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Using strong ligand as morphology directing agent, AuNPs with sheet-like surface sub-structures were successfully synthesized. Arising from the continuous tuning of the strong ligand control, the surface roughness of the AuNPs can be continuously tuned, so thus the LSPR and SERS. [Display omitted] In this work, we reported that by using a strong thiol ligand as the morphology-directing reagent, a series of Au nanoparticles with plate-like surface sub-structures could be successfully obtained via a one-pot seedless synthesis. The size and the density of the plates on the surface of Au can be readily tuned with the amount of the thiol ligand, resembling different roughness of the surface. Arising from the different surface roughness, the localized surface plasmon resonance (LSPR) of these shape and morphological alike Au nanoparticles can be continuously tuned within the visible-NIR region. The broad LSPR absorptions and feasible tunability make the Au nanoparticles suitable candidate for plasmonic-related applications. Interestingly, huge SERS enhancement was simultaneously achieved based on the specific surface roughness. Our results demonstrate the great potentials for tuning the LSPR and SERS of Au nanostructures through the engineering of the surface morphologies, which would assist for the design, synthesis, and applications of Au-based plasmonic nanomaterials in various fields. [ABSTRACT FROM AUTHOR]

Cobalt ferrite–silica–gold nanocomposite (CoFe2O4@SiO2@Au) is synthesized using a new method involving: i) the polyol method for cobalt ferrite nanoparticles (CoFe2O4), ii) the Stober method for silica coating, iii) surface functionalization with 3‐aminopropyl triethoxysilane (APTES), and iv) decoration with gold nanoparticles via tetrakis hydroxy‐methyl‐phosphonium (THPC) reduction. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) confirm the morphology of the nanoparticles and coatings for the nanocomposites. Ultraviolet–visible (UV–Vis) absorption spectra exhibit plasmon resonance peaks with tuned shifts, discuss in terms of the difference in dielectric permittivity in the core where gold nanoparticles are anchored. Magnetic hysteresis analysis reveals superparamagnetic behavior with reduced saturation magnetization for the nanocomposites. These findings are useful, as superparamagnetic behavior combined with control of plasmonic emission is highly relevant for several magneto‐plasmonic applications. [ABSTRACT FROM AUTHOR]

Alpha‐synuclein oligomers play a crucial role in the early diagnosis of Parkinson's disease (PD). In this study, a mercaptoundecanoic acid (MUA)‐capped gold nanorod (GNR)‐coated and chitosan (CH)‐immobilized fiber optic probe has shown considerable sensitivity of its detection. The proposed U‐shaped fiber optic biosensor based on localized surface plasmon resonance (LSPR) was applied to detect α‐syn oligomer (OA) biomarker. By analyzing OA concentrations, the biosensor achieved a limit of detection of (LOD) 11 pM within the concentration range of 10–100 pM and the sensitivity value was found as 502.69 Δλ/RIU. Upon analysis of the CV% (coefficient of variation) and accuracy/recovery values, it is revealed that the sensor successfully fulfilled the criteria for success, displaying accuracy/recovery values within the range of 80%–120% and CV% values below 20%. This sensor presents significant advantages, including high sensitivity, specificity, and ability to detect very low concentrations of OA. In conclusion, the suggested U‐shaped fiber optic biosensor has the potential to be valuable in the early detection of PD from a clinical perspective. [ABSTRACT FROM AUTHOR]

In this paper, a three-layer structure of silver particle (AgNP)-dielectric-metal is proposed and constructed based on the characteristics of AgNPs that can excite LSPR (Localized Surface Plasmon Resonance) in free space. In order to overcome the problem of AgNPs easily oxidizing in the air, this paper synthesizes AgNPs using the improved Tollens method and effectively suppresses the coffee-ring effect by changing the solution evaporation conditions, so that the distribution of AgNPs in the deposition area is relatively uniform. The structure proposed in this paper takes advantage of the flexibility of nanoparticle application. The AgNPs deposited on the dielectric layer can effectively localize energy and regulate the LSPR of the device well. The structure can not only achieve precise regulation of the LSPR resonance peak of AgNPs but also can be used as a SERS substrate. [ABSTRACT FROM AUTHOR]

Lead, a prevalent heavy metal, poses significant risks to human health through various exposure pathways. Herein, we propose an extremely sensitive assay toward lead ion (Pb2+) using gold nanorods (GNRs) as probes based on its catalytic activity on etching gold in the presence of 2‐mercaptoethanol and sodium thiosulfate. In the presence of Pb2+, etching predominantly occurs at the two ends of GNRs, leading to the reduction of aspect ratio and the corresponding blueshift of the localized surface plasmon resonance (LSPR). With increasing Pb2+ concentration over the range of 0–50 μM, the color of GNR solution lightens, ultimately becoming colorless. The wavelength shift (Δλ) of LSPR is highly dependent on Pb2+ concentration, with a linear regression equation of Δλ = 10.05ln[Pb2+] + 9.59 and an R2 = 0.995. The assay demonstrates high selectivity for Pb2+ over other potentially interfering ions such as Cu2+ because of its special catalytic activity in the etching of GNRs and the complexing ability of 2‐mercaptoethanol and sodium thiosulfate. Validation of the assay was accomplished by analyzing several forest‐derived food samples, affirming the accuracy in real‐world scenarios. The assay we developed holds promise for many applications in environmental protection and food safety. [ABSTRACT FROM AUTHOR]

Adulteration of expensive vegetable oils with other cheaper vegetable oils is increasing within the oil traders all across the world. Therefore, developing a method for detection of adulteration in expensive vegetable oil like VCO would be useful. In this study, an android mobile application which can generate signature and barcodes has been developed based on the response (p < 0.05) coupled with the optimized condition of LSPR system for different adulterations in VCO with coconut oil (CO) and mustard oil (MO). The discriminant analysis with samples showed a gradual shift to right with the adulteration, demonstrating the independency of the prediction. The correct % of validated samples was observed to be 81.67% and 80% for adulterated sample of VCO with MO and CO respectively with a cumulative variance of 100%. The LOD and LOQ were found to be 0.23 and 0.77 and 0.21 and 0.72 for adulterated samples of VCO with CO and MO respectively with a linearity range of 10 to 90%. The results showed that the technique has a faster response and lower cost than other conventional methods like FT-R or GC–MS/MS for the detection of adulteration in VCO. However, further research is needed for the advancement of android mobile application and to make the system compatible to detect adulteration with other cheap oils. [ABSTRACT FROM AUTHOR]

