Homogenizing The Low‐Dimensional Phases for Stable 2D‐3D Tin Perovskite Solar Cells

Author:

Kang Ziyong1,Wang Kun2,Zhang Lu3,Yang Yang1,Wu Jiandong1,Tong Yu1,Yan Peng1,Chen Yali1,Qi Heng1,Sun Kun4,Müller‐Buschbaum Peter4,Zhang Xuewen5,Shang Jingzhi5,Wang Hongqiang1ORCID

Affiliation:

1. State Key Laboratory of Solidification Processing Center for Nano Energy Materials School of Materials Science and Engineering Northwestern Polytechnical University Xi'an 710072 China

2. School of microelectronics Northwestern Polytechnical University Xi'an 710072 China

3. Key Laboratory of Applied Surface and Colloid Chemistry Ministry of Education Shaanxi Key Laboratory for Advanced Energy Devices Shaanxi Engineering Lab for Advanced Energy Technology School of Materials Science and Engineering Shaanxi Normal University Xi'an 710119 P. R. China

4. Chair for Functional Materials Department of Physics TUM School of Natural Sciences Technical University of Munich James‐Franck‐Str. 1 85748 Garching Germany

5. Institute of Flexible Electronics Northwestern Polytechnical University Xi'an 710129 China

Abstract

Abstract2D‐3D tin‐based perovskites are considered as promising candidates for achieving efficient lead‐free perovskite solar cells (PSCs). However, the existence of multiple low‐dimensional phases formed during the film preparation hinders the efficient transport of charge carriers. In addition, the non‐homogeneous distribution of low‐dimensional phases leads to lattice distortion and increases the defect density, which are undesirable for the stability of tin‐based PSCs. Here, mixed spacer cations [diethylamine (DEA+) and phenethylamine (PEA+)] are introduced into tin perovskite films to modulate the distribution of the 2D phases. It is found that compared to the film with only PEA+, the combination of DEA+ and PEA+ favors the formation of homogeneous low‐dimensional perovskite phases with three octahedral monolayers (n = 3), especially near the bottom interface between perovskite and hole transport layer. The homogenization of 2D phases help improve the film quality with reduced lattice distortion and released strain. With these merits, the tin PSC shows significantly improved stability with 94% of its initial efficiency retained after storing in a nitrogen atmosphere for over 4600 h, and over 80% efficiency maintained after continuous illumination for 400 h.

Funder

Natural Science Basic Research Program of Shaanxi Province

Fundamental Research Funds for the Central Universities

China Scholarship Council

Publisher

Wiley

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