Patent Application
20070183964
The present invention relates to microstructures comprising transition metal chalcogenide crystals. The present invention particularly relates to a microstructure comprising transition metal dichalcogenide crystals and a method for preparing microstructures. The microstructure can be used for various applications such as electromagnetic measuring instruments because of its unique properties.
Transition metal chalcogenides have a common crystal structure and various unique properties such as large electrical, magnetic, and optical anisotropy; hence, the investigation of their properties and the development of their applications have been attracting much attention. In particular, V group transition metal dichalcogenides such as NbSe2 and TaS2 have been intensively investigated for applications and properties such as superconductivity and low-dimensional anisotropy.
In particular, in order to determine their properties and in order to develop their applications based on the obtained properties, the dichalcogenides must be processed or formed into structures having such a crystal texture that their properties can be exhibited.
In order to obtain, for example, a superconducting quantum interface device (SQUID) using the superconductivity of transition metal chalcogenide, structures must be prepared so as to have a crystal texture topologically equivalent to that of the chalcogenide.
The inventors have proposed methods for preparing microstructures with a crystal texture equivalent to that of transition metal chalcogenide as disclosed in below Patent Document 1 and Non-patent Documents 1 and 2.
Known Technical Documents
Patent Document 1: Japanese Unexamined Patent Application Publication No. 2002-255699
Non-patent Document 1: Satoshi TANDA, Taku TSUNETA, Yoshitoshi OKAJIMA, Katsuhiko INAGAKI, Kazuhiko YAMAYA, and Noriyuki HATAKENAKA, “A Möbius strip of single crystals”, Nature, Nature Japan K. K., vol. 417, no. 6887 (May 23, 2002), pp. 397-398.
Non-patent Document 2: Satoshi TANDA and Taku TSUNETA, “Topological Materials”, Kotai Butsuri, vol. 37, no. 8 (Aug. 15, 2002), pp. 17-26.
Patent Document 2 discloses a method for preparing a polycrystalline thin-film expected to be applied to solar cells and solid lubricants. This method is a technique for forming a membranous structure made of transition metal chalcogenide.
Patent Document 2: Japanese Unexamined Patent Application Publication No. 7-69782
In order to develop applications of transition metal chalcogenide and V group transition metal dichalcogenide such as NbSe2, nanostructures having a nano-crystal texture and various shapes must be prepared constantly and efficiently.
The present invention provides a nanofiber or nanotube comprising V group transition metal dichalcogenide crystals. In the nanofiber or nanotube, the V group transition metal is Nb or Ta and the chalcogen element is Se or S.
A method for preparing nanofibers or nanotubes comprising V group transition metal dichalcogenide crystals includes a step of producing dichalcogenide by heating a V group transition metal and chalcogen element mixed in a ratio of MX2 in a vacuum to perform a reaction by a chemical transport process. The reaction is performed for a predetermined time under such non-equilibrium conditions that the maximum temperature is about 800° C., the temperature gradient is 1 to 3 deg/cm, and the difference in temperature due to the temperature gradient is 60 to 100 deg. In the nanofiber- or nanotube-preparing method, the V group transition metal is Nb or Ta and the chalcogen element is Se or S.
Alternatively, nanofibers or nanotubes comprising V group transition metal dichalcogenide crystals are prepared in such a manner that C60 acting as a promoter is used in a step of forming dichalcogenide crystals from powdery V group transition metal dichalcogenide that is a starting material by a chemical transport process using iodine acting as a medium. In the preparation of the nanofibers or nanotubes comprising the V group transition metal dichalcogenide crystals, the V group transition metal is Nb or Ta and the chalcogen element is Se or S.
Transition metal trichalcogenide MX3 is a material with strong one-dimensionality due to its crystal structure. It has been known that ribbon- or whisker-shaped narrow crystals that are very narrow and fine can be prepared by allowing components thereof to react with each other by a chemical vapor transport process. The inventors have found that when fine NbSe3 whiskers are formed in such a manner that Se with a low boiling point is repeatedly vaporized and condensed by controlling the atmosphere in a reaction vessel during the formation of such NbSe3 whiskers by the vapor-phase reaction of Nb with Se and NbSe3 molecules formed by the reaction are gathered in one place and then crystallized, the NbSe2 molecules are adsorbed on Se droplets formed in the atmosphere to form loops wound around the droplets acting as templates so that topological crystals with a ring shape, a Mobius strip shape, or an 8-shape are formed. The inventors have reported the finding in Non-patent Documents 1 and 2 described above (Japanese Patent Application No. 2002-340094).
