Issue 34, 2015

Enhanced methanol electrooxidation at Pt skin@PdPt nanocrystals

Abstract

Pt skin growth over PdPt alloy nanocrystals has been described using a simple wet chemical method, where a layer-by-layer epitaxial deposition of Pt on PdPt could be understood by the Stranski–Krastanov mechanism. Initial PdPt alloy nanocrystals grown in a simple wet-chemical method, in the presence of a reducing solvent like N-methyl pyrrolidone (NMP) and a stabilizer like polyvinyl pyrrolidone (PVP), have been used as the substrate for secondary growth of a Pt thin layer. Surface changes have been observed during step-by-step growth of polyhedral Pt skin@PdPt nanocrystals originating from nearly octahedral geometries of PdPt. The methanol electrooxidation activities of two different Pt skin@PdPt nanostructures have been compared with PdPt nanocrystals with similar compositions but without skin structures and commercial RuPt catalysts. A gain factor of 8 towards electrooxidation of methanol in acidic media with activities of 1950 mA mgPt−1 and 3.1 mA cmPt−2 (with lower onset potential compared to the RuPt commercial catalyst), which is believed to be much higher compared to that of previous reports and state-of-art RuPt/C catalysts, indicating better surface properties and core-alloy formation along with improved intraparticle active interfacial sites. Additionally, exciting results of electrooxidation of ethanol and ethylene glycol with 70% and 58% activity retention respectively, after 5000 cycles are also found, demonstrating a facile C–C breaking in such C2 type alcohols.

Graphical abstract: Enhanced methanol electrooxidation at Pt skin@PdPt nanocrystals

Supplementary files

Article information

Article type
Paper
Submitted
22 May 2015
Accepted
27 Jul 2015
First published
28 Jul 2015

J. Mater. Chem. A, 2015,3, 17771-17779

Author version available

Enhanced methanol electrooxidation at Pt skin@PdPt nanocrystals

B. Kakade, I. Patil, M. Lokanathan and A. Swami, J. Mater. Chem. A, 2015, 3, 17771 DOI: 10.1039/C5TA03736K

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