One goal of researchers focusing on lithium-ion batteries for electric vehicles is to decrease the time required for charging. This can be done by several methods, including increasing the electrolyte transport properties. Methyl acetate, used as a co-solvent in the electrolyte, has been shown by a number of researchers to increase cell rate capability dramatically but careful considerations of the impact of methyl acetate on cell lifetime have not been published to our knowledge. The impacts of methyl acetate as a co-solvent in NMC532/ graphite cells were systematically studied in this work. Ex-situ gas evolution measurements, electrochemical impedance spectroscopy, high rate charging tests, ultra-high precision coulometry, isothermal microcalorimetry and long term cycling at both 20 and 40 • C were used to probe the impacts of including methyl acetate as a co-solvent. This work will be of great interest to Li-ion battery scientists developing cells that can support rapid charge and still maintain long lifetime. Lithium ion cells for electric vehicles should have long lifetime, high energy density and be able to support high rate charging. If cells are charged too rapidly for a given temperature, it is possible that unwanted lithium plating on the graphite negative electrode can occur and can accelerate cell capacity loss.1 There are a number of factors that influence the ability of cells to be charged rapidly. These include the thicknesses of the electrodes and the separator, the porosity and tortuosity of the electrodes and the separator and the electrolyte transport properties. In addition, Liu et al.,2 recently highlighted the importance of the negative electrode solid electrolyte interphase (SEI) resistance on the ability of cells to be charged rapidly without unwanted lithium plating during charge.For any given cell design, the easiest change to make in Liion cell manufacturing is a change in the electrolyte. All that entails, apart from possible materials compatibility issues, is filling cells with a different fluid. Electrolytes that promote high lithiumion diffusion constants, low viscosity, high conductivity, a high lithium ion transference number and promote low resistance negative electrode SEI layers are preferred for cells designed for high rate charging. Esters are beneficial co-solvents that lower freezing points, increase ionic conductivity and lower viscosity. Esters have been applied to improve the low temperature rate capability of Liion cells and also improve rate capability at room temperature. [3][4][5][6][7][8][9][10] Li-ion batteries with esters and positive electrodes of LiCoO 2 were studied in References 4-7 while those with LiNi x Co 1-x O 2 positive electrodes were studied by Smart et al. lifetime with an electrolyte containing 2 wt% prop-1-ene-1,3 sultone (PES) + 1 wt% tris (trimethylsilyl) phosphite (TTSPi) + 1 wt % ethylene sulfate (DTD) in 1 M LiPF 6 in ethylene carbonate (EC): ethyl methyl carbonate (EMC) (3:7 by weight). More than 92% capacity was maintained after testing for ...