Performance and methane production characteristics of H2O-CO2 co-electrolysis in solid oxide electrolysis cells

被引:118
|
作者
Li, Wenying [1 ]
Wang, Hongjian [1 ]
Shi, Yixiang [1 ]
Cai, Ningsheng [1 ]
机构
[1] Tsinghua Univ, Key Lab Thermal Sci & Power Engn, Minist Educ, Beijing 100084, Peoples R China
关键词
Solid oxide electrolysis cell; H2O-CO2; co-electrolysis; Electrochemical performance; Methane; HIGH-TEMPERATURE COELECTROLYSIS; HYDROGEN-PRODUCTION; ENERGY; FUELS; STEAM;
D O I
10.1016/j.ijhydene.2013.01.008
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
H2O-CO2 electrochemical conversion in solid oxide electrolysis cells (SOECs) is one of the efficient ways to reduce CO2 emission and to simultaneously store the renewable power. In this study, H2O-CO2 co-electrolysis performance and mechanisms in solid oxide electrolysis button cells at different operating temperature (550-750 degrees C) is tested. The results indicated that the co-electrolysis performance for Ni-YSZ/ScSZ/LSM-ScSZ electrolysis cell increases significantly with temperature. The mass transfer gradually became the rate-determining step of the whole electrodes process below 750 degrees C. By substituting half of the carrier gas to CO2 for the H2O electrolysis system, the electrochemical performance of SOEC became worse, lied between that of H2O and CO2 electrolysis, and was slightly closer to H2O electrolysis at 750 degrees C. CH4 is only detected in the gas products from the reactant composition of 28.6%H2O + 14.3%CO2 + 57.1%Ar, when the operating voltage of the electrolysis cell is higher than 2 V. The CH4 production can be significantly promoted by electricity and can be effectively suppressed by impregnating the anti-carbon deposition catalyst Ru in porous Ni-YSZ cathode. The reactions between carbon element on the electrode surface and hydrogen C(s) + 2H(2) -> CH4 is proposed as one of reaction pathways for CH4 production in H2O-CO2 high temperature co-electrolysis process. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11104 / 11109
页数:6
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