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. 2021 Mar 25;23(4):393. doi: 10.3390/e23040393

Auto- versus Cross-Correlation Noise in Periodically Driven Quantum Coherent Conductors

Michael Moskalets 1
Editor: Dario Ferraro1
PMCID: PMC8066600  PMID: 33806199

Abstract

Expressing currents and their fluctuations at the terminals of a multi-probe conductor in terms of the wave functions of carriers injected into the Fermi sea provides new insight into the physics of electric currents. This approach helps us to identify two physically different contributions to shot noise. In the quantum coherent regime, when current is carried by non-overlapping wave packets, the product of current fluctuations in different leads, the cross-correlation noise, is determined solely by the duration of the wave packet. In contrast, the square of the current fluctuations in one lead, the autocorrelation noise, is additionally determined by the coherence of the wave packet, which is associated with the spread of the wave packet in energy. The two contributions can be addressed separately in the weak back-scattering regime, when the autocorrelation noise depends only on the coherence. Analysis of shot noise in terms of these contributions allows us, in particular, to predict that no individual traveling particles with a real wave function, such as Majorana fermions, can be created in the Fermi sea in a clean manner, that is, without accompanying electron–hole pairs.

Keywords: single-electron wave packet, shot noise, quantum transport

1. Introduction

Recently, the quantum tomography of a single-electron wave function was demonstrated experimentally [1,2]. In both experiments, a periodic stream of single-electron wave packets was mixed with a low-amplitude electrical probe signal at the electron wave splitter, a quantum point contact, and the resulting electrical noise averaged over long time was measured. However, if the fluctuations of an electrical current within one output lead were measured in one experiment, the correlations of currents flowing within both output leads were measured in another. In a sense, these works are the culmination of a number of recent works where the cross-correlation noise was measured to count electrons emitted per period [3,4] to demonstrate a tunable fermionic anti-bunching [4,5,6,7], and the auto-correlation noise at high [8,9] and low [10,11] frequencies was measured to identify a single-electron emission regime. These experimental advances motivate us to take a closer look at how exactly the quantum properties of wave packets manifest themselves in the measured electrical noise [12,13,14].

Note that tomography of the density profile of solitary electrons was successfully realized in [15] using the measurement of the electrical current rather than noise.

Here, in contrast to previous works [16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32]—for a review, see in [33]—I will focus on comparing auto- and cross-correlation noise. I will show that, in the case of a periodic train of non-overlapping single-electron wave packets scattered off the wave splitter with reflection probability R, there are two contributions to noise. These contributions can be addressed separately by measuring both auto- and cross-correlation noise in the weak back-scattering regime, R1. As I will show in the subsequent sections, for a single-electron wave packet Ψt,x=eiμtψt,x injected during one period into a one-dimensional chiral Fermi sea and reflected into a detector at a wave splitter, see Figure 1, the auto-correlation, Pautoex, and cross-correlation, Pcross, noise power, see Equation (10), at frequency ω and at zero temperature are calculated as follows:

Pautoexω=Re2T0dτeiωτImCτπτ,Pcrossω=Re2T0Nω2, (1)

where the superscript ex (unnecessary for cross-correlation noise) indicates the excess over the equilibrium value, e is an electron charge, T0 is a period, Cτ is the integrated over time coherence of the wave function envelope, [34,35]

Cτ=dtψ*t+τ,xDψt,xD, (2)

and Nω is the Fourier transform of the wave packet density,

Nω=dτeiωτψτ,xD2. (3)

Figure 1.

Figure 1

Shot noise, see Equation (10), of a single-electron wave packet injected on top of the Fermi sea consists of two parts: One is determined by the density profile of the wave packet, shown as a filled hump, and the other is determined by both the coherence of the wave packet, shown as a double hump, and the Fermi sea, shown as a blue line. While the former contributes to both auto-correlation noise, Pauto, and cross-correlation noise, Pcross, the latter contributes to Pauto only. The solid arrow indicates the wave packet in incoming channel β=1, shown as an empty hump. The filled circle represents the wave splitter with reflection probability R and transmission probability T=1R. The two dashed arrows point to the two outgoing leads α=3 and α=4.

In Equations (2) and (3), xD is the coordinate of the detector used to measure the current. For simplicity, I assume that the coordinates of both detectors in the outgoing channels α=3 and α=4 are the same. Below, I discard xD and use the following notation: Ψ(t)Ψ(t,xD).

Equation (1) is the main result of this work, which shows us that in the weak backscattering regime, the auto-correlation noise and cross-correlation noise are determined by essentially different quantities. One can say that they provide somehow complementary information. The cross-correlation noise is sensitive merely to the shape of a wave packet, that is, to its duration in time, while the auto-correlation noise is rather sensitive to how different parts of the wave packet correlate with each other. Such correlations are related to the spread of the wave packet in energy, which is supported by the reasoning in [9] that only those particles whose energy exceeds the Fermi energy by more than ω contribute to the auto-correlation noise at the frequency ω.

Below, I use three known wave functions of particles injected into the Fermi sea by various electronic sources and calculate the corresponding auto- and cross-correlation noise in accordance with Equation (1). These results provide additional evidence of the duality of the information provided by both types of noise.

A Lorentzian voltage pulse, one per period, eV(t)=2Γτt2+Γτ21, applied to the Fermi sea with energy μ and at zero temperature creates a single-electron wave packet [36,37], named a leviton [4]. This excitation should be understood in such a way that the voltage pulse shakes the Fermi sea and excites just a single electron on its surface [38]. The wave function of a leviton, ΨL(t)=eiμtψL(t), has the following envelope function [39],

ψL(t)=1πΓτΓτtiΓτ. (4)

Here, the subscript τ indicates that Γτ is the half-width of the wave packet in time. I assume ΓτT0 to avoid overlap between the successive wave packets.

Using the above equation in Equation (1), I calculate

Pautoex,Lω=PcrossLω=Re2T0eω2Γτ. (5)

The fact that the auto- and cross-correlation noise show the same frequency dependence is because there is only one time parameter in the problem, Γτ, which defines both the characteristic energy of the wave packet, /2Γτ [39], and the characteristic width in time of the wave packet, 2Γτ.

In the next example, the shape and the energy distribution are not related so tight and Pautoexω and Pcrossω become different.

Let us consider a quantum level of half-width δ filled with one electron and tunnel-coupled to a one-dimensional Fermi sea at zero temperature. The energy of a level raises at a constant rapidity c, and crosses the Fermi level at t=0 when an electron is injected into the Fermi sea. Such regime of injection can be realized using the quantum capacitor [40,41,42]. The wave function of the injected electron was calculated in [43], Ψc(t)=eiμtψc(t), with

ψ(c)t=1πΓτ0dxexeixtΓτeix2τDΓτ, (6)

where Γτ=δ/c is the crossing time, the time it takes for a raising widened quantum level to cross the Fermi level, τD=/2δ is the dwell time, an average time spent an electron on a quantum level before escaping to the Fermi sea provided that such an escape is possible, that is, after the quantum level has risen above the Fermi level. Note that if τDΓτ, then ψc, Equation (6), is essentially ψL, Equation (4). Notice, to get a stream of electrons we need a set of levels. Subsequent crossings occur with a delay of T0Γτ,τD. Now Equations (1) and (6) give us

Pautoex,c(ω)=Re2T0eω2Γτ,Pcrossc(ω)=Re2T0eω2Γτ1+ωτD2. (7)

For this model, the crossing time 2Γτ is the only parameter that determines the energy distribution, the same as for the source of levitons [44]. This is why the auto-correlation noise is the same as in the first example.