To date, the advanced synthetic approaches for palladium nanoparticle-based catalysts involve multistep, toxic, and high-cost fabrication routes with low catalytic and sensing performance. In this work, we introduce a new one-shot approach to produce highly sensitive Pd nanocomposites using a large-area polymer self-assembly strategy. This synthesis method allowed us to control the Pd nanoparticle shape and to tailor their plasmonic band positions in a wide light spectral range from ~350 to ~800 nm. We thus determined the critical synthesis conditions that give rise to a ringlike morphology in a reproducible manner. No need for a reducing agent and preliminary functionalization of the surface supporting the nanoparticles upon synthesis. To the best of our knowledge, few works have demonstrated the good performance of PdNPs in sensing. Here, we have demonstrated a robust SERS response for 4-mercaptopyridine with an enhancement factor of 4.2 × 105. We were able to exceed this high value, which matches the current maximum found in the literature, by decreasing the gap distances between Pd nanorings due to the high density of hotspots and the exacerbation of the coupling effect between PdNPs. These tailored products provide new insights for the use of Pd nanomaterials in photocatalysis applications, according to the well-established catalytic performance of Pd materials obtained in this work. [ABSTRACT FROM AUTHOR]

[Display omitted] • Designed a novel multifunctional CuTCPP/MXene/TiO 2 catalyst by crystal plane regulation and hydrogen bonding. • Developed a system for atmospheric CO 2 capture and in-situ conversion at the gas-solid interface. • There is no need to add any sacrificial agent and alkaline absorbent in the reaction system. • The catalyst demonstrated excellent CO 2 conversion rates, effectively producing CO and CH 4. Directly capturing atmospheric CO 2 and converting it into valuable fuel through photothermal synergy is an effective way to mitigate the greenhouse effect. This study developed a gas–solid interface photothermal catalytic system for atmospheric CO 2 reduction, utilizing the innovative photothermal catalyst (Cu porphyrin) CuTCPP/MXene/TiO 2. The catalyst demonstrated a photothermal catalytic performance of 124 μmol·g−1·h−1 for CO and 106 μmol·g−1·h−1 for CH 4 , significantly outperforming individual components. Density functional theory (DFT) results indicate that the enhanced catalytic performance is attributed to the internal electric field between the components, which significantly enhances carrier utilization. The introduction of CuTCPP reduces free energy of the photothermal catalytic reaction. Additionally, the local surface plasmon resonance (LSPR) effect and high-speed electron transfer properties of MXene further boost the catalytic reaction rate. This well-designed catalyst and catalytic system offer a simple method for capturing atmospheric CO 2 and converting it in-situ through photothermal catalysis. [ABSTRACT FROM AUTHOR]

[Display omitted] Localized surface plasmon resonance (LSPR) effect plays a crucial role in the field of solar energy utilization. In this work, we successfully prepared a Cu 2-x Se/ZnSe S-scheme heterojunction with a broad-spectrum response using the hot-injection and low-temperature water bath method. Importantly, we demonstrated that the photothermal effect induced by the LSPR of nonstoichiometric Cu 2-x Se can significantly improve the slow kinetics of water splitting, resulting in an apparent activation energy reduction from 50.1 to 28.7 kJ·mol−1. This improvement is responsible for achieving the highest photocatalytic H 2 evolution rate of 63.6 mmol·g−1·h−1 over 2.7 % Cu 2-x Se/ZnSe under the wavelength ranged from 200 to 2500 nm, which is 3.4 and 5.6 times higher than that of ZnSe and Cu 2-x Se, respectively. Furthermore, the composite exhibits a remarkable H 2 production rate of 0.108 mmol·g−1·h−1 under near-infrared spectroscopy (800<λ<2500 nm), while ZnSe shows limited capability in H 2 releasing. Additionally, Cu 2-x Se/ZnSe demonstrates distinct photocurrent response when λ > 800 nm. The enhanced performance in H 2 evolution can be attributed to the synergistic effect of LSPR-induced light absorption and S-scheme heterojunction, which not only expands the light absorption range to the near-infrared region but also facilitates hot electron injection, charge carrier separation and transfer, leading to a faster surface reaction kinetics. This study provides an effective approach for designing a broad-spectrum light responsive non-precious metal-based photothermal-assisted photocatalytic system. [ABSTRACT FROM AUTHOR]

Abstract Surface-enhanced Raman scattering (SERS) exploits localized surface plasmon resonances in metallic nanostructures to significantly amplify Raman signals and perform ultrasensitive analyses. A critical factor for SERS-based analysis systems is the formation of numerous electromagnetic hot spots within the nanostructures, which represent regions with highly concentrated fields emerging from excited localized surface plasmons. These intense hotspot fields can amplify the Raman signal by several orders of magnitude, facilitating analyte detection at extremely low concentrations and highly sensitive molecular identification at the single-nanoparticle level. In this study, mesoscopic star-shaped gold particles (gold mesostars) were synthesized using a three-step seed-mediated growth approach coupled with the addition of silver ions. Our study confirms the successful synthesis of gold mesostars with numerous sharp tips via the multi-directional growth effect induced by the underpotential deposition of silver adatoms (AgUPD) onto the gold surfaces. The AgUPD process affects the nanocrystal growth kinetics of the noble metal and its morphological evolution, thereby leading to intricate nanostructures with high-index facets and protruding tips or branches. Mesoscopic gold particles with a distinctive star-like morphology featuring multiple sharp projections from the central core were synthesized by exploiting this phenomenon. Sharp tips of the gold mesostars facilitate intense localized electromagnetic fields, which result in strong SERS enhancements at the single-particle level. Electromagnetic fields can be further enhanced by interparticle hot spots in addition to the intraparticle local field enhancements when arranged in multilayered arrays on substrates, rendering these arrays as highly efficient SERS-active substrates with improved sensitivity. Evaluation using Raman-tagged analytes revealed a higher SERS signal intensity compared to that of individual mesostars because of interparticle hot spots enhancements. These substrates enabled analyte detection at a concentration of 10− 9 M, demonstrating their remarkable sensitivity for trace analysis applications.

Abstract Our research focuses on enhancing the broadband absorption capability of organic solar cells (OSCs) by integrating plasmonic nanostructures made of Titanium nitride (TiN). Traditional OSCs face limitations in absorption efficiency due to their thickness, but incorporating plasmonic nanostructures can extend the path length of light within the active material, thereby improving optical efficiency. In our study, we explore the use of refractory plasmonics, a novel type of nanostructure, with TiN as an example of a refractory metal. TiN offers high-quality localized surface plasmon resonance in the visible spectrum and is cost-effective, readily available, and compatible with CMOS technology. We conducted detailed numerical simulations to optimize the design of nanostructured OSCs, considering various shapes and sizes of nanoparticles within the active layer (PM6Y6). Our investigation focused on different TiN plasmonic nanostructures such as nanospheres, nanocubes, and nanocylinders, analyzing their absorption spectra in a polymer environment. We assessed the impact of their incorporation on the absorbed power and short-circuit current (Jsc) of the organic solar cell.

