An electrically modulated light source is provided. The electrically modulated light source comprises a carbon nanotube film structure. The electrically modulated light source heats up to a highest temperature and emits thermal radiation in less than 10 milliseconds after a voltage is applied, and the electrically modulated light source cools down to an initial temperature of the electrically modulated light source in less than 10 milliseconds after the voltage is removed. An modulation frequency of the electrically modulated light source is greater than or equal to 150 KHz. A non-dispersive infrared spectrum detection system used the electrically modulated light source, and a method for detecting gas used the electrically modulated light source are also provided.

Method and gas analyzer for measuring the concentration of a gas component in a sample gas, wherein to measure the concentration of a gas component in a sample gas, a laser diode is actuated by a current and light generated by the laser diode is guided through the sample gas to a detector, the current is simultaneously varied within periodically successive sampling intervals for the wavelength-dependent sampling of an absorption line of interest of the gas component, and the current can be additionally modulated sinusoidally based on wavelength modulation spectroscopy with a low frequency and small amplitude, such that a measuring signal generated by the detector is evaluated to form a measurement result, where to improve the measuring signal-noise ratio and achieve a much lower detection limit with the same measuring distance, the current is modulated with a high (RF) frequency in the GHz range so that no wavelength modulation occurs, and an RF modulation amplitude is selected at the maximum level using the linear control range of the laser diode where, before evaluation, the measuring signal is demodulated at the radio frequency.

A reaction processing apparatus includes: a reaction processing vessel; a first fluorescence detection device that irradiates a sample with first excitation light and detects first fluorescence produced from the sample; and a second fluorescence detection device that irradiates a sample with second excitation light and detects second fluorescence produced from the sample. The wavelength range of the first fluorescence and the wavelength range of the second excitation light overlap at least partially. The first excitation light and the second excitation light flash at a predetermined duty ratio d. The phase difference between the flashing of the first excitation light and the flashing of the second excitation light is set within a range of 2π(pm−Δpm) (rad) to 2π(pm+Δpm) (rad) or within a range of 2π[(1−pm)−Δpm] (rad) to 2π[(1−pm)+Δpm] (rad), where pm=d−d2 and Δpm=0.01*pm.

Analyte collection and testing systems and methods, and more particularly to testing systems and methods that achieve significant improvements in the detection of fluorescence signals in the reader by modulating the applied optical excitation. Also described herein are optical detection apparatuses and methods for removable photonic chips that do not require translation for calibration when coupling the photonics chip with the sensing system. Also described herein are methods and apparatuses for accurately calibrating a dilution factor when reading from a photonics chip.

A measurement system is provided with an array of laser diodes with one or more Bragg reflectors. At least a portion of the light generated by the array is configured to penetrate tissue comprising skin. A detection system configured to: measure a phase shift, and a time-of-flight, of at least a portion of the light from the array of laser diodes reflected from the tissue relative to the portion of the light generated by the array; generate one or more images of the tissue; detect oxy- or deoxy-hemoglobin in the tissue; non-invasively measure blood in blood vessels within or below a dermis layer within the skin; measure one or more physiological parameters based at least in part on the non-invasively measured blood; and measure a variation in the blood or physiological parameter over a period of time.

An active remote sensing system is provided with an array of laser diodes that generate light directed to an object having one or more optical wavelengths that include at least one near-infrared wavelength between 600 nanometers and 1000 nanometers. One of the laser diodes pulses at a modulation frequency between 10 Megahertz and 1 Gigahertz and has a phase associated with the modulation frequency. A detection system includes a photo-detector, a lens, a spectral filter at an input to the photo-detector, and a processor that processes digitized signals received from the photo-detector to generate an output signal. The detection system uses a lock-in technique that synchronizes pulsing the one laser diode. The active remote sensing system is configured to be mounted on a vehicle or an airborne platform to provide distance information based on a time-of-flight measurement.

A gas analysis system, includes: a light-emitting element that emits a laser light modulated by a predetermined modulation frequency; and a light-receiving element that: receives the laser light that has passed through a measurement target gas; and upon receiving the laser light, outputs a received signal having an N-frequency that is n times the predetermined modulation frequency, wherein n is an integer no less than 2; and a signal processing device that: calculates a third component by removing, from a first component having the N-frequency, a second component, wherein the second component is a component of optical interference noise arising on an optical path of the laser light from the light-emitting element to the light-receiving element and has the same frequency as the first component; and calculates, based on a magnitude of the third component, a concentration of the measurement target gas.

Systems for measuring optical properties of a specimen are disclosed. The systems are configured to sample signals related to the measurement of the properties of a specimen, and perform software-based coherent detection of the signals to generate resulting measurements are based on the signals acquired at substantially the same time instance. This facilitates the displaying or generating of the desired measurements in real time. In one configuration, the system is configured to direct a modulated light signal at a selected wavelength incident upon a specimen. In another configuration, the system is configured to direct a combined light signal, derived from a plurality of light signals at different wavelengths and modulated with different frequencies, incident upon a specimen. In yet another configuration, the system is configured to direct a plurality of light signals modulated with different frequencies incident upon different regions of a specimen.

Optogenetic systems and methods for probing a specimen using spatio-temporally modulated illumination light are disclosed. A method may include generating illumination light, the illumination light including a plurality of illumination protocols temporally sampled and interleaved with one another at a time-division-multiplexed (TDM) sampling rate, each illumination protocol being for illuminating a respective region of interest (ROI) of a plurality of ROIs of the specimen. The illumination light may include either activation or excitation light, or both. The method may also include applying a spatio-temporal modulation to the illumination light and directing the resulting modulated illumination light onto the specimen. The modulation may include repeatedly imparting, at a pattern switching rate matched and synchronized with the TDM sampling rate, a sequence of a plurality of spatial modulation patterns to the plurality of temporally sampled and interleaved illumination protocols, each spatial modulation pattern mapping to a respective one of the ROIs.

In an analysis device that irradiates light from three or more light sources onto a cell, embodiments proposed herein prevent a reduction in the intensity of light from each light source, and are provided with at least a first light source, a second light source, and a third light source, and an optical system that guides light from the respective light sources onto a cell. The optical system is provided with a second light source optical element that reflects the light from the first light source and transmits the light from the second light source, and a third light source optical element that reflects the light from the first light source that has been reflected by the second light source optical element and the light from the second light source that has been transmitted through the second light source optical element, and transmits the light from the third light source.