Relevant bibliographies by topics / Copper phthalocyanine

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Copper phthalocyanine'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 April 2022

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Journal articles on the topic "Copper phthalocyanine"

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Kim, Dong Hyun, Young Goo Kang, and Young Jin Kang. "Volatile Organic Compounds(VOCs) Sensing Properties of Thin Films Based on Copper phthalocyanine and Dilithium phthalocyanine Compounds." Journal of the Korean Society of Safety 28, no. 2 (April 30, 2013): 37–41. http://dx.doi.org/10.14346/jkosos.2013.28.2.037.

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Kutureva, Valentina, Natascha Baziakina, Ksenia Maximova, Valentina Morozova, Günter Schnurpfeil, Dieter Wöhrle, and Olga Suvorova. "Synthesis of new side-chain phthalocyanine methacrylate monomers for ophthalmosurgery in ophthalmology." Journal of Porphyrins and Phthalocyanines 12, no. 07 (July 2008): 832–38. http://dx.doi.org/10.1142/s1088424608000212.

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Convenient synthesis of new methacryloyloxy-substituted phthalocyanines for polymerization reactions, i.e. copper(II) 2,9,16,23-tetra(methacryloxyethoxycarbonyl)phthalocyanine and copper 2,9,16-tris(tert-butyl)-23-(methacryloxyethoxycarbonyl)phthalocyanine, consisting of just a few steps, has been developed. The copolymerization with a dimethacrylate derivative was investigated. The substituted phthalocyanines are interesting materials for ophthalmosurgery in ophthalmology (contact vision correction of eye lenses).
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MATHER, ROBERT R. "The Effect of Crystal Properties on the Manufacture and Application Performance of Copper Phthalocyanine Pigments." Journal of Porphyrins and Phthalocyanines 03, no. 07 (October 1999): 643–46. http://dx.doi.org/10.1002/(sici)1099-1409(199908/10)3:6/7<643::aid-jpp187>3.0.co;2-v.

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Copper phthalocyanines are commercially important organic pigments for blue shades of colour. They are dispersed by mechanical means as tiny molecular crystals (of dimensions 0.02—0.5 μm) into a wide range of commercial media to form products such as printing inks, paints and coloured plastics. Many important technological properties of copper phthalocyanine pigments, including colour strength and dispersion performance, depend on the physical properties of their crystals, notably crystal lattice type, crystal size and crystal shape. The roles which these crystal properties play in determining a copper phthalocyanine pigment's technological performance are briefly reviewed. The reduction of crystal aggregation during the manufacture of a copper phthalocyanine pigment and the control of flocculation in an application medium are also highlighted.
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SEMYANNIKOV, P. P., T. V. BASOVA, V. M. GRANKIN, and I. K. IGUMENOV. "Vapour pressure of some phthalocyanines." Journal of Porphyrins and Phthalocyanines 04, no. 03 (April 2000): 271–77. http://dx.doi.org/10.1002/(sici)1099-1409(200004/05)4:3<271::aid-jpp205>3.0.co;2-4.

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Mass spectrometric studies of the composition of the gaseous phase under solid compounds of free phthalocyanine ( H 2 Pc ) and its complexes with aluminium ( AlClPc , AlFPc , ( AlPc )2 O ) and copper ( CuPc ) were performed in the temperature range up to 700 °C. It has been shown that the phthalocyanines sublime in the form of monomers, excluding one aluminium complex. All phthalocyanines under investigation sublime without thermal decomposition until 700 °C. The vapour pressure of these phthalocyanines was determined as a function of temperature by the Knudsen effusion method, in which the rate of effusion of the equilibrium vapour through a small orifice was measured. The thermodynamic parameters of the sublimation process for phthalocyanies were calculated.
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Dixon, Dabney W., Anila F. Gill, and Brian R. Sook. "Characterization of sulfonated phthalocyanines by mass spectrometry and capillary electrophoresis." Journal of Porphyrins and Phthalocyanines 08, no. 11 (November 2004): 1300–1310. http://dx.doi.org/10.1142/s1088424604000672.

