摘要： Plasmonic aluminum nanoparticles have emerged as an exciting new materials platform due to the high natural abundance of aluminum, their ability to be synthesized in the solution phase, and the potential of these materials to be used for photocatalysis and sensing. However, the photothermal properties of solution-processed aluminum nanoparticles, in particular, how phonon energy transfer depends on the particle size and surface properties, are critical for practical applications and are currently unexplored. Here we use transient absorption spectroscopy, in combination with simulations of phonon and thermal energy dissipation, to investigate the photoresponses of aluminum nanoparticles of various diameters (54, 85, 121, and 144 nm) suspended in 2-propanol. Fast thermal-transfer rates to the solvent (170?280 ps) are observed for particles of all sizes and are facilitated by native oxide coverage, as veri?ed by a two-interface thermal energy-transfer model. Size-dependent phonon “breathing”/vibrational modes are also observed as oscillations in the total cross-section. We ?nd that both the oscillation frequency and the damping rate increase as the diameter of the particles decreases. On the basis of the results of ?nite element calculations, we attribute the damping strength and oscillation period observed to a combination of the noncrystalline nature of the native oxide shell and the presence of surface-bound ligands, both of which increase the vibrational mode damping rates relative to bare Al and Al particles with a bare crystalline oxide shell. These insights should guide future work on controlling energy transfer through the use of size and surface tuning in sustainable aluminum nanomaterial systems for applications in catalysis and sensing.