Evidence map›Paper›PMID 41339317›Full record

ArticleNature communications2025

Mechanically-robust and humidity-tunable self-destructive polymers enabled by hydrogen-bond nanoconfinement.

Hualiang Xu, Tiantai Yang, Yuan Lei, Xiaowei Fu, Zhimeng Liu, Shanshan Li, Liang Jiang, Jingxin Lei

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. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Hualiang XuState Key Laboratory of Advanced Polymer Materials, Polymer Research Institute of Sichuan University, Chengdu, 610065, Sichuan, China.ORCID http://orcid.org/0000-0001-8235-1653
Tiantai YangState Key Laboratory of Advanced Polymer Materials, Polymer Research Institute of Sichuan University, Chengdu, 610065, Sichuan, China.
Yuan LeiState Key Laboratory of Advanced Polymer Materials, Polymer Research Institute of Sichuan University, Chengdu, 610065, Sichuan, China.
Xiaowei FuState Key Laboratory of Advanced Polymer Materials, Polymer Research Institute of Sichuan University, Chengdu, 610065, Sichuan, China.
Zhimeng LiuSchool of Chemical Engineering, Sichuan University, Chengdu, 610065, Sichuan, China.
Shanshan LiKey Laboratory of Green Chemistry and Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu, 610064, Sichuan, China.
Liang JiangState Key Laboratory of Advanced Polymer Materials, Polymer Research Institute of Sichuan University, Chengdu, 610065, Sichuan, China. liangjiang@scu.edu.cn.ORCID http://orcid.org/0000-0003-1305-1926
Jingxin LeiState Key Laboratory of Advanced Polymer Materials, Polymer Research Institute of Sichuan University, Chengdu, 610065, Sichuan, China. jxlei@scu.edu.cn.ORCID http://orcid.org/0000-0003-0041-7554

Funding

National Natural Science Foundation of China (National Science Foundation of China) No. 52403274
6 · The paper itself

Abstract

Conventional materials typically maintain a stable solid state under specific application conditions. However, materials that combine high mechanical strength with reversible switching states are highly desirable for advanced technologies. Here, we present hydrogen-bond nanoconfined self-destructive polymers (HNSPs) that have robust mechanics and reversible solid-fluid switching capability at 25 °C. Upon exposure to moisture, HNSPs spontaneously transition from solid to fluid, with humidity-tunable switching rates. HNSPs with weight ratios (Rm) of 1.7 is 1.69 times higher self-destructive rate than those with Rm of 2.1, and at 90% relative humidity (RH), Rm=2.0 samples exhibit an 804.27% higher self-destructive efficiency than at 60% RH. Heating can reverse the fluid back to a solid, enabling reversible, humidity-programmable behavior. Mechanistically, large ordered hydrogen-bond clusters, reduced chain entanglement, and abundant hydrophilic groups collectively facilitate switching. This work provides a simple yet versatile strategy for designing robust, switchable self-destructive polymers, broadening their potential in next-generation devices.

Identifiers

PMID41339317
PMCPMC12706017

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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.