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We report the characterization of sulfonated phthalocyanines using capillary electrophoresis and mass spectrometry. Derivatives investigated included the copper, cobalt, zinc and metal-free sulfonated phthalocyanines. In general, sulfonated phthalocyanines were found as aggregates in capillary electrophoresis separations, even at low concentration. Separations were much better at pH 9.0 than at pH 2.5. The addition of β-cyclodextrin did not alter the electropherograms significantly. The electropherograms of commercially available copper phthalocyanine-3,4',4″,4‴-tetrasulfonic acid and 4,4',4″,4‴-tetrasulfonic acid were very different, consistent with the latter compound having a structure that is not fully sulfonated. Matrix-assisted laser desorption/ionization (MALDI) and electrospray ionization (ESI) were used to characterize the sulfonated phthalocyanines. In general, MALDI gave better results than ESI. Mass spectral evidence was obtained for a pentasulfonated species of both the metal-free phthalocyanine and zinc phthalocyanine when these species were made by sulfonation of the metal-free phthalocyanine (followed by zinc insertion in the latter case). Sulfonated tetraphenylporphyrin derivatives were used as standards for mass spectrometry and to estimate the effect of net charge on the capillary electrophoresis migration time for sulfonated tetrapyrroles. Clean separation of the sulfonated tetraphenylporphyrin derivatives [5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin (TPPS4), 5,10,15-tris(4-sulfonatophenyl)-20-phenylporphyrin (TPPS3) and 5,10-bis(4-sulfonatophenyl)-15,20-diphenylporphyrin (TPPS2a)] was observed by capillary electrophoresis.
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Leznoff, Clifford C., Sebastian M. Marcuccio, Shafrira Greenberg, A. B. P. Lever, and Kenneth B. Tomer. "Metallophthalocyanine dimers incorporating five-atom covalent bridges." Canadian Journal of Chemistry 63, no. 3 (March 1, 1985): 623–31. http://dx.doi.org/10.1139/v85-102.

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Metal-free copper and cobalt(II) binuclear phthalocyanines, in which the two phthalocyanine nuclci are covalently linked through five-atom bridges, have been prepared and characterized. Some new metal-free, copper, cobalt(II), and zinc 2,9,16,23-tetraalkoxyphthalocyanines, some of which are extremely soluble in organic solvents, are described.
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Hoshino, Akitaka, Yoshiko Takenaka, and Hideki Miyaji. "Redetermination of the crystal structure of α-copper phthalocyanine grown on KCl." Acta Crystallographica Section B Structural Science 59, no. 3 (May 23, 2003): 393–403. http://dx.doi.org/10.1107/s010876810300942x.

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The crystal structure of a polymorph of copper phthalocyanine (CuPc) grown on a KCl substrate is redetermined by transmission electron diffraction. It has a triclinic unit cell containing one molecule; the crystal does not have a herringbone-type molecular arrangement, which is a common packing mode of planar phthalocyanines. The molecular packing is determined by the diffraction intensity with the aid of the calculation of molecular packing energy. One of the striking features of this polymorph is its stacking mode within a molecular column: the molecular stacking direction projected on a molecular plane is different by an angle of about 45° from that of the α-modifications of platinum phthalocyanine (PtPc) and metal-free phthalocyanine (H2Pc). A powder X-ray diffraction profile calculated for the polymorph agrees well with that of so-called α-CuPc and Rietveld analysis for α-CuPc indicates that the CuPc crystals grown on KCl are actually α-CuPc; hence, α-CuPc is not isostructural with either α-PtPc or α-H2Pc. On the basis of the present results and the reported crystal structures of the planar phthalocyanines that form molecular columns, the polymorphs of the phthalocyanines can be classified into four types distinguished by the molecular stacking mode within the column: α(×)-, α(+)-, β(×)- and β(+)-types.
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LEZNOFF, CLIFFORD C., ANNA M. D'ASCANIO, and S. ZEKI YILDIZ. "Phthalocyanine formation using metals in primary alcohols at room temperature." Journal of Porphyrins and Phthalocyanines 04, no. 01 (January 2000): 103–11. http://dx.doi.org/10.1002/(sici)1099-1409(200001/02)4:1<103::aid-jpp209>3.0.co;2-e.

