Single crystalline Nb2O5 nanorods have been successfully synthesized by a soft chemical process, in which only metal Nb powder and water were used as the starting materials. The synthesized Nb2O5 nanorods are highly crystalline and their growth is along [001] direction. The diameter of the nanorods is found to be ca. 50 nm and their lengths up to several micrometers. Based on the experimental results of XRD, SEM, and TEM measurements, the possible mechanism for the formation of Nb2O5 nanorods was discussed.
1. Introduction
Since the discovery of carbon nanotubes in 1991 [1], one-dimensional (1D) nanomaterials including nanorods, nanotubes, nanowires, nanofibers, nanobelts, and nanoribbons have attracted much attention due to their physical and chemical properties different from those of bulk materials [2]. In the past decades, a large number of 1D oxide nanomaterial have been synthesized, such as TiO2 [3], MnO2 [4], ZnO [5], SnO2 [6], VOx [7], MoO3 [8], Ga2O3 [9], Ta2O5 [10], In2O3 [11], and Nb2O5 [12]. Among them, Nb2O5 is an important semiconductor oxide with a wide band gap [13] and had been widely used in electrochromic devices [14], catalysts [15], chemical sensors [16], optical filters [17], solar cells [18], and lithium batteries [19]. As is well known, Nb2O5 has many polymorphic forms based on the octahedrally coordinated niobium atoms [20]. These polymorphs are identified with a variety of prefixes [21] such as B-Nb2O5 (PdF3 rutile structure), H-Nb2O5 (ReO3-type block, 3×3 or 3×5 octahedra), and N-Nb2O5 (ReO3-type block, 4×4 octahedral). Among the niobium oxides, Nb2O5 is the most stable and exhibits the excellent chemical stability and corrosion resistance in both acid and base media [22]. So far, niobium oxide fibers have been prepared by using an electrospinning method [23]. Mozetič et al. [24] has synthesized Nb2O5 nanowires via a cold plasma treatment in the presence of a high neutral oxygen flux. Niobia-phase nanorods [25] were obtained by the hydrothermal treatment of a niobium peroxo complex precursor at 140°C. Hu et al. [26] reported the synthesis of Nb2O5 nanocables using NbCl5 as a precursor. Kobayashi et al. [27] prepared Nb2O5 nanotubes using the layered K4Nb6O17 as a precursor, in which K4Nb6O17 was formed at over 1050°C. Nb2O5 nanotubes have also been obtained using HF solution as a reactant [28]. Using amorphous Nb2O5·nH2O as a precursor, Nb2O5 nanorods [29] were formed at a high temperature. More recently, Nb2O5 nanobelts were synthesized by using a hydrothermal route [30]. To the best of our knowledge, however, the synthesis of niobium oxide with 1D nanostructure has not been reported by using a soft chemical process. Here, we first fabricated Nb2O5 nanorods starting from metal Nb powder by a soft chemical process, without templates or catalysts, and using only the raw material and water. Furthermore, the possible mechanism for the formation of nanorods was discussed according to the experimental results.
2. Experimental
A soft chemical process was developed to prepare Nb2O5 nanorods. In a typical procedure, 0.1 g of the commercial metal Nb powder was dispersed into 40 mL distilled water and stirred, then transferred into a 50 mL Teflon-lined autoclave, and kept in an oven at 200°C for 3 to 30 days. The final products were washed with distilled water and then dried in the air.
Scanning electron (SEM) and transmission electron microscopy (TEM) were taken on a Philip-XL30 instrument and a JEOL 2010 instrument, respectively. X-ray diffraction (XRD) pattern was recorded on a PANalytical X’Pert spectrometer using the Co Kα radiation (λ=1.78897 Å) and the data would be changed to Cu Kα data.
3. Results and Discussion
Figure 1 shows the SEM images of the raw Nb powder and the products obtained at 200°C for different reaction times. It clearly shows that the SEM morphology of the products is entirely different from the raw material Nb metal powder. Only particles with different sizes were detected in the raw material, as shown in Figure 1(a). After the raw Nb metal powder was treated in H2O at 200°C for 3 days, a large number of sheet-like and nanorod-like products were observed, as depicted in Figure 1(b). With increasing reaction time, numerous nanorods with a bundle-like structure were formed and the sheet-like products disappeared, as depicted in Figures 1(c)–1(f). It can also be found that the length of these nanorods increased significantly with reaction time. These nanorods lie close to each other and their lengths up to several micrometers.
