Potassium Salts as Electrolyte Additives in Lithium-Oxygen Batteries

被引:24
作者
Landa-Medrano, Imanol [1 ,2 ]
Olivares-Marin, Mara [2 ,6 ]
Bergner, Benjamin [3 ,7 ]
Pinedo, Ricardo [3 ]
Sorrentino, Andrea [4 ]
Pereiro, Eva [4 ]
Ruiz de Larramendi, Idoia [1 ]
Janek, Jurgen [3 ]
Rojo, Teofilo [1 ,5 ]
Tonti, Dino [2 ]
机构
[1] Univ Pais Vasco UPV EHU, Fac Ciencia & Tecnol, Dept Quim Inorgan, Barrio Sarriena S-N, Leioa 48940, Bizkaia, Spain
[2] CSIC, ICMAB, Inst Ciencia Mat Barcelona, Campus UAB, Barcelona, Spain
[3] Justus Liebig Univ Giessen, Phys Chem Inst, Heinrich Buff Ring 58, D-35392 Giessen, Germany
[4] ALBA Synchrotron Light Source, MISTRAL Beamline Expt Div, Barcelona 08290, Spain
[5] CIC EnergiGUNE, Albert Einstein 48, Minano 0150, Spain
[6] Univ Extremadura, Ctr Univ Merida, Avda Santa Teresa Jornet 38, Merida, Spain
[7] Univ Oxford, Dept Mat, Parks Rd, Oxford OX1 3PH, England
关键词
LI-AIR BATTERIES; NONAQUEOUS LI-O-2 BATTERIES; X-RAY MICROSCOPY; REDOX MEDIATOR; REDUCTION REACTION; CARBON CATHODES; GROWTH; ELECTROCHEMISTRY; MECHANISM; PERFORMANCE;
D O I
10.1021/acs.jpcc.7b00355
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
The stabilization of the intermediates formed during oxygen reduction reaction and their efficient solubilization and diffusion is a crucial issue that needs to be improved in nonaqueous lithium oxygen batteries. By adding 0.1 M K+(as KOTf salt) to the electrolyte, we have observed remarkable improvements in the rate capability of the discharge process. The K+ cation facilitates a more homogeneous discharge product deposition in the porous cathode. Instead, as evidenced by synchrotron measurements, we find that K+ does not influence the cell chemistry, suggesting that it rather assists the superoxide solvation, thus enhancing the solution-based growth of the discharge products. In addition, if iodide (I-) is added as redox mediator, we find an extended cycle life when K+ instead of Li+ is used as cation. This finding remarks the benefits of stabilizing the oxygen reduction products in the electrolyte leading to a solution-based mechanism.
引用
收藏
页码:3822 / 3829
页数:8
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]   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
[3]  
Aetukuri NB, 2015, NAT CHEM, V7, P50, DOI [10.1038/NCHEM.2132, 10.1038/nchem.2132]
[4]   Mass-transport Control on the Discharge Mechanism in Li-O2 Batteries Using Carbon Cathodes with Varied Porosity [J].
Aklalouch, Mohamed ;
Olivares-Marin, Mara ;
Lee, Rung-Chuan ;
Palomino, Pablo ;
Enciso, Eduardo ;
Tonti, Dino .
CHEMSUSCHEM, 2015, 8 (20) :3465-3471
[5]   Identifying Capacity Limitations in the Li/Oxygen Battery Using Experiments and Modeling [J].
Albertus, Paul ;
Girishkumar, G. ;
McCloskey, Bryan ;
Sanchez-Carrera, Roel S. ;
Kozinsky, Boris ;
Christensen, Jake ;
Luntz, A. C. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2011, 158 (03) :A343-A351
[6]  
[Anonymous], 2016, CRC handb. Chem. Phys., DOI DOI 10.1201/9781315380476
[7]   On the Thermodynamics, the Role of the Carbon Cathode, and the Cycle Life of the Sodium Superoxide (NaO2) Battery [J].
Bender, Conrad L. ;
Hartmann, Pascal ;
Vracar, Milos ;
Adelhelm, Philipp ;
Janek, Juergen .
ADVANCED ENERGY MATERIALS, 2014, 4 (12)
[8]   How To Improve Capacity and Cycling Stability for Next Generation Li-O2 Batteries: Approach with a Solid Electrolyte and Elevated Redox Mediator Concentrations [J].
Bergner, Benjamin J. ;
Busche, Marlin R. ;
Pinedo, Ricardo ;
Berkes, Balazs B. ;
Schroeder, Daniel ;
Janek, Juergen .
ACS APPLIED MATERIALS & INTERFACES, 2016, 8 (12) :7756-7765
[9]   TEMPO: A Mobile Catalyst for Rechargeable Li-O2 Batteries [J].
Bergner, Benjamin J. ;
Schuermann, Adrian ;
Peppler, Klaus ;
Garsuch, Arnd ;
Janek, Juergen .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (42) :15054-15064
[10]  
Chen YH, 2013, NAT CHEM, V5, P489, DOI [10.1038/NCHEM.1646, 10.1038/nchem.1646]