Shuai You, Hongwei Zhu, Zhongjin Shen, Xiaoming Wang, Bingyao Shao, Qingxiao Wang, Jianxun Lu, Youyou Yuan, Benjia Dak Dou, Erin M. Sanehira, Todd Russell, Adam Lorenz, Yifan Dong, Lei Chen, Marco Casareto, Nicholas Rolston, Matthew C. Beard, Joseph J. Berry, Marina Freitag, Yanfa Yan, Osman M. Bakr, Kai Zhu
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引用次数: 0
Abstract
Although buckminsterfullerene (C60) is usually the electron transport layer (ETL) in inverted perovskite solar cells (PSCs), its molecular nature leads to weak interfaces that result in nonideal interfacial electronic and mechanical degradation. In this study, we synthesized an ionic salt from C60, 4-(1′,5′-dihydro-1′-methyl-2′H-[5,6] fullereno-C60-Ih-[1,9-c]pyrrol-2′-yl) phenylmethanaminium chloride (CPMAC), and used it as the electron shuttle in inverted PSCs. The CH2-NH3+ head group in the CPMA cation improved the ETL interface, and the ionic nature enhanced the packing, leading to a ~threefold increase in the interfacial toughness compared with that of C60. Using CPMAC, we obtained ~26% power conversion efficiencies (PCEs) with ~2% degradation after 2100 hours of 1-sun operation at 65°C. For minimodules (four subcells, 6 square centimeters), we achieved a PCE of ~23% with <9% degradation after 2200 hours of operation at 55°C.
虽然c60通常是倒置钙钛矿太阳能电池中的电子传递层(ETL),但其分子性质导致弱界面,导致非理想的界面电子和机械退化。本文以c60,4 -(1',5 '-二氢-1'-甲基-2' H -[5,6]富勒烯- c60,4 - I H -[1,9- C]吡咯-2'-基)苯基甲基氯化铵(CPMAC)为原料合成了离子盐,并将其用作反向PSCs的电子穿梭体。CPMA阳离子中的ch2 - nh3 +头基团改善了ETL界面,离子性质增强了填料,使界面韧性比c60提高了约3倍。使用CPMAC,我们在65°C下1太阳运行2,100小时后获得了~26%的功率转换效率(pce)和~2%的退化。对于微型模块(四个亚电池,6厘米平方),在55°C下运行2200小时后,我们实现了~23%的PCE和<;9%的降解。
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