Surin Saipanya

Cost-effective flow injection amperometric system with metal nanoparticle loaded carbon nanotube modified screen printed carbon electrode for sensitive determination of hydrogen peroxide.

Various metal nanoparticles (NPs) decorated on carbon nanotube (CNT) was modified on the home-made screen printed carbon electrode (SPCE) in order to enhances sensitivity of hydrogen peroxide (H2O2) determination. The simple casting method was used for the electrode modification. The monometallic and bimetallic NPs modified electrodes were investigated for their electrochemical properties for H2O2 reduction. The Pd-CNT/SPCE is appropriated to measure the H2O2 reduction at a potential of -0.3 V, then this modified electrode was incorporated with a home-made flow through cell and applied in a simple flow injection amperometry (FI-Amp). Some parameters influencing the resulted modified electrode and the FI-Amp system were studied. The proposed detection system was able to detect H2O2 in the range of 0.1-1.0 mM, with detection limit of 20 µM. Relative standard deviation for 100 replicated injections of 0.6 mM H2O2 was 2.3%. The reproducibility of 6 electrodes preparing in 3 different lots was 8.2%. It was demonstrated for determination of H2O2 in disinfectant, hair colorant and milk samples. Recoveries in the range of 90-109% were observed. The developed system provided high stability, good repeatability, high sample throughput and low reagent consumption.

An Investigation of a Polydopamine-Graphene Oxide Composite as a Support for an Anode Fuel Cell Catalyst

AbstractHome-made graphene oxide (GO) with a high surface area was functionalized by polydopamine (PDA) and was labeled PDA-GO, while GO without PDA was labeled as GO. With different compositions of metals (Pt and/or Pd), the electrodeposition of the metals onto the prepared GO and PDA-GO supports was prepared for the anode electrocatalyst. The electrocatalytic activities of the electrocatalysts (xPtPd/GO and xPtPd/PDA-GO, where x = 1–5) were studied in the oxidation of alcohols (e.g., methanol and ethanol). Morphologies obtained from transmission electron microscopy (TEM), scanning electron microscopy (SEM), and atomic force microscopy (AFM) images showed that the as-prepared GO and PDA-GO supports can accommodate electrodeposited metals loaded on the topmost layer of the support surfaces, although the size of nanoparticles is somewhat different. The electrochemical results indicated that the xPtPd/PDA-GO catalysts offered outstanding oxidation efficiencies. The prepared 5PtPd/PDA-GO catalyst provided enhanced activity and long-time stability in the oxidation reactions. The GO surface modified by the polymer and the other electrodeposited metal catalysts provided a larger number of available active sites, as the PDA offered a greater electric connection between the metal catalysts and the GO support during alcohol oxidation. Graphical AbstractOptimising ECL Production Through Careful Selection of Co-Reactions Based on Energetics Involved

Electrochemical Deposition of Platinum and Palladium on Gold Nanoparticles Loaded Carbon Nanotube Support for Oxidation Reactions in Fuel Cell

Pt and Pd sequentially electrodeposited Au nanoparticles loaded carbon nanotube (Au-CNT) was prepared for the electrocatalytic study of methanol, ethanol, and formic acid oxidations. All electrochemical measurements were carried out in a three-electrode cell. A platinum wire and Ag/AgCl were used as auxiliary and reference electrodes, respectively. Suspension of the Au-CNT, phosphate buffer, isopropanol, and Nafion was mixed and dropped on glassy carbon as a working electrode. By sequential deposition method, PdPtPt/Au-CNT, PtPdPd/Au-CNT, and PtPdPt/Au-CNT catalysts were prepared. Cyclic voltammograms (CVs) of those catalysts in 1 M H2SO4 solution showed hydrogen adsorption and hydrogen desorption reactions. CV responses for those three catalysts in methanol, ethanol, and formic acid electrooxidations studied in 2 M CH3OH, CH3CH2OH, and HCOOH in 1 M H2SO4 show characteristic oxidation peaks. The oxidation peaks at anodic scan contribute to those organic substance oxidations while the peaks at cathodic scan are related with the reoxidation of the adsorbed carbonaceous species. Comparing all those three catalysts, it can be found that the PdPtPt/Au-CNT catalyst is good at methanol oxidation; the PtPdPt/Au-CNT effectively enhances ethanol oxidation while the PtPdPd/Au-CNT exceptionally catalyzes formic acid oxidation. Therefore, a different stoichiometry affects the electrochemical active surface area of the catalysts to achieve the catalytic oxidation reactions.

