Organotrialkoxysilane-mediated synthesis of functional noble metal nanoparticles and their bimetallic for electrochemical recognition of L-tryptophan

MRS Advances ◽  
2020 ◽  
Vol 5 (46-47) ◽  
pp. 2429-2444
Author(s):  
P.C. Pandey ◽  
Shubhangi Shukla ◽  
Govind Pandey ◽  
Roger J. Narayan
Keyword(s):  
Modified Electrode ◽  
Noble Metal ◽  
Limit Of Detection ◽  
High Sensitivity ◽  
Differential Pulse ◽  
Noble Metal Nanoparticles ◽  
Core Shell ◽  
Oxidation Potentials ◽  
Wide Range ◽  
Sequential Reduction

AbstractEffective and pH-sensitive electrochemical monitoring of L-tryptophan using noble metal nanocatalysts was evaluated in this study. This work examined the electrocatalytic influence of nanoparticles on the oxidation of amino acids with the variation of pH in working media. Bimetallic nanohybrids of palladium, silver, and gold (e.g., Pd/Ag and Pd/Au nanoparticles) were processed using organofunctionalized alkoxysilanes (3-aminopropyltrimethoxysilane (3-APTMS) and 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (EETMOS)) via a sequential reduction pathway. Transmission electron microscopy (TEM) demonstrated the role of the alkoxysilanes in determining the size of the nanoparticles and the distribution of metals in the core-shell configuration. The cluster-like morphology of PdNPs was remodeled to form bimetallic nanomaterials (Pd-AuNPs and Pd-AgNPs) with a core-shell structure. Enhancement in the electrooxidation behavior was shown to depend on the nanomaterial and the pH of the medium. The Pd-AgNPs modified electrode exhibited high sensitivity and selectivity, with characteristic amplification in cathodic peak current at lower oxidation potentials (0.659 V, 0.782 V, and 0.890 V at pH values 4, 7, and 9, respectively) due to its greater stability. Differential pulse voltammetric (DPV) scans were recorded over a wide range of concentrations from 0.1 μM to 1000μM; the Pd-AgNPs modified electrode showed the lowest limit of detection of 0.1μM at pH 4, 0.5 μM at pH 7, and 0.5 μM at pH 9.

scholarly journals Copper-nickel oxide nanofilm modified electrode for non-enzymatic determination of glucose

2020 ◽  
Vol 10 (3) ◽  
pp. 245-255
Author(s):  
Mahsa Hasanzadeh ◽  
Zahra Hasanzadeh ◽  
Sakineh Alizadeh ◽  
Mehran Sayadi ◽  
Mojtaba Nasiri Nezhad ◽  
...  
Keyword(s):  
Modified Electrode ◽  
Limit Of Detection ◽  
High Sensitivity ◽  
Stability Loss ◽  
The Novel ◽  
Step Potential ◽  
Enzymatic Determination ◽  
Wide Range ◽  
Naoh Solution

CuxO-NiO nanocomposite film for the non-enzymatic determination of glucose was prepared by the novel modifying method. At first, anodized Cu electrode was kept in a mixture solution of CuSO4, NiSO4 and H2SO4 for 15 minutes. Then, a cathodization process with a step potential of -6 V in a mixture solution of CuSO4 and NiSO4 was initiated, generating formation of porous Cu-Ni film on the bare Cu electrode by electrodeposition assisted by the release of hydrogen bubbles acting as soft templates. Optimized conditions were determined by the experimental design software for electrodeposition process. Afterward, Cu-Ni modified electrode was scanned by cyclic voltammetry (CV) method in NaOH solution to convert Cu and Ni nanoparticles to the nano-scaled CuxO-NiO film. The electrocatalytic behavior of the novel CuxO-NiO film toward glucose oxidation was studied by CV and chronoamperometry (CHA) techniques. The calibration curve of glucose was found linear in a wide range of 0.04–5.76 mM, with a low limit of detection (LOD) of 7.3 µM (S/N = 3) and high sensitivity (1.38 mA mM-1 cm-2). The sensor showed high selectivity against some usual interfering species and high stability (loss of only 6.3 % of its performance over one month). The prepared CuxO-NiO nanofilm based sensor was successfully applied for monitoring glucose in human blood serum and urine samples.

