arXiv subjects

Takuro Ideguchi

Publications and source records attributed to Takuro Ideguchi.

At least 37 records · Page 2Linked to original sources

arXiv2021

A simple approach of broadband mid-infrared pulse generation with a mode-locked Yb-doped fiber laser

Broadband mid-infrared (MIR) molecular spectroscopy demands a bright and broadband light source in the molecular fingerprint region. To this end, intra-pulse difference frequency generation (IDFG) has shown excellent properties among various techniques. However, previous IDFG systems have mainly used unconventional long-wavelength 2-$μ$m ultrashort pulsed lasers. A few systems have been demonstrated with 1-$μ$m lasers, but they use bulky 100-W-class high-power Yb thin-disk lasers. In this work, we demonstrate a simple and robust approach of 1-$μ$m-pumped broadband IDFG with a conventional mode-locked Yb-doped fiber laser. We first generate 3.3-W, 12.1-fs ultrashort pulses at 50 MHz by a simple combination of spectral broadening with a short single-mode fiber and pulse compression with chirped mirrors. Then, we use them for pumping a thin orientation-patterned gallium phosphide (OP-GaP) crystal, generating 1.2-mW broadband MIR pulses with the -20-dB bandwidth of 480 cm$^{-1}$ in the fingerprint region (760-1240 cm$^{-1}$, 8.1-13.1 $μ$m). The 1-$μ$m-based IDFG system allows for simultaneous generation of ultrashort pulses in the ultraviolet and visible regions, enabling, for example, 100-MHz-level high-repetition-rate vibrational sum-frequency generation spectroscopy or pump-probe spectroscopy.

physics.optics↗

arXiv2021

Broadband complementary vibrational spectroscopy with cascaded intra-pulse difference frequency generation

One of the essential goals of molecular spectroscopy is to measure all fundamental molecular vibrations simultaneously. To this end, one needs to measure broadband infrared (IR) absorption and Raman scattering spectra, which provide complementary vibrational information. A recently demonstrated technique called complementary vibrational spectroscopy (CVS) enables simultaneous measurements of IR and Raman spectra with a single device based on a single laser source. However, the spectral coverage was limited to ~1000 cm-1, which partially covers the spectral regions of the fundamental vibrations. In this work, we demonstrate a simple method to expand the spectral bandwidth of the CVS with a cascaded intra-pulse difference-frequency generation (IDFG). Using the system, we measure broadband CVS spectra of organic liquids spanning over 2000 cm-1, more than double the previous study.

physics.optics↗

arXiv2021

Compressive dual-comb spectroscopy

Broadband, high resolution and rapid measurement of dual-comb spectroscopy (DCS) generates a large amount of data stream. We numerically demonstrate significant data compression of DCS spectra by using a compressive sensing technique. Our numerical simulation shows a compression rate of more than 100 with 3% error in mole fraction estimation of mid-infrared (MIR) DCS of two molecular species in a broadband (~30 THz) and high resolution (~115 MHz) condition. We also numerically demonstrate a massively parallel MIR DCS spectrum of 10 different molecular species can be reconstructed with a compression rate of 10.5 with a transmittance error of 0.003 from the original spectrum.

eess.SP↗

arXiv2020

High-speed Fourier-transform infrared spectroscopy with phase-controlled delay line

Fourier-transform infrared spectroscopy (FTIR) is the golden standard of mid-infrared (MIR) molecular spectroscopic analysis through optically-encoded vibrational signatures. Michelson-type FTIR and MIR dual-comb spectrometers allow us to simultaneously investigate multiple molecular species via the broadband and high-resolution spectroscopic capabilities. However, these are not applicable to high-speed measurements due to the low temporal resolution which is fundamentally limited by the signal-to-noise ratio (SNR). In this study, we develop a high-speed FTIR spectroscopy technique called phase-controlled Fourier-transform infrared spectroscopy (PC-FTIR) that has the capability to measure MIR absorption spectra at a rate of above 10 kHz. PC-FTIR demonstrates the high scan rate with a high SNR for various spectral bandwidths by arbitrarily adjusting the instrumental spectral resolution. As a proof of principle demonstration, we measure high-speed mixing dynamics of two liquids at a rate of 24 kHz. We also measure MIR spectra of gas-phase molecules with higher spectral resolution at a rate of 12 kHz. This high-speed MIR spectrometer could be especially useful for measuring non-repetitive fast phenomena and acquiring a large amount spectral data within a short time.

