The present disclosure relates to a diamond magneto-optical sensor. The present application claims priority under Japanese Patent Application Nc. 2021/059798 filed on Mar. 31, 2021, which is incorporated herein by reference.
A magneto-optical sensor using the center of NV (hereinafter referred to as a NV center) in diamond is known. When nitrogen at a substitution position of carbon in diamond and an NV center having a vacancy next to the nitrogen are negatively charged, the ground state becomes a triplet state (that is, a spin S=1). The NV center excited at a wavelength 532 nm (that is, green light) emits fluorescence at a wavelength 637 nm (that is, red light). The radiant intensity of fluorescence changes according to a spin state. The spin state is changed by magnetic resonance occurring due to a magnetic field applied to the NV center and microwaves or radio waves, which is applicable to a diamond magneto-optical sensor.
A diamond magneto-optical sensor includes a diamond substrate containing an NV center, an optical system that transmits excitation light from a light source and emits the light to the NV center, an optical system that condenses fluorescence from the NV center and transmits the fluorescence to a photodetector, and a waveguide that transmits microwaves from a power supply and emits the microwaves to the NV center.
For example, NPL 1 discloses a configuration for emitting microwaves with a diamond sensor placed on a coplanar waveguide. A diamond substrate is shaped like a rectangular solid. Excitation light is laterally emitted to the diamond substrate, and fluorescence is condensed from a position above the diamond substrate.
A diamond magneto-optical sensor according to an aspect of the present disclosure includes: a diamond including a color center with an electronic spin, and a reflecting surface that reflects excitation light propagated through an optical system into the diamond, wherein the reflecting surface reflects light radiated from the color center excited by the excitation light and condenses the light in the direction of the optical system.
A diamond magneto-optical sensor according to another aspect of the present disclosure includes: a diamond including a color center with an electronic spin, a small portion that allows excitation light propagated through an optical system to be emitted into the diamond, and a reflecting surface that reflects radiated light radiated from the color center excited by the excitation light incident from the small portion and condenses the light in the direction of a light-receiving optical system that guides the light to a light-receiving element, wherein the reflecting surface has a larger area than the small portion and guides light radiated from the same position in different directions, to the light-receiving optical system through a plurality of optical paths.
An optical system for transmitting excitation light from a light source and emits the light to an NV center initializes the spin state of the NV center and emits excitation light in order to read subsequent changes. In order to obtain high responsivity and sensitivity as a magneto-optical sensor, excitation light needs to be emitted to the NV center with maximum uniformity and intensity over the widest range.
An optical system for condensing fluorescence from the NV center and transmitting the fluorescence to a photodetector condenses fluorescence that changes due to the spin state of the NV center. In order to obtain high responsivity and sensitivity as a magneto-optical sensor, fluorescence from the NV center needs to be condensed with maximum efficiency over the widest range.
In other words, it is preferable to improve the condensing efficiency of fluorescence radiated from the NV center of diamond, the absorption efficiency of excitation light for exciting the NV center, and the radiation power density of excitation light. The problems will be specifically described below.
ϕc denotes the diameter of the core of an optical fiber for transmitting fluorescence, Nc denotes a numerical aperture, n denotes the refractive index of diamond, ϕd denotes the diameter of an area where fluorescence can be condensed from the NV center in diamond, dd denotes a depth where fluorescence can be condensed, and Nd denotes a numerical aperture that allows condensing of fluorescence. In this case, the law of Lagrangian invariant and refraction on a diamond surface restrict the product of ϕd and Nd as follows:
ϕd×Nd<ϕc×Nc/n (Formula 1)
Moreover, dd is determined as follows:
dd=ϕd/Nd (Expression 2)
For example, if diamond is disposed in contact with the core on one end of an optical fiber, ϕc=ϕd can be suggested and Formula 3 is introduced from Formula 1.
