Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Ag nanoparticle decorated MnO₂ flakes as flexible SERS substrates for rhodamine 6G detection.

ABSTRACT: Smart design of advanced substrates for surface-enhanced Raman scattering (SERS) activity is challenging but vital. Herein, we synthesized a new kind of AgNPs/MnO₂@Al flexible substrate as a SERS substrate for the detection of the analyte rhodamine 6G (R6G). The fabrication of porous MnO₂ nanoflakes on Al foil was conducted via a facile hydrothermal strategy. Owing to the large active surface area of the MnO₂ nanoflakes, the Ag nanoparticles were immobilized and displayed superior SERS performance with a low detection concentration of 1 × 10^-6 M for R6G. In addition, the SERS performance was found to be strongly related to the morphology of the MnO₂@Al substrate material. Our smart design may provide a new method of construction for other advanced SERS substrates for the detection of R6G.

SUBMITTER: Zhang Y

PROVIDER: S-EPMC9089333 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Ag nanoparticle decorated MnO2 flakes as flexible SERS substrates for rhodamine 6G detection.

Zhang Yan Y Liu Rui Jia RJ Ma Xiaofei X Liu Xiao Ying XY Zhang Yu Xin YX Zhang Jie J

RSC advances 20181109 66

Smart design of advanced substrates for surface-enhanced Raman scattering (SERS) activity is challenging but vital. Herein, we synthesized a new kind of AgNPs/MnO2@Al flexible substrate as a SERS substrate for the detection of the analyte rhodamine 6G (R6G). The fabrication of porous MnO2 nanoflakes on Al foil was conducted via a facile hydrothermal strategy. Owing to the large active surface area of the MnO2 nanoflakes, the Ag nanoparticles were immobiliz ...[more]

PMID: 35558625

Similar Datasets

Flower-like Ag-decked non-stoichiometric Bi2O3-x/rGO hybrid nanocomposite SERS substrates for an effective detection of Rhodamine 6G dye molecules.

Project description:In early years, SERS-active substrates were generally noble metals. However, their practical applications were limited due to their poor biocompatibility, low uniformity and high cost. Recently, the utilization of semiconductor SERS-active substrates has greatly expanded the applications of SERS in many fields. However, metal-free SERS-active substrates have a low enhancement factor (EF), which can be overcome by adjusting their oxygen deficiency or through the effective preparation of non-stoichiometric semiconducting oxide materials. This is the key strategy and may work as an efficient and simple way to achieve high sensitivity and obtain an enhancement factor (G-factor) comparable to that of noble metals. Here, we report the preparation of flower-like rGO-Bi2O3/Bi2O2.75 and rGO-Ag-Bi2O3/Bi2O2.75 hybrid thin film nanocomposites using a liquid/liquid interface method (LLI) for the first time. In addition to the synergic effect of different enhancement mechanisms, the 3-D flower-like morphology of the substrate shows more favourable properties to improve the G-factor due to the existence of more hotspots. The rGO-Ag-Bi2O3/Bi2O2.75 hybrid thin-film nanocomposites show an EF of 1.8 × 109 with a detection ability of up to 1 nM towards Rhodamine 6G (R6G), which is highly toxic to humans and the aquatic environment.

| S-EPMC11017965 | biostudies-literature

Highly efficient Ag doped δ-MnO2 decorated graphene: Comparison and application in electrochemical detection of H2O2.

Project description:Cytotoxic H2O2 is an inevitable part of our life, even during this contemporary pandemic COVID-19. Personal protective equipment of the front line fighter against coronavirus could be sterilized easily by H2O2 for reuse. In this study, Ag doped δ-MnO2 nanorods supported graphene nanocomposite (denoted as Ag@δ-MnO2/G) was synthesized as a nonenzymatic electrochemical sensor for the sensitive detection of H2O2. The ternary nanocomposite has overcome the poor electrical conductivity of δ-MnO2 and also the severe aggregation of Ag NPs. Furthermore, δ-MnO2/G provided a rougher surface and large numbers of functional groups for doping more numbers of Ag atoms, which effectively modulate the electronic properties of the nanocomposite. As a result, electroactive surface area and electrical conductivity of Ag@δ-MnO2/G increased remarkably as well as excellent catalytic activity observed towards H2O2 reduction. The modified glassy carbon electrode exhibited fast amperometric response time (<2 s) in H2O2 determination. The limit of detection was calculated as 68 nM in the broad linear range (0.005-90.64 mM) with high sensitivity of 104.43 µA mM-1 cm-2. No significant interference, long-term stability, excellent reproducibility, satisfactory repeatability, practical applicability towards food samples and wastewater proved the efficiency of the proposed sensor.

| S-EPMC8959659 | biostudies-literature

Flexible and Reusable Ag Coated TiO2 Nanotube Arrays for Highly Sensitive SERS Detection of Formaldehyde.