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Lithium metal added to a solution of 4-neopentoxyphthalonitrile in 1-octanol or other long-chain primary alcohols at room temperature resulted in phthalocyanine formation at a reasonable rate in good yield, while preformed lithium 1-octanolate under the same conditions gave 2,9,16,23-tetraneopentoxyphthalocyanine, but in lower yield at a slower rate. The use of lower-molecular-weight alcohols slowly gave a phthalocyanine in lower yields. Reverse micelle formation when using long-chain alcohols is proposed as a possibility for enhanced phthalocyanine formation at room temperature. 2,9,16,23-Tetrasubstituted phthalocyanines and metallated phthalocyanines were prepared at room temperature from 4-neopentoxyphthalonitrile, 4-bis(4-methoxyphenyl)methoxyphthalonitrile, 4-[1-(4-ethoxy-3-methoxyphenyl)-1-phenyl]methoxyphthalonitrile and phthalonitrile using lithium 1-octanolate in 1-octanol or by the addition, to a solution of the phthalonitrile in ethanol, of calcium turnings or, to a solution of the phthalonitrile in methanol, of magnesium, zinc, iron or copper powder. The tetrasubstituted phthalocyanines produced exhibited a non-statistical distribution of regioisomers, indicating that electronic effects become important in room-temperature cyclotetramerization of phthalonitriles to phthalocyanines.
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GREGORY, PETER. "Industrial applications of phthalocyanines." Journal of Porphyrins and Phthalocyanines 04, no. 04 (June 2000): 432–37. http://dx.doi.org/10.1002/(sici)1099-1409(200006/07)4:4<432::aid-jpp254>3.0.co;2-n.

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Phthalocyanines are the second most important class of colorant, and copper phthalocyanine is the single largest-volume colorant sold. Traditional uses of phthalocyanine colorants are as blue and green pigments for automotive paints and printing inks and as blue/cyan dyes for textiles and paper. Phthalocyanines have also found extensive use in many of the modern high technologies, e.g. as cyan dyes for ink jet printing, in electrophotography as charge generation materials for laser printers and as colorants for cyan toners. In the visible region, phthalocyanines are limited to blue, cyan and green colours. However, their absorption may be extended into the near infrared and by suitable chemical engineering it is possible to fingerprint the 700-1000 nm region. The properties and effects of these infrared-absorbing phthalocyanines are diverse and cover many important hi-tech applications, including photodynamic therapy, optical data storage, reverse saturable absorbers and solar screens.
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Garip, Ebru Özkan, Mukaddes Özçeşmeci, Ilgın Nar, İbrahim Özçeşmeci, and Esin Hamuryudan. "Novel phthalocyanines containing azo chromophores; synthesis, characterization, photophysical, and electrochemical properties." Journal of Porphyrins and Phthalocyanines 22, no. 01n03 (January 2018): 198–206. http://dx.doi.org/10.1142/s1088424618500050.

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A series of novel metal-free and zinc (II), copper (II), cobalt (II), and manganese (III) phthalocyanine complexes bearing peripheral 2,6-dimethyl-4-(4-tert-butyl-phenylazo)phenoxy units have been synthesized. Novel phthalonitrile derivative required for the preparation of these phthalocyanine complexes was prepared by a base-catalyzed nucleophilic aromatic nitro displacement of 4-nitrophthalonitrile with 2,6-dimethyl-4-(4-tert-butyl-phenylazo)phenol. The structures of these new compounds were characterized by using elemental analyses, proton and carbon nuclear magnetic resonance, Fourier transform infrared spectroscopy, ultraviolet–visible spectroscopy and mass spectrometry. The photophysical properties of metal-free and zinc(II) phthalocyanines were studied in tetrahydrofuran. The electrochemical properties of the phthalocyanine complexes were investigated by cyclic and square wave voltammetry.
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Dissertations / Theses on the topic "Copper phthalocyanine"

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Topuz, Burcu Berna. "Synthesis And Characterization Of Copper Phthalocyanine Deposited Mica Titania Pigment." Master's thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/3/12611519/index.pdf.

