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Kärtner, Franz X.

Publications and source records attributed to Kärtner, Franz X..

Near-complete extraction of maximum stored energy from large-core fibers using coherent pulse stacking amplification of femtosecond pulses

High field science relies on ultrashort pulse lasers with multi-joule pulse energies for studying light–matter interactions under extreme conditions and for driving particle accelerators and secondary radiation sources of x rays, gamma rays, neutrons, positrons, muons, and protons. Next-generation laser drivers will require a 10 3 -10 4 times increase in pulse repetition rates, producing multi-joule energies at multi-kilowatt average powers to enable practical applications in nuclear engineering, advanced materials, medicine, biology, homeland security, and high-energy physics. Spatially coherently combined femtosecond fiber lasers are recognized as a pathway to these next-generation drivers, with significant practical advantages including high efficiency and the possibility of compact integration. However, chirped pulse amplification in fibers is capable of extracting only a small fraction (usually ~1%) of the maximum stored energy. Here we demonstrate near-complete maximum stored energy extraction with low accumulated nonlinearity from a large-core fiber amplifier using coherent pulse stacking amplification. We have amplified a 81-pulse stacking burst in a 85 µm core chirally coupled core Yb-doped fiber, extracting up to 9.5 mJ (~90% of stored energy) with < 4.5 radians of accumulated nonlinear phase, temporally combined this burst into a single pulse, and achieved 4.2 mJ pulses of 313 fs bandwidth-limited duration after compression. This represents, to our knowledge, the highest energy extracted and compressed into a femtosecond pulse from a single fiber amplifier, enabling approximately two orders of magnitude size reduction of future high-energy coherently spatially combined fiber laser arrays.

47 OTHER INSTRUMENTATION↗

Fiber-amplifier-pumped, 1-MHz, 1-µJ, 21-µm, femtosecond OPA with chirped-pulse DFG front-end

High-repetition-rate, high-power, few-cycle mid-infrared lasers with carrier-envelope phase (CEP) stabilization are ideal driving sources for studying strong-field nonlinear processes, such as strong-field driven electron emission, solid-state high-harmonic generation, and nonlinear microscopy. Here, we report on a 1-MHz, 1-μJ, femtosecond, 2.1-µm optical parametric amplifier (OPA), pumped by a Yb-doped fiber chirped-pulse amplifier (CPA) and seeded by a chirped-pulse difference-frequency generation (DFG) front-end providing positively chirped 2.1-μm signal pulses. The home-built multi-stage 1030-nm Yb-doped fiber CPA pump laser generates >55-μJ near-transform-limited (245-fs) pulses at 1 MHz repetition rate using a novel 4-pass all-fiber stretcher/front-end for careful dispersion/spectral management. The chirped-pulse DFG scheme is achieved by wave-mixing the 1030 nm pump pulse with a dispersive wave at 645–735 nm generated in a photonic crystal fiber, allowing passive CEP stability of the 2.1-µm pulses. The 2.1-μm pulse is amplified to 1 μJ in a two-stage dispersion-managed optical parametric amplifier (OPA) with a pump energy of ~21 μJ resulting in 95-fs pulses with nice beam profile without additional pulse compression. Multi-μJ, sub-30 fs pulses can be obtained at full pump energy and additional dispersion compensation. The fiber-amplifier-based mid-infrared OPA can be directly applied to high-harmonic generation in solids and optical-field-driven nanophotonic devices and is a compact front-end for a future high-power, high-repetition-rate, long wavelengths CEP-stabilized source for gas-phase high-order harmonic generation.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Mapping Photoemission and Hot-Electron Emission from Plasmonic Nanoantennas

Understanding plasmon-mediated electron emission and energy transfer on the nanometer length scale is critical to controlling light–matter interactions at nanoscale dimensions. In a high-resolution lithographic material, electron emission and energy transfer lead to chemical transformations. Here, we employ such chemical transformations in two different high-resolution electron-beam lithography resists, poly(methyl methacrylate) (PMMA) and hydrogen silsesquioxane (HSQ), to map local electron emission and energy transfer with nanometer resolution from plasmonic nanoantennas excited by femtosecond laser pulses. We observe exposure of the electron-beam resists (both PMMA and HSQ) in regions on the surface of nanoantennas where the local field is significantly enhanced. Exposure in these regions is consistent with previously reported optical-field-controlled electron emission from plasmonic hotspots as well as earlier work on low-electron-energy scanning probe lithography. For HSQ, in addition to exposure in hotspots, we observe resist exposure at the centers of rod-shaped nanoantennas in addition to exposure in plasmonic hotspots. Optical field enhancement is minimized at the center of nanorods suggesting that exposure in these regions involves a different mechanism to that in plasmonic hotspots. Our simulations suggest that exposure at the center of nanorods results from the emission of hot electrons produced via plasmon decay in the nanorods. Our results provide a means to map both optical-field-controlled electron emission and hot-electron transfer from nanoparticles via chemical transformations produced locally in lithographic materials.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Terahertz-driven linear electron acceleration

The cost, size and availability of electron accelerators are dominated by the achievable accelerating gradient. Conventional high-brightness radio-frequency accelerating structures operate with 30–50 MeVm -1 gradients. Electron accelerators driven with optical or infrared sources have demonstrated accelerating gradients orders of magnitude above that achievable with conventional radio-frequency structures. However, laser-driven wakefield accelerators require intense femtosecond sources and direct laser-driven accelerators suffer from low bunch charge, sub-micron tolerances and sub-femtosecond timing requirements due to the short wavelength of operation. Here we demonstrate linear acceleration of electrons with keV energy gain using optically generated terahertz pulses. Terahertz-driven accelerating structures enable high-gradient electron/proton accelerators with simple accelerating structures, high repetition rates and significant charge per bunch. As a result, these ultra-compact terahertz accelerators with extremely short electron bunches hold great potential to have a transformative impact for free electron lasers, linear colliders, ultrafast electron diffraction, X-ray science and medical therapy with X-rays and electron beams.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