Abstract
Universal conductance fluctuations are usually observed in the form of aperiodic oscillations in the magnetoresistance of thin wires under variation of the magnetic field B. A Fourier analysis of aperiodic oscillations observed in the classical experiments by Webb and Washburn reveals a practically discrete spectrum in agreement with the scenario based on the analogy with one-dimensional systems, according to which conductance fluctuations are due to the superposition of incommensurate harmonics. A more detailed analysis reveals the existence of a continuous component, whose smallness is explained theoretically. A lot of qualitative results are obtained that confirm the presented picture: the distribution of phases, frequency differences, and the growth exponents is consistent with theoretical predictions; discrete frequencies weakly depend on the processing procedure; and the discovered shift oscillations confirm the analogy with one-dimensional systems. Microscopic estimates show that the results obtained are consistent with the geometrical dimensions of the sample.
Similar content being viewed by others
Notes
In Fig. 14 in [5], Webb and Washburn compared the Fourier spectrum of a thin wire with the spectrum of a small ring; the latter exhibits additional oscillations associated with the Aharonov–Bohm effect. In this case, aperiodic oscillations were not the subject of discussion, and their spectrum (which was of a chaotic nature due to the abrupt cutoff) was roughly approximated by the authors and represented as the envelope of oscillations. The latter was found by comparing with Figs. 12 and 13 in [5], where chaotic oscillations are shown explicitly.
Figure 1 was greatly magnified and manually digitized during processing. It turns out that the sharp spikes in the figure are associated with vertical dashes indicating experimental error, while actually the conductance is a smooth function of the magnetic field.
We emphasize that the reality of the parameters A and B is only effective. In fact, their phases turn out to be correlated, being either equal to each other or different by π. Apparently, the phases of discrete harmonics are adjusted to the specific realization of the continuous component; the mechanism of this phenomenon is not known to us and should be considered as an experimental fact.
For asymmetric lines, the processing is ambiguous due to the possibility of fitting their right or left slopes. This ambiguity was used to avoid the appearance of unphysical negative values of |F(ω)\(|_{{{\text{res}}}}^{2}\).
This can be done by heating the sample to a sufficiently high temperature.
The length L is estimated as a value of the x coordinate for which the quadratic potential m\(\omega _{B}^{2}\)x2 [9] is compared with the Fermi energy \({{\epsilon }_{F}}\), so that L ∝ B–1. However, if the energy \({{\epsilon }_{F}}\) is comparable to the first Landau level, then it must be replaced by \(\hbar \)ωB = \(\hbar \)eB/mc, which gives the dependence L ∝ B–1/2. As is clear from Section 10, near the middle of the experimental range of magnetic fields, the second estimate is more adequate.
This extrapolation is complicated by factors that shift the origin of L (see Section 5 in [8]).
The effective linearity of the extrapolation is due to the fact that the main contribution to F(ω) comes from the middle of the experimental range of fields (see Section 5), where the relationship between L and B is practically linear.
The exponents αs change sign when passing from the magnetic field B to the effective length of the system L (the right and left directions interchange). When passing from conductance to resistance, there is no change in the signs of αs, since small fluctuations of these two quantities are proportional to each other.
Here the difference between the real system and the Anderson model considered in [8] is essential. In the Anderson model, the metallic regime corresponds to a high concentration of weak impurities, which can be considered by perturbation theory. In a real system, weak disorder is created by low concentration of strong impurities, for which the slow particle approximation is valid. This difference does not affect the results for the exponents, since, on the wavelength scale, the configuration of the random potential can be varied within wide limits without affecting the large-scale properties of the wave functions.
Equation (19) has the same form if we set L = L0 + l or L = L0 – l and consider the evolution with respect to l. This is clear from the scheme for deriving similar equations (see Appendix A in [41]).
In this case, the roots x1, x2, x3 should be expanded in \({{\epsilon }^{2}}\)/δ to the higher order than in [8].
It is easy to verify that the Fourier transforms of the functions f(x)G(x + a) and f(x)G(x – a) have the same real parts but opposite imaginary parts.
REFERENCES
B. L. Al’tshuler, JETP Lett. 41, 648 (1985).
B. L. Al’tshuler and D. E. Khmel’nitskii, JETP Lett. 42, 359 (1985).
P. A. Lee and A. D. Stone, Phys. Rev. Lett. 55, 1622 (1985).
P. A. Lee, A. D. Stone, and Y. Fukuyama, Phys. Rev. B 35, 1039 (1987).
S. Washburn and R. A. Webb, Adv. Phys. 35, 375 (1986).
Mesoscopic Phenomena in Solids, Ed. by B. L. Altshuler, P. A. Lee, and R. A. Webb (North-Holland, Amsterdam, 1991).
