TY - JOUR
T1 - Facile synthesis of aupd nanochain networks on carbon supports and their application as electrocatalysts for oxygen reduction reaction
AU - Cha, Areum
AU - Shim, Jun Ho
AU - Jo, Ara
AU - Lee, Sang Cheol
AU - Lee, Youngmi
AU - Lee, Chongmok
PY - 2014/4
Y1 - 2014/4
N2 - The present work reports the facile synthesis and characterization of carbon-supported porous Pd shell coated Au nanochain networks (AuPdNNs/C). By using Co nanoframes as sacrificial templates, AuPdNNs/C series have been prepared by a two-step galvanic replacement reaction (GRR) technique. In the first step, the Au metal precursor, HAuCl4, reacts spontaneously with the formed Co nanoframes through the GRR, resulting in Au nanochain networks (AuNNs). The second GRR is performed with various concentrations of Pd precursor (0.1, 1, and 10mM PdCl2), resulting in AuPdNNs/C. The synthesized AuPdNNs/C series are investigated as electrocatalysts for oxygen reduction reaction (ORR) in alkaline solution. The physical properties of the AuPdNNs/C catalysts are characterized by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), UV-vis absorption spectroscopy, and cyclic voltammetry (CV). Rotating disk electrode (RDE) voltammetric studies show that the Au0.8Pd0.2NNs/C (prepared using 1mM PdCl2) has the highest ORR activity among all the AuPdNNs/C series, which is comparable to commercial Pt catalyst (E-TEK). The ORR activity of AuPdNNs/C is presumably due to the enhanced Pd surface area and high porosity of Pd nanoshells.
AB - The present work reports the facile synthesis and characterization of carbon-supported porous Pd shell coated Au nanochain networks (AuPdNNs/C). By using Co nanoframes as sacrificial templates, AuPdNNs/C series have been prepared by a two-step galvanic replacement reaction (GRR) technique. In the first step, the Au metal precursor, HAuCl4, reacts spontaneously with the formed Co nanoframes through the GRR, resulting in Au nanochain networks (AuNNs). The second GRR is performed with various concentrations of Pd precursor (0.1, 1, and 10mM PdCl2), resulting in AuPdNNs/C. The synthesized AuPdNNs/C series are investigated as electrocatalysts for oxygen reduction reaction (ORR) in alkaline solution. The physical properties of the AuPdNNs/C catalysts are characterized by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), UV-vis absorption spectroscopy, and cyclic voltammetry (CV). Rotating disk electrode (RDE) voltammetric studies show that the Au0.8Pd0.2NNs/C (prepared using 1mM PdCl2) has the highest ORR activity among all the AuPdNNs/C series, which is comparable to commercial Pt catalyst (E-TEK). The ORR activity of AuPdNNs/C is presumably due to the enhanced Pd surface area and high porosity of Pd nanoshells.
KW - Electrocatalysis
KW - Galvanic replacement
KW - Gold-palladium nanostructure
KW - Non-platinum fuel cell electrode
KW - Oxygen reduction reaction
UR - http://www.scopus.com/inward/record.url?scp=84897451432&partnerID=8YFLogxK
U2 - 10.1002/elan.201300553
DO - 10.1002/elan.201300553
M3 - Article
AN - SCOPUS:84897451432
SN - 1040-0397
VL - 26
SP - 723
EP - 731
JO - Electroanalysis
JF - Electroanalysis
IS - 4
ER -