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首页> 外文期刊>The Journal of Chemical Physics >Electron solvation in water-ammonia mixed clusters;Structure,energetics,and the nature of localization states of the excess electron
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Electron solvation in water-ammonia mixed clusters;Structure,energetics,and the nature of localization states of the excess electron

机译:水氨混合团簇中的电子溶剂化;结构,能量和过量电子的局域态性质

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The structure and energetics of water-ammonia mixed clusters with an excess electron,[(H2O)n(NH3)_m]~-with m=1,n=2-6 and m=2,n=2,and also the corresponding neutral clusters are investigated in detail by means of ab initio quantum chemical calculations.The authors focus on the localization structure of the excess electron with respect to its surface versus interiorlike states,its binding to ammonia versus water molecules,the spatial and orientational arrangement of solvent molecules around the excess electron,the changes of the overall hydrogen-bonded structure of the clusters as compared to those of the neutral ones and associated dipole moment changes,vertical detachment energies of the anionic clusters,and also the vertical attachment energies of the neutral clusters.It is found that the hydrogen-bonded structure of the anionic clusters are very different from those of the neutral clusters unlike the case of water-ammonia dimer anion,and these changes in structural arrangements lead to drastically different dipole moments of the anionic and the neutral clusters.The spatial distribution of the singly occupied molecular orbital holding the excess electron shows only surface states for the smaller clusters.However,for n=5 and 6,both surface and interiorlike binding states are found to exist for the excess electron.For the surface states,the excess electron can be bound to the dangling hydrogens of either an ammonia or a water molecule with different degrees of stability and vertical detachment energies.The interiorlike states,wherever they exist,are found to have a higher vertical detachment energy than any of the surface states of the same cluster.Also,for interiorlike states,the ammonia molecule with its dangling hydrogens is always found to stay on top or on a far side of the charge density of the excess electron without participating in the hydrogen bond network of the cluster;the intermolecular hydrogen bonds are formed by the water molecules only which add to the overall stability of these anionic clusters.
机译:电子[[H2O] n(NH3)_m]〜-(m = 1,n = 2-6和m = 2,n = 2)以及具有相应电子的水氨混合团簇的结构和能量通过从头算量子化学计算来详细研究中性团簇。作者着重研究了过量电子相对于其表面状态与内部状态的局部结构,其与氨水分子的结合,溶剂的空间和方向排列多余电子周围的分子,团簇的整体氢键结构与中性团簇相比的变化以及相关的偶极矩变化,阴离子团簇的垂直脱离能以及中性团簇的垂直附着能。发现与水-氨二聚体阴离子的情况不同,阴离子簇的氢键结构与中性簇的氢键结构有很大的不同,这些结构上的变化导致阴离子和中性团簇的偶极矩完全不同。持有过量电子的单占据分子轨道的空间分布仅显示较小团簇的表面状态。但是,对于n = 5和6,表面和内部类似的结合状态对于表面态,多余的电子可以与具有不同程度的稳定性和垂直脱离能的氨或水分子的悬空氢结合。被发现具有比相同簇的任何表面态更高的垂直脱离能。此外,对于内部类态,总是会发现带有悬挂氢的氨分子始终位于其电荷密度的顶部或远端。多余的电子不参与团簇的氢键网络;分子间的氢键仅由水分子形成这些阴离子簇的整体稳定性。

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