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The Interaction of Electrons and Lattice Vibrations

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Solid-State Physics

Abstract

The concept of the “particle” as an entity by itself makes sense only if its life time in a given state is fairly long even with the interactions.

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Notes

  1. 1.

    A simplified approach to these ideas is in Patterson [4.33]. See also Mattuck [17, Chap. 1].

  2. 2.

    Things may be a little more complicated, however, as the distinction between normal and umklapp may depend on the choice of primitive unit cell in k space [21, p. 502].

  3. 3.

    This may not be true when electrons are scattered by polar optical modes.

  4. 4.

    See McMillan and Rowell [4.29].

  5. 5.

    See, E.G., [4.26]. Note also that a ‘Fermi Polaron’ Has Been Created by Putting a Spindown Atom in a Fermi Sea of Spin-up Ultra-Cold Atoms. See Frédéric Chevy, “Swimming in the Fermi Sea,” Physics 2, 48 (2009) Online. This Research Deepens the Understanding of Quasiparticles.

  6. 6.

    See Mott [4.31].

  7. 7.

    See [4.19]. See also Sect. 9.5.3.

  8. 8.

    See Langer and Vosko [4.24].

  9. 9.

    See also Sect. 12.8.3 where the half-integral quantum Hall effect is discussed.

  10. 10.

    See Table 4.5 for a more precise statement about what is held constant.

  11. 11.

    For a discussion of how to treat such cases, see, for example, Howarth and Sondheimer [4.13].

  12. 12.

    As emphasized by Arajs [4.3], (4.146) should not be applied blindly with the expectation of good results in all metals (particularly for low temperature).

  13. 13.

    Equation (4.149) is the same as (4.138) and (4.145) with \( {\boldsymbol{\nabla}}\mu = 0 \) and B \( = \) 0. These are typical conditions for metals, although not necessarily for semiconductors.

  14. 14.

    This is basically Maxwell–Garnett theory. See Garnett [4.9]. See also Reynolds and Hough [4.36].

  15. 15.

    See Stratton [4.38].

  16. 16.

    See Bergmann [4.4].

  17. 17.

    Also of some interest is the variation in K due to inaccuracies in the input parameters (such as K1, K2) for different models used for calculating K for a composite. See, e.g., Patterson [4.34].

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Correspondence to James D. Patterson .

Problems

Problems

  1. 4.1

    According to the equation

$$ K = \frac{1}{3}\sum\limits_{m} {C_{m} \bar{V}_{m} \lambda_{m} ,} $$

the specific heat Cm can play an important role in determining the thermal conductivity K. (The sum over m means a sum over the modes m carrying the energy.) The total specific heat of a metal at low temperature can be represented by the equation

$$ C_{v} = AT^{3} + BT, $$

where A and B are constants. Explain where the two terms come from.

  1. 4.2

    Look at Figs. 4.7 and 4.9 for the thermal conductivity of metals and insulators. Match the temperature dependences with the “explanations.” For (3) and (6) you will have to decide which figure works for an explanation.

(1) T:

(a) Boundary scattering of phonons \( {\text{K}} = C\bar{V}\lambda /3 \), and \( \bar{V},\lambda \) approximately constant

(2) T2:

(b) Electron–phonon interactions at low temperature changes cold to hot electrons and vice versa

(3) constant:

(c) CvT

(4) T3:

(d) T > θD, you know ρ from Bloch (see Problem 4.4), and use the Wiedemann–Franz law

(5) Tneβ/T:

(e) C and \( \bar{V} \cong {\text{ constant}} \). The mean squared displacement of the ions is proportional to T and is also inversely proportional to the mean free path of phonons. This is high-temperature umklapp

(6) T−1:

(f) Umklapp processes at not too high temperatures

  1. 4.3

    Calculate the thermal conductivity of a good metal at high temperature using the Boltzmann equation and the relaxation-time approximation. Combine your result with (4.160) to derive the law of Wiedemann and Franz.

  2. 4.4

    From Bloch’s result (4.146) show that σ is proportional to T−1 at high temperatures and that σ is proportional to T−5 at low temperatures. Many solids show a constant residual resistivity at low temperatures (Matthiessen’s rule). Can you suggest a reason for this?

  3. 4.5

    Feynman [4.7, p. 226], while discussing the polaron, evaluates the integral

$$ I = \int {\frac{{{\text{d}}\varvec{q}}}{{q^{2} f\left( \varvec{q} \right)}},} $$

[compare (4.112)] where

$$ d\varvec{q} = {\text{d}}q_{x} \;{\text{d}}q_{y} \;{\text{d}}q_{z} , $$

and

$$ f\left( \varvec{q} \right) = \frac{{\hbar^{2} }}{2m}\left( {2\varvec{k} \cdot \varvec{q} - q^{2} } \right) - \hbar \omega_{\text{L}} , $$

by using the identity:

$$ \frac{1}{{K_{1} K_{2} }} = \int\limits_{0}^{1} {\frac{{{\text{d}}x}}{{[K_{1} x + K_{2} \left( {1 - x} \right)^{2} ]}}} . $$
  1. a.

    Prove this identity

  2. b.

    Then show the integral is proportional to

    $$ \frac{1}{k}\sin^{ - 1} \frac{{K_{3} k}}{\sqrt 2 }, $$

    and evaluate K3.

  3. c.

    Finally, show the desired result:

$$ E_{{\varvec{k},0}} = - \alpha_{\text{c}} \hbar \omega_{\text{L}} + \frac{{\hbar^{2} k^{2} }}{{2m^{ * * } }}, $$

where

$$ m^{ * * } = \frac{{m^{ * } }}{{1 - \frac{{\alpha_{c} }}{6}}}, $$

and m* is the ordinary effective mass.

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Patterson, J.D., Bailey, B.C. (2018). The Interaction of Electrons and Lattice Vibrations. In: Solid-State Physics. Springer, Cham. https://doi.org/10.1007/978-3-319-75322-5_4

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