孟长功

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:中科院金属所

学位:博士

所在单位:化工学院

学科:无机化学

办公地点:大连理工大学化学楼401

联系方式:13940825088

电子邮箱:cgmeng@dlut.edu.cn

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In-situ hydrothermal growth of Zn4Si2O7(OH)(2)center dot H2O anchored on 3D N, S-enriched carbon derived from plant biomass for flexible solid-state asymmetrical supercapacitors

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论文类型:期刊论文

发表时间:2018-11-15

发表刊物:CHEMICAL ENGINEERING JOURNAL

收录刊物:SCIE

卷号:352

页面范围:519-529

ISSN号:1385-8947

关键字:Biomass; Zinc silicate; Supercapacitor; Hierarchical pores; Electrochemical performance

摘要:Zinc silicates are an appealing feature for electrode materials in Li-ion battery owing to their layered structure providing a well-defined and facile Li ion transportation route. However, the poor conductivity of zinc silicates limits their wide application as electrode materials, and furthermore zinc silicates have not been explored to apply to supercapacitor. Herein, three-dimensional N, S-doped C-Zn4Si2O7(OH)(2)center dot H2O (3D C-ZnSi) have been developed by a hydrothermal process from a highly available and recyclable plant biomass - bamboo leaves, composed of organic compound and silica, for the application to supercapacitor. This is about zinc silicate first applied to supercapacitor. The as-prepared electrode materials have extensive pores inherited from biological structures of bamboo leaves, including micropores, mesopores and macropores. Owing to the existence of hierarchical pores, the single electrode presents excellent capacitance of 450 mF cm(-2) at 5 mV 5(-1), and excellent cyclic performance with the retention of 83% after 10,000 cycles. Furthermore, the as-assembled 3D C-ZnSi//activated carbon (3D C-ZnSi//AC) flexible solid-state asymmetric supercapacitor can achieve a maximum energy density of 0.69 Wh m(-2). Additionally, the device exhibits high cycle stability for 6900 cycles with the retention of 80%. This study shows the possibility for 3D N,S doped C-Zn4Si2O7(OH)(2)center dot H2O as one of the most promising candidates for high performance energy storage devices.