Effect of electronic spatial extents (ESE) of ions on overpotential of lithium ion capacitors
- Authors
- Xu, Fan; Lee, Chung Ho; Koo, Chong Min; Jung, Cheolsoo
- Issue Date
- 2014-01-01
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Citation
- ELECTROCHIMICA ACTA, v.115, pp.234 - 238
- Abstract
- The electronic spatial extent (ESE) of ions was defined as a major concept for assessing the cause of overpotential in the charging and discharging processes of a nanoporous activated carbon (AC) electrode. The performance degradation of AC/Li half-cells was caused by the overpotential, which was in discord with the electrolyte conductivity and ion size. Compared to the overpotential with the salt concentration, the AC/Li half-cell with a high concentration had a smaller overpotential, and its discharge patterns were similar to the curves obtained from the half-cells with a smaller ESE of BF4- ion. The ESE is a more realistic solution for determining the overpotential of the nanoporous capacitor, such as supercapacitor and Li ion capacitor, because its capacity is dependent on the electron density at the electric double layer of the capacitor electrode. (C) 2013 Elsevier Ltd. All rights reserved.
- Keywords
- ACTIVATED CARBON ELECTRODES; DOUBLE-LAYER CAPACITOR; POLYMER ELECTROLYTE; ENERGY; CELL; ACTIVATED CARBON ELECTRODES; DOUBLE-LAYER CAPACITOR; POLYMER ELECTROLYTE; ENERGY; CELL; Electronic spatial extent; Overpotential; Nanopore; Capacitor; Potential drop
- ISSN
- 0013-4686
- URI
- https://pubs.kist.re.kr/handle/201004/127240
- DOI
- 10.1016/j.electacta.2013.10.175
- Appears in Collections:
- KIST Article > 2014
- Files in This Item:
There are no files associated with this item.
- Export
- RIS (EndNote)
- XLS (Excel)
- XML
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.