Chapter 3: Entanglement, Density Matrices, and Decoherence
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Lecture 32 Relevant Sections in Text: §3.7, 3.9 Total Angular Momentum
Physics 6210/Spring 2008/Lecture 32 Lecture 32 Relevant sections in text: x3.7, 3.9 Total Angular Momentum Eigenvectors How are the total angular momentum eigenvectors related to the original product eigenvectors (eigenvectors of Lz and Sz)? We will sketch the construction and give the results. Keep in mind that the general theory of angular momentum tells us that, for a 1 given l, there are only two values for j, namely, j = l ± 2. Begin with the eigenvectors of total angular momentum with the maximum value of angular momentum: 1 1 1 jj = l; j = ; j = l + ; m = l + i: 1 2 2 2 j 2 Given j1 and j2, there is only one linearly independent eigenvector which has the appro- priate eigenvalue for Jz, namely 1 1 jj = l; j = ; m = l; m = i; 1 2 2 1 2 2 so we have 1 1 1 1 1 jj = l; j = ; j = l + ; m = l + i = jj = l; j = ; m = l; m = i: 1 2 2 2 2 1 2 2 1 2 2 To get the eigenvectors with lower eigenvalues of Jz we can apply the ladder operator J− = L− + S− to this ket and normalize it. In this way we get expressions for all the kets 1 1 1 1 1 jj = l; j = 1=2; j = l + ; m i; m = −l − ; −l + ; : : : ; l − ; l + : 1 2 2 j j 2 2 2 2 The details can be found in the text. 1 1 Next, we consider j = l − 2 for which the maximum mj value is mj = l − 2. -
Motion of the Reduced Density Operator
Motion of the Reduced Density Operator Nicholas Wheeler, Reed College Physics Department Spring 2009 Introduction. Quantum mechanical decoherence, dissipation and measurements all involve the interaction of the system of interest with an environmental system (reservoir, measurement device) that is typically assumed to possess a great many degrees of freedom (while the system of interest is typically assumed to possess relatively few degrees of freedom). The state of the composite system is described by a density operator ρ which in the absence of system-bath interaction we would denote ρs ρe, though in the cases of primary interest that notation becomes unavailable,⊗ since in those cases the states of the system and its environment are entangled. The observable properties of the system are latent then in the reduced density operator ρs = tre ρ (1) which is produced by “tracing out” the environmental component of ρ. Concerning the specific meaning of (1). Let n) be an orthonormal basis | in the state space H of the (open) system, and N) be an orthonormal basis s !| " in the state space H of the (also open) environment. Then n) N) comprise e ! " an orthonormal basis in the state space H = H H of the |(closed)⊗| composite s e ! " system. We are in position now to write ⊗ tr ρ I (N ρ I N) e ≡ s ⊗ | s ⊗ | # ! " ! " ↓ = ρ tr ρ in separable cases s · e The dynamics of the composite system is generated by Hamiltonian of the form H = H s + H e + H i 2 Motion of the reduced density operator where H = h I s s ⊗ e = m h n m N n N $ | s| % | % ⊗ | % · $ | ⊗ $ | m,n N # # $% & % &' H = I h e s ⊗ e = n M n N M h N | % ⊗ | % · $ | ⊗ $ | $ | e| % n M,N # # $% & % &' H = m M m M H n N n N i | % ⊗ | % $ | ⊗ $ | i | % ⊗ | % $ | ⊗ $ | m,n M,N # # % &$% & % &'% & —all components of which we will assume to be time-independent. -
Singlet NMR Methodology in Two-Spin-1/2 Systems
Singlet NMR Methodology in Two-Spin-1/2 Systems Giuseppe Pileio School of Chemistry, University of Southampton, SO17 1BJ, UK The author dedicates this work to Prof. Malcolm H. Levitt on the occasion of his 60th birthaday Abstract This paper discusses methodology developed over the past 12 years in order to access and manipulate singlet order in systems comprising two coupled spin- 1/2 nuclei in liquid-state nuclear magnetic resonance. Pulse sequences that are valid for different regimes are discussed, and fully analytical proofs are given using different spin dynamics techniques that include product operator methods, the single transition operator formalism, and average Hamiltonian theory. Methods used to filter singlet order from byproducts of pulse sequences are also listed and discussed analytically. The theoretical maximum amplitudes of the transformations achieved by these techniques are reported, together with the results of numerical simulations performed using custom-built simulation code. Keywords: Singlet States, Singlet Order, Field-Cycling, Singlet-Locking, M2S, SLIC, Singlet Order filtration Contents 1 Introduction 2 2 Nuclear Singlet States and Singlet Order 4 2.1 The spin Hamiltonian and its eigenstates . 