Evidence map›Paper›PMID 42303636›Full record

ArticleNature communications2026

Dynamic hydroxyl mediated charge buffering stabilizes high valence ruthenium edge sites for acidic water oxidation.

Tianqing Yan, Kang Xue, Shishi Zhang, Huayang Wang, Zhen-Feng Huang, Minhua Ai, Ruijie Gao, Chengxiang Shi, Wanliang Mi, Xiangwen Zhang and 2 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Nature communications, 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
–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

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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

12 authors.

Tianqing Yan *Key Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Kang Xue *Key Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Shishi ZhangKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Huayang WangKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Zhen-Feng HuangKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China. zfhuang@tju.edu.cn.ORCID http://orcid.org/0000-0001-9656-9186
Minhua AiKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Ruijie GaoKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Chengxiang ShiKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Wanliang MiBeijing Hydrogen E Energy Science & Technology Co., Ltd, Beijing, China.
Xiangwen ZhangKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Lun PanKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China. panlun76@tju.edu.cn.ORCID http://orcid.org/0000-0002-3083-4693
Ji-Jun ZouKey Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China. jj_zou@tju.edu.cn.ORCID http://orcid.org/0000-0002-9126-1251

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22121004National Natural Science Foundation of China (National Science Foundation of China) 22222808National Natural Science Foundation of China (National Science Foundation of China) 22278307
6 · The paper itself

Abstract

High valence metal species are essential for driving electrocatalytic acidic water oxidation, but suffer from intrinsic thermodynamic instability. This activity-stability paradox is particularly severe for ruthenium-based catalysts, where highly active Ru(>IV) species are also precursors for rapid dissolution. Here we show that a cooperative host-guest architecture circumvents this trade-off through dynamic, hydroxyl-mediated charge buffering. By anchoring isolated ruthenium atoms at β-MnO

Identifiers

PMID42303636
PMCPMC13434782

What OpenQuestion holds

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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.