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Reductive transformation of V(III) precursors into vanadium(II) oxide nanowires

机译:V(III)前体的还原转化为钒(II)氧化物纳米线

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摘要

Vanadium(II) oxide nanostructures are promising materials for supercapacitors and electrocatalysis because of their excellent electrochemical properties and high surface area. In this study, new homoleptic vanadium(III) complexes with bi-dentate O,N-chelating heteroarylalkenol ligands (DmoxCH=COCF3, PyCH=COCF3 and PyN=COCF3) were synthesized and successfully transformed by reductive conversion into VO nanowires. The chemical identity of V(iii) complexes and their redox behaviour were unambiguously established by single crystal X-ray diffraction studies, cyclic voltammetry, spectrometric studies and DFT calculations. Transformation into the metastable VO phase was verified by powder X-ray diffraction and thermo-gravimetry. Transmission electron microscopy and X-ray photoelectron spectroscopy data confirmed the morphology and chemical composition of VO nanostructures, respectively.
机译:钒(II)氧化物纳米结构是超级电容器和电常分的有希望的材料,因为它们优异的电化学性能和高表面积。 在该研究中,合成并通过将转化转化为VO纳米线,合成并成功地合成了具有双齿型o,n螯合杂芳基烯醇配体(Dmoxch = Cocff3,Pyn = Cocf3和Pyn = Cocf3)的新型钒(III)复合物。 通过单晶X射线衍射研究,循环伏安法,光谱研究和DFT计算,V(III)复合物的化学特性及其氧化还原行为明确地建立了明确建立的。 通过粉末X射线衍射和热重量验证转化到亚稳态VO相。 透射电子显微镜和X射线光电子能谱数据分别证实了VO纳米结构的形态和化学组成。

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