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Martin Schultze

Publications and source records attributed to Martin Schultze.

7 recordsLinked to original sources

Transmissive extreme ultraviolet metagrating

Extreme ultraviolet (EUV) radiation is a key tool for attosecond physics and lithography. However, strong material absorption limits the availability of transmissive optical elements at these wavelengths. Metaoptics exploit geometry to control the wavefront of transmitted light on the nanoscale and, due to their minimal thickness, promise to fill this gap. Here, we demonstrate the first EUV metaoptics for broadband applications: we design, fabricate, and experimentally investigate a blazed transmissive EUV metagrating and compare it with a focused-ion-beam-milled sawtooth-blazed grating serving as an in-situ reference. The metagrating achieves an angular dispersion of 0.04°/nm with a directionality (the ratio of the +1st and -1st diffraction order efficiency) of up to 5.8. The device shows phase-based operation up to 50 eV photon energy (down to 25 nm vacuum wavelength) and an octave-spanning bandwidth of 25 eV, doubling the previous spectral window addressable by metasurfaces. Comparing both gratings' performance reveals that, when accounting for fabrication constraints, EUV metasurfaces are competitive with free-form optics while offering scalability to large apertures and arbitrary phase profiles. Broadband transmissive operation removes the need for grazing incidence optics, defeating a major source of aberrations, and allows polarization-insensitive spectral analysis, enabling energy-resolved ultrafast spectroscopy in compact experimental configurations.

physics.optics

Roadmap on Attosecond Science

Twenty-five years have passed since the first experimental demonstration of attosecond pulses, marking the advent of our ability to resolve and control electron motion in real time. What began as a technological breakthrough - generating the shortest flashes ever produced - has evolved into a powerful approach for probing and steering electronic dynamics in atoms, molecules, and solids. This roadmap, authored by leading experts in the field, surveys the recent rapid progress in the generation and characterization of attosecond pulses, emerging attosecond measurement and control techniques, and their expanding range of applications. It reviews current and future developments in attosecond light sources, including novel laser technologies, waveform synthesizers, new schemes for high-order harmonic generation, attosecond pulse generation at free-electron lasers, and structured light. Advances in attosecond measurement methodologies are also discussed, encompassing all-attosecond pump-probe spectroscopy, attosecond four-wave mixing, attosecond microscopy, spectroscopy with light transients, and attosecond interferometry. Furthermore, the roadmap addresses applications of attosecond spectroscopy to reveal electron dynamics in molecules and condensed matter systems from both theoretical and experimental perspectives, and highlights emerging directions at the interface with quantum optics and quantum entanglement. Overall, this work aims to serve as a comprehensive resource for navigating the evolving landscape of attosecond science.

physics.optics

Streaming Self-Corrected Dual-Comb Spectrometer

We radically simplify coherently averaged dual-comb spectroscopy by introducing a real-time self-correction system: a radio frequency system-on-chip computes each incoming dual-comb interferogram's phase, frequency, and arrival time; calculates changes in the combs' carrier-envelope offset frequency and repetition rate difference; and immediately phase-corrects the incoming interferogram data stream. The algorithm supports up to 0.3 GHz interferogram frequency bandwidth and thus combines fast measurement times (corresponding to high detunings) with broadband optical detection. Using this system, we achieve comb-resolved spectroscopy with Fourier-limited linewidth, coherent averaging over arbitrarily long durations, and high signal-to-noise ratios (e.g., up to 2900 for 150 s averaging time). Iodine and acetylene spectroscopy yield excellent agreement with literature over an optical bandwidth of 10 THz in the visible and near-infrared. Common dual-comb spectroscopy self-correction requires a bright and continuous interferogram train. We lift this requirement by introducing cross-channel correction: the algorithm measures phase fluctuations from a reference channel and predicts and corrects their influence on a signal channel. This enables correcting unstable or intermittent signals (typical, e.g., in field measurements), or low-amplitude signals with amplified phase fluctuations (relevant for nonlinearly upconverted combs). The approach makes instantaneous dual-comb spectroscopy available to everyday applications.