4 2.2 Population operators and spin order . 6 2.3 Maximum transformation amplitude . 7 2.4 Spin Hamiltonian in single transition operator formalism . 8 2.5 Relaxation properties of singlet order . 9 2.5.1 Coherent dynamics . 9 2.5.2 Incoherent dynamics . 9 2.5.3 Central relaxation property of singlet order . 10 2.6 Singlet order and magnetic equivalence . 11 3 Methods for manipulating singlet order in spin-1/2 pairs 13 3.1 Field Cycling . -
A Mini-Introduction to Information Theory
A Mini-Introduction To Information Theory Edward Witten School of Natural Sciences, Institute for Advanced Study Einstein Drive, Princeton, NJ 08540 USA Abstract This article consists of a very short introduction to classical and quantum information theory. Basic properties of the classical Shannon entropy and the quantum von Neumann entropy are described, along with related concepts such as classical and quantum relative entropy, conditional entropy, and mutual information. A few more detailed topics are considered in the quantum case. arXiv:1805.11965v5 [hep-th] 4 Oct 2019 Contents 1 Introduction 2 2 Classical Information Theory 2 2.1 ShannonEntropy ................................... .... 2 2.2 ConditionalEntropy ................................. .... 4 2.3 RelativeEntropy .................................... ... 6 2.4 Monotonicity of Relative Entropy . ...... 7 3 Quantum Information Theory: Basic Ingredients 10 3.1 DensityMatrices .................................... ... 10 3.2 QuantumEntropy................................... .... 14 3.3 Concavity ......................................... .. 16 3.4 Conditional and Relative Quantum Entropy . ....... 17 3.5 Monotonicity of Relative Entropy . ...... 20 3.6 GeneralizedMeasurements . ...... 22 3.7 QuantumChannels ................................... ... 24 3.8 Thermodynamics And Quantum Channels . ...... 26 4 More On Quantum Information Theory 27 4.1 Quantum Teleportation and Conditional Entropy . ......... 28 4.2 Quantum Relative Entropy And Hypothesis Testing . ......... 32 4.3 Encoding -
Density Matrix Description of NMR
Density Matrix Description of NMR BCMB/CHEM 8190 Operators in Matrix Notation • It will be important, and convenient, to express the commonly used operators in matrix form • Consider the operator Iz and the single spin functions α and β - recall ˆ ˆ ˆ ˆ ˆ ˆ Ix α = 1 2 β Ix β = 1 2α Iy α = 1 2 iβ Iy β = −1 2 iα Iz α = +1 2α Iz β = −1 2 β α α = β β =1 α β = β α = 0 - recall the expectation value for an observable Q = ψ Qˆ ψ = ∫ ψ∗Qˆψ dτ Qˆ - some operator ψ - some wavefunction - the matrix representation is the possible expectation values for the basis functions α β α ⎡ α Iˆ α α Iˆ β ⎤ ⎢ z z ⎥ ⎢ ˆ ˆ ⎥ β ⎣ β Iz α β Iz β ⎦ ⎡ α Iˆ α α Iˆ β ⎤ ⎡1 2 α α −1 2 α β ⎤ ⎡1 2 0 ⎤ ⎡1 0 ⎤ ˆ ⎢ z z ⎥ 1 Iz = = ⎢ ⎥ = ⎢ ⎥ = ⎢ ⎥ ⎢ ˆ ˆ ⎥ 1 2 β α −1 2 β β 0 −1 2 2 0 −1 ⎣ β Iz α β Iz β ⎦ ⎣⎢ ⎦⎥ ⎣ ⎦ ⎣ ⎦ • This is convenient, as the operator is just expressed as a matrix of numbers – no need to derive it again, just store it in computer Operators in Matrix Notation • The matrices for Ix, Iy,and Iz are called the Pauli spin matrices ˆ ⎡ 0 1 2⎤ 1 ⎡0 1 ⎤ ˆ ⎡0 −1 2 i⎤ 1 ⎡0 −i ⎤ ˆ ⎡1 2 0 ⎤ 1 ⎡1 0 ⎤ Ix = ⎢ ⎥ = ⎢ ⎥ Iy = ⎢ ⎥ = ⎢ ⎥ Iz = ⎢ ⎥ = ⎢ ⎥ ⎣1 2 0 ⎦ 2 ⎣1 0⎦ ⎣1 2 i 0 ⎦ 2 ⎣i 0 ⎦ ⎣ 0 −1 2⎦ 2 ⎣0 −1 ⎦ • Express α , β , α and β as 1×2 column and 2×1 row vectors ⎡1⎤ ⎡0⎤ α = ⎢ ⎥ β = ⎢ ⎥ α = [1 0] β = [0 1] ⎣0⎦ ⎣1⎦ • Using matrices, the operations of Ix, Iy, and Iz on α and β , and the orthonormality relationships, are shown below ˆ 1 ⎡0 1⎤⎡1⎤ 1 ⎡0⎤ 1 ˆ 1 ⎡0 1⎤⎡0⎤ 1 ⎡1⎤ 1 Ix α = ⎢ ⎥⎢ ⎥ = ⎢ ⎥ = β Ix β = ⎢ ⎥⎢ ⎥ = ⎢ ⎥ = α 2⎣1 0⎦⎣0⎦ 2⎣1⎦ 2 2⎣1 0⎦⎣1⎦ 2⎣0⎦ 2 ⎡1⎤ ⎡0⎤ α α = [1 0]⎢ ⎥ -
Quantum Information Theory
