arXiv subjects

Henry Timmers

Publications and source records attributed to Henry Timmers.

15 recordsLinked to original sources

arXiv2020

Fully phase-stabilized 1 GHz turnkey frequency comb at 1.56 $μ$m

Low noise and high repetition rate optical frequency combs are desirable for many applications from timekeeping to precision spectroscopy. For example, gigahertz repetition rate sources greatly increase the acquisition speed of spectra in a dual-comb modality when compared to lower repetition rate sources, while still maintaining sufficient instantaneous resolution to resolve ro-vibrational signatures from molecules in a variety of conditions. In this paper, we present the stabilization and characterization of a turnkey commercial 1~GHz mode-locked laser that operates at telecom wavelengths (1.56 $μ$m). Fiber amplification and spectral broadening result in the high signal-to-noise ratio detection and stabilization of $\textit{f}_{\textit{ceo}}$ with 438 mrad of residual phase noise (integrated from 10$^2$ to 10$^7$ Hz). Simultaneously, we stabilize the beatnote between the nearest comb mode and a cavity stabilized continuous-wave laser at 1.55 $μ$m with 41 mrad of residual phase noise (integrated from 10$^2$ to 10$^7$ Hz). This robust, self-referenced comb system is built with off-the-shelf polarization-maintaining fiber components and will be useful for a wide range of low noise frequency comb applications that benefit from the increased repetition rate.

physics.optics↗

arXiv2020

A six-octave optical frequency comb from a scalable few-cycle erbium fiber laser

A compact and robust coherent laser light source that provides spectral coverage from the ultraviolet to infrared is desirable for numerous applications, including heterodyne super resolution imaging[1], broadband infrared microscopy[2], protein structure determination[3], and standoff atmospheric trace-gas detection[4]. Addressing these demanding measurement problems, laser frequency combs[5] combine user-defined spectral resolution with sub-femtosecond timing and waveform control to enable new modalities of high-resolution, high-speed, and broadband spectroscopy[6-9]. In this Letter we introduce a scalable source of near-single-cycle, 0.56 MW pulses generated from robust and low-noise erbium fiber (Er:fiber) technology, and we use it to generate a frequency comb that spans six octaves from the ultraviolet (350 nm) to mid-infrared (22500 nm). The high peak power allows us to exploit the second-order nonlinearities in infrared-transparent, nonlinear crystals (LiNbO$_3$, GaSe, and CSP) to provide a robust source of phase-stable infrared ultra-short pulses with simultaneous spectral brightness exceeding that of an infrared synchrotron[10]. Additional cascaded second-order nonlinearities in LiNbO$_3$ lead to comb generation with four octaves of simultaneous coverage (0.350 to 5.6 $μ$m). With a comb-tooth linewidth of 10 kHz at 193 THz, we realize a notable spectral resolving power exceeding 10$^{10}$ across 0.86 PHz of bandwidth. We anticipate that this compact and accessible technology will open new opportunities for multi-band precision spectroscopy, coherent microscopy, ultra-high sensitivity nanoscopy, astronomical spectroscopy, and precision carrier-envelope phase (CEP) stable strong field phenomena.

physics.optics↗

arXiv2020

Mid-infrared frequency combs at 10 GHz

We demonstrate mid-infrared (MIR) frequency combs at 10 GHz repetition rate via intra-pulse difference-frequency generation (DFG) in quasi-phase-matched nonlinear media. Few-cycle pump pulses ($\mathbf{\lesssim}$15 fs, 100 pJ) from a near-infrared (NIR) electro-optic frequency comb are provided via nonlinear soliton-like compression in photonic-chip silicon-nitride waveguides. Subsequent intra-pulse DFG in periodically-poled lithium niobate waveguides yields MIR frequency combs in the 3.1--4.1 $μ$m region, while orientation-patterned gallium phosphide provides coverage across 7--11 $μ$m. Cascaded second-order nonlinearities simultaneously provide access to the carrier-envelope-offset frequency of the pump source via in-line f-2f nonlinear interferometry. The high-repetition rate MIR frequency combs introduced here can be used for condensed phase spectroscopy and applications such as laser heterodyne radiometry.

