TY - JOUR
T1 - Analysis of Vinylene Carbonate (VC) as additive in graphite/LiNi0.5Mn1.5O4 cells
AU - Pritzl, Daniel
AU - Solchenbach, Sophie
AU - Wetjen, Morten
AU - Gasteiger, Hubert A.
N1 - Publisher Copyright:
© The Author(s) 2017. Published by ECS. All rights reserved.
PY - 2017
Y1 - 2017
N2 - Vinylene Carbonate (VC) is an effective electrolyte additive to produce a stable solid electrolyte interphase (SEI) on graphite anodes, increasing the capacity retention of lithium-ion cells. However, in combination with LiNi0.5Mn1.5O4 (LNMO) cathodes, VC drastically decreases cell performance. In this study we use on-line electrochemical mass spectrometry (OEMS) and electrochemical impedance spectroscopy (EIS) with a micro-reference electrode to understand the oxidative (in-)stability of VC and its effect on the interfacial resistances of both anode and cathode. We herein compare different VC concentrations corresponding to VC to graphite surface area ratios typically used in commercial-scale cells. At low VC concentrations (0.09 wt%, corresponding to 1 wt% in commercial-scale cells), an impedance increase exclusively on the anode and an improved capacity retention is observed, whereas higher VC concentrations (0.17 wt – 2 wt%, corresponding to 2 wt - 23 wt% in commercial-scale cells) show an increase in both cathode and anode impedance as well as worse cycling performance and overcharge capacity during the first cycle. By considering the onset potentials for VC reduction and oxidation in graphite/LNMO cells, we demonstrate that low amounts of VC can be reduced before VC oxidation occurs, which is sufficient to effectively passivate the graphite anode.
AB - Vinylene Carbonate (VC) is an effective electrolyte additive to produce a stable solid electrolyte interphase (SEI) on graphite anodes, increasing the capacity retention of lithium-ion cells. However, in combination with LiNi0.5Mn1.5O4 (LNMO) cathodes, VC drastically decreases cell performance. In this study we use on-line electrochemical mass spectrometry (OEMS) and electrochemical impedance spectroscopy (EIS) with a micro-reference electrode to understand the oxidative (in-)stability of VC and its effect on the interfacial resistances of both anode and cathode. We herein compare different VC concentrations corresponding to VC to graphite surface area ratios typically used in commercial-scale cells. At low VC concentrations (0.09 wt%, corresponding to 1 wt% in commercial-scale cells), an impedance increase exclusively on the anode and an improved capacity retention is observed, whereas higher VC concentrations (0.17 wt – 2 wt%, corresponding to 2 wt - 23 wt% in commercial-scale cells) show an increase in both cathode and anode impedance as well as worse cycling performance and overcharge capacity during the first cycle. By considering the onset potentials for VC reduction and oxidation in graphite/LNMO cells, we demonstrate that low amounts of VC can be reduced before VC oxidation occurs, which is sufficient to effectively passivate the graphite anode.
UR - http://www.scopus.com/inward/record.url?scp=85032657457&partnerID=8YFLogxK
U2 - 10.1149/2.1441712jes
DO - 10.1149/2.1441712jes
M3 - Article
AN - SCOPUS:85032657457
SN - 0013-4651
VL - 164
SP - A2625-A2635
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 12
ER -