Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 5, Issue 28, Pages 14697-14706Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ta03878j
Keywords
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Funding
- National Natural Science Foundation of China [61376008, 51102048, U1632121]
- State Key Laboratory of Luminescence and Applications [SKLA-2016-16]
- Innovation Program of Shanghai Municipal Education Commission [14ZZ004]
- Nanotechnology Platform Project of the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan [12024046]
- Core-to-Core Program Advanced Research Networks Type A of the Japan Society for the Promotion of Science (JSPS)
- China Scholarship Council [201506100018]
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Preparation of highly active, stable and earth-abundant photoanodes for water oxidation is an important strategy to meet the demand of developing clean-energy technologies. In this paper, efficient and stable photoanodes based on oxygen-deficient black WO3-x@TiO2-x core-shell nanosheets with precisely controlled shell thickness have been fabricated for photoelectrochemical (PEC) conversion from neutral water solutions. The black WO3-x@TiO2-x core-shell nanosheet photoanode with the shell thickness of similar to 15 nm achieved around 8 times higher photocurrent density (similar to 3.20 mA cm(-2)) than the pure WO3 photoanode at 1.23 V vs. the RHE. An improved onset potential with long-term PEC durability was also realized with the obtained black WO3-x@TiO2-x core-shell nanosheet photoanodes. The promoted PEC water oxidation performance was likely to be originated from enhanced light absorption, interfacial charge transfer and charge separation in these WO3-x@TiO2-x nanosheets which were revealed by finite-difference time-domain simulations and specific band alignment, along with optical and electrochemical spectroscopic evidence. In a word, such black WO3-x@TiO2-x nanosheet photoanodes suggest many exciting opportunities for PEC water splitting toward highly efficient solar fuel generation and many other PEC sensing applications.
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