钙钛矿(结构)
正交晶系
单独一对
材料科学
SN2反应
锡
结晶学
化学
立体化学
晶体结构
冶金
有机化学
分子
作者
Tao Ye,Xizu Wang,Kai Wang,Shaoyang Ma,Dong Yang,Yu Hou,Jungjin Yoon,Ke Wang,Shashank Priya
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-03-25
卷期号:: 1480-1489
被引量:218
标识
DOI:10.1021/acsenergylett.1c00342
摘要
Black orthorhombic (B-γ) CsSnI3 with low toxicity and excellent optoelectronic properties is a promising candidate for perovskite solar cell (PSC). However, the performance of the B-γ CsSnI3-based PSCs is much lower than their lead-based or organotin-based counterparts due to the heavy self-doping of Sn2+ to form Sn4+ under ambient-air conditions. Here, this undesirable oxidation in CsSnI3 is restricted by engineering the localized electron density with phthalimide (PTM) additive. The lone electron pairs of NH and two CO units of PTM are designed to form trigeminal coordination bonding with Sn2+, resulting in reduced defect density and relatively grain-ordered perovskite film. The champion efficiencies of 10.1% and 9.6% are obtained for the modified rigid and flexible B-γ CsSnI3-based PSCs, respectively. These encapsulated devices maintain 94.3%, 83.4%, and 81.3% of their initial efficiencies under inert (60 days), ambient (45 days), and 1 Sun continuous illumination at ∼70 °C (2000 min) conditions, respectively.
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