Electrochemical Sensors Based on Noble Metal Nanoparticles in Voltammetry

2021 ◽  
Vol 887 ◽  
pp. 54-59
Author(s):  
D.O. Perevezentseva ◽  
Eduard V. Gorchakov
Keyword(s):  
Metal Nanoparticles ◽  
Noble Metal ◽  
Electrochemical Sensors ◽  
Narrow Range ◽  
Spherical Shape ◽  
High Sensitivity ◽  
Noble Metal Nanoparticles ◽  
Wide Range ◽  
Sulfur Containing

Portable electrochemical sensors based on noble metal nanoparticles (МеNPs) for the quantitative determination of hydrogen peroxide (H2O2) and sulfur-containing amino acids (cysteine, methionine, glutathione) are discussed. These sensors have high sensitivity (pM), with low sample requirements (<50 μl). This article discusses methods for producing sensors based on silver and gold nanoparticles and their application in voltammetry. It is shown that the sensitivity of H2O2 determination on a sensor based on silver nanoparticles (AgNPs) depends on their size. Their size is determined by the reducing agent. Sensors based on AgNPs of spherical shape with the smallest size from 0.5 to 17.5 nm have the highest sensitivity for determining H2O2, but a narrow range of determined concentrations. Sensors on medium-sized AgNPs have optimal metrological characteristics. Their size is from 10 to 55 nm, less sensitive, but with a wide range of determined concentrations from 0.1 to 1 nm H2O2. The linearity of the range of glutathione concentrations is 1.0-10.0 pM. The linearity of the range of determined concentrations of methionine is 1–26 рМ.

scholarly journals Ag nanoparticles outperform Au nanoparticles for the use as label in electrochemical point-of-care sensors

2021 ◽  
Author(s):  
Franziska Beck ◽  
Carina Horn ◽  
Antje J. Baeumner
Keyword(s):  
Limit Of Detection ◽  
Point Of Care ◽  
Automatic Measurement ◽  
High Sensitivity ◽  
Differential Pulse ◽  
Small Sample ◽  
Blood Protein ◽  
User Friendliness ◽  
Response Curves ◽  
Assay Protocol

AbstractElectrochemical immunosensors enable rapid analyte quantification in small sample volumes, and have been demonstrated to provide high sensitivity and selectivity, simple miniaturization, and easy sensor production strategies. As a point-of-care (POC) format, user-friendliness is equally important and most often not combinable with high sensitivity. As such, we demonstrate here that a sequence of metal oxidation and reduction, followed by stripping via differential pulse voltammetry (DPV), provides lowest limits of detection within a 2-min automatic measurement. In exchanging gold nanoparticles (AuNPs), which dominate in the development of POC sensors, with silver nanoparticles (AgNPs), not only better sensitivity was obtained, but more importantly, the assay protocol could be simplified to match POC requirements. Specifically, we studied both nanoparticles as reporter labels in a sandwich immunoassay with the blood protein biomarker NT-proBNP. For both kinds of nanoparticles, the dose-response curves easily covered the ng∙mL−1 range. The mean standard deviation of all measurements of 17% (n ≥ 4) and a limit of detection of 26 ng∙mL−1 were achieved using AuNPs, but their detection requires addition of HCl, which is impossible in a POC format. In contrast, since AgNPs are electrochemically less stable, they enabled a simplified assay protocol and provided even lower LODs of 4.0 ng∙mL−1 in buffer and 4.7 ng∙mL−1 in human serum while maintaining the same or even better assay reliability, storage stability, and easy antibody immobilization protocols. Thus, in direct comparison, AgNPs clearly outperform AuNPs in desirable POC electrochemical assays and should gain much more attention in the future development of such biosensors.

