Halide Substituted Ammonium Salt Optimized Buried Interface for Efficient and Stable Flexible Perovskite Solar Cells

Author:

An Ziqi1,Zhu Yanqing1,Luo Gan1,Hou Peiran1,Hu Min2,Li Wangnan3,Huang Fuzhi4,Cheng Yi‐Bing4,Park Hyesung56,Lu Jianfeng1ORCID

Affiliation:

1. State Key Laboratory of Silicate Materials for Architectures Wuhan University of Technology Wuhan 430070 China

2. School of Electronic and Electrical Engineering Hubei Province Engineering Research Center for Intelligent Micro‐Nano Medical Equipment and Key Technologies Wuhan Textile University Wuhan 430200 China

3. Hubei Key Laboratory of Low Dimensional Optoelectronic Material and Devices Hubei University of Arts and Science Xiangyang 441053 China

4. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China

5. KU‐KIST Graduate School of Converging Science and Technology Korea University 145 Anam‐ro, Seongbuk‐gu Seoul 02841 Republic of Korea

6. Department of Integrative Energy Engineering Korea University 145 Anam‐ro, Seongbuk‐gu Seoul 02841 Republic of Korea

Abstract

AbstractLow‐temperature solution processing of the perovskite layer enables the fabrication of flexible devices. However, the performance of flexible perovskite solar cells (f‐PSCs) lags far behind their rigid counterpart in terms of efficiency and stability. Emerging evidence demonstrates that the quality of the buried interface between perovskite and transporting layer underneath is the key point. Herein, a class of novel halide substituted ammonium salts, i.e., n‐bromophenethylammonium (n‐Br‐PEAX, n = 2 or 4, X = Cl or Br) are designed and synthesized to modify the buried interface as well as the perovskite crystallization of f‐PSCs. It is found that the ammonium salt with rational design molecular structure can modify the crystallization speed of perovskite, leading to the formation of a compact and uniform morphology without nanovoids at the interface. As a result, the efficiency of f‐PSCs is improved from 15.4% to 20.2%. Moreover, the modified devices without encapsulation retain 86% of their initial performance after 1000 h of aging at ambient conditions and 87% after 290 h of continuous operation.

Funder

National Natural Science Foundation of China

Shanxi Provincial Key Research and Development Project

Natural Science Foundation of Hubei Province

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing

National Research Foundation of Korea

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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