Study of Substrate for the Zinc Electrode in Acid Zn-PbO2 Flow Battery

2014 ◽  
Vol 700 ◽  
pp. 136-140
Author(s):  
Han Min Liu ◽  
Jie Cheng ◽  
Yue Hua Wen ◽  
Jun Li Pan ◽  
Gao Ping Cao

An investigation into the suitability of carbon materials, metallic lead and its alloys as substrates for the zinc electrode in acid Zn-PbO2 flow batteries was performed. No maximum current appears on the potentiostatic current transients recorded for the zinc deposition on the lead and its alloys. With increasing the overpotential, the progressive nucleation turns to be the 3D-instantaneous nucleation process employed for the resin-graphite composite. Hydrogen evolution on the graphite composite is effectively suppressed due to the doping of polymer resins. The rate of hydrogen evolution reaction on the lead is relatively weak, but on the lead alloys, the hydrogen evolution conversely becomes serious to a certain degree. Though the exchange current density of the zinc deposition and dissolution process on the graphite composite is relatively low, the zinc corrosion is weakened to a great extent. With the increase of deposition time, the zinc deposits tend to be more compact. Zinc galvanostatic charge-discharge cycling on the graphite composite reveals that the coulombic of over 90% can be found, exhibiting an excellent cycling stability.

2008 ◽  
Vol 59 (5) ◽  
Author(s):  
Viorel Branzoi ◽  
Alina Pruna ◽  
Florina Branzoi

The inhibition of zinc corrosion in 3.5% NaCl solution by some organic compounds (sodium dodecylsulphate (SDS), sodium dodecylbenzosulphonate (SDBS) and sodium 1,4-bis(2-etylhexyl) sulphosuccinate (AOT)) was investigated. The inhibition efficiencies were determined by polarization measurements of the zinc electrode in the solution. Electrochemical impedance spectroscopy (EIS) was also used for electrochemical studies of zinc electrode in this medium. The results showed that the used surfactants inhibit the cathodic reaction of hydrogen evolution and at low anodic overvoltage the corrosion process is under activation control, while at high anodic overvoltage the process is under diffusion control.


ChemInform ◽  
1990 ◽  
Vol 21 (22) ◽  
Author(s):  
G. JUHEL ◽  
B. BEDEN ◽  
C. LAMY ◽  
J. M. LEGER ◽  
R. VIGNAUD

1990 ◽  
Vol 35 (2) ◽  
pp. 479-481 ◽  
Author(s):  
G. Juhel ◽  
B. Beden ◽  
C. Lamy ◽  
J.M. Leger ◽  
R. Vignaud

2021 ◽  
Vol 14 (10) ◽  
pp. 5563-5571
Author(s):  
Yihu Li ◽  
Pengfei Wu ◽  
Wei Zhong ◽  
Chunlin Xie ◽  
Yanling Xie ◽  
...  

The preferential adsorption of cation additives enables the transformation of a zinc nucleation mechanism from instantaneous nucleation to progressive nucleation, which ultimately realizes a stable zinc stripping/plating behavior.


1995 ◽  
Vol 73 (2) ◽  
pp. 44-47 ◽  
Author(s):  
L. Mirkova ◽  
Ch. Tsvetkova ◽  
I. Krastev ◽  
M. Monev ◽  
S. Rashkov

2014 ◽  
Vol 1081 ◽  
pp. 53-57
Author(s):  
Dao Bing Huang ◽  
Yuan Qiang Tu ◽  
Jie Cai ◽  
Guan Wen Feng ◽  
Xing Peng Guo

The electrodeposition of zinc from acidic sulphate bath on steel substrate has been studied. The influence of sodium dodecylbenzenesulfonate (SDBS) as surfactant on the mechanism of the electrodeposition process has been investigated using potentiodynamic and cyclic voltammetry (CV) techniques. From the analysis of CV analysis, it is shown that in the surfactant free bath solution, hydrogen evolution occurs together with the zinc deposition. The presence of SDBS shifts the reduction potential of Zn2+ to more negative values, indicating that SDBS to some extent hinder the Zn electrodeposition.


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