Gold Nanosheets Research Articles

Synergistic antibacterial effects of selenium-doped gold nanosheets with notable near infrared-II photothermal conversion against multidrug-resistant bacteria

Non-metallic nanoparticles are increasingly acknowledged for their broad-spectrum antibacterial properties, which often face limitations due to structural instability and potential biotoxicity. To address these challenges, integrating non-metallic nanoparticles with plasmonic metal nanostructures offers a promising solution. This fusion not only enhances structural stability but also reduces the required dosage. The synergistic coupling of the inherent antibacterial properties of non-metallic nanoparticles with the plasmonic absorption and photothermal conversion capabilities of metal nanostructures significantly amplifies antibacterial efficacy. In this study, we validate this concept by presenting the successful synthesis of selenium-doped gold nanosheets (AuSe NSs) that demonstrate robust absorption in the second near-infrared (NIR-II) window and exhibit efficient photothermal conversion, followed by testing their antibacterial activity. Notably, Au NSs were synthesized with high shape purity, followed by the introduction of SeO2 and ascorbic acid to facilitate Se doping. The resulting products displayed a uniform distribution of both Au and Se elements, while maintaining the NIR-II absorbance characteristic of Au nanosheets unaffected by the Se doping as evidenced by both experimental and FDTD simulation results. Subsequent assessments of the AuSe NSs demonstrated their potent synergistic antibacterial effects against multidrug-resistant bacteria at minimal inhibitory concentrations (MICs), which suggests that lower dosages can be employed and benefit minimizing potential side effects and optimizing treatment efficiency. Our findings indicate a synergistic boost between the photothermal attributes originating from Au's NIR absorption and Se's inherent antibacterial properties—an aspect minimally explored in prior research and offering a novel solution to tackling antibiotic-resistant bacterial strains.

Tailor-Made Gold Nanomaterials for Applications in Soft Bioelectronics and Optoelectronics.

In modern nanoscience and nanotechnology, gold nanomaterials are indispensable building blocks that have demonstrated a plethora of applications in catalysis, biology, bioelectronics, and optoelectronics. Gold nanomaterials possess many appealing material properties, such as facile control over their size/shape and surface functionality, intrinsic chemical inertness yet with high biocompatibility, adjustable localized surface plasmon resonances, tunable conductivity, wide electrochemical window, etc. Such material attributes have been recently utilized for designing and fabricating soft bioelectronics and optoelectronics. This motivates to give a comprehensive overview of this burgeoning field. The discussion of representative tailor-made gold nanomaterials, including gold nanocrystals, ultrathin gold nanowires, vertically aligned gold nanowires, hard template-assisted gold nanowires/gold nanotubes, bimetallic/trimetallic gold nanowires, gold nanomeshes, and gold nanosheets, is begun. This is followed by the description of various fabrication methodologies for state-of-the-art applications such as strain sensors, pressure sensors, electrochemical sensors, electrophysiological devices, energy-storage devices, energy-harvesting devices, optoelectronics, and others. Finally, the remaining challenges and opportunities are discussed.

Highly Conductive and Stretchable Hydrogel Nanocomposite Using Whiskered Gold Nanosheets for Soft Bioelectronics.

The low electrical conductivity of conductive hydrogels limits their applications as soft conductors in bioelectronics. This low conductivity originates from the high water content of hydrogels, which impedes facile carrier transport between conductive fillers. This study presents a highly conductive and stretchable hydrogel nanocomposite comprising whiskered gold nanosheets. A dry network of whiskered gold nanosheets is fabricated and then incorporated into the wet hydrogel matrices. The whiskered gold nanosheets preserve their tight interconnection in hydrogels despite the high water content, providing a high-quality percolation network even under stretched states. Regardless of the type of hydrogel matrix, the gold-hydrogel nanocomposites exhibit a conductivity of ≈520Scm-1 and a stretchability of ≈300% without requiring a dehydration process. The conductivity reaches a maximum of ≈3304Scm-1 when the density of the dry gold network is controlled. A gold-adhesive hydrogel nanocomposite, which can achieve conformal adhesion to moving organ surfaces, is fabricated for bioelectronics demonstrations. The adhesive hydrogel electrode outperforms elastomer-based electrodes in in vivo epicardial electrogram recording, epicardial pacing, and sciatic nerve stimulation.

Gold Nanoparticles-Modified 2D Self-Assembled Amphiphilic Peptide Nanosheets with High Biocompatibility and Photothermal Therapy Efficiency.

