<?xml version="1.0" encoding="UTF-8" ?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-14T14:37:22Z</responseDate><request identifier="10.35097/1858" metadataPrefix="oai_dc" verb="GetRecord">https://www.radar-service.eu/oai/OAIHandler</request><GetRecord><record><header><identifier>10.35097/1858</identifier><datestamp>2026-10-09T10:48:40Z</datestamp><setSpec>radar4kit</setSpec></header><metadata><oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/"
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   <dc:identifier>https://dx.doi.org/10.35097/1858</dc:identifier>
   <dc:creator>Fu, Qiang</dc:creator>
   <dc:creator>Wu, Xiaoyu</dc:creator>
   <dc:creator>Luo, Xianlin</dc:creator>
   <dc:creator>Ding, Ziming</dc:creator>
   <dc:creator>Indris, Sylvio</dc:creator>
   <dc:creator>Sarapulova, Angelina</dc:creator>
   <dc:creator>Meng, Zhen</dc:creator>
   <dc:creator>Desmau, Morgane</dc:creator>
   <dc:creator>Wang, Zhengqi</dc:creator>
   <dc:creator>Hua, Weibo</dc:creator>
   <dc:creator>Kübel, Christian K. U.</dc:creator>
   <dc:creator>Schwarz, Björn</dc:creator>
   <dc:creator>Knapp, Michael</dc:creator>
   <dc:creator>Ehrenberg, Helmut</dc:creator>
   <dc:creator>Wei, Yingjin</dc:creator>
   <dc:creator>Dsoke, Sonia</dc:creator>
   <dc:title>Ca2+ Pre-Intercalated Bilayered Vanadium Oxide for High-Performance Aqueous Mg-Ion Batteries</dc:title>
   <dc:publisher>Karlsruhe Institute of Technology</dc:publisher>
   <dc:date>2024</dc:date>
   <dc:subject>Engineering</dc:subject>
   <dc:type>dataset</dc:type>
   <dc:subject>Dataset</dc:subject>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode</dc:rights>
   <dc:description>The “oxygen-rich” Ca2+ pre-intercalated bilayered vanadium oxide (CaVOnH) was synthesized via hydrothermal method and determined as a monoclinic structure with reasonable lattice parameters. CaVOnH achieves a first discharge capacity of 273 mAh g−1 with capacity retention of 91% at 50 mA g−1 in 0.8 m Mg(TFSI)2-85%PEG-15%H2O (polyethylene glycol, PEG), but limited rate capability due to the low ionic conductivity of electrolyte. Dimethyl sulfoxide (DMSO) is used as a co-solvent to tune the physical-chemical properties of aqueous Mg-ion electrolyte (AME), resulting in the reorganization of Mg2+ solvation and hydrogen bond network. The AME containing DMSO shows improved ionic conductivity, low viscosity, and high Mg2+ diffusion coefficient and allows CaVOnH and V2O5 to achieve a much-improved rate capability and capacity. Moreover, the reaction mechanism and reversibility of CaVOnH are elucidated by combining in operando and ex situ techniques. The results demonstrate that CaVOnH undergoes 2-phase reaction and solid solution, the variation of oxidation state and the local environment of vanadium, and reversible formation/decomposition of MgF2 cathode electrolyte interface during Mg2+ (de)intercalation, where MgF2 originated from the decomposition of TFSI-.</dc:description>
   <dc:description>The data include electrochemistry data, XRD, XPS, XAS, and magnetic data, which was plotting using Origin software.&#xD;
The emd. file can be opened and proceeded with Velox software.&#xD;
The dm4. file can be opened and proceeded with DigitalMicrograph software.</dc:description>
   <dc:subject>Aqueous Mg-ion batteries</dc:subject>
   <dc:subject>vanadium oxide cathode</dc:subject>
   <dc:subject>aqueous Mg-ion electrolyte</dc:subject>
   <dc:subject>in operando synchrotron diffraction</dc:subject>
   <dc:subject>in operando X‑ray absorption spectroscopy</dc:subject>
   <dc:format>application/x-tar</dc:format>
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