A method for calibrating the relative gamma-ray light yield of plastic scintillators.

Currently we are investigating the inclusion of organotin compounds in new polystyrene scintillator materials to improve full gamma-ray energy sensitivity. Accurate calibration of the relative light yield from the newly developed scintillators is crucial to assess merits of compounds and chemical processes used in the scintillators' development. The full energy gamma-ray peak in a measured gamma-ray spectrum is commonly used in calibrating the relative light yield.

Electronic Properties of Vinylene-Linked Heterocyclic Conducting Polymers: Predictive Design and Rational Guidance from DFT Calculations.

The band structure and electronic properties in a series of vinylene-linked heterocyclic conducting polymers are investigated using density functional theory (DFT). In order to accurately calculate electronic band gaps, we utilize hybrid functionals with fully periodic boundary conditions to understand the effect of chemical functionalization on the electronic structure of these materials. The use of predictive first-principles calculations coupled with simple chemical arguments highlights the critical role that aromaticity plays in obtaining a low band gap polymer.

Improved synthesis of bis(borano)hypophosphite salts.

A synthesis of the bis(borano)hypophosphite anion with various counterions has been developed to make use of more benign and commercially available reagents. This method avoids the use of potentially dangerous reagents used by previous methods and gives the final products in good yield. Details of the crystal structure determination of the sodium salt in space group Ama2 are given using a novel computational technique combined with Rietveld refinement.

Coumarin dyes for dye-sensitized solar cells: A long-range-corrected density functional study.

The excited-state properties in a series of coumarin solar cell dyes are investigated with a long-range-corrected (LC) functional which asymptotically incorporates Hartree-Fock exchange. Using time-dependent density functional theory (TDDFT), we calculate excitation energies, oscillator strengths, and excited-state dipole moments in each of the dyes as a function of the range-separation parameter mu. To investigate the acceptable range of mu and to assess the quality of the LC-TDDFT formalism, an extensive comparison is made between LC-BLYP excitation energies and approximate coupled-cluster singles and doubles calculations.