SEM images of (a) raw material Nb and the products synthesized at 200°C for different reaction times (b) 3, ((c), (d)) 15, and ((e), (f)) 30 days.
The morphologies of the product can be further confirmed by TEM measurements. Figure 2(a) clearly shows a single nanorod obtained at 200°C for 30 days. The diameter of the nanorod is found to be ca. 50 nm. Figure 2(b) is a high-resolution TEM image and clearly reveals that the formed nanorods are single crystalline. The lattice fringes correspond to a d-pacing of 0.393 and 0.315 nm, respectively. The typical selected area electron diffraction (SAED) taken from a single nanorod is shown in Figure 2b (inset). The pattern exhibits broadened and strong spots along the growth direction of the nanorods which can be attributed to the essentially asymmetric 1D nature of the long and thin nanorods. These results also indicate that the growth of nanorods is along [001] direction.
The TEM images of the product synthesized at 200°C for 30 days: (a) low magnification, and (b) high magnification (inset, SAED).
XRD measurement was used to identify the crystalline structure of the product, as shown in Figure 3. Besides raw Nb metal, the main phase detected was Nb2O5 which could be indexed to Nb2O5 (JPCDS 27-1313) with an orthorhombic structure. This result is in agreement with the TEM observations. Based on the experimental results of XRD, SEM, and TEM measurements, a possible model for the formation of Nb2O5 nanorods is suggested as follows: (i) the surface of the metal Nb powder was oxidized by oxygen in water under the hydrothermal conditions, and the sheet-like products were formed; (ii) the sheet-like products were splitted in order to release strong stress and lower the total energy, and then the nanorods were formed. Therefore, the formation of bundle-like structure can be contributed to the fact that the splitting of the sheets-like products is complete.
The XRD pattern of the product synthesized at 200°C for 30 days (●: Orthorhombic Nb2O5,: ▾: Cubic Nb).
In the present work, metal Nb powder was used as a starting material and reacted with water under the hydrothermal conditions to yield single crystalline Nb2O5 nanorods. Although the purity of Nb2O5 nanorods in the final product is still to be improved, the synthetic route is very simple, in which templates or catalysts were not introduced into the reaction system. Comparing with the normal hydrothermal process, such a synthetic route took a long reaction time. This might be related to that the hydrothermal reaction was accelerated in the presence of templates or catalysts.
4. Conclusions
In summary, single crystalline Nb2O5 nanorods were successfully synthesized by a soft chemical process, in which the metal Nb powder and water were used as the precursors. The synthesized nanorods are highly crystalline and their growth direction is along [001]. The diameter of the nanorods is found to be ca. 50 nm and their lengths up to several micrometers. Furthermore, the work is underway to optimize the process and increase purity of nanorods in the product. Compared with other synthetic routes, no any catalysts or templates were introduced into the reaction system. We believe that the synthetic route of Nb2O5 nanorods from the metal Nb powder has the potential to prepare 1D nanostructural metal oxides.
Acknowledgments
This work was financially supported by the National High Technology Research and Development Program (“863’’) and Ministry of Education under Grant nos. 2007AA05Z438 and 200803860004, Science and Technology Program from Fujian Province (nos. 2008J0332, 2007HZ0005-1), and the startup funds from the Ministry of Education and Fuzhou University.
IijimaS.Helical microtubules of graphitic carbon1991354634856582-s2.0-0342819025CuiY.WeiQ.ParkH.LieberC. M.Nanowire nanosensors for highly sensitive and selective detection of biological and chemical species200129355331289129210.1126/science.10627112-s2.0-0035902938KasugaT.HiramatsuM.HosonA.SekinoT.NiiharaK.Titania nanotubes prepared by chemical processing19991115130713112-s2.0-0033363865WangX.LiY.Selected-control hydrothermal synthesis of α- and β-MnO2 single crystal nanowires200212412288028812-s2.0-003583129010.1021/ja0177105ParkW. I.KimJ. S.YiG.-C.LeeH.-J.ZnO nanorod logic circuits200517111393139710.1002/adma.2004017322-s2.0-20444449735HuangH.TanO. K.LeeY. C.TseM. S.GuoJ.WhiteT.In situ growth of SnO2 nanorods by plasma treatment of SnO2 thin films200617153668367210.1088/0957-4484/17/15/0082-s2.0-33748904802WeiM.SugiharaH.HonmaI.IchiharaM.ZhouH.A new metastable phase of crystallized V2O4⋅0.25H2O nanowires: synthesis and electrochemical measurements200517242964296910.1002/adma.2005016082-s2.0-29744464676LuoH.WeiM.WeiK.A new metastable phase of crystallized MoO3⋅0.3H2O nanobelts20091131859010.1016/j.matchemphys.2008.07.0592-s2.0-56449093040ZhangJ.JiangF.YangY.LiJ.Catalyst-assisted vapor-liquid-solid growth of single-crystal Ga2O3 nanobelts20051092713143131472-s2.0-003592704610.1021/jp0511247El-SayedH. A.BirssV. I.Controlled interconversion of nanoarray of Ta dimples and high aspect ratio Ta oxide nanotubes2009941350135510.1021/nl803010v2-s2.0-65249083864ChiquitoA. J.LanfrediA. J. C.de OliveiraR. F.M.PozziL. P.LeiteE. R.Electron dephasing and weak localization in Sn doped In2O3 nanowires200775143914432-s2.0-003332184910.1021/nl070178kSayamaK.SugiharaH.ArakawaH.Photoelectrochemical properties of a porous Nb2O5 electrode sensitized by a ruthenium dye19981012382538322-s2.0-0000999346HaraK.HoriguchiT.KinoshitaT.SayamaK.SugiharaH.ArakawaH.Highly efficient photon-to-electron conversion with mercurochrome-sensitized nanoporous oxide semiconductor solar cells20006421151342-s2.0-0034734470VargheseB.HaurS. C.LimC.-T.Nb2O5 nanowires as efficient electron field emitters200811227100081001210.1021/jp800611m2-s2.0-49249116466TanabeK.Catalytic application of niobium compounds2003781–4657710.1016/S0920-5861(02)00343-72-s2.0-0037469456Gimon-KinselM. E.BalkusK. J.Jr.Pulsed laser deposition of mesoporous niobium oxide thin films and application as chemical sensors19992811131232-s2.0-0032664324SieberI.HildebrandH.FriedrichA.SchmukiP.Formation of self-organized niobium porous oxide on niobium2005719710010.1016/j.elecom.2004.11.0122-s2.0-10644282898JoseR.ThavasiV.RamakrishnaS.Metal oxides for dye-sensitized solar cells200992228930110.1111/j.1551-2916.2008.02870.x2-s2.0-60849123909WeiM.WeiK.IchiharaM.ZhouH.Nb2O5 nanobelts: a lithium intercalation host with large capacity and high rate capability200810798098310.1016/j.elecom.2008.04.0312-s2.0-45649084632WellsA. F.19845thOxford, UKOxford ScienceGatehouseB. M.WadsleyA. D.The crystal structure of the high temperature form of niobium pentoxide196417121545155410.1107/S0365110X6400384XVenkatarajS.DreseR.LieschCh.KappertzO.JayavelR.WuttigM.Temperature stability of sputtered niobium-oxide films20029184863487110.1063/1.14580522-s2.0-0037091509ViswanathamurthiP.BhattaraiN.KimH. Y.LeeD. R.KimS. R.MorrisM. A.Preparation and morphology of niobium oxide fibres by electrospinning20033741-2798410.1016/S0009-2614(03)00702-42-s2.0-0038182744MozetičM.CvelbarU.SunkaraM. K.VaddirajuS.A method for the rapid synthesis of large quantities of metal oxide nanowires at low temperatures200517172138214210.1002/adma.2005007282-s2.0-24644507954LeiteE. R.VilaC.BettiniJ.LongoE.Synthesis of niobia nanocrystals with controlled morphology200611037180881809010.1021/jp06425442-s2.0-33749610826HuW.ZhaoY.LiuZ.ZhuY.NbS2/Nb2O5 nanocables20071891510.1088/0957-4484/18/9/0956052-s2.0-33947498468KobayashiY.HataH.SalamaM.MalloukT. E.Scrolled sheet precursor route to niobium and tantalum oxide nanotubes2007772142214510.1021/nl07082602-s2.0-34547572728YanC.XueD.Formation of Nb2O5 nanotube arrays through phase transformation20082051055105810.1002/adma.2007017522-s2.0-47249096428ZhouY.QiuZ.LüM.ZhangA.MaQ.Preparation and spectroscopic properties of Nb2O5 nanorods2008128813691372WeiM.QiZ.-m.IchiharaM.ZhouH.Synthesis of single-crystal niobium pentoxide nanobelts200856112488249410.1016/j.actamat.2008.01.0492-s2.0-44449170263