Mahmoudi-Qashqay Samaneh, Zamani-Meymian Mohammad-Reza, Maleki Ali
Department of Physics, Iran University of Science and Technology, P.O. Box 16846-13114, Tehran, Iran.
Catalysts and Organic Synthesis Research Laboratory, Department of Chemistry, University of Science and Technology, 16846-13114, Tehran, Iran.
Sci Rep. 2024 Nov 24;14(1):29105. doi: 10.1038/s41598-024-80243-2.
The increasing need for electrode materials exhibiting improved performance to meet the requirements of supercapacitors is on the rise. Hybrid electrodes, which combine reduced graphene oxide (rGO) with transition metal-based oxides, have emerged as promising materials due to their impressive specific capacitance and cost-effectiveness, attributed to their synergistic properties. In the present study, a binder-free CoOrGO composite electrode was synthesized using a facile, fast, and simple one-step co-precipitation method. This was done to improve both capacity and stability for supercapacitor applications. The composite materials underwent comprehensive characterization utilizing various surface analytical techniques, including X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), field-emission scanning electron microscopy (FE-SEM), fourier-transform infrared spectroscopy (FTIR), and Brunauer-Emmett-Teller (BET) analysis. Electrochemical measurements of the CoOrGO composite revealed at current density of 2 A cm a specific capacitance of 132.3 mF cm, with an impressive 95.91% retention of capacitance after 7000 cycles. The results from electrochemical impedance spectroscopy (EIS) highlighted a meager low relaxation time constant of 0.53 s for the composite films. The reason behind this can be linked to the synergistic interactions, and minimal charge transfer resistance exhibited by the porous electrode without binders. Based on the obtained results, this work introduces a flexible methodology for crafting advanced energy storage systems. This demonstrates the potential for designing high-efficiency supercapacitors that are suitable for a broad range of large-scale applications.
对具有改进性能以满足超级电容器要求的电极材料的需求日益增长。将还原氧化石墨烯(rGO)与过渡金属基氧化物相结合的混合电极,由于其令人印象深刻的比电容和成本效益,凭借其协同特性已成为有前途的材料。在本研究中,采用简便、快速且简单的一步共沉淀法合成了无粘合剂的CoOrGO复合电极。这样做是为了提高超级电容器应用的容量和稳定性。利用各种表面分析技术对复合材料进行了全面表征,包括X射线衍射(XRD)、能量色散X射线光谱(EDS)、场发射扫描电子显微镜(FE-SEM)、傅里叶变换红外光谱(FTIR)和布鲁诺尔-埃米特-泰勒(BET)分析。CoOrGO复合材料的电化学测量结果表明,在电流密度为2 A cm时,比电容为132.3 mF cm,在7000次循环后电容保持率高达95.91%。电化学阻抗谱(EIS)的结果突出显示,复合膜的低弛豫时间常数仅为0.53 s。其背后的原因可归因于协同相互作用以及无粘合剂的多孔电极表现出的最小电荷转移电阻。基于所得结果,这项工作引入了一种灵活的方法来制造先进的储能系统。这证明了设计适用于广泛大规模应用的高效超级电容器的潜力。