Electrostatic self-assembly of MXene and edge-rich CoAl layered double hydroxide on molecular-scale with superhigh volumetric performances

电解质 超级电容器 阳极 单层 材料科学 电极 阴极 石墨烯 储能 异质结 纳米技术 电导率 氢氧化物 化学工程 电化学 光电子学 化学 有机化学 工程类 功率(物理) 物理化学 物理 量子力学
作者
Hao Niu,Xue Yang,Qian Wang,Xiaoyan Jing,Kui Cheng,Kai Zhu,Ke Ye,Guiling Wang,Dianxue Cao,Jun Yan
出处
期刊:Journal of Energy Chemistry [Elsevier BV]
卷期号:46: 105-113 被引量:109
标识
DOI:10.1016/j.jechem.2019.10.023
摘要

It is highly desirable to design and synthesize two-dimensional nanostructured electrode materials with high electrical conductivity, large electrolyte-accessible surface area and more exposed active sites for energy storage applications. Herein, MXene/CoAl-LDH heterostructure has been prepared through electrostatic ordered hetero-assembly of monolayer MXene and edge-rich CoAl-LDH nanosheets in a face-to-face manner on molecular-scale for supercapacitor applications. Benefiting from the unique structure, strong interfacial interaction and synergistic effects between MXene and CoAl-LDH nanosheets, the electrical conductivity and exposed electrolyte-accessible active sites are significantly enhanced. The as-prepared MXene/CoAl-LDH-80% (ML-80) film exhibits high volumetric capacity of 2472 C cm−3 in 3 M KOH electrolyte with high rate capability of 70.6% at 20 A g−1. Notably, to the best of our knowledge, the high volumetric capacity is the highest among other previously reported values for supercapacitors in aqueous electrolytes. Furthermore, our asymmetric supercapacitor device fabricated with ML-80 and MXene/graphene composite as cathode and anode, respectively, exhibits impressive volumetric energy density of 85.4 Wh L−1 with impressive cycling stability of 94.4% retention ratio after 30,000 continuous charge/discharge cycles.
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