Carbon-Supported Pt Nanoparticles Modified with CuO for the Electrooxidation of Glycerol in Alkaline Electrolyte

被引:0
|
作者
Sieben, Juan Manuel [1 ,2 ]
Alvarez, Andrea A. [3 ]
Sanchez, Miguel D. [4 ]
机构
[1] Univ Nacl Sur, Dept Quim, B98000CPB, Bahia Blanca, Argentina
[2] Univ Nacl Sur, INQUISUR CONICET, B98000CPB, Bahia Blanca, Argentina
[3] Univ Nacl Sur, Inst Ingn Electroquim & Corros INIEC, B8000CPB, Bahia Blanca, Argentina
[4] Univ Nacl Sur UNS, Dept Fis, Inst Fis Sur IFISUR, CONICET, B8000CPB, Bahia Blanca, Argentina
来源
ACS APPLIED ENERGY MATERIALS | 2024年 / 7卷 / 15期
关键词
glycerol oxidation; CuO/C hybrid support; differentCuO content on carbon; Pt nanoparticles; pulsedmicrowave-assisted polyol method; ETHANOL ELECTROOXIDATION; FUEL-CELL; OXIDATION; METHANOL; PT/C; ELECTROCATALYSTS; CATALYSTS; PLATINUM; TEMPERATURE; PERFORMANCE;
D O I
10.1021/acsaem.4c01299
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
In this work, a series of Pt-CuO(x)/C materials with different metal oxide contents were evaluated as electrocatalysts for the glycerol oxidation reaction (GOR) in an alkaline medium. CuO nanoparticles of ca. 6 nm were prepared by a precipitation/calcination route and incorporated into the carbon support with a weight percentage from 0 to 30. Platinum nanoparticles of ca. 3 nm were deposited over the different hybrid CuO(x)/C materials via the ethylene glycol reduction under pulsed microwave heating conditions. The electrochemical experiments showed that the onset potential for the GOR on the bimetallic Pt-CuO(x)/C electrodes is shifted negatively by ca. 160 mV, and the charge transfer resistance is significantly reduced compared to Pt/C, indicating that CuO facilitates both the electron charge transfer kinetics and the oxidation of the adsorbed intermediates. The most active electrode material, Pt-CuO(30)/C (30 wt % CuO on carbon), developed 3.5 times higher activity than Pt/C. This bimetallic electrode retained more than 90% of its initial activity after an accelerated cycling test.
引用
收藏
页码:6677 / 6686
页数:10
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