摘要： Water at interfaces is considered present and important within almost all physical processes. Interfacial water shows nonbulk properties, however, its structure/organization and dynamics are on a still open debate. In parallel to that, the interfacial polymer in nanocomposites exhibits modi?ed structure and dynamics, the latter characteristic being widely considered responsible for the improved nanocomposite properties. One of the most suitable tools for studying dynamics of a variety of small molecules and macromolecules is broadband dielectric spectroscopy (BDS), mainly due to its high resolving power. BDS is employed here in combination with isothermal hydration and has proved quite illuminating in recording for the ?rst time striking similarities in the dynamics behavior between water molecules and ?exible polydimethylsiloxane macromolecules, when the latter molecules are individually adsorbed physically on the attractive surfaces of metal oxide nanoparticle. The qualitative similarities between water and polymer interfacial dynamics, for example, in their exhibiting time-scale and the elevation of the respective activation energy upon increasing of interfacial molecules fraction, lay most probably at the origins of the same main surface-adsorbed molecule interaction, i.e.. the hydrogen bonding. Whereas, the quantitative di?erences in molecular dynamics, e.g., slower, more energetically demanding, and cooperative interfacial dynamics for the polymer than for water, arise from the di?erent scale of the two molecular motions (<1 nm for water and ≥1 nm for the polymer) and/or from alternations in interfacial layer density.