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Time-dependent theoretical model for terahertz wave detector using a parametric process

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Abstract

We have presented a time-dependent theoretical model to describe the time behavior of a quasi-monochromatic nanosecond terahertz detector reported by Guo et. al. (2008 Appl. Phys. Lett. 93, 021106). The temporal input-output characteristic of the detector is investigated numerically by taking the system parameters close to the experimental ones, and the calculated pulse width for the incident terahertz wave agrees well with the experimental one. Our results demonstrate that the energy and width of an output idler wave pulse are proportional to those of the incident terahertz wave pulse. This study provides a strict theoretical basis and could be used to guide the design and optimization for the highly sensitive coherent terahertz detector.

© 2010 Optical Society of America

1. Introduction

Over the past decades the generation and detection of terahertz (THz) pulses have progressed rapidly since these pulses allow many fascinating and important applications, such as medical diagnosis [1,2], and security inspection [3]. Several methods have been developed for the detection of THz pulses, all of which have their specific merits. For instance, it has been demonstrated that a Si bolometer is a very sensitive detector. However, a severe disadvantage of the bolometer is that it must be operated at cryogenic temperatures to reduce noises. Moreover, the bolometer is a square-law detector, which loses all information about the phase of a THz electric field. Thus, there is a critical need for a sensitive detector that works at non-cryogenic temperature. Recently, Guo and the co-operators reported an experiment for coherent detection of narrow-linewidth nanosecond THz radiation at room temperature using a parametric process in nonlinear MgO:LiNbO3 crystals, which demonstrated a new way to realize a kind of THz wave detector that was capable of capturing the temporal profile of THz pulses with nanosecond resolution [4]. Such a detector has several advantages: First, it has at least the sensitivity of an order or more than a typical Si bolometer does for detecting nanosecond THz wave pulses. Second, it could operate at room temperature, unlike a liquid-He-cooled Si bolometer that must work at 4.2 K to reduce noise. And last but not least, room-temperature direct THz wave detectors such as pyroelectrics and Golay cells offer poor sensitivity.

The main optical part of such a detector consisted of two pieces of MgO:LiNbO3 crystals, as shown in Fig. 1(a). In the first crystal, an intense near-infrared pump beam (ω p) was normally incident on and totally reflected at the inner probe surface of the crystal. The reflected pump light interacted with an incident THz wave (ω T), thus generating a light wave (namely idler wave) at a difference frequency (ω id = ω pω T) due to stimulated polariton scattering [5,6]. Nearly all of the THz wave are absorbed due to the heavy absorption loss or are totally reflected by the right beveled side of the first crystal due to the large refractive index (greater than 5) in THz range [7,8].The pump light and the idler light were then incident to the second crystal, in which the idler light was parametrically amplified. The output idler light was detected with an InGaAs-based photodiode. It was believed that the intensity of the output idler light should be proportional to the intensity of the incident THz wave, which was confirmed by the experiment. The parameters of the incident THz wave could then be determined by studying the measured idler light. Obviously, it needs a strict theoretical model to describe the characteristic of the detector and to guide the design of the detector in the further. Very recently, we established a steady-state model for the detector [9], which can explain the main experimental results and can provide some proposals to improve and optimize the detector to some extent. However, because the detector is operated at unsteady state, the steady-state model does not work well all the time. Therefore, in this paper we establish a time-dependent theoretical model to describe the temporal behavior of the detector. Our results demonstrate that the pulse width and energy of the output idler wave are proportional to those of the incident THz wave for the case of no pump depletion. Such a linear relationship indicates that the system consisted of two pieces of LiNbO3 (LN) crystals can be used as a detector to measure a nanosecond THz wave pulse. Some proposals to improve and optimize the detector are provided.

2. Theoretical analyses

 figure: Fig. 1.

Fig. 1. Schematic diagrams (a) the THz wave detector made of two LN crystals reported in [4], and (b) wave configuration, boundary conditions and coordinate system.

