Bias magnet array for magnetometer

Information

  • Patent Grant
  • 10379174
  • Patent Number
    10,379,174
  • Date Filed
    Friday, March 24, 2017
    7 years ago
  • Date Issued
    Tuesday, August 13, 2019
    5 years ago
Abstract
A magnetometer includes a light source that provides excitation light and a magneto-optical defect center material with at least one defect center that transmits emitted light when excited by the excitation light. The magnetometer also includes a light sensor that receives the emitted light and a plurality of magnets that provide a bias magnetic field to the magneto-optical defect center material. The magnetometer further includes a ring magnet holder that has an outer ring with an outside surface and a plurality of holders extending from the ring. The plurality of holders hold the plurality of magnets in a same orientation with respect to one another. The magnetometer further includes a mount that has an inside surface. The outside surface of the outer ring slides along the inside surface of the mount.
Description
TECHNICAL FIELD

The present disclosure relates, in general, to magnetometers using magneto-optical defect center materials. More particularly, the present disclosure relates to bias magnets within such a magnetometer.


BACKGROUND

The following description is provided to assist the understanding of the reader. None of the information provided or references cited is admitted to be prior art. Some magnetometers use magneto-optical defect center materials to determine a magnetic field. Such magnetometers can apply a magnetic bias to the magneto-optical defect center materials. There is a desire for improving and optimizing a method for applying the magnetic bias to the magneto-optical defect center materials while maintaining functionality of the magnetometer and/or adjustability of the magnetometer.


SUMMARY

Embodiments of a magnetometer may include a light source configured to provide excitation light and a magneto-optical defect center material with at least one defect center that transmits emitted light when excited by the excitation light. The magnetometers may also include a light sensor configured to receive the emitted light and a plurality of magnets that may be configured to provide a bias magnetic field to the magneto-optical defect center material. The magnetometer may further include a ring magnet holder that has an outer ring with an outside surface and a plurality of holders extending from the ring. The plurality of holders may be configured to hold the plurality of magnets in a same orientation with respect to one another. The magnetometer may further include a mount that has an inside surface. The outside surface of the outer ring may slide along the inside surface of the mount.


Some device embodiments may include a plurality of magnets that can be configured to provide a bias magnetic field to a magneto-optical defect center material. The devices may also include a ring magnet holder that has an outer ring with an outside surface and a plurality of holders extending from the ring. The plurality of holders may be configured to hold a plurality of magnets in a same orientation with respect to one another. The devices may further include a mount that has an inside surface. The outside surface of the outer ring may slide along the inside surface of the mount.


The foregoing summary is illustrative only and is not intended to be in any way limiting. In addition to the illustrative aspects, embodiments, and features described above, further aspects, embodiments, and features will become apparent by reference to the following drawings and the detailed description.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 illustrates one orientation of an NV center in a magneto-optical defect center material lattice in accordance with some illustrative embodiments.



FIG. 2 is an energy level diagram showing energy levels of spin states for an NV center in accordance with some illustrative embodiments.



FIG. 3 is a schematic diagram illustrating a NV center magnetic sensor system in accordance with some illustrative embodiments.



FIG. 4 is a graph illustrating fluorescence as a function of an applied RF frequency of an NV center along a given direction for a zero magnetic field in accordance with some illustrative embodiments.



FIG. 5 is a graph illustrating fluorescence as a function of an applied RF frequency for four different NV center orientations for a non-zero magnetic field in accordance with some illustrative embodiments.



FIG. 6 is a schematic diagram illustrating a magnetic field detection system in accordance with some illustrative embodiments.



FIG. 7 is an illustration of an inside view of a magnetometer in accordance with some illustrative embodiments.



FIG. 8 is an illustration of a magnet mount assembly in accordance with some illustrative embodiments.



FIGS. 9 and 10 are illustrations of parts of a disassembled magnet ring mount in accordance with some illustrative embodiments.



FIG. 11 is an illustration of a magnet ring mount showing locations of magnets in accordance with some illustrative embodiments.



FIGS. 12 and 13 are illustrations of a bias magnet ring mount in accordance with some illustrative embodiments.





The foregoing and other features will become apparent from the following description and appended claims, taken in conjunction with the accompanying drawings. Understanding that these drawings depict only several embodiments in accordance with the disclosure and are, therefore, not to be considered limiting of its scope, the disclosure will be described with additional specificity and detail through use of the accompanying drawings.


DETAILED DESCRIPTION

In the following detailed description, reference is made to the accompanying drawings, which form a part hereof. In the drawings, similar symbols typically identify similar components, unless context dictates otherwise. The illustrative embodiments described in the detailed description, drawings, and claims are not meant to be limiting. Other embodiments may be utilized, and other changes may be made, without departing from the spirit or scope of the subject matter presented here. It will be readily understood that the aspects of the present disclosure, as generally described herein, and illustrated in the figures, can be arranged, substituted, combined, and designed in a wide variety of different configurations, all of which are explicitly contemplated and make part of this disclosure.


Magnetometers can use a magneto optical defect center material to determine a magnitude and direction of an external magnetic field. For example, the magneto optical defect center material can be a diamond with nitrogen vacancy (NV) centers. In other examples, any other suitable material with defect centers may be used. A bias magnetic field can be applied to the magneto optical defect center material. As explained in greater detail below, the bias magnetic field can be applied to distinguish an effect of a magnetic field on different axes of the defect center.


It can be advantageous in some embodiments to be able to adjust the bias magnetic field to achieve a desired output from the magneto optical defect center material, as discussed in greater detail below. In some illustrative embodiments, a magnet ring mount can hold a bias magnet ring in place around the magneto optical defect center material. The bias magnet ring can hold a plurality of magnets in place, and the magnets can apply the bias magnetic field to the magneto optical defect center material. The bias magnetic ring may be unsecured (e.g., via set screws) from the magnet ring mount and moved around the magneto optical defect center material to adjust the direction of the bias magnetic field that is applied to the magneto optical defect center material.


The NV center in a diamond comprises a substitutional nitrogen atom in a lattice site adjacent a carbon vacancy as shown in FIG. 1. The NV center may have four orientations, each corresponding to a different crystallographic orientation of the diamond lattice. Although FIG. 1 shows the NV center in a diamond, the same or similar principals can be applied to defect centers in any suitable magneto-optical defect center material.


The NV center may exist in a neutral charge state or a negative charge state. Conventionally, the neutral charge state uses the nomenclature NV0, while the negative charge state uses the nomenclature NV, which is adopted in this description.


The NV center has a number of electrons, including three unpaired electrons, each one from the vacancy to a respective of the three carbon atoms adjacent to the vacancy, and a pair of electrons between the nitrogen and the vacancy. The NV center, which is in the negatively charged state, also includes an extra electron.


The NV center has rotational symmetry, and as shown in FIG. 2, has a ground state, which is a spin triplet with 3A2 symmetry with one spin state ms=0, and two further spin states ms=+1, and ms=−1. In the absence of an external magnetic field, the ms=+1 energy levels are offset from the ms=0 due to spin-spin interactions, and the ms=±1 energy levels are degenerate, i.e., they have the same energy. The ms=0 spin state energy level is split from the ms=±1 energy levels by an energy of 2.87 GHz for a zero external magnetic field.


Introducing an external magnetic field with a component along the NV axis lifts the degeneracy of the ms=±1 energy levels, splitting the energy levels ms=±1 by an amount 2 gμBBz, where g is the g-factor, μB is the Bohr magneton, and Bz is the component of the external magnetic field along the NV axis. This relationship is correct to a first order and inclusion of higher order corrections is a straightforward matter and will not affect the computational and logic steps in the systems and methods described below.


The NV center electronic structure further includes an excited triplet state 3E with corresponding ms=0 and ms=±1 spin states. The optical transitions between the ground state 3A2 and the excited triplet 3E are predominantly spin conserving, meaning that the optical transitions are between initial and final states that have the same spin. For a direct transition between the excited triplet 3E and the ground state 3A2, a photon of red light is emitted with a photon energy corresponding to the energy difference between the energy levels of the transitions.


There is, however, an alternative non-radiative decay route from the triplet 3E to the ground state 3A2 via intermediate electron states, which are thought to be intermediate singlet states A, E with intermediate energy levels. Significantly, the transition rate from the ms=±1 spin states of the excited triplet 3E to the intermediate energy levels is significantly greater than the transition rate from the ms=0 spin state of the excited triplet 3E to the intermediate energy levels. The transition from the singlet states A, E to the ground state triplet 3A2 predominantly decays to the ms=0 spin state over the ms=±1 spins states. These features of the decay from the excited triplet 3E state via the intermediate singlet states A, E to the ground state triplet 3A2 allows that if optical excitation is provided to the system, the optical excitation will eventually pump the NV center into the ms=0 spin state of the ground state 3A2. In this way, the population of the ms=0 spin state of the ground state 3A2 may be “reset” to a maximum polarization determined by the decay rates from the triplet 3E to the intermediate singlet states.


Another feature of the decay is that the fluorescence intensity due to optically stimulating the excited triplet 3E state is less for the ms=±1 states than for the ms=0 spin state. This is so because the decay via the intermediate states does not result in a photon emitted in the fluorescence band, and because of the greater probability that the ms=±1 states of the excited triplet 3E state will decay via the non-radiative decay path. The lower fluorescence intensity for the ms=±1 states than for the ms=0 spin state allows the fluorescence intensity to be used to determine the spin state. As the population of the ms=±1 states increases relative to the ms=0 spin, the overall fluorescence intensity will be reduced.



FIG. 3 is a schematic diagram illustrating a conventional magneto-optical defect center material magnetic sensor system 300 that uses fluorescence intensity to distinguish the ms=±1 states, and to measure the magnetic field based on the energy difference between the ms=+1 state and the ms=−1 state. The system 300 includes an optical excitation source 310, which directs optical excitation to a magneto-optical defect center material 320 with defect centers. The system further includes an RF excitation source 330, which provides RF radiation to the magneto-optical defect center material 320. Light from the magneto-optical defect center material may go through an optical filter 350 and to an optical detector 340.


The RF excitation source 330 may be a microwave coil, for example. The RF excitation source 330, when emitting RF radiation with a photon energy resonant with the transition energy between ground ms=0 spin state and the ms=+1 spin state, excites a transition between those spin states. For such a resonance, the spin state cycles between ground ms=0 spin state and the ms=+1 spin state, reducing the population in the ms=0 spin state and reducing the overall fluorescence at resonances. Similarly, resonance occurs between the ms=0 spin state and the ms=−1 spin state of the ground state when the photon energy of the RF radiation emitted by the RF excitation source is the difference in energies of the ms=0 spin state and the ms=−1 spin state, or between the ms=0 spin state and the ms=+1 spin state, there is a decrease in the fluorescence intensity.


The optical excitation source 310 may be a laser or a light emitting diode, for example, which emits light in the green, for example. The optical excitation source 310 induces fluorescence in the red, which corresponds to an electronic transition from the excited state to the ground state. Light from the magneto-optical defect center material 320 is directed through the optical filter 350 to filter out light in the excitation band (in the green, for example), and to pass light in the red fluorescence band, which in turn is detected by the detector 340. The optical excitation light source 310, in addition to exciting fluorescence in the diamond material 320, also serves to reset the population of the ms=0 spin state of the ground state 3A2 to a maximum polarization, or other desired polarization.


For continuous wave excitation, the optical excitation source 310 continuously pumps the defect centers, and the RF excitation source 330 transmits a radio frequency field that sweeps across a frequency range that includes the zero splitting (when the ms=±1 spin states have the same energy) photon energy of 2.87 GHz. The light from optical excitation source 310 passes in front of RF excitation source 330. The fluorescence for an RF sweep corresponding to a magneto-optical defect center material 320 with defect centers aligned along a single direction is shown in FIG. 4 for different magnetic field components Bz along the defect axis, where the energy splitting between the ms=−1 spin state and the ms=+1 spin state increases with Bz. Thus, the component Bz may be determined. Optical excitation schemes other than continuous wave excitation are contemplated, such as excitation schemes involving pulsed optical excitation, and pulsed RF excitation. Examples of pulsed excitation schemes include Ramsey pulse, and spin echo pulse sequence.


In general, the magneto-optical defect center material 320 may have defect centers aligned along directions of four different orientation classes. FIG. 5 illustrates fluorescence as a function of RF frequency for the case where the magneto-optical defect center material 320 has defect centers aligned along directions of four different orientation classes. In this case, the component Bz along each of the different orientations may be determined. These results, along with the known orientation of crystallographic planes of a magneto-optical defect center material lattice, allow not only the magnitude of the external magnetic field to be determined, but also the direction of the magnetic field.



FIG. 3 illustrates a defect center magnetic sensor system 300 with magneto-optical defect center material 320 with a plurality of defect centers, in general. The magnetic sensor system 300 may employ any suitable magneto-optical defect center material with a plurality of magneto-optical defect centers. The electronic spin state energies of the magneto-optical defect centers shift with magnetic field, and the optical response, such as fluorescence, for the different spin states is not the same for all of the different spin states. In this way, the magnetic field may be determined based on optical excitation, and possibly RF excitation.



FIG. 6 is a schematic diagram of a system 600 for a magnetic field detection system according to some embodiments. The system 600 includes an optical excitation source 610, which directs optical excitation to a magneto-optical defect center material 620 with defect centers. An RF excitation source 630 provides RF radiation to the magneto-optical defect center material 620. A magnetic field generator 670 generates a magnetic field, which is detected at the magneto-optical defect center material 620.


The magnetic field generator 670 may generate magnetic fields with orthogonal polarizations, for example. In this regard, the magnetic field generator 670 may include two or more magnetic field generators, such as two or more Helmholtz coils. The two or more magnetic field generators may be configured to provide a magnetic field having a predetermined direction, each of which provide a relatively uniform magnetic field at the magneto-optical defect center material 620. The predetermined directions may be orthogonal to one another. In addition, the two or more magnetic field generators of the magnetic field generator 670 may be disposed at the same position, or may be separated from each other. In the case that the two or more magnetic field generators are separated from each other, the two or more magnetic field generators may be arranged in an array, such as a one-dimensional or two-dimensional array, for example.


The system 600 may be arranged to include one or more optical detection systems 605, where each of the optical detection systems 605 includes the optical detector 640, optical excitation source 610, and Magneto-optical defect center material 620. Furthermore, the magnetic field generator 670 may have a relatively high power as compared to the optical detection systems 605. In this way, the optical systems 605 may be deployed in an environment that requires a relatively lower power for the optical systems 605, while the magnetic field generator 670 may be deployed in an environment that has a relatively high power available for the magnetic field generator 670 so as to apply a relatively strong magnetic field.


The system 600 further includes a controller 680 arranged to receive a light detection signal from the optical detector 640 and to control the optical excitation source 610, the RF excitation source 630, and a second magnetic field generator (not shown in FIG. 6). The controller may be a single controller, or multiple controllers. For a controller including multiple controllers, each of the controllers may perform different functions, such as controlling different components of the system 600. The second magnetic field generator may be controlled by the controller 680 via an amplifier 660, for example.


The RF excitation source 630 may be a microwave coil, for example behind the light of the optical excitation source 610. The RF excitation source 630 is controlled to emit RF radiation with a photon energy resonant with the transition energy between the ground ms=0 spin state and the ms=±1 spin states as discussed above with respect to FIG. 3.


The optical excitation source 610 may be a laser or a light emitting diode, for example, which emits light in the green, for example. The optical excitation source 610 induces fluorescence in the red from the Magneto-optical defect center material 620, where the fluorescence corresponds to an electronic transition from the excited state to the ground state. Light from the Magneto-optical defect center material 620 is directed through the optical filter 650 to filter out light in the excitation band (in the green, for example), and to pass light in the red fluorescence band, which in turn is detected by the optical detector 640. The optical excitation light source 610, in addition to exciting fluorescence in the Magneto-optical defect center material 620, also serves to reset the population of the ms=0 spin state of the ground state 3A2 to a maximum polarization, or other desired polarization.