Core-shell Cu@C@ZIF-8 composite: a high-performance electrode material for electrochemical sensing of nitrite with high selectivity and sensitivity

2021 ◽  
Author(s):  
Feng Gao ◽  
Xiaolong Tu ◽  
Yongfang Yu ◽  
Yansha Gao ◽  
Jin Zou ◽  
...  
Keyword(s):  
High Performance ◽  
High Selectivity ◽  
Limit Of Detection ◽  
Metal Organic Framework ◽  
High Sensitivity ◽  
Electrochemical Sensing ◽  
Core Shell ◽  
Zeolitic Imidazolate Framework ◽  
Sensing Platform ◽  
The Difference

Abstract Herein, an efficient electrochemical sensing platform is proposed for selective and sensitive detection of nitrite on the basis of Cu@C@Zeolitic imidazolate framework-8 (Cu@C@ZIF-8) heterostructure. Core-shell Cu@C@ZIF-8 composite was synthesized by pyrolysis of Cu-metal-organic framework@ZIF-8 (Cu-MOF@ZIF-8) in Ar atmosphere on account of the difference of thermal stability between Cu-MOF and ZIF-8. For the sensing system of Cu@C@ZIF-8, ZIF-8 with proper pore size allows nitrite diffuse through the shell, while big molecules cannot, which ensures high selectivity of the sensor. On the other hand, Cu@C as electrocatalyst promotes the oxidation of nitrite, thereby resulting high sensitivity of the sensor. Accordingly, the Cu@C@ZIF-8 based sensor presents excellent performance for nitrite detection, which achieves a wide linear response range of 0.1 µM to 300.0 µM, and a low limit of detection (LOD) of 0.033 µM. In addition, the Cu@C@ZIF-8 sensor possesses excellent stability and reproducibility, and was employed to quantify nitrite in sausage samples with recoveries of 95.45-104.80%.

scholarly journals Noble Metal Composite Porous Silk Fibroin Aerogel Fibers

Materials ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 894 ◽  
Author(s):  
Alexander Mitropoulos ◽  
F. Burpo ◽  
Chi Nguyen ◽  
Enoch Nagelli ◽  
Madeline Ryu ◽  
...  
Keyword(s):  
Noble Metal ◽  
Silk Fibroin ◽  
Noble Metals ◽  
Metal Salt ◽  
Supercritical Drying ◽  
Noble Metal Nanoparticles ◽  
Metal Composite ◽  
Composite Aerogel ◽  
Wide Range ◽  
Composite Aerogels

Nobel metal composite aerogel fibers made from flexible and porous biopolymers offer a wide range of applications, such as in catalysis and sensing, by functionalizing the nanostructure. However, producing these composite aerogels in a defined shape is challenging for many protein-based biopolymers, especially ones that are not fibrous proteins. Here, we present the synthesis of silk fibroin composite aerogel fibers up to 2 cm in length and a diameter of ~300 μm decorated with noble metal nanoparticles. Lyophilized silk fibroin dissolved in hexafluoro-2-propanol (HFIP) was cast in silicon tubes and physically crosslinked with ethanol to produce porous silk gels. Composite silk aerogel fibers with noble metals were created by equilibrating the gels in noble metal salt solutions reduced with sodium borohydride, followed by supercritical drying. These porous aerogel fibers provide a platform for incorporating noble metals into silk fibroin materials, while also providing a new method to produce porous silk fibers. Noble metal silk aerogel fibers can be used for biological sensing and energy storage applications.

scholarly journals Noble Metal Nanoparticles-Based Colorimetric Biosensor for Visual Quantification: A Mini Review

