Gas-to-nanotextile: high-performance materials from floating 1D nanoparticles.

Suspended in the gas phase, 1D inorganic nanoparticles (nanotubes and nanowires) grow to hundreds of microns in a second and can be thus directly assembled into freestanding network materials. The corresponding process continuously transforms gas precursors into aerosols into aerogels into macroscopic nanotextiles. By enabling the assembly of very high aspect ratio nanoparticles, this processing route has translated into high-performance structural materials, transparent conductors and battery anodes, amongst other embodiments. This paper reviews progress in the application of such manufacturing process to nanotubes and nanowires. It analyses 1D nanoparticle growth through floating catalyst chemical vapour deposition (FCCVD), in terms of reaction selectivity, scalability and its inherently ultra-fast growth rates (107-108 atoms per second) up to 1000 times faster than for substrate CVD. We summarise emerging descriptions of the formation of aerogels through percolation theory and multi-scale models for the collision and aggregation of 1D nanoparticles. The paper shows that macroscopic ensembles of 1D nanoparticles resemble textiles in their porous network structure, high flexibility and damage-tolerance. Their bulk properties depend strongly on inter-particle properties and are dominated by alignment and volume fraction. Selected examples of nanotextiles that surpass granular and monolithic materials include structural fibres with polymer-like toughness, transparent conductors, and slurry-free composite electrodes for energy storage.

Controlling reaction paths for ultra-fast growth of inorganic nanowires floating in the gas phase.

Synthesis of inorganic nanowires/nanotubes suspended in the gas through floating catalyst chemical vapour deposition (FCCVD) produces exceptional growth rates of 5-1000 micron per second, several orders of magnitude faster than conventional substrate processes. It leads to nanowire lengths >100 microns and thus to the possibility of direct assembly into freestanding macroscopic networks as a continuous process. This work studies the different reaction paths controlling conversion and selectivity in FCCVD applied to the synthesis of silicon nanowires (SiNWs) from silane, grown through an aerosol of gold catalyst nanoparticles. There are two main competing reactions: catalysed growth of SiNWs and non-catalysed formation of amorphous Si nanoparticles. The mass fraction of the two populations can be precisely determined by XRD and Raman spectroscopy, enabling high-throughput screening of reaction parameter space. The experimental data and accompanying analytical model show that selectivity is kinetically controlled by the ratio of precursor/hydrogen carrier gas, through its inhibition of the pyrolisis of silane into silylene. In contrast, the rate of SiNW growth is largely unaffected by hydrogen and not limited by precursor availability. These results provide a framework to describe the kinetics of nanomaterials growth by FCCVD.