WorldWideScience

Sample records for cupc copper phthalocyanine

  1. Hindered rotation of a copper phthalocyanine molecule on C60 : Experiments and molecular mechanics calculations

    NARCIS (Netherlands)

    Fendrich, M.; Wagner, Th.; Stöhr, M.; Möller, R.

    2006-01-01

    If copper phthalocyanine (CuPc) molecules are deposited on a Au(111) surface covered with a monolayer of C60, the molecules are found to adsorb individually onto the close-packed layer of C60. As the adsorption site of the CuPc is not symmetric with respect to the underlying C60 layer, the CuPc mole

  2. Hindered rotation of a copper phthalocyanine molecule on C60 : Experiments and molecular mechanics calculations

    NARCIS (Netherlands)

    Fendrich, M.; Wagner, Th.; Stöhr, M.; Möller, R.

    2006-01-01

    If copper phthalocyanine (CuPc) molecules are deposited on a Au(111) surface covered with a monolayer of C60, the molecules are found to adsorb individually onto the close-packed layer of C60. As the adsorption site of the CuPc is not symmetric with respect to the underlying C60 layer, the CuPc

  3. Copper phthalocyanine and metal free phthalocyanine bulk heterojunction photodetector

    Energy Technology Data Exchange (ETDEWEB)

    Farooq, Amjad, E-mail: amjad.farooq1212@hotmail.com [Wah Engineering College, University of Wah, Wah Cantt. 47040 (Pakistan); GIK Institute of Engineering Sciences and Technology, Topi 23640, Swabi (Pakistan); Karimov, Kh.S. [GIK Institute of Engineering Sciences and Technology, Topi 23640, Swabi (Pakistan); Physical Technical Institute, Aini St. 299/1, Dushanbe 734063 (Tajikistan); Ahmed, Nisar; Ali, Taimoor [GIK Institute of Engineering Sciences and Technology, Topi 23640, Swabi (Pakistan); Khalid Alamgir, M. [National Institute of Vacuum Science and Technology, NCP complex, Islamabad 44000 (Pakistan); Usman, Muhammad [Experimental Physics Laboratories, National Centre for Physics, Quaid-i-Azam University, Islamabad 44000 (Pakistan)

    2015-01-15

    In this study we present the dependence of electrical properties of copper phthalocyanine (CuPc) and metal free phthalocyanine (H{sub 2}Pc) bulk heterojunction structure under different illumination levels. To fabricate the device on ITO coated glass substrate the bulk heterojunction thin film of CuPc and H{sub 2}Pc with thickness varying from 100 nm to 300 nm are deposited by thermal evaporator. Aluminum thin film was deposited by thermal evaporation as a top contact. The optical properties of the fabricated device are investigated using UV–vis spectroscopy. The current-voltage characteristics in dark and under illumination show that the device is sensitive towards visible light. The absorption spectrum describes its photo sensitivity in the range of wavelength from 200 nm to 850 nm. Simulation of current-intensity of light curve is carried out and experimental results are found in good agreement with simulated ones.

  4. Dynamics of copper-phthalocyanine molecules on Au/Ge(001)

    NARCIS (Netherlands)

    Sotthewes, K.; Heimbuch, R.U.; Zandvliet, H.J.W.

    2015-01-01

    Spatially resolved current-time scanning tunneling spectroscopy combined with current-distance spectroscopy has been used to characterize the dynamic behavior of copper-phthalocyanine (CuPc) molecules adsorbed on a Au-modified Ge(001) surface. The analyzed CuPc molecules are adsorbed in a “molecular

  5. Dynamics of copper-phthalocyanine molecules on Au/Ge(001)

    NARCIS (Netherlands)

    Sotthewes, Kai; Heimbuch, Rene; Zandvliet, Henricus J.W.

    2015-01-01

    Spatially resolved current-time scanning tunneling spectroscopy combined with current-distance spectroscopy has been used to characterize the dynamic behavior of copper-phthalocyanine (CuPc) molecules adsorbed on a Au-modified Ge(001) surface. The analyzed CuPc molecules are adsorbed in a “molecular

  6. Ab initio electronic structure and correlations in pristine and potassium-doped molecular crystals of copper phthalocyanine

    NARCIS (Netherlands)

    Giovannetti, Gianluca; Brocks, Geert; Brink, van den Jeroen

    2008-01-01

    We investigate the effect that potassium intercalation has on the electronic structure of copper phthalocyanine (CuPc) molecular crystals by means of ab initio density functional calculations. Pristine CuPc (in its alpha and beta structures) is found to be an insulator containing local magnetic mome

  7. Ab initio electronic structure and correlations in pristine and potassium-doped molecular crystals of copper phthalocyanine

    NARCIS (Netherlands)

    Giovannetti, G.; Brocks, G.; van den Brink, J.

    2008-01-01

    We investigate the effect that potassium intercalation has on the electronic structure of copper phthalocyanine (CuPc) molecular crystals by means of ab initio density functional calculations. Pristine CuPc (in its alpha and beta structures) is found to be an insulator containing local magnetic

  8. Ab initio electronic structure and correlations in pristine and potassium-doped molecular crystals of copper phthalocyanine

    NARCIS (Netherlands)

    Giovannetti, G.; Brocks, G.; van den Brink, J.

    2008-01-01

    We investigate the effect that potassium intercalation has on the electronic structure of copper phthalocyanine (CuPc) molecular crystals by means of ab initio density functional calculations. Pristine CuPc (in its alpha and beta structures) is found to be an insulator containing local magnetic mome

  9. Energy level alignment at the methylammonium lead iodide/copper phthalocyanine interface

    Directory of Open Access Journals (Sweden)

    Shi Chen

    2014-08-01

    Full Text Available The energy level alignment at the CH3NH3PbI3/copper phthalocyanine (CuPc interface is investigated by X-ray photoelectron spectroscopy (XPS and ultraviolet photoelectron spectroscopy (UPS. XPS reveal a 0.3 eV downward band bending in the CuPc film. UPS validate this finding and further reveal negligible interfacial dipole formation – verifying the viability of vacuum level alignment. The highest occupied molecular orbital of CuPc is found to be closer to the Fermi level than the valance band maximum of CH3NH3PbI3, facilitating hole transfer from CH3NH3PbI3 to CuPc. However, subsequent hole extraction from CuPc may be impeded by the downward band bending in the CuPc layer.

  10. Energy level alignment at the methylammonium lead iodide/copper phthalocyanine interface

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Shi; Goh, Teck Wee; Sum, Tze Chien, E-mail: Alfred@ntu.edu.sg, E-mail: Tzechien@ntu.edu.sg [Division of Physics and Applied Physics, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore 637371 (Singapore); Sabba, Dharani; Chua, Julianto; Mathews, Nripan [Energy Research Institute @NTU (ERI-N), Research Techno Plaza, X-Frontier Block, Level 5, 50 Nanyang Drive, Singapore 637553 (Singapore); School of Materials Science and Engineering, Nanyang Technological University, Nanyang Avenue, Singapore 639798 (Singapore); Huan, Cheng Hon Alfred, E-mail: Alfred@ntu.edu.sg, E-mail: Tzechien@ntu.edu.sg [Division of Physics and Applied Physics, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore 637371 (Singapore); Institute of High Performance Computing, 1 Fusionopolis Way, #16–16 Connexis, Singapore 138632 (Singapore)

    2014-08-01

    The energy level alignment at the CH{sub 3}NH{sub 3}PbI{sub 3}/copper phthalocyanine (CuPc) interface is investigated by X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS). XPS reveal a 0.3 eV downward band bending in the CuPc film. UPS validate this finding and further reveal negligible interfacial dipole formation – verifying the viability of vacuum level alignment. The highest occupied molecular orbital of CuPc is found to be closer to the Fermi level than the valance band maximum of CH{sub 3}NH{sub 3}PbI{sub 3}, facilitating hole transfer from CH{sub 3}NH{sub 3}PbI{sub 3} to CuPc. However, subsequent hole extraction from CuPc may be impeded by the downward band bending in the CuPc layer.

  11. Copper-phthalocyanine encapsulated into zeolite-Y with high Si/Al: An EPR study

    Science.gov (United States)

    Yahiro, Hidenori; Kimoto, Kunihiro; Yamaura, Hiroyuki; Komaguchi, Kenji; Lund, Anders

    2005-10-01

    Copper (II) phthalocyanine (CuPc) molecules encapsulated into zeolite-Y with Si/Al ratios of 2.7 and 410 were prepared by an in situ synthesis and characterized by UV-Vis and electron paramagnetic resonance (EPR) spectroscopies. Resolved Cu-hyperfine and N-superhyperfine structures were observed in the EPR spectrum of CuPc encapsulated into zeolite-Y with a high Si/Al ratio. UV-Vis and EPR studies as well as theoretical calculations suggest that the encapsulated CuPc molecule was distorted in zeolite-Y with keeping of the square-planar symmetry around the center copper (II) ion.

  12. Copper Phthalocyanine Catalysis to Oxidation of Adrenaline by Oxygen and Its Application in Adrenaline Detection

    Institute of Scientific and Technical Information of China (English)

    HUANG Jun; LI Mingtian; TANG Yan; FANG Hua; DING Liyun

    2008-01-01

    The oxidation of adrenaline by dioxygen using copper phthalocyanine (CuPc) as the catalyzer was studied. CuPc has the optimal catalytic pH of 8.0 and the optimal catalytic temperature of 55 ℃. It also has good storage and operation stability. The fiber optic adrenaline biosensor based on CuPc catalysis and fluorescence quenching was fabricated and studied. This sensor has the detection range of 7.0×10-5 -1.5×10-4 mol/L, the response time of 4 min, good reproducibility and stability.

  13. [Structural characterization of copper-phthalocyanine thin solid films by FTIR spectroscopy].

    Science.gov (United States)

    Ding, H; Zhang, Y; Chen, W; Xi, S

    1997-04-01

    The structure of tris- (2, 4-di-t-amylpheoxy) - (8-quinolinoxy) copper phthalocyanine (CuPc) thin solid films has been characterized by Fourier transform infrared (FTIR) transmission, polarized transmission and reflection absorption (RA) spectroscopy. The following conclusions can be obtained from the above measurements: (1)in LB films, the hydrocarbon chains of CuPc are in hexagonal or pseudohexagonal subcell packing, the CH2 asymmetric vibrational vector is oriented with respect to the substrate surface and the RA spectroscopy can distinguish the two CH2 streching modes of benzene cycle; (2)in sublimed films, the molecules of CuPc are out of order.

  14. Binary molecular layers of C-60 and copper phthalocyanine on Au(111) : Self-organized nanostructuring

    NARCIS (Netherlands)

    Stöhr, Meike; Wagner, Thorsten; Gabriel, Markus; Weyers, Bastian; Möller, Rolf

    2001-01-01

    The binary molecular system of C-60 and copper phthalocyanine(CuPc) molecules has been investigated by scanning tunneling microscopy (STM) at room temperature and at 50 K. As substrate Au(111) was chosen. When C-60 and CuPc molecules are sequentially deposited, it is found that well-ordered domains

  15. Electronic structure of copper phthalocyanine : An experimental and theoretical study of occupied and unoccupied levels

    NARCIS (Netherlands)

    Evangelista, Fabrizio; Carravetta, Vincenzo; Stefani, Giovanni; Jansik, Branislav; Alagia, Michele; Stranges, Stefano; Ruocco, Alessandro

    2007-01-01

    An experimental and theoretical study of the electronic structure of copper phthalocyanine (CuPc) molecule is presented. We performed x-ray photoemission spectroscopy (XPS) and photoabsorption [x-ray absorption near-edge structure (XANES)] gas phase experiments and we compared the results with self-

  16. Binary molecular layers of C-60 and copper phthalocyanine on Au(111) : Self-organized nanostructuring

    NARCIS (Netherlands)

    Stöhr, Meike; Wagner, Thorsten; Gabriel, Markus; Weyers, Bastian; Möller, Rolf

    The binary molecular system of C-60 and copper phthalocyanine(CuPc) molecules has been investigated by scanning tunneling microscopy (STM) at room temperature and at 50 K. As substrate Au(111) was chosen. When C-60 and CuPc molecules are sequentially deposited, it is found that well-ordered domains

  17. Electronic structure of copper phthalocyanine : An experimental and theoretical study of occupied and unoccupied levels

    NARCIS (Netherlands)

    Evangelista, Fabrizio; Carravetta, Vincenzo; Stefani, Giovanni; Jansik, Branislav; Alagia, Michele; Stranges, Stefano; Ruocco, Alessandro

    2007-01-01

    An experimental and theoretical study of the electronic structure of copper phthalocyanine (CuPc) molecule is presented. We performed x-ray photoemission spectroscopy (XPS) and photoabsorption [x-ray absorption near-edge structure (XANES)] gas phase experiments and we compared the results with

  18. Electronic structure of copper phthalocyanine : An experimental and theoretical study of occupied and unoccupied levels

    NARCIS (Netherlands)

    Evangelista, Fabrizio; Carravetta, Vincenzo; Stefani, Giovanni; Jansik, Branislav; Alagia, Michele; Stranges, Stefano; Ruocco, Alessandro

    2007-01-01

    An experimental and theoretical study of the electronic structure of copper phthalocyanine (CuPc) molecule is presented. We performed x-ray photoemission spectroscopy (XPS) and photoabsorption [x-ray absorption near-edge structure (XANES)] gas phase experiments and we compared the results with self-

  19. Binary molecular layers of C-60 and copper phthalocyanine on Au(111) : Self-organized nanostructuring

    NARCIS (Netherlands)

    Stöhr, Meike; Wagner, Thorsten; Gabriel, Markus; Weyers, Bastian; Möller, Rolf

    2001-01-01

    The binary molecular system of C-60 and copper phthalocyanine(CuPc) molecules has been investigated by scanning tunneling microscopy (STM) at room temperature and at 50 K. As substrate Au(111) was chosen. When C-60 and CuPc molecules are sequentially deposited, it is found that well-ordered domains

  20. Corrections to the density-functional theory electronic spectrum: Copper phthalocyanine

    DEFF Research Database (Denmark)

    Vazquez, Hector; Jelinek, P.; Brandbyge, Mads;

    2009-01-01

    A method for improving the electronic spectrum of standard Density-Functional Theory (DFT) calculations (i.e., LDA or GGA approximations) is presented, and its application is discussed for the case of the copper phthalocyanine (CuPc) molecule. The method is based on a treatment of exchange and co...

  1. Nucleation and growth of copper phthalocyanine aggregates deposited from solution on planar surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Ghani, Fatemeh [Department of Theory & Bio-Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1 Golm, 14476 Potsdam (Germany); Gojzewski, Hubert, E-mail: hubert.gojzewski@put.poznan.pl [Department of Theory & Bio-Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1 Golm, 14476 Potsdam (Germany); Institute of Physics, Poznan University of Technology, Piotrowo 3, 60-965 Poznan (Poland); Riegler, Hans [Department of Theory & Bio-Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1 Golm, 14476 Potsdam (Germany)

    2015-10-01

    Graphical abstract: - Highlights: • Copper phthalocyanine deposited on planar surfaces by 3 solution process methods. • Aggregate morphology examined for coverage extending over 3 orders of magnitude. • Morphologies vary from small individual domains to mesh-like multilayers. • Nucleation and growth model explains the observed deposit morphologies. - Abstract: Copper phthalocyanine (CuPc) dissolved in trifluoroacetic acid (TFA) is deposited on solid SiO{sub 2} surfaces by solvent evaporation. The deposited CuPc aggregates are investigated by atomic force microscopy (AFM). The CuPc deposits were prepared by spin casting, dip coating, and spray deposition. Depending on the amount of deposited CuPc the aggregate morphology ranges from small individual domains to mesh-like multilayers. Each domain/layer consists of many parallel stacks of CuPc molecules with the square, plate-like molecules piled face-wise within each stack. The parallel stacks are attached sideways (i.e., edgewise attachment molecularly) to the substrate forming “nanoribbons” with uniform thickness of about 1 nm and varying width. The thickness reflects the length of a molecular edge, the width the number of stacks. A nucleation and growth model is presented that explains the observed aggregate and multilayer morphologies as result of the combination of nucleation, transport processes and a consequence of the anisotropic intermolecular interactions due to the shape of the CuPc molecule.

  2. Graphene wrapped Copper Phthalocyanine nanotube: Enhanced photocatalytic activity for industrial waste water treatment

    Science.gov (United States)

    Mukherjee, Moumita; Ghorai, Uttam Kumar; Samanta, Madhupriya; Santra, Angshuman; Das, Gour P.; Chattopadhyay, Kalyan K.

    2017-10-01

    To improve the photocatalytic performance of metal phthalocyanine based catalyst, Copper Phthalocyanine (CuPc) functionalized reduced graphene oxide (RGO) nanocomposite has been synthesized through a simple chemical approach. The obtained product was characterized by X-ray diffraction technique (XRD), Fourier transform infrared (FTIR) spectroscopy, Ultraviolet-visible spectroscopy (UV-vis) and High resolution transmission electron microscopy (HRTEM). The photocatalytic activity of the RGO/CuPc nanocomposite was performed by the degradation of Rhodamine B (RhB) under visible light irradiation. The photocatalytic studies revealed that the RGO/CuPc nanocomposite exhibits much stronger catalytic behavior than the pristine CuPc nanotube. A plausible mechanism for the photodegradation of Rhodamine B (RhB) was suggested. The RGO wrapped CuPc nanotube composite materials offer great potential as active photocatalysts for degradation of organic pollutions in industrial waste water.

  3. Modelling copper-phthalocyanine/cobalt-phthalocyanine chains: towards magnetic quantum metamaterials.

    Science.gov (United States)

    Wu, Wei

    2014-07-23

    The magnetic properties of a theoretically designed molecular chain structure CuCoPc2, in which copper-phthalocyanine (CuPc) and cobalt-phthalocyanine (CoPc) alternate, have been investigated across a range of chain structures. The computed exchange interaction for the α-phase CuCoPc2 is ∼ 5 K (ferromagnetic), in strong contrast to the anti-ferromagnetic interaction recently observed in CuPc and CoPc. The computed exchange interactions are strongly dependent on the stacking angle but weakly on the sliding angle, and peak at 20 K (ferromagnetic). These ferromagnetic interactions are expected to arise from direct exchange with the strong suppression of super-exchange interaction. These first-principles calculations show that π-conjugated molecules, such as phthalocyanine, could be used as building blocks for the design of magnetic materials. This therefore extends the concept of quantum metamaterials further into magnetism. The resulting new magnetic materials could find applications in the studies such as organic spintronics.

  4. Effect of post deposition annealing on the performance of copper phthalocyanine based organic thin film transistor

    Science.gov (United States)

    Padma, N.; Sawant, Shilpa N.; Sen, Shaswati; Gupta, S. K.

    2013-02-01

    The electrical performance of copper phthalocyanine (CuPc) based OFETs on SiO2 dielectric was studied with and without post deposition annealing of CuPc films. Field effect mobility of holes and the drain current modulation (Ion/Ioff) was found to increase by one order for devices with annealed films as compared to that with as deposited film. This is attributed to well connected grains and increased crystallinity of CuPc film. Subthreshold slope (SS) was found to be reducing with increase in annealing temperature and was minimum for the device with CuPc film annealed at 225 °C, implying lesser traps affecting the mobility of charge carriers.

  5. Tuning carrier mobility without spin transport degrading in copper-phthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, S. W.; Wang, P.; Chen, B. B.; Zhou, Y. [National Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, 22 Hankou Road, Nanjing 210093 (China); Ding, H. F., E-mail: hfding@nju.edu.cn, E-mail: dwu@nju.edu.cn; Wu, D., E-mail: hfding@nju.edu.cn, E-mail: dwu@nju.edu.cn [National Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, 22 Hankou Road, Nanjing 210093 (China); Collaborative Innovation Center of Advanced Microstructures, Nanjing University, 22 Hankou Road, Nanjing 210093 (China)

    2015-07-27

    We demonstrate more than one order of magnitude of carrier mobility tuning for the copper-phthalocyanine (CuPc) without spin transport degrading in organic spin valve devices. Depending on the preparation conditions, organic spin valves with the CuPc film mobility of 5.78 × 10{sup −3} and 1.11 × 10{sup −4} cm{sup 2}/V s are obtained for polycrystalline and amorphous CuPc, respectively. Strikingly, the spin diffusion lengths are almost the same regardless of their mobilities that are ∼50 times different, which is in sharp contrast with previous prediction. These findings directly support that the spin relaxation in CuPc is dominated by the spin-orbit coupling.

  6. Dissolution of copper phthalocyanine and fabrication of its nano-structure film

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The mono-protonated and di-protonated forms of copper phthalocyanine (CuPc) were obtained by increasing concentrations of trifluoroacetic acid (TFA) solution to a fixed concentration of CuPc solutions. UV-Vis spectrum shows that the Q bands of these two derivatives split and shift to the red, which means successive protonation happened and caused the two derivatives to lose their symmetry. After the protonation step, the solubility of protonated CuPc in organic solvent increased 60 times. The CuPc film was fabricated by the electrophoretic deposition (EPD) method from the protonated CuPc dissolved in nitromethane containing TFA. Scanning electron microscopy (SEM) showed that the deposited CuPc film on the indium tin oxide (ITO) substrate is composed of thread-like nanobelts with diameters between 100 nm and 200 nm. Furthermore, the CuPc film is in α phase with stacking direction (b-axis) parallel to the substrate, which was detected by X-ray diffraction.

  7. Dissolution of copper phthalocyanine and fabrication of its nano-structure film

    Institute of Scientific and Technical Information of China (English)

    SU JinLi; XUE MinZhao; MA Ning; SHENG QiaoRong; ZHANG Qing; LIU YanGang

    2009-01-01

    The mono-protonated and di-protonated forms of copper phthalocyanine (CuPc) were obtained by increasing concentrations of trifluoroacetic acid (TFA) solution to a fixed concentration of CuPc solutions.UV-Vis spectrum shows that the Q bands of these two derivatives split and shift to the red,which means successive protonation happened and caused the two derivatives to lose their symmetry.After the protonation step,the solubility of protonated CuPc in organic solvent increased 60 times.The CuPc film was fabricated by the electrophoretic deposition (EPD) method from the protonated CuPc dissolved in nitromethane containing TFA.Scanning electron microscopy (SEM) showed that the deposited CuPc film on the indium tin oxide (ITO) substrate is composed of thread-like nanobelts with diameters between 100 nm and 200 nm.Furthermore,the CuPc film is in α phase with stacking direction (b-axis) parallel to the substrate,which was detected by X-ray diffraction.

  8. Femtosecond to nanosecond excited state dynamics of vapor deposited copper phthalocyanine thin films.

    Science.gov (United States)

    Caplins, Benjamin W; Mullenbach, Tyler K; Holmes, Russell J; Blank, David A

    2016-04-28

    Vapor deposited thin films of copper phthalocyanine (CuPc) were investigated using transient absorption spectroscopy. Exciton-exciton annihilation dominated the kinetics at high exciton densities. When annihilation was minimized, the observed lifetime was measured to be 8.6 ± 0.6 ns, which is over an order of magnitude longer than previous reports. In comparison with metal free phthalocyanine (H2Pc), the data show evidence that the presence of copper induces an ultrafast relaxation process taking place on the ca. 500 fs timescale. By comparison to recent time-resolved photoemission studies, this is assigned as ultrafast intersystem crossing. As the intersystem crossing occurs ca. 10(4) times faster than lifetime decay, it is likely that triplets are the dominant excitons in vapor deposited CuPc films. The exciton lifetime of CuPc thin films is ca. 35 times longer than H2Pc thin films, while the diffusion lengths reported in the literature are typically quite similar for the two materials. These findings suggest that despite appearing to be similar materials at first glance, CuPc and H2Pc may transport energy in dramatically different ways. This has important implications on the design and mechanistic understanding of devices where phthalocyanines are used as an excitonic material.

  9. Sensitization of TiO2 Photoelectrodes Using Copper Phthalocyanine for Hydrogen Production

    Directory of Open Access Journals (Sweden)

    Álvaro Realpe

    2015-08-01

    Full Text Available The effect of the photoelectrode sensitization with copper phthalocyanine (CuPc was studied by means of the absorption of this organometallic compound on the surface of TiO2 film. Infrared absorption spectra (FTIR analysis was used for characterization of CuPc thin film deposited, then, the hydrogen production was evaluated by exposure to a source of visible light and sunlight. The results showed activation of the photoelectrode in the visible region, and under sunlight the current flow in sensitized photoelectrode is higher than to non-sensitized photoelectrode.

  10. Study on catalytic oxidation of planar binuclear copper phthalocyanine on 2-mercaptoethanol

    Institute of Scientific and Technical Information of China (English)

    CHEN Wenxing; WEI Lili; WANG Jinqian; YAO Yuyuan; L(U) Shenshui; CHEN Shiliang

    2006-01-01

    Mononuclear copper phthalocyanine (CuPc) and binuclear copper phthalocyanine (Cu2Pc2) were synthesized by the phenylanhydride-urea route, and their catalytic oxidation activity on 2-mercaptoethanol was studied. Based on the experimental results, a catalytic mechanism of Cu2Pc2 on 2-mercaptoethanol has been proposed. Furthermore, the effects of pH, Cu2Pc2 concentration, and temperature on the catalytic oxidation activity were evaluated. The results showed that CuPc has no catalytic activity, while Cu2Pc2 has high catalytic oxidation activity towards 2-mercaptoethanol with the optimal activity at pH 11. The reaction can further be enhanced by increasing Cu2Pc2 concentration and temperature, due to its endothermic characteristics.

  11. Structural and magnetic characterization of copper sulfonated phthalocyanine grafted onto treated polyethylene

    Science.gov (United States)

    Reznickova, A.; Kolska, Z.; Orendac, M.; Cizmar, E.; Sajdl, P.; Svorcik, V.

    2016-08-01

    This study focuses on high density polyethylene (HDPE) activated by Ar plasma treatment, subsequently grafted with copper sulfonated phthalocyanine (CuPc) especially pointing out to the surface and magnetic properties of those composites. Properties of pristine PE and their plasma treated counterparts were studied by different experimental techniques: X-ray photoelectron spectroscopy (XPS), UV-vis spectroscopy, zeta potential and by electron spin resonance (ESR). XPS analysis confirmed the successful grafting of phthalocyanine. The highest absorption was found for the sample grafted with bCuPc for 1 h. Electrokinetic analysis also confirmed the plasma treatment and also subsequent CuPc grafting influence significantly the surface chemistry and charge. These results correspond well with XPS determination. ESR studies confirmed the presence of CuPc grafted on HDPE. It was found, that grafting is mediated by magnetically inactive functional groups, rather than radicals. Magnetic properties of CuPc do not seem to change significantly after grafting CuPc on polyethylene surface.

  12. Sensing response of copper phthalocyanine salt dispersed glass with organic vapours

    Energy Technology Data Exchange (ETDEWEB)

    Ridhi, R.; Sachdeva, Sheenam; Saini, G. S. S.; Tripathi, S. K., E-mail: surya@pu.ac.in [Department of Physics, Center of Advanced Study in Physics, Panjab University, Chandigarh-160 014 (INDIA) Fax: +91-172-2783336; Tel.:+91-172-2544362 (India)

    2016-05-06

    Copper Phthalocyanine and other Metal Phthalocyanines are very flexible and tuned easily to modify their structural, spectroscopic, optical and electrical properties by either functionalizing them with various substituent groups or by replacing or adding a ligand to the central metal atom in the phthalocyanine ring and accordingly can be made sensitive and selective to various organic species or gaseous vapours. In the present work, we have dispersed Copper Phthalocyanine Salt (CuPcS) in sol-gel glass form using chemical route sol-gel method and studied its sensing mechanism with organic vapours like methanol and benzene and found that current increases onto their exposure with vapours. A variation in the activation energies was also observed with exposure of vapours.

  13. Chemical sensing of copper phthalocyanine sol-gel glass through organic vapors

    Energy Technology Data Exchange (ETDEWEB)

    Ridhi, R.; Gawri, Isha; Abbas, Saeed J.; Saini, G. S. S.; Tripathi, S. K. [Department of Physics, Center of Advanced Study in Physics, Panjab University, Chandigarh-160 014 (INDIA) Fax: +91-172-2783336; Tel.:+91-172-2544362 (India)

    2015-05-15

    The sensitivities of metallophthalocyanine to vapor phase electron donors has gained significance in many areas and disciplines due to their sensing properties and ease of operation. In the present study the interaction mechanism of organic vapors in Copper Phthalocyanine (CuPc) sol-gel glass has been studied. The interaction mechanism is affected by many factors like morphology, electrical or optical properties of film. CuPc sol-gel glass has been synthesized using chemical route sol-gel method. Its structural characterization was conducted using XRD and the amorphous nature of the silicate glass was observed with characteristic α polymorph phase of CuPc at around 6.64° with 13.30Å interplanar spacing. The size of the particle as determined using Debbye Scherre’s formula comes out around 15.5 nm. The presence of α phase of CuPc was confirmed using FTIR with the appearance of crystal parameter marker band at 787 cm-1. Apart from this A2u and Eu symmetry bands of CuPc have also been observed. The UV absorption spectrum of CuPc exhibits absorption peaks owing to π→ π* and n→ π* transitions. A blue shift in the prepared CuPc glass has been observed as compared to the dopant CuPc salt indicating increase of band gap. A split in B (Soret) band and Q band appears as observed with the help of Lorentzian fitting. CuPc sol gel glass has been exposed with chemical vapors of Methanol, Benzene and Bromine individually and the electrical measurements have been carried out. These measurements show the variation in conductivity and the interaction mechanism has been analyzed.

  14. Change spectroscopic studies and optimization electrical properties of PVP/PEO doped copper phthalocyanines

    Energy Technology Data Exchange (ETDEWEB)

    Ragab, H.M., E-mail: yara20092009@yahoo.com [Department of Physics, Faculty of Science, Al-Azhar University, Girls Branch, Cairo 11754 (Egypt); Basic Science Department, Faculty of Preparatory Year, Hail University (Saudi Arabia); Ahmad, F.; Radwan, Sh.N. [Department of Physics, Faculty of Science, Al-Azhar University, Girls Branch, Cairo 11754 (Egypt)

    2016-12-01

    Composite films of polyvinyl pyrrolidone and Polyethylene oxide (PVP/PEO) blend doped with 1, 4 and 12 wt% of copper Phthalocyanines (CuPc) were prepared by casting method. The samples were studied using different techniques. The X-ray (XRD) revealed average crystallite size and X-ray intensity decrease at 1 CuPc %; this implies to an increase on the degree of amorphousity, then increase at CuPc >1%. The change in both the intensity and position of some absorption peaks of the blend with CuPc content were observed in Fourier transform infrared (FTIR) spectroscopy suggest the complexation of polymer blend. The UV–Vis spectroscopy revealed that the optical band gap decreases as well as band tail width increases with increasing CuPc concentration. It may be reflect the role of CuPc in modifying the electronic structure of the polymeric matrix. The charge carrier concentration is responsible for conductivity improvement in electrolytes rather than the mobility.

  15. Change spectroscopic studies and optimization electrical properties of PVP/PEO doped copper phthalocyanines

    Science.gov (United States)

    Ragab, H. M.; Ahmad, F.; Radwan, Sh. N.

    2016-12-01

    Composite films of polyvinyl pyrrolidone and Polyethylene oxide (PVP/PEO) blend doped with 1, 4 and 12 wt% of copper Phthalocyanines (CuPc) were prepared by casting method. The samples were studied using different techniques. The X-ray (XRD) revealed average crystallite size and X-ray intensity decrease at 1 CuPc %; this implies to an increase on the degree of amorphousity, then increase at CuPc >1%. The change in both the intensity and position of some absorption peaks of the blend with CuPc content were observed in Fourier transform infrared (FTIR) spectroscopy suggest the complexation of polymer blend. The UV-Vis spectroscopy revealed that the optical band gap decreases as well as band tail width increases with increasing CuPc concentration. It may be reflect the role of CuPc in modifying the electronic structure of the polymeric matrix. The charge carrier concentration is responsible for conductivity improvement in electrolytes rather than the mobility.

  16. Dynamics of copper-phthalocyanine molecules on Au/Ge(001)

    Energy Technology Data Exchange (ETDEWEB)

    Sotthewes, K.; Heimbuch, R.; Zandvliet, H. J. W. [Physics of Interfaces and Nanomaterials, MESA" + Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500AE Enschede (Netherlands)

    2015-10-07

    Spatially resolved current-time scanning tunneling spectroscopy combined with current-distance spectroscopy has been used to characterize the dynamic behavior of copper-phthalocyanine (CuPc) molecules adsorbed on a Au-modified Ge(001) surface. The analyzed CuPc molecules are adsorbed in a “molecular bridge” configuration, where two benzopyrrole groups (lobes) are connected to a Au-induced nanowire, whereas the other two lobes are connected to the adjacent nanowire. Three types of lobe configurations are found: a bright lobe, a dim lobe, and a fuzzy lobe. The dim and fuzzy lobes exhibit a well-defined switching behavior between two discrete levels, while the bright lobe shows a broad oscillation band. The observed dynamic behavior is induced by electrons that are injected into the LUMO+1 orbital of the CuPc molecule. By precisely adjusting the tip-molecule distance, the switching frequency of the lobes can be tuned accurately.

  17. Intermixing behaviors of PCBM with CuPc on Au(1 1 1) surface

    Science.gov (United States)

    Masui, Akane; Sakaue, Hiroyuki; Takahagi, Takayuki; Suzuki, Hitoshi

    2016-09-01

    The behavior of phenyl-C61-butyric acid methyl ester (PCBM) and copper-phthalocyanine (CuPc) on a Au(1 1 1) surface was investigated using scanning tunneling microscopy (STM). When CuPc was deposited in addition to PCBM it entered and disturbed the regularly spaced double row superstructure of the PCBM molecules. PCBM intermixed with CuPc to form a new square shaped superstructure that consisted of six to eight PCBM molecules with a CuPc molecule in its center. The intermixing of these materials that was observed indicated that they possessed an attractive interaction.

  18. Controllable preparation of copper phthalocyanine single crystal nano column and its chlorine gas sensing properties

    Directory of Open Access Journals (Sweden)

    Jianhong Zhao

    2016-09-01

    Full Text Available The unsubstituted copper phthalocyanine (CuPc single crystal nano columns were fabricated for the first time as chlorine (Cl2 gas sensors in this paper. The nano columns of CuPc have been prepared on different substrates via template-free physical vapor deposition (PVD approach. The growth mechanism of CuPc nano column on quartz was explored and the same condition used on other substrates including glass, sapphire (C-plane, M-plane, R-plane, Si and SiO2/Si came to a same conclusion, which confirmed that the aligned growth of CuPc nano column is not substrate-dependent. And then the CuPc nano column with special morphology was integrated as in-situ sensor device which exhibits high sensitivity and selectivity towards Cl2 at room temperature with a minimum detection limit as low as 0.08 ppm. The response of sensor was found to increase linearly (26∼659% with the increase for Cl2 within concentration range (0.08∼4.0ppm. These results clearly demonstrate the great potential of the nano column growth and device integration approach for sensor device.

  19. Studies on structure and Raman spectroscopy of Ni-doped copper phthalocyanine thin films

    Energy Technology Data Exchange (ETDEWEB)

    Wang, XueYan, E-mail: wxyadeline@163.com; Zheng, JianBang; Qiao, Kai; Qu, JunRong; Cao, ChongDe

    2014-04-01

    Highlights: • CuPc films with and without Ni-doping were prepared in high vacuum chamber. • The morphology, crystallinity, crystallite dimension and optical properties of these mixed films changed gradually with the increase of proportion of Ni-doping, but CuPc still kept their original α-phase crystal. • Raman intensities of all the vibration modes in RRS are not enhanced in the same way but are enhanced selectively. • The amorphous nickel atoms clusters had a noticeable light absorption and reflectivity loss. - Abstract: Ni-doped copper phthalocyanine (CuPc) organic films with different mixing ratios were prepared in high vacuum (HV) chamber. The results of AFM, XRD, UV–vis and Raman spectroscopy indicated that the surface morphologies of the films were found to be flater and the structures of the CuPc films still kept their original α-phase crystal, with only the crystallinity or crystallite sizes being changed and the versatile structure or charge transport being modified with the increase of Ni-doping ratios. Moreover, 514 nm-visible-light-excited normal Raman spectra (NRS), 325 nm-ultraviolet-excited and 633 nm-excited resonance Raman spectra (RRS) were analyzed by comparison and by density functional theory (DFT) calculations of the amorphous nickel atoms clusters, confirming that there were no chemical changes between CuPc molecules and nickel atoms; and the amorphous nickel atoms clusters had a noticeable light absorption loss, offering us an insightful structural understanding of the Raman effect of the different concentrations of Ni-doped CuPc films.

  20. Effect of annealing on bulk heterojunction organic solar cells based on copper phthalocyanine and perylene derivative

    KAUST Repository

    Kim, Inho

    2012-02-01

    We investigated the effects of annealing on device performances of bulk heterojunction organic solar cells based on copper phthalocyanine (CuPc) and N,N′-3,4,9,10-perylenetetracarboxylic diimide (PTCDI-C6). Blended films of CuPc and PTCDI-C6 with annealing at elevated temperature were characterized by measuring optical absorption, photoluminescence, and X-ray diffraction. Enhanced molecular ordering and increments in domain sizes of donor and acceptor for the blended films were observed, and their influences on device performances were discussed. Annealing led to substantial improvements in photocurrent owing to enhanced molecular ordering and formation of percolation pathways. © 2011 Elsevier B.V. All rights reserved.

  1. Effect of annealing copper phthalocyanine on the performance of interdigitated bulk-heterojunction organic photovoltaic cells

    Science.gov (United States)

    Wang, N. N.; Yu, J. S.; Yuan, Z. L.; Jiang, Y. D.

    2012-05-01

    Organic photovoltaic (OPV) cells with improved efficiency using thermal annealing-induced nanostructured copper phthalocyanine as a donor layer were fabricated. A power conversion efficiency of 1.47% in the OPV cell with interdigitated CuPc/C60 bulk heterojunction has been obtained under AM 1.5 solar illumination at an intensity of 100 mW/cm2, which is higher than 0.63% of CuPc/C60 planar cell. Through varying the annealing temperature of CuPc films, the influence of interface morphology and crystallinity of CuPc films on the performance of OPV cells was systematically studied. Field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD) and spectrophotometry were used to characterize the CuPc films. The results showed that at an optimal annealing temperature, the crystalline nature and vertical orientation of nanostructured CuPc have been modified, which can facilitate the separation of interfacial electron-hole pairs and charge carrier transport to electrodes.

  2. Field-effect transistor chemical sensors of single nanoribbon of copper phthalocyanine

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Copper phthalocyanine (CuPc) nanoribbon field-effect transistors were implemented as chemical sensors. They showed fast response and high reversibility in the detection of the tetrahydrofuran atmosphere at room temperature. The drain current of the field-effect transistor sensor decreased from 6.7 to 0.2 nA when the transistor was measured under the tetrahydrofuran atmosphere. The sensor was self-refreshable in a few minutes. These results demonstrate that the organic single crystalline nanoribbon transistors could effectively act as chemical sensors.

  3. Preparation and operation characteristics of organic semiconductor transistor using thin film Al gate and copper phthalocyanine

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The organic static induction transistors (OSITs) are fabricated by the method of evaporating and plating in a vacuum with copper phthalocyanine (CuPc) dye, and has a five layered structure of Au/CuPc/AL/CuPc/Au. The experiment reveals that OSITs have obtained a low driving voltage, high current density and high switch speed such as IDs = 1.2 × 10-6A/mm2 , and the degree of 1 000 Hz. The OSITs have excellent operation characteristics of typical static induction transistors.

  4. Influence of heat treatment on indium-tin-oxide anodes and copper phthalocyanine hole injection layers in organic light-emitting diodes

    Energy Technology Data Exchange (ETDEWEB)

    Fenenko, Larysa [Department of Photonics Materials Science, Chitose Institute of Science and Technology (CIST), 758-65 Bibi, Chitose, Hokkaido 066-8655 (Japan) and Department of Optoelectronics, V. E. Lashkaryov Institute of Semiconductor Physics of NASU, 41 Nauky Ave., Kyiv 03128 (Ukraine) and Center for Future Chemistry, Kyushu University, 744 Motooka, Nishi, Fukuoka 819-0395 (Japan)]. E-mail: adachi@cstf.kyushu-u.ac.jp; Adachi, Chihaya [Department of Photonics Materials Science, Chitose Institute of Science and Technology (CIST), 758-65 Bibi, Chitose, Hokkaido 066-8655 (Japan); Center for Future Chemistry, Kyushu University, 744 Motooka, Nishi, Fukuoka 819-0395 (Japan)

    2007-04-09

    Modifications of indium-tin-oxide (ITO) and copper phthalocyanine (CuPc) layers by heat treatment aimed at lowering driving voltage in organic light-emitting diodes (OLEDs) are examined. Significant changes were observed in the surface morphology and carrier injection properties of ITO and CuPc layers after annealing at T = 250 deg. C for 0-60 min in a glove box. In the case of ITO annealing, although the ITO work function gradually decreased and the surface of the ITO layer became smoother than that of an unannealed ITO layer, we observed an appreciable decrease in the driving voltage with an increase in annealing time. In the case of CuPc annealing, on the other hand, we observed deterioration of the OLED's characteristics. All devices demonstrated an increase in driving voltage due to the pronounced crystallization of the CuPc layer.

  5. Molecular orientation of copper phthalocyanine thin films on different monolayers of fullerene on SiO{sub 2} or highly oriented pyrolytic graphite

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Chenggong; Wang, Congcong [Department of Physics and Astronomy, University of Rochester, Rochester, New York 14627 (United States); Liu, Xiaoliang [Institute for Super-microstructure and Ultrafast Process in Advanced Materials (ISUPAM), Central South University, Changsha, Hunan 410083 (China); Xu, Xumei; Li, Youzhen [School of Physics and Electronics, Central South University, Changsha, Hunan 410083 (China); Xie, Fangyan [Instrumental Analysis Center, Sun Yat-Sen University, Guangzhou 510275 (China); Gao, Yongli [Department of Physics and Astronomy, University of Rochester, Rochester, New York 14627 (United States); Institute for Super-microstructure and Ultrafast Process in Advanced Materials (ISUPAM), Central South University, Changsha, Hunan 410083 (China)

    2015-03-23

    The interface electronic structures of copper phthalocyanine (CuPc) have been studied using ultraviolet photoemission spectroscopy as different monolayers of C{sub 60} were inserted between CuPc and a SiO{sub 2} or highly ordered pyrolytic graphite (HOPG) substrate. The results show that CuPc has standing up configuration with one monolayer of C{sub 60} insertion on SiO{sub 2} while lying down on HOPG, indicating that the insertion layer propagates the CuPc-substrate interaction. Meanwhile, CuPc on more than one monolayers of C{sub 60} on different substrates show that the substrate orientation effect quickly vanished. Our study elucidates intriguing molecular interactions that manipulate molecular orientation and donor-acceptor energy level alignment.

  6. Comparison Studies of Dielectric and AC Conduction of PbPc and CuPc Thin Films

    Directory of Open Access Journals (Sweden)

    S. Sivamalar

    2012-08-01

    Full Text Available The thin film of Lead Phthalocyanine (PbPc and Copper Phthalocyanine (CuPc on glass are prepared by Vacuum deposition method. Deposition of PbPc and CuPc on pre-cleaned glass substrates under the pressure of 10-6 Torr are achieved by slowly varying current of 20 Volt. The rate of evaporation is properly controlled and maintained constant during all the evaporations. The thicknesses of the films are 150 nm, 300 nm and 450 nm on glass substrate. Dielectric and AC conduction studies of Lead Phthalocyanine and Cupper Phthalocyanine thin films have been studied. The variations of capacitance with frequency at different, permittivity with temperature, capacitance with temperature and ac conductance with frequency at different temperatures of PbPc and CuPc have been studied. The activation energies have been determined from the slope of 1000/T vs. log Gp curves at different frequencies (where Gp= -Eg/RT.

  7. Effect of polymer modification of SiO2 dielectric on the performance of copper phthalocyanine based organic thin film transistor

    Science.gov (United States)

    Padma, N.; Chauhan, A. K.; Sawant, Shilpa N.; Gupta, S. K.

    2012-06-01

    Effect of polystyrene (PS) modification of SiO2 dielectric on the performance of copper phthalocyanine (CuPc) based OFETs was studied. Field effect mobility of holes was found to increase by one order for polystyrene modified dielectric as compared to that on unmodified SiO2. This is attributed to well connected grains and increased crystallinity of CuPc film. Significantly reduced hysteresis was found in the devices with PS/SiO2 dielectric due to almost complete absence of hydroxyl groups at the dielectric/semiconductor interface and hence reduced trap sites.

  8. Scanning tunneling microscopy investigation of self-assembled CuPc/F16CuPc binary superstructures on graphite.

    Science.gov (United States)

    Huang, Yu Li; Li, Hui; Ma, Jing; Huang, Han; Chen, Wei; Wee, Andrew T S

    2010-03-01

    The self-assembly of the binary molecular system comprising copper(II) phthalocyanine (CuPc) and copper-hexadecafluoro-phthalocyanine (F(16)CuPc) on graphite has been investigated by in situ low-temperature scanning tunneling microscopy (LT-STM). The adsorption of this binary molecular system on graphite results in the formation of a well-ordered chessboardlike nanopattern. The in-plane molecular orientation of the guest CuPc molecules can be tuned by varying the coverage. At low coverage, the sparse CuPc molecules are randomly embedded in the host F(16)CuPc monolayer, possessing two different in-plane orientations; as the CuPc coverage increases, the in-plane molecular orientations of CuPc and F(16)CuPc become unidirectional and a highly ordered chessboardlike pattern forms. Molecular dynamic (MD) simulation results suggest that the selective and directional intermolecular hydrogen bonding determines the in-plane molecular orientation as well as the supramolecular packing arrangement.

  9. An improved performance of copper phthalocyanine OFETs with channel and source/drain contact modifications

    Science.gov (United States)

    Huanqin, Dang; Xiaoming, Wu; Xiaowei, Sun; Runqiu, Zou; Ruochuan, Zhang; Shougen, Yin

    2015-10-01

    We report an effective method to improve the performance of p-type copper phthalocyanine (CuPc) based organic field-effect transistors (OFETs) by employing a thin para-quaterphenyl (p-4p) film and simultaneously applying V2O5 to the source/drain regions. The p-4p layer was inserted between the insulating layer and the active layer, and V2O5 layer was added between CuPc and Al in the source-drain (S/D) area. As a result, the field-effect saturation mobility and on/off current ratio of the optimized device were improved to 5 × 10-2 cm2/(V·s) and 104, respectively. We believe that because p-4p could induce CuPc to form a highly oriented and continuous film, this resulted in the better injection and transport of the carriers. Moreover, by introducing the V2O5 electrode's modified layers, the height of the carrier injection barrier could be effectively tuned and the contact resistance could be reduced. Project supported by the National Natural Science Foundation of China (No. 60676051), the National High Technology Research and Development Program of China (No. 2013A A014201), the Scientific Developing Foundation of Tianjin Education Commission (No. 2011ZD02), the Key Science and Technology Support Program of Tianjin (No. 14ZCZDGX00006), and the Foundation of Key Discipline of Material Physics and Chemistry of Tianjin.

  10. Effect of film morphology on oxygen and water interaction with copper phthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Miller, Nicholas [California State University, Long Beach (CSULB); Gredig, Thomas [California State University, Long Beach (CSULB); Ivanov, Ilia N [ORNL

    2016-01-01

    Copper phthalocyanine (CuPc) films of thickness 25 nm and 100 nm were grown by thermal sublimation at 25 C, 150 C, and 250 C in order to vary morphology. Using a source-measure unit and a quartz crystal microbalance (QCM), we measured changes in electrical resistance and film mass in situ during exposure to controlled pulses of O2 and H2O vapor. Mass loading by O2 was enhanced by a factor of 5 in films deposited at 250 C, possibly due to the ~200 C CuPc transition which allows higher O2 mobility between stacked molecules. While gas/vapor sorption occurred over timescales of < 10 minutes, resistance change occurred over timescales > 1 hour, suggesting that mass change occurs by rapid adsorption at active surface sites, whereas resistive response is dominated by slow diffusion of adsorbates into the film bulk. Resistive response generally increases with film deposition temperature due to increased porosity associated with larger crystalline domains. The 25 nm thick films exhibit higher resistive response than 100 nm thick films after an hour of O2/H2O exposure due to the smaller analyte diffusion length required for reaching the film/electrode interface. We found evidence of decoupling of CuPc from the gold-coated QCM crystal due to preferential adsorption of O2/H2O molecules on gold, which is consistent with findings of other studies.

  11. Adsorption of Cu phthalocyanine on Pt modified Ge(001): A scanning tunneling microscopy study

    NARCIS (Netherlands)

    Saedi, Amirmehdi; Berkelaar, Robin P.; Kumar, Avijit; Poelsema, Bene; Zandvliet, Harold J.W.

    2010-01-01

    The adsorption configurations of copper phthalocyanine (CuPc) molecules on platinum-modified Ge(001) have been studied using scanning tunneling microscopy. After deposition at room temperature and cooling down to 77 K the CuPc molecules are still dynamic. However, after annealing at 550±50 K, the ad

  12. Adsorption of Cu phthalocyanine on Pt modified Ge(001): A scanning tunneling microscopy study

    NARCIS (Netherlands)

    Saedi, A.; Berkelaar, Robin P.; Kumar, Avijit; Poelsema, Bene; Zandvliet, Henricus J.W.

    2010-01-01

    The adsorption configurations of copper phthalocyanine (CuPc) molecules on platinum-modified Ge(001) have been studied using scanning tunneling microscopy. After deposition at room temperature and cooling down to 77 K the CuPc molecules are still dynamic. However, after annealing at 550±50 K, the

  13. Adsorption of Cu phthalocyanine on Pt modified Ge(001): A scanning tunneling microscopy study

    NARCIS (Netherlands)

    Saedi, A.; Berkelaar, Robin P.; Kumar, Avijit; Poelsema, Bene; Zandvliet, Henricus J.W.

    2010-01-01

    The adsorption configurations of copper phthalocyanine (CuPc) molecules on platinum-modified Ge(001) have been studied using scanning tunneling microscopy. After deposition at room temperature and cooling down to 77 K the CuPc molecules are still dynamic. However, after annealing at 550±50 K, the ad

  14. Influence of the morphology of the copper(II) phthalocyanine thin film on the performance of organic field-effect transistors

    Science.gov (United States)

    Xu, Jing; Liu, Xueqiang; Wang, Hailong; Hou, Wenlong; Zhao, Lele; Zhang, Haiquan

    2017-01-01

    Organic thin-film transistors (OTFTs) with high crystallization copper phthalocyanine (CuPc) active layers were fabricated. The performance of CuPc OTFTs was studied without and with treatment by Solvent Vapor Annealing on CuPc film. The values of the threshold voltage without and with solvent-vapor annealing are -17 V and -10.5 V respectively. The field-effect mobility values in saturation region of CuPc thin-film transistors without and with Solvent Vapor Annealing are 0.00027 cm2/V s and 0.0025 cm2/V s respectively. Meanwhile, the high crystallization of the CuPc film with a larger grain size and less grain boundaries can be observed by investigating the morphology of the CuPc active layer through scanning electron microscopy and X-ray diffraction. The experimental results showed the decreased of the resistance of the conducting channel, that led to a performance improvement of the OTFTs.

  15. Marine sponge skeleton photosensitized by copper phthalocyanine: A catalyst for Rhodamine B degradation

    Directory of Open Access Journals (Sweden)

    Norman Małgorzata

    2016-01-01

    Full Text Available We present a combined approach to photo-assisted degradation processes, in which a catalyst, H2O2 and UV irradiation are used together to enhance the oxidation of Rhodamine B (RB. The heterogeneous photocatalyst was made by the process of adsorption of copper phthalocyanine tetrasulfonic acid (CuPC onto purified spongin-based Hippospongia communis marine sponge skeleton (HcS. The product obtained, CuPC-HcS, was investigated by a variety of spectroscopic (carbon-13 nuclear magnetic resonance 13C NMR, Fourier transform infrared spectroscopy FTIR, energy-dispersive X-ray spectroscopy EDS and microscopic techniques (scanning electron microscopy SEM, fluorescent and optical microscopy, as well as thermal analysis. The study confirms the stable combination of the adsorbent and adsorbate. For a 10 mg/L RB solution, the percentage degradation reached 95% using CuPC-HcS as a heterocatalyst. The mechanism of RB removal involves adsorption and photodegradation simultaneously.

  16. The crystalline structure of copper phthalocyanine films on ZnO(1100).

    Science.gov (United States)

    Cruickshank, Amy C; Dotzler, Christian J; Din, Salahud; Heutz, Sandrine; Toney, Michael F; Ryan, Mary P

    2012-09-05

    The structure of copper phthalocyanine (CuPc) thin films (5-100 nm) deposited on single-crystal ZnO(1100) substrates by organic molecular beam deposition was determined from grazing-incidence X-ray diffraction reciprocal space maps. The crystal structure was identified as the metastable polymorph α-CuPc, but the molecular stacking was found to vary depending on the film thickness: for thin films, a herringbone arrangement was observed, whereas for films thicker than 10 nm, coexistence of both the herringbone and brickstone arrangements was found. We propose a modified structure for the herringbone phase with a larger monoclinic β angle, which leads to intrastack Cu-Cu distances closer to those in the brickstone phase. This structural basis enables an understanding of the functional properties (e.g., light absorption and charge transport) of (opto)electronic devices fabricated from CuPc/ZnO hybrid systems.

  17. Hybrid Solar Cell with TiO2 Film: BBOT Polymer and Copper Phthalocyanine as Sensitizer

    Directory of Open Access Journals (Sweden)

    Saptadip Saha

    2016-01-01

    Full Text Available An organic-inorganic hybrid solar cell was fabricated using Titanium dioxide (TiO2: 2,5-bis(5-tert-butyl-2-benzoxazolyl thiophene (BBOT film and Copper Phthalocyanine (CuPc as a sensitizer. BBOT was used in photodetector in other reported research works, but as per best of our knowledge, it was not implemented in solar cells till date. The blend of TiO2: BBOT blend was used to fabricate the film on ITO-coated glass and further a thin layer of CuPc was coated on the film. This was acted as photoanode and another ITO coated glass with a platinum coating was used as a counter electrode (cathode. An optimal blend of acetonitrile (solvent (50-100%, 1,3-dimethylimidazolium iodide (10-25%, iodine (2.5-10% and lithium iodide, pyridine derivative and thiocyanate was used as electrolytes in the hybrid solar cell. The different structural, optical and electrical characteristics were measured. The Hybrid solar cell showed a maximum conversion efficiency of 6.51%.

  18. Copper phthalocyanine growth on hydrogen-terminated Si(1 0 0) surfaces: Contrasted molecular arrangements revealed by X-ray photoelectron studies

    Energy Technology Data Exchange (ETDEWEB)

    Hamada, B. Ben; Akremi, A.; Arbi, I.; Menzli, S. [Universite de Carthage, Laboratoire de Physique des materiaux, equipe Surface et Interface (ESI), Faculte des Sciences de Bizerte, 7021 Jarzouna, Bizerte (Tunisia); Themlin, J.-M. [Aix-Marseille Univ, IM2NP, Avenue de l' Escadrille Normandie-Niemen, Case 142, F-13397 Marseille Cedex 20 (France); CNRS, IM2NP-UMR 7334, Marseille-Toulon (France); Porte, L., E-mail: louis.porte@im2np.fr [Aix-Marseille Univ, IM2NP, Avenue de l' Escadrille Normandie-Niemen, Case 142, F-13397 Marseille Cedex 20 (France); CNRS, IM2NP-UMR 7334, Marseille-Toulon (France); Chefi, C. [Universite de Carthage, Laboratoire de Physique des materiaux, equipe Surface et Interface (ESI), Faculte des Sciences de Bizerte, 7021 Jarzouna, Bizerte (Tunisia)

    2013-01-01

    Highlights: Black-Right-Pointing-Pointer Copper phthalocyanine growth on hydrogen-terminated Si(1 0 0) surfaces. Black-Right-Pointing-Pointer Molecular packing of CuPc onto hydrogen H-Si(1 0 0)-1 Multiplication-Sign 1 and H-Si(1 0 0)-2 Multiplication-Sign 1 surfaces. Black-Right-Pointing-Pointer Structure of CuPc monolayer determined by X-ray photoelectron diffraction. - Abstract: Copper phthalocyanine (CuPc) molecules have been deposited under ultra-high vacuum on two kinds of hydrogen-terminated silicon surfaces, namely the H-Si(1 0 0)-2 Multiplication-Sign 1 and H-Si(1 0 0)-1 Multiplication-Sign 1 surfaces. The chemical and structural properties of these interfaces were investigated in situ by X-ray photoelectron spectroscopy and X-ray photoelectron diffraction (XPD), and low-energy electron diffraction. Results from X-ray photoelectron diffraction shed light on the growth mechanism of CuPc on these two substrates. At one monolayer coverage the growth mode was characterized by the formation of crystalline 3D nano-islands. The molecular packing deduced from these studies appears very close to the one of the bulk CuPc phase. Interestingly, the growth mode appears significantly different for the two surfaces. Indeed, 3D islands are formed by molecules aligned in a standing manner in the case of H-Si(1 0 0)-2 Multiplication-Sign 1, and in a flat-lying manner in the case of H-Si(1 0 0)-1 Multiplication-Sign 1.

  19. Orienting the Microstructure Evolution of Copper Phthalocyanine as an Anode Interlayer in Inverted Polymer Solar Cells for High Performance.

    Science.gov (United States)

    Li, Zhiqi; Liu, Chunyu; Zhang, Xinyuan; Li, Shujun; Zhang, Xulin; Guo, Jiaxin; Guo, Wenbin; Zhang, Liu; Ruan, Shengping

    2017-09-20

    Recent advances in the interfacial modification of inverted-type polymer solar cells (PSCs) have resulted from controlling the surface energy of the cathode-modified layer (TiO2 or ZnO) to enhance the short-circuit current (Jsc) or optimizing the contact morphology of the cathode (indium tin oxide or fluorine-doped tin oxide) and active layer to increase the fill factor. Herein, we report that the performance enhancement of PSCs is achieved by incorporating a donor macromolecule copper phthalocyanine (CuPc) as an anode modification layer. Using the approach based on orienting the microstructure evolution, uniformly dispersed island-shaped CuPc spot accumulations are built on the top of PTB7:PC71BM blend film, leading to an efficient spectral absorption and photogenerated exciton splitting. The best power conversion efficiency of PSCs is increased up to 9.726%. In addition to the enhanced light absorption, the tailored anode energy level alignment and optimized boundary morphology by incorporating the CuPc interlayer boost charge extraction efficiency and suppress the interfacial molecular recombination. These results demonstrate that surface morphology induction through molecular deposition is an effective method to improve the performance of PSCs, which reveals the potential implications of the interlayer between the organic active layer and the electrode buffer layer.

  20. Energy level alignment at the Si(1 1 1)/RCA–SiO{sub 2}/copper(II) phthalocyanine ultra-thin film interface

    Energy Technology Data Exchange (ETDEWEB)

    Krzywiecki, Maciej, E-mail: maciej.krzywiecki@polsl.pl; Grządziel, Lucyna

    2014-08-30

    Graphical abstract: - Highlights: • The interface formation studies between CuPc and Si by photoemission methods. • Charge rearrangement detected at the inorganic/organic interface. • Existence of disordered/polarization layer at the initial stages of CuPc deposition. • Examined structures applicable for organic transistors development. - Abstract: The photoemission experimental techniques (i.e. ultraviolet photoelectron spectroscopy—UPS and X-ray photoelectron spectroscopy—XPS) were used to investigate the charge–rearrangement–related phenomena occuring at organic–inorganic semiconductor interface. Examined samples were copper phthalocyanine (CuPc) ultra-thin (up to 16 nm) layers deposited onto oxidized silicon Si(1 1 1) of n- and p-type of conductivity. The 1.3-nm-thick silicon oxide was prepared by means of RCA wet cleaning procedure. The analysis of the photoemission data (mainly UPS) suggested the existance of the polarization layer within first 3 nm of CuPc layer thickness. Basing on the UPS and XPS results the energy level diagrams of examined structures have been constructed. In present paper it is suggested that the existance of the polarization layer could be assigned to the disordered adsorption and continous molecular reorientation of the CuPc molecules during the interface formation process. In the terms of the lack of the charge transfer via substrate/organic overlayer interface and disordered adsorption the fluctuations of CuPc electronic parameters were detected. Moreover the ionization energy and the work function parameters of final CuPc layer were affected. The values were more consistent with those obtained for much thicker (over 500 nm) CuPc layers. Performed studies showed that contrary to CuPc layers deposited on native substrates (where the charge transfer via tunnelable oxide – determined as dipole effect – has been detected), the thicker RCA-prepared oxide seems to be non-tunnelable hence the possibility for Si(1 1 1

  1. Quantitative correlation between air induced changes of electronic parameters and morphological features of copper phthalocyanine thin film surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Grządziel, L., E-mail: Lucyna.Grzadziel@polsl.pl; Krzywiecki, M.

    2015-01-15

    In this work, utilizing fine-resolved photoemission yield spectroscopy (PYS) method, the set of electronic parameters of the space charge layer of 16 nm-copper phthalocyanine (CuPc) thin films deposited on n-type Si(111) substrate covered with modified SiO{sub 2} was determined after long term air exposure. The PYS investigation revealed that work function and surface band bending increased upon gas adsorption by 0.64 eV and 0.32 eV respectively for organic layer and surface dipole effect appeared as the shift in electron affinity of 0.32 eV. Obtained results were compared with photoemission data received for corresponding CuPc films on different types of silicon Si(111) substrate. Collected parameters were correlated with the morphological features of the CuPc's surfaces measured applying atomic force microscopy (AFM) ability. Results of compiled PYS and AFM studies indicated particular electronic tendency for oxidation processes for certain shapes of phthalocyanine crystallites. It may suggest that by manipulation of the initial films' morphology it would be possible to control the air stability of the CuPc-based electronic devices and their vulnerability to degradation processes. - Highlights: • PYS study of 16 nm-CuPc/RCA-SiO{sub 2}/n-Si(111) electronic properties after air exposure. • eV{sub s}, χ{sub s}, φ changes due to oxidation process compared to the other CuPc results. • Electronic parameters shift correlated with morphological features obtained by AFM.

  2. Nitrogen Dioxide Sensing Properties and Mechanism of Copper Phthalocyanine Film

    Institute of Scientific and Technical Information of China (English)

    QIU Cheng-Jun; DOU Yan-Wei; ZHAO Quan-Liang; QU Wei; YUAN Jie; SUN Yan-Mei; CAO Mao-Sheng

    2008-01-01

    Copper phthalocyanine film, a p-type organic semiconductor, is synthesized by vacuum sublimation and its surface morphology is characterized by SEM. A silicon-based copper phthalocyanine film gas sensor for NO2 detection is fabricated by MEMS technology. The results show that the resistance and sensitivity of copper phthalocyanine film decrease obviously as the NO2 concentration increases from Oppm to 100ppm. However, the sensitivity nearly keeps a constant of 0.158 between 30ppm and 70ppm. The best working temperature of the gas sensor is 90℃ for NO2 gas concentrations of 10ppm, 20ppm and 30ppm, which is much lower than that of general metal oxide gas sensor.

  3. Introduction of dielectric phthalocyanine copper into nano-structure Fe{sub 3}O{sub 4} for excellent microwave absorption

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Shihua; Meng, Fanbin; Jia, Kun, E-mail: jiakun@uestc.edu.cn; Liu, Xiaobo, E-mail: liuxb@uestc.edu.cn

    2015-05-15

    Phthalocyanine copper/magnetite (CuPc/Fe{sub 3}O{sub 4}) magnetic nanohybrids were synthesized from CuPc and FeCl{sub 3}·6H{sub 2}O via a facile solvent-thermal route. The nanohybrids were monodispersed solid nanospheres and the diameter can be adjusted by polymerization degree of CuPc. Importantly, the as-prepared CuPc/Fe{sub 3}O{sub 4} nanohybrids showed excellent microwave absorption properties due to the introduction of dielectric CuPc. A reflection loss ≤−5 dB from 10.0 GHz to 18.0 GHz with multi-frequency microwave absorption was exhibited, and the maximum reflection loss reached to −32.96 dB at 14.50 GHz. Furthermore, the microwave absorption property can be tuned easily by varying polymerization degree of CuPc and the layer thickness of the samples, respectively. Thus, these results offered a promising strategy for the fabrication of absorbents for thin-thickness and strong-absorption microwave absorbing materials with working frequencies adjustable over a wide range. - Highlights: • The diameter can be adjusted by varying polymerization degree of CuPc. • CuPc/Fe{sub 3}O{sub 4} exhibits a reflection loss ≤−5 dB from 10.0 to 18.0 GHz. • The nanohybrids exhibit multi-frequency microwave absorption from 10.0 to 18.0 GHz. • The maximum reflection loss reaches to −32.96 dB at 14.50 GHz. • The microwave absorption can be tuned by varying polymerization degree of CuPc.

  4. Phase and Texture of Solution-Processed Copper Phthalocyanine Thin Films Investigated by Two-Dimensional Grazing Incidence X-Ray Diffraction

    Directory of Open Access Journals (Sweden)

    Lulu Deng

    2011-07-01

    Full Text Available The phase and texture of a newly developed solution-processed copper phthalocyanine (CuPc thin film have been investigated by two-dimensional grazing incidence X-ray diffraction. The results show that it has β phase crystalline structure, with crystallinity greater than 80%. The average size of the crystallites is found to be about 24 nm. There are two different arrangements of crystallites, with one dominating the diffraction pattern. Both of them have preferred orientation along the thin film normal. Based on the similarities to the vacuum deposited CuPc thin films, the new solution processing method is verified to offer a good alternative to vacuum process, for the fabrication of low cost small molecule based organic photovoltaics.

  5. SEMICONDUCTOR DEVICES Low voltage copper phthalocyanine organic thin film transistors with a polymer layer as the gate insulator

    Science.gov (United States)

    Xueqiang, Liu; Weihong, Bi; Tong, Zhang

    2010-12-01

    Low voltage organic thin film transistors (OTFTs) were created using polymethyl-methacrylate-co g-lyciclyl-methacrylate (PMMA-GMA) as the gate dielectric. The OTFTs performed acceptably at supply voltages of about 10 V. From a densely packed copolymer brush, a leakage current as low as 2 × 10-8 A/cm2 was obtained. From the measured capacitance—insulator frequency characteristics, a dielectric constant in the range 3.9-5.0 was obtained. By controlling the thickness of the gate dielectric, the threshold voltage was reduced from -3.5 to -2.0 V. The copper phthalocyanine (CuPc) based organic thin film transistor could be operated at low voltage and 1.2 × 10-3 cm2/(V·s) mobility.

  6. Enhancement of photodetection characteristics of MoS2 field effect transistors using surface treatment with copper phthalocyanine

    Science.gov (United States)

    Pak, Jinsu; Jang, Jingon; Cho, Kyungjune; Kim, Tae-Young; Kim, Jae-Keun; Song, Younggul; Hong, Woong-Ki; Min, Misook; Lee, Hyoyoung; Lee, Takhee

    2015-11-01

    Recently, two-dimensional materials such as molybdenum disulfide (MoS2) have been extensively studied as channel materials for field effect transistors (FETs) because MoS2 has outstanding electrical properties such as a low subthreshold swing value, a high on/off ratio, and good carrier mobility. In this study, we characterized the electrical and photo-responsive properties of MoS2 FET when stacking a p-type organic copper phthalocyanine (CuPc) layer on the MoS2 surface. We observed that the threshold voltage of MoS2 FET could be controlled by stacking the CuPc layers due to a charge transfer phenomenon at the interface. Particularly, we demonstrated that CuPc/MoS2 hybrid devices exhibited high performance as a photodetector compared with the pristine MoS2 FETs, caused by more electron-hole pairs separation at the p-n interface. Furthermore, we found the optimized CuPc thickness (~2 nm) on the MoS2 surface for the best performance as a photodetector with a photoresponsivity of ~1.98 A W-1, a detectivity of ~6.11 × 1010 Jones, and an external quantum efficiency of ~12.57%. Our study suggests that the MoS2 vertical hybrid structure with organic material can be promising as efficient photodetecting devices and optoelectronic circuits.Recently, two-dimensional materials such as molybdenum disulfide (MoS2) have been extensively studied as channel materials for field effect transistors (FETs) because MoS2 has outstanding electrical properties such as a low subthreshold swing value, a high on/off ratio, and good carrier mobility. In this study, we characterized the electrical and photo-responsive properties of MoS2 FET when stacking a p-type organic copper phthalocyanine (CuPc) layer on the MoS2 surface. We observed that the threshold voltage of MoS2 FET could be controlled by stacking the CuPc layers due to a charge transfer phenomenon at the interface. Particularly, we demonstrated that CuPc/MoS2 hybrid devices exhibited high performance as a photodetector compared

  7. High-mobility solution-processed copper phthalocyanine-based organic field-effect transistors

    Directory of Open Access Journals (Sweden)

    Nandu B Chaure, Andrew N Cammidge, Isabelle Chambrier, Michael J Cook, Markys G Cain, Craig E Murphy, Chandana Pal and Asim K Ray

    2011-01-01

    Full Text Available Solution-processed films of 1,4,8,11,15,18,22,25-octakis(hexyl copper phthalocyanine (CuPc6 were utilized as an active semiconducting layer in the fabrication of organic field-effect transistors (OFETs in the bottom-gate configurations using chemical vapour deposited silicon dioxide (SiO2 as gate dielectrics. The surface treatment of the gate dielectric with a self-assembled monolayer of octadecyltrichlorosilane (OTS resulted in values of 4×10−2 cm2 V−1 s−1 and 106 for saturation mobility and on/off current ratio, respectively. This improvement was accompanied by a shift in the threshold voltage from 3 V for untreated devices to -2 V for OTS treated devices. The trap density at the interface between the gate dielectric and semiconductor decreased by about one order of magnitude after the surface treatment. The transistors with the OTS treated gate dielectrics were more stable over a 30-day period in air than untreated ones.

