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氧化还原惰性离子控制着分子态钒氧化物的氧化还原活性。

Redox-inactive ions control the redox-activity of molecular vanadium oxides.

作者信息

Greiner Simon, Schwarz Benjamin, Ringenberg Mark, Dürr Maximilian, Ivanovic-Burmazovic Ivana, Fichtner Maximilian, Anjass Montaha, Streb Carsten

机构信息

Institute of Inorganic Chemistry I, Ulm University Albert-Einstein-Allee 11 89081 Ulm Germany

Helmholtz Institute Ulm for Electrochemical Energy Storage (HIU) Helmholtzstr. 11 89081 Ulm Germany.

出版信息

Chem Sci. 2020 Apr 6;11(17):4450-4455. doi: 10.1039/d0sc01401j.

Abstract

Polyoxometalates are key materials for energy conversion and storage due to their unique chemical tunability and electrochemical reactivity. Herein, we report that functionalization of molecular vanadium oxides, polyoxovanadates, with redox-inert Ca cations leads to a significant increase in their electron storage capabilities. The electrochemical performance of the Ca-functionalized dodecavanadate [CaVOCl(DMF)] (= ) was thus compared with that of the precursor compound (HNMe)[VOCl] (= ). can store up to five electrons per cluster, while only shows one reversible redox transition. In initial studies, we demonstrated that can be used as an active material in lithium-ion cathodes. Our results show how redox-inert cations can be used as structural and electrostatic stabilizers, leading to major changes in the redox-chemistry of polyoxovanadates.

摘要

多金属氧酸盐因其独特的化学可调性和电化学反应性,是能量转换和存储的关键材料。在此,我们报告了用氧化还原惰性的Ca阳离子对分子钒氧化物(多钒酸盐)进行功能化,会使其电子存储能力显著提高。因此,将钙功能化的十二钒酸盐[CaVOCl(DMF)](= )的电化学性能与前体化合物(HNMe)[VOCl](= )进行了比较。 每个簇最多可存储五个电子,而 仅显示一个可逆的氧化还原转变。在初步研究中,我们证明了 可以用作锂离子阴极中的活性材料。我们的结果表明氧化还原惰性阳离子如何用作结构和静电稳定剂,从而导致多钒酸盐氧化还原化学的重大变化。

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