EP2916981A1 - Method for preparing a silver nanowire - Google Patents
Method for preparing a silver nanowireInfo
- Publication number
- EP2916981A1 EP2916981A1 EP13776920.4A EP13776920A EP2916981A1 EP 2916981 A1 EP2916981 A1 EP 2916981A1 EP 13776920 A EP13776920 A EP 13776920A EP 2916981 A1 EP2916981 A1 EP 2916981A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- silver
- nanowires
- silver nitrate
- propylene glycol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 44
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 239000002042 Silver nanowire Substances 0.000 title claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 87
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims abstract description 63
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 59
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229910001961 silver nitrate Inorganic materials 0.000 claims abstract description 28
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims abstract description 23
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims abstract description 23
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims abstract description 23
- 235000019270 ammonium chloride Nutrition 0.000 claims abstract description 14
- 238000010438 heat treatment Methods 0.000 claims description 15
- 239000002070 nanowire Substances 0.000 abstract description 17
- -1 silver cations Chemical class 0.000 abstract description 8
- 229910052709 silver Inorganic materials 0.000 abstract description 7
- 239000004332 silver Substances 0.000 abstract description 7
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 abstract description 4
- 229940054334 silver cation Drugs 0.000 abstract description 4
- 229960004063 propylene glycol Drugs 0.000 description 19
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- 239000002086 nanomaterial Substances 0.000 description 14
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 229910021645 metal ion Inorganic materials 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 238000005259 measurement Methods 0.000 description 6
- 229920005862 polyol Polymers 0.000 description 5
- 150000003077 polyols Chemical class 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000007792 addition Methods 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000002059 diagnostic imaging Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000002073 nanorod Substances 0.000 description 2
- 239000002071 nanotube Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002055 nanoplate Substances 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/16—Making metallic powder or suspensions thereof using chemical processes
- B22F9/18—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
- B22F9/24—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/05—Metallic powder characterised by the size or surface area of the particles
- B22F1/054—Nanosized particles
- B22F1/0547—Nanofibres or nanotubes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/05—Metallic powder characterised by the size or surface area of the particles
- B22F1/054—Nanosized particles
- B22F1/0553—Complex form nanoparticles, e.g. prism, pyramid, octahedron
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C5/00—Alloys based on noble metals
- C22C5/06—Alloys based on silver
Definitions
- polyol processes in which a silver salt is heated in a polyol (typically ethylene glycol (EG)) in the presence of polyvinylpyrrolidinone (PVP, also known as polyvinylpyrrolidone), yielding a suspension of AgNW in EG, from which the wires can be isolated and/or purified as desired.
- EG ethylene glycol
- PVP polyvinylpyrrolidinone
- US patent application publication 2012/0063948A discloses reduction of silver nitrate in the presence of ammonium chloride.
- Some embodiments provide methods to prepare silver nanowires comprising at least two stages.
- At least a first stage provides a first composition comprising 1,2- propylene glycol, polyvinylpyrrolidone (PVP), and ammonium chloride.
- PVP polyvinylpyrrolidone
- the PVP has weight average molecular weight greater than about 15,000 g/mol, or between about 40,000 and about 60,000 g/mol, or about 50,000 g/mol.
- the first composition is preferably provided at a temperature less than about 140 °C, or between about 80 °C and about 120 °C, or about 90 °C.
- a second composition comprising 1,2- propylene glycol and silver nitrate is added to the first composition over a time period that is at least about 16 hrs, or between about 20 hrs and about 28 hrs, or about 24 hrs, during which time at least some of the silver nitrate is reduced to silver nanostructures, such as, for example, silver nanowires.
- Silver nanowires are a unique and useful wire-like form of the metal in which the two short dimensions (the thickness dimensions) are less than 300 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. They are being examined as conductors in electronic devices or as elements in optical devices, among other possible uses.
- 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.
- 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.
- 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.
- silver cations might, in some cases, be provided as silver nitrate.
- the at least one metal is that metal to which the at least one reducible metal ion is capable of being reduced.
- silver would be the metal to which a silver cation would be capable of being reduced.
- a common method of preparing nanostructures 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.
- Applicants have observed that reproducibility can be improved and variability reduced if such metal cation reduction is carried out in at least two stages.
- a first stage or stages provides a first composition comprising 1,2- propylene glycol, polyvinylpyrrolidone (PVP), and ammonium chloride.