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In the present work, anatase and rutile titanium dioxide (TiO2) coated lustrous mica pigments were prepared by heterogeneous nucleation method. Anatase-rutile phase transformation of the TiO2 on mica substrate was achieved by coating very thin layers of tin (IV) oxide on mica surfaces prior to TiO2 deposition. Muscovite mica, which was used in the experiments was sieved, pre-treated with sodium bicarbonate and decantated before coating process. The surface morphology of mica titania pigments and anatase-rutile phase transformation were investigated by SEM and XRD analyse, respectively. Also, microwave-assisted synthesis of copper phthalocyanine and tetracarboxamide copper phthalocyanine pigments were carried out with phthalic anhydride and trimellitic anhydride precursors, respectively. Molecular structures of these pigments were confirmed by FT-IR and UV-visible spectroscopy analyse. Furthermore, combination pigments were obtained by the process of deposition of copper phthalocyanine pigments on mica-titania pigment substrate in dimethyl formamide solvent. FT-IR analysis and XRD analyse were performed to observe the transformations in the crystal forms of copper phthalocyanines on the substrate. The surface morphologies of copper phthalocyanines on the mica titania pigments were investigated by SEM analysis. Varying amounts of copper phthalocyanines were deposited on the mica surfaces, and nitrogen elemental analysis was performed to determine the amount of copper phthalocyanines. The resulting pigments were incorporated into alkyd based resin to prepare paint samples. L*a*b* values, gloss property, and hardness of the paint samples were determined by color measuring device, gloss meter and hardness measuring device, respectively. The resulting combination pigments obtained in this study showed improved luster, hue, and color intensity. Furthermore, in literature it was reported that these pigments have very high bleed resistance. This can be attributed to large macromolecular structure of copper phthalocyanine on the surface of mica titania pigment that prevents bleeding of the pigment from the paint. Moreover, the paint samples obtained from combination pigments showed higher hardness with respect to the paint sample of the mica titania pigment.
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Marda, Sandeep Kumar. "PHOTOVOLTAIC CELLS BASED ON COPPER PHTHALOCYANINE AND CADMIUM SULFIDE HETEROJUNCTION." UKnowledge, 2008. http://uknowledge.uky.edu/gradschool_theses/557.

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This work focuses on the solar cell based on the heterostructure formed between Copper Phthalocyanine (CuPc) and Cadmium Sulfide (CdS). Two different fabrication techniques were used for depositing the organic and inorganic layers of CuPc and CdS layers respectively. CuPc was deposited by electrodeposition while CdS was deposited by chemical bath deposition. Hybrid CdS/CuPc thin films were obtained from CdS films grown on Glass/ITO by chemical bath deposition followed by electrodeposition of CuPc onto these films and annealing at 250˚C after the deposition of each layer. The maximum open circuit voltage (Voc) and the short circuit current density (Jsc) obtained for this heterojunction solar cell are 0.59v and 0.7mA/cm2 respectively and these are the highest values achieved in literature till date. The materials characteristics and electrical performances of the device were analyzed. The effect of increasing the thickness of CuPc and CdS on the short circuit current density and open circuit voltage were also investigated.
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Starke, Thomas. "Gas sensing applications of phthalocyanine thin films." Thesis, Nottingham Trent University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312313.

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Din, Salahud. "Copper phthalocyanine (CuPc) thin films and nanostructures : growth and device applications." Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/11058.

