Log in

Relevant bibliographies by topics / Organic semiconductors - Design and construction / Journal articles

To see the other types of publications on this topic, follow the link: Organic semiconductors - Design and construction.

Journal articles on the topic 'Organic semiconductors - Design and construction'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Organic semiconductors - Design and construction.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Jiang, He, Jibiao Jin, Zijie Wang, Wuji Wang, Runfeng Chen, Ye Tao, Qin Xue, Chao Zheng, Guohua Xie, and Wei Huang. "Constructing Donor-Resonance-Donor Molecules for Acceptor-Free Bipolar Organic Semiconductors." Research 2021 (February 9, 2021): 1–10. http://dx.doi.org/10.34133/2021/9525802.

Full text

Abstract:

Organic semiconductors with bipolar transporting character are highly attractive as they offer the possibility to achieve high optoelectronic performance in simple device structures. However, the continual efforts in preparing bipolar materials are focusing on donor-acceptor (D-A) architectures by introducing both electron-donating and electron-withdrawing units into one molecule in static molecular design principles. Here, we report a dynamic approach to construct bipolar materials using only electron-donating carbazoles connected by N-P=X resonance linkages in a donor-resonance-donor (D-r-D) structure. By facilitating the stimuli-responsive resonance variation, these D-r-D molecules exhibit extraordinary bipolar properties by positively charging one donor of carbazole in enantiotropic N+=P-X- canonical forms for electron transport without the involvement of any acceptors. With thus realized efficient and balanced charge transport, blue and deep-blue phosphorescent organic light emitting diodes hosted by these D-r-D molecules show high external quantum efficiencies up to 16.2% and 18.3% in vacuum-deposited and spin-coated devices, respectively. These results via the D-r-D molecular design strategy represent an important concept advance in constructing bipolar organic optoelectronic semiconductors dynamically for high-performance device applications.

APA, Harvard, Vancouver, ISO, and other styles

2

Marszalek, Tomasz, Maciej Gazicki-Lipman, and Jacek Ulanski. "Parylene C as a versatile dielectric material for organic field-effect transistors." Beilstein Journal of Nanotechnology 8 (July 28, 2017): 1532–45. http://dx.doi.org/10.3762/bjnano.8.155.

Full text

Abstract:

An emerging new technology, organic electronics, is approaching the stage of large-scale industrial application. This is due to a remarkable progress in synthesis of a variety of organic semiconductors, allowing one to design and to fabricate, so far on a laboratory scale, different organic electronic devices of satisfactory performance. However, a complete technology requires upgrading of fabrication procedures of all elements of electronic devices and circuits, which not only comprise active layers, but also electrodes, dielectrics, insulators, substrates and protecting/encapsulating coatings. In this review, poly(chloro-para-xylylene) known as Parylene C, which appears to become a versatile supporting material especially suitable for applications in flexible organic electronics, is presented. A synthesis and basic properties of Parylene C are described, followed by several examples of use of parylenes as substrates, dielectrics, insulators, or protecting materials in the construction of organic field-effect transistors.

APA, Harvard, Vancouver, ISO, and other styles

3

Feng, Cheng, Xihong Mi, Dingwen Zhong, Weiming Zhang, Yongping Liu, Dayong Fan, Ming Li, Jiefeng Hai, and Zhenhuan Lu. "Chemically Bonded N-PDI-P/WO3 Organic-Inorganic Heterojunction with Improved Photoelectrochemical Performance." Catalysts 10, no. 1 (January 15, 2020): 122. http://dx.doi.org/10.3390/catal10010122.

