“…In the 1980s, ethers were widely preferred by researchers as an alternative candidate, because of their low viscosity and resultant high ionic conductivity, but, most of all, the better lithium morphology during cycling. 60 The cycling efficiency of lithium was reported to be 88% in tetrahydrofuran (THF), [60][61][62] an average of 96% in 2-methyltetrahydrofuran (2-Me-THF), [62][63][64][65] 97% in polymethoxy ethers 66 and dimethoxy propane, 67 and 98% in diethyl ether, 62,68 although the safety concern over the high vapor pressure of diethyl ether renders it an impractical candidate. The formation of dendritic lithium seemed to be sufficiently suppressed in these solvents even at high charge rates.…”