Direct Seawater Hydrogen Evolution via Atomically Precise Regulation of Interfacial pH and Ion‐Water Interactions
at an overpotential of 292 mV and retains exceptional stability (> 500 h) under intermittent renewable-energy operation, with one-tenth the Pt loading of commercial Pt/C. This work establishes a pH gradient-mediated interfacial chemistry framework enabled by atomically precise engineering, providing guidance for sustainable and efficient direct seawater hydrogen evolution.
Authors
- Qisheng Yan (ORCID: https://orcid.org/0009-0008-1398-6135)
- Zhipu Zhang (ORCID: https://orcid.org/0000-0003-2148-8378)
- W HU
- Qiaofeng Yao (ORCID: https://orcid.org/0000-0002-5129-9343)
- Xinxin Pan
- Moshuqi Zhu
- Qiang Zhao (ORCID: https://orcid.org/0000-0002-1636-9254)
- Shanshan Lu (ORCID: https://orcid.org/0000-0001-8931-0416)
- Qing Tang (ORCID: https://orcid.org/0000-0003-0805-7506)
- Qi Chen
Institutions
- Chongqing University (CN)
- Tianjin University (CN)
- Civil Aviation University of China (CN)
- Collaborative Innovation Center of Chemical Science and Engineering Tianjin (CN)
- Fuzhou University (CN)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2026-05-11
- DOI
- https://doi.org/10.1002/anie.7140350
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China