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INTRODUCTION
A lot of progress has been made on the fabrication
of solid-state light emitters; however, there is a spec-
tral gap in the green-yellow region (530–590 nm) for
all commercially available devices.1
This spectral re-
gion is important for many emerging applications,
such as the use of plastic-optical fibers, that require
green lasers to achieve the lowest attenuation coeffi-
cient.2
Thus, ZnSe-based devices are still of high in-
terest because, in principle, they can cover the whole
spectral region between 490–590 nm. However, suc-
cessful production of bright, “long-lived” laser diodes
and light-emitting diodes is tempered by the lack of
good p-type ZnSe, among other problems.3
The use
of the ZnSe-Te system for improving the p-type dop-
ing has been suggested because ZnTe is easily doped
p-type. The best results so far within such an ap-
proach have been obtained by Jung et al.,4
who have
reported hole concentrations up to 7 ϫ 1018
cmϪ3
by
using a ␦-doped ZnSe/ZnTe:N superlattice. However,
because of a large lattice mismatch between the
ZnSe and ZnTe (ϳ7.4%), such a structure tends to
form defects, for instance, dislocations,5
that are
detrimental to device operation.
Recently,6
the use of a planar (␦-) doping tech-
nique has been suggested to reduce the average Te
content in the material. In such an approach, ZnSe
is codoped with Te and N in delta layers (which do
not form full ZnTe monolayers), separated by un-
doped-ZnSe spacers.6
The highest achieved net-ac-
ceptor concentration (NA Ϫ ND) is ϳ6 ϫ 1018
cmϪ3
with an average Te concentration of Ͻ1.8% (Table
I).7
In this paper, we report results of photolumines-
cence (PL) studies of ␦-doped ZnSe with very low Te
content but otherwise similar to previously reported
samples. We studied two types of samples: the so-
called single ␦-doped (␦-doping) and triple ␦-doped
(␦3
-doping), both of which have Te concentrations as
low as about 0.5%.
GROWTH AND DOPING
Growth was performed in a Riber 2300 molecular
beam epitaxy system in city college of CUNY.
Atomic N was produced by a radio-frequency dis-
charge N source. All samples were grown on (001) p-
type GaAs substrates. The present samples, prior to
the growth of the delta region, have buffer layers of
uniformly N-doped ZnSe. The growth rate was about
0.8 ␮m/h. The shutter control sequence used during
the growth is described elsewhere.6
Two types of
samples were studied. One was single ␦-doped (sam-
ple A), where only a small enhancement in the net-
acceptor concentration was obtained; the other was
␦3
-doped (sample B), and a significant increase of
the net-acceptor concentration was obtained.
PHOTOLUMINESCENCE RESULTS
In Figs. 1 and 2, we show the PL from samples A
and B (both have Te content of ϳ0.5%). The PL from
both samples shifts to red with decreasing excitation
Journal of ELECTRONIC MATERIALS, Vol. 31, No. 7, 2002 Special Issue Paper
Heavily p-Type Doped ZnSe Using Te and N Codoping
Y. GU,1,3
IGOR L. KUSKOVSKY,1
G.F. NEUMARK,1
W. LIN,2
S.P. GUO,2
O. MAKSIMOV,2
and M.C. TAMARGO2
1.—Department of Applied Physics and Applied Mathematics, Columbia University, New York, NY
10027. 2.—Chemistry Department, City College of CUNY, New York, NY 10007. 3.—E-mail:
yg99@columbia.edu
We have studied photoluminescence (PL) of ZnSe samples codoped with Te and
N in ␦-layers. We have concluded that Te clusters are involved in the PL. We
also compared the PL data of samples with lower Te concentrations to those
with higher Te concentrations; the results corroborate the Te-cluster conclu-
sion.
