Reactivity of Surface Species in Heterogeneous Catalysts Probed by In Situ X-ray Absorption Techniques

被引:547
作者
Bordiga, Silvia [1 ,2 ,3 ]
Groppo, Elena [1 ,2 ,3 ]
Agostini, Giovanni [1 ,2 ,3 ]
van Bokhoven, Jeroen A. [4 ,5 ]
Lamberti, Carlo [1 ,2 ,3 ]
机构
[1] Univ Turin, Dept Chem, I-10125 Turin, Italy
[2] Univ Turin, NIS Ctr Excellence, I-10125 Turin, Italy
[3] INSTM Reference Ctr, I-10125 Turin, Italy
[4] Swiss Fed Inst Technol, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[5] Paul Scherrer Inst Scherrer Inst, Swiss Light Source, Lab Catalysis & Sustainable Chem LSK, Villigen, Switzerland
关键词
METAL-ORGANIC-FRAMEWORK; FINE-STRUCTURE EXAFS; ENERGY-DISPERSIVE EXAFS; NEAR-EDGE STRUCTURE; DENSITY-FUNCTIONAL THEORY; MULTIPLE-SCATTERING APPROACH; SUPPORTED COPPER CHLORIDE; MAGNETIC CIRCULAR-DICHROISM; NEGATIVE THERMAL-EXPANSION; OVER-EXCHANGED FE/ZSM5;
D O I
10.1021/cr2000898
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Starting from the late seventies, the progressively increased availability of synchrotron light sources allowed the execution of experiments requiring a high X-ray flux in a continuous interval. In particular, XAFS techniques are extremely powerful to shed light on the structure and reactivity of surface species in heterogeneous catalysts, in many steps of the catalyst life and also during the catalytic act. A quantitative EXAFS and XANES analysis, possible only in these conditions, was fundamental to reveal the local structure of carbonyl species. IR spectroscopy gave independent information on the fraction of chromium sites active in ethylene polymerization on the Phillips catalysts as a function of polymerization conditions, in well agreement with the values obtained by XANES. The second is the experimental hutch, where the experiment is performed. The third is the control room, where where scientists monitor the experiment and perform a first data analysis.
引用
收藏
页码:1736 / 1850
页数:115
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