The controller 680 is arranged to receive a light detection signal from the optical detector 640 and to control the optical excitation source 610, the RF excitation source 630, and the second magnetic field generator (not shown in FIG. 6). The controller may include a processor 682 and a memory 684, in order to control the operation of the optical excitation source 610, the RF excitation source 630, and the second magnetic field generator. The memory 684, which may include a nontransitory computer readable medium, may store instructions to allow the operation of the optical excitation source 610, the RF excitation source 630, and the second magnetic field generator to be controlled. That is, the controller 680 may be programmed to provide control.



FIG. 7 is an illustration of an inside view of a magnetometer in accordance with some illustrative embodiments. An illustrative magnetometer 700 includes a housing 705, light sources 710 and 715, a magneto-optical defect center material 720, a light detector 725, a magnet ring mount 730, and a bias magnet ring 735. In alternative embodiments, additional, fewer, and/or different elements may be used. For example, although two light sources 710 and 715 are shown in the embodiment of FIG. 7, any suitable number of light sources can be used, such as one, three, four, etc. light sources.


As noted above, a bias magnetic field may be applied to the magneto-optical defect center material 720. In the embodiment illustrated in FIG. 7, permanent magnets are mounted to the bias magnet ring 735, which is secured within the magnet ring mount 730. The magnet ring mount 730 is mounted or fixed within the housing 705 such that the magnet ring mount 730 does not move within the housing 705. Similarly, the light sources 710 and 715 are mounted within the housing 705 such that the light sources 710 and 715 do not move within the housing 705.


As shown in FIG. 7, the magneto-optical defect center material 720 is mounted within the magnetic ring mount 730, but the light sources 710 and 715 are mounted outside of the magnetic ring mount 730. The light sources 710 and 715 transmit light to the magneto-optical defect center material 720 which excites the defect centers, and light emitted from the defect centers is detected by the light detector 725. In the embodiments shown in FIG. 7, the light sources 710 and 715 transmit the light such that the magnet ring mount 730 and the bias magnet ring 735 do not interfere with the transmission of the light from the light sources 710 and 715 to the magneto-optical defect material 720.



FIG. 8 is an illustration of a magnet mount assembly in accordance with some illustrative embodiments. An illustrative magnet mount assembly 800 includes the magnet ring mount 730 and the bias magnet ring 735. In alternative embodiments, additional, fewer, and/or different elements may be used.


As shown in FIG. 8, the magnet ring mount 730 includes a first portion 805 and a second portion 810 held together with fasteners 820. The bias magnet ring 735 can be fixed within the magnet ring mount 730. The bias magnet ring 735 can hold magnets such that a uniform or substantially uniform magnetic field is applied to a central portion of the magnet mount assembly 800. For example, the uniform magnetic field can be applied to the magneto-optical defect center material 720.


The magnet mount assembly 800 includes through-holes 815. The through-holes 815 can be sufficiently large to allow light from the light sources 710 and 715 to pass into a center portion of the magnet mount assembly 800 (e.g., to apply light to the magneto-optical defect center material 720). As noted above, the magnetometer 700 may include any suitable number of light sources 710 and 715. Similarly, the magnet mount assembly 800 may include any suitable number of through-holes 815. In some illustrative embodiments, the magnet mount assembly 800 incudes the same number of through-holes 815 as the magnetometer 700 includes light sources 710 and 715. In alternative embodiments, the magnet mount assembly 800 includes a different number of through-holes 815 as the magnetometer 700 includes light sources 710 and 715. For example, two or more light sources 710 and 715 may pass light through the same through-hole 815. In another example, one or more through-holes 815 may not have light passing therethrough.


The magnet mount assembly 800 as shown in FIG. 8 includes six fasteners 820. The fasteners 820 can be used to secure the first portion 805 to the second portion 810. In some illustrative embodiments, the fasteners 820 can be used to secure the magnet mount assembly 800 to the housing 705 of the magnetometer 700. The fasteners 820 can be any suitable device for securing the first portion 805 to the second portion 810. In the embodiment shown in FIG. 8, the fasteners 820 are screws. Other examples of fasteners 820 may include bolts, studs, nuts, clips, etc. In alternative embodiments, any suitable means of securing the first portion 805 and the second portion 810 to one another, such as glue, welds, epoxy, etc. Although FIG. 8 shows six fasteners 820 being used, any other suitable number can be used. For example, the magnet mount assembly 800 may have one, two, three, five, ten, etc. fasteners 820.


As shown in FIG. 8, the inside surface of the magnet ring mount 730 is circular or semi-spherical and the outside surface is an octagonal prism. In such an embodiment, a center of the circular shape or semi-spherical shape of the inside surface is on a central axis of the octagonal prism of the outside surface. Any other suitable shapes may be used. For example, the inside surface of the magnet ring mount 730 may be elliptical. In another example, the outside surface of the magnet ring mount 730 may have more or fewer sides than eight.


In some illustrative embodiments, the inner diameter (e.g., the inner spherical diameter) of the magnet ring mount 730 is 2.75 inches. In such an embodiment, the tolerance may be +0.002 inches and −0.000 inches. In alternative embodiments, the inner diameter of the magnet ring mount 730 is greater than or less than 2.75 inches, and any suitable tolerance may be used.


As shown in FIG. 8, the bias magnet ring 735 can include an outside ring that is circular. In some illustrative embodiments, the outside circumference of the bias magnet ring 735 is the same or slightly less than the inside diameter of the magnet ring mount 730. In such an embodiment, when not secured, the bias magnet ring 735 can move freely within the magnet ring mount 730. As discussed in greater detail below, the bias magnet ring 735 can be secured in place inside of the magnet ring mount 730 using, for example, set screws.


The magnet ring mount 730 and the bias magnet ring 735 may be made of any suitable material. In some illustrative embodiments, the magnet ring mount 730 and the bias magnet ring 735 are non-ferrous and/or non-magnetic. For example, the magnet ring mount 730 and the bias magnet ring 735 may be made of plastic (e.g., Black Noryl® PPO™, polystyrene, polyphenylene ether, etc.), titanium (e.g., Grade 5, Ti 6Al-4V, etc.), aluminum (e.g., 6061-T6 per ASTM B209, may have a chemical conversion coating per military standard MIL-DTL-5541, etc.), etc. The fasteners 820, the set screws, and any other component of the system may be made of the same or similar materials.



FIGS. 9 and 10 are illustrations of parts of a disassembled magnet ring mount in accordance with some illustrative embodiments. FIG. 9 is an illustration of the first portion 805 of the magnet ring mount 730, and FIG. 10 is an illustration of the second portion 810 of the magnet ring mount 730. The first portion 805 includes fastener holes 905, and the second portion 810 includes fastener holes 1005. In some illustrative embodiments, the fastener holes 905 align with corresponding fastener holes 1005 to accept the fasteners 820. The first portion 805 includes a hole larger than the fastener holes 905 above the fastener holes 905 to accept a head of the fasteners 820 (e.g., the head of a screw). For example, the fastener holes 905 and the fastener holes 1005 may be 0.1 inches in diameter and may be suitable to accept fasteners 820 that are #2-56 screws. In some illustrative embodiments, the fasteners 820 screw into threaded holes in the housing 705 or a surface secured to the housing 705 (e.g., a circuit board). In alternative embodiments, any other suitable securing mechanism or arrangement may be used.


The first portion 805 of the magnet ring mount 730 includes a height 950, a length 951, and a width 952. In some illustrative embodiments, the width 952 can be as wide as the length 951 is long. In some illustrative embodiments, the height 950 is 0.475 inches, and the width 952 and the length 951 are 2.875 inches each. In alternative embodiments, any other suitable dimensions may be used.


The second portion 810 of the magnet ring mount 730 includes a height 1050, a length 1051, and a width 1052. In some illustrative embodiments, the width 1052 can be as wide as the length 1051 is long. In the embodiments shown in FIGS. 9 and 10, the height 950 is the same as the height 1050, the length 951 is the same as the length 1051, and the width 952 is the same as the width 1052. In some such embodiments, the height 1050 is 0.475 inches, and the width 1052 and the length 1051 are 2.875 inches each. In such an embodiment, the inside surface 910 and the inside surface 1010 are matching but opposite portions of a sphere. That is, the circle at which the inside surface 910 and the inside surface 1010 meet is a circumference of a sphere, and the inside surface 910 and the inside surface 1010 are along the sphere. In alternative embodiments, any other suitable dimensions may be used.



FIG. 11 is an illustration of a magnet ring mount showing locations of magnets in accordance with some illustrative embodiments. FIG. 11 includes the magnet ring mount 730 and magnets 1105. In FIG. 11, six sets of three magnets 1105 are shown. Each magnet 1105 in a set are arranged in the same direction (e.g., the poles of each magnet 1105 are pointed in the same direction). In alternative embodiments, additional, fewer, and/or different elements may be used. For example, in alternative embodiments, each set of magnets 1105 may include greater than or fewer than three magnets 1105. Similarly, the total number of magnets 1105 may be greater than or fewer than eighteen.



FIG. 11 shows an illustrative arrangement of the magnets 1105 within the magnet ring mount 730 without the bias magnet ring 735. Although the bias magnet ring 735 is not shown, the bias magnet ring 735 may hold the magnets 1105 in the same position relative to one another. But, the bias magnet ring 735 may move within the magnet ring mount 730 while maintaining the magnets 1105 in the same position relative to one another. Accordingly, the magnets 1105 may be rotated around the center portion of the bias magnet ring 735 and/or the magnet ring mount 730 (e.g., around the magneto-optical defect center material 720). For reference, a detailed discussion of diamond axes crystal alignment and magnet orientation is provided in U.S. patent application Ser. No. 15/003,718 (now U.S. Pat. No. 9,541,610) and U.S. patent application Ser. No. 15/003,704, both filed on Jan. 21, 2016, and both of which are incorporated herein by reference in their entireties.



FIGS. 12 and 13 are illustrations of a bias magnet ring mount in accordance with some illustrative embodiments. The bias magnet ring 735 includes magnet holders 1205 with magnet holes 1210 and securing tabs 1215 with set screw holes 1220. In alternative embodiments, additional, fewer, and/or different elements may be used.


As shown in FIGS. 12 and 13, the bias magnet ring 735 has an outer ring, and the magnet holders 1205 and the securing tabs 1215 are fixed to the outer ring. In some illustrative embodiments, the outside diameter 1250 of the outer ring and the bias magnet ring 735 is 2.745 inches. The height 1251 of the magnet holders 1205 can be 0.290 inches. In some illustrative embodiments, the outside surface of the outer ring is spherically shaped to fit within and slide along the inner surface 910 and the inner surface 1010.


As noted above, the magnet holders 1205 have magnet holes 1210. The magnet holes 1210 may hold the magnets 1105 in the orientation to one another shown in FIG. 11. The securing tabs 1215 may each include one or more set screw holes 1220. The set screw holes 1220 may be configured to receive a set screw. For example, the set screw holes 1220 may be threaded. In some illustrative embodiments, set screws may be threaded into the set screw holes 1220 and be pressed against the inner surface 910 and/or the inner surface 1010 to secure the bias magnet ring 735 within the magnet ring mount 730. In some illustrative embodiments, the set screws 1220 may be #2-56 screws. In alternative embodiments, any other suitable set screws may be used.


In the embodiment shown in FIG. 13, two of the securing tabs 1215 each include one set screw hole 1220 and six through-holes 1305. Each of the six through-holes 1305 can be used to drill or otherwise form the magnet holes 1210. For example, each of the through-holes 1305 may be aligned along a same central axis as a corresponding magnet hole 1210. For example, the inside diameter of the magnet holes 1210 can be 0.070 inches. The inside diameter of the through-holes 1305 can be the same or larger than the inside diameter of the magnet holes 1210. Following the example, the inside diameter of the through-holes 1305 may be 0.070 inches (or larger). In alternative embodiments, any other suitable inside diameters may be used.


Thus, the magnet mount assembly 800 can be used to adjust the magnetic bias applied to the magneto-optical defect center material 720 by moving the magnets 1105 about the magneto-optical defect center material 720. Similarly, once a desired position is selected, the bias magnet ring 735 may be secured within the magnet ring mount 730.


As noted above with respect to FIGS. 4 and 5, each of the dips (e.g., Lorentzians) in the graphs may correspond to one or more axes of the defect centers within the magneto-optical defect center material 720. The bias magnetic field applied to the magneto-optical defect center material 720 may adjust the order and orientation of the Lorentzian dips in the graphs. Accordingly, there are forty-eight unique orientations of the Lorentzians such that each Lorentzian is distinguishable from the others (e.g., as in the graph of FIG. 5). Thus, there are forty-eight unique positions of the magnets 1105 around the magneto-optical defect center material 720 corresponding to each of the forty-eight orientations of the Lorentzians.


In some illustrative embodiments, the magnet ring mount 730 is movable within the bias magnet ring 735 and the housing 705 such that twelve of the forty-eight positions of the magnets 1105 are accessible. That is, the magnet ring mount 730 cannot be positioned into all of the forty-eight positions because the magnet ring mount 730 would interfere with the housing 705, which may span across the top and bottom of the magnet ring mount 730. In some instances, only a portion of the twelve positions may position the bias magnet ring 735 within the magnet ring mount 730 such that the bias magnet ring 735 does not interfere with the light that passes through the through-holes 815. In some illustrative embodiments, the bias magnet ring 735 is positioned such that the Lorentzians are distinguishable from one another and such that the light is not interfered with as it passes through the through-hole 815 to the magneto-optical defect center material 720.


In some illustrative embodiments, any of the operations described herein can be implemented at least in part as computer-readable instructions stored on a computer-readable memory. Upon execution of the computer-readable instructions by a processor, the computer-readable instructions can cause a node to perform the operations.


The herein described subject matter sometimes illustrates different components contained within, or connected with, different other components. It is to be understood that such depicted architectures are merely exemplary, and that in fact many other architectures can be implemented which achieve the same functionality. In a conceptual sense, any arrangement of components to achieve the same functionality is effectively “associated” such that the desired functionality is achieved. Hence, any two components herein combined to achieve a particular functionality can be seen as “associated with” each other such that the desired functionality is achieved, irrespective of architectures or intermedial components. Likewise, any two components so associated can also be viewed as being “operably connected,” or “operably coupled,” to each other to achieve the desired functionality, and any two components capable of being so associated can also be viewed as being “operably couplable,” to each other to achieve the desired functionality. Specific examples of operably couplable include but are not limited to physically mateable and/or physically interacting components and/or wirelessly interactable and/or wirelessly interacting components and/or logically interacting and/or logically interactable components.


With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth herein for sake of clarity.


It will be understood by those within the art that, in general, terms used herein, and especially in the appended claims (e.g., bodies of the appended claims) are generally intended as “open” terms (e.g., the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” the term “includes” should be interpreted as “includes but is not limited to,” etc.). It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases “at least one” and “one or more” to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles “a” or “an” limits any particular claim containing such introduced claim recitation to inventions containing only one such recitation, even when the same claim includes the introductory phrases “one or more” or “at least one” and indefinite articles such as “a” or “an” (e.g., “a” and/or “an” should typically be interpreted to mean “at least one” or “one or more”); the same holds true for the use of definite articles used to introduce claim recitations. In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should typically be interpreted to mean at least the recited number (e.g., the bare recitation of “two recitations,” without other modifiers, typically means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to “at least one of A, B, and C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, and C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). In those instances where a convention analogous to “at least one of A, B, or C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, or C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that virtually any disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms. For example, the phrase “A or B” will be understood to include the possibilities of “A” or “B” or “A and B.” Further, unless otherwise noted, the use of the words “approximate,” “about,” “around,” “substantially,” etc., mean plus or minus ten percent.