Project description:Quantitative analysis of formaldehyde (HCHO, FA), especially at low levels, in various environmental media is of great importance for assessing related environmental and human health risks. A highly efficient and convenient FA detection method based on surface-enhanced Raman spectroscopy (SERS) technology has been developed. This SERS-based method employs a reusable and soft silver-coated TiO2 nanotube array (TNA) material, such as an SERS substrate, which can be used as both a sensing platform and a degradation platform. The Ag-coated TNA exhibits superior detection sensitivity with high reproducibility and stability compared with other SERS substrates. The detection of FA is achieved using the well-known redox reaction of FA with 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole (AHMT) at room temperature. The limit of detection (LOD) for FA is 1.21 × 10-7 M. In addition, the stable catalytic performance of the array allows the degradation and cleaning of the AHMT-FA products adsorbed on the array surface under ultraviolet irradiation, making this material recyclable. This SERS platform displays a real-time monitoring platform that combines the detection and degradation of FA.

| S-EPMC7179449 | biostudies-literature

Rhodamine 6G conjugated to gold nanoparticles as labels for both SERS and fluorescence studies on live endothelial cells.

Project description:Fluorescence and surface-enhanced Raman scattering (SERS) spectroscopy were employed to investigate the cellular uptake of rhodamine 6G (R6G) alone and of R6G loaded with gold nanoparticles (AuNPs) by endothelial cells. R6G plays the role of a Raman reporter in SERS but also displays strong fluorescence. The presence of bare R6G molecules and R6G-AuNPs in the cytoplasm of the cells is detected via the 2D fluorescence of the dye after a 0.5 h of the incubation with R6G and R6G-AuNPs, and then the concentration of the dye increases within 4 h of exposure. The examination of the cellular uptake of the R6G and R6G-AuNPs species at different temperatures suggests that the internalization of the R6G-AuNPs into endothelial cells occurs mainly via endocytosis. 3D fluorescence imaging of R6G inside cells reveals inhomogeneous distribution of the dye in the cytoplasm. The SERS signal of the Raman reporter inside the cell disappears after 2 h of incubation with R6G-AuNPs and then amino acid residues, purines and pyrimidines become SERS-active via their interactions with the gold. The results highlight the significance of using multiple techniques to cover a spectrum of issues in the application of SERS nanosensors for probing an intracellular environment under comparable and standardized conditions. FigureCellular uptake of bare rhodamine 6G and rhodamine 6G adsorbed onto AuNPs were studied on endothelial cells using fluorescence and surface-enhanced Raman spectroscopy. The internalization of R6G-AuNPs occurs via endocytosis and diffusion resulting in uneven distribution in the cytoplasm.

| S-EPMC4281367 | biostudies-literature

Ag/MnO2 Composite Sheath-Core Structured Yarn Supercapacitors.

Project description:One-dimensional (1D) yarn or fiber-based supercapacitors that have small diameter, volume and high mechanical strength are needed due to the demands on power source for wearable electronics, micro-devices, and implantable medical devices. The composite sheath is fabricated on a commercially available CNT yarn substrate by alternating depositions of MnO2 and Ag layers. Synergistic effect of high loading level of pseudocapacitive MnO2 and reasonably improved rate-capability are achieved. In the composite sheath, the interconnected networks provide electrical contact between MnO2 aggregates and adjacent Ag layer. The conductive Ag inter layers shorten the solid-state charge diffusion length in the MnO2. Moreover, generated electrons during the charge/discharge process can be collected rapidly by the adjacent Ag layer, therefore, the great extents of MnO2 could be loaded onto the surface of CNT core fiber electrode without a significant rate-capability degradation. Due to the high MnO2 loading level, the composite sheath-core yarn supercapacitor showed excellent specific areal capacitance (322.2 mF/cm2) and according energy density (18.3 µWh/cm2).

| S-EPMC6127153 | biostudies-literature

Three-dimensional plasmonic Ag/TiO2 nanocomposite architectures on flexible substrates for visible-light photocatalytic activity.

