Wang Zhichong, Wang Kaixuan, Pan Yajuan, Ye Qing, Zhang Chenxi, Zhang Dan, Zhao Yanxia, Cheng Yongliang
Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, China.
Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, China.
J Colloid Interface Sci. 2025 Jan 15;678(Pt C):886-896. doi: 10.1016/j.jcis.2024.09.166. Epub 2024 Sep 19.
The incorporation of oxyanion groups offers a greater potential for enhancing the activity of oxygen evolution reaction (OER) electrocatalysts compared to traditional metal cations doping, owing to their unique configurations and high electronegativity. However, the incorporation of oxyanion groups that differ from those derived from the oxidation of anions in transition metal monoxides poses significant challenges, thereby limiting further applications of oxyanion group modification approach. Herein, we present a novel sulfate salt assistant approach to fabricate Fe-doped NiP modified with SO/carbon (Fe-NiP-S/C) nanofibers as highly efficient OER electrocatalyst. The optimized Fe-NiP-S/C nanofibers display superb OER activity, requiring low overpotentials of 266, 323, and 357 mV at 100, 500, and 1000 mA cm, respectively. Theoretical calculations reveal that the co-adsorption of PO and SO on the surface of reconstructed electrocatalyst can reduce the energy barrier of rate-determining step, thereby resulting in enhanced OER activity. The present study emphasizes the crucial role played by anion groups in OER activity as well as proposes a novel approach for incorporating anion groups into electrocatalysts.
