The Effect of Temperature and Si Concentration on the Mixing of AlAs/GaAs Superlattices

1986 ◽  
Vol 77 ◽  
Author(s):  
Ping Mei ◽  
H. W. Yoon ◽  
T. Venkatesan ◽  
S. A. Schwarz ◽  
J. P. Harbison

ABSTRACTThe intermixing of AlAs/GaAs superlattices has been investigated as a function of Si concentration following anneals in the range of 500 to 900 C. The superlattice samples were grown by molecular beam epitaxy(MBE) and the near surface layers were doped with silicon at concentrations of 2×10 to 5×1018 cm-3. Si and Al depth profiles were measured with secondary ion mass spectrometry (SIMS).The diffusion length and activation energy of Al as a function of silicon dopant concentration are derived from the SIMS data. In the temperature range studied an activation energy for the Al interdiffusion of -4eV is observed with the diffusion coefficients increasing rapidly with Si concentration.

Author(s):  
S. H. Chen

Sn has been used extensively as an n-type dopant in GaAs grown by molecular-beam epitaxy (MBE). The surface accumulation of Sn during the growth of Sn-doped GaAs has been observed by several investigators. It is still not clear whether the accumulation of Sn is a kinetically hindered process, as proposed first by Wood and Joyce, or surface segregation due to thermodynamic factors. The proposed donor-incorporation mechanisms were based on experimental results from such techniques as secondary ion mass spectrometry, Auger electron spectroscopy, and C-V measurements. In the present study, electron microscopy was used in combination with cross-section specimen preparation. The information on the morphology and microstructure of the surface accumulation can be obtained in a fine scale and may confirm several suggestions from indirect experimental evidence in the previous studies.


1988 ◽  
Vol 144 ◽  
Author(s):  
Samuel Chen ◽  
S.-Tong Lee ◽  
G. Braunstein ◽  
G. Rajeswaran

ABSTRACTLayer intermixing in MeV Si-implanted quantum well superlattices (SLs) has been studied by transmission electron microscopy, secondary ion mass spectrometry and Rutherford backscattering spectroscopy. Molecular beam epitaxially grown GaAs(200Å) - Al0. 5Ga0.5As(200Å) SLs were implanted with 1 MeV Si+ at doses between 3 × 1014 and 1 × 1016/cm2. The implanted SLs were either furnace annealed at 850°C for 3 hr or rapid thermally annealed at 1050°C for 10 sec, both under GaAs proximity capping conditions. Totally mixed regions were observed only for the SLs implanted with 1 × 1016 Si/cm2 and then furnace annealed at 850°C for 3 hr. For the same dose, the RTA annealed SLs only showed slight layer intermixing. At lower doses, no appreciable intermixing was detected in either furnace or RTA annealed samples. By contrast, under either annealing condition extensive intermixing has been demonstrated for lower energy (220 keV) implantation, but at doses almost two orders of magnitude lowerl XTEM showed that in all the annealed samples, a defect-free zone existed in the near-surface region, followed by a band of secondary defects, with the maximum density located at about 1 μm below the surface. In the disordered samples, the position of the intermixed layers correlated with the defect band maximum. Under both annealing conditions, Si concentration profiles only showed slight broadening, and they correlated with the distribution of secondary defects as well as with the depth of the intermixed layers. The effects of dynamic annealing and surface on the implantation energy dependence, i.e., MeV vs. keV, of layer intermixing are discussed.


1999 ◽  
Vol 568 ◽  
Author(s):  
L. Kappius ◽  
A. K. Tyagi ◽  
U. Breuer ◽  
H. L. Bay ◽  
S. Manti

ABSTRACTWe have studied the influence of an epitaxial silicide layer on the diffusion of B and Sb in silicon. B and Sb doping superlattices have been grown by molecular beam epitaxy. They were then covered with a 20 nm thick CoSi2 layer. Test samples were also grown without silicide. Samples were oxidized at various temperatures ranging from 800°C to 1200°C for times that ensured sufficient broadening of the spikes. Another set of samples was annealed at the same times and temperatures in N2. Dopant depth profiles were measured before and after diffusion by secondary ion mass spectrometry (SIMS). At the test samples we observed thermal diffusion of B and Sb, oxidation enhanced diffusion of B and oxidation retarded diffusion of Sb, all in accordance with the literature. In contrast to this, oxidized silicide capped samples showed a retardation of B diffusion by a factor of 2 - 10 as compared to thermal diffusivity and an enhancement of Sb diffusion by a factor of 1 - 2.