The foregoing description of illustrative embodiments has been presented for purposes of illustration and of description. It is not intended to be exhaustive or limiting with respect to the precise form disclosed, and modifications and variations are possible in light of the above teachings or may be acquired from practice of the disclosed embodiments. It is intended that the scope of the invention be defined by the claims appended hereto and their equivalents.

Claims
  • 1. A magnetometer comprising: a light source configured to provide excitation light;a magneto-optical defect center material with at least one defect center that transmits emitted light when excited by the excitation light;a light sensor configured to receive the emitted light;a plurality of magnets configured to provide a bias magnetic field to the magneto-optical defect center material;a ring magnet holder comprising: an outer ring with an outside surface, anda plurality of holders extending from the ring, wherein the plurality of holders are configured to hold the plurality of magnets in a same orientation with respect to one another; anda mount comprising an inside surface, wherein the outside surface of the outer ring slides along the inside surface of the mount.
  • 2. The magnetometer of claim 1, further comprising a processor configured to: receive an indication of a frequency of the excitation light;receive an indication of a frequency of the emitted light; anddetermine a magnitude of an external magnetic field based at least in part on a comparison between the frequency of the excitation light and the frequency of the emitted light.
  • 3. The magnetometer of claim 2, wherein the processor is further configured to determine a direction of the external magnetic field based at least in part on a comparison between the frequency of the excitation light and the frequency of the emitted light.
  • 4. The magnetometer of claim 1, wherein the ring magnet holder further comprises a fixation member configured to secure the ring magnet holder in a location within the mount.
  • 5. The magnetometer of claim 4, wherein the fixation member comprises a set screw.
  • 6. The magnetometer of claim 1, wherein the mount comprises a through-hole configured to allow the excitation light to pass through the through-hole of the mount.
  • 7. The magnetometer of claim 1, wherein the inside surface of the mount has a shape that is semi-spherical.
  • 8. The magnetometer of claim 7, wherein the outside surface of the mount has a shape that is semi-spherical.
  • 9. The magnetometer of claim 1, wherein the mount comprises a first portion and a second portion that are secured together with a plurality of fasteners.
  • 10. The magnetometer of claim 9, wherein the first portion comprises half of the inside surface.
  • 11. The magnetometer of claim 1, wherein the plurality of magnets are permanent magnets.
  • 12. The magnetometer of claim 1, wherein the plurality of holders each comprise at least one magnet hole, wherein each of the at least one magnet hole is configured to hold one of the plurality of magnets.
  • 13. The magnetometer of claim 12, wherein the ring magnet holder further comprises at least one mounting tab, and wherein the at least one mounting tab comprises a fixation member configured to secure the ring magnet holder in a location within the mount.
  • 14. The magnetometer of claim 13, wherein the mounting tab further comprises at least one through-hole, wherein the at least one through-hole comprises a central axis that is coaxial to a central axis of one of the at least one magnet hole.
  • 15. The magnetometer of claim 1, wherein the bias magnetic field is substantially uniform through the magneto-optical defect center material.
  • 16. A device comprising: a plurality of magnets configured to provide a bias magnetic field to a magneto-optical defect center material;a ring magnet holder comprising: an outer ring with an outside surface, anda plurality of holders extending from the ring, wherein the plurality of holders are configured to hold a plurality of magnets in a same orientation with respect to one another; anda mount comprising an inside surface, wherein the outside surface of the outer ring slides along the inside surface of the mount.
  • 17. The device of claim 16, wherein the ring magnet holder further comprises a fixation member configured to secure the ring magnet holder in a location within the mount.
  • 18. The device of claim 17, wherein the fixation member comprises a set screw.
  • 19. The device of claim 16, wherein the mount comprises a through-hole configured to allow the excitation light to pass through the through-hole of the mount.
  • 20. The device of claim 16, wherein the inside surface of the mount has a shape that is semi-spherical.
  • 21. The device of claim 20, wherein the outside surface of the mount has a shape that is semi-spherical.
  • 22. The device of claim 16, wherein the mount comprises a first portion and a second portion that are secured together with a plurality of fasteners.
  • 23. The device of claim 22, wherein the first portion comprises half of the inside surface.
  • 24. The device of claim 16, wherein the plurality of magnets are permanent magnets.
  • 25. The device of claim 16, wherein the plurality of holders each comprise at least one magnet hole, wherein each of the at least one magnet hole is configured to hold one of the plurality of magnets.
  • 26. The device of claim 25, wherein the ring magnet holder further comprises at least one mounting tab, and wherein the at least one mounting tab comprises a fixation member configured to secure the ring magnet holder in a location within the mount.
  • 27. The device of claim 26, wherein the mounting tab further comprises at least one through-hole, wherein the at least one through-hole comprises a central axis that is coaxial to a central axis of one of the at least one magnet hole.
  • 28. A device for generating substantially uniform magnetic flux across a magneto-optical material, the device comprising: a magneto-optical material that is capable of fluorescing upon the application of certain light and that provides different fluorescence depending upon applied magnetic fields;a biasing magnet assembly comprising: an outer ring with an outside surface, anda plurality of holders extending from the ring, wherein the plurality of holders are configured to hold a plurality of magnets in a same orientation with respect to one another; anda mount comprising an inside surface, wherein the outside surface of the outer ring slides along the inside surface of the mount,wherein the biasing magnet assembly is adjustable to provide a uniform magnetic field to the magneto-optical material.
  • 29. The device of claim 28, wherein the biasing magnet assembly further comprises a fixation member configured to secure the ring magnet holder in a location within the mount.
  • 30. The device of claim 29, wherein the fixation member comprises a set screw.
  • 31. The device of claim 28, wherein the mount comprises a through-hole configured to allow the excitation light to pass through the through-hole of the mount.
  • 32. The device of claim 28, wherein the inside surface of the mount has a shape that is semi-spherical.
  • 33. The device of claim 32, wherein the outside surface of the mount has a shape that is semi-spherical.
  • 34. The device of claim 28, wherein the mount comprises a first portion and a second portion that are secured together with a plurality of fasteners.
  • 35. The device of claim 34, wherein the first portion comprises half of the inside surface.
  • 36. The device of claim 28, wherein the plurality of magnets are permanent magnets.
  • 37. The device of claim 28, wherein the plurality of holders each comprise at least one magnet hole, wherein each of the at least one magnet hole is configured to hold one of the plurality of magnets.
  • 38. The device of claim 37, wherein the ring magnet holder further comprises at least one mounting tab, and wherein the at least one mounting tab comprises a fixation member configured to secure the ring magnet holder in a location within the mount.
  • 39. The device of claim 38, wherein the mounting tab further comprises at least one through-hole, and wherein the at least one through-hole comprises a central axis that is coaxial to a central axis of one of the at least one magnet hole.
US Referenced Citations (435)
Number Name Date Kind
2746027 Murray May 1956 A
3359812 Everitt Dec 1967 A
3389333 Wolff et al. Jun 1968 A
3490032 Zurflueh Jan 1970 A
3514723 Cutler May 1970 A
3518531 Huggett Jun 1970 A
3621380 Barlow, Jr. Nov 1971 A
3745452 Osburn et al. Jul 1973 A
3899758 Maier et al. Aug 1975 A
4025873 Chilluffo May 1977 A
4047805 Sekimura Sep 1977 A
4078247 Albrecht Mar 1978 A
4084215 Willenbrock Apr 1978 A
4322769 Cooper Mar 1982 A
4329173 Culling May 1982 A
4359673 Bross et al. Nov 1982 A
4368430 Dale et al. Jan 1983 A
4410926 Hafner et al. Oct 1983 A
4437533 Bierkarre et al. Mar 1984 A
4514083 Fukuoka Apr 1985 A
4588993 Babij et al. May 1986 A
4636612 Cullen Jan 1987 A
4638324 Hannan Jan 1987 A
4675522 Arunkumar Jun 1987 A
4768962 Kupfer et al. Sep 1988 A
4818990 Fernandes Apr 1989 A
4820986 Mansfield et al. Apr 1989 A
4945305 Blood Jul 1990 A
4958328 Stubblefield Sep 1990 A
4982158 Nakata et al. Jan 1991 A
5019721 Martens et al. May 1991 A
5038103 Scarzello et al. Aug 1991 A
5113136 Hayashi et al. May 1992 A
5134369 Lo et al. Jul 1992 A
5189368 Chase Feb 1993 A
5200855 Meredith et al. Apr 1993 A
5210650 O'Brien et al. May 1993 A
5245347 Bonta et al. Sep 1993 A
5252912 Merritt et al. Oct 1993 A
5301096 Klontz et al. Apr 1994 A
5384109 Klaveness et al. Jan 1995 A
5396802 Moss Mar 1995 A
5420549 Prestage May 1995 A
5425179 Nickel et al. Jun 1995 A
5427915 Ribi et al. Jun 1995 A
5548279 Gaines Aug 1996 A
5568516 Strohallen et al. Oct 1996 A
5586069 Dockser Dec 1996 A
5597762 Popovici et al. Jan 1997 A
5638472 Van Delden Jun 1997 A
5694375 Woodall Dec 1997 A
5719497 Veeser et al. Feb 1998 A
5731996 Gilbert Mar 1998 A
5764061 Asakawa et al. Jun 1998 A
5818352 McClure Oct 1998 A
5846708 Hollis et al. Dec 1998 A
5888925 Smith et al. Mar 1999 A
5894220 Wellstood et al. Apr 1999 A
5907420 Chraplyvy et al. May 1999 A
5907907 Ohtomo et al. Jun 1999 A
5915061 Vanoli Jun 1999 A
5995696 Miyagi et al. Nov 1999 A
6042249 Spangenberg Mar 2000 A
6057684 Murakami et al. May 2000 A
6064210 Sinclair May 2000 A
6121053 Kolber et al. Sep 2000 A
6124862 Boyken et al. Sep 2000 A
6130753 Hopkins et al. Oct 2000 A
6144204 Sementchenko Nov 2000 A
6195231 Sedlmayr et al. Feb 2001 B1
6215303 Weinstock et al. Apr 2001 B1
6262574 Cho et al. Jul 2001 B1
6360173 Fullerton Mar 2002 B1
6398155 Hepner et al. Jun 2002 B1
6433944 Nagao et al. Aug 2002 B1
6437563 Simmonds et al. Aug 2002 B1
6472651 Ukai Oct 2002 B1
6472869 Upschulte et al. Oct 2002 B1
6504365 Kitamura Jan 2003 B2
6518747 Sager et al. Feb 2003 B2
6542242 Yost et al. Apr 2003 B1
6621377 Osadchy et al. Sep 2003 B2
6621578 Mizoguchi Sep 2003 B1
6636146 Wehoski Oct 2003 B1
6686696 Mearini et al. Feb 2004 B2
6690162 Schopohl et al. Feb 2004 B1
6765487 Holmes et al. Jul 2004 B1
6788722 Kennedy et al. Sep 2004 B1
6809829 Takata et al. Oct 2004 B1
7118657 Golovchenko et al. Oct 2006 B2
7221164 Barringer May 2007 B1
7277161 Claus Oct 2007 B2
7305869 Berman et al. Dec 2007 B1
7307416 Islam et al. Dec 2007 B2
7342399 Wiegert Mar 2008 B1
RE40343 Anderson May 2008 E
7400142 Greelish Jul 2008 B2
7413011 Chee et al. Aug 2008 B1
7427525 Santori et al. Sep 2008 B2
7448548 Compton Nov 2008 B1
7471805 Goldberg Dec 2008 B2
7474090 Islam et al. Jan 2009 B2
7543780 Marshall et al. Jun 2009 B1
7546000 Spillane et al. Jun 2009 B2
7570050 Sugiura Aug 2009 B2
7608820 Berman et al. Oct 2009 B1
7705599 Strack et al. Apr 2010 B2
7741936 Weller et al. Jun 2010 B1
7805030 Bratkovski et al. Sep 2010 B2
7868702 Ohnishi Jan 2011 B2
7889484 Choi Feb 2011 B2
7916489 Okuya Mar 2011 B2
7932718 Wiegert Apr 2011 B1
7983812 Potter Jul 2011 B2
8022693 Meyersweissflog Sep 2011 B2
8120351 Rettig et al. Feb 2012 B2
8120355 Stetson Feb 2012 B1
8124296 Fischel Feb 2012 B1
8138756 Barclay et al. Mar 2012 B2
8193808 Fu et al. Jun 2012 B2
8294306 Kumar et al. Oct 2012 B2
8310251 Orazem Nov 2012 B2
8311767 Stetson Nov 2012 B1
8334690 Kitching et al. Dec 2012 B2
8415640 Babinec et al. Apr 2013 B2
8471137 Adair et al. Jun 2013 B2
8480653 Birchard et al. Jul 2013 B2
8525516 Le Prado et al. Sep 2013 B2
8547090 Lukin et al. Oct 2013 B2
8574536 Boudou et al. Nov 2013 B2
8575929 Wiegert Nov 2013 B1
8686377 Twitchen et al. Apr 2014 B2
8704546 Konstantinov Apr 2014 B2
8758509 Twitchen et al. Jun 2014 B2
8803513 Hosek et al. Aug 2014 B2
8854839 Cheng et al. Oct 2014 B2
8885301 Heidmann Nov 2014 B1
8913900 Lukin et al. Dec 2014 B2
8933594 Kurs Jan 2015 B2
8947080 Lukin et al. Feb 2015 B2
8963488 Campanella et al. Feb 2015 B2
9103873 Martens et al. Aug 2015 B1
9157859 Walsworth et al. Oct 2015 B2
9245551 El Hallak et al. Jan 2016 B2
9249526 Twitchen et al. Feb 2016 B2
9270387 Wolfe et al. Feb 2016 B2
9291508 Biedermann et al. Mar 2016 B1
9317811 Scarsbrook Apr 2016 B2
9369182 Kurs et al. Jun 2016 B2
9442205 Geiser et al. Sep 2016 B2
9541610 Kaup et al. Jan 2017 B2
9551763 Hahn et al. Jan 2017 B1
9557391 Egan et al. Jan 2017 B2
9570793 Borodulin Feb 2017 B2
9590601 Krause et al. Mar 2017 B2
9614589 Russo et al. Apr 2017 B1
9632045 Englund et al. Apr 2017 B2
9645223 Megdal et al. May 2017 B2
9680338 Malpas et al. Jun 2017 B2
9689679 Budker et al. Jun 2017 B2
9720055 Hahn et al. Aug 2017 B1
9778329 Heidmann Oct 2017 B2
9779769 Heidmann Oct 2017 B2
9891297 Sushkov et al. Feb 2018 B2
20020144093 Inoue et al. Oct 2002 A1
20020167306 Zalunardo et al. Nov 2002 A1
20030058346 Bechtel et al. Mar 2003 A1
20030076229 Blanpain et al. Apr 2003 A1