C. W. J. Beenakker, Rev. Mod. Phys. 69, 731 (1997).
I. M. Suslov, J. Exp. Theor. Phys. 129, 877 (2019).
L. D. Landau and E. M. Lifshitz, Course of Theoretical Physics, Vol. 3: Quantum Mechanics: Non-Relativistic Theory (Nauka, Moscow, 1975; Pergamon, New York, 1977).
D. Mailly and M. Sanquer, J. Phys. I 2, 357 (1992).
V. V. Brazhkin and I. M. Suslov, J. Phys.: Condensed Matter (accepted); arXiv: 1911.10441.
W. H. Press, B. P. Flannery, S. A. Teukolsky, and W. T. Wetterling, Numerical Recipes in Fortran (Cambridge Univ. Press, Cambridge, 1992).
A. B. Migdal, Qualitative Methods in Quantum Theory (Nauka, Moscow, 1975; Addison-Wesley, Reading, MA, 1989).
V. I. Mel’nikov, Sov. Phys. Solid State 23, 444 (1981).
A. A. Abrikosov, Solid State Commun. 37, 997 (1981).
N. Kumar, Phys. Rev. B 31, 5513 (1985).
B. Shapiro, Phys. Rev. B 34, 4394 (1986).
P. Mello, Phys. Rev. B 35, 1082 (1987).
B. Shapiro, Philos. Mag. 56, 1031 (1987).
K. M. D. Hals, A. K. Nguyen, X. Waintal, and A. Brataas, Phys. Rev. Lett. 105, 207204 (2010).
A. S. Lien, L. Y. Wang, C. S. Chu, and J. J. Lin, Phys. Rev. B 84, 155432 (2011).
J. G. G. S. Ramos, D. Bazeia, M. S. Hussein, and C. H. Lewenkopf, Phys. Rev. Lett. 107, 176807 (2011).
Z. Li, T. Chen, H. Pan, et al., Sci. Rep. 2, 595 (2012).
E. Rossi, J. H. Bardarson, M. S. Fuhrer, and S. D. Sarma, Phys. Rev. Lett. 109, 096801 (2012).
P. Y. Yang, L. Y. Wang, Y. W. Hsu, and J. J. Lin, Phys. Rev. B 85, 085423 (2012).
S. Minke, J. Bundesmann, D. Weiss, and J. Eroms, Phys. Rev. B 86, 155403 (2012).
S. Gustavsson, J. Bylander, and W. D. Oliver, Phys. Rev. Lett. 110, 016603 (2013).
A. L. R. Barbosa, M. S. Hussein, and J. G. G. S. Ramos, Phys. Rev. E 88, 010901(R) (2013).
Ph. Jacquod and I. Adagideli, Phys. Rev. B 88, 041305(R) (2013).
J. Bundesmann, M. H. Liu, I. Adagideli, and K. Richter, Phys. Rev. B 88, 195406 (2013).
C. L. Richardson, S. D. Edkins, G. R. Berdiyorov, et al., Phys. Rev. B 91, 245418 (2015).
T. C. Vasconcelos, J. G. G. S. Ramos, and A. L. R. Barbosa, Phys. Rev. B 93, 115120 (2016).
C. C. Kalmbach, F. J. Ahlers, J. Schurr, et al., Phys. Rev. B 94, 205430 (2016).
J. G. G. S. Ramos, A. L. R. Barbosa, B. V. Carlson, et al., Phys. Rev. E 93, 012210 (2016).
Y. Hu, H. Liu, H. Jiang, and X. C. Xie, Phys. Rev. B 96, 134201 (2017).
H. C. Hsu, I. Kleftogiannis, G. Y. Guo, and V. A. Gopar, J. Phys. Soc. Jpn. 87, 034701 (2018).
M. A. Aamir, P. Karnatak, A. Jayaraman, et al., Phys. Rev. Lett. 121, 136806 (2018).
S. Islam, S. Bhattacharyya, H. Nhalil, et al., Phys. Rev. B 97, 241412R (2018).
T. Vercosa, Y. J. Doh, J. G. G. S. Ramos, and A. L. R. Barbosa, Phys. Rev. B 98, 155407 (2018).
F. Hajiloo, F. Hassler, and J. Splettstoesser, Phys. Rev. B 99, 235422 (2019).
I. M. Suslov, J. Exp. Theor. Phys. 124, 763 (2017).
ACKNOWLEDGMENTS
The author is grateful to V.V. Brazhkin, who initiated the work [11].