Key words: ZnSe, Te clusters, photoluminescence, p-type
(Received October 3, 2001; accepted March 2, 2002)
799
intensity, with such a shift being considered a hall-
mark of a donor-acceptor pair (DAP) PL.8
The PL of
sample A shows a series of peaks at 2.686 eV, 2.655
eV, 2.625 eV, and 2.594 eV. These peaks are sepa-
rated by 30–31 meV, which is about the ZnSe longi-
tudinal-optical phonon energy.9
However, it is clear
from Fig. 1 that the intensity of the peak at 2.655 eV
does not scale with the intensity of the 2.686-eV
peak, which indicates that these two peaks are asso-
ciated, at least partly, with different centers. Also, we
note that the peak at 2.655 eV is in the 2.63–2.68-eV
energy range, where we have previously observed PL
caused by excitons bound to Te pairs and/or clusters.10
Therefore, we suggest that this 2.655-eV peak has
some contributions from the recombination of exci-
tons bound to such Te complexes. As to the 2.686-eV
peak, it is very close to the peak position of the “deep”
DAP emission in ZnSe:N.11
The current value is
slightly high, but the present system is expected to
have a relatively strong Coulomb shift because of
preferential DAP11
emission, which could account for
this. Furthermore, it can be seen that, at low-excita-
tion intensity, this sample shows a small broad
shoulder at around 2.42 eV (Fig. 3), which is in the
range of the peak position (2.487 eV) of excitons
bound to TenՆ3 clusters.10
Therefore, even though the
Te concentration is as low as 0.5% in this sample, it
still shows quite efficient Te-cluster-related PL. This
can be understood by considering the geometry of
our sample, which could result in relatively high Te
concentration in the ␦-doped layer.
As to sample B, it shows only one broad peak at
around 2.457 eV. As mentioned, this peak shifts to
red with decreasing excitation intensity. However,
2.457 eV is too deep for the “ordinary” DAP peaks in
ZnSe. Furthermore, as mentioned previously, this
peak is close to the one assigned to excitons bound to
TenՆ3 clusters. Therefore, we believe that, in addition
to N, Te clusters are also involved in this transition.
Previously, we reported PL spectra of another set
of ␦- and ␦3
-doped ZnSe:(N ϩ Te) samples12
with
800 Gu, Kuskovsky, Neumark, Lin, Guo, Maksimov, and Tamargo
Table I. The Net Acceptor Concentrations
Te
Samples and Spacer NA Ϫ ND Concentration
Doping (ML) (cm Ϫ3
) (%)
Uniform ZnSe:N N/A 3.0 ϫ 1017
N/A
␦-ZnSe:(N) N/A 5.6 ϫ 1017
N/A
␦-ZnSe:(Te, N) 10 1.5 ϫ 1017
ϳ0.5
␦3
-ZnSe:(Te, N) 12 4.0 ϫ 1017
Ͻ3
␦3
-ZnSe:(Te, N) 7 6.0 ϫ 1017
Ͻ1.8
Fig. 1. PL spectra of sample A at different excitation intensities at
T ϭ 10K.
Fig. 2. PL spectra of sample B at different excitation intensities at
T ϭ 10K.
Fig. 3. The PL spectra of sample A at low-excitation intensity.
higher Te concentrations (1.8% and 3%, respec-
tively). It is instructive to compare those results
with those of our new samples with less Te concen-
trations (0.5%). In Fig. 4, we plot the integrated in-
tensity versus the excitation intensity for each of
our new samples, which show one slope for sample A
(␦-doped) and two slopes for sample B (␦3
-doped). We
note that with our previous samples, there are two
distinct slopes for each of them. Because the only
difference between the new ␦-doped sample and the
previous one is the Te concentration, the difference
in slopes corroborates our conclusion that Te is in-
volved in the PL. Regarding the two-slope case, as
discussed in Refs. 12 and 13, the plots show two
slopes if two recombination paths are present. We,
thus, note that despite the low Te content of the new
sample, the ␦3
geometry still gives a large number of
Te complexes around the ␦3
-layer region, enough to
give two paths. We also note that the PL-peak posi-
tion of the new ␦3
-doped sample is higher than that
of the previous one. This could be due to the fact that
the previous ␦3
-doped sample has more TenՆ3 clus-
ters, or alternatively, a sufficiently high Te concen-
tration to change the bandgap for this effect to take
place.
