Manganese Oxide Carbon-Based Nanocomposite in Energy Storage Applications

Global increasing demand in the need of energy leads to the development of non-conventional, high power energy sources. Supercapacitors (SCs) are one of the typical non-conventional energy storage devices which are based on the principle of electrochemical energy conversion. SCs are promising energy storage devices for better future energy technology. Increasing progress has been made in the development of applied and fundamental aspects of SCs. Manganese oxide electrode materials have been well studied; however, their capacitive performance is still inadequate for practical applications. Recent research is mainly focused on enhancing manganese oxide capacitive performance through the incorporation of electrically conductive materials and by controlling its morphology to reveal a more active surface area for redox reactions. In this review, progress in the applications of manganese oxide carbon-based materials towards the development of highly effective SCs is briefly discussed. In this regard, manganese oxide carbon-based nanocomposites synthesis methods and techniques used to approximate the capacitance of electrode materials are discussed

Layered Xerogel Films Incorporating Monolayer Protected Cluster Networks on Platinum Black Modified Electrodes for Enhanced Sensitivity in 1st Generation Uric Acid Biosensing

Amperometric uric acid (UA) biosensing schemes incorporating networks of alkanethiolate‐protected gold nanoparticles, monolayer protected clusters (MPCs), and platinum black (Pt‐B) electrode modification through the layer‐by‐layer construction of xerogels are investigated. MPC doping and Pt‐B augmentation are implemented within hydroxymethyltriethoxysilane xerogel bilayers at platinum electrodes. The first xerogel adlayer is doped with an MPC network and houses uricase for the enzymatic reaction required for first‐generation schemes. Polyluminol–aniline and polyurethane are used as selective/stabilizing interfacial layers. The sensing performance with and without Pt‐B and/or MPC doping is assessed by amperometry with standardized UA injections. The use of each individual material results in an enhancement of UA sensitivity compared with analogous films without these materials. The use of Pt‐B and MPC doping in concert results in a biosensor design with the highest observed UA sensitivity (0.97 μA mm−1) and fast, linear responses over physiologically relevant UA concentrations. Enhancement is attributed to Pt‐B providing increased electrode surface area and integration into the xerogel for greater electronic coupling of the MPC network and more efficient reporting of H2O2 oxidation. The findings have implications for advancing clinical in vivo sensing devices that require scalability or additional biocompatibility layering, both of which would benefit from signal enhancement strategies

Enzyme–free uric acid electrochemical sensors using β–cyclodextrin modified carboxylic acid functionalized carbon nanotubes

Carboxylic acid-functionalized multi-walled carbon nanotubes (COOH-MWCNT) were modified via ultrasonication with β-cyclodextrin (β-CD) to obtain a COOH-MWCNT:β-CD nanocomposite material for the purpose of developing an enzyme-free electrochemical sensor for uric acid—a clinically relevant molecule implemented in pregnancy-induced hypertension diagnosis. The nanocomposite material is deposited onto glassy carbon electrodes and subsequently capped with layers of Nafion and Hydrothane polyurethane. The surface morphology and electronic structure of the nanocomposite material were characterized using UV–Vis, TEM, and FTIR. The performance of the electrochemical sensor was measured through direct injection of UA during amperometry. With the high surface area of the COOH-MWCNT in concert with the selectivity provided by β-CD, the composite system outperforms similar COOH-MWCNT systems, displaying enhanced UA sensitivity versus films with only COOH-MWCNT. With the improved sensitivity (4.28 ± 0.11 µA mM−1) and fast response time (4.0 ± 0.5 s), the sensors offer wide detection of UA across clinically relevant ranges (100–700 μM) as well as demonstrated selectivity against various interferents

Functionalized Carbon Nanotube Adsorption Interfaces for Electron Transfer Studies of Galactose Oxidase

Modified electrodes featuring specific adsorption platforms able to access the electrochemistry of the copper containing enzyme galactose oxidase (GaOx) were explored, including interfaces featuring nanomaterials such as nanoparticles and carbon nanotubes (CNTs). Electrodes modified with various self-assembled monolayers (SAMs) including those with attached nanoparticles or amide-coupled functionalized CNTs were examined for their ability to effectively immobilize GaOx and study the redox activity related to its copper core. While stable GaOx electrochemistry has been notoriously difficult to achieve at modified electrodes, strategically designed functionalized CNT-based interfaces, cysteamine SAM-modified electrode subsequently amide-coupled to carboxylic acid functionalized single wall CNTs, were significantly more effective with high GaOx surface adsorption along with well-defined, more reversible, stable (≥ 8 days) voltammetry and an average ET rate constant of 0.74 s-1 in spite of increased ET distance - a result attributed to effective electronic coupling at the GaOx active site. Both amperometric and fluorescence assay results suggest embedded GaOx remains active. Fundamental ET properties of GaOx may be relevant to biosensor development targeting galactosemia while the use functionalized CNT platforms for adsorption/electrochemistry of electroactive enzymes/proteins may present an approach for fundamental protein electrochemistry and their future use in both direct and indirect biosensor schemes

