噻吩
富勒烯
开路电压
聚合物
材料科学
电压
光化学
化学
化学工程
光电子学
纳米技术
有机化学
物理
量子力学
工程类
作者
Huan Wang,Pengjie Chao,Hui Chen,Zhao Mu,Wei Chen,Feng He
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2017-08-01
卷期号:2 (9): 1971-1977
被引量:54
标识
DOI:10.1021/acsenergylett.7b00551
摘要
Here, the chlorinated polymer, PBTCl, have been found to be an efficient donor in non-fullerene PSCs, which showed a blue-shifted absorbance compared to that of its fluorine analog (PTB7-th), and resulted in a more complementary light absorption with non-fullerene acceptor, such as ITIC. Meanwhile, chlorine substitution lowered the HOMO level of PBTCl, which increased the open-circuit voltage of the corresponding polymer-based devices. The 2D GIWAXS analysis illustrated that the PBTCl/ITIC blend film exhibited a “face-on” orientation and scattering features of both PBTCl and ITIC, suggesting that the blend of PBTCl and ITIC was phase separated and formed individual crystalline domains of the donor and acceptor, which promoted charge transfer in the bi-continuous film and eventually elevated the solar energy conversion efficiency. The PBTCl-based non-fullerene PSC exhibited a maximum PCE of 7.57% with a Voc of 0.91 V, which was an approximately 13% increasing in the PCE compared to the fluorine-analog-based device.
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