WO2015015172A1 - Détecteur sensible - Google Patents

Détecteur sensible Download PDF

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Publication number
WO2015015172A1
WO2015015172A1 PCT/GB2014/052289 GB2014052289W WO2015015172A1 WO 2015015172 A1 WO2015015172 A1 WO 2015015172A1 GB 2014052289 W GB2014052289 W GB 2014052289W WO 2015015172 A1 WO2015015172 A1 WO 2015015172A1
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WO
WIPO (PCT)
Prior art keywords
colour
centre
sample
centres
detector
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PCT/GB2014/052289
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English (en)
Inventor
Gavin William MORLEY
Mark Edward Newton
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The University Of Warwick
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Publication of WO2015015172A1 publication Critical patent/WO2015015172A1/fr

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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N24/00—Investigating or analyzing materials by the use of nuclear magnetic resonance, electron paramagnetic resonance or other spin effects
    • G01N24/08—Investigating or analyzing materials by the use of nuclear magnetic resonance, electron paramagnetic resonance or other spin effects by using nuclear magnetic resonance
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N24/00—Investigating or analyzing materials by the use of nuclear magnetic resonance, electron paramagnetic resonance or other spin effects
    • G01N24/08—Investigating or analyzing materials by the use of nuclear magnetic resonance, electron paramagnetic resonance or other spin effects by using nuclear magnetic resonance
    • G01N24/087—Structure determination of a chemical compound, e.g. of a biomolecule such as a protein
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00—Arrangements or instruments for measuring magnetic variables
    • G01R33/20—Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/60—Arrangements or instruments for measuring magnetic variables involving magnetic resonance using electron paramagnetic resonance
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00—Arrangements or instruments for measuring magnetic variables
    • G01R33/20—Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/62—Arrangements or instruments for measuring magnetic variables involving magnetic resonance using double resonance

Definitions

  • the present invention relates to a detector for electromagnetic radiation and/or EPR/NMR (electron paramagnetic resonance/nuclear magnetic resonance), which exploits the electron-spin- dependent fluorescence of a colour centre in a solid.
  • the detector may be used in a wide range of applications, including as part of a communication system or as part of an imaging, EPR or NMR system.
  • the detectors can be selectively tuned to be sensitive to frequencies in the range of 1 Hz to lO THz.
  • Examples of devices requiring such detectors include mobile phones, mobile phone base stations, radar (including weather radar), WiFi devices, cordless telephones, wireless headphones, video senders, walkie talkies, Bluetooth, telemetry, GPS, astronomy and imaging.
  • Detectors for performing single-molecule NMR experiments need to be highly sensitive to the magnetic field originating from individual atoms of the molecule under study. It has been proposed [23, 24] that the NMR of single molecules could be studied by using a single nitrogen vacancy (NV ) centre in diamond as a scanning magnetometer. In the proposed methodology the scanning is performed at low magnetic field, which involves considerable spectral overlap between different NMR resonances. This is addressed by scanning the magnetometer around in real space so that it sequentially visits each nucleus. However, the scanning procedure is slow and nuclei in the middle of a large molecule are inaccessible to the magnetometer.
  • NV nitrogen vacancy
  • a detector comprising: a substrate arranged to receive an input radiation to be detected and comprising a colour centre of a type that exhibits electron-spin-dependent fluorescence; and a spin measurement section for probing the spin state of the colour centre using fluorescence, thereby detecting input radiation that is such as to change the spin state of the colour centre.
  • the present invention thus exploits the fact that certain colour centres in solids exhibit electron-spin-dependent fluorescence at relatively high frequencies (for example at optical frequencies), and that electromagnetic radiation with a lower frequency (for example lower than optical frequencies, for example microwave frequencies) can flip these spins via magnetic resonance, to provide a practical device that is capable of sensitively detecting the presence of the lower frequency electromagnetic radiation. It is generally the case that higher frequency photons can be detected more sensitively than lower frequency photons, so converting the lower frequency input photons to higher frequency ones tends to increase the sensitivity with which they can be detected. In the case where the higher frequency photons are optical photons, for example, it is well known that there are a wide variety of devices capable of detecting optical photons with very high sensitivity.
  • the frequency sensitivity of the detector can be tuned by applying an appropriate magnetic field to the colour centres. The magnetic field changes the separation between energy levels associated with different electron spin states, which results in a change in the frequency or frequencies of magnetic resonance.
