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Journal articles on the topic 'Organic thin films'

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Published: 4 June 2021
Last updated: 15 June 2025

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1

Sugi, Michio. "Organic Thin Films." IEEJ Transactions on Fundamentals and Materials 113, no. 11 (1993): 728–35. http://dx.doi.org/10.1541/ieejfms1990.113.11_728.

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2

SUGI, Michio. "Organic thin films." Hyomen Kagaku 10, no. 10 (1989): 804–10. http://dx.doi.org/10.1380/jsssj.10.804.

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3

Whitten, David G., Tisato Kajiyama, and Toyoki Kunitake. "Organic Thin Films: An Overview." MRS Bulletin 20, no. 6 (1995): 18–19. http://dx.doi.org/10.1557/s0883769400036927.

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The six articles comprising this issue of the MRS Bulletin deal with ultrathin films formed from organic molecules by a variety of techniques. In each case the component molecule forming the film is a relatively simple, single molecule which may or may not have important self-organizing properties that facilitate the formation of a film or related ordered molecular assembly. Taken together, the series of articles offer a concise look at the remarkable diversity and complexity of molecular thin films in terms of preparation and their properties.
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4

Gupta, Shiv K., Purushottam Jha, Ajay Singh, Mohamed M. Chehimi, and Dinesh K. Aswal. "Flexible organic semiconductor thin films." Journal of Materials Chemistry C 3, no. 33 (2015): 8468–79. http://dx.doi.org/10.1039/c5tc00901d.

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5

Taniguchi, Yoshio. "Organic Thin Films for Electronics." Kobunshi 36, no. 4 (1987): 264. http://dx.doi.org/10.1295/kobunshi.36.264.

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6

Tkachenko, Nikolai V., Vladimir Chukharev, Petra Kaplas, et al. "Photoconductivity of thin organic films." Applied Surface Science 256, no. 12 (2010): 3900–3905. http://dx.doi.org/10.1016/j.apsusc.2010.01.047.

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7

Andrade, J. D. "Thin organic films of proteins." Thin Solid Films 152, no. 1-2 (1987): 335–43. http://dx.doi.org/10.1016/0040-6090(87)90425-1.

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8

Andreev, A., R. Resel, D. M. Smilgies, et al. "Oriented organic semiconductor thin films." Synthetic Metals 138, no. 1-2 (2003): 59–63. http://dx.doi.org/10.1016/s0379-6779(03)00025-0.

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9

Sanche, L. "Transmission through Organic Thin Films." Physical Review Letters 75, no. 15 (1995): 2904. http://dx.doi.org/10.1103/physrevlett.75.2904.

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10

Dörfler, H. D. "Order in Thin Organic Films." Zeitschrift für Physikalische Chemie 189, Part_2 (1995): 276. http://dx.doi.org/10.1524/zpch.1995.189.part_2.276.

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11

Mai, Manfang, Shanming Ke, Peng Lin, and Xierong Zeng. "Ferroelectric Polymer Thin Films for Organic Electronics." Journal of Nanomaterials 2015 (2015): 1–14. http://dx.doi.org/10.1155/2015/812538.

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The considerable investigations of ferroelectric polymer thin films have explored new functional devices for flexible electronics industry. Polyvinylidene fluoride (PVDF) and its copolymer with trifluoroethylene (TrFE) are the most commonly used polymer ferroelectric due to their well-defined ferroelectric properties and ease of fabrication into thin films. In this study, we review the recent advances of thin ferroelectric polymer films for organic electronic applications. Initially the properties of ferroelectric polymer and fabrication methods of thin films are briefly described. Then the theoretical polarization switching models for ferroelectric polymer films are summarized and the switching mechanisms are discussed. Lastly the emerging ferroelectric devices based on P(VDF-TrFE) films are addressed. Conclusions are drawn regarding future work on materials and devices.
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12

MURATA, Masahiko, Toshiro DOI, Syuhei KUROKAWA, et al. "3371 Study on Formation of Films by a Spray Deposition Method for the Organic Thin Film Solar Cells." Proceedings of International Conference on Leading Edge Manufacturing in 21st century : LEM21 2011.6 (2011): _3371–1_—_3371–4_. http://dx.doi.org/10.1299/jsmelem.2011.6._3371-1_.

