Preparation and characterization of hexagonal mesoporous β-Co(OH)2 nanorings

被引:11
作者
Darbandi, Masih [1 ]
Shaabani, Behrouz [2 ]
Alizadeh, Arezoo [1 ,2 ]
Yardani, Pariya [3 ]
Shahryari, Elham [3 ]
Hosseini, Mir Ghasem [3 ]
机构
[1] Univ Tabriz, Fac Chem, Dept Phys Chem, Nanomat Res Lab, Tabriz, Iran
[2] Univ Tabriz, Fac Chem, Dept Inorgan Chem, Tabriz, Iran
[3] Univ Tabriz, Fac Chem, Dept Phys Chem, Electrochem Res Lab, Tabriz, Iran
关键词
Mesoporous; Cobalt hydroxide; Nanoring; Synthesis; Capacitance retention; LAYERED DOUBLE HYDROXIDE; OXIDE THIN-FILMS; COBALT HYDROXIDE; OXYGEN EVOLUTION; HIGH-PERFORMANCE; ELECTROCHEMICAL CAPACITANCE; CONTROLLABLE SYNTHESIS; SUPERCAPACITOR; CO(OH)(2); CO3O4;
D O I
10.1016/j.micromeso.2019.04.048
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Herein, a convenient and cost-effective approach carried out for the synthesis of hexagonal mesoporous beta-cobalt hydroxides nanorings via chemical precipitation. Transmission electron microscopic and X-ray diffraction results reveals that these nanorings mostly consist of beta-Co(OH)(2) with well crystalline hexagonal brucite like structure. The inert gas sorption-desorption measurements represents the mesoporous nature of the NPs. The Brunauer Emmett Teller surface area and average pore size of the as synthesized nanoparticles were about 210 m(2)/g and 5 nm. The especial mesoporous structures with excellent specific area are the reason for the good electrochemical capacitance performance and superior cyclic stability (only about 1% decay) in supercapacitor application. The as prepared nanoparticles have been used for oxygen evolution reaction. The oxygen evolution reaction performance is related to the active surface area of the nanoparticles due to the formation of mesoporous structure within the cobalt hydroxide nanoparticles. Furthermore, the presented facile synthetic process, which does not need any surfactant or template, could be extended to the preparation of other nanomaterials with excellent morphologies for supercapacitor and oxygen evolution reaction applications.
引用
收藏
页码:421 / 426
页数:6
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