Structural, optical, and magnetic properties of Fe doped In{sub 2}O{sub 3} powders

Energy Technology Data Exchange (ETDEWEB)

Krishna, N. Sai [Thin Films Laboratory, School of Advanced Sciences, VIT University, Vellore 632 014, Tamilnadu (India); Kaleemulla, S., E-mail: skaleemulla@gmail.com [Thin Films Laboratory, School of Advanced Sciences, VIT University, Vellore 632 014, Tamilnadu (India); Amarendra, G. [Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102, Tamilnadu (India); UGC-DAE-CSR, Kalpakkam Node, Kokilamedu 603 104, Tamilnadu (India); Rao, N. Madhusudhana; Krishnamoorthi, C.; Kuppan, M.; Begam, M. Rigana [Thin Films Laboratory, School of Advanced Sciences, VIT University, Vellore 632 014, Tamilnadu (India); Reddy, D. Sreekantha [Department of Physics and Sungkyunkwan Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 440-746 (Korea, Republic of); Omkaram, I. [Department of Electronics and Radio Engineering, Kyung Hee University, Yongin-si, Gyeonggi-do 446-701 (Korea, Republic of)

2015-01-15

Highlights: • Synthesis of Fe doped In{sub 2}O{sub 3} powders using a solid state reaction. • Characterization of the samples using XRD, UV–vis-NIR, FT-IR, and VSM. • All Fe doped In{sub 2}O{sub 3} powders exhibited the cubic structure of In{sub 2}O{sub 3}. • All the Fe doped In{sub 2}O{sub 3} samples exhibited room temperature ferromagnetism. - Abstract: Iron doped indium oxide dilute magnetic semiconductor (In{sub 1−x}Fe{sub x}){sub 2}O{sub 3} (x = 0.00, 0.03, 0.05, and 0.07) powders were synthesized by standard solid state reaction method followed by vacuum annealing. The effect of Fe concentration on structural, optical, and magnetic properties of the (In{sub 1−x}Fe{sub x}){sub 2}O{sub 3} powders have been systematically studied. X-ray diffraction patterns confirmed the polycrystalline cubic structure of all the samples. An optical band gap increases from 3.12 eV to 3.16 eV while Fe concentration varying from 0.03 to 0.07. Magnetic studies reveal that virgin/undoped In{sub 2}O{sub 3} is diamagnetic. However, all the Fe-doped In{sub 2}O{sub 3} samples are ferromagnetic. The saturation magnetization (M{sub s}) of ferromagnetic (In{sub 1−x}Fe{sub x}){sub 2}O{sub 3} (x = 0.03, 0.05, and 0.07) samples increases from 11.56 memu/g to 148.64 memu/g with x = 0.03–0.07. The observed ferromagnetism in these samples was attributed to magnetic nature of the dopant (Fe) as well as defects created in the samples during vacuum annealing.

Tri-functional Fe2O3-encased Ag-doped ZnO nanoframework: magnetically retrievable antimicrobial photocatalyst

Science.gov (United States)

Karunakaran, Chockalingam; Vinayagamoorthy, Pazhamalai

2016-11-01

Fe2O3-encased ZnO nanoframework was obtained by hydrothermal method and was doped with Ag through photoreduction process. Energy dispersive x-ray spectroscopy, transmission electron microscopy (TEM), high resolution TEM, selected area electron diffractometry, x-ray diffractometry and Raman spectroscopy were employed for the structural characterization of the synthesized material. While the charge transfer resistance of the prepared nanomaterial is larger than those of Fe2O3 and ZnO the coercivity of the nanocomposite is less than that of hydrothermally obtained Fe2O3 nanostructures. Although Fe2O3/Ag-ZnO exhibits weak visible light absorption its band gap energy does not differ from that of ZnO. The photoluminescence of the fabricated nanoframework is similar to that of ZnO. The radiative recombination of charge carriers is slightly slower in Fe2O3/Ag-ZnO than in ZnO. The synthesized Fe2O3-encased Ag-doped ZnO, under UV A light, exhibits sustainable photocatalytic activity to degrade dye and is magnetically recoverable. Also, the Fe2O3/Ag-ZnO nanocomposite disinfects bacteria effectively in absence of direct illumination.

Photoelectrochemical Characterization of Sprayed α-Fe2O3 Thin Films: Influence of Si Doping and SnO2 Interfacial Layer

Directory of Open Access Journals (Sweden)

Yongqi Liang

2008-01-01

Full Text Available α-Fe2O3 thin film photoanodes for solar water splitting were prepared by spray pyrolysis of Fe(AcAc3. The donor density in the Fe2O3 films could be tuned between 1017–1020 cm-3 by doping with silicon. By depositing a 5 nm SnO2 interfacial layer between the Fe2O3 films and the transparent conducting substrates, both the reproducibility and the photocurrent can be enhanced. The effects of Si doping and the presence of the SnO2 interfacial layer were systematically studied. The highest photoresponse is obtained for Fe2O3 doped with 0.2% Si, resulting in a photocurrent of 0.37 mA/cm2 at 1.23 VRHE in a 1.0 M KOH solution under 80 mW/cm2 AM1.5 illumination.

Comparative study of (N, Fe) doped TiO{sub 2} photocatalysts

Energy Technology Data Exchange (ETDEWEB)

Larumbe, S., E-mail: silvia.larumbe@unavarra.es [Departamento Física, Universidad Pública de Navarra, Campus de Arrosadia, 31006 Pamplona (Spain); Monge, M. [Departamento de Química, Universidad de la Rioja, Centro de Investigación en Síntesis Química (CISQ), Complejo Científico Tecnológico, 26006 Logroño (Spain); Gómez-Polo, C. [Departamento Física, Universidad Pública de Navarra, Campus de Arrosadia, 31006 Pamplona (Spain)

2015-02-01

Highlights: • Fe, N doped TiO{sub 2} nanoparticles were synthesized by sol–gel. • The nitrogen content controlled the mean size of nanoparticles and afterwards the modification of cell parameters with respect the undoped sample. • Both doping elements induced the increase of the anatase-rutile transition temperature. • A red-shift is observed in the absorption spectra with the introduction of both elements. • An improvement of photocatalytic activity is observed with the introduction of nitrogen under UV and Visible light. However for higher concentrations a decrease in kinetic constants was observed as consequence of the oxygen vacancies acting as recombination centers. On the contrary, a deterioration of photocatalytic efficiency is found for the Fe doped samples. • A correlation between magnetic behavior and photocatalytic activity was found. - Abstract: The effect of N and Fe doping on the structural, optical, photocatalytic and magnetic properties of TiO{sub 2} nanoparticles is analyzed. Undoped, N and Fe doped TiO{sub 2} nanoparticles were synthesized by sol–gel method. Titanium tetraisopropoxide (TTIP) was used as the alkoxyde precursor and iron (III) nitrate and urea were the employed precursors to obtain Fe and N doped TiO{sub 2} nanoparticles, respectively. Differential Scanning Calorimetry (DSC) and Thermogravimetrical Analysis (TGA) enabled the analysis of the thermal decomposition process and the final calcination temperature. X-Ray Diffraction patterns of the calcined nanoparticles displayed a monophasic anatase structure in all the samples with mean crystallite diameter around 4–6 nm. The introduction of Fe or N induced a red-shift in the absorption spectra. Such a red-shift is characterized by a decrease in the band-gap energy and the occurrence of an absorption (Urbach) tail in the visible region. Finally, the photocatalytic efficiency was evaluated under UV and Visible light, obtaining an improvement of the kinetic constants in

Superparamagnetic behavior of Fe-doped SnO2 nanoparticles

International Nuclear Information System (INIS)

Hachisu, M.; Onuma, K.; Kondo, T.; Miike, K.; Miyasaka, T.; Mori, K.; Ichiyanagi, Y.

2014-01-01

SnO 2 is an n-type semiconductor with a wide band gap of 3.62 eV, and SnO 2 nanoparticles doped with magnetic ions are expected to realized new diluted magnetic semiconductors (DMSs). Realizing ferromagnetism at room temperature is important for spintronics device applications, and it is interesting that the magnetic properties of these DMS systems can be varied significantly by modifying the preparation methods or conditions. In this study, the magnetic properties of Fe-doped (3% and 5%) SnO 2 nanoparticles, prepared using our novel chemical preparation method and encapsulated in amorphous SiO 2 , were investigated. The particle size (1.8–16.9 nm) and crystal phase were controlled by the annealing temperature. X-ray diffraction confirmed a rutile SnO 2 single-phase structure for samples annealed at 1073–1373 K, and the composition was confirmed using X-ray fluorescence analysis. SQUID magnetometer measurements revealed superparamagnetic behavior of the 5%-Fe-doped sample at room temperature, although SnO 2 is known to be diamagnetic. Magnetization curves at 5 K indicated that the 3%-Fe-doped has a larger magnetization than that of the 5%-Fe-doped sample. We conclude that the magnetization of the 5%-Fe-doped sample decreased at 5 K due to the superexchange interaction between the antiferromagnetic coupling in the nanoparticle system

Superparamagnetic behavior of Fe-doped SnO2 nanoparticles

Science.gov (United States)

Hachisu, M.; Onuma, K.; Kondo, T.; Miike, K.; Miyasaka, T.; Mori, K.; Ichiyanagi, Y.

2014-02-01

SnO2 is an n-type semiconductor with a wide band gap of 3.62 eV, and SnO2 nanoparticles doped with magnetic ions are expected to realized new diluted magnetic semiconductors (DMSs). Realizing ferromagnetism at room temperature is important for spintronics device applications, and it is interesting that the magnetic properties of these DMS systems can be varied significantly by modifying the preparation methods or conditions. In this study, the magnetic properties of Fe-doped (3% and 5%) SnO2 nanoparticles, prepared using our novel chemical preparation method and encapsulated in amorphous SiO2, were investigated. The particle size (1.8-16.9 nm) and crystal phase were controlled by the annealing temperature. X-ray diffraction confirmed a rutile SnO2 single-phase structure for samples annealed at 1073-1373 K, and the composition was confirmed using X-ray fluorescence analysis. SQUID magnetometer measurements revealed superparamagnetic behavior of the 5%-Fe-doped sample at room temperature, although SnO2 is known to be diamagnetic. Magnetization curves at 5 K indicated that the 3%-Fe-doped has a larger magnetization than that of the 5%-Fe-doped sample. We conclude that the magnetization of the 5%-Fe-doped sample decreased at 5 K due to the superexchange interaction between the antiferromagnetic coupling in the nanoparticle system.

Room temperature ferromagnetism in Fe-doped CeO2 nanoparticles.

Science.gov (United States)

Maensiri, Santi; Phokha, Sumalin; Laokul, Paveena; Seraphin, Supapan

2009-11-01

RT ferromagnetism was observed in nanoparticles of Fe-doped CeO2 (i.e., Ce(0.97)Fe(0.03)O2) synthesized by a sol-gel method. The undoped and Fe-doped CeO2 were characterized by XRD, Raman spectroscopy, TEM, and VSM. The undoped samples and Ce(0.97)Fe(0.03)O2 precursor exhibit a diamagnetic behavior. The 673 K-calcined Ce(0.97)Fe(0.03)O2 sample is paramagnetic whereas 773 and 873 K-calcined Ce(0.97)Fe(0.03)O2 samples are ferromagnetism having the magnetizations of 4.65 x 10(-3) emu/g and 6.20 x 10(-3) emu/g at 10 kOe, respectively. Our results indicate that the ferromagnetic property is intrinsic to the Fe-doped CeO2 system and is not a result of any secondary magnetic phase or cluster formation.

Synthesis, characterization and magnetic property of maghemite (γ-Fe{sub 2}O{sub 3}) nanoparticles and their protective coating with pepsin for bio-functionalization

Energy Technology Data Exchange (ETDEWEB)

Bandhu, A.; Sutradhar, S.; Mukherjee, S. [Solid State Research Laboratory, Department of Physics, Burdwan University, Burdwan 713104, West Bengal (India); Greneche, J.M. [Laboratoire de Physique de l’Etat Condensé – UMR CNRS 6087, Université du Maine, 72085, Le Mans Cedex 9 (France); Chakrabarti, P.K., E-mail: pabitra_c@hotmail.com [Solid State Research Laboratory, Department of Physics, Burdwan University, Burdwan 713104, West Bengal (India)

2015-10-15

Highlights: • Maghemite nanoparticles were prepared by a modified co-precipitation method. • Nanoparticles were then successfully coated with pepsin for bio-functionlization. • XRD and Mössbauer spectra confirmed the maghemite phase of the nanoparticles. • Magnetic data were analysed to evaluate particle size, anisotropy etc. - Abstract: Maghemite nanoparticles (γ-Fe{sub 2}O{sub 3}) are prepared by co-precipitation method. To obtain bio-functionalized magnetic nanoparticles for magnetically controlled drug delivery, the prepared nanoparticles are successfully coated with pepsin, a bio-compatible polymer and digestive enzyme. Crystallographic phase of the nanoparticles is confirmed by X-ray diffractograms (XRD), high resolution transmission electron microscopy (HRTEM) and {sup 57}Fe Mössbauer spectrometry. The average size of nanoparticles/nanocrystallites is estimated from the (3 1 1) peak of the XRD pattern using Debye–Scherrer formula. Results of HRTEM of coated and bare samples are in good agreement with those extracted from the XRD analysis. The dynamic magnetic properties are observed and different quantities viz., coercive field, magnetization, remanence, hysteresis losses etc., are estimated, which confirmed the presence of superparamagnetic relaxation of nanoparticles. Mössbauer spectra of the samples recorded at both 300 and 77 K, confirmed that the majority of particles are maghemite together with a very small fraction of magnetite nanoparticles.

Superparamagnetic behavior of Fe-doped SnO{sub 2} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Hachisu, M.; Onuma, K.; Kondo, T.; Miike, K.; Miyasaka, T.; Mori, K.; Ichiyanagi, Y. [Department of Physics, Graduate School of Engineering, Yokohama National University, 79-5 Tokiwadai, Hodogaya, Yokohama, Kanagawa 240-8501 (Japan)

2014-02-20

SnO{sub 2} is an n-type semiconductor with a wide band gap of 3.62 eV, and SnO{sub 2} nanoparticles doped with magnetic ions are expected to realized new diluted magnetic semiconductors (DMSs). Realizing ferromagnetism at room temperature is important for spintronics device applications, and it is interesting that the magnetic properties of these DMS systems can be varied significantly by modifying the preparation methods or conditions. In this study, the magnetic properties of Fe-doped (3% and 5%) SnO{sub 2} nanoparticles, prepared using our novel chemical preparation method and encapsulated in amorphous SiO{sub 2}, were investigated. The particle size (1.8–16.9 nm) and crystal phase were controlled by the annealing temperature. X-ray diffraction confirmed a rutile SnO{sub 2} single-phase structure for samples annealed at 1073–1373 K, and the composition was confirmed using X-ray fluorescence analysis. SQUID magnetometer measurements revealed superparamagnetic behavior of the 5%-Fe-doped sample at room temperature, although SnO{sub 2} is known to be diamagnetic. Magnetization curves at 5 K indicated that the 3%-Fe-doped has a larger magnetization than that of the 5%-Fe-doped sample. We conclude that the magnetization of the 5%-Fe-doped sample decreased at 5 K due to the superexchange interaction between the antiferromagnetic coupling in the nanoparticle system.

Thermal decomposition study of Mn doped Fe3O4 nanoparticles

Science.gov (United States)

Malek, Tasmira J.; Chaki, S. H.; Tailor, J. P.; Deshpande, M. P.

2016-05-01

Fe3O4 is an excellent magnetic material among iron oxides. It has a cubic inverse spinel structure exhibiting distinguished electric and magnetic properties. In this paper the authors report the synthesis of Mn doped Fe3O4 nanoparticles by wet chemical reduction technique at ambient temperature and its thermal characterization. Ferric chloride hexa-hydrate (FeCl3•6H2O), manganese chloride tetra-hydrate (MnCl2•4H2O) and sodium boro-hydrate (NaBH4) were used for synthesis of Fe3O4 nanoparticles at ambient temperature. The elemental composition of the as-synthesized Mn doped Fe3O4 nanoparticles were determined by energy dispersive analysis of X-rays (EDAX) technique. Thermogravimetric (TG) and differential thermal analysis (DTA) were carried out on the Mn doped Fe3O4 nanoparticles in the temperature range of ambient to 1124 K. The thermo-curves revealed that the particles decompose by four steps. The kinetic parameters were evaluated using non-mechanistic equations for the thermal decomposition.

Spin Seebeck effect in insulating epitaxial γ−Fe2O3 thin films

Directory of Open Access Journals (Sweden)

P. Jiménez-Cavero

2017-02-01

Full Text Available We report the fabrication of high crystal quality epitaxial thin films of maghemite (γ−Fe2O3, a classic ferrimagnetic insulating iron oxide. Spin Seebeck effect (SSE measurements in γ−Fe2O3/Pt bilayers as a function of sample preparation conditions and temperature yield a SSE coefficient of 0.5(1 μV/K at room temperature. Dependence on temperature allows us to estimate the magnon diffusion length in maghemite to be in the range of tens of nanometers, in good agreement with that of conducting iron oxide magnetite (Fe3O4, establishing the relevance of spin currents of magnonic origin in magnetic iron oxides.

Photoelectrochemical Characterization of Sprayed alpha-Fe2O3 Thin Films : Influence of Si Doping and SnO2 Interfacial Layer

NARCIS (Netherlands)

Liang, Y.; Enache, C.S.; Van De Krol, R.

2008-01-01

a-Fe2O3 thin film photoanodes for solar water splitting were prepared by spray pyrolysis of Fe(AcAc)3. The donor density in the Fe2O3 films could be tuned between 10171020cm-3 by doping with silicon. By depositing a 5 nm SnO2 interfacial layer between the Fe2O3 films and the transparent conducting

Synthesis and properties of iridium-doped hematite ({alpha}-Fe{sub 2}O{sub 3})

Energy Technology Data Exchange (ETDEWEB)

Krehula, Stjepko, E-mail: krehul@irb.hr [Division of Materials Chemistry, Ruder Boskovic Institute, P.O. Box 180, HR-10002 Zagreb (Croatia); Stefanic, Goran [Division of Materials Chemistry, Ruder Boskovic Institute, P.O. Box 180, HR-10002 Zagreb (Croatia); Zadro, Kreso [Department of Physics, Faculty of Science, University of Zagreb, Bijenicka 32, 10000 Zagreb (Croatia); Kratofil Krehula, Ljerka [Faculty of Chemical Engineering and Technology, University of Zagreb, Marulicev trg 19, 10000 Zagreb (Croatia); Marcius, Marijan; Music, Svetozar [Division of Materials Chemistry, Ruder Boskovic Institute, P.O. Box 180, HR-10002 Zagreb (Croatia)

2012-12-25

Highlights: Black-Right-Pointing-Pointer Ir-doped hematites were prepared by heating Ir-doped goethites. Black-Right-Pointing-Pointer Ir-doping in hematite led to an increase in unit cell and a decrease in crystallite size. Black-Right-Pointing-Pointer Ir-doping significantly affected magnetic, infrared and UV-Vis properties of hematite. Black-Right-Pointing-Pointer The Morin transition temperature increased with an increase in Ir-doping. Black-Right-Pointing-Pointer Ir ions brought about changes in the size and shape of the formed hematite particles. - Abstract: The effect of the incorporation of Ir{sup 3+} ions on the properties of {alpha}-Fe{sub 2}O{sub 3} formed by dehydroxylation of {alpha}-FeOOH was investigated using X-ray powder diffraction (XRD), thermogravimetric analysis (TGA), {sup 57}Fe Moessbauer, UV-Vis-NIR and FT-IR spectroscopies, SQUID magnetometer, field emission scanning electron microscopy (FE-SEM) and energy dispersive X-ray spectroscopy (EDS). Pure and Ir-doped hematite samples were obtained by heating of pure and Ir-doped goethites ({alpha}-FeOOH) formed by precipitation from mixed Fe(III)-Ir(III) chloride solutions in a highly alkaline medium. The incorporation of Ir{sup 3+} ions into the {alpha}-Fe{sub 2}O{sub 3} structure led to changes in unit-cell dimensions, crystallinity, particle size and shape, as well as changes in the magnetic, infrared and UV-Vis properties. An increase in the temperature of the Morin transition with an increase in Ir-doping was observed by Moessbauer spectroscopy and magnetic measurements.

Study on the water durability of zinc boro-phosphate glasses doped with MgO, Fe2O3, and TiO2

Science.gov (United States)

Hwang, Moon Kyung; Ryu, Bong Ki

2016-07-01

The water durability of zinc boro-phosphate (PZB) glasses with the composition 60P2O5-20ZnO-20B2O3- xMeO ( x = 0, 2, 4, 6 and MeO = MgO, Fe2O3, or TiO2) (mol%) was measured, and PZB glass was studied in terms of its thermal properties, density, and FTIR characteristics. The surface conditions and corrosion byproducts were analyzed using scanning electron microscopy. When MgO, Fe2O3, and TiO2 were doped into the PZB glass, Q2 was decreased and Q1 was increased in the phosphate structure, while the number of BO4 structures increased with increasing MeO content. The density of the PZB glass was increased by the addition of Fe2O3 and TiO2, while the glass transition temperature ( T g ) and dilatometric softening temperature ( T d ) were increased when additional MgO, Fe2O3, and TiO2 were added. From the weight loss analysis (95 ◦ C, 96 h), TiO2 doped glass showed the lowest weight loss (1.70 × 10 -3 g/cm2) while MgO doped glass showed the highest value (2.44 × 10 -3 g/cm2), compared with PZB glass (3.07 × 10 -3 g/cm2). These results were discussed in terms of the Me n+ ions in the glass structure, and their different coordination numbers and bonding strengths.

Structure and magnetic properties of Fe doped In{sub 2}O{sub 3} thin films prepared by electron beam evaporation

Energy Technology Data Exchange (ETDEWEB)

Krishna, N. Sai; Kaleemulla, S., E-mail: skaleemulla@gmail.com; Rao, N. Madhusudhana; Krishnamoorthi, C.; Begam, M. Rigana [Thin Films Laboratory, School of Advanced Sciences, VIT University, Vellore – 632014 (India); Amarendra, G. [Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam – 603102 (India); UGC-DAE-CSR, Kalpakkam Node, Kokilamedu, Tamilnadu -603104 (India)

2015-06-24

Pure and Fe (7 at.%) doped In{sub 2}O{sub 3} thin films were grown onto the glass substrates by electron beam evaporation technique. The structural and magnetic properties of the pure and Fe doped In{sub 2}O{sub 3} thin films have been studied. The undoped and Fe doped In{sub 2}O{sub 3} thin films shown ferromagnetic property at room temperature. A magnetization of 24 emu/cm{sup 3} was observed for pure In{sub 2}O{sub 3} thin films. The magnetization of 38.23 emu/cm{sup 3} was observed for the Fe (7 at.%) doped In{sub 2}O{sub 3} thin films.

Synthesis and microwave absorption enhancement of Fe-doped NiO@SiO2@graphene nanocomposites

International Nuclear Information System (INIS)

Wang, Lei; Huang, Ying; Ding, Xiao; Liu, Panbo; Zong, Meng; Wang, Yan

2013-01-01

Highlights: • Fe-doped NiO@SiO 2 @graphene composites have excellent microwave performance. • The reflection loss of Fe doped NiO@SiO 2 @graphene was below −10 dB in 7–11 GHz. • The maximum absorption of Fe-doped NiO@SiO 2 @graphene was −51.2 dB at 8.6 GHz. -- Abstract: Fe-doped NiO@SiO 2 @graphene nanocomposites have been successfully fabricated for the first time, in which Fe-doped NiO nanoparticles are about 3 nm in diameter. In order to measure their electromagnetic properties, Fe-doped NiO@SiO 2 @graphene (25 wt%) wax composites were then prepared. The experimental results show that Fe-doped NiO@SiO 2 @graphene nanocomposites exhibit significantly enhanced microwave absorption performance in terms of both the maximum reflection loss value and the absorption bandwidth in comparison with NiO@SiO 2 @graphene. The maximum reflection loss of Fe-doped NiO@SiO 2 @graphene nanocomposites can reach −51.2 dB at 8.6 GHz with a thickness of 4 mm, and the absorption bandwidth with the reflection loss below −10 dB is 4 GHz (from 7 to 11 GHz). Therefore, this kind of nanocomposites may have the potential as high-efficient absorbers for microwave absorption applications

N-TiO2/gamma-Al2O3 granules: preparation, characterization and photocatalytic activity for the degradation of 2,4-dichlorophenol.

Science.gov (United States)

Huang, Donggen; Xie, Wenfa; Tu, Zhibin; Zhang, Feng; Quan, Shuiqing; Liu, Lei

2013-01-01

Nitrogen doping TiO2 and gamma-Al2O3 composite oxide granules (N-TiO2/gamma-Al2O3) were prepared by co-precipitation/oil-drop/calcination in gaseous NH3 process using titanium sulphate and aluminum nitrate as raw materials. After calcination at 550 degrees C in NH3 atmosphere, the composite granules showed anatase TiO2 and gamma-Al2O3 phases with the granularity of 0.5-1.0 mm. The anatase crystallite size of composite granules was range from 3.5-25 nm calculated from XRD result. The UV-Vis spectra and N 1s XPS spectra indicated that N atoms were incorporated into the TiO2 crystal lattice. The product granules could be used as a photocatalyst in moving bed reactor, and was demonstrated a higher visible-light photocatalytic activity for 2,4-dichlorophenol degradation compared with commercial P25 TiO2. When the mole ratio of TiO2 to Al2O3 equal to 1.0 showed the highest catalytic activity, the degradation percentage of 2,4-chlorophenol could be up to 92.5%, under 60 W fluorescent light irradiation for 9 hours. The high visible-light photocatalytic activity might be a synergetic effect of nitrogen doping and the form of binary metal oxide of TiO2 and gamma-Al2O3.

Synthesis, characterization and gas sensing properties of undoped and Zn-doped γ-Fe2O3-based gas sensors

International Nuclear Information System (INIS)

Jing Zhihong

2006-01-01

In this study, undoped and Zn-doped γ-Fe 2 O 3 nanopowders have been prepared using Fe(NO 3 ) 3 .9H 2 O and Zn(NO 3 ) 2 .6H 2 O as starting materials and lauryl alcohol as anhydrous medium. Thermo-gravimetric analysis (TGA), differential thermal analysis (DTA), X-ray diffraction (XRD) and transmission electron micrograph (TEM) were employed to characterize the products. Sensitivity characteristics of the undoped and Zn-doped γ-Fe 2 O 3 semiconductor gas sensors have been investigated. The results show that both of the undoped and 15 mol% Zn-doped γ-Fe 2 O 3 -based gas sensors present good sensitivity and selectivity to acetone and ethanol in presence of CH 4 , H 2 and CO at the operating temperatures of 240 and 270 deg. C, respectively. After being doped with 15 mol% Zn addition, the γ-Fe 2 O 3 -based gas element displays higher sensitivity and selectivity as well as shorter response-recovery time compared with the undoped, suggesting that the promoting effect of ZnO is excellent. So, it seems that the γ-Fe 2 O 3 -based gas sensor doped with 15 mol% Zn is expected to be a promising sensor for detecting acetone and ethanol

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.

SYNTHESIS OF M–Nd DOPED Fe3O4 NANOPARTICLES (M = Co ...

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nanoparticles were spherical shaped with inverse spinel structure. ... To obtain nano sized spinel ferrite particles, various preparation techniques have been ... SEM images of (a) Fe3O4, (b) Fe3O4 doped with Nd3+ and Co2+, (c) Fe3O4 doped with. Nd3+ .... Nayar, S.; Mir, A.; Ashok, A.; Sharma, A. J. Bionic Eng. 2010, 7, 29.

Effect of Li2O-doping of nanocrystalline CoO/Fe2O3 on isopropanol conversion

International Nuclear Information System (INIS)

El-Shobaky, Hala G.; Ali, Suzan A.H.; Hassan, Neven A.

2007-01-01

The catalytic conversion of isopropanol was carried out over pure and Li 2 O-doped (0.75-4.5 mol%) cobalt ferrite prepared by heating Fe/Co mixed hydroxides at 400 and 600 deg. C. The techniques employed were XRD, N 2 adsorption at -196 deg. C and conversion of isopropanol at 200-400 deg. C using a flow method. The results showed that Li 2 O-doping and increasing the heating temperature of the system investigated from 400 to 600 deg. C stimulated CoFe 2 O 4 formation also. Pure and variously doped solids were moderately crystallized CoFe 2 O 4 phase having a crystallite size varying between 5 and 15 nm. The S BET of various solids was found to decrease by increasing their calcination temperature and also by doping with 4.5 mol% Li 2 O. However, this treatment, resulted in a significant increase in their catalytic activities which much increased by doping. The presence of 1.5 mol% Li 2 O brought about an increase in the catalytic activity, measured at 300 deg. C, of 97% and 63% for the solids being calcined at 400 and 600 deg. C, respectively. All solids investigated behaved as dehydrogenation catalysts (having selectivities to acetone formation above 95%). The doping process did not alter the mechanism of dehydrogenation of isopropanol, but increased the concentration of active sites involved in the catalyzed reaction

Doped titanium dioxide nanocrystalline powders with high photocatalytic activity

International Nuclear Information System (INIS)

Castro, A.L.; Nunes, M.R.; Carvalho, M.D.; Ferreira, L.P.; Jumas, J.-C.; Costa, F.M.; Florencio, M.H.

2009-01-01

Doped titanium dioxide nanopowders (M:TiO 2 ; M=Fe, Co, Nb, Sb) with anatase structure were successfully synthesized through an hydrothermal route preceded by a precipitation doping step. Structural and morphological characterizations were performed by powder XRD and TEM. Thermodynamic stability studies allowed to conclude that the anatase structure is highly stable for all doped TiO 2 prepared compounds. The photocatalytic efficiency of the synthesized nanopowders was tested and the results showed an appreciable enhancement in the photoactivity of the Sb:TiO 2 and Nb:TiO 2 , whereas no photocatalytic activity was detected for the Fe:TiO 2 and Co:TiO 2 nanopowders. These results were correlated to the doping ions oxidation states, determined by Moessbauer spectroscopy and magnetization data. - Graphical abstract: Doped titanium dioxide nanopowders (M:TiO 2 ; M=Fe, Co, Nb, Sb) with highly stable anatase structure were successfully synthesized through an hydrothermal route. The photocatalytic efficiencies of the synthesized nanopowders were tested and the results show an appreciable enhancement in the photoactivity of the Sb:TiO 2 and Nb:TiO 2 .

Influences of the iron ion (Fe3+)-doping on structural and optical properties of nanocrystalline TiO2 thin films prepared by sol-gel spin coating

International Nuclear Information System (INIS)

Ben Naceur, J.; Mechiakh, R.; Bousbih, F.; Chtourou, R.

2011-01-01

Titanium dioxide (TiO 2 ) thin films doping of various iron ion (Fe 3+ ) concentrations were deposited on silicon (Si) (100) and quartz substrates by sol-gel Spin Coating technique followed by a thermal treatment at 600 deg. C. The structure, surface morphology and optical properties, as a function of the doping, have been studied by X-ray diffractometer (XRD), Raman, ultraviolet-visible (UV-vis) and Spectroscopic Ellipsometry (SE). XRD and Raman analyzes of our thin films show that the crystalline phase of TiO 2 thin films comprised only the anatase TiO 2 , but the crystallinity decreased when the Fe 3+ content increased from 0% to 20%. During the Fe 3+ addition to 20%, the phase of TiO 2 thin film still maintained the amorphous state. The grain size calculated from XRD patterns varies from 29.3 to 22.6 nm. The complex index and the optical band gap (E g ) of the films were determined by the spectroscopic ellipsometry analysis. We have found that the optical band gap decreased with an increasing Fe 3+ content.

Fe/Fe3C decorated 3-D porous nitrogen-doped graphene as a cathode material for rechargeable Li–O2 batteries

International Nuclear Information System (INIS)

Lai, Yanqing; Chen, Wei; Zhang, Zhian; Qu, Yaohui; Gan, Yongqing; Li, Jie

2016-01-01

Graphical abstract: Fe/Fe 3 C decorated 3-D porous N-doped graphene are prepaed by a one-step carbonization process, with MOF as the structure-directing agent. The method provides a simple and scalable route for preparing 3-D porous graphene materials.The as-prepared material possesses an excellent bi-functional electrocatalytic activity. While applied as the cathode materials of Li–O 2 batteries, the cell exihibits high capacity and considerable rate capability. - Highlights: • A facile simple strategy is employed to in-situ fabricate Fe/Fe 3 C decorated 3-D porous nitrogen-doped graphene. • MIL-100(Fe), a kind of metal-organic framework, is proved playing a structure-directing role in this advanced synthesis route. • This material possesses excellent bi-functional electro-catalytic activity for ORR and OER and shows good electrochemical performance while used as cathode material for Li–O 2 batteries. • The MOF-assisted synthesis method would be a promising new strategy for the synthesis of 3-D porous graphene materials. - Abstract: Fe/Fe 3 C decorated 3-D porous N-doped graphene (F-PNG) is designed and synthesized via a one-step carbonization route. During the process, MIL-100(Fe), a kind of metal organic frameworks (MOFs) plays a structure-directing role. It is found that F-PNG with 3-D porous structure is constituted by N-doped graphene and extremely small Fe/Fe 3 C particles uniformly distribute on the surface of graphene. This rationally designed F-PNG possesses excellent oxygen reduction reaction and oxygen evolution reaction bifunctional electrocatalytic activity. While the material is explored as a cathode of Li–O 2 batteries, it exhibits excellent electrochemical performances, delivering a discharge voltage platform of ∼2.91 V and a charge voltage platform of ∼3.52 V at 0.1 mA cm −2 , showing a good cycle performance and having a discharge capacity of ∼7150 mAh g −1 carbon+catalyst at 0.1 mA cm −2 . The excellent performance of

Identification of ε-Fe{sub 2}O{sub 3} nano-phase in borate glasses doped with Fe and Gd

Energy Technology Data Exchange (ETDEWEB)

Ivanova, O.S.; Ivantsov, R.D. [L.V. Kirensky Institute of Physics, Siberian Branch of RAS, 660036 Krasnoyarsk (Russian Federation); Edelman, I.S., E-mail: ise@iph.krasn.ru [L.V. Kirensky Institute of Physics, Siberian Branch of RAS, 660036 Krasnoyarsk (Russian Federation); Petrakovskaja, E.A. [L.V. Kirensky Institute of Physics, Siberian Branch of RAS, 660036 Krasnoyarsk (Russian Federation); Velikanov, D.A. [L.V. Kirensky Institute of Physics, Siberian Branch of RAS, 660036 Krasnoyarsk (Russian Federation); Siberian Federal University, 660036 Krasnoyarsk (Russian Federation); Zubavichus, Y.V. [NRC “Kurchatov Institute”, 123182 Moscow (Russian Federation); Zaikovskii, V.I. [Boreskov Institute of Catalysis, Siberian Branch of RAS, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, 630090 Novosibirsk (Russian Federation); Stepanov, S.A. [Vavilov State Optical Institute, All-Russia Research Center, 192371 Petersburg (Russian Federation)

2016-03-01

A new type of magnetic nanoparticles was revealed in borate glasses co-doped with low contents of iron and gadolinium. Structure and magnetic properties of the particles differ essentially from that of the α-Fe{sub 2}O{sub 3}, γ-Fe{sub 2}O{sub 3}, or Fe{sub 3}O{sub 4} nanoparticles which were detected earlier in similar glass matrices. Transmission electron microscopy including STEM-HAADF and EDX, synchrotron radiation-based XRD, static magnetic measurements, magnetic circular dichroism, and electron magnetic resonance studies allow referring the nanoparticles to the iron oxide phase-ε-Fe{sub 2}O{sub 3}. Analysis of the data set has shown that it is Gd atoms that govern the process of nanoparticles’ nucleation and its incorporation into the particles in different proportions can be used to adjust their magnetic and magneto-optical characteristics. - Highlights: • Alumina-potassium-borate glasses co-doped with Fe and Gd are studied. • Magnetic nanoparticles with structure close to ε-Fe{sub 2}O{sub 3} are shown to arise in glasses • Magnetic hysteresis loops and EMR evidence on the ferromagnetic and paramagnetic nano-phases coexistence. • Magnetic circular dichroism for ε-Fe{sub 2}O{sub 3} is studied for the first time.

