by CRP measurements in human blood serum samples. This work provides the basis for a low-priced, safe, and easy-to-use point-of-care immunosensor assay to measure CRP at clinically relevant concentrations.

  13. Structural, vibrational, and gasochromic properties of porous WO sub 3 films templated with a sol-gel organic-inorganic hybrid

    CERN Document Server

    Opara-Krasovec, U; Orel, B; Grdadolnik, J; Drazic, G

    2002-01-01

    The structure and the gasochromic properties of sol-gel-derived WO sub 3 films with a monoclinic structure (m-WO sub 3) were studied by focusing attention on the size of the monoclinic grains. The size of the m-WO sub 3 grains is modified by the addition of an organic-inorganic hybrid to the initial peroxopolytungstic acid (W-PTA) sols which are based on chemically bonded poly-(propylene glycol) to triethoxysilane end-capping groups (ICS-PPG). The results obtained with scanning electron microscopy (SEM) and transmission electron microscopy (TEM) show that the heat treatment (500 sup o C) of WO sub 3 /ICS- IPG (0.5, 1, 2, 5, and 10 mol%) composite films results in a change of their morphology, and nanodimensional pores are formed between the grains. High-resolution TEM (HRTEM) analysis revealed the presence of an amorphous phase on the outside of the m-WO sub 3 grains, whereas energy-dispersive x-ray spectra (EDXS) showed that this amorphous phase contained W and Si. Impregnation of the WO sub 3 /ICS-PPG film ...

  14. Magnetic Bead and Fluorescent Silica Nanoparticles Based Optical Immunodetection of Staphylococcal Enterotoxin B (SEB in Bottled Water

    Directory of Open Access Journals (Sweden)

    Shiva K. RASTOGI

    2009-10-01

    Full Text Available Staphylococcal enterotoxins (SEs are a major cause of food-borne diseases, most commonly SEs assayed immunologically with ELISA. An immunoassay based on fluorescein dye doped silica dioxide nanoparticles (F-SiNPs and magnetic bead (MB is described here for the detection of staphylococcal enterotoxin B (SEB. F-SiNPs have unique optical properties which make them attractive for biosensing. The water-in-oil (W/O reverse microemulsion method was used for the synthesis of F-SiNPs (~ 95 nm of diameter. The F-SiNPs were characterized using SEM, TEM and FTIR spectroscopy. The detection of SEB is preformed in PBS buffer, and bottled drinking water using sandwich immunoassay format. Target analytes were captured using MBs modified with the antigen-specific “capture” antibody, and detected using F-SiNP labeled secondary antigen-specific antibody. We report a limit of detection down to 1 ng/mL SEB spiked sample in less than 2 hr assay time using fluorocount method. This study demonstrates the bio warfare agent SEB capture by magnetic beads and detection using F-SiNPs.

  15. Synthesis, Characterization, and Gas Sensing Applications of WO3 Nanobricks

    Science.gov (United States)

    Xiao, Jingkun; Song, Chengwen; Dong, Wei; Li, Chen; Yin, Yanyan; Zhang, Xiaoni; Song, Mingyan

    2015-08-01

    WO3 nanobricks are fabricated by a simple hydrothermal method. Morphology and structure of the WO3 nanobricks are characterized by scanning electron microscopy and x-ray diffraction. Gas sensing properties of the as-prepared WO3 sensor are systematically investigated by a static gas sensing system. The results show that the WO3 nanobricks with defect corners demonstrate good crystallinity, and the mean edge length and wall thickness are 1-1.5 and 400 nm, respectively. The WO3 sensor achieves its maximum sensitivity to 100 ppm ethanol at the optimal operating temperature of 300 °C. Ultra-fast response time (2-3 s) and fast recovery time (4-11 s) of the WO3 sensor toward 100 ppm ethanol are also observed at this optimal operating temperature. Moreover, the WO3 sensor exhibits high selectivity to other gases such as methanol, benzene, hexane, and dichloromethane, indicating its excellent potential application as a gas sensor for ethanol detection.

  16. Synthesis and characterization of oleic acid surface modified magnetic iron oxide nanoparticles by using biocompatible w/o microemulsion for heavy metal removal

    Science.gov (United States)

    Rose, Laili Che; Suhaimi, Hamdan; Mamat, Mazidah; Lik, Thang Zhe

    2017-09-01

    Oleic acid modified magnetic iron oxide nanoparticles (OA-MIONs) was prepared for removal of Cu2+ ion from aqueous solution. OA-MIONs was prepared by W/O microemulsion template which composed of mixed non-ionic surfactants and 1-hexanol as emulsifier. The effect of weight ratio of the constituent of microemulsion template on the physical and chemical properties of OA-MIONs was studied by characterization using Fourier transform infrared (FT-IR), scanning electron microscopy (SEM) and X-ray powder diffraction (XRD) analysis. FT-IR spectra showed that all templates shared similar chemical structure with slight difference in the peak intensity. Scanning electron micrograph illustrated that the OA-MIONs synthesized via template with the lowest weight ratio of emulsifier to heptane had a more regular spherical shape and was well-distributed. XRD had confirmed that the identity of synthesized OA-MIONs was Fe3O4. Based on the characterization result, the template with lowest weight ratio of emulsifier to heptane was chosen for the heavy metal adsorption study. The adsorption capacity OA-MIONs as a function of pH, contact time and adsorbent dosage were studied. The adsorption process reached equilibrium for 90 minutes and successfully adsorbed 43% of Cu2+ ion from aqueous solution. The adsorption behavior was well described by Langmuir isotherm. The maximum adsorption capacity was determined and found to be 555.56 mg/g. The value of Langmuir equilibrium parameter, RL was found between 0 and 1, suggested that a favorable monolayer adsorption process had taken out.

  17. Monodisperse magnetite (Fe_3O_4) nanoparticles modified with water soluble polymers for the diagnosis of breast cancer by MRI method

    International Nuclear Information System (INIS)

    Rezayan, Ali Hossein; Mousavi, Majid; Kheirjou, Somayyeh; Amoabediny, Ghasem; Ardestani, Mehdi Shafiee; Mohammadnejad, Javad

    2016-01-01

    In this study, magnetic nanoparticles (MNPs) were synthesized via co-precipitation method. To enhance the biocompatibility and colloidal stability of the synthesized nanoparticles, they were modified with carboxyl functionalized PEG via dopamine (DPA) linker. Both modified and unmodified Fe_3O_4 nanoparticles exhibited super paramagnetic behavior (particle size below 20 nm). The saturation magnetization (Ms) of PEGdiacid-modified Fe_3O_4 was 45 emu/g, which was less than the unmodified Fe_3O_4 nanoparticles (70 emu/g). This difference indicated that PEGdiacid polymer was immobilized on the surface of Fe_3O_4 nanoparticles successfully. To evaluate the efficiency of the resulting nanoparticles as contrast agents for magnetic resonance imaging (MRI), different concentration of MNPs and different value of echo time TE were investigated. The results showed that by increasing the concentration of the nanoparticles, transverse relaxation time (T_2) decreased, which subsequently resulted in MR signal enhancement. T_2-weighted MR images of the different concentration of MNPs in different value of echo time TE indicated that MR signal intensity increased with increase in TE value up to 66 and then remained constant. The cytotoxicity effect of the modified and unmodified nanoparticles was evaluated in three different concentrations (12, 60 and 312 mg l"−"1) on MDA-MB-231 cancer cells for 24 and 48 h. In both tested time (24 and 48 h) for all three samples, the modified nanoparticles had long life time than unmodified nanoparticles. Cellular uptake of modified MNPs was 80% and reduced to 9% by the unmodified MNPs. - Highlights: • Magnetic nanoparticles (MNPs) were synthesized via co-precipitation method. • MNPs were modified with carboxyl functionalized PEG via dopamine (DPA) linker. • Modified and unmodified Fe_3O_4 nanoparticles exhibited super paramagnetic behavior. • T_2 decrease as MNPs concentration increase, this led to MR signal enhancement. • Modified

  18. S tudies on the phase transitions and properties of tungsten (VI oxide nanoparticles by X - Ray diffraction (XRD and thermal analysis

    Directory of Open Access Journals (Sweden)

    S.F. Abdullah

    2017-11-01

    Full Text Available Tungsten (VI oxide, WO3nanoparticles were synthesized by colloidal gas aphrons(CGAs technique.The resultant WO3nanoparticleswere characterized by thermogravimetric-differential thermal analysis (TG-DTA and X-Ray diffraction (XRD measurements in order to determine the phase transitions, the crystallinity and the size of theWO3nanoparticles. As a comparison, transmission electron microscope (TEM was used to investigate the size of the WO3nanoparticles. The result from XRD and DTA show that the formation of polymorphsWO3nanoparticles have the following sequence: orthorhombic (b-WO3®monoclinic (g-WO3 ®triclinic (d-WO3 ®monoclinic (e-WO3 with respect to the calcination temperature of 400, 500, 600 and 700°C. No diffraction peaks were found in the X-Ray diffraction measurements for the sample heat treated at 300°C (as-prepared, suggesting that an amorphous structure was obtained at this temperature whereas the crystallinity had been obtained by the other samples of theWO3nanoparticles at the calcination temperatures of 400, 500, 600 and 700°C. It is also found that the X-Ray diffraction measurements produced an average diameter of (30 ±5, (50 ±5, (150 ±10 and (200 ±10 nm at calcination temperatures of 400, 500, 600 and 700°C respectively by using Debye-Scherrer formula. The TG curve revealed that the WO3nanoparticles is purely anhydrous since the weight loss is insignificant (0.3 –1.4 % from 30 until 600°C for the WO3nanoparticles calcined at 400°C. Finally, the composition and the purity of the WO3nanoparticleshave been examined by X-Ray photoelectron spectroscopy (XPS. Theresults indicate no significant changes to the composition and the purity of the WO3nanoparticle produced due to the temperature variations

  19. Preparation of WO3/g-C3N4 composites and their application in oxidative desulfurization

    International Nuclear Information System (INIS)

    Zhao, Rongxiang; Li, Xiuping; Su, Jianxun; Gao, Xiaohan

    2017-01-01

    Highlights: • The WO 3 /g-C 3 N 4 was successfully synthesized through simple calcination. • The process is simple and the cost raw materials is cheap. • The WO 3 /g-C 3 N 4 firstly applied to ODS. • The desulpurization rate of WO 3 /g-C 3 N 4 may attach to 91.2%. • Five recycles of WO 3 /g-C 3 N 4 still attach to 89.5% due to heterogeneous catalysis. - Abstract: WO 3 /graphitic carbon nitride (g-C 3 N 4 ) composites were successfully synthesized through direct calcining of a mixture of WO 3 and g-C 3 N 4 at 400 °C for 2 h. The WO 3 was prepared by calcination of phosphotungstic acid at 550 °C for 4 h, and the g-C 3 N 4 was obtained by calcination of melamine at 520 °C for 4 h. The WO 3 /g-C 3 N 4 composites were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), and Brunner−Emmett−Teller analysis (BET). The WO 3 /g-C 3 N 4 composites exhibited stronger XRD peaks of WO 3 and g-C 3 N 4 than the WO 3 and pure g-C 3 N 4 . In addition, two WO 3 peaks at 25.7° and 26.6° emerged for the 36% −WO 3 /g-C 3 N 4 composite. This finding indicated that WO 3 was highly dispersed on the surface of the g-C 3 N 4 nanosheets and interacted with the nanosheets, which resulted in the appearance of (012) and (022) planes of WO 3 . The WO 3 /g-C 3 N 4 composite also exhibited a larger specific surface area and higher degree of crystallization than WO 3 or pure g-C 3 N 4 , which resulted in high catalytic activity of the catalyst. Desulfurization experiments demonstrated that the desulfurization rate of dibenzothiophene (DBT) in model oil reached 91.2% under optimal conditions. Moreover, the activity of the catalyst was not significantly decreased after five recycles.

  20. Alginate submicron beads prepared through w/o emulsification and gelation with CaCl2 nanoparticles

    NARCIS (Netherlands)

    Paques, J.P.; Linden, van der E.; Rijn, van C.J.M.; Sagis, L.M.C.

    2013-01-01

    A simple method for preparing gelled alginate beads with a diameter smaller than 5 µm is described. A 1% alginate solution and a medium chain triglyceride (MCT) oil are used to prepare a water-in-oil (w/o) emulsion, stabilized by polyglycerol polyricinoleate. CaCl2 nanoparticles with dimensions in

  1. Enhanced NO2 sensing characteristics of Au modified porous silicon/thorn-sphere-like tungsten oxide composites

    Science.gov (United States)

    Yuan, Lin; Hu, Ming; Wei, Yulong; Ma, Wenfeng

    2016-12-01

    The thorn-sphere-like tungsten oxide (WO3) made up by 1D nanorods has been successfully synthesized through hydrothermal method on the Au-modified porous silicon (PS) substrates with seed-layer induction. By using XRD, EDS, FESEM and TEM techniques, we tested and verified that the crystal structure and morphology evolution of WO3 hierarchical nanostructure on the Au-modified PS strongly depend on the Au-sputtering time and hydrothermal reaction time. In addition, by comparing the NO2-sensing properties of the prepared products, we found that the 10 s-Au decorated PS/WO3-3 h (sputtering Au for 10 s and hydrothermal reaction for 3 h) composites sensor behaving as a typical p-type semiconductor and operating at room temperature (RT) exhibits high sensitivity and response characteristics even to ppb-level NO2, which makes this kind of sensor a competitive candidate for NO2-sensing applications. Moreover, the enhanced response may not only due to the high specific surface area but the Au nanoparticles acting as promoters for the spillover effect and forming metal-semiconductor heterojunctions with the PS and WO3. The transmission of electrons and holes in the heterogeneous interface generated among PS, WO3 and Au is proposed to illustrate the p-type response mechanism.

  2. Dual-Mode SERS-Fluorescence Immunoassay Using Graphene Quantum Dot Labeling on One-Dimensional Aligned Magnetoplasmonic Nanoparticles.

    Science.gov (United States)

    Zou, Fengming; Zhou, Hongjian; Tan, Tran Van; Kim, Jeonghyo; Koh, Kwangnak; Lee, Jaebeom

    2015-06-10

    A novel dual-mode immunoassay based on surface-enhanced Raman scattering (SERS) and fluorescence was designed using graphene quantum dot (GQD) labels to detect a tuberculosis (TB) antigen, CFP-10, via a newly developed sensing platform of linearly aligned magnetoplasmonic (MagPlas) nanoparticles (NPs). The GQDs were excellent bilabeling materials for simultaneous Raman scattering and photoluminescence (PL). The one-dimensional (1D) alignment of MagPlas NPs simplified the immunoassay process and enabled fast, enhanced signal transduction. With a sandwich-type immunoassay using dual-mode nanoprobes, both SERS signals and fluorescence images were recognized in a highly sensitive and selective manner with a detection limit of 0.0511 pg mL(-1).

  3. Conduction and transport numbers in metacomposites MeWO4 · WO3 (Me = Ca, Sr, Ba)

    International Nuclear Information System (INIS)

    Nejman, A.Ya.; Pestereva, N.N.; Sharafutdinov, A.R.; Kostikov, Yu.P.

    2005-01-01

    The conductivity and transfer numbers of charge carriers for composites in the MeWO 4 -WO 3 (Me = Ca, Sr, Ba) systems are studied as a function of the temperature and the activity of oxygen in a gas phase. The transfer numbers are determined by the emf method and are estimated from dependences of conductivity on the activity of oxygen in a gas phase. The deficiencies of the given procedure as applied to investigation of properties of composite phases are analyzed. The materials under study are classified as metacomposites. The concentration intervals of the ionic, mixed, and electronic conductivities are determined. The conductivity of (100-x)MeWO 4 · xWO 3 composites is predominantly ionic at x ≤ 10 (Me = Ca), x ≤ 60 (Me = Sr), and x ≤ 45 (Me = Ba). The obtained data are explained in the framework of a model that represents a composite as a distributed matrix system where a film of surface phase MeW-s with a high mobility of oxygen ions plays the role of a connected matrix. It is presumed that the surface phase MeW-s possesses double-sided surface activity (α MeW-s ≤ α WO 3 , α MeWO 4 ) and a higher mobility with respect to MeWO 4 and WO 3 . The discovered anomalies of dependences σ O 2- (T) and partial conductivities σ O 2- , σ el (T) are explained by a change in the stoichiometry, morphology, and the degree of tie-up of surface phase MeW-s caused by a change in the temperature and composition of composites [ru

  4. First application of a microsphere-based immunoassay to the detection of genetically modified organisms (GMOs): quantification of Cry1Ab protein in genetically modified maize.

    Science.gov (United States)

    Fantozzi, Anna; Ermolli, Monica; Marini, Massimiliano; Scotti, Domenico; Balla, Branko; Querci, Maddalena; Langrell, Stephen R H; Van den Eede, Guy

    2007-02-21

    An innovative covalent microsphere immunoassay, based on the usage of fluorescent beads coupled to a specific antibody, was developed for the quantification of the endotoxin Cry1Ab present in MON810 and Bt11 genetically modified (GM) maize lines. In particular, a specific protocol was developed to assess the presence of Cry1Ab in a very broad range of GM maize concentrations, from 0.1 to 100% [weight of genetically modified organism (GMO)/weight]. Test linearity was achieved in the range of values from 0.1 to 3%, whereas fluorescence signal increased following a nonlinear model, reaching a plateau at 25%. The limits of detection and quantification were equal to 0.018 and 0.054%, respectively. The present study describes the first application of quantitative high-throughput immunoassays in GMO analysis.

  5. Preparation of WO3/g-C3N4 composites and their application in oxidative desulfurization

    Science.gov (United States)

    Zhao, Rongxiang; Li, Xiuping; Su, Jianxun; Gao, Xiaohan

    2017-01-01

    WO3/graphitic carbon nitride (g-C3N4) composites were successfully synthesized through direct calcining of a mixture of WO3 and g-C3N4 at 400 °C for 2 h. The WO3 was prepared by calcination of phosphotungstic acid at 550 °C for 4 h, and the g-C3N4 was obtained by calcination of melamine at 520 °C for 4 h. The WO3/g-C3N4 composites were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), and Brunner-Emmett-Teller analysis (BET). The WO3/g-C3N4 composites exhibited stronger XRD peaks of WO3 and g-C3N4 than the WO3 and pure g-C3N4. In addition, two WO3 peaks at 25.7° and 26.6° emerged for the 36% -WO3/g-C3N4 composite. This finding indicated that WO3 was highly dispersed on the surface of the g-C3N4 nanosheets and interacted with the nanosheets, which resulted in the appearance of (012) and (022) planes of WO3. The WO3/g-C3N4 composite also exhibited a larger specific surface area and higher degree of crystallization than WO3 or pure g-C3N4, which resulted in high catalytic activity of the catalyst. Desulfurization experiments demonstrated that the desulfurization rate of dibenzothiophene (DBT) in model oil reached 91.2% under optimal conditions. Moreover, the activity of the catalyst was not significantly decreased after five recycles.

  6. Nutlin-3a and Cytokine Co-loaded Spermine-Modified Acetalated Dextran Nanoparticles for Cancer Chemo-Immunotherapy

    DEFF Research Database (Denmark)

    Bauleth-Ramos, Tomás; Shahbazi, Mohammad-Ali; Liu, Dongfei

    2017-01-01

    The combination of chemo- and immunotherapy represents one promising strategy to overcome the existent challenges in the present-day anticancer therapy. Here, spermine-modified acetalated dextran nanoparticles (Sp-AcDEX NPs), co-loaded with the non-genotoxic molecule Nutlin-3a (Nut3a), and the cy......The combination of chemo- and immunotherapy represents one promising strategy to overcome the existent challenges in the present-day anticancer therapy. Here, spermine-modified acetalated dextran nanoparticles (Sp-AcDEX NPs), co-loaded with the non-genotoxic molecule Nutlin-3a (Nut3a...

  7. Magnetic bead and gold nanoparticle probes based immunoassay for β-casein detection in bovine milk samples.

    Science.gov (United States)

    Li, Y S; Meng, X Y; Zhou, Y; Zhang, Y Y; Meng, X M; Yang, L; Hu, P; Lu, S Y; Ren, H L; Liu, Z S; Wang, X R

    2015-04-15

    In this work, a double-probe based immunoassay was developed for rapid and sensitive determination of β-casein in bovine milk samples. In the method, magnetic beads (MBs), employed as supports for the immobilization of anti-β-casein polyclonal antibody (PAb), were used as the capture probe. Colloidal gold nanoparticles (AuNPs), employed as a bridge for loading anti-β-casein monoclonal antibody (McAb) and horseradish peroxidase (HRP), were used as the amplification probe. The presence of β-casein causes the sandwich structures of MBs-PAb-β-casein-McAb-AuNPs through the interaction between β-casein and the anti-β-casein antibodies. The HRP, used as an enzymatic-amplified tracer, can catalytically oxidize the substrate 3,3',5,5'-tetramethylbenzidine (TMB), generating optical signals that are proportional to the quantity of β-casein. The linear range of the immunoassay was from 6.5 to 1520ngmL(-1). The limit of detection (LOD) was 4.8ngmL(-1) which was 700 times lower than that of MBs-antibody-HRP based immunoassay and 6-7 times lower than that from the microplate-antibody-HRP based assay. The recoveries of β-casein from bovine milk samples were from 95.0% to 104.3% that had a good correlation coefficient (R(2)=0.9956) with those obtained by an official standard Kjeldahl method. For higher sensitivity, simple sample pretreatment and shorter time requirement of the antigen-antibody reaction, the developed immunoassay demonstrated the viability for detection of β-casein in bovine milk samples. Copyright © 2014. Published by Elsevier B.V.

  8. Exploration on anion ordering, optical properties and electronic structure in K3WO3F3 elpasolite

    International Nuclear Information System (INIS)

    Atuchin, V.V.; Isaenko, L.I.; Kesler, V.G.; Lin, Z.S.; Molokeev, M.S.; Yelisseyev, A.P.; Zhurkov, S.A.

    2012-01-01

    Room-temperature modification of potassium oxyfluorotungstate, G2-K 3 WO 3 F 3 , has been prepared by low-temperature chemical route and single crystal growth. Wide optical transparency range of 0.3–9.4 μm and forbidden band gap E g =4.32 eV have been obtained for G2-K 3 WO 3 F 3 crystal. Meanwhile, its electronic structure has been calculated with the first-principles calculations. The good agreement between the theorectical and experimental results have been achieved. Furthermore, G2-K 3 WO 3 F 3 is predicted to possess the relatively large nonlinear optical coefficients. - Graphical abstract: Using the cm-size K 3 WO 3 F 3 crystal (left upper), the transmission spectrum (right upper) and XPS valence electronic states (left lower) were measured, agreed with the ab initio results (right lower). Highlights: ► The cm-size G2-K 3 WO 3 F 3 single crystals are obtained. ► Optical absorption edge and transmission range are defined for G2-K 3 WO 3 F 3 crystal. ► Crystal structures of all known K 3 WO 3 F 3 polymorph modifications are determined. ► Experimental electronic structure is consistent with the first-principles result. ► G2-K 3 WO 3 F 3 is predicted as a crystal with large NLO coefficients.

  9. Intrinsic Defects and H Doping in WO3

    KAUST Repository

    Zhu, Jiajie; Vasilopoulou, Maria; Davazoglou, Dimitris; Kennou, Stella; Chroneos, Alexander; Schwingenschlö gl, Udo

    2017-01-01

    WO3 is widely used as industrial catalyst. Intrinsic and/or extrinsic defects can tune the electronic properties and extend applications to gas sensors and optoelectonics. However, H doping is a challenge to WO3, the relevant mechanisms being hardly

  10. Characterization of nanosized Al2(WO4)3

    International Nuclear Information System (INIS)

    Nihtianova, D.; Velichkova, N.; Nikolova, R.; Koseva, I.; Yordanova, A.; Nikolov, V.

    2011-01-01

    Graphical abstract: TEM method allows to detect small quantities of impurities not detectable by other methods. In our case impurities of W 5 O 14 are detected in Al 2 (WO 4 ) 3 nanopowder. Highlights: → Nanosized Al 2 (WO 4 ) 3 by simple co-precipitation method. → Spherical particles with mean size of 22 nm distributed between 10 and 40 nm at 630 o C. → XRD, DTA and TEM confirm well defined products with perfect structure. → TEM locality allows detection of impurities not detectable by XRD and DTA. -- Abstract: Nanosized aluminum tungstate Al 2 (WO 4 ) 3 was prepared by co-precipitation reaction between Na 2 WO 4 and Al(NO 3 ) 3 aqueous solutions. The powder size and shape, as well as size distribution are estimated after different conditions of powder preparation. The purity of the final product was investigated by XRD and DTA analyses, using the single crystal powder as reference. Between the specimen and the reference no difference was detected. The crystal structure of Al 2 (WO 4 ) 3 nanosized powder was confirmed by TEM (SAED, HRTEM). In additional, TEM locality allows to detect some W 5 O 14 impurities, which are not visible by conventional X-ray powder diffraction and thermal analyses.

  11. Preparation, characterization and SRXPS study of polyvinyl alcohol modified Fe3O4 nanoparticles

    International Nuclear Information System (INIS)

    Li Ming; Wang Bing; Feng Weiyue; Liu Hui; Kang Yanjie; Kui Rexi

    2011-01-01

    In this study, Fe 3 O 4 nanoparticles were coated with PVA to synthesize PVA-Fe 3 O 4 complex, which were characterized by transmission electron microscopy(TEM),thermo gravimetric(TG) analysis, UV-vis spectra,zeta potentials and ICP-MS, in terms of the physicochemical properties, while surface constituents, structures and chemical bonds of the modified and unmodified nanoparticles were characterized with synchrotron radiation X-ray photoelectron spectroscopy(SRXPS), for exploring modification mechanism of the PVA-Fe 3 O 4 . The results indicate that after PVA modification, the suspension stability of Fe 3 O 4 nanoparticles in water and cellular uptake capability were significantly improved compared with unmodified Fe 3 O 4 . The SRXPS analysis reveals that the hydroxy groups on the surface of Fe 3 O 4 nanoparticles and PVA were combined by hydrogen bond to consist a stable system, which would be beneficial to the biomedical applications of Fe 3 O 4 nanoparticles. (authors)

  12. Enhanced photocatalytic activity of cadmium-doped Bi{sub 2}WO{sub 6} nanoparticles under simulated solar light

    Energy Technology Data Exchange (ETDEWEB)

    Song, Xu Chun, E-mail: songxuchunfj@163.com; Li, Wen Ting [Fujian Normal University, Department of Chemistry (China); Huang, Wan Zhen; Zhou, Huan [Zhejiang University of Technology, Research Center of Analysis and Measurement (China); Yin, Hao Yong [Hangzhou Dianzi University, Institute of Environmental Science and Engineering (China); Zheng, Yi Fan [Zhejiang University of Technology, Research Center of Analysis and Measurement (China)

    2015-03-15

    Novel cadmium-doped Bi{sub 2}WO{sub 6} nanoparticles with different Cd contents have been synthesized by a one-step route using ethylene glycol and water as solvents at 180 °C for 12 h. The as-synthesized samples were characterized in detailed by SEM, XRD, EDS, HRTEM, UV–Vis DRS, BET techniques, and so on. The results shown that with the increase of the Cd{sup 2+} addition, the crystal structure, lattice space, and absorption edge were not significantly changed and the calculated band gap value was 2.58 eV. However, the flower-like Bi{sub 2}WO{sub 6} sphere was gradually destroyed. Simultaneously, the surface area and photocurrent responses of the catalysts were greatly increased. Photocatalytic activity of the Cd-doped Bi{sub 2}WO{sub 6} samples was determined by monitoring the change of RhB concentration under simulated solar light. The results revealed that cadmium doping greatly improved the photocatalytic efficiency of Bi{sub 2}WO{sub 6}. The Bi{sub 2}WO{sub 6} sample with R{sub Cd} = 0.05 displayed the highest photocatalytic activity, and the degradation rate is about two times greater than pure Bi{sub 2}WO{sub 6}. Moreover, the Cd–Bi{sub 2}WO{sub 6} photocatalyst remained stable even after five consecutive cycles. A possible mechanism of photocatalytic activity enhancement on basis of the experimental results was proposed.

  13. Characterization and application of a new pH sensor based on magnetron sputtered porous WO3 thin films deposited at oblique angles

    International Nuclear Information System (INIS)

    Salazar, Pedro; Garcia-Garcia, Francisco J.; Yubero, Francisco; Gil-Rostra, Jorge; González-Elipe, Agustín R.

    2016-01-01

    Highlights: • A solid-state pH sensor based on WO 3 amorphous thin film electrode is reported. • Cyclic voltammetry and XRD confirmed the amorphous nature of tungsten. • Potentiometric response of the WO 3 electrode revealed a quasi-Nernstian behavior. • The interference of the most common ions (Li + , Na + , K + and NH 4 + ) was negligible. • A full solid state pH sensor is developed. - Abstract: In this communication we report about an outstanding solid-state pH sensor based on amorphous nanocolumnar porous thin film electrodes. Transparent WO 3 thin films were deposited by reactive magnetron sputtering in an oblique angle configuration to enhance their porosity onto indium tin oxide (ITO) and screen printed electrodes (SPE). The potentiometric pH response of the nanoporous WO 3 -modified ITO electrode revealed a quasi-Nernstian behaviour, i.e. a linear working range from pH 1 to 12 with a slope of about −57.7 mV/pH. pH detection with this electrode was quite reproducible, displayed excellent anti-interference properties and a high stable response that remained unaltered over at least 3 months. Finally, a pH sensor was developed using nanoporous WO 3 -modified screen printed electrode (SPE) using a polypyrrole-modified Ag/AgCl electrode as internal reference electrode. This full solid state pH sensor presented a Nernstian behaviour with a slope of about −59 mV/pH and offered important analytical and operation advantages for decentralized pH measurements in different applications.

  14. Monodisperse magnetite (Fe{sub 3}O{sub 4}) nanoparticles modified with water soluble polymers for the diagnosis of breast cancer by MRI method

    Energy Technology Data Exchange (ETDEWEB)

    Rezayan, Ali Hossein, E-mail: ahrezayan@ut.ac.ir [Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran (Iran, Islamic Republic of); Mousavi, Majid [Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran (Iran, Islamic Republic of); Kheirjou, Somayyeh [Department of Chemistry, Sharif University of Technology, Tehran (Iran, Islamic Republic of); Amoabediny, Ghasem [School of Chemical Engineering, College of Engineering, University of Tehran, Tehran (Iran, Islamic Republic of); Ardestani, Mehdi Shafiee [Department of Pharmacy, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Mohammadnejad, Javad [Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran (Iran, Islamic Republic of)

    2016-12-15

    In this study, magnetic nanoparticles (MNPs) were synthesized via co-precipitation method. To enhance the biocompatibility and colloidal stability of the synthesized nanoparticles, they were modified with carboxyl functionalized PEG via dopamine (DPA) linker. Both modified and unmodified Fe{sub 3}O{sub 4} nanoparticles exhibited super paramagnetic behavior (particle size below 20 nm). The saturation magnetization (Ms) of PEGdiacid-modified Fe{sub 3}O{sub 4} was 45 emu/g, which was less than the unmodified Fe{sub 3}O{sub 4} nanoparticles (70 emu/g). This difference indicated that PEGdiacid polymer was immobilized on the surface of Fe{sub 3}O{sub 4} nanoparticles successfully. To evaluate the efficiency of the resulting nanoparticles as contrast agents for magnetic resonance imaging (MRI), different concentration of MNPs and different value of echo time TE were investigated. The results showed that by increasing the concentration of the nanoparticles, transverse relaxation time (T{sub 2}) decreased, which subsequently resulted in MR signal enhancement. T{sub 2}-weighted MR images of the different concentration of MNPs in different value of echo time TE indicated that MR signal intensity increased with increase in TE value up to 66 and then remained constant. The cytotoxicity effect of the modified and unmodified nanoparticles was evaluated in three different concentrations (12, 60 and 312 mg l{sup −1}) on MDA-MB-231 cancer cells for 24 and 48 h. In both tested time (24 and 48 h) for all three samples, the modified nanoparticles had long life time than unmodified nanoparticles. Cellular uptake of modified MNPs was 80% and reduced to 9% by the unmodified MNPs. - Highlights: • Magnetic nanoparticles (MNPs) were synthesized via co-precipitation method. • MNPs were modified with carboxyl functionalized PEG via dopamine (DPA) linker. • Modified and unmodified Fe{sub 3}O{sub 4} nanoparticles exhibited super paramagnetic behavior. • T{sub 2} decrease as MNPs

  15. WO{sub 3} nanorods prepared by low-temperature seeded growth hydrothermal reaction

    Energy Technology Data Exchange (ETDEWEB)

    Ng, Chai Yan [School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Abdul Razak, Khairunisak, E-mail: khairunisak@eng.usm.my [School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); NanoBiotechnology Research and Innovation (NanoBRI), Institute for Research in Molecular Medicine (INFORMM), Universiti Sains Malaysia, 11800 USM, Penang (Malaysia); Lockman, Zainovia, E-mail: zainovia@eng.usm.my [School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia)

    2014-03-05

    Highlights: • WO{sub 3} nanorods with 5–10 nm diameter were grown directly on seeded tungsten foil. • WO{sub 3} nanorods were successfully grown at low temperature of 80 °C. • WO{sub 3} nanorods were grown on the entire surface of the seed layer after 24 h. • Annealed nanorods showed better electrochromic properties than as-made nanorods. -- Abstract: This work describes the first tungsten oxide (WO{sub 3}) nanorods hydrothermally grown on W foil. WO{sub 3} nanorods were successfully grown at low hydrothermal temperature of 80 °C by seeded growth hydrothermal reaction. The seed layer was prepared by thermally oxidized the W foil at 400 °C for 0.5 h. This work discusses the effect of hydrothermal reaction and annealing period on the morphological, structural, and electrochromic properties of WO{sub 3} nanorods. Various hydrothermal reaction periods (8–24 h) were studied. Monoclinic WO{sub 3} nanorods with 5–10 nm diameter were obtained after hydrothermal reaction for 24 h. These 24 h WO{sub 3} nanorods were also annealed at 400 °C with varying dwelling periods (0.5–4 h). Electrochromic properties of WO{sub 3} nanorods in an acidic electrolyte were analyzed using cyclic voltammetry and UV–vis spectrophotometry. WO{sub 3} nanorods annealed at 400 °C for 1 h showed the highest charge capacity and the largest optical contrast among the 24 h WO{sub 3} films. The sample also showed good cycling stability without significant degradation. Based on the results, the reaction mechanism of WO{sub 3} nanorod formation on W foil was proposed.

  16. Oxidative degradation of salicylic acid by sprayed WO{sub 3} photocatalyst

    Energy Technology Data Exchange (ETDEWEB)

    Mohite, S.V.; Rajpure, K.Y., E-mail: rajpure@yahoo.com

    2015-10-15

    Highlights: • The photoactivity of sprayed WO{sub 3} thin film. • Photoelectrocatalytic degradation of salicylic acid. • Reaction kinetics and mineralization of pollutants by COD. - Abstract: The WO{sub 3} thin films were deposited using spray pyrolysis technique. The prepared WO{sub 3} thin films were characterized using photoelectrochemical (PEC), X-ray diffraction, atomic force microscopy (AFM), and UV–vis absorbance spectroscopy techniques. PEC measurements of WO{sub 3} films deposited at different deposition temperatures were carried out to study photoresponse. The maximum photocurrent (I{sub ph} = 261 μA/cm{sup 2}) was observed for the film deposited at the 225 °C. The monoclinic crystal structure of WO{sub 3} has been confirmed from X-ray diffraction studies. AFM studies were used to calculate particle size and average roughness of the films. Optical absorbance was studied to estimate the bandgap energy of WO{sub 3} thin film which was about 2.65 eV. The photoelectrocatalytic activity of WO{sub 3} film was studied by degradation of salicylic acid with reducing concentrations as function of reaction time. The WO{sub 3} photocatalyst degraded salicylic acid to about 67.14% with significant reduction in chemical oxygen demand (COD) value.

  17. Design and preparation of bi-functionalized short-chain modified zwitterionic nanoparticles.

    Science.gov (United States)

    Hu, Fenglin; Chen, Kaimin; Xu, Hong; Gu, Hongchen

    2018-05-01

    An ideal nanomaterial for use in the bio-medical field should have a distinctive surface capable of effectively preventing nonspecific protein adsorption and identifying target bio-molecules. Recently, the short-chain zwitterion strategy has been suggested as a simple and novel approach to create outstanding anti-fouling surfaces. In this paper, the carboxyl end group of short-chain zwitterion-coated silica nanoparticles (SiO 2 -ZWS) was found to be difficult to functionalize via a conventional EDC/NHS strategy due to its rapid hydrolysis side-reactions. Hence, a series of bi-functionalized silica nanoparticles (SiO 2 -ZWS/COOH) were designed and prepared by controlling the molar ratio of 3-aminopropyltriethoxysilane (APTES) to short-chain zwitterionic organosiloxane (ZWS) in order to achieve above goal. The synthesized SiO 2 -ZWS/COOH had similar excellent anti-fouling properties compared with SiO 2 -ZWS, even in 50% fetal bovine serum characterized by DLS and turbidimetric titration. Subsequently, SiO 2 -ZWS/COOH 5/1 was chosen as a representative and then demonstrated higher detection signal intensity and more superior signal-to-noise ratios compare with the pure SiO 2 -COOH when they were used as a bio-carrier for chemiluminescence enzyme immunoassay (CLEIA). These unique bi-functionalized silica nanoparticles have many potential applications in the diagnostic and therapeutic fields. Reducing nonspecific protein adsorption and enhancing the immobilized efficiency of specific bio-probes are two of the most important issues for bio-carriers, particularly for a nanoparticle based bio-carrier. Herein, we designed and prepared a bi-functional nanoparticle with anti-fouling property and bio conjugation capacity for further bioassay by improving the short-chain zwitterionic modification strategy we have proposed previously. The heterogeneous surface of this nanoparticle showed effective anti-fouling properties both in model protein solutions and fetal bovine serum

  18. Solid-Phase Immunoassay of Polystyrene-Encapsulated Semiconductor Coreshells for Cardiac Marker Detection

    Directory of Open Access Journals (Sweden)

    Sanghee Kim

    2012-01-01

    Full Text Available A solid-phase immunoassay of polystyrene-encapsulated semiconductor nanoparticles was demonstrated for cardiac troponin I (cTnI detection. CdSe/ZnS coreshells were encapsulated with a carboxyl-functionalized polystyrene nanoparticle to capture the target antibody through a covalent bonding and to eliminate the photoblinking and toxicity of semiconductor luminescent immunosensor. The polystyrene-encapsulated CdSe/ZnS fluorophores on surface-modified glass chip identified cTnI antigens at the level of ~ng/mL. It was an initial demonstration of diagnostic chip for monitoring a cardiovascular disease.

  19. WO3 Nanowires on Graphene Sheets as Negative Electrode for Supercapacitors

    Directory of Open Access Journals (Sweden)

    Bo Liu

    2017-01-01

    Full Text Available WO3 nanowires directly grown on graphene sheets have been fabricated by using a seed-mediated hydrothermal method. The morphologies and electrochemical performance of WO3 films prepared by different process were studied. The results show that the precoated nanoseeds and graphene sheets on graphite electrode provide more reactive centers for the nucleation and formation of uniform WO3 nanowires. The WO3 nanowires electrode exhibits a high area specific capacitance of 800 mF cm−2 over negative potential range from −1.0 V to 0 V versus SCE in 1 M Li2SO4 solution. A high performance electrochemical supercapacitor assembled with WO3 nanowires as negative electrode and PANI/MnO2 as positive electrodes over voltage range of 1.6 V displays a high volumetric capacitance of 2.5 F cm−3, which indicate great potential applications of WO3 nanowires on graphene sheets as negative electrode for energy storage devices.

  20. Improving the sensitivity of immunoassay based on MBA-embedded Au@SiO2 nanoparticles and surface enhanced Raman spectroscopy

    Science.gov (United States)

    Wei, Chao; Xu, Min-Min; Fang, Cong-Wei; Jin, Qi; Yuan, Ya-Xian; Yao, Jian-Lin

    2017-03-01

    Traditional "sandwich" structure immunoassay is mainly based on the self-assembly of "antibody on solid substrate-antigen-antibody with nanotags" architectures, and the sensitivity of this strategy is critically depended on the surface enhanced Raman scattering (SERS) activities and stability of nanotags. Therefore, the rational design and fabrication on the SERS nanotags attracts the common interests to the bio-related detecting and imaging. Herein, silica encapsulated Au with mercaptobenzoic acid (MBA) core-shell nanoparticles (Au-MBA@SiO2) are fabricated instead of the traditional naked Au or Ag nanoparticles for the SERS-based immunoassay on human and mouse IgG antigens. The MBA molecules facilitate the formation of continuous pinhole-free silica shell and are also used as SERS labels. The silica shell is employed to protect MBA labels and to isolate Au core from the ambient solution for blocking the aggregation. This shell also played the similar role to BSA in inhibiting the nonspecific bindings, which allowed the procedures for constructing "sandwich" structures to be simplified. All of these merits of the Au-MBA@SiO2 brought the high performance in the related immunoassay. Benefiting from the introduction of silica shell to encapsulate MBA labels, the detection sensitivity was improved by about 1- 2 orders of magnitude by comparing with the traditional approach based on naked Au-MBA nanoparticles. This kind of label-embedded core-shell nanoparticles could be developed as the versatile nanotags for the bioanalysis and bioimaging.

  1. Parylene nanocomposites using modified magnetic nanoparticles

    International Nuclear Information System (INIS)

    Garcia, Ignacio; Luzuriaga, A. Ruiz de; Grande, H.; Jeandupeux, L.; Charmet, J.; Laux, E.; Keppner, H.; Mecerreyes, D.; Cabanero, German

    2010-01-01

    Parylene/Fe 3 O 4 nanocomposites were synthesized and characterized. The nanocomposites were obtained by chemical vapour deposition polymerization of Parylene onto functionalized Fe 3 O 4 nanoparticles. For this purpose, allyltrichlorosilane was used to modify the surface of 7 nm size Fe 3 O 4 nanoparticles obtained by the coprecipitation method. The magnetic nanoparticles and obtained nanocomposite were characterized with X-ray diffraction (XRD), infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA) and magnetic measurements (SQUID). The successful incorporation of different amounts of nanoparticles into Parylene was confirmed by FTIR and TGA. Interestingly, increments in saturation magnetization of the nanocomposites were observed ranging from 0 emu/g of neat Parylene to 16.94 emu/g in the case of nanocomposite films that contained 27.5 wt% of nanoparticles.

  2. Facile preparation of hexagonal WO{sub 3}·0.33H{sub 2}O/C nanostructures and its electrochemical properties for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Zhiwei [Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083 (China); Li, Ping, E-mail: ustbliping@126.com [Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083 (China); Dong, Yuan [Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083 (China); Wan, Qi [Energy Material & Technology Research Institute, General Research Institute for Nonferrous Metal, Beijing 100088 (China); Zhai, Fuqiang [Departament Física Aplicada, EETAC, Universitat Politècnica de Catalunya – Barcelona Tech, 08860 Castelldefels (Spain); Volinsky, Alex A. [Department of Mechanical Engineering, University of South Florida, Tampa, FL 33620 (United States); Qu, Xuanhui [Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083 (China)

    2017-02-01

    Highlights: • WO{sub 3}·0.33H{sub 2}O/C was prepared by the facile synthesis & hydrothermal method. • WO{sub 3}·0.33H{sub 2}O/C electrode capacity is higher than the reported orthorhombic WO{sub 3}·0.33H{sub 2}O. • The specific structure can provide efficient channels for the fast transport of Li{sup +}. - Abstract: Nano-sized hexagonal WO{sub 3}·0.33H{sub 2}O/C is prepared by the solution combustion synthesis & hydrothermal method. This material has been used as the anode for high performance lithium-ion batteries for the first time. Carbon layer is uniformly coated on hexagonal WO{sub 3}·0.33H{sub 2}O nanoparticles. The samples are characterized by X-ray diffraction (XRD), thermal analysis (TG-DSC), Raman spectra, scanning and transmission electron microscopy (FESEM and TEM). Electrochemical properties are studied by cyclic voltammetry and galvanostatic charge/discharge cycling. Prepared WO{sub 3}·0.33H{sub 2}O/C electrode shows high and reversible capacity of 768 mAh g{sup −1} after 200 cycles at 100 mA g{sup −1}, which is higher than the reported orthorhombic WO{sub 3}·0.33H{sub 2}O. The specific structure can provide efficient channels for transporting Li{sup +} swiftly. Therefore, hexagonal WO{sub 3}·0.33H{sub 2}O/C shows a great potential as the anode material for lithium-ion batteries.

  3. Electrochromic device based on electrospun WO{sub 3} nanofibers

    Energy Technology Data Exchange (ETDEWEB)

    Dulgerbaki, Cigdem; Maslakci, Neslihan Nohut; Komur, Ali Ihsan; Oksuz, Aysegul Uygun, E-mail: ayseguluygun@sdu.edu.tr

    2015-12-15

    Highlights: • WO{sub 3} electrochromic nanofibers were prepared by electrospinning technique. • WO{sub 3} nanofibers switched reversibly from transparent to blue color. • Electrochromic device was assembled using ionic liquid based gel electrolyte. • Significant optical modulation and excellent cycling stability were achieved for ECD. - Abstract: The tungsten oxide (WO{sub 3}) nanofibers were grown directly onto an ITO-coated glass via an electrospinning method for electrochromic applications. The electrochromic properties of WO{sub 3} nanofibers were investigated in the presence of different electrolytes including a series of ionic liquids and classic LiClO{sub 4}-PC system. A significant optical modulation of 20.82% at 760 nm, reversible coloration with efficiency of 64.58 cm{sup 2}/C and excellent cycling stability were achieved for the nanofiber electrochromic device (ECD) with ionic liquid based gel electrolyte.

  4. Nanoparticles modified with multiple organic acids

    Science.gov (United States)

    Cook, Ronald Lee (Inventor); Luebben, Silvia DeVito (Inventor); Myers, Andrew William (Inventor); Smith, Bryan Matthew (Inventor); Elliott, Brian John (Inventor); Kreutzer, Cory (Inventor); Wilson, Carolina (Inventor); Meiser, Manfred (Inventor)

    2007-01-01

    Surface-modified nanoparticles of boehmite, and methods for preparing the same. Aluminum oxyhydroxide nanoparticles are surface modified by reaction with selected amounts of organic acids. In particular, the nanoparticle surface is modified by reactions with two or more different carboxylic acids, at least one of which is an organic carboxylic acid. The product is a surface modified boehmite nanoparticle that has an inorganic aluminum oxyhydroxide core, or part aluminum oxyhydroxide core and a surface-bonded organic shell. Organic carboxylic acids of this invention contain at least one carboxylic acid group and one carbon-hydrogen bond. One embodiment of this invention provides boehmite nanoparticles that have been surface modified with two or more acids one of which additional carries at least one reactive functional group. Another embodiment of this invention provides boehmite nanoparticles that have been surface modified with multiple acids one of which has molecular weight or average molecular weight greater than or equal to 500 Daltons. Yet, another embodiment of this invention provides boehmite nanoparticles that are surface modified with two or more acids one of which is hydrophobic in nature and has solubility in water of less than 15 by weight. The products of the methods of this invention have specific useful properties when used in mixture with liquids, as filler in solids, or as stand-alone entities.

  5. Nanoparticles modified with multiple organic acids

    Science.gov (United States)

    Cook, Ronald Lee; Luebben, Silvia DeVito; Myers, Andrew William; Smith, Bryan Matthew; Elliott, Brian John; Kreutzer, Cory; Wilson, Carolina; Meiser, Manfred

    2007-07-17

    Surface-modified nanoparticles of boehmite, and methods for preparing the same. Aluminum oxyhydroxide nanoparticles are surface modified by reaction with selected amounts of organic acids. In particular, the nanoparticle surface is modified by reactions with two or more different carboxylic acids, at least one of which is an organic carboxylic acid. The product is a surface modified boehmite nanoparticle that has an inorganic aluminum oxyhydroxide core, or part aluminum oxyhydroxide core and a surface-bonded organic shell. Organic carboxylic acids of this invention contain at least one carboxylic acid group and one carbon-hydrogen bond. One embodiment of this invention provides boehmite nanoparticles that have been surface modified with two or more acids one of which additional carries at least one reactive functional group. Another embodiment of this invention provides boehmite nanoparticles that have been surface modified with multiple acids one of which has molecular weight or average molecular weight greater than or equal to 500 Daltons. Yet, another embodiment of this invention provides boehmite nanoparticles that are surface modified with two or more acids one of which is hydrophobic in nature and has solubility in water of less than 15 by weight. The products of the methods of this invention have specific useful properties when used in mixture with liquids, as filler in solids, or as stand-alone entities.

  6. An ultraviolet photodetector fabricated from WO3 nanodiscs/reduced graphene oxide composite material

    International Nuclear Information System (INIS)

    Shao Dali; Sawyer, Shayla; Yu Mingpeng; Lian Jie

    2013-01-01

    A high sensitivity, fast ultraviolet (UV) photodetector was fabricated from WO 3 nanodiscs (NDs)/reduced graphene oxide (RGO) composite material. The WO 3 NDs/reduced GO composite material was synthesized using a facile three-step synthesis procedure. First, the Na 2 WO 4 /GO precursor was synthesized by homogeneous precipitation. Second, the Na 2 WO 4 /GO precursor was transformed into H 2 WO 4 /GO composites by acidification. Finally, the H 2 WO 4 /GO composites were reduced to WO 3 NDs/RGO via a hydrothermal reduction process. The UV photodetector showed a fast transient response and high responsivity, which are attributed to the improved carrier transport and collection efficiency through graphene. The excellent material properties of the WO 3 NDs/RGO composite demonstrated in this work may open up new possibilities for using WO 3 NDs/RGO for future optoelectronic applications. (paper)

  7. Improving Pullulanase Catalysis via Reversible Immobilization on Modified Fe3O4@Polydopamine Nanoparticles.

    Science.gov (United States)

    Wang, Jianfeng; Liu, Zhongmei; Zhou, Zhemin

    2017-08-01

    To improve the catalysis of pullulanase from Anoxybacillus sp.WB42, Fe 3 O 4 @polydopamine nanoparticles (Fe 3 O 4 @PDA) were prepared and modified with functional groups for immobilization of pullulanases via covalent binding or ionic adsorption. Immobilized pullulanases had lower thermal stability than that of free pullulanase, whereas their catalysis depended on the surface characteristics of nanoparticles. As for covalent immobilization of pullulanases onto Fe 3 O 4 @PDA derivatives, the spacer grafted onto Fe 3 O 4 @PDA made the catalytic efficiency of pullulanase increase up to the equivalence of free enzyme but dramatically reduced the pullulanase thermostability. In contrast, pullulanases bounded ionically to Fe 3 O 4 @PDA derivatives had higher activity recovery and catalytic efficiency, and their catalytic behaviors varied with the modifier grafted onto Fe 3 O 4 @PDA. Among these immobilized pullulanases, ionic adsorption of pullulanase on Fe 3 O 4 @PDA-polyethyleneimine-glycidyltrimethylammonium gave a high-performance and durable catalyst, which displayed not only 1.5-fold increase in catalytic efficiency compared to free enzyme but also a significant improvement in operation stability with a half of initial activity after 27 consecutive cycles with a total reaction time of 13.5 h, and was reversible, making this nanoparticle reusable for immobilization.

  8. Enhanced structural and optical properties of the polyaniline-calcium tungstate (PANI-CaWO4 nanocomposite for electronics applications

    Science.gov (United States)

    Sabu, N. Aloysius; Francis, Xavier; Anjaly, Jose; Sankararaman, S.; Varghese, Thomas

    2017-06-01

    In this article, we report the synthesis and characterization of polyaniline-calcium tungstate nanocomposite, a novel material for potential applications. The PANI-CaWO4 nanocomposite was prepared by in situ oxidative polymerization of aniline in the presence of CaWO4 nanoparticles dispersed in ethanol. Investigations using X-ray diffraction, Fourier-transformed infrared spectroscopy, UV-visible, photoluminescence and Raman spectroscopy confirmed the formation of the nanocomposite of PANI with CaWO4 nanoparticles. Scanning electron microscopy revealed almost uniform distribution of CaWO4 nanoparticles in the polyaniline matrix. These studies also confirmed electronic structure modification as a result of incorporating CaWO4 nanoparticles in PANI. Composite formation resulted in large decrease in the optical band gap and enhanced photoluminescence. The augmented structural, optical and photoluminescence properties of the PANI-CaWO4 nanocomposite can be used to explore potential applications in micro- and optoelectronics. This is the first report presenting synthesis and characterization of the PANI-CaWO4 nanocomposite.

  9. Electrical, thermophysical and micromechanical properties of ethylene-vinyl acetate elastomer composites with surface modified BaTiO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Huang Xingyi; Xie Liyuan; Jiang Pingkai; Wang Genlin; Liu Fei, E-mail: xyhuang@sjtu.edu.c, E-mail: pkjiang@sjtu.edu.c [Shanghai Key Lab of Electrical Insulation and Thermal Aging, Department of Polymer Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China)

    2009-12-21

    In this study, we investigated the influence of the surface modified BaTiO{sub 3} nanoparticles on the electrical, thermophysical and micromechanical properties of ethylene-vinyl acetate (EVM) vulcanizates. Gamma-aminopropyl triethoxysilane was used as a silane coupling agent for the surface treatment of the BaTiO{sub 3} nanoparticles. It was found that the incorporation of surface modified BaTiO{sub 3} nanoparticles into the EVM matrix not only increased the permittivity, thermal conductivity and the mechanical strength but also showed a comparative dielectric loss tangent with pure EVM vulcanizates. In particular, the nanocomposites exhibit relatively high dielectric strength and good ductility even at the loading level of 50 vol%. The improved properties not only originate from the homogeneous dispersion of BaTiO{sub 3} nanoparticles but also should be ascribed to the strong interfacial interaction between the surface modified BaTiO{sub 3} nanoparticles and EVM matrix. We also investigated the dielectric relaxation behaviour of the BaTiO{sub 3} filled EVM nanocomposites by using Jonscher's theory of universal dielectric response.

  10. CTAB-assisted ultrasonic synthesis, characterization and photocatalytic properties of WO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Sánchez-Martínez, D., E-mail: dansanm@gmail.com; Gomez-Solis, C.; Torres-Martinez, Leticia M.

    2015-01-15

    Highlights: • WO{sub 3} 2D nanostructures were synthesized by ultrasound method assisted with CTAB. • WO{sub 3} morphology was mainly of rectangular nanoplates with a thickness of ∼50 nm. • The highest surface area value of WO{sub 3} was obtained to lowest concentration of CTAB. • WO{sub 3} activity was attributed to morphology, surface area and the addition of CTAB. • WO{sub 3} nanoplates were able to causing almost complete mineralization of rhB and IC. - Abstract: WO{sub 3} 2D nanostructures have been prepared by ultrasound synthesis method assisted with CTAB using different molar ratios. The formation of monoclinic crystal structure of WO{sub 3} was confirmed by X-ray powder diffraction (XRD). The characterization of the WO{sub 3} samples was complemented by analysis of scanning electron microscopy (SEM), which revealed morphology mainly of rectangular nanoplates with a thickness of around 50 nm and length of 100–500 nm. Infrared spectroscopy (FT-IR) was used to confirm the elimination of the CTAB in the synthesized samples. The specific surface area was determinate by the BET method and by means of diffuse reflectance spectroscopy (DRS) it was determinate the band-gap energy (E{sub g}) of the WO{sub 3} samples. The photocatalytic activity of the WO{sub 3} oxide was evaluated in the degradation reactions of rhodamine B (rhB) and indigo carmine (IC) under Xenon lamp irradiation. The highest photocatalytic activity was observed in the samples containing low concentration of CTAB with morphology of rectangular nanoplates and with higher surface area value than commercial WO{sub 3}. Photodegradation of rhB and IC were followed by means of UV–vis absorption spectra. The mineralization degree of organic dyes by WO{sub 3} photocatalyst was determined by total organic carbon analysis (TOC) reaching percentages of mineralization of 92% for rhB and 50% for IC after 96 h of lamp irradiation.

