Superior Na-storage performance of molten-state-blending-synthesized monoclinic NaVPO4F nanoplates for Na-ion batteries

A superior monoclinic NaVPO4F nanoplate for Na-ion batteries has been prepared by a molten-state-blending technique. By this molecular level blending method, a nanoscale-laminated NaVPO4F@C sample with high crystallinity can be obtained. High thermal stability, stable Na+ insertion/extraction and su...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (47), p.24201-24209
Hauptverfasser: Ling, Moxiang, Li, Fan, Yi, Hongming, Li, Xianfeng, Hou, Guangjin, Zheng, Qiong, Zhang, Huamin
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container_issue 47
container_start_page 24201
container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 6
creator Ling, Moxiang
Li, Fan
Yi, Hongming
Li, Xianfeng
Hou, Guangjin
Zheng, Qiong
Zhang, Huamin
description A superior monoclinic NaVPO4F nanoplate for Na-ion batteries has been prepared by a molten-state-blending technique. By this molecular level blending method, a nanoscale-laminated NaVPO4F@C sample with high crystallinity can be obtained. High thermal stability, stable Na+ insertion/extraction and superior electron/Na+ transport of NaVPO4F have been elucidated by temperature-dependent IR, in situ XRD and kinetic investigations. Accordingly, the as-prepared NaVPO4F with moderate carbon coating exhibits superior Na-storage performance. It can deliver a high initial specific capacity of 135.0 mA h g−1 at 0.2C, ultra-high rate performance (up to 112.1 mA h g−1 at 30C) and super-stable cycling performance (capacity fading rate of 0.0064% per cycle during 1500 cycles at 20C). The potential application of NaVPO4F as the anode has been explored, and a symmetrical battery with NaVPO4F as both the anode and cathode has been successfully assembled for the first time. More significantly, in situ XRD and ex situ NMR have been employed to explore the charge–discharge behavior in a Na-ion battery, and the result clearly demonstrates that less than one Na has been intercalated/extracted from NaVPO4F during the charging/discharging process.
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By this molecular level blending method, a nanoscale-laminated NaVPO4F@C sample with high crystallinity can be obtained. High thermal stability, stable Na+ insertion/extraction and superior electron/Na+ transport of NaVPO4F have been elucidated by temperature-dependent IR, in situ XRD and kinetic investigations. Accordingly, the as-prepared NaVPO4F with moderate carbon coating exhibits superior Na-storage performance. It can deliver a high initial specific capacity of 135.0 mA h g−1 at 0.2C, ultra-high rate performance (up to 112.1 mA h g−1 at 30C) and super-stable cycling performance (capacity fading rate of 0.0064% per cycle during 1500 cycles at 20C). The potential application of NaVPO4F as the anode has been explored, and a symmetrical battery with NaVPO4F as both the anode and cathode has been successfully assembled for the first time. 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The potential application of NaVPO4F as the anode has been explored, and a symmetrical battery with NaVPO4F as both the anode and cathode has been successfully assembled for the first time. 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More significantly, in situ XRD and ex situ NMR have been employed to explore the charge–discharge behavior in a Na-ion battery, and the result clearly demonstrates that less than one Na has been intercalated/extracted from NaVPO4F during the charging/discharging process.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c8ta08842j</doi><tpages>9</tpages></addata></record>
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source Royal Society Of Chemistry Journals 2008-
subjects Anodes
Blending
Chemical synthesis
Discharge
NMR
Nuclear magnetic resonance
Rechargeable batteries
Sodium-ion batteries
Specific capacity
Storage
Storage batteries
Temperature dependence
Thermal stability
title Superior Na-storage performance of molten-state-blending-synthesized monoclinic NaVPO4F nanoplates for Na-ion batteries
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