串联
钙钛矿(结构)
材料科学
钝化
能量转换效率
结晶
理想(伦理)
光电子学
纳米技术
分子
晶界
纳米晶
动力学
接口(物质)
小分子
理论(学习稳定性)
光伏系统
量子效率
降级(电信)
作者
Shuo Wang,Ming‐Xin Li,Ming‐Xin Li,X Z Gong,Zongbao Li,Xinbo Ma,Jiaju Fu,Zhe Jiang,Qingxiang Liu,Yuxin Liu,Fuyi Wang,Ding-Jiang Xue,Li M,Li M,Jin‐Song Hu
标识
DOI:10.1021/acsenergylett.6c00820
摘要
Inverted inorganic CsPbI3 perovskite solar cells (PSCs) hold great promise for stable and efficient tandem photovoltaics, yet their performance lags behind normal (n-i-p) counterparts due to limited film quality, inefficient carrier extraction, and severe defect-mediated recombination. Here, we demonstrate a triple-functional self-assembled molecule (SAM) engineering strategy to tackle these issues simultaneously. By directly incorporating the SAM into the CsPbI3 precursor solution, the SAM spontaneously enriches at the buried interface to form an efficient hole-selective contact. Meanwhile, its strong interaction with perovskite accelerates crystallization kinetics and enables comprehensive passivation of defects at both grain boundaries and interfaces. As a result, inverted CsPbI3 PSCs achieve an efficiency of 21.10% (certified 20.62%). By leveraging the “three-in-one” functionality of the SAM, this strategy endows PSCs with ideal operational stability (retaining 90% of initial efficiency after 680 h of continuous operating at ∼50 °C) and enables 1 cm2 devices to deliver a record-high efficiency of 19.69%.
科研通智能强力驱动
Strongly Powered by AbleSci AI