Patent classifications
H01S1/06
Acquisition of Interferometric Recordings of Brain and Neuron Activity by Coherent Microwave Probe With Therapeutic Activation, Inactivation, or Ablation of Molecular, Neuronal or Brain Targets
Low power MASER (Microwave Amplification by Stimulated Emission of Radiation) radiation is used to non-invasively record molecular activity in a biological object such as a brain. Low power MASER radiation is also used to neuromodulate molecular targets via Rabi coupling, resulting for example in conformational and function change in specific molecular targets such as ligand-gated ion channels, voltage-gated ion channels, G-proteins, or dopamine receptors. The method can be used to change the energy state of targeted molecules via energization or enervation, or to ablate targeted molecules.
Acquisition of Interferometric Recordings of Brain and Neuron Activity by Coherent Microwave Probe With Therapeutic Activation, Inactivation, or Ablation of Molecular, Neuronal or Brain Targets
Low power MASER (Microwave Amplification by Stimulated Emission of Radiation) radiation is used to non-invasively record molecular activity in a biological object such as a brain. Low power MASER radiation is also used to neuromodulate molecular targets via Rabi coupling, resulting for example in conformational and function change in specific molecular targets such as ligand-gated ion channels, voltage-gated ion channels, G-proteins, or dopamine receptors. The method can be used to change the energy state of targeted molecules via energization or enervation, or to ablate targeted molecules.
ATOMIC FREQUENCY OBTAINING DEVICE AND ATOMIC CLOCK
[Problem] To provide an atomic frequency obtaining device which enables an improvement in mass-productivity and a reduction in size, and an atomic clock which uses the atomic frequency obtaining device.
[Solution] A laser light source 20, a vapor cell unit 30 that includes a vapor cell 31 in which atomic gas was enclosed, and a light detector 40 are provided on a circuit board 10. Light emitted from the laser light source 20 is reflected by a first reflective member 51 so that the direction in which the light travels is changed and the light passes through the vapor cell. The light passes through the vapor cell 31, and is reflected by a second reflective member 52 so that the direction in which the light travels is changed and the light travels toward the light detector 40.
Atomic resonator
This atomic resonator for causing a resonance frequency by CPT resonance includes: a gas cell having alkali metal atoms enclosed; a photodetector configured to detect light having passed through the gas cell and convert the light to an electric signal; a high-frequency oscillator configured to receive the electric signal and output the signal after a frequency thereof is divided by two; and a laser light source configured to modulate and introduce, into the gas cell, light based on the signal output from the high-frequency oscillator. The high-frequency oscillator has an injection-locked frequency divider circuit including an acoustic resonator as an oscillation element.
Phased-array MASER detector for synthetic aperture interferometric imaging
A phased-array MASER detector for synthetic aperture interferometric three-dimensional imaging. The detector elements, for example 10.sup.2-10.sup.6 zero bias Schottky detector diodes with sufficient sensitivity to reliably detect various values of MASER radiation, are arranged in layers offset in three dimensions. The phased-array MASER detector is particularly useful for detecting characteristics in a biological object using low energy (2-10 Watts), coherent MASER radiation. MASER intensity data of an interferometric pattern is collected by the detector array, is deconvolved, and is used to generate three-dimensional energy activity maps for a given time slice or on a time-shifting basis.
Phased-array MASER detector for synthetic aperture interferometric imaging
A phased-array MASER detector for synthetic aperture interferometric three-dimensional imaging. The detector elements, for example 10.sup.2-10.sup.6 zero bias Schottky detector diodes with sufficient sensitivity to reliably detect various values of MASER radiation, are arranged in layers offset in three dimensions. The phased-array MASER detector is particularly useful for detecting characteristics in a biological object using low energy (2-10 Watts), coherent MASER radiation. MASER intensity data of an interferometric pattern is collected by the detector array, is deconvolved, and is used to generate three-dimensional energy activity maps for a given time slice or on a time-shifting basis.
Acquisition of interferometric recordings of brain and neuron activity by coherent microwave probe with therapeutic activation, inactivation, or ablation of molecular, neuronal or brain targets
Low power MASER (Microwave Amplification by Stimulated Emission of Radiation) radiation is used to non-invasively record molecular activity in a biological object such as a brain. Low power MASER radiation is also used to neuromodulate molecular targets via Rabi coupling, resulting for example in conformational and function change in specific molecular targets such as ligand-gated ion channels, voltage-gated ion channels, G-proteins, or dopamine receptors. The method can be used to change the energy state of targeted molecules via energization or enervation, or to ablate targeted molecules.
Acquisition of interferometric recordings of brain and neuron activity by coherent microwave probe with therapeutic activation, inactivation, or ablation of molecular, neuronal or brain targets
Low power MASER (Microwave Amplification by Stimulated Emission of Radiation) radiation is used to non-invasively record molecular activity in a biological object such as a brain. Low power MASER radiation is also used to neuromodulate molecular targets via Rabi coupling, resulting for example in conformational and function change in specific molecular targets such as ligand-gated ion channels, voltage-gated ion channels, G-proteins, or dopamine receptors. The method can be used to change the energy state of targeted molecules via energization or enervation, or to ablate targeted molecules.
HERMETIC VIAL FOR QUANTUM TRANSITIONS DETECTION IN ELECTRONIC DEVICES APPLICATIONS
A physics cell includes a sealed glass vial that contains a high-purity dipolar gas (e.g., OCS) at a low pressure (e.g., between about 0.01 millibar and 0.2 millibar). The vial can be sealed using a laser cutting process that involves only local heating of the vial that does not denature the bulk of the contained gas. One or more electromagnetically translucent windows or vial-end access points provide access to electromagnetic waves launched or received by one or more electromagnetic antennas at a frequency that is adjusted to match the quantum transition frequency of the gas based on a detected maximum absorption frequency. The glass-vial physics cell can be fabricated at lower cost than physics cells fabricated from bonded wafers. Multiple vials can be joined by a waveguide in an enclosure so that launch and receive antennas can be provided at a single end of the vials.
HERMETIC VIAL FOR QUANTUM TRANSITIONS DETECTION IN ELECTRONIC DEVICES APPLICATIONS
A physics cell includes a sealed glass vial that contains a high-purity dipolar gas (e.g., OCS) at a low pressure (e.g., between about 0.01 millibar and 0.2 millibar). The vial can be sealed using a laser cutting process that involves only local heating of the vial that does not denature the bulk of the contained gas. One or more electromagnetically translucent windows or vial-end access points provide access to electromagnetic waves launched or received by one or more electromagnetic antennas at a frequency that is adjusted to match the quantum transition frequency of the gas based on a detected maximum absorption frequency. The glass-vial physics cell can be fabricated at lower cost than physics cells fabricated from bonded wafers. Multiple vials can be joined by a waveguide in an enclosure so that launch and receive antennas can be provided at a single end of the vials.