Heat-induced morphological changes in silver nanowires deposited on a patterned silicon substrate.

Metallic nanowires (NWs) are sensitive to heat treatment and can split into shorter fragments within minutes at temperatures far below the melting point. This process can hinder the functioning of NW-based devices that are subject to relatively mild temperatures. Commonly, heat-induced fragmentation of NWs is attributed to the interplay between heat-enhanced diffusion and Rayleigh instability. In this work, we demonstrated that contact with the substrate plays an important role in the fragmentation process and can strongly affect the outcome of the heat treatment. We deposited silver NWs onto specially patterned silicon wafers so that some NWs were partially suspended over the holes in the substrate. Then, we performed a series of heat-treatment experiments and found that adhered and suspended parts of NWs behave differently under the heat treatment. Moreover, depending on the heat-treatment process, fragmentation in either adhered or suspended parts can dominate. Experiments were supported by finite element method and molecular dynamics simulations.

Deposition of low-density thick silica films from burning sol-gel derived alcogels.

In the current study we show that the combustion of sol-gel derived alcogels with specifically tailored composition leads to the release of silica nanoparticles from the burning alcogel in a controlled manner which enables direct deposition of the released nanoparticles into low-density silica thick films. The process has some similarities to flame spray pyrolysis but requires no aerosol generator or other sophisticated instrumental setup. By the proper choice of catalysts and mixture of silicon alkoxides for the synthesis of the alcogel, preferential hydrolysis and polycondensation of one of the alkoxides is achieved. This leads to the formation of an alcogel with volatile silica precursor trapped in the gel pores. Resulting alcogels were burned to deposit uniform porous silica films with density of ~0.1 g/cm3 and primary particle size of ~10 nm. Demonstrated method yields silanol-free silica directly, without additional treatment steps and enables straightforward control over the deposition rate and coarseness of the layer by simple adjustment of the composition of the silica alcogel. The maximum layer thickness is limited only by the deposition time (in the current work up to 134 µm). Such technique of porous oxide film preparation could potentially be extended to the preparation of porous films from other oxides by using respective metal alkoxides as precursors.

Plasmonic nanostructures through DNA-assisted lithography.

Programmable self-assembly of nucleic acids enables the fabrication of custom, precise objects with nanoscale dimensions. These structures can be further harnessed as templates to build novel materials such as metallic nanostructures, which are widely used and explored because of their unique optical properties and their potency to serve as components of novel metamaterials. However, approaches to transfer the spatial information of DNA constructions to metal nanostructures remain a challenge. We report a DNA-assisted lithography (DALI) method that combines the structural versatility of DNA origami with conventional lithography techniques to create discrete, well-defined, and entirely metallic nanostructures with designed plasmonic properties. DALI is a parallel, high-throughput fabrication method compatible with transparent substrates, thus providing an additional advantage for optical measurements, and yields structures with a feature size of ~10 nm. We demonstrate its feasibility by producing metal nanostructures with a chiral plasmonic response and bowtie-shaped nanoantennas for surface-enhanced Raman spectroscopy. We envisage that DALI can be generalized to large substrates, which would subsequently enable scale-up production of diverse metallic nanostructures with tailored plasmonic features.

Gilded nanoparticles for plasmonically enhanced fluorescence in TiO2:Sm3+ sol-gel films.

Silica-gold core-shell nanoparticles were used for plasmonic enhancement of rare earth fluorescence in sol-gel-derived TiO2:Sm3+ films. Local enhancement of Sm3+ fluorescence in the vicinity of separate gilded nanoparticles was revealed by a combination of dark field microscopy and fluorescence spectroscopy techniques. An intensity enhancement of Sm3+ fluorescence varies from 2.5 to 10 times depending on the used direct (visible) or indirect (ultraviolet) excitations. Analysis of fluorescence lifetimes suggests that the locally stronger fluorescence occurs because of higher plasmon-coupled direct absorption of exciting light by the Sm3+ ions or due to plasmon-assisted non-radiative energy transfer from the excitons of TiO2 host to the rare earth ions. PACS: 78; 78.67.-n; 78.67.Bf.