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Optimization of annealing of dopant to increase sharpness of p–n junctions in a heterostructure with drain of dopant

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Abstract

It has been recently shown, that manufacturing of p–n junctions by dopant diffusion or ion implantation in heterostructures and optimization of annealing time leads to increasing of their sharpness and homogeneity of dopant distribution in enriched area. In this paper, we consider influence of defects of doped structure (mismatch dislocations and similar), which became as drain of atoms of dopant, on dopant distribution in diffusive-junction rectifier.
ORIGINAL ARTICLE
Optimization of annealing of dopant to increase sharpness
of pn junctions in a heterostructure with drain of dopant
E. L. Pankratov
E. A. Bulaeva
Received: 25 March 2013 / Accepted: 25 April 2013
Ó The Author(s) 2013. This article is published with open access at Springerlink.com
Abstract It has been recently shown, that manufacturing of
pn junctions by dopant diffusion or ion implantation in
heterostructures and optimization of annealing time leads to
increasing of their sharpness and homogeneity of dopant
distribution in enriched area. In this paper, we consider
influence of defects of doped structure (mismatch disloca-
tions and similar), which became as drain of atoms of dopant,
on dopant distribution in diffusive-junction rectifier.
Keywords Diffusion-heterojunction rectifier Modeling
of dopant diffusion Accounting drain of dopant
Optimization of annealing of dopant
Introduction
In the present time, elaboration of new devices of solid
state electronic devices is intensively done. The second
way for intensive elaboration is refinement of characteris-
tics of traditional solid state electronic devices (Esmaeili-
Rad et al. 2007; Huang et al. 2003; Lai et al. 2007; Kitada
et al. 2009; Lei et al. 2009; Volocobinskaya et al. 2001;
Vasil’ev et al. 2002). One of the questions of the refine-
ment is increasing of sharpness of pn junctions and
manufacturing the devices as more shallow (Andronov
et al. 1998; Sisiyany et al. 2002). One way to increase
sharpness of pn junction is using laser annealing (Va-
ronina et al. 1999; Pankratov 2005). The second one is
using inhomogeneity of heterostructure (H) (Kelleher et al.
2009; Pankratov 2010, 2012). It could be used as another
standard of approach. In this paper, we consider an
approach to increase sharpness of diffusive-junction recti-
fier using defects of doped structure.
In this paper, we consider a H with two layers (see
Fig. 1). One layer is a substrate (S). The second one is an
epitaxial layer (EL). A dopant has been infused in the EL.
One can obtain increasing of sharpness of the diffusive-
junction rectifier and at the same time increasing of
homogeneity of dopant distribution in the rectifier after
that, when dopant achieves the interface between layers of
H (see Fig. 2). Recently it has been shown, that after
annealing of dopant with optimal value of annealing time
H compromise between increasing of sharpness of p
n junction and increasing of homogeneity of dopant dis-
tribution in the rectifier could be achieved (Pankratov 2005,
2010, 2012). Main aim of the present paper is taking into
account drains of atoms of dopant on defects of doped
structure (mismatch dislocations and similar).
Method of solution
Redistribution of dopant has been described by the second
Fick’s law (Shalimova 1985;Gotra
1991;Alexandrov2002)
oCx; tðÞ
ot
¼
o
ox
D
C
oCx; tðÞ
ox

k
R
x; TðÞCx; tðÞ
þ k
G
x; TðÞCx; tðÞ: ð1Þ
Here C(x,t) is the spatiotemporal distribution of dopant;
D
C
is the dopant diffusion coefficient; k
R
(x,T) is the
E. L. Pankratov (&)
Nizhny Novgorod State University, 23 Gagarin avenue,
Nizhny Novgorod 603950, Russia
e-mail: elp2004@mail.ru
E. A. Bulaeva
Nizhny Novgorod State University of Architecture and Civil
Engineering, 65 Il’insky street, Nizhny Novgorod 603950,
Russia
e-mail: hellen-bulaeva@yandex.ru
123
Appl Nanosci
DOI 10.1007/s13204-013-0228-7
parameter, which characterize speed of capturing of atoms
of dopant by drains; k
G
(x,T) is the parameter, which
characterize speed of returning of atoms of dopant from
drains. We transform the Eq. (1) to the following form by
combination of two last terms into one
oCx; tðÞ
ot
¼
o
ox
D
C
oCx; tðÞ
ox