Considering that the plasmonic properties of metallic nanoparticles (NPs) are strongly influenced by their dielectric environment, comprehension and manipulation of this interplay are crucial for the design and optimization of functional plasmonic systems. In this study, the plasmonic behavior of silver nanoparticles encapsulated in diverse copolymer dielectric environments was investigated, focusing on the analysis of the emerging localized surface plasmon resonances (LSPRs) through both experimental and theoretical approaches. Specifically, two series of nanostructured silver ultrathin films were deposited via magnetron sputtering on heated Corning Glass substrates at 330 °C and 420 °C, respectively, resulting in the formation of self-assembled NPs of various sizes and distributions. Subsequently, three different polymeric layers were spin-coated on top of the silver NPs. Optical and structural characterization were carried out by means of UV–Vis spectroscopy and atomic force microscopy, respectively. Rigorous Coupled Wave Analysis (RCWA) was employed to study the LSPRs theoretically. The polymeric environment consistently induced a red shift as well as various alterations in the LSPR amplitude, suggesting the potential tunability of the system.

Oxygen vacancies (OV) in nonmetallic plasmonic photocatalysts can decrease the energy barrier for CO2 reduction, boosting C1 intermediate production for potential C2 formation. However, their susceptibility to oxidation weakens C1 intermediate adsorption. Herein we proposed a "photoelectron injection" strategy to safeguard OV in W18O49 by creating a W18O49/ZIS (W/Z) plasmonic photocatalyst. Moreover, photoelectrons contribute to the local multi‐electron environment of W18O49, enhancing the intrinsic excitation of its hot electrons with extended lifetimes, as confirmed by in situ XPS and femtosecond transient absorption analysis. Density functional theory calculations revealed that W/Z with OV enhances CO2 adsorption, activating *CO production, while reducing the energy barrier for *COH production (0.054 eV) and subsequent *CO−*COH coupling (0.574 eV). Successive hydrogenation revealed that the free energy for *CH2CH2 hydrogenation (0.108 eV) was lower than that for *CH2CH2 desorption for C2H4 production (0.277 eV), favouring C2H6 production. Consequently, W/Z achieves an efficient C2H6 activity of 653.6 μmol g−1 h−1 under visible light, with an exceptionally high selectivity of 90.6 %. This work offers a new strategy for the rational design of plasmonic photocatalysts with high selectivity for C2+ products. [ABSTRACT FROM AUTHOR]

MOFs are known for their absorption properties and widely used for accumulation, filtering, sensorics, photothermal, catalytical and other applications. Their combination with plasmonic metal nanoparticles leads to hybrid structures that profit from the stabilizing effect and high porosity of the MOF as well as the optical and electronic properties of the nanoparticles. The growth of MOFs on plasmonic nanoparticles can be monitored in‐situ using LSPR spectroscopy, simultaneously applying microfluidic reaction conditions for the fabrication of NP@MOF structures. Here, a systematic study is conducted using LSPR spectroscopy for the monitoring of the Layer‐by‐Layer deposition of twelve different MOFs, determining the suitability of LSPR spectroscopy for this purpose. In addition to some well‐investigated materials like HKUST‐1, other MOFs such as MIL‐53, MIL‐88 A and Cu‐BDC are deposited successfully. For some MOFs such as Zn‐Fum, the LSPR experiment indicates that no deposition had taken place. The results are confirmed with AFM, SEM and XPS measurements. This work shows that LSPR spectroscopy is suitable for the in‐situ monitoring of LbL MOF growth and the microfluidic setup is a very promising method for the controlled manufacturing of NP@MOF hybrid structures. Further studies may include the optimization of the synthesis process or the transfer to other materials. [ABSTRACT FROM AUTHOR]

Optimizin the efficient light‐trapping in the photothermal conversion by enhancing localized surface plasmon resonance (LSPR) is crucial in improving light‐heat‐conversion efficiency of Ti3C2Tx MXene. However, its susceptibility to oxidation makes it prone to oxides formation, diminishing its metallic properties and significantly reducing the LSPR effect. This work synthesizes a kind of air‐stable hybrid Ti3C2Tx MXenes by a synergistic densification strategy that incorporates sulfhydryl‐bonding between organic and inorganic parts by reacting Ti3C2Tx MXene with thiocarboxylic acids. The resultant shortening of electron transport pathways, enhanced charge density, and the generation of additional electronic states around the Fermi level collectively contribute to an augmented LSPR effect. Additionally, the hybrid Ti3C2Tx MXenes also demonstrate high‐temperature resistance and reduced water interactions. These combined effects substantially elevate photothermal conversion efficiency through thiocarboxylic acids modification, reaching a photothermal evaporation rate of 1.77 kg m−2 h−1 with 94.56% efficiency in hybrid Ti3C2Tx MXenes. The approach paves the way for the design and development of a three‐in‐one strategy for photothermal conversion. [ABSTRACT FROM AUTHOR]

The application of malathion, an insecticide derived from organophosphates, raises substantial apprehensions over human health in the context of pest management in agricultural produce. The presence of a lack of specialized knowledge and the intricate nature of traditional diagnostic methods have further intensified these symptoms, resulting in significant and persistent damage to the human body. The present study aims to synthesis a gold-nanobipyramids (AuNBPs) for identifying malathion and other organophosphate pollutants, even at exceedingly low levels of detection. The AuNBPs is synthesis by the utilization of the seed-mediated growth (SMG) method. The UV-Vis spectroscopy analysis has identified 2 unique absorption peaks, specifically transverse surface plasmon resonance (t-SPR) occurring between 550 and 600 nm, and longitudinal surface plasmon resonance (l-SPR) occurring within the wavelength range of 750 to 850 nm. Additional analysis of AuNBPs reveals its capacity for notable and distinctive optical resonance, particularly in the visible and near-infrared regions of the electromagnetic spectrum. This characteristic renders AuNBPs very appropriate for the development of localized surface plasmon resonance (LSPR) sensors. The sensitivity experiments conducted on the LSPR sensor based on AuNBPs have shown compelling evidence of its capability to detect malathion and other pollutants in the AuNBPs growth solution across different concentrations. These findings highlight the sensor's potential for efficient residue detection of malathion. This discovery underscores the significant importance of its function in safeguarding food safety and reducing the potential hazards linked to the utilization of malathion and other insecticides based on organophosphates in agricultural practices. [ABSTRACT FROM AUTHOR]

Surface-enhanced Raman scattering (SERS) exploits localized surface plasmon resonances in metallic nanostructures to significantly amplify Raman signals and perform ultrasensitive analyses. A critical factor for SERS-based analysis systems is the formation of numerous electromagnetic hot spots within the nanostructures, which represent regions with highly concentrated fields emerging from excited localized surface plasmons. These intense hotspot fields can amplify the Raman signal by several orders of magnitude, facilitating analyte detection at extremely low concentrations and highly sensitive molecular identification at the single-nanoparticle level. In this study, mesoscopic star-shaped gold particles (gold mesostars) were synthesized using a three-step seed-mediated growth approach coupled with the addition of silver ions. Our study confirms the successful synthesis of gold mesostars with numerous sharp tips via the multi-directional growth effect induced by the underpotential deposition of silver adatoms (AgUPD) onto the gold surfaces. The AgUPD process affects the nanocrystal growth kinetics of the noble metal and its morphological evolution, thereby leading to intricate nanostructures with high-index facets and protruding tips or branches. Mesoscopic gold particles with a distinctive star-like morphology featuring multiple sharp projections from the central core were synthesized by exploiting this phenomenon. Sharp tips of the gold mesostars facilitate intense localized electromagnetic fields, which result in strong SERS enhancements at the single-particle level. Electromagnetic fields can be further enhanced by interparticle hot spots in addition to the intraparticle local field enhancements when arranged in multilayered arrays on substrates, rendering these arrays as highly efficient SERS-active substrates with improved sensitivity. Evaluation using Raman-tagged analytes revealed a higher SERS signal intensity compared to that of individual mesostars because of interparticle hot spots enhancements. These substrates enabled analyte detection at a concentration of 10− 9 M, demonstrating their remarkable sensitivity for trace analysis applications. [ABSTRACT FROM AUTHOR]

