Journal
NANO LETTERS
Volume 17, Issue 4, Pages 2490-2495Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.7b00184
Keywords
Hematite; photoanode; morphology engineering; dopant engineering; water oxidation
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Funding
- Natural Science Foundation of China [21476271]
- NSFC-RGC [21461162003]
- Science and Technology Planning Project of Guangdong Province, China [2014A030308012, 2014KTSCX004]
- China Scholarship Council
- Chancellor's Dissertation-year Fellowship by University of California, Santa Cruz
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High-temperature activation has been commonly used to boost the photoelectrochemical (PEC) performance of hematite nanowires for water oxidation, by inducing Sn diffusion from fluorine-doped tin oxide (FTO) substrate into hematite. Yet, hematite nanowires thermally annealed at high temperature suffer from two major drawbacks that negatively affect their performance. First, the structural deformation reduces light absorption capability of nanowire. Second, this passive doping method leads to nonuniform distribution of Sn dopant in nanowire and limits the Sn doping concentration. Both factors impair the electrochemical properties of hematite nanowire. Here we demonstrate a silica encapsulation method that is able to simultaneously retain the hematite nanowire morphology even after high-temperature calcination at 800 degrees C and improve the concentration and uniformity of dopant distribution along the nanowire growth axis. The capability of retaining nanowire morphology allows tuning the nanowire length for optimal light absorption. Uniform distribution of Sn doping enhances the donor density and charge transport of hematite nanowire. The morphology and doping engineered hematite nanowire photoanode decorated with a cobalt oxide-based oxygen evolution reaction (OER) catalyst achieves an outstanding photocurrent density of 2.2 mA cm(-2) at 0.23 V vs Ag/AgCl. This work provides important insights on how the morphology and doping uniformity of hematite photoanodes affect their PEC performance.
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