Burova Daria, Shakhova Iaroslava, Morozova Polina, Iarchuk Anna, Drozhzhin Oleg A, Rozova Marina G, Praneetha S, Murugan Vadivel, Tarascon Jean-Marie, Abakumov Artem M
Center for Energy Science and Technology, Skolkovo Institute of Science and Technology Nobel Str. 3 143026 Moscow Russia
Chemical Department, Moscow State University Leninskie Gory, 1 119234 Moscow Russia.
RSC Adv. 2019 Jun 20;9(34):19429-19440. doi: 10.1039/c9ra02257k. eCollection 2019 Jun 19.
NASICON-structured NaVO (PO)F (0 < ≤ 1) solid solutions have been prepared using a microwave-assisted hydrothermal (MW-HT) technique. Well-crystallized phases were obtained for = 1 and 0.4 by reacting VO, NHHPO, and NaF precursors at temperatures as low as 180-200 °C for less than 15 min. Various available and inexpensive reducing agents were used to control the vanadium oxidation state and final product morphology. The vanadium oxidation state and O/F ratios were assessed using electron energy loss spectroscopy and infrared spectroscopy. According to electron diffraction and powder X-ray diffraction, the NaVO (PO)F solid solutions crystallized in a metastable disordered 4/ structure ( = 6.38643(4) Å, = 10.62375(8) Å for NaVO(PO)F and = 6.39455(5) Å, = 10.6988(2) Å for NaVO(PO)F). With respect to electrochemical Na (de)insertion as positive electrodes (cathodes) for Na-ion batteries, the as-synthesized materials displayed two sloping plateaus upon charge and discharge, centered near 3.5-3.6 V and 4.0-4.1 V Na/Na, respectively, with a reversible capacity of ∼110 mA h g. The application of a conducting carbon coating through the surface polymerization of dopamine with subsequent annealing at 500 °C improved both the rate capability (∼55 mA h g at a discharge rate of 10C) and capacity retention (∼93% after 50 cycles at a discharge rate of C/2).
采用微波辅助水热(MW-HT)技术制备了NASICON结构的NaVO(PO)F(0<x≤1)固溶体。通过在低至180 - 200℃的温度下反应VO、NHHPO和NaF前驱体不到15分钟,得到了x = 1和0.4时结晶良好的相。使用各种可用且廉价的还原剂来控制钒的氧化态和最终产物的形态。利用电子能量损失谱和红外光谱评估钒的氧化态和O/F比。根据电子衍射和粉末X射线衍射,NaVO(PO)F固溶体结晶为亚稳无序的4/结构(对于NaVO(PO)F,a = 6.38643(4) Å,c = 10.62375(8) Å;对于NaVO(PO)F,a = 6.39455(5) Å,c = 10.6988(2) Å)。关于作为钠离子电池正极(阴极)的电化学Na(脱)嵌入,合成的材料在充电和放电时显示出两个倾斜的平台,分别以接近3.5 - 3.6 V和4.0 - 4.1 V Na/Na为中心,可逆容量约为110 mA h g。通过多巴胺的表面聚合随后在500℃退火施加导电碳涂层,提高了倍率性能(在10C放电速率下约为55 mA h g)和容量保持率(在C/2放电速率下50次循环后约为93%)。