材料科学
串联
钙钛矿(结构)
能量转换效率
带隙
锡
光电子学
纳米技术
化学工程
冶金
复合材料
工程类
作者
Doyun Im,Passarut Boonmongkolras,Yeonghun Yun,Sung Woong Yang,Sunwoo Kim,Jungchul Yun,Rajendra Kumar Gunasekaran,You‐Hyun Seo,Nam Joong Jeon,Gill Sang Han,Sang-Wook Lee
标识
DOI:10.1002/advs.202411403
摘要
Abstract Narrow‐bandgap (NBG) Sn–Pb mixed perovskite solar cells (PSCs) represent a promising solution for surpassing the radiative efficiency of single‐junction solar cells. The unique bandgap tunability of halide perovskites enables optimal tandem configurations of wide‐bandgap (WBG) and NBG subcells. However, these devices are limited by the susceptibility of Sn 2+ in the NBG bottom cell to being oxidized to Sn 4+ , creating detrimental Sn vacancies. Herein, a novel approach that replaces Sn particles with Ni particles is introduced as the reducing agent for Sn–Pb mixed perovskite precursor solutions. The ferromagnetic properties of Ni enable simple magnetic filtration, eliminating the filtration issues associated with Sn particles. Ni particles can be reused up to five times without significantly affecting the PSC's performance. Additionally, Ni effectively mitigates the oxidation of Sn 2+ due to its low reduction potential (−0.23 V), thereby enhancing device performance. Single‐junction Sn–Pb mixed PSCs prepared using Ni achieve a power‐conversion efficiency (PCE) of 22.29%, retaining over 90% of their initial efficiency after 1250 h. Furthermore, Ni‐based all‐perovskite tandem solar cells combining 1.77 eV WBG top cells with 1.25 eV NBG bottom cells achieve a remarkable PCE of 28.13%. Thus, the proposed strategy can facilitate the commercialization of all‐perovskite tandem devices.
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