An energy and charge transfer synergetic donor-acceptor heterostructure 2D-COF in photovoltaics

被引:28
|
作者
Yao, Linli [1 ]
Zhang, Yuexing [1 ]
Wang, Hang-Xing [1 ,2 ]
Guo, Yun [1 ]
Zhuang, Zi-Min [1 ]
Wen, Wei [1 ]
Zhang, Xiuhua [1 ]
Wang, Shengfu [1 ]
机构
[1] Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Key Lab Synth & Applicat Organ Funct Mol MOE, Coll Chem & Chem Engn, Wuhan 430062, Peoples R China
[2] Hubei Normal Univ, Hubei Key Lab Pollutant Anal & Reuse Technol, Huangshi 435000, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
COVALENT ORGANIC FRAMEWORK; POLYMER SOLAR-CELLS; VISIBLE-LIGHT; ELECTRON-TRANSFER; CONJUGATED POLYMERS; HETEROJUNCTION; EFFICIENCY; CRYSTALLINE; NITROGEN; DOTS;
D O I
10.1039/d0ta00818d
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
The formation of orderly p-n heterojunctions by the wafer-scale alignment of donor (D) and acceptor (A) molecules, important to achieve high photocurrent generation in the organic semiconductor-based organization, remains a challenging topic. Presented herein is a distinctive D-A heterostructure two-dimensional organic covalent framework (2D-COF) as an efficient organic photovoltaic (OPV) film, supported by the triple roles of the binary building blocks in a wafer-scale film growing at the water/oil interface, molecular level morphology control, and the synergistic Forster resonance energy transfer (FRET) and charge-transfer (CT) functions. The achieved D-A heterostructure 2D-COF has a wafer-scale size, efficient spectral response, and effective separation of photogenerated electron-hole pairs, resulting in an efficient photocurrent generation which is much larger than those of reported OPV COF materials. The achievement herein confirms that the marriage of FRET and a CT synergetic D-A heterostructure and an ultrathin 2D-COF film offer unparalleled advantages in OPV.
引用
收藏
页码:8518 / 8526
页数:9
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