  • the spin state of an NV " centre in diamond for example can be changed by a single microwave photon, which can then be detected using an optical detector due to the spin-dependent fluorescence of the NV " centre. It is relatively routine to measure single optical photons, whereas single microwave photons cannot currently be detected with room temperature equipment because the energy of a microwave photon is over 100,000 times less than that of a single optical photon. Single microwave photons can be detected with advanced equipment based on superconducting electronics, but this requires cooling to liquid helium temperature of 4K (or below) which is impractical for large- scale commercial applications.
  • a detector according to an embodiment of the present invention using for example an NV " centre in diamond, can work efficiently at room temperature (and pressure).
  • the detector is used in a communication device, such as a mobile phone or mobile phone base station.
  • a communication device such as a mobile phone or mobile phone base station.
  • Frequencies currently used most commonly in this context are around 0.9 - 2 GHz.
  • the use of the detector in the base-station could greatly reduce the amount of power that a mobile phone needs to transmit, due to its increased sensitivity, thus reducing the power consumption of the device.
  • the extra detection sensitivity would also allow more data to be transmitted.
  • the detector is used to detect the radiation absorbed or emitted in a magnetic resonance experiment.
  • NMR nuclear magnetic resonance
  • EPR electron paramagnetic resonance
  • the detector can be tuned to be sensitive to these frequencies by appropriate application of an external magnetic field.
  • the detector is used in a radar (including weather radar), WiFi, cordless telephones, wireless headphones, video senders, walkie talkies, Bluetooth, telemetry, GPS, astronomy and imaging.
  • an apparatus for carrying out nuclear magnetic resonance comprising: a magnet configured to generate a magnetic field of equal to or greater than 5T in a test region of the magnet; and a probe comprising a sample receiver for receiving a sample, the probe being insertable into the magnet so as to position the sample receiver in the test region, wherein the probe comprises: a substrate comprising a colour centre of a type that exhibits electron-spin-dependent fluorescence, the colour centre being positioned so as to be directly adjacent in use to a sample in the sample receiver; a first coupling system for directing first electromagnetic radiation to the colour centre to control the electron spins of the colour centre using electron paramagnetic resonance and a second coupling system for directing second electromagnetic radiation to the sample in order to control the nuclear spins of the sample using nuclear magnetic resonance; and a third coupling system for directing third electromagnetic radiation to and from the colour centre in order to measure a change in the fluorescence of the colour centre resulting from a contribution to the magnetic field at the colour
  • colour centres are used as the basis for sensitive magnetometers in a high field NMR system.
  • the colour centres are used for single-molecule NMR.
  • a plurality of the colour centres are used to simultaneously probe different molecules in a sample of many molecules which may be identical. The different identical molecules will be oriented differently with respect to their respective detectors, so different parts of the molecule will be studied by each detector. This approach greatly increases the throughput of single-molecule NMR experiments.
  • Figure 1 depicts an example configuration in which microwave input radiation is directed to a substrate containing colour centres and the resulting optical fluorescence measured
  • Figure 2 depicts an alternative example configuration in which a substrate contains a plurality of the colour centres and a branched system of wires for directing input radiation to each of the colour centres;
  • Figure 3 depicts an example of a resonator for focusing input radiation onto a colour centre
  • Figure 4 depicts an example of a sample receiver comprising a plurality of colour centres and associated optical fibres for performing fluorescence measurements.
  • a detector in the specific example shown in Figure 1, has a substrate 4, a coupling device 6 and a spin measurement section 8.
  • the substrate 4 comprises a plurality of colour centres that are each of a type that exhibits electron-spin-dependent fluorescence.
  • a substrate may be provided that has only one colour centre or a plurality of different substrates may be provided that each comprise one or a plurality of colour centres.
  • the colour centres may all be of the same type or some or all of them may be of different types.
  • the coupling device 6 is configured to direct an input radiation beam to be detected to the colour centres in the substrate 4.
  • the coupling device 6 may comprise a waveguide, an antenna, a resonator, one or more reflectors, or any combination of these, for example.
  • a coupling device 6 is not provided, with the substrate 4 being instead directly exposed to the input radiation.
  • the spin measurement section 8 is configured to output a measure of the phase and/or intensity and/or frequency of the input radiation, based on the fluorescence.
