用户名: 密码: 验证码:
Solvent Effect on the Pore-Size Dependence of an Organic Electrolyte Supercapacitor
详细信息    查看全文
  • 作者:De-en Jiang ; Zhehui Jin ; Douglas Henderson ; Jianzhong Wu
  • 刊名:The Journal of Physical Chemistry Letters
  • 出版年:2012
  • 出版时间:July 5, 2012
  • 年:2012
  • 卷:3
  • 期:13
  • 页码:1727-1731
  • 全文大小:278K
  • 年卷期:v.3,no.13(July 5, 2012)
  • ISSN:1948-7185
文摘
Organic electrolytes such as tetraethylammonium tetrafluoroborate dissolved in acetonitrile (TEA-BF4/ACN) are widely used in commercial supercapacitors and academic research, but conflicting experimental results have been reported regarding the dependence of surface-area-normalized capacitance on the pore size. Here we show from a classical density functional theory the dependence of capacitance on the pore size from 0.5 to 3.0 nm for a model TEA-BF4/ACN electrolyte. We find that the capacitance鈥損ore size curve becomes roughly flat after the first peak around the ion diameter, and the peak capacitance is not significantly higher than the large-pore average. We attribute the invariance of capacitance with the pore size to the formation of an electric double-layer structure that consists of counterions and highly organized solvent molecules. This work highlights the role of the solvent molecules in modulating the capacitance and reconciles apparently conflicting experimental reports.

Keywords:

authors" href="http://pubs.acs.org/action/doSearch?action=search&searchText=supercapacitors&qsSearchArea=searchText">supercapacitors; authors" href="http://pubs.acs.org/action/doSearch?action=search&searchText=organic+electrolytes&qsSearchArea=searchText">organic electrolytes; authors" href="http://pubs.acs.org/action/doSearch?action=search&searchText=electric+double+layers&qsSearchArea=searchText">electric double layers; authors" href="http://pubs.acs.org/action/doSearch?action=search&searchText=density+functional+theory&qsSearchArea=searchText">density functional theory

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700