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13

Zhao, Cindy X., Steven Xiao, and Gu Xu. "Density of organic thin films in organic photovoltaics." Journal of Applied Physics 118, no. 4 (2015): 044510. http://dx.doi.org/10.1063/1.4927752.

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14

Miyazaki, Yuzuru. "Miyazaki Laboratory research in: thermoelectric materials, organic thin films, photovoltaic thin films." Impact 2018, no. 5 (2018): 19–21. http://dx.doi.org/10.21820/23987073.2018.5.19.

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15

NOMAKI, TATSUO, AKIKO YAMANAKA, and KATSUYUKI NAITO. "THERMAL ANALYSIS OF ORGANIC THIN FILMS." Analytical Sciences 7, Supple (1991): 1287–88. http://dx.doi.org/10.2116/analsci.7.supple_1287.

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16

KUROSAKI, Kazuo. "Surface analysis of organic thin films." Journal of the Metal Finishing Society of Japan 36, no. 12 (1985): 520–27. http://dx.doi.org/10.4139/sfj1950.36.520.

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17

Bartholomeusz, Brian J., and Mool C. Gupta. "Laser marking of thin organic films." Applied Optics 31, no. 23 (1992): 4829. http://dx.doi.org/10.1364/ao.31.004829.

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18

Tang, C. W., S. A. VanSlyke, and C. H. Chen. "Electroluminescence of doped organic thin films." Journal of Applied Physics 65, no. 9 (1989): 3610–16. http://dx.doi.org/10.1063/1.343409.

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19

Nicole, Lionel, Cédric Boissière, David Grosso, Alida Quach, and Clément Sanchez. "Mesostructured hybrid organic–inorganic thin films." Journal of Materials Chemistry 15, no. 35-36 (2005): 3598. http://dx.doi.org/10.1039/b506072a.

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20

PALFFY-MUHORAY, P., and K. D. SINGER. "DISPLAYS BASED ON ORGANIC THIN FILMS." Optics and Photonics News 6, no. 9 (1995): 16. http://dx.doi.org/10.1364/opn.6.9.000016.

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21

Manson, J. R., and J. G. Skofronick. "Multiphonon effects in thin organic films." Physical Review B 47, no. 19 (1993): 12890–94. http://dx.doi.org/10.1103/physrevb.47.12890.

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22

Zhou, Y. C., Y. Wu, L. L. Ma, J. Zhou, X. M. Ding, and X. Y. Hou. "Exciton migration in organic thin films." Journal of Applied Physics 100, no. 2 (2006): 023712. http://dx.doi.org/10.1063/1.2215196.

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23

Okui, Norimasa. "Ultra Thin Organic and Polymer Films." International Journal of Polymeric Materials 15, no. 3-4 (1991): 249–52. http://dx.doi.org/10.1080/00914039108041091.

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24

Ehara, Toshihiro, Hidekazu Hirose, Hiroyuki Kobayashi, and Masahiro Kotani. "Molecular alignment in organic thin films." Synthetic Metals 109, no. 1-3 (2000): 43–46. http://dx.doi.org/10.1016/s0379-6779(99)00196-4.

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25

Fraxedas, J., J. Caro, J. Santiso, A. Figueras, P. Gorostiza, and F. Sanz. "Surface morphology of organic thin films." Applied Surface Science 144-145 (April 1999): 623–26. http://dx.doi.org/10.1016/s0169-4332(98)00878-2.

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26

Ebert, B., Th Hanke, I. Boem, and W. Vollmann. "Investigation of conducting organic thin films." Synthetic Metals 42, no. 1-2 (1991): 1957–60. http://dx.doi.org/10.1016/0379-6779(91)91992-j.

