Patent Application
20120148861
The general preparation of silver nanowires (10-200 aspect ratio) is known. See, for example, Angew. Chem. Int. Ed. 2009, 48, 60, Y. Xia, Y. Xiong, B. Lim, S. E. Skrabalak, which is hereby incorporated by reference in its entirety. Such preparations typically employ Fe2+ or Cu2+ ions to “catalyze” the wire formation over other morphologies. The controlled preparation of silver nanowires having the desired lengths and widths, however, is not known. For example, the Fe2+ produces a wide variety of lengths or thicknesses and the Cu2+ produces wires that are too thick for many applications.
The metal ions used to catalyze wire formation are generally primarily reported to be provided as a metal halide salt, usually as a metal chloride, for example, FeCl2 or CuCl2. See, for example, J. Jiu, K. Murai, D. Kim, K. Kim, K. Suganuma, Mat. Chem. & Phys., 2009, 114, 333, which refers to NaCl, CoCl2, CuCl2, NiCl2 and ZnCl2; Japanese patent application publication JP2009155674, which describes SnCl4; S, Nandikonda, “Microwave Assisted Synthesis of Silver Nanorods,” M. S. Thesis, Auburn University, Aug. 9, 2010, which refers to NaCl, KCl, MgCl2, CaCl2, MnCl2, CuCl2, and FeCl3; S. Nandikonda and E. W. Davis, “Effects of Salt Selection on the Rapid Synthesis of Silver Nanowires,” Abstract INOR-299, 240th ACS National Meeting, Boston, Mass., Aug. 22-27, 2010, which discloses NaCl, KCl, MgCl2, CaCl2, MnCl2, CuCl2, FeCl3, Na2S, and NaI; Chinese patent application publication CN101934377, which discloses Mn2+; Y. C. Lu, K. S. Chou, Nanotech., 2010, 21, 215707, which discloses Pd2+; and Chinese patent application publication CN102029400, which discloses NaCl, MnCl2, and Na2S.
At least some embodiments provide methods comprising providing a composition comprising at least one first reducible metal ion and at least one second metal or metal ion comprising at least one element or ion of an element from IUPAC Group 9 other than iridium or an ion of iridium, the at least one second metal or metal ion differing in atomic number from the at least one first reducible metal ion; and reducing the at least one first reducible metal ion to at least one first metal.
In at least some embodiments, the at least one first reducible metal ion may comprise one or more of at least one coinage metal ion, at least one ion of an element from IUPAC Group 11, or at least one silver ion.
In some cases, the at least one second metal or metal ion may comprise cobalt, an ion of cobalt, rhodium, or an ion of cobalt.
Other embodiments provide the at least one first metal produced according to such methods.
Still other embodiments provide metal nanowires comprising the at least one first metal produced according to such methods. In some cases, the metal nanowires may comprise an aspect ratio between about 50 and about 10,000. Such nanowires may, for example, comprise an average diameter of between about 10 nm and about 300 nm. An exemplary metal nanowire is a silver nanowire.
Yet still other embodiments provide articles comprising the at least one first metal produced according to such methods. Such articles may, for example, comprise at least one of an electronic display, a touch screen, a portable telephone, a cellular telephone, a computer display, a laptop computer, a tablet computer, a point-of-purchase kiosk, a music player, a television, an electronic game, an electronic book reader, a transparent electrode, a solar cell, a light emitting diode, an electronic device, a medical imaging device, or a medical imaging medium.
These embodiments and other variations and modifications may be better understood from the brief description of figures, description, exemplary embodiments, examples, figures, and claims that follow. Any embodiments provided are given only by way of illustrative example. Other desirable objectives and advantages inherently achieved may occur or become apparent to those skilled in the art. The invention is defined by the appended claims.
All publications, patents, and patent documents referred to in this document are incorporated by reference herein in their entirety, as though individually incorporated by reference.
U.S. Provisional Application No. 61/421,298, filed Dec. 9, 2010, entitled METAL ION CATALYSIS OF METAL ION REDUCTION, METHODS, COMPOSITIONS, AND ARTICLES; and U.S. Provisional Application No. 61/488,835, filed May 23, 2011, entitled METAL ION CATALYSIS OF METAL ION REDUCTION, METHODS, COMPOSITIONS, AND ARTICLES, are both hereby incorporated by reference in its entirety.