SUMMARY
In summary, we employed a modulation-doping
technique that allowed us to achieve a net-acceptor
concentration as high as 6 ϫ 1018
cmϪ3
with Te less
than 1.8%. The low-temperature PL spectra of these
samples showed dominant Te-related peaks but also
involved N. We also compared the PL spectra of our
present samples (with lower Te concentrations) to
that of previous samples (with higher Te concentra-
tions). The results are consistent with our conclu-
sion that Te clusters are involved in the PL.
ACKNOWLEDGEMENT
The authors acknowledge the support of the De-
partment of Energy under Grant Nos. DE-FG02-
98ER45694 and DE-FG02-98ER45695.
REFERENCES
1. R. Haitz, F. Kish, J. Tsao, and J. Nelson, Comp. Semicond.
6, 34 (2000).
2. A. Weinert, Plastic Optical Fibers: Principles, Components,
Installation (Erlangen and Munich: Publicis MCD Verlag,
1999).
3. G.F. Neumark, Mater. Lett. 30, 131 (1997).
4. H.D. Jung, C.D. Song, S.Q. Wang, K. Arai, Y.H. Wu, Z. Zhu,
T. Yao, and H. Katayama-Yoshida, Appl. Phys. Lett. 70,
1143 (1997).
5. W. Faschinger, J. Nurnberger, E. Kurtz, R. Schmitt, M.
Korn, K. Schull, and M. Ehinger, Semicond. Sci. Technol.
12, 1291 (1997).
6. W. Lin, S.P. Guo, M.C. Tamargo, I.L. Kuskovsky, C. Tian,
and G.F. Neumark, Appl. Phys. Lett. 76, 2205 (2000).
7. I.L. Kuskovsky, Y. Gu, C. Tian, G.F. Neumark, S.P. Guo, W.
Lin, O. Maksimov, M.C. Tamargo, A.N. Alyoshin, and V.M.
Belous, Phys. Status Solidi (b) 229, 385 (2002).
8. J.I. Pankove, Optical Process in Semiconductor (New York:
Dover, 1974).
9. H. Hartman, R. Mach, and B. Selle, “Wide Gap II–VI Com-
pounds as Electronic Materials,” Current Topics in Materi-
als Science, vol. 9, ed. E. Kaldis (Amsterdam: North-Hol-
land, 1982).
10. I.L. Kuskovsky, C. Tian, G.F. Neumark, J.E. Spanier, I.P.
Herman, W. Lin, S.P. Guo, and M.C. Tamargo, Phys. Rev. B
63, 155205 (2001).
11. G.F. Neumark, L. Radomsky, and I. Kuskovsky, Proc. SPIE
2346, 159 (1994).
12. I.L. Kuskovsky, C. Tian, C. Sudbrack, G.F. Neumark, W.-C.
Lin, S.P. Guo, and M.C. Tamargo, J. Appl. Phys. 90, 2269
(2001).
13. V.V. Serdyuk, G.G. Chemeresyuk, and M. Terek, Photoelec-
trical Processes in Semiconductors (Kiev-Odessa: Vischa
Shkola, 1982) (in Russian).
Heavily p-Type Doped ZnSe Using Te and N Codoping 801
Fig. 4. The integrated PL intensity as a function of laser-excitation
intensity: (a) ␦-doped ZnSe:Te, N) and (b) ␦3
-doped ZnSe:(Te, N).
