材料科学
双功能
退火(玻璃)
带隙
能量转换效率
光伏系统
方解石
钙钛矿(结构)
化学工程
光电子学
冶金
有机化学
化学
工程类
生物
催化作用
生态学
沸石
作者
Chenghao Duan,Feilin Zou,Qiaoyun Wen,Minchao Qin,Jiong Li,Chang Chen,Xinhui Lu,Liming Ding,Keyou Yan
标识
DOI:10.1002/adma.202300503
摘要
Inorganic CsSnI3 with low toxicity and a narrow bandgap is a promising photovoltaic material. However, the performance of CsSnI3 perovskite solar cells (PSCs) is much lower than that of Pb-based and hybrid Sn-based (e.g., CsPbX3 and CH(NH2 )2 SnX3 ) PSCs, which may be attributed to its poor film-forming property and the deep traps induced by Sn4+ . Here, a bifunctional additive carbazide (CBZ) is adapted to deposit a pinhole-free film and remove the deep traps via two-step annealing. The lone electrons of the NH2 and CO units in CBZ can coordinate with Sn2+ to form a dense film with large grains during the phase transition at 80 °C. The decomposition of CBZ can reduce Sn4+ to Sn2+ during annealing at 150 °C to remove the deep traps. Compared with the control device (4.12%), the maximum efficiency of the CsSnI3 :CBZ PSC reaches 11.21%, which is the highest efficiency of CsSnI3 PSC reported to date. A certified efficiency of 10.90% is obtained by an independent photovoltaic testing laboratory. In addition, the unsealed CsSnI3 :CBZ devices maintain initial efficiencies of ≈100%, 90%, and 80% under an inert atmosphere (60 days), standard maximum power point tracking (650 h at 65 °C), and ambient air (100 h), respectively.
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