However, the shape of the wave packet is different from that of a leviton. It is determined by both time parameters Γτ and τD. Namely, if the dwell time is comparable with the crossing time, τDΓτ, the density profile becomes larger than 2Γτ, asymmetric, and with some wavy structure developing at later times. All this leads to additional suppression of Nω and Pcrossc(ω) with increasing frequency compared to the first example. In the case when τDΓτ, the dwell time, not the crossing time, determines how the cross-correlation noise decreases with frequency.

The connection between the auto-correlation noise and energy becomes even more transparent in the final example, where the dwell time is the only characteristic time.

The final (third) example is injection from a quantum dot with the equidistant ladder of levels, which is suddenly raised by one level spacing Δ at t=0 [42,45]. The Fermi level is exactly between the two successive levels. The probability of tunneling between the dot and the Fermi sea is small. The wave function, ΨΔ(t)=eiμtψΔ(t), has an envelope [35,46]

ψΔ(t)=θ(t)eiω0tτDet2τD. (8)

Here, θ(t) is the Heaviside step function and ω0=Δ/2. Notice, in this case, the wave packet width is determined by the dwell time, while the energy of an injected electron is ω0, which is unrelated to τD.

For not too large frequencies, ωΔ/, the straightforward calculations based on Equation (1) lead to the following result (see Appendix A for details):

Pautoex,Δ(ω)=Re2T0,PcrossΔ(ω)=Re2T011+ωτD2. (9)

As the particles are injected far above the Fermi sea, Δ/2ω, all of them contribute to noise. As a result, there is no energy related suppression (for ωΔ/ and R1). Therefore, the auto-correlation noise is independent on frequency. On the other hand, the density profile has a finite width, τD. Therefore, the cross-correlation noise gets suppressed at ωτD1.

One more important conclusion can be drawn from Equation (1). In the case when a single-particle envelope wave function, ψ, is real-valued, for example, as for Majorana fermions [47,48], the corresponding contribution to the auto-correlation noise is identically zero in the weak backscattering regime. I emphasize that this conclusion applies to traveling single particles in the Fermi sea, and not to localized states.

For some injection protocols the auto-correlation noise is also zero for R=1, see in [49].

Note that the charge conservation implies Pautoex0+Pcross0=0, see Appendix B.3 [14]. This fact imposes some indirect constraint on the wave function of a single-electron wave packet that can be injected into a one-dimensional Fermi sea. In particular, no single particle with a real wave function can be injected in a clean manner, that is, without accompanying electron–hole pairs. Indeed, as Equation (1) predicts, the cross-correlation noise at zero frequency is not zero, Pcross0=Re2/T00. While in the case of a real-valued wave function, the excess auto-correlation noise vanishes for any frequency, Pautoexω=0. To eliminate the apparent violation of charge conservation and ensure Pautoex0=Pcross00, we must assume that if such a particle is injected, then the additional excitations are unavoidable created. The example is a half-leviton [50], a particle with a real wave function whose creation is accompanied by the creation of an electron–hole cloud.

The rest of the paper is structured as follows. In Section 2, within the framework of the Floquet scattering matrix approach, a connection is established between the correlation functions of the electrical current, the auto- and cross-correlation noise power, and the first-order correlation function of a periodic stream of electrons injected into a chiral Fermi sea. This relationship allows a detailed analysis of the similarities and differences between auto- and cross-correlation noise, which is illustrated in Section 3 using some examples. The conclusion is given in Section 4. Some technical details of calculations are presented in Appendix A, Appendix B, Appendix C and Appendix D.

2. Electrical Noise and Electron Correlation Function

In general, an external source is required to pass current through a conductor. The role of the source can be played, for example, by a constant or time-dependent voltage applied across a conductor; a time-dependent gate voltage, which changes the position of the quantum levels of electrons in a part of the conductor; etc. If the characteristics of the source are known, the current can be calculated. In the quantum coherent regime, when the current is carried by individual electrons, the characteristics of carriers, for example, their wave function, also can be calculated using the characteristics of the source. The measurements of electrical current and its fluctuations were already used to acquire information on quantum state of carriers [1,2,15]. Therefore, it is desirable to have a direct relation between the electrical and electron characteristics without explicit recursion to the characteristics of the source. Some efforts in this direction have already been made [44,50,51,52]. Below the fluctuations of an electrical current are expressed in terms of the wave functions, more precisely, in terms of the excess first-order correlation function [17,18,35,46] of electrons responsible for those fluctuations.

To be specific, here I am interested in a quantum coherent conductor connected via one-channel (chiral) leads [53] to several electron reservoirs in equilibrium. Some (or all) incoming leads are fed by external sources working periodically with period T0.

Below, I use the theory of non-interacting electrons. This is justified by the fact that such a theory has proved useful in describing the injection of single electrons [4,42], the results of quantum tomography of single electrons [1,2], and, in particular, the frequency-dependent noise [8,9] of interest here.

2.1. Frequency-Dependent Noise

The correlation function of currents, Iα,Iα, flowing in leads α and α of a multi-terminal conductor are defined as follows [14]:

Pααω=0T0dtT0dτeiωτI^α(t+τ)I^α(t)+I^α(t)I^α(t+τ)2Iα(t+τ)Iα(t), (10)

where I^α and Iα=I^α are an operator in second quantization and a corresponding measurable for a current in the lead α; the angular brackets denote the quantum statistical average; for a periodic drive, T0 is a period, for a non-periodic drive T0. Note the difference in the factor of 2 compared to the definition used in [14].

The current operator I^α is expressed in terms of creation and annihilation operators a^α(E),a^α(E) of electrons with energy E incoming from the reservoir α and operators b^α(E),b^α(E) of electrons with energy E scattered into the reservoir α [54]. In the wide band limit, that is, when the relevant energy scales, such as a voltage applied, a temperature, the energy quantum Ω with Ω=2π/T0, etc., are all small compared to the Fermi energy μα, the current operator reads [55],

I^α(t)=ehdEdEeiEEtb^α(E)b^α(E)a^α(E)a^α(E). (11)

In the case of a periodically driven conductor, the operators b^α are related to various operators a^α via the elements of the unitary Floquet scattering matrix SF [56],

b^αE=βn=SF,αβE,Ena^βEn, (12)

where the short notation En=E+nΩ is introduced. Charge conservation requires the scattering matrix to be unitary, which means

γn=SF,γα*En,EmSF,γβEn,E=δαβδm,0,γn=SF,αγ*Em,EnSF,βγE,En=δαβδm,0, (13)

where δn,0 is the Kronecker delta.