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27

Norian, K. H., and U. Rieck. "Metal-organic-compound-polymer thin films." Thin Solid Films 182, no. 1-2 (1989): L21—L24. http://dx.doi.org/10.1016/0040-6090(89)90275-7.

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28

Al-Mohamad, A., C. W. Smith, I. S. Al-Saffar, and M. A. Slifkin. "Thin organic films for electronics applications." Thin Solid Films 189, no. 1 (1990): 175–81. http://dx.doi.org/10.1016/0040-6090(90)90037-e.

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29

Fraxedas, J. "Thin films of molecular organic materials." Journal of Physics: Condensed Matter 20, no. 18 (2008): 180301. http://dx.doi.org/10.1088/0953-8984/20/18/180301.

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30

KAWABATA, Yasujiro. "Electrical properties of organic thin films." Hyomen Kagaku 7, no. 6 (1986): 454–63. http://dx.doi.org/10.1380/jsssj.7.454.

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31

Zacher, Denise, Osama Shekhah, Christof Wöll, and Roland A. Fischer. "Thin films of metal–organic frameworks." Chemical Society Reviews 38, no. 5 (2009): 1418. http://dx.doi.org/10.1039/b805038b.

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32

Petty, M. C. "Gas sensing using thin organic films." Biosensors and Bioelectronics 10, no. 1-2 (1995): 129–34. http://dx.doi.org/10.1016/0956-5663(95)96800-e.

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33

Fraxedas, J. "Perspectives on Thin Molecular Organic Films." Advanced Materials 14, no. 22 (2002): 1603–14. http://dx.doi.org/10.1002/1521-4095(20021118)14:22<1603::aid-adma1603>3.0.co;2-5.

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34

Whitesell, James K., Hye Kyung Chang, and Christopher S. Whitesell. "Enzymatic Grooming of Organic Thin Films." Angewandte Chemie International Edition in English 33, no. 8 (1994): 871–73. http://dx.doi.org/10.1002/anie.199408711.

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35

Rahmati, Zahra, Ruhollah Khajavian, and Masoud Mirzaei. "Anisotropy in metal–organic framework thin films." Inorganic Chemistry Frontiers 8, no. 14 (2021): 3581–86. http://dx.doi.org/10.1039/d1qi00300c.

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36

XUE, Z. Q., H. J. GAO, W. M. LIU, Y. W. LIU, Q. D. WU, and S. J. PANG. "STUDY OF METALLIC CLUSTERS IN ORGANIC THIN FILMS." Surface Review and Letters 03, no. 01 (1996): 1029–32. http://dx.doi.org/10.1142/s0218625x96001844.

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The polyethylene (PE) and the metallic materials are deposited alternatively on substrates in the chamber of the ICB-TOFMS deposition system. The metallic-cluster-polyethylene thin films are formed. The film thickness is about 30 nm. The structures of these samples including Au-PE, Ag-PE, In-PE, and Sn-PE thin films are studied. These special thin films with suspension metal clusters display many special properties.
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37

Fan Zhang, Fan Zhang, Cong Wang Cong Wang, Kai Yin Kai Yin, et al. "Investigation on optical and photoluminescence properties of organic semiconductor Al-Alq3 thin films for organic light-emitting diodes application." Chinese Optics Letters 15, no. 11 (2017): 111602. http://dx.doi.org/10.3788/col201715.111602.

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38

Yang, Fan, Jun Li, Yin Long, et al. "Wafer-scale heterostructured piezoelectric bio-organic thin films." Science 373, no. 6552 (2021): 337–42. http://dx.doi.org/10.1126/science.abf2155.

