The demand for the development of local laser sintering of nanoparticle arrays is explained by the expanding needs for printed electronics for functional microstructure formation, on heat-sensitive substrates in particular. This work is based on the research into the sintering of arrays of silver nanoparticles synthesized in a spark discharge and deposited on a substrate by focused aerosol flow. The sintering was done by continuous and pulsed lasers with wavelengths 527, 980 and 1054 nm. Sintered samples were studied by measuring the resistivity, cross-section profile area and microstructure features. The highest average conductivity, equal to the half of the bulk silver conductivity, was achieved when sintering by continuous radiation with a wavelength 980 nm. The results showed that when using pulsed radiation the direct heating of nanoparticles in the sample surface layer dominates with the formation of a pore-free conductive layer of around 0.5 μm thick and crystallite of 70–80 nm size. It was found that laser sintering by radiation with a wavelength 527 nm required an order of magnitude lower specific energy costs as compared to the longwave laser radiation. The high energy efficiency of laser sintering is explained by special conditions for radiation absorption at plasmon resonance.
For nanoparticle synthesis in a spark discharge, the influence of the degree of electrode asymmetry in the rod-to-rod configuration, using the example of silver electrodes, on the energy efficiency and nanoparticle composition is studied. The asymmetry degree was determined by the angle between electrodes’ end faces. Two types of discharge current pulses were used: oscillation-damped and unipolar, in which electrodes changed their polarities and had a constant polarity during a single discharge, respectively. A significant influence of the asymmetry degree of the electrode arrangement on the synthesized nanoparticle size, agglomeration and concentration, and on the synthesis energy efficiency, has been established. An increase in the degree of the electrode asymmetry with the oscillation-damped discharge current pulse led to an increased mass production rate and energy efficiency of nanoparticle synthesis, a significant fraction of which had large dimensions of more than 40 nm. The effect of the transfer of synthesized nanoparticles to the opposite electrode at the unipolar discharge current pulse led to the appearance of electroerosive instability, manifested in the formation of a protrusion on the anode surface, around which spark discharges, leading to its further growth and electrode gap closure.
This study investigates the processes of interaction of nanosecond pulsed-periodic laser radiation with the flow of aerosol agglomerates of gold nanoparticles synthesized in a spark discharge. Nanoparticles in a gas flow are spatially separated nano-objects whose interaction with each other and with the walls of an experimental cell was insignificant. Therefore, the energy absorbed by nanoparticles was used only for their own heating with further shape and size modification and on heat transfer to the surrounding gas. In the research, we used laser radiation with wavelengths of 527 and 1053 nm at pulse energies up to 900 µJ and pulse repetition rates up to 500 Hz. The dynamics of changes in the nanoparticles size during their sintering process depending on the laser pulses energy is characterized by an S-shaped shrinkage curve. Complete sintering of the initial agglomerates with their transformation into spherical nanoparticles is achieved by a series of impacting laser pulses. The result of nanoparticles’ laser modification is largely determined by the pulse energy and the efficiency of the nanoparticles’ radiation absorption.
Surface-Enhanced Raman Scattering has been studied for decades as a recognition technique due to its high sensitivity and discriminative power, particularly in biological applications. Inspired by nanopore sequencing technology, we developed a plasmonic device capable of operating in a flow-through configuration to detect individual molecules passing through plasmonic hotspots. This device is a permeable plasmonic film, through which single molecules are sequentially delivered via electrophoresis, while Raman spectra are recorded in real-time. A very effective light-matter coupling, combined with the ultrasmall size of plasmonic spots, enabled access to angstrom spatial and microsecond temporal scales compatible with polymer sequencing. We successfully slowed the translocation process and captured Raman spectra of the four nucleotides at a time resolution down to 20 μs under our experimental conditions. We achieved a discrimination accuracy of 89% at the single-molecule level. Also, we demonstrated a spatial resolution on the order of a few nucleotides, suggesting the potential for sequencing applications.
An analyzed substance’s signal intensity and detection sensitivity in surface-enhanced Raman spectroscopy (SERS) significantly depend on the size and agglomeration degree of nanoparticles (NPs) forming the enhancing structure. Structures were manufactured by aerosol dry printing (ADP), where NPs’ agglomeration depends on printing conditions and additional particle modification techniques. The influence of agglomeration degree on SERS signal enhancement was studied in three types of printed structures using the methylene blue model molecule as an analyte. We demonstrated that the ratio between individual NPs and agglomerates in a studied structure strongly affects SERS signal amplification, and structures formed mainly from non-agglomerated NPs enhance the signal better. In this sense, aerosol NPs modified by pulsed laser radiation provide better results than thermally modified NPs, since in laser modification a larger number of individual NPs is observed due to the absence of secondary agglomeration effects in the gas stream. However, increasing gas flow may minimize the secondary agglomeration, since the time allotted for the agglomeration processes is reduced. In this paper, we show how different NPs’ agglomeration tendencies influence SERS enhancement to demonstrate the process of using ADP to form inexpensive and highly efficient SERS substrates with huge application potential.
In response to the limited environmentally relevant biobased nanoplastic models, the formation of poly(lactic acid) nanoplastics with comparable properties to the ones deriving from the environmental ageing of poly(lactic acid) debris, is presented.