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Journal articles on the topic 'Poly(3-hexylthiophene)'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 September 2023

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1

Guo, Yan, Lang Jiang, Xiaojing Ma, Wenping Hu, and Zhaohui Su. "Poly(3-hexylthiophene) monolayer nanowhiskers." Polymer Chemistry 4, no. 16 (2013): 4308. http://dx.doi.org/10.1039/c3py00728f.

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2

Bauer, Peter, Michael Sommer, Johann Thurn, Martti Pärs, Jürgen Köhler, and Mukundan Thelakkat. "A photoswitchable poly(3-hexylthiophene)." Chemical Communications 49, no. 41 (2013): 4637. http://dx.doi.org/10.1039/c3cc41765d.

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3

Hernández-Martínez, D., C. Martínez-Alonso, M. M. Castillo-Ortega, M. C. Arenas-Arrocena, and M. E. Nicho. "Preparation and characterization of electrospun fibers containing poly(3-hexylthiophene) and poly(3-hexylthiophene)/CdS." Synthetic Metals 209 (November 2015): 496–501. http://dx.doi.org/10.1016/j.synthmet.2015.09.001.

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4

Sansomboon, A., T. Jungwon, P. Pasitsuparoad, K. Subannajui, and T. Osotchan. "Fabrication and I-V Characterization with Monochromatic Light of Multilayer Poly(3-hexylthiophene)-CNT/C60 Thin Films on ITO Glass Substrate." Advanced Materials Research 770 (September 2013): 315–18. http://dx.doi.org/10.4028/www.scientific.net/amr.770.315.

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Multilayer poly (3-hexylthiophene)-CNT/C60 thin films on ITO glass substrate was fabricated regarding to the function of each layer. Poly (3-hexylthiophene) (P3HT) is used as a donor layer and fullerene (C60) is used as an acceptor layer of the device. The carbon-nanotube (CNT) is homogeneously mixed in the donor layer to increase charge transportability. The structures of poly (3-hexylthiophene), poly (3-hexylthiophene)-CNT were fabricated in comparison of poly (3-hexylthiophene)-CNT/C60 thin films. The P3HT-CNT bulk heterojunction was deposited on ITO glass substrate by spin coating technique and then the C60 thin film was deposited on the P3HT by thermal evaporating technique. The I-V characteristic of ITO/P3HT-CNT/Al and ITO/P3HT-CNT/C60/Al were investigated in the monochromatic light. The result showed that the ITO/P3HT-CNT/Al structures respond with red and green light, and the ITO/P3HT-CNT/C60/Al structure responds with blue light. The UV absorption was measured and the result was consistence with the I-V characterization.

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5

Melis, Claudio, Luciano Colombo, and Alessandro Mattoni. "Self-Assembling of Poly(3-hexylthiophene)." Journal of Physical Chemistry C 115, no. 2 (December 21, 2010): 576–81. http://dx.doi.org/10.1021/jp109175b.

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6

Heffner, Glenn W., and Dale S. Pearson. "Molecular characterization of poly(3-hexylthiophene)." Macromolecules 24, no. 23 (November 1991): 6295–99. http://dx.doi.org/10.1021/ma00023a035.

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7

de Paula, F. R., L. Walmsley, E. C. Pereira, and A. J. A. de Oliveira. "Magnetic properties of poly(3-hexylthiophene)." Journal of Magnetism and Magnetic Materials 320, no. 14 (July 2008): e193-e195. http://dx.doi.org/10.1016/j.jmmm.2008.02.045.

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8

Gustafsson, G., O. Inganäs, M. Sundberg, and C. Svensson. "Rectifying metal/poly(3-hexylthiophene) contacts." Synthetic Metals 41, no. 1-2 (April 1991): 499–502. http://dx.doi.org/10.1016/0379-6779(91)91117-s.

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9

Hamaguchi, Maki, Hidetaka Nambu, and Katsumi Yoshino. "Electrogenerated Chemiluminescence from Poly(3-hexylthiophene)." Japanese Journal of Applied Physics 36, Part 2, No. 2A (February 1, 1997): L124—L126. http://dx.doi.org/10.1143/jjap.36.l124.

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10

Kuo, C. S., F. G. Wakim, S. K. Sengupta, and S. K. Tripathy. "Schottky diodes using poly(3‐hexylthiophene)." Journal of Applied Physics 74, no. 4 (August 15, 1993): 2957–58. http://dx.doi.org/10.1063/1.355319.

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11

Gao, Lei, Yi-ming Tian, Wei Hou, Wei-Qing Yan, and Gao-yu Zhong. "Piezoresistance of Poly(3-Hexylthiophene) Film." Advances in Polymer Technology 37, no. 3 (May 4, 2016): 662–67. http://dx.doi.org/10.1002/adv.21707.

