- Nano Express
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In situ Precursor-Template Route to Semi-Ordered NaNbO3 Nanobelt Arrays
Nanoscale Res Lettvolume 6, Article number: 14 (2010)
We exploited a precursor-template route to chemically synthesize NaNbO3 nanobelt arrays. Na7(H3O)Nb6O19·14H2O nanobelt precursor was firstly prepared via a hydrothermal synthetic route using Nb foil. The aspect ratio of the precursor is controllable facilely depending on the concentration of NaOH aqueous solution. The precursor was calcined in air to yield single-crystalline monoclinic NaNbO3 nanobelt arrays. The proposed scheme for NaNbO3 nanobelt formation starting from Nb metal may be extended to the chemical fabrication of more niobate arrays.
One-dimensional (1D) nanostructures are receiving an ever-increasing amount of attention from researchers in various disciplines because of their unusual quantum properties to their bulk counterparts and potential use as building blocks for the next generation of nanoscale optical, electronic, photonic, and biological devices [1, 2]. Ordered functional arrays or chemically defined surfaces with fascinating quantum behaviour are more attractive nanostructures owing to their applications in high-density memories, sensors, lasers, and photonic crystals. Although numerous efforts have been invested in developing simple and low-cost fabrication techniques for the growth of high-quality 1D materials in a relatively large scale [3–10], the ability to fabricate ordered 1D micro- and nanostructures in a desired pattern with controllable size and shape uniformity is a key challenge in enabling their improved technological applications and has opened up the minds of new generation of materials scientists about the potential of nanoscience and technology [11, 12].
Alkaline niobates is one class of widely investigated ternary materials because of their optical, ferroelectric, and piezoelectric properties [13–19]. To date, many niobium-containing perovskite materials have been synthesized through various kinds of methods and exhibit wide applications in nonlinear optics, pyroelectric detectors, and optical memories, etc. NaNbO3 belongs to a technologically important group of perovskite materials, which comprises a three-dimensional framework of corner-sharing NbO6 octahedra with Na cations occupying their cavities [20–22]. Tilting of NbO6 octahedra at different temperature brings different phases (orthorhombic, monoclinic, and cubic phase). Generally, the shape of crystalline particles depends on their internal structures . This means that materials with a cubic or pseudocubic structure will normally form isotropic particles in a thermodynamic decided process. Actually, till now there are few reports about high aspect ratio 1D NaNbO3 micro/nano structures, which provide a good system to study the size and dimensionality dependences of the physical properties. Herein, we exploit a facile precursor-template route to chemically fabricate NaNbO3 nanobelts. After a solid-phase transformation of Na7(H3O)Nb6O19·14H2O precursors in air, semi-ordered NaNbO3 nanobelt arrays were yielded without morphology deformation. In this proposed scheme, the aspect ratio and uniformity of the precursor and NaNbO3 nanobelts are controllable. Low concentration of NaOH in this process also avoids strong corrosive effect.
A typical synthesis was performed as follows. A piece of Nb foil (6 × 6 × 0.5 mm) was pretreated by sonication in ethanol for 10 min and laid flat in a Teflon-lined stainless steel autoclave (capacity, 30 mL). Twenty millilitres 1.0 M NaOH solution mixed with 3 mL H2O2 (PH = 13.2) was then filled into the autoclave that was sealed and put into an electric oven. The concentration of NaOH was changed from 0.5 to 1.5 M to tune the aspect ratio of precursor nanobelts. The temperature of the electric oven was set at 150–220°C and kept the reaction lasted for 10–24 h under autogenous pressure. After the autoclave was air-cooled to room temperature, Nb foil was dissolved completely, and the white sheet-like powders were collected, rinsed with deionized water, and dried at 40–60°C for 2–5 h in air. NaNbO3 nanobelt arrays could be obtained by calcining the precursor at 500–550°C for 1–4 h.