Full text

Abstract:

The chemical bonding of bandgap adjustable organic semiconductors with inorganic semiconducting materials is effective in constructing a high-performance heterogeneous photoanode. In this study, a new asymmetric perylene diimide derivative molecule (N-PDI-P) was synthesized by connecting tert-butoxycarbonyl on an N-site at one end of a PDI molecule through methylene and connecting naphthalene directly onto the other end. This molecule was bonded onto the WO3 film surface, thereby forming the photoanode of organic-inorganic heterojunction. Under light illumination, the photocurrent density of chemically bonded N-PDI-P/WO3 heterojunction was twofold higher than that of physically adhered heterojunction for photoelectrochemical water oxidation at 0.6 V (vs. Ag/AgCl). Energy band structure and charge transfer dynamic analyses revealed that photogenerated electron carriers on the highest occupied molecular orbital (HOMO) of an N-PDI-P molecule can be transferred to the conduction band of WO3. The charge transfer and separation rates were accelerated considerably after the chemical bond formed at the N-PDI-P/WO3 interface. The proposed method provides a new way for the design and construction of organic-inorganic composite heterojunction.

APA, Harvard, Vancouver, ISO, and other styles

4

Wu, Jieyun, Qing Li, Wen Wang, and Kaixin Chen. "Optoelectronic Properties and Structural Modification of Conjugated Polymers Based on Benzodithiophene Groups." Mini-Reviews in Organic Chemistry 16, no. 3 (January 25, 2019): 253–60. http://dx.doi.org/10.2174/1570193x15666180406144851.

Full text

Abstract:

Organic conjugated materials have shown attractive applications due to their good optoelectronic properties, which enable them solution processing techniques in organic optoelectronic devices. Many conjugated materials have been investigated in polymer solar cells and organic field-effect transistors. Among those conjugated materials, Benzo[1,2-b:4,5-b′]dithiophene (BDT) is one of the most employed fused-ring building groups for the synthesis of conjugated materials. The symmetric and planar conjugated structure, tight and regular stacking of BDT can be expected to exhibit the excellent carrier transfer for optoelectronics. In this review, we summarize the recent progress of BDT-based conjugated polymers in optoelectronic devices. BDT-based conjugated materials are classified into onedimensional (1D) and two-dimensional (2D) BDT-based conjugated polymers. Firstly, we introduce the fundamental information of BDT-based conjugated materials and their application in optoelectronic devices. Secondly, the design and synthesis of alkyl, alkoxy and aryl-substituted BDT-based conjugated polymers are discussed, which enables the construction of one-dimensional and two-dimensional BDTbased conjugated system. In the third part, the structure modification, energy level tuning and morphology control and their influences on optoelectronic properties are discussed in detail to reveal the structure- property relationship. Overall, we hope this review can be a good reference for the molecular design of BDT-based semiconductor materials in optoelectronic devices.

APA, Harvard, Vancouver, ISO, and other styles

5

INOKUCHI, Hiroo. "The construction of novel organic semiconductors." Nihon Kessho Gakkaishi 30, no. 1 (1988): 9–17. http://dx.doi.org/10.5940/jcrsj.30.9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Heimel, Georg, Ingo Salzmann, Steffen Duhm, and Norbert Koch. "Design of Organic Semiconductors from Molecular Electrostatics†." Chemistry of Materials 23, no. 3 (February 8, 2011): 359–77. http://dx.doi.org/10.1021/cm1021257.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Baumeier, Björn, Falk May, Christian Lennartz, and Denis Andrienko. "Challenges for in silico design of organic semiconductors." Journal of Materials Chemistry 22, no. 22 (2012): 10971. http://dx.doi.org/10.1039/c2jm30182b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Henson, Zachary B., Klaus Müllen, and Guillermo C. Bazan. "Design strategies for organic semiconductors beyond the molecular formula." Nature Chemistry 4, no. 9 (August 23, 2012): 699–704. http://dx.doi.org/10.1038/nchem.1422.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Nishida, Jun-ichi, and Yoshiro Yamashita. "Molecular Design of Organic Semiconductors for High Performance Organic Field-effect Transistors." Journal of Synthetic Organic Chemistry, Japan 66, no. 5 (2008): 515–24. http://dx.doi.org/10.5059/yukigoseikyokaishi.66.515.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Okamoto, Toshihiro, Shohei Kumagai, Eiji Fukuzaki, Hiroyuki Ishii, Go Watanabe, Naoyuki Niitsu, Tatsuro Annaka, et al. "Robust, high-performance n-type organic semiconductors." Science Advances 6, no. 18 (May 2020): eaaz0632. http://dx.doi.org/10.1126/sciadv.aaz0632.

