Envisioning quantitative catalytic superiority of interfacial sites in three dimensions

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In the March issue of <i>Chem</i>, Jung and co-workers demonstrated a universal route for identifying the quantitative contribution of active sites in supported catalysts. Combining electronic tomography, catalytic evaluation, and density functional theory (DFT) calculations, the authors provide an analytic approach to correlating reaction pathways with specific active sites for various reactions.