First Generation Amperometric Biosensing of Galactose with Xerogel-Carbon Nanotube Layer-By-Layer Assemblies

A first-generation amperometric galactose biosensor has been systematically developed utilizing layer-by-layer (LbL) construction of xerogels, polymers, and carbon nanotubes toward a greater fundamental understanding of sensor design with these materials and the potential development of a more efficient galactosemia diagnostic tool for clinical application. The effect of several parameters (xerogel silane precursor, buffer pH, enzyme concentration, drying time and the inclusion of a polyurethane (PU) outer layer) on galactose sensitivity were investigated with the critical nature of xerogel selection being demonstrated. Xerogels formed from silanes with medium, aliphatic side chains were shown to exhibit significant enhancements in sensitivity with the addition of PU due to decreased enzyme leaching. Semi-permeable membranes of diaminobenzene and resorcinol copolymer and Nafion were used for selective discrimination against interferent species and the accompanying loss of sensitivity with adding layers was countered using functionalized, single-walled carbon nanotubes (CNTs). Optimized sensor performance included effective galactose sensitivity (0.037 μA/mM) across a useful diagnostic concentration range (0.5 mM to 7 mM), fast response time (~30 s), and low limits of detection (~80 μM) comparable to literature reports on galactose sensors. Additional modification with anionic polymer layers and/or nanoparticles allowed for galactose detection in blood serum samples and additional selectivity effectiveness

Morphology of hydrothermally synthesized ZnO nanoparticles tethered to carbon nanotubes affects electrocatalytic activity for H 2 O 2 detection

We describe the synthesis of zinc oxide (ZnO) nanoparticles and demonstrate their attachment to multiwalled carbon tubes, resulting in a composite with a unique synergistic effect. Morphology and size of ZnO nanostructures were controlled using hydrothermal synthesis, varying the hydrothermal treatment temperature, prior to attachment to carboxylic acid functionalized multi-walled carbon nanotubes for sensing applications. A strong dependence of electrocatalytic activity on nanosized ZnO shape was shown. High activity for H2O2 reduction was achieved when nanocomposite precursors with a roughly semi-spherical morphology (no needle-like particles present) formed at 90 °C. A 2.4-fold increase in cyclic voltammetry current accompanied by decrease in overpotential from the composites made from the nanosized, needle-like-free ZnO shapes was observed as compared to those composites produced from needle-like shaped ZnO. Electrocatalytic activity varied with pH, maximizing at pH 7.4. A stable, linear response for H2O2 concentrations was observed in the 1 “20 mM concentration range

Characterization of Hydrothermally Synthesized Zinc Oxide (ZnO) Nanoparticles

Zinc oxide (ZnO) is a chemically and thermally stable n-type semiconducting material with extremely high sensitivity to combustible and reducing gases and has therefore been successfully used as a transducer in gas sensing, chemical and biological, photovoltaic, piezoelectric and fuel cell devices. To optimize ZnO conducting/semi-conducting properties for these applications, we seek to control the size distribution and morphology while fabricating the nanostructures. We have hydrothermally synthesized ZnO nanoparticles at low temperatures, varying the temperature between 40-90°C. A critical morphology change was observed at ca. 60°C. Control of the ratio of rod-like to nanoparticle-like shapes (30-70 nm diam.) along with mean diam., affecting sensing properties, can be achieved via temperature control during the ZnO synthesis

Morphology of Hydrothermally Synthesized ZnO Nanoparticles Tethered to Carbon Nanotubes Affects Electrocatalytic Activity For H₂O₂ Detection

We describe the synthesis of zinc oxide (ZnO) nanoparticles and demonstrate their attachment to multiwalled carbon tubes, resulting in a composite with a unique synergistic effect. Morphology and size of ZnO nanostructures were controlled using hydrothermal synthesis, varying the hydrothermal treatment temperature, prior to attachment to carboxylic acid functionalized multi-walled carbon nanotubes for sensing applications. A strong dependence of electrocatalytic activity on nanosized ZnO shape was shown. High activity for H2O2 reduction was achieved when nanocomposite precursors with a roughly semi-spherical morphology (no needle-like particles present) formed at 90 °C. A 2.4-fold increase in cyclic voltammetry current accompanied by decrease in overpotential from the composites made from the nanosized, needle-like-free ZnO shapes was observed as compared to those composites produced from needle-like shaped ZnO. Electrocatalytic activity varied with pH, maximizing at pH 7.4. A stable, linear response for H 2O2 concentrations was observed in the 1-20 mM concentration range