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The transfer of information between different physical forms is a central theme in communication and computation, for example between processing entities and memory. Nowhere is this more crucial than in quantum computation [1], where great effort must be taken to protect the integrity of a fragile quantum bit (qubit) [2]. However, transfer of quantum information is particularly challenging, as the process must remain coherent at all times to preserve the quantum nature of the information [3]. Here we demonstrate the coherent transfer of a superposition state in an electron spin 'processing' qubit to a nuclear spin 'memory' qubit, using a combination of microwave and radiofrequency pulses applied to 31 P donors in an isotopically pure 28 Si crystal [4,5]. The state is left in the nuclear spin on a timescale that is long compared with the electron decoherence time and then coherently transferred back to the electron spin, thus demonstrating the 31 P nuclear spin as a solid-state quantum memory. The overall store/readout fidelity is about 90%, attributed to imperfect rotations which can be improved through the use of composite pulses [6]. The coherence lifetime of the quantum memory element at 5.5 K exceeds one second.Classically, transfer of information can include a copying step, facilitating the identification and correction of errors. However, the no-cloning theorem limits the ability to faithfully copy quantum states across different degrees of freedom [7]; thus error correction becomes more challenging than for classical information and the transfer of information must take place directly. Experimental demonstrations of such transfer include moving a trapped ion qubit in and out of a decoherence-free subspace for storage purposes [8] and optical measurements of NV centres in diamond [9].Nuclear spins are known to benefit from long coherence times compared to electron spins, but are slow to manipulate and suffer from weak thermal polarisation. A powerful model for quantum computation is thus one in which electron spins are used for processing and readout while nuclear spins are used for storage. The storage element can be a single, well-defined nuclear spin, or perhaps a bath of nearby nuclear spins [10]. 31 P donors in silicon provide an ideal combination of long-lived spin-1/2 electron [11] and nuclear spins [12], with the additional advantage of integration with existing technologies [4] and the possibility of single spin detection by electrical measurement [13,14,15]. Direct measurement of the 31 P nuclear spin by NMR has only been possible at very high doping levels (e.g. near the metal insulator transition [16]). Instead, electron-nuclear double resonance (ENDOR) can be used to excite both the electron and nuclear spin associated with the donor site, and measure the nuclear spin via the electron [17]. This was recently used to measure the nuclear spin-lattice relaxation time T 1n , which was found to follow the electron relaxation time T 1e over the range 6 to 12 K with the relationship T 1n ≈ 250T 1e [5,...

We study optically driven Rabi rotations of a quantum dot exciton transition between 5 and 50 K, and for pulse areas of up to 14π. In a high driving field regime, the decay of the Rabi rotations is nonmonotonic, and the period decreases with pulse area and increases with temperature. By comparing the experiments to a weak-coupling model of the exciton-phonon interaction, we demonstrate that the observed renormalization of the Rabi frequency is induced by fluctuations in the bath of longitudinal acoustic phonons, an effect that is a phonon analogy of the Lamb shift.

In order to model realistic quantum devices it is necessary to simulate quantum systems strongly coupled to their environment. To date, most understanding of open quantum systems is restricted either to weak system–bath couplings or to special cases where specific numerical techniques become effective. Here we present a general and yet exact numerical approach that efficiently describes the time evolution of a quantum system coupled to a non-Markovian harmonic environment. Our method relies on expressing the system state and its propagator as a matrix product state and operator, respectively, and using a singular value decomposition to compress the description of the state as time evolves. We demonstrate the power and flexibility of our approach by numerically identifying the localisation transition of the Ohmic spin-boson model, and considering a model with widely separated environmental timescales arising for a pair of spins embedded in a common environment.

Quantum information processing offers fundamental improvements over classical information processing, such as computing power, secure communication, and high-precision measurements. However, the best way to create practical devices is not yet known. This textbook describes the techniques that are likely to be used in implementing optical quantum information processors.After developing the fundamental concepts in quantum optics and quantum information theory, this book shows how optical systems can be used to build quantum computers according to the most recent ideas. It discusses implementations based on single photons and linear optics, optically controlled atoms and solid-state systems, atomic ensembles, and optical continuous variables.This book is ideal for graduate students beginning research in optical quantum information processing. It presents the most important techniques of the field using worked examples and over 120 exercises. Hardback Cambridge University Press has no responsibility for the persistence or accuracy of URLs for external or third-party internet websites referred to in this publication, and does not guarantee that any content on such websites is, or will remain, accurate or appropriate.

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We give three methods for entangling quantum states in quantum dots. We do this by showing how to tailor the resonant energy (Förster-Dexter) transfer mechanisms and the biexciton binding energy in a quantum dot molecule. We calculate the magnitude of these two electrostatic interactions as a function of dot size, interdot separation, material composition, confinement potential and applied electric field by using an envelope function approximation in a two-cuboid dot molecule. In the first implementation, we show that it is desirable to suppress the Förster coupling and to create entanglement by using the biexciton energy alone. We show how to perform universal quantum logic in a second implementation which uses the biexciton energy together with appropriately tuned laser pulses: by selecting appropriate materials parameters high fidelity logic can be achieved. The third implementation proposes generating quantum entanglement by switching the Förster interaction itself. We show that the energy transfer can be fast enough in certain dot structures that switching can occur on a timescale which is much less than the typical decoherence times.

Abstract. Molecular structures appear to be natural candidates for a quantum technology: individual atoms can support quantum superpositions for long periods, and such atoms can in principle be embedded in a permanent molecular scaffolding to form an array. This would be true nanotechnology, with dimensions of order of a nanometre. However, the challenges of realising such a vision are immense. One must identify a suitable elementary unit and demonstrate its merits for qubit storage and manipulation, including input / output. These units must then be formed into large arrays corresponding to an functional quantum architecture, including a mechanism for gate operations. Here we report our efforts, both experimental and theoretical, to create such a technology based on endohedral fullerenes or 'buckyballs'. We describe our successes with respect to these criteria, along with the obstacles we are currently facing and the questions that remain to be addressed.