Chemical reactions of water molecules on Ru(0001) induced by selective excitation of vibrational modes

被引:16
作者
Mugarza, Aitor [1 ,2 ]
Shimizu, Tomoko K. [1 ,3 ]
Ogletree, D. Frank [1 ]
Salmeron, Miquel [1 ,3 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
[2] CSIC, Inst Ciencia Mat Barcelona, Bellaterra 08193, Spain
[3] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
关键词
Scanning tunneling microscopy; SCANNING TUNNELING MICROSCOPE; DISSOCIATIVE ADSORPTION; SINGLE-MOLECULE; SURFACE; MANIPULATION; DIFFUSION; STABILITY; COVERAGE; PD(111); CU(110);
D O I
10.1016/j.susc.2009.03.026
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
Tunneling electrons in a scanning tunneling microscope were used to excite specific vibrational quantum states of adsorbed water and hydroxyl molecules on a Ru(0 0 0 1) surface. The excited molecules relaxed by transfer of energy to lower energy modes, resulting in diffusion, dissociation, desorption, and surface-tip transfer processes. Diffusion of H2O molecules could be induced by excitation of the O-H stretch vibration mode at 445 meV. Isolated molecules required excitation of one single quantum while molecules bonded to a C atom required at least two quanta. Dissociation of single H2O molecules into H and OH required electron energies of 1 eV or higher while dissociation of OH required at least 2 eV electrons. In contrast, water molecules forming part of a cluster could be dissociated with electron energies of 0.5 eV. Published by Elsevier B.V.
引用
收藏
页码:2030 / 2036
页数:7
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