Rundel, Kira published the artcileNaphthalene diimide-based small molecule acceptors for organic solar cells, Recommanded Product: 5,5′-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2′-bithiophene, the publication is Journal of Materials Chemistry A: Materials for Energy and Sustainability (2017), 5(24), 12266-12277, database is CAplus.
This work introduces six novel naphthalene diimide (NDI) mol. acceptors for evaluation in organic solar cells based on two different chem. architectures: a star-shaped structure with a triarylamine core flanked by three NDI moieties and a linear mol. composed of a bithiophene bridge between two NDI moieties. For each mol. structure, three different side chains are examined, with alkyl chains linked to the NDI core either through oxygen, sulfur, or nitrogen substituents. Both the chem. structure and the side-chain heteroatom substitution were found to influence the optoelectronic and photovoltaic properties of these mol. acceptors. Organic solar cells were fabricated with each acceptor, utilizing PBDTTT-EFT (also known as PTB7-Th) as the donor material in inverted bulk-heterojunction devices. Nitrogen was observed to lower the solar cell performance for these acceptors by significantly decreasing the short circuit c.d. (JSC), while sulfur increased the JSC and, in the star configuration, led to the highest power conversion efficiency (PCE) of 2.8% – which is amongst the highest for any mol. NDI-based acceptor to date. Grazing incidence wide-angle x-ray scattering (GIWAXS) measurements of the star-shaped materials showed the side-chain substitutional atom significantly alters the material’s packing configuration in neat films, with films blended with PBDTTT-EFT showing features characteristic of the neat donor and acceptor materials, indicating that the small mols. do not disrupt the packing of PBDTTT-EFT (and vice versa). Resonant soft x-ray scattering (R-SoXS) measurements indicate the PBDTTT-EFT:star-shaped acceptor blends are not subject to coarse phase-separation, with the average domain size for all three star-shaped acceptor blends typically being <100 nm. This is confirmed by similar topog. for blended films in AFM images amongst the three acceptors. Photoluminescence (PL) quenching measurements, however, found large differences in PL quenching efficiency which were attributed to differences in the driving force for charge transfer, with the nitrogen substituted compound showing the lowest PL quenching and the sulfur replacement showing the highest.
Journal of Materials Chemistry A: Materials for Energy and Sustainability published new progress about 239075-02-6. 239075-02-6 belongs to alcohols-buliding-blocks, auxiliary class Thiophene,Boronic acid and ester,Boronate Esters, name is 5,5′-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2′-bithiophene, and the molecular formula is C20H28B2O4S2, Recommanded Product: 5,5′-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2′-bithiophene.
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