Tuning Catalytic Selectivity At The Mesoscale Via Interparticle Interactions
Keywords
CO; CO electroreduction 2; copper; electrocatalysis; methane; nanoparticles
Abstract
The selectivity of heterogeneously catalyzed chemical reactions is well-known to be dependent on nanoscale determinants, such as surface atomic geometry and composition. However, principles to control the selectivity of nanoparticle (NP) catalysts by means of mesoscopic descriptors, such as the interparticle distance, have remained largely unexplored. We used well-defined copper catalysts to deconvolute the effect of NP size and distance on product selectivity during CO2 electroreduction. Corroborated by reaction-diffusion modeling, our results reveal that mesoscale phenomena such as interparticle reactant diffusion and readsorption of intermediates play a defining role in product selectivity. More importantly, this study uncovers general principles of tailoring NP activity and selectivity by carefully engineering size and distance. These principles provide guidance for the rational design of mesoscopic catalyst architectures in order to enhance the production of desired reaction products.
Publication Date
2-5-2016
Publication Title
ACS Catalysis
Volume
6
Issue
2
Number of Pages
1075-1080
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1021/acscatal.5b02202
Copyright Status
Unknown
Socpus ID
84957582149 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/84957582149
STARS Citation
Mistry, Hemma; Behafarid, Farzad; Reske, Rulle; Varela, Ana Sofia; and Strasser, Peter, "Tuning Catalytic Selectivity At The Mesoscale Via Interparticle Interactions" (2016). Scopus Export 2015-2019. 2545.
https://stars.library.ucf.edu/scopus2015/2545