Understanding the discharge behavior of an ultra-high-purity Mg anode for Mg-air primary battery

Author(s):  
Xingrui Chen ◽  
Yonghui Jia ◽  
Zhiming Shi ◽  
Qichi Le ◽  
Jingren Li ◽  
...  

This work used both experiments and modeling methods to understand some critical issues of Mg discharge behavior for Mg-air primary batteries. The charge transfer resistance is the main internal anodic...

Energies ◽  
2021 ◽  
Vol 14 (22) ◽  
pp. 7467
Author(s):  
Xuan Zhou ◽  
Ping Li ◽  
Zhihao Tang ◽  
Jialu Liu ◽  
Shaowei Zhang ◽  
...  

The solid electrolyte interphase (SEI) film plays a significant role in the capacity and storage performance of lithium primary batteries. The electrolyte additives are essential in controlling the morphology, composition and structure of the SEI film. Herein, fluoroethylene carbonate (FEC) is chosen as the additive, its effects on the lithium primary battery performance are investigated, and the relevant formation mechanism of SEI film is analyzed. By comparing the electrochemical performance of the Li/AlF3 primary batteries and the microstructure of the Li anode surface under different conditions, the evolution model of the SEI film is established. The FEC additive can decrease the electrolyte decomposition and protect the lithium metal anode effectively. When an optimal 5% FEC is added, the discharge specific capacity of the Li/AlF3 primary battery is 212.8 mAh g−1, and the discharge specific capacities are respectively 205.7 and 122.3 mAh g−1 after storage for 7 days at room temperature and 55 °C. Compared to primary electrolytes, the charge transfer resistance of the Li/AlF3 batteries with FEC additive decreases, indicating that FEC is a promising electrolyte additive to effectively improve the SEI film, increase discharge-specific capacities and promote charge transfer of the lithium primary batteries.


2016 ◽  
Vol 7 ◽  
pp. 1960-1970 ◽  
Author(s):  
Konstantin A Kurilenko ◽  
Oleg A Shlyakhtin ◽  
Oleg A Brylev ◽  
Dmitry I Petukhov ◽  
Alexey V Garshev

Nanocomposites of Li1.4Ni0.5Mn0.5O2+ x and amorphous carbon were obtained by the pyrolysis of linear and cross-linked poly(vinyl alcohol) (PVA) in presence of Li1.4Ni0.5Mn0.5O2+ x . In the case of linear PVA, the formation of nanostructured carbon coatings on Li1.4Ni0.5Mn0.5O2+ x particles is observed, while for cross-linked PVA islands of mesoporous carbon are located on the boundaries of Li1.4Ni0.5Mn0.5O2+ x particles. The presence of the carbon framework leads to a decrease of the polarization upon cycling and of the charge transfer resistance and to an increase in the apparent Li+ diffusion coefficient from 10−16 cm2·s−1 (pure Li1.4Ni0.5Mn0.5O2+ x ) to 10−13 cm2·s−1. The nanosized carbon coatings also reduce the deep electrochemical degradation of Li1.4Ni0.5Mn0.5O2+ x during electrochemical cycling. The nanocomposite obtained by the pyrolysis of linear PVA demonstrates higher values of the apparent lithium diffusion coefficient, a higher specific capacity and lower values of charge transfer resistance, which can be related to the more uniform carbon coatings and to the significant content of sp2-hybridized carbon detected by XPS and by Raman spectroscopy.


2016 ◽  
Vol 219 ◽  
pp. 588-591 ◽  
Author(s):  
Maria A. Komkova ◽  
Elena V. Karpova ◽  
Grigory A. Sukhorukov ◽  
Alexey A. Sadovnikov ◽  
Arkady A. Karyakin

2018 ◽  
Vol 165 (3) ◽  
pp. A493-A500 ◽  
Author(s):  
Prerna Joshi ◽  
Katsuhito Iwai ◽  
Sai Gourang Patnaik ◽  
Raman Vedarajan ◽  
Noriyoshi Matsumi

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