Chemical Sciences and Engineering, Argonne National Laboratory, Lemont, IL 60439, USA.
Department of Chemistry, University of California, Riverside, Riverside, CA 92521, USA.
Angew Chem Int Ed Engl. 2022 Dec 19;61(51):e202208158. doi: 10.1002/anie.202208158. Epub 2022 Nov 17.
Realization of practical sodium metal batteries (SMBs) is hindered due to lack of compatible electrolyte components, dendrite propagation, and poor understanding of anodic interphasial chemistries. Chemically robust liquid electrolytes that facilitate both favorable sodium metal deposition and a stable solid-electrolyte interphase (SEI) are ideal to enable sodium metal and anode-free cells. Herein we present advanced characterization of a novel fluorine-free electrolyte utilizing the [HCB H ] anion. Symmetrical Na cells operated with this electrolyte exhibit a remarkably low overpotential of 0.032 V at a current density of 2.0 mA cm and a high coulombic efficiency of 99.5 % in half-cell configurations. Surface characterization of electrodes post-operation reveals the absence of dendritic sodium nucleation and a surprisingly stable fluorine-free SEI. Furthermore, weak ion-pairing is identified as key towards the successful development of fluorine-free sodium electrolytes.
实用钠金属电池(SMB)的实现受到缺乏兼容电解质组分、枝晶生长以及对阳极相间化学缺乏深入理解的阻碍。化学稳定的液态电解质有利于促进钠金属的沉积和稳定的固体电解质相间(SEI),是实现钠金属和无阳极电池的理想选择。在此,我们利用[HCB H]阴离子对一种新型无氟电解质进行了先进的表征。使用该电解质的对称 Na 电池在 2.0 mA·cm 的电流密度下表现出极低的过电位 0.032 V,在半电池配置中具有高达 99.5%的库仑效率。电极运行后的表面表征显示出没有枝晶状钠成核,而且出乎意料的是形成了无氟的稳定 SEI。此外,弱离子配对被确定是开发无氟钠电解质的关键。