  8. Thermal Annealing Effect on Poly(3-hexylthiophene: Fullerene:Copper-Phthalocyanine Ternary Photoactive Layer

    Directory of Open Access Journals (Sweden)

    H. Derouiche

    2013-01-01

    Full Text Available We have fabricated poly(3-hexylthiophene (P3HT/copper phthalocyanine (CuPc/fullerene (C60 ternary blend films. This photoactive layer is sandwiched between an indium tin oxide (ITO/poly(3,4-ethylenedioxythiophene:poly(styrene sulfonate (PEDOT/PSS photoanode and a bathocuproine (BCP/aluminium photocathode. The thin films have been characterized by atomic force microscope (AFM and ultraviolet/visible spectroscopy in order to study the influence of P3HT doping on the morphological and optical properties of the photoactive layer. We have also compared the characteristics of three different organic solar cells: ITO/PEDOT:PSS/CuPc0.5:C600.5/BCP/Al and ITO/PEDOT:PSS/P3HT0.3:CuPc0.3:C600.4/BCP/Al with and without annealing. Both structures show good photovoltaic behaviour. Indeed, the incorporation of P3HT into CuPc:C60 thin film improves all the photovoltaic characteristics. We have also seen that thermal annealing significantly improves the optical absorption ability and stabilizes the organic solar cells making it more robust to chemical degradation.

  9. Self-assembled array of rectangular single-crystal microtubes of perchlorinated copper phthalocyanines

    Institute of Scientific and Technical Information of China (English)

    Dongwei Yan; n; Yitao Feng; Chunru Wang

    2013-01-01

    The rectangular microtubes array of perchlorinated copper phthalocyanines (Cl16CuPc), were synthesized by physical vapor deposition technique without using any template or catalyst. The synthesis process of the tubular structure is very simple, easy to control, and a little raw material is used. The morphology and crystal structure of the obtained samples were analyzed by means of scanning and transmission electron microscopy (SEM and TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). The microtubes have an entire hollow interior, open ends with rectangular cross-section, a large interior of 1.4-1.8μm width, and the thin walls of 80-100 nm. The obtained products exhibit excellent crystalline nature, high chemical and thermo-dynamic stability, excellent biocompatibility, as well as innocuity. It is believed that these well-defined microtubular structures of an organic material will be used as active materials for solar cells, nanodevices for field emission apparatus, microchannels for biochip and microvessel for drug delivery.

  10. Dielectric Properties of Reduced Graphene Oxide/Copper Phthalocyanine Nanocomposites Fabricated Through π- π Interaction

    Science.gov (United States)

    Wang, Zicheng; Wei, Renbo; Liu, Xiaobo

    2017-01-01

    Reduced graphene oxide/copper phthalocyanine nanocomposites are successfully prepared through a simple and effective two-step method, involving preferential reduction of graphene oxide and followed by self-assembly with copper phthalocyanine. The results of photographs, ultraviolet visible, x-ray diffraction, x-ray photoelectron spectroscopy, and scanning electron microscopy show that the in situ blending method can effectively facilitate graphene sheets to disperse homogenously in the copper phthalocyanine matrix through π- π interactions. As a result, the reduction of graphene oxide and restoration of the sp 2 carbon sites in graphene can enhance the dielectric properties and alternating current conductivity of copper phthalocyanine effectively.

  11. Water-soluble copper phthalocyanine for optimization of gas-sensor characteristics of tin dioxide upon adsorption of ammonia

    Science.gov (United States)

    Komolov, A. S.; Lazneva, E. F.; Gerasimova, N. B.; Zimina, M. V.; Si, P.; Panina, Yu. A.

    2015-12-01

    This paper presents the results of the investigation into the electrical conductivity of thin films based on tin dioxide (SnO2) nanoparticles, a film consisting of copper phthalocyanine-3,4',4″,4‴-tetrasulfonic acid tetrasodium salt (CuPc-4SO3Na) molecules, and a composite film based on a mixture of equal parts by volume of the two materials upon adsorption of ammonia. The adsorption experiments have been carried out in a vacuum at room temperature with an increase in the ammonia pressure to 3 × 103 Pa from the residual gas base pressure of 5 × 10-1 Pa. It has been found that, in the case of a single-component film based on SnO2 nanoparticles, an increase in the electrical conductivity reaches 100% and is not completely reversible at room temperature after evacuation of the gas. For the single-component CuPc-4SO3Na film and the composite CuPc-4SO3Na/SnO2 film, the electrical conductivities increase by a factor of 400 and 150, respectively. Upon evacuation of ammonia to the base pressure, the electrical conductivity decreases to the initial values for 1 s. The mechanism of the influence of adsorbed ammonia molecules on the electrical conductivity of the composite material under investigation has been discussed using the model of the formation of the composite sample, according to which the organic component is located in voids between the SnO2 nanoparticles.

  12. Effect of thickness and temperature of copper phthalocyanine films on their properties

    Directory of Open Access Journals (Sweden)

    Alieva Kh. S.

    2012-06-01

    Full Text Available The research has shown that copper phthalocyanine films, having a set of unique properties, can be successfully used as gas-sensitive coating of resistive structures. The thickness of the film, in contrast to its temperature, is not the determining factor for high sensitivity. Low operating temperature of structures with copper phthalocyanine films allows to exploit them in economy mode.

  13. Trap States in Copper Phthalocyanine Thin Films using Photogenerated Currents

    Science.gov (United States)

    Gredig, Thomas; Guerra, Jorge; Byrne, Matthew; Silverstein, Evan

    2010-03-01

    The efficiency of organic solar cells is limited by several factors including the photocurrent generation process. Copper phthalocyanine thin films with different grain structures are prepared via thermal evaporation onto interdigitated gold electrodes. The samples are analyzed with atomic force microscopy and then exposed to light pulses to explore the time dependence of photogenerated currents in phthalocyanine thin films. The average grain size is obtained from the correlation length of the height-height correlation function and varies from 30-200nm. The dependence of the recombination of photo-excited, dissociated charge pairs on the electric field is compared with the Onsager mechanism and a simple dual trap state model from which relevant time scales are extracted.

  14. AC impedance spectroscopy on copper phthalocyanine thin films

    Science.gov (United States)

    Robinson, Kyle P.

    Impedance spectroscopy is used to study copper phthalocyanine thin films in order to disentangle the contributions of the crystal and the unavoidable grain boundaries. The spectroscopy data is fit with an equivalent circuit model to determine resistance, capacitance, and activation energy for different grain morphologies. The copper phthalocyanine thin films are deposited via thermal evaporation on platinum interdigitated electrodes on glass substrates at different temperatures from 300 to 530 K with constant thickness of 22 nm. AC measurements, implementing a precision LCR meter are taken from 20Hz - 2 MHz, and at measurement temperatures from 25 - 90 °C. Stabilizing current by subjecting samples to 5 days in the dark, the impedance spectrum can be represented by Cole-Cole plots, which show either one or two peaks. The two maxima may be attributed to the crystalline bulk and grain boundaries of the film. We observe that the grain boundary resistance component changes by three orders of magnitude when varying the grain morphology, and the capacitance changes by one order of magnitude. The resistance of the grain boundary shows a minimum near the phase transition temperature of 450 K, followed by an increase in resistance for samples deposited at higher temperatures. The capacitance on the other hand, shows a maximum near the phase transition temperature. Similarly, the activation energy for the grain boundary peaks at 1.29 +/- 0.12 eV at the same phase-transition tempemture, whereas the crystalline bulk component has a constant activation energy of 0.36 +/- 0.08 eV for all sample of different grain sizes. Additional data taken using a perpendicular configuration for a 30 nm thick cobalt phthalocyanine thin film shows a double peak. The low temperature measurements for these samples are interpreted to have two contributions from micro-shorts and crystalline bulk.

  15. Copper phthalocyanine-based CMPs with various internal structures and functionalities.

    Science.gov (United States)

    Ding, Xuesong; Han, Bao-Hang

    2015-08-18

    Several kinds of copper phthalocyanine-based conjugated microporous polymers have been synthesized, which present enhanced long-wavelength photon absorption capability and high efficiency for singlet oxygen generation under low energy light irradiation. This strategy opens a facile avenue towards expanding the scope of phthalocyanine-based porous materials with various internal structures and functionalities.

  16. Copper phthalocyanine films deposited by liquid-liquid interface recrystallization technique (LLIRCT).

    Science.gov (United States)

    Patil, K R; Sathaye, S D; Hawaldar, R; Sathe, B R; Mandale, A B; Mitra, A

    2007-11-15

    The simple recrystallization process is innovatively used to obtain the nanoparticles of copper phthalocyanine by a simple method. Liquid-liquid interface recrystallization technique (LLIRCT) has been employed successfully to produce small sized copper phthalocyanine nanoparticles with diameter between 3-5 nm. The TEM-SAED studies revealed the formation of 3-5 nm sized with beta-phase dominated mixture of alpha and beta copper phthalocyanine nanoparticles. The XRD, SEM, and the UV-vis studies were further carried out to confirm the formation of copper phthalocyanine thin films. The cyclic voltametry (CV) studies conclude that redox reaction is totally reversible one electron transfer process. The process is attributed to Cu(II)/Cu(I) redox reaction.

  17. Spin Exchange Interaction in Substituted Copper Phthalocyanine Crystalline Thin Films

    Science.gov (United States)

    Rawat, Naveen; Pan, Zhenwen; Lamarche, Cody J.; Wetherby, Anthony; Waterman, Rory; Tokumoto, Takahisa; Cherian, Judy G.; Headrick, Randall L.; McGill, Stephen A.; Furis, Madalina I.

    2015-11-01

    The origins of spin exchange in crystalline thin films of Copper Octabutoxy Phthalocyanine (Cu-OBPc) are investigated using Magnetic Circular Dichroism (MCD) spectroscopy. These studies are made possible by a solution deposition technique which produces highly ordered films with macroscopic grain sizes suitable for optical studies. For temperatures lower than 2 K, the contribution of a specific state in the valence band manifold originating from the hybridized lone pair in nitrogen orbitals of the Phthalocyanine ring, bears the Brillouin-like signature of an exchange interaction with the localized d-shell Cu spins. A comprehensive MCD spectral analysis coupled with a molecular field model of a σπ - d exchange analogous to sp-d interactions in Diluted Magnetic Semiconductors (DMS) renders an enhanced Zeeman splitting and a modified g-factor of -4 for the electrons that mediate the interaction. These studies define an experimental tool for identifying electronic states involved in spin-dependent exchange interactions in organic materials.

  18. Dispersion of Metal Phthalocyanines on Surface of TiO2

    Institute of Scientific and Technical Information of China (English)

    ZHU Jian-Feng; WANG Chun-Ming; ZHU Yue-Xiang; ZHAO Bi-Ying; XIE You-Chang

    2005-01-01

    Dispersion of copper(Ⅱ) phthalocyanine (CuPc), copper(Ⅱ) phthalocyaninesulfonate (CuPcS) and cobalt(Ⅱ)phthalocyaninetetrasulfonate (CoPcTS) on the surface of titanium dioxide was investigated by XRD, XPS, FT-IR and UV-Vis techniques. Results show that interaction between CuPc and TiO2 was very weak and CuPc was difficult to disperse on the surface of the support. While partly sulfurized CuPcS could be dispersed on the surface of support through sulfo-groups and its dispersion capacity was determined to be 0.085 g CuPcS/g TiO2. Completely sulfurized CoPcTS could also be dispersed on the surface of TiO2 as a monolayer and its dispersion capacity was 0.12 g CoPcTS/g TiO2. Interactions of the sulfo-groups as well as the electrons of CoPcTS with the surface of TiO2could be evidenced by FT-IR characterization. Therefore, it was suggested that CoPcTS molecules be adsorbed on the surface of TiO2 in a flat-lying mode while CuPcS in a slanting one. UV-Vis spectra show that the dispersed CuPcS and CoPcTS molecules exist in both forms of monomers and dimers.

  19. Identification of copper phthalocyanine blue polymorphs in unaged and aged paint systems by means of micro-Raman spectroscopy and Random Forest.

    Science.gov (United States)

    Anghelone, Marta; Jembrih-Simbürger, Dubravka; Schreiner, Manfred

    2015-10-05

    Copper phthalocyanine (CuPc) blues (PB15) are largely used in art and industry as pigments. In these fields mainly three different polymorphic modifications of PB15 are employed: alpha, beta and epsilon. Differentiating among these CuPc forms can give important information for developing conservation strategy and can help in relative dating, since each form was introduced in the market in different time periods. This study focuses on the classification of Raman spectra measured using 532 nm excitation wavelength on: (i) dry pigment powders, (ii) unaged mock-ups of self-made paints, (iii) unaged commercial paints, and (iv) paints subjected to accelerated UV ageing. The ratios among integrated Raman bands are taken in consideration as features to perform Random Forest (RF). Features selection based on Gini Contrast score was carried out on the measured dataset to determine the Raman bands ratios with higher predictive power. These were used as polymorphic markers, in order to establish an easy and accessible method for the identification. Three different ratios and the presence of a characteristic vibrational band allowed the identification of the crystal modification in pigments powder as well as in unaged and aged paint films.

  20. Sensing of volatile organic compounds by copper phthalocyanine thin films

    Science.gov (United States)

    Ridhi, R.; Saini, G. S. S.; Tripathi, S. K.

    2017-02-01

    Thin films of copper phthalocyanine have been deposited by thermal evaporation technique. We have subsequently exposed these films to the vapours of methanol, ethanol and propanol. Optical absorption, infrared spectra and electrical conductivities of these films before and after exposure to chemical vapours have been recorded in order to study their sensing mechanisms towards organic vapours. These films exhibit maximum sensing response to methanol while low sensitivities of the films towards ethanol and propanol have been observed. The changes in sensitivities have been correlated with presence of carbon groups in the chemical vapours. The effect of different types of electrodes on response-recovery times of the thin film with organic vapours has been studied and compared. The electrodes gap distance affects the sensitivity as well as response-recovery time values of the thin films.

  1. Adsorption study of copper phthalocyanine on Si(111)(√3 × √3)R30°Ag surface

    Science.gov (United States)

    Menzli, S.; Ben Hamada, B.; Arbi, I.; Souissi, A.; Laribi, A.; Akremi, A.; Chefi, C.

    2016-04-01

    The adsorption of copper phthalocyanine (CuPc) molecules on Si(111)(√3 × √3)R30°Ag surface is studied at room temperature under ultra high vacuum. Crystallographic, chemical and electronic properties of the interface are investigated by low energy electron diffraction (LEED), ultraviolet and X-ray photoemission spectroscopies (UPS, XPS) and X-ray photoemission diffraction (XPD). LEED and XPD results indicate that after one monolayer deposition the molecular layer is highly ordered with a flat lying adsorption configuration. The corresponding pattern reveals the coexistence of three symmetrically equivalent orientations of molecules with respect to the substrate. XPS core level spectra of the substrate reveal that there is no discernible chemical interaction between molecules and substrate; however there is evidence of Fermi level movement. During the growth, the work function was found to decrease from 4.90 eV for the clean substrate to 4.35 eV for the highest coverage (60 monolayers). Within a thickness of two monolayer deposition an interface dipole of 0.35 eV and a band bending of 0.2 eV have been found. UPS spectra indicate the existence of a band bending of the highest occupied molecular orbital (HOMO) of 0.55 eV. The changes in the work function, in the Fermi level position and in the HOMO state have been used to determine the energy level alignment at the interface.

  2. Controlled assembly of copper phthalocyanine with 1-iodooctadecane

    Institute of Scientific and Technical Information of China (English)

    LEI Shengbin; WANG Chen; WAN Lijun; BAI Chunli

    2003-01-01

    The binary assembly behavior of 1-iodoocta- decane with substituted phthalocyanine (Pc) is studied using the scanning tunneling microscopy (STM). By altering the substituted alkyl groups attached to the phthalocyanine ring, either uniform assembly or phase separation behavior can be observed. It is suggested that the strength of intermolecular interaction between phthalocyanine molecules is the determining factor for the assembly structure.

  3. Structural templating in a nonplanar phthalocyanine using single crystal copper iodide

    OpenAIRE

    Rochford, L. A. (Luke A.); Ramadan, Alexandra J.; Keeble, Dean S.; Ryan, Mary P.; Heutz, Sandrine; Jones, T S

    2015-01-01

    Solution-grown copper iodide crystals are used as substrates for the templated growth of the nonplanar vanadyl phthalocyanine using organic molecular beam deposition. Structural characterization reveals a single molecular orientation produced by the (111) Miller plane of the copper iodide crystals. These fundamental measurements show the importance of morphology and structure in templating interactions for organic electronics applications.

  4. Decolorization Treatment of Copper Phthalocyanine Textile Dye Wastewater by Electrochemical Methods

    Directory of Open Access Journals (Sweden)

    K. Dermentzis

    2013-01-01

    Full Text Available Electrochemical decolorization and degradation treatment of aqueous copper phthalocyanine reactive dye solutions was comparatively studied by electrocoagulation, electrooxidation and electro-Fenton processes. In the electrocoagulation process with aluminum electrodes the colored aqueous solutions of initial pH 6.4 containing 50 mg L-1 copper phthalocyanine and 6 g L-1 NaCl were treated at applied current densities of 2.5 and 5 mA cm-2. Fast and 100% decolorization was achieved in 4 and 2 minutes of electroprocessing respectively. The indirect electrooxidation process was conducted in acidic electrolyte solutions containing 50 mg L-1 copper phthalocyanine and 6 g L-1 NaCl with Ti/Pt and graphite plate electrodes at the applied current density of 10 mA cm-2. Even after 90 minutes of electrolysis time the dye remained by 23 and 18.8 % respectively undegradable. By the direct and indirect electrooxidation with the same amount of Na2SO4 electrolyte and added H2O2 respectively and using the same electrodes, the copper phthalocyanine dye was not or was only barely degraded respectively. In the electro-Fenton process with Fe electrodes and added amounts of H2O2 at pH 3 and an applied current density of 5 mA/cm2 complete degradation of copper phthalocyanine occurred in 15 minutes.

  5. Effect of CuPc layer insertion on the memory performance of CdS nanocomposite diodes

    Energy Technology Data Exchange (ETDEWEB)

    Tripathi, S.K., E-mail: surya@pu.ac.in; Kaur, Ramneek; Jyoti

    2016-09-15

    Highlights: • CdS nanocomposite as an active layer investigated for memory device application. • Effect of copper phthalocyanine layer insertion on the memory performance studied. • Bipolar switching behaviour with high ON/OFF ratio ∼1.4 × 10{sup 4}. • Series resistance and interface states dominate the electrical properties of the device. - Abstract: In the present work, semiconductor diodes with CdS nanocomposite as an active layer have been fabricated and investigated for memory device applications. The effect of copper phthalocyanine (CuPc) layer insertion between the bottom electrode and CdS nanocomposite has been studied. I–V characteristics show electrical hysteresis behaviour vital for memory storage application. The as-fabricated devices exhibit bipolar switching behaviour with OFF to ON state transition at positive bias and vice versa. Device with CuPc layer exhibits I{sub ON}/I{sub OFF} ratio ∼ 1.4 × 10{sup 4}. Possible conduction mechanism has been described on the basis of theoretical current conduction models. The frequency dispersion capacitance, series resistance and conductance of the devices have been studied and discussed. At low frequency, the series resistance and the interface states dominate the electrical properties of the device. The results indicate that the multilayered devices open up the possibility of new generation non-volatile memory devices with low cost, high density and stability.

  6. Electronic properties and orbital-filling mechanism in Rb-intercalated copper phthalocyanine

    NARCIS (Netherlands)

    Evangelista, F.; Gotter, R.; Mahne, N.; Nannarone, S.; Ruocco, A.; Rudolf, P.

    2008-01-01

    The evolution of the electronic properties of a thin film of copper phthalocyanine deposited on Al(100) and progressively intercalated with rubidium atoms was followed by photoemission and X-ray absorption spectroscopies. Electron donation from the Rb atoms to the C32H16N8Cu molecules results in the

  7. Electronic properties and orbital-filling mechanism in Rb-intercalated copper phthalocyanine

    NARCIS (Netherlands)

    Evangelista, F.; Gotter, R.; Mahne, N.; Nannarone, S.; Ruocco, A.; Rudolf, P.

    2008-01-01

    The evolution of the electronic properties of a thin film of copper phthalocyanine deposited on Al(100) and progressively intercalated with rubidium atoms was followed by photoemission and X-ray absorption spectroscopies. Electron donation from the Rb atoms to the C32H16N8Cu molecules results in the

  8. Optical modeling of organic solar cells based on CuPc and C60.

    Science.gov (United States)

    Monestier, Florent; Simon, Jean-Jacques; Torchio, Philippe; Escoubas, Ludovic; Ratier, Bernard; Hojeij, Wassim; Lucas, Bruno; Moliton, André; Cathelinaud, Michel; Defranoux, Christophe; Flory, François

    2008-05-01

    We have investigated the influence of the poly(3,4-ethylenedioxythiophene)-blend-poly(styrene-sulfonate) (PEDOT:PSS) layer on the short-circuit current density (J(sc)) of single planar heterojunction organic solar cells based on a copper phthalocyanine (CuPc)-buckminsterfullerene (C(60)) active layer. Complete optical and electrical modeling of the cell has been performed taking into account optical interferences and exciton diffusion. Comparison of experimental and simulated external quantum efficiency has allowed us to estimate the exciton diffusion length to be 37 nm for the CuPc and 19 nm for the C(60). The dependence of short-circuit current densities versus the thickness of the PEDOT:PSS layer is analyzed and compared with experimental data. It is found that the variation in short-circuit current densities could be explained by optical interferences.

  9. Interfacial Engineering of Perovskite Solar Cells by Employing a Hydrophobic Copper Phthalocyanine Derivative as Hole-Transporting Material with Improved Performance and Stability.

    Science.gov (United States)

    Jiang, Xiaoqing; Yu, Ze; Lai, Jianbo; Zhang, Yuchen; Hu, Maowei; Lei, Ning; Wang, Dongping; Yang, Xichuan; Sun, Licheng

    2017-04-22

    In high-performance perovskite solar cells (PSCs), hole-transporting materials (HTMs) play an important role in extracting and transporting the photo-generated holes from the perovskite absorber to the cathode, thus reducing unwanted recombination losses and enhancing the photovoltaic performance. Herein, solution-processable tetra-4-(bis(4-tert-butylphenyl)amino)phenoxy-substituted copper phthalocyanine (CuPc-OTPAtBu) was synthesized and explored as a HTM in PSCs. The optical, electrochemical, and thermal properties were fully characterized for this organic metal complex. The photovoltaic performance of PSCs employing this CuPc derivative as a HTM was further investigated, in combination with a mixed-ion perovskite as a light absorber and a low-cost vacuum-free carbon as cathode. The optimized devices [doped with 6 % (w/w) tetrafluoro-tetracyano-quinodimethane (F4TCNQ)] showed a decent power conversion efficiency of 15.0 %, with an open-circuit voltage of 1.01 V, a short-circuit current density of 21.9 mA cm(-2) , and a fill factor of 0.68. Notably, the PSC devices studied also exhibited excellent long-term durability under ambient condition for 720 h, mainly owing to the introduction of the hydrophobic HTM interlayer, which prevents moisture penetration into the perovskite film. The present work emphasizes that solution-processable CuPc holds a great promise as a class of alternative HTMs that can be further explored for efficient and stable PSCs in the future. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Dry Etching of Copper Phthalocyanine Thin Films: Effects on Morphology and Surface Stoichiometry

    OpenAIRE

    Brett, Michael J.; Dijken, Jaron G. Van

    2012-01-01

    We investigate the evolution of copper phthalocyanine thin films as they are etched with argon plasma. Significant morphological changes occur as a result of the ion bombardment; a planar surface quickly becomes an array of nanopillars which are less than 20 nm in diameter. The changes in morphology are independent of plasma power, which controls the etch rate only. Analysis by X-ray photoelectron spectroscopy shows that surface concentrations of copper and oxygen increase with etch time, whi...

  11. Theoretical Scanning Tunnelling Microscopy Images of Metal (Fe, Co, Ni and Cu) Phthalocyanines

    Institute of Scientific and Technical Information of China (English)

    李群祥; 朱清时; 袁岚峰; 杨金龙; 侯建国

    2001-01-01

    The scanning tunnelling microscopy (STM) images of isolated iron phthalocyanine (FePc), cobalt phthalocyanine (CoPc), nickel phthalocyanine (NiPc) and copper phthalocyanine (CuPc) are simulated theoretically. All the simulated STM images show submolecular structures and reproduce well the features of the experimental images. The results show that there is a strong dependence of the STM images on the ion valence configuration of the metal ion. At the small tip bias voltages of less than 0.5 V, the central metal ions in NiPc and CuPc appear as holes in the molecular images, while they are the highlighted bumps in FePc and CoPc. The simulated images are interpreted by the fact that both FePc and CoPc systems have a significant dz2 character near the Fermi level while the NiPc and CuPc systems do not. Moreover, we predict that the central nickel ion for NiPc appears as a highlighted point when the tip bias voltage is larger than 0.7 V.

  12. Electrochemical and optical characterization of cobalt, copper and zinc phthalocyanine complexes.

    Science.gov (United States)

    Lee, Jaehyun; Kim, Se Hun; Lee, Woosung; Lee, Jiwon; An, Byeong-Kwan; Oh, Se Young; Kim, Jae Pil; Park, Jongwook

    2013-06-01

    New phthalocyanine (Pc) derivatives that include the alkyl group in ligand were synthesized based on three core metals such as zinc (Zn), copper (Cu), and cobalt (Co). Electrochemical behaviors and optical properties of the new phthalocyanine derivatives with ligand and different core metal were investigated by using cyclic voltammetry, UV-Visible (UV-Vis) spectroscopy and photoluminescence (PL) spectroscopy. In UV-Vis data, maximum values of 2H, Co, Cu, and Zn complexes were 708 nm and 677 nm, 686 nm, 684 nm, respectively.

  13. SEMICONDUCTOR DEVICES: Impedance hygrometer based on cellulose and CuPc

    Science.gov (United States)

    Karimov, Kh. S.; Qasuria, T. A.; Ahmad, Zubair

    2010-06-01

    An investigation has been made on the properties of an impedance hygrometer fabricated using cellulose and copper phthalocyanine (Ag/cellulose/CuPc/Ag). A 5wt% suspension of cellulose was prepared in water while the CuPc was dissolved in methanol. Cellulose film was deposited on glass substrates with preliminary deposited metallic electrodes followed by deposition of CuPc film. The resistances and capacitances of the samples were evaluated under the effect of humidity. The impedance was calculated from resistance and capacitance measurements. It was also measured during the experiment. It was observed that the capacitance of the sensor increases and resistance and impedance decrease with an increase in the relative humidity level. It was found that the impedance-humidity relationship showed more uniform changes in the interval of 31%-98% RH than the resistance- and capacitance-humidity relationships that showed visible changes in the humidity intervals of 31%-80% RH and 80%-98% RH respectively. The humidity-dependent impedance of the sample makes it attractive for use in impedance hygrometers. The impedance hygrometer may be used in instruments for the environmental monitoring of humidity.

  14. Dry Etching of Copper Phthalocyanine Thin Films: Effects on Morphology and Surface Stoichiometry

    Directory of Open Access Journals (Sweden)

    Michael J. Brett

    2012-08-01

    Full Text Available We investigate the evolution of copper phthalocyanine thin films as they are etched with argon plasma. Significant morphological changes occur as a result of the ion bombardment; a planar surface quickly becomes an array of nanopillars which are less than 20 nm in diameter. The changes in morphology are independent of plasma power, which controls the etch rate only. Analysis by X-ray photoelectron spectroscopy shows that surface concentrations of copper and oxygen increase with etch time, while carbon and nitrogen are depleted. Despite these changes in surface stoichiometry, we observe no effect on the work function. The absorbance and X-ray diffraction spectra show no changes other than the peaks diminishing with etch time. These findings have important implications for organic photovoltaic devices which seek nanopillar thin films of metal phthalocyanine materials as an optimal structure.

  15. Dry etching of copper phthalocyanine thin films: effects on morphology and surface stoichiometry.

    Science.gov (United States)

    Van Dijken, Jaron G; Brett, Michael J

    2012-08-24

    We investigate the evolution of copper phthalocyanine thin films as they are etched with argon plasma. Significant morphological changes occur as a result of the ion bombardment; a planar surface quickly becomes an array of nanopillars which are less than 20 nm in diameter. The changes in morphology are independent of plasma power, which controls the etch rate only. Analysis by X-ray photoelectron spectroscopy shows that surface concentrations of copper and oxygen increase with etch time, while carbon and nitrogen are depleted. Despite these changes in surface stoichiometry, we observe no effect on the work function. The absorbance and X-ray diffraction spectra show no changes other than the peaks diminishing with etch time. These findings have important implications for organic photovoltaic devices which seek nanopillar thin films of metal phthalocyanine materials as an optimal structure.

  16. Effect of external electric field on morphology of copper phthalocyanine-fullerene blended films during annealing

    Science.gov (United States)

    Parhi, Anukul Prasad; Iyer, S. Sundar Kumar

    2016-03-01

    The thin-film morphology and segregated phases of constituents in blends of organic semiconductors play an important role in determining the performance of devices fabricated with these constituents. In this study, we explored the effect of an external electric field applied during annealing on the morphology and phase of blended films of two popular organic semiconductors, copper pthalocyanine (CuPc) and buckminsterfullerene (C60). Films of different blend ratios annealed at various temperatures in both the presence and absence of an electric field were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and ultraviolet-visible (UV-vis) spectroscopy. The characteristics of annealed pristine CuPc films were also included for comparison. The observed changes in the properties of the blended films following the annealing, including the abrupt phase segregation of the blended constituents in the films, are discussed. The polarizability of the molecules was calculated using density functional theory (DFT) to explain the interaction, stacking, and segregation of the molecules in the blend. The results showed that application of an electric field during annealing of the blended films is an additional control parameter that can help tune the properties of the blended film. [Figure not available: see fulltext.

  17. Conducting Polymers Functionalized with Phthalocyanine as Nitrogen Dioxide Sensors

    Directory of Open Access Journals (Sweden)

    S. D. Deshpande

    2002-05-01

    Full Text Available The conducting polymers such as polyaniline, polypyrrole and polythiophene were functionalized with copper phthalocyanine using chemical oxidation method. The obtained polymers viz. PANI-CuPc, PPy-CuPc and PT-CuPc were studied as chemical sensors by their response characteristics after exposure to various chemical vapors such as methanol, ammonia and nitrogen dioxide. The results obtained showed that these polymers have moderate sensitivity towards the methanol as well as ammonia vapors whereas they show tremendous sensitivity towards nitrogen dioxide vapors. The sensitivity factor of as high as 50,000 was obtained for PT-CuPc polymers in nitrogen dioxide. In comparison to this, the sensitivity factors of about 100 and 40 were obtained, when these polymers were exposed to ammonia and methanol vapors. The very high selectivity towards the nitrogen dioxide was explained on the basis of charge transfer complex formed between, the phthalocyanine donor and nitrogen dioxide acceptor molecules. On the other hand, ammonia becomes a competing electron donor in CuPc containing conducting polymers. The very low response towards the methanol may be explained on the basis very little charge transfer / interaction between CuPc containing polymers and methanol. Thus, CuPc incorporated conducting polymers have much higher selectivity than their original homopolymer.

  18. Ordering of Zn-centered porphyrin and phthalocyanine on TiO2(011: STM studies

    Directory of Open Access Journals (Sweden)

    Piotr Olszowski

    2017-01-01

    Full Text Available Zn(IIphthalocyanine molecules (ZnPc were thermally deposited on a rutile TiO2(011 surface and on Zn(IImeso-tetraphenylporphyrin (ZnTPP wetting layers at room temperature and after elevated temperature thermal processing. The molecular homo- and heterostructures were characterized by high-resolution scanning tunneling microscopy (STM at room temperature and their geometrical arrangement and degree of ordering are compared with the previously studied copper phthalocyanine (CuPc and ZnTPP heterostructures. It was found that the central metal atom may play some role in ordering and growth of phthalocyanine/ZnTPP heterostructures, causing differences in stability of upright standing ZnPc versus CuPc molecular chains at given thermal annealing conditions.

  19. Temperature-assisted morphological transition in CuPc thin films

    Science.gov (United States)

    Bae, Yu Jeong; Pham, Thi Kim Hang; Kim, Tae Hee

    2016-05-01

    Ex-situ and in-situ morphological analyses were performed for Cu-phthalocyanine (CuPc) organic semiconductor films by using atomic force microscopy (AFM) and reflection high-energy electron diffraction (RHEED). The focus was the effects of post-annealing on the structural characteristics of CuPc films grown on MgO(001) layers by using an ultra-high-vacuum thermal evaporator. Sphere-to-nanofibril and 2-D to 3-D morphological transitions were observed with increasing CuPc thickness beyond 3 nm. The surface morphology and the crystallinity were drastically improved after an additional cooling of the post-annealed CuPc films thinner than 3 nm. Our results highlight that molecular orientation and structural ordering can be effectively controlled by using different temperature treatments and a proper combination of material, film thickness, and substrate.

  20. Tetra-methyl substituted copper (II phthalocyanine as a hole injection enhancer in organic light-emitting diodes

    Directory of Open Access Journals (Sweden)

    Yu-Long Wang

    2015-10-01

    Full Text Available We have enhanced hole injection and lifetime in organic light-emitting diodes (OLEDs by incorporating the isomeric metal phthalocyanine, CuMePc, as a hole injection enhancer. The OLED devices containing CuMePc as a hole injection layer (HIL exhibited higher luminous efficiency and operational lifetime than those using a CuPc layer and without a HIL. The effect of CuMePc thickness on device performance was investigated. Atomic force microscope (AFM studies revealed that the thin films were smooth and uniform because the mixture of CuMePc isomers depressed crystallization within the layer. This may have caused the observed enhanced hole injection, indicating that CuMePc is a promising HIL material for highly efficient OLEDs.

  1. Tetra-methyl substituted copper (II) phthalocyanine as a hole injection enhancer in organic light-emitting diodes

    Science.gov (United States)

    Wang, Yu-Long; Xu, Jia-Ju; Lin, Yi-Wei; Chen, Qian; Shan, Hai-Quan; Yan, Yan; Roy, V. A. L.; Xu, Zong-Xiang

    2015-10-01

    We have enhanced hole injection and lifetime in organic light-emitting diodes (OLEDs) by incorporating the isomeric metal phthalocyanine, CuMePc, as a hole injection enhancer. The OLED devices containing CuMePc as a hole injection layer (HIL) exhibited higher luminous efficiency and operational lifetime than those using a CuPc layer and without a HIL. The effect of CuMePc thickness on device performance was investigated. Atomic force microscope (AFM) studies revealed that the thin films were smooth and uniform because the mixture of CuMePc isomers depressed crystallization within the layer. This may have caused the observed enhanced hole injection, indicating that CuMePc is a promising HIL material for highly efficient OLEDs.

  2. Tetra-methyl substituted copper (II) phthalocyanine as a hole injection enhancer in organic light-emitting diodes

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yu-Long; Xu, Jia-Ju; Lin, Yi-Wei; Chen, Qian; Shan, Hai-Quan; Xu, Zong-Xiang, E-mail: xu.zx@sustc.edu.cn, E-mail: val.roy@cityu.edu.hk [Department of Chemistry, South University of Science and Technology of China, Shenzhen, Guangdong, P. R. China, 518055 (China); Yan, Yan; Roy, V. A. L., E-mail: xu.zx@sustc.edu.cn, E-mail: val.roy@cityu.edu.hk [Department of Physics and Materials Science, City University of Hong Kong, Hong Kong SAR (Hong Kong)

    2015-10-15

    We have enhanced hole injection and lifetime in organic light-emitting diodes (OLEDs) by incorporating the isomeric metal phthalocyanine, CuMePc, as a hole injection enhancer. The OLED devices containing CuMePc as a hole injection layer (HIL) exhibited higher luminous efficiency and operational lifetime than those using a CuPc layer and without a HIL. The effect of CuMePc thickness on device performance was investigated. Atomic force microscope (AFM) studies revealed that the thin films were smooth and uniform because the mixture of CuMePc isomers depressed crystallization within the layer. This may have caused the observed enhanced hole injection, indicating that CuMePc is a promising HIL material for highly efficient OLEDs.

  3. Fluorinated copper phthalocyanine nanowires for enhancing interfacial electron transport in organic solar cells.

    Science.gov (United States)

    Yoon, Seok Min; Lou, Sylvia J; Loser, Stephen; Smith, Jeremy; Chen, Lin X; Facchetti, Antonio; Marks, Tobin J; Marks, Tobin

    2012-12-12

    Zinc oxide is a promising candidate as an interfacial layer (IFL) in inverted organic photovoltaic (OPV) cells due to the n-type semiconducting properties as well as chemical and environmental stability. Such ZnO layers collect electrons at the transparent electrode, typically indium tin oxide (ITO). However, the significant resistivity of ZnO IFLs and an energetic mismatch between the ZnO and the ITO layers hinder optimum charge collection. Here we report that inserting nanoscopic copper hexadecafluorophthalocyanine (F(16)CuPc) layers, as thin films or nanowires, between the ITO anode and the ZnO IFL increases OPV performance by enhancing interfacial electron transport. In inverted P3HT:PC(61)BM cells, insertion of F(16)CuPc nanowires increases the short circuit current density (J(sc)) versus cells with only ZnO layers, yielding an enhanced power conversion efficiency (PCE) of ∼3.6% vs ∼3.0% for a control without the nanowire layer. Similar effects are observed for inverted PTB7:PC(71)BM cells where the PCE is increased from 8.1% to 8.6%. X-ray scattering, optical, and electrical measurements indicate that the performance enhancement is ascribable to both favorable alignment of the nanowire π-π stacking axes parallel to the photocurrent flow and to the increased interfacial layer-active layer contact area. These findings identify a promising strategy to enhance inverted OPV performance by inserting anisotropic nanostructures with π-π stacking aligned in the photocurrent flow direction.

  4. Synthesis and aggregation study of optically active tetra--[()-2-octanyloxy]-substituted copper and nickel phthalocyanines

    Indian Academy of Sciences (India)

    Fang-Di Cong; Gui Gao; Jian-Xin Li; Guo-Qing Huang; Zhen Wei; Feng-Yang Yu; Xi-Guang Du; Ke-Zhi Xing

    2010-11-01

    The optically active tetra--[()-2-octanyloxy]-substituted copper and nickel phthalocyanines were synthesized via a two-step route with 4-nitro-phthalonitrile and ()-2-octanol as the starting materials. Both compounds are fully characterized by MS, 1H NMR, UV-Vis, IR, CD and elemental analysis, and soluble in common organic solvents except methanol. The results showed that they were dispersed into single molecules in chloroform and dichloromethane, but prone to congregate into H-type aggregates in ethanol and diethyl ether. They assembled to H-type aggregates with left-handed helix when deposited as thin films.

  5. Chemistry and electronic properties of ferromagnetic metal-organic semiconductor interfaces: Fe on CuPc

    Energy Technology Data Exchange (ETDEWEB)

    Aristov, V.Yu. [IFW Dresden, 01069 Dresden (Germany); Institute of Solid State Physics, Russian Academy of Sciences, Chernogolovka, Moscow distr., 142432 (Russian Federation); Molodtsova, O.V.; Knupfer, M. [IFW Dresden, 01069 Dresden (Germany); Ossipyan, Yu.A. [Institute of Solid State Physics, Russian Academy of Sciences, Chernogolovka, Moscow distr., 142432 (Russian Federation); Doyle, B.P. [TASC-INFM Laboratory, Area Science Park - Basovizza, 34012 Trieste (Italy); Department of Physics, University of Johannesburg, PO Box 524, Auckland Park, 2006 (South Africa); Nannarone, S. [TASC-INFM Laboratory, Area Science Park - Basovizza, 34012 Trieste (Italy); Dipartimento di Ingegneria dei Materiali ed Amb., Universita di Modena e Reggio Emilia (Italy)

    2009-12-15

    The chemistry and electronic properties of the interfaces formed between the ferromagnetic metal (Fe) and the model organic semiconductor copper phthalocyanine are investigated in ultra-high vacuum conditions for the case of metal deposition onto the organic molecular thin film. The studies were performed by means of core-level and valence-band high-resolution photoemission electron spectroscopy (PES) as well as near-edge X-ray absorption fine structure using synchrotron radiation. Metal overlayer formation on the top of the organic semiconductor was observed without substantial penetration of deposited metal species into the organic film. At the thin interface layer the ferromagnetic metal shows strong chemical interaction with the nitrogen and carbon of the organic films. Moreover, our results infer that, as a consequence of Fe deposition onto CuPc, central copper atoms of the organic molecules at the interface are reduced from Cu(II) to Cu(I), while Fe atoms are oxidized and/or the ferromagnetic metal replaces this central Cu atom. Further optimization of such an interface is thus required to allow and/or facilitate the injection of spin-polarized carriers into organic semiconductors. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  6. Copper Phthalocyanine Thin Film Morphology Impact on Impedance Spectrum

    Science.gov (United States)

    Robinson, Kyle; Gredig, Thomas

    2012-11-01

    Copper phthlacyanine thin films play an important role as the active layer in gas sensors, organic solar cells, and organic field-effect transistors. The surface morphology of such thin films can be controlled via modification of thermal deposition parameters. Thin films were deposited onto platinum interdigitated electrodes for impedance measurements to study the effect of structure on charge transport. The average grain size increases and changes from α- and β-phase for samples deposited in the temperature range of 295-534 K. AC measurements in the temperature range of 295-385 K reveal relaxation peaks in the impedance spectra. From this spectrum, essential properties are retrieved, such as relaxation times and effective capacities, and correlated with the film morphology. Subject to both photo- and 5-day-dark current trials, photodecay rates are extracted via effective impedance circuit analysis using a phenomenological model that includes contributions from the grain boundary and the bulk part of the grain. Results indicate that the resistance contribution of low frequency relaxation peaks decrease while approaching the phase transition temperature, and vice versa for capacitance. We attribute the low-frequency peaks to grain boundaries, which are reduced in high temperature deposited samples. Hyper β-phase deposition temperatures show a sudden rise in resistance and lower capacitance due to increased roughness of samples.

  7. Solution-processed copper phthalocyanine–gold nanoparticle hybrid nanocomposite thin films

    Energy Technology Data Exchange (ETDEWEB)

    Khurana, Parul; Thatai, Sheenam [Chemistry Department, Banasthali University, Rajasthan (India); Chaure, Nandu B., E-mail: n.chaure@physics.unipune.ac.in [Department of Physics, University of Pune, Pune 411007 (India); Mahamuni, Shailaja [Department of Physics, University of Pune, Pune 411007 (India); Kulkarni, Sulabha, E-mail: s.kulkarni@iiserpunr.ac.in [Department of Physics, Indian Institute of Science Education and Research, Pune 411021 (India)

    2014-08-28

    Copper phthalocyanine (CuPc) thin film and gold nanoparticles (Au NPs) of size ∼ 20 nm were deposited on conducting indium tin oxide coated glass substrates. Thin films were ∼ 500 nm thick having crystalline nature determined by surface profilometer and X-ray diffraction technique. The concentration of Au NPs in the films was varied whereas the concentration of CuPc was constant. It was observed that surface morphology varied with Au NP concentration increase in the films accompanied by changes in the optical spectra over 300-1000 nm range and increase in the electrical conduction but no changes in the Fourier transform infra-red spectra. Such nanocomposite films would be useful in the fabrication of organic solar cells. - Highlights: • Optical and electrical properties of CuPc film are enhanced upon loading of Au NPs. • Upon loading of Au NPs in CuPc the surface morphology changes from sheets to fibers. • The systematic enhancement in current is observed by increasing Au NPs in CuPc film. • The XRD peak intensity of CuPc reduced with an increase in the concentration of Au NPs.

  8. Room temperature ppb level Cl2 sensing using sulphonated copper phthalocyanine films.

    Science.gov (United States)

    Kumar, Arvind; Singh, A; Debnath, A K; Samanta, S; Aswal, D K; Gupta, S K; Yakhmi, J V

    2010-09-15

    We present room temperature chemiresistive gas sensing characteristics of drop casted sulphonated copper phthalocyanine (CuTsPc) films. It has been demonstrated that these films are highly selective to Cl(2) and the sensitivity in the 5-2000 ppb range varies linearly between 65 and 625%. However, for concentrations >or=2000 ppb, the response becomes irreversible, which is found to be due to the chemical bond formation between Cl(2) and SO(3)Na group of CuTsPc films. The X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) data confirms the oxidation of SO(3)Na group by Cl(2) gas. Copyright (c) 2010 Elsevier B.V. All rights reserved.

  9. Possible utilization of acrylic paint and copper phthalocyanine pigment sludge for vermiculture.

    Science.gov (United States)

    Majumdar, Deepanjan; Buch, Vaidehi; Macwan, Praisy; Patel, Jignesh

    2010-05-01

    Sludge generated from water treatment plants in two different paint and pigment manufacturing industries, one manufacturing CPC Green (copper phthalocyanine green) and the other acrylic (pure and styrene) washable distempers, synthetic enamels, fillers and putties, were used for culturing earthworms (Eisenia foetida Savigny). The possibility of getting a quality vermicompost was also explored. The sludges were used pure and mixed with month-old cow dung at 1:1, 1:2, 1:3, 2:1 and 3:1 ratios (sludge:cow dung). In pure sludges and in the 3:1 ratio, earthworms did not survive. Earthworms had very low survival in CPC Green sludge and its mixtures while acrylic paint sludge was very efficient in supporting worm growth and worm castings were generated quickly. Both sludges were alkaline, non-saline, but had appreciable Ca, Al, Pb, Zn, and Mn. CPC Green had high Cu (12,900 mg kg(-1)) and acrylic paint sludge had high total Cr (155 mg kg(-1)). High Ca and Al in both came from water treatment chemicals (lime and alum), while CPC Green itself is a copper-based pigment. The sludges were suitable for land application with regard to their metal contents, except for Cu in CPC Green. CPC Green did not support proper growth of plants (green gram, Vigna radiata (L). R. Wilcz.), while acrylic paint sludge supported growth in pure form and mixtures with soil.

  10. Photoelectron spectroscopic studies of ultra-thin CuPc layers on a Si(111)-(√3 × √3)R30°-B surface

    Science.gov (United States)

    Menzli, S.; Laribi, A.; Mrezguia, H.; Arbi, I.; Akremi, A.; Chefi, C.; Chérioux, F.; Palmino, F.

    2016-12-01

    The adsorption of copper phthalocyanine (CuPc) molecules on Si(111)-(√3 × √3)R30°-B surface is investigated at room temperature under ultra-high vacuum. Crystallographic, chemical and electronic properties of the interface are investigated by low energy electron diffraction (LEED), ultraviolet and X-ray photoemission spectroscopies (UPS, XPS) and X-ray photoemission diffraction (XPD). LEED and XPD results shed light on the growth mechanism of CuPc on this substrate. At one monolayer coverage the growth mode was characterized by the formation of crystalline 3D nanoislands. The molecular packing deduced from this study appears very close to the one of the bulk CuPc α phase. The 3D islands are formed by molecules aligned in a standing manner. XPS core level spectra of the substrate reveal that there is no discernible chemical interaction between molecules and substrate. However there is charge transfer from molecules to the substrate. During the growth, the work function (WF) was found to decrease from 4.50 eV for the clean substrate to 3.70 eV for the highest coverage (30 monolayers). Within a thickness of two monolayers deposition, an interface dipole of 0.50 eV was found. A substrate band bending of 0.25 eV was deduced over all the range of exposure. UPS spectra indicate the existence of a band bending of the highest occupied molecular orbital (HOMO) of 0.30 eV. The changes in the work function, in the Fermi level position and in the onset of the molecular HOMO state have been used to determine the energy level alignment at the interface.

  11. Effects of spin–orbit coupling and many-body correlations in STM transport through copper phthalocyanine

    Directory of Open Access Journals (Sweden)

    Benjamin Siegert

    2015-12-01

    Full Text Available The interplay of exchange correlations and spin–orbit interaction (SOI on the many-body spectrum of a copper phtalocyanine (CuPc molecule and their signatures in transport are investigated. We first derive a minimal model Hamiltonian in a basis of frontier orbitals that is able to reproduce experimentally observed singlet–triplet splittings. In a second step SOI effects are included perturbatively. Major consequences of the SOI are the splitting of former degenerate levels and a magnetic anisotropy, which can be captured by an effective low-energy spin Hamiltonian. We show that scanning tunneling microscopy-based magnetoconductance measurements can yield clear signatures of both these SOI-induced effects.

  12. Molecular resolution friction microscopy of Cu phthalocyanine thin films on dolomite (104) in water.

    Science.gov (United States)

    Nita, Paweł; Pimentel, Carlos; Luo, Feng; Milián-Medina, Begoña; Gierschner, Johannes; Pina, Carlos M; Gnecco, Enrico

    2014-07-21

    The reliability of ultrathin organic layers as active components for molecular electronic devices depends ultimately on an accurate characterization of the layer morphology and ability to withstand mechanical stresses on the nanoscale. To this end, since the molecular layers need to be electrically decoupled using thick insulating substrates, the use of AFM becomes mandatory. Here, we show how friction force microscopy (FFM) in water allows us to identify the orientation of copper(ii)phthalocyanine (CuPc) molecules previously self-assembled on a dolomite (104) mineral surface in ultra-high vacuum. The molecular features observed in the friction images show that the CuPc molecules are stacked in parallel rows with no preferential orientation with respect to the dolomite lattice, while the stacking features resemble well the single CuPc crystal structure. This proves that the substrate induction is low and makes friction force microscopy in water a suitable alternative to more demanding dynamic AFM techniques in ultra-high vacuum.

  13. Photooxidation of Furfural with Phthalocyanine-sensitized TiO2 Particle Under Xenon Lamp

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Copper phthalocyanine was selected as the photosensitizer to sensitize TiO2 in this experiment with furfural as the target pollutant. The composite catalysts (TiO2/CuPC) obtained showed a great activity under a xenon lamp. By experiments, the optimal preparation conditions of the composite catalysts were set as follows: the CuPC loading mass fraction was 1.5% , the mass fraction of acetylacetone was 0. 3% , and the stirring time was 10 h. UV-Vis diffuse reflectance spectra, XRD, and BET were used to characterize the properties of the composite catalysts, which showed that after loading CuPC on TiO2, the composite catalyst retained the same crystal structure as pure TiO2 and the wavelength range of its absorption spectrum was broadened to 600-700 nm while its surface area was smaller than that of the pure TiO2. Under the optimal conditions, 20 mg/L furfural solution was degraded by nearly 90% and TOC by about 70%. When the catalyst was reused 6 times, the activity of the catalyst was still retained by about 75%.

  14. Molecular switching analyzed with sub-molecular precision: CuPc on Cu(111)

    Energy Technology Data Exchange (ETDEWEB)

    Schaffert, Johannes; Cottin, Maren; Sonntag, Andreas; Karacuban, Hatice; Bobisch, Christian; Moeller, Rolf [Faculty of Physics, Center for Nanointegration Duisburg-Essen, University of Duisburg-Essen, 47048 Duisburg (Germany); Lorente, Nicolas [Centro de Investigacion en Nanociencia y Nanotecnologia, Campus de la Universitat Autonoma de Barcelona, 08193 Bellaterra (Spain)

    2011-07-01

    The current fluctuations in Scanning Tunneling Microscopy and Spectroscopy have been analyzed in real time using special analogue electronics. This type of Scanning Action Microscopy technique allows to map topography and switching processes simultaneously. For the Cu-Phthalocyanine (CuPc) molecule on Cu(111), switching between two states is observed. The switching frequency, the switching amplitude and the ratio between the residence times in the observed states can be studied with Angstrom spacial resolution. Spectroscopic data obtained at 7 K yields information about the involved electronic states. Based on the experimental data as well as DFT calculations a model is presented. The CuPc molecule switches between different adsorption configurations, which are attributed to different angles of molecular rotation on the Cu(111) surface.

  15. Chemistry and electronic properties of metal-organic semiconductor interfaces: Fe and Co on CuPc

    Energy Technology Data Exchange (ETDEWEB)

    Aristov, Victor; Molodtsova, Olga; Knupfer, Martin [IFW Dresden, D-01069 Dresden (Germany); Ossipyan, Yurii [Institute of Solid State Physics,sian Academy of Sciences, Chernogolovka, Moscow (Russian Federation); Doyle, Bryan [TASC-INFM Laboratory, Trieste (Italy); Nannarone, Stefano [TASC-INFM Laboratory, Trieste (Italy); Dipartimento di Ingegneria dei Materiali ed Amb., Universita di Modena (Italy)

    2007-07-01

    The creation of a spin transistor based on a semiconductor was proposed in 1990 by Datta and Das. Nowadays the attractive idea to create a spin-transistor based on an organic semiconductor thin film (OMTF) has been proposed. The main problem in the development of such a device is to produce ferromagnetic metallic contacts as an injector of spin-polarized electrons into OMTF and as a drain of these spinpolarized electrons from the channel. This problem could be solved by fabrication and investigation of contacts such as Fe(Co,Ni) thin films to an OMTF. In this contribution we present the results of extensive investigations of chemistry and electronic properties of the interface formation between Fe(Co) and the archetypical organic semiconductor copper phthalocyanine (CuPc). The studies were performed by means of core-level and valence-band high-resolution photoemission electron spectroscopy as well as by near-edge X-ray absorption fine structure and using the synchrotron radiation facility ELETTRA (Italy).

  16. Removal of Copper-phthalocyanine from Aqueous Solution by Cationically Templated MCM-41 and MCM-48 Nanoporous Adsorbents

    Institute of Scientific and Technical Information of China (English)

    ANBIA Mansoor; MOHAMMADI Kaveh

    2008-01-01

    The effect of cationic template on the adsorption of copper-phthalocyanine-3,4',4",4'"-tetrasulfonic acid tetra-sodium salt [Cu(tsPc)-4·4Na+] in MCM-41 and MCM-48 mesoporous materials was investigated,using cetyl-trimethylammonium bromide(CTAB)as the cationic template and tetraethyl-orthosilicate as the silica source for synthesis of mesoporous materials.The properties of synthesized samples were characterized with XRD-Iow angle and scanning electron microscopy.The as-synthesized mesoporous samples were used for the separation of Cu(tsPc)tion speed,contact time,composition of adsorbents(presence or absence of surfactants)and initial analyte concen-trations.Adsorption uptakes were rapid on the adsorbents reaching equilibrium in 1/5 h for MCM-48 and 2 h for MCM-41.The materials showed excellent adsorption capacity toward copper-phthalocyanine anion(300.5 mg/g of Cu(tsPc)-4 for as-MCM48 and 285.5 mg/g for as-MCM-41).The materials without surfactant did not show signifi-cant affinity for analyte.Dominant sorption mechanisms were interactions including electrostatic,hydrophobicity,hydrogen bonding and π-π interactions.

  17. Photoemission study of copper phthalocyanine growth on hydrogen-terminated surface: Si(100)2 × 1–H

    Energy Technology Data Exchange (ETDEWEB)

    Ben Hamada, B.; Souissi, A.; Menzli, S.; Arbi, I.; Akremi, A.; Chefi, C. [Université de Carthage, Laboratoire de Physique des Matériaux, Unité de Service Commun Spectromètre de Surfaces, Faculté des Sciences de Bizerte, 7021 Jarzouna, Bizerte (Tunisia); Derivaz, M. [Institut de Science des Matériaux de Mulhouse (IS2M), UMR 7361 CNRS–UHA, Université de Haute Alsace, 3bis rue Alfred Werner, 68093 Mulhouse (France)

    2014-09-30

    Copper phthalocyanine molecules have grown at room temperature under ultra high vacuum on hydrogen-terminated surface Si(100)2 × 1–H. Chemical and electronic properties of the interface were investigated by ultraviolet and X-ray photoemission spectroscopy (UPS, XPS). Results: Results indicated the existence of an interfacial dipole of 0.36 ± 0.05 eV and a band bending of 0.40 ± 0.05 eV. These were evidenced by shifts of XPS core levels and change of the vacuum level position. During the growth, the work function was found to decrease from 4.5 eV for the substrate to 3.74 eV for the highest coverage (40 monolayers). This band bending was also due to the shift of the highest occupied molecular orbital. The interfacial dipole was correlated to a rearrangement of molecules on the surface. An energy level diagram of the interface was deduced from a combination of the XPS and UPS results. - Highlights: • Ultra thin films of cooper phthalocyanine were grown on Si(100)2 × 1–H surface. • Investigation was in situ by UPS, XPS and LEED. • Results indicated the existence of an interfacial dipole and a band bending. • The interfacial dipole was correlated to a rearrangement of molecules on the surface. • An energy level diagram of the interface was deduced.

  18. Synthesis, characterization and femtosecond nonlinear saturable absorption behavior of copper phthalocyanine nanocrystals doped-PMMA polymer thin films

    Science.gov (United States)

    Zongo, S.; Dhlamini, M. S.; Neethling, P. H.; Yao, A.; Maaza, M.; Sahraoui, B.

    2015-12-01

    In this work, we report the femtosecond nonlinear saturable absorption response of synthesized copper phthalocyanine nanocrystals (CPc-NCs)-doped PMMA polymer thin films. The samples were initially characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), UV-Vis and scanning electron microscopy (SEM) techniques. The crystalline phase and morphological analysis revealed nanocrystals of monoclinic structure with an average crystallite size between 31.38 nm and 42.5 nm. The femtosecond Z-scan study at 800 nm central wavelength indicated a saturable absorption behavior of which the mechanism is closely related to the surface plasmon resonance (SPR) of the particles. This nonlinear effect could potentially make the CPc-NCs useful in nonlinear optical devices.

  19. Second harmonic generation at the interface of copper tetra-tert-butyl phthalocyanine Langmuir-Blodgett film/metal

    Institute of Scientific and Technical Information of China (English)

    程晓曼; 姚素薇; 李成全; 间中孝彰; 岩本光正

    2003-01-01

    Optical second harmonic generation (SHG) from the copper tetra-tert-butyl phthalocyanine (CuttbPc) Langmuir-Blodgett (LB) film deposited on a metal-coated glass slide substrate has been investigated. It is considered that the symmetry of the CuttbPc molecule may be broken by the space charge-induced electric field (SCIEF) due to the exchanged charges at the CuttbPc LB film/metal interface. A four-layer model is used to explain the nonlinear optical process in the CuttbPc LB film. The thickness dependence, polarized and incident angle dependence of SHG signal from CuttbPc LB films are calculated. The results of calculation show a good agreement with the experimental data. It is shown that electrostatic phenomena at the interface is correlated closely with SHG signal, and the SHG measurement is also a helpful tool for the detection of the space charge field at the interface.

  20. Passivation of surface states in the ZnO nanowire with thermally evaporated copper phthalocyanine for hybrid photodetectors

    Science.gov (United States)

    Chen, Qi; Ding, Huaiyi; Wu, Yukun; Sui, Mengqiao; Lu, Wei; Wang, Bing; Su, Wenming; Cui, Zheng; Chen, Liwei

    2013-05-01

    The adsorption of O2/H2O molecules on the ZnO nanowire (NW) surface results in the long lifetime of photo-generated carriers and thus benefits ZnO NW-based ultraviolet photodetectors by suppressing the dark current and improving the photocurrent gain, but the slow adsorption process also leads to slow detector response time. Here we show that a thermally evaporated copper phthalocyanine film is effective in passivating surface trap states of ZnO NWs. As a result, the organic/inorganic hybrid photodetector devices exhibit simultaneously improved photosensitivity and response time. This work suggests that it could be an effective way in interfacial passivation using organic/inorganic hybrid structures.The adsorption of O2/H2O molecules on the ZnO nanowire (NW) surface results in the long lifetime of photo-generated carriers and thus benefits ZnO NW-based ultraviolet photodetectors by suppressing the dark current and improving the photocurrent gain, but the slow adsorption process also leads to slow detector response time. Here we show that a thermally evaporated copper phthalocyanine film is effective in passivating surface trap states of ZnO NWs. As a result, the organic/inorganic hybrid photodetector devices exhibit simultaneously improved photosensitivity and response time. This work suggests that it could be an effective way in interfacial passivation using organic/inorganic hybrid structures. Electronic supplementary information (ESI) available: Experimental section includes materials growth, device fabrication, device characterization and the measurement process. Supplementary results and discussion includes electrical properties of the ZnO NW/CuPc device, fitting functions and parameters of photoresponse. See DOI: 10.1039/c3nr01088k

  1. Enhancement in power conversion efficiency in phthalocyanine based photovoltaic cell

    Science.gov (United States)

    Kwong, Chung Yin; Djurisic, Aleksandra B.; Chui, Po C.; Lam, Lillian S. M.; Chan, Wai Kin

    2003-07-01

    The devices studied in this work consist of copper phthalocyanine (CuPc) and fullerene (C60) films between indium tin oxide (ITO) coated substrate as anode and aluminum (Al) as cathode. In order to have optimal performance of heterojunction photovoltaic cell, ITO/CuPc and C60/Al contact should be ohmic. Various ITO treatmetns can be used to improve ITO/CuPc contact. We have compared influence of different ITO treatments on the device performance. We have found that ITO treatmetn yields significant improvement in the performance of CuPc/C60 photovoltaic cells. The short circuit current of teh cell fabricated on ITO substrate with optimal treatment is 9 times larger than that of the cell fabricated on untreated ITO substrate, open circuit voltage has been increased by 0.12V, resulting in 12 times improvement in the power conversion efficiency. The performance of phthalocyanine solar cells can be further improved using a mixed layer structure, ITO/CuPc/CuPc:C60/Al, to increase exciton dissociation efficiency. The mixed layer is fabricated by co-evaporating the materials. For the mixed layer structure, short circuit current has been increased two times compared to the p-n heterojunction cell. This results in 0.16% power conversion efficiency under 98mW/cm2 AM1 solar irradiation.

  2. Synthesis of phthalocyanine doped sol-gel materials

    Science.gov (United States)

    Dunn, Bruce

    1993-01-01

    The synthesis of sol-gel silica materials doped with three different types of metallophthalocyanines has been studied. Homogeneous materials of good optical quality were prepared and the first optical limiting measurements of dyes in sol-gel hosts were carried out. The properties of these solid state limiters are similar to limiters based on phthalocyanine (Pc) in solution. Sol-gel silica materials containing copper, tin and germanium phthalocyanines were investigated. The initial step in all cases was to prepare silica sols by the sonogel method using tetramethoxy silane (TMOS), HCl and distilled water. Thereafter, the synthesis depended upon the specific Pc and its solubility characteristics. Copper phthalocyanine tetrasulfonic acid tetra sodium salt (CuPc4S) is soluble in water and various doping levels (1 x 10 (exp -4) M to 1 x 10 (exp -5) M) were added to the sol. The group IV Pc's, SnPc(OSi(n-hexyl)3)2 and GePc(OSi(n-hexyl)3)2, are insoluble in water and the process was changed accordingly. In these cases, the compounds were dissolved in THF and then added to the sol. The Pc concentration in the sol was 2 x 10(exp -5)M. The samples were then aged and dried in the standard method of making xerogel monoliths. Comparative nanosecond optical limiting experiments were performed on silica xerogels that were doped with the different metallophthalocyanines. The ratio of the net excited state absorption cross section (sigma(sub e)) to the ground state cross section (sigma(sub g)) is an important figure of merit that is used to characterize these materials. By this standard the SnPc sample exhibits the best limiting for the Pc doped sol-gel materials. Its cross section ratio of 19 compares favorably with the value of 22 that was measured in toluene. The GePc materials appear to not be as useful as those containing SnPc. The GePc doped solids exhibit a higher onset energy (2.5 mj and lower cross section ratio, 7. The CuPc4S sol-gel material has a still lower cross

  3. Influence of Exchange-Correlation Functional in the Calculations of Vertical Excitation Energies of Halogenated Copper Phthalocyanines using Time-Dependent Density Functional Theory (TD-DFT)

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Sang Uck [Univ. of Ulsan, Ulsan (Korea, Republic of)

    2013-08-15

    The accurate prediction of vertical excitation energies is very important for the development of new materials in the dye and pigment industry. A time-dependent density functional theory (TD-DFT) approach coupled with 22 different exchange-correlation functionals was used for the prediction of vertical excitation energies in the halogenated copper phthalocyanine molecules in order to find the most appropriate functional and to determine the accuracy of the prediction of the absorption wavelength and observed spectral shifts. Among the tested functional, B3LYP functional provides much more accurate vertical excitation energies and UV-vis spectra. Our results clearly provide a benchmark calibration of the TD-DFT method for phthalocyanine based dyes and pigments used in industry.

  4. An efficient copper phthalocyanine additive of perovskite precursor for improving the photovoltaic performance of planar perovskite solar cells

    Science.gov (United States)

    Wu, Shufang; Liu, Qingwei; Zheng, Ya; Li, Renjie; Peng, Tianyou

    2017-08-01

    Solution processable planar heterojunction perovskite solar cell has drawn much attention as a promising low-cost photovoltaic device, and much effort has been made to improve its power conversion efficiency by choosing appropriate additives for the perovskite precursor solution. Different to those additives reported, a soluble and thermal stable tert-butyl substituted copper phthalocyanine (CuPc(tBu)4) as additive is first introduced into the perovskite precursor solution of a planar perovskite solar cell that is fabricated via the one-step solution process. It is found that the pristine device without CuPc(tBu)4 additive exhibits a power conversion efficiency of 15.3%, while an extremely low concentration (4.4 × 10-3 mM) of CuPc(tBu)4 in the precursor solution leads to the corresponding device achieving an enhanced power conversion efficiency of 17.3%. CuPc(tBu)4 as an additive can improve the quality of perovskite layer with higher crystallinity and surface coverage, then resulting in enhanced light absorption and reduced charge recombination, and thus the better power conversion efficiency. The finding presented here provides a new choice for improving the quality of perovskite layer and the photovoltaic performance of the planar heterojunction perovskite solar cells.

  5. Improved Performance of Fluorinated Copper Phthalocyanine Thin Film Transistors Using Para-hexaphenyl as the Inducing Layer

    Institute of Scientific and Technical Information of China (English)

    MA Feng; WANG Shi-Rong; LI Xiang-Gao; YAN Dong-Hang

    2011-01-01

    We demonstrate n-type organic thin film transistors (OTFTs) employing copper hexadecafluorophthalocyanine (CuPcF16 ) as the active layer and para-hexaphenyl (p-6p) as the inducing layer.Compared with the CuPcF16-based OTFTs without the p-6p inducing layer,the performance of the CuPcF16 /p-6p OTFTs is greatly improved.The charge carrier field-effect mobility μ,on-off current ratio Ion/ Ioff and threshold voltage VT of the CuPcF16/p-6p OTFTs are 0.07cm2/V·s,1.61 × 105 and 6.28 V,respectively,approaching the level of a single crystal device.The improved performance is attributed to the introduction of p-6p to form a highly oriented and continuous film of CuPcF16 with the molecular π-π stack direction parallel to the substrate.Organic thin film transistors have received a wide interest because of their potential applications in displays,logic circuits,sensors and lightemitting devices.[1-4] Although the performance of p-type pentacene-based organic thin film transistors (OTFTs) has reached the α-Si level,[5] the mobility of n-channel OTFTs with air stability is still relatively low.Fluorinated copper phthalocyanine (CuPcF16) is one of a few air-stable n-type organic semiconductors with a low electron field-effect mobility.To improve the performance of CuPcF16-based OTFTs,Yan et al.[5] employed an organic heterojunction buffer layer to decrease the contact resistance of organic/metal.%We demonstrate n-type organic thin film transistors (OTFTs) employing copper hexadecafiuorophthalocyanine (CuPcF16) as the active layer and para-hexaphenyl (p-6p) as the inducing layer. Compared with the CuPcF16-based OTFTs without thep-6p inducing layer, the performance of the CuPcF16/p-6p OTFTs is greatly improved. The charge carrier Reid-effect mobility μ, on-off current ratio Ion/Ioff and threshold voltage Vt of the CuPcF16/p-6p OTFTs are 0.07cm2/V-s, 1.61 x 105 and 6.28 V, respectively, approaching the level of a single crystal device. The improved performance is attributed to

  6. Characterization of copper selenide thin film hole-injection layers deposited at room temperature for use with p-type organic semiconductors

    Science.gov (United States)

    Hiramatsu, Hidenori; Koizumi, Ikue; Kim, Ki-Beom; Yanagi, Hiroshi; Kamiya, Toshio; Hirano, Masahiro; Matsunami, Noriaki; Hosono, Hideo

    2008-12-01

    Copper selenide, CuxSe(x ˜2), was examined as a hole-injection layer for low-temperature organic devices. Crystalline CuxSe films grown at room temperature with atomically flat surfaces exhibited metallic conduction with a high electrical conductivity of 4.5×103 S/cm, a hole concentration of 1.4×1022 cm-3, and a mobility of 2.0 cm2/(V s). Analysis of the free carrier absorption using the Drude model estimated the effective mass of a hole as 1.0me. Photoemission spectroscopy measurements of the interfaces between CuxSe and organic hole transport layers, N ,N'-bis(naphthalen-1-yl)-N ,N'-bis(phenyl) benzidine (NPB) and copper phthalocyanine (CuPc), verified that the hole-injection barriers of these interfaces (0.4 eV for NPB and 0.3 eV for CuPc) are smaller than that of a conventional indium tin oxide (ITO) hole-injection electrode/NPB interface (0.6 eV) but are comparable to that of an ITO electrode/CuPc interface (0.3 eV). Hole-only devices using the CuxSe layer as a hole-injection anode exhibited very low threshold voltages (0.4-0.5 V) and nearly Ohmic characteristics. The NPB layer on the CuxSe layer was found to be highly doped at 1017-1019 cm-3, probably due to copper diffusion, while the CuPc layer is nearly intrinsic with a doping concentration lower than 1015 cm-3. These results indicated that a CuxSe film combined with CuPc is a promising candidate for a low-voltage hole-injection anode or a buffer layer in low-temperature devices such as organic light-emitting diodes and thin film transistors.

