Evidence map›Paper›PMID 41347616›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Support-Intensified Ir─P/O─Mo Cooperative Linkages for Robust Acidic Water Dissociation.

Jun Mei, Ruipeng Guo, Di Wang, Jing Shang, Jiahao Zhao, Juan Bai, Qianqian Yao, Shixue Dou

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Support-Intensified Ir─P/O─Mo Cooperative Linkages for Robust Acidic Water Dissociation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    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

8 authors.

Jun MeiKey Laboratory for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nanoscience and Materials Engineering, Henan University, Zhengzhou, 450046, China.ORCID https://orcid.org/0000-0002-5766-0603
Ruipeng GuoKey Laboratory for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nanoscience and Materials Engineering, Henan University, Zhengzhou, 450046, China.
Di WangKey Laboratory for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nanoscience and Materials Engineering, Henan University, Zhengzhou, 450046, China.
Jing ShangSchool of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, China.
Jiahao ZhaoKey Laboratory for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nanoscience and Materials Engineering, Henan University, Zhengzhou, 450046, China.
Juan BaiSchool of Chemistry and Physics, Centre for Materials Science, Queensland University of Technology, 2 George Street, Brisbane, Queensland, 4000, Australia.ORCID https://orcid.org/0000-0002-7621-2451
Qianqian YaoKey Laboratory for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nanoscience and Materials Engineering, Henan University, Zhengzhou, 450046, China.
Shixue DouInstitute of Energy Materials Science, University of Shanghai for Science and Technology, 516 Jungong Road, Shanghai, 200093, China.

Funding

Australian Research Council Discovery Early Career Researcher Award DE240101045Joint Fund of Science and Technology R&D Plan of Henan Province 245200810061National Natural Science Foundation of China 52402112Natural Science Foundation of Henan Province 252300421102
6 · The paper itself

Abstract

The efficient production of hydrogen via acidic water electrolysis is hampered by the sluggish kinetics of the oxygen evolution reaction (OER) and the scarcity of robust bifunctional catalysts. Iridium-based materials have been recognized as promising active sites; however, the atomic utilization should be maximized, and the stability requires further enhancement. This work introduces a support-intensified catalyst design that features covalent Ir-P-Mo linkages for achieving robust water dissociation. Theoretical calculations reveal that the Ir─P─Mo bond enhances hydrogen evolution reaction (HER) activity by optimizing hydrogen adsorption, while the Ir─O─Mo bond is more favorable for OER. Guided by this principle, a catalyst with coexisting Ir-O-Mo and Ir-P-Mo linkages is rationally synthesized, which exhibits exceptional bifunctional performance in acid solution, including low overpotentials of 33 mV for HER and 249 mV for OER at 10 mA cm

Indexed as

acidcatalystinterfacemolybdenumphosphorus

Identifiers

PMID41347616
PMCPMC12904053

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.