physics.optics↗

arXiv2020

Time-stretch infrared spectroscopy

Improving spectral acquisition rate of broadband mid-infrared spectroscopy promises further advancements of molecular science and technology. Unlike the pump-probe spectroscopy that requires repeated measurements with different pump-probe delays, continuous spectroscopy running at a high spectral acquisition rate enables transient measurements of rapidly changing non-repeating phenomena or statistical analysis of a large amount of spectral data acquired within a short time. Recently, Fourier-transform infrared spectrometers (FT-IR) with rapid delay scan mechanisms including dual-comb spectrometers have significantly improved the measurement rate up to ~1 MSpectra/s that is fundamentally limited by the signal-to-noise ratio. Here, we overcome the limit and demonstrate the fastest continuous broadband vibrational spectrometer running at 80 MSpectra/s by implementing wavelength-swept time-stretch spectroscopy technique in the mid-infrared region. Our proof-of-concept experiment of the time-stretch infrared spectroscopy (TS-IR) demonstrates broadband absorption spectroscopy of phenylacetylene from 4.4 to 4.9 μm (2040-2270 cm-1) at a resolution of 15 nm (7.7 cm-1) with a superior signal-to-noise ratio of 85 without averaging and a shot-to-shot fluctuation of 1.3%.

physics.optics↗

arXiv2020

A multimodal laser-scanning nonlinear optical microscope with a rapid broadband Fourier-transform coherent Raman modality

Nonlinear optical microscopy allows rapid high-resolution microscopy with image contrast generated from intrinsic properties of the sample. Established modalities such as multiphoton excited fluorescence and second/third-harmonic generation can be combined with other nonlinear techniques, such as coherent Raman spectroscopy which typically allow chemical imaging of a single resonant vibrational mode of a sample. Here, we utilize a single ultrafast laser source to obtain broadband coherent Raman spectra on a microscope, together with other nonlinear microscopy approaches on the same instrument. We demonstrate that the coherent Raman modality allows broadband measurement (>1000 cm-1), with high spectral resolution (<5 cm-1), with a rapid spectral acquisition rate (3-12 kHz). This enables Raman hyperspectral imaging of > kilo-pixel images at >11 frames per second.

physics.optics↗

arXiv2020

Adaptive dynamic range shift (ADRIFT) quantitative phase imaging

Quantitative phase imaging (QPI) is often used for label-free single cell analysis with its high-contrast images of optical phase delay (OPD) map. Contrary to other imaging methods, sensitivity improvement has not been intensively explored because conventional QPI is sensitive enough to see surface roughness of a substrate which anyway restricts the measurable minimum OPD. However, emerging QPI techniques which utilize, for example, differential image analysis of consecutive temporal frames, such as mid-infrared photothermal QPI, mitigate the minimum OPD limit by decoupling the static OPD contribution and allow to measure much smaller OPD. Here, we propose and demonstrate super-sensitive QPI with expanded dynamic range. It is enabled by adaptive dynamic range shift with combination of wavefront shaping and dark-field QPI techniques. As a proof-of-concept demonstration, we show dynamic range expansion (sensitivity improvement) of QPI by a factor of 6.6 and its utility for improving sensitivity of mid-infrared photothermal QPI. This technique can also be applied for wide-field scattering imaging of dynamically changing nanoscale objects inside and outside a biological cell without losing global cellular morphological image information.

physics.optics↗

arXiv2020

Enhanced spectral resolution for broadband coherent anti-Stokes Raman spectroscopy

The spectral resolution of broadband Fourier-transform coherent anti-Stokes Raman spectroscopy is limited by the maximum optical path length difference that can be scanned within a short time in an interferometer. However, alternatives to the Fourier-transform exist which can bypass this limitation with certain assumptions. We apply one such approach to broadband coherent Raman spectroscopy using interferometers with short delay line (low Fourier spectral resolution) and large delay line (high Fourier spectral resolution). With this method, we demonstrate broadband coherent Raman spectroscopy of closely spaced vibrational bands is possible using a short delay line interferometer, with superior spectral resolution to the longer delay line instrument. We discuss how this approach may be particularly useful for more complex Raman spectra, such as those measured from biological samples.

physics.optics↗

arXiv2019

Label-free biochemical quantitative phase imaging with mid-infrared photothermal effect