20030094942 Friend et al. May 2003 A1
20030098455 Amin et al. May 2003 A1
20030235136 Akselrod et al. Dec 2003 A1
20040013180 Giannakis et al. Jan 2004 A1
20040022179 Giannakis et al. Feb 2004 A1
20040042150 Swinbanks et al. Mar 2004 A1
20040081033 Arieli et al. Apr 2004 A1
20040095133 Nikitin et al. May 2004 A1
20040109328 Dahl et al. Jun 2004 A1
20040247145 Luo et al. Dec 2004 A1
20050031840 Swift et al. Feb 2005 A1
20050068249 Frederick Du Toit et al. Mar 2005 A1
20050099177 Greelish May 2005 A1
20050112594 Grossman May 2005 A1
20050126905 Golovchenko et al. Jun 2005 A1
20050130601 Palermo et al. Jun 2005 A1
20050134257 Etherington et al. Jun 2005 A1
20050138330 Owens et al. Jun 2005 A1
20050146327 Jakab Jul 2005 A1
20060012385 Tsao et al. Jan 2006 A1
20060054789 Miyamoto et al. Mar 2006 A1
20060055584 Waite et al. Mar 2006 A1
20060062084 Drew Mar 2006 A1
20060071709 Maloberti et al. Apr 2006 A1
20060245078 Kawamura Nov 2006 A1
20060247847 Carter et al. Nov 2006 A1
20060255801 Ikeda Nov 2006 A1
20060291771 Braunisch et al. Dec 2006 A1
20070004371 Okanobu Jan 2007 A1
20070120563 Kawabata et al. May 2007 A1
20070247147 Xiang et al. Oct 2007 A1
20070273877 Kawano et al. Nov 2007 A1
20080016677 Creighton, IV Jan 2008 A1
20080048640 Hull et al. Feb 2008 A1
20080078233 Larson et al. Apr 2008 A1
20080089367 Srinivasan et al. Apr 2008 A1
20080204004 Anderson Aug 2008 A1
20080217516 Suzuki et al. Sep 2008 A1
20080239265 Den Boef Oct 2008 A1
20080253264 Nagatomi et al. Oct 2008 A1
20080265895 Strack et al. Oct 2008 A1
20080266050 Crouse et al. Oct 2008 A1
20080279047 An et al. Nov 2008 A1
20080299904 Yi et al. Dec 2008 A1
20090001979 Kawabata Jan 2009 A1
20090015262 Strack et al. Jan 2009 A1
20090042592 Cho et al. Feb 2009 A1
20090058697 Aas et al. Mar 2009 A1
20090060790 Okaguchi et al. Mar 2009 A1
20090079417 Mort et al. Mar 2009 A1
20090079426 Anderson Mar 2009 A1
20090132100 Shibata May 2009 A1
20090157331 Van Netten Jun 2009 A1
20090161264 Meyersweissflog Jun 2009 A1
20090195244 Mouget et al. Aug 2009 A1
20090222208 Speck Sep 2009 A1
20090243616 Loehken et al. Oct 2009 A1
20090244857 Tanaka Oct 2009 A1
20090277702 Kanada et al. Nov 2009 A1
20090310650 Chester et al. Dec 2009 A1
20100004802 Bodin et al. Jan 2010 A1
20100015438 Williams et al. Jan 2010 A1
20100015918 Liu et al. Jan 2010 A1
20100045269 Lafranchise et al. Feb 2010 A1
20100071904 Burns et al. Mar 2010 A1
20100102809 May Apr 2010 A1
20100102820 Martinez et al. Apr 2010 A1
20100134922 Yamada et al. Jun 2010 A1
20100157305 Henderson Jun 2010 A1
20100188081 Lammegger Jul 2010 A1
20100237149 Olmstead Sep 2010 A1
20100271016 Barclay et al. Oct 2010 A1
20100271032 Helwig Oct 2010 A1
20100277121 Hall et al. Nov 2010 A1
20100308813 Lukin et al. Dec 2010 A1
20100315079 Lukin Dec 2010 A1
20100321117 Gan Dec 2010 A1
20100326042 McLean et al. Dec 2010 A1
20110031969 Kitching et al. Feb 2011 A1
20110034393 Justen et al. Feb 2011 A1
20110059704 Norimatsu et al. Mar 2011 A1
20110062957 Fu et al. Mar 2011 A1
20110062967 Mohaupt Mar 2011 A1
20110066379 Mes Mar 2011 A1
20110120890 MacPherson et al. May 2011 A1
20110127999 Lott et al. Jun 2011 A1
20110165862 Yu et al. Jul 2011 A1
20110175604 Polzer et al. Jul 2011 A1
20110176563 Friel et al. Jul 2011 A1
20110243267 Won et al. Oct 2011 A1
20110270078 Wagenaar et al. Nov 2011 A1
20110279120 Sudow et al. Nov 2011 A1
20110315988 Yu et al. Dec 2011 A1
20120016538 Waite et al. Jan 2012 A1
20120019242 Hollenberg et al. Jan 2012 A1
20120037803 Strickland Feb 2012 A1
20120044014 Stratakos et al. Feb 2012 A1
20120051996 Scarsbrook et al. Mar 2012 A1
20120063505 Okamura et al. Mar 2012 A1
20120087449 Ling et al. Apr 2012 A1
20120089299 Breed Apr 2012 A1
20120140219 Cleary Jun 2012 A1
20120181020 Barron et al. Jul 2012 A1
20120194068 Cheng et al. Aug 2012 A1
20120203086 Rorabaugh et al. Aug 2012 A1
20120232838 Kemppi et al. Sep 2012 A1
20120235633 Kesler et al. Sep 2012 A1
20120235634 Hall et al. Sep 2012 A1
20120245885 Kimishima Sep 2012 A1
20120257683 Schwager et al. Oct 2012 A1
20120281843 Christensen et al. Nov 2012 A1
20120326793 Gan Dec 2012 A1
20130043863 Ausserlechner et al. Feb 2013 A1
20130070252 Feth Mar 2013 A1
20130093424 Blank et al. Apr 2013 A1
20130107253 Santori May 2013 A1
20130127518 Nakao May 2013 A1
20130179074 Haverinen Jul 2013 A1
20130215712 Geiser et al. Aug 2013 A1
20130223805 Ouyang et al. Aug 2013 A1
20130265042 Kawabata et al. Oct 2013 A1
20130265782 Barrena et al. Oct 2013 A1
20130270991 Twitchen et al. Oct 2013 A1
20130279319 Matozaki et al. Oct 2013 A1
20130292472 Guha Nov 2013 A1
20140012505 Smith et al. Jan 2014 A1
20140015522 Widmer et al. Jan 2014 A1
20140037932 Twitchen et al. Feb 2014 A1
20140044208 Woodsum Feb 2014 A1
20140061510 Twitchen et al. Mar 2014 A1
20140070622 Keeling et al. Mar 2014 A1
20140072008 Faraon et al. Mar 2014 A1
20140077231 Twitchen et al. Mar 2014 A1
20140081592 Bellusci et al. Mar 2014 A1
20140104008 Gan Apr 2014 A1
20140126334 Megdal et al. May 2014 A1
20140139322 Wang et al. May 2014 A1
20140153363 Juhasz et al. Jun 2014 A1
20140154792 Moynihan et al. Jun 2014 A1
20140159652 Hall et al. Jun 2014 A1
20140166904 Walsworth et al. Jun 2014 A1
20140167759 Pines et al. Jun 2014 A1
20140168174 Idzik et al. Jun 2014 A1
20140180627 Naguib et al. Jun 2014 A1
20140191139 Englund Jul 2014 A1
20140191752 Walsworth et al. Jul 2014 A1
20140197831 Walsworth Jul 2014 A1
20140198463 Klein Jul 2014 A1
20140210473 Campbell et al. Jul 2014 A1
20140215985 Pollklas Aug 2014 A1
20140225606 Endo et al. Aug 2014 A1
20140247094 Englund et al. Sep 2014 A1
20140264723 Liang et al. Sep 2014 A1
20140265555 Hall et al. Sep 2014 A1
20140272119 Kushalappa et al. Sep 2014 A1
20140273826 Want et al. Sep 2014 A1
20140291490 Hanson et al. Oct 2014 A1
20140297067 Malay Oct 2014 A1
20140306707 Walsworth et al. Oct 2014 A1
20140327439 Cappellaro et al. Nov 2014 A1
20140335339 Dhillon et al. Nov 2014 A1
20140340085 Cappellaro et al. Nov 2014 A1
20140368191 Goroshevskiy et al. Dec 2014 A1
20150001422 Englund et al. Jan 2015 A1
20150009746 Kucsko et al. Jan 2015 A1
20150015247 Goodwill et al. Jan 2015 A1
20150018018 Shen et al. Jan 2015 A1
20150022404 Chen et al. Jan 2015 A1
20150048822 Walsworth et al. Feb 2015 A1
20150054355 Ben-Shalom et al. Feb 2015 A1
20150061590 Widmer et al. Mar 2015 A1
20150061670 Fordham et al. Mar 2015 A1
20150090033 Budker et al. Apr 2015 A1
20150128431 Kuo May 2015 A1
20150137793 Englund et al. May 2015 A1
20150153151 Kochanski Jun 2015 A1
20150192532 Clevenson et al. Jul 2015 A1
20150192596 Englund et al. Jul 2015 A1
20150225052 Cordell Aug 2015 A1
20150235661 Heidmann Aug 2015 A1
20150253355 Grinolds et al. Sep 2015 A1
20150268373 Meyer Sep 2015 A1
20150269957 El Hallak et al. Sep 2015 A1
20150276897 Leussler et al. Oct 2015 A1
20150288352 Krause et al. Oct 2015 A1
20150299894 Markham et al. Oct 2015 A1
20150303333 Yu et al. Oct 2015 A1
20150314870 Davies Nov 2015 A1
20150326030 Malpas et al. Nov 2015 A1
20150326410 Krause et al. Nov 2015 A1
20150354985 Judkins et al. Dec 2015 A1
20150358026 Gan Dec 2015 A1
20150374250 Hatano et al. Dec 2015 A1
20150377865 Acosta et al. Dec 2015 A1
20150377987 Menon et al. Dec 2015 A1
20160018269 Maurer et al. Jan 2016 A1
20160031339 Geo Feb 2016 A1
20160036529 Griffith et al. Feb 2016 A1
20160052789 Gaathon et al. Feb 2016 A1
20160054402 Meriles Feb 2016 A1
20160061914 Jelezko Mar 2016 A1
20160071532 Heidmann Mar 2016 A9
20160077167 Heidmann Mar 2016 A1
20160097702 Zhao et al. Apr 2016 A1
20160113507 Reza et al. Apr 2016 A1
20160131723 Nagasaka May 2016 A1
20160139048 Heidmann May 2016 A1
20160146904 Stetson, Jr. et al. May 2016 A1
20160161429 Englund et al. Jun 2016 A1
20160161583 Meriles et al. Jun 2016 A1
20160174867 Hatano Jun 2016 A1
20160214714 Sekelsky Jul 2016 A1
20160216304 Sekelsky Jul 2016 A1
20160216340 Egan et al. Jul 2016 A1
20160216341 Boesch et al. Jul 2016 A1
20160221441 Hall et al. Aug 2016 A1
20160223621 Kaup et al. Aug 2016 A1
20160231394 Manickam et al. Aug 2016 A1
20160266220 Sushkov et al. Sep 2016 A1
20160282427 Heidmann Sep 2016 A1
20160291191 Fukushima et al. Oct 2016 A1
20160313408 Hatano et al. Oct 2016 A1
20160348277 Markham et al. Dec 2016 A1
20160356863 Boesch et al. Dec 2016 A1
20170010214 Osawa et al. Jan 2017 A1
20170010334 Krause et al. Jan 2017 A1
20170010338 Bayat et al. Jan 2017 A1
20170010594 Kottapalli et al. Jan 2017 A1
20170023487 Boesch Jan 2017 A1
20170030982 Jeske et al. Feb 2017 A1
20170038314 Suyama et al. Feb 2017 A1
20170038411 Yacobi et al. Feb 2017 A1
20170068012 Fisk Mar 2017 A1
20170074660 Gann et al. Mar 2017 A1
20170075020 Gann et al. Mar 2017 A1
20170075205 Kriman et al. Mar 2017 A1
20170077665 Liu et al. Mar 2017 A1
20170104426 Mills Apr 2017 A1
20170138735 Cappellaro et al. May 2017 A1
20170139017 Egan et al. May 2017 A1
20170146615 Wolf et al. May 2017 A1
20170199156 Villani et al. Jul 2017 A1
20170205526 Meyer Jul 2017 A1
20170207823 Russo et al. Jul 2017 A1
20170211947 Fisk Jul 2017 A1
20170212046 Cammerata Jul 2017 A1
20170212177 Coar et al. Jul 2017 A1
20170212178 Hahn et al. Jul 2017 A1
20170212179 Hahn et al. Jul 2017 A1
20170212180 Hahn et al. Jul 2017 A1
20170212181 Coar et al. Jul 2017 A1
20170212182 Hahn et al. Jul 2017 A1
20170212183 Egan et al. Jul 2017 A1
20170212184 Coar et al. Jul 2017 A1
20170212185 Hahn et al. Jul 2017 A1
20170212186 Hahn et al. Jul 2017 A1
20170212187 Hahn et al. Jul 2017 A1
20170212190 Reynolds et al. Jul 2017 A1
20170212258 Fisk Jul 2017 A1
20170261629 Gunnarsson et al. Sep 2017 A1
20170343617 Manickam et al. Nov 2017 A1
20170343619 Manickam et al. Nov 2017 A1
20170343621 Hahn et al. Nov 2017 A1
20170343695 Stetson et al. Nov 2017 A1
20180136291 Pham May 2018 A1
20180275209 Mandeville et al. Sep 2018 A1
20180275212 Hahn et al. Sep 2018 A1
Foreign Referenced Citations (105)
Number Date Country
105738845 Jul 2016 CN
106257602 Dec 2016 CN
69608006 Feb 2001 DE
19600241 Aug 2002 DE
10228536 Jan 2003 DE
0 161 940 Dec 1990 EP
0 718 642 Jun 1996 EP
0 726 458 Aug 1996 EP
1 505 627 Feb 2005 EP
1 685 597 Aug 2006 EP
1 990 313 Nov 2008 EP
2 163 392 Mar 2010 EP
2 495 166 Sep 2012 EP
2 587 232 May 2013 EP
2 705 179 Mar 2014 EP
2 707 523 Mar 2014 EP
2 745 360 Jun 2014 EP
2 769 417 Aug 2014 EP
2 790 031 Oct 2014 EP
2 837 930 Feb 2015 EP
2 907 792 Aug 2015 EP
2 423 366 Aug 2006 GB
2 433 737 Jul 2007 GB
2 482 596 Feb 2012 GB
2 483 767 Mar 2012 GB
2 486 794 Jun 2012 GB
2 490 589 Nov 2012 GB
2 491 936 Dec 2012 GB
2 493 236 Jan 2013 GB
2 495 632 Apr 2013 GB
2 497 660 Jun 2013 GB
2 510 053 Jul 2014 GB
2 515 226 Dec 2014 GB
2 522 309 Jul 2015 GB
2 526 639 Dec 2015 GB
3782147 Jun 2006 JP
4800896 Oct 2011 JP
2012-103171 May 2012 JP
2012-110489 Jun 2012 JP
2012-121748 Jun 2012 JP
2013-028497 Feb 2013 JP
5476206 Apr 2014 JP
5522606 Jun 2014 JP
5536056 Jul 2014 JP
5601183 Oct 2014 JP
2014-215985 Nov 2014 JP
2014-216596 Nov 2014 JP
2015-518562 Jul 2015 JP
5764059 Aug 2015 JP
2015-167176 Sep 2015 JP
2015-529328 Oct 2015 JP
5828036 Dec 2015 JP
5831947 Dec 2015 JP
WO-8704028 Jul 1987 WO
WO-8804032 Jun 1988 WO
WO-9533972 Dec 1995 WO
WO-2009073736 Jun 2009 WO
WO-2011046403 Apr 2011 WO
WO-2011153339 Dec 2011 WO
WO-2012016977 Feb 2012 WO
WO-2012084750 Jun 2012 WO
WO-2013027074 Feb 2013 WO
WO-2013059404 Apr 2013 WO
WO-2013066446 May 2013 WO
WO-2013066448 May 2013 WO
WO-2013093136 Jun 2013 WO
WO-2013188732 Dec 2013 WO
WO-2013190329 Dec 2013 WO
WO-2014011286 Jan 2014 WO
WO-2014099110 Jun 2014 WO
WO-2014135544 Sep 2014 WO
WO-2014135547 Sep 2014 WO
WO-2014166883 Oct 2014 WO
WO-2014210486 Dec 2014 WO
WO-2015015172 Feb 2015 WO
WO-2015142945 Sep 2015 WO
WO-2015157110 Oct 2015 WO
WO-2015157290 Oct 2015 WO
WO-2015158383 Oct 2015 WO
WO-2015193156 Dec 2015 WO
WO-2016075226 May 2016 WO
WO-2016118756 Jul 2016 WO
WO-2016118791 Jul 2016 WO
WO-2016122965 Aug 2016 WO
WO-2016122966 Aug 2016 WO
WO-2016126435 Aug 2016 WO
WO-2016126436 Aug 2016 WO
WO-2016190909 Dec 2016 WO
WO-2017007513 Jan 2017 WO
WO-2017007514 Jan 2017 WO
WO-2017014807 Jan 2017 WO
WO-2017039747 Mar 2017 WO
WO-2017095454 Jun 2017 WO
WO-2017127079 Jul 2017 WO
WO-2017127080 Jul 2017 WO
WO-2017127081 Jul 2017 WO
WO-2017127085 Jul 2017 WO
WO-2017127090 Jul 2017 WO
WO-2017127091 Jul 2017 WO
WO-2017127093 Jul 2017 WO
WO-2017127094 Jul 2017 WO
WO-2017127095 Jul 2017 WO
WO-2017127096 Jul 2017 WO
WO-2017127097 Jul 2017 WO
WO-2017127098 Jul 2017 WO
Non-Patent Literature Citations (406)
Entry
U.S. Notice of Allowance dated Oct. 19, 2017, from related U.S. Appl. No. 15/179,957, 5 pages.
U.S. Notice of Allowance dated Oct. 23, 2017, from related U.S. Appl. No. 15/003,797, 6 pages.
U.S. Office Action dated Nov. 24, 2017, from related U.S. Appl. No. 15/003,145, 14 pages.
U.S. Office Action dated Nov. 27, 2017, from related U.S. Appl. No. 15/468,386, 28 pages.
Teeling-Smith et al., “Electron Paramagnetic Resonance of a Single NV Nanodiamond Attached to an Individual Biomolecule”, Biophysical Journal 110, May 10, 2016, pp. 2044-2052.
UK Office Action dated Jun. 8, 2018, from related application No. GB1617438.5, 3 pages.
U.S. Final Office Action dated Jul. 26, 2018 from related U.S. Appl. No. 15/003,177, 14 pages.
U.S. Non-Final Office Action dated Aug. 6, 2018 from related U.S. Appl. No. 15/376,244, 28 pages.
U.S. Non-Final Office Action dated Aug. 9, 2018 from related U.S. Appl. No. 15/003,309, 22 pages.
U.S. Non-Final Office Action dated Jul. 20, 2018 from related U.S. Appl. No. 15/350,303, 13 pages.
U.S. Non-Final Office Action dated Jul. 26, 2018 from related U.S. Appl. No. 15/380,419, 11 pages.
U.S. Non-Final Office Action dated Jul. 3, 2018 from related U.S. Appl. No. 15/003,396, 19 pages.
U.S. Notice of Allowance dated Jul. 18, 2018 from related U.S. Appl. No. 15/468,386, 12 pages.
U.S. Notice of Allowance dated Jul. 6, 2018 from related U.S. Appl. No. 15/672,953, 11 pages.
U.S. Notice of Allowance dated Jun. 27, 2018 from related U.S. Appl. No. 15/003,519, 21 pages.