Full text

Abstract:

Organic semiconductors (OSCs) are important active materials for the fabrication of next-generation organic-based electronics. However, the development of n-type OSCs lags behind that of p-type OSCs in terms of charge-carrier mobility and environmental stability. This is due to the absence of molecular designs that satisfy the requirements. The present study describes the design and synthesis of n-type OSCs based on challenging molecular features involving a π-electron core containing electronegative N atoms and substituents. The unique π-electron system simultaneously reinforces both electronic and structural interactions. The current n-type OSCs exhibit high electron mobilities with high reliability, atmospheric stability, and robustness against environmental and heat stresses and are superior to other existing n-type OSCs. This molecular design represents a rational strategy for the development of high-end organic-based electronics.

APA, Harvard, Vancouver, ISO, and other styles

11

Mei, Jianguo, Ying Diao, Anthony L. Appleton, Lei Fang, and Zhenan Bao. "Integrated Materials Design of Organic Semiconductors for Field-Effect Transistors." Journal of the American Chemical Society 135, no. 18 (April 26, 2013): 6724–46. http://dx.doi.org/10.1021/ja400881n.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Hathwar, Venkatesha, Mads Jørgensen, Mattia Sist, Jacob Overgaard, Bo Iversen, Xiaoping Wang, Christina Hoffmann, and Alejandro Briseno. "Material Design Inputs from Charge Density Analysis in Organic Semiconductors." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1552. http://dx.doi.org/10.1107/s2053273314084472.

Full text

Abstract:

In recent years, semiconducting organic materials have attracted a considerable amount of interest to develop all-organic or hybrid organic-inorganic electronic devices such as organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), or photovoltaic cells. Rubrene (5,6,11,12-tetraphenyltetracene, RUB) is one of the most explored compound in this area as it has nearly 100% fluorescence quantum efficiency in solution. Additionally, the OFET fabricated by vacuum-deposited using orthorhombic rubrene single crystals show p-type characteristics with high mobility up to 20cm2/Vs (Podzorov et al., 2004). The large charge-carrier mobilities measured have been attributed to the packing motif (Fig a) which provides enough spatial overlap of the π-conjugated tetracene backbone. In the same time, RUB undergoes an oxidation in the presence of light to form rubrene endoperoxide (RUB-OX) (Fumagalli et al., 2011). RUB-OX molecules show electronic and structural properties strikingly different from those of RUB, mainly due to the disruption in the conjugate stacking of tetracene moieties. The significant semiconducting property of RUB is not clear yet. In this context, high resolution single crystal X-ray data of RUB (Fig b) and RUB-OX have been collected at 100K. Owing to the presence of weak aromatic stacking and quadrupolar interactions, the neutron single crystal data is also collected at 100K. The C-H bond distances and scaled anisotropic displacement parameters (ADP) of hydrogens from the neutron experiment are used in the multipolar refinements of electron density. The chemical bonding features (Fig c), the topology of electron density and strength of weak interaction are calculated by the Atoms in Molecules (AIM) theory (Bader, 1990). It is further supported by the source function description and mapping of non-covalent interactions based on the electron density. The detailed comparison of two organic semiconductors, RUB and RUB-OX will be discussed.