Chemosensors ◽  
2019 ◽  
Vol 7 (4) ◽  
pp. 53 ◽  
Author(s):  
Lu Yu ◽  
Na Li
Keyword(s):  
Metal Nanoparticles ◽  
Noble Metal ◽  
Electrostatic Interactions ◽  
Organic Molecules ◽  
Chemical Reduction ◽  
Noble Metal Nanoparticles ◽  
Gold And Silver Nanoparticles ◽  
Local Surface Plasmon Resonance ◽  
Reliable Technique ◽  
Wide Range

Nobel metal can be used to form a category of nanoparticles, termed noble metal nanoparticles (NMNPs), which are inert (resistant to oxidation/corrosion) and have unique physical and optical properties. NMNPs, particularly gold and silver nanoparticles (AuNPs and AgNPs), are highly accurate and sensitive visual biosensors for the analytical detection of a wide range of inorganic and organic compounds. The interaction between noble metal nanoparticles (NMNPs) and inorganic/organic molecules produces colorimetric shifts that enable the accurate and sensitive detection of toxins, heavy metal ions, nucleic acids, lipids, proteins, antibodies, and other molecules. Hydrogen bonding, electrostatic interactions, and steric effects of inorganic/organic molecules with NMNPs surface can react or displacing capping agents, inducing crosslinking and non-crosslinking, broadening, or shifting local surface plasmon resonance absorption. NMNPs-based biosensors have been widely applied to a series of simple, rapid, and low-cost diagnostic products using colorimetric readout or simple visual assessment. In this mini review, we introduce the concepts and properties of NMNPs with chemical reduction synthesis, tunable optical property, and surface modification technique that benefit the development of NMNPs-based colorimetric biosensors, especially for the visual quantification. The “aggregation strategy” based detection principle of NMNPs colorimetric biosensors with the mechanism of crosslinking and non-crosslinking have been discussed, particularly, the critical coagulation concentration-based salt titration methodology have been exhibited by derived equations to explain non-crosslinking strategy be applied to NMNPs based visual quantification. Among the broad categories of NMNPs based biosensor detection analyses, we typically focused on four types of molecules (melamine, single/double strand DNA, mercury ions, and proteins) with discussion from the standpoint of the interaction between NMNPs surface with molecules, and DNA engineered NMNPs-based biosensor applications. Taken together, NMNPs-based colorimetric biosensors have the potential to serve as a simple yet reliable technique to enable visual quantification.

scholarly journals Magnetic and Mesoporous Silica-Niobia Material as Modifier of Carbon Paste Electrode for p-Nitrophenol Electrochemical Determination

2021 ◽  
Author(s):  
Oleg Tkachenko ◽  
Danielle da Rosa ◽  
Anike Virgili ◽  
Marcos Vasconcellos ◽  
Tania Costa ◽  
...  
Keyword(s):  
Mesoporous Silica ◽  
Carbon Paste Electrode ◽  
Electrochemical Sensors ◽  
Limit Of Detection ◽  
Sol Gel ◽  
Synthesis Method ◽  
Differential Pulse ◽  
Carbon Paste ◽  
Wide Range ◽  
Paste Electrode

In the present work, the sol-gel synthesis method was employed as strategy to obtain a magnetic and mesoporous silica-niobia material. The planned synthesis was based on the heterocondensation of niobium and silicon alkoxide precursors, in the presence of spherical magnetite particles. The resulting material presented interesting characteristics such as magnetism, large mesopores, in the range from 20 to 50 nm, and 68 m2 g−1 of surface area. These features allowed its use as modifier of carbon paste electrode for p-nitrophenol determination, since niobia has never been used in electrochemical sensors for the determination of nitrophenol compounds. By using differential pulse voltammetry technique, the electrode can be applied in a wide range of p-nitrophenol concentration, from 10 to 490 μmol L−1, with a limit of detection of 1.2 µmol L−1 and sensitivity up to 0.60 µA L µmol−1. The proposed electrode presented good sensitivity and selectivity and it was applied in real water samples.

