Understanding Direct Borohydride - Hydrogen Peroxide Fuel Cell Performance with a Calibrated Numerical Model

被引:0
|
作者
Stroman, Richard O. [1 ]
Jackson, Gregory S. [2 ]
机构
[1] US Navy, Div Chem, Res Lab, Washington, DC 20375 USA
[2] Colorado Sch Mines, Dept Mech Engn, Golden, CO 80401 USA
来源
POLYMER ELECTROLYTE FUEL CELLS 14 | 2014年 / 64卷 / 03期
关键词
DECOMPOSITION; OXIDATION; KINETICS; AU(111); H2O2; ACID;
D O I
10.1149/06403.0989ecst
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A numerical model is developed for a hydrogen peroxide -direct borohydride fuel cell (H2O2-DBFC) to provide insight into cell processes which are obscured in experiments by the complexity of electrode reactions and transport in the reactant flow channels. In the model, transport is modeled using a 2D finite volume approach. Multi-step electrode reactions, including competing parasitic reactions, are represented by global rate expressions, with parameters calibrated to single-cell experiments. The results are calibrated to a H2O2-DBFC in which fuel (1-50 mM NaBH4/2 M NaOH) is oxidized at a Au anode and oxidizer (10-40 mM H2O2/1 M H2SO4) is reduced at a Pd: Ir cathode. This modeling approach provides critical insight into the rate-limiting processes at different operating conditions of a H2O2-DBFC.
引用
收藏
页码:989 / 998
页数:10
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