Eigenstate Thermalization Hypothesis in Conformal Field Theory

Total Page:16

File Type:pdf, Size:1020Kb

Eigenstate Thermalization Hypothesis in Conformal Field Theory Eigenstate thermalization hypothesis in conformal field theory The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. Citation Lashkari, Nima et al. “Eigenstate Thermalization Hypothesis in Conformal Field Theory.” Journal of Statistical Mechanics: Theory and Experiment 2018, 3 (March 2018): 033101 © 2018 IOP Publishing Ltd and SISSA Medialab srl As Published http://dx.doi.org/10.1088/1742-5468/aab020 Publisher IOP Publishing Version Original manuscript Citable link http://hdl.handle.net/1721.1/120293 Terms of Use Creative Commons Attribution-Noncommercial-Share Alike Detailed Terms http://creativecommons.org/licenses/by-nc-sa/4.0/ Eigenstate Thermalization Hypothesis in Conformal Field Theory Nima Lashkari,1 Anatoly Dymarsky,2 and Hong Liu1 1Center for Theoretical Physics, Massachusetts Institute of Technology, Cambridge, MA 02139 2Department of Physics and Astronomy, University of Kentucky, Lexington, KY 40506, USA Skolkovo Institute of Science and Technology, Skolkovo Innovation Center, Moscow 143026 Russia We investigate the eigenstate thermalization hypothesis (ETH) in d+1 dimensional conformal field theories by studying reduced density matrices in energy eigenstates. We show that if local probes of high energy primary eigenstates satisfy ETH, then any finite energy observable with support on a subsystem of finite size satisfies ETH. In two dimensions, we discover that if ETH holds locally, the finite size reduced density matrix of states created by heavy primary operators is well-approximated by a projection to the Virasoro identity block. INTRODUCTION proving local ETH should amount to understanding how the corresponding statement regarding OPE coefficients Whether and how an isolated interacting quantum sys- connects with non-integrability. tem initially out of equilibrium equilibrates is a complex We believe that local ETH provides a powerful techni- dynamical question about which we currently have little cal handle for obtaining many dynamical properties of a analytic control. For a non-integrable system, there is CFT. As a simple application we use it to compute the nevertheless a powerful conjecture{the Eigenstate Ther- Renyi entropies for an interval in an energy eigenstate malization Hypothesis (ETH){which states that expecta- in a (1+1)-dimensional CFT. Interestingly we find that tion values of generic few-body observables in a finitely even though the reduced density matrix for the region excited energy eigenstate should coincide with those in approaches that of the canonical ensemble in the ther- the micro-canonical ensemble up to corrections that are modynamic limit, the Renyi entropies differ by a finite exponentially small in entropy [1, 2]. Assuming ETH, amount. one can then readily deduce that in the thermodynamic Our discussion should be generalizable to general quan- limit: (i) expectation values of few-body observables in tum field theories which we will pursue elsewhere. a generic state coincide with those in a thermal ensem- ble; (ii) expectation values of few-body observables in a SETUP non-equilibrium initial state will evolve towards those of a thermal ensemble. Consider finitely excited energy eigenstate E of a con- By now, there are many numerical evidences for ETH formal field theory in a d-dimensional spacej ofi finite vol- in a variety of quantum systems [3]. While ETH was ume. For simplicity, we take it to be a sphere of radius L often stated for few-body observables, recently numeri- (i.e. the total spacetime is Sd). A key simplification cal supports were also found for the full reduced density Rt of conformal symmetry is that× in Euclidean signature any matrix of any subsystem [4, 5]. state on Sd can be mapped through conformal trans- ETH is powerful as instead of following time evolu- formationj i tion of a general non-equilibrium state, we now face an in-principle simpler problem of understanding properties 2 2 2 2 2 2 2 2 dscylinder = dτ + L dΩd = Λ (dr + r dΩd) of finitely excited energy eigenstates. Unfortunately, de- L spite much numerical progress energy eigenstates of a Λ = ; τ = L log r (1) arXiv:1610.00302v1 [hep-th] 2 Oct 2016 r general interacting many-body system are still too com- plex to be tractable by analytic methods. A proof of to a local operator Ψ inserted at origin (r = 0) in Rd+1. ETH for general non-integrable systems appears out of Similarly, the conjugate state is mapped to a local h j d+1 reach at this stage. operator Ψy inserted at r = in R . Energy