Equation (12) allows to express the quantum-statistical average of the product of b-operators in terms of that of a-operators. Because the reservoirs are in equilibrium, the latter average is known. In the case of reservoirs of non-interacting electrons forming the Fermi sea, we have a^β(E)a^β(E)=fβ(E)δEE, where fβ(E) is the Fermi distribution function with temperature θβ and chemical potential μβ, and δEE is the Dirac delta.

2 × 2 Circuit

Our aim is to compare auto- and cross-correlation noise. The minimal circuit that allows cross-correlation noise is an electronic wave splitter, a quantum point contact (QPC) with two incoming, β=1,2, and two outgoing, α=3,4, channels, see Figure 1.

Below, I am interested in current fluctuations in outgoing channels, that is, α,α=3,4 in Equation (10). For this case, the general equation for noise within the Floquet scattering matrix approach [57,58] gives us

P33ω=e2hdE{F33(E,E+ω)+n,m,q=δ=12γ=12Fγδ(Eq+ω,E)×SF,3δ*(En,E)SF,3δ(Em,E)SF,3γ*(Em+ω,Eq+ω)SF,3γ(En+ω,Eq+ω)}, (14a)

and

P34(ω)=e2hdEn,m,q=δ=12γ=12Fγδ(Eq+ω,E)SF,3δ*(En,E)SF,4δ(Em,E)×SF,4γ*(Em+ω,Eq+ω)SF,3γ(En+ω,Eq+ω), (14b)

with

Fγδ(E1,E)=fγE1+fδE2fγE1fδE. (15)

Let us also introduce excess noise, that is, an increase in noise due to the source, which is defined as the following difference:

Pααexω=PααωPααoffω, (16)

where the upper index off indicates that the source is switched off.

I suppose a unitary 2×2 scattering matrix of the QPC to be energy-independent,

SQPC=RiTiTR, (17)

a real number 0R1 is the reflection probability, the transmission probability T=1R. We need an energy independent SQPC in order to use noise to get information on injected wave packets only. If the properties of the electronic circuit that connects the incoming and outgoing channels do depend on energy, the outgoing signal also carries nontrivial information about the circuit [59].

In addition, for the sake of simplicity, I suppose that the periodic source is present only in the incoming channel β=1. This source characterized by the Floquet scattering amplitude, which is a matrix in an energy space with elements SFE,En. The results presented below can be directly generalized to the case when another source is added in the second incoming channel, see Appendix B.4.

For the circuit with single source and single QPC, the elements of the total Floquet scattering matrix are represented as follows:

SF,31E,En=RSFE,En,SF,41E,En=iTSFE,En,SF,32E,En=iTδn,0,SF,42E,En=Rδn,0. (18)

All other elements are zero.

2.2. First-Order Correlation Function

To characterize a quantum state injected by the source into a ballistic one-dimensional electronic waveguide, I use the first-order correlation function, G(1). This function is defined as a quantum statistical average of the product of two field operators for electrons calculated in the electronic wave-guide β just after the source, Gβ(1)t1;t2=Ψ^β(t1)Ψ^β(t2) [17]. Strictly speaking, this object is a 2×2 matrix in the spin space. However, here I consider the spin-polarized case and suppress the spin index.

When the source is placed in lead β=1 and is characterized by the Floquet scattering amplitude, SFEn,E, the corresponding correlation function is calculated as follows [51]:

vμG1(1)(t+τ;t)=1hdEf1EeiEτn,m=eiΩnτeiΩnmtSF*En,ESFEm,E. (19)

Here, vμ is a velocity of electrons at the Fermi level, which is originated from the density of states being energy independent in the wide band limit used here.

When the source is switched off, SFEn,E=δn,0, the above equation is reduced to the correlation function of the Fermi sea in equilibrium, which depends on the difference of times rather than on two times separately. I denote the equilibrium correlation function by the complementary subscript 0 and obtain for lead β, G0,β(1)(τ)G0,β(1)(t+τ;t)

vμG0,β(1)(τ)=1hdEfβEeiEτ=eiτμβ2πi1/τθβsinhτ/τθβ. (20)

Here, τθβ=/(πkBθβ) is the thermal coherence time for the reservoir, where the lead β is attached to.

The difference of correlation functions with the source being on and off is the excess correlation function, which characterizes what is injected by the source into an electron waveguide β=1 [18],

G1(1)t1;t2=G1(1)t1;t2G0,1(1)t1t2. (21)

In the case when the source injects a single electron with wave function Ψ(t) per period, the excess correlation function during that period takes on a very simple form, G1(1)t1;t2=Ψ*t1Ψt2. In the case of injection of N electrons, G1(1)t1;t2=j=1NΨj*t1Ψjt2 [63].

2.3. Noise Power in Terms of G(1)

For non-interacting electrons, the correlation function G(1) contains complete information about the system of electrons. In particular, all measurables can be expressed in terms of correlation function, see, e.g., in [51] for some examples. Such expressions are notably useful when transport is due to only a few electrons per period.

Here, I express the excess noise in terms of G(1) in the case when all incoming channels have the same temperature θβ=θ and Fermi energy μβ=μ. Therefore, the equilibrium electronic correlation functions are the same, G0,β(1)=G0(1). For more general case and for details of calculations, see Appendix B.

First, let us substitute Equations (15) and (18) into Equations (14a) and (14b) and calculate the excess noise, Equation (16). As a result, I find for the auto-correlation noise (see Equation (A20)),

P33exω=e2vμ20T0dtT0dτeiωτR2G1(1)t+τ;t22RReG1(1)t+τ;tG0(1)*τ, (22a)

and for the cross-correlation noise (see Equation (A18)),

P34(ω)=RTe2vμ20T0dtT0dτeiωτG1(1)t+τ;t2. (22b)

The above equations are the central result of this work.

Notice that when all reservoirs are in the same conditions, cross-correlation noise disappears when the source is turned off. This is why the superscript ex is omitted.

The important difference between auto- and cross-correlation noise (Equations (22a) and (22b)) is that the latter is determined solely by what is injected by the source, while the former in addition depends explicitly on the properties of the Fermi sea.

The part of the noise that is determined by G1(1)2 depends on the possible quantum exchange [14] between the injected electrons. At zero temperature and when electrons are injected one at a time without overlapping, this part of the noise is reduced to the product of currents in Equation (10). In the wide band approximation used here, the electric current is proportional to the density profile of the wave packet, hence Equation (1), the second line.

In contrast, the part of the noise that is determined by the product of G1(1) and G0(1) takes into account the quantum exchange of an injected electron and electrons of the Fermi sea. Such an exchange does not contribute to cross-correlation noise, unless the two incoming Fermi seas are different, see Equation (A23).

The formal difference between the auto- and cross-correlation noise becomes especially pronounced in the weak back-scattering regime, R1, when we can discard the terms R2 in Equations (22a) and (22b) and get the following,

P33exω=Re2vμ20T0dtT0dτeiωτ2ReG1(1)t+τ;tG0(1)*τ,P34(ω)=Re2vμ20T0dtT0dτeiωτG1(1)t+τ;t2. (23)

Notice that using Equation (20) for G0(1) at zero temperature, θ=0τθ, and for a single-particle injection, G(1)t+τ;t=eiμτψ*t+τψ(t), we arrive at Equation (1) with Pautoex=P33ex and Pcross=P34, where integration over t is extended to infinity, as the duration of the wave packet is much less than the period T0.

