Molecule Anchoring Strategy Promotes Vertically Homogeneous Crystallization and Aligned Interfaces for Efficient Pb–Sn Perovskite Solar Cells and Tandem Device

Author:

Xing Gang1,Li Changbo1,Gao Weiyin12,Yang Jianxiong1,Zhao Xiaojia1,Wang Jinpei3,Ran Xueqin3,Chao Lingfeng3,Huang Hai2,Zhou Yipeng1,Chen Yonghua3,Wu Zhongbin1,Ran Chenxin145,Huang Wei13ORCID

Affiliation:

1. Frontiers Science Center for Flexible Electronics Xi'an Institute of Flexible Electronics (IFE) and Northwestern Polytechnical University Xi'an 710072 China

2. College of New Energy Xi'an Shiyou University Xi'an 710065 China

3. Key Laboratory of Flexible Electronics (KLOFE) & Institution of Advanced Materials (IAM) Nanjing Tech University (NanjingTech) Nanjing Jiangsu 211816 P. R. China

4. Research & Development Institute of Northwestern Polytechnical University in Shenzhen Shenzhen 518063 China

5. Chongqing Innovation Center Northwestern Polytechnical University Chongqing 401135 China

Abstract

AbstractNarrow‐bandgap (NBG) Pb–Sn perovskites are ideal candidates as rear subcell in all‐perovskite tandem solar cells. Because Pb–Sn perovskites contain multiple components, the rational regulation of vertical structure and both interfaces of the film is primarily crucial to achieve high‐performing NBG perovskite solar cells (PSCs). Herein, a molecule anchoring strategy is developed to in situ construct Cs0.1MA0.3FA0.6Pb0.5Sn0.5I3 perovskite film with vertically aligned crystals and optimized interfaces. Specifically, l‐alanine methyl ester is developed as an anchoring additive to induce the vertical crystal growth, while PEA2PbI3SCN film is introduced to promote the homogeneous crystallization at the buried interface via SCN− anchoring with cations. Further ethylenediamine dihalides (EDA(I/Cl)2) post‐treatment leads to the gradient energy level alignment on the film surface. Pb–Sn PSCs based on such film show efficient charge transport and extraction, producing a champion power conversion efficiency (PCE) of 22.3% with an impressive fill factor of 82.14%. Notably, combining with semitransparent 1.78 eV wide‐bandgap PSCs, the four‐terminal all‐perovskite tandem device achieves a PCE of 27.1%. This work opens up a new pathway to boost the performance of Pb–Sn PSCs and their tandem devices.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

China Postdoctoral Science Foundation

Fundamental Research Funds for the Central Universities

Basic and Applied Basic Research Foundation of Guangdong Province

Publisher

Wiley

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