First Evidence and Role of γ -Fe2O3 Seeds in Low-Temperature-Processed Sn-Doped Hematite Photoanodes

Sn doping is an effective strategy to improve the photoelectrochemical response of hematite photoanodes, but its activation typically requires high-temperature treatments that can degrade conductive substrates and limit device integration. Considering photoelectrochemical water splitting as a case study, this work investigates the mechanism of photoelectrochemical activation of Sn-doped hematite-based photoanodes by oxidative annealing of thin metallic Fe-Sn alloy films at a low temperature. X-ray absorption spectroscopy, Raman spectroscopy, grazing-incidence X-ray diffraction, and electron paramagnetic resonance reveal that while hematite is the main crystalline phase, poorly ordered γ-Fe2O3 seeds selectively form in Sn-containing films annealed at 450 °C and progressively transform into Sn-doped α-Fe2O3 at higher annealing temperatures. Under solar illumination in 1 M KOH, photoanodes annealed at 450 °C exhibit photocurrent density (≈480 μA/cm2) and onset potential (≈0.9 V vs RHE) comparable to those obtained after annealing at a higher temperature (750 °C). Sn K-edge X-ray absorption spectroscopy identifies Sn4+ in local Sn-Fe coordination environments consistent with incorporation into the hematite lattice. The γ-Fe2O3 domains may act as transient Sn reservoirs, accommodating Sn beyond the hematite solubility limit and promoting the formation of well-ordered, photoactive Sn-doped α-Fe2O3 nanocrystals, while limiting SnO2 segregation at an Sn/(Fe + Sn) atomic ratio of approximately 3 at %. Control films deposited under an oxygen atmosphere contain a lower γ-Fe2O3 fraction and show poor activity, indicating that low-temperature activation arises not from Sn addition alone but requires oxidation-driven restructuring of the metallic Fe-Sn precursor. The γ-Fe2O3 seeds represent structural fingerprints of a synthesis pathway that enables efficient Sn incorporation and low-thermal-budget fabrication of hematite photoanodes for solar water splitting.

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Journal
ACS Applied Materials & Interfaces
Published
2026-10-28
DOI
https://doi.org/10.1021/acsami.6c15012
Primary Topic
Iron oxide chemistry and applications
Type
article
Field-Weighted Citation Impact
0.00

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article

First Evidence and Role of γ -Fe2O3 Seeds in Low-Temperature-Processed Sn-Doped Hematite Photoanodes

Boris Kalinic, Chiara Maurizio, P. Ragonese, Lorenzo Franco et al.
ACS Applied Materials & Interfaces
Iron oxide chemistry and applications
article

First Evidence and Role of γ -Fe2O3 Seeds in Low-Temperature-Processed Sn-Doped Hematite Photoanodes

Boris Kalinic, Chiara Maurizio, P. Ragonese, Lorenzo Franco, G. Mattei, G. Mattioli, N. W. Naveenkumar
article en

Abstract

Sn doping is an effective strategy to improve the photoelectrochemical response of hematite photoanodes, but its activation typically requires high-temperature treatments that can degrade conductive substrates and limit device integration. Considering photoelectrochemical water splitting as a case study, this work investigates the mechanism of photoelectrochemical activation of Sn-doped hematite-based photoanodes by oxidative annealing of thin metallic Fe-Sn alloy films at a low temperature. X-ray absorption spectroscopy, Raman spectroscopy, grazing-incidence X-ray diffraction, and electron paramagnetic resonance reveal that while hematite is the main crystalline phase, poorly ordered γ-Fe2O3 seeds selectively form in Sn-containing films annealed at 450 °C and progressively transform into Sn-doped α-Fe2O3 at higher annealing temperatures. Under solar illumination in 1 M KOH, photoanodes annealed at 450 °C exhibit photocurrent density (≈480 μA/cm2) and onset potential (≈0.9 V vs RHE) comparable to those obtained after annealing at a higher temperature (750 °C). Sn K-edge X-ray absorption spectroscopy identifies Sn4+ in local Sn-Fe coordination environments consistent with incorporation into the hematite lattice. The γ-Fe2O3 domains may act as transient Sn reservoirs, accommodating Sn beyond the hematite solubility limit and promoting the formation of well-ordered, photoactive Sn-doped α-Fe2O3 nanocrystals, while limiting SnO2 segregation at an Sn/(Fe + Sn) atomic ratio of approximately 3 at %. Control films deposited under an oxygen atmosphere contain a lower γ-Fe2O3 fraction and show poor activity, indicating that low-temperature activation arises not from Sn addition alone but requires oxidation-driven restructuring of the metallic Fe-Sn precursor. The γ-Fe2O3 seeds represent structural fingerprints of a synthesis pathway that enables efficient Sn incorporation and low-thermal-budget fabrication of hematite photoanodes for solar water splitting.

ACS Applied Materials & Interfaces
University of Padua (IT)
European Synchrotron Radiation Facility, Ministero dell'Università e della Ricerca
Affordable and clean energy
Openalex Percentile: Top 35%
Iron oxide chemistry and applications
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