Lecture Notes Quantum Information Theory Renato Renner with contributions by Matthias Christandl February 6, 2013 Contents 1 Introduction 5 2 Probability Theory 6 2.1 What is probability? . .6 2.2 Definition of probability spaces and random variables . .7 2.2.1 Probability space . .7 2.2.2 Random variables . .7 2.2.3 Notation for events . .8 2.2.4 Conditioning on events . .8 2.3 Probability theory with discrete random variables . .9 2.3.1 Discrete random variables . .9 2.3.2 Marginals and conditional distributions . .9 2.3.3 Special distributions . 10 2.3.4 Independence and Markov chains . 10 2.3.5 Functions of random variables, expectation values, and Jensen's in- equality . 10 2.3.6 Trace distance . 11 2.3.7 I.i.d. distributions and the law of large numbers . 12 2.3.8 Channels . 13 3 Information Theory 15 3.1 Quantifying information . 15 3.1.1 Approaches to define information and entropy . 15 3.1.2 Entropy of events . 16 3.1.3 Entropy of random variables . 17 3.1.4 Conditional entropy . 18 3.1.5 Mutual information . 19 3.1.6 Smooth min- and max- entropies . 20 3.1.7 Shannon entropy as a special case of min- and max-entropy . 20 3.2 An example application: channel coding . 21 3.2.1 Definition of the problem . 21 3.2.2 The general channel coding theorem . 21 3.2.3 Channel coding for i.i.d. channels . 24 3.2.4 The converse . 24 2 4 Quantum States and Operations 26 4.1 Preliminaries . -
The Statistical Interpretation of Entangled States B
The Statistical Interpretation of Entangled States B. C. Sanctuary Department of Chemistry, McGill University 801 Sherbrooke Street W Montreal, PQ, H3A 2K6, Canada Abstract Entangled EPR spin pairs can be treated using the statistical ensemble interpretation of quantum mechanics. As such the singlet state results from an ensemble of spin pairs each with an arbitrary axis of quantization. This axis acts as a quantum mechanical hidden variable. If the spins lose coherence they disentangle into a mixed state. Whether or not the EPR spin pairs retain entanglement or disentangle, however, the statistical ensemble interpretation resolves the EPR paradox and gives a mechanism for quantum “teleportation” without the need for instantaneous action-at-a-distance. Keywords: Statistical ensemble, entanglement, disentanglement, quantum correlations, EPR paradox, Bell’s inequalities, quantum non-locality and locality, coincidence detection 1. Introduction The fundamental questions of quantum mechanics (QM) are rooted in the philosophical interpretation of the wave function1. At the time these were first debated, covering the fifty or so years following the formulation of QM, the arguments were based primarily on gedanken experiments2. Today the situation has changed with numerous experiments now possible that can guide us in our search for the true nature of the microscopic world, and how The Infamous Boundary3 to the macroscopic world is breached. The current view is based upon pivotal experiments, performed by Aspect4 showing that quantum mechanics is correct and Bell’s inequalities5 are violated. From this the non-local nature of QM became firmly entrenched in physics leading to other experiments, notably those demonstrating that non-locally is fundamental to quantum “teleportation”. -
Two-State Systems
1 TWO-STATE SYSTEMS Introduction. Relative to some/any discretely indexed orthonormal basis |n) | ∂ | the abstract Schr¨odinger equation H ψ)=i ∂t ψ) can be represented | | | ∂ | (m H n)(n ψ)=i ∂t(m ψ) n ∂ which can be notated Hmnψn = i ∂tψm n H | ∂ | or again ψ = i ∂t ψ We found it to be the fundamental commutation relation [x, p]=i I which forced the matrices/vectors thus encountered to be ∞-dimensional. If we are willing • to live without continuous spectra (therefore without x) • to live without analogs/implications of the fundamental commutator then it becomes possible to contemplate “toy quantum theories” in which all matrices/vectors are finite-dimensional. One loses some physics, it need hardly be said, but surprisingly much of genuine physical interest does survive. And one gains the advantage of sharpened analytical power: “finite-dimensional