磷酸修饰铂纳米粒子作为直接甲醇燃料电池耐甲醇氧还原电催化剂

IF 2.2 4区 工程技术 Q3 ELECTROCHEMISTRY
Jung-goo Choi, Kahyun Ham, Sungyool Bong, Jaeyoung Lee
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引用次数: 4

摘要

在直接甲醇燃料电池系统(DMFC)中,缺点之一是甲醇交叉。甲醇从阳极穿过膜进入阴极,在电池中产生混合电位。只有Pt基催化剂能够在DMFC的苛刻酸性条件下用作氧还原反应(ORR)的阴极。然而,由于Pt对甲醇氧化反应的高活性,它导致了混合电势。为了克服这种情况,通过控制反应物吸附或反应动力学,开发具有甲醇耐受性的Pt基催化剂是非常重要的。采用改进的多元醇法在DMFC中制备了磷酸修饰Pt/C阴极催化剂。磷酸根离子结合到Pt/C的碳上,围绕着游离的Pt表面,只阻止甲醇在Pt上的吸附,而不是氧气。与原始Pt/C相比,它可以抑制甲醇在氧气环境中的氧化,从而获得高DMFC性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phosphate-decorated Pt Nanoparticles as Methanol-tolerant Oxygen Reduction Electrocatalyst for Direct Methanol Fuel Cells
In a direct methanol fuel cell system (DMFC), one of the drawbacks is methanol crossover. Methanol from the anode passes through the membrane and enters the cathode, causing mixed potential in the cell. Only Pt-based catalysts are capable of operating as cathode for oxygen reduction reaction (ORR) in a harsh acidic condition of DMFC. However, it causes mixed potential due to high activity toward methanol oxidation reaction of Pt. To overcome this situation, developing Pt-based catalyst that has methanol tolerance is significant, by controlling reactant adsorption or reaction kinetics. Pt/C decorated with phosphate ion was prepared by modified polyol method as cathode catalyst in DMFC. Phosphate ions, bonded to the carbon of Pt/C, surround free Pt surface and block only methanol adsorption on Pt, not oxygen. It leads to the suppression of methanol oxidation in an oxygen atmosphere, resulting in high DMFC performance compared to pristine Pt/C.
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来源期刊
CiteScore
6.30
自引率
8.10%
发文量
44
期刊介绍: Covering fields: - Batteries and Energy Storage - Biological Electrochemistry - Corrosion Science and Technology - Electroanalytical Chemistry and Sensor Technology - Electrocatalysis - Electrochemical Capacitors & Supercapcitors - Electrochemical Engineering - Electrodeposition and Surface Treatment - Environmental Science and Technology - Fuel Cells - Material Electrochemistry - Molecular Electrochemistry and Organic Electrochemistry - Physical Electrochemistry - Solar Energy Conversion and Photoelectrochemistry
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