06jno02 1149
06jno02 1149
06jno02 1149
In this work we investigated propagation of ultrashort laser pulses in Tellurite glass codoped
Er3+ /Tm3+ . We derived a general propagation equation of pulses which includes the linear and non-
linear effects to all orders. We studied in the specific case of Kerr media and obtained an ultrashort
pulse propagation equation called a generalized nonlinear Schrödinger equation. The impact of
the third order dispersion, the higher-order nonlinear terms self-steepening, and stimulated Raman
scattering are explicitly analyzed.
Keywords: Femtosecond Pulse Propagation, Kerr Medium, Group Velocity Dispersion, Third
Order Dispersion, Self Steepening, Raman Scattering.
RESEARCH ARTICLE
and it exhibits better environmental resistance than fluo-
process of ultrashort laser pulses (in fs) in a medium have ride fibers, in addition, Tellurite glass provides a much
been the subject of intensive research within the last few broader fluorescence spectra and larger rare earth oxide
years.1 2 6 7 Because of special properties of these pulses, solubility than silicate and fluoride glasses.8–9 Recently,
during their propagation in the medium several new effects Tm3+ -doped Tellurite fiber for S-band amplification were
have been observed in comparison with the propagation reported under dual-wavelength pumping (795/1064 nm
process of short pulses (in ps), namely the effects of dis- and 1047/1550 nm) schemes.10 11
persion and nonlinear effects of higher orders. Under the
The Tellurite glass presents very good optical quality, is
influence of these effects, we have complicated changes
stable against atmospheric moisture, it exhibits low opti-
both in amplitude and spectrum of the pulse. It splits
cal attenuation from 400 nm to 5.0 m, The material
into constituents and its spectrum also evolves into sev-
also exhibits high solubility allowing the incorporation
eral bands which are known as optical shock and self-
of high lanthanide concentrations apart from being non
frequency shift phenomena.1–3 5
hygroscopic and to present high thermal stability against
These effects should be studied in detail for future con-
crystallization.12
crete applications of femtosecond pulses, especially in
In recent years, the upconversion of infrared light to vis-
the domain of optical communication. We apply the gen-
ible light by rare earth ion doped glasses has been investi-
eral formalism used for the pulse propagation problem in
gated extensively, due to the possibility of infrared pumped
Ref. [4] for the one-dimensional case.31
visible lasers and the potential applications in areas such as
This formalism is based on the approximate expansion
three-dimensional display, optical data storage, optoelec-
of the nonlinear wave equation, which treats the nonlinear
tronics, medical diagnostics, sensor, and undersea optical
processes involved in the problem as the perturbations.
communication.13–17
2. TELLURITE GLASS
2.2. Spectroscopy Properties
2.1. Definitions
Absorption spectra of Er3+ -doped and Er3+ /Tm3+ -codoped
Tellurite glass fibers exhibit significant advantages over Tellurite glasses and their correspondent energy levels are
the fluoride and silicate glass fibers for amplification presented in Figure 2.
Wavelength
Fig. 1. The absorption spectrum of Tm3+ /Er3+ /Yb3+ -codoped TPCFB
glass.13–17 Fig. 3. Curves of the refractive index according to the wavelength in
the visible field.
2.3. Refractive Index
glasses. All curves show about 0.5 cm−1 minimum attenua-
The refraction index of these glasses is relatively high and
tion for wavelength above 800 nm, but, with the exception
depends on the wavelength () according to18
of the first curve, (a), they were vertically displaced arbi-
trarily to display more clearly the Tm3+ ions absorption
3242
n ≈ 1 + 2 (1) bands.18
− 1932
β2 = 0.0792 ps2/m
at 800 nm
β3 = –1.02.10–5 ps3//m
at 800 nm
Wavelength
Fig. 2. Energy levels for Er3+ and Tm3+ -doped Tellurite glass. On the
right, the spectrum of energy of Tm3+ (078 · 1020 ions/cm3 -doped Tel- Fig. 4. Variation of 2 and 3 with wavelength for Tellurite glass
lurite glass is presented.18 Codoped Er3+ /Tm3+ .
