Unraveling the Magnesium-Ion Intercalation Mechanism in Vanadium Pentoxide in a Wet Organic Electrolyte by Structural Determination

被引:63
作者
Lim, Sung-Chul [1 ]
Lee, Jinhee [1 ]
Kwak, Hunho H. [1 ]
Heo, Jongwook W. [1 ]
Chae, Munseok S. [1 ]
Ahn, Docheon [2 ]
Jang, Yun Hee [1 ]
Lee, Hochun [1 ]
Hong, Seung-Tae [1 ]
机构
[1] DGIST, Dept Energy Syst Engn, Daegu 42988, South Korea
[2] Pohang Accelerator Lab, Pohang 37673, South Korea
基金
新加坡国家研究基金会;
关键词
BOND-VALENCE PARAMETERS; CATHODE-ACTIVE MATERIAL; ELECTROCHEMICAL INSERTION; CRYSTAL-STRUCTURE; MG; LITHIUM; OXIDES; BATTERY; PROGRAM; ENERGY;
D O I
10.1021/acs.inorgchem.7b00204
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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 alpha-V2O5 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(H2O)(2), Mg(solvent, H2O)(n)(2+), H3O+, H2O, or any combination of these). To characterize the intercalated phase, the crystal structure of the magnesium-inserted phase of alpha-V2O5, electrochemically reduced in 0.5 M Mg(ClO4)(2) + 2.0 M H2O 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 V2O5 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 H2O, H3O+, or solvated magnesium ions are too big for the cavities, leading us to confirm that the intercalated species are single Mg2+ ions or protons. The general formula of magnesium-inserted V2O5 is Mg0.17HxV2O5, (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 alpha-V2O5.
引用
收藏
页码:7668 / 7678
页数:11
相关论文
共 76 条
  • [11] BOND-VALENCE PARAMETERS OBTAINED FROM A SYSTEMATIC ANALYSIS OF THE INORGANIC CRYSTAL-STRUCTURE DATABASE[J]. BROWN, ID;ALTERMATT, D. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1985(AUG)
  • [12] VALENCE: A program for calculating bond valences[J]. Brown, ID. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1996
  • [13] Nanomaterials for rechargeable lithium batteries[J]. Bruce, Peter G.;Scrosati, Bruno;Tarascon, Jean-Marie. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008(16)
  • [14] THE LIXV2O5 SYSTEM - AN OVERVIEW OF THE STRUCTURE MODIFICATIONS INDUCED BY THE LITHIUM INTERCALATION[J]. DELMAS, C;COGNACAURADOU, H;COCCIANTELLI, JM;MENETRIER, M;DOUMERC, JP. SOLID STATE IONICS, 1994(3-4)
  • [15] A REFINEMENT OF THE STRUCTURE OF V2O5[J]. ENJALBERT, R;GALY, J. ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 1986
  • [16] THE CRYSTAL STRUCTURES OF 3 NEW VANADIUM OXIDE MINERALS[J]. EVANS, HT;MROSE, ME. ACTA CRYSTALLOGRAPHICA, 1958(01)
  • [17] Role of Structural H2O in Intercalation Electrodes: The Case of Mg in Nanocrystalline Xerogel-V2O5[J]. Gautam, Gopalakrishnan Sai;Canepa, Pieremanuele;Richards, William Davidson;Malik, Rahul;Ceder, Gerbrand. NANO LETTERS, 2016(04)
  • [18] Electrochemical and Spectroscopic Analysis of Mg2+ Intercalation into Thin Film Electrodes of Layered Oxides: V2O5 and MoO3[J]. Gershinsky, Gregory;Yoo, Hyun Deog;Gofer, Yosef;Aurbach, Doron. LANGMUIR, 2013(34)
  • [19] A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu[J]. Grimme, Stefan;Antony, Jens;Ehrlich, Stephan;Krieg, Helge. JOURNAL OF CHEMICAL PHYSICS, 2010(15)
  • [20] A new polymorph of VO2 prepared by soft chemical methods[J]. Hagrman, D;Zubieta, J;Warren, CJ;Meyer, LM;Treacy, MMJ;Haushalter, RC. JOURNAL OF SOLID STATE CHEMISTRY, 1998(01)