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1. Raman spectrometer for high precision temperature sensing of atmospheric gases

   https://doi.org/10.1364/AO.419882  

   Mashburn, Carter ; Borysow, Jacek ( March 2021 , Applied Optics)

   We present a highly accurate Raman spectrometer capable of measuring changes in atmospheric temperature as small as 0.75 K with high spatial and temporal resolution. The spectrometer is based on a laser diode tuned to the resonant absorption line of the${}^{85}\mathrm{R}\mathrm{b}$isotope near 780.0 nm. A heated glass cell containing Rb atoms was used as an ultranarrowband atomic absorption notch filter with$0.3\mathrm{c}{\mathrm{m}}^{-<\#comment/>1}$bandwidth and optical density as high as four. This filter was placed in front of the spectrograph and blocked up to 99.99% of the elastically scattered laser light, which made it possible to resolve the pure-rotational Raman spectra of molecular atmospheric gases. The relative intensities of pure-rotational Raman transitions were then used to infer atmospheric temperature changes.

    

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2. Terahertz nonlinear index extraction via full-phase analysis

   https://doi.org/10.1364/OL.399999  

   Garriga Francis, Kareem J. ; Lim Pac Chong, Mervin ; E, Yiwen ; Zhang, X. -C. ( October 2020 , Optics Letters)

   We experimentally show the spectrally averaged nonlinear refractive index and absorption coefficient for liquid water, water vapor,$\mathrm{\alpha <\#comment/>}$-pinene, and Si using a full-phase analysis in the terahertz regime through a standard time-domain spectrometer. Our results confirm that the nonlinear index of refraction of the liquid samples in this regime exceeds the near-infrared optical nonlinear index by six orders of magnitude. In the case of liquid water and water vapor at atmospheric pressure, we find a nonlinear index of$7.8\times <\#comment/>{10}^{-<\#comment/>10}{\mathrm{c}\mathrm{m}}^2/\mathrm{W}$and$6\times <\#comment/>{10}^{-<\#comment/>11}{\mathrm{c}\mathrm{m}}^2/\mathrm{W}$, respectively, which are both much larger than expected.

    

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3. Mid-IR spectroscopy of Er 3+ doped low-phonon CsCdCl 3 and CsPbCl 3 crystals

   https://doi.org/10.1364/JOSAB.470152  

   Brown, Ei Ei ; Fleischman, Zackery D. ; McKay, Jason ; Hommerich, Uwe ; Kabir, Al Amin ; Riggins, Jazmine ; Trivedi, Sudhir ; Dubinskii, Mark ( September 2022 , Journal of the Optical Society of America B)

   The mid-IR spectroscopic properties of${\mathrm{E}\mathrm{r}}^{3+}$doped low-phonon${\mathrm{C}\mathrm{s}\mathrm{C}\mathrm{d}\mathrm{C}\mathrm{l}}_3$and${\mathrm{C}\mathrm{s}\mathrm{P}\mathrm{b}\mathrm{C}\mathrm{l}}_3$crystals grown by the Bridgman technique have been investigated. Using optical excitations at$\sim <\#comment/>800\mathrm{n}\mathrm{m}$and$\sim <\#comment/>660\mathrm{n}\mathrm{m}$, both crystals exhibited IR emissions at$\sim <\#comment/>1.55$,$\sim <\#comment/>2.75$,$\sim <\#comment/>3.5$, and$\sim <\#comment/>4.5\text{µ<\#comment/>}\mathrm{m}$at room temperature. The mid-IR emission at 4.5 µm, originating from the${}^4{\mathrm{I}}_{9/2}\to <\#comment/>{}^4{\mathrm{I}}_{11/2}$transition, showed a long emission lifetime of$\sim <\#comment/>11.6\mathrm{m}\mathrm{s}$for${\mathrm{E}\mathrm{r}}^{3+}$doped${\mathrm{C}\mathrm{s}\mathrm{C}\mathrm{d}\mathrm{C}\mathrm{l}}_3$, whereas${\mathrm{E}\mathrm{r}}^{3+}$doped${\mathrm{C}\mathrm{s}\mathrm{P}\mathrm{b}\mathrm{C}\mathrm{l}}_3$exhibited a shorter lifetime of$\sim <\#comment/>1.8\mathrm{m}\mathrm{s}$. The measured emission lifetimes of the${}^4{\mathrm{I}}_{9/2}$state were nearly independent of the temperature, indicating a negligibly small nonradiative decay rate through multiphonon relaxation, as predicted by the energy-gap law for low-maximum-phonon energy hosts. The room temperature stimulated emission cross sections for the${}^4{\mathrm{I}}_{9/2}\to <\#comment/>{}^4{\mathrm{I}}_{11/2}$transition in${\mathrm{E}\mathrm{r}}^{3+}$doped${\mathrm{C}\mathrm{s}\mathrm{C}\mathrm{d}\mathrm{C}\mathrm{l}}_3$and${\mathrm{C}\mathrm{s}\mathrm{P}\mathrm{b}\mathrm{C}\mathrm{l}}_3$were determined to be$\sim <\#comment/>0.14\times <\#comment/>{10}^{-<\#comment/>20}{\mathrm{c}\mathrm{m}}^2$and$\sim <\#comment/>0.41\times <\#comment/>{10}^{-<\#comment/>20}{\mathrm{c}\mathrm{m}}^2$, respectively. The results of Judd–Ofelt analysis are presented and discussed.

