We researched the realization of novel optical functions of glass by combining an external electromagnetic field induced electronic structure and rare-earth-ions. We reviewed the phenomena, mechanisms, and the applications of photostimulated luminescence induced by X-ray, long-lasting phosphorescence by ultra-violet light, space-selective manipulation of the valence state of rare-earth-ion, and the formation of rare-earth-ion-doped optical waveguide for light amplification by a focused infrared femtosecond laser. The proposed concept will lead to a new possibility in the realization of novel optical functions for rare-earth-ion-doped glasses.
We researched the realization of novel optical functions of glass by combining an external electromagnetic field induced electronic structure and rare-earth-ions. We reviewed the phenomena, mechanisms, and the applications of photostimulated luminescence induced by X-ray, long-lasting phosphorescence by ultra-violet light, space-selective manipulation of the valence state of rare-earth-ion, and the formation of rare-earth-ion-doped optical waveguide for light amplification by a focused infrared femtosecond laser. The proposed concept will lead to a new possibility in the realization of novel optical functions for rare-earth-ion-doped glasses.
Abstract Controlling the up-conversion luminescence of rare-earth ions in real-time, in a dynamical and reversible manner, is very important for their application in laser sources, fiber-optic communications, light-emitting diodes, color displays and biological systems. In previous studies, the up-conversion luminescence control mainly focused on the weak femtosecond laser field. Here, we further extend this control behavior from weak to intermediate femtosecond laser fields. In this work, we experimentally and theoretically demonstrate that the up-conversion luminescence in Dy 3+ ion doped glass can be artificially controlled by a π phase step modulation, but the up-conversion luminescence control behavior will be affected by the femtosecond laser intensity, and the up-conversion luminescence is suppressed by lower laser intensity while enhanced by higher laser intensity. We establish a new theoretical model (i.e. the fourth-order perturbation theory) to explain the physical control mechanism by considering the two- and four-photon absorption processes, and the theoretical results show that the relative weight of four-photon absorption in the whole excitation process will increase with the increase in laser intensity, and the interference between two- and four-photon absorptions results in up-conversion luminescence control modulation under different laser intensities. These theoretical and experimental works can provide a new method to control and understand up-conversion luminescence in rare-earth ions, and also may open a new opportunity to the related application areas of rare-earth ions.
Research and development of nanoscale luminescent and laser materials are part of the rapidly advancing nanoscience and nanotechnology. Because of unique spectroscopic properties and luminescent dynamics of f-electron states, doping luminescent rare earth ions into nano-hosts has been demonstrated as an optimistic approach to developing highly efficient and stable nanophosphors for various applications. In this article, we review the most recent progress in spectroscopic measurements of rare earth ion-activated low-dimensional nanostructures including nanolayers, core-shells, nanowires, nanotubes, and nanodisks. Among a large volume of work reported in the literature on many members of the rare earth series including Ce3+, Pr3+, Nd3+, Eu3+, and Er3+, we focus on recent findings in the spectroscopic and luminescence properties of Eu3+ doped nanolayers, core-shells, and nanotubes, because Eu3+ ions have been extensively studied and widely used as an ideal probe for fundamental understanding of nano-phenomena. Specifically, the dependence of the optical properties of rare earth ions on nanostructures is discussed in detail.
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.
This thesis reports experiments and theory on intrinsic mirrorless bistability in the luminescence of ytterbium-doped crystals and glasses. The main results are the observation of intrinsically bistable luminescence at room temperature and chromatic switching at low temperature, reported here for the first time. The nonlinear dynamics responsible for these optical phenomena are shown to arise from ion-ion interactions controlled by the application of resonant electromagnetic fields. On the theoretical side, the classical Lorentz local field correction is shown to be the lowest order term of radiation-driven correlation contributions to local polarization which arise from inter-ion coherences and cooperative relaxation and frequency shifts beyond the dynamic shift are predicted. The nonlinear Maxwell-Bloch equations are extended to describe energy transfer between different species of ions predicting bistability in excited state populations which then emit bistable luminescence as a consequence, and an intensity dependent transfer rate is predicted. Diffusive excitation migration in space is also explored as a possible mechanism for generating multiple instabilities, but is not predicted to give rise to hysteresis loops by itself. On the experimental side, original observations of intrinsic optical switching and hysteresis are reported in the luminescence of Yb:CsCdBr 3 and Yb, Tm:glass. Evidence of cross-coupling between different impurities is also presented, together with spectroscopic details of intrinsic chromatic switching between different luminescent transitions of the acceptor species in Yb, Er:CsCdBr3 excited at the infrared Yb resonance wavelength. Conclusive spectroscopic evidence that excludes thermal effects as responsible for low temperature intrinsic switching is also presented. Room temperature intrinsic optical switching and hysteresis are reported for the first time in bulk Yb,Tm:glass samples. Switching, hysteresis, and clamping of laser output from waveguide channels fabricated in the glass material are also reported and indicate fundamental design limitations for compact optical amplifiers and oscillators.
We report the experimental observation of a slow-light information conversion via electromagnetically induced transparency (EIT) in a rare-earth-ion-doped solid. Under the EIT-based slow-light regime, by manipulating the spectrum of the control fields, the slowed light pulse is transformed into two different frequency-spatial channels. The pulse shapes and energies in two output channels are further studied. This slow-light information conversion can be used as a controllable frequency-spatial multiplexing of the quantum state of the optical field and will be important in information processing and all-optical networks.