机械化学合成MgV2O4:由磨矿能和前驱体驱动的反应途径。

IF 4.7 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Anna Michaely,Hong Chen,Oliver Clemens,Maxim Neuberger,Christopher W M Kay,Robert Haberkorn,Guido Kickelbick
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引用次数: 0

摘要

镁尖晶石如MgAl2O4和MgFe2O4已被广泛探索用于储能和传感应用,但MgV2O4仍然相对未被开发,尽管它有很大的潜力,例如作为电池电极材料。在这项研究中,我们报道了第一次在室温下用MgO或Mg与各种钒氧化物作为反应物机械化学合成MgV2O4。在DFT水平的热力学计算指导下,只有V2O5和Mg之间的自维持反应在铣削20分钟内导致MgV2O4,以及MgO作为副产物。随着转速的增加,在铣削几分钟后,反应开始提前,纳米范围内的晶粒尺寸变小,MgV2O4的应变增加。此外,x射线衍射和电子顺磁共振测量结果表明,苛刻的磨矿条件会导致两相的非化学计量增加,从而形成富镁尖晶石和含钒岩盐相。合成后的酸洗除去了MgO,电化学阻抗谱分析表明,较温和的研磨条件由于缺陷数量较少而提高了MgV2O4的电导率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanochemical Synthesis of MgV2O4: Reactivity Pathways Driven by Milling Energy and Precursors.
Magnesium spinels such as MgAl2O4 and MgFe2O4 have been widely explored for energy storage and sensing applications, but MgV2O4 remains relatively unexplored despite its promising potential, e.g., as a battery electrode material. In this study, we report the first mechanochemical synthesis of MgV2O4 at room temperature using either MgO or Mg with various vanadium oxides as reactants. Directed by thermodynamic calculations on a DFT level, only the self-sustaining reaction between V2O5 and Mg led to MgV2O4 within 20 min of milling, along with MgO as a side product. With increasing rotational speed, an earlier reaction ignition after a few minutes of milling, smaller crystallite sizes in the nanometer range, and increased strain in MgV2O4 were observed. In addition, harsh milling conditions induce increasing nonstoichiometry in both phases, leading to a magnesium-rich spinel and a vanadium-containing rock salt phase, as supported by X-ray diffraction and electron paramagnetic resonance measurements. Acid washing after synthesis removed MgO, and electrochemical impedance spectroscopy showed that milder grinding conditions increased the conductivity of MgV2O4 due to the smaller number of defects.
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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