Department of Chemical System Engineering, School of Engineering, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo, 113-8656, Japan.
CD-FMat, National Institute of Advanced Industrial Science and Technology (AIST), Umezono 1-1-1, Tsukuba, Ibaraki, 305-8568, Japan.
Nat Commun. 2019 Feb 20;10(1):850. doi: 10.1038/s41467-019-08789-8.
Electric double-layer capacitors are efficient energy storage devices that have the potential to account for uneven power demand in sustainable energy systems. Earlier attempts to improve an unsatisfactory capacitance of electric double-layer capacitors have focused on meso- or nanostructuring to increase the accessible surface area and minimize the distance between the adsorbed ions and the electrode. However, the dielectric constant of the electrolyte solvent embedded between adsorbed ions and the electrode surface, which also governs the capacitance, has not been previously exploited to manipulate the capacitance. Here we show that the capacitance of electric double-layer capacitor electrodes can be enlarged when the water molecules are strongly confined into the two-dimensional slits of titanium carbide MXene nanosheets. Using electrochemical methods and theoretical modeling, we find that dipolar polarization of strongly confined water resonantly overscreens an external electric field and enhances capacitance with a characteristically negative dielectric constant of a water molecule.
双电层电容器是一种高效的储能设备,有望满足可持续能源系统中不均匀的电力需求。早期提高双电层电容器不理想电容的尝试集中在介观或纳米结构上,以增加可及表面积并最小化吸附离子与电极之间的距离。然而,吸附离子与电极表面之间嵌入的电解质溶剂的介电常数(也控制着电容)以前并未被利用来操纵电容。在这里,我们表明当水分子被强烈限制在碳化钛 MXene 纳米片的二维狭缝中时,双电层电容器电极的电容可以增大。我们使用电化学方法和理论建模发现,强烈受限水的偶极极化共振地屏蔽了外部电场并增强了电容,其特征是水分子的负介电常数。