arXiv subjects

Jaladhar Mahato

Publications and source records attributed to Jaladhar Mahato.

3 recordsLinked to original sources

arXiv2026

From microscopic fluctuations to susceptibility spectra: single-molecule relaxation in glassy media

Single-molecule (SM) rotational dynamics of fluorescent probes in polystyrene near the glass transition temperature ($T_g$) are investigated over long times to reconstruct susceptibility spectra. The loss spectrum, commonly recorded using external field-driven (frequency-domain) spectroscopy, such as dielectric spectroscopy, is reconstructed from purely thermal SM rotational fluctuations. The results reproduce time-temperature superposition typically seen in dielectric spectroscopy for materials near $T_g$ and show that the ensemble spectrum is comprised of individual molecular responses to distinct environments.

cond-mat.soft↗

arXiv2025

Anomalous Translational Dynamics of Molecular Probes Near the Polymer Glass Transition

The origin of the dramatic slowdown of dynamics near the glass transition temperature (Tg) remains a long-standing fundamental and unresolved issue in soft condensed matter. While single-molecule (SM) experiments using fluorescent probes have provided critical insight for molecular and polymeric glass formers through rotational measurements, translational dynamics remain largely unexplored in such systems at the molecular length scale. Here, we report SM translational dynamics of molecular probes in high molecular weight polystyrene at three temperatures near Tg. The probes exhibit quasi-stationary position fluctuations, non-Gaussian displacement distributions, sub-diffusive transport with anti-correlated displacements, and a characteristic translational relaxation time. The observations are quantitatively described using a microscopic framework based on the generalized Langevin equation and supported by numerical modeling for heterogeneous transport. The translational dynamics of the probes provides direct microscopic evidence of dynamic heterogeneity and suggests a pathway to more fully understand glassy dynamics in glass formers near Tg.

cond-mat.soft↗

arXiv2018

Photoluminescence Blinking beyond Quantum-Confinement: Spatiotemporally Correlated Intermittency over Entire Micron Sized Perovskite Polycrystalline Disks

Abrupt fluorescence intermittency or blinking is long recognized to be characteristic of single nano-emitters. Extended quantum-confined nanostructures also undergo spatially heterogeneous blinking, however, there is no such precedence in dimensionally unconfined (bulk) materials. Here, we report multi-level blinking of entire individual organo-lead bromide perovskite micro-crystals (volume 0.1-3 micron-cuble) under ambient conditions. Extremely high spatiotemporal correlation (>0.9) in intra-crystal emission intensity fluctuations signifies effective communication amongst photogenerated carriers at distal locations (up to ~4 microns) within each crystal. Fused polycrystalline grains also exhibit this intriguing phenomenon, which is rationalized by correlated and efficient migration of carriers to a few transient non-radiative traps, the nature and population of which determine blinking propensity. Observation of spatiotemporally correlated emission intermittency in bulk semiconductor crystals opens up the possibility to design novel devices involving long range (mesoscopic) electronic communication.

cond-mat.mes-hall↗