Lim Sung-Chul, Lee Jinhee, Kwak Hunho H, Heo Jongwook W, Chae Munseok S, Ahn Docheon, Jang Yun Hee, Lee Hochun, Hong Seung-Tae
Department of Energy Systems Engineering, DGIST (Daegu Gyeongbuk Institute of Science & Technology) , Daegu 42988, South Korea.
Pohang Accelerator Laboratory , Pohang 37673, South Korea.
Inorg Chem. 2017 Jul 17;56(14):7668-7678. doi: 10.1021/acs.inorgchem.7b00204. Epub 2017 Jun 24.
Magnesium batteries have received attention as a type of post-lithium-ion battery because of their potential advantages in cost and capacity. Among the host candidates for magnesium batteries, orthorhombic α-VO is one of the most studied materials, and it shows a reversible magnesium intercalation with a high capacity especially in a wet organic electrolyte. Studies by several groups during the last two decades have demonstrated that water plays some important roles in getting higher capacity. Very recently, proton intercalation was evidenced mainly using nuclear resonance spectroscopy. Nonetheless, the chemical species inserted into the host structure during the reduction reaction are still unclear (i.e., Mg(HO), Mg(solvent, HO), H, HO, HO, or any combination of these). To characterize the intercalated phase, the crystal structure of the magnesium-inserted phase of α-VO, electrochemically reduced in 0.5 M Mg(ClO) + 2.0 M HO in acetonitrile, was solved for the first time by the ab initio method using powder synchrotron X-ray diffraction data. The structure was tripled along the b-axis from that of the pristine VO structure. No appreciable densities of elements were observed other than vanadium and oxygen atoms in the electron density maps, suggesting that the inserted species have very low occupancies in the three large cavity sites of the structure. Examination of the interatomic distances around the cavity sites suggested that HO, HO, or solvated magnesium ions are too big for the cavities, leading us to confirm that the intercalated species are single Mg ions or protons. The general formula of magnesium-inserted VO is MgHVO, (0.66 ≤ x ≤ 1.16). Finally, density functional theory calculations were carried out to locate the most plausible atomic sites of the magnesium and protons, enabling us to complete the structure modeling. This work provides an explicit answer to the question about Mg intercalation into α-VO.
镁电池作为一种锂离子后电池受到了关注,因为它们在成本和容量方面具有潜在优势。在镁电池的主体候选材料中,正交晶系的α-VO是研究最多的材料之一,它在湿有机电解质中表现出高容量的可逆镁嵌入。过去二十年中,几个研究小组的研究表明,水在获得更高容量方面起着重要作用。最近,主要通过核磁共振光谱证实了质子嵌入。然而,还原反应过程中插入主体结构的化学物种仍不清楚(即Mg(HO)、Mg(溶剂,HO)、H、HO、HO或它们的任何组合)。为了表征嵌入相,首次使用粉末同步加速器X射线衍射数据,通过从头算方法解析了在乙腈中0.5 M Mg(ClO) + 2.0 M HO中电化学还原的α-VO镁嵌入相的晶体结构。该结构沿b轴比原始VO结构增大了两倍。在电子密度图中,除了钒和氧原子外,未观察到明显的元素密度,这表明插入物种在结构的三个大空洞位置中的占有率非常低。对空洞位置周围原子间距离的检查表明,HO、HO或溶剂化镁离子对于空洞来说太大,这使我们确认嵌入物种是单个Mg离子或质子。镁嵌入VO的通式为MgHVO,(0.66 ≤ x ≤ 1.16)。最后,进行了密度泛函理论计算,以确定镁和质子最合理的原子位置,从而完成结构建模。这项工作为关于Mg嵌入α-VO的问题提供了明确答案。