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In our analysis, the wave pulses propagate in the x-z plane with their direction of polarization along y-axis (paralleling to the c-axis of the crystal), as shown in Fig. 1(b). For the case that the effects of higher-order dispersion [10,11] and transverse diffraction are ignored and for quasi-monochromatic pulses, from Maxwell equations we can derive the coupled equation as

(z+1ut)A(z,t)=iω022k0zε0c2pNL(z,t)exp[i(k0zz+φ0)],

where ε 0 is the vacuum permittivity, c is the light velocity in the vacuum, A(z,t) and p NL(z,t) are the slowly varying field envelope and the nonlinear polarization, respectively, ω 0 is the angular frequency, k0z is the z-component of wave vector at ω 0, φ 0 is the initial phase. More details of the derivation processes can be found in Appendix.

For the case that the frequency of the THz wave is lower than or close to the phonon vibration frequency of the crystal, while the frequencies of the pump and idler waves are much higher than the phonon vibration frequency, following some pioneers’ works [12–14], the coupled wave equations can be written as

(z+1upt)Ap(z,t)=iω0p2n0pc{χp(3)(ω0p;ω0pω0id,ω0id)Aid(z,t)2Ap(z,t)
+χp(2)(ω0p;ω0id,ω0T)Aid(z,t)AT(z,t)exp[i(Δk0zz+Δφ)]},
(z+1uTt)AT(z,t)=iω0T2n0Tc{χT(1)(ω0T)AT(z,t)
+χT(2)(ω0T;ω0p,ω0id)Ap(z,t)Aid*(z,t)exp[i(Δk0zz+Δφ)]},
(z+1uidt)Aid(z,t)=iω0id2n0idc{χid(3)(ω0id;ω0pω0p,ω0id)Ap(z,t)2Aid(z,t)
+χid(2)(ω0id;ω0p,ω0T)Ap(z,t)AT*(z,t)exp[i(Δk0zz+Δφ)]},

where Δk0z = k p 0zk id 0zk T 0z; Δφ = φ 0pφ 0idφ 0T; ω 0m, nom and um (m = p,id,T) denote the angular frequencies, real refractive indices and the group velocities of the pump, idler and THz waves, respectively; the superscript ‘*’ denotes to make conjugation to the fields; χ (1) T is the linear ionic susceptibility at ω 0T; χ (2) is the sum of the second order electric and the ionic susceptibilities; χ (3) is known as Raman susceptibility [15].

The group velocities of the waves in a LN crystal are u p = 1.2673 × 108m/s for the pump wave at 1.064 µm and u T = 2.7693 × 107 m/s for the THz wave at 1 THz [16]. For a pump pulse with its width being τ p = 10ns, the walk-off length will be Ld = τ p/∣u -1 pu -1 T∣ = 135.6 cm, so that the walk-off effect in a LN crystal with a length of no more than twenty centimeters will generally be small. As a result, we can approximately take the pump, idler and THz waves to be of the same group velocity u. Thus we can convert Eq. (2) into a retarded time frame specified by

z=zandτ=tzu.

Because the pump wave is very strong while the THz wave is relatively much weaker, we can assume that the reduction in the pump wave intensity coming from nonlinear interaction could be ignored and then the amplitude of the pump wave can be regarded as a constant. As a result, the coupled wave Eqs. (2) can be reduced and one can obtain the solutions as

AT(z,τ)=1g+g{[βTAid*(0,τ)(gαT+iΔk0z2)AT(0,τ)]exp(g+z)
[βTAid*(0,τ)(g+αT+iΔk0z2)AT(0,τ)]exp(gz)}exp(iΔk0zz2),
Aid*(z,τ)=1g+g{[(g+αT+iΔkz2)Aid*(0,τ)+βid*AT(0,τ)]exp(g+z)
[(gαT+iΔkz2)Aid*(0,τ)+βid*AT(0,τ)]exp(gz)}exp(iΔk0zz2),
αT=iω0T2n0TccosφχT(1),
βT=iω0T2n0TccosφχT(2)Ap(0,τ)exp(iΔφ),
αid=iω0id2n0idccosθχid(3)Ap(0,τ)2,
βid=iω0id2n0idccosθχid(2)Ap(0,τ)exp(iΔφ),
g±=12(αT+αid*)±12(αT+αid*+iΔk0z)2+4βTβid*,

