Please use this identifier to cite or link to this item:
https://scholarbank.nus.edu.sg/handle/10635/113229
Title: | Auger electron spectroscopy and x-ray photoelectron spectroscopy analysis of angle of incidence effects of ion beam nitridation of GaAs | Authors: | Pan, J.S. Huan, C.H.A. Wee, A.T.S. Tan, H.S. Tan, K.L. |
Issue Date: | Jul-1998 | Citation: | Pan, J.S.,Huan, C.H.A.,Wee, A.T.S.,Tan, H.S.,Tan, K.L. (1998-07). Auger electron spectroscopy and x-ray photoelectron spectroscopy analysis of angle of incidence effects of ion beam nitridation of GaAs. Journal of Materials Research 13 (7) : 1799-1807. ScholarBank@NUS Repository. | Abstract: | Ion beam nitridation (IBN) of GaAs at room temperature was studied as a function of N2 + ion incident angle at ion energy of 10 keV. The ion beam bombardment surface area of GaAs was characterized in situ by both Auger electron spectroscopy (AES) and small spot-size x-ray photoelectron spectroscopy (XPS). Thin GaN reaction layers are formed at all N2 + ion incident angles, whereas the formation of As-N bonds has not been found. However, the degree of nitridation of Ga decreases with increasing incident angle. The observed angular dependence of the N incorporation can be explained in terms of sputtering yield, indicating that the growth kinetics can be described as a dynamic process comprising the accumulation of N and sputter removal of the surface layer. N2 + ion bombardment causes the depletion of As from the surface region because of the preferential sputtering of As from GaAs. The preferential sputtering of As reduces with increasing N2 + ion incident angle. The angular dependent behavior of preferential sputtering of As by 10 keV N2 + ions can be attributed to the angular dependence of GaN surface layer formation. | Source Title: | Journal of Materials Research | URI: | http://scholarbank.nus.edu.sg/handle/10635/113229 | ISSN: | 08842914 |
Appears in Collections: | Staff Publications |
Show full item record
Files in This Item:
There are no files associated with this item.
Google ScholarTM
Check
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.