單晶CoV2O6·2H2O納米帶的合成及其電化學(xué)性質(zhì)研究

周紅洋 朱永春 錢逸泰

(中國(guó)科學(xué)技術(shù)大學(xué)化學(xué)系，合肥微尺度物質(zhì)科學(xué)國(guó)家實(shí)驗(yàn)室，合肥 230026)

單晶CoV2O6·2H2O納米帶的合成及其電化學(xué)性質(zhì)研究

周紅洋 朱永春 錢逸泰＊

(中國(guó)科學(xué)技術(shù)大學(xué)化學(xué)系，合肥微尺度物質(zhì)科學(xué)國(guó)家實(shí)驗(yàn)室，合肥 230026)

本文描述了在反應(yīng)體系中不加入任何表面活性劑或模板的情況下，以水熱法合成正交相的CoV2O6·2H2O納米帶；燒結(jié)反應(yīng)得到其脫水鹽，即單斜相CoV2O6。通過(guò)X射線粉末衍射法(XRD)，場(chǎng)發(fā)射掃描電子顯微鏡(FE-SEM)，透射電子顯微鏡(TEM)和X射線光電子能譜(XPS)等研究了這些產(chǎn)物的物相、形貌和化學(xué)組成等，并通過(guò)熱重分析研究了CoV2O6·2H2O納米帶的熱穩(wěn)定性。此外，還觀察了CoV2O6·2H2O納米帶的形成過(guò)程，認(rèn)為其遵循一個(gè)經(jīng)典的固-液-固的形成機(jī)制。最后，通過(guò)鋰離子電池實(shí)驗(yàn)研究了CoV2O6·2H2O納米帶及其脫水鹽的電化學(xué)性質(zhì)，發(fā)現(xiàn)其放電容量分別達(dá)到980和675 mAh·g-1。

釩酸鹽；水熱法合成；電化學(xué)

0 Introduction

In the past decades,vanadium oxides and metal vanadates attracted much attention for their special physical,chemical properties,and potential applications in the fields such as catalysts[1],chemistry sensors[2], optical devices[3],and high-energy density lithium batteries[4].Recently,CoV2O6single crystals,grown in a closed crucible,was also found to display a large magnetic anisotropy and a 1/3 magnetization plateau underamagneticfieldappliedalongthec-axis[5].

Various efforts have been devoted to develop new approaches for the synthesis of 1D nanostructured materials.The synthesis of MnV2O6was carried out through the solid state reaction between Mn2O3andThe sintering reaction of hydrous compoundMnV2O6were precipitated from the solution of NaVO3and Mn(NO3)2[7].Stoichiometric and oxygen deficient CuV2O6was prepared via co-precipitation method[8]. The hydrothermal synthetic route was also applied in synthesizing metal vanadates 1D-nanostructured single-crystal.Rod-like anhydrous crystalline powders of MnV2O6were synthesized through the precipitating of mixed aqueous solution of Mn (CH3COO)2and V2O5[9]. Superlong β-AgVO3nanoribbons were synthesized from the hydrothermal reaction between V2O5and AgNO3in a solution containing a small amountofpyridine[10].BiVO4microspheres were selectively prepared through a hydrothermal process by using cetyltrimethylammonium bromide(CTAB) as a template-directing reagent[11].FeVO40.92H2O nanoneedles were fabricated via a hydrothermal method,and its electrochemical property was also investigated[12].

Previously,our group reported the synthesis of metal vanadates,i.e.,Chen et al.[13]fabricated CdV2O6nanowire arrays and tested its electrochemical property,Liuet al.[14],prepared single-crystal CaV6O16· 3H2O and VOx·nH2O nanoribbons via a hydrothermal reduction method and Liu et al.[15]synthesized AgVO3and MnV2O6,etc.Here we report the singlecrystalline CoV2O6·2H2O nanobelts preparation via a hydrothermal method without introduction into the reacting system of any templates or surfactants.The dehydrated salt was also prepared from the subsequent sintering treatment.Finally,theirelectrochemical properties were evaluated in lithium ion battery.

1 Experimental

All the reagents used in these experiments were of analytical purity, purchased from Shanghai Chemical Reagent Company,and were used without further purification.In a typical procedure,1 mmol CoCl2·6H2O and 2 mmol NH4VO3floccule-like white powders were put into the autoclave with 40 mL distilled water,all the solution was magnetically stirred for 15 min.Then,the autoclave was sealed, maintained at 180℃for 12 h,and air cooled to room temperature.The green sponge-like productwas transferred into a 100 mL beaker,filtrated,washed by distilled water and absolute ethanol at least three times.Finally,the product was dried in a vacuum at 60℃for 24 h and was collected for characterization. The corresponding dehydrated saltwasprepared through the subsequent treatment by sintering at 500℃ for 3 h in the atmosphere of argon.The product was also collected and characterized.