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12

Roesing, Miranda, Jason Howell, and David Boucher. "Solubility characteristics of poly(3-hexylthiophene)." Journal of Polymer Science Part B: Polymer Physics 55, no. 14 (May 2, 2017): 1075–87. http://dx.doi.org/10.1002/polb.24364.

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13

Lim, Herman, Chi-Yang Chao, and Wei-Fang Su. "Modulating Crystallinity of Poly(3-hexylthiophene) via Microphase Separation of Poly(3-hexylthiophene)–Polyisoprene Block Copolymers." Macromolecules 48, no. 10 (May 12, 2015): 3269–81. http://dx.doi.org/10.1021/ma502417w.

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14

Cui, Huina, Xiubao Yang, Juan Peng, and Feng Qiu. "Controlling the morphology and crystallization of a thiophene-based all-conjugated diblock copolymer by solvent blending." Soft Matter 13, no. 31 (2017): 5261–68. http://dx.doi.org/10.1039/c7sm01126a.

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We report the crystallization and microphase separation behavior of an all-conjugated poly(3-hexylthiophene)-b-poly[3-(6-hydroxy)hexylthiophene] (P3HT-b-P3HHT) block copolymer in mixed solvents and demonstrate how the conformations of P3HT and P3HHT chains influence the photophysical properties of the copolymer.

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15

Minkler, Michael J., Jihyuk Kim, Katherine E. Lawson, Ashraf Ali, Rong Zhao, Andrew J. Adamczyk, and Bryan S. Beckingham. "Solution processible statistical poly(3-methoxythiophene)-co-poly(3-hexylthiophene) copolymer." Materials Letters 256 (December 2019): 126563. http://dx.doi.org/10.1016/j.matlet.2019.126563.

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16

Higashihara, Tomoya, Seijiro Fukuta, Tomoyuki Koganezawa, and Keisuke Chino. "Morphological Study of Blend Thin Films of Poly(3-hexylthiophene)-block-polyisobutylene-block-poly(3-hexylthiophene):Poly(3-hexylthiophene) and Their Application to Photovoltaics." Journal of Photopolymer Science and Technology 32, no. 5 (June 24, 2019): 741–46. http://dx.doi.org/10.2494/photopolymer.32.741.

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17

Marchant, S., W. R. E. Brakenbury, J. Horder, and P. J. S. Foot. "Ellipsometric analysis of poly(3-hexylthiophene) surfaces." Journal of Materials Science Letters 12, no. 15 (January 1993): 1154–55. http://dx.doi.org/10.1007/bf00274482.

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18

Scarpa, Giuseppe, Anna-Lena Idzko, Anandi Yadav, and Stefan Thalhammer. "Organic ISFET Based on Poly (3-hexylthiophene)." Sensors 10, no. 3 (March 19, 2010): 2262–73. http://dx.doi.org/10.3390/s100302262.

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19

Roehling, John D., Ilke Arslan, and Adam J. Moulé. "Controlling microstructure in poly(3-hexylthiophene) nanofibers." J. Mater. Chem. 22, no. 6 (2012): 2498–506. http://dx.doi.org/10.1039/c2jm13633c.

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20

Saito, Yuta, Tomoya Higashihara, and Mitsuru Ueda. "Direct Photo-patterning of Poly(3-hexylthiophene)." Journal of Photopolymer Science and Technology 24, no. 3 (2011): 273–76. http://dx.doi.org/10.2494/photopolymer.24.273.

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21

Healy, Andrew T., Bryan W. Boudouris, C. Daniel Frisbie, Marc A. Hillmyer, and David A. Blank. "Intramolecular Exciton Diffusion in Poly(3-hexylthiophene)." Journal of Physical Chemistry Letters 4, no. 20 (September 30, 2013): 3445–49. http://dx.doi.org/10.1021/jz401694j.

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22

Dierckx, Wouter, Wibren D. Oosterbaan, Jean-Christophe Bolsée, Ilaria Cardinaletti, Wouter Maes, Hans-Gerd Boyen, Jan D’Haen, Milos Nesladek, and Jean Manca. "Organic phototransistors using poly(3-hexylthiophene) nanofibres." Nanotechnology 26, no. 6 (January 19, 2015): 065201. http://dx.doi.org/10.1088/0957-4484/26/6/065201.

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23

Ahn, H., D. W. Oblas, and J. E. Whitten. "Electron Irradiation of Poly(3-hexylthiophene) Films." Macromolecules 37, no. 9 (May 2004): 3381–87. http://dx.doi.org/10.1021/ma030589x.

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24

Ivanov, Momchil, Jonathan Gross, and Wolfhard Janke. "Single-chain behavior of poly(3-hexylthiophene)." European Physical Journal Special Topics 226, no. 4 (April 2017): 667–81. http://dx.doi.org/10.1140/epjst/e2016-60348-7.

