Synergistic Effect of Lewis Base Polymers and Graphene in Enhancing the Efficiency of Perovskite Solar Cells

被引:25
|
作者
Lou, Qiang [1 ]
Lou, Gang [2 ]
Peng, Ruixiang [2 ]
Liu, Zhaoping [2 ]
Wang, Wei [2 ]
Ji, Mingxing [1 ]
Chen, Chong [1 ]
Zhang, Xiaoli [3 ]
Liu, Chang [2 ]
Ge, Ziyi [2 ]
机构
[1] Henan Univ, Henan Key Lab Photovolta Mat, Kaifeng 475004, Peoples R China
[2] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Ningbo 315201, Peoples R China
[3] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Peoples R China
基金
美国国家科学基金会; 国家重点研发计划; 中国国家自然科学基金;
关键词
organic-inorganic hybrid perovskite; Lewis base polymers; graphene; stability and efficiency; p-doping; STABILITY; PERFORMANCE; HYSTERESIS;
D O I
10.1021/acsaem.1c00299
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
Incorporating Lewis base polymers into a perovskite layer has been demonstrated as one of the most effective routes to passivate trap states at the grain boundaries, whereas the inferior electrical conductivity of polymers than that of perovskite would inevitably hinder charge transport across the perovskite grains. Herein, we reported a strategy of utilizing highly conductive graphene/Lewis base polymer (PM6 or PM7) composites as additives in perovskite, which simultaneously passivates the defects and facilitates charge transport in the film. We further revealed in the work that halogen elements (Cl/F) in the polymer (PM6/PM7) can p-dope the graphene and endow it with higher hole-transport selectivity, which is of critical importance as ambipolar charge transport without selectivity would induce significant charge recombination in graphene. By this design, we achieved an outstanding efficiency of 21.21%, which is significantly higher than that of the pristine device without treatment. The device also exhibited impressive stability by retaining 90% of its initial power conversion efficiency after 480 h aging in ambient air with a similar to 35% relative humidity at room temperature.
引用
收藏
页码:3928 / 3936
页数:9
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