3. Examples

In this section, I will consider two examples: one when auto- and cross-correlation noise are perfectly anti-correlated at any frequency, and the other when they can be different. The corresponding equations are valid for arbitrary R, and not only for R1, as in the examples given in the introductory section.

3.1. Energy-Independent Source

In the case when the properties of the source do not change on the scale of the energy of the injected particles, the corresponding Floquet scattering amplitude can be represented as a Fourier coefficient of a certain energy-independent scattering amplitude, SFEn,E=0T0dtT0e2πintT0S(t) [46,56]. In a one-dimensional case, unitarity implies that S(t) is a pure phase factor, that is, S(t)2=1. For example, if a voltage V(t) plays the role of a source, then this phase factor reads S(t)=expietdtV(t).

In such a case, Equation (19) gives us G1(1)(t1;t2)=S*(t1)S(t2)G0,1(1)(t1t2). Note that G0,1(1) describes the Fermi sea in equilibrium at temperature θ1. Using this result in Equations (22a) and (22b), and taking into account that

G1(1)(t1;t2)=S*(t1)S(t2)1G0,1(1)(t1t2), (24)

we find that the excess auto- and cross-correlation noise are perfectly anti-correlated at any frequency,

P33exω+P34ω=0, (25)

not only at zero frequency, ω=0, as the charge conservation requires [14]. An example was shown in Equation (5).

For R=1, when cross-correlation noise does not exist, that is, formally P34=0, the above equation tells us that whatever emitted by the source under consideration is silent on any frequency, the excess auto-correlation noise is zero, P33exω=0. In particular, any voltage applied to a ballistic channel produces no excess noise at any frequency. Note that for a generic source injecting electrons into a ballistic waveguide, a similar conclusion can be drawn for noise only at zero frequency, see Equation (A25). Note that in the case of R=1, zero excess auto-correlation noise tells us nothing about the number of excited particle–hole pairs. In order to count the number of excitations, we need a wave-splitter with R<1.

Some general conclusions can be made regarding the effect of temperature on noise. Indeed, Equations (20) and (24) allow us to relate the excess correlation function at zero (the extra subscript 0) and non-zero (the extra subscript θ) temperatures as follows:

G1,θ(1)t+τ;t=τ/τθsinhτ/τθG1,0(1)t+τ;t. (26)

Then, I use the above equation in Equations (22a) and (22b), utilize the inverse Fourier transformation with respect to ω, and express the noise at temperature θ, Pθex, in terms of the noise at zero temperature, P0ex, as follows,

Pθexω=dτeiωττ/τθsinhτ/τθ2dω2πeiωτP0exω. (27)

Here, I introduce PexP33ex=P34 according to Equation (25).

3.2. Injection from a Quantum Level Raising at a Constant Rapidity

Now, let us consider a single-electron injection from a source, whose properties depend on energy. The corresponding scattering amplitude and the wave function of the injected electron were discussed in [43] at zero temperature and in [60] at nonzero temperatures. In this case, the auto- and cross-correlation noises do not stick together unless at zero frequency.

At zero temperature, the excess correlation function is vμG1(1)t+τ;t=eiμτψ(c)*t+τψ(c)t, where ψ(c) is shown in Equation (6). Using this equation in Equations (22a) and (22a) and assuming that the width of the wave packet is small compared to the period, maxΓτ,τDT0, I find (see Appendix C for details),

P33ex(ω)=Re2T0T+ωτD21+ωτD2eω2Γτ,P34(ω)=Re2T0T1+ωτD2eω2Γτ. (28)

At R1 (T1), Equation (7) is reproduced.

The above equations are illustrated in Figure 2 in the case of 2ΓττD, when the difference between them is most pronounced. As I have already discussed in the introduction after Equation (7), the excess auto-correlation noise and the cross-correlation noise demonstrate significantly different dependencies on frequency. The cross-correlation noise (its absolute value) decreases monotonically with frequency, see Figure 2, a red dashed line. In contrast, the excess auto-correlation noise is non-monotonically dependent on frequency, which is a manifestation of the existence of two contributions. The first contribution, which is responsible for the quadratic increase at low frequencies, is similar to the cross-correlation noise, compare the first term in Equations (22a) and (22b), while the second contribution is different. This contribution dominates in the limit of T1 and at high frequencies, see a black solid line in Figure 2.

Figure 2.

Figure 2

The excess auto- (solid lines) and cross-correlation (a red dashed line) noise is shown as a function of the frequency ω at zero temperature, see Equation (28). The cross-correlation noise, PP34, is given in units of RTe2/T0. The excess auto-correlation noise, PP33ex, is given in units of Re2/T0 for T=0.999 (a black line), T=0.7 (a blue line), T=0.4 (a green line), and T=0.1 (an orange line). The parameter 2Γτ/τD=0.1.

At non-zero temperature, θ>0, auto- and cross-correlation noise is modified by the same factor, P33,θex(ω)=ηω,θP33ex(ω) and P34,θ(ω)=ηω,θP34(ω) (see Appendix D for details), where

ηω,θ=eω2Γτdxπeixω2Γτx2+1x2Γτ/τθsinhx2Γτ/τθ2. (29)

The thermal coherence time τθ is defined after Equation (20).

Interestingly, the above equation is independent of the dwell time τD=/2Γτc, where c is a rapidity, see Equation (6). Therefore, the same factor ηω,θ applies for the case of τD=0, which is the case for the source of levitons of half-width Γτ. However, this analogy is not complete.

Namely, for the case of levitons, the noise at non-zero temperatures can be expressed directly in terms of the noise at zero temperature, see Equation (27). On the contrary, for the case of electrons emitted from the quantum level, this is generally not the case due to factors that depend on ωτD. Yet, in the weak backscattering regime, R1, the auto-correlation noise obeys Equation (27), because it has no such factors, see Equation (7).

The temperature-dependent factor ηω,θ, Equation (29), is shown in Figure 3 for several frequencies ω. Remarkably, the maximum occurs at ωτθ1, which is independent of properties of the source. The non-monotonic temperature behavior at non-zero frequencies is due to two counteracting effects, both due to the fact that the quantum state of electrons injected at non-zero temperatures is a mixed quantum state [51].

Figure 3.

Figure 3

The factor ηω,θ, Equation (29), is shown as a function of the temperature θ for ω=n/(2Γτ) with n=0(blue), n=1(green), n=2(black), n=3(orange), and n=4(red). The parameter θ0 is such a temperature when the thermal coherence length is equal to the width of the wave packet: θ0=/(πkB2Γτ).

The first effect, which leads to noise suppression, comes from the fact that each component of a mixed state is scattered independently at the wave splitter. As a result, the effect of charge quantization becomes less pronounced, and shot noise decreases with increasing temperature. At θθ0, where the characteristic temperature, θ*, is determined by the energy of an injected electron, kBθ0=/(2πΓτ), the shot noise decays as θ0/θ [61].