  7. Tunable charge transfer properties in metal-phthalocyanine heterojunctions

    Science.gov (United States)

    Siles, P. F.; Hahn, T.; Salvan, G.; Knupfer, M.; Zhu, F.; Zahn, D. R. T.; Schmidt, O. G.

    2016-04-01

    Organic materials such as phthalocyanine-based systems present a great potential for organic device applications due to the possibility of integrating films of different organic materials to create organic heterostructures which combine the electrical capabilities of each material. This opens the possibility to precisely engineer and tune new electrical properties. In particular, similar transition metal phthalocyanines demonstrate hybridization and charge transfer properties which could lead to interesting physical phenomena. Although, when considering device dimensions, a better understanding and control of the tuning of the transport properties still remain in the focus of research. Here, by employing conductive atomic force microscopy techniques, we provide an insight about the nanoscale electrical properties and transport mechanisms of MnPc and fluorinated phthalocyanines such as F16CuPc and F16CoPc. We report a transition from typical diode-like transport mechanisms for pure MnPc thin films to space-charge-limited current transport regime (SCLC) for Pc-based heterostructures. The controlled addition of fluorinated phthalocyanine also provides highly uniform and symmetric-polarized transport characteristics with conductance enhancements up to two orders of magnitude depending on the polarization. We present a method to spatially map the mobility of the MnPc/F16CuPc structures with a nanoscale resolution and provide theoretical calculations to support our experimental findings. This well-controlled nanoscale tuning of the electrical properties for metal transition phthalocyanine junctions stands as key step for future phthalocyanine-based electronic devices, where the low dimension charge transfer, mediated by transition metal atoms could be intrinsically linked to a transfer of magnetic moment or spin.Organic materials such as phthalocyanine-based systems present a great potential for organic device applications due to the possibility of integrating films of

  8. Spectroscopic investigation on the interaction of copper porphyrazines and phthalocyanine with human telomeric G-quadruplex DNA.

    Science.gov (United States)

    Hassani, Leila; Hakimian, Fatemeh; Safaei, Elham

    2014-01-01

    The G-quadruplex DNA is a novel target for anticancer drug discovery and many scientific groups are investigating interaction of small molecules with G-quadruplex DNA to discover therapeutic agents for cancer. Here, interaction of a phthalocyanine (Cu(PcTs)) and two tetrapyridinoporphyrazines ([Cu(2,3-tmtppa)](4+) and [Cu(3,4-tmtppa)](4+)) with Na(+) and K(+) forms of human telomeric G-quadruplex DNA has been investigated by spectroscopic techniques. The results indicated that interaction of the cationic porphyrazines is remarkably stronger than the anionic phthalocyanine and they presumably bind to the G-quadruplex DNA through end-stacking. Fluorescent intercalator displacement assay implied the displacement ability of the complexes with thiazole orange. In addition, circular dichroism spectra of both quadruplex forms converge to the Na(+) isoform after binding to the porphyrazines. In conclusion, the porphyrazines as the complexes that bind to the G-quadruplex DNA, could be suitable candidates for further investigations about inhibition of telomerase enzyme. Copyright © 2013 Elsevier B.V. All rights reserved.

  9. Synthesis, characterization and investigation of electrochemical and spectroelectrochemical properties of non-peripherally tetra-5-methyl-1,3,4-thiadiazole substituted copper(II) iron(II) and oxo-titanium (IV) phthalocyanines

    Science.gov (United States)

    Demirbaş, Ümit; Akyüz, Duygu; Akçay, Hakkı Türker; Barut, Burak; Koca, Atıf; Kantekin, Halit

    2017-09-01

    In this study novel substituted phthalonitrile (3) and non-peripherally tetra 5-Methyl-1,3,4-thiadiazole substituted copper(II) (4), iron(II) (5) and oxo-titanium (IV) (6) phthalocyanines were synthesized. These novel compounds were fully characterized by FT-IR, 1H NMR, UV-vis and MALDI-TOF mass spectroscopic techniques. Voltammetric and in situ spectroelectrochemical measurements were performed for metallo-phthalocyanines (4-6). TiIVOPc and FeIIPc showed metal-based and ligand-based electron transfer reactions while CuIIPc shows only ligand-based electron transfer reaction. Voltammetric measurements indicated that the complexes have reversible, diffusion controlled and one-electron redox reactions. The assignments of the redox processes and color of the electrogenerated species of the complexes were determined with in-situ spectroelectrochemical and electrocolorimetric measurements. These measurements showed that the complexes can be used as the electrochromic materials for various display technologies.

  10. Hydroxyethyl cellulose doped with copper(II) phthalocyanine-tetrasulfonic acid tetrasodium salt as an effective dual functional hole-blocking layer for polymer light-emitting diodes

    Science.gov (United States)

    Wu, Cheng-Liang; Chen, Yun

    2017-07-01

    We report a doping method to improve the performance of solution-processed polymer light-emitting diodes (PLEDs). Doping 12 wt% copper(II) phthalocyanine-tetrasulfonated acid tetrasodium salt (TS-CuPc) into hydroxyethyl cellulose (HEC) as a dual functional hole-blocking layer (df-HBL) of multilayer PLED (glass/ITO/PEDOT:PSS/HY-PPV/TS-CuPc-doped HEC/LiF/Al) significantly enhanced maximum luminance, maximum current and power efficiency over that without the df-HBL (10,319 cd/m2, 2.98 cd/A and 1.24 lm/W) to (29,205 cd/m2, 13.27 cd/A and 9.56 lm/W). CV measurements reveal that HEC possesses a powerful hole-blocking capability. Topography and conductivity AFM images show that doping TS-CuPc increases the interfacial contact area and interfacial conductivity, which can overcome the insulating nature of HEC and thus further facilitate electron injection. Enhancements in device performance are attributed to the improved carrier balance and recombination in the presence of df-HBL, confirmed in electron-only and hole-only devices. Moreover, apparently raised open-circuit voltages provide further evidence that enhanced electron injection is indeed realized by the df-HBL. This study demonstrates an effective approach to develop highly efficient PLEDs.

  11. Multi-orbital non-crossing approximation from maximally localized Wannier functions: the Kondo signature of copper phthalocyanine on Ag(100)

    Energy Technology Data Exchange (ETDEWEB)

    Korytar, Richard; Lorente, Nicolas, E-mail: rkorytar@cin2.es [Centro de investigacion en nanociencia y nanotecnologIa (CSIC-ICN), Campus de la UAB, E-08193 Bellaterra (Spain)

    2011-09-07

    We have developed a multi-orbital approach to compute the electronic structure of a quantum impurity using the non-crossing approximation. The calculation starts with a mean-field evaluation of the system's electronic structure using a standard quantum chemistry code; here we use density functional theory (DFT). We transformed the one-electron structure into an impurity Hamiltonian by using maximally localized Wannier functions. Hence, we have developed a method to study the Kondo effect in systems based on an initial one-electron calculation. We have applied our methodology to a copper phthalocyanine molecule chemisorbed on Ag(100), and we have described its spectral function for three different cases where the molecule presents a single spin or two spins with ferro- and anti-ferromagnetic exchange couplings. We find that the use of broken-symmetry mean-field theories such as Kohn-Sham DFT cannot deal with the complexity of the spin of open-shell molecules on metal surfaces and extra modeling is needed. (paper)

  12. The complex nature of phthalocyanine/gold interfaces

    Energy Technology Data Exchange (ETDEWEB)

    Lindner, Susi, E-mail: s.wintz@ifw-dresden.de [IFW Dresden, P.O. Box 270116, D-01171 Dresden (Germany); Treske, Uwe; Knupfer, Martin [IFW Dresden, P.O. Box 270116, D-01171 Dresden (Germany)

    2013-02-15

    We compare the electronic properties of the interface between Au(1 0 0) and cobalt phthalocyanine (CoPc), fluorinated F{sub 16}CoPc as well as CuPc using X-ray photoemission spectroscopy and valence band ultra-violet photoemission spectroscopy. Our results show that in addition to the formation of an interface dipole at the interfaces of CoPc and F{sub 16}CoPc to gold, there is a local charge transfer to the central Co ion, which as a result is reduced to Co(I).

  13. Understanding the Adsorption of CuPc and ZnPc on Noble Metal Surfaces by Combining Quantum-Mechanical Modelling and Photoelectron Spectroscopy

    Directory of Open Access Journals (Sweden)

    Yu Li Huang

    2014-03-01

    Full Text Available Phthalocyanines are an important class of organic semiconductors and, thus, their interfaces with metals are both of fundamental and practical relevance. In the present contribution we provide a combined theoretical and experimental study, in which we show that state-of-the-art quantum-mechanical simulations are nowadays capable of treating most properties of such interfaces in a quantitatively reliable manner. This is shown for Cu-phthalocyanine (CuPc and Zn-phthalocyanine (ZnPc on Au(111 and Ag(111 surfaces. Using a recently developed approach for efficiently treating van der Waals (vdW interactions at metal/organic interfaces, we calculate adsorption geometries in excellent agreement with experiments. With these geometries available, we are then able to accurately describe the interfacial electronic structure arising from molecular adsorption. We find that bonding is dominated by vdW forces for all studied interfaces. Concomitantly, charge rearrangements on Au(111 are exclusively due to Pauli pushback. On Ag(111, we additionally observe charge transfer from the metal to one of the spin-channels associated with the lowest unoccupied π-states of the molecules. Comparing the interfacial density of states with our ultraviolet photoelectron spectroscopy (UPS experiments, we find that the use of a hybrid functionals is necessary to obtain the correct order of the electronic states.

  14. Synthesis, aggregation and spectroscopic studies of novel water soluble metal free, zinc, copper and magnesium phthalocyanines and investigation of their anti-bacterial properties

    Science.gov (United States)

    Bayrak, Rıza; Akçay, Hakkı Türker; Beriş, Fatih Şaban; Şahin, Ertan; Bayrak, Hacer; Demirbaş, Ümit

    2014-12-01

    In this study, novel phthalonitrile derivative (3) was synthesized by the reaction between 4-nitrophthalonitrile (2) and a triazole derivative (1) containing pyridine moiety. Crystal structure of compound (3) was characterized by X-ray diffraction. New metal free and metallo-phthalocyanine complexes (Zn, Cu, and Mg) were synthesized using the phthalonitrile derivative (3). Cationic derivatives of these phthalocyanines (5, 7, 9, and 11) were prepared from the non-ionic phthalocyanines (4, 6, 8, and 10). All proposed structures were supported by instrumental methods. The aggregation behaviors of the phthalocyanines (4-11) were investigated in different solvents such as dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF), chloroform and water. Water soluble cationic Pcs (5, 7, 9, and 11) aggregated in water and sodium dodecyl sulfate was used to prevent the aggregation. The second derivatives of the UV-Vis spectra of aggregated Pcs were used for analyzing the Q and B bands of aggregated species. Thermal behaviors of the phthalocyanines were also studied. In addition, anti-bacterial properties of the phthalocyanines were investigated. We used four gram negative and two gram positive bacteria to determine antibacterial activity of these compounds. Compound 7 has the best activity against the all bacteria with 125 μg/mL of MIC value. Compounds 4, 6, and 10 have the similar effect on the bacteria with 250 μg/mL of MIC value.

  15. Salicylate-selective Potential Response of an Electrode Based on a Copper(Ⅱ)-phthalocyanine Derivative as an Ionophore

    Institute of Scientific and Technical Information of China (English)

    XU Wenju; YUAN Ruo; CHAI Yaqin

    2009-01-01

    Selectivity properties were established for salicylate-selective electrodes prepared by incorporating 2,9,16,23-copper(Ⅱ)-tetranitrophthalocyanine (Cu(Ⅱ)TNPc) and 2,9,16,23-copper(Ⅱ)-tetraaminophthalocyanine (Cu(Ⅱ)TAPc) into plasticized poly(vinyl chloride) (PVC) membranes. The effect of nature of plasticizer, concentrations of iono-phore and anionic and cationic additives on the potential response of the electrode was investigated. The PVC membrane electrode based on Cu(Ⅱ)TNPc exhibited preferential selectivity for salicylate (Sal-) over other tested anions. The best potential response characteristics of a wide working concentration range 1.0×10-1-9.0×10-7 the membrane containing (w/w) 3.0% Cu(II)TNPc, 67.0% o-NPOE, 29.5% PVC, and 0.5% NaTPB. The proposed electrode with good stability and fast response could be used over a pH range of 3.0-7.0. And it was successfully applied to the determination of salicylate in actual samples with satisfactory results.

  16. Photophysical studies of newly derivatized mono substituted phthalocyanines grafted onto silica nanoparticles via click chemistry

    Science.gov (United States)

    Fashina, Adedayo; Amuhaya, Edith; Nyokong, Tebello

    2015-04-01

    This work reports on the synthesis, characterization and photophysical studies of newly derived phthalocyanine complexes and the phthalocyanine-silica nanoparticles conjugates. The derived phthalocyanine complexes have one terminal alkyne group. The derived phthalocyanine complexes showed improved photophysical properties (ФF, ФT, ΦΔ and τT) compared to the respective phthalocyanine complexes from which they were derived. The derived phthalocyanine complexes were conjugated to the surface of an azide functionalized silica nanoparticles via copper (1) catalyzed cyclo-addition reaction. All the conjugates showed lower triplet quantum yields ranging from 0.37 to 0.44 compared to the free phthalocyanine complexes. The triplet lifetimes ranged from 352 to 484 μs for the conjugates and from 341 to 366 μs for the free phthalocyanine complexes.

  17. Efficient On-Off Ratiometric Fluorescence Probe for Cyanide Ion Based on Perturbation of the Interaction between Gold Nanoclusters and a Copper(II)-Phthalocyanine Complex.

    Science.gov (United States)

    Shojaeifard, Zahra; Hemmateenejad, Bahram; Shamsipur, Mojtaba

    2016-06-22

    A new ratiometric fluorescent sensor was developed for the sensitive and selective detection of cyanide ion (CN(-)) in aqueous media. The ratiometric sensing system is based on CN(-) modulated recovery of copper(II) phthalocyanine (Cu(PcTs)) fluorescence signal at the expense of diminished fluorescence intensity of gold nanoclusters (AuNCs). Preliminary experiments revealed that the AuNCs and Cu(PcTs) possess a turn-off effect on each other, the interaction of which being verified through studying their interactions by principle component analysis (PCA) and multivariate cure resolution-alternating least-squares (MCR-ALS) methods. In the presence of CN(-) anion, the AuNCs and Cu(PcTs) interaction was perturbed, so that the fluorescence of Cu (PcTs), already quenched by AuNCs, was found to be efficiently recovered, while the fluorescence intensity of AuNCs was quenched via the formation of a stable [Au(CN)2](-) species. The ratiometric variation of AuNCs and Cu(PcTs) fluorescence intensities leads to designing a highly sensitive probe for CN(-) ion detection. Under the optimal conditions, CN(-) anion was detected without needing any etching time, over the concentration range of 100 nM-220 μM, with a detection limit of 75 nM, which is much lower than the allowable level of CN(-) in water permitted by the World Health Organization (WHO). Moreover, the detection of CN(-) was developed based on the CN(-) effects on the blue and red florescent colors of Cu(PcTs) and AuNCs, respectively. The designed probe displays a continuous color change from red to blue by addition of CN(-), which can be clearly observed by the naked eye in the range of 7-350 μM, under UV lamp. The prepared AuNCs/Cu(PcTs) probe was successfully utilized for the selective and sensitive determination of CN(-) anion in two different types of natural water (Rodbal dam and rainwater) and also in blood serum as a biological sample.

  18. Functionalization of nanocrystalline diamond films with phthalocyanines

    Energy Technology Data Exchange (ETDEWEB)

    Petkov, Christo [Institute of Nanostructure Technologies and Analytics (INA), Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel (Germany); Reintanz, Philipp M. [Institute of Chemistry, Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel (Germany); Kulisch, Wilhelm [Institute of Nanostructure Technologies and Analytics (INA), Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel (Germany); Degenhardt, Anna Katharina [Institute of Chemistry, Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel (Germany); Weidner, Tobias [Max Planck Institute for Polymer Research, Mainz (Germany); Baio, Joe E. [School of Chemical, Biological and Environmental Engineering, Oregon State University, Corvallis, OR (United States); Merz, Rolf; Kopnarski, Michael [Institut für Oberflächen- und Schichtanalytik (IFOS), Kaiserslautern (Germany); Siemeling, Ulrich [Institute of Chemistry, Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel (Germany); Reithmaier, Johann Peter [Institute of Nanostructure Technologies and Analytics (INA), Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel (Germany); Popov, Cyril, E-mail: popov@ina.uni-kassel.de [Institute of Nanostructure Technologies and Analytics (INA), Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel (Germany)

    2016-08-30

    Highlights: • Grafting of phthalocyanines on nanocrystalline diamond films with different terminations. • Pc with different central atoms and side chains synthesized and characterized. • Attachment of Pc on H- and O-terminated NCD studied by XPS and NEXAFS spectroscopy. • Orientation order of phthalocyanine molecules on NCD surface. - Abstract: Phthalocyanine (Pc) derivatives containing different central metal atoms (Mn, Cu, Ti) and different peripheral chains were synthesized and comprehensively characterized. Their interaction with nanocrystalline diamond (NCD) films, as-grown by hot-filament chemical vapor deposition or after their modification with oxygen plasma to exchange the hydrogen termination with oxygen-containing groups, was studied by X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. The elemental composition as determined by XPS showed that the Pc were grafted on both as-grown and O-terminated NCD. Mn, Cu and Ti were detected together with N stemming from the Pc ring and S in case of the Ti-Pc from the peripheral ligands. The results for the elemental surface composition and the detailed study of the N 1s, S 2p and O 1s core spectra revealed that Ti-Pc grafted better on as-grown NCD but Cu-Pc and Mn-Pc on O-terminated films. Samples of Mn-Pc on as-grown and O-terminated NCD were further investigated by NEXAFS spectroscopy. The results showed ordering of the grafted molecules, laying flat on the H-terminated NCD surface while only the macrocycles were oriented parallel to the O-terminated surface with the peripheral chains perpendicular to it.

  19. Optoelectronic properties of CuPc thin films deposited at different substrate temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Della Pirriera, M; Puigdollers, J; Voz, C; Alcubilla, R [Micro and Nanotechnology Group. Dept. Enginyeria Electronica, Universitat Politecnica Catalunya, 08034 Barcelona (Spain); Stella, M; Bertomeu, J [Dep. Fisica Aplicada i Optica. Universitat de Barcelona (Spain)

    2009-07-21

    Structural and optical characterization of copper phthalocyanine thin film thermally deposited at different substrate temperatures was the aim of this work. The morphology of the films shows strong dependence on temperature, as can be observed by atomic force microscopy and x-ray diffraction spectroscopy, specifically in the grain size and features of the grains. The increase in the crystal phase with substrate temperature is shown by x-ray diffractometry. Optical absorption coefficient measured by photothermal deflection spectroscopy and optical transmittance reveal a weak dependence on the substrate temperature. Besides, the electro-optical response measured by the external quantum efficiency of Schottky ITO/CuPc/Al diodes shows an optimized response for samples deposited at a substrate temperature of 60 deg. C, in correspondence to the I-V diode characteristics.

  20. Glycosylated Metal Phthalocyanines

    Directory of Open Access Journals (Sweden)

    Michael Hanack

    2015-11-01

    Full Text Available In the first part; the syntheses of mono-; di-; and tetra-glycosylated phthalonitriles is described; which are the most used starting materials for the preparation of the corresponding glycosylated metal (mostly zinc phthalocyanines. In the second section; the preparation of symmetric and unsymmetric mono-; tetra-; and octa- glycosylated zinc phthalocyanines are reviewed; in which the sugar is attached to the phthalocyanine macrocycle; either anomerically or via another one of its OH-groups.

  1. Memory effects in a Al/Ti:HfO2/CuPc metal-oxide-semiconductor device

    Science.gov (United States)

    Tripathi, Udbhav; Kaur, Ramneek

    2016-05-01

    Metal oxide semiconductor structured organic memory device has been successfully fabricated. Ti doped hafnium oxide (Ti:HfO2) nanoparticles has been fabricated by precipitation method and further calcinated at 800 °C. Copper phthalocyanine, a hole transporting material has been utilized as an organic semiconductor. The electrical properties of the fabricated device have been studied by measuring the current-voltage and capacitance-voltage characteristics. The amount of charge stored in the nanoparticles has been calculated by using flat band condition. This simple approach for fabricating MOS memory device has opens up opportunities for the development of next generation memory devices.

  2. Memory effects in a Al/Ti:HfO{sub 2}/CuPc metal-oxide-semiconductor device

    Energy Technology Data Exchange (ETDEWEB)

    Tripathi, Udbhav, E-mail: udbhav1781996@gmail.com; Kaur, Ramneek [Department of Physics, Center of Advanced Study in Physics, Panjab University, Chandigarh-160 014 (India)

    2016-05-23

    Metal oxide semiconductor structured organic memory device has been successfully fabricated. Ti doped hafnium oxide (Ti:HfO{sub 2}) nanoparticles has been fabricated by precipitation method and further calcinated at 800 °C. Copper phthalocyanine, a hole transporting material has been utilized as an organic semiconductor. The electrical properties of the fabricated device have been studied by measuring the current-voltage and capacitance-voltage characteristics. The amount of charge stored in the nanoparticles has been calculated by using flat band condition. This simple approach for fabricating MOS memory device has opens up opportunities for the development of next generation memory devices.

  3. Spin-polarized scanning tunneling microscopy of magnetic nanostructures at the example of bcc-Co/Fe(110), Fe/Mo(110), and copper phthalocyanine/Fe(1110); Spinpolarisierte Rastertunnelmikroskopie magnetischer Nanostrukturen am Beispiel von bcc-Co/Fe(110), Fe/Mo(110) und Kupfer-Phthalocyanin/Fe(110)

    Energy Technology Data Exchange (ETDEWEB)

    Methfessel, Torsten

    2010-12-09

    This thesis provides an introduction into the technique of spin-polarized scanning tunnelling microscopy and spectroscopy as an experimental method for the investigation of magnetic nanostructures. Experimental results for the spin polarized electronic structure depending on the crystal structure of ultrathin Co layers, and depending on the direction of the magnetization for ultrathin Fe layers are presented. High-resolution measurements show the position-dependent spin polarization on a single copper-phthalocyanine molecule deposited on a ferromagnetic surface. Co was deposited by molecular beam epitaxy on the (110) surface of the bodycentered cubic metals Cr and Fe. In contrast to previous reports in the literature only two layers of Co can be stabilized in the body-centered cubic (bcc) structure. The bcc-Co films on the Fe(110) surface show no signs of epitaxial distortions. Thicker layers reconstruct into a closed-packed structure (hcp / fcc). The bcc structure increases the spin-polarization of Co to P=62 % in comparison to hcp-Co (P=45 %). The temperature-dependent spin-reorientation of ultrathin Fe/Mo(110) films was investigated by spin-polarized spectroscopy. A reorientation of the magnetic easy axis from the [110] direction along the surface normal to the in-plane [001] axis is observed at T (13.2{+-}0.5) K. This process can be identified as a discontinuous reorientation transition, revealing two simultaneous minima of the free energy in a certain temperature range. The electronic structure of mono- and double-layer Fe/Mo(110) shows a variation with the reorientation of the magnetic easy axis and with the direction of the magnetization. The investigation of the spin-polarized charge transport through a copper-phthalocyanine molecule on the Fe/Mo(110) surface provides an essential contribution to the understanding of spin-transport at the interface between metal and organic molecule. Due to the interaction with the surface of the metal the HOMO-LUMO energy

  4. Synthesis, Characterization and Photoelectric Properties of the Copper Phthalocyanine-modied Multi-walled Carbon Nanotubes%多壁碳纳米管-酞菁铜复合物的合成表征及光电性能

    Institute of Scientific and Technical Information of China (English)

    吴振奕; 杨绳岩

    2011-01-01

    采用氯磺酸作为磺化试剂,在多壁碳纳米管上接枝氯磺酰基,之后通过乙二胺的胺解反应,制备出胺基修饰的多壁碳纳米管MWCNT-NH2,并进一步与氯磺酰基酞菁铜反应制备出MWCNT-Pc复合物.产物采用红外光谱,紫外可见,拉曼光谱,X射线光电子能谱,循环伏安,热重分析等进行了表征.结果表明,MWCNT-NH2上磺酰胺基接枝在MWCNT表面,而MWCNT-Pc上的酞菁基团是通过MWCNT-NH2上的酰胺基团与Pc形成复合物,碳纳米管上约38个碳原子结合一个磺酸基酞菁分子;该MWCNT-Pc复合物的热稳定性较MWCNT-NH2低;利用喷涂法构筑了ITO/MWCNT-Pc光电极,光电性能的研究结果表明在AM1.5光照条件下,光电压及光电流分别为0.434V和0.158mA/cm2;在320nm处的IPCE达19.8%,具有较优良的光电转化性能.根据测得的MWCNT-Pc的能带结构,推知MWCNT-Pc的光诱导电子转移过程是Pc端基发生光激发电子跃迁,此后电子转移到MWCNTs上并进一步传递到ITO,完成电荷分离.%Multi-walled carbon nanotubes (MWCNTs) were grafted with sulfonyl chloride groups using chlorosulfonic acid as a sulfonation reagent, and then the amino-modified multi-walled carbon nanotubes of MWCNT-NH2 was prepared via the aminolysis reaction. The MWCNT-NH2 was further reacted with copper phthalocyanine sulfonyl chloride to prepared the complex of MWCNT-Pc. The products were fully characterized by various standard analytical techniques, including scanning electron microscope, transmission electron microscope, infrared spectroscope, UV-Vis absorption spectroscope, Raman spectroscope, X-ray photoelectron spectroscope, thermogravimetric analysis, and cyclic voltammetry. The results indicated that the complex of MWCNT-Pc was fabricated through covalent assembly of MWCNT-NH2 with copper phthalocyanine, with a copper phthalocyanine molecule for every 38 MWCNT carbons.The thermal stability of the complex of MWCNT-Pc was lower than that of MWCNT-NH2.The

  5. Functionalization of nanocrystalline diamond films with phthalocyanines

    Science.gov (United States)

    Petkov, Christo; Reintanz, Philipp M.; Kulisch, Wilhelm; Degenhardt, Anna Katharina; Weidner, Tobias; Baio, Joe E.; Merz, Rolf; Kopnarski, Michael; Siemeling, Ulrich; Reithmaier, Johann Peter; Popov, Cyril

    2016-08-01

    Phthalocyanine (Pc) derivatives containing different central metal atoms (Mn, Cu, Ti) and different peripheral chains were synthesized and comprehensively characterized. Their interaction with nanocrystalline diamond (NCD) films, as-grown by hot-filament chemical vapor deposition or after their modification with oxygen plasma to exchange the hydrogen termination with oxygen-containing groups, was studied by X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. The elemental composition as determined by XPS showed that the Pc were grafted on both as-grown and O-terminated NCD. Mn, Cu and Ti were detected together with N stemming from the Pc ring and S in case of the Ti-Pc from the peripheral ligands. The results for the elemental surface composition and the detailed study of the N 1s, S 2p and O 1s core spectra revealed that Ti-Pc grafted better on as-grown NCD but Cu-Pc and Mn-Pc on O-terminated films. Samples of Mn-Pc on as-grown and O-terminated NCD were further investigated by NEXAFS spectroscopy. The results showed ordering of the grafted molecules, laying flat on the H-terminated NCD surface while only the macrocycles were oriented parallel to the O-terminated surface with the peripheral chains perpendicular to it.

  6. Vectorial diffusion for facile solution-processed self-assembly of insoluble semiconductors: a case study on metal phthalocyanines.

    Science.gov (United States)

    Wang, Chengliang; Fang, Yaoguo; Wen, Liaoyong; Zhou, Min; Xu, Yang; Zhao, Huaping; De Cola, Luisa; Hu, Wenping; Lei, Yong

    2014-08-25

    Solution processibility is one of the most intriguing properties of organic semiconductors. However, it is difficult to find a suitable solvent and solution process for most semiconductors. For example, metal phthalocyanines (MPcs) are only soluble in non-volatile solvents, which prevent their applications from solution process. For the first time, vectorial diffusion is utilized for solution processing of MPcs. The obtained large F16CuPc and α-phase CuPc crystals and the efficient phase separation of them suggest the vectorial diffusion process is as slow as a self-assembly process, which is helpful to yield large crystals and purify the semiconductors. This method, which only uses common commercial solvents without any complex and expensive instruments and high-temperature operation, provides a facile approach for purification of organic semiconductors and growth of their crystals in large quantities.

  7. Tetra methyl substituted Cu(II) phthalocyanine as alternative hole transporting material for organometal halide perovskite solar cells

    Science.gov (United States)

    Sfyri, Georgia; Kumar, Challuri Vijay; Wang, Yu-Long; Xu, Zong-Xiang; Krontiras, C. A.; Lianos, Panagiotis

    2016-01-01

    Copper phthalocyanine is a promising hole transporting material, which can be employed with solid state perovskite solar cells. Tetra methyl substituted copper phthalocyanine was presently studied as a hole transporting material and demonstrated improved performance with respect to unsubstituted copper phthalocyanine. This material shows a strong absorption in the Visible and Near IR part of the electromagnetic spectrum contributing to the absorption of photons. Its LUMO and HOMO level are favourably positioned for injecting electrons and scavenging holes. Methyl substitution facilitates closer molecular packing leading to a stronger extinction coefficient, stronger Ͽ⿿Ͽ interaction and higher charge carrier mobility.

  8. Controlling the Orbital Sequence in Individual Cu-Phthalocyanine Molecules

    NARCIS (Netherlands)

    Uhlmann, C.; Swart, I.; Repp, J.

    2013-01-01

    We report on the controlled change of the energetic ordering of molecular orbitals. Negatively charged copper(II)phthalocyanine on NaCl/Cu(100) undergoes a Jahn–Teller distortion that lifts the degeneracy of two frontier orbitals. The energetic order of the levels can be controlled by Au and Ag atom

  9. Controlling the Orbital Sequence in Individual Cu-Phthalocyanine Molecules

    NARCIS (Netherlands)

    Uhlmann, C.; Swart, I.; Repp, J.

    2013-01-01

    We report on the controlled change of the energetic ordering of molecular orbitals. Negatively charged copper(II)phthalocyanine on NaCl/Cu(100) undergoes a Jahn–Teller distortion that lifts the degeneracy of two frontier orbitals. The energetic order of the levels can be controlled by Au and Ag

  10. Aqueous aerobic oxidation of alkyl arenes and alcohols catalyzed by copper(II) phthalocyanine supported on three-dimensional nitrogen-doped graphene at room temperature.

    Science.gov (United States)

    Mahyari, Mojtaba; Laeini, Mohammad Sadegh; Shaabani, Ahmad

    2014-07-25

    Copper(ii) tetrasulfophthalocyanine supported on three-dimensional nitrogen-doped graphene-based frameworks was synthesized and introduced as a bifunctional catalyst for selective aerobic oxidation of alkyl arenes and alcohols to the corresponding carbonyl compounds. The ease of catalyst separation, high turnover, low catalyst loading and recyclability could potentially render it applicable in industrial setting.

  11. Electronic Processes in Phthalocyanine Solids

    Institute of Scientific and Technical Information of China (English)

    汪茫; 陈红征; 沈菊李; 杨士林

    1994-01-01

    The positive or negative photoconductivity effects are found between the component of phthalocyanine dimixing composites and the photoconductivity by dimixing method. The relations between the crystalline forms and electronic structure of the composites and the photoconductivity are further studied through X-ray and XPS. The results indicate that the composites may be a kind of new uniform eutectic composites, which can enhance or reduce the partial charge transfer processes from phthalocyanine rings to metals, and the processes are exactly correspondent with the positive or negative photoconductivity effects. A model of gradually transferred charge in the phthalocyanine solids is put forward, which can better explain the electronic processes in the phthalocyanine solids.

  12. Hierarchical nanostructures of copper(II) phthalocyanine on electrospun TiO(2) nanofibers: controllable solvothermal-fabrication and enhanced visible photocatalytic properties.

    Science.gov (United States)

    Zhang, Mingyi; Shao, Changlu; Guo, Zengcai; Zhang, Zhenyi; Mu, Jingbo; Cao, Tieping; Liu, Yichun

    2011-02-01

    In the present work, 2,9,16,23-tetranitrophthalocyanine copper(II) (TNCuPc)/TiO(2) hierarchical nanostructures were successfully fabricated by a simple combination method of electrospinning technique and solvothermal processing. Scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) spectroscopy, X-ray diffraction (XRD), UV-vis diffuse reflectance (DR), Fourier transform infrared spectrum (FT-IR), X-ray photoelectron spectroscopy (XPS), and thermal gravimetric and differential thermal analysis (TG-DTA) were used to characterize the as-synthesized TNCuPc/TiO(2) hierarchical nanostructures. The results showed that the secondary TNCuPc nanostructures were not only successfully grown on the primary TiO(2) nanofibers substrates but also uniformly distributed without aggregation. By adjusting the solvothermal fabrication parameters, the TNCuPc nanowires or nanoflowers were facilely fabricated, and also the loading amounts of TNCuPc could be controlled on the TNCuPc/TiO(2) hierarchical nanostructural nanofibers. And, there might exist the interaction between TNCuPc and TiO(2). A possible mechanism for the formation of TNCuPc/TiO(2) hierarchical nanostructures was suggested. The photocatalytic studies revealed that the TNCuPc/TiO(2) hierarchical nanostructures exhibited enhanced photocatalytic efficiency of photodegradation of Rhodamine B (RB) compared with the pure TNCuPc or TiO(2) nanofibers under visible-light irradiation.

  13. Ambipolar charge carrier transport in organic semiconductor blends of C{sub 60} and CuPc; Ambipolarer Ladungstransport in organischen Halbleiter-Mischschichten bestehend aus C{sub 60} und CuPc

    Energy Technology Data Exchange (ETDEWEB)

    Bronner, Markus

    2008-06-20

    In this work ambipolar charge carrier transport is realised in organic field effect transistors using mixtures of p-conductive copper phthalocyanine and n-conductive buckminster fullerene as active layer. These blends are known from research on organic solar cells and can be considered as a model system for ambipolar transport. The field effect mobilities for electrons and holes can be adjusted by the variation of the mixing ratio. Thereby balanced mobilities for both charge carrier types are possible. In this work the variation of mobility, threshold voltage and electronic energy levels with the mixing ratio is discussed. The charge carrier mobilities are strongly reduced upon dilution of the respective conducting phase by the other species. This shows that transport of each carrier species occurs by percolation through the respective phase in the blend. A strong correlation between contact resistance and mobility indicates that carrier injection is diffusion limited. A charge redistribution in the copper phthalocyanine causes a hole accumulation at the organic/organic interface and affects thereby the threshold voltage for holes. The electronic structure was investigated by photoelectron spectroscopy. It was found that there is no chemical reaction between the different materials. The common work function of these blends changes linearly between the work functions of the neat materials. Moreover, a constant ionisation potential for the highest occupied molecular orbitals of the two materials and the core levels is obtained. Furthermore ambipolar inverters using mixed organic semiconductor layers were made and compared to complementary inverters consisting of discrete p- and n-channel transistors. The experimental findings and concomitant simulations demonstrate the need for balanced electron and hole mobilities in order to achieve symmetric inverter characteristics. However, they also reveal the superior performance of true complementary logic inverters towards

  14. Method of solubilizing phthalocyanines and metallophthalocyanines

    Energy Technology Data Exchange (ETDEWEB)

    Rathke, J.W.; Chen, M.J.; Fendrick, C.M.

    1990-06-01

    A one-step method of manufacturing soluble phthalocyanines and metallophthalocyanines, like zinc phthalocyanine, by converting a phthalocyanine or a metallophthalocyanine to a trialkylsilyl-substituted derivative is disclosed. The phthalocyanine or metallophthalocyanine is converted to a soluble trialkylsilyl-substituted derivative by interacting the phthalocyanine or metallophthalocyanine with an active metal amide, like lithium 2,2,6, 6-tetra-methylpiperidide, and a halotrialkylsilane, like chlorotrimethylsilane, to provide a phthalocyanine compound, like phthalocyanine monomers, dimers or polymers, metalated or unmetalated, that are soluble in organic media.

  15. High-efficiency THz modulator based on phthalocyanine-compound organic films

    Energy Technology Data Exchange (ETDEWEB)

    He, Ting; Zhang, Bo, E-mail: bzhang@cnu.edu.cn, E-mail: sjl-phy@cnu.edu.cn; Shen, Jingling, E-mail: bzhang@cnu.edu.cn, E-mail: sjl-phy@cnu.edu.cn; Zang, Mengdi; Chen, Tianji [Beijing Key Laboratory for Terahertz Spectroscopy and Imaging, Key Laboratory of Terahertz Optoelectronics, Ministry of Education, Department of Physics, Capital Normal University, Beijing 100048 (China); Hu, Yufeng; Hou, Yanbing [Key Laboratory of Luminescence and Optical Information, Ministry of Education, Institute of Optoelectronic Technology, Beijing Jiaotong University, Beijing 100044 (China)

    2015-02-02

    We report a high efficiency, broadband terahertz (THz) modulator following a study of phthalocyanine-compound organic films irradiated with an external excitation laser. Both transmission and reflection modulations of each organic/silicon bilayers were measured using THz time-domain and continuous-wave systems. For very low intensities, the experimental results show that AlClPc/Si can achieve a high modulation factor for transmission and reflection, indicating that AlClPc/Si has a superior modulation efficiency compared with the other films (CuPc and SnCl{sub 2}Pc). In contrast, the strong attenuation of the transmitted and reflected THz waves revealed that a nonlinear absorption process takes place at the organic/silicon interface.

  16. Photoelectron spectroscopy of phthalocyanine vapors

    Energy Technology Data Exchange (ETDEWEB)

    Berkowitz, J.

    1979-01-01

    The He(I) photoelectron spectra of several metal phthalocyanines and metal-free phthalocyanine vapor shows that: a sharp peak at 4.99 eV is an artifact due to ionization of atomic He by He(II) radiation; the first phthalocyanine peak (metal-containing or metal-free) occurs at 6.4 eV; and the metal-like d orbitals lie at least 1 to 2 eV deeper, except in the case of Fe. (DLC)

  17. Covalentely Attached Multilayer Films Comprising Phthalocyanine and Their Photoelectron Conversion Properties

    Institute of Scientific and Technical Information of China (English)

    ZANG Mao-feng; YAO Qiao-hong; YANG Zhao-hui; HUANG Chun-hui; CAO Wei-xiao

    2004-01-01

    The photosensitive multilayer films from sulfonated metal-free, sulfonated copper-, and sulfonated nickel-phthalocyanines were fabricated with diazoresin layer by layer on a substrate via electrostatic interaction by the self-assembly technique. Under UV irradiation, the linkage nature between the layers of the film is converted from the electrostatic bonding to covalent bonding. The covalently attached multilayer films are very stable towards polar solvents and salt aqueous solutions. The photovoltaic properties of the covalently attached film can be determined by means of a traditional three-electrode photoelectrochemical cell in aqueous solutions with KCl as the supporting electrolyte. The photocurrent determination has shown that the sulfonated copper-containing phthalocyanine films possess a higher photocurrent value than sulfonated metalfree and sulfonated nickel-containing phthalocyanine films.

  18. Ambipolar Cu- and Fe-phthalocyanine single-crystal field-effect transistors

    NARCIS (Netherlands)

    De Boer, R.W.I.; Stassen, A.F.; Craciun, M.F.; Mulder, C.L.; Molinari, A.; Rogge, S.; Morpurgo, A.F.

    2005-01-01

    We report the observation of ambipolar transport in field-effect transistors fabricated on single crystals of copper- and iron-phthalocyanine, using gold as a high work-function metal for the fabrication of source and drain electrodes. In these devices, the room-temperature mobility of holes reaches

  19. Metal (2) 4,4',4",4'" phthalocyanine tetraamines as curing agents for epoxy resins

    Science.gov (United States)

    Achar, B. N.; Fohlen, G. M.; Parker, J. A. (Inventor)

    1985-01-01

    Metal, preferably divalent copper, cobalt or nickel, phthalocyanine tetraamines are used as curing agents for epoxides. The resulting copolymers have high thermal and chemical resistance and are homogeneous. They are useful as binders for laminates, e.g., graphite cloth laminate.

  20. Ambipolar Cu- and Fe-phthalocyanine single-crystal field-effect transistors

    NARCIS (Netherlands)

    De Boer, R.W.I.; Stassen, A.F.; Craciun, M.F.; Mulder, C.L.; Molinari, A.; Rogge, S.; Morpurgo, A.F.

    2005-01-01

    We report the observation of ambipolar transport in field-effect transistors fabricated on single crystals of copper- and iron-phthalocyanine, using gold as a high work-function metal for the fabrication of source and drain electrodes. In these devices, the room-temperature mobility of holes reaches

  1. Asymmetric Response toward Molecular Fluorination in Binary Copper–Phthalocyanine/Pentacene Assemblies

    DEFF Research Database (Denmark)

    de Oteyza, D. G.; García Lastra, Juan Maria; Goiri, E.

    2014-01-01

    We report a didactic and simple example of the subtleness in the balance of intermolecular and molecule–substrate interactions and its effect on molecular self-assembly. The study is performed on two closely related molecular blends of copper phthalocyanines and pentacene, in each of which one...

  2. 21 CFR 73.3124 - Phthalocyanine green.

    Science.gov (United States)

    2010-04-01

    ... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3124 Phthalocyanine green. (a) Identity. The color additive is phthalocyanine green (CAS Reg. No. 1328-53-6), Colour Index No. 74260. (b) Uses... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Phthalocyanine green. 73.3124 Section 73.3124...

  3. Ambipolar Cu- and Fe-Phthalocyanine single-crystal field-effect transistors

    OpenAIRE

    de Boer, R. W. I.; Stassen, A. F.; Craciun, M. F.; Mulder, C. L.; Molinari, A; Rogge, S.; Morpurgo, A. F.

    2005-01-01

    We report the observation of ambipolar transport in field-effect transistors fabricated on single crystals of Copper- and Iron-Phthalocyanine, using gold as a high work-function metal for the fabrication of source and drain electrodes. In these devices, the room-temperature mobility of holes reaches 0.3 cm$^2$/Vs in both materials. The highest mobility for electrons is observed for Iron-Phthalocyanines and is approximately one order of magnitude lower. Our measurements indicate that these val...

  4. Theoretical study on the hydrophobic and hydrophilic hydration on large solutes: The case of phthalocyanines in water.

    Science.gov (United States)

    Martín, Elisa I; Martínez, José M; Sánchez Marcos, Enrique

    2015-07-28

    A theoretical study on the hydration phenomena of three representative Phthalocyanines (Pcs): the metal-free, H2Pc, and the metal-containing, Cu-phthalocyanine, CuPc, and its soluble sulphonated derivative, [CuPc(SO3)4](4-), is presented. Structural and dynamic properties of molecular dynamics trajectories of these Pcs in solution were evaluated. The hydration shells of the Pcs were defined by means of spheroids adapted to the solute shape. Structural analysis of the axial region compared to the peripheral region indicates that there are no significant changes among the different macrocycles, but that of [CuPc(SO3)4](4-), where the polyoxoanion presence induces a typically hydrophilic hydration structure. The analyzed water dynamic properties cover mean residence times, translational and orientational diffusion coefficients, and hydrogen bond network. These properties allow a thorough discussion about the simultaneous existence of hydrophobic and hydrophilic hydration in these macrocycles, and indicate the trend of water structure to well define shells in the environment of hydrophobic solutes. The comparison between the structural and dynamical analysis of the hydration of the amphipathic [CuPc(SO3)4](4-) and the non-soluble Cu-Pc shows a very weak coupling among the hydrophilic and hydrophobic fragments of the macrocycle. Quantitative results are employed to revisit the iceberg model proposed by Frank and Evans, leading to conclude that structure and dynamics support a non-strict interpretation of the iceberg view, although the qualitative trends pointed out by the model are supported.

  5. Synthesis and Spectroscopic Evaluation of Two Novel Glycosylated Zinc(II)-Phthalocyanines.

    Science.gov (United States)

    Bächle, Felix; Hanack, Michael; Ziegler, Thomas

    2015-10-09

    In continuation of our work on glycoconjugated phthalocyanines, two new water soluble, non-ionic zinc(II) phthalocyanines have been prepared and fully characterized by means of ¹H-NMR, 13C-NMR, MALDI-TOF, ESI-TOF, UV-Vis spectroscopy, emission spectroscopy and fluorescence lifetime measurements. The carbohydrate-containing phthalonitrile precursors were synthesized through a copper-catalyzed azide-alkyne cycloaddition (CuAAC). The 2-methoxyethoxymethyl protecting group (MEM) was used to protect the carbohydrate moieties. It resisted the harsh basic cyclotetramerization conditions and could be easily cleaved under mild acidic conditions. The glycoconjugated zinc(II) phthalocyanines described here have molar extinction coefficents εmax>10⁵ m(-1) cm(-1) and absorption maxima λ>680 nm, which make them attractive photosensitizers for photo-dynamic therapy.

  6. Synthesis and Spectroscopic Evaluation of Two Novel Glycosylated Zinc(II-Phthalocyanines

    Directory of Open Access Journals (Sweden)

    Felix Bächle

    2015-10-01

    Full Text Available In continuation of our work on glycoconjugated phthalocyanines, two new water soluble, non-ionic zinc(II phthalocyanines have been prepared and fully characterized by means of 1H-NMR, 13C-NMR, MALDI-TOF, ESI-TOF, UV-Vis spectroscopy, emission spectroscopy and fluorescence lifetime measurements. The carbohydrate-containing phthalonitrile precursors were synthesized through a copper-catalyzed azide-alkyne cycloaddition (CuAAC. The 2-methoxyethoxymethyl protecting group (MEM was used to protect the carbohydrate moieties. It resisted the harsh basic cyclotetramerization conditions and could be easily cleaved under mild acidic conditions. The glycoconjugated zinc(II phthalocyanines described here have molar extinction coefficents εmax > 105 m−1 cm−1 and absorption maxima λ > 680 nm, which make them attractive photosensitizers for photo-dynamic therapy.

  7. Organic photovoltaic cells based on unconventional electron donor fullerene and electron acceptor copper hexadecafluorophthalocyanine

    Science.gov (United States)

    Yang, J. L.; Sullivan, P.; Schumann, S.; Hancox, I.; Jones, T. S.

    2012-01-01

    We demonstrate organic discrete heterojunction photovoltaic cells based on fullerene (C60) and copper hexadecafluorophthalocyanine (F16CuPc), in which the C60 and F16CuPc act as the electron donor and the electron acceptor, respectively. The C60/F16CuPc cells fabricated with conventional and inverted architectures both exhibit comparable power conversion efficiencies. Furthermore, we show that the photocurrent in both cells is generated by a conventional exciton dissociation mechanism rather than the exciton recombination mechanism recently proposed for a similar C60/F16ZnPc system [Song et al., J. Am. Chem. Soc. 132, 4554 (2010)]. These results demonstrate that new unconventional material systems are a potential way to fabricate organic photovoltaic cells with inverted as well as conventional architectures.

  8. Phthalocyanines in batteries and supercapacitors

    CSIR Research Space (South Africa)

    Oni, J

    2012-08-01

    Full Text Available of their lower cost. This review article looks through a very narrow window of the applications of phthalocyanines in batteries and supercapacitors as a means of improving the qualities such as cycle property, energy density, capacity, open circuit voltage, etc...

  9. Distinctive contributions from organic filler and relaxorlike polymer matrix to dielectric response of CuPc-P(VDF-TrFE-CFE) composite.

    Science.gov (United States)

    Bobnar, V; Levstik, A; Huang, C; Zhang, Q M

    2004-01-30

    The dielectric response of copper-phthalocyanine (CuPc) oligomers embedded in a poly(vinylidene fluoride-trifluoroethylene-chlorofluoroethylene) terpolymer matrix was studied. Although admixture of CuPc strongly increases the dielectric constant of the terpolymer at all temperatures, each of the two constituents determines the dielectric dynamics in a different temperature region-the relaxorlike matrix above and CuPc below the terpolymer's freezing temperature. Two relaxations, reflecting the charge carriers' response in CuPc, were detected. Results on ac conductivity reveal that the tunneling of polarons is the dominating charge transport mechanism.

  10. Construction of a high efficiency copper adsorption bacterial system via peptide display and its application on copper dye polluted wastewater.

    Science.gov (United States)

    Maruthamuthu, Murali Kannan; Nadarajan, Saravanan Prabhu; Ganesh, Irisappan; Ravikumar, Sambandam; Yun, Hyungdon; Yoo, Ik-Keun; Hong, Soon Ho

    2015-11-01

    For the construction of an efficient copper waste treatment system, a cell surface display strategy was employed. The copper adsorption ability of recombinant bacterial strains displaying three different copper binding peptides were evaluated in LB Luria-Bertani medium (LB), artificial wastewater, and copper phthalocyanine containing textile dye industry wastewater samples. Structural characteristics of the three peptides were also analyzed by similarity-based structure modeling. The best binding peptide was chosen for the construction of a dimeric peptide display and the adsorption ability of the monomeric and dimeric peptide displayed strains were compared. The dimeric peptide displayed strain showed superior copper adsorption in all three tested conditions (LB, artificial wastewater, and textile dye industry wastewater). When the strains were exposed to copper phthalocyanine dye polluted wastewater, the dimeric peptide display [543.27 µmol/g DCW dry cell weight (DCW)] showed higher adsorption of copper when compared with the monomeric strains (243.53 µmol/g DCW).

  11. New metal phthalocyanines/metal simple hydroxide multilayers: experimental evidence of dipolar field-driven magnetic behavior.

    Science.gov (United States)

    Bourzami, Riadh; Eyele-Mezui, Séraphin; Delahaye, Emilie; Drillon, Marc; Rabu, Pierre; Parizel, Nathalie; Choua, Sylvie; Turek, Philippe; Rogez, Guillaume

    2014-01-21

    A series of new hybrid multilayers has been synthesized by insertion-grafting of transition metal (Cu(II), Co(II), Ni(II), and Zn(II)) tetrasulfonato phthalocyanines between layers of Cu(II) and Co(II) simple hydroxides. The structural and spectroscopic investigations confirm the formation of new layered hybrid materials in which the phthalocyanines act as pillars between the inorganic layers. The magnetic investigations show that all copper hydroxide-based compounds behave similarly, presenting an overall antiferromagnetic behavior with no ordering down to 1.8 K. On the contrary, the cobalt hydroxide-based compounds present a ferrimagnetic ordering around 6 K, regardless of the nature of the metal phthalocyanine between the inorganic layers. The latter observation points to strictly dipolar interactions between the inorganic layers. The amplitude of the dipolar field has been evaluated from X-band and Q-band EPR spectroscopy investigation (Bdipolar ≈ 30 mT).

  12. Synthesis and Properties of 1,11,15,25-Tetrahydroxy-4,8,18,22-Di (Bridged Dipropionate Carboxyl) Phthalocyanine Copper%1,11,15,25-四羟基-4,8,18,22-二(桥联二丙羧基)酞菁铜的合成及性质研究

    Institute of Scientific and Technical Information of China (English)

    夏道成; 蒲改琴; 李万程; 李洁筠; 王改萍; 段宏伟; 任旭文; 冯凯; 李佩陶; 王慧芳

    2015-01-01

    In this dissertation ,we study the synthesis and character of new substituted Phthalocyanine .Due to the widely appli‐cation of Pcs in the fields ,such as the communication ,medical treatment ,chemical industry and so on ,therefore ,they have been a hot topic over several decades by scientists .Nowadays ,scientists have prepared thousands of Pcs and their derivatives . However ,along with the human society development and the progress in science and technology ,the new phthalocyanine with novle characteristics are still the goal of the scientists .In this dissertion ,the synthetic methods of the phthlocyanine is im‐proved .The synthesis and characterization of 1 ,11 ,15 ,25‐tetrahydroxy‐4 ,8 ,18 ,22‐di(bridged dipropionate carboxyl) phthalocy‐anines are reported in this paper .The mixtures of malonic acid and 3 ,6‐dihydroxy‐phthalonitrile was added to water under stiri‐ing .Then ,a catalyst amount of sulfuric acid was added .The first synthetic precursor ,i .e .,malonic acid 3 ,3′‐bis(6‐hydroxy phthalonitrile) butter ,its molecular formula is C19 H8 N4 O6 .phthalocyanines was prepared by malonic acid 3 ,3′‐bis(6‐hydroxy phthalonitrile) butter and dihydrate zinc acetate ,copper acetate monohydrate in n‐amyl alcohol ,using DBU as a catalyst under the 135 ℃ ,molecular formula of phthalocyanine complexes is C38 H16 N8 O12 M .The product was characterized by Ultraviolet‐vis‐ible (UV/Vis) Spectrum absorption and fluorescence ,The results are agreement with the proposed structures .And electro‐chemical properties were studied .%对新型取代基酞菁和酞菁晶体合成和性质进行了研究。因为酞菁在信息、医疗、化工等众多领域有很广泛的应用,所以近百年来一直是科学家研究的热点课题。酞菁经过近百年的研究,科学家已经合成了上万种酞菁衍生物,但是,随着科技的不断进步,人类社会不断发展的需求,具有新特性的新型酞菁的获得仍

  13. An approach to conductometric immunosensor based on phthalocyanine thin film.

    Science.gov (United States)

    Sergeyeva, T A; Lavrik, N V; Rachkov, A E; Kazantseva, Z I; El'skaya, A V

    1998-03-01

    A new approach to conductometric biosensors utilizing iodine-sensitive phthalocyanine thin films has been proposed. The excellent sensitivity of the tetra-tert-butyl copper phthalocyanine (ttb-CuPc) to free iodine was used for the first time to detect a peroxidase-initiated reaction in an aqueous medium. To minimize the interfering effect of aqueous electrolytes on the impedance responses of the ttb-CuPc film itself, Au/Cr interdigitated planar electrodes bearing ttb-CuPc thin films were protected with hydrophobic gas-permeable membranes, namely thermally evaporated calixarene or plasma polymerized hexamethyldisiloxane films. Impedance spectroscopy data were analyzed in order to define the optimal operating frequency. An enzyme sensor with peroxidase immobilized in a cross-linked albumin matrix was tested. Its impedance responses were studied under variation of the substrate concentration, pH, ionic strength and buffer capacity. These results were used to define conditions for peroxidase-linked immunoassay in subsequent tests. With the developed sensor, concentrations of IgG in 0.2-2 micrograms/ml range were measured in a competitive mode with satisfactory accuracy. The detection of IgG in both test solutions and blood serum samples has been demonstrated.

  14. Laser deposition of sulfonated phthalocyanines for gas sensors

    Energy Technology Data Exchange (ETDEWEB)

    Fitl, Premysl, E-mail: fitlp@vscht.cz [Department of Physics and Measurements, Institute of Chemical Technology Prague, Technicka 5, Prague 6 CZ-166 28 (Czech Republic); Department of Analysis of Functional Materials, Institute of Physics AS CR v.v.i, Na Slovance 1999/2, Prague 8 CZ-182 21 (Czech Republic); Vrnata, Martin; Kopecky, Dusan; Vlcek, Jan; Skodova, Jitka [Department of Physics and Measurements, Institute of Chemical Technology Prague, Technicka 5, Prague 6 CZ-166 28 (Czech Republic); Bulir, Jiri; Novotny, Michal; Pokorny, Petr [Department of Analysis of Functional Materials, Institute of Physics AS CR v.v.i, Na Slovance 1999/2, Prague 8 CZ-182 21 (Czech Republic)

    2014-05-01

    Thin layers of nickel and copper tetrasulfonated phthalocyanines (NiPcTS and CuPcTS) were prepared by Matrix Assisted Pulsed Laser Evaporation method. The depositions were carried out with KrF excimer laser (energy density of laser radiation E{sub L} = 0.1–0.5 J cm{sup −2}) from dimethylsulfoxide matrix. For both materials the ablation threshold E{sub L-th} was determined. The following properties of deposited layers were characterized: (a) chemical composition (FTIR spectra); (b) morphology (SEM and AFM portraits); and (c) impedance of gas sensors based on NiPcTS and CuPcTS layers in the presence of two analytes – hydrogen and ozone. The prepared sensors exhibit response to 1000 ppm of hydrogen and 100 ppb of ozone even at laboratory temperature.

  15. Laser deposition of sulfonated phthalocyanines for gas sensors

    Science.gov (United States)

    Fitl, Premysl; Vrnata, Martin; Kopecky, Dusan; Vlcek, Jan; Skodova, Jitka; Bulir, Jiri; Novotny, Michal; Pokorny, Petr

    2014-05-01

    Thin layers of nickel and copper tetrasulfonated phthalocyanines (NiPcTS and CuPcTS) were prepared by Matrix Assisted Pulsed Laser Evaporation method. The depositions were carried out with KrF excimer laser (energy density of laser radiation EL = 0.1-0.5 J cm-2) from dimethylsulfoxide matrix. For both materials the ablation threshold EL-th was determined. The following properties of deposited layers were characterized: (a) chemical composition (FTIR spectra); (b) morphology (SEM and AFM portraits); and (c) impedance of gas sensors based on NiPcTS and CuPcTS layers in the presence of two analytes - hydrogen and ozone. The prepared sensors exhibit response to 1000 ppm of hydrogen and 100 ppb of ozone even at laboratory temperature.

  16. 用溶胶-凝胶法制备铜酞菁固体材料及其光学性质%FABRICATION OF SOLID STATE MATERIALS CONTAINING COPPER- PHTHALOCYANINE BY SOL-GEL METHOD AND THEIR OPTICAL PROPERTIES

    Institute of Scientific and Technical Information of China (English)

    夏海平; 章践立; 张约品; 聂秋华

    2001-01-01

    运用溶胶-凝胶技术,利用γ-氨基丙基三乙氧基硅烷( 3-aminopropyltriethoxysilane, NH2 ( CH2)3Si( OC2H5 )3, KH550 )中氨基与4-羧基铜酞菁[ (Tetracarboxyphalocyaninato)copper( Ⅱ ), CuPc(COOH)4]中羧基的化学作用,成功地把CuPc(COOH)4以较大浓度均匀地掺入到KH550与γ-缩水甘油醚基丙基三甲氧基硅烷(3-glycidoxypropl-trimethoxysilane,CH2OCHCH2O(CH2)3Si(OCH3)3,KH560)为先驱体的凝胶介质中。红外光谱表征了CuPc(COOH)4与KH550的化学反应过程。用波长为532nm,脉宽8ns的Nd3+:YAG激光对复合材料的光限幅特征作了初步的研究。%(Tetracarboxyphalocyaninato) copper (II) was incorporated in gel with a high concentration by a sol-gel process using 3-aminopropyltriethoxysilane(NH2 ( CH2)3Si( OC2H5)3, KH550) and 3 - glycidoxy- propltrimethoxysiolane ( CH2OCHCH2O( CH2)3Si (OCH3)3,KH550) as precursors due to the chemical reaction between NH2 group of KH550 and COOH group of CuPc(COOH)4.The linkage of CuPc(COOH)4 and KH550 was estimated by FT- IR spectra, and the primary optical limiting effect of the solid state material was studied with the use of 8 ns, 532 nm laser pulse.

  17. Nanofabrication of organic/inorganic hybrids of TiO2 with substituted phthalocyanine or polythiophene.

    Science.gov (United States)

    Ding, H; Ram, M K; Nicolini, C

    2001-06-01

    Organic photovoltaic cells, similar to Grätzel type, have been widely investigated in recent years. In the case of Grätzel-type cells, TiO2 colloids are usually spin-coated onto an electrode and then sintered. Later, such electrodes are immersed in dye solution to sensitize the TiO2 layer for fabrication of photovoltaic cells. In the current study, an attempt was made to fabricate photovoltaic cells using a layer-by-layer technique. Based on such a method, ordered substituted phthalocyanine or conducting polythiophene-sensitized TiO2 multilayers were fabricated at the molecular level. Buildup of multilayer films of copper phthalocyanine-capped TiO2 and poly(thiophene-3-acetic acid)/TiO2 was monitored by increments in the UV-visible absorption and the frequency decrease of quartz crystal microbalance. The ordered multilayers were further characterized by infrared spectroscopy, and electrochemical and photoelectrochemical measurements.

  18. Three new phthalocyanines with potential for PDT studies

    Science.gov (United States)

    Rihter, Boris D.; Bohorquez, Maria D.; Rodgers, Michael A. J.; Kenney, Malcolm E.

    1992-06-01

    The synthesis and characterization of a tetradibenzobarrelenoocta-n-butoxyzinc phthalocyanine, as well as the phthalocyanines t-butyldimethylsiloxy-N(3(beta) -acetoxy-23, 24-dinor-5-cholenoyl)-4-amino-n-butyldimethylsiloxysilicon phthalocyanine and bis- N(3(beta) -acetoxy-23,24-dinor-5-cholenoyl)-4-amino-n-butyldimethylsiloxysilicon phthalocyanine are reported. The zinc phthalocyanine is soluble, open at its center and highly hindered. It has a deep red absorption and a long triplet state lifetime. The silicon phthalocyanines have red absorptions and ligands bearing functions that have a resemblance to a part of the core of the low density lipoprotein fraction of blood serum. The zinc phthalocyanine has the potential to be a good photosensitizer, and the silicon phthalocyanines or related compounds have the potential to be preferentially accumulated by tumor cells. All three compounds are of interest for photodynamic therapy studies.

  19. Photochemical studies and nanomolar photodynamic activities of phthalocyanines functionalized with 1,4,7-trioxanonyl moieties at their non-peripheral positions.

    Science.gov (United States)

    Sobotta, Lukasz; Wierzchowski, Marcin; Mierzwicki, Michal; Gdaniec, Zofia; Mielcarek, Jadwiga; Persoons, Leentje; Goslinski, Tomasz; Balzarini, Jan

    2016-02-01

    Manganese(III), cobalt(II), copper(II), magnesium(II), zinc(II) and metal-free phthalocyanines, possessing 1,4,7-trioxanonyl substituents, at their non-peripheral positions, were subjected to photochemical, photodynamic and biological activity studies. Demetallated phthalocyanine and its metallated d-block analogues, with copper(II), cobalt(II), manganese(III) chloride, were found to be less efficient singlet oxygen generators in comparison to the zinc(II) analogue and zinc(II) phthalocyanine reference. Irradiation of several phthalocyanines for short time periods resulted in a substantially increased cytostatic activity against both suspension (leukemic/lymphoma at 85nM) and solid (cervix carcinoma at 72nM and melanoma at 81nM) tumour cell lines (up to 200-fold). Noteworthy is that enveloped viruses, such as for herpesvirus and influenza A virus, but not, non-enveloped virus strains, such as Coxsackie B4 virus and reovirus-1, exposed to irradiation in the presence of the phthalocyanines, markedly lost their infectivity potential. Copyright © 2015 Elsevier Inc. All rights reserved.

  20. An ab-initio density functional theory investigation of fullerene/Zn-phthalocyanine (C60/ZnPc) interface with face-on orientation

    Energy Technology Data Exchange (ETDEWEB)

    Javaid, Saqib [EMMG, Physics Division, PINSTECH, P.O. Nilore, Islamabad (Pakistan); National Centre of Physics, Islamabad (Pakistan); Javed Akhtar, M., E-mail: javedakhtar6@gmail.com [EMMG, Physics Division, PINSTECH, P.O. Nilore, Islamabad (Pakistan)

    2015-07-28

    We have employed density functional theory to study the C60/ZnPc interface with face-on orientation, which has recently been tailored experimentally. For this purpose, adsorption of ZnPc on C60 has been studied, while taking into account different orientations of C60. Out of various adsorption sites investigated, 6:6 C-C bridge position in apex configuration of C60 has been found energetically the most favourable one with C60-ZnPc adsorption distance of ∼2.77 Å. The adsorption of ZnPc on C60 ensues both charge re-organization and charge transfer at the interface, resulting in the formation of interface dipole. Moreover, by comparing results with that of C60/CuPc interface, we show that the direction of interface dipole can be tuned by the change of the central atom of the phthalocyanine molecule. These results highlight the complexity of electronic interactions present at the C60/Phthalocyanine interface.

  1. Covalently Linked Dyads and Triads of Phthalocyanines and Porphyrins

    OpenAIRE

    Aljuhani, Ateyat Allah

    2014-01-01

    The phthalocyanines are a family of intensively coloured compounds, with some important properties and are classified as important materials for many applications. Structurally, a phthalocyanine is similar to a porphyrin. In chapter one, a brief introduction of their synthesis, properties, and applications is given along with some examples of phthalocyanine dimers. The preparation of new functionalised phthalocyanine and porphyrin compounds has been the subject of intense research over the la...

  2. Studies of phthalocyanine-containing polymers

    Science.gov (United States)

    Lee, Pui Sze Priscilla

    This thesis reports the synthesis, spectroscopic and photophysical properties, and in vitro photodynamic activities of several series of phthalocyanine-containing polymers including poly(norbornene), poly(anhydride), and poly(epsilon-caprolactone). Chapter 1 gives a general overview of phthalocyanines including their synthesis and applications. Special emphasis has been placed on hydrophilic and non-aggregated phthalocyanines and their use in photodynamic therapy. In addition, different classes of phthalocyanine-containing polymers will also be mentioned. Chapter 2 discusses the synthesis, characterization, and photophysical properties of a series of poly(norbornene)s with zinc(II) phthalocyanine and amino acid moieties. The copolymers were prepared by copolymerization of 2-(2-norbornenylmethoxy)phthalocyaninatozinc(II) with 5-norbornenes substituted with phenylalanine and tyrosine. As shown by absorption and fluorescence spectroscopy, phthalocyanines in this series of polymer exhibit a rather strong aggregation tendency. Chapter 3 presents the synthesis, characterization, photophysical properties, and in vitro photodynamic activities of a related series of amino acid- and sugar-containing poly(norbornene)s connected axially to a silicon(IV) phthalocyanine core. These polymers exhibit a good solubility in common organic solvents. Due to the axial polymeric substituents, these compounds are free from aggregation and give a high singlet oxygen quantum yield. These polymers in Cremophor EL emulsions also show a high photodynamic activity against HepG2 cells, in particular the polymer with protected galactose moieties. Chapter 4 reports a series of silicon(IV) phthalocyanines substituted with two poly(sebacic anhydride) chains as the axial ligands. The polymers form nanoparticles in water in the presence of surfactants cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulphate (SDS). The degradation of the nanoparticles was carried out in alkaline media and was

  3. Syntheses and Functional Properties of Phthalocyanines

    Directory of Open Access Journals (Sweden)

    Keiichi Sakamoto

    2009-08-01

    Full Text Available Metal phthalocyanine tetrasulfonic acids, metal phthalocyanine octacarboxylic acids, metal octakis(hexyloxymethylphthalocyanines, and metal anthraquinocyanines have been synthesized. Then, zinc bis(1,4-didecylbenzo-bis(3,4-pyridoporphyrazines, the cyclotetramerization products of a 1:1 mixture of 3,6-didecylphthalonitrile and 3,4-dicyanopyridine, were synthesized. Futher, subphthalocyanine and its derivatives, with substituents such as thiobutyl and thiophenyl moieties were synthesized. Electrochemical measurements were performed on the abovementioned phthalocyanine derivatives and analogues in order to examine their electron transfer abilities and electrochemical reaction mechanisms in an organic solvent. Moreover, 1,4,8,11,15,18,22,25-octakis(thiophenylmethyl phthalocyanes were synthesized. The Q-bands of the latter compounds appeared in the near-infrared region. Furthermore, non-colored transparent films in the visible region can be produced.

  4. An Electrochemical Quartz Crystal Microbalance Multisensor System Based on Phthalocyanine Nanostructured Films: Discrimination of Musts

    Directory of Open Access Journals (Sweden)

    Celia Garcia-Hernandez

    2015-11-01

    Full Text Available An array of electrochemical quartz crystal electrodes (EQCM modified with nanostructured films based on phthalocyanines was developed and used to discriminate musts prepared from different varieties of grapes. Nanostructured films of iron, nickel and copper phthalocyanines were deposited on Pt/quartz crystals through the Layer by Layer technique by alternating layers of the corresponding phthalocyanine and poly-allylamine hydrochloride. Simultaneous electrochemical and mass measurements were used to study the mass changes accompanying the oxidation of electroactive species present in must samples obtained from six Spanish varieties of grapes (Juan García, Prieto Picudo, Mencía Regadío, Cabernet Sauvignon, Garnacha and Tempranillo. The mass and voltammetric outputs were processed using three-way models. Parallel Factor Analysis (PARAFAC was successfully used to discriminate the must samples according to their variety. Multi-way partial least squares (N-PLS evidenced the correlations existing between the voltammetric data and the polyphenolic content measured by chemical methods. Similarly, N-PLS showed a correlation between mass outputs and parameters related to the sugar content. These results demonstrated that electronic tongues based on arrays of EQCM sensors can offer advantages over arrays of mass or voltammetric sensors used separately.