Kx; TðÞCx; tðÞ; ð1aÞ
where K(x,T) = k
R
(x,T) - k
G
(x,T). The Eq. (1)is
complemented by the following boundary and initial
conditions
oCx; tðÞ
ox
x¼0
¼
oCx; tðÞ
ox
x¼L
¼ 0; Cx; 0ðÞ¼f
C
xðÞ: ð2Þ
The conditions have been written in the most common
form. However dopant usually did not achieves the
boundary x = L of H. In this situation, appropriate
boundary condition could be written as: C(L,t) = 0.
Value of diffusion coefficient D
C
depends on properties of
materials of H, velocities of heating and cooling (with account
Arrhenius law) of the materials and spatiotemporal distribu-
tion of dopant concentration. The last dependence could be
approximated by the following function (Gotra 1991)
D
C
¼ D
L
x; TðÞ1 þ n
C
c
x; tðÞ
P
c
x; TðÞ

: ð3Þ
Here D
L
(x,T) is spatial (due to inhomogeneity of H) and
temperature (due to Arrhenius law, where T is the
temperature) dependences of diffusion coefficient;
P(x,T) is the limit of solubility of dopant; parameter c
depends on properties of materials and could be integer in
the interval c [ [1,3] (Gotra 1991). Concentrational
dependence of diffusion coefficient is discussed in detail
in (Gotra 1991).
To determine spatiotemporal distribution of dopant
concentration let us use the method of averaging of func-
tion correction (Pankratov 2010; Alexandrov 2002). To use
the approach we transform the Eq. (1a) to the following
integral form
Cx; tðÞ¼Cx; tðÞþ
1
L
2
Z
t
0
D
L
x; TðÞ1 þ n
C
c
x; sðÞ
P
c
x; TðÞ

8
<
:
Cx; sðÞds
Z
t
0
Z
x
0
Kv; TðÞCv; sðÞx vðÞdvds
Z
t
0
Z
x
0
Cv; sðÞ1 þn
C
c
v; sðÞ
P
c
v; TðÞ

oD
L
v; TðÞ
ov
dvds
þ
Z
t
0
Z
L
0
Cx; sðÞ1 þn
C
c
x; sðÞ
P
c
x; TðÞ

oD
L
x; TðÞ
ox
dxds
þ
Z
t
0
Z
L
0
L xðÞKx; TðÞCx; sðÞdxds þ
Z
L
0
L xðÞCx; tðÞdx
Z
x
0
x vðÞCv; tðÞdv
Z
L
0
L xðÞfxðÞdx þ
Z
x
0
x vðÞfvðÞdv
9
=
;
:
ð1bÞ
To determine the first-order approximation C
1
(x,t)of
dopant concentration let us replace determining function
C(x,t) in the right side of Eq. (1b) on its average value a
1
.
After the replacement one can obtain the following relation
for the first-order approximation C
1
(x,t) of dopant
concentration in the following form
D(x),
P
(x)
C(x,0)
D
EL
P
EL
D
S
P
S
L
a
0
Substrate
Epitaxial layer
Fig. 1 Heterostructue with epitaxial layer and substrate
x
C
(
x
,
Θ
)
L
/4
L
/2
03
L
/4
L
1
2
3
4
Fig. 2 Dopant distributions for different values of annealing time.
Increasing of number of curves corresponds to increasing of value of
annealing time. Interface between layers coincides with midpoint of
the heterostructure, i.e., x = L/2
Appl Nanosci
123
C
1
x; tðÞ¼a
1
þ
1
L
2
a
1
Z
t
0
D
L
x; TðÞ1 þ
na
c
1
P
c
x; TðÞ

ds
8
<
:
a
1
Z
t
0
Z
x
0
x v
ðÞ
Kv; T
ðÞ
dvds a
1
Z
t
0
Z
x
0
1 þ
na
c
1
P
c
v; TðÞ

oD
L
v; TðÞ
ov
dvds
þ a
1
Z
t
0
Z
L
0
L xðÞKx; TðÞdxds þ
Z
t
0
Z
L
0
oD
L
x; TðÞ
ox
a
1
1 þ
na
c
1
P
c
x; TðÞ

dxds þ
a
1
2
L
2
x
2

Z
L
0
L xðÞfxðÞdx þ
Z
x
0
x vðÞfvðÞdv
9
=
;
The average value a
1
of the function C
1
(x,t) could be
determined by the following standard relation
a
i
¼
1
LH
Z
H
0
Z
L
0
C
i
x; tðÞdxdt; ð4Þ
where H is the observation time on diffusion process.
Integration of the function C
1
(x,t) with account relation (4)
leads to the following equation for the average value a
1
,
which depends on parameter c
a
1
Z
H
0
H tðÞ
Z
L
0
D
L
x; TðÞ1 þ
na
c
1
P
c
x; TðÞ

