Preparation and capacitance of MnO2 pillared Co2+-Ni2+-Fe3+ layered double hydroxide porous material supercapacitor

被引:10
|
作者
Yan, Zhe [1 ,2 ]
Dang, Qiao [1 ,2 ]
Lu, Yue [1 ,2 ]
Liu, Zong-Huai [1 ,2 ]
机构
[1] Shaanxi Normal Univ, Key Lab Appl Surface & Colloid Chem, Minist Educ, Xian 710010, Peoples R China
[2] Shaanxi Normal Univ, Sch Mat Sci & Engn, Xian 710010, Peoples R China
基金
中国国家自然科学基金;
关键词
Co2+-Ni2+-Fe3+ layered double hydroxides; MnO2; pillar; Porous material; Thermal stability; Specific capacitance; LITHIUM-OXYGEN BATTERIES; ELECTROCHEMICAL CAPACITOR; PHOTOCATALYTIC PROPERTIES; MESOPOROUS CARBON; MANGANESE OXIDE; ANION-EXCHANGE; ELECTRODE; CO; NANOSHEETS; COMPOSITE;
D O I
10.1016/j.colsurfa.2017.01.053
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
MnO2 pillared Co2+-Ni2+-Fe3+ layered double hydroxide nanocomposite with porous structure has been successfully prepared by using an intercalation/reduction reaction and followed by heating treatment. The structural evolution of the samples obtained at different stages are characterized by X-ray diffraction, field emission scanning electron microscopy, infrared spectroscopy, X-ray photoelectron spectroscopy, and N-2 adsorption-desorption analyses. MnO2 as a pillared agent can stabilize the layered structure against thermal treatment, and porous Co2+-Ni2+-Fe3+ layered double hydroxide nanocomposite is obtained by heating the MnO2 pillared material at appropriate temperatures. The basal spacing of the obtained intermediates changes with the radius of the pillar species in the interlayer and the layered structure with larger surface area can maintain to 300 degrees C. The as prepared MnO2-LDHs (200) material not only has large specific surface area of 145 m(2) g(-1), but also shows an ideal capacitance of 389 F g(-1) at a scan rate of 5 mV s(-1) and good capacitance retention of 92.3% after 500 cycles at a scan rate of 20 mV s(-1) in 1 mol L-1 KOH solution, making this material has a potential application as supercapacitor electrode material. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 38
页数:7
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