Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

QUANTUM COUNTER ACTION IN DIVALENT RARE EARTH SYSTEMS

M. R. Brown, W. A. Shand, James M. Williams

Published Jul 1, 1969• 0 citations
OpenAlex

Abstract

Abstract : Quantum counter action has been observed in divalent rare earth doped ions lattices. The report presents the experimental work that has been done on Sm(2+) and Tm(2+) singly doped and Sm(2+) : Tm(2+) double doped systems in order to investigate the nature and efficiency of the schemes. The results show that while these systems are more efficient per ion than the trivalent rare earth doped systems the lower concentrations possible bring the overall efficiency back to the same level. (Author)

Related papers

7C7 - Infrared quantum counter action in rare earth doped fluoride lattices

M. Brown, W. A. Shand

This paper reviews the results of a program of experimental work on infrared quantum counter action in trivalent rare earth doped CaF2, SrF2, BaF2, and LaF3lattices. The action has been found in eight of the nine possible ions that could give an output in the visible region. While the strengths of the various schemes at a 1 percent doping level are consistant with a low concentration theory, the strengths of the schemes at a 10 percent doping level indicate that there are ion-ion interactions influencing the systems. These ion-ion couplings are so effective that three photon addition schemes have been identified.

IEEE Journal of Quantum Electronics•Aug 1, 1966•7 citations

SOME EXPERIMENTS ON Er(3+)DOPED LiYF4,

M. R. Brown, K. J. Roots, W. A. Shand

Abstract : Previous work on the infrared quantum counter action in Er3+ doped SrF2 showed that it was possible to increase the efficiency of the action by codoping with a second rare earth ion. This report covers the work done on the Er3+ doped LiYF4 and Er3+: Yb3+ doped LiYF4 system to evaluate the energy levels of the Er3+ in a site that does not require charge compensation and the increase of efficiency that comes with codoping with Yb3+. The results show that the positions of the energy levels are substantially unchanged in moving from one lattice to another and an increase in efficiency of the action, of the order, forty times can be achieved with a composition in the region of 2% Er3+: 18% Yb3+ doped LiYF4. (Author)

•Jul 1, 1969•0 citations

Quantum counter action in Er3+ : Yb3+ doped LiYF4

M R Brown, W. A. Shand

This paper considers the mechanisms whereby the addition of Yb 3+ enhances the efficiency of quantum counter action in Er 3+ doped LiYF 4 . The particular scheme chosen for this investigation is the doubling scheme in which two photons of wavelength close to 9800 Å excite green fluorescence from the Er 3+ ion. The important factors which have been identified are that the influence of an increase of Yb 3+ concentration on the quantum efficiency of the 4 S 3/2 to 4 I 15/2 fluorescence is very much less than an equivalent increase in the Er 3+ concentration, the absorption coefficient of the Yb 3+ in the 9800 Å region is over an order of magnitude larger than that for Er 3+ and the efficiency of the transfer of energy from Yb 3+ to Er 3+ is sufficiently high to ensure the energy absorbed by the Yb 3+ is transferred to the Er 3+ . The optimum concentration has been found to be in the region of 2% Er 3+ : 18% Yb 3+ doped LiYF 4 .

Journal of Physics C Solid State Physics•Nov 1, 1969•3 citations

Laser induced quantum counter action of trivalent rare-earth ions in lanthanide halide hosts

D. E. Cox

•Jan 1, 1974•0 citations

Recent Advances in Rare Earth Doped Inorganic Crystalline Materials for Quantum Information Processing

Nathalie Kunkel, Philippe Goldner

Since quantum information technologies are expected to offer communication security and high computational capacities, research in the field is currently attracting a lot of attention. Among the materials studied so far, rare earth doped inorganic insulators are one of the most promising. With the different available trivalent rare earth ions, the visible and the IR range including the telecom wavelength at 1.5 μm can be covered. Transitions are usually narrow, and at low temperatures, long optical and spin coherence times can often be observed. Investigations using bulk single crystals have already led to many promising results. Recently, spectroscopic studies have been extended to other forms of inorganic materials, such as transparent ceramics, thin films, and nanoparticles for single rare‐earth qubits. Progress in these areas is expected to offer many new possibilities for the design of quantum light‐matter interfaces and scalable quantum memories and processors.