COPYRIGHT INFORMATION
TITLE: Heavily p-Type Doped ZnSe Using Te and N Codoping
SOURCE: J Electron Materns Part A 31 no722 Jl 20021998
The magazine publisher is the copyright holder of this article and it
is reproduced with permission. Further reproduction of this article in
violation of the copyright is prohibited. To contact the publisher:
http://www.springerlink.com/content/0361-5235/

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Heavily p-Type Doped ZnSe Using Te and N Codoping

  • 1. INTRODUCTION A lot of progress has been made on the fabrication of solid-state light emitters; however, there is a spec- tral gap in the green-yellow region (530–590 nm) for all commercially available devices.1 This spectral re- gion is important for many emerging applications, such as the use of plastic-optical fibers, that require green lasers to achieve the lowest attenuation coeffi- cient.2 Thus, ZnSe-based devices are still of high in- terest because, in principle, they can cover the whole spectral region between 490–590 nm. However, suc- cessful production of bright, “long-lived” laser diodes and light-emitting diodes is tempered by the lack of good p-type ZnSe, among other problems.3 The use of the ZnSe-Te system for improving the p-type dop- ing has been suggested because ZnTe is easily doped p-type. The best results so far within such an ap- proach have been obtained by Jung et al.,4 who have reported hole concentrations up to 7 ϫ 1018 cmϪ3 by using a ␦-doped ZnSe/ZnTe:N superlattice. However, because of a large lattice mismatch between the ZnSe and ZnTe (ϳ7.4%), such a structure tends to form defects, for instance, dislocations,5 that are detrimental to device operation. Recently,6 the use of a planar (␦-) doping tech- nique has been suggested to reduce the average Te content in the material. In such an approach, ZnSe is codoped with Te and N in delta layers (which do not form full ZnTe monolayers), separated by un- doped-ZnSe spacers.6 The highest achieved net-ac- ceptor concentration (NA Ϫ ND) is ϳ6 ϫ 1018 cmϪ3 with an average Te concentration of Ͻ1.8% (Table I).7 In this paper, we report results of photolumines- cence (PL) studies of ␦-doped ZnSe with very low Te content but otherwise similar to previously reported samples. We studied two types of samples: the so- called single ␦-doped (␦-doping) and triple ␦-doped (␦3 -doping), both of which have Te concentrations as low as about 0.5%. GROWTH AND DOPING Growth was performed in a Riber 2300 molecular beam epitaxy system in city college of CUNY. Atomic N was produced by a radio-frequency dis- charge N source. All samples were grown on (001) p- type GaAs substrates. The present samples, prior to the growth of the delta region, have buffer layers of uniformly N-doped ZnSe. The growth rate was about 0.8 ␮m/h. The shutter control sequence used during the growth is described elsewhere.6 Two types of samples were studied. One was single ␦-doped (sam- ple A), where only a small enhancement in the net- acceptor concentration was obtained; the other was ␦3 -doped (sample B), and a significant increase of the net-acceptor concentration was obtained. PHOTOLUMINESCENCE RESULTS In Figs. 1 and 2, we show the PL from samples A and B (both have Te content of ϳ0.5%). The PL from both samples shifts to red with decreasing excitation Journal of ELECTRONIC MATERIALS, Vol. 31, No. 7, 2002 Special Issue Paper Heavily p-Type Doped ZnSe Using Te and N Codoping Y. GU,1,3 IGOR L. KUSKOVSKY,1 G.F. NEUMARK,1 W. LIN,2 S.P. GUO,2 O. MAKSIMOV,2 and M.C. TAMARGO2 1.