APA, Harvard, Vancouver, ISO, and other styles

13

Newman, Christopher R., C. Daniel Frisbie, Demetrio A. da Silva Filho, Jean-Luc Brédas, Paul C. Ewbank, and Kent R. Mann. "Introduction to Organic Thin Film Transistors and Design of n-Channel Organic Semiconductors." Chemistry of Materials 16, no. 23 (November 2004): 4436–51. http://dx.doi.org/10.1021/cm049391x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Klimovich, I. V., L. I. Leshanskaya, S. I. Troyanov, D. V. Anokhin, D. V. Novikov, A. A. Piryazev, D. A. Ivanov, N. N. Dremova, and P. A. Troshin. "Design of indigo derivatives as environment-friendly organic semiconductors for sustainable organic electronics." J. Mater. Chem. C 2, no. 36 (2014): 7621–31. http://dx.doi.org/10.1039/c4tc00550c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Zhao, Wenrui, Jiamin Ding, Ye Zou, Chong-an Di, and Daoben Zhu. "Chemical doping of organic semiconductors for thermoelectric applications." Chemical Society Reviews 49, no. 20 (2020): 7210–28. http://dx.doi.org/10.1039/d0cs00204f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Chen, Mengyun, Lijia Yan, Yang Zhao, Imran Murtaza, Hong Meng, and Wei Huang. "Anthracene-based semiconductors for organic field-effect transistors." Journal of Materials Chemistry C 6, no. 28 (2018): 7416–44. http://dx.doi.org/10.1039/c8tc01865k.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Ortiz, Rocío Ponce, Helena Herrera, Carlos Seoane, José L. Segura, Antonio Facchetti, and Tobin J. Marks. "Rational Design of Ambipolar Organic Semiconductors: Is Core Planarity Central to Ambipolarity in Thiophene-Naphthalene Semiconductors?" Chemistry - A European Journal 18, no. 2 (December 12, 2011): 532–43. http://dx.doi.org/10.1002/chem.201101715.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Jung, Byung Jun, Noah J. Tremblay, Ming-Ling Yeh, and Howard E. Katz. "Molecular Design and Synthetic Approaches to Electron-Transporting Organic Transistor Semiconductors†." Chemistry of Materials 23, no. 3 (February 8, 2011): 568–82. http://dx.doi.org/10.1021/cm102296d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Bronstein, Hugo, Christian B. Nielsen, Bob C. Schroeder, and Iain McCulloch. "The role of chemical design in the performance of organic semiconductors." Nature Reviews Chemistry 4, no. 2 (January 3, 2020): 66–77. http://dx.doi.org/10.1038/s41570-019-0152-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Friederich, Pascal, Artem Fediai, Simon Kaiser, Manuel Konrad, Nicole Jung, and Wolfgang Wenzel. "Organic Semiconductors: Toward Design of Novel Materials for Organic Electronics (Adv. Mater. 26/2019)." Advanced Materials 31, no. 26 (June 2019): 1970188. http://dx.doi.org/10.1002/adma.201970188.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Ward, Jeremy W., Ruipeng Li, Abdulmalik Obaid, Marcia M. Payne, Detlef-M. Smilgies, John E. Anthony, Aram Amassian, and Oana D. Jurchescu. "Organic Semiconductors: Rational Design of Organic Semiconductors for Texture Control and Self-Patterning on Halogenated Surfaces (Adv. Funct. Mater. 32/2014)." Advanced Functional Materials 24, no. 32 (August 2014): 5168. http://dx.doi.org/10.1002/adfm.201470216.