Acceptor–donor–acceptor small molecules based on derivatives of 3,4-ethylenedioxythiophene for solution processed organic solar cells

Three simple semiconducting acceptor–donor–acceptor (A–D–A) small molecules based on an electron-rich (3,4-ethylenedioxythiophene) EDOT central core have been synthesised (DIN-2TE, DRH-2TE, DECA-2TE) and characterised. Organic photovoltaic (OPV) devices incorporating these materials have been prepared and evaluated. The physical properties of the molecules were characterised by TGA, DSC, UV/vis spectroscopy and cyclic voltammetry. The optical HOMO–LUMO energy gaps of the molecules in the solid state were in the range 1.57–1.82 eV, and in solution 1.88–2.04 eV. Electrochemical HOMO–LUMO energy gaps determined by cyclic voltammetry were found to be in the range 1.97–2.31 eV. The addition of 1% 1,8-diiodooctane (DIO) to photoactive blends of the A–D–A molecules and PC71BM more than doubled the power conversion efficiency (PCE) in the case of DRH-2TE:PC71BM devices to 1.36%

Acceptor-donor-acceptor small molecules based on derivatives of 3,4-ethylenedioxythiophene for solution processed organic solar cells

Three simple semiconducting acceptor-donor-acceptor (A-D-A) small molecules based on an electron-rich (3,4-ethylenedioxythiophene) EDOT central core have been synthesised (DIN-2TE, DRH-2TE, DECA-2TE) and characterised. Organic photovoltaic (OPV) devices incorporating these materials have been prepared and evaluated. The physical properties of the molecules were characterised by TGA, DSC, UV/vis spectroscopy and cyclic voltammetry. The optical HOMO-LUMO energy gaps of the molecules in the solid state were in the range 1.57-1.82 eV, and in solution 1.88-2.04 eV. Electrochemical HOMO-LUMO energy gaps determined by cyclic voltammetry were found to be in the range 1.97-2.31 eV. The addition of 1% 1,8-diiodooctane (DIO) to photoactive blends of the A-D-A molecules and PC71BM more than doubled the power conversion efficiency (PCE) in the case of DRH-2TE:PC71BM devices to 1.36%

Expanding the Solid-State Landscape of l

To date, only one crystal structure of l-phenylalanine has been reported, with no confirmed report of polymorphism of this material. In the present work, we report the discovery of a new polymorph of l-phenylalanine, with the structural properties determined directly from powder X-ray diffraction data. The new polymorph of l-phenylalanine is stable only under rigorously dry conditions. In addition, two new solid hydrate phases of l-phenylalanine have been discovered: a monohydrate and a hemihydrate. The hemihydrate is susceptible to partial water deficiency. The crystal structures of the monohydrate and hemihydrate phases have also been determined directly from powder X-ray diffraction data. On the basis of results from dynamic vapor sorption and other experiments, we demonstrate that the three new solid forms are readily interconvertible as a function of relative humidity