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The development and utilisation of phthalocyanine (Pc) materials for practical applications has been subject of intense research due to their desirable optical, electrical, and recently discovered magnetic properties. Typically, in crystalline organic materials the charge transport, light absorption and magnetisation are anisotropic and strongly depend on structure, morphology and molecular orientation. Hence, an understanding of growth mechanism and controlled fabrication of thin films and nanostructures is essential for tailoring properties desirable for specific applications. e.g., for OFETs, crystalline thin films or one-dimensional nanostructures. Recently, vast advancement has been made in developing functional organic films including sublimation in (ultra) high vacuum using organic molecular beam deposition (OMBD). This environment can provide the essential material purity and structural reproducibility required in future high performance optoelectronic device applications, but is unfortunately costly. In this thesis, we introduce a lesser-known technique, organic vapour phase deposition (OVPD), operating at lower cost but still maintaining high purity. The morphology, crystallinity, spectroscopic characteristics and structure of copper phthalocyanine (CuPc) thin films and nanostructures have been investigated and their dependence on deposition conditions, i.e., substrate temperature and substrate type has been studied. We compare films obtained by OMBD and OVPD and find different morphological and structural changes; the surface morphology changes from granular to larger nano-fibrous and nano-whiskers with increasing substrate temperatures. In OMBD, the structure in a small proportion of the film changes from α-CuPc to β-CuPc at a substrate temperature of 200 oC. In the case of OVPD films, extensive study of the influence of parameters such as deposition pressure, deposition time and source to substrate distance is performed and variation in film morphology, texture, structural composition and molecular orientation is observed. We find that by successive growth of films produced by OMBD and OVPD, the molecular orientation can be controlled by the first “seed” layer. With further processing and optimisation, it is hoped that this could be used to create interpenetrating networks of different organic materials and optimal molecular orientation. We also demonstrate the fabrication using OVPD of high density CuPc nanowires with typical diameters between 10 - 100 nm, high directionality, and exceptional aspect ratios. We show that these nanowires are of a new crystal phase, named eta-CuPc. Lastly, OFETs fabricated with OMBD and OVPD grown CuPc thin films and nanowires are characterised. The current on/off ratio, mobilities and threshold voltage for thin films produced by the two methods are comparable and similar to what has been reported in literature. In contrast, OFETs with CuPc nanowires show remarkable improvement in turn-on voltage, while mobilities also seem to improve dramatically, although this is difficult to quantify. The challenges in growing CuPc nanowires directly on FETs with precise control of position and directionality are reviewed. The key issues that need to be resolved for future applications of these one-dimensional nanostructures are identified and are subject of on-going research. To conclude, this work has made important contribution in the efforts to develop, improve and enhance the deposition methods for fabricating functional thin films and nanostructures of CuPc material for use in organic electronic devices.
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Chintakula, Goutam. "SCHOTTKY DIODES ON COPPER PHTHALOCYANINE NANOWIRE ARRAYS EMBEDDED IN POROUS ALUMINA TEMPLATES." UKnowledge, 2008. http://uknowledge.uky.edu/gradschool_theses/556.

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Vertically aligned nanowire arrays of copper phthalocyanine (CuPc) and CuPc-Al Schottky diodes, of controllable diameter and length were fabricated by cathodic electrodeposition of CuPc into anodized alumina (AAO) templates, followed by annealing at 300 ºC in Argon. AAO over Aluminum tape and that over ITO-glass were both used as starting templates for the device fabrication. Depending on the dimensions of the starting AAO template, diameters of CuPc nanowires ranged from 30 nm to 40 nm and the lengths ranged from 500 nm to 1 μm. The temperature dependence of the phase and the absorption spectrum of the nanowires are reported. The electrodeposited nanowires (as prepared) had the preferred crystallite orientation of the α-phase. ITO formed the ohmic contact and Schottky contacts were formed between CuPc and aluminum. Insertion of a thin layer of PEDOT:PSS between CuPc nanowires and the ITO electrode improved the contact and reduced the series resistance by an order of magnitude. Schottky diodes were characterized and analyzed at room temperature and at cryogenic temperatures.
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Willis, Michael J. "Structural and polymorphic considerations on the effects of copper phthalocyanine pigment on polypropylene." Cincinnati, Ohio University of Cincinnati, 2007. http://www.ohiolink.edu/etd/view.cgi?ucin1179176317.

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Thesis (M.S.)--University of Cincinnati, 2007.
Title from electronic thesis title page (viewed July 18, 2007). Includes abstract. Keywords: polypropylene; nucleation; spherulite; copper phthalocyanine; pigment Includes bibliographical references.
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WILLIS, MICHAEL J. "STRUCTURAL AND POLYMORPHIC CONSIDERATIONS ON THE EFFECTS OF COPPER PHTHALOCYANINE PIGMENT ON POLYPROPYLENE NUCLEATION." University of Cincinnati / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179176317.

