Scalable Surface Alloying–Dealloying Manufactures Nanoporous Electrodes From Bulk Metals for Ampere‐Level Alkaline Water Electrolysis
Commercial deployment of alkaline water electrolysis requires electrodes that can sustain ampere-level current densities while remaining manufacturable at scale; however, most advanced electrocatalysts demonstrated in laboratories lack mechanical robustness and are incompatible with industrial production. Here we report a vapor-phase surface alloying-dealloying (VPA-CD) strategy that converts commodity metal sheets directly into bulk-supported nanoporous electrodes via in situ formation of catalyst layers metallurgically bonded to dense substrates. Applied to Ni-Mo and Ni-Fe alloys, this approach yields Mo single-atom-doped nanoporous Ni with high hydrogen evolution activity and nanoporous Ni(Fe)/Ni<sub>3</sub>Fe heterostructures with excellent oxygen evolution activity, enabling ampere-level alkaline electrolysis at low cell voltages. Beyond planar substrates, the method scales to large-area and patterned architectures that directly integrate flow fields and catalyst layers; the resulting integrated electrolyzer achieves 1.0 A cm<sup>-2</sup> at only 1.84 V and remains stable for over 185 h, outperforming commercial benchmarks. These findings establish VPA-CD as a robust and manufacturable route for engineering nanoporous electrodes, bridging the gap between catalyst discovery and device-level hydrogen production.
Authors
- Y Zhang
- Yunfan Han
- Jiuhui Han
- Qi Li (ORCID: https://orcid.org/0000-0002-0033-6204)
- Yi Ding (ORCID: https://orcid.org/0009-0002-6372-5167)
- Cong Xi
- Peng Yue
- Chao Li
- Lin Qiao
- Linji Bi
- Kaiyue Zhang
- Mingwei Chen
Institutions
- Tianjin University of Technology (CN)
- Southern University of Science and Technology (CN)
- University of Edinburgh (GB)
Publication Details
- Journal
- Advanced Materials
- Published
- 2026-02-16
- DOI
- https://doi.org/10.1002/adma.202521570
- Primary Topic
- Nanoporous metals and alloys
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China