No abstract

No abstract

The synthesis of promising nanocomposite materials can always be tricky and depends a lot on the method of synthesis itself. Developing such synthesis routes, which are not only simple but also can effectively catch up the synergy of the compositing material, is definitely a worthy contribution towards nanomaterial science. Carbon-based materials, such as graphene oxide, and conjugative polymers, such as conductive polyaniline, are considered materials of the 21st century. This study involves a simple one pot synthesis route for obtaining a nanocomposite of polyaniline and graphene oxide with synergistic effects. The study was carried out in a systematic way by gradually changing the composition of the ingredients in the reaction bath until the formation of nanocomposite took place at some particular reaction parameters. These nanocomposites were then utilized for the fabrication of electrodes for aqueous symmetric supercapacitor devices utilizing gold or copper as current collectors. The device manifested a good capacitance value of 264 F/g at 1 A/g, magnificent rate performance, and capacitance retention of 84.09% at a high current density (10 A/g) when gold sheet electrodes were used as the current collectors. It also showed a capacitance retention of 79.83% and columbic efficiency of 99.83% after 2000 cycles.

No abstract

Conducting polymers and carbon-based materials such as graphene oxide (GO) and activated carbon (AC) are the most promising capacitive materials, though both offer charge storage through different mechanisms. However, their combination can lead to some unusual results, offering improvement in certain properties in comparison with the individual materials. Cycling stability of supercapacitors devices is often a matter of concern, and extensive research is underway to improve this phenomena of supercapacitive devices. Herein, a high-performance asymmetric supercapacitor device was fabricated using graphene oxide–polyaniline (GO@PANI) nanocomposite as positive electrode and activated carbon (AC) as negative electrode. The device showed 142 F g−1 specific capacitance at 1 A g−1 current density with capacitance retention of 73.94% at higher current density (10 A g−1). Most importantly, the device exhibited very high electrochemical cycling stability. It retained 118.6% specific capacitance of the starting value after 10,000 cycles at 3 Ag−1 and with coulombic efficiency of 98.06 %, indicating great potential for practical applications. Very small solution resistance (Rs, 0.640 Ω) and charge transfer resistance (Rct, 0.200 Ω) were observed hinting efficient charge transfer and fast ion diffusion. Due to asymmetric combination, potential window was extended to 1.2 V in aqueous electrolyte, as a result higher energy density (28.5 Wh kg−1) and power density of 2503 W kg−1 were achieved at the current density 1 Ag−1. It also showed an aerial capacitance of 57 mF cm−2 at current 3.2 mA cm−2. At this current density, its energy density was maximum (0.92 mWh cm−2) with power density (10.47 W cm−2).