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Michael A. Filler

Publications and source records attributed to Michael A. Filler.

4 recordsLinked to original sources

Synthesis and guided assembly of niobium trisulfide nanowires and nanowire chains by chemical vapor deposition

One-dimensional (1D) nanostructures of transition metal trichalcogenides (TMT) show unique properties through the combination of their anisotropic bonding and low dimensionality. Scalable synthesis approaches that enable control over the morphology, dimensions, and interfaces of 1D TMTs with other nanoscale materials could allow these properties to be used in novel devices. Here, we report chemical vapor deposition of a 1D TMT, namely niobium trisulfide (NbS3) in the form of nanowires, on different substrates, including bulk substrates (amorphous SiO2/Si and crystalline c-sapphire) and several two-dimensional (2D) van der Waals materials (graphene, h-BN, CrSBr). We demonstrate high growth yield with axial growth rates of up to 40 micrometer/min and with two different growth modes: short nanowires of rectangular cross-section, and unusual long, "chained nanowires" up to 100 micrometer in length with sawtooth morphology. We discuss a mechanism that accounts for the two morphologies and discuss how the structure can be tuned through substrate choice and growth conditions. We further demonstrate guided assembly at the edges of graphene and h-BN, as well as epitaxial growth on few-layer CrSBr and c-sapphire. These results open pathways to explore scalable synthesis and directed assembly of 1D TMT nanomaterials in unique morphologies.

cond-mat.mtrl-sci

Salt-assisted vapor-liquid-solid growth of one-dimensional van der Waals materials

We have combined the benefits of two catalytic growth phenomena to form nanostructures of transition metal trichalcogenides (TMTs), materials that are challenging to grow in a nanostructured form by conventional techniques, as required to exploit their exotic physics. Our growth strategy combines the benefits of vapor-liquid-solid (VLS) growth in controlling dimension and growth location, and salt-assisted growth for fast growth at moderate temperatures. This salt-assisted VLS growth is enabled through use of a catalyst that includes Au and an alkali metal halide. We demonstrate high yields of NbS3 1D nanostructures with sub-ten nanometer diameter, tens of micrometers length, and distinct 1D morphologies consisting of nanowires and nanoribbons with [010] and [100] growth orientations, respectively. We present strategies to control the growth location, size, and morphology. We extend the growth method to synthesize other TMTs, NbSe3 and TiS3, as nanowires. Finally, we discuss the growth mechanism based on the relationships we measure between the materials characteristics (growth orientation, morphology and dimensions) and the growth conditions (catalyst volume and growth time). Our study introduces opportunities to expand the library of emerging 1D vdW materials and their heterostructures with controllable nanoscale dimensions.

cond-mat.mtrl-sci

One-Dimensional Twisted and Tubular Structures of Zinc Oxide by Semiconductor-Catalyzed Vapor-Liquid-Solid Synthesis

The exploration of new catalysts for the vapor-liquid-solid (VLS) synthesis of one-dimensional (1-D) materials promises to yield new morphologies and functionality. Here, we show, for the model ZnO system, that this possible using a semiconductor (Ge) catalyst. In particular, two unusual morphologies are described: twisted nanowires and twisted nanotubes, in addition to the usual straight nanowires. The twisted nanotubes show large hollow cores and surprisingly high twisting rates (up to 9o/μm), which cannot be easily explained through the Eshelby twist model. A combination of ex situ and in situ transmission electron microscopy measurements suggest that the hollow core results from a competition between growth and etching at the Ge-ZnO interface during synthesis. The twisting rate is consistent with a softening of elastic rigidity. These results indicate that the use of unconventional, nonmetallic catalysts provide opportunities to synthesize unusual oxide structures with potentially useful properties.

cond-mat.mtrl-sci

Photonic thermal conduction by infrared plasmonic resonators in semiconductor nanowires

Photons typically do not contribute to thermal transport within a solid due to their low energy density and tendency to be quickly absorbed. We propose a practical material system - infrared plasmonic resonators embedded in a semiconductor nanowire - that leverages near-field electromagnetic coupling to achieve photonic thermal transport comparable to the electronic and phononic contributions. We analytically show photonic thermal conductivities up to about 1 W m-1 K-1 for 10 nm diameter Si and InAs nanowires containing repeated resonators at 500 K. The nanowire system outperforms plasmonic particles in isotropic environments and presents a pathway for photonic thermal transport to exceed that of phonons and electrons.

cond-mat.mes-hall