High-Performance Lead-Free Solar Cells Based on Tin-Halide Perovskite Thin Films Functionalized by a Divalent Organic

被引:99
作者
Chen, Min [1 ]
Dong, Qingshun [1 ,2 ]
Eickemeyer, Felix T. [3 ]
Liu, Yuhang [3 ]
Dai, Zhenghong [1 ]
Carl, Alexander D. [4 ]
Bahrami, Behzad [5 ]
Chowdhury, Ashraful H. [5 ]
Grimm, Ronald L. [4 ]
Shi, Yantao [2 ]
Qiao, Qiquan [5 ]
Zakeeruddin, Shaik Mohammed [3 ]
Gratzel, Michael [3 ]
Padture, Nitin P. [1 ]
机构
[1] Brown Univ, Sch Engn, Providence, RI 02912 USA
[2] Dalian Univ Technol, Dept Chem, State Key Lab Fine Chem, Sch Chem Engn, Dalian 116024, Peoples R China
[3] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, Lab Photon & Interfaces, CH-1052 Lausanne, Switzerland
[4] Worcester Polytech Inst, Dept Chem & Biochem, Worcester, MA 01609 USA
[5] South Dakota State Univ, Dept Elect Engn & Comp Sci, Brookings, SD 57007 USA
基金
欧盟地平线“2020”; 瑞士国家科学基金会; 中国博士后科学基金; 中国国家自然科学基金; 美国国家科学基金会;
关键词
PHOTOLUMINESCENCE; EFFICIENCY;
D O I
10.1021/acsenergylett.0c00888
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Tin-based halide perovskite solar cells (PSCs) hold the most promise among lead-free PSCs, but they are plagued with inadequate environmental stability and power-conversion efficiency (PCE). Here we demonstrate that the optimum incorporation of a bulky divalent organic cation, 4-(aminomethyl)- piperidinium (4AMP), in FASnI(3) thin films improves stability, optoelectronic properties, and PSC performance. The optimized PSC yields a maximum PCE of 10.9% and good 500-h operational stability under continuous illumination. This is attributed to the unique thin-film structure, where the strong ionic bonding afforded by divalent 4AMP may provide near-full-coverage functionalization (encapsulation) of FASnI(3) grain surfaces and grain boundaries, retarding O-2/H2O ingression and mitigating Sn-defects for reduced photocarrier nonradiative recombination.
引用
收藏
页码:2223 / 2230
页数:8
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