  5. Charge transport properties of metal/metal-phthalocyanine/n-Si structures

    Energy Technology Data Exchange (ETDEWEB)

    Hussain, Afzal

    2010-12-16

    In present work the charge transport properties of metal/metal-phthalocyanine/n-Si structures with low (N{sub D} = 4 x 10{sup 14} cm{sup -3}), medium (N{sub D}=1 x 10{sup 16} cm{sup -3}) and high (N{sub D}=2 x 10{sup 19} cm{sup -3}) doped n-Si as injecting electrode and the effect of air exposure of the vacuum evaporated metal-phthalocyanine film in these structures is investigated. The results obtained through temperature dependent electrical characterizations of the structures suggest that in terms of dominant conduction mechanism in the corresponding devices Schottky-type conduction mechanism dominates the charge transport in low-bias region of these devices up to 0.8 V, 0.302 V and 0.15 V in case of low, medium and high doped n-Silicon devices. For higher voltages, in each case of devices, the space-charge-limited conduction, controlled by exponential trap distribution, is found to dominate the charge transport properties of the devices. The interface density of states at the CuPc/n-Si interface of the devices are found to be lower in case of lower work function difference at the CuPc/n-Si interface of the devices. The results also suggest that the work function difference at the CuPc/n-Si interface of these devices causes charge transfer at the interface and these phenomena results in formation of interface dipole. The width of the Schottky depletion region at the CuPc/n-Si interface of these devices is found to be higher with higher work function difference at the interface. The investigation of charge transport properties of Al/ZnPc/medium n-Si and Au/ZnPc/ medium n-Si devices suggest that the Schottky depletion region formed at the ZnPc/n-Si interface of these devices determines the charge transport in the low-bias region of both the devices. Therefore, the Schottky-type (injection limited) and the space-charge-limited (bulk limited) conduction are observed in the low and the high bias regions of these devices, respectively. The determined width of the

  6. Submonolayer and multilayer growth of titaniumoxide-phthalocyanine on Ag(111)

    Science.gov (United States)

    Kröger, Ingo; Stadtmüller, Benjamin; Kumpf, Christian

    2016-11-01

    For exploiting the full potential of organic materials for future organic electronic devices it is of crucial importance to understand structural and electronic properties of metal-organic interfaces and adsorbate systems, in particular electronic interactions and growth mechanisms. Phthalocyanine molecules represent one class of materials which are very frequently discussed in this context. They feature an appealing tunability in terms of structural, electronic and magnetic properties, simply by exchanging the central (metal) atom or group of atoms. Here we present a comprehensive study of one of the model systems in this field, TiOPc on Ag(111). We discuss structure formation and growth from submonolayer to multilayer films, based on results obtained by electron diffraction, scanning tunneling microscopy, electron energy loss spectroscopy, x-ray standing waves, photoelectron spectroscopy and pair potential calculations. Similar to related metal-phthalocyanine adsorbate systems we find three distinct phases in the submonolayer regime, a disordered gas-like ‘g-phase’, a commensurate ‘c2-phase’ at low temperature, and a ‘p.o.l.-phase’ consisting of a series of point-on-line structures with continuously shrinking unit cells. For the latter a uniform TiO-up configuration (Ti-O group pointing towards vacuum) was found. Hence, the first-layer molecules form a strong dipole layer, the dipole moment of which is compensated by molecules adsorbing in the second layer at hollow-sites in TiO-down geometry (Ti-O group pointing towards the surface). The Coulomb interaction between the dipole moments in the first and second layer stabilizes this bilayer structure and causes a bilayer-by-bilayer growth mode of molecular films above a thickness of 2 ML. We report the structural properties (vertical adsorption heights, inter-layer distances, inplane orientations and positions) of the molecules in all phases in detail, and discuss the effect of inelastic dynamical charge

  7. Langmuir Blodgett films of porphyrins and phthalocyanines

    CERN Document Server

    Portus, D

    2002-01-01

    Phthalocyanines and porphyrins have been studied for many years as bulk, thick and thin films. Their use in Langmuir and Langmuir-Blodgett films is governed by their peripheral substituents. These can enhance or reduce their ability to form 'quality' ultra-thin films. There are a number of potential and current applications for thin films of porphyrins and phthalocyanines, which include CD-R discs and gas-sensors. It is the latter that this PhD has focussed on. Ultra-thin films of phthalocyanines, porphyrins and a porphyrin/phthalocyanine hybrid dye were deposited onto glass microscope slides, gold-coated glass microscope slides and quartz crystals. These assemblies were then characterised using Ultraviolet-Visible spectroscopy, pressure-area isotherms, surface plasmon resonance and a quartz crystal microbalance to try and determine the nature of the molecules on the surface of the substrate. The thin films were exposed to chlorine gas and the change in their absorption spectrum and (in some cases) their surf...

  8. [Photophysical properties and photodynamic activity of nanostructured aluminium phthalocyanines].

    Science.gov (United States)

    Udartseva, O O; Lobanov, A V; Andeeva, E R; Dmitrieva, G S; Mel'nikov, M Ia; Buravkova, L B

    2014-01-01

    We developed water-soluble supramolecular complexes of aluminium phthalocyanine based on mesoporous silica nanoparticles and polyvinylpirrolidone containing rare photoactive nanoaggregates. Radiative lifetimes, extinction coefficients and energy of electronic transitions of isolated and associated metal phthalocyanine complexes were calculated. Nontoxic concentrations of synthesized nanocomposite photosensibilizers were in vitro determined. In present study we compared photodynamic treatment efficacy using different modifications of aluminium phthalocyanine (Photosens®, AlPc-nSiO2 and AlPc-PVP). Mesenchymal stromal cells were used as a model for photodynamic treatment. Intracellular accumulation of aluminium phthalocyanine based on mesoporous silica nanoparticles AlPc-nSiO2 was the most efficient. Illumination of phthalocyanine-loaded cells led to reactive oxygen species generation and subsequent apoptotic cell death. Silica nanoparticles provided a significant decrease of effective phthalocyanine concentration and enhanced cytotoxicity of photodynamic treatment.

  9. Structure-Stability Relationships of Phthalocyanine Copper Complexes

    Directory of Open Access Journals (Sweden)

    G. P. Shaposhnikov

    2000-06-01

    Full Text Available The influence of NO2, Br, and COOH function substituents in various positions of Cu(IIPc on the reactivity of the latter concerning the dissociation of the metal - nitrogen bonds in proton donor solvents is discussed.

  10. Near room temperature ferromagnetism of copper phthalocyanine thin films

    Energy Technology Data Exchange (ETDEWEB)

    Wang, XueYan, E-mail: xueyanadeline@163.com; Zheng, JianBang; Chen, Lei; Qiao, Kai; Xu, JiaWei; Cao, ChongDe

    2015-11-30

    Highlights: • The α-CuPc films without and with light Ni-doping were characterized by X-ray photoelectron spectroscopy to confirm the absence of other ferromagnetic impurities. • The α-CuPc film exhibited ferromagnetic hysteresis with saturation magnetization of ∼6.77 emu/cm{sup 3} and coercivity of ∼96 Oe at 280 K, while that of the Ni-doped α-CuPc film are ∼0.69 emu/cm{sup 3} and ∼113 Oe, respectively. • Through the density functional theory calculations, the origin of the ferromagnetism arise from Cu 3d states and N 2s2p electronic spin polarization, as well as p–d exchange coupling interactions, and spin-unbalanced electronic structure of C 2p induced by the π–π interactions. - Abstract: We reported near room temperature ferromagnetism of α-CuPc films without and with light Ni-doping. Two samples were characterized by X-ray photoelectron spectroscopy (XPS) to confirm the absence of other ferromagnetic impurities. The α-CuPc film exhibited ferromagnetic hysteresis with saturation magnetization of ∼6.77 emu/cm{sup 3} and coercivity of ∼96 Oe at 280 K, while that of the Ni-doped α-CuPc film are ∼0.69 emu/cm{sup 3} and ∼113 Oe, respectively. Through the density functional theory (DFT) calculations, the origin of the ferromagnetism arise from Cu 3d states and N 2s2p electronic spin polarization, as well as p-d exchange coupling interactions, and spin-unbalanced electronic structure of C 2p induced by the π–π interactions.

  11. Crystal fields of porphyrins and phthalocyanines

    Science.gov (United States)

    Johnson, P. S.; Boukahil, I.; Himpsel, F. J.; Kennedy, C.; Jersett, N.; Cook, P. L.; Garcia-Lastra, J. M.

    2014-03-01

    Polarization-dependent X-ray absorption spectroscopy at the N 1s and metal 2p edges is combined with density functional and atomic multiplet calculations to determine the crystal field parameters 10Dq, Ds, and Dt of transition metal (Mn, Fe, Co, Ni) phthalocyanines and octaethylporphyrins. Octaethyl porphyrins are observed to lie flat on Si with native oxide, while phthalocyanines lie on edge. Strong polarization dependence is found at all edges, which facilitates a unique determination of the crystal field parameters. Crystal field values from PBE density functional calculations provide helpful starting values, which are refined by fitting atomic multiplet calculations to the data. Since the crystal field affects electron-hole separation in solar cells, the systematic set of crystal field parameters obtained here can be useful for optimizing dyes for solar cells.

  12. Perfluorinated cobalt phthalocyanine effectively catalyzes water electrooxidation

    KAUST Repository

    Morlanes, Natalia Sanchez

    2014-12-08

    Efficient electrocatalysis of water oxidation under mild conditions at neutral pH was achieved by a fluorinated cobalt phthalocyanine immobilized on fluorine-doped tin oxide (FTO) surfaces with an onset potential at 1.7 V vs. RHE. Spectroscopic, electrochemical, and inhibition studies indicate that phthalocyanine molecular species are the operational active sites. Neither free cobalt ions nor heterogeneous cobalt oxide particles or films were observed. During long-term controlled-potential electrolysis at 2 V vs. RHE (phosphate buffer, pH 7), electrocatalytic water oxidation was sustained for at least 8 h (TON ≈ 1.0 × 105), producing about 4 μmol O2 h-1 cm-2 with a turnover frequency (TOF) of about 3.6 s-1 and no measurable catalyst degradation.

  13. Photophysics of silicon phthalocyanines in aqueous media.

    Science.gov (United States)

    Doane, Tennyson L; Chuang, Chi-Hung; Chomas, Andrew; Burda, Clemens

    2013-02-04

    Phthalocyanines have been used as photodynamic therapy (PDT) agents because of their uniquely favorable optical properties and high photostability. They have been shown to be highly successful for the treatment of cancer through efficient singlet-oxygen ((1)O(2)) production. However, due to their hydrophobic properties, the considerations of solubility and cellular location have made understanding their photophysics in vitro and in vivo difficult. Indeed, many quantitative assessments of PDT reagents are undertaken in purely organic solvents, presenting challenges for interpreting observations during practical application in vivo. With steady-state and time-resolved laser spectroscopy, we show that for axial ligated silicon phthalocyanines in aqueous media, both the water:lipophile ratio and the pH have drastic effects on their photophysics, and ultimately dictate their functionality as PDT drugs. We suggest that considering the presented photophysics for PDT drugs in aqueous solutions leads to guidelines for a next generation of even more potent PDT agents.

  14. Porphyrins and phthalocyanines in solar photovoltaic cells

    OpenAIRE

    Walter, Michael G.; Rudine, Alexander B.; Wamser, Carl C.

    2010-01-01

    This review summarizes recent advances in the use of porphyrins, phthalocyanines, and related compounds as components of solar cells, including organic molecular solar cells, polymer cells, and dye-sensitized solar cells. The recent report of a porphyrin dye that achieves 11% power conversion efficiency in a dye-sensitized solar cell indicates that these classes of compounds can be as efficient as the more commonly used ruthenium bipyridyl derivatives.

  15. Lighting porphyrins and phthalocyanines for molecular photovoltaics.

    Science.gov (United States)

    Martínez-Díaz, M Victoria; de la Torre, Gema; Torres, Tomás

    2010-10-14

    The field of organic photovoltaics (OPV) represents one of the most promising technological areas. Porphyrins and phthalocyanines are perfectly suited for their integration in light energy conversion systems. These colored macrocycles exhibit very attractive physical properties, particularly very high extinction coefficients in the visible and near IR regions, where the maximum of the solar photon flux occurs, that is necessary for efficient photon harvesting, besides a rich redox chemistry, as well as photoinduced electron transfer and semiconducting capabilities.

  16. Substitution of phthalocyanines affecting the properties of their films and heterostructures

    Science.gov (United States)

    Vertsimakha, Ya.; Mamykin, S.; Lutsyk, P.

    2012-08-01

    Optical and photovoltaic properties were studied for phthalocyanine derivatives: sulfonamide zinc phthalocyanine (ZPS), amine zinc phthalocyanine (ZPN) and amine metal-free phthalocyanine (HPN) thin films and thin-film heterostructures made of the phthalocyanine derivatives with organic semiconductors - N,N‧-dimethylperylene-tetracarboxylicacid diimide, pentacene, lead phthalocyanine. It was shown that sulphonamide substitution of phthalocyanine molecule practically does not affect the absorption spectra. NH2 substitution results in appearance of additional absorbance in long-wave range in comparison to the spectra of ZPS. The behavior can be explained by an increase of molecular aggregation due to more efficient interaction of NH2 substituted phthalocyanines. The photovoltaic sensitivity of the phthalocyanine films decreases in following sequence ZPS → ZPN → HPN. Thermal deposition of N,N‧-dimethylperylene-tetracarboxylicacid diimide and pentacene on thin films of the phthalocyanine derivatives results in formation of sufficiently high potential barrier at the interface. The highest photosensitivity was observed in the heterostructures with pentacene films.

  17. An ultrafast study of Zinc Phthalocyanine in DMSO

    CSIR Research Space (South Africa)

    Ombinda-Lemboumba, Saturnin

    2010-10-01

    Full Text Available The ultrafast dynamics of Zinc Phthalocyanine was studied using trasient absorption pump probe spectroscopy. Zinc Phthalocyanine was excited (pumped) at 672nm and probed by a white light continuum. The pump-probe technique used in this study...

  18. Photoinduced electron transfer between benzyloxy dendrimer phthalocyanine and benzoquinone

    Science.gov (United States)

    Zhang, Tiantian; Ma, Dongdong; Pan, Sujuan; Wu, Shijun; Jiang, Yufeng; Zeng, Di; Yang, Hongqin; Peng, Yiru

    2016-10-01

    Photo-induced electron transfer (PET) is an important and fundamental process in natural photosynthesis. To mimic such interesting PET process, a suitable donor and acceptor couple were properly chosen. Dendrimer phthalocyanines and their derivatives have emerged as promising materials for artificial photosynthesis systems. In this paper, the electron transfer between the light harvest dendrimer phthalocyanine (donor) and the 1,4-benzoquinone (acceptor) was studied by UV/Vis and fluorescence spectroscopic methods. It was found that fluorescence of phthalocyanine was quenched by benzoquinone (BQ) via excited state electron transfer, from the phthalocyanine to the BQ upon excitation at 610 nm. The Stern-Volmer constant (KSV) of electron transfer was calculated. Our study suggests that this dendritic phthalocyanine is an effective new electron donor and transmission complex and could be used as a potential artificial photosynthesis system.

  19. One step grafting of iron phthalocyanine containing flexible chains on Fe{sub 3}O{sub 4} nanoparticles towards high performance polymer magnetic composites

    Energy Technology Data Exchange (ETDEWEB)

    Pu, Zejun; Zhou, Xuefei; Yang, Xulin; Jia, Kun, E-mail: Jiakun@uestc.edu.cn; Liu, Xiaobo, E-mail: liuxb@uestc.edu.cn

    2015-07-01

    To develop high-performance inorganic particles/polymer composites, the interfacial interaction and dispersion of inorganic particles are the two essential issues to be considered. Herein, we report an effective approach to graft iron phthalocyanine containing flexible chains (NP-ph) on Fe{sub 3}O{sub 4} nanoparticles (NP-ph@Fe{sub 3}O{sub 4}). The hybrids were monodispersed solid nanoparticles with the average diameter of about 250 nm. About 16.8% of the phthalocyanine oligomer was incorporated into the resulting NP-ph@Fe{sub 3}O{sub 4} nanoparticles. The NP-ph@Fe{sub 3}O{sub 4} nanoparticles were subsequently used as the novel filler for preparation of high performance poly(arylene ether nitrile)s (PAEN) composites. The scanning electron microscopy (SEM) investigation showed that the NP-ph@Fe{sub 3}O{sub 4} nanoparticles present better dispersion and interfacial compatibility with PAEN matrix than that of raw Fe{sub 3}O{sub 4}, which was further confirmed by rheological study. Consequently, the improved thermal stability and enhanced mechanical properties were obtained from composites using NP-ph@Fe{sub 3}O{sub 4}. Vibrating sample magnetometer (VSM) results showed that the prepared PAEN composites exhibited higher saturation magnetization and soft magnetic properties. Meanwhile, the saturation magnetization (Ms) of the PAEN/NP-ph@Fe{sub 3}O{sub 4} composite films increased with the increase of the hybrid nanoparticles loading. Thus, the PAEN/NP-ph@Fe{sub 3}O{sub 4} composite would find potential applications in organic magnetic films fields due to their high thermal stability, excellent flexibility and tunable magnetic properties. - Highlights: • An effective approach to graft CuPc containing flexible chains on Fe. • Effect on the mechanical, thermal and interfacial properties were investigated. • The dispersion state was characterized using parallel-plate rheometry. • The mechanism of interfacial compatibility was clarified.

  20. Surface asperity evolution and microstructure analysis of Al 6061T5 alloy in a quasi-static cold uniaxial planar compression (CUPC)

    Energy Technology Data Exchange (ETDEWEB)

    Li, Hejie, E-mail: hejiel2003@gmail.com [School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, Wollongong, NSW 2522 (Australia); Jiang, Zhengyi, E-mail: jiang@uow.edu.au [School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, Wollongong, NSW 2522 (Australia); Wei, Dongbin [School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, Wollongong, NSW 2522 (Australia); School of Electrical, Mechanical and Mechatronic Systems, University of Technology, Sydney, NSW 2007 (Australia); Gao, Xingjian [School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, Wollongong, NSW 2522 (Australia); Xu, Jianzhong; Zhang, Xiaoming [State Key Laboratory of Rolling and Automation, Northeastern University, Shenyang, Liaoning 110004 (China)

    2015-08-30

    Highlights: • We used AFM and EBSD to analyses the surface asperity flattening process. • Analysis of the influence of deformation rate on the surface asperity flattening. • Investigation of the effect of lubrication on microstructure development. • Deformation rate influence the generation of orientation components obviously. - Abstract: In a quasi-static cold uniaxial planar compression, surface asperity evolution and microstructure analysis of Al 6061T5 alloy are carried out by employing Atomic Force Microscope (AFM) and Electron Backscattered Diffraction (EBSD) methods. Strain rate affects the surface asperity evolution obviously. While lubrication can hinder the surface asperity flattening by constraining the surface localized deformation. Lubrication can accelerate the crystallization in CUPC process. It also impedes the activation of some orientation components by hindering the activation of related slip systems in light metal Al alloy.

  1. Resonance Raman spectra of phthalocyanine monolayers on different supports. A normal mode analysis of zinc phthalocyanine by means of the MNDO method

    NARCIS (Netherlands)

    Palys, Barbara J.; Ham, van den Dirk M.W.; Briels, Wim; Feil, Dirk

    1995-01-01

    Resonance Raman spectra of monolayers of transition metal phthalocyanines reveal specific interaction with the support. To elucidate its mechanism, Raman spectra of zinc phthalocyanine monolayers were studied. The analysis was based largely on the results of MNDO calculations. Calculated wavenumbers

  2. Resonance Raman spectra of phthalocyanine monolayers on different supports. A normal mode analysis of zinc phthalocyanine by means of the MNDO method

    NARCIS (Netherlands)

    Palys, Barbara J.; van den Ham, Dirk M.W.; van den Ham, D.M.W.; Briels, Willem J.; Feil, D.; Feil, Dirk

    1995-01-01

    Resonance Raman spectra of monolayers of transition metal phthalocyanines reveal specific interaction with the support. To elucidate its mechanism, Raman spectra of zinc phthalocyanine monolayers were studied. The analysis was based largely on the results of MNDO calculations. Calculated wavenumbers

  3. Controlling Growth Orientation of Phthalocyanine Films by Electrical Fields

    Science.gov (United States)

    Zhu, S.; Banks, C. E.; Frazier, D. O.; Ila, D.; Muntele, I.; Penn, B. G.; Sharma, A.; Rose, M. Franklin (Technical Monitor)

    2001-01-01

    Organic Phthalocyanine films have many applications ranging from data storage to various non-linear optical devices whose quality is affected by the growth orientation of Phthalocyanine films. Due to the structural and electrical properties of Phthalocyanine molecules, the film growth orientation depends strongly on the substrate surface states. In this presentation, an electrical field up to 4000 V/cm is introduced during film growth. The Phthalocyanine films are synthesized on quartz substrates using thermal evaporation. An intermediate layer is deposited on some substrates for introducing the electrical field. Scanning electron microscopy, x-ray diffraction, and Fourier transform infrared spectroscopy are used for measuring surface morphology, film structure, and optical properties, respectively. The comparison of Phthalocyanine films grown with and without the electrical field reveals different morphology, film density, and growth orientation, which eventually change optical properties of these films. These results suggest that the growth method in the electrical field can be used to synthesized Phthalocyanine films with a preferred crystal orientation as well as propose an interaction mechanism between the substrate surface and the depositing molecules. The details of growth conditions and of the growth model of how the Phthalocyanine molecules grow in the electrical field will be discussed.

  4. The photochemical properties of fluoroaluminum phthalocyanine.

    Science.gov (United States)

    Rosenthal, I; Shafirovich, V Y; Geacintov, N E; Ben-Hur, E; Horowitz, B

    1994-09-01

    Fluoride is known to inhibit the photodynamic activity of aluminium phthalocyanine in a variety of biological systems. In order to gain insight into this phenomenon, the effect of fluoride on the photophysical properties of free and albumin-bound chloroaluminum phthalocyanine sulfonate (AlPcSn) were studied. The association constant of NaF with AlPcSn in aqueous solution was measured as 500 +/- 20 M-1. This binding affects the photophysical properties of the dye: the absorption bands in the visible range are blue-shifted by 6-8 nm, and this effect is mirrored in the fluorescence emission spectrum. Human serum albumin significantly quenched the dye fluorescence independent of the presence of fluoride ion. The transient absorption spectrum of the excited dye triplet is unchanged by NaF, but the quantum yield for its generation is increased by 50%, with no decrease in its lifetime. Formation of fluoroaluminum phthalocyanine complexes was also observed in tetrabutylammonium fluoride-assisted solutions in wet acetonitrile. The fluoro-AlPcSn complex is a better photosensitizer for generation of singlet oxygen than the original dye-hydroxyl ion complex, as confirmed using the imidazole-N,N-dimethyl-4-nitrosoaniline method. On the other hand, the fluoro-AlPcSn complex exhibits an intense inhibitory effect on photohemolysis of red blood cells (RBC) even after the cells are washed to remove free dye and fluoride prior to irradiation, indicating that once the dye is attached to the cellular site, the fluoride ligand is no longer prone to displacement (by hydroxyl ion, for example). Nonetheless, it is clear from the spectroscopic data that the new fluoro complex is an efficient sensitizer for photooxidation.(ABSTRACT TRUNCATED AT 250 WORDS)

  5. Side chain polysiloxanes with phthalocyanine moieties

    Directory of Open Access Journals (Sweden)

    T. Ganicz

    2012-05-01

    Full Text Available Side chain polysiloxane with 5-(pentyloxy-3-methyloxy-9,10,16,17,23,24-hexakis(octenyloxyphthalocyanine moieties is synthesized by hydrosilylation reaction. The phase behavior and thermooptical properties of the polysiloxane and starting 2-(pent-4-enyloxy-3-methyloxy-9,10,16,17,23,24-hexakis(octenyloxyphthalocyanine is examined by POM (Polarizing optical microscopy, TOA (thermooptical analysis, DSC (differential scanning calorimetry, AFM (atomic force microscopy and SAXS (small angle X-ray scattering studies. The effect of the attachment of phthalocyanine to polysiloxane chains over phase transitions and phase morphology is discussed in details.

  6. Intrinsic Semiconducting Materials on Phthalocyanine Basis

    OpenAIRE

    Hanack, Michael

    2014-01-01

    Stacked transition metal macrocycles [MacM(L)]n with M e.g. Fe, Ru, Os, Co, Rh and Mac = phthalocyanine (Pc) 1,2- or 2,3-naphthalocyanine (1,2-, 2,3-Nc) were synthesized. The bridging ligands (L) may be e.g. pyrazine (pyz) or s-tetrazine (tz). In general, these complexes [MacM(L)]n are insoluble in organic solvents; however, soluble oligomers [R4PcM(L)]n can be prepared using metallomacrocycles RnPcM, R = t-bu, et, OR, M = Fe, Ru, which are substituted in the peripheric positions. A systemati...

  7. Formation of highly toxic hydrogen cyanide upon ruby laser irradiation of the tattoo pigment phthalocyanine blue

    Science.gov (United States)

    Schreiver, Ines; Hutzler, Christoph; Laux, Peter; Berlien, Hans-Peter; Luch, Andreas

    2015-08-01

    Since laser treatment of tattoos is the favored method for the removing of no longer wanted permanent skin paintings, analytical, biokinetics and toxicological data on the fragmentation pattern of commonly used pigments are urgently required for health safety reasons. Applying dynamic headspace—gas chromatography with mass spectrometric detection (DHS—GC/MS) and comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GCxGC—ToF-MS), we identified 1,2-benzene dicarbonitrile, benzonitrile, benzene, and the poisonous gas hydrogen cyanide (HCN) as main fragmentation products emerging dose-dependently upon ruby laser irradiation of the popular blue pigment copper phthalocyanine in suspension. Skin cell viability was found to be significantly compromised at cyanide levels of ≥1 mM liberated during ruby laser irradiation of >1.5 mg/ml phthalocyanine blue. Further, for the first time we introduce pyrolysis-GC/MS as method suitable to simulate pigment fragmentation that may occur spontaneously or during laser removal of organic pigments in the living skin of tattooed people. According to the literature such regular tattoos hold up to 9 mg pigment/cm2 skin.

  8. Formation of highly toxic hydrogen cyanide upon ruby laser irradiation of the tattoo pigment phthalocyanine blue.

    Science.gov (United States)

    Schreiver, Ines; Hutzler, Christoph; Laux, Peter; Berlien, Hans-Peter; Luch, Andreas

    2015-08-05

    Since laser treatment of tattoos is the favored method for the removing of no longer wanted permanent skin paintings, analytical, biokinetics and toxicological data on the fragmentation pattern of commonly used pigments are urgently required for health safety reasons. Applying dynamic headspace-gas chromatography with mass spectrometric detection (DHS-GC/MS) and comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GCxGC-ToF-MS), we identified 1,2-benzene dicarbonitrile, benzonitrile, benzene, and the poisonous gas hydrogen cyanide (HCN) as main fragmentation products emerging dose-dependently upon ruby laser irradiation of the popular blue pigment copper phthalocyanine in suspension. Skin cell viability was found to be significantly compromised at cyanide levels of ≥1 mM liberated during ruby laser irradiation of >1.5 mg/ml phthalocyanine blue. Further, for the first time we introduce pyrolysis-GC/MS as method suitable to simulate pigment fragmentation that may occur spontaneously or during laser removal of organic pigments in the living skin of tattooed people. According to the literature such regular tattoos hold up to 9 mg pigment/cm(2) skin.

  9. The Effect of Gravity Axis Orientation on the Growth of Phthalocyanine Thin Films

    Science.gov (United States)

    Pearson, Earl F.

    1996-01-01

    Experimentally, many of the functions of electrical circuits have been demonstrated using optical circuits and, in theory, all of these functions may be accomplished using optical devices made of nonlinear optical materials. Actual construction of nonlinear optical devices is one of the most active areas in all optical research being done at this time. Physical vapor transport (PVT) is a promising technique for production of thin films of a variety of organic and inorganic materials. Film optical quality, orientation of microcrystals, and thickness depends critically on type of material, pressure of buffer gas and temperature of deposition. An important but understudied influence on film characteristics is the effect of gravity-driven buoyancy. Frazier, Hung, Paley, Penn and Long have recently reported mathematical modelling of the vapor deposition process and tested the predictions of the model on the thickness of films grown by PVT of 6-(2-methyl-4-nitroanilino)-2,4-hexadiyn-l-ol (DAMNA). In an historic experiment, Debe, et. al. offered definitive proof that copper phthalocyanine films grown in a low gravity environment are denser and more ordered than those grown at 1 g. This work seeks to determine the influence on film quality of gravity driven buoyancy in the low pressure PVT film growth of metal-free phthalocyanine.

  10. Photophysical studies of zinc phthalocyanine and chloroaluminum phthalocyanine incorporated into liposomes in the presence of additives

    Directory of Open Access Journals (Sweden)

    S.M.T. Nunes

    2004-02-01

    Full Text Available The photophysical properties of zinc phthalocyanine (ZnPC and chloroaluminum phthalocyanine (AlPHCl incorporated into liposomes of dimyristoyl phosphatidylcholine in the presence and absence of additives such as cholesterol or cardiolipin were studied by time-resolved fluorescence, laser flash photolysis and steady-state techniques. The absorbance of the drugs changed linearly with drug concentration, at least up to 5.0 µM in homogeneous and heterogeneous media, indicating that aggregation did not occur in these media within this concentration range. The incorporation of the drugs into liposomes increases the dimerization constant by one order of magnitude (for ZnPC, 3.6 x 10(4 to 1.0 x 10(5 M-1 and for AlPHCl, 3.7 x 10(4 to 1.5 x 10(5 M-1, but this feature dose does not rule out the use of this carrier, since the incorporation of these hydrophobic drugs into liposomes permits their systemic administration. Probe location in biological membranes and predominant positions of the phthalocyanines in liposomes were inferred on the basis of their fluorescence and triplet state properties. Both phthalocyanines are preferentially distributed in the internal regions of the liposome bilayer. The additives affect the distribution of these drugs within the liposomes, a fact that controls their delivery when both are used in a biological medium, retarding their release. The addition of the additives to the liposomes increases the internalization of phthalocyanines. The interaction of the drugs with a plasma protein, bovine serum albumin, was examined quantitatively by the fluorescence technique. The results show that when the drugs were incorporated into small unilamellar liposomes, the association with albumin was enhanced when compared with organic media, a fact that should increase the selectivity of tumor targeting by these phthalocyanines (for ZnPC, 0.71 x 10(6 to 1.30 x 10(7 M-1 and for AlPHCl, 4.86 x 10(7 to 3.10 x 10(8 M-1.

  11. Kinetic response study in chemiresistive gas sensor based on carbon nanotube surface functionalized with substituted phthalocyanines

    Science.gov (United States)

    Sharma, Anshul Kumar; Kumar, Pankaj; Saini, Rajan; Bedi, R. K.; Mahajan, Aman

    2016-05-01

    A kind of hybrid material is prepared by functionalizing multi-wall carbon nanotubes (MWCNTs-COOH) with substituted copper phthalocyanine and the formation of CuPcOC8/MWCNTs-COOH hybrid is confirmed by scanning electron microscopy and transmission electron microscopy. The results indicated that on the surface of nanotubes substituted CuPcOC8 derivatives has been successfully anchored through π-π stacking interaction. The gas sensing application of the fabricated hybrid material is tested upon exposure to different hazardous species, specifically NO2, NO, Cl2 and NH3 at operating temperature of 150˚C. It has been demonstrated that for Cl2 minimum detection limit of CuPcOC8/MWCNTs-COOH hybrid is 100 ppb. The response of hybrid sensor is found to be increased with increase in the concentration of Cl2.

  12. Thin films of tetrafluorosubstituted cobalt phthalocyanine: Structure and sensor properties

    Energy Technology Data Exchange (ETDEWEB)

    Klyamer, Darya D.; Sukhikh, Aleksandr S. [Nikolaev Institute of Inorganic Chemistry SB RAS, Lavrentiev Pr. 3, Novosibirsk 630090 (Russian Federation); Novosibirsk State University, Pirogova Str. 2 (Russian Federation); Krasnov, Pavel O. [Nikolaev Institute of Inorganic Chemistry SB RAS, Lavrentiev Pr. 3, Novosibirsk 630090 (Russian Federation); Gromilov, Sergey A. [Nikolaev Institute of Inorganic Chemistry SB RAS, Lavrentiev Pr. 3, Novosibirsk 630090 (Russian Federation); Novosibirsk State University, Pirogova Str. 2 (Russian Federation); Morozova, Natalya B. [Nikolaev Institute of Inorganic Chemistry SB RAS, Lavrentiev Pr. 3, Novosibirsk 630090 (Russian Federation); Basova, Tamara V., E-mail: basova@niic.nsc.ru [Nikolaev Institute of Inorganic Chemistry SB RAS, Lavrentiev Pr. 3, Novosibirsk 630090 (Russian Federation); Novosibirsk State University, Pirogova Str. 2 (Russian Federation)

    2016-05-30

    Highlights: • Thin films of tetrafluorosubstituted cobalt phthalocyanine were studied. • The effect of fluorine substituents to the films structure and properties was verified. • The sensor response of tetrafluorosubstituted phthalocyanine toward NH{sub 3} was studied. • The structure of analyte/phthalocyanine complex was analysed using DFT calculations. - Abstract: In this work, thin films of tetrafluorosubstituted cobalt phthalocyanine (CoPcF{sub 4}) were prepared by organic molecular beam deposition and their structure was studied using UV–vis, polarization dependent Raman spectroscopy, XRD and atomic force microscopy. Quantum chemical calculations (DFT) have been employed in order to determine the detailed assignment of the bands in the CoPcF{sub 4} IR and Raman spectra. The electrical sensor response of CoPcF{sub 4} films to ammonia vapours was investigated and compared with that of unsubstituted cobalt phthalocyanine films. In order to explain the difference in sensitivity of the unsubstituted and fluorinated phthalocyanines to ammonia, the nature and properties of chemical binding between CoPc derivatives and NH{sub 3} were described by quantum-chemical calculations utilizing DFT method. The effect of post-deposition annealing on surface morphology and gas sensing properties of CoPcF{sub 4} films was also studied.

  13. Stark effect on holes in the absorption spectra of phthalocyanine and the aluminum-phthalocyanine complex in polymer matrices

    Science.gov (United States)

    Ulitskiĭ, N. I.; Snegirev, E. P.; Personov, R. I.

    2002-06-01

    The effect of an external electric field on narrow spectral holes in S1←S0 absorption bands of molecules of free-base phthalocyanine and its complex with Al in polyvinyl butyral films at 4.2 K was studied. It was found that the average values of the change in the electric dipole moment due to phototransitions in the free-base phthalocyanine and its complex amount to 0.135 and 0.145 D, respectively. Both these values considerably exceed the relevant values for phthalocyanine complexes with Zn and Mg in the same matrix. Possible causes of the observed effects are discussed. Most probably, they are related to the differences in the structure of the central part of phthalocyanine-type molecules.

  14. Length-dependent thermal transport in one-dimensional self-assembly of planar π-conjugated molecules

    Science.gov (United States)

    Tang, Hao; Xiong, Yucheng; Zu, Fengshuo; Zhao, Yang; Wang, Xiaomeng; Fu, Qiang; Jie, Jiansheng; Yang, Juekuan; Xu, Dongyan

    2016-06-01

    This work reports a thermal transport study in quasi-one-dimensional organic nanostructures self-assembled from conjugated planar molecules via π-π interactions. Thermal resistances of single crystalline copper phthalocyanine (CuPc) and perylenetetracarboxylic diimide (PTCDI) nanoribbons are measured via a suspended thermal bridge method. We experimentally observed the deviation from the linear length dependence for the thermal resistance of single crystalline β-phase CuPc nanoribbons, indicating possible subdiffusion thermal transport. Interestingly, a gradual transition to the linear length dependence is observed with the increase of the lateral dimensions of CuPc nanoribbons. The measured thermal resistance of single crystalline CuPc nanoribbons shows an increasing trend with temperature. However, the trend of temperature dependence of thermal resistance is reversed after electron irradiation, i.e., decreasing with temperature, indicating that the single crystalline CuPc nanoribbons become `amorphous'. Similar behavior is also observed for PTCDI nanoribbons after electron irradiation, proving that the electron beam can induce amorphization of single crystalline self-assembled nanostructures of planar π-conjugated molecules. The measured thermal resistance of the `amorphous' CuPc nanoribbon demonstrates a roughly linear dependence on the nanoribbon length, suggesting that normal diffusion dominates thermal transport.This work reports a thermal transport study in quasi-one-dimensional organic nanostructures self-assembled from conjugated planar molecules via π-π interactions. Thermal resistances of single crystalline copper phthalocyanine (CuPc) and perylenetetracarboxylic diimide (PTCDI) nanoribbons are measured via a suspended thermal bridge method. We experimentally observed the deviation from the linear length dependence for the thermal resistance of single crystalline β-phase CuPc nanoribbons, indicating possible subdiffusion thermal transport

  15. Electronic transport properties of (fluorinated) metal phthalocyanine

    KAUST Repository

    Fadlallah, M M

    2015-12-21

    The magnetic and transport properties of the metal phthalocyanine (MPc) and F16MPc (M = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn and Ag) families of molecules in contact with S–Au wires are investigated by density functional theory within the local density approximation, including local electronic correlations on the central metal atom. The magnetic moments are found to be considerably modified under fluorination. In addition, they do not depend exclusively on the configuration of the outer electronic shell of the central metal atom (as in isolated MPc and F16MPc) but also on the interaction with the leads. Good agreement between the calculated conductance and experimental results is obtained. For M = Ag, a high spin filter efficiency and conductance is observed, giving rise to a potentially high sensitivity for chemical sensor applications.

  16. Spin doping using transition metal phthalocyanine molecules

    Science.gov (United States)

    Atxabal, A.; Ribeiro, M.; Parui, S.; Urreta, L.; Sagasta, E.; Sun, X.; Llopis, R.; Casanova, F.; Hueso, L. E.

    2016-12-01

    Molecular spins have become key enablers for exploring magnetic interactions, quantum information processes and many-body effects in metals. Metal-organic molecules, in particular, let the spin state of the core metal ion to be modified according to its organic environment, allowing localized magnetic moments to emerge as functional entities with radically different properties from its simple atomic counterparts. Here, using and preserving the integrity of transition metal phthalocyanine high-spin complexes, we demonstrate the magnetic doping of gold thin films, effectively creating a new ground state. We demonstrate it by electrical transport measurements that are sensitive to the scattering of itinerant electrons with magnetic impurities, such as Kondo effect and weak antilocalization. Our work expands in a simple and powerful way the classes of materials that can be used as magnetic dopants, opening a new channel to couple the wide range of molecular properties with spin phenomena at a functional scale.

  17. Immunosuppressive effects of silicon phthalocyanine photodynamic therapy.

    Science.gov (United States)

    Reddan, J C; Anderson, C Y; Xu, H; Hrabovsky, S; Freye, K; Fairchild, R; Tubesing, K A; Elmets, C A

    1999-07-01

    The purpose of this study was to determine if silicon phthalocyanine 4 (Pc 4), a second-generation photosensitizer being evaluated for the photodynamic therapy (PDT) of solid tumors, was immunosuppressive. Mice treated with Pc 4 PDT 3 days before dinitrofluorobenzene sensitization showed significant suppression of their cell-mediated immune response when compared to mice that were not exposed to PDT. The response was dose dependent, required both Pc 4 and light and occurred at a skin site remote from that exposed to the laser. The immunosuppression could not be reversed by in vivo pre-treatment of mice with antibodies to tumor necrosis factor-alpha or interleukin-10. These results provide evidence that induction of cell-mediated immunity is suppressed after Pc 4 PDT. Strategies that prevent PDT-mediated immunosuppression may therefore enhance the efficacy of this therapeutic modality.

  18. The effect of metal ions on the photophysical and photochemical property of phenylthio bromo metal phthalocyanines

    Science.gov (United States)

    Pan, Sujuan; Shen, Pingping; Ma, Dongdong; Wang, Yuhua; Zhang, Tiantian; Chen, Kuizhi; Yang, Hongqin; Xie, Shusen; Peng, Yiru

    2016-10-01

    Phthalocyanines have attracted great attention because of their applications in material science including electro-optical devices, electrochromic display, and photodynamic therapy (PDT) of cancer. In addition, the Pcs exhibit great flexibility of chemical structure modification enabled by either peripheral substituents or metal ions co-ordination to central cavity of highly conjugated tetrapyrrolic macrocycles. However, because of the hydrophobic nature of the phthalocyanine ring, Pcs have strong tendency to aggregate in solution, which limited their applications. To overcome this problem, the introduction of dendritic wedge to peripheral positions of phthalocyanines can prevent the formation of aggregation to some extent. The preparation procedure involved the modification of the zinc (II) and magnesium (II) phthalocyanines with peripherally dendritic substitutions. The photophysical and photochemical properties of dendritic phthalocyanines were studied by UV/Vis and fluorescence spectroscopic methods. Compared with the magnesium (II) phthalocyanine, the intensity of Q band of zinc (II) phthalocyanine was increased but no obviously position changes was observed. Furthermore, the zinc (II) phthalocyanine exhibited relatively higher fluorescence intensity than the magnesium (II) phthalocyanine. The fluorescence quantum yield and lifetimes of magnesium (II) phthalocyanine was clearly longer than that of zinc (II) phthalocyanine. As the better photosensitizer, the zinc (II) phthalocyanine has higher singlet oxygen quantum yield owning superior performance. This results indicated that the singlet oxygen quantum yield would be effected by the nature of metal ions.

  19. Realization of size controllable graphene micro/nanogap with a micro/nanowire mask method for organic field-effect transistors

    DEFF Research Database (Denmark)

    Liao, Zhiyu; Wan, Qing; Liu, Huixuan;

    2011-01-01

    A size controllable graphene micro/nanogap fabrication method using micro/nanowire as mask is presented. The gap dimension can be adjusted by the diameter of the mask wire. As a typical application, copper phthalocyanine (CuPc) film organic field-effect transistors (OFETs) were fabricated...... with the graphene micro/nanogap bottom electrodes. The ultrathin thickness of the graphene, combined with its good compatibility with organic semiconductors, and high electrical conductivity produced high-performance CuPc film device with mobility at 0.053 cm(2)/Vs and on/off ratio at 10(5), showing promising...

  20. Improvement of organic solar cell performances using a zinc oxide anode coated by an ultrathin metallic layer

    Science.gov (United States)

    Bernède, J. C.; Berredjem, Y.; Cattin, L.; Morsli, M.

    2008-02-01

    The authors have achieved an efficient organic solar cell based on copper phthalocyanine (CuPc) layer as donor and fullerene (C60) as acceptor. The aluminum doped zinc oxide (ZnO:Al) instead of indium tin oxide (ITO) is used as the anode. An ultrathin gold film is introduced among ZnO:Al, transparent conductor oxide, and the CuPc donor layer. We show that the power conversion efficiency of this cell is enhanced by one order of magnitude compared to that achieved with a ZnO anode without ultrathin gold film. Therefore, the power conversion efficiency of this cell is comparable to that with an ITO anode.

  1. Sequential biphotonic processes: photochemical reactivity of phthalocyanine radicals

    Energy Technology Data Exchange (ETDEWEB)

    Van Vlierberge, B.; Ferraudi, G.

    1987-01-28

    Results of a study of the photochemistry of Rh(III), Al(III), and Zn(II) phthalocyanine cation radicals are reported here. The radicals were generated in a flash photolysis apparatus, which employs two flash-lamp-pump dye lasers. This excitation of the metallophthalocyanines at wavelengths of the phthalocyanine's Q band produced the long-lived triplet state. Irradiation of the phthalocyanine radicals led to rapid (t less than 1 ..mu..s) decomposition of these species followed by a partial recovery of the radical concentration. The dependence of radical yield on medium conditions was noted, and this dependence was probably attributable to an increase in the yield of the reactive excited state and/or a decrease in the rate of excited-state relaxation in changing from protic to aprotic media or replacing D/sub 2/O by H/sub 2/O. 10 references, 3 figures, 2 tables.

  2. Optical Constants of Palladium Phthalocyanine Derivative Thin Films

    Institute of Scientific and Technical Information of China (English)

    吴谊群; 顾冬红; 干福熹; 王俊东; 陈耐生

    2002-01-01

    Ellipsometric parameters ora series of spin-coated thin films of palladium phthalocyanine derivatives with bromine and tetraalkoxyl substitutes (PdPc(OC8H17)4Brm, m = 0, 2, 3, 4) are determined from a rotating analyserpolarizer type of scanning ellipsometer. The optical, dielectric constants and absorption coefficients of the films in the 500-800nm wavelength region are reported. The results show that refractive index N (N = n- k),dielectric constant ε (ε =ε1 -ε2) and absorption coefficient α in the region 500-800nm are influenced by bromine atom substituted on the conjugated phthalocyanine ring regularly. It is found that there is approximately a linear relationship between the resonance absorption wavelengths of the films and the number of bromine atoms substituted on the phthalocyanine ring.

  3. Photoelectric characteristics of lead phthalocyanine/titanium oxide structures

    CERN Document Server

    Ray, A K; Hodgson, S N B

    2003-01-01

    A study has been carried out into the conduction, charge transfer/electron injection and photovoltaic conversion properties of TiO sub 2 -lead phthalocyanine (PbPc) heterojunctions. The results indicate that although the heterojunction area, and hence overall conversion efficiency, was low for the planar device structures used in the investigation, electron injection and effective charge separation across the dye-TiO sub 2 interface was achieved, with open circuit voltages in the region of 0.3 V. The conversion efficiency was found to be a function of the thickness of the phthalocyanine layer, increasing by a factor of more than 30 times as the thickness of the dye layer was reduced from 500 to 100 nm. The results suggest that under appropriate deposition conditions, to ensure effective coating of the inorganic phase, such phthalocyanine dyes may offer potential for use in dye sensitized photovoltaic cells.

  4. Copper hypersensitivity.

    Science.gov (United States)

    Fage, Simon W; Faurschou, Annesofie; Thyssen, Jacob P

    2014-10-01

    The world production of copper is steadily increasing. Although humans are widely exposed to copper-containing items on the skin and mucosa, allergic reactions to copper are only infrequently reported. To review the chemistry, biology and accessible data to clarify the implications of copper hypersensitivity, a database search of PubMed was performed with the following terms: copper, dermatitis, allergic contact dermatitis, contact hypersensitivity, contact sensitization, contact allergy, patch test, dental, IUD, epidemiology, clinical, and experimental. Human exposure to copper is relatively common. As a metal, it possesses many of the same qualities as nickel, which is a known strong sensitizer. Cumulative data on subjects with presumed related symptoms and/or suspected exposure showed that a weighted average of 3.8% had a positive patch test reaction to copper. We conclude that copper is a very weak sensitizer as compared with other metal compounds. However, in a few and selected cases, copper can result in clinically relevant allergic reactions.

  5. Synthesis and Photoconductivity of Nanosized Phthalocyanine

    Institute of Scientific and Technical Information of China (English)

    Shuguang BIAN; Xianggao LI; Lei SHAO; Jianfeng CHEN

    2006-01-01

    Functional phthalocyanine (Pc) compounds of H2Pc, TiOPc, FePc and ClAlPc were synthesized with a yield of 46.7%, 91.2%, 37.4% and 34.0%, respectively. Nanosized TiOPc was synthesized via a one-step sol-gel method and effects of surfactant doses, nucleation temperature on TiOPc particle size and photoconductivity were investigated. When m(PEG): m(TiOPc) was 0.1 and nucleation temperature was 0℃, the as-obtained TiOPc had the smallest particle size and largest specific surface area, which were 60 nm and 83 m2/g, respectively. TiOPc synthesized under these conditions also exhibits excellent photoconductivity with charging potential V0, dark decay speed Rd and energy for half-discharging of potential E1/2 being 1160 V, 30 V/s and 0.6 lx·s, respectively.

  6. A Novel Gas Sensor Transducer Based on Phthalocyanine Heterojunction Devices

    OpenAIRE

    Marcel Bouvet; Janis Latvels; Egils Fonavs; Rorijs Dobulans; Vicente Parra; Inta Muzikante

    2007-01-01

    Experimental data concerning the changes in the current-voltage (I-V) performances of a molecular material-based heterojunction consisting of hexadecafluorinated nickel phthalocyanine (Ni(F16Pc)) and nickel phthalocyanine (NiPc), (Au|Ni(F16Pc)|NiPc|Al) are introduced as an unprecedented principle of transduction for gas sensing performances. The respective n- and p-type doped-insulator behaviors of the respective materials are supported, owing to the observed changes in surface potential (usi...

  7. Copper transport.

    Science.gov (United States)

    Linder, M C; Wooten, L; Cerveza, P; Cotton, S; Shulze, R; Lomeli, N

    1998-05-01

    In adult humans, the net absorption of dietary copper is approximately 1 mg/d. Dietary copper joins some 4-5 mg of endogenous copper flowing into the gastrointestinal tract through various digestive juices. Most of this copper returns to the circulation and to the tissues (including liver) that formed them. Much lower amounts of copper flow into and out of other major parts of the body (including heart, skeletal muscle, and brain). Newly absorbed copper is transported to body tissues in two phases, borne primarily by plasma protein carriers (albumin, transcuprein, and ceruloplasmin). In the first phase, copper goes from the intestine to the liver and kidney; in the second phase, copper usually goes from the liver (and perhaps also the kidney) to other organs. Ceruloplasmin plays a role in this second phase. Alternatively, liver copper can also exit via the bile, and in a form that is less easily reabsorbed. Copper is also present in and transported by other body fluids, including those bathing the brain and central nervous system and surrounding the fetus in the amniotic sac. Ceruloplasmin is present in these fluids and may also be involved in copper transport there. The concentrations of copper and ceruloplasmin in milk vary with lactational stage. Parallel changes occur in ceruloplasmin messenger RNA expression in the mammary gland (as determined in pigs). Copper in milk ceruloplasmin appears to be particularly available for absorption, at least in rats.

  8. Copper hypersensitivity

    DEFF Research Database (Denmark)

    Fage, Simon W; Faurschou, Annesofie; Thyssen, Jacob P

    2014-01-01

    hypersensitivity, a database search of PubMed was performed with the following terms: copper, dermatitis, allergic contact dermatitis, contact hypersensitivity, contact sensitization, contact allergy, patch test, dental, IUD, epidemiology, clinical, and experimental. Human exposure to copper is relatively common...

  9. Synthesis and photophysical properties of metal anthraquinone phthalocyanine

    Institute of Scientific and Technical Information of China (English)

    Yi Ru Peng; Kui Zhi Chen; Jia Bao Wen; Ji Cheng Shi; Bao Quan Huang

    2007-01-01

    A novel anthraquinone phthalocyanine Al(Ⅲ) 4 and Co(Ⅱ) 5 were synthesized and characterized by elemental analysis, IR, UV/vis, 1H NMR, HPLC and MS. The photophysical properties of the two metal complexes were studied and compared by fluorescence spectrum method.

  10. A Fulleropyrrolidine-phthalocyanine dyad for photovoltaic applications

    NARCIS (Netherlands)

    Loi, M.A.; Denk, P.; Hoppe, H.; Neugebauer, H.; Meissner, D.; Winder, C.; Brabec, C.J.; Sariciftci, N.S.; Gouloumis, A.; Vázquez, P.; Torres, T.

    2003-01-01

    We report on photophysical properties of a novel dyad molecule having as antenna/donor a Zn-phthalocyanine derivative and as acceptor a C60 derivative covalently attached. We found evidences for long living photoinduced electron transfer in solid state. Photovoltaic action of thin film devices of th

  11. A fulleropyrrolidine-phthalocyanine dyad for photovoltaic applications

    NARCIS (Netherlands)

    Loi, MA; Denk, P; Hoppe, H; Neugebauer, H; Meissner, D; Winder, C; Brabec, CJ; Sariciftci, NS; Gouloumis, A; Vazquez, P; Torres, T

    2003-01-01

    We report on photophysical properties of a novel dyad molecule having as antenna/donor a Zn-phthalocyanine derivative and as acceptor a C-60 derivative covalently attached. We found evidences for long living photoinduced electron transfer in solid state. Photovoltaic action of thin film devices of t

  12. A Fulleropyrrolidine-phthalocyanine dyad for photovoltaic applications

    NARCIS (Netherlands)

    Loi, M.A.; Denk, P.; Hoppe, H.; Neugebauer, H.; Meissner, D.; Winder, C.; Brabec, C.J.; Sariciftci, N.S.; Gouloumis, A.; Vázquez, P.; Torres, T.

    2003-01-01

    We report on photophysical properties of a novel dyad molecule having as antenna/donor a Zn-phthalocyanine derivative and as acceptor a C60 derivative covalently attached. We found evidences for long living photoinduced electron transfer in solid state. Photovoltaic action of thin film devices of

  13. Active and passive control of zinc phthalocyanine photodynamics

    NARCIS (Netherlands)

    Sharma, D.; Huijser, J.M.; Savolainen, J.; Steen, G.W.; Herek, J.L.

    2013-01-01

    In this work we report on the ultrafast photodynamics of the photosensitizer zinc phthalocyanine (ZnPc) and manipulation thereof. Two approaches are followed: active control via pulse shaping and passive control via strategic manipulation in the periphery of the molecular structure. The objective of

  14. A Fulleropyrrolidine-phthalocyanine dyad for photovoltaic applications

    NARCIS (Netherlands)

    Loi, M.A.; Denk, P.; Hoppe, H.; Neugebauer, H.; Meissner, D.; Winder, C.; Brabec, C.J.; Sariciftci, N.S.; Gouloumis, A.; Vázquez, P.; Torres, T.

    2003-01-01

    We report on photophysical properties of a novel dyad molecule having as antenna/donor a Zn-phthalocyanine derivative and as acceptor a C60 derivative covalently attached. We found evidences for long living photoinduced electron transfer in solid state. Photovoltaic action of thin film devices of th

  15. Silicon phthalocyanine 4 phototoxicity in Trichophyton rubrum.

    Science.gov (United States)

    Lam, Minh; Dimaano, Matthew L; Oyetakin-White, Patricia; Retuerto, Mauricio A; Chandra, Jyotsna; Mukherjee, Pranab K; Ghannoum, Mahmoud A; Cooper, Kevin D; Baron, Elma D

    2014-06-01

    Trichophyton rubrum is the leading pathogen that causes long-lasting skin and nail dermatophyte infections. Currently, topical treatment consists of terbinafine for the skin and ciclopirox for the nails, whereas systemic agents, such as oral terbinafine and itraconazole, are also prescribed. These systemic drugs have severe side effects, including liver toxicity. Topical therapies, however, are sometimes ineffective. This led us to investigate alternative treatment options, such as photodynamic therapy (PDT). Although PDT is traditionally recognized as a therapeutic option for treating a wide range of medical conditions, including age-related macular degeneration and malignant cancers, its antimicrobial properties have also received considerable attention. However, the mechanism(s) underlying the susceptibility of dermatophytic fungi to PDT is relatively unknown. As a noninvasive treatment, PDT uses a photosensitizing drug and light, which, in the presence of oxygen, results in cellular destruction. In this study, we investigated the mechanism of cytotoxicity of PDT in vitro using the silicon phthalocyanine (Pc) 4 [SiPc(OSi(CH3)2(CH2)3N(CH3)2)(OH)] in T. rubrum. Confocal microscopy revealed that Pc 4 binds to cytoplasmic organelles, and upon irradiation, reactive oxygen species (ROS) are generated. The impairment of fungal metabolic activities as measured by an XTT (2,3-bis[2-methoxy-4-nitro-5-sulfophenyl]-2H-tetrazolium-5-carboxyanilide inner salt) assay indicated that 1.0 μM Pc 4 followed by 670 to 675 nm light at 2.0 J/cm(2) reduced the overall cell survival rate, which was substantiated by a dry weight assay. In addition, we found that this therapeutic approach is effective against terbinafine-sensitive (24602) and terbinafine-resistant (MRL666) strains. These data suggest that Pc 4-PDT may have utility as a treatment for dermatophytosis.

  16. Phthalocyanine photosensitizers as contrast agents for in vivo photoacoustic tumor imaging.

    Science.gov (United States)

    Attia, Amalina Bte Ebrahim; Balasundaram, Ghayathri; Driessen, Wouter; Ntziachristos, Vasilis; Olivo, Malini

    2015-02-01

    There is a need for contrast agents for non-invasive diagnostic imaging of tumors. Herein, Multispectral Optoacoustic Tomography (MSOT) was employed to evaluate phthalocyanines commonly used in photodynamic therapy as photoacoustic contrast agents. We studied the photoacoustic activity of three water-soluble phthalocyanine photosensitizers: phthalocyanine tetrasulfonic acid (PcS4), Zn(II) phthalocyanine tetrasulfonic acid (ZnPcS4) and Al(III) phthalocyanine chloride tetrasulfonic acid (AlPcS4) in phantom and in tumor-bearing mice to investigate the biodistribution and fate of the phthalocyanines in the biological tissues. PcS4 was observed to grant good contrast between the different reticuloendothelial organs and accumulate in the tumor within an hour of post-administration. ZnPcS4 and AlPcS4 offered little contrast in photoacoustic signals between the organs. PcS4 is a promising photoacoustic contrast agent and can be exploited as a photodiagnostic agent.

  17. Layer-by-layer assembled highly absorbing hundred-layer films containing a phthalocyanine dye: Fabrication and photosensibilization by thermal treatment

    Energy Technology Data Exchange (ETDEWEB)

    Sergeeva, Alena S., E-mail: alenasergeeva@mail.ru [Saratov State University, Astrakhanskaya 83, 410012 Saratov (Russian Federation); Fraunhofer Institute for Cell Therapy and Immunology, Branch Bioanalytics and Bioprocesses (Fraunhofer IZI-BB), Muehlenberg 13, 14476 Potsdam (Germany); Volkova, Elena K., E-mail: ekvolkova87@rambler.ru [Saratov State University, Astrakhanskaya 83, 410012 Saratov (Russian Federation); Bratashov, Daniil N., E-mail: dn2010@gmail.com [Saratov State University, Astrakhanskaya 83, 410012 Saratov (Russian Federation); Shishkin, Mikhail I., E-mail: shishkin1mikhail@gmail.com [Saratov State University, Astrakhanskaya 83, 410012 Saratov (Russian Federation); Atkin, Vsevolod S., E-mail: ceba91@list.ru [Saratov State University, Astrakhanskaya 83, 410012 Saratov (Russian Federation); Markin, Aleksey V., E-mail: markinav@mail.ru [Saratov State University, Astrakhanskaya 83, 410012 Saratov (Russian Federation); Skaptsov, Aleksandr A., E-mail: skaptsov@yandex.ru [Saratov State University, Astrakhanskaya 83, 410012 Saratov (Russian Federation); Volodkin, Dmitry V., E-mail: dmitry.volodkin@izi-bb.fraunhofer.de [Fraunhofer Institute for Cell Therapy and Immunology, Branch Bioanalytics and Bioprocesses (Fraunhofer IZI-BB), Muehlenberg 13, 14476 Potsdam (Germany); Gorin, Dmitry A., E-mail: gorinda@mail.ru [Saratov State University, Astrakhanskaya 83, 410012 Saratov (Russian Federation)

    2015-05-29

    Highly absorbing hundred-layer films based on poly(diallyldimethylammonium chloride) (PDADMAC) of various molecular weights and on sulfonated copper phthalocyanine (CuPcTs) were prepared using layer-by-layer assembly. The multilayer films grew linearly up to 54 bilayers, indicating that the same amount of CuPcTs was adsorbed at each deposition step. This amount, however, was dependent on the molecular weight of PDADMAC in the range 100-500 kDa: the higher the molecular weight, the more CuPcTs molecules were adsorbed. This can be explained by the larger surface charge number density specific to longer polymer chains. Domains of pure PDADMAC and of the PDADMAC/CuPcTs complex were formed in the films during the assembly. Uniform distribution of CuPcTs over the films could be achieved by thermal treatment, leading to an α → β phase transition in phthalocyanine at 300 °C. Annealing caused changes in the film absorbance spectra, resulting in a 30-nm red shift of the peak maxima and in a strong (up to 62%) decrease in optical density. Thermogravimetric analysis revealed thermodegradation of PDADMAC during annealing above 270 °C, giving rise to micrometer-sized cracks within the films, as evidenced by scanning electron microscopy. - Highlights: • The films exhibit the linear dependence of the adsorption on the bilayer number varied from 2 until 54. • Polyelectrolyte of the highest MW shows the maximal adsorption of copper phthalocyanine molecules. • Annealing of the films causes a red-shift of the maxima in the absorbance spectra. • Cracks and micropores emerged in the multilayer films during the annealing.

  18. Unmetallated and metallated phthalocyanines bearing oxadiazole groups: Synthesis, photophysical and photochemical studies

    Energy Technology Data Exchange (ETDEWEB)

    Nas, Asiye [Department of Chemistry, Karadeniz Technical University, 61080 Trabzon (Turkey); Kantekin, Halit, E-mail: halit@ktu.edu.tr [Department of Chemistry, Karadeniz Technical University, 61080 Trabzon (Turkey); Durmuş, Mahmut [Gebze Institute of Technology, Department of Chemistry, PO Box 141, Gebze, 41400 Kocaeli (Turkey); Gümrükçüoğlu, Nurhan [Department of Chemistry, Karadeniz Technical University, 61080 Trabzon (Turkey)

    2014-10-15

    Unmetallated (4) and metallated (zinc(II), cobalt(II), lead(II)) phthalocyanines (5–7) carrying four 4-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenoxy) groups on the peripheral positions were synthesized by cyclotetramerization of 4-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenoxy)phthalonitrile (3) in the presence of corresponding metal salts (zinc(II) acetate, cobalt(II) chloride, lead(II) oxide) for metallated and without any metal for unmetallated phthalocyanines. The obtained organo-soluble phthalocyanines were characterized by infrared, electronic absorption, nuclear magnetic resonance and mass spectral techniques and elemental analysis as well. The photophysical and photochemical properties of newly synthesized tetra-substituted unmetallated (4), zinc(II) (5) and lead(II) (7) phthalocyanines were reported in N,N-dimetilformamid (DMF). The synthesized phthalocyanine compound 6 was not evaluated for photophysical and photochemical studies due to open shell and paramagnetic behavior of cobalt(II) metal ions in the phthalocyanine cavity. - Highlights: • Synthesis of unmetallated and metallated phthalocyanines. • Photophysical and photochemical properties of tetra-substituted phthalocyanines. • Characterization of organosoluble phthalocyanines by several spectral techniques.

  19. Photodynamic inactivation of prions by disulfonated hydroxyaluminium phthalocyanine.

    Science.gov (United States)

    Janouskova, Olga; Rakusan, Jan; Karaskova, Marie; Holada, Karel

    2012-11-01

    Sulfonated phthalocyanines (Pcs) are cyclic tetrapyrroles that constitute a group of photosensitizers. In the presence of visible light and diatomic oxygen, Pcs produce singlet oxygen and other reactive oxygen species that have known degradation effects on lipids, proteins and/or nucleic acids. Pcs have been used successfully in the treatment of bacterial, yeast and fungal infections, but their use in the photodynamic inactivation of prions has never been reported. Here, we evaluated the photodynamic activity of the disodium salt of disulfonated hydroxyaluminium phthalocyanine (PcDS) against mouse-adapted scrapie RML prions in vitro. PcDS treatment of RML brain homogenate resulted in a time- and dose-dependent inactivation of prions. The photodynamic potential of Pcs offers a new way to inactivate prions using biodegradable compounds at room temperature and normal pressure, which could be useful for treating thermolabile materials and liquids.

  20. Electrical Field Effects in Phthalocyanine Film Growth by Vapor Deposition

    Science.gov (United States)

    Banks, Curtis E.; Zhu, Shen; Frazier, Donald O.; Penn, Benjamin; Abdeldayem, Hossin; Hicks, Roslin; Sarkisov, Sergey

    1999-01-01

    Phthalocyanine, an organic material, is a very good candidate for non-linear optical application, such as high-speed switching and optical storage devices. Phthalocyanine films have been synthesized by vapor deposition on quartz substrates. Some substrates were coated with a very thin gold film for introducing electrical field. These films have been characterized by surface morphology, material structure, chemical and thermal stability, non-linear optical parameters, and electrical behaviors. The films have excellent chemical and optical stability. However, the surface of these films grown without electrical field shows flower-like morphology. When films are deposited under an electrical field ( an aligned structure is revealed on the surface. A comparison of the optical and electrical properties and the growth mechanism for these films grown with and without an electrical field will be discussed.

  1. Solution-Processable Silicon Phthalocyanines in Electroluminescent and Photovoltaic Devices.

    Science.gov (United States)

    Zysman-Colman, Eli; Ghosh, Sanjay S; Xie, Guohua; Varghese, Shinto; Chowdhury, Mithun; Sharma, Nidhi; Cordes, David B; Slawin, Alexandra M Z; Samuel, Ifor D W

    2016-04-13

    Phthalocyanines and their main group and metal complexes are important classes of organic semiconductor materials but are usually highly insoluble and so frequently need to be processed by vacuum deposition in devices. We report two highly soluble silicon phthalocyanine (SiPc) diester compounds and demonstrate their potential as organic semiconductor materials. Near-infrared (λ(EL) = 698-709 nm) solution-processed organic light-emitting diodes (OLEDs) were fabricated and exhibited external quantum efficiencies (EQEs) of up to 1.4%. Binary bulk heterojunction solar cells employing P3HT or PTB7 as the donor and the SiPc as the acceptor provided power conversion efficiencies (PCE) of up to 2.7% under simulated solar illumination. Our results show that soluble SiPcs are promising materials for organic electronics.

  2. Supramolecular Organization of Porphyrin and Phthalocyanine by Complementary Coordination

    Institute of Scientific and Technical Information of China (English)

    Yoshiaki; Kobuke; Masakuni; Fujita; Toshimasa; Sugimura; Akiharu; Satake

    2007-01-01

    1 Results We have already established a methodology of supramolecular organization of porphyrin and phthalocyanine by complementary coordination of the imidazolyl substituent to their metal centers.Since the stability constants reached a range of 1011 to 1012 M-1 in nonpolar solvents,it allowed construction of stable structures such as special pair of photosynthetic reaction center and light-harvesting antenna complex of photosynthetic bacteria.Here,we report one-dimensional array of porphyrin for the d...

  3. Supramolecular assemblies of pyridyl porphyrin and diazadithia phthalocyanine

    Directory of Open Access Journals (Sweden)

    OZER BEKAROGLU

    1999-08-01

    Full Text Available In this paper we report for the first time on a mixed complex between the cationic porphyrin 5, 10, 15, 20-tetra-N- -methyl-pyrydinium-p-il porphyrin (TMPyP and a new metal phthalocyanine with four 16-membered diazadithia macrocycles (denoted here as Pc16, in order to obtain an active complex with an intense absorption on the lower energy side of the visible spectrum and with a higher sensitivity in photodynamic therapy of cancer. The dimerization constant for Pc16 and also the ratio between the oscillator strengths for monomeric and dimeric forms of this compound, were evaluated. The ratio between these oscillator strengths was 2.01 showing a certain dimerization process. The Job mathematical method allowed the establishment of the stoichiometry and the formation constants for the heteroaggregates between the porphyrin and the phthalocy- anine (a diad between one phthalocyanine molecule and one porphyrin molecule and a triad between two phthalocyanine molecules and only one porphyrin molecule. The coulombic attraction resulting from the p-p interaction of the two highly conjugated macrocycles and from the interaction between the substituents, favors a face-to-face geometry.

  4. Inverted methoxypyridinium phthalocyanines for PDI of pathogenic bacteria.

    Science.gov (United States)

    Lourenço, Leandro M O; Sousa, Andreina; Gomes, Maria C; Faustino, Maria A F; Almeida, Adelaide; Silva, Artur M S; Neves, Maria G P M S; Cavaleiro, José A S; Cunha, Ângela; Tomé, João P C

    2015-10-01

    Phthalocyanines (Pc) are photoactive molecules that can absorb and emit light in a large range of the UV-Vis spectrum with recognized potential for medical applications. Considering the biomedical applications an important limitation of these compounds is their low solubility in water. The use of suitable pyridinium groups on Pc is a good strategy to solve this drawback and to make them more effective to photoinactivate Gram-negative bacteria via a photodynamic inactivation (PDI) approach. Herein, an easy synthetic access to obtain inverted tetra- and octa-methoxypyridinium phthalocyanines (compounds 5 and 6) and also their efficiency to photoinactivate a recombinant bioluminescent strain of Escherichia coli is described. The obtained results were compared with the ones obtained when more conventional thiopyridinium phthalocyanines (compounds 7 and 8) were used. This innovative study comparing thiopyridinium and inverted methoxypyridinium moieties on cationic Pc is reported for the first time taking into account the efficiency of singlet oxygen ((1)O2) generation, water solubility and uptake properties.

  5. Localization study of Co-phthalocyanines in cells by Raman micro(spectro)scopy

    NARCIS (Netherlands)

    Arzhantsev, S Y; Chikishev, A Y; Koroteev, N I; Greve, J; Otto, C; Sijtsema, N M

    1999-01-01

    An investigation of intracellular localization of Co-phthalocyanines is reported. The Raman images of K562 cells stained with phthalocyanine were acquired. To understand the peculiarities of the Raman images, measurements were performed at different z-axis positions. The intracellular concentration

  6. Localization study of co-phthalocyanines in cells by Raman micro(spectro)scopy

    NARCIS (Netherlands)

    Arzhantsev, S.Y.; Chikishev, A.Y.; Koroteev, N.I.; Greve, J.; Otto, C.; Sijtsema, N.M.

    1999-01-01

    An investigation of intracellular localization of Co-phthalocyanines is reported. The Raman images of K562 cells stained with phthalocyanine were acquired. To understand the peculiarities of the Raman images, measurements were performed at different z-axis positions. The intracellular concentration

  7. Photophysical properties of a novel axially substituted tetra-α-(pentyloxy) Titanium(IV) Phthalocyanine - Hematoxylin

    Science.gov (United States)

    Jiang, Yufeng; Lv, Huafei; Yu, Xinxin; Pan, Sujuan; Zhang, Tiantian; Huang, Yide; Wang, Yuhua; Xie, Shusen; Yang, Hongqin; Peng, Yiru

    2017-06-01

    Metal phthalocyanines (MPcs) are a very important class of widespread application compounds. They are not only used as dyes but also used as catalysts, data storage, electron charge carriers in photocopiers, photoconductors in chemical sensors, and photo-antenna devices in photosysthesis, photovoltaic cells. A particular application of Pcs is that it was used as a photosensitizers (PS) for treatment of certain cancer by photodynamic therapy of cancer and non-cancer diseases. However, the molecular aggregation of phthalocyanines, which is an intrinsic property of these large π-π conjugated systems, provides an efficient non-radioactive energy relaxation pathway, thereby shortening the excited state lifetimes, and reducing the photosensitizing and target efficiency. To overcome these problems, the introduction of axial ligands to phthalocyanine can prevent the formation of aggregation to some extend. In this paper, hematoxylin axially substituted tetra-α-(pentoxy) titanium (IV) phthalocyanine (TiPc(OC5H11)4-Hematoxylin) were characterized by elemental analysis, IR, 1H NMR, UV-Vis, fluorescence spectra. No obviously Q band change was observed after the hematoxylin was substituted at the peripheral position of substituted phthalocyanine ring. Because of the rigidity structure of the hematoxylin, the fluorescence intensity of hematoxylin peripheral substituted phthalocyanine decreased compared with free substituted phthalocyanines. The fluorescence lifetimes of axially substituted phthalocyanine was fitted to be 3.613 ns. This compound may be considered as a promising photosensitizer for PDT.

