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,Xueyuan Gong,Zongbao Li,Xinbo Ma,Jiaju Fu,Zhe Jiang,Qingxiang Liu,Yuxin Liu,Fuyi Wang,Ding‐Jiang Xue,Ming-Hua Li,Jin‐Song Hu
标识
DOI:10.1021/acsenergylett.6c00820
摘要
Inverted inorganic CsPbI 3 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 CsPbI 3 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 CsPbI 3 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 cm 2 devices to deliver a record-high efficiency of 19.69%.
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