- PVP polyvinylpyrrolidone
- the first composition is preferably provided at a temperature less than about 140 °C, or between about 80 °C and about 120 °C, or about 90 °C.
- the components of the first composition are contacted with each other prior to heating.
- the first stage or stages may provide the first composition in a series of sub-stages each providing some of the components of the composition. Some of the components may be provided in more than one sub-stage.
- the first composition may further comprise silver nitrate.
- a first portion of the first composition may be provided comprising silver nitrate, followed by a second portion of the first composition comprising ammonium chloride.
- a second composition comprising 1,2- propylene glycol and silver nitrate is added to the first composition over a time period that is at least about 16 hrs, or between about 20 hrs and about 28 hrs, or about 24 hrs, during which time at least some of the silver nitrate is reduced to silver nanostructures, such as, for example, silver nanowires.
- the metal product formed by such methods is a nanostructure, such as, for example, a one-dimensional nano structure.
- Nanostructures are structures having at least one "nanoscale" dimension less than 300 nm, and at least one other dimension being much larger than the nanoscale dimension, 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.
- nanoscale dimension 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.
- 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 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.
- 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.
- 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 method comprising:
- composition the adding occurring over the course of at least about 16 hrs, and the at least one second composition comprising 1,2-propylene glycol and silver nitrate;
- composition the at least one fourth composition comprising ammonium chloride.
- At least one third composition comprising polyvinyl pyrrolidone; forming at least one fourth composition by adding at least one fifth composition to the at least one third composition, the at least one fifth
- composition comprising silver nitrate
- composition the at least one sixth composition comprising ammonium chloride.
- Example 1 The procedure of Example 1 was repeated, changing the time period for AgN0 3 solution addition from 64 h to 24 h.
- the resulting silver nanowires had an average diameter of 44.11 nm and average length of 16.7 ⁇ , based on measurement of at least 100 nanowires.
- Example 1 The procedure of Example 1 was repeated, changing the time period for AgN0 3 solution addition from 64 h to 67.3 h, and changing the reaction temperature from 90 °C to 75 °C.
- the resulting silver nanowires had an average diameter of 57.2 nm and average length of 20.5 ⁇ , based on measurement of at least 100 nanowires.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nanotechnology (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Metallurgy (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Composite Materials (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Powder Metallurgy (AREA)
Abstract
Methods of preparing silver nanowires by reducing silver cations are disclosed and claimed, where the silver cation reduction occurs in at least two stages. Such methods can exhibit improved reproducibility and reduced variability. For example the following method can be provided, which comprises the followig steps: providing at least one first composition comprising 1,2-propylene glycol, polyvinyl pyrrolidone, and ammonium chloride; adding at least one second composition to the at least one first composition, the adding occurring over the course of at least about 16 hrs, and the at least one second composition comprising 1,2-propylene glycol and silver nitrate; and reducing at least a portion of the silver nitrate to silver nanowires. The such produced nanowires are useful in, for example, electronics applications.
Description
METHOD FOR PREPARING A SILVER NANOWIRE
BACKGROUND
The general preparation of silver nanowires (AgNW, 10-200 aspect ratio) from silver ions is known. See, for example, Y. Xia, et al., Angew. Chem. Int. Ed. 2009, 48, 60, and J. Jiu, et al., Mat. Chem. & Phys., 2009, 114, 333, each of which is hereby incorporated by reference in its entirety. These include the "polyol" process, in which a silver salt is heated in a polyol (typically ethylene glycol (EG)) in the presence of polyvinylpyrrolidinone (PVP, also known as polyvinylpyrrolidone), yielding a suspension of AgNW in EG, from which the wires can be isolated and/or purified as desired.
Methods of preparing silver nanowires from silver salts are known, where the salt is added to the reaction mixture in more than one step. See, for example, US patent 8,052,773, US patent application publication 2011/0174190, Chinese patent application publication 1740405 A, and Chinese patent
100342064C.
US patent application publication 2012/0063948A discloses reduction of silver nitrate in the presence of ammonium chloride.
SUMMARY
Some embodiments provide methods to prepare silver nanowires comprising at least two stages.
