23,000 h steam electrolysis with an electrolyte supported solid oxide cell

被引:106
|
作者
Schefold, Josef [1 ]
Brisse, Annabelle [1 ]
Poepke, Hendrik [2 ]
机构
[1] European Inst Energy Res EIFER, Emmy Noether Str 11, D-76131 Karlsruhe, Germany
[2] Kerafol Keram Folien GmbH, Koppe Pl 1, D-92676 Eschenbach, Germany
关键词
Solid oxide electrolysis cell; Steam electrolysis; Long-term degradation; Air electrode pollution; Cell reversibility; Impedance; HIGH-TEMPERATURE ELECTROLYSIS; SCANDIA-STABILIZED ZIRCONIA; HIGH-CURRENT DENSITIES; FUEL-CELL; HYDROGEN-PRODUCTION; WATER ELECTROLYSIS; ALKALINE ELECTROLYSIS; CO-ELECTROLYSIS; CURRENT-VOLTAGE; SHORT STACK;
D O I
10.1016/j.ijhydene.2017.01.072
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An electrolyte supported solid oxide cell of 45 cm(2) area was operated in the steam electrolysis mode during more than 23,000 h before scheduled shutdown, of which 20,000 h with a current density of j = -0.9 A cm(-2). The cell consisted of a scandia/ceria doped zirconia electrolyte (6Sc1CeSZ), CGO diffusion-barrier/adhesion layers between electrolyte and electrodes, a lanthanum strontium cobaltite ferrite (LSCF) oxygen electrode, and a nickel/gadolinia-doped ceria (Ni/GDC) steam/hydrogen electrode. Voltage degradation in the operation period with j = -0.9 A cm(-2) was 7.4 mV/1000 h (0.57%/1000 h) and the increase in the area specific resistance 8 m Omega cm(2)/1000 h. The final cell voltage was 1.33 V (at 851 degrees C cell temperature). After dismantling, the cell showed no mechanical damage at electrolyte and H-2/H2O electrode; a small fraction of the oxygen electrode was delaminated. Impedance spectroscopy applied at the steady state DC current density confirmed a degradation dominated by an increasing ohmic term, mainly due to ionic conductivity decay in the electrolyte. In addition, a small non-ohmic and at least partly reversible 02 electrode contribution to degradation was identified, affected by a pollution from the (compressor) purge air. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13415 / 13426
页数:12
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