A direct comparison of the cathode-electrolyte interface (CEI) generated on high-voltage LiNiMnO cathodes with three different lithium borate electrolyte additives, lithium bis(oxalato)borate (LiBOB), lithium 4-pyridyl trimethyl borate (LPTB), and lithium catechol dimethyl borate (LiCDMB), has been conducted. The lithium borate electrolyte additives have been previously reported to improve the capacity retention and efficiency of graphite/LiNiMnO cells due to the formation of passivating CEI. Linear sweep voltammetry (LSV) suggests that incorporation of the lithium borates into 1.2 M LiPF in EC/EMC (3/7) electrolyte results in borate oxidation on the cathode surface at high potential. The reaction of the borates on the cathode surface leads to an increase in impedance as determined by electrochemical impedance spectroscopy (EIS), consistent with the formation of a cathode surface film. Ex-situ surface analysis of the electrode via a combination of SEM, TEM, IR-ATR, XPS, and high energy XPS (HAXPES) suggests that oxidation of all borate additives results in deposition of a passivation layer on the surface of LiNiMnO which inhibits transition metal ion dissolution from the cathode. The passivation layer thickness increases as a function of additive structure LiCDMB > LPTB > LiBOB. The results suggest that the CEI thickness can be controlled by the structure and reactivity of the electrolyte additive.
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http://dx.doi.org/10.1021/acsami.7b01481 | DOI Listing |
Chem Commun (Camb)
December 2024
Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
Lithium borate and aluminate salts bearing a hexafluoroisopropoxy ligand have been prepared and investigated for use in lithium-ion batteries and Cu‖Li cells. Lithium aluminate salts have poorer air tolerance but Li[Al(hfip)] resulted in superior battery cycling, with lower overpotentials for plating and stripping in Cu‖Li cells.
View Article and Find Full Text PDFJ Chem Phys
October 2024
Materials Integration Laboratories, AGC Inc., Yokohama, Kanagawa 230-0045, Japan.
Lithium-ion conducting borate glasses are suitable for solid-state batteries as an interfacial material between a crystalline electrolyte and an electrode, thanks to their superior formability. Chlorine has been known to improve the electron conductivity of borate glasses as a secondary anion. To examine the impact of chlorine on lithium dynamics, molecular dynamics (MD) simulations were performed with a machine-learning interatomic potential (MLIP).
View Article and Find Full Text PDFSci Rep
July 2024
Serbian Academy of Sciences and Arts, Kneza Mihajla 35, Belgrade, 11000, Serbia.
The proposed exploitation of the Jadar Valley lithium/borate deposit in Serbia, by the Rio Tinto Corporation, indicates that it would become large-scale processing of boron- and lithium-containing ore. It would be one of the world's very first lithium mines in populated and agricultural area. The company claims that the envisioned mining will be in accordance with environmental protection requirements.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2024
Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK.
Improving composite cathode function is key to the success of the solid-state battery. Maximizing attainable cathode capacity and retention requires integrating suitable polymeric binders that retain a sufficiently high ionic conductivity and long-term chemo-mechanical stability of the cathode active material-solid-electrolyte-carbon mixture. Herein, we report block copolymer networks composed of lithium borate polycarbonates and poly(ethylene oxide) that improved the capacity (200 mAh g at 1.
View Article and Find Full Text PDFPhys Chem Chem Phys
May 2024
Philipps-Universität Marburg, Chemistry Department, Hans-Meerwein Str. 4, 35043 Marburg, Germany.
The potential energy landscape of lithium borate glass of composition LiBO has been investigated by the charge attachment induced transport (CAIT) technique. Here, native lithium ions have been replaced by foreign alkali ions, M = K, Rb, Cs. All experiments exhibit a pronounced decrease of native ion diffusion coefficients over more than 4 orders of magnitude with decreasing local population of Li.
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