Nd<Nc/n (Formula 3)
Numerical aperture Nc of a commercial optical fiber ranges from about 0.07 to about 0.5. Even if an optical fiber with a large numerical aperture (e.g., Nc=0.5) is selected for use, refractive index n of diamond is about 2.5 and thus numerical aperture Nd that allows condensing is determined as Nd<0.2 from Formula 3. Thus, on the assumption that fluorescence from the NV center is randomly radiated substantially over the sky, a condensing rate η of fluorescence that reaches the end face of the optical fiber and is transmitted through the optical fiber is determined as expressed in Expression 4 with respect to a solid angle 4πsr (steradian) over the sky.
η≈(0.2×0.2×π)/(4×π)=0.01 (Expression 4)
Hence, the maximum efficiency remains at 1%.
For example, light may be condensed with an objective lens disposed between diamond and the core of the end face of the optical fiber. In this case, if the objective lens has a numerical aperture Nt, the efficiency is maximized when an optical system has a magnification of Nt/Nc. Also in this case, however, ϕd=Nc×ϕc/Nt is determined and numerical aperture Nd is limited as expressed in Formula 5.
Nd<NT/n (Formula 5)
Since maximum numerical aperture Nt of the objective lens remains at about 1, even a combination with an optical fiber with a large numerical aperture Nc (e.g., Nc=0.5) determines refractive index n of diamond at about 2.5, so that Nd<0.4 is obtained from Formula 5. Thus, condensing rate n of fluorescence that reaches the end face of the optical fiber and is transmitted through the optical fiber is determined as expressed in Expression 6.
η=(0.4×0.4×π)/(4×π)=0.04 (Expression 6)
Hence, the maximum efficiency remains at 4%.
As described above, if the optical fiber is used for transmitting fluorescence from the NV center to the photodetector for the convenience of measurement of high-voltage power equipment, the condensing rate of fluorescence from the NV center remains at about several percents at the most.
As a theoretical formula of sensitivity δB (that is, the resolution of a detected magnetic field B) of the diamond magneto-optical sensor, Formula 7 expressed below is known.
In Formula 7, γ is a gyromagnetic ratio (that is, a constant) that is a value close to the gyromagnetic ratio of an electron (1.76×1011rad/s/T). η is the detection efficiency of fluorescence, that is, condensing efficiency that remains at several percents as described above. C is a spin detection contrast ratio (that is, a decreasing rate of red light brightness), which will be described later. N is the number of NV centers that are irradiated with excitation light and carry negative electrical charge in an area where fluorescence is condensed. T2 is a transverse relaxation time of an electronic spin. According to the theoretical formula of sensitivity (Formula 7), light quantum noise determines the limit of measurement sensitivity in the magneto-optical sensor. Thus, high condensing efficiency η of fluorescence is preferable but the condensing efficiency of fluorescence is several percents, which is not sufficiently high.
In order to initialize the spin state of the NV center and read subsequent changes, excitation light at a wavelength of 532 nm is emitted. For the light source of excitation light, a green-light semiconductor laser or a YAG second-harmonic-wave solid state laser is easy to use. Diamond is classified depending upon the presence or absence of impurity or the kind of impurity. Type Ib containing a nitrogen atom as impurity (that is, including an NV center) looks relatively yellow with low transmittance among kinds of diamond.
For the NV center formed in the type-Ib diamond substrate, the relationship between a spin detection contrast ratio (that is, a decreasing rate of red light brightness) and the power density of excitation light was experimentally evaluated. The result is shown in
For the NV center formed in the type-Ib diamond substrate, the relationship between a response speed relative to a frequency change of microwaves (specifically, a time constant) and the power density of excitation light was experimentally evaluated. Consequently, it is understood that the power density of excitation light to be emitted needs to be increased to obtain a high response speed as a magneto-optical sensor.
Thus, an object of the present disclosure is to provide a diamond magneto-optical sensor that obtains high condensing efficiency of fluorescence and high absorption efficiency and power density of excitation light.