  11. In situ loading of Ag_2WO_4 on ultrathin g-C_3N_4 nanosheets with highly enhanced photocatalytic performance

    International Nuclear Information System (INIS)

    Li, Yunfeng; Jin, Renxi; Fang, Xu; Yang, Yang; Yang, Man; Liu, Xianchun; Xing, Yan; Song, Shuyan

    2016-01-01

    Graphical abstract: Ultrathin g-C_3N_4 nanosheets (g-C_3N_4−NS) with improved electron transport ability and large number of active sites are employed instead of bulk g-C_3N_4 to prepare the Ag_2WO_4/g-C_3N_4−NS heterostructured photocatalysts, which exhibit remarkable photocatalytic activity for wastewater treatment. - Highlights: • Ag2WO4/g-C3N4-NS photocatalysts were obtained by a deposition-precipitation method. • Ag2WO4/g-C3N4-NS possess large surface areas and increased lifetime of charges. • Ag2WO4/g-C3N4-NS exhibit enhanced activity on degradation of RhB and MO. • The photocatalytic mechanism of the Ag2WO4/g-C3N4-NS system were investigated. - Abstract: The g-C_3N_4 nanosheets (g-C_3N_4−NS) exhibit more excellent property than common bulk g-C_3N_4 (g-C_3N_4-B) due to their large surface areas, improved electron transport ability and well dispersion in water. In this work, ultrathin g-C_3N_4−NS with a thickness of about 2.7 nm have been synthesized by a simple thermal exfoliation of bulk g-C_3N_4, and then Ag_2WO_4 nanoparticles are in situ loaded on their surface to construct the Ag_2WO_4/g-C_3N_4−NS heterostructured photocatalysts. Due to their unique physicochemical properties, the as-prepared heterostructures possess a fast interfacial charge transfer and increased lifetime of photo-excited charge carriers, and exhibit much higher photocatalytic activity. Under visible light irradiation, the optimum photocatalytic activity of Ag_2WO_4/g-C_3N_4−NS composites is almost 53.6 and 26.5 times higher than that of pure g-C_3N_4-B and Ag_2WO_4/g-C_3N_4-B heterostructures towards the degradation of rhodamine B, respectively, and is almost 30.6 and 9.8 times higher towards the degradation of methyl orange, respectively. In addition, the natural sunlight photocatalytic activities of the as-prepared samples are also investigated.

  12. Screening for cystic fibrosis via a magnetic and microfluidic immunoassay format with electrochemical detection using a copper nanoparticle-modified gold electrode

    International Nuclear Information System (INIS)

    Benuzzi, Maria Luz Scala; Pereira, Sirley V.; Raba, Julio; Messina, Germán A.

    2016-01-01

    This article describes a microfluidic electrochemical immunoassay that features two strategies, viz. (a), the incorporation of magnetic nanoparticles (MNPs) into the central microfluidic channel and acting as a bioaffinity support for the immobilization of the antibody against the immunoreactive trypsin (anti-IRT), and (b), the electrodeposition of copper nanoparticles (CuNPs) on a gold electrode. IRT, a marker for cystic fibrosis, is extracted from blood samples onto a disk using ultrasonication, eluted, and then injected into the detection system where it is captured by anti-IRT-loaded nanoparticles (anti-IRT-Ab-MNPs). Bound IRT is electrochemically quantified after addition of HRP-labeled anti-IRT-Ab which, in the presence of H 2 O 2 , catalyzes the oxidation of catechol to form o-benzoquinone which is detected at a working potential of −1 50 mV (vs. Ag/AgCl). The electrochemical response to benzoquinone is proportional to the concentration of IRT in the range from 0 to 580 ng⋅mL −1 . The coefficients of variation are <5 % for within-day assays, and <6.4 % for between-day assays. The method was compared to a commercial ELISA for IRT where is showed a correlation coefficient of close to 1. In our perception, this approach represents an attractive alternative to existing methods for screening newborns for cystic fibrosis. (author)

  13. Photocatalytic activity of Bi_2WO_6/Bi_2S_3 heterojunctions: the facilitation of exposed facets of Bi_2WO_6 substrate

    International Nuclear Information System (INIS)

    Yan, Long; Wang, Yufei; Shen, Huidong; Zhang, Yu; Li, Jian; Wang, Danjun

    2017-01-01

    Highlights: • Bi_2S_3/Bi_2WO_6 hybrids with exposed (020) Bi_2WO_6 facets have been synthesized. • X-ray photoelectron spectroscopy reveals that a small amount of Bi_2S_3 was formed. • The enhanced photoactivity of hybrids is due to heterojunction and (020) facets. • A possible photocatalytic degradation mechanism is proposed. - Abstract: Bi_2S_3/Bi_2WO_6 hybrid architectures with exposed (020) Bi_2WO_6 facets have been synthesized via a controlled anion exchange approach. X-ray photoelectron spectroscopy (XPS) reveals that a small amount of Bi_2S_3 was formed on the surface of Bi_2WO_6 during the anion exchange process, thus leading to the transformation from the Bi_2WO_6 to Bi_2S_3/Bi_2WO_6. A rhodamine B (RhB) aqueous solution was chosen as model organic pollutants to evaluate the photocatalytic activities of the Bi_2S_3/Bi_2WO_6 catalysts. Under visible light irradiation, the Bi_2S_3/Bi_2WO_6-TAA displayed the excellent visible light photoactivities compared with pure Bi_2S_3, Bi_2WO_6 and other composite photocatalysts. The efficient photocatalytic activity of the Bi_2S_3/Bi_2WO_6-TAA composite microspheres was ascribed to the constructed heterojunctions and the inner electric field caused by the exposed (020) Bi_2WO_6 facets. Active species trapping experiments revealed that h"+ and O_2·"− are the main active species in the photocatalytic process. Furthermore, the as-obtained photocatalysts showed good photocatalytic activity after four recycles. The results presented in this study provide a new concept for the rational design and development of highly efficient photocatalysts.

  14. Chimeric recombinant antibody fragments in cardiac troponin I immunoassay.

    Science.gov (United States)

    Hyytiä, Heidi; Heikkilä, Taina; Brockmann, Eeva-Christine; Kekki, Henna; Hedberg, Pirjo; Puolakanaho, Tarja; Lövgren, Timo; Pettersson, Kim

    2015-03-01

    To introduce a novel nanoparticle-based immunoassay for cardiac troponin I (cTnI) utilizing chimeric antibody fragments and to demonstrate that removal of antibody Fc-part and antibody chimerization decrease matrix related interferences. A sandwich-type immunoassay for cTnI based on recombinant chimeric (mouse variable/human constant) antigen binding (cFab) antibodies and intrinsically fluorescent nanoparticles was developed. To test whether using chimeric antibody fragments helps to avoid matrix related interferences, samples (n=39) with known amounts of triglycerides, bilirubin, rheumatoid factor (RF) or human anti-mouse antibodies (HAMAs) were measured with the novel assay, along with a previously published nanoparticle-based research assay with the same antibody epitopes. The limit of detection (LoD) was 3.30ng/L. Within-laboratory precision for 29ng/L and 2819ng/L cTnI were 13.7% and 15.9%, respectively. Regression analysis with Siemens ADVIA Centaur® yielded a slope (95% confidence intervals) of 0.18 (0.17-1.19) and a y-intercept of 1.94 (-1.28-3.91) ng/L. When compared to a previously published nanoparticle-based assay, the novel assay showed substantially reduced interference in the tested interference prone samples, 15.4 vs. 51.3%. A rheumatoid factor containing sample was decreased from 241ng/L to 3.3ng/L) immunoassay for the detection of cTnI and decreased matrix related interferences, thus resulting in a lower number of falsely elevated cTnI-values. Copyright © 2014 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.

  15. Structure of the short-range atomic order of WO3 amorphous films

    International Nuclear Information System (INIS)

    Olevskij, S.S.; Sergeev, M.S.; Tolstikhina, A.L.; Avilov, A.S.; Shkornyakov, S.M.; Semiletov, S.A.

    1984-01-01

    To study the causes of electrochromism manifestation in thin tungsten oxide films, the structure of WO 3 amorphous films has been investigated. The films were obtained by three different methods: by W(CO) 6 tungsten carbonyl pyrolysis, by high-frequency ion-plasma sputtering of a target prepared by WO 3 powder sintering, and by WO 3 powder thermal evaporation. Monocrystalline wafers of silicon and sodium chloride were used as substrates. The structure of short-range order in WO 3 amorphous films varies versus, the method of preparation in compliance with the type of polyhedral elements, (WO 6 , WO 5 ) and with the character of their packing (contacts via edges or vertices). Manifestation of electroc ro mism in WO 3 films prepared by varions methods and having different structure of short-range order is supposed to be realized through various mechanisms. One cannot exclude a potential simultaneous effect of the two coloration mechanisms

  16. Fabrication and photocatalytic activity enhanced mechanism of direct Z-scheme g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4} photocatalyst

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Bicheng [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Department of Science and Environmental Studies The Hong Kong Institute of Education, Tai Po, N.T., Hong Kong (China); Xia, Pengfei; Li, Yao [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Ho, Wingkei, E-mail: keithho@ied.edu.hk [Department of Science and Environmental Studies The Hong Kong Institute of Education, Tai Po, N.T., Hong Kong (China); Yu, Jiaguo, E-mail: jiaguoyu@yahoo.com [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah 21589 (Saudi Arabia)

    2017-01-01

    Highlights: • g-C{sub 3}N{sub 4} acted as a support for the in situ growth of β-Ag{sub 2}WO{sub 4}. • g-C{sub 3}N{sub 4} nanosheets inhibited the phase transformation of β-Ag{sub 2}WO{sub 4} to α-Ag{sub 2}WO{sub 4}. • g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4} exhibited a superior photocatalytic activity. • A direct Z-scheme photocatalytic mechanism could explain activity enhancement. - Abstract: Herein, a direct Z-scheme graphitic carbon nitride (g-C{sub 3}N{sub 4})/silver tungstate (Ag{sub 2}WO{sub 4}) photocatalyst was prepared by a facile in situ precipitation method using g-C{sub 3}N{sub 4} as a support and silver nitrate as a precursor. X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, and elemental mapping demonstrated that β-Ag{sub 2}WO{sub 4} nanoparticles were evenly distributed on the surface of g-C{sub 3}N{sub 4} nanosheets, which acted as a support for the nucleation and growth of β-Ag{sub 2}WO{sub 4} and inhibited the phase transformation of metastable β-Ag{sub 2}WO{sub 4} to stable α-Ag{sub 2}WO{sub 4}. Photocatalytic experiments indicated that the g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4} nanocomposite photocatalyst displayed a better photocatalytic activity than pure g-C{sub 3}N{sub 4} and Ag{sub 2}WO{sub 4} toward the degradation of methyl orange. The enhanced photocatalytic performance of g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4} could be well explained by a direct Z-scheme photocatalytic mechanism. This mechanism was related to the efficient space separation of photogenerated electron–hole pairs and the great oxidation and reduction capabilities of the g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4} system. This work provided new insights into the design and fabrication of g-C{sub 3}N{sub 4}-based direct Z-scheme photocatalysts.

  17. Structure and effects of silver nanoparticles on the surface of α-Ag{sub 2}-xWO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Gollino, Felipe; Silva, Alberico Borges Ferreira da, E-mail: felipe.gollino@gmail.com [Universidade de Sao Paulo (USP), Sao Carlos, SP (Brazil). Instituto de Quimica; Longo, Elson [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil)

    2016-07-01

    Full text: This work has the aim to study the effects of nanoparticles in the interface of microstructures of silver tungstate and silver tungstate with Ag nanoparticles trying to understand the influence of them in the material. The rods of α-Ag{sub 2}WO{sub 4} were synthesized using a microwave assisted hydrothermal (MAH) method, the samples was divided in two groups, the first one was irradiated by an electron beam, promoting the Ag{sup +} ions inside of the crystal to the surface of the material as nanoparticles of Ag{sup 0}, this growth could be accompanied in situ by MEV-FEG. The other one was submitted by a thermal treatment with intention to oxidize the surface of material. The materials were characterized structurally by Raman and infrared spectroscopies, which give the information on the atomic bonds, showing the same pattern. The phase of the material, the atomic positions and the structure distortions were confirmed by DRX pattern with Rietveld refinement. The electronic behavior was study by UV-Vis-NIR spectroscopy by determining the bandgap, and in the absorption measures, they were exhibited plasmon bands feature of metallic nanoparticles. In EFM images can be seen that the nanoparticles created does not present greater electric potential related by the matrix of Ag{sub 2}WO{sub 4}, what induces that each nanoparticle do not change their charge carriers with the crystal. The XPS measurements were performed to analyze the composition, and can be notice that the peaks had different shifts for the matrix and the nanoparticle, but in the thermally treated did not show that, this behavior could be interpreted by an independent behavior. (author)

  18. Hierarchical Bi{sub 2}WO{sub 6} architectures decorated with Pd nanoparticles for enhanced visible-light-driven photocatalytic activities

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jinniu; Chen, Tianhua [School of Physics and Information Technology, Shaanxi Normal University, Xi’an, 710062 (China); Lu, Hongbing, E-mail: hblu@snnu.edu.cn [School of Physics and Information Technology, Shaanxi Normal University, Xi’an, 710062 (China); Yang, Zhibo; Yin, Feng; Gao, Jianzhi; Liu, Qianru [School of Physics and Information Technology, Shaanxi Normal University, Xi’an, 710062 (China); Tu, Yafang [Department of Physics, Institute for Interdisciplinary Research, Jianghan University, Wuhan, 430056 (China)

    2017-05-15

    Highlights: • A new kind of Pd decorated Bi{sub 2}WO{sub 6} hierarchical microarchitecture was synthesized. • Pd nanoparticles remarkably improved the photocatalytic activity of Bi{sub 2}WO{sub 6}. • The photo-generated holes and ·O{sub 2}{sup −} played a crucial role in the degradation of RhB. • The photocatalytic enhancement mechanism of the Pd-Bi{sub 2}WO{sub 6} composites was proposed. - Abstract: A new kind of hierarchical Pd-Bi{sub 2}WO{sub 6} architecture decorated with different molar ratios of Pd to Bi, has been fabricated by a hydrothermal process, followed by a chemical deposition method. The photocatalytic activities of the pure Bi{sub 2}WO{sub 6} and Pd-Bi{sub 2}WO{sub 6} nanocatalyst were examined in the degradation of Rhodamine B (RhB) dyes and phenol under visible light. The photocatalytic results showed that the Pd-Bi{sub 2}WO{sub 6} nanocomposites possessed observably enhanced photocatalytic activities. Particularly, the 2.0% Pd loaded Bi{sub 2}WO{sub 6} had the highest photocatalytic activity, exhibiting a nearly complete degradation of 30 mg/L RhB and 10 mg/L phenol within only 50 and 60 min, respectively. In addition, the trapping experiment results indicated that the photo-generated holes (h{sup +}) and ·O{sub 2}{sup −} played a crucial role in the degradation of RhB. According to the experimental results, the photocatalytic degradation mechanism of Pd-Bi{sub 2}WO{sub 6} was also proposed. The enhanced photocatalytic activities were ascribed to the combined effects of the highly efficient separation of electrons and holes, improved visible light utilization and increased BET specific surface areas of the Pd-Bi{sub 2}WO{sub 6} nanocomposites.

  19. Characterization of nanoparticles of lidocaine in w/o microemulsions using small-angle neutron scattering and dynamic light scattering

    International Nuclear Information System (INIS)

    Shukla, A.; Kiselev, M.A.; Hoell, A.; Neubert, R.H.H.

    2004-01-01

    Microemulsions (MEs) are of special interest because a variety of reactants can be introduced into the nanometer-sized aqueous domains, leading to materials with controlled size and shape. In the past few years, significant research has been conducted in the reverse ME-mediated synthesis of organic nanoparticles. In this study, a w/o ME medium was employed for the synthesis of lidocaine by direct precipitation in w/o microemulsion systems: water/isopropylpalmitat/Tween80/Span80. The particle size as well as the location of nanoparticles in the ME droplet were characterized by means of dynamic light scattering (DLS) and small angle neutron scattering (SANS). It is observed that lidocaine precipitated in the aqueous cores because of its insolubility in water. Hydrodynamic radius and gyration radius of microemulsion droplets were estimated as ∼15 nm and ∼4.50 nm from DLS and SANS respectively. Furthermore, different size parameters obtained by DLS and SANS experiments were compared. (author)

  20. Facile synthesis of hierarchical double-shell WO{sub 3} microspheres with enhanced photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zhenfeng [College of Environment and Chemical Engineering, Tianjin Polytechnic University, Tianjin 300387 (China); State Key Laboratory of Hollow-Fiber Membrane Materials and Membrane Processes, Tianjin 300387 (China); Chu, Deqing, E-mail: dqingchu@163.com [College of Environment and Chemical Engineering, Tianjin Polytechnic University, Tianjin 300387 (China); State Key Laboratory of Hollow-Fiber Membrane Materials and Membrane Processes, Tianjin 300387 (China); Wang, Limin, E-mail: wanglimin@tjpu.edu.cn [School of Materials Science and Engineering, Tianjin Polytechnic University, Tianjin 300387 (China); State Key Laboratory of Hollow-Fiber Membrane Materials and Membrane Processes, Tianjin 300387 (China); Wang, Lipeng [School of Materials Science and Engineering, Tianjin Polytechnic University, Tianjin 300387 (China); Hu, Wenhui; Chen, Xiangyu; Yang, Huifang [College of Environment and Chemical Engineering, Tianjin Polytechnic University, Tianjin 300387 (China); Sun, Jingjing [School of Materials Science and Engineering, Tianjin Polytechnic University, Tianjin 300387 (China)

    2017-02-28

    Highlights: • HDS-WO{sub 3} were fabricated via mild process. • A possible growth mechanism for HDS-WO{sub 3} is proposed. • The excellent photocatalytic activity is attributed to the larger surface area of the HDS-WO{sub 3} nanostructures. - Abstract: Hierarchical double-shell WO{sub 3} microspheres (HDS-WO{sub 3}) have been successfully obtained through the thermal decomposition of WO{sub 3}·H{sub 2}O formed by metal salts as the templates. The products were characterized by X-ray diffraction (XRD), and the morphology was investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). In addition, the HDS-WO{sub 3} microspheres were analyzed by the Thermogravimetric (TG) and Brunauer-Emmett-Teller (BET) analysis. The synthetic mechanism of the products with hierarchical structures was proposed. The obtained HDS-WO{sub 3} exhibits excellent photocatalytic efficiency (84.9%), which is much higher than other WO{sub 3} sample under visible light illumination.

  1. Optical properties of WO3 thin films using surface plasmon resonance technique

    International Nuclear Information System (INIS)

    Paliwal, Ayushi; Sharma, Anjali; Gupta, Vinay; Tomar, Monika

    2014-01-01

    Indigenously assembled surface plasmon resonance (SPR) technique has been exploited to study the thickness dependent dielectric properties of WO 3 thin films. WO 3 thin films (80 nm to 200 nm) have been deposited onto gold (Au) coated glass prism by sputtering technique. The structural, optical properties and surface morphology of the deposited WO 3 thin films were studied using X-ray diffraction, UV-visible spectrophotometer, Raman spectroscopy, and Scanning electron microscopy (SEM). XRD analysis shows that all the deposited WO 3 thin films are exhibiting preferred (020) orientation and Raman data indicates that the films possess single phase monoclinic structure. SEM images reveal the variation in grain size with increase in thickness. The SPR reflectance curves of the WO 3 /Au/prism structure were utilized to estimate the dielectric properties of WO 3 thin films at optical frequency (λ = 633 nm). As the thickness of WO 3 thin film increases from 80 nm to 200 nm, the dielectric constant is seen to be decreasing from 5.76 to 3.42, while the dielectric loss reduces from 0.098 to 0.01. The estimated value of refractive index of WO 3 film is in agreement to that obtained from UV-visible spectroscopy studies. The strong dispersion in refractive index is observed with wavelength of incident laser light

  2. Biomimetic fabrication of WO3 for water splitting under visible light with high performance

    International Nuclear Information System (INIS)

    Yin, Chao; Zhu, Shenmin; Yao, Fan; Gu, Jiajun; Zhang, Wang; Chen, Zhixin; Zhang, Di

    2013-01-01

    Inspired by the high light-harvesting properties of typical butterfly wings, ceramic WO 3 butterfly wings with hierarchical structures of bio-butterfly wings was fabricated using a template of PapilioParis butterfly wings through a sol–gel method. The effect of calcination temperatures on the structures of the ceramic butterfly wings was investigated and the results showed that the WO 3 butterfly wing replica calcined at 550 °C (WO 3 replica-550) is a single phase and has a high crystallinity and relatively fine hierarchical structure. The average grain size of WO 3 replica-550 and WO 3 powder are around 32.6 and 42.2 nm, respectively. Compared with pure WO 3 powder, WO 3 replica-550 demonstrated a higher light-harvesting capability in the region from 460 to 700 nm and more importantly the higher charge separation rate, as evidenced by electron paramagnetic resonance measurements. Photocatalytic O 2 evolutions from water were investigated on the ceramic butterfly wings and pure WO 3 powder under visible light (λ > 420 nm). The results showed that the amount of O 2 produced from WO 3 replica-550 is 50 % higher than that of the pure WO 3 powder. The improved photocatalytic performance of WO 3 replica-550 is attributed to the quasi-honeycomb structure inherited from the PapilioParis butterfly wings, providing both high light-harvesting efficiency and efficient charge transport through the WO 3

  3. Preparation and characterization of nanocrystalline porous TiO2/WO3 composite thin films

    International Nuclear Information System (INIS)

    Hsu, C.-S.; Lin, C.-K.; Chan, C.-C.; Chang, C.-C.; Tsay, C.-Y.

    2006-01-01

    TiO 2 materials possessing not only photocatalytic but also electrochromic properties have attracted many research and development interests. Though WO 3 exhibits excellent electrochromic properties, the much higher cost and water-sensitivity of WO 3 as compared with the TiO 2 may restrict the practical application of WO 3 materials. In the present study, the feasibility of preparing nanocrystalline porous TiO 2 /WO 3 composite thin films was investigated. Precursors of sols TiO 2 and/or WO 3 and polystyrene microspheres were used to prepare nanocrystalline pure TiO 2 , WO 3 , and composite TiO 2 /WO 3 thin films by spin coating. The spin-coated thin films were amorphous and, after heat treating at a temperature of 500 o C, nanocrystalline TiO 2 , TiO 2 /WO 3 , and WO 3 thin films with or without pores were prepared successfully. The heat-treated thin films were colorless and coloration-bleaching phenomena can be observed during cyclic voltammetry tests. The heat-treated thin films exhibited good reversible electrochromic behavior while the porous TiO 2 /WO 3 composite film exhibited improved electrochromic properties

  4. Photocatalytic reduction of CO{sub 2} into methanol and ethanol over conducting polymers modified Bi{sub 2}WO{sub 6} microspheres under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Dai, Weili, E-mail: wldai81@126.com; Xu, Hai; Yu, Juanjuan; Hu, Xu; Luo, Xubiao, E-mail: luoxubiao@126.com; Tu, Xinman; Yang, Lixia

    2015-11-30

    Graphical abstract: - Highlights: • Conducting polymers modified Bi{sub 2}WO{sub 6} HHMS (CP/Bi{sub 2}WO{sub 6}) was successfully synthesized. • The introduction of CP decreases the recombination of photogenerated e{sup –}–h{sup +} pairs. • The PTh/Bi{sub 2}WO{sub 6} exhibites good stability and recyclability for CO{sub 2} photoreduction. • The possible photocatalytic mechanism was discussed and proposed. - Abstract: Bi{sub 2}WO{sub 6} hierarchical hollow microspheres (HHMS) modified with different conducting polymers (polyaniline, polypyrrole, and polythiophene) were successfully synthesized by ‘in situ’ deposition oxidative polymerization method, and evaluated as photocatalysts for the photocatalytic reduction of CO{sub 2} with H{sub 2}O to methanol and ethanol. It was found that the introduction of conducting polymers obviously decreased the recombination of photogenerated electron–hole pairs, thus promoting the photocatalytic activity of Bi{sub 2}WO{sub 6}. Among the as-fabricated photocatalysts, polythiophene modified Bi{sub 2}WO{sub 6} (PTh/Bi{sub 2}WO{sub 6}) exhibited the best photoelectronic and photocatalytic performance, due to the narrow band gap and good charge mobility of polythiophene. The results demonstrate that the methanol and ethanol yield over PTh/Bi{sub 2}WO{sub 6} was 56.5 and 20.5 μmol g{sub cat}{sup −1} in 4 h, respectively. The total yield of hydrocarbons is 2.8 times higher than that over pure Bi{sub 2}WO{sub 6}. It is noted that the catalyst exhibits good recyclability and stability. After five consecutive runs, the PTh/Bi{sub 2}WO{sub 6} catalyst shows no significant loss of photocatalytic activity. The possible photocatalytic mechanism was proposed which is beneficial for further improving the activity of photocatalysts. The approach described in this study provides a simple and reliable strategy for the rational design of efficient visible light-driven photocatalysts for photoreduction of CO{sub 2} to hydrocarbons.

  5. Characterization of MAPLE deposited WO3 thin films for electrochromic applications

    Science.gov (United States)

    Boyadjiev, S. I.; Stefan, N.; Szilágyi, I. M.; Mihailescu, N.; Visan, A.; Mihailescu, I. N.; Stan, G. E.; Besleaga, C.; Iliev, M. T.; Gesheva, K. A.

    2017-01-01

    Tungsten trioxide (WO3) is a widely studied material for electrochromic applications. The structure, morphology and optical properties of WO3 thin films, grown by matrix assisted pulsed laser evaporation (MAPLE) from monoclinic WO3 nano-sized particles, were investigated for their possible application as electrochromic layers. A KrF* excimer (λ=248 nm, ζFWHM=25 ns) laser source was used in all experiments. The MAPLE deposited WO3 thin films were studied by atomic force microscopy (AFM), grazing incidence X-ray diffraction (GIXRD) and Fourier transform infrared spectroscopy (FTIR). Cyclic voltammetry measurements were also performed, and the coloring and bleaching were observed. The morpho-structural investigations disclosed the synthesis of single-phase monoclinic WO3 films consisting of crystalline nano-grains embedded in an amorphous matrix. All thin films showed good electrochromic properties, thus validating application of the MAPLE deposition technique for the further development of electrochromic devices.

  6. Characterization of MAPLE deposited WO3 thin films for electrochromic applications

    International Nuclear Information System (INIS)

    Boyadjiev, S I; Iliev, M T; Stefan, N; Mihailescu, N; Visan, A; Mihailescu, I N; Szilágyi, I M; Stan, G E; Besleaga, C; Gesheva, K A

    2017-01-01

    Tungsten trioxide (WO 3 ) is a widely studied material for electrochromic applications. The structure, morphology and optical properties of WO 3 thin films, grown by matrix assisted pulsed laser evaporation (MAPLE) from monoclinic WO 3 nano-sized particles, were investigated for their possible application as electrochromic layers. A KrF* excimer (λ=248 nm, ζ FWHM =25 ns) laser source was used in all experiments. The MAPLE deposited WO 3 thin films were studied by atomic force microscopy (AFM), grazing incidence X-ray diffraction (GIXRD) and Fourier transform infrared spectroscopy (FTIR). Cyclic voltammetry measurements were also performed, and the coloring and bleaching were observed. The morpho-structural investigations disclosed the synthesis of single-phase monoclinic WO 3 films consisting of crystalline nano-grains embedded in an amorphous matrix. All thin films showed good electrochromic properties, thus validating application of the MAPLE deposition technique for the further development of electrochromic devices. (paper)

  7. Preparation of WO{sub 3}/g-C{sub 3}N{sub 4} composites and their application in oxidative desulfurization

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Rongxiang, E-mail: zylhzrx@126.com; Li, Xiuping, E-mail: lilili_171717@126.com; Su, Jianxun; Gao, Xiaohan

    2017-01-15

    Highlights: • The WO{sub 3}/g-C{sub 3}N{sub 4} was successfully synthesized through simple calcination. • The process is simple and the cost raw materials is cheap. • The WO{sub 3}/g-C{sub 3}N{sub 4} firstly applied to ODS. • The desulpurization rate of WO{sub 3}/g-C{sub 3}N{sub 4} may attach to 91.2%. • Five recycles of WO{sub 3}/g-C{sub 3}N{sub 4} still attach to 89.5% due to heterogeneous catalysis. - Abstract: WO{sub 3}/graphitic carbon nitride (g-C{sub 3}N{sub 4}) composites were successfully synthesized through direct calcining of a mixture of WO{sub 3} and g-C{sub 3}N{sub 4} at 400 °C for 2 h. The WO{sub 3} was prepared by calcination of phosphotungstic acid at 550 °C for 4 h, and the g-C{sub 3}N{sub 4} was obtained by calcination of melamine at 520 °C for 4 h. The WO{sub 3}/g-C{sub 3}N{sub 4} composites were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), and Brunner−Emmett−Teller analysis (BET). The WO{sub 3}/g-C{sub 3}N{sub 4} composites exhibited stronger XRD peaks of WO{sub 3} and g-C{sub 3}N{sub 4} than the WO{sub 3} and pure g-C{sub 3}N{sub 4}. In addition, two WO{sub 3} peaks at 25.7° and 26.6° emerged for the 36% −WO{sub 3}/g-C{sub 3}N{sub 4} composite. This finding indicated that WO{sub 3} was highly dispersed on the surface of the g-C{sub 3}N{sub 4} nanosheets and interacted with the nanosheets, which resulted in the appearance of (012) and (022) planes of WO{sub 3}. The WO{sub 3}/g-C{sub 3}N{sub 4} composite also exhibited a larger specific surface area and higher degree of crystallization than WO{sub 3} or pure g-C{sub 3}N{sub 4}, which resulted in high catalytic activity of the catalyst. Desulfurization experiments demonstrated that the desulfurization rate of dibenzothiophene (DBT) in model oil reached 91.2% under optimal conditions. Moreover, the activity of the catalyst was not significantly decreased after five recycles.

  8. An Ultrasensitive Electrochemiluminescence Immunoassay for Carbohydrate Antigen 19-9 in Serum Based on Antibody Labeled Fe3O4 Nanoparticles as Capture Probes and Graphene/CdTe Quantum Dot Bionanoconjugates as Signal Amplifiers

    Science.gov (United States)

    Gan, Ning; Zhou, Jing; Xiong, Ping; Li, Tianhua; Jiang, Shan; Cao, Yuting; Jiang, Qianli

    2013-01-01

    The CdTe quantum dots (QDs), graphene nanocomposite (CdTe-G) and dextran–Fe3O4 magnetic nanoparticles have been synthesized for developing an ultrasensitive electrochemiluminescence (ECL) immunoassay for Carcinoembryonic antigen 19-9 (CA 19-9) in serums. Firstly, the capture probes (CA 19-9 Ab1/Fe3O4) for enriching CA 19-9 were synthesized by immobilizing the CA 19-9’s first antibody (CA 19-9 Ab1) on magnetic nanoparticles (dextran-Fe3O4). Secondly, the signal probes (CA 19-9 Ab2/CdTe-G), which can emit an ECL signal, were formed by attaching the secondary CA 19-9 antibody (CA 19-9 Ab2) to the surface of the CdTe-G. Thirdly, the above two probes were used for conjugating with a serial of CA 19-9 concentrations. Graphene can immobilize dozens of CdTe QDs on their surface, which can emit stronger ECL intensity than CdTe QDs. Based on the amplified signal, ultrasensitive antigen detection can be realized. Under the optimal conditions, the ECL signal depended linearly on the logarithm of CA 19-9 concentration from 0.005 to 100 pg/mL, and the detection limit was 0.002 pg/mL. Finally, five samples of human serum were tested, and the results were compared with a time-resolved fluorescence assay (TRFA). The novel immunoassay provides a stable, specific and highly sensitive immunoassay protocol for tumor marker detection at very low levels, which can be applied in early diagnosis of tumor. PMID:23685872

  9. Structural and optical properties of crystalline and nanocrystalline NaIn(WO4)2:Cr3+

    International Nuclear Information System (INIS)

    Fuks, H.; Skibiński, T.; Kaczmarek, S.M.; Hanuza, J.; Leniec, G.; Hermanowicz, K.; Mączka, M.; Ptak, M.

    2014-01-01

    Highlights: • Optical properties are summarized for single crystals and nanopowders of NaIn(WO 4 ) 2 :Cr. • EPR properties are compared in terms of different site occupation of Cr ion in the NaIn(WO 4 ) 2 matrix. • The changes in the PL and ESR properties of the nanopowders vs. their decreasing size are studied. • An increase of isolated ions with temperature at the expense of chromium complexes is observed. • Magnetic susceptibility and moment of the powders are discussed in terms of Cr substitution. -- Abstract: EPR and optical spectra of chromium doped NaIn(WO 4 ) 2 single crystals and nanopowders have been measured. The resonance EPR measurements have been performed for two crystal orientations in respect to the magnetic field and analyzed in terms of various Cr 3+ ion site occupancies in the crystal lattice. They have been structurally and optically identified. The changes in the photoluminescence and electron spin resonance properties of the nanoparticles vs. their decreasing size have also been studied. Magnetic susceptibility and effective magnetic moment of the nanopowders were measured and discussed in terms of chromium substitution. Comparisons between chromium substitution in single crystals and nanopowders have been performed

  10. Synthesis of WO3 flower-like hierarchical architectures and their sensing properties

    International Nuclear Information System (INIS)

    Meng, Dan; Wang, Guosheng; San, Xiaoguang; Song, Yinmin; Shen, Yanbai; Zhang, Yajing; Wang, Kangjun; Meng, Fanli

    2015-01-01

    WO 3 flower-like hierarchical architectures were synthesized by hydrothermal process using sodium tungstate (Na 2 WO 4 ·2H 2 O) as tungsten source and citric acid (CA) as an assistant agent. The morphology and crystal structure were investigated using scanning electron microscope and X-ray diffractometer. It is found that CA played a significant role in governing morphologies of product during hydrothermal process. The obtained products were identified as triclinic crystal WO 3 structure. The ethanol gas sensing measurements showed that well-defined WO 3 flower-like structures synthesized at CA/W molar ratio of 1 with large specific surface area exhibited the higher responses compared with others at all operating temperatures. Moreover, the reversible and fast response to ethanol gas at various gas concentrations and good selectivity were obtained. The results indicated that the WO 3 flower-like hierarchical architectures are promising materials for gas sensors. - Highlights: • WO 3 flower-like structures were successfully synthesized by hydrothermal method. • The effect of citric acid amount on morphologies was investigated. • Good ethanol gas sensing properties of WO 3 flower-like structures were obtained

  11. Influence of disordered morphology on electrochromic stability of WO{sub 3}/PPy

    Energy Technology Data Exchange (ETDEWEB)

    Gaikwad, Digambar K. [D. Y. Patil College of Engineering & Technology, Kasaba Bawada, Kolhapur, 416006, Maharashtra (India); Mali, Sawanta S.; Hong, Chang K. [Polymer Energy Materials Laboratory, Department of Advanced Chemical Engineering, Chonnam National University, Gwangju, 500-757 (Korea, Republic of); Kadam, Anamika V., E-mail: anamikasonavane@rediff.com [D. Y. Patil College of Engineering & Technology, Kasaba Bawada, Kolhapur, 416006, Maharashtra (India); D.Y. Patil Medical University, Kasaba Bawada, Kolhapur, 416006, Maharashtra (India)

    2016-06-05

    Tungsten oxide (WO{sub 3}) films are critical for smart windows because of their capacity of varying the throughput of visible light and solar energy. This study highlights the evolution of structural and morphological changes of electrodeposited WO{sub 3} thin films coated with polypyrrole (PPy) by using chemical bath deposition. The structural and surface properties of WO{sub 3} thin films were studied using X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and transmission electron microscopy. The electrochemical stability was inspected using repetitive cyclic voltammetry (CV) cycles for each sample in LiClO{sub 4}-PC electrolyte for prolonged periods. The results showed an improvement in the electrochemical stability after the CV study. - Graphical abstract: Mechanism: A schematic of the mechanism is proposed in above fig. The mechanism is based on three step process: (i) WO{sub 3} coated on ITO by electrodeposition followed by thermal treatment. It produces ordered nanoarrayed morphology. (ii) A second step involving deposition of PPy by chemical bath deposition on ITO. It possesses globular morphology. (iii) When PPy coated on WO{sub 3}, PPy applies shearing force on WO{sub 3} and produces disordered nanoarrayed morphology. - Highlights: • Nanoarrayed WO{sub 3}/PPy composite was synthesized. • Interplanar spacing enhances due to PPy coating. • PPy applies shearing force on WO{sub 3} produces disordered morphology. • Nanocomposite showed high stability in LiClO{sub 4}-PC.

  12. Review of WO3 thin film preparation for photoelectrochemical water splitting

    International Nuclear Information System (INIS)

    Ehsan Eftekhari; Mohammad Kassim

    2009-01-01

    Full text: Tungsten trioxide (WO 3 ), which is one of the most essential materials in our daily life has appeared as an excellent photo electrode material for environmental purification. The nano-size of WO 3 thin film water-splitting technology has great potential for environmentally friendly solar-hydrogen production for the future hydrogen economy. There are several methods for producing tungsten oxide film. In this review, we outlined several WO 3 thin film preparation methods such as doctor Bladding, sputtering, layer-by-layer brush painting, spray pyrolysis deposition, sol-gel and other methods. Here we compare the maximum photocurrent obtained, different condition for preparation of WO 3 thin film and characterization outcome. (author)

  13. Gas-sensing properties of In{sub 2}O{sub 3} films modified with gold nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Korotcenkov, G., E-mail: ghkoro@yahoo.com [School of Material Science and Engineering, Gwangju Institute of Science and Technology, Gwangju (Korea, Republic of); Brinzari, V. [Department of Theoretical Physics, State University of Moldova, Chisinau, Republic of Moldova (Moldova, Republic of); Han, S.H. [Division of Maritime Transportation System, Mokpo National Maritime University, Mokpo (Korea, Republic of); Cho, B.K., E-mail: chobk@gist.ac.kr [School of Material Science and Engineering, Gwangju Institute of Science and Technology, Gwangju (Korea, Republic of)

    2016-06-01

    A study of the surface and gas–sensitive properties of In{sub 2}O{sub 3} films modified with gold nanoparticles and synthesized by the successive ionic layer deposition (SILD) method was conducted. In{sub 2}O{sub 3} films were prepared using the spray pyrolysis method. The gas-sensing characteristics were tested using CO, H{sub 2}, and O{sub 3} as target gases. It has been shown that the surface modification with gold nanoparticles gives the opportunity to optimize the response of In{sub 2}O{sub 3}-based gas sensors to both reducing (CO, H{sub 2}) and oxidizing (O{sub 3}) gases. It has been found that the sensitizing effect during ozone detection was significantly higher than the effect during CO and H{sub 2} detection. It has been demonstrated that the sensitizing effect depended on the number of SILD cycles used for gold nanoparticle deposition and was maximal for the In{sub 2}O{sub 3} surface decorated with gold nanoparticles with the smallest size. The mechanism of the gold nanoparticles' influence on the gas-sensing properties of the In{sub 2}O{sub 3} films is also discussed. It is suggested that to explain the observed effects, we have to consider both the “electronic” and “chemical” mechanisms of sensitization. Suggestions for studies to be carried out to further improve both the understanding of the nature of the gas-sensitive effects and the parameters of In{sub 2}O{sub 3}:Au-based gas sensors are also formulated. - Highlights: • In{sub 2}O{sub 3} gas sensors modified with gold nanoparticles using SILD method are studied. • AuNPs exhibit activity during interaction with either reducing or oxidizing gases. • Maximal effect of optimization is observed during ozone detection. • Sensitizing effect depends on the number of SILD cycles. • Proposed mechanisms explain effects observed in the In{sub 2}O{sub 3}:Au based gas sensors.

  14. Tungsten oxide (WO3) thin films for application in advanced energy systems

    International Nuclear Information System (INIS)

    Gullapalli, S. K.; Vemuri, R. S.; Manciu, F. S.; Enriquez, J. L.; Ramana, C. V.

    2010-01-01

    Inherent processes in coal gasification plants produce hazardous hydrogen sulfide (H 2 S), which must be continuously and efficiently detected and removed before the fuel is used for power generation. An attempt has been made in this work to fabricate tungsten oxide (WO 3 ) thin films by radio-frequency reactive magnetron-sputter deposition. The impetus being the use of WO 3 films for H 2 S sensors in coal gasification plants. The effect of growth temperature, which is varied in the range of 30-500 deg. C, on the growth and microstructure of WO 3 thin films is investigated. Characterizations made using scanning electron microscopy (SEM) and x-ray diffraction (XRD) indicate that the effect of temperature is significant on the microstructure of WO 3 films. XRD and SEM results indicate that the WO 3 films grown at room temperature are amorphous, whereas films grown at higher temperatures are nanocrystalline. The average grain-size increases with increasing temperature. WO 3 films exhibit smooth morphology at growth temperatures ≤300 deg. C while relatively rough at >300 deg. C. The analyses indicate that the nanocrystalline WO 3 films grown at 100-300 deg. C could be the potential candidates for H 2 S sensor development for application in coal gasification systems.

  15. Horseradish peroxidase-loaded nanospheres attached to hollow gold nanoparticles as signal enhancers in an ultrasensitive immunoassay for alpha-fetoprotein

    International Nuclear Information System (INIS)

    Li, Ya; Yuan, Ruo; Chai, Yaqin; Zhuo, Ying; Su, Huilan; Zhang, Yuxia

    2014-01-01

    We report on a novel electrochemical signal amplification strategy for use in immunoassays. The highly responsive immunoelectrode was constructed in the following way: (1) The surface of a gold electrode was covered with a layer single-walled carbon nanotubes dispersed in chitosane functionalized with L-cysteine; (2) Gold nanoparticles containing protein A and anti-alpha-fetoprotein (anti-AFP) were then covalently attached to the surface via the thiol groups of the chitosane. The electrode is then exposed to the analyte (AFP) which then is bound by the antibody. In the next step, a gold-conjugated secondary antibody is added that was prepared in the following way: (1) Horseradish peroxidase was crosslinked and the resulting spheres were coated with hollow gold nanoparticles (hollow Au-NPs) to give nanospheres of ∼100 nm in diameter. (2) These were the coated with thionine and, in a last step, with secondary antibody. The use of these materials has several attractive features: The HRP-NPs functionalized with hollow Au-NPs possess a large surface area that can load the large amount of secondary antibody. Thionine (Thi) is highly redox active and improves the intensity of the signal. Carbon nanotubes were used because they possess an excellent electron transfer rate and large surface area. Following incubation of the modified electrode (a) with a sample containing AFP, (b) then with the secondary antibody, and (c) with washing buffer, the electrode is placed in a solution containing H 2 O 2 . The HRP in the smart secondary antibody causes the catalytic decomposition of H 2 O 2 and the results in an electrical current that is linearly related to the concentration of AFP in the 0.025 to 5.0 ng mL −1 concentration range. The detection limit for AFP is as low as 8.3 pg mL −1 . We believe that this novel kind of immunoassay represents a promising tool for use in sensitive clinical assays. (author)

  16. Super-Nernstian pH sensors based on WO3 nanosheets

    Science.gov (United States)

    Kuo, Chao-Yin; Wang, Shui-Jinn; Ko, Rong-Ming; Tseng, Hung-Hao

    2018-04-01

    The effects of the surface morphology of hydrothermally grown WO3 nanosheets (NSs) and sputtering WO3 film on the performance of pH sensing electrodes are presented and compared in the pH range of 2–12. Using a separated electrode of an extended-gate field-effect transistor (EGFET) configuration, the WO3 nanosheet (NS) pH sensor shows a sensitivity of 63.37 mV/pH, a good linearity of 0.9973, a low voltage hysteresis of 4.79 mV, and a low drift rate of 3.18 mV/h. In contrast, the film-type one shows a typical sensitivity of only 50.08 mV/pH and a linearity of 0.9932. The super-Nernstian response could be attributed to the significant increase in the number of surface ion adsorption sites of the NS structure and the occurrence of local electric field enhancement over the sharp edges and corners of WO3 NSs.

  17. Exploration on anion ordering, optical properties and electronic structure in K{sub 3}WO{sub 3}F{sub 3} elpasolite

    Energy Technology Data Exchange (ETDEWEB)

    Atuchin, V.V. [Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090 (Russian Federation); Isaenko, L.I. [Laboratory of Crystal Growth, Institute of Geology and Mineralogy, SB RAS, Novosibirsk 630090 (Russian Federation); Kesler, V.G. [Laboratory of Physical Principles for Integrated Microelectronics, Institute of Semiconductor Physics, Novosibirsk 630090 (Russian Federation); Lin, Z.S., E-mail: zslin@mail.ipc.ac.cn [Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, P.O. Box 2711, Beijing 100190 (China); Molokeev, M.S. [Laboratory of Crystal Physics, Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Yelisseyev, A.P.; Zhurkov, S.A. [Laboratory of Crystal Growth, Institute of Geology and Mineralogy, SB RAS, Novosibirsk 630090 (Russian Federation)

    2012-03-15

    Room-temperature modification of potassium oxyfluorotungstate, G2-K{sub 3}WO{sub 3}F{sub 3}, has been prepared by low-temperature chemical route and single crystal growth. Wide optical transparency range of 0.3-9.4 {mu}m and forbidden band gap E{sub g}=4.32 eV have been obtained for G2-K{sub 3}WO{sub 3}F{sub 3} crystal. Meanwhile, its electronic structure has been calculated with the first-principles calculations. The good agreement between the theorectical and experimental results have been achieved. Furthermore, G2-K{sub 3}WO{sub 3}F{sub 3} is predicted to possess the relatively large nonlinear optical coefficients. - Graphical abstract: Using the cm-size K{sub 3}WO{sub 3}F{sub 3} crystal (left upper), the transmission spectrum (right upper) and XPS valence electronic states (left lower) were measured, agreed with the ab initio results (right lower). Highlights: Black-Right-Pointing-Pointer The cm-size G2-K{sub 3}WO{sub 3}F{sub 3} single crystals are obtained. Black-Right-Pointing-Pointer Optical absorption edge and transmission range are defined for G2-K{sub 3}WO{sub 3}F{sub 3} crystal. Black-Right-Pointing-Pointer Crystal structures of all known K{sub 3}WO{sub 3}F{sub 3} polymorph modifications are determined. Black-Right-Pointing-Pointer Experimental electronic structure is consistent with the first-principles result. Black-Right-Pointing-Pointer G2-K{sub 3}WO{sub 3}F{sub 3} is predicted as a crystal with large NLO coefficients.

  18. Gas sensing properties of graphene–WO3 composites prepared by hydrothermal method

    International Nuclear Information System (INIS)

    Chu, Xiangfeng; Hu, Tao; Gao, Feng; Dong, Yongping; Sun, Wenqi; Bai, Linshan

    2015-01-01

    Graphical abstract: - Highlights: • The amount of graphene had an effect on the morphology of graphene–WO 3 composites. • The optimum temperature of 0.1 wt% graphene–WO 3 sensor to acetaldehyde was 100 °C. • 0.1 wt% graphene–WO 3 sensor exhibited good selectivity to acetaldehyde at 100 °C. - Abstract: Graphene–WO 3 composites mixed with different amounts of graphene (0, 0.1, 0.5, 1 and 3 wt%) were prepared by hydrothermal method at 180 °C for 24 h. The as-prepared graphite oxide, graphene and graphene–WO 3 composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectra (FT-IR) and Raman spectroscopy, respectively. The effect of the amount of graphene in the composites on the gas-sensing responses and the gas-sensing selectivity of the materials was investigated. The experimental results revealed that the sensor based on 0.1 wt% graphene–WO 3 composite exhibited high response and good selectivity to acetaldehyde vapor at 100 °C, the optimum operating temperature of this sensor to 1000 ppm acetaldehyde vapor decreased from 180 °C to 100 °C comparing with that of pure WO 3 . The response time and the recovery time for 100 ppm acetaldehyde vapor were 250 s and 225 s, respectively

  19. Synthesis of tungsten oxide nanoparticles using a hydrothermal method at ambient pressure

    DEFF Research Database (Denmark)

    Ahmadi, Majid; Younesi, Reza; Guinel, Maxime J-F

    2014-01-01

    ) nanoparticles were synthesized using a simple and inexpensive low temperature and low pressure hydrothermal (HT) method. The precursor solution used for the HT process was prepared by adding hydrochloric acid to diluted sodium tungstate solutions (Na2WO4 center dot 2H(2)O) at temperatures below 5 degrees C...... and then dissolved using oxalic acid. This HT process yielded tungstite (WO3 center dot H2O) nanoparticles with the orthorhombic structure. A heat treatment at temperatures at or above 300 degrees C resulted in a phase transformation to monoclinic WO3, while preserving the nanoparticles morphology. The production...

  20. Optimization, Yield Studies and Morphology of WO3Nano-Wires Synthesized by Laser Pyrolysis in C2H2and O2Ambients—Validation of a New Growth Mechanism

    Directory of Open Access Journals (Sweden)

    Sideras-Haddad E

    2008-01-01

    Full Text Available Abstract Laser pyrolysis has been used to synthesize WO3nanostructures. Spherical nano-particles were obtained when acetylene was used to carry the precursor droplet, whereas thin films were obtained at high flow-rates of oxygen carrier gas. In both environments WO3nano-wires appear only after thermal annealing of the as-deposited powders and films. Samples produced under oxygen carrier gas in the laser pyrolysis system gave a higher yield of WO3nano-wires after annealing than the samples which were run under acetylene carrier gas. Alongside the targeted nano-wires, the acetylene-ran samples showed trace amounts of multi-walled carbon nano-tubes; such carbon nano-tubes are not seen in the oxygen-processed WO3nano-wires. The solid–vapour–solid (SVS mechanism [B. Mwakikunga et al., J. Nanosci. Nanotechnol., 2008] was found to be the possible mechanism that explains the manner of growth of the nano-wires. This model, based on the theory from basic statistical mechanics has herein been validated by length-diameter data for the produced WO3nano-wires.

  1. Preparation, characterization of Fe3O4 at TiO2 magnetic nanoparticles and their application for immunoassay of biomarker of exposure to organophosphorus pesticides

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Xiao; Wang, Hongbo; Yang, Chunming; Du, Dan; Lin, Yuehe

    2013-03-15

    Novel Fe3O4 at TiO2 magnetic nanoparticles were prepared and developed for a new nanoparticle-based immunosensor for electrochemical quantification of organophosphorylated butyrylcholinesterase (BChE) in plasma, a specific biomarker of exposure to organophosphorus (OP) agents. The Fe3O4 at TiO2 nanoparticles were synthesized by hydrolysis of tetrabutyltitanate on the surface of Fe3O4 magnetic nanospheres, and characterized by attenuated total reflection Fourier-transform infrared spectra, transmission electron microscope and X-ray diffraction. The functional Fe3O4 at TiO2 nanoparticles were performed as capture antibody to selectively enrich phosphorylated moiety instead of phosphoserine antibody in the traditional sandwich immunoassays. The secondary recognition was served by quantum dots (QDs)-tagged anti-BChE antibody (QDs-anti-BChE). With the help of a magnet, the resulting sandwich-like complex, Fe3O4 at TiO2/OP-BChE/QDs-anti-BChE, was easily isolated from sample solutions and the released cadmium ions were detected on a disposable screen-printed electrode (SPE). The binding affinities were investigated by both surface plasmon resonance (SPR) and square wave voltammetry (SWV). This method not only avoids the drawback of unavailability of commercial OP-specific antibody but also amplifies detection signal by QDs-tags together with easy separation of samples by magnetic forces. The proposed immunosensor yields a linear response over a broad OP-BChE concentrations range from 0.02 to 10 nM, with detection limit of 0.01 nM. Moreover, the disposable nanoparticle-based immunosensor has been validated with human plasma samples. It offers a new method for rapid, sensitive, selective and inexpensive screening/evaluating exposure to OP pesticides.

  2. Actively-targeted LTVSPWY peptide-modified magnetic nanoparticles for tumor imaging

    Directory of Open Access Journals (Sweden)

    Jie L-Y

    2012-07-01

    Full Text Available Li-Yong Jie,1 Li-Li Cai,2 Le-Jian Wang,2 Xiao-Ying Ying,2 Ri-Sheng Yu,1 Min-Ming Zhang,1 Yong-Zhong Du21Department of Radiology, The Second Affiliated Hospital, Zhejiang University School of Medicine, 2College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, People's Republic of ChinaBackground: Magnetic resonance imaging (MRI is widely used in modern clinical medicine as a diagnostic tool, and provides noninvasive and three-dimensional visualization of biological phenomena in living organisms with high spatial and temporal resolution. Therefore, considerable attention has been paid to magnetic nanoparticles as MRI contrast agents with efficient targeting ability and cellular internalization ability, which make it possible to offer higher contrast and information-rich images for detection of disease.Methods: LTVSPWY peptide-modified PEGylated chitosan (LTVSPWY-PEG-CS was synthesized by chemical reaction, and the chemical structure was confirmed by 1H-NMR. LTVSPWY-PEG-CS-modified magnetic nanoparticles were prepared successfully using the solvent diffusion method. Their particle size, size distribution, and zeta potential were measured by dynamic light scattering and electrophoretic mobility, and their surface morphology was investigated by transmission electron microscopy. To investigate their selective targeting ability, the cellular uptake of the LTVSPWY-PEG-CS-modified magnetic nanoparticles was observed in a cocultured system of SKOV-3 cells which overexpress HER2 and A549 cells which are HER2-negative. The in vitro cytotoxicity of these nanoparticles in SKOV-3 and A549 cells was measured using the MTT method. The SKOV-3-bearing nude mouse model was used to investigate the tumor targeting ability of the magnetic nanoparticles in vivo.Results: The average diameter and zeta potential of the LTVSPWY-PEG-CS-modified magnetic nanoparticles was 267.3 ± 23.4 nm and 30.5 ± 7.0 mV, respectively, with a narrow size distribution and

  3. Optical properties of WO{sub 3} thin films using surface plasmon resonance technique

    Energy Technology Data Exchange (ETDEWEB)

    Paliwal, Ayushi; Sharma, Anjali; Gupta, Vinay, E-mail: drguptavinay@gmail.com, E-mail: vgupta@physics.du.ac.in [Department of Physics and Astrophysics, University of Delhi, Delhi 110007 (India); Tomar, Monika [Department of Physics, Miranda House, University of Delhi, Delhi 110007 (India)

    2014-01-28

    Indigenously assembled surface plasmon resonance (SPR) technique has been exploited to study the thickness dependent dielectric properties of WO{sub 3} thin films. WO{sub 3} thin films (80 nm to 200 nm) have been deposited onto gold (Au) coated glass prism by sputtering technique. The structural, optical properties and surface morphology of the deposited WO{sub 3} thin films were studied using X-ray diffraction, UV-visible spectrophotometer, Raman spectroscopy, and Scanning electron microscopy (SEM). XRD analysis shows that all the deposited WO{sub 3} thin films are exhibiting preferred (020) orientation and Raman data indicates that the films possess single phase monoclinic structure. SEM images reveal the variation in grain size with increase in thickness. The SPR reflectance curves of the WO{sub 3}/Au/prism structure were utilized to estimate the dielectric properties of WO{sub 3} thin films at optical frequency (λ = 633 nm). As the thickness of WO{sub 3} thin film increases from 80 nm to 200 nm, the dielectric constant is seen to be decreasing from 5.76 to 3.42, while the dielectric loss reduces from 0.098 to 0.01. The estimated value of refractive index of WO{sub 3} film is in agreement to that obtained from UV-visible spectroscopy studies. The strong dispersion in refractive index is observed with wavelength of incident laser light.

  4. Photoelectrochemical sensitive detection of insulin based on CdS/polydopamine co-sensitized WO3 nanorod and signal amplification of carbon nanotubes@polydopamine.

    Science.gov (United States)

    Wang, Rongyu; Ma, Hongmin; Zhang, Yong; Wang, Qi; Yang, Zhongping; Du, Bin; Wu, Dan; Wei, Qin

    2017-10-15

    An ultrasensitive photoelectrochemical sandwich immunosensor was designed for detection of insulin based on WO 3 /CdS/polydopamine (WO 3 /CdS/PDA) co-sensitized and PDA@carbon nanotubes (PDA@CNT) conjugates for signal amplification. The CdS nanoparticles were first deposited on the WO 3 nanorods via sequential chemical bath deposition to form the WO 3 /CdS structure to enhance photocurrent. Then equipped with PDA to form the WO 3 /CdS/PDA photosensitive structure. The PDA was used not only to reduce the toxicity of CdS but also adsorb insulin primary antibodies (Ab 1 ). Meanwhile, insulin secondary antibodies (Ab 2 ) were decorated by PDA@CNT conjugates for signal amplification and further enhance photocurrent. Different photocurrent intensities were obtained by the photoelectrochemical workstation at applied bias of 0V due to the different amount of the PDA@CNT conjugates introduced by the different concentrations of insulin. A good linear relationship was obtained between the increased photocurrent and insulin concentrations range from 0.01ngmL -1 to 50ngmL -1 . And a detection limit of 2.8pgmL -1 was obtained. The proposed sensor was applied to the determination of the insulin in human serum sample, and satisfactory results were obtained. The sensor presented good specificity, reproducibility and stability, thus it might find application in the clinical diagnosis of insulin or other biomarkers in the near future. Copyright © 2017 Elsevier B.V. All rights reserved.