Some embodiments provide methods comprising reducing at least one reducible metal ion to at least one metal. A reducible metal ion is a cation that is capable of being reduced to a metal under some set of reaction conditions. In such methods, the at least one first reducible metal ion may, for example, comprise at least one coinage metal ion. A coinage metal ion is an ion of one of the coinage metals, which include copper, silver, and gold. Or such a reducible metal ion may, for example, comprise at least one ion of an IUPAC Group 11 element. An exemplary reducible metal ion is a silver cation. Such reducible metal ions may, in some cases, be provided as salts. For example, silver cations might, for example, be provided as silver nitrate.
In such embodiments, the at least one metal is that metal to which the at least one reducible metal ion is capable of being reduced. For example, silver would be the metal to which a silver cation would be capable of being reduced.
These methods are also believed to be applicable to reducible metal cations other than silver cations, including, for example reducible cations of other IUPAC Group 11 elements, reducible cations of other coinage metals, and the like. These methods may also be used to prepare products other than nanowires, such as, for example, nanocubes, nanorods, nanopyramids, nanotubes, and the like. Such products may be incorporated into articles, such as, for example, transparent electrodes, solar cells, light emitting diodes, other electronic devices, medical imaging devices, medical imaging media, and the like.
In some embodiments, the at least one reducible metal ion is reduced in the presence of at least one second metal or metal ion comprising at least one metal or metal ion from IUPAC Group 9 other than iridium or an ion of iridium. Exemplary metals or metal ions from IUPAC Group 9 include cobalt, ions of cobalt, rhodium, and ions of rhodium. Metal ions may be in any oxidation state, such as, for example, +2, +3, +4, +5, or +6.
Applicants have discovered that metals or metal ions from IUPAC Groups 9 other than iridium or ions of iridium may be used to prepare metal nanowires, such as, for example, silver nanowires, with desirable control of thickness, or length, or both, often with improved control of non-wire contamination.
It is notable that Applicants have not been able to prepare silver nanowires using iridium compounds in place of cobalt compounds or rhodium compounds, even though iridium is the next larger member of IUPAC Group 9.
In some embodiments, the metal product formed by such methods is a nanostructure, such as, for example, a one-dimensional nanostructure. Nanostructures are structures having at least one “nanoscale” dimension less than 300 nm. Examples of such nanostructures are nanorods, nanowires, nanotubes, nanopyramids, nanoprisms, nanoplates, and the like. “One-dimensional” nanostructures have one dimension that is much larger than the other two nanoscale dimensions, such as, for example, at least about 10 or at least about 100 or at least about 200 or at least about 1000 times larger.
Such one-dimensional nanostructures may, in some cases, comprise nanowires. Nanowires are one-dimensional nanostructures in which the two short dimensions (the thickness dimensions) are less than 300 nm, preferably less than 100 nm, while the third dimension (the length dimension) is greater than 1 micron, preferably greater than 10 microns, and the aspect ratio (ratio of the length dimension to the larger of the two thickness dimensions) is greater than five. Nanowires are being employed as conductors in electronic devices or as elements in optical devices, among other possible uses. Silver nanowires are preferred in some such applications.
The compositions and methods of the present application allow tailoring of nanowire diameters. In some cases, nanowires may be thin or thick. Thin nanowires can be useful in applications where transparency is important, while thick nanowires can be useful in applications requiring high current densities. Such nanowires may, for example, comprise an average diameter of between about 10 nm and about 300 nm, or of between about 25 nm and about 260 nm.
Such methods may be used to prepare nanostructures other than nanowires, such as, for example, nanocubes, nanorods, nanopyramids, nanotubes, and the like. Nanowires and other nanostructure products may be incorporated into articles, such as, for example, electronic displays, touch screens, portable telephones, cellular telephones, computer displays, laptop computers, tablet computers, point-of-purchase kiosks, music players, televisions, electronic games, electronic book readers, transparent electrodes, solar cells, light emitting diodes, other electronic devices, medical imaging devices, medical imaging media, and the like.
A common method of preparing nanostructures, such as, for example, nanowires, is the “polyol” process. Such a process is described in, for example, Angew. Chem. Int. Ed. 2009, 48, 60, Y. Xia, Y. Xiong, B. Lim, S. E. Skrabalak, which is hereby incorporated by reference in its entirety. Such processes typically reduce a metal cation, such as, for example, a silver cation, to the desired metal nanostructure product, such as, for example, a silver nanowire. Such a reduction may be carried out in a reaction mixture that may, for example, comprise one or more polyols, such as, for example, ethylene glycol (EG), propylene glycol, butanediol, glycerol, sugars, carbohydrates, and the like; one or more protecting agents, such as, for example, polyvinylpyrrolidinone (also known as polyvinylpyrrolidone or PVP), other polar polymers or copolymers, surfactants, acids, and the like; and one or more metal ions. These and other components may be used in such reaction mixtures, as is known in the art. The reduction may, for example, be carried out at one or more temperatures from about 120° C. to about 190° C., or from about 80° C. to about 190° C.