The present disclosure can provide a diamond magneto-optical sensor that obtains high condensing efficiency of fluorescence and high absorption efficiency and power density of excitation light.
The contents of an embodiment of the present disclosure will be described in list form. At least parts of the embodiment below may be combined as required.
(1) A diamond magneto-optical sensor according to a first aspect of the present disclosure includes: a diamond including a color center with an electronic spin, and a reflecting surface that reflects excitation light propagated through an optical system into the diamond, wherein the reflecting surface reflects light radiated from the color center excited by the excitation light and condenses the light in the direction of the optical system. This can obtain higher condensing efficiency of fluorescence and higher absorption efficiency and power density of excitation light. Thus, the responsivity and sensitivity of the diamond magneto-optical sensor can be improved.
(2) The excitation light is emitted to the diamond from the output part of an optical fiber, and the reflecting surface is capable of condensing the radiated light at the output part of the optical fiber. This can obtain higher condensing efficiency of fluorescence and higher absorption efficiency and power density of excitation light. Thus, the responsivity and sensitivity of the diamond magneto-optical sensor can be improved.
(3) A diamond magneto-optical sensor according to a second aspect of the present disclosure includes: a diamond including a color center with an electronic spin, a small portion that allows excitation light propagated through an optical system to be emitted into the diamond, and a reflecting surface that reflects radiated light radiated from the color center excited by the excitation light incident from the small portion and condenses the light in the direction of a light-receiving optical system that guides the light to a light-receiving element, wherein the reflecting surface has a larger area than the small portion and guides the light radiated from the same position in different directions, to the light-receiving optical system through a plurality of optical paths. This can obtain higher condensing efficiency of fluorescence and higher absorption efficiency and power density of excitation light. Thus, the responsivity and sensitivity of the diamond magneto-optical sensor can be improved.
(4) The excitation light may be emitted to the diamond from the output part of the optical fiber through the small portion, and the radiated light may condense at the output part of the optical fiber through the reflecting surface. This can obtain higher condensing efficiency of fluorescence and higher absorption efficiency and power density of excitation light. Thus, the responsivity and sensitivity of the diamond magneto-optical sensor can be improved.
(5) The diamond magneto-optical sensor may further include a member that contains the diamond and allows the passage of the excitation light and the radiated light, and the reflecting surface may be formed on the member. This can reduce the amount of expensive diamond, achieving cost-cutting of the diamond magneto-optical sensor.
(6) The reflecting surface may be formed on the diamond. This can eliminate the need for providing a member as a reflecting surface in addition to the diamond. Furthermore, a large difference in refractive index between the diamond and air allows a critical angle to be smaller on the reflecting surface, so that a compact sensor can be formed with high reflection efficiency.
(7) The reflecting surface may be formed on the member containing the diamond. Thus, the reflecting surface is machined only on the member having higher workability than the diamond, facilitating condensing of excitation light to the diamond. Moreover, a material having a refractive index close to that of the diamond is selected as the member. This can keep a large difference in refractive index from air, facilitate the entry of excitation light into the diamond, and reduce a critical angle on the reflecting surface, so that a compact sensor can be formed with high reflection efficiency.
(8) The reflecting surface may include a curved surface having a focal point or a plurality of planes. This can obtain higher condensing efficiency of fluorescence. In this case, the focal point may be a point of focusing at a position closer than a distance between two different optical paths or more incident on the diamond. The focal point is not limited to a so-called strict optical focal point. Focusing at a geometrical point is preferable, and focusing of a larger number of optical paths is more preferable.
(9) The diamond may have a flat surface and a spherical crown, and the reflecting surface may be formed by the spherical crown. Thus, the shape of the diamond can be easily designed with high condensing efficiency of fluorescence.
(10) The diamond may have two spherical crowns, and the reflecting surface may be formed by the first spherical crown of the two spherical crowns. Thus, the shape of the diamond can be easily designed with high condensing efficiency of fluorescence.
