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Ramachandra Bangari

Publications and source records attributed to Ramachandra Bangari.

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Geometric Control of Visible Emitter Creation in Hexagonal Boron Nitride by Oblique Ion Irradiation

Ion irradiation creates optically active defects in wide-bandgap van der Waals materials, yet most approaches tune defect formation by varying the ion species, energy, or fluence while leaving the incidence geometry fixed. The ion-incidence angle is established here as a geometric control parameter for engineering visible emitters in hexagonal boron nitride (hBN). The angle and ion fluence of a plasma-focused heavy-ion (Xe+) beam are varied across hBN flakes of different thickness, and the resulting photoluminescence is quantified. In thick flakes, oblique irradiation shifts the fluence for maximum emission by nearly two orders of magnitude relative to normal incidence, whereas thin flakes exhibit an angle-independent optimum. Ion-trajectory simulations attribute this thickness dependence to lateral redistribution of the collision cascade and enhanced oblique sputtering. Atomic force microscopy identifies distinct processing regimes that delineate the useful defect-creation window. Post-irradiation annealing quenches the emission and shifts the spectral weight toward the green-yellow band while preserving the angle-dependent activation trends. Spectrally resolved lifetime measurements show comparable biexponential dynamics for normal and oblique incidence, consistent with emission from related defect families rather than a geometry-specific emitter species. These results establish ion-incidence geometry as a materials-level knob for programming optical defect activation and spatial defect distributions in van der Waals photonic materials.

physics.optics

Tailoring phonon-driven responses in α-MoO3 through isotopic enrichment

The implementation of polaritonic materials into nanoscale devices requires selective tuning of parameters to realize desired spectral or thermal responses. One robust material is α-MoO3, which as an orthorhombic crystal boasts three distinct phonon dispersions, providing three polaritonic dispersions of hyperbolic phonon polaritons (HPhPs) across the mid-infrared (MIR). Here, the tunability of both optical and thermal responses in isotopically enriched α-MoO3 (98MoO3, Mo18O3 and 98Mo18O3) are explored. A uniform ~5 % spectral redshift from 18O enrichment is observed in both Raman- and IR-active TO phonons. Both the in- and out-of-plane thermal conductivities for the isotopic variations are reported. Ab initio calculations both replicate experimental findings and analyze the select-mode three-phonon scattering contributions. The HPhPs from each isotopic variation are probed with s-SNOM and their Q- factors are reported. A Q-factor maxima increase of ~50 % along the [100] in the RB2 and ~100 % along the [001] in the RB3 are reported for HPhPs supported in 98Mo18O3. Observations in both real and Fourier space of higher-order HPhP modes propagating in single slabs of isotopically enriched α-MoO3 without the use of a subdiffractional surface scatterer are presented here. This work illustrates the tunability of α-MoO3 for thermal and nanophotonic applications.

cond-mat.mtrl-sci