Multifunctional Ionic‐Ligand Regulated High‐Quality γ‐CsPbI3 Thin Films for Efficient and Bright Deep‐Red Light‐Emitting Diodes

Author:

Ru Xue‐Chen1,Zhu Bai‐Sheng12,Ma Zhen‐Yu12,Hao Jing‐Ming12,Ding Guan‐Jie12,Song Yong‐Hui12,Feng Li‐Zhe12,Song Kuang‐Hui12,Li Lian‐Yue12,Yao Hong‐Bin12ORCID

Affiliation:

1. Hefei National Research Center for Physical Sciences at the Microscale University of Science and Technology of China Hefei Anhui 230026 China

2. Department of Applied Chemistry University of Science and Technology of China Hefei Anhui 230026 China

Abstract

AbstractAll‐inorganic CsPbI3 perovskite semiconductor is attractive for deep‐red light‐emitting diodes (LEDs) because of its high photoluminescence, good thermal stability, excellent charge transport, and solution processability. However, the metastable phase of optically active CsPbI3 hinders the fabrication of efficient and bright deep‐red LEDs. Herein, a multifunctional ionic ligand regulation strategy using (2‐hydroxy‐5‐methylphenyl) triphenyl‐phosphonium iodide and 3‐(N, N‐dimethyloctylammonio) propanesulfonate is reported to regulate the optically active CsPbI3 crystallization and thus obtain high‐quality γ‐CsPbI3 thin films. The high crystallinity and preferential orientation of γ‐CsPbI3 arise from the strong bonding between the ionic ligands and ionic lead halide clusters. The obtained γ‐CsPbI3 thin films also possess suppressed defect densities, high luminescence, and high stability. Using this high‐quality thin film, an efficient and bright deep‐red LED with a peak external quantum efficiency of 13.34% and a maximum luminance of 2110 cd m−2 is successfully fabricated. The operational lifetime of the fabricated LED (time to half of the initial brightness, T50) reaches up to 40 min under a high current density of 50 mA cm−2 (corresponding to the initial brightness of 200 cd m−2).

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

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