Control of single spin in Markovian environment The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. Citation Yuan, Haidong. "Control of single spin in Markovian environment ." Proceedings of the Joint 48th IEEE Conference on Decision and Control and 28th Chinese Control Conference Shanghai, P.R. China, December 16-18, 2009. As Published http://dx.doi.org/10.1109/CDC.2009.5400712 Publisher Institute of Electrical and Electronics Engineers Version Final published version Accessed Thu May 26 08:55:42 EDT 2016 Citable Link http://hdl.handle.net/1721.1/74601 Terms of Use Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. Detailed Terms Joint 48th IEEE Conference on Decision and Control and 28th Chinese Control Conference Shanghai, P.R. China, December 16-18, 2009 WeC11.5 Control of single spin in Markovian environment Haidong Yuan∗ Abstract equation, which takes the form ρ̇ = −i[H(t), ρ] + L(ρ) In this article we study the control of single spin in Markovian environment. Given an initial state, we compute all the possible states to which the spin can be driven at arbitrary time, under the assumption that fast unitary operations on the single spin are available. (1) where −i[H, ρ] is the unitary evolution of the quantum system and L(ρ) is the dissipative part of the evolution. The term L(ρ) is linear in ρ and is given by the Lindblad form [32, 34], 1 L(ρ) = ∑ aαβ (Fα ρFβ† − {Fβ† Fα , ρ}), 2 ij 1. Introduction where Fα , Fβ are the Lindblad operators. Eq. (1) has the following three well known properties: 1) Tr(ρ) remains unity for all time, 2) ρ remains a Hermitian matrix, and 3) ρ stays positive semi-positive definite, i.e. that ρ never develops non-negative eigenvalues. In the last two decades, control theory has been applied to an increasingly wide number of problems in physics and chemistry whose dynamics are governed by the time-dependent Schrödinger equation (TDSE), including control of chemical reactions [1, 2, 3, 5, 6, 7, 8, 9], state-to-state population transfer [10, 11, 12, 13], shaped wavepackets [14], NMR spin dynamics [15], Bose-Einstein condensation [16, 17, 18], quantum computing [19, 20, 21], oriented rotational wavepackets [22], etc. [23, 24]. More recently, there has been vigorous effort in studying the control of open quantum systems which are governed by Lindblad equations, where the central object is the density matrix, rather than the wavefunction [25, 26, 27, 28, 29, 30, 31]. The Lindblad equation is an extension of the TDSE that allows for the inclusion of dissipative processes. In this article, we study two level systems governed by the controlled Lindblad equation, we will compute all the possible states to which the systems can be driven at arbitrary time, under the assumption that fast unitary operations on the system are available. 2.2. Formulation of the Control Problem The problem we address in this paper is to compute all the density matrices the system can reach for the quantum dissipative system which evolves under the Lindblad equation of motion given by eq. (1). We assume that we can apply any desired sequence of unitary transformations to the system, over a time scale of its coupling to the bath. For the purpose of this paper, we will confine our attention to two level systems, such as, e.g., a two level atom where the Hamiltonian H(t) is a time varying dipole term arising from a high bandwidth applied lase field. Our results will be largely generalizable to systems with arbitrary dimension. 