Patent Application
20230241671
The present invention relates to metal powders. Particularly, the present invention relates to a metal powder suitable for purposes that require electrical conductivity.
An electrically-conductive paste is used to produce a printed circuit board of an electronic device. The paste contains a metal powder, a binder, and a solvent. The metal powder is an ensemble of fine metal particles. Processes such as printing and etching using the paste result in a pattern by which one element is coupled to another element. The pattern is heated. The heating leads to sintering of the fine metal particles adjacent to one another. The pattern is a path for electrons and thus needs to have high electrical conductivity.
Japanese Laid-Open Patent Application Publication No. 2007-254845 discloses particles made of silver and shaped as flakes. The particles are formed by processing spherical particles using a ball mill. The particles overlap one another in a pattern. This overlapping can contribute to the electrical conductivity of the pattern.
WO 2016/125355 discloses particles made of silver and shaped as flakes. The particles are obtained by precipitation from a liquid in which silver oxalate is dispersed. The particles overlap one another in a pattern. This overlapping can contribute to the electrical conductivity of the pattern.
PTL 1: Japanese Laid-Open Patent Application Publication No. 2007-254845
PTL 2: WO 2016/125355
The patterns obtained from the conventional flaky particles are unsatisfactory in the through-thickness electrical conductivity. An object of the present invention is to provide a metal powder by the use of which a pattern having high electrical conductivity can be obtained.
A fine layered metal particle according to the present invention includes:
Preferably, the second layer is partially spaced from the first layer.
Preferably, a material of the fine layered metal particle is an electrically-conductive metal. A preferred electrically-conductive metal is silver or copper.
In another aspect, a metal powder according to the present invention includes fine metal particles. The fine metal particles include fine layered metal particles. Each of the fine layered metal particles includes:
Preferably, a proportion of the fine layered metal particles in the fine metal particles is 30 mass % or more.
Preferably, an average particle diameter of the metal powder is from 0.1 to 30 μm. Preferably, a standard deviation of particle diameters of the metal powder is 15 μm or less.
In a pattern obtained from the metal powder according to the present invention, the adjacent metal particles overlap one another. This overlapping contributes to the electrical conductivity of the pattern in the length direction. In each of the metal particles, the electrical resistance between the first layer and the second layer is very low since the second layer is integral with the first layer. The metal particles contribute to the electrical conductivity of the pattern in the thickness direction. The pattern has excellent electrical conductivity.
The following will describe the present invention in detail based on preferred embodiments with appropriate reference to the drawings.
A metal powder according to the present invention is an ensemble of fine metal particles. The fine metal particles include fine layered metal particles.
The metal powder is typically used in an electrically-conductive paste. The electrically-conductive paste can be obtained by mixing the metal powder, a solvent, a binder, a dispersant, etc.
As shown in
The center layer 4 is shaped as a flake. In other words, the center layer 4 is in the shape of a thin sheet. The outline of the center layer 4 as viewed in plan is polygonal (typically triangular or hexagonal). The center layer 4 is a crystal of an electrically-conductive metal. Preferably, the center layer 4 is a crystal of silver or copper.
The upper middle layer 6 is shaped as a flake. In other words, the upper middle layer 6 is in the shape of a thin sheet. The upper middle layer 6 is a crystal of an electrically-conductive metal. Preferably, the upper middle layer 6 is a crystal of silver or copper. The upper middle layer 6 is located on the center layer 4. The upper middle layer 6 is integral with the center layer 4. The middle layer 6 belongs to the same crystal as the center layer 4. In the present invention, when two layers belong to the same crystal, these layers are considered integral. Two layers integral with each other need not belong to the same crystal grain. In other words, each of the layers may be a polycrystal. As the upper middle layer 6 is integral with the center layer 4, the electrical resistance between the center layer 4 and the upper middle layer 6 is very low.
As described later, the center layer 4 and the upper middle layer 6 are formed by crystal growth. Thus, in a real fine layered metal particle 2, the center layer 4 and the upper middle layer 6 are not clearly distinguishable. In the front view of
As is clear from
The upper end layer 8 is shaped as a flake. In other words, the upper end layer 8 is in the shape of a thin sheet. The upper end layer 8 is a crystal of an electrically-conductive metal. Preferably, the upper end layer 8 is a crystal of silver or copper. The upper end layer 8 is located on the upper middle layer 6. The upper end layer 8 is integral with the upper middle layer 6. The upper end layer 8 belongs to the same crystal as the upper middle layer 6. Thus, the electrical resistance between the upper middle layer 6 and the upper end layer 8 is very low.
