材料科学
钙钛矿(结构)
纳米技术
单层
基质(水族馆)
光电子学
化学工程
海洋学
地质学
工程类
作者
Bing’e Li,Jun‐Jie Xing,Vlad Budnik,Chuangping Liu,Qinghua Cao,Fengxian Xie,Xiaoli Zhang,Hui Liu,A. Stsiapanau,Xiao Wei Sun
标识
DOI:10.1021/acsami.4c22563
摘要
Inverted perovskite solar cells (PSCs) have achieved great development, contributed by the advance of self-assembled monolayer (SAM) hole-transporting layers (HTLs) due to their distinctive molecular designability. However, SAM HTLs still present challenges of achieving a compact and ordered surface, resulting in vacancies and defects at the interface as well as adversely affecting the growth of perovskites. In this work, we propose a micromolecule postdeposition process to design the SAM HTL interface and form high-quality perovskites to achieve highly efficient inverted PSCs. We introduce etidronic acid (EA) as a postdeposition micromolecule to fill and reduce vacancies at the SAM interface and to improve growing high-quality perovskites. The postdeposition EA can anchor to the substrate through P-OH anchors, occupying vacancies left by MeO-4PACz, and simultaneously create interaction with perovskites by P═O and C-OH functional groups. The micromolecule postdeposition process effectively fills and reduces vacancies at the SAM interface, passivates defects of perovskites, and facilitates carrier transport. Consequently, a champion PCE of 24.42% is achieved for the target PSCs, which is much higher than the efficiency (20.08%) of the control. This research provides a guided and widely applicable strategy for the development of the SAM interface and further advances the performance of PSCs.
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