Author information
Authors and Affiliations
Corresponding author
Additional information
Translated by I. Nikitin
Appendices
APPENDIX A
1.1 Solution of Equation (19)
We restrict the analysis to the metallic region when typical values of ρ are small. Considering the eigenvalue problem for the operator on the right-hand side of Eq. (19) and restricting ourselves to the lowest order in ρ, we have the equation
Assuming that ρ varies in the range from zero to R, we impose the finiteness condition at ρ = 0 and the zero boundary condition at ρ = R. Then the eigenvalues and eigenfunctions have the form
where μs are the roots of the Bessel function J0(x). Solving Eq. (19) with the initial condition (22) by expanding P(ρ) in terms of eigenfunctions (A.2), we have
where t = α(L – L0) and it is taken into account that, for large R, the spectrum of the eigenvalues μs becomes quasicontinuous and the summation over s can be replaced by integration with respect to μ using the asymptotics μs = πs + const for large s. Calculating the integral in (A.3), we obtain
where I0(x) = J0(ix). For ρ \( \lesssim \) t and t ≫ ρ0, distribution (A.4) transforms into (21), and, for ρ ≈ ρ0 and t ≪ ρ0, it becomes Gaussian,
The closeness of (A.4) to the Gaussian distribution allows us to characterize it by the first two moments. Multiplying (19) by ρn and integrating with respect to ρ, we obtain evolution equations for the moments of the distribution P(ρ); their solution for the initial condition (22) has the form
For small ρ, the expressions are simplified,
and correspond to distribution (A.4). These results are valid for L > L0. The description of evolution in the range 0 < L < L0 is complicated by the need to satisfy two conditions (20) and (22), which is possible only under certain restrictions on the realization of the random potential. These restrictions are imposed on the interval (0, L0) as a whole and are not significant for small L and L close to L0. In the first case, we have 〈ρ〉 = σ in accordance with distribution (21). In the second case, the situation is determined by the fact that the broadening of the distribution occurs symmetrically when L deviates to the right or left of L0.Footnote 11 For the quantity 〈ρ〉, conditions (20) and (22) are automatically satisfied if ρ0 is chosen equal to the mean value of distribution (21) for L = L0. As a result of the aforesaid, we arrive at the picture shown in Fig. 8.
APPENDIX B
1.1 Evolution of 〈ρ〉 for the Initial Condition (22)
The calculation of 〈ρ〉 technically reduces to studying the evolution of the second moments for the transfer matrix with complex elements Tij [8]:
They satisfy the system of difference equations, whose general solution has the form [8]
where x1, x2, and x3 are the roots of the first equation in (37) and
Here α = –Δ2δ, Δ = Δ1δ, and δ and \({{\epsilon }^{2}}\) were defined after (23),
where \(\bar {k}\) and k are the Fermi momenta in the system under study and the ideal leads connected to it. In contrast to [8], as the initial condition, we take the general transfer matrix
with ρ = ρ0 and ψ = θ – φ, rather than the identity matrix. The quantity \(z_{4}^{{(n)}}\) immediately determines 〈ρ〉, giving a general expression for the latter:
where
and
Using the asymptotics for the roots x1, x2, and x3 in the metallic regime [8], we arrive at the results (23) and (25). The first of them is valid for “natural” ideal leads,Footnote 12 which differ from the studied system only by the absence of the random potential in them; in this case, k = \(\bar {k}\), Δ1 = 0, and the oscillations appear in the first order in the small parameter \({{\epsilon }^{2}}\)/δ. The result (25) is valid for foreign leads when Δ1 ≠ 0 and oscillations occur in the zero order in \({{\epsilon }^{2}}\)/δ. Using the asymptotics of x1, x2, and x3 in the “critical” region [8] leads to the result (24), which is valid near the edge of the initial band; it is given for “natural” leads, since the situation for foreign leads is sufficiently characterized by the formulas given in [8].
APPENDIX C
1.1 On the Choice of the Natural Origin
According to the Onsager relations, conductance is an even function of the magnetic field B, and, when x = B, the function f(x) in (3) is even. Let us choose a smoothing function in the form G(x – a) + G(x + a) with even G(x), i.e., in a form symmetrized with respect to x. Then the Fourier transform is real and coincides, up to sign, with its modulus; therefore, it does not contain shift oscillations. Now we eliminate the function G(x + a). The resulting Fourier transform F(ω) of the function f(x)G(x – a) is complex; its real part is half the previous one and does not contain shift oscillations.Footnote 13 The latter are also absent in ImF(ω), since they equally affect the real and imaginary parts. After the shift x → x + a, the Fourier transform takes the form
and the resulting integral for a = μ0 corresponds to that considered in Section 2, while the factor eiωa corresponds to the shift oscillations. However, the sign of a obtained in this case does not correspond to that found empirically.
The reason for the contradiction is that the Onsager symmetry distinguishes not only the value B = 0, but also B = ∞; it is the latter value that corresponds to the empirical situation. When choosing x = 1/B, we can repeat all the previous arguments; however, the increments of B and x have opposite signs, and, for a qualitative agreement with Section 2, we should change the sign of ω. This will give rise to a factor eiωa with the correct sign of a.
Rights and permissions
About this article
Cite this article
Suslov, I.M. Spectral Analysis of Universal Conductance Fluctuations. J. Exp. Theor. Phys. 131, 793–808 (2020). https://doi.org/10.1134/S1063776120100155
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1063776120100155