Suppression of a zero-frequency shot noise with temperature has been reported in [3,7,62,63]. For the source of levitons, this effect was predicted in [19].

The second effect, leading to an increase in noise, is associated with an effective broadening of the energy distribution of injected particles due to the broadening of the probability density of the components of the mixed state with increasing temperature, p(ϵ)=f1(ϵ)/ϵ, see Equation (A40). As a result, the injected particle is more likely to be able to emit energy ω in order to contribute to noise at frequency ω [9]. This increase reaches saturation at 4kBθω, which leads to the maxima in Figure 3.

4. Conclusions

The finite-frequency fluctuations of an electric current in multi-terminal conductors were analyzed at zero as well as non-zero temperatures. The focus was on the quantum coherent regime, when the current is carried by non-overlapping single-particle wave packets periodically injected into a unidirectional, chiral wave guide.

To highlight similarities and differences between auto- and cross-correlation noise, the fluctuations of an electric current were expressed in terms of the wave functions of injected electrons, bypassing the use of explicit source characteristics. Two contributions to shot noise have been identified. The first, which depends on the possible quantum exchange between the injected electrons, determines the cross-correlation noise and part of the auto-correlation noise. In the case of single-particle injection at zero temperature, this part is determined by the density profile of the injected wave packets. The second contribution, which depends on the quantum exchange of an injected electron and electrons of the Fermi sea, contributes only to the auto-correlation noise. This part is determined by the coherence of the injected wave packets multiplied by the coherence of the Fermi sea.

At zero frequency, the charge conservation tightly links both contributions to shot noise. Such a connection allows us to make some general conclusions related to the properties of excitations that can be injected/created in the Fermi sea. In particular, no excitations with a real wave function can be created in the Fermi sea without accompanying electron–hole pairs, which follows from the fact that otherwise Equation (1) would be incompatible with the conservation of charge [14]. At non-zero frequencies, the two contributions in question are generally different. They can be addressed separately by measuring both auto- and cross-correlation noise in the weak backscattering regime, R1.

For several experimentally available single-electron sources for which the wave function was calculated, I calculated and compared auto- and cross-correlation noise. For the family of so-called energy-independent sources, the source of leviton [4] is an example, the contribution related to the density profile and the contribution related to the coherence of the wave packet turn out to be the same, see Equation (5). Therefore, the auto- and cross-correlation noises are the same (up to the minus sign) at any frequency, not only at zero frequency as the charge conservation requires, see Equation (25). For another source, which relies on tunneling [42], the two contributions are manifestly different, see Equations (7) and (9) for different working regimes of the source.

I analyzed the effect of temperature on shot noise in the case when electrons are injected on top of the Fermi. It turns out that temperature affects both contributions equally, see Equation (29) for the temperature-dependent factor. As one of the contributions to shot noise depends on the quantum state of electrons in the Fermi sea, I conclude that temperature affects the quantum state of both the electrons in the Fermi sea and the injected electrons in the same way. Namely, a pure state at zero temperature becomes a mixed state at non-zero temperatures [51]. At zero frequency, changing the quantum state from pure to mixed leads to noise suppression, while at non-zero frequencies, the temperature dependence of noise is non-monotonic, see Figure 3. The temperature-dependent factor peaks when the thermal coherence time becomes of the order of the inverse of the frequency at which the noise is measured. Importantly, the position of this maximum does not depend on the properties of the sources of electrons under consideration.

Acknowledgments

I acknowledge the warm hospitality and support of Tel Aviv University. I am grateful to Pascal Degiovanni for stimulating discussions.

Appendix A. Auto-Correlation Noise from Equation (9)

After substituting Equation (8) into Equation (1), the first line, I get

Pautoexω=Re2T00dtτDtdτeiωτsinω0τπτet+τ/2τD. (A1)

To integrate with respect to t, I split the integration area into two and interchange the order of integration,

0dttdτ=0dτ0dt+0dττdt.

Then, I have

Pautoexω=Re2T0ηω,ηω=0dτcosωτeτ2τD2sinω0τπτ. (A2)

The suppression factor η(ω) is shown in Figure A1.

Figure A1.

Figure A1

A frequency-dependent suppression factor η(ω), Equation (A2). The frequency ω is given in units of ω0=Δ/(2), see Equation (8). The product ω0τD=20.

Let us first consider the case of ω=0, when

η0=0dτeτ2τD2sinω0τπτ. (A3)

The integrand in the above equation has two factors, exponentially decaying and oscillating. The wave function ψΔ, Equation (8), was calculated in the limit of ω0τD1 [35,46]. Therefore, the period of oscillations is much smaller then the time of decay. Therefore, namely, the fast oscillating factor determines an integral. The other, slowly decaying term can be calculated merely at τ=0. Thus, by using a textbook integral

0dτsinω0ττ=π2,

I arrive at η0=1.

For non-zero frequencies, I represent the factor ηω as follows:

ηω=0dτeτ2τDsinω0+ωτ+sinω0ωτπτ. (A4)

At small frequencies, ωω0, I can neglect ω compared to ω0, both sinuses becomes the same, and I recover ηωω0=η(0)=1. With this result, I reproduce Equation (9), the first line.

At ω=ω0, the second sinus nullifies, and the result is halved, ηω0=0.5. At higher frequencies, ω>ω0, the two sinuses contribute the same, but with opposite sign, and the noise gets suppressed, ηω=0. The transition from one to zero happens to occur within the region of order τD1 near ω=ω0 (that is, near ω=Δ/2) in full agreement with the previous findings [9,64]. Here, I demonstrated that the wave function ψΔ(t), Equation (8), carries information about this noise suppression effect.

The calculations leading from Equation (1), the second line to Equation (9), and the second line with the wave function from Equation (8) are rather straightforward. Importantly, the cross-correlation noise gets suppressed at much smaller frequencies of order τD1ω0.

Note that Equation (9) was calculated for the case of weak scattering into the detector, R1. In contrast, in the opposite limiting case, R=1, according to Equation (22a), the autocorrelation noise, the quantum jitter noise [8], is given by the combination of two contributions to noise. As a result, it becomes suppressed not only at large frequencies, ω>ω0, but also at small frequencies: P33ex0<ωω0|R=1=e2T0ωτD21+ωτD2.

