Advanced Proton Conducting Ceramic Cell as Energy Storage Device

被引:24
作者
Marrony, M. [1 ]
Dailly, J. [1 ]
机构
[1] European Inst Energy Res, D-76131 Karlsruhe, Germany
关键词
OXIDE FUEL-CELLS; HIGH-PERFORMANCE; ELECTROLYTE; MEMBRANES; HYDROGEN; STABILITY; OPERATION; CATHODE;
D O I
10.1149/2.1541709jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Ba-based protonic ceramic cell (PCC) was investigated under galvanostatic electrolysis and reversible Fuel cell/electrolysis cycles modes. Such PCC has been made by industrial wet chemical routes (tape casting and screen-printing methods) and by using NiO-BaCe0.8Zr0.1Y0.1O3-delta (BCZY81) as anode/BCZY81-ZnO (5 mol%) as electrolyte, Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF) - BCZY81) as air electrode and BSCF as current collector. The optimization of key parameters of both fuel cell and electrolysis operating conditions such as water feed content, fuel utilization, temperature operation allow to validating promising electrical cell performances (> 0.25 W/cm(2), 0.7 V under fuel cell mode; 0.5 A/cm(2), 1.3 V under electrolysis mode) and reliability during more than 3500 h with limited electrical degradation (< 2%/kh) at 700 degrees C. The evolution of Electrochemical Impedance Spectroscopy measurements reveals that the total electrical resistances of PCC are lower under electrolysis than under fuel cell mode, in particular the ohmic resistance (electrolyte). But in the same time, the polarization resistance of the cell (air electrode interface) is higher under electrolysis mode. The combination of high temperature and water vapor pressure can induce negative reaction able to accelerate the Ba-based materials aging. In any case, it highlights the use of PCC technology as high efficient energy storage candidate. (C) 2017 The Electrochemical Society. All rights reserved.
引用
收藏
页码:F988 / F994
页数:7
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