U.S. Notice of Allowance dated May 15, 2018, from related U.S. Appl. No. 15/003,209, 7 pages.
U.S. Notice of Allowance dated May 16, 2018, from related U.S. Appl. No. 15/003,145, 8 pages.
U.S. Office Action dated Jun. 19, 2018, from related U.S. Appl. No. 15/450,504, 12 pages.
“'Diamond Sensors, Detectors, and Quantum Devices' in Patent Application Approval Process,” Chemicals & Chemistry, pp. 1-6, (Feb. 28, 2014), 6 pages.
“Findings from University of Stuttgart in physics reported,” Science Letter, (Jul. 7, 2009), 2 pages.
“New Findings on Nitrogen from Ecole Normale Superieure Summarized (Magnetic imaging with an ensemble of nitrogen vacancy-centers in diamond),” Physics Week, pp. 1-2, (Jul. 21, 2015), 2 pages.
“Patent Issued for Diamond Sensors, Detectors, and Quantum Devices (U.S. Pat. No. 9,249,526),” Journal of Engineering, pp. 1-5 (Feb. 15, 2016), 5 pages.
“Researchers Submit Patent Application, ‘Diamond Sensors, Detectors, and Quantum Devices’, for Approval,” Chemicals & Chemistry, pp. 1-7, (Apr. 11, 2014), 7 pages.
Acosta et al., “Broadband magnetometry by infrared-absorption detection of nitrogen-vacancy ensembles in diamond,” Appl. Phys. Letters 97: 174104 (Oct. 29, 2010), 4 pages.
Acosta et al., “Diamonds with a high density of nitrogen-vacancy centers for magnetometry applications,” Physical Review B 80(115202): 1-15 (Sep. 9, 2009), 15 pages.
Acosta et al., “Nitrogen-vacancy centers: physics and applications,” MRS Bulletin 38(2): 127-130 (Feb. 2013), 4 pages.
Acosta, “Optical Magnetometry with Nitrogen-Vacancy Centers in Diamond,” University of California Berkeley, (Spring 2011), 118 pages.
Aiello et al., “Composite-pulse magnetometry with a solid-state quantum sensor,” Nature Communications 4(1419): 1-6 (Jan. 29, 2013), 6 pages.
Alam, “Solid-state 13C magic angle spinning NMR spectroscopy characterization of particle size structural variations in synthetic nanodiamonds,” Materials Chemistry and Physics 85(2-3): 310-315 (Jun. 15, 2004), 6 pages.
Albrecht et al., “Coupling of nitrogen vacancy centres in nanodiamonds by means of phonons,” New Journal of Physics 15(083014): 1-26 (Aug. 6, 2013), 27 pages.
Appel et al., “Nanoscale microwave imaging with a single electron spin in diamond,” New Journal of Physics 17(112001): 1-6 (Nov. 3, 2015), 7 pages.
Arai et al., “Fourier magnetic imaging with nanoscale resolution and compressed sensing speed-up using electronic spins in diamond,” Nature Nanotechnology 10: 859-864 (Aug. 10, 2015), 7 pages.
Aslam et al., “Single spin optically detected magnetic resonance with 60-90 GHz (E-band) microwave resonators,” Review of Scientific Instruments 86(064704): 1-8 (Jun. 22, 2015), 9 pages.
Awschalom et al., “Diamond age of spintronics,” Scientific American 297: 84-91 (Oct. 2007), 8 pages.
Babamoradi et al., “Correlation between entanglement and spin density in nitrogen-vacancy center of diamond,” European Physical Journal D 65: 597-603 (Dec. 1, 2011), 7 pages.
Babunts et al., “Diagnostics of NV defect structure orientation in diamond using optically detected magnetic resonance with a modulated magnetic field,” Technical Physics Letters 41(6): 583-586 (Jun. 2015; first published online Jul. 14, 2015), 4 pages.
Babunts et al., “Temperature-scanned magnetic resonance and the evidence of two-way transfer of a nitrogen nuclear spin hyperfine interaction in coupled NV—N pairs in diamond,” JETP Letters 95(8): 429-432 (Jun. 27, 2012), 4 pages.
Bagguley et al., “Zeeman effect of acceptor states in semiconducting diamond,” Journal of the Physical Society of Japan 21(Supplement): 244-248 (1966), 7 pages.
Balasubramanian et al., “Nanoscale imaging magnetometry with diamond spins under ambient conditions,” Nature 455: 648-651 (Oct. 2, 2008), 5 pages.
Balmer et al., “Chemical Vapour deposition synthetic diamond: materials technology and applications,” J. of Physics: Condensed Matter 21(36): 1-51 (Aug. 19, 2009), 51 pages.
Baranov et al., “Enormously High Concentrations of Fluorescent Nitrogen-Vacancy Centers Fabricated by Sintering of Detonation Nanodiamonds,” Small 7(11): 1533-1537 (Jun. 6, 2011; first published online Apr. 26, 2011), 5 pages.
Barfuss et al., “Strong mechanical driving of a single electron spin,” Nature Physics 11: 820-824 (Aug. 3, 2015), 6 pages.
Barry et al., “Optical magnetic detection of single-neuron action potentials using quantum defects in diamond,” as submitted to Quantum Physics on Feb. 2, 2016, 23 pages.
Bennett et al., “CVD Diamond for High Power Laser Applications,” SPIE 8603, High-Power Laser Materials Processing: Lasers, Beam Delivery, Diagnostics, and Applications II, 860307 (Feb. 22, 2013), 10 pages.
Berman & Chernobrod, “Single-spin microscope with sub-nanoscale resolution based on optically detected magnetic resonance,” SPIE 7608, Quantum Sensing and Nanophotonic Devices VII, 76080Y (Jan. 23, 2010), 4 pages.
Berman et al. “Measurement of single electron and nuclear spin states based on optically detected magnetic resonance,” J. Physics: Conf. Series 38: 167-170 (2006), 5 pages.
Blakley et al., “Room-temperature magnetic gradiometry with fiber-coupled nitrogen-vacancy centers in diamond,” Optics Letters 40(16): 3727-3730 (Aug. 5, 2015), 4 pages.
Bourgeois, et al., “Photoelectric detection of electron spin resonance of nitrogen-vacancy centres in diamond,” Nature Communications 6(8577): 1-8 (Oct. 21, 2015), 8 pages.
Brenneis, et al. “Ultrafast electronic readout of diamond nitrogen-vacancy centres coupled to graphene.” Nature nanotechnology 10.2 (2015): 135-139.
Bucher et al, “High Resolution Magnetic Resonance Spectroscopy Using Solid-State Spins”, May 25, 2017, downloaded from https://arxiv.org/ (arXiv.org > quant-ph > arXiv:1705.08887) on May 25, 2017, pp. 1-24.
Budker & Kimball, “Optical Magnetometry,” Cambridge Press, (2013), 11 pages.
Budker & Romalis, “Optical Magnetometry,” Nature Physics 3: 227-243 (Apr. 2007), 8 pages.
Casanova, et al., “Effect of magnetic field on phosphorus centre in diamond,” Physica Status Solidi A 186(2): 291-295 (Jul. 30, 2001), 6 pages.
Castelletto, et al., “Frontiers in diffraction unlimited optical methods for spin manipulation, magnetic field sensing and imaging using diamond nitrogen vacancy defects,” Nanophotonics 1(2): 139-153 (Nov. 2012), 15 pages.
Chapman, et al., “Anomalous saturation effects due to optical spin depolarization in nitrogen-vacancy centers in diamond nanocrystals,” Physical Review B 86(045204): 1-8 (Jul. 10, 2012), 8 pages.
Chavez, et al. “Detecting Arctic oil spills with NMR: a feasibility study.” Near Surface Geophysics 13.4 (Feb. 2015): 409-416.
Chen et al., “Vector magnetic field sensing by a single nitrogen vacancy center in diamond,” EPL 101(67003): 1-5 (Mar. 2013), 6 pages.
Chernobrod et al., “Improving the sensitivity of frequency modulation spectroscopy using nanomechanical cantilevers,” Applied Physics Letters 85(17): 3896-3898 (Oct. 25, 2004), 3 pages.
Chernobrod et al., “Spin Microscope Based on Optically Detected Magnetic Resoncance,” Journal of Applied Physics 97(014903): 1-3, (2005; first published online Dec. 10, 2004), 4 pages.
Childress et al., “Coherent dynamics of coupled electron and nuclear spin qubits in diamond,” Science 314(5797): 281-285 (Oct. 13, 2006), 6 pages.
Chipaux et al., “Magnetic imaging with an ensemble of nitrogen vacancy-centers in diamond,” European Physical Journal D 69(166): 1-10 (Jul. 2, 2015), 10 pages.
Chipaux et al., “Nitrogen vacancies (NV) centers in diamond for magnetic sensors and quantum sensing,” SPIE 9370, Quantum Sensing and Nanophotonic Devices XII, 93701V (Feb. 8, 2015), 6 pages.
Chipaux, et al., “Wide bandwidth instantaneous radio frequency spectrum analyzer based on nitrogen vacancy centers in diamond,” Applied Physics Letters 107(233502): 1-5 (2015), 6 pages.
Clevenson et al., “Broadband magnetometry and temperature sensing with a light-trapping diamond waveguide,” Nature Physics 11: 393-397 (May 2015; first published online Apr. 6, 2015), 6 pages.
Constable, “Geomagnetic Spectrum, Temporal.” In Encyclopedia of Geomagnetism and Paleomagnetism, pp. 353-355, Springer: Dordrecht, Netherlands (2007), 3 pages.
Cooper et al., “Time-resolved magnetic sensing with electronic spins in diamond,” Nature Communications 5:3141: 1-7 (Jan. 24, 2014), 7 pages.
Creedon et al., “Strong coupling between P1 diamond impurity centers and a three-dimensional lumped photonic microwave cavity,” Physical Review B 91(140408R): 1-5 (Apr. 24, 2015), 5 pages.
Dale, et al. “Medical applications of diamond magnetometry: commercial viability.” arXiv preprint arXiv:1705.01994 (May 8, 2017), pp. 1-7.
Davies, “Current problems in diamond: towards a quantitative understanding,” Physica B 273-274: 15-13 (Dec. 15, 1999), 9 pages.
De Lange et al., “Single-Spin Magnetometry with Multipulse Sensing Sequences,” Physical Review Letters 106(080802): 1-4 (Feb. 24, 2011), 4 pages.
Degen, “Scanning magnetic field microscope with a diamond single-spin sensor,” Applied Physics Letters 92(243111): 1-3 (Jun. 17, 2008), 3 pages.
Delacroix et al., “Design, manufacturing, and performance analysis of mid-infrared achromatic half-wave plates with diamond subwavelength gratings,” Applied Optics 51(24): 5897-5902 (Aug. 16, 2012), 6 pages.
Denatale et al., “Fabrication and characterization of diamond moth eye antireflective surfaces on Ge,” J. of Applied Physics 71: 1388-1393 (Mar. 1992), 8 pages.
Dobrovitski et al., “Quantum Control over Single Spins in Diamond,” Annual Review of Condensed Matter Physics 4: 23-50 (Apr. 2013), 30 pages.
Doherty et al., “The nitrogen-vacancy colour centre in diamond,” Physics Reports 528: 1-45 (Jul. 1, 2013), 45 pages.
Doherty et al., “Theory of the ground-state spin of the NV-center in diamond,” Physical Review B 85(205203): 1-21 (May 3, 2012), 21 pages.
Doi et al., “Pure negatively charged state of the NV center in n-type diamond,” Physical Review B 93(081203): 1-6 (Feb. 3, 2016), 6 pages.
Drake et al., “Influence of magnetic field alignment and defect concentration on nitrogen-vacancy polarization in diamond,” New Journal of Physics 18(013011): 1-8 (Jan. 2016; first published on Dec. 24, 2015), 9 pages.
Dreau et al., “Avoiding power broadening in optically detected magnetic resonance of single NV defects for enhanced dc magnetic field sensitivity,” Physical Review B 84(195204): 1-8 (Nov. 23, 2011), 8 pages.
Dreau et al., “High-resolution spectroscopy of single NV defects coupled with nearby 13C nuclear spins in diamond,” Physical Review B 85(134107): 1-7 (Apr. 20, 2012), 7 pages.
Dumeige et al., “Magnetometry with nitrogen-vacancy ensembles in diamond based on infrared absorption in a doubly resonant optical cavity,” Physical Review B 87(155202): 1-9 (Apr. 8, 2013), 9 pages.
Epstein et al., “Anisotropic interactions of a single spin and dark-spin spectroscopy in diamond,” Nature Physics 1:94-98 (Nov. 2005), 5 pages.
Fallah et al., “Multi-sensor approach in vessel magnetic wake imaging,” Wave Motion 51(1): 60-76 (Jan. 2014), retrieved from http://www.sciencedirect.com/science/article/pii/S0165212513001133 (Aug. 21, 2016).
Fedotov et al., “High-resolution magnetic field imaging with a nitrogen-vacancy diamond sensor integrated with a photonic-crystal fiber,” Optics Letters 41(3): 472-475 (Feb. 1, 2016; published Jan. 25, 2016), 4 pages.
Fedotov et al., “Photonic-crystal-fiber-coupled photoluminescence interrogation of nitrogen vacancies in diamond nanoparticles,” Laser Physics Letters 9(2): 151-154 (Feb. 2012; first published online Dec. 2, 2011), 5 pages.
Feng & Wei, “A steady-state spectral method to fit microwave absorptions of NV centers in diamonds: application to sensitive magnetic field sensing,” Measurement Science & Technology 25(105102): 1-6 (Oct. 2014; first published online Aug. 29, 2014), 7 pages.
Fologea, et al. “Detecting single stranded DNA with a solid state nanopore.” Nano Letters 5.10 (Aug. 15, 2005): 1905-1909.
Freitas, et al., “Solid-State Nuclear Magnetic Resonance (NMR) Methods Applied to the Study of Carbon Materials,” Chemistry and Physics of Carbon, vol. 31 (2012), 45 pages.
Gaebel, et al. “Room-temperature coherent coupling of single spins in diamond.” Nature Physics 2.6 (May 28, 2006): 408-413.
GB Examination Report from United Kingdom application No. GB 1618202.4 dated Jan. 10, 2017.
Geiselmann et al., “Fast optical modulation of the fluorescence from a single nitrogen-vacancy centre,” Nature Physics 9: 785-789 (Dec. 2013; first published online Oct. 13, 2013), 5 pages.
Gombert & Blasi, “The Moth-Eye Effect—From Fundamentals to Commercial Exploitation,” Functional Properties of Bio-Inspired Surfaces: 79-102, (Nov. 2009), 26 pages.
Gong et al., “Generation of Nitrogen-Vacancy Center Pairs in Bulk Diamond by Molecular Nitrogen Implantation,” Chinese Physics Letters 33(2)(026105): 1-4 (Feb. 2016), 5 pages.
Gould et al., “An imaging magnetometer for bio-sensing based on nitrogen-vacancy centers in diamond,” SPIE 8933, Frontiers in Biological Detection: From Nanosensors to Systems VI, 89330L (Mar. 18, 2014), 8 pages.
Gould et al., “Room-temperature detection of a single 19 nm superparamagnetic nanoparticle with an imaging magnetometer,” Applied Physics Letters 105(072406): 1-4 (Aug. 19, 2014), 5 pages.
Gruber et al., “Scanning confocal optical microscopy and magnetic resonance on single defect centers,” Science 276(5321): 2012-2014 (Jun. 27, 1997), 4 pages.
Haeberle et al., “Nanoscale nuclear magnetic imaging with chemical contrast,” Nature Nanotechnology 10: 125-128 (Feb. 2015; first published online Jan. 5, 2015), 4 pages.
Haihua et al., “Design of wideband anti-reflective sub wavelength nanostructures,” Infrared and Laser Engineering 40(2): 267-270 (Feb. 2011), 4 pages.
Hall et al., “Sensing of Fluctuating Nanoscale Magnetic Fields Using Nitrogen-Vacancy Centers in Diamond,” Physical Review Letters 103(220802): 1-4 (Nov. 25, 2009), 4 pages.
