Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 6, Issue 27, Pages 12978-12984Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta04621b
Keywords
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Funding
- University of Central Florida [20080741]
- Preeminent Postdoctoral Program (P3) at University of Central Florida
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Herein, we explore a strategy for significantly enhancing the photoelectrochemical (PEC) water splitting efficiency by means of a synergistic interaction between plasmonic Au nanoparticles (NPs) and oxygen vacancies in an amorphous black TiO2 (A-B-TiO2) nanoporous film. The interaction between plasmonic metals and semiconductor substrates was investigated, for the first time, showing that A-B-TiO2 would be a better support for plasmonic Au NPs than pristine TiO2 for plasmon-enhanced PEC water splitting. The rationally designed Au@A-B-TiO2 heterostructure significantly increases the plasmonic effect of Au NPs and consequently improves hot electron injection from Au to A-B-TiO2, boosting the separation efficiency of hot electron/hole pairs and leading to considerably improved water splitting performance under solar light irradiation. As a proof-of-concept, the Au@A-B-TiO2 photoelectrode exhibits a photocurrent density of 2.82 mA cm(-2) at 1.23 V vs. RHE under AM 1.5G illumination, which is much higher than those of the state-of-the-art Au-TiO2 photoelectrodes for PEC water splitting.
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