where A p (0,τ) = A p (z′ = 0,τ) is the initial complex envelop of the pump wave at the incident surface of the first crystal; A T (0,τ) and A id (0,τ) are the initial complex envelops of the THz and idler waves, respectively; θ is the angle between the pump wave and the idler wave; φ denotes the angle between the pump wave and the THz wave as shown in Fig. 1. Using Eq. (4), we may obtain the information of the idler and the THz waves at arbitrary position in the crystal in terms of the initial conditions.

Based on Eq. (4), we can obtain the expressions for the idler wave at the outgoing end of the two crystals in terms of the different initial conditions of the fields. For the first crystal, the initial conditions are A id (0,τ) = 0 and A T (0,τ) ≠ 0, then we obtain

Aid*(z,τ)=exp(g+z)exp(gz)g+gβid*AT(0,τ)exp(iΔk0zz2).

It should be pointed out that nearly all of the THz waves are absorbed due to the heavy absorption losses or are totally reflected by the right beveled side of the first crystal due to the large refractive index (greater than 5) in the THz range. Therefore, we assume that there are no THz waves propagating into the second crystal from the first crystal. Moreover, the LN crystals are transparent to the idler wave [7]. Thus, the initial conditions are A id (l 1,τ) ≠ 0 and A T (l 1,τ) = 0 for the second crystal. Thus we obtain

Aid*(z+l1,τ)=(g+αT+iΔkz2)exp(g+z)(gαT+iΔkz2)exp(gz)g+g
×Aid*(l1,τ)exp(iΔk0zz2),

where l 1 denotes the effective length of the first crystal. In the processes of deriving Eq. (6) and Eq. (7), the reflection and transmission losses of the idler wave at the interfaces of the two crystals are neglected. Introducing Eq. (6) into Eq. (7), we obtain the expression for the outgoing idler wave from the second crystal as

Aid*(l1+l2,τ)=iω0id2n0idccosθkχid(2)*Ap*(0,τ)AT(0,τ)exp{i[Δk0z2(l1+l2)+Δφ]},

where

κ=(g+αT+iΔk0z2)exp(g+l2)(gαT+iΔk0z2)exp(gl2)(g+g)2
×[exp(g+l1)exp(gl1)],

and l 2 represents the effective length of the second crystal.

The expressions for the electric field of the idler, pump and THz waves are E id (z′,τ) = A id (z′,τ)exp[−i(ω 0id τ + ϕ id)], E p (z′,τ) = A p (z′,τ)exp[−i(ω 0p τ + ϕ p)], and E T (z′,τ) = A T (z′,τ)exp[−i(ω 0T τ + ϕ T)], respectively, where ϕm=12k0zmz+φ0m (m = p,id,T) is the phase of the corresponding electric filed. From Eq. (8), we can obtain the expression of the electric field for the outgoing idler wave from the second crystal as

Eid*(l1+l2,τ)=iω0id2n0idccosθκχid(2)*Ep*(0,τ)ET(0,τ),

For the nanosecond pulses with slow varying envelopes, the time-dependent intensity I at position z′ can be approximately written as I (z′,τ) ≈ 2 0 nE(z′,τ)∣2 = 2 0 nA(z′,τ)∣2 [17,18]. Therefore, we obtain

Iid(l1+l2,τ)=ω0id28c3ε0n0pn0idn0Tcos2θκχid(2)*2Ip(0,τ)IT(0,τ).

Equations (10) and (11) build a bridge to connect the phase and intensity information between the incident THz wave and the measured idler wave, which are the main results for the time-dependent model presented in this work.

