Effect of porosity on electrochemical and mechanical properties of composite Li-ion anodes

被引:54
作者
Antartis, Dimitrios [1 ]
Dillon, Shen [2 ]
Chasiotis, Ioannis [1 ]
机构
[1] Univ Illinois, Aerosp Engn, Urbana, IL 61801 USA
[2] Univ Illinois, Mat Sci & Engn, Urbana, IL 61801 USA
关键词
Graphite; tin; PVDF; lithiation; electrochemical cycling; SOLID-STATE AMORPHIZATION; POLY(VINYLIDENE FLUORIDE); GRAPHITE ANODE; CAPACITY FADE; STRESS EVOLUTION; LITHIUM; ELECTRODES; LITHIATION; BATTERIES; SILICON;
D O I
10.1177/0021998314568653
中图分类号
TB33 [复合材料];
学科分类号
摘要
The electrochemical and mechanical performance of composite anodes for Li+ batteries is greatly affected by the matrix porosity. The role of porosity in the retention of the electrochemical capacity and mechanical durability was investigated for composite anodes with polyvinylidene fluoride/acetylene black matrix and graphite or Sn microscale particles. Graphite anodes with porosities between 40% and 50% demonstrated reliable mechanical performance after electrochemical cycling and consistent electrochemical capacity above 45% porosity cycled at C/5 rate. However, graphite anodes with porosities larger than 50% had negligible mechanical strength. The results of the mechanical and electrochemical studies identified an optimum porosity of approximate to 45% at which the graphite anodes had the highest initial elastic modulus and good strength and extensibility, which also agreed with the properties of the polyvinylidene fluoride/acetylene black matrix for the same porosity. The mechanical performance of Sn anodes, however, was quite inferior to that of graphite, which was largely due to the large volumetric expansion of the Sn particles in the first lithiation cycle.
引用
收藏
页码:1849 / 1862
页数:14
相关论文
共 59 条
[1]   Lithium Ion Battery Anode Aging Mechanisms [J].
Agubra, Victor ;
Fergus, Jeffrey .
MATERIALS, 2013, 6 (04) :1310-1325
[2]   Nanostructured materials for advanced energy conversion and storage devices [J].
Aricò, AS ;
Bruce, P ;
Scrosati, B ;
Tarascon, JM ;
Van Schalkwijk, W .
NATURE MATERIALS, 2005, 4 (05) :366-377
[3]   The electrochemical reaction of lithium with tin studied by in situ AFM [J].
Beaulieu, LY ;
Beattie, SD ;
Hatchard, TD ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (04) :A419-A424
[4]   Stress evolution and capacity fade in constrained lithium-ion pouch cells [J].
Cannarella, John ;
Arnold, Craig B. .
JOURNAL OF POWER SOURCES, 2014, 245 :745-751
[5]   Electrochemical behavior of nanocrystalline tin oxide electrodeposited on a Cu substrate for Li-ion batteries [J].
Chang, ST ;
Leu, IC ;
Liao, CL ;
Yen, JH ;
Hon, MH .
JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (12) :1821-1826
[6]  
Chen Q, 2013, NAT MATER, V12, P1102, DOI [10.1038/NMAT3741, 10.1038/nmat3741]
[7]   Study of the mechanical and electrical properties of carbon/poly(vinylidene fluoride-tetrafluoroethylenepropylene) films crosslinked with triethylenetetramine: Possible application as binder for lithium-ion battery electrodes [J].
Chen, ZH ;
Christensen, L ;
Dahn, JR .
JOURNAL OF APPLIED POLYMER SCIENCE, 2004, 91 (05) :2949-2957
[8]   Comparison of PVDF and PVDF-TFE-P as binders for electrode materials showing large volume changes in lithium-ion batteries [J].
Chen, ZH ;
Christensen, L ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (08) :A1073-A1078
[9]   The influence of surface mechanics on diffusion induced stresses within spherical nanoparticles [J].
Cheng, Yang-Tse ;
Verbrugge, Mark W. .
JOURNAL OF APPLIED PHYSICS, 2008, 104 (08)
[10]   Evolution of stress within a spherical insertion electrode particle under potentiostatic and galvanostatic operation [J].
Cheng, Yang-Tse ;
Verbrugge, Mark W. .
JOURNAL OF POWER SOURCES, 2009, 190 (02) :453-460