A biological component measurement apparatus includes an optical medium, a high thermal conductive film, an excitation light source, a probe light source, and a light position detector. The high thermal conductive film is higher in thermal conductivity than the optical medium, and is provided on a sample placement surface of the optical medium. The high thermal conductive film spreads heat generated from the sample irradiated with excitation light more in a first direction than in a second direction. The first direction is a traveling direction of probe light in plan view of the sample placement surface. The second direction is a direction orthogonal to the first direction in plan view of the sample placement surface.

Systems and methods are provided for performing photothermal dynamic imaging. An exemplary method includes: scanning a sample to produce a plurality of raw photothermal dynamic signals; receiving the raw photothermal dynamic signals of the sample; generating a plurality of second signals by matched filtering the raw photothermal dynamic signals to reject non-modulated noise; and performing an inverse operation on the second signals to retrieve at least one thermodynamic signal in a temporal domain.

Mid-infrared photothermal heterodyne imaging (MIR-PHI) techniques described herein overcome the diffraction limit of traditional MIR imaging and uses visible photodiodes as detectors. MIR-PHI experiments are shown that achieve high sensitivity, sub-diffraction limit spatial resolution, and high acquisition speed. Sensitive, affordable, and widely applicable, photothermal imaging techniques described herein can serve as a useful imaging tool for biological systems and other submicron-scale applications.

Asymmetric interferometry is used with various embodiments of Optical Photothermal Infrared (OPTIR) systems to enhance the signal strength indicating the photothermal effect on a sample.

A method comprises non-destructive contact-free physical characterization of a sample by repeated excitations of the surface of a sample with a sequence of pulses comprising at least one pump pulse by a first “pump” laser followed by a succession of L temporarily offset pulses by a second “probe” laser, and the analysis of the beam emitted by the surface of the sample by an activated photodetector, for the acquisition of signals delivered by the photodetectors during constant time windows.

System for performing chemical spectroscopy on samples from the scale of nanometers to millimeters or more with a multifunctional platform combining analytical and imaging techniques including dual beam photo-thermal spectroscopy with confocal microscopy, Raman spectroscopy, fluorescence detection, various vacuum analytical techniques and/or mass spectrometry. In embodiments described herein, the light beams of a dual-beam system are used for heating and sensing.

A passive-phase-detection photothermal spectroscopy (PTS) system and methods are provided for gas measurements. The PTS system includes a pump laser source, a probe laser source, the pump and probe laser beams simultaneously propagating through an optical waveguide having a target gas specimen. Moreover, the PTS system can be based on a heterodyne detection scheme and includes a combiner configured to align light input from a local oscillator with the probe laser beam output from the optical waveguide to output to a photodetector that is configured to generate beat notes. A demodulation module is configured to detect and measure a photothermal signal based on the beat notes received from the photodetector for gas measurements. The PTS system can also be based on a core-cladding-mode interference detection scheme and generates the core mode and cladding mode simultaneously for the probe laser in the waveguide.

A biological component measurement apparatus includes an optical medium, an excitation light source, a probe light source, and a light position detector. The optical medium includes a sample placement surface. The excitation light source emits excitation light toward a sample placed on the sample placement surface. The probe light source emits probe light that travels through the optical medium. The light position detector detects the position of the probe light outgoing from the optical medium. The optical medium is formed from chalcogenide glass.

Systems and methods for detecting photothermal effect in a sample are described herein. In these systems and methods, a pump source is configured to generate a pump pulse train, a probe source is configured to generate a probe pulse train and is synchronized with the pump pulse train, and a camera collects the resulting data. The camera is configured to collect a first signal corresponding to a hot frame, wherein the hot frame includes visible probe beam as modified by a pump beam and a second signal corresponding to a cold frame, wherein the cold frame includes visible probe beam that has not been modified by a pump beam. A processor can subtract the second signal from the first signal to detect the photothermal effect.

Apparatus and methods for measuring infrared absorption of a sample that includes delivering a pulse of infrared radiation to a region of the sample, delivering pulses of radiation of a shorter wavelength than infrared radiation to a sub-region within the region, and using one or more properties of the induced photoacoustic signals to create a signal indicative of infrared absorption of the sub-region of the sample.