3. Numerical analyses

A LN crystal has four Raman- and infrared-active transverse optical phonon modes called A1-symmetry modes [19] and has a nonlinear coefficient d 33 = 25.2 µm/V at λ = 1.064 µm [20]. The expressions and data for the susceptibilities χ (1), χ (2) and χ (3) for the A1-symmetry modes can be taken from [9] and [21–23]. The refractive indices of the pump and idler waves can be obtained based on the Sellmeier equation for an extraordinary wave [24]. In general, the refractive index of THz waves in a LN crystal is a complex value. We write its real-part as

n0T=Reε+χi(1)(ω0T),

where ε is the high frequency dielectric constant.

The temporal envelops of the pulses are assumed to have a Gaussian form Am (z′,τ) = A 0m (z′)exp[−2ln2(τ/τm)2] (m = p,id,T), where A 0m and τm are the real peak field and the pulse width (full width at half maximum), respectively. The transverse spatial distribution of the pulse intensity is assumed to be uniform, and then the power of the pulse can be determined by multiplying the intensity by an effective spot area SA. Therefore, the time-dependent power of the pulse at z′ is Pm (z′,τ) = P 0m (z′)exp[−4ln2(τ/τm)2], here, the peak power P 0m (z′) ≈ Im (z′,0) SA = 2 0 n 0m SA[A 0m (z′)]2 (m = p,id,T). In addition, the energy of the pulse at a position z′ is simply determined by integrating the powers over time:

Wm(z)=Pm(z,τ)dτ=P0m(z)τmπ(2ln2).

Besides, we also assume that the three waves satisfy the so-called phase matched condition (Δk 0z′ = 0). By taking the system parameters close to the experimental ones reported in [4], we calculate the time-dependent power envelope of the wave pulses, as shown in Fig. 2. The calculated pulse width of the incident THz wave is τ T = 4.2 ns, which agrees well with the value (4.7 ns) of experimental one in [4]. The insert drawings are the initial pump pulse (left) and the measured idler pulse (right), respectively.

 figure: Fig. 2.

Fig. 2. The calculated time-dependent power envelope of the incident THz pulse with regard to an incident pump pulse (left insert drawing) and an output idler pulse (right insert drawing). The system parameters are τ p = 15 ns, λ p = 1.064 µm, τ id = 4.13 ns, λ id = 1.0697 µm, W p = 16 mJ, P 0id = 85 mW, SA = 1.3 × 1.1 mm2, l 1 = 5 mm and l 2 = 50 mm.

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 figure: Fig. 3.

Fig. 3. The curves of the incident THz pulse varying with the output idler wave with τ p = 15 ns, W p = 16 mJ, l 1 = 5 mm and l 2 = 50 mm. The blue one (left coordinate) is the curve between P 0T and P 0id with τ id = 4.13ns, while the red one (right coordinate) is the curve between τ T and τ id with P 0id = 85 mW.

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 figure: Fig. 4.

Fig. 4. The curves of the output idler pulse energy E id varying with the incident THz pulse energy E T under (a) different effective lengths of the first crystal, (b) different effective lengths of the second crystal, (c) different pulse energies of the incident pump beam, and (d) different pulse widths of the incident pump beam. The other system parameters are SA = 1.3 × 1.1 mm2, λ p = 1.064µm, τ T = 4 ns and ν 0T = ω 0T/2π = 1.5 THz.

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The energy input-output characteristics of the detector are investigated in detail. That is, the curves of the output idler pulse energy W id varying with the incident THz pulse energy W T are plotted under different system parameters. Figure 4 (a) shows the curves for different values of l 1 with l 2 = 50 mm, while Fig. 4(b) shows the curves for different values of l 2 with l 1 = 5 mm. Both Figs. 4(a) and 4(b) are corresponding to a given pump pulse with τ p = 15 ns and W p = 16 mJ. As might be expected, W id increases monotonically as the two effective lengths grow. Although the influence of the two effective lengths on W id is very small, it can be clearly seen from the illustrations within the Figs. 4(a) and 4(b). Furthermore, the impact of l 1 on W id is more significant than that of l 2. Therefore, one should pay more emphasis on elevating the length effective of the first crystal to achieve higher sensitivity. Figures 4(c) and 4(d) show the curves for different incident pump pulses with l 1 = 5 mm and l 2 = 50 mm, in which τ p = 15 ns for Fig. 4(c), while W p = 16 mJ for Fig. 4(d). As can be seen, Wid increases monotonically as W p increases and τ p decreases. Therefore, in order to effectively detect a THz wave, the energy and the duration of the pump pulse should be taken large and short enough. It should be noted that these conclusions are obtained based on the assumption of no pump depletion and out of consideration of other practical factors (e.g. photorefractive effect and noise) [4,25]. In spite of this, these results are still instructive for the parameters selections of an incident pump pulse.

