96 research outputs found

    Transition of pulsed operation from Q-switching to continuous-wave mode-locking in a Yb:KLuW waveguide laser

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    We report on the diverse pulsed operation regimes of a femtosecond-laser-written Yb:KLuW channel waveguide laser emitting near 1040 nm. By the precise position tuning of a carbon-nanotube-coated saturable absorber (SA) mirror, the transition of the pulsed operation from Q-switching, Q-switched mode-locking and finally sub-GHz continuous-wave mode-locking are obtained based on the interplay of dispersion and mode area control. The Q-switched pulses exhibit typical fast SA Q-switched pulse characteristics depending on absorbed pump powers. In the Q-switched mode-locking, amplitude modulations of the mode-locked pulses on the Q-switched envelope are observed. The radio-frequency spectrum represents the coexistence of Q-switching and mode-locking signals. In the purely mode-locked operation, the waveguide laser generates 2.05-ps pulses at 0.5 GHz.National Research Foundation of Korea (2018H1A2AA1061480, 2019R1A2C3003504, 2020R1A4A2002828); Spanish Government (FIS2017-87970-R, MAT2016-75716-C2-1-R (AEI/FEDER,UE)); Junta de Castilla y León (SA287P18); Generalitat de Catalunya (2017SGR755)

    Optical, vibrational, thermal, electrical, damage and phase-matching properties of lithium thioindate

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    Lithium thioindate (LiInS2_{2}) is a new nonlinear chalcogenide biaxial material transparent from 0.4 to 12 Ό\mum, that has been successfully grown in large sizes and good optical quality. We report on new physical properties that are relevant for laser and nonlinear optics applications. With respect to AgGaS(e)2_2 ternary chalcopyrite materials, LiInS2_{2} displays a nearly-isotropic thermal expansion behavior, a 5-times larger thermal conductivity associated with high optical damage thresholds, and an extremely low intensity-dependent absorption allowing direct high-power downconversion from the near-IR to the deep mid-IR. Continuous-wave difference-frequency generation (5-11Ό \mum) of Ti:sapphire laser sources is reported for the first time.Comment: 27 pages, 21 figures. Replaces the previous preprint (physics/0307082) with the final version as it will be published in J. Opt. Soc. Am. B 21(11) (Nov. 2004 issue

    Inflammatory bowel disease addressed by Caco-2 and monocyte-derived macrophages : an opportunity for an in vitro drug screening assay

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    Infammatory bowel disease (IBD) is a widespread disease, afecting a growing demographic. The treatment of chronic infammation located in the GI-tract is dependent on the severity; therefore, the IBD treatment pyramid is commonly applied. Animal experimentation plays a key role for novel IBD drug development; nevertheless, it is ethically questionable and limited in its throughput. Reliable and valid in vitro assays ofer the opportunity to overcome these limitations. We combined Caco-2 with monocyte-derived macrophages and exposed them to known drugs, targeting an in vitro-in vivo correlation (IVIVC) with a focus on the severity level and its related drug candidate. This co-culture assay addresses namely the intestinal barrier and the immune response in IBD. The drug efcacy was analyzed by an LPS-infammation of the co-culture and drug exposure according to the IBD treatment pyramid. Efcacy was defned as the range between LPS control (0%) and untreated co-culture (100%) independent of the investigated read-out (TEER, Papp, cytokine release: IL-6, IL-8, IL-10, TNF-α). The release of IL-6, IL-8, and TNF-α was identifed as an appropriate readout for a fast drug screening (“yes–no response”). TEER showed a remarkable IVIVC correlation to the human treatment pyramid (5-ASA, Prednisolone, 6-mercaptopurine, and infiximab) with an R2 of 0.68. Similar to the description of an adverse outcome pathway (AOP) framework, we advocate establishing an “Efcacy Outcome Pathways (EOPs)” framework for drug efcacy assays. The in vitro assay ofers an easy and scalable method for IBD drug screening with a focus on human data, which requires further validation

    Femtosecond-laser-written Tm:KLu(WO_4)_2 waveguide lasers

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    Depressed-index channel waveguides with a circular and photonic crystal cladding structures are prepared in a bulk monoclinic Tm:KLu(WO4)2 crystal by 3D direct femtosecond laser writing. The channel waveguide structures are characterized and laser operation is achieved using external mirrors. In the continuous-wave mode, the maximum output power of 46 mW is achieved at 1912 nm corresponding to a slope efficiency of 15.2% and a laser threshold of only 21 mW. Passive -switching of a waveguide with a circular cladding is realized using single-walled carbon nanotubes. Stable 7 nJ/50 ns pulses are achieved at a repetition rate of 1.48 MHz. This first demonstration of ∌2 Όm fs-laser-written waveguide lasers based on monoclinic double tungstates is promising for further lasers of this type doped with Tm3+and Ho3+ ions .Ministerio de EconomĂ­a y Competitividad (MINECO) (FIS2013-44174-P, FIS2015-71933-REDT, MAT2013-47395-C4-4-R, MAT2016-75716-C2-1-R, TEC 2014-55948-R); Departament d’InnovaciĂł, Universitats i Empresa, Generalitat de Catalunya (DIUE) (2014SGR1358); Junta de Castilla y LeĂłn (UIC016, SA046U16); InstituciĂł Catalana de Recerca i Estudis Avançats (ICREA) Academia (2010ICREA-02); H2020 Marie SkƂodowska-Curie Actions (MSCA) (657630); Government of the Russian Federation (074-U01); National Research Foundation of Korea (NRF) Korea of MSIP (2016R1A2A1A05005381)

    Passively Q-switched femtosecond-laser-written thulium waveguide laser based on evanescent field interaction with carbon nanotubes

