1293967-24-4

Upstream product

• 1293967-22-2 (4-p-tolyl-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indol-7-yl)boronic acid 
• 86232-66-8 4-bromo-1,8-naphthaloyl-glycine methyl ester 

Downstream Products

• 1293967-26-6 C₃₂H₂₆N₂O₄ 

Relevant academic research and scientific papers

Novel dyes based on naphthalimide moiety as electron acceptor for efficient dye-sensitized solar cells

Four novel naphthalimide-based dyes (D-1, D-2, D-3 and D-4) were synthesized and utilized as sensitizers in dye-sensitized solar cells (DSCs), in which the triphenylamine (TPA) or indoline groups, naphthalimide unit and carboxylic group were functionalized as electron donor, acceptor and anchoring group, respectively. The naphthalimide unit was employed as the π-conjugation ring and electron acceptor for effectively realizing intramolecular charge separation in the oxidized states. In the series of dyes, the LUMO orbital is delocalized mainly on naphthalimide moieties, especially on the carbonyl group. Consequently, the LUMO electrons are isolated from the carboxyl anchoring group (-CH2CO2H) due to the presence of the methylene group, which could suppress the electron injection efficiency from the excited dyes to the TiO2 conduction band, thus leading to the inferior efficiencies of 1.10, 1.18, 2.27 and 2.70%, respectively, even though they exhibit broad spectral response and high extinction coefficients.