  5. Visible-light photocatalytic activity of Ag2O coated Bi2WO6 hierarchical microspheres assembled by nanosheets

    International Nuclear Information System (INIS)

    Chen, Lin; Hua, Hao; Yang, Qi; Hu, Chenguo

    2015-01-01

    Graphical abstract: - Highlights: • Bi 2 WO 6 hierarchical microspheres assembled by nanosheets and dispersed nanosheets are synthesized. • Ag 2 O/Bi 2 WO 6 heterostuctures exhibites an enhanced photocatalytic activity compared with the Bi 2 WO 6 nanostructures. • Photocatalytic activity of the Ag 2 O/Bi 2 WO 6 microspheres is higher than that of the nanosheets. • Bi 2 WO 6 hierarchical structure is an excellent architecture for loading of Ag 2 O nanoparticles. - Abstract: Bi 2 WO 6 hierarchical microspheres assembled by nanosheets and dispersed nanosheets were synthesized by hydrothermal reaction in different conditions. Ag 2 O nanoparticles were deposited on the surface of Bi 2 WO 6 microspheres and nanosheets by the chemical precipitation method. The photocatalytic performance of pure Bi 2 WO 6 nanostructures and Ag 2 O/Bi 2 WO 6 heterostructures were evaluated by the photocatalytic decolorization of RhB solution under visible-light irradiation. Compared with the pure Bi 2 WO 6 nanostructures, the Ag 2 O/Bi 2 WO 6 heterostructures exhibited an obviously enhanced photocatalytic activity. And photocatalytic activity of the Ag 2 O/Bi 2 WO 6 microspheres is higher than that of the Ag 2 O/Bi 2 WO 6 nanosheets. This work demonstrates that the Bi 2 WO 6 hierarchical three-dimensional structure is an excellent architecture for the loading of Ag 2 O nanoparticles to build a highly efficient photocatalyst

  6. Morphologically different WO3 nanocrystals in photoelectrochemical water oxidation

    International Nuclear Information System (INIS)

    Biswas, Soumya Kanti; Baeg, Jin-Ook; Moon, Sang-Jin; Kong, Ki-jeong; So, Won-Wook

    2012-01-01

    Different morphologies of WO 3 nanocrystals such as nanorods and nanoplates have been obtained under hydrothermal conditions using ammonium metatungstate as the precursor in presence of different organic acids such as citric, oxalic, and tartaric acid in the reaction medium. Detailed characterization of the crystal structure, particle morphology, and optical band gap of the synthesized powders have been done by X-ray diffraction, transmission electron microscopy, scanning electron microscopy and solid-state UV–visible spectroscopy study. The as-synthesized materials are WO 3 hydrates with orthorhombic phase which transform to the hexagonal WO 3 through dehydration upon heating at 350 °C. The resultant products are crystalline with nanoscale dimensions. Finally, the photoactivity of the synthesized materials annealed at 500 °C has been compared employing in photoelectrochemical water oxidation under the illumination of AM 1.5G simulated solar light (100 mWcm −2 ). The photocurrent measurements upon irradiation of light exhibit obvious photocatalytic activity with a photocurrent of about 0.77, 0.61, and 0.65 mAcm −2 for the WO 3 film derived with the oxalic acid, tartaric, and citric acid assisting agents, respectively, at 1.8 V versus Ag/AgCl electrode.

  7. Monoclonal antibody-based broad-specificity immunoassay for monitoring organophosphorus pesticides in environmental water samples

    Science.gov (United States)

    The extensive use of organophosphorus pesticides (OPs) in agriculture and domestic settings can result in widespread water contamination. The development of easy-to-use and rapid-screening immunoassay methods in a class-selective manner is a topic of considerable environmental interest. In this wo...

  8. Biomimetic fabrication of WO{sub 3} for water splitting under visible light with high performance

    Energy Technology Data Exchange (ETDEWEB)

    Yin, Chao; Zhu, Shenmin, E-mail: smzhu@sjtu.edu.cn; Yao, Fan; Gu, Jiajun; Zhang, Wang [Shanghai Jiao Tong University, State Key Laboratory of Metal Matrix Composites (China); Chen, Zhixin [University of Wollongong, Faculty of Engineering (Australia); Zhang, Di, E-mail: zhangdi@sjtu.edu.cn [Shanghai Jiao Tong University, State Key Laboratory of Metal Matrix Composites (China)

    2013-08-15

    Inspired by the high light-harvesting properties of typical butterfly wings, ceramic WO{sub 3} butterfly wings with hierarchical structures of bio-butterfly wings was fabricated using a template of PapilioParis butterfly wings through a sol-gel method. The effect of calcination temperatures on the structures of the ceramic butterfly wings was investigated and the results showed that the WO{sub 3} butterfly wing replica calcined at 550 Degree-Sign C (WO{sub 3} replica-550) is a single phase and has a high crystallinity and relatively fine hierarchical structure. The average grain size of WO{sub 3} replica-550 and WO{sub 3} powder are around 32.6 and 42.2 nm, respectively. Compared with pure WO{sub 3} powder, WO{sub 3} replica-550 demonstrated a higher light-harvesting capability in the region from 460 to 700 nm and more importantly the higher charge separation rate, as evidenced by electron paramagnetic resonance measurements. Photocatalytic O{sub 2} evolutions from water were investigated on the ceramic butterfly wings and pure WO{sub 3} powder under visible light ({lambda} > 420 nm). The results showed that the amount of O{sub 2} produced from WO{sub 3} replica-550 is 50 % higher than that of the pure WO{sub 3} powder. The improved photocatalytic performance of WO{sub 3} replica-550 is attributed to the quasi-honeycomb structure inherited from the PapilioParis butterfly wings, providing both high light-harvesting efficiency and efficient charge transport through the WO{sub 3}.

  9. Red photoluminescent property and modification of WO3:Eu3+ inverse opal for blue light converted LEDs

    Science.gov (United States)

    Ruan, Jiufeng; Yang, Zhengwen; Huang, Anjun; Chai, Zhuangzhuang; Qiu, Jianbei; Song, Zhiguo

    2018-01-01

    Blue light converted light-emitting diodes is of great significance as a candidate for next generation lighting. In this work, the WO3:Eu3+ inverse opal photonic crystals were prepared and their luminescence properties were studied. The results demonstrated that the main excitation peak of WO3:Eu3+ inverse opals were located at 465 nm. The red luminescence peak at the 613 nm was observed in the WO3:Eu3+ inverse opal upon 465 nm excitation, exhibiting better red color purity. The influence of photonic band gap on the photoluminescence of WO3:Eu3+ inverse opal was obtained. When the red luminescence peak is in the regions of the photonic band gap and the edge of the band-gap, the red luminescence suppression and enhancement was observed respectively. The WO3:Eu3+ inverse opals may be a promising candidate for the blue light converted LEDs.

  10. Preparation and properties of bio-compatible magnetic Fe3O4 nanoparticles

    International Nuclear Information System (INIS)

    Chan, H.T.; Do, Y.Y.; Huang, P.L.; Chien, P.L.; Chan, T.S.; Liu, R.S.; Huang, C.Y.; Yang, S.Y.; Horng, H.E.

    2006-01-01

    In this work, we study the preparation and properties of bio-compatible magnetic nanoparticles for immunoassay and DNA detection. The magnetite (Fe 3 O 4 ) nanoparticles were prepared by a chemical co-precipitation method and dextran was selected as the surfactant to suspend the nanoparticles. Suspended particles associated with avidin followed by biotin were qualitatively analyzed by enzyme-linked immunosorbent assay (ELISA) method. We found further the ethylenediamine blocked activated residual groups efficiently, hence enhancing the attachment of biotin for probing the avidin

  11. Structure, electrochromic and optical properties of WO3 film prepared by dip coating-pyrolysis

    International Nuclear Information System (INIS)

    Yang Haitao; Shang Fuliang; Gao Ling; Han Haitao

    2007-01-01

    The tungsten oxide (WO 3 ) film was grown by dip coating-pyrolysis method with the PEG-400 as the structure-directing agent. Microstructure of the WO 3 film was characterized by TG-DSC, XRD and SEM techniques. It was found that the film annealed at 350 deg. C for 2 h comprised cubic WO 3 and orthorhombic WO 3 . The measurements of the cyclic voltammetry (CV) and UV-vis spectrum suggested that the WO 3 film had a good electrochromic reversibility performance. The film possessed excellent modulation to the visible light and the maximal average transmittance modulation reached 70.06%

  12. The Role of Nanoparticle Design in Determining Analytical Performance of Lateral Flow Immunoassays.

    Science.gov (United States)

    Zhan, Li; Guo, Shuang-Zhuang; Song, Fayi; Gong, Yan; Xu, Feng; Boulware, David R; McAlpine, Michael C; Chan, Warren C W; Bischof, John C

    2017-12-13

    Rapid, simple, and cost-effective diagnostics are needed to improve healthcare at the point of care (POC). However, the most widely used POC diagnostic, the lateral flow immunoassay (LFA), is ∼1000-times less sensitive and has a smaller analytical range than laboratory tests, requiring a confirmatory test to establish truly negative results. Here, a rational and systematic strategy is used to design the LFA contrast label (i.e., gold nanoparticles) to improve the analytical sensitivity, analytical detection range, and antigen quantification of LFAs. Specifically, we discovered that the size (30, 60, or 100 nm) of the gold nanoparticles is a main contributor to the LFA analytical performance through both the degree of receptor interaction and the ultimate visual or thermal contrast signals. Using the optimal LFA design, we demonstrated the ability to improve the analytical sensitivity by 256-fold and expand the analytical detection range from 3 log 10 to 6 log 10 for diagnosing patients with inflammatory conditions by measuring C-reactive protein. This work demonstrates that, with appropriate design of the contrast label, a simple and commonly used diagnostic technology can compete with more expensive state-of-the-art laboratory tests.

  13. Facile Hydrogen Evolution Reaction on WO3Nanorods

    Directory of Open Access Journals (Sweden)

    Rajeswari Janarthanan

    2007-01-01

    Full Text Available AbstractTungsten trioxide nanorods have been generated by the thermal decomposition (450 °C of tetrabutylammonium decatungstate. The synthesized tungsten trioxide (WO3 nanorods have been characterized by XRD, Raman, SEM, TEM, HRTEM and cyclic voltammetry. High resolution transmission electron microscopy and X-ray diffraction analysis showed that the synthesized WO3nanorods are crystalline in nature with monoclinic structure. The electrochemical experiments showed that they constitute a better electrocatalytic system for hydrogen evolution reaction in acid medium compared to their bulk counterpart.

  14. Investigation of the La2O3-Nb2O5-WO3 ternary phase diagram: Isolation and crystal structure determination of the original La3NbWO10 material

    KAUST Repository

    Vu, T.D.; Vu, T.D.; Barre, M.; Adil, Karim; Jouanneaux, A.; Suard, E.; Goutenoire, F.

    2015-01-01

    In the course of the exploration of the La2O3-WO3-Nb2O5 ternary phase diagram, a new compound with the formula La3NbWO10 was discovered. Its structure was determined from a combination of powder X-ray and neutron diffraction data. It crystallizes

  15. Chitosan Fibers Modified with HAp/β–TCP Nanoparticles

    Directory of Open Access Journals (Sweden)

    Dariusz Wawro

    2011-10-01

    Full Text Available This paper describes a method for preparing chitosan fibers modified with hydroxyapatite (HAp, tricalcium phosphate (β-TCP, and HAp/β-TCP nanoparticles. Fiber-grade chitosan derived from the northern shrimp (Pandalus borealis and nanoparticles of tricalcium phosphate (β-TCP and hydroxyapatite (HAp suspended in a diluted chitosan solution were used in the investigation. Diluted chitosan solution containing nanoparticles of Hap/β-TCP was introduced to a 5.16 wt% solution of chitosan in 3.0 wt% acetic acid. The properties of the spinning solutions were examined. Chitosan fibers modified with nanoparticles of HAp/β-TCP were characterized by a level of tenacity and calcium content one hundred times higher than that of regular chitosan fibers.

  16. Design of Cobalt Nanoparticles with Tailored Structural and Morphological Properties via O/W and W/O Microemulsions and Their Deposition onto Silica

    Directory of Open Access Journals (Sweden)

    Gabriella Di Carlo

    2015-03-01

    Full Text Available Cobalt nanostructures with different size and morphology, i.e., spherical nanoparticles, nanorods, and particles arranged into elongated structures, were prepared using micelles and microemulsions as confined reaction media. The syntheses were carried out using three types of systems: aqueous surfactant solutions, oil-in water (O/W, and water-in-oil (W/O microemulsions. The influence of the surfactant and the precipitating agent used for synthesis was also investigated. For this purpose, cobalt nanostructures were prepared using different non-ionic surfactants, namely Synperonic® 10/6, Pluronic® P123 and a mixture of SPAN 20–TWEEN 80. Three different precipitating agents were used: sodium borohydride, sodium hydroxide, and oxalic acid. Our findings revealed that by changing the type of reaction media as well as the precipitating agent it is possible to modify the shape and size of the cobalt nanostructures. Moreover, the use of O/W microemulsion generates better results in terms of colloidal stability and uniformity of particle size with respect to W/O microemulsion. The different cobalt nanostructures were supported on commercial and mesoporous silica; transmission electron microscopy (TEM images showed that after deposition the Co nanocrystals remain well dispersed on the silica supports. This behavior suggests their great potential in catalytic applications.

  17. Highly sensitive immunoassay of protein molecules based on single nanoparticle fluorescence detection in a nanowell

    Science.gov (United States)

    Han, Jin-Hee; Kim, Hee-Joo; Lakshmana, Sudheendra; Gee, Shirley J.; Hammock, Bruce D.; Kennedy, Ian M.

    2011-03-01

    A nanoarray based-single molecule detection system was developed for detecting proteins with extremely high sensitivity. The nanoarray was able to effectively trap nanoparticles conjugated with biological sample into nanowells by integrating with an electrophoretic particle entrapment system (EPES). The nanoarray/EPES is superior to other biosensor using immunoassays in terms of saving the amounts of biological solution and enhancing kinetics of antibody binding due to reduced steric hindrance from the neighboring biological molecules. The nanoarray patterned onto a layer of PMMA and LOL on conductive and transparent indium tin oxide (ITO)-glass slide by using e-beam lithography. The suspension of 500 nm-fluorescent (green emission)-carboxylated polystyrene (PS) particles coated with protein-A followed by BDE 47 polyclonal antibody was added to the chip that was connected to the positive voltage. The droplet was covered by another ITO-coated-glass slide and connected to a ground terminal. After trapping the particles into the nanowells, the solution of different concentrations of anti-rabbit- IgG labeled with Alexa 532 was added for an immunoassay. A single molecule detection system could quantify the anti-rabbit IgG down to atto-mole level by counting photons emitted from the fluorescent dye bound to a single nanoparticle in a nanowell.

  18. Fe3O4 nanoparticles modified by CD-containing star polymer for MRI and drug delivery.

    Science.gov (United States)

    Cha, Ruitao; Li, Juanjuan; Liu, Yang; Zhang, Yifan; Xie, Qian; Zhang, Mingming

    2017-10-01

    Fe 3 O 4 nanoparticles with ultrasmall sizes show good T 1 or T 1 +T 2 contrast abilities, and have attracted considerable interest in the field of magnetic resonance imaging (MRI) contrast agents. For effective biomedical applications, the colloidal stability and biocompatibility of the Fe 3 O 4 nanoparticles need to be improved without reducing MRI relaxivity. In this paper, star polymers were used as coating materials to modify Fe 3 O 4 nanoparticles in view of their dense molecular architecture with moderate flexibility. The star polymer was composed of a β-cyclodextrin (β-CD) core and poly(2-(dimethylamino) ethyl methacrylate) (PDMAEMA) arms. Meanwhile, reduced glutathione (GSH), as a model drug, was also associated with the star polymer. Thus, a new platform for simultaneous diagnosis and treatment was achieved. Compared to the Fe 3 O 4 nanoparticles coated with linear polymers, the Fe 3 O 4 nanoparticles coated with star polymers (Fe 3 O 4 @GCP) possessed higher GSH association capacity and better stability in serum-containing solution. GSH could be released from Fe 3 O 4 @GCP nanoparticles in response to pH value of the solution. Since the sulfhydryl group on GSH is able to combine free radicals, Fe 3 O 4 @GCP nanoparticles exhibited less cytotoxicity compared to the Fe 3 O 4 nanoparticles without including GSH. Furthermore, the nanoparticles could also serve as good T 1 MRI contrast agent, and the MRI relaxivity of Fe 3 O 4 @GCP nanoparticles did not decrease after coated with the star polymer. These results indicate that the precisely designed Fe 3 O 4 @GCP nanoparticles could be used as a versatile promising theranostic nano-platform. Copyright © 2017 Elsevier B.V. All rights reserved.

  19. Gas Sensing Properties of Pure and Cr Activated WO3 Thick Film Resistors

    Directory of Open Access Journals (Sweden)

    V. B. GAIKWAD

    2010-09-01

    Full Text Available Thick films of WO3 (Tungsten Oxide were prepared by screen-printing techniques. The surfaces of the films were modified by dipping them into an aqueous solution of Chromium Oxide (CrO3 for different intervals of time, followed by firing at 550 oC for 30 min. The gas sensing performance of the pure and Cr2O3-modified films was tested for various gases at different temperatures. The unmodified films showed response to H2S, ethanol and cigar smoke. However Cr2O3- modified films suppresses gas sensing response to all gases except H2S. The surface modification, using dipping process, altered the adsorbate-adsorbent interactions, which gave the specific selectivity and enhanced sensitivity to H2S gas. The gas response, selectivity, thermal stability and recovery time of the sensor were measured and presented. The role played by surface chromium species to improve gas sensing performance is discussed.

  20. Correlations among structure, composition and electrochemical performances of WO3 anode materials for lithium ion batteries

    International Nuclear Information System (INIS)

    Li, Pu; Li, Xing; Zhao, Ziyan; Wang, Mingshan; Fox, Thomas; Zhang, Qian; Zhou, Ying

    2016-01-01

    Highlights: • The residual precursor ions affect the charge/discharge performances of WO 3 . • Lithiated monoclinic WO 3 reveals the best discharge capacity. • Lithiation can enhance the conductivity of WO 3 . - Abstract: Suitable host structure for lithium insertion and extraction is crucial for lithium-ion batteries. Tungsten trioxides (WO 3 ) are particularly interesting materials for this purpose. In this work, the influences of structure and composition of WO 3 on the charge/discharge performances of Li-ion batteries are systematically investigated. Firstly, lithiated tungsten trioxides (Li-WO 3 ) are successfully synthesized by a hydrothermal method followed by annealing at different temperatures (200–600 °C). It is found that the hexagonal framework collapses and gradually transforms to the monoclinic phase due to the release of NH 4 + and NH 3 molecules. Unexpectedly, monoclinic WO 3 reveals better performances than that of hexagonal WO 3 . Among all the investigated samples, the lithiated WO 3 annealed at 500 °C exhibits the highest discharge capacity and cycle performance (703 mAh g −1 after 10 cycles). We believe that the Li + remained in the solid structure of WO 3 can lead to a more stable structure. In addition, Li + could inhibit the oxidation of W 5+ during the heat treatment process, which increases the electron conductivity of WO 3 . Our results indicate that the electrochemical properties of WO 3 are strongly related to the residual precursor and crystal structure.

  1. Fabrication of the heterostructured CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} hybrid photocatalyst with enhanced performance of photocatalytic hydrogen production from water

    Energy Technology Data Exchange (ETDEWEB)

    Lang, Junyu; Liu, Mengqing; Su, Yiguo; Yan, Lijuan; Wang, Xiaojing, E-mail: wang_xiao_jing@hotmail.com

    2015-12-15

    Graphical abstract: - Highlights: • A novel ternary CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} hybrid photocatalyst was successfully fabricated. • Au particles act as an electron-conduction bridge between the heterostructure. • The photoctalytic hydrogen generation was promoted by the SPR of the Au. • CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} shows significant photocatalytic activity in H{sub 2} generation. - Abstract: In this work, a novel CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} hybrid photocatalyst is successfully fabricated. The photocatalytic performance of the heterostructured CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} composite was investigated. Au nanoparticles were photo-deposited as the interlayer between g-C{sub 3}N{sub 4} and the surface of CsTaWO{sub 6}, which can facilitate the photoinduced electrons migration as an electron-conduction bridge as well as increase visible-light absorption via the surface plasmon resonance. This heterostructured interface bridging by Au particles may significantly retard the recombination of electron–holes, which is beneficial to promote the photocatalytic activity under visible-light irradiation. It is found the CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} sample showed excellent photocatalytic activity of water splitting, even higher than the sum of g-C{sub 3}N{sub 4} and Au/CsTaWO{sub 6} samples, or the sum of CsTaWO{sub 6} and Au/g-C{sub 3}N{sub 4} samples. It indicates that the heterostructured combination of g-C{sub 3}N{sub 4} and CsTaWO{sub 6} bridging by Au particles provided the synergistic photocatalytic activity driving by solar light through an efficient electron transfer process.

  2. Constructing 2D layered MoS2 nanosheets-modified Z-scheme TiO2/WO3 nanofibers ternary nanojunction with enhanced photocatalytic activity

    Science.gov (United States)

    Zhao, Jiangtao; Zhang, Peng; Fan, Jiajie; Hu, Junhua; Shao, Guosheng

    2018-02-01

    Advanced materials for photoelectrochemical H2 production are important to the field of renewable energy. Despite great efforts have been made, the present challenge in materials science is to explore highly active photocatalysts for splitting of water at low cost. In this work, we report a new composite material consisting of 2D layered MoS2 nanosheets grown on the presence of TiO2/WO3 nanofibers (TW) as a high-performance photocatalyst for H2 evolution. This composite material was prepared by a two-step simple process of electrospinning and hydrothermal. We found that the as-prepared TiO2/WO3@MoS2 (TWM) hybrid exhibited superior photocatalytic activity in the hydrogen evolution reaction (HER) even without the noble metal-cocatalyst. Importantly, the TiO2/WO3@MoS2 heterostructure with 60 wt% of MoS2 exhibits the highest hydrogen production rate. This great improvement is attributed to the positive synergetic effect between the WO3 and MoS2 components in this hybrid cocatalyst, which serve as hole collector and electron collector, respectively. Moreover, the effective charge separation was directly proved by ultraviolet photoelectron spectroscopy, electrochemical impedance spectroscopy, and photocurrent analysis.

  3. Visible-light active thin-film WO3 photocatalyst with controlled high-rate deposition by low-damage reactive-gas-flow sputtering

    Directory of Open Access Journals (Sweden)

    Nobuto Oka

    2015-10-01

    Full Text Available A process based on reactive gas flow sputtering (GFS for depositing visible-light active photocatalytic WO3 films at high deposition rates and with high film quality was successfully demonstrated. The deposition rate for this process was over 10 times higher than that achieved by the conventional sputtering process and the process was highly stable. Furthermore, Pt nanoparticle-loaded WO3 films deposited by the GFS process exhibited much higher photocatalytic activity than those deposited by conventional sputtering, where the photocatalytic activity was evaluated by the extent of decomposition of CH3CHO under visible light irradiation. The decomposition time for 60 ppm of CH3CHO was 7.5 times more rapid on the films deposited by the GFS process than on the films deposited by the conventional process. During GFS deposition, there are no high-energy particles bombarding the growing film surface, whereas the bombardment of the surface with high-energy particles is a key feature of conventional sputtering. Hence, the WO3 films deposited by GFS should be of higher quality, with fewer structural defects, which would lead to a decrease in the number of centers for electron-hole recombination and to the efficient use of photogenerated holes for the decomposition of CH3CHO.

  4. Sensitive electrochemical determination of α-fetoprotein using a glassy carbon electrode modified with in-situ grown gold nanoparticles, graphene oxide and MWCNTs acting as signal amplifiers

    International Nuclear Information System (INIS)

    Gao, Yan-Sha; Zhu, Xiao-Fei; Yang, Tao-Tao; Xu, Jing-Kun; Zhang, Kai-Xin; Lu, Li-Min

    2015-01-01

    The authors describe an electrochemical immunoassay for α-fetoprotein (α-FP) using a glassy carbon electrode (GCE) modified with a nanocomposite made from gold nanoparticles, graphene oxide and multi-walled carbon nanotubes (AuNPs/GO-MWCNTs) and acting as a signal amplification matrix. The nanocomposite was synthesized in a one-pot redox reaction between GO and HAuCl 4 without using an additional reductant. The stepwise assembly of the immunoelectrode was characterized by means of cyclic voltammetry and electrochemical impedance spectroscopy. The interaction of antigen and antibody on the surface of the electrode creates a barrier for electrons and causes retarded electron transfer, this resulting in decreased signals in differential pulse voltammetry of hexacyanoferrate which is added as an electrochemical probe. Using this strategy and by working at a potential of 0.2 V (vs. SCE), a wide analytical range (0.01 - 100 ng∙mL -1 ) is covered. The correlation coefficient is 0.9929, and the limit of detection is as low as 3 pg∙mL -1 at a signal-to-noise ratio of 3. This electrochemical immunoassay combines the specificity of an immunological detection scheme with the sensitivity of an electrode modified with AuNPs and GO-MWCNTs. (author)

  5. Luminescence and thermoluminescence properties of Sr{sub 3}WO{sub 6}:Eu{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Emen, F.M., E-mail: femen106@gmail.com [Department of Chemistry, Faculty of Arts and Science, Mehmet Akif Ersoy University, TR 15030, Burdur (Turkey); Altinkaya, R. [Department of Chemistry, Faculty of Arts and Science, Mersin University, TR 33343, Mersin (Turkey)

    2013-02-15

    Sr{sub 3-x}WO{sub 6}:xEu{sup 3+} (x varies from 0.01 to 0.06) phosphors have been prepared at high temperature by the solid-state method. The crystal structure of Sr{sub 2.95}WO{sub 6}:0.05Eu{sup 3+} phosphor has been determined as a triclinic P-1 space group with a=8.3608 (19) A, b=8.2903 (24) A, c=8.2145 (23) A, {alpha}=89.79 (3){sup Degree-Sign }, {beta}=89.82 (3){sup Degree-Sign }, and {gamma}=89.753 (22){sup Degree-Sign }. The excitation spectrum of Sr{sub 2.95}WO{sub 6}:0.05Eu{sup 3+} phosphor reveals five excitation bands: one is assigned to the charge-transfer (CTLM) band of Sr{sub 3}WO{sub 6} host at 307 nm, and another is assigned to intra-4f transitions between 393 nm and 600 nm. The emission spectrum of Sr{sub 2.95}WO{sub 6}:0.05Eu{sup 3+} phosphor exhibits a series of emission bands, which are attributed to the {sup 5}D{sub 0}{yields}{sup 7}F{sub j} (j=0-4) transitions of Eu{sup 3+} ions. The luminescence studies revealed that the Eu{sup 3+} ions show high luminescent efficiency in emitting red light at 616 nm. The thermoluminescence glow curve shows one dominant glow peak observed at 56 Degree-Sign C which is related to the defects at shallow trap depth. The trap parameters mainly activation energy (E{sub a}) and the order of the kinetics (b) were evaluated by using Rasheedy's three points method (TPM). - Highlights: Black-Right-Pointing-Pointer The Sr{sub 3}WO{sub 6}:Eu{sup 3+} phosphor was prepared by using conventional ceramic method. Black-Right-Pointing-Pointer The diffraction peaks of phosphor have been indexed to triclinic system. Black-Right-Pointing-Pointer The emission peak at 616 nm belongs to {sup 5}D{sub 0}{yields}{sup 7}F{sub 2} electric dipole transitions of Eu{sup 3+}. Black-Right-Pointing-Pointer The emission band of WO{sub 6} and excitation bands of Eu{sup 3+} are overlapping each other. Black-Right-Pointing-Pointer The energy transfer from WO{sub 6} groups to the Eu{sup 3+} ions occurs under the UV excitation.

  6. Physical properties characterization of WO3 films grown by hot-filament metal oxide deposition

    International Nuclear Information System (INIS)

    Diaz-Reyes, J.; Delgado-Macuil, R.J.; Dorantes-Garcia, V.; Perez-Benitez, A.; Balderas-Lopez, J.A.; Ariza-Ortega, J.A.

    2010-01-01

    WO 3 is grown by hot-filament metal oxide deposition (HFMOD) technique under atmospheric pressure and an oxygen atmosphere. By X-ray diffraction obtains that WO 3 presents mainly monoclinic crystalline phase. The chemical stoichiometry is obtained by X-ray Photoelectron Spectroscopy (XPS). The IR spectrum of the as-grown WO 3 presents broad peaks in the range of 1100 to 3600 cm -1 . A broad band in the 2200 to 3600 cm -1 region and the peaks sited at 1645 and 1432 cm -1 are well resolved, which are originated from moisture and are assigned to ν(OH) and δ(OH) modes of adsorbed water and the corresponding tungsten oxide vibrations are in infrared region from 400 to 1453 cm -1 and around 3492 cm -1 , which correspond to tungsten-oxygen (W-O) stretching, bending and lattice modes. The Raman spectrum shows intense peaks at 801, 710, 262 and 61 cm -1 that are typical Raman peaks of crystalline WO 3 (m-phase) that correspond to stretching vibrations of the bridging oxygen, which are assigned to W-O stretching (ν) and W-O bending (δ) modes, respectively. By transmittance measurements obtains that the WO 3 band gap can be varied from 2.92 to 3.13 eV in the investigated annealing temperature range.

  7. Characterisation and application of WO3 films for electrochromic devices

    Science.gov (United States)

    Stapinski, Thomas; Marszalek, Konstanty; Swatowska, Barbara; Stanco, Agnieszka

    2013-07-01

    Electrochromic system is the one of the most popular devices using color memory effect under the influence of an applied voltage. The electrochromic system was produced based on the thin WO3 electrochromic films. Films were prepared by RF magnetron sputtering from tungsten targets in a reactive Ar+O2 gas atmosphere of various Ar/O2 ratios. The technological gas mixture pressure was 3 Pa and process temperature 30°C. Structural and optical properties of WO3 films were investigated for as-deposited and heat treated samples at temperature range from 350°C to 450°C in air. The material revealed the dependence of properties on preparation conditions and on post-deposition heat treatment. Main parameters of thin WO3 films: thickness d, refractive index n, extinction coefficient k and energy gap Eg were determined and optimized for application in electrochromic system. The main components of the system were glass plate with transparent conducting oxides, electrolyte, and glass plate with transparent conducting oxides and WO3 layer. The optical properties of the system were investigated when a voltage was applied across it. The electrochromic cell revealed the controllable transmittance depended on the operation voltage.

  8. Constructing superhydrophobic WO3@TiO2 nanoflake surface beyond amorphous alloy against electrochemical corrosion on iron steel

    Science.gov (United States)

    Yu, S. Q.; Ling, Y. H.; Wang, R. G.; Zhang, J.; Qin, F.; Zhang, Z. J.

    2018-04-01

    To eliminate harmful localized corrosion, a new approach by constructing superhydrophobic WO3@TiO2 hierarchical nanoflake surface beyond FeW amorphous alloy formed on stainless steel was proposed. Facile dealloying and liquid deposition was employed at low temperature to form a nanostructured layer composing inner WO3 nanoflakes coated with TiO2 nanoparticles (NPs) layer. After further deposition of PFDS on nanoflakes, the contact angle reached 162° while the corrosion potential showed a negative shift of 230 mV under illumination, resulting in high corrosion resistance in 3.5 wt% NaCl solution. The tradeoff between superhydrophobic surface and photo-electro response was investigated. It was found that this surface feature makes 316 SS be immune to localized corrosion and a pronounced photo-induced process of electron storage/release as well as the stability of the functional layer were detected with or without illumination, and the mechanism behind this may be related to the increase of surface potential due to water repellence and the delayed cathodic protection of semiconducting coating derived mainly from the valence state changes of WO3. This study demonstrates a simple and low-cost electrochemical approach for protection of steel and novel means to produce superhydrophobic surface and cathodic protection with controllable electron storage/release on engineering scale.

  9. Increasing of sensitivity of fluorescent immunoassay analysis of alpha-fetoprotein by means of plasmonical silver nanoparticles

    International Nuclear Information System (INIS)

    Vashchenko, S.V.; Min'ko, A.A.; Romanenko, A.A.; Gaponenko, S.V.; Kulakovich, O.S.

    2014-01-01

    A test system is proposed based on metal enhanced fluorescence to analyze low concentrations of alpha-fetoprotein (AFP), a tumor marker. Antigen-antibody reaction was performed on polystyrene plates coated with silver nanoparticles to increase sensitivity of fluorescent immunoassay and signal-to-noise ratio as compared to silver-free system. As compared to widely used ELISA technique and other immunoassay techniques the proposed approach is characterized by smaller probe volume, fast analysis and simplicity. The proposed test system uses layer-by-layer assembly approach, LED excitation and nanowatt photodetection set-up. The proposed test system offers AFP detection at concentrations used in clinical practice. Fluorescence enhancement for labeled AFP antibodies on a silver substrate was found to depend on antibodies concentration and was up to 6 times. (authors)

  10. Facile synthesis of NiWO4/reduced graphene oxide nanocomposite with excellent capacitive performance for supercapacitors

    International Nuclear Information System (INIS)

    Xu, Xiaowei; Pei, Liyuan; Yang, Yang; Shen, Jianfeng; Ye, Mingxin

    2016-01-01

    NiWO 4 /reduced graphene oxide (NWG) nanocomposite was successfully synthesized through a facile one-pot solvothermal method for the first time. The resulting nanocomposite is composed of NiWO 4 nanoparticles that are uniformly attached on graphene sheets by in situ reducing. The as-prepared NWG composite has been systematically characterized by Powder X-ray diffraction, Fourier transform infrared spectra, Raman spectroscopy, Thermogravimetric analysis, Scanning electron microscopy, Transmission electron microscopy, X-ray photoelectron spectra, and Brunauer–Emmett–Teller analysis. The capacitive performances of the as-prepared NWG composite as electrode material are investigated. It is found that the NWG composite exhibits a high specific capacitance up to 1031.3 F g −1 at a current density of 0.5 A g −1 . The greatly enhanced capacitive performance of the NWG electrode can be attributed to the synergetic effect of NiWO 4 nanoparticles and RGO, which provides conducting channels and active sites. The cyclic stability tests demonstrated no decreases of its initial values after 5000 cycles, suggesting that such hybrid electrode possesses a great potential application in energy-storage devices. - Highlights: • NiWO 4 /RGO composite was successfully prepared through a facile solvothermal method. • The NiWO 4 /RGO composite shows a high specific capacitance of 1031.3 F g −1 . • Enhanced electrical conductivity leads to superior electrochemical performance.

  11. Ag2WO4 nanorods decorated with AgI nanoparticles: Novel and efficient visible-light-driven photocatalysts for the degradation of water pollutants

    Directory of Open Access Journals (Sweden)

    Shijie Li

    2018-04-01

    Full Text Available To develop efficient and stable visible-light-driven (VLD photocatalysts for pollutant degradation, we synthesized novel heterojunction photocatalysts comprised of AgI nanoparticle-decorated Ag2WO4 nanorods via a facile method. Various characterization techniques, including XRD, SEM, TEM, EDX, and UV–vis DRS were used to investigate the morphology and optical properties of the as-prepared AgI/Ag2WO4 catalyst. With AgI acting as the cocatalyst, the resulting AgI/Ag2WO4 heterostructure shows excellent performance in degrading toxic, stable pollutants such as rhodamine B (RhB, methyl orange (MO and para-chlorophenol (4-CP. The high performance is attributed to the enhanced visible-light absorption properties and the promoted separation efficiency of charge carriers through the formation of the heterojunction between AgI and Ag2WO4. Additionally, AgI/Ag2WO4 exhibits durable stability. The active species trapping experiment reveals that active species (O2•− and h+ dominantly contribute to RhB degradation. The AgI/Ag2WO4 heterojunction photocatalyst characterized in this work holds great potential for remedying environmental issues due to its simple preparation method and excellent photocatalytic performance.

  12. Surface Functionalization of WO3 Thin Films with (3-Aminopropyl)triethoxysilane and Succinic Anhydride

    Science.gov (United States)

    Ta, Thi Kieu Hanh; Tran, Thi Nhu Hoa; Tran, Quang Minh Nhat; Pham, Duy Phong; Pham, Kim Ngoc; Cao, Thi Thanh; Kim, Yong Soo; Tran, Dai Lam; Ju, Heongkyu; Phan, Bach Thang

    2017-06-01

    We report effects of oxygen plasma treatment on the surface functionalization of WO3 thin films with (3-aminopropyl)triethoxysilane (APTES) and succinic anhydride (SA). X-ray diffraction and x-ray photoelectron spectroscopy results indicate the existence of the WO3 phase. Fourier transform infrared spectroscopy measurement shows clear bands at 1040 cm-1 (Si-O-Si), 1556 cm-1 (N-H), 1655 cm-1 (C=O), 2937 cm-1 (C-H) and 3298 cm-1 (N-H), confirming the surface functionalization efficiency enhanced by prior treatment of oxygen plasma. It thus follows that the prior oxygen plasma treatment activates hydroxylation with more -OH groups on the WO3 surface, which can pave a highly efficient way to the surface functionalization by APTES and SA.

  13. Synthesis, characterization and photocatalytic activity of porous WO3/TiO2 hollow microspheres

    International Nuclear Information System (INIS)

    Yang, Liuyang; Si, Zhichun; Weng, Duan; Yao, Youwei

    2014-01-01

    Porous WO 3 /TiO 2 hollow microspheres were prepared by a spray drying method for photodegradation of methylene blue and phenol. The catalysts were characterized by X-ray diffraction, Field Emission Scanning Electron Microscope, High Resolution Transmission Electron Microscope, N 2 adsorption–desorption measurements, Raman spectrometer, UV–Vis Diffuse Reflectance Spectroscopy and Zeta-Meter measurements. The results showed that the tungsten oxides mainly existed in highly dispersed amorphous form on anatase when the loading amount of tungsten oxide was below 3 mol%. The improved photocatalytic activity under UV light irradiation of the WO 3 /TiO 2 catalyst mainly arises from the enhanced charge separation efficiency rather than the improved light absorbance by highly dispersed amorphous tungsten oxides. Highly dispersed amorphous WO x can form a shallowly trapped site due to its similar band structure with TiO 2 . The strongly electron-withdrawing of tungsten oxide in highly dispersed state facilitates the electron transition between titanium and WO x , and consequently improves the charge separation. The enhanced acidity of catalyst by WO x in reactant environment also improved the charge separation efficiency due to the timely transition of holes and electrons accumulated on TiO 2 and WO x , respectively. However, the improved photocatalytic activity under visible light irradiation of the WO 3 /TiO 2 catalyst mainly arises from light harvest. TiO 2 containing 3 mol% WO 3 displayed the highest photocatalytic activity under UV light irradiation while that containing 4 mol% WO 3 present highest activity under visible light irradiation

  14. Oxygen partial pressure effects on the magnetron sputtered WO3 films

    International Nuclear Information System (INIS)

    Muğlu, G Merhan; Gür, E

    2016-01-01

    Electrochromism is changing color of a substance in response to the applied an external electric field and the phenomenon is reversible. WO 3 is very attractive material due to its electrochromic properties as well as it is also attractive for many different applications such as gas sensors, phosphorous screen, textile, glass industry. In this study, it is aimed to provide optimization of the optical and structural characteristics of WO 3 by changing the growth parameters mainly the oxygen partial pressure. The partial pressure of oxygen was changed with increments of 0.7 mTorr. For the analysis, X-ray Diffraction (XRD), absorption, Raman spectroscopy measurements were used. When O 2 gas increased, peaks belong to the WO 3 was observed in XRD patterns at the 2 theta angles of 23.0, 11.0, 23.5 and 28.5 angles corresponding to the (002), (020) and (220) planes, respectively. This shows that there is a significant effect of increasing O 2 partial pressure in the formation of WO 3 films. The bandgap energy of the WO 3 thin films are found to be around 3.0 eV. Raman measurements showed vibrational modes of W-O-W stretching and bending modes which shows small shifts depending on the partial pressures of the O 2 . Obtained results indicated that better crystal structure is obtained with higher O 2 gas partial pressure. (paper)

  15. Hydrophobically modified chitosan/gold nanoparticles for DNA delivery

    International Nuclear Information System (INIS)

    Bhattarai, Shanta Raj; Remant Bahadur, K.C.; Aryal, Santosh; Bhattarai, Narayan; Kim, Sun Young; Yi, Ho Keun; Hwang, Pyoung Han; Kim, Hak Yong

    2008-01-01

    Present study dealt an application of modified chitosan gold nanoparticles (Nac-6-Au) for the immobilization of necked plasmid DNA. Gold nanoparticles stabilized with N-acylated chitosan were prepared by graft-onto approach. The stabilized gold nanoparticles were characterized by different physico-chemical techniques such as UV-vis, TEM, ELS and DLS. MTT assay was used for in vitro cytotoxicity of the nanoparticles into three different cell lines (NIH 3T3, CT-26 and MCF-7). The formulation of plasmid DNA with the nanoparticles corresponds to the complex forming capacity and in-vitro/in-vivo transfection efficiency was studied via gel electrophoresis and transfection methods, respectively. Results showed the modified chitosan gold nanoparticles were well-dispersed and spherical in shape with average size around 10∼12 nm in triple distilled water at pH 7.4, and showed relatively no cytotoxicity at low concentration. Addition of plasmid DNA on the aqueous solution of the nanoparticles markedly reduced surface potential (50.0∼66.6%) as well as resulted in a 13.33% increase in hydrodynamic diameters of the formulated nanoparticles. Transfection efficiency of Nac-6-Au/DNA was dependent on cell type, and higher β-galactosidase activity was observed on MCF-7 breast cancer cell. Typically, this activity was 5 times higher in 4.5 mg/ml nanoparticles concentration than that achieved by the nanoparticles of other concentrations (and/or control). However, this activity was lower in in-vitro and dramatically higher in in-vivo than that of commercially available transfection kit (Lipofectin (registered) ) and DNA. From these results, it can be expected to develop alternative new vectors for gene delivery

  16. Conductive surface modification of cauliflower-like WO3 and its electrochemical properties for lithium-ion batteries

    International Nuclear Information System (INIS)

    Yoon, Sukeun; Woo, Sang-Gil; Jung, Kyu-Nam; Song, Huesup

    2014-01-01

    Highlights: • Synthesis of cauliflower-like carbon-decorated WO 3 . • Superior cyclability and rate capability for cauliflower-like carbon-decorated WO 3 . • Electrochemical reaction behavior of cauliflower-like carbon-decorated WO 3 with lithium. • In-situ XRD analysis during the first discharge–charge shows a complex reaction of intercalation and conversion of WO 3 . - Abstract: Cauliflower-like WO 3 was synthesized by a hydrothermal reaction without a surfactant, followed by firing, and was investigated as an anode material for lithium-ion battery applications. The scanning electron microscope (SEM) and transmission electron microscope (TEM) characterization indicated that WO 3 nanorods had an aggregation framework and built a cauliflower morphology. With the objective of understanding the charge–discharge process within a voltage range of 0–3 V vs. Li + /Li, in situ X-ray diffraction was used and a complex reaction of intercalation and conversion of WO 3 was revealed for the first time. The cauliflower-like WO 3 after being decorated with carbon provides a high gravimetric capacity of >635 mA h/g (Li 5.5 WO 3 ) with good cycling and a high rate capability when used as an anode in lithium-ion batteries. Based on our studies, we attribute the high electrochemical performance to the nanoscopic WO 3 particles and a conductive carbon layer, which makes them a potential candidate for lithium-ion batteries

  17. WO3 nanoflakes decorated with CuO clusters for enhanced photoelectrochemical water splitting

    Directory of Open Access Journals (Sweden)

    Chongwu Wang

    2018-04-01

    Full Text Available The low quantum efficiency arising from poor charges transfer and insufficient light absorption is one of the critical challenges toward achieving highly efficient water splitting in photoelectrochemical cells. Three dimensions (3D structures and heterojunctions have received intensive research interests recent years due to their excellent ability to separate photo-generated charges as well as the enhanced light harvesting property. Herein, 3D CuO/WO3 structure was fabricated through a facile solvothermal method followed by chemical bath deposition. The loading of CuO clusters on WO3 nanoflake arrays results in a much improved photocurrent density compared with that of pristine WO3 nanoflake arrays, which reaches 1.8 mA/cm2 at 1.23 V vs. the reversible hydrogen electrode. The electrochemical impedance spectroscopy measurement demonstrates that the improved performance of CuO/WO3 electrode is attributed to the accelerated charge transfer kinetics as a result of the desirable band alignment in CuO/WO3 heterojunction. This work demonstrates a facile strategy to construct superior WO3 electrode, which will ultimately allow for efficient storage of solar energy into hydrogen. Keywords: Photoelectrochemistry, Water splitting, Tungsten trioxide photoanode, CuO clusters, Heterojunction

  18. Neuromorphic transistor achieved by redox reaction of WO3 thin film

    Science.gov (United States)

    Tsuchiya, Takashi; Jayabalan, Manikandan; Kawamura, Kinya; Takayanagi, Makoto; Higuchi, Tohru; Jayavel, Ramasamy; Terabe, Kazuya

    2018-04-01

    An all-solid-state neuromorphic transistor composed of a WO3 thin film and a proton-conducting electrolyte was fabricated for application to next-generation information and communication technology including artificial neural networks. The drain current exhibited a 4-order-of-magnitude increment by redox reaction of the WO3 thin film owing to proton migration. Learning and forgetting characteristics were well tuned by the gate control of WO3 redox reactions owing to the separation of the current reading path and pulse application path in the transistor structure. This technique should lead to the development of versatile and low-power-consumption neuromorphic devices.

  19. Towards TiO2 nanotubes modified by WO3 species: influence of ex situ crystallization of precursor on the photocatalytic activities of WO3/TiO2 composites

    Science.gov (United States)

    Sun, Hui; Dong, Bohua; Su, Ge; Gao, Rongjie; Liu, Wei; Song, Liang; Cao, Lixin

    2015-09-01

    TiO2 nanotubes (TNT) crystallized at different temperatures were loaded with WO3 hydrate through the reaction between (NH4)6W7O24·6H2O and an aqueous solution of HCl. The photocatalytic activities of nanocomposites firstly increase and then decrease as a function of the crystallized temperature of the TNT precursor. The structural, morphologic and optical properties of WO3/TiO2 nanocomposites were also investigated in this study. The samples, initially anatase titania (573 K-773 K), presented phase transition to rutile titania at 873 K. With the crystallized temperature increasing, an evolution of samples morphology changing from nanotube-like structure to nanorod-like structure was observed. Meanwhile, the absorption edge of samples exhibited a red shift, and correspondingly their band gap decreased. Consistent with x-ray diffraction diffractograms, the existence of rutile titania as an impurity in the precursor TNT, crystallized at higher than 873 K, depressed photocatalytic activity evidently. As a result, the degradation rate of methyl orange (MO) increased with the samples crystallinity firstly, and then reduced due to the appearance of rutile titania. In our experimental conditions, the optimal photocatalytic activity was achieved for the sample crystalized at 773 K. Its degradation rate could reach 98.76% after 90 min UV light irradiation.

  20. Towards TiO2 nanotubes modified by WO3 species: influence of ex situ crystallization of precursor on the photocatalytic activities of WO3/TiO2 composites

    International Nuclear Information System (INIS)

    Sun, Hui; Dong, Bohua; Su, Ge; Gao, Rongjie; Liu, Wei; Cao, Lixin; Song, Liang

    2015-01-01

    TiO 2 nanotubes (TNT) crystallized at different temperatures were loaded with WO 3 hydrate through the reaction between (NH 4 ) 6 W 7 O 24 ·6H 2 O and an aqueous solution of HCl. The photocatalytic activities of nanocomposites firstly increase and then decrease as a function of the crystallized temperature of the TNT precursor. The structural, morphologic and optical properties of WO 3 /TiO 2 nanocomposites were also investigated in this study. The samples, initially anatase titania (573 K–773 K), presented phase transition to rutile titania at 873 K. With the crystallized temperature increasing, an evolution of samples morphology changing from nanotube-like structure to nanorod-like structure was observed. Meanwhile, the absorption edge of samples exhibited a red shift, and correspondingly their band gap decreased. Consistent with x-ray diffraction diffractograms, the existence of rutile titania as an impurity in the precursor TNT, crystallized at higher than 873 K, depressed photocatalytic activity evidently. As a result, the degradation rate of methyl orange (MO) increased with the samples crystallinity firstly, and then reduced due to the appearance of rutile titania. In our experimental conditions, the optimal photocatalytic activity was achieved for the sample crystalized at 773 K. Its degradation rate could reach 98.76% after 90 min UV light irradiation. (paper)

  1. MIS gas sensors based on porous silicon with Pd and WO{sub 3}/Pd electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Solntsev, V.S. [Institute of Semiconductor Physics, National Academy of Science of Ukraine, 03028, Kiev (Ukraine); Gorbanyuk, T.I., E-mail: tatyanagor@mail.r [Institute of Semiconductor Physics, National Academy of Science of Ukraine, 03028, Kiev (Ukraine); Litovchenko, V.G.; Evtukh, A.A. [Institute of Semiconductor Physics, National Academy of Science of Ukraine, 03028, Kiev (Ukraine)

    2009-09-30

    Pd and WO{sub 3}/Pd gate metal-oxide-semiconductor (MIS) gas sensitive structures based on porous silicon layers are studied by the high frequency C(V) method. The chemical compositions of composite WO{sub 3}/Pd electrodes are characterized by secondary-ion mass spectrometry (SIMS). The atomic force microscopy (AFM) was used for morphologic studies of WO{sub 3}/Pd films. As shown in the experiments, WO{sub 3}/Pd structures are more sensitive and selective to the adsorption of hydrogen sulphide compared to Pd gate. The analyses of kinetic characteristics allow us to determine the response and characteristic times for these structures. The response time of MIS-structures with thin composite WO{sub 3}/Pd electrodes (the thickness of Pd is about 50 nm with WO{sub 3} clusters on its surface) is slower compared to the structures with Pd electrodes. Slower sensor responses of WO{sub 3}-based gas sensors may be associated with different mechanism of gas sensitivity of given structures. The enhanced sensitivity and selectivity to H{sub 2}S action of WO{sub 3}/Pd MIS-structures can also be explained by the chemical reaction that occurs at the catalytic active surface of gate electrodes. The possible mechanisms of enhanced sensitivity and selectivity to H{sub 2}S adsorption of MIS gas sensors with WO{sub 3}/Pd composite gate electrodes compared to pure Pd have been analyzed.

  2. Determination of avian influenza A (H9N2) virions by inductively coupled plasma mass spectrometry based magnetic immunoassay with gold nanoparticles labeling

    Science.gov (United States)

    Xiao, Guangyang; Chen, Beibei; He, Man; Shi, Kaiwen; Zhang, Xing; Li, Xiaoting; Wu, Qiumei; Pang, Daiwen; Hu, Bin

    2017-12-01

    Avian influenza viruses are the pathogens of global poultry epidemics, and may even cause the human infections. Here, we proposed a novel inductively coupled plasma mass spectrometry (ICP-MS) based immunoassay with gold nanoparticles (Au NPs) labeling for the determination of H9N2 virions. Magnetic-beads modified with anti-influenza A H9N2 hemagglutinin mono-antibody (mAb-HA) were utilized for the capture of H9N2 virions in complex matrix; and Au NPs conjugated with mAb-HA were employed for the specific labeling of H9N2 virions for subsequent ICP-MS detection. With a sandwich immunoassay strategy, this method exhibited a high specificity for H9N2 among other influenza A virions such as H1N1 and H3N2. Under the optimized conditions, this method could detect as low as 0.63 ng mL- 1 H9N2 virions with the linear range of 2-400 ng mL- 1, the relative standard deviation for seven replicate detections of H9N2 virions was 7.2% (c = 10 ng mL- 1). The developed method was applied for the detection of H9N2 virions in real-world chicken dung samples, and the recovery for the spiking samples was 91.4-116.9%. This method is simple, rapid, sensitive, selective, reliable and has a good application potential for virions detection in real-world samples.

  3. Chemical purification of CaCO{sub 3} and CaWO{sub 4} powders used for CaWO{sub 4} crystal production for the CRESST experiment

    Energy Technology Data Exchange (ETDEWEB)

    Trinh Thi, H.H.; Defay, X.; Erb, A.; Hampf, R.; Lanfranchi, J.C.; Langenkaemper, A.; Morgalyuk, V.; Muenster, A.; Mondragon, E.; Oppenheimer, C.; Potzel, W.; Schoenert, S.; Steiger, H.; Ulrich, A.; Wawoczny, S.; Willers, M.; Zoeller, A. [Physik-Department and Excellence Cluster Universe, Technische Universitaet Muenchen, Garching (Germany)

    2016-07-01

    CRESST (Cryogenic Rare Event Search with Superconducting Thermometers) uses CaWO{sub 4} single crystals as targets for the direct search for dark matter particles. Since several years these CaWO{sub 4} crystals are grown at the Technische Universitaet Muenchen. Thereby, commercially available CaCO{sub 3} and WO{sub 3} powders are used for the synthesis of CaWO{sub 4} powder. For the experiment low intrinsic contaminations of the crystals play a crucial role. In order to improve the radiopurity of the crystals it is necessary to reduce potential sources for radioactive backgrounds such as U and Th. In this poster we will present our studies of the chemical purification of the CaCO{sub 3} and CaWO{sub 4} powders.

  4. Solid-State Electrochromic Device Consisting of Amorphous WO3 and Various Thin Oxide Layers

    Science.gov (United States)

    Shizukuishi, Makoto; Shimizu, Isamu; Inoue, Eiichi

    1980-11-01

    A mixed oxide containing Cr2O3 was introduced into an amorphous WO3 solid-state electrochromic device (ECD) in order to improve its colour memory effect. The electrochromic characteristics were greatly affected by the chemical constituents of a dielectric layer on the a-WO3 layer. Particularly, long memory effect and low power dissipation were attained in a solid-state ECD consisting of a-WO3 and Cr2O3\\cdotV2O5(50 wt.%). Some electrochromic characteristics of the a-WO3/Cr2O3\\cdotV2O5 ECD and the role of V2O5 were investigated.

  5. A versatile SERS-based immunoassay for immunoglobulin detection using antigen-coated gold nanoparticles and malachite green-conjugated protein A/G

    Science.gov (United States)

    A surface enhanced Raman scattering (SERS) immunoassay for antibody detection in serum is described in the present work. The developed assay is conducted in solution and utilizes Au nanoparticles coated with the envelope (E) protein of West Nile Virus (WNV) as the SERS-active substrate and malachite...

  6. Reduced graphene oxide/δ-WO{sub 3} composites for volatile organic compounds sensing

    Energy Technology Data Exchange (ETDEWEB)

    Perfecto, Tarcisio Micheli; Zito, Cecilia de Almeida; Volanti, Diogo Paschoalini, E-mail: tarcisio93@hotmail.com [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), Sao Paulo, SP (Brazil)

    2016-07-01

    Full text: Metal oxide semiconductors (MOS) is a simple and low-cost alternative to detect volatile organic compounds (VOCs) with fast response and recovery time [1]. In this context, reduced graphene oxide (RGO) is used in order to achieve a superior metal oxides gas sensing performance [2]. Thus, we report the synthesis of RGO/δ-WO{sub 3} composites by microwave-assisted hydrothermal method and its application in VOCs detection. The composites were prepared in a single-step using a graphene oxide dispersion, tungsten salt, ammonium oxalate hydrate as morphological control agent, and HCl in aqueous medium. The mixture was sealed in an autoclave and irradiated by microwave (800W) at 140 °C for 10 minutes. Then the sample was heating treatment at 400 °C for 1 hour. δ-WO{sub 3} single phase was also prepared by the same process without graphene oxide. The XRD results indicated the successful formation of triclinic phase of WO{sub 3} for both samples. FEG-SEM images showed the δ-WO{sub 3} nanoplates formation that are agglomerated and become more disperse and with irregular shape in RGO/δ-WO{sub 3} composite. TEM analysis revealed the interaction between RGO and δ-WO{sub 3} particles. The preliminary gas sensing results showed that increasing the operation temperature, more sensitive the composite RGO/δ-WO{sub 3} was toward the ethanol, methanol, acetone, toluene and benzene. So far, the highest response observed was to acetone at 300 °C. The response of RGO/δ-WO{sub 3} to 5, 10, 50, 100 and 200 ppm of acetone was 1.08, 1.12, 1.42, 1.75, and 1.99, respectively. We expect that increasing the operating temperature, more sensitive the material will become, since reports shows that WO{sub 3} sensors exhibit higher responses at higher temperatures [3]. Acknowledgments: The authors acknowledge FAPESP grants: 16/04371-1, 15/04306-2 and 14/17343-0. Refs.: [1] Jiang, D.;et al. RSC Adv. 2015, 5 (49), 39442-39448. [2] Jie, X.; et al. Sensors Actuators B Chem. 2015, 220

  7. A comparative study for adsorption of lysozyme from aqueous samples onto Fe3O4 magnetic nanoparticles using different ionic liquids as modifier.

