Understanding Pt Nanoparticle Anchoring on Graphene Supports through Surface Functionalization

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• 作者：Le Xin ; Fan Yang ; Somaye Rasouli ; Yang Qiu ; Zhe-Fei Li ; Aytekin Uzunoglu ; Cheng-Jun Sun ; Yuzi Liu ; Paulo Ferreira ; Wenzhen Li ; Yang Ren ; Lia A. Stanciu ; Jian Xie
• 刊名：ACS Catalysis
• 出版年：2016
• 出版时间：April 1, 2016
• 年：2016
• 卷：6
• 期：4
• 页码：2642-2653
• 全文大小：1091K
• ISSN：2155-5435

文摘

The enhancement of Pt nanoparticle anchoring strength and dispersion on carbon supports is highly desirable in polymer electrolyte membrane fuel cells (PEMFCs) as well as in other catalysis processes. Presented here is a comprehensive study of the interaction between catalyst nanoparticles and carbon supports in terms of the electronic structure change and its effects on the electrocatalytic performance of supported catalysts. Graphene was chosen as an ideal model support because the unique 2-D structure allows the direct investigation of the interaction with supported metal nanoparticles at their interface. We developed a facile strategy to covalently graft p-phenyl SO₃H—or p-phenyl NH₂—groups onto the graphene surface. The functional groups were found to not only facilitate the homogeneous distribution of Pt nanoparticles on the surface of graphene supports and reduce the Pt average particle size but also strengthen the interaction of the Pt atoms with the functional groups and, consequently, minimize the migration/coalescence of the Pt nanoparticles in the course of accelerated durability tests. The experimental results from both X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) demonstrate the electron density shift from Pt to graphene supports with the strength of the Pt–graphene interaction following the trend of Pt/p-phenyl NH₂-graphene > Pt/p-phenyl SO₃H-graphene > Pt/graphene. This study will shed light on strategies to improve not only the durability but also the activity of the metal nanoparticles via the functionalization of the catalyst supports in the catalysis field.