Amphiphilic peptides have garnered significant attention due to their highly designable and self-assembling behaviors. Self-assembled peptides hold excellent potential in various fields such as biosensing, environmental monitoring, and drug delivery, owing to their remarkable biological, physical, and chemical properties. While nanomaterials formed by peptide self-assembly have found widespread use in biomedical applications, the development of 2D peptide nanosheets based on the self-assembly of amphiphilic peptides remains challenging in terms of rational design and morphology modulation. In this study, rationally designed amphiphilic peptide molecules are self-assembled into peptide nanosheets (PNS) under specific conditions to encapsulate gold nanoparticles (AuNPs), resulting in the formation of AuNPs/PNS hybrid materials with high photothermal conversion efficiency. The findings demonstrate that 2D PNS enhances the overall photothermal therapy effect of the nanohybrid materials due to their larger hosting area for AuNPs and higher biocompatibility. The well-designed amphiphilic peptides in this study offer insights into the structural design and functional modulation of self-assembled molecules. In addition, the constructed biomimetic-functional 2D inorganic/organic nanohybrid materials hold potential applications in biomedical engineering.

Rapid fluorescent nucleic acid sensing with ultra-thin gold nanosheets

Fluorescently labeled DNA oligonucleotides and gold nanospheres have been frequently utilized in biosensors, providing efficient nucleic acid detection. Nevertheless, the restricted loading capacity of gold nanospheres undermines overall sensitivity. In this study, we employed four-atom-thick ultrathin gold nanosheets (AuNSs), utilizing a “pre-mix model” for rapid target nucleic acid detection. In this approach, fluorescently labeled DNA probes were pre-incubated with the target nucleic acid, followed by the addition of AuNSs for probe adsorption and fluorescence quenching. With the developed method, we efficiently and rapidly detected the SARS-CoV-2 N gene sequence within 30 min, involving a brief 15-min target pre-incubation and a subsequent 15-min adsorption of free probes and fluorescence quenching by AuNSs. This method exhibited heightened sensitivity compared to gold nanospheres, boasting a limit of detection (LOD) of 0.808 nM. Furthermore, exceptional recovery was achieved in simulated biological samples. The study introduces an effective strategy for nucleic acid sensing characterized by rapidity, heightened sensitivity, ease of operation, and robustness. These findings encourage further development of rapid biomarker sensing methods employing 2D nanomaterials.

An ultrasensitive electrochemical/colorimetric dual-mode self-powered biosensing platform for lung cancer marker detection by multiple-signal amplification strategy

BackgroundIn recent years, miRNAs have emerged as potentially valuable tumor markers, and their sensitive and accurate detection is crucial for early screening and diagnosis of tumors. However, the analysis of miRNAs faces significant challenges due to their short sequence, susceptibility to degradation, high similarity, low expression level in cells, and stringent requirements for in vitro research environments. Therefore, the development of sensitive and efficient new methods for the detection of tumor markers is crucial for the early intervention of related tumors. ResultsAn ultrasensitive electrochemical/colorimetric dual-mode self-powered biosensor platform is established to detect microRNA-21 (miR-21) via a multi-signal amplification strategy. Gold nanoparticles (AuNPs) and VS4 nanosheets self-assembled 3D nanorods (VS4-Ns-Nrs) are prepared for constructing a superior performance enzyme biofuel cell (EBFC). The double-signal amplification strategy of Y-shaped DNA nanostructure and catalytic hairpin assembly (CHA) is adopted to further improve enhance the strength and specificity of the output signal. In addition, a capacitor is matched with EBFC to generate an instantaneous current that is amplified several times, and the output detection signal is improved once more. At the same time, electrochemical and colorimetric methods are used for dual-mode strategy to achieve the accuracy of detection. The linear range of detection is from 0.001 pg/mL to 1000 pg/mL, with a relatively low limit of detection (LOD) of 0.16 fg/mL (S/N = 3). SignificanceThe established method enables accurate and sensitive detection of markers in patients with lung cancer, providing technical support and data reference for precise identification. It is anticipated to offer a sensitive and practical new technology and approach for early diagnosis, clinical treatment, and drug screening of cancer and other related major diseases.