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Casalini, Stefano, Carlo Augusto Bortolotti, Francesca Leonardi, and Fabio Biscarini. "Self-assembled monolayers in organic electronics." Chemical Society Reviews 46, no. 1 (2017): 40–71. http://dx.doi.org/10.1039/c6cs00509h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Ling-Hai, XIE, CHANG Yong-Zheng, GU Ju-Fen, SUN Rui-Juan, LI Jie-Wei, ZHAO Xiang-Hua, and HUANG Wei. "Design of Organic/Polymeric π-Semiconductors: the Four-Element Principle." Acta Physico-Chimica Sinica 26, no. 07 (2010): 1784–94. http://dx.doi.org/10.3866/pku.whxb20100713.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Takimiya, Kazuo, Masahiro Nakano, Hiroyoshi Sugino, and Itaru Osaka. "Design and elaboration of organic molecules for high field-effect-mobility semiconductors." Synthetic Metals 217 (July 2016): 68–78. http://dx.doi.org/10.1016/j.synthmet.2016.02.018.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Guo, Xiaojie, Qiaogan Liao, Eric F. Manley, Zishan Wu, Yulun Wang, Weida Wang, Tingbin Yang, et al. "Materials Design via Optimized Intramolecular Noncovalent Interactions for High-Performance Organic Semiconductors." Chemistry of Materials 28, no. 7 (March 15, 2016): 2449–60. http://dx.doi.org/10.1021/acs.chemmater.6b00850.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Kanibolotsky, Alexander L., Nicolas Laurand, Martin D. Dawson, Graham A. Turnbull, Ifor D. W. Samuel, and Peter J. Skabara. "Design of Linear and Star-Shaped Macromolecular Organic Semiconductors for Photonic Applications." Accounts of Chemical Research 52, no. 6 (May 22, 2019): 1665–74. http://dx.doi.org/10.1021/acs.accounts.9b00129.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Jin, Ruifa, Fengxin Wang, Ruijie Guan, Xiaomin Zheng, and Tao Zhang. "Design of perylene-diimides-based small-molecules semiconductors for organic solar cells." Molecular Physics 115, no. 14 (March 30, 2017): 1591–97. http://dx.doi.org/10.1080/00268976.2017.1308028.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Xie, Wenjun, Weicong Huang, Lingzhi Tu, Hu Shi, and Hongguang Liu. "Design of one-dimensional organic semiconductors with high intrinsic electron mobilities: lessons from computation." Journal of Materials Chemistry C 9, no. 10 (2021): 3620–25. http://dx.doi.org/10.1039/d0tc05817c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Thorley, Karl J., and Chad Risko. "Mapping the configuration dependence of electronic coupling in organic semiconductors." Journal of Materials Chemistry C 4, no. 17 (2016): 3825–32. http://dx.doi.org/10.1039/c5tc03765d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Dhar, Joydeep, Ulrike Salzner, and Satish Patil. "Trends in molecular design strategies for ambient stable n-channel organic field effect transistors." Journal of Materials Chemistry C 5, no. 30 (2017): 7404–30. http://dx.doi.org/10.1039/c6tc05467f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Zeng, Xingwei, Dongwei Zhang, Yanan Zhu, Mo Chen, Haibiao Chen, Seiya Kasai, Hong Meng, and Osamu Goto. "Insight into in-plane isotropic transport in anthracene-based organic semiconductors." Journal of Materials Chemistry C 7, no. 45 (2019): 14275–83. http://dx.doi.org/10.1039/c9tc03915e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Niazi, Muhammad Rizwan, Ehsan Hamzehpoor, Pegah Ghamari, Igor F. Perepichka, and Dmitrii F. Perepichka. "Nitroaromatics as n-type organic semiconductors for field effect transistors." Chemical Communications 56, no. 47 (2020): 6432–35. http://dx.doi.org/10.1039/d0cc01236j.