XRD (X-ray diffraction)patterns of the asprepared samples were recorded using a Philips XPert PRO SUPER X-raydiffractometerequipped with graphite monochromatized Cu Kα radiation (λ= 0.154 187 4 nm).The morphology and size of the final products were characterized by a series of microscopic techniques. Field scanning electron microscopy (FESEM)images were taken with JEOL-6700F scanning electronic microanalyzer. Transmission electron microscope (TEM)image and selected area electron diffraction (SAED)pattern were taken by Hitachi H-800 TEM with a tungsten filament and an accelerating voltage of200 kV.High resolution transmission electron microscope(HRTEM)image was recorded on a JEOL 2010 microscope.The samples used for TEM and HRTEM characterization were dispersed in absolute ethanol and were ultrasonicated before observation.The chemical composition of the nanobelts was obtained by X-ray photoelectron spectroscopy (XPS)on a VGESCALAB MKII X-ray photoelectronic spectrometer, using nonmonochromated Mg Kα radiation as the excitation. Thermogravimetric analysis(TGA)was carried out on a TGA-50 thermal analyzer(Shimadzu Corporation)at a heating rate of 10℃·min-1in flowing argon.

The electrode laminate for the electrochemical testing was prepared by casting a slurry consisting of CoV2O6·2H2O and its dehydrated salt powders(80wt%), acetylene black(10wt%),and poly(vinylidene fluoride) (PVDF;10wt%),dispersed in 1-methyl-2-pyrrolidinone (NMP)onto a copper foil.The laminates were then dried at 70℃for 1 h.The electrolyte was made with 1 mol· L-1LiPF6in ethylene carbonate (EC)and diethyl carbonate(DEC;1∶1 w/w).Cells were then tested on a multichannel battery cycler(Shenzhen Neware Co.Ltd.) and subjected to charge-discharge cycles at 0.30 mA· cm-2between 0.005 and 3.20 V(vs.Li metal).

2 Results and discussion

The XRD pattern of the as-products is shown in Fig.1,allthe peaks could be indexed as an orthorhombic phase,primitive lattice [space group: Pnma(No.62)]of CoV2O6·2H2O with the calculated lattice constants a=0.555 nm,b=1.062 nm,c=1.191 nm, which are in good agreement with the literature results (PDF No.80-0247).No other peaks of impurity are detected.XPS analysis is employed to further confirm the element component of CoV2O6·2H2O nanobelts.As shown in Fig.2(a),the survey spectra demonstrate the presence of Co,V,and O.The high-resolution XPS spectra from Co2p region in Fig.2(b)show the binding energies (BE)of Co2p1/2(797.079 eV)and Co2p3/2(780.774 eV),which are consistent with the literature values[16].

Fig.3(a)is the low magnification FESEM image of the as-prepared CoV2O6·2H2O single-crystal nanobelts. It shows that the product is consisted of a large quantity of nanobelts,with width of several hundreds nm,thickness of 10 nm and length up to several tens of micrometers.The twist and waving shapes of the nanoribbonsare apparent.Fig.3(b)isthe high magnification FESEM image of the product.It reveals some obvious features of belt-like structure.The morphologies and microstructures were further investigated through TEM technique.Fig.3(c)and(d) show the low magnification and high magnification TEM images of products,respectively.The TEM imagesindicate thatthe as-prepared productis uniform nanobelts in agreement with those of SEM results.As shown by the arrows in Fig.3(b)and(c),we could observe the nanoribbons have rectangle-like cross sections.The HRTEM image of the inset in Fig. 3(d)taken from a typical nanobelt displays the clearly resolved lattice fringes,indicating the integrality of crystallinity of the nanobelt.The inter-planar spacing is 0.366 7 nm,corresponding to the (121)plane of CoV2O6·2H2O orthorhombic phase.It substantiates that the nanobelts are single-crystalline ones.

Thermogravimetric analysis results further confirm the dehydrating process.As shown in Fig.4,the weight becomes constant up to 500℃,indicating that the dehydrating reaction happens from room temperature to 500℃.And the overall percentage weight loss in the thermogravimetric analysis is 11.89%,very close to the calculated value(12.30%).The corresponding sintering experiment is done as follows:the as-prepared CoV2O6· 2H2O nanobelts were heated from room temperature to 500℃at a heating rate of 10℃·min-1in flowing argon. After sintering for 3 h,the product was naturally cooled to room temperature,collected for characterization.As in Fig.5 (a),the XRD pattern could be indexed as a monoclinic phase,end-centered lattice[space group:C2 (No.5)]of CoV2O6with the calculated lattice constants, a=0.924 5 nm,b=0.349 8 nm,c=0.662 2 nm,β=111.05°, which are accordant with the literature results(PDF No. 77-1174).More details of CoV2O6are shown in Fig.5(b) and (c).The SEM image in Fig.5(b)shows that the CoV2O6nanocrystals comprising this pre-dehydrated product are 1D nanostructure with clear broken facets and relatively-short aspect ratio,which is possibly ascribed to the sintering treatment.The typical TEM image of a single CoV2O6nanorod is also recorded,and the corresponding HRTEM image(inset)displays these clearly resolved lattice fringes with inter-planar spacings of 0.306 8 nm and 0.183 73 nm,which are corresponding tothe(111)and(403)planes of the CoV2O6monoclinic phase.No vacancy nor dislocation is detected among these TEM images,indicating that CoV2O6nanorods are all well-crystallized under the sintering condition.