Appendix B. Relation between an Electrical Noise and an Electron Correlation Function

Here, I generalize the results of Section 2.3 to the case when the input channels have different temperatures and Fermi energies. For this, it is convenient to separate the terms linear and bilinear in the Fermi functions f1 and f2 in Equations (14a) and (14b). I will distinguish such terms via the upper index l and b, respectively,

P33ω=e2hdEF33(E,E+ω)+P33lω+P33bω,P34ω=P34lω+P34bω. (A5)

Appendix B.1. Auto-Correlation Nose

Let us first consider P33. Substituting Equation (18) into Equations (14a) and (14b), I find

P33(ω)=e2hdE{F33(E,E+ω)+n,m,q=R2f11(Eq+ω,E)SF*(En,E)SF(Em,E)SF*(Em+ω,Eq+ω)SF(En+ω,Eq+ω)+TRf12(Eq+ω,E)δn0δm0SF*(Em+ω,Eq+ω)SF(En+ω,Eq+ω)+RTf21(Eq+ω,E)SF*(En,E)SF(Em,E)δnqδmq+T2f22(Eq+ω,E)δn0δm0δnqδmq}. (A6)

Then, I use Equation (15) and calculate a linear in Fermi functions f1 and f2 part,

P33l(ω)=e22hdERf1(E)+Rf1(E+ω)+Tf2(E)+Tf2(E+ω). (A7)

In the course of calculations, I utilized unitarity of the Floquet scattering matrix, see Equation (13). For a single-channel SF, unitarity implies the following:

n=SF*En,EmSFEn,E=δm,0,n=SF*Em,EnSFE,En=δm,0. (A8)

As an example, let us consider the very first term we need to calculate,

e22hdEn,m,q=R2f1(Eq+ω)SF*(En,E)SF(Em,E)×SF*(Em+ω,Eq+ω)SF(En+ω,Eq+ω).

To simplify it, I shift EqE under integration over energy and shift qq, nqn, mqm under the corresponding sums,

e22hdEn,m,q=R2f1(E+ω)SF*(En,Eq)SF(Em,Eq)×SF*(Em+ω,E+ω)SF(En+ω,E+ω).

Then, the sum over q gives us qSF*(En,Eq)SF(Em,Eq)=δn,m, which is used to sum over, say, m. The remaining sum over n gives nSF(En+ω,E+ω)2=1. Therefore, what left is e22h0dER2f1(E+ω). Other terms are calculated by analogy.

The bilinear in Fermi functions f1 and f2 part reads,

P33b(ω)=e2hdEn,m,q={RTf2(Eq+ω)f1(E)SF*(En,E)SF(Em,E)δnqδmq+R2f1(Eq+ω)f1(E)SF*(En,E)SF(Em,E)SF*(Em+ω,Eq+ω)SF(En+ω,Eq+ω)+TRf1(Eq+ω)f2(E)δn0δm0SF*(Em+ω,Eq+ω)SF(En+ω,Eq+ω)+T2f2(Eq+ω)f2(E)δn0δm0δnqδmq}. (A9)

Let us represent P33b(ω)=j=14Bj and calculate various terms separately. The first term is

B1=e2hdEn,m,q=R2f1(Eq+ω)f1(E)SF*(En,E)SF*(Em+ω,Eq+ω)×SF(Em,E)SF(En+ω,Eq+ω)=R2vμ2e2T0/2T0/2dtT0dτeiωτG1(1)t+τ;t2, (A10)

where G1(1) is the first-order correlation function of the Fermi sea incoming from the first channel and modified by the source, see Equation (19). To prove the last line, I compute the time integral explicitly:

0T0dtT0dτeiωτG1(1)t+τ;t2=0T0dtT0dτeiωτdEhf1EeiEτn,m=eiΩnτ×eiΩnmtSFEn,ESF*Em,EdEhf1EeiEτq,=eiΩqτeiΩqtSF*Eq,ESFE,E=

(the integration over t gives q=nm, which I use to sum up over =qn+m)

=dτeiωτdEhf1EeiEτn,m,q=eiΩnτSFEn,ESF*Em,EdEhf1EeiEτeiΩqτSF*(Eq,E)SF(Eqn+m,E).

The integration over τ gives hδωEn+Eq, which I use to integrate out En=Eq+ω,

f1(Eqn+ω)f1(E)SF*(Eq,E)SF(Eqn+m,E)×SF*(Eqn+m+ω,Eqn+ω)SF(Eq+ω,Eqn+ω).

Additionally I shift qnq,

f1(Eq+ω)f1(E)SF*(Eq+n,E)SF(Eq+m,E)×SF*Eq+m+ω,Eq+ωSFEq+n+ω,Eq+ω,

and finally, I shift q+nn and q+mm and get the same integrand as in Equation (A10) (up to EE),

f1Eq+ωf1ESF*En,ESFEm,E×SF*Em+ω,Eq+ωSFEn+ω,Eq+ω.

Other terms are calculated in the same way,

B2=e2hdEq=RTf2(Eq+ω)f1(E)SF(Eq,E)2=RTvμ2e2T0/2T0/2dtT0dτeiωτG1(1)t+τ;tG0,2(1)*τ, (A11)
B3=e2hdEq=TRf1(Eq+ω)f2(E)SF(E+ω,Eq+ω)2=TRvμ2e2T0/2T0/2dtT0dτeiωτG0,2(1)τG1(1)*t+τ;t, (A12)
B4=e2hdET2f2(E+ω)f2(E)=T2vμ2e2T0/2T0/2dtT0dτeiωτG0,2(1)τ2.1 (A13)

Putting all the terms together I get

P33bω=vμ2e20T0dtT0dτeiωτRG1(1)t+τ;t+TG0,2(1)τ2. (A14)

Note that when the second channel is also fed by a source, we need to replace the correlation function of the Fermi sea in equilibrium, G0,2(1), by the one modified by the source, G2(1).

Strictly speaking, both P33l(ω), Equation (A7), and P33b(ω), Equation (A14) diverge due to the infinite number of electrons that make up the Fermi sea, which contribute to them. However, their sum is finite. This sum is not zero even if the source is switched off. Therefore, to see the effect of injected electrons, we need to look at the excess noise. For this, I first calculate the noise when the source is off, P33off, and then calculate the excess noise as the difference, P33ex=P33P33off.

Appendix B.1.1. Equilibrium Noise, P33off

For the sake of simplicity, I assume all the reservoirs have the same Fermi energy, μα=μ,α but possibly different temperatures. If necessary, the constant bias Vα at lead α, that is, μα=μ+eVα, can be accounted for via an energy-independent scattering amplitude Sα=eieVαt.

To demonstrate that the equilibrium auto-correlation noise is not zero, I proceed as follows. I replace G1 by G0,1 in Equation (A14) for P33b, use Equation (A7) for P33l, which remains unchanged, use the following equation (see Equation (A13) and alike),

1hdEFαβ(E,E+ω)fα(E)+fβ(E+ω)2==vμ2T0/2T0/2dtT0dτeiωτG0,α(1)τG0,β(1)*τ, (A15)

and get the total equilibrium noise according to Equation (A5),

P33offω=e2hdE{F33(E,E+ω)+R2F11(E+ω,E)+TRF21(E+ω,E)+RTF12(E+ω,E)+T2F22(E+ω,E)}. (A16)

Then, I transform

Fαβ(E,E+ω)+Fβα(E,E+ω)=Fαα(E,E+ω)+Fββ(E,E+ω)+Φαβ,Φαβ=fαEfβEfαE+ωfβE+ω,

and integrate over energy using the following equations,

dEFαα(E,E+ω)=ω2cothω2kBθα,Ξθα,θβ,ω=1kBθα+θβdEΦαβ==2θαθα+θβ01dxxxΩθαθβ11xΩθαθβ111+xΩ1+xΩθαθβ1+xΩ1+xΩθαθβ, (A17)

where Ω=eω2kBθα and kB is the Boltzmann constant. Finally, I represent P33off as follows,

P33offω=e2hkB{θ3ξω2kBθ3+Rθ1ξω2kBθ1+Tθ2ξω2kBθ2+RTθ1+θ2Ξθ1,θ2,ω}, (A18)

where ξx=xcothx.

