Greiner Simon, Schwarz Benjamin, Ringenberg Mark, Dürr Maximilian, Ivanovic-Burmazovic Ivana, Fichtner Maximilian, Anjass Montaha, Streb Carsten
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.
Chem Sci. 2020 Apr 6;11(17):4450-4455. doi: 10.1039/d0sc01401j.
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.
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。