Probing the surfaces of heterogeneous catalysts by in situ IR spectroscopy

被引:423
作者
Lamberti, Carlo [3 ,4 ]
Zecchina, Adriano [3 ,4 ]
Groppo, Elena [1 ,2 ]
Bordiga, Silvia [1 ,2 ]
机构
[1] Univ Turin, NIS Ctr Excellence, Dept Inorgan Phys & Mat Chem, I-10135 Turin, Italy
[2] Univ Turin, INSTM Reference Ctr, I-10135 Turin, Italy
[3] Univ Turin, NIS Ctr Excellence, Dept Inorgan Phys & Mat Chem, I-10125 Turin, Italy
[4] Univ Turin, INSTM Reference Ctr, I-10125 Turin, Italy
关键词
SUPPORTED COPPER CHLORIDE; ION-EXCHANGED ZSM-5; METAL-ORGANIC FRAMEWORKS; SUM-FREQUENCY GENERATION; AB-INITIO CALCULATIONS; MICROPOROUS TITANOSILICATE ETS-10; OXIDATION CHANGES UNDERGONE; CATALYTICALLY ACTIVE GOLD; CR/SIO2 PHILLIPS CATALYST; NITRIC-OXIDE ADSORPTION;
D O I
10.1039/c0cs00117a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This critical review describes the reactivity of heterogeneous catalysts from the point of view of four simple, but essential for Chemistry, molecules (namely dihydrogen, carbon monoxide, nitrogen monoxide and ethylene) that are considered as probes or as reactants in combination with "in situ'' controlled temperature and pressure Infrared spectroscopy. The fundamental properties of H-2, CO, NO and C2H4 are shortly described in order to justify their different behaviour in respect of isolated sites in different environments, extended surfaces, clusters, crystalline or amorphous materials. The description is given by considering some "key studies'' and trying to evidence similarities and differences among surfaces and probes (572 references).
引用
收藏
页码:4951 / 5001
页数:51
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