Full text

Abstract:

The utility of the NO₂-group in the design of organic semiconductors is demonstrated by fabricating OFETs with 5 nitrofluorenone derivatives and analyzing the effects of molecular and crystal structure on their charge transport characteristics.

APA, Harvard, Vancouver, ISO, and other styles

33

Yahiro, Masayuki, Tomo Sakanoue, Hiroyuki Uchiuzou, Takahito Oyamada, Akio Toshimitsu, and Chihaya Adachi. "Material Design of Organic Semiconductors for Light Emitting Organic Field-effect Transistors and Their Device Characteristics." Journal of Synthetic Organic Chemistry, Japan 66, no. 5 (2008): 493–503. http://dx.doi.org/10.5059/yukigoseikyokaishi.66.493.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Gao, Xike, and Yunbin Hu. "Development of n-type organic semiconductors for thin film transistors: a viewpoint of molecular design." J. Mater. Chem. C 2, no. 17 (2014): 3099–117. http://dx.doi.org/10.1039/c3tc32046d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Kolaczkowski, Matthew A., Andrés Garzón-Ruiz, Akash Patel, Zhiyuan Zhao, Yunlong Guo, Amparo Navarro, and Yi Liu. "Design and Synthesis of Annulated Benzothiadiazoles via Dithiolate Formation for Ambipolar Organic Semiconductors." ACS Applied Materials & Interfaces 12, no. 47 (November 10, 2020): 53328–41. http://dx.doi.org/10.1021/acsami.0c16056.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Liu, Chang, Ming-Hua Zeng, Yuexing Zhang, Paul M. Lahti, and Dimitrios Maroudas. "Theoretical design of new cyclopentadithiophene-based organic semiconductors with tunable nature and performance." Synthetic Metals 258 (December 2019): 116196. http://dx.doi.org/10.1016/j.synthmet.2019.116196.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Shan, Bowen, and Qian Miao. "Molecular design of n-type organic semiconductors for high-performance thin film transistors." Tetrahedron Letters 58, no. 20 (May 2017): 1903–11. http://dx.doi.org/10.1016/j.tetlet.2017.04.023.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Salzmann, Ingo, Georg Heimel, Martin Oehzelt, Stefanie Winkler, and Norbert Koch. "Molecular Electrical Doping of Organic Semiconductors: Fundamental Mechanisms and Emerging Dopant Design Rules." Accounts of Chemical Research 49, no. 3 (February 8, 2016): 370–78. http://dx.doi.org/10.1021/acs.accounts.5b00438.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Shen, Hong-Yi, Lei He, Ping-Ping Shi, and Qiong Ye. "Lead-free organic–inorganic hybrid semiconductors and NLO switches tuned by dimensional design." Journal of Materials Chemistry C 9, no. 12 (2021): 4338–43. http://dx.doi.org/10.1039/d1tc00278c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Zhang, Chuang, Yongli Yan, Yong Sheng Zhao, and Jiannian Yao. "From Molecular Design and Materials Construction to Organic Nanophotonic Devices." Accounts of Chemical Research 47, no. 12 (October 24, 2014): 3448–58. http://dx.doi.org/10.1021/ar500192v.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Kumari, Anu, Sandeep Kaushal, and Prit Pal Singh. "Bimetallic metal organic frameworks heterogeneous catalysts: Design, construction, and applications." Materials Today Energy 20 (June 2021): 100667. http://dx.doi.org/10.1016/j.mtener.2021.100667.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Kirsch, Peer, Qiong Tong, and Harald Untenecker. "Crystal design using multipolar electrostatic interactions: A concept study for organic electronics." Beilstein Journal of Organic Chemistry 9 (November 5, 2013): 2367–73. http://dx.doi.org/10.3762/bjoc.9.272.

Full text

Abstract:

Using a simple synthetic protocol, heterohexacene analogues with a quadrupolar distribution of partial charges are readily available. In contrast to most other acenes, these compounds crystallize with a slipped-stack, brickwork-like packing which is mainly controlled by electrostatic interactions. This type of packing offers an advantage for organic semiconductors, because it allows more isotropic charge transport compared to the “herring bone” stacking observed for other acenes.

APA, Harvard, Vancouver, ISO, and other styles

43

Mike, Jared F., Jeremy J. Inteman, Arkady Ellern, and Malika Jeffries-EL. "Facile Synthesis of 2,6-Disubstituted Benzobisthiazoles: Functional Monomers for the Design of Organic Semiconductors." Journal of Organic Chemistry 75, no. 2 (January 15, 2010): 495–97. http://dx.doi.org/10.1021/jo9023864.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Pathan, Abrarkhan M., Dhawal H. Agrawal, Pina M. Bhatt, Hitarthi H. Patel, and U. S. Joshi. "Design and Construction of Low Temperature Attachment for Commercial AFM." Solid State Phenomena 209 (November 2013): 137–42. http://dx.doi.org/10.4028/www.scientific.net/ssp.209.137.

