RbCl和CsCl水溶液结构的X射线散射及经验势结构精修模拟（英文）  

Structure of Aqueous RbCl and CsCl Solutions Using X-Ray Scattering and Empirical Potential Structure Refinement Modelling

作　　者：周永全[1] 曾我良枝 山口敏男 房艳[1] 房春晖[1] ZHOU Yongquan;SOGA Yoshie;YAMAGUCHI Toshio;FANG Yan;FANG Chunhui(Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, Qinghai Province, P. R. China;Department of Chemistry, Faculty of Science, Fukuoka University, 8-19-1 Nanakuma, Jonah, Fukuoka 814-0180, Japan)

机构地区：[1]中国科学院青海盐湖研究所,青海西宁810008 [2]福冈大学理学院化学系

出　　处：《物理化学学报》2018年第5期483-491,共9页Acta Physico-Chimica Sinica

基　　金：supported by the Natural Science Foundation of Qinghai Province,China(2015-ZJ-945Q);Youth Innovation Promotion Association,CAS,China(2017467)~~

摘　　要：采用X射线散射法研究了Rb Cl和Cs Cl水溶液的结构,利用基于经验势的结构精修(EPSR)方法获得了溶液中的水合Cl^-、Rb^+、Cs^+、离子缔合及本体水的对径向分布函数、配位数分布及空间密度分布(3D结构)等结构信息。在水溶液中,Cl^-具有相对稳定的6水合结构,其水合距离为0.321 nm,外加阳离子对其水合作用的影响不明显。7.3±1.4个水分子与Rb^+水合,其特征水合距离为0.297 nm,8.4±1.6个水分子与Cs^+水合其水合距离为0.312 nm。Cs^+不具有第二水合层,而Rb^+表现出了更强的水合能力,具有较明显的第二水合层。Cl^-、Rb^+及Cs^+常被认为是"结构破坏"型离子。从微观角度来看这种所谓的"结构破坏"主要体现在破坏了本体水分子的第二水合层保持四面体构型的趋势。Rb Cl和Cs Cl水溶液中部分存在着Rb-Cl和Cs-Cl直接接触离子对,在1.0 mol·dm^(-3)的溶液中Rb–Cl及Cs–Cl的特征距离分别为0.324和0.336nm,溶剂分割离子对的距离则都在0.6 nm左右。相对于Cs^+,Rb^+与Cl^-离子之间表现出了更强的缔合能力。X-ray scattering measurements were performed on 1.0 mol·dm^-3 RbCl and CsCl aqueous solutions. The X-ray structure factors were subjected to empirical potential structure refinement to extract detailed structural information on hydrated Cl^-, Rb^＋, Cs^＋, and ion association, as well as bulk water, in terms of the individual site-site pair correlation functions, coordination number distributions, and spatial density functions （three-dimensional structure）. Cl^- is found to have a relatively stable six-fold coordination of water molecules with a Cl^--H2O distance of 0.321 nm, and without a significant cation effect on its local structure. Rb＋ is surrounded on an average by 7.3 ± 1.4 water molecules with a Rb^＋-H2O distance of 0.297 nm, whereas 8.4 ± 1.6 water molecules hydrate Cs＋ at a Cs^＋-H2O distance of 0.312 nm. It is likely that Rb^＋ has a stronger hydration shell than Cs＋, as evidenced by the presence of the second hydration shell of the former. Contact ion-pairs are partially formed in both solutions and characterized by the Rb^＋-Cl^- and Cs^＋-Cl^- distances of 0.324 nm and 0.336 nm. The solvent-separated ion pairs for both ions are discernible at around 0.6 nm. Rb^＋ has a stronger electrostatic interaction and hence a relatively stronger ion association with Cl^- than Cs^＋.

关 键 词：RBCL CSCL 溶液结构 X射线散射 EPSR 

分 类 号：O641[理学—物理化学]