  8. Localization Study of Co-Phthalocyanines in Cells by Raman Micro(spectro)scopy

    NARCIS (Netherlands)

    Arzhantsev, S.Y.; Arzhantsev, S.Y.; Chikishev, A.Y.; Chikishev, A.Y.; Koroteev, N.I.; Greve, Jan; Otto, Cornelis; Sijtsema, N.M.

    1999-01-01

    An investigation of intracellular localization of Co-phthalocyanines is reported. The Raman images of K562 cells stained with phthalocyanine were acquired. To understand the peculiarities of the Raman images, measurements were performed at different z-axis positions. The intracellular concentration

  9. Localization study of Co-phthalocyanines in cells by Raman micro(spectro)scopy

    NARCIS (Netherlands)

    Arzhantsev, S Y; Chikishev, A Y; Koroteev, N I; Greve, J; Otto, C; Sijtsema, N M

    An investigation of intracellular localization of Co-phthalocyanines is reported. The Raman images of K562 cells stained with phthalocyanine were acquired. To understand the peculiarities of the Raman images, measurements were performed at different z-axis positions. The intracellular concentration

  10. XPS investigation of thionyl chloride action on iron phthalocyanines and naphthalocyanines and on hydrogen phthalocyanine — Correlations with the activity of Li/SOCl 2 cells

    Science.gov (United States)

    Savy, Michel; Riga, Joseph; Verbist, Jacques J.

    1989-03-01

    X-ray photoelectron spectroscopic measurements have been performed on iron phthalocyanines and naphthalocyanines, and hydrogen phthalocyanine powders, after dissolution in SOCl 2 and reprecipitation. The comparison of XPS results with catalytic activities observed in the lithium/thionyl chloride batteries during their discharge underlines the rôles of the central ion oxidation facility and ligand stability in the electrocatalysis of SOCl 2 reduction.

  11. MCM-41介孔分子筛中负载酞菁配合物的研究%Study of Metal-phthalocyanine Encapsulated in Mesoporous Molecular Sieves MCM-41

    Institute of Scientific and Technical Information of China (English)

    崔子祥; 薛永强; 李萍

    2012-01-01

    Zn-phthalocyanine complex(Ⅱ), which periphery has substituents was synthesized, and encapsulated in mesoporous molecular sieves MCM-41. The prepared samples was characterized by FT-1R, UV-vis-Nir, XRD, FESEM, TEM and N2 adsorption-desorption instrument. The research shows that the prepared phthalocyanine copper zinc can be encapsulated in mesoporous molecular sieves MCM-41 in the form of monomer and dipolymer. The prepared phthalocyanine zinc with high concentration encapsulated in MCM-41 is in favour of preparing mesoporous molecular sieves samples with higher crystallinity and pore canal order.%合成了Zn-酞菁化合物,通过水热法将酞菁化合物负载在MCM-41介孔分子筛中.利用FT-IR、UV-vis-Nir、XRD、FESEM、TEM及N2吸附-脱附仪对酞菁负载后的样品进行了表征.研究结果表明:较高浓度Zn-酞菁能够负载到介孔分子筛中,并且随着酞菁配合物浓度的增加,介孔分子筛孔道的有序性及结晶度都提高.

  12. Structural study of monolayer cobalt phthalocyanine adsorbed on graphite

    CERN Document Server

    Scheffler, M; Baumann, D; Schlegel, R; Hänke, T; Toader, M; Büchner, B; Hietschold, M; Hess, C

    2014-01-01

    We present microscopic investigations on the two-dimensional arrangement of cobalt phthalocyanine molecules on a graphite (HOPG) substrate in the low coverage regime. The initial growth and ordering of molecular layers is revealed in high resolution scanning tunneling microscopy (STM). On low coverages single molecules orient mostly along one of the substrate lattice directions, while they form chains at slightly higher coverage. Structures with two different unit cells can be found from the first monolayer on. A theoretical model based on potential energy calculations is presented, which relates the two phases to the driving ordering forces.

  13. Magnetic interaction in oxygenated alpha Fe-phthalocyanines

    Energy Technology Data Exchange (ETDEWEB)

    Kuzmann, Ernő, E-mail: kuzmann@caesar.elte.hu; Homonnay, Zoltán; Horváth, Attila [Institute of Chemistry, Eötvös Loránd University, P.O. Box 32, 1512 Budapest (Hungary); Pechousek, Jiri; Cuda, Jan; Machala, Libor; Zoppellaro, Giorgio; Zboril, Radek [Regional Centre of Advanced Technologies and Materials, Departments of Experimental Physics and Physical Chemistry, Faculty of Science Palacky University, 17. Listopadu 1192/12, 771 46 Olomouc (Czech Republic); Yin, Houping; Wei, Yen [Department of Chemistry, Drexel University, Philadelphia, PA 19104 (United States); Klencsár, Zoltán [Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, 1117 (Hungary); Kubuki, Shiro [Department of Chemistry, Graduate School of Science and Engineering, Tokyo Metropolitan University, 1-1 Minami-Osawa, Hachi-Oji, Tokyo 192-0397 (Japan); Nath, Amar [Department of Chemistry, University of North Carolina, Asheville, NC 28804 (United States)

    2014-10-27

    Alpha iron phthalocyanines (α-FePc) oxygenated at low temperatures were investigated with the help of {sup 57}Fe Mössbauer spectroscopy, magnetization measurements (SQUID) and X-ray diffractometry (XRD). Mössbauer spectroscopy revealed that upon oxygenation of α-FePc, new species were formed which could be associated with Fe{sup III}Pc oxygen adducts. Unexpectedly, magnetically split spectrum of oxygenated α-FePc was observed below 20 K. In-field Mössbauer spectra in a 5 T external magnetic field at 5K and magnetization measurements indicate antiferromagnetic coupling in oxygenated α-FePc.

  14. Photoconductivity study of acid on Zinc phthalocyanine pyridine thin films

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Sukhwinder, E-mail: ss7667@gmail.com [Department of Physics, Govt. College for Girls, Ludhiana (India); Saini, G. S. S.; Tripathi, S. K. [Department of Physics, Panjab University, Chandigarh (India)

    2016-05-06

    The Metal Phthalocyanine (MPc) have attracted much interest because of chemical and high thermal stability. Molecules forming a crystal of MPc are held together by weak attractive Vander Waals forces. Organic semiconductors have π conjugate bonds which allow electrons to move via π-electron cloud overlaps. Conduction mechanisms for organic semiconductor are mainly through tunneling; hopping between localized states, mobility gaps, and phonon assisted hopping. The photo conductivity of thin films of these complexes changes when exposed to oxidizing and reducing gases. Arrhenius plot is used to find the thermal activation energy in the intrinsic region and impurity scattering region. Arrhenius plotsare used to find the thermal activation energy.

  15. Novel phthalocyanine thin film for compact disc recordable

    Institute of Scientific and Technical Information of China (English)

    Yongyou Geng(耿永友); Donghong Gu(顾冬红); Yiqun Wu(吴谊群); Fuxi Gan(干福熹)

    2003-01-01

    In this paper, the spin-coated thin films of phthalocyanine dye are presented. Absorption spectrum ofthe thin film shows a comparatively broad absorption in the wavelength range 630 - 770 nm. Opticalparameters of the thin film were measured by a spectroscopic ellipsometer system. 5-in CD-R discs madeof this dye exhibit good performance with Yamaha 20-speed recorder. Jitters of land and pit are less than30 ns, and the 3T-11T's signals show very good quality. This dye is a promising recording medium forCD-R with much higher recording speed.

  16. Phthalocyanine-Carbon Nanostructure Materials Assembled through Supramolecular Interactions.

    Science.gov (United States)

    Bottari, Giovanni; Suanzes, Juan A; Trukhina, Olga; Torres, Tomas

    2011-04-21

    The use of self-assembly for the construction of materials based on phthalocyanines and carbon nanostructures-fullerenes, single-walled carbon nanotubes, and graphene-has demonstrated to be a versatile strategy for the preparation of novel, multifunctional systems. Photophysical studies carried out on these photo- and electroactive supramolecular ensembles have revealed the occurrence of an efficient photoinduced electron-transfer process, thus paving the way for the utilization of these materials as active components in optoelectronic devices. This Perspective highlights the recent progress in the preparation of such materials and the potential use of these systems for the construction of nanostructured materials with singular physicochemical properties.

  17. The fluorescence and dynamics properties in phenoxy-phthalocyanines liquid

    Science.gov (United States)

    Yao, Cheng-Bao; Yan, Xiao-Yan; Tan, Ming-Yue; Li, Jin; Sun, Wen-Jun; Yang, Shou-Bin

    2015-06-01

    We investigated the one/two-photon fluorescence and excited state dynamics properties of two synthesized phenoxy-phthalocyanines (Pc1 and Pc2) using mild reaction coordination method. The results show that the fast decay component in the time-resolved fluorescence technique dynamics comes from the intramolecular vibrational relaxation, the slower ones from the internal conversion. Furthermore, in comparison with one-photon fluorescence spectra, the red shift of two-photon fluorescence spectra can be explained by the reabsorption effect of molecules. The samples are expected to be a potential candidate for optical applications and photodynamic therapy.

  18. Magnetism and multiplets in metal-phthalocyanine molecules.

    Science.gov (United States)

    Kitaoka, Y; Sakai, T; Nakamura, K; Akiyama, T; Ito, T

    2013-05-07

    Magnetism and multiplets for metal-phthalocyanine (MPc) molecules with transition-metals (M) of Mn and Co were investigated based on the constraint density functional theory calculations by imposing density matrix constraint on the d-orbital occupation numbers. For the MnPc, the ground state is found to be the (4)Eg state with the perpendicular magnetic anisotropy with respect to the molecular plane, while for the CoPc, the ground state is the (2)A1g state with a planar magnetic anisotropy.

  19. An application of the coincidence Doppler spectroscopy for substances of chemical interest: phthalocyanine and acetylacetonate complexes

    CERN Document Server

    Ito, Y

    2000-01-01

    Coincidence Doppler spectroscopy, which is particularly powerful when one is concerned with high momentum components of positron annihilation gamma-rays, has been applied to two different kinds of organo-metallic ligands: metal phthalocyanines and metal acetylacetonates. The energy (momentum) profiles of the annihilation gamma-rays were the same for metal phthalocyanines indicating that positron and/or positronium are not interacting with the metal ions. However, the profiles for the metal acetylacetonates evidently showed a dependence on the kind of metal ions. Discussion is made on the features of positron interaction which are different for phthalocyanines and acetylacetonates.

  20. Titanium and Ruthenium Phthalocyanines for NO2 Sensors: A Mini-Review

    Directory of Open Access Journals (Sweden)

    Valerio Rossi Albertini

    2009-07-01

    Full Text Available This review presents studies devoted to the description and comprehension of phenomena connected with the sensing behaviour towards NO2 of films of two phthalocyanines, titanium bis-phthalocyanine and ruthenium phthalocyanine. Spectroscopic, conductometric, and morphological features recorded during exposure to the gas are explained and the mechanisms of gas-molecule interaction are also elucidated. The review also shows how X-ray reflectivity can be a useful tool for monitoring morphological parameters such as thickness and roughness that are demonstrated to be sensitive variables for monitoring the exposure of thin films of sensor materials to NO2 gas.

  1. Spectroscopic insights on energy transfer phenomenon from phthalocyanine to gold nanoparticle and role of phthalocyanine-gold nanoparticle conjugate over supramolecular interaction between fullerene and phthalocyanine in solution

    Science.gov (United States)

    Ray, Anamika; Bhattacharya, Sumanta

    2016-05-01

    This letter envisages the photophysical insights on phthalocyanine (Pc)-gold nanoparticle (AuNp) conjugate in solution. Both steady state and time-resolved fluorescence studies evoke remarkable enhancement in energy transfer efficiency from ZnPc to AuNp in comparison to free-base Pc (H2Pc) in toluene. It is observed that in presence of AuNp, selectivity in binding for the non-covalent complex of H2Pc with PC70BM (a fullerene derivative) is found to be ∼3.0 times higher compared to ZnPc-PC70BM system. Dynamic light scattering, transmission electron microscope, atomic force microscope and fluorescence microscope measurements provide very good support in favour of the rationale behind Pc-AuNp interaction in solution.

  2. Copper nanoparticles encapsulated in multi-shell carbon cages

    Energy Technology Data Exchange (ETDEWEB)

    Schaper, A.K. [Material Sciences Center and Department of Geosciences, Philipps University, Hans-Meerwein-Str., 35032, Marburg (Germany); Hou, H. [Material Sciences Center and Department of Chemistry, Philipps University, Hans-Meerwein-Str., 35032, Marburg (Germany); University of Akron, Ohio (United States); Greiner, A. [Material Sciences Center and Department of Chemistry, Philipps University, Hans-Meerwein-Str., 35032, Marburg (Germany); Schneider, R. [Institute of Physics, Humboldt University, Invalidenstr. 110, 10115, Berlin (Germany); Phillipp, F. [Max Planck Institute for Metal Research, Heisenbergstr. 3, 70569, Stuttgart (Germany)

    2004-01-01

    Nanoparticles are attracting increasing interest because of their high potential for a great number of practical applications, such as optical and electronic devices, nanoscale storage, and delivery systems. Using Cu-phthalocyanine as precursor material, we have synthesized multi-shell graphitic carbon nanospheres without and with metal encapsulation, depending on the pyrolysis conditions. The encapsulated elemental copper nanocrystals achieved using that route were of the order of 50 nm in size. The particles were characterized in detail by high-resolution transmission electron microscopy (HRTEM) and by energy filtering microscopy (EFTEM). The concentric graphitic carbon shells of the as-grown particles were clearly discernable. After in situ high-temperature annealing, an increase in the degree of order was observed. Under high-voltage electron irradiation and heating, a melting point reduction of the enclosed nanosized copper of more than 200 K could be detected, as compared to the melting point 1083 C of bulk copper. Time-resolved imaging revealed the displacement of the melting copper by migration through the carbon shells, leaving intact carbon cages with a central hole. At intermediate stages of this process the transformation into a hexagonal morphology of the copper nanocrystals was observed. (orig.)

  3. Photocatalytic degradation of atrazine by porphyrin and phthalocyanine complexes.

    Science.gov (United States)

    Héquet, V; Le Cloirec, P; Gonzalez, C; Meunier, B

    2000-08-01

    This study principally focused on a new kind of photochemical reaction catalyst: porphyrin and phthalocyanine complexes. In a first step, the preparation of the catalysts was optimized. A resin has been chosen to be the support of the complexes. Efficiency of catalytic activity is performed on the degradation of a pesticide: atrazine. The best atrazine degradation occurs with 4.6% of complexes versus substrate. The role of the surface has also been shown to be important. Then, their performances were demonstrated in terms of kinetics and degradation routes, compared to a classical catalyst: titanium dioxide. This study seeks to assess the efficiency of these systems both in a mercury lamp reactor and under solar irradiation which reduces energy costs. The best atrazine degradation half-life found for the complexes is about 200 min with the iron phthalocyanine. These catalysts exhibit particular oxidation activities. Indeed, the degradation routes have been found different between the semi-conductor and the metallic complexes. These complexes are able to cleave the triazinic ring more efficiently than the titanium dioxide.

  4. A Novel Gas Sensor Transducer Based on Phthalocyanine Heterojunction Devices

    Directory of Open Access Journals (Sweden)

    Marcel Bouvet

    2007-11-01

    Full Text Available Experimental data concerning the changes in the current-voltage (I-V perfor-mances of a molecular material-based heterojunction consisting of hexadecafluorinatednickel phthalocyanine (Ni(F16Pc and nickel phthalocyanine (NiPc,(Au|Ni(F16Pc|NiPc|Al are introduced as an unprecedented principle of transduction for gassensing performances. The respective n- and p-type doped-insulator behaviors of therespective materials are supported, owing to the observed changes in surface potential(using the Kelvin probe method after submission to electron donor (ammonia and electronacceptor gases (ozone. On the other hand, the bilayer device exhibits strong variations inthe built-in potential of the junction and in its rectification ratio. Moreover, large increasesoccur in forward and reverse currents in presence of ammonia vapors. These make possiblea multimodal principle of detection controlled by a combined effect between theheterojunction and the NiPc|Al contact. Indeed, this metal/organic junction plays a criticalrole regarding the steady asymmetry of the I-V profiles during the device’s doping evenusing high ammonia concentrations. This approach offers a more sophisticated alternative tothe classically studied, but at times rather operation-limited, resistive gas sensors.

  5. Asymmetric Zinc Phthalocyanines as Dye-Sensitized Solar Cells

    Science.gov (United States)

    Tunc, Gulenay; Yavuz, Yunus; Gurek, Aysegul; Canimkurbey, Betul; Kosemen, Arif; San, Sait Eren; Ahsen, Vefa

    Dye-sensitized solar cells (DSSCs) have received increasing attention due to their high incident to photon efficiency, easy fabrication and low production cost . Tremendous research efforts have been devoted to the development of new and efficient sensitizers suitable for practical use. In TiO2-based DSSCs, efficiencies of up to 11.4% under simulated sunlight have been obtained with rutheniumepolypyridyl complexes. However, the main drawback of ruthenium complexes is the lack of absorption in the red region of the visible light and the high cost. For this reason, dyes with large and stable p-conjugated systems such as porphyrins and phthalocyanines are important classes of potential sensitizers for highly efficient DSSCs. Phthalocyanines (Pcs) have been widely used as sensitizers because of their improved light-harvesting properties in the far red- and near-IR spectral regions and their extraordinary robustness [1]. In this work, a series of asymmetric Zn(II) Pcs bearing a carboxylic acid group and six hexylthia groups either at the peripheral or non-peripheral positions have been designed and synthesized to investigate the influence of the COOH group and the positions of hexylthia groups on the dye-sensitized solar cell (DSSC) performance.

  6. Different assemblies of a phthalocyanine derivative on metal surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Samuely, Tomas; Stoehr, Meike [Institut fuer Physik,Universitaet Basel, Schweiz (Switzerland); Jung, Thomas [Paul Scherrer Institut, Villigen, Schweiz (Switzerland); Haas, Marco; Liu, Shi-Xia; Decurtins, Silvio [Departement fuer Chemie und Biochemie, Universitaet Bern, Schweiz (Switzerland)

    2007-07-01

    Phthalocyanines have been the subject of intense studies due to their wide range of optical, structural and electronic properties arising from their large {pi}-conjugated system and their assembling into co faciallystacked arrays. We studied a phthalocyanine derivative which features eight ditertiarybutylphenyl substituents attached over an oxygen atom to the peripheral phenyl rings. Ordered assemblies of the derivative were prepared by thermal evaporation, whereas Ag(111) and Au(111) were used as substrates, respectively. The investigations were carried out by means of STM at various temperatures. For coverage less than one monolayer, two different assemblies were observed. At room temperature, a mobile phase was detected next to the ordered islands. Increasing the coverage results in only one ordered phase, while the second layer begins to form before a full monolayer is completed. Applying different bias voltages had a vast effect on the appearance of the imaged molecules. The assembled domains of the derivative could be suitable for subsequent deposition of various molecules: complexes with interesting magnetic, electronic, redox or photo-active properties could be formed.

  7. Photochemical and Photophysical Properties of Phthalocyanines Modified with Optically Active Alcohols

    Directory of Open Access Journals (Sweden)

    Aline A. Ramos

    2015-07-01

    Full Text Available Three phthalocyanine derivatives were synthesized and characterized: one modified with a racemic mixture of 1-(4-bromophenylethanol and two other macrocycles modified with each one of the enantioenriched isomers (R-1-(4-bromophenylethanol and (S-1-(4-bromophenylethanol. The compounds were characterized by 1H-NMR spectroscopy, mass spectrometry, UV-Vis absorption, and excitation and emission spectra. Additionally, partition coefficient values and the quantum yield of the generation of oxygen reactive species were determined. Interestingly, the phthalocyanine containing a (R-1-(4-bromophenylethoxy moiety showed higher quantum yield of reactive oxygen species generation than other compounds under the same conditions. In addition, the obtained fluorescence microscopy and cell viability results have shown that these phthalocyanines have different interactions with mammary MCF-7 cells. Therefore, our results indicate that the photochemical and biological properties of phthalocyanines with chiral ligands should be evaluated separately for each enantiomeric species.

  8. Photophysical, Photochemical, and BQ Quenching Properties of Zinc Phthalocyanines with Fused or Interrupted Extended Conjugation

    Directory of Open Access Journals (Sweden)

    Gülşah Gümrükçü

    2014-01-01

    Full Text Available The effects of substituents and solvents on the photophysical and photochemical parameters of zinc(II phthalocyanines containing four Schiff’s base substituents attached directly and through phenyleneoxy-bridges on peripheral positions are reported. The group effects on peripheral position and the continual and intermittent conjugation of the phthalocyanine molecules on the photophysical and photochemical properties are also investigated. General trends are described for photodegradation, singlet oxygen, and fluorescence quantum yields of these compounds in dimethylsulfoxide (DMSO, dimethylformamide (DMF, and tetrahydrofurane (THF. Among the different substituents, phthalocyanines with cinnamaldimine moieties (1c and 2c have the highest singlet oxygen quantum yields (ΦΔ and those with nitro groups (1a and 2a have the highest fluorescence quantum yields in all the solvents used. The fluorescence of the substituted zinc(II phthalocyanine complexes is effectively quenched by 1,4-benzoquinone (BQ in these solvents.

  9. Nonlinear optical response of tetra and mono substituted zinc phthalocyanine complexes

    Energy Technology Data Exchange (ETDEWEB)

    Fashina, Adedayo; Nyokong, Tebello, E-mail: t.nyokong@ru.ac.za

    2015-11-15

    The nonlinear absorption properties of 6 mono-substituted and 3 symmetric zinc phthalocyanine complexes have been studied in dimethylsulfoxide (DMSO) using 10 ns pulses at 532 nm. The non linear absorption of the complexes has been studied using the Z-scan technique. The study showed that both the singlet and triplet excited states contribute to the non linear absorption behavior. The nonlinear third-order susceptibility and second-order hyperpolarizability values of the complexes are reported. It was observed that two of the symmetric phthalocyanine complexes (5-α substituted with aminophenoxy and 9-β substituted with carboxyphenoxy) showed better and promising optical nonlinearity when compared to the other complexes studied. - Highlights: • Nonlinear absorption properties of zinc phthalocyanine are reported • Singlet and triplet excited states contribute to the non linear absorption. • Symmetrically tetra substituted phthalocyanines showed better optical nonlinearity.

  10. The effect of axial ligands on the quantum yield of singlet oxygen of new silicon phthalocyanine

    Science.gov (United States)

    Lv, Huafei; Zhang, Xuemei; Yu, Xinxin; Pan, Sujuan; Xie, Shusen; Yang, Hongqin; Peng, Yiru

    2016-10-01

    The singlet oxygen (1O2) production abilitity is an important factor to assess their potential as effective of photosensitizers. In this paper, the 1O2 production rate, production rate constant and quantum yield of silicon(IV) phthalocyanine axially bearing 1-3 generation dendritic substituents were evaluated by a high performance liquid chromatographic method. The results show that the 1O2 production rate and production rate constant of these compounds increase gradually with dendritic generations increase. And the 1O2 quantum yield of silicon(IV) phthalocyanine with first generation dendritic ligand was the highest. This may be due to the isolation effect of the dendritic ligands on the phthalocyanine core. The parameters of the observed 1O2 production properties will provide valuable data for these dendrimer phthalocyanines as promising photosensitizer in PDT application.

  11. A novel fully conjugated phenanthroline-appended phthalocyanine: synthesis and characterisation.

    Science.gov (United States)

    Rusanova, Julia; Pilkington, Melanie; Decurtins, Silvio

    2002-10-07

    The synthetic route to a new fully conjugated phenanthroline appended phthalocyanine is described. This compound has been fully characterised by elemental analysis, UV-VIS, IR, MS and 1H NMR spectroscopy.

  12. Theoretical investigation of the electronic structure of a substituted nickel phthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Kaur, Prabhjot, E-mail: prabhphysics@gmail.com; Sachdeva, Ritika [Department of Physics, Panjab University Chandigarh-160014, Chandigarh (India); Singh, Sukhwinder [Department of Physics, Govt. College for Girls, Ludhiana-141008, Ludhiana (India)

    2016-05-23

    The optimized geometry and electronic structure of an organic compound nickel phthalocyanine tetrasulfonic acid tetra sodium salt have been investigated using density functional theory. We have also optimized the structure of nickel phthalocyanine tetrasulfonic acid tetra sodium salt in dimethyl sulfoxide to study effects of solvent on the electronic structure and transitions. Experimentally, the electronic transitions have been studied using UV-VIS spectroscopic technique. It is observed that the electronic transitions obtained from the theoretical studies generally agree with the experiment.

  13. A study of single-walled carbon nanotubes modified by organics of the phthalocyanine category

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Organics of the phthalocyanine category have very good nonlinear optical properties. The single-walled carbon nanotubes were modified by using the phenoxy phthalocyanine. Characterization analysis was made by means of the transmission electron microscope (TEM), ultraviolet visible absorptive spectra, fluorescent spectra and Raman spectra. Under the TEM, it was observed that the composite looked like sugarcoated haws. By comparing the ultraviolet visible absorptive spectra before and after absorption, it was...

  14. An investigation on linear and non-linear optical constants of nano-spherical CuPc thin films for optoelectronic applications

    Energy Technology Data Exchange (ETDEWEB)

    Yahia, I.S. [Nano-Science & Semiconductor Labs, Metallurgical Lab., Department of Physics, Faculty of Education, Ain Shams University, Roxy, Cairo (Egypt); Advanced Functional Materials & Optoelectronic Laboratory (AFMOL), Department of Physics, Faculty of Science, King Khalid University, P.O. Box 9004, Abha (Saudi Arabia); Ganesh, V. [Advanced Functional Materials & Optoelectronic Laboratory (AFMOL), Department of Physics, Faculty of Science, King Khalid University, P.O. Box 9004, Abha (Saudi Arabia); Shkir, M., E-mail: shkirphysics@gmail.com [Advanced Functional Materials & Optoelectronic Laboratory (AFMOL), Department of Physics, Faculty of Science, King Khalid University, P.O. Box 9004, Abha (Saudi Arabia); AlFaify, S. [Advanced Functional Materials & Optoelectronic Laboratory (AFMOL), Department of Physics, Faculty of Science, King Khalid University, P.O. Box 9004, Abha (Saudi Arabia); Zahran, H.Y. [Nano-Science & Semiconductor Labs, Metallurgical Lab., Department of Physics, Faculty of Education, Ain Shams University, Roxy, Cairo (Egypt); Advanced Functional Materials & Optoelectronic Laboratory (AFMOL), Department of Physics, Faculty of Science, King Khalid University, P.O. Box 9004, Abha (Saudi Arabia); Algarni, H. [Advanced Functional Materials & Optoelectronic Laboratory (AFMOL), Department of Physics, Faculty of Science, King Khalid University, P.O. Box 9004, Abha (Saudi Arabia); Abutalib, M.M.; Al-Ghamdi, Attieh A. [Centre of Nanotechnology, Physics Department-Faculty of Science-AL Faisaliah Campus, King Abdulaziz University, Jeddah (Saudi Arabia); El-Naggar, A.M.; AlBassam, A.M. [Research Chair of Exploitation of Renewable Energy Applications in Saudi Arabia, Physics & Astronomy Dept., College of Science, King Saud University, P.O. Box 2455, Riyadh 11451 (Saudi Arabia)

    2016-09-01

    In the current work, the authors present the systematic study on linear and nonlinear optical properties of Copper-phathalocyanine thin film deposited by thermal evaporation system for the first time. The thickness of the prepared thin film was measured and found to be ~300 nm. X-ray diffraction and AFM study confirms that the prepared thin film possess good quality. The orientation of the grown thin film is found to be along (100). UV–vis-NIR study shows that the deposited thin film is highly transparent (>80%) in the wavelength range of 700–2500 nm. Further, the recorded optical data was used to determine the various linear and nonlinear optical parameters. The calculated value of refractive index is found to be in the range of 0.4–1.0. The direct and indirect band gap value is found to be 2.9 and 3.25 eV, respectively. The value of linear and nonlinear susceptibilities is found to be in order of 10{sup −12}. The higher value of linear and nonlinear parameters makes it suitable for optoelectronic applications.

  15. Mesomorphism and Optical Properties of Peripherally Substituted Phthalocyanines: Influence of Chain Length, Linking Group and Central Metal Ion

    OpenAIRE

    Sleven, Jurgen

    2002-01-01

    Phthalocyanines form a colourful class of macrocyclic compounds, attracting the attention of many scientists. Some of these compounds – especially the metal containing phthalocyanines – play an important role in industrial activity and in society. Applications for phthalocyanines are found in the fields of non-linear optics, catalysis, electronic (bio)sensors, photovoltaic solar cells, optical data storage, lubricants, photo- and radiosensitizers for treatment of cancer, protein inhibitors … ...

  16. Photophysical property of a polymeric nanoparticle loaded with an aryl benzyl ester silicon (IV) phthalocyanine

    Science.gov (United States)

    Pan, Sujuan; Ma, Dongdong; Chen, Xiuqin; Wang, Yuhua; Yang, Hongqin; Peng, Yiru

    2014-09-01

    Because of their excellent near-infrared (NIR) optical properties, phthalocyanines (Pcs) have been regarded as promising therapy agents for fluorescence image-guided drug delivery and noninvasive treatment of tumors by photodynamic therapy (PDT). Nevertheless, phthalocyanines are substantially limited in clinical applications owing to their poor solubility, aggregation and insufficient selectivity for cancer cells. To address these issues, we have developed a novel dendrimer-based theranostic nanoparticle for tumor-targeted delivery of phthalocyanine. The preparation procedure involved the modification of the silicon (IV) phthalocyanine molecule with a dendritic axially substitution, which significantly enhances their photophysical property. In order to improve biocompatibility and tumor-targeted delivery, the hydrophobic dendritic phthalocyanine was encapsulated by diblock amphiphilic copolymer poly (ethylene glycol)-poly (Epsilon-caprolactone) (MPEG-PCL) to form a polymeric nanoparticle. The polymeric nanoparticle is spherical with a diameter at about 90 nm. The photophysical property of the polymeric nanoparticle was studied by UV/Vis and fluorescence spectroscopic methods. Compared with the free dendritic phthalocyanine, the Q band of the polymeric nanoparticle was red-shifted, and the fluorescence intensity decreased. Furthermore, the polymeric nanoparticle has a relatively high loading amount and encapsulation rate. Therefore, the polymeric nanoparticle would be a promising third-generation photosensitizer (PS) for PDT.

  17. Photophysical property of the pyridyl and pyrimidinyloxy silicon (IV) phthalocyanines and their morphology of polymeric nanoparticles

    Science.gov (United States)

    Pan, Sujuan; Chen, Zhe; Wu, Shijun; Jiang, Yufeng; Zeng, Di; Wang, Yuhua; Yang, Hongqin; Peng, Yiru

    2016-10-01

    Phthalocyanines (Pcs) are extensively studied by many scientists because of their interesting optical, electrical properties, and good thermal stability. The unsubstituted Pcs can present solubility and aggregation behaviour problems for their limiting applications. In our study two pyridyl and pyrimidinyloxy silicon (IV) phthalocyanines were synthesized. Their photophysical properties were examined by UV-Vis, steady-state and time-resolved fluorescence spectroscopic methods. The positions of Q band were observed at 670 nm for two phthalocyanines. Compared with silicon phthalocyanine dichloride (SiPcCl2), the fluorescence intensities and lifetimes of pyridyl and pyrimidinyloxy silicon (IV) phthalocyanines increased. In order to improve biocompatibility and tumor-targeted delivery, the hydrophobic dendritic phthalocyanine were encapsulated by diblock amphiphilic copolymer poly (N'-benzyl oxygen carbonyl lysine)-poly (ethylene glycol)-poly (N'-benzyl oxygen carbonyl lysine) (PLL(Z)-PEG-PLL(Z)) to form the polymeric nanoparticles. The morphology of two nanoparticles were investigated by using atomic force microscope. The polymeric nanoparticles were spherical with the diameter at about 35 nm. The polymeric nanoparticle SiPc(OR2)2@PLL(Z)-PEG-PLL(Z) would be the promising third-generation photosensitizer (PS) for photodynamic therapy (PDT).

  18. Electrical Characteristics of Copper Phthalocyanine Thin-Film Transistors with Polyamide-6/Polytetrafluoroethylene Gate Insulator

    Institute of Scientific and Technical Information of China (English)

    YU Shun-Yang; XU Shi-Ai; MA Dong-Ge

    2007-01-01

    Polyamide-6(PA 6)/polytetrafluoroethylene is studied as a potential gate dielectric for flexible organic thin film transistors.The salne method used for the formation of organic semiconductor and gate dielectric films greatly simplifies the fabrication process of devices.The fabricated transistors show good electrical characteristics.Ambipolar behaviour is observed even when the device is operated in air.

  19. Studying the operation characteristics and structure of vertical channel copper-phthalocyanine organic semiconductor transistor

    Institute of Scientific and Technical Information of China (English)

    ZHU Min; SONG Ming-xin; GUI Tai-long; WANG Xuan; YIN Jing-hua; WANG Dong-xing; ZHAO Hong

    2005-01-01

    The creation of Au/CuPc/Al/CuPc/structure is a perpendicular type electricity found in the channel of organic static induction transistor. In the following we analyze transistor operation characteristics and machine structural relation. The results express that the transistor drives the voltage low and has no-saturation currentvoltage characteristics. Its operation characteristics are dependant on gate bias voltage and the construction of the aluminum electrode.The vertical channel of organic static induction transistor (OSIT) , with structure of Au/CuPc/Al/CuPc/Cu, has been determined. According to the test results, the relation of its operation characteristics and device structure was analyzed. The results show that this transistor has a low driving voltage and unsaturation Ⅰ-Ⅴ characteristics. Its operation characteristics are dependant on gate bias voltage and the structure of the aluminum electrode.

  20. Regiospecific synthesis of tetrasubstituted phthalocyanines and their liquid crystalline order.

    Science.gov (United States)

    Apostol, Petru; Bentaleb, Ahmed; Rajaoarivelo, Mbolotiana; Clérac, Rodolphe; Bock, Harald

    2015-03-28

    Metal-free and metal(II) all-endo-tetraalkoxy-phthalocyanines of C4h symmetry are synthesised regiospecifically from 3-(2-butyloctyloxy)phthalonitrile with lithium octanolate and subsequent metal ion exchange. The voluminous, yet not overly large, and racemically disordered alkoxy substituent not only renders the cyclotetramerisation regiospecific, but also leads to liquid crystalline self-assembly with attainable clearing temperatures and persisting columnar organisation at room temperature. A rare hexagonal mesophase with twelve columns per hexagonal unit cell is found in the metal-free homologue, whereas the metal complexes show rectangular mesophases. The clearing temperature increases with increasing axial component of the metal ion coordination sphere. At low temperature, significant antiferromagnetic exchange between magnetic centres is observed for the Co(II) homologue, whereas the magnetic centres are magnetically independent in the Cu(II) derivative, in line with the observed higher clearing temperature in the Co(II) case that testifies of stronger interdisk interactions.

  1. Giant ferromagnetic π -d interaction in a phthalocyanine molecule

    Science.gov (United States)

    Murakawa, H.; Kanda, A.; Ikeda, M.; Matsuda, M.; Hanasaki, N.

    2015-08-01

    We experimentally demonstrate that the ferromagnetic intramolecular π -d interaction works between an itinerant π -electron spin and a localized d -electron's magnetic moment in the iron-phthalocyanine (Pc) molecular compound. The evaluation of the hidden π -d coupling is achieved by preparing the isolated Fe(Pc )(CN ) 2 molecular solution with unpaired π - and d -electron spins, which is generated through the oxidization by iodine bromide (IBr). The monotonic increase of the magnetization with IBr addition and the saturation value of the Curie constant indicate the ferromagnetic π -d coupling. Furthermore, through the magnetization measurements of the single crystals of neutral π radical Fe(Pc )(CN ) 2.2 CHCl3 , we reveal that the on-site π -d interaction in Fe(Pc )(CN ) 2 is extremely large (Jπ d/kB>500 K ) among those in other molecular materials.

  2. Sensing Properties of Cobalt-Phthalocyanine-Based Multipurpose Sensor

    Science.gov (United States)

    Wahab, Fazal; Sayyad, M. H.; Khan, Dil Nawaz; Tahir, Muhammad; Aziz, Fakhra; Khan, Rashid; Karimov, Kh. S.

    2017-04-01

    Cobalt phthalocyanine (CoPc), an organic semiconductor, has been introduced as an active sensing layer in a surface-type multipurpose sensor owing to its stability, low fabrication cost, and multifunctional sensitivity. The capacitance of the sensor was recorded to increase 26.7-fold for a change in relative humidity (RH) from 0% to 92.3%, 12.6-fold for a change in illumination from 11.5 lx to 23,000 lx, and 5.2-fold for a change in temperature from 27°C to 187°C. The morphology of the active thin film of the sensor was analyzed by atomic force microscopy, revealing a rough surface favorable for moisture absorption and light harvesting. The CoPc film was amorphous in nature according to x-ray diffraction analysis. By virtue of its response to humidity, light, and temperature, this represents an attractive approach for cost-effective environmental sensing applications.

  3. Like a Bolt from the Blue: Phthalocyanines in Biomedical Optics

    Directory of Open Access Journals (Sweden)

    Norbert Lange

    2011-12-01

    Full Text Available The purpose of this review is to compile preclinical and clinical results on phthalocyanines (Pcs as photosensitizers (PS for Photodynamic Therapy (PDT and contrast agents for fluorescence imaging. Indeed, Pcs are excellent candidates in these fields due to their strong absorbance in the NIR region and high chemical and photo-stability. In particular, this is mostly relevant for their in vivo activation in deeper tissular regions. However, most Pcs present two major limitations, i.e., a strong tendency to aggregate and a low water-solubility. In order to overcome these issues, both chemical tuning and pharmaceutical formulation combined with tumor targeting strategies were applied. These aspects will be developed in this review for the most extensively studied Pcs during the last 25 years, i.e., aluminium-, zinc- and silicon-based Pcs.

  4. Like a bolt from the blue: phthalocyanines in biomedical optics.

    Science.gov (United States)

    Sekkat, Nawal; van den Bergh, Hubert; Nyokong, Tebello; Lange, Norbert

    2011-12-23

    The purpose of this review is to compile preclinical and clinical results on phthalocyanines (Pcs) as photosensitizers (PS) for Photodynamic Therapy (PDT) and contrast agents for fluorescence imaging. Indeed, Pcs are excellent candidates in these fields due to their strong absorbance in the NIR region and high chemical and photo-stability. In particular, this is mostly relevant for their in vivo activation in deeper tissular regions. However, most Pcs present two major limitations, i.e., a strong tendency to aggregate and a low water-solubility. In order to overcome these issues, both chemical tuning and pharmaceutical formulation combined with tumor targeting strategies were applied. These aspects will be developed in this review for the most extensively studied Pcs during the last 25 years, i.e., aluminium-, zinc- and silicon-based Pcs.

  5. An effective zinc phthalocyanine derivative for photodynamic antimicrobial chemotherapy

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Zhuo, E-mail: zchen@fjirsm.ac.cn [State Key Laboratory of Structural Chemistry and Danish-Chinese Centre for Proteases and Cancer, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Zhou, Shanyong; Chen, Jincan [State Key Laboratory of Structural Chemistry and Danish-Chinese Centre for Proteases and Cancer, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Li, Linsen [Department of Biochemistry, Shenyang Medical College, Shenyang, Liaoning 110034 (China); Hu, Ping; Chen, Song [State Key Laboratory of Structural Chemistry and Danish-Chinese Centre for Proteases and Cancer, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Huang, Mingdong, E-mail: mhuang@fjirsm.ac.cn [State Key Laboratory of Structural Chemistry and Danish-Chinese Centre for Proteases and Cancer, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China)

    2014-08-01

    Bacterial infection is a common clinical problem. The emergence of antibiotic resistant bacteria posts a severe challenge to medical practice worldwide. Photodynamic antimicrobial chemotherapy (PACT) uses laser light at specific wavelength to activate oxygen molecule in the human tissue into reactive oxygen species as antimicrobial agent. This activation of oxygen by laser light is mediated through a photosensitizer. Two key properties for potent photosensitizer are its absorbance of light in the infrared region (630–700 nm), which promotes tissue penetration depth, and the selective accumulation on bacteria instead of human tissue. We herein report a zinc phthalocyanine derivative, pentalysine β-carbonylphthalocyanine zinc (ZnPc-(Lys){sub 5}) and its antimicrobial effects in vitro and in an animal infection model. This photosensitizer has strong capability to kill bacteria at 670 nm. Chemically, it is a water-soluble and cationic photosensitizer carrying positive charge under physiological pH, and can specifically target to bacteria which usually bears negative charges on its surface. Compared with anionic ZnPc counterparts, ZnPc-(Lys){sub 5} shows a higher phototoxicity toward bacteria. PACT studies of ZnPc-(Lys){sub 5} in experimental infection animal model showed a significant bacteria inhibition compared to controls, and high selectivity of ZnPc-(Lys){sub 5} toward bacteria. These findings suggest ZnPc-(Lys){sub 5} is a promising antimicrobial photosensitizer for the treatment of infectious diseases. - Highlights: • Photodynamic antimicrobial chemotherapy (PACT) with water-soluble zinc phthalocyanine derivative offers a promising measure to deal with antibiotic resistance of bacteria. • The use of portable LED light sources that are battery-powered and with low cost may make possible the deployment of systems that can be used for wound decontamination. • ZnPc-(Lys){sub 5} is a potent photosensitizer for treatment of infectious diseases.

  6. Surface properties of self-assembled monolayer films of tetra-substituted cobalt, iron and manganese alkylthio phthalocyanine complexes

    Energy Technology Data Exchange (ETDEWEB)

    Akinbulu, Isaac Adebayo; Khene, Samson [Department of Chemistry, Rhodes University, Grahamstown 6140 (South Africa); Nyokong, Tebello, E-mail: t.nyokong@ru.ac.z [Department of Chemistry, Rhodes University, Grahamstown 6140 (South Africa)

    2010-09-30

    Self-assembled monolayer (SAM) films of iron (SAM-1), cobalt (SAM-2) and manganese (SAM-3) phthalocyanine complexes, tetra-substituted with diethylaminoethanethio at the non-peripheral positions, were formed on gold electrode in dimethylformamide (DMF). Electrochemical, impedimentary and surface properties of the SAM films were investigated. Cyclic voltammetry was used to investigate the electrochemical properties of the films. Ability of the films to inhibit common faradaic processes on bare gold surface (gold oxidation, solution redox chemistry of [Fe(H{sub 2}O){sub 6}]{sup 3+}/[Fe(H{sub 2}O){sub 6}]{sup 2+} and underpotential deposition (UDP) of copper) was investigated. Electrochemical impedance spectroscopy (EIS), using [Fe(CN){sub 6}]{sup 3-/4-} redox process as a probe, offered insights into the electrical properties of the films/electrode interfaces. Surface properties of the films were probed using atomic force microscopy (AFM) and scanning electron microscopy (SEM). The films were employed for the electrocatalytic oxidation of the pesticide, carbofuran. Electrocatalysis was evidenced from enhanced current signal and less positive oxidation potential of the pesticide on each film, relative to that observed on the bare gold electrode. Mechanism of electrocatalytic oxidation of the pesticide was studied using rotating disc electrode voltammetry.

  7. SYNTHESIS AND SUPRAMOLECULAR CHEMISTRY OF NOVEL LIQUID-CRYSTALLINE CROWN ETHER-SUBSTITUTED PHTHALOCYANINES - TOWARD MOLECULAR WIRES AND MOLECULAR IONOELECTRONICS

    NARCIS (Netherlands)

    VANNOSTRUM, CF; PICKEN, SJ; SCHOUTEN, AJ; NOLTE, RJM

    1995-01-01

    The synthesis of the metal-free and the dihydroxysilicon derivatives of tetrakis[4',5'-bis(decoxy)benzo-18-crown-6]phthalocyanine is described. The metal-free phthalocyanine is liquid crystalline and exhibits a crystalline phase to mesophase transition at 148 degrees C. The structures of the crystal

  8. Synthesis and Supramolecular Chemistry of Novel Liquid Crystalline Crown Ether-Substituted Phthalocyanines : Toward Molecular Wires and Molecular Ionoelectronics

    NARCIS (Netherlands)

    Nostrum, Cornelus F. van; Picken, Stephen J.; Schouten, Arend-Jan; Nolte, Roeland J.M.

    1995-01-01

    The synthesis of the metal-free and the dihydroxysilicon derivatives of tetrakis[4’,5’-bis(decoxy)benzo-18-crown-6]phthalocyanine is described. The metal-free phthalocyanine is liquid crystalline and exhibits a crystalline phase to mesophase transition at 148 °C. The structures of the crystalline ph

  9. Synthesis and Supramolecular Chemistry of Novel Liquid Crystalline Crown Ether-Substituted Phthalocyanines : Toward Molecular Wires and Molecular Ionoelectronics

    NARCIS (Netherlands)

    Nostrum, Cornelus F. van; Picken, Stephen J.; Schouten, Arend-Jan; Nolte, Roeland J.M.

    1995-01-01

    The synthesis of the metal-free and the dihydroxysilicon derivatives of tetrakis[4’,5’-bis(decoxy)benzo-18-crown-6]phthalocyanine is described. The metal-free phthalocyanine is liquid crystalline and exhibits a crystalline phase to mesophase transition at 148 °C. The structures of the crystalline

  10. Supramolecular Structure, Physical Properties, and Langmuir-Blodgett Film Formation of an Optically Active Liquid-Crystalline Phthalocyanine

    NARCIS (Netherlands)

    Nostrum, Cornelus F. van; Bosman, Anton W.; Gelinck, Gerwin H.; Schouten, Pieter G.; Warman, John M.; Devillers, Marinus A.C.; Meijerink, Andries; Picken, Stephen J.; Sohling, Ulrich; Schouten, Arend-Jan; Nolte, Roeland J.M.

    The structure and physical properties of optically active, metal-free 2,3,9,10,16,17,23,24-octa(S-3,7-dimethyloctoxy)phthalocyanine ((S)-Pc(8,2)) are reported and compared with those of the phthalocyanine with (R,S) side chains (mixture of 43 stereoisomers). Unlike the latter compound, (S)-Pc(8,2)

  11. Synthesis and Supramolecular Chemistry of Novel Liquid Crystalline Crown Ether-Substituted Phthalocyanines : Toward Molecular Wires and Molecular Ionoelectronics

    NARCIS (Netherlands)

    Nostrum, Cornelus F. van; Picken, Stephen J.; Schouten, Arend-Jan; Nolte, Roeland J.M.

    1995-01-01

    The synthesis of the metal-free and the dihydroxysilicon derivatives of tetrakis[4’,5’-bis(decoxy)benzo-18-crown-6]phthalocyanine is described. The metal-free phthalocyanine is liquid crystalline and exhibits a crystalline phase to mesophase transition at 148 °C. The structures of the crystalline ph

  12. SYNTHESIS AND SUPRAMOLECULAR CHEMISTRY OF NOVEL LIQUID-CRYSTALLINE CROWN ETHER-SUBSTITUTED PHTHALOCYANINES - TOWARD MOLECULAR WIRES AND MOLECULAR IONOELECTRONICS

    NARCIS (Netherlands)

    VANNOSTRUM, CF; PICKEN, SJ; SCHOUTEN, AJ; NOLTE, RJM

    1995-01-01

    The synthesis of the metal-free and the dihydroxysilicon derivatives of tetrakis[4',5'-bis(decoxy)benzo-18-crown-6]phthalocyanine is described. The metal-free phthalocyanine is liquid crystalline and exhibits a crystalline phase to mesophase transition at 148 degrees C. The structures of the crystal

  13. Antibacterial effect of cationic porphyrazines and anionic phthalocyanine and their interaction with plasmid DNA

    Science.gov (United States)

    Hassani, Leila; Hakimian, Fatemeh; Safaei, Elham; Fazeli, Zahra

    2013-11-01

    Resistance to antibiotics is a public health issue and identification of new antibacterial agents is one of the most important goals of pharmacological research. Among the novel developed antibacterial agents, porphyrin complexes and their derivatives are ideal candidates for use in medical applications. Phthalocyanines differ from porphyrins by having nitrogen atoms link the individual pyrrol units. The aza analogues of the phthalocyanines (azaPcs) such as tetramethylmetalloporphyrazines are heterocyclic Pc analogues. In this investigation, interaction of an anionic phthalocyanine (Cu(PcTs)) and two cationic tetrapyridinoporphyrazines including [Cu(2,3-tmtppa)]4+ and [Cu(3,4-tmtppa)]4+ complexes with plasmid DNA was studied using spectroscopic and gel electrophoresis methods. In addition, antibacterial effect of the complexes against Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria was investigated using dilution test method. The results indicated that both porphyrazines have significant antibacterial properties, but Cu(PcTs) has weak antibacterial effect. Compairing the binding of the phthalocyanine and the porphyrazines to DNA demonstrated that the interaction of cationic porphyrazines is stronger than the anionic phthalocyanine remarkably. The extent of hypochromicity and red shift of absorption spectra indicated preferential intercalation of the two porphyrazine into the base pairs of DNA helix. Gel electrophoresis result implied Cu(2,3-tmtppa) and Cu(3,4-tmtppa) are able to perform cleavage of the plasmid DNA. Consequently, DNA binding and cleavage might be one of the antibacterial mechanisms of the complexes.

  14. Elaboration of ammonia gas sensors based on electrodeposited polypyrrole--cobalt phthalocyanine hybrid films.

    Science.gov (United States)

    Patois, Tilia; Sanchez, Jean-Baptiste; Berger, Franck; Fievet, Patrick; Segut, Olivier; Moutarlier, Virginie; Bouvet, Marcel; Lakard, Boris

    2013-12-15

    The electrochemical incorporation of a sulfonated cobalt phthalocyanine (sCoPc) in conducting polypyrrole (PPy) was done, in the presence or absence of LiClO4, in order to use the resulting hybrid material for the sensing of ammonia. After electrochemical deposition, the morphological features and structural properties of polypyrrole/phthalocyanine hybrid films were investigated and compared to those of polypyrrole films. A gas sensor consisting in platinum microelectrodes arrays was fabricated using silicon microtechnologies, and the polypyrrole and polypyrrole/phthalocyanine films were electrochemically deposited on the platinum microelectrodes arrays of this gas sensor. When exposed to ammonia, polymer-based gas sensors exhibited a decrease in conductance due to the electron exchange between ammonia and sensitive polymer-based layer. The characteristics of the gas sensors (response time, response amplitude, reversibility) were studied for ammonia concentrations varying from 1 ppm to 100 ppm. Polypyrrole/phthalocyanine films exhibited a high sensitivity and low detection limit to ammonia as well as a fast and reproducible response at room temperature. The response to ammonia exposition of polypyrrole films was found to be strongly enhanced thanks to the incorporation of the phthalocyanine in the polypyrrole matrix. © 2013 Elsevier B.V. All rights reserved.

  15. Synthesis, photophysical and photochemical properties of zinc phthalocyanines bearing fluoro-functionalized substituents

    Energy Technology Data Exchange (ETDEWEB)

    Aktaş, Ayşe [Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey); Pişkin, Mehmet [Marmara University, Faculty of Art and Science, Department of Chemistry, 34722 Kadikoy-Istanbul (Turkey); Durmuş, Mahmut [Gebze Institute of Technology, Department of Chemistry, PO Box 141, Gebze 41400, Kocaeli (Turkey); Bıyıklıoğlu, Zekeriya, E-mail: zekeriya_61@yahoo.com [Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey)

    2014-01-15

    In this study, the synthesis of phthalonitrile derivatives bearing fluoro-functionalized groups and their peripherally-tetra substituted zinc phthalocyanine complexes were reported. The phthalonitrile derivatives 2a–5a were prepared by nucleophilic substitution of 4-nitrophthalonitrile with 2-[3-(trifluoromethyl)phenoxy]ethanol, 2-{2-[3-(trifluoromethyl) phenoxy]ethoxy}ethanol, 2-(2,3,5,6-tetrafluorophenoxy)ethanol, 2-[2-(2,3,5,6-tetrafluorophenoxy)ethoxy]ethanol, respectively. Zinc phthalocyanines bearing fluoro-functionalized groups (2b–5b) were obtained from the corresponding phthalonitrile derivatives. The newly synthesized phthalocyanines displayed good solubility in organic solvents such as chloroform (CHCl{sub 3}), dichloromethane (DCM), tetrahydrofuran (THF), toluene, dimethylformamide (DMF) and dimethylsulfoxide (DMSO). On the other hand, the singlet oxygen, photodegradation, fluorescence quantum yields and fluorescence lifetime of these complexes were determined in DMSO. The effects of the substitution with fluoro-functionalized groups on these parameters were also compared. -- Highlights: • Synthesis of peripherally substituted zinc phthalocyanines. • Photophysical and photochemical properties in DMSO for phthalocyanines. • Photodynamic therapy studies.

  16. Zinc phthalocyanine thin film and chemical analyte interaction studies by density functional theory and vibrational techniques.

    Science.gov (United States)

    Saini, G S S; Singh, Sukhwinder; Kaur, Sarvpreet; Kumar, Ranjan; Sathe, Vasant; Tripathi, S K

    2009-06-03

    Thin films of zinc phthalocyanine have been deposited on KBr and glass substrates by the thermal evaporation method and characterized by the x-ray diffraction, optical, infrared and Raman techniques. The observed x-ray diffraction and infrared absorption spectra of as-deposited thin films suggest the presence of an α crystalline phase. Infrared and Raman spectra of thin films after exposure to vapours of ammonia and methanol have also been recorded. Shifts in the position of some IR and Raman bands in the spectra of exposed films have been observed. Some bands also show changes in their intensity on exposure. Increased charge on the phthalocyanine ring and out-of-plane distortion of the core due to interaction between zinc phthalocyanine and vapour molecules involving the fifth coordination site of the central metal ion may be responsible for the band shifts. Changes in the intensity of bands are interpreted in terms of the lowering of molecular symmetry from D(4h) to C(4v) due to doming of the core. Molecular parameters and Mulliken atomic charges of zinc phthalocyanine and its complexes with methanol and ammonia have been calculated from density functional theory. The binding energy of the complexes have also been calculated. Calculated values of the energy for different complexes suggest that axially coordinated vapour molecules form the most stable complex. Calculated Mulliken atomic charges show net charge transfer from vapour molecules to the phthalocyanine ring for the most stable complex.

  17. Water soluble {2-[3-(diethylamino)phenoxy]ethoxy} substituted zinc(II) phthalocyanine photosensitizers

    Energy Technology Data Exchange (ETDEWEB)

    Çakır, Dilek [Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey); Göl, Cem [Gebze Institute of Technology, Department of Chemistry, PO Box 141, Gebze, 41400, Kocaeli (Turkey); Çakır, Volkan [Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey); Durmuş, Mahmut [Gebze Institute of Technology, Department of Chemistry, PO Box 141, Gebze, 41400, Kocaeli (Turkey); Bıyıklıoğlu, Zekeriya, E-mail: zekeriya_61@yahoo.com [Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey); Kantekin, Halit [Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey)

    2015-03-15

    The new peripherally and non-peripherally tetra-{2-[3-(diethylamino)phenoxy] ethoxy} substituted zinc phthalocyanines (2a and 3a) were synthesized by cyclotetramerization of phthalonitrile derivatives (2 and 3). 2-[3-(diethylamino)phenoxy] ethoxy group was chosen as substituent because the quaternization of the diethylamino functionality on the structure of this group produced water soluble zinc phthalocyanines (2b and 3b). The water solubility is very important for many different applications such as photosensitizers in the photodynamic therapy of cancer because the water soluble photosensitizers can be injected directly to the body and they can transport to cancer cells through blood stream. The new compounds were characterized by using elemental analysis, UV–vis, IR, {sup 1}H NMR, {sup 13}C NMR and mass spectroscopies. The photophysical and photochemical properties of these novel photosensitizer compounds were examined in DMSO (both non-ionic and ionic complexes) and in PBS (for ionic complexes) solutions. The investigation of these properties is very important for the usage of the compounds as photosensitizers for PDT because determination of these properties is the first stage of potential of the compounds as photosensitizers. The bovine serum albumin (BSA) and DNA binding behaviour of the studied water soluble zinc (II) phthalocyanines were also investigated in PBS solutions for the determination of biological activity of these compounds. - Highlights: • Synthesis of water soluble zinc phthalocyanines. • Photophysical and photochemical properties for phthalocyanines. • Photodynamic therapy studies.

  18. Zinc phthalocyanine labelled polyethylene glycol: preparation, characterization, interaction with bovine serum albumin and near infrared fluorescence imaging in vivo.

    Science.gov (United States)

    Lv, Feng; Cao, Bo; Cui, Yanli; Liu, Tianjun

    2012-05-25

    Zinc phthalocyanine labelled polyethylene glycol was prepared to track and monitor the in vivo fate of polyethylene glycol. The chemical structures were characterized by nuclear magnetic resonance and infrared spectroscopy. Their light stability and fluorescence quantum yield were evaluated by UV-Visible and fluorescence spectroscopy methods. The interaction of zinc phthalocyanine labelled polyethylene glycol with bovine serum albumin was evaluated by fluorescence titration and isothermal titration calorimetry methods. Optical imaging in vivo, organ aggregation as well as distribution of fluorescence experiments for tracking polyethylene glycol were performed with zinc phthalocyanine labelled polyethylene glycol as fluorescent agent. Results show that zinc phthalocyanine labelled polyethylene glycol has good optical stability and high emission ability in the near infrared region. Imaging results demonstrate that zinc phthalocyanine labelled polyethylene glycol can track and monitor the in vivo process by near infrared fluorescence imaging, which implies its potential in biomaterials evaluation in vivo by a real-time noninvasive method.

  19. Fluorescence behavior and singlet oxygen generating abilities of aluminum phthalocyanine in the presence of anisotropic gold nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Mthethwa, Thandekile; Nyokong, Tebello, E-mail: t.nyokong@ru.ac.za

    2015-01-15

    Gold nanoparticles (spheres, rods and bipyramids) were synthesized. The nanocrystals were characterized by UV–visible spectrometry, transmission electron microscopy (TEM) and X-ray diffractometry (XRD). The as prepared gold nanoparticles were then conjugated to a quaternized 2,(3)-tetra [2-(dimethylamino) ethanethio] substituted Al(OH) phthalocyanine (complex 1). The conjugation of phthalocyanines with gold nanoparticles resulted in a decrease in the fluorescence quantum yields and lifetimes. Conversely, an increase in the singlet oxygen quantum yields was observed for the conjugated complex 1 in the presence of AuNPs. - Highlights: • Gold nanoparticles (spheres, rods and bipyramids) were synthesized. • Gold nanoparticles were then conjugated to a quaternized ClAl phthalocyanine. • Conjugation of phthalocyanines with gold nanoparticles resulted in a decrease in the fluorescence quantum yields. • An increase in the singlet oxygen quantum yields was observed for the phthalocyanine in the presence of nanoparticles.

  20. Copper allergy from dental copper amalgam?

    Science.gov (United States)

    Gerhardsson, Lars; Björkner, Bert; Karlsteen, Magnus; Schütz, Andrejs

    2002-05-06

    A 65-year-old female was investigated due to a gradually increasing greenish colour change of her plastic dental splint, which she used to prevent teeth grinding when sleeping. Furthermore, she had noted a greenish/bluish colour change on the back of her black gloves, which she used to wipe her tears away while walking outdoors. The investigation revealed that the patient had a contact allergy to copper, which is very rare. She had, however, had no occupational exposure to copper. The contact allergy may be caused by long-term exposure of the oral mucosa to copper from copper-rich amalgam fillings, which were frequently used in childhood dentistry up to the 1960s in Sweden. The deposition of a copper-containing coating on the dental splint may be caused by a raised copper intake from drinking water, increasing the copper excretion in saliva, in combination with release of copper due to electrochemical corrosion of dental amalgam. The greenish colour change of the surface of the splint is probably caused by deposition of a mixture of copper compounds, e.g. copper carbonates. Analysis by the X-ray diffraction technique indicates that the dominant component is copper oxide (Cu2O and CuO). The corresponding greenish/bluish discoloration observed on the back of the patient's gloves may be caused by increased copper excretion in tears.

  1. Copper Products Capacity Expansion Stimulate the Copper Consumption

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    <正>The dramatic growth of copper consumption in China can directly be seen from the expansion of copper products capacity.According to sta- tistics,in the past 4 years,the improvement on the balance of trade on copper bar,copper,and copper alloy and copper wire & cable has driven the growth of copper consumption a lot.

  2. Tetra- and octa-[4-(2-hydroxyethyl)phenoxy bearing novel metal-free and zinc(II) phthalocyanines: Synthesis, characterization and investigation of photophysicochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Köksoy, Baybars [Marmara University, Department of Chemistry, 34722 Kadıköy, Istanbul (Turkey); Durmuş, Mahmut [Gebze Technical University, Department of Chemistry, 41400 Gebze, Kocaeli (Turkey); Bulut, Mustafa, E-mail: mbulut@marmara.edu.tr [Marmara University, Department of Chemistry, 34722 Kadıköy, Istanbul (Turkey)

    2015-05-15

    In this study, four novel phthalonitriles (1–4) and their corresponding metal-free (5–8) and zinc(II) phthalocyanine derivatives (9–12) bearing 4-(hydroxyethyl)phenoxy groups were synthesized. These novel compounds were characterized by IR, elemental analyses, {sup 1}H-NMR, UV–vis, and MALDI-TOF spectral data. Furthermore, photophysical (fluorescence quantum yields and lifetimes) and photochemical properties (singlet oxygen generation and photodegradation quantum yields) of these phthalocyanines were investigated in dimethylsulfoxide. The studied zinc(II) phthalocyanines generated highly singlet oxygen which is very important for the photodynamic therapy (PDT) of cancer. The fluorescence quenching behaviour of the newly synthesized phthalocyanine compounds were also investigated using 1,4-benzoquinone. - Highlights: • Octa and tetra 4-(hydroxyethyl)phenoxy substituted metal-free and zinc(II) phthalocyanines. • Study of photophysicochemical properties of eight new phthalocyanines. • Highly singlet oxygen generation for novel zinc(II) phthalocyanine photosensitizers.

  3. Au nanorods modulated NIR fluorescence and singlet oxygen generation of water soluble dendritic zinc phthalocyanine.

    Science.gov (United States)

    Zhou, Xuefei; He, Xiaohong; Wei, Shiliang; Jia, Kun; Liu, Xiaobo

    2016-11-15

    A novel cyano-terminated zinc phthalocyanine (ZnPc-CN) exhibiting visible near infrared (vis-NIR) emitting around 690nm in N,N-dimethylformamide (DMF) solvent has been synthesized. Furthermore, the peripheral cyano groups of newly synthesized zinc phthalocyanine were hydrolyzed in strong basic solution, leading to water soluble carboxylated zinc phthalocyanine (ZnPc-COOH) with completely quenched fluorescence in aqueous solution. Interestingly, we found that the NIR fluorescence of aqueous ZnPc-COOH was dramatically recovered in the presence of gold nanorods (Au NR), which was due to the alternation of ZnPc-COOH molecules self-assembling via electrostatic interaction between cetyltrimethylammonium bromide (CTAB) on the surface of Au NR and peripheral carboxyl of ZnPc-COOH. In addition, ZnPc-COOH/Au NR conjugates demonstrated an improved singlet oxygen generation, which could be served as potential bioimaging probe and photosensitizer for photodynamic therapy.

  4. A study of single-walled carbon nanotubes modified by organics of the phthalocyanine category

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Organics of the phthalocyanine category have very good nonlinear optical properties. The single-walled carbon nanotubes were modified by using the phenoxy phthalocyanine. Characterization analysis was made by means of the transmission electron microscope (TEM), ultraviolet visible absorptive spectra, fluorescent spectra and Raman spectra. Under the TEM, it was observed that the composite looked like sugarcoated haws. By comparing the ultraviolet visible absorptive spectra before and after absorption, it was disclosed that the spectral intensity and the intensity of the peaks in the fluorescent spectra dropped remarkably. This shows that the single-walled carbon nanotubes have absorbed a large number of phenoxy phthalocyanines. Raman analysis revealed that in the Raman spectra, the position of the main peaks of the single-walled carbon nanotubes after absorption moved in the direction of long waves. The analysis suggests that the movement of the Raman spectra results from the change in the state of the single-walled carbon nanotubes before and after absorption.

  5. Spectral, photophysical and photochemical properties of tetra- and octaglycosylated zinc phthalocyanines.

    Science.gov (United States)

    Iqbal, Zafar; Masilela, Nkosiphile; Nyokong, Tebello; Lyubimtsev, Alexey; Hanack, Michael; Ziegler, Thomas

    2012-04-01

    Photophysical and photochemical properties of a series of tetra- and octaglycosylated zinc phthalocyanines (ZnPcs) substituted with glucose and galactose moieties have been reported. Spectral properties of these phthalocyanines are compared in DMSO. Absorption spectra of the non-peripherally tetra-substituted ZnPcs 2 showed a significant red shift in their Q-band maxima as compared to the peripherally substituted analog 1. All the complexes gave high triplet quantum yields ranging from 0.68 to 0.88, whereas triplet lifetimes were in the range of 100-430 μs in argon-saturated solutions. The octagalactosylated ZnPc 3b showed the highest triplet quantum yield and singlet oxygen quantum yield of 0.88 and 0.69, respectively. The fluorescence quantum yields and lifetimes of all the compounds under investigation were within the range of zinc phthalocyanine complexes.

  6. Modern synthetic tools toward the preparation of sophisticated phthalocyanine-based photoactive systems.

    Science.gov (United States)

    Ragoussi, Maria-Eleni; Torres, Tomás

    2014-10-01

    Phthalocyanines are ideal components in a variety of electronic applications due to their extraordinary photophysical characteristics combined with their synthetic versatility and robustness. They have attracted substantial attention in recent decades and are now established building blocks of sophisticated molecular materials. Synthetically, a great deal of this progress is attributed to the use of modern synthetic tools, which gave rise to phthalocyanine-based systems that could not have been envisaged in the past. In particular, Pd-catalyzed cross-coupling reactions, together with other transition-metal-catalyzed procedures, "click" chemistry, and ruthenium metathesis have been employed extensively en route to an abundant range of elaborate phthalocyanine mono- and multicomponent photoactive architectures. Herein, we describe the synthesis of a selection of key examples that are representative in certain optoelectronic applications. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Charge transfer from and to manganese phthalocyanine: bulk materials and interfaces.

    Science.gov (United States)

    Rückerl, Florian; Waas, Daniel; Büchner, Bernd; Knupfer, Martin; Zahn, Dietrich R T; Haidu, Francisc; Hahn, Torsten; Kortus, Jens

    2017-01-01

    Manganese phthalocyanine (MnPc) is a member of the family of transition-metal phthalocyanines, which combines interesting electronic behavior in the fields of organic and molecular electronics with local magnetic moments. MnPc is characterized by hybrid states between the Mn 3d orbitals and the π orbitals of the ligand very close to the Fermi level. This causes particular physical properties, different from those of the other phthalocyanines, such as a rather small ionization potential, a small band gap and a large electron affinity. These can be exploited to prepare particular compounds and interfaces with appropriate partners, which are characterized by a charge transfer from or to MnPc. We summarize recent spectroscopic and theoretical results that have been achieved in this regard.

  8. Zinc phthalocyanine-conjugated with bovine serum albumin mediated photodynamic therapy of human larynx carcinoma

    Science.gov (United States)

    Silva, E. P. O.; Santos, E. D.; Gonçalves, C. S.; Cardoso, M. A. G.; Soares, C. P.; Beltrame, M., Jr.

    2016-10-01

    Phthalocyanines, which are classified as second-generation photosensitizers, have advantageous photophysical properties, and extensive studies have demonstrated their potential applications in photodynamic therapy. The present work describes the preparation of a new zinc phthalocyanine conjugated to bovine serum albumin (compound 4a) and its photodynamic efficiency in human larynx-carcinoma cells (HEp-2 cells). The unconjugated precursor (compound 4) was also studied. Compounds 4 and 4a penetrated efficiently into the cell, exhibiting cytoplasmic localization, and showed no cytotoxicity in the dark. However, high photodynamic activities were observed in HEp-2 cells after treatments with 5 µM photosensitizers and 4.5 J cm-2 light. These conditions were sufficient to decrease the cell viability to 57.93% and 32.75% for compounds 4 and 4a, respectively. The present results demonstrated high photodynamic efficiency of zinc phthalocyanine conjugated with bovine serum albumin in destroying the larynx-carcinoma cells.

  9. Effect of axial ligands on the molecular configurations, stability, reactivity, and photodynamic activities of silicon phthalocyanines.