eigen- 1 In this paper we show that progress can be made in states are in one-to-one correspondence to the operators conformal field theories (CFT). We are able to prove that P P Ψ , where P is a momentum operator and µ1 ··· µm a µ for CFTs, a weakest form ETH which applies to local pri- Ψa is a primary operator. Below, we will use state and mary operators (to which we refer as local ETH) in fact operator languages interchangeably. leads to a strongest form of ETH which applies to the Kinematics of conformal symmetry fixes the corre- reduced density matrix of a general subsystem. Thus to lators in descendant states P P Ψ , in terms of µ1 ··· µm a prove ETH for CFTs it is enough to prove that it applies those of their corresponding primary Ψa. The dynam- to local primary operators which in turn reduces to a ical content of a CFT is the spectrum of its primaries statement regarding coefficients in operator product ex- and OPE coefficients. As a dynamical statement about pansions (OPE). Clearly not all CFTs satisfy ETH, thus energy eigenstates which are not related by symme- 2 tries ETH should be restricted to primary energy eigen- 2. Introducing σab TrBc Ea Eb , then states. Moreover, we will restrict our attention to ho- ≡ j ih j iα iα O(S(E)) mogeneous energy eigenstates on Sd which are invariant e σab + e− σba e− : (6) k k ∼ under SO(d + 1) rotations. Such an energy eigenstate for all α. with energy Ea corresponds to a spinless primary Ψa of dimension ha = Ea=L. The energy density of the sys- Note that subsystem ETH (5){(6) implies local ETH, Ea ha tem is a = d = d+1 , where !d is the volume of a L !d L d that is, for an operator supported inside region B we d unit S . For a CFT in a thermal state of temperature T , have O d+1 a CT where C is central charge, which motivates ∼ a a 1 a 2 1 us to define a \thermal" length scale associated with Ea Tr((ρ ρ (E) ) ρ ρ (E) 2 Tr((ρ +ρ (E)) ) 2 j i B− B O ≤ k B− B k B B O 1 (7) a − d+1 1 and thus is exponentially small. Similarly, Tr( σ ) = λT = T − : (2) ab O(S(E)) O C ∼ e− . See supplementary material for a proof 2 We will be interested in the thermodynamic limit with of (7). To close our setup, let us briefly comment on the de- L , while keeping a finite energy density a and thus a finite! 1λ . In this limit the scaling dimension h should scendant eigenstates. As an example consider E corre- T a 2 l j i then scale with L as sponding to a spinless operator (Pµ ) Ψa where l an inte- 2l ger. For such a state E = Ea;l = Ea + . The matrix ele- d+1 L L ment E p E is controlled by that in the primary state ha = C!d : (3) h jO j i λ Ψ , i.e. by O (E 2l ) rather than O (E). Thus as stated T a p L p earlier, we should− not include the descendant states in The local ETH condition is defined as either (4) or (5){(6). Of course if one assumes (4), for 2l p ha l, from smoothness of function Op(E), Op(E L ) Ea p Eb = Op(E)δab + Oab; (4) − h jO j i is related to Op(E) only by corrections of order l=ha and similarly the corresponding reduced density matrix where p is a local primary operator (with p labeling O is close to ρB(E) in trace distance with corrections that different operators), the diagonal element Op(E) is a Ea+Eb p O(S(E)) are polynomially suppressed in l=ha. But such state- smooth function of E = , and O e− 2 ab ∼ ments do not reflect any new dynamics beyond (4){(6). with eS(E) the density of state at energy E. Due to ho- For completeness, in supplementary material we discuss mogeneity, it does not matter where is inserted, so we Op more explicitly the story for descendant states. left the location of p implicit. In equation (4) p should be understood as aO smeared operator (f) =O f Op Sd Op with smearing function f such that the set of observables FROM LOCAL ETH TO SUBSYSTEM ETH R 2 p(f) form an algebra. In particular, the operator p shouldfO g be well-defined and has finite expectation valuesO Let us now look at the implications of (4). Using con- in physical states1. Below for notational simplicity we formal mapping (1) the matrix element E E on will continue to suppress f in (f). b p a p Sd is mapped to the Euclidean three-pointh functionjO j i We now introduce subsystemO ETH which states that for a subregion B [5] E E (8) h bjOpj ai h 1. There exists a \universal" density matrix ρB(E) L p Ψy( ) (1)Ψ (0) − b p a p hp (which depends only on B and energy E) such that = h 1 O i = CabL− ; Ψay ( )Ψ (0) Ψy( )Ψ (0) for any energy eigenstate Ea h 1 a ih b 1 b i j i q a O(S(E)) p ρ ρ (E = E ) e− (5) where C is the OPE coefficient for p appearing in jj B − B a jj ∼ ab O the operator product Ψ and Ψy, when Ψ and Ψ are a a b a b where ρB TrBc Ea Ea .
