Host‐Dependent Tunable Phosphorescence Based on Aromatic Heterocyclic Derivatives: Highly Efficient and Photo‐Activated Ultralong Organic Phosphorescence

H Huanyu Yang Y Yuefei Wang (CAS Key Laboratory of Nano-Bio Interface, Jiangsu Key Laboratory of Organoid Engineering and Precision Medicine, Division of Nanobiomedicine and i-Lab) Y Ying Wang Z Zaiyong Zhang H Huili Ma (State Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies)) Y Yoshihiro Yamauchi (National Institute for Material Science (NIMS) 1‐2‐1 Sengen Tsukuba Ibaraki 305‐0047 Japan) K Kejia Ling (Strait Institute of Flexible Electronics (SIFE Future Technologies) Fujian Key Laboratory of Flexible Electronics Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE) Fuzhou Fujian 350117 China) Y Yi Zhao (State Key Laboratory of Quantum Functional Materials, School of Physical Science and Technology) S Suzhi Cai Z Zhongfu An (State Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies)) W Wei Huang

Abstract

Abstract Achieving high phosphorescence efficiency and photo‐activated ultralong organic phosphorescence (UOP) based on the same molecule remains a formidable challenge. Here, a concise strategy is proposed to obtain highly efficient and photo‐activated RTP by doping aromatic heterocyclic derivatives into different polymers. Aromatic heterocyclic derivatives are doped into PAM, PVA, or PAA polymers to produce high phosphorescence efficiency. Impressively, the highest phosphorescence quantum yield can reach up to 66.2% at room temperature, which can be attributed to isolating the chromophore to reduce the excimer and the rigid environment from the polymer to restrict the non‐radiative transitions. In addition, phosphorescence emission color can be tailored from green to deep blue by varying the guests. After aromatic heterocyclic derivatives are doped into PDMA or PVP, the phosphorescence lifetime is prolonged from 1.2 to 578.6 ms. These polymers are successfully applied to multicolor displays and high‐level information storage. This work provides a reasonable strategy to develop highly efficient and photo‐activated RTP materials based on the same molecule.

Article Details

Volume / Issue Vol. 37, Issue 42
Published October 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

H

Huanyu Yang

Y

Yuefei Wang

CAS Key Laboratory of Nano-Bio Interface, Jiangsu Key Laboratory of Organoid Engineering and Precision Medicine, Division of Nanobiomedicine and i-Lab

Y

Ying Wang

Z

Zaiyong Zhang

H

Huili Ma

State Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies)

Y

Yoshihiro Yamauchi

National Institute for Material Science (NIMS) 1‐2‐1 Sengen Tsukuba Ibaraki 305‐0047 Japan

K

Kejia Ling

Strait Institute of Flexible Electronics (SIFE Future Technologies) Fujian Key Laboratory of Flexible Electronics Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE) Fuzhou Fujian 350117 China

Y

Yi Zhao

State Key Laboratory of Quantum Functional Materials, School of Physical Science and Technology

S

Suzhi Cai

Z

Zhongfu An

State Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies)

W

Wei Huang