超级电容器
二硒醚
石墨烯
电容
锰
材料科学
氧化物
电化学
电极
杂质
过渡金属
化学工程
纳米技术
无机化学
硒
化学
催化作用
冶金
物理化学
工程类
生物化学
有机化学
作者
B. Balamuralitharan,S. N. Karthick,Suresh Kannan Balasingam,Hemalatha Kuzhandaivel,Samayanan Selvam,J. Anandha Raj,Kandasamy Prabakar,Yongseok Jun,Hee‐Je Kim
标识
DOI:10.1002/ente.201700097
摘要
Abstract The integration of 2 D graphene nanosheets and layered transition‐metal dichalcogenides has been recognized as one of the most extensive strategies for the synthesis of promising electrode materials for energy‐storage devices. In this study, cubic manganese diselenide (MnSe 2 ) and hybrid reduced graphene oxide/MnSe 2 (G‐MnSe 2 ) materials were synthesized by a facile hydrothermal method. Metallic selenium impurities are considered to be a major unwanted byproduct in this method. An effective means to remove such bulk chalcogenides is a key challenge. For the synthesis of the G‐MnSe 2 hybrid material, we used a strategy in which the graphene oxide was mixed with manganese and selenium precursors. Surprisingly, the final G‐MnSe 2 product contained a negligible amount of selenium impurity. The MnSe 2 and G‐MnSe 2 hybrid materials were characterized in detail. For the first time, the electrochemical energy‐storage behavior of MnSe 2 ‐based materials was assessed for supercapacitor applications. The specific capacitance of the MnSe 2 electrode was approximately 57.8 mF cm −2 , whereas the hybrid G‐MnSe 2 electrode showed a much higher specific capacitance of 93.3 mF cm −2 at a scan rate of 1 mV s −1 . A symmetric cell made from the G‐MnSe 2 hybrid material showed excellent long‐term stability for 4500 cycles and approximately 106 % retention of its initial capacitance, which is impressive compared with the cycle life of the MnSe 2 ‐based symmetric cell (80 % capacitance retention at the 4500th cycle).
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