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    Surface channel waveguides (WGs) were fabricated in a monoclinic Tm3+:KLu(WO4)2 crystal by femtosecond direct laser writing (fs-DLW). The WGs consisted of a half-ring cladding with diameters of 50 and 60 ÎŒm located just beneath the crystal surface. They were characterized by confocal laser microscopy and -Raman spectroscopy, indicating a reduced crystallinity and stress-induced birefringence of the WG cladding. In continuous-wave (CW) mode, under Ti:sapphire laser pumping at 802 nm, the maximum output power reached 171.1 mW at 1847.4 nm, corresponding to a slope efficiency of 37.8% for the 60 ÎŒm diameter WG. The WG propagation loss was 0.7±0.3 dB/cm. The top surface of the WGs was spin-coated by a polymethyl methacrylate film containing randomly oriented (spaghetti-like) arc-discharge single-walled carbon nanotubes serving as a saturable absorber based on evanescent field coupling. Stable passively -switched (PQS) operation was achieved. The PQS 60 ÎŒm diameter WG laser generated a record output power of 150 mW at 1846.8 nm with =34.6%. The conversion efficiency with respect to the CW mode was 87.6%. The best pulse characteristics (energy/duration) were 105.6 nJ/98 ns at a repetition rate of 1.42 MHz.Ministerio de EconomĂ­a y Competitividad (MINECO) (FIS2013-44174-P, FIS2015-71933-REDT, MAT2016-75716-C2-1-R (AEI/FEDER,UE), TEC2014-55948-R); AgĂšncia de GestiĂł d’Ajuts Universitaris i de Recerca (AGAUR) (2017SGR755); ConsejerĂ­a de EducaciĂłn, Junta de Castilla y LeĂłn (SA046U16, UIC016); Generalitat de Catalunya (2016FI_B00844, 2017FI_B100158, 2018 FI_B2 00123)

    Diode-pumped Nd: BaY 2 F 8 picosecond laser mode-locked with carbon nanotube saturable absorbers

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    Picosecond pulse generation near 1-m wavelength has been achieved with a Nd: BaY 2 F 8 (Nd:BaYF) laser mode-locked using a single-walled carbon nanotube saturable absorber (SWCNT-SA). The laser was operated at its main 1049-nm transition, generating 8.5-ps pulses with Ï·70-mW output power for Ï·570-mW absorbed pump power. This is the first demonstration of cw mode-locking in the picosecond regime with Nd-doped crystals and SWCNT-SAs. The requirements on the SWCNT-SA for successful mode-locking in relatively narrowband neodymium lasers are reviewed and their implications are discussed

    High-power few-cycle THz generation at MHz repetition rates in an organic crystal

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    Ultrafast terahertz (THz) spectroscopy is a potent tool for studying the fundamental properties of matter. Limitations of current THz sources, however, preclude the technique being applied in certain advanced configurations or in the measurement of, e.g., strongly absorbing samples. In response to this problem, here we demonstrate the generation of 1.38 mW broadband THz radiation at 10 MHz repetition rate by combining the highly efficient nonlinear organic crystal HMQ-TMS with ultrafast pump pulses generated using a simple and stable external pulse compression of a high power, near-infrared (NIR) femtosecond ytterbium-doped fiber (Yb:fiber) laser. Utilizing spectral broadening in a large core, polarization maintaining photonic crystal fiber and a pair of SF11 prisms, we achieve a tenfold pulse compression of the Yb:fiber laser, yielding compressed 0.35 ”J pulses with a full-width at half maximum pulse duration of 22 fs, exerting a peak power of 13.8 MW at a repetition rate of 10 MHz. THz generation through optical rectification of the NIR pulses is explored in two distinct thicknesses of the organic crystal, leading to a maximum conversion efficiency of ∌5.5 · 10−4, an order of magnitude higher than that achieved with inorganic nonlinear crystals, e.g., gallium phosphide, for similar pump parameters. The focused THz beam has a peak on-axis field strength greater than 6.4 kV cm−1 in unpurged atmosphere. We believe that our moderately strong-field THz source is well suited to a variety of applications in ultrafast THz spectroscopy, in particular THz-enabled scattering-type near-field, and scanning tunneling spectroscopy, where multi-MHz repetition rate sources are required

    Design strategy of highly efficient nonlinear optical orange‐colored crystals with two electron‐withdrawing groups

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    A new class of highly efficient nonlinear optical organic salt crystals is reported. In nonlinear optics based on organic materials, it is well known that using two electron-withdrawing groups (EWGs) onto cationic electron acceptors instead of conventional one EWG remarkably enhances microscopic optical nonlinearity for chromophores. However, the corresponding organic crystals possessing enhanced large macroscopic optical nonlinearity have not been reported yet. Herein, a design strategy is proposed for obtaining highly efficient nonlinear optical crystals based on two EWGs in cationic electron acceptors. Introducing a phenolic electron donor, promoting a head-to-tail interionic assembly, along with a two-EWG N-pyrimidinyl pyridinium electron acceptor in cationic chromophores results in a preferred non-centrosymmetric, perfectly parallel alignment of chromophores in crystal. Newly designed OPR (4-(4-hydroxystyryl)-1-(pyrimidin-2-yl)pyridinium) crystals exhibit approximately two times larger effective first hyperpolarizability than that of analogous N-alkyl OHP (4-(4-hydroxystyryl)-1-methylpyridinium) crystals based on only one EWG. OPR crystals exhibit comparable second-order optical nonlinearity to benchmark red-colored DAST (4-(4-(dimethylamino)styryl)-1-methylpyridinium 4-methylbenzenesulfonate) crystals, but a significant blue-shifted absorption resulting in orange-color crystals. Therefore, phenolic organic salt crystals using two EWGs are highly promising materials for various nonlinear optical applications
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