Colorimetric and Electrochemical Dual-Mode Detection of Thioredoxin 1 Based on the Efficient Peroxidase-Mimicking and Electrocatalytic Property of Prussian Blue Nanoparticles.

As a potent detection method for cancer biomarkers in physiological fluid, a colorimetric and electrochemical dual-mode sensing platform for breast cancer biomarker thioredoxin 1 (TRX1) was developed based on the excellent peroxidase-mimicking and electrocatalytic property of Prussian blue nanoparticles (PBNPs). PBNPs were hydrothermally synthesized using K3[Fe(CN)6] as a precursor and polyvinylpyrrolidone (PVP) as a capping agent. The synthesized spherical PBNPs showed a significant peroxidase-like activity, having approximately 20 and 60% lower Km values for 3,3',5,5'-tetramethylbenzidine (TMB) and H2O2, respectively, compared to those of horseradish peroxidase (HRP). The PBNPs also enhanced the electron transfer on the electrode surface. Based on the beneficial features, PBNPs were used to detect target TRX1 via sandwich-type immunoassay procedures. Using the strategies, TRX1 was selectively and sensitively detected, yielding limit of detection (LOD) values as low as 9.0 and 6.5 ng mL-1 via colorimetric and electrochemical approaches, respectively, with a linear range of 10-50 ng mL-1 in both strategies. The PBNP-based TRX1 immunoassays also exhibited a high degree of precision when applied to real human serum samples, demonstrating significant potentials to replace conventional HRP-based immunoassay systems into rapid, robust, reliable, and convenient dual-mode assay systems which can be widely utilized for the identification of important target molecules including cancer biomarkers.

Highly Conductive Peroxidase-like Ce-MoS2 Nanoflowers for the Simultaneous Electrochemical Detection of Dopamine and Epinephrine.

The accurate and simultaneous detection of neurotransmitters, such as dopamine (DA) and epinephrine (EP), is of paramount importance in clinical diagnostic fields. Herein, we developed cerium-molybdenum disulfide nanoflowers (Ce-MoS2 NFs) using a simple one-pot hydrothermal method and demonstrated that they are highly conductive and exhibit significant peroxidase-mimicking activity, which was applied for the simultaneous electrochemical detection of DA and EP. Ce-MoS2 NFs showed a unique structure, comprising MoS2 NFs with divalent Ce ions. This structural design imparted a significantly enlarged surface area of 220.5 m2 g-1 with abundant active sites as well as enhanced redox properties, facilitating electron transfer and peroxidase-like catalytic action compared with bare MoS2 NFs without Ce incorporation. Based on these beneficial features, Ce-MoS2 NFs were incorporated onto a screen-printed electrode (Ce-MoS2 NFs/SPE), enabling the electrochemical detection of H2O2 based on their peroxidase-like activity. Ce-MoS2 NFs/SPE biosensors also showed distinct electrocatalytic oxidation characteristics for DA and EP, consequently yielding the highly selective, sensitive, and simultaneous detection of target DA and EP. Dynamic linear ranges for both DA and EP were determined to be 0.05~100 µM, with detection limits (S/N = 3) of 28 nM and 44 nM, respectively. This study shows the potential of hierarchically structured Ce-incorporated MoS2 NFs to enhance the detection performances of electrochemical biosensors, thus enabling extensive applications in healthcare, diagnostics, and environmental monitoring.

Ni-Co bimetallic decorated dodecahedral ZIF as an efficient catalyst for photoelectrochemical degradation of sulfamethoxazole coupled with hydrogen production.

In this work, a NiCo bimetallic ZIF (BMZIF) dodecahedron material has been synthesized by the precipitation approach and then used for simultaneously photoelectrocatalytic degradation of sulfamethoxazole (SMX) and hydrogen production. The combination of Ni/Co loading in ZIF structure increased the specific surface area 1484 (m2 g-1) and photocurrent density (0.4 mA cm-2), which can facilitate the good charge transfer efficiency. In presence of peroxymonosulfate (PMS, 0.1 mM), the complete degradation of SMX (10 mg L-1) was achieved at initial pH of 7 within 24 min, with the pseudo-first-order rate constants of 0.18 min-1 and TOC removal efficiency of 85 %. Radical scavenger experiments affirm that •OH radicals were the primary oxygen reactive species to drive the SMX degradation. Along with SMX degradation at the anode, the H2 production was observed at the cathode (140 µmol cm-2 h-1), which was 1.5 and 3 times higher than that of Co-ZIF and Ni-ZIF, respectively. The superior catalytic performance of BMZIF was assigned to the distinctive internal structure and synergistic effect between ZIF and Ni/Co bimetals, which improves light absorption and charge conduction efficiency. This study may provide insight into the new way to treat polluted water and simultaneously produce green energy using bimetallic ZIF in a PEC system.

Investigation of carbonaceous materials electrosorption attributes and its performance for capacitive deionization process within the presence of humic acid.

