Plasmon Band Research Articles

Optical N-plasmon: topological hydrodynamic excitations in graphene from repulsive Hall viscosity

Edge states occurring in Chern and quantum spin-Hall phases are signatures of the topological electronic band structure in two-dimensional (2D) materials. Recently, a new topological electromagnetic phase of graphene characterized by the optical N-invariant was proposed. Optical N-invariant arises from repulsive Hall viscosity in hydrodynamic many-body electron systems, distinct from the Chern and Z 2 invariants. In this paper, we introduce the topologically protected edge excitation—optical N-plasmon of interacting many-body electron systems in the topological optical N-phase. These optical N-plasmons are signatures of the topological plasmonic band structure in 2D materials. We demonstrate that optical N-plasmons exhibit unique dispersion relations, stability against various boundary conditions, and edge profiles when compared with the topologically trivial edge magneto plasmons. Based on the optical N-plasmon, we design an ultra sub-wavelength broadband topological hydrodynamic circulator, which is a chiral quantum radio-frequency circuit component crucial for information routing and interfacing quantum–classical computing systems. Furthermore, we reveal that optical N-plasmons can be effectively tuned by the neighboring dielectric environment without breaking the topological properties. Our work provides a smoking gun signature of topological electromagnetic phases occurring in 2D materials arising from repulsive Hall viscosity.

Coupling and thermosplasmonic properties of asymmetric hexagonal nanoframes

The interaction of light with asymmetric nanostructures leads to the coupling of plasmon modes. Understanding the nature and tunability of these hybridized plasmon modes is essential for both fundamental studies and the development of new applications. Herein, we systematically examine these coupled plasmon modes and heat generated by the asymmetric hexagonal nanoframes dimers (HNDs). Our results show that there are three plasmon bands in the examined wavelength. One of these bands is related to the coupled plasmon modes, which can be actively controlled by changing the height of nanoparticles. These coupled plasmon modes originate from the interaction of dipoles with a minimum splitting energy of 170 meV. Moreover, the thermoplasmonic studies show that the temperature of the asymmetric HNDs strongly depends on the coupling of nanoframes which shows great promise for highly sensitive thermal imaging.

The Optical and Structural Properties of the Fe@Au Core–Shell Nanoparticles Prepared by PLAL

In this research, metal targets dipped in 3 mL of distilled water (DW) were subjected to pulsed laser ablation. Colloidal dispersions of Fe and Au, and bimetallic Fe@Au core/shell nanoparticles are created. The core/shell structure of these particles was subsequently studied using X-ray diffraction. UV–Vis and HRTEM measurements are used to determine surface Plasmon resonance (SPR) and particle sizes. We also carried out an investigation to gauge the stability in terms of the surface charge of the produced nanoparticles (Zeta-potential). The findings show that maximum absorption value of Fe Nps was 0.45 in the range (200–350) nm, while Au exhibits a surface Plasmon resonance (SPR) peaked at a wavelength of 545 nm in the range (290–1100) nm. Another peak was noticed at (555) nm for the surface Plasmon band of the particles Fe@Au in the range (290–1100) nm, HRTEM measurement was used to check the shape and particle size, and the results showed that the average particle size was less than 50 nm.