    Science.gov (United States)

    Luan, Liqiang; Ding, Lanlan; Shi, Jiawei; Fang, Wenjuan; Ni, Yuxing; Liu, Wei

    2014-12-01

    To demonstrate the effect of axial ligands on the structure-activity relationship, a series of axially substituted silicon phthalocyanines (SiPcs) have been synthesized with changes to the axial ligands. The reactivity of the axial ligand upon shielding by the phthalocyanine ring current, along with their stability, photophysical, and photodynamic therapy (PDT) activities were compared and evaluated for the first time. As revealed by single-crystal XRD analysis, rotation of the axial -OMe ligands was observed in SiPc 3, which resulted in two molecular configurations coexisting synchronously in both the solid and solution states and causing a split of the phthalocyanine α protons in the (1)H NMR spectra that is significantly different from all SiPcs reported so far. The remarkable photostability, good singlet oxygen quantum yield, and efficient in vitro photodynamic activity synergistically show that compound 3 is one of the most promising photosensitizers for PDT.

  10. Nonlinear optical and optical limiting properties of polymeric carboxyl phthalocyanine coordinated with rare earth atom

    Science.gov (United States)

    Zhao, Peng; Wang, Zonghua; Chen, Jishi; Zhou, Yu; Zhang, Fushi

    2017-04-01

    The nonlinear optical properties of the polymeric carboxyl phthalocyanine with lanthanum (LaPPc.COOH), holmium (HoPPc.COOH) and ytterbium (YbPPc.COOH) as centric atom, were investigated by the Z-scan method using a picosecond 532 nm laser. The synthesized phthalocyanines had steric polymeric structure and dissolved well in aqueous solution. The nonlinear optical response of them was attributed to the reverse saturable absorption and self-focus refraction. The nonlinear absorption properties decreased with the centric atoms changing from La, Ho to Yb. The largest second-order hyperpolarizability and optical limiting response threshold of LaPPc.COOH were 3.89 × 10-29 esu and 0.32 J/cm2, respectively. The reverse saturable absorption was explained by a three level mode of singlet excited state under the picosecond irradiation. The result indicates the steric structure presented additive stability of these polymeric phthalocyanines for their application as potential optical limiting materials.

  11. Azide-derivatized gold nanosphere "clicked" to indium and zinc phthalocyanines for improved nonlinear optical limiting

    Science.gov (United States)

    Bankole, Owolabi M.; Nyokong, Tebello

    2017-05-01

    We report on the conjugation of azide-derivatized gold nanoparticles (AuNPs) to alkyne moieties of ZnPc and InPc via azide-alkyne Huisgen cycloaddition reaction to form phthalocyanines-AuNPs (MPc-AuNPs) conjugates. The detailed structural characterizations of the composites were in good agreement with the expected results. The nonlinear absorption coefficients and other nonlinear optical limiting parameters were almost two times larger for the conjugates compared to free phthalocyanines. We established direct relationship between improved photophysical characterizations and enhanced nonlinear effects of reverse saturable absorption mechanisms favoured by excited triplet absorption of the phthalocyanines in the presence of AuNPs. The combination of InPc with AuNPs resulted in the lowest limiting intensity value of 0.06 J/cm2, hence the best performance in terms of optical limiting.

  12. Antwerp Copper Plates

    DEFF Research Database (Denmark)

    Wadum, Jørgen

    1999-01-01

    In addition to presenting a short history of copper paintings, topics detail artists’ materials and techniques, as well as aspects of the copper industry, including mining, preparation and trade routes.......In addition to presenting a short history of copper paintings, topics detail artists’ materials and techniques, as well as aspects of the copper industry, including mining, preparation and trade routes....

  13. Copper and copper proteins in Parkinson's disease.

    Science.gov (United States)

    Montes, Sergio; Rivera-Mancia, Susana; Diaz-Ruiz, Araceli; Tristan-Lopez, Luis; Rios, Camilo

    2014-01-01

    Copper is a transition metal that has been linked to pathological and beneficial effects in neurodegenerative diseases. In Parkinson's disease, free copper is related to increased oxidative stress, alpha-synuclein oligomerization, and Lewy body formation. Decreased copper along with increased iron has been found in substantia nigra and caudate nucleus of Parkinson's disease patients. Copper influences iron content in the brain through ferroxidase ceruloplasmin activity; therefore decreased protein-bound copper in brain may enhance iron accumulation and the associated oxidative stress. The function of other copper-binding proteins such as Cu/Zn-SOD and metallothioneins is also beneficial to prevent neurodegeneration. Copper may regulate neurotransmission since it is released after neuronal stimulus and the metal is able to modulate the function of NMDA and GABA A receptors. Some of the proteins involved in copper transport are the transporters CTR1, ATP7A, and ATP7B and the chaperone ATOX1. There is limited information about the role of those biomolecules in the pathophysiology of Parkinson's disease; for instance, it is known that CTR1 is decreased in substantia nigra pars compacta in Parkinson's disease and that a mutation in ATP7B could be associated with Parkinson's disease. Regarding copper-related therapies, copper supplementation can represent a plausible alternative, while copper chelation may even aggravate the pathology.

  14. Improved photodynamic efficacy of Zn(II) phthalocyanines via glycerol substitution.

    Science.gov (United States)

    Chin, Yunni; Lim, Siang Hui; Zorlu, Yunus; Ahsen, Vefa; Kiew, Lik Voon; Chung, Lip Yong; Dumoulin, Fabienne; Lee, Hong Boon

    2014-01-01

    Phthalocyanines are excellent photosensitizers for photodynamic therapy as they have strong absorbance in the near infra-red region which is most relevant for in vivo activation in deeper tissular regions. However, most phthalocyanines present two major challenges, ie, a strong tendency to aggregate and low water-solubility, limiting their effective usage clinically. In the present study, we evaluated the potential enhancement capability of glycerol substitution on the photodynamic properties of zinc (II) phthalocyanines (ZnPc). Three glycerol substituted ZnPc, 1-3, (tetra peripherally, tetra non-peripherally and mono iodinated tri non-peripherally respectively) were evaluated in terms of their spectroscopic properties, rate of singlet oxygen generation, partition coefficient (log P), intracellular uptake, photo-induced cytotoxicity and vascular occlusion efficiency. Tetrasulfonated ZnPc (ZnPcS4) was included as a reference compound. Here, we showed that 1-3 exhibited 10-100 nm red-shifted absorption peaks with higher molar absorptivity, and at least two-fold greater singlet oxygen generation rates compared to ZnPcS4. Meanwhile, phthalocyanines 1 and 2 showed more hydrophilic log P values than 3 consistent with the number of glycerol attachments but 3 was most readily taken up by cells compared to the rest. Both phthalocyanines 2 and 3 exhibited potent phototoxicity against MCF-7, HCT-116 and HSC-2 cancer cell-lines with IC50 ranging 2.8-3.2 µM and 0.04-0.06 µM respectively, while 1 and ZnPcS4 (up to 100 µM) failed to yield determinable IC50 values. In terms of vascular occlusion efficiency, phthalocyanine 3 showed better effects than 2 by causing total occlusion of vessels with diameter glycerol substitution, in particular in structures 2 and 3, is able to improve the photodynamic properties of ZnPc.

  15. High rectification in organic diodes based on liquid crystalline phthalocyanines.

    Science.gov (United States)

    Apostol, Petru; Eccher, Juliana; Dotto, Marta Elisa Rosso; Costa, Cassiano Batesttin; Cazati, Thiago; Hillard, Elizabeth A; Bock, Harald; Bechtold, Ivan H

    2015-12-28

    The optical and electrical properties of mesogenic metal-free and metalated phthalocyanines (PCs) with a moderately sized and regioregular alkyl periphery were investigated. In solution, the individualized molecules show fluorescence lifetimes of 4-6 ns in THF. When deposited as solid thin films the materials exhibit significantly shorter fluorescence lifetimes with bi-exponential decay (1.4-1.8 ns; 0.2-0.4 ns) that testify to the formation of aggregates viaπ-π intermolecular interactions. In diode structures, their pronounced columnar order outbalances the unfavorable planar alignment and leads to excellent rectification behavior. Field-dependent charge carrier mobilities are obtained from the J-V curves in the trap-limited space-charge-limited current regime and demonstrate that the metalated PCs display an improved electrical response with respect to the metal-free homologue. The excited-state lifetime characterization suggest that the π-π intermolecular interactions are stronger for the metal-free PC, confirming that the metallic centre plays an important role in the charge transport inside these materials.

  16. Surface Morphology of Annealed Lead Phthalocyanine Thin Films

    Directory of Open Access Journals (Sweden)

    P.Kalugasalam,

    2010-06-01

    Full Text Available The thin films of Lead Phthalocyanine (PbPc on glass substrates were prepared by Vacuum deposition. The thickness of the films was 450 nm. The sample annealed in high vacuum at 373 K temperature. The sample has been analysed by X-ray diffraction, scanning electron microscopy and atomic force microscopy in order to get structural and surface morphology of the PbPc thin film. The formation of XRD patterns of PbPc shows a triclinic grains (T seen along with monoclinic (M forms of PbPc. The sample is annealed at 373 K temperatures; the film shows peaks that assigned to the triclinic phase. SEM and AFM are the best tools to investigate the surface smoothness and to find the grain size of the particles. The grain size is calculated for all films of different thicknesses. The annealed AFM micrograph shows that the surface of the films consists of large holes. The annealed AFM image indicates a smooth surface. It is very clear that the grain size decreases with increase in the annealing temperature. The roughness also decreases with the increase in film annealing temperature. Annealed film leads to the oxidation of the hthalocyanine with oxygen absorbed or diffused. Therefore, the heat is responsible for the increase in film thickness. Since the films expand, it is believed that the porosity is increased.

  17. Synthesis of phthalocyanine derivatives as materials for organic photovoltaic cells

    Science.gov (United States)

    Collazo-Ramos, Aura

    Organic photovoltaics (OPVs) are used to convert sunlight into electricity by using thin films of organic semiconductors. OPVs have the potential to produce low cost, lightweight, flexible devices with an eased manufacturing process. This technology contains the potential to increase the use of clean, sustainable solar energy, helping manage the global energy and environmental crisis that results majorly from the constant use of fossil fuels as an energy source. The ability to modulate the physical properties of organic molecules by tuning their chemical structure is an advantage for OPVs. Phthalocyanines (Pcs) are highly pi-conjugated synthetic porphyrin analogs that have been explored as active layer components in OPVs due to their high extinction coefficients and hole mobilities. The Pc structure can be modified by the introduction of metals in the core and the incorporation of substituents into the periphery. These modifications tend to tune the solubility, photophysical properties and condensed phase organization of Pcs. The research work in this dissertation describes improved methods towards substituted Pc derivatives addressing: (1) the use of mass spectrometry techniques for Pcs characterization, (2) efforts to achieve materials with near-infrared (NIR) absorption, and (3) the potential of Pc as electron-acceptor materials. Herein, the synthesis of a series of asymmetric and symmetric metallated Pcs has been established, which resulted in interesting chemical, photophysical and electrochemical properties. The materials investigated in this thesis increase the potential of Pcs as organic semiconductors for OPVs.

  18. Mixed configuration ground state in iron(II) phthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez-Rodriguez, Javier; Toby, Brian; van Veenendaal, Michel

    2015-06-23

    We calculate the angular dependence of the x-ray linear and circular dichroism at the L2,3 edges of α-Fe(II) Phthalocyanine (FePc) thin films using a ligand-field model with full configuration interaction. We find the best agreement with the experimental spectra for a mixed ground state of 3E (a2 e3b1 ) and 3B (a1 e4b1 ) g 1g g 2g 2g 1g g 2g with the two configurations coupled by the spin-orbit interaction. The 3Eg(b) and 3B2g states have easy-axis and easy-plane anisotropies, respectively. Our model accounts for an easy-plane magnetic anisotropy and the measured magnitudes of the in-plane orbital and spin moments. The proximity in energy of the two configurations allows a switching of the magnetic anisotropy from easy plane to easy axis with a small change in the crystal field, as recently observed for FePc adsorbed on an oxidized Cu surface. We also discuss the possibility of a quintet ground state (5A1g is 250 meV above the ground state) with planar anisotropy by manipulation of the Fe-C bond length by depositing the complex on a substrate that is subjected to a mechanical strain.

  19. Organic semiconductor nickel phthalocyanine-based photocapacitive and photoresistive detector

    Science.gov (United States)

    Shah, Mutabar; Karimov, Kh S.; Sayyad, M. H.

    2010-07-01

    In this study, the photosensitive organic semiconductor nickel phthalocyanine (NiPc) is investigated as a photocapacitive and photoresistive detector. NiPc thin film is grown by vacuum thermal evaporation on an indium tin oxide (ITO)-coated glass substrate. Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is deposited as a top electrode by drop-casting to fabricate the ITO/NiPc/PEDOT:PSS light detector. It has been observed that under the unmodulated filament lamp illumination of up to 9720 lux the capacitance of the detectors increased up to 21, 18 and 4% at a frequency of measuring voltage of 120 Hz, 1 kHz and 10 kHz, respectively, under dark conditions. The change in resistance with the variation in the intensity of light is also investigated. The capacitance and resistance of the light detector decrease with an increase in the frequency. It is assumed that the photocapacitive and photoresistive response of the detector is associated with polarization occurring due to the transfer of photo-generated electrons and holes. The calculated results are in reasonable agreement with the experimental results.

  20. A novel family of diarylethene-phthalocyanine dyad systems for nondestructive data processing

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A novel family of diarylethene (DTE)-phthalocyanine (Pc) dyad systems were designed and synthesized. It was found that the significant change in the extension of the linear π-conjugation of DTE when irradiated by 254 nm UV light directly made the absorption of the Q-band of phthalocyanine decrease. Detecting the absorption changes of the Q-band would not induce the reversible photochromic reaction. Therefore, non-destructive readout was feasible based on the spectral changes of the Q-band when such materials were used as storage media.

  1. Application of nanophotosensitizers (aluminum phthalocyanine nanoparticles) for early diagnosis and prevention of inflammatory diseases

    Science.gov (United States)

    Kuznetsova, J. O.; Makarov, V. I.

    2016-08-01

    This paper deals with a possibility of new types of photosensitizers application - Aluminum Phthalocyanine nanoparticles (nAlPc) in clinical practice for diagnosis, prevention and therapy of inflammatory diseases in dentistry and traumatology. It was detected that the aluminum phthalocyanine (AlPc) fluoresces in the nanoparticle form in the presence of pathologic microflora or inflammation process. It will make possible to detect the local accumulation of pathological microflora on the enamel surface and also for diagnostics and treatment of inflammatory diseases. Experimental studies of interaction of NP-AlPc with tooth enamel and with biological joint tissue at arthrosis are presented.

  2. Unsymmetrical extended -conjugated zinc phthalocyanine for sensitization of nanocrystalline TiO2 films

    Indian Academy of Sciences (India)

    L Giribabu; Ch Vijay Kumar; P Yella Reddy; Jun-Ho Yum; M Grätzel; Md K Nazeeruddin

    2009-01-01

    We have designed and synthesized a new unsymmetrical zinc phthalocyanine based on `push-pull’ and extended -conjugation concept, PCH008. The new sensitizer was fully characterized by CHN anlysis, UV-Vis., fluorescence spectroscopies and cyclic voltammetry. The new sensitizer which upon anchoring onto nanocrystalline TiO2 film exhibit a short circuit current of 5.63 mA cm-2, open circuit potential of 557.0 mV and a fill factor of 0.75 corresponding to an overall conversion efficiency of 2.35% under standard global air mass (AM) 1.5 solar conditions and compared its performance with literature reported phthalocyanine dyes.

  3. Picosecond optical nonlinearities in symmetrical and unsymmetrical phthalocyanines studied using the Z-scan technique

    Indian Academy of Sciences (India)

    S Venugopal Rao; P T Anusha; L Giribabu; Surya P Tewari

    2010-11-01

    We present our experimental results on the picosecond nonlinear optical (NLO) studies of symmetrical and unsymmetrical phthalocyanines, examined using the Z-scan technique. Both the open-aperture and closed-aperture Z-scan curves for three samples were recorded and the nonlinear coefficients were extracted from the theoretical fits. The nonlinear absorption/refraction contribution from the solvent was also identified. The observed open aperture behaviour for these molecules is understood in terms of the absorption coefficients of these molecules near 800 nm and the peak intensities used. It is established that these phthalocyanines exhibit large optical nonlinearities and, hence, are suitable for optical limiting applications.

  4. A novel family of diarylethene-phthalocyanine dyad systems for nondestructive data processing

    Institute of Scientific and Technical Information of China (English)

    CHEN ZiHui; LI ZhongYu; BIN YueJing; HUANG Lei; ZHANG FuShi

    2008-01-01

    A novel family of diarylethene (DTE)-phthalocyanine (Pc) dyad systems were designed and synthesized. It was found that the significant change in the extension of the linear n-conjugation of DTE when irra-diated by 254 nm UV light directly made the absorption of the Q-band of phthalocyanine decrease. De-tecting the absorption changes of the Q-band would not induce the reversible photochromic reaction. Therefore, non-destructive readout was feasible based on the spectral changes of the Q-band whensuch materials were used as storage media.

  5. Electronic Structures of Asymmetrically Substituted Phthalocyanines and Their Second Non-linear Optical Properties

    Institute of Scientific and Technical Information of China (English)

    张天莉; 严继民

    2001-01-01

    Quantum-chemical AM1 calculations were performed to study the geometries,the electronic structures and the second nonlinear optical properties of phthalocyanine and some asymmetrically substituted phthalocyanines,which include tert-butyl,amino,dimethylamino,nitro,fluoro,chloro,bromo iodo and nitrile substituents. The relationships of the second nonlinear optical coefficients β with dipole moment μ, and β with the energy-gap differences of frontier orbitals ΔEDA were discussed. Two relationships are regular and all ΔEDA-μ show very good linear relationship.

  6. [Optical limiting cycling performance and photostability of vanadyl phthalocyanines and naphthalocyanines].

    Science.gov (United States)

    Feng, Miao; Zhen, Xiao; Zheng, Chan; Huang, Juan; Zhan, Hong-Bing

    2008-01-01

    Optical limiting (OL) cycling performance and photostability of vanadyl phthalocyanines (VOPcs) and naphthalocyanines (VONcs) were studied. The results show that although vanadyl 2,11,20,29-tetra-tert-butyl-2,3-naphthalocyanine has the most pronounced OL effect originally, it is not a promising OL material due to its poor photostability. Meanwhile, vanadyl 2,9, 16,23-etraphenoxy-29H, 31H-phthalocyanine is considered to be a potential OL material, owing to its considerable OL effect and good photostability. A possible photochemical mechanism behind the reverse saturable absorption (RSA) and photolysis process of the studied species is proposed.

  7. Photocatalytic degradation of polystyrene plastic under fluorescent light.

    Science.gov (United States)

    Shang, Jing; Chai, Ming; Zhu, Yongfa

    2003-10-01

    Plastic is used widely all over the world, due to the fact that it is low cost, is easily processable, and has lightweight properties. However, the hazard of discarding waste plastic, so-called "white pollution", is becoming more and more severe. In this paper, solid-phase photocatalytic degradation of polystyrene (PS) plastic, one of the most common commercial plastics, over copper phthalocyanine (CuPc) sensitized TiO2 photocatalyst (TiO2/CuPc) has been investigated under fluorescent light irradiation in the air. UV-vis spectra show that TiO2/CuPc extends its photoresponse range to visible light, contrasting to only UV light absorption of pure TiO2. The PS photodegradation experiments exhibit that higher PS weight loss rate, lower PS average molecular weight, less amount of volatile organic compounds, and more CO2 can be obtained in the system of PS-(TiO2/CuPc), in comparison with the PS-TiO2 system. Therefore, PS photodegradation over TiO2 CuPc composite is more complete and efficient than over pure TiO2, suggesting the potential application of dye-sensitized TiO2 catalyst in the thorough photodegradation of PS plastic under fluorescent light. During the photodegradation of PS plastic, the reactive oxygen species generated on TiO2 or TiO2/CuPc particle surfaces play important roles in chain scission. The present study demonstrates that the combination of polymer plastic with dye-sensitized TiO2 catalyst in the form of thin film is a practical and useful way to photodegrade plastic contaminants in the sunlight.

  8. Electrical characterization of the organic semiconductor Ag/CuPc/Au Schottky diode

    Institute of Scientific and Technical Information of China (English)

    Mutabar Shah; M. H. Sayyad; Kh. S. Karimov

    2011-01-01

    This paper reports on the fabrication and investigation of a surface-type organic semiconductor copper phthalocyanine (CuPc) based diode. A thin film of CuPc of thickness 100 nm was thermally sublimed onto a glass substrate with preliminary deposited metallic electrodes to form a surface-type Ag/CuPc/Au Schottky diode. The current-voltage characteristics were measured at room temperature under dark conditions. The barrier height was calculated as 1.05 eV. The values of mobility and conductivity was found to be 1.74 x l0-9 cm2/(V.s) and 5.5 x 10-6 Ω-1. cm-1, respectively. At low voltages the device showed ohmic conduction and the space charge limited current conduction mechanisms were dominated at higher voltages.

  9. Critical CuI buffer layer surface density for organic molecular crystal orientation change

    Science.gov (United States)

    Ahn, Kwangseok; Kim, Jong Beom; Kim, Hyo Jung; Lee, Hyun Hwi; Lee, Dong Ryeol

    2015-01-01

    We have determined the critical surface density of the CuI buffer layer inserted to change the preferred orientation of copper phthalocyanine (CuPc) crystals grown on the buffer layer. X-ray reflectivity measurements were performed to obtain the density profiles of the buffer layers and out-of-plane and 2D grazing-incidence X-ray diffraction measurements were performed to determine the preferred orientations of the molecular crystals. Remarkably, it was found that the preferred orientation of the CuPc film is completely changed from edge-on (1 0 0) to face-on (1 1 -2) by a CuI buffer layer with a very low surface density, so low that a large proportion of the substrate surface is bare.

  10. Significant Improvement of Organic Thin-Film Transistor Mobility Utilizing an Organic Heterojunction Buffer Layer

    Institute of Scientific and Technical Information of China (English)

    PAN Feng; QIAN Xian-Rui; HUANG Li-Zhen; WANG Hai-Bo; YAN Dong-Hang

    2011-01-01

    High-mobility vanadyl phthalocyanine (VOPc)/5,5″′-bis(4-fluorophenyl)-2,2′:5′,2″:5″,2″′-quaterthiophene (F2-P4T) thin-film transistors are demonstrated by employing a copper hexadecafluorophthalocyanine (F16 CuPc)/copper phthalocyanine (CuPc) heterojunction unit,which are fabricated at different substrate temperatures,as a buffer layer. The highest mobility of 4.08cm2/Vs is achieved using a F16CuPc/CuPc organic heterojunction buffer layer fabricated at high substrate temperature.Compared with the random small grain-like morphology of the room-temperature buffer layer,the high-temperature organic heterojunction presents a large-sized fiber-like film morphology,resulting in an enhanced conductivity.Thus the contact resistance of the transistor is significantly reduced and an obvious improvement in device mobility is obtained.

  11. Analytical approaches for clarification of DNA-double decker phthalocyanine binding mechanism: As an alternative anticancer chemotherapeutic

    Science.gov (United States)

    Bağda, Esra; Yabaş, Ebru; Bağda, Efkan

    2017-02-01

    In the present study a novel water soluble double-decker phthalocyanine was synthesized and calf thymus DNA interaction of the synthesized double-decker phthalocyanine was investigated. 5-(3-pyridyl)-1,3,4-oxadiazole substituted phthalonitrile 1 was prepared by a nucleophilic displacement reaction of 4-nitrophthalonitrile with 5-(3-pyridyl)-1,3,4-oxadiazole-2-thiol. Lutetium(III) double-decker phthalocyanine 2 was prepared by cyclotetramerization of compound 1. Water soluble lutetium(III) double-decker phthalocyanine 3 was prepared with quaternarization of compound 2. The synthesized double-decker phthalocyanine and calf thymus DNA interaction was investigated with UV-vis titrimetric methods, gel electrophoresis, and viscosity measurements. The fluorometric ethidium bromide replacement assay was conducted to clarify the binding mode of water soluble double-decker phthalocyanine. The thermodynamic parameters for interaction, K, ΔG0, ΔH0 and ΔS0 were calculated between the temperature ranges of 25 °C-75 °C. To the best of our knowledge, this is the first study about a double-decker phthalocyanine and DNA interaction.

  12. Effects of central metal on electronic structure, magnetic properties, infrared and Raman spectra of double-decker phthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Suzuki, Atsushi, E-mail: suzuki@mat.usp.ac.jp; Oku, Takeo

    2016-09-01

    Graphical abstract: - Highlights: • Electron density distributions were delocalized on the phthalocyanine rings. • The chemical shift was separated by the nuclear quadrupole interaction based on the EFG and η. • The magnetic parameters were dependent on the perturbation of the crystal field. • The vibration modes were shifted by the asymmetrical structure. - Abstract: The effects of the central metal in double-decker metal phthalocyanine on the electronic structure, magnetic properties, and infrared and Raman spectra of the complex were investigated. Electron density distributions were delocalized on the phthalocyanine rings. The narrow energy gap and infrared peaks observed in the ultra-violet–visible–near infrared spectra of the systems were attributed to phthalocyanine ring–ring interactions the between overlapping π-orbitals on each ring. The chemical shift behavior of the phthalocyanine rings was separated by the deformation of their structure owing to nuclear magnetic interaction of the nuclear quadrupole interaction as determined by the electronic field gradient and asymmetric parameters. The magnetic parameters of principle g-tensors were dependent on the perturbation of the crystal field by the hybridization of the d-spin in the central metal conjugated with nitrogen ligands. In the case of the vanadyl system, the IR vibration modes were shifted by the soft vibration mode for resolving the symmetrical structure. Inactive Raman vibration modes arose from no-polarization on the phthalocyanine rings. Double-decker metal phthalocyanines have great advantages for the control of the magnetic mechanism for quantum spin entanglement in the relaxation process.

  13. Pyrite nanoparticles as a Fenton-like reagent for in situ remediation of organic pollutants

    Directory of Open Access Journals (Sweden)

    Carolina Gil-Lozano

    2014-06-01

    Full Text Available The Fenton reaction is the most widely used advanced oxidation process (AOP for wastewater treatment. This study reports on the use of pyrite nanoparticles and microparticles as Fenton reagents for the oxidative degradation of copper phthalocyanine (CuPc as a representative contaminant. Upon oxidative dissolution in water, pyrite (FeS2 particles can generate H2O2 at their surface while simultaneously promoting recycling of Fe3+ into Fe2+ and vice versa. Pyrite nanoparticles were synthesized by the hot injection method. The use of a high concentration of precursors gave individual nanoparticles (diameter: 20 nm with broader crystallinity at the outer interfaces, providing a greater number of surface defects, which is advantageous for generating H2O2. Batch reactions were run to monitor the kinetics of CuPc degradation in real time and the amount of H2O2. A markedly greater degradation of CuPc was achieved with nanoparticles as compared to microparticles: at low loadings (0.08 mg/L and 20 h reaction time, the former enabled 60% CuPc removal, whereas the latter enabled only 7% removal. These results confirm that the use of low concentrations of synthetic nanoparticles can be a cost effective alternative to conventional Fenton procedures for use in wastewater treatment, avoiding the potential risks caused by the release of heavy metals upon dissolution of natural pyrites.

  14. Consistency in Al/CuPc/ n-Si Heterojunction Diode Parameters Extracted Using Different Techniques

    Science.gov (United States)

    Ullah, Irfan; Shah, Mutabar; Khan, Majid; Wahab, Fazal

    2016-02-01

    This paper reports fabrication and characterization of an Al/CuPc/ n-Si heterojunction diode. The heterojunction was fabricated by depositing the active organic semiconducting material copper phthalocyanine (CuPc) on the n-Si substrate using the thermal vacuum evaporation technique. Electrical characterization of the fabricated heterojunction was carried out at ambient conditions. Various diode parameters, such as the ideality factor ( n), barrier height (Φ_{{b}}), and series resistance ( R s), were extracted from the current-voltage ( I- V) characteristic curve. These parameters are consistent with techniques used by Cheung, Norde and Hernandez et al. Furthermore these parameters are consistent with capacitance-voltage (C-V) characterization method. The conduction mechanism at the interface of CuPc and n-Si was also investigated. The surface morphology of the CuPc film was studied using atomic force microscopy and scanning electron microscopy. The optical bandgap of the CuPc film was calculated from the absorption spectrum using Tauc's law.

  15. A study on threshold voltage stability of low operating voltage organic thin-film transistors

    Science.gov (United States)

    Padma, N.; Sen, Shaswati; Sawant, Shilpa N.; Tokas, R.

    2013-08-01

    A low operating voltage (<2 V) organic field-effect transistor (OFET) using phenylhexyltrichlorosilane (PTS) self-assembled monolayer (SAM) dielectric and copper phthalocyanine (CuPc) as semiconductor with improved mobility (0.035 cm2 V-1 s-1) and threshold voltage stability was demonstrated. This device showed better performance when compared to an OFET with octyltrichlorosilane (OTS-8) SAM dielectric. The improved mobility was attributed to the 2D growth mode of CuPc on PTS SAM because of surface energy matching between the two, whereas CuPc film on OTS-8 showed a 3D growth mode with larger grain boundary density. The higher threshold voltage stability of OFETs on PTS SAM was attributed to the efficient coverage and screening of trap centres at dielectric/semiconductor interface due to stronger intermolecular linking and formation of closely packed surface by the bulky phenyl end groups. Decrease in grain boundaries offered by 2D growth of CuPc for electron and hole trapping was also found to be another reason for improved threshold voltage stability. The results indicated that the nature of the end group of SAM dielectric, surface chemistry of dielectric and initial growth mode of semiconductors are all responsible for improvement in threshold voltage stability and enhanced performance of OFET.

  16. Fabrication and Electromagnetic Properties of Conjugated NH2-CuPc@Fe3O4

    Science.gov (United States)

    Yan, Liang; Pu, Zejun; Xu, Mingzhen; Wei, Renbo; Liu, Xiaobo

    2017-10-01

    Conjugated amino-phthalocyanine copper containing carboxyl groups/magnetite (NH2-CuPc@Fe3O4) has been fabricated from FeCl3·6H2O and NH2-CuPc via a simple solvothermal method and its electromagnetic properties investigated. Scanning electron microscopy and transmission electron microscopy revealed that the NH2-CuPc@Fe3O4 was a waxberry-like nanomaterial with NH2-CuPc molecules effectively embedded in the interior of Fe3O4 particles in the form of beads. Introduction of NH2-CuPc effectively improved the complementarity between the dielectric and magnetic losses of the system, resulting in excellent electromagnetic performance. The minimum reflection loss of the as-prepared composite reached -33.4 dB at 7.0 GHz for coating layer thickness of 4.0 mm and bandwidth below -10.0 dB (90% absorption) of up to 3.8 GHz. These results indicate that introduction of NH2-CuPc results in a composite with potential for use as an electromagnetic microwave absorption material.

  17. Structural and electronic implications for carrier injection into organic semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Castellani, Mauro [Universitaet Potsdam, Institut fuer Physik und Astronomie, Potsdam-Golm (Germany); Salzmann, Ingo; Yu, Shuwen; Koch, Norbert [Humboldt-Universitaet zu Berlin, Institut fuer Physik, Berlin (Germany); Bugnon, Philippe [Ecole Polytechnique Federale de Lausanne (Switzerland). Institut des Materiaux; Oehzelt, Martin [Johannes Kepler Universitaet Linz (Austria). Institut fuer Experimentalphysik

    2009-10-15

    We report on the structural and electronic interface formation between ITO (indium-tin-oxide) and prototypical organic small molecular semiconductors, i.e., CuPc (copper phthalocyanine) and {alpha}-NPD (N,N'-di(naphtalen-1-yl)-N,N'-diphenyl-benzidine). In particular, the effects of in situ oxygen plasma pretreatment of the ITO surface on interface properties are examined in detail: Organic layer-thickness dependent Kelvin probe measurements revealed a good alignment of the ITO work function and the highest occupied electronic level of the organic material in all samples. In contrast, the electrical properties of hole-only and bipolar organic diodes depend strongly on the treatment of ITO prior to organic deposition. This dependence is more pronounced for diodes made of polycrystalline CuPc than for those of amorphous {alpha}-NPD layers. X-ray diffraction and atomic force microscopic (AFM) investigations of CuPc nucleation and growth evidenced a more pronounced texture of the polycrystalline film structure on the ITO substrate that was oxygen plasma treated prior to organic layer deposition. These findings suggest that the anisotropic electrical properties of CuPc crystallites, and their orientation with respect to the substrate, strongly affect the charge carrier injection and transport properties at the anode interface. (orig.)

  18. Phototoxic effects of free phthalocyanine and phthalocyanine conjugated to gold nanoparticles for targeted photodynamic therapy of melanoma cancer

    Science.gov (United States)

    Manoto, Sello L.; Oluwole, David O.; Malabi, Rudzani; Maphanga, Charles; Ombinda-Lemboumba, Saturnin; Nyokong, Tebello; Mthunzi-Kufa, Patience

    2017-02-01

    Photodynamic therapy (PDT) has emerged as an effective treatment modality for various malignant neoplasia and diseases. In PDT, the photochemical interaction of photosensitizer (PS), light and molecular oxygen produces singlet oxygen which can lead to tumour cell apoptosis, necrosis or autophagy. The success of PDT is limited by the hydrophobic characteristic of the PS which hinders treatment administration and efficiency. To circumvent this limitation, PS can be incorporated in nanostructured drug delivery systems such as gold nanoparticles (AuNPs). In this study, we investigated the effectiveness of free zinc monocarboxyphenoxy phthalocyanine (ZnMCPPc) and ZnMCPPc conjugated to AuNPs. Commercially purchased melanoma cancer cells cultured as cell monolayers were used in this study. Changes in cellular response were evaluated using cellular morphology, viability, proliferation and cytotoxicity. Untreated cells showed no changes in cellular morphology, proliferation and cytotoxicity. However, photoactivated free ZnMCPPc and ZnMCPPc conjugated to AuNPs showed changes in cellular morphology and a dose dependent decrease in cellular viability and proliferation as well as an increase in cell membrane. ZnMCPPc conjugated to AuNPs showed an improved efficiency in PDT as compared to free ZnMCPPc, which might be as a result of the vehicle effect of AuNPs. Both PSs used in this study were effective in inducing cell death with ZnMCPPc conjugated to AuNPs showing great potential as an effective PS for PDT.

  19. Ultraviolet-ozone-treated PEDOT:PSS as anode buffer layer for organic solar cells.

    Science.gov (United States)

    Su, Zisheng; Wang, Lidan; Li, Yantao; Zhao, Haifeng; Chu, Bei; Li, Wenlian

    2012-08-17

    Ultraviolet-ozone-treated poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)was used as the anode buffer layer in copper phthalocyanine (CuPc)/fullerene-based solar cells. The power conversion efficiency of the cells with appropriated UV-ozone treatment was found to increase about 20% compared to the reference cell. The improved performance is attributed to the increased work function of the PEDOT:PSS layer, which improves the contact condition between PEDOT:PSS and CuPc, hence increasing the extraction efficiency of the photogenerated holes and decreasing the recombination probability of holes and electrons in the active organic layers.

  20. Investigation of Organic Solar Cells Based on Donor——A ccepter Heterojunction%Investigation of Organic Solar Cells Based onDonor——A ccepter Heterojunction

    Institute of Scientific and Technical Information of China (English)

    Gao Yinhao

    2008-01-01

    The single-l ayer structure and heterojunction structure organic solar cells based on copper phthalocyanine (CuPc),3,4,9,10-Perylenetetracarboxylic dianhydride (PTCDA) and fullerene C60 were fabricated to study their photovoltaic (PV) properties. The PV performance of heterojunction structure solar cells was improved compared with the single layer structure cell.This is due to the introduction of donor-acceptor heterojunction that both expands the absorption range and offers efficient excit on dissociation site.In heterojunction structure solar cells,the PV performance of device with C60 as acceptor has highly improved because C60 has longer diffusion length o f excitons.

  1. Synthesis of mesogenic phthalocyanine-C60 donor–acceptor dyads designed for molecular heterojunction photovoltaic devices

    Directory of Open Access Journals (Sweden)

    Yves Henri Geerts

    2009-10-01

    Full Text Available A series of phthalocyanine-C60 dyads 2a–d was synthesized. Key steps in their synthesis are preparation of the low symmetry phthalocyanine intermediate by the statistical condensation of two phthalonitriles, and the final esterification of the fullerene derivative bearing a free COOH group. Structural characterization of the molecules in solution was performed by NMR spectroscopy, UV–vis spectroscopy and cyclic voltammetry. Preliminary studies suggest formation of liquid crystalline (LC mesophases for some of the prepared dyads. To the best of our knowledge, this is the first example of LC phthalocyanine-C60 dyads.

  2. Circular dichroism spectroscopic investigation of double-decker phthalocyanine with G-Quadruplex as promising telomerase inhibitor

    Science.gov (United States)

    Baǧda, Efkan; Baǧda, Esra; Yabaş, Ebru

    2017-01-01

    In the present study, interaction of a double-decker phthalocyanine with two G-quadruplex DNA, Tel 21 and cMYC, was investigated. To the best of our knowledge, this is the first study about G-quadruplex-double decker phthalocyanine interaction. The spectrophotometric titration method was used for binding constant calculations. From the binding constants, it can be said that double-decker phthalocyanine more likely to bind Tel 21 rather than cMYC. The conformational changes upon binding were monitored via circular dichroism spectroscopy. The ethidium bromide replacement assay was investigated spectrofluorometrically.

  3. A rapid safranin-metal phthalocyanine double staining technique for plants.

    Science.gov (United States)

    Achar, B N; Bhandari, J M; Urs, H G

    1993-05-01

    Pure metal 4,4',4'',4'''-tetra-substituted, sulfo-, carboxy- and nitrophthalocyanines were synthesized. Mounted, deparaffinized and partially dehydrated sections of plant tissues were stained with 0.5% safranin in 50% alcohol for 5-10 min. Excess safranin was removed with a series of 70%, 95% and absolute alcohol washes. The sections were then stained for 2-3 min using metal 4,4',4'',4'''-phthalocyanine tetracarboxylic acid (MPTC, 0.5% (V/V) containing a few drops of dilute sodium hydroxide), metal 4,4',4'',4'''-tetrasulfophthalocyanine (MPTS, 0.5% (V/V)) or metal tetranitrophthalocyanine (MPTN, 0.5% (V/V) in dimethyl sulfoxide). The sections were washed with 95%, then absolute alcohol; however, the metal tetranitrophthalocyanine section was washed only with absolute alcohol. Stained sections were treated briefly with xylene, then mounted on a coverslip. Bright peacock blue (MPTC and MPTS using Cu, Co or Ni), turquoise blue (MPTN using Cu or Ni) or parrot green (zinc phthalocyanine tetracarboxylic acid-ZnPTC, zinc phthalocyanine tetranitro derivative-ZnPTN) colors were obtained. Lignin-containing cells were stained red by safranin and the remaining cell structures were stained by the metal phthalocyanine complex with color brightness superior to that of fast green. Uniform staining, no color fading after a year, reliability, brief staining times, high color contrast (log epsilon = 4.0-4.9) and ease of use make this double staining combination ideal for routine use and photomicrography.

  4. In vivo fluorescence kinetics and localisation of aluminium phthalocyanine disulphonate in an autologous tumour model

    NARCIS (Netherlands)

    Witjes, MJH; Speelman, OC; Nikkels, PGJ; Nooren, CAAM; Nauta, JM; vanderHolt, B; vanLeengoed, HLLM; Roodenburg, JLN

    1996-01-01

    Sulphonated phthalocyanines are studied as photosensitisers for photodynamic therapy of cancer. Their strong fluorescence and tumour-localising properties make them also potentially useful for detection of cancer by fluorescence. For this purpose, we have studied the fluorescence kinetics and locali

  5. Direct observation of hindered eccentric rotation of an individual molecule : Cu-phthalocyanine on C60

    NARCIS (Netherlands)

    Stöhr, Meike; Wagner, T; Gabriel, M; Weyers, B; Moller, R

    2002-01-01

    Individual Cu-phthalocyanine molecules have been investigated by scanning tunnel microscopy on a closed packed film of C-60 at various temperatures. The molecules are found to bind asymmetrically to one C-60. While they remain in one position at low temperature, they can hop between six equivalent p

  6. Photophysical efficiency-boost of aqueous aluminium phthalocyanine by hybrid formation with nano-clays.

    Science.gov (United States)

    Staniford, Mark C; Lezhnina, Marina M; Gruener, Malte; Stegemann, Linda; Kuczius, Rauni; Bleicher, Vera; Strassert, Cristian A; Kynast, Ulrich H

    2015-09-11

    Novel organic-inorganic hybrid materials comprising nanoscaled layered silicates and native aluminium hydroxide phthalocyanine (Al(OH)Pc) allowed for the first time the exploitation of their unique photophysical properties in aqueous ambience. In particular, we were able to observe the efficient emission of Al(OH)Pc-nanoclay hybrids and generation of singlet oxygen in aqueous solution.

  7. Determination of Thermal Activation Energy and Grain Size of Iron Hexadecachloro Phthalocyanine Thin Films

    Directory of Open Access Journals (Sweden)

    Raji Koshy

    2011-01-01

    Full Text Available Electrical, structural and surface morphological properties of Iron hexadecachloro phthalocyanine thin films deposited onto glass substrates are studied as a function of post deposition annealing temperature in air. Organic semiconductors are extensively used in optical and electronic devices such as organic photovoltaic solar cells (OSC, thin film transistors (OTFT and organic light emitting diodes (OLED. Metal phthalocyanines are one of the most promising candidates to be used in the fabrication of such devices. A No. of phthalocyanines have been extensively studied. But not much work have been carried out in Cl16FePc thin films. Basic characteristics of Cl16FePc are not reported in literature. Hexadecacholoro phthalocyanines have attracted interest as possible n-type organic semiconductor with high electron mobility and good stability characteristics. In the present work we investigate the activation energy of the Cl16FePc thin films as a function of air annealing temperature. We also report the film structure and surface morphology by X-ray diffraction (XRD and Scanning electron microscopy (SEM.

  8. Strongly enhanced Raman scattering of Cu-phthalocyanine sandwiched between graphene and Au(111).

    Science.gov (United States)

    Lin, Wan-Ing; Gholami, Mohammad Fardin; Beyer, Paul; Severin, Nikolai; Shao, Feng; Zenobi, Renato; Rabe, Jürgen P

    2017-01-05

    Graphene and flat gold have both been argued to enhance Raman scattering of molecular adsorbates through a chemical mechanism. Here we show that these two effects can add to each other. For Cu-phthalocyanine in between graphene and Au(111) on mica a Raman enhancement up to 68-fold has been observed.

  9. Synthesis of phthalocyanine conjugates with gold nanoparticles and liposomes for photodynamic therapy

    CSIR Research Space (South Africa)

    Nombona, N

    2012-02-01

    Full Text Available gold nanoparticles or encapsulated in liposomes. Cell viability studies showed the optimum phototoxic effect on non-malignant cells to be 4.5 J cm-2. The PDT effect of the liposome bound phthalocyanine showed extensive damage of the breast cancer cells...

  10. Direct observation of hindered eccentric rotation of an individual molecule : Cu-phthalocyanine on C60

    NARCIS (Netherlands)

    Stöhr, Meike; Wagner, T; Gabriel, M; Weyers, B; Moller, R

    2002-01-01

    Individual Cu-phthalocyanine molecules have been investigated by scanning tunnel microscopy on a closed packed film of C-60 at various temperatures. The molecules are found to bind asymmetrically to one C-60. While they remain in one position at low temperature, they can hop between six equivalent

  11. Evidence of a Chiral Superstructure in the Discotic Mesophase of an Optically Active Phthalocyanine

    NARCIS (Netherlands)

    Nostrum, Cornelus F. van; Bosman, Anton W.; Gelinck, Gerwin H.; Picken, Stephen J.; Schouten, Pieter G.; Warman, John M.; Schouten, Arend-Jan; Nolte, Roeland J.M.

    1993-01-01

    In the liquid crystalline phase of optically active phthalocyanine (S)-1 the columns are helically distorted, as has been shown by circular dichroism experiments on a Langmuir-Blodgett film of (S)-1 and by small angle X-ray diffraction studies, and confirmed by time-resolved microwave conductivity

  12. Theoretical study of NMR, infrared and Raman spectra on triple-decker phthalocyanines

    Energy Technology Data Exchange (ETDEWEB)

    Suzuki, Atsushi; Oku, Takeo [Department of Materials Science, The University of Shiga Prefecture 2500 Hassaka, Hikone, Shiga, 522-8533 (Japan)

    2016-02-01

    Electronic structures and magnetic properties of multi-decker phthalocyanines were studied by theoretical calculation. Electronic structures, excited processes at multi-states, isotropic chemical shifts of {sup 13}C, {sup 14}N and {sup 1}H-nuclear magnetic resonance (NMR), principle V-tensor in electronic field gradient (EFG) tensor and asymmetry parameters (η), vibration mode in infrared (IR) and Raman spectra of triple-decker phthalocyanines were calculated by density functional theory (DFT) and time-dependent DFT using B3LYP as basis function. Electron density distribution was delocalized on the phthalocyanine rings with electron static potential. Considerable separation of chemical shifts in {sup 13}C, {sup 14}N and {sup 1}H-NMR was originated from nuclear spin interaction between nitrogen and carbon atoms, nuclear quadrupole interaction based on EFG and η of central metal under crystal field. Calculated optical absorption at multi-excited process was derived from overlapping π-orbital on the phthalocyanine rings. The vibration modes in IR and Raman spectra were based on in-plane deformation and stretching vibrations of metal-ligand coordination bond on the deformed structure.

  13. Magnetic fields as an investigation technique and manipulation tool for phthalocyanine molecular aggregates

    NARCIS (Netherlands)

    Boamfa, M.I.; Christianen, P.C.M.; Engelkamp, H.; Nolte, R.J.M.; Maan, J.C.

    2004-01-01

    A polarized absorption spectroscopy (PAS) study of molecular aggregate solutions of phthalocyanine molecules in high magnetic fields is presented. We show that a magnetic field can induce macroscopic ordering of molecular aggregates (MAs), in a clean, non-contact method, which is well suited for MA

  14. Nanoparticles improve biological functions of phthalocyanine photosensitizers used for photodynamic therapy.

    Science.gov (United States)

    Jia, Xiao; Jia, Lee

    2012-10-01

    Photodynamic therapy (PDT) is a new technology using photodynamic effect for disease diagnosis and treatment. It is a two-step technique involving the uptake of a photosensitizer by cancer tissue followed by light irradiation that excites the photosensitizer to produce highly reactive oxygen species, the latter execute apoptosis of cancerous cells. As a second-generation of photosensitizers, phthalocyanine demonstrates higher absorption in the 650-800 nm range and short tissue accumulation compared to their first generation. However, many potent phthalocyanine photosensitizers are hydrophobic and poorly water-soluble, which limit their therapeutic applications. As a result, advanced delivery systems and different strategies are called for to improve the effectiveness of PDT. Facts have proved that using nanoparticles as carries of photosensitizers is a very promising route. Nanoparticles have the potentials to increase photosensitizers' aqueous solubility, bioavailability and stability, and deliver photosensitizers to the target tissues. This article reviewed the commonly-used nanoparticles, including colloid gold, quantum dots, paramagnetic nanoparticles, silica-based materials, polymer-based nanoparticles, as potential delivery systems for phthalocyanine photosensitizers, and summarized the improved biological functions of phthalocyanine photosensitizers in PDT.

  15. Influence of Axial and Peripheral Ligands on the Electronic Structure of Titanium Phthalocyanines

    NARCIS (Netherlands)

    Pickup, David F.; Zegkinoglou, Ioannis; Ballesteros, Beatriz; Ganivet, Carolina R.; Garcia-Lastra, J. M.; Cook, Peter L.; Johnson, Phillip S.; Rogero, Celia; de Groot, Frank; Rubio, Angel; de la Torre, Gema; Enrique Ortega, J.; Himpsel, F. J.

    2013-01-01

    To discover how molecular changes affect the electronic structure of dye molecules for solar cells, we have investigated four titanium phthalocyanines customized by axial and peripheral ligands (monodentate oxo versus bidentate catechol and tert-butyl versus tert-butylphenoxy, respectively). X-ray a

  16. In vivo fluorescence kinetics and localisation of aluminium phthalocyanine disulphonate in an autologous tumour model

    NARCIS (Netherlands)

    Witjes, MJH; Speelman, OC; Nikkels, PGJ; Nooren, CAAM; Nauta, JM; vanderHolt, B; vanLeengoed, HLLM; Roodenburg, JLN

    1996-01-01

    Sulphonated phthalocyanines are studied as photosensitisers for photodynamic therapy of cancer. Their strong fluorescence and tumour-localising properties make them also potentially useful for detection of cancer by fluorescence. For this purpose, we have studied the fluorescence kinetics and locali

  17. Influence of axial and peripheral ligands on the electronic structure of titanium phthalocyanines

    DEFF Research Database (Denmark)

    Pickup, David F.; García Lastra, Juan Maria; Rogero, Celia

    2013-01-01

    To discover how molecular changes affect the electronic structure of dye molecules for solar cells, we have investigated four titanium phthalocyanines customized by axial and peripheral ligands (monodentate oxo versus bidentate catechol and tert-butyl versus tert-butylphenoxy, respectively). X-ra...

  18. Phthalocyanine derivatives possessing 2-(morpholin-4-yl)ethoxy groups as potential agents for photodynamic therapy.

    Science.gov (United States)

    Kucinska, Malgorzata; Skupin-Mrugalska, Paulina; Szczolko, Wojciech; Sobotta, Lukasz; Sciepura, Mateusz; Tykarska, Ewa; Wierzchowski, Marcin; Teubert, Anna; Fedoruk-Wyszomirska, Agnieszka; Wyszko, Eliza; Gdaniec, Maria; Kaczmarek, Mariusz; Goslinski, Tomasz; Mielcarek, Jadwiga; Murias, Marek

    2015-03-12

    Three 2-(morpholin-4-yl)ethoxy substituted phthalocyanines were synthesized and characterized. Phthalocyanine derivatives revealed moderate to high quantum yields of singlet oxygen production depending on the solvent applied (e.g., in DMF ranging from 0.25 to 0.53). Their photosensitizing potential for photodynamic therapy was investigated in an in vitro model using cancer cell lines. Biological test results were found particularly encouraging for the zinc(II) phthalocyanine derivative possessing two 2-(morpholin-4-yl)ethoxy substituents in nonperipheral positions. Cells irradiated for 20 min at 2 mW/cm(2) revealed the lowest IC50 value at 0.25 μM for prostate cell line (PC3), whereas 1.47 μM was observed for human malignant melanoma (A375) cells. The cytotoxic activity in nonirradiated cells of novel phthalocyanine was found to be very low. Moreover, the cellular uptake, localization, cell cycle, apoptosis through an ELISA assay, and immunochemistry method were investigated in LNCaP cells. Our results showed that the tested photosensitizer possesses very interesting biological activity, depending on experimental conditions.

  19. Femtosecond time-resolved energy transfer from CdSe nanoparticles to phthalocyanines

    Science.gov (United States)

    Dayal, S.; Królicki, R.; Lou, Y.; Qiu, X.; Berlin, J. C.; Kenney, M. E.; Burda, C.

    2006-07-01

    The first real-time observation of the early events during energy transfer from a photoexcited CdSe nanoparticle to an attached phthalocyanine molecule are presented in terms of a femtosecond spectroscopic pump-probe study of the energy transfer in conjugates of CdSe nanoparticles (NPs) and silicon phthalocyanines (Pcs) with 120 fs time resolution. Four different silicon phthalocyanines have been conjugated to CdSe NPs. All of these have proven potential for photodynamic therapy (PDT). In such NP-Pc conjugates efficient energy transfer (ET) from CdSe NPs to Pcs occurs upon selective photoexcitation of the NP moiety. Spectral analysis as well as time-resolved fluorescence up-conversion measurements revealed the structure and dynamics of the investigated conjugates. Femtosecond transient differential absorption (TDA) spectroscopy was used for the investigation of the non-radiative carrier and ET dynamics. The formation of excitons, trapped carriers states, as well as stimulated emission was monitored in the TDA spectra and the corresponding lifetimes of these states were recorded. The time component for energy transfer was found to be between 15 and 35 ps. The ET efficiencies are found to be 20-70% for the four Pc conjugates, according to fluorescence quenching experiments. Moreover, as a result of the conjugation between NP and the Pcs the photoluminescence efficiency of the Pc moieties in the conjugates do not strictly follow the quantum yields of the bare phthalocyanines.

  20. Two-dimensional multiphase behavior induced by sterically hindered conformational optimization of phenoxy-substituted phthalocyanines

    NARCIS (Netherlands)

    Samuely, Tomas; Liu, Shi-Xia; Wintjes, Nikolai; Haas, Marco; Decurtins, Silvio; Jung, Thomas A.; Stoehr, Meike

    2008-01-01

    Symmetrically substituted phthalocyanines (Pcs) with eight peripheral di-(tert-butyl)phenoxy (DTPO) groups self-organize on Ag(111) and Au(111) substrates into various assembly structures. These different structural phases were studied by scanning tunneling microscopy (STM). On the basis of

  1. Energy transfer from C-phycocyanin to phthalocyanine metal complex in reverse micelles

    Institute of Scientific and Technical Information of China (English)

    赵继全; 赵井泉; 丁西明; 蒋丽金

    1999-01-01

    A new mimic system of photosynthetic apparatus was constructed from C-phycocyanin and phthalocyanine zinc. C-PC was solubilized in the reverse micelles of non ionic surfactant Tween-80, cosurfactant pentanol, and solvent cyclohexane, in which the overall concentration of surfactant was 20% (w/v) and the mass ratio of Tween-80 to pentanol was 4:1. When the molar ratio of water to Tween-80 (Rw)≥9.0, the characteristic properties of C-PC were maintained. When it was excited, the energy transfer from C-PC to phthalocyanine zinc took place. The energy transfer efficiency was only related with the concentration of phthalocyanine, but not that of C-PC. Furthermore, the energy transfer was roughly in keeping with Perrin formulation, which indicated that the energy transfer took place approximately through dipole-dipole interaction in rigid system. The radii of the quenching sphere were calculated from the experimental results. For example, when the concentration of phthalocyanine zinc was 2.10 × 10-4 mol/

  2. Phthalocyanine-labeled LDL for tumor imaging and photodynamic therapy

    Science.gov (United States)

    Li, Hui; Marotta, Diane; Kim, Soungkyoo; Chance, Britton; Glickson, Jerry D.; Busch, Theresa M.; Zheng, Gang

    2005-01-01

    Current limitation of both near-infrared (NIR) tumor imaging and photodynamic therapy (PDT) is their lack of sufficient tumor-to-tissue contrast due to the relatively non-specific nature of delivering dye to the tumor, which has led to false negatives for NIR imaging and inadequate therapeutic ratio for PDT. Hence, agents targeting "cancer signatures", i.e. molecules that accumulate selectively in cancer cells, are particular attractive. One of these signatures is low-density-lipoprotein receptor (LDLR), which is overexpressed in many tumors. We have developed pyropheophorbide cholesterol oleate reconstituted LDL as a LDLR-targeting photosensitizer (PS) and demonstrated its LDLR-mediated uptake in vitro and in vivo. To improve the labeling efficiency for achieving high probe/protein ratio, tetra-t-butyl silicon phthalocyanine bearing two oleate moieties at its axial positions, (tBu)4SiPcBOA, was designed and synthesized. This compound was designed to 1) prevent the PS aggregation; 2) improve the PS solubility in non-polar solvent; and 3) maximize the PS binding to LDL phospholipid monolayer. Using this novel strategy, (tBu)4SiPcBOA was reconstituted into LDL (r-SiPcBOA-LDL) with a very high payload (500:1 molar ratio). In addition, (tBu)4SiPcBOA reconstituted acetylated LDL (r-SiPcBOA)-AcLDL with similar payload was also prepared. Since Ac-LDL cannot bind to LDLR, (r-SiPcBOA)-AcLDL can serve as the negative control to evaluate LDLR targeting specificity. For biological evaluation of these new agents, confocal microscopy and in vitro PDT protocols were performed using LDLR-overexpressing human hepatoblastoma G2 (HepG2) tumor model. These studies suggest that LDL serves as a delivery vehicle to bring large amount of the NIR/PDT agents selectively to tumor cells overexpressing LDLR.

  3. The photodynamic antibacterial effects of silicon phthalocyanine (Pc) 4.

    Science.gov (United States)

    Dimaano, Matthew L; Rozario, Chantal; Nerandzic, Michelle M; Donskey, Curtis J; Lam, Minh; Baron, Elma D

    2015-04-08

    The emergence of antibiotic-resistant strains in facultative anaerobic Gram-positive coccal bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA), is a global health issue. Typically, MRSA strains are found associated with institutions like hospitals but recent data suggest that they are becoming more prevalent in community-acquired infections. It is thought that the incidence and prevalence of bacterial infections will continue to increase as (a) more frequent use of broad-spectrum antibiotics and immunosuppressive medications; (b) increased number of invasive medical procedures; and (c) higher incidence of neutropenia and HIV infections. Therefore, more optimal treatments, such as photodynamic therapy (PDT), are warranted. PDT requires the interaction of light, a photosensitizing agent, and molecular oxygen to induce cytotoxic effects. In this study, we investigated the efficacy and characterized the mechanism of cytotoxicity induced by photodynamic therapy sensitized by silicon phthalocyanine (Pc) 4 on (a) methicillin-sensitive Staphylococcus aureus (MSSA) (ATCC 25923); (b) community acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) (ATCC 43300); and (c) hospital acquired methicillin-resistant Staphylococcus aureus (HA-MRSA) (PFGE type 300). Our data include confocal image analysis, which confirmed that Pc 4 is taken up by all S. aureus strains, and viable cell recovery assay, which showed that concentrations as low as 1.0 μM Pc 4 incubated for 3 h at 37 °C followed by light at 2.0 J/cm2 can reduce cell survival by 2-5 logs. These results are encouraging, but before PDT can be utilized as an alternative treatment for eradicating resistant strains, we must first characterize the mechanism of cell death that Pc 4-based PDT employs in eliminating these pathogens.

  4. The Photodynamic Antibacterial Effects of Silicon Phthalocyanine (Pc 4

    Directory of Open Access Journals (Sweden)

    Matthew L. Dimaano

    2015-04-01

    Full Text Available The emergence of antibiotic-resistant strains in facultative anaerobic Gram-positive coccal bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA, is a global health issue. Typically, MRSA strains are found associated with institutions like hospitals but recent data suggest that they are becoming more prevalent in community-acquired infections. It is thought that the incidence and prevalence of bacterial infections will continue to increase as (a more frequent use of broad-spectrum antibiotics and immunosuppressive medications; (b increased number of invasive medical procedures; and (c higher incidence of neutropenia and HIV infections. Therefore, more optimal treatments, such as photodynamic therapy (PDT, are warranted. PDT requires the interaction of light, a photosensitizing agent, and molecular oxygen to induce cytotoxic effects. In this study, we investigated the efficacy and characterized the mechanism of cytotoxicity induced by photodynamic therapy sensitized by silicon phthalocyanine (Pc 4 on (a methicillin-sensitive Staphylococcus aureus (MSSA (ATCC 25923; (b community acquired methicillin-resistant Staphylococcus aureus (CA-MRSA (ATCC 43300; and (c hospital acquired methicillin-resistant Staphylococcus aureus (HA-MRSA (PFGE type 300. Our data include confocal image analysis, which confirmed that Pc 4 is taken up by all S. aureus strains, and viable cell recovery assay, which showed that concentrations as low as 1.0 μM Pc 4 incubated for 3 h at 37 °C followed by light at 2.0 J/cm2 can reduce cell survival by 2–5 logs. These results are encouraging, but before PDT can be utilized as an alternative treatment for eradicating resistant strains, we must first characterize the mechanism of cell death that Pc 4-based PDT employs in eliminating these pathogens.

  5. Electronic properties of metal-organic and organic-organic interfaces studied by photoemission and photoabsorption spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Molodtsova, Olga

    2006-07-01

    In this work systematic studies of the organic semiconductor CuPc have been presented. In general the investigation can be devided in three parts. In the first one we have studied the electronic structure of clean CuPc thin film. The next two parts are devoted to organic-organic and metal-organic interface formation, where one of the interface components is CuPc thin film. The main results of this thesis are: - The electronic structure of the pristine organic semiconductor CuPc has been obtained by a combination of conventional and resonant photoemission, near-edge X-ray absorption, as well as by theoretical ab initio quantum-chemical calculations. The contributions of different atomic species as well as sites of the CuPc molecule to the electronic DOS has been established. A combined experimental and theoretical study of the unoccupied electronic density of states of CuPc was presented. - The electronic properties of the organic heterointerfaces between fullerite and pristine copper phthalocyanine were studied. Both interfaces, CuPc/C{sub 60} and C{sub 60}/CuPc, were found to be non-reactive with pronounced shifts of the vacuum level pointing to the formation of an interfacial dipole mainly at the CuPc side of the heterojunctions. The dipole values are close to the difference of the work functions of the two materials. Important interface parameters and hole-injection barriers were obtained. The sequence of deposition does not influence the electronic properties of the interfaces. - CuPc doped with potassium was studied by means of photoemission and photoabsorption spectroscopy. A detailed analysis of the core-level PE spectra allows one to propose possible lattice sites, which harbor the potassium ions. The films prepared in this thesis showed no finite electronic density of states at the Fermi level. - Two stages of the In/CuPc interface formation have been distinguished. The low-coverage stage is characterized by a strong diffusion of the In atoms into the

  6. Layered composites of PEDOT/PSS/nanoparticles and PEDOT/PSS/phthalocyanines as electron mediators for sensors and biosensors

    Directory of Open Access Journals (Sweden)

    Celia García-Hernández

    2016-12-01

    Full Text Available The sensing properties of electrodes chemically modified with PEDOT/PSS towards catechol and hydroquinone sensing have been successfully improved by combining layers of PEDOT/PSS with layers of a secondary electrocatalytic material such as gold nanoparticles (PEDOT/PSS/AuNPs, copper phthalocyanine (PEDOT/PSS/CuPc or lutetium bisphthalocyanine (PEDOT/PSS/LuPc2. Layered composites exhibit synergistic effects that strongly enhance the electrocatalytic activity as indicated by the increase in intensity and the shift of the redox peaks to lower potentials. A remarkable improvement has been achieved using PEDOT/PSS/LuPc2, which exhibits excellent electrocatalytic activity towards the oxidation of catechol. The kinetic studies demonstrated diffusion-controlled processes at the electrode surfaces. The kinetic parameters such as Tafel slopes and charge transfer coefficient (α confirm the improved electrocatalytic activity of the layered electron mediators. The peak currents increased linearly with concentration of catechol and hydroquinone over the range of 1.5 × 10−4 to 4.0 × 10−6 mol·L−1 with a limit of detection on the scale of μmol·L−1. The layered composite hybrid systems were also found to be excellent electron mediators in biosensors containing tyrosinase and laccase, and they combine the recognition and biocatalytic properties of biomolecules with the unique catalytic features of composite materials. The observed increase in the intensity of the responses allowed detection limits of 1 × 10−7 mol·L−1 to be attained.

  7. Photoinduced electron and energy transfer in a new porphyrin-phthalocyanine triad

    Energy Technology Data Exchange (ETDEWEB)

    Ermilov, Eugeny A. [Institut fuer Physik, Photobiophysik, Humboldt-Universitaet zu Berlin, Newtonstr. 15, D-12489 Berlin (Germany)], E-mail: ermilov@physik.hu-berlin.de; Tannert, Sebastian [Institut fuer Physik, Photobiophysik, Humboldt-Universitaet zu Berlin, Newtonstr. 15, D-12489 Berlin (Germany); Werncke, Thomas [Institut fuer Physik, Photobiophysik, Humboldt-Universitaet zu Berlin, Newtonstr. 15, D-12489 Berlin (Germany); Choi, Michael T.M. [Department of Chemistry, Chinese University of Hong Kong, Shatin, N.T., Hong Kong (China); Ng, Dennis K.P. [Department of Chemistry, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong (China)], E-mail: dkpn@cuhk.edu.hk; Roeder, Beate [Institut fuer Physik, Photobiophysik, Humboldt-Universitaet zu Berlin, Newtonstr. 15, D-12489 Berlin (Germany)

    2006-09-29

    Complexes of porphyrins, phthalocyanines, and chlorophylls are well suited for modelling both the electron and energy transfer processes in photosynthetic reaction centers and natural chlorophyll complexes. In the present paper, we report the synthesis and photophysical characterization of a novel tetraphenylporphyrin-silicon(IV) phthalocyanine triad, where two porphyrins are linked to the central silicon atom of a phthalocyanine moiety. It has been found that the photophysical properties of the triad (Tr) are strongly affected by two different types of interactions between the porphyrin (P) and the phthalocyanine (Pc) parts of Tr, namely excitation energy transfer (EET) and photoinduced electron transfer (ET). The first one results in appearance of the Pc fluorescence when the P-part was initially excited and plays dominant role in fast depopulation of the first excited singlet state of the P moiety. Another competitive process in quenching of P-part fluorescence is electron transfer, but the probability of it is six times less compared to that of EET. If the first excited singlet state of the Pc-part is populated (directly or via EET), it undergoes fast depopulation via ET to the charge-separated state. As a result, the fluorescence quantum yield of the Pc-part of Tr is approximately three orders of magnitude less compared to that of silicon(IV) phthalocyanine with two axial poly(ethylene glycol) chains (SiPc) used as a reference. Analysis of transient absorption data has shown that charge-recombination occurs with a decay time of 30 ps directly to the ground state.

  8. Heterogeneous electron transfer and oxygen reduction reaction at nanostructured iron(II) phthalocyanine and its MWCNTs nanocomposites

    CSIR Research Space (South Africa)

    Mamuru, SA

    2010-05-01

    Full Text Available Electron transfer and oxygen reduction dynamics at nanostructured iron(II) phthalocyanine/multi-walled carbon nanotubes composite supported on an edge plane pyrolytic graphite electrode (EPPGE-MWCNT-nanoFePc) platform have been reported. All...

  9. Characterization of conjugates of NaYF4:Yb,Er,Gd upconversion nanoparticle with aluminium phthalocyanines

    Science.gov (United States)

    Watkins, Zane; Uddin, Imran; Britton, Jonathan; Nyokong, Tebello

    2017-02-01

    NaYF4:Er/Yb/Gd upconversion nanoparticles (UCNP) capped with amino groups were covalently attached to chloro aluminium tetrasulphonated phthalocyanine (ClAlTSPc) and chloro aluminium tetracarboxy phthalocyanine (ClAlTCPc). The conjugates were characterized using different techniques such as infrared spectroscopy (IR), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). There was a decrease in the intensity of fluorescence emission spectra of the UCNPs at 658 nm in the presence of the phthalocyanines. This decrease indicates an energy transfer between the donor UCNP and conjugated accepting phthalocyanine (Pc), due to Förster resonance energy transfer (FRET). FRET efficiencies of 18% and 21% for ClAlTSPc and ClAlTCPc, respectively, were obtained. Oxygen generation by ClAlTSPc following FRET was proved.

  10. [Copper pathology (author's transl)].

    Science.gov (United States)

    Mallet, B; Romette, J; Di Costanzo, J D

    1982-01-30

    Copper is an essential dietary component, being the coenzyme of many enzymes with oxidase activity, e.g. ceruloplasmin, superoxide dismutase, monoamine oxidase, etc. The metabolism of copper is complex and imperfectly known. Active transport of copper through the intestinal epithelial cells involves metallothionein, a protein rich in sulfhydryl groups which also binds the copper in excess and probably prevents absorption in toxic amounts. In hepatocytes a metallothionein facilitates absorption by a similar mechanism and regulates copper distribution in the liver: incorporation in an apoceruloplasmin, storage and synthesis of copper-dependent enzymes. Metallothioneins and ceruloplasmin are essential to adequate copper homeostasis. Apart from genetic disorders, diseases involving copper usually result from hypercupraemia of varied origin. Wilson's disease and Menkes' disease, although clinically and pathogenetically different, are both marked by low ceruloplasmin and copper serum levels. The excessive liver retention of copper in Wilson's disease might be due to increased avidity of hepatic metallothioneins for copper and decreased biliary excretion through lysosomal dysfunction. Menkes' disease might be due to low avidity of intestinal and hepatic metallothioneins for copper. The basic biochemical defect responsible for these two hereditary conditions has not yet been fully elucidated.

  11. Synthesis of new polymorphs of {mu}-oxo-metal(III) phthalocyanine dimers and their photoconductive properties; {mu}-okiso-kinzoku(III) futaroshianinni ryotai no shinki kessho hentai no tansaku to denshi shashin kankotai to shiteno tokusei hyoka

    Energy Technology Data Exchange (ETDEWEB)

    Yamasaki, Y.; Kuroda, K.; Takaki, K. [Orient Chemical Industries Ltd., Osaka (Japan). I-2Group, R and D Department

    1997-12-10

    The titled {mu}-oxo-metal(III) phthalocyanine dimers were prepared and investigated their polymorphs through X-ray diffraction analysis. It was found that {mu}-oxo-aluminum phthalocyanine dimer and {mu}-oxo-gallium phthalocyanine dimer have several polymorphs, but one of the target compounds, that is {mu}-oxo-indium phthalocyanine dimer, could not be synthesized because chloroindium phthalocyanine was easily hydrolyzed through acid-pasting treatment procedure to give metal-free phthalocyanine. The characterization of these compounds by the several chemical analytical methods was satisfied for the target molecules and the FD-Mass analysis distinguished clearly between the hydroxymetal phthalocyanine and the corresponding phthalocyanine dimer. We also studied their photoconductive properties on the bilayer photoreceptor consisted of the above phthalocyanine dimer as the charge generating material. It was found that the specific polymorphs of {mu}-oxo-metal(III) phthalocyanine dimers have good photoconductive properties: the APL-II(the II type of {mu}-oxo-Al(III) phthalocyanine dimer discussed in this article) has a good spectral response of the photosensitivity in the shorter wavelength, and the GPL-G (the G type of {mu}-oxo-Ga(III) phthalocyanine dimer discussed in this article) has a fairly high photosensitivity in the wavelength region of laser diode light wavelength, compared with the common phthalocyanine photoreceptors. 14 refs., 9 figs., 3 tabs.