(11) The diamond may be shaped like a polyhedron, and the reflecting surface may be formed by a plurality of faces of the polyhedron. Thus, the diamond can be easily manufactured with high condensing efficiency of fluorescence.
(12) The reflecting surface may have a plane, and an angle formed on the incident side of the excitation light by a plane perpendicular to the incident axis of the excitation light and the plane may be 20° or more and 70° or less. Thus, the diamond can be easily obtained with high condensing efficiency of fluorescence.
(13) The angle formed by the plane perpendicular to the incident axis of the excitation light and the plane may be 30° or more and 50° or less. Thus, the diamond can be easily obtained with higher condensing efficiency of fluorescence.
(14) The diamond may have a corner cube. Thus, the diamond can be easily obtained with higher condensing efficiency of fluorescence.
(15) The member containing the diamond may have a corner cube. Thus, the diamond can be easily obtained with higher condensing efficiency of fluorescence.
(16) The optical system may include an optical fiber, and the size of the diamond may be one third or more and three times or less the core diameter of the optical fiber. Thus, excitation light transmitted through the optical fiber can be efficiently emitted into the diamond, and fluorescence radiated from the diamond can be efficiently emitted into the optical fiber.
(17) The optical system may include an optical fiber, and the size of the diamond may be as large as or larger than a shape inscribed in a circle having the core diameter of the optical fiber and may be as large as or smaller than a shape circumscribed around the circle. Thus, excitation light transmitted through the optical fiber can be efficiently emitted into the diamond, and fluorescence radiated from the diamond can be efficiently emitted into the optical fiber.
(18) The optical system may include an optical fiber and a lens, the excitation light propagated through the optical fiber may be outputted from the lens and emitted into the diamond magneto-optical sensor, the reflecting surface may condense, at the lens, the radiated light radiated from the color center, the magnification of the lens may be the reciprocal of the numerical aperture of the optical fiber, and the size of the diamond may be 80% or more and 120% or less of the product of the core diameter and the numerical aperture of the optical fiber. Thus, excitation light transmitted through the optical fiber can be efficiently emitted into the diamond through the lens, and fluorescence radiated from the diamond can be efficiently inputted to the optical fiber through the lens.
In the following embodiment, the same components are indicated by the same reference numerals. The same components have identical names and functions. Thus, a detailed explanation thereof is not repeated.
Referring to
If a magnetic field or the like is measured by using diamond magneto-optical sensor 100, for example, a face ABC is vertically irradiated with excitation light. Thus, the NV center in diamond magneto-optical sensor 100 is irradiated with the excitation light and fluorescence is radiated. Three faces (specifically, a face ABD, a face BCD, and a face ACD) other than face ABC (that is, an entrance surface) of diamond magneto-optical sensor 100 are polished into flat faces and are allowed to act as reflecting surfaces without providing mirrors (e.g., metallic coating or metallization). Fluorescence radiated in all directions can be internally reflected by face ABD, face BCD, and face ACD of diamond magneto-optical sensor 100, can be outputted from face ABC, and can be detected by a detector.
Angles α, β, and γ of diamond magneto-optical sensor 100 are freely set. Angles α, β, and γ are all preferably set at 90°. In this case, the shape of diamond magneto-optical sensor 100 is called a corner cube. Sides a, b, and c of diamond magneto-optical sensor 100 preferably satisfy 0.5b≤a≤1.5b and 0.5c≤a≤1.5c.
Referring to
Optical fiber 102 only needs to be disposed next to (or in contact with) diamond magneto-optical sensor 100. Optical fiber 102 is preferably disposed with the optical axis located perpendicular to face ABC (that is, the entrance surface) of diamond magneto-optical sensor 100. Light (e.g., a wavelength of about 532 nm) outputted from a light source (e.g., a laser diode) is transmitted through optical fiber 102 as the excitation light of an NV center 104 of diamond magneto-optical sensor 100 and enters diamond magneto-optical sensor 100. Fluorescence emitted from NV center 104 is internally reflected by the reflecting surfaces (that is, face ABD, face BCD, and face ACD) of diamond magneto-optical sensor 100 as described above, is outputted from face ABC, and is transmitted to the detector through optical fiber 102.
