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Preparation of Pt/graphene catalysts for polymer electrolyte membrane fuel cells by strong electrostatic adsorption technique

石墨烯 零电荷点 吸附 循环伏安法 催化作用 铂金 电化学 无机化学 材料科学 化学工程 化学 分析化学(期刊) 电极 纳米技术 物理化学 有机化学 工程类
作者
Sukanya Pothaya,John R. Regalbuto,John R. Monnier,Konlayutt Punyawudho
出处
期刊:International Journal of Hydrogen Energy [Elsevier BV]
卷期号:44 (48): 26361-26372 被引量:25
标识
DOI:10.1016/j.ijhydene.2019.08.110
摘要

The Pt/graphene catalysts were prepared by using strong electrostatic adsorption (SEA) technique for polymer electrolyte membrane fuel cell (PEMFC). The pH shift was considered and the point of zero charge (PZC) of graphene was acquired at pH about 5.2. Due to the mid-to-low PZC, the cationic precursor (i.e., platinum tetra-ammine ([NH3)4 Pt]2+ or PTA) was chosen. After graphene surface was treated to be anionic substrate, the PTA was added and adsorbed onto the graphene by electrostatic force. Pt metals between before and after adsorption were determined by inductively coupled plasma spectroscopy (ICP) in order to consider Pt percent weight. After reduction in hydrogen environment, Pt/graphene catalysts were made. The second adsorption including the reduction was repeated in order to obtain the high Pt percentage such as 21.5%wt. The average particle sizes (ca. 2.2 nm) and distribution of Pt were inspected using transmission electron microscopy (TEM), where the crystalline structures were verified by X-Ray diffraction (XRD). Electrochemical properties were tested using cyclic voltammetry (CV) and the accelerated durability test (ADT) was also carried out. The oxygen reduction reaction (ORR) was also carried out, where the specific activity and mass activity were examined. It was observed from ADT that mass activity lost about 33%. Furthermore, the ORR was performed to verify the first order reaction, as well as to determine the mechanism path way for four electron transfer. Moreover, the kinetic constant of the ORR was also estimated.

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