arXiv subjects

Christoph Gruber

Publications and source records attributed to Christoph Gruber.

4 recordsLinked to original sources

arXiv2025

NIR/VIS dual-comb spectroscopy comparing high and low repetition rate regimes

Dual-comb spectroscopy enables broadband analysis of key molecules with unparalleled frequency resolution and exceptional signal-to-noise ratios across various spectral regions. However, fully harnessing its potential for broadband spectroscopy with high sensitivity and spectral resolution depends critically on selecting the appropriate frequency combs with optimized (comb) parameters tailored to specific applications. This study compares dual-comb spectroscopy systems operating at 80 MHz and 1 GHz repetition rates, in the near infrared and visible spectral regions. The 80 MHz system provides high spectral resolution, ideal for resolving complex spectra, showcased with measurements of NH$_3$ vibrational bands and I$_2$ hyperfine transitions. Utilizing phase-locked feed-forward stabilization, the system delivers excellent signal-to-noise ratios but faces limitations in temporal resolution. The free-running 1 GHz system offers superior temporal resolution and compactness, making it suitable for real-time environmental monitoring in laboratory and field settings. A self-correction algorithm advances the high mutual coherence, enabling high-signal-to-noise measurements without additional electronics. With its 1 GHz resolution, it excels in monitoring NH$_3$ transitions or NO$_2$ lines at high speeds. This work highlights the complementary strengths of these systems for high-resolution spectroscopy and real time trace gas sensing.

physics.optics↗

arXiv2025

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↗

arXiv2020

Nonradiative Energy Transfer between Thickness-Controlled Halide Perovskite Nanoplatelets

Despite showing great promise for optoelectronics, the commercialization of halide perovskite nanostructure-based devices is hampered by inefficient electrical excitation and strong exciton binding energies. While transport of excitons in an energy-tailored system via Förster resonance energy transfer (FRET) could be an efficient alternative, halide ion migration makes the realization of cascaded structures difficult. Here, we show how these could be obtained by exploiting the pronounced quantum confinement effect in two dimensional CsPbBr3 based nanoplatelets (NPls). In thin films of NPls of two predetermined thicknesses, we observe an enhanced acceptor photoluminescence (PL) emission and a decreased donor PL lifetime. This indicates a FRET-mediated process, benefitted by the structural parameters of the NPls. We determine corresponding transfer rates up to k_FRET=0.99 ns^-1 and efficiencies of nearly η_FRET=70%. We also show FRET to occur between perovskite NPls of other thicknesses. Consequently, this strategy could lead to tailored, energy cascade nanostructures for improved optoelectronic devices.

cond-mat.mes-hall↗

arXiv2015

The electronic and magnetic structure of p-element (C,N) doped rutile-TiO$_{2}$; A hybrid DFT study

We study the electronic and magnetic structure of carbon and nitrogen impurities and interstitials in rutile TiO${_2}$. To this end we perform \textit{ab-initio} calculations of a 48-atom supercell employing the VASP code. In order to obtain a realistic description of the electronic and magnetic structure, exchange and correlation are treated with the HSE06 hybrid functional. Both, atomic positions and cell dimensions are fully relaxed. Substitutional carbon and nitrogen are found to have a magnetic moment of 2 and 1$μ{_B}$, respectively, with a tendency for anti-ferromagnetic long range order. For C/N on interstitial sites we find that carbon is non-magnetic while nitrogen always possesses a magnetic moment of 1$μ{_B}$. We find that these interstitial positions are on a saddle point of the total energy. The stable configuration is reached when both carbon and nitrogen form a C-O and N-O dimer with a bond length close to the double bond for CO and NO. This result is in agreement with earlier experimental investigations detecting such N-O entities from XPS measurements. The frequencies of the symmetric stretching mode are calculated for these dimers, which could provide a means for experimental verification. For all configurations investigated both C and N states are found inside the TiO${_2}$ gap. These new electronic states are discussed with respect to tuning doped TiO${_2}$ for the application in photocatalysis

cond-mat.mtrl-sci↗