At this point, if diamond has a refractive index of 2.4, the total reflection of a material with a refractive index of 2.4 has a critical angle of 24.6°, so that an angle θ(°) formed by a reflecting surface 106 (that is, face ABD) of diamond magneto-optical sensor 100 and a vertical plane 108 perpendicular to the optical axis of optical fiber 102 preferably satisfies 20≤θ≤70 (45−25≤θ≤45+25). For the reflecting surfaces, θ is set in this range (that is, diamond magneto-optical sensor 100 is formed with θ set in this range), so that light incident on the reflecting surfaces in diamond magneto-optical sensor 100 can be reflected to the front of diamond magneto-optical sensor 100 and in the direction of the central axis of optical fiber 102. This can increase the ratio of excitation light used for exciting the NV center and increase the ratio of fluorescence emitted into optical fiber 102. More preferably, 24.6≤θ≤65.4 (45−20.4≤θ≤45+20.4) is satisfied. Still more preferably, 38≤θ≤52 (45−(20.4/3)≤θ≤45+(20.4/3)) is satisfied.
The size of diamond magneto-optical sensor 100 is preferably one third or more and three times or less of the core diameter (that is, the diameter of the core) of optical fiber 102. The size of diamond magneto-optical sensor 100 means, for example, the size of the circumcircle of a surface facing optical fiber 102 (that is, the entrance surface of excitation light). Moreover, it is preferable that the size of diamond magneto-optical sensor 100 is as large as or larger than a shape inscribed in a circle having the core diameter of optical fiber 102 and is as large as or smaller than a shape circumscribed around the circle. Thus, excitation light transmitted through optical fiber 102 can be efficiently emitted into diamond magneto-optical sensor 100 and fluorescence radiated from diamond magneto-optical sensor 100 can be efficiently emitted into the core of optical fiber 102.
Furthermore, a condensing element may be disposed between diamond magneto-optical sensor 100 and optical fiber 102. For example, referring to
The magnification of a lens composed of condensing elements 110 and 112 is preferably the reciprocal of a numerical aperture NA (that is, 1/NA) of optical fiber 102. The size of diamond magneto-optical sensor 100 is preferably 80% or more and 120% or less of the product of a core diameter ϕ and numerical aperture NA of optical fiber 102 (that is, ϕ×NA). Thus, excitation light transmitted through optical fiber 102 can be efficiently emitted into diamond magneto-optical sensor 100 and fluorescence radiated from diamond magneto-optical sensor 100 can be efficiently emitted into the core of optical fiber 102.
In the foregoing description, excitation light and fluorescence are transmitted through optical fiber 102. The configuration is not limited thereto. Optical fiber 102 may be replaced with a light guide that is a bundle of a plurality of optical fiber cores.
The optical path for excitation light reflected by the plurality of reflecting surfaces to NV center 104 is longer (e.g., by about twice) than an optical path for excitation light directly radiated to NV center 104 without being reflected by the reflecting surfaces. Thus, the optical path for excitation light in diamond magneto-optical sensor 100 can be brought close to the absorption length of diamond, thereby increasing the absorption efficiency (that is, the quantum efficiency of absorption) of excitation light. In other words, since the number of NV centers for excitation increases, the intensity of radiated fluorescence rises. This can improve the sensitivity of the diamond magneto-optical sensor.
Referring to
As described above, about 2.3% of fluorescence radiated forward from the NV center can be observed in the flat diamond in
Thus, diamond magneto-optical sensor 100 can improve the condensing efficiency of fluorescence and the absorption efficiency and power density of excitation light. Thus, the diamond magneto-optical sensor can be obtained with higher responsivity and sensitivity.
