The effect of addition of Mn 2+ to the electrolyte on the lithiation of a model battery anode was studied using voltammetry, electrochemical quartz crystal microbalance (EQCM), scanning electron microscopy (SEM), Auger electron spectroscopy (AES) and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Cyclic voltammetry of a Au anode showed that the presence of one equivalent monolayer of Mn 2+ in the electrolyte reduces the battery capacity by as much as 48%, a result which is recapitulated in SEM images of the anode surface after five cycles which show that the presence of Mn 2+ blocks lithiation of the anode. AES demonstrates the presence or lack of Mn on the surface. EQCM analysis demonstrates greater initial mass gain on the anode with increasing concentration of Mn 2+ in the electrolyte while MALDI-TOF MS shows no observable differences in the solid electrolyte interface (SEI) between the electrolyte with or without Mn 2+ . The addition of Cu 2+ to the electrolyte exhibits an effect similar to Mn 2+ addition.Lithium ion batteries are a technology of great interest for applications in portable electronics and electric cars due to their high operating voltage and high energy density. LiMn 2 O 4 is a desirable cathode material for a lithium ion battery due to the low cost, environmentally benignity, thermal stability, and abundance. 1-4 However, batteries using LiMn 2 O 4 cathodes are subject to severe capacity fade with cycling. 3,4 This capacity fading is attributed to three main factors:(1) the instability of the electrolyte at high potentials when charging cells, (2) a Jahn-Teller distortion of the MnO 4 center at the discharged state, converting from a cubic symmetry to a tetragonal symmetry, reducing the stability of the cathode structure with cycling, and (3) the dissolution of Mn into the electrolyte. [5][6][7] The dissolution of Mn has been considered a vital issue to be solved to improve LiMn 2 O 4 cathodes. The amount of Mn dissolved into the electrolyte from a LiMn 2 O 4 cathode has been quantitatively analyzed by ion chromatography and concentrations up to 31 ppm Mn 2+ are found. 8 The dissolution of Mn may be enhanced with an increase of the concentration of acid, particularly HF forming from hydrolysis of LiPF 6 , in the electrolyte. 9 Prior research has examined the effect of Mn 2+ in the electrolyte. Mn dissolution reduces battery capacity by two methods: (1) material loss at the cathode 10,11 and (2) Mn reducing at the anode, causing an increase in cell resistance. 12-14 Mn reduction on the anode has been studied on graphite using EDS, XRD, AFM, XPS, and electrochemical impedance spectroscopy. 10,12,14,15 Additionally, a variety of methods have been used to reduce the effect of the dissolved Mn ions. These methods include adding inorganic electrolyte additives to prevent further reduction of Mn on the anode, 16,17 substituting a fraction of the Mn atoms with other transition metal atoms in the cathode, 18 and redepositing the Mn on the cathode before d...