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Luminescence and microstructure of Er/O co-doped Si structures grown by MBE using Er and SiO evaporation
Er and O co-doped Si structures have been prepared using molecular-beam epitaxy (MBE) with fluxes of Er and O obtained from Er and silicon monoxide (SiO) evaporation in high-temperature cells. The incorporation of Er and O has been studied for concentrations of up to 2×10 20 and 1×10 21 cm −3, respe...
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Published in: | Materials science in semiconductor processing 2000-10, Vol.3 (5), p.523-528 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Er and O co-doped Si structures have been prepared using molecular-beam epitaxy (MBE) with fluxes of Er and O obtained from Er and silicon monoxide (SiO) evaporation in high-temperature cells. The incorporation of Er and O has been studied for concentrations of up to 2×10
20 and 1×10
21
cm
−3, respectively. Surface segregation of Er can take place, but with O co-doping the segregation is suppressed and Er-doped layers without any indication of surface segregation can be prepared. Si
1−
x
Ge
x
and Si
1−
y
C
y
layers doped with Er/O during growth at different substrate temperatures show more defects than corresponding Si layers. Strong emission at 1.54
μm associated with the intra-4f transition of Er
3+ ions is observed in electroluminescence (EL) at room temperature in reverse-biased p–i–n-junctions. To optimize the EL intensity we have varied the Er/O ratio and the temperature during growth of the Er/O-doped layer. Using an Er-concentration of around 1×10
20
cm
−3 we find that Er/O ratios of 1
:
2 or 1
:
4 give higher intensity than 1
:
1 while the stability with respect to breakdown is reduced for the highest used O concentrations. For increasing growth temperatures in the range 400–575°C there is an increase in the EL intensity. A positive effect of post-annealing on the photoluminescence intensity has also been observed. |
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ISSN: | 1369-8001 1873-4081 1873-4081 |
DOI: | 10.1016/S1369-8001(00)00075-5 |