At least a first stage provides a first composition comprising 1,2- propylene glycol, polyvinylpyrrolidone (PVP), and ammonium chloride. The PVP has weight average molecular weight greater than about 15,000 g/mol, or between about 40,000 and about 60,000 g/mol, or about 50,000 g/mol. The first composition is preferably provided at a temperature less than about 140 °C, or between about 80 °C and about 120 °C, or about 90 °C.
In at least one second stage, a second composition comprising 1,2- propylene glycol and silver nitrate is added to the first composition over a time period that is at least about 16 hrs, or between about 20 hrs and about 28 hrs, or
about 24 hrs, during which time at least some of the silver nitrate is reduced to silver nanostructures, such as, for example, silver nanowires.
These and other embodiments may be understood from the description, exemplary embodiments, examples, and claims that follow.
DESCRIPTION
All publications, patents, and patent documents referred to in this document are incorporated by reference herein in there entirety, as though individually incorporated by reference.
U. S. Patent Application No. 61/723,942, filed November 8, 2012, entitled NANOWIRE PREPARATION METHODS, COMPOSITIONS, AND ARTICLES, is hereby incorporated by reference in its entirety.
Introduction
Silver nanowires (AgNW) are a unique and useful wire-like form of the metal in which the two short dimensions (the thickness dimensions) are less than 300 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. They are being examined as conductors in electronic devices or as elements in optical devices, among other possible uses.
A number of procedures have been presented for the preparation of AgNW. See, for example, Y. Xia, et al. (Angew. Chem. Int. Ed. 2009, 48, 60), which is hereby incorporated by reference in its entirety. These include the "polyol" process, in which a silver salt is heated in a polyol (typically ethylene glycol (EG)) in the presence of polyvinylpyrrolidinone (PVP, also known as polyvinylpyrrolidone), yielding a suspension of AgNW in EG, from which the wires can be isolated and/or purified as desired.
Reducible Metal Ions and Metal Products
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, in some cases, 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.
Preparation Methods and Materials
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. Applicants have observed that reproducibility can be improved and variability reduced if such metal cation reduction is carried out in at least two stages.
A first stage or stages provides a first composition comprising 1,2- propylene glycol, polyvinylpyrrolidone (PVP), and ammonium chloride. The PVP has weight average molecular weight greater than about 15,000 g/mol, or between about 40,000 and about 60,000 g/mol, or about 50,000 g/mol. The first composition is preferably provided at a temperature less than about 140 °C, or between about 80 °C and about 120 °C, or about 90 °C.
In some embodiments, the components of the first composition are contacted with each other prior to heating. In some embodiments, the first stage or stages may provide the first composition in a series of sub-stages each
providing some of the components of the composition. Some of the components may be provided in more than one sub-stage.
In at least some embodiments, the first composition may further comprise silver nitrate. For example, a first portion of the first composition may be provided comprising silver nitrate, followed by a second portion of the first composition comprising ammonium chloride.
In a second stage or stages, a second composition comprising 1,2- propylene glycol and silver nitrate is added to the first composition over a time period that is at least about 16 hrs, or between about 20 hrs and about 28 hrs, or about 24 hrs, during which time at least some of the silver nitrate is reduced to silver nanostructures, such as, for example, silver nanowires.
Nanostructures and Nanowires
In some embodiments, the metal product formed by such methods is a nanostructure, such as, for example, a one-dimensional nano structure.
Nanostructures are structures having at least one "nanoscale" dimension less than 300 nm, and at least one other dimension being much larger than the nanoscale dimension, 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. 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 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.
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.
EXEMPLARY EMBODIMENTS
U. S. Patent Application No. 61/723,942, filed November 8, 2012, entitled NANOWIRE PREPARATION METHODS, COMPOSITIONS, AND ARTICLES, which is hereby incorporated by reference in its entirety, disclosed the following twelve non-limiting exemplary embodiments:
A. A method comprising:
providing at least one first composition comprising 1,2-propylene glycol, polyvinyl pyrrolidone, and ammonium chloride;
adding at least one second composition to the at least one first
composition, the adding occurring over the course of at least about 16 hrs, and the at least one second composition comprising 1,2-propylene glycol and silver nitrate; and
reducing at least a portion of the silver nitrate to silver nanowires.
B. The method according to embodiment A, further comprising heating the at least one first composition to a temperature less than about 140 °C.
C. The method according to embodiment A, further comprising heating the at least one first composition to a temperature between about 80 °C and about
120 °C.
