Effect of particle size on the activity and durability of the Pt/C electrocatalyst for proton exchange membrane fuel cells

• Published in: Applied catalysis. B, Environmental Environmental, 2012-01, Vol.111-112, p.264-270
• Main Authors: Xu, Zhuang, Zhang, Huamin, Zhong, Hexiang, Lu, Qiuhong, Wang, Yunfeng, Su, Dangsheng
• Format: Article
• Language: English
• Subjects: Activity; Applied sciences; Catalysis; Chemistry; Durability; Electrochemistry; Energy; Energy. Thermal use of fuels; Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc; Exact sciences and technology; Fuel cells; General and physical chemistry; Kinetics and mechanism of reactions; Particle size; Proton exchange membrane fuel cells; Pt/C electrocatalyst; Surface physical chemistry; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
• ISSN: 0926-3373; 1873-3883
• DOI: 10.1016/j.apcatb.2011.10.007

[Display omitted] ► In situ electrochemical synthesis for Pt with various particle sizes. ► Surface specific activity and electrochemical stability improved with Pt particle size increase. ► Reduced defects on the Pt surface weaken the adsorption of oxygenated species releasing more available active sites. ► Fuel cell durability sharply increased when Pt exceeding 3nm. ► Designing Pt with more face atom occupation would obtain more active and durable PEMFC catalyst. Carbon supported Pt (Pt/C) with various average particle sizes ranging from sub 3nm to 6.5nm were in situ prepared and characterized at the cathode of proton exchange membrane fuel cells (PEMFCs). A clear Pt particle size effect on both the catalytic activity for oxygen reduction reaction (ORR) and the durability of the electrocatalyst was revealed. With the Pt particle size increase, both the surface specific activity and the electrochemical stability of Pt/C improved; however, the mass specific activity of Pt/C is balanced by the electrochemical surface area loss. The reduced occupation of corner and edge atoms on the Pt surface during the Pt particle size increase is believed to weaken the adsorption of the oxygenated species on Pt, and thereafter releases more available active sites for ORR and also renders the Pt surface a stronger resistance against potential cycling. It is therefore proposed that by designing the Pt microstructure with more face atoms on the surface, cathode electrocatalyst with both improved activity and enhanced durability would be developed for PEMFCs.