Label-free optical imaging is valuable in biology and medicine with its non-destructive property and reduced optical and chemical damages. Quantitative phase (QPI) and molecular vibrational imaging (MVI) are the two most successful label-free methods, providing morphology and biochemistry, respectively, that have pioneered numerous applications along their independent technological maturity over the past few decades. However, the distinct label-free contrasts are inherently complementary and difficult to integrate due to the use of different light-matter interactions. Here, we present a unified imaging scheme that realizes simultaneous and in-situ acquisition of MV-fingerprint contrasts of single cells in the framework of QPI utilizing the mid-infrared photothermal effect. The fully label-free and robust integration of subcellular morphology and biochemistry would have important implications, especially for studying complex and fragile biological phenomena such as drug delivery, cellular diseases and stem cell development, where long-time observation of unperturbed cells are needed under low phototoxicity.

physics.bio-ph↗

arXiv2019

Complementary Vibrational Spectroscopy

Vibrational spectroscopy, comprised of infrared absorption and Raman scattering spectroscopy, is widely used for label-free optical sensing and imaging in various scientific and industrial fields. The group theory states that the two molecular spectroscopy methods are sensitive to vibrations categorized in different point groups and provide complementary vibrational spectra. Therefore, complete vibrational information cannot be acquired by a single spectroscopic device, which has impeded the full potential of vibrational spectroscopy. Here, we demonstrate simultaneous infrared absorption and Raman scattering spectroscopy that allows us to measure the complete broadband vibrational spectra in the molecular fingerprint region with a single instrument based on an ultrashort pulsed laser. The system is based on dual-modal Fourier-transform spectroscopy enabled by efficient use of nonlinear optical effects. Our proof-of-concept experiment demonstrates rapid, broadband and high spectral resolution measurements of complementary spectra of organic liquids for precise and accurate molecular analysis.

physics.chem-ph↗

arXiv2019

Quantitative phase imaging with molecular vibrational sensitivity

Quantitative phase imaging (QPI) quantifies the sample-specific optical-phase-delay enabling objective studies of optically-transparent specimens such as biological samples, but lacks chemical sensitivity limiting its application to morphology-based diagnosis. We present wide-field molecular-vibrational microscopy realized in the framework of QPI utilizing mid-infrared photothermal effect. Our technique provides mid-infrared spectroscopic performance comparable to that of a conventional infrared spectrometer in the molecular fingerprint region of 1,450 - 1,600 cm-1 and realizes wide-field molecular imaging of silica-polystyrene beads mixture over 100 μm x 100 μm area at 1 frame per second with the spatial resolution of 430 nm and 2 - 3 orders of magnitude lower fluence of ~10 pJ/μm2 compared to other high-speed label-free molecular imaging methods, reducing photodamages to the sample. With a high-energy mid-infrared pulse source, our technique could enable high-speed, label-free, simultaneous and in-situ acquisition of quantitative morphology and molecular-vibrational contrast, providing new insights for studies of optically-transparent complex dynamics.

physics.optics↗

arXiv2018

Molecular contrast on phase-contrast microscope

An optical microscope enables image-based findings and diagnosis on microscopic targets, which is indispensable in many scientific, industrial and medical settings. Majority of microscope users are accustomed to standard benchtop microscopes, but it fails to give molecular contrast of the specimen which otherwise requires expensive specialized instruments to measure, accompanied by chemical or optical damages to the sample and/or slow imaging speed. Here, we report on a simple optical instrument, comprising of a semiconductor amplitude-modulated mid-infrared quantum cascade laser, that is attached to a standard microscope to deliver the additional molecular contrast of the specimen on top of its conventional microscopic image. We attach this instrument, termed molecular-contrast unit, to a standard phase-contrast microscope, and demonstrate high-speed label-free molecular-contrast phase-contrast imaging of biological cells under low-power optical illumination. Our simple molecular-contrast unit can empower existing standard microscopes of various users, by delivering a convenient accessibility to the molecular world.

physics.optics↗

arXiv2018

Phase-controlled Fourier-transform spectroscopy

Fourier-transform spectroscopy (FTS) has been widely used as a standard analytical technique over the past half-century. FTS is a simple and robust autocorrelation-based technique that is compatible with both temporally coherent and incoherent light sources, which functions as an active or passive spectrometer. However, this technique has been mostly used for static measurements due to the low scan rate imposed by technological restrictions. This has impeded its application to continuous rapid measurements, which would be of significant interest for a variety of fields, especially when monitoring of non-repeating/transient complex dynamics is desirable. Here, we demonstrate highly efficient FTS operating at a high spectral acquisition rate with a simple delay line based on a dynamic phase-control technique. The independent adjustability of phase and group delays allows us to achieve the Nyquist-limited spectral acquisition rate over 10,000 spectra per second, while maintaining a large spectral bandwidth and high resolution. In addition, we demonstrate the ability of this passive spectrometer working with an incoherent light source.

