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Activating a Semiconductor-Liquid Junction via Laser-Derived Dual Interfacial Layers for Boosted Photoelectrochemical
Jie Jian1,2, Shiyuan Wang1,2, Qian Ye1,2
1State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Analytical and Testing Center, Northwestern Polytechnical University and Shaanxi Joint Laboratory of Graphene (NPU), Xi'an, 710072, P. R. China.
Researchers developed dual interfacial layers using laser-generated carbon dots to enhance both activity and stability in bismuth vanadate (BiVO4) photoanodes for photoelectrochemical (PEC) hydrogen generation.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- The semiconductor-liquid junction (SCLJ) is crucial for photoelectrochemical (PEC) catalysis, impacting photoelectrode performance in hydrogen generation.
- Achieving both high activity and stability simultaneously at the SCLJ remains a significant challenge in PEC research.
Purpose of the Study:
- To engineer a novel dual interfacial layer configuration for BiVO4 photoanodes.
- To synchronously enhance photoelectrochemical activity and operational stability of BiVO4 photoanodes.
Main Methods:
- Grafting laser-generated carbon dots with phenolic hydroxyl groups (LGCDs-PHGs) to form dual interfacial layers.
- Fabrication of FeNiOOH-LGCDs-PHGs-MBVO photoanodes.
- Characterization of photocurrent density and operational stability.
Main Results:
- The dual interfacial layers effectively inhibited photocorrosion through uniform LGCDs with covalent anchoring.
- Enhanced charge separation and transfer kinetics were observed within each layer.
- Achieved a photocurrent density of 6.08 mA cm⁻² at 1.23 VRHE and operational stability up to 120 hours.
Conclusions:
- The unique dual interfacial layer configuration boosts both photoelectrochemical activity and stability of BiVO4 photoanodes.
- The strategy using LGCDs-PHGs offers a universal approach for improving semiconductor photoelectrode performance.
- Further exploration with catecholic molecules could broaden the applicability of this interfacial engineering strategy.
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