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Carbon nanotubes as electrically active nanoreactors for multi-step inorganic synthesis: sequential transformations of molecules to nanoclusters, and nanoclusters to nanoribbons

机译:碳纳米管作为用于多步无机合成的电活性纳米反应器:分子到纳米簇的顺序转换,以及纳米簇到纳米带的顺序转换

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摘要

In organic synthesis, the composition and structure of products are predetermined by the reaction conditions; however, the synthesis of well-defined inorganic nanostructures often presents a significant challenge yielding non-stoichiometric or polymorphic products. In this study, confinement in the nanoscale cavities of single-walled carbon nanotubes (SWNT) provides a new approach for multi-step inorganic synthesis where sequential chemical transformations take place within the same nanotube. In the first step, SWNT donate electrons to the reactant iodine molecules (I2) transforming them to iodide anions (I-). These then react with metal hexacarbonyls (M(CO)6, M = Mo or W) in the next step yielding anionic nanoclusters [M6I14]2-, the size and composition of which are strictly dictated by the nanotube cavity, as demonstrated by aberration corrected high resolution transmission electron microscopy (AC-HRTEM), scanning transmission electron microscopy (STEM) and energy dispersive X-ray (EDX) spectroscopy. Atoms in the nanoclusters [M6I14]2- are arranged in a perfect octahedral geometry and can engage in further chemical reactions within the nanotube, either reacting with each other leading to a new polymeric phase of molybdenum iodide [Mo6I12]n, or with hydrogen sulphide gas giving rise to nanoribbons of molybdenum/tungsten disulphide [MS2]n in the third step of the synthesis. Electron microscopy measurements demonstrate that the products of the multi-step inorganic transformations are precisely controlled by the SWNT nanoreactor, with complementary Raman spectroscopy revealing the remarkable property of SWNT to act as a reservoir of electrons during the chemical transformation. The electron transfer from the host-nanotube to the reacting guest-molecules is essential for stabilising the anionic metal iodide 2 nanoclusters and for their further transformation to metal disulphide nanoribbons synthesised in the nanotubes in high yield.
机译:在有机合成中,产物的组成和结构是由反应条件预先确定的。然而,定义明确的无机纳米结构的合成通常对产生非化学计量或多晶型产物提出了重大挑战。在这项研究中,限制在单壁碳纳米管(SWNT)的纳米级腔中提供了一种新的多步无机合成方法,该方法在同一纳米管内发生顺序化学转化。第一步,SWNT将电子捐赠给反应物碘分子(I2),将其转化为碘化物阴离子(I-)。然后,它们在下一步与金属六羰基化合物(M(CO)6,M = Mo或W)反应,生成阴离子纳米簇[M6I14] 2-,其大小和组成由纳米管腔严格控制,如像差所示校正的高分辨率透射电子显微镜(AC-HRTEM),扫描透射电子显微镜(STEM)和能量色散X射线(EDX)光谱。纳米团簇[M6I14] 2-中的原子排列成完美的八面体几何形状,并且可以在纳米管内参与进一步的化学反应,彼此反应导致碘化钼[Mo6I12] n形成新的聚合相,或者与硫化氢发生反应气体在合成的第三步中产生了纳米带状的钼/二硫化钨[MS2] n。电子显微镜测量表明,多步无机转化的产物由SWNT纳米反应器精确控制,互补拉曼光谱揭示了SWNT在化学转化过程中作为电子储库的显着特性。电子从主体纳米管转移到反应的客体分子对于稳定阴离子金属碘化物2纳米团簇以及将其进一步转化为纳米管中高产率合成的金属二硫化物纳米带至关重要。

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