Hanson et al., “Coherent Dynamics of a Single Spin Interacting with an Adjustable Spin Bath,” Science 320(5874): 352-355 (Apr. 18, 2008), 5 pages.
Hanson et al., “Polarization and Readout of Coupled Single Spins in Diamond,” Physical Review Letters 97(087601): 1-4 (Aug. 23, 2006), 4 pages.
Hanson et al., “Room-temperature manipulation and decoherence of a single spin in diamond,” Physical Review 74(161203): 1-4 (Oct. 26, 2006), 4 pages.
Hanzawa et al., “Zeeman effect on the zero-phonon line of the NV center in synthetic diamond,” Physica B 184(1-4): 137-140 (Feb. 1993), 4 pages.
Heerema, et al. “Graphene nanodevices for DNA sequencing.” Nature nanotechnology 11.2 (Feb. 3, 2016): 127-136.
Hegyi & Yablonovitch, “Molecular imaging by optically detected electron spin resonance of nitrogen-vacancies in nanodiamonds,” Nano Letters 13(3): 1173-1178 (Mar. 2013; first published online Feb. 6, 2013), 6 pages.
Hegyi & Yablonovitch, “Nanodiamond molecular imaging with enhanced contrast and expanded field of view,” Journal of Biomedical Optics 19(1)(011015): 1-8 (Jan. 2014), 9 pages.
Hilser et al., “All-optical control of the spin state in the NV-center in diamond,” Physical Review B 86(125204): 1-8 (Sep. 14, 2012), 8 pages.
Hobbs, “Study of the Environmental and Optical Durability of AR Microstructures in Sapphire, Alon, and Diamond,” SPIE 7302, Window and Dome Technologies and Materials XI, 73020J (Apr. 27, 2009), 14 pages.
Huebener et al., “ODMR of NV centers in nano-diamonds covered with N@C60,” Physica Status Solidi B 245(10): 2013-2017 (Oct. 2008; first published online Sep. 8, 2008), 5 pages.
Huxter et al., “Vibrational and electronic dynamics of nitrogen-vacancy centres in diamond revealed by two-dimensional ultrafast spectroscopy,” Nature Physics 9: 744-749 (Sep. 29, 2013), 6 pages.
International Search Report and Written Opinion from related PCT application PCT/US2017/035315 dated Aug. 24, 2017, 7 pages.
International Search Report and Written Opinion of the International Searching Authority dated Apr. 1, 2016 from related PCT application PCT/US2016/014384, 12 pages.
International Search Report and Written Opinion of the International Searching Authority dated Apr. 11, 2016 from related PCT application PCT/US2016/014376, 12 pages.
International Search Report and Written Opinion of the International Searching Authority dated Apr. 11, 2016 from related PCT application PCT/US2016/014388, 14 pages.
International Search Report and Written Opinion of the International Searching Authority dated Apr. 11, 2016 from related PCT application PCT/US2016/014395, 15 pages.
International Search Report and Written Opinion of the International Searching Authority dated Apr. 4, 2017 from related PCT application PCT/US16/68366, 9 pages.
International Search Report and Written Opinion of the International Searching Authority dated Feb. 15, 2017 from related PCT application PCT/US2016/014390, 20 pages.
International Search Report and Written opinion of the International Searching Authority dated Jul. 12, 2016, from related PCT application PCT/US2016/014287, 14 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jul. 16, 2015, from related PCT application PCT/US2015/24723, 8 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jul. 6, 2015, from related PCT application PCT/US2015/021093, 9 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jul. 8, 2015, from related PCT application PCT/US2015/024265, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 1, 2017, from related PCT application PCT/US17/21811, 9 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 1, 2017, in related PCT application PCT/US17/22279, 20 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 10, 2016 from related PCT application PCT/US2016/014290, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 15, 2017, from related PCT application PCT/US2017/024175, 10 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 2, 2016, from related PCT application PCT/US2016/014386, 14 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 2, 2016, from related PCT application PCT/US2016/014387, 13 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 6, 2016, from related PCT application PCT/US2016/014291, 13 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 9, 2016 from related PCT application PCT/US2016/014333, 16 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 9, 2017, from related patent application PCT/US2017/024181, 13 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 9, 2017, from related PCT application PCT/US2017/024179, 9 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 13, 2017 from related PCT application PCT/US2016/68320, 10 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 24, 2016 from related PCT application PCT/US2016/014336, 17 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 24, 2016 from related PCT application PCT/US2016/014297, 15 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 24, 2016 from related PCT application PCT/US2016/014392, 8 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 24, 2016 from related PCT application PCT/US2016/014403, 10 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 25, 2016, from related PCT application PCT/US2016/014363, 8 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 25, 2016, from related PCT application PCT/US2016/014389, 19 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 27, 2017 from related PCT application PCT/US16/68344, 16 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 28, 2016, from related PCT application PCT/US2016/014380, 9 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 28, 2016, from related PCT application PCT/US2016/014394, 17 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 29, 2016 from related PCT application PCT/US2016/014325, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 29, 2016 from related PCT application PCT/US2016/014330, 8 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 29, 2016, from related PCT application PCT/US2016/014328, 7 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 29, 2016, from related PCT application PCT/US2016/014385, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 30, 2016 from related PCT application PCT/US2016/014298, 14 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 31, 2016 from related PCT application PCT/US2016/014375, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 31, 2016 from related PCT application PCT/US2016/014396, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Mar. 31, 2017 from related PCT application PCT/US2016/066566, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated May 10, 2017 from related PCT application PCT/US17/19411, 8 pages.
International Search Report and Written Opinion of the International Searching Authority dated May 18, 2017, from related PCT application PCT/US2017/021593, 10 pages.
International Search Report and Written Opinion of the International Searching Authority dated May 19, 2017, from related PCT application PCT/US17/18099, 16 pages.
International Search Report and Written Opinion of the International Searching Authority dated May 26, 2016, from related PCT application PCT/US2016/014331, 15 pages.
International Search Report and Written Opinion of the International Searching Authority dated May 3, 2017 from related PCT application PCT/US2017/018701, 8 pages.
International Search Report and Written Opinion of the International Searching Authority dated May 4, 2017 from related PCT application PCT/US2017/018709, 8 pages.
International Search Report and Written Opinion of the International Searching Authority dated May 8, 2017 from related PCT application PCT/US2017/17321, 17 pages.
International Search Report and Written Opinion of the International Searching Authority dated Sep. 13, 2016, from related PCT application PCT/US16/14377, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jul. 14, 2017, from related PCT application PCT/US2017/022118, 13 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jul. 17, 2017, from related PCT application PCT/US2017/024177, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jul. 18, 2017, from related PCT application PCT/US2017/024167, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jul. 18, 2017, from related PCT application PCT/US2017/024173, 13 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jul. 19, 2017, from related PCT application PCT/US2017/024171, 12 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 15, 2017, from related PCT application PCT/US2017/024182, 21 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 22, 2017, in related PCT application PCT/US2017/024180, 10 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 5, 2017, from related PCT application PCT/US2017/024169, 11 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 5, 2017, from related PCT application PCT/US2017/024174, 8 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 5, 2017, in related PCT application PCT/US2017/024168, 7 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 6, 2017, from related PCT application PCT/2017/024165, 9 pages.
International Search Report and Written Opinion of the International Searching Authority dated Jun. 6, 2017, from related PCT application PCT/US2017/024172, 9 pages.
Ivady et al., “Pressure and temperature dependence of the zero-field splitting in the ground state of NV centers in diamond: A first-principles study,” Physical Review B 90(235205): 1-8 (Dec. 2014), 8 pages.
Jarmola et al., “Temperature- and Magnetic-Field-Dependent Longitudinal Spin Relaxation in Nitrogen-Vacancy Ensembles in Diamond,” Physical Review Letters 108 (197601): 1-5 (May 2012), 5 pages.
Jensen et al., “Light narrowing of magnetic resonances in ensembles of nitrogen-vacancy centers in diamond,” Physical Review B 87(014115): 1-10 (Jan. 2013), 10 pages.
Kailath, “Linear Systems,” Prentice Hall, (1979), 6 pages.
Karlsson et al., “Diamond micro-optics: microlenses and antireflection structures surfaces for the infrared spectral region,” Optics Express 11(5): 502-507 (Mar. 10, 2003), 6 pages.
Keyser “Enhancing nanopore sensing with DNA nanotechnology.” Nature nanotechnology 11.2 (Feb. 2016): 106-108.
Khan & Hemmer, “Noise limitation in nano-scale imaging,” Proceedings of SPIE vol. 5842: 302-305, (Dec. 2005), 7 pages.
Kim et al., “Electron spin resonance shift and linewidth broadening of nitrogen-vacancy centers in diamond as a function of electron irradiation dose,” Applied Physics Letters 101(082410): 1-5 (Aug. 2012), 6 pages.
Kim et al., “Jahn-Teller Splitting and Zeeman Effect of Acceptors in Diamond,” Physica B 273-274: 647-627 (Jul. 1999), 4 pages.
Kim et al., “Magnetospectroscopy of acceptors in ‘blue’ diamonds,” Physica B 302-301: 88-100 (Aug. 2001), 13 pages.
Kim et al., “Zeeman effect of electronic Raman lines of accepters in elemental semiconductors: Boron in blue diamond,” Physical Review B 62(12): 8038-8052 (Sep. 2000), 15 pages.
King et al., “Optical polarization of 13C nuclei in diamond through nitrogen vacancy centers,” Physical Review B 81(073201): 1-4 (Feb. 2010), 4 pages.
Kok et al., “Materials Science: Qubits in the pink,” Nature 444(2): 49 (Nov. 2006), 1 page.
Konenko et al., “Formation of antireflective surface structures on diamond films by laser patterning,” Applied Physics A 68:99-102 (Jan. 1999), 4 pages.
Kraus et al., “Magnetic field and temperature sensing with atomic-scale spin defects in silicon carbide,” Scientific Reports 4(5303): 1-8 (Jul. 2014), 8 pages.
Lai et al., “Influence of a static magnetic field on the photoluminescence of an ensemble of nitrogen-vacancy color centers in a diamond single-crystal,” Applied Physics Letters 95, (Sep. 2009), 4 pages.
Lai et al., “Optically detected magnetic resonance of a single Nitrogen-Vacancy electronic spin in diamond nanocrystals,” CLEO/EQEC, (Jun. 14-19, 2009), 1 page.
Laraoui et al., “Nitrogen-vacancy assisted magnetometry of paramagnetic centers in an individual diamond nanocrystal,” Nano Letters 12: 3477-3482 (Jul. 2012), 6 pages.
Lazariev et al., “A nitrogen-vacancy spin based molecular structure microscope using multiplexed projection reconstruction,” Scientific Reports 5(14130): 1-8 (Sep. 2015), 8 pages.
Le Sage et al., “Efficient photon detection from color centers in a diamond optical waveguide,” Phys. Rev. B 85: 121202(R), pp. 121202-1-121202-4, (Mar. 23, 2012), 4 pages.
Lee et al., “Vector magnetometry based on S=3/2 electronic spins,” Physical Review B 92 (115201): 1-7 (Sep. 2015), 7 pages.
Lesik et al., “Preferential orientation of NV defects in CVD diamond films grown on (113)-oriented substrates,” Diamond and Related Materials 56: 47-53 (Jun. 2015), 7 pages.
Levchenko et al., “Inhomogeneous broadening of optically detected magnetic resonance of the ensembles of nitrogen-vacancy centers in diamond by interstitial carbon atoms,” Applied Physics Letters 106, (Mar. 2015; published online Mar. 9, 2015), 6 pages.
Lindsay “The promises and challenges of solid-state sequencing.” Nature nanotechnology 11.2 (Feb. 2016): 109-111.
Liu et al., “Electron spin studies of nitrogen vacancy centers in nanodiamonds,” Acta Physica Sinica 62(16) 164208: 1-5 (Aug. 2013), 5 pages.
Liu et al., “Fiber-integrated diamond-based magnetometer,” Applied Physics Letters 103(143105): 1-4 (Sep. 2013), 5 pages.
MacLaurin et al., “Nanoscale magnetometry through quantum control of nitrogen-vacancy centres in rotationally diffusing nanodiamonds,” New Journal of Physics 15, (Jan. 2013), 16 pages.
MacQuarie et al., “Mechanical spin control of nitrogen-vacancy centers in diamond,” Retrieved from http://www.arxiv.org/pdf/1306.6356.pdf, pp. 1-8, (Jun. 2013), 8 pages.
Macs et al., “Diamond as a magnetic field calibration probe,” Journal of Physics D: Applied Physics 37, (Apr. 2004; published Mar. 17, 2004), 6 pages.