The as-prepared samples were characterized by an X-ray diffractometer (XRD) on a Rigaku-DMax 2400 diffractometer equipped with the graphite monochromatized Cu Kα radiation flux at a scanning rate of 0.02°/s in the 2θ range 5–80°. Scanning electron microscopy (SEM) images were taken with a JEOL-5600LV scanning electron microscopy, using an accelerating voltage of 20 kV. Energy-dispersive X-ray (EDX) microanalysis of the samples was performed during SEM measurements. The structures were investigated by transmission electron microscopy (TEM, Philips, Tecnai G220, operated at 200 kV). Thermogravimetric analysis and differential scanning calorimetry (TG/DSC, SDT Q600, TA) were employed to analyse the thermal behaviours of the synthesized precursor in N2 atmosphere at a heating rate of 10°C/min. UV–visible (UV–Vis) spectra of the samples were measured on a UV–Vis-NIR spectrophotometer (JASCO-V570). The photoluminescence (PL) spectra were measured at room temperature in the range of 310–700 nm using a Xe lamp with a wavelength of 290 nm as the excitation source. The infrared (IR) spectrum was measured by KBr pellet method (using a Nicolet NEXUS infrared spectroscopy) in the range of 400–4,000 cm-1.
Results and Discussion
Hydrothermal technique has been most popular and widely used in the synthesis of advanced materials of different disciplines owing to its advantages in terms of high reactivity of reactants, formation of metastable and low energy consumption. In our scheme, Na7(H3O)Nb6O19·14H2O nanobelts were firstly synthesized under mild hydrothermal conditions. XRD pattern of the obtained product is shown in Figure 1a. The major diffraction peaks can be indexed as the Na7(H3O)Nb6O19·14H2O with an orthorhombic lattice (JCPDS card no. 84-0188). The broad diffractive peaks are attributed to the nanosize of the sample. Moreover, a characteristic diffraction peak from remnant Nb foil is detected. The molecular structure of Na7(H3O)Nb6O19·14H2O is further supported by the solid-state IR spectrum (Figure 1b), which is in agreement with the literature values .
It has been reported that as the concentration of AOH (A = Na, K) increases in solution, the Lindquist compound is salted out as a major product . In each Lindquist ion of Na7(H3O)Nb6O19·14H2O, six NbO6 octahedra compose a bigger octahedron by sharing edges, Na atoms are scattered within the vacancies between the Lindquist octahedral sites. Further examination of the crystal structure of Na7(H3O)Nb6O19·14H2O reveals that the preferential orientation of the Na7(H3O)Nb6O19·14H2O is along c-axis. Considering that no templates and surfactants are used, it is the internal crystal structure that induces 1D growth of the Lindquist composite. Because of the coexistence of H2O2 and NaOH, alkaline oxidant solution is formed in the autoclave. The metal substrate is oxidated continuously by H2O2 into Nb2O5 which is subsequently dissolved by NaOH. Metastable phases often crystallize first at low temperature because their nucleolus may require lower free energy and lower supersaturation to form in the nucleation-controlled regime. Therefore, Na7(H3O)Nb6O19·14H2O is crystallized and precipitated out of the solution.
The low-magnification SEM images of Na7(H3O)Nb6O19·14H2O (Figure 2a, b) have been taken from randomly selected areas, and as such, these are representative of the overall sizes and shapes in the samples. It is seen that ultralong Na7(H3O)Nb6O19·14H2O nanobelt arrays are with honeycomb-like micropatterns. The length is in micrometer range. Furthermore, the high-magnification SEM images in Figure 2c, d reveal that these nanobelts are formed uniformly and compactly with typical widths of ~300 nm and thicknesses of ~80 nm. TEM and HRTEM images provide further insight into the microstructural details of belt-like nanostructures. Figure 2e shows that the nanobelt has a uniform width, and there are some contrasty stripes along the growth direction. A magnified image of a single nanobelt in Figure 2f exhibits clearly that the 1D structure is the belt-like aggregate morphology. The nanobelt bundles are essentially aligned in the same orientation and have different packing density resulting in the contrasty stripes in TEM observation. A cross-section of Na7(H3O)Nb6O19·14H2O nanobelt array is shown in Figure 3a. It is found that the nanobelts are typically ~50 μm in length, and they grow on an irregular-shaped microcrystal layer. EDX spectrum of the substrate in Figure 3b indicates the presence of Na, Nb, and O. Therefore, since the Nb metal foil is dissolved completely, it is a kind of sodium niobate substrate that induces the growth of Na7(H3O)Nb6O19·14H2O nanobelt.
We can control the aspect ratio and micropatterns of Na7(H3O)Nb6O19·14H2O structures by tuning NaOH concentration in the wet chemistry process. At a concentration of 0.5–0.8 M, hedgehog-like patterns are formed. The dense Na7(H3O)Nb6O19·14H2O microbars are with widths mostly less than 1 μm and thicknesses around 150 nm (Figure 4a, b). However, when the concentration is increased to 1–1.5 M, the nanobelts become so long that they gather compactly and overspread the substrate (Figure 4c, d). Therefore, we conclude that the alkaline concentration has a significant influence on morphology.
The thermal decomposition process of Na7(H3O)Nb6O19·14H2O is shown in Figure 5a. As seen in TG curve, there is only one evident step involving dehydration. The weight of the sample significantly decreases in the temperature range of 80~290°C. Furthermore, between 290 and 515°C, the mass loss becomes quite slow and ceases at higher temperature (around 515°C). The total mass loss is about 9%, slightly smaller compared with standard value (11.3%). It is possible that some impurities, such as the microparticles below the nanobelt arrays, bring the difference. DSC plot for the decomposition recorded in nitrogen gas shows two peaks: one is endothermic event corresponding to the rapid release of H2O, and the other is exothermic peak at around 490°C corresponding to the transformation into NaNbO3 phase, which can be completed at around 515°C. Thermal decomposition of the precursor nanobelts under normal atmospheric conditions gives rise to the formation of a pure monoclinic NaNbO3 phase. As indicated in the Figure 5b, all the peaks in XRD pattern can be indexed well as the pure phase (JCPDS card no. 74-2441). During the thermal conversion process, NbO6 octahedra change from edge-sharing to corner-sharing. This structural difference has an important effect on the gap between the valence band and conductive band of niobates, which can be reflected in the optical absorption spectra of the as-prepared samples. UV–Vis spectra of the precursor, final product, and bulk NaNbO3 are shown in Figure 5c. The precursor has an absorption peak at around 250 nm (a) due to the Lindquist units including six edge-sharing NbO6 octahedra. However, the peak shifts to above 300 nm in final NaNbO3 product (b) that comprises corner-sharing NbO6 octahedra. The change may originate from the difference in Nb–O bond distances in configuration of NbO6 octahedra, which also further confirms that corner-sharing NbO6 octahedra are more stable than edge-sharing ones. When compared with UV absorption peak of bulk NaNbO3 (c) at around 362 nm, the optical absorption edge of NaNbO3 nanobelts shifts towards the lower wavelength, indicating an increase in band gap. Due to the quantum size effect in nanosized semiconductors, the band gap increases when the size of belt-like nanomaterials is decreased, resulting in a blueshift of absorption bands. PL spectra of NaNbO3 nanobelts were also been measured, as shown in Figure 5d. The spectra consist of a UV emission peak and two violet emission peaks in visible region. It is found that the UV peak position is at approximately 368 nm which can be attributed to free exciton emission. Two strong visible peaks dominate the PL spectra, which locate at λ = 421 and 433 nm. The spectra suggest that niobate framework is directly involved in the photoluminescence effect. The heat treatment increases the stability of Nb–O–Nb bonds and introduces different kinds of defect centres acting as traps for charge carriers, therefore increasing the probability for electrons to reach an electron trap, such as oxygen vacancy, and leading to the luminescence effect. The optical properties of NaNbO3 thus open up opportunities for exploiting advanced NaNbO3-based optical nanodevices.
Evidence that the nanobelts have retained their morphology is shown in Figure 6. The NaNbO3 nanobelt arrays still have ordered honeycomb-like micropatterns (Figure 6a). A high-magnification SEM image (Figure 6b) indicates NaNbO3 nanobelt has the width of 0.1–0.5 μm. The surface is clean and without any sheathed amorphous phase. A ripple-like contrast is observed due to the strain resulting from the bending of the belt. In addition, there are some pits on the surface, which may be generated by the high-temperature heat treatment (Figure 6c). HRTEM image taken from the edge area of a NaNbO3 nanobelt reveals that it is structurally uniform single-crystalline phase without any obvious defects and dislocations (Figure 6d). The 2D lattice fringes are oriented approximately 45° from the growth direction. The lattice-resolved image shows the fringes are separated by a distance of about 0.196 nm, which perfectly matches the lattice spacing of the (002) planes (1.959 Å) in the monoclinic NaNbO3 phase.
Those Lindquist ions in Na7(H3O)Nb6O19·14H2O extend along the  direction and build the backbone of the 1D structure. In subsequent calcination stage, the Lindquist units with the edge-sharing Nb–O polyhedra are ruptured to form more stable corner-sharing polyhedron groups. As the transitions mainly involve the breakage of chemical bonds such as Nb–O and rotation of NbO6 octahedra, the temperature as high as 500–550°C is needed to drive rate-limiting diffusion in solid-state phase conversion. It is well known that during the thermal dehydroxylation process, the water molecules are formed and lost between the two adjacent layers of hydroxyl ions. Under the high temperature, the dehydration process occurs quickly (as evidenced by the TG curve in Figure 5a) producing a great many atomic vacancies, which results in low thermal stability of Na7(H3O)Nb6O19·14H2O in the state. Therefore, to minimize the overall system energy and stability the crystal structure, the diffusion of Nb, O, and Na atoms is accelerated. During the structural transformation process, owing to the conventional six-coordinate microstructure, niobium atoms work as central atoms and coordinate with oxygen in the 1D precursor, then many small networks comprising corner-sharing NbO67- units generate as the crystalline nuclei. With the heat treatment process proceeds, a whole rearrangement atomic network is built on pre-existing nuclei in the restricted space of the precursor. That is, a steadier framework of corner-sharing NbO6 octahedra with Na atoms occupying the cavities is generated across the whole volume (Figure 7). This dehydration process requires long-range diffusion of Nb and Na atoms, and this reaction cannot be topochemical. However, in the heat treatment condition, sudden collapse of the precursor nanobelt can be avoided. As a result, the formation of NaNbO3 nanobelt derived from the atomic rearrangement in the crystal structure of Na7(H3O)Nb6O19·14H2O is observed during the decomposition process. It is noteworthy to point out, because of the nanosized diffusion distances for atoms moving between the contact areas, that the wire-like aggregates of Na7(H3O)Nb6O19·14H2O nanobelts can be converted into single-crystalline NaNbO3 nanobelts conveniently under high temperature. Moreover, the high temperature also brings lots of thermal defects in original sublattices, some of which may expand to the surface finally and result in some pits (see the area indicating by arrowhead in Figure 6c).
All the above results reveal that the 1D characteristic of the precursor and the solid-state phase transformation process are all the important factors on the formation of perovskite NaNbO3 nanobelts. The existing 1D nanostructure serves as structural template from which NaNbO3 nanobelt can be readily generated. The size of the precursor is a critical determinant factor in governing the resultant shape of the final NaNbO3 product. Above a critical size, propagation of the reaction front is observed, and the basic morphology of the precursor is maintained . During transformation process of the Na7(H3O)Nb6O19·14H2O nanobelt, the width of the reaction zone is not comparable to the size of this precursor, propagation of the reaction front can span, and the 1D nonequilibrium shape can be maintained. A second vital factor is post-temperature-induced phase transformation that drives oriented rearrangement of NaNbO3 nanoparticles into single-crystalline nanobelts. The precursor undergoes solid-phase reactions rather than continues to grow under hydrothermal circumstance, no dissolution and atom-by-atom recrystallization process happens, which prevents potential shape evolution of the 1D precursor. Therefore, perovskite formation in solution phase can be avoided using short treat time. Increase in reaction time results in lots of NaNbO3 cubes, as shown in Figure 8a. The controllable surface structures are further shown in Figure 8b. When increasing reaction temperature from 150–180 to 200–220°C, stable NaNbO3 perovskite is formed, and no 1D nanostructure is obtained. The higher temperature affords adequate energy to overcome the activation energy and the reaction barrier in the formation of perovskite structure. This also affords a facile way to change the surface structure of niobate films.
We have successfully developed a facile precursor-template route to chemically fabricate dense semi-ordered NaNbO3 nanobelt arrays with tunable aspect ratio, which may be thermodynamically inaccessible structural and morphological features. During the thermal conversion process, atoms gradually rearrange in the restricted space of 1D Na7(H3O)Nb6O19 14H2O precursor until single-crystalline NaNbO3 nanobelt forms without loss of the original shape. The study facilitates to advance the understanding of the crystal phase control and transformation during solid-state reactions. We also established the controlled organization of the film surface with NaNbO3 nanocubes, which may be also useful for optical and piezoelectric devices. The proposed chemical strategy for NaNbO3 film formation may be extended to the fabrication of more niobate arrays.
Boukai AI, Bunimovich Y, Tahir-Kheli J, Yu JK, Goddard WA III, Heath JR: Nature. 2008, 451: 168. 10.1038/nature06458
Bierman MJ, Albert Lau YK, Kvit AV, Schmitt AL, Jin S: Science. 2008, 320: 1060. 10.1126/science.1157131
Yan X, Xu D, Xue D: Acta Mater. 2007, 55: 5747. 10.1016/j.actamat.2007.06.023
Liu J, Xue D: Thin Solid Films. 2009, 517: 4814. 10.1016/j.tsf.2009.03.021
Liu M, Xue D: J Phys Chem C. 2008, 112: 6346. 10.1021/jp800803s
Yan C, Liu J, Liu F, Wu J, Gao K, Xue D: Nanoscale Res Lett. 2008, 3: 473. 10.1007/s11671-008-9193-6
Wang Z, Brust M: Nanoscale Res Lett. 2007, 2: 34. 10.1007/s11671-006-9026-4
Mehta SK, Kumar S, Chaudhary S, Bhasin KK: Nanoscale Res Lett. 2009, 4: 1197. 10.1007/s11671-009-9377-8
Santos A, Vojkuvka L, Pallares J, Ferre-Borrull J, Marsal LF: Nanoscale Res Lett. 2009, 4: 1021. 10.1007/s11671-009-9351-5
Lu P, Xue D: Mod Phys Lett B. 2009, 23: 3835. 10.1142/S0217984909021892
Liu F, Xue D: Surf Rev Lett. 2010, 17: 135. 10.1142/S0218625X10014090
Wu J, Xue D: Mater Res Lett. 2010, 45: 300.
Saito Y, Takao H, Tani T, Nonoyama T, Takatori K, Homma T, Nagaya T, Nakamura M: Nature. 2004, 432: 84. 10.1038/nature03028
Buse K, Adibi A, Psaltis D: Nature. 1998, 393: 665. 10.1038/31429
Xue D, Zhang S: J Phys Condens Matter. 1997, 9: 7515. 10.1088/0953-8984/9/36/002
Xue D, Zhang S: Chem Phys Lett. 1998, 291: 401. 10.1016/S0009-2614(98)00617-4
Liu M, Xue D, Zhang S, Zhu H, Wang J, Kitamura K: Mater Lett. 2005, 59: 1095. 10.1016/j.matlet.2004.12.015
Xue D, Kitamura K: Solid State Commun. 2002, 122: 537. 10.1016/S0038-1098(02)00180-1
Luo C, Xue D: Langmuir. 2006, 22: 9914. 10.1021/la062193v
Shiratori Y, Magrez A, Dornseiffer J, Haegel FH, Pithan C, Waser R: J Phys Chem B. 2005, 109: 20122. 10.1021/jp052974p
Shiratori Y, Magrez A, Fischer W, Pithan C, Waser R: J Phys Chem C. 2007, 111: 18493. 10.1021/jp0738053
Ji L, Liu M, Xue D: Mater Res Bull. 2010, 45: 314. 10.1016/j.materresbull.2009.12.003
Xu J, Xue D: Acta Mater. 2007, 55: 2397. 10.1016/j.actamat.2006.11.032
Alam TM, Nyman M, Cherry BR, Segall JM, Lybarger LE: J Am Chem Soc. 2004, 126: 5610. 10.1021/ja0398159
Nyman M, Bonhomme F, Alam TM, Rodriguez MA, Cherry BR, Krumhansl JL, Nenoff TM, Sattler AM: Science. 2002, 297: 996. 10.1126/science.1073979
Son DH, Hughes SM, Yin YD, Alivisatos AP: Science. 2004, 306: 1009. 10.1126/science.1103755
Financial support from the Natural Science Foundation of China (grant Nos. 50872016, 20973033) is acknowledged.