Conclusions

We have presented a time-dependent theoretical model to describe the temporal behavior of a THz wave detector consisted of two pieces of LiNbO3 crystals. This model is suitable for the case that the electromagnetic waves are quasi-monochromatic nanosecond pulses. By taking the system parameters close to the experimental ones reported in [4], the calculated pulse width of the incident THz wave agrees well with the experiment one. The input-output characteristics of the detector are investigated and some conclusions, which could be useful for guiding and optimizing the design of the detector, are obtained. We believe that this study provides a strict theoretical basis for the highly sensitive coherent THz detector.

Appendix: Coupled wave equations for quasi-monochromatic pulses

From Maxwell equations the nonlinear scalar equation describing the propagation of the electric field of plane wave can be written as

2E=1ε0c22D(1)t2+1ε0c22PNLt2,

where D (1) = ε 0 E + P L, and P L is the linear polarization. We express the quantities in terms of their Fourier transform as

E(x,z,t)=E˜(x,z,ω)eiωtdω2π,
D(1)(x,z,t)=D˜(1)(x,z,ω)eiωtdω2π,
PNL(x,z,t)=P˜NL(x,z,ω)eiωtdω2π,

We assume that (1) (x,z,ω) and (x,z,ω) are related by the usual linear dispersion relation as

D˜(1)(x,z,ω)=ε0εr(ω)E˜(x,z,ω).

where εr (ω) is the relative dielectric constant with respect to ω.

By introducing these forms into Eq. (A1), we can obtain a relation for ω frequency component of the pulse in the frequency domain and which is given by

2E˜(x,z,ω)=ω2εr(ω)c2E˜(x,z,ω)ω2ε0c2P˜NL(x,z,ω).

Our goal is to derive a wave equation for slowly space and time varying field complex envelope A(x,z,t) defined by

E(x,z,t)=A(x,z,t)exp[i(ω0tk0xxk0zzφ0)]+c.c.,

where ω 0 is the angular frequency and k 0 is the linear part of the wave vector at ω 0, φ 0 is the real constant initial phase. c.c. denotes the complex conjugate. We represent A(x,z,t) in terms of its spectral content as

A(x,z,t)=A˜(x,z,ω)eiωtdω2π.

From Eqs. (A2)a), (A5) and (A6), we have

E˜(x,z,ω)=A˜(x,z,ωω0)exp[i(k0xx+k0zz+φ0)]
+A˜*(x,z,ω+ω0)exp[i(k0xx+k0zz+φ0)].

By using the quantity à (x,z,ω) (the slowly varying field amplitude in the frequency domain), the wave equation becomes

[2x2+2z2+2i(k0xx+k0zz)+k2(ω)k0x2k0z2]A˜(x,z,ωω0)
×exp[i(k0xx+k0zz+φ0)]+c.c.=ω2ε0c2P˜NL(x,z,ω),

where

k2(ω)=εr(ω)ω2c2.

We then expand k (ω) as a power series with respect to ω 0 as

k(ω)=k0+dk(ω)dωω0(ωω0)+high order dispersion.

We shall ignore the high order dispersion, which is permissible in the case of nanosecond pulses (the dispersion length is much greater than the distance of the nonlinear pulse interaction [10,11]). So we have

k2(ω)=k02+2k0u(ωω0)+1u2(ωω0)2,

where u = /dk (ω) is the group velocity of wave packet.

We now introduce k 2 (ω) into the wave equation, which then becomes

[2x2+2z2+2i(k0xx+k0zz)+2k0u(ωω0)+1u2(ωω0)2]A˜(x,z,ωω0)
×exp[i(k0xx+k0zz+φ0)]+c.c.=ω2ε0c2P˜NL(x,z,ω).