  • the spin measurement section 8 is configured to output a measure of the phase and/or intensity and/or frequency as a function of time. The output may be provided for example by measuring the rate at which spins are flipped in a given colour centre or in a plurality of colour centres, for example.
  • the frequency could be measured by a) having different colour centres which undergo EPR at different frequencies and/or b) by applying different magnetic fields to tune the EPR resonant frequency of the colour centres.
  • the different magnetic fields could be applied sequentially to one or more colour centres and/or the tuning magnetic fields could be kept constant in time but chosen to be different for different colour centres.
  • the amplitude of the signal could be detected by observing the nutation rate (Rabi oscillation frequency) of the colour centre spin(s). The intensity can be calculated from the amplitude.
  • the phase of the signal could be detected by measuring the signal amplitude relative to the phase of a reference signal applied to the colour centres and using standard methods of phase-sensitive detection [David M Pozar, Microwave Engineering, John Wiley & Sons; 4th Edition (2011)].
  • a magnetic field control system 15 is provided for controlling the magnetic field in the region of the colour centre or centres to control the absorption spectrum (i.e. the magnetic resonance frequencies) of the colour centre or centres.
  • the magnetic field control system may be used to make the detector sensitive to one or more frequencies in the range of 1 Hz to lOTHz, for example.
  • the detector is used as part of a communication apparatus.
  • the detector may further comprise a demodulator 17 for receiving the output from the spin measurement section and extracting therefrom information that was modulated onto the input radiation.
  • the substrate 4 is provided in the form of a wafer, which has a thickness in the direction parallel to the input direction of the radiation that is several orders of magnitude smaller than the dimensions of the substrate perpendicular to the direction of incidence.
  • This geometry tends to increase the chance that one of the photons to be detected hits the detector without making it unduly difficult for optical photons to enter and leave the substrate (for the purposes of measuring the fluorescence - see below).
  • other geometries of substrate may be used.
  • the spin measurement section 8 comprises an input radiation source 10 for directing input radiation 12 for fluorescence onto the substrate 4 and detectors 14 for detecting the resultant fluorescence.
  • fluorescent photons emerge in all directions so conventional optics such as mirrors (shown schematically as elements 16) could be used to collect as many as possible on the detectors 14.
  • Standard techniques such as the use of a holographic notch and red pass filter could be used to suppress stray light [2].
  • the input radiation 12 for fluorescence can be polarised to assist with suppression of stray light.
  • the colour centres could be excited with linearly polarised light and some of the detected fluorescence would then be orthogonally polarised with respect to the excitation, enabling efficient filtering with a polariser.
  • this polarisation-sensitive detection it is desirable for the colour centres to be aligned with each other. Lower excitation power has been found experimentally and theoretically to provide higher contrast and hence greater sensitivity to the photons to be detected (see pages 17-24 of PhD thesis reference [13]).
  • Aligning the colour centres with each other also ensures that they behave in the same manner with respect to the radiation to be detected. This will tend to increase measurement sensitivity.
  • the plurality of colour centres may comprise colour centres having different orientations.
  • the different orientations would be sensitive to different excitations (i.e.
  • the variation in performance arises due to the different orientations of the colour centres relative to any external magnetic field.
  • the size of the energy splitting between different spin states depends on the orientation of the external magnetic field relative to the orientation of the colour centre.
  • the detector is configured to operate at room temperature, which is convenient for many applications. However, reducing the temperature of the colour centres will tend to increase the sensitivity of the optically-detected magnetic resonance (ODMR) process [5], so would provide an even more sensitive detector. Some applications demand temperatures above room temperature, which would also be compatible with embodiments of the invention.
  • ODMR optically-detected magnetic resonance
  • the colour centre is a nitrogen vacancy (NV " ) colour centre in diamond.
  • NV " colour centres in diamond exhibit electron-spin-dependent fluorescence allowing the measurement of ODMR [1].
  • EPR electron paramagnetic resonance
  • a magnetic field the required frequency is around 28 GHz per Tesla of applied magnetic field ⁇ 2.9 GHz.
  • Other ways to tune this frequency include the application of strain and electric fields. It is possible to tune the frequency to which the detector is sensitive to anywhere from 1 Hz to 10 THz, both for NV " colour centres in diamond, and other colour centres.
  • any other centre in a solid particularly those which have an ODMR signal.
