Improving rate capability and reducing over-potential of lithium-oxygen batteries through optimization of Dimethylsulfoxide-N/N-dimethylacetamide mixed electrolyte

被引:8
作者
Chen, Chunguang [1 ]
Li, Liangyu [1 ]
Su, Junming [1 ]
Zhang, Congcong [1 ]
Chen, Xiang [1 ]
Huang, Tao [1 ]
Yu, Aishui [1 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Shanghai Key Lab Mol Catalysis & Innovat Mat, Dept Chem,Inst New Energy, Shanghai 200438, Peoples R China
关键词
DMSO-based electrolyte; Lithium-oxygen batteries; Mixed electrolyte; N; N-dimethylacetamide; Over-potential; Rate capability; NONAQUEOUS LI-O-2 BATTERIES; AIR BATTERY; CATHODE; PERFORMANCE; STABILITY; SOLVENTS; REDUCTION; RECHARGEABILITY; LIMITATIONS; SOLUBILITY;
D O I
10.1016/j.electacta.2017.05.074
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Although dimethylsulfoxide (DMSO) solvent has been widely researched in rechargeable lithium-oxygen (Li-O-2) batteries, high polarization voltage and low rate capability limited its application. In this work, we reported a DMSO-based electrolyte system by adding N, N-dimethylacetamide (DMA) to adjust its physical and electrochemical properties. The ionic conductivity, viscosity, oxygen solubility and diffusion coefficient of the mixed electrolytes as well as their electrochemical performance in Li-O-2 batteries are researched. The electrochemical tests show that the optimized DMSO/DMA volume ratio is 30 to 70 based on the rate performance and polarization voltage of the cell. Compared with that of the pure DMSO-based electrolyte, the cell with the mixed electrolyte shows improved rate capability and reduced charge-discharge over-potential. When increasing current density from 0.2 to 0.5 mA cm(-2), the capability retention improves from 32% to 59%. Meanwhile, the charge-discharge voltage gap drops from 1.4V to 0.9V at a current density of 0.2 mA cm(-2). The improved electrochemical performance could be attributed to low viscosity, high oxygen solubility and diffusion coefficient as well as the low charge-transfer resistance with the mixed electrolyte. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:357 / 363
页数:7
相关论文
共 46 条
[1]   Electrolyte-Directed Reactions of the Oxygen Electrode in Lithium-Air Batteries [J].
Abraham, K. M. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2015, 162 (02) :A3021-A3031
[2]   A polymer electrolyte-based rechargeable lithium/oxygen battery [J].
Abraham, KM ;
Jiang, Z .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (01) :1-5
[3]   Towards a Stable Organic Electrolyte for the Lithium Oxygen Battery [J].
Adams, Brian D. ;
Black, Robert ;
Williams, Zack ;
Fernandes, Russel ;
Cuisinier, Marine ;
Berg, Erik Jaemstorp ;
Novak, Petr ;
Murphy, Graham K. ;
Nazar, Linda F. .
ADVANCED ENERGY MATERIALS, 2015, 5 (01)
[4]   Current density dependence of peroxide formation in the Li-O2 battery and its effect on charge [J].
Adams, Brian D. ;
Radtke, Claudio ;
Black, Robert ;
Trudeau, Michel L. ;
Zaghib, Karim ;
Nazar, Linda F. .
ENERGY & ENVIRONMENTAL SCIENCE, 2013, 6 (06) :1772-1778
[5]   A critical review on lithium-air battery electrolytes [J].
Balaish, Moran ;
Kraytsberg, Alexander ;
Ein-Eli, Yair .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2014, 16 (07) :2801-2822
[6]   THE SOLUBILITY OF OXYGEN AND OZONE IN LIQUIDS [J].
BATTINO, R ;
RETTICH, TR ;
TOMINAGA, T .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1983, 12 (02) :163-178
[7]  
Battino R., 1981, Solubility Data Series: Oxygen and Ozone, V7
[8]  
Bruce PG, 2012, NAT MATER, V11, P19, DOI [10.1038/nmat3191, 10.1038/NMAT3191]
[9]   Predicting Autoxidation Stability of Ether- and Amide-Based Electrolyte Solvents for Li-Air Batteries [J].
Bryantsev, Vyacheslav S. ;
Faglioni, Francesco .
JOURNAL OF PHYSICAL CHEMISTRY A, 2012, 116 (26) :7128-7138
[10]   Enhancing electrochemical intermediate solvation through electrolyte anion selection to increase nonaqueous Li-O2 battery capacity [J].
Burke, Colin M. ;
Pande, Vikram ;
Khetan, Abhishek ;
Viswanathan, Venkatasubramanian ;
McCloskey, Bryan D. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (30) :9293-9298