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通过阴离子/阳离子溶剂化工程实现的用于4.7 V钠金属电池的高抗氧化电解质。

Highly Oxidation-Resistant Electrolyte for 4.7 V Sodium Metal Batteries Enabled by Anion/Cation Solvation Engineering.

作者信息

Wu Daxiong, Zhu Chunlei, Wu Mingguang, Wang Huaping, Huang Junda, Tang Dongliang, Ma Jianmin

机构信息

School of Physics and Electronics, Hunan University, Changsha, 410082, China.

出版信息

Angew Chem Int Ed Engl. 2022 Dec 23;61(52):e202214198. doi: 10.1002/anie.202214198. Epub 2022 Nov 28.

Abstract

Sodium metal batteries (SMBs) are considered as promising battery system due to abundant Na sources. However, poor compatibility between electrolyte and cathode severely impedes its development. Herein, we proposed an anion/cation solvation strategy for realizing 4.7 V resistant SMBs electrolyte with NaClO and trimethoxy(pentafluorophenyl)silane (TPFS) as dual additives (DA). The ClO can rapidly transfer to the cathode surface and strongly coordinate with Na to form stable polymer-like chains with solvents. Meanwhile, TPFS can preferentially enter into the PF anion solvation sheath for reducing PF -solvent interaction and effectively scavenge adverse electrolyte species for protecting electrode electrolyte interphases. Thus, such electrolyte elevates the oxidative stability of carbonate electrolytes from 3.77 to 4.75 V, and enables Na||Na V (PO ) O F (NVPF) battery with a capacity retention of 93 % and an average Coulombic efficiency (CE) of 99.6 % after 500 cycles at 4.7 V.

摘要

由于钠资源丰富,钠金属电池(SMBs)被认为是一种很有前景的电池系统。然而,电解质与阴极之间的兼容性差严重阻碍了其发展。在此,我们提出了一种阴离子/阳离子溶剂化策略,以实现以高氯酸钠(NaClO)和三甲氧基(五氟苯基)硅烷(TPFS)作为双添加剂(DA)的耐4.7V钠金属电池电解质。ClO 可以迅速转移到阴极表面,并与Na强烈配位,与溶剂形成稳定的聚合物状链。同时,TPFS可以优先进入PF 阴离子溶剂化鞘层,以减少PF -溶剂相互作用,并有效清除有害的电解质物种,从而保护电极电解质界面。因此,这种电解质将碳酸盐电解质的氧化稳定性从3.77V提高到4.75V,并使Na||Na V (PO ) O F(NVPF)电池在4.7V下循环500次后容量保持率达到93%,平均库仑效率(CE)达到99.6%。

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