Electrochemical and photoelectronic studies on C60-pyrrolidine- functionalised poly(terthiophene)
RIS ID
92676
Abstract
A novel donor-acceptor poly(terthiophene) derivative bearing a C60 pendant was electropolymerizated from N-methyl-2-(2-[4,4′'-didecyloxy-2,2′;5′,2′']terthiophen-3′-yl-ethenyl)fullero[3,4]pyrrolidine (TTh-C60) solution. The electroreduction of TTh-C60 and poly(TTh-C60) showed the presence of complex peaks related to fulleropyrrolidine reduction. The dual nature of these redox couples may be related to increasing Coulombic repulsion or coupling between C60 substituents. Electrochemical, X-Ray photoelectron spectroscopy (XPS), Ultra-Violet photoelectron (UPS) and UV-Vis spectroscopy also confirm the nature of poly(TTh-C60). Electrochemical band gap of poly(TTh-C60) is 0.63 ± 0.20 eV in TBAP electrolyte and propylene carbonate (PC) solution. Furthermore, we obtained the value of optical energy band gap (Eopt = 0.59 ± 0.03 eV), the transport energy band gap (Egtrans = 1.17 ± 0.20 eV) and the exciton binding energy (Eb = 0.58 ± 0.20 eV) for poly(TTh-C60). The ionization energy values (IE) were determined using UPS spectroscopy (IE = 4.92 ± 0.10 eV) and electrochemical investigations of the poly(TTh-C60) polarized in TBAP/DCM (IE = 5.01 ± 0.10 eV) and TBAP/PC solution (IE = 4.95 ± 0.10 eV) demonstrating good coincidence of the value. The electrochemical method revealed, that the location of the Fermi level relative to the valence and conduction bands indicates p-type character of semiconducting poly(TTh-C60). On the other hand photoemission spectroscopy manifests n-type behavior of examined sample. In turn, the UV-Vis result showed that the charge transfer (CT) between poly(TTh) and C60 unit can suggest, that these chromophores are not entirely independent.
Publication Details
Czichy, M., Wagner, P., Grzadziel, L., Krzywiecki, M., Szwajca, A., Lapkowski, M., Zak, J. & officer, D. L. (2014). Electrochemical and photoelectronic studies on C60-pyrrolidine- functionalised poly(terthiophene). Electrochimica Acta, 141 51-60.