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25

Han, Yuanyuan, Yan Guo, Yingfei Chang, Yanhou Geng, and Zhaohui Su. "Chain Folding in Poly(3-hexylthiophene) Crystals." Macromolecules 47, no. 11 (May 22, 2014): 3708–12. http://dx.doi.org/10.1021/ma5006149.

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26

Kim, Yuna, Yoonjung Kim, Sehwan Kim, and Eunkyoung Kim. "Electrochromic Diffraction from Nanopatterned Poly(3-hexylthiophene)." ACS Nano 4, no. 9 (August 23, 2010): 5277–84. http://dx.doi.org/10.1021/nn1016378.

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27

Källman, K. M., R. Österbacka, H. Stubb, G. Juška, and K. Arlauskas. "Origin of Photocurrent in Poly(3-hexylthiophene)." Synthetic Metals 101, no. 1-3 (May 1999): 581–82. http://dx.doi.org/10.1016/s0379-6779(98)01119-9.

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28

Westerling, M., C. Vijila, R. Österbacka, and H. Stubb. "Bimolecular recombination in regiorandom poly(3-hexylthiophene)." Chemical Physics 286, no. 2-3 (January 2003): 315–20. http://dx.doi.org/10.1016/s0301-0104(02)00930-8.

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29

Trznadel, M., O. Chauvet, M. Lapkowski, and A. Pron. "EPR study of regioregular poly(3-hexylthiophene)." Synthetic Metals 101, no. 1-3 (May 1999): 358. http://dx.doi.org/10.1016/s0379-6779(98)01311-3.

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30

Li, Jianquan, and Koichi Aoki. "Electrochemical gelation of poly(3-hexylthiophene) film." Journal of Electroanalytical Chemistry 453, no. 1-2 (August 1998): 107–12. http://dx.doi.org/10.1016/s0022-0728(98)00238-1.

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31

Chen, Show-An, and Chien-Shiun Liao. "Charge transport in neutral poly(3-hexylthiophene)." Synthetic Metals 60, no. 1 (September 1993): 51–55. http://dx.doi.org/10.1016/0379-6779(93)91183-3.

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32

Linton, J. R., C. W. Frank, and S. D. D. V. Rughooputh. "Fluorescence studies of poly(3-hexylthiophene) solutions." Synthetic Metals 28, no. 1-2 (January 1989): 393–98. http://dx.doi.org/10.1016/0379-6779(89)90551-1.

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33

Holdcroft, Steven. "A photochemical study of poly(3-hexylthiophene)." Macromolecules 24, no. 17 (August 1991): 4834–38. http://dx.doi.org/10.1021/ma00017a017.

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34

Westerling, M., C. Vijila, R. Österbacka, and H. Stubb. "Recombination dynamics in regiorandom poly(3-hexylthiophene)." Synthetic Metals 135-136 (April 2003): 321–22. http://dx.doi.org/10.1016/s0379-6779(02)00612-4.

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35

Shiga, T., A. Okada, and T. Kurauchi. "Electroviscoelastic effect of doped poly(3-hexylthiophene)." Journal of Materials Science Letters 14, no. 7 (1995): 514–15. http://dx.doi.org/10.1007/bf00665919.

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36

Barford, William, David G. Lidzey, Dmitry V. Makhov, and Anthony J. H. Meijer. "Exciton localization in disordered poly(3-hexylthiophene)." Journal of Chemical Physics 133, no. 4 (July 28, 2010): 044504. http://dx.doi.org/10.1063/1.3459099.

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37

Assadi, A., C. Svensson, M. Willander, and O. Inganäs. "Field‐effect mobility of poly(3‐hexylthiophene)." Applied Physics Letters 53, no. 3 (July 18, 1988): 195–97. http://dx.doi.org/10.1063/1.100171.

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38

Yu, G., S. D. Phillips, H. Tomozawa, and A. J. Heeger. "Subnanosecond transient photoconductivity in poly(3-hexylthiophene)." Physical Review B 42, no. 5 (August 15, 1990): 3004–10. http://dx.doi.org/10.1103/physrevb.42.3004.

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39

Fanous, Jean, Michael Schweizer, Dirk Schawaller, and Michael R. Buchmeiser. "Crystalline and Conductive Poly(3-hexylthiophene) Fibers." Macromolecular Materials and Engineering 297, no. 2 (July 26, 2011): 123–27. http://dx.doi.org/10.1002/mame.201100092.

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40

Shaw, Paul E., Arvydas Ruseckas, and Ifor D. W. Samuel. "Exciton Diffusion Measurements in Poly(3-hexylthiophene)." Advanced Materials 20, no. 18 (July 14, 2008): 3516–20. http://dx.doi.org/10.1002/adma.200800982.

