Direct-current-induced transformation at the interface between platinum anode and holmium-doped ceria electrolyte

被引:3
作者
Ou, Ding Rong [1 ]
Mori, Toshiyuki [1 ]
Ye, Fei [1 ]
Zou, Jin [2 ,3 ]
Drennan, John [3 ]
机构
[1] Natl Inst Mat Sci, Fuel Cell Mat Ctr, Tsukuba, Ibaraki 3050044, Japan
[2] Univ Queensland, Sch Engn, St Lucia, Qld 4072, Australia
[3] Univ Queensland, Ctr Microscopy & Microanal, St Lucia, Qld 4072, Australia
基金
日本学术振兴会; 澳大利亚研究理事会;
关键词
ENERGY-LOSS SPECTROSCOPY; X-RAY-ABSORPTION; ELECTRIC-FIELD; PHASE-TRANSITION; CEO2; VALENCE; OXIDE; MICROSTRUCTURES; ZIRCONIA; CATIONS;
D O I
10.1063/1.3142263
中图分类号
O59 [应用物理学];
学科分类号
摘要
Under the influence of a direct current (dc), phase transformation could take place at the interface between platinum anode and holmium-doped ceria (HDC) electrolyte attemperature >= 600 degrees C. This transformation is insensitive to the doping concentration and the sintering temperature, but strongly depends on the testing temperature. As a result of the dc-induced transformation, products with a size up to hundreds of microns were separated from the anode-side surface and, correspondingly, circular holes with diameters varied from tens to hundreds of microns remained on the surface. Compared with original HDC samples, a high degree of local ordering of oxygen vacancies was found in most of the products. Based on structural and compositional studies, it is suggested that the dc-induced transformation could be attributed to the electrochemical reaction at the anode/electrolyte interface and the mobility of Ho cations promoted by the current. c 2009 American Institute of Physics. [DOI: 10.1063/1.3142263]
引用
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页数:5
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