Facile solvothermal synthesis of Pt-Cu nanocatalyst with improved electrocatalytic activity toward methanol oxidation

被引:1
|
作者
Mehmood, Muhammad Harts [1 ]
Tariq, Muhammad [1 ]
Hassan, Ayaz [2 ]
Raziq, Abdul [1 ]
Rahim, Abdur [3 ]
Khan, Jehangeer [1 ]
机构
[1] Univ Peshawar, Natl Ctr Excellence Phys Chem, Peshawar 25120, Pakistan
[2] Univ Sao Paulo, Inst Quim Sao Carlos, Sao Carlos, SP, Brazil
[3] COMSATS Univ Islamabad, IRCBM, Lahore Campus, Lahore, Pakistan
关键词
cyclic voltammetry; electrochemical activity; chronoamperometry; fuel cells; DMFC; REAL SURFACE-AREA; PLATINUM; NANOPARTICLES; ELECTRODES; NANOWIRES;
D O I
10.2298/JSC190131041M
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A binary metal nanocatalyst of platinum and copper was synthesized using a facile solvothermal process (polyol method). The synthesized catalyst was characterized using energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical performance of the synthesized carbon supported binary metal catalyst, Pt-Cu/C, toward methanol oxidation reaction was checked and then compared with the commercial Pt/C (ETEK) catalyst, using cyclic voltammetry and chronoamperometric techniques. The Pt-Cu/C catalyst was found to be cubic in shape with indentations on the particle surface, having platinum to copper atomic composition of 4:1, i.e., (Pt4Cu). The peak current density for Pt-Cu/C catalyst recorded as 2.3 mA cm(2) at 0.7 V (vs Ag/AgCl) and 50 mV s(-1), was two times higher than the current density of the commercially available Pt/C catalyst (1.16 mA cm(2) at 0.76 V). Moreover, the Pt-Cu/C catalyst was found to be more durable than the commercial Pt/C catalyst, as the Pt-Cu/C retained 89 % of its initial current density, while the commercial Pt/C catalyst retained 65 % of its initial current density after 300 potential cycles.
引用
收藏
页码:1155 / 1167
页数:13
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