posted on 2015-07-09, 00:00authored byGuido Soliveri, Valentina Pifferi, Rita Annunziata, Luca Rimoldi, Valentina Aina, Giuseppina Cerrato, Luigi Falciola, Giuseppe Cappelletti, Daniela Meroni
The vapor-phase deposition of triethoxy(octyl)silane
and 1H,1H,2H,2H-perfluoroctyltriethoxysilane on silica substrates was
studied at
different temperatures (70–150 °C). An original combination
of spectroscopic (13C and 29Si solid state NMR,
FTIR), electrochemical (CV, EIS), and surface (surface free energy
determinations, AFM) characterization techniques was adopted to shed
light on the role played by the alkylsilane structure and deposition
temperature on the resulting layer. As for the unfluorinated molecule,
both wettability and ion permeability displayed a bell-shaped curve
with respect to the functionalization temperature. Spectroscopic techniques
showed similar trends in the functionalization degree and suggested
the formation of oligomers/polymers covalently attached to the surface. 29Si NMR proved that higher functionalization temperatures
increase lateral polymerization across the alkylsilane layer. Conversely,
the wettability was almost invariant with the functionalization temperature
for the fluorinated analogue. However, electrochemical and spectroscopic
results had a significant dependence on the functionalization conditions,
even more marked than for the unfluorinated alkylsilane. The higher
thermal reactivity of fluorinated molecules led to vertical polymerization,
as supported by very high water contact angles, diffusion components
in EIS, and a lower degree of covalent bonding with the surface. Optimal
deposition conditions were identified at 100 and 90 °C for the
unfluorinated and fluorinated alkylsilane, respectively.