Non-adiabaticity in surface chemical reactions

被引:34
作者
Hasselbrink, Eckart [1 ,2 ]
机构
[1] Univ Duisburg Essen, Fachbereich Chem, D-45117 Essen, Germany
[2] Univ Duisburg Essen, Ctr Nanointegrat CeNIDE, D-45117 Essen, Germany
关键词
Energy dissipation; Non-adiabaticity; Pt; Au; Metal-insulator-metal contact; Adsorption; Recombinative desorption; HOLE PAIR EXCITATIONS; METAL-SURFACES; ELECTRONIC EXCITATIONS; ATOMIC-HYDROGEN; ELEY-RIDEAL; HOT-ATOM; REACTION-PRODUCTS; CU(111) SURFACES; CO OXIDATION; H(D) ATOMS;
D O I
10.1016/j.susc.2008.12.037
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
Chemical reactions at surface may dissipate energy exciting electron-hole pairs in the metal substrate. Direct detection of the chemically induced hot charge carriers may be achieved by measuring the tunnel current in Ta-TaOx-Au tunnel junctions when the Au top electrode is exposed to an atomic hydrogen beam. A current of 1 nA cm(-2) Was observed during a hydrogen exposure with a flux of 0.1 ML s(-1). The transient is related to the reaction kinetics and allows us to identify the elementary reaction steps causing the electronic excitations which are monitored by the observed current. Using Pt as top electrode material a markedly different transient is observed. Applying a bias voltage to the sensor allows spectroscopy of the electronic excitations. The experiments provide detailed insights into the non-adiabaticity of various reaction steps at a surface. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1564 / 1570
页数:7
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