Catalysts for oxygen reduction reaction based on nanocrystals of a Pt or Pt-Pd alloy shell supported on a Au core

被引:21
作者
Venarusso, L. B. [1 ]
Bettini, J. [2 ]
Maia, G. [1 ]
机构
[1] Univ Fed Mato Grosso do Sul, Inst Chem, Av Senador Filinto Muller 1555, BR-79074460 Campo Grande, MS, Brazil
[2] Brazilian Nanotechnol Natl Lab LNNano, Rua Giuseppe Maximo Scolfaro 10000, BR-13083100 Campinas, SP, Brazil
关键词
Electrochemistry; Oxygen reduction reaction; Nanocrystal; Nanodendrite; Platinum; Gold; ENHANCED RAMAN-SPECTROSCOPY; ELECTROCATALYTIC ACTIVITY; PALLADIUM ELECTRODE; AT-PD; NANOPARTICLES; GOLD; MONOLAYER; NANODENDRITES; STABILITY; OXIDATION;
D O I
10.1007/s10008-016-3181-z
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Nanocrystals (NCs) of a Pt or Pd or Pt-Pd alloy shell supported on a Au core were synthesized and dripped onto a glassy carbon (GC) surface to generate thin films. Their electrocatalytic activity towards the oxygen reduction reaction (ORR) was studied employing hydrodynamic cyclic voltammetry. Of the Pt or Pt-Pd alloy electrocatalysts synthesized over a Au core (including Au cores produced from redox-transmetalation of Ni cores), Pt-Pd@Au, Pt@Au, and Pt@Au' NCs-which contained heterogeneous NCs with spherical, triangular, squared, pentagonal, hexagonal, heptagonal, and rod-like shapes, with large (about 80 nm in several cases), well-defined crystalline structures, and evidenced a nanodendritic Pt or Pt-Pd alloy covering pattern at the NC surface-exhibited high electrocatalytic activity towards ORR and high stability (without dissolution of inner metallic nanoparticles such as Au) after 10,000 potential scans-features that suggest their utility for use in acid fuel cells.
引用
收藏
页码:1753 / 1764
页数:12
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