The Optimizing of Prefabricated Solar Cells by Dual Plasmonic Nanoparticles

Background: The quest for improving the efficiency of solar cells has garnered considerable attention in numerous scientific investigations. One promising approach involves utilizing plasmons generated by metal nanoparticles to enhance the performance of photovoltaic solar cells.
 Materials and Methods: High-purity gold nanoparticles (AuNPs), silver nanoparticles (AgNPs), and a combination of both were synthesized using pulsed laser ablation in distilled water. Subsequently, these nanoparticles were deposited onto silicon (Si) substrates and pre-existing Si homo-junction photovoltaic cells.
 Results: The optical analysis of the prepared nanoparticle suspension revealed distinct plasmonic bands located at approximately 400 nm and 523 nm wavelengths for AgNPs and AuNPs, respectively. In the case of the AuNPs:AgNPs mixture, two plasmonic bands were observed, corresponding to the presence of both types of metal nanoparticles. The X-ray diffraction (XRD) analysis of the deposited nanoparticle samples on Si wafers demonstrated a polycrystalline structure for all samples. Scanning electron microscopy (SEM) imaging displayed uniformly distributed spherical Au nanoparticles on the substrate, while AgNPs exhibited some aggregations.
 Conclusion: The photovoltaic (PV) solar cells demonstrated an enhanced performance, attributed to the ability of the plasmonic nanoparticles to facilitate increased light absorption or enhance surface conductivity. The combination of silver and gold particles holds promise for solar surface coating, further optimizing the cells to capture a greater amount of solar radiation within their plasmon peaks. This study highlights the potential of plasmonic nanoparticles to enhance the efficiency of previously prepared PV cells.

Green synthesis of copper oxide nanoparticles and its efficiency in degradation of rifampicin antibiotic

In recent ages, green nanotechnology has gained attraction in the synthesis of metallic nanoparticles due to their cost-effectiveness, simple preparation steps, and environmentally-friendly. In the present study, copper oxide nanoparticles (CuO NPs) were prepared using Parthenium hysterophorus whole plant aqueous extract as a reducing, stabilizing, and capping agent. The CuO NPs were characterized via UV–Vis Spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), powder X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), and Dynamic Light Scattering (DLS). The UV–Vis spectra of CuO NPs showed a surface plasmonic resonance band to occur at 340 nm. FTIR analysis revealed the presence of secondary metabolites on the surface of CuO NPs, with a characteristic Cu–O stretching band being identified at 522 cm−1. Scanning electron micrographs and transmission electron micrographs showed that CuO NPs were nearly spherical, with an average particle of 59.99 nm obtained from the SEM micrograph. The monoclinic crystalline structure of CuO NPs was confirmed using XRD, and crystallite size calculated using the Scherrer-Debye equation was found to be 31.58 nm. DLS showed the presence of nanoparticle agglomeration, which revealed uniformity of the CuO NPs. Furthermore, the degradation ability of biosynthesized nanoparticles was investigated against rifampicin antibiotic. The results showed that the optimum degradation efficiency of rifampicin at 98.43% was obtained at 65℃ temperature, 50 mg dosage of CuO NPs, 10 mg/L concentration of rifampicin solution, and rifampicin solution at pH 2 in 8 min. From this study, it can be concluded that CuO NPs synthesized from Parthenium hysterophorus aqueous extract are promising in the remediation of environmental pollution from antibiotics. In this light, the study reports that Parthenium hysterophorus-mediated green synthesis of CuO NPs can effectively address environmental pollution in cost-effective, eco-friendly, and sustainable ways.

Engineering Surface-Enhanced Raman Scattering Probe for Enhanced Detection of Acute Diseases with Paper Microfluidics

Effective and fast detection of acute diseases is still a main challenge for early diagnosis and monitoring treatment. In this work, surface-enhanced Raman scattering (SERS) probes are incorporated into a microfluidic paper strip for antigen biomarker detection. First, a new material is designed to tune plasmon band position and intensity. Second, geometry is optimized to maximize the SERS enhancement factor. The Finite-Difference Time-Domain simulation has confirmed that more hotspots are generated by the above optimization. As a results, the paper microfluidic strip has achieved the limit of detection at pg/mL level toward antigen detection in blood plasma. The paper microfluidic device shows a great potential in early detection of acute diseases at home, clinics, and remote areas with limited resources.

Template-Free Synthesized Gold Nanobowls Composed with Graphene Oxide for Ultrasensitive SERS Platforms.

