J. Mater. Sci. Technol. ›› 2021, Vol. 89: 52-58.DOI: 10.1016/j.jmst.2021.02.016

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Phosphorus substitution into Co3S4 nanoneedle arrays for efficient hydrogen evolution catalysis

Zhangtao Guoa, Gaoqi Tiana, Lin Liua, Binyu Zhanga, Qiang Wub, Yang Caoa,c, Jinchun Tua, Lei Dinga,*(), Xiaolin Zhangc,*()   

  1. aState Key Laboratory of Marine Resource Utilization in South China Sea, School of Materials Science and Engineering, Hainan University, Haikou 570228, China
    bSchool of Tropical Medicine and Laboratory Medicine, MOE Key Laboratory of Emergency and Trauma, Hainan Medical University, Haikou 571199, China
    cKey Laboratory Of Child Cognition & Behavior Development Of Hainan Province, Qiongtai Normal University, Haikou 571127, China
  • Received:2020-11-18 Revised:2021-01-30 Accepted:2021-02-02 Published:2021-10-30 Online:2021-10-30
  • Contact: Lei Ding,Xiaolin Zhang
  • About author:xlzhang0812@gmail.com (X.Zhang).
    *E-mail addresses: Lding@hainanu.edu.cn (L. Ding),

Abstract:

Transition-metal based hybrids with excellent stability and activity are favorable candidates for hydrogen evolution reaction (HER). The development of typical Co3S4 has recently received considerable attention due to the multiple valences of the spinel-structured compound. However, the in-depth effect of the dopants on the HER performance of Co3S4 has not been systematically clarified. Here, we report a sequential synthesis of a spinel-structured cobalt phosphosulfate nanoneedle arrays grown on carbon cloth (namely, P-Co3S4/CC). Results indicate that P-Co3S4/CC exhibits high electrocatalytic performance for HER with a low overpotential of 65 mV to drive10 mA cm-2, a small Tafel slope of 76.6 mV per decade, and great long-term stability for 25 h at various current densities in alkaline electrolyte. The first-principle calculation result reveals that the phosphorous doping work at Co3S4 enhances the HER performance significantly because the tetrahedral Co2+ active sites nearest the P atoms more easily weaken the H-O bond to form intermediates. The experiment result characterization and theoretical calculations further show that the introduction of P atom not only offers more active sites but also improves the electrical conductivity in an alkaline electrolyte solution. Consequently, the identification of active species provides feasible guidance for the further design of high-performance spinel-structured catalysts.

Key words: P-Co3S4/CC, P substitution, Electronic conductivity, HER