Recommended publications
  • On Thermality of CFT Eigenstates
    On thermality of CFT eigenstates Pallab Basu1 , Diptarka Das2 , Shouvik Datta3 and Sridip Pal2 1International Center for Theoretical Sciences-TIFR, Shivakote, Hesaraghatta Hobli, Bengaluru North 560089, India. 2Department of Physics, University of California San Diego, La Jolla, CA 92093, USA. 3Institut f¨urTheoretische Physik, Eidgen¨ossischeTechnische Hochschule Z¨urich, 8093 Z¨urich,Switzerland. E-mail: [email protected], [email protected], [email protected], [email protected] Abstract: The Eigenstate Thermalization Hypothesis (ETH) provides a way to under- stand how an isolated quantum mechanical system can be approximated by a thermal density matrix. We find a class of operators in (1+1)-d conformal field theories, consisting of quasi-primaries of the identity module, which satisfy the hypothesis only at the leading order in large central charge. In the context of subsystem ETH, this plays a role in the deviation of the reduced density matrices, corresponding to a finite energy density eigen- state from its hypothesized thermal approximation. The universal deviation in terms of the square of the trace-square distance goes as the 8th power of the subsystem fraction and is suppressed by powers of inverse central charge (c). Furthermore, the non-universal deviations from subsystem ETH are found to be proportional to the heavy-light-heavy p arXiv:1705.03001v2 [hep-th] 26 Aug 2017 structure constants which are typically exponentially suppressed in h=c, where h is the conformal scaling dimension of the finite energy density
    [Show full text]
  • From Quantum Chaos and Eigenstate Thermalization to Statistical
    Advances in Physics,2016 Vol. 65, No. 3, 239–362, http://dx.doi.org/10.1080/00018732.2016.1198134 REVIEW ARTICLE From quantum chaos and eigenstate thermalization to statistical mechanics and thermodynamics a,b c b a Luca D’Alessio ,YarivKafri,AnatoliPolkovnikov and Marcos Rigol ∗ aDepartment of Physics, The Pennsylvania State University, University Park, PA 16802, USA; bDepartment of Physics, Boston University, Boston, MA 02215, USA; cDepartment of Physics, Technion, Haifa 32000, Israel (Received 22 September 2015; accepted 2 June 2016) This review gives a pedagogical introduction to the eigenstate thermalization hypothesis (ETH), its basis, and its implications to statistical mechanics and thermodynamics. In the first part, ETH is introduced as a natural extension of ideas from quantum chaos and ran- dom matrix theory (RMT). To this end, we present a brief overview of classical and quantum chaos, as well as RMT and some of its most important predictions. The latter include the statistics of energy levels, eigenstate components, and matrix elements of observables. Build- ing on these, we introduce the ETH and show that it allows one to describe thermalization in isolated chaotic systems without invoking the notion of an external bath. We examine numerical evidence of eigenstate thermalization from studies of many-body lattice systems. We also introduce the concept of a quench as a means of taking isolated systems out of equi- librium, and discuss results of numerical experiments on quantum quenches. The second part of the review explores the implications of quantum chaos and ETH to thermodynamics. Basic thermodynamic relations are derived, including the second law of thermodynamics, the fun- damental thermodynamic relation, fluctuation theorems, the fluctuation–dissipation relation, and the Einstein and Onsager relations.
