钙钛矿(结构)
螯合作用
齿合度
能量转换效率
材料科学
光伏系统
配体(生物化学)
图层(电子)
化学工程
钙钛矿太阳能电池
纳米技术
金属
化学
无机化学
结晶学
光电子学
冶金
受体
工程类
生物
生物化学
生态学
作者
Jiali Liu,Tengteng Yang,Zhuo Xu,Wangen Zhao,Yan Yang,Yuankun Fang,Lu Zhang,Jingru Zhang,Ningyi Yuan,Jianning Ding,Shengzhong Liu
标识
DOI:10.1002/smtd.202201063
摘要
Solar cell efficiency and stability are two key metrics to determine whether a photovoltaic device is viable for commercial applications. The surface termination of the perovskite layer plays a pivotal role in not only the photoelectric conversion efficiency (PCE) but also the stability of assembled perovskite solar cells (PSCs). Herein, a strong chelate coordination bond is designed to terminate the surface of the perovskite absorber layer. On the one hand, the ligand anions bind with Pb cations via a bidentate chelating bond to restrict the ion migration, and the chelate surface termination changes the surface from hydrophilic to hydrophobic. Both are beneficial to improving the long-term stability. On the other hand, the formation of the chelating bonding effectively eliminates the deep-level defects including PbI and Pb clusters on the Pb-I and FA-I terminations, respectively, as confirmed by theoretical simulation and experimental results. Consequently, the PCE is increased to 24.52%, open circuit voltage to 1.19 V, and fill factor to 81.53%; all three are among the highest for hybrid perovskite cells. The present strategy provides a straightforward means to enhance both the PCE and long-term stability of PSCs.
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