physics.optics↗

arXiv2019

Mid-infrared frequency comb with 6.7 W average power based on difference frequency generation

We report on the development of a high-power mid-infrared frequency comb with 100 MHz repetition rate and 100 fs pulse duration. Difference frequency generation is realized between two branches derived from an Er:fiber comb, amplified separately in Yb:fiber and Er:fiber amplifiers. Average powers of 6.7 W and 14.9 W are generated in the 2.9 $μ$m idler and 1.6 $μ$m signal, respectively. With high average power, excellent beam quality, and passive carrier-envelope phase stabilization, this light source is a promising platform for generating broadband frequency combs in the far infrared, visible, and deep ultraviolet.

physics.optics↗

arXiv2019

Nonlinear silicon waveguides generating broadband, spectrally engineered frequency combs spanning 2.0-8.5 um

Nanophotonic waveguides with sub-wavelength mode confinement and engineered dispersion profiles are an excellent platform for application-tailored nonlinear optical interactions at low pulse energies. Here, we present fully air clad suspended-silicon waveguides for infrared frequency comb generation with optical bandwidth limited only by the silicon transparency. The achieved spectra are lithographically tailored to span 2.1 octaves in the mid-infrared (2.0-8.5 um or 1170--5000 cm-1) when pumped at 3.10 um with 100 pJ pulses. Novel fork-shaped couplers provide efficient input coupling with only 1.5 dB loss. The coherence, brightness, and the stability of the generated light are highlighted in a dual frequency comb setup in which individual comb-lines are resolved with 30 dB extinction ratio and 100 MHz spacing in the wavelength range of 4.8-8.5 um (2100-1170 cm-1). These sources are used for broadband gas- and liquid-phase dual-comb spectroscopy with 100 MHz comb-line resolution. We achieve a peak spectral signal-to-noise ratio of 10 Hz^0.5 across a simultaneous bandwidth containing 112,200 comb-lines. These results provide a pathway to further integration with the developing high repetition rate frequency comb lasers for compact sensors with applications in chip-based chemical analysis and spectroscopy.

physics.optics↗

arXiv2018

$χ^{(2)}$ mid-infrared frequency comb generation and stabilization with few-cycle pulses

Mid-infrared laser frequency combs are compelling sources for precise and sensitive metrology with applications in molecular spectroscopy and spectro-imaging. The infrared atmospheric window between 3-5.5 $μ$m in particular provides vital information regarding molecular composition. Using a robust, fiber-optic source of few-cycle pulses in the near-infrared, we experimentally demonstrate ultra-broad bandwidth nonlinear phenomena including harmonic and difference frequency generation in a single pass through periodically poled lithium niobate (PPLN). These $χ^{(2)}$ nonlinear optical processes result in the generation of frequency combs across the mid-infrared atmospheric window which we employ for dual-comb spectroscopy of acetone and carbonyl sulfide with resolution as high as 0.003 cm$^{-1}$. Moreover, cascaded $χ^{(2)}$ nonlinearities in the same PPLN directly provide the carrier-envelope offset frequency of the near-infrared driving pulse train in a compact geometry.

