Tribenzyl Organic Cations Carried Multidentate X‐Type Lewis Soft Base for High‐Performance Foldable Perovskite Light‐Emitting Diodes

B Benzheng Lyu (School of Chemistry and Chemical Engineering Ministry of Education Key Laboratory of Special Functional Aggregated Materials Shandong Key Laboratory of Advanced Organosilicon Materials and Technologies Shandong University Jinan China) D Dongyu Li (Department of Molecular Genetics, University of Texas Southwestern Medical Center) C Chengxuan Ke (Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen 518055 P. R. China) H Haoquan Liang (Institute of Fundamental and Frontier Sciences University of Electronic Science and Technology of China Chengdu 611731 P. R. China) J Jiayun Sun Q Qi Xiong (Department of Materials Science and Engineering) J John Jinwook Kim (Department of Electrical and Electronic Engineering The University of Hong Kong Pokfulam Road Hong Kong 999077 China) Y Yanning Zhang (State Key Laboratory of Regional Environment and Sustainability, School of Environment, Tsinghua University) G Guangfu Luo (Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China) W Wallace C. H. Choy

Abstract

Abstract Lead‐halide perovskite nanocrystals (PNCs) exhibit significant potential for advancing foldable perovskite light‐emitting diodes ( F ‐PLEDs) due to their discrete crystalline morphology, bright emission across an extensive color gamut, and remarkable color purity; however, their progression remains in the early stages with the concerns of inadequate performance and mechanical instability. This study proposes a ligand strategy employing tribenzyl organic cation (tribenzylamine, TBA) carried multidentate X‐type Lewis soft base (sodium acid pyrophosphate, SAPP) to address the challenges above simultaneously. Specifically, the use of multibranched aromatic ligands considerably improved the adhesion force between PNCs and adjacent layers, enhancing mechanical stability during folding, while the control sample shows deleterious cracks. Additionally, TBA‐SAPP ligands effectively eliminate the defects in PNC film, yielding exceptional photoluminescence properties with a near‐unity quantum yield. Consequently, the multifunctional ligands improved F ‐PLEDs to achieve a record‐high external quantum efficiency (EQE) of 16.2% compared to the previously reported pure‐red flexible PLEDs and display substantially improved spectral and operational stability. Equally important, these devices demonstrate robust mechanical properties, enduring a small folding radius of 1 mm for 5000 cycles. This ligand strategy is anticipated to inspire relevant research in PNCs and promote the realization of highly efficient and mechanically stable F ‐PLEDs.

Article Details

Volume / Issue Vol. 37, Issue 25
Published June 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

B

Benzheng Lyu

School of Chemistry and Chemical Engineering Ministry of Education Key Laboratory of Special Functional Aggregated Materials Shandong Key Laboratory of Advanced Organosilicon Materials and Technologies Shandong University Jinan China

D

Dongyu Li

Department of Molecular Genetics, University of Texas Southwestern Medical Center

C

Chengxuan Ke

Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen 518055 P. R. China

H

Haoquan Liang

Institute of Fundamental and Frontier Sciences University of Electronic Science and Technology of China Chengdu 611731 P. R. China

J

Jiayun Sun

Q

Qi Xiong

Department of Materials Science and Engineering

J

John Jinwook Kim

Department of Electrical and Electronic Engineering The University of Hong Kong Pokfulam Road Hong Kong 999077 China

Y

Yanning Zhang

State Key Laboratory of Regional Environment and Sustainability, School of Environment, Tsinghua University

G

Guangfu Luo

Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China

W

Wallace C. H. Choy