过电位
催化作用
化学
X射线光电子能谱
吸附
磷化物
磷酸盐
Zeta电位
金属
化学工程
镍
物理
过渡金属
无机化学
材料科学
电化学
纳米技术
物理化学
有机化学
电极
纳米颗粒
物理层
计算机科学
电信
无线
工程类
作者
Yinling Wang,Nannan Ma,Mingli Fan,Wujian Tang
标识
DOI:10.1149/1945-7111/ac3594
摘要
Transition metal phosphides (TMP) are excellent non-precious metal electrocatalysts for hydrogen evolution reaction (HER). The generation of PO 4 3− before and during the HER process may be inevitable due to the instability of TMP. To investigate the effect of PO 4 3− on the HER catalytic activity of electrocatalysts in alkaline medium, NiCo-S nanotubes were modified with phytate (PHY) with six phosphate groups via adsorption. The successful modification was verified by zeta potential, FT-IR, element mapping, XPS, etc The NiCo-S/PHY displayed a higher HER activity than original NiCo-S. Under the optimum adsorption time (7 h), the overpotential at 10 mA cm −2 ( η 10 ) of NiCo-S/PHY (173 mV) was only half that of the original NiCo-S (346 mV). The role of PO 4 3− was discussed in detail. Moreover, this strategy was extended to NiCo-S grown directly on nickel foam (NiCo-S/NF) and the corresponding NiCo-S/PHY/NF also showed superior HER activity and good stability. This work provides a new strategy to improve the HER activity of electrocatalysts and also a novel perspective for the HER mechanism of TMP.
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