Tuning the Surface Electronic Structure of Amorphous NiWO4 by Doping Fe as an Electrocatalyst for OER

• Published in: Inorganic chemistry Vol. 62; no. 30; pp. 11817 - 11828
• Main Authors: N. Dhandapani, Hariharan, Madhu, Ragunath, De, Aditi, Salem, Mohamed A., Ramesh Babu, B., Kundu, Subrata
• Format: Journal Article
• Language: English
• Published: American Chemical Society 31.07.2023
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.3c01095

Water electrolysis is considered as one of the alternative potential approaches for producing renewable energy. Due to the sluggish kinetic nature of oxygen evolution reaction (OER), it encounters a significant overpotential to achieve water electrolysis. Hence, the advancement of cost-effective transition metal-based catalysts toward water splitting has gained global attention in recent years. In this work, the doping of Fe over amorphous NiWO4 increased the OER activity effectively and achieved stable oxygen evolution in the alkaline medium, which show better electrocatalytic activity as compared to crystalline tungstate. As NiWO4 has poor activity toward OER in the alkaline medium, the doping of Fe3+ will tune the electronic structure of Ni in NiWO4 and boost the OER activity. The as-synthesized Fe-doped amorphous NiWO4 exhibits a low overpotential of 230 mV to achieve a current density of 10 mA cm–2 and a lower Tafel slope value of 48 mV dec–1 toward OER in 1.0 M KOH solution. The catalyst also exhibits long-term static stability of 30 h during chronoamperometric study. The doping of Fe improves the electronic conductivity of Ni-3d states in NiWO4 which play a dominant role for better catalytic activity via synergistic interaction between Fe and active Ni sites. In future, these results offer an alternative route for precious metal-free catalysts in alkaline medium and can be explicitly used in various tungstate-based materials to increase the synergism between the doped atom and metal ions in tungstate-based materials for further improvement in the electrocatalytic performance.