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Pr1-1 (cid:13)c 6 0 0 2 n a J 1 Coulombian disorder in Charge Density Waves 1 ] Alberto Rosso1, Edmond Orignac2, R. Chitra3 and Thierry Giamarchi4 n n 1 Laboratoire de physique th´eorique et mod`eles statistiques CNRS UMR8626 - s Baˆt. 100 Universit´e Paris-Sud; 91405 Orsay Cedex, France; e-mail: [email protected] i d 2 Laboratoire de physique th´eorique de l’E´cole Normale Sup´erieure, . CNRSUMR8549,24,RueLhomond,75231ParisCedex05,France;e-mail: [email protected] t a 3 Laboratoire de physique th´eorique de la mati`ere condens´ee CNRS UMR7600 m Universit´e de Pierre et Marie Curie, 4, Place Jussieu 75252 Paris Cedex 05 France; e-mail: - [email protected] d n 4 Universit´e de Gen`eve, DPMC, 24 Quai Ernest Ansermet, CH-1211 Gen`eve 4, Switzerland; o e-mail: [email protected] c [ 1 v Abstract 9 3 When unscreened charged impurities are introduced in charge density wave system the 2 1 longwavelengthcomponentofthedisorderislongrangedanddominatesstaticcorrelation 0 functions. Wecalculatethex-rayintensityandfindthatitisidenticaltotheoneproduced 6 by thermal fluctuationsin a disorder-free smectic-A. Wesuggest that thiseffect could be 0 observed in the blue bronze material K0.3MoO3 doped with charged impurities such as / Vanadium. t a m - d 1 INTRODUCTION n o c Quasi-onedimensionalmaterialformedofweaklycoupledchainsareknowntoposseslowtem- : peratureinstabilitytowardsastatewithanincommensuratestaticmodulationoftheelectronic v charge and of the lattice displacement known as charge density wave (CDW) phase. CDWs i X behaveaselastic systems[1,2]providedCoulombinteractionarescreened. WhenCoulombin- r teraction are not sufficiently screened elasticity becomes non-local [3,4] and disorder becomes a long ranged correlated. An important question is whether the competition of the non-local elasticitywiththe long-rangerandompotentialresultsinthe completedestructionofthe crys- tallineorder,orwhethersomeremnantsoftheunderlyingperiodicstructureremainobservable. Apowerfulexperimentaltechnique abletocharacterizethestructuralpropertiesofCDWwith impurities is affordedby x-raydiffraction. Inthis paper we derivethe static displacementcor- relationfunctionsandx-rayintensityoftheCDWwithchargedimpuritiesandwehighlightthe similitude of the latter to the x-ray intensity of smectic-A liquid crystals subjected to thermal fluctuations. Finally, we discuss the experimental significance of our result and suggest that the smectic-like correlations should be observable in experiments on KMo1−xVxO3. 1-2 2 CHARGE DENSITY WAVE WITH CHARGED IMPURITIES We consider an incommensurate CDW, in which the electron density is modulated by a wave vectorQincommensuratewiththeunderlyingcrystallattice. Inthisphase,theelectrondensity has the following form [1,2]: ρ ρ(r)=ρ + 0Q φ(r)+ρ cos(Q r+φ(r))), (2.1) 0 Q2 ·∇ 1 · whereρ ,istheaverageelectronicdensity. ThesecondterminEq.(2.1)isthelongwavelength 0 density and corresponds to variations of the density over scales larger than Q−1 . The last oscillating term describes the sinusoidal deformation of the density at a scale of the order of Q−1 induced by the formation of the CDW with amplitude ρ and phase φ. 1 The low energy properties of the CDW are described by an elastic Hamiltonian for the fluctuations of the phase φ. When the Coulomb interactions are unscreened this Hamilto- nian becomes non-local. Choosing the x axis aligned with Q the total Hamiltonian in three dimensions reads [3,4]: 1 H = H +H = G−1(q)φ(q)2, (2.2) el. 0 C 2 | | Z n ¯hv v2 q2 G−1(q) = c F ⊥ x +q2 2πv2 q2ξ2 ⊥ x (cid:20) 0 (cid:21) where v is the Fermi velocity and n is the number of chains per unit surface that crosses F c a plane orthogonal to Q. The velocity of the phason excitations parallel to Q is v = x (me/m∗)1/2vF with m∗ the effective mass of the CDW and me the mass of an electron. v⊥ denote the phason velocities in the transverse directions. The lengthscale ξ is defined by: 0 n ¯hv v2 ξ2 = c F ⊥Q2ǫ. (2.3) 0 2πv2e2ρ2 x 0 where wehaveassumedforsimplicity anisotropicdielectric permittivity ǫ ofthe hostmedium and e is the charge of the electron. When a non-zero concentration of charged impurities is present, the Hamiltonian becomes: e2 ρ (r)ρ(r′) H = H + d3rd3r′ imp. , el. 4πǫ r r′ Z | − | (2.4) where ρ (r) is the density of impurities at position r. We assume Gaussian distributed imp impuritieswithρ (r)ρ (r’)=Dδ(r r’),whereD isthemeasureofthedisorderstrength. imp imp − Using the expressionofthe density in (2.1), the interactionwith disordercomprises twoparts, one that describes the interaction with long wavelength fluctuations of the