physics.ins-det↗

arXiv2015

A bidirectional dual-comb ring laser for simple and robust dual-comb spectroscopy

Fourier-transform spectroscopy is an indispensable tool for analyzing chemical samples in scientific research as well as chemical and pharmaceutical industries. Recently, its measurement speed, sensitivity, and precision have been shown to be significantly enhanced by using dual frequency combs. However, wide acceptance of this technique is hindered by its requirement for two frequency combs and active stabilization of the combs. Here we overcome this predicament with a Kerr-lens mode-locked bidirectional ring laser that generates two frequency combs with slightly different pulse repetition rates and a tunable yet highly stable rate difference. This peculiar lasing principle builds on a slight difference in optical cavity length between two counter-propagating lasing modes due to Kerr lensing. Since these combs are produced by the one and same laser cavity, their relative coherence stays passively stable without the need for active stabilization. To show its utility, we demonstrate broadband dual-comb spectroscopy with the single laser.

physics.optics↗

arXiv2014

An octave spanning mid-infrared frequency comb generated in a silicon nanophotonic wire waveguide

We demonstrate an octave-spanning frequency comb with a spectrum covering wavelengths from 1,540 nm up to 3,200 nm. The supercontinuum is generated by pumping a 1-cm long dispersion engineered silicon wire waveguide by 70 fs pulses with an energy of merely 15 pJ. We confirm the phase coherence of the output spectrum by beating the supercontinuum with narrow bandwidth CW lasers. We show that the experimental results are in agreement with numerical simulations.

physics.optics↗

arXiv2014

Few-cycle, Broadband, Mid-infrared Optical Parametric Oscillator Pumped by a 20-fs Ti:sapphire Laser

We report a few-cycle, broadband, singly-resonant optical parametric oscillator (OPO) for the mid-infrared based on MgO-doped periodically-poled LiNbO3 (MgO:PPLN), synchronously pumped by a 20-fs Ti:sapphire laser. By using crystal interaction lengths as short as 250 um, and careful dispersion management of input pump pulses and the OPO resonator, near-transform-limited, few-cycle idler pulses tunable across the mid-infrared have been generated, with as few as 3.7 optical cycles at 2682 nm. The OPO can be continuously tuned over 2179-3732 nm by cavity delay tuning, providing up to 33 mW of output power at 3723 nm. The idler spectra exhibit stable broadband profiles with bandwidths spaning over 422 nm (FWHM) recorded at 3732 nm. We investigate the effect of crystal length on spectral bandwidth and pulse duration at a fixed wavelength, confirming near-transform-limited idler pulses for all grating interaction lengths. By locking the repetition frequency of the pump laser to a radio-frequency reference, and without active stabilization of the OPO cavity length, an idler power stability better than 1.6% rms over >2.75 hours is obtained when operating at maximum output power, in excellent spatial beam quality with TEM00 mode profile.

physics.optics↗

arXiv2014

Differential femtosecond coherent Stokes and anti-Stokes Raman spectroscopy

We demonstrate a novel technique of coherent Raman spectroscopy with a femtosecond laser. We apply to a molecular sample a sequence of pairs of ultrashort excitation and probe pulses, with a linearly increasing time delay between the two pulses from one pair to the next. We measure, as a function of the delay, the intensity modulation in the signal resulting from the differential detection of the Stokes and anti-Stokes radiations generated at the sample. The Fourier transform of such time-domain signal reveals the spectrum of the excited vibrational Raman transitions. The experimental proof-of-principle demonstrates high resolution, broad spectral span and suppression of the non-resonant background, as well as sensitivity enhancement due to the differential detection.

physics.optics↗

arXiv2013

Broadband high-resolution two-photon spectroscopy with laser frequency combs

Two-photon excitation spectroscopy with broad spectral span is demonstrated at Doppler-limited resolution. We describe first Fourier transform two-photon spectroscopy of an atomic sample with two mode-locked laser oscillators in a dual-comb technique. Each transition is uniquely identified by the modulation imparted by the interfering comb excitations. The temporal modulation of the spontaneous two-photon fluorescence is monitored with a single photodetector, and the spectrum is revealed by a Fourier transform.

physics.optics↗