Wenyue Gao

Synthesis of Convex Hexoctahedral Palladium@Gold Core–Shell Nanocrystals with {431} High-Index Facets with Remarkable Electrochemiluminescence Activities

Convex hexoctahedral nanocrystals have been synthesized through fast growth kinetics and the use of cetylpyridinium chloride as a capping agent. Monodisperse convex hexoctahedral Pd@Au core-shell nanocrystals with {431} high-index facets are obtained at high reaction rates by using high concentrations of ascorbic acid in the presence of cetylpyridinium chloride. In contrast, octahedral nanocrystals with {111} low-index facets and their {100}-truncated counterparts are formed at low ascorbic acid concentrations. The substitute of cetylpyridinium chloride with cetyltrimethylammonium chloride leads to the generation of concave trisoctahedral Pd@Au core-shell nanocrystals with {331} high-index facets, indicating that cetylpyridinium plays an important role in the formation of convex hexoctahedral nanocrystals. The as-prepared convex hexoctahedral Pd@Au core-shell nanocrystals exhibit remarkable catalytic performances toward electrochemiluminescence compared with truncated octahedral and concave trisoctahedral Pd@Au core-shell nanocrystals.

Ultrasensitive Glutathione Detection Based on Lucigenin Cathodic Electrochemiluminescence in the Presence of MnO2 Nanosheets

Glutathione (GSH) is a crucial antioxidant produced endogenously and plays key roles in biological systems. It is vitally important to design simple, selective, and sensitive methods to sense GSH and monitor changes of GSH concentration. In this work, the cathodic electrochemiluminescence (ECL) of lucigenin in the presence of MnO2 nanosheets at a glassy carbon electrode was utilized for GSH detection. GSH can reduce MnO2 nanosheets into Mn(2+) which can obviously inhibit the ECL of lucigenin. The ECL inhibition efficiencies increase linearly with the concentrations of glutathione in the range of 10 to 2000 nM. The detection limit for GSH measurement is 3.7 nM. This proposed method is highly sensitive, selective, simple, fast, and cost-effective. Moreover, this approach can detect GSH in human serum samples with excellent recoveries, which indicates its promising application under physiological conditions.

Facile surfactant-free synthesis and characterization of Fe3O4@3-aminophenol–formaldehyde core–shell magnetic microspheres

Fe3O4@3-aminophenol–formaldehyde (Fe3O4@APF) core–shell resin polymer magnetic nanocomposites were synthesized using a straightforward surfactant-free methodology. The shell quickly formed within 5 min and could be easily size tunable in the range from 15 to 137 nm by changing the concentrations of 3-aminophenol and formaldehyde. The morphology, composition and magnetic properties of the resulting magnetic microspheres were characterized by scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and thermogravimetric analysis measurements. The magnetic microspheres were uniform in morphology and can be converted into Fe3O4@carbon magnetic nanocomposites because of their excellent thermal stability. Moreover, Fe3O4@APF magnetic microspheres have excelling adsorption properties in the removal of methyl blue.

Facile Synthesis of Porous PtM (M=Cu, Ni) Nanowires and Their Application as Efficient Electrocatalysts for Methanol Electrooxidation

Porous Pt75Cu25 and Pt73Ni27 nanowires were successfully synthesized by a one‐step wet chemical solution method without the use of any template for the first time. The combination of porous and one‐dimensional features and the addition of a second cheap metal offer high catalyst utilization, excellent catalytic activity, and better durability for the methanol oxidation reaction. Porous Pt75Cu25 and Pt73Ni27 nanowires showed mass current densities of 390 (at 0.69) and 503 mA mg−1 (at 0.70 V), respectively. These mass current densities are much higher than that of Pt nanowires (356 mA mg−1 at 0.73 V) and commercial Pt black (195 mA mg−1 at 0.73 V). During the entire 2000 s current–time test, the porous Pt75Cu25 and Pt73Ni27 nanowires also exhibited higher stability for the methanol oxidation reaction than Pt nanowires and commercial Pt black.

Sensitive detection of alkaline phosphatase by switching on gold nanoclusters fluorescence quenched by pyridoxal phosphate

In this work, we designed highly sensitive and selective luminescent detection method for alkaline phosphatase using bovine serum albumin functionalized gold nanoclusters (BSA-AuNCs) as the nanosensor probe and pyridoxal phosphate as the substrate of alkaline phosphatase. We found that pyridoxal phosphate can quench the fluorescence of BSA-AuNCs and pyridoxal has little effect on the fluorescence of BSA-AuNCs. The proposed mechanism of fluorescence quenching by PLP was explored on the basis of data obtained from high-resolution transmission electron microscopy (HRTEM), dynamic light scattering (DLS), UV-vis spectrophotometry, fluorescence spectroscopy, fluorescence decay time measurements and circular dichroism (CD) spectroscopy. Alkaline phosphatase catalyzes the hydrolysis of pyridoxal phosphate to generate pyridoxal, restoring the fluorescence of BSA-AuNCs. Therefore, a recovery type approach has been developed for the sensitive detection of alkaline phosphatase in the range of 1.0-200.0U/L (R2 =0.995) with a detection limit of 0.05U/L. The proposed sensor exhibit excellent selectivity among various enzymes, such as glucose oxidase, lysozyme, trypsin, papain, and pepsin. The present switch-on fluorescence sensing strategy for alkaline phosphatase was successfully applied in human serum plasma with good recoveries (100.60-104.46%), revealing that this nanosensor probe is a promising tool for ALP detection.