In the foregoing description, the diamond magneto-optical sensor is formed from a diamond. The configuration is not limited thereto. Members other than diamond may be included. A diamond magneto-optical sensor according to a first modification includes members other than a diamond.
Referring to
As described above, fluorescence radiated from the NV center of diamond 122 is reflected by reflecting surface 128 and is outputted from entrance surface 126. The member containing diamond 122 is not limited to glass. Any members may be used if the transmittances of green light (that is, a wavelength of about 490 to 560 nm) and red light (that is, a wavelength from about 630 to 800 nm) are high. The member may be made of resin. Since the refractive index of glass 124 is lower than that of diamond, reflecting surface 128 is preferably surface-machined and provided with a mirror (e.g., metallic coating or metallization).
In the foregoing description, the reflecting surface is flat. The configuration is not limited thereto. A diamond magneto-optical sensor according to a second modification has a curved reflecting surface.
Referring to
Furthermore, the reflecting surface of the diamond magneto-optical sensor may be a spherical surface. Referring to
The diamond magneto-optical sensor according to the second modification may be formed to include a diamond including an NV center and a glass containing the diamond as in the first modification. In this case, the glass containing the diamond is shaped as illustrated in
In the foregoing description, the entrance surface of excitation light is flat. The configuration is not limited thereto. A diamond magneto-optical sensor according to a third modification has a curved entrance surface.
Referring to
If reflecting surface 154 is formed by two spherical segments obtained by cutting a sphere with a radius r as illustrated in
The diamond magneto-optical sensor according to the third modification may be formed to include a diamond including an NV center and a glass containing the diamond as in the first modification. In this case, the glass containing the diamond is shaped as illustrated in
In the foregoing description, the diamond magneto-optical sensor is a tetrahedron. The shape is not limited thereto. The diamond magneto-optical sensor according to a fourth modification is a polyhedron having five faces or more.
Referring to
If a magnetic field is measured by using diamond magneto-optical sensor 160, an angle δ in
g×(1/1.4-0.5)≤f≤g×(1/1.4+0.5)
h×(1/1.4-0.5)≤f≤h×(1/1.4+0.5)
i×(1/1.4-0.5)≤f≤i×(1/1.4+0.5)
The diamond magneto-optical sensor may be a polyhedron having six faces or more. The curved reflecting surfaces in
The diamond magneto-optical sensor according to the fourth modification may be formed to include a diamond including an NV center and a glass containing the diamond as in the first modification. In this case, the glass containing the diamond is shaped like a polyhedron having five faces or more (for example, the triangular pole in
In the foregoing description, fluorescence outputted from the entrance surface of excitation light is detected (that is, the incident direction of excitation light into the diamond magnetic sensor and the output direction of fluorescence from the diamond magnetic sensor are opposite to each other) in the diamond magnetic sensor. The configuration is not limited thereto. In a diamond magneto-optical sensor according to a fifth modification, the incident direction of excitation light and the output direction of fluorescence agree with each other and fluorescence outputted from a surface different from the entrance surface of excitation light is detected.
Referring to
Referring to
Small portion 402 having a smaller area than reflecting surface 404 only needs to satisfy optical conditions of incidence on diamond magneto-optical sensor 400 and may have a nonflat surface as will be described later. Small portion 402 preferably has a size of sub μm or more so as to be irradiated with a laser beam (that is, excitation light). Moreover, small portion 402 is preferably located such that radiated light (that is, fluorescence) from the NV center by excitation light having entered diamond magneto-optical sensor 400 can be reflected by the reflecting surface and condensed toward an optical system that receives the radiated light. Condensing means the function of concentrating light with an increased angle to a desired direction.
