过电位
塔菲尔方程
材料科学
尖晶石
电解质
催化作用
过渡金属
化学工程
析氧
无机化学
钴
掺杂剂
分解水
物理化学
兴奋剂
化学
电极
冶金
电化学
光电子学
光催化
工程类
生物化学
作者
Zhangtao Guo,Gaoqi Tian,Lin Liu,Binyu Zhang,Qiang Wu,Chaoyong Yang,Jinchun Tu,Lei Ding,Xiaolin Zhang
标识
DOI:10.1016/j.jmst.2021.02.016
摘要
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.
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