Methane synthesis from CO2 and H2O using a phosphate-based electrochemical cell at 210-270 °C with oxide-supported Ru catalysts

被引:6
作者
Kubota, Jun [1 ]
Okumura, Takaya [1 ]
Hayashi, Rika [1 ]
机构
[1] Fukuoka Univ, Dept Chem Engn, Jonan Ku, 8-19-1 Nanakuma, Fukuoka 8140180, Japan
关键词
HYDROGEN SPILLOVER; AMMONIA-SYNTHESIS; CARBON-MONOXIDE; METAL; MEMBRANE; ELECTROLYSIS; TEMPERATURE; ELECTRICITY; ADSORPTION; REDUCTION;
D O I
10.1039/d1se02029c
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
The conversion of electricity to chemical energy is a key technology for absorbing the fluctuations of electricity and utilizing solar and wind-powered electricities as chemical fuels. An electrochemical system equipped with a phosphate-based electrolyte has been reported as a promising method to efficiently obtain CH4 from CO2 and H2O in a single electrochemical cell. Electrochemical cells with 10 wt%-Ru/ZrO2, Ru/Al2O3, and Ru/TiO2 were examined for CH4 synthesis from CO2 and H2O at 210-270 degrees C and 10 mA cm(-2). Approximately 13 and 1 nmol s(-1) cm(-2) of CH4 and H-2, respectively, were formed using the Ru/ZrO2 cell at 270 degrees C, and the current efficiencies for CH4 and H-2 formation were 97 and 3%, respectively. The cells with Ru/Al2O3 and Ru/TiO2 produced lower CH4 yields. An H-permeable membrane (Pd-Ag) cathode cell, which was designed in a previous study, and a newly designed PTFE membrane filter cell was investigated with Ru/ZrO2. Both cells demonstrated similar formation rates and current efficiencies, which means that the Pd-Ag membrane is not essential for the synthesis of CH4 from CO2 and H2O. The catalysts were analyzed using transmission electron microscopy and temperature-programmed desorption of H-2.
引用
收藏
页码:1362 / 1372
页数:11
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