Ultrathin hematite films deposited layer-by-layer on a TiO2 underlayer for efficient water splitting under visible light
Ultrathin hematite (α-Fe2O3) film deposited on a TiO2 underlayer as a photoanode for photoelectrochemical water splitting was described. The TiO2 underlayer was coated on conductive fluorine-doped tin oxide (FTO) glass by spin coating. The hematite films were formed layer-by-layer by repeating the s...
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Veröffentlicht in: | International journal of hydrogen energy 2014-09, Vol.39 (27), p.14604-14612 |
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Sprache: | eng |
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Zusammenfassung: | Ultrathin hematite (α-Fe2O3) film deposited on a TiO2 underlayer as a photoanode for photoelectrochemical water splitting was described. The TiO2 underlayer was coated on conductive fluorine-doped tin oxide (FTO) glass by spin coating. The hematite films were formed layer-by-layer by repeating the separated two-phase hydrolysis-solvothermal reaction of iron(III) acetylacetonate and aqueous ammonia. A photocurrent density of 0.683 mA cm−2 at +1.5 V vs. RHE (reversible hydrogen electrode) was obtained under visible light (>420 nm, 100 mW cm−2) illumination. The TiO2 underlayer plays an important role in the formation of hematite film, acting as an intermediary to alleviate the dead layer effect and as a support of large surface areas to coat greater amounts of Fe2O3. The as-prepared photoanodes are notably stable and highly efficient for photoelectrochemical water splitting under visible light. This study provides a facile synthesis process for the controlled production of highly active ultrathin hematite film and a simple route for photocurrent enhancement using several photoanodes in tandem.
•Ultrathin hematite films on TiO2/FTO were synthesized in control thickness by two-phase hydrolysis.•TiO2 underlayer alleviated dead layer and enhanced hematite light harvesting.•Photoelectrochemical performance was dramatically enhanced by TiO2 underlayer.•A photocurrent of 0.683 mA cm−2 and IPCE of 19.8% were obtained at +1.5 V vs. RHE. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2014.07.120 |