1992 ◽  
Vol 262 ◽  
Author(s):  
J.W. Honeycutt ◽  
J. Ravi ◽  
G. A. Rozgonyi

ABSTRACTThe effects of Ti and Co silicidation on P+ ion implantation damage in Si have been investigated. After silicidation of unannealed 40 keV, 2×1015 cm-2 P+ implanted junctions by rapid thermal annealing at 900°C for 10–300 seconds, secondary ion mass spectrometry depth profiles of phosphorus in suicided and non-silicided junctions were compared. While non-silicided and TiSi2 suicided junctions exhibited equal amounts of transient enhanced diffusion behavior, the junction depths under COSi2 were significantly shallower. End-of-range interstitial dislocation loops in the same suicided and non-silicided junctions were studied by planview transmission electron microscopy. The loops were found to be stable after 900°C, 5 minute annealing in non-silicided material, and their formation was only slightly effected by TiSi2 or COSi2 silicidation. However, enhanced dissolution of the loops was observed under both TiSi2 and COSi2, with essentially complete removal of the defects under COSi2 after 5 minutes at 900°C. The observed diffusion and defect behavior strongly suggest that implantation damage induced excess interstitial concentrations are significantly reduced by the formation and presence of COSi2, and to a lesser extent by TiSi2. The observed time-dependent defect removal under the suicide films suggests that vacancy injection and/or interstitial absorption by the suicide film continues long after the suicide chemical reaction is complete.


1999 ◽  
Vol 560 ◽  
Author(s):  
Lily H. Zhang ◽  
Larry Wang ◽  
Wusheng Tong ◽  
YongBao Xin

ABSTRACTThis study has used secondary ion mass spectrometry (SIMS) as a technique for thin film EL material characterization. It has shown that the Cu dopant concentration in the SrS films directly correlates with the luminescent brightness of the EL devices. A series of SrS:Cu,Y were grown using MBE to study the Y co-doping effects. It has been found that Y peak concentration and areal density in the SrS increased as the Y evaporation cell temperature was increased. The maximum PL intensity was found in the sample grown in the middle of the Y cell temperature range used. The Y co-doping has shown to reduce the thermal quenching effects in SrS EL devices. Therefore, in this series of samples, a good correlation has been found between Y and Cu concentration and the EL device performance characteristics.


2009 ◽  
Vol 1201 ◽  
Author(s):  
Pekka Tapio Neuvonen ◽  
Lasse Vines ◽  
Klaus Magnus Johansen ◽  
Anders Hallén ◽  
Bengt Gunnar Svensson ◽  
...  

AbstractSecondary ion mass spectrometry has been applied to study the transportation of Na and Li in hydrothermally grown ZnO. A dose of 1015 cm-2 of Na+ was implanted into ZnO to act as a diffusion source. A clear trap limited diffusion is observed at temperatures above 550 °C. From these profiles, an activation energy for the transport of Na of ∼1.7 eV has been extracted. The prefactor for the diffusion constant and the solid solubility of Na cannot be deduced independently from the present data but their product estimated to be ∼3 × 1016 cm-1s-1. A dissociation energy of ∼2.4 eV is extracted for the trapped Na. The measured Na and Li profiles show that Li and Na compete for the same traps and interact in a way that Li is depleted from Na-rich regions. This is attributed to a lower formation energy of Na-on-zinc-site than that for Li-on-zinc-site defects and the zinc vacancy is considered as a major trap for migrating Na and Li atoms. Consequently, the diffusivity of Li is difficult to extract accurately from the present data, but in its interstitial configuration Li is indeed highly mobile having a diffusivity in excess of 10-11 cm2s-1 at 500 °C.


Author(s):  
М.Н. Дроздов ◽  
Ю.Н. Дроздов ◽  
А.И. Охапкин ◽  
С.А. Краев ◽  
М.А. Лобаев

AbstractNew possibilities offered by the method of secondary ion mass spectrometry (SIMS) for analysis of the phase composition of carbon-containing materials are considered. Differences are established between the mass spectra of three carbon phases: diamond, diamond-like carbon (DLC), and graphite. A simple algorithm for the quantitative determination of different phases in two-phase systems diamond–graphite and DLC–graphite is proposed that is based on the measurement of relative intensities of secondary cluster ions such as C_8/C_5 and CsC_8/CsC_4. It is shown that nonuniform depth profiles of various carbon phases are formed in diamond structures upon laser cutting and in DLC structures upon thermal annealing.


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