physics.optics

Ultra-resolution photochemical sensing

Photochemistry in the earth's atmosphere is driven by the sun, continuously altering the concentration and spatial distribution of pollutants. Precisely monitoring their atmospheric abundance relies predominantly on optical sensing, which requires the knowledge of exact absorption cross sections. One key pollutant which impacts many photochemical reaction-pathways is formaldehyde. Agreement on formaldehyde absolute absorption cross section remains elusive in the photochemically-relevant ultraviolet spectral region, hampering sensitive concentration tracking. Here, we introduce free-running ultraviolet dual comb spectroscopy, combining high spectral resolution (1 GHz), broad spectral coverage (12 THz), and fast acquisition speed (500 ms), as a novel method for absolute absorption cross section determination with unprecedented fidelity. Within this bandwidth, our method uncovers almost one order of magnitude more rovibrational transitions than detected before which leads to refined rotational constants for high-level quantum simulations of molecular eigenstates. This ultra-resolution method can be generalized to provide a universal tool for fast electronic fingerprinting of atmospherically-relevant species, both for sensing applications and to benchmark improvements of ab-initio quantum theory.

physics.optics

Combining Brillouin spectroscopy and machine learned interatomic potentials to probe mechanical properties of metal organic frameworks

The mechanical properties of metal-organic frameworks (MOFs) are of high fundamental and also practical relevance. A particularly intriguing technique for determining anisotropic elastic tensors is Brillouin scattering, which so far has rarely been used for highly complex materials like MOFs. In the present contribution, we apply this technique to study a newly synthesized MOF-type material, referred to as GUT2. We show that when combining the experiments with state-of-the-art simulations of elastic properties and phonon bands (based on machine-learned force fields and dispersion-corrected density-functional theory). This provides a comprehensive understanding of the experimental signals, which are correlated with the longitudinal and transverse sound velocities. Moreover, even when dealing with comparably small single crystals, which limit the range of accessible experimental data, combining the insights from simulations and experiments allows the determination of approximate values for the components of the elastic tensor of the studied material.

cond-mat.mtrl-sci

Attosecond state-resolved carrier motion in quantum materials probed by soft X-ray XANES

Recent developments in attosecond technology led to tabletop X-ray spectroscopy in the soft X-ray range, thus uniting the element- and state-specificity of core-level x-ray absorption spectroscopy with the time resolution to follow electronic dynamics in real time. We describe recent work in attosecond technology and investigations into materials such as Si, SiO2, GaN, Al2O3, Ti, TiO2, enabled by the convergence of these two capabilities. We showcase the state-of-the-art on isolated attosecond soft x-ray pulses for x-ray absorption near edge spectroscopy (XANES) to observe the 3d-state dynamics of the semi-metal TiS2 with attosecond resolution at the Ti L-edge (460 eV). We describe how the element- and state-specificity at the transition metal L-edge of the quantum material allows to unambiguously identify how and where the optical field influences charge carriers. This precision elucidates that the Ti:3d conduction band states are efficiently photo-doped to a density of 1.9 x 10^21 cm^-3 and that the light-field induces coherent motion of intra-band carriers across 38% of the first Brillouin zone. Lastly, we describe the prospects with such unambiguous real-time observation of carrier dynamics in specific bonding or anti-bonding states and speculate that such capability will bring unprecedented opportunities towards an engineered approach for designer materials with pre-defined properties and efficiency. Examples are composites of semiconductors and insulators like Si, Ge, SiO2, GaN, BN, quantum materials like graphene, TMDCs, or high-Tc superconductors like NbN or LaBaCuO. Exiting are prospects to scrutinize canonical questions in multi-body physics such as whether the electrons or lattice trigger phase transitions.

cond-mat.mtrl-sci

Petahertz Spintronics

The enigmatic coupling between electronic and magnetic phenomena was one of the riddles propelling the development of modern electromagnetism. Today, the fully controlled electric field evolution of ultrashort laser pulses permits the direct and ultrafast control of electronic properties of matter and is the cornerstone of light-wave electronics. In sharp contrast, because there is no first order interaction between light and spins, the magnetic properties of matter can only be affected indirectly on the much slower tens-of-femtosecond timescale in a sequence of optical excitation followed by the rearrangement of the spin structure. Here we record an orders of magnitude faster magnetic switching with sub-femtosecond response time by initiating optical excitations with near-single-cycle laser pulses in a ferromagnetic layer stack. The unfolding dynamics are tracked in real-time by a novel attosecond time-resolved magnetic circular dichroism (atto-MCD) detection scheme revealing optically induced spin and orbital momentum transfer (OISTR) in synchrony with light field driven charge relocation. In tandem with ab-initio quantum dynamical modelling, we show how this mechanism provides simultaneous control over electronic and magnetic properties that are at the heart of spintronic functionality. This first incarnation of attomagnetism observes light field coherent control of spin-dynamics in the initial non-dissipative temporal regime and paves the way towards coherent spintronic applications with Petahertz clock rates.

physics.app-ph