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Miller, Nicholas A. II. "Role of oxygen and water absorption on charge transport in copper phthalocyanine thin films." Thesis, California State University, Long Beach, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10164121.

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Organic semiconductors have been studied thoroughly and are well understood, though the effects in which oxygen and humidity have on them are less well known. In this thesis we immerse copper phthalocyanine thin films deposited at two different substrate temperatures and with two different thicknesses to an environment with oxygen pressures from 10 mbar to 210 mbar and water vapor pressures from 5 mbar to 13 mbar. The conductivity of our thin films at atmospheric oxygen and water pressure ranged from as high as 6:7 × 10−4 S/m and as low as 9:6 × 10−5 S/m, about 7 orders of magnitude less than silicon and germanium. At the smallest oxygen doping, the conductivity ranged from as high as 4:9 × 10−5 S/m to as low as 1:1 × 10−5 S/m. We can conclude that the small grain samples are more easily doped by oxygen, the small grain samples have a larger sensitivity gain than the large grain samples, and the intrinsic conductivity increases as both grain size decreases and as film thickness decreases.

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Siegert, Benjamin [Verfasser], Milena [Akademischer Betreuer] Grifoni, and Jascha [Akademischer Betreuer] Repp. "STM transport through copper phthalocyanine on thin insulating films / Benjamin Siegert. Betreuer: Milena Grifoni ; Jascha Repp." Regensburg : Universitätsbibliothek Regensburg, 2015. http://d-nb.info/1080609784/34.

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Hassan, Aseel Kadhim. "Studies in electronic conduction processes in organic semiconducting thin films of copper phthalocyanine prepared by evaporation." Thesis, Keele University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306847.

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Books on the topic "Copper phthalocyanine"

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Final report: Synthesis of phthalocyanine doped sol-gel materials. [Washington, D.C: National Aeronautics and Space Administration, 1993.

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Book chapters on the topic "Copper phthalocyanine"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) phthalocyanine polymer." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4, 912–14. Berlin, Heidelberg: Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_357.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) tetraamine phthalocyanine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4, 910–11. Berlin, Heidelberg: Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_356.

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Manzano, C., W. H. Soe, and C. Joachim. "High Voltage STM Imaging of Single Copper Phthalocyanine." In Imaging and Manipulating Molecular Orbitals, 15–26. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-38809-5_2.

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Zhu, Huabiao, Yuhuan Yang, Yingquan Peng, Wenli Lv, Sunan Xu, Yi Wei, Lei Sun, Ying Wang, and Fangzhi Guo. "Bending Characteristics of Flexible Organic Phototransistors Based on Copper Phthalocyanine." In Lecture Notes in Electrical Engineering, 202–7. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-8595-7_26.

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Lippel, P. H., R. J. Wilson, M. D. Miller, Ch Wöll, and S. Chiang. "High-Resolution Imaging of Copper-Phthalocyanine by Scanning-Tunneling Microscopy." In Scanning Tunneling Microscopy, 184–87. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-011-1812-5_27.

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Mingqing, Wang, and Wang Xiaogong. "P3HT/TiO2 Bulk Heterojunction Solar Cell Sensitized by Copper Phthalocyanine." In Proceedings of ISES World Congress 2007 (Vol. I – Vol. V), 1303–7. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75997-3_263.

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Kulesza, M., J. Kozioł, and W. Wacłwek. "Electrical Resistivity and IR Behaviour of Metal-Free and Copper Phthalocyanine — Carbon Black Mixtures." In Springer Series in Solid-State Sciences, 331–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-82569-9_59.

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Rawat, S. S., Ashish Kumar, Sanjay Kumar Swami, R. Srivastava, S. P. Khanna, and C. K. Suman. "Investigation of Magneto-conductance Transition Effect in Copper Phthalocyanine Thin Films: Electrical Impedance Study." In Springer Proceedings in Physics, 253–61. Singapore: Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-7691-8_25.

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Karimov, Khasan, Khakim Akhmedov, Mohammad Mahroof-Tahir, Rizwan M. Gul, and Abduakhad Ashurov. "Influence of Centrifugation on the Conductivity of Poly-N-Epoxypropylcarbazole — Copper Phthalocyanine Films Deposited from Solution." In Processing by Centrifugation, 93–98. Boston, MA: Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-0687-4_12.