dxdt
a
1
2
Z
H
0
H tðÞ
Z
L
0
L
2
x
2

Kx; TðÞdxdt
a
1
Z
H
0
H tðÞ
Z
L
0
L xðÞ1 þ
na
c
1
P
c
x; TðÞ

oD
L
x; TðÞ
ox
dxdt
þ a
1
Z
H
0
Z
L
0
L xðÞKx; TðÞdx H tðÞds
þ a
1
Z
H
0
H tðÞ
Z
L
0
1 þ
na
c
1
P
c
x; TðÞ

oD
L
x; TðÞ
ox
dxds
þ
Z
L
0
L
2
x
2

fxðÞdx
H
2
þ L
3
H
a
1
3
HL
Z
L
0
L xðÞfxðÞdx ¼ 0:
The second-order approximation of dopant
concentration C
2
(x,t) could be determined by standard
iteration procedure of method of averaging of function
correction (Pankratov 2010; Sokolov 1955), i.e., by
replacement the determining function C(x,t) in the right
side of the Eq. (1b) on sum of average value a
2
of the
second-order approximation of dopant concentration
C
2
(x,t) and the first-order approximation of dopant
concentration C
1
(x, t). In this case, the second-order
approximation could be written as
C
2
x; tðÞ¼a
2
þ C
1
x; tðÞþ
1
L
2
Z
t
0
D
L
x; TðÞ
0
@
a
2
þ C
1
x; sðÞ½1 þ n
a
2
þ C
1
x; sðÞ½
c
P
c
x; TðÞ

ds
Z
t
0
Z
x
0
x vÞ
ð
Kv; T
ðÞ
a
2
þ C
1
v; s
ðÞ½
dvds
þ
Z
t
0
Z
L
0
Kx; TðÞL xðÞa
2
þ C
1
x; sðÞ½dxds
þ
Z
t
0
Z
L
0
C
1
x; sðÞ½þa
2
1 þ n
a
2
þ C
1
x; sðÞ½
c
P
c
x; TðÞ

oD
L
x; TðÞ
ox
dxds
Z
t
0
Z
x
0
oD
L
v; TðÞ
ov
1 þ n
a
2
þ C
1
v; sðÞ½
c
P
c
v; TðÞ

a
2
þ C
1
v; sðÞ½dvds
Z
L
0
L xðÞfxðÞdx þ
Z
L
0
L xðÞa
2
þ C
1
x; tðÞ½dx
Z
x
0
x vðÞa
2
þ C
1
v; tðÞ½dv þ
Z
x
0
x vðÞfvðÞdv
1
A
:
Average value a
2
of the second-order approximation of
dopant concentration could be determined by the standard
relation (4). After substitution of the function C
2
(x,t) in the
relation (4), we obtain the equation for the average value a
2
in the following form
Z
H
0
H tðÞ
Z
L
0
D
L
x; TðÞa
2
þ C
1
x; tðÞ½1 þn
a
2
þ C
1
x; tðÞ½
c
P
c
x; TðÞ

dxdt
1
2
Z
H
0
H tðÞ
Z
L
0
Kx; TðÞL
2
x
2

a
2
þ C
1
x; tðÞ½dxdt
þ L
Z
H
0
Z
L
0
a
2
þ C
1
x; tðÞ½1 þ n
a
2
þ C
1
x; tðÞ½
c
P
c
x; TðÞ

oD
L
x; TðÞ
ox
dx
H tðÞdt þ LH
Z
H
0
Z
L
0
L xðÞa
2
þ C
1
x; tðÞ½dxdt
Appl Nanosci
123
L
Z
H
0
H tðÞ
Z
L
0
L xðÞ1 þn
a
2
þ C
1
v; tðÞ½
c
P
c
v; TðÞ

a
2
þ C
1
v; tðÞ½
oD
L
v; TðÞ
ov
dvdt þ L
Z
H
0
H tðÞ
Z
L
0
L xðÞ
a
2
þ C
1
x; tðÞ½Kx; TðÞdxdt þ
H
2
Z
L
0x
fxðÞL
2
x
2

