Theoretical analysis for photophoresis of a microscale hydrophobic particle in liquids.

In the present study, combining the conventional photothermal analysis and the concept of interaction of solvent molecules in interfacial layer used for thermophoresis in liquid, a theory for photophoresis of a hydrophobic particle suspended in liquids is developed. To characterize hydrophobicity of the micro-particle, slip length in Navier's formula is used as an index. Analytical expressions are derived and a parametric analysis for photophoretic velocity is performed with emphasis on the influences of particle characteristics such as size, optical properties, hydrophobicity, and thermal conductivity. Heat source function and the corresponding asymmetry factor at various conditions are evaluated to interpret the mechanisms of negative and positive photophoresis and the conditions for transition between them. The present theory discloses that the particle surface hydrophobicity or fluid slippage at particle-liquid interface may lead to a remarkable enhancement in the particle photophoretic velocity in liquids. Higher particle thermal conductivity and larger size of liquid molecules both result in weaker photophoretic motion.