| Autor: |
Bondy AL; Department of Chemistry, University of Michigan , Ann Arbor, Michigan 48109, United States., Kirpes RM; Department of Chemistry, University of Michigan , Ann Arbor, Michigan 48109, United States., Merzel RL; Department of Chemistry, University of Michigan , Ann Arbor, Michigan 48109, United States., Pratt KA; Department of Chemistry, University of Michigan , Ann Arbor, Michigan 48109, United States., Banaszak Holl MM; Department of Chemistry, University of Michigan , Ann Arbor, Michigan 48109, United States., Ault AP; Department of Chemistry, University of Michigan , Ann Arbor, Michigan 48109, United States.; Department of Environmental Health Sciences, University of Michigan , Ann Arbor, Michigan 48109, United States. |
| Abstrakt: |
Chemical analysis of atmospheric aerosols is an analytical challenge, as aerosol particles are complex chemical mixtures that can contain hundreds to thousands of species in attoliter volumes at the most abundant sizes in the atmosphere (∼100 nm). These particles have global impacts on climate and health, but there are few methods available that combine imaging and the detailed molecular information from vibrational spectroscopy for individual particles <500 nm. Herein, we show the first application of atomic force microscopy with infrared spectroscopy (AFM-IR) to detect trace organic and inorganic species and probe intraparticle chemical variation in individual particles down to 150 nm. By detecting photothermal expansion at frequencies where particle species absorb IR photons from a tunable laser, AFM-IR can study particles smaller than the optical diffraction limit. Combining strengths of AFM (ambient pressure, height, morphology, and phase measurements) with photothermal IR spectroscopy, the potential of AFM-IR is shown for a diverse set of single-component particles, liquid-liquid phase separated particles (core-shell morphology), and ambient atmospheric particles. The spectra from atmospheric model systems (ammonium sulfate, sodium nitrate, succinic acid, and sucrose) had clearly identifiable features that correlate with absorption frequencies for infrared-active modes. Additionally, molecular information was obtained with <100 nm spatial resolution for phase separated particles with a ∼150 nm shell and 300 nm core. The subdiffraction limit capability of AFM-IR has the potential to advance understanding of particle impacts on climate and health by improving analytical capabilities to study water uptake, heterogeneous reactivity, and viscosity. |
