Journal
ACS CATALYSIS
Volume 5, Issue 9, Pages 5123-5134Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b01011
Keywords
platinum; ruthenium; electroless deposition; bimetallic catalyst; strong metal-metal interaction
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Funding
- University of South Carolina ASPIRE II Grant
- Div Of Chem, Bioeng, Env, & Transp Sys
- Directorate For Engineering [1160036] Funding Source: National Science Foundation
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Two series of Pt@Ru/C and Ru@Pt/C bimetallic catalysts have been prepared by an electroless deposition (ED) method. For Pt@Ru/C compositions, a new ED bath was developed using Ru(NH3)(6)Cl-3 as the Ru precursor and HCOOH as the reducing agent. For Ru@Pt/C preparations, a standard bath using H2PtCl6 and DMAB as the Pt precursor and reducing agent, respectively, was employed. The Pt@Ru/C and Ru@Pt/C bimetallic catalysts have been characterized by temperature-programmed reduction (TPR), selective chemisorption, X-ray photoelectron spectroscopy (XPS), and scanning transmission electron microscopy (STEM) with X-ray energy dispersive spectroscopy (XEDS). TPR and selective chemisorption (H-2 titration of oxygen-precovered surfaces) experiments have confirmed the existence of strong surface interactions between Pt and Ru, as evidenced by hydrogen spillover of Pt to Ru (Pt-assisted reduction of oxygen precovered Ru). XPS analyses also showed e(-) transfer from Pt to Ru on the bimetallic surface, again indicating strong surface interactions between Pt and Ru. Finally, the STEM images and XEDS elemental maps provided strong visual evidence of targeted deposition of the secondary metal on the primary metal. The elemental maps confirmed that individual nanoparticles of both Pt@Ru/C and Ru@Pt/C catalysts prepared by ED were bimetallic, with excellent association between the primary and the secondary metals.
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