U.S. Provisional Application No. 61/421,298, filed Dec. 9, 2010, entitled METAL ION CATALYSIS OF METAL ION REDUCTION, METHODS, COMPOSITIONS, AND ARTICLES, which is hereby incorporated by reference in its entirety, disclosed the following 27 non-limiting exemplary embodiments:
A. A method comprising:
providing a composition including:
U.S. Provisional Application No. 61/488,835, filed May 23, 2011, entitled METAL ION CATALYSIS OF METAL ION REDUCTION, METHODS, COMPOSITIONS, AND ARTICLES, disclosed the following 27 non-limiting exemplary embodiments:
AD. A method comprising:
providing a composition comprising:
reducing the at least one first reducible metal ion to at least one first metal.
AE. The method of embodiment AD, wherein the composition further comprises at least one protecting agent.
AF. The method of embodiment AE, wherein the at least one protecting agent comprises at least one of: one or more surfactants, one or more acids, or one or more polar polymers.
AG. The method of embodiment AE, wherein the at least one protecting agent comprises polyvinylpyrrolidinone.
AH. The method of embodiment AE 2, further comprising inerting the at least one protecting agent.
AJ. The method of embodiment AD, wherein the at least one first reducible metal ion comprises at least one coinage metal ion.
AK. The method of embodiment AD, wherein the at least one first reducible metal ion comprises at least one ion of an element from IUPAC Group 11.
AL. The method of embodiment AD, wherein the at least one first reducible metal ion comprises at least one ion of silver.
AM. The method of embodiment AD, wherein the at least one first compound comprises silver nitrate.
AN. The method of embodiment AD, wherein the at least one second compound comprises at least one salt of said at least one second metal or metal ion.
AP. The method of embodiment AN, wherein the at least one salt comprises at least one chloride.
AQ. The method of embodiment AD, wherein the at least one second compound comprises rhodium(III) chloride trihydrate.
AR. The method of embodiment AD, wherein the at least one solvent comprises at least one polyol.
AS. The method of embodiment AD, wherein the at least one solvent comprises at least one of: ethylene glycol, propylene glycol, glycerol, one or more sugars, or one or more carbohydrates.
AT. The method of embodiment AD, wherein the composition has a ratio of the total moles of the at least one second metal or metal ion to the total moles of the at least one first reducible metal ion from about 0.0001 to about 0.1.
AU. The method of embodiment AD, wherein the reduction is carried out at one or more temperatures from about 120° C. to about 190° C.
AV. The method of embodiment AD, further comprising inerting one or more of: the composition, the at least one compound comprising the at least one first reducible metal ion, the at least one second metal or metal ion, or the at least one solvent.
AW. The at least one first metal produced according to the method of embodiment AD.
AX. At least one article comprising the at least one first metal produced according to the method of embodiment AD.
AY. The at least one article of embodiment AX, wherein the at least one first metal comprises one or more nanowires, nanocubes, nanorods, nanopyramids, or nanotubes.
AZ. The at least one article of embodiment AX, wherein the at least one first metal comprises at least one object having an average diameter of between about 10 nm and about 500 nm.
BA. The at least one article of embodiment AX, wherein the at least one first metal comprises at least one object having an aspect ratio from about 50 to about 10,000.
BB. At least one metal nanowire with an average diameter of between about 10 nm and about 150 nm, and with an aspect ratio from about 50 to about 10,000.
BC. The nanowire of embodiment BB, wherein the at least one metal nanowire comprises at least one coinage metal.
BD. The nanowire of embodiment BB, wherein the at least one metal nanowire comprises at least one element of IUPAC Group 11.
BE. The nanowire of embodiment BB, wherein the at least one metal nanowire comprises silver.
BF. At least one article comprising the at least one metal nanowire of embodiment BB.
