Overconsumption of single-use plastics is creating a global waste catastrophe, with widespread environmental, economic, and health-related consequences. Inspired by the benefits of processive enzyme-catalyzed conversions of biomacromolecules and guided by spectroscopic interrogations of conformation and dynamics of polymer-surface interactions, we have developed the selective hydrogenolysis of high density polyethylene into a narrow distribution of diesel and lubricant-range alkanes catalyzed by an ordered, mesoporous shell/active site/core catalyst architecture. Solid-state nuclear magnetic resonance investigations of polymer chains adsorbed onto solid materials reveal that an appropriately ordered, porous support orients polymer chains into an all-anti conformation, while measurements of polymer dynamics reveal that long hydrocarbon macromolecules readily move within the pores, with a subsequent escape being inhibited by polymer-surface interactions. These interactions and dynamic behavior resemble the binding and translocation of macromolecules in the catalytic cleft of processive enzymes. Thus, transfer of these features to a mesoporous silica material incorporating catalytic platinum sites for carbon-carbon bond hydrogenolysis of polyethylene provides a reliable stream of alkane products through a processive process.

Atomically ordered intermetallic nanoparticles (iNPs) have sparked considerable interest in fuel cell applications by virtue of their exceptional electronic and structural properties. However, the synthesis of small iNPs in a controllable manner remains a formidable challenge because of the high temperature generally required in the formation of intermetallic phases. Here we report a general method for the synthesis of PtZn iNPs (3.2 ± 0.4 nm) on multiwalled carbon nanotubes (MWNT) via a facile and capping agent free strategy using a sacrificial mesoporous silica (mSiO) shell. The as-prepared PtZn iNPs exhibited ca. 10 times higher mass activity in both acidic and basic solution toward the methanol oxidation reaction (MOR) compared to larger PtZn iNPs synthesized on MWNT without the mSiO shell. Density functional theory (DFT) calculations predict that PtZn systems go through a "non-CO" pathway for MOR because of the stabilization of the OH* intermediate by Zn atoms, while a pure Pt system forms highly stable COH* and CO* intermediates, leading to catalyst deactivation. Experimental studies on the origin of the backward oxidation peak of MOR coincide well with DFT predictions. Moreover, the calculations demonstrate that MOR on smaller PtZn iNPs is energetically more favorable than larger iNPs, due to their high density of corner sites and lower-lying energetic pathway. Therefore, smaller PtZn iNPs not only increase the number but also enhance the activity of the active sites in MOR compared with larger ones. This work opens a new avenue for the synthesis of small iNPs with more undercoordinated and enhanced active sites for fuel cell applications.

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Intermetallic compounds are garnering increasing attention as efficient catalysts for improved selectivity in chemical processes. Here, using a ship-in-a-bottle strategy, we synthesize single-phase platinum-based intermetallic nanoparticles (NPs) protected by a mesoporous silica (mSiO 2 ) shell by heterogeneous reduction and nucleation of Sn, Pb, or Zn in mSiO 2 -encapsulated Pt NPs. For selective hydrogenation of furfural to furfuryl alcohol, a dramatic increase in activity and selectivity is observed when intermetallic NPs catalysts are used in comparison to Pt@mSiO 2 . Among the intermetallic NPs, PtSn@mSiO 2 exhibits the best performance, requiring only one-tenth of the quantity of Pt used in Pt@mSiO 2 for similar activity and near 100% selectivity to furfuryl alcohol. A high-temperature oxidation-reduction treatment easily reverses any carbon deposition-induced catalyst deactivation. X-ray photoelectron spectroscopy shows the importance of surface composition to the activity, whereas density functional theory calculations reveal that the enhanced selectivity on PtSn compared to Pt is due to the different furfural adsorption configurations on the two surfaces. ABSTRACT: Intermetallic compounds are garnering increasing attention as efficient catalysts for improved selectivity in chemical processes. Here, using a ship-in-a-bottle strategy, we synthesize single-phase platinum-based intermetallic nanoparticles (NPs) protected by a mesoporous silica (mSiO 2 ) shell by heterogeneous reduction and nucleation of Sn, Pb, or Zn in mSiO 2 -encapsulated Pt NPs. For selective hydrogenation of furfural to furfuryl alcohol, a dramatic increase in activity and selectivity is observed when intermetallic NPs catalysts are used in comparison to Pt@mSiO 2 . Among the intermetallic NPs, PtSn@mSiO 2 exhibits the best performance, requiring only one-tenth of the quantity of Pt used in Pt@mSiO 2 for similar activity and near 100% selectivity to furfuryl alcohol. A hightemperature oxidation−reduction treatment easily reverses any carbon deposition-induced catalyst deactivation. X-ray photoelectron spectroscopy shows the importance of surface composition to the activity, whereas density functional theory calculations reveal that the enhanced selectivity on PtSn compared to Pt is due to the different furfural adsorption configurations on the two surfaces.

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Recently, a facile method for the synthesis of size-monodisperse Pt, Pt Sn, and PtSn intermetallic nanoparticles (iNPs) that are confined within a thermally robust mesoporous silica (mSiO ) shell was introduced. These nanomaterials offer improved selectivity, activity, and stability for large-scale catalytic applications. Here we present the first study of parahydrogen-induced polarization NMR on these Pt-Sn catalysts. A 3000-fold increase in the pairwise selectivity, relative to the monometallic Pt, was observed using the PtSn@mSiO catalyst. The results are explained by the elimination of the three-fold Pt sites on the Pt(111) surface. Furthermore, Pt-Sn iNPs are shown to be a robust catalytic platform for parahydrogen-induced polarization for in vivo magnetic resonance imaging.

Nitrones are key intermediates in organic synthesis and the pharmaceutical industry. The heterogeneous synthesis of nitrones with multifunctional catalysts is extremely attractive but rarely explored. Herein, we report ultrasmall platinum nanoclusters (PtNCs) encapsulated in amine-functionalized Zr metal-organic framework (MOF), UiO-66-NH (Pt@UiO-66-NH ) as a multifunctional catalyst in the one-pot tandem synthesis of nitrones. By virtue of the cooperative interplay among the selective hydrogenation activity provided by the ultrasmall PtNCs and Lewis acidity/basicity/nanoconfinement endowed by UiO-66-NH , Pt@UiO-66-NH exhibits remarkable activity and selectivity, in comparison to Pt/carbon, Pt@UiO-66, and Pd@UiO-66-NH . Pt@UiO-66-NH also outperforms Pt nanoparticles supported on the external surface of the same MOF (Pt/UiO-66-NH ). To our knowledge, this work demonstrates the first examples of one-pot synthesis of nitrones using recyclable multifunctional heterogeneous catalysts.

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