Structural and magnetic studies of tin doped α-Fe{sub 2}O{sub 3} (α-Sn{sub x}Fe{sub 2-x}O{sub 3}) nanoparticles prepared by microwave assisted synthesis

Energy Technology Data Exchange (ETDEWEB)

Bindu, K.; Nagaraja, H. S., E-mail: hosakoppa@gmail.com [Material Research Laboratory, Department of Physics, National Institute of Technology Karnataka, Surathkal, Srinivasnagar, Mangalore-575 025, Karnataka (India); Chowdhury, P. [Nanomaterials Research Laboratory, Surface Engineering Division, National Aerospace Laboratories, Council of Scientific and Industrial Research, Bangalore-560 017, Karnataka (India); Ajith, K. M. [Computational Physics Laboratory, Department of Physics, National Institute of Technology Karnataka, Surathkal, Srinivasnagar, Mangalore-575 025, Karnataka (India)

2016-05-06

Hematite (α-Fe{sub 2}O{sub 3}) doped with tetravalent ions have potential applications in various fields such as gas sensors, memories, energy storage devices because of their electrical and magnetic properties. Microwave assisted synthesis was used to prepare Tin doped α-Fe{sub 2}O{sub 3} [α-Sn{sub x}Fe{sub 2-x}O{sub 3}]. The structural and morphological studies were investigated using X-ray diffraction (XRD) and Scanning electron microscopy (SEM). XRD patterns revealed that α-Fe{sub 2}O{sub 3} and α-Sn{sub x}Fe{sub 2-x}O{sub 3} were having rhombohedral structure. The compositional study was done by Energy dispersive X-ray Spectroscopy (EDS). The magnetic properties were studied by Vibrating Sample Magnetometry (VSM). Results shows that the prepared samples were found to be antiferromagnetic in nature and the results are discussed in detail.

The Formation of Lithiated Ti-Doped α-Fe2O3 Nanocrystalline Particles by Mechanical Milling of Ti-Doped Lithium Spinel Ferrite

International Nuclear Information System (INIS)

Widatallah, H. M.; Gismelseed, A. M.; Bouziane, K.; Berry, F. J.; Al Rawas, A. D.; Al-Omari, I. A.; Yousif, A. A.; Elzain, M. E.

2004-01-01

The milling of spinel-related Ti-doped Li 0.5 Fe 2.5 O 4 for different times is studied with XRD, Moessbauer spectroscopy and magnetic measurements. Milling converts the material to Li-Ti-doped α-Fe 2 O 3 nanocrystalline particles via an intermediate γ-LiFeO 2 -related phase. The role played by the dopant Ti-ion in the process is emphasized.

Synthesis of Nano-Ilmenite (FeTiO3) doped TiO2/Ti Electrode for Photoelectrocatalytic System

Science.gov (United States)

Hikmawati; Watoni, A. H.; Wibowo, D.; Maulidiyah; Nurdin, M.

2017-11-01

Ilmenite (FeTiO3) doped on Ti and TiO2/Ti electrodes were successfully prepared by using the sol-gel method. The structure, morphology, and optical properties of FeTiO3 are characterized by XRD, UV-Vis DRS, and SEM. The FeTiO3 and TiO2 greatly affect the photoelectrocatalysis performance characterized by Linear Sweep Voltammetry (LSV) and Cyclic Voltammetry (CV). The characterization result shows a band gap of FeTiO3 is 2.94 eV. XRD data showed that FeTiO3 formed at 2θ were 35.1° (110), 49.9° (024), and 61.2° (214). The morphology of FeTiO3/Ti and FeTiO3.TiO2/Ti using SEM shows that the formation of FeTiO3 thin layer signifies the Liquid Phase Deposition method effectively in the coating process. Photoelectrochemical (PEC) test showed that FeTiO3.TiO2/Ti electrode was highly oxidation responsive under visible light compared to the FeTiO3/Ti electrodes i.e. 7.87×10-4 A and 9.87×10-5 A. Degradation test of FeTiO3/Ti and FeTiO3.TiO2/Ti electrodes on titan yellow showed that the percentages of degradation with photoelectrocatalysis at 0.5 mg/L were 41% and 43%, respectively.

Surface spins disorder in uncoated and SiO2 coated maghemite nanoparticles

International Nuclear Information System (INIS)

Zeb, F.; Nadeem, K.; Shah, S. Kamran Ali; Kamran, M.; Gul, I. Hussain; Ali, L.

2017-01-01

We studied the surface spins disorder in uncoated and silica (SiO 2 ) coated maghemite (γ-Fe 2 O 3 ) nanoparticles using temperature and time dependent magnetization. The average crystallite size for SiO 2 coated and uncoated nanoparticles was about 12 and 29 nm, respectively. Scanning electron microscopy (SEM) showed that the nanoparticles are spherical in shape and well separated. Temperature scans of zero field cooled (ZFC)/field cooled (FC) magnetization measurements showed lower average blocking temperature (T B ) for SiO 2 coated maghemite nanoparticles as compared to uncoated nanoparticles. The saturation magnetization (M s ) of SiO 2 coated maghemite nanoparticles was also lower than the uncoated nanoparticles and is attributed to smaller average crystallite size of SiO 2 coated nanoparticles. For saturation magnetization vs. temperature data, Bloch's law (M(T)= M(0).(1− BT b )) was fitted well for both uncoated and SiO 2 coated nanoparticles and yields: B =3×10 −7 K -b , b=2.22 and B=0.0127 K -b , b=0.57 for uncoated and SiO 2 coated nanoparticles, respectively. Higher value of B for SiO 2 coated nanoparticles depicts decrease in exchange coupling due to enhanced surface spins disorder (broken surface bonds) as compared to uncoated nanoparticles. The Bloch's exponent b was decreased for SiO 2 coated nanoparticles which is due to their smaller average crystallite size or finite size effects. Furthermore, a sharp increase of coercivity at low temperatures (<25 K) was observed for SiO 2 coated nanoparticles which is also due to contribution of increased surface anisotropy or frozen surface spins in these smaller nanoparticles. The FC magnetic relaxation data was fitted to stretched exponential law which revealed slower magnetic relaxation for SiO 2 coated nanoparticles. All these measurements revealed smaller average crystallite size and enhanced surface spins disorder in SiO 2 coated nanoparticles than in uncoated γ-Fe 2 O 3 nanoparticles

Preparation of Nd-doped BiFeO{sub 3} films and their electrical properties

Energy Technology Data Exchange (ETDEWEB)

Cheng Meng [Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education of China, Shaanxi University of Science and Technology, Weiyang District, Xi' an 710021 (China); Tan Guoqiang, E-mail: tan3114@163.com [Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education of China, Shaanxi University of Science and Technology, Weiyang District, Xi' an 710021 (China); Xue Xu; Xia Ao; Ren Huijun [Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education of China, Shaanxi University of Science and Technology, Weiyang District, Xi' an 710021 (China)

2012-09-01

The Nd-doped BiFeO{sub 3} thin films were prepared on SnO{sub 2}(FTO) substrates spin-coated by the sol-gel method using Nd(NO{sub 3}){sub 3}{center_dot}6H{sub 2}O, Fe(NO{sub 3}){sub 3}{center_dot}9H{sub 2}O and Bi(NO{sub 3}){sub 3}{center_dot}5H{sub 2}O as raw materials. The microstructure and electric properties of the BiFeO{sub 3} thin films were characterized and tested. The results indicate that the diffraction peak of the Nd-doped BiFeO{sub 3} films is shifted towards right as the doping amounts are increased. The structure is transformed from the rhombohedral to pseudotetragonal phase. The crystal grain is changed from an elliptical to irregular polyhedron. Structure transition occurring in the Bi{sub 0.85}Nd{sub 0.15}FeO{sub 3} films gives rise to the largest Pr of 64 {mu}C/cm{sup 2}. The leakage conductance of the Nd doped thin films is reduced. The dielectric constant and dielectric loss of Bi{sub 0.85}Nd{sub 0.15}FeO{sub 3} thin film at 10 kHz are 190 and 0.017 respectively.

Surface chemical and photocatalytic consequences of Ca-doping of BiFeO{sub 3} as probed by XPS and H{sub 2}O{sub 2} decomposition studies

Energy Technology Data Exchange (ETDEWEB)

Zaki, Mohamed I., E-mail: mizaki@link.net [Chemistry Department, Faculty of Science, Minia University, El-Minia 61519 (Egypt); Ramadan, Wegdan [Physics Department, Faculty of Science, Alexandria University, Alexandria 21511 (Egypt); Katrib, Ali [Chemistry Department, Faculty of Science, Kuwait University, P.O. Box 5969, Safat 13060 (Kuwait); Rabee, Abdallah I.M. [Chemistry Department, Faculty of Science, Minia University, El-Minia 61519 (Egypt)

2014-10-30

Graphical abstract: - Highlights: • BiFeO{sub 3} is a modest visible-light heterogeneous photocatalyst for H{sub 2}O{sub 2} decomposition. • The ferrite activity is promoted with Ca-doping up to 10 wt%-Ca. • Favourable consequences are enhanced surface metal redoxability and oxide basicity. • Furthering doping to >10 wt%-Ca retrogresses the ferrite photocatalytic activity. • A retrogressive doping consequence is bulk phase separation of α(γ)-Fe{sub 2}O{sub 3}. - Abstract: Pure and Ca-doped Bi{sub 1−x}Ca{sub x}FeO{sub 3} samples were prepared with x = 0.0–0.2, adopting a sol–gel method. Previously reported studies performed on similarly composed and prepared samples revealed that Ca-doping, above solubility limit (namely at ≥10%-Ca), results in phase separation and formation of BiFeO{sub 3}/α(γ)-Fe{sub 2}O{sub 3} nanocomposite particles. Hetero p/n nanojunctions thus established were considered to help separating photo-generated electron–hole pairs and, therefore, explain consequent promotion of photo-Fenton catalytic activity of BiFeO{sub 3} towards methylene blue degradation in presence of H{sub 2}O{sub 2} additive. However, the encompassed decomposition of H{sub 2}O{sub 2} was not addressed. To bridge this gap of knowledge, the present investigation was designed to assess Ca-doping-effected surface chemical modifications and gauge its impact on the heterogeneous photo-/thermo-catalytic activity of BiFeO{sub 3} towards H{sub 2}O{sub 2} decomposition, by means of X-ray photoelectron spectroscopy (XPS) and H{sub 2}O{sub 2} decomposition gravimetry. XPS results revealed generation of high binding energy Bi 4f and Fe 2p states, as well as enhancement of the surface basicity, upon doping to 10%-Ca. These surface chemical consequences are rendered hardly detectable upon further increase of the dopant magnitude to 20%-Ca. In parallel, the H{sub 2}O{sub 2} decomposition activity of the ferrite, under natural visible light, is enhanced to optimize

Novel three-dimensionally ordered macroporous Fe{sup 3+}-doped TiO{sub 2} photocatalysts for H{sub 2} production and degradation applications

Energy Technology Data Exchange (ETDEWEB)

Yan, Xiaoqing; Xue, Chao; Yang, Bolun; Yang, Guidong, E-mail: guidongyang@xjtu.edu.cn

2017-02-01

Highlights: • 3DOM Fe{sup 3+}-doped TiO{sub 2} photocatalyst was prepared. • 3DOM structure showed high activity for decomposition of the RhB and the generation of H{sub 2}. • 3DOM structure provided interfacial reaction sites and optical absorption active sites. • The energy level from Fe{sup 3+} centers were existed in the band gap of TiO{sub 2}. • 3DOM structure promoted the separation of charge carriers. - Abstract: Novel three-dimensionally ordered macroporous (3DOM) Fe{sup 3+}-doped TiO{sub 2} photocatalysts were prepared using a colloidal crystal template method with low-cost raw material including ferric trichloride, isopropanol, tetrabutyl titanate and polymethyl methacrylate. The as-prepared 3DOM Fe{sup 3+}-doped TiO{sub 2} photocatalysts were characterized by various analytical techniques. TEM and SEM results showed that the obtained photocatalysts possess well-ordered macroporous structure in three dimensional orientations. As proved by XPS and EDX analysis that Fe{sup 3+} ions have been introduced TiO{sub 2} lattice and the doped Fe{sup 3+} ions can act as the electron acceptor/donor centers to significantly enhance the electron transfer from the bulk to surface of TiO{sub 2}, resulting in more electrons could take part in the oxygen reduction process thereby decreasing the recombination rate of photogenerated charges. Meanwhile, the 3DOM architecture with the feature of interfacial chemical reaction active sites and optical absorption active sites is remarkably favorable for the reactant transfer and light trapping in the photoreaction process. As a result, the 3DOM Fe{sup 3+}-doped TiO{sub 2} photocatalysts show the considerably higher photocatalytic activity for decomposition of the Rhodamine B (RhB) and the generation of hydrogen under visible light irradiation due to the synergistic effects of open, interconnected macroporous network and metal ion doping.

Optimization of α-Fe{sub 2}O{sub 3}@Fe{sub 3}O{sub 4} incorporated N-TiO{sub 2} as super effective photocatalysts under visible light irradiation

Energy Technology Data Exchange (ETDEWEB)

Mohamed, Mohamed Mokhtar, E-mail: mohmok2000@yahoo.com [Benha University, Faculty of Science, Chemistry Department, Benha (Egypt); Bayoumy, W.A. [Benha University, Faculty of Science, Chemistry Department, Benha (Egypt); Goher, M.E. [National Institute of Oceanography & Fisheries, Environmental Chemistry, Cairo (Egypt); Abdo, M.H., E-mail: mh_omr@yahoo.com [National Institute of Oceanography & Fisheries, Environmental Chemistry, Cairo (Egypt); Mansour El-Ashkar, T.Y. [National Institute of Oceanography & Fisheries, Environmental Chemistry, Cairo (Egypt)

2017-08-01

Highlights: • The α-Fe{sub 2}O{sub 3}/Fe{sub 3}O{sub 4} doped n-TiO{sub 2} was synthesized via deposition-self assembly technique. • The photocatalyst 1%α-Fe{sub 2}O{sub 3}/Fe{sub 3}O{sub 4}/n-TiO{sub 2} show a remarkable performance while MB degradation. • The strong interaction between α-Fe{sub 2}O{sub 3}/Fe{sub 3}O{sub 4} and n-TiO{sub 2} plays an important role. • It exhibits a unique textural, optical and charge transfer properties. - Abstract: Well dispersed α-Fe{sub 2}O{sub 3}@Fe{sub 3}O{sub 4} nanoparticles (7 nm) supported on mesoporous nitrogen doped titanium dioxide (N-TiO{sub 2}) are synthesized by deposition self-assembly route and their performances as photocatalysts toward methylene blue (MB) degradation are evaluated. The results illustrate that the spherical yolk-shell structure of α-Fe{sub 2}O{sub 3}@Fe{sub 3}O{sub 4}@N-TiO{sub 2} at the loading of 1%; of excellent S{sub BET} (187 m{sup 2} g{sup −1}) and pore volume (0.50 cm{sup 3} g{sup −1}), achieved high photocatalytic performance for the MB degradation (20 ppm, λ > 420 nm, lamp power = 160 W) under visible light illumination (k = 0.059 min{sup −1}). The influence of the interface formation between α-Fe{sub 2}O{sub 3}@Fe{sub 3}O{sub 4} and n-TiO{sub 2} affects severely the charges separation efficiency and enhances the electron transfer to keep on the existence of Fe{sup 3+}/Fe{sup 2+} moieties; those take significant role in the reaction mechanism. The existence of the latter junction is affirmed via XRD, TEM-SAED, Raman and FTIR techniques whereas, the photogenerated charges, their separation together with their transport and recombination rates are depicted via photoluminescence, electrical conductivity, incident photon to current efficiency (IPCE), cyclic voltammetry (CV) and impedance (EIS) measurements. The catalyst loading, zero point charge, pH variation, total organic carbon (TOC%) and the effect of lamps power are thoroughly investigated. The 1%α-Fe{sub 2}O{sub 3

Ni doped Fe3O4 magnetic nanoparticles.

Science.gov (United States)

Larumbe, S; Gómez-Polo, C; Pérez-Landazábal, J I; García-Prieto, A; Alonso, J; Fdez-Gubieda, M L; Cordero, D; Gómez, J

2012-03-01

In this work, the effect of nickel doping on the structural and magnetic properties of Fe3O4 nanoparticles is analysed. Ni(x)Fe(3-x)O4 nanoparticles (x = 0, 0.04, 0.06 and 0.11) were obtained by chemical co-precipitation method, starting from a mixture of FeCl2 x 4H2O and Ni(AcO)2 x 4H2O salts. The analysis of the structure and composition of the synthesized nanoparticles confirms their nanometer size (main sizes around 10 nm) and the inclusion of the Ni atoms in the characteristic spinel structure of the magnetite Fe3O4 phase. In order to characterize in detail the structure of the samples, X-ray absorption (XANES) measurements were performed on the Ni and Fe K-edges. The results indicate the oxidation of the Ni atoms to the 2+ state and the location of the Ni2+ cations in the Fe2+ octahedral sites. With respect to the magnetic properties, the samples display the characteristic superparamagnetic behaviour, with anhysteretic magnetic response at room temperature. The estimated magnetic moment confirms the partial substitution of the Fe2+ cations by Ni2+ atoms in the octahedral sites of the spinel structure.

Synthesis and characterization of Fe3+ doped TiO2 nanoparticles and films and their performance for photocurrent response under UV illumination

International Nuclear Information System (INIS)

Elghniji, Kais; Atyaoui, Atef; Livraghi, Stefano; Bousselmi, Latifa; Giamello, Elio; Ksibi, Mohamed

2012-01-01

Graphical abstract: Schematic diagram illustrating the charge transfer from excited TiO 2 to the different states of Fe 3+ ions; C B and V B refer to the energy levels of the conduction and valence bands of TiO 2 , respectively. Highlights: ► In this study we examine the Iron as catalyst precursor to synthesize the Fe 3+ doped TiO 2 nanoparticles. ► The Fe 3+ doped TiO 2 catalysts show the presence of a mixed phase of anatase. ► The iron is completely absent in the XRD pattern of the doped iron TiO 2 powder. ► The analysis of EPR result further confirms that Fe 3+ ion are successfully doped in the TiO 2 lattice by substituting Ti 4+ . ► Fe 3+ doping can efficiently separate the photo-generated electrons and holes. - Abstract: Undoped TiO 2 and Fe 3+ doped (0.1, 0.3, 0.6 and 1 wt.%) TiO 2 nanoparticles have been synthesized by the acid-catalyzed sol–gel method. Iron cations are introduced in the initial solution, before gelification, what promotes their lattice localization. The Fe 3+ doped TiO 2 films have been fabricated using a dip-coating technique. The effect of iron content on the crystalline structure, phase transformation and grain growth were determined by X-ray diffraction (XRD), Raman spectroscopy, UV–visible diffused reflectance spectroscopy (DRS) and Electron paramagnetic resonance (EPR) spectroscopy. It has demonstrated that all catalysts are composed of mixed-phase crystals of anatase and brookite with anatase as dominant phase. The crystallinity of the brookite and anatase phases decreased with increasing the iron content. The analysis of EPR result further confirms that Fe 3+ ion are successfully doped in the TiO 2 lattice by substituting Ti 4+ . It was demonstrated that Fe 3+ ion in the TiO 2 films plays a role as the intermediate for the efficient separation of photogenerated hole–electron pairs and increases the photocurrent response of the film under UV light irradiation. The maximum photocurrent is obtained on the Fe 3+ doped TiO

Structural and photodegradation behaviors of Fe{sup 3+}-doping TiO{sub 2} thin films prepared by a sol–gel spin coating

Energy Technology Data Exchange (ETDEWEB)

Lin, Huey-Jiuan; Yang, Tien-Syh [Department of Materials Science and Engineering, National United University, 1 Lien-Da, Kung-Ching Li, Miao-Li 36003, Taiwan (China); Wang, Moo-Chin, E-mail: mcwang@kmu.edu.tw [Department of Fragrance and Cosmetic Science, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung 80782, Taiwan (China); Hsi, Chi-Shiung, E-mail: chsi@nuu.edu.tw [Department of Materials Science and Engineering, National United University, 1 Lien-Da, Kung-Ching Li, Miao-Li 36003, Taiwan (China)

2014-10-15

Highlights: • Pure and various Fe{sup 3+}-doped TiO{sub 2} thin films have been successfully fabricated. • The phase of all thin films was single phase of anatase TiO{sub 2} when calcined at 823 K. • The crystallinity of TiO{sub 2} thin films decreased as Fe{sup 3+}-doping increased. • The photodegradation of each sample increased as the irradiation time increased. • The photodegradation increased as Fe{sup 3+}-doping increased at a fixed irradiation time. - Abstract: Pure and various Fe{sup 3+}-doping TiO{sub 2} thin films have been successfully fabricated on glass substrate prepared by a sol–gel spin coating route. The structural and photodegradation behavior of these films after calcined at various temperatures for 1 h were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence (PL) spectrum and degradation of 1.0 × 10{sup −5} M methylene blue solution. When all thin films after calcined at 823 K for 1 h, the crystalline phase are comprised only contained single phase of anatase TiO{sub 2}. The crystallinity of various Fe{sup 3+}-doping TiO{sub 2} thin films decreases with Fe{sup 3+}-doping concentration increased. The PL intensity of all thin films also decreases with Fe{sup 3+}-doping concentration increased. When all various Fe{sup 3+}-doping TiO{sub 2} thin films after calcined at 823 K for 1 h, the photodegradation of each sample increases with irradiation time increased. Moreover, the photodegradation also increases with Fe{sup 3+}-doping concentration increased when fixed at constant irradiation time.

Photoelectrochemical Performance Observed in Mn-Doped BiFeO3 Heterostructured Thin Films

Directory of Open Access Journals (Sweden)

Hao-Min Xu

2016-11-01

Full Text Available Pure BiFeO3 and heterostructured BiFeO3/BiFe0.95Mn0.05O3 (5% Mn-doped BiFeO3 thin films have been prepared by a chemical deposition method. The band structures and photosensitive properties of these films have been investigated elaborately. Pure BiFeO3 films showed stable and strong response to photo illumination (open circuit potential kept −0.18 V, short circuit photocurrent density was −0.023 mA·cm−2. By Mn doping, the energy band positions shifted, resulting in a smaller band gap of BiFe0.95Mn0.05O3 layer and an internal field being built in the BiFeO3/BiFe0.95Mn0.05O3 interface. BiFeO3/BiFe0.95Mn0.05O3 and BiFe0.95Mn0.05O3 thin films demonstrated poor photo activity compared with pure BiFeO3 films, which can be explained by the fact that Mn doping brought in a large amount of defects in the BiFe0.95Mn0.05O3 layers, causing higher carrier combination and correspondingly suppressing the photo response, and this negative influence was more considerable than the positive effects provided by the band modulation.

Preparation and Study of NH3 Gas Sensing Behavior of Fe2O3 Doped ZnO Thick Film Resistors

Directory of Open Access Journals (Sweden)

D. R. Patil

2006-08-01

Full Text Available The preparation, characterization and gas sensing properties of pure and Fe2O3-ZnO mixed oxide semiconductors have been investigated. The mixed oxides were obtained by mixing ZnO and Fe2O3 in the proportion 1:1, 1:0.5 and 0.5:1. Pure ZnO was observed to be insensitive to NH3 gas. However, mixed oxides (with ZnO: Fe2O3 =1:0.5 were observed to be highly sensitive to ammonia gas. Upon exposure to NH3 gas, the barrier height of Fe2O3-ZnO intergranular regions decreases markedly due to the chemical transformation of Fe2O3 into well conducting ferric ammonium hydroxide leading to a drastic decrease in resistance. The crucial gas response was found to NH3 gas at 3500C and no cross response was observed to other hazardous and polluting gases. The effects of microstructure and doping concentration on the gas response, selectivity, response and recovery of the sensor in the presence of NH3 gas were studied and discussed.

Flow boiling heat transfer enhancement on copper surface using Fe doped Al{sub 2}O{sub 3}–TiO{sub 2} composite coatings

Energy Technology Data Exchange (ETDEWEB)

Sujith Kumar, C.S., E-mail: sujithdeepam@gmail.com [Department of Mechanical Engineering, National Institute of Technology, Tiruchirappalli 620015, Tamil Nadu (India); Suresh, S., E-mail: ssuresh@nitt.edu [Department of Mechanical Engineering, National Institute of Technology, Tiruchirappalli 620015, Tamil Nadu (India); Aneesh, C.R., E-mail: aneeshcr87@gmail.com [Department of Mechanical Engineering, National Institute of Technology, Tiruchirappalli 620015, Tamil Nadu (India); Santhosh Kumar, M.C., E-mail: santhoshmc@nitt.edu [Department of Physics, National Institute of Technology, Tiruchirappalli 620015, Tamil Nadu (India); Praveen, A.S., E-mail: praveen_as_1215@yahoo.co.in [Department of Mechanical Engineering, National Institute of Technology, Tiruchirappalli 620015, Tamil Nadu (India); Raji, K., E-mail: raji.kochandra@gmail.com [School of Nano Science and Technology, National Institute of Technology, Calicut 673601, Kerala (India)

2015-04-15

Graphical abstract: - Highlights: • Fe–Al{sub 2}O{sub 3}–TiO{sub 2} composite coatings were coated on the copper using spray pyrolysis. • Effect of Fe doping on porosity was determined using AFM. • Effect of Fe doping on hydrophilicity was determined. • Higher enhancement in CHF was obtained for 7.2 at% Fe doped coated sample. - Abstract: In the present work, flow boiling experiments were conducted to study the effect of spray pyrolyzed Fe doped Al{sub 2}O{sub 3}–TiO{sub 2} composite coatings over the copper heater blocks on critical heat flux (CHF) and boiling heat transfer coefficient. Heat transfer studies were conducted in a mini-channel of overall dimension 30 mm × 20 mm × 0.4 mm using de-mineralized water as the working fluid. Each coated sample was tested for two mass fluxes to explore the heat transfer performance. The effect of Fe addition on wettability and porosity of the coated surfaces were measured using the static contact angle metre and the atomic force microscope (AFM), and their effect on flow boiling heat transfer were investigated. A significant enhancement in CHF and boiling heat transfer coefficient were observed on all coated samples compared to sand blasted copper surface. A maximum enhancement of 52.39% and 44.11% in the CHF and heat transfer coefficient were observed for 7.2% Fe doped TiO{sub 2}–Al{sub 2}O{sub 3} for a mass flux of 88 kg/m{sup 2} s.

Electrochemical sensing behaviour of Ni doped Fe{sub 3}O{sub 4} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Suresh, R.; Giribabu, K.; Manigandan, R.; Narayanan, V., E-mail: vnnara@yahoo.co.in [Department of Inorganic Chemistry, University of Madras, Guindy Campus, Chennai 600 025 (India); Vijayalakshmi, L. [Annai Veilankanni' s College for Women (Arts and Science), Saidapet, Chennai 600015 (India); Stephen, A. [Department of Nuclear Physics, University of Madras, Guindy Campus, Chennai 600 025 (India)

2014-01-28

Ni doped Fe{sub 3}O{sub 4} nanoparticles were synthesized by simple hydrothermal method. The prepared nanomaterials were characterized by X-ray diffraction analysis, DRS-UV-Visible spectroscopy and field emission scanning electron microscopy. The XRD confirms the phase purity of the synthesized Ni doped Fe{sub 3}O{sub 4} nanoparticles. The optical property of Ni doped Fe{sub 3}O{sub 4} nanoparticles were studied by DRS UV-Visible analysis. The electrochemical sensing property of pure and Ni doped Fe{sub 3}O{sub 4} nanoparticles were examined using uric acid as an analyte. The obtained results indicated that the Ni doped Fe{sub 3}O{sub 4} nanoparticles exhibited higher electrocatalytic activity towards uric acid.

Influence of Fe doped on the magnetocaloric behavior of La_{{2}/{3}} Ca_{{1}/{3}} Mn1-x Fe x O3 compounds: a Monte Carlo simulation

Science.gov (United States)

Alzate-Cardona, J. D.; Barco-Rios, H.; Restrepo-Parra, E.

2018-02-01

The magnetocaloric behavior of La{2/{3}} Ca{1/{3}} Mn1-x Fe x O3 for x  =  0.00, 0.02, 0.03, 0.05, 0.07, 0.08 and 0.10 under the influence of an external magnetic field was simulated and analyzed. Simulations were carried out using the Monte Carlo method and the classical Heisenberg model under the Metropolis algorithm. These mixed valence manganites are characterized by having three types of magnetic ions corresponding to Mn4+≤ft(S=\\frac{3}{2}\\right) , which are bonded with Ca2+ , and Mneg3+ and Mneg\\prime3+ (S=2) , related to La3+ . The Fe ions were randomly included, replacing Mn ions. With this model, the magnetic entropy change, Δ S , in an isothermal process was determined. -Δ Sm showed maximum peaks around the paramagnetic-ferromagnetic transition temperature, which depends on Fe doping. Relative cooling power was computed for different Fe concentrations varying the magnetic applied field. Our model and results show that the Fe doping decreases the magnetocaloric effect in the La{2/{3}} Ca{1/{3}} Mn1-x Fe x O3, making this a bad candidate for magnetic refrigeration. The strong dependence of the magnetocaloric behavior on Fe doping and the external magnetic field in La{2/{3}} Ca{1/{3}} Mn1-x Fe x O3 can boost these materials for the future technological applications.

A comparative study of dissolution of {alpha}-Fe{sub 2}O{sub 3} and {gamma}-Fe{sub 2}O{sub 3} in DCD formulations

Energy Technology Data Exchange (ETDEWEB)

Ranganathan, S.; Raghavan, P.S.; Gopalan, R. [Madras Christian Coll. (India). Dept. of Chemistry; Srinivasan, M.P.; Narasimhan, S.V.

1998-12-31

The important corrosion products deposited on the surfaces of structural materials such as stainless steel in the primary coolant system of BWRs are haematite in the outer layers and ferrites such as magnetite, nickel ferrite, cobalt ferrite, etc., in the inner layers. Magnetite dissolution by 2, 6 Pyridinedicarboxylic acid (PDCA), Ethylenediaminetetraacetic acid (EDTA) and Nitrolotriacetic acid (NTA) showed that there is an optimum pH of dissolution for each ligand. The leaching of the metal ions from the oxides is controlled in part by reductive dissolution; this is due to the presence of Fe(II)-L complexes generated from the released Fe{sup 2+} ions. The addition of Fe(II)-L with the formulation greatly increases the rate of dissolution. In order to understand the role of Fe{sup 2+} arising from the spinel lattice of Fe{sub 3}O{sub 4} in aiding the dissolution of magnetite, it is appropriate to study the dissolution behaviour of the system like Fe{sub 2}O{sub 3} which is not containing any Fe{sup 2+} in the crystal lattice. The present study has been carried out with {alpha}-Fe{sub 2}O{sub 3} and {gamma}-Fe{sub 2}O{sub 3} in DCD formulation in the presence of ascorbic acid and with the addition of Fe(II)-L as a reductant. (author)

Enhanced multiferroic properties in scandium doped Bi2Fe4O9

International Nuclear Information System (INIS)

Dutta, Dimple P.; Tyagi, A. K.

2013-01-01

Undoped and Sc 3+ doped Bi 2 Fe 4 O 9 nanoparticles have been synthesized using sonochemical method. The phase purity of the samples was checked using powder X-rau diffraction technique. EDS analysis was done to confirm the extent of Sc 3+ doping in the samples. The size and morphology of the nanoparticles have been analyzed using transmission electron microscopy (TEM). The Bi 2 Fe 4 O 9 nanoparticles show a weak ferromagnetic behavior at room temperature, which is quite different from the linear M–H relationship reported for bulk Bi 2 Fe 4 O 9 . This is mainly attributed to the uncompensated moments at the disordered particle surface resulting from the reduced coordination of the surface spins, arising due to lattice strain or oxygen deficiency. Addition of Sc 3+ dopant in varying concentrations in these Bi 2 Fe 4 O 9 nanoparticles, improves their magnetic as well as ferroelectric properties. The leakage current is considerably reduced and electric polarization increases significantly in case of Bi 2 Fe 4(1-x) Sc x O 9 (x = 0.1) nanoparticles. Hence it can be inferred that Sc 3+ doped Bi 2 Fe 4 O 9 nanoparticles shows promise as good multiferroic materials.

Influences of the iron ion (Fe{sup 3+})-doping on structural and optical properties of nanocrystalline TiO{sub 2} thin films prepared by sol-gel spin coating

Energy Technology Data Exchange (ETDEWEB)

Ben Naceur, J. [Laboratoire de Photovoltaique de Semi-conducteurs et de Nanostructures, Centre de Recherche des Sciences et Technologies de l' Energie, BP.95, Hammam-Lif 2050 (Tunisia); Mechiakh, R., E-mail: raouf_mechiakh@yahoo.fr [Laboratoire de Photovoltaique de Semi-conducteurs et de Nanostructures, Centre de Recherche des Sciences et Technologies de l' Energie, BP.95, Hammam-Lif 2050 (Tunisia); Departement de Medecine, Faculte de Medecine, Universite Hadj Lakhdar, Batna (Algeria); Bousbih, F.; Chtourou, R. [Laboratoire de Photovoltaique de Semi-conducteurs et de Nanostructures, Centre de Recherche des Sciences et Technologies de l' Energie, BP.95, Hammam-Lif 2050 (Tunisia)

2011-10-01

Titanium dioxide (TiO{sub 2}) thin films doping of various iron ion (Fe{sup 3+}) concentrations were deposited on silicon (Si) (100) and quartz substrates by sol-gel Spin Coating technique followed by a thermal treatment at 600 deg. C. The structure, surface morphology and optical properties, as a function of the doping, have been studied by X-ray diffractometer (XRD), Raman, ultraviolet-visible (UV-vis) and Spectroscopic Ellipsometry (SE). XRD and Raman analyzes of our thin films show that the crystalline phase of TiO{sub 2} thin films comprised only the anatase TiO{sub 2}, but the crystallinity decreased when the Fe{sup 3+} content increased from 0% to 20%. During the Fe{sup 3+} addition to 20%, the phase of TiO{sub 2} thin film still maintained the amorphous state. The grain size calculated from XRD patterns varies from 29.3 to 22.6 nm. The complex index and the optical band gap (E{sub g}) of the films were determined by the spectroscopic ellipsometry analysis. We have found that the optical band gap decreased with an increasing Fe{sup 3+} content.