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Piezoelectric biomaterials are intrinsically suitable for coupling mechanical and electrical energy in biological systems to achieve in vivo real-time sensing, actuation, and electricity generation. However, the inability to synthesize and align the piezoelectric phase at a large scale remains a roadblock toward practical applications. We present a wafer-scale approach to creating piezoelectric biomaterial thin films based on γ-glycine crystals. The thin film has a sandwich structure, where a crystalline glycine layer self-assembles and automatically aligns between two polyvinyl alcohol (PVA) thin films. The heterostructured glycine-PVA films exhibit piezoelectric coefficients of 5.3 picocoulombs per newton or 157.5 × 10−3 volt meters per newton and nearly an order of magnitude enhancement of the mechanical flexibility compared with pure glycine crystals. With its natural compatibility and degradability in physiological environments, glycine-PVA films may enable the development of transient implantable electromechanical devices.
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39

Chen, Hai Nian, Ai Miao Qin, Lei Liao, Ping Tang, and Qi Pang. "Electrodeposited Crack-Free CdS Thin Films Using Organic Solvents." Advanced Materials Research 194-196 (February 2011): 2404–8. http://dx.doi.org/10.4028/www.scientific.net/amr.194-196.2404.

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Crack-free CdS thin films have been electrodeposited on conductive glass substrate by CdCl2 and S powder in dimethylformamide (DMF) and mixed organic solvents with appropriate volume ratio at temperatures lower than 100°C. The effects of solvents on the cracks and the photovoltaic property and catalytic property of CdS thin film are investigated. The results show that the crack-free CdS thin films have higher photoluminescence (PL) emission intensity and better photoelectrichemistry and photocatalytic activities for degradation organic dyes of Fuchsin acid, phenol red and crystal violet than thin films with cracks.
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40

Murase, Seiichiro, Aki Makiyama, Tsuyoshi Tominaga, Akira Kohama, and Tetsuo Oka. "Photophysical Studies on Organic Thin Solid Films." Journal of Photopolymer Science and Technology 14, no. 2 (2001): 313–16. http://dx.doi.org/10.2494/photopolymer.14.313.

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41

Jelinek, M., T. Kocourek, J. Remsa, R. Cristescu, I. N. Mihailescu, and D. B. Chrisey. "MAPLE applications in studying organic thin films." Laser Physics 17, no. 2 (2007): 66–70. http://dx.doi.org/10.1134/s1054660x0702003x.

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42

Forrest, S. R., M. L. Kaplan, and P. H. Schmidt. "Organic Thin Films for Semiconductor Wafer Diagnostics." Annual Review of Materials Science 17, no. 1 (1987): 189–217. http://dx.doi.org/10.1146/annurev.ms.17.080187.001201.

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43

HIGAKI, KENJIN, CHIAKI NAGAI, OSAMU MURATA, and HAYAMI ITOH. "Organic thin films formation by laser ablation." Journal of Photopolymer Science and Technology 6, no. 3 (1993): 429–32. http://dx.doi.org/10.2494/photopolymer.6.429.

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44

Wright, John D. "Discussion session summary: MD2, Organic Thin Films." Journal of Materials Chemistry 10, no. 1 (2000): 195–205. http://dx.doi.org/10.1039/a908793a.

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45

Gao, Hongjun, Geoffrey S. Canright, Shijin Pang, Ilya M. Sandler, Zengquan Xue, and Zhenyu Zhang. "Unique Dendritic Patterns in Organic Thin Films." Fractals 06, no. 04 (1998): 337–50. http://dx.doi.org/10.1142/s0218348x98000390.

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We present the formation of unique and striking dendritic "seahorse" patterns in the growth of fullerene-tetracyanoquinodimethane ( C 60-TCNQ) or pune TCNQ thin films. The films were fabricated by an ionized-cluster-beam deposition method. Energetic neutral and charged clusters were deposited on amorphous carbon substrates. Transmission electron microscopy reveals that the elemental pattern is a "seahorse" — that is, an S-shaped form, with "fins" on the outer edges of the curved arms forming the S. Such forms possess an approximate symmetry under rotations by π, but strongly break two-dimensional inversion symmetry. A novel formation mechanism is proposed, involving the aggregatio of neutral and charged clusters, such that some electrostatic charge is trapped on each growing island. This charge gives rise to a long-range field which biases the growth in a nontrivial way. The broken symmetry arises from the strong amplification of noise in the diffusive aggregation process by the effects of the electro-static field — that is, the symmetry breaking is spontaneous. This picture is tested by applying a transverse electric field during growth: for sufficiently strong fields, the S-shaped "seahorses" lose their curvature, while retaining the feature of having two main arms. These results demonstrate the importance of electrostatic effects in the growth process, and are consistent with the growth mechanism described here.
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46

Chattopadhyay, Basab, and Yves Geerts. "Substrate Induced Polymorphism in Organic Thin Films." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C728. http://dx.doi.org/10.1107/s2053273314092717.

