钝化
钙钛矿(结构)
材料科学
制作
光伏
图层(电子)
能量转换效率
化学工程
光电子学
纳米技术
载流子寿命
离子
离子键合
无机化学
萃取(化学)
堆栈(抽象数据类型)
锂(药物)
化学物理
作者
C ZHANG,Julian A. Steele,Saivineeth Penukula,Miaoqiang Lyu,Dongxu He,Shanshan Ding,Jin Ye,Sabah Gaznaghi,Huiyuan Cheng,Zi Wang,Hongzhe Xu,Nicholas Rolston,Qunliang Song,Lianzhou Wang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-06-02
标识
DOI:10.1021/acs.nanolett.6c00804
摘要
Molecular passivation of interfacial defects represents a key pathway toward high-performance perovskite solar cells (PSCs), yet its success hinges on the formation of robust and functional bonds with the perovskite lattice. Weak or limited interactions at the perovskite/hole transport layer (HTL) interface often led to insufficient passivation, accelerated ion migration, and compromised morphological stability, ultimately resulting in a rapid performance degradation. Here, we prepare 2-aminothiazoline hydrochloride (ATZCl) as a multifunctional passivator that forms multidentate binding and reconstructs the perovskite surface through the subsequent spontaneous growth of an RP-like surface phase. This synergistic interaction effectively suppresses defect states, minimizes nonradiative recombination, and enhances charge extraction at the critical perovskite/HTL interface. Time-of-flight secondary-ion mass spectrometry analysis corroborates that the ATZCl interlayer significantly suppresses iodine ion migration across the perovskite/HTL stack. Consequently, our strategy enables the all-air fabrication of high-performance PSCs, achieving a champion power conversion efficiency of 25.22% alongside markedly improved operational stability.
科研通智能强力驱动
Strongly Powered by AbleSci AI