4.8 Article

Morphology-controlled synthesis of ternary Pt-Pd-Cu alloy nanoparticles for efficient electrocatalytic oxygen reduction reactions

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 174, Issue -, Pages 526-532

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcatb.2015.03.019

Keywords

Oxygen reduction reaction; Electrocatalysis; Ternary alloy nanoparticles; Morphology control; Galvanic displacement reaction

Funding

  1. Global Frontier R&D Program on Center for Multiscale Energy System [NRF-2012-M3A6A7054283]
  2. NRF - MSIP [2014-R1A2A2A04003865]
  3. KIST Institutional Program of Korea Institute of Science and Technology (KIST)
  4. New and Renewable Energy Core Technology Program of KETEP - MOTIE [2013-3030011320]
  5. Basic Science Research Program [NRF-2012R1A6A3A04040490]
  6. National Research Foundation of Korea [2011-0031571] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In the present work, we have accomplished morphology-controlled synthesis of ternary Pt-Pd-Cu alloy nanoparticles, particularly for efficient electrocatalytic oxygen reduction reactions. By controlling over the degree of galvanic displacement at room temperature, we selectively introduced porous and hollow architectures into Pt-decorated Pd-Cu alloy nanoparticles. Porous morphology was accompanied with partially facilitated Pt substitution reaction while hollow shape was exclusively achieved when the galvanic reaction was coupled with additional pre-treatment process which could eventually make the following displacement reaction more facile. Not only the both porous and hollow Pt@PdCu/C catalysts exhibited enhanced ORR performances compared to commercial Pt/C, but also they displayed outstanding durability. In addition, we investigated the alloying effects between Pt and Pd-Cu composite and the presumable influences of lattice strain through preliminary theoretical calculation to account for the enhanced ORR efficiency and durability of the present catalysts. (C) 2015 Elsevier B.V. All rights reserved.

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