To a 500 mL reaction flask was added 280 mL ethylene glycol (EG) and 1.1 g of 7.4 mM CoCl2.2H2O in EG. This solution was stripped of at least some dissolved gases by bubbling N2 into the solution for at least 2 hrs using a glass pipette at room temperature with mechanical stirring while at 100 rpm. (This operation will be referred to as “degassing” the solution in the sequel.) Stock solutions of 0.25 M AgNO3 in EG and 0.77 M polyvinylpyrrolidinone (PVP) in EG were also degassed by bubbling N2 into the solutions for 60 minutes. Two syringes were loaded with 20 mL each of the AgNO3 and PVP solutions. The reaction mixture was heated to 145° C. under N2 and the AgNO3 and PVP solutions were added at a constant rate over 25 minutes via 12 gauge TEFLON® fluoropolymer syringe needles. The reaction mixture was held at 145° C. for 90 minutes then allowed to cool to room temperature. From the cooled mixture, the reaction mixture was diluted by an equal volume of acetone, and centrifuged at 500 G for 45 minutes. The decanted solid was re-dispersed in 200 mL isopropanol, shaken 10 minutes and centrifuged again, decanted and diluted with 15 mL isopropanol.
The procedure of Example 1 was repeated, using 7.0 g of 7.4 mM CoCl2.2H2O in EG. The nanowires had an average diameter of 63±14 nm and an average length of 11±5.0 μm, based on measurement of at least 100 wires.
The procedure of Example 1 was repeated, using 5.6 g of 7.4 mM CoCl2.2H2O in EG and 4.3 g of freshly prepared 32 mM Co(NO3)2 in EG. The reaction was carried out at 155° C. The nanowires had an average diameter of 62±18 nm and an average length of 20±5.2 μm, based on measurement of at least 100 wires.
The procedure of Example 3 was repeated, using 9.8 mg of rhodium (III) chloride trihydrate.
An optical micrograph of the silver nanowire product is shown in
To a 500 mL reaction flask was added 280 mL ethylene glycol (EG) and 1.4 g of a freshly prepared 15 mM IrCl3.3H2O dispersion in EG. This solution was degassed for 2 hrs by bubbling N2 into the solution using a glass pipette at room temperature with mechanical stirring while at 100 rpm. Stock solutions of 0.25 M AgNO3 in EG and 0.84 M polyvinylpyrrolidinone (PVP) in EG were also degassed by bubbling N2 into the solutions for at least 60 minutes. Two syringes were loaded with 20 mL each of the AgNO3 and PVP solutions. The reaction mixture was heated to 155° C. under N2 and the AgNO3 and PVP solutions were added at a constant rate over 25 minutes via 12 gauge TEFLON® fluoropolymer syringe needles. The reaction was held at 155° C. for 90 minutes then allowed to cool to room temperature.
The procedure of Example 5 was repeated, using 2.9 g of a freshly prepared 7.0 mM dispersion of K2IrCl6 in EG, instead of the IrCl3.3H2O dispersion. The reaction was carried out at 145° C., instead of 155° C.
The procedure of Example 5 was repeated, using 2.3 g of a freshly prepared 7.0 mM dispersion of InCl3.4H2O in EG, instead of the IrCl3.3H2O dispersion.
To a 100 mL reaction flask was added 50 mL ethylene glycol (EG) and 0.29 g of 7.0 mM AuCl3 in EG. This solution was degassed for 2 hrs by bubbling N2 into the solution using a glass pipette at room temperature with mechanical stirring while at 100 rpm. Stock solutions of 0.25 M AgNO3 in EG and 0.84 M polyvinylpyrrolidinone (PVP) in EG were also degassed by bubbling N2 into the solutions for at least 60 minutes. Two syringes were loaded with 3 mL each of the AgNO3 and PVP solutions. The reaction mixture was heated to 145° C. under N2 and the AgNO3 and PVP solutions were added at a constant rate over 25 minutes via 20 gauge TEFLON® fluoropolymer syringe needles. The reaction was held at 145° C. for 150 minutes then allowed to cool to room temperature.
Samples taken after 15, 30, 60, 90, 120, and 150 min of reaction appeared to have only nanoparticles, but no nanowires.
The invention has been described in detail with reference to particular embodiments, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention. The presently disclosed embodiments are therefore considered in all respects to be illustrative and not restrictive. The scope of the invention is indicated by the appended claims, and all changes that come within the meaning and range of equivalents thereof are intended to be embraced within.
This application claims the benefit of U.S. Provisional Application No. 61/421,298, filed Dec. 9, 2010, entitled METAL ION CATALYSIS OF METAL ION REDUCTION, METHODS, COMPOSITIONS, AND ARTICLES; and U.S. Provisional Application No. 61/488,835, filed May 23, 2011, entitled METAL ION CATALYSIS OF METAL ION REDUCTION, METHODS, COMPOSITIONS, AND ARTICLES; each of which is hereby incorporated by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 61421298 | Dec 2010 | US | |
| 61488835 | May 2011 | US |
