Influence of Crystalline Structure and Ti-Doping on Bulk and Surface Properties of ZnFe2O4 Thin Film Photoanodes

Pulsed laser deposition (PLD) was used to grow undoped and Ti-doped ZnFe2O4 compact polycrystalline thin film photoanodes on glass substrates coated with fluorinated tin-oxide (FTO). The film crystallinity was found to have a substantial effect on both the bulk and surface photoelectrochemical (PEC)...

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Bibliographic Details
Published inACS applied energy materials Vol. 7; no. 15; pp. 6105 - 6115
Main Authors Shriqui, Yarden, Rashkovskiy, Alexander, Miriyala, Kumaraswamy, Grave, Daniel A.
Format Journal Article
LanguageEnglish
Published American Chemical Society 12.08.2024
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Summary:Pulsed laser deposition (PLD) was used to grow undoped and Ti-doped ZnFe2O4 compact polycrystalline thin film photoanodes on glass substrates coated with fluorinated tin-oxide (FTO). The film crystallinity was found to have a substantial effect on both the bulk and surface photoelectrochemical (PEC) properties of the films. Films deposited at low substrate temperatures consisted of nanometer sized grains with boundaries present along film the out-of-plane direction resulting in poor charge separation efficiency. Increasing the deposition temperature led to formation of a columnar film structure without grain boundaries in the film out-of-plane direction resulting in an enhancement of both charge separation and charge transfer efficiency. Despite these improvements, bulk losses still dominate the overall PEC performance of ZnFe2O4 and were attributed to limited charge carrier transport lengths as well as nonunity, excitation-wavelength-dependent mobile charge carrier generation. Ti-doping of ZnFe2O4 was investigated and found to be a promising way to improve PEC performance without any significant crystallographic or morphological variations in the thin films. While Ti-doping was shown to have minor effect on bulk charge separation efficiency, a substantial increase in charge transfer efficiency of the ZnFe2O4 photoanodes was observed and attributed to surface state passivation resulting from Ti segregation to the surface.
ISSN:2574-0962
2574-0962
DOI:10.1021/acsaem.4c00122