Literature DB >> 28608673

Organic Donor-Acceptor Complexes as Novel Organic Semiconductors.

Jing Zhang1, Wei Xu2,3, Peng Sheng4, Guangyao Zhao4, Daoben Zhu2,3.   

Abstract

Organic donor-acceptor (DA) complexes have attracted wide attention in recent decades, resulting in the rapid development of organic binary system electronics. The design and synthesis of organic DA complexes with a variety of component structures have mainly focused on metallicity (or even superconductivity), emission, or ferroelectricity studies. Further efforts have been made in high-performance electronic investigations. The chemical versatility of organic semiconductors provides DA complexes with a great number of possibilities for semiconducting applications. Organic DA complexes extend the semiconductor family and promote charge separation and transport in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). In OFETs, the organic complex serves as an active layer across extraordinary charge pathways, ensuring the efficient transport of induced charges. Although an increasing number of organic semiconductors have been reported to exhibit good p- or n-type properties (mobilities higher than 1 or even 10 cm2 V-1 s-1), critical scientific challenges remain in utilizing the advantages of existing semiconductor materials for more and wider applications while maintaining less complicated synthetic or device fabrication processes. DA complex materials have revealed new insight: their unique molecular packing and structure-property relationships. The combination of donors and acceptors could offer practical advantages compared with their unimolecular materials. First, growing crystals of DA complexes with densely packed structures will reduce impurities and traps from the self-assembly process. Second, complexes based on the original structural components could form superior mixture stacking, which can facilitate charge transport depending on the driving force in the coassembly process. Third, the effective use of organic semiconductors can lead to tunable band structures, allowing the operation mode (p- or n-type) of the transistor to be systematically controlled by changing the components. Finally, theoretical calculations based on cocrystals with unique stacking could widen our understanding of structure-property relationships and in turn help us design high-performance semiconductors based on DA complexes. In this Account, we focus on discussing organic DA complexes as a new class of semiconducting materials, including their design, growth methods, packing modes, charge-transport properties, and structure-property relationships. We have also fabricated and investigated devices based on these binary crystals. This interdisciplinary work combines techniques from the fields of self-assembly, crystallography, condensed-matter physics, and theoretical chemistry. Researchers have designed new complex systems, including donor and acceptor compounds that self-assemble in feasible ways into highly ordered cocrystals. We demonstrate that using this crystallization method can easily realize ambipolar or unipolar transport. To further improve device performance, we propose several design strategies, such as using new kinds of donors and acceptors, modulating the energy alignment of the donor (ionization potential, IP) and acceptor (electron affinity, EA) components, and extending the π-conjugated backbones. In addition, we have found that when we use molecular "doping" (2:1 cocrystallization), the charge-transport nature of organic semiconductors can be switched from hole-transport-dominated to electron-transport-dominated. We expect that the formation of cocrystals through the complexation of organic donor and acceptor species will serve as a new strategy to develop semiconductors for organic electronics with superior performances over their corresponding individual components.

Entities:  

Year:  2017        PMID: 28608673     DOI: 10.1021/acs.accounts.7b00124

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  18 in total

Review 1.  Development of photolabile protecting groups and their application to the optochemical control of cell signaling.

Authors:  Anirban Bardhan; Alexander Deiters
Journal:  Curr Opin Struct Biol       Date:  2019-05-25       Impact factor: 6.809

2.  The sensitivity of donor - acceptor charge transfer to molecular geometry in DAN - NDI based supramolecular flower-like self-assemblies.

Authors:  Mohammad Al Kobaisi; Rajesh S Bhosale; Mohamed E El-Khouly; Duong Duc La; Sachin D Padghan; Sidhanath V Bhosale; Lathe A Jones; Frank Antolasic; Shunichi Fukuzumi; Sheshanath V Bhosale
Journal:  Sci Rep       Date:  2017-11-28       Impact factor: 4.379

3.  Solvation-Enhanced Intermolecular Charge Transfer Interaction in Organic Cocrystals: Enlarged C-C Surface Close Contact in Mixed Packing between PTZ and TCNB.

Authors:  Jing Wang; Aisen Li; Shuping Xu; Chongping Song; Yijia Geng; Ling Ye; Houyu Zhang; Weiqing Xu
Journal:  ACS Omega       Date:  2019-06-17

4.  A Comparative Computational Study of the Adsorption of TCNQ and F4-TCNQ on the Coinage Metal Surfaces.

Authors:  Roberto Otero; Rodolfo Miranda; José M Gallego
Journal:  ACS Omega       Date:  2019-10-04

5.  Aggregation-Induced Fluorescence of Carbazole and o-Carborane Based Organic Fluorophore.

Authors:  Jiemin Jiao; Jia-Xin Kang; Yanna Ma; Qianyi Zhao; Huizhen Li; Jie Zhang; Xuenian Chen
Journal:  Front Chem       Date:  2019-11-15       Impact factor: 5.221

6.  Organic multicomponent microparticle libraries.

Authors:  Dandan Zhang; Jianbo De; Yilong Lei; Hongbing Fu
Journal:  Nat Commun       Date:  2021-03-23       Impact factor: 14.919

7.  Charge-transfer biexciton annihilation in a donor-acceptor co-crystal yields high-energy long-lived charge carriers.

Authors:  Itai Schlesinger; Natalia E Powers-Riggs; Jenna L Logsdon; Yue Qi; Stephen A Miller; Roel Tempelaar; Ryan M Young; Michael R Wasielewski
Journal:  Chem Sci       Date:  2020-08-13       Impact factor: 9.825

8.  Two-photon excited deep-red and near-infrared emissive organic co-crystals.

Authors:  Yu Wang; Huang Wu; Penghao Li; Su Chen; Leighton O Jones; Martín A Mosquera; Long Zhang; Kang Cai; Hongliang Chen; Xiao-Yang Chen; Charlotte L Stern; Michael R Wasielewski; Mark A Ratner; George C Schatz; J Fraser Stoddart
Journal:  Nat Commun       Date:  2020-09-15       Impact factor: 14.919

9.  Band Engineering and Majority Carrier Switching in Isostructural Donor-Acceptor Complexes DPTTA-F X TCNQ Crystals (X = 1, 2, 4).

Authors:  Yingying Liang; Yunke Qin; Jie Chen; Weilong Xing; Ye Zou; Yimeng Sun; Wei Xu; Daoben Zhu
Journal:  Adv Sci (Weinh)       Date:  2019-11-26       Impact factor: 16.806

10.  Pentacene derivative/DTTCNQ cocrystals: alkyl-confined mixed heterojunctions with molecular alignment and transport property tuning.

Authors:  Yudong Ma; Yecheng Zhou; Jianqun Jin; Wei Wang; Xitong Liu; Haixiao Xu; Jing Zhang; Wei Huang
Journal:  Chem Sci       Date:  2019-10-14       Impact factor: 9.825

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