Evidence map›Paper›PMID 39984483›Full record

ArticleNature communications2025

Kinetic cation effect in alkaline hydrogen electrocatalysis and double layer proton transfer.

Peng Li, Ya-Ling Jiang, Yana Men, Yu-Zhou Jiao, Shengli Chen

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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  4. Review
  5. Study on the Reaction Mechanism of RuOAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Article
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  10. Article
  11. Dynamic Interfacial Modulation in Pt@Ga Liquid Metal Systems.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  12. Article
  13. Article
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  16. 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

5 authors.

Peng LiHubei Key Laboratory of Electrochemical Power Sources, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, China.
Ya-Ling JiangHubei Key Laboratory of Electrochemical Power Sources, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, China.
Yana MenHubei Key Laboratory of Electrochemical Power Sources, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, China.
Yu-Zhou JiaoHubei Key Laboratory of Electrochemical Power Sources, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, China.
Shengli ChenHubei Key Laboratory of Electrochemical Power Sources, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, China. slchen@whu.edu.cn.ORCID http://orcid.org/0000-0001-7448-8860

Funding

National Natural Science Foundation of China (National Science Foundation of China) 21832004National Natural Science Foundation of China (National Science Foundation of China) 22202156National Natural Science Foundation of China (National Science Foundation of China) 22272122National Natural Science Foundation of China (National Science Foundation of China) 22332004National Natural Science Foundation of China (National Science Foundation of China) 22472122Natural Science Foundation of Hubei Province (Hubei Provincial Natural Science Foundation) 2024AFB571
6 · The paper itself

Abstract

Unveiling the so far ambiguous mechanism of the significant dependence on the identity of alkali metal cation would prompt opportunities to solve the more than two orders of magnitude slowdown of hydrogen electrocatalytic kinetics in base relative to acid, which has hampered the effort to reduce the precious metal usage in fuel cells by using the hydroxide exchange membrane. Herein, we present atomic-scale evidences from ab-initio molecular dynamics simulation and in-situ surface-enhanced infrared absorption spectroscopy which show that it is the apparent discrepancies in the electric double-layer structures induced by differently sized cations that lead to largely different interfacial proton transfer barriers and therefore hydrogen electrocatalytic kinetics in base. Concretely, severe accumulation of larger cation in electric double-layer causes more discontinuous interfacial water distribution and H-bond network, thus rendering the proton transfer from bulk to interface more obstructed. Such notion is strikingly different from the previously envisioned impact of cation-intermediate interactions on the energetics of surface steps, providing a unique interfacial perspective for understanding the ubiquitous cation specificity in electrocatalysis.

Identifiers

PMID39984483
PMCPMC11845716

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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.