Polaritonic Enhancement of Near-field Scattering of Small Molecules Encapsulated in Boron Nitride Nanotubes

Near-field spectroscopy has been extensively applied recently to analyze collective optical properties of materials at the nanoscale. However, vibrations of small molecules were only recognizable in close proximity to a metallic resonator. We show that encapsulation in boron nitride nanotubes (BNNT) enhances the near-field vibrational spectra of C$_{60}$ fullerene, reaching a sensitivity limit of a few hundred molecules. Furthermore, products of chemical reactions inside the tubes can be identified, so long as their vibrational signatures lie in the polariton gap of the BNNT.Comment: 7 pages, 4 figure

Mott localization in the correlated superconductor Cs3C60 resulting from the molecular Jahn-Teller effect

Cs3C60 is a correlated superconductor under pressure, but an insulator under ambient conditions. The mechanism causing this insulating behavior is the combination of Mott localization and the dynamic Jahn-Teller effect. We show evidence from infrared spectroscopy for the dynamic Jahn-Teller distortion. The continuous change with temperature of the splitting of infrared lines is typical Jahn-Teller behavior, reflecting the change in population of solid-state conformers. We conclude that the electronic and magnetic solid-state properties of the insulating state are controlled by molecular phenomena. We estimate the time scale of the dynamic Jahn-Teller effect to be above 10^(-11) s and the energy difference between the conformers less than 20 cm-1

Optimized unconventional superconductivity in a molecular Jahn-Teller metal

Understanding the relationship between the superconducting, the neighboring insulating, and the normal metallic state above Tc is a major challenge for all unconventional superconductors. The molecular A3C60 fulleride superconductors have a parent antiferromagnetic insulator in common with the atom-based cuprates, but here, the C603– electronic structure controls the geometry and spin state of the structural building unit via the on-molecule Jahn-Teller effect. We identify the Jahn-Teller metal as a fluctuating microscopically heterogeneous coexistence of both localized Jahn-Teller–active and itinerant electrons that connects the insulating and superconducting states of fullerides. The balance between these molecular and extended lattice features of the electrons at the Fermi level gives a dome-shaped variation of Tc with interfulleride separation, demonstrating molecular electronic structure control of superconductivity

The Impact of International Remittances on Income, Work Efforts, Poverty and Inequality: Evidence from Vietnam

This study provides new empirical evidence on the impact of international remittances. Using data from the two most recent Vietnam Household and Living Standard Surveys, the paper estimates the effect of remittances on per capita income, per capita expenditure, work efforts, poverty and inequality. The estimates suggest that a rise in international remittances in Vietnam increases household income and expenditure. Yet, the study also finds evidence that international remittances may create a moral hazard problem by inducing disincentives to work. Moreover, the study suggests that international remittances, at the least in the short run, do not reduce poverty. They may even lead to an increase in inequality. Overall, the study casts doubts on the view that international remittances may play a crucial role in reducing poverty in developing countries

Low band gap and ionic bonding with charge transfer, threshold in the polymeric lithium fulleride Li(4)C(60)

We demonstrate the growth of crystalline Li(4)C(60) films. The low-energy electron diffraction pattern of the films indicates the formation of polymer chains in the plane of the surface, consistent with the reported crystal structure. Electron energy loss and photoemission spectra identify the Li(4)C(60) polymer as a low band gap semiconductor, with a relatively strong coupling of electrons to low-frequency stretching modes of the polymer bonds and alkali phonons. No evidence is found for hybridization between the Li- and fullerene-derived electronic states. Instead, a partial charge transfer takes place, which is the same for different Li concentrations. This result rationalizes the stability of the polymer phase over a wide range of stoichiometries