Long cycle life of sodium-ion pouch cell achieved by using multiple electrolyte additives

被引:79
作者
Che, Haiying [1 ]
Yang, Xinrong [1 ]
Wang, Hong [1 ]
Liao, Xiao-Zhen [1 ]
Zhang, Sheng S. [2 ]
Wang, Chunsheng [3 ]
Ma, Zi-Feng [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Chem & Chem Engn, Shanghai Electrochem Energy Devices Res Ctr, Shanghai 200240, Peoples R China
[2] US Army Res Lab, Electrochem Branch, Power & Energy Div, Sensor & Electron Devices Directorate, Adelphi, MD 20783 USA
[3] Univ Maryland, Dept Chem & Biomol Engn, College Pk, MD 20740 USA
关键词
Sodium-ion battery; Pouch cell; Electrolyte additive; Hard carbon; Na(x)Hi(1/3)Fe(1/3)Mn(1/3)O(2); HIGH-VOLTAGE CATHODE; NA-ION; ELECTROCHEMICAL PROPERTIES; BATTERIES; INTERPHASE; PERFORMANCE; XPS; FLUOROPHOSPHATE; CHALLENGES; CARBONATE;
D O I
10.1016/j.jpowsour.2018.08.025
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Sodium-ion pouch cells with up to 1000 cycles are presented by using a NaNi1/3Fe1/3Mn1/3O2 cathode, a hard carbon anode, and a functional electrolyte. The functional electrolyte is composed of 1 M NaPF6 dissolved in a 1:1 (v/v) mixed solvent of propylene carbonate (PC) and ethyl methyl carbonate (EMC) with 3-4 wt% of two or three additives, including fluoroethylene carbonate (FEC), prop-1-ene-1,3-sultone (PST), and 1,3,2-Dioxathiolane-2,2-dioxide (DTD). It is shown that the capacity retentions of the cells increase to 84.4% and 92.2% after 1000 cycles for electrolytes containing FEC-PST bi-additive and FEC-PST-DTD tri-additive, respectively, as compared with that containing FEC single additive. Using X-ray photoelectron spectroscopy, inductively coupled plasma optical, and transmission electron microscopy, post-mortem analyses on the surface of the cycled electrodes indicate that PST and DTD are beneficial to the anode by forming an organic compound rich solid electrolyte interphase (SEI), and to the cathode by forming a dense and thick cathode electrolyte interphase (CEI) that consequently prevents transition metal ions from dissolving into electrolyte.
引用
收藏
页码:173 / 179
页数:7
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