The term with factor Ξθ1,θ2,ω describes the auto-correlation thermal noise due to both terminals. It is shown in Figure A2.

Figure A2.

Figure A2

The joint two terminal contribution to the thermal noise Ξθα,θβ,ω, see Equations (A17) and (A18), is shown as a function of frequency at θα/θβ=1.1(blue), 2(green), 5(black), 10(orange), and 20(red).

Note that Ξθα,θβ,ω is zero at θα=θβ, and as a function of ω it changes a sign from positive to negative with increasing ω. This sign change occurs around ω=kBθα+θβ. At this temperature/frequency, the joint two terminal contribution to thermal noise vanishes.

Appendix B.1.2. Excess Noise, P33ex

I express the excess auto-correlation noise directly in terms of electron correlation functions Gβ and G0,β. For this I note that the electronic source affects P33b, Equation (A14), but leaves P33l, Equation (A7), unchanged. Therefore, P33ex=P33bP33b,off,

P33exω=e2vμ20T0dtT0dτeiωτ{RG0,1(1)t+τ;t+TG0,2(1)τ2RG1(1)t+τ;t+TG0,2(1)τ2}. (A19)

When both incoming channels are at the same temperature, θ1=θ2θ, and have the same Fermi energies, μ1=μ2μ, that is, their equilibrium correlation functions are the same, G0,1=G0,2G0, the above equation is simplified (see Equation (22a)).

P33exω=e2vμ20T0dtT0dτeiωτ{R2G1(1)t+τ;t22RReG1(1)t+τ;tG0(1)*τ}, (A20)

where

G1(1)t+τ;t=G1(1)t+τ;tG0,1(1)τ. (A21)

is the excess first-order correlation function injected by the source.

Appendix B.2. Cross-Correlation Nose

The cross-correlation noise in terms of G(1) was given in [51],

P34(ω)=RTe2vμ20T0dtT0dτeiωτG1(1)t+τ;tG0,2(1)τ2. (A22)

The excess cross-correlation noise, P34ex=P34P34off, reads

P34exω=RTe2vμ20T0dtT0dτeiωτ{G0,1(1)τG0,2(1)τ2G1(1)t+τ;tG0,2(1)τ2}. (A23)

If both incoming channels are under the same conditions, G0,1=G0,2G0, then, unlike the auto-correlation noise, the cross-correlation noise has no equilibrium contribution and it is expressed solely in terms of the excess correlation function G(1) (see Equation (22b)):

P34(ω)=P34ex(ω)=RTe2vμ20T0dtT0dτeiωτG1(1)t+τ;t2. (A24)

Appendix B.3. The Excess Noise Conservation at Zero Frequency

Conservation of charge imposes strong restrictions on zero frequency noise [14]. Namely, in the case under consideration, P33ex0 and P34ex0 are perfectly anti-correlated, such that

P33ex0+P34ex0=0. (A25)

To show this, let us use Equations (A19) and (A23) in the above equation and obtain

T0/2T0/2dtT0dτG1(1)t+τ;t2=0T0dtT0dτG0,1(1)τ2. (A26)

Then, I use Equations (19) and (20) and calculate the right hand side in the above equation,

r.h.s.=1hvμ2dEf12(E), (A27)

and the left hand side,

l.h.s.=1hvμ2dEn,m,qf1Eqf1ESF*En,ESFEm,ESF*Em,EqSFEn,Eq. (A28)

Using the unitarity of the Floquet scattering amplitude of the source in the above equation, see Equations (13) and (A8), I sum over n and m and get the following:

l.h.s.=1hvμ2dEf12(E)=r.h.s., (A29)

that is, Equation (A26) is proven.

Appendix B.4. Noise and the Outgoing Correlation Matrix of a Linear Electronic Circuit

To generalize equations that relate electrical noise to electron correlation functions to the case with several sources and/or with several outgoing channels, it is instructive to combine correlation functions of all incoming channels into a square matrix G^in(1), and of all outgoing channels into a square matrix G^out(1), see in [44] for details. Their dimensions are equal to the number of incoming and outgoing channels, respectively. Let us denote by S^ the scattering matrix of a stationary electronic circuit connecting incoming and outgoing channels. If S^ is independent of energy, the incoming and outgoing correlation matrix are related as follows, G^out(1)t1;t2=S^*G^in(1)t1;t2S^T, where the upper index * means complex conjugation, and T means transposition. As the incoming channels are not correlated, G^in(1) is diagonal.

In the case of a single QPC considered in this work, Gin,11(1)=G1(1), Gin,22(1)=G2(1), and two other elements are zero. The circuit’s scattering matrix is given in Equation (17), S^=S^QPC. Then, the outgoing correlation matrix reads

G^out(1)=RG1(1)+TG2(1)iRTG1(1)G2(1)iRTG2(1)G1(1)TG1(1)+RG2(1). (A30)

Comparing the elements of G^out(1) to Equations (A19) and (A23), we can relate the excess noise and the elements of the outgoing correlation matrix as follows:

Pααexω=e20T0dtT0dτeiωτvμGout,αα(1),offt+τ;t2vμGout,αα(1)t+τ;t2, (A31)

where the upper index off indicates that electronic sources are switched off.

Notice that in the above equation, the indices α and α number outgoing channels only; therefore, α,α=1,2. While in Equations (A19) and (A23), the outgoing channels were numbered together with incoming channels, thus the outgoing channels were 3 and 4, respectively. Equation (A31) is applicable for any number of electronic sources and any number of outgoing channels.

Equations (A30) and (A31) illustrate why the auto- and cross-correlation noise are generally different. In particular, there is no cross-correlation noise in equilibrium (the off-diagonal terms in Equation (A30) vanish), but autocorrelation noise is present (the diagonal terms in Equation (A30) are not zero). Ultimately, this difference is due to the fact that fermionic operators in different leads anti-commute, but do not anti-commute in one lead.

Appendix C. Noise Caused by an Electron Injected from a Quantum Level Raising at a Constant Rapidity at Zero Temperature

In this appendix, I derive Equation (28) starting from Equations (22a) and (22b).

First, I use the wave function ψ(c) from Equation (6) and calculate the excess correlation function:

G(1)t+τ;t=eiμτπΓτvμ0dxexeixt+τΓτeix2ζ0dyeyeiytΓτeiy2ζ. (A32)

Here, I introduced the parameter of non-adiabaticity ζ=τD/Γτ. This parameter controls the symmetry of the density profile of the injected wave packet [43]. With a symmetric density profile, injection is classified as adiabatic, with an asymmetric density profile, injection is non-adiabatic [46]. At ζ=0, this source is identical to the source of levitons, that is, ψc=ψL, see Equation (4) for ψL.