  12. Supramolecular Structure, Physical Properties, and Langmuir-Blodgett Film Formation of an Optically Active Liquid-Crystalline Phthalocyanine

    NARCIS (Netherlands)

    Nostrum, Cornelus F. van; Bosman, Anton W.; Gelinck, Gerwin H.; Schouten, Pieter G.; Warman, John M.; Devillers, Marinus A.C.; Meijerink, Andries; Picken, Stephen J.; Sohling, Ulrich; Schouten, Arend-Jan; Nolte, Roeland J.M.

    1995-01-01

    The structure and physical properties of optically active, metal-free 2,3,9,10,16,17,23,24-octa(S-3,7-dimethyloctoxy)phthalocyanine ((S)-Pc(8,2)) are reported and compared with those of the phthalocyanine with (R,S) side chains (mixture of 43 stereoisomers). Unlike the latter compound, (S)-Pc(8,2) l

  13. Photophysical and photochemical studies of a novel amphiphilic zinc phthalocyanine and its interaction with calf thymus DNA

    Science.gov (United States)

    Yuan, Linxin; Gui, Li; Wang, Yue; Zhang, Quanquan; Zhou, Lin; Wei, Shaohua

    2016-04-01

    β-tetra (aminophenoxy) sulfonic substituted zinc phthalocyanines (SNZnPc), a novel amphiphilic zinc phthalocyanine (Pc), was synthesized. The photophysical, photochemical, and photobiology properties were studied. Results indicated that the synthesized SNZnPc has good amphiphilic property and high reactive oxygen species (ROSs) generation ability. Furthermore, SNZnPc has strong affinity to calf thymus DNA (CT-DNA) through intercalation ways and can effectively cleavage CT-DNA after irradiation by light with appropriate wavelength.

  14. Photophysical and photochemical studies of a novel amphiphilic zinc phthalocyanine and its interaction with calf thymus DNA.

    Science.gov (United States)

    Yuan, Linxin; Gui, Li; Wang, Yue; Zhang, Quanquan; Zhou, Lin; Wei, Shaohua

    2016-04-05

    β-tetra (aminophenoxy) sulfonic substituted zinc phthalocyanines (SNZnPc), a novel amphiphilic zinc phthalocyanine (Pc), was synthesized. The photophysical, photochemical, and photobiology properties were studied. Results indicated that the synthesized SNZnPc has good amphiphilic property and high reactive oxygen species (ROSs) generation ability. Furthermore, SNZnPc has strong affinity to calf thymus DNA (CT-DNA) through intercalation ways and can effectively cleavage CT-DNA after irradiation by light with appropriate wavelength.

  15. Electronic structure differences between H(2)-, Fe-, Co-, and Cu-phthalocyanine highly oriented thin films observed using NEXAFS spectroscopy.

    Science.gov (United States)

    Willey, T M; Bagge-Hansen, M; Lee, J R I; Call, R; Landt, L; van Buuren, T; Colesniuc, C; Monton, C; Valmianski, I; Schuller, Ivan K

    2013-07-21

    Phthalocyanines, a class of macrocyclic, square planar molecules, are extensively studied as semiconductor materials for chemical sensors, dye-sensitized solar cells, and other applications. In this study, we use angular dependent near-edge x-ray absorption fine structure (NEXAFS) spectroscopy as a quantitative probe of the orientation and electronic structure of H2-, Fe-, Co-, and Cu-phthalocyanine molecular thin films. NEXAFS measurements at both the carbon and nitrogen K-edges reveal that phthalocyanine films deposited on sapphire have upright molecular orientations, while films up to 50 nm thick deposited on gold substrates contain prostrate molecules. Although great similarity is observed in the carbon and nitrogen K-edge NEXAFS spectra recorded for the films composed of prostrate molecules, the H2-phthalocyanine exhibits the cleanest angular dependence due to its purely out-of-plane π* resonances at the absorption onset. In contrast, organometallic-phthalocyanine nitrogen K-edges have a small in-plane resonance superimposed on this π* region that is due to a transition into molecular orbitals interacting with the 3dx(2)-y(2) empty state. NEXAFS spectra recorded at the metal L-edges for the prostrate films reveal dramatic variations in the angular dependence of specific resonances for the Cu-phthalocyanines compared with the Fe-, and Co-phthalocyanines. The Cu L3,2 edge exhibits a strong in-plane resonance, attributed to its b1g empty state with dx(2)-y(2) character at the Cu center. Conversely, the Fe- and Co- phthalocyanine L3,2 edges have strong out-of-plane resonances; these are attributed to transitions into not only b1g (dz(2)) but also eg states with dxz and dyz character at the metal center.

  16. Investigation of structural, optical and electrical properties of a new cobalt phthalocyanine thin films with potential applications in perchlorate sensor

    OpenAIRE

    Braik, Mohammed; Dridi, C.; Ali, A.; Ben Ali, M.; Abbas, Mohammad Nooredeen; Errachid, Abdelhamid

    2015-01-01

    International audience; Optical, structural and electrical properties of new cobalt phthalocyanine derivatives (Co(II)Pc-AP) thin films have been investigated. The Raman spectroscopy study shows the different vibrations bands corresponding to the metallophthalocyanine. The cobalt-phthalocyanine derivative films exhibit absorption spectra with a resolved electronic structure in the UV-vis range and the energy gap was determined by the Tauc method. Electrical properties of the ITO/Co(II)Pc-AP/A...

  17. Supramolecular Structure, Physical Properties, and Langmuir-Blodgett Film Formation of an Optically Active Liquid-Crystalline Phthalocyanine

    NARCIS (Netherlands)

    Nostrum, Cornelus F. van; Bosman, Anton W.; Gelinck, Gerwin H.; Schouten, Pieter G.; Warman, John M.; Devillers, Marinus A.C.; Meijerink, Andries; Picken, Stephen J.; Sohling, Ulrich; Schouten, Arend-Jan; Nolte, Roeland J.M.

    1995-01-01

    The structure and physical properties of optically active, metal-free 2,3,9,10,16,17,23,24-octa(S-3,7-dimethyloctoxy)phthalocyanine ((S)-Pc(8,2)) are reported and compared with those of the phthalocyanine with (R,S) side chains (mixture of 43 stereoisomers). Unlike the latter compound, (S)-Pc(8,2) l

  18. [Copper IUDs (author's transl)].

    Science.gov (United States)

    Thiery, M

    1983-10-01

    Following initial development of the Grafenberg ring in the 1920's, IUDs fell into disuse until the late 1950s, when plastic devices inserted using new technology began to gain worldwide acceptance. Further research indicated that copper had a significant antifertility effect which increased with increasing surface area, and several copper IUDs were developed and adapted, including the Copper T 200, the Copper T 220C, and the Copper T 380 A, probably the most effective yet. The Gravigard and Multiload are 2 other copper devices developed according to somewhat different principles. Copper devices are widely used not so much because of their great effectiveness as because of their suitability for nulliparous patients and their ease of insertion, which minimizes risk of uterine perforation. Records of 2584 women using Copper IUDs for 7190 women-years and 956 women using devices without copper for 6059 women-years suggest that the copper devices were associated with greater effectiveness and fewer removals for complications. Research suggests that the advantages of copper IUDs become more significant with increased duration of use. Contraindications to copper devices include allergy to copper and hepatolenticular degeneration. No carcinogenic or teratogenic effect of copper devices has been found, but further studies are needed to rule out other undesirable effects. Significant modifications of copper devices in recent years have been developed to increase their effectiveness, prolong their duration of usefulness, facilitate insertion and permit insertion during abortion or delivery. The upper limit of the surface area of copper associated with increased effectiveness appears to be between 200-300 sq mm, and at some point increases in copper exposure may provoke expulsion of the IUD. The duration of fertility inhibition of copper IUDs is usually estimated at 2-3 years, but recent research indicates that it may be 6-8 years, and some devices may retain copper surface

  19. Effects of central metal on electronic structure, magnetic properties, infrared and Raman spectra of double-decker phthalocyanine

    Science.gov (United States)

    Suzuki, Atsushi; Oku, Takeo

    2016-09-01

    The effects of the central metal in double-decker metal phthalocyanine on the electronic structure, magnetic properties, and infrared and Raman spectra of the complex were investigated. Electron density distributions were delocalized on the phthalocyanine rings. The narrow energy gap and infrared peaks observed in the ultra-violet-visible-near infrared spectra of the systems were attributed to phthalocyanine ring-ring interactions the between overlapping π-orbitals on each ring. The chemical shift behavior of the phthalocyanine rings was separated by the deformation of their structure owing to nuclear magnetic interaction of the nuclear quadrupole interaction as determined by the electronic field gradient and asymmetric parameters. The magnetic parameters of principle g-tensors were dependent on the perturbation of the crystal field by the hybridization of the d-spin in the central metal conjugated with nitrogen ligands. In the case of the vanadyl system, the IR vibration modes were shifted by the soft vibration mode for resolving the symmetrical structure. Inactive Raman vibration modes arose from no-polarization on the phthalocyanine rings. Double-decker metal phthalocyanines have great advantages for the control of the magnetic mechanism for quantum spin entanglement in the relaxation process.

  20. Investigation of interaction between alkoxy substituted phthalocyanines with different lengths of alkyl residue and bovine serum albumin

    Energy Technology Data Exchange (ETDEWEB)

    Lebedeva, Natalya Sh., E-mail: nsl@isc-ras.ru [G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences, Akademicheskaya, 1, 153045 Ivanovo (Russian Federation); Gubarev, Yury A.; Vyugin, Anatoly I. [G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences, Akademicheskaya, 1, 153045 Ivanovo (Russian Federation); Koifman, Oscar I. [Research Institute of Macroheterocycles of Ivanovo State University of Chemistry and Technology, 153000 Ivanovo (Russian Federation)

    2015-10-15

    Interaction between bovine serum albumin and alkoxy substituted phthalocyanines was studied by means of electron absorption spectroscopy, fluorescence spectroscopy and viscosimetry. The binding constants and binding distance were calculated. It was found that ZnPc(4-NH-CO-C{sub 6}H{sub 4}-OC{sub 10}H{sub 21}){sub 4} prevents twisting of BSA molecule and localizes between subdomains IB and IIA in protein globule. ZnPc(4-NH-CO-C{sub 6}H{sub 4}-OC{sub 6}H{sub 13}){sub 4} and ZnPc(4-NH-CO-C{sub 6}H{sub 4}-OC{sub 8}H{sub 17}){sub 4} are located on the outer surface of the protein globule. In the case of ZnPc(4-NH-CO-C{sub 6}H{sub 4}-OC{sub 3}H{sub 7}){sub 4} it can be assumed that the phthalocyanine molecule is in the immediate vicinity of the subdomains IB and IIA. - Highlights: • Interaction between bovine serum albumin and alkoxy substituted phthalocyanines was studied by means of electron absorption spectroscopy, fluorescence spectroscopy and viscosimetry. • The binding constants and binding distance were calculated by using the Scatchard method. • Photochemical characteristics of phthalocyanines of studied phthalocyanines are defined. • Localization of phthalocyanines on the protein globule is defined.

  1. Water soluble peripheral and non-peripheral tetrasubstituted zinc phthalocyanines: Synthesis, photochemistry and bovine serum albumin binding behavior

    Energy Technology Data Exchange (ETDEWEB)

    Çakır, Volkan; Çakır, Dilek [Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey); Pişkin, Mehmet [Department of Food Technology, Çanakkale Vocational School of Technical Sciences, Çanakkale Onsekiz Mart University, 17100 Çanakkale (Turkey); Durmuş, Mahmut [Gebze Institute of Technology, Department of Chemistry, PO Box 141, Gebze 41400, Kocaeli (Turkey); Bıyıklıoğlu, Zekeriya, E-mail: zekeriya_61@yahoo.com [Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey)

    2014-10-15

    The new peripherally and non-peripherally tetra-1,3-bis[3-(diethylamino)phenoxy]propan-2-ol substituted zinc(II) phthalocyanine complexes (2a and 3a) and their quaternized amphiphilic derivatives (2b and 3b) have been synthesized and characterized using UV–vis, FT-IR, {sup 1}H-NMR, {sup 13}C-NMR, MS spectroscopic data and elemental analysis for the first time. The quaternized complexes (2b and 3b) show excellent solubility in water and DMSO which makes them potential photosensitizers for use in photodynamic therapy (PDT) of cancer. The photochemical (singlet oxygen generation and photodegradation under light irradiation) properties of these novel phthalocyanines are investigated in dimethylsulfoxide (DMSO) for non-quaternized complexes and in DMSO, phosphate buffered solution (PBS) or PBS+triton X-100 (TX) solution for quaternized complexes. In this study, the effects of the aggregation of the molecules, quaternization, position of the substituents (peripherally or non-peripherally) and nature of the solvents (DMSO, PBS or PBS+triton X-100) on the photochemical parameters of the zinc (II) phthalocyanines are also reported. In addition, a spectroscopic investigation of the binding behavior of the quaternized zinc(II) phthalocyanine complexes to bovine serum albumin (BSA) is also presented in this work. - Highlights: • Synthesis of zinc phthalocyanines is performed. • Photophysical and photochemical properties of phthalocyanines are studied. • Photodynamic therapy studies are performed.

  2. THIN FILM-BASED SENSOR FOR MOTOR VEHICLE EXHAUST GAS, NH3, AND CO DETECTION

    Directory of Open Access Journals (Sweden)

    S. Sujarwata

    2016-10-01

    Full Text Available A copper phthalocyanine (CuPc thin film based gas sensor with FET structure and channel length 100 μm has been prepared by VE method and lithography technique to detect NH3, motor cycle exhaust gases and CO. CuPc material layer was deposited on SiO2 by the vacuum evaporator (VE method at room temperature and pressure of 8 x10-4 Pa. The stages of manufacturing gas sensor were Si/SiO2 substrate blenching with ethanol in an ultrasonic cleaner, source, and drain electrodes deposition on the substrate by using a vacuum evaporator, thin film deposition between the source/drain and gate deposition. The sensor response times to NH3, motorcycle exhaust gases and CO were 75 s, 135 s, and 150, respectively. The recovery times were 90 s, 150 s and 225, respectively. It is concluded that the CuPc thin film-based gas sensor with FET structure is the best sensor to detect the NH3 gas.Sensor gas berbasis film tipis copper phthalocyanine (CuPc berstruktur FET dengan panjang channel 100 μm telah dibuatdengan metode VE dan teknik lithography untuk mendeteksi NH3 gas buang kendaraan bermotor dan CO. Lapisan bahan CuPc dideposisikan pada permukaan silikon dioksida (SiO2 dengan metode vacuum evaporator (VE pada temperatur ruang dengan tekanan 8 x10-4 Pa. Tahapan pembuatan sensor gas adalah pencucian substrat Si/SiO2 dengan etanol dalam ultrasonic cleaner, deposisi elektroda source dan drain di atas substrat dengan metode vacuum evaporator, deposisi film tipis diantara source/drain dan deposisi gate. Waktu tanggap sensor terhadap NH3, gas buang kendaraan bermotor dan CO berturut-turut adalah 75 s, 135 s,dan 150 s. Waktu pemulihan berturut-turut adalah 90 s, 150 s,dan 225 s. Disimpulkan bahwa sensor gas berstruktur FET berbasis film tipis CuPc merupakan sensor paling baik untuk mendeteksi adanya gas NH3.

  3. Review Article: Structures of phthalocyanine molecules on surfaces studied by STM

    Directory of Open Access Journals (Sweden)

    Yongfeng Wang

    2012-12-01

    Full Text Available This review mainly focuses on progress recently achieved in the growth of phthalocyanine molecules on single-crystal surfaces of sub-monolayer up to few-monolayer thin films studied by scanning tunneling microscopy in our groups. On metallic surfaces such as Au(111, Ag(111 and Cu(111, molecular superstructures are determined by combining directional intermolecular interactions caused by symmetry reduction, molecule-substrate interactions and indirect long-range interactions due to quantum interference of surface state electrons. On semiconducting TiO2 surface, molecular assembling structures are dictated by the strong molecule-substrate interaction. However, on insulating NaCl film, molecule-molecule interaction dominates over the molecule-NaCl coupling, leading to molecular growth behavior. Knowledge obtained from these studies would help people better understand the physicochemical properties of the phthalocyanine molecules at surfaces so that their new applications could be further explored and uncovered in the future.

  4. Optical spectra of phthalocyanines and related compounds a guide for beginners

    CERN Document Server

    Isago, Hiroaki

    2015-01-01

    This book displays how optical (absorption, emission, and magnetic circular dichroism) spectra of phthalocyanines and related macrocyclic dyes can be varied from their prototypical ones depending on conditions. As these compounds can be involved in colorful chemistry (which might be driven by impurities in solvents), their spectra behave like the sea-god Proteus in their mutability. Therefore, those who have been engaged with phthalocyanines for the first time, including even educated professional researchers and engineers, may have been embarrassed by the deceptive behavior of their compounds and could have, in the worst cases, given up their projects. This book is aimed not merely at reviewing the optical spectra, but also at helping such people, particularly beginners, to figure them out by showing some examples of their prototypical spectra and their variations in several situations. For the purpose of better understanding, the book also provides an introduction to their theoretical backgrounds as graphic...

  5. Preparation and magnetic properties of phthalocyanine-based carbon materials containing transition metals

    Science.gov (United States)

    Honda, Z.; Sato, S.; Hagiwara, M.; Kida, T.; Sakai, M.; Fukuda, T.; Kamata, N.

    2016-07-01

    A simple method for the preparation of bulk quantities of magnetic carbon materials, which contain uniformly dispersed transition metals (M = Fe, Co, Ni, and Cu) as the magnetic components, is presented. By using highly chlorinated metal phthalocyanine as the building block and potassium as the coupling reagent, phthalocyanine-based carbon materials (PBCMs) containing transition metals were obtained. Our experiments demonstrate the structure of these PBCMs consists of transition metals embedded in graphitic carbon that includes a square planar MN4 magnetic core and the Fe and Co-PBCM possess spontaneous magnetization at room temperature. In addition, carbon-coated transition metal particles were obtained by the Wurtz-type reaction with excess amount of potassium coupling agent. The large transition metal surface area and magnetization of these M-PBCMs are useful for spintronic and catalytic applications.

  6. Phthalocyanine-Biomolecule Conjugated Photosensitizers for Targeted Photodynamic Therapy and Imaging.

    Science.gov (United States)

    Iqbal, Zafar; Chen, Jincan; Chen, Zhuo; Huang, Mingdong

    2015-01-01

    Photodynamic therapy (PDT) is now in clinical practice in many European and American countries as a minimally invasive therapeutic technique to treat oncologic malignancies and other nononcologic conditions. Phthalocyanines (Pcs) are gathering importance as effective photosensitizers in targeted PDT and imaging of tumors. The possibility of modification around the Pc macrocycle led the researchers to the synthesis of a diversity of photosensitizers with varied cell specificity, cellular internalization and localization, photodynamic cytotoxicity and excretion. Cellular targeting is the primary aspect of an ideal photosensitizer for targeting PDT. Therefore, Pcs have been structurally modified with a variety of biomolecules capable of recognizing the specific lesions. This review emphasizes the photocytotoxicity and the cellular uptakes of phthalocyanine photosensitizers conjugated with biomolecules including carbohydrates, nucleotides and protein constituents such as amino acids and peptides. In addition, the role of the Pc-biomolecule conjugates in imaging and antimicrobial chemotherapy has been discussed.

  7. Electronic structures and magnetic/optical properties of metal phthalocyanine complexes

    Energy Technology Data Exchange (ETDEWEB)

    Baba, Shintaro; Suzuki, Atsushi, E-mail: suzuki@mat.usp.ac.jp; Oku, Takeo [Department of Materials Science, The University of Shiga Prefecture. 2500 Hassaka, Hikone, Shiga 522-8533 (Japan)

    2016-02-01

    Electronic structures and magnetic / optical properties of metal phthalocyanine complexes were studied by quantum calculations using density functional theory. Effects of central metal and expansion of π orbital on aromatic ring as conjugation system on the electronic structures, magnetic, optical properties and vibration modes of infrared and Raman spectra of metal phthalocyanines were investigated. Electron and charge density distribution and energy levels near frontier orbital and excited states were influenced by the deformed structures varied with central metal and charge. The magnetic parameters of chemical shifts in {sup 13}C-nuclear magnetic resonance ({sup 13}C-NMR), principle g-tensor, A-tensor, V-tensor of electric field gradient and asymmetry parameters derived from the deformed structures with magnetic interaction of nuclear quadruple interaction based on electron and charge density distribution with a bias of charge near ligand under crystal field.

  8. Porous Azo-Bridged Porphyrin-Phthalocyanine Network with High Iodine Capture Capability.

    Science.gov (United States)

    Li, Hui; Ding, Xuesong; Han, Bao-Hang

    2016-08-08

    We report a highly efficient iodine adsorbent achieved by rational design of a porous azo-bridged porphyrin-phthalocyanine network (AzoPPN), which was synthesized by a catalyst-free coupling reaction between free-base 5,10,15,20-tetrakis(4-nitrophenyl)-porphyrin and nickel tetraaminophthlocyanine. AzoPPN has a permanent porous structure and plenty of porphyrin and phthalocyanine units in the skeleton as effective sorption sites. It displays excellent adsorption of iodine vapor up to 290 wt. % and also shows remarkable capability as adsorbent for iodine in solution. This strategy of combining physisorption with chemisorption in one adsorbent will pave the way for the development of new materials for iodine capture. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Chemically robust fluoroalkyl phthalocyanine-oligonucleotide bioconjugates and their GRP78 oncogene photocleavage activity.

    Science.gov (United States)

    Patel, Pradeepkumar; Patel, Hemantbhai H; Borland, Emily; Gorun, Sergiu M; Sabatino, David

    2014-06-18

    The first representative of functionalized fluoroalkyl phthalocyanines, F48H7(COOH)PcZn, is reported. The complex generates (1)O2 affording long-lasting photooxidation of an external substrate without self-decomposition. The carboxylic group couples with an antisense oligonucleotide targeting GRP78 oncogenes, resulting in the F48H7PcZn-cancer targeting oligonucleotide (CTO). The bioconjugated fluorophthalocyanine effectively hybridizes complementary GRP78 DNA and mRNA sequences. Piperidine cleavage assays reveal desired photochemical oligonucleotide oxidative degradation for both F48H7PcZn-CTO:DNA and F48H7PcZn-CTO:mRNA hybrids. This new materials strategy could be extended to other functional fluorinated phthalocyanines-antisense oligonucleotide combinations for long-lasting oncogene-targeting photodynamic therapy.

  10. Bridged Phthalocyanine Systems for Sensitization of Nanocrystalline TiO2 Films

    Directory of Open Access Journals (Sweden)

    Gloria Zanotti

    2010-01-01

    Full Text Available Phthalocyanines based-dyes represent attractive alternatives to the expensive and polluting pyridyl based Ru complexes because of their photochemical and thermal stability, they do show in fact intense absorption in the UV/blue (Soret band and the red/near IR (Q band spectral regions and appear very promising as sensitizer dyes for DSSC. In this contribution we review the state of the art and the recent progress in the application of these materials as dyes for DSSC and present three new dyes which are bridged derivatives of Iron phthalocyanine. Synthesis, optical properties, electrochemical characterization and device performances are discussed with regard to the different substitution degree of the macrocycle.

  11. Synthesis, spectral properties of aluminum polymeric phthalocyanine carboxyl with low aggregation in aqueous solution

    Institute of Scientific and Technical Information of China (English)

    ZHAO Peng; NIU LiHong; ZHONG Cheng; DONG SiDa; ZHANG FuShi

    2008-01-01

    A water soluble poly-[tetrakis-(2,3-dicarboxylate phenoxy) methyl methan] aluminum phthalocyanine (AIPPc.(COOH)x) has been synthesized from the cyclization of tetranuclear phthalonitrile and succes-sive hydrolysis of cyano in alkaline solution. The absorption spectra showed low aggregation of this compound in Ph 9.18 buffer than that of existing water soluble phthalocyanine compounds. With the addition of Triton X 100, an enhancement of fluorescence emission with quantum yield from 0.4 to 0.83 was observed; contrarily, it was thoroughly quenched by the addition of CATB in suit. A longer life time of singlet state was also detected in presence of Triton X 100. The result indicates that AIPPc,(COOH)x is desired to investigate in fluorescent probe or in fluorescence imaging diagnose.

  12. Phthalocyanine and azaphthalocyanines containing eugenol: synthesis, DNA interaction and comparison of lipase inhibition properties

    Indian Academy of Sciences (India)

    GÜNAY KAYA KANTAR; ÖZLEM FAİZ; ONUR ŞAHİN; SELAMİ ŞAŞMAZ

    2017-08-01

    Novel eugenol-substituted zinc(II) azaphthalocyanines (ZnAzaPcs)were synthesised and their lipase inhibition and DNA binding properties compared with phthalocyanines (Pcs) containing eugenol. This is the first study on lipase inhibition and DNA binding of Pcs and AzaPcs containing a pharmacophore group, such as eugenol. The novel ZnAzaPcs were characterised using a combination of FT-IR, ¹HNMR, ¹³CNMR, UV–Vis, MS and elemental analysis. The crystal structures of two pyrazine compounds were also determined by the single crystal diffraction technique. This study showed that two phthalocyanines compounds (3a and 4a) could be potential lipase inhibitor agents due to greater hydrophobicity than other azaphtalocyanines. Compound 4a displayed lowest IC₅₀ value. Non-intercalative binding to DNA was identified only for compound 2a.

  13. Novel axially carborane-cage substituted silicon phthalocyanine photosensitizer; synthesis, characterization and photophysicochemical properties

    Science.gov (United States)

    Atmaca, Göknur Yaşa; Dizman, Cemil; Eren, Tarık; Erdoğmuş, Ali

    2015-02-01

    The novel axially dicarborane substituted silicon (IV) (SiPc-DC) phthalocyanine was synthesized by treating silicon phthalocyanine dichloride SiPc(Cl)2 (SiPc) with o-Carborane monool. The compound was characterized by mass spectrometry, UV-Vis, FT-IR, 1H and 11B Nuclear Magnetic Resonance Spectroscopy (NMR). Spectral, photophysical (fluorescence quantum yield) and photochemical (singlet oxygen (ΦΔ) and photodegradation quantum yield (Φd)) properties of the complex were reported in different solutions (Dimethyl sulfoxide (DMSO), Dimethylformamide (DMF) and Toluene). The results of spectral measurements showed that both SiPc and carborane cage can have potential to be used as sensitizers in photodynamic therapy (PDT) and boron neutron capture therapy (BNCT) by their singlet oxygen efficiencies (ΦΔ = 0.41, 0.39).

  14. Effects of iron phthalocyanine on performance of MH/Ni battery

    Institute of Scientific and Technical Information of China (English)

    王芳; 吴锋

    2004-01-01

    Oxygen evolution causes a high inner pressure during charge and overcharge for MH/Ni battery, and an inappropriate eliminating way of the oxygen in the battery results in accumulation of heat. This is the main obstacle to develop and apply high capability and high power battery. How to reduce the ratio of the chemical catalysis rate to the electric catalysis rate in MH/Ni battery is considered as an urgent question. Iron phthalocyanine(FePc) was chosen as an electrochemical catalyst. The batteries were prepared by adding iron phthalocyanine with different dosages. The inner pressure, the capacity attenuation, the discharge voltage and capacity at high current of these three batteries were compared. The battery with 1 mg FePc in the negative electrode exhibits a good performance.

  15. Phthalocyanine identification in paintings by reflectance spectroscopy. A laboratory and in situ study

    Science.gov (United States)

    Poldi, G.; Caglio, S.

    2013-06-01

    The importance of identifying pigments using non invasive (n.i.) analyses has gained increasing importance in the field of spectroscopy applied to art conservation and art studies. Among the large set of pigments synthesized and marketed during 20th century, surely phthalocyanine blue and green pigments occupy an important role in the field of painting (including restoration) and printing, thanks to their characteristics like brightness and fastness. This research focused on the most used phthalocyanine blue (PB15:1 and PB15:3) and green pigments (PG7), and on the possibility to identify these organic compounds using a methodology like reflectance spectroscopy in the UV, visible and near IR range (UV-vis-NIR RS), performed easily through portable instruments. Laboratory tests and three examples carried out on real paintings are discussed.

  16. Synthesis and electrochemical and photophysical studies of tetrathiafulvalene-annulated phthalocyanines.

    Science.gov (United States)

    Loosli, Claudia; Jia, Chunyang; Liu, Shi-Xia; Haas, Marco; Dias, Marylène; Levillain, Eric; Neels, Antonia; Labat, Gael; Hauser, Andreas; Decurtins, Silvio

    2005-06-24

    The synthesis of tetrakis(tetrathiafulvalene)-annulated metal-free and metallophthalocyanines 5-8 via the tetramerization of the phthalonitrile derivative 4 is reported. All of them have been fully characterized by electronic absorption spectroscopy, thin-layer cyclic voltammetry, mass spectrometry, and elemental analysis. Their solution electrochemical data show two reversible four-electron oxidation waves, indicating that these fused systems are strong pi-electron donors, which give rise to tetra- or octaradical cation species. For the metal-free phthalocyanine 5, additionally a reversible one-electron wave was found in the negative direction arising from the reduction of the macrocycle. Moreover, the tetrathiafulvalene unit acts as an efficient reductive electron-transfer quencher for the phthalocyanine emission, but upon its oxidation, an intense luminescence is switched on.

  17. Novel azobenzene-phthalocyanine dyads——design of photo-modulated J-aggregation

    Institute of Scientific and Technical Information of China (English)

    NIU LiHong; ZHONG Cheng; CHEN ZiHui; ZHANG Zhi; LI ZhongYu; ZHANG FuShi; TANG YingWu

    2009-01-01

    Based on the J-aggregation mechanism of α-aryl/alkoxy-subetituted zinc phthalocyanines(Pcs) in non-coordinating solvents, two novel azobenzene-phthalocyanine dyads (3-azo-ZnPc and 4-azo-ZnPc) were synthesized with the aim of developing Pc compounds whose ability to form J-aggregation could be photo-modulated. It was found that 3-azo-ZnPc in chloroform could be effectively photo-controlled in a wide range. This phenomenon could be explained by the changes in the geometry and dipole moment of azobenzene during the photo-isomerization process. 4-azo-ZnPc did not have this ability at all, with or without UV light illumination. The positions of the oxygen atoms to which the aryl/alkoxy substitution was attached relatively were found important in determining the aggregation ability.

  18. Polymeric complex micelle loaded with axially substituted silicon(Ⅳ) phthalocyanine

    Institute of Scientific and Technical Information of China (English)

    Bao Quan Huang

    2009-01-01

    A novel axially substituted silicon(IV) phthalocyanine,namely di-pyridyloxy axially substituted silicon(Ⅳ) phthalocyanine 2 was synthesized and characterized by UV/vis,IR,elemental analysis,MS as well as 1H NMR spectroscopy.Hydrophobic 2 was encapsulated by amphiphilic triblock copolymer poly[Nε-(benzyloxycarbonyl-lysine]-poly(ethylene glycol)-poly [Nε-(benzyl oxycarbonyl) (PLL(Z)-b-PEG-b-PLL(Z)) to form hydrophobic 2-loaded polymeric complex miceile (PIC) (2-loaded PIC).Atom force microscopy (AFM) image showed that 2-loaded PIC formed a spherical nanocarrier with approximately 35-50 nm in diameter.The fluorescence intensity and lifetime of 2-loaded PIC was significantly enhanced by the incorporation 2 into PIC nanocarrier.

  19. Handling of Copper and Copper Oxide Nanoparticles by Astrocytes.

    Science.gov (United States)

    Bulcke, Felix; Dringen, Ralf

    2016-02-01

    Copper is an essential trace element for many important cellular functions. However, excess of copper can impair cellular functions by copper-induced oxidative stress. In brain, astrocytes are considered to play a prominent role in the copper homeostasis. In this short review we summarise the current knowledge on the molecular mechanisms which are involved in the handling of copper by astrocytes. Cultured astrocytes efficiently take up copper ions predominantly by the copper transporter Ctr1 and the divalent metal transporter DMT1. In addition, copper oxide nanoparticles are rapidly accumulated by astrocytes via endocytosis. Cultured astrocytes tolerate moderate increases in intracellular copper contents very well. However, if a given threshold of cellular copper content is exceeded after exposure to copper, accelerated production of reactive oxygen species and compromised cell viability are observed. Upon exposure to sub-toxic concentrations of copper ions or copper oxide nanoparticles, astrocytes increase their copper storage capacity by upregulating the cellular contents of glutathione and metallothioneins. In addition, cultured astrocytes have the capacity to export copper ions which is likely to involve the copper ATPase 7A. The ability of astrocytes to efficiently accumulate, store and export copper ions suggests that astrocytes have a key role in the distribution of copper in brain. Impairment of this astrocytic function may be involved in diseases which are connected with disturbances in brain copper metabolism.

  20. Phthalocyanine-nanocarbon ensembles: From discrete molecular and supramolecular systems to hybrid nanomaterials

    OpenAIRE

    Bottari, Giovanni; De La Torre, Gema; Torres, Tomas

    2015-01-01

    This document is the Accepted Manuscript version of a Published Work that appeared in final form in Accounts of Chemical Research, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/ar5004384 Conspectus Phthalocyanines (Pcs) are macrocyclic and aromatic compounds that present unique electronic features such as high molar absorption coefficients, rich redox chemistry, and...

  1. Nonlinear Optical Properties of Indium Phthalocyanine Axially Grafted Polystyrene Thin Film

    Institute of Scientific and Technical Information of China (English)

    ZHU Rong-Yi; QIU Xue-Qiong; CHEN Yu; QIAN Shi-Xiong

    2006-01-01

    @@ Ultrafast dynamics and third-order nonlinearity of thin films of tert-butyl peripherally-substituted indium ph thalocyanine axially grafted polystyrene (tBu4PcIn-PS) are investigated by femtosecond optical-Kerr-effect (OKE) and z-scan experiments. The fastest component (< 200 fs) in the OKE traces of the film is related to the electron cloud distortion, where the phthalocyanine-polymer interaction may enhance this contribution.

  2. Electrochemical capacitors based on nitrogen-enriched cobalt (II) phthalocyanine/multi-walled carbon nanotube nanocomposites

    CSIR Research Space (South Africa)

    Lekitima, JN

    2013-11-01

    Full Text Available Based on Nitrogen-Enriched Cobalt (II) Phthalocyanine/Multi-walled Carbon Nanotube Nanocomposites Joel N. Lekitimaa, Kenneth I. Ozoemenaa,b,*, and Nagao Kobayashic a Department of Chemistry, University of Pretoria, Pretoria 0002, South Africa... non faradaic processes (double layer capacitance) and/or non faradaic processes (pseudo-capacitance). Various carbon materials such as carbon nanotubes CNTs) and activated carbons (ACs), because of their high surface area have been widely used...

  3. OPTICAL LIMITING EFFECT IN TWO PHTHALOCYANINES OBSERVED BY PICOSECOND PULSED LASER

    Institute of Scientific and Technical Information of China (English)

    QU SHI-LIANG; CHEN YU; SONG YING-LIN; CHEN GUO-PING; WANG YU-XIAO; ZHANG XUE-RU; LIU SHU-TIAN; WANG DUO-YUAN

    2001-01-01

    Optical limiting (OL) properties of two phthalocyanines were investigated by using picosecond laser pulses at 532nm. The relative ratios k of the absorption cross section of the first singlet excited state to that of the ground state were approximately obtained by the analysis of the experimental results in which the reverse saturable absorption model of the three-energy-level scheme was employed. A significant comparison with fullerene C60 was presented for OL. The OL mechanisms have been analysed in detail.

  4. Effect of New Water-Soluble Dendritic Phthalocyanines on Human Colorectal and Liver Cancer Cell Lines

    Directory of Open Access Journals (Sweden)

    Ebru YABAŞ

    2017-08-01

    Full Text Available Human hepatocellular carcinoma (HepG2 cells and colorectal adenocarcinoma (DLD-1 cells were treated with the synthesized water soluble phthalocyanine derivatives to understand the effect of the compounds both on colorectal and liver cancer cells. The compounds inhibited cell proliferation and displayed cytotoxic effect on these cancer cell lines however; the effect of the compounds on healthy control fibroblast cell line was comparatively lower. The compounds can be employed for cancer treatment as anticancer agents.

  5. Annealing assisted structural and surface morphological changes in Langmuir–Blodgett films of nickel octabutoxy phthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Shilpa Harish, T.; Viswanath, P., E-mail: viswanath@cnsms.res.in

    2016-01-01

    We report our studies on thin films of metallo-phthalocyanine (MPc), Nickel(II)1,4,8,11,15,18,22,25-octabutoxy-29H,31H-phthalocyanine (NiPc(OBu){sub 8}) transferred in a well defined thermodynamic state over a self assembled monolayer (octadecyl trichlorosilane)/SiO{sub 2}/Si substrate using the Langmuir–Blodgett (LB) method. The films are characterized using differential scanning calorimetry (DSC), grazing incidence X-ray diffraction (GIXD) and atomic force microscopy (AFM) techniques. DSC studies on powdered samples in the bulk indicate enantiotropic solid–solid phase transition. GIXD studies on the as-deposited LB film show a Bragg peak indicating crystallinity of the thin film. Annealing (373 K) results in reduction of lattice spacing (1.21 Å) signifying changes in molecular packing within the unit cell. At this stage, an additional Bragg peak is observed which grows at the expense of the former one and they coexist between 373 K and 423 K. A discontinuity in lattice spacing from 20.73 to 15.12 Å with annealing indicates clearly a structural change of the underlying crystalline lattice. Correspondingly, the surface morphology images obtained using AFM show, with annealing, a transformation from spherical granular morphology to elongated, flat crystallites suggesting asymmetric growth process. Statistical parameters of the grain extracted from the AFM images show that the size, fractal dimension and circularity are affected by annealing. Based on these studies, we infer the structural and surface morphological changes of the meta-stable phase (Form I) to the stable phase (Form II) in annealed LB films of phthalocyanine. - Highlights: • Langmuir–Blodgett (LB) films of phthalocyanine subjected to thermal annealing. • Structural transformation and coexistence of polymorphs in LB films • Surface morphology changes from nanoscale grains to elongated crystallites. • Reduction of fractal dimension and circularity index reveals asymmetric growth.

  6. Phthalocyanine adsorption to graphene on Ir(111): Evidence for decoupling from vibrational spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Endlich, M., E-mail: michael.endlich@tu-ilmenau.de; Gozdzik, S.; Néel, N.; Kröger, J., E-mail: joerg.kroeger@tu-ilmenau.de [Institut für Physik, Technische Universität Ilmenau, D-98693 Ilmenau (Germany); Rosa, A. L. da [Bremen Center for Computational Materials Science, University Bremen, D-28359 Bremen (Germany); Department of Physics, Federal University of Minas Gerais, 31270-901 Belo Horizonte, MG (Brazil); Frauenheim, T. [Bremen Center for Computational Materials Science, University Bremen, D-28359 Bremen (Germany); Wehling, T. O. [Bremen Center for Computational Materials Science, University Bremen, D-28359 Bremen (Germany); Institute for Theoretical Physics, University Bremen, D-28359 Bremen (Germany)

    2014-11-14

    Phthalocyanine molecules have been adsorbed to Ir(111) and to graphene on Ir(111). From a comparison of scanning tunneling microscopy images of individual molecules adsorbed to the different surfaces alone it is difficult to discern potential differences in the molecular adsorption geometry. In contrast, vibrational spectroscopy using inelastic electron scattering unequivocally hints at strong molecule deformations on Ir(111) and at a planar adsorption geometry on graphene. The spectroscopic evidence for the different adsorption configurations is supported by density functional calculations.

  7. Preparation of Organic Zn-Phthalocyanine-Based Semiconducting Materials and Their Optical and Electrochemical Characterization

    OpenAIRE

    Amira Hajri; Sarra Touaiti; Bassem Jamoussi

    2013-01-01

    In order to increase the species of organic semiconductors, new Zn-phthalocyanines-based organic materials were synthesized and characterized. The new compounds have been characterized by 1H and 13C using NMR, FTIR, and UV-Vis. The absorption, fluorescence, and electrochemical properties were also studied. Green photoluminescence was observed in dilute solutions. In solid thin films, π-π* interactions influenced the optical properties, and redshifted photoluminescence spectra were obtained; r...

  8. Biological decolorization of reactive anthraquinone and phthalocyanine dyes under various oxidation-reduction conditions.

    Science.gov (United States)

    Lee, Young H; Matthews, Rosalyn D; Pavlostathis, Spyros G

    2006-02-01

    The decolorization of two anthraquinone dyes (Reactive Blue 4 [RB4] and Reactive Blue 19 [RB19]) and two phthalocyanine dyes (Reactive Blue 7 [RB7] and Reactive Blue 21 [RB21]) was investigated at an initial dye concentration of 300 mg/L using an unacclimated, enrichment culture. The culture was fed a mixture of organic compounds and maintained initially under aerobic conditions, and then progressively developed anoxic/ anaerobic conditions. Biotransformation-related decolorization of the dyes did not take place under aerobic conditions, but use of the feed organic mixture and biomass production by the enrichment culture were not affected. Complete ammonia removal occurred in the control and all dye-amended cultures. The development and extent of nitrification were much lower in the latter cultures, in which ammonia removal via air stripping was the dominant mechanism. Prolonged incubation of the culture under anoxic/anaerobic conditions with multiple carbon source additions resulted in a high decolorization extent of anthraquinone dyes (over 84%) and only partial decolorization of phthalocyanine dyes (49 to 66%). Development of significant methanogenic activity took place in the control and, to a lesser extent, in the two phthalocyanine dye-amended cultures, but the anthraquinone dyes severely inhibited the development of methanogenic activity. The RB4 and RB19 decolorization was attributed to nonreversible, microbially mediated dye transformation(s), demonstrated by the accumulation of decolorization products with absorbance maxima in the 420- to 460-nm region. The decolorization of RB4 and RB19 followed Michaelis-Menten kinetics. At an initial dye concentration of 300 mg/L, the observed maximum decolorization rate per unit biomass was 9.1 and 37.5 mg dye/mg volatile suspended solids x day for the RB4 and RB19, respectively. Thus, partial decolorization of reactive phthalocyanine dyes and extensive biological decolorization of reactive anthraquinone dyes is

  9. Synthesis and Properties of Triazol-5-one Substituted Phthalocyanines by Microwave Irradiation

    OpenAIRE

    KAHVECİ, Bahittin; ŞAŞMAZ, Selami; ÖZİL, Musa; KANTAR, Cihan

    2006-01-01

    Triazol-5-one substituted phthalocyanines were prepared quickly by the reaction of 4-nitrophthalonitrile with anhydrous metal salts in DBU (1,8-diazabicyclo[5,4,0]undec-7-ene) and DMAE (dimethylaminoethanol) by microwave irradiation. Microwave yields were higher than those of the conventional synthesis methods. All of these complexes are insoluble in polar solvents such as ethanol, ethyl acetate and chloroform. The characterization of the compounds was accomplished by elemental anal...

  10. Effects of iron phthalocyanine on the inner pressure of MH/Ni battery

    Institute of Scientific and Technical Information of China (English)

    WANG Fang; WU Feng

    2004-01-01

    Effects of iron phthalocyanine (FePc) on the inner pressure of MH/Ni batteries during charging were examined. Experimental results show that the battery with appropriate quantity of FePc displays a much lower inner pressure under charging and overcharging than the battery without FePc, especially the battery with 1 mg FePc exhibits the slowest increasing speed of inner pressure and the best charging efficiency and overchargeability.

  11. Canine models of copper toxicosis for understanding mammalian copper metabolism

    OpenAIRE

    Fieten, Hille; Leegwater, Peter A. J.; Watson, Adrian L.; Rothuizen, Jan

    2011-01-01

    Hereditary forms of copper toxicosis exist in man and dogs. In man, Wilson’s disease is the best studied disorder of copper overload, resulting from mutations in the gene coding for the copper transporter ATP7B. Forms of copper toxicosis for which no causal gene is known yet are recognized as well, often in young children. Although advances have been made in unraveling the genetic background of disorders of copper metabolism in man, many questions regarding disease mechanisms and copper homeo...

  12. Phthalocyanine/chitosan-TiO{sub 2} photocatalysts: Characterization and photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Hamdi, A. [University of Sfax-Faculty of Science-LCI-Sfax-Tunisia (Tunisia); Boufi, S. [University of Sfax-Faculty of Science-LMSE-Sfax-Tunisia (Tunisia); Bouattour, S., E-mail: soraa.boufi@yahoo.com [University of Sfax-Faculty of Science-LCI-Sfax-Tunisia (Tunisia)

    2015-06-01

    Graphical abstract: - Highlights: • Hybrid chitosan–phthalocyanine-TiO{sub 2} photocatalyst are elaborated at room temperature without any calcination treatment. • After immersion in water, the alkoxide groups underwent hydrolysis and the (TiO{sub 6}) octahedra started to join together. • The enhanced activity of the hybrid catalyst is attributed to the cooperative role of the three components of the photocatalyst. - Abstract: Chitosan (CS) was used as a template to prepare a hybrid chitosan–phthalocyanine-TiO{sub 2} (PC/CS-TiO{sub 2}) photocatalyst at room temperature without any calcination treatment. The as-prepared hybrid photocatalyst (PC/CS-TiO{sub 2}) was characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and UV–vis diffuse reflectance spectroscopy (DRS). The results of the photodegradation of aniline, used as a model pollutant, revealed that the hybrid photocatalyst (PC/CS-TiO{sub 2}) exhibited a photocatalytic activity under visible-light irradiation. The enhanced activity of the hybrid catalyst is attributed to the cooperative role of the three components of the photocatalyst; chitosan as a template for the immobilization crystalline TiO{sub 2} nanoparticles, phthalocyanine that promote the light absorption in the visible range and TiO{sub 2} acting as an acceptor of electrons generated by the photons absorption to produce superoxide radicals.

  13. In situ metalation of free base phthalocyanine covalently bonded to silicon surfaces

    Science.gov (United States)

    Lupo, Fabio; Tudisco, Cristina; Bertani, Federico; Dalcanale, Enrico

    2014-01-01

    Summary Free 4-undecenoxyphthalocyanine molecules were covalently bonded to Si(100) and porous silicon through thermic hydrosilylation of the terminal double bonds of the undecenyl chains. The success of the anchoring strategy on both surfaces was demonstrated by the combination of X-ray photoelectron spectroscopy with control experiments performed adopting the commercially available 2,3,9,10,16,17,23,24-octakis(octyloxy)-29H,31H-phthalocyanine, which is not suited for silicon anchoring. Moreover, the study of the shape of the XPS N 1s band gave relevant information on the interactions occurring between the anchored molecules and the substrates. The spectra suggest that the phthalocyanine ring interacts significantly with the flat Si surface, whilst ring–surface interactions are less relevant on porous Si. The surface-bonded molecules were then metalated in situ with Co by using wet chemistry. The efficiency of the metalation process was evaluated by XPS measurements and, in particular, on porous silicon, the complexation of cobalt was confirmed by the disappearance in the FTIR spectra of the band at 3290 cm−1 due to –NH stretches. Finally, XPS results revealed that the different surface–phthalocyanine interactions observed for flat and porous substrates affect the efficiency of the in situ metalation process. PMID:25551050

  14. In situ metalation of free base phthalocyanine covalently bonded to silicon surfaces

    Directory of Open Access Journals (Sweden)

    Fabio Lupo

    2014-11-01

    Full Text Available Free 4-undecenoxyphthalocyanine molecules were covalently bonded to Si(100 and porous silicon through thermic hydrosilylation of the terminal double bonds of the undecenyl chains. The success of the anchoring strategy on both surfaces was demonstrated by the combination of X-ray photoelectron spectroscopy with control experiments performed adopting the commercially available 2,3,9,10,16,17,23,24-octakis(octyloxy-29H,31H-phthalocyanine, which is not suited for silicon anchoring. Moreover, the study of the shape of the XPS N 1s band gave relevant information on the interactions occurring between the anchored molecules and the substrates. The spectra suggest that the phthalocyanine ring interacts significantly with the flat Si surface, whilst ring–surface interactions are less relevant on porous Si. The surface-bonded molecules were then metalated in situ with Co by using wet chemistry. The efficiency of the metalation process was evaluated by XPS measurements and, in particular, on porous silicon, the complexation of cobalt was confirmed by the disappearance in the FTIR spectra of the band at 3290 cm−1 due to –NH stretches. Finally, XPS results revealed that the different surface–phthalocyanine interactions observed for flat and porous substrates affect the efficiency of the in situ metalation process.

  15. Time-resolved spectroscopic studies of sulphonated aluminium phthalocyanine triplet states

    Science.gov (United States)

    Simpson, Mary S. C.; Beeby, A.; Bishop, Steven M.; MacRobert, Alexander J.; Parker, Andrew W.; Phillips, David

    1992-04-01

    The photophysical and photochemical properties of sulphonated aluminum and zinc phthalocyanines have been investigated in a range of solvents and model biological systems. Anomalous effects are observed upon deuteration of the solvent and addition of fluoride ions. In D2O the excited singlet and triplet state lifetimes and quantum yields of fluorescence and triplet state formation are increased relative to H2O. No solvent isotope effect is observed between CH3OH and CH3OD. It is proposed that relaxation of the excited state involves a tunnelling type interaction in which the phthalocyanine's highly energetic metal-axial ligand stretching vibrations are coupled to the HO-H or DO-D stretching vibrations. A significant increase in triplet lifetimes of phthalocyanine sensitizers bound to protein substrates is observed which is a function of the degree of sulphonation. The implications of these results to the determination of the quantum yields of singlet oxygen formation in D2O and lipophilic environments are discussed.

  16. Analysis of photoluminescence decay kinetics of aluminum phthalocyanine nanoparticles interacting with immune cells

    Directory of Open Access Journals (Sweden)

    F. G. Bystrov

    2016-01-01

    Full Text Available This work is dedicated to the study of the photoluminescence kinetics of aluminum phthalocyanine nanoparticles in colloidal solutions at different pH and in the interaction with immune cells (macrophages. For measurements we used a registration system based on Hamamatsu streak camera (C10627-13 Hamamatsu Photonics with picosecond temporal resolution (15 ps, conjugated with the fiberoptic spectrometer and picosecond laser pumping. The changes in fluorescence decay kinetics as additional lifetime components of fluorescence were found during the experiment. The number of components and duration of lifetimes changed while interacting with cells and depends on pH. At pH 2 the presence of two fluorescence lifetimes was recorded: the first one was 5 ns, which corresponded to the molecular form in solution, and 1.5 ns, which corresponded to bound state of phthalocyanine molecules. Due to the absence of other possible objects for bounding in the solution except of the nanoparticles we can suggest with a high degree of accuracy that the bounding occurs with the very these nanoparticles. Analysis of the fluorescence lifetimes of aluminum phthalocyanine nanoparticles in macrophages indicated the presence of two components: 9 ns and 4.5 ns. A model of surface molecules transitions from parallel to perpendicular position, regarding to the plane of the crystal nanoparticle was proposed.

  17. Conjugates of Phthalocyanines With Oligonucleotides as Reagents for Sensitized or Catalytic DNA Modification

    Directory of Open Access Journals (Sweden)

    2006-01-01

    Full Text Available Several conjugates of metallophthalocyanines with deoxyribooligonucleotides were synthesized to investigate sequence-specific modification of DNA by them. Oligonucleotide parts of these conjugates were responsible for the recognition of selected complementary sequences on the DNA target. Metallophthalocyanines were able to induce the DNA modification: phthalocyanines of Zn(II and Al(III were active as photosensitizers in the generation of singlet oxygen 1 O 2 , while phthalocyanine of Co(II promoted DNA oxidation by molecular oxygen through the catalysis of formation of reactive oxygen species ( ⋅ O 2 − , O 2 H 2 , OH. Irradiation of the reaction mixture containing either Zn(II- or Al(III-tetracarboxyphthalocyanine conjugates of oligonucleotide pd(TCTTCCCA with light of > 340 nm wavelength (Hg lamp or He/Ne laser resulted in the modification of the 22-nucleotide target d(TGAATGGGAAGAGGGTCAGGTT. A conjugate of Co(II-tetracarboxyphthalocyanine with the oligonucleotide was found to modify the DNA target in the presence of O 2 and 2-mercaptoethanol or in the presence of O 2 H 2 . Under both sensitized and catalyzed conditions, the nucleotides G 13 – G 15 were mainly modified, providing evidence that the reaction proceeded in the double-stranded oligonucleotide. These results suggest the possible use of phthalocyanine-oligonucleotide conjugates as novel artificial regulators of gene expression and therapeutic agents for treatment of cancer.

  18. Electrocatalytic amperometric determination of amitrole using a cobalt-phthalocyanine-modified carbon paste electrode.

    Science.gov (United States)

    Chicharro, Manuel; Zapardiel, Antonio; Bermejo, Esperanza; Moreno, Mónica; Madrid, Elena

    2002-07-01

    Cobalt-phthalocyanine-modified carbon paste electrodes are shown to be excellent indicators for electrocatalytic amperometric measurements of triazolic herbicides such as amitrole, at low oxidation potentials (+0.40 V). The detection and determination of amitrole in flow injection analysis with a modified carbon paste electrode with Co-phthalocyanine is described. The concentrations of amitrole in 0.1 M NaOH solutions were determined using the electrocatalytic oxidation signal corresponding to the Co(II)/Co(III) redox process. A detection limit of 0.04 microg mL(-1) (4 ng amitrole) was obtained for a sample loop of 100 microL at a fixed potential of +0.55 V (vs. Ag/AgCl) in 0.1 M NaOH and a flow rate of 4.0 mL min(-1). Furthermore, the modified carbon paste electrodes offers reproducible responses in such a system, and the relative standard deviation was 3.3% using the same surface, 5.1% using different surface, and 6.9% using different pastes. The performance of the cobalt-phthalocyanine-modified carbon paste electrodes is illustrated here for the determination of amitrole in commercial formulations. The response of the electrodes is stable, with more than 80% of the initial retained activity after 50 min of continuous use.

  19. Hair copper in intrauterine copper device users.

    Science.gov (United States)

    Thiery, M; Heyndrickx, A; Uyttersprot, C

    1984-03-01

    The antifertility effect of copper-bearing IUDs is based on continuous release of copper, which is a result of the reaction between the metal and the uterine secretions. Released cupric ions collect in the endometrium and in the uterine fluid but significant accumulation has not been found in the bloodstream or elsewhere. Following Laker's suggestion that hair be used for monitoring essential trace elements, e.g., copper, we checked the copper content of the hair of women wearing copper-bearing IUDs. Samples of untreated pubic hair removed by clipping before diagnostic curettage were obtained from 10 young (24-34 years old), white caucasian females who until then had been wearing an MLCu250 IUD for more than 1 year. Pubes from 10 comparable (sex, age, race) subjects who had never used a Cu-containing device served as controls. The unwashed material was submitted to the toxicology laboratory, where the copper content was assessed by flameless atomic absorption, a technique whose lower limit of measurement lies at a concentration of 0.05 mcg Cu/ml fluid (50 ppb). Hair samples were washed to remove extraneous traces of metal according to the prescriptions of the International Atomic Energy Agency, weighed, and mineralized, after which a small volume (10 mcl) of the diluted fluid was fed into the graphite furnace. Each sample (75-150 mg) was analyzed 4 times, both before and after washing. Since the cleaning procedure reduces the weight of the sample (mainly by the removal of fat, dust, etc.) this explains why the percentage copper content of washed hair is higher than that of unwashed hair belonging to the same subject. The results indicate that there was no significant difference (Mann-Whitney U test) between the mean copper levels of both unwashed and washed pubes from women who were using or had never used an MLCu250 IUD. We therefore conclude that the use of this copper-containing device is not associated with significant accumulation of copper in (pubic) hair.

  20. China Copper Processing Industry Focus

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    <正>1. Market Consumption The ’China Factor’ and Copper Price Fluctuation We all know China is an enormous consumer of copper,but the exact levels of consumption and where the copper has gone remains a mystery.

  1. Biogenic nanoparticles: copper, copper oxides, copper sulphides, complex copper nanostructures and their applications.

    Science.gov (United States)

    Rubilar, Olga; Rai, Mahendra; Tortella, Gonzalo; Diez, Maria Cristina; Seabra, Amedea B; Durán, Nelson

    2013-09-01

    Copper nanoparticles have been the focus of intensive study due to their potential applications in diverse fields including biomedicine, electronics, and optics. Copper-based nanostructured materials have been used in conductive films, lubrification, nanofluids, catalysis, and also as potent antimicrobial agent. The biogenic synthesis of metallic nanostructured nanoparticles is considered to be a green and eco-friendly technology since neither harmful chemicals nor high temperatures are involved in the process. The present review discusses the synthesis of copper nanostructured nanoparticles by bacteria, fungi, and plant extracts, showing that biogenic synthesis is an economically feasible, simple and non-polluting process. Applications for biogenic copper nanoparticles are also discussed.

  2. Impact of the Anchoring Ligand on Electron Injection and Recombination Dynamics at the Interface of Novel Asymmetric Push-Pull Zinc Phthalocyanines and TiO2

    NARCIS (Netherlands)

    Sharma, Divya; Steen, Gerrit Willem; Korterik, Jeroen P.; Garcia-Iglesias, M.; Vazquez, P; Torres, T.; Herek, Jennifer Lynn; Huijser, Jannetje Maria

    2013-01-01

    Phthalocyanines are promising photosensitizers for dye-sensitized solar cells (DSSCs). A parameter that has been problematic for a long time involves electron injection (EI) into the TiO2. The development of push-pull phthalocyanines shows great potential to improve the ratio of EI to back electron

  3. Impact of the Anchoring Ligand on Electron Injection and Recombination Dynamics at the Interface of Novel Asymmetric Push-Pull Zinc Phthalocyanines and TiO2

    NARCIS (Netherlands)

    Sharma, D.; Steen, G.W.; Korterik, J.P.; Garcia-Iglesias, M.; Vazquez, P; Torres, T.; Herek, J.L.; Huijser, J.M.

    2013-01-01

    Phthalocyanines are promising photosensitizers for dye-sensitized solar cells (DSSCs). A parameter that has been problematic for a long time involves electron injection (EI) into the TiO2. The development of push-pull phthalocyanines shows great potential to improve the ratio of EI to back electron

  4. Synthesis of single-walled carbon nanotubes by the pyrolysis of a compression activated iron(II) phthalocyanine/phthalocyanine metal-free derivative/ferric acetate mixture

    Indian Academy of Sciences (India)

    Tawanda Mugadza; Edith Antunes; Tebello Nyokong

    2015-07-01

    This paper reports on the synthesis of single walled carbon nanotubes (SWCNTs) from an activated mixture of iron (II) phthalocyanine, its metal-free derivative and ferric acetate. The powdered mixture was activated by compression into a tablet by applying a force of 300 kN, followed by re-grinding into powder and heating it to high temperatures (1000°C). The activation by compression resulted in more than 50% debundling of SWCNTs as judged by transition electron microscopy. Acid functionalization of the SWCNTs was confirmed by the increase in the D:G ratio from 0.56 to 0.87 in the Raman spectra and the observation of an average of one carboxylic acid group per 13 carbon atoms from thermogravimetric analysis (TGA). TGA also showed that the initial decomposition temperatures for the activated and non-activated mixtures to be 205°C and 245°C, respectively. Hence, activation leads to the lowering of the pyrolysis temperature of the phthalocyanines. X-ray diffraction, electronic absorption and Fourier transform infrared spectra were also employed to characterize the SWCNT.

  5. Saccharide Substituted Zinc Phthalocyanines: Optical Properties, Interaction with Bovine Serum Albumin and Near Infrared Fluorescence Imaging for Sentinel Lymph Nodes

    Directory of Open Access Journals (Sweden)

    Li Lu

    2014-01-01

    Full Text Available Saccharide-substituted zinc phthalocyanines, [2,9(10,16(17,23(24-tetrakis((1-(β-D-glucose-2-yl-1H-1,2,3-triazol-4-ylmethoxyphthalocyaninato]zinc(II and [2,9(10, 16(17,23(24-tetrakis((1-(β-D-lactose-2-yl-1H-1,2,3-triazol-4-ylmethoxyphthalocyaninato] zinc(II, were evaluated as novel near infrared fluorescence agents. Their interaction with bovine serum albumin was investigated by fluorescence and circular dichroism spectroscopy and isothermal titration calorimetry. Near infrared imaging for sentinel lymph nodes in vivo was performed using nude mice as models. Results show that saccharide- substituted zinc phthalocyanines have favourable water solubility, good optical stability and high emission ability in the near infrared region. The interaction of lactose-substituted phthalocyanine with bovine serum albumin displays obvious differences to that of glucose- substituted phthalocyanine. Moreover, lactose-substituted phthalocyanine possesses obvious imaging effects for sentinel lymph nodes in vivo.

  6. Synthesis and characterization of near-IR absorbing metal-free and zinc(II phthalocyanines modified with aromatic azo groups

    Directory of Open Access Journals (Sweden)

    Mukaddes Özçeşmeci

    2015-05-01

    Full Text Available Metal-free and zinc(II phthalocyanine complexes bearing peripheral (E-4-((2-hydroxynaphthalen-1-yldiazenyl units have been synthesized. Novel phthalonitrile derivative required for the preparation of phthalocyanine complexes was prepared by coupling 4-aminophthalonitrile and 2-naphthol. The structures of these new compounds were characterized by using elemental analyses, proton nuclear magnetic resonance, fourier transform infrared spectroscopy, ultraviolet–visible spectroscopy, fluorescence spectroscopy and mass spectrometry. In the UV-Vis spectra a broad absorption band appears for phthalocyanine complexes at around 450–500 nm resulting from azo-group introduced onto the phthalocyanine ring. The photophysical properties of metal-free and zinc(II phthalocyanines were studied in tetrahydrofuran.

  7. Photophysical and redox properties of a series of phthalocyanines: relation with their photodynamic activities on TF-1 and Daudi leukemic cells.

    Science.gov (United States)

    Daziano, J P; Steenken, S; Chabannon, C; Mannoni, P; Chanon, M; Julliard, M

    1996-10-01

    The photodynamic therapy (PDT) efficiency of five phthalocyanines, chloroaluminum phthalocyanine (AlPc), dichlorosilicon phthalocyanine (SiPc), bis(tri-n-hexylsiloxy)silicon phthalocyanine (PcHEX), bis(triphenylsiloxy)silicon phthalocyanine (PcPHE) and nickel phthalocyanine (NiPc), was assessed on two leukemic cell lines TF-1 and erythroleukemic and B lymphoblastic cell lines, Daudi, respectively. AlPc showed the best photocytotoxicity leading to 0.008 surviving fraction at 2 x 10(-9) M for TF-1 and 4 x 10(-9) M for Daudi. A1 5 x 10(-7) M, SiPc and PcHEX induced a significant photokilling, whereas NiPc and PcPHE were inactive. Laser flash photolysis and photoredox properties of the phthalocyanines were investigated to try to relate these parameters with the biological effects. AlPc showed the longest triplet life-time: 484 microseconds in dimethyl sulfoxide/H2O. This value was increased up to 820 microseconds when AlPc was complexed with human serum albumin used as a membrane model. Such an enhancement was not observed with the silicon phthalocyanines. Upon irradiation, all the phthalocyanines generated singlet oxygen with 0.29-0.37 quantum yield values. The reduction potentials of the excited states obtained from measurement in the ground state and energy of the excited triplets show that AlPc is the best electron acceptor. The in vitro photocytotoxicity observed and the measured parameters are in agreement with a key role of electron transfer in PDT assays involving these phthalocyanines.

  8. Copper and silver halates

    CERN Document Server

    Woolley, EM; Salomon, M

    2013-01-01

    Copper and Silver Halates is the third in a series of four volumes on inorganic metal halates. This volume presents critical evaluations and compilations for halate solubilities of the Group II metals. The solubility data included in this volume are those for the five compounds, copper chlorate and iodate, and silver chlorate, bromate and iodate.

  9. Coping with copper

    DEFF Research Database (Denmark)

    Nunes, Ines; Jacquiod, Samuel; Brejnrod, Asker

    2016-01-01

    Copper has been intensively used in industry and agriculture since mid-18(th) century and is currently accumulating in soils. We investigated the diversity of potential active bacteria by 16S rRNA gene transcript amplicon sequencing in a temperate grassland soil subjected to century-long exposure......, suggesting a potential promising role as bioindicators of copper contamination in soils....

  10. Photoelectrochemical Character of TiO2 Nanocrystalline Electrodes Sensitized by Aluminum Phthalocyanines Modified with Sulfonate Groups

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Particular kinds of TiO2 nanocrystalline electrodes were sensitized by aluminum phthalocyanines modified with sulfonate groups [Al(OH)PcSn]. It was found that in the red region, the electrodes show obvious photoelectrical responses. The surface photovoltage spectra and photocurrent action spectra indicate that in the red region, the monomers of aluminum phthalocyanines have a greater influence on the determination of the photoelectrical response of TiO2 electrodes than the dimers. The dye-sensitized solar cells were obtained by using the aluminum phthalocyanines-sensitized TiO2 electrodes and Pt electrodes, which have an open circuit photovoltage of 360 mV, a short circuit photocurrent of 39.4 μA/cm2, a fill factor of 0.54 and a maximum power output of 7.65 μW/cm2 under a light intensity of 50 mW/cm2.

  11. Investigation of the aluminum phthalocyanine nanoparticles colloidal solutions pH-dependent photoluminescence kinetics in pico- and nanosecond time range

    Science.gov (United States)

    Bystrov, F. G.; Makarov, V. I.; Loschenov, V. B.

    2016-08-01

    In this study, the fluorescence intensity decay of aluminum phthalocyanine nanoparticles colloidal solutions at different pH was investigated. Hamamatsu Streak-Camera (C10627 - 13 Hamamatsu Photonics) with picosecond temporal resolution (15 ps) was used to carry out the measurements. For excitation we used Hamamatsu Picosecond Light Pulser PLP - 10 with 637 nm wavelength and 65 ps pulse duration. The changes in fluorescence decay kinetics were found during the experiment. The number of fluorescence lifetime components and duration of lifetimes depends on pH. At pH 2 the presence of two fluorescence lifetimes was recorded: the first one was 5 ns, which corresponded to the molecular form in solution, and 1.5 ns, which corresponded to bound state of phthalocyanine molecules. This work is a preparatory step towards a model which describes the interaction of aluminum phthalocyanine nanoparticles with environment in biological tissue.

  12. A density functional theory investigation of charge mobility in titanyl-phthalocyanines and their tailored peripherally substituted complexes

    CERN Document Server

    De Lile, Jeffrey R

    2016-01-01

    Titanyl-phthalocyanines catalytic ability towards oxygen reduction is demonstrated in experimental literature. Our recent theoretical simulations revealed electronic structure origin of catalytic ability in peripherally and axially substituted triplet and singlet titanyl-phthalocyanines. However, the origin of high electron transfer ability to spontaneously reduce peroxide in chlorine substituted singlet complex and triplet state Ti(II)Pc complexes remain elusive. Thus, we performed density functional theory calculations to study Ti(IV)Pc and their tailored peripheral substituted complexes as representative compounds of titanyl-phthalocyanines for charge mobilities, reorganization energies and electronic couplings. In addition, oxo(phthalocyaninato)titanium(IV) (TiOPc) convex and concave compounds were investigated to benchmark the method. Based on the results, Reorganization energies of triplet state Ti(II)Pc and their tailored peripheral substituted complexes are compared with Ti(IV)Pc singlet complexes in ...

  13. Microwave-assisted synthesis, characterization and spectral properties of non-peripherally tetra-substituted phthalocyanines containing eugenol moieties

    Science.gov (United States)

    Kantar, Cihan; Şahin, Zarife Sibel; Büyükgüngör, Orhan; Şaşmaz, Selami

    2015-06-01

    The microwave-assisted synthesis and characterization of novel non-peripherally eugenol substituted metallophthalocyanines (M: Co(II), Ni(II), Cu(II), Zn(II)) have been reported for the first time in this study. All the new compounds were characterized by a combination of FT-IR, 1H NMR, 13C NMR, and UV/vis spectroscopy techniques. The crystal structure of compound (1) was also determined by the single crystal diffraction technique. Newly synthesized eugenol substituted phthalocyanines have more redshift Q bands (about 17-18 nm) than previously reported eugenol substituted phthalocyanines. Zinc(II)phthalocyanine (1d) has an extra absorption band at 746 nm that calling "X band" at UV/vis spectrum.

  14. Model of In Situ Composite of Cobalt(Ⅱ)-Phthalocyanine and Carbonyl Iron for Organic/Inorganic Nanocomposites

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Cobalt-phthalocyanine/iron nanocomposite particles have been obtained using method of composite in situ,with the mixture of carbonyl iron and solution of cobalt(Ⅱ)-phthalocyanine (Co-Pc) ultrasonic dispersing in N,N-dimethyl-formamide (DMF).Structure characterization of their inner and surface have relation with method of carbonyl iron joined in the mixture,contents of carbonyl iron and Co-Pc in the mixture of Co-Pc ultrasonic dispersing in DMF.With a method of composite in situ controlling reasonable experiment condition,it can be obtained that cobalt-phthalocyanine/iron nanocomposite particles has completely been covered with Co-Pc,they had structure of Chinese gooseberry in inner and mere made up of almost regular spherical shape and the average diameter is 1.4 μm.

