Electro-oxidation of formic acid catalyzed by FePt nanoparticles

文献情報

出版日 2006-05-25
DOI 10.1039/B603045A
インパクトファクター 3.676
著者

Wei Chen, Jaemin Kim, Shouheng Sun, Shaowei Chen


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要旨

The electrocatalytic oxidation of formic acid at a gold electrode functionalized with FePt nanoparticles was studied by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) in a mixed solution of 0.1 M HCOOH and 0.1 M HClO4. The FePt bimetallic nanoparticles, with a mean diameter of 3 nm, were prepared by a chemical reduction method. The Au/FePt nanostructured electrode was prepared firstly by the deposition of FePt nanoparticles onto a clean Au electrode surface, followed by ultraviolet ozone treatment to remove the organic coating. In CV measurements, two well-defined anodic peaks were observed at +0.20 and +0.51 V (vs. a Ag/AgCl quasi-reference). The anodic peak at +0.20 V was attributed to the oxidation of HCOOH to CO2 on surface unblocked by CO, whereas the peak at +0.51 V was ascribed to the oxidation of surface-adsorbed CO (an intermediate product of HCOOH oxidation) and further oxidation of bulk HCOOH. From the onset potential and current density of the electro-oxidation of HCOOH, FePt nanoparticles exhibit excellent electrocatalytic activities as compared to Pt and other metal alloys. EIS measurements were carried out to further examine the reaction kinetics involved in the HCOOH electro-oxidation. The EIS responses were found to be strongly dependent on electrode potentials. At potentials more positive than −0.25 V (vs. Ag/AgCl), pseudo-inductive behavior was typically observed. At potentials between +0.3 and +0.5 V, the impedance response was found to reverse from the first quadrant to the second quadrant; such negative Faradaic impedance was indicative of the presence of an inductive component due to the oxidation of surface-adsorbed CO. The impedance responses returned to normal behavior at more positive potentials (+0.6 to +0.9 V). The mechanistic variation was attributed to the formation of different intermediates (CO or oxygen containing species) on the electrode surface in different potential regions. Two equivalent circuits were proposed to model these impedance behaviors.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
自己引用率: 10.3%
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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