    [Show full text]
  • Articles and Thus Only Consider the Mo- with Solar Radiation
    Hydrol. Earth Syst. Sci., 17, 225–251, 2013 www.hydrol-earth-syst-sci.net/17/225/2013/ Hydrology and doi:10.5194/hess-17-225-2013 Earth System © Author(s) 2013. CC Attribution 3.0 License. Sciences Thermodynamics, maximum power, and the dynamics of preferential river flow structures at the continental scale A. Kleidon1, E. Zehe2, U. Ehret2, and U. Scherer2 1Max-Planck Institute for Biogeochemistry, Hans-Knoll-Str.¨ 10, 07745 Jena, Germany 2Institute of Water Resources and River Basin Management, Karlsruhe Institute of Technology – KIT, Karlsruhe, Germany Correspondence to: A. Kleidon ([email protected]) Received: 14 May 2012 – Published in Hydrol. Earth Syst. Sci. Discuss.: 11 June 2012 Revised: 14 December 2012 – Accepted: 22 December 2012 – Published: 22 January 2013 Abstract. The organization of drainage basins shows some not randomly diffuse through the soil to the ocean, but rather reproducible phenomena, as exemplified by self-similar frac- collects in channels that are organized in tree-like structures tal river network structures and typical scaling laws, and along topographic gradients. This organization of surface these have been related to energetic optimization principles, runoff into tree-like structures of river networks is not a pe- such as minimization of stream power, minimum energy ex- culiar exception, but is persistent and can generally be found penditure or maximum “access”. Here we describe the or- in many different regions of the Earth. Hence, it would seem ganization and dynamics of drainage systems using thermo- that the evolution and maintenance of these structures of river dynamics, focusing on the generation, dissipation and trans- networks is a reproducible phenomenon that would be the ex- fer of free energy associated with river flow and sediment pected outcome of how natural systems organize their flows.
    [Show full text]
  • Lecture 6: Entropy
    Matthew Schwartz Statistical Mechanics, Spring 2019 Lecture 6: Entropy 1 Introduction In this lecture, we discuss many ways to think about entropy. The most important and most famous property of entropy is that it never decreases Stot > 0 (1) Here, Stot means the change in entropy of a system plus the change in entropy of the surroundings. This is the second law of thermodynamics that we met in the previous lecture. There's a great quote from Sir Arthur Eddington from 1927 summarizing the importance of the second law: If someone points out to you that your pet theory of the universe is in disagreement with Maxwell's equationsthen so much the worse for Maxwell's equations. If it is found to be contradicted by observationwell these experimentalists do bungle things sometimes. But if your theory is found to be against the second law of ther- modynamics I can give you no hope; there is nothing for it but to collapse in deepest humiliation. Another possibly relevant quote, from the introduction to the statistical mechanics book by David Goodstein: Ludwig Boltzmann who spent much of his life studying statistical mechanics, died in 1906, by his own hand. Paul Ehrenfest, carrying on the work, died similarly in 1933. Now it is our turn to study statistical mechanics. There are many ways to dene entropy. All of them are equivalent, although it can be hard to see. In this lecture we will compare and contrast dierent denitions, building up intuition for how to think about entropy in dierent contexts. The original denition of entropy, due to Clausius, was thermodynamic.