Full text

Abstract:

With the rapid advancements in the field of nanoscience and nanotechnology, scanning probe microscopy has become an integral part of a typical R&D lab. Atomic force microscope (AFM) has become a familiar name in this category. The AFM measures the forces acting between a fine tip and a sample. The tip is attached to the free end of a cantilever and is brought very close to a surface. Attractive or repulsive forces resulting from interactions between the tip and the surface will cause a positive or negative bending of the cantilever. The bending is detected by means of a laser beam, which is reflected from the backside of the cantilever. Atomic force microscopy is currently applied to various environments (air, liquid, vacuum) and types of materials such as metal semiconductors, soft biological samples, conductive and non-conductive materials. With this technique size measurements or even manipulations of nano-objects may be performed. An experimental setup has been designed and built such that a commercially available Atomic Force Microscope (AFM) (Nanosurf AG, Easyscan 2) can be operated at cryogenic temperature under vacuum and in a vibration-free environment. The design also takes care of portability and flexibility of AFM i.e. it is very small, light weight and AFM can be used in both ambient and cryogenic conditions. The whole set up was assembled in-house at a fairly low cost. It is used to study the surface structure of nanomaterials. Important perovskite manganite Pr0.7Ca0.3MnO3thin films were studied and results such as morphology, RMS area and line roughness as well as the particle size have been estimated at cryogenic temperature.

APA, Harvard, Vancouver, ISO, and other styles

45

LI, YUNING, and BENG S. ONG. "HIGH MOBILITY CONJUGATED POLYMER SEMICONDUCTORS FOR ORGANIC THIN FILM TRANSISTORS." COSMOS 05, no. 01 (May 2009): 59–77. http://dx.doi.org/10.1142/s0219607709000427.

Full text

Abstract:

Organic thin film transistors (OTFTs) are promising candidates as alternatives to silicon TFTs for applications where light weight, large area and flexibility are required. OTFTs have shown potential for cost effective fabrication using solution deposition techniques under mild conditions. However, two major issues must be addressed prior to the commercialization of OTFT-based electronics: (i) low charge mobilities and (ii) insufficient air stability. This article reviews recent progress in the design and development of thiophene-based polymer semiconductors as channel materials for OTFTs. To date, both high performance p-type and n-type thiophene-based polymers with benchmark charge carrier mobility of > 0.5 cm2 V-1 s-1 have been archived, which bring printed OTFTs one step closer to commercialization.

APA, Harvard, Vancouver, ISO, and other styles

46

Garnier, Francis, Abderrahim Yassar, Ryad Hajlaoui, Gilles Horowitz, Francoise Deloffre, Bernard Servet, Simone Ries, and Patrick Alnot. "Molecular engineering of organic semiconductors: design of self-assembly properties in conjugated thiophene oligomers." Journal of the American Chemical Society 115, no. 19 (September 1993): 8716–21. http://dx.doi.org/10.1021/ja00072a026.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Takimiya, Kazuo, Tatsuya Yamamoto, Hideaki Ebata, and Takafumi Izawa. "Design strategy for air-stable organic semiconductors applicable to high-performance field-effect transistors." Science and Technology of Advanced Materials 8, no. 4 (January 2007): 273–76. http://dx.doi.org/10.1016/j.stam.2007.02.010.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Nakano, Masahiro, Itaru Osaka, Daisuke Hashizume, and Kazuo Takimiya. "α-Modified Naphthodithiophene Diimides—Molecular Design Strategy for Air-Stable n-Channel Organic Semiconductors." Chemistry of Materials 27, no. 18 (September 4, 2015): 6418–25. http://dx.doi.org/10.1021/acs.chemmater.5b02601.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Li, Yuheng, and Kesong Yang. "High-throughput computational design of organic–inorganic hybrid halide semiconductors beyond perovskites for optoelectronics." Energy & Environmental Science 12, no. 7 (2019): 2233–43. http://dx.doi.org/10.1039/c9ee01371g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Zhang, Weifeng, and Gui Yu. "Rational design of diarylethylene-based polymeric semiconductors for high-performance organic field-effect transistors." Journal of Polymer Science Part A: Polymer Chemistry 55, no. 4 (October 21, 2016): 585–603. http://dx.doi.org/10.1002/pola.28391.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!