Surface Protonics Promotes Catalysis

被引:77
作者
Manabe, R. [1 ]
Okada, S. [1 ]
Inagaki, R. [1 ]
Oshima, K. [2 ]
Ogo, S. [1 ]
Sekine, Y. [1 ]
机构
[1] Waseda Univ, Appl Chem, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
[2] Numazu Coll, Chem & Biochem, Natl Inst Technol, 3600 Ooka, Shizuoka 4108501, Japan
关键词
TEMPERATURE HYDROGEN-PRODUCTION; SYNTHESIS GAS; CHEMICAL CONVERSION; KINETIC ASSESSMENT; SITE REQUIREMENTS; PARTIAL OXIDATION; REACTION PATHWAYS; NICKEL-CATALYSTS; METHANE; CARBON;
D O I
10.1038/srep38007
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Catalytic steam reforming of methane for hydrogen production proceeds even at 473 K over 1 wt% Pd/CeO2 catalyst in an electric field, thanks to the surface protonics. Kinetic analyses demonstrated the synergetic effect between catalytic reaction and electric field, revealing strengthened water pressure dependence of the reaction rate when applying an electric field, with one-third the apparent activation energy at the lower reaction temperature range. Operando-IR measurements revealed that proton conduction via adsorbed water on the catalyst surface occurred during electric field application. Methane was activated by proton collision at the Pd-CeO2 interface, based on the inverse kinetic isotope effect. Proton conduction on the catalyst surface plays an important role in methane activation at low temperature. This report is the first describing promotion of the catalytic reaction by surface protonics.
引用
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页数:7
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