arXiv subjects

W. G. Schmidt

Publications and source records attributed to W. G. Schmidt.

5 recordsLinked to original sources

arXiv2026

Surface-exciton enhanced SHG response in few-layer 2H-TMDC

We explore the nonlinear optical properties of few-layer MoS2 by means of polarization and laser-power-dependent measurements as well as ab initio techniques. While for even layer samples a weak second-harmonic (SH) signal can be attributed to the presence of surface defects or interface effects, our measurements resolve a layer-number dependent signal for odd-layer samples. For the excitation energy of 780 nm, we find that the SH intensity decreases steadily with the layer number. Our simulations demonstrate that this effect cannot be purely attributed to modifications of the band structure, but requires the inclusion of excitonic effects and can be explained by the increasing delocalization of excitons with increasing sample thickness.

physics.optics↗

arXiv2024

14N Hyperfine and nuclear interactions of axial and basal NV centers in 4H-SiC: A high frequency (94 GHz) ENDOR study

The nitrogen-vacancy (NV) centers (NCVSi) - in 4H silicon carbide (SiC) constitute an ensemble of spin S = 1 solid state qubits interacting with the surrounding 14N and 29Si nuclei. As quantum applications based on a polarization transfer from the electron spin to the nuclei require the knowledge of the electron-nuclear interaction parameters, we have used high-frequency (94 GHz) electron-nuclear double resonance spectroscopy combined with first-principles density functional theory to investigate the hyperfine and nuclear quadrupole interactions of the basal and axial NV centers. We observed that the four inequivalent NV configurations (hk, kh, hh, and kk) exhibit different electron-nuclear interaction parameters, suggesting that each NV center may act as a separate optically addressable qubit. Finally, we rationalized the observed differences in terms of distinctions in the local atomic structures of the NV configurations. Thus, our results provide the basic knowledge for an extension of quantum protocols involving the 14N nuclear spin.

cond-mat.mtrl-sci↗

arXiv2024

Room Temperature Microsecond Coherence of Silicon Dangling Bonds

Paramagnetic point defects in silicon provide qubits that could open up pathways towards silicon-technology based, low-cost, room-temperature (RT) quantum sensing. The silicon dangling bond (db) is a natural candidate, given its sub-nanometer localization and direct involvement in spin-dependent charge-carrier recombination, allowing for electrical spin readout. In crystalline silicon, however, rapid loss of db spin-coherence at RT due to free-electron trapping, strongly limits quantum applications. In this work, by combining density-functional theory and multifrequency (100 MHz-263 GHz) pulsed electrically detected magnetic resonance spectroscopy, we show that upon electron capture, dbs in a hydrogenated amorphous silicon matrix form metastable spin pairs in a well-defined quasi two-dimensional (2D) configuration. Although highly localized, these entangled spin pairs exhibit nearly vanishing intrinsic dipolar and exchange coupling. The formation of this magic-angle-like configuration involves a >0.3 eV energy relaxation of a trapped electron, stabilizing the pair. This extends RT spin coherence times into the microsecond range in silicon required for a future spin-based quantum sensing technology.

cond-mat.mes-hall↗

arXiv2019

Excited state band mapping and momentum-resolved ultrafast population dynamics in In/Si(111) nanowires investigated with XUV based time- and angle-resolved photoemission spectroscopy

We investigate the excited state electronic structure of the model phase transition system In/Si(111) using femtosecond time- and angle-resolved photoemission spectroscopy (trARPES) with an XUV laser source at 500 kHz . Excited state band mapping is used to characterize the normally unoccupied electronic structure above the Fermi level in both structural phases of indium nanowires on Si(111): the metallic (4x1) and the gapped (8x2) phases. The extracted band positions are compared with the band structure calculated using density functional theory (DFT) within both the LDA and GW approximations. While good overall agreement is found between the GW calculated band structure and experiment, deviations in specific momentum regions may indicate the importance of excitonic effects not accounted for at this level of approximation. To probe the dynamics of these excited states, their momentum-resolved transient population dynamics are extracted. The transient intensities are then simulated by a spectral function determined by a state population employing a transient elevated electronic temperature as determined experimentally. This allows the momentum-resolved population dynamics to be quantitatively reproduced, revealing important insights into the transfer of energy from the electronic system to the lattice. In particular, a comparison between the magnitude and relaxation time of the transient electronic temperature observed by trARPES with those of the lattice as probed in previous ultrafast electron diffraction studies imply a highly non-thermal phonon distribution at the surface following photo-excitation. This suggests the energy from the excited electronic system is initially transferred to high energy optical phonon modes followed by cooling and thermalization of the photo-excited system by much slower phonon-phonon coupling.

cond-mat.str-el↗

arXiv2014

Impurity-mediated early condensation of an atomic layer electronic crystal

While impurity has been known widely to affect phase transitions, the atomistic mechanisms have rarely been disclosed. We directly show in atomic scale how impurity atoms induces the condensation of a representative electronic phase, charge density wave (CDW), with scanning tunneling microscopy. Oxygen impurity atoms on the self-assembled metallic atomic wire array on a silicon crystal condense CDW locally even above the transition temperature, More interestingly, the CDW along the wires is induced not by a single atomic impurity but by the cooperation of multiple impurities. First principles calculations disclose the mechanism of the cooperation as the coherent superposition of the local lattice strain induced by impurities, stressing the coupled electronic and lattice degrees of freedom for CDW. This newly discovered mechanism can widely be applied to various important electronic orders coupled to lattice, opening the possibility of the atomic scale strain engineering.

cond-mat.mes-hall↗