Photoelectrochemical water splitting at nanostructured alpha-Fe2O3 electrodes

Authors
Rahman, GulJoo, Oh-Shim
Issue Date
2012-10
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.37, no.19, pp.13989 - 13997
Abstract
In this study, nanostructured alpha-Fe2O3 thin films were deposited by simple electrodeposition for photoelectrochemical water splitting. Post-annealing temperature was found to have drastic effect on photoactivity of these films. SEM analysis illustrated that size of nanoparticles increases with annealing temperature. The current-potential characteristics showed that the water-splitting photocurrent strongly depends on post-annealing temperature. A maximum photocurrent density of 0.67 mA/cm(2) was observed at 1.23 V versus reversible hydrogen electrode (RHE) under standard illumination conditions (AM 1.5 G 100 mW/cm(2)), and the water-splitting current was over 1.0 mA/cm(2) before the dark current flow starts (at 1.55 V versus RHE). The electrode shows an onset potential as low as 0.8 V (versus RHE) for water photooxidation, which is one of the best results reported for hematite photoanodes. This high photoactivity of electrodes is attributed to the preferential growth of hematite nanostructures along the most conductive plane (001) and incorporation of Sn in film from the substrate at high annealing temperature. The best-performing electrode shows an incident photon conversion efficiency (IPCE) of 12% at 400 nm (in 1 M NaOH at 1.23 V versus RHE), which indicate the improved light-harvesting properties of these nanostructures. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
Keywords
HEMATITE THIN-FILMS; HYDROGEN-PRODUCTION; OXIDE; OXIDATION; DEPOSITION; COMPOSITE; TIO2; HEMATITE THIN-FILMS; HYDROGEN-PRODUCTION; OXIDE; OXIDATION; DEPOSITION; COMPOSITE; TIO2; Hematite thin film; Electrodeposition; Annealing temperature; Onset potential; Water splitting
ISSN
0360-3199
URI
https://pubs.kist.re.kr/handle/201004/128845
DOI
10.1016/j.ijhydene.2012.07.037
Appears in Collections:
KIST Article > 2012
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