Bismuth-Antimony Alloy Embedded in Carbon Matrix for Ultra-Stable Sodium Storage

被引:5
作者
Ma, Wensheng [1 ]
Yu, Bin [1 ]
Tan, Fuquan [1 ]
Gao, Hui [1 ]
Zhang, Zhonghua [1 ]
机构
[1] Shandong Univ, Sch Mat Sci & Engn, Key Lab Liquid Solid Struct Evolut & Proc Mat, Minist Educ, Jingshi Rd 17923, Jinan 250061, Peoples R China
基金
中国博士后科学基金;
关键词
bismuth-antimony anodes; carbon framework; pyrolysis method; XRD; sodium-ion batteries; ION BATTERIES; SB; ELECTROLYTE; CAPACITY; ANODES; PERFORMANCE; EVOLUTION; SHELL;
D O I
10.3390/ma16062189
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
Alloy-type anodes are the most promising candidates for sodium-ion batteries (SIBs) due to their impressive Na storage capacity and suitable voltage platform. However, the implementation of alloy-type anodes is significantly hindered by their huge volume expansion during the alloying/dealloying processes, which leads to their pulverization and detachment from current collectors for active materials and the unsatisfactory cycling performance. In this work, bimetallic Bi-Sb solid solutions in a porous carbon matrix are synthesized by a pyrolysis method as anode material for SIBs. Adjustable alloy composition, the introduction of porous carbon matrix, and nanosized bimetallic particles effectively suppress the volume change during cycling and accelerate the electrons/ions transport kinetics. The optimized Bi1Sb1@C electrode exhibits an excellent electrochemical performance with an ultralong cycle life (167.2 mAh g(-1) at 1 A g(-1) over 8000 cycles). In situ X-ray diffraction investigation is conducted to reveal the reversible and synchronous sodium storage pathway of the Bi1Sb1@C electrode: (Bi,Sb) (SIC) Na(Bi,Sb) (SIC) Na-3(Bi,Sb). Furthermore, online electrochemical mass spectrometry unveils the evolution of gas products of the Bi1Sb1@C electrode during the cell operation.
引用
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页数:14
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