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Structure-dependent optical anisotropy of porphyrin Langmuir-Schaefer films

Year: 2002

Journal: Surface Science 521 (2002) L645-L649, 20111221

Authors: C. Goletti , G. Bussetti , P. Chiaradia , R. Paolesse , A. Froiio , E. Dalcanale , T. Berzina , C. Di Natale , A. D_Amico

Organizations: a Dipartimento di Fisica and Uniti INFM, Universita di Roma "Tor Vergata", Via della Ricerca Scienti.ca 1, 00133 Roma, Italy b Dipartimento di Scienze e Tecnologie Chimiche, Universita di Roma "Tor Vergata", Via della Ricerca Scienti.ca 1, 00133 Roma, Italy c Dipartimento di Chimica Organica e Industriale and Uniti INSTM, Parco Area delle Scienze 17/A, 43100 Parma, Italy d Dipartimento di Fisica and Unita INFM, Universita di Parma, Parco Area delle Scienze 17/A, 43100 Parma, Italy e Dipartimento di Ingegneria Elettronica, Universita di Roma, "Tor Vergata", 00133 Roma, Italy

We have studied the optical anisotropy of Langmuir-Schaefer layers of PdC10OAP porphyrin, deposited onto gold substrates with thickness in the range 0-16 monolayers (ML). Deposition has been carried out at two values of the surface pressure π, corresponding to different layer structures. In one case (π = 30 mN/m), molecules are well ordered in stacks oriented edge-on with respect to the substrate. In the other (π = 10 mN/m), a complex reorganization of the system happens several days after deposition, to form a mesoscopic two-dimensional lattice. The spectra measured by re.ectance anisotropy spectroscopy (RAS) in two cases are clearly characterized. In the former, the line shape is dominated by a characteristic, large structure appearing in coincidence with the Soret band of the molecule, the development of which from a "peak-like" to a "derivative-like" appearance occurs at a well-de.ned critical thickness  Θc (8 ML). In the latter, the line shape is always "peak-like". We explain both line shapes in terms of morphological characteristics of the layer, occurring at di.erent thickness values. The present results clearly show the potential of RAS to characterize efficiently the deposition of organic materials, and suggest that in short time it will be used as an in situ and real time spectroscopy, as already done in inorganic growth.