physics.optics↗

arXiv2018

Infrared electric-field sampled frequency comb spectroscopy

Molecular spectroscopy in the mid-infrared portion of the electromagnetic spectrum (3--25 um) has been a cornerstone interdisciplinary analytical technique widely adapted across the biological, chemical, and physical sciences. Applications range from understanding mesoscale trends in climate science via atmospheric monitoring to microscopic investigations of cellular biological systems via protein characterization. Here, we present a compact and comprehensive approach to infrared spectroscopy incorporating the development of broadband laser frequency combs across 3--27 um, encompassing the entire mid-infrared, and direct electric-field measurement of the corresponding near single-cycle infrared pulses of light. Utilizing this unified apparatus for high-resolution and accurate frequency comb spectroscopy, we present the infrared spectra of important atmospheric compounds such as ammonia and carbon dioxide in the molecular fingerprint region. To further highlight the ability to study complex biological systems, we present a broadband spectrum of a monoclonal antibody reference material consisting of more than 20,000 atoms. The absorption signature resolves the amide I and II vibrations, providing a means to study secondary structures of proteins. The approach described here, operating at the boundary of ultrafast physics and precision spectroscopy, provides a table-top solution and a widely adaptable technique impacting both applied and fundamental scientific studies.

physics.ins-det↗

arXiv2018

Tunable mid-infrared generation via wide-band four wave mixing in silicon nitride waveguides

We experimentally demonstrate wide-band (>100 THz) frequency down-conversion of near-infrared (NIR) femtosecond-scale pulses from an Er:fiber laser to the mid-infrared (MIR) using four-wave-mixing (FWM) in photonic-chip silicon-nitride waveguides. The engineered dispersion in the nanophotonic geometry, along with the wide transparency range of silicon nitride, enables large-detuning FWM phase-matching and results in tunable MIR from 2.6-3.6 um on a single chip with 100-pJ-scale pump-pulse energies. Additionally, we observe > 20 dB broadband parametric gain for the NIR pulses when the FWM process is operated in a frequency up-conversion configuration. Our results demonstrate how integrated photonic circuits could realize multiple nonlinear optical phenomena on the same chip and lead to engineered synthesis of broadband, tunable, and coherent light across the NIR and MIR wavelength bands from fiber-based pumps.

physics.app-ph↗

arXiv2018

Mid-infrared frequency comb generation via cascaded quadratic nonlinearities in quasi-phase-matched waveguides

We experimentally demonstrate a simple configuration for mid-infrared (MIR) frequency comb generation in quasi-phase-matched lithium niobate waveguides using the cascaded-$χ^{(2)}$ nonlinearity. With nanojoule-scale pulses from an Er:fiber laser, we observe octave-spanning supercontinuum in the near-infrared with dispersive-wave generation in the 2.5--3 $\textμ$m region and intra-pulse difference-frequency generation in the 4--5 $\textμ$m region. By engineering the quasi-phase-matched grating profiles, tunable, narrow-band MIR and broadband MIR spectra are both observed in this geometry. Finally, we perform numerical modeling using a nonlinear envelope equation, which shows good quantitative agreement with the experiment---and can be used to inform waveguide designs to tailor the MIR frequency combs. Our results identify a path to a simple single-branch approach to mid-infrared frequency comb generation in a compact platform using commercial Er:fiber technology.

physics.optics↗

arXiv2017

Dual frequency comb spectroscopy in the molecular fingerprint region

Spectroscopy in the molecular fingerprint spectral region (6.5-20 $μ$m) yields critical information on material structure for physical, chemical and biological sciences. Despite decades of interest and effort, this portion of the electromagnetic spectrum remains challenging to cover with conventional laser technologies. In this report, we present a simple and robust method for generating super-octave, optical frequency combs in the fingerprint region through intra-pulse difference frequency generation in an orientation-patterned gallium phosphide crystal. We demonstrate the utility of this unique coherent light source for high-precision, dual-comb spectroscopy in methanol and ethanol vapor. These results highlight the potential of laser frequency combs for a wide range of molecular sensing applications, from basic molecular spectroscopy to nanoscopic imaging.

