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The electrocatalytic activity and electronic conductivity of 2D transition metal chalcogenides are usually enhanced by as follows the ideal strategy such as doping or substitution heterogeneous atoms. Here, a rare Earth metal ion of gadolinium (Gd3+) was doped with MoSe2 and synthesized through the hydrothermal method. The morphology and nanostructure of Gd3+ with MoSe2 spheres were analyzed under X-ray diffraction, Fourier-transform infrared spectroscopy, X-ray photoelectron, High-resolution transmission electron microscopy analysis, Field emission scanning electron microscopy, and energy-dispersive spectroscopy. Furthermore, the Gd3+ doped MoSe2 sphere modified glassy carbon electrode (Gd@MoSe2/GCE) was used for the sensing of tryptophan. The Gd@MoSe2 modified GCE shows remarkable sensing performance of tryptophan resulting in a linear range (20 nM–220 μM) with a low detection limit (6.7 nM). Under the optimal condition, the developed electrochemical sensor was successfully used to determine tryptophan (TRP) in blood serum and milk samples. The electrochemical biosensing results suggest that the doping of the Gd3+ doped MoSe2 sensor is a promising electrocatalyst in biological and food samples.

In recent years, transition metal dichalcogenides have become increasingly popular in electrochemical sensors due to their excellent redox properties. Herein, a highly efficient electrocatalyst Gd3+ doped molybdenum selenide with carbon nanofibers (Gd-MoSe2/CNF) is synthesized for electrocatalytic sensing of H2S. The synthesis involves a facile and quick hydrothermal treatment. The morphological, elemental, electrochemically active surface area, and impedance properties were investigated to understand its sensing capability. Gd-MoSe2/CNF showed excellent electrocatalytic ability to oxidize H2S. The overpotential for oxidation was minimized to +0.10 V, Ag/AgCl, and the response current increased two-fold compared to control electrodes. High sensitivity, acceptable selectivity, robustness and appreciable reproducibility were observed. The linear range was 12.5 nM–1.2 mM and the detection limit was 1 nM. The method was successful in tracking H2S secreted by HeLa cells. Our reports suggest that Gd-MoSe2/CNF is a useful material in monitoring endogenous H2S.

There is an urgent need to develop in situ sensors that monitor the continued release of H2S from biological systems to understand H2S-related pathology and pharmacology. For this purpose, we have developed a molybdenum disulfide supported double-layered zinc cobaltite modified carbon cloth electrode (MoS2–ZnCo2O4–ZnCo2O4) based electrocatalytic sensor. The results of our study suggest that the MoS2–ZnCo2O4–ZnCo2O4 electrode has excellent electrocatalytic ability to oxidize H2S at physiological pH, in a minimized overpotential (+0.20 vs. Ag/AgCl) with an amplified current signal. MoS2 grown on double-layered ZnCo2O4 showed relatively better surface properties and electrochemical properties than MoS2 grown on single-layered ZnCo2O4. The sensor delivered excellent analytical parameters, such as low detection limit (5 nM), wide linear range (10 nM–1000 μM), appreciable stability (94.3%) and high selectivity (2.5-fold). The practicality of the method was tested in several major biological fluids. The electrode monitors the dynamics of bacterial H2S in real-time for up to 5 h with good cell viability. Our research shows that MoS2–ZnCo2O4–ZnCo2O4/carbon cloth is a robust and sensitive electrode to understand how bacteria seek to adjust their defense strategies under exogenously induced stress conditions.

A robust real-time quantification method is essential to understand the physiological roles of endogenous H2O2 in biological systems. For this purpose, we described a binary transition-metal oxide ...

A three-dimensional hierarchical network of bismuth nanoparticles decorated graphene-carbon nanotubes nanocomposite (Bi NPs@Gr-CNTs) was synthesized and employed for electrocatalytic detection of mercury (Hg (II)). The electrocatalyst was characterized via scanning electron microscopy, transmission electron microscopy, Energy-dispersive X-ray spectroscopy, X-ray diffraction, FT-IR, electrochemical impedance spectroscopy, and cyclic voltammetry. The electrocatalytic activity of Bi NPs@Gr-CNTs modified screen-printed carbon electrode (SPCE) toward Hg (II) was studied using cyclic voltammetry, and differential pulse voltammetry. The Bi NPs@Gr-CNTs/SPCE exhibited excellent electrocatalytic ability to Hg (II) in comparison to control electrodes. Under optimized conditions, Bi NPs@Gr-CNTs/SPCE exhibits excellent Hg (II) sensing attributes in the range of 1.0 nM–217.4 µM with 0.2 nM of detection limit. The electrode was specific for Hg (II) in presence of other metal ions ascribe excellent selectivity. Practicality of the method was demonstrated in tap water, fish oil tablet, human serum, and urine samples (spiked method), which presented acceptable recoveries.