  15. Kunpeng Copper:The largest Copper Smelting Company of Sichuan

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    <正>On September 9,Liangshan Mining Company’s 100,000 tons/year cathode copper project kicked off.It is another key project of the company following the successful launch of the 100,000 tons/year anode copper project.Based on ISA copper smelting technology of the largest open-cast copper mine in southwest China,

  16. Preparation and Characterization of Cu and Ni on Alumina Supports and Their Use in the Synthesis of Low-Temperature Metal-Phthalocyanine Using a Parallel-Plate Reactor

    Directory of Open Access Journals (Sweden)

    Carlos J. Lucio-Ortiz

    2013-09-01

    Full Text Available Ni- and Cu/alumina powders were prepared and characterized by X-ray diffraction (XRD, scanning electronic microscope (SEM, and N2 physisorption isotherms were also determined. The Ni/Al2O3 sample reveled agglomerated (1 μm of nanoparticles of Ni (30–80 nm however, NiO particles were also identified, probably for the low temperature during the H2 reduction treatment (350 °C, the Cu/Al2O3 sample presented agglomerates (1–1.5 μm of nanoparticles (70–150 nm, but only of pure copper. Both surface morphologies were different, but resulted in mesoporous material, with a higher specificity for the Ni sample. The surfaces were used in a new proposal for producing copper and nickel phthalocyanines using a parallel-plate reactor. Phthalonitrile was used and metallic particles were deposited on alumina in ethanol solution with CH3ONa at low temperatures; ≤60 °C. The mass-transfer was evaluated in reaction testing with a recent three-resistance model. The kinetics were studied with a Langmuir-Hinshelwood model. The activation energy and Thiele modulus revealed a slow surface reaction. The nickel sample was the most active, influenced by the NiO morphology and phthalonitrile adsorption.

  17. Cu-酞菁配合物在MCM-41中的装载研究%The Study of Encapsulation of Metal-phthalocyanine in Mesoporous Molecular Sieves MCM-41

    Institute of Scientific and Technical Information of China (English)

    崔子祥; 薛永强; 杜锡光; 李萍

    2011-01-01

    The2(3), 9(10), 16(17), 23 (24)-tetra-(N, N-bisethylamineethoxyl) Cu(Ⅱ)-phthalocyanine complexes with flexible peripheral substituents were synthesized and encapsulated in mesoporous molecular sieves MCM-41. The prepared samples were characterized by UV-vis-Nir, FT-IR, XRD, TEM, FESEM and N2 adsorption-desoption isotherms. Results show that the prepared phothalocyanine copper ( Ⅱ ) was encapsulated in mesoporous molecular sieves MCM-41 in the form of monomer and dimer. The phothalocyanine copper ( II ) encapsulated in MCM-41 with high concentration was in favour of preparing mesoporous molecular sieves samples with higher crystallinity and pore channel order.%合成了具有柔性取代基的2(3),9(10),16(17),23(24)-四-(N,N-二-乙胺基乙氧基)Cu-酞菁配合物,并且装载到MCM-41中.利用UV-Vis-Nir,FT-IR,XRD,TEM,FESEM及N2吸附-脱附等温线对制备的样品进行了表征.研究表明:制备的Cu-酞菁配合物能够装载到MCM-41中;较高浓度的Cu-酞菁配合物在MCM-41中的装载,有利于制备结晶度及孔道有序性较高的介孔分子筛样品.

  18. Preparation and Characterization of Cu and Ni on Alumina Supports and Their Use in the Synthesis of Low-Temperature Metal-Phthalocyanine Using a Parallel-Plate Reactor.

    Science.gov (United States)

    Sánchez-De la Torre, Fernando; De la Rosa, Javier Rivera; Kharisov, Boris I; Lucio-Ortiz, Carlos J

    2013-09-30

    Ni- and Cu/alumina powders were prepared and characterized by X-ray diffraction (XRD), scanning electronic microscope (SEM), and N₂ physisorption isotherms were also determined. The Ni/Al₂O₃ sample reveled agglomerated (1 μm) of nanoparticles of Ni (30-80 nm) however, NiO particles were also identified, probably for the low temperature during the H2 reduction treatment (350 °C), the Cu/Al₂O₃ sample presented agglomerates (1-1.5 μm) of nanoparticles (70-150 nm), but only of pure copper. Both surface morphologies were different, but resulted in mesoporous material, with a higher specificity for the Ni sample. The surfaces were used in a new proposal for producing copper and nickel phthalocyanines using a parallel-plate reactor. Phthalonitrile was used and metallic particles were deposited on alumina in ethanol solution with CH₃ONa at low temperatures; ≤60 °C. The mass-transfer was evaluated in reaction testing with a recent three-resistance model. The kinetics were studied with a Langmuir-Hinshelwood model. The activation energy and Thiele modulus revealed a slow surface reaction. The nickel sample was the most active, influenced by the NiO morphology and phthalonitrile adsorption.

  19. Preparation and Dielectric Properties of a-MWNTs/Poly ( metal phthalocyanine) imide Copolymers%聚(金属酞菁)酰亚胺/碳纳米管复合材料的制备及介电性能

    Institute of Scientific and Technical Information of China (English)

    张丽梅; 王琦桐; 杨旭; 姜振华; 张云鹤

    2012-01-01

    以四氨基铜(锌)酞菁为四胺单体,与4,4'-二苯醚二胺(4,4'-ODA)和二苯醚四酸酐(ODPA)进行共聚,合成了聚(金属酞菁)酰亚胺.由于金属酞菁的引入,聚(铜酞菁)酰亚胺和聚(锌酞菁)酰亚胺的介电常数均高于传统聚酰亚胺(PI).以聚(铜酞菁)酰亚胺为基体,采用溶液共混的方法,制备了一系列碳纳米管/聚(铜酞菁)酰亚胺复合材料,碳纳米管较为均匀地分散在聚合物基体中.复合材料具有良好的介电性能,掺杂碳纳米管质量分数为20%的复合材料的介电常数达到200,介电损耗为2.25.%Poly (metal phthalocyanine) imide copolymers [P(MPc)I] were prepared with tetra-phthalocya-nine teraamines(4NH2-MPc) , 4,4'-diamino diphenyl ether(4,4'-ODA) , and 4,4'-oxydiphthalic anhydride (ODPA). The dielectric constants of the polymer are higher than traonditional polyimide(PI). Carbon nano-tubes/poly(copper phthalocyanine)imide [a-MWNTs/P(CuPc)I] composites with different contents of carbon nanotubes were prepared using solution method. Carbon nanotubes show good dispersion in P(CuPc)I matrix. The composite containing 20% carbon nanotubes have high dielectric constant of ca. 200 and low dielectric loss of ca. 2. 25(at 1 kHz) which show good dielectric properties.

  20. Towards the anti-fibrillogenic activity of phthalocyanines with out-of-plane ligands: correlation with self-association proneness

    Directory of Open Access Journals (Sweden)

    Kovalska V. B.

    2013-11-01

    Full Text Available Aim. The activity of five hafnium phthalocyanines containing out-of-plane ligands as inhibitors of reaction of insulin fibril formation is studied and correlation between their inhibitory properties and tendency to self-association is discussed. Methods. Fluorescence and absorption spectroscopy. Results. For the complexes with weak proneness to self-association PcHfDbm2, PcHfPyr2, and PcHfBtfa2 the values of inhibitory activity were estimated as 60–73 %. For phthalocyanines with the pronounced tendency to self-association PcHfPiromelit and PcHfCl2 the noticeably higher inhibitory activity values (about 95 % were shown. In the presence of native or fibrilar insulin the destruction of self-associates of metal complex occurs in buffer pH 7.9, Besides upon the conditions of insulin fibrillization reaction (0.1 M HCl phthalocyanines exist predominantly as monomers. Conclusions. The phthalocyanines with out-of-plane ligands with higher tendency to self-association have shown higher inhibitory activity in the insulin fibril formation comparing with the poorly aggregated metal complexes. At the same time low-order self-associates are not involved directly in the mechanism of inhibition of insulin fibrillization and the phthalocyanines bind with protein in monomeric form. Tendency of phthalocyanines to self-association in aqueous media seems to be an «indicator» of their proneness to stack with protein aromatic amino-acids and thus of anti-fibrilogenic properties.

  1. 轴向取代金属酞菁的制备及 Li/SOCl2电池催化性能研究%Preparation of Axially Substituted Metal Phthalocyanine and Catalytic Performance Study of Li/SOCl2 Battery

    Institute of Scientific and Technical Information of China (English)

    李莹莹; 赵建社

    2014-01-01

    Two series complexes of axially substituted metal phthalocyanines were synthesized by micro -wave and liquid phase method by using o-benzene diacetonitrile and metal salts as starting material , and the catalytic activity to lithium/thionyl chloride batteries were investigated .The results reveal that the ad-dition of catalyst can obviously increase the discharge voltage and time of Li /SOCl2 battery compared with the blank experiment , in which the relative energy of benzo Isoindoline axially substituted silicon phthalo-cyanine increased by 112 .62%, relative energy of copper phthalocyanine increased by 81.96%.%以邻苯二腈和金属盐为原料,分别采用微波法和液相法合成了两个系列13种轴向取代金属酞菁配合物,并对所合成的金属酞菁进行了锂/亚硫酰氯( Li/SOCl2)电池催化性能测试,结果表明:与空白实验相比较,催化剂的加入可以明显提高 Li/SOCl2电池的放电电压和放电时间。其中,铜酞菁放电电量提高81.96%,苯并异吲哚啉轴向取代硅酞菁放电量提高112.62%。

  2. Improved syntheses of high hole mobility phthalocyanines: A case of steric assistance in the cyclo-oligomerisation of phthalonitriles

    Directory of Open Access Journals (Sweden)

    Daniel J. Tate

    2012-01-01

    Full Text Available It has been shown that the base-initiated cyclo-oligomerisation of phthalonitriles is favoured by bulky α-substituents making it possible to obtain the metal-free phthalocyanine directly and in high yield. The phthalocyanine with eight α-isoheptyl substituents gives a high time-of-flight hole mobility of 0.14 cm2·V−1·s−1 within the temperature range of the columnar hexagonal phase, that is 169–189 °C.

  3. Novel planar binuclear zinc phthalocyanine sensitizer for dye-sensitized solar cells: Synthesis and spectral, electrochemical, and photovoltaic properties

    Science.gov (United States)

    Zhu, Baiqing; Zhang, Xuejun; Han, Mingliang; Deng, Pengfei; Li, Qiaoling

    2015-01-01

    A planar binuclear zinc phthalocyanine was newly synthesized for use in dye-sensitized solar cells, based on Schiff base and asymmetric amino zinc phthalocyanine. The novel compounds were characterized using FTIR, UV-Vis, 1H NMR, cyclic voltammetry and elemental analysis. From the reduction and oxidation behavior, it is proved that APC and bi-NPC have negative LUMO levels and positive HOMO levels, satisfying the energy gap rule, and can be employed as sensitizers for dye-sensitized solar cells (DSSCs) applications.

  4. Posttranslational regulation of copper transporters

    NARCIS (Netherlands)

    van den Berghe, P.V.E.

    2009-01-01

    The transition metal copper is an essential cofactor for many redox-active enzymes, but excessive copper can generate toxic reactive oxygen species. Copper homeostasis is maintained by highly conserved proteins, to balance copper uptake, distribution and export on the systemic and cellular level. Th

  5. Electrochemical Behavior and Characterization of Polypyrrole-Copper Phthalocyanine Tetrasulfonate Thin Film: Cyclic Voltammetry and in Situ Raman Spectroscopic Investigation

    Science.gov (United States)

    1990-01-10

    0.665 V diffused into the bulk of the solution instead of forming MVNO 3 film. These results indicated that the solubility of MVNO 3 was much higher...oxidation of PMV (or MVNO3 ). A much thinner PMV film (or MVNO 3) must be formed on the PPy-CuPcTs film during the reduction of 2+ to M in the NaNO3

  6. Hexagonal mesoporous silica modified with copper phthalocyanine as a photocatalyst for pesticide 2,4-dichlorophenoxiacetic acid degradation.

    Science.gov (United States)

    DeOliveira, Edimar; Neri, Cláudio R; Ribeiro, Anderson O; Garcia, Vinícius S; Costa, Leonardo L; Moura, Aline O; Prado, Alexandre G S; Serra, Osvaldo A; Iamamoto, Yassuko

    2008-07-01

    A new mesoporous catalyst was prepared by the reaction between 3-aminopropyltrimethoxisylane and Cu(II)-hexadecafluorophthalocyanine, followed by co-condensation of tetraethylorthosilicate around a micelle formed by n-dodecylamine. The surfactant was removed from the pores by continuous extraction with ethanol, giving the Si-CuF16Pc catalyst. This catalyst was characterized by SEM, FTIR, TGA, 29Si NMR, N2 adsorption and X-ray diffraction. SEM images confirmed that the catalyst material is formed by nanoaggregates with a diameter of 100 nm. N2 adsorption isotherms showed that Si-CuF16Pc has a surface area of approximately 200 m2 g(-1) and a porous diameter of 7.7 nm, characterizing the mesoporosity of this product. This novel material shows an excellent photocatalytic activity, degrading almost 90% of 2,4-dichlorophenoxyacetic acid (2,4-D) up to 30 min, while only approximately 40% of photodegradation was obtained in its absence.

  7. Fabricating Copper Nanotubes by Electrodeposition

    Science.gov (United States)

    Yang, E. H.; Ramsey, Christopher; Bae, Youngsam; Choi, Daniel

    2009-01-01

    Copper tubes having diameters between about 100 and about 200 nm have been fabricated by electrodeposition of copper into the pores of alumina nanopore membranes. Copper nanotubes are under consideration as alternatives to copper nanorods and nanowires for applications involving thermal and/or electrical contacts, wherein the greater specific areas of nanotubes could afford lower effective thermal and/or electrical resistivities. Heretofore, copper nanorods and nanowires have been fabricated by a combination of electrodeposition and a conventional expensive lithographic process. The present electrodeposition-based process for fabricating copper nanotubes costs less and enables production of copper nanotubes at greater rate.

  8. [Copper and the human body].

    Science.gov (United States)

    Krízek, M; Senft, V; Motán, J

    1997-11-19

    Copper is one of the essential trace elements. It is part of a number of enzymes. Deficiency of the element is manifested by impaired haematopoesis, bone metabolism, disorders of the digestive, cardiovascular and nervous system. Deficiency occurs in particular in patients suffering from malnutrition, malabsorption, great copper losses during administration of penicillamine. Sporadically copper intoxications are described (suicidal intentions or accidental ingestion of beverages with a high copper content). Acute exposure to copper containing dust is manifested by metal fume fever. Copper salts can produce local inflammations. Wilson's disease is associated with inborn impaired copper metabolism. In dialyzed patients possible contaminations of the dialyzate with copper must be foreseen as well as the possible release of copper from some dialyzation membranes. With the increasing amount of copper in the environment it is essential to monitor the contamination of the environment.

  9. Targeting copper in cancer therapy: 'Copper That Cancer'.

    Science.gov (United States)

    Denoyer, Delphine; Masaldan, Shashank; La Fontaine, Sharon; Cater, Michael A

    2015-11-01

    Copper is an essential micronutrient involved in fundamental life processes that are conserved throughout all forms of life. The ability of copper to catalyze oxidation-reduction (redox) reactions, which can inadvertently lead to the production of reactive oxygen species (ROS), necessitates the tight homeostatic regulation of copper within the body. Many cancer types exhibit increased intratumoral copper and/or altered systemic copper distribution. The realization that copper serves as a limiting factor for multiple aspects of tumor progression, including growth, angiogenesis and metastasis, has prompted the development of copper-specific chelators as therapies to inhibit these processes. Another therapeutic approach utilizes specific ionophores that deliver copper to cells to increase intracellular copper levels. The therapeutic window between normal and cancerous cells when intracellular copper is forcibly increased, is the premise for the development of copper-ionophores endowed with anticancer properties. Also under investigation is the use of copper to replace platinum in coordination complexes currently used as mainstream chemotherapies. In comparison to platinum-based drugs, these promising copper coordination complexes may be more potent anticancer agents, with reduced toxicity toward normal cells and they may potentially circumvent the chemoresistance associated with recurrent platinum treatment. In addition, cancerous cells can adapt their copper homeostatic mechanisms to acquire resistance to conventional platinum-based drugs and certain copper coordination complexes can re-sensitize cancer cells to these drugs. This review will outline the biological importance of copper and copper homeostasis in mammalian cells, followed by a discussion of our current understanding of copper dysregulation in cancer, and the recent therapeutic advances using copper coordination complexes as anticancer agents.

  10. Excited triplet state photophysics of the sulphonated aluminium phthalocyanines bound to human serum albumin.

    Science.gov (United States)

    Foley, M S; Beeby, A; Parker, A W; Bishop, S M; Phillips, D

    1997-03-01

    The binding of the sulphonated aluminum phthalocyanines to human serum albumin (HSA) in aqueous phosphate buffer solution at 25 degrees C has been studied by measuring the properties of the triplet excited states of these dyes. The triplet lifetimes were measured by triplet-triplet absorption flash photolysis. The triplet lifetime of the disulphonated AlS2Pc (2.5 microM) varies from 500 +/- 30 microseconds in the absence of protein to 1.100 microseconds and longer with HSA concentrations above 100 microM. Under identical conditions, the maximum triplet lifetimes of the mono-, tri- and tetrasulphonated compounds bound to HSA are shorter than those for the disulphonated species. The increase in the triplet state lifetimes is attributed to the ability of the bulk aqueous phase to interact with the sensitizer at the site of binding; the site of binding being dependent on the degree of sulphonation. For AlS2Pc and AlS3Pc at all HSA concentrations, and regardless of the degree of sulphonation, all the triplet state decay profiles follow simple pseudo-first-order kinetics. The exponential decay of the triplet phthalocyanine at all HSA concentrations is ascribed to the rapid association and dissociation of the phthalocyanine-HSA complex on the time-scales of the triplet state lifetimes. A simplified one-step binding model is utilized to describe the results. The association of AlS1Pc with HSA results in substantial quenching of the triplet state quantum yield, and a more complex model is required to analyze the results. The tetrasulphonated compound (AlS4Pc) binds to the protein at a site where it experiences some protection from the aqueous phase.

  11. Photodynamic effects of silicon phthalocyanines in model cells and tumors (Invited Paper)

    Science.gov (United States)

    Oleinick, Nancy L.; Zaidi, Syed I. A.; Rihter, Boris D.; Kenney, Malcolm E.; Clay, Marian E.; Antunez, Antonio R.; Mukhtar, Hasan

    1992-06-01

    A series of silicon and aluminum phthalocyanines is being investigated in this laboratory for their potential as photosensitizers for photodynamic tumor therapy (PDT). Of these, one of the silicon phthalocyanines [SiPc(OH)OSi(CH3)2(CH2)3N(CH3)2] (Pc IV) has proven to be highly efficient in a series of in vitro assays and in PDT in vivo. When compared to sulfonated or non-sulfonated aluminum phthalocyanine and/or Photofrin II, Pc IV produced greater effects at lower concentrations in a clonogenic assay with V79 cells, and in photoenhancement of lipid peroxidation in human erythrocyte membranes. Physiological responses of treated cells in vitro appeared similar to those produced by PDT with other sensitizers; however, the responses, such as the induction of apoptosis in murine lymphoma, occurred with greater efficiency when Pc IV served as photosensitizer. In order to evaluate the efficacy of Pc IV in vivo, the dye was suspended in corn oil or incorporated into liposomes and injected intraperitoneally into C3H mice bearing RIF-1 tumors. Pharmacokinetic studies showed efficient uptake of Pc IV into the tumor, as well as into liver and kidney. For PDT, tumors were irradiated with 675 nm light from an argon-pumped dye laser. Treatment of tumors up to 100 mm3 with 1.0 mg/kg Pc IV and 135 J/cm2 produced ablation of the tumor within 48 hours. Tumors > 200 mm3 could be ablated with 2.0 mg/kg Pc IV. The data suggest that Pc IV may be a highly efficient photosensitizer for tumor PDT.

  12. Photodynamic antimicrobial chemotherapy using zinc phthalocyanine derivatives in treatment of bacterial skin infection

    Science.gov (United States)

    Chen, Zhuo; Zhang, Yaxin; Wang, Dong; Li, Linsen; Zhou, Shanyong; Huang, Joy H.; Chen, Jincan; Hu, Ping; Huang, Mingdong

    2016-01-01

    Photodynamic antimicrobial chemotherapy (PACT) is an effective method for killing bacterial cells in view of the increasing problem of multiantibiotic resistance. We herein reported the PACT effect on bacteria involved in skin infections using a zinc phthalocyanine derivative, pentalysine β-carbonylphthalocyanine zinc (ZnPc-Lys). Compared with its anionic ZnPc counterpart, ZnPc-Lys showed an enhanced antibacterial efficacy in vitro and in an animal model of localized infection. Meanwhile, ZnPc-Lys was observed to significantly reduce the wound skin blood flow during wound healing, indicating an anti-inflammation activity. This study provides new insight on the mechanisms of PACT in bacterial skin infection.

  13. The study of laser induced fluorescence of tooth hard tissues with aluminum phthalocyanine nanoparticles

    Science.gov (United States)

    Farrakhova, D. S.; Kuznetsova, J. O.; Loschenov, V. B.

    2016-08-01

    This work is about the possibility of fluorescence diagnosis application with the use of aluminum phthalocyanine nanoparticles (nAlPc) in order to detect enamel microdamage. For the investigation, five human teeth samples of various age groups were removed for various reasons. The autofluorescence spectrums of these samples hard tissues and fluorescence spectrums of nAlPc mixed with enamel powder were obtained during the experiment. The research shows that sample pathogenic microflora causes nAlPc fluorescence. This fact will allow detecting enamel microdamage in future studies.

  14. Electrical Properties of Zn-Phthalocyanine and Poly (3-hexylthiophene Doped Nematic Liquid Crystal

    Directory of Open Access Journals (Sweden)

    Y. Karakuş

    2011-01-01

    Full Text Available An E7 coded nematic liquid crystal was doped with zinc phthalocyanine and poly (3-hexylthiophene. A variety of properties including relaxation time, absorption coefficient, and critical frequency of this doped system were investigated using impedance spectroscopy. The doped systems displayed increased absorption coefficients in the range 0.22–0.55 and relaxation times from 5.05×10−7 s to 3.59×10−6 s with a decrease in the critical frequency from 3.54 MHz to 2.048 MHz.

  15. Geometric and Electronic Structures at the Interface between Iron Phthalocyanine and Si (110)

    Institute of Scientific and Technical Information of China (English)

    JIN Dan; Ateeq ur Rehman; QIAN Hui-Qin; JIANG Li-Zhen; ZHANG Han-Jie; LI Hai-Yang; HE Pi-Mo; BAO Shi-Ning

    2011-01-01

    The geometric and electronic structures at the interface between iron phthalocyanine (FePc) and Si(llO) surface are studied by ultraviolet photoelectron spectroscopy and density functional theory (DFT) calculation. After FePc is deposited on Si(llO), the emission features are located at 2.56, 4.90, 7.90, 10.88eV below the Fermi level for monolayer and 2.73, 4.90, 7.74, 10.52eV below the Fermi level for multilayer. At the coverage of 1 ML, FePc molecules are adsorbed on the bridge site in a fiat-lying geometry with a 2.17 A separation between the molecule and the substrate. The molecular plane is bent due to the interaction between the adsorbate and the substrate.%The geometric and electronic structures at the interface between iron phthalocyanine (FePc) and Si(110) surface are studied by ultraviolet photoelectron spectroscopy and density functional theory (DFT) calculation.After FePc is deposited on Si(110),the emission features are located at 2.56,4.90,7.90,10.88eV below the Fermi level for monolayer and 2.73,4.90,7.74,10.52eV below the Fermi level for multilayer.At the coverage of 1ML,FePc molecules are adsorbed on the bridge site in a flat-lying geometry with a 2.17A separation between the molecule and the substrate.The molecular plane is bent due to the interaction between the adsorbate and the substrate.Metal phthalocyanine (MPc) and its derivatives have attracted a large amount of interest in the past couple of years.Phthalocyanine molecules have been extensively used as pigments,dyes and models of biologically important species such as porphyrins,hemoglobin,and chlorophyll.They have been used as the active elements in chemical sensors,[1-3] and are of great benefit for use in thin film transistors,[4-6]organic electronic devices[7-10] and solar cells.[11-14

  16. Structure and Morphology of Phthalocyanine Films Grown in Electrical Fields by Vapor Deposition

    Science.gov (United States)

    Zhu, Shen; Banks, C. E.; Frazier, D. O.; Penn, B.; Abdeldayem, H.; Hicks, R.; Burns, H. D.; Thompson, G. W.

    1999-01-01

    Phthalocyanine (Pc) films have been synthesized by vapor deposition on quartz substrates, some of which were coated with a very thin gold film before depositing Pc films. Electrical fields up to 6200 V/cm between a mech electrode and the substrate are introduced during film growth. These films have been characterized by x-ray diffraction and scanning electron microscopy. The molecular orientations and surface morphology of Pc films were changed under the electrical fields. The surface of these films grown without electrical field shows whisk-like morphology. When films are deposited under an electrical field, a dense film with flat surface is obtained.

  17. Kinetic Research on Catalytic Degradation of Rhodamine B with Cobalt Phthalocyanine Supported Mg-Al Hydrotalcite.

    Science.gov (United States)

    Xu, Minhong; Cao, Yongyong; Ma, Xinyue

    2016-01-01

    Rhodamine B dye wastewater was degraded using cobalt phthalocyanine supported Mg-Al hydrotal- cite and H₂O₂. The effects of H₂O₂, temperature and concentration of Rhodamine B on the reaction kinetics were studied. The results indicate that the degradation process conforms to the equation of first order kinetics. The fastest rate constant k observed was 66.2 x 10⁻⁴/min⁻¹ at 62.5 °C, and the correlation coefficient R2 was 0.99733.

  18. High mobility polymer gated organic field effect transistor using zinc phthalocyanine

    Indian Academy of Sciences (India)

    K R Rajesh; V Kannan; M R Kim; Y S Chae; J K Rhee

    2014-02-01

    Organic thin film transistors were fabricated using evaporated zinc phthalocyanine as the active layer. Parylene film prepared by chemical vapour deposition was used as the organic gate insulator. The annealing of the samples was performed at 120°C for 3 h. At room temperature, these transistors exhibit -type conductivity with field-effect mobilities ranging from 0.025–0.037 cm2/Vs and a (on/off) ratio of ∼ 103. The effect of annealing on transistor characteristics is discussed.

  19. Energy-level alignment at interfaces between manganese phthalocyanine and C60

    Directory of Open Access Journals (Sweden)

    Daniel Waas

    2017-04-01

    Full Text Available We have used photoelectron spectroscopy to determine the energy-level alignment at organic heterojunctions made of manganese phthalocyanine (MnPc and the fullerene C60. We show that this energy-level alignment depends upon the preparation sequence, which is explained by different molecular orientations. Moreover, our results demonstrate that MnPc/C60 interfaces are hardly suited for application in organic photovoltaic devices, since the energy difference of the two lowest unoccupied molecular orbitals (LUMOs is rather small.

  20. Single crystal growth in spin-coated films of polymorphic phthalocyanine derivative under solvent vapor

    Energy Technology Data Exchange (ETDEWEB)

    Higashi, T.; Ohmori, M.; Ramananarivo, M. F.; Fujii, A., E-mail: afujii@opal.eei.eng.osaka-u.ac.jp; Ozaki, M. [Division of Electrical, Electronic, and Information Engineering, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871 (Japan)

    2015-12-01

    The effects of solvent vapor on spin-coated films of a polymorphic phthalocyanine derivative were investigated. Growth of single crystal films via redissolving organic films under solvent vapor was revealed by in situ microscopic observations of the films. X-ray diffraction measurement of the films after exposing to solvent vapor revealed the phase transition of polymorphs under solvent vapor. The direction of crystal growth was clarified by measuring the crystal orientation in a grown monodomain film. The mechanism of crystal growth based on redissolving organic films under solvent vapor was discussed in terms of the different solubilities of the polymorphs.

  1. Single crystal growth in spin-coated films of polymorphic phthalocyanine derivative under solvent vapor

    Directory of Open Access Journals (Sweden)

    T. Higashi

    2015-12-01

    Full Text Available The effects of solvent vapor on spin-coated films of a polymorphic phthalocyanine derivative were investigated. Growth of single crystal films via redissolving organic films under solvent vapor was revealed by in situ microscopic observations of the films. X-ray diffraction measurement of the films after exposing to solvent vapor revealed the phase transition of polymorphs under solvent vapor. The direction of crystal growth was clarified by measuring the crystal orientation in a grown monodomain film. The mechanism of crystal growth based on redissolving organic films under solvent vapor was discussed in terms of the different solubilities of the polymorphs.

  2. Up-Conversion Luminescence of a High Soluble Zinc Phthalocyanine-Epoxy Derivative

    Institute of Scientific and Technical Information of China (English)

    沈悦; 夏义本; 陈精纬; 顾峰; 焦凤华; 张建成

    2004-01-01

    Synthesis and photoelectric properties of a high soluble zinc phthalocyanine-epoxy derivative are investigated.The derivative can be solubilized in convenient solvents, such as CH3OH, CH3CH2OH and H2O. The fluorescence and UV-visible analyses indicate that the ZnPc-epoxy derivative still maintains the plane structure which comes from Zn(4,4',4",4″′-ta)Pc and the derivative has obvious up-conversion luminescence in room temperature. The up-conversion luminescence can be explained by the selection rule depending on the two-photon absorption.

  3. Studies on Organic Solar Cells Composed of Fullerenes and Zinc-Phthalocyanines

    OpenAIRE

    Pfützner, Steffen

    2012-01-01

    This work deals with the investigation and research on organic solar cells. In the first part of this work we focus on the spectroscopical and electrical characterization of the acceptor molecule and fullerene derivative C70. In combination with the donor molecule zinc-phthalocyanines (ZnPc) we investigate C70 in flat and bulk heterojunction solar cells and compare the results with C60 as acceptor. The stronger and spectral broader thin film absorption of C70 and thus enhanced contribution to...

  4. The Influence of Substituent Orientation on the Photovoltaic Performance of Phthalocyanine-Sensitized Solar Cells

    OpenAIRE

    Tejerina, Lara; Martínez Díaz, M. Victoria; Nazeeruddin, Mohammad Khaja; Torres, Tomás

    2016-01-01

    This is the peer reviewed version of the following article:Chemistry - A European Journal 22.13 (2016): 4369-4373, which has been published in final form at http://dx.doi.org/10.1002/chem.201600166. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving Phthalocyanines (Pcs) are used as sensitizers in dye-sensitized solar cells (DSSCs) because of their stability and intense absorption in the red and near-IR regions. Impressive ...

  5. Photodynamic response of an endothelial hybridoma cell line using zinc(II) tetrasubstituted phthalocyanines

    Science.gov (United States)

    Cruse-Sawyer, Janet E.; Dixon, B.; Roberts, David J.; Griffiths, John; Brown, Stanley B.

    1995-03-01

    The EAhy 926 cell is a hybridoma line derived from human endothelium and A549/8 cells. They display stable endothelial characteristics and may provide an indication of how endothelial cells respond to photodynamic therapy. Cells were grown as monolayers, seeded at a density of 104 cells/35 mm dish, and then incubated with zinc (II) tetrasubstituted phthalocyanines (carboxylated, sulphonated, pyridinium or diethanolamine sulphonamide). After 24 hours, the cells were illuminated with laser light at 680 nm or 692 nm as appropriate. The response to each photosensitizer was evaluated using cell proliferation, clonogenicity, and release of tissue factor.

  6. CHARACTERIZATION OF MANGANESE PHTHALOCYANINE-Fe3O4 NANOPARTICLE COMPOSITE AND ITS ELECTROMAGNETORHEOLOGICAL FLUID

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    Manganese phthalocyanine (MnPc)-Fe3O4 nanoparticles composite was prepared and characterized. The results show that MnPc are complexed on the surface of Fe3O4 nanoparticles in the state of single molecule. There is effective composite between MnPc and Fe3O4 nanoparticles which can improve the antioxidization ability of Fe3O4 nanoparticles greatly. The composite was dispersed into chlorinated paraffin oil to form electromagnetorheological (EMR) fluid with high activity,and the EMR properties of this EMR fluid are studied.

  7. Iron phthalocyanine modified mesoporous titania nanoparticles for photocatalytic activity and CO2 capture applications.

    Science.gov (United States)

    Ramacharyulu, P V R K; Muhammad, Raeesh; Praveen Kumar, J; Prasad, G K; Mohanty, Paritosh

    2015-10-21

    An iron(II)phthalocyanine (Fepc) modified mesoporous titania (Fepc-TiO2) nanocatalyst with a specific surface area of 215 m(2) g(-1) has been synthesized by a hydrothermal method. Fepc-TiO2 degrades one of the highly toxic chemical warfare agents, sulfur mustard (SM), photocatalytically under sunlight with an exposure time of as low as 70 min. Furthermore, the mesoporous Fepc-TiO2 also captured 2.1 mmol g(-1) of CO2 at 273 K and 1 atm.

  8. Synthesis and Spectroscopic Properties of a Series of New tetra-Substituted Metal Phthalocyanines

    Institute of Scientific and Technical Information of China (English)

    YU Hai-ling; YANG Jin; FU Qiang; MA Ji-cheng; LI Wei-li

    2008-01-01

    A new class of metal phthalocyanines(MPcs)containing four 8-quinolinol(8-QH) derivative moieties were successfully synthesized and characterized by mass spectroscopy,IR, UV-Vis and element analysis,the results of which were consistent with the proposed structures.All of them can dissolve in common organic solvents.such as dichloromethane,chloroform,and acetone.The effect of metal ion on the absorption of Q band was studied with UV-Vis spectra.The fluorescent properties for those complexes were also investigated.

  9. A model system for carbohydrates interactions on single-crystalline Ru surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Thanh Nam

    2015-07-01

    In this thesis, I present a model system for carbohydrate interactions with single-crystalline Ru surfaces. Geometric and electronic properties of copper phthalocyanine (CuPc) on top of graphene on hexagonal Ru(0001), rectangular Ru(10 anti 10) and vicinal Ru(1,1, anti 2,10) surfaces have been studied. First, the Fermi surfaces and band structures of the three Ru surfaces were investigated by high-resolution angle-resolved photoemission spectroscopy. The experimental data and theoretical calculations allow to derive detailed information about the momentum-resolved electronic structure. The results can be used as a reference to understand the chemical and catalytic properties of Ru surfaces. Second, graphene layers were prepared on the three different Ru surfaces. Using low-energy electron diffraction and scanning tunneling microscopy, it was found that graphene can be grown in well-ordered structures on all three surfaces, hexagonal Ru(0001), rectangular Ru(10 anti 10) and vicinal Ru(1,1, anti 2,10), although they have different surface symmetries. Evidence for a strong interaction between graphene and Ru surfaces is a 1.3-1.7 eV increase in the graphene π-bands binding energy with respect to free-standing graphene sheets. This energy variation is due to the hybridization between the graphene pi bands and the Ru 4d electrons, while the lattice mismatch does not play an important role in the bonding between graphene and Ru surfaces. Finally, the geometric and electronic structures of CuPc on Ru(10 anti 10), graphene/Ru(10 anti 10), and graphene/Ru(0001) have been studied in detail. CuPc molecules can be grown well-ordered on Ru(10 anti 10) but not on Ru(0001). The growth of CuPc on graphene/Ru(10 anti 10) and Ru(0001) is dominated by the Moire pattern of graphene. CuPc molecules form well-ordered structures with rectangular unit cells on graphene/Ru(10 anti 10) and Ru(0001). The distance of adjacent CuPc molecules is 15±0.5 Aa and 13±0.5 Aa on graphene/Ru(0001

  10. Power losses in bilayer inverted small molecule organic solar cells

    KAUST Repository

    Trinh, Cong

    2012-01-01

    Inverted bilayer organic solar cells using copper phthalocyanine (CuPc) as a donor and C60 as an acceptor with the structure: glass/indium tin oxide (ITO)/ZnO/C60/CuPc/MoO3/Al, in which the zinc oxide (ZnO) was deposited by atomic layer deposition, are compared with a conventional device: glass/ITO/CuPc/C60/bathocuproine/Al. These inverted and conventional devices give short circuit currents of 3.7 and 4.8 mA/cm 2, respectively. However, the inverted device gives a reduced photoresponse from the CuPc donor compared to that of the conventional device. Optical field models show that the arrangement of organic layers in the inverted devices leads to lower absorption of long wavelengths by the CuPc donor; the low energy portion of the spectrum is concentrated near the metal oxide electrode in both devices. © 2012 American Institute of Physics.

  11. Remarkable reduction in the threshold voltage of pentacene-based thin film transistors with pentacene/CuPc sandwich configuration

    Directory of Open Access Journals (Sweden)

    Yi Li

    2014-06-01

    Full Text Available This study investigates the remarkable reduction in the threshold voltage (VT of pentacene-based thin film transistors with pentacene/copper phthalocyanine (CuPc sandwich configuration. This reduction is accompanied by increased mobility and lowered sub-threshold slope (S. Sandwich devices coated with a 5 nm layer of CuPc layer are compared with conventional top-contact devices, and results indicate that VT decreased significantly from −20.4 V to −0.2 V, that mobility increased from 0.18 cm2/Vs to 0.51 cm2/Vs, and that S was reduced from 4.1 V/dec to 2.9 V/dec. However, the on/off current ratio remains at 105. This enhanced performance could be attributed to the reduction in charge trap density by the incorporated CuPc layer. Results suggest that this method is simple and effectively generates pentacene-based organic thin film transistors with high mobility and low VT.

  12. Probing of Charge Transfer States at Buried Organic Interfaces with Even-Order Spectroscopy

    Science.gov (United States)

    Pandey, Ravindra; Moon, Aaron; Roberts, Sean

    Organic thin film photovoltaics (OPV) are an emerging economically competitive technology that combines manufacturing adaptability, low-cost processing and a lightweight, flexible device end-product. At junctions formed between organic electron-donating and electron-accepting materials, the abrupt change in the dielectric properties can strongly perturb the density of states of the OPV. This can substantially alter the driving force for charge transfer between these materials. Electronic Sum Frequency Generation (ESFG), owing to its inherent interfacial sensitivity, is ideally suited to probe buried interfaces. Here, we report the ESFG spectra of Copper Phthalocyanine (CuPc) films, deposited on SiO2 measured for both reflection and transmission geometries. Three peaks are observed that roughly correlate with resonances that comprise CuPc's Q-band absorption but display slight shifts and amplitude changes with respect to CuPc's bulk absorption spectrum. Experimental results are compared with calculations based on a thin film interference model that accounts for ESFG emitted from both the CuPc:Air and CuPc:SiO2 interface as well as contributions to the signal from higher order source terms from the bulk. The model reveals a difference in the density of states between the two interfaces and suggests that by combining experimental transmission and reflection data it is possible to separate bulk and interfacial contributions to ESFG spectra.

  13. The importance of gap states for energy level alignment at hybrid interfaces

    Energy Technology Data Exchange (ETDEWEB)

    Racke, D.A.; Kelly, L.L.; Monti, O.L.A., E-mail: monti@u.arizona.edu

    2015-10-01

    Highlights: • The electronic structure of CuPc on related layered van der Waals materials is compared. • Gap states need to be considered to understand energy level alignment. • Hybrid interfaces require new models of the interfacial electronic structure. - Abstract: Energy level alignment and electronic structure at organic semiconductor interfaces must be controlled to ensure efficient carrier harvesting or injection in next-generation organic optoelectronic technologies. In this context, hybrid organic/inorganic semiconductor interfaces exhibit particularly rich physics. Here, we show that states in the band gap of the inorganic layered van der Waals dichalcogenide SnS{sub 2} play an important role in determining energy level alignment at the hybrid interface with copper phthalocyanine (CuPc). By taking advantage of the closely related CuPc film growth on SnS{sub 2} and the well-studied interface of CuPc/HOPG, we are able to trace spectroscopic differences to the fundamentally different electronic interactions across the two interfaces. We provide a detailed picture of the role of gap states at the hybrid interface and shed light on the electronic properties of inorganic semiconductors in general and metal dichalcogenides in particular.

  14. Photoconductivity of thin organic films

    Science.gov (United States)

    Tkachenko, Nikolai V.; Chukharev, Vladimir; Kaplas, Petra; Tolkki, Antti; Efimov, Alexander; Haring, Kimmo; Viheriälä, Jukka; Niemi, Tapio; Lemmetyinen, Helge

    2010-04-01

    Thin organic films were deposited on silicon oxide surfaces with golden interdigitated electrodes (interelectrode gap was 2 μm), and the film resistivities were measured in dark and under white light illumination. The compounds selected for the measurements include molecules widely used in solar cell applications, such as polythiophene ( PHT), fullerene ( C60), pyrelene tetracarboxylic diimide ( PTCDI) and copper phthalocyanine ( CuPc), as well as molecules potentially interesting for photovoltaic applications, e.g. porphyrin-fullerene dyads. The films were deposited using thermal evaporation (e.g. for C60 and CuPc films), spin coating for PHT, and Langmuir-Schaeffer for the layer-by-layer deposition of porphyrin-fullerene dyads. The most conducting materials in the series are films of PHT and CuPc with resistivities 1.2 × 10 3 Ω m and 3 × 10 4 Ω m, respectively. Under light illumination resistivity of all films decreases, with the strongest light effect observed for PTCDI, for which resistivity decreases by 100 times, from 3.2 × 10 8 Ω m in dark to 3.1 × 10 6 Ω m under the light.

  15. Photoconductivity of thin organic films

    Energy Technology Data Exchange (ETDEWEB)

    Tkachenko, Nikolai V. [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FIN-33101 Tampere (Finland); Chukharev, Vladimir, E-mail: Vladimir.Chukharev@tut.fi [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FIN-33101 Tampere (Finland); Kaplas, Petra; Tolkki, Antti; Efimov, Alexander [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FIN-33101 Tampere (Finland); Haring, Kimmo; Viheriaelae, Jukka; Niemi, Tapio [Optoelectronics Research Centre, Tampere University of Technology, P.O. Box 692, FIN-33101 Tampere (Finland); Lemmetyinen, Helge [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FIN-33101 Tampere (Finland)

    2010-04-01

    Thin organic films were deposited on silicon oxide surfaces with golden interdigitated electrodes (interelectrode gap was 2 {mu}m), and the film resistivities were measured in dark and under white light illumination. The compounds selected for the measurements include molecules widely used in solar cell applications, such as polythiophene (PHT), fullerene (C{sub 60}), pyrelene tetracarboxylic diimide (PTCDI) and copper phthalocyanine (CuPc), as well as molecules potentially interesting for photovoltaic applications, e.g. porphyrin-fullerene dyads. The films were deposited using thermal evaporation (e.g. for C{sub 60} and CuPc films), spin coating for PHT, and Langmuir-Schaeffer for the layer-by-layer deposition of porphyrin-fullerene dyads. The most conducting materials in the series are films of PHT and CuPc with resistivities 1.2 x 10{sup 3} {Omega} m and 3 x 10{sup 4} {Omega} m, respectively. Under light illumination resistivity of all films decreases, with the strongest light effect observed for PTCDI, for which resistivity decreases by 100 times, from 3.2 x 10{sup 8} {Omega} m in dark to 3.1 x 10{sup 6} {Omega} m under the light.

  16. Fabrication and characterization of inverted organic solar cells using shuttle cock-type metal phthalocyanine and PCBM:P3HT

    Energy Technology Data Exchange (ETDEWEB)

    Suzuki, Atsushi, E-mail: suzuki@mat.usp.ac.jp; Furukawa, Ryo, E-mail: suzuki@mat.usp.ac.jp; Akiyama, Tsuyoshi, E-mail: suzuki@mat.usp.ac.jp; Oku, Takeo, E-mail: suzuki@mat.usp.ac.jp [Department of Materials Science, The University of Shiga Prefecture 2500 Hassaka, Hikone, Shiga 522-8533 (Japan)

    2015-02-27

    Inverted organic solar cells using shuttle cock-type phthalocyanine, semiconducting polymer and fullerenes were fabricated and characterized. Photovoltaic and optical properties of the solar cells with inverted structures were investigated by optical absorption, current density-voltage characteristics. The photovoltaic properties of the tandem organic solar cell using titanyl phthalocyanine, vanadyl phthalocyanine, poly(3-hexylthiophene) (P3HT) and [6, 6]-phenyl C{sub 61}-butyric acid methyl ester (PCBM) were improved. Effect of annealing and solvent treatment on surface morphologies of the active layer was investigated. The photovoltaic mechanisms, energy levels and band gap of active layers were discussed for improvement of the photovoltaic performance.

  17. LEP copper accelerating cavities

    CERN Multimedia

    Laurent Guiraud

    1999-01-01

    These copper cavities were used to generate the radio frequency electric field that was used to accelerate electrons and positrons around the 27-km Large Electron-Positron (LEP) collider at CERN, which ran from 1989 to 2000. The copper cavities were gradually replaced from 1996 with new superconducting cavities allowing the collision energy to rise from 90 GeV to 200 GeV by mid-1999.

  18. Copper wire bonding

    CERN Document Server

    Chauhan, Preeti S; Zhong, ZhaoWei; Pecht, Michael G

    2014-01-01

    This critical volume provides an in-depth presentation of copper wire bonding technologies, processes and equipment, along with the economic benefits and risks.  Due to the increasing cost of materials used to make electronic components, the electronics industry has been rapidly moving from high cost gold to significantly lower cost copper as a wire bonding material.  However, copper wire bonding has several process and reliability concerns due to its material properties.  Copper Wire Bonding book lays out the challenges involved in replacing gold with copper as a wire bond material, and includes the bonding process changes—bond force, electric flame off, current and ultrasonic energy optimization, and bonding tools and equipment changes for first and second bond formation.  In addition, the bond–pad metallurgies and the use of bare and palladium-coated copper wires on aluminum are presented, and gold, nickel and palladium surface finishes are discussed.  The book also discusses best practices and re...

  19. Combination of hyperthermia and photodynamic therapy on mesenchymal stem cell line treated with chloroaluminum phthalocyanine magnetic-nanoemulsion

    Science.gov (United States)

    de Paula, Leonardo B.; Primo, Fernando L.; Pinto, Marcelo R.; Morais, Paulo C.; Tedesco, Antonio C.

    2015-04-01

    The present study reports on the preparation and the cell viability assay of two nanoemulsions loaded with magnetic nanoparticle and chloroaluminum phthalocyanine. The preparations contain equal amount of chloroaluminum phthalocyanine (0.05 mg/mL) but different contents of magnetic nanoparticle (0.15×1013 or 1.50×1013 particle/mL). The human bone marrow mesenchymal stem cell line was used as the model to assess the cell viability and this type of cell can be used as a model to mimic cancer stem cells. The cell viability assays were performed in isolated as well as under combined magnetic hyperthermia and photodynamic therapy treatments. We found from the cell viability assay that under the hyperthermia treatment (1 MHz and 40 Oe magnetic field amplitude) the cell viability reduction was about 10%, regardless the magnetic nanoparticle content within the magnetic nanoparticle/chloroaluminum phthalocyanine formulation. However, cell viability reduction of about 50% and 60% were found while applying the photodynamic therapy treatment using the magnetic nanoparticle/chloroaluminum phthalocyanine formulation containing 0.15×1013 or 1.50×1013 magnetic particle/mL, respectively. Finally, an average reduction in cell viability of about 66% was found while combining the hyperthermia and photodynamic therapy treatments.

  20. Self-Assembly of Individually Addressable Complexes of C-60 and Phthalocyanines on a Metal Surface : Structural and Electronic Investigations

    NARCIS (Netherlands)

    Samuely, Tomas; Liu, Shi-Xia; Haas, Marco; Decurtins, Silvio; Jung, Thomas A.; Stoehr, Meike

    2009-01-01

    The hosting properties of a close-packed layer of phenoxy-substituted phthalocyanine derivatives adsorbed on Ag(III) were investigated for the adsorption of C-60 molecules. The C-60 molecules bind to two clearly distinguishable sites, namely, to the underlying metal substrate in between two adjacent

  1. The synthesis and photophysical properties of novel cationic tetra pyridiloxy substituted aluminium, silicon and titanium phthalocyanines in water

    Energy Technology Data Exchange (ETDEWEB)

    Masilela, Nkosiphile [Department of Chemistry, Rhodes University, Grahamstown 6140 (South Africa); Nyokong, Tebello, E-mail: t.nyokong@ru.ac.z [Department of Chemistry, Rhodes University, Grahamstown 6140 (South Africa)

    2010-10-15

    This work reports on the synthesis, characterisation and photophysical properties of new unquaternized {beta}-2,(3)-tetra-(2 pyridiloxy) aluminium(III) (3a), silicon(IV) (3b), titanium(IV) (3c) phthalocyanines and their water-soluble quaternized counterparts, 4a, 4b and 4c, respectively. The water-soluble silicon(IV) (4b) and titanium(IV) (4c) phthalocyanine derivatives were found to be aggregated in aqueous media but were partially or fully disaggregated in the presence of a surfactant Cremophor EL (CEL). The photophysical properties of aggregated complexes were investigated both in the presence of CEL and in pH 11 alone. Low triplet and fluorescence yield were obtained in pH 11 but an improvement was achieved upon addition of CEL for the aggregated complexes. The unquaternized silicon(IV) phthalocyanine complex (3b) gave the highest triplet quantum yield of 0.77 in DMF followed by its quaternized derivative (4b) with triplet yield of 0.73 in pH 11 plus CEL. The highest triplet lifetime of 220 {mu}s was obtained for 4b in the presence of CEL. Higher fluorescence yields of 0.23 were obtained for quaternized water-soluble aluminium(III) phthalocyanine derivative (4a) in the presence of CEL.

  2. Raman spectra of zinc phthalocyanine monolayers absorbed on glassy carbon and gold electrodes by application of a confocal Raman microspectrometer

    NARCIS (Netherlands)

    Palys-Staron, B.J.; Palys, B.J.; Puppels, G.J.; Puppels, G.J.; van den Ham, D.M.W.; van den Ham, D.M.W.; Feil, D.; Feil, D.

    1992-01-01

    Raman spectra of zinc phthalocyanine monolayers, adsorbed on gold and on glassy carbon surfaces (electrodes), are presented. These spectra have been recorded with the electrodes inside and outside an electrochemical cell filled with an aqueous electrolyte. A confocal Raman microspectrometer was

  3. A first archetype of boron dipyrromethene-phthalocyanine pentad dye: design, synthesis, and photophysical and photochemical properties.

    Science.gov (United States)

    Göl, Cem; Malkoç, Mustafa; Yeşilot, Serkan; Durmuş, Mahmut

    2014-05-28

    A novel type of phthalocyanine pentad containing four boron dipyrromethene (BODIPY) units at peripheral positions of the phthalocyanine framework has been designed and synthesized for the first time. The Sonogashira coupling reaction between 4,4'-difluoro-8-(4-ethynyl)-phenyl-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene (Ethynyl-BODIPY) and 2(3),9(10),16(17),23(24)-tetrakis(iodo) zinc(ii) phthalocyanine (Iodo-Pc) has been used for the synthesis of the target compound. The BODIPY-phthalocyanine pentad dye (BODIPY-Pc) has been fully characterized by (1)H NMR, MALDI-TOF mass, FT-IR and UV-Vis spectroscopic techniques and elemental analysis as well. The photoinduced energy transfer process for this dye system was explored in tetrahydrofuran solution. The singlet oxygen generation capability and photodegradation behaviours of this BODIPY-Pc pentad dye were also investigated in DMSO for the determination of the usability of this new type of dye system as a photosensitizer in PDT applications.

  4. Effect of axial ligands on the spectroelectrochemical properties of zinc phthalocyanine films. In situ Raman and electroreflection spectra

    NARCIS (Netherlands)

    Palys, B.J.; Ham, van den D.M.W.; Otto, C.

    1994-01-01

    Electroreflection and Raman spectra (in situ and ex situ) of zinc phthalocyanine (ZnPc) films (80 nm thick) have been studied. Raman spectra were resonantly and preresonantly enhanced. Both electroreflection and Raman experiments reveal the homogeneous inclusion of electrolyte anions upon oxidation

  5. Self-Assembly of Individually Addressable Complexes of C-60 and Phthalocyanines on a Metal Surface : Structural and Electronic Investigations

    NARCIS (Netherlands)

    Samuely, Tomas; Liu, Shi-Xia; Haas, Marco; Decurtins, Silvio; Jung, Thomas A.; Stoehr, Meike

    2009-01-01

    The hosting properties of a close-packed layer of phenoxy-substituted phthalocyanine derivatives adsorbed on Ag(III) were investigated for the adsorption of C-60 molecules. The C-60 molecules bind to two clearly distinguishable sites, namely, to the underlying metal substrate in between two adjacent

  6. Slow Structural Rearrangement of a Side-Chain Phthalocyanine Methacrylate Polymer at the Air-Water Interface

    NARCIS (Netherlands)

    Nostrum, C.F. van; Nolte, R.J.M.; Devillers, M.A.C.; Oostergetel, G.T.; Teerenstra, M.N.; Schouten, A.J.

    1993-01-01

    A polymethacrylate with dodecoxy-substituted phthalocyanine units in the side chains has been used to form Langmuir-Blodgett monolayers at the air-water interface. The monolayers are highly crystalline. They expand slowly even when a constant surface pressure is applied. The structural change

  7. Iron phthalocyanine supported on amidoximated PAN fiber as effective catalyst for controllable hydrogen peroxide activation in oxidizing organic dyes.

    Science.gov (United States)

    Han, Zhenbang; Han, Xu; Zhao, Xiaoming; Yu, Jiantao; Xu, Hang

    2016-12-15

    Iron(II) phthalocyanine was immobilized onto amidoximated polyacrylonitrile fiber to construct a bioinspired catalytic system for oxidizing organic dyes by H2O2 activation. The amidoxime groups greatly helped to anchor Iron(II) phthalocyanine molecules onto the fiber through coordination interaction, which has been confirmed by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and UV-vis diffuse reflectance spectroscopy analyses. Electron spin resonance studies indicate that the catalytic process of physically anchored Iron(II) phthalocyanine performed via a hydroxyl radical pathway, while the catalyst bonded Iron(II) phthalocyanine through coordination effect could selectively catalyze the H2O2 decomposition to generate high-valent iron-oxo species. This may result from the amidoxime groups functioning as the axial fifth ligands to favor the heterolytic cleavage of the peroxide OO bond. This feature also enables the catalyst to only degrade the dyes adjacent to the catalytic active centers and enhances the efficient utilization of H2O2. In addition, this catalyst could effectively catalyze the mineralization of organic dyes and can be easily recycled without any loss of activity. Copyright © 2016 Elsevier B.V. All rights reserved.

  8. Crystal fields of porphyrins and phthalocyanines from polarization-dependent 2p-to-3d multiplets

    DEFF Research Database (Denmark)

    Johnson, Phillip S.; García Lastra, Juan Maria; Kennedy, Colton K.;

    2014-01-01

    Polarization-dependent X-ray absorption spectroscopy is combined with density functional calculations and atomic multiplet calculations to determine the crystal field parameters 10Dq, Ds, and Dt of transition metal phthalocyanines and octaethylporphyrins (Mn, Fe, Co, Ni). The polarization...

  9. Synthesis, properties and drug potential of the photosensitive alkyl- and alkylsiloxy-ligated silicon phthalocyanine Pc 227.

    Science.gov (United States)

    Li, Jun; Yang, Yang; Zhang, Ping; Sounik, James R; Kenney, Malcolm E

    2014-12-01

    The photosensitive, alkyl- and alkylsiloxy-ligated silicon phthalocyanine, SiPc[(CH2)3SH][OSi(CH3)2(CH2)3N(CH3)2], Pc 227, has been prepared and characterized. This phthalocyanine yields the experimental photodynamic therapy (PDT) drug Pc 4, SiPc[OH][OSi(CH3)2(CH2)3N(CH3)2], when irradiated with red light. To provide an understanding of the process by which Pc 227 and other alkyl-alkylsiloxysilicon phthalocyanines such as Pc 227 are photolyzed, bond dissociation energy, natural bond orbital (NBO) charge distribution, spin density distribution, nucleus-independent chemical shift (NICS), and electron localization function (ELF) calculations have been carried out on two models related to it. These show that the lowest energy pathway for the photolysis of Pc 227 is a homolysis involving a phthalocyanine π radical having a low SiPc-C bond dissociation energy. The promise of the results of this study for synthetic chemistry and drug development is discussed.

  10. Standard Specification for Copper-Aluminum-Silicon-Cobalt Alloy, Copper-Nickel-Silicon-Magnesium Alloy, Copper-Nickel-Silicon Alloy, Copper-Nickel-Aluminum-Magnesium Alloy, and Copper-Nickel-Tin Alloy Sheet and Strip

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2015-01-01

    Standard Specification for Copper-Aluminum-Silicon-Cobalt Alloy, Copper-Nickel-Silicon-Magnesium Alloy, Copper-Nickel-Silicon Alloy, Copper-Nickel-Aluminum-Magnesium Alloy, and Copper-Nickel-Tin Alloy Sheet and Strip

  11. Phthalocyanine dye as an extremely photostable and highly fluorescent near-infrared labeling reagent

    Science.gov (United States)

    Peng, Xinzhan; Draney, Daniel R.; Volcheck, William M.; Bashford, Gregory R.; Lamb, Donald T.; Grone, Daniel L.; Zhang, Yonghong; Johnson, Craig M.

    2006-02-01

    Current organic fluorophores used as labeling reagents for biomolecule conjugation have significant limitations in photostability. This compromises their performance in applications that require a photostable fluorescent reporting group. For example, in molecular imaging and single molecule microscopy, photostable fluorescent labels are important for observing and tracking individual molecular events over extended period of time. We report in this paper an extremely photostable and highly fluorescent phthalocyanine dye, IRDye TM 700DX, as a near-infrared fluorescence labeling reagent to conjugate with biomolecules. This novel water-soluble silicon phthalocyanine dye has an isomericly pure chemical structure. The dye is about 45 to 128 times more photostable than current near-IR fluorophores, e.g. Alexa Fluor"R"680, Cy TM 5.5, Cy TM 7 and IRDye TM 800CW dyes; and about 27 times more photostable than tetramethylrhodamine (TMR), one of the most photostable organic dyes. This dye also meets all the other stringent requirements as an ideal fluorophore for biomolecules labeling such as excellent water solubility, no aggregation in high ionic strength buffer, large extinction coefficient and high fluorescent quantum yield. Antibodies conjugated with IRDye TM 700DX at high D/P ratio exist as monomeric species in high ionic buffer and have bright fluorescence. The IRDye TM 700DX conjugated antibodies generate sensitive, highly specific detection with very low background in Western blot and cytoblot assays.

  12. Investigation in morphology and optical properties of electron beam gun evaporated nanostructured Bromoindium phthalocyanine thin films

    Science.gov (United States)

    Azim-Araghi, M. E.; Sahebi, R.

    2014-01-01

    Bromoindium phthalocyanine in thin film form was prepared by electron beam gun evaporation technique, using pre-cleaned polyborosilicate glass as substrate. 2D AFM image confirms that the surface of BrInPc thin film is granular with a grain size of 40-60 nm. 3D AFM image confirms that surface is homogeneous and its RMS roughness is 4.9 nm. The UV-VIS absorption spectrum showed two well-known absorption bands of the phthalocyanines, B and Q bands and characteristics Davydov splitting were observed. The optical transition determined to be direct allowed and the value of optical band gap was obtained. The value of Urbach energy was calculated. To investigation in the effect of thermal annealing on optical properties of BrInPc thin films, we annealed some thin films at 473 and 603 K for 1 h. As the result of thermal annealing we observed another absorption peak, named N-band, in absorption spectrum. A red shift observed in the position of B-band and Q-band peaks. There was not changing in optical transition mechanism. The value of optical band gap decreased and the Urbach energy increased as the result of thermal annealing.

  13. Preparation of Organic Zn-Phthalocyanine-Based Semiconducting Materials and Their Optical and Electrochemical Characterization

    Directory of Open Access Journals (Sweden)

    Amira Hajri

    2013-01-01

    Full Text Available In order to increase the species of organic semiconductors, new Zn-phthalocyanines-based organic materials were synthesized and characterized. The new compounds have been characterized by 1H and 13C using NMR, FTIR, and UV-Vis. The absorption, fluorescence, and electrochemical properties were also studied. Green photoluminescence was observed in dilute solutions. In solid thin films, π-π* interactions influenced the optical properties, and redshifted photoluminescence spectra were obtained; red emissions for ZnPAL (647 nm and ZnPTr (655 nm were found. By cyclic voltammetry, the electrochemical band gap was estimated to be 1.94 and 1.17 eV for ZnPAl and ZnPTr, respectively. Single-layer diode devices of an indium tin oxide/Zn-phthalocyanine/aluminum configuration were fabricated and showed relatively low turn-on voltages (3.3 V for ZnPAl and 3 V for ZnPTr.

  14. Characterization of crystal polymorphs of the organic semiconductor non-peripheral octa-hexyl phthalocyanine

    Science.gov (United States)

    Yoneya, Makoto; Miyamoto, Ayano; Shimizu, Yo; Ohmori, Masashi; Fujii, Akihiko; Ozaki, Masanori

    2017-08-01

    The carrier-transport and thermodynamic properties of two crystal polymorphs, i.e., bulk and needle polymorphs, of non-peripheral octa-hexyl substituted phthalocyanine were investigated using density functional theory calculations and molecular dynamics simulations. The calculated results show that the bulk and needle polymorphs have hole mobilities of the same order of magnitude and that the hole mobility of the bulk polymorph was approximately twice that of the needle polymorph. For ideal one-dimensional transport along π stacking columns, the difference in mobility between the two polymorphs was larger by a factor of approximately 8. Therefore, we can expect the bulk polymorph to have 2 (or 8) times higher mobility than the values for the needle polymorph. These results predict that the bulk polymorph has the potential to show higher device performance than the needle polymorph. We also obtained the results that imply that a needle-polymorph-like phase with uniform (monoclinic) phthalocyanine-core tilting (instead of the alternative tilting of the needle polymorph) could be a new polymorph in this crystal system.

  15. Distribution and retention of rose bengal and disulphonated aluminium phthalocyanine: a comparative study in unicellular eukaryote.

    Science.gov (United States)

    Croce, A C; Wyroba, E; Bottiroli, G

    1992-12-01

    Enhanced video-fluorescence microscopy and microspectrofluorometry were used to characterize the internalization, distribution and retention of two photosensitizers, rose bengal--a xanthene dye--and disulphonated aluminium phthalocyanine in eukaryote Paramecium aurelia. Rose bengal, because of its anionic nature, cannot diffuse across the cell membrane and accumulates there preferentially. In a drug-free medium the membrane fluorescence disappears after a few minutes. Complexation of rose bengal with low density lipoproteins gives rise to a different fluorescence pattern, where, in addition to membrane localization and diffuse cytoplasmic fluorescence, highly fluorescent endosomes are observed, which persisted for at least 1 h after drug treatment. Disulphonated aluminium phthalocyanine, on the contrary, seems to be directly internalized through an endocytotic process leading to the appearance of fluorescent endosomes, exhibiting a long persistence, together with cytoplasmic diffuse fluorescence. The presence of low density lipoproteins does not modify the internalization of the drug significantly, because of the very low yield of the complexation reaction. The potential of rose bengal as a photosensitizer for photodynamic therapy is discussed.

  16. Enhanced electrochemical sensing of thiols based on cobalt phthalocyanine immobilized on nitrogen-doped graphene.

    Science.gov (United States)

    Xu, Huiying; Xiao, Jingjing; Liu, Baohong; Griveau, Sophie; Bedioui, Fethi

    2015-04-15

    A hybrid nanocomposite based on cobalt phthalocyanine (CoPc) immobilized on nitrogen-doped graphene (N-G) (N-G/CoPc) has been developed to modify glassy carbon electrode (GCE) for the sensitive detection of thiols. The nanocomposites were characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemical impedance spectroscopy (EIS). Cyclic voltammetric studies showed that cobalt phthalocyanine and nitrogen doped graphene have a synergic effect and significantly enhance the electrocatalytic activity of the modified electrode towards thiols oxidation compared with electrodes modified with solely CoPc or N-G. The electrochemical oxidation responses were studied and the reaction mechanisms were discussed. The sensors exhibited a wide linear response range from 1μΜ to 16mM and a low detection limit of 1μΜ for the determination of l-cysteine, reduced l-glutathione and 2-mercaptoethanesulfonic acid in alkaline aqueous solution. The proposed N-G/CoPc hybrids contribute to the construction of rapid, convenient and low-cost electrochemical sensors for sensitive detection of thiols. Copyright © 2014 Elsevier B.V. All rights reserved.

  17. A zinc phthalocyanine based periodic mesoporous organosilica exhibiting charge transfer to fullerenes.

    Science.gov (United States)

    Auras, Florian; Li, Yan; Löbermann, Florian; Döblinger, Markus; Schuster, Jörg; Peter, Laurence M; Trauner, Dirk; Bein, Thomas

    2014-11-10

    Periodic mesoporous organosilica (PMO) materials offer a strategy to position molecular semiconductors within a highly defined, porous network. We developed thin films of a new semiconducting zinc phthalocyanine-bridged PMO exhibiting a face-centered orthorhombic pore structure with an average pore diameter of 11 nm. The exceptional degree of order achieved with this PMO enabled us to create thin films consisting of a single porous domain throughout their entire thickness, thus providing maximal accessibility for subsequent incorporation of a complementary phase. The phthalocyanine building blocks inside the pore walls were found to be well-aggregated, enabling electronic conductivity and extending the light-harvesting capabilities to the near IR region. Ordered 3D heterojunctions capable of promoting photo-induced charge transfer were constructed by impregnation of the PMO with a fullerene derivative. When integrated into a photovoltaic device, the infiltrated PMO is capable of producing a high open-circuit voltage and a considerable photocurrent, which represents a significant step towards potential applications of PMOs in optoelectronics. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Excitation dependent bidirectional electron transfer in phthalocyanine-functionalised MoS2 nanosheets.

    Science.gov (United States)

    Nguyen, Emily P; Carey, Benjamin J; Harrison, Christopher J; Atkin, Paul; Berean, Kyle J; Della Gaspera, Enrico; Ou, Jian Zhen; Kaner, Richard B; Kalantar-Zadeh, Kourosh; Daeneke, Torben

    2016-09-15

    Two-dimensional (2D) transition metal chalcogenides such as 2D MoS2 are considered prime candidate materials for the design of next generation optoelectronics. Functionalisation of these materials is considered to be a key step in tailoring their properties towards specific applications and unlocking their full potential. Here we present a van der Waals functionalisation strategy for creating MoS2 nanosheets decorated with free base phthalocyanine chromophores. The semiconducting sheets are found to intimately interact with these optoelectronically active chromophores, resulting in an electronic heterostructure that exhibits enhanced optoelectronic properties and exploitable charge transfer. We show that by utilising laterally confined MoS2 nanosheets, the conduction band of the semiconductor could be positioned between the chromophore's S1 and S2 states. Consequently, bidirectional photoinduced electron transfer processes are observed, with excitation of the functionalised nanosheet's semiconductor transition resulting in electron transfer to the phthalocyanine's LUMO, and excitation of the chromophore's S2 state leading to electron injection into the MoS2 conduction band. However, charge transfer from the dye's S1 transition to the MoS2 nanosheet is found to be thermodynamically unfavourable, resulting in intense radiative recombination. These findings may enable controlling and tuning the charge carrier density of semiconducting nanosheets via optical means through the exploitation of photoinduced electron transfer. Furthermore this work provides access to 2D semiconductor-hybrids with tailored absorption profiles and photoluminescence.

  19. Flexible heterostructures based on metal phthalocyanines thin films obtained by MAPLE

    Science.gov (United States)

    Socol, M.; Preda, N.; Rasoga, O.; Breazu, C.; Stavarache, I.; Stanculescu, F.; Socol, G.; Gherendi, F.; Grumezescu, V.; Popescu-Pelin, G.; Girtan, M.; Stefan, N.

    2016-06-01

    Heterostructures based on zinc phthalocyanine (ZnPc), magnesium phthalocyanine (MgPc) and 5,10,15,20-tetra(4-pyrydil)21H,23H-porphine (TPyP) were deposited on ITO flexible substrates by Matrix Assisted Pulsed Laser Evaporation (MAPLE) technique. Organic heterostructures containing (TPyP/ZnPc(MgPc)) stacked or (ZnPc(MgPc):TPyP) mixed layers were characterized by X-ray diffraction-XRD, photoluminescence-PL, UV-vis and FTIR spectroscopy. No chemical decomposition of the initial materials was observed. The investigated structures present a large spectral absorption in the visible range making them suitable for organic photovoltaics applications (OPV). Scanning electron microscopy-SEM and atomic force microscopy-AFM revealed morphologies typical for the films prepared by MAPLE. The current-voltage characteristics of the investigated structures, measured in dark and under light, present an improvement in the current value (∼3 order of magnitude larger) for the structure based on the mixed layer (Al/MgPc:TPyP/ITO) in comparison with the stacked layer (Al/MgPc//TPyP/ITO). A photogeneration process was evidenced in the case of structures Al/ZnPc:TPyP/ITO with mixed layers.

  20. Absorption induced modulation of magnetism in two-dimensional metal-phthalocyanine porous sheets.

    Science.gov (United States)

    Zhou, Jian; Sun, Qiang

    2013-05-28

    Metal-phthalocyanine porous sheets have uniformly dispersed metal sites in Pc framework, making absorption happen naturally. Here, we explore the effects of absorption of chlorine atoms on magnetism in transition metal embedded phthalocyanine (poly-TMPc) sheets with TM = Cr, Mn, and Fe. We show that when one Cl is absorbed on the TM, the strong square planar crystal field becomes weak in a square pyramidal configuration and the TM is in the +3 oxidized state, resulting in the magnetic moment of 3, 4, and 5 μB for Cr, Mn, and Fe, respectively, with weak antiferromagnetic couplings. When another Cl is introduced to the TM on the other side, it extracts one electron from the Pc framework making the substrate p-doped. The magnetic coupling is antiferromagnetic for poly-CrPc-2Cl and the poly-FePc-2Cl, while it becomes ferromagnetic for poly-MnPc-2Cl, suggesting that absorption can effectively modulate the bonding environment and tune the magnetic properties of the systems, and the controlled absorption can be used to tailor materials.