Role of surface science in catalysis

被引:82
作者
Sinfelt, JH [1 ]
机构
[1] ExxonMobil Res & Engn Co, Oldwick, NJ 08858 USA
关键词
catalysis; chemisorption; adsorption isotherms; adsorption kinetics; physical adsorption; surface chemical reaction; clusters; single crystal surfaces;
D O I
10.1016/S0039-6028(01)01532-1
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
Around the time of World War I, Langmuir advanced a simple theory of chemisorption and showed how it could be used to formulate rate laws for reactions occurring on surfaces. From that time on, surface science has played an important role in heterogeneous catalysis. Between the two world wars, simple studies of extents of adsorption by catalyst surfaces led to the concept of activated adsorption and to a universally used method for determining the high surface areas associated with the pore structures of catalytic materials. After World War 11, the application of various spectroscopic and structural probes made it possible to investigate catalyst surfaces at a more microscopic level. Studies with idealized surfaces such as the faces of single crystals in ultra-high vacuum apparatus also made their appearance. By the end of the twentieth century, direct information was being obtained on the rates of elementary reactions of well-defined surface species. The results of such work are beginning to put "finishing touches" on the great insight of early pioneers in surface science and heterogeneous catalysis. Much has been accomplished, but exciting opportunities still remain. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:923 / 946
页数:24
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