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Spectroscopy|25 Article(s)
Enhanced terahertz vibrational absorption spectroscopy using an integrated high-Q resonator
Zhibo Hou, Liao Chen, Rongwu Liu, Chi Zhang, Xiaojun Wu, and Xinliang Zhang
The terahertz (THz) absorption spectrum is a powerful method to identify substances. The improvement focuses on sensitivity and recovery ability. Here, we demonstrate enhanced THz vibrational absorption spectroscopy based on an on-chip THz whispering gallery mode resonator (THz-WGMR). A THz-WGMR with high Q can store energy and enhance the interaction between the THz waves and the target substances to capture the unique absorption fingerprint information. Therefore, it possesses significant sensitivity to identify trace amounts of substances. As a proof of concept, lactose powder and glucose powder are applied to demonstrate the effectiveness of our approach in recovering fingerprint absorption spectroscopy. Compared with a straight waveguide, the high sensitivity of the THz-WGMR is illustrated. The change of the transmissivity caused by the lactose reaches 7.8 dB around 532 GHz for the THz-WGMR, while only 1.4 dB for the straight waveguide, demonstrating the state-of-the-art sensing performance in fingerprint absorption recovery. We believe the proposed integrated THz-WGMR will promote the THz identification of tiny fingerprint substances. The terahertz (THz) absorption spectrum is a powerful method to identify substances. The improvement focuses on sensitivity and recovery ability. Here, we demonstrate enhanced THz vibrational absorption spectroscopy based on an on-chip THz whispering gallery mode resonator (THz-WGMR). A THz-WGMR with high Q can store energy and enhance the interaction between the THz waves and the target substances to capture the unique absorption fingerprint information. Therefore, it possesses significant sensitivity to identify trace amounts of substances. As a proof of concept, lactose powder and glucose powder are applied to demonstrate the effectiveness of our approach in recovering fingerprint absorption spectroscopy. Compared with a straight waveguide, the high sensitivity of the THz-WGMR is illustrated. The change of the transmissivity caused by the lactose reaches 7.8 dB around 532 GHz for the THz-WGMR, while only 1.4 dB for the straight waveguide, demonstrating the state-of-the-art sensing performance in fingerprint absorption recovery. We believe the proposed integrated THz-WGMR will promote the THz identification of tiny fingerprint substances.
Photonics Research
- Publication Date: Jul. 01, 2024
- Vol. 12, Issue 7, 1542 (2024)
Instantaneous preparation of gold-carbon dot nanocomposites for on-site SERS identification of pathogens in diverse interfaces
Yanxian Guo, Ye Liu, Chaocai Luo, Yue Zhang, Yang Li, Fei Zhou, Zhouyi Guo, Zhengfei Zhuang, and Zhiming Liu
Rapid detection of pathogens present on contaminated surfaces is crucial for food safety and public health due to the high morbidity and mortality of bacterial infections. Herein, a sensitive and efficient method for on-site identification of foodborne pathogens on anisotropic surfaces was developed by using an in situ instantaneously prepared surface-enhanced Raman scattering (SERS) platform. To achieve this, molybdenum-doped gallic acid-derived carbon dots (MCDs) are utilized as the reductant for synthesizing Au@MCDs nanohybrids within just 3 s at ambient temperature. The synergistic effect of the electromagnetic enhancement and charge transfer of Au@MCDs enables excellent SERS performance 10 times stronger than bare Au NPs. The bioassay platform requires less than 5 min to complete the quantitative detection of foodborne pathogens on various microbial-contaminated interfaces with a sensitivity of 10 CFU/mL. This innovative strategy breaks the long-standing limitations of SERS substrates in practical use, such as the time-consuming process, interference of residual surfactants, poor surface stability, and few application scenarios, providing a promising tool for widespread applications in biomedical research and clinical diagnostics. Rapid detection of pathogens present on contaminated surfaces is crucial for food safety and public health due to the high morbidity and mortality of bacterial infections. Herein, a sensitive and efficient method for on-site identification of foodborne pathogens on anisotropic surfaces was developed by using an in situ instantaneously prepared surface-enhanced Raman scattering (SERS) platform. To achieve this, molybdenum-doped gallic acid-derived carbon dots (MCDs) are utilized as the reductant for synthesizing Au@MCDs nanohybrids within just 3 s at ambient temperature. The synergistic effect of the electromagnetic enhancement and charge transfer of Au@MCDs enables excellent SERS performance 10 times stronger than bare Au NPs. The bioassay platform requires less than 5 min to complete the quantitative detection of foodborne pathogens on various microbial-contaminated interfaces with a sensitivity of 10 CFU/mL. This innovative strategy breaks the long-standing limitations of SERS substrates in practical use, such as the time-consuming process, interference of residual surfactants, poor surface stability, and few application scenarios, providing a promising tool for widespread applications in biomedical research and clinical diagnostics.
