Highly active copper-ceria and copper-ceria-titania catalysts for methanol synthesis from CO2

被引:1192
|
作者
Graciani, Jesus [1 ]
Mudiyanselage, Kumudu [2 ]
Xu, Fang [2 ]
Baber, Ashleigh E. [2 ]
Evans, Jaime [3 ]
Senanayake, Sanjaya D. [2 ]
Stacchiola, Dario J. [2 ]
Liu, Ping [2 ]
Hrbek, Jan [2 ]
Fernandez Sanz, Javier [1 ]
Rodriguez, Jose A. [2 ]
机构
[1] Univ Seville, Dept Phys Chem, E-41012 Seville, Spain
[2] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[3] Cent Univ Venezuela, Fac Ciencias, Caracas 10201, Venezuela
关键词
GAS SHIFT REACTION; MIXED-METAL OXIDE; NANOMETER LEVEL; IN-SITU; WATER; HYDROGENATION; SURFACES; CU; NANOPARTICLES; SPECTROSCOPY;
D O I
10.1126/science.1253057
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
The transformation of CO2 into alcohols or other hydrocarbon compounds is challenging because of the difficulties associated with the chemical activation of CO2 by heterogeneous catalysts. Pure metals and bimetallic systems used for this task usually have low catalytic activity. Here we present experimental and theoretical evidence for a completely different type of site for CO2 activation: a copper-ceria interface that is highly efficient for the synthesis of methanol. The combination of metal and oxide sites in the copper-ceria interface affords complementary chemical properties that lead to special reaction pathways for the CO2 -> CH3OH conversion.
引用
收藏
页码:546 / 550
页数:5
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