D.C. Pawar, D.B. Malavekar, J.H. Kim, C.D. Lokhande
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引用次数: 0
Abstract
As electrochemical energy storage systems become more prevalent, there is a growing imperative to investigate electrode materials that offer both flexibility and superior capacitive performance. In this research, a stainless steel substrate was used to synthesize a composite of reduced graphene oxide/polypyrrole (rGO/Ppy) by simple successive ionic layer adsorption and reaction (SILAR) method. The various rGO concentrations were used to improve the material electrochemical characteristics. Field emission scanning electron microscopy images revealed that Ppy particles were sandwiched between rGO sheets. At a 1 mg mL−1 of rGO concentration, the highest specific capacitance of rGO/Ppy composite was 803 F g−1, greater than Ppy (331 F g−1). The rGO/Ppy composite exhibited remarkable cycling stability, retaining over 92% of its initial capacitance over 5,000 cycles. Furthermore, rGO/Ppy/PVA-H2SO4/WO3 flexible solid- state supercapacitor device revealed a specific capacitance of 49 F g−1 at 5 mV s−1 scan rate and showed a maximum specific energy (SE) of 12 Wh kg−1 at a 881 W kg−1 specific power (SP). This indicates that the optimized concentration of rGO in Ppy composite led to an improvement in capacitive performance, and SILAR proved to be an effective method for preparing composite electrodes.
随着电化学储能系统的日益普及,研究既能提供柔性又能提供优越电容性能的电极材料变得越来越迫切。本研究以不锈钢为基体,采用简单连续离子层吸附反应(SILAR)法制备了还原性氧化石墨烯/聚吡咯(rGO/Ppy)复合材料。采用不同浓度的还原氧化石墨烯来改善材料的电化学特性。场发射扫描电镜图像显示,Ppy颗粒被夹在氧化石墨烯薄片之间。在rGO浓度为1 mg mL−1时,rGO/Ppy复合材料的最高比电容为803 F g−1,大于Ppy的331 F g−1。rGO/Ppy复合材料表现出显著的循环稳定性,在5000次循环中保持了92%以上的初始电容。rGO/Ppy/PVA-H2SO4/WO3柔性固态超级电容器器件在5 mV s−1扫描速率下的比电容为49 F g−1,在881 W kg−1比功率(SP)下的最大比能(SE)为12 Wh kg−1。这表明优化后的氧化石墨烯在Ppy复合材料中的浓度导致了电容性能的提高,SILAR被证明是制备复合电极的有效方法。
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.