In the foregoing description, small portion 402 for receiving excitation light is flat. The configuration is not limited thereto. Referring to
In the fifth modification, the diamond magnetic sensor including the NV center is shaped like a triangular pyramid with a small portion. The configuration is not limited thereto. Referring to
As in the fifth modification, the small portion may be flat. Referring to
In the fifth and sixth modifications, the diamond magnetic sensor is entirely made of diamond. The configuration is not limited thereto. Referring to
The small portion formed on the glass may have a nonflat surface. Referring to
As described above, diamond 122 only needs to be sized such that at least a part of diamond 122 is present in the excitation light increasing area (that is, inside a chain line in
The shape of the glass containing the diamond is not limited to the foregoing shape. Referring to
The small portion of the glass may be flat. Referring to
The glass is preferably quartz glass in view of the transmittance of light, workability, and ease of handling. More preferably, the glass is a material that can transmit 90% or more of excitation light and fluorescence and has a high refractive index. This is because a critical angle for total reflection increases on a glass reflecting surface (e.g., reflecting surface 456 in
A sensor unit can be formed by using the diamond magneto-optical sensor. Specifically, as described above, the sensor unit includes a diamond magneto-optical sensor including an NV center, an irradiation unit that irradiates the diamond magneto-optical sensor with excitation light, a detection unit that detects radiated light from the NV center of the diamond magneto-optical sensor, and an optical waveguide that transmits excitation light and radiated light. Thus, the sensor unit with high responsivity and sensitivity can be achieved.
In the foregoing description, the diamond magneto-optical sensor includes the NV center. The configuration is not limited thereto. The diamond magneto-optical sensor only needs to include a color center with an electronic spin. The color center with the electronic spin is a center that forms a spin triplet state and is illuminated by excitation. A typical example is the color center is an NV center. Additionally, it is known that a color center with an electronic spin is also present in a silicon-vacancy center (that is, Si-V center), a germanium-vacancy center (that is, Ge-V center), and a tin-vacancy center (that is, Sn-V center). Thus, the diamond magneto-optical sensor may be formed by using diamonds including such centers instead of a diamond including an NV center.
In the foregoing description, excitation light and fluorescence are transmitted to the diamond magneto-optical sensor through the optical fiber. The configuration is not limited thereto. Excitation light and fluorescence may be spatially transmitted. For example, referring to
The effectiveness of the present disclosure will be described below according to an example. For the diamond magneto-optical sensor, an element cut in the shape of a corner cube in
A diamond of type Ib was used. Electrons were injected into the diamond with an electron acceleration energy of 3 MeV and an electron dose of 3×1018/cm2, and then the diamond was annealed at 800° C. for about one hour, so that the diamond including an NV center was generated. The diamond was cut into a corner cube with an oblique side of 1 mm to produce a diamond magneto-optical sensor. Moreover, the diamond was cut into a cube with a side of 1 mm to produce a diamond magneto-optical sensor as a comparative example.
By using a measuring device configured as illustrated in
For light source 200 for generating excitation light, an LD (laser diode) element (specifically, L515A1 of Thorlabs, Inc.) was used, and a green laser beam (that is, excitation light) of 5 mW was generated. Excitation light outputted from light source 200 was condensed through collimate lens 202 and then was emitted to dichroic mirror 204. For collimate lens 202, LA1116-A of Thorlabs, Inc. was used. For dichroic mirror 204, S06-RG of SURUGA SEIKI Co., Ltd. was used. Excitation light (that is, green light) incident on dichroic mirror 204 is reflected by dichroic mirror 204. The reflected light was condensed through sphere lens 206, was caused to enter optical fiber 208 (specifically, the core), was transmitted through optical fiber 208, and then was emitted to diamond magneto-optical sensor 210. For sphere lens 206, MS-08-4.35P1 (8 mm in diameter) of OptoSigma Corporation was used. For optical fiber 208, an optical digital cable having a core diameter ϕ of 0.9 mm was used.
