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Relevant bibliographies by topics / Semiconducting Polymer Molecules

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Journal articles

Academic literature on the topic 'Semiconducting Polymer Molecules'

Author: Grafiati

Published: 7 September 2023

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Journal articles on the topic "Semiconducting Polymer Molecules"

1

Park, Keon Joo, Chae Won Kim, Min Jae Sung, Jiyoul Lee, and Young Tea Chun. "Semiconducting Polymer Nanowires with Highly Aligned Molecules for Polymer Field Effect Transistors." Electronics 11, no. 4 (2022): 648. http://dx.doi.org/10.3390/electronics11040648.

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Conjugated polymers have emerged as promising materials for next-generation electronics. However, in spite of having several advantages, such as a low cost, large area processability and flexibility, polymer-based electronics have their own limitations concerning low electrical performance. To achieve high-performance polymer electronic devices, various strategies have been suggested, including aligning polymer backbones in the desired orientation. In the present paper, we report a simple patterning technique using a polydimethylsiloxane (PDMS) mold that can fabricate highly aligned nanowires

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2

Zhang, Yue, Fangmao Ye, Wei Sun, et al. "Light-induced crosslinkable semiconducting polymer dots." Chemical Science 6, no. 3 (2015): 2102–9. http://dx.doi.org/10.1039/c4sc03959a.

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3

Salaneck, W. R., and M. Fahlman. "Hybrid interfaces of conjugate polymers: Band edge alignment studied by ultraviolet photoelectron spectroscopy." Journal of Materials Research 19, no. 7 (2004): 1917–23. http://dx.doi.org/10.1557/jmr.2004.0262.

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The control of hybrid interfaces in polymer-based electronic devices may be enabling in many applications. The engineering of hybrid interface involves (requires) an understanding of the electronic structure of materials—one organic and one inorganic—that form the two halves of hybrid interfaces, as well as the electronic and chemical consequences of the coupling of the two. Although much literature exists describing the interfaces between vapor-deposited organic molecules and model molecules for polymers on the surfaces of clean metals in ultrahigh vacuum, few studies have been reported on sp

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4

Machatschek, Rainhard, Patrick Ortmann, Renate Reiter, Stefan Mecking, and Günter Reiter. "Assembling semiconducting molecules by covalent attachment to a lamellar crystalline polymer substrate." Beilstein Journal of Nanotechnology 7 (June 2, 2016): 784–98. http://dx.doi.org/10.3762/bjnano.7.70.

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We have investigated the potential of polymers containing precisely spaced side-branches for thin film applications, particularly in the context of organic electronics. Upon crystallization, the side-branches were excluded from the crystalline core of a lamellar crystal. Thus, the surfaces of these crystals were covered by side-branches. By using carboxyl groups as side-branches, which allow for chemical reactions, we could functionalize the crystal with semiconducting molecules. Here, we compare properties of crystals differing in size: small nanocrystals and large single crystals. By assembl

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5

Kweon, O. Young, Moo Yeol Lee, Teahoon Park, et al. "Highly flexible chemical sensors based on polymer nanofiber field-effect transistors." Journal of Materials Chemistry C 7, no. 6 (2019): 1525–31. http://dx.doi.org/10.1039/c8tc06051g.

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6

Garnier, Francis, Fayçal Kouki, Rhiad Hajlaoui, and Gilles Horowitz. "Tunneling at Organic/Metal Interfaces in Oligomer-Based Thin-Film Transistors." MRS Bulletin 22, no. 6 (1997): 52–56. http://dx.doi.org/10.1557/s0883769400033637.

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Organic semiconductors have been studied since the early 1950s, and the large amount of work devoted to them has allowed a better understanding of their charge-transport properties. However owing to their very poor semiconducting characteristics, they were merely considered as exotic materials with little potential interest for applications until the late 1980s, when two significant steps simultaneously appeared in the literature. Richard Friend's group showed that light-emitting diodes could be made from a conjugated semiconducting polymer, and our laboratory showed that efficient field-effec

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7

Kang, Minji, Jun-Seok Yeo, Won-Tae Park, et al. "Favorable Molecular Orientation Enhancement in Semiconducting Polymer Assisted by Conjugated Organic Small Molecules." Advanced Functional Materials 26, no. 46 (2016): 8527–36. http://dx.doi.org/10.1002/adfm.201603617.

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8

Barbosa, Hélder M. C., and Marta M. D. Ramos. "Computer Simulation of Hole Distribution in Polymeric Materials." Materials Science Forum 587-588 (June 2008): 711–15. http://dx.doi.org/10.4028/www.scientific.net/msf.587-588.711.

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Polymers have been known for their flexibility and easy processing into coatings and films, which made them suitable to be applied in a variety of areas and in particular the growing area of organic electronics. The electronic properties of semiconducting polymers made them a serious rival in areas where until now inorganic materials were the most used, such as light emitting diodes or solar cells. Typical polymers can be seen as a network of molecular strands of varied lengths and orientations, with a random distribution of physical and chemical defects which makes them an anisotropic materia

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9

Kietzke, Thomas. "Recent Advances in Organic Solar Cells." Advances in OptoElectronics 2007 (March 23, 2007): 1–15. http://dx.doi.org/10.1155/2007/40285.

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Solar cells based on organic semiconductors have attracted much attention. The thickness of the active layer of organic solar cells is typically only 100 nm thin, which is about 1000 times thinner than for crystalline silicon solar cells and still 10 times thinner than for current inorganic thin film cells. The low material consumption per area and the easy processing of organic semiconductors offer a huge potential for low cost large area solar cells. However, to compete with inorganic solar cells the efficiency of organic solar cells has to be improved by a factor of 2-3. Several organic sem

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10

Lau, W. M., Z. Zheng, Y. H. Wang, et al. "Cross-linking organic semiconducting molecules by preferential C-H cleavage via “chemistry with a tiny hammer”." Canadian Journal of Chemistry 85, no. 10 (2007): 859–65. http://dx.doi.org/10.1139/v07-101.

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In the context of collision-induced dissociation in chemistry and kinematics in physics, we have determined that a beam of hyperthermal protons can be used as tiny hammers to preferentially break the C-H bonds of hydrocarbon precursor molecules adsorbed on a conductive substrate with little damage to other chemical bonds. The activated molecules are thereby converted to a cross-linked molecular network, with its chemical properties tailored by the preservation of the chemical functional groups of the precursors and with its physical properties tuned by the degree of cross-linking. This chemis

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