    

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4. Electro-optic interface for ultrasensitive intracavity electric field measurements at microwave and terahertz frequencies

   https://doi.org/10.1364/OPTICA.384160  

   Benea-Chelmus, Ileana-Cristina ; Salamin, Yannick ; Settembrini, Francesca Fabiana ; Fedoryshyn, Yuriy ; Heni, Wolfgang ; Elder, Delwin L. ; Dalton, Larry R. ; Leuthold, Juerg ; Faist, Jérôme ( May 2020 , Optica)

   Electro-optic quantum coherent interfaces map the amplitude and phase of a quantum signal directly to the phase or intensity of a probe beam. At terahertz frequencies, a fundamental challenge is not only to sense such weak signals (due to a weak coupling with a probe in the near-infrared) but also to resolve them in the time domain. Cavity confinement of both light fields can increase the interaction and achieve strong coupling. Using this approach, current realizations are limited to low microwave frequencies. Alternatively, in bulk crystals, electro-optic sampling was shown to reach quantum-level sensitivity of terahertz waves. Yet, the coupling strength was extremely weak. Here, we propose an on-chip architecture that concomitantly provides subcycle temporal resolution and an extreme sensitivity to sense terahertz intracavity fields below 20 V/m. We use guided femtosecond pulses in the near-infrared and a confinement of the terahertz wave to a volume of$V_{\mathrm{T}\mathrm{H}\mathrm{z}}\sim <\#comment/>{10}^{-<\#comment/>9}({\mathrm{\lambda <\#comment/>}}_{\mathrm{T}\mathrm{H}\mathrm{z}}/2{)}^3$in combination with ultraperformant organic molecules ($r_{33}=170\mathrm{p}\mathrm{m}/\mathrm{V}$) and accomplish a record-high single-photon electro-optic coupling rate of$g_{\mathrm{e}\mathrm{o}}=2\mathrm{\pi <\#comment/>}\times <\#comment/>0.043\mathrm{G}\mathrm{H}\mathrm{z}$, 10,000 times higher than in recent reports of sensing vacuum field fluctuations in bulk media. Via homodyne detection implemented directly on chip, the interaction results into an intensity modulation of the femtosecond pulses. The single-photon cooperativity is$C_0=1.6\times <\#comment/>{10}^{-<\#comment/>8}$, and the multiphoton cooperativity is$C=0.002$at room temperature. We show$><\#comment/>70\mathrm{d}\mathrm{B}$dynamic range in intensity at 500 ms integration under irradiation with a weak coherent terahertz field. Similar devices could be employed in future measurements of quantum states in the terahertz at the standard quantum limit, or for entanglement of subsystems on subcycle temporal scales, such as terahertz and near-infrared quantum bits.

    

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5. Needle-based deep-neural-network camera

   https://doi.org/10.1364/AO.415059  

   Guo, Ruipeng ; Nelson, Soren ; Menon, Rajesh ( March 2021 , Applied Optics)

   We experimentally demonstrate a camera whose primary optic is a cannula/needle ($\mathrm{d}\mathrm{i}\mathrm{a}\mathrm{m}\mathrm{e}\mathrm{t}\mathrm{e}\mathrm{r}=0.22\mathrm{m}\mathrm{m}$and$\mathrm{l}\mathrm{e}\mathrm{n}\mathrm{g}\mathrm{t}\mathrm{h}=12.5\mathrm{m}\mathrm{m}$) that acts as a light pipe transporting light intensity from an object plane (35 cm away) to its opposite end. Deep neural networks (DNNs) are used to reconstruct color and grayscale images with a field of view of 18° and angular resolution of$\sim <\#comment/>{0.4}^{\circ <\#comment/>}$. We showed a large effective demagnification of$127\times <\#comment/>$. Most interestingly, we showed that such a camera could achieve close to diffraction-limited performance with an effective numerical aperture of 0.045, depth of focus$\sim <\#comment/>16\text{µ<\#comment/>}\mathrm{m}$, and resolution close to the sensor pixel size (3.2 µm). When trained on images with depth information, the DNN can create depth maps. Finally, we show DNN-based classification of the EMNIST dataset before and after image reconstructions. The former could be useful for imaging with enhanced privacy.

    

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