The evolution of surface chemistry. A personal view of building the future on past and present accomplishments

被引:46
作者
Somorjai, GA [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
关键词
D O I
10.1021/jp0209751
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
Surface chemistry, like other branches of physical chemistry, historically developed through macrosopic studies. These included measurements of adsorption-desorption equilibria (adsorption isotherms), spreading of monomolecular films, surface dissociation of diatomic molecules, and kinetic studies of desorption, sticking, and catalytic oxidation of CO and H-2. Models of surface structures were proposed by Langmuir and Taylor on the bases of experimental findings. Molecular level studies of surface chemistry were delayed as compared to other fields of physical chemistry until the late 1950s as instrumentation to detect properties of the very small number of surface atoms (10(15) cm(-2)) in the presence of a large number of bulk atoms (10(22) cm(-3)) were not available. At present we have over 65 techniques (photon, electron, molecule, and ion scattering, and scanning probes) that can investigate composition, atomic and electronic structures, and the dynamics of their motion with less than or equal to1% of a monolayer sensitivity. Key results include: quantitative determinations of surface segregation of constituents that minimize surface free energy, discovery of clean surface reconstruction and adsorbate induced restructuring, and the uniquely high chemical activity of rough surfaces and defects (steps and kinks). In situ molecular studies during surface reaction reveal the need for restructuring of metal surface atoms by a highly mobile strongly adsorbed overlayer to maintain catalytic activity: additives that inhibit mobility on the surface poison chemical reactivity. New techniques permitting molecular surface studies at high pressures and at solid-liquid interfaces greatly accelerated the developments of molecular surface chemistry and permitted in situ studies of complex surface chemical phenomena: catalytic reactions, electrode surface chemistry, and polymer surfaces. As always, further developments of techniques control the rate of progress of molecular surface chemistry.
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页码:9201 / 9213
页数:13
相关论文
共 95 条
[31]   DIRECT LOW-ENERGY ELECTRON-DIFFRACTION ANALYSIS OF C(2X2)O/NI(100) INCLUDING SUBSTRATE RECONSTRUCTION [J].
HEINZ, K ;
OED, W ;
PENDRY, JB .
PHYSICAL REVIEW B, 1990, 41 (14) :10179-10181
[32]   THE STRUCTURE SENSITIVITY OF CYCLOHEXANE DEHYDROGENATION AND HYDROGENOLYSIS CATALYZED BY PLATINUM SINGLE-CRYSTALS AT ATMOSPHERIC-PRESSURE [J].
HERZ, RK ;
GILLESPIE, WD ;
PETERSEN, EE ;
SOMORJAI, GA .
JOURNAL OF CATALYSIS, 1981, 67 (02) :371-386
[33]  
Horiuti J., 1934, Transactions ofthe Faraday Society, V30, P1164, DOI DOI 10.1039/TF9343001164
[34]   REACTIONS OF CARBON-MONOXIDE AT COORDINATIVELY UNSATURATED SITES ON A PLATINUM SURFACE [J].
IWASAWA, Y ;
MASON, R ;
TEXTOR, M ;
SOMORJAI, GA .
CHEMICAL PHYSICS LETTERS, 1976, 44 (03) :468-470
[35]   High pressure, high temperature scanning tunneling microscopy [J].
Jensen, JA ;
Rider, KB ;
Chen, Y ;
Salmeron, M ;
Somorjai, GA .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY B, 1999, 17 (03) :1080-1084
[36]   The dissociation of hydrogen into atoms [Part II] Calculation of the degree of dissociation and the heat of formation [J].
Langmuir, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1915, 37 :417-458
[37]   A chemically active modification of hydrogen. [J].
Langmuir, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1912, 34 :1310-1325
[38]   The dissociation of hydrogen into atoms - III - The mechanism of the reaction [J].
Langmuir, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1916, 38 :1145-1156
[39]   Chemical reactions at very low pressures. II. The chemical clean-up of nitrogen in a tungsten lamp. [J].
Langmuir, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1913, 35 :931-945
[40]   The dissociation of hydrogen into atoms. [J].
Langmuir, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1912, 34 :860-877