Electrochemical dissolution of gold in acidic medium

被引:87
作者
Cherevko, Serhiy [1 ]
Topalov, Angel A. [1 ]
Katsounaros, Ioannis [1 ]
Mayrhofer, Karl J. J. [1 ]
机构
[1] Max Planck Inst Eisenforsch GmbH, Dept Interface Chem & Surface Engn, D-40237 Dusseldorf, Germany
关键词
Noble metal corrosion; Gold dissolution; ICP-MS; Gold-platinum electrocatalysts; SULFURIC-ACID; PLATINUM; AU; ELECTROCATALYSTS; ELECTRODES; OXIDATION; RHODIUM; CELL;
D O I
10.1016/j.elecom.2012.11.040
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Polycrystalline gold dissolves at high potentials in acidic medium even without the presence of complexing agents. In the present work the dissolution of gold is quantitatively studied by an inductively coupled plasma mass spectrometer (ICP-MS) directly connected to an electrochemical scanning flow cell (SFC). It is shown that the onset of gold dissolution coincides with the onset of the formation of 2D surface oxide (ca. + 1.3 V-RHE). An increase in the upper potential limit (UPL) during potential cycling or an increase in the holding potential during potential steps leads to an enhancement in the amount of dissolved gold. Moreover, a change in the dominating mechanism for gold dissolution with increasing potential is found in transient experiments. At lower potentials, gold is dissolved mostly during the gold oxide reduction, while at higher potentials anodic dissolution is the dominating process. Finally, the possible application of gold for stabilization of PtAu-based fuel cell catalysts is discussed. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:44 / 46
页数:3
相关论文
共 27 条
[1]   ELEMENTARY STEPS OF ELECTROCHEMICAL OXIDATION OF SINGLE-CRYSTAL PLANES OF AU .2. A CHEMICAL AND STRUCTURAL BASIS OF OXIDATION OF THE (111) PLANE [J].
ANGERSTEINKOZLOWSKA, H ;
CONWAY, BE ;
HAMELIN, A ;
STOICOVICIU, L .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 228 (1-2) :429-453
[2]   RING-DISK ELECTRODE STUDY OF ANODIC BEHAVIOR OF GOLD IN 0.2M SULFURIC-ACID [J].
CADLE, SH ;
BRUCKENS.S .
ANALYTICAL CHEMISTRY, 1974, 46 (01) :16-20
[3]   Utilization of surface active sites on gold in preparation of highly reactive interfaces for alcohols electrooxidation in alkaline media [J].
Cherevko, Serhiy ;
Kulyk, Nadiia ;
Chung, Chan-Hwa .
ELECTROCHIMICA ACTA, 2012, 69 :190-196
[4]   Pt and Pd decorated Au nanowires: Extremely high activity of ethanol oxidation in alkaline media [J].
Cherevko, Serhiy ;
Xing, Xiaoli ;
Chung, Chan-Hwa .
ELECTROCHIMICA ACTA, 2011, 56 (16) :5771-5775
[5]   Nanoporous Pt@AuxCu100-x by Hydrogen Evolution Assisted Electrodeposition of AuxCu100-x and Galvanic Replacement of Cu with Pt: Electrocatalytic Properties [J].
Chereyko, Serhiy ;
Kulyk, Nadiia ;
Chung, Chan-Hwa .
LANGMUIR, 2012, 28 (06) :3306-3315
[6]   Degradation of Bimetallic Model Electrocatalysts: An In Situ X-Ray Absorption Spectroscopy Study [J].
Friebel, Daniel ;
Miller, Daniel J. ;
Nordlund, Dennis ;
Ogasawara, Hirohito ;
Nilsson, Anders .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (43) :10190-10192
[7]   Structural effects on trends in the deposition and dissolution of metal-supported metal adstructures [J].
Greeley, Jeffrey .
ELECTROCHIMICA ACTA, 2010, 55 (20) :5545-5550
[8]   WHY GOLD IS THE NOBLEST OF ALL THE METALS [J].
HAMMER, B ;
NORSKOV, JK .
NATURE, 1995, 376 (6537) :238-240
[9]   AuPt core-shell nanocatalysts with bulk Pt activity [J].
Hartl, Katrin ;
Mayrhofer, Karl J. J. ;
Lopez, Marco ;
Goia, Dan ;
Arenz, Matthias .
ELECTROCHEMISTRY COMMUNICATIONS, 2010, 12 (11) :1487-1489
[10]   NOVEL GOLD CATALYSTS FOR THE OXIDATION OF CARBON-MONOXIDE AT A TEMPERATURE FAR BELOW 0-DEGREES-C [J].
HARUTA, M ;
KOBAYASHI, T ;
SANO, H ;
YAMADA, N .
CHEMISTRY LETTERS, 1987, (02) :405-408