Synthesis and characterization of TiO2 photocatalyst doped by transition metal ions (Fe3+, Cr3+ and V5+)

International Nuclear Information System (INIS)

Tuan Vu, Anh; Linh Bui, Thi Hai; Cuong Tran, Manh; Phuong Dang, Tuyet; Hoa Tran, Thi Kim; Tuan Nguyen, Quoc

2010-01-01

Nano TiO 2 was synthesized by the hydrothermal method. The sample was doped with transition metal ions (V, Cr and Fe) and non-metal (N). Doped TiO 2 samples were characterized by x-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) and UV-Vis diffuse reflectance spectroscopy (UV-Vis). Photocatalytic activity in the mineralization of xylene (vapor phase), methylene blue and active dyer PR (liquid phase) was tested. In comparison with non-doped TiO 2 , V-, Cr-, Fe-doped TiO 2 and N-doped TiO 2 samples exhibited much higher photocatalytic activity using visible light instead of UV

Synergistic effects of F and Fe in co-doped TiO{sub 2} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yufei, E-mail: zhang.yu.fei@stu.xjtu.edu.cn; Shen, Huiyuan; Liu, Yanhua, E-mail: yhliu@mail.xjtu.edu.cn [Xi’an Jiaotong University, Department of Building Environment and Services Engineering, School of Human Settlements and Civil Engineering (China)

2016-03-15

TiO{sub 2} photocatalysts co-doped with F and Fe were synthesized by a sol–gel method. Synergistic effects of F and Fe in the co-doped TiO{sub 2} were verified by NH{sub 3} decomposition, X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS) and ultraviolet–visible (UV–Vis) absorption spectroscopy, and was analyzed by the simulation based on the density functional theory (DFT). The results from NH{sub 3} decomposition confirmed that the cooperation of F and Fe broadened the optical response of TiO{sub 2} to visible light region and also enhanced the photocatalytic activity of TiO{sub 2} under ultraviolet light. XRD patterns, SEM and HRTEM images showed that the co-doped samples were nanometric anatase with an average particle size of 25 nm. Co-doping with F and Fe inhibited the grain growth of TiO{sub 2} from anatase to rutile and resulted in a larger lattice defect. XPS analysis exhibited that the doped F and Fe atoms were into the TiO{sub 2} lattice. UV–Vis absorption spectra showed that its optical absorption edge was moved up to approximately 617 nm and its ultraviolet absorption was also enhanced. The DFT results indicated that the cooperation of Fe 3d and O 2p orbits narrowed the band gap of TiO{sub 2} and F 2p orbit widened the upper valence bands. The synergistic electron density around F and Fe in co-doped TiO{sub 2} was capable to enhance the photo-chemical stability of TiO{sub 2}.

Growth and characterization of ceria thin films and Ce-doped {gamma}-Al{sub 2}O{sub 3} nanowires using sol-gel techniques

Energy Technology Data Exchange (ETDEWEB)

Gravani, S; Polychronopoulou, K; Doumanidis, C C; Rebholz, C [Mechanical and Manufacturing Engineering Department, Engineering School, University of Cyprus, 1678, Nicosia (Cyprus); Stolojan, V; Hinder, S J; Baker, M A [Faculty of Engineering and Physical Sciences, University of Surrey, Guildford GU2 7XH (United Kingdom); Cui, Q; Gu, Z [Department of Chemical Engineering and CHN/NCOE Nanomanufacturing Center, University of Massachusetts Lowell, Lowell, MA 01854 (United States); Gibson, P N, E-mail: M.Baker@surrey.ac.uk [Institute for Health and Consumer Protection, Joint Research Centre of the European Commission, 21027 Ispra (Italy)

2010-11-19

{gamma}-Al{sub 2}O{sub 3} is a well known catalyst support. The addition of Ce to {gamma}-Al{sub 2}O{sub 3} is known to beneficially retard the phase transformation of {gamma}-Al{sub 2}O{sub 3} to {alpha}-Al{sub 2}O{sub 3} and stabilize the {gamma}-pore structure. In this work, Ce-doped {gamma}-Al{sub 2}O{sub 3} nanowires have been prepared by a novel method employing an anodic aluminium oxide (AAO) template in a 0.01 M cerium nitrate solution, assisted by urea hydrolysis. Calcination at 500 deg. C for 6 h resulted in the crystallization of the Ce-doped AlOOH gel to form Ce-doped {gamma}-Al{sub 2}O{sub 3} nanowires. Ce{sup 3+} ions within the nanowires were present at a concentration of < 1 at.%. On the template surface, a nanocrystalline CeO{sub 2} thin film was deposited with a cubic fluorite structure and a crystallite size of 6-7 nm. Characterization of the nanowires and thin films was performed using scanning electron microscopy, transmission electron microscopy, electron energy loss spectroscopy, x-ray photoelectron spectroscopy and x-ray diffraction. The nanowire formation mechanism and urea hydrolysis kinetics are discussed in terms of the pH evolution during the reaction. The Ce-doped {gamma}-Al{sub 2}O{sub 3} nanowires are likely to find useful applications in catalysis and this novel method can be exploited further for doping alumina nanowires with other rare earth elements.

Enhanced coercivity in Co-doped α-Fe2O3 cubic nanocrystal assemblies prepared via a magnetic field-assisted hydrothermal synthesis

Directory of Open Access Journals (Sweden)

Kinjal Gandha

2017-05-01

Full Text Available Ferromagnetic Co-doped α-Fe2O3 cubic shaped nanocrystal assemblies (NAs with a high coercivity of 5.5 kOe have been synthesized via a magnetic field (2 kOe assisted hydrothermal process. The X-ray diffraction pattern and Raman spectra of α-Fe2O3 and Co-doped α-Fe2O3 NAs confirms the formation of single-phase α-Fe2O3 with a rhombohedral crystal structure. Electron microscopy analysis depict that the Co-doped α-Fe2O3 NAs synthesized under the influence of the magnetic field are consist of aggregated nanocrystals (∼30 nm and of average assembly size 2 μm. In contrast to the NAs synthesized with no magnetic field, the average NAs size and coercivity of the Co-doped α-Fe2O3 NAs prepared with magnetic field is increased by 1 μm and 1.4 kOe, respectively. The enhanced coercivity could be related to the well-known spin–orbit coupling strength of Co2+ cations and the redistribution of the cations. The size increment indicates that the small ferromagnetic nanocrystals assemble into cubic NAs with increased size in the magnetic field that also lead to the enhanced coercivity.

Magnetic and dielectric properties of alkaline earth Ca2+ and Ba2+ ions co-doped BiFeO3 nanoparticles

International Nuclear Information System (INIS)

Yang, C.; Liu, C.Z.; Wang, C.M.; Zhang, W.G.; Jiang, J.S.

2012-01-01

Ca 2+ and Ba 2+ ions co-doped BiFeO 3 nanoparticles, Bi 0.8 Ca 0.2−x Ba x FeO 3 (x=0–0.20), were prepared by a sol–gel method. The phase structure, grain size, dielectric and magnetic properties of the prepared samples were investigated. The results showed that the lattice structure of the nanoparticles transformed from rhombohedral (x=0) to orthorhombic (x=0.07–0.19) and then to tetragonal (x=0.20) with x increased. The dielectric properties of the nanoparticles were affected by the properties of the substitutional ions as well as the crystalline structure of the samples. The magnetic properties of the nanoparticles were greatly improved and the T N of the nanoparticles was obviously increased. All the Ca 2+ and Ba 2+ ions co-doped BiFeO 3 nanoparticles presented the high ratio of M r /M from 0.527 to 0.571 and large coercivity from 4.335 to 5.163 KOe. - Highlights: ► Ca 2+ and Ba 2+ ions co-doped BiFeO 3 nanoparticles were prepared using a sol–gel method. ► The magnetic properties of the nanoparticles are greatly improved. ► The Neel temperature (T N ) of the nanoparticles is greatly increased. ► Doped ions and crystal structure affect the dielectric properties of the nanoparticles.

A Ti-doped γ-Fe2O3/SDS nano-photocatalyst as an efficient adsorbent for removal of methylene blue from aqueous solutions.

Science.gov (United States)

Mirbagheri, Naghmeh Sadat; Sabbaghi, Samad

2018-05-01

Synthetic dyes are among the most important environmental pollutants in wastewaters. Consequently, elimination of the synthetic dyes from wastewaters using non-toxic materials and eco-friendly technologies has been of considerable interests. In this study, magnetically separable Ti-doped γ-Fe 2 O 3 photocatalysts were synthesized for the removal of methylene blue (MB) from a dye-contaminated aqueous solution (as a model of dye-polluted wastewaters). Compared to the pristine γ-Fe 2 O 3 , the 1.78 v% Ti-doped γ-Fe 2 O 3 significantly increased the adsorption of MB by 57% in the dark condition as a result of the improved BET surface area in this photocatalyst. Moreover, the contact time required for the photocatalytic degradation of MB by the 1.78 v% Ti-doped γ-Fe 2 O 3 decreased due to the higher concentration of charge carriers in this photocatalyst than that of the pristine γ-Fe 2 O 3 . The effect of different experimental parameters on the adsorption property and photocatalytic activity of the 1.78 v% Ti-doped γ-Fe 2 O 3 photocatalyst showed that the solution pH had a remarkable influence on the removal performance of this photocatalyst. Surface treatment of the 1.78 v% Ti-doped γ-Fe 2 O 3 with sodium dodecyl sulfate (SDS) resulted in the formation of a negatively charged Ti-doped γ-Fe 2 O 3 /SDS photocatalyst, which showed a higher tendency for the adsorption and removal of MB than the untreated photocatalyst. Moreover, the MB removal efficiency of this photocatalyst was among the best performances that have been reported for the γ-Fe 2 O 3 -based photocatalysts. The synthesized photocatalysts were characterized by various techniques, and a plausible mechanism for the removal of MB from aqueous solutions by the Ti-doped γ-Fe 2 O 3 /SDS photocatalyst was purposed. Copyright © 2018 Elsevier Ltd. All rights reserved.

Enhanced photocatalytic property of BiFeO_3/N-doped graphene composites and mechanism insight

International Nuclear Information System (INIS)

Li, Pai; Li, Lei; Xu, Maji; Chen, Qiang; He, Yunbin

2017-01-01

Highlights: • A hydrothermal process was used to prepare BiFeO_3/N-doped graphene composites. • BiFeO_3/N-doped graphene exhibits superior photocatalytic activity and stability. • The energy band of BiFeO_3 bends downward by ∼1.0 eV at the composite interface. • Downward band bending leads to rapid electron transfer at the composite interface. • Holes and ·OH are predominant active species in the photo-degradation process. - Abstract: A series of BiFeO_3/(N-doped) graphene composites are prepared by a facile hydrothermal method. BiFeO_3/N-doped graphene shows photocatalytic performance superior to that of BiFeO_3/graphene and pristine BiFeO_3. The enhanced photo-degradation performance of BiFeO_3/N-doped graphene are mainly attributable to the improved light absorbance of the composite, abundant active adsorption sites and high electrical charge mobility of N-doped graphene, and the downward band bending of BiFeO_3 at the composite interface. In particular, X-ray photoelectron spectroscopy analyses reveal that the electron energy band of BiFeO_3 is downward bent by 1.0 eV at the interface of BiFeO_3/N-doped graphene, because of different work functions of both materials. This downward band bending facilitates the transfer of photogenerated electrons from BiFeO_3 to N-doped graphene and prompts the separation of photo-generated electron-hole pairs, leading eventually to the enhanced photocatalytic performance.

Co-precipitation synthesis and characterization of tin-doped α-Fe2O3 nanoparticles with enhanced photocatalytic activities

Science.gov (United States)

Mansour, Houda; Bargougui, Radhouane; Autret-Lambert, Cécile; Gadri, Abdellatif; Ammar, Salah

2018-03-01

In this study, Sn-doped hematite (α-Fe2O3) nanoparticles with various dopant concentrations ranging from 1 to 6 mol% were prepared successfully using a simple co-precipitation technique. The effects of Sn doping on the structural, morphological, optical, and magnetic properties were determined using X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), UV-visible diffuse reflectance spectroscopy, and a superconducting quantum interference device. XRD analysis showed that all of the samples had a typical hematite-type hexagonal structure of Fe2O3 without any additional peaks due to spurious phases. The cell parameters a and c decreased monotonically as the Sn content increased, thereby indicating that Sn ions were substituted into the α-Fe2O3 lattice. These results and the TEM analyses showed that the size of the nanoparticles decreased to 10 nm as the Sn doping concentration increased. UV-visible absorption measurements showed that the decrease in particle size was accompanied by a decrease in the band gap value from 2.07 eV for α-Fe2O3 to 1.87 eV with 6 mol% Sn doping. Furthermore, the magnetic properties demonstrated that all of the samples exhibited ferromagnetic behavior at room temperature. The photocatalytic activities of the samples were studied based on the degradation of methylene blue as a model compound, where the results showed that an appropriate amount of Sn dopant could greatly increase the amount of hydroxyl radicals generated by α-Fe2O3 nanoparticles, which were responsible for the obvious increase in the photocatalytic activity.

Surface spins disorder in uncoated and SiO{sub 2} coated maghemite nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Zeb, F. [Nanoscience and Technology Laboratory, International Islamic University, H-10, 44000 Islamabad (Pakistan); Nadeem, K., E-mail: kashif.nadeem@iiu.edu.pk [Nanoscience and Technology Laboratory, International Islamic University, H-10, 44000 Islamabad (Pakistan); Shah, S. Kamran Ali; Kamran, M. [Nanoscience and Technology Laboratory, International Islamic University, H-10, 44000 Islamabad (Pakistan); Gul, I. Hussain [School of Chemical & Materials Engineering, National University of Sciences and Technology (NUST), H-12, 44000 Islamabad, Pakistan (Pakistan); Ali, L. [Materials Research Laboratory, International Islamic University, H-10, 44000 Islamabad (Pakistan)

2017-05-01

We studied the surface spins disorder in uncoated and silica (SiO{sub 2}) coated maghemite (γ-Fe{sub 2}O{sub 3}) nanoparticles using temperature and time dependent magnetization. The average crystallite size for SiO{sub 2} coated and uncoated nanoparticles was about 12 and 29 nm, respectively. Scanning electron microscopy (SEM) showed that the nanoparticles are spherical in shape and well separated. Temperature scans of zero field cooled (ZFC)/field cooled (FC) magnetization measurements showed lower average blocking temperature (T{sub B}) for SiO{sub 2} coated maghemite nanoparticles as compared to uncoated nanoparticles. The saturation magnetization (M{sub s}) of SiO{sub 2} coated maghemite nanoparticles was also lower than the uncoated nanoparticles and is attributed to smaller average crystallite size of SiO{sub 2} coated nanoparticles. For saturation magnetization vs. temperature data, Bloch's law (M(T)= M(0).(1− BT{sup b})) was fitted well for both uncoated and SiO{sub 2} coated nanoparticles and yields: B =3×10{sup −7} K{sup -b}, b=2.22 and B=0.0127 K{sup -b}, b=0.57 for uncoated and SiO{sub 2} coated nanoparticles, respectively. Higher value of B for SiO{sub 2} coated nanoparticles depicts decrease in exchange coupling due to enhanced surface spins disorder (broken surface bonds) as compared to uncoated nanoparticles. The Bloch's exponent b was decreased for SiO{sub 2} coated nanoparticles which is due to their smaller average crystallite size or finite size effects. Furthermore, a sharp increase of coercivity at low temperatures (<25 K) was observed for SiO{sub 2} coated nanoparticles which is also due to contribution of increased surface anisotropy or frozen surface spins in these smaller nanoparticles. The FC magnetic relaxation data was fitted to stretched exponential law which revealed slower magnetic relaxation for SiO{sub 2} coated nanoparticles. All these measurements revealed smaller average crystallite size and enhanced surface

Pyrrolic-N-doped graphene oxide/Fe2O3 mesocrystal nanocomposite: Efficient charge transfer and enhanced photo-Fenton catalytic activity

Science.gov (United States)

Liu, Bing; Tian, Lihong; Wang, Ran; Yang, Jinfeng; Guan, Rong; Chen, Xiaobo

2017-11-01

Though α-Fe2O3 has attracted much attention in photocatalytic or Fenton-catalytic degradation of organic contaminants, its performance is still unsatisfactory due to fast recombination of electrons and holes in photocatalytic process and the difficult conversion of Fe(II) and Fe(III) in Fenton reaction. Herein, a pyrrolic N-doped graphene oxide/Fe2O3 mesocrystal (NG-Fe2O3) nanocomposite with good distribution is synthesized by a simple solvothermal method and adjusting the oxygen-containing groups on graphene oxide. The morphology of NG-Fe2O3 contributes to a relatively large BET surface area and an intimate contact between NG and Fe2O3. These two important factors along with the excellent electro-conductivity of pyrrolic-N doped GO result in the efficient separation of electron-hole pairs and fast conversion of Fe(II)and Fe(III) in photo-Fenton synergistic reaction. Thus, a remarkably improved photo-Fenton catalytic activity of NG-Fe2O3 is obtained. The degrading rate on methyl blue increases by 1.5 times and the conversion rate of glyphosate increases by 2.3 times under visible light irradiation, compared to pristine α-Fe2O3 mesocrystals.

Optical Properties and Photoactivity of The Pigmentary TiO2 Doped with P2O5, K2O, Al2O3 and Sb2O3

International Nuclear Information System (INIS)

Glen, M; Grzmil, B

2011-01-01

The influence of the increasing content of antimony calculated to Sb 2 O 3 (0.08-0.57 mol%) with the constant amount of the other additives (calculated to P 2 O 5 , K 2 O, Al 2 O 3 ) on the optical properties and photostability of doped rutile has been investigated. The properties of the obtained TiO 2 -PKAlSb samples were compared to the commercial TiO 2 -PKAl composition. The starting material was the concentrated suspension of technical-grade hydrated titanium dioxide (HTD). The dopant agents' solutions were introduced to HTD. Prepared samples were calcined with gradually increasing process temperature. The XRD analysis was used to determine the rutile content in the TiO 2 samples. Optical properties of modified titanium dioxide have been determined spectrophotometrically by measuring the colour in the white (brightness, white tone) and grey system (relative lightening power, grey tone). Photostability was characterized by the white lead-glycerin test with UV-Vis light. It was observed that with the increasing content of antimony in rutile TiO 2 , doped with phosphates, potassium and aluminium, the brightness and grey tone were increasing but white tone decreased. The changes of the relative lightening power values were insignificant. Comparing the samples of TiO 2 -PKAlSb with the TiO 2 -PKAl composition it was observed that titanium dioxide doped with antimony had better white and grey tone. The increasing Sb 2 O 3 content in the TiO 2 caused the improvement of the photostability.

Enhanced magnetic and ferroelectric properties in scandium doped nano Bi2Fe4O9

International Nuclear Information System (INIS)

Dutta, Dimple P.; Sudakar, C.; Mocherla, Pavana S.V.; Mandal, Balaji P.; Jayakumar, Onnatu D.; Tyagi, Avesh K.

2012-01-01

In this study we report the synthesis of undoped and Sc 3+ doped Bi 2 Fe 4 O 9 nanoparticles using sonochemical technique. X-ray diffraction reveals that all samples are single phase with no impurities detected. EDS analysis was done to confirm the extent of Sc 3+ doping in the samples. The size and morphology of the nanoparticles have been analyzed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The Bi 2 Fe 4 O 9 nanoparticles show a weak ferromagnetic behavior at room temperature, which is quite different from the linear M–H relationship reported for bulk Bi 2 Fe 4 O 9 . A magnetization of 0.144 μB/f.u. is obtained at 300 K, which is mainly attributed to the uncompensated moments at the disordered particle surface resulting from the reduced coordination of the surface spins, arising due to lattice strain or oxygen deficiency. Addition of Sc 3+ dopant in varying concentrations in these Bi 2 Fe 4 O 9 nanoparticles, improves their magnetic as well as ferroelectric properties. The leakage current is considerably reduced and electric polarization increases significantly in case of Bi 2 Fe 4(1−x) Sc x O 9 (x = 0.1) nanoparticles. Thus it can be inferred that Sc 3+ doped Bi 2 Fe 4 O 9 nanoparticles shows promise as good multiferroic materials. -- Graphical abstract: Undoped and Sc 3+ doped Bi 2 Fe 4 O 9 nanoparticles have been synthesized using sonochemical technique. The bi-functionalities of Sc 3+ doped Bi 2 Fe 4 O 9 nanoparticles have been demonstrated. The Bi 2 Fe 4(1−x) Sc x O 9 (x = 0.1) nanoparticles showed enhanced magnetic and ferroelectric properties with considerably less lossy characteristics compared to the bulk Bi 2 Fe 4 O 9 . Highlights: ► Phase pure Bi 2 Fe 4 O 9 nanostructures synthesized using a facile sonochemical technique. ► Nanoparticles show a weak ferromagnetic order at room temperature. ► Sc 3+ doping in Bi 2 Fe 4 O 9 nanoparticles alters their magnetic and ferroelectric properties. ► A

Sustained magnetization oscillations in polyaniline-Fe{sub 3}O{sub 4} nanocomposites

Energy Technology Data Exchange (ETDEWEB)

Araújo, A. C. V. de [Unidade Acadêmica de Garanhuns, Universidade Federal Rural de Pernambuco, Recife, Pernambuco (Brazil); Rodrigues, A. R., E-mail: ricalde@df.ufpe.br; Machado, F. L. A.; Rezende, S. M. [Departamento de Física, Universidade Federal de Pernambuco, 50670-901 Recife, Pernambuco (Brazil); Azevedo, W. M. de [Departamento de Química Fundamental, Universidade Federal de Pernambuco, 50670-901 Recife, Pernambuco (Brazil)

2015-09-28

We report experiments with polyaniline-Fe{sub 3}O{sub 4} (PANI-Fe{sub 3}O{sub 4}) nanocomposites synthesized under several different conditions. With a reaction carried out at room temperature and assisted by intense ultra-violet (UV) irradiation, we observe sustained oscillations in the magnetization with a period of about 25 min. The oscillations are interpreted as the result of an oscillatory chemical reaction in which part of the Fe{sup +2} ions of magnetite, Fe{sub 3}O{sub 4}, are oxidized by the UV irradiation to form Fe{sup +3} so that a fraction of the magnetite content transforms into maghemite, γ-Fe{sub 2}O{sub 3}. Then, Fe{sup +3} ions at the nanoparticle surfaces are reduced and transformed back into Fe{sup +2}, when acting as an oxidizing agent for polyaniline in the polymerization process. Since maghemite has smaller magnetization than magnetite, the oscillating chemical reaction results in the oscillatory magnetization. The observations are interpreted with the Lotka-Volterra nonlinear coupled equations with parameters that can be adjusted to fit very well the experimental data.

and α-Fe 2 O 3 nano powders synthesized by emulsion precipitation

African Journals Online (AJOL)

Nano crystals of γ-Fe2O3 (maghemite) were synthesized by emulsion precipitation method using kerosene as oil phase, SPAN- 80 (sorbitane monooleate) as the surfactant and sodium hydroxide as the precipitating agent. The characterization of the samples by FTIR (Fourier transform infra-red) and XRD (X-ray diffraction) ...

Structural transitions and multiferroic properties of high Ni-doped BiFeO3

Science.gov (United States)

Betancourt-Cantera, L. G.; Bolarín-Miró, A. M.; Cortés-Escobedo, C. A.; Hernández-Cruz, L. E.; Sánchez-De Jesús, F.

2018-06-01

Nickel doped bismuth ferrite powders, BiFe1-x NixO3 (0 ≤ x ≤ 0.5), were synthesized by high-energy ball milling followed by an annealing at 700 °C. A detailed study about the substitution of Fe3+ by Ni2+ on the crystal structure and multiferroic properties is presented. The X-ray diffraction patterns reveal the formation of rhombohedral structure with small amounts of Bi2Fe4O9 as a secondary phase for x behavior indicates the frustration of the G-antiferromagnetic order typical of the un-doped BiFeO3, caused by the presence of small amounts of Ni2+ (x Behavior modifications of electrical conductivity, permittivity and dielectric loss versus frequency are related with crystal structure transformations, when nickel concentration is increased.

Characterizations of diverse mole of pure and Ni-doped α-Fe2O3 synthesized nanoparticles through chemical precipitation route.

Science.gov (United States)

Sivakumar, S; Anusuya, D; Khatiwada, Chandra Prasad; Sivasubramanian, J; Venkatesan, A; Soundhirarajan, P

2014-07-15

In the present study, an attempt has been made for characterization and synthesis of pure and Ni-doped α-Fe2O3 (hematite) nanoparticles by chemical precipitation method. The synthesized products have been studied by X-ray diffraction (X-RD), Fourier transform infrared (FTIR) spectroscopy, UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS), vibrating sample magnetometer (VSM) and scanning electron microscopy (SEM) techniques. The estimated average diameter of α-Fe2O3 nanoparticles were calculated by using the Debye-Scherrer equation and established as 31 nm. SEM micrographs showed the surface morphology as well as structures and particles distributions of synthesized samples. The UV-Vis DRS showed the indirect and direct band gap energies of pure and Ni-doped α-Fe2O3, these were reduced from 1.9847 to 1.52 eV and 2.0503 to 1.76 eV respectively. This result suggested the dopant enhanced the semiconducting behavior of iron oxide nanoparticles to an extent proportional to its nickel doped in the α-Fe2O3. Further, the magnetic properties of the pure and doped samples were investigated by vibrating sample magnetometer (VSM) and evaluated the information of pure and doped samples exhibited saturated hysteresis loop at room temperature, which is indicating that the weak ferromagnetism in nature of our synthesized samples. In addition, it has been found from the magnetization hysteresis curves of Ni-doping, resulting from increased the saturation of magnetization and reduced the coercivity of used samples. Therefore, the present study showed the reduction in band gap energies and coercive field for α-Fe2O3 nanoparticles due to nickel doped. Copyright © 2014 Elsevier B.V. All rights reserved.

Synthesis and characterization of Fe{sup 3+} doped TiO{sub 2} nanoparticles and films and their performance for photocurrent response under UV illumination

Energy Technology Data Exchange (ETDEWEB)

Elghniji, Kais [University of Sfax, Laboratoire Eau, Energie et Environnement (LR3E), Ecole Nationale d' Ingenieurs de Sfax, B.P. 1173, 3038 Sfax (Tunisia); Atyaoui, Atef [Centre de Recherches et des Technologies des Eaux, Technopole de Borj Cedria B.P. 273, 8020 Soliman (Tunisia); Livraghi, Stefano [Dipartimento di Chimica I.F.M and NIS, Universita degli Studi di Torino, Via P. Giuria, 7 10125 Torino (Italy); Bousselmi, Latifa [Centre de Recherches et des Technologies des Eaux, Technopole de Borj Cedria B.P. 273, 8020 Soliman (Tunisia); Giamello, Elio [Dipartimento di Chimica I.F.M and NIS, Universita degli Studi di Torino, Via P. Giuria, 7 10125 Torino (Italy); Ksibi, Mohamed, E-mail: Mohamed.Ksibi@tunet.tn [University of Sfax, Laboratoire Eau, Energie et Environnement (LR3E), Ecole Nationale d' Ingenieurs de Sfax, B.P. 1173, 3038 Sfax (Tunisia)

2012-11-15

Graphical abstract: Schematic diagram illustrating the charge transfer from excited TiO{sub 2} to the different states of Fe{sup 3+} ions; C{sub B} and V{sub B} refer to the energy levels of the conduction and valence bands of TiO{sub 2}, respectively. Highlights: Black-Right-Pointing-Pointer In this study we examine the Iron as catalyst precursor to synthesize the Fe{sup 3+} doped TiO{sub 2} nanoparticles. Black-Right-Pointing-Pointer The Fe{sup 3+} doped TiO{sub 2} catalysts show the presence of a mixed phase of anatase. Black-Right-Pointing-Pointer The iron is completely absent in the XRD pattern of the doped iron TiO{sub 2} powder. Black-Right-Pointing-Pointer The analysis of EPR result further confirms that Fe{sup 3+} ion are successfully doped in the TiO{sub 2} lattice by substituting Ti{sup 4+}. Black-Right-Pointing-Pointer Fe{sup 3+} doping can efficiently separate the photo-generated electrons and holes. - Abstract: Undoped TiO{sub 2} and Fe{sup 3+} doped (0.1, 0.3, 0.6 and 1 wt.%) TiO{sub 2} nanoparticles have been synthesized by the acid-catalyzed sol-gel method. Iron cations are introduced in the initial solution, before gelification, what promotes their lattice localization. The Fe{sup 3+} doped TiO{sub 2} films have been fabricated using a dip-coating technique. The effect of iron content on the crystalline structure, phase transformation and grain growth were determined by X-ray diffraction (XRD), Raman spectroscopy, UV-visible diffused reflectance spectroscopy (DRS) and Electron paramagnetic resonance (EPR) spectroscopy. It has demonstrated that all catalysts are composed of mixed-phase crystals of anatase and brookite with anatase as dominant phase. The crystallinity of the brookite and anatase phases decreased with increasing the iron content. The analysis of EPR result further confirms that Fe{sup 3+} ion are successfully doped in the TiO{sub 2} lattice by substituting Ti{sup 4+}. It was demonstrated that Fe{sup 3+} ion in the TiO{sub 2} films

Mössbauer Studies of Core-Shell FeO/Fe3O4 Nanoparticles

Science.gov (United States)

Kamzin, A. S.; Valiullin, A. A.; Khurshid, H.; Nemati, Z.; Srikanth, H.; Phan, M. H.

2018-02-01

FeO/Fe3O4 nanoparticles were synthesized by thermal decomposition. Electron microscopy revealed that these nanoparticles were of the core-shell type and had a spherical shape with an average size of 20 nm. It was found that the obtained FeO/Fe3O4 nanoparticles had exchange coupling. The effect of anisotropy on the efficiency of heating (hyperthermic effect) of FeO/Fe3O4 nanoparticles by an external alternating magnetic field was examined. The specific absorption rate (SAR) of the studied nanoparticles was 135 W/g in the experiment with an external alternating magnetic field with a strength of 600 Oe and a frequency of 310 kHz. These data led to an important insight: the saturation magnetization is not the only factor governing the SAR, and the efficiency of heating of magnetic FeO/Fe3O4 nanoparticles may be increased by enhancing the effective anisotropy. Mössbauer spectroscopy of the phase composition of the synthesized nanoparticles clearly revealed the simultaneous presence of three phases: magnetite Fe3O4, maghemite γ-Fe2O3, and wustite FeO.

XAFS Studies of Fe Doped PhTiO3 Nanoparticles

International Nuclear Information System (INIS)

Shibata, Tomohiro; Chattopadhyay, Soma; Lin Bin; Palkar, V. R.

2007-01-01

Fe K and Ti K edge XAFS studies are reported on Fe doped PbTiO3 nanoparticles down to the 10 nm size. Fe forms Fe3+ ions and substitute for Ti4+ ions. For 18 nm nanoparticles, the Fe and Ti environment is found to be quite different. For PbFe0.5Ti0.5O3, locally the structure remains distorted from bulk to 10 nm size although the average structure changes

Efficiency of barium removal from radioactive waste water using the combination of maghemite and titania nanoparticles in PVA and alginate beads.

Science.gov (United States)

Majidnia, Zohreh; Idris, Ani; Majid, MuhdZaimiAbd; Zin, RosliMohamad; Ponraj, Mohanadoss

2015-11-01

In this paper, both maghemite (γ-Fe2O3) and titanium oxide (TiO2) nanoparticles were synthesized and mixed in various ratios and embedded in PVA and alginate beads. Batch sorption experiments were applied for removal of barium ions from aqueous solution under sunlight using the beads. The process has been investigated as a function of pH, contact time, temperature, initial barium ion concentration and TiO2:γ-Fe2O3 ratios (1:10, 1:60 and 1). The recycling attributes of these beads were also considered. Furthermore, the results revealed that 99% of the Ba(II) was eliminated in 150min at pH 8 under sunlight. Also, the maghemite and titania PVA-alginate beads can be readily isolated from the aqueous solution after the process and reused for at least 7 times without significant losses of their initial properties. The reduction of Ba(II) with maghemite and titania PVA-alginate beads fitted the pseudo first order and second order Langmuir-Hinshelwood (L-H) kinetic model. Copyright © 2015. Published by Elsevier Ltd.

Effect of titanium and calcium oxide additions on Zr2O2 polymorphism during Al2O3+Zr2O2 mixture fusion

International Nuclear Information System (INIS)

Gladkov, V.E.; Zhekhanova, N.B.; Fotiev, A.A.; Viktorov, V.V.; Ivashinnikov, V.T.; Zubov, A.S.

1985-01-01

The effect of titanium and calcium containing additions introduced into the Al 2 O 3 +ZrO 2 melt on the phase composition and temperature ranges of ZrO 2 polymorphous transformation in the material is investigated. It is shown that introducing sponge titanium into the 70Al 2 O 3 +30ZrO 2 prepared composition melt (mass. %) with its subsequent intensive cooling one can conserve upto room temperatures 50-70% of ZrO 2 metastable tetragonal modification and therefore reduce the volume changes causing metal cracking. Calcium oxide doping stabilizes the ZrO 2 cubic modification and reduces α-Al 2 O 3 content due to formation of aluminates

Fe-N co-doped SiO2@TiO2 yolk-shell hollow nanospheres with enhanced visible light photocatalytic degradation

Science.gov (United States)

Wan, Hengcheng; Yao, Weitang; Zhu, Wenkun; Tang, Yi; Ge, Huilin; Shi, Xiaozhong; Duan, Tao

2018-06-01

SiO2@TiO2 yolk@shell hollow nanospheres (STNSs) is considered as an outstanding photocatalyst due to its tunable structure and composition. Based on this point, we present an unprecedentedly excellent photocatalytic property of STNSs toward tannic acid via a Fe-N co-doped strategy. Their morphologies, compositions, structure and properties are characterized. The Fe-N co-doped STNSs formed good hollow yolk@shell structure. The results show that the energy gap of the composites can be downgraded to 2.82 eV (pure TiO2 = 3.2 eV). Photocatalytic degradation of tannic acid (TA, 30 mg L-1) under visible light (380 nm TiO2 nanospheres, non-doped STNSs and N-doped STNSs, the Fe-N co-doped STNSs exhibits the highest activity, which can degrade 99.5% TA into CO2 and H2O in 80 min. The probable degradation mechanism of the composites is simultaneously proposed, the band gap of STNSs becomes narrow by co-doping Fe-N, so that the TiO2 shell can stimulate electrons under visible light exposure, generate the ions of radOH and radO2- with a strong oxidizing property. Therefore this approach works is much desired for radioactive organic wastewater photocatalytic degradation.

Towards understanding the electronic structure of Fe-doped CeO2 nanoparticles with X-ray spectroscopy.

