Active-Site-Rich 1T-Phase CoMoSe2Integrated Graphene Oxide Nanocomposite as an Efficient Electrocatalyst for Electrochemical Sensor and Energy Storage Applications

石墨烯 电催化剂 电化学 超级电容器 氧化物 纳米复合材料 化学 化学工程 拉曼光谱 材料科学 X射线光电子能谱 电极 纳米技术 有机化学 物理化学 工程类 物理 光学
作者
Ramaraj Sukanya,Mani Sakthivel,Shen‐Ming Chen,Kuo–Chuan Ho
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:91 (13): 8358-8365 被引量:43
标识
DOI:10.1021/acs.analchem.9b01152
摘要

The presence of defect/distortion on layered structure of metal chalcogenides facilitate the higher electronic conductivity and electrocatalytic activity. In this work, we have successfully synthesized Co-doped MoSe2(CoMoSe2, Co2MoSe2, Co3MoSe2, and Co4MoSe2) in 1T phase crystal structure by using hydrothermal technique and integrated with graphene oxide (GO). Various analytical techniques such as TEM, STEM, FESEM, XRD, RAMAN, EDX, ICP, and XPS confirmed the formation of 1T phase and defective sites on Co-doped MoSe2. Consequently, the relevant electrochemical studies were followed and reported the significant enhancement in electrocatalytic activity of MoSe2 due to the Co doping and GO hybridization. The proposed GO@CoMoSe2 electrocatalyst was developed to an electrode material for electrochemical sensor and supercapacitor applications. As expected, the GO@CoMoSe2 modified glassy carbon electrode exhibited an excellent electrocatalytic activity toward the sensing of Metol (LOD, 0.009 μM; sensitivity, 2.397 μA μM–1 cm–2). Meanwhile, GO@CoMoSe2-coated nickel foam (NF) achieved feasible specific capacity (431.47 C g–1). In addition, the GO@CoMoSe2//AC asymmetric device exhibited the feasible energy density of 58.32 W h kg–1 at power density of 1800.25 W kg–1. Thus, we concluded that the Co doping and GO hybridization with MoSe2 provide the interesting idea to find out the excellent electrocatalysts with improved electrochemical performances toward the sensing and battery type supercapacitor applications.
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