Abstract
Dual-site lattice doping in semiconductor materials is highly promising for photocatalysis as it can tune the sub-band electronic structure and charge distribution of the photocatalyst. However, it is challenging to precisely regulate the band structure by dual-site doping using the same heteroatom. Herein, we report the homogeneous dual-site P lattice doping in CdS quantum rods, i.e. P is homogeneously doped into both substitutional site of S and interstitial site, leading to negative shift of valence and conduction bands with extraordinary visible-light excitation efficiency. The electrons generated in the newly designed photocatalyst have strong redox potential in reducing H+ into H2 in photocatalysis. By introducing nontrivial co-catalyst Ni3C quantum dots onto the surface of P-CdS quantum rods, the apparent quantum efficiency of the catalyst achieves 15.7% at 435 nm, which is 5 times higher than that of pristine CdS.
| Original language | English |
|---|---|
| Article number | 116594 |
| Journal | Chemical Engineering Science |
| Volume | 238 |
| DOIs | |
| State | Published - 20 Jul 2021 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- CdS quantum rod
- Homogeneous dual-site P doping
- Hydrogen evolution
- NiC QDs
- Photocatalysis
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