Photochemistry of N2O on Si(100), surface photo-oxidation

被引:11
作者
Kato, H
Lee, J
Sawabe, K
Matsumoto, Y [1 ]
机构
[1] Inst Mol Sci, Okazaki, Aichi 4448585, Japan
[2] Grad Univ Adv Studies, Sch Adv Sci, Dept Photosci, SOKEN,DAI, Kanagawa 2400193, Japan
[3] Seoul Natl Univ, Dept Chem Technol, Seoul 151742, South Korea
基金
日本学术振兴会;
关键词
desorption induced by electronic transitions; nitrogen oxides; oxidation; silicon; surface photochemistry;
D O I
10.1016/S0039-6028(99)01043-2
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
The oxidation of an Si(100) surface induced by photodissociation of adsorbed N2O has been studied by X-ray photoelectron spectroscopy, temperature-programmed desorption, and angle-resolved time-of-flight (TOF) measurements. N2O adsorbs in physisorption and chemisorption states on Si(100), The photochemical oxidation is induced by the irradiation of light in the wavelength range between 532 and 193 nm, The cross-sections of both adsorption states at 193 nm are larger than that of gaseous N2O by about two orders of magnitude. Substrate-mediated excitation is considered to be responsible for the photochemistry of N2O in the two adsorption states. Although the TOF distributions of N-2 fragments from the physisorbed N2O are almost identical in the wavelength region studied, those from the chemisorbed N2O show a marked wavelength dependence. The interpretation is that there are multiple types of chemisorbed states whose photodissociation dynamics and the wavelength dependence of the cross-section are different to each other. (C) 2000 Elsevier Science B,V, All rights reserved.
引用
收藏
页码:209 / 223
页数:15
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