A new class of Solvent-in-Salt electrolyte for high-energy rechargeable metallic lithium batteries

被引:2362
作者
Suo, Liumin [1 ]
Hu, Yong-Sheng [1 ]
Li, Hong [1 ]
Armand, Michel [1 ]
Chen, Liquan [1 ]
机构
[1] Chinese Acad Sci, Key Lab Renewable Energy, Beijing Key Lab New Energy Mat & Devices, Beijing Natl Lab Condensed Matter Phys,Inst Phys, Beijing 100190, Peoples R China
关键词
RAY PHOTOELECTRON-SPECTROSCOPY; SULFUR BATTERIES; ELECTROCHEMICAL PROPERTIES; LI/S BATTERY; CARBON; ION; CATHODE; TRANSPORT; CONDUCTIVITY; PERFORMANCE;
D O I
10.1038/ncomms2513
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Liquid electrolyte plays a key role in commercial lithium-ion batteries to allow conduction of lithium-ion between cathode and anode. Traditionally, taking into account the ionic conductivity, viscosity and dissolubility of lithium salt, the salt concentration in liquid electrolytes is typically less than 1.2 mol l(-1). Here we show a new class of 'Solvent-in-Salt' electrolyte with ultrahigh salt concentration and high lithium-ion transference number (0.73), in which salt holds a dominant position in the lithium-ion transport system. It remarkably enhances cyclic and safety performance of next-generation high-energy rechargeable lithium batteries via an effective suppression of lithium dendrite growth and shape change in the metallic lithium anode. Moreover, when used in lithium-sulphur battery, the advantage of this electrolyte is further demonstrated that lithium polysulphide dissolution is inhibited, thus overcoming one of today's most challenging technological hurdles, the 'polysulphide shuttle phenomenon'. Consequently, a coulombic efficiency nearing 100% and long cycling stability are achieved.
引用
收藏
页数:9
相关论文
共 60 条
[2]
RUBBERY SOLID ELECTROLYTES WITH DOMINANT CATIONIC TRANSPORT AND HIGH AMBIENT CONDUCTIVITY [J].
ANGELL, CA ;
LIU, C ;
SANCHEZ, E .
NATURE, 1993, 362 (6416) :137-139
[4]
Building better batteries [J].
Armand, M. ;
Tarascon, J. -M. .
NATURE, 2008, 451 (7179) :652-657
[5]
Armand M. B., 1979, Fast Ion Transport in Solids. Electrodes and Electrolytes, P131
[6]
AURBACH D, 1990, ELECTROCHIM ACTA, V35, P625, DOI 10.1016/0013-4686(90)87055-7
[7]
THE CORRELATION BETWEEN SURFACE-CHEMISTRY, SURFACE-MORPHOLOGY, AND CYCLING EFFICIENCY OF LITHIUM ELECTRODES IN A FEW POLAR APROTIC SYSTEMS [J].
AURBACH, D ;
GOFER, Y ;
LANGZAM, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1989, 136 (11) :3198-3205
[8]
The study of electrolyte solutions based on solvents from the ''glyme'' family (linear polyethers) for secondary Li battery systems [J].
Aurbach, D ;
Granot, E .
ELECTROCHIMICA ACTA, 1997, 42 (04) :697-718
[9]
X-ray photoelectron spectroscopy studies of lithium surfaces prepared in several important electrolyte solutions. A comparison with previous studies by Fourier transform infrared spectroscopy [J].
Aurbach, D ;
Weissman, I ;
Schechter, A ;
Cohen, H .
LANGMUIR, 1996, 12 (16) :3991-4007
[10]
On the Surface Chemical Aspects of Very High Energy Density, Rechargeable Li-Sulfur Batteries [J].
Aurbach, Doron ;
Pollak, Elad ;
Elazari, Ran ;
Salitra, Gregory ;
Kelley, C. Scordilis ;
Affinito, John .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2009, 156 (08) :A694-A702