Abstract
Maximizing the utilization of photogenerated electrons and holes to drive the coupling reaction of hydrogen evolution with selective value-added organic synthesis holds great potential for more efficient exploitation of solar energy. Herein, the interstitial boron-doped CdS is synthesized by taking SiO2 as a template as well as the adsorption sites of boric acid, which contributes to the boron doping and induces the reinforced Cd─Se bonding for enhancing the interfacial interaction with co-catalyst MoSe2. Thus, the interfacial Cd─Se bond with more electron localization provides rapid channels at the atomic level for accelerating the charge transfer with a lower energy barrier, achieving the efficient hydrogen evolution and high selectivity pyruvic acid synthesis concurrently. This work provides a new perspective in avoiding the use of sacrificial agents uneconomically and producing green hydrogen with high-value-added chemicals simultaneously.
| Original language | English |
|---|---|
| Article number | 2401285 |
| Journal | Advanced Energy Materials |
| Volume | 14 |
| Issue number | 32 |
| DOIs | |
| State | Published - 23 Aug 2024 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- interfacial chemical bond
- interstitial boron doping
- photocatalytic hydrogen evolution
- pyruvic acid synthesis
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