A new family of cation-disordered Zn(Cu)-Si-P compounds as high-performance anodes for next-generation Li-ion batteries

被引:67
作者
Li, Wenwu [1 ,2 ]
Li, Xinwei [3 ]
Liao, Jun [1 ]
Zhao, Bote [2 ]
Zhang, Lei [2 ]
Huang, Le [1 ]
Liu, Guoping [1 ]
Guo, Zaiping [4 ]
Liu, Meilin [2 ]
机构
[1] Guangdong Univ Technol, Sch Mat & Energy, Guangzhou 51006, Guangdong, Peoples R China
[2] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[3] Southern Univ Sci & Technol, Dept Mech & Energy Engn, Shenzhen 518071, Peoples R China
[4] Univ Wollongong, Sch Mech Mat & Mechatron Engn, Inst Superconducting & Elect Mat, North Wollongong, NSW 2500, Australia
基金
中国博士后科学基金; 美国国家科学基金会; 中国国家自然科学基金;
关键词
REDUCED GRAPHENE OXIDE; HIGH-CAPACITY ANODE; SUPERIOR HIGH-RATE; LITHIUM-ION; REVERSIBLE ANODE; PHOSPHORUS; HETEROSTRUCTURES; NANOPARTICLES; NANOSPHERES; ELECTRODES;
D O I
10.1039/c9ee00953a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of low-cost, high-performance anode materials for Li-ion batteries (LIBs) is imperative to meet the ever-increasing demands for advanced power sources. Here we report our findings on the design, synthesis, and characterization of a new cation-disordered ZnSiP2 anode. When tested in LIBs, the disordered phase of ZnSiP2 demonstrates faster reaction kinetics and higher energy efficiency than the cation-ordered phase of ZnSiP2. The superior performance is attributed to the greater electronic and ionic conductivity and better tolerance against volume variation during cycling, as confirmed by theoretical calculations and experimental measurements. Moreover, the cation-disordered ZnSiP2/C composite exhibits excellent cycle stability and superior rate capability. The performance surpasses all reported multi-phase anodes studied. Further, a number of the cation-disordered phases in the Zn(Cu)-Si-P family with a wide range of cation ratios show similar performance, achieving large specific capacities and high first-cycle coulombic efficiency while maintaining desirable working potentials for enhanced safety.
引用
收藏
页码:2286 / 2297
页数:12
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