D. The method according to embodiment A, further comprising heating the at least one first composition to a temperature of about 90 °C.
E. The method according to embodiment A, wherein the at least one first composition further comprises silver nitrate.
F. The method according to embodiment E, wherein providing the at least one first composition comprises:
providing at least one third composition comprising silver nitrate; and adding at least one fourth composition to the at least one third
composition, the at least one fourth composition comprising ammonium chloride.
G. The method according to embodiment E, wherein providing the at least one first composition comprises:
providing at least one third composition comprising polyvinyl pyrrolidone; forming at least one fourth composition by adding at least one fifth composition to the at least one third composition, the at least one fifth
composition comprising silver nitrate; and
adding at least one sixth composition to the at least one fourth
composition, the at least one sixth composition comprising ammonium chloride.
H. The method according to embodiment G, further comprising heating the at least one third composition to a temperature less than about 140 °C.
J. The method according to embodiment G, further comprising heating the at least one third composition to a temperature between about 80 °C and about 120 °C.
K. The method according to embodiment G, further comprising heating the at least one third composition to a temperature of about 90 °C.
L. The method according to embodiment A, wherein the adding the at least one second composition to the at least one first composition occurs over the course of between about 20 hrs and about 28 hrs.
M. The method according to embodiment A, wherein the adding the at least one second composition to the at least one first composition occurs over the course of about 24 hrs.
EXAMPLES
Example 1
To a 500 mL reaction vessel was charged 430 mL propylene glycol, 7.2 g of polyvinylpyrrolidone (50,000 weight average molecular weight), and 2 mL of a 1 wt % solution of ammonium chloride in propylene glycol. The
mixture was stirred under nitrogen until solids were in solution, followed by heating to 90 °C. A freshly prepared solution of 6 g AgN03 in 36 mL propylene glycol was added dropwise over 64 h. After quenching in an ice bath, the product was isolated by settling and centrifugation to give silver nanowires with an average diameter of 40.23 nm and average length of 30.9 μιη, based on measurement of at least 100 nanowires.
Example 2 (Comparative)
To a 500 mL reaction vessel was charged 430 mL propylene glycol and 7.2 g of polyvinylpyrrolidone (50,000 weight average molecular weight). The mixture was stirred under nitrogen until solids were in solution, followed by heating to 90 °C. To the mixture was added 0.2 mL of a solution of 6 g AgN03 in 36 mL propylene glycol, followed by 1.14 mL of a 10 wt % solution of tetrabutylammonium chloride in propylene glycol. After these additions, 35.8 mL of a solution of 6 g AgN03 in 36 mL propylene glycol was added to the mixture. This mixture was stirred at temperature for 24 hr. After quenching in an ice bath, the product was isolated by settling and centrifugation to give silver nanowires with an average diameter of 60 nm and average length of 15.7 μιη, based on measurement of at least 100 nanowires.
Example 3
The procedure of Example 1 was repeated, changing the time period for AgN03 solution addition from 64 h to 24 h. The resulting silver nanowires had an average diameter of 44.11 nm and average length of 16.7 μιη, based on measurement of at least 100 nanowires.
Example 4
The procedure of Example 1 was repeated, changing the time period for AgN03 solution addition from 64 h to 67.3 h, and changing the reaction temperature from 90 °C to 75 °C. The resulting silver nanowires had an average diameter of 57.2 nm and average length of 20.5 μιη, based on measurement of at least 100 nanowires.
Example 5
To a reaction vessel was charged 2000 mL propylene glycol and 33.5 g of polyvinylpyrrolidone (PVP, 50,000 weight average molecular weight). The mixture was stirred with nitrogen sparging until the PVP dissolved. The mixture was then heated to 91 °C. A freshly prepared solution of 28.08 g AgN03 in 168 mL propylene glycol was pumped into the reaction vessel at a rate of 0.949 mL/min for 5 min. The silver nitrate pump was then stopped for 5 min. The silver nitrate pump was then restarted at a rate of 34.6 mL/hr and was allowed to run for 30.6 hr. At the time the silver nitrate pump was restarted, 9.4 mL of a 1 wt % solution of ammonium chloride in propylene glycol was pumped into the reaction mixture at a rate of 34.6 mL/hr. The reaction mixture was held for 25 min after the silver nitrate pump was shut off. The reaction vessel was then allowed to cool to room temperature. The resulting silver nanowires had an average diameter of 43.8 nm and average length of 22.9 μιη, based on
measurement of at least 100 nanowires.