  • NV " centres are referred to in this document, one or more of these alternatives could be used instead. Furthermore, the use of multiple coupled centres may be more sensitive, so these could also be used instead of NV " centres. Anywhere that diamond is referred to, one or more of these hosts (such as quartz) could be used instead. More than one of these centres could be combined in the same or different host materials to increase the sensitivity and/or permit detection of more than one frequency.
  • Noise photons which exist at the fluorescence frequency may limit the sensitivity of the detector. If there are many centres fluorescing and only one of these absorbs a photon to be detected, then the fluorescence of the other centres may prevent detection. For this reason, it could be advantageous to use a single centre. However, this approach leads to a greatly reduced dynamic range (the output signal is only one bit). Additionally, it can be challenging to direct the photons one wants to detect onto the tiny (atomic scale) colour centre.
  • Figure 2 is a schematic illustration of a detector which addresses the above issues by providing a substrate 4 having a plurality of colour centres and a coupling device that is configured to direct input radiation directly to all of the plurality of colour centres.
  • the provision of a plurality of colour centres increases the dynamic range, and a coupling device 6 directs incoming radiation specifically to the plurality of colour centres.
  • the coupling device 6 comprises an antenna 6C, a coaxial cable 6B and a branched system of wires 6A embedded on or within the substrate 4.
  • the input radiation will be captured by the antenna 6C, conveyed to the branched system of wires 6A by the coaxial cable 6B and directed to individual colour centres located at the tips of the branches of the branched system of wires 6A.
  • the tip region 20 of one of the branches is shown in a magnified inset 20.
  • a single colour centre 22 is provided in the region of the tip with dedicated optics 24 for probing the spin-dependent fluorescence of the colour centre.
  • the optics 24 may comprise optical excitation and detection devices and/or lenses to direct the exciting and/or emitted radiation to their respective targets.
  • the optical excitation and detection could consist of one or more excitation sources (such as a green laser) which could be split up, for example, to excite all of the different single colour centres (or separate sources could be used for each of the colour centres or subsets of the colour centres).
  • the optical detection comprises one or more detectors for the emitted radiation (such as avalanche photo-diodes) to which the signals from all of the different single colour centres could be routed.
  • the coupling device 6 comprises a metal wire split into a system of branches 6A within the substrate 4. This could be achieved using standard lithography techniques, for example, such as optical or electron-beam lithography.
  • the wires may be formed so as to be about 10 microns wide and 100 nm thick, for example.
  • different structures e.g. waveguides may be formed within the substrate 4 for directing the input radiation onto the colour centres.
  • a resonator 25 is provided, for example as a replacement of a portion of the wire in each of one or more of the tip regions of the branched structure shown in Figure 2.
  • the resonator 25 may be of the type illustrated in Figure 3 for example, comprising two parallel, conducting lines 26 and 28 connected to a conducting loop 27.
  • This design is a variant of the commonly used loop-gap resonator [6].
  • the radius of the loop, r can be chosen to be relatively small (e.g. 10 microns) so as to concentrate the magnetic field associated with the input radiation as much as possible onto the atomic-scale colour centre.
  • Using such small sized loops tends to increase the resonant frequency of the resonator above the resonant frequency of the colour centre (for example, in the region of about 3GHz for NV " colour centres in diamond in low magnetic fields), but the frequency can be brought back down to any desired value by adding extra capacitance.
  • This can be achieved by increasing the length L of the resonator, for example, or in other ways, such as by putting in a capacitor of chosen value connecting the two wires 26 and 28.
  • the resonator 25 could be made with 1, 2 or a multitude of stacked planar structures.
  • the two parallel lines 26 and 28 in Figure 3 could be in the same plane as the loop 27, or stacked on top of each other with a dielectric material in between.
  • the resonators 25 can be above and/or below the colour centre.
  • the resonators for different colour centres could be the same, to increase the coupling strength, or different so as to have different resonant frequencies (thereby increasing the bandwidth of operation of the detector
  • the typically required dimensions of the resonator 25 allow convenient fabrication using optical lithography. These length scales are also convenient having regard to the diffraction limit of visible light for ODMR readout (it is hard to focus light down to much less than its wavelength), as well as for the skin depths of the radiation to be detected (e.g. microwaves) in metal (the metal should generally be thicker than the skin depth to avoid too much of the input radiation power passing right through the metal). However, in principle any length scale is appropriate.
