Li-ion Battery Recycling by Energy-Efficient, High Throughput Li2SO4 Salt Splitting in a Diaphragm Flow Cell

24 November 2025, Version 1
This content is an early or alternative research output and has not been peer-reviewed by Cambridge University Press at the time of posting.

Abstract

Rapidly growing demand for lithium-ion batteries (LIBs) necessitates a significant expansion of LIB recycling to ensure adequate supply and reduce environmental burdens. Traditional hydrometallurgical LIB recycling processes use superstoichiometric quantities of acid and base and generate large volumes of salt waste. Electrochemical regeneration of acid and base from salt offers a zero-waste alternative but faces challenges with respect to throughput and energy consumption. This study reports a hydrometallurgical process to recycle lithium cobalt oxide (LCO) and lithium nickel manganese cobalt oxide (NMC) cathodes using acid and base electrochemically generated from a Li2SO4 electrolyte. The electrochemical cell used contains no ion exchange membranes, enabling excellent energy efficiency between 0.033 - 0.097 kWh/mol at current densities up to 500 mA/cm2 and imparting a robust tolerance for impurities that typically foul IEMs. The produced acid and base are found to be competent for etching and recovering >90% of the valuable metals from LIBs at industrially relevant pulp densities up to 66 g/L, and are readily regenerated from the salt solution left at the end of the metal recovery process.

Keywords

Li-ion Battery Recycling
Hydrometallurgy
Salt Splitting

Supplementary materials

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Supplementary Information
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Supporting Methods for chemicals employed, characterization techniques (pXRD, ICP-OES, Titrations, pH measurement), leaching experiments, precipitation experiments, cell assembly, electrochemical measurements, current efficiency measurements. Supporting Notes regarding reaction stoichiometry, alkaline error. Supporting Figures on pH changes, LSVs of DFC, charge transport in the DFC by species identity, picture of hydrogen peroxide decomposition, pH change during Li2CO3 precipitation, pXRD of variously washed Li2CO3, photos of leachate precipitates. Supporting Tables for DFC performance metrics, DFC output speciation and pH, residual concentration of transition metals, data for Figure 4B (PDF)
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