Fabrication of Ni <sub>2</sub> Fe-LDHs@WO <sub>3</sub> Composite Photoanodes via Low-Dimensional Engineering toward Enhanced PEC-OER Performance
The development of cost-effective and efficient photoanodes is essential for advancing photoelectrochemical oxygen evolution reaction (PEC-OER) technology. Herein, we report the successful fabrication of Ni2Fe layered double hydroxides (Ni2Fe-LDHs)@WO3 composite photoanodes via a combined approach of ultrasonication-assisted exfoliation and electrostatic self-assembly techniques. The composite was constructed from WO3 nanosheets derived from WO2Cl2 dissociation and Ni2Fe-LDHs nanosheets obtained through exfoliation of bulk Ni2Fe-LDH. Detailed characterization revealed a densely packed, scale-like morphology and strong electronic coupling within the fabricated heterostructured material, facilitating enhanced photon harvesting, optimized charge transport, and accelerated reaction kinetics. Electrochemical tests demonstrated that the composite exhibited a remarkable photocurrent density of 3.62 mA cm–2 at 1.23 V vs RHE, nearly seven times higher than that of pristine WO3. Mechanistic analyses highlighted that the introduction of Ni2Fe-LDHs created a favorable built-in electric field and promoted the formation of high-valence Ni species, significantly enhancing the PEC-OER performance. This study provides a novel strategy for developing advanced solar-driven water splitting materials.
Authors
- Bing Xue (ORCID: https://orcid.org/0000-0003-1535-4023)
- Fangfei Li (ORCID: https://orcid.org/0000-0003-1938-5361)
- Daoxin Liu (ORCID: https://orcid.org/0000-0001-6280-2162)
Institutions
- Ministry of Education of the People's Republic of China (CN)
- Jilin University (CN)
- Ministry of Natural Resources (CN)
- Jilin Medical University (CN)
- Scientific Methods (United States) (US)
Publication Details
- Journal
- The Journal of Physical Chemistry C
- Published
- 2025-12-08
- DOI
- https://doi.org/10.1021/acs.jpcc.5c06277
- Primary Topic
- Advanced Photocatalysis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00