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Platinum particles supported on mesoporous carbons: fabrication and electrocatalytic performance in methanol-tolerant oxygen-reduction reactions.

ABSTRACT: In this report, we describe the preparation and electrochemical characterization of a Pt electrocatalyst, which was synthesized from hexachloroplatinic acid, using the incipient wetness impregnation method. This carbon mesoporous materials (Pt-CMMs) electrocatalyst was used for catalyzing the oxidation of methanol and its oxygen-reduction reaction. The electrocatalytic oxidation of methanol was studied using linear-sweep voltammograms (LSV), polarization and chronoamperometric measurements. Phase characterizations and morphological analyses were performed using 3D excitation-emission fluorescent matrix (EEFM) spectroscopy, UV-Vis absorption measurements, and X-ray diffraction (XRD) and environmental scanning electron microscopy (ESEM) techniques; the ESEM system was equipped with an energy-dispersive spectrometer (EDS). The oxidation capacity measured using a LSV might explain the high activity exhibited by the Pt-CMM electrocatalysts in methanol-tolerant oxygen reduction, and the results demonstrated that the potential and current density of the main reaction peak of the Pt-CMMs electrocatalyst changed during the reaction. Moreover, EEFM spectroscopy and XRD were determined to be appropriate and effective methods for characterizing Pt clusters that enhance their intrinsic emission from Pt-CMMs electrocatalysts in electrocatalytic-treatment systems. Furthermore, the ESEM-EDS results showed that fresh Pt nanoparticles were highly dispersed on CMMs and featured a 20 nm diameter and a narrow particle-size distribution.

SUBMITTER: Dong CD

PROVIDER: S-EPMC4148669 | biostudies-other | 2014

REPOSITORIES: biostudies-other

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Project description:Herein, we demonstrated that carbon-supported platinum (Pt/C) is a low-cost and high-performance electrocatalyst for polymer electrolyte fuel cells (PEFCs). The ethanol reduction method was used to prepare the Pt/C catalyst, which was realized by an effective matching of the carbon support and optimization of the Pt content for preparing a membrane electrode assembly (MEA). For this, the synthesis of Pt/C catalysts with different Pt loadings was performed on two different carbons (KB1600 and KB800) as new support materials. Analysis of the XRD pattern and TEM images showed that the Pt nanoparticles (NPs) with an average diameter of ca. 1.5 nm were uniformly dispersed on the carbon surface. To further confirm the size of the NPs, the coordination numbers of Pt derived from X-ray absorption fine structure (XAFS) data were used. These results suggest that the NP size is almost identical, irrespective of Pt loading. Nitrogen adsorption-desorption analysis indicated the presence of mesopores in each carbon. The BET surface area was found to increase with increasing Pt loading, and the value of the BET surface area was as high as 1286 m2 gcarbon -1. However, after 40 wt% Pt loading on both carbons, the BET surface area was decreased due to pore blockage by Pt NPs. The oxidation reduction reaction (ORR) activity for Pt/KB1600, Pt/KB800 and commercial Pt/C was evaluated by Koutecky-Levich (K-L) analysis, and the results showed first-order kinetics with ORR. The favourable surface properties of carbon produced Pt NPs with increased density, uniformity and small size, which led to a higher electrochemical surface area (ECSA). The ECSA value of the 35 wt% Pt/KB1600 catalyst was 155.0 m2 gpt -1 higher than that of the Pt/KB800 and commercial Pt/C (36.7 wt%) catalysts. A Higher ECSA indicates more available active sites for catalyst particles. The single cell test with MEA revealed that the cell voltage in the high current density regions depends on the BET surface area, and the durability of the 35 wt% Pt/KB1600 catalyst was superior to that of the 30 wt% Pt/KB800 and commercial Pt/C (46.2 wt%) catalysts. This suggests that an optimal ratio of Pt to Pt/KB1600 catalyst provides adequate reaction sites and mass transport, which is crucial to the PEFC's high performance.

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Platinum particles supported on mesoporous carbons: fabrication and electrocatalytic performance in methanol-tolerant oxygen-reduction reactions.

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