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Effect of synthesis route on the electrochemical performance of CoMnFeO_4 nanoparticles as a novel supercapacitor electrode material

机译:合成途径对新型超级电容器电极材料CoMnFeO_4纳米粒子电化学性能的影响

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In this study, CoMnFeO4 ternary metal oxide nanoparticles are prepared via hydrothermal and sol-gel ignition methods. Their structures are investigated and characterized by FT-IR, XRD, XPS, BET, SEM, EDX and HR-TEM analysis. Also, magnetic properties of nanoparticles synthesized by two methods are compared on a vibrant sample magnetometer (VSM) with maximum saturation magnetization values found to be 28.83 emu g(-1) and 23.17 emu g(-1), respectively. SEM and HR-TEM results reveal that the mean particles size of hydrothermally synthesized (about 25 nm) nanoparticles is smaller and more uniform than that of their counterparts synthesized by sol-gel ignition method (about 65 nm). Their supercapacitor behaviors are studied and compared by cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS) methods. The hydrothermally synthesized sample shows higher specific capacitance of about 770 F g(-1) (at 1 A g(-1)) in 3M KOH while this value for the sample synthesized by sol-gel ignition approach is about 150 F g(-1). The higher specific capacitance can be attributed to smaller particle size, more electroactive sites due to higher specific surface area, and quantum size effects. Also, some initial mechanistic studies are performed to achieve a deeper insight into the electrochemical behavior of the nanoparticles implying that the oxidation-reduction process of nanoparticles is generally quasi-reversible and diffusion-controlled. So, by considering the higher performance, the hydrothermal approach developed here is beneficial from cost, time and environmental points of view.
机译:在这项研究中,CoMnFeO4三元金属氧化物纳米粒子是通过水热和溶胶-凝胶点火方法制备的。通过FT-IR,XRD,XPS,BET,SEM,EDX和HR-TEM分析对它们的结构进行了研究和表征。此外,在充满活力的样品磁强计(VSM)上比较了通过两种方法合成的纳米颗粒的磁性,最大饱和磁化强度分别为28.83 emu g(-1)和23.17 emu g(-1)。 SEM和HR-TEM结果表明,水热合成的纳米粒子(约25 nm)比通过溶胶-凝胶点火法合成的纳米粒子(约65 nm)更小,更均匀。通过循环伏安法(CV),恒电流充放电(GCD)和电化学阻抗谱(EIS)方法研究和比较了它们的超级电容器性能。水热合成样品在3M KOH中显示出约770 F g(-1)(在1 A g(-1)时)更高的比电容,而通过溶胶-凝胶点火方法合成的样品的该比值约为150 F g(- 1)。较高的比电容可归因于较小的粒径,由于较高的比表面积而产生的更多电活性位点以及量子尺寸效应。同样,进行了一些初步的机理研究,以更深入地了解纳米粒子的电化学行为,这暗示着纳米粒子的氧化还原过程通常是准可逆的且受扩散控制的。因此,考虑到更高的性能,从成本,时间和环境角度来看,这里开发的水热方法是有益的。

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