Unusual Interfacial Freezing
Phenomena in Hexacontane/Silica Composites
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Abstract
The
crystallization behaviors of <i>n-</i>hexacontane (C<sub>60</sub>H<sub>122</sub>)/Stöber silica (SiO<sub>2</sub>) composites
with various compositions were investigated by a combination of differential
scanning calorimetry (DSC), solid-state <sup>13</sup>C nuclear magnetic
resonance (solid-state <sup>13</sup>C NMR), and proton NMR relaxation
experiments. By means of DSC, C<sub>60</sub>H<sub>122</sub> molecules
in C<sub>60</sub>H<sub>122</sub>/silica composites were observed to
be involved in the interfacial freezing not present in the free bulk
C<sub>60</sub>H<sub>122</sub>. The orientation of C<sub>60</sub>H<sub>122</sub> molecules, being preferentially normal to silica surface,
was confirmed by grazing incidence X-ray diffraction experiments on
thin <i>n-</i>hexacontane film adsorbed on the silicon wafer
with a native SiO<sub>2</sub> layer. Inferred from the solid <sup>13</sup>C NMR data, the interfacial monolayer is in orthorhombic
phase with certain chain disorders. It is speculated that the “interfacial
freezing” of C<sub>60</sub>H<sub>122</sub> formed in the presence
of silica particles is driven by the combination of the strong attraction
between the molecules and the enhanced number of interfacial molecules
on the silica surface