电解
阳极
聚合物电解质膜电解
材料科学
电解质
介电谱
高温电解
电极
陶瓷
储能
电解槽
极化(电化学)
欧姆接触
电化学
化学工程
化学
复合材料
图层(电子)
功率(物理)
物理化学
工程类
物理
量子力学
作者
Mathieu Marrony,Julian Dailly
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-δ (BCZY81) as anode/BCZY81–ZnO (5 mol%) as electrolyte, Ba0.5Sr0.5Co0.8Fe0.2O3-δ (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/cm², 0.7 V under fuel cell mode; 0.5 A/cm², 1.3 V under electrolysis mode) and reliability during more than 3500 h with limited electrical degradation (<2%/kh) at 700°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.
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