Science.gov (United States)

Wang, Wei-Cheng; Chen, Shih-Yun; Glans, Per-Anders; Guo, Jinghua; Chen, Ren-Jie; Fong, Kang-Wei; Chen, Chi-Liang; Gloter, Alexandre; Chang, Ching-Lin; Chan, Ting-Shan; Chen, Jin-Ming; Lee, Jyh-Fu; Dong, Chung-Li

2013-09-21

This study reports on the electronic structure of Fe-doped CeO2 nanoparticles (NPs), determined by coupled X-ray absorption spectroscopy and X-ray emission spectroscopy. A comparison of the local electronic structure around the Ce site with that around the Fe site indicates that the Fe substitutes for the Ce. The oxygen K-edge spectra that originated from the hybridization between cerium 4f and oxygen 2p states are sensitive to the oxidation state and depend strongly on the concentration of Fe doping. The Ce M(4,5)-edges and the Fe L(2,3)-edges reveal the variations of the charge states of Ce and Fe upon doping, respectively. The band gap is further obtained from the combined absorption-emission spectrum and decreased upon Fe doping, implying Fe doping introduces vacancies. The oxygen vacancies are induced by Fe doping and the spectrum reveals the charge transfer between Fe and Ce. Fe(3+) doping has two major effects on the formation of ferromagnetism in CeO2 nanoparticles. The first, at an Fe content of below 5%, is that the formation of Fe(3+)-Vo-Ce(3+) introduces oxygen deficiencies favoring ferromagnetism. The other, at an Fe content of over 5%, is the formation of Fe(3+)-Vo-Fe(3+), which favors antiferromagnetism, reducing the Ms. The defect structures Fe(3+)-Vo-Ce(3+) and Fe(3+)-Vo-Fe(3+) are crucial to the magnetism in these NPs and the change in Ms can be described as the effect of competitive interactions of magnetic polarons and paired ions.

Synthesis of γ–Fe2O3 nanoparticles with crystallographic and ...

African Journals Online (AJOL)

user

Maghemite (γ-Fe2O3) nanoparticles are synthesized by chemical ... In most of the reported methods, initially the particles have been synthesized in a non polar ... Carbon coated copper grid and was used for TEM characterization using an FEI ..... Currently he is Professor of Physics at IIT Kanpur working in the areas of ...

Experimental evidence of enhanced ferroelectricity in Ca doped BiFeO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Costa, L.V.; Deus, R.C. [Universidade Estadual Paulista, UNESP, Faculdade de Engenharia de Guaratinguetá, Av. Dr. Ariberto Pereira da Cunha, 333, Bairro Portal das Colinas, CEP 12516-410 Guaratinguetá, SP (Brazil); Foschini, C.R.; Longo, E. [Universidade Estadual Paulista, UNESP, Faculdade de Engenharia de Bauru, Dept. de Eng. Mecânica, Av. Eng. Luiz Edmundo C. Coube 14-01, 17033-360 Bauru, SP (Brazil); Cilense, M. [Universidade Estadual Paulista, UNESP, Instituto de Química – Laboratório Interdisciplinar em Cerâmica (LIEC), Rua Professor Francisco Degni s/n, 14800-90 Araraquara, SP (Brazil); Simões, A.Z., E-mail: alezipo@yahoo.com [Universidade Estadual Paulista, UNESP, Faculdade de Engenharia de Guaratinguetá, Av. Dr. Ariberto Pereira da Cunha, 333, Bairro Portal das Colinas, CEP 12516-410 Guaratinguetá, SP (Brazil)

2014-04-01

Calcium (Ca)-doped bismuth ferrite (BiFeO{sub 3}) thin films prepared by using the polymeric precursor method (PPM) were characterized by X-ray diffraction (XRD), field emission gun scanning electron microscopy (FEG-SEM), transmission electron microscopy (TEM), polarization and piezoelectric measurements. Structural studies by XRD and TEM reveal the co-existence of distorted rhombohedral and tetragonal phases in the highest doped BiFeO{sub 3} where enhanced ferroelectric and piezoelectric properties are produced by internal strain. Resistive switching is observed in BFO and Ca-doped BFO which are affected by the barrier contact and work function of multiferroic materials and Pt electrodes. A high coercive field in the hysteresis loop is observed for the BiFeO{sub 3} film. Piezoelectric properties are improved in the highest Ca-doped sample due to changes in the crystal structure of BFO for a primitive cubic perovskite lattice with four-fold symmetry and a large tetragonal distortion within the crystal domain. This observation introduces magnetoelectronics at room temperature by combining electronic conduction with electric and magnetic degrees of freedom which are already present in the multiferroic BiFeO{sub 3}. - Highlights: • Ca doped BiFeO{sub 3} thin films were obtained by the polymeric precursor method. • Co-existence of distorted rhombohedral and tetragonal phases are evident. • Enhanced ferroelectric and piezoelectric properties are produced by the internal strain in the Ca doped BiFeO{sub 3} film.

Selective Oxidation Using Flame Aerosol Synthesized Iron and Vanadium-Doped Nano-TiO2

Directory of Open Access Journals (Sweden)

Zhong-Min Wang

2011-01-01

Full Text Available Selective photocatalytic oxidation of 1-phenyl ethanol to acetophenone using titanium dioxide (TiO2 raw and doped with Fe or V, prepared by flame aerosol deposition method, was investigated. The effects of metal doping on crystal phase and morphology of the synthesized nanostructured TiO2 were analyzed using XRD, TEM, Raman spectroscopy, and BET nitrogen adsorbed surface area measurement. The increase in the concentration of V and Fe reduced the crystalline structure and the anatase-to-rutile ratios of the synthesized TiO2. Synthesized TiO2 became fine amorphous powder as the Fe and V concentrations were increased to 3 and 5%, respectively. Doping V and Fe to TiO2 synthesized by the flame aerosol increased photocatalytic activity by 6 folds and 2.5 folds, respectively, compared to that of pure TiO2. It was found that an optimal doping concentration for Fe and V were 0.5% and 3%, respectively. The type and concentration of the metal dopants and the method used to add the dopant to the TiO2 are critical parameters for enhancing the activity of the resulting photocatalyst. The effects of solvents on the photocatalytic reaction were also investigated by using both water and acetonitrile as the reaction medium.

CuO, MnO2 and Fe2O3 doped biomass ash as silica source for glass production in Thailand

Directory of Open Access Journals (Sweden)

N. Srisittipokakun

Full Text Available In this research, glass productions from rice husk ash (RHA and the effect of BaO, CuO, MnO2 and Fe2O3 on physical and optical properties were investigated. All properties were compared with glass made from SiO2 using same preparations. The results show that a higher density and refractive index of BaO, CuO, MnO2 and Fe2O3 doped in RHA glasses were obtained, compared with SiO2 glasses. The optical spectra show no significant difference between both glasses. The color of CuO glasses show blue from the absorption band near 800 nm (2B1g → 2B2g due to Cu2+ ion in octahedral coordination with a strong tetragonal distortion. The color of MnO2 glasses shows brown from broad band absorption at around 500 nm. This absorption band is assigned to a single allowed 5Eg → 5T2g transition which arises from the Mn3+ ions (3d4 configuration in octahedral symmetry. The yellow color derives from F2O3 glass due to the homogeneous distribution of Fe3+ (460 nm and Fe2+ (1050 nm ions in the glass matrices. Glass production from RHA is possible and is a new option for recycling waste from biomass power plant systems and air pollution reduction. Keywords: Rice husk ash, Glass, Optical, Physical

Photoluminescence quenching and enhanced spin relaxation in Fe doped ZnO nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Ovhal, Manoj M.; Santhosh Kumar, A. [Department of Materials Engineering, Defence Institute of Advanced Technology, Girinagar, Pune 411025 (India); Khullar, Prerna [School of Materials Science and Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005 (India); Kumar, Manjeet [Department of Materials Engineering, Defence Institute of Advanced Technology, Girinagar, Pune 411025 (India); Abhyankar, A.C., E-mail: ashutoshabhyankar@gmail.com [Department of Materials Engineering, Defence Institute of Advanced Technology, Girinagar, Pune 411025 (India)

2017-07-01

Cost-effective ultrasonically assisted precipitation method is utilized to synthesize Zinc oxide (ZnO) nanoparticles (NPs) at room temperature and the effect of Iron (Fe) doping on structural, optical and spin relaxation properties also presented. As-synthesized pure and Fe doped ZnO NPs possess a perfect hexagonal growth habit of wurtzite zinc oxide, along the (101) direction of preference. With Fe doping, ‘c/a’ ratio and compressive lattice strain in ZnO NPs are found to reduce and increase, respectively. Raman studies demonstrate that the E{sub 1} longitudinal optical (LO) vibrational mode is very weak in pure which remarkably enhanced with Fe doping into ZnO NPs. The direct band gap energy (E{sub g}) of the ZnO NPs has been increased from 3.02 eV to 3.11 eV with Fe doping. A slight red-shift observed with strong green emission band, in photoluminescence spectra, is strongly quenched in 6 wt.% Fe doped ZnO NPs. The field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) reveals spherical shape of ZnO NPs with 60–70 nm, which reduces substantially on Fe doping. The energy dispersive X-ray spectrum and elemental mapping confirms the homogeneous distribution of Fe in ZnO NPs. Moreover, the specific relaxation rate (R{sub 2sp} = 1/T{sub 2}) has been measured using Carr-Purcell-Meiboom-Gill (CPMG) method and found to be maximum in 6 wt.% Fe doped ZnO NPs. Further, the correlation of structural, optical and dynamic properties is proposed. - Highlights: • Pure ZnO and Fe doped ZnO NPs were successfully prepared by cost effective ultrasonically assisted precipitation method. • The optical band gap of ZnO has been enhanced form 3.02–3.11 eV with Fe doping. • PL quenching behaviour has been observed with Fe{sup 3+} ions substitution in ZnO lattice. • Specific relaxation rate (R{sub 2sp} = 1/T{sub 2}) has been varied with Fe doping and found to be maximum in 6 wt.% Fe doped ZnO NPs.

alpha-Fe2O3 versus beta-Fe2O3: Controlling the Phase of the Transformation Product of epsilon-Fe2O3 in the Fe2O3/SiO2 System

Czech Academy of Sciences Publication Activity Database

Brázda, Petr; Kohout, J.; Bezdička, Petr; Kmjec, T.

2014-01-01

Roč. 14, č. 3 (2014), s. 1039-1046 ISSN 1528-7483 R&D Projects: GA ČR GAP204/10/0035 Institutional support: RVO:61388980 Keywords : CHEMICAL-VAPOR-DEPOSITION * OXIDE THIN-FILMS * X-RAY * GAMMA-FE2O3 NANOPARTICLES * THERMAL-DECOMPOSITION Subject RIV: CA - Inorganic Chemistry Impact factor: 4.891, year: 2014

Synthesis and characterization of Fe-doped TiO2 photocatalyst by the sol–gel method

International Nuclear Information System (INIS)

Luu, Cam Loc; Ho, Si Thoang; Nguyen, Quoc Tuan

2010-01-01

Thin layers of pure TiO 2 and TiO 2 doped by different amounts of Fe 2 O 3 have been prepared by the sol–gel method with tetraisopropyl orthotitanate and Fe(NO 3 ) 3 . Physico-chemical properties of catalysts were characterized by BET Adsorption, x-ray Diffraction (XRD), FE-SEM, as well as Raman and UV-Vis spectroscopy. The photocatalytic activity of the obtained materials was investigated in the reaction of complete oxidation of p-xylene in gas phase under the radiation of UV (λ=365 nm) and LED (λ=470 nm) lamps. It has been found that the particle size of all samples was distributed in the range 20–30 nm. The content of the rutile phase in Fe-doped TiO 2 samples varied in the range 6.8 to 41.8% depending on the Fe content. Iron oxide doped into TiO 2 enables the photon absorbing zone of TiO 2 to extend from UV towards visible waves as well as to reduce its band gap energy from 3.2 to 2.67 eV. Photocatalytic activities of the TiO 2 samples modified by Fe 3+ have been found to be higher than those of pure TiO 2 by about 2.5 times

Vacancy ordered γ-Fe{sub 2}O{sub 3} nanoparticles functionalized with nanohydroxyapatite: XRD, FTIR, TEM, XPS and Mössbauer studies

Energy Technology Data Exchange (ETDEWEB)

Ramos Guivar, Juan A., E-mail: juan.ramos5@unmsm.edu.pe [Faculty of Physical Sciences, National University of San Marcos, P. O. Box 14- 0149, Lima 14 (Peru); Sanches, Edgar A., E-mail: sanches.ufam@gmail.com [Federal University of Amazonas, Department of Physics, Manaus/AM (Brazil); Bruns, Florian, E-mail: f.bruns@tu-braunschweig.de [Institut für Physik der Kondensierten Materie, Technische Universität Braunschweig, 38110 Braunschweig (Germany); Sadrollahi, Elaheh, E-mail: elahe.sadrollahi@gmail.com [Institut für Physik der Kondensierten Materie, Technische Universität Braunschweig, 38110 Braunschweig (Germany); Morales, M.A., E-mail: marco.moralestorres@gmail.com [Department of Theoretical and Experimental Physics, UFRN, Natal, RN 59078- 970 (Brazil); López, Elvis O., E-mail: lopmezel@gmail.com [Brazilian Center for Research in Physics (CBPF), Rio de Janeiro, RJ 22290-180 (Brazil); Litterst, F. Jochen, E-mail: litterst@cbpf.br [Institut für Physik der Kondensierten Materie, Technische Universität Braunschweig, 38110 Braunschweig (Germany); Brazilian Center for Research in Physics (CBPF), Rio de Janeiro, RJ 22290-180 (Brazil)

2016-12-15

Graphical abstract: Possible bonding configuration in the γ-Fe{sub 2}O{sub 3} nanoparticles functionalized with nanoHAp. - Highlights: • Coprecipitation in alkaline medium for the synthesis of vacancy ordered γ-Fe{sub 2}O{sub 3}@HAp nanocomposite. • Samples were characterized by XRD, FTIR, XPS, TEM, VSM and Mössbauer spectroscopy. • The functionalization is explained with the binding of two oxygens of chemisorbed H{sub 2}O molecules at the common interface of HAp/C{sub 6}H{sub 8}O{sub 7}/γ-Fe{sub 2}O{sub 3}. - Abstract: Vacancy ordered maghemite (γ-Fe{sub 2}O{sub 3}) nanoparticles functionalized with nanohydroxyapatite (HAp – Ca{sub 10}(PO{sub 4}) {sub 6}(OH){sub 2}) have been successfully synthesized using an inexpensive co-precipitation chemical route. Evidence for the presence of vacancy order in maghemite was shown by the superstructure lines observed in X-ray diffraction. The adsorption of carboxyl groups of citric acid (C{sub 6}H{sub 8}O{sub 7}) onto γ-Fe{sub 2}O{sub 3} nanoparticles was investigated by FTIR, XPS and Mössbauer spectroscopy. From XPS surface analysis, two binding energies related to oxygen were attributed to bindings between C{sub 6}H{sub 8}O{sub 7}/γ- Fe{sub 2}O{sub 3} and C{sub 6}H{sub 8}O{sub 7}/HAp from an interfacial reaction promoted by strongly adsorbed H{sub 2}O molecules at the surface of these nanomaterials. Le Bail refinement of the XRD patterns showed the formation of well-crystallized pure tetragonal maghemite before and after functionalization with nanoHAp. The temperature dependence of hyperfine parameters of pure and functionalized γ-Fe{sub 2}O{sub 3} nanoparticles was investigated via Mössbauer spectroscopy. TEM revealed the formation of quasi-spherical γ- Fe{sub 2}O{sub 3} nanoparticles with an average diameter of ca. 12 nm and 16 nm before and after functionalization with nanoHAp in agreement with Le Bail refinement. Magnetometry measurements showed a saturation magnetization of 12 emu/g and a blocking

A close correlation between induced ferromagnetism and oxygen deficiency in Fe doped In2O3

International Nuclear Information System (INIS)

Singhal, R.K.; Samariya, A.; Kumar, Sudhish; Sharma, S.C.; Xing, Y.T.; Deshpande, U.P.; Shripathi, T.; Saitovitch, E.

2010-01-01

We report on the reversible manipulation of room temperature ferromagnetism in Fe (5%) doped In 2 O 3 polycrystalline magnetic semiconductor. The X-ray diffraction and photoemission measurements confirm that the Fe ions are well incorporated into the lattice, substituting the In 3+ ions. The magnetization measurements show that the host In 2 O 3 has a diamagnetic ground state, while it shows weak ferromagnetism at 300 K upon Fe doping. The as-prepared sample was then sequentially annealed in hydrogen, air, vacuum and finally in air. The ferromagnetic signal shoots up by hydrogenation as well as vacuum annealing and bounces back upon re-annealing the samples in air. The sequence of ferromagnetism shows a close inter-relationship with the behavior of oxygen vacancies (V o ). The Fe ions tend to a transform from 3+ to 2+ state during the giant ferromagnetic induction, as revealed by photoemission spectroscopy. A careful characterization of the structure, purity, magnetic, and transport properties confirms that the ferromagnetism is due to neither impurities nor clusters but directly related to the oxygen vacancies. The ferromagnetism can be reversibly controlled by these vacancies while a parallel variation of carrier concentration, as revealed by resistance measurements, appears to be a side effect of the oxygen vacancy variation.

Hydrothermal synthesis of Fe-doped TiO2 nanostructure photocatalyst

International Nuclear Information System (INIS)

Nguyen, Van Nghia; Nguyen, Ngoc Khoa Truong; Nguyen, Phi Hung

2011-01-01

Fe-doped TiO 2 catalyst was prepared by the hydrothermal method. The resulting nanopowders were characterized by x-ray diffraction, transmission electron microscopy and Raman and UV-visible spectroscopies. The photocatalytic activity of the Fe-doped TiO 2 was tested by decomposition of methylene orange with a concentration of 10 mg l −1 in aqueous solution. The obtained results showed that methylene orange was significantly degraded after irradiation for 90 min under a halogen lamp and sunlight. The doping effect on the photocatalytic activity of the iron-doped catalyst samples are discussed

Synthesis and characterization of Cr doped CoFe2O4

Science.gov (United States)

Verma, Kavita; Patel, K. R.; Ram, Sahi; Barbar, S. K.

2016-05-01

Polycrystalline samples of pure and Cr-doped cobalt ferrite (CoFe2O4 and CoCrFeO4) were prepared by solid state reaction route method. X-ray diffraction pattern infers that both the samples are in single phase with Fd3m space group. Slight reduction in the lattice parameter of CoCrFeO4 has been observed as compared to CoFe2O4. The dielectric dispersion has been explained on the basis of Fe2+ ↔ Fe3+ hopping mechanism. The polarizations at lower frequencies are mainly attributed to electronic exchange between Fe2+ ↔ Fe3+ ions on the octahedral site in the ferrite lattice. In the present system a part from n-type charge carrier (Fe3+/Fe2+), the presence of (Co3+/Co2+) ions give rise to p-type charge carrier. Therefore in addition to n-type charge carrier, the local displacement of p-type charge carrier in direction of external electric field also contributes to net polarization. However, the dielectric constant and loss tangent of CoCrFeO4 are found to be lower than CoFe2O4 and is attributed to the availability of ferrous ion. CoCrFeO4 have less amount of ferrous ion available for polarization as compared to that of CoFe2O4. The impedance spectra reveal a grain interior contribution to the conduction process.

Dynamics in γ-Fe₂O₃ nanoparticles studied by time-of-flight polarized neutron scattering

DEFF Research Database (Denmark)

Kuhn, L.T.; Lefmann, K.; Klausen, S.N.

2004-01-01

The inelastic neutron-scattering signal from magnetic nanoparticles contains information on magnetic dynamics like superparamagnetic relaxation and collective magnetic excitations. Often another, very broad quasi-elastic component is observed in addition. We have studied this quasi-elastic neutron...... signal from 4 nm ferrimagnetic maghemite (gamma-Fe(2)O(3)) particles, and by means of time-of-flight polarised neutron scattering we have identified the source of (most of) this signal to be water adsorbed at the surface of the nanoparticles. A minor part of the signal has its origin in dynamics...

Photocatalytic and microwave absorbing properties of polypyrrole/Fe-doped TiO2 composite by in situ polymerization method

International Nuclear Information System (INIS)

Li Qiaoling; Zhang Cunrui; Li Jianqiang

2011-01-01

Research highlights: → Polypyrrole/Fe-doped TiO 2 composite is prepared by in situ polymerization of pyrrole on the Fe-doped TiO 2 template. → The Fe-doped TiO 2 microbelts are prepared by sol-gel method using the absorbent cotton template for the first time. → Then the Fe-doped TiO 2 microbelts are used as template for the preparation of polypyrrole/Fe-doped TiO 2 composites. → The structure, morphology and properties of the composites are characterized with scanning electron microscope (SEM), IR, Net-work Analyzer. → A possible formation mechanism of Fe-doped TiO 2 microbelts and polypyrrole/Fe-doped TiO 2 composites has been proposed. → The effect of the mol ratio of pyrrole/Fe-doped TiO 2 on the photocatalysis properties and microwave loss properties of the composites is investigated. - Abstract: The Fe-doped TiO 2 microbelts were prepared by sol-gel method using the absorbent cotton template for the first time. Then the Fe-doped TiO 2 microbelts were used as templates for the preparation of polypyrrole/Fe-doped TiO 2 composites. Polypyrrole/Fe-doped TiO 2 composites were prepared by in situ polymerization of pyrrole on the Fe-doped TiO 2 template. The structure, morphology and properties of the composites were characterized with scanning electron microscope (SEM), FTIR, Net-work Analyzer. The possible formation mechanisms of Fe-doped TiO 2 microbelts and polypyrrole/Fe-doped TiO 2 composites have been proposed. The effect of the molar ratio of pyrrole/Fe-doped TiO 2 on the photocatalytic properties and microwave loss properties of the composites was investigated.

Decomposition mechanism of methylene blue caused by metallic iron-maghemite mixture

Energy Technology Data Exchange (ETDEWEB)

Kubuki, Shiro, E-mail: kubuki@tmu.ac.jp; Shibano, Koya; Akiyama, Kazuhiko [Tokyo Metropolitan University, Department of Chemistry, Graduate School of Science and Engineering (Japan); Homonnay, Zoltan; Kuzmann, Erno [Eoetvoes Lorand University, Laboratory of Nuclear Chemistry, Institute of Chemistry (Hungary); Ristic, Mira [Ruder Boskovic Institute, Division of Materials Chemistry (Croatia); Nishida, Tetsuaki [Kinki University, Department of Biological and Environmental Chemistry, Faculty of Humanity-Oriented Science and Engineering (Japan)

2013-04-15

Decomposition mechanism of methylene blue (MB) caused by a mixture of metallic iron-maghemite (Fe{sup 0}-{gamma}Fe{sub 2}O{sub 3}) was investigated by means of {sup 57}Fe-Moessbauer spectroscopy, X-ray diffractometry (XRD), Ultraviolet-Visible Absorption Spectroscopy (UV-vis) and electrospray-ionization mass spectroscopy (ESI-MS). Ten day-leaching test of 10 {mu}mol L{sup - 1} MB aqueous solution and Fe{sup 0}-{gamma}Fe{sub 2}O{sub 3} mixture (mass ratio 3:7) showed a decrease in the concentration from 10.5 to 4.45 {mu}mol L{sup - 1} with first-order rate constant (k) of 1.57 x 10 - 1 day - 1. An ESI-MS study of Fe{sup 0}-{gamma}Fe{sub 2}O{sub 3} mixture (3:7) after the leaching test revealed new peaks at m/z of 100, 110 and 137 due to fragmentation of MB, in addition to those observed at m/z of 284, 270 and 256 which were ascribed to MB, Azure B and Azure A, respectively. {sup 57}Fe-Moessbauer spectra of Fe{sup 0}-{gamma}Fe{sub 2}O{sub 3} mixture (3:7) resulted in a decrease in absorption area (A) for Fe{sup 0} ({delta} = 0.00{sub {+-}0.01} mm s{sup - 1}, H{sub int} = 33.0{sub {+-}0.1} T) from 37.5 to 21.3, 9.7, 7.9, 7.0 and 4.5{sub {+-}0.5} %, together with an increase in A from 0.0 to 5.0, 13.8, 17.2, 21.0 and 22.4{sub {+-}0.5} % for octahedral (O{sub h}) iron (Fe{sup II} + Fe{sup III}) of Fe{sub 3}O{sub 4}. XRD study of these samples indicated that the peak intensity at 2{Theta} of 44.7 Degree-Sign being ascribed to Fe{sup 0} was decreased, while that of 35.6 Degree-Sign due to Fe{sub 3}O{sub 4} was almost constant; relative peak ratio of Fe {sup 0}/Fe{sub 3} O{sub 4} was decreased from 26.3 to 2.76 after the leaching, indicating that Fe{sup 0} in the Fe{sup 0}-{gamma}Fe{sub 2}O{sub 3} mixture was oxidized to Fe{sub 3}O{sub 4}. These experimental results suggest that Fe{sup 0}-{gamma}Fe{sub 2}O{sub 3} mixture could be utilized for the cleaning or decomposition of toxic organic compounds like trichloroethylene.

Improvement of tribological properties of magnetic tape by silica coating onto the Co-{gamma}-Fe{sub 2}O{sub 3} fine particles; Kobaruto hichakugata {gamma}-Fe{sub 2}O{sub 3} jisei biryushi no shisshiki shirika hyomen shori ni yoru jikitepu no suberi tokusei no kaizen

Energy Technology Data Exchange (ETDEWEB)

Hayashi, Kazuyuki; Iwasaki, Keisuke; Tanaka, Yasuyuki; Morii, Hiroko [Toda Kogyo Corporation, Hiroshima (Japan). R and D Center

1999-01-10

In order to improve the tribological properties of magnetic tape with Co-{gamma}-Fe{sub 2}O{sub 3} fine particles against a magnetic head, the silica coating onto the surface of Co-{gamma}-Fe{sub 2}O{sub 3} particles in aqueous slurry is investigated experimentally, and the kinetic friction coefficient of magnetic tapes prepared using the coated particles is measured. By this silica coating, the amount of myristic acid absorbed on the Co-{gamma}-Fe{sub 2}O{sub 3} particles tends to decrease and the kinetic friction coefficient of the magnetic tapes can be reduced from 0.4 to 0.2 because of the increase of the effective amount of myristic acid working as the lubricant when the magnetic tape is moving. Since the magnetic properties and the dispersibility of Co-{gamma}-Fe{sub 2}O{sub 3} pigment in the magnetic lacquer are not degraded by the silica coating, this coating method is expected to result in magnetic recording media with both good magnetic and low friction properties. (author)

Effect of Nd-doping on structure and microwave electromagnetic properties of BiFeO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Liu, Sheng [School of Physics and Electronics, Institute of Super-microstructure and Ultrafast Process in Advanced Materials, Central South University, Changsha 410083 (China); Luo, Heng [State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Yan, Shuoqing; Yao, Lingling; He, Jun; Li, Yuhan; He, Longhui; Huang, Shengxiang; Deng, Lianwen [School of Physics and Electronics, Institute of Super-microstructure and Ultrafast Process in Advanced Materials, Central South University, Changsha 410083 (China)

2017-03-15

The single-phase Bi{sub 1-x}Nd{sub x}FeO{sub 3} (x=0, 0.05, 0.10, 0.15, 0.20) were synthesized by the sol-gel method. Their crystal structure and microwave electromagnetic property in the frequency range of 2–18 GHz were investigated. The XRD patterns and Raman spectra showed that structural transition from rhombohedral (x=0, 0.05, 0.1) to triclinic (x=0.15) and tetragonal structure (x=0.20) appeared in the Bi{sub 1-x}Nd{sub x}FeO{sub 3}. Electromagnetic measurement suggested that both microwave permeability μ′ and magnetic loss tanδ{sub m} increased remarkably over 2–18 GHz by doping Nd. Strong dielectric loss peak was observed on the samples of Bi{sub 1-x}Nd{sub x}FeO{sub 3} (x=0.15) and Bi{sub 1-x}Nd{sub x}FeO{sub 3} (x=0.2). Results show that Nd substitution is an effective way to push BiFeO{sub 3} to become microwave absorbing materials with high performance. - Highlights: • Single-phase Bi{sub 1-x}Nd{sub x}FeO{sub 3} samples were prepared by a sol-gel method. • Strong dielectric loss peak was observed in BiFeO{sub 3} with high doping content. • Significant enhancement of microwave absorption property was found in Nd-doped BiFeO{sub 3}.

Crystalline and Electronic Structures and Magnetic and Electrical Properties of La-Doped Ca2Fe2O5 Compounds

Science.gov (United States)

Phan, T. L.; Tho, P. T.; Tran, N.; Kim, D. H.; Lee, B. W.; Yang, D. S.; Thiet, D. V.; Cho, S. L.

2018-01-01

Brownmillerite Ca2Fe2O5 has been observed to exhibit many outstanding properties that are applicable to ecotechnology. However, very little work on doped Ca2Fe2O5 compounds has been carried out to widen their application scope. We present herein a detailed study of the crystalline/geometric and electronic structures and magnetic and electrical properties of Ca2- x La x Fe2O5 ( x = 0 to 1) prepared by conventional solid-state reaction. X-ray diffraction patterns indicated that the compounds with x = 0 to 0.05 exhibited brownmillerite-type single phase. La doping with higher content ( x ≥ 0.1) stimulated additive formation of Grenier- (LaCa2Fe3O8) and perovskite-type (LaFeO3) phases. Extended x-ray absorption fine structure spectroscopy at the Fe K-edge and electron spin resonance spectroscopy revealed presence of Fe3+ in the parent Ca2Fe2O5 ( x = 0) and both Fe3+ and Fe4+ in the doped compounds ( x ≥ 0.05). The Fe4+ content tended to increase with increasing x. This stimulates ferromagnetic exchange interactions between Fe3+ and Fe4+ ions and directly influences the magnetic properties of Ca2- x La x Fe2O5. Electrical resistivity ( ρ) measurements in the temperature range of T = 20 K to 400 K revealed that all the compounds exhibit insulator behavior; the ρ( T) data for x ≥ 0.1 could be described based on the adiabatic small polaron hopping model.

Interfaces exchange bias and magnetic properties of ordered CoFe_2O_4/Co_3O_4 nanocomposites

International Nuclear Information System (INIS)

Zhang, B.B.; Xu, J.C.; Wang, P.F.; Han, Y.B.; Hong, B.; Jin, H.X.; Jin, D.F.; Peng, X.L.; Li, J.; Yang, Y.T.; Gong, J.; Ge, H.L.; Wang, X.Q.

2015-01-01

Graphical abstract: - Highlights: • CoFe_2O_4 nanoparticles were well-dispersed anchored in mesopores of Co_3O_4. • The magnetic behavior of nanocomposites changed greatly at low temperature. • CoFe_2O_4 nanoparticles reinforced the interfaces magnetic interaction of nanocomposites. • M increased with the doping of CoFe_2O_4 and the decreasing temperature. • Exchange bias effect was observed at 100 K and increased with the doping of CoFe_2O_4. - Abstract: Cobalt ferrites (CoFe_2O_4) nanoparticles were implanted into the ordered mesoporous cobaltosic oxide (Co_3O_4) nanowires to synthesize magnetic CoFe_2O_4/Co_3O_4 nanocomposites. X-ray diffraction (XRD), N_2 physical absorption–desorption, transmission electron microscope (TEM) and energy disperse spectroscopy (EDS) were used to characterize the microstructure of mesoporous Co_3O_4 and CoFe_2O_4/Co_3O_4 nanocomposites. The percent of pore-volume of mesoporous Co_3O_4 nanowires was calculated to be about 41.99% and CoFe_2O_4 nanoparticles were revealed to exist in the mesopores of Co_3O_4_. The magnetic behavior of both samples were investigated with superconducting quantum interference device (SQUID). Magnetization increased with the doping CoFe_2O_4 and decreasing temperature, while coercivity hardly changed. The exchange bias effect was obviously observed at 100 K and enhanced with the doping CoFe_2O_4. CoFe_2O_4 nanoparticles reinforced the interfaces magnetic interaction between antiferromagnetic Co_3O_4 and ferrimagnetic CoFe_2O_4.

Influence of gamma-radiation on percolation threshold in PE/α-Fe2O3 composite system

International Nuclear Information System (INIS)

Aliyev, N.S.; Bayramov, M.N.

2014-01-01

Full text : In this work it has been studied the change of specific volume resistance and also percolation threshold shift of the samples exposed to initial and gamma-irradiation depending on volume share of the filler α-Fe 2 O 3 in PE/α-Fe 2 O 3 composite. On the other hand while the volume share of the filler increases, the dimensions of polymer layer decreases on the border between phases

Structural and optical properties of cobalt doped multiferroics BiFeO3 nanostructure thin films

Science.gov (United States)

Prasannakumara, R.; Naik, K. Gopalakrishna

2018-05-01

Bismuth ferrite (BiFeO3) and Cobalt doped BiFeO3 (BiFe1-XCoXO3) nanostructure thin films were deposited on glass substrates by the sol-gel spin coating method. The X-ray diffraction patterns (XRD) of the grown BiFeO3 and BiFe1-XCoXO3 nanostructure thin films showed distorted rhombohedral structure. The shifting of peaks to higher angles was observed in cobalt doped BiFeO3. The surface morphology of the BiFeO3 and BiFe1-XCoXO3 nanostructure thin films were studied using FESEM, an increase in grain size was observed as Co concentration increases. The thickness of the nanostructure thin films was examined using FESEM cross-section. The EDX studies confirmed the elemental composition of the grown BiFeO3 and BiFe1-XCoXO3 nanostructure thin films. The optical characterizations of the grown nanostructure thin films were carried out using FTIR, it confirms the existence of Fe-O and Bi-O bands and UV-Visible spectroscopy shows the increase in optical band gap of the BiFeO3 nanostructure thin films with Co doping by ploting Tauc plot.

Synthesis and characterization of hollow α-Fe2O3 sub-micron spheres prepared by sol–gel

International Nuclear Information System (INIS)

León, Lizbet; Bustamante, Angel; Osorio, Ana; Olarte, G. S.; Santos Valladares, Luis De Los; Barnes, Crispin H. W.; Majima, Yutaka

2011-01-01

In this work we report the preparation of magnetic hematite hollow sub-micron spheres (α-Fe 2 O 3 ) by colloidal suspensions of ferric nitrate nine-hydrate (Fe(NO 3 ) 3 ·9H 2 O) particles in citric acid solution by following the sol–gel method. After the gel formation, the samples were annealed at different temperatures in an oxidizing atmosphere. Annealing at 180°C resulted in an amorphous phase, without iron oxide formation. Annealing at 250°C resulted in coexisting phases of hematite, maghemite and magnetite, whereas at 400°C, only hematite and maghemite were found. Pure hematite hollow sub-micron spheres with porous shells were formed after annealing at 600°C. The characterization was performed by X-ray diffraction (XRD), Mössbauer spectroscopy (MS) and scanning electron microscopy (SEM).

Hierarchically porous MnO2 microspheres doped with homogeneously distributed Fe3O4 nanoparticles for supercapacitors.

Science.gov (United States)

Zhu, Jian; Tang, Shaochun; Xie, Hao; Dai, Yuming; Meng, Xiangkang

2014-10-22

Hierarchically porous yet densely packed MnO2 microspheres doped with Fe3O4 nanoparticles are synthesized via a one-step and low-cost ultrasound assisted method. The scalable synthesis is based on Fe(2+) and ultrasound assisted nucleation and growth at a constant temperature in a range of 25-70 °C. Single-crystalline Fe3O4 particles of 3-5 nm in diameter are homogeneously distributed throughout the spheres and none are on the surface. A systematic optimization of reaction parameters results in isolated, porous, and uniform Fe3O4-MnO2 composite spheres. The spheres' average diameter is dependent on the temperature, and thus is controllable in a range of 0.7-1.28 μm. The involved growth mechanism is discussed. The specific capacitance is optimized at an Fe/Mn atomic ratio of r = 0.075 to be 448 F/g at a scan rate of 5 mV/s, which is nearly 1.5 times that of the extremely high reported value for MnO2 nanostructures (309 F/g). Especially, such a structure allows significantly improved stability at high charging rates. The composite has a capacitance of 367.4 F/g at a high scan rate of 100 mV/s, which is 82% of that at 5 mV/s. Also, it has an excellent cycling performance with a capacitance retention of 76% after 5000 charge/discharge cycles at 5 A/g.

