Article ID Journal Published Year Pages File Type
1228935 Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2016 8 Pages PDF
Abstract

•We obtained symmetrical N-acylsubstituted dihydrazones containing bithiophene core.•We analyze the influence of dihydrazones structure on their physical properties.•They exhibited low electrochemically estimated energy gap (1.72–2.00 eV).•The photovoltaic properties of two bithiophene derivatives as active layer in organic solar cells were studied.•Dihydrazone end-capped with furan rings showed the highest value of PCF (1.68%).

Four symmetrical N-acylsubstituted dihydrazones containing bithiophene core were synthesized from condensation of 2,2′-bithiophene-5,5′-dicarboxyaldehyde with benzoic, isonicotinoyl, 2-thiophenic and 2-furoic hydrazide. The obtained compounds were characterized through the data from 1H nuclear magnetic resonance spectroscopy (NMR), infrared spectroscopy (IR), elemental analysis, UV–vis absorption spectroscopy, photoluminescence (PL), cyclic voltammetry (CV) and differential pulse voltammetry (DPV) measurements. Additionally, the electronic properties including orbital energies and resulting energy gaps were calculated by density functional theory (DFT). Their thermal behavior was investigated by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). They were thermal sable up to 320 °C. The prepared N-acylsubstituted dihydrazones emitted light with λem in the range of 499–530 nm in solution, whereas, in solid state as blend with PMMA blue emission was observed. They undergo quasi-reversible and irreversible electrochemical reduction and oxidation processes, respectively. Additionally, the selected compounds were tested preliminary as component of active layer in organic photovoltaic cells. The highest value of power conversion efficiency, equal to 1.68% under simulated 100 mW/cm2 AM 1.5G irradiation was found for device with the architecture ITO/PEDOT:PSS/P3HT:PCBM:FBTH (1:2:2)/Al.

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Physical Sciences and Engineering Chemistry Analytical Chemistry
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