Photonics Research
- Publication Date: May. 31, 2024
- Vol. 12, Issue 6, 1303 (2024)
High-speed impulsive stimulated Brillouin microscopy|Spotlight on Optics
Jiarui Li, Taoran Le, Hongyuan Zhang, Haoyun Wei, and Yan Li
Brillouin microscopy, which maps the elastic modulus from the frequency shift of scattered light, has evolved to a faster speed for the investigation of rapid biomechanical changes. Impulsive stimulated Brillouin scattering (ISBS) spectroscopy has the potential to speed up measurement through the resonant amplification interaction from pulsed excitation and time-domain continuous detection. However, significant progress has not been achieved due to the limitation in signal-to-noise ratio (SNR) and the corresponding need for excessive averaging to maintain high spectral precision. Moreover, the limited spatial resolution also hinders its application in mechanical imaging. Here, by scrutinizing the SNR model, we design a high-speed ISBS microscope through multi-parameter optimization including phase, reference power, and acquisition time. Leveraging this, with the further assistance of the Matrix Pencil method for data processing, three-dimensional mechanical images are mapped under multiple contrast mechanisms for a millimeter-scale polydimethylsiloxane pattern immersed in methanol, enabling the identification of these two transparent materials without any contact or labeling. Our experimental results demonstrate the capability to maintain high spectral precision and resolution at a sub-millisecond integration time for one pixel. With a two-order improvement in the speed and a tenfold improvement in the spatial resolution over the state-of-the-art systems, this method makes it possible for ISBS microscopes to sensitively investigate rapid mechanical changes in time and space. Brillouin microscopy, which maps the elastic modulus from the frequency shift of scattered light, has evolved to a faster speed for the investigation of rapid biomechanical changes. Impulsive stimulated Brillouin scattering (ISBS) spectroscopy has the potential to speed up measurement through the resonant amplification interaction from pulsed excitation and time-domain continuous detection. However, significant progress has not been achieved due to the limitation in signal-to-noise ratio (SNR) and the corresponding need for excessive averaging to maintain high spectral precision. Moreover, the limited spatial resolution also hinders its application in mechanical imaging. Here, by scrutinizing the SNR model, we design a high-speed ISBS microscope through multi-parameter optimization including phase, reference power, and acquisition time. Leveraging this, with the further assistance of the Matrix Pencil method for data processing, three-dimensional mechanical images are mapped under multiple contrast mechanisms for a millimeter-scale polydimethylsiloxane pattern immersed in methanol, enabling the identification of these two transparent materials without any contact or labeling. Our experimental results demonstrate the capability to maintain high spectral precision and resolution at a sub-millisecond integration time for one pixel. With a two-order improvement in the speed and a tenfold improvement in the spatial resolution over the state-of-the-art systems, this method makes it possible for ISBS microscopes to sensitively investigate rapid mechanical changes in time and space.