Chemiluminescence of creatinine/H2O2/Co2+ and its application for selective creatinine detection

Creatinine is an important biomarker in clinical diagnosis and biomonitoring programs as well as urinary metabolomic/metabonomics research. Current methods are either nonselective, time consuming or require heavy and expensive instruments. In this study, chemiluminescence of creatinine with hydrogen peroxide has been reported for the first time, and its chemiluminescence is remarkably enhanced in the presence of cobalt ions. By utilizing these phenomena, we have developed a sensitive and selective chemiluminescence method for creatinine determination by coupling with flow injection analysis. The calibration curve is linear in the range of 1×10(-7)-3×10(-5)mol/L with a limit of detection (S/N=3) of 7.2×10(-8)mol/L, which is adequate for detecting creatinine in the clinically accepted range. The relative standard deviation for seven measurements of 3×10(-5)mol/L creatinine is 1.2%. The chemiluminescence method was then utilized to detect creatinine in human urine samples after simple dilution with water. It takes less than 1min each measurement and the recoveries for spiked urine samples were 100-103%. The interference study demonstrates that some common species in urine, such as amino acids, ascorbic acid and creatine, have negligible effects on creatinine detection. The present method does not use expensive instruments, enzymes and separation technique. This method has the advantages of sensitivity, selectivity, simplicity, rapidity, and low cost. It holds great promise for basic or comprehensive metabolic panel, drug screening, anti-dopping, and urinary metabolomic/metabonomics research.

Stainless Steel Electrode for Sensitive Luminol Electrochemiluminescent Detection of H2O2, Glucose, and Glucose Oxidase Activity

Electrogenerated chemiluminescence (ECL) application of stainless steel, a robust and cost-effective material, has been developed for the first time. Type 304 stainless steel electrode shows appealing ECL performance in the luminol-H2O2 system. It enables the detection of H2O2 with a linear range from 1 to 1000 nM and a limit of detection of 0.456 nM [signal-to-noise ratio (S/N) = 3]. The ECL method based on type 304 stainless steel electrode is more sensitive, more cost-effective, and much simpler than other ECL methods reported before. Because the stainless steel electrode has excellent performance for H2O2 detection and H2O2 participates in many important enzymatic reactions, applications of stainless steel electrode-based ECL for detection of enzyme activities and enzyme substrates were further investigated by use of glucose oxidase (GODx) and glucose as representative enzyme and substrate. The concentrations of glucose and the activity of GODx were directly proportional to ECL intensities over a range of 0.1-1000 μM and 0.001-0.7 units/mL with limits of detection of 0.076 μM and 0.00087 unit/mL (S/N = 3), respectively. This method was successfully used for determining glucose in honey. Because of their remarkable performance and user-friendly features, stainless steel electrodes hold great promise in various electroanalytical applications, such as biosensing, disposable sensors, and wearable sensors.

A Platinum Highly Concave Cube with one Leg on each Vertex as an Advanced Nanocatalyst for Electrocatalytic Applications

Platinum highly concave cubes with one leg on each vertex (HCCLV) enclosed by {7 5 0} facets were conveniently synthesized for the first time through a one‐pot solvothermal method in a mixed solvent of oleylamine and isopropanol containing platinum(II) acetylacetonate. This method can also be extended to the synthesis of Pt dendrite nanocubes at shorter reaction times. Preferential overgrowth may facilitate the formation of Pt HCCLV in the presence of oleylamine and isopropanol. The Pt HCCLV exhibit excellent electrocatalytic activity for the oxidation of methanol (7.76×) and ethanol (5.46×) compared to commercial Pt black. Furthermore, the Pt HCCLV show higher stability than Pt dendrite nanocubes and commercial Pt black. The Pt HCCLV also remarkably improve the electrochemiluminescence activity of the luminol/H2O2 system.

Wireless Electrochemiluminescence with Disposable Minidevice

Wireless electrochemiluminescence system based on the wireless energy transmission technique has been demonstrated for the first time. It has a disposable transmitter and a coiled energy receptor. The coiled energy receptor is smartly used as the electrode. The wireless electrochemiluminescence system has been used to detect hydrogen peroxide with good sensitivity, featuring advantages of easy manipulation, low cost, and small size. The handy and cheap wireless electrochemiluminescence device can use laptops as a power supply. It is promising for the development of portable or disposable electrochemiluminescence devices for various applications (e.g., such as point of care testing, field analysis, scientific research, and chemical education). These advantages enable one to integrate many wireless electrochemiluminescence minidevices with screen printing coiled electrode arrays in microwell plates and charge-coupled devices (CCD) cameras to develop electrochemiluminescence high-throughput screening systems with broad applications in clinical analysis, drug screening, and biomolecular interaction studies.

Large refrigerant capacity of RGa (R = Tb and Dy) compounds

The magnetic properties and magnetocaloric effects (MCEs) of RGa (R = Tb and Dy) compounds are investigated. The TbGa compound exhibits two successive magnetic transitions: spin-reorientation (SR) transition at TSR = 31 K and second-order ferromagnetic (FM)–paramagnetic (PM) transition at Curie temperature TC = 154 K, while the DyGa compound undergoes a SR transition with TSR=25 K and a FM–PM transition with TC = 113 K. It is noteworthy that a broad distribution of the magnetic entropy change peak is observed. The values of the refrigerant capacity (RC) for TbGa and DyGa are found to be 620.6 and 381.9 J/kg for a field change of 0–5 T, respectively. And for a field change of 0–7 T, the values are 900 and 584.2 J/kg, respectively. The large value of RC for TbGa and DyGa originates from the combined contribution from SR and FM–PM transitions, which enlarges the temperature span of large MCE.