Blue Organic Long Persistent Luminescence: A UV/Violet‐Light‐Excitable and Green/Red‐Light‐Erasable Donor‐Sensitizer‐Acceptor Organic Afterglow System

W Wen Xia (State Key Laboratory of Organometallic Chemistry and Shanghai Hongkong Joint Laboratory in Chemical Synthesis Key Laboratory of Synthetic and Self‐Assembly Chemistry for Organic Functional Molecules Ningbo Zhongke Creation Center of New Materials Shanghai Institute of Organic Chemistry Chinese Academy of Sciences University of Chinese Academy of Sciences 345 Lingling Road Shanghai 200032 P.R. China) Z Zi Ye G Guoyi Wu H Honghong Yao H Hongxin Gao B Biao Xu Q Qianhui Chong (State Key Laboratory of Organometallic Chemistry and Shanghai Hongkong Joint Laboratory in Chemical Synthesis Key Laboratory of Synthetic and Self‐Assembly Chemistry for Organic Functional Molecules Ningbo Zhongke Creation Center of New Materials Shanghai Institute of Organic Chemistry Chinese Academy of Sciences University of Chinese Academy of Sciences 345 Lingling Road Shanghai 200032 P.R. China) K Kaka Zhang

Abstract

Abstract We pioneered a donor–sensitizer–acceptor three‐component system to devise organic long persistent luminescence (OLPL) materials, where the afterglow color is solely determined by sensitizer's emission color. Here we report two major breakthroughs in the field of OLPL: 1) tailored fabrication of pure‐blue OLPL materials and 2) a direct observation of OLPL erased by green/red lights. We rationally designed blue thermally activated delayed fluorescence (TADF) sensitizers by connecting biphenyl‐containing group with suitable HOMO and T 1 energy levels to difluoroboron β‐diketonate moiety based on the energy gap law and the El‐Sayed rule. The resultant donor–sensitizer–acceptor three‐component materials exhibit pure‐blue hour‐long OLPL afterglow with λ OLPL < 450 nm; such pure‐blue OLPL materials remain elusive in the reported studies. Mechanistic investigations confirm a unique charge‐separation‐induced OLPL pathway, involving electron transfer processes between donor, sensitizer, and acceptor. The OLPL materials are UV/visible‐light‐excitable. Remarkably, it is found that the OLPL emission can be erased by green or red light; the long‐lived excited TADF sensitizers can be pushed by green/red lights to higher excited states, followed by fast nonradiative deactivation, enabling optical erasure. This unprecedented optical write–erase functionality, coupled with hour‐long OLPL duration, would offer promising opportunities for rewritable photonic storage, encryption, and dynamic labeling applications.

Article Details

Volume / Issue Vol. 64, Issue 48
Published November 24, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

W

Wen Xia

State Key Laboratory of Organometallic Chemistry and Shanghai Hongkong Joint Laboratory in Chemical Synthesis Key Laboratory of Synthetic and Self‐Assembly Chemistry for Organic Functional Molecules Ningbo Zhongke Creation Center of New Materials Shanghai Institute of Organic Chemistry Chinese Academy of Sciences University of Chinese Academy of Sciences 345 Lingling Road Shanghai 200032 P.R. China

Z

Zi Ye

G

Guoyi Wu

H

Honghong Yao

H

Hongxin Gao

B

Biao Xu

Q

Qianhui Chong

State Key Laboratory of Organometallic Chemistry and Shanghai Hongkong Joint Laboratory in Chemical Synthesis Key Laboratory of Synthetic and Self‐Assembly Chemistry for Organic Functional Molecules Ningbo Zhongke Creation Center of New Materials Shanghai Institute of Organic Chemistry Chinese Academy of Sciences University of Chinese Academy of Sciences 345 Lingling Road Shanghai 200032 P.R. China

K

Kaka Zhang