    Science.gov (United States)

    Kamran, Sedigheh; Absalan, Ghodratollah; Asadi, Mozaffar

    2015-12-01

    In this paper, nanoparticles of Fe3O4 as well as their modified forms with different ionic liquids (IL-Fe3O4) were prepared and used for adsorption of lysozyme. The mean size and the surface morphology of the nanoparticles were characterized by TEM, XRD and FTIR techniques. Adsorption studies of lysozyme were performed under different experimental conditions in batch system on different modified magnetic nanoparticles such as, lysozyme concentration, pH of the solution, and contact time. Experimental results were obtained under the optimum operational conditions of pH 9.0 and a contact time of 10 min when initial protein concentrations of 0.05-2.0 mg mL(-1) were used. The isotherm evaluations revealed that the Langmuir model attained better fits to the equilibrium data than the Freundlich model. The maximum obtained adsorption capacities were 370.4, 400.0 500.0 and 526.3 mg of lysozyme for adsorption onto Fe3O4 and modified magnetic nanoparticles by [C4MIM][Br], [C6MIM][Br] and [C8MIM][Br] per gram of adsorbent, respectively. The Langmuir adsorption constants were 0.004, 0.019, 0.024 and 0.012 L mg(-1) for adsorptions of lysozyme onto Fe3O4 and modified magnetic nanoparticles by [C4MIM][Br], [C6MIM][Br] and [C8MIM][Br], respectively. The adsorption capacity of lysozyme was found to be dependent on its chemical structure, pH of the solution, temperature and type of ionic liquid as modifier. The applicability of two kinetic models including pseudo-first order and pseudo-second order model was estimated. Furthermore, the thermodynamic parameters were calculated. Protein could desorb from IL-Fe3O4 nanoparticles by using NaCl solution at pH 9.5 and was reused.

  8. Intrinsic Defects and H Doping in WO3

    KAUST Repository

    Zhu, Jiajie

    2017-01-18

    WO3 is widely used as industrial catalyst. Intrinsic and/or extrinsic defects can tune the electronic properties and extend applications to gas sensors and optoelectonics. However, H doping is a challenge to WO3, the relevant mechanisms being hardly understood. In this context, we investigate intrinsic defects and H doping by density functional theory and experiments. Formation energies are calculated to determine the lowest energy defect states. O vacancies turn out to be stable in O-poor environment, in agreement with X-ray photoelectron spectroscopy, and O-H bond formation of H interstitial defects is predicted and confirmed by Fourier transform infrared spectroscopy.

  9. Understanding the Potential of WO3 Based Sensors for Breath Analysis

    Science.gov (United States)

    Staerz, Anna; Weimar, Udo; Barsan, Nicolae

    2016-01-01

    Tungsten trioxide is the second most commonly used semiconducting metal oxide in gas sensors. Semiconducting metal oxide (SMOX)-based sensors are small, robust, inexpensive and sensitive, making them highly attractive for handheld portable medical diagnostic detectors. WO3 is reported to show high sensor responses to several biomarkers found in breath, e.g., acetone, ammonia, carbon monoxide, hydrogen sulfide, toluene, and nitric oxide. Modern material science allows WO3 samples to be tailored to address certain sensing needs. Utilizing recent advances in breath sampling it will be possible in the future to test WO3-based sensors in application conditions and to compare the sensing results to those obtained using more expensive analytical methods. PMID:27801881

  10. Preparation of ultra-thin and high-quality WO{sub 3} compact layers and comparision of WO{sub 3} and TiO{sub 2} compact layer thickness in planar perovskite solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jincheng; Shi, Chengwu, E-mail: shicw506@foxmail.com; Chen, Junjun; Wang, Yanqing; Li, Mingqian

    2016-06-15

    In this paper, the ultra-thin and high-quality WO{sub 3} compact layers were successfully prepared by spin-coating-pyrolysis method using the tungsten isopropoxide solution in isopropanol. The influence of WO{sub 3} and TiO{sub 2} compact layer thickness on the photovoltaic performance of planar perovskite solar cells was systematically compared, and the interface charge transfer and recombination in planar perovskite solar cells with TiO{sub 2} compact layer was analyzed by electrochemical impedance spectroscopy. The results revealed that the optimum thickness of WO{sub 3} and TiO{sub 2} compact layer was 15 nm and 60 nm. The planar perovskite solar cell with 15 nm WO{sub 3} compact layer gave a 9.69% average and 10.14% maximum photoelectric conversion efficiency, whereas the planar perovskite solar cell with 60 nm TiO{sub 2} compact layer achieved a 11.79% average and 12.64% maximum photoelectric conversion efficiency. - Graphical abstract: The planar perovskite solar cell with 15 nm WO{sub 3} compact layer gave a 9.69% average and 10.14% maximum photoelectric conversion efficiency, whereas the planar perovskite solar cell with 60 nm TiO{sub 2} compact layer achieved a 11.79% average and 12.64% maximum photoelectric conversion efficiency. Display Omitted - Highlights: • Preparation of ultra-thin and high-quality WO{sub 3} compact layers. • Perovskite solar cell with 15 nm-thick WO{sub 3} compact layer achieved PCE of 10.14%. • Perovskite solar cell with 60 nm-thick TiO{sub 2} compact layer achieved PCE of 12.64%.

  11. Ag-Modified In2O3 Nanoparticles for Highly Sensitive and Selective Ethanol Alarming

    Directory of Open Access Journals (Sweden)

    Jinxiao Wang

    2017-09-01

    Full Text Available Pure In2O3 nanoparticles are prepared by a facile precipitation method and are further modified by Ag. The synthesized samples are characterized by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, Raman and UV-Vis spectra. The results show the successful heterojunction formation between Ag and In2O3. Gas sensing property measurements show that the 5 mol % Ag-modified In2O3 sensor has the response of 67 to 50 ppm ethanol, and fast response and recovery time of 22.3 and 11.7 s. The response is over one magnitude higher than that of pure In2O3, which can be attributed to the enhanced catalytic activity of Ag-modified In2O3 as compared with the pure one. The mechanism of the gas sensor can be explained by the spillover effect of Ag, which enhances the oxygen adsorption onto the surface of In2O3 and thus give rise to the higher activity and larger surface barrier height.

  12. Insight into synergistically enhanced adsorption and visible light photocatalytic performance of Z-scheme heterojunction of SrTiO{sub 3}(La,Cr)-decorated WO{sub 3} nanosheets

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xin; Jiang, Junzhe; Jia, Yushuai, E-mail: ysjia@jxnu.edu.cn; Qiu, Jinmin; Xia, Tonglin; Zhang, Yuhong; Li, Yuqin; Chen, Xiangshu, E-mail: cxs66cn@jxnu.edu.cn

    2017-08-01

    Highlights: • Fabrication of SrTiO{sub 3}(La,Cr)/WO{sub 3} heterojunction with well-defined morphology. • Synergistic effect of adsorption and photocatalytic elimination for methylene blue. • Adsorption kinetics and isotherm were investigated in detail. • Negative zeta potential and large surface area result in high adsorption capacity. • A novel Z-scheme mechanism for the enhanced photocatalytic activity is proposed. - Abstract: The efficient treatment of dye wastewater has been a hot topic of environment field. The integration of adsorption and photocatalytic degradation via fabrication of bi-component heterojunction photocatalyst is considered as a facile and effective strategy to enhance the dye elimination efficiency. In this report, a Z-scheme heterojunction material, SrTiO{sub 3}(La,Cr)/WO{sub 3} with bifunction of adsorption and photocatalysis was successfully synthesized for efficient removal of methylene blue (MB) under visible light irradiation. The morphology and microstructure characterization demonstrates that the SrTiO{sub 3}(La,Cr) nanoparticles are uniformly decorated on the WO{sub 3} nanosheets, forming an intimate heterojunction interface. MB degradation results indicate that the removal efficiency by the synergistic adsorption-photocatalysis process is greatly improved compared to pure WO{sub 3} and SrTiO{sub 3}(La,Cr) with the adsorption and photocatalytic activity closely related to the composition of the material. The possible mechanism for the enhanced photocatalytic activity could be ascribed to the formation of a Z-scheme heterojunction system based on active species trapping experiments. Furthermore, the investigations of adsorption kinetics and isotherm show that the adsorption process follows pseudo-second-order kinetic model and Langmuir isotherm, respectively. Due to the synergistic advantages of negative zeta potential, large surface area and accelerated separation of photogenerated carriers driven by Z

  13. Gd_2O_3 nanoparticles stabilized by hydrothermally modified dextrose for positive contrast magnetic resonance imaging

    International Nuclear Information System (INIS)

    Babić-Stojić, Branka; Jokanović, Vukoman; Milivojević, Dušan; Požek, Miroslav; Jagličić, Zvonko; Makovec, Darko; Arsikin, Katarina; Paunović, Verica

    2016-01-01

    Gd_2O_3 nanoparticles of a few nm in size and their agglomerates dispersed in dextrose derived polymer template were synthesized by hydrothermal treatment. The produced nanosized material was investigated by TEM, FTIR spectroscopy, SQUID measurements and NMR relaxometry. Biological evaluation of this material was done by crystal violet and MTT assays to determine the cell viability. Longitudinal and transverse NMR relaxivities of water diluted Gd_2O_3 nanoparticle dispersions measured at the magnetic field of 1.5 T, estimated to be r_1(Gd_2O_3)=9.6 s"−"1 mM"−"1 in the Gd concentration range 0.1–30 mM and r_2(Gd_2O_3)=17.7 s"−"1 mM"−"1 in the lower concentration range 0.1–0.8 mM, are significantly higher than the corresponding relaxivities measured for the standard contrast agent r_1(Gd-DTPA)=4.1 s"−"1 mM"−"1 and r_2(Gd-DTPA)=5.1 s"−"1 mM"−"1. The ratio of the two relaxivities for Gd_2O_3 nanoparticles r_2/r_1=1.8 is suitable for T_1-weighted imaging. Good MRI signal intensities of the water diluted Gd_2O_3 nanoparticle dispersions were recorded at lower Gd concentrations 0.2–0.8 mM. The Gd_2O_3 samples did not exert any significant cytotoxic effects at Gd concentrations of 0.2 mM and below. These properties of the produced Gd_2O_3 nanoparticles in hydrothermally modified dextrose make them promising for potential application in MRI for the design of a positive MRI contrast agent. - Highlights: • Gd_2O_3 nanoparticles (NPs) were stabilized by hydrothermally modified dextrose. • Magnetic moment per Gd"3"+ ion in the Gd_2O_3 NPs is much lower than that in the bulk. • The ratio r_2/r_1=1.8 for Gd_2O_3 NPs dispersions is favorable for T_1-weighted MRI. • Gd_2O_3 NPs dispersions had good MRI signal intensity just at lower Gd concentrations. • Gd concentrations of 0.2 mM and below in the Gd_2O_3 NPs dispersions were not toxic.

  14. Increased cellular uptake of peptide-modified PEGylated gold nanoparticles.

    Science.gov (United States)

    He, Bo; Yang, Dan; Qin, Mengmeng; Zhang, Yuan; He, Bing; Dai, Wenbing; Wang, Xueqing; Zhang, Qiang; Zhang, Hua; Yin, Changcheng

    2017-12-09

    Gold nanoparticles are promising drug delivery vehicles for nucleic acids, small molecules, and proteins, allowing various modifications on the particle surface. However, the instability and low bioavailability of gold nanoparticles compromise their clinical application. Here, we functionalized gold nanoparticles with CPP fragments (CALNNPFVYLI, CALRRRRRRRR) through sulfhydryl PEG to increase their stability and bioavailability. The resulting gold nanoparticles were characterized with transmission electron microscopy (TEM), dynamic light scattering (DLS), UV-visible spectrometry and X-ray photoelectron spectroscopy (XPS), and the stability in biological solutions was evaluated. Comparing to PEGylated gold nanoparticles, CPP (CALNNPFVYLI, CALRRRRRRRR)-modified gold nanoparticles showed 46 folds increase in cellular uptake in A549 and B16 cell lines, as evidenced by the inductively coupled plasma atomic emission spectroscopy (ICP-AES). The interactions between gold nanoparticles and liposomes indicated CPP-modified gold nanoparticles bind to cell membrane more effectively than PEGylated gold nanoparticles. Surface plasmon resonance (SPR) was used to measure interactions between nanoparticles and the membrane. TEM and uptake inhibitor experiments indicated that the cellular entry of gold nanoparticles was mediated by clathrin and macropinocytosis. Other energy independent endocytosis pathways were also identified. Our work revealed a new strategy to modify gold nanoparticles with CPP and illustrated the cellular uptake pathway of CPP-modified gold nanoparticles. Copyright © 2017 Elsevier Inc. All rights reserved.

  15. Charge doping and large lattice expansion in oxygen-deficient heteroepitaxial WO3

    Science.gov (United States)

    Mattoni, Giordano; Filippetti, Alessio; Manca, Nicola; Zubko, Pavlo; Caviglia, Andrea D.

    2018-05-01

    Tungsten trioxide (WO3) is a versatile material with widespread applications ranging from electrochromics and optoelectronics to water splitting and catalysis of chemical reactions. For technological applications, thin films of WO3 are particularly appealing, taking advantage from a high surface-to-volume ratio and tunable physical properties. However, the growth of stoichiometric crystalline thin films is challenging because the deposition conditions are very sensitive to the formation of oxygen vacancies. In this paper, we show how background oxygen pressure during pulsed laser deposition can be used to tune the structural and electronic properties of WO3 thin films. By performing x-ray diffraction and low-temperature electrical transport measurements, we find changes in the WO3 lattice volume of up to 10% concomitantly with a resistivity drop of more than five orders of magnitude at room temperature as a function of increased oxygen deficiency. We use advanced ab initio calculations to describe in detail the properties of the oxygen vacancy defect states and their evolution in terms of excess charge concentration. Our results depict an intriguing scenario where structural, electronic, optical, and transport properties of WO3 single-crystal thin films can all be purposely tuned by controlling the oxygen vacancy formation during growth.

  16. Study on photocurrent of bilayers photoanodes using different combination of WO{sub 3} and Fe{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Memar, Amir; Daud, Wan Ramli Wan; Eftekhari, Ehsan; Minggu, Lorna Jeffery [Institute of Fuel Cell, University Kebangsaan Malaysia, 43600 Bangi, Selangor (Malaysia); Hosseini, Soraya [Department Chemical and Environmental Engineering, University Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia)

    2010-08-15

    Bilayer photoanodes were prepared onto glass substrates (FTO) in order to improve generated photocurrents using UV-vis light by water splitting process. A comparative study of photocatalytic was performed over the films surface using Fe{sub 2}O{sub 3,} WO{sub 3} and mixture of bicomponents (Fe{sub 2}O{sub 3}:WO{sub 3}). Different types of films were prepared using Fe{sub 2}O{sub 3,} WO{sub 3} and bicomponents (mixture) on FTO substrates. The films were grown by sol gel method with the PEG-300 as the structure-directing agent. The photo-generated of the samples were determined by measuring the currents and voltages under illumination of UV-vis light. The morphology, structure and related composition distribution of the films have been characterized by SEM, XRD and EDX respectively. Photocurrent measurements indicated surface roughness as the effective parameter in this study. The deposited surfaces by bicomponents or mixture are flat without any feature on the surface while the deposited surfaces by WO{sub 3} appears rough surface as small round (egg-shaped particles) and cauliflower-like. The surface deposited by Fe{sub 2}O{sub 3} show rough no as well as WO{sub 3} surface. The deposited surfaces by WO{sub 3} reveal the higher value of photocurrent measurement due to surface roughness. Indeed, the roughness can be effective in increasing contact surface area between film and electrolyte and diffuse reflection (light scattering effect). The solution (Fe{sub 2}O{sub 3}:WO{sub 3}) shows the low photocurrent value in compare to WO{sub 3} and Fe{sub 2}O{sub 3} hat it may be due to decomposition the compound at 450 {+-} 1 C to iron-tungstate Fe{sub 2}(WO{sub 4}){sub 3}. (author)

  17. Physical properties characterization of WO{sub 3} films grown by hot-filament metal oxide deposition

    Energy Technology Data Exchange (ETDEWEB)

    Diaz-Reyes, J., E-mail: jdiazr2001@yahoo.com [Centro de Investigacion en Biotecnologia Aplicada del Instituto Politecnico Nacional, Ex-Hacienda de San Juan Molino, Km. 1.5, Tepetitla, Tlaxcala, 90700 (Mexico); Delgado-Macuil, R.J. [Centro de Investigacion en Biotecnologia Aplicada del Instituto Politecnico Nacional, Ex-Hacienda de San Juan Molino, Km. 1.5, Tepetitla, Tlaxcala, 90700 (Mexico); Dorantes-Garcia, V. [Preparatoria ' Simon Bolivar' de la Benemerita Universidad Autonoma de Puebla, 4 Oriente 408, Col. Centro, Atlixco, Puebla, C. P. 74200 (Mexico); Perez-Benitez, A. [Facultad de Ciencias Quimicas de la Benemerita Universidad Autonoma Puebla, 14 Sur y Av. San Claudio, Col. San Manuel, Puebla, Puebla, C. P. 72570 (Mexico); Balderas-Lopez, J.A. [Unidad Profesional Interdisciplinaria de Biotecnologia del Instituto Politecnico Nacional, Avenida Acueducto S/N, Col. Barrio la Laguna, Ticoman, Del. Gustavo A. Madero, Mexico, D.F. 07340 (Mexico); Ariza-Ortega, J.A. [Centro de Investigacion en Biotecnologia Aplicada del Instituto Politecnico Nacional, Ex-Hacienda de San Juan Molino, Km. 1.5, Tepetitla, Tlaxcala, 90700 (Mexico)

    2010-10-25

    WO{sub 3} is grown by hot-filament metal oxide deposition (HFMOD) technique under atmospheric pressure and an oxygen atmosphere. By X-ray diffraction obtains that WO{sub 3} presents mainly monoclinic crystalline phase. The chemical stoichiometry is obtained by X-ray Photoelectron Spectroscopy (XPS). The IR spectrum of the as-grown WO{sub 3} presents broad peaks in the range of 1100 to 3600 cm{sup -1}. A broad band in the 2200 to 3600 cm{sup -1} region and the peaks sited at 1645 and 1432 cm{sup -1} are well resolved, which are originated from moisture and are assigned to {nu}(OH) and {delta}(OH) modes of adsorbed water and the corresponding tungsten oxide vibrations are in infrared region from 400 to 1453 cm{sup -1} and around 3492 cm{sup -1}, which correspond to tungsten-oxygen (W-O) stretching, bending and lattice modes. The Raman spectrum shows intense peaks at 801, 710, 262 and 61 cm{sup -1} that are typical Raman peaks of crystalline WO{sub 3} (m-phase) that correspond to stretching vibrations of the bridging oxygen, which are assigned to W-O stretching ({nu}) and W-O bending ({delta}) modes, respectively. By transmittance measurements obtains that the WO{sub 3} band gap can be varied from 2.92 to 3.13 eV in the investigated annealing temperature range.

  18. Tungsten oxides. I. Effects of oxygen vacancies and doping on electronic and optical properties of different phases of WO3

    Science.gov (United States)

    Migas, D. B.; Shaposhnikov, V. L.; Rodin, V. N.; Borisenko, V. E.

    2010-11-01

    In this part we present results of our ab initio calculations indicating that dispersion of the bands near the gap region for different phases of WO3 (namely, ɛ-WO3, δ-WO3, γ-WO3, β-WO3, orth-WO3, α-WO3, and hex-WO3) is rather close. The rapid increase in the absorption coefficient starts at the lower energy range for α-WO3 and hex-WO3 than for the other phases in accordance with the calculated band gaps. An oxygen vacancy has turned out to decrease the gap by 0.50 eV and to shift the absorption coefficient to the lower energy range in the room temperature γ-WO3 phase. We have also traced changes caused by molybdenum and sulfur doping of γ-WO3. Only sulfur doped γ-WO3 has been revealed to display the formation of the impurity band along with a sizable reduction in the gap and the shift in the absorption coefficient to the lower energy range.

  19. Synthesis and magnetic properties of prussian blue modified Fe nanoparticles

    International Nuclear Information System (INIS)

    Arun, T.; Prakash, K.; Justin Joseyphus, R.

    2013-01-01

    Fe nanoparticles are prepared using a unique polyol process and modified with prussian blue (PB) at various concentrations. The presence of PB in the Fe nanoparticles are confirmed from thermal, Fourier transform infrared spectroscopy and electron microscopic analyses. The prussian blue existed on ;the surface of the nanoparticles when the concentration is 200 μM and in excess with 1000 μM. ;Fe nanoparticles are reduced in size using Pt as nucleating agent and modified with the optimum concentration of PB. The saturation magnetization decreases with the concentration of PB whereas the coercivity is influenced by the size of the Fe nanoparticles. The presence of oxide layer in Fe nanoparticles helps in the surface modification with PB. The Fe nanoparticles of particle size 53 nm modified with 200 μM of PB showed a saturation magnetization of 110 emu/g. The magnetic properties suggest that the PB modified Fe nanoparticles are better candidates for detoxification applications. - Highlights: • Fe nanoparticles surface modified with prussian blue (PB) were synthesized. • Optimum PB concentration on size reduced Fe showed better magnetic properties. • Coercivity decreased with increasing concentration of PB. • Fe-PB nanoparticles could be used for detoxification applications

  20. Optimization, yield studies and morphology of WO3 nano-wires synthesized by laser pyrolysis in C2H2 and O2 ambients—validation of a new growth mechanism

    CSIR Research Space (South Africa)

    Mwakikunga, BW

    2008-10-01

    Full Text Available Laser pyrolysis has been used to synthesize WO3 nanostructures. Spherical nano-particles were obtained when acetylene was used to carry the precursor droplet, whereas thin films were obtained at high flow-rates of oxygen carrier gas. In both...

  1. Photocatalytic activity of Bi{sub 2}WO{sub 6}/Bi{sub 2}S{sub 3} heterojunctions: the facilitation of exposed facets of Bi{sub 2}WO{sub 6} substrate

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Long [School of Chemistry and Chemical Engineering, Yulin University, Shaanxi Key Laboratory of Low Metamorphic Coal Clean Utilization, Yulin 71900 (China); School of Chemistry and Chemical Engineering, Yan’an University, Shaanxi Key Laboratory of Chemical Reaction Engineering, Yan’an 716000 (China); Wang, Yufei [School of Chemistry and Chemical Engineering, Yulin University, Shaanxi Key Laboratory of Low Metamorphic Coal Clean Utilization, Yulin 71900 (China); Shen, Huidong; Zhang, Yu [School of Chemistry and Chemical Engineering, Yan’an University, Shaanxi Key Laboratory of Chemical Reaction Engineering, Yan’an 716000 (China); Li, Jian [School of Chemistry and Chemical Engineering, Yulin University, Shaanxi Key Laboratory of Low Metamorphic Coal Clean Utilization, Yulin 71900 (China); Wang, Danjun, E-mail: yulyanlong@aliyun.com [School of Chemistry and Chemical Engineering, Yan’an University, Shaanxi Key Laboratory of Chemical Reaction Engineering, Yan’an 716000 (China)

    2017-01-30

    Highlights: • Bi{sub 2}S{sub 3}/Bi{sub 2}WO{sub 6} hybrids with exposed (020) Bi{sub 2}WO{sub 6} facets have been synthesized. • X-ray photoelectron spectroscopy reveals that a small amount of Bi{sub 2}S{sub 3} was formed. • The enhanced photoactivity of hybrids is due to heterojunction and (020) facets. • A possible photocatalytic degradation mechanism is proposed. - Abstract: Bi{sub 2}S{sub 3}/Bi{sub 2}WO{sub 6} hybrid architectures with exposed (020) Bi{sub 2}WO{sub 6} facets have been synthesized via a controlled anion exchange approach. X-ray photoelectron spectroscopy (XPS) reveals that a small amount of Bi{sub 2}S{sub 3} was formed on the surface of Bi{sub 2}WO{sub 6} during the anion exchange process, thus leading to the transformation from the Bi{sub 2}WO{sub 6} to Bi{sub 2}S{sub 3}/Bi{sub 2}WO{sub 6}. A rhodamine B (RhB) aqueous solution was chosen as model organic pollutants to evaluate the photocatalytic activities of the Bi{sub 2}S{sub 3}/Bi{sub 2}WO{sub 6} catalysts. Under visible light irradiation, the Bi{sub 2}S{sub 3}/Bi{sub 2}WO{sub 6}-TAA displayed the excellent visible light photoactivities compared with pure Bi{sub 2}S{sub 3}, Bi{sub 2}WO{sub 6} and other composite photocatalysts. The efficient photocatalytic activity of the Bi{sub 2}S{sub 3}/Bi{sub 2}WO{sub 6}-TAA composite microspheres was ascribed to the constructed heterojunctions and the inner electric field caused by the exposed (020) Bi{sub 2}WO{sub 6} facets. Active species trapping experiments revealed that h{sup +} and O{sub 2}·{sup −} are the main active species in the photocatalytic process. Furthermore, the as-obtained photocatalysts showed good photocatalytic activity after four recycles. The results presented in this study provide a new concept for the rational design and development of highly efficient photocatalysts.

  2. Acrylonitrile butadiene rubber (NBR)/manganous tungstate (MnWO4) nanocomposites: Characterization, mechanical and electrical properties

    Science.gov (United States)

    Ramesan, M. T.; Abdu Raheem V., P.; Jayakrishnan, P.; Pradyumnan, P. P.

    2014-10-01

    Nanocomposites of NBR with manganous-tungstate nanoparticles were prepared through vulcanization process. The extent of interaction of nanoparticles with the polymer was studied by FTIR, SEM, XRD, TGA and AC conductivity. FTIR and XRD ascertain the interaction of NBR with MnWO4 nanoparticles. SEM analysis established that the nanopartilces were well dispersed in the macromolecular chain of NBR. The mechanical properties of the nanocomposites were studied as a function of filler loading. The nanocomposites exhibited enhanced thermal stability as seen in TGA. Conductivity and dielectric properties of nanocomposites increase with increase in concentration of MnWO4 nanoparticles (7phr) and thereafter the value decreases.

  3. Subsolidus Phase Relations of the CaO-WO3-CuO System at 800 °C in Air

    DEFF Research Database (Denmark)

    Grivel, J. -C.

    2012-01-01

    The subsolidus phase relations of the CaO-WO3-CuO system were investigated in air. The samples were equilibrated at 800 degrees C. Under these conditions, five binary oxide phases are stable: Ca2CuO3, Cu3WO6, CuWO4, CaWO4 and Ca3WO6. The pseudo-ternary section is characterised by 6 three...

  4. Conductive surface modification of cauliflower-like WO{sub 3} and its electrochemical properties for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Sukeun, E-mail: skyoon@kongju.ac.kr [Division of Advanced Materials Engineering, Kongju National University, Chungnam 330-717 (Korea, Republic of); Woo, Sang-Gil [Advanced Batteries Research Center, Korea Electronics Technology Institute, Gyeonggi 463-816 (Korea, Republic of); Jung, Kyu-Nam [Energy Efficiency and Materials Research Division, Korea Institute of Energy Research, Daejeon 305-343 (Korea, Republic of); Song, Huesup, E-mail: hssong@kongju.ac.kr [Division of Advanced Materials Engineering, Kongju National University, Chungnam 330-717 (Korea, Republic of)

    2014-11-15

    Highlights: • Synthesis of cauliflower-like carbon-decorated WO{sub 3}. • Superior cyclability and rate capability for cauliflower-like carbon-decorated WO{sub 3}. • Electrochemical reaction behavior of cauliflower-like carbon-decorated WO{sub 3} with lithium. • In-situ XRD analysis during the first discharge–charge shows a complex reaction of intercalation and conversion of WO{sub 3}. - Abstract: Cauliflower-like WO{sub 3} was synthesized by a hydrothermal reaction without a surfactant, followed by firing, and was investigated as an anode material for lithium-ion battery applications. The scanning electron microscope (SEM) and transmission electron microscope (TEM) characterization indicated that WO{sub 3} nanorods had an aggregation framework and built a cauliflower morphology. With the objective of understanding the charge–discharge process within a voltage range of 0–3 V vs. Li{sup +}/Li, in situ X-ray diffraction was used and a complex reaction of intercalation and conversion of WO{sub 3} was revealed for the first time. The cauliflower-like WO{sub 3} after being decorated with carbon provides a high gravimetric capacity of >635 mA h/g (Li{sub 5.5}WO{sub 3}) with good cycling and a high rate capability when used as an anode in lithium-ion batteries. Based on our studies, we attribute the high electrochemical performance to the nanoscopic WO{sub 3} particles and a conductive carbon layer, which makes them a potential candidate for lithium-ion batteries.

  5. In situ synthesis of Bi2S3 sensitized WO3 nanoplate arrays with less interfacial defects and enhanced photoelectrochemical performance

    Science.gov (United States)

    Liu, Canjun; Yang, Yahui; Li, Wenzhang; Li, Jie; Li, Yaomin; Chen, Qiyuan

    2016-03-01

    In this study, Bi2S3 sensitive layer has been grown on the surface of WO3 nanoplate arrays via an in situ approach. The characterization of samples were carried out using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and ultraviolet-visible absorption spectroscopy (UV-vis). The results show that the Bi2S3 layer is uniformly formed on the surface of WO3 nanoplates and less interfacial defects were observed in the interface between the Bi2S3 and WO3. More importantly, the Bi2S3/WO3 films as photoanodes for photoelectrochemical (PEC) cells display the enhanced PEC performance compared with the Bi2S3/WO3 films prepared by a sequential ionic layer adsorption reaction (SILAR) method. In order to understand the reason for the enhanced PEC properties, the electron transport properties of the photoelectrodes were studied by using the transient photocurrent spectroscopy and intensity modulated photocurrent spectroscopy (IMPS). The Bi2S3/WO3 films prepared via an in situ approach have a greater transient time constant and higher electron transit rate. This is most likely due to less interfacial defects for the Bi2S3/WO3 films prepared via an in situ approach, resulting in a lower resistance and faster carrier transport in the interface between WO3 and Bi2S3.

  6. Preparation of Er3+:Y3Al5O12/WO3-KNbO3 composite and application in treatment of methamphetamine under ultrasonic irradiation.

    Science.gov (United States)

    Zhang, Hongbo; Huang, Yingying; Li, Guanshu; Wang, Guowei; Fang, Dawei; Song, Youtao; Wang, Jun

    2017-03-01

    Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 composite powder as an effective sonocatalyst was prepared via collosol-gelling-hydrothermal and high-temperature calcination methods. The textures of materials were observed by X-ray diffractometer (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). In order to estimate the sonocatalytic activity of Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 composite powder, the sonocatalytic degradation of methamphetamine (MAPA) was performed. Furthermore, the influences of mass ratio of WO 3 and KNbO 3 , ultrasonic irradiation time, catalyst addition amount, initial methamphetamine (MAPA) concentration and used times on the sonocatalytic degradation of methamphetamine (MAPA) caused by Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 composite powder were investigated by using gas chromatography. Under optimal conditions of 1.00g/L Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 addition amount and 10.00mg/L methamphetamine (MAPA) initial concentration, 68% of methamphetamine (MAPA) could be removed after 150min ultrasonic irradiation. The experimental results showed that the Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 as sonocatalyst displayed an excellent sonocatalytic activity in degradation of methamphetamine (MAPA) under ultrasonic irradiation. Copyright © 2016 Elsevier B.V. All rights reserved.

  7. Study of the tungsten bronze Ag0.01WO3 using positron annihilation method

    International Nuclear Information System (INIS)

    Dryzek, J.; Dryzek, E.; Placzek, A.

    1992-01-01

    The study of the positron annihilation and the Seebeck effect was performed on silver doped tungsten trioxide of composition Ag 0.01 WO 3 and the tungsten trioxide phase: WO 2.90 (W 20 O 58 ). Both methods point out that there are some clusters of Ag + ions in the first compound and oxygen vacancies in the second case. The clusters have some internal substructure. The measurements of the Seebeck effect showed that Ag 0.01 WO 3 is normal n-type semiconductor whereas WO 2.90 exhibits metal-like properties

  8. Investigation of optical properties and the photocatalytic activity of synthesized YbYO4 nanoparticles and YbVO4/NiWO4 nanocomposites by polymeric capping agents

    Science.gov (United States)

    Pourmasoud, Saeid; Sobhani-Nasab, Ali; Behpour, Mohsen; Rahimi-Nasrabadi, Mehdi; Ahmadi, Farhad

    2018-04-01

    YbVO4 nanoparticles YbVO4/NiWO4 nanocomposites were synthesized by simple and new method. The effect of various polymeric capping agents such as Tween 80, Tween 20 and PEG on the shape and size of YbVO4/NiWO4 nanocomposites were investigated. YbVO4/NiWO4 nanocomposites were analyzed through some techniques including, X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy, vibrating sample magnetometer (VSM), thermogravimetry differential thermal analysis (TG-DTA), transmission electron microscopy (TEM), field emission electron microscopy (FESEM), ultraviolet-visible spectroscopy (UV-Vis), and energy-dispersive X-ray spectroscopy (EDX). This attempt is the first study on the photocatalytic performance of the YbVO4/NiWO4 nanocomposites in various conditions such as size of particles and kind of dyes (rhodamine B (Rh B), methylene blue (MB), methyl orange (MO), and phenol red (Ph R)), under visible light.

  9. Preparation and photoelectric properties of p-CaFe2O4/n-WO3 composites

    International Nuclear Information System (INIS)

    Wan, Ruiqin; Jia, Caihong; Zhang, Weifeng

    2012-01-01

    Highlights: ► Surface photovoltage spectroscopy investigation on p-CaFe 2 O 4 /n-WO 3 composites. ► The photovoltaic response is enhanced in p-CaFe 2 O 4 /n-WO 3 composites. ► The multielectron process and high rate of carrier migration in WO 3 . - Abstract: Composites of p-CaFe 2 O 4 /n-WO 3 are prepared via a sol–gel technique. Their structures and optical properties are characterized with X-ray diffraction, scanning electron microscopy and UV–vis absorption spectroscopy. The photoelectric characteristics are investigated by surface photovoltage spectroscopy combined with electric field induced surface photovoltage spectroscopy. The results indicate that CaFe 2 O 4 can well form a p–n type composite with WO 3 , and the intensity and spectral region of surface photovoltaic response for the composites are strongly dependent on the molar ratio of two components. The enhancement in photoelectric properties and the effective separation of photogenerated carriers could be attributed to the energy level matching between the two components, multielectron process and the high migration rate in WO 3 .

  10. Gas Sensor Based on 3-D WO3 Inverse Opal: Design and Applications

    Directory of Open Access Journals (Sweden)

    Ruiqing Xing

    2017-03-01

    Full Text Available A three-dimensional inverse opal (3DIO WO3 architecture has been synthesized via a simple sacrificial template method. Morphology features of the 3DIO were characterized by scanning electron microscope (SEM and its structure was characterized by X-ray diffraction (XRD. The shrinking ratio of the PMMA spheres was ~28.2% through measuring the distribution of the PMMA spheres and 3DIO WO3 center-to-center distance between the spheres and macropores, respectively. Beyond that, the 3DIO gas sensing properties were investigated systematically and the sensing mechanism of 3DIO WO3 was proposed. The results indicated that the response of the 3DIO sensor possessed excellent sensitivity to acetone gas, especially at trace levels. The 3DIO gas sensor response was ~7 to 5 ppm of acetone and could detect acetone low to 0.2 ppm effectively, which was in close proximity to the theoretical low detection limit of 0.14 ppm when Ra/Rg ≥ 1.2 was used as the criterion for reliable gas sensing. All in all, the obvious satisfaction of the gas-sensing properties was ascribed to the structure of the 3DIO, and the sensor could be a promising novel device in the future.

  11. Poly(methacrylic acid)-mediated morphosynthesis of PbWO4 micro-crystals

    International Nuclear Information System (INIS)

    Yu, J.G.; Zhao, X.F.; Liu, S.W.; Li, M.; Mann, S.; Ng, D.H.L.

    2007-01-01

    PbWO 4 crystals with various morphologies were fabricated via a facile poly(methacrylic acid)-mediated hydrothermal route. Novel microsized PbWO 4 single crystals with a needle-like shape as well as other morphologies, such as a fishbone, dendrite, sphere, spindle, ellipsoid, rod, and dumbbell with two dandelion-like heads, could be produced. The presence of PMAA, [Pb 2+ ]/[WO 4 2- ] molar ratio (R), and aging temperature played key roles in the formation of the PbWO 4 needle-like structures. Between temperatures of 60 to 150 C, the length and photoluminescence intensities of the PbWO 4 micro needles significantly increased with aging temperature, while the diameter did not change remarkably. Time-dependent experiments revealed that the formation of PbWO 4 microneedles involved an unusual growth process, involving nucleation, oriented assembly and controlled mesoscale restructuring of nanoparticle building blocks. (orig.)

  12. Incorporation of tantalum ions enhances the electrocatalytic activity of hexagonal WO3 nanowires for hydrogen evolution reaction

    International Nuclear Information System (INIS)

    Xie, Xiang; Mu, Wanjun; Li, Xingliang; Wei, Hongyuan; Jian, Yuan; Yu, Qianhong; Zhang, Rui; Lv, Kai; Tang, Hui; Luo, Shunzhong

    2014-01-01

    WO 3 has been identified as a promising candidate electrocatalyst for hydrogen evolution reaction (HER), because it can form a tungsten bronze (HxWO 3 ) which is highly electron and proton conducting. In this paper, we report that the electrocatalytic activity of WO 3 for HER can be enhanced by incorporation of tantalum ions (Ta 5+ ) into the lattice of WO 3 . The most active performance is achieved with the molar ratio of Ta/W being 0.01, which is two times more active than that of undoped WO 3 at an overpotential of -0.52 V. It is shown that incorporation of proper Ta 5+ into WO 3 can induce moderate defects and oxygen vacancies, as well as intercalate a higher amount of protons, which enhance the electron transfer and short the protons diffusion paths. These changes correlated positively with the enhanced catalytic HER activity. This study demonstrates, for the first time, that metal ions-doped WO 3 nanowires are promising electrocatalysts for HER

  13. Liquid phase deposition of WO3/TiO2 heterojunction films with high photoelectrocatalytic activity under visible light irradiation

    International Nuclear Information System (INIS)

    Zhang, Man; Yang, Changzhu; Pu, Wenhong; Tan, Yuanbin; Yang, Kun; Zhang, Jingdong

    2014-01-01

    Highlights: • Liquid phase deposition is developed for preparing WO 3 /TiO 2 heterojunction films. • TiO 2 film provides an excellent platform for WO 3 deposition. • WO 3 expands the absorption band edge of TiO 2 film to visible light region. • WO 3 /TiO 2 heterojunction film shows high photoelectrocatalytic activity. - ABSTRACT: The heterojunction films of WO 3 /TiO 2 were prepared by liquid phase deposition (LPD) method via two-step processes. The scanning electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopic analysis indicated that flower-like WO 3 film was successfully deposited on TiO 2 film with the LPD processes. The TiO 2 film provided an excellent platform for WO 3 deposition while WO 3 obviously expanded the absorption of TiO 2 film to visible light. As the result, the heterojunction film of WO 3 /TiO 2 exhibited higher photocurrent response to visible light illumination than pure TiO 2 or WO 3 film. The photoelectrocatalytic (PEC) activity of WO 3 /TiO 2 film was evaluated by degrading Rhodamin B (RhB) and 4-chlorophenol (4-CP) under visible light irradiation. The results showed that the LPD WO 3 /TiO 2 film possessed high PEC activity for efficient removal of various refractory organic pollutants

  14. Liposome-coated mesoporous silica nanoparticles loaded with L-cysteine for photoelectrochemical immunoassay of aflatoxin B1.

    Science.gov (United States)

    Lin, Youxiu; Zhou, Qian; Zeng, Yongyi; Tang, Dianping

    2018-06-02

    The authors describe a photoelectrochemical (PEC) immunoassay for determination of aflatoxin B 1 (AFB 1 ) in foodstuff. The competitive immunoreaction is carried out on a microplate coated with a capture antibody against AFB 1 using AFB 1 -bovine serum albumin (BSA)-liposome-coated mesoporous silica nanoparticles (MSN) loaded with L-cysteine as a support. The photocurrent is produced by a photoactive material consisting of cerium-doped Bi 2 MoO 6 . Initially, L-cysteine acting as the electron donor is gated in the pores by interaction between mesoporous silica and liposome. Thereafter, AFB 1 -BSA conjugates are covalently bound to the liposomes. Upon introduction of the analyte (AFB 1 ), the labeled AFB 1 -BSA complex competes with the analyte for the antibody deposited on the microplate. Accompanying with the immunocomplex, the liposomes on the MSNs are lysed upon addition of Triton X-100. This results in the opening of the pores and in a release of L-cysteine. Free cysteine then induces the electron-hole scavenger of the photoactive nanosheets to increase the photocurrent. The photocurrent (relative to background signal) increases with increasing AFB 1 concentration. Under optimum conditions, the photoactive nanosheets display good photoelectrochemical responses, and allow the detection of AFB 1 at a concentration as low as 0.1 pg·mL -1 within a linear response in the 0.3 pg·mL -1 to 10 ng·mL -1 concentration range. Accuracy was evaluated by analyzing naturally contaminated and spiked peanut samples by using a commercial AFB 1 ELISA kit as the reference, and well-matching results were obtained. Graphical abstract Schematic presentation of a photoelectrochemical immunoassay for AFB 1 . It is based on the use of Ce-doped Bi 2 MoO 6 nanosheets and of liposome-coated mesoporous silica nanoparticles loaded with L-cysteine.

  15. In situ loading of Ag{sub 2}WO{sub 4} on ultrathin g-C{sub 3}N{sub 4} nanosheets with highly enhanced photocatalytic performance

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yunfeng; Jin, Renxi; Fang, Xu; Yang, Yang; Yang, Man; Liu, Xianchun [Jilin Provincial Key Laboratory of Advanced Energy Materials, Department of Chemistry, Northeast Normal University, Changchun 130024 (China); Xing, Yan, E-mail: xingy202@nenu.edu.cn [Jilin Provincial Key Laboratory of Advanced Energy Materials, Department of Chemistry, Northeast Normal University, Changchun 130024 (China); Song, Shuyan [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

    2016-08-05

    Graphical abstract: Ultrathin g-C{sub 3}N{sub 4} nanosheets (g-C{sub 3}N{sub 4}−NS) with improved electron transport ability and large number of active sites are employed instead of bulk g-C{sub 3}N{sub 4} to prepare the Ag{sub 2}WO{sub 4}/g-C{sub 3}N{sub 4}−NS heterostructured photocatalysts, which exhibit remarkable photocatalytic activity for wastewater treatment. - Highlights: • Ag2WO4/g-C3N4-NS photocatalysts were obtained by a deposition-precipitation method. • Ag2WO4/g-C3N4-NS possess large surface areas and increased lifetime of charges. • Ag2WO4/g-C3N4-NS exhibit enhanced activity on degradation of RhB and MO. • The photocatalytic mechanism of the Ag2WO4/g-C3N4-NS system were investigated. - Abstract: The g-C{sub 3}N{sub 4} nanosheets (g-C{sub 3}N{sub 4}−NS) exhibit more excellent property than common bulk g-C{sub 3}N{sub 4} (g-C{sub 3}N{sub 4}-B) due to their large surface areas, improved electron transport ability and well dispersion in water. In this work, ultrathin g-C{sub 3}N{sub 4}−NS with a thickness of about 2.7 nm have been synthesized by a simple thermal exfoliation of bulk g-C{sub 3}N{sub 4}, and then Ag{sub 2}WO{sub 4} nanoparticles are in situ loaded on their surface to construct the Ag{sub 2}WO{sub 4}/g-C{sub 3}N{sub 4}−NS heterostructured photocatalysts. Due to their unique physicochemical properties, the as-prepared heterostructures possess a fast interfacial charge transfer and increased lifetime of photo-excited charge carriers, and exhibit much higher photocatalytic activity. Under visible light irradiation, the optimum photocatalytic activity of Ag{sub 2}WO{sub 4}/g-C{sub 3}N{sub 4}−NS composites is almost 53.6 and 26.5 times higher than that of pure g-C{sub 3}N{sub 4}-B and Ag{sub 2}WO{sub 4}/g-C{sub 3}N{sub 4}-B heterostructures towards the degradation of rhodamine B, respectively, and is almost 30.6 and 9.8 times higher towards the degradation of methyl orange, respectively. In addition, the natural sunlight

  16. Molecularly imprinted electrochemical sensor based on nickel nanoparticle-modified electrodes for phenobarbital determination

    International Nuclear Information System (INIS)

    Yu, Hui Cheng; Huang, Xue Yi; Lei, Fu Hou; Tan, Xue Cai; Wei, Yi Chun; Li, Hao

    2014-01-01

    Highlights: • Uniform Ni nanoparticles were synthesized. • A Ni nanoparticle-modified imprinted sensor was developed to detect phenobarbital. • The modified sensor exhibited high sensitivity for phenobarbital. • The electrochemical properties of the modified sensor were investigated. • The prepared sensor was applied to detect phenobarbital in fish samples. - Abstract: Uniform nickel nanoparticles were applied to improve the sensitivity of sensors for phenobarbital (PB) determination. A Ni nanoparticle-modified imprinted electrochemical sensor was developed by thermal polymerization with the use of methacrylic acid as the functional monomer and ethylene glycol maleic rosinate acrylate as the crosslinking agent. The chemical structures and morphologies of the imprinted films were characterized using Fourier transform infrared spectroscopy and scanning electron microscopy. The success of the fabrication of Ni nanoparticles, as well as the Ni nanoparticle-modified imprinted electrochemical sensor, was confirmed by the analytical results. The electrochemical properties of the modified molecularly imprinted and non-imprinted polymer sensors were investigated by cyclic voltammetry, differential pulse voltammetry, electrochemical impedance spectroscopy, and chronoamperometry. Results showed that the electrochemical properties of the molecularly imprinted sensor were remarkably different from those of the non-imprinted sensor. Linear responses of the imprinted sensor to PB were observed for concentrations ranging from 1.4 × 10 −7 mol L −1 to 1.3 × 10 −4 mol L −1 (r 2 = 0.9976), with a detection limit of 8.2 × 10 −9 mol L −1 (S/N = 3). The imprinted electrochemical sensor was used to determine PB in actual fish samples, in which average recoveries between 95.60% and 104.67% were achieved. The developed Ni nanoparticle-modified electrochemical sensor exhibited high sensitivity, high selectivity, and good recovery

  17. Structural properties of WO{sub 3} dependent of the annealing temperature deposited by hot-filament metal oxide deposition

    Energy Technology Data Exchange (ETDEWEB)

    Flores M, J. E. [Benemerita Universidad Autonoma de Puebla, Facultad de Ciencias de la Electronica, Av. San Claudio y 18 Sur, Ciudad Universitaria, Col. Jardines de San Manuel, 72570 Puebla (Mexico); Diaz R, J. [IPN, Centro de Investigacion en Biotecnologia Aplicada, Ex-Hacienda de San Molino Km 1.5 Tepetitla, 90700 Tlaxcala (Mexico); Balderas L, J. A., E-mail: eflores@ece.buap.mx [IPN, Unidad Profesional Interdisciplinaria de Biotecnologia, Av. Acueducto s/n, Col. Barrio la Laguna, 07340 Mexico D. F. (Mexico)

    2012-07-01

    In this work presents a study of the effect of the annealing temperature on structural and optical properties of WO{sub 3} that has been grown by hot-filament metal oxide deposition. The chemical stoichiometry was determined by X-ray photoelectron spectroscopy. By X-ray diffraction obtained that the as-deposited WO{sub 3} films present mainly monoclinic crystalline phase. WO{sub 3} optical band gap energy can be varied from 2.92 to 3.15 eV obtained by transmittance measurements by annealing WO{sub 3} from 100 to 500 C. The Raman spectrum of the as-deposited WO{sub 3} film shows four intense peaks that are typical Raman peaks of crystalline WO{sub 3} (m-phase) that corresponds to the stretching vibrations of the bridging oxygen that are assigned to W-O stretching ({upsilon}) and W-O bending ({delta}) modes, respectively, which enhanced and increased their intensity with the annealing temperature. (Author)

  18. Ultrathin Bi2WO6 nanosheet decorated with Pt nanoparticles for efficient formaldehyde removal at room temperature

    Science.gov (United States)

    Sun, Dong; Le, Yao; Jiang, Chuanjia; Cheng, Bei

    2018-05-01

    Two-dimensional (2D) ultrathin bismuth tungstate (Bi2WO6) nanosheets (BWO-NS) with a thickness of approximately 4.0 nm were synthesized by a one-step hydrothermal method, and decorated with platinum (Pt) nanoparticles (NPs) via an impregnation/borohydride-reduction approach. The as-prepared ultrathin Pt-BWO-NS exhibited superior catalytic activity for removing gaseous formaldehyde (HCHO) at ambient temperature, in comparison with bulk counterpart with Bi2WO6 sheet thickness of tens of nanometers. The ultrathin structure endowed the Pt-BWO-NS sample with larger specific surface area, which can provide abundant surface active sites for HCHO adsorption and facilitate the homogeneous dispersion of Pt NPs. X-ray photoelectron spectroscopy and hydrogen temperature-programmed reduction analyses revealed the interaction between the Bi2WO6 support and Pt species, which is crucial for activating surface oxygen atoms to participate in the catalytic HCHO oxidation process. By conducting in situ diffuse reflectance infrared Fourier transform spectroscopy under different atmospheres, i.e., gaseous HCHO in nitrogen or oxygen (O2), the reaction mechanism and the role of O2 were elucidated, with dioxymethylene, formate and linearly adsorbed carbon monoxide identified as the main reaction intermediates. This study may provide new enlightenment on fabricating novel 2D nanomaterials for efficient indoor air purification and potentially other environmental applications.

  19. Low-temperature synthesis and structural properties of ferroelectric K 3WO 3F 3 elpasolite

    Science.gov (United States)

    Atuchin, V. V.; Gavrilova, T. A.; Kesler, V. G.; Molokeev, M. S.; Aleksandrov, K. S.

    2010-06-01

    Low-temperature ferroelectric G2 polymorph of K 3WO 3F 3 has been prepared by chemical synthesis. Structural and chemical properties of the final product have been evaluated with X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Structure parameters of G2-K 3WO 3F 3 are refined by the Rietveld method from XRD data measured at room temperature (space group Cm, Z = 2, a = 8.7350(3) Å, b = 8.6808(5) Å, c = 6.1581(3) Å, β = 135.124(3) Å, V = 329.46(3) Å 3; RB = 2.47%). Partial ordering of oxygen and fluorine atoms has been found over anion positions. Mechanism of ferroelectric phase transition in A 2BMO 3F 3 oxyfluorides is discussed.

  20. Eliminating degradation and uncovering ion-trapping dynamics in electrochromic WO3 thin films

    Science.gov (United States)

    Wen, Rui-Tao; Granqvist, Claes G.; Niklasson, Gunnar A.

    2015-01-01

    Amorphous WO3 thin films are of keen interest as cathodic electrodes in transmittance-modulating electrochromic devices. However, these films suffer from ion-trapping-induced degradation of optical modulation and reversibility upon extended Li+-ion exchange. Here, we demonstrate that ion-trapping-induced degradation, which is commonly believed to be irreversible, can be successfully eliminated by constant-current-driven de-trapping, i.e., WO3 films can be rejuvenated and regain their initial highly reversible electrochromic performance. Pronounced ion-trapping occurs when x exceeds ~0.65 in LixWO3 during ion insertion. We find two main kinds of Li+-ion trapping sites (intermediate and deep) in WO3, where the intermediate ones are most prevalent. Li+-ions can be completely removed from intermediate traps but are irreversibly bound in deep traps. Our results provide a general framework for developing and designing superior electrochromic materials and devices. PMID:26259104

  1. Photocatalytic activity of titanium dioxide modified by Fe2O3 nanoparticles

    International Nuclear Information System (INIS)

    Wodka, Dawid; Socha, Robert P.; Bielańska, Elżbieta; Elżbieciak-Wodka, Magdalena; Nowak, Paweł; Warszyński, Piotr

    2014-01-01

    Highlights: • 1% Fe 2 O 3 /TiO 2 composite showing high activity in the photocatalytic oxidation of organics was synthetized. • Electrochemical analysis indicated that surface modification of Degussa P25 by Fe 2 O 3 causes the appearance of surface states in such a material. • The enhanced activity of the prepared composite may be ascribed to the occurrence of the photo-Fenton process. - Abstract: Photocatalytic activity of Fe 2 O 3 /TiO 2 composites obtained by precipitation was investigated. The composite material containing 1.0 wt% of iron(III) oxide nanoparticles was obtained by depositing Fe 2 O 3 on the Evonic-Degussa P25 titania surface. SEM, XPS, DRS, CV and EIS techniques were applied to examine synthetized pale orange photocatalyst. The XPS measurements revealed that iron is present mainly in the +3 oxidation state but iron in the +2 oxidation state can be also detected. Electrochemical analysis indicated that surface modification of Degussa P25 by Fe 2 O 3 causes the appearance of surface states in such a material. Nevertheless, based on the DRS measurement it was shown that iron(III) oxide nanoparticles modified the P25 spectral properties but they did not change the band gap width. The photocatalytic activity of Fe 2 O 3 /TiO 2 composite was compared to photocatalytic activity of pristine P25 in photooxidation reaction of model compounds: oxalic acid (OxA) and formic acid (FA). Photodecomposition reaction was investigated in a batch reactor containing aqueous suspension of a photocatalyst illuminated by either UV or artificial sunlight (halogen lamp). The tests proved that nanoparticles deposited on titania surface triggers the increase in photocatalytic activity, this increase depends however on the decomposed substance

  2. Proximity hybridization-regulated catalytic DNA hairpin assembly for electrochemical immunoassay based on in situ DNA template-synthesized Pd nanoparticles

    International Nuclear Information System (INIS)

    Zhou, Fuyi; Yao, Yao; Luo, Jianjun; Zhang, Xing; Zhang, Yu; Yin, Dengyang; Gao, Fenglei; Wang, Po

    2017-01-01

    Novel hybridization proximity-regulated catalytic DNA hairpin assembly strategy has been proposed for electrochemical immunoassay based on in situ DNA template-synthesized Pd nanoparticles as signal label. The DNA template-synthesized Pd nanoparticles were characterized with atomic force microscopic and X-ray photoelectron spectroscopy. The highly efficient electrocatalysis by DNA template synthesized Pd nanoparticles for NaBH 4 oxidation produced an intense detection signal. The label-free electrochemical method achieved the detection of carcinoembryonic antigen (CEA) with a linear range from 10 −15 to 10 −11  g mL −1 and a detection limit of 0.43 × 10 −15  g mL −1 . Through introducing a supersandwich reaction to increase the DNA length, the electrochemical signal was further amplified, leading to a detection limit of 0.52 × 10 −16  g mL −1 . And it rendered satisfactory analytical performance for the determination of CEA in serum samples. Furthermore, it exhibited good reproducibility and stability; meanwhile, it also showed excellent specificity due to the specific recognition of antigen by antibody. Therefore, the DNA template synthesized Pd nanoparticles based signal amplification approach has great potential in clinical applications and is also suitable for quantification of biomarkers at ultralow level. - Graphical abstract: A novel label-free and enzyme-free electrochemical immunoassay based on proximity hybridization-regulated catalytic DNA hairpin assemblies for recycling of the CEA. - Highlights: • A novel enzyme-free electrochemical immunosensor was developed for detection of CEA. • The signal amplification was based on catalytic DNA hairpin assembly and DNA-template-synthesized Pd nanoparticles. • The biosensor could detect CEA down to 0.52 × 10 −16  g mL −1 level with a dynamic range spanning 5 orders of magnitude.