Photonics Research
- Publication Date: Mar. 25, 2024
- Vol. 12, Issue 4, 730 (2024)
Frequency-comb-linearized, widely tunable lasers for coherent ranging
Baoqi Shi, Yi-Han Luo, Wei Sun, Yue Hu, Jinbao Long, Xue Bai, Anting Wang, and Junqiu Liu
Tunable lasers, with the ability to continuously vary their emission wavelengths, have found widespread applications across various fields such as biomedical imaging, coherent ranging, optical communications, and spectroscopy. In these applications, a wide chirp range is advantageous for large spectral coverage and high frequency resolution. Besides, the frequency accuracy and precision also depend critically on the chirp linearity of the laser. While extensive efforts have been made on the development of many kinds of frequency-agile, widely tunable, narrow-linewidth lasers, wideband yet precise methods to characterize and linearize laser chirp dynamics are also demanded. Here we present an approach to characterize laser chirp dynamics using an optical frequency comb. The instantaneous laser frequency is tracked over terahertz bandwidth at 1 MHz intervals. Using this approach we calibrate the chirp performance of 12 tunable lasers from Toptica, Santec, New Focus, EXFO, and NKT that are commonly used in fiber optics and integrated photonics. In addition, with acquired knowledge of laser chirp dynamics, we demonstrate a simple frequency-linearization scheme that enables coherent ranging without any optical or electronic linearization unit. Our approach not only presents novel wideband, high-resolution laser spectroscopy, but is also critical for sensing applications with ever-increasing requirements on performance. Tunable lasers, with the ability to continuously vary their emission wavelengths, have found widespread applications across various fields such as biomedical imaging, coherent ranging, optical communications, and spectroscopy. In these applications, a wide chirp range is advantageous for large spectral coverage and high frequency resolution. Besides, the frequency accuracy and precision also depend critically on the chirp linearity of the laser. While extensive efforts have been made on the development of many kinds of frequency-agile, widely tunable, narrow-linewidth lasers, wideband yet precise methods to characterize and linearize laser chirp dynamics are also demanded. Here we present an approach to characterize laser chirp dynamics using an optical frequency comb. The instantaneous laser frequency is tracked over terahertz bandwidth at 1 MHz intervals. Using this approach we calibrate the chirp performance of 12 tunable lasers from Toptica, Santec, New Focus, EXFO, and NKT that are commonly used in fiber optics and integrated photonics. In addition, with acquired knowledge of laser chirp dynamics, we demonstrate a simple frequency-linearization scheme that enables coherent ranging without any optical or electronic linearization unit. Our approach not only presents novel wideband, high-resolution laser spectroscopy, but is also critical for sensing applications with ever-increasing requirements on performance.
Photonics Research
- Publication Date: Mar. 18, 2024
- Vol. 12, Issue 4, 663 (2024)
Precision determination of dipole transition elements with a single ion
H. Shao, Y.-B. Tang, H.-L. Yue, F.-F. Wu, Z.-X. Ma, Y. Huang, L.-Y. Tang, H. Guan, and K.-L. Gao
In the field of quantum metrology, transition matrix elements are crucial for accurately evaluating the black-body radiation shift of the clock transition and the amplitude of the related parity-violating transition, and can be used as probes to test quantum electrodynamic effects, especially at the 10-3–10-4 level. We developed a universal experimental approach to precisely determine the dipole transition matrix elements by using the shelving technique, for the species where two transition channels are involved, in which the excitation pulses with increasing duration were utilized to induce shelving, and the resulting shelving probabilities were determined by counting the scattered photons from the excited P1/22 state to the S1/22 ground state. Using the scattered photons offers several advantages, including insensitivity to fluctuations in magnetic field, laser intensity, and frequency detuning. An intensity-alternating sequence to minimize detection noise and a real-time approach for background photon correction were implemented in parallel. We applied this technique to a single Yb+ ion, and determined the 6p P1/22-5d D23/2 transition matrix element 2.9979(20) ea0, which indicates an order of magnitude improvement over existing reports. By combining our result with the 6p P1/22 lifetime of 8.12(2) ns, we extracted the 6s S1/22-6p P1/22 transition matrix element to be 2.4703(31) ea0. The accurately determined dipole transition matrix elements can serve as a benchmark for the development of high-precision atomic many-body theoretical methods. In the field of quantum metrology, transition matrix elements are crucial for accurately evaluating the black-body radiation shift of the clock transition and the amplitude of the related parity-violating transition, and can be used as probes to test quantum electrodynamic effects, especially at the 10-3–10-4 level. We developed a universal experimental approach to precisely determine the dipole transition matrix elements by using the shelving technique, for the species where two transition channels are involved, in which the excitation pulses with increasing duration were utilized to induce shelving, and the resulting shelving probabilities were determined by counting the scattered photons from the excited P1/22 state to the S1/22 ground state. Using the scattered photons offers several advantages, including insensitivity to fluctuations in magnetic field, laser intensity, and frequency detuning. An intensity-alternating sequence to minimize detection noise and a real-time approach for background photon correction were implemented in parallel. We applied this technique to a single Yb+ ion, and determined the 6p P1/22-5d D23/2 transition matrix element 2.9979(20) ea0, which indicates an order of magnitude improvement over existing reports. By combining our result with the 6p P1/22 lifetime of 8.12(2) ns, we extracted the 6s S1/22-6p P1/22 transition matrix element to be 2.4703(31) ea0. The accurately determined dipole transition matrix elements can serve as a benchmark for the development of high-precision atomic many-body theoretical methods.
