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Self-assembled amorphous manganese oxide/ hydroxide spheres via multi-phase electrochemical interactions in reverse micelle electrolytes and their capacitive behavior

机译:通过反胶束电解质中的多相电化学相互作用自组装的非晶锰氧化物/氢氧化物球及其电容行为

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摘要

Amorphous matrices of three-dimensionally interconnected MnO_x/MnOOH nano-spheres were electrochemically assembled onto a carbon substrate by a pulse galvanostatic method (PGM) in a nonionic reverse micelle electrolyte. The synthesized material showed a unique morphology which was attributed to a synergistic effect between the amphiphilic molecule based interface membrane as a soft template and the PGM approach. The transfer of the reactant was remarkably special because of the elusive thermodynamic and kinetic parameters of the interactions at the interface between the two different phases such as the polar phase-interface membrane, interface membrane-nonpolar phase and polar phase-electrode interactions. Further work involved investigations into the potential application of the assembled MnO_x/MnOOH films as high performance supercapacitor electrode materials. The capacitive performance of the assembled MnO_x/MnOOH was tested in a solution of 0.5 M Na2SO4. The highest specific discharge capacitance of 1659 F g~(-1) was achieved at a current density of 2 A g~(-1), and remained as high as 782 F g~(-1) even at a very large current density of 10 A g~(-1). The outstanding capacitance properties were ascribed to the ternary oxide composites forming highly porous nanostructures which guaranteed a large specific surface, full utilization of Mn oxides and a small amount of degradation of amorphous MnO2. The results indicate the feasibility of electrochemically synthesizing Mn oxides in unconventional micelle electrolytes, and their successful application in supercapacitors.
机译:将三维互连的MnO_x / MnOOH纳米球的非晶基质通过脉冲恒电流法(PGM)在非离子反胶束电解质中电化学组装到碳基底上。合成的材料显示出独特的形态,这归因于基于两亲分子的作为软模板的界面膜和PGM方法之间的协同作用。由于在两个不同相之间的界面上相互作用的难以捉摸的热力学和动力学参数,例如极性相界面膜,界面膜-非极性相和极性相-电极相互作用,反应物的转移是非常特殊的。进一步的工作涉及对组装好的MnO_x / MnOOH薄膜作为高性能超级电容器电极材料的潜在应用的研究。在0.5 M Na2SO4溶液中测试了组装好的MnO_x / MnOOH的电容性能。在2 A g〜(-1)的电流密度下可实现最高的1659 F g〜(-1)的比放电电容,即使在非常大的电流密度下也可保持高达782 F g〜(-1) 10 A g〜(-1)。杰出的电容性能归因于形成高度多孔纳米结构的三元氧化物复合物,该结构可确保大的比表面积,Mn氧化物的充分利用和非晶态MnO2的少量降解。结果表明,在非常规胶束电解质中电化学合成锰氧化物的可行性及其在超级电容器中的成功应用。

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