(758d) Design of Highly Active Cobalt Catalysts for CO2 Hydrogenation Via the Tailoring of Surface Orientation of Nanostructures | AIChE

(758d) Design of Highly Active Cobalt Catalysts for CO2 Hydrogenation Via the Tailoring of Surface Orientation of Nanostructures

Authors 

Jimenez, J. - Presenter, Brookhaven Natl Labs
Lauterbach, J., University of South Carolina
One promising route to mitigating CO2 is through the use of point source technologies that upgrade CO2 into high value products via the CO2 hydrogenation mechanism. Due to the high thermodynamic stability of CO2, catalytic routes are often required to convert CO2 into high value products, particularly electrocatalytic and thermo-catalytic processes. The thermo-catalytic approach is often favored due the robust nature of the process, which can be readily scaled to demand and easily integrated into existing point source CO2 sites such as power plants and industrial facilities outfitted with CO2 capture. However, while several advances have been made in the mechanistic understanding of CO2 hydrogenation, there is still need for an applied understanding that can be utilized to create catalyst that selectively favor the preferred product that couples spectroscopic evidence of the reaction intermediates of both the major reaction, and isolated subsequent reaction steps.

In this study, we illustrate how tailoring surface orientations of Co3O4 catalysts on the nanoscale results in control over catalytic performance via the preferential formation of active surface species during CO2 hydrogenation. This resulted in over an order of magnitude increase in the methane turnover frequency on Co3O4 nanorods with the exposed {110}/{001} family of surface facets, as opposed to conventional Co3O4 nanoparticles with the exposed {111}/{001} family of surface facets. We found via in situ DRIFTS studies that this difference in catalytic performance for the Co3O4 nanorods was due to the inhibition of the formate spectator species. Furthermore, by studying the second hydrogenation step in CO2 hydrogenation, which is CO hydrogenation, we were able to discern that the formation of bridged CO was the key difference between the two catalyst. Ultimately, this careful design approach provides a new dimension for the development of next generation catalysts and opens new, more efficient strategies for the conversion of carbon dioxide into useful hydrocarbons.

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