Engineering of plasmonic properties of gold nanostructures expands the field of their applications from photocatalysis and photothermal effects to ultrasensitive surface-enhanced Raman spectroscopy (SERS). The known methods of preparation of gold nanobowls involve the deposition of gold layer on polymers or silicon nanotemplates and the removal of the top layer of gold together with the template. Such gold nanobowls are characterized by very broad plasmonic bands due to the plasmon hybridization. The sharp edges on the top of nanobowls are potential sources of the strong electromagnetic field beneficial for SERS. We present a novel template-free synthesis of gold nanobowls (AuNBs). The AuNB layers are deposited on graphene oxide (GO) layers. We compare AuNBs with gold nanospheres (AuNSs) and gold nanourchins (AuNUs) having similar size. The gold nanoparticles are combined with pristine GO or graphene oxide conditioned in ammonia (GONH3) or graphene oxide conditioned in sodium hydroxide (GONaOH). The SERS properties of the hybrid supports were studied using rhodamine 6G (R6G) as the SERS probe. The 633 nm laser line was used, which falls out of the molecular resonance with R6G. The results indicate that AuNBs show largely higher enhancement factors when compared to AuNUs and AuNSs. Furthermore, the GO materials are able to modify the SERS enhancement by 1 order of magnitude. We explain the influence of the GO material by three factors: (1) enabling or disabling the charge transfer between gold and R6G, which is crucial for the chemical part of SERS enhancement; (2) causing the aggregation of gold nanoparticles and formation of hot spots; (3) dipole contribution to the electromagnetic enhancement through the abundance of polar groups on the surface.

Photodestruction Action Spectroscopy of Silver Cluster Anions, AgN- (N = 3-19), with a Linear Ion Trap: Observation of Bound Excited States above the Photodetachment Threshold.

Electron detachment thresholds of metal cluster anions, MN-, are a few electron volts. The excess electron is therefore detached by visible or ultraviolet light, which also creates low-lying bound electronic states, MN-*; i.e., MN-* energetically overlaps with the continuum, MN + e-. Here, we perform action spectroscopy of photodestruction, leading either to photodetachment or to photofragmentation, for size-selected silver cluster anions, AgN- (N = 3-19), to unveil such bound electronic states embedded in the continuum. The experiment takes advantage of a linear ion trap that enables us to measure photodestruction spectra with high quality at well-defined temperatures, where bound excited states, AgN-*, are clearly identified above their vertical detachment energies. Structural optimization of AgN- (N = 3-19) is conducted by using density functional theory (DFT), which is followed by calculations of vertical excitation energies by time-dependent DFT to assign the observed bound states. Spectral evolution observed as a function of cluster size is also discussed, where the optimized geometries are found to be closely related to the observed spectral profiles. A plasmonic band consisting of nearly degenerate individual excitations is observed for N = 19.

Modified anode/semiconductor interface by multiple plasmonic resonance bands:Experimental and simulation study

For highly efficient photovoltaic, all the photo-generated carriers should be collected at the electrode. Before reaching the electrode these photo-generated charge carrier undergoes various loss mechanisms. These types of losses have a direct consequence on the PV efficiency. To reduce such losses transport path should be low resistive and trap free. This can be achieved by maintaining the balanced electron and hole mobility of active layer, high conducting transport layers, and making the ideal Schottky and Ohmic contact. In this work, dual and triple nanoparticles were embedded in PEDOT:PSS and the effect of nanoparticle on PV performance is investigated. Metal nanoparticle in the HTL manipulate optoelectronic properties. This work provides some insight in the organic photovoltaics while using metal nanoparticle in the HTL. Primary factor for the enhancement in the efficiency is due to the plasmonic behavior and the improved conductivity of HTL. Obtained result indicates that device with triple nanoparticle HTL showed high PCE than dual nanoparticle and neat devices. Further, the experimental PV results were compared with the simulation results. Results suggest that metal nanoparticle in HTL primarily enhances the short circuit current density and fill factor.