On the other hand, transition metal dichalcogenide MX2 has a crystal structure in which triangular prism-shaped repeating units identical to those of MX3 are linked to each other to form a two-dimensional arrangement similar to that of graphite. Its properties such as low-dimensional anisotropy are attracting much attention because of such a structure. In a known chemical transport process, although powdery fine crystals can be prepared depending on the percentage of MX2 by a vapor-phase reaction, the crystals have hexagonal faces due to its crystal structure.
From the fact that the MX3 whiskers are formed during the formation of the reported MX3 topological material, the inventors have conceived that MX2 nanofibers and MX2 nanotubes can be prepared by controlling reaction conditions for the formation of MX2 using MX3 nanofibers, partly formed in an atmosphere, acting as templates.
That is, features of the present invention are based on the discovery of a phenomenon that MX3 is converted to MX2.
When starting materials mixed in a ratio of MX2 are allowed to react with each other, NbSe3 is primarily produced due to the temperature gradient in a reaction atmosphere and then converted into NbSe2 because the temperature at which NbSe3 is produced is 740° C. and is less than the temperature at which NbSe2 is produced, NbSe2 being produced at 800° C.
When NbSe3 is converted into NbSe2 during the removal of selenium, NbSe2 nanofibers and nanotubes are formed with nano-sized fibril structures acting as templates.
When MX2 that is a starting material, iodine, and C60 are subjected to a reaction in such a manner that MX2, iodine, and C60 are placed in a quartz tube and the quartz tube is evacuated and then sealed, MX2 is partially converted into MX3, which is readily vaporizable, at a temperature of 700° C. to 720° C. during heating, whereby MX3 nanofibers are primarily formed. In this step, portions of the inner wall of the quartz tube and C60 molecules act as nuclei for growing the nanofibers, that is, C60 acts as a promoter for producing the nanofibers. The C60 molecules act as nuclei for growing MX3 filaments or nanofibers as disclosed in Japanese Unexamined Patent Application Publication No. 2002-255699. After further heating, MX3 is converted into MX2 at a maximum temperature of 780° C. to 820° C. In this step, MX2 nanofibers or nanotubes are formed in a self-assembled manner with the MX3 nanofibers acting as templates.
NbSe2 is spherically formed around C60. Initial nanoparticles surrounding each C60 molecule form nanorings, which grow into nanotubes. Other nanoparticles surrounding no C60 molecule grow into nanofibers.
That is, trichalcogenide nanofibers are primarily formed and dichalcogenide nanofibers and/or nanotubes are then formed.
During the removal of selenium, layered NbSe2 flat structures similar to graphite are curved so as to form tubes, whereby NbSe2 nanotubes similar to carbon nanotubes are prepared.
Nanofibers or nanotubes comprising V group transition metal dichalcogenide crystals are nanomaterials prepared by a chemical transport process described below. A typical nanofiber has a diameter of 5 to 500 nm and a length of 1 to 10 μm. A typical nanotube has substantially the same size as described above although the size thereof varies depending on the multi-wall structure thereof.
These nanomaterials have properties identical to those of bulk single crystals of dichalcogenide as described below. Applications utilizing their properties due to their nanostructure have been expected.
High-purity (99.99%) niobium and selenium, which are starting materials, are weighed in a ratio of MX2. These materials are placed into a quartz ampoule (a length of 20 to 25 cm), heated at a vacuum of 10−6 Torr, allowed to react with each other at a maximum temperature of 820° C. for 72 hours with a temperature gradient of 1 to 3 deg/cm, and then cooled to room temperature, whereby nanomaterials are obtained.
If the reaction time is short, for example, less than one hour, nanofibers or nanotubes can be produced. The reaction is continued for three days at the maximum such that the yield of the nanotubes is increased, though the number of walls of the nanotubes varies depending on the reaction time. The nanotubes prepared in this manner are multi-walled and thick.
Powdery 99.99% NbSe2, which is a starting material, C60, and iodine are placed into a quartz tube. The tube is sealed, evacuated, and then heated.
As well known, the following chemical equilibrium holds in the reaction tube:
MX2+I2⇄MI2+2X
During heating, at 700° C. to 720° C., NbSe2 is partially converted into NbSe3, which is readily vaporizable, whereby crystals are grown with C60 molecules, vaporized at 340° C., acting as growth promoters. NbSe3 nanostructures are grown with the C60 molecules acting as nuclei and then converted into NbSe2 nanostructures at a maximum temperature of about 820° C.
These reaction conditions are substantially the same as those of the above method for directly preparing the transition metal dichalcogenide nanotubes from those starting materials by the chemical transport process.