  • the detector is configured for use in an apparatus for performing electron paramagnetic resonance (EPR) imaging.
  • EPR electron paramagnetic resonance
  • the detector is configured to detect the radiation absorbed or emitted due to EPR in the object being imaged.
  • EPR is also known as electron spin resonance (ESR) and electron magnetic resonance (EMR).
  • ESR electron spin resonance
  • EMR electron magnetic resonance
  • Most electron spins have a g-factor of around 2, meaning that the frequency needed to drive EPR is around 28 GHz per Tesla of magnetic field applied.
  • EMR electron spin resonance
  • EMR electron magnetic resonance
  • Most electron spins have a g-factor of around 2, meaning that the frequency needed to drive EPR is around 28 GHz per Tesla of magnetic field applied.
  • the detector 2 it is required that the magnetic field experienced by the colour centres should be adjusted to meet the ODMR resonance condition. When the sample is in a large magnetic field of 1 T or more, this could be achieved simply by placing the colour centres slightly outside of the field-centre of the magnet used for the
  • the detection it is possible for the detection to be performed in transmission (where the microwaves pass through the sample to the detector) or in reflection (where the microwaves are reflected from the sample to the detector with or without the aid of a circulator to reduce the microwaves coming directly to the detector from their source).
  • Embodiments of the detector could be used with both configurations.
  • the free-induction decay (FID) as the signal by sending in one radiation (e.g. microwave) pulse to the sample and measuring the radiation emitted by the sample.
  • one radiation e.g. microwave
  • the colour centres it is desirable for the colour centres to refresh fast, on a timescale of ns. As NV " centres do not refresh as fast as this, one may prefer other centres such as the silicon- vacancy centres [15, 16] or the vacancy-related defects [14].
  • NMR experiments are performed more frequently than EPR because unpaired nuclear spins are more common than unpaired electron spins.
  • Magnetic resonance imaging (MRI) is a popular example of NMR.
  • Embodiments of the detector can be used for detecting NMR in a similar way to the EPR case described above.
  • the resonant frequency for NMR tends to be around 1000 times lower than for EPR.
  • the magnetic field applied to the sample in an NMR experiment is generally kept constant, in contrast to many EPR experiments.
  • a mobile phone and/or base station comprises a detector according to an embodiment of the invention that is tuned to detect input radiation of less than 700 MHz, preferably less than 500 MHz.
  • the detector is configured to detect radiation having a frequency corresponding to the EPR frequencies of the colour centres involved. As discussed, these frequencies are dependent on the applied magnetic field. This allows the frequency sensitivity to be tuned so as to be appropriate to particular applications. However, the sensitivity to magnetic field can also be exploited directly by using the colour centres as sensitive magnetometers.
  • this effect is exploited to provide a detector (acting as a magnetometer) for use in single-molecule NMR following references [23] and [24].
  • a colour centre is used directly to detect a change in magnetic field at the colour centre caused by the magnetism (spin) of one or more nuclei that are brought into close proximity with the colour centres.
  • the change in magnetic field is detected by monitoring a change in the EPR characteristics of the colour centre (e.g. by monitoring the variation in fluorescence as a function of the frequency of applied microwave radiation.
  • the sample in order to speed up sampling of the different NMR resonances, is subjected to a high magnetic field (e.g. > 5T, preferably >10T, 15T, 20T or 25T).
  • a high magnetic field e.g. > 5T, preferably >10T, 15T, 20T or 25T.
  • a sample 32 to be tested is mounted on a probe and inserted into the bore of a high field magnet.
  • the sample 32 is mounted or received in a sample receiver 30 that is configured to allow use of colour centres as magnetometers.
  • the sample 32 may for example be adsorbed, as a dry solid, or may be in solution (but not rotating too quickly compared to the experimental timescale). An example of such a configuration is shown in Figure 4.
  • the sample receiver 30 comprises a substrate 34 comprising a plurality of colour centres 22 (see lower magnified inset 35, which is a magnified view of a portion of the sample receiver 30 at the interface between the sample 32 and the receiver 30).
  • Each of the colour centres 22 is provided in close proximity to a different portion of the sample 32.
  • the colour centres 22 will be influenced by molecules that have various different orientations relative to the colour centres, which allows the colour centres collectively to sample different nuclei and/or combinations of nuclei of the molecule under study at the same time.