At the next step, let us calculate separately two terms entering Equations (22a) and (22b). I assume ΓτT0 and, therefore, extend the limits of integration over t to infinity.

Appendix C.1. The Term with vμ2G1(1)G0(1)

I denote this term as Π1. Using Equation (20) for G0(1) at zero temperature, I have

Π1(ω)=dτeiωτ2ReCτ2πiτ,Cτ=1πΓτdt0dxexeixt+τΓτeix2ζ0dyeyeiytΓτeiy2ζ, (A33)

First, I evaluate coherence Cτ. For this, I integrate over t,

dteixtΓτeiytΓτ=2πΓτδxy.

This allows us to integrate, say, over y (the result is independent of the parameter of non-adiabaticity ζ),

Cτ=20dxe2xeixΓττ=11iτ/2Γτ. (A34)

Substituting the above equation into Equation (A33), I calculate

Π1(ω)=eω2Γτ. (A35)

Note that namely this term determines the auto-correlation noise at R1: P33exωRe2/T0Π1(ω), see Equation (7).

Appendix C.2. The Term with vμ2G(1)2

I denote this term as Π2,

Π2(ω)=dtdτeiωτψ(c)t+τ2ψ(c)t2. (A36)

First, I shift τ+tτ and represent the above equation as the square of the Fourier transform of the wave packet density, Π2(ω)=Nω2, where

Nω=ΓτdzeiωΓτzψ(c)Γτz2=1πdzeiωΓτz0dxexeixzeix2ζ0dyeyeiyzeiy2ζ, (A37)

where z=τ/Γτ. The integration over z gives,

dzeiωΓτzeixzeiyz=2πδωΓτ+xy.

Then, I integrate over y=x+ωΓτ (for positive ω),

Nω=2eiωΓτ2ζeωΓτ0dxe2xei2xωΓτζ=eiωΓτ2ζeωΓτ1iωΓτζ,

and obtain (for arbitrary ω),

Π2(ω)=eω2Γτ1+ωτD2, (A38)

where τD=Γτζ. This term fully defines cross-correlation noise and partially auto-correlation noise.

Appendix C.3. Excess Noise Power

By combining both terms together, I get

P33ex(ω)=Re2T0Π1(ω)R2e2T0Π2(ω)P34(ω)=RTe2T0Π2(ω). (A39)

Using Equations (A35) and (A38) we arrive at Equation (28).

Note that at ω=0, Π1(0)=Π2(0) and P33ex(0)+P34(0)=0, in agreement with Equation (A25).

Appendix D. Noise Caused by an Electron Injected from a Quantum Level Raising at a Constant Rapidity at Non-Zero Temperature

In this appendix, I repeat the calculations presented in the previous Appendix, but at non-zero temperatures, and compute the temperature-dependent factor ηω,θ from Equation (29).

For this model, the correlation function of electrons injected at a nonzero temperature, θ>0, was expressed in terms of the correlation function at zero temperature in [60].

G1,θ(1)t+τ;t=dϵf1ϵeiϵτG1,0(1)t+τϵc;tϵc. (A40)

Here, the indices θ and 0 refer to non-zero and zero temperatures, respectively, f1 is the Fermi distribution function for electrons with temperature θ in lead 1, which the additional electron is injected into, G1,0(1) is given in Equation (A32), and the rapidity c=/2τDΓτ, see ψ(c), Equation (6).

The above equation can be interpreted as the correlation function for a single-particle mixed quantum state. Each component of this mixed state is characterized by the correlation functions eiϵτG1,0(1)t+τϵc;tϵc. The components of this mixed state are distributed according to the thermal probability density p(ϵ)=f1(ϵ)/ϵ.

Appendix D.1. The Term with vμ2G1(1)G0(1)

Using Equations (20) and (A40), I calculate

Π1(ω)=1πdτeiωτ1/τθsinhτ/τθImdϵeiϵf1ϵCτ,Cτ=dteiμτvμG1,0(1)tϵc+τ;tϵc. (A41)

As energy ϵ and time t enter G1,0(1) as a difference, tϵ/c, the correlation function calculated at zero temperature and integrated over time, Cτ, becomes independent of ϵ. This property allows us to integrate out ϵ,

Π1ω=dτeiωττ/τθsinhτ/τθ2ImCτπτ. (A42)

With G1,0(1) from Equation (A32), I calculate Cτ as described above in Appendix C.1 and find

Π1(ω)=12πΓτdτeiωττ/τθsinhτ/τθ211+τ2/2Γτ2. (A43)

Remind that the thermal coherence time τθ=/(πkBθ1). At θ1=0, we recover Equation (A35). Note that Π1(ω) obeys Equation (27).

Appendix D.2. The Term with vμ2G(1)2

At non-zero temperature the corresponding term reads

Π2(ω)=dϵdϵp(ϵ)p(ϵ)Nϵϵω2. (A44)

Here, the thermal probability density p(ϵ)=f1(ϵ)/ϵ, and

Nϵϵω=dzπeiω+ϵϵΓτz0dxexeixzϵcΓτeix2ζ0dyeyeiyzϵcΓτeiy2ζ, (A45)

where z=τ/Γτ. Up to an irrelevant phase factor, Nϵϵω is the same as Nω+ϵϵ from Equation (A37). Therefore, we can write

Π2ω=11+ωτD2dϵdϵp(ϵ)p(ϵ)eω+ϵϵ2Γτ. (A46)

To bring the above equation into the form close to Π1, Equation (A43), let us represent the exponential factor as follows,

eω+ϵϵ2Γτ=12πΓτdτeiω+ϵϵτ1+τ2/2Γτ2.

Then, we can integrate over ϵ and ϵ in Equation (A46) as follows,

dϵp(ϵ)eiϵτ=τ/τθsinhτ/τθ,

and find that

Π2ω=11+ωτD2dτeiωτ2πΓττ/τθsinhτ/τθ21+τ2/2Γτ2=Π1ω1+ωτD2, (A47)

where Π1 is given in Equation (A43).

Notice that we cannot use the inverse Fourier transformation with respect to ω in order to express Π2ω at temperature θ in terms of Π2ω at zero temperature. As a result, the excess noise, Equation (A39), does not obey Equation (27).

Appendix D.3. Excess Noise Power

The relation between Π2ω and Π1ω, Equation (A47), is independent on temperature. Therefore, the effect of temperature on Π2ω is the same as on Π1ω, see Equation (A43). Then, we use Equations (A43) and (A47) in Equation (A39) and generalize Equation (28) to the case of non-zero temperatures,

P33ex(ω)=Re2T0T+ωτD21+ωτD2eω2Γτηω,θ,P34(ω)=Re2T0T1+ωτD2eω2Γτηω,θ, (A48)

where

ηω,θ=eω2Γτdτeiωτ2πΓττ/τθsinhτ/τθ21+τ2/2Γτ2. (A49)

This factor is shown in Equation (29), where I introduced x=τ/2Γτ.

Funding

This research was funded by the Ministry of Education and Science of Ukraine, project No. 0119U002565.

Conflicts of Interest

The author declares no conflict of interest.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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