Published December 15, 2014 | Version v1
Journal article

Adsorption induced phase transition in Ti(Pc)2 gas sensing films: A joint AFM-EDXR study

  • 1. ISM-CNR, Area della Ricerca di Tor Vergata, Via Fosso del Cavaliere 100, 00133 Roma (Italy)
  • 2. ISM-CNR, Area di Ricerca di Montelibretti, Via Salaria Km.29.5, 00116 Monterotondo Scalo, Roma (Italy)

Description

The morphological properties of thin metal phthalocyanine films, used as active material in gas sensing devices, are studied. Morphological changes, such as bulk or surface phase transitions, are key phenomena, having a determinant influence on the final properties and stability of the materials and devices. In this work, we successfully prove that joint in-situ atomic force microscopy and Energy Dispersive X-ray Reflectivity can be used, not only to monitor the sensing activity of bi[phthalocyaninato(2-)]titanium(IV) films, but also as a powerful tool to disclose the physical-chemical process beneath the sensing activity. Indeed it is shown that NOx adsorption activates a phase transition in the TiPc2 film, characterized by an oscillating behavior between two metastable states. Such phenomena endure as long as the gas molecules are present, finally evolving into the thermodynamically most stable phase. Fourier transform infrared spectroscopy analysis supports the above conclusions. - Highlights: • The NOx gas/TiPc2 sensing film interaction is investigated in real time. • Simultaneous EDXR/AFM techniques disclose a phase transition in the sensing material. • An oscillating α to β1 phase transition is induced by the presence of NOx molecules. • When the sensing process is concluded, the material turns to the most stable phase

Availability note (English)

Available from http://dx.doi.org/10.1016/j.matchemphys.2014.09.004

Additional details

Identifiers

DOI
10.1016/j.matchemphys.2014.09.004;
PII
S0254-0584(14)00586-0;

Publishing Information

Journal Title
Materials Chemistry and Physics
Journal Volume
148
Journal Issue
3
Journal Page Range
p. 949-955
ISSN
0254-0584
CODEN
MCHPDR

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.