In fluorescence radiated from diamond magneto-optical sensor 210, fluorescence having entered optical fiber 208 is propagated through optical fiber 208, is transformed into parallel rays through sphere lens 206, and then is emitted to dichroic mirror 204. Fluorescence (that is, red light) incident on dichroic mirror 204 passes through dichroic mirror 204 and enters LPF 212. Fluorescence having passed through LPF 212 was detected by photodetector 214. LPF 212 allows the passage of light at a predetermined wavelength or longer and cuts (e.g., reflects) light at a wavelength shorter than the predetermined wavelength. For LPF 212, LOPF-25C-593 of OptoSigma Corporation was used. For photodetector 214, a photodiode (specifically, S6967 of Hamamatsu Photonics K.K.) was used. Radiated light of diamond is red light passing through LPF 212, whereas excitation light having a shorter wavelength than red light does not pass through LPF 212. Thus, excitation light emitted from light source 200 was detected as noise by photodetector 214, thereby suppressing a reduction in the sensitivity of detection.
Microwaves (1 W) generated by a microwave generator (not illustrated) were transmitted to diamond magneto-optical sensor 210 by using coaxial cable 220 and microwave irradiation unit 222. For coaxial cable 220, a coaxial cable with a characteristic impedance of 50Ω was used. Referring to
The measurement results are shown in
According to the result of
As in Example 1, for the diamond magneto-optical sensor, an element cut in the shape of a corner cube in
A diamond magneto-optical sensor was produced as in Example 1. Specifically, a diamond of type Ib was used. Electrons were injected into the diamond with an electron acceleration energy of 3 MeV and an electron dose of 3×1018/cm2, and then the diamond was annealed at 800° C. for about one hour, so that the diamond including an NV center was generated. The diamond was cut into a corner cube with an oblique side of 1 mm, and a small portion (that is, a portion where excitation light is incident on the diamond) was formed at an apex of the cube, so that a diamond magneto-optical sensor was produced. Moreover, the diamond was cut into a cube with a side of 1 mm to produce a diamond magneto-optical sensor as a comparative example.
By using a measuring device configured as illustrated in
Light source 200, collimate lens 202, and photodetector 214 were identical to those of Example 1. Unlike in Example 1, FGL590 of Thorlabs, Inc. was used for LPF 212. For coaxial cable 220, a coaxial cable with a characteristic impedance of 50Ω was used as in Example 1. λ/4 transformer 520 included a microstrip line with an impedance of 20Ω. λ/4 open stub 522 included parallel two lines with an impedance of 300Ω. λ/4 transformer 520 acted as an impedance converter, accurately converted an impedance between coaxial cable 220 and λ/4 open stub 522 acting as a resonator, and efficiently irradiated the diamond magneto-optical sensor 210 with microwaves.
Green light of 5 mW was emitted as excitation light. The spot of the excitation light was reduced to a diameter of 20 μm with a power density of 3 W/mm2. The frequencies of microwaves of 1 W were swept in the range of 2.74 GHz to 2.94 GHz, excitation light was emitted to diamond magneto-optical sensor 210, and generated fluorescence was measured. Consequently, a response speed of 30 us was obtained in both of the diamond cut in a corner cube and the diamond of the comparative example. A photocurrent in the photodiode of photodetector 214 was 10 μA, which corresponds to the intensity of fluorescence, in the diamond of the comparative example, whereas a photocurrent of 100 μA was obtained in the diamond cut in a corner cube.
The present disclosure was described according to the description of the embodiment. The embodiment was merely exemplary and the present disclosure is not limited to the embodiment. The scope of the present disclosure is indicated by the claims in consideration of the detailed description of the invention. The scope of the present disclosure includes meanings equivalent to the language of the claims and all changes in the scope.
Number | Date | Country | Kind |
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2021-059798 | Mar 2021 | JP | national |
Filing Document | Filing Date | Country | Kind |
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PCT/JP2022/015393 | 3/29/2022 | WO |