过电位
插层(化学)
电催化剂
塔菲尔方程
剥脱关节
二硫化钼
材料科学
化学工程
层状结构
聚合物
交换电流密度
催化作用
聚丙烯腈
纳米复合材料
氢键
无机化学
石墨烯
纳米技术
化学
电极
电化学
有机化学
物理化学
复合材料
分子
工程类
作者
Xiaohan Lu,Tingxian Tao,Liru Chen,Siyu Lu,Yilin Zhang,Jiaxin Xie,Zhi‐Chuan Wu
标识
DOI:10.1016/j.ijhydene.2022.04.052
摘要
Activity and stability are the kernels of MoS2-based catalysts for hydrogen evolution reactions (HER). Here an intercalation-exfoliation nanocomposite (N–MoS2/AOCF) was designed and successfully synthesized through a facile polymer-solution intercalation method, and the molecular chains of amidoximated polyacrylonitrile (AOCF) with coordinating ability was intercalated into the preintercalated molybdenum disulfide (N–MoS2) nanosheets. The structure characterization demonstrated that N–MoS2 dispersed randomly with a small size and curly lamellar structure. Besides, the interlayer spacing enlarged significantly in the AOCF matrix. Furthermore, N–MoS2 nanosheets are tightly combined with AOCF via the coordination bonds between –OH and –NH2 of AOCF; therefore, the diverse active sites and good stability of N–MoS2/AOCF were attributable to the intense bonding effect, inducing desirable HER performance in acidic medium. Notably, the obtained electrocatalyst exhibited a low overpotential (176 mV at a current density of 10 mA/cm2), a small Tafel slope (51.08 mV/dec), and a large electric double-layer capacitance (39.98 mF/cm2).
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