Gold nanosheet modified electrode with reduced impedance for electrophysiological recordings

In neurophysiological recording, reducing electrode impedance is crucial for enhancing the signal-to-noise ratio and achieving the desired spatial resolution. This study presents an approach to improve the performance of Au/Cr/glass electrodes by incorporating synthesized gold nanosheets without the need for additional adhesive material. We characterized the performance of the modified electrodes using electrochemical impedance spectroscopy and equivalent circuit analysis. Our findings showed an 81% reduction in mean impedance for the modified electrode, which was 0.85 kΩ at 1 kHz, compared to the unmodified electrode at 4.5 kΩ, an improvement attributed to the higher effective surface area of the modified electrode. Additionally, Scanning electron microscopy observations of PC12 cells cultured on the modified electrodes indicated favorable cell elongation and interaction with the rough surface. Stability studies indicated acceptable performance of the modified electrodes in solution environments. These results suggest that surface modification of electrodes with gold nanosheets could be a promising strategy for enhancing neural interface applications.

A stretchable, fully self-healable, temperature-tolerant, and water-proof supercapacitor using TUEG3 capped gold nanosheets on oxime-carbamate bonded polyurethane film and organohydrogel

In this study, we demonstrate a stretchable, fully self-healable, temperature-tolerant, and water-proof supercapacitor with high electrochemical performance via a deliberate selection of materials and device architecture. Distinct from previous works, our whole supercapacitor is stretchable and self-healable, owing to the application of specially devised stretchable and self-healing oxime-carbamate based polyurethane (OC-PU) substrate film, self-healing polymer (poly(ether-thioureas) triethylene glycol) capped Au nanosheet current collector (TUEG3-Au NS) and newly synthesized organohydrogel electrolyte. The fabricated supercapacitor exhibits a high electrochemical performances (specific capacitance of 165.5F g−1, energy density of 14.58 Wh kg−1, power density of 2181.75 W kg−1, and capacitance retention of 89 % after 10,000 cycles) with a capacitance retention of 81 % over stretching by 40 % even after repetitive healing from damages, the self-healing of all components (full self-healing) over repetitive damages with a capacitance recovery by over 83 %, a wide operational temperature range from −20 to 60 °C with retaining over 91 % of capacitance at RT. Furthermore, a μ-LED is stably operated with the supercapacitor immersed in water regardless of the mechanical deformation and self-healing from damage due to self-bonded encapsulation layer of hydrophobic OC-PU film. With a vertically integrated patch device consisting of the fabricated supercapacitor and a strain sensor, bio-signals are detected using the stored energy of the supercapacitor even after self-healing from damages over the temperature range from −20 to 60 °C. This work suggests the high application potential of our high performance multi-functional supercapacitor as an integrated energy storage device for wearable electronics featuring longevity and stability under harsh environments.

DNA Framework-Templated Fabrication of Ultrathin Electroactive Gold Nanosheets.

Generally, two-dimensional gold nanomaterials have unique properties and functions that offer exciting application prospects. However, the crystal phases of these materials tend to be limited to the thermodynamically stable crystal structure. Herein, we report a DNA framework-templated approach for the ambient aqueous synthesis of freestanding and microscale amorphous gold nanosheets with ultrathin sub-nanometer thickness. We observe that extended single-stranded DNA on DNA nanosheets can induce site-specific metallization and enable precise modification of the metalized nanostructures at predefined positions. More importantly, the as-prepared gold nanosheets can serve as an electrocatalyst for glucose oxidase-catalyzed aerobic oxidation, exhibiting enhanced electrocatalytic activity (~3-fold) relative to discrete gold nanoclusters owing to a larger electrochemical active area and wider band gap. The proposed DNA framework-templated metallization strategy is expected to be applicable in a broad range of fields, from catalysis to new energy materials.

DNA Framework‐Templated Fabrication of Ultrathin Electroactive Gold Nanosheets

AbstractGenerally, two‐dimensional gold nanomaterials have unique properties and functions that offer exciting application prospects. However, the crystal phases of these materials tend to be limited to the thermodynamically stable crystal structure. Herein, we report a DNA framework‐templated approach for the ambient aqueous synthesis of freestanding and microscale amorphous gold nanosheets with ultrathin sub‐nanometer thickness. We observe that extended single‐stranded DNA on DNA nanosheets can induce site‐specific metallization and enable precise modification of the metalized nanostructures at predefined positions. More importantly, the as‐prepared gold nanosheets can serve as an electrocatalyst for glucose oxidase‐catalyzed aerobic oxidation, exhibiting enhanced electrocatalytic activity (~3‐fold) relative to discrete gold nanoclusters owing to a larger electrochemical active area and wider band gap. The proposed DNA framework‐templated metallization strategy is expected to be applicable in a broad range of fields, from catalysis to new energy materials.

Enhancing near-infrared II photothermal conversion through anchoring numerous nanospheres to the edge of a gold nanosheet

Two-dimensional gold (Au) in-plane hybrid nanostructures are rationally designed with numerous quasi-spherical particles adorning the edge of a single plate, showcasing promising use in NIR-II photothermal conversion.

Lattice dynamics study of gold nanotube

We have developed an analytical analysis based on lattice dynamics theory to study phonon dispersion relation for gold nanotube. This paper gives an overview of the methodology for calculating of phonon dispersion of gold nanotube using an example of small gold nanosheet. The dynamical matrix for the gold nanosheet was calculated using the force constants derived from Gupta Potential (GP). A better understanding of properties of gold nanotube is useful for its quick characterisation for possible applications in bio sensing, imaging etc. This work may be helpful in formulating algebra for calculating the phonon dispersion of gold nanotube and can be further used for calculating properties such as specific heat, thermal conductivity etc. at low computational cost in comparison with first principle calculations.

Development of Ultrasensitive New Sensor Based on Functionalized Triangular Gold Nanosheets Layers for SARS-CoV-2 Detection

Development of Ultrasensitive New Sensor Based on Functionalized Triangular Gold Nanosheets Layers for SARS-CoV-2 Detection

Au/CrSe stacked layers designed as optical absorbers, tunneling barriers and negative capacitance sources

Herein thin films of CrSe (500 nm) are deposited onto glass and semitransparent gold nanosheets (100 nm) under a vacuum pressure of 10−5 mbar. Au nanosheets substrates induced the formation of CrSe instead of CrSe2 which grows onto glass substrates. The Au/CrSe stacked layers exhibited enhanced light absorption reaching 25% in the ultraviolet, visible and infrared ranges of light. In addition Au nanosheets successfully redshifted the direct allowed transitions energy band gap from 2.60 eV to 2.40 eV. On the other hand electrical investigations have shown that CrSe2 thin films exhibit a work function of 5.064 eV. The Au/CrSe interfaces displayed tunneling type Schottky barriers of height of 0.56 eV and barrier width of 8 nm. When an ac signal was imposed between the terminals of the Au/CrSe Schottky barriers a negative capacitance (NC) effects was observed in the spectral range of 0.02–1.80 GHz. The NC reached value of − 100 pF at 0.32 GHz. Fitting of the ac conductivity assuming tunneling type of transport indicated a high degree of localization near the Fermi level reaching a density of 2.4×1020 cm−3 eV−1. The enhanced light absorption and moderate value of work function in addition to the tunneling type of Schottky formation performing as NC source make the Au/CrSe interfaces promising for use in the design of electro-optic system.

Charge-state effects on charge transfer of helium ions in gold nanosheet

We investigate the charge-state effects on charge transfer of helium ions in gold nanosheet using the time-dependent density functional theory non-adiabatically coupled to the molecular dynamics. In order to characterize and extract the charge-state information of incident particles inside the nanosheet, we develop two novel computational methods. It is found that the charge transfer behavior of He ion in gold nanosheet is sensitive to its charge state at the time of incident. Analysis of these results allows us to gain new insights in the interaction between He ions and gold nanosheet. This work validates the ability of current methodology in dealing with ion collisions in materials.

Optical Control of the Localized Surface Plasmon Resonance in a Heterotype and Hollow Gold Nanosheet.

The remote excitation and remote-controlling of the localized surface plasmon resonance (LSPR) in a heterotype and hollow gold nanosheet (HGNS) is studied using FDTD simulations. The heterotype HGNS contains an equilateral and hollow triangle in the center of a special hexagon, which forms a so-called hexagon-triangle (H-T) heterotype HGNS. If we focus the incident-exciting laser on one of the vertexes of the center triangle, the LSPR could be achieved among other remote vertexes of the outer hexagon. The LSPR wavelength and peak intensity depend sensitively on factors such as the polarization of the incident light, the size and symmetry of the H-T heterotype structure, etc. Several groups of the optimized parameters were screened out from numerous FDTD calculations, which help to further obtain some significant polar plots of the polarization-dependent LSPR peak intensity with two-petal, four-petal or six-petal patterns. Remarkably, based on these polar plots, the on-off switching of the LSPR coupled among four HGNS hotspots could be remote-controlled simply via only one polarized light, which shows promise for its potential application in remote-controllable surface-enhanced Raman scattering (SERS), optical interconnects and multi-channel waveguide switches.

