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Structure of hydrated cobalt ions confined in the nanospace of single-walled carbon nanotubes

机译:局限在单壁碳纳米管纳米空间中的水合钴离子的结构

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The structure of hydrated Co ions confined in the nanospace of single-walled carbon nanotubes (SWNTs) has been studied using the X-ray absorption fine structure (XAFS) technique. Water adsorption isotherms on Co-impregnated SWNTs indicate a high affinity of Co ions to water molecules. The results of XAFS analysis provided the information on the proportion of dissolved species in nanospaces against the total amount of cobalt ions adsorbed on the open-pored SWNT. The structural information of the first shell around a Co ion was expressed in terms of the hydration number, Co-0 distance and Debye-Waller factor. The actual coordination number and the interatomic distance of Co-0 for the dissolved species were remarkably reduced compared to the bulk aqueous solution indicating the dehydration of water molecules from Co ions and a compact hydrated structure in the micropore of SWNTs.
机译:利用X射线吸收精细结构(XAFS)技术研究了局限在单壁碳纳米管(SWNTs)纳米空间中的水合Co离子的结构。共浸渍的SWNT上的水吸附等温线表明Co离子对水分子的亲和力高。 XAFS分析的结果提供了有关纳米空间中溶解的物种相对于在开放式SWNT上吸附的钴离子总量的比例的信息。 Co离子周围第一个壳的结构信息以水合数,Co-0距离和Debye-Waller因子表示。与本体水溶液相比,溶解态物质的实际配位数和Co-0的原子间距离显着降低,表明水分子从Co离子中脱水,并在SWNTs的微孔中形成紧密的水合结构。

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