density (forward scattering),andasecondpartthatdescribesinteractionsofimpuritieswithdensityfluctuations of wavelength Q−1 (backward scattering). In [5] we have shown that even in the case of long rangedisorder,thebackwardscatteringtermsbehaveessentiallyliketheirshortranged(neutral impurities) counterparts. In that case, it is known that in three dimensions, the contribution of the backward scattering to the phase correlations grows slowly as log(logr). [6,7] The contribution of the forward scattering term is obtained from the Hamiltonian: d3q G−1(q) iρ e2q H = φ(q)2+ 0 xρ ( q)φ(q) , (2π)3 2 | | Qǫq2 imp. − Z (cid:20) (cid:21) (2.5) Pr1-3 and reads in the limit of r⊥,x : →∞ B(r) = (φ(r) φ(0))2 h − i r2 +4xξ ⊥ 0 = κln | | . (2.6) Λ−2 (cid:18) ⊥ (cid:19) where Λ⊥ is a momentum cutoff and: DQ2 DQev 1 x κ= = . (2.7) 16πξ0ρ20 8ρ0v⊥ √nchvFǫ As a result, in the presence of charged impurities, the forward scattering terms generate the leading contribution to the phase correlations. 3 X-RAY SPECTRUM AND ANALOGY WITH SMECTICS A Itis wellknownthatthe presence ofa CDWin acompoundis associatedwith the appearance of two satellites at positions q K Q around each Bragg peak. [8] The intensity profiles ∼ ± of these satellites give access to the structural properties of the CDW. The main contribution to the x-ray satellite intensity is given by I , which is symmetric under inversion around the d Bragg vector K. [7,9–12] The intensity I is given by the following correlation function: d I (K+Q+k) = u2f2K2 d3re−ik·rC (r), d 0 d Z C (r) = ei(φ(r/2)−φ(−r/2)) (3.1) d D E where f is an averagex-rayscattering amplitude and u is the amplitude of the lattice modu- 0 lation induced by the presence of the CDW. Using the result given in Eq.(2.6) we extract the small k behavior of the intensity peak: (k )κ−2 for k2ξ k , I (K+Q+k) | x| ⊥ 0 ≪| x| (3.2) d ∼((k⊥ )2(κ−2) otherwise. | | The intensity I (K+Q+k) is divergent for κ < 2 but is finite for κ > 2, i.e. for strong d disorder. We note that these intensities are remarkably similar to those of a disorder-free smectic-A liquid crystal [13] at positive temperature. In fact, the expression of the exponent κ Eq. (2.7) is analogousto the expression(5.3.12)in [14],with the disorderstrength D playing the role of the temperature T in the smectic-A liquid crystal. Let us turn to an estimate of the exponent κ appearing in the intensities to determine whether such smectic-like intensities are indeed observable in experiments. A good candidate is the blue bronze material K MoO which has a full gap so that Coulomb interactions are 0.3 3 unscreened at low temperature. We use the parameters of [15]: n =1020chains/m2, (3.3) c v =1.3 105m.s−1, (3.4) F × ρ =3 1027e−/m3, (3.5) 0 × Q=6 109m−1, (3.6) × 1-4 and a relative permittivity of ǫ = 1, so that ǫ is equal to the permittivity of the K0.3MoO3 vacuum. For the doped material K0.3Mo1−xVxO3, we find that the disorder strength can be expressed as a function of the doping and obtain: #(Mo atoms/unit cell) D =x(1 x) . (3.7) − a (b c) · × Forthecrystalparameters,a=18.25˚A,b=7.56˚A,c=9.86˚A,β =117.53o[16],with20Molybde- numatomsperunitcell,andadopingx=3%,thedisorderstrengthD =4.8 1026m−3. More- over, using the experimental bounds of the velocities: 3.6 102m.s−1 <v⊥×<1.6 103m.s−1 andv =3.7 103m.s−1,wefindthatκisintherange[0.1×6 0.8]. Therefore,the×smectic-like x × − order should be observable in x-ray diffraction measurements on this material. References [1] G.Gru¨ner, DensityWaves inSolids, Addison-Wesley,Reading,MA,1994. [2] S.BrazovskiiandT.Nattermann, Adv.Phys.53,177(2004). [3] K.B.EfetovandA.I.Larkin, Sov.Phys.JETP45,1236(1977). [4] P.A.LeeandH.Fukuyama, Phys.Rev.B17,542(1978). [5] E.Orignac,A.Rosso,R.Chitra,andT.Giamarchi, Phys.Rev.B73,035112 (2006). [6] R.Chitra,T.Giamarchi,andP.L.Doussal, Phys.Rev.B59,4058(1999). [7] A.RossoandT.Giamarchi, Phys.Rev.B70,224204(2004). [8] J.M.Cowley, Surf.Sci.298,336(1993). [9] S.Ravy,J.-P.Pouget, andR.Com`es, J.dePhys.I2,1173(1992). [10] S.Brazovskii,J.-P.Pouget, S.Ravy,andS.Rouzi`ere, Phys.Rev.B55,3426(1997). [11] S.Rouzi`ere,S.Ravy,J.P.Pouget, andS.Brazovskii, Phys.Rev.B62,R16231(2000). [12] A.RossoandT.Giamarchi, Phys.Rev.B68,140201(R) (2003). [13] A.Caille, C.R.Acad.Sci.Ser.B274,891(1972). [14] S.Chandrasekhar, Liquidcrystals,chapter5,page312, CambridgeUniversityPress,Cambridge,UK,2nd edition,1992. [15] J. P. Pouget, in Low–Dimensional Electronic Properties of Molybdenum Bronzes and Oxides, edited by C.Schlenker, page87,Kluwer,Dordrecht,1989. [16] M.Sato,H.Fujishita,S.Sato,andS.Hoshino, J.Phys.C18,2603(1985).

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