Maletinsky et al., “A robust scanning diamond sensor for nanoscale imaging with single nitrogen-vacancy centres,” Nature Nanotechnology 7: 320-324, (May 2012; published Apr. 15, 2012), 5 pages.
Mamin et al., “Multipulse Double-Quantum Magnetometry with Near-Surface Nitrogen-Vacancy Centers,” Physical Review Letters 13(030803): 1-5 (Jul. 2014), 5 pages.
Mamin et al., “Nanoscale Nuclear Magnetic Resonance with a Nitrogen-Vacancy Spin Sensor,” Science 339, (Feb. 2013), 5 pages.
Manson et al., “GR transitions in diamond: magnetic field measurements,” Journal of Physics C Solid St. Phys 13: L1005-L1009, (Nov. 1980), 6 pages.
Massachusetts Institute of Technology, “Wide-Field Imaging Using Nitrogen Vacancies,” in Patent Application Approval Process, Physics Week: 1-5, (Jan. 20, 2015), 5 pages.
Matlashov, et al. “SQUIDs for magnetic resonance imaging at ultra-low magnetic field.” PIERS online 5.5 (2009): 466-470.
Matlashov, et al. “SQUIDs vs. induction coils for ultra-low field nuclear magnetic resonance: experimental and simulation comparison.” IEEE Transactions on Applied Superconductivity 21.3 (Jan. 1, 2012): 465-468.
Matsuda et al., “Development of a plastic diamond anvil cell for high pressure magneto-photoluminescence in pulsed high magnetic fields,” International Journal of Modern Physics B 18(27-29), (Nov. 2004), 7 pages.
Maze et al., “Nanoscale magnetic sensing using spin qubits in diamond,” Proc. SPIE 7225, Advanced Optical Concepts in Quantum Computing, Memory, and Communication II, 722509 (Feb. 2, 2009) 8 pages.
Maze et al., “Nanoscale magnetic sensing with an individual electronic spin in diamond,” Nature Physics 455: 644-647 (Oct. 2, 2008), 5 pages.
Meijer et al., “Generation of single color centers by focused nitrogen implantation,” Applied Physics Letters 87(261909): 1-3 (Dec. 2005), 4 pages.
Michaelovich et al., “Polarization Dependencies of the Nitrogen-Vacancy Center.” Undergraduate Project Report, Ben-Gurion University, Aug. 2015, pp. 1-9.
Millot et al., “High-field Zeeman and Paschen-Back effects at high pressure in oriented ruby,” Physical Review B 78 (155125): 1-7 (Oct. 2008), 7 pages.
Moessle, et al. “SQUID-detected magnetic resonance imaging in microtesla fields.” Annu. Rev. Biomed. Eng. 9 (May 23, 2008): 389-413.
Moriyama et al., “Importance of electron-electron interactions and Zeeman splitting in single-wall carbon nanotube quantum dots,” Physica E 26: 473-476 (Feb. 2005), 4 pages.
Mrozek et al., “Circularly polarized microwaves for magnetic resonance study in the GHz range: Application to nitrogen-vacancy in diamonds,” Applied Physics Letters, pp. 1-4 (Jul. 2015), 4 pages.
Nagl et al., “Improving surface and defect center chemistry of fluorescent nanodiamonds for imaging purposes—a review,” Analytical and Bioanalaytical Chemistry 407: 7521-7536 (Oct. 2015; published online Jul. 29, 2015), 16 pages.
Neumann et al., “Excited-state spectroscopy of single NV defects in diamond using optically detected magnetic resonance,” New Journal of Physics 11(013017): 1-10, (Jan. 2009), 11 pages.
Nizovtsev & Kilin, “Optically Detected Magnetic Resonance Spectra of the 14NV—13C Spin Systems in Diamond: Analytical Theory and Experiment,” Doklady of the National Academy of Sciences of Belarus, (2013), 27 pages with English machine translation.
Nizovtsev et al., “Modeling fluorescence of single nitrogen-vacancy defect centers in diamond,” Physica B—Condensed Matter, 608-611 (Dec. 2001), 4 pages.
Nizovtsev et al., “Theoretical study of hyperfine interactions and optically detected magnetic resonance spectra by simulation of the C-291(NV)H-(172) diamond cluster hosting nitrogen-vacancy center,” New Journal of Physics 16(083014): 1-21 (Aug. 2014), 22 pages.
Nobauer et al., “Smooth optimal quantum control for robust solid state spin magnetometry,” Retrieved from http://www.arxiv.org/abs/1412.5051, pp. 1-12, (Dec. 2014), 12 pages.
Nowodzinski et al., “Nitrogen-Vacancy centers in diamond for current imaging at the redistributive layer level of Integrated Circuits,” Microelectronics Reliability 55: 1549-1553 (Aug. 2015), 5 pages.
Nusran et al., “Optimizing phase-estimation algorithms for diamond spin magnetometry,” Physical Review B 90(024422): 1-12 (Jul. 2014), 12 pages.
Ohashi et al., “Negatively Charged Nitrogen-Vacancy Centers in a 5 nm Thin 12C Diamond Film,” Nano Letters 13: 4733-4738 (Oct. 2013), 6 pages.
Pelliccione, et al., Two-dimensional nanoscale imaging of gadolinium spins via scanning probe relaxometry with a single spin in diamond, Phys. Rev. Applied 2.5, (Sep. 8, 2014): 054014 pp. 1-17.
Plakhotnik et al., “Super-Paramagnetic Particles Chemically Bound to Luminescent Diamond : Single Nanocrystals Probed with Optically Detected Magnetic Resonance,” Journal of Physical Chemistry C 119: 20119-20124 (Aug. 2015), 6 pages.
Polatomic. “AN/ASQ-233A Digital Magnetic Anomaly Detective Set.” Retrieved May 9, 2016, from http://polatomic.com/images/DMAD_Data_Sheet_09-2009.pdf (2009), 1 page.
Poole, “What is GMSK Modulation—Gaussian Minimum Shift Keying.” Radio-Electronics, retrieved from https://web.archive.org/web/20150403045840/http://www.radio-electronics.com/info/rf-technology-design/pm-phase-modulation/what-is-gmsk-gaussian-minimum-shift-keyingtutorial.php (Apr. 3, 2015), 4 pages.
Qiu et al., “Low-field NMR Measurement Procedure when SQUID Detection is Used,” IEEE/CSC & ESAS European Superconductivity News Forum, No. 5, Jul. 2008.
Qiu, et al. “SQUID-detected NMR in Earth's magnetic field.” Journal of Physics: Conference Series. vol. 97. No. 1. IOP Publishing, Mar. 2008, pp. 1-7.
Rabeau et al., “Implantation of labelled single nitrogen vacancy centers in diamond using 15N,” Applied Physics Letters 88, (Jan. 2006), 4 pages.
Ramsey, et al., “Phase Shifts in the Molecular Beam Method of Separated Oscillating Fields”, Physical Review, vol. 84, No. 3, Nov. 1, 1951, pp. 506-507.
Ranjbar et al., “Many-electron states of nitrogen-vacancy centers in diamond and spin density calculations,” Physical Review B 84(165212): 1-6 (Oct. 2011), 6 pages.
Reynhardt, “Spin-lattice relaxation of spin-1/2 nuclei in solids containing diluted paramagnetic impurity centers. I. Zeeman polarization of nuclear spin system,” Concepts in Magnetic Resonance Part A, pp. 20-35, (Sep. 2003), 16 pages.
Rogers et al., “Singlet levels of the NV(−) centre in diamond,” New Journal of Physics 17, (Jan. 2015), 13 pages.
Rondin et al., “Magnetometry with nitrogen-vacancy defects in diamond,” Reports on Progress in Physics 77(056503) 1-26 (May 2014), 27 pages.
Rondin et al., “Magnetometry with nitrogen-vacancy defects in diamond.” May 22, 2014 (May 22, 2014), pp. 1 [online] http://arxiv.org/pdf/1311.5214.pdf, 29 pages.
Rondin et al., “Nanoscale magnetic field mapping with a single spin scanning probe magnetometer,” Applied Physics Letters 100, (Apr. 2012), 5 pages.
Sarkar et al., “Magnetic properties of graphite oxide and reduced graphene oxide,” Physica E 64: 78-82 (Nov. 2014), 5 pages.
Scheuer et al., “Accelerated 2D magnetic resonance spectroscopy of single spins using matrix completion,” Scientific Reports 5(17728): 1-8 (Dec. 2015), 8 pages.
Schirhagl et al., “Nitrogen-vacancy centers in diamond: Nanoscale sensors for physics and biology,” Annual Review of Physical Chemistry 65: 83-105 (Jan. 2014), 26 pages.
Schoenfeld & Harneit, “Real time magnetic field sensing and imaging using a single spin in diamond,” Physical Review Letters 106(030802): 1-4 (Jan. 2011), 4 pages.
Sedov et al., “Si-doped nano- and microcrystalline diamond films with controlled bright photoluminescence of silicon-vacancy color centers,” Diamond and Related Materials 56: 23-28 (Jun. 2015; available online Apr. 18, 2015), 6 pages.
Shames et al., “Magnetic resonance tracking of fluorescent nanodiamond fabrication,” Journal of Physics D: Applied Physics 48(155302): 1-13 (Apr. 2015; published Mar. 20, 2015), 14 pages.
Shao et al., “Diamond Color Center Based FM Microwave Demodulator,” in Conference on Lasers and Electro-Optics, OSA Technical Digest (online) (Optical Society of America), paper JTh2A.136, (Jun. 5-10, 2016), 2 pages.
Sheinker et al., “Localization in 3-D Using Beacons of Low Frequency Magnetic Field.” IEEE Transactions on Instrumentation and Measurement 62(12): 3194-3201 (Dec. 2013), 8 pages.
Simanovskaia et al., “Sidebands in optically detected magnetic resonance signals of nitrogen vacancy centers in diamond,” Physical Review B 87(224106): 1-11 (Jun. 2013), 11 pages.
Sotoma et al., “Effective production of fluorescent nanodiamonds containing negatively-charged nitrogen-vacancy centers by ion irradiation,” Diamond and Related Materials 49: 33-38 (Oct. 2014), 6 pages.
Soykal et al., “Quantum metrology with a single spin-3/2 defect in silicon carbide,” Mesoscale and Nanoscale Physics (May 24, 2016), retrieved from https://arxiv.org/abs/1605.07628 (Sep. 22, 2016), 9 pages.
Steiner et al., “Universal enhancement of the optical readout fidelity of single electron spins at nitrogen-vacancy centers in diamond,” Physical Review B 81(035205): 1-6 (Jan. 2010), 6 pages.
Steinert et al., “High-sensitivity magnetic imaging using an array of spins in diamond,” Rev. Sci. Inst. 81(043705): 1-5 (Apr. 23, 2010), 5 pages.
Steinert et al., “Magnetic spin imaging under ambient conditions with sub-cellular resolution.” Nature Comms 4:1607 (Mar. 19, 2013).
Stepanov et al., “High-frequency and high-field optically detected magnetic resonance of nitrogen-vacancy centers in diamond,” Applied Physics Letters 106, (Feb. 2015), 5 pages.
Sternschulte et al., “Uniaxial stress and Zeeman splitting of the 1.681 eV optical center in a homoepitaxial CVD diamond film,” Diamond and Related Materials 4: 1189-1192 (Sep. 1995), 4 pages.
Storteboom et al., “Lifetime investigation of single nitrogen vacancy centres in nanodiamonds,” Optics Express 23(9): 11327-11333 (May 4, 2015; published Apr. 22, 2015), 7 pages.
Sushkov, et al. “All-optical sensing of a single-molecule electron spin.” Nano letters 14.11 (Nov. 7, 2013): 6443-6448.
Tahara et al., “Quantifying selective alignment of ensemble nitrogen-vacancy centers in (111) diamond,” Applied Physics Letters 107:193110 (Nov. 2015; published online Nov. 13, 2015), 5 pages.
Taylor et al., “High-sensitivity diamond magnetometer with nanoscale resolution,” Nature Physics 4: 810-816 (Oct. 2008), 7 pages.
Teale, “Magnetometry with Ensembles of Nitrogen Vacancy Centers in Bulk Diamond,” Master's Thesis, Massachusetts Institute of Technology Department of Electrical Engineering and Computer Science (Sep. 2015), 57 pages.
Terblanche et al., “13C spin-lattice relaxation in natural diamond: Zeeman relaxation at 4.7 T and 300 K due to fixed paramagnetic nitrogen defects,” Solid State Nuclear Magnetic Resonance 20: 1-22 (Aug. 2001), 22 pages.
Terblanche et al., “13C spin-lattice relaxation in natural diamond: Zeeman relaxation in fields of 500 to 5000 G at 300 K due to fixed paramagnetic nitrogen defects,” Solid State Nuclear Magnetic Resonance 19: 107-129 (May 2001), 23 pages.
Tetienne et al., “Magnetic-field-dependent photodynamics of single NV defects in diamond: an application to qualitative all-optical magnetic imaging,” New Journal of Physics 14(103033): 1-5 (Oct. 2012), 16 pages.
Tetienne, et al. “Spin relaxometry of single nitrogen-vacancy defects in diamond nanocrystals for magnetic noise sensing.” Physical Review B 87.23 (Apr. 3, 2013): 235436-1-235436-5.
Tong et al., “A hybrid-system approach for W state and cluster state generation,” Optics Communication 310: 166-172, (Jan. 2014; available online Aug. 12, 2013), 7 pages.
Uhlen et al., “New diamond nanofabrication process for hard x-ray zone plates,” J. of Vacuum Science & Tech. B 29(6) (06FG03): 1-4 (Nov./Dec. 2011), 4 pages.
U.S. Notice of Allowance dated Apr. 20, 2016, from related U.S. Appl. No. 15/003,718, 9 pages.
U.S. Notice of Allowance dated Aug. 11, 2017 from related U.S. Appl. No. 15/003,558, 5 pages.
U.S. Notice of Allowance dated Aug. 17, 2016, from related U.S. Appl. No. 15/003,718, 8 pages.
U.S. Notice of Allowance dated Dec. 13, 2016, from related U.S. Appl. No. 14/680,877, 8 pages.
U.S. Notice of Allowance dated Dec. 22, 2016, from related U.S. Appl. No. 14/659,498, 10 pages.
U.S. Notice of Allowance dated Feb. 14, 2017, from related U.S. Appl. No. 15/003,677, 8 pages.
U.S. Notice of Allowance dated Jul. 18, 2017 from related U.S. Appl. No. 15/003,634, 6 pages.
U.S. Notice of Allowance dated Jul. 24, 2017 from related U.S. Appl. No. 15/003,088, 12 pages.
U.S. Notice of Allowance dated Jun. 20, 2017, from related U.S. Appl. No. 15/204,675, 9 pages.
U.S. Notice of Allowance dated Jun. 28, 2017 from related U.S. Appl. No. 15/003,256, 10 pages.
U.S. Notice of Allowance dated Jun. 8, 2017, from related U.S. Appl. No. 15/351,862, 7 pages.
U.S. Notice of Allowance dated Mar. 15, 2017, from related U.S. Appl. No. 15/351,862, 6 pages.
U.S. Notice of Allowance dated Mar. 29, 2016, from related U.S. Appl. No. 15/003,590, 11 pages.
U.S. Notice of Allowance dated May 26, 2017 from related U.S. Appl. No. 15/218,821, 7 pages.
U.S. Notice of Allowance dated Sep. 1, 2017, from related U.S. Appl. No. 14/676,740, 7 pages.
U.S. Notice of Allowance dated Sep. 14, 2017, from related U.S. Appl. No. 15/476,636, 10 pages.
U.S. Notice of Allowance dated Sep. 18, 2017, from related U.S. Appl. No. 15/003,206, 11 pages.
U.S. Notice of Allowance dated Sep. 26, 2017, from related U.S. Appl. No. 15/003,281, 7 pages.
U.S. Notice of Allowance dated Sep. 8, 2016, from related U.S. Appl. No. 15/003,298, 10 pages.
U.S. Office Action dated Apr. 17, 2017, from related U.S. Appl. No. 15/003,558, 12 pages.
U.S. Office Action dated Aug. 15, 2017 from related U.S. Appl. No. 15/003,281, 12 pages.
U.S. Office Action dated Aug. 24, 2016 from related U.S. Appl. No. 14/676,740, 19 pages.
U.S. Office Action dated Feb. 10, 2017, from related U.S. Appl. No. 14/676,740, 20 pages.
U.S. Office Action dated Feb. 10, 2017, from related U.S. Appl. No. 15/003,088, 11 pages.