Al/Fe isomorphic substitution versus Fe{sub 2}O{sub 3} clusters formation in Fe-doped aluminosilicate nanotubes (imogolite)

Energy Technology Data Exchange (ETDEWEB)

Shafia, Ehsan [Politecnico di Torino, Department of Applied Science and Technology and INSTM Unit of Torino-Politecnico (Italy); Esposito, Serena [Università degli Studi di Cassino e del Lazio Meridionale, Department of Civil and Mechanical Engineering (Italy); Manzoli, Maela; Chiesa, Mario [Università di Torino, Dipartimento di Chimica and Centro Interdipartimentale NIS (Italy); Tiberto, Paola [Electromagnetism, I.N.Ri.M. (Italy); Barrera, Gabriele [Università di Torino, Dipartimento di Chimica and Centro Interdipartimentale NIS (Italy); Menard, Gabriel [Harvard University, Department of Chemistry and Chemical Biology (United States); Allia, Paolo, E-mail: paolo.allia@polito.it [Politecnico di Torino, Department of Applied Science and Technology and INSTM Unit of Torino-Politecnico (Italy); Freyria, Francesca S. [Massachusetts Institute of Technology, Department of Chemistry (United States); Garrone, Edoardo; Bonelli, Barbara, E-mail: barbara.bonelli@polito.it [Politecnico di Torino, Department of Applied Science and Technology and INSTM Unit of Torino-Politecnico (Italy)

2015-08-15

Textural, magnetic and spectroscopic properties are reported of Fe-doped aluminosilicate nanotubes (NTs) of the imogolite type, IMO, with nominal composition (OH){sub 3}Al{sub 2−x}Fe{sub x}O{sub 3}SiOH (x = 0, 0.025, 0.050). Samples were obtained by either direct synthesis (Fe-0.025-IMO, Fe-0.050-IMO) or post-synthesis loading (Fe-L-IMO). The Fe content was either 1.4 wt% (both Fe-0.050-IMO and Fe-L-IMO) or 0.7 wt% (Fe-0.025-IMO). Textural properties were characterized by High-Resolution Transmission Electron Microscopy, X-ray diffraction and N{sub 2} adsorption/desorption isotherms at 77 K. The presence of different iron species was studied by magnetic moment measurements and three spectroscopies: Mössbauer, UV–Vis and electron paramagnetic resonance, respectively. Fe{sup 3+}/Al{sup 3+} isomorphic substitution (IS) at octahedral sites at the external surface of NTs is the main process occurring by direct synthesis at low Fe loadings, giving rise to the formation of isolated high-spin Fe{sup 3+} sites. Higher loadings give rise, besides IS, to the formation of Fe{sub 2}O{sub 3} clusters. IS occurs up to a limit of Al/Fe atomic ratio of ca. 60 (corresponding to x = 0.032). A fraction of the magnetism related to NCs is pinned by the surface anisotropy; also, clusters are magnetically interacting with each other. Post-synthesis loading leads to a system rather close to that obtained by direct synthesis, involving both IS and cluster formations. Slightly larger clusters than with direct synthesis samples, however, are formed. The occurrence of IS indicates a facile cleavage/sealing of Al–O–Al bonds: this opens the possibility to exchange Al{sup 3+} ions in pre-formed IMO NTs, a much simpler procedure compared with direct synthesis.

First-principles investigation of Fe-doped MgSiO3-ilmenite

International Nuclear Information System (INIS)

Stashans, Arvids; Rivera, Krupskaya; Pinto, Henry P.

2012-01-01

First principles density functional theory and generalised gradient approximation (GGA) have been exploited to investigate Fe-doped ilmenite-type MgSiO 3 mineral. Strong electron correlation effects not included in a density-functional formalism are described by a Hubbard-type on-site Coulomb repulsion (the DFT+U approach). Microstructure of equilibrium geometries, electronic band structures as well as magnetic properties are computed and discussed in detail. Hartree-Fock methodology is used as an extra tool to study optical properties of the same system. For equilibrium state of the doped mineral we find zigzag-type atomic rearrangements around the Fe impurity. The inclusion of correlation effects leads to an improved description of the electronic properties. In particular, it is discovered that Fe incorporation produces local energy levels within the band-gap of the material. Using ΔSCF method optical absorption energies are found to be equal to 2.2 and 2.6 eV leading to light absorption at longer wavelengths compared to the undoped MgSiO 3 . Our results provide evidence on the occurrence of local magnetic moment in the region surrounding iron dopant. According to the outcomes, the Fe⇒Mg reaction can be described as substitutionally labile with Fe 2+ complex being found in the high-spin state at low pressure MgSiO 3 -ilmenite conditions.

Synthesis of Ce(III)-doped Fe3O4 magnetic particles for efficient removal of antimony from aqueous solution

International Nuclear Information System (INIS)

Qi, Zenglu; Joshi, Tista Prasai; Liu, Ruiping; Liu, Huijuan; Qu, Jiuhui

2017-01-01

Highlights: • Doping of Ce into Fe 3 O 4 was achieved based on a facile solvothermal method. • After doping, the removal capacity was increased by 5 times for “Sb(V)” and 2 times for “Sb(III)”. • Decreasing pH improved adsorption of Sb(V) but decreased adsorption of Sb(III). • Antimony sorption mechanisms on Ce-doped Fe 3 O 4 were illustrated. - Abstract: Aqueous antimony (Sb) pollution from human activity is of great concern in drinking water due to its adverse health effect. Magnetic Fe 3 O 4 particles, with high separation ability from solution, have been considered as a low-cost Sb adsorbent for contaminants. However, the limited adsorption capacity has restricted its practical application. In this study, a solvothermal approach was developed for doping Ce(III) into Fe 3 O 4 , thereby increasing the adsorption efficacy for both Sb(III) and Sb(V). In contrast to un-doped Fe 3 O 4 , the adsorption capacity towards Sb(III) and Sb(V) in Ce-doped materials increased from 111.4 to 224.2 mg/g and from 37.2 to 188.1 mg/g at neutral pH, respectively. Based on the combined results of XPS, XRD, and FTIR, it confirmed that Ce atom successfully doped into the Fe 3 O 4 structure, resulting in the decreased particle size, increased the surface area, and isoelectric point. Furthermore, the vibrating sample magnetometer (VSM) results showed that the Ce doping process had some side effects on the primitive magnetic property, but remaining the high separation potential during water treatment. According to the high removal efficiency and magnetic property, the Ce-doped Fe 3 O 4 of great simplicity should be a promising adsorbent for aqueous Sb removal.

Structural, optical, and magnetic properties of Mn and Fe-doped Co3O4 nanoparticles

Directory of Open Access Journals (Sweden)

C. Stella

2015-08-01

Full Text Available Mn and Fe-doped Co3O4 nanoparticles were prepared by a simple precipitation method. The synthesized particles were characterized by X-ray diffraction (XRD, scanning electron microscope (SEM, transmission electron microscope (TEM, UV-Vis absorption spectroscopy, Fourier transform infrared spectroscopy (FTIR, Raman spectroscopy, and vibrating sample magnetometer (VSM techniques. XRD analysis showed the cubic structure of Co3O4. SEM and TEM images confirmed the formation of interconnected nanoparticles. Mn and Fe-doped Co3O4 showed broad absorption in the visible region compared to undoped sample and the band gap values are red shifted. Five Raman active modes were observed from the Raman spectra. FTIR spectra confirmed the spinel structure of Co3O4 and the doping of Mn and Fe shifts the vibrational modes to lower wave number region. The magnetic measurements confirmed that Fe-doped Co3O4 shows a little ferromagnetic behavior compared to undoped and Mn-doped Co3O4, which could be related to the uncompensated surface spins and the finite size effects.

Facile synthesis of Sm-doped BiFeO{sub 3} nanoparticles for enhanced visible light photocatalytic performance

Energy Technology Data Exchange (ETDEWEB)

Hu, Zijun; Chen, Da, E-mail: dchen_80@hotmail.com; Wang, Sen; Zhang, Ning; Qin, Laishun, E-mail: qinlaishun@cjlu.edu.cn; Huang, Yuexiang

2017-06-15

Highlights: • Effective Sm doping into BiFeO{sub 3} nanoparticles was obtained by a facile sol-gel route. • Band gap of Sm-doped BiFeO{sub 3} nanoparticles was regulated by the dopant concentration. • Sm-doped BiFeO{sub 3} nanoparticles exhibited superior photocatalytic activities. • The possible photocatalytic mechanism of Sm-doped BiFeO{sub 3} nanospheres was discussed. - Abstract: In this work, the effect of Sm doping on the structural and photocatalytic properties of BiFeO{sub 3} (BFO) was investigated. A series of Sm doped BFO nanoparticles containing different Sm dopant contents (Bi{sub (1−x)}Sm{sub x}FeO{sub 3}, x = 0.00, 0.01, 0.03, 0.05, 0.07, 0.10) were synthesized via a simple sol-gel route. It was revealed that Sm{sup 3+} ions were successfully doped into BFO nanoparticles, and the band gap value was gradually decreased when increasing Sm dopant concentration. The photocatalytic activity of Sm-doped BFO photocatalyst was significantly affected by the Sm doping content. Compared to pure BFO, the Sm-doped BFO samples exhibited much higher photocatalytic activity. The improved photocatalytic activity of Sm-doped BFO could be attributed to the enhanced visible light absorption and the efficient separation of photogenerated electrons and holes derived from Sm dopant trapping level in the Sm-doped BFO samples. In addition, the possible photocatalytic mechanism of Sm-doped BFO photocatalyst was also proposed.

3d-metal doping (Fe,Co,Ni,Zn) of the high Tc perovskite YBa2Cu3O(7-y)

International Nuclear Information System (INIS)

Tarascon, J.M.; Barboux, P.; Greene, L.H.; Hull, G.W.; Bagley, B.G.

1988-01-01

The structural, magnetic and superconducting properties of the mixed compounds YBa 2 Cu(3-x)M(x)O(7-y) (M = Ni,Zn,Fe, and Co) are reported. Values of y, determined by titration, are found to be dependent on the nature and amount of the doping. The range of solubility is greater for the Fe and Co compounds (x = 1) than for those with Ni or Zn (x = 0.3). The undoped material is orthorhombic and remains orthorhombic after substitution for Cu by Ni or Zn, whereas a tetragonal phase is observed when Fe, Co are substituted for Cu. DC resistance and AC susceptibility measurements show that Tc is depressed from 90K (x = 0) to 45K (x = 0.2) for both the Ni- and Zn-doped compounds, and Tc is destroyed in the Fe- and Co-doped compounds when x reaches 0.4. It is suggested that a valence of two be assigned to the Ni and Zn and three to the Fe and Co ions. 8 references

First-principles investigation of Fe-doped MgSiO{sub 3}-ilmenite

Energy Technology Data Exchange (ETDEWEB)

Stashans, Arvids, E-mail: arvids@utpl.edu.ec [Grupo de Fisicoquimica de Materiales, Universidad Tecnica Particular de Loja, Apartado 11-01-608, Loja (Ecuador); Rivera, Krupskaya [Grupo de Fisicoquimica de Materiales, Universidad Tecnica Particular de Loja, Apartado 11-01-608, Loja (Ecuador); Escuela de Geologia y Minas, Universidad Tecnica Particular de Loja, Apartado 11-01-608, Loja (Ecuador); Pinto, Henry P. [Interdisciplinary Center for Nanotoxicity, Department of Chemistry, Jackson State University, Jackson, Mississippi 39217-0510 (United States)

2012-06-15

First principles density functional theory and generalised gradient approximation (GGA) have been exploited to investigate Fe-doped ilmenite-type MgSiO{sub 3} mineral. Strong electron correlation effects not included in a density-functional formalism are described by a Hubbard-type on-site Coulomb repulsion (the DFT+U approach). Microstructure of equilibrium geometries, electronic band structures as well as magnetic properties are computed and discussed in detail. Hartree-Fock methodology is used as an extra tool to study optical properties of the same system. For equilibrium state of the doped mineral we find zigzag-type atomic rearrangements around the Fe impurity. The inclusion of correlation effects leads to an improved description of the electronic properties. In particular, it is discovered that Fe incorporation produces local energy levels within the band-gap of the material. Using {Delta}SCF method optical absorption energies are found to be equal to 2.2 and 2.6 eV leading to light absorption at longer wavelengths compared to the undoped MgSiO{sub 3}. Our results provide evidence on the occurrence of local magnetic moment in the region surrounding iron dopant. According to the outcomes, the Fe Rightwards-Double-Arrow Mg reaction can be described as substitutionally labile with Fe{sup 2+} complex being found in the high-spin state at low pressure MgSiO{sub 3}-ilmenite conditions.

Quasicubic α-Fe{sub 2}O{sub 3} nanoparticles embedded in TiO{sub 2} thin films grown by atomic layer deposition

Energy Technology Data Exchange (ETDEWEB)

Tamm, Aile [Institute of Physics, University of Tartu, W. Ostwaldi 1, 50411 Tartu (Estonia); Seinberg, Liis [National Institute of Chemical Physics and Biophysics, Akadeemia tee 23, 12618 Tallinn (Estonia); Kozlova, Jekaterina [Institute of Physics, University of Tartu, W. Ostwaldi 1, 50411 Tartu (Estonia); Link, Joosep [National Institute of Chemical Physics and Biophysics, Akadeemia tee 23, 12618 Tallinn (Estonia); Pikma, Piret [University of Tartu, Institute of Chemistry, Ravila 14A, 50411 Tartu (Estonia); Stern, Raivo [National Institute of Chemical Physics and Biophysics, Akadeemia tee 23, 12618 Tallinn (Estonia); Kukli, Kaupo [Institute of Physics, University of Tartu, W. Ostwaldi 1, 50411 Tartu (Estonia); Department of Chemistry, University of Helsinki, P.O. Box 55, FI-00014 Helsinki (Finland)

2016-08-01

Monodispersed quasicubic α-Fe{sub 2}O{sub 3} nanoparticles were synthesized from ferric nitrite (Fe(NO{sub 3}){sub 3}), N,N-dimethyl formamide and poly(N-vinyl-2-pyrrolidone). Layers of nanoparticles were attached to HF-etched Si substrates by dip coating and subsequently embedded in thin titanium oxide films grown by atomic layer deposition from TiCl{sub 4} and H{sub 2}O. The deposition of TiO{sub 2} onto Fe{sub 2}O{sub 3} nanoparticles covered the nanoparticles uniformly and anatase phase of TiO{sub 2} was observed in Si/Fe{sub 2}O{sub 3}/TiO{sub 2} nanostructures. In Si/Fe{sub 2}O{sub 3}/TiO{sub 2} nanostructure magnetic domains, observable by magnetic force microscopy, were formed and these nanostructures implied ferromagnetic-like behavior at room temperature with the saturative magnetization and coercivity of 10 kA/m. - Highlights: • Cubic-shaped iron oxide crystallites were supported by thin titanium oxide films. • The process chemistry applied allowed formation of heterogeneous composite. • Atomic layer deposition of titanium oxide on nanocubes was uniform and conformal. • The nanostructures formed can be regarded as magnetically susceptible materials.

Structural, magnetic, and electrical properties of Gd-doped BiFeO3 nanoparticles with reduced particle size

International Nuclear Information System (INIS)

Lotey, Gurmeet Singh; Verma, N. K.

2012-01-01

Pure and Gd-doped BiFeO 3 nanoparticles have been synthesized by sol–gel method. The significant effects of size and Gd-doping on structural, electrical, and magnetic properties have been investigated. X-ray diffraction study reveals that the pure BiFeO 3 nanoparticles possess rhombohedral structure, but with 10% Gd-doping complete structural transformation from rhombohedral to orthorhombic has been observed. The particle size of pure and Gd-doped BiFeO 3 nanoparticles, calculated using Transmission electron microscopy, has been found to be in the range 25–15 nm. Pure and Gd-doped BiFeO 3 nanoparticles show ferromagnetic character, and the magnetization increases with decrease in particle size and increase in doping concentration. Scanning electron microscopy study reveals that grain size decreases with increase in Gd concentration. Well-saturated polarization versus electric field loop is observed for the doped samples. Leakage current density decreases by four orders by doping Gd in BiFeO 3 . The incorporation of Gd in BiFeO 3 enhances spin as well as electric polarization at room temperature. The possible origin of enhancement in these properties has been explained on the basis of dopant and its concentration, phase purity, small particle, and grain size.

Boundary structure modification and magnetic properties of Nd-Fe-B sintered magnets by co-doping with Dy{sub 2}O{sub 3}/S powders

Energy Technology Data Exchange (ETDEWEB)

Yang, Fang [Institute for Advanced Materials& Technology, University of Science and Technology Beijing, Beijing 100083 (China); Guo, Leichen [School of Engineering Technology, Purdue University, West Lafayette, Indiana 47907 (United States); Li, Ping [Institute for Advanced Materials& Technology, University of Science and Technology Beijing, Beijing 100083 (China); Zhao, Xuzhe [School of Engineering Technology, Purdue University, West Lafayette, Indiana 47907 (United States); Sui, Yanli [State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing 100083 (China); Guo, Zhimeng, E-mail: guozhimengustb@163.com [Institute for Advanced Materials& Technology, University of Science and Technology Beijing, Beijing 100083 (China); Gao, Xuexu [State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing 100083 (China)

2017-05-01

In this paper, the effect of Dy{sub 2}O{sub 3}/S co-doping on the magnetic properties and microstructure was studied in Nd-Fe-B sintered magnets. With S co-doping, the coercivity increased due to grain boundary modification and Dy selective introduction. Continuous grain boundary phases were formed in the co-doped magnets with smaller grain size. The average grain size after a doping of 0.2 wt% S is 7.25 µm, which is approximately 2.37 µm smaller than that of the S-free sintered magnets(9.62 µm). The coercivity of the Dy{sub 2}O{sub 3}/0.2 wt% S co-doped magnets could be increased from 20.9 to 22.8 kOe with changing the remanence and the maximum magnetic energy product slightly. S precipitates in the Nd-rich phases were hexagonal Nd{sub 2}O{sub 2}S phase. Dy avoided the Nd{sub 2}O{sub 2}S phase in the triple junction region, resulting in more available Dy atoms diffusing into the Nd{sub 2}Fe{sub 14}B phase grains to enhance the anisotropy field. Dy-saving was achieved by forming Nd{sub 2}O{sub 2}S phase in the Dy{sub 2}O{sub 3}/S co-doped magnets. - Highlights: • The average grain size of Dy{sub 2}O{sub 3}/S co-doped magnets is 2.37 μm smaller than that of Dy{sub 2}O{sub 3} doped magnets. • The Dy atoms avoid the Nd{sub 2}O{sub 2}S phases and more of them become available to diffuse into the Nd{sub 2}Fe{sub 14}B phases. • The coercivity reaches maximum when S content is 0.2 wt%, 9% higher than the 20.9 kOe coercivity of the S-free magnets.

Study of cerium doped magnetite (Fe 3O 4:Ce)/PMMA nanocomposites

Science.gov (United States)

Padalia, Diwakar; Johri, U. C.; Zaidi, M. G. H.

2012-03-01

The paper presents the synthesis and properties of polymer nanocomposite material based on cerium doped magnetite (Fe 3O 4) as filler material and poly methyl methacrylate (PMMA) as host matrix. The magnetite (Fe 3O 4) particles were synthesized by co-precipitation route using stable ferrous and ferric salts with ammonium hydroxide as precipitating agent. Further, they doped by cerium oxide (CeO 2) non-stoichiometrically. The composite material was fabricated by solvent evaporation method. Here 2.4 GHz microwaves were used to study the effect of microwaves heating on polymerization. The phase and crystal structure is determined by X-ray diffraction (XRD). The average crystallite size of the composites varies from 28 to 35 nm. The chemical structure is confirmed by Fourier transform infrared (FTIR) spectroscopy. The magnetic and thermal properties are investigated by vibrating sample magnetometer (VSM) and differential scanning calorimetry (DSC). The thermal study shows that the microwave heated samples possess higher glass transition temperature ( Tg). The magnetic results suggest that coercivity ( HC) and squareness ( Mr/ Ms) of the loop increases with increasing doping percent of cerium.

Nanoscale TiO2 and Fe2O3 Architectures for Solar Energy Conversion Schemes

Science.gov (United States)

Sedach, Pavel Anatolyvich

The direct conversion of sunlight into more useable forms of energy has the potential of alleviating the environmental and social problems associated with a dependence on fossil fuels. If solar energy is to be utilized en-masse, however, it must be inexpensive and widely available. In this vein, the focus of this thesis is on nanostructured materials relevant to solar energy conversion and storage. Specifically, this thesis describes the ambient sol-gel synthesis of titanium dioxide (Ti02) nanowires designed for enhanced charge-transfer in solar collection devices, and the synthesis of novel disordered metal-oxide (MOx) catalysts for water oxidation. The introductory chapter of this thesis gives an overview of the various approaches to solar energy conversion. Sol---gel reaction conditions that enable the growth of one-dimensional (1-D) anatase TiO2 nanostructures from fluorine-doped tin oxide (FTO) for photovoltaics (PVs) are described in the second chapter. The generation of these linear nanostructures in the absence of an external bias or template is achieved by using facile experimental conditions (e.g., acetic acid (HOAc) and titanium isopropoxide (Ti(OiPr)4) in anhydrous heptane). The procedure was developed by functionalizing base-treated substrates with Ti-oxide nucleation sites that serve as a foundation for the growth of linear Ti-oxide macromolecules, which upon calcination, render uniform films of randomly oriented anatase TiO2 nanowires. A systematic evaluation of how reaction conditions (e.g., solvent volume, stoichiometry of reagents, substrate base treatment) affect the generation of these TiO 2 films is presented. A photo-organic MO. deposition route (i.e., photochemical metal-organic deposition (PMOD)) used to deposit thin-films of amorphous iron oxide (a-Fe2O3) for water oxidation catalysis is detailed in third chapter. It is shown that the irradiation of a spin-coated metal-organic film produces a film of non-crystalline a-Fe203. It is shown

Mg shallow doping effects on the ac magnetic self-heating characteristics of γ-Fe2O3 superparamagnetic nanoparticles for highly efficient hyperthermia

Science.gov (United States)

Jang, Jung-tak; Bae, Seongtae

2017-10-01

The effects of Mg doping on the magnetic and AC self-heating temperature rising characteristics of γ-Fe2O3 superparamagnetic nanoparticles (SPNPs) were investigated for hyperthermia applications in biomedicine. The doping concentration of nonmagnetic Mg2+ cation was systematically controlled from 0 to 0.15 at. % in Mgx-γFe2O3 SPNPs during chemically and thermally modified one-pot thermal decomposition synthesis under bubbling O2/Ar gas mixture. It was empirically observed that the saturation magnetization (Ms) and the out-of-phase magnetic susceptibility ( χm″)of Mgx-γFe2O3 SPNPs were increased by increasing the Mg2+ cation doping concentration from 0.05 to 0.13 at. %. Correspondingly, the AC magnetically induced self-heating temperature (Tac,max) in solid state and the intrinsic loss power in water were increased up to 184 °C and 14.2 nH m2 kg-1 (Mgx-γFe2O3, x = 0.13), respectively, at the biologically and physiologically safe range of AC magnetic field (Happl × fappl = 1.2 × 109 A m-1 s-1). All the chemically and physically analyzed results confirmed that the dramatically improved AC magnetic induction heating characteristics and the magnetic properties of Mgx-γFe2O3 SPNPs (x = 0.13) are primarily due to the significantly enhanced magnetic susceptibility (particularly, χm″) and the improved AC/DC magnetic softness (lower AC/DC magnetic anisotropy) resulting from the systematically controlled nonmagnetic Mg2+ cation concentrations and distributions (occupation ratio) in the Fe vacancy sites of γ-Fe2O3 (approximately 12% vacancy), instead of typically well-known Fe3O4 (no vacancy) SPNPs. The cell viability and biocompatibility with U87 MG cell lines demonstrated that Mgx-γFe2O3 SPNPs (x = 0.13) has promising bio-feasibility for hyperthermia agent applications.

Facile synthesis of Fe4N/Fe2O3/Fe/porous N-doped carbon nanosheet as high-performance anode for lithium-ion batteries

Science.gov (United States)

Zhang, Dan; Li, Guangshe; Yu, Meijie; Fan, Jianming; Li, Baoyun; Li, Liping

2018-04-01

Iron nitrides are considered as highly promising anode materials for lithium-ion batteries because of their nontoxicity, high abundance, low cost, and higher electrical conductivity. Unfortunately, their limited synthesis routes are available and practical application is still hindered by their fast capacity decay. Herein, a facile and green route is developed to synthesize Fe4N/Fe2O3/Fe/porous N-doped carbon nanosheet composite. The size of Fe4N/Fe2O3/Fe particles is small (10-40 nm) and they are confined in porous N-doped carbon nanosheet. These features are conducive to accommodate volume change well, shorten the diffusion distance and further elevate electrical conductivity. When tested as anode material for lithium-ion batteries, a high discharge capacity of 554 mA h g-1 after 100 cycles at 100 mA g-1 and 389 mA h g-1 after 300 cycles at 1000 mA g-1 are retained. Even at 2000 mA g-1, a high capacity of 330 mA h g-1 can be achieved, demonstrating superior cycling stability and rate performance. New prospects will be brought by this work for the synthesis and the potential application of iron nitrides materials as an anode for LIBs.

Tunable flux pinning landscapes achieved by functional ferromagnetic Fe2O3:CeO2 vertically aligned nanocomposites in YBa2Cu3O7−δ thin films

International Nuclear Information System (INIS)

Tsai, Chen-Fong; Huang, Jijie; Lee, Joon-Hwan; Khatkhatay, Fauzia; Chen, Li; Chen, Aiping; Su, Qing; Wang, Haiyan

2015-01-01

Highlights: • Functional ferromagnetic (Fe 2 O 3 ) x :(CeO 2 ) 1−x vertically aligned nanocomposites (VAN). • An ordered arrangement of ferromagnetic Fe 2 O 3 nanoinclusions. • Significant in-field improvement of J c (H//c) in both VAN nanolayer capped and buffered samples. • T c above 90 K and the J c sf maximized at 3.07 MA/cm 2 (75 K) and 9.2 MA/cm 2 (65 K) for 30% Fe 2 O 3 sample. - Abstract: Functional ferromagnetic (Fe 2 O 3 ) x :(CeO 2 ) 1−x vertically aligned nanocomposite (VAN) layers were deposited as either buffer or cap layers for YBa 2 Cu 3 O 7−δ (YBCO) thin films. The composition of Fe 2 O 3 dopants in the VAN nanolayers is controlled at 10%, 30% and 50% in order to create different arrangements of Fe 2 O 3 and CeO 2 nanopillars and therefore to tune the flux pining landscapes. The composition variation provides tunable and ordered arrangements of magnetic nanodopants and interfacial defects as pinning centers in the YBCO thin films. The superconducting property measurements show that most doped samples obtain a T c above 90 K and the J c sf measured at 75 K and 65 K maximized at 3.07 MA/cm 2 and 9.2 MA/cm 2 for 30% Fe 2 O 3 VAN doped sample. As the temperature decreased to 5 K, the sample with 50% Fe 2 O 3 VAN doped sample show the best pinning effect due to pronounced magnetic pinning effects. This work demonstrates the tunable density of magnetic pinning centers can be achieved by VAN to meet the specific pinning requirement

Enhanced visible light photocatalytic properties of Fe-doped TiO2 nanorod clusters and monodispersed nanoparticles

International Nuclear Information System (INIS)

Liu, Y.; Wei, J.H.; Xiong, R.; Pan, C.X.; Shi, J.

2011-01-01

In order to get photocatalysts with desired morphologies and enhanced visible light responses, the Fe-doped TiO 2 nanorod clusters and monodispersed nanoparticles were prepared by modified hydrothermal and solvothermal method, respectively. The microstructures and morphologies of TiO 2 crystals can be controlled by restraining the hydrolytic reaction rates. The Fe-doped photocatalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV-vis absorption spectroscopy (UV-vis), N 2 adsorption-desorption measurement (BET), and photoluminescence spectroscopy (PL). The refinements of the microstructures and morphologies result in the enhancement of the specific surface areas. The Fe 3+ -dopants in TiO 2 lattices not only lead to the significantly extending of the optical responses from UV to visible region but also diminish the recombination rates of the electrons and holes. The photocatalytic activities were evaluated by photocatalytic decomposition of formaldehyde in air under visible light illumination. Compared with P25 (TiO 2 ) and N-doped TiO 2 nanoparticles, the Fe-doped photocatalysts show high photocatalytic activities under visible light.

Structural, Raman, and dielectric studies on multiferroic Mn-doped Bi 1-xLax FeO 3 ceramics

KAUST Repository

Xing, Zhibiao

2014-04-03

Multiferroic Bi1-xLaxFeO3 [BLFO (x)] ceramics with x = 0.10-0.50 and Mn-doped BLFO (x = 0.30) ceramics with different doping contents (0.1-1.0 mol%) were prepared by solid-state reaction method. They were crystallized in a perovskite phase with rhombohedral symmetry. In the BLFO (x) system, a composition (x)-driven structural transformation (R3c→C222) was observed at x = 0.30. The formation of Bi2Fe 4O9 impure phase was effectively suppressed with increasing the x value, and the rhombohedral distortion in the BLFO ceramics was decreased, leading to some Raman active modes disappeared. A significant red frequency shift (~13 cm-1) of the Raman mode of 232 cm-1 in the BLFO ceramics was observed, which strongly perceived a significant destabilization in the octahedral oxygen chains, and in turn affected the local FeO6 octahedral environment. In the Mn-doped BLFO (x = 0.30) ceramics, the intensity of the Raman mode near 628 cm-1 was increased with increasing the Mn-doping content, which was resulted from an enhanced local Jahn-Teller distortions of the (Mn,Fe)O6 octahedra. Electron microscopy images revealed some changes in the ceramic grain sizes and their morphologies in the Mn-doped samples at different contents. Wedge-shaped 71° ferroelectric domains with domain walls lying on the {110} planes were observed in the BLFO (x = 0.30) ceramics, whereas in the 1.0 mol% Mn-doped BLFO (x = 0.30) samples, 71° ferroelectric domains exhibited a parallel band-shaped morphology with average domain width of 95 nm. Dielectric studies revealed that high dielectric loss of the BLFO (x = 0.30) ceramics was drastically reduced from 0.8 to 0.01 (measured @ 104 Hz) via 1.0 mol% Mn-doping. The underlying mechanisms can be understood by a charge disproportion between the Mn4+ and Fe2+ in the Mn-doped samples, where a reaction of Mn4+ + Fe2+→Mn3+ + Fe3+ is taken place, resulting in the reduction in the oxygen vacancies and a suppression of the electron hopping from Fe3+ to Fe2+ ions

Structural, Raman, and dielectric studies on multiferroic Mn-doped Bi 1-xLax FeO 3 ceramics

KAUST Repository

Xing, Zhibiao; Zhu, Xinhua; Zhu, Jianmin; Liu, Zhiguo; Al-Kassab, Talaat

2014-01-01

Multiferroic Bi1-xLaxFeO3 [BLFO (x)] ceramics with x = 0.10-0.50 and Mn-doped BLFO (x = 0.30) ceramics with different doping contents (0.1-1.0 mol%) were prepared by solid-state reaction method. They were crystallized in a perovskite phase with rhombohedral symmetry. In the BLFO (x) system, a composition (x)-driven structural transformation (R3c→C222) was observed at x = 0.30. The formation of Bi2Fe 4O9 impure phase was effectively suppressed with increasing the x value, and the rhombohedral distortion in the BLFO ceramics was decreased, leading to some Raman active modes disappeared. A significant red frequency shift (~13 cm-1) of the Raman mode of 232 cm-1 in the BLFO ceramics was observed, which strongly perceived a significant destabilization in the octahedral oxygen chains, and in turn affected the local FeO6 octahedral environment. In the Mn-doped BLFO (x = 0.30) ceramics, the intensity of the Raman mode near 628 cm-1 was increased with increasing the Mn-doping content, which was resulted from an enhanced local Jahn-Teller distortions of the (Mn,Fe)O6 octahedra. Electron microscopy images revealed some changes in the ceramic grain sizes and their morphologies in the Mn-doped samples at different contents. Wedge-shaped 71° ferroelectric domains with domain walls lying on the {110} planes were observed in the BLFO (x = 0.30) ceramics, whereas in the 1.0 mol% Mn-doped BLFO (x = 0.30) samples, 71° ferroelectric domains exhibited a parallel band-shaped morphology with average domain width of 95 nm. Dielectric studies revealed that high dielectric loss of the BLFO (x = 0.30) ceramics was drastically reduced from 0.8 to 0.01 (measured @ 104 Hz) via 1.0 mol% Mn-doping. The underlying mechanisms can be understood by a charge disproportion between the Mn4+ and Fe2+ in the Mn-doped samples, where a reaction of Mn4+ + Fe2+→Mn3+ + Fe3+ is taken place, resulting in the reduction in the oxygen vacancies and a suppression of the electron hopping from Fe3+ to Fe2+ ions

Enhanced magnetic and ferroelectric properties in scandium doped nano Bi{sub 2}Fe{sub 4}O{sub 9}

Energy Technology Data Exchange (ETDEWEB)

Dutta, Dimple P., E-mail: dimpled@barc.gov.in [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Sudakar, C.; Mocherla, Pavana S.V. [Department of Physics, IIT Madras, Chennai 600 036 (India); Mandal, Balaji P.; Jayakumar, Onnatu D. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Tyagi, Avesh K., E-mail: aktyagi@barc.gov.in [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)

2012-08-15

In this study we report the synthesis of undoped and Sc{sup 3+} doped Bi{sub 2}Fe{sub 4}O{sub 9} nanoparticles using sonochemical technique. X-ray diffraction reveals that all samples are single phase with no impurities detected. EDS analysis was done to confirm the extent of Sc{sup 3+} doping in the samples. The size and morphology of the nanoparticles have been analyzed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The Bi{sub 2}Fe{sub 4}O{sub 9} nanoparticles show a weak ferromagnetic behavior at room temperature, which is quite different from the linear M-H relationship reported for bulk Bi{sub 2}Fe{sub 4}O{sub 9}. A magnetization of 0.144 {mu}B/f.u. is obtained at 300 K, which is mainly attributed to the uncompensated moments at the disordered particle surface resulting from the reduced coordination of the surface spins, arising due to lattice strain or oxygen deficiency. Addition of Sc{sup 3+} dopant in varying concentrations in these Bi{sub 2}Fe{sub 4}O{sub 9} nanoparticles, improves their magnetic as well as ferroelectric properties. The leakage current is considerably reduced and electric polarization increases significantly in case of Bi{sub 2}Fe{sub 4(1-x)}Sc{sub x}O{sub 9} (x = 0.1) nanoparticles. Thus it can be inferred that Sc{sup 3+} doped Bi{sub 2}Fe{sub 4}O{sub 9} nanoparticles shows promise as good multiferroic materials. -- Graphical abstract: Undoped and Sc{sup 3+} doped Bi{sub 2}Fe{sub 4}O{sub 9} nanoparticles have been synthesized using sonochemical technique. The bi-functionalities of Sc{sup 3+} doped Bi{sub 2}Fe{sub 4}O{sub 9} nanoparticles have been demonstrated. The Bi{sub 2}Fe{sub 4(1-x)}Sc{sub x}O{sub 9} (x = 0.1) nanoparticles showed enhanced magnetic and ferroelectric properties with considerably less lossy characteristics compared to the bulk Bi{sub 2}Fe{sub 4}O{sub 9}. Highlights: Black-Right-Pointing-Pointer Phase pure Bi{sub 2}Fe{sub 4}O{sub 9} nanostructures synthesized using a facile

On the synthesis, characterization, rationalization of the structure and the compositional formula of Ti-substituted Li0,5Fe2,5O4

International Nuclear Information System (INIS)

Widatallah, H.M.; Berry, F.J.; Moore, E.A.; Johnson, C.; Jartych, E.; Pekala, M.; Grabski, J.

