Abstract
Efficient photocatalytic CO2 reduction to valuable fuels is an ideal strategy for addressing the energy and environmental crisis. Herein, we developed the Zn-incorporated hollow nanocages, assembled by NiCo-layered double hydroxide ultrathin nanosheets (NiCoZnx-LDH), as highly efficient photocatalysts. Spectroscopic characterization and theoretical calculations demonstrate that Zn doping leads to an upshift of the d-band center of Ni-Co dual sites, increasing unoccupied antibonding orbitals and enhancing the binding strength of adsorbates. Therefore, NiCoZn0.10-LDH with the upgrade of d-band shows a lower ·CO2– formation energy, resulting in a more effective stabilization of the rate-limiting ·CO2– intermediate. This boosts the overall CO2 photoreduction performance over NiCoZn0.10-LDH, resulting in a high CO yield of 158.1 μmol·g–1·h–1 with 92.1% selectivity. Our findings enrich the fundamental understanding of the CO2 activation mechanism and provide additional insights into the d-band center theory to enhance the photocatalytic activity for overall CO2 reduction.
| Original language | English |
|---|---|
| Article number | e9120191 |
| Number of pages | 11 |
| Journal | Nano Research Energy |
| Volume | 4 |
| Issue number | 4 |
| Early online date | 14 Oct 2025 |
| DOIs | |
| Publication status | Published - 1 Dec 2025 |
Keywords
- Overall CO2 photoreduction
- Zn doping
- Oxygen vacancy
- d-band center
- CO2 activation
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