Zeitschrift für anorganische und allgemeine Chemie•Dec 6, 2017•54 citations

Quantum computing with naturally trapped sub-nanometre-spaced ions

Lars Rippe

The main aim of this work, was to lay the foundations for the experimental realisation of a quantum mechanical controlled NOT gate in rare-earth-metal-ion-doped crystals. Small amounts of rare-earth elements, added during the growth of some inorganic crystals, will become substituted into the crystal lattice as trivalent ions. The trivalent rare-earth-metal ions between cerium, with atomic number 58, and ytterbium, with atomic number 70, have a partly filled 4f shell, which does not extend spatially outside the full 5s and 5p shells. The 4f vacancies make electronic inner shell transitions possible between spectroscopic 4f terms. Some of these optical transitions have coherence times of the order of milliseconds, when the crystals are cooled down to ~ 4 K. There are several reasons for these extraordinary coherence times, which are approximately 8 orders of magnitude greater than those typical for electronic transitions in solids. The most important one is the cage-like shield which the outer 5s and 5p shells provide for the 4f electrons. Furthermore, since these ions are naturally trapped inside the crystal lattice there is no Doppler broadening of the line-width. The coherence properties of these optical transitions is one of the features that makes these materials attractive for use as a solid-state platform for quantum computing, using these ions as qubits. Another appealing characteristic is the fact that different ions have different optical resonance frequencies, which means that ions belonging to different qubits, which only have nm separation, can still be addressed separately by using different laser frequencies. Since the inter-ion spacing is so small, it is possible to make two ions interact strongly, although they are well shielded, through a permanent dipole-dipole interaction. This interaction can be turned on and off by switching between two different ways of encoding the qubit, a most useful feature. When the qubit is represented as a superposition between two ground state hyperfine levels, the interaction is turned off. The interaction is turned on selectively by transferring this superposition to the optical transition with a pi-pulse, for the specific ions that are to interact. This thesis describes how peaks of ions, absorbing on a single transition, residing in spectral pits with no other ions, have been isolated. It is shown how these ions can be coherently transferred between hyperfine levels via the optically excited state, how the interaction between such peaks of ions representing qubits can be turned on and off, and how subgroups of ions with strong interaction can be distilled out. All the work described here has been performed using the ensemble approach. The ensemble approach will, however, be difficult to scale up to large numbers of qubits. A method employing a single ion in each qubit, using a specialised ion for readout, has therefore also been proposed. The rare-earth-metal-ion-based quantum computing experiments require a laser with coherence properties which at least match those of the material. To this end a frequency stabilisation system was developed for a dye laser. This system uses a transient spectral hole in a rare-earth-metal-ion-doped crystal, of the same kind that is used in the experiments, as frequency reference, and is to the authors knowledge the first demonstration of locking a dye laser to a spectral hole. This system provides a line-width of 1 kHz on a 10 microseconds timescale and a frequency drift below 1 kHz/s.

