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Journal articles
Towards organic film passivation of germanium wafers using diazonium salts: mechanism and ambient stability
Abstract : Germanium is well-known for its good electronic properties but also the poor passivation quality of its natural or thermally-grown oxide layer. The robust passivation of Ge surfaces is thus a crucial step on the way to its integration in electronics at nanoscale. Before passivation, the natural oxide layer must be removed from the surface. Different methods were investigated and compared. The surfaces were analyzed by X-ray photoelectron spectroscopy and by atomic force microscopy to determine the impact of the etching on the roughness. Oxide-free Cl-terminated surfaces were chosen and functionalized with various arenediazonium salts. The grafting is a fast reaction (less than 30 minutes) and proceeds in soft conditions (room temperature in acetonitrile solutions). The functionalization was found to proceed even at low temperature (-18°C). The modified surfaces were mainly studied by XPS and AFM. The morphology of the organic layer was influenced by the temperature and duration of the grafting as well as by the presence of substituents on the aromatic ring. We demonstrated that smooth oxide-free Ge surfaces could be prepared by a cyclic oxidation- rinsing- etching procedure and could be functionalized with various arenediazonium salts. The stability of the organic layer was compared to the stability of a self-assembled monolayer of alkanethiolates. The absolute coverage was also determined. This constitutes a first step towards Ge crystal passivation by organic thin films.
https://hal-cea.archives-ouvertes.fr/cea-00960577
Contributor : Serge Palacin Connect in order to contact the contributor
Submitted on : Tuesday, March 18, 2014 - 1:56:59 PM
Last modification on : Wednesday, July 15, 2020 - 9:34:02 AM
Contributor : Serge Palacin Connect in order to contact the contributor
Submitted on : Tuesday, March 18, 2014 - 1:56:59 PM
Last modification on : Wednesday, July 15, 2020 - 9:34:02 AM