Targeting ideal acceptor-donor materials based on hexabenzocoronene

被引:5
|
作者
Silva, H. Santos [1 ]
Metz, Sebastian [2 ]
Hiorns, Roger C. [1 ]
Begue, D. [1 ]
机构
[1] Univ Pau & Pays Adour, CNRS, Inst Sci Analyt & Physicochim Environm & Mat, UMR 5254, F-64000 Pau, France
[2] STFC Daresbury Lab, Sci Comp Dept, Warrington WA4 6DF, Cheshire, England
关键词
Hexabenzocoronene; Discotic liquid crystals; Charge dissociation; Organic photovoltaics; MOLECULAR-ORBITAL METHODS; GAUSSIAN-BASIS SETS; HARTREE-FOCK; THERMAL STABILIZATION; PHOTOVOLTAIC CELLS; CORRELATION-ENERGY; POLYMER; EFFICIENCY; APPROXIMATION; ABSORPTION;
D O I
10.1016/j.molstruc.2018.02.067
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of new hybrid donor-acceptor materials based on hexabenzocoronenes (HBC) functionalized with electron donors is investigated by combining a variety of quantum mechanical and molecular dynamic methodologies for use in organic photovoltaic (OPV) devices. Segments of a low band gap alternating copolymer constructed of benzo[1,2-b;3,4-b]dithiophene and thieno[3,4-c]pyrrole-4,6-dione were attached to the conjugated HBC core. The copolymer was chosen for its known high performance in OPVs, and both moieties were singled out due to their exceptional resistance to photo-oxidation, an important requirement for such applications. The macromolecular topology of these systems are expected to induce supra-molecular columns, such as those common to discotic liquid crystals, conducive to the effective percolation of electrons in OPV devices. A challenge with these systems, that of the mixing of the electronic structures of the donor and acceptor moieties that result in excitonic losses and charge recombination, was diminished by trialling a range of linking units. It was found possible to propose ideal donor-acceptor structures with enhanced charge dissociations and transfers in the p-stacking direction for use in OPV and other organic electronic devices. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:442 / 452
页数:11
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