塔菲尔方程
静电纺丝
材料科学
化学工程
催化作用
分解水
电催化剂
制氢
电子转移
纳米技术
电极
化学
复合材料
电化学
光化学
光催化
有机化学
聚合物
物理化学
工程类
作者
Jibiao Guan,Wubing Chen,Yini Fang,Lina Wang,Yaqin Fu,Baochun Guo,Ming Zhang
标识
DOI:10.1016/j.ijhydene.2022.03.013
摘要
The substitution of noble metal catalysts with earth abundant TMs as electrocatalysts for hydrogen production is of great significance. One biggest bottleneck for high-efficiency water electrolysis in TM catalysts is the sluggish reaction kinetics or electron transport efficiency. The electrical coupling between the substrate and the catalytic material can accelerate the electron transport, enhancing the charge transfer kinetics, and thereby improve the catalytic performance of the catalyst. Herein, we report a sandwich-structured CNF/Co3S4/MoS2, MoS2 grown in-situ on N-doped nanofibers with Co3S4 nanoparticles via electrospinning, carbonization and hydrothermal process, as self-supported electrodes for hydrogen evolution reaction. The sandwich structure is comprised of CNFs/Co3S4/MoS2 as substrate/accelerator/catalyst. Thereinto, the three-dimensional CNF framework, intrinsically doped by nitrogen, can open accessible channels for reactants and served as substrates for the in-situ growth of Co3S4 and MoS2 nanocrystals with high conductivity and massive active sites. Hence, the CNF/Co3S4/MoS2 shows outstanding catalytical performance in water electrospinning, only 80 mV required to drive 10 mA cm−2 current density with the Tafel slope of 99.2 mV dec−1 in alkaline media. Besides, the performance can be maintained for at least 40 h with negligible decline. This experiment can provide a new idea for the design of efficient and stable self-supporting electrodes.
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