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Shridhar Sanjay Shanbhag

Publications and source records attributed to Shridhar Sanjay Shanbhag.

2 recordsLinked to original sources

CP2K: An electronic structure and molecular dynamics software package - Dynamics, Transport, and Spectroscopic Response

One of the distinguishing aspects of CP2K is its seamless integration of diverse structural and transition-state optimization techniques with advanced sampling approaches including Monte Carlo, molecular dynamics, and metadynamics, enabling the efficient exploration of complex potential- and free-energy landscapes, including rare events. These capabilities are combined with a broad hierarchy of energy and force evaluation methods, ranging from classical and machine-learned interaction potentials and mixed quantum-classical multiscale and semiempirical schemes, to highly accurate quantum-mechanical electronic-structure approaches. At the heart of the latter lies the Gaussian and plane-wave framework, along with its augmented all-electron generalization, which have been described in detail in our previous code review [T. D. Kühne et al., J. Chem. Phys. 152, 194103 (2020)]. Building on this foundation, the present work revisits the methods within CP2K that turn electronic structure into dynamics, transport, and spectroscopic response. Particular emphasis is placed on the coupling between static response calculations and nuclear motion: spectra may be evaluated at optimized structures, averaged over thermally sampled configurations, obtained from time-correlation functions along ab-initio or path integral molecular trajectories, or followed in real time together with electronic and nuclear dynamics. The same modular structure also enables equilibrium and biased transport simulations, from Kubo-type linear response to open-boundary approaches under external potentials, highlighting CP2K's unique capability to unify quantum chemistry with quantum and statistical mechanics within a versatile, holistic simulation environment.

physics.chem-ph↗

Direct measurement of broken time-reversal symmetry in centrosymmetric and non-centrosymmetric atomically thin crystals with nonlinear Kerr rotation

Time-reversal symmetry, together with space-inversion symmetry, is one of the defining properties of crystals, underlying phenomena such as magnetism, topology and non-trivial spin textures. Transition metal dichalcogenides (TMDs) provide an excellent tunable model system to study the interplay between time-reversal and space-inversion symmetry, since both can be engineered on demand by tuning the number of layers and via all-optical bandgap modulation. In this work, we modulate and study time-reversal symmetry using third harmonic Kerr rotation in mono- and bilayer TMDs. By illuminating the samples with elliptically polarized light, we achieve spin-selective bandgap modulation and consequent breaking of time-reversal symmetry. The reduced symmetry modifies the nonlinear susceptibility tensor, causing a rotation of the emitted third harmonic polarization. With this method, we are able to probe broken time-reversal symmetry in both non-centrosymmetric (monolayer) and centrosymmetric (bilayer) crystals. Furthermore, we discuss how the detected third harmonic rotation angle directly links to the spin-valley locking in monolayer TMDs and to the spin-valley-layer locking in bilayer TMDs. Thus, our results define a powerful approach to study broken time-reversal symmetry in crystals regardless of space-inversion symmetry, and shed light on the spin, valley and layer coupling of atomically thin semiconductors.

physics.optics↗