  3. Environmentally responsive surface-modified silica nanoparticles for enhanced oil recovery

    International Nuclear Information System (INIS)

    Behzadi, Abed; Mohammadi, Aliasghar

    2016-01-01

    Environmentally responsive surface-modified nanoparticles are colloidal nanoparticles coated with, at least, two physicochemically distinct surface groups. Recent advances in the synthesis and production of nanoparticles have enabled the production of environmentally responsive surface-modified nanoparticles with both hydrophilic and hydrophobic surface groups. These nanoparticles act like colloidal surfactants. In this paper, environmentally responsive surface-modified silica nanoparticles are synthesized and used for enhancement of oil recovery. For this purpose, silica nanoparticles are coated with polyethylene glycol chains as hydrophilic agent and propyl chains as hydrophobic agent at various quantities, and their ability to modulate oil–water interface properties and oil recovery is examined. Oil–water interfacial tension and water surface tension are decreased by 50 % in the presence of silica nanoparticles coated with both agents. Measuring oil-drop contact angle on oil-wetted glass slides and carbonate rock sections, after aging in various surface-modified silica nanofluids, indicates that the wettability of various oil-wetted surfaces is modified from strongly oil-wet to water-wet. Flooding nanofluids to glass micro-models and pore-level investigations demonstrate that surface modification of silica nanoparticles, specially, with both hydrophilic and hydrophobic agents improves considerably their performance in increasing oil recovery and wettability alteration.

  4. Environmentally responsive surface-modified silica nanoparticles for enhanced oil recovery

    Energy Technology Data Exchange (ETDEWEB)

    Behzadi, Abed; Mohammadi, Aliasghar, E-mail: amohammadi@sharif.edu [Sharif University of Technology, Department of Chemical and Petroleum Engineering (Iran, Islamic Republic of)

    2016-09-15

    Environmentally responsive surface-modified nanoparticles are colloidal nanoparticles coated with, at least, two physicochemically distinct surface groups. Recent advances in the synthesis and production of nanoparticles have enabled the production of environmentally responsive surface-modified nanoparticles with both hydrophilic and hydrophobic surface groups. These nanoparticles act like colloidal surfactants. In this paper, environmentally responsive surface-modified silica nanoparticles are synthesized and used for enhancement of oil recovery. For this purpose, silica nanoparticles are coated with polyethylene glycol chains as hydrophilic agent and propyl chains as hydrophobic agent at various quantities, and their ability to modulate oil–water interface properties and oil recovery is examined. Oil–water interfacial tension and water surface tension are decreased by 50 % in the presence of silica nanoparticles coated with both agents. Measuring oil-drop contact angle on oil-wetted glass slides and carbonate rock sections, after aging in various surface-modified silica nanofluids, indicates that the wettability of various oil-wetted surfaces is modified from strongly oil-wet to water-wet. Flooding nanofluids to glass micro-models and pore-level investigations demonstrate that surface modification of silica nanoparticles, specially, with both hydrophilic and hydrophobic agents improves considerably their performance in increasing oil recovery and wettability alteration.

  5. Comparative studies of monoclinic and orthorhombic WO3 films used for hydrogen sensor fabrication on SiC crystal

    International Nuclear Information System (INIS)

    Zuev, V V; Romanov, R I; Fominski, V Y; Grigoriev, S N; Volosova, M A; Demin, M V

    2016-01-01

    Amorphous WO x films were prepared on the SiC crystal by using two different methods, namely, reactive pulsed laser deposition (RPLD) and reactive deposition by ion sputtering (RDIS). After deposition, the WO x films were annealed in an air. The RISD film possessed a m-WO 3 structure and consisted of closely packed microcrystals. Localized swelling of the films and micro-hills growth did not destroy dense crystal packing. RPLD film had layered β-WO 3 structure with relatively smooth surface. Smoothness of the films were destroyed by localized swelling and the micro-openings formation was observed. Comparative study of m-WO 3 /SiC, Pt/m-WO 3 /SiC, and P-WO 3 /SiC samples shows that structural characteristics of the WO 3 films strongly influence on the voltage/current response as well as on the rate of current growth during H 2 detection at elevated temperatures. (paper)

  6. Optical and electrochromic properties of Sn:WO3 cermets

    International Nuclear Information System (INIS)

    Ashrit, P.V.; Bader, G.; Girouard, F.E.; Truong, V.V.

    1989-01-01

    This paper discusses optical and electrochromic properties of Sn:WO 3 cermets deposited by alternate layer thermal deposition. These cermets exhibit electrical and optical behavior in the as deposited state. The inclusion of Sn in the WO 3 matrix enhances the Electrical conductivity of the system and renders them fairly transparent in the visible region. The electrochromic behavior of such systems is studied under both proton and Li + ion injection. The good conductivity and good transmission combined with good electrochromic characteristics of these systems indicate the possibility of utilizing this type of cermet for the dual role of transparent conductor (TC) and electrochromic (EC) layer

  7. Gelatin modified lipid nanoparticles for anti- viral drug delivery.

    Science.gov (United States)

    K S, Joshy; S, Snigdha; Kalarikkal, Nandakumar; Pothen, Laly A; Thomas, Sabu

    2017-10-01

    The major challenges to clinical application of zidovudine are its moderate aqueous solubility and relative short half-life and serious side effects due to frequent administrations. We investigated the preparation of zidovudine-loaded nanoparticles based on lipids which were further modified with the polymer gelatin. Formulation and stability of the modified nanoparticles were analysed from the physico-chemical characterizations. The interactions of nanoparticles with blood components were tested by haemolysis and aggregation studies. The drug content and entrapment efficiencies were assessed by UV analysis. The effect of nanoparticles on protein adsorption was assessed by native polyacrylamide gel electrophoresis (PAGE). In vitro release studies showed a sustained release profile of zidovudine. In vitro cytotoxicity and cellular uptake of the zidovudine-loaded nanoparticles were performed in MCF-7 and neuro 2a brain cells. The enhanced cellular internalization of drug loaded modified nanoparticles in both the cell lines were revealed by fluorescence microscopy. Hence the present study focuses on the feasibility of zidovudine-loaded polymer modified lipid nanoparticles as carriers for safe and efficient HIV/AIDS therapy. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Characterization of Porous WO3 Electrochromic Device by Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Chien Chon Chen

    2013-01-01

    Full Text Available This paper concerns the microstructure of the anodic tungsten oxide (WO3 and its use in an electrochromic (EC glass device. When voltages between 100 V and 160 V were applied to tungsten film for 1 h under 0.4 wt. % NaF electrolyte, porous WO3 film was formed. The film, which had a large surface area, was used as electrochromic film for EC glass. The average transmittance in a visible region of the spectrum for a 144 cm2 EC device was above 75% in the bleached state and below 40% in the colored state, respectively. Repeatability using of the colored/bleached cycles was tested good by a cyclic voltammograms method. The internal impedance values under colored and bleached states were detected and simulated using an electrical impedance spectra (EIS technique. The EC glass impedance characteristics were simulated using resistors, capacitors, and Warburg impedance. The ITO/WO3, WO3/electrolyte, electrolyte/NiO, and NiO/ITO interfaces can be simulated using a resistance capacitance (RC parallel circuits, and bulk materials such as the indium tin oxide (ITO and conducting wire can be simulated by using a series of resisters.

  9. Influence of Liquid Petroleum Gas on the Electrical Parameters of the WO3 Thick Film

    Directory of Open Access Journals (Sweden)

    R. S. KHADAYATE

    2007-02-01

    Full Text Available In this work, the WO3 thick films were prepared by standard screen-printing technology. These films were characterized by x-ray diffraction (XRD measurements and scanning electron microscopy (SEM. Influence of LPG on the electrical properties of the prepared WO3 thick film is reported. It was observed that the slope of the Arrhenius curves of the WO3 thick film decreased as the medium changed from pure air to 100 ppm LPG in air. From I-V characteristics, it was observed that the WO3 thick film exhibit highest sensitivity to 50 ppm LPG in air at 400oC.

  10. Evaluate humidity sensing properties of novel TiO2–WO3 composite material

    International Nuclear Information System (INIS)

    Lin, Wang-De; Lai, De-Sheng; Chen, Min-Hung; Wu, Ren-Jang; Chen, Fu-Chou

    2013-01-01

    Graphical abstract: TiO 2 –WO 3 (1:1) showed better humidity sensing properties than others within the range of 12–90% relative humidity (RH), the response and recovery time were about 20 s and 160 s, respectively. Compared to the previous studies, the prepared sensor exhibits higher sensitivity (S = 451) and the low hysteresis value was around 0.13% at 32% RH. - Highlights: • Novel TiO 2 –WO 3 composite material was prepared for humidity sensor. • The sensor exhibits higher sensitivity (S = 451). • Low hysteresis value was around 0.13% at 32% RH. - Abstract: A novel TiO 2 –WO 3 composite material was prepared using a different proportion of TiO 2 and WO 3 to that investigated in previous studies. The obtained mesoporous material was characterized using X-ray diffraction, Fourier transform infrared spectrometry, transmission electron microscopy, energy dispersive X-ray spectroscopy, and N 2 adsorption-desorption techniques. The humidity-sensing properties were measured using an inductance, capacitance and resistance analyzer. The results demonstrated that the TiO 2 –WO 3 sample with a ratio of 1:1 showed better humidity sensing properties. Compared to previous studies, the prepared sensor exhibited higher sensitivity (S = 451) and the lower hysteresis value was around 0.13% at 32% RH. Complex impedance analysis indicated that the enhanced humidity sensitivity was probably due to spherical Brunauer–Emmett–Teller surface area and the hetero-junction between TiO 2 –WO 3 thin films, while the impedance varied about three orders of magnitude. Our results demonstrated the potential application of TiO 2 –WO 3 composite for fabricating high performance humidity sensors

  11. Esterification of industrial-grade palm fatty acid distillate over modified ZrO{sub 2} (with WO{sub 3}-, SO{sub 4} -and TiO{sub 2}-): Effects of co-solvent adding and water removal

    Energy Technology Data Exchange (ETDEWEB)

    Mongkolbovornkij, P.; Laosiripojana, N. [The Joint Graduate School of Energy and Environment, King Mongkut' s University of Technology Thonburi (Thailand); Champreda, V. [National Center for Genetic Enginnering and Biotechnology (BIOTEC), Pathumthani (Thailand); Sutthisripok, W. [Department of Mining and Materials Engineering, Prince of Songkla University, Songkhla (Thailand)

    2010-11-15

    The esterification of palm fatty acid distillate (PFAD), a by-product from palm oil industry, in the presence of three modified zirconia-based catalysts i.e. SO{sub 4}-ZrO{sub 2}, WO{sub 3}-ZrO{sub 2} and TiO{sub 2}-ZrO{sub 2} (with several sulfur- and tungsten-loading contents, Ti/Zr molar ratios, and calcination temperatures) was studied. It was found that, among all synthesized catalysts, the reaction in the presence of SO{sub 4}-ZrO{sub 2} and WO{sub 3}-ZrO{sub 2} (with 1.8%SO{sub 4} calcined at 500 C and/or 20%WO{sub 3} calcined at 800 C) enhances relatively high fatty acid methyl ester (FAME) yield (84.9-93.7%), which was proven to relate with the high acid site density and specific surface area as well as the formation of tetragonal phase over these catalysts. The greater benefit of WO{sub 3}-ZrO{sub 2} over SO{sub 4}-ZrO{sub 2} was its high stability after several reaction cycles, whereas significant deactivation was detected over SO{sub 4}-ZrO{sub 2} due to the leaching of sulfur from catalyst. For further improvement, the addition of toluene as co-solvent was found to increase the FAME yield along with reduce the requirement of methanol to PFAD molar ratio (while maintains the FAME yield above 90%). Furthermore, it was observed that the presence of water in the feed considerably lower the FAME yield due to the catalyst surface interfering by water and the further hydrolysis of FAME back to fatty acids. We proposed here that the negative effect can be considerably minimized by adding molecular sieve to remove water from the feed and/or during the reaction. (author)

  12. A Facile Synthesis of Graphene-WO3 Nanowire Clusters with High Photocatalytic Activity for O2 Evolution

    Directory of Open Access Journals (Sweden)

    M.-J. Zhou

    2014-01-01

    Full Text Available In the present work, graphene-WO3 nanowire clusters were synthesized via a facile hydrothermal method. The obtained graphene-WO3 nanowire clusters were characterized by X-ray diffraction (XRD, transmission electron microscopy (TEM, X-ray photoelectron spectroscopy (XPS, Fourier transform infrared spectroscopy (FT-IR, Raman spectroscopy, and ultraviolet-visible diffuse reflectance spectroscopy (DRS techniques. The photocatalytic oxygen (O2 evolution properties of the as-synthesized samples were investigated by measuring the amount of evolved O2 from water splitting. The graphene-WO3 nanowire clusters exhibited enhanced performance compared to pure WO3 nanowire clusters for O2 evolution. The amount of evolved O2 from water splitting after 8 h for the graphene-WO3 nanowire clusters is ca. 0.345 mmol/L, which is more than 1.9 times as much as that of the pure WO3 nanowire clusters (ca. 0.175 mmol/L. The high photocatalytic activity of the graphene-WO3 nanowire clusters was attributed to a high charge transfer rate in the presence of graphene.

  13. Investigation of the optical property and structure of WO3 thin films with different sputtering depositions

    Science.gov (United States)

    Chen, Hsi-Chao; Jan, Der-Jun; Chen, Chien-Han; Huang, Kuo-Ting; Lo, Yen-Ming; Chen, Sheng-Hui

    2011-09-01

    The purpose of this research was to compare the optical properties and structure of tungsten oxide (WO3) thin films that was deposited by different sputtering depositions. WO3 thin films deposited by two different depositions of direct current (DC) magnetron sputtering and pulsed DC sputtering. A 99.95% WO3 target was used as the starting material for these depositions. These WO3 thin films were deposited on the ITO glass, PET and silicon substrate by different ratios of oxygen and argon. A shadow moiré interferometer would be introduced to measure the residual stress for PET substrate. RF magnetron sputtering had the large residual stress than the other's depositions. A Raman spectrum could exhibit the phase of oxidation of WO3 thin film by different depositions. At the ratio of oxygen and argon was about 1:1, and the WO3 thin films had the best oxidation. However, it was important at the change of the transmittance (ΔT = Tbleached - Tcolored) between the coloring and bleaching for the smart window. Therefore, we also found the WO3 thin films had the large variation of transmittance between the coloring and bleaching at the gas ratios of oxygen and argon of 1:1.

  14. MnWO{sub 4} nanocapsules: Synthesis, characterization and its electrochemical sensing property

    Energy Technology Data Exchange (ETDEWEB)

    Muthamizh, Selvamani; Suresh, Ranganathan; Giribabu, Krishnamoorthy; Manigandan, Ramadoss; Praveen Kumar, Sivakumar; Munusamy, Settu; Narayanan, Vengidusamy, E-mail: vnnara@yahoo.co.in

    2015-01-15

    Highlights: • Synthesis of MnWO{sub 4} nanocapsules without use of any other external reagent. • High crystalline MnWO{sub 4} was obtained with phase purity. • Electrochemical sensing platform based on MnWO{sub 4} for sensing quercetin. • Micromolar detection ability of MnWO{sub 4} modified GCE. - Abstract: Manganese tungstate (MnWO{sub 4}) was synthesized by surfactant free precipitation method. MnWO{sub 4} was characterized by using various spectroscopic techniques. The phase, crystalline nature and the morphological analysis were carried out using XRD, scanning electron microscopy (SEM), and high resolution transmission electron microscopy (HR-TEM). Further, FT-IR, Raman, and DRS-UV–Vis spectral analysis were carried out in order to ascertain the optical property and the presence of functional groups. From the analysis, the morphology of the MnWO{sub 4} was observed to be in capsules with breadth and thickness were in nm range. The oxidation state of tungsten (W), and manganese (Mn) were investigated using X-ray photo electron spectroscopy (XPS) and electron paramagnetic resonance spectroscopy (EPR). The synthesized MnWO{sub 4} nanocapsules were used to modify glassy carbon electrode (GCE) to detect quercetin.

  15. Luminescence properties of Nd3+-doped Y2O3 nanoparticles in organic media

    International Nuclear Information System (INIS)

    Cui, Xiaoxia; Hou, Chaoqi; Lu, Jiabao; Gao, Chao; Wei, Wei; Peng, Bo

    2011-01-01

    Nd 3+ -doped yttrium oxide nanoparticles (Y 2 O 3 :Nd) with cubic phase were obtained successfully by a glycine-nitrate solution combustion method. The results of Fourier transform infrared spectra (FTIR) showed that the -OH groups residing on the nanoparticles surfaces were reduced effectively by modifying with capping agent. The modified Y 2 O 3 :Nd nanoparticles displayed good monodispersity and excellent luminescence in N,N-dimethylformamide (DMF) solvent. Some optical parameters were calculated by Judd-Ofelt analysis based on absorption and fluorescence spectra. A relative large stimulated emission cross section, 1.7 x 10 -20 cm 2 , of the 4 F 3/2 → 4 I 11/2 transition was calculated. Theses results show that the modified Y 2 O 3 :Nd nanoparticles display good luminescence behavior in organic media. (orig.)

  16. WO3 and W Thermal Atomic Layer Etching Using "Conversion-Fluorination" and "Oxidation-Conversion-Fluorination" Mechanisms.

    Science.gov (United States)

    Johnson, Nicholas R; George, Steven M

    2017-10-04

    The thermal atomic layer etching (ALE) of WO 3 and W was demonstrated with new "conversion-fluorination" and "oxidation-conversion-fluorination" etching mechanisms. Both of these mechanisms are based on sequential, self-limiting reactions. WO 3 ALE was achieved by a "conversion-fluorination" mechanism using an AB exposure sequence with boron trichloride (BCl 3 ) and hydrogen fluoride (HF). BCl 3 converts the WO 3 surface to a B 2 O 3 layer while forming volatile WO x Cl y products. Subsequently, HF spontaneously etches the B 2 O 3 layer producing volatile BF 3 and H 2 O products. In situ spectroscopic ellipsometry (SE) studies determined that the BCl 3 and HF reactions were self-limiting versus exposure. The WO 3 ALE etch rates increased with temperature from 0.55 Å/cycle at 128 °C to 4.19 Å/cycle at 207 °C. W served as an etch stop because BCl 3 and HF could not etch the underlying W film. W ALE was performed using a three-step "oxidation-conversion-fluorination" mechanism. In this ABC exposure sequence, the W surface is first oxidized to a WO 3 layer using O 2 /O 3 . Subsequently, the WO 3 layer is etched with BCl 3 and HF. SE could simultaneously monitor the W and WO 3 thicknesses and conversion of W to WO 3 . SE measurements showed that the W film thickness decreased linearly with number of ABC reaction cycles. W ALE was shown to be self-limiting with respect to each reaction in the ABC process. The etch rate for W ALE was ∼2.5 Å/cycle at 207 °C. An oxide thickness of ∼20 Å remained after W ALE, but could be removed by sequential BCl 3 and HF exposures without affecting the W layer. These new etching mechanisms will enable the thermal ALE of a variety of additional metal materials including those that have volatile metal fluorides.

  17. Ultrasensitive ppb-level NO2 gas sensor based on WO3 hollow nanosphers doped with Fe

    Science.gov (United States)

    Zhang, Ziyue; haq, Mahmood; Wen, Zhen; Ye, Zhizhen; Zhu, Liping

    2018-03-01

    WO3 mesoporous hollow nanospheres doped with Fe synthesized by a facile method have mesoporous hollow nanospherical like morphology, small grain size (10 nm), high crystalline quality and ultrahigh surface area (165 m2/g). XRD spectra and Raman spectra indicate the Fe doping leading to the smaller cell parameters as compared to pure WO3, and the slight distortion in the crystal lattice produces a number of defects, making it a better candidate for gas sensing. XPS analysis shows that Fe-doped WO3 mesoporous hollow nanospheres have more oxygen vacancies than pure WO3, which is beneficial to the adsorption of oxygen and NO2 and its surface reaction. The gas sensor based on Fe-WO3 exhibited excellent low ppb-level (10 ppb) NO2 detecting performance and outstanding selectivity.

  18. Synthesis, characterization and photocatalytic activity of porous WO{sub 3}/TiO{sub 2} hollow microspheres

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Liuyang [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); Si, Zhichun, E-mail: emsztsinghua@126.com [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); Weng, Duan [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); State Key Laboratory of New Ceramics and Fine Process, School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Yao, Youwei [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China)

    2014-09-15

    Porous WO{sub 3}/TiO{sub 2} hollow microspheres were prepared by a spray drying method for photodegradation of methylene blue and phenol. The catalysts were characterized by X-ray diffraction, Field Emission Scanning Electron Microscope, High Resolution Transmission Electron Microscope, N{sub 2} adsorption–desorption measurements, Raman spectrometer, UV–Vis Diffuse Reflectance Spectroscopy and Zeta-Meter measurements. The results showed that the tungsten oxides mainly existed in highly dispersed amorphous form on anatase when the loading amount of tungsten oxide was below 3 mol%. The improved photocatalytic activity under UV light irradiation of the WO{sub 3}/TiO{sub 2} catalyst mainly arises from the enhanced charge separation efficiency rather than the improved light absorbance by highly dispersed amorphous tungsten oxides. Highly dispersed amorphous WO{sub x} can form a shallowly trapped site due to its similar band structure with TiO{sub 2}. The strongly electron-withdrawing of tungsten oxide in highly dispersed state facilitates the electron transition between titanium and WO{sub x}, and consequently improves the charge separation. The enhanced acidity of catalyst by WO{sub x} in reactant environment also improved the charge separation efficiency due to the timely transition of holes and electrons accumulated on TiO{sub 2} and WO{sub x}, respectively. However, the improved photocatalytic activity under visible light irradiation of the WO{sub 3}/TiO{sub 2} catalyst mainly arises from light harvest. TiO{sub 2} containing 3 mol% WO{sub 3} displayed the highest photocatalytic activity under UV light irradiation while that containing 4 mol% WO{sub 3} present highest activity under visible light irradiation.

  19. Photovoltaic characterization of hybrid solar cells using surface modified TiO2 nanoparticles and poly(3-hexyl)thiophene

    International Nuclear Information System (INIS)

    Guenes, Serap; Marjanovic, Nenad; Nedeljkovic, Jovan M; Sariciftci, Niyazi Serdar

    2008-01-01

    We report on the photovoltaic performance of bulk heterojunction solar cells using novel nanoparticles of 6-palmitate ascorbic acid surface modified TiO 2 as an electron acceptor embedded into the donor poly(3-hexyl)thiophene (P3HT) matrix. Devices were fabricated by using P3HT with varying amounts of red TiO 2 nanoparticles (1:1, 1:2, 1:3 w-w ratio). The devices were characterized by measuring current-voltage characteristics under simulated AM 1.5 conditions. Incident photon to current efficiency (IPCE) was spectrally resolved. The nanoscale morphology of such organic/inorganic hybrid blends was also investigated using atomic force microscopy (AFM).

  20. Electrochemical catalytic activity of tungsten trioxide- modified graphite felt toward VO2+/VO2+ redox reaction

    International Nuclear Information System (INIS)

    Shen, Yang; Xu, Hongfeng; Xu, Pengcheng; Wu, Xiaoxin; Dong, Yiming; Lu, Lu

    2014-01-01

    A novel graphite felt electrode modified with tungsten trioxide (WO 3 ) was developed to improve the electrochemical performance of graphite felt toward the VO 2 + /VO 2+ redox pair. WO 3 was prepared using a hydrothermal method, and the morphology of WO 3 structures was investigated by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The electrochemical property of WO 3 -modified graphite felt toward VO 2 + /VO 2+ was carefully characterized using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements. The hydrogen-vanadium redox flow battery (H-VRFB) test indicates that single cells using 1.1 mg cm −2 WO 3 -modified graphite felt exhibited excellent performance at 70 mA cm −2 , and the corresponding coulombic, voltage, and energy efficiencies were 99.1%, 88.66% and 87.86%, respectively

  1. Ultrathin percolated WO{sub 3} cluster film and its resistive response to H{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Meng [Research Center for Solid State Physics and Materials, School of Mathematics and Physics, Suzhou University of Science and Technology, Suzhou 215009 (China); Department of Applied Physics and Materials Research Center, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (China); Wong, Man Hon; Huang, Jian Xing [Department of Applied Physics and Materials Research Center, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (China); Ong, Chung Wo, E-mail: c.w.ong@polyu.edu.hk [Department of Applied Physics and Materials Research Center, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (China)

    2014-11-05

    Highlights: • Ultrathin percolated network of WO{sub 3} clusters was fabricated. • The WO{sub 3} clusters are modeled by spherical caps connected by ultrafine linkages. • The ultrathin percolated network of WO{sub 3} clusters shows fast response rate to H{sub 2}. • The fast response is attributed to the rapid electrical switching of the linkages. • Improved H{sub 2} sensing properties may be achieved if narrower linkages are used. - Abstract: Thin films composed of tungsten oxide (WO{sub 3}) nanoclusters were fabricated by oxidizing supersonic cluster beam deposited tungsten films at various temperatures. Oxidation at 700 °C resulted in aggregation of the deposits, forming a percolated network of WO{sub 3} spherical caps connected by fine links. The resistance response of the palladium-(Pd-) coated film sample to hydrogen (H{sub 2}) was investigated. The response rate was faster than those of other samples oxidized at lower temperatures. This is the result of the rapid electrical switching of the intercluster links between the highly resistive depleted state and conducting hydrogenated state. The possibility of improving the H{sub 2} sensing response rate with the use of the percolated WO{sub 3} film structure is illustrated.

  2. Hydrothermal synthesis of hierarchical WO3 nanostructures for dye-sensitized solar cells

    International Nuclear Information System (INIS)

    Rashad, M.M.; Shalan, A.E.

    2014-01-01

    Hierarchical architectures consisting of one-dimensional (1D) nanostructures are of great interest for potential use in energy and environmental applications in recent years. In this work, hierarchical tungsten oxide (WO 3 ) has been synthesized via a facile hydrothermal route from ammonium metatungstate hydrate and implemented as photoelectrode for dye-sensitized solar cells. The urchin-like WO 3 micro-patterns are constructed by self-organized nanoscale length 1D building blocks, which are single crystalline in nature, grown along (001) direction and confirm an orthorhombic crystal phase. The obtained powders were investigated by XRD, SEM, TEM and UV-Vis Spectroscopy. The photovoltaic performance of dye-sensitized solar cells based on WO 3 photoanodes was investigated. With increasing the calcination temperature of the prepared nanopowders, the light-electricity conversion efficiency (η) was increased. The results were attributed to increase the crystallinity of the particles and ease of electron movement. The DSSC based on hierarchical WO 3 showed a short-circuit current, an open-circuit voltage, a fill factor, and a conversion efficiency of 4.241 mA/cm 2 , 0.656 V, 66.74, and 1.85 %, respectively. (orig.)

  3. Structural phototransformation of WO{sub 3} thin films detected by photoacoustic analysis

    Energy Technology Data Exchange (ETDEWEB)

    Pacheco, Argelia Perez, E-mail: ekargy@hotmail.com [Universidad Nacional Autonoma de Mexico, Laboratorio de Fotofisica y Peliculas Delgadas-CCADET, Ciudad Universitaria, Coyoacan, A.P. 70-186, C.P. 04510, Mexico, D.F. (Mexico); Montes de Oca, C. Oliva; Castaneda-Guzman, R.; Garcia, A. Esparza [Universidad Nacional Autonoma de Mexico, Laboratorio de Fotofisica y Peliculas Delgadas-CCADET, Ciudad Universitaria, Coyoacan, A.P. 70-186, C.P. 04510, Mexico, D.F. (Mexico)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer The phototransformation of WO{sub 3} thin films were studied by photoacoustic technique. Black-Right-Pointing-Pointer The phase transition in WO{sub 3} thin films was induced by laser irradiation fluence. Black-Right-Pointing-Pointer The onset and end of the phototransformation in the thin films was identified. Black-Right-Pointing-Pointer The ablation threshold for each sample was identified. - Abstract: The photoacoustic technique (PA) was used to detect the phase transformation from amorphous to crystalline state of tungsten oxide (WO{sub 3}) thin films induced by UV pulsed laser radiation at low energy (<1.5 mJ). The evolution of photoacoustic signal was studied by a correlation analysis, comparing successive signals at fluences ranging from 0 to 20 mJ/cm{sup 2}. In this interval, it was possible to observe structural changes and the ablation threshold in films due to incident laser fluence effect. Thin films of WO{sub 3} were deposited by DC reactive magnetron sputtering over glass substrates at different deposition times. The results obtained by correlation analysis were compared with Raman spectroscopy data.

  4. A Nanoparticle-Lectin Immunoassay Improves Discrimination of Serum CA125 from Malignant and Benign Sources.

    Science.gov (United States)

    Gidwani, Kamlesh; Huhtinen, Kaisa; Kekki, Henna; van Vliet, Sandra; Hynninen, Johanna; Koivuviita, Niina; Perheentupa, Antti; Poutanen, Matti; Auranen, Annika; Grenman, Seija; Lamminmäki, Urpo; Carpen, Olli; van Kooyk, Yvette; Pettersson, Kim

    2016-10-01

    Measurement of serum cancer antigen 125 (CA125) is the standard approach for epithelial ovarian cancer (EOC) diagnostics and follow-up. However, the clinical specificity is not optimal because increased values are also detected in healthy controls and in benign diseases. CA125 is known to be differentially glycosylated in EOC, potentially offering a way to construct CA125 assays with improved cancer specificity. Our goal was to identify carbohydrate-reactive lectins for discriminating between CA125 originating from EOC and noncancerous sources. CA125 from the OVCAR-3 cancer cell line, placental homogenate, and ascites fluid from patients with cirrhosis were captured on anti-CA125 antibody immobilized on microtitration wells. A panel of lectins, each coated onto fluorescent europium-chelate-doped 97-nm nanoparticles (Eu(+3)-NPs), was tested for detection of the immobilized CA125. Serum samples from high-grade serous EOC or patients with endometriosis and healthy controls were analyzed. By using macrophage galactose-type lectin (MGL)-coated Eu(+3)-NPs, an analytically sensitive CA125 assay (CA125(MGL)) was achieved that specifically recognized the CA125 isoform produced by EOC, whereas the recognition of CA125 from nonmalignant conditions was reduced. Serum CA125(MGL) measurement better discriminated patients with EOC from endometriosis compared to conventional immunoassay. The discrimination was particularly improved for marginally increased CA125 values and for earlier detection of EOC progression. The new CA125(MGL) assay concept could help reduce the false-positive rates of conventional CA125 immunoassays. The improved analytical specificity of this test approach is dependent on a discriminating lectin immobilized in large numbers on Eu(+3)-NPs, providing both an avidity effect and signal amplification. © 2016 American Association for Clinical Chemistry.

  5. Study of phase equilibria and glass formation in the CaO-WO3-P2O5 system

    International Nuclear Information System (INIS)

    Bielis, I.Ya.

    1980-01-01

    The method of quenching has been used to investigate the liquidus surface of a portion of the CaO-WO 3 -P 2 O 5 system limited by the Ca(PO 3 ) 2 -W 2 O 3 (PO 4 ) 2 and CaWO 4 -Ca 2 P 2 O 7 cross-sections. The primary crystallization fields on the compounds: WO 3 , W 2 O 3 (PO 4 ) 2 , CaWO 4 , Ca 2 P 7 O 7 , Ca(PO 3 ) 2 are separated. The liquidus surface isotherms at 900, 1000, 1100 and 1200 deg C have been plotted on the concentration triangle plane. It has been found that the cross-sections of W 2 O 3 (PO 4 ) 2 -Ca(PO 3 ) 2 , WO 3 -Ca(PO 3 ) 2 , WO 3 -Ca 2 P 2 O 7 and CaWO 4 -Ca 2 P 2 O 7 are eutectic-type quasi-binary systems. The position of the glass transition region in the CaO-WO 3 -P 2 O 5 system has been determined for the treatment temperatures of 1100, 1200 and 1300 deg C and a correlation between the configuration of the glass transition region and the phase diagram of the system has been demonstrated [ru

  6. Degradation of organic dyes using spray deposited nanocrystalline stratified WO3/TiO2 photoelectrodes under sunlight illumination

    Science.gov (United States)

    Hunge, Y. M.; Yadav, A. A.; Mahadik, M. A.; Bulakhe, R. N.; Shim, J. J.; Mathe, V. L.; Bhosale, C. H.

    2018-02-01

    The need to utilize TiO2 based metal oxide hetero nanostructures for the degradation of environmental pollutants like Rhodamine B and reactive red 152 from the wastewater using stratified WO3/TiO2 catalyst under sunlight illumination. WO3, TiO2 and stratified WO3/TiO2 catalysts were prepared by a spray pyrolysis method. It was found that the stratified WO3/TiO2 heterostructure has high crystallinity, no mixed phase formation occurs, strong optical absorption in the visible region of the solar spectrum, and large surface area. The photocatalytic activity was tested for degradation of Rhodamine B (Rh B) and reactive red 152 in an aqueous medium. TiO2 layer in stratified WO3/TiO2 catalyst helps to extend its absorption spectrum in the solar light region. Rh B and Reactive red 152is eliminated up to 98 and 94% within the 30 and 40 min respectively at optimum experimental condition by stratified WO3/TiO2. Moreover, stratified WO3/TiO2 photoelectrode has good stability and reusability than individual TiO2 and WO3 thin film in the degradation of Rh B and reactive red 152. The photoelectrocatalytic experimental results indicate that stratified WO3/TiO2 photoelectrode is a promising material for dye removal.

  7. Humidity sensing properties of WO3 thick film resistor prepared by screen printing technique

    International Nuclear Information System (INIS)

    Garde, Arun S

    2014-01-01

    Highlights: • Polycrystalline WO 3 Thick films are fabricated by screen printing technique. • Monoclinic phases were the majority in formation of films. • The peak at 1643 cm −1 shows stretching vibrations attributed to W-OH of adsorbed H 2 O. • Absorption peaks in the range 879–650 cm −1 are attributed to the stretching W-O-W bonds. • Increase in resistance with decrease in RH when exposed to 20–100% RH. - Abstract: Thick films of tungsten oxide based were prepared using standard screen printing technique. To study the effect of temperature on the thick films were fired at different temperature for 30 min in air atmosphere. The WO 3 thick films were characterized with X-ray diffraction, scanning electron microscopy and EDAX for elemental analysis. The formation of mixed phases of the film together with majority of monoclinic phase was observed. IR spectra confirm the peak at 1643 cm −1 clearly shows stretching vibrations attributed to the W-OH bending vibration mode of the adsorbed water molecules. The absorption peaks in the range 879–650 cm −1 are attributed to the stretching W-O-W bonds (i.e. ν [W-O inter -W]). The peak located at 983 cm −1 belong to W=O terminal of cluster boundaries. A change in the resistance was observed with respect to the relative humidity when the WO 3 thick films were exposed to a wide humidity range of 20–100%. An increasing firing temperature of WO 3 film increases with the sensitivity. The parameters such as sensitivity and hysteresis of the WO 3 film sensors have been evaluated

  8. X-ray photoelectron spectroscopy study of BaWO{sub 4} and Ba{sub 2}CaWO{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Capece, Angela M., E-mail: acapece@pppl.gov [California Institute of Technology, Pasadena, CA (United States); Polk, James E. [Jet Propulsion Laboratory, Pasadena, CA (United States); Shepherd, Joseph E. [California Institute of Technology, Pasadena, CA (United States)

    2014-12-15

    Highlights: • XPS reference spectra for Ba{sub 2}CaWO{sub 6} and BaWO{sub 4} are presented. • Binding energies of Ba 3d and W 4f lines are 0.7 eV higher for BaWO{sub 4} than Ba{sub 2}CaWO{sub 6}. • Ca 2p spectrum contains two sets of Ca 2p doublets attributed to Ba{sub 2}CaWO{sub 6} and CaCO{sub 3}. - Abstract: XPS reference spectra for Ba{sub 2}CaWO{sub 6} and BaWO{sub 4} are presented, including high resolution spectra of the Ba 3d, W 4f, C 1s, Ca 2p, and O 1s lines. The peak locations and full widths at half maximum are also given. The binding energies of the Ba 3d and W 4f lines are 0.7 eV higher for BaWO{sub 4} than for Ba{sub 2}CaWO{sub 6}. The Ca 2p spectrum contains two sets of Ca 2p doublets that were attributed to Ba{sub 2}CaWO{sub 6} and CaCO{sub 3}.

  9. Ligand-Modified Human Serum Albumin Nanoparticles for Enhanced Gene Delivery.

    Science.gov (United States)

    Look, Jennifer; Wilhelm, Nadine; von Briesen, Hagen; Noske, Nadja; Günther, Christine; Langer, Klaus; Gorjup, Erwin

    2015-09-08

    The development of nonviral gene delivery systems is a great challenge to enable safe gene therapy. In this study, ligand-modified nanoparticles based on human serum albumin (HSA) were developed and optimized for an efficient gene therapy. Different glutaraldehyde cross-linking degrees were investigated to optimize the HSA nanoparticles for gene delivery. The peptide sequence arginine-glycine-aspartate (RGD) and the HIV-1 transactivator of transduction sequence (Tat) are well-known as promising targeting ligands. Plasmid DNA loaded HSA nanoparticles were covalently modified on their surface with these different ligands. The transfection potential of the obtained plasmid DNA loaded RGD- and Tat-modified nanoparticles was investigated in vitro, and optimal incubation conditions for these preparations were studied. It turned out that Tat-modified HSA nanoparticles with the lowest cross-linking degree of 20% showed the highest transfection potential. Taken together, ligand-functionalized HSA nanoparticles represent promising tools for efficient and safe gene therapy.

  10. Gd2O3 nanoparticles stabilized by hydrothermally modified dextrose for positive contrast magnetic resonance imaging

    Science.gov (United States)

    Babić-Stojić, Branka; Jokanović, Vukoman; Milivojević, Dušan; Požek, Miroslav; Jagličić, Zvonko; Makovec, Darko; Arsikin, Katarina; Paunović, Verica

    2016-04-01

    Gd2O3 nanoparticles of a few nm in size and their agglomerates dispersed in dextrose derived polymer template were synthesized by hydrothermal treatment. The produced nanosized material was investigated by TEM, FTIR spectroscopy, SQUID measurements and NMR relaxometry. Biological evaluation of this material was done by crystal violet and MTT assays to determine the cell viability. Longitudinal and transverse NMR relaxivities of water diluted Gd2O3 nanoparticle dispersions measured at the magnetic field of 1.5 T, estimated to be r1(Gd2O3)=9.6 s-1 mM-1 in the Gd concentration range 0.1-30 mM and r2(Gd2O3)=17.7 s-1 mM-1 in the lower concentration range 0.1-0.8 mM, are significantly higher than the corresponding relaxivities measured for the standard contrast agent r1(Gd-DTPA)=4.1 s-1 mM-1 and r2(Gd-DTPA)=5.1 s-1 mM-1. The ratio of the two relaxivities for Gd2O3 nanoparticles r2/r1=1.8 is suitable for T1-weighted imaging. Good MRI signal intensities of the water diluted Gd2O3 nanoparticle dispersions were recorded at lower Gd concentrations 0.2-0.8 mM. The Gd2O3 samples did not exert any significant cytotoxic effects at Gd concentrations of 0.2 mM and below. These properties of the produced Gd2O3 nanoparticles in hydrothermally modified dextrose make them promising for potential application in MRI for the design of a positive MRI contrast agent.

  11. Structural and photoelectrochemical investigation of boron-modified nanostructured tungsten trioxide films

    International Nuclear Information System (INIS)

    Barczuk, Piotr J.; Krolikowska, Agata; Lewera, Adam; Miecznikowski, Krzysztof; Solarska, Renata; Augustynski, Jan

    2013-01-01

    We report a modification of nanostructured WO 3 films by doping with boron. The films were obtained by a direct one-step sol–gel route involving tungstic acid/polyethelene glycol precursor. Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) showed that the incorporation of boron results in the retention of a substantial amount of water and/or hydroxyl groups in the WO 3 lattice and at the surface of nanoparticles occurring despite high temperature (550 °C) annealing of the films. Another consequence of boron doping is the largely increased roughness factor revealed by atomic force microscopy (AFM) imaging. Both kinds of films are highly porous and consist of partly sintered particles with sizes in the range of tens of nanometers. The photoelectrochemical (PEC) studies performed under simulated solar AM 1.5 illumination showed significantly enhanced water oxidation photocurrents for B-WO 3 photoanodes, by about 25% higher than those for the undoped WO 3 films of similar thickness. The low extent of recombination of photogenerated charges was confirmed by incident photon-to-current conversion efficiencies (IPCEs) reaching 70% in the region of visible wavelengths at 420 nm. The improved PEC properties were attributed to the increased surface hydroxylation of B-WO 3 nanoparticles favoring water photo-oxidation reaction and to the larger surface area of the film exposed to the electrolyte

  12. CRYSTALLIZATION KINETICS OF POLYMERIC NANOCOMPOSITES BASED ON POLYAMIDE 12 MODIFIED BY Cr2O3 NANOPARTICLES

    Directory of Open Access Journals (Sweden)

    E. S. Shapoval

    2014-09-01

    Full Text Available In situ polymerization method is used for obtaining polymeric composites based on polyamide12 matrix (PA 12, filled with Cr2O3 nanoparticles. The carried out researches result in synthesis method development for polymeric nanocomposites based on PA 12 matrix filled with nano-sized Cr2O3magnetic particles providing uniform embedding of the filler into polymeric matrix without formation of nanoparticles agglomerates. Mechanical tests on samples compression are carried out. It is shown that mechanical properties of polymeric composites (Young’s modulus, durability limit are decreased for 20-30 % as compared with not modified PA 12 synthesized by means of the chosen method. The influence of the filler on crystallization morphology and kinetics of polymeric nanocomposites is determined by electron microscopy and differential scanning calorimetry. The values of crystallization degree, crystallization rate constant for different supercooling intervals and parameters of Avrami equation are obtained. The initial nucleation is shown to be going on according to non-thermal mechanism, and nanoparticles are not the germs of crystallization. It is stated that nanoparticles are embedded into polymeric matrix and uniformly allocated in crystallites. Research results can find their application at creation of electric and magnetic fields, micro-sized mechanical devices, and at development of new materials for 3D printers.

  13. Giant Persistent Photoconductivity of the WO3 Nanowires in Vacuum Condition

    Directory of Open Access Journals (Sweden)

    Huang Kai

    2011-01-01

    Full Text Available Abstract A giant persistent photoconductivity (PPC phenomenon has been observed in vacuum condition based on a single WO3 nanowire and presents some interesting results in the experiments. With the decay time lasting for 1 × 104 s, no obvious current change can be found in vacuum, and a decreasing current can be only observed in air condition. When the WO3 nanowires were coated with 200 nm SiO2 layer, the photoresponse almost disappeared. And the high bias and high electric field effect could not reduce the current in vacuum condition. These results show that the photoconductivity of WO3 nanowires is mainly related to the oxygen adsorption and desorption, and the semiconductor photoconductivity properties are very weak. The giant PPC effect in vacuum condition was caused by the absence of oxygen molecular. And the thermal effect combining with oxygen re-adsorption can reduce the intensity of PPC.

  14. Tungsten-based nanomaterials (WO{sub 3} & Bi{sub 2}WO{sub 6}): Modifications related to charge carrier transfer mechanisms and photocatalytic applications

    Energy Technology Data Exchange (ETDEWEB)

    Girish Kumar, S., E-mail: girichem@yahoo.co.in; Koteswara Rao, K.S.R., E-mail: raoksrk@gmail.com

    2015-11-15

    Graphical abstract: - Highlights: • Photocatalytic applications of WO{sub 3} and Bi{sub 2}WO{sub 6} based nanomaterial are reviewed. • Modifications to improve their performance are highlighted. • Charge carrier generation–separation–recombination is discussed. • Challenges and future prospects in this area are addressed. - Abstract: Heterogeneous photocatalysis is an ideal green energy technology for the purification of wastewater. Although titania dominates as the reference photocatalyst, its wide band gap is a bottleneck for extended utility. Thus, search for non-TiO{sub 2} based nanomaterials has become an active area of research in recent years. In this regard, visible light absorbing polycrystalline WO{sub 3} (2.4–2.8 eV) and Bi{sub 2}WO{sub 6} (2.8 eV) with versatile structure-electronic properties has gained considerable interest to promote the photocatalytic reactions. These materials are also explored in selective functional group transformation in organic reactions, because of low reduction and oxidation potential of WO{sub 3} CB and Bi{sub 2}WO{sub 6} VB, respectively. In this focused review, various strategies such as foreign ion doping, noble metal deposition and heterostructuring with other semiconductors designed for efficient photocatalysis is discussed. These modifications not only extend the optical response to longer wavelengths, but also prolong the life-time of the charge carriers and strengthen the photocatalyst stability. The changes in the surface-bulk properties and the charge carrier transfer dynamics associated with each modification correlating to the high activity are emphasized. The presence of oxidizing agents, surface modification with Cu{sup 2+} ions and synthesis of exposed facets to promote the degradation rate is highlighted. In depth study on these nanomaterials is likely to sustain interest in wastewater remediation and envisaged to signify in various green energy applications.

  15. Magnetophoretic separation ICP-MS immunoassay using Cs-doped multicore magnetic nanoparticles for the determination of salmonella typhimurium.

    Science.gov (United States)

    Jeong, Arong; Lim, H B

    2018-02-01

    In this work, a magnetophoretic separation ICP-MS immunoassay using newly synthesized multicore magnetic nanoparticles (MMNPs) was developed for the determination of salmonella typhimurium (typhi). The uniqueness of this method was the use of MMNPs doped with Cs for both separation and detection, which enable us to achieve fast analysis, high sensitivity, and good reliability. For demonstration, heat-killed typhi in a phosphate buffer solution was determined by ICP-MS after the MMNP-typhi reaction product was separated from unreacted MMNPs in a micropipette tip filled with 25% polyethylene glycol through magnetophoretic separation. The calibration curve obtained by plotting 133 Cs intensity vs. the number of synthetic standard, showed a coefficient of determination (R 2 ) of 0.94 with a limit of detection (LOD) of 102 cells/mL without cell culturing. Excellent recoveries, between 98-100%, were obtained from four replicates and compared with a sandwich-type ICP-MS immunoassay for further confirmation. Copyright © 2017 Elsevier B.V. All rights reserved.

  16. Removal of reactive red-120 and 4-(2-pyridylazo) resorcinol from aqueous samples by Fe3O4 magnetic nanoparticles using ionic liquid as modifier

    International Nuclear Information System (INIS)

    Absalan, Ghodratollah; Asadi, Mozaffar; Kamran, Sedigheh; Sheikhian, Leila; Goltz, Douglas M.

    2011-01-01

    Highlights: → Ionic liquids modify the dye-adsorption characteristics of magnetic nanoparticles. → Modified nanoparticles improved the sensitivity of dye measurements. → Water-solubility is an important factor for choosing an ionic liquid as a modifier for nanoparticles. - Abstract: The nanoparticles of Fe 3 O 4 as well as the binary nanoparticles of ionic liquid and Fe 3 O 4 (IL-Fe 3 O 4 ) were synthesized for removal of reactive red 120 (RR-120) and 4-(2-pyridylazo) resorcinol (PAR) as model azo dyes from aqueous solutions. The mean size and the surface morphology of the nanoparticles were characterized by TEM, DLS, XRD, FTIR and TGA techniques. Adsorption of RR-120 and PAR was studied in a batch reactor at different experimental conditions such as nanoparticle dosage, dye concentration, pH of the solution, ionic strength, and contact time. Experimental results indicated that the IL-Fe 3 O 4 nanoparticles had removed more than 98% of both dyes under the optimum operational conditions of a dosage of 60 mg, a pH of 2.5, and a contact time of 2 min when initial dyes concentrations of 10-200 mg L -1 were used. The maximum adsorption capacity of IL-Fe 3 O 4 was 166.67 and 49.26 mg g -1 for RR-120 and PAR, respectively. The isotherm experiments revealed that the Langmuir model attained better fits to the equilibrium data than the Freundlich model. The Langmuir adsorption constants were 5.99 and 3.62 L mg -1 for adsorptions of RR-120 and PAR, respectively. Both adsorption processes were endothermic and dyes could be desorbed from IL-Fe 3 O 4 by using a mixed NaCl-acetone solution and adsorbent was reusable.

  17. Electronic and optical properties of nanocrystalline WO3 thin films studied by optical spectroscopy and density functional calculations

    International Nuclear Information System (INIS)

    Johansson, Malin B; Niklasson, Gunnar A; Österlund, Lars; Baldissera, Gustavo; Persson, Clas; Valyukh, Iryna; Arwin, Hans

    2013-01-01

    The optical and electronic properties of nanocrystalline WO 3 thin films prepared by reactive dc magnetron sputtering at different total pressures (P tot ) were studied by optical spectroscopy and density functional theory (DFT) calculations. Monoclinic films prepared at low P tot show absorption in the near infrared due to polarons, which is attributed to a strained film structure. Analysis of the optical data yields band-gap energies E g ≈ 3.1 eV, which increase with increasing P tot by 0.1 eV, and correlate with the structural modifications of the films. The electronic structures of triclinic δ-WO 3 , and monoclinic γ- and ε-WO 3 were calculated using the Green function with screened Coulomb interaction (GW approach), and the local density approximation. The δ-WO 3 and γ-WO 3 phases are found to have very similar electronic properties, with weak dispersion of the valence and conduction bands, consistent with a direct band-gap. Analysis of the joint density of states shows that the optical absorption around the band edge is composed of contributions from forbidden transitions (>3 eV) and allowed transitions (>3.8 eV). The calculations show that E g in ε-WO 3 is higher than in the δ-WO 3 and γ-WO 3 phases, which provides an explanation for the P tot dependence of the optical data. (paper)

  18. Electronic and optical properties of nanocrystalline WO3 thin films studied by optical spectroscopy and density functional calculations

    Science.gov (United States)

    Johansson, Malin B.; Baldissera, Gustavo; Valyukh, Iryna; Persson, Clas; Arwin, Hans; Niklasson, Gunnar A.; Österlund, Lars

    2013-05-01

    The optical and electronic properties of nanocrystalline WO3 thin films prepared by reactive dc magnetron sputtering at different total pressures (Ptot) were studied by optical spectroscopy and density functional theory (DFT) calculations. Monoclinic films prepared at low Ptot show absorption in the near infrared due to polarons, which is attributed to a strained film structure. Analysis of the optical data yields band-gap energies Eg ≈ 3.1 eV, which increase with increasing Ptot by 0.1 eV, and correlate with the structural modifications of the films. The electronic structures of triclinic δ-WO3, and monoclinic γ- and ε-WO3 were calculated using the Green function with screened Coulomb interaction (GW approach), and the local density approximation. The δ-WO3 and γ-WO3 phases are found to have very similar electronic properties, with weak dispersion of the valence and conduction bands, consistent with a direct band-gap. Analysis of the joint density of states shows that the optical absorption around the band edge is composed of contributions from forbidden transitions (>3 eV) and allowed transitions (>3.8 eV). The calculations show that Eg in ε-WO3 is higher than in the δ-WO3 and γ-WO3 phases, which provides an explanation for the Ptot dependence of the optical data.

  19. Electronic structure of nanoparticles of substoichometric hexagonal tungsten oxides

    International Nuclear Information System (INIS)

    Khyzhun, O Y; Solonin, Y M

    2007-01-01

    X-ray photoelectron spectroscopy (XPS), X-ray emission spectroscopy (XES) and X-ray absorption spectroscopy (XAS) methods were used to study the electronic structure of hexagonal h-WO 3 and h-WO 2.8 nanoparticles. For comparison, nanopowder substoichiometric monoclinic tungsten oxides with close content of oxygen atoms, namely m-WO 3 and m-WO 2.77 compounds, were also investigated. For the mentioned oxides, XPS valence-band and corelevel spectra, XES O Kα bands and XAS W L III and O 1s edges were derived. The XPS valence-band spectra and O Kα emission bands in the mentioned hexagonal and monoclinic tungsten oxides were compared on a common energy scale. Both the O Kα bands and XPS valence-band spectra broaden somewhat in the sequences h-WO 3 → h-WO 2.8 and m-WO 3 → m-WO 2.77 , with the half-widths of the spectra being somewhat higher for the hexagonal oxides as compared with those for the monoclinic compounds. The effective positive charge state of tungsten atoms in h-WO 2.8 is very close to that in m-WO 2.77 , but the negative charge states of oxygen atoms are close to each other for all the tungsten oxides under consideration

  20. In vitro placental model optimization for nanoparticle transport studies

    Directory of Open Access Journals (Sweden)

    Cartwright L

    2012-01-01

    Full Text Available Laura Cartwright1, Marie Sønnegaard Poulsen2, Hanne Mørck Nielsen3, Giulio Pojana4, Lisbeth E Knudsen2, Margaret Saunders1, Erik Rytting2,51Bristol Initiative for Research of Child Health (BIRCH, Biophysics Research Unit, St Michael's Hospital, UH Bristol NHS Foundation Trust, Bristol, UK; 2University of Copenhagen, Faculty of Health Sciences, Department of Public Health, 3University of Copenhagen, Faculty of Pharmaceutical Sciences, Department of Pharmaceutics and Analytical Chemistry, Copenhagen, Denmark; 4Department of Environmental Sciences, Informatics and Statistics, University Ca' Foscari Venice, Venice, Italy; 5Department of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, Texas, USABackground: Advances in biomedical nanotechnology raise hopes in patient populations but may also raise questions regarding biodistribution and biocompatibility, especially during pregnancy. Special consideration must be given to the placenta as a biological barrier because a pregnant woman's exposure to nanoparticles could have significant effects on the fetus developing in the womb. Therefore, the purpose of this study is to optimize an in vitro model for characterizing the transport of nanoparticles across human placental trophoblast cells.Methods: The growth of BeWo (clone b30 human placental choriocarcinoma cells for nanoparticle transport studies was characterized in terms of optimized Transwell® insert type and pore size, the investigation of barrier properties by transmission electron microscopy, tight junction staining, transepithelial electrical resistance, and fluorescein sodium transport. Following the determination of nontoxic concentrations of fluorescent polystyrene nanoparticles, the cellular uptake and transport of 50 nm and 100 nm diameter particles was measured using the in vitro BeWo cell model.Results: Particle size measurements, fluorescence readings, and confocal microscopy indicated both cellular uptake of

  1. Bi3+ sensitized Y2WO6:Ln3+ (Ln=Dy, Eu, and Sm) phosphors for solar spectral conversion.

    Science.gov (United States)

    Huang, M N; Ma, Y Y; Xiao, F; Zhang, Q Y

    2014-01-01

    The phosphors of Y2WO6:Bi3+, Ln3+ (Ln=Dy, Eu and Sm) were synthesized by solid-state reaction in this study. The crystal structure, photoluminescence properties and energy transfer mechanism were investigated. By introducing Bi3+ ions, the excitation band of the phosphors was broadened to be 250-380 nm, which could be absorbed by the dye-sensitized solar cells (DSSCs). The overlap between excitation of W-O groups/Bi3+ and the emission of Ln3+ (Dy, Eu, and Sm) indicated that the probability of energy transfer from W-O groups and Bi3+ to Ln3+. The energy transfer efficiency from Bi3+ to Ln3+ (Ln=Dy, Eu and Sm) are calculated to be 16%, 20% and 58%. This work suggested that Y2WO6:Bi3+, Ln3+ (Ln=Dy, Eu and Sm) might be a promising ultraviolet-absorbing luminescent converter to enhance the photoelectrical conversion efficiency of dye-sensitized solar cells (DSSCs). Copyright © 2013 Elsevier B.V. All rights reserved.

