{
  "abstract": "Transition-metal spinels hold immense promise for the oxygen evolution reaction (OER), yet their inherently strong metal–oxygen bonds severely restrict the activation of lattice oxygen, locking the reaction into the kinetically sluggish adsorbate evolution mechanism (AEM). Herein, we propose a metal–oxygen covalency engineering strategy to modulate the octahedral sites of NiCo2O4 spinel by modifying the tailored Ru and Fe bimetallic ions. The preferential incorporation of high-valent Ru significantly enhances M–O bond covalency and upshifts the O 2p band center, lowering the thermodynamic barrier for the lattice oxygen mechanism (LOM) pathway. Concurrently, the synergistic Fe species functions as an electronic buffer that effectively suppresses metal dissolution and stabilizes the lattice framework, thereby preventing structural collapse. Impressively, the optimal RuFe–NiCo2O4 catalyst bypasses the inherent AEM scaling relationships, delivers an exceptionally low overpotential of 390 mV at 500 mA cm−2 and retains excellent catalytic stability for 800 h in a prototype anion exchange membrane water electrolyzer (AEMWE). This work establishes a highly rational and feasible route for the design of next-generation, industrial-grade water splitting electrocatalysts.",
  "abstract_shown": true,
  "affiliations": [
    "School of Chemistry and Chemical Engineering, Guangzhou University Guangzhou 510006 P. R. China",
    "School of Chemistry, South China Normal University Guangzhou 510006 China"
  ],
  "article_type": "research article",
  "arxiv": null,
  "author_total": 6,
  "authors": [
    {
      "affs": [
        0
      ],
      "name": "Hui-Jian Zhang"
    },
    {
      "affs": [
        0
      ],
      "name": "Zi-Qiang Chen"
    },
    {
      "affs": [
        0
      ],
      "name": "Ren-Hao Ma"
    },
    {
      "affs": [
        0
      ],
      "name": "Zheng-Hao Xuan"
    },
    {
      "affs": [
        0
      ],
      "name": "Xiao-Tong Wang",
      "orcid": "0000-0002-5640-1271"
    },
    {
      "affs": [
        0,
        1
      ],
      "name": "Zhao-Qing Liu",
      "orcid": "0000-0002-0727-7809"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/8fmfw0a10d3zg.bib",
  "cited_by": 0,
  "doi": "10.1039/d6sc05929e",
  "fulltext_url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC13551271/",
  "id": "8fmfw0a10d3zg",
  "issns": [
    "2041-6520",
    "2041-6539"
  ],
  "landing_url": "https://doi.org/10.1039/d6sc05929e",
  "language": "en",
  "licence": "CC-BY-NC-3.0",
  "licence_label": "CC BY-NC 3.0",
  "licence_source": "article",
  "licence_url": "https://creativecommons.org/licenses/by-nc/3.0/",
  "metadata_licence": null,
  "native_subjects": [
    [
      "heading",
      "Chemistry"
    ],
    [
      "openalex",
      "2105|Electrocatalysts for Energy Conversion"
    ]
  ],
  "openalex": "W7204806271",
  "pdf_url": "https://pubs.rsc.org/sc/article-pdf/doi/10.1039/D6SC05929E/13728892/d6sc05929e.pdf",
  "pmcid": "PMC13551271",
  "pmid": "42713032",
  "published": "2026-08-31",
  "publisher": "Royal Society of Chemistry",
  "ris": "https://research.draconitic.com/paper/8fmfw0a10d3zg.ris",
  "sources": [
    {
      "first_seen": "2026-10-31T12:23:45Z",
      "native_id": "PMC13551271",
      "source": "pmc",
      "url": "https://doi.org/10.1039/d6sc05929e"
    }
  ],
  "subjects": [
    {
      "field": "chemistry",
      "origin": "openalex:2105|Electrocatalysts for Energy Conversion",
      "subfield": "electrochemistry-energy"
    }
  ],
  "title": "Metal–oxygen covalency engineering activates stable lattice oxygen in NiCo2O4 spinel for efficient oxygen evolution",
  "title_text": "Metal–oxygen covalency engineering activates stable lattice oxygen in NiCo2O4 spinel for efficient oxygen evolution",
  "type": "peer-reviewed",
  "updated_at": "2026-11-01T12:20:53Z",
  "url": "https://research.draconitic.com/paper/8fmfw0a10d3zg",
  "venue": "Chemical Science",
  "versions": []
}