Synthesis of Silatrane-Containing Organic Sensitizers as Precursors for the Silyloxyl Anchoring Group in Dye-Sensitized Solar Cells
Anno: 2017
Autori: Bessi M., Monini M., Calamante M., Mordini A., Sinicropi A., Basosi R., Di Donato M., Foggi P., Iagatti A., Zani L., Reginato G.
Affiliazione autori: CNR, Ist Chim Composti Organometall, ICCOM, Via Madonna del Piano 10, I-50019 Sesto Fiorentino, Italy; Univ Siena, Dipartimento Biotecnol Chim & Farm, Via A Moro 2, I-53100 Siena, Italy; Univ Firenze, Dipartimento Chim U Schiff, Via Lastruccia 13, I-50019 Sesto Fiorentino, Italy; INO, Enrico Fermi 6, Florence, Italy; Univ Perugia, Dipartmento Chim, Via Elce di Sotto 8, I-06123 Perugia, Italy; LENS European Lab Nonlinear Spectroscopy, Via N Carrara 1, I-50019 Sesto Fiorentino, Italy.
Abstract: A series of organic D-?-A dyes, endowed with different silicon-based anchoring groups, has been prepared to assess the stability of such anchoring moieties on nanocrystalline TiO2 in dye-sensitized solar cells. Due to the difficulties encountered in finding a reliable and robust preparation protocol to obtain pure trialkoxysilanes, replacement with a silatrane moiety was evaluated. It was found that the silatrane group could be easily introduced on three different molecular scaffolds by using a simple amide coupling reaction mediated by EDC-Cl. Furthermore, the spectroscopic properties and anchoring mode on nanocrystalline TiO2 of the silatrane dyes were found to be nearly identical to those of the trialkoxysilane compounds, and both gave a much more stable attachment to the semiconductor compared with their cyanoacrylic acid counterpart, as shown by desorption experiments.
Giornale/Rivista: SYNTHESIS-STUTTGART
Volume: 49 (17) Da Pagina: 3975 A: 3984
Parole chiavi: organic dyes, trialkoxysilane, silatrane, UV/Vis spectroscopy, ATR-IR, dye-sensitized solar cellsDOI: 10.1055/s-0036-1588836Citazioni: 2dati da “WEB OF SCIENCE” (of Thomson Reuters) aggiornati al: 2024-10-06Riferimenti tratti da Isi Web of Knowledge: (solo abbonati) Link per visualizzare la scheda su IsiWeb: Clicca quiLink per visualizzare la citazioni su IsiWeb: Clicca qui