Silyl-group functionalized organic additive for high voltage Ni-rich cathode material

被引:35
作者
Jang, Seol Heui [1 ,2 ]
Jung, Kwangeun [1 ,2 ]
Yim, Taeeun [1 ,2 ]
机构
[1] Incheon Natl Univ, Dept Chem, 119 Acad Ro, Incheon 406772, South Korea
[2] Incheon Natl Univ, Coll Nat Sci, Res Inst Basic Sci, 119 Acad Ro, Incheon 406772, South Korea
基金
新加坡国家研究基金会;
关键词
Lithium ion battery; Silyl functional group; Electrolyte; Cathode; Additive; LITHIUM ION BATTERIES; ELECTROCHEMICAL PERFORMANCE; LIPF6-BASED ELECTROLYTES; THERMAL-DECOMPOSITION; VINYLENE CARBONATE; GRAPHITE ANODE; LI; SURFACE; SEI; INSTABILITY;
D O I
10.1016/j.cap.2018.07.016
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
To allow stable cycling of layered nickel-rich cathode material at high voltage, silyl-functionalized dimethoxydimethylsilane is proposed as a multi-functional additive. In contrast to typical functional additive, dimethoxydimethylsilane does not make artificial cathode-electrolyte interfaces by electrochemical oxidation because it is quite stable under anodic polarization. We find that dimethoxydimethylsilane mainly focuses on scavenging nucleophilic fluoride species that can be produced by electrolyte decomposition during cycling, leading to improving interfacial stability of both nickel-rich cathode and graphite anode. As a result, the cell cycled with dimethoxydimethylsilane-controlled electrolyte exhibits 65.7% of retention after 100 cycle, which is identified by systematic spectroscopic analyses for the cycled cell.
引用
收藏
页码:1345 / 1351
页数:7
相关论文
共 49 条
[1]   The state of understanding of the lithium-ion-battery graphite solid electrolyte interphase (SEI) and its relationship to formation cycling [J].
An, Seong Jin ;
Li, Jianlin ;
Daniel, Claus ;
Mohanty, Debasish ;
Nagpure, Shrikant ;
Wood, David L., III .
CARBON, 2016, 105 :52-76
[2]   Building better batteries [J].
Armand, M. ;
Tarascon, J. -M. .
NATURE, 2008, 451 (7179) :652-657
[3]   Recent studies on the correlation between surface chemistry, morphology, three-dimensional structures and performance of Li and Li-C intercalation anodes in several important electrolyte systems [J].
Aurbach, D ;
Zaban, A ;
Ein-Eli, Y ;
Weissman, I ;
Chusid, O ;
Markovsky, B ;
Levi, M ;
Levi, E ;
Schechter, A ;
Granot, E .
JOURNAL OF POWER SOURCES, 1997, 68 (01) :91-98
[4]   A study of highly oriented pyrolytic graphite as a model for the graphite anode in Li-ion batteries [J].
Bar-Tow, D ;
Peled, E ;
Burstein, L .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (03) :824-832
[5]   Thermal decomposition of LiPF6-based electrolytes for lithium-ion batteries [J].
Campion, CL ;
Li, WT ;
Lucht, BL .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (12) :A2327-A2334
[6]  
Carey A.Francis, 2006, ADV ORGANIC CHEM A
[7]   The cathode-electrolyte interface in the Li-ion battery [J].
Edström, K ;
Gustafsson, T ;
Thomas, JO .
ELECTROCHIMICA ACTA, 2004, 50 (2-3) :397-403
[8]  
Emsley J. W., 1968, HIGH RESOLUTION NUCL
[9]   A comparative XPS surface study of Li2FeSiO4/C cycled with LiTFSI- and LiPF6-based electrolytes [J].
Ensling, David ;
Stjerndahl, Marten ;
Nyten, Anton ;
Gustafsson, Torbjorn ;
Thomas, John O. .
JOURNAL OF MATERIALS CHEMISTRY, 2009, 19 (01) :82-88
[10]   Effects of vinylene carbonate on high temperature storage of high voltage Li-ion batteries [J].
Eom, Ji-Yong ;
Jung, In-Ho ;
Lee, Jong-Hoon .
JOURNAL OF POWER SOURCES, 2011, 196 (22) :9810-9814