ArticleNature communications2024
Designing neighboring-site activation of single atom via tunnel ions for boosting acidic oxygen evolution.
Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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Who cites it
7 citing papers in PubMed.
- Coordination Engineering of Ir─Mo Atomic Pair Sites to Break Scaling Limitations for Acidic Oxygen Evolution.Angewandte Chemie (International ed. in English) · 2026Article
- Single-Atom Catalysts (SACs) for High-Efficiency Water Electrolysis: A Comprehensive Review.Materials (Basel, Switzerland) · 2026Review
- Oxygen Evolution Reaction Catalysts for Acidic-Media COAdvanced materials (Deerfield Beach, Fla.) · 2026Review
- Synergistic Fe-Ni dual-atom sites on hollow carbon enabling high-performance rechargeable zinc-air batteries.Chemical science · 2026Article
- Cobalt and Yttrium Doping to Activate Dual-Site Mechanism of Amorphous NiFeOOH for Large-Current Water Electrooxidation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Modulating the covalency of Ru-O bonds by dynamic reconstruction for efficient acidic oxygen evolution.Nature communications · 2025Article
- Co-Motif-Engineered RuOACS applied materials & interfaces · 2025Article
Corrections and comments
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Authors and funding
14 authors.
Funding
Abstract
Realizing an efficient turnover frequency in the acidic oxygen evolution reaction by modifying the reaction configuration is crucial in designing high-performance single-atom catalysts. Here, we report a "single atom-double site" concept, which involves an activatable inert manganese atom redox chemistry in a single-atom Ru-Mn dual-site platform with tunnel Ni ions as the trigger. In contrast to conventional single-atom catalysts, the proposed configuration allows direct intramolecular oxygen coupling driven by the Ni ions intercalation effect, bypassing the secondary deprotonation step instead of the kinetically sluggish adsorbate evolution mechanism. The strong bonding of Ni ions activates the inert manganese terminal groups and inhibits the cross-site disproportionation process inherent in the Mn scaffolding, which is crucial to ensure the dual-site platform. As a result, the single-atom Ru-Ni-Mn octahedral molecular sieves catalyst delivers a low overpotential, adequate mass activity and good stability.
Identifiers
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Registered trials
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