2005
DOI: 10.1016/j.jpowsour.2005.03.174
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Clarifying the Butler–Volmer equation and related approximations for calculating activation losses in solid oxide fuel cell models

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Cited by 252 publications
(144 citation statements)
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“…This deviation from linearity of activation losses is analogous to that frequently observed at operating temperatures below 900˝C and has been highlighted and discussed on theoretical grounds [29]. Marked bending of I-V curves caused by non-linear activation losses has often been observed experimentally [30].…”
Section: Local Electrochemical Kineticssupporting
confidence: 53%
“…This deviation from linearity of activation losses is analogous to that frequently observed at operating temperatures below 900˝C and has been highlighted and discussed on theoretical grounds [29]. Marked bending of I-V curves caused by non-linear activation losses has often been observed experimentally [30].…”
Section: Local Electrochemical Kineticssupporting
confidence: 53%
“…As a common assumption for fuel cells [19], the charge transfer coefficient α is considered equal to 0.5.…”
Section: Chemical Reaction Modellingmentioning
confidence: 99%
“…Ultimately, the continuity equation of the ionic charge inside the representative volume is obtained by coupling equations (9), (19), (25) and (27) and dividing by V:…”
Section: Equations For Mass and Chargementioning
confidence: 99%
“…in its simplest form (the high-field approximation 10,28 ), relates the current density i and the total double-layer overpotentials η. i 0 is the exchange-current density flowing back and forth across the interface when the cell is in equilibrium, and is proportional to the charge-transfer reaction rate. The applied potential difference V cell is distributed across the three overpotentials of the cell:…”
Section: Electrochemical Reactions In a Driven Soecmentioning
confidence: 99%