3D Hybrid Trilayer Heterostructure: Tunable Au Nanorods and Optical Properties.

Engineering plasmonic nanostructures from three dimensions (3D) is very attractive toward controllable and tunable nanophotonic components and devices. Herein, Au-based trilayer heterostructures composed of a dielectric spacer sandwiched by hybrid Au-TiN vertically aligned nanocomposite (VAN) nanoplasmonic claddings are demonstrated with a broad range of geometries and property tuning. Two types of spacer layers, that is, a pure dielectric BaTiO3 layer and a hybrid plasmonic Au-BaTiO3 VAN layer, contribute to the tuning of the Au nanorod dimension. Such geometrical variations of Au nanostructures originate from the surface energy and lattice strain tuned by the spacer layers. Optical measurements and numerical simulations suggest the change of the localized surface plasmon resonance which is strongly affected by the tailored Au nanorods as either separated or channeled. The uniaxial dielectric tensors suggest a tunable hyperbolic property affected by such a metal-insulator-metal trilayer stack. The complex 3D heterostructures offer additional tuning parameters and design flexibilities in hybrid plasmonic metamaterials toward potential applications in light harvesting, sensing, and nanophotonic devices.

Catalytic activity of bimetallic catalysts highly sensitive to the atomic composition and phase structure at the nanoscale.

The ability to determine the atomic arrangement in nanoalloy catalysts and reveal the detailed structural features responsible for the catalytically active sites is essential for understanding the correlation between the atomic structure and catalytic properties, enabling the preparation of efficient nanoalloy catalysts by design. Herein we describe a study of CO oxidation over PdCu nanoalloy catalysts focusing on gaining insights into the correlation between the atomic structures and catalytic activity of nanoalloys. PdCu nanoalloys of different bimetallic compositions are synthesized as a model system and are activated by a controlled thermochemical treatment for assessing their catalytic activity. The results show that the catalytic synergy of Pd and Cu species evolves with both the bimetallic nanoalloy composition and temperature of the thermochemical treatment reaching a maximum at a Pd : Cu ratio close to 50 : 50. The nanoalloys are characterized structurally by ex situ and in situ synchrotron X-ray diffraction, including atomic pair distribution function analysis. The structural data show that, depending on the bimetallic composition and treatment temperature, PdCu nanoalloys adopt two different structure types. One features a chemically ordered, body centered cubic (B2) type alloy consisting of two interpenetrating simple cubic lattices, each occupied with Pd or Cu species alone, and the other structure type features a chemically disordered, face-centered cubic (fcc) type of alloy wherein Pd and Cu species are intermixed at random. The catalytic activity for CO oxidation is strongly influenced by the structural features. In particular, it is revealed that the prevalence of chemical disorder in nanoalloys with a Pd : Cu ratio close to 50 : 50 makes them superior catalysts for CO oxidation in comparison with the same nanoalloys of other bimetallic compositions. However, the catalytic synergy can be diminished if the Pd50Cu50 nanoalloys undergo phase segregation into distinct chemically-ordered (B2-type) and disordered (fcc-type) domains. This finding is significant since it provides a rational basis for streamlining the design and preparation of Pd-based nanoalloy catalysts in terms of atomic structure and phase state.

Nanoalloying and phase transformations during thermal treatment of physical mixtures of Pd and Cu nanoparticles.

Nanoscale alloying and phase transformations in physical mixtures of Pd and Cu ultrafine nanoparticles are investigated in real time with in situ synchrotron-based x-ray diffraction complemented by ex situ high-resolution transmission electron microscopy. The combination of metal-support interaction and reactive/non-reactive environment was found to determine the thermal evolution and ultimate structure of this binary system. At 300 °C, the nanoparticles supported on silica and carbon black intermix to form a chemically ordered CsCl-type (B2) alloy phase. The B2 phase transforms into a disordered fcc alloy at higher temperature (> 450 °C). The alloy nanoparticles supported on silica and carbon black are homogeneous in volume, but evidence was found of Pd surface enrichment. In sharp contrast, when supported on alumina, the two metals segregated at 300 °C to produce almost pure fcc Cu and Pd phases. Upon further annealing of the mixture on alumina above 600 °C, the two metals interdiffused, forming two distinct disordered alloys of compositions 30% and 90% Pd. The annealing atmosphere also plays a major role in the structural evolution of these bimetallic nanoparticles. The nanoparticles annealed in forming gas are larger than the nanoparticles annealing in helium due to reduction of the surface oxides that promotes coalescence and sintering.

Harnessing molecule-solid duality of nanoclusters/nanoparticles for nanoscale control of size, shape and alloying.

This report demonstrates a molecule-solid duality concept for nanoscale control of size, shape and alloying by showing novel evolution of binary copper and gold nanoclusters or nanoparticles towards alloy nanocubes, as evidenced by in situ real time synchrotron X-ray diffraction characterization.