材料科学
酰亚胺
碱土金属
钙钛矿(结构)
锂(药物)
化学工程
能量转换效率
无机化学
冶金
高分子化学
光电子学
金属
医学
工程类
内分泌学
化学
作者
Ngoc Duy Pham,Jing Shang,Yang Yang,Minh Tam Hoang,Vincent Tiing Tiong,Xiaoxiang Wang,Lijuan Fan,Peng Chen,Liangzhi Kou,Lianzhou Wang,Hongxia Wang
出处
期刊:Nano Energy
[Elsevier BV]
日期:2019-12-20
卷期号:69: 104412-104412
被引量:71
标识
DOI:10.1016/j.nanoen.2019.104412
摘要
Environmental instability of Spiro-OMeTAD-based hole transport layer (HTL) caused due to rapid aggregation and hydration of its additive, Lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI), gives rise to an accelerated degradation of the resulting perovskite solar cells (PSCs). Herein, we show that replacing the Li-TFSI with the more hydrophobic alkaline-earth bis(trifluoromethanesulfonyl)imide additives, namely Mg-TFSI2 and Ca-TFSI2, can effectively stabilize the coordination complexes between the TFSI-salts and 4-tert-Butylpyridine, which in turn results in retarded additive aggregation and hydration, enabling enhanced moisture-resistance of the subsequent HTLs. Moreover, by manipulating this substitution method, we achieved high-quality HTLs with increased hole mobility, better-formed interface with the adjacent perovskite, allowing improved hole extraction process. Incorporating these HTLs into photovoltaic devices, we obtained a substantial performance improvement, with the champion PSC yielded a power conversion efficiency of over 20%. In addition, un-encapsulated devices stabilized by the alkaline-earth bis(trifluoromethanesulfonyl)imide additive maintained 83% its initial efficiency for 193 days after aging in ambient air (RH% = 55–70%).
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