Concept of a Crossed Czerny–Turner Spectrometer With an Integrated Automatic Sampling System for Biodetection Using Ultrastable Gold Nanoparticles

This work presents the design and implementation of a portable optofluidic system for biodetection based on ultrastable gold nanoparticles functionalized with a dopamine binding aptamer. The automatic sampling and mixing fluidic system integrated into a spectrometer is configured to measure the gold nanoparticles’ plasmon band position. The novel molecule detection method based on ultrastable gold nanoparticles has been previously tested using dopamine as the target molecule. The optofluidic system designed for automatic bathochromic shift detection has an optical resolution of 1nm using a 50 μm input slit. The proposed system, compared to other existing molecules detection techniques, has several advantages including portability and automatic detection for <italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">in situ</i> applications.

Silver nanoparticles coated by Schiff base as an adsorbent of lead from polluted water.

Synthesis of silver nanoparticles coated with Schiff base was achieved . Silver nanoparticles are reduced and coated using Schiff base. Schiff base serves as a capping to stop silver oxide from overgrowing. Schiff base produces silver nanoparticles with a novel form and a distinctive appearance. The presence of Schiff base as a reducing and capping agent can give a new shape for prepared silver nanoparticles. The structure of Schiff base was analyzed based on spectral data (1 H nuclear magnetic resonance (H1NMR), Mass spectroscopy, and Fourier-transform infrared spectroscopy (FTIR). The formation of silver nanoparticles within a surface plasmon band at 461 nm was observed using UV-Vis Spectroscopy. Silver nanoparticles with a spherical shape and a particle size between 50 and 100 nm are visible in a scanning electron microscope image. For the first time, silver nanoparticles coated with Schiff base were used to adsorb lead from a sample of polluted water. The rate of adsorption was 69%.

Theory of plasmon-polaritons in binary metallic supercrystals

We present a theory of optical excitations in binary plasmonic supercrystals that are made out of two types of metal nanoparticles. Compared to monodisperse supercrystals, binary crystals have a larger number of plasmonic bands. Their dispersion is governed by the lattice symmetry, unit cell parameters, and shape and material composition of the nanoparticle building blocks. We develop a quantum description of the plasmon polaritons in supercrystals that starts from the dipole and quadrupole excitations of the nanoparticles, their interaction, and their coupling to photons. We show how to use group theory to analyze the plasmon- and photon-induced supercrystal states and their interaction. Plasmon-polaritons of binary metallic supercrystals are in the regime of ultrastrong and deep strong light-matter interaction; i.e., the coupling strength is on the same order as the photon energy. One consequence of the strong interaction is that quadrupolar plasmon modes and photons with energies well above the plasmon energies have to be taken into account to calculate the polariton dispersion. A cesium chloride crystal of two nanoparticles with different dipole and quadrupole energies serves as the example structure to show how the plasmon-polariton dispersion depends on the properties of the nanoparticles and supercrystal structure. The tools presented here can be used to predict and analyze any type of optically active excitation in supercrystals. The results show how to differentiate the optical properties of binary nanoparticle supercrystals into properties that inflexibly depend on lattice symmetry and properties that can be finely tuned by choosing the nanoparticle composition and shape.

Exploring the Core Parameters of CNC-Based Chiral Nematic Structures for Enhancing the Dissymmetry Factor of Right-Handed Circularly Polarized Luminescence.

