Electrical Engineering Division, Department of Engineering, University of Cambridge , 9 J. J. Thomson Avenue, CB3 0FA Cambridge, U.K.
Faculty of Physics, University of Vienna , Boltzmanngasse 5, A 1090 Vienna, Austria.
ACS Nano. 2016 Jan 26;10(1):747-54. doi: 10.1021/acsnano.5b05819. Epub 2015 Dec 31.
The contribution of subnanometer pores in carbon electrodes to the charge-storage mechanism in supercapacitors has been the subject of intense debate for over a decade. Here, we provide a model system based on graphene oxide, which employs interlayer constrictions as a model for pore sizes that can be both controllably tuned and studied in situ during supercapacitor device use. Correlating electrochemical performance and in situ tuning of interlayer constrictions, we observe a peak in specific capacitance when interlayer constriction size reaches the diameters of unsolvated ions, supporting the hypothesized link between loss of ion solvation shell and anomalous capacitance increase for subnanometer pores.
碳电极中亚纳米孔对超级电容器电荷存储机制的贡献已经成为过去十年激烈争论的话题。在这里,我们提供了一个基于氧化石墨烯的模型系统,该系统采用层间收缩作为可控制调节的孔尺寸模型,并可在超级电容器器件使用过程中进行原位研究。通过关联电化学性能和层间收缩的原位调节,当层间收缩尺寸达到未溶剂化离子的直径时,我们观察到比电容出现峰值,这支持了亚纳米孔中离子溶剂化壳的损失与异常电容增加之间的假设联系。