4.7 Article

Enhanced redox catalysis of electrochemical alcohol oxidation in alkaline medium by using Pt-Cu/C catalyst

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 926, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2022.166994

Keywords

Pt-Cu; Electrochemical catalysis; Alcohol oxidation; Bimetallic nanoparticle; H2O 2

Funding

  1. Xiamen University
  2. Changji University Department of Chemistry and Applied Chemistry
  3. China Scholarship Council (CSC) [201806370221]
  4. National Research Foundation of Korea [NRF-2019R1A2C2090249]

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In electrochemical alcohol oxidation reactions, alloying Pt with Cu significantly enhances the catalyst's activity and stability. Oxidative pretreatment of the carbon support introduces O-containing functional groups, stabilizing Cu δ+ species in bimetallic nanoparticles and improving catalysis. This work highlights the importance of support modification in enhancing the activity of electrocatalytic oxidation reactions in bimetallic nanoparticles.
In electrochemical alcohol oxidation reactions catalysed by supported Pt-based nanoparticles, the catalytic performance is highly correlated with the electron density accumulated over the metal's surface. The highly electronegative nature of Pt, affects the catalytic performance by accumulating electrons generated over the oxidative reaction on the Pt surface. It was found that alloying Cu to Pt enhances greatly the catalyst's activity and robustness. This enhancement is due to the redox reaction of Cu delta+ species into Cu-0 with the electrons generated during the reaction. Here, we show that an oxidative pretreatment of the carbon support XC-72R with HNO3 or H2O2 can further boost the catalysis of alcohol oxidation. This is mainly explained by the effect of enriched O-containing functional groups introduced in the support materials, which stabilize the presence of Cu delta+ species in the bimetallic Pt-Cu nanoparticles. This process increases the hydrophilic wettability, which enables more adsorption of reactant molecules and hydroxide ions over the catalyst's surface, as demonstrated by DFT calculations. The proposed catalytic system is applicable to a variety of substrates, including methanol, ethanol, isopropanol and sorbitol. Our work emphasizes the importance of support's modification in tuning the interaction within the bimetallic nanoparticles and thus enhancing the electrocatalytic oxidation reactions' activity. (C) 2022 Elsevier B.V. All rights reserved.

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