Abstract. We analyse the off-resonant Raman interaction of a single broadband photon, copropagating with a classical 'control' pulse, with an atomic ensemble. It is shown that the classical electrodynamical structure of the interaction guarantees canonical evolution of the quantum mechanical field operators. This allows the interaction to be decomposed as a beamsplitter transformation between optical and material excitations on a mode-by-mode basis. A single, dominant modefunction describes the dynamics for arbitrary control pulse shapes. Complete transfer of the quantum state of the incident photon to a collective dark state within the ensemble can be achieved by shaping the control pulse so as to match the dominant mode to the temporal mode of the photon. Readout of the material excitation, back to the optical field, is considered in the context of the symmetry connecting the input and output modes. Finally, we show that the transverse spatial structure of the interaction is characterised by the same mode decomposition.

Nitrogen vacancy (NV) centers in diamond have distinct promise as solid-state qubits. This is because of their large dipole moment, convenient level structure and very long room-temperature coherence times. In general, a combination of ion irradiation and subsequent annealing is used to create the centers, however for the rigorous demands of quantum computing all processes need to be optimized, and decoherence due to the residual damage caused by the implantation process itself must be mitigated. To that end we have studied photoluminescence (PL) from NV$^-$, NV$^0$ and GR1 centers formed by ion implantation of 2MeV He ions over a wide range of fluences. The sample was annealed at $600^{\circ}$C to minimize residual vacancy diffusion, allowing for the concurrent analysis of PL from NV centers and irradiation induced vacancies (GR1). We find non-monotic PL intensities with increasing ion fluence, monotonic increasing PL in NV$^0$/NV$^-$ and GR1/(NV$^0$ + NV$^1$) ratios, and increasing inhomogeneous broadening of the zero-phonon lines with increasing ion fluence. All these results shed important light on the optimal formation conditions for NV qubits. We apply our findings to an off-resonant photonic quantum memory scheme using vibronic sidebands

The extreme properties of diamond have led its use in a wide variety of applications from drilling for oil to ultra sharp knives for eye surgery. In the nanotechnology realm, diamond is being recognized as a material with great potential. For example, the extremely high modulus suggests that diamond could be used in Nano-Electro-Mechanical systems (NEMS) and quantum NEMS applications since diamond cantilevers will have higher oscillation frequencies than other materials. Furthermore diamond is chemically inert and biocompatible, and the surface can be functionalized which makes it attractive for potential nano-bio

A technique to measure the decoherence time of optical phonons in a solid is presented. Phonons are excited with a pair of time-delayed 80 fs near infrared pulses via spontaneous transient Raman scattering. The spectral fringe visibility of the resulting Raman pulse pair, as a function of time delay, is used to measure the phonon dephasing time. The method avoids the need to use either narrow band or few femtosecond pulses and is useful for low phonon excitations. The dephasing time of phonons created in bulk diamond is measured to be = 6.8 ps ͑⌬ = 1.56 cm −1 ͒.

We introduce a figure of merit for a quantum memory which measures the preservation of entanglement between a qubit stored in and retrieved from the memory and an auxiliary qubit. We consider a general quantum memory system consisting of a medium of two level absorbers, with the qubit to be stored encoded in a single photon. We derive an analytic expression for our figure of merit taking into account Gaussian fluctuations in the Hamiltonian parameters, which for example model inhomogeneous broadening and storage time dephasing. Finally we specialize to the case of an atomic quantum memory where fluctuations arise predominantly from Doppler broadening and motional dephasing.Comment: 5 pages, 3 figure