    [Show full text]
  • Phys 344 Lecture 5 Jan. 16 2009 1 10 Wells Oscillator.Py & Helix.Py
    Phys 344 Lecture 5 Jan. 16th 2009 1 Fri. 1/16 2.4, B.2,3 More Probabilities HW5: 13, 16, 18, 21; B.8,11 Mon. 1/20 2.5 Ideal Gas HW6: 26 HW3,4,5 Wed. 1/22 (C 10.3.1) 2.6 Entropy & 2nd Law HW7: 29, 32, 38 Fri. 1/23 (C 10.3.1) 2.6 Entropy & 2nd Law (more) 10_wells_oscillator.py & helix.py (note: helix must be lowercase) BallSpring.mov Statmech.exe Didn’t get through 2.3 last time, so doing it now 2. The Second Law At the End, reassess what homework will be due Monday. Motivation / transition o Combinatorics 2.1 Two-State Systems Microstate = state of the system in terms of microscopic details. Macrostate = state of the system in terms of macroscopic variables Multiplicity = : How many Microstates are consistent with a given Macrostate. Fundamental assumption of statistical mechanics: In an isolated system in internal thermal equilibrium, all accessible microstates are equally probable. Probability: N Fair Coins N! N o N, n n! N n ! n 2.1.1 The Two-State Paramagnet N N! o N, N N N ! N N ! 2.2 The Einstein Model of a Solid o Demo. BallSpring.mov o Demo. 10_wells_oscillator.py N 1 q ! o N, q N 1 ! q ! 2.3 Thermal equilibrium of two blocks To address thermodynamic equilibrium, we need a way of describing two, interacting objects. We’ll take two Einstein Solids. We’ll begin simple, with each “solid” simply being an atom, i.e. 3 oscillators. Solid A Solid B U U A B q q A B N N A B Two single-atom blocks o We’re going to consider these two sharing a total of 4 quanta of energy, so, at any given instant, one of the atoms may have all 4, 3, 2, 1, or none of the quanta.
    [Show full text]
  • Physics Conditional Equilibrium and the Equivalence of Microcanonical
    Communications in Commun. math. Phys. 62, 279-302 (1978) Mathematical Physics © by Springer-Verlag 1978 Conditional Equilibrium and the Equivalence of Microcanonical and Grandcanonical Ensembles in the Thermodynamic Limit Michael Aizenman1*, Sheldon Goldstein2**, and Joel L. Lebowitz2*** 1 Department of Physics, Princeton University, Princeton, New Jersey 08540, USA 2 Department of Mathematics, Rutgers University, New Brunswick, New Jersey 08903, USA Abstract. Equivalence (allowing for convex combinations) of microcanonical, canonical and grandcanonical ensembles for states of classical systems is established under very mild assumptions on the limiting state. We introduce the notion of conditional equilibrium (C.E.), a property of states of infinite systems which characterizes convex combinations of limits of microcanonical ensembles. It is shown that C.E. states are, under quite general conditions, mixtures of Gibbs states. 1. Introduction Systems of infinite spatial extent [1-3] offer mathematically convenient idealiz- ations of macroscopic equilibrium systems. The statistical mechanical theory of such systems may be obtained either by considering the thermodynamic (infinite volume) limit of finite systems described by appropriate Gibbs ensembles (e.g., micro-canonical, canonical, grand-canonical, pressure) or by considering equilib- rium states of infinite systems directly. While the first route is the more physical, the latter is mathematically more direct and can often provide useful insights into the phenomena for which the large size (on a molecular scale) of macroscopic systems plays an essential role, e.g., phase-transitions. In addition the formal theory of infinite systems may offer useful mathematical tools for the study of local phenomena in macroscopic systems. Various results valid in the thermodynamic limit can be formulated as simple properties of the infinite system.
    [Show full text]
  • Does a Single Eigenstate Encode the Full Hamiltonian?
    PHYSICAL REVIEW X 8, 021026 (2018) Does a Single Eigenstate Encode the Full Hamiltonian? James R. Garrison1,2 and Tarun Grover3,4 1Department of Physics, University of California, Santa Barbara, California 93106, USA 2Joint Quantum Institute and Joint Center for Quantum Information and Computer Science, National Institute of Standards and Technology and University of Maryland, College Park, Maryland 20742, USA 3Kavli Institute for Theoretical Physics, University of California, Santa Barbara, California 93106, USA 4Department of Physics, University of California at San Diego, La Jolla, California 92093, USA (Received 31 August 2017; revised manuscript received 14 December 2017; published 30 April 2018) The eigenstate thermalization hypothesis (ETH) posits that the reduced density matrix for a subsystem corresponding to an excited eigenstate is “thermal.” Here we expound on this hypothesis by asking: For which class of operators, local or nonlocal, is ETH satisfied? We show that this question is directly related to a seemingly unrelated question: Is the Hamiltonian of a system encoded within a single eigenstate? We formulate a strong form of ETH where, in the thermodynamic limit, the reduced density matrix of a subsystem corresponding to a pure, finite energy density eigenstate asymptotically becomes equal to the thermal reduced density matrix, as long as the subsystem size is much less than the total system size, irrespective of how large the subsystem is compared to any intrinsic length scale of the system. This allows one to access the properties of the underlying Hamiltonian at arbitrary energy densities (or temperatures) using just a single eigenstate. We provide support for our conjecture by performing an exact diagonalization study of a nonintegrable 1D quantum lattice model with only energy conservation.