This present investigation emphasizes on pros and cons of humic acid (HA) on electrosorption behaviour and performance efficiency of capacitive deionization (CDI) process. Electrosorptive removal of HA was examined by lab scale CDI flow cell under 100 ppm Na2SO4 as a supporting electrolyte. In addition, the electrosorption capacitance and desalination performances were also evaluated through cyclic voltammetry studies. In this perspective, we employed the carbon-based electrodes such as chemically treated activated carbon cloth (ACC), carbon aerogel electrodes grade-I (CA-I) and carbon aerogel electrode grade-II (CA-II) with active surface area for 1 cm2 and 24 cm2 respectively. The specific capacitance values of 30, 23 and 10 F g-1 were achieved for ACC, CA-1 and CA-II with 100 ppm Na2SO4 and 10 ppm HA electrolyte solution. The experimental results substantiated that ACC electrode exhibited higher removal efficiency compared to other two carbon electrodes (CA-I and CA-II). Eventually, the electrosorption removal of natural organic matter HA was observed as 15% for CA-I, 30% for CA-II and 58% for ACC electrodes in a CDI flow cell.

Fe/Ni Bimetallic Organic Framework Deposited on TiO2 Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction.

Photoelectrochemical (PEC) water splitting is a promising strategy to improve the efficiency of oxygen evolution reactions (OERs). However, the efficient adsorption of visible light as well as long-term stability of light-harvesting electrocatalysis is the crucial issue in PEC cells. Metal-organic framework (MOF)-derived bimetallic electrocatalysis with its superior performance has wide application prospects in OER and PEC applications. Herein, we have fabricated a nickel and iron bimetallic organic framework (FeNi-MOF) deposited on top of anodized TiO2 nanotube arrays (TNTA) for PEC and OER applications. The FeNi-MOF/TNTA was incorporated through the electrochemical deposition of Ni2+ and Fe3+ onto the surface of TNTA and then connected with organic ligands by the hydrothermal transformation. Therefore, FeNi-MOF/TNTA demonstrates abundant photoelectrocatalytic active sites that can enhance the photocurrent up to 1.91 mA/cm2 under 100 mW/cm2 and a negligible loss in activity after 180 min of photoreaction. The FeNi-MOF-doped photoanode shows predominant photoelectrochemical performance due to the boosted excellent light-harvesting ability, rapid photoresponse, and stimulated interfacial energy of charge separation under the UV-visible light irradiation conditions. The results of this study give deep insight into MOF-derived bimetallic nanomaterial synthesis for photoelectrochemical OER and provide guidance on future electrocatalysis design.

Experimental and Theoretical Studies on a Simple S-S-Bridged Dimeric Schiff Base: Selective Chromo-Fluorogenic Chemosensor for Nanomolar Detection of Fe2+ & Al3+ Ions and Its Varied Applications.

A simple S-S (disulfide)-bridged dimeric Schiff base probe, L, has been designed, synthesized, and successfully characterized for the specific recognition of Al3+ and Fe2+ ions as fluorometric and colorimetric "turn-on" responses in a dimethylformamide (DMF)-H2O solvent mixture, respectively. The probe L and each metal ion bind through a 1:1 complex stoichiometry, and the plausible sensing mechanism is proposed based on the inhibition of the photoinduced electron transfer process (PET). The reversible chemosensor L showed high sensitivity toward Al3+ and Fe2+ ions, which was analyzed by fluorescence and UV-vis spectroscopy techniques up to nanomolar detection limits, 38.26 × 10-9 and 17.54 × 10-9 M, respectively. These experimental details were advocated by density functional theory (DFT) calculations. The practical utility of the chemosensor L was further demonstrated in electrochemical sensing, in vitro antimicrobial activity, molecular logic gate function, and quantification of the trace amount of Al3+ and Fe2+ ions in real water samples.

Improved electrocatalytic activity of Au@Fe3O4 magnetic nanoparticles for sensitive dopamine detection.

Substantially, noble metals are important for the development of low-cost, sensitive, selective, superior performance, and portable electrochemical sensors. Herein, we describe gold (Au) nanoparticles (NPs) systematically decorated with magnetic Fe3O4 nanocomposites on the fabrication of sensitive dopamine sensor is described. Magnetic Au@Fe3O4 nanocomposites were prepared by reducing HAuCl4 on the surfaces of Fe3O4 nanoparticles. The surface morphology of Au@Fe3O4 nanocomposites was characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical behaviour of the modified electrode was investigated by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and amperometric techniques, in which it was shown to be highly sensitive and selective towards DA. The amperometric detection of dopamine sensor, using this sensing element, exhibits a wide linear response of 0-0.8 µM with a low detection limit of 2.7 nM. In addition, the fabricated electrode showed an excellent stability and good reproducibility. The proposed analytical method was successfully applied to determine the concentration of dopamine in human urine samples and the unknown concentration of DA in human urine samples No. 1, 2 and 3 were determined as 0.056 ± 0.82 × 10-3, 0.037 ± 0.87 × 10-3 and 0.020 ± 0.94 × 10-3 µM, respectively, with recoveries ranging from 97.2% to 103.4%, suggesting that the fabricated electrode can effectively detect DA in human urine samples.