Microwave and optical transitions of rare-earth ions enable microwave-to-optical frequency transduction. This transduction is a coherent process; therefore, the narrow linewidths and long coherence times of rare-earth ions are crucial for achieving efficient frequency conversion. Particularly long coherence times can be achieved with small-spin materials, as unpaired electronic and nuclear spins introduce magnetic noise, serving as a decoherent source of the transitions. However, complete spin-free rare-earth materials cannot exist without charge compensation. Consequently, residual spins in existing rare-earth materials act as a bottleneck, limiting both their spin and optical coherence times. Rather than focusing on nearly spin-free materials, this thesis investigates the microwave and optical transitions of rare-earth ions in materials that are fully concentrated with electronic spins. Recent studies on rare-earth magnetic materials have demonstrated narrow optical linewidths resulting from magnetic ordering and a particularly strong coupling between microwave cavity modes and the collective excitations of rare-earth ions. Although these recent studies are noteworthy, the energy-level transitions, especially optical transitions, of rare-earth ions in magnetic materials remain largely unexamined. In this thesis, various spectroscopic studies are employed to characterise their transition properties and to develop a model of energy levels. The model presented is expected to be applicable to other rare-earth magnetic materials, thereby opening avenues for further investigation in this class of systems. Two types of rare-earth magnetic materials are investigated: neodymium gallate with a stoichiometric concentration of neodymium ions, and gadolinium vanadate doped with a low (ppm) concentration of erbium ions. Microwave and optical transmission spectroscopy are employed under externally applied magnetic fields to characterise the energy-state transitions of the rare-earth ions in both materials. The magnetic phases and corresponding spin configurations influence the observed spectra, making conventional approaches to spectral simulation inadequate. To address this challenge, mean field and magnon-coupled crystal-field models are developed in this thesis to predict magnon and optical transition spectra. These simulations exhibit good agreement with experimental results, allowing for the characterisation of transition properties. Following the characterisation of the material, a new transduction approach is introduced, developed, and implemented using doped rare-earth ions in a magnetic material. In this scheme, coherent conversion between microwave and optical modes is achieved by exciting an optical transition of the doped ions.
Microwave and optical transitions of rare-earth ions enable microwave-to-optical frequency transduction. This transduction is a coherent process; therefore, the narrow linewidths and long coherence times of rare-earth ions are crucial for achieving efficient frequency conversion. Particularly long coherence times can be achieved with small-spin materials, as unpaired electronic and nuclear spins introduce magnetic noise, serving as a decoherent source of the transitions. However, complete spin-free rare-earth materials cannot exist without charge compensation. Consequently, residual spins in existing rare-earth materials act as a bottleneck, limiting both their spin and optical coherence times. Rather than focusing on nearly spin-free materials, this thesis investigates the microwave and optical transitions of rare-earth ions in materials that are fully concentrated with electronic spins. Recent studies on rare-earth magnetic materials have demonstrated narrow optical linewidths resulting from magnetic ordering and a particularly strong coupling between microwave cavity modes and the collective excitations of rare-earth ions. Although these recent studies are noteworthy, the energy-level transitions, especially optical transitions, of rare-earth ions in magnetic materials remain largely unexamined. In this thesis, various spectroscopic studies are employed to characterise their transition properties and to develop a model of energy levels. The model presented is expected to be applicable to other rare-earth magnetic materials, thereby opening avenues for further investigation in this class of systems. Two types of rare-earth magnetic materials are investigated: neodymium gallate with a stoichiometric concentration of neodymium ions, and gadolinium vanadate doped with a low (ppm) concentration of erbium ions. Microwave and optical transmission spectroscopy are employed under externally applied magnetic fields to characterise the energy-state transitions of the rare-earth ions in both materials. The magnetic phases and corresponding spin configurations influence the observed spectra, making conventional approaches to spectral simulation inadequate. To address this challenge, mean field and magnon-coupled crystal-field models are developed in this thesis to predict magnon and optical transition spectra. These simulations exhibit good agreement with experimental results, allowing for the characterisation of transition properties. Following the characterisation of the material, a new transduction approach is introduced, developed, and implemented using doped rare-earth ions in a magnetic material. In this scheme, coherent conversion between microwave and optical modes is achieved by exciting an optical transition of the doped ions.