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41

Shiga, Tohru, and Akane Okada. "Electroplastic behavior of doped poly(3-hexylthiophene)." Journal of Applied Polymer Science 62, no. 6 (November 7, 1996): 903–10. http://dx.doi.org/10.1002/(sici)1097-4628(19961107)62:6<903::aid-app6>3.0.co;2-t.

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42

Berson, S., R. De Bettignies, S. Bailly, and S. Guillerez. "Poly(3-hexylthiophene) Fibers for Photovoltaic Applications." Advanced Functional Materials 17, no. 8 (April 18, 2007): 1377–84. http://dx.doi.org/10.1002/adfm.200600922.

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43

Wang, H. L., M. Grigorova, E. S. Maniloff, D. W. McBranch, and B. R. Mattes. "Variations in the optical properties of poly-3-hexylthiophene/C60 blends and poly-3-hexylthiophene/sol-gel composites." Synthetic Metals 84, no. 1-3 (January 1997): 253–54. http://dx.doi.org/10.1016/s0379-6779(97)80738-2.

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44

Kim, Seung-Hoi. "Utilization of Zinc Dust for a Core Monomer 2-Bromo-3-hexylthien-5-ylzinc Bromide: Its Synthesis and Application for the Preparation of Regioregular Poly(3-hexylthiophene)." International Journal of Polymer Science 2014 (2014): 1–5. http://dx.doi.org/10.1155/2014/847309.

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The oxidative insertion of readily available zinc dust into the carbon-bromine bond of 2,5-dibromo-3-hexylthiophene was efficiently achieved to provide 2-bromo-3-hexylthien-5-ylzinc bromide (I), which was utilized for the preparation of highly regioregular poly(3-hexylthiophene) (P3HT) in the presence of catalytic amounts of Ni-catalyst.

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45

Jiang, Long, Jianling Zhang, Weiwei Wang, Haigang Yang, Frederic Reisdorffer, Thien-Phap Nguyen, and Yi Dan. "Optical properties of poly(3-hexylthiophene) and interfacial charge transfer between poly(3-hexylthiophene) and titanium dioxide in composites." Journal of Luminescence 159 (March 2015): 88–92. http://dx.doi.org/10.1016/j.jlumin.2014.11.002.

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46

Casalegno, Mosè, Tommaso Nicolini, Antonino Famulari, Guido Raos, Riccardo Po, and Stefano V. Meille. "Atomistic modelling of entropy driven phase transitions between different crystal modifications in polymers: the case of poly(3-alkylthiophenes)." Physical Chemistry Chemical Physics 20, no. 46 (2018): 28984–89. http://dx.doi.org/10.1039/c8cp05820b.

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Atomistic MD simulation allows following continuously the experimentally observed transition between form I and form II poly(3-hexylthiophene) and poly(3-butylthiophene), evidencing unexpected reorganization.

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47

Mohamed, Mohamed Gamal, Chih-Chia Cheng, Yung-Chih Lin, Cheng-Wei Huang, Fang-Hsien Lu, Feng-Chih Chang, and Shiao-Wei Kuo. "Synthesis and self-assembly of water-soluble polythiophene-graft-poly(ethylene oxide) copolymers." RSC Adv. 4, no. 42 (2014): 21830–39. http://dx.doi.org/10.1039/c4ra02433h.

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48

Su, Ming, Sheng-Yu Shi, Qian Wang, Na Liu, Jun Yin, Chunhua Liu, Yunsheng Ding, and Zong-Quan Wu. "Multi-responsive behavior of highly water-soluble poly(3-hexylthiophene)-block-poly(phenyl isocyanide) block copolymers." Polymer Chemistry 6, no. 36 (2015): 6519–28. http://dx.doi.org/10.1039/c5py00988j.

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Highly water-soluble block copolymers containing conjugated poly(3-hexylthiophene) and hydrophilic poly(phenyl isocyanide) segments were found to be responsive to multiple stimuli, such as temperature, pH and solvents.

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49

Nawaz, Ali, Isidro Cruz-Cruz, Rafael Rodrigues, and Ivo A. Hümmelgen. "Performance enhancement of poly(3-hexylthiophene-2,5-diyl) based field effect transistors through surfactant treatment of the poly(vinyl alcohol) gate insulator surface." Physical Chemistry Chemical Physics 17, no. 40 (2015): 26530–34. http://dx.doi.org/10.1039/c4cp02245a.

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50

Deckers, S., S. Vandendriessche, D. Cornelis, F. Monnaie, G. Koeckelberghs, I. Asselberghs, T. Verbiest, and M. A. van der Veen. "Poly(3-alkylthiophene)s show unexpected second-order nonlinear optical response." Chem. Commun. 50, no. 21 (2014): 2741–43. http://dx.doi.org/10.1039/c3cc48099b.

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