Photonics Research
- Publication Date: Sep. 30, 2024
- Vol. 12, Issue 10, 2242 (2024)
Dual-comb spectroscopy from the ultraviolet to mid-infrared region based on high-order harmonic generation
Yuanfeng Di, Zhong Zuo, Daowang Peng, Daping Luo, Chenglin Gu, and Wenxue Li
Dual-comb spectroscopy (DCS) has revolutionized numerous spectroscopic applications due to its high spectral resolution and fast measurement speed. Substantial efforts have been made to obtain a coherent dual-comb source at various spectral regions through nonlinear frequency conversion, where the preservation of coherence has become a problem of great importance. In this study, we report the generation of coherent dual-comb sources covering from the ultraviolet to mid-infrared region based on high-order harmonic generation. Driven by high-repetition-rate femtosecond mid-infrared dual-comb pump pulses, up to ninth-order harmonic was generated from the ultraviolet to mid-infrared region using an aperiodically poled lithium niobate waveguide. To investigate the coherence property of the high-order harmonic generation, DCS was performed at every generated spectral region from 450 to 3600 nm. The measured dual-comb spectra with distinctive tooth-resolved structures show the well-preserved coherence without apparent degradation after the cascaded quadratic nonlinear processes. The subsequent methane absorption spectroscopy at multiple spectral regions of different harmonics was carried out to characterize the spectroscopic capability of the system. These results demonstrate the potential of our scheme to generate compact and coherent broadband optical frequency combs for simultaneous multi-target detections. Dual-comb spectroscopy (DCS) has revolutionized numerous spectroscopic applications due to its high spectral resolution and fast measurement speed. Substantial efforts have been made to obtain a coherent dual-comb source at various spectral regions through nonlinear frequency conversion, where the preservation of coherence has become a problem of great importance. In this study, we report the generation of coherent dual-comb sources covering from the ultraviolet to mid-infrared region based on high-order harmonic generation. Driven by high-repetition-rate femtosecond mid-infrared dual-comb pump pulses, up to ninth-order harmonic was generated from the ultraviolet to mid-infrared region using an aperiodically poled lithium niobate waveguide. To investigate the coherence property of the high-order harmonic generation, DCS was performed at every generated spectral region from 450 to 3600 nm. The measured dual-comb spectra with distinctive tooth-resolved structures show the well-preserved coherence without apparent degradation after the cascaded quadratic nonlinear processes. The subsequent methane absorption spectroscopy at multiple spectral regions of different harmonics was carried out to characterize the spectroscopic capability of the system. These results demonstrate the potential of our scheme to generate compact and coherent broadband optical frequency combs for simultaneous multi-target detections.
