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

被引:3
|
作者
Neto, Edmundo S. Valerio [1 ,2 ]
Almeida, Caio V. S. [3 ]
Huang, Haoliang [4 ,5 ]
Russell, Andrea E. E. [4 ]
Eguiluz, Katlin I. B. [1 ,2 ]
Salazar-Banda, Giancarlo R. R. [1 ,2 ]
机构
[1] Inst Technol & Res ITP, Lab Electrochem & Nanotechnol LEN, BR-49032490 Aracaju, SE, Brazil
[2] Univ Tiradentes, Proc Engn Grad Programme PEP, BR-49032490 Aracaju, SE, Brazil
[3] Univ Fed Sao Carlos, Dept Chem, BR-13565905 Sao Carlos, SP, Brazil
[4] Univ Southampton, Sch Chem, Southampton SO17 1BJ, England
[5] Chinese Acad Sci, Shanghai Inst Appl Phys, Key Lab Interfacial Phys & Technol, Shanghai 201800, Peoples R China
关键词
binary catalysts; electroactivity; ethanol; nanowires; oxidation; C-C BOND; ELECTROCHEMICAL OXIDATION; TIN OXIDE; CARBON; PLATINUM; CATALYSTS; RHODIUM; NANOPARTICLES; METHANOL; ELECTROCATALYSTS;
D O I
10.1002/cctc.202300048
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The 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.
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页数:9
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