physics.optics↗

arXiv2017

High-harmonic generation in periodically poled waveguides

Optical waveguides made from periodically poled materials provide high confinement of light and enable the generation of new wavelengths via quasi-phase-matching, making them a key platform for nonlinear optics and photonics. However, such devices are not typically employed for high-harmonic generation. Here, using 200-fs, 10-nJ-level pulses of 4100 nm light at 1 MHz, we generate high harmonics up to the 13th harmonic (315 nm) in a chirped, periodically poled lithium niobate (PPLN) waveguide. Total conversion efficiencies into the visible--ultraviolet region are as high as 10 percent. We find that the output spectrum depends on the waveguide poling period, indicating that quasi-phase-matching plays a significant role. In the future, such periodically poled waveguides may enable compact sources of ultrashort pulses at high repetition rates and provide new methods of probing the electronic structure of solid-state materials.

physics.optics↗

arXiv2017

Versatile silicon-waveguide supercontinuum for coherent mid-infrared spectroscopy

Infrared spectroscopy is a powerful tool for basic and applied science. The molecular spectral fingerprints in the 3 um to 20 um region provide a means to uniquely identify molecular structure for fundamental spectroscopy, atmospheric chemistry, trace and hazardous gas detection, and biological microscopy. Driven by such applications, the development of low-noise, coherent laser sources with broad, tunable coverage is a topic of great interest. Laser frequency combs possess a unique combination of precisely defined spectral lines and broad bandwidth that can enable the above-mentioned applications. Here, we leverage robust fabrication and geometrical dispersion engineering of silicon nanophotonic waveguides for coherent frequency comb generation spanning 70 THz in the mid-infrared (2.5 um to 6.2 um). Precise waveguide fabrication provides significant spectral broadening and engineered spectra targeted at specific mid-infrared bands. We use this coherent light source for dual-comb spectroscopy at 5 um.

physics.optics↗

arXiv2015

Attosecond Quantum-Beat Spectroscopy in Helium

The evolution of electron wavepackets determines the course of many physical and chemical phenomena and attosecond spectroscopy aims to measure and control such dynamics in real-time. Here, we investigate radial electron wavepacket motion in Helium by using an XUV attosecond pulse train to prepare a coherent superposition of excited states and a delayed femtosecond IR pulse to ionize them. Quantum beat signals observed in the high resolution photoelectron spectrogram allow us to follow the field-free evolution of the bound electron wavepacket and determine the time-dependent ionization dynamics of the low-lying 2p state.

physics.atom-ph↗

arXiv2012

Ultrafast dynamics of neutral superexcited Oxygen: A direct measurement of the competition between autoionization and predissociation

Using ultrafast extreme ultraviolet pulses, we performed a direct measurement of the relaxation dynamics of neutral superexcited states corresponding to the nlσ_g(c^4Σ_u^-) Rydberg series of O_2. An XUV attosecond pulse train was used to create a temporally localized Rydberg wavepacket and the ensuing electronic and nuclear dynamics were probed using a time-delayed femtosecond near-infrared pulse. We investigated the competing predissociation and autoionization mechanisms for superexcited molecules and found that autoionization is dominant for the low n Rydberg states. We measured an autoionization lifetime of 92+/-6 fs and 180+/-10 fs for (5s,4d)σ_g and (6s,5d)σ_g Rydberg state groups respectively. We determine that the disputed neutral dissociation lifetime for the ν=0 vibrational level of the Rydberg series is 1100+/-100fs.

physics.chem-ph↗

arXiv2011

Real-time evolution of a laser-dressed Helium atom: Attosecond-resolved two-color photoionization study

Using extreme-ultraviolet attosecond-pulse-trains, we investigate the photoionization dynamics of a Helium atom in the presence of moderately-strong (~10^12 W/cm^2) femtosecond laser pulses. The electronic structure of a laser-dressed atom is traced in real-time through precision measurements of ion-yields and photo-electron angular distributions. Quantum interferences between photo-excitation paths are interpreted using the Floquet formalism. As the laser pulse intensity ramps on femtosecond timescales, we observe transitions between ionization channels mediated by different atomic resonances. The quantum phase of interfering paths is extracted for each channel and compared with simulations. Our results elucidate photoionization mechanisms in strong-fields and open the doors for photo-absorption/ionization control schemes.

physics.atom-ph↗