ELECTRON SPECTROSCOPIC ANALYSIS OF THE SIO2 SI SYSTEM AND CORRELATIONWITH METAL-OXIDE-SEMICONDUCTOR DEVICE CHARACTERISTICS/

Citation
S. Iwata et A. Ishizaka, ELECTRON SPECTROSCOPIC ANALYSIS OF THE SIO2 SI SYSTEM AND CORRELATIONWITH METAL-OXIDE-SEMICONDUCTOR DEVICE CHARACTERISTICS/, Journal of applied physics, 79(9), 1996, pp. 6653-6713
Citations number
261
Categorie Soggetti
Physics, Applied
Journal title
ISSN journal
00218979
Volume
79
Issue
9
Year of publication
1996
Pages
6653 - 6713
Database
ISI
SICI code
0021-8979(1996)79:9<6653:ESAOTS>2.0.ZU;2-R
Abstract
ESCA (electron spectroscopy for chemical analysis) measurement results on thin SiO2/Si samples are examined comprehensively, critically, and in detail to show that it is possible to correlate these results with MOS (metal-oxide-semiconductor) device characteristics such as flatba nd (threshold) voltage, oxide breakdown field, mobile-ion density, hol e and electron trap density, and hot-carrier lifetime. Up to now, much effort has been made to detect SiO2 phases at SiO2/Si interfaces sinc e they are thought to have a significant effect on MOS device characte ristics. However, correlating the SiO2 phases with device characterist ics is difficult and involves overcoming two problems. First, the chem ical state is difficult to determine exactly due to x-ray-irradiation effects. Second, the amount of defects and impurities which influence device characteristics is usually below the ESCA detection limit (10(1 2)-10(13) cm(-2)) in device-quality SiO2/Si samples. Investigation of the first problem led to the conclusion that it is possible to correct for these effects from the x-ray intensity or oxide thickness depende nce of the chemical shift. However, accurate (better than +/-0.2 eV) c hemical state determination is not easy. It is therefore necessary to approach this detection problem from a different viewpoint. Our first attempt involves measuring the ESCA thickness, which decreases when ox ide defects like unoxidized Si or uneven thickness (or pinholes) are p resent, resulting in breakdown field degradation. Our second attempt s tarted while we were studying how to interpret the measured chemical s hift. The photoelectron peaks of the SiO2 and the Si can be observed t o shift due to small amounts of charged defects and impurities; althou gh they cannot be detected as peaks. This method is considered to be e specially useful for characterizing ultrathin (a few mn thick) SiO2/Si samples which are difficult to characterize using conventional C-V (c apacitance-voltage) measurements because of tunneling currents. Accord ingly, we discuss the data obtained in steady-state and transient peak position measurements of SiO2/Si samples containing 10(10)-10(12) cm( -2) of Na (sodium) ions, 10(12)-10(13) cm(-2) of hole and electron tra ps, and 10(14)-10(21) cm(-3) of impurities such as P (phosphorus) (in the Si). It is shown that a correlation with MOS characteristics is po ssible. A close scrutiny of various results concerning x-ray irradiati on time, intensity, and oxide thickness dependence of the above peak p ositions indicates that electric charging during ESCA measurements is correlated to the trap-capturing process. As MOS characteristics are a lso related to this process, more studies in this direction are needed and will certainly yield more information on the defects influencing the MOS characteristics and the trap-capturing mechanism. (C) 1996 Ame rican Institute of Physics.