Project description:In this study, a periodic three-dimensional (3D) Ag/TiO2 nanocomposite architecture of nanowires was fabricated on a flexible substrate to enhance the plasmonic photocatalytic activity of the composite. Layer-by-layer nanofabrication based on nanoimprint lithography, vertical e-beam evaporation, nanotransfer, and nanowelding was applied in a new method to create different 3D Ag/TiO2 nanocomposite architectures. The fabricated samples were characterized by scanning electron microscopy, transmission electron microscopy, focused ion-beam imaging, X-ray photoelectron spectrometry, and UV-visible spectroscopy. The experiment indicated that the 3D nanocomposite architectures could effectively enhance photocatalytic activity in the degradation of methylene blue solution under visible light irradiation. We believe that our method is efficient and stable, which could be applied to various fields, including photocatalysis, solar energy conversion, and biotechnology.

| S-EPMC5566718 | biostudies-literature

Tunable cytotoxicity of rhodamine 6G via anion variations.

Project description:Chemotherapeutic agents with low toxicity to normal tissues are a major goal in cancer research. In this regard, the therapeutic activities of cationic dyes, such as rhodamine 6G, toward cancer cells have been studied for decades with observed toxicities toward normal and cancer cells. Herein, we report rhodamine 6G-based organic salts with varying counteranions that are stable under physiological conditions, display excellent fluorescence photostability, and more importantly have tunable chemotherapeutic properties. Our in vitro studies indicate that the hydrophobic compounds of this series allow production of nanoparticles which are nontoxic to normal cells and toxic to cancer cells. Furthermore, the anions, in combination with cations such as sodium, were observed to be nontoxic to both normal and cancer cells. To the best of our knowledge, this is the first demonstration that both the cation and anion play an extremely important and cooperative role in the antitumor properties of these compounds.

| S-EPMC4197813 | biostudies-literature

Rhodamine 6G hexa-chlorido-stannate(IV) acetonitrile disolvate.

Project description:In the title compound, bis({6-ethylamino-10-[2-(methoxycarbonyl)phenyl]-2,7-dimethylxanthen-3-ylidene}ethanaminium) hexachloridotin(IV) acetonitrile disolvate, (C(27)H(29)N(2)O(3))(2)[SnCl(6)]·2C(2)H(3)N, the octa-hedral SnCl(6) (2-) anion lies on an inversion center. The xanthene ring system is essentially planar, with an average deviation of 0.020 Å, and the substituent benzene ring forms a dihedral angle of 85.89 (2)° with it. The Sn-Cl distances are in the range 2.4237 (3)-2.4454 (3) Å. There are N-H⋯Cl hydrogen bonds between SnCl(6) (2-) ions and rhodamine 6G cations as well as π-π stacking inter-actions between rhodamine 6G cations (inter-planar distance of 3.827 Å).

| S-EPMC2915129 | biostudies-literature

Synthesis and evaluation of the SERS effect of Fe3O4-Ag Janus composite materials for separable, highly sensitive substrates.

Project description:Fe3O4-Ag Janus composites were synthesized using a two-step solvothermal method. The optimal growth process was determined by investigating the relationship between the particle morphologies and reaction time. Magnetic and Raman spectroscopic measurements showed that the as-synthesized Janus composites have both good magnetic response and significant surface-enhanced Raman scattering (SERS) effects, as well as reproducibility. The calculated Raman enhancement factor reached an unprecedented magnitude of 109 compared with the values of other Fe3O4-Ag compounds. Furthermore, the SERS effect was exhibited even at a concentration of probe molecules as low as 10-13 M. This demonstrates that the as-synthesized Fe3O4-Ag Janus composite particles have promise for application as separable, highly sensitive SERS substrates.

| S-EPMC9059953 | biostudies-literature

Controllable Preparation of SERS-Active Ag-FeS Substrates by a Cosputtering Technique.

Project description:In this work, we introduced an ordered metal-semiconductor molecular system and studied the resulting surface-enhanced Raman scattering (SERS) effect. Ag-FeS nanocaps with sputtered films of different thicknesses were obtained by changing the sputtering power of FeS while the sputtering power of Ag and the deposition time remained constant. When metallic Ag and the semiconductor FeS are cosputtered, the Ag film separates into Ag islands partially covered by FeS and strong coupling occurs among the Ag islands isolated by FeS, which contributes to the SERS phenomenon. We also investigated the SERS enhancement mechanism by decorating the nanocap arrays produced with different FeS sputtering powers with methylene blue (MB) probe molecules. As the FeS sputtering power increased, the SERS signal first increased and then decreased. The experimental results show that the SERS enhancement can mainly be attributed to the surface plasmon resonance (SPR) of the Ag nanoparticles. The coupling between FeS and Ag and the SPR displacement of Ag vary with different sputtering powers, resulting in changes in the intensity of the SERS spectra. These results demonstrate the high sensitivity of SERS substrates consisting of Ag-FeS nanocap arrays.

| S-EPMC6384828 | biostudies-literature