Depth profiling of heterogeneously mixed aerosol particles using single-particle mass spectrometry.

Abstract

Infrared laser evaporation of single aerosol particles in a vacuum followed by vacuum ultraviolet (VUV) laser ionization and time-of-flight mass spectroscopy of the resulting vapor provides a depth profile of the particle's composition. Analyzing glycerol particles coated with 60-150-nm coatings of oleic acid using either a CO2 laser or a tunable optical parametric oscillator as an evaporation laser results in mass spectra that depend on the IR laser power. Low infrared laser powers incompletely vaporize particles and preferentially probe the composition of the surface layers of the particle, but high laser powers evaporate the entire particle and produce spectra representative of the particle's total composition. In the limit of low laser power, the fraction of oleic acid in the mass spectra is as much as 50 times greater than the fraction of oleic acid in the particle, providing a surface-layer-specific characterization. The OPO laser provides even more surface specificity, producing an [oleic acid]/[glycerol] ratio as much as four times larger (for a 60-nm coating) than that obtained using the CO2 laser. The infrared laser power required to sample the core of the particle increases with the thickness of the coating and is sensitive to changes in the coating thickness on the order of 10 nm. In contrast to these intuitively appealing results, high CO2 laser powers (approximately 90 mJ/pulse) produce mass spectra that, at short delays between the CO2 and VUV lasers, show enrichment of the core material rather than the coating. Likewise, tuning the OPO to frequencies that are resonant with the core material but transparent to the coating also results in selective detection of the core. The results suggest that a shattering mechanism dominates the vaporization dynamics in these situations.