ArticleNature communications2026
Dynamic ligand-vacancy engineering drives metal dimerization for efficient urea electrooxidation.
Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
The trial behind it
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Who cites it
1 citing paper in PubMed.
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Authors and funding
7 authors.
Funding
Abstract
The electrochemical urea oxidation reaction offers environmental benefits by enabling hydrogen generation and nitrogen recycling. However, catalyst instability caused by surface reconstruction remains a challenge. Here, we develop a heteronuclear vacancy-to-bond strategy that achieves both catalytic activation and structural preservation via atomic-level self-optimization. Using Fe-doped bimetallic frameworks, we construct a self-adaptive coordination microenvironment that dynamically generates controllable ligand vacancies while promoting metal dimerization, leading to shortened interatomic distances. The resulting ligand-vacancy-mediated stabilization delivers an low potential of 1.222 V @ 10 mA cm
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Registered trials
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