SearcharxivSearch

arXiv subjects

Eric L. Chronister

Publications and source records attributed to Eric L. Chronister.

2 recordsLinked to original sources

Spectroscopic Evidence of Low Energy Gaps Persisting Towards 120 Kelvin in Surface-Doped p-Terphenyl Crystals

The possibility of high temperature superconductivity in organic compounds has been discussed since the pioneering work of Little in 1964, with unsatisfactory progress until the recent report of a weak Meissner shielding effect at 120 Kelvin in potassium-doped para-terphenyl samples. To date however, no other signals of the superconductivity have been shown, including the zero-resistance state or evidence for the formation of the Cooper pairs that are inherent to the superconducting state. Here, using high-resolution photoemission spectroscopy on potassium surface-doped para-terphenyl crystals, we uncover low energy gaps that persist to approximately 120 K. Among a few potential origins for these gaps, we argue that the onset of electron pairing within molecules is most likely. And while pairing gaps are a prerequisite for high temperature superconductivity they do not guarantee it. Rather, the development of long-range phase coherence between the paired states on the molecules is necessary, requiring good wavefunction overlap between molecular states--something that is in general difficult for such weakly overlapping molecules.

cond-mat.supr-con

Ultrafast studies on the photophysics of matrix-isolated radical cations of polycyclic aromatic hydrocarbons: implications for the Diffuse Interstellar Bands (DIB) problem

Rapid, efficient deactivation of the photoexcited PAH cations accounts for their remarkable photostability and have important implications for astrochemistry, as these cations are the leading candidates for the species responsible for the diffuse interstellar bands (DIB) observed throughout the Galaxy.Ultrafast relaxation dynamics for photoexcited PAH cations isolated in boric acid glass have been studied using femtosecond and picosecond transient grating spectroscopy. With the exception of perylene+, the recovery kinetics for the ground doublet (D0) states of these radical cations are biexponential, containing a fast (< 200 fs) and a slow (3-20 ps) components. No temperature dependence or isotope effect was observed for the fast component, whereas the slow component exhibits both the H/D isotope effect (1.1-1.3) and strong temperature dependence (15 to 300 K). We suggest that the fast component is due to internal Dn to D0 conversion and the slow component is due to vibrational energy transfer (VET) from a hot D0 state to the glass matrix.

astro-ph