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Updated: Feb 15, 2026

Photodeposition of Pd onto Colloidal Au Nanorods by Surface Plasmon Excitation
Published on: August 15, 2019
Boosting electrocatalytic hydrogen evolution by plasmon-driven hot-electron excitation.
Hai-Xia Zhang1, Yang Li, Min-Yu Li
1State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, P. R. China. zhang.huabin@ntu.edu.sg zhj@fjirsm.ac.cn.
Localized surface plasmon resonance on gold nanoparticles significantly boosts hydrogen evolution reaction (HER) for water splitting. Porous N-doped carbon enhances charge transfer, improving renewable energy conversion efficiency.
Area of Science:
- Materials Science
- Catalysis
- Renewable Energy
Background:
- Electrocatalytic and photoelectrochemical water splitting are key for renewable energy storage.
- Developing high-performance catalysts is crucial for efficient water splitting.
- Gold nanoparticles (Au NPs) show potential as catalysts.
Purpose of the Study:
- To investigate the effect of localized surface plasmon resonance (LSPR) on Au nanoparticles for hydrogen evolution reaction (HER).
- To enhance HER efficiency using porous N-doped carbon supported Au nanoparticles.
- To explore light-assisted catalytic water splitting systems.
Main Methods:
- Synthesis of porous N-doped carbon supported Au nanoparticles.
- Electrocatalytic testing for HER under illumination.
- Characterization of catalyst properties and charge transfer mechanisms.
Main Results:
- Photon-induced LSPR excitation on Au nanoparticles dramatically improved HER.
- Achieved a >4-fold increase in current density.
- Reduced overpotential to 99 mV at 10 mA cm⁻².
- N-doped carbon facilitated efficient charge transfer from plasmonic Au NPs.
Conclusions:
- Plasmonic excitation significantly enhances HER catalysis efficiency.
- N-doped carbon supports improve charge injection from Au NPs.
- This approach offers new strategies for designing light-assisted water splitting systems.
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