Amide-Functionalized Porous Carbonaceous Anode Materials for Lithium-Ion Batteries

被引:3
作者
Lee, Dong-Geon [1 ,2 ]
Yim, Taeeun [2 ]
Woo, Sang-Gil [1 ]
Yu, Ji-Sang [1 ]
机构
[1] Korea Elect Technol Inst, Adv Batteries Res Ctr, 25 Saenari Ro, Seongnam Si 13509, Gyeonggi Do, South Korea
[2] Incheon Natl Univ, Dept Chem, Res Inst Basic Sci, 119 Acad Ro, Incheon 22012, South Korea
基金
新加坡国家研究基金会;
关键词
amidation; anodes; carbon; lithium-ion batteries; surface modification; MESOCARBON MICROBEADS; MESOPOROUS CARBONS; NEGATIVE ELECTRODE; CAPACITY; PERFORMANCE; MECHANISMS; INSERTION; STORAGE; INTERCALATION; PYROLYSIS;
D O I
10.1002/cphc.201801018
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
Porous carbonaceous anode materials have received considerable attention as an alternative anode material, however, there is a critical bottleneck as it suffers from a large irreversible specific capacity loss over several initial cycles owing to undesired surface reactions. In order to suppress undesired surface reactions of porous carbonaceous anode material, here, we suggest a simple and convenient two-step surface modification approach that allows the embedding of an amide functional group on the surface of a porous carbonaceous anode, which effectively improves the surface stability. In this approach, the porous carbonaceous anode material is firstly activated by means of strong acid treatment comprising a combination of H2SO4 and HNO3, and it is subjected to further modification by means of an amide coupling reaction. Our additional systematic analyses confirm that the acid functional group effectively transforms into the amide functional group. The resulting amide-functionalized porous carbon exhibits an improved electrochemical performance: the initial discharge specific capacity is greatly reduced to less than 2,620 mA h g(-1) and charge specific capacity is well still remained, indicating stabling cycling performance of the cell.
引用
收藏
页码:752 / 756
页数:5
相关论文
共 46 条
[1]   Building better batteries [J].
Armand, M. ;
Tarascon, J. -M. .
NATURE, 2008, 451 (7179) :652-657
[2]   Capacity fade mechanisms and side reactions in lithium-ion batteries [J].
Arora, P ;
White, RE ;
Doyle, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (10) :3647-3667
[3]   A short review of failure mechanisms of lithium metal and lithiated graphite anodes in liquid electrolyte solutions [J].
Aurbach, D ;
Zinigrad, E ;
Cohen, Y ;
Teller, H .
SOLID STATE IONICS, 2002, 148 (3-4) :405-416
[4]   A comparative study of amide -bond forming reagents in aqueous media - Substrate scope and reagent compatibility [J].
Badland, Matthew ;
Crook, Robert ;
Delayre, Bastien ;
Fussell, Steven J. ;
Gladwell, Lain ;
Hawksworth, Michael ;
Howard, Roger M. ;
Walton, Robert ;
Weisenburger, Gerald A. .
TETRAHEDRON LETTERS, 2017, 58 (46) :4391-4394
[5]   Safety mechanisms in lithium-ion batteries [J].
Balakrishnan, PG ;
Ramesh, R ;
Kumar, TP .
JOURNAL OF POWER SOURCES, 2006, 155 (02) :401-414
[6]   RETRACTED: Theoretical Limits of Energy Density in Silicon-Carbon Composite Anode Based Lithium Ion Batteries (Retracted Article) [J].
Dash, Ranjan ;
Pannala, Sreekanth .
SCIENTIFIC REPORTS, 2016, 6
[7]   Electrical Energy Storage for the Grid: A Battery of Choices [J].
Dunn, Bruce ;
Kamath, Haresh ;
Tarascon, Jean-Marie .
SCIENCE, 2011, 334 (6058) :928-935
[8]   A DRIFTS STUDY OF THE FORMATION OF SURFACE GROUPS ON CARBON BY OXIDATION [J].
FANNING, PE ;
VANNICE, MA .
CARBON, 1993, 31 (05) :721-730
[9]   Carbon materials for lithium-ion rechargeable batteries [J].
Flandrois, S ;
Simon, B .
CARBON, 1999, 37 (02) :165-180
[10]   STUDIES OF LITHIUM INTERCALATION INTO CARBONS USING NONAQUEOUS ELECTROCHEMICAL-CELLS [J].
FONG, R ;
VONSACKEN, U ;
DAHN, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (07) :2009-2013