Successive electrodeposition of polydopamine and PtPd metal on a graphene oxide support for use as anode fuel cell catalysts

Abstract Successive electropolymerization of dopamine and electrodeposition of Pd and/or Pt on a graphene oxide (GO) support were used to prepare anode catalysts for low-temperature fuel cells. Transmission electron microscopy images were used to investigate the morphologies and distribution of the prepared catalysts, which showed the metal formed as nanoparticles on the catalysts. The GO surface was favorable for the modification with electropolymerized polydopamine (PDA) and the electrodeposition of metal catalyst nanoparticles using a simple preparation process. The PDA-loaded GO composite was used as a matrix for the dispersion of Pt and Pd nanoparticles. GO could be simultaneously modified by PDA and reduced without using reducing agents. The electrocatalytic performance of the catalysts for the oxidation of selected small molecule fuels (e.g., methanol, ethanol and formic acid) was examined. An outstanding catalytic activity and stability was found for the prepared Pt/Pd/PDA/GO composite, which was attributed to the high active surface area.

Preparation and Applications of Precious Metals Adsorbed Activated Carbon Cloth

Precious metal nanoparticles (e.g. Au, Pd and Pt) on activated carbon cloths (ACCs) were simply prepared by impregnation of metal salts dissolving in ethanol solution. Pretreatment of the ACCs was firstly performed in hydrochloric acid solution and nitric acid as oxidizing agent was employed in order to introduce oxygen complex on the ACCs fiber surfaces. Uniformly dispersed metal nanoparticles with diameter of 5-20 nm on the ACC surfaces were simply achieved without using reducing agents. Morphology and composition of the metal adsorbed ACCs were examined by Scanning Electron Microscopy (SEM) and Energy Dispersive Spectroscopy (EDS), respectively. Electrolytic activity of metal/ACCs was investigated by using cyclic voltammetry (CV) to demonstrate the electron-transfer properties. Results demonstrate that metals adsorbed ACCs were easily prepared with simple procedures which will be more convenient for preparations and applications.

Catalytic investigation of PtPd and titanium oxide-loaded reduced graphene oxide for enhanced formic acid electrooxidation

AbstractPreparation, characterization, and electrocatalytic study of the electrodeposited Pt and Pd (e.g., Pt and PtPd) catalysts on titanium dioxide (TiO2) modified reduced graphene oxide (rGO) support for formic acid oxidation were performed. The catalyst composites are labeled as xPt/rGO-TiO2, xPtyPd/rGO-TiO2, and yPd/rGO-TiO2 where x and y are cycle numbers of metal electrodeposition (x and y = 2–6). The characterizations of the catalysts were performed by Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray (EDS), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Small and dispersed metal nanoparticles are obtained on rGO-TiO2. The catalytic performances for formic acid oxidation were measured by cyclic voltammetry (CV) and chronoamperometry (CA). The electrocatalytic results reveal that the bimetallic 4Pt2Pd/rGO-TiO2 catalyst facilitates formic acid oxidations at the lowest potentials and generates the highest oxidation currents and also improves the highest CO oxidation compared to the monometallic 6Pt/rGO-TiO2 catalyst. According to the experimental data, the Pd and TiO2 enhance the electrocatalytic activity of the catalysts towards the formic acid oxidation; the improved catalytic performance of the prepared catalysts strongly relates to the high electrochemically active surface area (ECSA) investigated. Graphical abstractTEM image of xPtyPd/rGO-TiO2 and its CV towards oxidation

Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation

The objective of our work is to improve low-temperature fuel cell catalysts by increasing the surface area to augment the efficiency of catalytic reactions. Reduced graphene oxide (rGO) supports were prepared by adding N-containing derivatives of polydopamine (PDA) and loading of Pt and Pt-based metal alloy nanoparticles were accomplished for catalyst preparation. To study the effects of surface modification on catalyst activity, the GO surfaces modified by addition of PDA (PDA-rGO) were richer in oxygen- and nitrogen-containing functional groups, which reduced the number of graphene defects. Reduction of metals (M = Pt, Pd, PtxPdy where x and y = 1-3) by NaBH4 produced M/GO (metal on GO) and M/PDA-rGO (metal on PDA-rGO) catalysts. Examination of morphology and chemical composition confirmed that the existence of particle size on M/PDA-rGO catalysts was smaller than that on M/GO catalysts in agreement with calculated electrochemically active surface areas (ECSA). Electrochemical analysis was conducted to evaluate the catalyst activity and stability. The prepared catalysts had significantly greater surface areas as a result of association between the metal nanoparticles and the oxygen and nitrogen functional groups on the rGO supports. The catalysts also exhibited lower onset potentials and greater current intensities, If/Ib values, and long-term stabilities for methanol and ethanol oxidation compared with those of commercial PtRu/C. Moreover, the diameter of the Nyquist plot of the catalysts on PDA-rGO were smaller than that of the catalysts M/GO. The results suggest that variation of the PtxPdy atomic ratio on carbon nanocomposites is an encouraging means of enhancing electrocatalytic performance in direct alcohol fuel cell applications.

Sequential injection differential pulse voltammetric method based on screen printed carbon electrode modified with carbon nanotube/Nafion for sensitive determination of paraquat

The screen-printed carbon electrode (SPCE) modified with various nanoparticles has been studied for using as a working electrode in voltammetric technique. The electrochemical behavior of paraquat on different electrodes was studied by cyclic voltammetry (CV), and then differential pulse voltammetry (DPV) has been employed for trace analysis of paraquat based on redox reaction which the peak current was directly proportional to the concentration of paraquat in the solution. The SPCE modified with carbon nanotube dispersed in Nafion and ethanol (SPCE-CNT/Nafion) gave the best result. Sequential injection-differential pulse voltammetric (SI-DPV) method has been developed for more automated analysis and to reduce chemical consumption. The parameters affecting the SI-DPV system such as step potential, modulation amplitude, flow rate, and concentration of sodium chloride as an electrolyte were studied to improve the sensitivity. Under the optimum condition of the system, i.e., Nafion concentration of 1% (w/v), volume of CNT suspension of 2µL, flow rate of 100µLs-1, step potential of 5mV, modulation amplitude of 100mV and concentration of sodium chloride of 1M, a linear calibration graph in the range of 0.54-4.30µM with a good R2 of 0.9955 and a limit of detection of 0.17µM (0.03mgL-1) were achieved. The proposed system shows high tolerance to some possible interfering ions in natural water, surfactant, and other pesticides. The relative standard deviation (RSD) was 4.2% for 11 replicate measurements with the same electrode. The reproducibility for the preparation of 7 modified electrodes was 2.3% RSD. Recoveries of the analysis were obtained in the range of 82-106%. The developed system can be conveniently applied for analysis without pretreatment of the samples.

Determination of PtAuPd metal sequences for electrodeposition on graphene oxide for anode catalyst improvement in methanol oxidation

ABSTRACT The orders of metal deposition (e.g. Pt, Au and Pd) on graphene oxide (GO) and their electrocatalytic properties were investigated. The mono-, bi- and tri-metallic nanoparticles were electrochemically prepared for catalyst preparation. The electrocatalytic activities of the catalysts in 0.5 M CH3OH + 0.5 M H2SO4 solutions were examined. The results showed that the tri-metallic catalysts had higher catalytic activity and stability than the other catalysts. The results indicated that the existing Au and Pd layers before loading of Pt could improve the catalytic activities towards the methanol oxidation.

PtRh@Pt5C/Catalyst Preparation for Methanol Electrooxidation

Bimetallic catalysts PtRh@Pt5/C with different deposit structures were prepared by force deposition followed calcination at 400°C and characterized by cyclic voltammetry (CV) combined with XRD. The activity of the obtained catalysts was examined in methanol electrooxidation by CV. It was found that PtRh@Pt5/C catalysts achieved higher catalytic activity and better tolerance to CO compared with Pt5/C. The surfaces of PtRh@Pt5/C derived from sandwich-like deposit structure was composed of crystallites and amorphous of PtRh alloys, showing exceptional catalytic activity in methanol oxidation with peak potential shifting 0.03V negatively and 90% increase in current density.