Carbon-graphene hybrid supporting platinum-tin electrocatalyst to enhance ethanol oxidation reaction

被引:10
作者
Bastos, Tarso L. [1 ]
Gelamo, Rogerio V. [2 ]
Colmati, Flavio [1 ]
机构
[1] Univ Fed Goias, Inst Quim, Ave Esperanca sn,Campus Samambaia, BR-74690900 Goiania, Go, Brazil
[2] Univ Fed Triangulo Mineiro, Inst Ciencias Tecnol & Exatas, Ave Doutor Randolfo Borges Jr 1250, BR-38064200 Uberaba, MG, Brazil
关键词
Direct ethanol fuel cell; Pt-Sn electrocatalyst; Ethanol oxidation reaction; Hybrid support; Graphene; OXYGEN REDUCTION REACTION; FUEL-CELL; ALLOY NANOPARTICLES; HIGH-PERFORMANCE; BLACK HYBRIDS; METHANOL; CATALYSTS; NANOCATALYSTS; ELECTROOXIDATION; NANOPLATELETS;
D O I
10.1007/s10800-023-02027-2
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Direct ethanol fuel cell (DEFC) is promising source for mobile and portable applications, but the electrocatalysts are based on metal noble alloys or doping elements to minimize the incomplete ethanol oxidation and poisoning effect. While the main problem persists, this study describes the enhancement of ethanol oxidation reaction by adding graphene (G) to Vulcan XC-72R carbon black (C) metal support, with different C/G ratios. The Graphene was prepared from exfoliated graphite following by dried at ambient temperature. The 60 wt% graphene hybrid support enhances the current density at 5% cyclic voltammetry (CV) and 127% chronoamperometry (CA) higher than carbon pure support in acid electrolyte, whereas in alkaline, graphene (60 wt%) showed the highest electrochemical activity with an increase of current 82% (CV) and 130% (CA). Therefore, we demonstrated the enhancement of the catalyst electrochemical activity in both electrolytes through a simple synthesis method. The 40 wt% carbon and 60 wt% graphene hybrid support achieving higher performance in ethanol oxidation, evidencing a potential application in DEFC.
引用
收藏
页码:1225 / 1237
页数:13
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