Surfactant-Concentration-Dependent Shape Evolution of AuPd Alloy Nanocrystals from Rhombic Dodecahedron to Trisoctahedron and Hexoctahedron

被引:86
作者
Zhang, Jiawei [1 ,2 ]
Hou, Changping [1 ,2 ]
Huang, Huang [1 ,2 ]
Zhang, Lei [1 ,2 ]
Jiang, Zhiyuan [1 ,2 ]
Chen, Guangxu [1 ,2 ]
Jia, Yanyan [1 ,2 ]
Kuang, Qin [1 ,2 ]
Xie, Zhaoxiong [1 ,2 ]
Zheng, Lansun [1 ,2 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Dept Chem, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
gold; palladium; alloys; nanostructures; surfactants; HIGH-INDEX FACETS; SINGLE-CRYSTAL ELECTRODES; METAL NANOCRYSTALS; ELECTROCATALYTIC ACTIVITIES; BIMETALLIC NANOCRYSTALS; PLATINUM NANOCRYSTALS; CATALYTIC-PROPERTIES; GOLD NANOPARTICLES; PD; PALLADIUM;
D O I
10.1002/smll.201202013
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The surface structure-controlled synthesis of noble metal nanocrystals (NCs) bounded by high-index facets has become a hot research topic due to their potential to significantly improve catalytic performance. This study reports the preparation of monodisperse AuPd alloy NCs with systematic shape evolution from rhombic dodecahedral (RD) to trisoctahedral (TOH), and hexoctahedral (HOH) structures by varying the concentration of surfactant in the surfactant-mediated synthesis. The as-prepared three kinds of alloy NCs possess almost the same size and composition as each other. It is suggested that the surfactant containing long-chain octadecyltrimethyl ammonium (OTA+) ions plays a key role in the formation of high index facets, and the crystal growth kinetics may also have an effect on the formation of different nanocrystal morphologies. In addition, the catalytic activities of these NCs are evaluated by structure-sensitive reactions, including ethanol electro-oxidation and the catalytic reduction of 4-nitrophenol (4-NPh). These three types of AuPd alloy NCs exhibit different catalytic selectivities towards these two reactions. The catalytic activities toward electro-oxidation of ethanol are in the order of HOH > RD > TOH, which follows the order of their corresponding surface energies. However, the activities toward catalytic reduction of 4-NPh are in the order of RD > TOH > HOH, which should be related to the local structure of the surfaces.
引用
收藏
页码:538 / 544
页数:7
相关论文
共 50 条
[1]  
[Anonymous], ANGEW CHEM INT ED
[2]  
[Anonymous], 2008, ANGEW CHEMIE, DOI DOI 10.1002/ANGE.200802750
[3]   The promotional effect of gold in catalysis by palladium-gold [J].
Chen, MS ;
Kumar, D ;
Yi, CW ;
Goodman, DW .
SCIENCE, 2005, 310 (5746) :291-293
[4]   VEGARD LAW [J].
DENTON, AR ;
ASHCROFT, NW .
PHYSICAL REVIEW A, 1991, 43 (06) :3161-3164
[5]   Seed-Mediated Co-reduction: A Versatile Route to Architecturally Controlled Bimetallic Nanostructures [J].
DeSantis, Christopher J. ;
Sue, Aaron C. ;
Bower, Matthew M. ;
Skrabalak, Sara E. .
ACS NANO, 2012, 6 (03) :2617-2628
[6]   Pd and Pt catalysts modified by alloying with Au in the selective oxidation of alcohols [J].
Dimitratos, Nikolaos ;
Villa, Alberto ;
Wang, Di ;
Porta, Francesca ;
Su, Dangsheng ;
Prati, Laura .
JOURNAL OF CATALYSIS, 2006, 244 (01) :113-121
[7]   Simple Reductant Concentration-Dependent Shape Control of Polyhedral Gold Nanoparticles and Their Plasmonic Properties [J].
Eguchi, Miharu ;
Mitsui, Daisuke ;
Wu, Hsin-Lun ;
Sato, Ryota ;
Teranishi, Toshiharu .
LANGMUIR, 2012, 28 (24) :9021-9026
[8]   Solvent-free oxidation of primary alcohols to aldehydes using Au-Pd/TiO2 catalysts [J].
Enache, DI ;
Edwards, JK ;
Landon, P ;
Solsona-Espriu, B ;
Carley, AF ;
Herzing, AA ;
Watanabe, M ;
Kiely, CJ ;
Knight, DW ;
Hutchings, GJ .
SCIENCE, 2006, 311 (5759) :362-365
[9]   Shaping binary metal nanocrystals through epitaxial seeded growth [J].
Habas, Susan E. ;
Lee, Hyunjoo ;
Radmilovic, Velimir ;
Somorjai, Gabor A. ;
Yang, Peidong .
NATURE MATERIALS, 2007, 6 (09) :692-697
[10]   Preparation and electrochemical characterization of palladium single crystal electrodes in 0.1 M H2SO4 and HClO4 part I.: Low-index phases [J].
Hara, M. ;
Linke, U. ;
Wandlowski, Th. .
ELECTROCHIMICA ACTA, 2007, 52 (18) :5733-5748