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Plastic pollution is a major environmental and health threat due to its widespread presence in ecosystems and food chains. Despite extensive research on microplastics, the detection of submicron plastics remains challenging due to their distinct physical and chemical properties and the limitations of current analytical methods. SERS has attracted significant attention in recent research as an ultra-sensitive approach for detecting nanoplastics compared to other spectroscopy techniques. In this paper, a stable, biodegradable, waste-free novel paper-based SERS substrate is developed for the rapid detection of submicron (200 nm) polystyrene (PS) particles via the controlled deposition of AuNPs onto filter paper using an atmospheric cold plasma jet printing process. The density of AuNPs increases with the number of printing passes, correlating with enhanced SERS results. The resulting SERS substrates are capable of quantifying a broad range of PS concentrations (1–500 μg mL⁻¹) using just 5 μL of analyte. The fabricated SERS substrate enables reliable quantification of PS in water, exhibiting a strong linear correlation (R² = 0.993) between SERS intensity and PS concentration, with a detection limit of 10 μg mL⁻¹ . These substrates demonstrate exceptional stability and reproducibility over a 10-week period, addressing key challenges associated with paper-based SERS substrates and making them suitable for long-term monitoring. Furthermore, analysis of tap water as a representative real-world sample demonstrates the practical applicability of the SERS substrate for environmental monitoring, revealing quantifiable levels of PS contamination. 

The widespread industrial and consumer use of per- and polyfluoroalkyl substances (PFAS) has led to their persistent presence in the environment, driven by their robust carbon-fluorine bonds and bioaccumulative properties. This contamination poses serious health and ecological risks, making real-time, selective, and sensitive detection of PFAS critical for effective mitigation. We demonstrate a selective and sensitive detection of vapor-phase PFAS using photothermal cantilever deflection spectroscopy (PCDS), achieving a detection limit of ∼30 pg. This method eliminates the need for chemically selective coatings, relying instead on the physisorption of PFAS molecules onto a bi-material microcantilever. By leveraging mid-infrared absorption and monitoring both cantilever bending and resonance frequency, PCDS enables simultaneous chemical identification and mass quantification. The technique demonstrates high selectivity in the mid-infrared fingerprint region and rapid desorption of analytes, offering significant advantages for real-time environmental monitoring and public health protection. 

An accurate molecular identification of plastic waste is important in increasing the efficacy of automatic plastic sorting in recycling. However, identification of real-world plastic waste, according to their resin identification code, remains challenging due to the lack of techniques that can provide high molecular selectivity. In this study, a standoff photothermal spectroscopy technique, utilizing a microcantilever, was used for acquiring mid-infrared spectra of real-world plastic waste, including those with additives, surface contaminants, and mixed plastics. Analysis of the standoff spectral data, using Convolutional Neural Network (CNN), showed 100% accuracy in selectively identifying real-world plastic waste according to their respective resin identification codes. Standoff photothermal spectroscopy, together with CNN analysis, offers a promising approach for the selective characterization of waste plastics in Material Recovery Facilities (MRFs). 

Molecular-level spectroscopy is crucial for sensing and imaging applications, yet detecting and quantifying minuscule quantities of chemicals remains a challenge, especially when they surface-adsorb in low numbers. Here, we introduce a photothermal spectroscopic technique that enables the sensing and quantification of adsorbates with an attogram detection limit. Our approach utilizes the Seebeck effect in a microfabricated nanoscale thermocouple junction, incorporated into the apex of a microcantilever. We observe minimal thermal mass exhibited by the sensor which maintains exceptional thermal insulation. The temperature variation driving the thermoelectric junction arises from the non-radiative decay of molecular adsorbates' vibrational states on the tip. We demonstrate the detection of physisorbed trinitrotoluene (TNT) and dimethyl methylphosphonate (DMMP) molecules, as well as representative polymers, with an estimated mass sensitivity of 10-18 g and a temperature resolution of 40 mK. 

Standoff detection based on optical spectroscopy is an attractive method for identifying materials at a distance with very high molecular selectivity. Standoff spectroscopy can be exploited in demanding practical applications such as sorting plastics for recycling. Here, we demonstrate selective and sensitive standoff detection of polymer films using bi-material cantilever-based photothermal spectroscopy. We demonstrate that the selectivity of the technique is sufficient to discriminate various polymers. We also demonstrate in situ, point detection of thin layers of polymers deposited on bi-material cantilevers using photothermal spectroscopy. Comparison of the standoff spectra with those obtained by point detection, FTIR, and FTIR-ATR show relative broadening of peaks. Exposure of polymers to UV radiation (365 nm) reveal that the spectral peaks do not change with exposure time, but results in peak broadening with an overall increase in the background cantilever response. The sensitivity of the technique can be further improved by optimizing the thermal sensitivity of the bi-material cantilever and by increasing the number of photons impinging on the cantilever. 

Abstract Gallium‐based liquid metals (LMs) are widely used for stretchable and reconfigurable electronics thanks to their fluidic nature and excellent conductivity. These LMs possess attractive optical properties for photonics applications as well. However, due to the high surface tension of the LMs, it is challenging to form LM nanostructures with arbitrary shapes using conventional nanofabrication techniques. As a result, LM‐based nanophotonics has not been extensively explored. Here, a simple yet effective technique is demonstrated to deterministically fabricate LM nanopatterns with high yield over a large area. This technique demonstrates for the first time the capability to fabricate LM nanophotonic structures of various precisely defined shapes and sizes using two different LMs, that is, liquid gallium and liquid eutectic gallium–indium alloy. High‐density arrays of LM nanopatterns with critical feature sizes down to ≈100 nm and inter‐pattern spacings down to ≈100 nm are achieved, corresponding to the highest resolution of any LM fabrication technique developed to date. Additionally, the LM nanopatterns demonstrate excellent long‐term stability under ambient conditions. This work paves the way toward further development of a wide range of LM nanophotonics technologies and applications.