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

Authors

  • Himanshu Mishra,

    1. Department of Materials Science, California Institute of Technology, California 91125
    2. Materials and Process Simulation Center, California Institute of Technology, California 91125
    3. Ronald and Maxine Linde Center for Global Environmental Science, California Institute of Technology, California 91125
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  • Robert J. Nielsen,

    1. Materials and Process Simulation Center, California Institute of Technology, California 91125
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  • Shinichi Enami,

    1. The Hakubi Center, Kyoto University, Kyoto 606-8302, Japan
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  • Michael R. Hoffmann,

    1. Ronald and Maxine Linde Center for Global Environmental Science, California Institute of Technology, California 91125
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  • Agustín J. Colussi,

    1. Ronald and Maxine Linde Center for Global Environmental Science, California Institute of Technology, California 91125
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  • William A. Goddard III

    Corresponding author
    1. Department of Materials Science, California Institute of Technology, California 91125
    2. Materials and Process Simulation Center, California Institute of Technology, California 91125
    • Department of Materials Science, California Institute of Technology, California 91125
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Abstract

Recent experiments in our laboratory have shown that the probability of gaseous HNO3 deprotonation on the surface of water is dramatically enhanced by anions. Herein, we report a quantum chemical study of how a HNO3 molecule transfers its proton upon approaching water clusters containing or not a chloride ion. We find that HNO3 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 HNO3 embedded in water clusters is barrierless, we infer that interfacial proton transfer to water is hindered by the cost of creating a cavity for NO3. Our findings suggest that nearby anions catalyze HNO3 dissociation by preorganizing interfacial water and drawing the proton—away from the incipient [H+---NO3] close ion-pairs generated at the interface. This catalytic mechanism would operate in the 1 mM Cl range (1 Cl in ∼5.5 × 104 water molecules) covered by our experiments if weakly adsorbed HNO3 were able to explore extended surface domains before desorbing or diffusing (undissociated) into bulk water. © 2012 Wiley Periodicals, Inc.

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