In Situ Buried Interface Engineering towards Printable Pb-Sn Perovskite Solar Cells

被引:4
|
作者
Pious, Johnpaul K. [1 ]
Lai, Huagui [1 ]
Hu, Juntao [2 ]
Luo, Deying [3 ]
Gilshtein, Evgeniia [1 ]
Siegrist, Severin [1 ]
Kothandaraman, Radha K. [1 ]
Lu, Zheng-Hong [2 ,3 ]
Wolff, Christian M. [4 ]
Tiwari, Ayodhya N. [1 ]
Fu, Fan [1 ]
机构
[1] Empa Swiss Fed Labs Mat Sci & Technol, Lab Thin Films & Photovolta, CH-8600 Dubendorf, Switzerland
[2] Yunnan Univ, Ctr Optoelect Engn Res, Dept Phys, Kunming 650091, Yunnan, Peoples R China
[3] Univ Toronto, Dept Mat Sci & Engn, Toronto, ON M5S 3E4, Canada
[4] Ecole Polytech Fed Lausanne EPFL, Inst Elect & Microengn IEM, Photovolta & Thin Film Elect Lab, CH-2002 Neuchatel, Switzerland
关键词
low bandgap Pb-Sn perovskites; buried interface; 2-fluoro benzylammonium iodide additive; perovskitesolar cell upscaling; blade-coating;
D O I
10.1021/acsami.4c07083
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
High-efficiency Pb-Sn narrow-bandgap perovskite solar cells (PSCs) heavily rely on PEDOT:PSS as the hole-transport layer (HTL) owing to its excellent electrical conductivity, dopant-free nature, and facile solution processability. However, the shallow work function (W-F) of PEDOT:PSS consequently results in severe minority carrier recombination at the perovskite/HTL interface. Here, we tackle this issue by an in situ interface engineering strategy using a new molecule called 2-fluoro benzylammonium iodide (FBI) that suppresses nonradiative recombination near the Pb-Sn perovskite (FA(0.6)MA(0.4)Pb(0.4)Sn(0.6)I(3))/HTL bottom interface. The W-F of PEDOT:PSS increases by 0.1 eV with FBI modification, resulting in Pb-Sn PSCs with 20.5% efficiency and an impressive V-OC of 0.843 V. Finally, we have successfully transferred our in situ buried interface modification strategy to fabricate blade-coated FA(0.6)MA(0.4)Pb(0.4)Sn(0.6)I(3) PSCs with 18.3% efficiency and an exceptionally high V-OC of 0.845 V.
引用
收藏
页码:39399 / 39407
页数:9
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