Journal of Materials Chemistry · 2012 · 74 citations · 30 references
Natural SciencesMaterials EngineeringMaterials ScienceCrystal StructureElectrochemistryMaterials ChemistryElectrode MaterialsMetal Oxide NanomaterialsPhotochemistryPhotoelectrochemical MaterialsPhotoelectrochemistryRedox-active MaterialsDopant DiffusionDoped Electrode MaterialsHematiteMagnetic PropertiesNanostructured PhotoelectrodesPhotocurrent GenerationPhotoelectrochemical Water SplittingTin Oxides
We present a new, easily scalable method for the deposition of nanocrystalline hematite photoelectrodes based on the spin-coating of a mixed solution containing tin(II) and iron(III) chlorides followed by thermal treatment. Our facile approach does not require any additional film-forming organic species and allows simple control of the photoelectrochemical performance of the electrode by adjusting the degree of tin doping. When annealed at 650 °C a strong increase in the water oxidation photocurrent is observed with increasing tin concentration. The maximum performance (0.45 mA cm−2 at 1.43 V vs. RHE) was found at the highest possible tin loading (20 : 100, Sn : Fe). The contrasting performance of electrodes annealed at 650 °C and 800 °C suggests different activation processes for dopant diffusion and activation. The doping of tin into the crystal structure of hematite thin films is directly evidenced by X-ray photoelectron spectroscopy and indirectly by changes in the intrinsic magnetic parameters (Morin temperature, Néel temperature) of the hematite films. The magnetization measurements thus represent a potential technique to quantify doping amounts in hematite.
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Sn-Doped Hematite Nanostructures for Photoelectrochemical Water Splitting
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