Modulation of Highly Ordered Au–Cu<sub>2</sub>O Core–Satellite Nanostructures for Enhanced Photocatalytic Performance
Janus nanostructures, distinguished by their inherent asymmetry, have attracted considerable attention due to their potential in diverse applications, particularly in photocatalysis. However, conventional single-island Janus structures are limited by their simplified surface architecture, which lead to fewer active sites and restricted electron/photon interaction pathways. Herein, we propose a strategy based on interfacial control to fabricate core-satellite (CSt) nanostructures, wherein polycrystalline Au nanoparticles (pc-Au NPs) serve as seeds for the controlled growth of copper(I) oxide (Cu<sub>2</sub>O) islands. Strong ligand-mediated interfacial interactions enable precise regulation of Cu<sub>2</sub>O growth on polycrystalline Au seeds, leading to well-defined core-satellite configurations. This architecture enhances interfacial area and creates multiple Au-Cu<sub>2</sub>O interfaces that facilitate synergistic charge separation and directional transport. As a result, the core-satellite structures exhibit markedly improved photocatalytic performance compared with their single-island and core-shell counterparts. This work underscores the structural advantages of core-satellite nanostructures and provides a tunable platform for designing high-efficiency photocatalysts in energy conversion and related applications.
Authors
- Yi‐Gang Ji
- Wenjia Xu (ORCID: https://orcid.org/0009-0001-3770-8921)
- Lingyu Zhang (ORCID: https://orcid.org/0000-0002-4297-903X)
- Ruonan Chen (ORCID: https://orcid.org/0000-0003-1758-6151)
- Pan Du (ORCID: https://orcid.org/0000-0002-4229-0902)
- Bao-gen Shen
- Lei Cang
Institutions
- Nanjing Tech University (CN)
- Jiangsu Second Normal University (CN)
- Life University (US)
Publication Details
- Journal
- Inorganic Chemistry
- Published
- 2025-09-16
- DOI
- https://doi.org/10.1021/acs.inorgchem.5c03287
- Primary Topic
- Copper-based nanomaterials and applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00