In the reaction tube, MX2, that is, the NbSe2 nanomaterials are crystallized on low-temperature regions of the quartz ampoule with the above temperature gradient because MI2 is more volatile than MX2.
The NbSe2 nanomaterials obtained are suspended in dichloroethane or isopropyl alcohol and nanoparticles are separated by precipitation.
The nanomaterials can be more properly prepared by this method as compared to that method using the direct reaction.
The nanomaterials prepared by these methods were observed with a scanning electron microscope (SEM), a field emission-transmission electron microscope (FE-TEM), or a scanning ion microscope (SIM) and the structure thereof was investigated as described below.
A transition metal dichalcogenide fiber with a nano-scale extends along a normal NbSe2 crystal with a hexagonal face.
A linear material located at the center of the image is a typical NbSe2 nanofiber having a width of 15 nm and a length of 1 μm. Fine particles that are in contact with the nanotube and a large polygonal plate located in the upper right corner of the image are typical NbSe2 crystals.
In the preparation method using C60 for promoting the formation of the nanofibers/nanotubes, when C60 is present in a reaction step of forming crystals by the chemical transport process using iodine and NbSe2 prepared in advance, C60 acts to form nuclei for forming the nanofibers or the nanotubes, that is, C60 acts as a growth promoter for promoting the formation of the nanofibers or the nanotubes.
Nanoparticles which have such nuclei and which surround each C60 molecule form nanorings, which grow into the nanotubes. However, if wrapping does not occur, the nanofibers grow.
Since C60 is sublimated at 340° C. or more, the formation of the nuclei in the presence of C60 occurs not only on the inner wall of the quartz ampoule but also in the entire inside of the ampoule.
Since the reaction of NbSe2 proceeds in the presence of a large number of the nuclei, NbSe2 nanostructures formed as a result of the competition are fine. Fluctuation in a vapor phase reaction allows formed crystals to have a spiral structure.
As described above, it has been confirmed that C60 plays a critical role in the growth of the NbSe2 nanostructures and the preparation efficiency and yield thereof can be enhanced by the use of C60.
Properties of nanomaterials prepared by these methods were investigated. A NbSe2 nanofiber was attached to an electrode by a focus ion beam technique and then measured for electrical properties. The electrical resistance in a crystal plane was 7×10−5 Ω·cm.
Measurement was performed in such a manner that the tip of an atomic force microscope (AFM) was used an electrode and directly placed on a sample. A conductive probe was a silicon single crystal coated with platinum.
NbSe2 fibers were ultrasonically mixed in isopropyl alcohol and then deposited on an indium film with a thickness of 200 nm.
The efficiency of this system was tested using a multi-walled carbon nanotube and it was confirmed that the electrical resistance thereof agreed with values disclosed in ordinary scientific documents.
In order to perforate the outermost insulating wall, a load of 200 nN was applied to the tip of the AFM, whereby a current of 5×10−9 A was allowed to flow with a bias voltage of 1×10−3 V. That is, the resistance is about 200 kΩ and the resistivity is roughly estimated to be in the range of 10−3 to 10−2 Ω·m. This value is close to the resistivity perpendicular to the c axis, that is, 4×10−5 Ω·m.
Electrical properties of these nanomaterials are substantially the same as those of bulk crystals, that is, the properties thereof are maintained. NbSe2 exhibits superconductivity at 5 K and a CDW transition at 30 K. TaSe2 exhibits a CDW transition at room temperature (300 K).
In the above description, Nb which is a V group transition metal and Se which is a chalcogen element are used; however, a V group transition metal and chalcogen element used herein are not limited to these elements. From properties common to these elements, it is clear that nanofibers or nanotubes can be theoretically prepared from another V group transition metal and another chalcogen element by the same method as described above. In particular, TaS2 consisting of Ta which is a V group transition metal and S which is a chalcogen element is useful in preparing nanomaterial identical to those described above under substantially the same conditions as described above.
The present invention provides a nanofiber and nanotube made of V group transition metal dichalcogenide, for example, Nb or Ta dichalcogenide and also provides an efficient preparation method thereof. This enables the investigation of unknown characteristics of a group of these materials having specific properties and also enables the development of applications of these materials.
Any nanomaterial provided by the present invention is essential to advances in techniques using properties thereof because the nanomaterial has a topological structure for exhibiting its properties; hence, the nanomaterial contributes to the progress of industry.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2003-156227 | Jun 2003 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP04/04559 | 3/30/2004 | WO | 12/21/2006 |