—Department of Applied Physics and Applied Mathematics, Columbia University, New York, NY 10027. 2.—Chemistry Department, City College of CUNY, New York, NY 10007. 3.—E-mail: yg99@columbia.edu We have studied photoluminescence (PL) of ZnSe samples codoped with Te and N in ␦-layers. We have concluded that Te clusters are involved in the PL. We also compared the PL data of samples with lower Te concentrations to those with higher Te concentrations; the results corroborate the Te-cluster conclu- sion. Key words: ZnSe, Te clusters, photoluminescence, p-type (Received October 3, 2001; accepted March 2, 2002) 799
  • 2. intensity, with such a shift being considered a hall- mark of a donor-acceptor pair (DAP) PL.8 The PL of sample A shows a series of peaks at 2.686 eV, 2.655 eV, 2.625 eV, and 2.594 eV. These peaks are sepa- rated by 30–31 meV, which is about the ZnSe longi- tudinal-optical phonon energy.9 However, it is clear from Fig. 1 that the intensity of the peak at 2.655 eV does not scale with the intensity of the 2.686-eV peak, which indicates that these two peaks are asso- ciated, at least partly, with different centers. Also, we note that the peak at 2.655 eV is in the 2.63–2.68-eV energy range, where we have previously observed PL caused by excitons bound to Te pairs and/or clusters.10 Therefore, we suggest that this 2.655-eV peak has some contributions from the recombination of exci- tons bound to such Te complexes. As to the 2.686-eV peak, it is very close to the peak position of the “deep” DAP emission in ZnSe:N.11 The current value is slightly high, but the present system is expected to have a relatively strong Coulomb shift because of preferential DAP11 emission, which could account for this. Furthermore, it can be seen that, at low-excita- tion intensity, this sample shows a small broad shoulder at around 2.42 eV (Fig. 3), which is in the range of the peak position (2.487 eV) of excitons bound to TenՆ3 clusters.10 Therefore, even though the Te concentration is as low as 0.5% in this sample, it still shows quite efficient Te-cluster-related PL. This can be understood by considering the geometry of our sample, which could result in relatively high Te concentration in the ␦-doped layer. As to sample B, it shows only one broad peak at around 2.457 eV. As mentioned, this peak shifts to red with decreasing excitation intensity. However, 2.457 eV is too deep for the “ordinary” DAP peaks in ZnSe. Furthermore, as mentioned previously, this peak is close to the one assigned to excitons bound to TenՆ3 clusters. Therefore, we believe that, in addition to N, Te clusters are also involved in this transition. Previously, we reported PL spectra of another set of ␦- and ␦3 -doped ZnSe:(N ϩ Te) samples12 with 800 Gu, Kuskovsky, Neumark, Lin, Guo, Maksimov, and Tamargo Table I. The Net Acceptor Concentrations Te Samples and Spacer NA Ϫ ND Concentration Doping (ML) (cm Ϫ3 ) (%) Uniform ZnSe:N N/A 3.0 ϫ 1017 N/A ␦-ZnSe:(N) N/A 5.6 ϫ 1017 N/A ␦-ZnSe:(Te, N) 10 1.5 ϫ 1017 ϳ0.5 ␦3 -ZnSe:(Te, N) 12 4.0 ϫ 1017 Ͻ3 ␦3 -ZnSe:(Te, N) 7 6.0 ϫ 1017 Ͻ1.8 Fig. 1. PL spectra of sample A at different excitation intensities at T ϭ 10K. Fig. 2. PL spectra of sample B at different excitation intensities at T ϭ 10K. Fig. 3. The PL spectra of sample A at low-excitation intensity.
