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dc.contributor.authorTahir, AA
dc.contributor.authorMat-Teridi, MA
dc.contributor.authorWijayantha, KGU
dc.date.accessioned2016-03-16T10:17:51Z
dc.date.accessioned2016-03-16T13:19:34Z
dc.date.issued2014-01-01
dc.description.abstractNanostructured α-Fe2O3 thin film electrodes were deposited by aerosol-assisted chemical vapour deposition (AACVD) for photoelectrochemical (PEC) water splitting on conducting glass substrates using 0.1 M methanolic solution of Fe(acac)3. The XRD analysis confirmed that the films are highly crystalline α-Fe2O3 and free from other iron oxide phases. The highly reproducible electrodes have an optical bandgap of ~2.15 eV and exhibit anodic photocurrent. The current-voltage characterization of the electrodes reveals that the photocurrent density strongly depended on the film morphology and deposition temperature. Scanning electron microscopy (SEM) analysis showed a change in the surface morphology with the change in deposition temperature. The films deposited at 450 °C have nanoporous structures which provide a maximum electrode/electrolyte interface. The maximum photocurrent density of 455 μA/cm2 was achieved at 0.25 V vs. Ag/AgCl/3M KCl (~1.23 V vs. RHE) and the incident photon to electron conversion efficiency (IPCE) was 23.6% at 350 nm for the electrode deposited at 450 °C.en_GB
dc.identifier.citationVol. 8, pp. 976 - 981en_GB
dc.identifier.doi10.1002/pssr.201409049
dc.identifier.urihttp://hdl.handle.net/10871/20739
dc.language.isoenen_GB
dc.publisherWiley-VCH Verlagen_GB
dc.rightsThis work was supported by the EPSRC award EP/F057342/1 and MOHE award FRGS/2/2013/TK06/UKM/03/1.en_GB
dc.subjectFe2O3en_GB
dc.subjectaerosol assisted chemical vapour depositionen_GB
dc.subjectphotoelectrochemical water splittingen_GB
dc.subjectthin filmsen_GB
dc.titlePhotoelectrochemical properties of texture-controlled nanostructured α-Fe2O3 thin films prepared by AACVDen_GB
dc.typeArticleen_GB
dc.date.available2016-03-16T10:17:51Z
dc.date.available2016-03-16T13:19:34Z
dc.identifier.issn1862-6254
dc.descriptionThis is the author accepted manuscript. The final version is available from the publisher via the DOI in this record.en_GB
dc.identifier.journalPhysica Status Solidi - Rapid Research Lettersen_GB


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