    [Show full text]
  • PHY294, Winter 2017, Thermal Physics Term Test
    PHY294, Winter 2017, Thermal Physics Term Test. One 8:5 × 11 inches double-sided, hand-written aid sheet allowed. Duration: 75 minutes. I. Einstein solids with small energy per oscillator Consider an Einstein solid. Consider the case when N ! 1, q ! 1, but q N; as usual, when we say N ! 1, we really mean a very large number, like 1023. In words, let both the number of oscillators and energy be large (this is the so-called thermodynamic limit), but the energy per quantum is small. Remember that the energy of the solid is E = ~!q. 1. Find an expression for the multiplicity of the Einstein solid Ω(N; q), and show that Ω(N; q) ' q eN q in this limit. 2. Find the entropy and temperature in this limit. Is the temperature small or large, compared to ~!=k? How would you then call this q N limit? 3. Find the energy as a function of the temperature and determine the heat capacity cN = 1 dE N dT N per oscillator. What is the limit of cN as T ! 0? 30 points II. Sharpness of multiplicity function Consider two Einstein solids. Let each of them consist of N oscillators, each of frequency !, so q that the quantum of energy is ~!. One of them has q1 = 2 + x quanta of energy and the other q has q2 = 2 − x quanta. In words, the total number of quanta is q, and x is the energy disbalance between the solids. Consider the thermodynamic limit of large-N and qi, i = 1; 2, but qi N, as in the previous problem.
    [Show full text]
  • Lecture 7: Ensembles
    Matthew Schwartz Statistical Mechanics, Spring 2019 Lecture 7: Ensembles 1 Introduction In statistical mechanics, we study the possible microstates of a system. We never know exactly which microstate the system is in. Nor do we care. We are interested only in the behavior of a system based on the possible microstates it could be, that share some macroscopic proporty (like volume V ; energy E, or number of particles N). The possible microstates a system could be in are known as the ensemble of states for a system. There are dierent kinds of ensembles. So far, we have been counting microstates with a xed number of particles N and a xed total energy E. We dened as the total number microstates for a system. That is (E; V ; N) = 1 (1) microstatesk withsaXmeN ;V ;E Then S = kBln is the entropy, and all other thermodynamic quantities follow from S. For an isolated system with N xed and E xed the ensemble is known as the microcanonical 1 @S ensemble. In the microcanonical ensemble, the temperature is a derived quantity, with T = @E . So far, we have only been using the microcanonical ensemble. 1 3 N For example, a gas of identical monatomic particles has (E; V ; N) V NE 2 . From this N! we computed the entropy S = kBln which at large N reduces to the Sackur-Tetrode formula. 1 @S 3 NkB 3 The temperature is T = @E = 2 E so that E = 2 NkBT . Also in the microcanonical ensemble we observed that the number of states for which the energy of one degree of freedom is xed to "i is (E "i) "i/k T (E " ).
    [Show full text]
  • Introduction
    1 Introduction Statistical mechanics is the branch of physics which aims at bridging the gap be- tween the microscopic and macroscopic descriptions of large systems of particles in interaction, by combining the information provided by the microscopic descrip- tion with a probabilistic approach. Its goal is to understand the relations existing between the salient macroscopic features observed in these systems and the prop- erties of their microscopic constituents. Equilibrium statistical mechanics is the part of this theory that deals with macroscopic systems at equilibrium and is, by far, the best understood. This book is an introduction to some classical mathematical aspects of equilib- rium statistical mechanics, based essentially on some important examples. It does not constitute an exhaustive introduction: many important aspects, discussed in a myriad of books (see those listed in Section 1.6.2 below), will not be discussed. Inputs from physics will be restricted to the terminology used (especially in this in- troduction), to the nature of the problems addressed, and to the central probabil- ity distribution used throughout, namely the Gibbs distribution. This distribution provides the probability of observing a particular microscopic state ω of the system under investigation, when the latter is at equilibrium at a fixed temperature T . It takes the form βH (ω) e− µβ(ω) , = Zβ where β 1/T , H (ω) is the energy of the microscopic state ω and Z is a normal- = β ization factor called the partition function. Saying that the Gibbs distribution is well suited to understand the phenomenol- ogy of large systems of particles is an understatement.
