电催化剂
过电位
析氧
异质结
催化作用
阳极
分解水
材料科学
化学工程
电解
无机化学
联氨(抗抑郁剂)
电化学
化学
电极
物理化学
光电子学
有机化学
光催化
工程类
电解质
色谱法
作者
Ayan Mondal,Harish Reddy Inta,Avishek Roy,Ashok Kumar Mahato,Venkataramanan Mahalingam
标识
DOI:10.1021/acsanm.3c01825
摘要
The design and development of efficient and low-cost electrocatalysts for both anodic (oxygen evolution reaction (OER)/hydrazine oxidation reaction (HzOR)) and cathodic (hydrogen evolution reaction (HER)) reactions are the major challenges for cleaner hydrogen production. Especially, the fabrication of electrocatalysts with abundant electrochemically active sites through simple synthetic routes is of great interest to draw excellent catalytic efficiency. This report provides a strategy to prepare CoS2–MoS2 heterostructures and spheroid-like CoS2 through the sulfurization reaction from the common Co3O4 nanocube precursor in the presence and absence of the molybdenum precursor, respectively. The as-prepared CoS2–MoS2 (25) heterostructure (prepared with 25 mg of Co3O4) shows excellent HER activity in 1 M KOH by delivering a current density of 10 mA/cmgeo2 at an overpotential of 92.5 ± 3.1 mV. The observed enhancement in the HER activity is attributed to the improved water dissociation kinetics at the abundant interfacial area shared between the two components of the heterostructure. Besides, spheroid-like CoS2 shows good OER and hydrazine oxidation reaction (HzOR) activity owing to the high electrochemically active surface area. In addition, the alkaline electrolyzer (HER//OER) constructed using the CoS2–MoS2 (25) heterostructure and spheroid-like CoS2 as the cathode and anode, respectively, delivers a current density of 10 mA/cmgeo2 at a cell potential of 1.67 V. Furthermore, the hydrazine-assisted electrolyzer (HER//HzOR) displays a low cell potential of 0.53 V to attain the same current density along with excellent durability up to 30 h.
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