  2. Nanosilver-penetrated polyion graphene complex membrane for mediator-free amperometric immunoassay of alpha-fetoprotein using nanosilver-coated silica nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Tang Juan [Ministry of Education Key Laboratory of Analysis and Detection for Food Safety, Fujian Provincial Key Laboratory of Analysis and Detection Technology for Food Safety, Department of Chemistry, Fuzhou University, Fuzhou 350108 (China); Tang Dianping, E-mail: dianping.tang@fzu.edu.c [Ministry of Education Key Laboratory of Analysis and Detection for Food Safety, Fujian Provincial Key Laboratory of Analysis and Detection Technology for Food Safety, Department of Chemistry, Fuzhou University, Fuzhou 350108 (China); Su Biling; Li Qunfang; Qiu Bin [Ministry of Education Key Laboratory of Analysis and Detection for Food Safety, Fujian Provincial Key Laboratory of Analysis and Detection Technology for Food Safety, Department of Chemistry, Fuzhou University, Fuzhou 350108 (China); Chen Guonan, E-mail: gnchen@fzu.edu.c [Ministry of Education Key Laboratory of Analysis and Detection for Food Safety, Fujian Provincial Key Laboratory of Analysis and Detection Technology for Food Safety, Department of Chemistry, Fuzhou University, Fuzhou 350108 (China)

    2011-04-15

    Research highlights: {yields} We fabricate a polyion graphene complex membrane-based immunosensing platform for sensitive electrochemical immunoassay of alpha-fetoprotein. {yields} Nanosilver-coated silica nanocomposites as bionanolabels. {yields} Graphene nanosheets, single-stranded DNA and silver nanoparticles as matrices. {yields} Direct electron transfer without electron mediator. {yields} Analysis of real samples and method comparison. - Abstract: A facile and sensitive mediator-free electrochemical immunosensor for detection of alpha-fetoprotein (AFP) was designed by using nanosilver-coated silica nanoparticles (Ag-SiO{sub 2}) as bionanolabels. To construct such an electrochemical immunosensor, silver ions/single-stranded DNA/graphene nanosheets were initially immobilized on a gold electrode in turn, then silver ions were in situ reduced to silver nanoparticles with the aid of NaBH{sub 4}, and anti-AFP antibodies conjugated to silver nanoparticles were used. In the presence of AFP analyte, the sandwiched immunocomplex was formed on the electrode surface by using horseradish peroxidase-anti-AFP conjugate-labeled Ag-SiO{sub 2} (HRP-anti-AFP-Ag-SiO{sub 2}) as secondary antibodies. Compared with pure silver nanoparticles, Ag-SiO{sub 2} nanocomposites could provide a large room for the immobilization of HRP-anti-AFP, and improve the electrochemical responses of the immunosensor. Meanwhile, the presence of highly conductive graphene nanosheets and silver nanoparticles provided a good pathway for electron transfer. Under optimal conditions, the immunosensor exhibited good electrochemical responses toward AFP ranging from 0.3 to 200 ng/mL with a detection limit (LOD) of 0.05 ng/mL (at 3{sigma}) in pH 6.0 PBS-H{sub 2}O{sub 2} system. Intra- and inter-assay displayed good precisions with coefficient of variation below 9.5%. In addition, the method was evaluated with 23 clinical serum samples, receiving good correlation with results from commercially available

  3. Nanosilver-penetrated polyion graphene complex membrane for mediator-free amperometric immunoassay of alpha-fetoprotein using nanosilver-coated silica nanoparticles

    International Nuclear Information System (INIS)

    Tang Juan; Tang Dianping; Su Biling; Li Qunfang; Qiu Bin; Chen Guonan

    2011-01-01

    Research highlights: → We fabricate a polyion graphene complex membrane-based immunosensing platform for sensitive electrochemical immunoassay of alpha-fetoprotein. → Nanosilver-coated silica nanocomposites as bionanolabels. → Graphene nanosheets, single-stranded DNA and silver nanoparticles as matrices. → Direct electron transfer without electron mediator. → Analysis of real samples and method comparison. - Abstract: A facile and sensitive mediator-free electrochemical immunosensor for detection of alpha-fetoprotein (AFP) was designed by using nanosilver-coated silica nanoparticles (Ag-SiO 2 ) as bionanolabels. To construct such an electrochemical immunosensor, silver ions/single-stranded DNA/graphene nanosheets were initially immobilized on a gold electrode in turn, then silver ions were in situ reduced to silver nanoparticles with the aid of NaBH 4 , and anti-AFP antibodies conjugated to silver nanoparticles were used. In the presence of AFP analyte, the sandwiched immunocomplex was formed on the electrode surface by using horseradish peroxidase-anti-AFP conjugate-labeled Ag-SiO 2 (HRP-anti-AFP-Ag-SiO 2 ) as secondary antibodies. Compared with pure silver nanoparticles, Ag-SiO 2 nanocomposites could provide a large room for the immobilization of HRP-anti-AFP, and improve the electrochemical responses of the immunosensor. Meanwhile, the presence of highly conductive graphene nanosheets and silver nanoparticles provided a good pathway for electron transfer. Under optimal conditions, the immunosensor exhibited good electrochemical responses toward AFP ranging from 0.3 to 200 ng/mL with a detection limit (LOD) of 0.05 ng/mL (at 3σ) in pH 6.0 PBS-H 2 O 2 system. Intra- and inter-assay displayed good precisions with coefficient of variation below 9.5%. In addition, the method was evaluated with 23 clinical serum samples, receiving good correlation with results from commercially available electrochemiluminescent analyzer.

  4. Modification of the performance of WO3-ZrO2 catalysts by metal addition in hydrocarbon reactions

    Directory of Open Access Journals (Sweden)

    Gerardo Carlos Torres

    2012-01-01

    Full Text Available A study of the different hydrocarbon reactions over Ni doped WO3-ZrO2 catalysts was performed. Ni was found as NiO at low Ni concentration while at high Ni concentrations a small fraction was present as a metal. For both cases, Ni strongly modified total acidity and concentration of strong acid sites. In the cyclohexane dehydrogenation reaction, Ni addition promotes both benzene and methyl cyclopentane production. The hydroconversion activity (n-butane and n-octane increases with the augment of total acidity produced by Ni. The selectivity to reaction products is modified according to the acid strength distribution changes produced by Ni addition.

  5. Mechanism Of Long Term Change In Electrochrcmism Of LixWO3 Films

    Science.gov (United States)

    Nagai, Junichi; Kamimori, Tadatoshi; Mizuhashi, Mamoru

    1984-11-01

    The degradation mechanism of gradual decrease of the contrast between colored and bleached states of Lix'. WO3 films with switching cycles was investigated. We made electro-chemical and quantitative chemical analyses to clarify this phenomenon. It was found that the decrease in contrast was mostly attributed to the parallel cathodic shift of emf(x), passibly caused by ion exchange reaction expressed by: WOH + Li+ WOLi + H. Fully ion-exchanged WO3 films showed no appreciable change in spite of the presence of a large amount of Li in them. These films were capable of accepting as much Li as the fresh films did on coloration and reached to the same optical densities. It is concluded that there are two kinds of active sites available for accepting lithium ions in the WO3 structure, one for ion exchange and the other for coloration.

  6. Spontaneous synthesis of gold nanoparticles on gum arabic-modified iron oxide nanoparticles as a magnetically recoverable nanocatalyst.

    Science.gov (United States)

    Wu, Chien-Chen; Chen, Dong-Hwang

    2012-06-19

    A novel magnetically recoverable Au nanocatalyst was fabricated by spontaneous green synthesis of Au nanoparticles on the surface of gum arabic-modified Fe3O4 nanoparticles. A layer of Au nanoparticles with thickness of about 2 nm was deposited on the surface of gum arabic-modified Fe3O4 nanoparticles, because gum arabic acted as a reducing agent and a stabilizing agent simultaneously. The resultant magnetically recoverable Au nanocatalyst exhibited good catalytic activity for the reduction of 4-nitrophenol with sodium borohydride. The rate constants evaluated in terms of pseudo-first-order kinetic model increased with increase in the amount of Au nanocatalyst or decrease in the initial concentration of 4-nitrophenol. The kinetic data suggested that this catalytic reaction was diffusion-controlled, owing to the presence of gum arabic layer. In addition, this nanocatalyst exhibited good stability. Its activity had no significant decrease after five recycles. This work is useful for the development and application of magnetically recoverable Au nanocatalyst on the basis of green chemistry principles.

  7. Spontaneous synthesis of gold nanoparticles on gum arabic-modified iron oxide nanoparticles as a magnetically recoverable nanocatalyst

    Science.gov (United States)

    2012-01-01

    A novel magnetically recoverable Au nanocatalyst was fabricated by spontaneous green synthesis of Au nanoparticles on the surface of gum arabic-modified Fe3O4 nanoparticles. A layer of Au nanoparticles with thickness of about 2 nm was deposited on the surface of gum arabic-modified Fe3O4 nanoparticles, because gum arabic acted as a reducing agent and a stabilizing agent simultaneously. The resultant magnetically recoverable Au nanocatalyst exhibited good catalytic activity for the reduction of 4-nitrophenol with sodium borohydride. The rate constants evaluated in terms of pseudo-first-order kinetic model increased with increase in the amount of Au nanocatalyst or decrease in the initial concentration of 4-nitrophenol. The kinetic data suggested that this catalytic reaction was diffusion-controlled, owing to the presence of gum arabic layer. In addition, this nanocatalyst exhibited good stability. Its activity had no significant decrease after five recycles. This work is useful for the development and application of magnetically recoverable Au nanocatalyst on the basis of green chemistry principles. PMID:22713480

  8. Hydrothermal deposition and photochromic performances of three kinds of hierarchical structure arrays of WO3 thin films

    International Nuclear Information System (INIS)

    Ding, Defang; Shen, Yi; Ouyang, Yali; Li, Zhen

    2012-01-01

    Three kinds of tungsten oxide (WO 3 ) thin films have been fabricated by a simple hydrothermal deposition method. Scanning electron microscopy images of the products revealed that the capping agents did impact the microstructure of WO 3 films. Films prepared without capping agents were ordered nanorod arrays, while the ones obtained with ethanol and oxalic acid revealed peeled-orange-like and cauliflower-like hierarchical structure arrays, respectively. Both of the two hierarchical structures were composed of much thinner nanorods compared with the one obtained without capping agents. All the WO 3 films exhibited good photochromic properties and the two with inducers performed even better, which could be due to the changes in the microstructure that increased the amount of photogenerated electron–hole pairs and the proton diffusion rates. - Highlights: ► Ordered WO 3 nanorod arrays were prepared by hydrothermal deposition process. ► Two hierarchical WO 3 structure arrays were obtained with ethanol and oxalic acid. ► Mechanism for the improved photochromic performances of WO 3 films is proposed.

  9. Synthesis and optical properties of Au decorated colloidal tungsten oxide nanoparticles

    International Nuclear Information System (INIS)

    Tahmasebi, Nemat; Mahdavi, Seyed Mohammad

    2015-01-01

    Highlights: • Tungsten oxide nanoparticles were prepared by pulsed laser ablation (PLA). • A very fine metallic Au particles or coating are decorated on the surface of tungsten oxide nanoparticles. • UV–Vis spectroscopy shows an absorption peak at ∼530 nm which is due to SPR effect of gold. • After exposing to hydrogen gas, Au/WO_3 colloidal nanoparticles show excellent gasochromic coloring. - Abstract: In this study, colloidal tungsten oxide nanoparticles were fabricated by pulsed laser ablation of tungsten target using the first harmonic of a Nd:YAG laser (1064 nm) in deionized water. After ablation, a 0.33 g/lit HAuCl_4 aqueous solution was added into as-prepared colloidal nanoparticles. In this process, Au"3"+ ions were reduced to decorate gold metallic state (Au"0) onto colloidal tungsten oxide nanoparticles surface. The morphology and chemical composition of the synthesized nanoparticles were studied by AFM, XRD, TEM and XPS techniques. UV–Vis analysis reveals a distinct absorption peak at ∼530 nm. This peak can be attributed to the surface plasmon resonance (SPR) of Au and confirms formation of gold state. Moreover, X-ray photoelectron spectroscopy reveals that Au ions’ reduction happens after adding HAuCl_4 solution into as-prepared colloidal tungsten oxide nanoparticles. Transmission electron microscope shows that an Au shell has been decorated onto colloidal WO_3 nanoparticles. Noble metal decorated tungsten oxide nanostructure could be an excellent candidate for photocatalysis, gas sensing and gasochromic applications. Finally, the gasochromic behavior of the synthesized samples was investigated by H_2 and O_2 gases bubbling into the produced colloidal Au/WO_3 nanoparticles. Synthesized colloidal nanoparticles show excellent coloration contrast (∼80%) through NIR spectra.

  10. Elucidating the real-time Ag nanoparticle growth on α-Ag2WO4 during electron beam irradiation: experimental evidence and theoretical insights.

    Science.gov (United States)

    Pereira, Wyllamanney da Silva; Andrés, Juan; Gracia, Lourdes; San-Miguel, Miguel A; da Silva, Edison Z; Longo, Elson; Longo, Valeria M

    2015-02-21

    Why and how Ag is formed when electron beam irradiation takes place on α-Ag2WO4 in a vacuum transmission electron microscopy chamber? To find an answer, the atomic-scale mechanisms underlying the formation and growth of Ag on α-Ag2WO4 have been investigated by detailed in situ transmission electron microscopy (TEM) and field emission scanning electron microscopy (FE-SEM) studies, density functional theory based calculations and ab initio molecular dynamics simulations. The growth process at different times, chemical composition, size distribution and element distribution were analyzed in depth at the nanoscale level using FE-SEM, operated at different voltages (5, 10, 15, and 20 kV), and TEM with energy dispersive spectroscopy (EDS) characterization. The size of Ag nanoparticles covers a wide range of values. Most of the Ag particles are in the 20-40 nm range. The nucleation and formation of Ag on α-Ag2WO4 is a result of structural and electronic changes in the AgOx (x = 2,4, 6, and 7) clusters used as constituent building blocks of this material, consistent with metallic Ag formation. First principle calculations point out that Ag-3 and Ag-4-fold coordinated centers, located in the sub-surface of the (100) surface, are the most energetically favorable to undergo the diffusion process to form metallic Ag. Ab initio molecular dynamics simulations and the nudged elastic band (NEB) method were used to investigate the minimum energy pathways of these Ag atoms from positions in the first slab layer to outward sites on the (100) surface of α-Ag2WO4. The results point out that the injection of electrons decreases the activation barrier for this diffusion step and this unusual behavior results from the presence of a lower energy barrier process.

  11. Photovoltaic characterization of hybrid solar cells using surface modified TiO{sub 2} nanoparticles and poly(3-hexyl)thiophene

    Energy Technology Data Exchange (ETDEWEB)

    Guenes, Serap [Yildiz Technical University, Faculty of Arts and Science, Department of Physics, Davutpasa Campus, 34220, Esenler, Istanbul (Turkey); Marjanovic, Nenad [Plastic electronic GmbH, Rappetsederweg 28, A-4040 Linz (Austria); Nedeljkovic, Jovan M [Vinca Institute of Nuclear Sciences, PO Box 522, 11001 Belgrade (Serbia); Sariciftci, Niyazi Serdar [Linz Institute for Organic Solar Cells (LIOS), Physical Chemistry, Johannes Kepler University Linz, Altenberger Strasse 69, A-4040, Linz (Austria)], E-mail: sgunes@yildiz.edu.tr

    2008-10-22

    We report on the photovoltaic performance of bulk heterojunction solar cells using novel nanoparticles of 6-palmitate ascorbic acid surface modified TiO{sub 2} as an electron acceptor embedded into the donor poly(3-hexyl)thiophene (P3HT) matrix. Devices were fabricated by using P3HT with varying amounts of red TiO{sub 2} nanoparticles (1:1, 1:2, 1:3 w-w ratio). The devices were characterized by measuring current-voltage characteristics under simulated AM 1.5 conditions. Incident photon to current efficiency (IPCE) was spectrally resolved. The nanoscale morphology of such organic/inorganic hybrid blends was also investigated using atomic force microscopy (AFM)

  12. Proximity hybridization-regulated catalytic DNA hairpin assembly for electrochemical immunoassay based on in situ DNA template-synthesized Pd nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Fuyi [School of Chemistry and Chemical Engineering, Jiangsu Normal University, Xuzhou 221116 (China); Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Department of Pharmaceutical Analysis, School of Pharmacy, Xuzhou Medical College, 221004, Xuzhou (China); Yao, Yao; Luo, Jianjun; Zhang, Xing; Zhang, Yu; Yin, Dengyang [Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Department of Pharmaceutical Analysis, School of Pharmacy, Xuzhou Medical College, 221004, Xuzhou (China); Gao, Fenglei, E-mail: jsxzgfl@sina.com [Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Department of Pharmaceutical Analysis, School of Pharmacy, Xuzhou Medical College, 221004, Xuzhou (China); Wang, Po, E-mail: wangpo@jsnu.edu.cn [School of Chemistry and Chemical Engineering, Jiangsu Normal University, Xuzhou 221116 (China)

    2017-05-29

    Novel hybridization proximity-regulated catalytic DNA hairpin assembly strategy has been proposed for electrochemical immunoassay based on in situ DNA template-synthesized Pd nanoparticles as signal label. The DNA template-synthesized Pd nanoparticles were characterized with atomic force microscopic and X-ray photoelectron spectroscopy. The highly efficient electrocatalysis by DNA template synthesized Pd nanoparticles for NaBH{sub 4} oxidation produced an intense detection signal. The label-free electrochemical method achieved the detection of carcinoembryonic antigen (CEA) with a linear range from 10{sup −15} to 10{sup −11} g mL{sup −1} and a detection limit of 0.43 × 10{sup −15} g mL{sup −1}. Through introducing a supersandwich reaction to increase the DNA length, the electrochemical signal was further amplified, leading to a detection limit of 0.52 × 10{sup −16} g mL{sup −1}. And it rendered satisfactory analytical performance for the determination of CEA in serum samples. Furthermore, it exhibited good reproducibility and stability; meanwhile, it also showed excellent specificity due to the specific recognition of antigen by antibody. Therefore, the DNA template synthesized Pd nanoparticles based signal amplification approach has great potential in clinical applications and is also suitable for quantification of biomarkers at ultralow level. - Graphical abstract: A novel label-free and enzyme-free electrochemical immunoassay based on proximity hybridization-regulated catalytic DNA hairpin assemblies for recycling of the CEA. - Highlights: • A novel enzyme-free electrochemical immunosensor was developed for detection of CEA. • The signal amplification was based on catalytic DNA hairpin assembly and DNA-template-synthesized Pd nanoparticles. • The biosensor could detect CEA down to 0.52 × 10{sup −16} g mL{sup −1} level with a dynamic range spanning 5 orders of magnitude.

  13. Oriented antibody immobilization to polystyrene macrocarriers for immunoassay modified with hydrazide derivatives of poly(methacrylic acid

    Directory of Open Access Journals (Sweden)

    Vinokurova Ludmila G

    2001-08-01

    Full Text Available Abstract Background Hydrophobic polystyrene is the most common material for solid phase immunoassay. Proteins are immobilized on polystyrene by passive adsorption, which often causes considerable denaturation. Biological macromolecules were found to better retain their functional activity when immobilized on hydrophilic materials. Polyacrylamide is a common material for solid-phase carriers of biological macromolecules, including immunoreagents used in affinity chromatography. New macroformats for immunoassay modified with activated polyacrylamide derivatives seem to be promising. Results New polymeric matrices for immunoassay in the form of 0.63-cm balls which contain hydrazide functional groups on hydrophilic polymer spacer arms at their surface shell are synthesized by modification of aldehyde-containing polystyrene balls with hydrazide derivatives of poly(methacrylic acid. The beads contain up to 0.31 μmol/cm2 active hydrazide groups accessible for covalent reaction with periodate-oxidized antibodies. The matrices obtained allow carrying out the oriented antibody immobilization, which increases the functional activity of immunosorbents. Conclusions An efficient site-directed antibody immobilization on a macrosupport is realized. The polymer hydrophilic spacer arms are the most convenient and effective tools for oriented antibody coupling with molded materials. The suggested scheme can be used for the modification of any other solid supports containing electrophilic groups reacting with hydrazides.

  14. Synthesis and Characterization of WO3/Graphene Nanocomposites for Enhanced Photocatalytic Activities by One-Step In-Situ Hydrothermal Reaction

    Directory of Open Access Journals (Sweden)

    Xiaoxiao Hu

    2018-01-01

    Full Text Available Tungsten trioxide (WO3 nanorods are synthesized on the surface of graphene (GR sheets by using a one-step in-situ hydrothermal method employing sodium tungstate (Na2WO4·2H2O and graphene oxide (GO as precursors. The resulting WO3/GR nanocomposites are characterized by X-ray diffraction, Raman spectroscopy, transmission electron microscopy, scanning electron microscopy and X-ray photoelectron spectroscopy. The results confirm that the interface between WO3 nanorod and graphene contains chemical bonds. The enhanced optical absorption properties are measured by UV-vis diffuse reflectance spectra. The photocatalytic activity of the WO3/GR nanocomposites under visible light is evaluated by the photodegradation of methylene blue, where the degradation rate of WO3/GR nanocomposites is shown to be double that of pure WO3. This is attributed to the synergistic effect of graphene and the WO3 nanorod, which greatly enhances the photocatalytic performance of the prepared sample, reduces the recombination of the photogenerated electron-hole pairs and increases the visible light absorption efficiency. Finally, the photocatalytic mechanism of the WO3/GR nanocomposites is presented. The synthesis of the prepared sample is convenient, direct and environmentally friendly. The study reports a highly efficient composite photocatalyst for the degradation of contaminants that can be applied to cleaning up the environment.

  15. Defect engineering of two-dimensional WO{sub 3} nanosheets for enhanced electrochromism and photoeletrochemical performance

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Xiaofang; Zheng, Xiaoli; Yan, Bo; Xu, Tao; Xu, Qun, E-mail: qunxu@zzu.edu.cn

    2017-04-01

    Highlights: • We establish a facile strategy by solvothermal reaction and hydrogenation to synthesize 2D WO{sub 3} ultrathin nanosheets with abundant oxygen vacancies. • We find that the hydrogenated WO{sub 3} ultrathin nanosheets exhibit outstanding electrochromism properties. • Moreover, the hydrogenated WO{sub 3} nanosheets also exhibit remarkable photocatalytic performance. • The outstanding electrochromism and photoelectrochemical performances are mainly due to increased oxygen vacancies and narrowed band gap. - Abstract: The capability of introduction of oxygen vacancies in a controlled way has emerged as the heart of modern transition metal oxide semiconductor chemistry. As chemical defects, the oxygen vacancies have been proposed as electron donors, which are prone to increase carrier density and promote charge carrier separation. Herein, we have successfully prepared 2D WO{sub 3} ultrathin nanosheets with abundant surface oxygen vacancies by a combination of facile solvothermal reaction and hydrogenation method. The resultant hydrogenated WO{sub 3} ultrathin nanosheets exhibit remarkable electrochromism and photocatalytic performances compared with the non-hydrogenated samples, mainly due to their increased oxygen vacancies, narrowed band gap coupled with fast charge transfer and enhanced adsorption of visible light.

  16. A study of transition from n- to p-type based on hexagonal WO3 nanorods sensor

    Science.gov (United States)

    Wu, Ya-Qiao; Hu, Ming; Wei, Xiao-Ying

    2014-04-01

    Hexagonal WO3 nanorods are fabricated by a facile hydrothermal process at 180 °C using sodium tungstate and sodium chloride as starting materials. The morphology, structure, and composition of the prepared nanorods are studied by scanning electron microscopy, X-ray diffraction spectroscopy, and energy dispersive spectroscopy. It is found that the agglomeration of the nanorods is strongly dependent on the PH value of the reaction solution. Uniform and isolated WO3 nanorods with diameters ranging from 100 nm-150 nm and lengths up to several micrometers are obtained at PH = 2.5 and the nanorods are identified as being hexagonal in phase structure. The sensing characteristics of the WO3 nanorod sensor are obtained by measuring the dynamic response to NO2 with concentrations in the range 0.5 ppm-5 ppm and at working temperatures in the range 25 °C-250 °C. The obtained WO3 nanorods sensors are found to exhibit opposite sensing behaviors, depending on the working temperature. When being exposed to oxidizing NO2 gas, the WO3 nanorod sensor behaves as an n-type semiconductor as expected when the working temperature is higher than 50 °C, whereas, it behaves as a p-type semiconductor below 50 °C. The origin of the n- to p-type transition is correlated with the formation of an inversion layer at the surface of the WO3 nanorod at room temperature. This finding is useful for making new room temperature NO2 sensors based on hexagonal WO3 nanorods.

  17. A study of transition from n- to p-type based on hexagonal WO3 nanorods sensor

    International Nuclear Information System (INIS)

    Wu Ya-Qiao; Hu Ming; Wei Xiao-Ying

    2014-01-01

    Hexagonal WO 3 nanorods are fabricated by a facile hydrothermal process at 180 °C using sodium tungstate and sodium chloride as starting materials. The morphology, structure, and composition of the prepared nanorods are studied by scanning electron microscopy, X-ray diffraction spectroscopy, and energy dispersive spectroscopy. It is found that the agglomeration of the nanorods is strongly dependent on the PH value of the reaction solution. Uniform and isolated WO 3 nanorods with diameters ranging from 100 nm–150 nm and lengths up to several micrometers are obtained at PH = 2.5 and the nanorods are identified as being hexagonal in phase structure. The sensing characteristics of the WO 3 nanorod sensor are obtained by measuring the dynamic response to NO 2 with concentrations in the range 0.5 ppm–5 ppm and at working temperatures in the range 25 °C–250 °C. The obtained WO 3 nanorods sensors are found to exhibit opposite sensing behaviors, depending on the working temperature. When being exposed to oxidizing NO 2 gas, the WO 3 nanorod sensor behaves as an n-type semiconductor as expected when the working temperature is higher than 50 °C, whereas, it behaves as a p-type semiconductor below 50 °C. The origin of the n- to p-type transition is correlated with the formation of an inversion layer at the surface of the WO 3 nanorod at room temperature. This finding is useful for making new room temperature NO 2 sensors based on hexagonal WO 3 nanorods. (general)

  18. Hydrothermal synthesis of hierarchical WO{sub 3} nanostructures for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Rashad, M.M. [Central Metallurgical Research and Development Institute (CMRDI), Helwan, P.O. Box 87, Cairo (Egypt); Shalan, A.E. [Central Metallurgical Research and Development Institute (CMRDI), Helwan, P.O. Box 87, Cairo (Egypt); Friedrich-Alexander-University of Erlangen-Nuremberg, Institute of Materials for Electronics and Energy Technology (i-MEET), Erlangen (Germany)

    2014-08-15

    Hierarchical architectures consisting of one-dimensional (1D) nanostructures are of great interest for potential use in energy and environmental applications in recent years. In this work, hierarchical tungsten oxide (WO{sub 3}) has been synthesized via a facile hydrothermal route from ammonium metatungstate hydrate and implemented as photoelectrode for dye-sensitized solar cells. The urchin-like WO{sub 3} micro-patterns are constructed by self-organized nanoscale length 1D building blocks, which are single crystalline in nature, grown along (001) direction and confirm an orthorhombic crystal phase. The obtained powders were investigated by XRD, SEM, TEM and UV-Vis Spectroscopy. The photovoltaic performance of dye-sensitized solar cells based on WO{sub 3} photoanodes was investigated. With increasing the calcination temperature of the prepared nanopowders, the light-electricity conversion efficiency (η) was increased. The results were attributed to increase the crystallinity of the particles and ease of electron movement. The DSSC based on hierarchical WO{sub 3} showed a short-circuit current, an open-circuit voltage, a fill factor, and a conversion efficiency of 4.241 mA/cm{sup 2}, 0.656 V, 66.74, and 1.85 %, respectively. (orig.)

  19. Synthesis, structure characterization and catalytic activity of nickel tungstate nanoparticles

    International Nuclear Information System (INIS)

    Pourmortazavi, Seied Mahdi; Rahimi-Nasrabadi, Mehdi; Khalilian-Shalamzari, Morteza; Zahedi, Mir Mahdi; Hajimirsadeghi, Seiedeh Somayyeh; Omrani, Ismail

    2012-01-01

    Graphical abstract: NiWO 4 nanoparticles were prepared via precipitation technique. Experimental parameters of procedure were optimized statistically. Highlights: ► NiWO 4 spherical nanoparticles were synthesized via direct precipitation method. ► Taguchi robust design was used for optimization of synthesis reaction parameters. ► Composition and structural properties of NiWO 4 nanoparticles were characterized. ► EDAX, XRD, SEM, FT-IR, UV–vis and photoluminescence techniques were employed. ► Catalytic activity of the product in a cyclo-addition reaction was investigated. - Abstract: Taguchi robust design was applied to optimize experimental parameters for controllable, simple and fast synthesis of nickel tungstate nanoparticles. NiWO 4 nanoparticles were synthesized by precipitation reaction involving addition of nickel ion solution to the tungstate aqueous reagent and then formation of nickel tungstate nucleolus which are insoluble in aqueous media. Effects of various parameters such as nickel and tungstate concentrations, flow rate of reagent addition and reactor temperature on diameter of synthesized nickel tungstate nanoparticles were investigated experimentally by the aid of orthogonal array design. The results for analysis of variance (ANOVA) showed that particle size of nickel tungstate can be effectively tuned by controlling significant variables involving nickel and tungstate concentrations and flow rate; while, temperature of the reactor has a no considerable effect on the size of NiWO 4 particles. The ANOVA results proposed the optimum conditions for synthesis of nickel tungstate nanoparticles via this technique. Also, under optimum condition nanoparticles of NiWO 4 were prepared and their structure and chemical composition were characterized by means of EDAX, XRD, SEM, FT-IR spectroscopy, UV–vis spectroscopy, and photoluminescence. Finally, catalytic activity of the nanoparticles in a cycloaddition reaction was examined.

  20. Synthesis, structure characterization and catalytic activity of nickel tungstate nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Pourmortazavi, Seied Mahdi, E-mail: pourmortazavi@yahoo.com [Faculty of Material and Manufacturing Technologies, Malek Ashtar University of Technology, Tehran (Iran, Islamic Republic of); Rahimi-Nasrabadi, Mehdi, E-mail: rahiminasrabadi@gmail.com [Department of Chemistry, Imam Hossein University, Tehran (Iran, Islamic Republic of); Khalilian-Shalamzari, Morteza [Department of Chemistry, Imam Hossein University, Tehran (Iran, Islamic Republic of); Zahedi, Mir Mahdi; Hajimirsadeghi, Seiedeh Somayyeh [Islamic Azad University, Varamin Pishva Branch, Varamin (Iran, Islamic Republic of); Omrani, Ismail [Department of Chemistry, Imam Hossein University, Tehran (Iran, Islamic Republic of)

    2012-12-15

    Graphical abstract: NiWO{sub 4} nanoparticles were prepared via precipitation technique. Experimental parameters of procedure were optimized statistically. Highlights: Black-Right-Pointing-Pointer NiWO{sub 4} spherical nanoparticles were synthesized via direct precipitation method. Black-Right-Pointing-Pointer Taguchi robust design was used for optimization of synthesis reaction parameters. Black-Right-Pointing-Pointer Composition and structural properties of NiWO{sub 4} nanoparticles were characterized. Black-Right-Pointing-Pointer EDAX, XRD, SEM, FT-IR, UV-vis and photoluminescence techniques were employed. Black-Right-Pointing-Pointer Catalytic activity of the product in a cyclo-addition reaction was investigated. - Abstract: Taguchi robust design was applied to optimize experimental parameters for controllable, simple and fast synthesis of nickel tungstate nanoparticles. NiWO{sub 4} nanoparticles were synthesized by precipitation reaction involving addition of nickel ion solution to the tungstate aqueous reagent and then formation of nickel tungstate nucleolus which are insoluble in aqueous media. Effects of various parameters such as nickel and tungstate concentrations, flow rate of reagent addition and reactor temperature on diameter of synthesized nickel tungstate nanoparticles were investigated experimentally by the aid of orthogonal array design. The results for analysis of variance (ANOVA) showed that particle size of nickel tungstate can be effectively tuned by controlling significant variables involving nickel and tungstate concentrations and flow rate; while, temperature of the reactor has a no considerable effect on the size of NiWO{sub 4} particles. The ANOVA results proposed the optimum conditions for synthesis of nickel tungstate nanoparticles via this technique. Also, under optimum condition nanoparticles of NiWO{sub 4} were prepared and their structure and chemical composition were characterized by means of EDAX, XRD, SEM, FT-IR spectroscopy, UV

  1. Detection of Salmonella typhi utilizing bioconjugated fluorescent polymeric nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Jain, Swati, E-mail: swatijain.iitd@gmail.com; Chattopadhyay, Sruti, E-mail: sruticiitd@gmail.com; Jackeray, Richa; Abid, Zainul; Singh, Harpal, E-mail: harpal2000@yahoo.com [Centre for Biomedical Engineering, Indian Institute of Technology-Delhi (India)

    2016-05-15

    Present work demonstrates effective utilization of functionalized polymeric fluorescent nanoparticles as biosensing probe for the detection of Salmonella typhi bacteria on modified polycarbonate (PC) filters in about 3 h. Antibody modified-PC membranes were incubated with contaminated bacterial water for selective capturing which were detected by synthesized novel bioconjugate probe. Core–shell architecture of polymeric nanoparticles endows them with aqueous stabilization and keto-enolic functionalities making them usable for covalently linking S. typhi antibodies without any crosslinker or activator. Bradford analysis revealed that one nanoparticle has an average of 3.51 × 10{sup −19} g or 21 × 10{sup 4} bound S. typhi Ab molecules. Analysis of the regions of interest (ROI) in fluorescent micrographs of modified fluoroimmunoassay showed higher detection sensitivity of 5 × 10{sup 2} cells/mL due to signal amplification unlike conventional naked dye FITC-Ab conjugate. Fluorescence of pyrene dye remained same on immobilization of biomolecules and nanoparticles showed stable fluorescent intensity under prolong exposure to laser owing to protective polymeric layer allowing accurate identification of bacteria. Surface-functionalized PC matrix and fluorescent label NPs permit covalent interactions among biomolecules enhancing signal acquisitions showing higher detection efficiency as compared to conventional microtiter plate-based system. Our novel immunoassay has the potential to be explored as rapid detection method for identifying S. typhi contaminations in water.Graphical Abstract.

  2. Detection of Salmonella typhi utilizing bioconjugated fluorescent polymeric nanoparticles

    International Nuclear Information System (INIS)

    Jain, Swati; Chattopadhyay, Sruti; Jackeray, Richa; Abid, Zainul; Singh, Harpal

    2016-01-01

    Present work demonstrates effective utilization of functionalized polymeric fluorescent nanoparticles as biosensing probe for the detection of Salmonella typhi bacteria on modified polycarbonate (PC) filters in about 3 h. Antibody modified-PC membranes were incubated with contaminated bacterial water for selective capturing which were detected by synthesized novel bioconjugate probe. Core–shell architecture of polymeric nanoparticles endows them with aqueous stabilization and keto-enolic functionalities making them usable for covalently linking S. typhi antibodies without any crosslinker or activator. Bradford analysis revealed that one nanoparticle has an average of 3.51 × 10"−"1"9 g or 21 × 10"4 bound S. typhi Ab molecules. Analysis of the regions of interest (ROI) in fluorescent micrographs of modified fluoroimmunoassay showed higher detection sensitivity of 5 × 10"2 cells/mL due to signal amplification unlike conventional naked dye FITC-Ab conjugate. Fluorescence of pyrene dye remained same on immobilization of biomolecules and nanoparticles showed stable fluorescent intensity under prolong exposure to laser owing to protective polymeric layer allowing accurate identification of bacteria. Surface-functionalized PC matrix and fluorescent label NPs permit covalent interactions among biomolecules enhancing signal acquisitions showing higher detection efficiency as compared to conventional microtiter plate-based system. Our novel immunoassay has the potential to be explored as rapid detection method for identifying S. typhi contaminations in water.Graphical Abstract

  3. Photoelectrochemical Properties and Behavior of α-SnWO4 Photoanodes Synthesized by Hydrothermal Conversion of WO3 Films.

    Science.gov (United States)

    Zhu, Zhehao; Sarker, Pranab; Zhao, Chenqi; Zhou, Lite; Grimm, Ronald L; Huda, Muhammad N; Rao, Pratap M

    2017-01-18

    Metal oxides with moderate band gaps are desired for efficient production of hydrogen from sunlight and water via photoelectrochemical (PEC) water splitting. Here, we report an α-SnWO 4 photoanode synthesized by hydrothermal conversion of WO 3 films that achieves photon to current conversion at wavelengths up to 700 nm (1.78 eV). This photoanode is promising for overall PEC water-splitting because the flat-band potential and voltage of photocurrent onset are more negative than the potential of hydrogen evolution. Furthermore, the photoanode utilizes a large portion of the solar spectrum. However, the photocurrent density reaches only a small fraction of that which is theoretically possible. Density functional theory based thermodynamic and electronic structure calculations were performed to elucidate the nature and impact of defects in α-SnWO 4 prepared by this synthetic route, from which hole localization at Sn-at-W antisite defects was determined to be a likely cause for the poor photocurrent. Measurements further showed that the photocurrent decreases over time due to surface oxidation, which was suppressed by improving the kinetics of hole transfer at the semiconductor/electrolyte interface. Alternative synthetic methods and the addition of protective coatings and/or oxygen evolution catalysts are suggested to improve the PEC performance and stability of this promising α-SnWO 4 material.

  4. Hydrogenation of carbon monoxide on WO/sub 3/-Supported ruthenium catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Yoshinari, Tomohiro; Suganuma, Fujio; Sera, Chikara

    1988-01-01

    In this study, a WO/sub 3/-supported catalyst was prepared to conduct hydrogenation of CO for examining the product distribution and composition of hydrocarbons, using a gamma-alumina-supported catalyst for comparison. These catalysts were used under pressure to conduct a distributive reaction and the desorbing behavior of CO or H/sub 2/ at elevated temperature was measured to examine the influence of the type of carrier or the method of preparation on the activity and the distribution of products formed. The WO/sub 3/-supported catalyst gave a carbon chain length distribution that did not comply with the rule of Schulz-Flory, giving a composition richer in the isomers. Carbon number distribution is affected by Ru-dispersion, and the selectivity of isomers depends on the acidity of the carrier. Formed products distribution of the WO/sub 3/-supported reaction is attributable to the secondary reaction, which relates to the acidic point of the carrier, of the primary product formed on the metal. (7 figs, 4 tabs, 18 refs)

  5. An amperometric hydrogen peroxide biosensor based on Co3O4 nanoparticles and multiwalled carbon nanotube modified glassy carbon electrode

    International Nuclear Information System (INIS)

    Kaçar, Ceren; Dalkiran, Berna; Erden, Pınar Esra; Kiliç, Esma

    2014-01-01

    Highlights: • Hydrogen peroxide biosensor was constructed by combining the advantageous properties of MWCNTs and Co 3 O 4 . • Incorporating Co 3 O 4 nanoparticles into MWCNTs/gelatin film increased the electron transfer. • Co 3 O 4 /MWCNTs/gelatin/HRP/Nafion/GCE showed strong anti-interference ability. • Hydrogen peroxide was successfully determined in disinfector with an average recovery of 100.78 ± 0.89. - Abstract: In this work a new type of hydrogen peroxide biosensor was fabricated based on the immobilization of horseradish peroxidase (HRP) by cross-linking on a glassy carbon electrode (GCE) modified with Co 3 O 4 nanoparticles, multiwall carbon nanotubes (MWCNTs) and gelatin. The introduction of MWCNTs and Co 3 O 4 nanoparticles not only enhanced the surface area of the modified electrode for enzyme immobilization but also facilitated the electron transfer rate, resulting in a high sensitivity of the biosensor. The fabrication process of the sensing surface was characterized by scanning electron microscopy (SEM), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Amperometric detection of hydrogen peroxide was investigated by holding the modified electrode at −0.30 V (vs. Ag/AgCl). The biosensor showed optimum response within 5 s at pH 7.0. The optimized biosensor showed linear response range of 7.4 × 10 −7 –1.9 × 10 −5 M with a detection limit of 7.4 × 10 −7 . The applicability of the purposed biosensor was tested by detecting hydrogen peroxide in disinfector samples. The average recovery was calculated as 100.78 ± 0.89

  6. Solvent directed morphologies and enhanced luminescent properties of BaWO4:Tm3+,Dy3+ for white light emitting diodes

    Science.gov (United States)

    Wu, Hongyue; Yang, Junfeng; Wang, Xiaoxue; Gan, Shucai; Li, Linlin

    2018-05-01

    A series of Tm3+ and Dy3+ codoped BaWO4 phosphors with tunable shapes were controllably synthesized by a facile solvothermal method. The effects of ratio of ethylene glycol (EG) and water on the morphologies of BaWO4 structures are systematically studied. It was discovered that the reason for these morphological changes is based on the reaction speed of the kinetic control, which relates to the strong chelating abilities of ethylene glycol. And when the solvent is pure ethylene glycol, the peanut-like BaWO4:Dy3+ has the strongest emission intensity. Moreover, the emission color of the phosphors varied from blue (0.232, 0.180) to white (0.268, 0.250) by controlling Dy3+ ions content with a fixed Tm3+ concentration. The energy transfer mechanism was investigated in detail. With increasing the doped concentration of Dy3+ ions, the energy transfer efficiency of BaWO4:0.005Tm3+,yDy3+ increased gradually and reached as high as 63% when the Dy3+ doped concentration is 0.03. The critical distance RC calculated by the spectral overlap method is about 19.93 Å, and it is in good agreement with that obtained using the concentration quenching method (19.70 Å), indicating that the electric dipole-dipole interaction is the main energy transfer mechanism for BaWO4:Tm3+,Dy3+ phosphors.

  7. Correlation between excited d-orbital electron lifetime in polaron dynamics and coloration of WO3 upon ultraviolet exposure

    Science.gov (United States)

    Lee, Young-Ahn; Han, Seung-Ik; Rhee, Hanju; Seo, Hyungtak

    2018-05-01

    Polarons have been suggested to explain the mechanism of the coloration of WO3 induced by UV light. However, despite the many experimental results that support small polarons as a key mechanism, direct observation of the carrier dynamics of polarons have yet to be reported. Here, we investigate the correlation between the electronic structure and the coloration of WO3 upon exposure to UV light in 5% H2/N2 gas and, more importantly, reveal photon-induced excited d-electron generation/relaxation via the W5+ oxidation state. The WO3 is fabricated by radio-frequency magnetron sputtering. X-ray diffraction patterns show that prepared WO3 is amorphous. Optical bandgap of 3.1 eV is measured by UV-vis before and after UV light. The results of Fourier transform infrared and Raman exhibit pristine WO3 is formed with surface H2O. The colored WO3 shows reduced state of W5+ state (34.3 eV) by using X-ray photoelectron spectroscopy. The valence band maximum of WO3 after UV light in H2 is shifted from mid gap to shallow donor by using ultraviolet photoelectron spectroscopy. During the exploration of the carrier dynamics, pump (700 nm)-probe (1000 nm) spectroscopy at the femtosecond scale was used. The results indicated that electron-phonon relaxation of UV-irradiated WO3, which is the origin of the polaron-induced local surface plasmonic effect, is dominant, resulting in slow decay (within a few picoseconds); in contrast, pristine WO3 shows fast decay (less than a picosecond). Accordingly, the long photoinduced carrier relaxation is ascribed to the prolonged hot-carrier lifetime in reduced oxides resulting in a greater number of free d-electrons and, therefore, more interactions with the W5+ sub-gap states.

  8. Phase modification and surface plasmon resonance of Au/WO{sub 3} system

    Energy Technology Data Exchange (ETDEWEB)

    Bose, R. Jolly; Kavitha, V.S. [Department of Optoelectronics, University of Kerala, Kariyavattom, Thiruvananthapuram 691574, Kerala (India); Sudarsanakumar, C. [School of Pure and Applied Physics, Mahatma Gandhi University, Priyadarshini Hills, Kottayam 686560, Kerala (India); Pillai, V.P. Mahadevan, E-mail: vpmpillai9@gmail.com [Department of Optoelectronics, University of Kerala, Kariyavattom, Thiruvananthapuram 691574, Kerala (India)

    2016-08-30

    Highlights: • We have investigated the role of gold as catalyst and nucleation centers, for the crystallization and phase modification of tungsten oxide, in Au/WO{sub 3} matrix. • The phase change from triclinic WO{sub 3} to monoclinic W{sub 18}O{sub 49} is found to enhance with gold incorporation. • The surface plasmon resonance is observed in gold/tungsten oxide system with the appearance of an absorption band near the wavelength 604 nm. - Abstract: We report the action of gold as catalyst for the modification of phase from triclinic WO{sub 3} to monoclinic W{sub 18}O{sub 49} and nucleation centre for the formation of W{sub 18}O{sub 49} phase, in gold incorporated tungsten oxide films prepared by RF magnetron sputtering technique. A new band is observed near 925 cm{sup −1} in the Raman spectra of gold incorporated tungsten oxide films which is not observed in the pure tungsten oxide film. The intensity of this band enhances with gold content. A localized surface plasmon resonance (LSPR) band is observed near the wavelength 604 nm in gold incorporated tungsten oxide films. The integrated intensities of LSPR band and Raman band (∼925 cm{sup −1}) can be used for sensing the quantity of gold in the Au/WO{sub 3} matrix.

  9. Synthesis of lanthanum tungstate interconnecting nanoparticles by high voltage electrospinning

    Energy Technology Data Exchange (ETDEWEB)

    Keereeta, Yanee, E-mail: ynkeereeta@gmail.com [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Thongtem, Titipun, E-mail: ttpthongtem@yahoo.com [Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Thongtem, Somchai [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand)

    2015-10-01

    Graphical abstract: - Highlights: • La{sub 2}(WO{sub 4}){sub 3} as one of semiconducting materials. • H.V. electrospinning was used to synthesize La{sub 2}(WO{sub 4}){sub 3} interconnecting nanoparticles. • A promising material for photoemission. - Abstract: Lanthanum tungstate (La{sub 2}(WO{sub 4}){sub 3}) interconnecting nanoparticles in the shape of fibers were successfully synthesized by electrospinning in combination with high temperature calcination. In this research, calcination temperature for the synthesis of the fibers evidently influenced the diameter, morphology and crystalline degree. The crystalline monoclinic La{sub 2}(WO{sub 4}){sub 3} fibers with 200–700 nm in diameter, two main Raman peaks at 945 and 927 cm{sup −1}, FTIR stretching modes at 936 and 847 cm{sup −1}, 2.02 eV energy gap and 415–430 nm blue emission were synthesized by calcination of inorganic/organic hybrid fibers at 750 °C for 5 h, characterized by X-ray diffraction, scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, UV–visible spectroscopy and photoluminescence (PL) spectroscopy. The surface of the composite fibers before calcination was very smooth. Upon calcination the composite fibers at 750 °C for 5 h, they were transformed into nanoparticles join together in the shape of fibers with rough surface.

  10. Immunoassay for serum amyloid A using a glassy carbon electrode modified with carboxy-polypyrrole, multiwalled carbon nanotubes, ionic liquid and chitosan

    International Nuclear Information System (INIS)

    Xia, Chunyong; Li, Yuan; Yuan, Guolin; Guo, Yanlei; Yu, Chao

    2015-01-01

    We report on a highly sensitive electrochemical immunoassay for the serum inflammation marker amyloid A (SAA). It is making use of a glassy carbon electrode that was modified with carboxy-endcapped polypyrrole (PPy-α-COOH), multiwalled carbon nanotubes (MWCNTs), ionic liquid and chitosan acting as the support platform. The nanocomposite increases the sensitivity and stability of the assay. Antibody against SAA was immobilized on a monolayer surface consisting of PPy-α-COOH. The electrode material was characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectra, cyclic voltammetry, electrochemical impedance spectroscopy and differential pulse voltammetry. The calibration plot for this assay, when operated at 0.16 V (vs. SCE) and applied to spiked serum samples, is linear in the 0.001 to 900 ng mL −1 SAA concentration range, and the detection limit is as low as 0.3 pg mL −1 (at an S/N ratio of 3). The electrode is stable and highly sensitive. The detection scheme is likely to be applicable to numerous other kinds of immunoassays. (author)

  11. Gd{sub 2}O{sub 3} nanoparticles stabilized by hydrothermally modified dextrose for positive contrast magnetic resonance imaging

    Energy Technology Data Exchange (ETDEWEB)

    Babić-Stojić, Branka, E-mail: babic@vinca.rs [Vinča Institute of Nuclear Sciences, University of Belgrade, PO Box 522, 11001 Belgrade (Serbia); Jokanović, Vukoman; Milivojević, Dušan [Vinča Institute of Nuclear Sciences, University of Belgrade, PO Box 522, 11001 Belgrade (Serbia); Požek, Miroslav [Department of Physics, Faculty of Science, University of Zagreb, 10000 Zagreb (Croatia); Jagličić, Zvonko [Institute of Mathematics, Physics and Mechanics, Jadranska 19, 1000 Ljubljana (Slovenia); Makovec, Darko [Department for Materials Synthesis, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Arsikin, Katarina; Paunović, Verica [Institute of Microbiology and Immunology, School of Medicine, University of Belgrade, 11000 Belgrade (Serbia)

    2016-04-01

    Gd{sub 2}O{sub 3} nanoparticles of a few nm in size and their agglomerates dispersed in dextrose derived polymer template were synthesized by hydrothermal treatment. The produced nanosized material was investigated by TEM, FTIR spectroscopy, SQUID measurements and NMR relaxometry. Biological evaluation of this material was done by crystal violet and MTT assays to determine the cell viability. Longitudinal and transverse NMR relaxivities of water diluted Gd{sub 2}O{sub 3} nanoparticle dispersions measured at the magnetic field of 1.5 T, estimated to be r{sub 1}(Gd{sub 2}O{sub 3})=9.6 s{sup −1} mM{sup −1} in the Gd concentration range 0.1–30 mM and r{sub 2}(Gd{sub 2}O{sub 3})=17.7 s{sup −1} mM{sup −1} in the lower concentration range 0.1–0.8 mM, are significantly higher than the corresponding relaxivities measured for the standard contrast agent r{sub 1}(Gd-DTPA)=4.1 s{sup −1} mM{sup −1} and r{sub 2}(Gd-DTPA)=5.1 s{sup −1} mM{sup −1}. The ratio of the two relaxivities for Gd{sub 2}O{sub 3} nanoparticles r{sub 2}/r{sub 1}=1.8 is suitable for T{sub 1}-weighted imaging. Good MRI signal intensities of the water diluted Gd{sub 2}O{sub 3} nanoparticle dispersions were recorded at lower Gd concentrations 0.2–0.8 mM. The Gd{sub 2}O{sub 3} samples did not exert any significant cytotoxic effects at Gd concentrations of 0.2 mM and below. These properties of the produced Gd{sub 2}O{sub 3} nanoparticles in hydrothermally modified dextrose make them promising for potential application in MRI for the design of a positive MRI contrast agent. - Highlights: • Gd{sub 2}O{sub 3} nanoparticles (NPs) were stabilized by hydrothermally modified dextrose. • Magnetic moment per Gd{sup 3+} ion in the Gd{sub 2}O{sub 3} NPs is much lower than that in the bulk. • The ratio r{sub 2}/r{sub 1}=1.8 for Gd{sub 2}O{sub 3} NPs dispersions is favorable for T{sub 1}-weighted MRI. • Gd{sub 2}O{sub 3} NPs dispersions had good MRI signal intensity just at lower Gd concentrations

  12. Electrochromism and photocatalysis in dendrite structured Ti:WO3 thin films grown by sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Karuppasamy, A., E-mail: karuppasamy@psnacet.edu.in

    2015-12-30

    Graphical abstract: - Highlights: • Dendrite structured Ti doped WO{sub 3} (WTO) thin films are grown by co-sputtering. • Sputtering condition influences structure and surface morphology of WTO films. • Titanium doping and annealing lead to dendritic surface structures in WTO films. • Structural, optical, electrochromic and photocatalytic properties of WTO films. • Enhanced electrochromism and photocatalysis in dendrite structured WTO thin films. - Abstract: Titanium doped tungsten oxide (Ti:WO{sub 3}) thin films with dendrite surface structures were grown by co-sputtering titanium and tungsten in Ar + O{sub 2} atmosphere. Ti:WO{sub 3} thin films were deposited at oxygen flow rates corresponding to pressures in the range 1.0 × 10{sup −3}–5.0 × 10{sup −3} mbar. Argon flow rate and sputtering power densities for titanium (2 W/cm{sup 2}) and tungsten (3 W/cm{sup 2}) were kept constant. Ti:WO{sub 3} films deposited at an oxygen pressure of 5 × 10{sup −3} mbar are found to be better electrochromic and photocatalytic. They have high optical modulation (80% at λ = 550 nm), coloration efficiency (60 cm{sup 2}/C at λ = 550 nm), electron/ion storage and removal capacity (Qc: −22.01 mC/cm{sup 2}, Qa: 17.72 mC/cm{sup 2}), reversibility (80%) and methylene blue decomposition rate (−1.38 μmol/l d). The combined effects of titanium doping, dendrite surface structures and porosity leads to significant enhancement in the electrochromic and photocatalytic properties of Ti:WO{sub 3} films.

  13. Electrochromism and photocatalysis in dendrite structured Ti:WO3 thin films grown by sputtering

    International Nuclear Information System (INIS)

    Karuppasamy, A.

    2015-01-01

    Graphical abstract: - Highlights: • Dendrite structured Ti doped WO 3 (WTO) thin films are grown by co-sputtering. • Sputtering condition influences structure and surface morphology of WTO films. • Titanium doping and annealing lead to dendritic surface structures in WTO films. • Structural, optical, electrochromic and photocatalytic properties of WTO films. • Enhanced electrochromism and photocatalysis in dendrite structured WTO thin films. - Abstract: Titanium doped tungsten oxide (Ti:WO 3 ) thin films with dendrite surface structures were grown by co-sputtering titanium and tungsten in Ar + O 2 atmosphere. Ti:WO 3 thin films were deposited at oxygen flow rates corresponding to pressures in the range 1.0 × 10 −3 –5.0 × 10 −3 mbar. Argon flow rate and sputtering power densities for titanium (2 W/cm 2 ) and tungsten (3 W/cm 2 ) were kept constant. Ti:WO 3 films deposited at an oxygen pressure of 5 × 10 −3 mbar are found to be better electrochromic and photocatalytic. They have high optical modulation (80% at λ = 550 nm), coloration efficiency (60 cm 2 /C at λ = 550 nm), electron/ion storage and removal capacity (Qc: −22.01 mC/cm 2 , Qa: 17.72 mC/cm 2 ), reversibility (80%) and methylene blue decomposition rate (−1.38 μmol/l d). The combined effects of titanium doping, dendrite surface structures and porosity leads to significant enhancement in the electrochromic and photocatalytic properties of Ti:WO 3 films.

  14. Materials for Microfluidic Immunoassays: A Review.

    Science.gov (United States)

    Mou, Lei; Jiang, Xingyu

    2017-08-01

    Conventional immunoassays suffer from at least one of these following limitations: long processing time, high costs, poor user-friendliness, technical complexity, poor sensitivity and specificity. Microfluidics, a technology characterized by the engineered manipulation of fluids in channels with characteristic lengthscale of tens of micrometers, has shown considerable promise for improving immunoassays that could overcome these limitations in medical diagnostics and biology research. The combination of microfluidics and immunoassay can detect biomarkers with faster assay time, reduced volumes of reagents, lower power requirements, and higher levels of integration and automation compared to traditional approaches. This review focuses on the materials-related aspects of the recent advances in microfluidics-based immunoassays for point-of-care (POC) diagnostics of biomarkers. We compare the materials for microfluidic chips fabrication in five aspects: fabrication, integration, function, modification and cost, and describe their advantages and drawbacks. In addition, we review materials for modifying antibodies to improve the performance of the reaction of immunoassay. We also review the state of the art in microfluidic immunoassays POC platforms, from the laboratory to routine clinical practice, and also commercial products in the market. Finally, we discuss the current challenges and future developments in microfluidic immunoassays. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Copper nanoparticle modified carbon electrode for determination of dopamine

    International Nuclear Information System (INIS)

    Oztekin, Yasemin; Tok, Mutahire; Bilici, Esra; Mikoliunaite, Lina; Yazicigil, Zafer; Ramanaviciene, Almira; Ramanavicius, Arunas

    2012-01-01

    This paper reports the synthesis and characterization of copper nanoparticles (CuNPs) and application of copper nanoparticle-modified glassy carbon electrode for the electrochemical determination of dopamine. Electrochemical measurements were performed using differently modified glassy carbon (GC) electrodes. Bare, oxidized before modification and copper nanoparticle-modified glassy carbon electrodes (bare-GC, ox-GC and CuNP/GC electrodes, respectively) were characterized by cyclic voltammetry and electrochemical impedance spectroscopy in the presence of redox probes. Atomic force microscopy was used for the visualization of electrode surfaces. The CuNP/GC electrode was found to be suitable for the selective determination of dopamine even in the presence of ascorbic acid, uric acid, and p-acetamidophenol. The observed linear range of CuNP/GC for dopamine was from 0.1 nM to 1.0 μM while the detection limit was estimated to be 50 pM. It was demonstrated that here reported glassy carbon electrode modified by copper nanoparticles is suitable for the determination of dopamine in real samples such as human blood serum.

