Template‐ and Surfactant‐Free Room Temperature Synthesis of Pt/C and Pt−Rh/C Nanowires/Nanoparticles for Ethanol Electro‐Oxidation

Author:

Neto Edmundo S. Valério12,Almeida Caio V. S.3ORCID,Huang Haoliang45,Russell Andrea E.4,Eguiluz Katlin I. B.12ORCID,Salazar‐Banda Giancarlo R.12ORCID

Affiliation:

1. Laboratory of Electrochemistry and Nanotechnology – LEN Institute of Technology and Research – ITP Aracaju Sergipe 49.032-490 Brazil

2. Processes Engineering Graduate Programme – PEP Tiradentes University Aracaju Sergipe 49.032-490 Brazil

3. Department of Chemistry Federal University of São Carlos São Carlos São Paulo 13.565-905 Brazil

4. School of Chemistry University of Southampton Southampton SO17 1BJ United Kingdom

5. Key Laboratory of Interfacial Physics and Technology Shanghai Institute of Applied Physics Chinese Academy of Sciences Shanghai 201800 China

Abstract

AbstractThe synthesis of Pt−Rh alloy nanowires (NWs) using straightforward methodologies remains a challenge. Here, carbon‐supported Pt and Pt−Rh nanowire catalysts were synthesised by chemical reduction at room temperature, without using surfactants or templates. The method of synthesis used yielded Pt/C NWs and a mixture of nanowires with some nanoparticles for the Pt−Rh/C catalysts (characterised using XRD, TEM, EDX, XPS, and XAS). The nanoparticles form due to differences in the surface energy and atomic radius between Pt and Rh. The binary NWs are found to be more active towards ethanol oxidation than the commercial Pt/C reference catalyst. Additionally, the Pt−Rh/C NW catalyst displays a specific activity 2.5‐fold higher than the Pt/C NWs and Pt/C reference catalysts after 15 min of chronoamperometric tests (at 0.5 V vs RHE). Thus, the synthesised carbon‐supported Pt NWs and Pt−Rh nanowires‐nanoparticles are promising alternatives for direct ethanol fuel cell anodes.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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