Ultraviolet (UV) photodetectors have attracted extensive attention in various applications, including aerospace, optical communication, and fire warning. However, the intrinsic coupling of high responsivity and fast response as well as imperfect interface transmission impede the further improvement of UV photodetector. Here, a high‐performance Au‐decorated PbI2/ZnO pn junction UV photodetector with a one‐dimensional (1D) and two‐dimensional (2D) interspersed structure is presented. The pyro‐phototronic effect and energy band engineering effect from the localized pn junction generated by the layered p‐type PbI2 nanosheets along the c‐axis of ZnO are coupled to modulate the separation and transport of photogenerated carriers. Furthermore, the localized surface plasmon resonance of Au nanoparticles produces transient thermal power to raise temperature fast to enhance pyroelectric current. The self‐powered Au@PbI2/ZnO photodetector displays a high responsivity of 0.21 A W−1, excellent detectivity of 7.9 × 1012 Jones, and fast response/recovery time of 25/31 ms, under the illumination of 325 nm light with the power density of 0.08 µW cm−2. This work offers an effective strategy for designing high‐performance next‐generation optoelectronic devices. [ABSTRACT FROM AUTHOR]

The opto-thermal properties of Au- and Ag-coated core–shell hybrid nanoparticles (NPs) have been thoroughly investigated by using the PyMieLab V1.0 simulation tool based on electrodynamics modelling. We, specifically, investigated the plasmonic resonance tunability and spatial temperature profiles of Au- and Ag-coated composed hybrid core–shell nanospheres as optimized combinations of alloy core (viz. Au0.25Ag0.75, Au0.25Cu0.75, Au0.75Al0.25, Ag0.75Cu0.25 and Ag0.75Al0.25) immersed in the local water (n = 1.33) media. In the present core–shell nanostructure configuration, the alloy core radius (r ) has been changed from 5 to 50 nm (with 5-nm step-size) and shell thickness, t = 5 , and 10 nm is kept the same with varying core radii. The localized surface plasmon resonance (LSPR) of Au- and Ag-coated optimized alloys composed of hybrid core–shell nanospheres is tuned between 238–545 nm and 347–531 nm, respectively, and lies under the ultraviolet–visible segment of the electromagnetic band. The temperature recorded at the surface of core–shell NPs (i.e. alloy core@gold/silver shell) lies between the range of 0.20 and 2.38 °C (for Au-coated alloys) and 0.64–2.44 °C (for Ag-coated alloy) with different core/shell size ratios. The present results are of paramount importance for using these alloy core–plasmonic shell NPs in several types of thermoplasmonic applications. [ABSTRACT FROM AUTHOR]

Ciprofloxacin is a fluoroquinolone group antibiotic used to treat variety of bacterial illnesses. The purpose of this study is to develop a rapid and accurate spectrophotometric approach for the detection of ciprofloxacin using gold nanoparticles (GNPs). Localized surface plasmon resonance (LSPR) absorption band of GNPs at 523.0 nm was utilized as the spectrophotometric detection of ciprofloxacin. To determine the optimum GNPs concentration and pH value of the phosphate buffer solution used in the experimental research, the effect of pH values and GNPs concentrations in the absorbance value of ciprofloxacin-GNPs was investigated. The linear operating range for the developed spectrophotometric method was 0.015–1.48 µg/mL in pH 7.0 phosphate buffer solution. In the recovery study conducted to detect the amount of ciprofloxacin in commercial ear drops, the recovery value was calculated as 91.06 ± 1.21%. [ABSTRACT FROM AUTHOR]

Optical materials with a tunable localized surface plasmon resonance (LSPR) are of great interest for applications in photonics and optoelectronics. In the present study, we explored the potential of generating an LSPR band with an ultra-broad range of over 1000 nm in gold nanoparticles (NPs), precipitated through a thermal treatment in ZnO-Al2O3-SiO2 glass. Using optical absorption spectroscopy, we demonstrated that the LSPR band's position and shape can be finely controlled by varying the thermal treatment route. Comprehensive methods including Raman spectroscopy, X-ray diffraction, and high-resolution transmission electron microscopy were used to study the glass structure, while computational approaches were used for the theoretical description of the absorption spectra. The obtained results allowed us to suggest a scenario responsible for an abnormal LSPR band broadening that includes a possible interparticle plasmonic coupling effect taking place during the liquid–liquid phase separation of the heat-treated glass. The formation of gold NPs with an ultra-broad LSPR band in glasses holds promise for sensitizing rare earth ion luminescence for new photonics devices. [ABSTRACT FROM AUTHOR]

The realization of higher coupling strengths between coupled resonant modes enables exploration of compelling phenomena in diverse fields of physics and chemistry. In this study, we focus on the modal coupling between localized surface plasmon resonance (LSPR) of Au nanoparticles (Au-NPs) and Fabry–Pérot mode (p-NiO/Au film). The effects of nanoparticle size, projected surface coverage (PSC), interparticle distance (IPD), and arrangement to the coupling strength between the two modes are theoretically investigated using finite-difference time-domain (FDTD) method. Au-NPs/p-NiO/Au film (ANA) nanostructures with NPs size of 10 nm, 30 nm, and 50 nm are considered. Numerical calculations point to larger size and higher projected surface coverage (also smaller IPD) of NPs as pre-eminent factors in enhancing the strength of modal coupling. ANA nanostructure with NPs size of 30 nm (ANA-30) and 50 nm (ANA-50) are experimentally fabricated via a facile air–liquid interface self-assembly. The fabricated nanodevices exhibit immense Rabi splitting energies of 655 meV (ANA-30) and 770 meV (ANA-50), and thus fulfill the ultrastrong coupling condition with remarkable splitting energy to bare (plasmon) energy ratio of 0.35 (ANA-30) and 0.4 (ANA-50). The physical insights presented in this study, together with the simple and scalable fabrication process, establish a viable approach to realize stronger coupling between LSPR and Fabry–Pérot mode in metal NPs/dielectric/metal film systems. This will be vital to take advantage of the promising performance enhancements of plasmonic-based nanostructures under strongly coupled regimes in areas such as solar to fuel conversion, sensing, opto-electronics, and quantum applications. [ABSTRACT FROM AUTHOR]

