| Literature DB >> 31532877 |
Yongchun Li1,2, Huifeng Meng1,2, Tao Liu3, Yiqun Xiao4, Zhonghai Tang5, Bo Pang1, Yuqing Li1,2, Ying Xiang1, Guangye Zhang6, Xinhui Lu4, Gui Yu5, He Yan3, Chuanlang Zhan2, Jianhua Huang1, Jiannian Yao2.
Abstract
In the field of all-polymer solar cells (all-PSCs), all efficient polymer acceptors that exhibit efficiencies beyond 8% are based on either imide or dicyanoethylene. To boost the development of this promising solar cell type, creating novel electron-deficient units to build high-performance polymer acceptors is critical. A novel electron-deficient unit containing B←N bonds, namely, BNIDT, is synthesized. Systematic investigation of BNIDT reveals desirable properties including good coplanarity, favorable single-crystal structure, narrowed bandgap and downshifted energy levels, and extended absorption profiles. By copolymerizing BNIDT with thiophene and 3,4-difluorothiophene, two novel conjugated polymers named BN-T and BN-2fT are developed, respectively. It is shown that these polymers possess wide absorption spectra covering 350-800 nm, low-lying energy levels, and ambipolar film-transistor characteristics. Using PBDB-T as the donor and BN-2fT as the acceptor, all-PSCs afford an encouraging efficiency of 8.78%, which is the highest for all-PSCs excluding the devices based on imide and dicyanoethylene-type acceptors. Considering that the structure of BNIDT is totally different from these classical units, this work opens up a new class of electron-deficient unit for constructing efficient polymer acceptors that can realize efficiencies beyond 8% for the first time.Entities:
Keywords: B←N bond; all-polymer solar cell; device performance; electron-deficient unit; polymer acceptor
Year: 2019 PMID: 31532877 DOI: 10.1002/adma.201904585
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849