Polarization transfers from an electron spin to a nuclear spin are essential for various physical tasks, such as dynamic nuclear polarization in nuclear magnetic resonance and quantum information processing on hybrid electron-nuclear spin systems. We present time-optimal schemes for electron-nuclear polarization transfers which improve on conventional approaches, and we thereby establish an important class of faster controls. We highlight how time-optimal polarization transfers and their optimality are related to the time optimality of unitary transformations. Moreover, our work develops generally applicable analytic methods for analyzing the limits in controlling quantum systems.
Polarization transfers from an electron spin to a nuclear spin are essential for various physical tasks, such as dynamic nuclear polarization in nuclear magnetic resonance and quantum information processing on hybrid electron-nuclear spin systems. We present time-optimal schemes for electron-nuclear polarization transfers which improve on conventional approaches, and we thereby establish an important class of faster controls. We highlight how time-optimal polarization transfers and their optimality are related to the time optimality of unitary transformations. Moreover, our work develops generally applicable analytic methods for analyzing the limits in controlling quantum systems.
We study control of electron-nuclear spin dynamics at magnetic field strengths where the Larmor frequency of the nucleus is comparable to the hyperfine coupling strength. The quantization axis for the nuclear spin differs from the static B0 field direction and depends on the state of the electron spin. The quantization axis can be switched by flipping the state of electron spin, allowing for universal control of nuclear spin states. We show that by performing a sequence of flips (each followed by a suitable delay), we can perform any desired rotation of the nuclear spin, which can also be conditioned on the state of the electron spin. These operations, combined with electron spin rotations, can be used to synthesize any unitary transformation of the coupled electron-nuclear spin system. We discuss how these methods can be used for design of experiments for transfer of polarization from the electron to the nuclear spins.
With the development of quantum information science, the active manipulation of quantum systems is becoming an important research frontier. To build realistic quantum information processors, one of the challenges is to implement arbitrary desired operations with high precision on quantum systems. A large number of quantum control methods and relevant numerical techniques have been put forward in recent years, such as quantum optimal control and quantum feedback control. Nuclear magnetic resonance (NMR) spin systems offer an excellent testbed to develop benchmark tools and techniques for controlling quantum systems. In this review paper, we briefly introduce some of the basic control ideas developed for NMR systems in recent years. We first explain, for the liquid spin systems, the physics of various couplings and the causes of relaxation effects. These mechanisms govern the system dynamics, and thus are crucial for constructing rigorous and efficient control models. We also identify three types of available control means: 1) raido-frequency fields as coherent controls; 2) phase cycling, gradient fields and relaxation effects as non-unitary controls; 3) radiation damping effect as feedback control mechanism. Then, we elucidate some important control tasks, which may arise from the conventional NMR spectroscopy (e.g., pulse design and polarization transfer) or from quantum information science (e.g., algorithmic cooling and pseudo-pure state preparation). In the last part, we review some of the most important control methods that are applicable to NMR control tasks. For systems with a relatively small number of spins, it is possible to use analytic optimal control theory to realize the target unitary operations. However, for larger systems, numerical methods are necessary. The gradient ascent pulse engineering algorithm and pulse compiler techniques are the most successful techniques for implementing complicated quantum networks currently. There are some interesting topics of utilizing radiation damping and relaxation effects to achieve more powerful controls. Finally, we give an outline of the possible future work.
In this paper, we study the design of pulse sequences for nuclear magnetic resonance spectroscopy as a problem of time optimal control of the unitary propagator. Radio-frequency pulses are used in coherent spectroscopy to implement a unitary transfer between states. Pulse sequences that accomplish a desired transfer should be as short as possible in order to minimize the effects of relaxation and to optimize the sensitivity of the experiments. Here, we give an analytical characterization of such time optimal pulse sequences applicable to coherence transfer experiments in multiple-spin systems. We have adopted a general mathematical formulation, and present many of our results in this setting, mindful of the fact that new structures in optimal pulse design are constantly arising. From a general control theory perspective, the problems we want to study have the following character. Suppose we are given a controllable right invariant system on a compact Lie group. What is the minimum time required to steer the system from some initial point to a specified final point? In nuclear magnetic resonance (NMR) spectroscopy and quantum computing, this translates to, what is the minimum time required to produce a unitary propagator? We also give an analytical characterization of maximum achievable transfer in a given time for the two-spin system.
In this thesis, we study methods for optimal manipulation of coupled spin dynamics in the presence of relaxation. We use these methods to compute analytical upper bounds for the efficiency of coherence and polarization transfer between coupled nuclear spins in multidimensional nuclear magnetic resonance (NMR) experiments, under the presence of relaxation. We derive relaxation optimized pulse sequences which achieve or approach these bounds and maximize the sensitivity of the experiments. The two systems examined in detail in this thesis, arising in the context of protein NMR spectroscopy, are a coupled heteronuclear spin pair and an Ising spin chain. New schemes for coherence and polarization transfer are found, which yield substantial gains in transfer efficiency, compared to the traditionally used pulse sequences. From the standpoint of mathematical control theory, the problems arising in connection with optimal manipulation of dissipative quantum dynamics, motivate the study of a class of dissipative bilinear control systems and the computation of their reachable sets. For these systems we show that the optimal solution, corresponding to the maximization of transfer efficiency, and the reachable set can be found by solving a semidefinite program.
The goal of this project was to improve our control over nuclear spins in the solid state, and to extend this control to coupled electron-nuclear spins. Our key results are summarized below. 1. We extended the control techniques developed in liquid state NMR quantum information processing to the control of a three-qubit solid state NMR quantum information processor. 2. To explore multi-body spin dynamics and their sensitivity to decoherence, we have measured the decay of NMR multiple quantum coherence intensities in the presence and absence of the dipolar Hamiltonian, in a cubic and a one-dimensional spin system. 3. We also studied the transport of polarization in the one-dimensional fluoroapatite system, both experimentally and theoretically, and created special states in which the polarization is localized to the ends of the chain. This enables both universal Quantum Computing and Quantum Simulation in 1-D systems. 4. We devised a novel scheme for electron-nuclear quantum information processing that exploits the anisotropic hyperfine coupling. This scheme enables universal control over a 1-electron, N-nuclear spin system, addressing only a single electron spin transition. Not having to address the nuclear spins directly significantly speeds up the control. We designed and fabricated a pulsed electron spin resonance spectrometer, along with a cryogenic probe which we used to experimentally implement this scheme on a single crystal sample of irradiated malonic acid. 5. We demonstrated the role of nuclear spin dipolar diffusion in dynamic nuclear polarization (DNP) experiments, in dielectric samples with abundant nuclear spins. We achieved a 29Si polarization of 8.3% at 66 GHz and 1.1 K in single crystal P-doped, the highest ever reported, using DNP.
Experiments in coherent spectroscopy correspond to control of quantum-mechanical ensembles guiding them from initial to final target states. The control inputs (pulse sequences) that accomplish these transfers should be designed to minimize the effects of relaxation and to optimize the sensitivity of the experiments. For example in Nuclear Magnetic Resonance (NMR) spectroscopy, a question of fundamental importance is what is the maximum efficiency of polarization or coherence transfer between coupled spins in the presence of relaxation. Furthermore, what is the optimal pulse sequence which achieves this efficiency? This letter is a continuation of our previous work on the above problems. Here, we attempt to answer these questions for an Ising spin chain, under the presence of transverse relaxation. The methods presented in this paper are expected to find applications not only in coherent spectroscopy but also in quantum information processing.