Considering that the plasmonic properties of metallic nanoparticles (NPs) are strongly influenced by their dielectric environment, comprehension and manipulation of this interplay are crucial for the design and optimization of functional plasmonic systems. In this study, the plasmonic behavior of silver nanoparticles encapsulated in diverse copolymer dielectric environments was investigated, focusing on the analysis of the emerging localized surface plasmon resonances (LSPRs) through both experimental and theoretical approaches. Specifically, two series of nanostructured silver ultrathin films were deposited via magnetron sputtering on heated Corning Glass substrates at 330 °C and 420 °C, respectively, resulting in the formation of self-assembled NPs of various sizes and distributions. Subsequently, three different polymeric layers were spin-coated on top of the silver NPs. Optical and structural characterization were carried out by means of UV–Vis spectroscopy and atomic force microscopy, respectively. Rigorous Coupled Wave Analysis (RCWA) was employed to study the LSPRs theoretically. The polymeric environment consistently induced a red shift as well as various alterations in the LSPR amplitude, suggesting the potential tunability of the system. [ABSTRACT FROM AUTHOR]

AbstractThe synthesis of GeO2 NCs and AgNPs/GeO2 NCs is carried out using germanium as starting material and pseudomonas putida in the presence of a low magnetic field for sustainable bacterial growth under oxidation stress and ambient conditions. The galvanic reaction has favored producing Ag NPs on the surface of GeO2 NCs without Ag2O formation. The Ag nanoparticles on the surface of GeO2 NCs will tune their optical properties. AgNPs/GeO2NCs exhibited enhanced PL and Raman intensities with peak shifts due to surface plasmon resonance. Bacterial inhibition will influence the formation of GeO2 nanostructures under oxidation stress. The generated reactive oxygen species during synthesis will form defects in the nanostructures. The defects, excitation wavelength, and Ag concentration will influence the optical properties of GeO2 nanostructures. The improvement in the bacterial culture, temperature regulation, and bacteria–germanium interactions can assist to synthesize optimum GeO2 nanostructures for optoelectronic applications. [ABSTRACT FROM AUTHOR]

The inclusion of nanoparticles in technological development increases every year. For example, metallic nanoparticles are applied in cosmetics, medicine, and sensing areas among others. When light interacts with metallic nanoparticles, the Localized Surface Plasmon Resonance (LSPR) can occur. LSPR is the subject of advanced courses in Physics and some of the students could have several difficulties in its comprehension. To benefit the students, it is proposed a very simple simulator built in Python to study the influence of the features of metallic spherical nanoparticles and of the host medium in the LSPR effect through the Mie Theory.

Indian red scorpion Mesobuthus tamulus is responsible for substantial mortality in India and Sri Lanka; however, no specific diagnostic method is available to detect the venom of this scorpion in envenomed plasma or body fluid. Therefore, we have proposed a novel, simple, and rapid method for detecting M. tamulus venom (MTV) in the plasma of envenomed animals using polyclonal antibodies (PAb) raised against three modified custom peptides representing the antigenic epitopes of K+ (Tamapin) and Na+ (α-neurotoxin) channel toxins, the two major MTV toxins identified by proteomic analysis. The optimum PAb formulation containing PAb 1, 2, and 3 in proportion (1:1:1, w/w/w) acted synergistically, demonstrating significantly higher immunological recognition of MTV than anti-scorpion antivenom (developed against native toxins) and individual antibodies against peptide immunogens. The PAb formulation could detect MTV optimally in envenomed rat plasma (intravenous and subcutaneous routes) at 30–60 min post-injection. The acetonitrile precipitation method developed in this study to augment the MTV detection sensitivity enriched the low molecular mass peptide toxins in envenomed rat plasma, which was ascertained by mass spectrometry analysis. The gold nanoparticles conjugated PAb formulation, characterised by biophysical techniques such as Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM), demonstrated their interaction with low molecular mass MTV peptide toxins in envenomed rat plasma. This interaction results in the accumulation of the gold nanoparticles, thus leading to signal change in absorbance spectra that can be discerned within 10 min. From a standard curve of MTV spiked plasma, the quantity of MTV in envenomed rat plasma could be determined by gold nanoparticle-PAb formulation conjugate.

Abstract Magneto‐plasmonic particles, comprising gold and iron oxide, exhibit substantial potential for biosensing applications due to their distinct properties. Gold nanoparticles (AuNPs) provide plasmonic features, while iron oxide composites, responsive to an external magnetic field, significantly reduce detection time compared to passive diffusion. This study explores core@satellite magneto‐plasmonic particles (CSMPs), featuring magnetic nanoparticle clusters and numerous satellite‐like AuNPs, to amplify the optical response on a nanostructured gold surface. Using a sandwich scheme, target analytes are detected as hybrid nanoparticles bind to the pre‐immobilized target on the AuNPs surface, inducing changes in the immunosensor's extinction spectrum. Application of an external magnetic field notably enhances biosensor response and sensitivity, reducing assay time from hours to minutes. Leveraging the properties of CSMPs, the immunosensor detects specific immune protein at low concentrations within minutes. CSMPs hold considerable promise for precise and sensitive analyte detection, offering potential applications in rapid testing and mass screening.

Optical materials with a tunable localized surface plasmon resonance (LSPR) are of great interest for applications in photonics and optoelectronics. In the present study, we explored the potential of generating an LSPR band with an ultra-broad range of over 1000 nm in gold nanoparticles (NPs), precipitated through a thermal treatment in ZnO-Al2O3-SiO2 glass. Using optical absorption spectroscopy, we demonstrated that the LSPR band’s position and shape can be finely controlled by varying the thermal treatment route. Comprehensive methods including Raman spectroscopy, X-ray diffraction, and high-resolution transmission electron microscopy were used to study the glass structure, while computational approaches were used for the theoretical description of the absorption spectra. The obtained results allowed us to suggest a scenario responsible for an abnormal LSPR band broadening that includes a possible interparticle plasmonic coupling effect taking place during the liquid–liquid phase separation of the heat-treated glass. The formation of gold NPs with an ultra-broad LSPR band in glasses holds promise for sensitizing rare earth ion luminescence for new photonics devices.