RESEARCH ARTICLE
general, the spectrum consists of many peaks, and the out-
We confine our self only to consider the propagation of
ermost peaks are the most intense. The number of peaks
the electric field in an arbitrary direction, say Oz (usually,
depends on ∅max and increases linearly with it. The origin
chosen as the direction of k 0 ), so we can write
of the oscillatory structure can be understood by refer-
1 ring to Ref. [19], where the time dependence of the SPM-
t = xEz
Er t = x Az te−iw0 t+ik0 z + C · C (3)
2 induced frequency chirp is shown.
Figure 7 compares the pulse spectra for Gaussian
The nonlinear Schrodinger equation that governs prop- (m = 1 and super-Gaussian (m = 3 pulses obtained. In
agation of optical pulses inside single fiber is given by
A A i2 2 A
+ 1 + + A = i A 2 A (4)
z t 2 t2 2
where the nonlinear parameter is defined as
n 2 w0 3
= · n2 = 3
Rexxxx (5)
cAeff 8n
The parameter Aeff is known as the effective core area
and is defined as
+
− F x y2 dxdy2
Aeff = + (6)
−
F x y4 dxdy
Fig. 7. SPM-broadened spectra for an unchirped Gaussian pulse. Spec- The appropriate propagation equation for the amplitude
tra are labeled by the maximum nonlinear phase shift ∅max . (in the left Az T is obtained from Eq. (9) after setting = 0.
for Gaussian pulse m = 0, and right for super-Gaussian pulse m = 3), U z T satisfies the following equation:
0 = 100 fs, LNL = 714 m.
U 2U 3U
i = 2 2
+i 3 (11)
both cases, input pulses are assumed to be unchirped z 2 T 6 T3
(C = 0. The fiber length and the peak power are chosen Figure 8 shows the pulse shapes at z = 200LD for an
such that ∅max = 50. (Comparison with silica fiber see initially unchirped Gaussian pulse (C = 0) for 3 = 0 (dot-
after Agrawal19 ∅max = 45, 0 = 1 ps). ted curve) and for a value of 2 = 792e − 5 ps2 /m and
3 = −102e − 8 ps3 /m (dashed curve). Whereas a Gaus-
sian pulse remains Gaussian when only the 2 term in
4. IMPACT OF DISPERSION AND Eq. (11) contributes to GVD, the TOD do not distorts the
HIGHER-ORDERNONLINEAR EFFECTS pulse because have negligible values. Comparison with sil-
RESEARCH ARTICLE
ON THE ULTRASHORT PULSES ica fiber see after Agrawal19 z = 5LD 0 = 1 ps).
Under the influence of TOD both the pulse shape and
For pulses shorter than 5 ps but wide enough to contain
spectrum change in a complicated way. When the prop-
many optical cycles (widths 10 fs), we can obtain:
agation distance is larger the oscillation of the envelope
A i 2 A 3 A function is stronger, creating a long trailing edge to the
+ A+ 2 2 − 3 3 later time, and the spectrum is broadened into two sides
z 2 2 t 6 t
and splits to the several peaks.24 26
i A 2
= i A 2 A + A 2 A − TR A (9)
w0 T T
RESEARCH ARTICLE
value of s, the two solitons have separated from each other and for the long distance of the propagation, this effects
within a distance of two soliton periods and continue to change the form of the pulse relatively.31 Figure 10 shows
move apart with further propagation inside the Tellurite such a decay for a second-order soliton (N = 2 by solving
glass. (Comparison with silica fiber see after Agrawal,19 Eq. (13) numerically with R = 001. (Comparison with
z = 5/2, s = 02, 0 = 1 ps). silica fiber see after Agrawal19 z = 5/2, and 0 = 1 ps).
A qualitatively similar behavior occurs for smaller values
of s except that a longer distance is required for the breakup
4.4. Generalized Nonlinear Schrodinger Equation
of solitons. In the absence of self-steepening (s = 0, the
two solitons form a bound state because both of them prop- For the ultrashort pulses with the width 0 = 100 fs
agate at the same speed (the eigenvalues have the same real and the carrier wavelength 0 = 08 m the higher-order
Fig. 9. Decay of a second-order soliton N = 2 induced by self- Fig. 10. Decay of a second-order soliton (N = 2 induced by intrapulse
steepening s = 00042, 0 = 100 fs, z = 10/2. Raman scattering R = 001 0 = 100 fs, z = 50/2.