2002-12-01

Spinel-related titanium-substituted Li 0.5 Fe 2.5 O 4 has been synthesised by heating a mixture of titanium-doped corundum-related α-Fe 2 O 3 with Li 2 CO 3 at 850 deg C which is ca. 250-350 deg C lower than temperatures at which the material is normally prepared conventionally. Moessbauer and magnetic measurements imply that the Ti 4+ ions substitute for octahedral Fe 3+ ions. Interatomic potential calculations support this substitution with the charge balance being maintained by Li + vacancies. This structural model leads to a compositional formula of the type Li (0.5-x) + Ti x 4+ Fe (2.5-x) 3+ O 4 which is shown to be more appropriate than the one generally used in the literature, namely Li (0.5+0.5x) + Ti x 4+ Fe (2.5-1.5x) 3+ O 4 . Some implications of the suggested formula are discussed including the possibility of the existence of a thermodynamically stable titanium ferrite of the form Ti 0.5 Fe 2 O 4 . (author)

Spectroscopic and dielectric properties of titanium doped MgO-Al{sub 2}O{sub 3}-B{sub 2}O{sub 3} glass system

Energy Technology Data Exchange (ETDEWEB)

Raju, G Naga; Ramesh, N Ch; Naresh, P; Krishna, T L; Srinivasulu, K; Sudhkar, K S V; Rao, P Venkateswara, E-mail: gnag_9@rediffmail.com [Department of Physics, Acharya Nagarjuna University-Nuzvid Campus, Nuzvid - 521 201 (India)

2009-07-15

In this paper we have reported the influence of titanium ions on different spectroscopic and dielectric properties of MgO-Al{sub 2}O{sub 3}-B{sub 2}O{sub 3} glasses. The analysis of result of all these studies has indicated that as the concentration of TiO{sub 2} increased in the glass matrix, there is a gradual transformation of titanium ions from octahedral position to tetrahedral positions and cause to increase the rigidity of glass network.

SYNTHESIS OF MAGNETIC NANOPARTICLES OF TiO2-NiFe2O4: CHARACTERIZATION AND PHOTOCATALYTIC ACTIVITY ON DEGRADATION OF RHODAMINE B

Directory of Open Access Journals (Sweden)

Rahmayeni Rahmayeni

2012-12-01

Full Text Available Magnetic nanoparticles of TiO2-(xNiFe2O4 with x = 0.01, 0.1, and 0.3have been synthesized by mixture of titanium isopropoxide (TIP and nitric metal as precursors. The particles were characterized by XRD, SEM-EDX, and VSM. XRD pattern show the peaks at 2q = 25.3°, 38.4° and 47.9° which are referred as anatase phase of TiO2. Meanwhile NiFe2O4 phase was observed clearly for x = 0.3. The present of NiFe2O4 can prevent the transformation of TiO2 from anatase to rutile when the calcination temperature increased. Microstructure analyses by SEM show the homogeneous form and size of particles. The magnetic properties analysis by VSM indicates that TiO2-NiFe2O4 is paramagnetic behavior. TiO2 doped NiFe2O4 has higher photocatalytic activity than TiO2 synthesized for degradation of Rhodamine B in aqueous solution under solar light irradiation.

Synthesis of Ce(III)-doped Fe{sub 3}O{sub 4} magnetic particles for efficient removal of antimony from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Qi, Zenglu; Joshi, Tista Prasai [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Ruiping, E-mail: liuruiping@rcees.ac.cn [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Huijuan [University of Chinese Academy of Sciences, Beijing 100049 (China); State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085 (China); Qu, Jiuhui [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China)

2017-05-05

Highlights: • Doping of Ce into Fe{sub 3}O{sub 4} was achieved based on a facile solvothermal method. • After doping, the removal capacity was increased by 5 times for “Sb(V)” and 2 times for “Sb(III)”. • Decreasing pH improved adsorption of Sb(V) but decreased adsorption of Sb(III). • Antimony sorption mechanisms on Ce-doped Fe{sub 3}O{sub 4} were illustrated. - Abstract: Aqueous antimony (Sb) pollution from human activity is of great concern in drinking water due to its adverse health effect. Magnetic Fe{sub 3}O{sub 4} particles, with high separation ability from solution, have been considered as a low-cost Sb adsorbent for contaminants. However, the limited adsorption capacity has restricted its practical application. In this study, a solvothermal approach was developed for doping Ce(III) into Fe{sub 3}O{sub 4}, thereby increasing the adsorption efficacy for both Sb(III) and Sb(V). In contrast to un-doped Fe{sub 3}O{sub 4}, the adsorption capacity towards Sb(III) and Sb(V) in Ce-doped materials increased from 111.4 to 224.2 mg/g and from 37.2 to 188.1 mg/g at neutral pH, respectively. Based on the combined results of XPS, XRD, and FTIR, it confirmed that Ce atom successfully doped into the Fe{sub 3}O{sub 4} structure, resulting in the decreased particle size, increased the surface area, and isoelectric point. Furthermore, the vibrating sample magnetometer (VSM) results showed that the Ce doping process had some side effects on the primitive magnetic property, but remaining the high separation potential during water treatment. According to the high removal efficiency and magnetic property, the Ce-doped Fe{sub 3}O{sub 4} of great simplicity should be a promising adsorbent for aqueous Sb removal.

Transparent nanostructured Fe-doped TiO2 thin films prepared by ultrasonic assisted spray pyrolysis technique

Science.gov (United States)

Rasoulnezhad, Hossein; Hosseinzadeh, Ghader; Ghasemian, Naser; Hosseinzadeh, Reza; Homayoun Keihan, Amir

2018-05-01

Nanostructured TiO2 and Fe-doped TiO2 thin films with high transparency were deposited on glass substrate through ultrasonic-assisted spray pyrolysis technique and were used in the visible light photocatalytic degradation of MB dye. The resulting thin films were characterized by scanning electron microscopy (SEM), Raman spectroscopy, photoluminescence spectroscopy, x-ray diffraction (XRD), and UV-visible absorption spectroscopy techniques. Based on Raman spectroscopy results, both of the TiO2 and Fe-doped TiO2 films have anatase crystal structure, however, because of the insertion of Fe in the structure of TiO2 some point defects and oxygen vacancies are formed in the Fe-doped TiO2 thin film. Presence of Fe in the structure of TiO2 decreases the band gap energy of TiO2 and also reduces the electron–hole recombination rate. Decreasing of the electron–hole recombination rate and band gap energy result in the enhancement of the visible light photocatalytic activity of the Fe-doped TiO2 thin film.

Study of cerium doped magnetite (Fe3O4:Ce)/PMMA nanocomposites

International Nuclear Information System (INIS)

Padalia, Diwakar; Johri, U.C.; Zaidi, M.G.H.

2012-01-01

The paper presents the synthesis and properties of polymer nanocomposite material based on cerium doped magnetite (Fe 3 O 4 ) as filler material and poly methyl methacrylate (PMMA) as host matrix. The magnetite (Fe 3 O 4 ) particles were synthesized by co-precipitation route using stable ferrous and ferric salts with ammonium hydroxide as precipitating agent. Further, they doped by cerium oxide (CeO 2 ) non-stoichiometrically. The composite material was fabricated by solvent evaporation method. Here 2.4 GHz microwaves were used to study the effect of microwaves heating on polymerization. The phase and crystal structure is determined by X-ray diffraction (XRD). The average crystallite size of the composites varies from 28 to 35 nm. The chemical structure is confirmed by Fourier transform infrared (FTIR) spectroscopy. The magnetic and thermal properties are investigated by vibrating sample magnetometer (VSM) and differential scanning calorimetry (DSC). The thermal study shows that the microwave heated samples possess higher glass transition temperature (T g ). The magnetic results suggest that coercivity (H C ) and squareness (M r /M s ) of the loop increases with increasing doping percent of cerium.

Shielding behavior of V2O5 doped lead borate glasses towards gamma irradiation

International Nuclear Information System (INIS)

Ghoneim, N.A.; ElBatal, H.A.; Abdelghany, A.M.; Ali, I.S.

2011-01-01

Highlights: → Base lead borate glass together with samples of the same composition doped with varying V 2 O 5 contents were prepared. → UV-visible and infrared spectroscopy were measured before and after successive gamma irradiation. → Glass samples are observed to absorb strongly in the UV. → Infrared absorption spectra indicate the presence of both triangular and tetrahedral borate groups besides the sharing of lead ions in network forming and network modifying sites. - Abstract: Undoped lead borate glass of the composition PbO 70%-B 2 O 3 30% together with samples of the same composition and doped with varying V 2 O 5 contents were prepared. UV-visible absorption spectra were measured out in the range 200-1500 nm before and after successive gamma irradiation. Infrared absorption measurements within the range 4000-400 cm -1 were carried out for the undoped and V 2 O 5 doped samples before gamma irradiation and after being irradiated with a dose of 6 Mrad. All the glass samples are observed to absorb strongly in the UV region due to the combined contributions of absorption due to trace iron impurities and that from the divalent lead Pb 2+ ions. The V 2 O 5 -doped glasses reveal extra visible absorption bands which are attributed to the existence of V 3+ ions in measurable content but not neglecting the other valence states of vanadium ions (V 4+ , V 5+ ). Infrared absorption spectra indicate the presence of both triangular and tetrahedral borate groups besides the sharing of lead ions in network forming and network modifying sites.

Low Concentration Fe-Doped Alumina Catalysts Using Sol-Gel and Impregnation Methods: The Synthesis, Characterization and Catalytic Performance during the Combustion of Trichloroethylene

Directory of Open Access Journals (Sweden)

Carolina Solis Maldonado

2014-03-01

Full Text Available The role of iron in two modes of integration into alumina catalysts was studied at 0.39 wt% Fe and tested in trichloroethylene combustion. One modified alumina was synthesized using the sol-gel method with Fe added in situ during hydrolysis; another modification was performed using calcined alumina, prepared using the sol-gel method and impregnated with Fe. Several characterization techniques were used to study the level of Fe modification in the γ-Al2O3 phase formed and to correlate the catalytic properties during trichloroethylene (TCE combustion. The introduction of Fe in situ during the sol-gel process influenced the crystallite size, and three iron species were generated, namely, magnetite, maghemite and hematite. The impregnated Fe-alumina formed hematite and maghemite, which were highly dispersed on the γ-Al2O3 surface. The X-ray photoelectron spectra (XPS, FT-IR and Mössbauer spectroscopy analyses revealed how Fe interacted with the γ-Al2O3 lattice in both catalysts. The impregnated Fe-catalyst showed the best catalytic performance compared to the catalyst that was Fe-doped in situ by the sol-gel method; both had better catalytic activity than pure alumina. This difference in activity was correlated with the accessibility of the reactants to the hematite iron species on the surface. The chlorine poisoning for all three catalysts was less than 1.8%.

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

Synthesis and characterization of hollow {alpha}-Fe{sub 2}O{sub 3} sub-micron spheres prepared by sol-gel

Energy Technology Data Exchange (ETDEWEB)

Leon, Lizbet, E-mail: lizbetlf@gmail.com; Bustamante, Angel; Osorio, Ana; Olarte, G. S. [Universidad Nacional Mayor de San Marcos (Peru); Santos Valladares, Luis De Los, E-mail: ld301@cam.ac.uk; Barnes, Crispin H. W. [University of Cambridge, Cavendish Laboratory (United Kingdom); Majima, Yutaka [Tokyo Institute of Technology, Materials and Structures Laboratory (Japan)

2011-11-15

In this work we report the preparation of magnetic hematite hollow sub-micron spheres ({alpha}-Fe{sub 2}O{sub 3}) by colloidal suspensions of ferric nitrate nine-hydrate (Fe(NO{sub 3}){sub 3}{center_dot}9H{sub 2}O) particles in citric acid solution by following the sol-gel method. After the gel formation, the samples were annealed at different temperatures in an oxidizing atmosphere. Annealing at 180 Degree-Sign C resulted in an amorphous phase, without iron oxide formation. Annealing at 250 Degree-Sign C resulted in coexisting phases of hematite, maghemite and magnetite, whereas at 400 Degree-Sign C, only hematite and maghemite were found. Pure hematite hollow sub-micron spheres with porous shells were formed after annealing at 600 Degree-Sign C. The characterization was performed by X-ray diffraction (XRD), Moessbauer spectroscopy (MS) and scanning electron microscopy (SEM).

Physical properties of Fe doped Mn3O4 thin films synthesized by SILAR method and their antibacterial performance against E. coli

Directory of Open Access Journals (Sweden)

M.R. Belkhedkar

2016-09-01

Full Text Available Nanocrystalline Fe doped Mn3O4 thin films were deposited by successive ionic layer adsorption and reaction method onto glass substrates. The X-ray diffraction study revealed that Fe doped Mn3O4 films are nanocrystalline in nature. The morphological investigations were carried out by using field emission scanning electron and atomic force microscopy studies. The optical absorption measurements showed that Mn3O4 films exhibit direct band gap energy of the order of 2.78 eV and it increased to 2.89 eV as the percentage of Fe doping in it increases from 0 to 8 wt.%. The room temperature electrical resistivity of Mn3O4 increases from 1.84 × 103 to 2.64 × 104 Ω cm as Fe doping increases from 0 to 8 wt.%. The SILAR grown Mn3O4 showed antibacterial performance against Escherichia coli bacteria which improved remarkably with doping.

Structural, magnetic and electric properties of Nd and Ni co-doped BiFeO3 materials

Directory of Open Access Journals (Sweden)

Dao Viet Thang

2017-09-01

Full Text Available Multiferroic Bi1−xNdxFe0.975Ni0.025O3 (x = 0.00, 0.05, 0.10, 0.125, and 0.15 (BNFNO and BiFeO3 (BFO materials were synthesized by a sol-gel method. Crystal structure, ferromagnetic and ferroelectric properties of the as-synthesized materials were investigated. Results showed that Nd3+ and Ni2+ co-doping affected to the electrical leakage, enhanced ferroelectric polarization and magnetization of BiFeO3. Co-doped sample with 12.5 mol% of Nd3+ and 2.5 mol% of Ni2+ exhibited an enhancement in both ferromagnetism and ferroelectric properties up to MS ~ 0.528 emu/g and PS ~ 18.35 μC/cm2 with applied electric field at 5 kV/cm, respectively. The origins of ferromagnetism and ferroelectricity enhancement were discussed in the paper.

Preparation of poly (styrene)-b-poly (acrylic acid)/{gamma}-Fe{sub 2}O{sub 3} composites

Energy Technology Data Exchange (ETDEWEB)

Zhang, L.D. [School of Materials Science and Engineering, Shandong Polytechnic University, Key Laboratory of Processing and Testing Technology of Glass Functional Ceramics of Shandong Province, Daxue Road, Western University Science Park, Jinan 250353 (China); Liu, W.L., E-mail: wlliu@sdu.edu.cn [School of Materials Science and Engineering, Shandong Polytechnic University, Key Laboratory of Processing and Testing Technology of Glass Functional Ceramics of Shandong Province, Daxue Road, Western University Science Park, Jinan 250353 (China); Xiao, C.L.; Yao, J.S.; Fan, Z.P.; Sun, X.L.; Zhang, X.; Wang, L. [School of Materials Science and Engineering, Shandong Polytechnic University, Key Laboratory of Processing and Testing Technology of Glass Functional Ceramics of Shandong Province, Daxue Road, Western University Science Park, Jinan 250353 (China); Wang, X.Q. [State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China)

2011-12-15

The use of a block copolymer, poly (styrene)-b-poly (acrylic acid) (PS-b-PAA) to prepare a magnetic nanocomposite was investigated. Poly (styrene)-poly (t-butyl acrylate) block copolymer, being synthesized by atom transfer radical polymerization, was hydrolyzed with hydrochloric acid for obtaining PS-b-PAA. The obtained PS-b-PAA was then compounded with the modified {gamma}-Fe{sub 2}O{sub 3}, and subsequently the magnetic nanocomposite was achieved. The products were characterized by {sup 1}H NMR, FTIR, gel permeation chromatography, thermogravimetric analysis, transmission electron microscopy and vibrating sample magnetometer. The results showed that the nanocomposites exhibited soft magnetism, with the mean diameter of 100 nm approximately. - Highlights: > Magnetic composites were prepared using {gamma}-Fe{sub 2}O{sub 3} and PS-b-PAA. > PS-b-PAA was synthesized by atom transfer radical polymerization. > The obtained composite exhibited soft magnetism.

Photocatalytic characteristics of single phase Fe-doped anatase TiO2 nanoparticles sensitized with vitamin B12

International Nuclear Information System (INIS)

Gharagozlou, Mehrnaz; Bayati, R.

2015-01-01

Highlights: • Anatase TiO 2 /B 12 hybrid nanostructured catalyst was successfully synthesized by sol–gel technique. • The nanoparticle catalyst was doped with iron at several concentrations. • Nanoparticles were characterized in detail by XRD, Raman, TEM, EDS, and spectroscopy techniques. • The formation mechanism and role of point defects on photocatalytic properties were discussed. • A structure-property-processing correlation was established. - Abstract: We report a processing-structure-property correlation in B 12 -anatase titania hybrid catalysts doped with several concentrations of iron. Our results clearly show that low-level iron doping alters structure, defect content, and photocatalytic characteristics of TiO 2 . XRD and Raman studies revealed formation of a single-phase anatase TiO 2 where no iron based segregation in particular iron oxide, was detected. FT-IR spectra clearly confirmed sensitization of TiO 2 nanoparticles with vitamin B 12 . TEM micrographs and diffraction patterns confirmed crystallization of anatase nanoparticles with a radius of 15–20 nm. Both XRD and Raman signals showed a peak shift and a peak broadening which are surmised to originate from creation of point defects, namely oxygen vacancy and titanium interstitial. The doped samples revealed a narrower band gap as compared to undoped samples. Photocatalytic activity of the samples was assessed through measuring the decomposition rate of rhodamine B. It was found that sensitization with vitamin B 12 and Fe-doping significantly enhances the photocatalytic efficiency of the anatase nanoparticles. We also showed that there is an optimum Fe-doping level where the maximum photocatalytic activity is achieved. The boost of photocatalytic activity was qualitatively understood to originate from a more effective use of the light photons, formation of point defects, which enhance the charge separation, higher carrier mobility

Superconductivity and magnetism in Ir-doped GdFeAsO

International Nuclear Information System (INIS)

Cui, Y.J.; Chen, Y.L.; Cheng, C.H.; Yang, Y.; Jiang, J.; Wang, Y.Z.; Zhang, Y.; Zhao, Y.

2010-01-01

The 5d-transition metal, Ir has successfully been doped at Fe site and induced superconductivity in GdFeAsO at T c = 18.9 K and ∼20 atom%. The Ir-doping shortened the c-axis length and stretched the a-axis one, which led to enhance the coupling between the FeAs- and SmO-layer, and to weaken the bonding between Fe and As atom. Paramagnetism was observed in all of the samples, which was resulted from the magnetic Gd ion as in the F-doped GdFeAsO. An upper critical field of GdFe 0.8 Ir 0.2 AsO was extrapolated to around 24 T, much smaller than that of F-doped GdFeAsO owing to a relatively low T c and small value of dH c2 /dT.

Reduced graphene oxide decorated with Fe doped SnO{sub 2} nanoparticles for humidity sensor

Energy Technology Data Exchange (ETDEWEB)

Toloman, D. [National Institute for Research and Development of Isotopic and Molecular Technologies, 67-103 Donat Street, 400293 Cluj-Napoca (Romania); Popa, A., E-mail: popa@itim-cj.ro [National Institute for Research and Development of Isotopic and Molecular Technologies, 67-103 Donat Street, 400293 Cluj-Napoca (Romania); Stan, M.; Socaci, C.; Biris, A.R. [National Institute for Research and Development of Isotopic and Molecular Technologies, 67-103 Donat Street, 400293 Cluj-Napoca (Romania); Katona, G. [Babes-Bolyai University, Faculty of Chemistry and Chemical Engineering, 11 Arany Janos Street, 400028 Cluj-Napoca (Romania); Tudorache, F. [Interdisciplinary Research Department – Field Science & RAMTECH, Al. I. Cuza University, 11 Carol I Blvd., 7000506 Iasi (Romania); Petrila, I. [Interdisciplinary Research Department – Field Science & RAMTECH, Al. I. Cuza University, 11 Carol I Blvd., 7000506 Iasi (Romania); Faculty of Automatic Control and Computer Engineering, Gheorghe Asachi Technical University, 27 Dimitrie Mangeron Street, 700050 Iasi (Romania); Iacomi, F. [Faculty of Physics, Al. I. Cuza University, 11 Carol I Blvd., 7000506 Iasi (Romania)

2017-04-30

Highlights: • Reduced graphene oxide decorated with Fe doped SnO{sub 2} nanoparticles were synthesized. • The decoration of rGO layers with SnO{sub 2}:Fe nanoparticles was highlited by TEM. • The reduction of graphene oxide was evidenced using XRD and FT-IR. • Sensitivity tests for relative humidity (RH) were carried out. • The composite sensor exhibited enhanced sensing response as compared with Fe:SnO{sub 2}. - Abstract: Reduced graphene oxide (rGO) decorated with Fe doped SnO{sub 2} nanoparticles were fabricated via the electrostatic interaction between positively charged modified Fe-doped SnO{sub 2} oxide and negatively charged graphene oxide (GO) in the presence of poly(allylamine) hydrochloride (PAH). The decoration of rGO layers with SnO{sub 2}:Fe nanoparticles was highlited by TEM microsopy. For composite sample the diffraction patterns coincide well with those of SnO{sub 2}:Fe nanoparticles. The reduction of graphene oxide was evidenced using XRD and FT-IR spectroscopy. The formation of SnO{sub 2}:Fe-PAH-graphene composites was confirmed by FT-IR, Raman and EPR spectroscopy. Sensitivity tests for relative humidity (RH) measurements were carried out at five different concentrations of humid air at room temperature. The prepared composite sensor exhibited a higher sensing response as compared with Fe:SnO{sub 2} nanoparticles.

Enhancement of magnetic and ferroelectric properties of BiFeO3 by Er and transition element (Mn, Co) co-doping

International Nuclear Information System (INIS)

Han, Yumin; Mao, Weiwei; Quan, Chuye; Wang, Xingfu; Yang, Jianping; Yang, Tao; Li, Xing’ao

2014-01-01

Highlights: • BiFeO 3 , Bi 0.8 Er 0.2 FeO 3 , Bi 0.8 Er 0.2 Fe 0.9 Mn 0.1 O 3 and Bi 0.8 Er 0.2 Fe 0.9 Co 0.1 O 3 nanoparticles were prepared by sol–gel method. • The introduction of Er and Mn, Co into BiFeO 3 leads into a phase transition with reduced grain size. • The phase transformation combined with size reduction has significantly increased saturated polarization (Ps), remanent polarization (Pr) and saturated magnetization (Ms), remanent magnetization (Mr) behaviors of the doped samples with the same variation trend. • The formation of dipolar defect complexes (DDCs) in the doped samples may also contribute to the improved ferroelectric property. • Bi 0.8 Er 0.2 Fe 0.9 Mn 0.1 O 3 exhibits significantly improved ferroelectric and ferromagnetic properties. - Abstract: BiFeO 3 (BFO), Bi 0.8 Er 0.2 FeO 3 (BEFO), Bi 0.8 Er 0.2 Fe 0.9 Mn 0.1 O 3 (BEFMO) and Bi 0.8 Er 0.2 Fe 0.9 Co 0.1 O 3 (BEFCO) nanoparticles were prepared by sol–gel method having an average size of 200 nm for BFO, under100 nm for BEFO and under 60 nm for BEFMO and BEFCO. Phase transition from a rhombohedral symmetry (R3c) for BFO to an orthorhombic symmetry (Ibmm) for BEFO, BEFMO and BEFCO has been observed. The phase transformation combined with size reduction has significantly improved both ferroelectric and ferromagnetic behaviors of the doped samples in a similar way. The formation of dipolar defect complexes (DDCs) in the doped samples also contributes to the improved ferroelectric property with saturated polarization (Ps) of 0.375 μC/cm 2 and remanent polarization (Pr) of 0.244 μC/cm 2 for BEFMO. Size effect may also impact the simultaneously developed Pr for BEFMO and BEFCO. Owning to the interactions between the ferromagnetic and antiferromagnetic microdomains, improved saturated magnetization (Ms) and remanent magnetization (Mr) are also observed in BEFMO

Removal of H₂S from Biogas by Iron (Fe³⁺ Doped MgO on Ceramic Honeycomb Catalyst using Double Packed Columns System

Directory of Open Access Journals (Sweden)

Juntima Chungsiriporn

2010-03-01

Full Text Available Hydrogen sulfide is a toxic and corrosive in nature, gas should be safely removed from the biogas streams before subjecting into the fuel cell. Fe3+ doped magnesium oxide was synthesized using sol-gel technique and dip coating process of Fe3+ doped MgO on foam ceramic honeycomb. XRD and SEM indicate that Fe3+ in Fe3+ doped MgO on foam ceramic honeycomb catalyst is finely dispersed in the MgO support. Performance of the synthesized Fe3+ doped magnesium oxide on the honeycomb catalyst was examined for hydrogen sulfide (H2S oxidation by double packed column scrubbers. The absorption column was used for H2S scrubbing from biogas by deionized water absorption and catalytic column was used as catalyst bed for degradation of absorbed H2S in scrubbing water. In the catalytic column, counter current flow of the scrubbing water and air through the catalyst pack was performed for H2S oxidation accompany with catalyst regeneration. System capacity for H2S removal from gas stream showed 98% constant along 3 hr testing time at room temperature.

Electrical and magnetic behavior of iron doped nickel titanate (Fe{sup 3+}/NiTiO{sub 3}) magnetic nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Lenin, Nayagam; Karthik, Arumugam; Sridharpanday, Mathu; Selvam, Mohanraj; Srither, Saturappan Ravisekaran; Arunmetha, Sundarmoorthy; Paramasivam, Palanisamy; Rajendran, Venkatachalam, E-mail: veerajendran@gmail.com

2016-01-01

Iron doped nickel titanate (Fe{sup 3+}/NiTiO{sub 3}) ferromagnetic nanoparticles with different concentrations of Fe (0.2, 0.4, and 0.6 mol) were synthesized using precipitation route with precursor source such as nickel nitrate and iron nitrate solutions. The prepared magnetic nanopowders were investigated through X-ray diffraction (XRD), Fourier transform infrared, scanning electron microscope, X-ray fluorescence, Brunauer–Emmett–Teller, vibrating sample magnetometer, and electrochemical impedance spectroscopy to explore the structural, ferromagnetic, and dielectric properties. The obtained XRD pattern shows formation of iron doped nickel titanate in orthorhombic structure. The crystallite size ranges from 57 to 21 nm and specific surface area ranges from 11 to 137 m{sup 2} g{sup −1}. The hysteresis loops of nanomagnetic materials show ferromagnetic behavior with higher magnitude of coercivity (H{sub c}) 867–462 Oe. The impedance analysis of ferromagnetic materials explores the ferro-dielectric behavior with enhanced properties of Fe{sup 3+}/NiTiO{sub 3} nanoparticles at higher Fe content. - Highlights: • Iron doped nickel titanate magnetic nanoparticles. • Ferromagnetic magnetism behavior with higher magnitude of coercivity. • Dielectric behavior of ferromagnetic nanoparticles with increase of Fe content.

Preparation and characterization of Fe{sub 3}O{sub 4}-Pt nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Andrade, Ângela Leão, E-mail: angelala01@hotmail.com [Federal University of Ouro Preto (UFOP), Department of Chemistry, ICEB (Brazil); Cavalcante, Luis Carlos Duarte [Federal University of Piauí (UFPI), Center of Natural Sciences (Brazil); Fabris, José Domingos [Federal University of Minas Gerais (UFMG), Department of Chemistry, ICEx (Brazil); Pereira, Márcio César [Federal University of the Jequitinhonha and Mucuri Valleys (UFVJM), Institute of Science, Engineering and Technology (Brazil); Ardisson, José Domingos [Center for the Development of the Nuclear Technology (CDTN), Laboratory of Applied Physics (Brazil); Domingues, Rosana Zacarias [Federal University of Minas Gerais (UFMG), Department of Chemistry, ICEx (Brazil)

2017-11-15

Pt and Pt-based nanomaterials are active anticancer drugs for their ability to inhibit the division of living cells. Nanoparticles of magnetite containing variable proportions of platinum were prepared in the laboratory. The magnetite nanoparticles with platinum (Pt-Fe{sub 3}O{sub 4}) were obtained by reducing the Fe{sup 3+} of the maghemite (γ Fe{sub 2}O{sub 3}) mixed with platinum (II) acetylacetonate and sucrose in two inversely coupled ceramic crucibles and heated in a furnace at 400 °C for 20 min. The formed carbon during this preparation acts to chemically reduce the ferric iron in maghemite. Moreover, its residual layer on the particle surface prevents the forming magnetite from oxidizing in air and helps retain the platinum in the solid mixture. The produced Pt-magnetite samples were characterized by {sup 57}Fe-Mössbauer spectroscopy, powder X-ray diffraction, scanning electron microscopy, and magnetization measurements. Measurements of AC magnetic-field-induced heating properties of the obtained nanocomposites, in aqueous solution, showed that they are suitable as a hyperthermia agent for biological applications.

Superconductivity and magnetism in Ir-doped GdFeAsO

Energy Technology Data Exchange (ETDEWEB)

Cui, Y.J.; Chen, Y.L. [Key Laboratory of Magnetic Levitation and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Cheng, C.H. [School of Materials Science and Engineering, University of New South Wales, Sydney 2052 NSW (Australia); Yang, Y.; Jiang, J.; Wang, Y.Z.; Zhang, Y. [Key Laboratory of Magnetic Levitation and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Zhao, Y., E-mail: yzhao@swjtu.edu.c [Key Laboratory of Magnetic Levitation and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); School of Materials Science and Engineering, University of New South Wales, Sydney 2052 NSW (Australia)

2010-11-01

The 5d-transition metal, Ir has successfully been doped at Fe site and induced superconductivity in GdFeAsO at T{sub c} = 18.9 K and {approx}20 atom%. The Ir-doping shortened the c-axis length and stretched the a-axis one, which led to enhance the coupling between the FeAs- and SmO-layer, and to weaken the bonding between Fe and As atom. Paramagnetism was observed in all of the samples, which was resulted from the magnetic Gd ion as in the F-doped GdFeAsO. An upper critical field of GdFe{sub 0.8}Ir{sub 0.2}AsO was extrapolated to around 24 T, much smaller than that of F-doped GdFeAsO owing to a relatively low T{sub c} and small value of dH{sub c2}/dT.

Pressure response of vacancy ordered maghemite (γ-Fe2O3) and high pressure transformed hematite (α-Fe2O3)

Science.gov (United States)

Hearne, Giovanni; Pischedda, Vittoria

2012-03-01

Combined XRD and Mössbauer effect spectroscopy studies to high pressures of ˜30 GPa of vacancy ordered maghemite are presented. The vacancy ordered superstructure is robust and remains intact up to the pressure-induced onset transition to hematite at 13-16 GPa. The pressure transformed hematite is shown to be crystallographically textured, unlike the randomised low pressure maghemite phase. This arises out of a pressure or stress instigated topotactic transformation of the cubic-spinel to hexagonal-corundum structure. The textured sample permits us to obtain information on the spin reorientation behavior of the pressure transformed hematite in compression and decompression sequences. Spin reorientation is restricted to ˜15° over wide pressure ranges, attributable to the effect of entrapped vacancies in the high pressure structure. Thus there are structural and magnetic peculiarities specific to pressure transformed hematite not evident in pressurized hematite starting material. These are triggered by the maghemite→hematite transformation.

Molecular adsorption of hydrogen peroxide on N- and Fe-doped titania nanoclusters

Energy Technology Data Exchange (ETDEWEB)

Mohajeri, Afshan, E-mail: amohajeri@shirazu.ac.ir; Dashti, Nasimeh Lari

2017-06-15

Highlights: • The stability and electronic properties of N/Fe-doped (TiO{sub 2}){sub n} clusters with n = 5,6 were studied. • The adsorption H{sub 2}O{sub 2} on the surface of doped clusters has been investigated. • This is the first report of H{sub 2}O{sub 2} adsorption onto the (TiO{sub 2}){sub n} cluster in the presence of metal and non-metal dopants. • The effect of N and Fe dopants on interaction strength was studied. - Abstract: Titanium dioxide (titania) nanoparticles have been extensively investigated for photocatalytic applications such as the decomposition and adsorption of pollutant and undesirable compound in air and waste water. In this context, the present article reports the molecular adsorption of hydrogen peroxide on the surface of doped titania clusters. Density functional theory calculations were performed to investigate the structures and electronic properties of two nanoscale (TiO{sub 2}){sub n} clusters (n = 5,6) modified by nitrogen and iron dopants. The relative stability of all possible N-doped and Fe-doped isomers has been compared with each other and with the parent cluster. It was found that the Fe-doped clusters are in general more stable than the N-doped counterparts. Moreover, after N/Fe doping an enhanced in the magnetization of the clusters is observed. In the second part, we have investigated different modes of H{sub 2}O{sub 2} adsorption on the lowest-energy isomers of doped clusters. In almost all the cases, the adsorptions on the doped clusters are found to be less exothermic than on the corresponding undoped parent cluster. Our results highlight the essential role of charge transfer into the interaction between H{sub 2}O{sub 2} and doped (TiO{sub 2}){sub n} clusters, especially for Fe-doped clusters.

Structural and optical properties of α-Fe2O3 nanoparticles, influence by holmium ions

Science.gov (United States)

Mathevula, L. E.; Noto, L. L.; Mothudi, B. M.; Dhlamini, M. S.

2018-04-01

α-Fe2O3 and α-Fe2O3 doped with different concentration of holmium ions were synthesized by a simple sol-gel method. The XRD data confirmed the hexagonal structure of α-Fe2O3 for un-doped and holmium doped samples. The crystallite size was found to be decreasing with increasing holmium concentration. The amount of holmium was quantified using an EDS, which shows an increase in holmium quantity as concentration increases. The UV-Vis measurement shows an absorption edge around 570 nm. The band gap was estimated using the Kubelka-Munk relation and it was found to be fluctuating between 1.94 eV and 2.04 eV. The PL spectra confirmed the effect of holmium ions on luminescence properties of α-Fe2O3 which showed a maximum intensity at 0.1 mol% Holmium, and quenching as the concentration is increased from 0.3 mol% to 0.9 mol%.

