Unveiling the Complex Evolution in Mixed Br–Cl Perovskite Precursors for High‐Efficiency Deep‐Blue Light‐Emitting Diodes

Author:

Jia Yongheng1,Li Ruichen23,Zhou Yang1,Zhao Shenghe1,Yu Hui1,Wang Jianpu4,Lin Zhenyang23,Su Haibin23,Zhao Ni1ORCID

Affiliation:

1. Department of Electronic Engineering The Chinese University of Hong Kong New Territories Hong Kong

2. Department of Chemistry The Hong Kong University of Science and Technology Kowloon Hong Kong

3. Department of Function Hub The Hong Kong University of Science and Technology (Guangzhou) No. 1 Duxue Road Nansha District Guangzhou 511458 China

4. Key Laboratory of Flexible Electronics and Institute of Advanced Materials Nanjing Tech University Nanjing 211816 China

Abstract

Perovskite light‐emitting diodes (PeLEDs) based on 3D mixed Br‐Cl compositions have shown good color stability and efficiency in the sky‐blue color range. However, when the Cl/Br ratio increases to reach deep‐blue emission, the performance of the PeLEDs decreases drastically, with the external quantum efficiency (EQE) typically below 1%. Such performance decay is due largely to the poor morphology of the emissive layer. Herein, theoretical and experimental approach is combined to investigate the evolution of solvated lead complexes in the precursor solution of mixed Br–Cl perovskites. It is found that the energetically favorable exchange of halide ions in the lead complexes drives the precipitation of CsCl, leading to extremely low precursor solubility at high Cl/Br ratios and consequently poor perovskite film coverage. Based on the findings, a metastable dissolution strategy for perovskite film preparation is proposed and deep‐blue PeLEDs with a record high EQE of 4% in 3D‐based PeLEDs and excellent spectral stability is achieved.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Earth and Planetary Sciences,General Environmental Science

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