A novel photonic crystal fiber (PCF) sensor for refractive index detection based on polydimethylsiloxane (PDMS) is presented in this research, as well as designs for single-channel and dual-channel structures for this PDMS-PCF sensor. The proposed structures can be used to develop sensors with biocompatible polymers. The performance of the single-channel PDMS-PCF sensor was studied, and it was found that adjusting parameters such as pore diameter, lattice constant, distance between the D-shaped structure and the fiber core, and the radius of gold nanoparticles can optimize the sensor's performance. The findings indicate that the detection range of the single-channel photonic crystal is 1.21–1.27. The maximum wavelength sensitivity is 10,000 nm/RIU with a resolution of 1 × 10 − 5 RIU, which is gained when the refractive index is set to 1.27. Based on the results of the single-channel PCF, a dual-channel PDMS-PCF sensor is designed. The refractive index detection range of the proposed sensor is 1.2–1.28. The proposed sensor has a maximum wavelength sensitivity of 13,000 nm/RIU and a maximum resolution of 7.69 × 10 − 6 RIU at a refractive index of 1.28. The designed PDMS-PCF holds tremendous potential for applications in the analysis and detection of substances in the human body in the future. [ABSTRACT FROM AUTHOR]

The utilization of plasmonic nanomaterials in catalytic technologies is an emerging research field with foreseeable applications in energy-catalytic technologies. On this front, the coupling of plasmonic nanomaterials with molecular catalysts is a newly approached, thus far unexploited field, that we discuss herein. In the present mini review, we contrast the case where the plasmonic particle itself is the catalytic center against the case where the plasmonic particle acts as a co-catalyst for an operational catalytic system. In the first part, we present an outline of the key phenomena in nanoplasmonics, and their potential implications in catalytic processes. The concepts of hot electrons, hot holes, and the dynamics of their generation and transfer are reviewed, as are the contribution of near-field and photothermal effects to catalytic processes. All these plasmonic-phenomena are then discussed in conjunction with representative catalytic systems from the literature. [ABSTRACT FROM AUTHOR]

The increasing demand for rapid, cost-effective, and reliable diagnostic tools in personalized and point-of-care medicine is driving scientists to enhance existing technology platforms and develop new methods for detecting and measuring clinically significant biomarkers. Humanity is confronted with growing risks from emerging and recurring infectious diseases, including the influenza virus, dengue virus (DENV), human immunodeficiency virus (HIV), Ebola virus, tuberculosis, cholera, and, most notably, SARS coronavirus-2 (SARS-CoV-2; COVID-19), among others. Timely diagnosis of infections and effective disease control have always been of paramount importance. Plasmonic-based biosensing holds the potential to address the threat posed by infectious diseases by enabling prompt disease monitoring. In recent years, numerous plasmonic platforms have risen to the challenge of offering on-site strategies to complement traditional diagnostic methods like polymerase chain reaction (PCR) and enzyme-linked immunosorbent assays (ELISA). Disease detection can be accomplished through the utilization of diverse plasmonic phenomena, such as propagating surface plasmon resonance (SPR), localized SPR (LSPR), surface-enhanced Raman scattering (SERS), surface-enhanced fluorescence (SEF), surface-enhanced infrared absorption spectroscopy, and plasmonic fluorescence sensors. This review focuses on diagnostic methods employing plasmonic fluorescence sensors, highlighting their pivotal role in swift disease detection with remarkable sensitivity. It underscores the necessity for continued research to expand the scope and capabilities of plasmonic fluorescence sensors in the field of diagnostics. [ABSTRACT FROM AUTHOR]

The issue of water pollution has emerged as a formidable challenge, prompting a pressing need for solutions. The utilization of metal nanoparticles with surface plasmon resonance and semiconductor composite photocatalysts is regarded as a highly effective approach to solve this problem. g-C3N4 is an effective catalyst for the degradation of organic pollutants. Its photocatalytic performance is usually enhanced by the use of the noble metal Au Ag. However, the high cost of these materials limits their application. In this study, we present the synthesis of Al NPs/g-C3N4 nanocomposites using the bridging effect of ligands. The characterized of transmission electron microscopy (TEM), X-ray diffractometer (XRD) and ultraviolet-visible spectroscopy (UV-Vis) proved that Al NPs/g-C3N4 with a wider light absorption range were successfully synthesized. The effects of ligands, (glutathione (GSH), glutamic acid (GAG), and cysteine (CYS)), Al diameter (40 to 200 nm) and the ratio of Al to g-C3N4 (1:1 to 5:1) on the photocatalytic degradation of methylene blue (MB) by Al NPs/g-C3N4 were also evaluated. The results showed that the optimum degradation efficiency of Al NPs/g-C3N4 for MB at 5 mg/L reached 100% within 60 min, which was 11 times higher than that of pure g-C3N4. The principal analysis of Al enhancing the photocatalytic performance of g-C3N4 was studied through transient photocurrent spectroscopy (TPC), electrochemical impedance spectroscopy (EIS), and steady-state transient fluorescence spectroscopy (PL). The results confirmed that hot carriers generated by localized surface plasmon resonance (LSPR) of Al nanoparticles increase the carrier concentration. In addition, the Schottky barrier generated by Al and g-C3N4 could also improve the carrier separation rate and increase the carrier lifetime. This work is expected to solve the problem of organic wastewater treatment and lay the foundation for subsequent research on photocatalysis. [ABSTRACT FROM AUTHOR]

Ultrasensitive and rapid detection of single extracellular vesicles (EV) in complex biological samples requires a biosensor that possesses remarkable specificity, cost‐effectiveness, and ease of use; however, this remains a big challenge owing to the small size and high heterogeneity of EV in samples. Although reported biosensors can detect biomarkers in complex biological samples, tedious preprocessing procedures, low sensitivity, and expensive and complicated production hinder their use in early‐stage cancer diagnostics. To address these issues, an optical microfiber modified with WS2‐supported gold nanobipyramid (Au NBPs) nanointerfaces for the ultrasensitive assay of prostate cancer (PC) exosomes is proposed. Owing to the strong localized surface plasmon resonance (LSPR) hotspots of the Au NBPs coupled with the WS2 nanointerface, the sensor could ultrasensitively detect exosomes with an ultralow limit of detection (LODs) of 23.5 particles mL−1 in phosphate‐buffered saline (PBS) solution and 570.6 particles mL−1 in 10% serum. The LOD of 23.5 particles mL−1 is two orders of magnitude lower than those reported for other cutting‐edge techniques. Based on this sensing scheme, the sensor can distinguish PC serum from healthy serum, and successfully diagnose patients' whole blood by capturing and sizing a single bioparticle. This work presents a novel method for analyzing whole blood with ultrahigh sensitivity. [ABSTRACT FROM AUTHOR]

Solar-driven photocatalytic CO2 conversion is a promising strategy to alleviate the energy crisis and reduce the level of CO2 emissions. In this study, GaN@β-Ga2O3 core–shell nanowire (NW) arrays were prepared via the thermal oxidation of GaN NWs, and their photocatalytic CO2 reduction performance was investigated. GaN@β-Ga2O3 NWs exhibited superior photocatalytic activity compared to GaN NWs and β-Ga2O3 NWs under simulated sunlight irradiation. The average CO production rate reached ∼447.30 μmol g–1 h–1 within 3 h. The photocatalytic reduction process was further enhanced using GaN@β-Ga2O3 NWs with Ag nanoparticles of ∼18 nm size as cocatalysts, and its average rate increased to ∼689.18 μmol g–1 h–1. The ternary heterostructured photocatalyst demonstrated excellent synergistic effects and high efficiency in environmental protection and energy conversion applications. [ABSTRACT FROM AUTHOR]