3. Reformulation of the Problem in Terms of the Spectrum of ρ 2. Setting up the control problem In this section we develop a general formalism that highlights the cooperative interplay between Hamiltonian and dissipative dynamics. Following [27, 4], we assume that the action of the control Hamiltonian can be produced on a time scale fast compared with dissipation. We assume that the control Hamiltonian H(t) can produce any unitary transformation U ∈ SU(2) in the 2−level system, i.e. the system of interest is unitarily controllable. Combining these two assumptions we 2.1. The system equations of motion and the Lindblad formula for dissipation Let ρ denote the density matrix of an quantum system. The density matrix evolves under the Lindblad ∗ Haidong Yuan is with the department of Mechanical Engineering, Massachusetts Institute of Technology. 978-1-4244-3872-3/09/$25.00 ©2009 IEEE 2498 WeC11.5 4. Reachable set for single spin have that any unitary transformation can be produced on the system in negligible time compared to the dissipation. The above dynamical assumptions lead to another very important simplification. Since we have assumed that all unitary transformations in SU(2) can be produced instantaneously, this includes bringing the density matrix into diagonal form. As a result, the different elements of each orbit can be considered redundant, and the orbit of ρ can be completely represented by its diagonal form, or ’spectrum’, λ (ρ). This suggests reformulating the control problem entirely in terms of the spectrum, rather than in terms of ρ itself. The key step in this reformulation is to replace the equation of motion for ρ, eq. (1), with an equation of motion for the spectrum. We do this in the next section. The controls will enter into the equation in a modified way that gives additional insight into the interplay of Hamiltonian and dissipative dynamics. Let Λ be its associated diagonal form of density matrix ρ. Substitute ρ(t) = U(t)Λ(t)U † (t) into Eq.(1), we get 4.1. Examples Let’s first work out two examples. We first study the single spin with pure decoherence in the z-basis. In this case, L(ρ) = −γ[σz , [σz , ρ]] So Λ̇(t) =diag(U † L(UΛU † )U) =diag(−U † γ[σz , [σz ,UΛU † ]]U) † =diag(−γ[U σzU, [U σzU, Λ]]) We can write 1 Λ(t) = I + λ (t)σz 2 where λ (t) ∈ [0, 21 ], and U † (t)σzU(t) = a1 (t)σx + a2 (t)σy + a3 (t)σz where ∑3i=1 a2i (t) = 1. Substitute these into above equations, we get ρ̇(t) =U̇(t)Λ(t)U † (t) +U(t)Λ̇(t)U † (t) λ̇ (t) = −4γ(a21 (t) + a22 (t))λ † +U(t)Λ(t)U̇ (t) (2) +U(t)Λ(t)U † (t)iH 0 (t) −4γ(a21 (t) + a22 (t))dt]λ (0). Note that the quantity a21 (t) + a22 (t) ∈ [0, 1], and by choosing appropriate U(t), it can be any value in this interval. So at time T , λ (T ) can be any value in [exp(−4γT )λ (0), λ (0)], i.e., the reachable set for the single spin in this case is = − i[H(t),U(t)Λ(t)U † (t)] + L[U(t)Λ(t)U † (t)] where H 0 (t) is defined by U̇(t) = −iH 0 (t)U(t). We obtain 1 ρ(T ) = {U( I + λ (T )σz )U † | 2 (7) λ (T ) ∈ [exp(−4γT )λ (0), λ (0)],U ∈ SU(2)} Λ̇(t) =U † (t){−i[H(t) − H 0 (t),U(t)Λ(t)U † (t)] (3) Let’s look at another example with both longitudinal and transverse relaxation. +U † (t)L[U(t)Λ(t)U † (t)]U(t) L(ρ) = −γ1 [σz , [σz , ρ]] − γ2 [σx , [σx , ρ]] Note that the left side of the above equation is a diagonal matrix, so for the right side we only need to keep the diagonal part. It is easy to see that the diagonal part is zero for the first term, thus we get Λ̇(t) = diag(U † (t)L[U(t)Λ(t)U†(t)]U(t)) Z T λ (T ) = exp[ 0 = − i[H 0 (t),U(t)Λ(t)U † (t)] +U(t)Λ̇(t)U † (t) = − i[U † (t)(H(t) − H 0 (t))U(t), Λ(t)] (6) so = − iH 0 (t)U(t)Λ(t)U † (t) +U(t)Λ̇(t)U † (t) + L[U(t)Λ(t)U † (t)]}U(t) (5) † In this case Λ̇(t) =diag(U † L(UΛU † )U) =diag(−U † γ1 [σz , [σz ,UΛU † ]]U (4) −U † γ2 [σx , [σx ,UΛU † ]]U) † † =diag(−γ1 [U σzU, [U σzU, Λ]] where we use diag(A) denote a diagonal matrix whose diagonal entries are the same as matrix A. − γ2 [U † σxU, [U † σxU, Λ]]) 2499 (8) WeC11.5 known as the GKS(Gorini, Kossakowski and Sudarshan) matrix [33], is semi-positive definite. For the moment assume that the Markovian quantum dynamics is unital, which just means L(I) = 0. In the single spin case, this is equivalent to the condition that all the entries of the GKS matrix are real numbers[40]. Again we write 1 Λ(t) = I + λ (t)σz 2 where λ (t) ∈ [0, 12 ], and U † (t)σzU(t) = a1 (t)σx + a2 (t)σy + a3 (t)σz U † (t)σxU(t) = b1 (t)σx + b2 (t)σy + b3 (t)σz Λ̇(t) = diag(U † L(UΛU † )U) where ∑3i=1 a2i (t) = 1, ∑3i=1 b2i (t) = 1 and ∑3i=1 ai bi = 0. Substitute these into the equation, we get = diag(∑aαβ (U † Fα UΛU † Fβ†U λ̇ (t) = [−4γ1 (a21 (t) + a22 (t)) − 4γ2 (b21 (t) + b22 (t))]λ (9) 1 − {U † Fβ†UU † Fα U, Λ})) 2 = diag(∑aαβ (U † Fα UΛU † Fβ U αβ As a3 b3 = −a1 b1 − a2 b2 , αβ (a3 b3 )2 = (a1 b1 + a2 b2 )2 ≤ (a21 + a22 )(b21 + b22 ) = (1 − a23 )(1 − b23 ) (11) 1 − {U † Fβ UU † Fα U, Λ})) 2 (10) = 1 − a23 − b23 + a23 b23 For the last step we just used the fact that Fβ is a Pauli matrix which is Hermitian. Now We get a23 + b23 ≤ 1, so U † Fα U = cαγ Fγ 1 ≤ a21 + a22 + b21 + b22 ≤ 2 cxx cxy cxz where C = cyx cyy cyz ∈ SO(3) is the adjoint czx czy czz representation of U. Substituting these expressions into equation(11), we obtain Assume γ1 ≥ γ2 , then 4γ1 (a21 (t)+a22 (t))+4γ2 (b21 (t)+b22 (t)) ∈ [4γ2 , 4(γ1 +γ2 )] From this, it is easy to see that at time T , λ (T ) ∈ [exp(−4(γ1 + γ2 )T )λ (0), exp(−4γ2 T )λ (0)], so the reachable set for the single spin in this case is 1 Λ̇(t) = diag(∑ a0αβ (Fα ΛFβ − {Fβ Fα , Λ})), 2 αβ 1 ρ(T ) = {U( I + λ (T )σz )U † |λ (T ) ∈ 2 [exp(−4(γ1 + γ2 )T )λ (0), exp(−4γ2 T )λ (0)],U ∈ SU(2)} where 4.2. General case is the transformed GKS matrix, i.e., (12) a0αβ = cγα aγ µ cµβ A0 = CT AC The examples above are just two special cases of the following general result. Take the general expression of the master equation Substituting Λ(t) = 12 I + λ (t)σz into equation (12), we obtain the dynamics for λ (t), ρ̇ = −i[H, ρ] + L(ρ) λ̇ (t) = −(a0xx + a0yy )λ (t) where Using Schur and Horn’s theorem on majorization (see appendix), we obtain 1 L(ρ) = ∑ aαβ (Fα ρFβ† − {Fβ† Fα , ρ}) 2 αβ µ3 + µ2 ≤ a0xx + a0yy ≤ µ2 + µ1 For the single spin, we can take the basis {Fα } as normalized Pauli spin operators √12 {σx , σy , σz }. The coefficient matrix axx axy axz A = ayx ayy ayz azx azy azz where µ1 ≥ µ2 ≥ µ3 are eigenvalues of the GKS matrix. From this it is easy to see that at time T , all the values λ (T ) can be are [e−(µ1 +µ2 )T λ (0), e−(µ2 +µ3 )T λ (0)] 2500 WeC11.5 Let’s look at the right side of the above equation to see what value it can take. As we have shown before, So the reachable set for the single spin under unital master quantum dynamics is 1 0 2 + λ (T ) ρ(T ) = {U U † |λ (T ) ∈ 1 0 − λ (T ) 2 1 ≤ a21 (t) + a22 (t) + b21 (t) + b22 (t) ≤ 2 So [e−(µ1 +µ2 )T λ (0), e−(µ2 +µ3 )T λ (0)],U ∈ SU(2)} 1 −8[ + λ (t)] ≤ − 4(a21 (t) + a22 (t) + b21 (t) + b22 (t))× 2 1 (17) ( + λ (t)) 2 1 ≤ − 4[ + λ (t)] 2 Important examples of unital master equation includes phase damping and depolarizing, whose GKS matrix is just γI(I is the identity matrix). But there is another important decoherence mechanism which is not unital—amplitude