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Mahato, Ajay Kumar, Deepak Bharti, Vivek Raghuwanshi, Ishan Varun, and Shree Prakash Tiwari. "Comprehensive Analysis of α- and β-form of Copper (II) Phthalocyanine for Organic Field-Effect Transistors." In Lecture Notes in Electrical Engineering, 503–11. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-3767-4_49.

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Conference papers on the topic "Copper phthalocyanine"

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Luo, Li-hao, Yu Fang, Xiang-yong Chu, Xing-zhi Wu, Junyi Yang, and Ying-lin Song. "Optical nonlinearity measurements of copper phthalocyanine film." In ISPDI 2013 - Fifth International Symposium on Photoelectronic Detection and Imaging, edited by Andreas Tünnermann, Zejin Liu, Pu Wang, and Chun Tang. SPIE, 2013. http://dx.doi.org/10.1117/12.2034318.

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Kwak, T. H., H. S. Kang, K. Kim, M. Y. Cho, J. W. Lee, and J. Joo. "Copper-phthalocyanine based organic thin film transistor." In 2006 IEEE Nanotechnology Materials and Devices Conference. IEEE, 2006. http://dx.doi.org/10.1109/nmdc.2006.4388937.

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Nair, Divya K., and K. Shreekrishna Kumar. "Development of gamma radiation dosimeter using copper phthalocyanine & zinc phthalocyanine based OFET." In 2017 IEEE International Conference on Circuits and Systems (ICCS). IEEE, 2017. http://dx.doi.org/10.1109/iccs1.2017.8326036.

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Gomes, Demetrius Saraiva, and Ana Neilde Rodrigues da Silva. "Electrospun nanofibers with copper phthalocyanine for detecting ammonia." In 2014 IEEE 9th Ibero-American Congress on Sensors (IBERSENSOR). IEEE, 2014. http://dx.doi.org/10.1109/ibersensor.2014.6995511.

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Liu, X., Y. Wang, M. Zhu, Y. Zhang, and Z. Wang. "Photocurrent characteristics of organic dye copper phthalocyanine transistors." In Proceedings of the 3RD International Conference of Electronic Engineering and Information Science (ICEEIS 2016). Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2016. http://dx.doi.org/10.1201/9781315265278-2.

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Zhang, Yu, Weimin Shi, Yuying Guo, Linjun Wang, and Guangpu Wei. "Investigation of copper phthalocyanine based Schottky solar cells." In Sixth International Conference on Thin Film Physics and Applications. SPIE, 2008. http://dx.doi.org/10.1117/12.792369.

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Singh, Vijay P., Suresh Rajaputra, Goutam Chintakula, Gayatri Sagi, and Sovannary Phok. "Schottky diode solar cells based on copper phthalocyanine nanowires." In 2008 33rd IEEE Photovolatic Specialists Conference (PVSC). IEEE, 2008. http://dx.doi.org/10.1109/pvsc.2008.4922492.

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Zhen, Lijuan, Liwei Shang, Ming Liu, and Ge Liu. "Copper phthalocyanine thin-film transistors with polyimide as dielectric." In 2007 IEEE Conference on Electron Devices and Solid-State Circuits. IEEE, 2007. http://dx.doi.org/10.1109/edssc.2007.4450314.

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Yoo, Hyung Keun, Youngwoon Yoon, Hanju Lee, Kiejin Lee, Chul Kang, Chul-Sik Kee, and Joong Wook Lee. "Angle-dependent carrier injection in copper phthalocyanine thin films." In Nano-Bio Sensing, Imaging and Spectroscopy, edited by Shin Won Kang, Seung-Han Park, Luke P. Lee, Ki-Bong Song, and Yo Han Choi. SPIE, 2013. http://dx.doi.org/10.1117/12.2018560.

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Hayatsu, Hikoya, Sanae Mimaki, Nao Ishizaki, Keiji Wakabayashi, and Chitose Sugiyama. "Copper phthalocyanine-chitin, an adsorbent for carcinogen–nucleotide adducts." In XIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199902175.

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