U.S. Office Action dated Feb. 16, 2017, from related U.S. Appl. No. 15/204,675, 7 pages.
U.S. Office Action dated Jul. 27, 2017 from related U.S. Appl. No. 15/003,577, 15 pages.
U.S. Office Action dated Jul. 29, 2016 from related U.S. Appl. No. 14/680,877, 8 pages.
U.S. Office Action dated Jun. 1, 2017, from related U.S. Appl. No. 15/003,797, 29 pages.
U.S. Office Action dated Jun. 1, 2017, from related U.S. Appl. No. 15/179,957, 29 pages.
U.S. Office Action dated Jun. 12, 2017, from related U.S. Appl. No. 15/003,256, 9 pages.
U.S. Office Action dated Jun. 12, 2017, from related U.S. Appl. No. 15/003,336, 14 pages.
U.S. Office Action dated Jun. 16, 2017, from related U.S. Appl. No. 15/003,678, 15 pages.
U.S. Office Action dated Jun. 2, 2017, from related U.S. Appl. No. 15/476,636, 10 pages.
U.S. Office Action dated Mar. 1, 2017, from related U.S. Appl. No. 15/003,634, 7 pages.
U.S. Office Action dated Mar. 16, 2017, from related U.S. Appl. No. 15/218,821, 7 pages.
U.S. Office Action dated May 13, 2016, from related U.S. Appl. No. 14/676,740, 15 pages.
U.S. Office Action dated May 22, 2017, from related U.S. Appl. No. 15/003,206, 12 pages.
U.S. Office Action dated May 6, 2016, from related U.S. Appl. No. 14/659,498.
U.S. Office Action dated Nov. 2, 2016, from related U.S. Appl. No. 15/003,256, 19 pages.
U.S. Office Action dated Nov. 3, 2016, from related U.S. Appl. No. 15/204,675, 9 pages.
U.S. Office Action dated Oct. 14, 2016 from related U.S. Appl. No. 15/003,677, 13 pages.
U.S. Office Action dated Oct. 19, 2016, from related U.S. Appl. No. 15/218,821, 6 pages.
U.S. Office Action dated Sep. 27, 2017, from related U.S. Appl. No. 15/003,176, 8 pages.
U.S. Office Action dated Sep. 8, 2017, from related U.S. Appl. No. 15/003,292, 8 pages.
Vershovskii & Dmitriev, “Combined excitation of an optically detected magnetic resonance in nitrogen-vacancy centers in diamond for precision measurement of the components of a magnetic field vector,” Technical Physics Letters 41(11): 1026-1029 (Nov. 2015), 4 pages.
Vershovskii & Dmitriev, “Micro-scale three-component quantum magnetometer based on nitrogen-vacancy color centers in diamond crystal,” Technical Physics Letters 41(4): 393-396 (Apr. 2015), 4 pages.
Wahlstrom et al., “Modeling Magnetic Fields Using Gaussian Processes,” 2013 IEEE International Conference on Acoustics, Speech, and Signal Processing, pp. 3522-3526 (May 26-31, 2013), 5 pages.
Wang et al., “Optimizing ultrasensitive single electron magnetometer based on nitrogen-vacancy center in diamond,” Chinese Science Bulletin, 58(24): 2920-2923, (Aug. 2013), 4 pages.
Webber et al., “Ab initio thermodynamics calculation of the relative concentration of NV- and NV0 defects in diamond,” Physical Review B 85,(014102): 1-7 (Jan. 2012), 7 pages.
Wells, et al. “Assessing graphene nanopores for sequencing DNA.” Nano letters 12.8 (Jul. 10, 2012): 4117-4123.
Widmann et al., “Coherent control of single spins in silicon carbide at room temperature,” Nature Materials, 14: 164-168 (2015) (available online Dec. 1, 2014), 5 pages.
Wolf et al., “Subpicotesla Diamond Magnetometry,” Physical Review X 5(041001): 1-10 (Oct. 2015), 10 pages.
Wolfe et al., “Off-resonant manipulation of spins in diamond via precessing magnetization of a proximal ferromagnet,” Physical Review B 89(180406): 1-5 (May 2014), 5 pages.
Wroble, “Performance Analysis of Magnetic Indoor Local Positioning System.” Western Michigan University Master's Theses, Paper 609 (Jun. 2015), 42 pages.
Wysocki et al., “Modified Walsh-Hadamard sequences for DS CDMA wireless systems.” Int. J. Adaptive Control and Signal Processing 16(8): 589-602 (Oct. 2002; first published online Sep. 23, 2002), 25 pages.
Xue & Liu, “Producing GHZ state of nitrogen-vacancy centers in cavity QED,” Journal of Modern Optics 60(6-7), (Mar. 2013), 8 pages.
Yang & Gu, “Novel calibration techniques for high pulsed-magnetic fields using luminescence caused by photo,” (with English machine translation), Journal of Huazhong University of Science and Technology, (Jun. 2007), 11 pages.
Yavkin et al., “Defects in Nanodiamonds: Application of High-Frequency cw and Pulse EPR, ODMR,” Applied Magnetic Resonance, 45: 1035-1049 (Oct. 2014; published online Sep. 10, 2014), 15 pages.
Yu et al., “Bright fluorescent nanodiamonds: no photobleaching and low cytotoxicity,” J. Am. Chem. Soc., 127: 17604-17605 (Nov. 25, 2005), 2 pages.
Zhang et al., “Laser-polarization-dependent and magnetically controlled optical bistability in diamond nitrogen-vacancy centers,” Physics Letters A 377: 2621-2627 (Nov. 2013), 7 pages.
Zhang et al., “Laser-polarization-dependent spontaneous emission of the zero phonon line from single nitrogen-vacancy center in diamond,” Chinese Physics B 24(3), (Apr. 2014), 13 pages.
Zhang et al., “Scalable quantum information transfer between nitrogen-vacancy-center ensembles,” Annals of Physics, 355: 170-181 (Apr. 2015; available online Feb. 14, 2013), 12 pages.
Zhao et al., “Atomic-scale magnetometry of distant nuclear spin clusters via nitrogen-vacancy spin in diamond,” Nature Nanotechnology, 5: 242-246 (Apr. 2011), 5 pages.
European Extended Search Report for Appl. Ser. No. 16743879.5 dated Sep. 11, 2018, 11 pages.
European Extended Search Report for Appl. Ser. No. 16800410.9 dated Oct. 12, 2018, 11 pages.
Fenglian Niu, “Crack Detection of Power Line Based on Metal Magnetic Memory Non-destructive”, Telkomnika Indonesian Journal of Electrical Engineering, vol. 12, No. 11, Nov. 1, 2014, pp. 7764-7771.
U.S. Final Office Action for U.S. Appl. No. 15/380,691 dated Sep. 21, 2018, 12 pages.
U.S. Final Office Action for U.S. Appl. No. 15/479,256 dated Sep. 10, 2018, 20 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/443,422 dated Oct. 2, 2018, 16 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/446,373 dated Oct. 1, 2018, 13 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/454,162 dated Sep. 10, 2018, 13 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/468,282 dated Oct. 10, 2018, 12 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/372,201 dated Oct. 15, 2018, 12 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/468,274 dated Oct. 26, 2018, 11 pages.
U.S. Notice of Allowance for U.S. Appl. No. 14/866,730 dated Aug. 15, 2018, 9 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/468,289 dated Oct. 17, 2018, 12 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/003,704 dated Nov. 2, 2018, 19 pages.
U.S. Office Action for U.S. Appl. No. 15/468,397 dated Sep. 13, 2018, 7 pages.
Bui et al., “Noninvasive Fault Monitoring of Electrical Machines by Solving the Steady-State Magnetic Inverse Problem,” in IEEE Transactions on Magnetics, vol. 44, No. 6, pp. 1050-1053, Jun. 24, 2008.
Chadebec et al., “Rotor fault detection of electrical machines by low frequency magnetic stray field analysis,” 2005 5th IEEE International Symposium on Diagnostics for Electric Machines, Power Electronics and Drives, Vienna, 2005, submitted Mar. 22, 2006, pp. 1-6.
Froidurot et al., “Magnetic discretion of naval propulsion machines,” in IEEE Transactions on Magnetics, vol. 38, No. 2, pp. 1185-1188, Mar. 2002.
IEEE Std 802.11 TM-2012 Wireless LAN Medium Access Control (MAC) and Physical Layer (PHY) Specifications, 1 page.
Kwon et al., “Analysis of the far field of permanent-magnet motors and effects of geometric asymmetries and unbalance in magnet design,” in IEEE Transactions on Magnetics, vol. 40, No. 2, pp. 435-442, Mar. 2004.
Maertz et al., “Vector magnetic field microscopy using nitrogen vacancy centers in diamond”, Applied Physics Letters 96, No. 9, Mar. 1, 2010, pp. 092504-1-092504-3.
U.S. Notice of Allowance dated Feb. 2, 2018, from related U.S. Appl. No. 15/003,292, 8 pages.
U.S. Notice of Allowance dated Feb. 21, 2018, from related U.S. Appl. No. 15/003,176, 9 pages.
U.S. Office Action dated Feb. 1, 2018, from related U.S. Appl. No. 15/003,577, 16 pages.
U.S. Office Action dated Feb. 5, 2018, from related U.S. Appl. No. 15/450,504, 12 pages.
U.S. Office Action dated Jan. 25, 2018, from related U.S. Appl. No. 15/672,953, 28 pages.
U.S. Office Action dated Jan. 26, 2018, from related U.S. Appl. No. 15/003,678, 14 pages.
U.S. Office Action dated Mar. 27, 2018, from related U.S. Appl. No. 15/468,386, 21 pages.
U.S. Office Action dated Mar. 28, 2018, from related U.S. Appl. No. 15/003,177, 12 pages.
U.S. Office Action dated Mar. 5, 2018, from related U.S. Appl. No. 14/866,730, 14 pages.
U.S. Office Action dated Mar. 8, 2018, from related U.S. Appl. No. 15/380,691, 12 pages.
U.S. Office Action dated Mar. 8, 2018, from related U.S. Appl. No. 15/479,256, 30 pages.
Wegerich, “Similarity based modeling of time synchronous averaged vibration signals for machinery health monitoring,” 2004 IEEE Aerospace Conference Proceedings (IEEE Cat. No. 04TH8720), 2004, pp. 3654-3662 vol. 6.
Wikipedia, “Continuous phase modulation”, downloaded from https://web.archive.org/web/20151017015236/https://en.wikipedia.org/wiki/Continuous_phase_modulation on May 10, 2017, 3 pages.
Wikipedia, “Minimum-shift keying”, downloaded from https://web.archive.org/web/20151017175828/https://en.wikipedia.org/wiki/Minimum-shift_keying on May 10, 2017, 2 pages.
European Extended Search Report for Appl. Ser. No. 16740794.9 dated Nov. 12, 2018, 12 pages.
Halbach et al., “Design of Permanent Multipole Magnets with Oriented Rare Earth Cobalt Material”, Nuclear Instruments and Methods, North Holland Publishing Co., Amsterdam, NL., vol. 169, Jan. 1, 1980, pp. 1-5, XP001032085, DOI: 10.1016/0029-554X(80) 90094-4.
Hodges et al., “Time-keeping with electron spin states in diamond”, Dept. of Electrical Engineering and Dept. of Applied Physics and Applied Mathematics, Columbia University, New York, New York 10027, Aug. 30, 2011, 13 pages.
Hodges et al., Appendix, “Time-keeping with electron spin states in diamond”, Dept. of Electrical Engineering and Dept. of Applied Physics and Applied Mathematics, Columbia University, New York, New York 10027, Aug. 27, 2012, 46 pages.
International Search Report and Written Opinion for PCT Appl. Ser. No. PCT/US2018/041527 dated Feb. 4, 2019, 22 pages.
US Ex Parte Quayle Action for U.S. Appl. No. 15/468,641 dated Nov. 28, 2018, 11 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/003,177 dated Jan. 14, 2019, 15 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/003,670 dated Nov. 27, 2018, 14 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/382,045 dated Dec. 31, 2018, 16 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/400,794 dated Jan. 10, 2019, 6 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/468,356 dated Jan. 2, 2019, 10 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/003,670 dated Feb. 1, 2019, 7 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/350,303 dated Dec. 26, 2018, 10 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/450,504 dated Dec. 13, 2018, 7 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/454,162 dated Jan. 17, 2019, 8 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/468,397 dated Dec. 12, 2018, 5 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/468,641 dated Feb. 7, 2019, 10 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/479,256 dated Feb. 4, 2019, 7 pages.
International Search Report and Written Opinion for PCT Appl. Ser. No. PCT/US2018/041411 dated Feb. 8, 2019, 13 pages.
Schonfeld, “Optical readout of single spins for quantum computing and magnetic sensing”, Dissertation, Fachbereich Physlk der Freien Universitat Berlin, May 1, 2011, 21 Pages (relevant pages only), XP055143403. Retrieved from the Internet: URL: http://www.diss.fu-berlin.de/diss/servlets/MCRFIleNodeServleUFU DISS_derivate _000000012199/Dissertation_Slmon-choenfela PublIcVersion-2.pdfJsessionid-89A943688E59.
U.S. Final Office Action for U.S. Appl. No. 15/003,396 dated Mar. 22, 2019, 13 pages.
U.S. Final Office Action for U.S. Appl. No. 15/382,045 dated Apr. 26, 2019, 16 pages.
U.S. Final Office Action for U.S. Appl. No. 15/443,422 dated Mar. 7, 2019, 17 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/003,193 dated Apr. 11, 2019, 7 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/003,309 dated Feb. 13, 2019, 16 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/003,617 dated Feb. 26, 2019, 10 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/372,201 dated Apr. 2, 2019, 10 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/419,832 dated Feb. 8, 2019, 12 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/440,194 dated Feb. 15, 2019, 21 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/446,373 dated Apr. 19, 2019, 8 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/468,314 dated Mar. 28, 2019, 17 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/468,410 dated Apr. 11, 2019, 15 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/468,559 dated Apr. 11, 2019, 12 pages.
U.S. Non-Final Office Action for U.S. Appl. No. 15/469,374 dated Feb. 28, 2019, 14 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/003,617 dated Apr. 30, 2019, 9 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/207,457 dated Mar. 6, 2019, 16 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/376,244 dated Feb. 21, 2019, 7 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/380,419 dated Feb. 26, 2019, 5 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/400,794 dated Apr. 25, 2019, 5 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/437,038 dated Mar. 21, 2019, 13 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/437,222 dated Mar. 25, 2019, 11 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/468,282 dated Feb. 19, 2019, 8 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/468,356 dated Apr. 22, 2019, 8 pages.
U.S. Notice of Allowance for U.S. Appl. No. 15/468,582 dated Mar. 21, 2019, 13 pages.
Related Publications (1)
Number Date Country
20180275211 A1 Sep 2018 US