A colorimetric assay for detection of glucose by enzymatic etching of triangular gold nanosheets

Blood glucose detection is an essential of diabetes management, so it is urgent to develop a convenient and practical blood glucose monitoring method. Herein, a colorimetric assay for detection of glucose based on enzymatic etching of triangular gold nanosheets was reported. In the presence of glucose oxidase (GOD) catalyzed the oxidation of glucose to produce hydrogen peroxide (H2O2), which induced the etching of triangular gold nanosheets (AuTNPs) from the corner, leading to the blue shift in absorption peak. Both enzymatic reaction and H2O2 etching can lead to the localized surface plasmon resonance (LSPR) displacement. In this paper, the theoretical simulation, DLS measurement, TEM test and UV–vis absorption spectra experiment are combined to verify that the detection mechanism is etching, and it is verified that the etching starts from the corners of the triangle and gradually reaches the surface. At the same time, the sensor has a wide detection range. In addition, the ratio and concentration of EDC/NHS, pH value of phosphate buffered solution (PBS), GOD concentration and reaction temperature were studied, and the best detection conditions of glucose were determined. Under the optimal detection conditions, this glucose colorimetric sensor exhibits excellent sensing performance in the glucose range of 0.2–12 mM and the limit of detection is limit 0.1 mM (S/N = 3). In addition, glucose was tested in artificial fluids. The results demonstrated that the colorimetric analysis based on triangular gold nanosheets-glucose oxidase system performs in artificial fluids as well as in phosphate buffer solution, making it very suitable for the clinical diagnosis of diabetes.

Spectrophotometric Analysis and Optimization of 2D Gold Nanosheet Formation.

Free-standing, 2D gold nanosheets (AuNS) offer broad potential applications from computing to biosensing and healthcare. Such applications, however, require improved control of material growth. We recently reported the synthesis of AuNS only ∼0.47 nm (two atoms) thick, which exhibited very high catalytic activity. The synthesis is a one-pot, seedless procedure in which chloroauric acid is reduced by sodium citrate in the presence of methyl orange (MO). In this study, we use spectrophotometric analysis and TEM imaging to probe AuNS formation and optimize the procedure. Previously, we suggested that MO acted as the confining agent, directing two-dimensional growth of the gold. Here, we provide the first reported analysis of the HAuCl4 and MO reaction. We show that MO is rapidly oxidized to give 4-diazobenzenesulfonic acid, indicating that a complex interplay between HAuCl4, MO, and other reaction products leads to AuNS formation. Time-resolved studies indicate that synthesis time can be significantly reduced from over 12 to 2-3 h. Decreasing the reaction temperature from 20 to 4 °C improved AuNS yield by 16-fold, and the catalytic activity of the optimized material matches that obtained previously. Our elucidation of AuNS formation mechanisms has opened avenues to further improve and tune the synthesis, enhancing the potential applications of ultrathin AuNS.

Precise Photothermal Treatment of Methicillin-Resistant S. aureus Infection via Phage Lysin-Cell Binding Domain-Modified Gold Nanosheets.

The increasing spread of antibiotic resistance in bacterial pathogens poses a huge threat to global human health. Precise targeting of bacterial pathogens while avoiding collateral damage to healthy tissues has become the overriding goal for bacterial infection treatment. Inspired by the host specificity of bacteriophages, a biomimetic intelligent platform was designed for highly precise photothermal treatment herein. As proof-of-concept, the lysin cell-binding domain (CBD) from a newly discovered virulent methicillin-resistant S. aureus (MRSA) phage Z was applied to the functionalization of gold nanosheets. Our results demonstrated that the bionanocomposite gold particles (Au@PEG-CBDz) could be effectively delivered directly to MRSA and kill them effectively under near infrared irradiation in vitro, while displaying good in vivo biocompatibility. This work is the first to report the combination of phage lysin navigatory function with photothermal effect-induced bactericidal activity from Au nanosheets, providing a novel therapeutic mode for the precision treatment of antibiotic-resistant bacterial infections.

Quasi-Two-Dimensional Gold Nanosheets with Ultrahigh Strength

Quasi-Two-Dimensional Gold Nanosheets with Ultrahigh Strength