Accurate calculation of the ion-ion recombination rate coefficient has been of longstanding interest, as it controls the ion concentration in gas phase systems and in aerosols. We describe the development of a hybrid continuum-molecular dynamics approach to determine the ion-ion recombination rate coefficient. The approach is based on the limiting sphere method classically used for transition regime collision phenomena in aerosols. When ions are sufficiently far from one another, ion-ion relative motion is described by diffusion equations while within a critical distance, molecular dynamics (MD) simulations are used to model ion-ion motion. MD simulations are parameterized using the AMBER force-field as well as by considering partial charges on atoms. Ion-neutral gas collisions are modeled in two mutually exclusive cubic domains composed of 10 3 gas atoms each, which remain centered on the recombining ions throughout calculations. Example calculations are reported for NH 4 + recombination with NO 2 in He, across a pressure range from 10 kPa to 10,000 kPa. Excellent agreement is found in comparison of calculations to literature values for the 100 kPa recombination rate coefficient (1.0 x 10 -12 m 3 s -1 ) in He. We also recover the experimentally observed increase in recombination rate coefficient with pressure at sub-atmospheric pressures, and the observed decrease in recombination rate coefficient in the high pressure continuum limit. We additionally find that non-dimensionalized forms of rate coefficients are consistent with recently developed equations for the dimensionless charged particle-ion collision rate coefficient based on Langevin dynamics simulations.

Simultaneous gas-phase hydrogen/deuterium exchange and ion-neutral clustering are monitored in an atmospheric pressure drift cell to quantify the effects of vapor association on observed rates of deuterium incorporation for select amino acids.

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The charge reduction of multiply charged macromolecular ions via recombination with small ions in the gas phase is commonly employed to modulate the charge on macromolecules prior to mass spectrometric...