Photonics Research
- Publication Date: Jun. 30, 2023
- Vol. 11, Issue 7, 1373 (2023)
Recent advances on applications of NV− magnetometry in condensed matter physics
Ying Xu, Weiye Zhang, and Chuanshan Tian
Measuring magnetic response from spin and current is of fundamental interest in condensed matter physics. Negatively charged nitrogen-vacancy (NV-) centers in diamond are emerging as a robust and versatile quantum sensor owing to their high sensitivity, nanometer-scale spatial resolution, and noninvasive operation with access to static and dynamic magnetic and electron transport properties. In this review, we discuss the rapidly growing interest in the implementation of NV- magnetometry to explore condensed matter physics, focusing on three topics: anti/ferromagnetic materials, superconductors, and metals/semimetals/semiconductors. Measuring magnetic response from spin and current is of fundamental interest in condensed matter physics. Negatively charged nitrogen-vacancy (NV-) centers in diamond are emerging as a robust and versatile quantum sensor owing to their high sensitivity, nanometer-scale spatial resolution, and noninvasive operation with access to static and dynamic magnetic and electron transport properties. In this review, we discuss the rapidly growing interest in the implementation of NV- magnetometry to explore condensed matter physics, focusing on three topics: anti/ferromagnetic materials, superconductors, and metals/semimetals/semiconductors.
Photonics Research
- Publication Date: Feb. 27, 2023
- Vol. 11, Issue 3, 393 (2023)
Interpulse stimulation Fourier-transform coherent anti-Stokes Raman spectroscopy
Minjian Lu, Yujia Zhang, Xinyi Chen, Yan Li, and Haoyun Wei
Exploiting the time-resolving ability of ultrafast pulses, Fourier-transform coherent anti-Stokes Raman scattering (FT-CARS) stands out among the coherent Raman spectroscopic techniques for providing high-speed vibrational spectra with high spectral resolution, high Raman intensity, and immunity to nonresonant background. However, the impulsive stimulation nature of FT-CARS imposes heavy demands on the laser source and makes it inherently difficult to monitor high-frequency vibrations. Here, a novel FT-CARS strategy to our knowledge based on interpulse stimulation is proposed to provide more flexible measuring wavenumber region and lighten the requirement on ultrafast pulses. The mechanism of this technique is analyzed theoretically, and simulation is performed to show an orders-of-magnitude improvement of Raman intensity in the high-wavenumber region by the method. Experimentally, an ytterbium-doped fiber laser and photonic crystal fiber-based solitons are employed to provide two ∼100-fs pulses as the pump and Stokes, respectively, and to perform interpulse stimulation FT-CARS without sophisticated dispersion control devices. The high-wavenumber region and upper-part fingerprint region measurements are demonstrated as examples of flexible measurement. Combined with other rapid scanning techniques, such as resonant scanners or a dual-comb scheme, this interpulse stimulation FT-CARS promises to make the fascinating FT-CARS available for any desired wavenumber region, covering many more realistic scenarios for biomedical, pathological, and environmental research. Exploiting the time-resolving ability of ultrafast pulses, Fourier-transform coherent anti-Stokes Raman scattering (FT-CARS) stands out among the coherent Raman spectroscopic techniques for providing high-speed vibrational spectra with high spectral resolution, high Raman intensity, and immunity to nonresonant background. However, the impulsive stimulation nature of FT-CARS imposes heavy demands on the laser source and makes it inherently difficult to monitor high-frequency vibrations. Here, a novel FT-CARS strategy to our knowledge based on interpulse stimulation is proposed to provide more flexible measuring wavenumber region and lighten the requirement on ultrafast pulses. The mechanism of this technique is analyzed theoretically, and simulation is performed to show an orders-of-magnitude improvement of Raman intensity in the high-wavenumber region by the method. Experimentally, an ytterbium-doped fiber laser and photonic crystal fiber-based solitons are employed to provide two ∼100-fs pulses as the pump and Stokes, respectively, and to perform interpulse stimulation FT-CARS without sophisticated dispersion control devices. The high-wavenumber region and upper-part fingerprint region measurements are demonstrated as examples of flexible measurement. Combined with other rapid scanning techniques, such as resonant scanners or a dual-comb scheme, this interpulse stimulation FT-CARS promises to make the fascinating FT-CARS available for any desired wavenumber region, covering many more realistic scenarios for biomedical, pathological, and environmental research.
