• Torelli, Daniel A.
• Liu, Xinyan
• Cummins, Kyle
• Ulissi, Zachary W.
• Nørskov, Jens Kehlet
• Xiao, Jianping
• Tang, Michael T.
• Karamad, Mohammadreza
• Lewis, Nathan S.
• Chan, Karen
• Jaramillo, Thomas F.
• Hahn, Christopher

Abstract

<p>Bimetallic catalysts are promising for the most difficult thermal and electrochemical reactions, but modeling the many diverse active sites on polycrystalline samples is an open challenge. We present a general framework for addressing this complexity in a systematic and predictive fashion. Active sites for every stable low-index facet of a bimetallic crystal are enumerated and cataloged, yielding hundreds of possible active sites. The activity of these sites is explored in parallel using a neural-network-based surrogate model to share information between the many density functional theory (DFT) relaxations, resulting in activity estimates with an order of magnitude fewer explicit DFT calculations. Sites with interesting activity were found and provide targets for follow-up calculations. This process was applied to the electrochemical reduction of CO₂ on nickel gallium bimetallics and indicated that most facets had similar activity to Ni surfaces, but a few exposed Ni sites with a very favorable on-top CO configuration. This motif emerged naturally from the predictive modeling and represents a class of intermetallic CO₂ reduction catalysts. These sites rationalize recent experimental reports of nickel gallium activity and why previous materials screens missed this exciting material. Most importantly these methods suggest that bimetallic catalysts will be discovered by studying facet reactivity and diversity of active sites more systematically.</p>

Topics

• density
• impedance spectroscopy
• surface
• nickel
• theory
• density functional theory
• intermetallic
• Gallium