Hirshberg Barak, Gerber R Benny
Institute of Chemistry and the Fritz-Haber center for Molecular Dynamics, The Hebrew University , Jerusalem 9190401, Israel.
Department of Chemistry, University of California , Irvine, California 92697, United States.
J Phys Chem Lett. 2016 Aug 4;7(15):2905-9. doi: 10.1021/acs.jpclett.6b01109. Epub 2016 Jul 18.
A new mode of formation is proposed for carbonic acid in the atmosphere. It involves impact of vibrationally excited gas-phase CO2 molecules on water or ice particles. This is a first mechanism that supports formation on ice as well as on liquid water surfaces. Results of ab initio molecular dynamics simulations are presented on collisions of CO2 with (H2O)n clusters (n = 1, 4, 8, 12). Efficient formation of carbonic acid is seen with product lifetimes exceeding 100 ps. The reaction is feasible even for collision of CO2 with a single water molecule but in a different mechanism than for larger clusters. For clusters, the transition state shows charge separation into H3O(+)···HCO3(-), which transforms into neutral carbonic acid as the product, hydrated by the remaining waters. Possible atmospheric implications of the results are discussed.
提出了一种大气中碳酸形成的新模式。它涉及振动激发的气相二氧化碳分子与水或冰粒子的碰撞。这是第一个支持在冰以及液态水表面形成碳酸的机制。给出了二氧化碳与(H₂O)ₙ团簇(n = 1、4、8、12)碰撞的从头算分子动力学模拟结果。观察到碳酸的高效形成,产物寿命超过100皮秒。即使二氧化碳与单个水分子碰撞,该反应也是可行的,但机制与与较大团簇碰撞时不同。对于团簇,过渡态显示电荷分离为H₃O⁺···HCO₃⁻,其转化为中性碳酸产物,并被其余的水所水化。讨论了该结果可能对大气产生的影响。