Photonics Research
- Publication Date: Feb. 01, 2023
- Vol. 11, Issue 2, 357 (2023)
Gas sensing with 7-decade dynamic range by laser vector spectroscopy combining absorption and dispersion
Xiutao Lou, Yue Wang, Ning Xu, and Yongkang Dong
Laser absorption spectroscopy (LAS) has been widely used for unambiguous detection and accurate quantification of gas species in a diverse range of fields. However, up-to-date LAS-based gas sensors still face challenges in applications where gas concentrations change in a wide range, since it is extremely difficult to balance spectral analysis strategies for different optical thicknesses. Here we present laser vector spectroscopy that combines absorption spectroscopy with dispersion spectroscopy, simultaneously taking advantage of the former’s high sensitivity in the low-concentration region and the latter’s high linearity in the high-concentration region. In the proof-of-concept demonstration of acetylene measurement, it achieves a linear dynamic range of 6×107 (R2>0.9999), which surpasses all other state-of-the-art LAS techniques by more than an order of magnitude, with the capability of highly accurate quantification retained. The proposed laser spectroscopic method paves a novel way of developing large-dynamic-range gas sensors for environmental, medical, and industrial applications. Laser absorption spectroscopy (LAS) has been widely used for unambiguous detection and accurate quantification of gas species in a diverse range of fields. However, up-to-date LAS-based gas sensors still face challenges in applications where gas concentrations change in a wide range, since it is extremely difficult to balance spectral analysis strategies for different optical thicknesses. Here we present laser vector spectroscopy that combines absorption spectroscopy with dispersion spectroscopy, simultaneously taking advantage of the former’s high sensitivity in the low-concentration region and the latter’s high linearity in the high-concentration region. In the proof-of-concept demonstration of acetylene measurement, it achieves a linear dynamic range of 6×107 (R2>0.9999), which surpasses all other state-of-the-art LAS techniques by more than an order of magnitude, with the capability of highly accurate quantification retained. The proposed laser spectroscopic method paves a novel way of developing large-dynamic-range gas sensors for environmental, medical, and industrial applications.
Photonics Research
- Publication Date: Sep. 27, 2023
- Vol. 11, Issue 10, 1687 (2023)
Lamb-dip saturated-absorption cavity ring-down rovibrational molecular spectroscopy in the near-infrared
Roberto Aiello, Valentina Di Sarno, Maria Giulia Delli Santi, Maurizio De Rosa, Iolanda Ricciardi, Giovanni Giusfredi, Paolo De Natale, Luigi Santamaria, and Pasquale Maddaloni
The high-detection-sensitivity saturated-absorption cavity ring-down (SCAR) technique is extended to Lamb-dip spectroscopy of rovibrational molecular transitions in the near-infrared region. Frequency-comb-referenced sub-Doppler saturation measurements, performed on the acetylene (ν1+ν3+ν4←ν4) R(14)e line at 6562 cm-1, are analyzed by a SCAR global line profile fitting routine, based on a specially developed theoretical model. Compared to a conventional cavity ring-down evaluation, our approach yields dip profiles with a linewidth freed from saturation broadening effects, reduced by 40%, and a signal-to-noise ratio increased by 90%. Ultimately, an overall (statistical and systematic) fractional uncertainty as low as 7×10-12 is achieved for the absolute line-center frequency. At the same time, our method is also able to accurately infer the linear (non-saturated) behavior of the gas absorption, providing Lamb-dip-based line strength measurements with a relative uncertainty of 0.5%. The high-detection-sensitivity saturated-absorption cavity ring-down (SCAR) technique is extended to Lamb-dip spectroscopy of rovibrational molecular transitions in the near-infrared region. Frequency-comb-referenced sub-Doppler saturation measurements, performed on the acetylene (ν1+ν3+ν4←ν4) R(14)e line at 6562 cm-1, are analyzed by a SCAR global line profile fitting routine, based on a specially developed theoretical model. Compared to a conventional cavity ring-down evaluation, our approach yields dip profiles with a linewidth freed from saturation broadening effects, reduced by 40%, and a signal-to-noise ratio increased by 90%. Ultimately, an overall (statistical and systematic) fractional uncertainty as low as 7×10-12 is achieved for the absolute line-center frequency. At the same time, our method is also able to accurately infer the linear (non-saturated) behavior of the gas absorption, providing Lamb-dip-based line strength measurements with a relative uncertainty of 0.5%.
Photonics Research
- Publication Date: Jul. 13, 2022
- Vol. 10, Issue 8, 1803 (2022)
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