Supported cluster catalysts synthesized to be small, simple, selective, and stable

被引:7
作者
Guan, Erjia [1 ,2 ]
Fang, Chia-Yu [1 ,2 ]
Yang, Dong [1 ]
Wang, Liang [3 ]
Xiao, Feng-Shou [3 ]
Gates, Bruce C. [1 ]
机构
[1] Univ Calif Davis, Dept Chem Engn, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Mat Sci & Engn, Davis, CA 95616 USA
[3] Zhejiang Univ, Dept Chem, Key Lab Appl Chem Zhejiang Prov, Hangzhou 310028, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
X-RAY-ABSORPTION; FINE-STRUCTURE SPECTROSCOPIES; METAL-ORGANIC FRAMEWORKS; RHODIUM PAIR-SITES; ELECTRON-MICROSCOPY; ORGANOMETALLIC CHEMISTRY; HETEROGENEOUS CATALYSTS; ETHYLENE HYDROGENATION; ETHENE HYDROGENATION; DINUCLEAR COMPLEXES;
D O I
10.1039/c8fd00076j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Molecular metal complexes on supports have drawn wide attention as catalysts offering new properties and opportunities for precise synthesis to make uniform catalytic species that can be understood in depth. Here we highlight advances in research with catalysts that are a step more complex than those incorporating single, isolated metal atoms on supports. These more complex catalysts consist of supported noble metal clusters and supported metal oxide clusters, and our emphasis is placed on some of the simplest and best-defined of these catalysts, made by precise synthesis, usually with organometallic precursors. Characterization of these catalysts by spectroscopic, microscopic, and theoretical methods is leading to rapid progress in fundamental understanding of catalyst structure and function, and to expansion of this class of materials. The simplest supported metal clusters incorporate two metal atoms eachthey are pair-site catalysts. These and clusters containing several metal atoms have reactivities determined by the metal nuclearity, the ligands on the metal, and the supports, which themselves are ligands. Metal oxide clusters are also included in the discussion presented here, with Zr6O8 clusters that are nodes in metal-organic frameworks being among those that are understood the best. The surface and catalytic chemistries of these metal oxide clusters are distinct from those of bulk zirconia. A challenge in using any supported cluster catalysts is associated with their possible sintering, and recent research shows how metal nanoparticles can be encapsulated in sheaths with well-defined porous structureszeolitesthat make them highly resistant to sintering.
引用
收藏
页码:9 / 33
页数:25
相关论文
共 51 条
[11]   COMPARTMENTAL LIGANDS - ROUTES TO HOMO-DINUCLEAR AND HETERO-DINUCLEAR COMPLEXES [J].
CASELLATO, U ;
VIGATO, PA .
CHEMICAL SOCIETY REVIEWS, 1979, 8 (02) :199-220
[12]   BISDIPHENYLPHOSPHINOMETHANE IN DINUCLEAR COMPLEXES [J].
CHAUDRET, B ;
DELAVAUX, B ;
POILBLANC, R .
COORDINATION CHEMISTRY REVIEWS, 1988, 86 :191-243
[13]   CRYSTAL AND MOLECULAR STRUCTURES OF DICHROMIUM TETRA-ACETATE DIHYDRATE AND DIRHODIUM TETRA-ACETATE DIHYDRATE [J].
COTTON, FA ;
DEBOER, BG ;
LAPRADE, MD ;
PIPAL, JR ;
UCKO, DA .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL CRYSTALLOGRAPHY AND CRYSTAL CHEMISTRY, 1971, B 27 (AUG15) :1664-&
[14]   Crystalline metal-organic frameworks (MOFs): synthesis, structure and function [J].
Dey, Chandan ;
Kundu, Tanay ;
Biswal, Bishnu P. ;
Mallick, Arijit ;
Banerjee, Rahul .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2014, 70 :3-10
[15]   Structural redetermination of Rh4(CO)12 at 293 and 173 K and analysis of the thermal motion in relation to the dynamical behavior [J].
Farrugia, LJ .
JOURNAL OF CLUSTER SCIENCE, 2000, 11 (01) :39-53
[16]  
Fortea-Pérez FR, 2017, NAT MATER, V16, P760, DOI [10.1038/nmat4910, 10.1038/NMAT4910]
[17]   Atomically dispersed supported metal catalysts: perspectives and suggestions for future research [J].
Gates, Bruce C. ;
Flytzani-Stephanopoulos, Maria ;
Dixon, David A. ;
Katz, Alexander .
CATALYSIS SCIENCE & TECHNOLOGY, 2017, 7 (19) :4259-4275
[18]   Synthesis and structure of tetrairidium clusters on TiO2 powder:: Characterization by infrared and extended X-ray absorption fine structure spectroscopies [J].
Goellner, JF ;
Guzman, J ;
Gates, BC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (06) :1229-1238
[19]   Stable Rhodium Pair Sites on MgO: Influence of Ligands and Rhodium Nuclearity on Catalysis of Ethylene Hydrogenation and H-D Exchange in the Reaction of H2 with D2 [J].
Guan, Erjia ;
Gates, Bruce C. .
ACS CATALYSIS, 2018, 8 (01) :482-487
[20]   Presence versus Proximity: The Role of Pendant Amines in the Catalytic Hydrolysis of a Nerve Agent Simulant [J].
Islamoglu, Timur ;
Ortuno, Manuel A. ;
Proussaloglou, Emmanuel ;
Howarth, Ashlee J. ;
Vermeulen, Nicolaas A. ;
Atilgan, Ahmet ;
Asiri, Abdullah M. ;
Cramer, Christopher J. ;
Farha, Omar K. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (07) :1949-1953