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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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56 records · Page 4

Properties of the Prompt Optical Counterpart Arising from the Cooling of Electrons in Gamma-Ray Bursts

This work extends a contemporaneous effort to study the properties of the lower-energy counterpart synchrotron emission produced by the cooling of relativistic gamma-ray burst (GRB) electrons through radiation (synchrotron and self-Compton) emission and adiabatic losses. We derive the major characteristics (pulse duration, lag time after burst, and brightness relative to the burst) of the prompt optical counterpart (POC) occurring during or after the GRB. Depending on the magnetic field lifetime, duration of electron injection, and electron transit time Δt o from hard X-ray (GRB) to optical-emitting energies, a POC may appear during the GRB pulse (of duration δt γ ) or after (delayed OC). The signature of counterparts arising from the cooling of GRB electrons is that POC pulses (Δto < δtγ) last as long as the corresponding GRB pulse (δt o ≃ δt γ ), while delayed OC pulses (Δt o > δt γ ) last as long as the transit time (δt o ≃ Δt o ). If OC variability can be measured, then another signature for this OC mechanism is that the GRB variability is passed on to POCs but not to delayed OCs. Within the GRB electron cooling model for counterparts, POCs should be on average dimmer than delayed ones (consistent with the data), and harder GRB low-energy slopes β LE should be associated more often with the dimmer POCs. The latter sets an observational bias against detecting POCs from (the cooling of electrons in) GRBs with a hard slope β LE , making it more likely that the detected POCs of such bursts arise from another mechanism.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗

Nonadiabatic dynamics of photoexcited thiopyridone isomers: An interplay between El-Sayed’s conditions and energy gap law

We investigated the non-adiabatic dynamics of photoexcited thiopyridone systems across their ortho-, meta-, and para-isomeric forms. The relaxation pathways of the three isomers in both gas phase and solvent environments are mapped using surface hopping dynamics based on time-dependent density functional theory. Our analysis highlights the influence of isomeric structures on photophysical behavior, offering insights into design principles to control photochemical phenomena. The simulations suggest a systematic reduction in the rate of intersystem crossing (ISC) from ortho- to meta- to para-isomer. Comparisons with multiconfigurational wave function methods in the gas phase further demonstrate how electronic structure influences the predicted dynamical pathways. The simulated dynamics demonstrates that the spin–orbit coupling strength alone does not determine the rate of ISC, as both state energetics and underlying electronic and structural features play decisive roles. These aspects explain the much slower ISC in the para-isomer, as well as the non-negligible role of the El-Sayed forbidden pathway in the computed ISC dynamics.

Complete-active space self-consistent field↗