arXiv subjects

Sarang Yeola

Publications and source records attributed to Sarang Yeola.

4 recordsLinked to original sources

arXiv2026

Photonic-Crystal Microresonator Frequency Combs in the O-band

Photonic-crystal microresonators (PhCRs) are a powerful platform for generating Kerr frequency combs. Because Kerr-soliton dynamics in PhCRs are largely decoupled from the operating wavelength, the comb output can be engineered through customization of the device layer. Here, we demonstrate a tantalum pentoxide (tantala) PhCR platform that supports 1310 nm and 1550 nm band operation, and we explore high-efficiency O-band soliton microcombs with all-semiconductor laser pumps. We engineer the PhCRs with silicon dioxide cladding and normal dispersion with intrinsic quality factors exceeding $7\times10^{6}$. By pumping bandgap modes, we obtain robust and efficient soliton comb formation at a 200 GHz mode spacing. Our PhCRs enable systematic tuning from narrowband to broadband comb states within a single device geometry. The combs exhibit low relative intensity noise approaching the shot-noise limit, indicating stable phase-matching in the PhCR. Using a second resonator coupler, we amplify the comb output off-chip, demonstrating a pathway to high-power O-band sources. These results establish PhCR engineering in the tantala platform as a scalable approach to wavelength-agile, low-noise microcombs for applications in communications, sensing, and signaling.

physics.optics↗

arXiv2026

Nanophotonic control of collective many-body states in Kerr solitons

Spatially periodic systems of coupled bosons are governed by on-site interactions and tunneling between sites, opening a rich phase space of many-body behavior. Here, we explore nanophotonic control of collective many-body light states in a driven-dissipative Kerr microresonator. We demonstrate a non-equilibrium Mott insulator to superfluid transition that arises from the interplay of spatially local Kerr interactions that generate and mediate interference among discrete frequency modes. A photonic-crystal (PhC) lattice bandgap inscribed on the resonator controls linear mode coupling while preserving self-mode Kerr interactions. By increasing the PhC bandgap, we suppress nonlinear cross-mode coupling to access the Mott-insulator phase, wherein the soliton spectrum forms a flattop frequency comb with large and uniform power per mode. In contrast, reducing the PhC bandgap restores cross-mode coupling and drives a delocalized superfluid regime characterized by long-range phase coherence and a spectrum with non-uniform power distribution. Our work shows that many-body physics creates collective states in driven-dissipative systems, enabling advances in programmable photonics and quantum-optical computing.

physics.optics↗

arXiv2024

Generalized Einstein Relations between Absorption and Emission Spectra at Thermodynamic Equilibrium

We present Einstein coefficient spectra and a detailed-balance derivation of generalized Einstein relations between them that is based on the connection between spontaneous and stimulated emission. If two broadened levels or bands overlap in energy, transitions between them need not be purely absorptive or emissive. Consequently, spontaneous emission can occur in both transition directions, and four Einstein coefficient spectra replace the three Einstein coefficients for a line. At equilibrium, the four different spectra obey five pairwise relationships and one lineshape generates all four. These relationships are independent of molecular quantum statistics and predict the Stokes' shift between forward and reverse transitions required by equilibrium with blackbody radiation. For Boltzmann statistics, the relative strengths of forward and reverse transitions depend on the formal chemical potential difference between the initial and final bands, which becomes the standard chemical potential difference for ideal solutes. The formal chemical potential of a band replaces both the energy and degeneracy of a quantum level. Like the energies of quantum levels, the formal chemical potentials of bands obey the Rydberg-Ritz combination principle. Each stimulated Einstein coefficient spectrum gives a frequency-dependent transition cross section. Transition cross sections obey causality and a detailed-balance condition with spontaneous emission, but do not directly obey generalized Einstein relations. Even with an energetic width much less than the photon energy, an absorptive forward transition with an energetic width much greater than the thermal energy can have such an extreme Stokes' shift that its reverse transition cross section becomes predominantly absorptive rather than emissive.

physics.chem-ph↗

arXiv2018

Single-shot Ultrafast Imaging via Spatiotemporal Division of Femtosecond Laser Pulses

We have developed a single-shot imaging technique that can capture ultrafast events occurring on femtosecond to picosecond time scales. The technique is based on an optical pump-probe method, in which multiple time-delayed femtosecond pulses simultaneously probe a pump-excited sample. Here we use two sets of 2-by-2 mirror arrays for spatial/temporal division and routing of multiple probe pulses. This single-shot scheme is successfully applied to capture femtosecond ionization fronts propagating at the speed of light in air, as well as laser-induced ablation of solid targets.

physics.ins-det↗