hide
Free keywords:
Alcohols; Silicon; Synchrotron radiation photoelectron spectroscopy; Surface chemical reaction
Abstract:
The adsorption of 2,3-butanediol on a Si(1 0 0) surface has been investigated by photoelectron spectroscopy. The valence band spectra show features assigned to molecular orbitals of 2,3-butanediol by comparison with calculations, and the surface states of clean Si are removed. The Si 2p reveals core-level shifts with two new components at 0.24 and 0.97 eV from the bulk, which are assigned to Si–H and Si–O bonds, respectively. The C 1s core-level spectrum consists of two major peaks separated by 1.3 eV, which are attributed to carbon atoms in –CHOH and –CH3 groups, in the molecule respectively. From the analysis of the valence band, the Si 2p, C 1s, and O 1s core-level spectra, we conclude that the 2,3-butanediol molecule undergoes a cleavage of the O–H bonds, and is bonded to the surface by the oxygen atoms. The molecule shows no further fragmentation and probably forms a six-membered ring of the O–C–C–O segment with the Si dimer atoms.
