In the pursuit of lowering the cost of lithium-ion (LIB) and lithium-metal batteries (LMB), we reduced the lithium salt concentration of the electrolyte (i. e., lithium hexafluorophosphate LiPF 6 ) to a record low 0.1 mol L À 1 LiPF 6 . Herein we present the performance of lithium nickel manganese cobalt oxide (NMC), lithium manganese oxide (LMO), lithium iron phosphate (LFP) cathodes together with graphite and lithium metal anodes in a ternary solvent mixture of ethylene carbonate (EC), ethyl methyl carbonate (EMC), and 1,1,2,2-tetrafluoroethyl 2,2,2trifluoroethyl ether (TFE) (3EC/7EMC/20TFE, by weight) containing 0.1 mol L À 1 LiPF 6 . By virtue of the favored ionic associations between Li + and PF 6À in the presence of the TFE together with EC and EMC, the half and full coin cells revealed a robust performance at room temperature with high specific capacities and coulombic efficiencies (> 98.5 %) over a wide current range (C/2!2C), high capacity retention, modest energy density (180 to 207 Wh kg À 1 depending on the system), extended calendar life (600 h for the Li symmetric cells), and superior operation to cells using commercial carbonate electrolytes (i. e., 1 mol L À 1 LiPF 6 in EC/EMC, 3/7, v/v). The morphological characterization of the electrodes revealed mild structural degradation, homogenous distribution of the electrode and electrolyte-based elements, as well as the formation of decomposition products, especially for the graphite anode. Overall, this study attests to the compatibility of low-concentrated Li salt electrolytes with promising cathode and anode materials for efficient and costeffective battery systems.