TY - JOUR
T1 - Li-Ion Battery Active Material Impedance Analysis I
T2 - Comparison of Measured NCM 111 Kinetics with Butler-Volmer Equation Based Predictions
AU - Morasch, Robert
AU - Gasteiger, Hubert A.
AU - Suthar, Bharatkumar
N1 - Publisher Copyright:
© 2023 The Author(s). Published on behalf of The Electrochemical Society by IOP Publishing Limited
PY - 2023/8/1
Y1 - 2023/8/1
N2 - The expression for the exchange current density to describe the intercalation kinetics of Li-ion battery materials proposed by Newman and coworkers has been used extensively for battery modeling, however its applicability to existing battery materials should be validated. Here we show an electrochemical impedance spectroscopy (EIS) analysis of the kinetic behavior of NCM 111 as a function of electrolyte salt concentration and state-of-charge (SOC) and compare it to the proposed theory. An areal capacity dependent EIS analysis first gives insights into the feasibility of measuring kinetic and transport parameters, including the solid diffusion resistance of lithium, showing that low-areal capacity electrodes are required to predominantly probe the kinetics. We then show how the charge transfer kinetics follow a Butler-Volmer type concentration dependent behavior for lower concentrated electrolytes (≤1.5 M) but deviate from the proposed theory at higher salt concentrations. A further SOC dependent analysis shows how NCM 111 generally follows the proposed theory of U-shaped symmetric kinetics, but the limited oxidative stability window leads to practically asymmetric kinetics for charging and discharging. This asymmetry is visible in NCM 111 lithiation and delithiation rate tests, where upon lithiation the kinetics generally become slower for higher degrees of lithiation, limiting the performance.
AB - The expression for the exchange current density to describe the intercalation kinetics of Li-ion battery materials proposed by Newman and coworkers has been used extensively for battery modeling, however its applicability to existing battery materials should be validated. Here we show an electrochemical impedance spectroscopy (EIS) analysis of the kinetic behavior of NCM 111 as a function of electrolyte salt concentration and state-of-charge (SOC) and compare it to the proposed theory. An areal capacity dependent EIS analysis first gives insights into the feasibility of measuring kinetic and transport parameters, including the solid diffusion resistance of lithium, showing that low-areal capacity electrodes are required to predominantly probe the kinetics. We then show how the charge transfer kinetics follow a Butler-Volmer type concentration dependent behavior for lower concentrated electrolytes (≤1.5 M) but deviate from the proposed theory at higher salt concentrations. A further SOC dependent analysis shows how NCM 111 generally follows the proposed theory of U-shaped symmetric kinetics, but the limited oxidative stability window leads to practically asymmetric kinetics for charging and discharging. This asymmetry is visible in NCM 111 lithiation and delithiation rate tests, where upon lithiation the kinetics generally become slower for higher degrees of lithiation, limiting the performance.
UR - http://www.scopus.com/inward/record.url?scp=85170203647&partnerID=8YFLogxK
U2 - 10.1149/1945-7111/acf161
DO - 10.1149/1945-7111/acf161
M3 - Article
AN - SCOPUS:85170203647
SN - 0013-4651
VL - 170
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 8
M1 - 080522
ER -