Plasmonic heterostructures refer to the class of hybrid nanostructures where two or more nanocrystals (NCs) are chemically bonded, at least one of which is plasmonic. The light concentration property of plasmons is used to manipulate the light–matter interaction in the resulting heterostructures for applications in the fields of nanoscience, photonics, catalysis, and biology among many others. With the advancement of colloidal synthesis, plasmonic heterostructures have a versatile landscape of their own in the last couple of decades. In particular, after the discovery of semiconductor plasmonic NCs (In2O3, CdO, Cu2–xS, etc.) and halide perovskite NCs (CsPbX3, X: Cl, Br, I), the possibility of heterostructures expanded multifold. Nevertheless, challenges remain in successfully synthesizing phase pure structures, optimizing the right geometry and composition for applications, or more fundamentally, observing plasmonic properties despite the formation of heterostructures. In this Review, we briefly review the progress of the colloidal plasmonic heterostructures in terms of synthesis, optical properties, and applications. We discuss these aspects in the traditional noble metal nanoparticle-based compounds, followed by semiconductor plasmonic and halide perovskite heterostructures. We specifically focus on the current challenges faced by the research community in the field of plasmonic halide perovskites and how fundamental design principles can bypass the current limitations. [ABSTRACT FROM AUTHOR]

This study explores the potential of laser-induced nano-photon-poration as a non-invasive technique for the intracellular delivery of micro/macromolecules at the single-cell level. This research proposes the utilization of gold-coated spiky polymeric nanoparticles (Au-PNPs) and gold nanorods (GNRs) to achieve efficient intracellular micro/macromolecule delivery at the single-cell level. By shifting the operating wavelength towards the near-infrared (NIR) range, the intracellular delivery efficiency and viability of Au-PNP-mediated photon-poration are compared to those using GNR-mediated intracellular delivery. Employing Au-PNPs as mediators in conjunction with nanosecond-pulsed lasers, a highly efficient intracellular delivery, while preserving high cell viability, is demonstrated. Laser pulses directed at Au-PNPs generate over a hundred hot spots per particle through plasmon resonance, facilitating the formation of photothermal vapor nanobubbles (PVNBs). These PVNBs create transient pores, enabling the gentle transfer of cargo from the extracellular to the intracellular milieu, without inducing deleterious effects in the cells. The optimization of wavelengths in the NIR region, coupled with low laser fluence (27 mJ/cm2) and nanoparticle concentrations (34 µg/mL), achieves outstanding delivery efficiencies (96%) and maintains high cell viability (up to 99%) across the various cell types, including cancer and neuronal cells. Importantly, sustained high cell viability (90–95%) is observed even 48 h post laser exposure. This innovative development holds considerable promise for diverse applications, encompassing drug delivery, gene therapy, and regenerative medicine. This study underscores the efficiency and versatility of the proposed technique, positioning it as a valuable tool for advancing intracellular delivery strategies in biomedical applications. [ABSTRACT FROM AUTHOR]

The heightened transmissibility and capacity of African swine fever virus (ASFV) induce fatal diseases in domestic pigs and wild boars, posing significant economic repercussions and global threats. Despite extensive research efforts, the development of potent vaccines or treatments for ASFV remains a persistent challenge. Recently, inhibiting the AsfvPolX, a key DNA repair enzyme, emerges as a feasible strategy to disrupt viral replication and control ASFV infections. In this study, a comprehensive approach involving pharmacophore-based inhibitor screening, coupled with biochemical and biophysical analyses, were implemented to identify, characterize, and validate potential inhibitors targeting AsfvPolX. The constructed pharmacophore model, Phar-PolX-S, demonstrated efficacy in identifying a potent inhibitor, D-132 (IC50 = 2.8 ± 0.2 µM), disrupting the formation of the AsfvPolX-DNA complex. Notably, D-132 exhibited strong binding to AsfvPolX (KD = 6.9 ± 2.2 µM) through a slow-on-fast-off binding mechanism. Employing molecular modeling, it was elucidated that D-132 predominantly binds in-between the palm and finger domains of AsfvPolX, with crucial residues (R42, N48, Q98, E100, F102, and F116) identified as hotspots for structure-based inhibitor optimization. Distinctively characterized by a 1,2,5,6-tetrathiocane with modifications at the 3 and 8 positions involving ethanesulfonates, D-132 holds considerable promise as a lead compound for the development of innovative agents to combat ASFV infections.

A quick one-step fabrication of efficient SERS substrates by a modified approach based on a silver-mirror reaction (using Tollens’ reagent) is reported. Commercially available microscope slides or cover glass (coverslips) were used as-received, without special surface treatment. In contrast to the commonly used two-step process, the composition of the Tollens reagent was modified to use a single-step process. The obtained rather homogeneous films of densely packed nanoislands are promising for application as substrates for Surface-Enhanced Raman Scattering (SERS), as demonstrated by several different kinds of molecules as analytes. In particular, the achieved level of detection of a standard dye analyte, down to 10-14 M of Rhodamine 6G, is in the range of best values reported in the literature. Low concentrations of some biomolecules are also detected, such as lysozyme (10-4 M), adenine (10-4 M), and salicylic acid (10-5 M). For some analytes, stronger SERS was observed in the drop, and for others after the solvent was dried. The possible reasons for this effect are described. By applying thermal annealing in the inert gas atmosphere, the Ag film morphology can be partially converted into a coral-like 3D structure that may be advantageous for the localization of the analyte in the “hot spots” and allow additional spectral tunability of the plasmon resonance.

The utilization of plasmonic nanomaterials in catalytic technologies is an emerging research field with foreseeable applications in energy-catalytic technologies. On this front, the coupling of plasmonic nanomaterials with molecular catalysts is a newly approached, thus far unexploited field, that we discuss herein. In the present mini review, we contrast the case where the plasmonic particle itself is the catalytic center against the case where the plasmonic particle acts as a co-catalyst for an operational catalytic system. In the first part, we present an outline of the key phenomena in nanoplasmonics, and their potential implications in catalytic processes. The concepts of hot electrons, hot holes, and the dynamics of their generation and transfer are reviewed, as are the contribution of near-field and photothermal effects to catalytic processes. All these plasmonic-phenomena are then discussed in conjunction with representative catalytic systems from the literature.

In this paper, a three-layer structure of silver particle (AgNP)-dielectric-metal is proposed and constructed based on the characteristics of AgNPs that can excite LSPR (Localized Surface Plasmon Resonance) in free space. In order to overcome the problem of AgNPs easily oxidizing in the air, this paper synthesizes AgNPs using the improved Tollens method and effectively suppresses the coffee-ring effect by changing the solution evaporation conditions, so that the distribution of AgNPs in the deposition area is relatively uniform. The structure proposed in this paper takes advantage of the flexibility of nanoparticle application. The AgNPs deposited on the dielectric layer can effectively localize energy and regulate the LSPR of the device well. The structure can not only achieve precise regulation of the LSPR resonance peak of AgNPs but also can be used as a SERS substrate.