We convert this equation back to the time domain and obtain

[2x2+2z2+2i(k0xx+k0zz)+2ik0ut1u22t2]A(x,z,t)
×exp[i(k0xx+k0zz+φ0ω0t)]+c.c.=1ε0c22PNL(x,z,t)t2.

In our model, the directions of energy flows are the same to those of wave vectors. Because of the small angular between the pump wave and the idler wave, the x-direction component of energy flow for the idler wave is much smaller than that along z-direction (we choose the propagation direction of pump wave along z-direction). Thus we drop the quantities along x-direction. We also adopt the so-called slowly varying envelope approximation to Eq. (A13) and simplify this expression to obtain

2ik0z(z+1ut)A(z,t)exp[i(k0zz+φ0ω0t)]+c.c.=1ε0c22PNL(z,t)t2.

We next express the polarization in term of its slowly varying envelope p NL (z,t) as

PNL(z,t)=pNL(z,t)exp(iω0t)+c.c.

Then we obtain

2PNL(z,t)t2=(2t22iω0tω02)pNL(z,t)exp(iω0t)+c.c..

In the case of the pulse whose duration is much larger than its optical period, which can be satisfied for a nanosecond pulse in optical or THz range, we may neglect the first two terms on the right-hand side of Eq. (A16), and then this expression becomes

2PNL(z,t)t2=ω02pNL(z,t)exp(iω0t)+c.c..

By introducing Eq. (A17) into the wave equation in the form of Eq. (A14), we obtain

(z+1ut)A(z,t)=iω022k0zε0c2pNL(z,t)exp[i(k0zz+φ0)].

Acknowledgements

The National Natural Science Foundation of China under grant No. 10974063, the Research Foundation of Wuhan National Laboratory under Grant No. P080008, and the National “973” Project under Grant No. 2007CB310403 have supported this research. The authors thank the reviewers for their valuable comments and helpful suggestions on the quality improvement of our present work.

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Figures (4)

Fig. 1.
Fig. 1. Schematic diagrams (a) the THz wave detector made of two LN crystals reported in [4], and (b) wave configuration, boundary conditions and coordinate system.
Fig. 2.
Fig. 2. The calculated time-dependent power envelope of the incident THz pulse with regard to an incident pump pulse (left insert drawing) and an output idler pulse (right insert drawing). The system parameters are τ p = 15 ns, λ p = 1.064 µm, τ id = 4.13 ns, λ id = 1.0697 µm, W p = 16 mJ, P 0id = 85 mW, SA = 1.3 × 1.1 mm2, l 1 = 5 mm and l 2 = 50 mm.
Fig. 3.
Fig. 3. The curves of the incident THz pulse varying with the output idler wave with τ p = 15 ns, W p = 16 mJ, l 1 = 5 mm and l 2 = 50 mm. The blue one (left coordinate) is the curve between P 0T and P 0id with τ id = 4.13ns, while the red one (right coordinate) is the curve between τ T and τ id with P 0id = 85 mW.
Fig. 4.
Fig. 4. The curves of the output idler pulse energy E id varying with the incident THz pulse energy E T under (a) different effective lengths of the first crystal, (b) different effective lengths of the second crystal, (c) different pulse energies of the incident pump beam, and (d) different pulse widths of the incident pump beam. The other system parameters are SA = 1.3 × 1.1 mm2, λ p = 1.064µm, τ T = 4 ns and ν 0T = ω 0T/2π = 1.5 THz.

