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Molecular Catalysis· 2026Q2

Carbon‑paper‑supported Fe‑doped WO3 catalysts engineered as a high‑performance bifunctional electrode for alkaline water splitting

Nguyễn Hoàng Phương, Hoa Cong Nguyen, Viet Van Pham

Short summary

Fe-doped WO3 immobilized on carbon paper (Fe:WO3/CP) achieved lower overpotentials for both hydrogen evolution (0.59 V at 10 mA/cm2) and oxygen evolution (0.46 V at 10 mA/cm2) compared to undoped WO3/CP in 1 M KOH, demonstrating enhanced bifunctional activity for alkaline water splitting.

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Key points

  • Fe-doped WO3 immobilized on carbon paper (Fe:WO3/CP) was fabricated using a simple dip-coating method.
  • Fe doping narrowed the optical band gap from 2.57 to 2.42 eV and increased donor density.
  • Fe:WO3/CP electrodes achieved lower overpotentials at 10 mA/cm2: 0.59 V for HER (vs. 0.74 V for WO3/CP) and 0.46 V for OER (vs. 0.71 V for WO3/CP).
  • The Fe:WO3/CP electrode maintained performance for 24 hours of continuous cathodic operation without degradation.

AI-generated from the title and abstract; the full text is not read.

Abstract

Tungsten trioxide (WO 3 ) is an earth‑abundant and chemically robust semiconductor predominantly explored as a photoanode. A key limitation in earlier WO 3 studies is the reliance on fluorine‑doped tin oxide (FTO) substrates, whose flat 2D geometry, moderate conductivity, and susceptibility to reductive degradation restrict catalytic performance. In contrast, carbon paper (CP) offers a 3D porous fiber network with a substantially larger real surface area, superior electrical conductivity, and excellent electrochemical stability in alkaline media, making it a more suitable platform for high‑current water electrolysis. Here, Fe‑doped WO 3 (Fe: WO 3 ) powders were immobilized onto CP using a simple three‑cycle dip‑coating process with a poly(vinyl alcohol)/carbon‑nanotube binder, producing self‑supported Fe: WO 3 /CP electrodes with a geometric area of 1 cm 2 . XRD, FTIR, and Raman analyses show that both WO 3 and Fe:WO 3 crystallize in mixed hexagonal/monoclinic phases, while Fe incorporation broadens and attenuates W–O–W vibrational modes, indicating increased lattice disorder. Cross‑sectional SEM and EDX mapping reveal a continuous 1–2 µm catalyst overlayer with homogeneous W, O, and Fe distribution across the carbon fibers. Fe doping narrows the optical band gap from 2.57 to 2.42 eV, red‑shifts the absorption edge from 481 to 512 nm, and decreases the Mott–Schottky slope, consistent with an increased donor density. Electrochemical testing in 1 M KOH shows that Fe: WO 3 /CP outperforms undoped WO 3 /CP for both half‑reactions: the overpotential at 10 mA cm −2 decreases from 0.74 to 0.59 V for HER and from 0.71 to 0.46 V for OER, while the Tafel slopes decrease from 514.5 to 406.0 mV·dec −1 and from 573.6 to 357.7 mV·dec −1 , respectively. The double‑layer capacitance increases by a factor of 1.65, and the electrode maintains 24 h of continuous cathodic operation without morphological or compositional degradation. These results demonstrate that combining Fe doping with conductive‑carbon immobilization provides a simple and effective route toward WO 3 ‑based bifunctional electrodes with enhanced activity and durability for alkaline water electrolysis.

The authors' abstract, as published at the source. Molecular Catalysis, 2026 · DOI ↗

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Field: Renewable Energy, Sustainability and the Environment

Renewable Energy, Sustainability and the EnvironmentEnergy