  16. Fabrication and photocatalysis of mesoporous ZnWO4 with PAMAM as a template

    International Nuclear Information System (INIS)

    Lin Shen; Chen Jiebo; Weng Xiulan; Yang Liuyi; Chen Xinqin

    2009-01-01

    Mesoporous ZnWO 4 was prepared with the template of PAMAM. The as-formed samples were characterized by X-ray diffraction (XRD), nitrogen absorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-vis diffuse reflectance spectroscopy (DRS). It is found that the size of pore is in the range of 5-22 nm and that the porosity of ZnWO 4 is composed of aggregated ZnWO 4 nanoparticles. The photocatalytic activities towards degradation of rhodamine B (RhB) and malachite green (MG) under UV light has been investigated. The formation mechanism of mesoporous structures is proposed

  17. Luminescence and photothermally stimulated defects creation processes in PbWO4:La3+, Y3+ (PWO II) crystals

    International Nuclear Information System (INIS)

    Auffray, E.; Korjik, M.; Zazubovich, S.

    2015-01-01

    Photoluminescence and thermally stimulated luminescence (TSL) are studied for a PbWO 4 crystal grown by the Czochralski method at Bogoroditsk Technical Chemical Plant, Russia from the melt with a precise tuning of the stoichiometry and co-doped with La 3+ and Y 3+ ions (the PWO II crystal). Photothermally stimulated processes of electron and hole centers creation under selective UV irradiation of this crystal in the 3.5–5.0 eV energy range and the 85–205 K temperature range are clarified and the optically created electron and hole centers are identified. The electrons in PWO II are mainly trapped at the (WO 4 ) 2− groups located close to single La 3+ and Y 3+ ions, producing the electron {(WO 4 ) 3− –La 3+ } and {(WO 4 ) 3− –Y 3+ } centers. The holes are mainly trapped at the regular oxygen ions O 2− located close to La 3+ and Y 3+ ions associated with lead vacancies, producing the hole O − (I)-type centers. No evidence of single-vacancy-related centers has been observed in PWO II. The data obtained indicate that excellent scintillation characteristics of the PWO II crystal can be explained by a negligible concentration of single (non-compensated) oxygen and lead vacancies as the traps for electrons and holes, respectively. - Highlights: • Photoluminescence of the PbWO 4 :La 3+ , Y 3+ (PWO II) crystal is investigated. • Creation of defects under UV irradiation of PWO II is studied by TSL. • Origin of dominating electron and hole centers is ascertained. • Concentration of single-vacancy-related centers is found to be negligible. • Excellent scintillation characteristics of the PWO II crystal are explained.

  18. Hydrothermal deposition and photochromic performances of three kinds of hierarchical structure arrays of WO{sub 3} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Defang; Shen, Yi, E-mail: sysy7373@163.com; Ouyang, Yali; Li, Zhen

    2012-10-01

    Three kinds of tungsten oxide (WO{sub 3}) thin films have been fabricated by a simple hydrothermal deposition method. Scanning electron microscopy images of the products revealed that the capping agents did impact the microstructure of WO{sub 3} films. Films prepared without capping agents were ordered nanorod arrays, while the ones obtained with ethanol and oxalic acid revealed peeled-orange-like and cauliflower-like hierarchical structure arrays, respectively. Both of the two hierarchical structures were composed of much thinner nanorods compared with the one obtained without capping agents. All the WO{sub 3} films exhibited good photochromic properties and the two with inducers performed even better, which could be due to the changes in the microstructure that increased the amount of photogenerated electron-hole pairs and the proton diffusion rates. - Highlights: Black-Right-Pointing-Pointer Ordered WO{sub 3} nanorod arrays were prepared by hydrothermal deposition process. Black-Right-Pointing-Pointer Two hierarchical WO{sub 3} structure arrays were obtained with ethanol and oxalic acid. Black-Right-Pointing-Pointer Mechanism for the improved photochromic performances of WO{sub 3} films is proposed.

  19. Facile preparation of Z-scheme WO{sub 3}/g-C{sub 3}N{sub 4} composite photocatalyst with enhanced photocatalytic performance under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Lifeng, E-mail: lifeng.cui@gmail.com [School of Chemistry and Environmental Engineering, Dongguan University of Technology, Guangdong 523808 (China); Ding, Xiang; Wang, Yangang; Shi, Huancong; Huang, Lihua; Zuo, Yuanhui [Department of Environmental Science and Engineering, University of Shanghai for Science and Technology, Shanghai 200093 (China); Kang, Shifei, E-mail: sfkang@usst.edu.cn [Department of Environmental Science and Engineering, University of Shanghai for Science and Technology, Shanghai 200093 (China)

    2017-01-01

    Highlights: • WO{sub 3}/g-C{sub 3}N{sub 4} composites were synthesized through a facile mixing-and-heating method. • The composite showed improved visible light response. • The composite showed high activity for MB degradation. • Z-scheme charge carrier transfer pathways in the composite are proposed. - Abstract: Visible-light-driven WO{sub 3}/g-C{sub 3}N{sub 4} composites photocatalysts were synthesized via a facile one-step simultaneously heating procedure with urea as the main precursor. These prepared catalyst samples were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TG), transmission electron microscopy (TEM), N{sub 2} adsorption, ultraviolet-visible diffuse reflection spectroscopy (UV–vis), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) and electrochemical impedance spectroscopy (EIS). The photocatalytic activity of the WO{sub 3}/g-C{sub 3}N{sub 4} composites was evaluated by the photo-degradation of Rhodamine B (RhB) under visible light irradiation. The results indicated that the composites with 25 wt.% WO{sub 3} content exhibited highest photocatalytic activity compared to pure WO{sub 3}, bare g-C{sub 3}N{sub 4} and other WO{sub 3}/g-C{sub 3}N{sub 4} composites. The favorable photocatalytic activity of WO{sub 3}/g-C{sub 3}N{sub 4} composites was mainly attributed to the excellent surface properties, enhanced visible-light absorption and the desirable band positions. A possible Z-scheme photocatalytic mechanism was proposed based on structure and electrochemical characterizations results, which can well explain the enhanced migration rate of photogenerated electrons and holes in WO{sub 3}/g-C{sub 3}N{sub 4} heterojunctions.

  20. Role of indium tin oxide electrode on the microstructure of self-assembled WO3-BiVO4 hetero nanostructures

    Science.gov (United States)

    Song, Haili; Li, Chao; Van, Chien Nguyen; Dong, Wenxia; Qi, Ruijuan; Zhang, Yuanyuan; Huang, Rong; Chu, Ying-Hao; Duan, Chun-Gang

    2017-11-01

    Self-assembled WO3-BiVO4 nanostructured thin films were grown on a (001) yttrium stabilized zirconia (YSZ) substrate by the pulsed laser deposition method with and without the indium tin oxide (ITO) bottom electrode. Their microstructures including surface morphologies, crystalline phases, epitaxial relationships, interface structures, and composition distributions were investigated by scanning electron microscopy, high-resolution transmission electron microscopy, and X-ray energy dispersive spectroscopy. In both samples, WO3 formed nanopillars embedded into the monoclinic BiVO4 matrix with specific orientation relationships. In the sample with the ITO bottom electrode, an atomically sharp BiVO4/ITO interface was formed and the orthorhombic WO3 nanopillars were grown on a relaxed BiVO4 buffer layer with a mixed orthorhombic and hexagonal WO3 transition layer. In contrast, a thin amorphous layer appears at the interfaces between the thin film and the YSZ substrate in the sample without the ITO electrode. In addition, orthorhombic Bi2WO6 lamellar nanopillars were formed between WO3 and BiVO4 due to interdiffusion. Such a WO3-Bi2WO6-BiVO4 double heterojunction photoanode may promote the photo-generated charge separation and further improve the photoelectrochemical water splitting properties.

  1. Moessbauer effect study of hyperfine interaction of /sup 161/Dy and /sup 151/Eu in tungsten bronzes Dysub(0. 18) WO/sub 3/ and Eusub(0. 18) WO/sub 3/

    Energy Technology Data Exchange (ETDEWEB)

    Kisynska, K

    1979-01-01

    The Moessbauer technique was used to investigate the hyperfine interaction of /sup 161/Dy and /sup 151/Eu in cubic rare earth tungsten bronzes: Dysub(0.18)WO/sub 3/ and Eusub(0.18)WO/sub 3/. Well resolved hfs spectrum was obtained at 4.2 K for Dysub(0.18)WO/sub 3/. The effective hf field approximation sufficed to interpret the spectrum. The obtained hyperfine interaction parameters were: -g/sub 0/..beta..sub(N)Hsub(eff)=(805+-19) Mc/s and e/sup 2/qQ/sub 0//4 = (506+-56) Mc/s. These results imply that ground doublet of Dy/sup +3/ ion in bronze is a Kramers doublet Vertical Bar+-15/2> with asymmetrical hyperfine tensor Asub(z) non equal to 0, Asub(x) = Asub(y) = 0 and that local crystalline field at RE metal in tungsten bronze at 4.2 K cannot be cubic. From ME absorption spectra of Eusub(0.18)WO/sub 3/ taken at 4.2 K, 78 K and 300 K the values of quadrupole interaction constants for bronze lattice and its temperature dependence were obtained. These data indicate that a phase transition from the high temperature ideal perovskite structure to a distorted one occurs in RE bronzes and that the distortion concerns the nearest tungsten-oxygen environment of RE ion.

  2. Enhanced performance of direct Z-scheme CuS-WO 3 system towards photocatalytic decomposition of organic pollutants under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Song, Chundong; Wang, Xiang; Zhang, Jing; Chen, Xuebing; Li, Can

    2017-12-01

    CuS-WO3 composites were synthesized by an in situ solution method at low temperature. The crystalline phase, morphology, particle size, and the optical properties of CuS-WO3 samples were characterized by XRD, SEM, XPS, and UV–vis diffuse reflectance spectra. CuS-WO3 composites showed much higher activity for photocatalytic degradation of RhB as compared with WO3 and CuS. The degradation rate constant over 1 wt% CuS-WO3 catalyst was 4.4 times and 9.2 times higher than that of WO3 and CuS, respectively. It is found that holes (h+) and superoxide radical anions (O2-) are the dominant reactive species by using methanol, disodium ethylenediaminetetraacetate (EDTA) and ascorbic acid as scavengers. Band structure analysis shows that bottom of CB of WO3 is very similar with and higher (ca. 0.01 eV) than the top of VB of CuS. The results of PL showed that the similarity renders the recombination between photogenerated holes on the VB of CuS and photogenerated electrons on the CB of WO3 possible and easy, forming a direct Z-scheme in CuS-WO3. This result in that more electrons in the CB of CuS and holes in the VB of WO3 survived, and then participated in the photocatalytic degradation of RhB, showing an increased activity.

  3. Preparation of tungsten coatings on graphite by electro-deposition via Na2WO4–WO3 molten salt system

    International Nuclear Information System (INIS)

    Sun, Ning-bo; Zhang, Ying-chun; Jiang, Fan; Lang, Shao-ting; Xia, Min

    2014-01-01

    Highlights: • Tungsten coatings on graphite were firstly obtained by electro-deposition method via Na 2 WO 4 –WO 3 molten salt system. • Uniform and dense tungsten coatings could be easily prepared in each face of the sample, especially the complex components. • The obtained tungsten coatings are with high purity, ultra-low oxygen content (about 0.022 wt%). • Modulate pulse parameters can get tungsten coatings with different thickness and hardness. - Abstract: Tungsten coating on graphite substrate is one of the most promising candidate materials as the ITER plasma facing components. In this paper, tungsten coatings on graphite substrates were fabricated by electro-deposition from Na 2 WO 4 –WO 3 molten salt system at 1173 K in atmosphere. Tungsten coatings with no impurities were successfully deposited on graphite substrates under various pulsed current densities in an hour. By increasing the current density from 60 mA cm −2 to 120 mA cm −2 an increase of the average size of tungsten grains, the thickness and the hardness of tungsten coatings occurs. The average size of tungsten grains can reach 7.13 μm, the thickness of tungsten coating was in the range of 28.8–51 μm, and the hardness of coating was higher than 400 HV. No cracks or voids were observed between tungsten coating and graphite substrate. The oxygen content of tungsten coating is about 0.022 wt%

  4. Employment of modified Fe3 O4 nanoparticles using thermo-sensitive polymer for extraction and pre-concentration of cefexime in biological samples.

    Science.gov (United States)

    Naghibi, Saman; Sahebi, Hamed

    2018-02-01

    Cefexime is a useful antibiotic that can be prescribed to treat bacterial infections. Nanoparticles have been widely marketed as a universal solution among scientists. Many studies have been performed to modify nanoparticles to make them functional as extraction and pre-concentration agents and drug carriers. Temperature-sensitive polymers belong to a group of substances that undergo a major change in their physical features in response to temperature. Recently developed polymers can be used in many different areas, including modification of nanoparticles. In order to modify this nanoparticle, grafting copolymerization of Fe 3 O 4 nanoparticles was performed using poly (N-vinylcaprolactam) and 3-allyloxy-1,2-propanediol. The optimum conditions for pre-concentration of cefexime were studied. Under these optimum conditions, extraction recovery of biological samples in the range of 71-89% was obtained. The limit of detection and precision of proposed method were 4.5 × 10 -4  μg mL -1 and analysis of cefexime, in biological samples using the proposed method, the ability of this method to extract and pre-concentrate cefexime was confirmed. Also, satisfactory results from an in vitro study on drug release in simulated intestine media were obtained. Copyright © 2017 John Wiley & Sons, Ltd.

  5. Removal of reactive red-120 and 4-(2-pyridylazo) resorcinol from aqueous samples by Fe{sub 3}O{sub 4} magnetic nanoparticles using ionic liquid as modifier

    Energy Technology Data Exchange (ETDEWEB)

    Absalan, Ghodratollah, E-mail: gubsulun@yahoo.com [Professor Masoumi Laboratory, Department of Chemistry, College of Science, Shiraz University, Hafeziyeh, Fars, 71454 Shiraz (Iran, Islamic Republic of); Asadi, Mozaffar; Kamran, Sedigheh; Sheikhian, Leila [Professor Masoumi Laboratory, Department of Chemistry, College of Science, Shiraz University, Hafeziyeh, Fars, 71454 Shiraz (Iran, Islamic Republic of); Goltz, Douglas M. [Department of Chemistry, University of Winnipeg, Winnipeg, MB, R3B 2E9 Canada (Canada)

    2011-08-30

    Highlights: {yields} Ionic liquids modify the dye-adsorption characteristics of magnetic nanoparticles. {yields} Modified nanoparticles improved the sensitivity of dye measurements. {yields} Water-solubility is an important factor for choosing an ionic liquid as a modifier for nanoparticles. - Abstract: The nanoparticles of Fe{sub 3}O{sub 4} as well as the binary nanoparticles of ionic liquid and Fe{sub 3}O{sub 4} (IL-Fe{sub 3}O{sub 4}) were synthesized for removal of reactive red 120 (RR-120) and 4-(2-pyridylazo) resorcinol (PAR) as model azo dyes from aqueous solutions. The mean size and the surface morphology of the nanoparticles were characterized by TEM, DLS, XRD, FTIR and TGA techniques. Adsorption of RR-120 and PAR was studied in a batch reactor at different experimental conditions such as nanoparticle dosage, dye concentration, pH of the solution, ionic strength, and contact time. Experimental results indicated that the IL-Fe{sub 3}O{sub 4} nanoparticles had removed more than 98% of both dyes under the optimum operational conditions of a dosage of 60 mg, a pH of 2.5, and a contact time of 2 min when initial dyes concentrations of 10-200 mg L{sup -1} were used. The maximum adsorption capacity of IL-Fe{sub 3}O{sub 4} was 166.67 and 49.26 mg g{sup -1} for RR-120 and PAR, respectively. The isotherm experiments revealed that the Langmuir model attained better fits to the equilibrium data than the Freundlich model. The Langmuir adsorption constants were 5.99 and 3.62 L mg{sup -1} for adsorptions of RR-120 and PAR, respectively. Both adsorption processes were endothermic and dyes could be desorbed from IL-Fe{sub 3}O{sub 4} by using a mixed NaCl-acetone solution and adsorbent was reusable.

  6. Investigation of the La2O3-Nb2O5-WO3 ternary phase diagram: Isolation and crystal structure determination of the original La3NbWO10 material

    KAUST Repository

    Vu, T.D.

    2015-05-23

    In the course of the exploration of the La2O3-WO3-Nb2O5 ternary phase diagram, a new compound with the formula La3NbWO10 was discovered. Its structure was determined from a combination of powder X-ray and neutron diffraction data. It crystallizes in the tetragonal space group P42/nmc (no. 137) with the lattice parameters: a=10.0807(1) Å; c=12.5540(1) Å. The structure is built up from infinite ribbons of octahedra (W/Nb)O5 which are perpendicular to each other, lanthanum ions being distributed around these ribbons. The electrical properties of this compound were investigated on sintered pellets by means of complex impedance spectroscopy. © 2015 Elsevier Inc. All rights reserved.

  7. Evaluate humidity sensing properties of novel TiO{sub 2}–WO{sub 3} composite material

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Wang-De [Department of Applied Chemistry, Providence University, Taichung 43301 Taiwan, ROC (China); Department of Center for General Education, St. Mary' s Junior College of Medicine, Nursing and Management, Yilan 26644 Taiwan, ROC (China); Lai, De-Sheng; Chen, Min-Hung [Department of Applied Chemistry, Providence University, Taichung 43301 Taiwan, ROC (China); Wu, Ren-Jang, E-mail: rjwu@pu.edu.tw [Department of Applied Chemistry, Providence University, Taichung 43301 Taiwan, ROC (China); Chen, Fu-Chou [Department of Medical Research, Taichung Veterans General Hospital, Taichung 407, Taiwan, ROC (China)

    2013-10-15

    Graphical abstract: TiO{sub 2}–WO{sub 3} (1:1) showed better humidity sensing properties than others within the range of 12–90% relative humidity (RH), the response and recovery time were about 20 s and 160 s, respectively. Compared to the previous studies, the prepared sensor exhibits higher sensitivity (S = 451) and the low hysteresis value was around 0.13% at 32% RH. - Highlights: • Novel TiO{sub 2}–WO{sub 3} composite material was prepared for humidity sensor. • The sensor exhibits higher sensitivity (S = 451). • Low hysteresis value was around 0.13% at 32% RH. - Abstract: A novel TiO{sub 2}–WO{sub 3} composite material was prepared using a different proportion of TiO{sub 2} and WO{sub 3} to that investigated in previous studies. The obtained mesoporous material was characterized using X-ray diffraction, Fourier transform infrared spectrometry, transmission electron microscopy, energy dispersive X-ray spectroscopy, and N{sub 2} adsorption-desorption techniques. The humidity-sensing properties were measured using an inductance, capacitance and resistance analyzer. The results demonstrated that the TiO{sub 2}–WO{sub 3} sample with a ratio of 1:1 showed better humidity sensing properties. Compared to previous studies, the prepared sensor exhibited higher sensitivity (S = 451) and the lower hysteresis value was around 0.13% at 32% RH. Complex impedance analysis indicated that the enhanced humidity sensitivity was probably due to spherical Brunauer–Emmett–Teller surface area and the hetero-junction between TiO{sub 2}–WO{sub 3} thin films, while the impedance varied about three orders of magnitude. Our results demonstrated the potential application of TiO{sub 2}–WO{sub 3} composite for fabricating high performance humidity sensors.

  8. Er3+-Al2O3 nanoparticles doping of borosilicate glass

    International Nuclear Information System (INIS)

    Massera, Jonathan; Petit, Laeticia; Hupa, Leena; Hupa, Mikko; Koponen, Joona; Glorieux, Benoit

    2015-01-01

    Novel borosilicate glasses were developed by adding in the glass batch Er 3+ -Al 2 O 3 nanoparticles synthetized by using a soft chemical method. A similar nanoparticle doping with modified chemical vapour deposition (MCVD) process was developed to increase the efficiency of the amplifying silica fibre in comparison to using MCVD and solution doping. It was shown that with the melt quench technique, a Er 3+ -Al 2 O 3 nanoparticle doping neither leads to an increase in the Er 3+ luminescence properties nor allows one to control the rare-earth chemical environment in a borosilicate glass. The site of Er 3+ in the Er 3+ -Al 2 O 3 nanoparticle containing glass seems to be similar as in glasses with the same composition prepared using standard raw materials. We suspect the Er 3+ ions to diffuse from the nanoparticles into the glass matrix. There was no clear evidence of the presence of Al 2 O 3 nanoparticles in the glasses after melting. (author)

  9. Incorporation of polyoxotungstate complexes in silica spheres and in situ formation of tungsten trioxide nanoparticles.

    Science.gov (United States)

    Zhao, Yuanyuan; Fan, Haimei; Li, Wen; Bi, Lihua; Wang, Dejun; Wu, Lixin

    2010-09-21

    In this paper, we demonstrated a new convenient route for in situ fabrication of well separated small sized WO(3) nanoparticles in silica spheres, through a predeposition of surfactant encapsulated polyoxotungates as tungsten source, and followed by a calcination process. In a typical procedure, selected polyoxotungates with different charges were enwrapped with dioctadecyldimethylammonium cations through electrostatic interaction. Elemental analysis, thermogravimetric analysis, and spectral characterization confirmed the formation of prepared complexes with the anticipated chemical structure. The complexes were then phase-transferred into aqueous solution that predissolved surfactant cetyltrimethylammonium bromide, and finally incorporated into silica spheres through a joint sol-gel reaction with tetraethyl orthosilicate in a well dispersed state under the protection of organic layer for polyoxotungates from the alkaline reaction condition. Transmission electron microscopic images illustrated the well dispersed WO(3) nanoparticles in the size range of ca. 2.2 nm in the silica spheres after the calcination at 465 °C. The sizes of both the silica spheres and WO(3) nanoparticles could be adjusted independently through changing the doping content to a large extent. Meanwhile, the doped polyoxotungate complexes acted as the template for the mesoporous structure in silica spheres after the calcination. Along with the increase of doping content and surfactant, the mesopore size changed little (2.0-2.9 nm), but the specific surface areas increased quite a lot. Importantly, the WO(3)-nanoparticle-doped silica spheres displayed an interesting photovoltaic property, which is favorable for the funtionalization of these nanomaterials.

  10. Photocatalytic activity of titanium dioxide modified by Fe{sub 2}O{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Wodka, Dawid [J. Haber Institute of Catalysis and Surface Chemistry PAS, Niezapominajek 8, 30-239 Krakow (Poland); Department of Physical Chemistry, University of Geneva, 30 Quai Ernest-Ansermet, 1211 Geneva 4 (Switzerland); Socha, Robert P.; Bielańska, Elżbieta [J. Haber Institute of Catalysis and Surface Chemistry PAS, Niezapominajek 8, 30-239 Krakow (Poland); Elżbieciak-Wodka, Magdalena [J. Haber Institute of Catalysis and Surface Chemistry PAS, Niezapominajek 8, 30-239 Krakow (Poland); Department of Analytical Chemistry, University of Geneva, 30 Quai Ernest-Ansermet, 1211 Geneva 4 (Switzerland); Nowak, Paweł, E-mail: ncnowak@cyf-kr.edu.pl [J. Haber Institute of Catalysis and Surface Chemistry PAS, Niezapominajek 8, 30-239 Krakow (Poland); Warszyński, Piotr [J. Haber Institute of Catalysis and Surface Chemistry PAS, Niezapominajek 8, 30-239 Krakow (Poland)

    2014-11-15

    Highlights: • 1% Fe{sub 2}O{sub 3}/TiO{sub 2} composite showing high activity in the photocatalytic oxidation of organics was synthetized. • Electrochemical analysis indicated that surface modification of Degussa P25 by Fe{sub 2}O{sub 3} causes the appearance of surface states in such a material. • The enhanced activity of the prepared composite may be ascribed to the occurrence of the photo-Fenton process. - Abstract: Photocatalytic activity of Fe{sub 2}O{sub 3}/TiO{sub 2} composites obtained by precipitation was investigated. The composite material containing 1.0 wt% of iron(III) oxide nanoparticles was obtained by depositing Fe{sub 2}O{sub 3} on the Evonic-Degussa P25 titania surface. SEM, XPS, DRS, CV and EIS techniques were applied to examine synthetized pale orange photocatalyst. The XPS measurements revealed that iron is present mainly in the +3 oxidation state but iron in the +2 oxidation state can be also detected. Electrochemical analysis indicated that surface modification of Degussa P25 by Fe{sub 2}O{sub 3} causes the appearance of surface states in such a material. Nevertheless, based on the DRS measurement it was shown that iron(III) oxide nanoparticles modified the P25 spectral properties but they did not change the band gap width. The photocatalytic activity of Fe{sub 2}O{sub 3}/TiO{sub 2} composite was compared to photocatalytic activity of pristine P25 in photooxidation reaction of model compounds: oxalic acid (OxA) and formic acid (FA). Photodecomposition reaction was investigated in a batch reactor containing aqueous suspension of a photocatalyst illuminated by either UV or artificial sunlight (halogen lamp). The tests proved that nanoparticles deposited on titania surface triggers the increase in photocatalytic activity, this increase depends however on the decomposed substance.

  11. Photothermal ablation cancer therapy using homogeneous CsxWO3 nanorods with broad near-infra-red absorption

    Science.gov (United States)

    Guo, Chongshen; Yin, Shu; Yu, Haijun; Liu, Shaoqin; Dong, Qiang; Goto, Takehiro; Zhang, Zhiwen; Li, Yaping; Sato, Tsugio

    2013-06-01

    Recently, photothermal ablation therapy (PTA) employing near-infrared radiation (NIR) has been extensively investigated as an emerging modality for cancer management. However, the clinical translation of this promising approach is limited by the lack of PTA agents with broad NIR absorption, low cost and high photothermal conversion efficiency. Herein, we have developed PEGylated homogeneous CsxWO3 nanorods (a mean size ~69.3 nm × 12.8 nm) with broad photo-absorption (780-2500 nm) as a novel NIR absorbent for PTA treatment of human cancer. The prepared CsxWO3 nanocrystals displayed strong near-infrared optical absorption with a high molar extinction coefficient (e.g. 4.8 × 1010 M-1 cm-1 at 980 nm), thus generated significant amounts of heat upon excitation with near-infrared light. The PTA study in two human carcinoma cell lines (i.e. A549 lung cancer cells and HeLa ovarian cancer cells) demonstrated that CsxWO3 nanorods can efficiently cause cell death via hyperthermia induced lysosome destruction, cytoskeleton protein degradation, DNA damage and thereafter cellular necrosis or apoptosis. Our study also confirmed the migration of healthy cells migrated from unirradiated areas to dead cell cycle, which is essential for tissue reconstruction and wound healing after photodestruction of tumor tissue. The prompted results reported in the current study imply the promising potential of CsxWO3 nanorods for application in PTA cancer therapy.Recently, photothermal ablation therapy (PTA) employing near-infrared radiation (NIR) has been extensively investigated as an emerging modality for cancer management. However, the clinical translation of this promising approach is limited by the lack of PTA agents with broad NIR absorption, low cost and high photothermal conversion efficiency. Herein, we have developed PEGylated homogeneous CsxWO3 nanorods (a mean size ~69.3 nm × 12.8 nm) with broad photo-absorption (780-2500 nm) as a novel NIR absorbent for PTA treatment of human

  12. Effect of direct current density on microstructure of tungsten coating electroplated from Na{sub 2}WO{sub 4}-WO{sub 3}-NaPO{sub 3} system

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Fan, E-mail: jiangfan1109@163.com; Zhang, Yingchun, E-mail: zycustb@163.com; Sun, Ningbo, E-mail: suningbo682@163.com; Liu, Zhi’ang, E-mail: zhiang_001@163.com

    2014-10-30

    Highlights: • Tungsten coatings were electroplated from the Na{sub 2}WO{sub 4}-WO{sub 3}-NaPO{sub 3} melt. • Tungsten coating comprised a tooth-like layer and a columnar growth layer. • The average grain size increases as increasing current density. • (2 1 1) Orientation is favored most likely for samples obtained at various durations. • The growth rate of tungsten crystal nucleus is higher than the nucleation rate. - Abstract: Pure tungsten coating with body-centered cubic (bbc) structure was successfully electrodeposited from Na{sub 2}WO{sub 4}-WO{sub 3}-NaPO{sub 3} molten salt at 1153 K in atmosphere. The coatings comprised an inner layer of tooth-like grains and an outer layer of columnar grains with a thin diffusion layer of tungsten in the Cu substrate. The effects of current density and electrodeposition duration on the morphology and microstructure of the coatings were investigated in this paper. With increasing of current density from 50 to 80 mA cm{sup −2}, the grain size of the tungsten coating increased from 7.01 μm to 12.44 μm. With the increase of the current density, the thickness of the coating changed from 25.92 μm to 34.40 μm, and then dropped to 29.72 μm. The preferred orientation of the coatings changed from (2 2 0) to (2 1 1). With the increasing of duration, the grain size and thickness of tungsten coatings increased while the (2 1 1) favored orientation dot not changed. Because of the low current efficiency at long duration of direct current electrodeposition, it should not be suitable for the electroplating of thick tungsten coating.

  13. Structural studies of WO3-TeO2 glasses by high-Q-neutron diffraction and Raman spectroscopy

    International Nuclear Information System (INIS)

    Khanna, A.; Kaur, A.; Krishna, P.S.R.; Shinde, A.B.

    2013-01-01

    Glasses from the system: xWO 3 -(100-x)TeO 2 (x=15, 20 and 25 mol %) were prepared by melt quenching technique and characterized by density, UV-visible absorption spectroscopy, Differential Scanning Calorimetry (DSC), Raman spectroscopy and high-Q neutron diffraction measurements. Glass density and glass transition temperature increased with increase in WO 3 concentration, Raman spectroscopy indicated the conversion of TeO 4 units into TeO 3 units with increase in WO 3 content. The increase in glass transition temperature with the incorporation of WO 3 was attributed to the increase in average bond strength of the glass network since the bond dissociation energy of W-O bonds (672 kJ/mol) is significantly higher than that of Te-O bonds (376 kJ/mol). UV-visible studies found a very strong optical absorption band due to W 6+ ions, just below the absorption edge. High-Q neutron diffraction measurements were performed on glasses and radial distribution function analyses revealed changes in W-O and Te-O correlations in the glass network. The findings about changes in glass structure from neutron diffraction studies were consistent with structural information obtained from Raman spectroscopy and structure-property correlations were made. (author)

  14. Enhanced photocatalytic properties in well-ordered mesoporous WO3

    KAUST Repository

    Li, Li; Krissanasaeranee, Methira; Pattinson, Sebastian W.; Stefik, Morgan; Wiesner, Ulrich; Steiner, Ullrich; Eder, Dominik

    2010-01-01

    We used polyisoprene-block-ethyleneoxide copolymers as structure-directing agents to synthesise well-ordered and highly-crystalline mesoporous WO 3 architectures that possess improved photocatalytic properties due to enhanced dye-adsorption in absence of diffusion limitation. © 2010 The Royal Society of Chemistry.

  15. Electrochromism and local order in amorphous WO/sub 3/

    Energy Technology Data Exchange (ETDEWEB)

    Zeller, H R; Beyeler, H U

    1977-06-01

    WO/sub 3/ films prepared under different conditions (evaporation, reactive sputtering and spraying of aqueous solutions of metatungstic acid) differ by orders of magnitude in their electrochromic sensitivity. Diffuse X-ray studies show the evaporated and sputtered films to be amorphous and to consists of a disordered network of corner sharing WO/sub 6/ octahedra. Sprayed films have different degrees of crystallinity depending on spraying conditions. From differential scanning calorimetry we conclude that the crystal water present in most films strongly affects the local order of the corner sharing octahedra. We find that crystal water not only provides a high ionic conductivity which is conditional for a fast electrochromic reaction but also stabilises electrocatalytically active surface sites for fast hydrogen or Li exchange with the adjacent electrolyte.

  16. Luminescence properties of NaY(WO{sub 4}){sub 2}:Sm{sup 3+}, Eu{sup 3+} phosphors prepared by molten salt method

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Ting; Meng, Qingyu, E-mail: qingyumeng163@163.com; Sun, Wenjun

    2016-02-15

    Sm{sup 3+} singly doped NaY(WO{sub 4}){sub 2} and Sm{sup 3+}, Eu{sup 3+} co-doped NaY(WO{sub 4}){sub 2} phosphors have been synthesized by molten salt method. The crystal structure and morphology were characterized by means of X-ray powder diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). In Sm{sup 3+} singly doped NaY(WO{sub 4}){sub 2} phosphors, the suitable doping concentration was proved. In Sm{sup 3+}, Eu{sup 3+} co-doped NaY(WO{sub 4}){sub 2} phosphors, the energy transfer from Sm{sup 3+} to Eu{sup 3+} is confirmed by the luminescent spectra. A strong absorption line at 405 nm can be generated from {sup 6}H{sub 5/2}-{sup 4}K{sub 11/2} ({sup 4}F{sub 7/2}) transition of Sm{sup 3+} in Sm{sup 3+}, Eu{sup 3+} co-doped NaY(WO{sub 4}){sub 2} phosphors, which is suitable for the emission of the near-ultraviolet light-emitting diodes. The energy transfer efficiency, energy transfer rate and average distance between Sm{sup 3+} and Eu{sup 3+} in the NaY(WO{sub 4}){sub 2}:Sm{sup 3+}, Eu{sup 3+} phosphors have been calculated based on the fluorescent dynamic analysis. Finally, the energy transfer mechanism between Sm{sup 3+} and Eu{sup 3+} is confirmed, the energy transfer occurs between {sup 4}G{sub 5/2} state of Sm{sup 3+} ions and {sup 5}D{sub 0} state rather than {sup 5}D{sub 1} state of Eu{sup 3+} ions.

  17. Fluorometric immunoassay for human serum albumin based on its inhibitory effect on the immunoaggregation of quantum dots with silver nanoparticles

    Science.gov (United States)

    Marukhyan, Seda S.; Gasparyan, Vardan K.

    2017-02-01

    Quantitative determination of HSA was conducted by competitive immunoassay. Inhibition of aggregation of antibody conjugated quantum dots (QD) with albumin conjugated silver nanoparticles (AgNPs) in the presence of HSA was conducted. If antibody-loaded CdSe QDs aggregate with HSA-coated silver nanoparticles the distance between the two kinds of nanoparticles will be reduced enough to cause fluorescence resonance energy transfer (FRET). In this case the yellow fluorescence of the Ab-QDs is quenched. However if HSA (antigen) is added to the Ab-QDs their surface will be blocked and they cannot aggregate any longer with the HSA-AgNPs. Hence, fluorescence will not be quenched. The drop of the intensity of fluorescence (peaking at 570 nm) is inversely correlated with the concentration of HSA in the sample. The method allows to determine HSA in the 30-600 ng·mL-1 concentration range.

  18. Cerium oxide-deposited mesoporous silica nanoparticles for the determination of carcinoembryonic antigen in serum using inductively coupled plasma-mass spectrometry

    International Nuclear Information System (INIS)

    Choi, H.W.; Lee, K.H.; Hur, N.H.; Lim, H.B.

    2014-01-01

    Highlights: • Sandwich-type immunoassay using ICP-MS and nanoparticles to determine biomarkers. • CeO 2 -deposited mesoporous silica nanoparticles were synthesized as a probe. • Ratiometric measurement significantly improved the calibration linearity. • Excellent detection limit was achieved by signal amplification. - Abstract: CeO 2 -deposited mesoporous silica nanoparticles were synthesized as a probe to determine carcinoembryonic antigen (CEA) in serum by inductively coupled plasma-mass spectrometry (ICP-MS). The prepared mesoporous nanoparticles were modified and tagged to the target for sandwich-type immunoassay. Fe 3 O 4 magnetic nanoparticles (MNPs) were also synthesized and immobilized with antibody to extract the target biomarker. The calibration curve of the synthesized CeO 2 -deposited silica nanoparticles, which was plotted by the signal ratio of 140 Ce/ 57 Fe measured by ICP-MS vs. the concentration of CEA, showed excellent linearity and sensitivity owing to the signal amplification and low spectral interference. Under optimal conditions, the sandwich-type analytical method was applied to determine CEA in serum spiked in the range of 0.001–5 ng mL −1 and showed a limit of detection of 0.36 ng mL −1 . Since the deposited CeO 2 in the mesoporous silica layer can be substituted by other metal compounds, various kinds of metal-deposited nanoparticles can be prepared as probe materials for multiplex detection in bioanalysis

  19. Magnetofluorescent nanocomposites and quantum dots used for optimal application in magnetic fluorescence-linked immunoassay.

    Science.gov (United States)

    Tsai, H Y; Li, S Y; Fuh, C Bor

    2018-03-01

    Magnetofluorescent nanocomposites with optimal magnetic and fluorescent properties were prepared and characterized by combining magnetic nanoparticles (iron oxide@polymethyl methacrylate) with fluorescent nanoparticles (rhodamine 6G@mSiO 2 ). Experimental parameters were optimized to produce nanocomposites with high magnetic susceptibility and fluorescence intensity. The detection of a model biomarker (alpha-fetoprotein) was used to demonstrate the feasibility of applying the magnetofluorescent nanocomposites combined with quantum dots and using magnetic fluorescence-linked immunoassay. The magnetofluorescent nanocomposites enable efficient mixing, fast re-concentration, and nanoparticle quantization for optimal reactions. Biofunctional quantum dots were used to confirm the alpha-fetoprotein (AFP) content in sandwich immunoassay after mixing and washing. The analysis time was only one third that required in ELISA. The detection limit was 0.2 pg mL -1 , and the linear range was 0.68 pg mL -1 -6.8 ng mL -1 . This detection limit is lower, and the linear range is wider than those of ELISA and other methods. The measurements made using the proposed method differed by less than 13% from those obtained using ELISA for four AFP concentrations (0.03, 0.15, 0.75, and 3.75 ng mL -1 ). The proposed method has a considerable potential for biomarker detection in various analytical and biomedical applications. Graphical abstract Magnetofluorescent nanocomposites combined with fluorescent quantum dots were used in magnetic fluorescence-linked immunoassay.

  20. Gold nanoparticles modified with coordination compounds of metals: synthesis and application

    International Nuclear Information System (INIS)

    Beloglazkina, Elena K; Majouga, Alexander G; Romashkina, Renata B; Zyk, Nikolai V; Zefirov, Nikolai S

    2012-01-01

    The data on the preparation methods and applications of gold nanoparticles with coordinated metal ions on the surfaces are generalized. The currently available data on the interaction of metal ions with gold nanoparticles modified with organic (particularly, sulfur-containing) ligands comprising terminal chelating groups are considered in detail as well as the applications of such modified nanoparticles. The bibliography includes 141 references.

  1. Modification of the performance of WO{sub 3}-ZrO{sub 2} catalysts by metal addition in hydrocarbon reactions

    Energy Technology Data Exchange (ETDEWEB)

    Torres, Gerardo Carlos; Manuale, Debora Laura; Benitez, Viviana Monica; Vera, Carlos Roman; Yori, Juan Carlos, E-mail: jyori@fiq.unl.edu.ar [Instituto de Investigaciones en Catalisis y Petroquimica, Facultad de Ingenieria Quimica, Universidad Nacional del Litoral, Consejo Nacional de Investigaciones Cientifica y Tecnicas, Santiago del Estero Santa Fe (Argentina)

    2012-07-01

    A study of the different hydrocarbon reactions over Ni doped WO{sub 3}-ZrO{sub 2} catalysts was performed. Ni was found as NiO at low Ni concentration while at high Ni concentrations a small fraction was present as a metal. For both cases, Ni strongly modified total acidity and concentration of strong acid sites. In the cyclohexane dehydrogenation reaction, Ni addition promotes both benzene and methyl cyclopentane production. The hydroconversion activity (n-butane and n-octane) increases with the augment of total acidity produced by Ni. The selectivity to reaction products is modified according to the acid strength distribution changes produced by Ni addition. (author)

  2. Gum arabic modified Fe3O4 nanoparticles cross linked with collagen for isolation of bacteria

    Directory of Open Access Journals (Sweden)

    Chittor Raghuraman

    2010-12-01

    Full Text Available Abstract Background Multifunctional magnetic nanoparticles are important class of materials in the field of nanobiotechnology, as it is an emerging area of research for material science and molecular biology researchers. One of the various methods to obtain multifunctional nanomaterials, molecular functionalization by attaching organic functional groups to nanomagnetic materials is an important technique. Recently, functionalized magnetic nanoparticles have been demonstrated to be useful in isolation/detection of dangerous pathogens (bacteria/viruses for human life. Iron (Fe based material especially FePt is used in the isolation of ultralow concentrations (2 cfu/ml of bacteria in less time and it has been demonstrated that van-FePt may be used as an alternative fast detection technique with respect to conventional polymerase chain reaction (PCR method. However, still further improved demonstrations are necessary with interest to biocompatibility and green chemistry. Herein, we report the synthesis of Fe3O4 nanoparticles by template medication and its application for the detection/isolation of S. aureus bacteria. Results The reduction of anhydrous Iron chloride (FeCl3 in presence of sodium borohydride and water soluble polyelectrolyte (polydiallyldimethyl ammonium chloride, PDADMAC produces black precipitates. The X-ray diffraction (XRD, XPS and TEM analysis of the precipitates dried at 373 K demonstrated the formation of nanocrystalline Fe3O4. Moreover, scanning electron microscopy (SEM showed isolated staphylococcous aureus (S. aureus bacteria at ultralow concentrations using collagen coated gum arabic modified iron oxide nanoparticles (CCGAMION. Conclusion We are able to synthesize nanocrystalline Fe3O4 and CCGAMION was able to isolate S. aureus bacteria at 8-10 cfu (colony forming units/ml within ~3 minutes.

  3. A comparative study of humidity sensing and photocatalytic applications of pure and nickel (Ni)-doped WO{sub 3} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Ramkumar, S. [Bannari Amman Institute of Technology, Department of Physics, Erode, Tamilnadu (India); Rajarajan, G. [Vidhya Mandhir Institute of Technology, Department of Physics, Erode, Tamilnadu (India)

    2017-06-15

    Nanocrystalline of pristine and nickel (Ni)-doped tungsten trioxide (WO{sub 3}) thin films was deposited by chemical bath deposition method. The concentrations of Ni ions were varied from 0 to 10 wt%. In order to improve the crystallinity of the films were annealed at 600 C for 2 h in the ambient atmosphere. X-ray diffraction results reveal that the WO{sub 3} doped with nickel crystallizes in monoclinic structure and the results are in good agreement with the standard JCPDS data (card no: 83-0951). AFM micrographs reveal that average grain size of about 27-39 nm for pure and Ni-doped WO{sub 3} thin films. In addition, the band gap of the Ni-doped WO{sub 3} nanostructures is facilely tunable by controlling the Ni contents. The humidity sensor setup was fabricated and measured for pure and Ni-doped WO{sub 3} thin film sensor with various level of RH (10-90%). The Ni-doped WO{sub 3} sensor showed fast response and high sensitivity than pure WO{sub 3}. The photocatalytic activities of the films were evaluated by degradation of methyl orange, methylene blue and phenol in an aqueous solution under visible light irradiation. The photocatalytic activity of WO{sub 3} nanostructures could be remarkably enhanced by doping the Ni impurity. (orig.)

  4. Chemical sensors based on molecularly modified metallic nanoparticles

    International Nuclear Information System (INIS)

    Haick, Hossam

    2007-01-01

    This paper presents a concise, although admittedly non-exhaustive, didactic review of some of the main concepts and approaches related to the use of molecularly modified metal nanoparticles in or as chemical sensors. This paper attempts to pull together different views and terminologies used in sensors based on molecularly modified metal nanoparticles, including those established upon electrochemical, optical, surface Plasmon resonance, piezoelectric and electrical transduction approaches. Finally, this paper discusses briefly the main advantages and disadvantages of each of the presented class of sensors. (review article)

  5. Antimicrobial effects of zinc oxide nanoparticles modified with silver

    International Nuclear Information System (INIS)

    Lopes, Rayssa Souza; Arantes, Tatiane Moraes

    2016-01-01

    Full text: With the emergence of resistant microbial organisms to multiple antibiotics, different shapes of silver nanoparticles are among the most promising antimicrobial agents that have been developed from nanotechnology. Besides the silver nanoparticles oxide nanoparticles such as zinc oxide (ZnO) is gaining prominence due to its bactericidal properties. [1-3]. Thus, this study aims to develop biomaterials from zinc oxide nanoparticles modified with silver with antimicrobial properties. The ZnO nanoparticles were synthesized by hydrothermal processing by alkaline hydrolysis zinc acetate. Colloidal dispersions of silver nanoparticles were synthesized by the Turkevich method using sodium citrate to reduce silver nitrate at high pH and at 90 °C in the presence of zinc oxide nanoparticles. Both nanoparticles were characterized by X-ray diffraction (XRD), FTIR and Raman spectroscopy and scanning electron microscopy (SEM). The XRD and Raman spectra showed crystalline ZnO colloidal nanoparticles were obtained in the hexagonal phase. XRD measure showed cubic silver diffraction peaks cubic phase confirmed the presence of the silver nanoparticles decorated zinc oxide nanoparticles. SEM images showed ZnO nanoparticles presented a nanorod shapes with length around 80 nm decorated with spherical silver nanoparticles about 20 nm in diameter The results showed that crystalline zinc oxide colloidal nanoparticles with rod-like morphology and uniform decorated with silver spherical nanoparticles size were obtained by hydrothermal synthesis. Results of antibacterial tests indicate that the ZnO/Ag nanoparticles have antibacterial properties against both Staphylococcus aureus and Escherichia coli. The results demonstrated that the ZnO/Ag nanoparticles have potential use as biomaterials in medical/odontological applications. (author)

  6. Antimicrobial effects of zinc oxide nanoparticles modified with silver

    Energy Technology Data Exchange (ETDEWEB)

    Lopes, Rayssa Souza; Arantes, Tatiane Moraes, E-mail: rayssasouza.net@gmail.com [Universidade Federal de Goias (UFG), Goiania (Brazil)

    2016-07-01

    Full text: With the emergence of resistant microbial organisms to multiple antibiotics, different shapes of silver nanoparticles are among the most promising antimicrobial agents that have been developed from nanotechnology. Besides the silver nanoparticles oxide nanoparticles such as zinc oxide (ZnO) is gaining prominence due to its bactericidal properties. [1-3]. Thus, this study aims to develop biomaterials from zinc oxide nanoparticles modified with silver with antimicrobial properties. The ZnO nanoparticles were synthesized by hydrothermal processing by alkaline hydrolysis zinc acetate. Colloidal dispersions of silver nanoparticles were synthesized by the Turkevich method using sodium citrate to reduce silver nitrate at high pH and at 90 °C in the presence of zinc oxide nanoparticles. Both nanoparticles were characterized by X-ray diffraction (XRD), FTIR and Raman spectroscopy and scanning electron microscopy (SEM). The XRD and Raman spectra showed crystalline ZnO colloidal nanoparticles were obtained in the hexagonal phase. XRD measure showed cubic silver diffraction peaks cubic phase confirmed the presence of the silver nanoparticles decorated zinc oxide nanoparticles. SEM images showed ZnO nanoparticles presented a nanorod shapes with length around 80 nm decorated with spherical silver nanoparticles about 20 nm in diameter The results showed that crystalline zinc oxide colloidal nanoparticles with rod-like morphology and uniform decorated with silver spherical nanoparticles size were obtained by hydrothermal synthesis. Results of antibacterial tests indicate that the ZnO/Ag nanoparticles have antibacterial properties against both Staphylococcus aureus and Escherichia coli. The results demonstrated that the ZnO/Ag nanoparticles have potential use as biomaterials in medical/odontological applications. (author)

  7. Synthesis and characterization of large WO{sub 3} sheets synthesized by resistive heating method

    Energy Technology Data Exchange (ETDEWEB)

    Filippo, Emanuela, E-mail: emanuela.filippo@unisalento.it [Department of Engineering for Innovation, University of Salento, Monteroni Street, Lecce I-73100 Italy (Italy); Tepore, Marco [Department of Engineering for Innovation, University of Salento, Monteroni Street, Lecce I-73100 Italy (Italy); Baldassarre, Francesca [Department of Cultural Heritage, University of Salento, Lecce I-73100 Italy (Italy); Quarta, Gianluca; Calcagnile, Lucio [Department of Engineering for Innovation, University of Salento, Monteroni Street, Lecce I-73100 Italy (Italy); Guascito, Maria Rachele [DiSTeBA, University of Salento, Lecce I-73100 Italy (Italy); Tepore, Antonio [Department of Cultural Heritage, University of Salento, Lecce I-73100 Italy (Italy)

    2015-09-01

    A simple, low-cost method is presented to grow tungsten oxide large sheets simply by resistively heating a pure tungsten filament under air/water vapor flow. The obtained structures were studied using scanning and transmission electron microscopy, selected area diffraction, X Ray diffraction, Raman and X-ray photoelectron spectroscopy, photoluminescence and zeta potential measurements. SEM observations revealed that sheets formed by broadening of the wires/belts over longer growth period. Photoluminescence measurements showed that tungsten oxide sheets had an intense visible emission band. - Highlights: • WO{sub 3} large sheets were prepared by resistively heating a W filament. • WO{sub 3} sheets were carefully characterized. • Formation mechanism of sheets was studied. • WO{sub 3} sheets had an intense visible emission band at 462 nm.

  8. Polarized spectroscopic properties of Nd3+-doped KGd(WO4)2 single crystal

    International Nuclear Information System (INIS)

    Chen Yujin; Lin Yanfu; Gong Xinghong; Tan Qiguang; Zhuang Jian; Luo Zundu; Huang Yidong

    2007-01-01

    The polarized absorption spectra, infrared fluorescence spectra, upconversion visible fluorescence spectra, and fluorescence decay curve of orientated Nd 3+ :KGd(WO 4 ) 2 crystal were measured at room-temperature. Some important spectroscopic parameters were investigated in detail in the framework of the Judd-Ofelt theory and the Fuchtbauer-Ladenburg formula. The effect of the crystal structure on the spectroscopic properties of the Nd 3+ ions was analyzed. The relation among the spectroscopic parameters and the laser performances of the Nd 3+ :KGd(WO 4 ) 2 crystal was discussed

  9. Dipodal Silane-modified Nano Fe3O4/Polyurethane Magnetic Nanocomposites: Preparation and Characterization

    Directory of Open Access Journals (Sweden)

    Mir Mohammad Alavi Nikje

    2016-01-01

    Full Text Available Magnetic nanocomposites were prepared by incorporation of pure Fe3O4 and surface-modified Fe3O4 nanoparticles (dipodal silane-modified Fe3O4 into a polyurethane elastomer matrix by in situ polymerization method. In preparation of these magnetic nanocomposites, polycaprolactone (PCL was used as a polyester polyol. Because of dipole-dipole interactions between nanoparticles and a large surface area to volume ratio, the magnetic iron oxide nanoparticles tended to agglomerate. Furthermore, the most important challenge was to coat the surface of magnetic Fe3O4 nanoparticles in order to prepare well dispersed and stabilized Fe3O4 magnetic nanoparticles. It was observed that surface modification of Fe3O4 nanoparticles enhanced the dispersion of the nanoparticles in polyurethane matrices and allowed magnetic nanocomposites to be prepared with better properties. Surface modification of Fe3O4 was performed by dipodal silane synthesized based on 3-aminopropyltriethoxysilane (APTS and γ-glycidoxypropyl trimethoxysilane (GPTS. Dipodal silane-coated magnetic nanoparticles (DScMNPs were synthesized and incorporated into the polyurethane elastomer matrix as reinforcing agents. The formation of dipodal silane was investigated by Fourier transform infrared spectroscopy (FTIR, proton nuclear magnetic resonance spectroscopy (1H NMR and transmission electron microscopy (TEM. Characterization and study on the magnetic polyurethane elastomer nanocomposites were performed by FTIR, thermogravimetric analysis (TGA, scanning electron microscopy (SEM, vibrating sample magnetometry (VSM and dynamic mechanical thermal analysis (DMTA. The VSM results showed that the synthesized polyurethane elastomer nanocomposites had a superparamagnetic behavior. The TGA results showed that the thermal stability of dipodal silane-modified Fe3O4/PU nanocomposite was higher than that of Fe3O4/PU nanocomposite. This could be attributed to better dispersion and compatibility of dipodal silane-modified

  10. Modified surface of titanium dioxide nanoparticles-based biosensor for DNA detection

    Science.gov (United States)

    Nadzirah, Sh.; Hashim, U.; Rusop, M.

    2018-05-01

    A new technique was used to develop a simple and selective picoammeter DNA biosensor for identification of E. coli O157:H7. This biosensor was fabricated from titanium dioxide nanoparticles that was synthesized by sol-gel method and spin-coated on silicon dioxide substrate via spinner. 3-Aminopropyl triethoxy silane (APTES) was used to modify the surface of TiO2. Simple surface modification approach has been applied; which is single dropping of APTES onto the TiO2 nanoparticles surface. Carboxyl modified probe DNA has been bind onto the surface of APTES/TiO2 without any amplifier element. Electrical signal has been used as the indicator to differentiate each step (surface modification of TiO2 and probe DNA immobilization). The I-V measurements indicate extremely low current (pico-ampere) flow through the device which is 2.8138E-10 A for pure TiO2 nanoparticles, 2.8124E-10 A after APTES modification and 3.5949E-10 A after probe DNA immobilization.

  11. Multifunctionality in coating films including Nb-doped TiO2 and Cs x WO3: near infrared shielding and photocatalytic properties

    Science.gov (United States)

    Asakura, Yusuke; Anada, Yuto; Hamanaka, Ryo; Sato, Tsugio; Katsumata, Ken-ichi; Wu, Xiaoyong; Yin, Shu

    2018-06-01

    Various types of coating films were obtained from hydrothermally synthesized Nb-doped TiO2 (NTO) and Cs x WO3 (CWO) nanoparticles. The coating films possessed multifunctionality including near infrared (NIR) absorption and photocatalysis abilities. The NTO and CWO nanoparticles were synthesized by a unique solvothermal reaction in which water induced by an esterification reaction between alcohol and carboxylic acid can act as a hydrolyzing agent for metal precursors. NTO was synthesized by the unique solvothermal reaction for the first time. The reaction accompanied by the reduction of Ti4+ to Ti3+ led to the formation of nanoparticles with both NIR absorption and photocatalytic properties. The effect of the ethanol–acetic acid ratio on the morphology of the obtained NTO was investigated, and the larger amount of acetic acid led to a larger nanoparticle size, indicating the size controllability. The two types of coating film, including CWO and NTO nanoparticles, were obtained for comparison: (1) coexistent coating film: one side of the quartz glass was coated with a dispersion, including both CWO and NTO nanoparticles, and (2) double-sided coating film: a quartz glass coated with a CWO dispersion on one side and an NTO dispersion on the other side. The double-sided coating led to higher multifunctionality. Furthermore, the optimized condition for the double-sided coating was investigated by using various NTO particles obtained using different ethanol–acetic acid ratios.

  12. Photoluminescence characteristics of Sm{sup 3+}-doped Ba{sub 2}CaWO{sub 6} as new orange–red emitting phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Ruiijn [College of Science, Northwest A and F University, Yangling, Shaanxi 712100 (China); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Mi Noh, Hyeon; Kee Moon, Byung; Chun Choi, Byung [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Hyun Jeong, Jung, E-mail: jhjeong@pknu.ac.kr [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Sueb Lee, Ho [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Soo Yi, Soung [Department of Electronic Material Engineering, Silla University, Busan 617-736 (Korea, Republic of)

    2014-08-01

    The orange–red emitting Ba{sub 2}CaWO{sub 6}:xSm{sup 3+} (0.01≤x≤0.25) phosphors were synthesized via solid state reaction process. The crystal structure of the phosphor was characterized by XRD. The photoluminescence excitation and emission spectra, concentration effect were investigated. The results show an efficient energy transfer from WO{sub 6}{sup 6−} group to Sm{sup 3+} occurs. The emission spectra of the Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} phosphors consisted of some sharp emission peaks of Sm{sup 3+} ions centre at 579 nm, 618 nm, 625 nm, and 675 nm. The strongest one is located at 610 nm due to {sup 4}G{sub 5/2}→{sup 6}H{sub 7/2} transition of Sm{sup 3+}, generating bright orange–red light. The optimum dopant concentration of Sm{sup 3+} ions in Ba{sub 2}CaWO{sub 6}:xSm{sup 3+} is around 5 mol% and the critical transfer distance of Sm{sup 3+} is calculated as 18 Å. The fluorescence lifetime of Sm{sup 3+} in Ba{sub 2}CaWO{sub 6}:0.05Sm{sup 3+} is 2.36 ms. The Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} phosphors may be potentially used as orange–red phosphors for white light-emitting diodes. - Highlights: • A new host-sensitized Sm{sup 3+}-doped Ba{sub 2}CaWO{sub 6} phosphor was firstly synthesized. • Its structure, luminescent properties are well studied and characterized. • There exists an efficient energy transfer from WO{sub 6}{sup 6−} group to Sm{sup 3+}. • The thermal quenching properties of Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} was firstly evaluated.

