Journal
ADVANCED MATERIALS INTERFACES
Volume 10, Issue 4, Pages -Publisher
WILEY
DOI: 10.1002/admi.202202368
Keywords
density functional theory; electronic localization function; H-2 production; layered silicate; palladium nanoparticle
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In order to maximize the surface-to-body ratio, it is necessary to use smaller metallic palladium nanoparticles for catalytic applications. However, if the supported palladium is below a critical size, the hybridization with the supporting material can decrease the labile electrons that are crucial for catalytic reactions. It has been demonstrated that palladium with at least six atomic layers on silicate sheets exhibits a metallic-like electronic property, resulting in excellent catalytic activity compared to isotropic palladium nanoparticles and single-atom palladium.
Maximizing surface-to-body ratio demands ever smaller metallic palladium (Pd) nanoparticles for catalytic applications. The quest for miniaturization is now reaching the single-atom limit. However, if the supported Pd is below a critical size, the Pd hybridization with the supporting material can detrimentally reduce the labile electrons that facilitate the catalytic reactions. Thus, the smallest attainable size, i.e., single-atom Pd, may not offer the best efficiency. Here, it is demonstrated that Pd with at least six atomic layers (or thickness of approximate to 1 nm) on the silicate sheets, synthesized via the partial exfoliation of a layered silicate, exhibits a metallic-like electronic property, yielding an excellent catalytic activity (e.g., turnover frequency) for dehydrogenating formic acid higher than both isotropic Pd nanoparticles and single-atom Pd.
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