We characterise optical transitions of neodymium ions (Nd3+) in antiferromagnetic neodymium gallate (NdGaO3) with applied fields up to 3 T. The magnetic phase of this material has not previously been studied with the field along its magnetisation axis. The measured optical spectra indicate three magnetic phases -- antiferromagnetic, intermediate, and paramagnetic -- where the intermediate phase likely forms a different magnetic structure from typical spin-flop phases. The observed absorptions were classified into two distinct families of optical transitions: single-Nd and two-Nd absorptions. We demonstrate that the optical transitions in the antiferromagnetic and paramagnetic phases can be modelled using a standard single-ion crystal-field Hamiltonian that interacts with a mean magnetisation from the rest of the lattice, and we expand that model to encompass pairs of ions, explaining the origins of the two-Nd transitions. This study offers a deeper understanding of the optical transitions in rare-earth antiferromagnetic crystals, which have been recently attracting significant interest for microwave-to-optical quantum transduction, despite being relatively unexplored to date.
This thesis describes investigations of the use of cryogenically cooled rare-earth-ion-doped crystals for quantum information processing and quantum optics. Several aspects of the coherent interaction between light and rare-earth ions in solids are addressed. Quantum information science has given physicists new views of quantum mechanics. The transmission of quantum states has already found practical use and full scale quantum computers may one day perform computations and simulations that would be impossible on a conventional computer. The work presented in this thesis can be seen as a part of a broad effort to learn how to control and manipulate quantum mechanical systems, which will become necessary as science and technology continue to push ever deeper into the nanoscopic world. Coherent radiation, such as laser light, provides us with an ideal tool for these investigations and, along the way, we may also learn more about the quantum nature of light. Rare-earth ions in inorganic crystals have several unusual properties that are interesting for applications within quantum information science, including long coherence times and long-lived ground state sublevels that can be used for storage of quantum and classical information. As part of the work presented in this thesis, new materials have been investigated with respect to these properties, and ways to enhance the useful properties of the materials were explored. In one investigation, the lifetime of information stored in the ground state population distribution of Tm3 ions in YAG was shown to increase by several orders of magnitude with the application of a magnetic field. It is demonstrated how the optical inhomogeneous absorption profile can be prepared, so that the light only interacts with a selected group of ions, absorbing on a specific transition. Narrow absorbing structures, with widths approaching the optical homogeneous linewidth, have been prepared with no absorption in the surrounding spectral interval. This thesis addresses the use of such structures as hardware for quantum bits. Tailored pulses, capable of inducing controlled changes in the quantum states of the ions (qubits), even in the presence of unknown variations of coupling strengths and frequencies, have been realised experimentally and used for multiple transfer of ions between energy levels. Ion-ion interactions, which can be used for performing quantum logic operations, have been investigated in some detail. Techniques for selecting strongly interacting ions, by transferring weakly interacting ions to auxiliary states, have been demonstrated. A scheme for storing the quantum state of light in a solid, using photon-echo-like techniques, is proposed and analysed. In the proposed scheme, an optical wave packet is absorbed and subsequently re-emitted by an inhomogeneous absorption profile, which is tailored and externally controlled by the application of an electric field Additionally, an accumulated photon echo experiment has been performed using faint optical pulses. The experiment can be viewed as a demonstration of delayed self-interference of a single photon and as a demonstration of how a single photon can act as two of the fields in a photon echo process.
