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非对称离子液体电解质微分电容的平均场理论

A mean-field theory on the differential capacitance of asymmetric ionic liquid electrolytes.

作者信息

Han Yining, Huang Shanghui, Yan Tianying

机构信息

Tianjin Key Laboratory of Metal- and Molecule-Based Material Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Institute of New Energy Material Chemistry, College of Chemistry, Nankai University, Tianjin 300071, People's Republic of China.

出版信息

J Phys Condens Matter. 2014 Jul 16;26(28):284103. doi: 10.1088/0953-8984/26/28/284103. Epub 2014 Jun 12.

Abstract

The size of ions significantly influences the electric double layer structure of room temperature ionic liquid (IL) electrolytes and their differential capacitance (Cd). In this study, we extended the mean-field theory (MFT) developed independently by Kornyshev (2007J. Phys. Chem. B 111 5545-57) and Kilic, Bazant, and Ajdari (2007 Phys. Rev. E 75 021502) (the KKBA MFT) to take into account the asymmetric 1:1 IL electrolytes by introducing an additional parameter ξ for the anion/cation volume ratio, besides the ionic compressibility γ in the KKBA MFT. The MFT of asymmetric ions becomes KKBA MFT upon ξ = 1, and further reduces to Gouy-Chapman theory in the γ → 0 limit. The result of the extended MFT demonstrates that the asymmetric ILs give rise to an asymmetric Cd, with the higher peak in Cd occurring at positive polarization for the smaller anionic size. At high potential, Cd decays asymptotically toward KKBA MFT characterized by γ for the negative polarization, and characterized by ξγ for the positive polarization, with inverse-square-root behavior. At low potential, around the potential of zero charge, the asymmetric ions cause a higher Cd, which exceeds that of Gouy-Chapman theory.

摘要

离子的大小对室温离子液体(IL)电解质的双电层结构及其微分电容((C_d))有显著影响。在本研究中,我们扩展了由科尔尼舍夫(2007年,《物理化学杂志B》111卷,5545 - 557页)以及基利克、巴赞特和阿贾达里(2007年,《物理评论E》75卷,021502)独立发展的平均场理论(MFT)(KKBA MFT),通过在KKBA MFT中的离子压缩率(\gamma)之外,引入一个用于描述阴离子/阳离子体积比的附加参数(\xi),来考虑不对称的1:1离子液体电解质。当(\xi = 1)时,不对称离子的MFT变为KKBA MFT,并且在(\gamma \to 0)极限下进一步简化为古依 - 查普曼理论。扩展MFT的结果表明,不对称离子液体产生不对称的(C_d),对于较小的阴离子尺寸,(C_d)的较高峰值出现在正极化时。在高电位下,对于负极化,(C_d)渐近地衰减至以(\gamma)为特征的KKBA MFT,对于正极化,则以(\xi\gamma)为特征,呈现反平方根行为。在低电位下,在零电荷电位附近,不对称离子导致更高的(C_d),其超过了古依 - 查普曼理论的值。

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