Maruthasalamoorthy Selvan, Rangaswamy Navamathavan
Department of Physics, School of Advanced Sciences, Vellore Institute of Technology (VIT) Chennai, Vandalur - Kelambakkam Road, Chennai 600127, India.
ACS Omega. 2024 Dec 17;9(52):51481-51493. doi: 10.1021/acsomega.4c08731. eCollection 2024 Dec 31.
Nickel pyrovanadate (NVO) and compositing rGO in different concentrations with NVO are synthesized via the solvothermal process. XRD patterns reveal the formation of crystalline NVO and amorphous rGO in the nanocomposite. The morphology of the material resembles the formation of an NVO hollow nanosphere through a template-free synthesis route with the effect of ethylene glycol. From the CV oxidation and reduction curve, the battery-type faradic reaction is observed. The specific surface area increment via the rGO concentration increment in nanocomposites is due to the partially encapsulated hollow sphere on the 2D active surface area of rGO owing to better specific capacitance and electrochemical stability. In addition, the maximum specific capacitance of 3807 F g at 1 A g for NVO@rGO 20 is obtained via a three-electrode system. The solid-state device shows the specific capacitance retention of ∼70% even after 10,000 cycles for a scan rate of 10 A g. The liquid electrolyte device shows the specific capacitance retention of ∼90% from its initial value and the successive charge-discharge process seen over the 10,000 cycles for the scan rate 10 A g. The suitable device is identified from this work in terms of high stability, high specific capacitance, and excellent reversibility for electrochemical performance.
通过溶剂热法合成了焦钒酸镍(NVO)以及不同浓度的NVO与rGO的复合材料。X射线衍射图谱揭示了纳米复合材料中结晶态NVO和非晶态rGO的形成。该材料的形态类似于通过无模板合成路线并在乙二醇作用下形成的NVO空心纳米球。从循环伏安氧化和还原曲线可以观察到电池型法拉第反应。纳米复合材料中随着rGO浓度增加比表面积增大,这是由于rGO二维活性表面积上部分包裹的空心球具有更好的比电容和电化学稳定性。此外,通过三电极系统在1 A g时NVO@rGO 20的最大比电容为3807 F g。固态器件在扫描速率为10 A g的情况下,即使经过10000次循环,比电容保持率仍约为70%。液体电解质器件在扫描速率为10 A g的10000次连续充放电过程中,比电容从初始值保持约90%。从这项工作中确定了该合适器件在电化学性能方面具有高稳定性、高比电容和优异的可逆性。