Effect of uniformity and surface morphology of Pt nanoparticles to enhance oxygen reduction reaction in polymer electrolyte membrane fuel cells

被引:15
|
作者
Lim, Su-yeong [1 ,2 ]
Kim, Sun-, I [1 ]
Lee, Min Seong [1 ,2 ]
Bak, Su-Jeong [1 ,2 ]
Lee, Duck Hyun [1 ]
Kwon, Se-Hun [2 ]
Kim, Taehyo [1 ]
机构
[1] Korea Inst Ind Technol, Green Mat & Processes R&D Grp, Ulsan, South Korea
[2] Pusan Natl Univ, Dept Mat Sci & Engn, Busan, South Korea
关键词
Fuel cell efficiency; Oxygen reduction; Polymer electrolyte; Surface morphology; CATALYST SUPPORT; HIGH-PERFORMANCE; PARTICLE-SIZE; PEMFC; CARBON; CATHODE; DURABILITY; GRAPHENE; DEGRADATION; ORR;
D O I
10.1016/j.ijhydene.2022.06.264
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
Platinum (Pt)-based electrocatalysts supported by reduced graphene oxide (rGO) is fabricated under microwave-assisted polyol method with various nucleation and growth conditions. The surface morphologies of the Pt nanoparticles (NPs) under various reaction conditions owing to different Pt NP sizes and inter-particle spacings are investigated by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, thermogravimetric analysis, cyclic and linear sweep voltammetry, and electrochemical impedance spectroscopy. The synthesized Pt/rGO catalyst under nucleation and growth times of 10 s and 50 s, respectively, exhibits excellent catalytic activity with increased electrochemical surface area, high density, good uniformity and surface morphology with a particle size and inter-particle spacing of 2.16 nm and 17.2 nm, respectively. These results elucidate the relationship between the Pt NP morphology distribution and oxygen reduction reaction of catalysts in polymer electrolyte membrane fuel cell systems. We also highlight the important role of size and inter-particle spacing on the Pt electrochemical catalystic performance. (c) 2022 The Author(s). Published by Elsevier Ltd on behalf of Hydrogen Energy Publications LLC. This is an open access article under the CC BY license (http://creativecommons.org/ licenses/by/4.0/).
引用
收藏
页码:29456 / 29466
页数:11
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