Affiliation:
1. Department of Applied Chemistry Yuncheng University Yuncheng 044000 P. R. China
2. Department of Nursing First Hospital of Shanxi Medical University Taiyuan 030001 P. R. China
3. Key Laboratory of Smart Grid of Education Ministry Tianjin University Tianjin 300072 P. R. China
4. School of Chemistry Key Laboratory of Bio‐inspired Smart Interfacial Science and Technology of Ministry of Education Beijing Advanced Innovation Center for Biomedical Engineering Beihang University Beijing 100191 P. R. China
Abstract
AbstractPerovskites with superior photophysical properties and simple solution processing are widely applied in solar cells, light‐emitting diodes, photodetectors, and lasers. However, the target of high‐performance multifunctional perovskite optoelectronics is hampered by their intrinsic properties, such as the undesired crystallization rate, ease of ion migration, poor stability, and high brittleness. A perovskite–polymer matrix, including a perovskite–polymer composite and a polymer–perovskite–polymer heterostructure, is adopted to handle the above issues. This review starts with the categorized polymer addition methods and the relevant polymer distribution for a perovskite–polymer matrix. In addition, the high performance originating from the controlled crystallization, stress regulation, inhibited ion migration, defect passivation, reduced interfacial recombination, and multifunctions from the enhanced stability, mechanical robustness, self‐healing ability, controllable dimension, and novel optical properties are then summarized. Meanwhile, the working mechanisms of a perovskite–polymer matrix in perovskite optoelectronics are also discussed. Finally, promising guidelines and proposals are provided to promote the commercialization of high‐performance multifunctional perovskite optoelectronics.
Funder
National Natural Science Foundation of China
Shanxi Scholarship Council of China
Subject
Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献