z-logo
open-access-imgOpen Access
Electrochemical and Infrared Studies of the Reduction of Organic Carbonates
Author(s) -
Xuerong Zhang,
Robert Kostecki,
Thomas J. Richardson,
James K. Pugh,
Philip N. Ross
Publication year - 2001
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/1.1415547
Subject(s) - ethylene carbonate , electrolyte , dimethyl carbonate , cyclic voltammetry , electrochemistry , propylene carbonate , chemistry , inorganic chemistry , carbonate , glassy carbon , exfoliation joint , electrode , materials science , methanol , organic chemistry , nanotechnology , graphene
problematic due to co-intercalation of solvent molecules along with Li+ ion into the graphite and subsequent exfoliation 1. The electrolyte commonly used in commercial lithium-ion cells is based on ethylene carbonate (EC), even though these batteries have poorer low temperature performance.2 Research efforts have, with some success3,4, pursued additives to PC to generate a SEI layer that prevents PC co-intercalation. The mechanism of functioning of these additives is, however, still uncertain. We have performed quantum chemical calculations of the thermodynamic reduction potential of eleven organic molecules at an inert electrode assuming one-electron reduction.5 Here we report our experimental determinations of the reduction potentials of EC, PC, diethylcarbonate (DEC), dimethylcarbonate (DMC) and vinylene carbonate (VC), and compare them with calculated values. The role of VC as an additive was also investigated and the SEI layer resulting from its reduction characterized by infrared spectroscopy. EXPERIMENT

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom