{"title":"Sol–Gel Synthesized Co-Doped Ilmenite-NiTiO3 for Oxygen Evolution Reaction: Interplay of Inductive Effect and Crystal Structure","authors":"Shraddha Jaiswal, Subash Chandra Gupta, Asha Gupta","doi":"10.1002/cctc.202500396","DOIUrl":null,"url":null,"abstract":"<p>The oxygen evolution reaction is key to advancing hydrogen production, energy storage, and sustainable energy technologies. In this study, we have explored the ilmenite-type Co-substituted NiTiO<sub>3</sub> as a promising OER catalyst in the alkaline electrolyte. Synergistic interaction between Ni and Co generates the inductive effect which enhances the ionicity of Ni─O bond leading to a greater overlap between Ni(3<i>d</i>) and O(2<i>p</i>) orbitals, resulting in a higher OER activity of the doped catalysts. Further presence of surface active Co<sup>3+</sup> in the ilmenite structure plays a key role in the enhancement of OER activity of the catalyst. A systematic investigation of the OER activity of Ni<sub>1-x</sub>Co<sub>x</sub>TiO<sub>3</sub> (0 < x < 0.25) with different amounts of Co doping synthesized via sol–gel method is reported here. Among the compositions investigated, Ni<sub>0.825</sub>Co<sub>0</sub>.<sub>175</sub>TiO<sub>3</sub> is the most active as it exhibits excellent activity with a Tafel slope of 56 mV dec<sup>−1</sup> and a overpotential of 395 mV at 10 mA cm<sup>−2</sup>. This work presents the role of the inductive effect originating due to the difference in the electronegativity of neighboring cations, leading to alteration of the redox energies and facilitating the effective electron transfer required for the electrocatalytic OER, which can be further utilized to develop superior electrocatalysts.</p>","PeriodicalId":141,"journal":{"name":"ChemCatChem","volume":"17 12","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemCatChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cctc.202500396","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The oxygen evolution reaction is key to advancing hydrogen production, energy storage, and sustainable energy technologies. In this study, we have explored the ilmenite-type Co-substituted NiTiO3 as a promising OER catalyst in the alkaline electrolyte. Synergistic interaction between Ni and Co generates the inductive effect which enhances the ionicity of Ni─O bond leading to a greater overlap between Ni(3d) and O(2p) orbitals, resulting in a higher OER activity of the doped catalysts. Further presence of surface active Co3+ in the ilmenite structure plays a key role in the enhancement of OER activity of the catalyst. A systematic investigation of the OER activity of Ni1-xCoxTiO3 (0 < x < 0.25) with different amounts of Co doping synthesized via sol–gel method is reported here. Among the compositions investigated, Ni0.825Co0.175TiO3 is the most active as it exhibits excellent activity with a Tafel slope of 56 mV dec−1 and a overpotential of 395 mV at 10 mA cm−2. This work presents the role of the inductive effect originating due to the difference in the electronegativity of neighboring cations, leading to alteration of the redox energies and facilitating the effective electron transfer required for the electrocatalytic OER, which can be further utilized to develop superior electrocatalysts.
期刊介绍:
With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.