Elucidating magnetic structure with optical dopants: erbium-doped Gd2SiO5
The narrowness of the optical transitions of rare-earth-ion dopants makes them highly sensitive probes of their environment. We measured the optical transitions Er3+ dopants to determine the previously unknown magnetic ordering of Gd2SiO5 -- a promising host for quantum applications of rare-earth dopants. By measuring the transitions' magnetic-field dependence we determined an antiferromagnetic ordering with spins oriented along or slightly canted from the crystal's a∗ axis. The optical transitions are narrower than the coupling to gadolinium spins revealing information about the coupling strengths. We further optically measured a Néel temperature of 1.86±0.01stat.±0.07syst. K, and assembled a phase diagram in applied field and temperature showcasing a triple point where two gadolinium sites order semi-independently from each other. At high applied field the erbium dopants show long optical coherence times up to 0.4 ms at 3 T; at low fields these are probably limited by three low-frequency magnon modes below 10 GHz, observed directly. This study can be used to benchmark a method of magnetic structure determination.
When doped into solid state transparent crystals, rare-earth ions can have optically excited states with milliseconds coherence time and up to six hours coherence time for hyperfine levels after being cooled down to liquid helium temperature. This long coherence property makes them unique as solid state material and attractive for quantum information applications.The rare-earth ions have narrow homogeneous linewidths on the order of ~ kHz. When doped into a crystal, the lattice structure is slightly distorted due to the size mismatch between the dopant and the host ions, resulting in slight differences in the local crystal fields at the dopant sites. Therefore, the resonance frequencies of the rare-earth ions are shifted relatively, resulting in an inhomogeneously broadened absorption profile, typically on the order of a few GHz. This provides the possibility of addressing each group of ions individually and engineering the absorption profile for different purposes by optical pumping using a narrow linewidth laser, and makes rare-earth-ion-doped crystals suitable for ensemble based quantum memories.Quantum memories are vital components for developing longdistance quantum communication. Part of this thesis project focused on making quantum memories with high efficiency and long storage time, especially using materials with low optical depth. To achieve this goal, a low finesse, unsymmetrical cavity was employed and experiments were carried out at (or close to) the impedance matched condition. Atomic frequency comb (AFC) protocol proposed for such an inhomogeneously broadened system was used to store coherent light for a certain time. 56% overall efficiency was achieved, and the main limiting factor for reaching even higher efficiency was the inefficient coupling between incoming light and the cavity mode. Other possible loss mechanisms were analyzed as well.Long-time, on-demand, quantum memory experiments were conducted with the help of two efficient radio-frequency rephasing pulses. Storage time was extended from microseconds to milliseconds after compensating (most of) the residual earth magnetic field in the lab. The opportunities and challenges of combing the cavity assistant quantum memory and the long time, on demand quantum memory were analyzed and possible solutions were proposed. Another part of the thesis project involves slow light-based applications in rare-earth-ion-doped crystals. The strong slow light effect at the presence a spectral hole is due to the fact that the light interacts with the absorbing ions outside the spectral hole off-resonantly, and most of the light energy is stored inside the ions as a polarization. For example, with a group velocity of 300 km/s, 99.9% of the pulse energy is stored in the ions when the pulse propagates inside the crystal. The slower the light propagates, the more energy is stored inside the medium. Based on this, a frequency shifter that is capable of shifting the light frequency of ± 4 MHz was demonstrated, and frequency shift up to GHz was proposed. Group velocity control by a factor of 20 and pulse compression in time by a factor of 2 were also demonstrated. The frequency shift and group velocity of the light are solely controlled by the external electric field, which makes them ideal for weak light situation. The unique property of such a frequency shifter and group velocity controller is that they could be made to accept light from an arbitrary incoming angle and polarization, for example, scattered light.
This thesis presents a spectroscopic study of Pr3+ ions in a novel passive waveguide architecture. To make this structure, the high refractive glass TeO2 was selected as the thin film and it was deposited on a Pr3+:Y2SiO5 crystal. In this waveguide, the 3H4 to 1D2 transition of Pr3+ ions were probed by the optical evanescent field extending into the substrate. The main concern in assessing the suitability of this material for quantum information applications was ensuring that the coherence properties of rare-earth ions, making them suitable for quantum information purposes, are preserved in this architecture. After which, to make low loss devices with these waveguides, efficient coupling techniques had to be developed. To prove that the coherence properties of the rare-earth ion doped crystal were preserved, the critical parameters of inhomogeneous linewidth, the absorption of the ions, the coherence time and spin lifetimes of the Pr3+ ions were studied. The inhomogeneous linewidth of evanescent coupled ions was about 10.0 GHz, which was consistent with the linewidth of bulk samples with the same Pr3+ doping concentration (Hedges, 2011). The absorption due to the evanescent coupling was 9.38 dB, approximately 90% of what was expected with respect to the bulk crystal with the same doping concentration. Therefore, despite using the evanescent field, the absorption is high enough for quantum memory applications. An optical coherence time of about 121 microseconds was measured, which corresponded to a homogeneous linewidth of about 2.6 kHz. This is very close to bulk sample measurements of 111 microseconds, with the same temperature and doping concentration (R. W. Equall, 1995). The spin state lifetime observed was about 9.8 s, which is also very close to the bulk sample measurement of 8.67 s (Mieth, 2016). Initial Stark shifting experiments were performed to determine whether the active ions in the substrate of the passive waveguides could be electrically controlled by applying a small voltage to electrodes on the thin film. In these experiments with a voltage change of 100 mV, the measured holewidth broadening was increasing about 0.55 MHz, which was similar to the calculated values of 0.45 MHz. The Stark coefficient for site 1 was 51.6 kHzcm/V along the D2 axis of the crystal (site 1 will be explained in Section 4.3). (F.R. Graf, 1997). Prism coupling and grating coupling were used to couple light to the ions in the substrate. Prism coupling is an easy and quick method to couple light into a waveguide and observe the properties of the system. However, grating coupling is much more practical when moving towards building a device using this method. The measurements described above indicated that the properties of ions interacting with the evanescent tail of the waveguide mode were consistent with those of bulk ions. This investigation also showed that depositing a glass thin film on a rare-earth ion doped crystal was not affecting the good coherence properties of the substrate. These results establish the foundation for large, integrated, controllable and high performance rare earth ion quantum waveguide systems.
Quantum light-matter interfaces that can reversibly map quantum information between photons and atoms are essential for building future quantum networks. Crystals doped with rare-earth ions (REIs) are an attractive solid-state platform for such light-matter interfaces due to their exceptional optical and spin coherence properties at cryogenic temperatures. Building scalable REI-based technology has proven to be challenging due to the inherently weak coupling of REIs with light. This thesis explores the integration of REIs with nanophotonic resonators to overcome this weak light-matter interaction and enable efficient, scalable quantum light-matter interfaces. Specifically, this work focuses on the development of quantum nanophotonics with ytterbium in yttrium orthovanadate. This thesis begins with an introduction to a nanophotonic platform based on photonic crystal cavities fabricated directly in rare-earth host materials and highlights the initial successes of this platform with neodymium-doped materials. This motivates an examination of the optical and spin coherence properties of 171Yb:YVO4, a REI material that was previously unexplored for quantum technology applications. This material is found to have strong optical transitions compared to other REI-doped materials, a simple energy level structure, and long optical and spin coherence lifetimes. The focus then turns to the detection and coherent manipulation of single ytterbium ions coupled to nanophotonic cavities. The Purcell-enhancement in these cavities enables efficient optical detection and spin initialization of individual ytterbium ions. We identify ions corresponding to different isotopes of ytterbium and show that the coupling of electron and nuclear spin in ytterbium-171 at zero-field gives rise to strong electron-spin-like transitions that are first-order insensitive to magnetic field fluctuations. This allows for coherent microwave control and the observation of long spin coherence lifetimes at temperatures up to 1 K. We then make use of the optical selection rules and energy structure of 171Yb:YVO4 to demonstrate high-fidelity single-shot optical readout of the spin state. These results establish nanophotonic devices in 171Yb:YVO4 as a promising platform for solid-state quantum light-matter interfaces.