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From Metal Thiobenzoates to Metal Sulfide Nanocrystals: An Experimental and Theoretical Investigation

机译:从金属硫代苯甲酸盐到金属硫化物纳米晶体的实验和理论研究

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摘要

A simple preparation of metal sulfide nanoparticles via the decomposition of thiobenzoate precursors at room temperature is presented and discussed. Long chain alkylamines were found to mediate the breakdown of metal thiobenzoates, such as those containing Ag, Cu, In and Cd, to produce uniform Ag2S, Cu2−xS, In2S3 and CdS nanoparticles respectively. The long chain amines are assumed to play dual roles as the nucleophilic reagent and the capping agent. It was found that sizes of the nanoparticles can be controlled by changing the type of amine used, as well as the molar ratio between amine and the precursor. We performed DFT calculations on a proposed mechanism involving an initial nucleophilic addition of amine molecule onto the thiocarboxylates. The proposed reaction was also confirmed through the analysis of by-products via infrared spectroscopy. On the basis of this understanding, we propose to manipulate the stability of the precursors by coordination with suitable stabilizing groups, such that the reaction kinetics can be modified to generate different nanostructures of interest.
机译:提出并讨论了通过硫代苯甲酸酯前体在室温下的分解制备金属硫化物纳米粒子的简单方法。发现长链烷基胺介导金属硫代苯甲酸盐的分解,例如含有银,铜,铟和镉的那些,分别产生均匀的Ag2S,Cu2-xS,In2S3和CdS纳米颗粒。假定长链胺起亲核试剂和封端剂的双重作用。已经发现,可以通过改变所用胺的类型以及胺与前体之间的摩尔比来控制纳米颗粒的尺寸。我们对提议的机制进行了DFT计算,该机制涉及将胺分子初始亲核加成到硫代羧酸盐上。通过红外光谱分析副产物也证实了所提出的反应。基于这种理解,我们提议通过与合适的稳定基团配位来操纵前体的稳定性,从而可以修改反应动力学以产生感兴趣的不同纳米结构。

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