Abstract:Modified Pt and Ti substrates were prepared by electrodeposition of nanocrystallite Pt and Pt x -Sn y catalysts for electro-oxidation of ethanol, 1-propanol and 2-propanol. The chemical composition, the phase structure and the surface morphology of the Pt and Pt x -Sn y electrodeposits were studied by X-ray diffractometer (XRD), energy dispersive X-ray spectroscopy (EDX) and scanning electron microscope (SEM). Their electro-catalytic activities were studied in 0.5 M H 2 SO 4 by cyclic votlammetry and chronoamp… Show more
“…Generally, the Tafel slope provides insights into whether the rds involves the transfer of the first or second electron and whether a chemical reaction is involved [51]. The Tafel slope values were close to the theoretical value of 120 mV dec -1 obtained on carbon-supported Pt catalysts, consistent with a Temkin-type adsorption mechanism for both OHads and ethoxy adsorption at low potentials [52,53].…”
In this study, we synthesized Pt-Rh nanowires (NWs) through chemical reduction of metallic precursors using formic acid at room temperature, excluding the use of surfactants, templates, or stabilizing agents. These NWs were supported on two substrates: carbon (Vulcan XC-72R) and carbon modified with tin oxide (SnO<sub>2</sub>) via the sol-gel method (10 wt.% SnO<sub>2</sub>). We explored the electroactivity of Pt/SnO<sub>2</sub>/C, Pt-Rh/C, Pt-Rh/SnO<sub>2(commercial)</sub>/C (commercial SnO<sub>2</sub>), and Pt-Rh/SnO<sub>2</sub>/C NWs toward electrochemical oxidation of ethanol in acidic media using various techniques, including CO-stripping, cyclic voltammetry, derivative voltammetry, chronoamperometry, and steady-state polarization curves. Physical characterization involved X-ray diffraction and transmission electron microscopy. The synthesized NWs exhibit higher ethanol oxidation activity than the commercial Pt/C (Johnson Matthey™) catalyst. Rh atoms are hypothesized to enhance complete ethanol oxidation, while the NW morphology improves ethanol adsorption at the catalyst surface for subsequent oxidation. Additionally, the choice of support material plays a significant role in influencing the catalytic activity. The superior catalytic activity of Pt-Rh/SnO<sub>2</sub>/C NWs may be attributed to the facile dissociation of the C-C bond, low CO adsorption (electronic effect due to Rh presence), and the bifunctional mechanism facilitated by the oxophilic nature of the SnO<sub>2</sub> support.
“…Generally, the Tafel slope provides insights into whether the rds involves the transfer of the first or second electron and whether a chemical reaction is involved [51]. The Tafel slope values were close to the theoretical value of 120 mV dec -1 obtained on carbon-supported Pt catalysts, consistent with a Temkin-type adsorption mechanism for both OHads and ethoxy adsorption at low potentials [52,53].…”
In this study, we synthesized Pt-Rh nanowires (NWs) through chemical reduction of metallic precursors using formic acid at room temperature, excluding the use of surfactants, templates, or stabilizing agents. These NWs were supported on two substrates: carbon (Vulcan XC-72R) and carbon modified with tin oxide (SnO<sub>2</sub>) via the sol-gel method (10 wt.% SnO<sub>2</sub>). We explored the electroactivity of Pt/SnO<sub>2</sub>/C, Pt-Rh/C, Pt-Rh/SnO<sub>2(commercial)</sub>/C (commercial SnO<sub>2</sub>), and Pt-Rh/SnO<sub>2</sub>/C NWs toward electrochemical oxidation of ethanol in acidic media using various techniques, including CO-stripping, cyclic voltammetry, derivative voltammetry, chronoamperometry, and steady-state polarization curves. Physical characterization involved X-ray diffraction and transmission electron microscopy. The synthesized NWs exhibit higher ethanol oxidation activity than the commercial Pt/C (Johnson Matthey™) catalyst. Rh atoms are hypothesized to enhance complete ethanol oxidation, while the NW morphology improves ethanol adsorption at the catalyst surface for subsequent oxidation. Additionally, the choice of support material plays a significant role in influencing the catalytic activity. The superior catalytic activity of Pt-Rh/SnO<sub>2</sub>/C NWs may be attributed to the facile dissociation of the C-C bond, low CO adsorption (electronic effect due to Rh presence), and the bifunctional mechanism facilitated by the oxophilic nature of the SnO<sub>2</sub> support.
“…Tafel slopes around 120 mV dec -1 have been obtained on single-crystal carbon-supported Pt catalysts. Generally, the Tafel slope allows the observation of whether the rds is the transfer of the first or second electron and if a chemical reaction is involved [46]. Thus, for the synthesised Pt/C NWs catalyst, the obtained slope value (close to 120.0 mV dec -1 ) is in agreement with a mechanism that involves Temkin-type adsorption for both OH ads and ethoxy at low potentials [47].…”
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“…Some work has been done to investigate the electrooxidation of isopropanol on Pt-based catalysts in alkaline medium [9,10]. However, Pt has a low activity for isopropanol electrooxidation.…”
Abstract:The diffusion coefficient of isopropanol in alkaline medium using electrochemical methods on Pd electrode has been studied by linear sweep voltammetry (LSV) with different sweep rate and chronoamperometry in 1.0 M KOH solution containing 1.0 M isopropanol. Isopropanol oxidation on the Pd electrode is an irreversible charge-transport process and controlled by a diffusion process. The diffusion coefficient of isopropanol on the Pd electrode is obtained as 1.01 10 -6 cm 2 s -1 using the LSV method and 1.06 10 -6 cm 2 s -1 using the chronoamperometry method. The average diffusion coefficient of isopropanol is 1.04 10 -6 cm 2 s -1 .
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