quantum mechanics” provides a methodological laboratory in which, not infrequently, the essentials of complicated computational procedures can be exposed with closed-form transparency. Finally, the toy theory serves to identify some unanticipated formal links—permitting ideas to flow back and forth— between quantum mechanics and other branches of physics. Here we will carry the technique to the limit: we will look to “2-dimensional quantum mechanics.” The theory preserves the linearity that dominates the full-blown theory, and is of the least-possible size in which it is possible for the effects of non-commutivity to become manifest. 2 Quantum theory of 2-state systems We have seen that quantum mechanics can be portrayed as a theory in which • states are represented by self-adjoint linear operators ρ ; • motion is generated by self-adjoint linear operators H; • measurement devices are represented by self-adjoint linear operators A. -
(Ab Initio) Pathintegral Molecular Dynamics
(Ab initio) path-integral Molecular Dynamics The double slit experiment Sum over paths: Suppose only two paths: interference The double slit experiment ● Introduce of a large number of intermediate gratings, each containing many slits. ● Electrons may pass through any sequence of slits before reaching the detector ● Take the limit in which infinitely many gratings → empty space Do nuclei really behave classically ? Do nuclei really behave classically ? Do nuclei really behave classically ? Do nuclei really behave classically ? Example: proton transfer in malonaldehyde only one quantum proton Tuckerman and Marx, Phys. Rev. Lett. (2001) Example: proton transfer in water + + Classical H5O2 Quantum H5O2 Marx et al. Nature (1997) Proton inWater-Hydroxyl (Ice) Overlayers on Metal Surfaces T = 160 K Li et al., Phys. Rev. Lett. (2010) Proton inWater-Hydroxyl (Ice) Overlayers on Metal Surfaces Li et al., Phys. Rev. Lett. (2010) The density matrix: definition Ensemble of states: Ensemble average: Let©s define: ρ is hermitian: real eigenvalues The density matrix: time evolution and equilibrium At equilibrium: ρ can be expressed as pure function of H and diagonalized simultaneously with H The density matrix: canonical ensemble Canonical ensemble: Canonical density matrix: Path integral formulation One particle one dimension: K and Φ do not commute, thus, Trotter decomposition: Canonical density matrix: Path integral formulation Evaluation of: Canonical density matrix: Path integral formulation Matrix elements of in space coordinates: acts on the eigenstates from the left: Canonical density matrix: Path integral formulation Where it was used: It can be Monte Carlo sampled, but for MD we need momenta! Path integral isomorphism Introducing a chain frequency and an effective potential: Path integral molecular dynamics Fictitious momenta: introducing a set of P Gaussian integrals : convenient parameter Gaussian integrals known: (adjust prefactor ) Does it work? i. -
Structure of a Spin ½ B
Structure of a spin ½ B. C. Sanctuary Department of Chemistry, McGill University Montreal Quebec H3H 1N3 Canada Abstract. The non-hermitian states that lead to separation of the four Bell states are examined. In the absence of interactions, a new quantum state of spin magnitude 1/√2 is predicted. Properties of these states show that an isolated spin is a resonance state with zero net angular momentum, consistent with a point particle, and each resonance corresponds to a degenerate but well defined structure. By averaging and de-coherence these structures are shown to form ensembles which are consistent with the usual quantum description of a spin. Keywords: Bell states, Bell’s Inequalities, spin theory, quantum theory, statistical interpretation, entanglement, non-hermitian states. PACS: Quantum statistical mechanics, 05.30. Quantum Mechanics, 03.65. Entanglement and quantum non-locality, 03.65.Ud 1. INTRODUCTION In spite of its tremendous success in describing the properties of microscopic systems, the debate over whether quantum mechanics is the most fundamental theory has been going on since its inception1. The basic