Equations (51)

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( z + 1 u t ) A ( z , t ) = i ω 0 2 2 k 0 z ε 0 c 2 p NL ( z , t ) exp [ i ( k 0 z z + φ 0 ) ] ,
( z + 1 u p t ) A p ( z , t ) = i ω 0 p 2 n 0 p c { χ p ( 3 ) ( ω 0 p ; ω 0 p ω 0 id , ω 0 id ) A id ( z , t ) 2 A p ( z , t )
+ χ p ( 2 ) ( ω 0 p ; ω 0 id , ω 0 T ) A id ( z , t ) A T ( z , t ) exp [ i ( Δ k 0 z z + Δ φ ) ] } ,
( z + 1 u T t ) A T ( z , t ) = i ω 0 T 2 n 0 T c { χ T ( 1 ) ( ω 0 T ) A T ( z , t )
+ χ T ( 2 ) ( ω 0 T ; ω 0 p , ω 0 id ) A p ( z , t ) A id * ( z , t ) exp [ i ( Δ k 0 z z + Δ φ ) ] } ,
( z + 1 u id t ) A id ( z , t ) = i ω 0 id 2 n 0 id c { χ id ( 3 ) ( ω 0 id ; ω 0 p ω 0 p , ω 0 id ) A p ( z , t ) 2 A id ( z , t )
+ χ id ( 2 ) ( ω 0 id ; ω 0 p , ω 0 T ) A p ( z , t ) A T * ( z , t ) exp [ i ( Δ k 0 z z + Δ φ ) ] } ,
z = z and τ = t z u .
A T ( z , τ ) = 1 g + g { [ β T A id * ( 0 , τ ) ( g α T + i Δ k 0 z 2 ) A T ( 0 , τ ) ] exp ( g + z )
[ β T A id * ( 0 , τ ) ( g + α T + i Δ k 0 z 2 ) A T ( 0 , τ ) ] exp ( g z ) } exp ( i Δ k 0 z z 2 ) ,
A id * ( z , τ ) = 1 g + g { [ ( g + α T + i Δ k z 2 ) A id * ( 0 , τ ) + β id * A T ( 0 , τ ) ] exp ( g + z )
[ ( g α T + i Δ k z 2 ) A id * ( 0 , τ ) + β id * A T ( 0 , τ ) ] exp ( g z ) } exp ( i Δ k 0 z z 2 ) ,
α T = i ω 0 T 2 n 0 T c cos φ χ T ( 1 ) ,
β T = i ω 0 T 2 n 0 T c cos φ χ T ( 2 ) A p ( 0 , τ ) exp ( i Δ φ ) ,
α id = i ω 0 id 2 n 0 id c cos θ χ id ( 3 ) A p ( 0 , τ ) 2 ,
β id = i ω 0 id 2 n 0 id c cos θ χ id ( 2 ) A p ( 0 , τ ) exp ( i Δ φ ) ,
g ± = 1 2 ( α T + α id * ) ± 1 2 ( α T + α id * + i Δ k 0 z ) 2 + 4 β T β id * ,
A id * ( z , τ ) = exp ( g + z ) exp ( g z ) g + g β id * A T ( 0 , τ ) exp ( i Δ k 0 z z 2 ) .
A id * ( z + l 1 , τ ) = ( g + α T + i Δ k z 2 ) exp ( g + z ) ( g α T + i Δ k z 2 ) exp ( g z ) g + g
× A id * ( l 1 , τ ) exp ( i Δ k 0 z z 2 ) ,
A id * ( l 1 + l 2 , τ ) = i ω 0 id 2 n 0 id c cos θ k χ id ( 2 ) * A p * ( 0 , τ ) A T ( 0 , τ ) exp { i [ Δ k 0 z 2 ( l 1 + l 2 ) + Δ φ ] } ,
κ = ( g + α T + i Δ k 0 z 2 ) exp ( g + l 2 ) ( g α T + i Δ k 0 z 2 ) exp ( g l 2 ) ( g + g ) 2
× [ exp ( g + l 1 ) exp ( g l 1 ) ] ,