•Jan 1, 2006•7 citations
Abstract : Quantum counter action has been observed in divalent rare earth doped ions lattices. The report presents the experimental work that has been done on Sm(2+) and Tm(2+) singly doped and Sm(2+) : Tm(2+) double doped systems in order to investigate the nature and efficiency of the schemes. The results show that while these systems are more efficient per ion than the trivalent rare earth doped systems the lower concentrations possible bring the overall efficiency back to the same level. (Author)
This paper reviews the results of a program of experimental work on infrared quantum counter action in trivalent rare earth doped CaF2, SrF2, BaF2, and LaF3lattices. The action has been found in eight of the nine possible ions that could give an output in the visible region. While the strengths of the various schemes at a 1 percent doping level are consistant with a low concentration theory, the strengths of the schemes at a 10 percent doping level indicate that there are ion-ion interactions influencing the systems. These ion-ion couplings are so effective that three photon addition schemes have been identified.
Abstract : Previous work on the infrared quantum counter action in Er3+ doped SrF2 showed that it was possible to increase the efficiency of the action by codoping with a second rare earth ion. This report covers the work done on the Er3+ doped LiYF4 and Er3+: Yb3+ doped LiYF4 system to evaluate the energy levels of the Er3+ in a site that does not require charge compensation and the increase of efficiency that comes with codoping with Yb3+. The results show that the positions of the energy levels are substantially unchanged in moving from one lattice to another and an increase in efficiency of the action, of the order, forty times can be achieved with a composition in the region of 2% Er3+: 18% Yb3+ doped LiYF4. (Author)
This paper considers the mechanisms whereby the addition of Yb 3+ enhances the efficiency of quantum counter action in Er 3+ doped LiYF 4 . The particular scheme chosen for this investigation is the doubling scheme in which two photons of wavelength close to 9800 Å excite green fluorescence from the Er 3+ ion. The important factors which have been identified are that the influence of an increase of Yb 3+ concentration on the quantum efficiency of the 4 S 3/2 to 4 I 15/2 fluorescence is very much less than an equivalent increase in the Er 3+ concentration, the absorption coefficient of the Yb 3+ in the 9800 Å region is over an order of magnitude larger than that for Er 3+ and the efficiency of the transfer of energy from Yb 3+ to Er 3+ is sufficiently high to ensure the energy absorbed by the Yb 3+ is transferred to the Er 3+ . The optimum concentration has been found to be in the region of 2% Er 3+ : 18% Yb 3+ doped LiYF 4 .
Since quantum information technologies are expected to offer communication security and high computational capacities, research in the field is currently attracting a lot of attention. Among the materials studied so far, rare earth doped inorganic insulators are one of the most promising. With the different available trivalent rare earth ions, the visible and the IR range including the telecom wavelength at 1.5 μm can be covered. Transitions are usually narrow, and at low temperatures, long optical and spin coherence times can often be observed. Investigations using bulk single crystals have already led to many promising results. Recently, spectroscopic studies have been extended to other forms of inorganic materials, such as transparent ceramics, thin films, and nanoparticles for single rare‐earth qubits. Progress in these areas is expected to offer many new possibilities for the design of quantum light‐matter interfaces and scalable quantum memories and processors.
The main aim of this work, was to lay the foundations for the experimental realisation of a quantum mechanical controlled NOT gate in rare-earth-metal-ion-doped crystals. Small amounts of rare-earth elements, added during the growth of some inorganic crystals, will become substituted into the crystal lattice as trivalent ions. The trivalent rare-earth-metal ions between cerium, with atomic number 58, and ytterbium, with atomic number 70, have a partly filled 4f shell, which does not extend spatially outside the full 5s and 5p shells. The 4f vacancies make electronic inner shell transitions possible between spectroscopic 4f terms. Some of these optical transitions have coherence times of the order of milliseconds, when the crystals are cooled down to ~ 4 K. There are several reasons for these extraordinary coherence times, which are approximately 8 orders of magnitude greater than those typical for electronic transitions in solids. The most important one is the cage-like shield which the outer 5s and 5p shells provide for the 4f electrons. Furthermore, since these ions are naturally trapped inside the crystal lattice there is no Doppler broadening of the line-width. The coherence properties of these optical transitions is one of the features that makes these materials attractive for use as a solid-state platform for quantum computing, using these ions as qubits. Another appealing characteristic is the fact that different ions have different optical resonance frequencies, which means that ions belonging to different qubits, which only have nm separation, can still be addressed separately by using different laser frequencies. Since the inter-ion spacing is so small, it is possible to make two ions interact strongly, although they are well shielded, through a permanent dipole-dipole interaction. This interaction can be turned on and off by switching between two different ways of encoding the qubit, a most useful feature. When the qubit is represented as a superposition between two ground state hyperfine levels, the interaction is turned off. The interaction is turned on selectively by transferring this superposition to the optical transition with a pi-pulse, for the specific ions that are to interact. This thesis describes how peaks of ions, absorbing on a single transition, residing in spectral pits with no other ions, have been isolated. It is shown how these ions can be coherently transferred between hyperfine levels via the optically excited state, how the interaction between such peaks of ions representing qubits can be turned on and off, and how subgroups of ions with strong interaction can be distilled out. All the work described here has been performed using the ensemble approach. The ensemble approach will, however, be difficult to scale up to large numbers of qubits. A method employing a single ion in each qubit, using a specialised ion for readout, has therefore also been proposed. The rare-earth-metal-ion-based quantum computing experiments require a laser with coherence properties which at least match those of the material. To this end a frequency stabilisation system was developed for a dye laser. This system uses a transient spectral hole in a rare-earth-metal-ion-doped crystal, of the same kind that is used in the experiments, as frequency reference, and is to the authors knowledge the first demonstration of locking a dye laser to a spectral hole. This system provides a line-width of 1 kHz on a 10 microseconds timescale and a frequency drift below 1 kHz/s.