Evolution of the structural and multiferroic properties of PbFe{sub 2/3}W{sub 1/3}O{sub 3} ceramics upon Mn-doping

Energy Technology Data Exchange (ETDEWEB)

Ivanov, S.A. [Center of Materials Science, Karpov' Institute of Physical Chemistry, Vorontsovo Pole 10, Moscow, 105064 (Russian Federation); Department of Engineering Sciences, Uppsala University, Box 534, 751 21, Uppsala (Sweden); Bush, A.A. [Moscow State University of Information Technologies, RadioEngineering and Electronics, pr.Vernadskogo 78, Moscow, 119454 (Russian Federation); Ritter, C. [Institute Laue-Langevin, BP 156, F-38042, Grenoble (France); Behtin, M.A. [Moscow State University of Information Technologies, RadioEngineering and Electronics, pr.Vernadskogo 78, Moscow, 119454 (Russian Federation); Cherepanov, V.M. [National Research Centre Kurchatov Institute, pl. Kurchatova 1, Moscow, 123182 (Russian Federation); Autieri, C.; Kvashnin, Y.O.; Di Marco, I.; Sanyal, B.; Eriksson, O. [Department of Physics and Astronomy, Uppsala University, Box 516, 751 20, Uppsala (Sweden); Kumar, P. Anil; Nordblad, P. [Department of Engineering Sciences, Uppsala University, Box 534, 751 21, Uppsala (Sweden); Mathieu, R., E-mail: roland.mathieu@angstrom.uu.se [Department of Engineering Sciences, Uppsala University, Box 534, 751 21, Uppsala (Sweden)

2017-02-01

The perovskite system Pb(Fe{sub 1-x}Mn{sub x}){sub 2/3}W{sub 1/3}O{sub 3} (0 ≤ x ≤ 1, PFMWO) has been prepared by conventional solid-state reaction under different sintering conditions. Structures and phase composition as well as thermal, magnetic and dielectric properties of the compounds have been systematically investigated experimentally and by first-principles density functional calculations. A clean perovskite phase is established at room temperature for compositions 0 ≤ x ≤ 0.4. Rietveld refinements of X-ray and neutron powder diffraction patterns demonstrate that the compounds crystallize in space group Pm-3m (0 ≤ x ≤ 0.4). The degree of ordering of the Fe and W/Mn cations was found to depend on the concentration of Mn. First-principles calculations suggest that the structural properties of PFMWO are strongly influenced by the Jahn-Teller effect. The PFMWO compounds behave as relaxor ferroelectrics at weak Mn-doping with a dielectric constant that rapidly decreases with increasing Mn content. A low temperature antiferromagnetic G-type order with propagation vector k = (1/2,1/2,1/2) is derived from neutron powder diffraction data for the samples with x ≤ 0.4. However with increasing doping concentration, the magnetic order is perturbed. First-principles calculations show that the dominant exchange coupling is antiferromagnetic and occurs between nearest neighbor Fe atoms. When the system is doped with Mn, a relatively weak ferromagnetic (FM) interaction between Fe and Mn atoms emerges. However, due to the presence of this FM interaction, the correlation length of the magnetic order is greatly shortened already at rather low doping levels. - Highlights: • The perovskite system Pb(Fe{sub 1−x}Mn{sub x}){sub 2/3}W{sub 1/3}O{sub 3} (0 ≤ x ≤ 1, PFMWO) has been synthesized. • The structural, magnetic, and dielectric properties of PFMWO have been investigated. • The degree of ordering of the Fe and W/Mn cations was found to depend on x. �

Effect of Al and Fe doping in ZnO on magnetic and magneto-transport properties

International Nuclear Information System (INIS)

Kumar, Santosh; Deepika; Tripathi, Malvika; Vaibhav, Pratyush; Kumar, Aman; Kumar, Ritesh; Choudhary, R.J.; Phase, D.M.

2016-01-01

The structural, magnetic and magneto-transport of undoped ZnO, Zn_0_._9_7Al_0_._0_3O, Zn_0_._9_5Fe_0_._0_5O and Zn_0_._9_2Al_0_._0_3Fe_0_._0_5O thin films grown on Si(100) substrate using pulsed laser deposition were investigated. The single phase nature of the films is confirmed by X-ray diffraction and Raman spectroscopy measurements. The possibility of Fe metal cluster in Fe doped/co-doped films is ruled out by Fe 2p core level photoelectron spectra. From O 1s core level spectra it is observed that oxygen vacancy is present in all the films. The undoped ZnO film shows magnetic ordering below ∼175 K, whereas Fe doped/codoped samples show magnetic ordering even at 300 K. The Al doped sample reveals paramagnetic behavior. The magneto-transport measurements suggest that the mobile carriers undergo exchange interaction with local magnetic moments. - Highlights: • Al, Fe, Al–Fe co-doped and undoped films of ZnO are deposited on Si by PLD. • Single phase (002) oriented Wurtzite ZnO phase is formed for all films. • Fe doped and Fe–Al co-doped ZnO films reveal magnetic hysteresis at 300 K. • Negative magnetoresistance is observed in undoped and Fe–Al co-doped ZnO film. • It is apparent that charge carriers are coupled with the local magnetic moment.

In situ XANES studies of TiO{sub 2}/Fe{sub 3}O{sub 4}-C during photocatalytic degradation of trichloroethylene

Energy Technology Data Exchange (ETDEWEB)

Hsu, T.-F.; Hsiung, T.-L. [Department of Environmental Engineering, National Cheng Kung University, Tainan 70101, Taiwan (China); Wang, James [Department of Biomedical Engineering, University of Southern California, Los Angeles 90007 (United States); Huang, C.-H. [Department of Environmental Engineering, National Cheng Kung University, Tainan 70101, Taiwan (China); Paul Wang, H., E-mail: wanghp@mail.ncku.edu.t [Department of Environmental Engineering, National Cheng Kung University, Tainan 70101, Taiwan (China); Sustainable Environmental Research Center, National Cheng Kung University, Tainan 70101, Taiwan (China)

2010-07-21

Mainly anatase and Fe{sub 3}O{sub 4} in the magnetic photocatalysts (TiO{sub 2} on Fe{sub 3}O{sub 4}-C core-shell nanoparticles (TiO{sub 2}/Fe{sub 3}O{sub 4}-C)) are observed by X-ray powder diffraction (XRD) spectroscopy. The Ti K-edge least-square fitted XANES spectra of the TiO{sub 2}/Fe{sub 3}O{sub 4}-C photocatalyst indicate that the main titanium species are nanosize TiO{sub 2} (9 nm) (77%) and bulky TiO{sub 2} (23%). Speciation of titanium in the TiO{sub 2}/Fe{sub 3}O{sub 4}-C during photocatalytic degradation of 100 ppm of trichloroethylene (TCE) has also been studied by in situ X-ray absorption near-edge structural (XANES) spectroscopy. TiO{sub 2} is not perturbed during the course of photocatalysis. However, it is worth to note that during photocatalytic degradation of TCE, about 33% of FeO and 67% of Fe{sub 3}O{sub 4} are observed in the photocatalyst. It seems that the carbon layer on the TiO{sub 2}/Fe{sub 3}O{sub 4}-C photocatalysts can reduce the possibility for photoexcited electron-hole recombination as usually found on the relatively narrow bandgap of ferric oxide during photocatalysis.

The synergetic effect of V and Fe-co-doping in TiO{sub 2} studied from the DFT + U first-principle calculation

Energy Technology Data Exchange (ETDEWEB)

Liu, Baoshun, E-mail: liubaoshun@126.com; Zhao, Xiujian

2017-03-31

Highlights: • The effect of Fe and V doping on TiO{sub 2} structure was studied with DFT + U calculation. • V and Fe co-doping affects the formation energies and electronic structure. • V and Fe co-doping causes the synergetic effect on the optical properties. - Abstract: Based on the density functional theory (DFT + U), a detailed study on the energetic, electronic, and optical properties of Fe-, V-, and Fe & V-co-doping anatase and rutile TiO{sub 2} was performed The synergetic effect of Fe & V bimetal co-doping on the optical absorption was discussed on electronic level. Two kinds of co-dopants were considered, which included edge-shared and corner-shared co-doping. It was shown that Fe and V atoms prefer to replace Ti atom in the O-rich contions than in the Ti-rich conditions. Co-doping in anatase reduces the formation energies in both cases, while the formation energies for rutile cannot be decreased. The Bader charge analysis indicates the +3 of Fe atom and +4 of V atom, and the obvious electron exchange between Fe and V atom in co-doping cases can be identified, which indicates the presence of synergetic effect induced by co-doping. The cooperation of Fe & V co-dopants was also supported by the result of projected density of states and spin charge density differences, as the hybridization of Fe3d with V3d orbitals was seen within the TiO{sub 2} forbidden band. Different from single-dopant systems, the V3d-Fe3d co-interaction leads to the formation of some spin mid-gap states, which have an obvious effect on the optical absorptions.

Characterization of transparent superconductivity Fe-doped CuCrO{sub 2} delafossite oxide

Energy Technology Data Exchange (ETDEWEB)

Taddee, Chutirat [Materials Science and Nanotechnology Program, Faculty of Science, Khon Kaen University, Khon Kaen 40002 (Thailand); Kamwanna, Teerasak, E-mail: teekam@kku.ac.th [Department of Physics, Faculty of Science, Khon Kaen University, Khon Kaen 40002 (Thailand); Nanotec-KKU Center of Excellence on Advanced Nanomaterials for Energy Production and Storage, Khon Kaen 40002 (Thailand); Integrated Nanotechnology Research Center (INRC), Khon Kaen University, Khon Kaen 40002 (Thailand); Amornkitbamrung, Vittaya [Department of Physics, Faculty of Science, Khon Kaen University, Khon Kaen 40002 (Thailand); Nanotec-KKU Center of Excellence on Advanced Nanomaterials for Energy Production and Storage, Khon Kaen 40002 (Thailand); Integrated Nanotechnology Research Center (INRC), Khon Kaen University, Khon Kaen 40002 (Thailand)

2016-09-01

Graphical abstract: - Highlights: • Effect of Fe substitution on the physical properties in CuCrO{sub 2} is studied. • The substitution of Cr{sup 3+} by Fe{sup 3+} produces a mixed effect on the magnetic properties. • CuCr{sub 1−x}Fe{sub x}O{sub 2} delafossite oxides show transparent superconductivity. - Abstract: Delafossite CuCr{sub 1−x}Fe{sub x}O{sub 2} (0.0 ≤ x ≤ 0.15) semiconductors were synthesized using a self-combustion urea nitrate process. The effects of Fe concentration on its microstructural, optical, magnetic, and electrical properties were investigated. X-ray diffraction (XRD) analysis results revealed the delafossite structure in all the samples. The lattice spacing of CuCr{sub 1−x}Fe{sub x}O{sub 2} slightly increased with increasing substitution of Fe at the Cr sites. The optical properties measured at room temperature using UV–visible spectroscopy showed a weak absorbability in the visible light and near IR regions. The corresponding direct optical band gap was about 3.61 eV, exhibiting transparency in the visible region. The magnetic hysteresis loop measurements showed that the Fe-doped CuCrO{sub 2} samples exhibited ferromagnetic behavior at room temperature. This indicated that the substitution of Fe{sup 3+} for Cr{sup 3+} produced a mixed effect on the magnetic properties of CuCrO{sub 2} delafossite oxide. The temperature dependent resistivity measurements clearly revealed the presence of superconductivity in the CuCr{sub 1−x}Fe{sub x}O{sub 2} with a superconducting transition up to 118 K.

Iron doped SnO{sub 2}/Co{sub 3}O{sub 4} nanocomposites synthesized by sol-gel and precipitation method for metronidazole antibiotic degradation

Energy Technology Data Exchange (ETDEWEB)

Agarwal, Shilpi [Department of Applied Chemistry, University of Johannesburg, Johannesburg (South Africa); Tyagi, Inderjeet [Department of Chemistry, Indian Institute of Technology Roorkee, 247667 (India); Gupta, Vinod Kumar, E-mail: vinodg@uj.ac.za [Department of Applied Chemistry, University of Johannesburg, Johannesburg (South Africa); Sohrabi, Maryam; Mohammadi, Sanaz [Department of Chemistry, Shahr-e-Qods Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Golikand, Ahmad Nozad, E-mail: anozad@aeoi.org.ir [Department of Chemistry, Shahr-e-Qods Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Jaber Research Laboratory, NSTRI, P.O. Box: 14395-836, Tehran (Iran, Islamic Republic of); Fakhri, Ali, E-mail: ali.fakhri88@yahoo.com [Young Researchers and Elites Club, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of)

2017-01-01

Sol-gel and precipitation reaction methods were used to synthesize Un-doped and Fe-doped SnO{sub 2}/Co{sub 3}O{sub 4} nanocomposites under UV light; the synthesized nanocomposites were applied for the photocatalytic degradation of metronidazole antibiotic. The developed photo catalyst was well characterized using energy dispersive X-ray spectrometer (EDX), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), field emission scanning electron microscopy (FE-SEM), UV–Visible and photoluminescence (PL) spectroscopy. Effective parameters such as pH, photocatalyst dose and contact time was optimized and well investigated. From the obtained facts it is clear that the 98.3% of MTZ was degraded with in 15 min, pH 6 and 0.1 g catalyst when the Fe molar ratio was 1:1 at %. As compared to results obtained from un-doped SnO{sub 2}/Co{sub 3}O{sub 4} nanocomposites Fe doped SnO{sub 2}/Co{sub 3}O{sub 4} nanocomposites possess greater photocatalytic efficiency. - Graphical abstract: Surface textural and morphological presentation. - Highlights: • Un-doped and Fe-doped SnO{sub 2}/Co{sub 3}O{sub 4} nanocomposites were applied as photocatalyst. • The nanocomposites exhibited photocatalytic property under UV light. • The maximum degradation was observed for Fe-doped SnO{sub 2}/Co{sub 3}O{sub 4} (1:1) photocatalyst. • 0.1 g photocatalyst is sufficient to carry out 98.3% degradation of MTZ.

First principles study of magneto-optical properties of Fe-doped ZnO

Energy Technology Data Exchange (ETDEWEB)

Shaoqiang, Guo [College of Science, Inner Mongolia University of Technology, Hohhot 010051 (China); Qingyu, Hou, E-mail: by0501119@126.com [College of Science, Inner Mongolia University of Technology, Hohhot 010051 (China); Zhenchao, Xu [College of Science, Inner Mongolia University of Technology, Hohhot 010051 (China); Chunwang, Zhao [College of Science, Inner Mongolia University of Technology, Hohhot 010051 (China); College of Arts and Sciences, Shanghai Maritime University, Shanghai 201306 (China)

2016-12-15

Studies on optical band gaps and absorption spectra of Fe-doped ZnO have conflicting conclusions, such as contradictory redshifted and blueshifted spectra. To solve this contradiction, we constructed models of un-doped and Fe-doped ZnO using first-principles theory and optimized the geometry of the three models. Electronic structures and absorption spectra were also calculated using the GGA+U method. Higher doping content of Fe resulted in larger volume of doped system, and higher total energy resulted in lower stability. Higher formation energy also led to more difficult doping. Meanwhile, the band gaps broadened and the absorption spectra exhibited an evident blue shift. The calculations were in good agreement with the experimental results. Given the unipolar structure of ZnO, four possible magnetic coupling configurations for Zn{sub 14}Fe{sub 2}O{sub 16} were calculated to investigate the magnetic properties. Results suggest that Fe doping can improve ferromagnetism in the ZnO system and that ferromagnetic stabilization was mediated by p–d exchange interaction between Fe-3d and O-2p orbitals. Therefore, the doped system is expected to obtain high stability and high Curie temperature of diluted magnetic semiconductor material, which are useful as theoretical bases for the design and preparation of the Fe-doped ZnO system’s magneto-optical properties. - Highlights: • A biomonitoring tool for the freshwater zone of template estuaries. • Water quality characterization related to nutrients and organic matter enrichment. • The percentage of a group of 24 tolerant species were capable of detecting the impairment of the water quality. • Characterization of morpho-functional traits of the selected tolerant species.

Functional doped metal oxide films. Zinc oxide (ZnO) as transparent conducting oxide (TCO) titanium dioxide (TiO{sub 2}) as thermographic phosphor and protective coating

Energy Technology Data Exchange (ETDEWEB)

Nebatti Ech-Chergui, Abdelkader

2011-07-29

Metalorganic chemical vapor deposition (MOCVD) was used in the present work. Un-doped and Al-doped ZnO films were developed using two reactors: Halogen Lamp Reactor (HLR) (a type of Cold Wall Reactor) and Hot Wall Reactor (HWR), and a comparison was made between them in terms of the film properties. Zinc acetylacetonate was used as precursor for ZnO films while aluminum acetylacetonate was used for doping. The amount of Al doping can be controlled by varying the gas flow rate. Well ordered films with aluminum content between 0 and 8 % were grown on borosilicate glass and silicon. The films obtained are 0.3 to 0.5 {mu}m thick, highly transparent and reproducible. The growth rate of ZnO films deposited using HLR is less than HWR. In HLR, the ZnO films are well oriented along c-axis ((002) plane). ZnO films are commonly oriented along the c-axis due to its low surface free energy. On the other hand, the HWR films are polycrystalline and with Al doping these films aligned along the a-axis ((100) plane) which is less commonly observed. The best films were obtained with the HLR method showing a minimum electrical resistivity of 2.4 m{omega}cm and transmittance of about 80 % in the visible range. The results obtained for Al-doped films using HLR are promising to be used as TCOs. The second material investigated in this work was un-doped and doped titanium dioxide (TiO{sub 2}) films- its preparation and characterization. It is well known that thermographic phosphors can be used as an optical method for the surface temperature measurement. For this application, the temperature-dependent luminescence properties of europium (III)-doped TiO{sub 2} thin films were studied. It was observed that only europium doped anatase films show the phosphorescence. Rutile phase do not show phosphorescence. The films were prepared by the sol-gel method using the dip coating technique. The structures of the films were determined by X-ray diffraction (XRD). The excitation and the emission

3d-metal doping (Fe,Co,Ni,Zn) of the high T/sub c/ perovskite YBa/sub 2/Cu/sub 3/O/sub 7-y/

International Nuclear Information System (INIS)

Tarascon, J.M.; Barboux, P.; Greene, L.H.; Hull, G.W.; Bagley, B.G.

1988-01-01

The structural, magnetic and superconducting properties of the mixed compounds YBa/sub 2/Cu/sub 3-x/M/sub x/O/sub 7-y/ (M = Ni, Zn, Fe and Co) are reported. Values of y, determined by titration, are found to be dependent on the nature and amount of the doping. The range of solubility is greater for the Fe and Co compounds (chi = 1) than for those with Ni or Zn (chi = 0.3). The undoped material is orthorhombic and remains orthorhombic after substitution for Cu by Ni or Zn, whereas a tetragonal phase is observed when Fe, Co are substituted for Cu. DC resistance and AC susceptibility measurements show that T/sub c/ is depressed from 90K (chi = 0) to 45K (chi = 0.2) for both the Ni and Zn doped compounds and T/sub c/ is destroyed in the Fe and Co doped compounds when chi reaches 0.4. The authors suggest that a valance of 2 be assigned to the Ni and Zn and 3 to the Fe and Co ions

Microscopic studies of a SnO2/α-Fe2O3 architectural nanocomposite using Moessbauer spectroscopic and magnetic measurements

International Nuclear Information System (INIS)

Hayashi, Naoaki; Muranaka, Shigetoshi; Yamamoto, Shinpei; Takano, Mikio; Zhang Dongfeng; Sun Lingdong; Yan Chunhua

2008-01-01

A SnO 2 /α-Fe 2 O 3 architectural nanocomposite, which was evidenced as SnO 2 nanorod arrays assembled on the surface of α-Fe 2 O 3 nanotubes in our previous study, was investigated microscopically by means of Moessbauer spectroscopic and magnetic measurements. It was found for the SnO 2 nanorods that Fe 3+ ions substituted slightly to Sn 0.998 Fe 0.002 O 2 . Concerning the α-Fe 2 O 3 tubes, the Morin transition, which was completely suppressed in the mother, SnO 2 -free α-Fe 2 O 3 nanotubes, was found to be recovered locally. We speculate that it takes place in the interface area as a result of structural modification needed for the connection with the SnO 2 nanorods. - Graphic abstract: 57 Fe Moessbauer spectrum of SnO 2 /α-Fe 2 O 3 architectural nanocomposite evidenced as SnO 2 nanorod arrays assembled on the surface of α-Fe 2 O 3 nanotubes. (I: Fe-doped SnO 2 nanorods, II: α-Fe 2 O 3 nanotubes) It was found for the SnO 2 nanorods that Fe 3+ ions substituted slightly to Sn 0.998 Fe 0.002 O 2

Magnetic and luminescent properties of Fe/Fe{sub 3}O{sub 4}-Y{sub 2}O{sub 3}:Eu nanocomposites

Energy Technology Data Exchange (ETDEWEB)

Wang Qin [College of Chemistry, Jilin University, Changchun 130012 (China); College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot (China); Yang Xuwei; Yu Lianxiang [College of Chemistry, Jilin University, Changchun 130012 (China); Yang Hua, E-mail: huayang86@sina.com [College of Chemistry, Jilin University, Changchun 130012 (China)

2011-09-15

Highlights: > We synthesize multifunctional Fe/Fe{sub 3}O{sub 4}-Y{sub 2}O{sub 3}:Eu nanocomposites. > The luminescent and magnetic properties of the nanocomposites are researched. > The nanocomposites showed both ferrimagnetic behavior and unique europium fluorescence properties with high emission intensity. > The spectra changes induced by the UV light irradiation and the magnetic field have been systematically studied and compared in detail. > And the hysteresis curve changes induced by the UV light irradiation have been discussed. - Abstract: Multifunctional nanocomposites with Fe/Fe{sub 3}O{sub 4} nanoparticles as the core and europium-doped yttrium oxide (Y{sub 2}O{sub 3}:Eu) as the shell (Fe/Fe{sub 3}O{sub 4}-Y{sub 2}O{sub 3}:Eu) have been obtained successfully employing a solvothermal method. The nanocomposites showed both ferrimagnetic behavior and unique europium fluorescence properties with high emission intensity. The spectra changes induced by the UV light irradiation and the magnetic field have been systematically studied and compared in detail. The relationship between fluorescence and magnetic properties of the multifunctional nanocomposites has been investigated in our manuscript. These multifunctional nanocomposites could be used in a number of biomedical applications, such as drug targeting, cell separation and bioimaging.

Enhanced magnetic and dielectric behavior in Co doped BiFeO{sub 3} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Chakrabarti, Kaushik; Sarkar, Babusona; Ashok, Vishal Dev [Department of Materials Science, Indian Association for the Cultivation of Science, Jadavpur, Kolkata-700032 (India); Chaudhuri, Sheli Sinha [Department of Electronics and Telecommunication Engineering, Jadavpur University, Kolkata-700032 (India); De, S.K., E-mail: msskd@iacs.res.in [Department of Materials Science, Indian Association for the Cultivation of Science, Jadavpur, Kolkata-700032 (India)

2015-05-01

Magnetic and dielectric properties of Co doped BiFeO{sub 3} (BFO) nanoparticles (13 nm) have been investigated. The dopant Co{sup 2+} converts spherical morphology to cubic nanostructures. The significant changes in temperature dependence of magnetization may be due to magnetic disorder phase induced by divalent Co. The substitution of Fe by Co disrupts cycloidal spin structure of BFO and improves the ferromagnetic property. Enhancement of the saturation magnetization and coercivity by about 10 times in doped BFO are due to changes in morphology. High dielectric constant of about 670 and low loss at room temperature show Co doped BFO as promising material for multifunctional devices.

Magnetic and electron spin resonance studies of W doped CoFe2O4 polycrystalline materials

Science.gov (United States)

Singamaneni, S. R.; Martinez, L. M.; Swadipta, R.; Ramana, C. V.

2018-05-01

We report the magnetic and electron spin resonance (ESR) properties of W doped CoFe2O4 polycrystalline materials, prepared by standard solid-state reaction method. W was doped (0-15%) in CFO lattice on Fe site. Isothermal magnetization measurements reveal that the coercive field (Hc) (1300-2200 Oe) and saturation magnetization MS (35-82 emu/g) vary strongly as a function of W doping at all the temperatures (4-300 K) measured. We believe that a strong decrease in magnetic anisotropy in CFO after doping with W could cause a decrease in Hc. Up on doping CFO with W in place of Fe, the process transforms part of Fe3+ into Fe2+ due to the creation of more oxygen vacancies. This hinders the super-exchange interaction between Fe3+ and Fe2+, which causes a decrease in MS. Zero-field cooled (ZFC) and field cooled (FC, 1000 Oe) magnetization responses measured at 4 K on 1% W doped CFO show no indication of exchange bias, inferring that there are no other microscopic secondary magnetic phases (no segregation). This observation is corroborated by ESR (9.398 GHz) measurements collected as a function of temperature (10-150 K) and W doping (0-15%). We find that ESR spectra did not change after doping with W above 0.5%. However, ESR spectra collected from 0.5% W doped CFO sample showed a strong temperature dependence. We observed several ESR signals from 0.5% W doped CFO sample that could be due to phase separation.

Magnetic and electron spin resonance studies of W doped CoFe2O4 polycrystalline materials

Directory of Open Access Journals (Sweden)

S. R. Singamaneni

2018-05-01

Full Text Available We report the magnetic and electron spin resonance (ESR properties of W doped CoFe2O4 polycrystalline materials, prepared by standard solid-state reaction method. W was doped (0-15% in CFO lattice on Fe site. Isothermal magnetization measurements reveal that the coercive field (Hc (1300-2200 Oe and saturation magnetization MS (35-82 emu/g vary strongly as a function of W doping at all the temperatures (4-300 K measured. We believe that a strong decrease in magnetic anisotropy in CFO after doping with W could cause a decrease in Hc. Up on doping CFO with W in place of Fe, the process transforms part of Fe3+ into Fe2+ due to the creation of more oxygen vacancies. This hinders the super-exchange interaction between Fe3+ and Fe2+, which causes a decrease in MS. Zero-field cooled (ZFC and field cooled (FC, 1000 Oe magnetization responses measured at 4 K on 1% W doped CFO show no indication of exchange bias, inferring that there are no other microscopic secondary magnetic phases (no segregation. This observation is corroborated by ESR (9.398 GHz measurements collected as a function of temperature (10-150 K and W doping (0-15%. We find that ESR spectra did not change after doping with W above 0.5%. However, ESR spectra collected from 0.5% W doped CFO sample showed a strong temperature dependence. We observed several ESR signals from 0.5% W doped CFO sample that could be due to phase separation.

Preparation of nanocomposites resin from seed Pterodon emarginatus doped maghemite nanoparticles.

Science.gov (United States)

Silveira, L B; Martins, Q S; Maia, J C; Santos, J G

2012-06-01

Electrical characterization and magnetic nanocomposite resin seeds Pterodon emarginatus (PE) doped with nanoparticles of maghemite and treated by different chemical processes is reported in this paper. The pure PE resin showed semiconducting characteristics probably the presence of natural iron oxide in its molecular structure. The analysis of Mössbauer spectra pure resin showed two magnetic sites presented on measurements made at temperature of 300 K. Six "LEDs" to have been doped maghemite nanoparticles forming concentrations of 2.6 x 10(15) to 1.56 x 10(16) particles/cm2 forming the LED-PEMN. In the presence of the applied current versus voltage (0 to 0.9 V) LED-PEMN shown semiconducting properties. In the presence of frequency versus voltage sample of pure resin and LED features small decrease. While samples of LED-PEMN suffers loss frequency linearly with concentration and voltage. The pure PE resin shows high resistance to the applied voltage while the LED-PEMN is observed linear increase with the strength and concentration of nanoparticles of maghemite.

In situ observation of transformation in alpha-Fe sub 2 O sub 3 under hydrogen implantation

CERN Document Server

Watanabe, Y; Ishikawa, N; Furuya, K; Kato, M

2002-01-01

An in situ observation of the alpha-Fe sub 2 O sub 3 -to-Fe sub 3 O sub 4 transformation has been performed using a dual-ion-beam accelerator interfaced with a transmission electron microscope (TEM). During the hydrogen-ion implantation of alpha-Fe sub 2 O sub 3 , transformation into the new phase (gamma-Fe sub 2 O sub 3 or Fe sub 3 O sub 4) was observed. It was also found that the orientation relationship between alpha-Fe sub 2 O sub 3 and the new phase (gamma-Fe sub 2 O sub 3 or Fe sub 3 O sub 4) satisfies the Shoji-Nishiyama relationship, in agreement with previous experiments. It was also found that the nearest interatomic distance does not vary by the implantation until the re-stacked phase appears, although when the re-stacked phase is formed, the lattice expansion is observed in the transformed (re-stacked) phase. Judging from these results, we have concluded that the alpha-Fe sub 2 O sub 3 to Fe sub 3 O sub 4 transformation is induced during the hydrogen ion implantation of alpha-Fe sub 2 O sub 3.

Structural phase transition and magnetic properties of Er-doped BiFeO3 nanoparticles

International Nuclear Information System (INIS)

Li, Y T; Zhang, H G; Dong, X G; Li, Q; Mao, W W; Dong, C L; Ren, S L; Li, X A; Wei, S Q

2013-01-01

The structural phase transition and local structural distortion of Er-doped BiFeO 3 nanoparticles have been discussed in order to understand the variation of magnetic properties in this system. The X-ray diffraction patterns and X-ray absorption fine structure of these samples demonstrate that there is structural phase transition and no obvious local structural distortion with the increasing of doping concentration. Unfortunately, no ferromagnetic properties have been observed even at a lower temperature. And the X-ray absorption spectra of Fe 2p core level of these samples are totally same, especially the energy positions do not shift which means the consistent valence states of Fe ions.

Properties of half metallic (Ba0.8Sr0.2)2-x La2x/3x/3FeMoO6 double perovskites

International Nuclear Information System (INIS)

Serrate, D.; De Teresa, J.M.; Blasco, J.; Morellon, L.; Ibarra, M.R.

2005-01-01

Previous work in (Ba 0.8 Sr 0.2 ) 2- x La x FeMoO 6 and Ba 1+ x Sr 1-3 x La 2 x FeMoO 6 have stated electron doping as the most important parameter in terms of T c enhancement. Here we report complementary structural, magnetic and transport properties, say a series where there is no doping and only structural parameters are changed: (Ba 0.8 Sr 0.2 ) 2- x La 2 x /3 x /3 FeMoO 6 . We propose a complete phase diagram where structural and bandfilling impact on the Curie temperature is clearly evidenced

Investigation of the physical, optical, and photocatalytic properties of CeO2/Fe-doped InVO4 composite

Science.gov (United States)

Chaison, Jindaporn; Wetchakun, Khatcharin; Wetchakun, Natda

2017-12-01

The CeO2/Fe-doped InVO4 composites with various Fe concentrations (0.5, 1.0, 2.0, 5.0 and 6.0 mol%) was synthesized by homogeneous precipitation and hydrothermal methods. The as-synthesized samples were characterized by powder X-ray diffraction (XRD), Brunauer Emmett and Teller (BET)-specific surface area, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and UV-visible diffuse reflectance spectroscopy (DRS). Fe-doping into InVO4 crystal induces the distortion of the crystalline structure, the transformation of InVO4 morphology, and the new energy subband level generation of Fe between the CB and VB edge of InVO4. The electron excitation from the VB to Fe orbitals results in the decreased band gap and the extended absorption of visible-light, and thus enhances its photocatalytic performance. Visible-light-driven photocatalytic degradation of Rhodamine B (RhB) dye in water was used to evaluate the photocatalytic performance of CeO2/Fe-doped InVO4 composites. The results revealed that there is an optimum Fe (5.0 mol %) doping level. The composite with the optimum doping level obtains high photocatalytic activity of CeO2/Fe-doped InVO4 composite compared to pure CeO2 and pure InVO4 host. The increase of photocatalytic activity of CeO2/Fe-doped InVO4 composite was ascribed to the surface area, crystal defect, and band gap energy. Moreover, the photocatalytic enhancement is also because iron ions act as a trapping site, which results in the higher separation efficiency of photogenerated electrons and holes pairs in the CeO2/InVO4 composite. The evaluation of radical scavengers confirmed that hydroxyl radical was the main active species during the photodegradation of RhB. These synergistic effects are responsible for the enhanced photocatalytic activity of CeO2/Fe-doped InVO4 composite. Furthermore, the possible enhanced photocatalytic mechanism

Effects of (La, Sr) co-doping on electrical conduction and magnetic properties of BiFeO3 nanoparticles

International Nuclear Information System (INIS)

Liu Li; Wang Shouyu; Yin Zi; Zhang Chuang; Li Xiu; Yang Jiabin; Liu Weifang; Xu Xunling

2016-01-01

Multiferroic material as a photovoltaic material has gained considerable attention in recent years. Nanoparticles (NPs) La 0.1 Bi 0.9−x Sr x FeO y (LBSF, x = 0, 0.2, 0.4) with dopant Sr 2+ ions were synthesized by the sol–gel method. A systematic change in the crystal structure from rhombohedral to tetragonal upon increasing Sr doping was observed. There is an obvious change in the particle size from 180 nm to 50 nm with increasing Sr substitution into LBFO. It was found that Sr doping effectively narrows the band gap from ∼ 2.08 eV to ∼ 1.94 eV, while it leads to an apparent enhancement in the electrical conductivity of LBSF NPs, making a transition from insulator to semiconductor. This suggests an effective way to modulate the conductivity of BiFeO 3 -based multiferroic materials with pure phase by co-doping with La and Sr at the A sites of BiFeO 3 . (paper)

Photocatalytic behaviors and structural characterization of nanocrystalline Fe-doped TiO2 synthesized by mechanical alloying

International Nuclear Information System (INIS)

Kim, Dong Hyun; Hong, Hyun Seon; Kim, Sun Jae; Song, Jae Sung; Lee, Kyung Sub

2004-01-01

Nanocrystalline Fe-doped TiO 2 powders were synthesized by mechanical alloying (MA) with varying Fe contents from 0 up to 4.8 wt.% to shift the absorption threshold into the visible light region. The photocatalytic feasibility of the Fe-doped TiO 2 powder was evaluated by quantifying the visible light absorption capacity using ultraviolet and visible (UV-Vis) spectroscopy and photoluminescence spectroscopy. Effects of Fe additions on the crystal structures and the morphologies of the Fe-doped powders were also investigated as a function of the doping content using transmission electron microscopy-electron diffraction pattern (TEM-EDP), X-ray diffraction (XRD) and energy dispersive X-ray (EDAX) and X-ray photoelectron spectroscopy (XPS). The UV-Vis study showed that the UV absorption for the Fe-doped powder moved to a longer wavelength (red shift) and the photoefficiency was enhanced. Based on the analysis of the photoluminescence spectra, the red shift was believed to be induced by localizing the dopant level near the valence band of TiO 2 . The UV-Vis absorption depended on the Fe concentration. TEM-EDP and XRD investigations showed that the Fe-doped powder had a rutile phase in which the added Fe atoms were dissolved. The rutile phase was composed of spherical particles and chestnut bur shaped particles, resulting in a larger surface area than the spherical P-25 powder

Ni-doped α-Fe 2 O 3 as electron transporting material for planar heterojunction perovskite solar cells with improved efficiency, reduced hysteresis and ultraviolet stability

Energy Technology Data Exchange (ETDEWEB)

Guo, Ying; Liu, Tao; Wang, Ning; Luo, Qiang; Lin, Hong; Li, Jianbao; Jiang, Qinglong; Wu, Lili; Guo, Zhanhu

2017-08-01

We report on high-efficiency planar heterojunction perovskite solar cells (PSCs) employing Ni-doped alpha-Fe2O3 as electron-transporting layer (ETL). The suitable addition of nickel (Ni) dopant could enhance the electron conductivity as well as induce downward shift of the conduction band minimum for alpha-Fe2O3, which facilitate electrons injection and transfer from the conduction band of the perovskite. As a consequence, a substantial reduction in the charge accumulation at the perovskite/ETL interface makes the device much less sensitive to scanning rate and direction, i.e., lower hysteresis. With a reverse scan for the optimized PSC under standard AM-1.5 sunlight illumination, it generates a competitive power conversion efficiency (PCE) of 14.2% with a large short circuit current (J(sc)) of 22.35 mA/cm(2), an open circuit photovoltage (V-oc) of 0.92 V and a fill factor (FF) of 69.1%. Due to the small J-V hysteresis behavior, a higher stabilized PCE up to 11.6% near the maximum power point can be reached for the device fabricated with 4 mol% Ni-doped alpha-Fe2O3 ETL compared with the undoped alpha-Fe2O3 based cell (9.2%). Furthermore, a good stability of devices with exposure to ambient air and high levels of ultraviolet (UV)-light can be achieved. Overall, our results demonstrate that the simple solution-processed Ni-doped alpha-Fe2O3 can be a good candidate of the n-type collection layer for commercialization of PSCs.

