scholarly journals Evaluation of Exchange Current Density for LSM Porous Cathode Based on Measurement of Three-Phase Boundary Length

2015 ◽  
Vol 68 (1) ◽  
pp. 657-664 ◽  
Author(s):  
K. Miyoshi ◽  
T. Miyamae ◽  
H. Iwai ◽  
M. Saito ◽  
M. Kishimoto ◽  
...  
2008 ◽  
Vol 178 (1) ◽  
pp. 368-372 ◽  
Author(s):  
Vinod M. Janardhanan ◽  
Vincent Heuveline ◽  
Olaf Deutschmann

1996 ◽  
Vol 453 ◽  
Author(s):  
R. M. Williams ◽  
M. A. Ryan ◽  
C. Saipetch ◽  
H. G. LeDuc

AbstractThe exchange current observed at porous metal electrodes on sodium or potassium beta"-alumina solid electrolytes in alkali metal vapor is quantitatively modeled with a multi-step process with good agreement with experimental results. No empirically adjusted parameters were used, although some physical parameters have poor precision. Steps include: (1) diffusion of Na+ ions to the reaction site; (2) stretching of the Na+ ionic bond with the β3"-alumina surface to reach a configuration suitable for accepting an electron to form a surface bound Na0 atom; (3) electron tunneling from the Mo electrode to the ions; and (4) desorption of Na0 atoms weakly bound at the reaction site on the β"-alumina surface; (5) electron tunneling between Na0 or Na+ on the defect block and (6) Na0 and/or Na+ mobility on the spinel block surface may extend the reaction area substantially.The rate is increasingly dominated by the region close to the three-phase boundary as temperature increases and the rate near the three-phase boundary increases fastest, because desorption has a higher energy than reorganization. At high temperatures, surface diffusion of Na+ ions from the defect block edges to the spinel block edges is responsible for an increase in the total effective reaction zone area near the three-phase boundary.


2022 ◽  
Vol 354 ◽  
pp. 131219
Author(s):  
Siyuan Lv ◽  
Yueying Zhang ◽  
Li Jiang ◽  
Lianjing Zhao ◽  
Jing Wang ◽  
...  

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