The chiral nematic nanostructure formed from cellulose nanocrystal (CNC) self-assembly has shown great potential as a matrix for generating circularly polarized luminescent (CPL) light with a high dissymmetry factor. Exploring the relationship between the device composition and structure and the light dissymmetry factor is crucial to a common strategy for a strongly dissymmetric CPL light. In this study, we have compared the single-layered and double-layered CNC-based CPL devices with different luminophores, such as rhodamine 6G (R6G), methylene blue (MB), crystal violet (CV), and silicon quantum dots (Si QDs). We demonstrated that forming a double-layered structure of CNCs nanocomposites is a simple but effective pathway for enhancing the CPL dissymmetry factor for CNC-based CPL materials containing different luminophores. The |glum| values of double-layered CNC devices (dye@CNC5||CNC5) versus that of single-layered devices (dye@CNC5) are 3.25 times for Si QDs, 3.7 times for R6G, 3.1 times for MB, and 2.78 times for CV series. The different enhancement degrees of these CNC layers with a similar thickness may be due to the different pitch numbers in the chiral nematic liquid crystal layers whose photonic band gap (PBG) has been modified to match the emission wavelengths of dyes. Furthermore, the assembled CNC nanostructure has great tolerance to the addition of nanoparticles. Gold nanorods coated with the SiO2 layer (Au NR@SiO2) were added for enhancing the dissymmetry factor of MB in CNC composites (named MAS devices). When the strong longitudinal plasmonic band of the Au NR@SiO2 matched the emission wavelength of MB and the PBG of assembled CNC structures simultaneously, the increase in the glum factor and quantum yield of MAS composites was obtained. The good compatibility of the assembled CNC nanostructures makes it a universal platform for developing strong CPL light sources with a high dissymmetry factor.

Facile synthesis of silver-rhenium nanoparticles with plasmonic and mesoporous properties

Cetyltrimethylammonium bromide (CTAB) capped rhenium (Re0@CTA(aq)) NPs were prepared by using chemical reduction method at room temperature in aqueous solution. The resulting Re0@CTA(aq) sol was utilized as sacrificial template and silver ions (Ag+) for the synthesis of silver-rhenium bimetallic NPs (Ag0-Re0@CTA(aq)) under metal displacement galvanic cell reaction in aqueous solution with CTAB. Surface Plasmon resonance (SPR) band intensity and wavelength maxima of Plasmon band of Ag0-Re0@CTA(aq) depends on the concentration of CTAB. The Plasmon band was blue shifted from 434, 439, 519, 535, 465, and 445 nm, respectively, for 0.0, 0.75, 1.0, 1.25, 1.5, and 2.0 mM of CTAB. Oxidation states, crystalline nature, elemental composition, surface morphology, shape, size, and textural properties of as-prepared silver-rhenium were determined with X-ray photoelectron spectrometry (EDX), X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), and nitrogen adsorption-desorption isotherm (BET). Fourier transform infrared spectrometry (FTIR), 1H NMR, 13C NMR, and gas chromatography-mass spectrometry (GC-EIMS) analysis were used to establish the capping properties of CTAB. Application of FTIR, 1H NMR, 13C NMR and GC-EIMS analysis shows that the CTAB consistently remains adsorbed on Ag0-Os0 NPs. Optical properties of plasmonic nanomaterials can be tuned by using a suitable concentration of CTAB surfactant.

Two-Step Synthesis of Large Gold–Silver Alloy Nanoparticles via the Combination of Seeded Growth and Citrate Co-reduction

We report a novel two-step method for the synthesis of uniform quasi-spherical and monodisperse gold–silver alloy nanoparticles with diameters of approximately 80 nm. In step one, gold–silver alloy seeds (G0) with diameters of approximately 30 nm are synthesized by citrate co-reduction of gold acetate and silver nitrate. In step two, the seeds grow into large alloy nanoparticles with diameters of approximately 80 nm by the combination of seeded growth and citrate co-reduction of gold and silver precursors. Our method makes use of gold acetate (rather than chloroauric acid) as a gold precursor to avoid the formation of silver chloride precipitates during synthesis. To our knowledge, we are the first to prepare gold–silver alloy nanoparticles with diameters of above 70 nm using gold acetate as a gold precursor. The alloy seeds and seed-grown nanoparticles show good control of size and composition, which enables tuning of the plasmonic band of these gold–silver alloy nanoparticles. Gold and silver are distributed uniformly within the cores of all Au-Ag alloy nanoparticles, while the surface is enriched in silver. This silver-enriched surface layer is thicker and more prominent for 25% Au alloy nanoparticles than for 50% and 75% Au alloy nanoparticles.

Symmetry-Breaking Effects of Near-Infrared II Thermoplasmonics of Gold–Silica–Cuprous Selenide Hybrid Nanoshells

This study presents a numerical investigation of the plasmonic and photothermal properties of Au-silica-Cu2–xSe hybrid nanoshells (Cu2–xSe HNSs) consisting of a silica-Cu2–xSe core–shell nanoshell embedded with a spherical Au core at varied core offsets. The plasmon modes in the symmetry-broken Cu2–xSe HNSs are explained by plasmon hybridization theory in combination with charge density distribution. Results unveil that the hybridized plasmon modes in a symmetry-broken Cu2–xSe HNS arise from the interaction of the primitive plasmon modes of the same angular momentum on the Au core and the Cu2–xSe nanoshell. An increase in the core offset redshifts and weakens the near-infrared II (NIR-II) plasmon band corresponding to the low-energy bonding dipolar mode but redshifts and enhances the low-energy bonding quadrupolar mode. At the NIR-II plasmon resonance wavelengths, the temperature increase distribution is uniform on the Au core but inhomogeneous on the Cu2–xSe nanoshell. The variation of the temperature increase with the core offset suggests spectral tunability of NIR-II thermoplasmonic properties in the Cu2–xSe HNSs through varying the core offset. Our work provides a paradigm for rational design of NIR-II plasmonic materials with optimal photothermal performances for in vivo biomedical applications through symmetry breaking.

Au@Ag Nanopencil with Au Tip and Au@Ag Rod: Multimodality Plasmonic Nanoprobe based on Asymmetric Etching for the Detection of SCN- and ClO.

In this paper, Au@Ag nanopencil is designed as a multimodality plasmonic nanoprobe based on asymmetric etching for the detection of SCN- and ClO- . Au@Ag nanopencil with Au tip and Au@Ag rod is prepared by asymmetric tailoring of uniformly grown silver-covered gold nanopyramids under the combined effect of partial galvanic replacement and redox reaction. By asymmetric etching in different systems, Au@Ag nanopencil exhibits diversified changes in the plasmonic absorption band: O2 •- facilitated by SCN- etches Au@Ag rod from the end to the tip, causing a blue shift of the localized surface plasmon resonance (LSPR) peak as the aspect ratio decreases; while the ClO- can retain Au@Ag shell and etch Ag within rod from the tip to the end, causing a redshift of the LSPR peak as the coupling resonance weakens. Based on peak shifts in different directions, a multimodality detection of SCN- and ClO- has been established. The results demonstrate the detection limits of SCN- and ClO- are 160 and 6.7nm, and the linear ranges are 1-600µm and 0.05-13µm, respectively. The finely designed Au@Ag nanopencil not only broadens the horizon of designing heterogeneous structures, but also enriches the strategy of constructing multimodality sensing platform.

A Review on Silver Nanoparticles

Nanoparticles are defined as particulate dispersions or solid particles with a size between 10 and 1000 nm. A one billionth of a metre scale is the simplest unit of measurement for nanotechnology. Silver nanoparticles superiority over silver in bulk forms is primarily due to the size, shape, composition, crystallinity, and structure of AgNPs. Silver nanoparticles synthesis can be achieved by physical, chemical and green methods. Evaporation-condensation and laser ablation processes are used in the physical synthesis of silver nanoparticle. Evaporation-condensation has been used to create a number of metal nanoparticles in the past, including fullerene, lead sulphide, cadmium sulphide, gold, and silver. Chemical reduction, photo-induced reduction, micro-emulsion, microwave-assisted synthesis, UV-initiated photo-reduction, electrochemical synthetic technique, and irradiation procedures are some of the chemical processes utilised to create nanoparticles. The temperature, pH, concentration, type of precursor, reducing and stabilising agents, and the molar ratio of surfactant and precursor are some of the reaction parameters that control how NPs form and grow in the chemical method. Utilizing biological organisms like bacteria, mould, algae, and plants allows for one-step synthesis. Proteins and enzymes found in plants and microbes are used in the reduction process to create nanoparticles. Silver nanoparticles function as nanoscale antennas at the plasmon resonant wavelength, boosting the strength of a nearby electromagnetic field. Raman spectroscopy, which uses molecules distinctive vibrational modes to identify them, is one spectroscopic method that benefits from the strengthened electromagnetic field. The plasmonic Au/Ag hollow-shelled NIR SERS probes were put together on silica nanospheres, which showed a redshift in the plasmonic extinction band in the NIR optical window region (700–900 nm). Animal tissues that were 8 mm deep showed a measurable signal in the NIR-SERS nanoprobe signals for single particle detection. Silver nanoparticles size-tunable absorption spectra can be used to multiplex optical attributes for point-of-care diagnostics. Silver nanoparticles have antimicrobial, anti-neoplastic, antioxidant, and antidiabetic activity. Silver nanoparticles also shows some kind of toxicity like Oral toxicity, Immunotoxicity, Neurotoxicity, Environmental toxicity, Reproductive toxicity etc.

Hot hole multiplication from silver plasmon-resonated gold interband transitions for enhanced photoelectrochemical sensing

Compared with the widespread exploitation of hot electrons in plasmonic nanoparticles (NPs), hot holes generated from plasmonic metal interband transitions, are often overlooked in photoelectrochemistry, including photoelectrochemical sensing. Motivated by the subtle spectral overlap between the characteristic plasmonic bands of Ag NPs and interband transitions of Au, herein, we construct unusual core-shell Ag@Au NPs via an anti-galvanic reaction to promote the generation of hot holes. Benefiting from the unique plasmon resonances of Ag cores in specific wavelength regimes, Ag@Au can excite multiplied hot holes while Au cannot under the same conditions. With satisfactory accuracy and good practicability, the photoelectrochemical sensing platform based on Ag@Au NPs possesses a detection limit of 77 nmol/L for glucose, exhibiting significantly higher sensitivity compared to that using Au NPs. This work exemplifies the applications of interband hot-hole accumulation initiated by plasmons and may inspire more strategies to explore the utilization of hot holes in photoelectrochemistry.

Photothermal treatment of glioblastoma cells based on plasmonic nanoparticles.

Photothermal therapy based on plasmonic gold nanoparticles is considered a promising approach for cancer treatment. Here, we investigate the in vitro photothermal effect of 30-nm gold nanoparticles, optically excited with a 532-nm continuous laser, on the U87MG malignant glioblastoma cells, and demonstrate the role of nanoparticle concentration and exposure power density in achieving its optimum performance. Laser-induced collective oscillation of electrons in plasmonic gold nanoparticles is employed to generate localized heat to denature tumor cells. Optical spectroscopy is used to measure the plasmonic band of nanoparticles and select the excitation laser light. The MTT assay for the IC50 viability assessment is performed to evaluate the live and metabolically active cells after treatment with plasmonic nanoparticles. The quantitative data is statistically analyzed using analysis of variance followed by Tukey's post hoc test. The viability test demonstrates that the metabolic activity of treated U87MG was decreased compared with untreated cells, leading to the determination of the IC50 as 92 [Formula: see text]. A 532-nm laser light was selected for the excitation of gold nanoparticles since the maximum plasmonic band is at 524 nm. The viability tests show that although cells have natural photothermal agents, their absorption efficiency is very low; therefore, the laser-induced plasmonic effect is necessary to observe photothermal effects. The optimal condition was achieved when the nanoparticle concentration was 92 [Formula: see text], and the exposure power density was 96 [Formula: see text]. Thus, it is demonstrated that plasmonic nanoparticle concentration and laser exposure power density are among the key parameters in the photothermal treatment of cancer cells, and higher concentrations of Au-NPs and laser power density lead to less cell viability in the selected range due to the excitation of gold nanoparticles' localized surface plasmon resonance.