  13. Preparation and photoelectric properties of p-CaFe{sub 2}O{sub 4}/n-WO{sub 3} composites

    Energy Technology Data Exchange (ETDEWEB)

    Wan, Ruiqin; Jia, Caihong [Key Laboratory of Photovoltaic Materials of Henan Province and School of Physics and Electronics, Henan University, Kaifeng 475004 (China); Zhang, Weifeng, E-mail: wfzhang@henu.edu.cn [Key Laboratory of Photovoltaic Materials of Henan Province and School of Physics and Electronics, Henan University, Kaifeng 475004 (China)

    2012-12-15

    Highlights: Black-Right-Pointing-Pointer Surface photovoltage spectroscopy investigation on p-CaFe{sub 2}O{sub 4}/n-WO{sub 3} composites. Black-Right-Pointing-Pointer The photovoltaic response is enhanced in p-CaFe{sub 2}O{sub 4}/n-WO{sub 3} composites. Black-Right-Pointing-Pointer The multielectron process and high rate of carrier migration in WO{sub 3}. - Abstract: Composites of p-CaFe{sub 2}O{sub 4}/n-WO{sub 3} are prepared via a sol-gel technique. Their structures and optical properties are characterized with X-ray diffraction, scanning electron microscopy and UV-vis absorption spectroscopy. The photoelectric characteristics are investigated by surface photovoltage spectroscopy combined with electric field induced surface photovoltage spectroscopy. The results indicate that CaFe{sub 2}O{sub 4} can well form a p-n type composite with WO{sub 3}, and the intensity and spectral region of surface photovoltaic response for the composites are strongly dependent on the molar ratio of two components. The enhancement in photoelectric properties and the effective separation of photogenerated carriers could be attributed to the energy level matching between the two components, multielectron process and the high migration rate in WO{sub 3}.

  14. Negative thermal expansion in Sc2(WO4)3

    International Nuclear Information System (INIS)

    Evans, J.S.O.; Mary, T.A.; Sleight, A.W.

    1998-01-01

    Sc 2 (WO 4 ) 3 has been found to show the highly unusual property of negative thermal expansion over a temperature range of 10 to 1,073 K. Powder neutron diffraction data from 10 to 450 K shows an essentially linear decrease in cell volume as a function of temperature. The intrinsic linear coefficient of thermal expansion from this data is -2.2 x 10 -6 K -1 . The linear coefficient of thermal expansion measured on a ceramic bar of Sc 2 (WO 4 ) 3 can be as negative as -11 x 10 -6 K -1 due to microstructure changes as a function of temperature. Rietveld refinement as a function of temperature suggests that the intrinsic negative thermal expansion can be related to transverse vibrations of bridging oxygen atoms in the structure. The anharmonic nature of these vibrations leads to a coupled tilting of the quasi-rigid framework polyhedra. This tilting in turn causes the structure to become more dense with increasing temperature

  15. Exfoliated thin Bi{sub 2}MoO{sub 6} nanosheets supported on WO{sub 3} electrode for enhanced photoelectrochemical water splitting

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Ying; Jia, Yulong; Wang, Lina [State Key Laboratory for Oxo Synthesis & Selective Oxidation, and National Engineering Research Center for Fine Petrochemical Intermediates, Lanzhou Institute of Chemical Physics, CAS, Lanzhou 730000 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Yang, Min [State Key Laboratory for Oxo Synthesis & Selective Oxidation, and National Engineering Research Center for Fine Petrochemical Intermediates, Lanzhou Institute of Chemical Physics, CAS, Lanzhou 730000 (China); Bi, Yingpu, E-mail: yingpubi@licp.cas.cn [State Key Laboratory for Oxo Synthesis & Selective Oxidation, and National Engineering Research Center for Fine Petrochemical Intermediates, Lanzhou Institute of Chemical Physics, CAS, Lanzhou 730000 (China); Qi, Yanxing, E-mail: qiyx@licp.cas.cn [State Key Laboratory for Oxo Synthesis & Selective Oxidation, and National Engineering Research Center for Fine Petrochemical Intermediates, Lanzhou Institute of Chemical Physics, CAS, Lanzhou 730000 (China)

    2016-12-30

    Highlights: • Thin Bi{sub 2}MoO{sub 6} nanosheets were prepared by microwave assisted ultrasonic separation. • The thin Bi{sub 2}MoO{sub 6} nanosheets could be more favorable to charge shift and separation. • The WO{sub 3}/thin Bi{sub 2}MoO{sub 6} exhibits superior photoelectric activity than WO{sub 3}/Bi{sub 2}MoO{sub 6} film. • The efficient photoelectric property results from facilitated charge separation. - Abstract: Thin Bi{sub 2}MoO{sub 6} nanosheets are obtained by a microwave-assisted ultrasonic separation process. After exfoliation, the thinner and uniform nanosheets with a thickness of about 10 nm were obtained. The exfoliated nanosheets would provide many amazing functionalities such as high electron mobility and quantum Hall effects. Therefore, thin Bi{sub 2}MoO{sub 6} supported on WO{sub 3} electrode (WO{sub 3}/thin Bi{sub 2}MoO{sub 6}) exhibits facilitated charge separation than pure WO{sub 3} film and the un-exfoliated Bi{sub 2}MoO{sub 6} nanosheets supported on WO{sub 3} electrode (WO{sub 3}/Bi{sub 2}MoO{sub 6}). As a result, WO{sub 3}/thin Bi{sub 2}MoO{sub 6} shows remarkably stable photocurrent density of 2.2 mA/cm{sup 2} at 0.8 V{sub SCE} in 0.1 M Na{sub 2}SO{sub 4} which is higher than that of that of WO{sub 3} (1.1 mA/cm{sup 2}) and WO{sub 3}/Bi{sub 2}MoO{sub 6} (1.5 mA/cm{sup 2}).

  16. A mesoporous WO3−X/graphene composite as a high-performance Li-ion battery anode

    International Nuclear Information System (INIS)

    Liu, Fei; Kim, Jong Gu; Lee, Chul Wee; Im, Ji Sun

    2014-01-01

    Graphical abstract: The highly flexible and conductive graphene layer can enhance electron transfer, protect metal oxides against disintegration and aggregation and buffer the strain induced by volume expansion during cycles. The mesoporous surface layer provides an open network for Li+ diffusion. - Highlights: • Novel cocktail effects of 2D mesoporous WO 3−X /graphene for lithium ion battery. • New approach for lithium ion battery by easy and unique synthesis method. • Mechanism study with proper data for understanding a reaction on anode surface. - Abstract: A novel mesoporous WO 3−X /graphene composite was developed. This material allowed rapid electron and Li + ion diffusion when used as a Li-ion battery (LIB) anode material. Remarkably, the graphene support protected WO 3−X from changing volume during the electrochemical cycling process; this process generally induces capacity loss. The current work describes a high-performance anode material for LIB that has highly dense WO 3−X , as well as high capacity, rate capability and stability

  17. Adsorption of environmental pollutants using magnetic hybrid nanoparticles modified with β-cyclodextrin

    International Nuclear Information System (INIS)

    Wang, Niejun; Zhou, Lilin; Guo, Jun; Ye, Qiquan; Lin, Jin-Ming; Yuan, Jinying

    2014-01-01

    Graft through strategy was utilized to coat magnetic Fe 3 O 4 nanoparticles with poly(glycidyl methacrylate) using ordinary radical polymerization and then β-cyclodextrin was linked onto the surface of nanoparticles. With these nanoparticles modified with cyclodextrin groups, adsorption of two model environmental pollutants, bisphenol A and copper ions, was studied. Host–guest interactions between cyclodextrin and aromatic molecules had a great contribution to the adsorption of bisphenol A, while multiple hydroxyls of cyclodextrin also helped the adsorption of copper ions. These magnetic nanoparticles could be applied in the elimination, enrichment and detection of some environmental pollutants.

  18. Morphology and structural studies of WO_3 films deposited on SrTiO_3 by pulsed laser deposition

    International Nuclear Information System (INIS)

    Kalhori, Hossein; Porter, Stephen B.; Esmaeily, Amir Sajjad; Coey, Michael; Ranjbar, Mehdi; Salamati, Hadi

    2016-01-01

    Highlights: • Highly oriented WO_3 stoichiometric films were determined using pulsed laser deposition method. • Effective parameters on thin films including temperature, oxygen partial pressure and laser energy fluency was studied. • A phase transition was observed in WO_3 films at 700 °C from monoclinic to tetragonal. - Abstract: WO_3 films have been grown by pulsed laser deposition on SrTiO_3 (001) substrates. The effects of substrate temperature, oxygen partial pressure and energy fluence of the laser beam on the physical properties of the films were studied. Reflection high-energy electron diffraction (RHEED) patterns during and after growth were used to determine the surface structure and morphology. The chemical composition and crystalline phases were obtained by XPS and XRD respectively. AFM results showed that the roughness and skewness of the films depend on the substrate temperature during deposition. Optimal conditions were determined for the growth of the highly oriented films.

  19. Preparation and characterization of bifunctional dendrimer modified Fe{sub 3}O{sub 4}/CdTe nanoparticles with both luminescent and superparamagnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiuling, E-mail: wxling_self@163.com [Department of Chemical and Biological Engineering, Suzhou University of Science and Technology, Suzhou 215009 (China); Gu, Yinjun; Dong, Shuling [Department of Chemical and Biological Engineering, Suzhou University of Science and Technology, Suzhou 215009 (China); Zhao, Qin [School of Chemistry and Chemical Engineering, Nantong University, Nantong, Jiangsu 226019 (China); Liu, Yongjian [Department of Chemical and Biological Engineering, Suzhou University of Science and Technology, Suzhou 215009 (China)

    2015-10-15

    Highlights: • The fluorescent superparamagnetic dendrimeric Fe{sub 3}O{sub 4}/CdTe nanoparticles are synthesized in this paper. • The synthesized nanocomposites maintain excellent magnetic properties. • The synthesized nanocomposites maintain highly luminescent markers with narrow emission bands. - Abstract: Magnetic nanoparticles Fe{sub 3}O{sub 4} were prepared by hydrothermal coprecipitation of ferric and ferrous ions using NaOH. The surface modification of Fe{sub 3}O{sub 4} nanoparticle by dendrimers has rendered the nanoparticle surface with enriched amine groups which facilitated the adsorption and conjugation of thioglycolic acid (TGA) modified CdTe quantum dots to form a stable hybrid nanostructure. Three generations (first generation: G0F, second generation: G1F, third generation: G3F) of bifunctional dendrimeric Fe{sub 3}O{sub 4}/CdTe nanoparticles were successfully prepared using this technique and characterized by microscopy. The optical and magnetic properties of the dendrimeric Fe{sub 3}O{sub 4}/CdTe nanoparticle were also investigated. The microscopic study reveals 3 different sizes for 3 generations, 16 nm (G0F), 31 nm (G1F) and 47 nm (G3F). Among three generations of nanoparticles, the G1F has the best optical property with a luminescent quantum yield of 25.6% and the G0F has the best magnetic property with a saturation magnetization of 19.3 emμ/g.

  20. Synthesis of organophosphorus modified nanoparticles and their reinforcements on the fire safety and mechanical properties of polyurea

    Energy Technology Data Exchange (ETDEWEB)

    Qian, Xiaodong [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); USTC-CityU Joint Advanced Research Centre, Suzhou Key Laboratory of Urban Public Safety, Suzhou Institute for Advanced Study, University of Science and Technology of China, 166 Ren’ai Road Suzhou, Jiangsu 215123 (China); Song, Lei, E-mail: leisong@ustc.edu.cn [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); Wang, Bibo [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); Hu, Yuan, E-mail: yuanhu@ustc.edu.cn [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); USTC-CityU Joint Advanced Research Centre, Suzhou Key Laboratory of Urban Public Safety, Suzhou Institute for Advanced Study, University of Science and Technology of China, 166 Ren’ai Road Suzhou, Jiangsu 215123 (China); Yuen, Richard K.K., E-mail: Richard.Yuen@cityu.edu.hk [USTC-CityU Joint Advanced Research Centre, Suzhou Key Laboratory of Urban Public Safety, Suzhou Institute for Advanced Study, University of Science and Technology of China, 166 Ren’ai Road Suzhou, Jiangsu 215123 (China); Department of Building and Construction, City University of Hong Kong, Tat Chee Avenue Kowloon (Hong Kong)

    2013-05-15

    Novel organophosphorus modified nanoparticles (FRs-nanoparticles) were synthesized by the hydrolysis and condensation of both 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide modified vinyl trimethoxy silane (DOPO-VTS) and 3-triethoxysilylpropylamine. FRs-nanoparticles were incorporated into the polyurea matrix in different ratios via in situ polymerization, resulting in the formation of organic/inorganic nanocomposites. The nanocomposites were characterized by thermogravimetric analysis (TGA), real-time fourier transform infrared spectra (RTIR), microscale combustion calorimeter (MCC) and tensile testing machine. The TGA results revealed that FRs-nanoparticles could slightly catalyze the thermal degradation of the nanocomposites in nitrogen atmosphere, but significantly improve the thermal stability of the nanocomposites in air atmosphere. The T{sub 0.5} (50wt.% weight loss) of the nanocomposites was delayed by 32 °C in air atmosphere. Moreover, the char yield increased from 2.3wt.% to 8.9 wt.% at 550 °C when the loadings of FRs-nanoparticles was 10wt.%, indicating the catalyzing charring effect of FRs-nanoparticles. The MCC results revealed that all the nanocomposites exhibited much lower flammability compared with virgin polyurea. Furthermore, the tensile test indicated that the FRs-nanoparticles could also improve the mechanical properties of polyurea. - Highlights: ► Novel organophosphorus modified nanoparticles (FRs-nanoparticles) were synthesized. ► FRs-nanoparticles were incorporated into the polyurea. ► Both the thermal stability and mechanical properties of polyurea were improved.

  1. Synthesis of organophosphorus modified nanoparticles and their reinforcements on the fire safety and mechanical properties of polyurea

    International Nuclear Information System (INIS)

    Qian, Xiaodong; Song, Lei; Wang, Bibo; Hu, Yuan; Yuen, Richard K.K.

    2013-01-01

    Novel organophosphorus modified nanoparticles (FRs-nanoparticles) were synthesized by the hydrolysis and condensation of both 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide modified vinyl trimethoxy silane (DOPO-VTS) and 3-triethoxysilylpropylamine. FRs-nanoparticles were incorporated into the polyurea matrix in different ratios via in situ polymerization, resulting in the formation of organic/inorganic nanocomposites. The nanocomposites were characterized by thermogravimetric analysis (TGA), real-time fourier transform infrared spectra (RTIR), microscale combustion calorimeter (MCC) and tensile testing machine. The TGA results revealed that FRs-nanoparticles could slightly catalyze the thermal degradation of the nanocomposites in nitrogen atmosphere, but significantly improve the thermal stability of the nanocomposites in air atmosphere. The T 0.5 (50wt.% weight loss) of the nanocomposites was delayed by 32 °C in air atmosphere. Moreover, the char yield increased from 2.3wt.% to 8.9 wt.% at 550 °C when the loadings of FRs-nanoparticles was 10wt.%, indicating the catalyzing charring effect of FRs-nanoparticles. The MCC results revealed that all the nanocomposites exhibited much lower flammability compared with virgin polyurea. Furthermore, the tensile test indicated that the FRs-nanoparticles could also improve the mechanical properties of polyurea. - Highlights: ► Novel organophosphorus modified nanoparticles (FRs-nanoparticles) were synthesized. ► FRs-nanoparticles were incorporated into the polyurea. ► Both the thermal stability and mechanical properties of polyurea were improved

  2. Thermomchromic Reaction-Induced Reversible Upconversion Emission Modulation for Switching Devices and Tunable Upconversion Emission Based on Defect Engineering of WO3:Yb3+,Er3+ Phosphor.

    Science.gov (United States)

    Ruan, Jiufeng; Yang, Zhengwen; Huang, Anjun; Zhang, Hailu; Qiu, Jianbei; Song, Zhiguo

    2018-05-02

    Reversible luminescence modulation of upconversion phosphors has the potential applications as photoswitches and optical memory and data storage devices. Previously, the photochromic reaction was extensively used for the realization of reversible luminescence modulation. It is very necessary to develop other approaches such as thermomchromic reaction to obtain the reversible upconversion luminescence modulation. In this work, the WO 3 :Yb 3+ ,Er 3+ phosphors with various colors were prepared at various temperatures, exhibiting tunable upconversion luminescence attributed to the formation of oxygen vacancies in the host. Upon heat treatment in the reducing atmosphere or air, the WO 3 :Yb 3+ ,Er 3+ phosphors show a reversible thermomchromic property. The reversible upconversion luminescence modulation of WO 3 :Yb 3+ ,Er 3+ phosphors was observed based on thermomchromic reaction. Additionally, the upconversion luminescence modulation is maintained after several cycles, indicating its excellent stability. The WO 3 :Yb 3+ ,Er 3+ phosphors with reversible upconversion luminescence and excellent reproducibility have potential applications as the photoswitches and optical memory and data storage devices.

  3. Enzymes immobilization on Fe 3O 4-gold nanoparticles

    Science.gov (United States)

    Kalska-Szostko, B.; Rogowska, M.; Dubis, A.; Szymański, K.

    2012-01-01

    In the present study Fe3O4 magnetic nanoparticles were synthesized by coprecipitation of Fe2+ and Fe3+ from chlorides. In the next step magnetite-gold core-shell nanoparticles were synthesized from HAuCl4 using an ethanol as a reducing agent. Finally, magnetic nanoparticles were functionalized by hexadecanethiol. The immobilization of biological molecules (trypsin and glucose oxidase) to the thiol-modified and unmodified magnetite-gold nanoparticles surface was tested. The resulting nanoparticles were characterized by infrared spectroscopy, differential scanning calorimetry, Mössbauer spectroscopy and transmission electron microscopy.

  4. 3D optical printing of piezoelectric nanoparticle-polymer composite materials.

    Science.gov (United States)

    Kim, Kanguk; Zhu, Wei; Qu, Xin; Aaronson, Chase; McCall, William R; Chen, Shaochen; Sirbuly, Donald J

    2014-10-28

    Here we demonstrate that efficient piezoelectric nanoparticle-polymer composite materials can be optically printed into three-dimensional (3D) microstructures using digital projection printing. Piezoelectric polymers were fabricated by incorporating barium titanate (BaTiO3, BTO) nanoparticles into photoliable polymer solutions such as polyethylene glycol diacrylate and exposing to digital optical masks that could be dynamically altered to generate user-defined 3D microstructures. To enhance the mechanical-to-electrical conversion efficiency of the composites, the BTO nanoparticles were chemically modified with acrylate surface groups, which formed direct covalent linkages with the polymer matrix under light exposure. The composites with a 10% mass loading of the chemically modified BTO nanoparticles showed piezoelectric coefficients (d(33)) of ∼ 40 pC/N, which were over 10 times larger than composites synthesized with unmodified BTO nanoparticles and over 2 times larger than composites containing unmodified BTO nanoparticles and carbon nanotubes to boost mechanical stress transfer efficiencies. These results not only provide a tool for fabricating 3D piezoelectric polymers but lay the groundwork for creating highly efficient piezoelectric polymer materials via nanointerfacial tuning.

  5. Synthesis and characterization of MoO3WO3 composite thin films ...

    Indian Academy of Sciences (India)

    Abstract. In order to achieve high colouration efficiency, MoO3WO3 composite thin films have been successfully deposited on sodium silicate glass and silicon wafer (111) at 30 ◦C by a very simple novel wet process known as liquid phase deposition. The deposited films were annealed at different temperatures and ...

  6. Promotion effect of Pt on a SnO2-WO3 material for NOx sensing

    Science.gov (United States)

    Wang, Chen-Yang; Hong, Zih-Siou; Wu, Ren-Jang

    2015-05-01

    Metal-oxide nanocomposites were prepared over screen-printed gold electrodes to be used as room-temperature NOx (nitric-oxide (NO) and nitrogen dioxide (NO2)) sensors. Various weight ratios of SnO2-WO3 and Pt loadings were used for NO sensing. The sensing materials were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET surface analysis. The NO-sensing results indicated that SnO2-WO3 (1:2) was more effective than other materials were. The sensor response (S=resistance of N2/resistance of NO=RN2/RNO) for detecting 1000 ppm of NO at room temperature was 2.6. The response time (T90) and recovery time (TR90) was 40 s and 86 s, respectively. By further loading with 0.5% Pt, the sensor response increased to 3.3. The response and recovery times of 0.5% Pt/SnO2-WO3 (1:2) were 40 s and 206 s, respectively. The linearity of the sensor response for a NO concentration range of 10-1000 ppm was 0.9729. A mechanism involving Pt promotion of the SnO2-WO3 heterojunction was proposed for NO adsorption, surface reaction, and adsorbed NO2 desorption.

  7. Polyethyleneimine-modified superparamagnetic Fe3O4 nanoparticles: An efficient, reusable and water tolerance nanocatalyst

    International Nuclear Information System (INIS)

    Khoobi, Mehdi; Delshad, Tayebeh Modiri; Vosooghi, Mohsen; Alipour, Masoumeh; Hamadi, Hosein; Alipour, Eskandar; Hamedani, Majid Pirali; Sadat ebrahimi, Seyed Esmaeil; Safaei, Zahra; Foroumadi, Alireza; Shafiee, Abbas

    2015-01-01

    A novel magnetically separable catalyst was prepared based on surface modification of Fe 3 O 4 magnetic nanoparticle (MNPs) with polyethyleneimine (PEI) via covalent bonding. [3-(2,3-Epoxypropoxy)propyl]trimethoxysilane (EPO) was used as cross linker to bond PEI on the surface of MNPs with permanent stability in contrast to PEI coating via electrostatic interactions. The synthesized catalyst was characterized by Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), X-ray powder diffraction (XRD), transmission electron microscopy (TEM) and vibrating sample magnetometry (VSM). The catalyst show high efficiency for one-pot synthesis of 2-amino-3-cyano-4H-pyran derivatives via multi-component reaction (MCR). This procedure offers the advantages of green reaction media, high yield, short reaction time, easy purification of the products and simple recovery and reuse of the catalyst by simple magnetic decantation without significant loss of catalytic activity. - Graphical abstract: Covalently grafted polyethyleneimine on Fe 3 O 4 magnetic nanoparticles as easily reusable catalyst for the synthesis of various 4H-pyrans. - Highlights: • Polyethyleneimine modified Fe 3 O 4 via covalent bonding as a novel water tolerance catalyst. • The catalyst showed high efficiency for one-pot synthesis of 2-amino-3-cyano-4H-pyrans in water. • Catalysts could be easily recovered and reused for several times without a significant loss in their catalytic activity

  8. Dipodal Silane-modified Nano Fe3O4/Polyurethane Magnetic Nanocomposites: Preparation and Characterization

    OpenAIRE

    Mir Mohammad Alavi Nikje; Maryam Vakili; Reihaneh Farajollah; Raheleh Akbar; Moslem Haghshenas

    2016-01-01

    Magnetic nanocomposites were prepared by incorporation of pure Fe3O4 and surface-modified Fe3O4 nanoparticles (dipodal silane-modified Fe3O4) into a polyurethane elastomer matrix by in situ polymerization method. In preparation of these magnetic nanocomposites, polycaprolactone (PCL) was used as a polyester polyol. Because of dipole-dipole interactions between nanoparticles and a large surface area to volume ratio, the magnetic iron oxide nanoparticles tended to agglomerate. Furthermore, the ...

  9. AC conductivity and dielectric properties of bulk tungsten trioxide (WO3)

    Science.gov (United States)

    El-Nahass, M. M.; Ali, H. A. M.; Saadeldin, M.; Zaghllol, M.

    2012-11-01

    AC conductivity and dielectric properties of tungsten trioxide (WO3) in a pellet form were studied in the frequency range from 42 Hz to 5 MHz with a variation of temperature in the range from 303 K to 463 K. AC conductivity, σac(ω) was found to be a function of ωs where ω is the angular frequency and s is the frequency exponent. The values of s were found to be less than unity and decrease with increasing temperature, which supports the correlated barrier hopping mechanism (CBH) as the dominant mechanism for the conduction in WO3. The dielectric constant (ε‧) and dielectric loss (ε″) were measured. The Cole-Cole diagram determined complex impedance for different temperatures.

  10. Structure and frictional properties of Langmuir-Blodgett films of Cu nanoparticles modified by dialkyldithiophosphate

    International Nuclear Information System (INIS)

    Xu Jun; Dai Shuxi; Cheng Gang; Jiang Xiaohong; Tao Xiaojun; Zhang Pingyu; Du Zuliang

    2006-01-01

    Langmuir-Blodgett (LB) films of dialkyldithiophosphate (DDP) modified Cu nanoparticles were prepared. The structure, microfrictional behaviors and adhesion of the LB films were investigated by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and atomic/friction force microscopy (AFM/FFM). Our results showed that the modified Cu nanoparticles have a typical core-shell structure and fine film-forming ability. The images of AFM/FFM showed that LB films of modified Cu nanoparticles were composed of many nanoparticles arranged closely and orderly and the nanoparticles had favorable behaviors of lower friction. The friction loop of the films indicated that the friction force was affected prominently by the surface slope of the Cu nanoparticles and the microfrictional behaviors showed obvious 'ratchet effect'. The adhesion experiment showed that the modified Cu nanoparticle had a very small adhesive force

  11. Characterization of nanoparticles of lidocaine in w/o microemulsions ...

    Indian Academy of Sciences (India)

    drophilic phase and a hydrophobic phase, stabilized with the use of surfactants. Regular MEs consist of nanometer-sized hydrocarbon domains (termed micelles) surrounded by amphiphilic molecules, stabilized in a continuous aqueous phase. In contrast, reverse (w/o) MEs consist of aqueous domains (termed reverse ...

  12. Electrocatalytic Performance of Carbon Supported WO3-Containing Pd–W Nanoalloys for Oxygen Reduction Reaction in Alkaline Media

    Directory of Open Access Journals (Sweden)

    Nan Cui

    2018-05-01

    Full Text Available In this paper, we report that WOx containing nanoalloys exhibit stable electrocatalytic performance in alkaline media, though bulk WO3 is easy to dissolve in NaOH solution. Carbon supported oxide-rich Pd–W alloy nanoparticles (PdW/C with different Pd:W atom ratios were prepared by the reduction–oxidation method. Among the catalysts, the oxide-rich Pd0.8W0.2/C (Pd/W = 8:2, atom ratio exhibits the highest catalytic activity for the oxygen reduction reaction. The X-ray photoelectron spectroscopy data shows that ~40% of Pd atoms and ~60% of the W atoms are in their oxide form. The Pd 3d5/2 binding energy of the oxide-rich Pd–W nanoalloys is higher than that of Pd/C, indicating the electronic structure of Pd is affected by the strong interaction between Pd and W/WO3. Compare to Pd/C, the onset potential of the oxygen reduction reaction at the oxide-rich Pd0.8W0.2/C shifts to a higher potential. The current density (mA·mg Pd−1 at the oxide-rich Pd0.8W0.2/C is ~1.6 times of that at Pd/C. The oxide-rich Pd0.8W0.2/C also exhibits higher catalytic stability than Pd/C, which demonstrates that it is a prospective candidate for the cathode of fuel cells operating with alkaline electrolyte.

  13. Synthesis of γ-WO{sub 3} thin films by hot wire-CVD and investigation of its humidity sensing properties

    Energy Technology Data Exchange (ETDEWEB)

    Jadkar, Vijaya; Waykar, Ravindra; Jadhavar, Ashok [School of Energy Studies, Savitribai Phule Pune University, Pune 411 007 (India); Pawbake, Amit [School of Energy Studies, Savitribai Phule Pune University, Pune 411 007 (India); Physical and Material Chemistry Division, National Chemical Laboratory, Pune 411 008 (India); Date, Abhijit [School of Aerospace, Mechanical and Manufacturing Engineering, RMIT University, Plenty Road, Bundoora, Melbourne VIC 3083 (Australia); Late, Dattatray [Physical and Material Chemistry Division, National Chemical Laboratory, Pune 411 008 (India); Pathan, Habib; Gosavi, Suresh; Jadkar, Sandesh [Department of Physics, Savitribai Phule Pune University, Pune 411 007 (India)

    2017-05-15

    In this study, monoclinic tungsten oxide (γ-WO{sub 3}) have been grown in a single step using HW-CVD method by resistively heating W filaments in a constant O{sub 2} pressure. The formation of γ-WO{sub 3} was confirmed using low angle-XRD and Raman spectroscopy analysis. Low angle-XRD analysis revealed that as-deposited WO{sub 3} film are highly crystalline and the crystallites have preferred orientation along the (002) direction. HRTEM analysis and SAED pattern also show the highly crystalline nature of WO{sub 3} with d spacing of ∝ 0.38 nm, having an orientation along the (002) direction. Surface topography investigated by SEM analysis shows the formation of a uniform and homogeneous cauliflower like morphology throughout the substrate surface without flaws and cracks. A humidity sensing device incorporating WO{sub 3} is also fabricated, which shows a maximum humidity sensitivity factor of ∝ 3954% along with a response time of ∝14 s and a recovery time of ∝25 s. The obtained results demonstrate that it is possible to synthesize WO{sub 3} in a single step by HW-CVD method and to fabricate a humidity sensor by using it. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Fluorescence immunoassay for detecting periodontal bacterial pathogens in plaque.

    OpenAIRE

    Wolff, L F; Anderson, L; Sandberg, G P; Aeppli, D M; Shelburne, C E

    1991-01-01

    A particle concentration fluorescence immunoassay has been modified into a bacterial concentration fluorescence immunoassay (BCFIA) to rapidly detect periodontopathic bacteria in human plaque samples. The BCFIA utilizes fluorescently tagged monoclonal antibodies (MAbs) directed against the lipopolysaccharide of selected gram-negative plaque bacteria. Microorganisms closely associated with periodontal disease that can be identified in plaque with the BCFIA include Porphyromonas gingivalis, Bac...

  15. Fabrication and Luminescent properties of ZnWO{sub 4}:Eu{sup 3+}, Dy{sup 3+} white light-emitting phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Zhai, Yongqing, E-mail: zhaiyongqinghbu@163.com; Wang, Meng; Zhao, Qian; Yu, Jiabao; Li, Xuemin

    2016-04-15

    ZnWO{sub 4}:Eu{sup 3+},Dy{sup 3+} white light-emitting phosphors were prepared by a hydrothermal method followed with calcination process. The as-synthesized phosphors were characterized by X-ray powder diffraction (XRD), Fourier transform infrared (FTIR) spectrum, Raman spectra, scanning electron microscope (SEM), transmission electron microscope (TEM), diffused reflectance spectra, photoluminescence excitation and emission spectra, and photoluminescence decay curves. Furthermore, external quantum efficiency of ZnWO{sub 4}:Eu{sup 3+},Dy{sup 3+} was determined. The results showed that the obtained phosphors have monoclinic wolframite structure. The particles of the phosphors was nearly spherical in shape, and the particle size was about 70–100 nm. Upon excitation at UV light, the white light-emitting can be obtained by combining the blue–green emission of tungstate group and characteristic emission of Eu{sup 3+} and Dy{sup 3+}. Based on the excitation/emission spectra and decay curves, the energy transfer and photoluminescence mechanism for ZnWO{sub 4}:Eu{sup 3+}, Dy{sup 3+} system were discussed.

  16. A single-phase white light emitting Pr3+ doped Ba2CaWO6 phosphor: synthesis, photoluminescence and optical properties

    Science.gov (United States)

    Sreeja, E.; Vidyadharan, Viji; Jose, Saritha K.; George, Anns; Joseph, Cyriac; Unnikrishnan, N. V.; Biju, P. R.

    2018-04-01

    Pr3+ doped Ba2CaWO6 phosphor were prepared by traditional high-temperature solid-state reaction technique. The structure evolution was systematically investigated by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analysis. The X-ray powder diffraction patterns indicate that the prepared phosphors crystallized in the cubic double-perovskite structure. The functional groups were identified using FTIR spectra and the elements present in the composition were confirmed by the EDS profile. The morphology of the phosphor was identified using SEM and TEM analysis. The PL spectra illustrated that these phosphors could be efficiently excited by charge transfer band of host and the maximum luminescence intensity was observed at 0.06 wt% of Pr3+ ion. Upon the charge transfer band excitation, emission spectra showed peaks at 489, 532, 647, 685 and 737 nm corresponding to 3P0→3H4, 3P1→3H5, 3P0→3F2, 3P0→3F3 and 3P0→3F4 transitions respectively. The concentration quenching of Ba2CaWO6:Pr3+ phosphor can be mainly attributed to dipole-dipole interaction. The CIE coordinates were estimated to be close to the white region. The decay curves are well fitted with double exponential decay models. The standard and modified Judd-Ofelt (JO) theories were used to determine the Judd-Ofelt intensity parameters, radiative transition probabilities and branching ratios. The optical properties indicate that Ba2CaWO6:Pr3+ phosphors can produce white light emission from a single phase host and its potential application for solid-state lighting and display devices.

  17. Enhanced Water Oxidation Photoactivity of Nano-Architectured α-Fe2O3-WO3 Composite Synthesized by Single-Step Hydrothermal Method

    Science.gov (United States)

    Rahman, Gul; Joo, Oh-Shim; Chae, Sang Youn; Shah, Anwar-ul-Haq Ali; Mian, Shabeer Ahmad

    2018-04-01

    This study reports the one-step in situ synthesis of a hematite-tungsten oxide (α-Fe2O3-WO3) composite on fluorine-doped tin oxide substrate via a simple hydrothermal method. Scanning electron microscopy images indicated that the addition of tungsten (W) precursor into the reaction mixture altered the surface morphology from nanorods to nanospindles. Energy-dispersive x-ray spectroscopy analysis confirmed the presence of W content in the composite. From the ultraviolet-visible spectrum of α-Fe2O3-WO3, it was observed that absorption began at ˜ 600 nm which corresponded to the bandgap energy of ˜ 2.01 eV. The α-Fe2O3-WO3 electrode demonstrated superior performance, with water oxidation photocurrent density of 0.80 mA/cm2 (at 1.6 V vs. reversible hydrogen electrode under standard illumination conditions; AM 1.5G, 100 mW/cm2) which is 2.4 times higher than α-Fe2O3 (0.34 mA/cm2). This enhanced water oxidation performance can be attributed to the better charge separation properties in addition to the large interfacial area of small-sized particles present in the α-Fe2O3-WO3 nanocomposite film.

  18. Ethanol vapour sensing properties of screen printed WO3 thick films

    Indian Academy of Sciences (India)

    TECS

    trations. The WO3 thick films exhibit excellent ethanol vapour sensing properties with a maximum sensitivity ... methanol, acetone, isopropanol and acetic acid, have been reported .... maximum sensitivity was obtained at an operating tem-.

  19. Cerium oxide-deposited mesoporous silica nanoparticles for the determination of carcinoembryonic antigen in serum using inductively coupled plasma-mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Choi, H.W. [Department of Chemistry, NSBI, Dankook University, 126 Jukjeon-dong, Suji-gu, Yongin-si, Gyeonggi-do 448-701 (Korea, Republic of); Lee, K.H.; Hur, N.H. [Department of Chemistry, Sogang University, Shinsu-dong, Mapo-gu, Seoul (Korea, Republic of); Lim, H.B., E-mail: plasma@dankook.ac.kr [Department of Chemistry, NSBI, Dankook University, 126 Jukjeon-dong, Suji-gu, Yongin-si, Gyeonggi-do 448-701 (Korea, Republic of)

    2014-10-17

    Highlights: • Sandwich-type immunoassay using ICP-MS and nanoparticles to determine biomarkers. • CeO{sub 2}-deposited mesoporous silica nanoparticles were synthesized as a probe. • Ratiometric measurement significantly improved the calibration linearity. • Excellent detection limit was achieved by signal amplification. - Abstract: CeO{sub 2}-deposited mesoporous silica nanoparticles were synthesized as a probe to determine carcinoembryonic antigen (CEA) in serum by inductively coupled plasma-mass spectrometry (ICP-MS). The prepared mesoporous nanoparticles were modified and tagged to the target for sandwich-type immunoassay. Fe{sub 3}O{sub 4} magnetic nanoparticles (MNPs) were also synthesized and immobilized with antibody to extract the target biomarker. The calibration curve of the synthesized CeO{sub 2}-deposited silica nanoparticles, which was plotted by the signal ratio of {sup 140}Ce/{sup 57}Fe measured by ICP-MS vs. the concentration of CEA, showed excellent linearity and sensitivity owing to the signal amplification and low spectral interference. Under optimal conditions, the sandwich-type analytical method was applied to determine CEA in serum spiked in the range of 0.001–5 ng mL{sup −1} and showed a limit of detection of 0.36 ng mL{sup −1}. Since the deposited CeO{sub 2} in the mesoporous silica layer can be substituted by other metal compounds, various kinds of metal-deposited nanoparticles can be prepared as probe materials for multiplex detection in bioanalysis.

  20. Synthesis, formation mechanism and sensing properties of WO3 hydrate nanowire netted-spheres

    International Nuclear Information System (INIS)

    Yan, Aihua; Xie, Changsheng; Zeng, Dawen; Cai, Shuizhou; Hu, Mulin

    2010-01-01

    Tungsten oxide hydrate nanowire netted-spheres were successfully synthesized in the glycol solution using a facile solvothermal approach. The nanowires with uniform diameter of 4-6 nm are actually a kind of tungsten oxide hydrate/surfactant hybrid materials. The influence of surfactant, solvent, time and temperature on tailoring morphology was investigated in detail. The possible formation process of WO 3 hydrate nanowire netted-sphere was proposed. Sensing properties of such WO 3 hydrate sensor show that the desirable sensing characteristics towards 100 ppm ammonia gas at 320 o C were obtained, such as rapid response (18.3 s), high sensitivity, good reproducibility and stability.

  1. Thermal properties and optical transition probabilities of Tm3 + doped TeO2-WO3 glass.

    Science.gov (United States)

    Cenk, S; Demirata, B; Oveçoglu, M L; Ozen, G

    2001-10-01

    Glasses with the composition of (1 - x)TeO2 + (x)WO3, where x = 0.15, 0.25 and 0.3 were prepared and, their thermal and absorption measurements were carried out. Differential thermal analysis (DTA) curves taken in the 23-600 degrees C temperature range with a heating rate of 10 degrees C/min reveal a change in the value of the glass transition temperature, Tg, while crystallization was not observed for the glasses containing a WO3 content of more than 15 mol%. All the glasses were found to be moisture-resistant. The absorption bands corresponding to the absorption of the 1G4, 3F2, 3F3 and 3F4, 3H5 and 3H4 levels from the 3H6 ground level of the Tm3+ ion were observed in the optical absorption spectra. Integrated absorption cross-sections of each band except that of 3H5 level was found to vary with the glass composition. Judd-Ofelt analysis was carried out for the samples doped with 1.0 mol% Tm2O3. The omega2 parameter shows the strongest dependence on the host composition and it increases with the increasing WO3 amount. The value of omega4 increases rather slowly while the value of omega6 is practically independent of the composition. The strong dependence of the parameter omega2 indicates that this parameter is related to the structural change and the symmetry of the local environment of the Tm3+ ions in this glass.

  2. Modified Polymeric Nanoparticles Exert In Vitro Antimicrobial Activity Against Oral Bacteria.

    Science.gov (United States)

    Toledano-Osorio, Manuel; Babu, Jegdish P; Osorio, Raquel; Medina-Castillo, Antonio L; García-Godoy, Franklin; Toledano, Manuel

    2018-06-14

    Polymeric nanoparticles were modified to exert antimicrobial activity against oral bacteria. Nanoparticles were loaded with calcium, zinc and doxycycline. Ions and doxycycline release were measured by inductively coupled plasma optical emission spectrometer and high performance liquid chromatography. Porphyromonas gingivalis , Lactobacillus lactis , Streptoccocus mutans , gordonii and sobrinus were grown and the number of bacteria was determined by optical density. Nanoparticles were suspended in phosphate-buffered saline (PBS) at 10, 1 and 0.1 mg/mL and incubated with 1.0 mL of each bacterial suspension for 3, 12, and 24 h. The bacterial viability was assessed by determining their ability to cleave the tetrazolium salt to a formazan dye. Data were analyzed by ANOVA and Scheffe’s F ( p Nanoparticles (60% to 99% reduction) followed by Ca-Nanoparticles or Zn-Nanoparticles (30% to 70% reduction) and finally the non-doped nanoparticles (7% to 35% reduction). P. gingivalis , S. mutans and L. lactis were the most susceptible bacteria, being S. gordonii and S. sobrinus the most resistant to the tested nanoparticles.

  3. Metal-doped inorganic nanoparticles for multiplex detection of biomarkers by a sandwich-type ICP-MS immunoassay.

    Science.gov (United States)

    Ko, Jung Aa; Lim, H B

    2016-09-28

    Metal-doped inorganic nanoparticles were synthesized for the multiplex detection of biomarkers by a sandwich-type inductively coupled plasma mass spectrometry (ICP-MS) immunoassay. The synthesized Cs-doped multicore magnetic nanoparticles (MMNPs) were used not only for magnetic extraction of targets but also for ratiometric measurement in ICP-MS. In addition, three different metal/dye-doped silica nanoparticles (SNPs) were synthesized as probes for multiplex detection: Y/RhBITC (rhodamine B isothiocyanate)-doped SNPs for CRP (cardiovascular disease), Cd/RhBITC-doped SNPs for AFP (tumor), and Au/5(6)-XRITC (X-rhodamine-5-(and-6)-isothiocyanate)-doped SNPs for NSE (heart disease). For quantification, the doped metals of SNPs were measured by ICP-MS and then the signal ratio to Cs of MMNPs was plotted with respect to the concentration of targets by a ratiometry. Limits of detection (LOD) of 0.35 ng/mL to 77 ng mL(-1) and recoveries of 83%-125% were obtained for serum samples spiked with the biomarkers. Since no sample treatment was necessary prior to the extraction, the proposed method provided short analysis time and convenience for the multiplex determination of biomarkers, which will be valuable for clinical application. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. Electrochemiluminescence immunosensor for ultrasensitive detection of biomarker using Ru(bpy)(3)(2+)-encapsulated silica nanosphere labels.

    Science.gov (United States)

    Qian, Jing; Zhou, Zhenxian; Cao, Xiaodong; Liu, Songqin

    2010-04-14

    Here, we describe a new approach for electrochemiluminescence (ECL) assay with Ru(bpy)(3)(2+)-encapsulated silica nanoparticle (SiO(2)@Ru) as labels. A water-in-oil (W/O) microemulsion method was employed for one-pot synthesis of SiO(2)@Ru nanoparticles. The as-synthesized SiO(2)@Ru nanoparticles have a narrow size distribution, which allows reproducible loading of Ru(bpy)(3)(2+) inside the silica shell and of alpha-fetoprotein antibody (anti-AFP), a model antibody, on the silica surface with glutaraldehyde as linkage. The silica shell effectively prevents leakage of Ru(bpy)(3)(2+) into the aqueous solution due to strong electrostatic interaction between the positively charged Ru(bpy)(3)(2+) and the negatively charged surface of silica. The porous structure of silica shell allowed the ion to move easily through the pore to exchange energy/electrons with the entrapped Ru(bpy)(3)(2+). The as-synthesized SiO(2)@Ru can be used as a label for ultrasensitive detection of biomarkers through a sandwiched immunoassay process. The calibration range of AFP concentration was 0.05-30 ng mL(-1) with linear relation from 0.05 to 20 ng mL(-1) and a detection limit of 0.035 ng mL(-1) at 3sigma. The resulting immunosensors possess high sensitivity and good analytical performance. Copyright 2010 Elsevier B.V. All rights reserved.

  5. A novel orange emissive phosphor SrWO4:Sm3+ for white light-emitting diodes

    International Nuclear Information System (INIS)

    Ju Zhenghua; Wei Ruiping; Ma Jingxin; Pang Chaoran; Liu Weisheng

    2010-01-01

    Research highlights: → A novel orange emissive phosphor SrWO 4 :Sm 3+ was firstly reported. → The optics properties of Sm 3+ -doped SrWO 4 phosphor were successfully discussed. → The temperature-dependent luminescence indicates the phosphor exhibits a small thermal-quenching property. → The phosphor is a potential candidate as orange-emitting component for white LED. - Abstract: A novel orange emissive phosphor, Sm 3+ -doped SrWO 4 , was synthesized by high temperature solid-state reaction in air atmosphere. The excitation spectra show that the phosphors can be efficiently excited by ultraviolet and near-ultraviolet light, the optimized concentration is 4 mol%. Three emission peaks locate at 562, 596 and 642 nm, corresponding to CIE chromaticity coordinates of (x = 0.54, y = 0.46), which indicates the orange light emitting. The decay curves are well fitted with triple-exponential decay models. The quantum yield of the Sr 0.96 Sm 0.04 WO 4 phosphor is about 70.65% under excitation of 377 nm. Furthermore, the temperature-dependent luminescence indicates the phosphor exhibits a small thermal-quenching property. So the phosphor is able to be applied to UV-LED chip-based white light-emitting diodes.

  6. Understanding the conductive channel evolution in Na:WO3-x-based planar devices

    Science.gov (United States)

    Shang, Dashan; Li, Peining; Wang, Tao; Carria, Egidio; Sun, Jirong; Shen, Baogen; Taubner, Thomas; Valov, Ilia; Waser, Rainer; Wuttig, Matthias

    2015-03-01

    An ion migration process in a solid electrolyte is important for ion-based functional devices, such as fuel cells, batteries, electrochromics, gas sensors, and resistive switching systems. In this study, a planar sandwich structure is prepared by depositing tungsten oxide (WO3-x) films on a soda-lime glass substrate, from which Na+ diffuses into the WO3-x films during the deposition. The entire process of Na+ migration driven by an alternating electric field is visualized in the Na-doped WO3-x films in the form of conductive channel by in situ optical imaging combined with infrared spectroscopy and near-field imaging techniques. A reversible change of geometry between a parabolic and a bar channel is observed with the resistance change of the devices. The peculiar channel evolution is interpreted by a thermal-stress-induced mechanical deformation of the films and an asymmetric Na+ mobility between the parabolic and the bar channels. These results exemplify a typical ion migration process driven by an alternating electric field in a solid electrolyte with a low ion mobility and are expected to be beneficial to improve the controllability of the ion migration in ion-based functional devices, such as resistive switching devices.An ion migration process in a solid electrolyte is important for ion-based functional devices, such as fuel cells, batteries, electrochromics, gas sensors, and resistive switching systems. In this study, a planar sandwich structure is prepared by depositing tungsten oxide (WO3-x) films on a soda-lime glass substrate, from which Na+ diffuses into the WO3-x films during the deposition. The entire process of Na+ migration driven by an alternating electric field is visualized in the Na-doped WO3-x films in the form of conductive channel by in situ optical imaging combined with infrared spectroscopy and near-field imaging techniques. A reversible change of geometry between a parabolic and a bar channel is observed with the resistance change of the

  7. Luminescence and photothermally stimulated defects creation processes in PbWO{sub 4}:La{sup 3+}, Y{sup 3+} (PWO II) crystals

    Energy Technology Data Exchange (ETDEWEB)

    Auffray, E. [CERN, Geneva 23, Geneva (Switzerland); Korjik, M. [Institute for Nuclear Problems, 11 Bobruiskaya, 220020 Minsk (Belarus); Zazubovich, S., E-mail: svetlana.zazubovits@ut.ee [Institute of Physics, University of Tartu, Ravila 14 c, 50411 Tartu (Estonia)

    2015-12-15

    Photoluminescence and thermally stimulated luminescence (TSL) are studied for a PbWO{sub 4} crystal grown by the Czochralski method at Bogoroditsk Technical Chemical Plant, Russia from the melt with a precise tuning of the stoichiometry and co-doped with La{sup 3+} and Y{sup 3+} ions (the PWO II crystal). Photothermally stimulated processes of electron and hole centers creation under selective UV irradiation of this crystal in the 3.5–5.0 eV energy range and the 85–205 K temperature range are clarified and the optically created electron and hole centers are identified. The electrons in PWO II are mainly trapped at the (WO{sub 4}){sup 2−} groups located close to single La{sup 3+} and Y{sup 3+} ions, producing the electron {(WO_4)"3"−–La"3"+} and {(WO_4)"3"−–Y"3"+} centers. The holes are mainly trapped at the regular oxygen ions O{sup 2−} located close to La{sup 3+} and Y{sup 3+} ions associated with lead vacancies, producing the hole O{sup −}(I)-type centers. No evidence of single-vacancy-related centers has been observed in PWO II. The data obtained indicate that excellent scintillation characteristics of the PWO II crystal can be explained by a negligible concentration of single (non-compensated) oxygen and lead vacancies as the traps for electrons and holes, respectively. - Highlights: • Photoluminescence of the PbWO{sub 4}:La{sup 3+}, Y{sup 3+} (PWO II) crystal is investigated. • Creation of defects under UV irradiation of PWO II is studied by TSL. • Origin of dominating electron and hole centers is ascertained. • Concentration of single-vacancy-related centers is found to be negligible. • Excellent scintillation characteristics of the PWO II crystal are explained.

  8. Synthesis and photoluminescence properties of Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped Ca{sub 2}ZnWO{sub 6} phosphors for phosphor converted LED

    Energy Technology Data Exchange (ETDEWEB)

    Dabre, K.V. [Department of Physics, Arts, Commerce and Science College, Koradi, Nagpur-441111, Maharashtra (India); Dhoble, S.J., E-mail: sjdhoble@rediffmail.com [Department of Physics, R.T.M. Nagpur University, Nagpur-440033, Maharashtra (India)

    2014-06-01

    In this work, we report on the synthesis and photoluminescence (PL) properties of rare earth (Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+}) doped double perovskite tungstate Ca{sub 2}ZnWO{sub 6} phosphor. The phosphors were synthesized by two step modified solid state method. Phase purity and formation of phosphor were confirmed by XRD technique. PL spectra of Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped phosphor show intense emission peaks in red region at 615, 604 and 650 nm respectively, upon the visible excitation of 466 nm (Eu{sup 3+}), 410 nm (Sm{sup 3+}) and 491 nm (Pr{sup 3+}). The CIE coordinates of the phosphors are in the yellow (Sm{sup 3+} doped sample) and orange (Eu{sup 3+} and Pr{sup 3+} doped sample) regions near the edge of color space which confirms their applicability in LEDs. -- Highlights: •Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped and undoped samples of Ca{sub 2}ZnWO{sub 6} phosphor synthesized by Solid state method. •The phosphors have intense excitation in violet and blue region of visible spectrum. •Phosphors show intense emission peaks in red region. •CIE coordinates of phosphors are lie in yellow (Sm{sup 3+} doped phosphor) and orange (Eu{sup 3+} and Pr{sup 3+} doped phosphor) region near to edge of color space.

  9. Improvement of β-phase crystal formation in a BaTiO3-modified PVDF membrane

    Science.gov (United States)

    Lin, SHEN; Lei, GONG; Shuhua, CHEN; Shiping, ZHAN; Cheng, ZHANG; Tao, SHAO

    2018-04-01

    In this paper, low temperature plasma is used to modify the surface of barium titanate (BaTiO3) nanoparticles in order to enhance the interfacial compatibility between ferroelectric poly(vinylidene fluoride) (PVDF) and BaTiO3 nanoparticles. The results demonstrate that oxygenic groups are successfully attached to the BaTiO3 surface, and the quantity of the functional groups increases with the treatment voltage. Furthermore, the effect of modified BaTiO3 nanoparticles on the morphology and crystal structure of the PVDF/BaTiO3 membrane is investigated. The results reveal that the dispersion of BaTiO3 nanoparticles in the PVDF matrix was greatly improved due to the modification of the BaTiO3 nanoparticles by air plasma. It is worth noting that the formation of a β-phase in a PVDF/modified BaTiO3 membrane is observably promoted, which results from the strong interaction between PVDF chains and oxygenic groups fixed on the BaTiO3 surface and the better dispersion of BaTiO3 nanoparticles in the PVDF matrix. Besides, the PVDF/modified BaTiO3 membrane at the treatment voltage of 24 kV exhibits a lower water contact angle (≈68.4°) compared with the unmodified one (≈86.7°). Meanwhile, the dielectric constant of PVDF/BaTiO3 nanocomposites increases with the increase of working voltage.

  10. Application of Nanostructures in Electrochromic Materials and Devices: Recent Progress

    Directory of Open Access Journals (Sweden)

    Jin Min Wang

    2010-11-01

    Full Text Available The recent progress in application of nanostructures in electrochromic materials and devices is reviewed. ZnO nanowire array modified by viologen and WO3, crystalline WO3 nanoparticles and nanorods, mesoporous WO3 and TiO2, poly(3,4-ethylenedioxythiophene nanotubes, Prussian blue nanoinks and nanostructures in switchable mirrors are reviewed. The electrochromic properties were significantly enhanced by applying nanostructures, resulting in faster switching responses, higher stability and higher optical contrast. A perspective on the development trends in electrochromic materials and devices is also proposed.

  11. Dot immunoassay for the simultaneous determination of postvaccination immunity against pertussis, diphtheria, and tetanus.

    Science.gov (United States)

    Khramtsov, Pavel; Bochkova, Maria; Timganova, Valeria; Zamorina, Svetlana; Rayev, Mikhail

    2017-06-01

    A dot immunoassay for simultaneous semiquantitative detection of IgG against tetanus toxoid (Ttx) and diphtheria toxoid (Dtx) and qualitative detection of anti-Bordetella pertussis IgGs in human blood serum using carbon nanoparticles functionalized with streptococcal protein G was developed. Inactivated B. pertussis cells in suspension form were used as an antigen in the immunoassay. Pertussis, tetanus, and diphtheria antigens were separately spotted onto nitrocellulose strips, and then the immunostrips were successively incubated with blood sera and a suspension of carbon nanoparticles. The immunostrips were then scanned with a flatbed scanner, and the images obtained were processed with ImageJ. One hundred fifty-five venous blood serum samples from children vaccinated with diphtheria, tetanus, and whole-cell pertussis (DTwP) vaccine were tested in comparison with a conventional ELISA and agglutination test. The total time required for analysis of 32 serum samples was less than 3 h. Comparison between the results of the dot immunoassay and the corresponding ELISA/agglutination test revealed a high level of agreement (Cohen's kappa between 0.765 and 0.813). The lower limit of quantification was 0.06 IU/ml for anti-Ttx and anti-Dtx. The intra-assay coefficients of variation were less than 15% for anti-Ttx and anti-Dtx and less than 10% for anti-pertussis. The diagnostic sensitivity of detection of the antibody protection level was 93.5% for anti-Ttx [95% confidence interval (CI) 83.5-97.9%], 92.4% for anti-Dtx (95% CI 80.9297.5%), and 90.2% for anti-pertussis (95% CI 75.9-96.8%). The diagnostic specificity was 90.9% for anti-Ttx (95% CI 57.1-99.5%), 85% for anti-Dtx (95% CI 61.1-96.0%), and 89.3% for anti-pertussis (95%CI 80.8-94.5%). The dot immunoassay developed does not require expensive reading equipment, and allows detection of antibodies against three antigens in a single analysis. The immunostrips can be stored for a long time without changes in the

  12. Experimental study of mutagenous and mitosis modifying activity of silver nanoparticles

    Directory of Open Access Journals (Sweden)

    B. S. Kirbik

    2015-01-01

    Full Text Available Mutagenous and mitosis modifying impact of silver nanoparticles has been studied on outbred mice. Nanoparticles were of round shape with dimensions of 5-50 nm, size of generated organic shell of 2-5 nm, th