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M. Upadhyay Kahaly

Publications and source records attributed to M. Upadhyay Kahaly.

4 recordsLinked to original sources

Energetic, tunable, highly-elliptically polarized higher harmonics generated by intense two-color counter rotating laser fields

In this work, we demonstrate experimentally the efficient generation and tunability of energetic highly-elliptical high-harmonics in Ar gas, driven by intense two-color counter rotating laser electric fields. A bi-chromatic beam tailored by a MAZEL-TOV apparatus generates HHG, where the output spectrum of the highly elliptical HHG radiation can be tuned for a energy range of \DeltaE\HF150meV in the spectral range of ~20 eV with energy per pulse EXUV~400 nJ at the source. Furthermore we employ time-dependent density functional simulations to probe in-depth the dependence of the harmonic ellipticity and the strength of the isolated atto pulses on the driving field parameters and demonstrate the robustness of the HHG with the bichromatic field. We show how by properly tuning the central frequency of the second harmonic, the central frequency of the extreme ultraviolet (XUV) high harmonic radiation is continuously tuned. The demonstrated energy values largely exceed the output energy from many other laser driven attosecond sources reported so far and prove to be sufficient for inducing (along with tight XUV focusing geometries) the nonlinear processes in the atomic system. We envisage that such tunable energetic highly-elliptical HHG spectra can remove the facility restrictions from requirements of few-cycle driving pulses for isolated circular attosecond pulse generation.

physics.optics↗

Quantum path interferences in high-order harmonic generation from aligned diatomic molecules

Electron quantum path interferences in strongly laser-driven aligned molecules and their dependence on the molecular alignment is an essential open problem in strong-field molecular physics. Here, we demonstrate an approach which provides direct access to the observation of these interference processes. The approach is based on the combination of the time-gated-ion-microscopy technique with a pump-probe arrangement used to align the molecules and generate high-order harmonics. By spatially resolving the interference pattern produced by the spatiotemporal overlap of the harmonics emitted by the short and long electron quantum paths, we have succeeded in measuring in situ their phase difference and disclose their dependence on molecular alignment. The findings constitute a vital step towards an understanding of strong-field molecular physics and the development of attosecond spectroscopy approaches without the use of auxiliary atomic references.

physics.atom-ph↗

Modelling magnetism of C at O and B monovacancies in graphene

The presence of defects can introduce important changes in the electronic structure of graphene, leading to phenomena such as C magnetism. In addition, vacancies are reactive and permit the incorporation of dopants. This paper discusses the electronic properties of defective graphene for O and B decoration. Phonon calculations allow us to address directly the stability of the systems under study. We show that it is possible to obtain magnetic solutions with and without dangling bonds, demonstrating that C magnetism can be achieved in the presence of B and O.

cond-mat.mes-hall↗

Induced magnetism in transition metal intercalated graphitic systems

We investigate the structure, chemical bonding, electronic properties, and magnetic behavior of a three-dimensional graphitic network in aba and aaa stacking with intercalated transition metal atoms (Mn, Fe, Co, Ni, and Cu). Using density functional theory, we find induced spin-polarization of the C atoms both when the graphene sheets are aba stacked (forming graphite) and aaa stacked (resembling bi-layer graphene). The magnetic moment induced by Mn, Fe, and Co turns out to vary from 1.38 μB to 4.10 μB, whereas intercalation of Ni and Cu does not lead to a magnetic state. The selective induction of spin-polarization can be utilized in spintronic and nanoelectronic applications.

cond-mat.mes-hall↗