Chinese Journal of Catalysis ›› 2024, Vol. 61: 269-280.DOI: 10.1016/S1872-2067(24)60037-9

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In situ surface reconstruction of heterostructure Ni2P/CoP/FeP4 nanowires network catalyst for high-current-density overall water splitting

Ting Zhaoa, Bingbing Gongb,*(), Guancheng Xua, Jiahui Jianga, Li Zhanga,b,*()   

  1. aState Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, College of Chemistry, Xinjiang University, Urumqi 830017, Xinjiang, China
    bCollege of Chemical Engineering, Xinjiang University, Urumqi 830017, Xinjiang, China
  • Received:2024-01-27 Accepted:2024-04-07 Online:2024-06-18 Published:2024-06-20
  • Contact: * E-mail: gongbb@xju.edu.cn (B. Gong), zhangli420@xju.edu.cn (L. Zhang).
  • Supported by:
    National Natural Science Foundation of China(22369016);National Natural Science Foundation of China(22065034);Natural Science Foundation of Xinjiang Uygur Autonomous Region(2022D01E36);Natural Science Foundation of Xinjiang Uygur Autonomous Region(2022D01E38)

Abstract:

Considering the imperative need for cost-effective electrocatalysts for water electrolysis, a novel Ni2P/CoP/FeP4/IF electrocatalyst nanowires network was synthesized in this study. Owing to the strong synergistic effects and high exposure of the active sites, Ni2P/CoP/FeP4/IF exhibited exceptional performance in both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), demonstrating low overpotentials of 218 and 127 mV at 100 mA cm-2 in alkaline media, respectively. Furthermore, the water electrolyzer based on Ni2P/CoP/FeP4/IF bifunctional catalyst requires only 1.50 and 2.05 V to reach 10 and 500 mA cm-2, respectively, indicating its potential for large-scale hydrogen production. Comprehensive ex situ characterizations and in situ Raman spectra reveal that Ni2P/CoP/FeP4/IF undergoes rapid reconstruction during the OER to form the corresponding (oxy) hydroxide species, which serve as the real active sites. Furthermore, density functional theory calculations clarified that during the HER process, H2O is adsorbed at the Fe site of Ni2P/CoP/FeP4/IF for hydrolysis, with the resultant H* adsorbed at the Ni site for desorption. Introducing CoP promoted water adsorption and increased the HER activity of the catalyst. Hence, this study offers a pathway for designing highly efficient catalysts that leverage the interface effects.

Key words: Overall water splitting, Multi-interfaces, Phosphide, Surface reconstruction, High-current-density