Aliaa M. Salem , Sayed Y. Attia , Amira Gaber , Saad G. Mohamed , Soliman I. El-Hout
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引用次数: 0
摘要
PANI 具有弹性高、比电容大、氧化态多和价格相对便宜等特点,在能源系统的转换和储存方面具有相当大的潜力。遗憾的是,PANI 的稳定性较差,限制了它的使用。PANI 与其他活性材料的耦合有望克服 PANI 固有的局限性。在这里,我们成功合成了还原氧化石墨烯(rGO),并将其用作碳基底,在不同的工作温度(0°C、室温(RT)和 50°C)下对 PANI 进行原位化学聚合。制备的 PANI-RT/rGO 纳米复合材料具有高孔隙率和高比表面积,是离子扩散的通道。在外加电流为 2 A.g-1 时,所制备的 PANI-RT、PANI-50、PANI-0 和 PANI-RT/rGO 电极的估计电化学结果分别为 832 F.g-1(418 C/g)、256 F.g-1(128 C/g)、224 F.g-1(112 C/g)和 1056 F.g-1(528 C/g)。PANI-RT/rGO 电极的电容远大于其他电极,rGO 的加入是提高电化学存储能力的关键因素。此外,该装置非常稳定,在 5 A g-1 下反复运行 3 K 充放电后,仍能保持 90% 的原始容量。
PANI exhibited considerable potential in the conversion and storage of energy systems because of its high elasticity, large specific capacitance, multiple oxidation states, and relatively inexpensive. Unfortunately, PANI's poor stability restricts its usage. The coupling of PANI and other active materials has the potential to overcome PANI's inherent limitations. Here, we successfully synthesized reduced graphene oxide (rGO) that was utilized as a carbon substrate for in situ chemical polymerization of PANI at different operating temperatures [0°C, room temperature (RT), and 50°C]. The fabricated PANI-RT/rGO nanocomposite showed a high porosity with a high surface area, acting as an ions diffusion pathway. The estimated electrochemical results of the prepared electrodes, PANI-RT, PANI-50, PANI-0, and PANI-RT/rGO electrodes at an applied current of 2 A.g−1 are 832 F.g−1 (418 C/g), 256 F.g−1 (128 C/g), and 224 F.g−1 (112 C/g), and 1056 F.g−1 (528 C/g), respectively. The capacitance of the PANI-RT/rGO electrode is much larger than that of the others, and rGO incorporation demonstrates a key factor in improving the electrochemical storage capability. Furthermore, the device is stable, keeping 90 % of its original capacity following 3 K charge/discharge repeated runs at 5 A g−1.
期刊介绍:
This journal is an international medium for the rapid publication of original research papers, short communications and subject reviews dealing with research on and applications of electronic polymers and electronic molecular materials including novel carbon architectures. These functional materials have the properties of metals, semiconductors or magnets and are distinguishable from elemental and alloy/binary metals, semiconductors and magnets.