材料科学
钝化
钙钛矿(结构)
单层
磁滞
富勒烯
能量转换效率
溴化物
控制重构
自组装单层膜
光电子学
纳米技术
化学工程
图层(电子)
有机化学
计算机科学
嵌入式系统
工程类
物理
量子力学
化学
作者
Zijing Chen,Yiming Li,Zhenghao Liu,Jiangjian Shi,Bingcheng Yu,Shan Tan,Yuqi Cui,Chengyu Tan,Fubo Tian,Huijue Wu,Yanhong Luo,Dongmei Li,Qingbo Meng
标识
DOI:10.1002/aenm.202202799
摘要
Abstract Self‐assembled monolayers (SAMs) with unique ordered structures and varied anchoring groups have emerged as an excellent interfacial strategy for perovskite solar cells (PSCs). Herein, 3‐carboxypropyl‐triphenyl phosphonium bromide with the participation of the fullerene derivative [6,6]‐phenyl‐C 61 ‐butyric acid (PCBA) as functionalized C‐PCBA SAM, is introduced to stably modify the TiO 2 /perovskite interface. In the meantime, with strong fullerene cage–iodide interaction, ordered C‐PCBA SAM can passivate interfacial defects and improve the electron transportation. A high efficiency of 24.8% and stabilized power output of 23.9%, are achieved with negligible hysteresis, which is among the best performances for TiO 2 planar PSCs. This modified cell also exhibits significantly improved stabilities under different testing conditions; non‐encapsulated devices can maintain 95% of initial efficiency after 1000 h thermal stability testing at 85 °C and 85% after 700 h continuous illumination (≈100 mW cm −2 ) and maximum‐power‐point tracking. This work provides valuable inspiration for developing highly efficient and stable PSCs by using a convenient SAM reconfiguration strategy.
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