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
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