Example 6
To a reaction vessel was charged 8000 mL propylene glycol and 134.0 g of polyvinylpyrrolidone (PVP, 50,000 weight average molecular weight). The mixture was stirred with nitrogen sparging until the PVP dissolved. The mixture was then heated to 91 °C. A freshly prepared solution of 112.32 g AgN03 in 672 mL propylene glycol was pumped into the reaction vessel at a rate of 0.44 mL/min for 5 min. The silver nitrate pump was then stopped for 5 min. The silver nitrate pump was then restarted and was allowed to run for 26.7 hr. At the time the silver nitrate pump was restarted, 37.6 mL of a 1 wt % solution of
ammonium chloride in propylene glycol was pumped into the reaction mixture at a rate of 150 mL/hr. The reaction mixture was held for 66 min after the silver nitrate pump was shut off. The reaction vessel was then allowed to cool to room temperature. The resulting silver nanowires had an average diameter of 39.8 nm and average length of 17.6 μιη, based on measurement of at least 100 nanowires.
The invention has been described in detail with particular reference to a presently preferred embodiment, 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 therein.
Claims
1. A method comprising:
providing at least one first composition comprising 1,2-propylene glycol, polyvinyl pyrrolidone, and ammonium chloride;
adding at least one second composition to the at least one first composition, the adding occurring over the course of at least about 16 hrs, and the at least one second composition comprising 1,2-propylene glycol and silver nitrate; and
reducing at least a portion of the silver nitrate to silver nanowires.
2. The method according to claim 1, further comprising heating the at least one first composition to a temperature less than about 140 °C.
3. The method according to claim 1, further comprising heating the at least one first composition to a temperature between about 80 °C and about 120 °C.
4. The method according to claim 1, further comprising heating the at least one first composition to a temperature of about 90 °C.
5. The method according to claim 1, wherein the at least first composition further comprises silver nitrate.
6. The method according to claim 5, wherein providing the at least one first composition comprises:
providing at least one third composition comprising silver nitrate; and
adding at least one fourth composition to the at least one third composition, the at least one fourth composition comprising ammonium chloride.
7. The method according to claim 5, wherein providing the at first composition comprises:
providing at least one third composition comprising polyvinyl pyrrolidone;
forming at least one fourth composition by adding at least one fifth composition to the at least one third composition, the at least one fifth
composition comprising silver nitrate; and
adding at least one sixth composition to the at least one fourth composition, the at least one sixth composition comprising ammonium chloride.
8. The method according to claim 7, further comprising heating the at least one third composition to a temperature less than about 140 °C.
9. The method according to claim 7, further comprising heating the at least one third composition to a temperature between about 80 °C and about 120 °C.
10. The method according to claim 7, further comprising heating the at least one third composition to a temperature of about 90 °C.
11. The method according to claim 1, wherein the adding the at least one second composition to the at least one first composition occurs over the course of between about 20 hrs and about 28 hrs.
12. The method according to claim 1, wherein the adding the at least one second composition to the at least one first composition occurs over the course of about 24 hrs.
