Toward High-Performance Hematite Nanotube Photoanodes: Charge-Transfer Engineering at Heterointerfaces

Authors
Kim, Do HongAndoshe, Dinsefa M.Shim, Young-SeokMoon, Cheon-WooSohn, WoonbaeChoi, SeokhoonKim, Taemin LudvicLee, MigyoungPark, HoonkeeHong, KootakKwon, Ki ChangSuh, Jun MinKim, Jin-SangLee, Jong-HeunJang, Ho Won
Issue Date
2016-09
Publisher
American Chemical Society
Citation
ACS Applied Materials & Interfaces, v.8, no.36, pp.23793 - 23800
Abstract
Vertically ordered hematite nanotubes are considered to be promising photoactive materials for high-performance water-splitting photoanodes. However, the synthesis of hematite nanotubes directly on conducting substrates such as fluorine-doped tin oxide (FTO)/glass is difficult to be achieved because of the poor adhesion between hematite nanotubes and FTO/glass. Here, we report the synthesis of hematite nanotubes directly on FTO/glass substrate and high-performance photoelectrochemical properties of the nanotubes with NiFe cocatalysts. The hematite nanotubes are synthesized by a simple electrochemical anodization method. The adhesion of the hematite nanotubes to the FTO/glass substrate is drastically improved by dipping them in nonpolar cyclohexane prior to postannealing. Bare hematite nanotubes show a photocurrent density of 1.3 mA/cm(2) at 1.23 V vs a reversible hydrogen electrode, while hematite nanotubes with electrodeposited NiFe cocatalysts exhibit 2.1 mA/cm(2) at 1.23 V which is the highest photocurrent density reported for hematite nanotubes-based photoanodes for solar water splitting. Our work provides an efficient platform to obtain high-performance water-splitting photoanodes utilizing earth-abundant hematite and noble-metal-free cocatalysts.
Keywords
ALPHA-FE2O3 PHOTOELECTRODES; WATER OXIDATION; NICKEL-IRON; NANORODS; ARRAYS; ELECTRODEPOSITION; PHOTOLYSIS; EFFICIENCY; SUBSTRATE; CATALYSTS; water-splitting photoanode; hematite; nanotube; NiFe cocatalysts; earth abundant
ISSN
1944-8244
URI
https://pubs.kist.re.kr/handle/201004/123694
DOI
10.1021/acsami.6b05366
Appears in Collections:
KIST Article > 2016
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