Degradation of solid oxide cells during co-electrolysis of steam and carbon dioxide at high current densities

被引:97
作者
Tao, Youkun [1 ]
Ebbesen, Sune Dalgaard [1 ]
Mogensen, Mogens Bjerg [1 ]
机构
[1] Tech Univ Denmark, Dept Energy Convers & Storage, DTU Riso Campus,Frederiksborgvej 399, DK-4000 Roskilde, Denmark
关键词
Solid oxide electrolysis cells; Energy conversion; Carbon dioxide; Steam; Degradation; ANODE-SUPPORTED SOFCS; FUEL-CELLS; TEMPERATURE; IMPEDANCE; ZIRCONIA; ELECTRODES; H2O; MICROSTRUCTURE; QUANTIFICATION; POLARIZATION;
D O I
10.1016/j.jpowsour.2016.08.055
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
In this work, the durability of Ni-YSZ based solid oxide cells was investigated during co-electrolysis of steam and carbon dioxide (45% H2O + 45% CO2 + 10% H-2) at current density of -1.5 or -2.0 A cm(2). The cell consists of similar to 300 mu m Ni-YSZ support, similar to 10 mu m Ni-YSZ electrode, similar to 10 mu m YSZ electrolyte and similar to 15 mu m LSM-YSZ oxygen electrode. The gas conversion was 45% at -1.5 A cm(-2) and 60% at -2.0 A cm(-2), and the operating durations were up to 700 h. The detailed electrochemical analysis revealed significant increase of the ohmic resistance, oxide ion transport resistance in the Ni-YSZ composite electrodes and the electrochemical reaction resistance at the Ni-YSZ triple-phase boundaries. The performance degradation is mainly ascribed to the microstructural change in the Ni-YSZ electrode close to the YSZ electrolyte, including the percolation loss of Ni, the contact loss between Ni and YSZ electrolyte and the decomposition of YSZ close to Ni-YSZ vertical bar YSZ interface. The electrochemical performance and the microstructure of the oxygen electrode were found to be relatively stable. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:452 / 462
页数:11
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