Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Na + preintercalated bilayered vanadium oxide (NVOnH) with a large interlayer spacing of ∼11.1 Å is synthesized via a hydrothermal method. As proven by mass spectrometry and magnetization measurements, NVOnH is “oxygen-rich”. NVOnH undergoes notable structural evolution and thermal instability during heating due to crystal water and O 2 release and decomposition. NVOnH and dehydrated NVOnH (NVO) deliver capacities of over 250 and 220 mAh g –1, respectively, despite their fast capacity decay in the first 20 cycles and low capacity retention after 100 cycles. Moreover, the reaction mechanism and reversibility of NVOnH and NVO during Na + -ion (de)insertion are investigated via in operando techniques. NVOnH experiences a two-phase and solid-solution reaction during discharge and charge processes, while NVO undergoes a different phase evolution (NVO starting with charging: two-phase reaction for the first charging and only solid solution for the following cycle; NVO starting with discharging: only a solid-solution reaction). In operando X-ray absorption spectroscopy demonstrates the variation of the oxidation state and the local structural environment of the V ion during Na + (de)insertion.
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Affiliations
Institute for Applied Materials (IAM), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, Eggenstein-Leopoldshafen, Karlsruhe D-76344, Germany
Helmholtz Institute Ulm for Electrochemical Energy Storage (HIU), Helmholtzstrasse 11, Ulm 89081, Germany
Deutsches Elektronen-Synchrotron (DESY), Notkestr. 85, Hamburg 22607, Germany
CELLS-ALBA Synchrotron, Cerdanyola del Valles, Barcelona E-08290, Spain
School of Chemical Engineering and Technology, Xi’an Jiaotong University, No. 28, West Xianning Road, Xi’an, Shaanxi 710049, China
Funding
Deutsche Forschungsgemeinschaft