E id * ( l 1 + l 2 , τ ) = i ω 0 id 2 n 0 id c cos θ κ χ id ( 2 ) * E p * ( 0 , τ ) E T ( 0 , τ ) ,
I id ( l 1 + l 2 , τ ) = ω 0 id 2 8 c 3 ε 0 n 0 p n 0 id n 0 T cos 2 θ κ χ id ( 2 ) * 2 I p ( 0 , τ ) I T ( 0 , τ ) .
n 0 T = Re ε + χ i ( 1 ) ( ω 0 T ) ,
W m ( z ) = P m ( z , τ ) d τ = P 0 m ( z ) τ m π ( 2 ln 2 ) .
2 E = 1 ε 0 c 2 2 D ( 1 ) t 2 + 1 ε 0 c 2 2 P NL t 2 ,
E ( x , z , t ) = E ˜ ( x , z , ω ) e i ω t d ω 2 π ,
D ( 1 ) ( x , z , t ) = D ˜ ( 1 ) ( x , z , ω ) e i ω t d ω 2 π ,
P NL ( x , z , t ) = P ˜ NL ( x , z , ω ) e i ω t d ω 2 π ,
D ˜ ( 1 ) ( x , z , ω ) = ε 0 ε r ( ω ) E ˜ ( x , z , ω ) .
2 E ˜ ( x , z , ω ) = ω 2 ε r ( ω ) c 2 E ˜ ( x , z , ω ) ω 2 ε 0 c 2 P ˜ NL ( x , z , ω ) .
E ( x , z , t ) = A ( x , z , t ) exp [ i ( ω 0 t k 0 x x k 0 z z φ 0 ) ] + c . c . ,
A ( x , z , t ) = A ˜ ( x , z , ω ) e i ω t d ω 2 π .
E ˜ ( x , z , ω ) = A ˜ ( x , z , ω ω 0 ) exp [ i ( k 0 x x + k 0 z z + φ 0 ) ]
+ A ˜ * ( x , z , ω + ω 0 ) exp [ i ( k 0 x x + k 0 z z + φ 0 ) ] .
[ 2 x 2 + 2 z 2 + 2 i ( k 0 x x + k 0 z z ) + k 2 ( ω ) k 0 x 2 k 0 z 2 ] A ˜ ( x , z , ω ω 0 )
× exp [ i ( k 0 x x + k 0 z z + φ 0 ) ] + c . c . = ω 2 ε 0 c 2 P ˜ NL ( x , z , ω ) ,
k 2 ( ω ) = ε r ( ω ) ω 2 c 2 .
k ( ω ) = k 0 + dk ( ω ) d ω ω 0 ( ω ω 0 ) + high order dispersion .
k 2 ( ω ) = k 0 2 + 2 k 0 u ( ω ω 0 ) + 1 u 2 ( ω ω 0 ) 2 ,
[ 2 x 2 + 2 z 2 + 2 i ( k 0 x x + k 0 z z ) + 2 k 0 u ( ω ω 0 ) + 1 u 2 ( ω ω 0 ) 2 ] A ˜ ( x , z , ω ω 0 )
× exp [ i ( k 0 x x + k 0 z z + φ 0 ) ] + c . c . = ω 2 ε 0 c 2 P ˜ NL ( x , z , ω ) .
[ 2 x 2 + 2 z 2 + 2 i ( k 0 x x + k 0 z z ) + 2 i k 0 u t 1 u 2 2 t 2 ] A ( x , z , t )
× exp [ i ( k 0 x x + k 0 z z + φ 0 ω 0 t ) ] + c . c . = 1 ε 0 c 2 2 P NL ( x , z , t ) t 2 .
2 ik 0 z ( z + 1 u t ) A ( z , t ) exp [ i ( k 0 z z + φ 0 ω 0 t ) ] + c . c . = 1 ε 0 c 2 2 P NL ( z , t ) t 2 .
P NL ( z , t ) = p NL ( z , t ) exp ( i ω 0 t ) + c . c .
2 P NL ( z , t ) t 2 = ( 2 t 2 2 i ω 0 t ω 0 2 ) p NL ( z , t ) exp ( i ω 0 t ) + c . c . .
2 P NL ( z , t ) t 2 = ω 0 2 p NL ( z , t ) exp ( i ω 0 t ) + c . c . .
( z + 1 u t ) A ( z , t ) = i ω 0 2 2 k 0 z ε 0 c 2 p NL ( z , t ) exp [ i ( k 0 z z + φ 0 ) ] .
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