Evidence map›Paper›PMID 41184245›Full record

ArticleNature communications2025

Full-color programmable high temperature afterglow polymers based on single-molecule emitters.

Zhuoran Xu, Yufeng Huang, Siyu Sun, Liangwei Ma, Bingbing Ding, He Tian, Xiang Ma

Abstract read
PubMed Full text at PMC Publisher
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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

7 authors.

Zhuoran Xu *Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, PR China.
Yufeng Huang *Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, PR China.
Siyu SunKey Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, PR China. sunsiyu95@163.com.ORCID http://orcid.org/0000-0002-4642-7902
Liangwei MaKey Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, PR China.ORCID http://orcid.org/0000-0001-9435-7374
Bingbing DingKey Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, PR China.ORCID http://orcid.org/0000-0002-8821-143X
He TianKey Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, PR China.ORCID http://orcid.org/0000-0003-3547-7485
Xiang MaKey Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, PR China. maxiang@ecust.edu.cn.ORCID http://orcid.org/0000-0002-8679-4491

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22125803, T2488302, and 22020102006
6 · The paper itself

Abstract

High-temperature afterglow organic amorphous materials expand the operational temperature beyond traditional room-temperature phosphorescent materials, broadening their potential applications. However, achieving tunable high-temperature afterglow from a single luminescent molecule remains a formidable challenge. Here, we employ host-guest anchoring coupled with single-bond rotors to achieve effective phosphorescence and tunable afterglow at high temperature simultaneously. The material demonstrates a wavelength-tunable afterglow: during heating (298 K to 473 K), the chromaticity coordinate shifts from (0.24, 0.47) to (0.18, 0.20) and the lifetime from 836 ms to 6.34 ms. The theoretical investigations reveal that the excited-state conformation of phosphors undergoes a temperature-dependent transformation, inducing the wavelength-tunable high-temperature afterglow phenomenon. This work offers a strategy for designing tunable high-temperature afterglow-emitting amorphous polymers, advancing the development of organic phosphorescent materials capable of delivering tunable high-temperature afterglow emissions.

Identifiers

PMID41184245
PMCPMC12583763

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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.