In this study, the localized surface plasmon resonances (LSPRs) of Ag nanoparticles (NPs) embedded in ZnO dielectric matrices were studied. Initially, continuous Ag thin films were deposited on Corning glass substrates via magnetron sputtering, followed by post annealing, resulting in the formation of self-assembled nanoparticles. In some cases, a heated substrate holder was employed to induce NP formation during the deposition. The morphology of nanoparticles was studied using atomic force microscopy (AFM). Ultraviolet–visible spectroscopy (UV-Vis) probed the LSPRs. Subsequently, a 70 nm thick ZnO layer was deposited on top of the Ag thin films. For the Ag films, LSPR characteristics were found to depend on the initial film thickness. The ZnO capping layer induced an intense red shift, suggesting its potential as a mechanism for tailoring LSPRs. Lastly, theoretical calculations with the rigorous coupled-wave analysis (RCWA) method were carried out for comparison with the experimental results. [ABSTRACT FROM AUTHOR]

Gallic acid (GA) is known for its valuable properties as an antioxidant, anti-cancer, and anti-mutagenic compound, making its detection in foods and drugs of paramount importance. In this research, we introduce a novel multichromatic sensor for GA detection, which employs the controlled growth of silver nanoparticles (AgNPs) on the surface of gold nanobipyramids (AuNBPs). The sensor exploits GA's capability to reduce AgNO3, resulting in the growth of AgNPs and a subsequent blue shift of localized surface plasmon resonance (LSPR) as large as 195 nm. This unique multicolor response ranges from light gray to green, blue–violet, and pink, allowing for distinctive visual identification of GA concentrations. The sensor's performance demonstrates a wide dynamic range of 0–175 μM, and a detection limit (LOD) as low as 0.139 μM. Notably, the applicability of this multichromic plasmonic probe was successfully tested for GA assay in both Black and Green tea, showcasing highly satisfactory recovery efficiencies and affirming its potential for food quality control applications. The presented multichromatic sensor offers a promising approach for rapid and sensitive GA detection in various food and pharmaceutical products, enhancing the monitoring and assessment of GA content for improved product quality and safety. [ABSTRACT FROM AUTHOR]

We have prepared CoNPs@CN that cobalt nanoparticles(CoNPs) dispersed uniformly in the carbon matrix Composite (CN) via a facile and controllable method. Samples were characterized by X-ray diffraction (XRD), UV–V spectroscopy, scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS). CoNPs@CN exhibited favorable photocatalytic activity under visible light irradiation. The results of quenching and photoluminescence experiments reveal the generation of main active species (•OH and •O 2 − radicals). The producing mechanism of active species can be attributed to that CoNPs@CN absorb photons and generate photogenerated electrons through localized surface plasmon resonance (LSPR) effect, then H2O and O2 in the solution react with the photogenerated hole and electrons to produce •OH and •O 2 − radicals. In the current study, CoNPs@CN are prepared that the cobalt (Co) nanoparticles dispersed uniformly in the carbon matrix via a facile and controllable method. Co@CN exhibited favorable photocatalytic activity under visible light irradiation. Co@CN can absorb photons under illumination through LSPR effect, thus the photogenerated electrons and holes were generated. H2O and O2 in the solution reacted with the photogenerated electrons to produce •OH and •O2– radicals. These two main radicals are used to decompose MO effectively. [ABSTRACT FROM AUTHOR]

Freshwater resources can be sustainably harvested through interfacial evaporation by solar energy. To enhance the efficiency of solar interfacial evaporation, a metal–graphene alcohol gel is synthesized using a one‐step thermal reduction technique. Subsequently, a metal–graphene aerogel (GA) is produced using freeze‐drying technology. The hydrothermal treatment method is applied to introduce asymmetric moisture and roughness on the upper and lower surfaces of the aerogel. The unique structure of the aerogel plays a significant role in facilitating continuous water transport to the interface for evaporation. The top layer, being hydrophobic, and the bottom layer, being hydrophilic, contribute to this process. Importantly, the top layer's design ensures that an excessively thick water film does not form, thereby preventing any adverse effects on light‐absorption efficiency. The aerogel exhibits that an outstanding water‐evaporation rate is 1.75 kg m−2 h−1 and a remarkable photothermal conversion efficiency (PTCE) is 93.17% under one solar radiation intensity. This is because the aerogel has a unique 3D structure. This special 3D structure has an interconnected microporous‐like appearance inside, which increases the evaporation area. Metal–GA is based on the electric field dielectric evaporation mechanism of metal nanoparticles localized surface plasmon resonance effect and the thermal mediated evaporation mechanism of graphene full spectrum. Under the double action, the PTCE is significantly improved. The meticulously created metallic GA performs exceptionally well at evaporating water. As a result, it presents a promising and practical avenue for exploring effective solar interfacial evaporation. [ABSTRACT FROM AUTHOR]

Abstract Urine Specific Gravity (USG) is a direct indicator of the osmolarity of the urine and therefore it can be considered as a nonspecific marker of several underlying diseases which result in changes in hydration levels of the body. Here, a biosensor based on the principle of localized surface plasmon resonance (LSPR) is developed, which utilizes its refractive index sensing properties to measure USG with a sensitivity of 79.21 nm USG−1unit. Additionally, the sensor can measure the serum protein content within the urine. Traditionally, handheld refractometers are used to measure USG which are operated as calibrated refractive index scales rather than a sensor. A simple experiment demonstrating the advantage of a sensor over scale, with LSPR as the transduction method, is also conducted to highlight the enhanced sensitivity of a sensor over a scale. Finally, analysis of results with an unsupervised machine learning algorithm, principal component analysis (PCA), demonstrate the feasibility of automating or perhaps adding artificial intelligence to such sensors, thereby exemplifying a potential paradigm shift from refractive index scales to sensors in USG measurement.

Gold nanoparticles film as a part of an optical sensor is considered as active support in the development of specific chemical or biological biosensors optically. Well-organized gold nanoparticles can be prepared through inexpensive approaches where gold nanoparticles are easily obtained on a glass substrate. Herein, the authors propose a low-cost thermal synthesis of active plasmonic nanostructures on thin gold layers modified by a short annealing time (1 min and 15 min) at 550 °C and quickly followed by simple quenching. The results proved a good reproducibility of localized surface plasmon resonance (LSPR) optical responses with investigate the effects of modified thermal treatment on the morphology of gold thin films, the extinction LSPR spectra characteristics in the range between 350−1000 nm, and the quality factor (Q-factor) of the plasmonic resonance. The present findings that the proposed method gives evidence enhancement with the enrichment factor (EF-factor) values by about 310 %–460 %. We believe our study may have provided a strategy to enhance the fabrication of gold nanoparticles film based on plasmonic nanostructures for LSPR chip sensor applications.