Quantum chemical insights into the dissociation of nitric acid on the surface of aqueous electrolytes

Abstract

Recent experiments in our laboratory have shown that the probability of gaseous HNO_3 deprotonation on the surface of water is dramatically enhanced by anions. Herein, we report a quantum chemical study of how a HNO_3 molecule transfers its proton upon approaching water clusters containing or not a chloride ion. We find that HNO_3 always binds to the outermost water molecules both via donating and accepting hydrogen-bonds, but the free energy barrier for subsequent proton transfer into the clusters is greatly reduced in the presence of Cl^−. As the dissociation of HNO_3 embedded in water clusters is barrierless, we infer that interfacial proton transfer to water is hindered by the cost of creating a cavity for NO_(3)^−. Our findings suggest that nearby anions catalyze HNO_3 dissociation by preorganizing interfacial water and drawing the proton—away from the incipient [H^(+)---NO_(3)^−] close ion-pairs generated at the interface. This catalytic mechanism would operate in the 1 mM Cl^− range (1 Cl− in ∼5.5 × 10^4 water molecules) covered by our experiments if weakly adsorbed HNO_3 were able to explore extended surface domains before desorbing or diffusing (undissociated) into bulk water.

Group Members

William A. Goddard III

Charles and Mary Ferkel Professor