Strain Regulation of Mixed‐Halide Perovskites Enables High‐Performance Wide‐Bandgap Photovoltaics

Author:

Li Xinhao1,Li Yifan1,Feng Yanxing23,Qi Jiahui1,Shen Jinliang1,Shi Guodong4,Yang Shaopeng15,Yuan Mingjian2,He Tingwei15ORCID

Affiliation:

1. Hebei Key Laboratory of Optic‐electronic Information and Materials College of Physics Science and Technology Hebei University Baoding 071002 China

2. Department of Chemistry Nankai University Tianjin 300071 China

3. School of Materials Science and Engineering School of Chemistry and Chemical Engineering Henan Normal University Xinxiang 453007 China

4. College of Science Henan University of Technology Zhengzhou 450001 China

5. Province‐Ministry Co‐construction Collaborative Innovation Center of Hebei Photovoltaic Technology Hebei University Baoding 071002 China

Abstract

AbstractWide‐bandgap mixed‐halogen perovskite materials are widely used as top cells in tandem solar cells. However, serious open‐circuit voltage (Voc) loss restricts the power conversion efficiency (PCE) of wide‐bandgap perovskite solar cells (PSCs). Herein, it is shown that the resulting methylammonium vacancies induce lattice distortion in methylammonium chloride‐assisted perovskite film, resulting in an inhomogeneous halogen distribution and low Voc. Thus, a lattice strain regulation strategy is reported to fabricate high‐performance wide‐bandgap PSCs. Rubidium (Rb) cations are introduced to fill the A‐site vacancy caused by the methylammonium volatilization, which alleviates shrinkage strain of the perovskite crystal. The reduced lattice distortion and increased halide ion migration barrier result in a homogeneous mixed‐halide perovskite film. Due to improved carrier transport and suppressed nonradiative recombination, the Rb‐treated wide‐bandgap PSC (1.68 eV) achieves an excellent PCE of 21.72%, accompanied by a high Voc of 1.22 V. The resulting device maintains more than 90% of its initial PCE after 1500 h under 1‐sun illumination conditions.

Publisher

Wiley

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