The secondary lithium—aluminium electrode at room temperature: II. Kinetics of the electrochemical formation of the lithium—aluminium alloy
✍ Scribed by Y. Geronov; P. Zlatilova; G. Staikov
- Book ID
- 103897982
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 505 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0378-7753
No coin nor oath required. For personal study only.
✦ Synopsis
The kinetics of the electrochemical formation of lithium-aluminium alloy was studied by voltammetric, potentiostatic, and pulse galvanostatic techniques in 1M LiCIO4-propylene carbonate solutions.
It was established that the rate of formation of Li-A! alloy up to a thickness of 30/~m is controlled by the dynamics of the interaction between the two metals. The rate constant for this process was found to be a function of the applied potential with values between 10 -6 and 10 -7 cm/s.
A diffusion coefficient of lithium into aluminium equal to 2.4 X 10 -11 cm2/s was also determined from the initial decay of the potentiostatic transients.
Values of the exchange current density (i0), 2.5 mA/cm 2 at 20 °C, and of the apparent activation energy (AH0) , 4.3 kcal/mol, for the process of lithium incorporation into the ~-phase of lithium-aluminium were found from micropolarization measurements.
📜 SIMILAR VOLUMES
Abstrafl--Hydrogen evolution and aluminium electrodissolution processes were investigated by cu and wulometric methods on Al electrode at the cathodic end of the polarization curve. The proton or water is reduced at the passive layer with a diffusion controlled rate. The water wntent of the passive