Active parts for CH4 decomposition and electrochemical oxidation at metal/oxide interfaces by isotope labeling-secondary ion mass spectrometry

被引:12
作者
Horita, Teruhisa
Kishimoto, Haruo
Yamaji, Katsuhiko
Sakai, Natsuko
Xiong, Yueping
Brito, Manuel E.
Yokokawa, Harumi
Rai, Muneaki
Amezawa, Koji
Uchimoto, Yoshiharu
机构
[1] Natl Inst AIST, Tsukuba, Ibaraki 3058565, Japan
[2] Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
关键词
solid oxide fuel cells (SOFCs); anode/electrolyte interfaces; isotope labeling; secondary ion mass spectrometry (SIMS); XANES/EXAFS;
D O I
10.1016/j.ssi.2006.07.051
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
Active parts for CH4 decomposition and electrochemical oxidation of reformed gases were investigated at the well defined Ni-mesh/oxide interfaces in mu m level. The effective reaction areas were determined by isotope labeling technique under the mixture of CH4, D2O, and O-18(2) at 1073 K. A deposition of carbon preferentially occurred on the Ni-mesh surface on Y2O3-stabilized ZrO2 (YSZ) and SM2O3-doped CeO2 (SDC) electrolyte oxides. A slight reduction of carbon deposition was observed on SDC substrate under non-polarized condition. The electronic and structural properties changes of Ni were observed by XANES/EXAFS analysis. By anodic polarization, a significant reduction of deposited carbon was observed on Ni-mesh surface in Ni-mesh/YSZ and Ni-mesh/SDC samples. Oxygen spill over can be effective for eliminating the deposited carbon on the Ni-mesh. Hydrogen and isotope oxygen concentration (O-18(2)) on the Ni-mesh was changed by the oxide substrates under anodic polarization. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:3179 / 3185
页数:7
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