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Venkata Ramaiah Badarla

Publications and source records attributed to Venkata Ramaiah Badarla.

9 recordsLinked to original sources

Label-free mid-infrared photothermal microscopy revisits intracellular thermal dynamics: what do fluorescent nanothermometers measure?

Fluorescent nanothermometry has revealed pronounced intracellular temperature heterogeneity, establishing the field of single-cell thermal biology. However, these observations have sparked a controversy known as the "10^5 gap issue", because heat conduction calculations in aqueous environments predict that such large temperature distributions cannot be sustained within cells. Here, we address this issue using label-free mid-infrared photothermal microscopy. This technique quantifies heat-induced temperature changes under local thermal equilibrium (LTE), in accordance with the conventional thermodynamic and statistical-mechanical definition of temperature, by detecting refractive index variations. From transient thermal decay measurements, we determined that intracellular thermal diffusivity corresponds to 93-94% that of water. This result indicates that intracellular heat conduction is essentially water-like and rules out the hypothesis that anomalously slow intracellular heat conduction underlies the 10^5 gap discrepancy. We then directly compared fluorescent nanothermometry with our label-free thermometry. Under seconds-long heating, the label-free method exhibited a rapid temperature response consistent with water-like heat conduction. In contrast, fluorescent nanothermometers showed not only a similarly fast response but also an additional slow variation that was absent in the label-free readout. This slow component cannot be explained by temperature changes defined under LTE, but instead likely reflects slower intracellular processes not governed by conductive heat transfer. These results suggest that the "10^5 gap issue" stems from comparing two fundamentally distinct physical quantities: the LTE-defined temperature and a slowly-varying, long-lived non-conductive signal detected by fluorescent nanothermometers.

physics.bio-ph↗

Mid-infrared wide-field nanoscopy

Mid-infrared (MIR) spectroscopy is widely recognized as a powerful, non-distractive method for chemical analysis. However, its utility is constrained by a micrometer-scale spatial resolution imposed by the long-wavelength MIR diffraction limit. This limitation has been recently overcome by MIR photothermal (MIP) imaging, which detects photothermal effects induced in the vicinity of MIR absorbers using a visible-light microscope. Despite its promise, the full potential of its spatial resolving power has not been realized. Here, we present an optimal implementation of wide-field MIP imaging to achieve high spatial resolution. This is accomplished by employing single-objective synthetic-aperture quantitative phase imaging (SOSA-QPI) with synchronized sub-nanosecond MIR and visible light sources, effectively suppressing the resolution-degradation effect caused by photothermal heat diffusion. We demonstrate far-field MIR spectroscopic imaging with a spatial resolution limited by the visible diffraction, down to 125 nm, in the MIR region of 3.12-3.85 um (2,600-3,200 cm-1). This technique, through the use of a shorter visible wavelength and/or a higher objective numerical aperture, holds the potential to achieve a spatial resolution of less than 100 nm, thus paving the way for MIR wide-field nanoscopy.

physics.optics↗

Upconversion time-stretch infrared spectroscopy

High-speed measurement confronts the extreme speed limit when the signal becomes comparable to the noise level. In the context of broadband mid-infrared spectroscopy, state-of-the-art ultrafast Fourier-transform infrared spectrometers, in particular dual-comb spectrometers, have improved the measurement rate up to a few Mspectra/s, which is limited by the signal-to-noise ratio. Time-stretch infrared spectroscopy, an emerging ultrafast frequency-swept mid-infrared spectroscopy technique, has shown a record-high rate of 80 Mspectra/s with an intrinsically higher signal-to-noise ratio than Fourier-transform spectroscopy by more than the square-root of the number of spectral elements. However, it can measure no more than ~30 spectral elements with a low resolution of several cm-1. Here, we significantly increase the measurable number of spectral elements to more than 1,000 by incorporating a nonlinear upconversion process. The one-to-one mapping of a broadband spectrum from the mid-infrared to the near-infrared telecommunication region enables low-loss time-stretching with a single-mode optical fiber and low-noise signal detection with a high-bandwidth photoreceiver. We demonstrate high-resolution mid-infrared spectroscopy of gas-phase methane molecules with a high resolution of 0.017 cm-1. This unprecedentedly high-speed vibrational spectroscopy technique would satisfy various unmet needs in experimental molecular science, e.g., measuring ultrafast dynamics of irreversible phenomena, statistically analyzing a large amount of heterogeneous spectral data, or taking broadband hyperspectral images at a high frame rate.

physics.optics↗

Mid-infrared photothermal single-live-cell imaging beyond video rate

Advancement in mid-infrared (MIR) technology has led to promising biomedical applications of MIR spectroscopy, such as liquid biopsy or breath diagnosis. On the contrary, MIR microscopy has been rarely used for live biological samples in an aqueous environment due to the lack of spatial resolution and the large water absorption background. Recently, mid-infrared photothermal (MIP) imaging has proven to be applicable to 2D and 3D single-cell imaging with high spatial resolution inherited from visible light. However, the maximum measurement rate has been limited to several frames/s, limiting its range of use. Here, we develop a significantly-improved wide-field MIP quantitative phase microscope with two orders-of-magnitude higher signal-to-noise ratio than previous MIP imaging techniques and demonstrate single-live-cell imaging beyond video rate. We first derive optimal system design by numerically simulating thermal conduction following the photothermal effect. Then, we develop the designed system with a homemade nanosecond MIR optical parametric oscillator and a high full-well-capacity image sensor. Our high-speed and high-spatial-resolution MIR microscope has great potential to become a new tool for life science, in particular for single-live-cell analysis.

physics.optics↗

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↗

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↗

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↗

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↗

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↗