damping, which models the spontaneous emission from |1i to |0i, we will study it in the next section. And 2[a2 (t) + b1 (t)]2 + 2[a1 (t) − b2 (t)]2 ≥ 0, so 5. Two level dissipative system 1 γ[−4(a21 (t) + a22 (t) + b21 (t) + b22 (t))( + λ (t)) 2 1 + 2[a2 (t) + b1 (t)]2 + 2[a1 (t) − b2 (t)]2 ] ≥ −8γ[ + λ (t)] 2 The Lindblad form for two level system with spontaneous emission from |1i to |0i is given by L(ρ) = 2γσ− ρσ+ − γ{σ+ σ− , ρ} = γ([σ− ρ, σ+ ] + [σ− , ρσ+ ]) and the equality is achievable at a1 = b2 = 1, a2 = b1 = 0, which gives the lower bound of dtd ( 12 + λ (t)). Now let’s find the upper-bound. Suppose (13) a21 (t) + a22 (t) + b21 (t) + b22 (t) = c where where c ∈ [1, 2], as σ+ = σx + iσy = σ− = σx − iσy = 1 2, 0 0 2 0 0 2 0 0 (a2 + b1 )2 + (a1 − b2 )2 ≤2(a21 (t) + a22 (t) + b21 (t) + b22 (t)) (14) =2c (15) We get Similarly we write Λ(t) = 21 I + λ (t)σz , 0 ≤ λ (t) ≤ and γ{−4(a21 (t) + a22 (t) + b21 (t) + b22 (t))× 1 [ + λ (t)] + 2(a2 + b1 )2 + 2(a1 − b2 )2 } 2 1 ≤ γ{−4c[ + λ (t)] + 4c} 2 1 = 4γc[ − λ (t)] 2 1 ≤ 8γ[ − λ (t)] 2 U † (t)σxU(t) = a1 (t)σx + a2 (t)σy + a3 (t)σz U † (t)σyU(t) = b1 (t)σx + b2 (t)σy + b3 (t)σz where ∑3i=1 a2i (t) = 1, ∑3i=1 b2i (t) = 1 and ∑3i=1 ai bi = 0. Substituting these into the equation Λ̇(t) = diag(U † L(UΛU † )U), The equality is achievable at a2 = b1 = 1, a1 = b2 = 0, which gives the upper bound. By connecting property, we know that dtd ( 12 + λ (t)) can take any value in we obtain λ̇ (t) =γ[−4(a21 (t) + a22 (t) + b21 (t) + b22 (t))λ + 4(a2 (t)b1 (t) − a1 (t)b2 (t))] (18) (16) 1 1 [−8γ( + λ (t)), 8γ( − λ (t))] 2 2 It is convenient to study the dynamics of 12 + λ (t): d 1 ( + λ (t)) = γ{−4[a21 (t) + a22 (t) + b21 (t) + b22 (t)]× dt 2 1 ( + λ (t)) + 2[a2 (t) + b1 (t)]2 + 2[a1 (t) − b2 (t)]2 } 2 2501 With this, we can find the reachable set for λ (T ). First for the lower bound, we always take the right side of eq.( 17) to be the smallest: d 1 1 [ + λ (t)] = −8γ[ + λ (t)] dt 2 2 WeC11.5 So the presence of pure decoherence, and of decoherence and relaxation. In the presence of pure decoherence, the time evolution is unital, and tends inevitably towards the fully mixed state. Coherent control can only delay this process and achieve a variety of less than fully mixed states at various times along the way. The presence of relaxation in addition to decoherence allows a richer set of states to attained by playing decoherence (which drives the system to a fully mixed state ) and relaxation (which drives the system to a pure state) off against each other. 1 1 + λ (T ) = exp(−8γT )[ + λ (0)] 2 2 1 1 λ (T ) = exp(−8γT )[ + λ (0)] − 2 2 Similarly for the upper bound: d 1 1 [ + λ (t)] = 8γ[ − λ (t)] dt 2 2 1 = −8γ[ + λ (t)] + 8γ 2 (19) The solution in this case is A. Majorization 1 1 + λ (T ) = exp(−8γT )( + λ (0)) 2 2 Z T + exp(−8γT ) 8γ exp(8γt)dt (20) 0 1 = exp(−8γT )( + λ (0)) + 1 − exp(−8γT ) 2 For an element x = (x1 , ..., xk )T of Rk we denote by = (x1↓ , ..., xk↓ )T a permutation of x so that xi↓ ≥ x↓j if i < j, where 1 ≤ i, j ≤ k. x↓ Definition 1 (majorization) A vector x ∈ Rk is majorized by a vector y ∈ Rk (denoted x ≺ y), if So 1 1 λ (T ) = exp(−8γT )(− + λ (0)) + 2 2 Thus the reachable set for this system is d ∑ x↓j ≤ j=1 1 ρ(T ) = {U[ I + λ (T )σz ]U † |U ∈ SU(2), 2 1 1 λ (T ) ∈ [max{0, exp(−8γT )[ + λ (0)] − }, (21) 2 2 1 1 exp(−8γT )(− + λ (0)) + ]} 2 2 The intuitive interpretation of this is as follows. For times short compared with 1γ , the reachable spectra are close to the original spectrum. 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