Rational Design of the Li<sup>+</sup>-Solvation Structure Contributes to Constructing a Robust Cathode-Electrolyte Interphase for a 5 V High-Voltage LiNi<sub>0.5</sub>Mn<sub>1.5</sub>O<sub>4</sub> Cathode
Dichang Guan, Jingyao Zeng, Zhiyuan Xue, Yanbing Cao, Guorong Hu, Zhongdong Peng, Ke Du
Abstract
Spinel oxide LiNi 0.5 Mn 1.5 O 4 (LNMO) presents great potential for lithium-ion batteries (LIBs) due to its high working potential (∼4.7 V vs Li/Li + ) and low cost. Nevertheless, the lack of a competent electrolyte restricts its application. We develop a battery of LiPF 6 -based localized high-concentration electrolytes containing dimethyl carbonate (DMC) and 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (TTE). As the volume ratio of TTE to DMC augments, the percentage of free DMC and PF 6 – and the solvation number of Li + reduce. The proper Li + -solvation structure contributes to forming a robust PF 6 – -derived LiF enriched cathode-electrolyte interphase (CEI). The Li||LNMO cell in the 1M LiPF 6 -DMC/TTE (1:2, V/V) (1M-DT12) electrolyte exhibits wonderful cycling stability (97.5%, after 100 cycles at 1C), superior rate capability (124.0 mA h/g at 5C), and significantly enhanced low-temperature performance (83.1 mA h/g, 0.1C at −30 °C). This work illustrates the rational design of the Li + -solvation structure in the LiPF 6 -based electrolyte to obtain robust PF 6 – -derived LiF enriched CEI for a high-voltage LNMO cathode.