Applications Claiming Priority (3)
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| US201261723942P | 2012-11-08 | 2012-11-08 | |
| US14/043,966 US20140123808A1 (en) | 2012-11-08 | 2013-10-02 | Nanowire preparation methods, compositions, and articles |
| PCT/US2013/063155 WO2014074247A1 (en) | 2012-11-08 | 2013-10-03 | Method for preparing a silver nanowire |
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| EP2916981A1 true EP2916981A1 (en) | 2015-09-16 |
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| EP (1) | EP2916981A1 (en) |
| JP (1) | JP2016503457A (en) |
| KR (1) | KR20150082285A (en) |
| CN (1) | CN104768679A (en) |
| TW (1) | TW201417913A (en) |
| WO (1) | WO2014074247A1 (en) |
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| US20150287494A1 (en) | 2014-04-08 | 2015-10-08 | Carestream Health, Inc. | Nitrogen-containing compounds as additives for transparent conductive films |
| TWI695848B (en) | 2015-03-03 | 2020-06-11 | 德商巴斯夫歐洲公司 | Silver nanowire synthesis with (meth) acrylate based capping agents |
| CN104999089B (en) * | 2015-07-15 | 2017-07-25 | 济宁利特纳米技术有限责任公司 | The preparation method of nano silver wire in a kind of hydrophobic phase |
| WO2017057326A1 (en) | 2015-09-30 | 2017-04-06 | 昭和電工株式会社 | Method for producing metal nanowire |
| CN105414561B (en) * | 2015-12-28 | 2018-04-10 | 中国科学技术大学 | A kind of silver nanowire assembly and its preparation method and flexible conductor |
| CN108884347A (en) | 2016-04-06 | 2018-11-23 | 巴斯夫欧洲公司 | Process for preparing a product containing surface-modified silver nanowires and use of the product |
| CN107486561B (en) * | 2017-07-27 | 2020-09-15 | 南京邮电大学 | A method for large-scale atmospheric preparation and separation of silver nanowires |
| CN109503889B (en) * | 2018-12-17 | 2020-11-13 | 安徽大学 | Preparation method of silver nanowire hybrid filler and composite material using filler |
| CN116618643A (en) * | 2023-06-09 | 2023-08-22 | 深圳市志凌伟业技术股份有限公司 | A method for synthesizing silver nanowires based on halide-free salts |
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| CN100342064C (en) | 2005-09-23 | 2007-10-10 | 浙江大学 | Silver nanometer wire synthesizing process |
| TWI397446B (en) * | 2006-06-21 | 2013-06-01 | Cambrios Technologies Corp | Methods of controlling nanostructure formations and shapes |
| WO2009063744A1 (en) | 2007-11-16 | 2009-05-22 | Konica Minolta Holdings, Inc. | Method for producing metal nanowire, metal nanowire and transparent conductor |
| JP2009155674A (en) * | 2007-12-25 | 2009-07-16 | Osaka Univ | Method for producing metal nanoparticles |
| EP2470318A2 (en) * | 2009-08-25 | 2012-07-04 | Cambrios Technologies Corporation | Methods for controlling metal nanostructures morphology |
| KR101904912B1 (en) | 2010-01-15 | 2018-10-08 | 씨에이엠 홀딩 코포레이션 | Low-haze transparent conductor |
| US9321108B2 (en) | 2010-09-09 | 2016-04-26 | Carestream Health, Inc. | Nanowire preparation methods, compositions, and articles |
| US9017449B2 (en) * | 2010-12-09 | 2015-04-28 | Carestream Health, Inc. | Nanowire preparation methods, compositions, and articles |
| US9017450B2 (en) * | 2010-12-09 | 2015-04-28 | Carestream Health, Inc. | Nanowire preparation methods, compositions, and articles |
| US9101983B2 (en) * | 2010-12-09 | 2015-08-11 | Carestream Health, Inc. | Nanowire preparation methods, compositions, and articles |
| KR20140026331A (en) * | 2010-12-17 | 2014-03-05 | 세이코 피엠씨 가부시키가이샤 | Process for producing silver nanowires and agent for controlling growth of silver nanowires |
| CN102259190A (en) * | 2011-06-16 | 2011-11-30 | 浙江科创新材料科技有限公司 | Method for quickly preparing nano silver wires with high length-diameter ratio in large batch |
| US20130192423A1 (en) * | 2012-01-27 | 2013-08-01 | Blue Nano Inc. | Method of producing silver nanowires |
-
2013
- 2013-10-02 US US14/043,966 patent/US20140123808A1/en not_active Abandoned
- 2013-10-03 KR KR1020157011813A patent/KR20150082285A/en not_active Withdrawn
- 2013-10-03 CN CN201380057850.9A patent/CN104768679A/en active Pending
- 2013-10-03 JP JP2015541771A patent/JP2016503457A/en active Pending
- 2013-10-03 EP EP13776920.4A patent/EP2916981A1/en not_active Withdrawn
- 2013-10-03 WO PCT/US2013/063155 patent/WO2014074247A1/en not_active Ceased
- 2013-10-18 TW TW102137803A patent/TW201417913A/en unknown
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| CN104768679A (en) | 2015-07-08 |
| TW201417913A (en) | 2014-05-16 |
| JP2016503457A (en) | 2016-02-04 |
| US20140123808A1 (en) | 2014-05-08 |
| WO2014074247A1 (en) | 2014-05-15 |
| KR20150082285A (en) | 2015-07-15 |
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