Ultrafast solid-state lithium ion conductor through alloying induced lattice softening of Li6PS5Cl

被引:66
作者
Xuan, Minjie [1 ,2 ]
Xiao, Weidong [1 ,2 ]
Xu, Hongjie [1 ,2 ]
Shen, Yonglong [1 ,2 ]
Li, Zhenzhen [1 ]
Zhang, Shijie [1 ,2 ]
Wang, Zhuo [1 ,2 ]
Shao, Guosheng [1 ,2 ]
机构
[1] Zhengzhou Univ, State Ctr Int Cooperat Designer Low Carbon & Envi, 100 Kexue Ave, Zhengzhou 450001, Henan, Peoples R China
[2] ZMGI, Bldg 2, Zhengzhou 450100, Henan, Peoples R China
关键词
ELECTROLYTES; BATTERY; PERFORMANCE; TRANSITION; MECHANISMS; DESIGN; TIO2;
D O I
10.1039/c8ta07240j
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
The development of a solid electrolyte with superb Li+ conductivity is the key to enabling safe and high-performance all-solid lithium ion batteries which are free of the safety issues associated with flammable organic liquid electrolyte. Systematic experimental work has been carried out as a follow up to our recent theoretical prediction that superb ionic conductivity could be achieved through the tuning of the lattice chemistry in the cubic argyrodite Li6PS5Cl. Remarkable enhancement of the ionic conductivity has been achieved through the combined effect of excess Li and substitution of S with Te. This leads to an alloy, Li6.25PTe0.125S5.125Cl0.75, having the superb Li+ conductivity of 4.5 mS cm(-1) at 25 degrees C, together with a low activation energy of 0.16 eV to safeguard adequate ionic conductivity at low temperature. This current work conclusively affirms the theoretical outcome that the superb ionic conductivity is attributed to weakened bonding, an enlarged unit cell, and a softened lattice, making it easier for the long-distance diffusion of Li+. In addition, this new class of solid electrolyte based on cubic chalcogenide is electrochemically compatible with the Li anode over a large potential window up to 7 V, which is highly desirable for high performance solid lithium ion batteries.
引用
收藏
页码:19231 / 19240
页数:10
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共 50 条
[1]   Structural requirements for fast lithium ion migration in Li10GeP2S12 [J].
Adams, Stefan ;
Rao, R. Prasada .
JOURNAL OF MATERIALS CHEMISTRY, 2012, 22 (16) :7687-7691
[2]   Displacements, Mean-Squared Displacements, and Codisplacennents for the Calculation of Nonequilibrium Properties [J].
Agnihotri, Mithila V. ;
Chen, Si-Han ;
Beck, Corey ;
Singer, Sherwin J. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2014, 118 (28) :8170-8178
[3]  
[Anonymous], 2012, ENERGY ENV SCI
[4]   Building better batteries [J].
Armand, M. ;
Tarascon, J. -M. .
NATURE, 2008, 451 (7179) :652-657
[5]   Inorganic Solid-State Electrolytes for Lithium Batteries: Mechanisms and Properties Governing Ion Conduction [J].
Bachman, John Christopher ;
Muy, Sokseiha ;
Grimaud, Alexis ;
Chang, Hao-Hsun ;
Pour, Nir ;
Lux, Simon F. ;
Paschos, Odysseas ;
Maglia, Filippo ;
Lupart, Saskia ;
Lamp, Peter ;
Giordano, Livia ;
Shao-Horn, Yang .
CHEMICAL REVIEWS, 2016, 116 (01) :140-162
[6]   PROJECTOR AUGMENTED-WAVE METHOD [J].
BLOCHL, PE .
PHYSICAL REVIEW B, 1994, 50 (24) :17953-17979
[7]   Mechanochemical synthesis of Li-argyrodite Li6PS5X (X = Cl, Br, I) as sulfur-based solid electrolytes for all solid state batteries application [J].
Boulineau, Sylvain ;
Courty, Matthieu ;
Tarascon, Jean-Marie ;
Viallet, Virginie .
SOLID STATE IONICS, 2012, 221 :1-5
[8]   THE ANALYSIS OF ELECTRODE IMPEDANCES COMPLICATED BY THE PRESENCE OF A CONSTANT PHASE ELEMENT [J].
BRUG, GJ ;
VANDENEEDEN, ALG ;
SLUYTERSREHBACH, M ;
SLUYTERS, JH .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 176 (1-2) :275-295
[9]   First-principles modeling of lithium ordering in the LLTO (LixLa2/3-x/3TiO3) superionic conductor [J].
Catti, Michele .
CHEMISTRY OF MATERIALS, 2007, 19 (16) :3963-3972
[10]   Stability and ionic mobility in argyrodite-related lithium-ion solid electrolytes [J].
Chen, Hao Min ;
Chen Maohua ;
Adams, Stefan .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2015, 17 (25) :16494-16506