In order to investigate the growing process of the single-crystalline CoV2O6·2H2O nanobelts,a series of time-dependent experiments were carried out,and the products of different stages at the temperature of 180℃:(a)15 min.(b)30 min.(c)2.0 h.(d)4.0 h.,were collected and characterized.The XRD patterns shown in Fig.6 indicate that all the products could be indexed as an orthorhombic phase of CoV2O6·2H2O and no other peaks are detected.The XRD result also implies that the phase of CoV2O6·2H2O forms soon at the initial stage of the reacting process [as shown in Fig.6(a)and(b),the phase forms after 30 min].The SEM images were also employed to observe the overall growing process.A mixture of floccules and microcrystals is formed at the initial stage (15～30 min).As shown in Fig.7 (a)and (b),these floccules include microplates with width of several micrometers and thickness of tens nanometers,the microcrystals are regular polyhedron in morphologies and tens of micrometers in size (inset).Subsequently,with the extension of reaction time,the yield of microcrystals decreases sharply.With the yield offloccules increasing, the main content of floccules is transformed into the belt-like microstructure[shown in Fig.7(c)].When the reaction time is extended to 4.0 h, the product is almost transformed into CoV2O6·2H2O nanobelts without any nanocrystals of other morphology.Afterwards,the apparent morphology of the product will not change obviously by extending the reacting time.Although the exact mechanism is still unclear,we believe that the growth of nanobelts is controlled by a solid-solution-solid process(SSS), and the forming process of CoV2O6·2H2O singlecrystal nanobelts might be described by the reaction:

View Within Article Previously,Baudrin et al[16]prepared a series of cobalt-based vanadates through the coprecipitation method,and investigated their electrochemical properties vs.lithium.Herein,the single-crystalline CoV2O6·2H2O nanobelts and their dehydrated salt wereelectrochemicallytreated in lithium ion battery to evaluate their electrochemical property.Fig.8 shows the first discharge curves of CoV2O6·2H2O nanobelts and its dehydrated salt at a current density of 0.3 mA·cm-2.The discharge capacity of CoV2O6·2H2O nanobelts could reach 980 mAh·g-1and its dehydrated salt can reach 675 mAh· g-1.The rates of dischargeability of CoV2O6·2H2O nanobelts and its dehydrated salt are shown in Fig.9.After being cycled for 10 times,the capacity retention of CoV2O6·2H2O nanobelts is 44% (about 430 mAh· g-1),and CoV2O6is only 10% (about 70 mAh·g-1).Investigation for the attenuation is still undergoing.

3 Conclusions

In summary,the single-crystalline CoV2O6·2H2O nanobeltswere prepared and characterized.The forming process was observed and discussed.The single-crystalline CoV2O6·2H2O nanobelts and its dehydrated salts electro-chemically treated in lithium ion battery were employed to evaluate their electrochemical property,and the result suggests their potential applications in high-energy battery field.

Acknowledgment:The work was supported by the 973 Project of China(No.2011CB935901),the National Nature Science Fund of China（No.91022033）.

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Synthesis and Electrochemical Properties of Single-Crystalline CoV2O6·2H2O

ZHOU Hong-Yang ZHU Yong-Chun QIAN Yi-Tai＊
(Department of Chemistry and Hefei National Laboratory for Physical Sciences at Microscale, University of Science and Technology of China,Hefei 230026,China)

Single-crystalline orthorhombic CoV2O6·2H2O nanobeltswaslarge-scale prepared through a hydrothermal method without any templates or surfactants.The corresponding dehydrated salt of monoclinic CoV2O6was prepared by the subsequent sintering treatment.The products were all collected and characterized by XRD,FESEM,TEM,SAED,HRTEM,XPS and Thermogravimetric analytical techniques.Thermogravimetric analysis indicates its thermal stability.The forming process was discussed,and we believe that the growth of nanobelts follows the typical solid-solution-solid process.Finally,the single-crystalline CoV2O6·2H2O nanobelts and its dehydrated salt demonstrat the first discharge of 980 mAh·g-1and 675 mAh·g-1,respectively,upon electrochemical treatment in lithium ion battery.

vanadate;hydrothermal synthesis;electrochemistry

O614.81+2；O614.51+1

A

1001-4861(2011)07-1393-06

2010-12-10。收修改稿日期：2011-03-15。

國(guó)家973計(jì)劃(No.2011CB935901)和國(guó)家自然科學(xué)基金(No.91022033)資助項(xiàng)目。

＊通訊聯(lián)系人。E-mail：ytqian@ustc.edu.cn