Academic literature on the topic '3-dodecylthiophene'

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Journal articles on the topic "3-dodecylthiophene"

1

Musselman, I. "Poly(3-dodecylthiophene) membranes for gas separations." Journal of Membrane Science 152, no. 1 (January 6, 1999): 1–18. http://dx.doi.org/10.1016/s0376-7388(98)00127-6.

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2

Qiao, Xiuying, Xianhong Wang, Xiaojiang Zhao, Zhishen Mo, and Hongfang Zhang. "Nonisothermal crystallization of poly(3-dodecylthiophene) and poly(3-octadecylthiophene)." Synthetic Metals 113, no. 1-2 (June 2000): 1–6. http://dx.doi.org/10.1016/s0379-6779(99)00131-9.

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3

Čı́k, G., F. Šeršeň, and L. Dlháň. "Diamagnetism of poly(3-dodecylthiophene) doped with FeCl3." Journal of Magnetism and Magnetic Materials 208, no. 1-2 (January 2000): 78–84. http://dx.doi.org/10.1016/s0304-8853(99)00574-0.

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4

Qiao, Xiuying, Xueshan Xiao, Xianhong Wang, Jian Yang, Zhaobin Qiu, Lijia An, Wenkui Wang, and Zhishen Mo. "External field induced crystallization of poly(3-dodecylthiophene)." European Polymer Journal 38, no. 6 (June 2002): 1183–90. http://dx.doi.org/10.1016/s0014-3057(01)00289-0.

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5

Lee, S. B., K. Yoshino, J. Y. Park, and Y. W. Park. "Extrinsic photoconductivity in poly(3-dodecylthiophene) sandwich cells." Physical Review B 61, no. 3 (January 15, 2000): 2151–58. http://dx.doi.org/10.1103/physrevb.61.2151.

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6

Rumbles, G., I. D. W. Samuel, L. Magnani, K. A. Murray, A. J. DeMello, B. Crystall, S. C. Moratti, B. M. Stone, A. B. Holmes, and R. H. Friend. "Chromism and luminescence in regioregular poly(3-dodecylthiophene)." Synthetic Metals 76, no. 1-3 (January 1996): 47–51. http://dx.doi.org/10.1016/0379-6779(95)03417-i.

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Jinwei, Wang, and M. P. Srinivasan. "Conductive composite films of polyimide and poly(3-dodecylthiophene)." Synthetic Metals 105, no. 1 (August 1999): 1–7. http://dx.doi.org/10.1016/s0379-6779(99)00069-7.

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8

Westerling, M., R. Österbacka, and H. Stubb. "Recombination of electronic excitations in regioregular poly(3-dodecylthiophene)." Thin Solid Films 403-404 (February 2002): 510–12. http://dx.doi.org/10.1016/s0040-6090(01)01579-6.

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Liu, S. L., and T. S. Chung. "Crystallization and melting behavior of regioregular poly(3-dodecylthiophene)." Polymer 41, no. 8 (April 2000): 2781–93. http://dx.doi.org/10.1016/s0032-3861(99)00490-5.

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Šeršeň, F., G. Čík, L. Szabo, and L. Dlháň. "Antiferromagnetism of poly(3-dodecylthiophene) irradiated by γ-beams." Journal of Radioanalytical and Nuclear Chemistry Letters 212, no. 1 (January 1996): 1–9. http://dx.doi.org/10.1007/bf02165445.

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Dissertations / Theses on the topic "3-dodecylthiophene"

1

Krajčovič, Jozef. "Studium thiofenových oligo-kopolymerů: syntéza a optoelektronické vlastnosti." Doctoral thesis, Vysoké učení technické v Brně. Fakulta chemická, 2010. http://www.nusl.cz/ntk/nusl-233316.

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Thesis presents synthesis and study of thiophene monomers, oligomers and polymers. The new series of thieno[3,4-b]pyrazine copolymers based on 3-dodecylthiophene and pyrazine monomers were prepared by oxidative polymerization with FeCl3. The effective synthetic method for preparation of 3-alkylthiophenes and thiophene oligomers was developed by optimizing of Kumada cross-couplig. The mentioned method could be realized for multikilos scale with possibility of transfer to pilot plant production. The second part of thesis focuses on synthesis and study of new thiophene compounds, which consist of both 2,3-diazo-1,3-butadiene bridge with two terminal chromophores and two thiophene units linked together via -position by pyrazine or hydrazine bridge. Finally, the new type of regular alternating copolymer consists of 2,2´:5´,2´´-terthiophene-5,5´-dicarboxylic acid (TEDA) and polyethyleneoxide (PEO) was prepared. Formation of polymer nano-subunits as separated phases in solid state was confirmed by TEM.
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Wang, Shin-guo, and 王信國. "The Crystallization of Side Chain Effect on the Performances of Poly(3-dodecylthiophene)/fullerene “Bulk Heterojunction” Solar Cells." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/33xzx3.

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Abstract:
碩士
國立中山大學
光電工程學系研究所
97
P3DDT (3-dodecylthiophene-2,5-diyl) and PCBM( [6,6]-phenyl C61-butyric acid methyl ester) were fabricated to the active layer of Bulk Heterojunction Organic Solar Cells .We obtained the device efficiency was 0.64 % by evaporating solvent at room temperature. We measured Thermal decomposition Temperature (Td) of P3DDT was 487℃. But operational temperature was over 90℃, it could affect the roughness of thin film and make efficiency to be 4×10-3(%). For results of experiments, we know that roughness changed by the crystallization of side chain and exciton dissociation modified by the morphology between P3DDT and PCBM. Thin film solar cell has a large effect on the formation of active layer, such as heat treatment, choices of solvents, composition ratio, and speed of spin coating. The efficiency of solar cell has been shown to be highly sensitive to the size, composition and crystallization of the formed domains. We studied two kinds of conjugated polythiophenes with the same main chain but different side chain. When the number of carbon atoms of alkyl side chains is more than 10, some orderly arrangements will occur for side chains between the layers. We tried to explain the crystallization caused by long alkyl side chains determined which intrinsic phenomena are the most evident for altering the PCE of solar cell. After recrystallization, the layered structures of P3DDT can be improved, but those orderly degrees of the arrangements with PCBM are further aggregated. The main point for low PEC and Jsc by heat treatment is the unfavorable and roughened morphology. Charge transfer only occurs at the boundary ,which is interfacial area between donor and acceptor materials, hence, the low Jsc could be caused by poor charge transfer between P3DDT and PCBM. The redistributed arrangement of P3DDT domains exclude PCBM from original space, and it makes PCBM to aggregate large particles, from nanophase to mesophase scales, which reduce mutual solubility to be the source of PCE and Jsc reduction.
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