dx
HL
Z
L
0
L xðÞfxðÞdx
1
2
Z
H
0
Z
L
0
L xðÞa
2
þ C
1
x; tðÞ½dxdt ¼ 0:
Analysis of spatiotemporal distribution of dopant
concentration has been done analytically using the second-
order approximation framework method of averaging of
function correction and has been amended numerically.
Discussion
In this section, we analyzed influence of drains of atoms of
dopant on distribution of their concentration in diffusion-
junction rectifier. Some distributions of dopant, which
corresponds to the rectifier, are present in Fig. 3. In this
case drain of the atoms is presented on the right side of the
heterostructure. Increasing of number of curve corresponds
to increasing of value of annealing time. The figure shows,
that availability of drain leads to decreasing of sharpness of
the rectifier. Analogous conclusion could be done in the
case, when drain of atoms of dopant is presented on the
interface between layers of H. The decreasing of sharpness
could be though partially compensated using inhomoge-
neity of heterostructure and nonlinearity of diffusion pro-
cess. The nonlinearity leads to large influence, when level
of doping of materials is high (Pankratov 2005).
Conclusion
In this paper, we analyzed influence of drain of atoms of
dopant on distribution of their concentration in diffusion-
junction rectifier. It has been shown, that availability of
drain leads to decreasing sharpness of pn junction. It has
been considered abilities of compensation of the
decreasing.
Acknowledgments This work is supported by the contract
11.G34.31.0066 of the Russian Federation Government and educa-
tional fellowship of President of Russia.
Open Access This article is distributed under the terms of the
Creative Commons Attribution License which permits any use, dis-
tribution, and reproduction in any medium, provided the original
author(s) and the source are credited.
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It has recently been shown that the interface between layers of a heterostructure makes it possible to increase the sharpness of the p-n junction and the homogeneity of an impurity distribution in doped areas, and also to control the depth of the junction. In this work the dynamics of a dopant concentration in an inhomogeneous semiconductor structure has been analyzed, taking into account the temporal and concentrational dependence of the diffusion coefficient. The optimization of the parameters and the annealing time for production of the p-n junction with smaller parasitic capacitance has been done. It has been shown that doubling the annealing time in comparison with its optimal value leads to variation of the sharpness of the p-n junction from 10% to 200%.
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We have studied the behavior of various intrinsic emission zones on the characteristics of organic light-emitting diodes with a p-doped hole-transport layer and an n-doped electron-transport layer based on our previous work [J. S. Huang, M. Pfeiffer, A. Werner, J. Blochwitz, K. Leo, and S. Liu, Appl. Phys. Lett. 80, 139 (2002)]. This configuration is referred to as a PiN structure. Because the p- and n-doped regions occupy nearly 80% of the total thickness in our PiN device, the intrinsic region becomes a narrow layer between two doped regions. This intrinsic region includes the region where the radiative recombination occurs. Thus, the nature of this layer plays an important role in determining the actual device performance. Employing 8-tris-hydroxyquinoline aluminum as an emitter, we investigated the influence of the thickness of the emitter layer on the performance of the device. The optimum thickness of the emitter layer is found to be 20 nm. Combining the fluorescence dye doping method, we have optimized the PiN structure device. Two emitter systems have been used: Alq3 doped with two highly fluorescent laser dyes, Quinacridone or Coumarin 6, respectively. We have demonstrated the influence of the thickness and the doping of the emission zone on the characteristics of a doped emitter device with PiN structure, and obtained higher-efficiency PiN structure devices. The different properties of PiN devices corresponding to two different emitter dopants with different trapping effect are also discussed. © 2003 American Institute of Physics.
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We demonstrate that mode-locking of ytterbium fiber lasers with a carbon nanotube saturable absorber can produce pulses ranging from 20 ps to 2 ns at repetition rates between 21 MHz and 177 kHz, respectively, depending on cavity length. Nonlinear polarization evolution is not responsible for mode-locking. Even in the nanosecond regime, clean single pulses are observed and the pulse train exhibits low jitter. Combined with extremely large chirp, these properties are suited for chirped-pulse amplification systems.
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The study of the photosensitivity of an In-SiO2-Cd0.28Hg0.72Te metal-insulator-semiconductor structure with an opaque electrode is continued and the results are reported in this paper. The effect of a drastic decrease in photosensitivity with increasing inversion voltage is considered. This effect manifests itself both under unmodulated illumination (measurements of photocapacitance) and under modulated illumination (measurements of photovoltage), with the onset of a decrease in photovoltage coming ahead of that in photocapacitance. It is believed that this effect is caused by an increase in the longitudinal resistance of the inversion layer and by the anomalous generation of charge carriers at the semiconductor-insulator interface; as a result of the latter, the resistance of the induced p-n junction decreases.