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The presence of substrate induced polymorphic phases in thin films is an intriguing phenomenon with the physical and chemical factors responsible for its formation are not yet clearly understood. In particular, this is really crucial in the field of organic electronics, where the charge-transport properties are highly dependent on crystal packing, especially for organic field-effect transistors where charge transport occurs at the interface between the organic semiconductor and the dielectric. In pharmaceutical sector, thin film drug delivery is the new emerging alternative to traditional tablets and oral suspensions. The need to identify and control polymorphism induced by the substrate is thus very crucial. In this presentation, we report the structure and morphological changes associated with a substrate induced polymorphic phases in a discotic liquid crystal and a rod shaped DPP-thiophene-based molecule [1, 2]. The bulk compound and the thin films are characterized by a combination of various X-ray diffraction methods to investigate the structural properties. Atomic force microscopy and polarized optical microscopy are used to determine the thin film morphologies. This is the first experimental proof of presence of a substrate induced phase in discotic liquid crystal showcasing an unique example where the 2-D liquid crystalline phase converts to a 3-D crystal plastic phase due to nucleation caused by the solid substrate over a time scale of a month or longer. The presentation also highlights the importance of polymorphism in DPP-thiophene-based material and the specific organization that could arise from the interaction with the substrate depending on the growing conditions. Here the exact structural and the spectroscopic signatures of different polymorphic forms in bulk and in thin films could be identified. These are clearly factors to consider to induce the formation of a particular polymorph and to help to design deposition methodologies.
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47

WATANABE, Kazuya. "Ultrafast Spectral Diffusion in Organic Thin Films." Review of Laser Engineering 50, no. 1 (2022): 11. http://dx.doi.org/10.2184/lsj.50.1_11.

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48

Niemelä, J. P., A. J. Karttunen, and M. Karppinen. "Inorganic–organic superlattice thin films for thermoelectrics." Journal of Materials Chemistry C 3, no. 40 (2015): 10349–61. http://dx.doi.org/10.1039/c5tc01643f.

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Nanoscale layer-engineering using the combined atomic/molecular layer deposition (ALD/MLD) technique for the fabrication of oxide–organic thin-film superlattices is an attractive way to tailor the performance of thermoelectric materials as it potentially allows us to suppress thermal conductivity without significantly hindering the electrical transport properties.
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49

Tierney, Michael, and David Lubman. "Laser-Induced Photoconductivity in Thin Organic Films." Applied Spectroscopy 41, no. 5 (1987): 880–86. http://dx.doi.org/10.1366/0003702874448274.

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Photoconductivity in polynuclear aromatic hydrocarbons has been shown to be wavelength dependent and related to the electronic absorption spectrum. Photoconductivity is studied in several PNAHs with the use of light from a pulsed dye laser. The voltage dependence, light intensity dependence, and temperature dependence and the effect of ambient gases on the photocurrent are investigated in thin-film samples on a surface-type cell. The majority charge carriers are holes which flow across the surface of the sample. Photocurrents on the order of microamperes are observed. A preliminary investigation of the effect of temperature on the spectral dependence of the photocurrent shows that the peaks narrow when the sample is cooled to 80 K. This technique may prove useful as a method of obtaining sharp spectra of some organic thin films.
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50

Scholz, Sebastian, Cathrin Corten, Karsten Walzer, Dirk Kuckling, and Karl Leo. "Photochemical reactions in organic semiconductor thin films." Organic Electronics 8, no. 6 (2007): 709–17. http://dx.doi.org/10.1016/j.orgel.2007.06.002.

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