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Plastics, of the order of microns in size, being not visible to the naked eye, are one of the significant contributors to pollution in the environment. Thus, the detection of micron-sized plastics (microplastics (MPs)) is crucial because of its hazardous toxic effects on our surroundings. In this work, we have proposed a quick and on-site detection of MPs, such as, polyvinyl chloride (PVC), polyvinyl alcohol (PVA) and polystyrene (PS) at ultra trace level using surface-enhanced Raman spectroscopy (SERS). To detect and analyse the spectra, two different nanostructures, such as, spherical shaped Ag nanoparticles (NPs), and shape anisotropic Ag nano-dendrites (NDs) were utilised to acquire the SERS spectra. A comprehensive analysis was further performed to check and investigate the amount of enhancements due to the mentioned nanostructures. We observed the Ag NDs exhibited amplified signal intensity compared to the Ag NPs due to the shape anisotropy leading to the surface charge confinement effect to create highly dense hotspots. However, the spherical shaped polystyrene beads of micron size exhibited better enhancement in Raman signal intensity when mixed with Ag NPs due to increased surface adsorption with the NPs. Therefore, the comparative study emphasizes the ability of using solution-based nanostructure as SERS for the onsite detection of microplastics having diverge size range at low concentration., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Programmable nanoscale carriers, such as liposomes and DNA, are readily being explored for personalized medicine or disease prediction and diagnostics. The characterization of these nanocarriers is limited and challenging due to their complex chemical composition. Here, we demonstrate the utilization of surface-enhanced Raman spectroscopy (SERS), which provides a unique molecular fingerprint of the analytes while reducing the detection limit. In this paper, we utilize a silver coated nano-bowl shaped polydimethylsiloxane (PDMS) SERS substrate. The utilization of nano-bowl surface topology enabled the passive trapping of particles by reducing mobility, which results in reproducible SERS signal enhancement. The biological nanoparticles' dwell time in the nano-trap was in the order of minutes, thus allowing SERS spectra to remain in their natural aqueous medium without the need for drying. First, the geometry of the nano-traps was designed considering nanosized bioparticles of 50-150 nm diameter. Further, the systematic investigation of maximum SERS activity was performed using rhodamine 6 G as a probe molecule. The potential of the optimized SERS nano-bowl is shown through distinct spectral features following surface- (polyethylene glycol) and bilayer- (cholesterol) modification of empty liposomes of around 140 nm diameter. Apart from liposomes, the characterization of the highly crosslinked DNA specimens of only 60 nm in diameter was performed. The modification of DNA gel by liposome coating exhibited unique signatures for nitrogenous bases, sugar, and phosphate groups. Further, the unique sensitivity of the proposed SERS substrate displayed distinct spectral signatures for DNA micelles and drug-loaded DNA micelles, carrying valuable information to monitor drug release. In conclusion, the findings of the spectral signatures of a wide range of molecular complexes and chemical morphology of intra-membranes in their natural state highlight the possibilities of using SERS as a sensitive and instantaneous characterization alternative., Competing Interests: The authors declare no conflicts of interest., (© 2024 Optica Publishing Group.)

Antimicrobial resistance (AMR) is a major health threat worldwide and the culture-based bacterial detection methods are slow. Surface-enhanced Raman spectroscopy (SERS) can be used to identify target analytes in real time with sensitivity down to the single-molecule level, providing a promising solution for the culture-free bacterial detection. We report the fabrication of SERS substrates having tightly packed silver (Ag) nanoparticles loaded onto long silicon nanowires (Si NWs) grown by the metal-assisted chemical etching (MACE) method for the detection of bacteria. The optimized SERS chips exhibited sensitivity down to 10 -12 M concentration of R6G molecules and detected reproducible Raman spectra of bacteria down to a concentration of 100 colony forming units (CFU)/mL, which is a thousand times lower than the clinical threshold of bacterial infections like UTI (10 5 CFU/mL). A Siamese neural network model was used to classify SERS spectra from bacteria specimens. The trained model identified 12 different bacterial species, including those which are causative agents for tuberculosis and urinary tract infection (UTI). Next, the SERS chips and another Siamese neural network model were used to differentiate AMR strains from susceptible strains of Escherichia coli ( E. coli ). The enhancement offered by SERS chip-enabled acquisitions of Raman spectra of bacteria directly in the synthetic urine by spiking the sample with only 10 3 CFU/mL E. coli . Thus, the present study lays the ground for the identification and quantification of bacteria on SERS chips, thereby offering a potential future use for rapid, reproducible, label-free, and low limit detection of clinical pathogens.

The thermal evaporation method can easily be employed to fabricate hybrid inorganic-organic LEDs and the emission properties can be controlled by varying the thickness of the nanocrystalline CdTe film. The fabrication of CdTe nanocrystals on glass substrates was demonstrated using a thermal evaporation method. Films were characterised using various experimental tools, such as SEM, TEM, AFM, UV-Vis and PL spectroscopy. The formation of nanoparticles with diameters from 1.5 nm up to 9 nm was observed in the nanocrystalline thin films. The organic light emitting diodes (OLEDs) based on these nanocrystals as an emissive layer exhibit electroluminescence (EL) in the green to yellow region of the visible spectrum, which is ascribed to the varying size dependent EL from the nanocrystals of CdTe present in the thin film. The method demonstrates an easy and convenient way to incorporate inorganic CdTe nanocrystals inside the organic light emitting devices., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

We report the fabrication of low cost highly structured silver (Ag) capped aluminium (Al) nanorods (NRs) as surface enhanced Raman spectroscopy (SERS) substrate utilising the glancing angle deposition technique. The nano-capping of silver onto the Al NRs can concentrate the local electric field within the minimal volume that can serve as hotspots. The average size of the Ag nanocaps was 50 nm. The newly proposed nanoporous Ag capped Al NRs as SERS substrate could detect the Raman signal of rhodamine 6G (R6G) up to 10 -15 molar concentration. The significant enhancement in the Raman signal of 10 7 was achieved for Ag capped Al NRs considering R6G as a probe molecule. Using the developed SERS substrate, we recorded Raman spectra for Escherichia coli bacteria with its concentration varying from 10 8 colony forming units per ml (CFU ml -1 ) up to 10 2 CFU ml -1 . All the reported Raman spectra were acquired by a portable handheld Raman spectrometer. Hence, this newly proposed low cost, effective SERS substrate can be used commercially for the onsite detection of clinical pathogens. The 3D finite difference time domain simulation model was performed for Ag capped Al nanostructure to understand the generation of hotspots. The simulated results show excellent agreement with the experimental results. We fabricated uncapped Ag nanorods of similar dimensions and performed the experimental measurements and simulations for comparison. We found a significant enhancement in Ag capped Al NRs compared to the long Ag NRs. The description of the Raman signal enhancement has been elaborated., (© 2021 IOP Publishing Ltd.)