In this work, silver nanoparticles decorated onto polyaniline nanowires were synthesized site-specifically onto Pt working electrodes (with only 0.8 mm2 area) using a novel, rapid, and effective electrochemical procedure: electropolymerization of PANi NWs and electrodeposition of AgNPs. The complementary properties of PANi NWs and AgNPs were obtained, including high surface area, high electrochemical activity, high biocompatibility, high chemical stability and good adhesion with the electrode surface. Obtained results showed advantages of the electrosynthesis method compared to traditional methods, which have difficulties in binding between modifying materials with electrode surfaces. The sensor surface modification with the PANi NWs/AgNPs material facilitated the probe DNA immobilization and improved the electrochemical signal of the DNA sensors. The detection limit of the sensors was 2.80 × 10−15 M. The DNA sensors exhibited advantages including direct detection, high sensitivity, good specificity, and potential miniaturization for development of lab-on-a-chip systems.
A metal-organic framework MIL-53(Fe) was successfully synthesized by a simple hydrothermal method. A synthesized MIL-53(Fe) sample was characterized, and results indicated that the formed MIL-53(Fe) was a single phase with small particle size of 0.8 μm and homogeneous particle size distribution was obtained. The synthesized MIL-53(Fe) has been used to modify a glassy carbon electrode (GCE) by a drop-casting technique. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements of the MIL-53(Fe)-modified GCE showed that the MIL-53(Fe) was successfully immobilized onto the GCE electrode surface and the electrochemical behavior of the GCE/MIL-53(Fe) electrode was stable. In addition, several electrochemical parameters of MIL-53(Fe)-modified GCE (GCE/MIL-53(Fe)) including the heterogeneous standard rate constant (
k
0
) and the electrochemically effective surface area (
A
) were calculated. Obtained results demonstrated that the synthesized MIL-53(Fe) with the small particle size, highly homogeneous particle size, and high electrochemically effective surface area was able to significantly enhance the electrochemical response signal of the working electrode. Therefore, the GCE/MIL-53(Fe) electrode has been used as a highly sensitive electrochemical sensor for cadmium ion (Cd(II)) monitoring in aqueous solution using differential pulse voltammetry (DPV) technique. The response signal of the electrochemical sensor increased linearly in the Cd(II) ion concentration range from 150 nM to 450 nM with the limit of detection (LOD) of 16 nM.
Nanostructured cathode materials based on Mn-doped olivine LiMnxFe1−xPO4 (x = 0, 0.1, 0.2, and 0.3) were successfully synthesized via a hydrothermal route. The field-emission scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS) analyzed results indicated that the synthesized LiMnxFe1−xPO4 (x = 0, 0.1, 0.2, and 0.3) samples possessed a sphere-like nanostructure and a relatively homogeneous size distribution in the range of 100–200 nm. Electrochemical experiments and analysis showed that the Mn doping increased the redox potential and boosted the capacity. While the undoped olivine (LiFePO4) had a capacity of 169 mAh g−1 with a slight reduction (10%) in the initial capacity after 50 cycles (150 mAh g−1), the Mn-doped olivine samples (LiMnxFe1−xPO4) demonstrated reliable cycling tests with negligible capacity loss, reaching 151, 147, and 157 mAh g−1 for x = 0.1, 0.2, and 0.3, respectively. The results from electrochemical impedance spectroscopy (EIS) accompanied by the galvanostatic intermittent titration technique (GITT) have resulted that the Mn substitution for Fe promoted the charge transfer process and hence the rapid Li transport. These findings indicate that the LiMnxFe1−xPO4 nanostructures are promising cathode materials for lithium ion battery applications.
A novel nanostructured material based on ERGO/PANi NWs/AgNFs was electrosynthesized on a Pt microelectrode and was used for the first time to develop an electrochemical DNA sensor.
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