  • 3. higher Te concentrations (1.8% and 3%, respec- tively). It is instructive to compare those results with those of our new samples with less Te concen- trations (0.5%). In Fig. 4, we plot the integrated in- tensity versus the excitation intensity for each of our new samples, which show one slope for sample A (␦-doped) and two slopes for sample B (␦3 -doped). We note that with our previous samples, there are two distinct slopes for each of them. Because the only difference between the new ␦-doped sample and the previous one is the Te concentration, the difference in slopes corroborates our conclusion that Te is in- volved in the PL. Regarding the two-slope case, as discussed in Refs. 12 and 13, the plots show two slopes if two recombination paths are present. We, thus, note that despite the low Te content of the new sample, the ␦3 geometry still gives a large number of Te complexes around the ␦3 -layer region, enough to give two paths. We also note that the PL-peak posi- tion of the new ␦3 -doped sample is higher than that of the previous one. This could be due to the fact that the previous ␦3 -doped sample has more TenՆ3 clus- ters, or alternatively, a sufficiently high Te concen- tration to change the bandgap for this effect to take place. SUMMARY In summary, we employed a modulation-doping technique that allowed us to achieve a net-acceptor concentration as high as 6 ϫ 1018 cmϪ3 with Te less than 1.8%. The low-temperature PL spectra of these samples showed dominant Te-related peaks but also involved N. We also compared the PL spectra of our present samples (with lower Te concentrations) to that of previous samples (with higher Te concentra- tions). The results are consistent with our conclu- sion that Te clusters are involved in the PL. ACKNOWLEDGEMENT The authors acknowledge the support of the De- partment of Energy under Grant Nos. DE-FG02- 98ER45694 and DE-FG02-98ER45695. REFERENCES 1. R. Haitz, F. Kish, J. Tsao, and J. Nelson, Comp. Semicond. 6, 34 (2000). 2. A. Weinert, Plastic Optical Fibers: Principles, Components, Installation (Erlangen and Munich: Publicis MCD Verlag, 1999). 3. G.F. Neumark, Mater. Lett. 30, 131 (1997). 4. H.D. Jung, C.D. Song, S.Q. Wang, K. Arai, Y.H. Wu, Z. Zhu, T. Yao, and H. Katayama-Yoshida, Appl. Phys. Lett. 70, 1143 (1997). 5. W. Faschinger, J. Nurnberger, E. Kurtz, R. Schmitt, M. Korn, K. Schull, and M. Ehinger, Semicond. Sci. Technol. 12, 1291 (1997). 6. W. Lin, S.P. Guo, M.C. Tamargo, I.L. Kuskovsky, C. Tian, and G.F. Neumark, Appl. Phys. Lett. 76, 2205 (2000). 7. I.L. Kuskovsky, Y. Gu, C. Tian, G.F. Neumark, S.P. Guo, W. Lin, O. Maksimov, M.C. Tamargo, A.N. Alyoshin, and V.M. Belous, Phys. Status Solidi (b) 229, 385 (2002). 8. J.I. Pankove, Optical Process in Semiconductor (New York: Dover, 1974). 9. H. Hartman, R. Mach, and B. Selle, “Wide Gap II–VI Com- pounds as Electronic Materials,” Current Topics in Materi- als Science, vol. 9, ed. E. Kaldis (Amsterdam: North-Hol- land, 1982). 10. I.L. Kuskovsky, C. Tian, G.F. Neumark, J.E. Spanier, I.P. Herman, W. Lin, S.P. Guo, and M.C. Tamargo, Phys. Rev. B 63, 155205 (2001). 11. G.F. Neumark, L. Radomsky, and I. Kuskovsky, Proc. SPIE 2346, 159 (1994). 12. I.L. Kuskovsky, C. Tian, C. Sudbrack, G.F. Neumark, W.-C. Lin, S.P. Guo, and M.C. Tamargo, J. Appl. Phys. 90, 2269 (2001). 13. V.V. Serdyuk, G.G. Chemeresyuk, and M. Terek, Photoelec- trical Processes in Semiconductors (Kiev-Odessa: Vischa Shkola, 1982) (in Russian). Heavily p-Type Doped ZnSe Using Te and N Codoping 801 Fig. 4. The integrated PL intensity as a function of laser-excitation intensity: (a) ␦-doped ZnSe:Te, N) and (b) ␦3 -doped ZnSe:(Te, N).
  • 4. COPYRIGHT INFORMATION TITLE: Heavily p-Type Doped ZnSe Using Te and N Codoping SOURCE: J Electron Materns Part A 31 no722 Jl 20021998 The magazine publisher is the copyright holder of this article and it is reproduced with permission. Further reproduction of this article in violation of the copyright is prohibited. To contact the publisher: http://www.springerlink.com/content/0361-5235/