Room temperature ferromagnetism in Fe-doped CuO nanoparticles.

Science.gov (United States)

Layek, Samar; Verma, H C

2013-03-01

The pure and Fe-doped CuO nanoparticles of the series Cu(1-x)Fe(x)O (x = 0.00, 0.02, 0.04, 0.06 and 0.08) were successfully prepared by a simple low temperature sol-gel method using metal nitrates and citric acid. Rietveld refinement of the X-ray diffraction data showed that all the samples were single phase crystallized in monoclinic structure of space group C2/c with average crystallite size of about 25 nm and unit cell volume decreases with increasing iron doping concentration. TEM micrograph showed nearly spherical shaped agglomerated particles of 4% Fe-doped CuO with average diameter 26 nm. Pure CuO showed weak ferromagnetic behavior at room temperature with coercive field of 67 Oe. The ferromagnetic properties were greatly enhanced with Fe-doping in the CuO matrix. All the doped samples showed ferromagnetism at room temperature with a noticeable coercive field. Saturation magnetization increases with increasing Fe-doping, becomes highest for 4% doping then decreases for further doping which confirms that the ferromagnetism in these nanoparticles are intrinsic and are not resulting from any impurity phases. The ZFC and FC branches of the temperature dependent magnetization (measured in the range of 10-350 K by SQUID magnetometer) look like typical ferromagnetic nanoparticles and indicates that the ferromagnetic Curie temperature is above 350 K.

Study of cerium doped magnetite (Fe{sub 3}O{sub 4}:Ce)/PMMA nanocomposites

Energy Technology Data Exchange (ETDEWEB)

Padalia, Diwakar, E-mail: Padalia.diwakar@gmail.com [Department of Physics, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India); Johri, U.C. [Department of Physics, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India); Zaidi, M.G.H. [Supercritical Fluid Processing Laboratory, Department of Chemistry, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India)

2012-03-01

The paper presents the synthesis and properties of polymer nanocomposite material based on cerium doped magnetite (Fe{sub 3}O{sub 4}) as filler material and poly methyl methacrylate (PMMA) as host matrix. The magnetite (Fe{sub 3}O{sub 4}) particles were synthesized by co-precipitation route using stable ferrous and ferric salts with ammonium hydroxide as precipitating agent. Further, they doped by cerium oxide (CeO{sub 2}) non-stoichiometrically. The composite material was fabricated by solvent evaporation method. Here 2.4 GHz microwaves were used to study the effect of microwaves heating on polymerization. The phase and crystal structure is determined by X-ray diffraction (XRD). The average crystallite size of the composites varies from 28 to 35 nm. The chemical structure is confirmed by Fourier transform infrared (FTIR) spectroscopy. The magnetic and thermal properties are investigated by vibrating sample magnetometer (VSM) and differential scanning calorimetry (DSC). The thermal study shows that the microwave heated samples possess higher glass transition temperature (T{sub g}). The magnetic results suggest that coercivity (H{sub C}) and squareness (M{sub r}/M{sub s}) of the loop increases with increasing doping percent of cerium.

Investigation on compression behavior of TZM and La{sub 2}O{sub 3} doped TZM Alloys at high temperature

Energy Technology Data Exchange (ETDEWEB)

Hu, Ping, E-mail: huping1985@126.com [School of Metallurgy Engineering, Xi’an University of Architecture and Technology, Xi’an 710055 (China); Zhou, Yuhang; Chang, Tian; Yu, Zhitao; Wang, Kuaishe; Yang, Fan; Hu, Boliang [School of Metallurgy Engineering, Xi’an University of Architecture and Technology, Xi’an 710055 (China); Cao, Weicheng [Jinduicheng Molybdenum Co., Ltd, Xi’an 710077 (China); Yu, Hailiang [School of Mechanical, Materials, Mechatronic Engineering, University of Wollongong, Wollongong, NSW 2500 (Australia)

2017-02-27

Mechanical properties of Titanium-zirconium-molybdenum (TZM) and La{sub 2}O{sub 3} doped TZM alloys under compression were tested at 1000 °C and 1200 °C. Microstructure of TZM and La{sub 2}O{sub 3} doped TZM alloys after compressing was characterized by scanning electron microscopy. The effects on La{sub 2}O{sub 3} doping on the high temperature deformation behavior and microstructure evolution of the TZM alloy were analyzed. Results show that La{sub 2}O{sub 3} doping can refine the grain size of TZM alloy. La{sub 2}O{sub 3} doping changes fracture model of TZM alloy. TZM alloy exhibits mainly intergranular fracture, while the La{sub 2}O{sub 3} doped TZM alloy exhibits both intergranular and transgranular fracture mode.

Comparative assessment of the efficiency of Fe-doped TiO2 prepared by two doping methods and photocatalytic degradation of phenol in domestic water suspensions

Directory of Open Access Journals (Sweden)

Mst. Shamsun Nahar, Kiyoshi Hasegawa, Shigehiro Kagaya and Shigeyasu Kuroda

2007-01-01

Full Text Available Fe-doped TiO2 particles responding to visible light were synthesized by impregnation and calcination method using TiO2 particle and Ti element, respectively. The optical and the chemical properties were characterized by measuring the X-ray diffraction (XRD and UV–visible spectroscopy. The onset of absorption shifted to longer wavelengths on doping TiO2 by the calcination process, which showed a better response as compared to the impregnation method. The photocatalytic reactivity was evaluated by the degradation of phenol with impregnated Fe-doped (0.5% w/w in Fe and calcined Fe-doped (FexTi1−xO2, x=0.005 (Fe/Ti molar ratio TiO2 separately in distilled and tap water. The characterization results have confirmed the advanced possibility of correlation between photoactivity and the special property of sulfur-containing calcined Fe-doped TiO2. In case of the coagulation of the undoped A-I and the Fe-doped B-I, the photoactivity showed a decrease due to the presence of natural electrolytes and due to the high pH of tap water, whereas in the case of the coagulation of calcined Fe-doped TiO2 prepared from sulfides (FexTiS2, the photoactivity showed an increase. In this study, highest catalytic activity was found to be strongly dependent both on catalyst structure and on the type of water used.

Electronic conduction in doped multiferroic BiFeO3

Science.gov (United States)

Yang, Chan-Ho; Seidel, Jan; Kim, Sang-Yong; Gajek, M.; Yu, P.; Holcomb, M. B.; Martin, L. W.; Ramesh, R.; Chu, Y. H.

2009-03-01

Competition between multiple ground states, that are energetically similar, plays a key role in many interesting material properties and physical phenomena as for example in high-Tc superconductors (electron kinetic energy vs. electron-electron repulsion), colossal magnetoresistance (metallic state vs. charge ordered insulating state), and magnetically frustrated systems (spin-spin interactions). We are exploring the idea of similar competing phenomena in doped multiferroics by control of band-filling. In this paper we present systematic investigations of divalent Ca doping of ferroelectric BiFeO3 in terms of structural and electronic conduction properties as well as diffusion properties of oxygen vacancies.

Photocatalytic characteristics of single phase Fe-doped anatase TiO{sub 2} nanoparticles sensitized with vitamin B{sub 12}

Energy Technology Data Exchange (ETDEWEB)

Gharagozlou, Mehrnaz, E-mail: gharagozlou@icrc.ac.ir [Department of Nanomaterials and Nanotechnology, Institute for Color Science and Technology, Tehran (Iran, Islamic Republic of); Bayati, R. [Intel Corporation, IMO-SC, SC2, Santa Clara, CA 95054 (United States)

2015-01-15

Highlights: • Anatase TiO{sub 2}/B{sub 12} hybrid nanostructured catalyst was successfully synthesized by sol–gel technique. • The nanoparticle catalyst was doped with iron at several concentrations. • Nanoparticles were characterized in detail by XRD, Raman, TEM, EDS, and spectroscopy techniques. • The formation mechanism and role of point defects on photocatalytic properties were discussed. • A structure-property-processing correlation was established. - Abstract: We report a processing-structure-property correlation in B{sub 12}-anatase titania hybrid catalysts doped with several concentrations of iron. Our results clearly show that low-level iron doping alters structure, defect content, and photocatalytic characteristics of TiO{sub 2}. XRD and Raman studies revealed formation of a single-phase anatase TiO{sub 2} where no iron based segregation in particular iron oxide, was detected. FT-IR spectra clearly confirmed sensitization of TiO{sub 2} nanoparticles with vitamin B{sub 12}. TEM micrographs and diffraction patterns confirmed crystallization of anatase nanoparticles with a radius of 15–20 nm. Both XRD and Raman signals showed a peak shift and a peak broadening which are surmised to originate from creation of point defects, namely oxygen vacancy and titanium interstitial. The doped samples revealed a narrower band gap as compared to undoped samples. Photocatalytic activity of the samples was assessed through measuring the decomposition rate of rhodamine B. It was found that sensitization with vitamin B{sub 12} and Fe-doping significantly enhances the photocatalytic efficiency of the anatase nanoparticles. We also showed that there is an optimum Fe-doping level where the maximum photocatalytic activity is achieved. The boost of photocatalytic activity was qualitatively understood to originate from a more effective use of the light photons, formation of point defects, which enhance the charge separation, higher carrier mobility.

Towards hybrid biocompatible magnetic rHuman serum albumin-based nanoparticles: use of ultra-small (CeLn)3/4+ cation-doped maghemite nanoparticles as functional shell

Science.gov (United States)

Israel, Liron L.; Kovalenko, Elena I.; Boyko, Anna A.; Sapozhnikov, Alexander M.; Rosenberger, Ina; Kreuter, Jörg; Passoni, Lorena; Lellouche, Jean-Paul

2015-01-01

Human serum albumin (HSA) is a protein found in human blood. Over the last decade, HSA has been evaluated as a promising drug carrier. However, not being magnetic, HSA cannot be used for biomedical applications such as magnetic resonance imaging (MRI) and magnetic drug targeting. Therefore, subsequent composites building on iron oxide nanoparticles that are already used clinically as MRI contrast agents are extensively studied. Recently and in this context, innovative fully hydrophilic ultra-small CAN-stabilized maghemite ((CeLn)3/4+-γ-Fe2O3) nanoparticles have been readily fabricated. The present study discusses the design, fabrication, and characterization of a dual phase hybrid core (rHSA)-shell ((CeLn)3/4+-γ-Fe2O3 NPs) nanosystem. Quite importantly and in contrast to widely used encapsulation strategies, rHSA NP surface-attached (CeLn)3/4+-γ-Fe2O3 NPs enabled to exploit both rHSA (protein functionalities) and (CeLn)3/4+-γ-Fe2O3 NP surface functionalities (COOH and ligand L coordinative exchange) in addition to very effective MRI contrast capability due to optimal accessibility of H2O molecules with the outer magnetic phase. Resulting hybrid nanoparticles might be used as a platform modular system for therapeutic (drug delivery system) and MR diagnostic purposes.

Preparation of raspberry-like γ-Fe2O3/crackled nitrogen-doped carbon capsules and their application as supports to improve catalytic activity.

Science.gov (United States)

Zhang, Junshuai; Yao, Tongjie; Zhang, Hui; Zhang, Xiao; Wu, Jie

2016-11-10

In this manuscript, we have introduced a novel method to improve the catalytic activity of metal nanoparticles via optimizing the support structure. To this end, raspberry-like γ-Fe 2 O 3 /crackled nitrogen-doped carbon (CNC) capsules were prepared by a two-step method. Compared with traditional magnetic capsules, in γ-Fe 2 O 3 /CNC capsules, the γ-Fe 2 O 3 nanoparticles were embedded in a CNC shell; therefore, they neither occupied the anchoring sites for metal nanoparticles nor came into contact with them, which was beneficial for increasing the metal nanoparticle loading. Numerous tiny cracks appeared on the porous CNC shell, which effectively improved the mass diffusion and transport in catalytic reactions. Additionally, the coordination interaction could be generated between the precursor metal ions and doped-nitrogen atoms in the capsule shell. With the help of these structural merits, γ-Fe 2 O 3 /CNC capsules were ideal supports for Pd nanoparticles, because they were beneficial for improving the Pd loading, reducing the nanoparticle size, increasing their dispersity and maximizing the catalytic performance of Pd nanoparticles anchored on the inner shell surface. As expected, γ-Fe 2 O 3 /CNC@Pd catalysts exhibited a dramatically enhanced catalytic activity towards hydrophilic 4-nitrophenol and hydrophobic nitrobenzene. The reaction rate constant k was compared with recent work and the corresponding reference samples. Moreover, they could be easily recycled by using a magnet and reused without an obvious loss of catalytic activity.

Recyclable UV and visible light photocatalytically active amorphous TiO2 doped with M (III) ions (M = Cr and Fe)

International Nuclear Information System (INIS)

Buddee, Supat; Wongnawa, Sumpun; Sirimahachai, Uraiwan; Puetpaibool, Walailak

2011-01-01

Research highlights: → The low photocatalytic activity of amorphous TiO2 was enhanced by doping with Cr(III) or Fe(III) ions. → The doped catalysts performed close to P25 under UV light and better with visible light. → The doped catalysts can be recycled. - Abstract: Samples of amorphous TiO 2 doped with Cr(III) and Fe(III), designated as Cr-TiO 2 and Fe-TiO 2 , were prepared via modified impregnation method. The resulting products were characterized by X-ray diffraction, scanning electron microscopy, specific surface area by the Brunauer, Emmett and Teller method, UV-vis absorption and diffuse reflectance spectroscopy, and electron spin resonance spectroscopy. Experimental results revealed that the concentrations of dopants under studied, from 0.05 to 0.2 mol%, had no effect on the phase of products. The band gap energies shifted from 3.28 eV in the undoped amorphous TiO 2 to 2.50 eV and 2.86 eV for Fe-TiO 2 and Cr-TiO 2 , respectively. The doped amorphous TiO 2 showed photocatalytic activities under both UV and visible light with optimal results at 0.1 mol% dopants. Under UV irradiation, the 0.1 mol% doped samples decolorized methylene blue solutions to the same extent as the commercial TiO 2 samples (P25 and anatase) in 5 h. Under visible light, the doped samples decolorized dye solutions in 12 h while the commercial ones were much less active. The used catalysts can be recycled many times without any special treatment.

Structural and optical characterization of p-type highly Fe-doped SnO2 thin films and tunneling transport on SnO2:Fe/p-Si heterojunction

Science.gov (United States)

Ben Haj Othmen, Walid; Ben Hamed, Zied; Sieber, Brigitte; Addad, Ahmed; Elhouichet, Habib; Boukherroub, Rabah

2018-03-01

Nanocrystalline highly Fe-doped SnO2 thin films were prepared using a new simple sol-gel method with iron amounts of 5, 10, 15 and 20%. The obtained gel offers a long durability and high quality allowing to reach a sub-5 nm nanocrystalline size with a good crystallinity. The films were structurally characterized through X-ray diffraction (XRD) that confirms the formation of rutile SnO2. High Resolution Transmission Electron Microscopy (HRTEM) images reveals the good crystallinity of the nanoparticles. Raman spectroscopy shows that the SnO2 rutile structure is maintained even for high iron concentration. The variation of the PL intensity with Fe concentration reveals that iron influences the distribution of oxygen vacancies in tin oxide. The optical transmittance results indicate a redshift of the SnO2 band gap when iron concentration increases. The above optical results lead us to assume the presence of a compensation phenomenon between oxygen vacancies and introduced holes following Fe doping. From current-voltage measurements, an inversion of the conduction type from n to p is strongly predicted to follow the iron addition. Electrical characterizations of SnO2:Fe/p-Si and SnO2:Fe/n-Si heterojunctions seem to be in accordance with this deduction. The quantum tunneling mechanism is expected to be important at high Fe doping level, which was confirmed by current-voltage measurements at different temperatures. Both optical and electrical properties of the elaborated films present a particularity for the same iron concentration and adopt similar tendencies with Fe amount, which strongly correlate the experimental observations. In order to evaluate the applicability of the elaborated films, we proceed to the fabrication of the SnO2:Fe/SnO2 homojunction for which we note a good rectifying behavior.

Impact effects of gamma irradiation on the optical and FT infrared absorption spectra of some Nd3+-doped soda lime phosphate glasses

Science.gov (United States)

Marzouk, M. A.; Elkashef, I. M.; Elbatal, H. A.

2018-04-01

The main aim of the present work is to study by two collective optical and FTIR spectral measurements some prepared Nd2O3-doped soda lime phosphate glasses before and after gamma irradiation with dose (9 Mrad). The spectral data reveal two strong UV absorption peaks which are correlated with unavoidable trace iron impurities beside extended additional characteristic bands due to Nd3+ ions. Gamma irradiation on the undoped glass produces slight decrease of the intensity of the UV absorption and the generation of an induced visible band and these effects are controlled with two photochemical reduction of some Fe3+ ions to Fe2+ ions together with the formation of nonbridging oxygen hole center (NBOHC) or phosphorous oxygen hole center (POHC). The impact effect of gamma irradiation on the spectra of Nd2O3-doped glasses is limited due to suggested shielding behavior of neodymium ions. FT-infrared spectra show vibrational modes due to main Q2-Q3 phosphate groups and the response of gamma irradiation of the IR spectra is low and the limited variations are related to suggested changes in some bond angles and bond lengths which cause the observed decrease to the intensities of some IR bands.

Doping effects of Fe ion on magnetic anisotropy of YBa2Cu3Oy

International Nuclear Information System (INIS)

Ugawa, T.; Horii, S.; Maeda, T.; Haruta, M.; Shimoyama, J.

2013-01-01

Highlights: •We clarified orientation effects of Fe-doped Y123 in modulated rotating fields. •Y123 showed two different hard magnetic axes due to twin microstructures. •The two hard magnetic axes in Fe-doped Y123 were [1 0 0] and [1 1 0] directions. •Magnetic anisotropy of the [1 1 0] grain was higher than that of the [1 0 0] grain. -- Abstract: We report magnetic alignment of YBa 2 (Cu 1−x Fe x ) 3 O y (Fe-doped Y123, x = 0–0.1) powders under modulated rotation magnetic fields (MRFs) and roles of Fe ion as a determination factor of magnetic anisotropy in Y123. The Fe-free and Fe-doped Y123 powder samples aligned in the MRF of 10 T showed two different orientation types of the hard axis in Y123 grains. From an X-ray rocking curve measurement for the magnetically aligned powder samples of the Fe-doped Y123, inplane magnetic anisotropy for Y123 grains with the hard axis parallel to the [1 1 0] direction was found to be higher than that for Y123 grains with the hard axis parallel to the [0 1 0] direction

Magnetic and ferroelectric properties of Fe doped SrTiO{sub 3-{delta}} films

Energy Technology Data Exchange (ETDEWEB)

Kumar, A Sendil; Suresh, P; Srinath, S [School of Physics, University of Hyderabad, Hyderabad, 500 046 (India); Kumar, M Mahesh; Post, M L [Institute for Chemical Process and Environmental Technology, National Research Council of Canada, Ottawa, ON, K1A 0R6 (Canada); Srikanth, H [Materials Physics Laboratory, Department of Physics, University of South Florida, Tampa, Florida, 33620 (United States); Sahner, Kathy; Moos, Ralf, E-mail: sssp@uohyd.ernet.i [Functional Materials, University of Bayreuth, 95447, Bayreuth (Germany)

2010-01-01

Recent interest in SrTiO{sub 3} stems from its wide applicability in microwave devices based on the tunable characteristics of dielectric constant in the microwave frequency range. It is obvious that for any such application, SrTiO{sub 3} should have a ferroelectric Curie temperature (T{sub C}) close to room temperature or higher. By inducing strains by chemical substitutions, it was possible to obtain T{sub C} as high as 200{sup 0}C in SrTiO{sub 3} modified with Fe{sup 4+}. Hysteresis loops obtained confirms the presence of ferroelectric domains. Two apparent transitions, one at {approx}200 {sup 0}C and another {approx}300 {sup 0}C were seen in {epsilon}', which are replicated as sharp drops in resistivity curves. These temperatures far exceed the T{sub C}s reported in the literature till now and could open new avenues for innumerable other applications for SrTiO{sub 3}. The magnetic properties of Fe doped SrTiO{sub 3} are also investigated. Low doping of Fe exhibits simple antiferromagnetic behaviour.

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.

The phase diagram and magnetic properties of Co and Ti co-doped (1−x)BiFeO_3–xLaFeO_3 solid solutions

International Nuclear Information System (INIS)

Wu, Jiangtao; Xu, Jun; Li, Nan; Jiang, Yaqi; Xie, Zhaoxiong

2015-01-01

Single phase Co and Ti co-doped Bi_1_−_xFeO_3−La_xFeO_3 (x = 0–1) solid solutions were prepared by the sol–gel method. Room temperature x-ray powder diffraction (XRD) patterns showed that the structures of as-prepared Bi_1_−_xLa_xFe_0_._9_0Co_0_._0_5Ti_0_._0_5O_3 solid solutions transformed from rhombohedral R3c to tetragonal P4mm and then to orthorhombic Pnma, with increasing La concentration from 0 to 1. In situ high-temperature XRD (HTXRD) analysis further revealed that rhombohedral structure R3c (x ≤ 0.16) and tetragonal structure P4mm (0.17 ≤ x ≤ 0.40) changed to orthorhombic Pnma along with increasing temperature, and the phase transition temperature decreased with the increase of La doping concentration. However, the orthorhombic structure Pnma (x ≥ 0.41) kept stable even when the temperature reached 850 °C. The phase diagram of as-prepared binary solid solutions of Bi_1_−_xLa_xFe_0_._9_0Co_0_._0_5Ti_0_._0_5O_3(x = 0–1) was drawn on the basis of XRD and HTXRD analysis. Magnetic measurement revealed that the magnetic properties are greatly enhanced with the increase of La content. - Highlights: • Single phase Co and Ti co-doped (1−x)BiFeO_3–xLaFeO_3 (x = 0–1) solid solutions were synthesized. • The phase transitions were investigated by tuning composition and temperature. • Phase diagram was constructed according to the results of XRD for the first time. • The magnetization of solid solution can be enhanced when increasing La content.

Visible light photocatalysts (Fe, N):TiO{sub 2} from ammonothermally processed, solvothermal self-assembly derived Fe-TiO{sub 2} mesoporous microspheres

Energy Technology Data Exchange (ETDEWEB)

Zou, Mingming; Xiong, Fengqiang; Ganeshraja, Ayyakannu Sundaram [Dalian Institute of Chemical Physics (DICP), Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, Liaoning, 116023 (China); Feng, Xiaohua; Wang, Chuanxi [Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201 (China); Thomas, Tiju, E-mail: tijuthomas@iitm.ac.in [Department of Metallurgical and Materials Engineering, Indian Institute of Technology Madras, Chennai, 600036, Tamil Nadu (India); Yang, Minghui, E-mail: myang@dicp.ac.cn [Dalian Institute of Chemical Physics (DICP), Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, Liaoning, 116023 (China)

2017-07-01

Iron (III) and nitrogen co-doped mesoporous TiO{sub 2} microspheres (Fe-N-TiO{sub 2}) are prepared using a self-assembly based solvothermal process followed by an ammonothermal method. Among all samples, 1 mol.% of Fe dopants and 500 °C nitridation (for 2 h) gives the highest visible light photoactivity. Results imply that the Fe{sup 3+}/Fe{sup 2+} dopant trap energy level introduced within the band gap in mildly Fe (∼1 at%) doped TiO{sub 2} and the mesoporous nature of the material, both aid in the observed catalytic performance. Subjecting Fe-TiO{sub 2} samples to ammonothermal process induces oxygen vancancies, and substitutional and interstitial N. This reduces optical band gap, and introduces local states. The lower band gap and local states together aid in the absorption of visible light and separation of charge carriers. Co-dopants are distributed uniformly in the best photocatalysts. The active species generated in the photocatalytic system is shown to be singlet molecular oxygen ({sup 1}O{sub 2}) using selective radical quenchers. - Highlights: • Iron (III) and nitrogen co-doped mesoporous TiO{sub 2} microspheres (Fe-N-TiO{sub 2}) are prepared. • Fe{sup 3+}/Fe{sup 2+} dopant trap energy level introduced within the band gap in Fe (∼1 at%) doped TiO{sub 2}. • Subjecting Fe-TiO{sub 2} samples to ammonothermal process induces oxygen vancancies, and causes substitutional and interstitial N. • Co-dopants are distributed uniformly in the best photocatalysts. • Active species generated is shown to be singlet molecular oxygen ({sup 1}O{sub 2}).

Thermoluminescence of LaAlO3 crystals doped with Eu and Ce - Dy ions exposed to ultraviolet and gamma radiation

International Nuclear Information System (INIS)

Oliveira, Vitor H.; Faria, Luiz O.; Silva, Edna S.

2011-01-01

Due to environmental problems such as degradation of the ozone layer and control of radiation levels in units of radiation, new dosimetric materials with high sensitivity for ultraviolet (UV) and gamma radiation are of great interest for applications in environmental dosimetry. In this context, this paper presents the results of a systematic investigation of the thermoluminescent (TL) response of LaAlO 3 crystals doped with different concentrations of trivalent optically active ions exposed to UV and gamma radiation doses. The work has been performed under a direct cooperation between the Institute of Inorganic Chemistry in Moscow (IGIC), responsible for crystal growth, and the Center for Development of Nuclear Technology (CDTN), responsible for the study of its luminescent properties. In this context, samples doped with 1% of Eu 3+ , 1% Ce 3+ , 5% of Ce 3+ and also co-doped with 5% Ce 3+ and 1% Dy 3+ were grown under hydrothermal conditions. The investigation was divided into two fronts, one for gamma radiation and the other for UV radiation. In the investigation with gamma radiation the best TL response has been obtained from LaAlO 3 :Eu. This crystal has shown good sensitivity and excellent linearity between TL output and the delivered gamma doses ranging from 0.1 to 10.0 mGy. In addition, its TL curve is quite similar to the Al 2 O 3 :C, a commercial TL phosphor with high sensitivity to gamma radiation. In the investigation with UV radiation the best response has been achieved for co-doped LaAlO 3 :Ce,Dy. They have excellent sensitivity and good linearity for spectral irradiances ranging from 0.042 to 1.2 mJ.cm -2 . (author)

Fe(Ⅲ) ions enhanced catalytic properties of (BiO)2CO3 nanowires and mechanism study for complete degradation of xanthate.

Science.gov (United States)

Guo, Yujiao; Cui, Kuixin; Hu, Mingyi; Jin, Shengming

2017-08-01

The wire-like Fe 3+ -doped (BiO) 2 CO 3 photocatalyst was synthesized by a hydrothermal method. The photocatalytic property of Fe 3+ -doped (BiO) 2 CO 3 nanowires was evaluated through degradation of sodium isopropyl xanthate under UV-visible light irradiation. The as-prepared Fe 3+ -doped (BiO) 2 CO 3 nanowires were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), UV-visible diffuse reflectance spectroscopy (UV-vis DRS), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) in detail. The results of XRD showed that the crystallinity of (BiO) 2 CO 3 nanowires decreased when Fe 3+ ions were introduced into the solution system. XPS results illustrated that xanthate could be absorbed on the surface of Fe 3+ -doped (BiO) 2 CO 3 nanowires to produce BiS bond at the beginning of the reaction, which could broaden the visible light absorption. FTIR spectra confirmed the formation of SO 4 2- after photocatalytic decomposition of xanthate solution. The Fe 3+ -doped (BiO) 2 CO 3 nanowires showed an enhanced photocatalytic activity for decomposition of xanthate due to the narrower band gap and larger BET surface area, comparing with pure (BiO) 2 CO 3 nanowires. By the results of UV-vis spectra of the solution and FTIR spectra of recycled Fe 3+ -doped (BiO) 2 CO 3 , the xanthate was oxidized completely into CO 2 and SO 4 2- . The photocatalytic degradation process of xanthate followed a pseudo-second-order kinetics model. The mechanism of enhanced photocatalytic activity was proposed as well. Copyright © 2017 Elsevier Ltd. All rights reserved.

A simple way to prepare reduced graphene oxide nanosheets/Fe2O3-Pd/N-doped carbon nanosheets and their application in catalysis.

Science.gov (United States)

Yao, Tongjie; Zhang, Junshuai; Zuo, Quan; Wang, Hao; Wu, Jie; Zhang, Xiao; Cui, Tieyu

2016-04-15

The catalysts with Pd and γ-Fe2O3 nanoparticles embedded between reduced graphene oxide nanosheets (rGS) and N-doped carbon nanosheets (NCS) were prepared through a two-step method. Firstly, graphene oxide nanosheets (GS)/prussian blue (PB)-Pd/polypyrrole (PPy) composites were synthesized by using pyrrole monomer as reductant, K3Fe(CN)6 and PdCl2 as oxidants in the presence of GS via a redox reaction. Subsequently, the as-obtained GS/PB-Pd/PPy composites were calcinated in N2 atmosphere. During the heat-treatment, carbonization of PPy to NCS, conversion of nonmagnetic PB to magnetic γ-Fe2O3 nanoparticles, and reduction of GS to rGS were finished, simultaneously. rGS/Fe2O3-Pd/NCS composites exhibited good catalytic activity toward reduction of 4-nitrophenol. The rate constant k and turnover frequency were calculated and compared with recent reports. Owing to γ-Fe2O3 nanoparticles, the rGS/Fe2O3-Pd/NCS composites could be quickly separated by magnet and reused without obvious decrease in activity. Copyright © 2016 Elsevier Inc. All rights reserved.

Electron and hole doping effects in Sr{sub 2}FeMoO{sub 6} double perovskites

Energy Technology Data Exchange (ETDEWEB)

Sanchez, D. E-mail: diana.sanchez@icmm.csic.es; Alonso, J.A.; Garcia-Hernandez, M.; Martinez-Lope, M.J.; Casais, M.T.; Martinez, J.L.; Fernandez-Diaz, M.T

2004-05-01

Electron and hole doping effects in the ferromagnetic and structural properties of the double perovskite Sr{sub 2}FeMoO{sub 6} are studied along the series Sr{sub 2-x}La{sub x}FeMoO{sub 6} (0{<=}x{<=}1) and Sr{sub 2-x}FeMoO{sub 6} (0{<=}x{<=}0.4) from neutron powder diffraction and magnetization data. Sr-deficient samples (hole doped) show moderate changes in the structure and both T{sub c} and M{sub s} rapidly decrease with x. On the contrary, a change from tetragonal to monoclinic symmetry and a non monotonic behaviour in T{sub c} is found in the La-substituted series (electron doped)

Evaluation of surface energy state distribution and bulk defect concentration in DSSC photoanodes based on Sn, Fe, and Cu doped TiO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Ako, Rajour Tanyi [Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, BE1410, Negara (Brunei Darussalam); Ekanayake, Piyaisiri, E-mail: piyasiri.ekanayake@ubd.edu.bn [Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, BE1410, Negara (Brunei Darussalam); Young, David James [Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, BE1410, Negara (Brunei Darussalam); Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology and Research -A*STAR, 3 Research Link, 117602 (Singapore); Faculty of Science, Health, Education and Engineering, University of the Sunshine Coast, Locked Bag 4, Maroochydore DC, Queensland, 4558 (Australia); Hobley, Jonathan [Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, BE1410, Negara (Brunei Darussalam); Chellappan, Vijila [Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology and Research - A*STAR, 3 Research Link, 117602 (Singapore); Tan, Ai Ling [Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, BE1410, Negara (Brunei Darussalam); Gorelik, Sergey; Subramanian, Gomathy Sandhya [Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology and Research - A*STAR, 3 Research Link, 117602 (Singapore); Lim, Chee Ming [Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, BE1410, Negara (Brunei Darussalam)

2015-10-01

Graphical abstract: - Highlights: • The structural, optical and optoelectronic properties of 1 mol.% Fe, Sn and Cu doped TiO{sub 2} have been compared. • Transient lifetimes for pure TiO{sub 2} and Sn doped TiO{sub 2} were considerably shorter than Fe and Cu doped TiO{sub 2}. • A good correlation between the bulk defects and transient decay for the doped TiO{sub 2} powders was observed. • Photon to current conversion efficiency of DSSC based on the metal doped TiO{sub 2} were in order Sn-TiO{sub 2} > Cu-TiO{sub 2} > Pure >> Fe-TiO{sub 2}. • DSSC based on Fe doped photoanodes is limited by a high concentration of surface free holes observed at 433 nm. - Abstract: Electron transfer dynamics in the oxide layers of the working electrodes in both dye-sensitized solar cells and photocatalysts greatly influences their performance. A proper understanding of the distribution of surface and bulk energy states on/in these oxide layers can provide insights into the associated electron transfer processes. Metal ions like Iron (Fe), Copper (Cu) and Tin (Sn) doped onto TiO{sub 2} have shown enhanced photoactivity in these processes. In this work, the structural, optical and transient properties of Fe, Cu and Sn doped TiO{sub 2} nanocrystalline powders have been investigated and compared using EDX, Raman spectroscopy, X-ray Photoelectron spectroscopy (XPS), and Transient Absorption spectroscopy (TAS). Surface free energy states distributions were probed using Electrochemical Impedance spectroscopy (EIS) on Dye Sensitized Solar Cells (DSSC) based on the doped TiO{sub 2} photoanodes. Raman and XPS Ti2p{sub 3/2} peak shifts and broadening showed that the concentration of defects were in the order: Cu doped TiO{sub 2} > Fe doped TiO{sub 2} > Sn doped TiO{sub 2} > pure TiO{sub 2}. Nanosecond laser flash photolysis of Fe and Cu doped TiO{sub 2} indicated slower transient decay kinetics than that of Sn doped TiO{sub 2} or pure TiO{sub 2}. A broad absorption peak and fast