钙钛矿(结构)
材料科学
串联
光电子学
带隙
钝化
离子
稳健性(进化)
纳米技术
电压
能量转换效率
图层(电子)
光伏
宽禁带半导体
发光二极管
卤化物
作者
Seongju Park,Kim Sh,Yeongyu Kim,Seungbum Hong,Jinwoo Chu,Hyun Woo Jeong,M. H. Park,Yun Seog Lee,Byungha Shin
出处
期刊:Small
[Wiley]
日期:2026-02-02
卷期号:22 (19): e11627-e11627
标识
DOI:10.1002/smll.202511627
摘要
Sn-Pb perovskite solar cells (PSCs) are considered promising candidates for the bottom subcell in all‑perovskite tandem solar cells, due to their low bandgap and potential to approach the Shockley-Queisser limit. However, their practical application is hindered by the facile oxidation of Sn2+ ions and high trap densities. Here, we introduce FA2SnI6 vacancy‑ordered double perovskite (FADP) with excellent stability under environmental conditions, to fabricate highly efficient and stable FA0.7MA0.3Sn0.5Pb0.5I3 Sn-Pb PSCs. A heterodimensional interface is constructed between the Sn-Pb perovskite and the electron transport layer (ETL) by incorporating FADP, which effectively passivates interfacial defects and suppresses non‑radiative recombination, leading to a remarkable enhancement in open‑circuit voltage (VOC). Furthermore, the n‑type nature of FADP induces favorable band alignment at the Sn-Pb perovskite/ETL interface, and its environmental robustness contributes directly to enhanced device stability. As a result, the champion Sn-Pb PSC achieved a power‑conversion efficiency (PCE) of 22.21% and maintained 91% of its initial PCE after 600 h of storage under nitrogen, highlighting the potential applicability of FADP.
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