A copper-1,4-naphthalenedicarboxylic acid-based organic framework (Cu-NDCA MOF) with different morphologies was synthesized by solvothermal synthetic route via a simple protonation–deprotonation approach. The synthesized Cu-NDCA MOFs were analyzed by diverse microscopic and spectral techniques. The FE-SEM and TEM image results exhibited the flake-like (FL), partial anisotropic (PAT), and anisotropic (AT)-Cu-NDCA MOFs formation obtained at different pH (3.0, 7.0, and 9.0) of the reaction medium. The AT-Cu-NDCA MOF/GC electrode not only increases the electroactive surface area but also boosts the electron transfer rate reaction compared to other modified electrodes (PAT- and FL-Cu-NDCA MOFs/GCEs). Under the optimized conditions, the modified electrode (AT-Cu-NDCA MOF) exhibited a sharp oxidation peak (+ 0.46 V vs. Ag/AgCl) and higher current response for rutin. The electrode provides a wide linear range from 1 × 10−9 to 50 × 10−6 M, a low detection limit of 1.21 × 10−10 M, LOQ of 0.001 μM, and sensitivity of 0.149 μA μM−1 cm−2. The AT-Cu-NDCA MOF/GC electrode exhibited good stability (RSD = 3.52 ± 0.02% over 8 days of storage), and excellent reproducibility (RSD = 2.62 ± 0.02% (n = 3)). The modified electrode was applied to the determination of rutin in apple, orange, and lemon samples with good recoveries (99.79–99.91, 99.24–99.69, and 99.53–99.83, respectively).

In this study, controlled growth of Ni-MOF was decorated in amino acid-functionalized graphene nanoplatelets (FxGnP) by a solvothermal approach. The synthesized nanocomposite was characterized by various spectral, microscopic, and electrochemical techniques. FE-SEM and TEM image results exhibited the sheet-like structure of FxGnP and spherical-like Ni-MOF with an average size of 5.6 μm. Appreciably, the size of Ni-MOF was reduced to ∼2.3 μm while introducing the FxGnP. The presence of a large number of hydroxyl and epoxy functional groups of FxGnP acts as a nucleation center and restricted the uncontrolled growth of Ni-MOF. The FxGnP-Ni-MOF composite was modified on GCE and then utilized for the oxidation of bisphenol A (BPA). The nanocomposite material showed a sharp peak at +0.38 V vs. Ag/AgCl (saturated NaCl) with a stable response for BPA due to their less particle size with high electroactive surface area and higher electrical conductance, whereas bare GCE failed to the stable determination of BPA. The developed assay for determination of BPA exhibited a wide linear range from 2 × 10−9 M to 10 × 10−6 M, LOD 0.184 × 10−9 M and sensitivity of 247.65 μA mM−1 cm−2. The FxGnP-Ni-MOF/GCE showed good stability and reproducibility against BPA. Finally, the present electrocatalyst was effectively utilized for the quantitative determination of BPA in water samples and obtained results were validated with HPLC method.

There is an urgent need to develop in situ sensors that monitor the continued release of H2S from biological systems to understand H2S-related pathology and pharmacology. For this purpose, we have developed a molybdenum disulfide supported double-layered zinc cobaltite modified carbon cloth electrode (MoS2-ZnCo2O4-ZnCo2O4) based electrocatalytic sensor. The results of our study suggest that the MoS2-ZnCo2O4-ZnCo2O4 electrode has excellent electrocatalytic ability to oxidize H2S at physiological pH, in a minimized overpotential (+0.20 vs. Ag/AgCl) with an amplified current signal. MoS2 grown on double-layered ZnCo2O4 showed relatively better surface properties and electrochemical properties than MoS2 grown on single-layered ZnCo2O4. The sensor delivered excellent analytical parameters, such as low detection limit (5 nM), wide linear range (10 nM-1000 μM), appreciable stability (94.3%) and high selectivity (2.5-fold). The practicality of the method was tested in several major biological fluids. The electrode monitors the dynamics of bacterial H2S in real-time for up to 5 h with good cell viability. Our research shows that MoS2-ZnCo2O4-ZnCo2O4/carbon cloth is a robust and sensitive electrode to understand how bacteria seek to adjust their defense strategies under exogenously induced stress conditions.

In this study, a solution-processing based galvanic deposition approach is described for in-situ deposition of gold nanoparticles (AuNP) on delaminated titanium Ti3C2Tx nanosheets under ultrasonication. The nanocomposite (AuNP@Ti3C2Tx) was placed on a glassy carbon electrode (GCE) and then applied to electrochemically with label-free, and simultaneously sense uric acid (UA), and folic acid (FA) at physiological pH. The modified GCE has attractive figures of merit: (i) The working potentials for UA and AA are well separated (+0.35 V and 0.70 V vs. Ag|AgCl); (ii) wide linear responses (from 0.03–1520 μM for UA and from 0.02–3580 μM for FA; (iii) good electrochemical sensitivities for both UA and FA (0.53 and 0.494 μAμM−1.cm−2, respectively), and (iv) detection limits of 11.5 nM (UA) and 6.20 nM (FA). The electrode exhibited good repeatability (RSD = 4.4%), acceptable reproducibility (RSD = 4.1%), and excellent stability (91.8% over one-month storage). The method was applied to analyze spiked serum samples, and modified GCE is shown appreciable recoveries (97.1–98.8% and 96.8–98.0% for UA, and FA, respectively).

In this study, a solution-processing based galvanic deposition approach is described for in-situ deposition of gold nanoparticles (AuNP) on delaminated titanium Ti

This work was supported by the Ministry of Science and Technology (MOST; 107-2113-M-027-007 – and 108-2221-E-027-063–) Taiwan (ROC) and King Abdullah University of Science and Technology (KAUST), Saudi Arabia.