Stabilizing Lead Halide Perovskites via an Organometallic Chemical Bridge for Efficient and Stable Photovoltaics

被引:4
|
作者
Guo, Junjun [1 ,2 ]
Wang, Bei [1 ,2 ]
Min, Jie [3 ]
Shi, Junwei [1 ,2 ]
Wang, Yao [1 ,2 ]
Ling, Xufeng [1 ,2 ]
Shi, Yafei [1 ,2 ]
Ullah, Ihsan [1 ,2 ]
Chu, Dewei [3 ]
Ma, Wanli [1 ,2 ]
Yuan, Jianyu [1 ,4 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Jiangsu, Peoples R China
[2] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Jiangsu, Peoples R China
[3] Univ New South Wales UNSW, Sch Mat Sci & Engn, Sydney, NSW 2052, Australia
[4] Soochow Univ, Jiangsu Key Lab Adv Negat Carbon Technol, Suzhou 215123, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
organometallic molecule; perovskite solar cells; surface reconstruction; carrier transport; stability; SOLAR-CELLS; PASSIVATION;
D O I
10.1021/acsnano.4c07093
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Defects around the surface and grain boundaries of perovskite films normally cause severe nonradiative recombination and imbalanced charge carrier transport, further limiting both the efficiency and stability of perovskite solar cells (PSCs). To tackle this critical issue, we propose a chemical bridge strategy to reconstruct the interface using organometallic molecules. The commercially available molecule bis(diphenylphosphino)ferrocene (FcP(2)), with a unique bridge molecular structure, anchors and chelates Pb atoms by forming strong Pb-P bonds and further passivates both surfaces and grain boundaries. Detailed characterization revealed that bridge molecule FcP(2) reconstruction can effectively suppress nonradiative recombination, and the electron delocalization properties of the ferrocene core can further achieve more balanced interfacial carrier transport. The resultant N-i-P PSC device outputs close to 25% efficiency together with one of the best reported operational stabilities, maintaining over 95% of the initial efficiency after 1000 h of continuous operation at the maximum power point under 1-sun illumination.
引用
收藏
页码:19865 / 19874
页数:10
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