scholarly journals SIMULTANEOUS ELECTROCHEMICAL DETECTION OF ASCORBIC ACID, DOPAMINE, AND URIC ACID AT MAGNETIC NANOPARTICLES/REDUCED GRAPHENE OXIDE MODIFIED ELECTRODE

2021 ◽  
Vol 83 (3) ◽  
pp. 85-92
Author(s):  
Azleen Rashidah Mohd Rosli ◽  
Farhanini Yusoff ◽  
Saw Hong Loh ◽  
Hanis Mohd Yusoff ◽  
Muhammad Mahadi Abdul Jamil ◽  
...  
Keyword(s):  
Ascorbic Acid ◽  
Uric Acid ◽  
Graphene Oxide ◽  
Magnetic Nanoparticles ◽  
Reduced Graphene Oxide ◽  
Modified Electrode ◽  
Limit Of Detection ◽  
Simultaneous Detection ◽  
Differential Pulse ◽  
Reduced Graphene

A magnetic nanoparticles/reduced graphene oxide modified glassy carbon electrode (MNP/rGO/GCE) was fabricated via one-step facile synthesis route for the simultaneous determination of ascorbic acid (AA), dopamine (DA), along with uric acid (UA). A series of diseases and disorders has been associated with irregular levels of these respective analytes, thus early detection is highly crucial. Physical and electrochemical characterization of the modified electrode was conducted by using Scanning Electron Microscopy (SEM), Fourier Transform Infrared (FTIR) analysis, X-Ray Diffraction (XRD) analysis and Brauneur-Emmet-Teller (BET), Cyclic Voltammetry (CV) and Electron Impedance Spectroscopy (EIS). The results obtained confirmed the formation of MNP/rGO composite. Differential pulse voltammetry (DPV) of MNP/rGO/GCE displays three well-defined peaks which associated to AA, DA and UA, respectively. The response towards DA is linear in the concentration range of 15 nM to 100 µM with a detection limit of 0.19 nM while a response to AA and UA is also linear in the concentration range of 10 µM to 100 µM with a limit of detection 0.22 µM and 45 nM respectively. The proposed modified electrode offers a good response towards simultaneous detection of three different electroactive species with excellent electron transfer rate, great capacitance and ideal diffusive control behavior.

scholarly journals Preparation and Application of Keggin Silicomolybdic acid Modified Electrode

2020 ◽  
Author(s):  
Miao Liu ◽  
Mingxuan Jia ◽  
Dong Hui Li
Keyword(s):  
Glassy Carbon Electrode ◽  
Modified Electrode ◽  
Glassy Carbon ◽  
Photoelectron Spectroscopy ◽  
Limit Of Detection ◽  
Differential Pulse ◽  
Carbon Electrode ◽  
X Ray ◽  
Linear Relationships

Abstract An innovative method for the determination of isoniazid tablets is studied through electrochemical method for the modification of glassy carbon electrode (GCE). Polyoxomolybdate, with stable structures, has not been widely used for the determination of substance. In this study, the mentioned polyoxomolybdate was characterized by Fourier transform infrared spectroscopy (FT-IR), UV-vis, X-ray diffraction (XRD), Atomic force microscope (AFM) and X-ray photoelectron spectroscopy (XPS), and used to modify the glassy carbon electrode. The electrochemical performance of the polyoxomolybdate@GCE was investigated with cyclic voltammetry (CV) and differential pulse voltammetry (DPV), compared with the unmodified electrode, the proposed polyoxomolybdate modified electrode exhibited strong electro-catalytic activities towards isoniazid (INH). Under the optimized conditions, there was linear relationships between the DPV peak currents and the concentrations in the range of 1 × 10 -7 g/L to 3 × 10 -7 g/L for INH (R 2 = 0.9979), with the limit of detection (LOD) of 0.024 μg/L (based on S/N = 3). The modified electrode has proper reproducibility (RSD < 5%), stability, response time (< 3 min) and lifetime (up to 6 days).

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