LAUSR

ConspectusThe rationale of the catalytic activity observed in experiments is a crucial task in fundamental catalysis studies. Efficient catalyst design relies on an accurate understanding of the origin of the activity at the atomic level. Theoretical studies have been widely developed to reach such a fundamental atomic scale understanding of catalytic activity. Current theories ascribe the catalytic activity to the geometric and electronic structure of the active site, in which the geometrical and electronic structure effects are derived from the equilibrium geometry of active sites characterizing the static property of the catalyst; however catalysts, especially in the form of nanoclusters, may present fluxional and dynamic structure under reaction conditions, and the effect of this fluxional behavior is not yet widely recognized. Therefore, this Account will focus on the fluxionality of the active sites, which is driven by thermal fluctuations under finite temperature.Under reaction conditions, nanocluster catalysts can readily restructure, either being promoted to another metastable isomer (named as plastic fluxionality) or presenting ample deformations around their equilibrium geometry (named as elastic fluxionality). This Account summarizes our recent studies on the fluxionality of the nanoclusters and how plastic and elastic fluxionalities play roles in highly efficient reaction pathways. Our results show that the low energy metastable isomers formed by plastic fluxionality can manifest high reactivity despite their minor occurrence probability in the mixture of catalyst isomers. In the end, the highly active metastable isomer may dominate the total observed reactivity. In addition, the isomerization between the global minimum structure and the highly active metastable isomer can be a central step in catalytic transformations in order to circumvent some difficult reaction steps and may govern the overall mechanism. In addition, the thermal fluctuation driven elastic fluxionality is also found to play a key role, complementary to plastic fluxionality. The elastic fluxionality creates substantial structural deformations of the active site, and these deformed geometries enable low activation energies and high catalytic activity, which cannot be found from the static equilibrium geometry of the catalyst. A dedicated global activity search algorithm is proposed to search for the optimal reaction pathway on fluxional nanoclusters. In summary, our studies demonstrate that thermal-driven fluxionality provides a different paradigm for understanding the high activity of nanoclusters under reaction conditions beyond the static description of geometric and electronic structure. We first summarize our previous results and then provide a perspective for further studies on how to investigate and take the advantage of the fluxional geometry of nanoclusters. We will defend in this Account that the static picture for the active site is not complete and might miss critical reaction pathways that are highly efficient and only open after thermally induced restructuring of the active site.