The surface of nitric acid solutions: Insights gained from a combined experimental and computational approach

COMP 134

Geraldine L. Richmond, richmond@uoregon.edu, Department of Chemistry, University of Oregon, Eugene, OR 97403
Nitric acid plays an important role in the heterogeneous chemistry of the atmosphere. Reactions involving HNO3 at aqueous interfaces in the stratosphere and troposphere depend on the state of nitric acid at these surfaces. This presentation will discuss our recent results involving a combination of vibrational sum frequency spectroscopy (VSFS) and ab-initio calculations to understand the surface of HNO3-H2O binary solutions and HNO3-H2SO4-H2O ternary solutions. Spectra of the NO2 group at different HNO3 mole fractions and under different polarization combinations are used to develop a detailed picture of these atmospherically important systems. Consistent with surface tension and spectroscopic measurements from other laboratories, molecular nitric acid is identified at the surface of concentrated solutions. However, the data here reveal the adsorption of two different hydrogen-bonded species of undissociated HNO3 in the interfacial region that differ in their degree of solvation of the nitro group. The adsorption of these undissociated nitric acid species is shown to be sensitive to the H2O:HNO3 ratio as well as to the concentration of sulfuric acid. The calculations compare well with the experimental results and provide further insights into the interesting interfacial interactions present at these environmentally important nitric acid surfaces.