纳米团簇
过电位
电化学
异质结
X射线光电子能谱
纳米结构
化学工程
催化作用
材料科学
微观结构
纳米技术
化学
物理化学
电极
光电子学
有机化学
工程类
冶金
作者
Kotesh Kumar Mandari,Namgyu Son,Misook Kang
标识
DOI:10.1016/j.ijhydene.2022.11.309
摘要
The development of highly efficient binary heterostructures with enhanced electrocatalytic activities is vital for reducing the energy consumed by the hydrogen evolution reaction (HER). Herein, we successfully design and synthesize an eco-friendly Ag3PO4/1T-2H MoS2 heterostructure to catalyze the HER process. Micromorphology and microstructure studies show that the Ag3PO4 nanoclusters are well dispersed with abundant catalytically active sites on the surface of the 1T-2H MoS2 nanoflowers. X-ray photoelectron spectroscopy confirms the stable oxidation state and electronic interactions in the 2 wt% Ag3PO4/1T-2H MoS2 nanostructure. Benefitting from the strong electronic interactions and advantages of abundant heterogeneous interfaces and catalytically active sites, the 2 wt% Ag3PO4/1T-2H MoS2 heterostructure delivers excellent and durable electrochemical HER activity in alkaline solution, with a low overpotential of 149 mV for the HER at 10 mA cm−2, in clear improvement over 1T-2H MoS2. The enhanced electrocatalytic activity is ascribed to the abundant catalytically active sites, rapid charge transport, and Ag3PO4/1T-2H MoS2 synergism. This study provides a novel strategy for exploring and synthesizing low-cost binary electrocatalysts that enhance the electrochemical HER performance in energy-conversion applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI