Strong Surface Plasmon Research Articles

High-specificity SERS sensing with magnet-powered hierarchically structured micromotors

This work reports a hierarchically structured micromotor (HSM) surface-enhanced Raman scattering (SERS) platform comprising 3D tubular configurations with nanostructured outer walls. The HSMs can be powered by an external magnetic field in solution to enrich molecules with promoted adsorption efficiency. The nanostructured outer wall serves as containers to collect molecules and produce strong localized surface plasmon resonance to intensify Raman of the enriched molecules. Further coupling of HSMs after molecular enrichment can produce additional plasmonic hotspots at the sites where the molecules were enriched, providing a solution to manipulate molecules to enter the plasmonic hotspot region. Moreover, functionalizing specific molecules on the outer wall of HSMs enables high-specificity SERS sensing for benzaldehyde (BA) and Cu2+ ions in liquid. This SERS platform demonstrates great potential for practical applications in biochemical analysis and environmental monitoring, offering a rapid and sensitive tool for detecting low-concentration analytes in liquid.

Investigating SERS performance of controllable fabricated Ag periodic nanostructures with morphologies of nanoclaws and nanocones in detecting SARS-CoV-2 S protein

Surface-enhanced Raman scattering (SERS) spectroscopy plays an important role in enabling high-precision detection and non-invasive diagnostics. Periodic metallic nanostructures with strong electromagnetic fields and tunable localized surface plasmon resonance can achieve high SERS sensitivity, but fabricating such nanostructures remains a challenge. In this work, the anodic aluminum oxide (AAO) nanocavity template-assisted process of fabricating periodic nanostructures with modulating morphologies from Ag nanoclaws (AgNCWs) to Ag nanocones (AgNCEs) is proposed. The morphologies-related SERS performances of nanostructures are analyzed by using rhodamine 6 g (R6G) as a probe molecule and the optimized AgNCEs possess a limit of detection (LOD) of 1 × 10−9 M. A sandwich strategy is applied to detect SARS-CoV-2 S protein in phosphate-buffered saline (PBS) and pharyngeal swab solution (PSS). The ACE2-modified AgNCEs (ACE2/AgNCEs) structure is applied to bind to the SARS-CoV-2 S protein. The 4-MBA and SARS-CoV-2 S antibody functionalized Au nanoparticles (AuNPs) are used as nanotags. By forming the ACE2/AgNCEs-SARS-CoV-2 S protein-nanotags sandwich structure, characteristic peak intensities of 1580 cm−1 are used as the report signal, and the LOD for SARS-CoV-2 S protein in PBS and PSS solution are 10 fg/mL.

Avi-tag mediated Phage@gold nanoprobe illuminates bacteria

The phage demonstrates specific recognition towards its host bacteria, while the gold nanoparticle (GNP) exhibits a strong surface plasmon resonance (SPR) effect and emits visible fluorescence with dark-field microscope (DFM). Therefore, phage modified with multiple GNPs (phage@GNPs) targeting bacteria enables the visualization of targets under DFM. However, a universal strategy for constructing a stable phage nanoprobe suitable for clinical detection remains a challenge. Herein, we developed a GNP-functionalized phage (phage@GNPs) by displaying an AVI-tag at the N-terminal region of the major capsid protein in S55 (a Salmonella phage). The S55 displaying AVI-tag exhibits equivalent infectivity towards various serotypes of Salmonella as the native S55 and can be further biotinylated through a reaction between lysine residues on the AVI-tag and COOH groups on D-biotin mediated. Consequently, biotinylated S55 was mixed with streptavidin functionalized GNPs to generate the S55@GNPs due to the strong interaction between biotin and streptavidin. Analysis results showed that the obtained S55@GNPs maintained native affinity to host bacteria and better monodispersity and stability than the other four modification and assembly methods for constructing phage@GNPs. Furthermore, the results of simulated and clinical Salmonella samples demonstrated that AVI-tag mediated S55@GNPs probes possess a qPCR-like sensitivity with a detection limit of 1 CFU/μL. Notably, the remarkable AVI-tag mediated phage@GNPs DFM strategy covers an extensive detection range spanning from 1 to 50,000 CFU/μL. Additionally, we employed the AVI-tag mediated assemble of phage@GNPs for phages of Vibrio and Klebsiella. The results showed similar data as S55 for illuminating host cells, suggesting that AVI-tag mediated phage@GNPs assembly is a universal strategy applicable to phage of any other bacteria for illuminating their respective host bacterial under DFM.

Synthesis and photocatalytic activity of Ag/AgCl for removal of BTX vapors under visible light: modeling by ANN

Abstract Among volatile organic compounds, benzene, toluene, and xylene (BTX) are the most harmful organic compounds and the removal of these harmful compounds is mandatory. In the current study, Ag/AgCl composite was successfully synthesized via deposition–precipitation along with the photoreduction method. The scanning electron microscopy, x-ray powder diffraction, photoluminescence spectroscopy, Fourier transform infrared spectra, and ultraviolet-visible diffuse reflectance spectroscopy were employed to characterize the synthesized products. The photocatalytic property of the products was investigated by evaluating on photodegradation of BTX vapors under the radiation of visible light. The results showed that Ag/AgCl exhibits enhanced visible-light photocatalytic activity compared with AgCl. The strong surface plasmon resonance of metal Ag nanoparticles anchored on the AgCl surface can be responsible for the enhanced visible-light photocatalytic activity of the Ag/AgCl. The influence of the basic operational parameters such as type of BTX, the concentration of BTX, photocatalyst shape, relative humidity, and radiation time on the removal efficiency of BTX was studied. The data obtained from removal tests were modeled by a three-layered feed-forward artificial neural network. The optimized ANN architecture was strong at predicting the removal efficiency of the BTX contaminants with R2 > 0.99 and a very low mean square error. The sensitivity analysis using Garson’s method displayed that all explored process parameters influence the photocatalytic removal of the BTX contaminants. The obtained ANN model is used to predict the photodegradation of BTX at different conditions.

Gold Nanoparticles: Multifunctional Properties, Synthesis, and Future Prospects.

Gold nanoparticles (NPs) are among the most commonly employed metal NPs in biological applications, with distinctive physicochemical features. Their extraordinary optical properties, stemming from strong localized surface plasmon resonance (LSPR), contribute to the development of novel approaches in the areas of bioimaging, biosensing, and cancer research, especially for photothermal and photodynamic therapy. The ease of functionalization with various ligands provides a novel approach to the precise delivery of these molecules to targeted areas. Gold NPs' ability to transfer heat and electricity positions them as valuable materials for advancing thermal management and electronic systems. Moreover, their inherent characteristics, such as inertness, give rise to the synthesis of novel antibacterial and antioxidant agents as they provide a biocompatible and low-toxicity approach. Chemical and physical synthesis methods are utilized to produce gold NPs. The pursuit of more ecologically sustainable and economically viable large-scale technologies, such as environmentally benign biological processes referred to as green/biological synthesis, has garnered increasing interest among global researchers. Green synthesis methods are more favorable than other synthesis techniques as they minimize the necessity for hazardous chemicals in the reduction process due to their simplicity, cost-effectiveness, energy efficiency, and biocompatibility. This article discusses the importance of gold NPs, their optical, conductivity, antibacterial, antioxidant, and anticancer properties, synthesis methods, contemporary uses, and biosafety, emphasizing the need to understand toxicology principles and green commercialization strategies.

In Situ Deprotection-Free Synthesis of Silver/Graphdiyne with a High Raman Sensing Effect for Detection of Polychlorophenols and Microplastics.

Since the first synthesis of graphdiyne (GDY), it has been widely receiving a lot of attention and has great application prospects in many fields, such as energy storage, catalysis, and sensing. However, the complex deprotection treatment and long reaction time limit its mass production and applications. Here, we present a strategy for the silver-catalyzed deprotection-free rapid synthesis of GDY. Crystalline GDY was synthesized in 8 h at room temperature and atmospheric pressure, and after the reaction, Ag nanoparticles with an ultrathin diameter of 2-3 nm were formed in situ inside and on the surface of GDY. This Ag/GDY composite exhibits a high specific surface area of 672.3 m2 g-1 and strong surface plasmon resonance behavior, showing a strong surface-enhanced Raman scattering effect. The enhancement factor and the lowest detection limit for rhodamine 6G are 3.54 × 108 and 1 × 10-14 M, respectively. The Ag/GDY achieves the simultaneous enrichment and detection of polychlorophenols and ultrafine nanoplastics.

Highly sensitive, reproducible, and stable core–shell MoN SERS substrate synthesized via sacrificial template method

Molybdenum nitride is a promising candidate for surface-enhanced Raman scattering (SERS) substrates due to its high conductivity, surface plasmon resonance, and chemical stability. Core-shell structures possess unique physical and chemical properties, such as high-volume ratio, low density, short diffusion length, and high load-bearing capacity, making them favorable for SERS applications. In this research, core–shell MoO3 is first synthesized as a precursor oxide using a sacrificial template method, and core–shell MoN microspheres are successfully prepared via subsequent nitriding. As a representative transition metal nitride, the obtained core–shell MoN nanospheres show strong localized surface plasmon resonance and SERS effects. Using these MoN microspheres as Raman substrates allows a range of highly targeted compounds to be accurately detected, and the detection limits for this non-precious-metal substrate morphology are exceptionally high, reaching 10−10 M. In addition, MoN nanospheres exhibit excellent resistance to acid–base corrosion, oxidation, and radiation, thus rendering them suitable for use as substrates in harsh environments.

Silver Nanoparticles in Therapeutics and Beyond: A Review of Mechanism Insights and Applications.

Silver nanoparticles (NPs) have become highly promising agents in the field of biomedical science, offering wide therapeutic potential due to their unique physicochemical properties. The unique characteristics of silver NPs, such as their higher surface-area-to-volume ratio, make them ideal for a variety of biological applications. They are easily processed thanks to their large surface area, strong surface plasmon resonance (SPR), stable nature, and multifunctionality. With an emphasis on the mechanisms of action, efficacy, and prospective advantages of silver NPs, this review attempts to give a thorough overview of the numerous biological applications of these particles. The utilization of silver NPs in diagnostics, such as bioimaging and biosensing, as well as their functions in therapeutic interventions such as antimicrobial therapies, cancer therapy, diabetes treatment, bone repair, and wound healing, are investigated. The underlying processes by which silver NPs exercise their effects, such as oxidative stress induction, apoptosis, and microbial cell membrane rupture, are explored. Furthermore, toxicological concerns and regulatory issues are discussed, as well as the present difficulties and restrictions related to the application of silver NPs in medicine.

Plasmonic semi shells derived from simultaneous in situ gold growth and anisotropic acid etching of ZIF-8 for photothermal ablation of metastatic breast tumor

Open nanoshells such as nanobowls or nanocups collectively described as ‘semi shells’ have unique plasmonic properties due to their lack of symmetry. So far, their fabrication was based on multistep and laborious methods such as solid state sputter coating or selective deposition/etching using sacrificial templates. In this work, we report a rapid one step colloidal synthetic protocol for PEGylated semi-shell (SS) fabrication by simultaneous facet specific anisotropic chemical etching of rhombic dodecahedral ZIF-8 and heterogenous nucleation & growth of gold. The SS possesses a strong localized surface plasmon resonance in the near-infrared region, which is retained after surface passivation with polyethylene glycol and subsequent cryopreservation for extended shelf-life. Freshly reconstituted PEGylated SS was found to be safe & non-toxic in healthy C57BL/6 mice post intravenous administration. The PEGylated SS displayed significant photothermal efficiency of ~37% with 808 nm laser irradiation. Preclinical assessment of intra-tumoral photothermal efficacy indicated complete remission of primary breast tumor mass with insignificant metastasis to vital organs in 4T1 FL2 tumor bearing CD1 nude mice. Further, PEGylated SS mediated photothermal therapy also yielded morbidity free survivael of 75% for up to 90 days, indicating their potential to significantly improve outcomes in advanced breast tumors.

Aggregated gold nanoparticles rich in electromagnetic field “hotspots” for surface enhanced Raman scattering

A simple method for one-step synthesis of aggregated gold nanoparticles (a-AuNPs) using single-layer carbon dots (s-CDs) as the capping agents has been proposed. The obtained a-AuNPs are mainly composed of several spherical AuNPs of 20–25 nm sized, which aggregate to form nanogaps of ∼1 nm. Furthermore, the obtained a-AuNPs produce a strong localized surface plasmon resonance (LSPR) absorption band centered at around 640 nm, which is quite close to the wavelength of the commonly used 633 nm laser in surface enhanced Raman scattering (SERS). Thus, under the irradiation of 633 nm laser, a lot of electromagnetic field “hot spots” are formed at around the nanogaps, and strong SERS activity is achieved. The obtained a-AuNPs are dropped on tin-foil wafers to fabricate SERS substrates, which show the advantages of high sensitivity, fast response, good repeatability and satisfactory stability. On the basis, a sensitive SERS sensor is developed to detect malachite green in aquaculture water, with a low detection limit of 1 × 10−9 mol/L.

Titanium boride nanosheets with photo-enhanced sonodynamic efficiency for glioblastoma treatment

Sonodynamic therapy (SDT) has garnered significant attention in cancer treatment, however, the low-yield reactive oxygen species (ROS) generation from sonosensitizers remains a major challenge. In this study, titanium boride nanosheets (TiB2 NSs) with photo-enhanced sonodynamic efficiency was fabricated for SDT of glioblastoma (GBM). Compared with commonly-used TiO2 nanoparticles, the obtained TiB2 NSs exhibited much higher ROS generation efficiency under ultrasound (US) irradiation due to their narrower band gap (2.50 eV). Importantly, TiB2 NSs displayed strong localized surface plasmon resonance (LSPR) effect in the second near-infrared (NIR II) window, which facilitated charge transfer rate and improved the separation efficiency of US-triggered electron–hole pairs, leading to photo-enhanced ROS generation efficiency. Furthermore, TiB2 NSs were encapsulated with macrophage cell membranes (CM) and then modified with RGD peptide to construct biomimetic nanoagents (TiB2@CM-RGD) for efficient blood-brain barrier (BBB) penetrating and GBM targeting. After intravenous injection into the tumor-bearing mouse, TiB2@CM-RGD can efficiently cross BBB and accumulate in the tumor sites. The tumor growth was significantly inhibited under simultaneous NIR II laser and US irradiation without causing appreciable long-term toxicity. Our work highlighted a new type of multifunctional titanium-based sonosensitizer with photo-enhanced sonodynamic efficiency for GBM treatment. Statement of significanceTitanium boride nanosheets (TiB2 NSs) with photo-enhanced sonodynamic efficiency was fabricated for SDT of glioblastoma (GBM). The obtained TiB2 NSs displayed strong localized surface plasmon resonance (LSPR) effect in the second near-infrared (NIR II) window, which facilitated charge transfer rate and improved the separation efficiency of US-triggered electron-hole pairs, leading to photo-enhanced ROS generation efficiency. Furthermore, TiB2 NSs were encapsulated with macrophage cell membranes (CM) and then modified with RGD peptide to construct biomimetic nanoagents (TiB2@CM-RGD) for efficient blood-brain barrier (BBB) penetrating and GBM targeting. After intravenous injection into the tumor-bearing mouse, TiB2@CM-RGD can efficiently cross BBB and accumulate in the tumor sites. The tumor growth was significantly inhibited under simultaneous NIR II laser and US irradiation without causing appreciable long-term toxicity.

Simulation study of multi-layer titanium nitride nanodisk broadband solar absorber and thermal emitter

Solar energy has always been a kind of energy with large reserves and wide application. It is well utilized through solar absorbers. In our study, the finite difference time domain method (FDTD) is used to simulate the absorber composed of refractory metal materials, and its absorption performance and thermal emission performance are obtained. The ultra-wide band of 200 nm–3000 nm reaches 95.93% absorption efficiency, of which the bandwidth absorption efficiency of 2533 nm (200 nm–2733 nm) is greater than 90%. The absorption efficiency in the whole spectrum range (200 nm–2733 nm) is 97.17% on average. The multilayer nanodisk structure of the absorber allows it to undergo strong surface plasmon resonance and near-field coupling when irradiated by incident light. The thermal emission performance of the absorber enables it to also be applied to the thermal emitter. The thermal emission efficiency of 95.37% can be achieved at a high temperature of up to 1500 K. Moreover, the changes of polarization and incident angle do not cause significant changes in absorption. Under the gradual change of polarization angle (0°–90°), the absorption spectrum maintains a high degree of consistency. As the incident angle increases from 0° to 60°, there is still 85% absorption efficiency. The high absorption efficiency and excellent thermal radiation intensity of ultra-wideband enable it to be deeply used in energy absorption and conversion applications.

Plasmon-enhanced photoelectrochemical-SERS simultaneous dual-read-out determination of enrofloxacin based on bifunctional Bi2S3 quantum dots/triangular Ag nanoparticles/Ti3C2 MXene heterojunction

The exploration of high-efficiency detection technologies of antibiotic residues plays vital roles for the evaluation of food quality and environmental safety risks owing to the adverse effects of antibiotics, which could accelerate the emergence of antibiotic-resistant genes. Herein, an integrated complementary dual-mode sensor was developed based on Bi2S3 quantum dots/triangular silver nanoparticles/Ti3C2 MXene (Bi2S3 QDs/T-Ag NPs/Ti3C2) heterojunction by in-situ coupling photoelectrochemical (PEC) analysis with surface-enhanced Raman spectroscopy (SERS) method. The bifunctional heterojunction could enhance light absorption, boost the generation of the electron-hole pairs, and facilitate the light-matter interactions, resulting in increased photoelectric conversion efficiency and enhanced Raman scattering for sensing applications. Moreover, the unique triangular shape and strong surface plasmon resonance effect of T-Ag NPs were conducted to further enhance the output signals of the dual-mode sensing platform. Such as-fabricated PEC/SERS detection system offered good complementarity and achieved mutually check via the combination of the inherent characteristics of two individual modes, which provided more accurate measurement results and more convincing information. Further, aptamer was adopted to recognize enrofloxacin molecules, which could achieve selective and sensitive detection of target. The detection limit of PEC and SERS was calculated as 0.61 fM (S/N = 3) and 0.21 fM (S/N = 3), respectively. Besides, the dual-mode aptasensor exhibited excellent stability and reproducibility, showing a promising prospect to detect enrofloxacin in real samples.

Selenium-Doped Seeded Growth of Truncated Octahedral Gold Nanocrystals with Surface Concavities for Surface-Enhanced Raman Spectroscopy.

Concave nanocrystals stand out as a testament to the importance of the nanoscale morphology in dictating the functional properties of materials. In this report, we introduce a facile synthesis method for producing gold (Au) nanocrystals with a truncated octahedral morphology that features surface concavities (Au CNTOs). The incorporation of selenium (Se) doping into the truncated octahedral Au seeds was essential for their enlargement and the formation of concave structures. By simply adjusting the quantity of seeds, we could control the size of the nanocrystals while maintaining their distinctive morphology and surface concavity. The formation mechanism suggests that Se doping likely passivates the side faces, thereby slowing growth and promoting atomic deposition at the edges and corners. The resulting Se-doped Au CNTOs exhibited strong localized surface plasmon resonance (LSPR) absorptions in the visible spectrum and the SERS performance of their assemblies was demonstrated through crystal violet detection, reaching enhancement factors around 105. This study presents an innovative approach to synthesizing concave Au nanocrystals through the incorporation of selenium during a seeded growth process, offering insights into the strategic design of plasmonic nanostructures.

Simultaneous noninvasive ultrasensitive detection of prostate specific antigen and lncRNA PCA3 using multiplexed dual optical microfibers with strong plasmonic nanointerfaces

Low accuracy of diagnosing prostate cancer (PCa) was easily caused by only assaying single prostate specific antigen (PSA) biomarker. Although conventional reported methods for simultaneous detection of two specific PCa biomarkers could improve the diagnostic efficiency and accuracy, low detection sensitivity restrained their use in extreme early-stage PCa clinical assay applications. In order to overcome above drawbacks, this paper herein proposed a multiplexed dual optical microfibers separately functionalized with gold nanorods (GNRs) and Au nanobipyramids (Au NBPs) nanointerfaces with strong localized surface plasmon resonance (LSPR) effects. The sensors could simultaneously detect PSA protein biomarker and long noncoding RNA prostate cancer antigen 3 (lncRNA PCA3) with ultrahigh sensitivity and remarkable specificity. Consequently, the proposed dual optical microfibers multiplexed biosensors could detect the PSA protein and lncRNA PCA3 with ultra-low limit-of-detections (LODs) of 3.97 × 10−15 mol/L and 1.56 × 10−14 mol/L in pure phosphorus buffer solution (PBS), respectively, in which the obtained LODs were three orders of magnitude lower than existed state-of-the-art PCa assay technologies. Additionally, the sensors could discriminate target components from complicated physiological environment, that showing noticeable biosensing specificity of the sensors. With good performances of the sensors, they could successfully assay PSA and lncRNA PCA3 in undiluted human serum and urine simultaneously, respectively. Consequently, our proposed multiplexed sensors could real-time high-sensitivity simultaneously detect complicated human samples, that providing a novel valuable approach for the high-accurate diagnosis of early-stage PCa individuals.

Atomic‐Thin 2D Copper Sulfide Nanocrystals with over 94% Photothermal Conversion Efficiency as Superior NIR‐II Photoacoustic Agents

AbstractExploring photothermal nanomaterials is essential for new energy and biomedical applications; however, preparing materials with intense absorption, highly efficient light‐to‐heat conversion, and enhanced photostability still faces the enduring challenge. Herein, the study synthesizes atomic‐thin (≈1.6 nm) 2D copper sulfide (AT‐CuS) plasmonic nanocrystals and find its extraordinary photothermal conversion efficiency (PCE) reaching up to 94.3% at the second near‐infrared (NIR‐II) window. Photophysical mechanism studies reveal that the strong localized surface plasmon resonance (LSPR) and out‐of‐plane size effect of AT‐CuS induce strong optical absorption and non‐equilibrium carrier scattering, resulting in a significant carrier‐phonon coupling (7.18 × 1017 J K−1 s−1 m−3), ultimately enhancing the heat generation. Such a photothermal nanomaterial demonstrates at leastmes stronger NIR‐II photoacoustic (PA) signal intensity than that of most commonly used miniature gold nanorods, together with greater biocompatibility and photo‐/thermal‐stability, enabling noninvasive PA imaging of brain microvascular in living animals. This work provides an insight into the rational exploration of superb NIR‐II photothermal and photoacoustic agents for future practical utilizations.

Metallic Degenerately Doped Free-Electron-Confined Plasmonic Nanocrystal and Infrared Extinction Response

In this paper, synthetically scaled-up degenerately n-type doped indium tin oxide (Sn:In2O3) nanocrystals are described as highly transparent conductive materials possessing both optoelectronic and crystalline properties. With tin dopants serving as n-type semiconductor materials, they can generate free-electron carriers. These free electrons, vibrating in resonance with infrared radiation, induce strong localized surface plasmon resonance (LSPR), resulting in efficient infrared absorption. To commercialize products featuring Sn:In2O3 with localized surface plasmon resonance, a scaled-up synthetic process is essential. To reduce the cost of raw materials during synthesis, we aim to proceed with synthesis in a large reactor using industrial raw materials. Sn:In2O3 can be formulated into ink dispersed in solvents. Infrared-absorbing ink formulations can capitalize on their infrared absorption properties to render opaque in the infrared spectrum while remaining transparent in the visible light spectrum. The ink can serve as a security ink material visible only through infrared cameras and as a paint absorbing infrared light. We verified the transparency and infrared absorption properties of the ink produced in this study, demonstrating consistent characteristics in scaled-up synthesis. Due to potential applications requiring infrared absorption properties, it holds significant promise as a robust platform material in various fields.

Mesoporous platinum@copper selenide-based NIR-II photothermal agents with photothermal conversion efficiency over 80% for photoacoustic imaging and targeted cancer therapy

Elevating photothermal conversion efficiency (PCE) is the key to enhance curative efficacy during photothermal therapy. Nevertheless, current functionalized or synthetic methods for preparing photothermal agents with high PCE are too complicated, greatly hindering the development of photothermal therapy. In this study, we developed a tumor-targeting flower-like nanocomposite termed mesoporous platinum nanoparticles@Cu2-xSe-AS1411 (MPNPs@Cu2-xSe-AS1411, denoted as MPCSA) with remarkable PCE for high-resolution photoacoustic (PA) imaging guided photothermal/chemodynamic therapy for tumor ablation. We discovered that MPNPs served as carriers for delivering PA contrast agents. Cu2-xSe nanosheets emerged as promising near-infrared-II (NIR-II) PA imaging and photothermal/chemodynamic therapy agents owing to their strong localized surface plasmon resonance property in the NIR-II region. The amine-modified AS1411 aptamer, which is connected to the surface of the flower-like MPNPs@Cu2-xSe can target the nucleolar protein on the surface of 4T1 cells, achieving the accumulation of MPCSA at the tumor site in mice. Notably, these MPCSA nano-flowers exhibited an excellent PCE up to 82.33 % under 1064 nm laser irradiation, resulting in highly efficient cancer cell ablation and greatly hindering in vivo tumor growth. This study has paved the way for imaging-guided accurate cancer diagnosis and targeted cancer therapy.

Photothermal properties of Cu@polycarbonate composites with strong localized surface plasmon resonances

Photothermal properties of Cu@polycarbonate composites with strong localized surface plasmon resonances

Plasmonic Bound States in the Continuum Metasurface-Semiconductor-Metal Architecture Enables Efficient Hot-Electron-Based Photodetector.

Plasmonic hot-electron-based photodetectors (HEB-PDs) have received widespread attention for their ability to realize effective carrier collection under sub-bandgap illumination. However, due to the low hot electron emission probability, most of the existing HEB-PDs exhibit poor responsivity, which significantly restricts their practical applications. Here, by employing the binary-pore anodic alumina oxide template technique, we proposed a compact plasmonic bound state in continuum metasurface-semiconductor-metal-based (BIC M-S-M) HEB-PD. The symmetry-protected BIC can manipulate a strong gap surface plasmon in the stacked M-S-M structure, which effectively enhances light-matter interactions and improves the photoresponse of the integrated device. Notably, the optimal M-S-M HEB-PD with near-unit absorption (∼90%) around 800 nm delivers a responsivity of 5.18 A/W and an IPCE of 824.23% under 780 nm normal incidence (1 V external bias). Moreover, the ultrathin feature of BIC M-S-M (∼150 nm) on the flexible substrate demonstrates excellent stability under a wide range of illumination angles from -40° to 40° and at the curvature surface from 0.05 to 0.13 mm-1. The proposed plasmonic BIC strategy is very promising for many other hot-electron-related fields, such as photocatalysis, biosensing, imaging, and so on.