property of quantum mechanics that belies it as the most fundamental theory is its statistical nature2. The history is well known: EPR3 showed that two non-commuting operators are simultaneously elements of physical reality, thereby concluding that quantum mechanics is incomplete, albeit they assumed locality. Bohr4 replied with complementarity, arguing for completeness; thirty years later Bell5, questioned the locality assumption6, and the conclusion drawn that any deeper theory than quantum mechanics must be non-local. In subsequent years the idea that entangled states can persist to space-like separations became well accepted7. -
Quantum Mechanics
Quantum Mechanics Richard Fitzpatrick Professor of Physics The University of Texas at Austin Contents 1 Introduction 5 1.1 Intendedaudience................................ 5 1.2 MajorSources .................................. 5 1.3 AimofCourse .................................. 6 1.4 OutlineofCourse ................................ 6 2 Probability Theory 7 2.1 Introduction ................................... 7 2.2 WhatisProbability?.............................. 7 2.3 CombiningProbabilities. ... 7 2.4 Mean,Variance,andStandardDeviation . ..... 9 2.5 ContinuousProbabilityDistributions. ........ 11 3 Wave-Particle Duality 13 3.1 Introduction ................................... 13 3.2 Wavefunctions.................................. 13 3.3 PlaneWaves ................................... 14 3.4 RepresentationofWavesviaComplexFunctions . ....... 15 3.5 ClassicalLightWaves ............................. 18 3.6 PhotoelectricEffect ............................. 19 3.7 QuantumTheoryofLight. .. .. .. .. .. .. .. .. .. .. .. .. .. 21 3.8 ClassicalInterferenceofLightWaves . ...... 21 3.9 QuantumInterferenceofLight . 22 3.10 ClassicalParticles . .. .. .. .. .. .. .. .. .. .. .. .. .. .. 25 3.11 QuantumParticles............................... 25 3.12 WavePackets .................................. 26 2 QUANTUM MECHANICS 3.13 EvolutionofWavePackets . 29 3.14 Heisenberg’sUncertaintyPrinciple . ........ 32 3.15 Schr¨odinger’sEquation . 35 3.16 CollapseoftheWaveFunction . 36 4 Fundamentals of Quantum Mechanics 39 4.1 Introduction .................................. -
Chapter 2 Outline of Density Matrix Theory
Chapter 2 Outline of density matrix theory 2.1 The concept of a density matrix Aphysical exp eriment on a molecule usually consists in observing in a macroscopic 1 ensemble a quantity that dep ends on the particle's degrees of freedom (like the measure of a sp ectrum, that derives for example from the absorption of photons due to vibrational transitions). When the interactions of each molecule with any 2 other physical system are comparatively small , it can b e describ ed by a state vector j (t)i whose time evolution follows the time{dep endent Schrodinger equation i _ ^ j (t)i = iH j (t)i; (2.1) i i ^ where H is the system Hamiltonian, dep ending only on the degrees of freedom of the molecule itself. Even if negligible in rst approximation, the interactions with the environment usually bring the particles to a distribution of states where many of them b ehave in a similar way b ecause of the p erio dic or uniform prop erties of the reservoir (that can just consist of the other molecules of the gas). For numerical purp oses, this can 1 There are interesting exceptions to this, the \single molecule sp ectroscopies" [44,45]. 2 Of course with the exception of the electromagnetic or any other eld probing the system! 10 Outline of density matrix theory b e describ ed as a discrete distribution. The interaction b eing small compared to the internal dynamics of the system, the macroscopic e ect will just be the incoherent sum of the observables computed for every single group of similar particles times its 3 weight : 1 X ^ ^ < A>(t)= h (t)jAj (t)i (2.2) i i i i=0 If we skip the time dep endence, we can think of (2.2) as a thermal distribution, in this case the would b e the Boltzmann factors: i E i k T b e := (2.3) i Q where E is the energy of state i, and k and T are the Boltzmann constant and the i b temp erature of the reservoir, resp ectively .