Langmuir–Blodgett Films of Self-Assembled (Alkylether-Derivatized Zn Phthalocyanine)–(C60 Imidazole Adduct) Dyad with Controlled Intermolecular Distance for Photoelectrochemical Studies

• Published in: ACS applied materials & interfaces Vol. 6; no. 11; pp. 8688 - 8701
• Main Authors: Obraztsov, Ievgen, Noworyta, Krzysztof, Hart, Aaron, Gobeze, Habtom B, KC, Chandra B, Kutner, Wlodzimierz, D’Souza, Francis
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 11.06.2014
• Subjects: photoelectrochemistry; imidazole adduct of C60; Langmuir−Blodgett film; zinc phthalocyanine; supramolecular assembling; donor−acceptor dyad; C60 fullerene
• ISSN: 1944-8244; 1944-8252
• DOI: 10.1021/am501446g

A multilayer Langmuir–Blodgett (LB) film of the self-assembled electron donor–acceptor dyad of Zn phthalocyanine, appended with four long-chain aliphatic ether peripheral substituents, and an imidazole adduct of C60 was prepared and applied as a photoactive material in a photoelectrochemical cell. Changes in the simultaneously recorded surface pressure and surface potential vs area per molecule compression isotherms for Langmuir films of the dyad and, separately, of its components helped to identify phase transitions and mutual interactions of molecules in films. The Brewster angle microscopy (BAM) imaging of the Langmuir films showed circular condensed phase domains of the dyad molecules. The determined area per molecule was lower than that estimated for the dyad and its components, separately. The multilayer LB films of the dyad were transferred onto hydrophobized fluorine-doped tin oxide-coated (FTO) glass slides under different conditions. The presence of both components in the dyad LB films was confirmed with the UV–vis spectroscopy measurements. For the LB films transferred at different surface pressures, the PM-IRRAS measurements revealed that the phthalocyanine macrocycle planes and ether moieties in films were tilted with respect to the FTO surface. The AFM imaging of the LB films indicated formation of relatively uniform dyad LB films. Then, the femtosecond transient absorption spectral studies evidenced photoinduced electron transfer in the LB film. The obtained transient signals corresponding to both Zn­(TPPE) •+ and C60im •– confirmed the occurrence of intramolecular electron transfer. The determined rate constants of charge separation, k cs = 2.6 × 1011 s–1, and charge recombination, k cr = 9.7 × 109 s–1, indicated quite efficient electron transfer within the film. In the photoelectrochemical studies, either photoanodic or photocathodic current was generated depending on the applied bias potential when the dyad LB film-coated FTO was used as the working electrode and ascorbic acid or methylviologen, respectively, as the charge mediator in an aqueous solution.