We present preliminary results of an experimental investigation of ordered phases of CH3S chemisorbed on Au(111). The self-assembled monolayer has been grown by dosing dimethyl disulfide in ultrahigh vacuum at different substrate temperatures between 200 K and 320 K and following different protocols. The monolayers have been characterized by means of low-energy He atom scattering with time-of-flight detection in a temperature range between 150 K and 300 K. The observed diffraction patterns show that the main periodicity is well-described by the (3 x 4) overlayer of the Au(111) lattice, coexisting with the (root 3 x root 3) periodicity, in agreement with previous results obtained by means of low-energy electron diffraction.
Structural study of CH3S self-assembled monolayers on Au(111) / Bracco, G; Cavanna, D; Thea, S.; DE RENZI, Valentina. - In: VACUUM. - ISSN 0042-207X. - STAMPA. - 82:12(2008), pp. 1421-1424. [10.1016/j.vacuum.2008.03.017]
Structural study of CH3S self-assembled monolayers on Au(111)
DE RENZI, Valentina
2008
Abstract
We present preliminary results of an experimental investigation of ordered phases of CH3S chemisorbed on Au(111). The self-assembled monolayer has been grown by dosing dimethyl disulfide in ultrahigh vacuum at different substrate temperatures between 200 K and 320 K and following different protocols. The monolayers have been characterized by means of low-energy He atom scattering with time-of-flight detection in a temperature range between 150 K and 300 K. The observed diffraction patterns show that the main periodicity is well-described by the (3 x 4) overlayer of the Au(111) lattice, coexisting with the (root 3 x root 3) periodicity, in agreement with previous results obtained by means of low-energy electron diffraction.Pubblicazioni consigliate
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris