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Pd@Pt Core-Shell Concave Decahedra: A Class of Catalysts for the Oxygen Reduction Reaction with Enhanced Activity and Durability

  • Xue Wang
  • , Madeline Vara
  • , Ming Luo
  • , Hongwen Huang
  • , Aleksey Ruditskiy
  • , Jinho Park
  • , Shixiong Bao
  • , Jingyue Liu
  • , Jane Howe
  • , Miaofang Chi
  • , Zhaoxiong Xie
  • , Younan Xia*
  • *Corresponding author for this work

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

Abstract

We report a facile synthesis of multiply twinned Pd@Pt core-shell concave decahedra by controlling the deposition of Pt on preformed Pd decahedral seeds. The Pt atoms are initially deposited on the vertices of a decahedral seed, followed by surface diffusion to other regions along the edges/ridges and then across the faces. Different from the coating of a Pd icosahedral seed, the Pt atoms prefer to stay at the vertices and edges/ridges of a decahedral seed even when the deposition is conducted at 200°C, naturally generating a core-shell structure covered by concave facets. The nonuniformity in the Pt coating can be attributed to the presence of twin boundaries at the vertices, as well as the {100} facets and twin defects along the edges/ridges of a decahedron, effectively trapping the Pt adatoms at these high-energy sites. As compared to a commercial Pt/C catalyst, the Pd@Pt concave decahedra show substantial enhancement in both catalytic activity and durability toward the oxygen reduction reaction (ORR). For the concave decahedra with 29.6% Pt by weight, their specific (1.66 mA/cm2Pt) and mass (1.60 A/mgPt) ORR activities are enhanced by 4.4 and 6.6 times relative to those of the Pt/C catalyst (0.36 mA/cm2Pt and 0.32 A/mgPt, respectively). After 10 000 cycles of accelerated durability test, the concave decahedra still exhibit a mass activity of 0.69 A/mgPt, more than twice that of the pristine Pt/C catalyst.
Original languageEnglish
Pages (from-to)15036-15042
JournalJournal of the American Chemical Society
Volume137
Issue number47
DOIs
Publication statusPublished - 13 Nov 2015
Externally publishedYes

Bibliographical note

Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].

Funding

This work was supported in part by start-up funds from the Georgia Institute of Technology and a grant from the NSF (CHE 1505441). As visiting Ph.D. students, X.W., M.L., H.H., and S.B. also received partial support from the China Scholarship Council. High-resolution imaging and tomography electron microscopy were performed through a user project supported by the ORNL’s Center for Nanophase Materials Sciences, which is a U.S. DOE Office of Science User Facility (M.C.). J.L. acknowledges the support by Arizona State University and the use of facilities in the John M. Cowley Center for High Resolution Electron Microscopy at Arizona State University.

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