THE ROLE OF HYDRIDE COVERAGE IN SURFACE-LIMITED THIN-FILM GROWTH OF EPITAXIAL SILICON AND GERMANIUM

被引:23
作者
ERES, G
SHARP, JW
机构
[1] Oak Ridge National Laboratory, Solid State Division, MS 6056, Oak Ridge, TN 378331-6056
关键词
D O I
10.1063/1.355014
中图分类号
O59 [应用物理学];
学科分类号
摘要
The connection between the hydride coverage and thin-film growth rate was investigated by a kinetic model consisting of the elementary reaction steps of source gas chemisorption and hydrogen desorption in silicon and germanium epitaxial thin-film growth from silanes and germanes. A generalized form of the model for steady-state conditions was used to extract the kinetic parameters of the elementary reaction steps from experimental film growth data in the literature. Three-dimensional plots of the growth rate as a function of the substrate temperature and the source gas flux were used to summarize the trends in steady-state surface-limited thin-film growth using the kinetic parameters extracted by the model. The three-dimensional plots show that: (1) each of the elementary reaction steps is dominantly dependent only on a single external growth parameter, and (2) in the transition region where neither of the elementary steps is clearly dominant the growth rates exhibit a complex dependenee on the growth parameters. The kinetic parameters for the elementary reaction steps are found to be in good agreement with the values obtained by independent (nonfilm growth) surface studies. The insight gained by modeling the hydride coverage in thin-film growth led to development of digital epitaxy, an alternative growth method to atomic layer epitaxy of group IV materials. Digital epitaxy is accomplished through cyclic repetition of alternating chemisorption and hydrogen desorption stages.
引用
收藏
页码:7241 / 7250
页数:10
相关论文
共 52 条
[1]   LIMITATIONS OF SELECTIVE EPITAXIAL-GROWTH CONDITIONS IN GAS-SOURCE MBE USING SI2H6 [J].
AKETAGAWA, K ;
TATSUMI, T ;
SAKAI, J .
JOURNAL OF CRYSTAL GROWTH, 1991, 111 (1-4) :860-863
[2]  
ANDERSON JB, 1965, ADV ATOM MOL PHYS, P345
[3]  
Baladin A. A., 1969, ADV CATAL, V19, P1, DOI DOI 10.1016/S0360-0564(08)60029-2
[4]   TEMPERATURE-DEPENDENCE OF THE GROWTH-RATE OF SILICON PREPARED THROUGH CHEMICAL VAPOR-DEPOSITION FROM SILANE [J].
BEERS, AM ;
BLOEM, J .
APPLIED PHYSICS LETTERS, 1982, 41 (02) :153-155
[5]  
BENSON SW, 1960, F CHEM KINETICS, P26
[6]   SCANNING TUNNELING MICROSCOPY STUDY OF THE ADSORPTION AND RECOMBINATIVE DESORPTION OF HYDROGEN FROM THE SI(100)-2X1 SURFACE [J].
BOLAND, JJ .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1992, 10 (04) :2458-2464
[7]   EVIDENCE OF PAIRING AND ITS ROLE IN THE RECOMBINATIVE DESORPTION OF HYDROGEN FROM THE SI(100)-2X1 SURFACE [J].
BOLAND, JJ .
PHYSICAL REVIEW LETTERS, 1991, 67 (12) :1539-1542
[8]   THERMAL AND ELECTRON-BEAM-INDUCED REACTION OF DISILANE ON SI(100)-(2X1) [J].
BOZSO, F ;
AVOURIS, P .
PHYSICAL REVIEW B, 1988, 38 (06) :3943-3947
[9]   REACTIVE STICKING COEFFICIENTS FOR SILANE AND DISILANE ON POLYCRYSTALLINE SILICON [J].
BUSS, RJ ;
HO, P ;
BREILAND, WG ;
COLTRIN, ME .
JOURNAL OF APPLIED PHYSICS, 1988, 63 (08) :2808-2819
[10]   ADSORPTION AND DECOMPOSITION OF HYDRIDES ON GE(100) [J].
COHEN, SM ;
YANG, YML ;
ROUCHOUZE, E ;
JIN, T ;
DEVELYN, MP .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1992, 10 (04) :2166-2171