Nanoscale-Phase-Separated Pd-Rh Boxes Synthesized via Metal Migration: An Archetype for Studying Lattice Strain and Composition Effects in Electrocatalysis

被引:109
作者
Sneed, Brian T. [1 ]
Brodsky, Casey N. [1 ]
Kuo, Chun-Hong [1 ]
Lamontagne, Leo K. [1 ]
Jiang, Ying [2 ,3 ]
Wang, Yong [2 ,3 ]
Tao, Franklin [4 ]
Huang, Weixin [4 ]
Tsung, Chia-Kuang [1 ]
机构
[1] Boston Coll, Merkert Chem Ctr, Dept Chem, Chestnut Hill, MA 02467 USA
[2] Zhejiang Univ, Ctr Elect Microscopy, Hangzhou 310027, Zhejiang, Peoples R China
[3] Zhejiang Univ, Dept Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
[4] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
关键词
CORE-SHELL NANOPARTICLES; OXYGEN REDUCTION REACTION; BIMETALLIC NANOPARTICLES; ETHANOL OXIDATION; FORMIC-ACID; PREFERENTIAL OXIDATION; RHODIUM NANOPARTICLES; SYNERGISTIC CATALYSIS; POLYOL SYNTHESIS; CARBON-MONOXIDE;
D O I
10.1021/ja405387q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing syntheses of more sophisticated nanostructures comprising late transition metals broadens the tools to rationally design suitable heterogeneous catalysts for chemical transformations. Herein, we report a synthesis of Pd-Rh nanoboxes by controlling the migration of metals in a core shell nanoparticle. The Pd-Rh nanobox structure is a grid-like arrangement of two distinct metal phases, and the surfaces of these boxes are {100} dominant Pd and Rh. The catalytic behaviors of the particles were examined in electrochemistry to investigate strain effects arising from this structure. It was found that the trends in activity of model fuel cell reactions cannot be explained solely by the surface composition. The lattice strain emerging from the nanoscale separation of metal phases at the surface also plays an important role.
引用
收藏
页码:14691 / 14700
页数:10
相关论文
共 69 条
[1]   OPTICAL AND ELECTROCHEMICAL STUDY OF ELECTROCATALYSIS BY FOREIGN METAL ADATOMS - OXIDATION OF FORMIC-ACID ON RHODIUM [J].
ADZIC, RR ;
TRIPKOVIC, AV .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1979, 99 (01) :43-53
[2]   Ru-Pt core-shell nanoparticles for preferential oxidation of carbon monoxide in hydrogen [J].
Alayoglu, Selim ;
Nilekar, Anand U. ;
Mavrikakis, Manos ;
Eichhorn, Bryan .
NATURE MATERIALS, 2008, 7 (04) :333-338
[3]   Significant Enhancement of Formic Acid Oxidation Using Rhodium Nanostructures [J].
Balan, Beena K. ;
Sathe, Bhaskar R. .
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2012, 12 (12) :8994-8998
[4]   Converting nanocrystalline metals into alloys and intermetallic compounds for applications in catalysis [J].
Bauer, J. Chris ;
Chen, Xiaole ;
Liu, Qingsheng ;
Phan, Ting-Hao ;
Schaak, Raymond E. .
JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (03) :275-282
[5]   A review of methods of separation of the platinum-group metals through their chloro-complexes [J].
Bernardis, FL ;
Grant, RA ;
Sherrington, DC .
REACTIVE & FUNCTIONAL POLYMERS, 2005, 65 (03) :205-217
[6]   Strain-release mechanisms in bimetallic core-shell nanoparticles as revealed by Cs-corrected STEM [J].
Bhattarai, Nabraj ;
Casillas, Gilberto ;
Ponce, Arturo ;
Jose-Yacaman, Miguel .
SURFACE SCIENCE, 2013, 609 :161-166
[7]   Iodide ions control galvanic replacement growth of uniform rhodium nanotubes at room temperature [J].
Bi, Yingpu ;
Lu, Gongxuan .
CHEMICAL COMMUNICATIONS, 2008, (47) :6402-6404
[8]   The Solvent Matters: Kinetic versus Thermodynamic Shape Control in the Polyol Synthesis of Rhodium Nanoparticles [J].
Biacchi, Adam J. ;
Schaak, Raymond E. .
ACS NANO, 2011, 5 (10) :8089-8099
[9]   Emerging Strategies for the Total Synthesis of Inorganic Nanostructures [J].
Buck, Matthew R. ;
Schaak, Raymond E. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (24) :6154-6178
[10]   Oxygen reduction reaction on ruthenium and rhodium nanoparticles modified with selenium and sulfur [J].
Cao, DX ;
Wieckowski, A ;
Inukai, J ;
Alonso-Vante, N .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2006, 153 (05) :A869-A874