    [Show full text]
  • On Bose-Einstein Condensation in Any Dimension
    XA9743261 IC/96/65 INTERNATIONAL CENTRE FOR THEORETICAL PHYSICS ON BOSE-EINSTEIN CONDENSATION IN ANY DIMENSION H. Perez Rojas MIRAMARE-TRIESTE VOL 2 8 Ns 0 INTERNATIONAL ATOMIC ENERGY AGENCY UNITED NATIONS EDUCATIONAL, SCIENTIFIC AND CULTURAL ORGANIZATION IC/96/65 United Nations Educational Scientific and Cultural Organization and International Atomic Energy Agency INTERNATIONAL CENTRE FOR THEORETICAL PHYSICS ON BOSE EINSTEIN CONDENSATION IN ANY DIMENSION1 H. Perez Rojas 2 International Centre for Theoretical Physics, Trieste, Italy. ABSTRACT A general property of an ideal Bose gas as temperature tends to zero and when condi ­ tions of degeneracy are satisfied is to have an arbitrarily large population in the ground state (or in its neighborhood); thus, condensation occurs in any dimension D but for D < 2 there is no critical temperature. Some astrophysics! consequences, as well as the temperature-dependent mass case, are discussed. MIRAMARE - TRIESTE April 1996 * Submitted to Physics Letters A. ^Permanent Address: Grupo de Fisica Teorica, ICIMAF, Academia de Ciencias de Cuba, Calle E No. 309, Vedado, La Habana 4, Cuba, e-mail: [email protected]. edu.cu 1 What is Bose-Einstein condensation? At present there is a renewed interest in Bose-Einstein condensation (BEC), particularly after its experimental realization [1]. Actually, BEC is one of the most interesting prob ­ lems of quantum statistics. It occurs in a free particle Bose gas at a critical temperature Tc, and is a pure quantum phenomenon, in the sense that no interaction is assumed to exist among the particles. BEC is interesting for condensed matter (superfluidity, su­ perconductivity) but it also has increasing interest in high energy physics (electroweak phase transition, superfluidity in neutron stars).
    [Show full text]
  • Universality in Volume-Law Entanglement of Scrambled Pure Quantum States
    ARTICLE DOI: 10.1038/s41467-018-03883-9 OPEN Universality in volume-law entanglement of scrambled pure quantum states Yuya O. Nakagawa 1,2, Masataka Watanabe 2,3, Hiroyuki Fujita 1,2 & Sho Sugiura 1 A pure quantum state can fully describe thermal equilibrium as long as one focuses on local observables. The thermodynamic entropy can also be recovered as the entanglement entropy of small subsystems. When the size of the subsystem increases, however, quantum 1234567890():,; correlations break the correspondence and mandate a correction to this simple volume law. The elucidation of the size dependence of the entanglement entropy is thus essentially important in linking quantum physics with thermodynamics. Here we derive an analytic formula of the entanglement entropy for a class of pure states called cTPQ states representing equilibrium. We numerically find that our formula applies universally to any sufficiently scrambled pure state representing thermal equilibrium, i.e., energy eigenstates of non-integrable models and states after quantum quenches. Our formula is exploited as diagnostics for chaotic systems; it can distinguish integrable models from non-integrable models and many-body localization phases from chaotic phases. 1 Institute for Solid State Physics, The University of Tokyo, Kashiwa, Chiba 277-8581, Japan. 2 Department of Physics, Faculty of Science, The University of Tokyo, Bunkyo-ku, Tokyo 133-0022, Japan. 3 Kavli Institute for the Physics and Mathematics of the Universe (WPI), The University of Tokyo Institutes for Advanced Study, The University of Tokyo, Kashiwa, Chiba 277-8583, Japan. Correspondence and requests for materials should be addressed to Y.O.N. (email: [email protected]) or to S.S.
    [Show full text]