Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/41597
Title: Polymeric Backbone Eutectogel Electrolytes for High-Energy Lithium-Ion Batteries
Authors: KELCHTERMANS, An-Sofie 
JOOS, Bjorn 
DE SLOOVERE, Dries 
PAULUS, Andreas 
MERCKEN, Jonas 
MYLAVARAPU, Satish Kumar 
ELEN, Ken 
MARCHAL, Wouter 
Tesfaye, Alexander
Thompson, Travis
VAN BAEL, Marlies 
HARDY, An 
Issue Date: 2023
Publisher: AMER CHEMICAL SOC
Source: ACS Omega, 8 (40) , p. 36753 -36763
Abstract: This work introduces a polymeric backbone eutectogel (P-ETG) hybrid solid-state electrolyte with an N-isopropylacrylamide (NIPAM) backbone for high-energy lithium-ion batteries (LIBs). The NIPAM-based P-ETG is (electro)chemically compatible with commercially relevant positive electrode materials such as the nickel-rich layered oxide LiNi0.6Mn0.2Co0.2O2 (NMC622). The chemical compatibility was demonstrated through (physico)chemical characterization methods. The nonexistence (within detection limits) of interfacial reactions between the electrolyte and the positive electrode, the unchanged bulk crystallographic composition, and the absence of transition metal ions leaching from the positive electrode in contact with the electrolyte were demonstrated by Fourier transform infrared spectroscopy, powder X-ray diffraction, and elemental analysis, respectively. Moreover, the NIPAM-based P-ETG demonstrates a wide electrochemical stability window (1.5-5.0 V vs Li+/Li) and a reasonably high ionic conductivity at room temperature (0.82 mS cm(-1)). The electrochemical compatibility of a high-potential NMC622-containing positive electrode and the P-ETG is further demonstrated in Li|P-ETG|NMC622 cells, which deliver a discharge capacity of 134, 110, and 97 mAh g(-1) at C/5, C/2, and 1C, respectively, after 90 cycles. The Coulombic efficiency is >95% at C/5, C/2, and 1C. Hence, gaining scientific insights into the compatibility of the electrolytes with positive electrode materials that are relevant to the commercial market, like NMC622, is important because this requires going beyond the electrolyte design itself, which is essential to their practical applications.
Notes: Kelchtermans, AS; Hardy, A (corresponding author), Hasselt Univ, Inst Mat Res Imo Imomec, Mat Chem, DESINe Grp, B-3590 Diepenbeek, Belgium.; Hardy, A (corresponding author), IMEC Vzw, Div Imomec Associated Lab, B-3590 Diepenbeek, Belgium.; Kelchtermans, AS; Hardy, A (corresponding author), EnergyVille, B-3600 Genk, Belgium.
ansofie.kelchtermans@uhasselt.be; an.hardy@uhasselt.be
Document URI: http://hdl.handle.net/1942/41597
ISSN: 2470-1343
e-ISSN: 2470-1343
DOI: 10.1021/acsomega.3c03081
ISI #: 001074236500001
Rights: 2023 The Authors. Published by American Chemical Society. Open access CC-By-NC 4.0
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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