Second-harmonic spectroscopy of a Si(001) surface during calibrated variations in temperature and hydrogen coverage

被引:79
作者
Dadap, JI
Xu, Z
Hu, XF
Downer, MC
Russell, NM
Ekerdt, JG
Aktsipetrov, OA
机构
[1] UNIV TEXAS,DEPT PHYS,SCI & TECHNOL CTR SYNTH GROWTH & ANAL ELECT MAT,AUSTIN,TX 78712
[2] UNIV TEXAS,DEPT CHEM ENGN,SCI & TECHNOL CTR SYNTH GROWTH & ANAL ELECT MAT,AUSTIN,TX 78712
[3] MOSCOW MV LOMONOSOV STATE UNIV,DEPT PHYS,MOSCOW 119899,RUSSIA
来源
PHYSICAL REVIEW B | 1997年 / 56卷 / 20期
关键词
D O I
10.1103/PhysRevB.56.13367
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The epitaxial growth of silicon films by chemical vapor deposition (CVD) is strongly affected by temperature and hydrogen (H) termination. We report measurements of p-polarized optical second-harmonic (SH) spectra generated in reflection from clean 2x1-reconstructed and H-terminated epitaxial Si(001) surfaces with no intentional doping by Ti:sapphire femtosecond laser pulses for SH photon energies 3.0 less than or equal to 2 (h) over bar omega less than or equal to 3.5 eV near the bull; E-1 resonance. Temperatures were varied from 200 to 900 K and H coverages from 0 to 1.5 monolayers (ML). Increases in temperature at fixed I-I-coverage redshift and broaden the E-1 resonance, as observed in linear bulk spectroscopy. Increases in H coverage from 0 to 1 ML at fixed temperature strongly quench, redshift, and distort the lineshape of the E-1 resonance even though reflection high-energy electron diffraction shows that the surface maintains the dimerized 2x1 reconstruction. The latter spectroscopic variations cannot be explained by vertical strain relaxation in the selvedge region, nor by bulk electric-field-induced SH (EFISH) effects. We instead attribute these variations to a monohydride-induced surface chemical modification, which we parametrize as a surface EFISH effect because submonolayer H strongly alters surface electric fields by redistributing charge from surface dimers into the bulk. The effects of vertical strain relaxation are weakly evident as a blueshift of the E-1 resonance accompanying dihydride termination (1.0-1.5 ML), which breaks the surface dimer bond. This modification is parametrized as a separate field-independent alteration to the surface dipole susceptibility chi(surface)((2)). Finally, guided by these SH spectroscopic studies, we demonstrate dynamic real-time (100-ms resolution) SH monitoring of H coverage (5% accuracy) during temperature programmed hydrogen desorption and CVD epitaxial growth of silicon from disilane.
引用
收藏
页码:13367 / 13379
页数:13
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