  • a coupling system 38 may be provided for directing electromagnetic radiation to the colour centres 22 and to the sample 32 in order respectively to control the electron spins of the colour centres using electron paramagnetic resonance and the nuclear spins of the sample using nuclear magnetic resonance.
  • the coupling system 38 may be referred to as a combination of a "first coupling system” (for directing electromagnetic radiation to control the spins of the colour centres) and a “second coupling system” (for directing electromagnetic radiation to control the nuclear spins), which may be integrated into a single coupling system (as shown) or may be separate coupling systems.
  • a plurality of optical fibres 36 are provided in the sample receiver 30 for the purposes of individually probing the fluorescence of each of the different colour centres 22.
  • the optical fibres 36 may be considered as part of a third coupling system.
  • the upper magnified inset 37 depicts a magnified top view of a portion of the substrate receiver 30 and shows how the colour centres 22 can be provided in a two- dimensional array with dedicated loop-gap resonators 40 associated with each of the different colour centres 22. It is understood that each of the colour centres 22 in the two-dimensional array shown in the inset 37 will have its own optical fibre 36 positioned beneath for probing the spin state of the colour centre 22 using fluorescence.
  • the approach of this embodiment allows single-molecule NMR experiments to be performed sensitively and efficiently (quickly).
  • the desirable static magnetic field for NMR is as high as possible to get more spectral resolution, but is currently limited to between 20 and 30 T by the cost of making high-field superconducting magnets.
  • the frequency needed to excite the electron spins becomes high: 140 to 850 GHz.
  • This frequency region is technologically inconvenient, but accessible with modern equipment. It is very convenient for making small loop-gap resonators with r ⁇ 50 um scale, as no extra capacitance is needed, allowing L ⁇ 0.
  • the optical fibres 36 have a diameter of 100 um. Allowing one per colour centre, this would leave room for over 1000 single-molecule colour centre NMR spectrometers to be squeezed into a standard 4 mm diameter chip. Such a chip would fit into existing NMR spectrometers, simply by replacing the NMR probe (the magnets and consoles cost more than the probes). All of the colour centre spectrometers in the array would experience the same static magnetic field and RF field (a lower frequency for exciting the nuclear spins) because their homogeneity across several mm is standard practice in commercial NMR.
  • the superconducting magnet would not need to be as homogeneous as existing NMR magnets as the sample in each experiment would be on the molecular scale over which the magnetic field would look very homogeneous in comparison with the mm-scale samples currently used.
  • a sample would cover the 4 mm scale chip and NMR information about 1000 molecular orientations would come out simultaneously.
  • Each of the colour centre spectrometers would see only the part of the molecule closest to it: the colour centre would only see 1-5 nuclei that are the closest to it, but these are coupled to others in the molecule which could be probed by sending in NMR pulses to find the resonances. Analysing this information with dedicated software would allow the puzzle pieces to be put together revealing the full shape of the molecule.
  • the detectors may be tuned to be sensitive to frequencies in the broad range of lHz to lOTHz (although in other embodiments the invention may find use outside this range). However, in practice, the majority of applications will fall in the range lMHz to 2 THz and, within this, the most preferred frequency range is 100MHz to 10GHz.
  • Greentree & S. Prawer Chromium single-photon emitters in diamond fabricated by ion implantation, Physical Review B 81, 121201(R) (2010). [18] I. Aharonovich, S. Castelletto, D. A. Simpson, A. D. Greentree & S. Prawer, Photophysics of chromium-related diamond single-photon emitters, Physical Review A 81, 043813 (2010).

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Abstract

La présente invention porte sur des détecteurs et des procédés de détection de rayonnement électromagnétique et/ou de résonance paramagnétique électronique (EPR)/résonance magnétique nucléaire (RMN), qui exploitent la fluorescence dépendante du spin électronique d'un centre coloré dans un solide. Selon un exemple, un détecteur comprend un substrat agencé pour recevoir un rayonnement d'entrée à détecter et comprenant un centre coloré d'un type qui présente une fluorescence dépendante du spin électronique, et une section de mesure de spin destinée à sonder l'état de spin du centre coloré à l'aide de fluorescence, détectant ainsi un rayonnement d'entrée qui est de manière à changer l'état de spin du centre coloré.
PCT/GB2014/052289 2013-07-30 2014-07-25 Détecteur sensible WO2015015172A1 (fr)

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