Evidence map›Paper›PMID 42441733›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Non-Fluorinated Functional Polyolefin for Puncture-Resistant and Self-Healable Proton Exchange Membranes of Fuel Cells.

Yue Liu, Lu Liu, Shuyu Zheng, Yiren Gao, Panchao Yin, Zhaomin Hou, Haobing Wang

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

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

7 authors.

Yue LiuAdvanced Institute for Soft Matter Science and Technology (AISMST), School of Emergent Soft Matter, State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, China.
Lu LiuAdvanced Institute for Soft Matter Science and Technology (AISMST), School of Emergent Soft Matter, State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, China.
Shuyu ZhengAdvanced Institute for Soft Matter Science and Technology (AISMST), School of Emergent Soft Matter, State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, China.
Yiren GaoAdvanced Institute for Soft Matter Science and Technology (AISMST), School of Emergent Soft Matter, State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, China.
Panchao YinAdvanced Institute for Soft Matter Science and Technology (AISMST), School of Emergent Soft Matter, State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, China.ORCID https://orcid.org/0000-0003-2902-8376
Zhaomin HouAdvanced Catalysis Research Group, RIKEN Center for Sustainable Resource Science, Saitama, Japan.ORCID https://orcid.org/0000-0003-2841-5120
Haobing WangAdvanced Institute for Soft Matter Science and Technology (AISMST), School of Emergent Soft Matter, State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, China.ORCID https://orcid.org/0000-0002-9104-1726

Funding

Guangdong Basic and Applied Basic Research Foundation 2024A1515011330Introduced Innovative R&D Team of Guangdong 2021ZT09L392National Key R&D Program of China 2025ZD0614400National Natural Science Foundation of China 22171091Science and Technology Program of Guangzhou 2024D03J0003
6 · The paper itself

Abstract

The development of puncture-resistant and self-healing proton exchange membranes (PEMs) is vital for enhancing fuel cells' (FCs) durability and safety; however, it remains a formidable challenge. Herein, we report a non-fluorinated polyolefin-based PEM that integrates autonomous self-healing, puncture resistance, high gas barrier, and exceptional overall durability in FC applications. The polymers are prepared through rare-earth-catalyzed selective polymerization of isoprene, partial hydrogenation, thiol-ene click chemistry, and oxidation, yielding a sulfonic acid-functionalized polyolefin. The main chain structure of polymers features rigid poly(3-methyl-1-butene) segments-derived from 3,4-polyisoprene units-and soft ethylene-alt-propylene sequences-originating from cis-1,4-polyisoprene units. The nanoscale microphase separation between these hard and soft segments provides exceptional mechanical robustness and self-healing capability, while the aggregation of sulfonic acid groups creates efficient proton transport pathways. The resulting membrane achieves high through-plane proton conductivity of 1.0 × 10

Indexed as

non‐fluorinatedpolyolefinproton exchange membranepuncture‐resistantself‐healing

Identifiers

PMID42441733
PMCPMC13573035

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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.