Título: ORGANIC ELECTRONICS Pesquisar Publicações da Revista

Vol. 49

Páginas: 194-205

ISSN: 1566-1199

Editora: Elsevier

ISI Web of Knowledge - 8 Citações

ISI Web of Science

Scopus - 13 Citações

INSPEC

CORDIS: Ciências Físicas > Química > Química orgânica

ID Authenticus: P-00M-ZG6

DOI: 10.1016/j.orgel.2017.06.048

Resumo (PT):

Abstract (EN): Five push-pull heterocyclic dyes 4-7, and 9 were synthesized and characterized in order to study the variations in the optical, electronic and photovoltaic properties induced by structural modifications, i.e. different spacer units and anchoring groups. The final push-pull conjugated dyes 6-7 and 9 are formed by a N,N-dimethylaniline donor moiety conjugated with bithiophene, ethynyl-bithiophene or ethynylthieno[3,2-b] thiophene spacers and cyanoacetic acid or rhodanine-3-acetic acid as anchoring group. The synthesis of the precursor aldehydes 4-5 was accomplished through a Sonogashira coupling, on the other hand, compound 8 was prepared by Suzuki coupling. Knoevenagel condensation of aldehydes 4, 5 and 8 with cyanoacetic acid or rhodamine-3-acetic acid afforded the final push-pull dyes 6, 7 and 9. Information on conformation, electronic structure and electron distribution was obtained by DFT and TDDFT calculations. This multidisciplinary study regarding the evaluation of the optical, redox and photovoltaic properties of the dyes reveals that compound 7, bearing an ethynyl-bithiophene spacer conjugated with a cyanoacetic acid anchoring group, has the highest conversion efficiency (3.51%) as dye sensitizer in nanocrystalline TiO2 solar cells. Co-adsorption studies were also performed for dyes 6-7 with N719 as co-adsorbent, and this enhanced dye efficiencies by 33e45%. The best cell performance was obtained by co-adsorbing N719 and dye 7 (75/25 vol%) with 4.66% efficiency.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 12