Department of Mechanical Engineering and the Materials Science and Engineering Program, The University of Texas at Austin, One University Station C2200, Austin, Texas 78712, USA.
Nano Lett. 2012 Apr 11;12(4):1806-12. doi: 10.1021/nl203903z. Epub 2012 Mar 13.
We present a novel method to prepare highly conductive, free-standing, and flexible porous carbon thin films by chemical activation of reduced graphene oxide paper. These flexible carbon thin films possess a very high specific surface area of 2400 m(2) g(-1) with a high in-plane electrical conductivity of 5880 S m(-1). This is the highest specific surface area for a free-standing carbon film reported to date. A two-electrode supercapacitor using these carbon films as electrodes demonstrated an excellent high-frequency response, an extremely low equivalent series resistance on the order of 0.1 ohm, and a high-power delivery of about 500 kW kg(-1). While higher frequency and power values for graphene materials have been reported, these are the highest values achieved while simultaneously maintaining excellent specific capacitances and energy densities of 120 F g(-1) and 26 W h kg(-1), respectively. In addition, these free-standing thin films provide a route to simplify the electrode-manufacturing process by eliminating conducting additives and binders. The synthetic process is also compatible with existing industrial level KOH activation processes and roll-to-roll thin-film fabrication technologies.
我们提出了一种通过还原氧化石墨烯纸的化学活化来制备高导电性、自支撑和柔性多孔碳薄膜的新方法。这些柔性碳薄膜具有非常高的比表面积 2400 m(2) g(-1),面内电导率高达 5880 S m(-1)。这是迄今为止报道的自支撑碳膜的最高比表面积。使用这些碳薄膜作为电极的双电极超级电容器表现出优异的高频响应,极低的等效串联电阻(约 0.1 欧姆)和高达约 500 kW kg(-1)的高功率输出。虽然已经报道了更高频率和更高功率的石墨烯材料,但这些是在同时保持优异的比电容和能量密度分别为 120 F g(-1)和 26 W h kg(-1)的情况下实现的最高值。此外,这些自支撑的薄膜为简化电极制造工艺提供了一种途径,无需添加导电添加剂和粘合剂。该合成工艺还与现有的工业级 KOH 活化工艺和卷对卷薄膜制造技术兼容。