Evidence map›Paper›PMID 41093857›Full record

ArticleNature communications2025

Radical-enhanced photo-activated ultralong organic phosphorescence.

Yuefei Wang, Zaiyong Zhang, Huanyu Yang, Shunjie Li, Xiaokang Yao, Huili Ma, Shengchen Yang, Suzhi Cai, Zhongfu An, Wei Huang

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Yuefei WangInstitute of Flexible Electronics (SIFE, Future Technologies), Fujian Key Laboratory of Flexible Electronics, Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE), Fuzhou, Fujian, China.
Zaiyong ZhangPharmaceutical Analytical & Solid-State Chemistry Research Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Huanyu YangInstitute of Flexible Electronics (SIFE, Future Technologies), Fujian Key Laboratory of Flexible Electronics, Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE), Fuzhou, Fujian, China.
Shunjie LiInstitute of Flexible Electronics (SIFE, Future Technologies), Fujian Key Laboratory of Flexible Electronics, Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE), Fuzhou, Fujian, China.
Xiaokang YaoState Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies), Nanjing Tech University (NanjingTech), Nanjing, 211816, China.
Huili MaState Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies), Nanjing Tech University (NanjingTech), Nanjing, 211816, China.ORCID http://orcid.org/0000-0003-0332-2999
Shengchen YangDepartment of Materials Chemistry, Huzhou University, Huzhou, China.
Suzhi CaiInstitute of Flexible Electronics (SIFE, Future Technologies), Fujian Key Laboratory of Flexible Electronics, Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE), Fuzhou, Fujian, China. ifeszhcai@fjnu.edu.cn.
Zhongfu AnState Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies), Nanjing Tech University (NanjingTech), Nanjing, 211816, China. iamzfan@njtech.edu.cn.ORCID http://orcid.org/0000-0002-6522-2654
Wei HuangInstitute of Flexible Electronics (SIFE, Future Technologies), Fujian Key Laboratory of Flexible Electronics, Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE), Fuzhou, Fujian, China. vc@nwpu.edu.cn.ORCID http://orcid.org/0000-0001-7004-6408

Funding

National Natural Science Foundation of China (National Science Foundation of China) 62288102
6 · The paper itself

Abstract

Stimuli-responsive ultralong room temperature phosphorescence materials have attracted great attention due to their great potential in a wide variety of advanced applications. Photo-activated phosphorescence lifetime and photo-activation time are constant and highly dependent on the inherent properties of the materials. It is a great challenge to manipulate them. Herein, we propose a facile strategy to prolong photo-activated phosphorescence emission and shorten photo-activation time by consuming the oxygen in polymer matrix through UV irradiation and radical coupling. The phosphorescence lifetime increases from 0.08 ms to 360 ms after 30-minute UV irradiation. When the guest molecules in solution are photoactivated and subsequently doped into the polymer, the photoactivated phosphorescence lifetime can reach up to 621 ms after just 5-second UV irradiation. This enhancement is attributed to the ability of triarylphosphine radical cations to capture oxygen in polymer through radical coupling. Furthermore, these polymer films have been successfully applied in information storage, programmable afterglow tags, and anti-counterfeiting. This work overcomes the intrinsic limitations of materials and paves the way for regulating photoactivated phosphorescence lifetime and photoactivation time.

Identifiers

PMID41093857
PMCPMC12528461

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.