As described later, the upper middle layer 6 and the upper end layer 8 are formed by crystal growth. Thus, in a fine layered metal particle 2, the upper middle layer 6 and the upper end layer 8 are not clearly distinguishable. In the front view of
As is clear from
The lower middle layer 10 is shaped as a flake. In other words, the lower middle layer 10 is in the shape of a thin sheet. The lower middle layer 10 is a crystal of an electrically-conductive metal. Preferably, the lower middle layer 10 is a crystal of silver or copper. The lower middle layer 10 is located under the center layer 4. The lower middle layer 10 is integral with the center layer 4. The lower middle layer 10 belongs to the same crystal as the center layer 4. Thus, the electrical resistance between the center layer 4 and the lower middle layer 10 is very low.
As described later, the center layer 4 and the lower middle layer 10 are formed by crystal growth. Thus, in a real fine layered metal particle 2, the center layer 4 and the lower middle layer 10 are not clearly distinguishable. In the front view of
As is clear from
The lower end layer 12 is shaped as a flake. In other words, the lower end layer 12 is in the shape of a thin sheet. The lower end layer 12 is a crystal of an electrically-conductive metal. Preferably, the lower end layer 12 is a crystal of silver or copper. The lower end layer 12 is located under the lower middle layer 10. The lower end layer 12 is integral with the lower middle layer 10. The lower end layer 12 belongs to the same crystal as the lower middle layer 10. Thus, the electrical resistance between the lower middle layer 10 and the lower end layer 12 is very low.
As described later, the lower middle layer 10 and the lower end layer 12 are formed by crystal growth. Thus, in a real fine layered metal particle 2, the lower end layer 12 and the lower middle layer 10 are not clearly distinguishable. In the front view of
As is clear from
In the fine layered metal particle 2, the center layer 4, the upper middle layer 6, the upper end layer 8, the lower middle layer 10, and the lower end layer 12 belong to the same crystal.
As shown in
For the paste, the electrical resistance in the length direction is low, and the electrical resistance in the thickness direction is also low. With the use of the fine layered metal particles 2 according to the present invention, a paste having high electrical conductivity can be obtained.
As previously stated, each of the fine layered metal particles 2 has spaces (S1 to S4) between the layers. The apparent density of the metal powder containing the fine layered metal particles 2 each of which has such spaces is low. As previously stated, each of the layers is integral with the other layers. Thus, the electrical resistance between the layers is low despite the presence of the spaces. The metal powder is light-weight and has low electrical resistance. A paste containing the metal powder can be obtained at low cost.
The fine layered metal particle 2 as shown in
The fine layered metal particle 2 as shown in
The metal powder may contain fine metal particles other than the fine layered metal particles 2. Examples of the fine metal particles other than the fine layered metal particles 2 include block-shaped particles, spherical particles, flaky particles, and polyhedral particles.
In view of the electrical conductivity, the proportion of the fine layered metal particles 2 in the fine metal particles is preferably 30 mass % or more, more preferably 50 mass % or more, and particularly preferably 60 mass % or more. The proportion is ideally 100 mass %.
The average particle diameter D50 of the metal powder is preferably from 0.1 to 30 μm. The use of the metal powder having an average particle diameter D50 of 0.1 μm or more can achieve a high filling ratio in printing. From this viewpoint, the average particle diameter D50 is more preferably 2.0 μm or more and particularly preferably 3.0 μm or more. The use of the metal powder having an average particle diameter D50 of 30 μm or less can result in a fine pattern 14. From this viewpoint, the average particle diameter D50 is more preferably 15 μm or less and particularly preferably 7μm or less.
In view of the filling ratio, the minimum particle diameter Dmin is preferably 0.1 μm or more. In view of the fineness of the pattern 14, the maximum particle diameter D50max is preferably 30 μm or less.
The standard deviation σ of the particle diameters of the metal powder is preferably 15 μm or less. The use of the metal powder having a standard deviation σ of 15 μm or less can result in a homogeneous pattern 14. From this viewpoint, the standard deviation σ is more preferably 10 μm or less and particularly preferably 7 μm or less.
The average particle diameter D50, the minimum particle diameter Dmin, the maximum particle diameter D50max, and the standard deviation σ are measured by a laser diffraction particle size distribution analyzer. An example of the analyzer is “LA-950 V2” of HORIBA, Ltd.
Preferably, the metallographic structure of the fine layered metal particle 2 is monocrystalline. Such fine layered metal particles 2 can contribute to the electrical conductivity of a paste.
The fine layered metal particle 2 may include a metal and an organic compound attached to a surface of the metal. The organic compound is chemically bonded to the metal. The main component of the fine layered metal particle 2 is a metal. The proportion of the metal in the fine layered metal particle 2 is preferably 99.0 mass % or more and particularly preferably 99.5 mass % or more. The fine layered metal particle 2 may be free of any organic compound.
The following describes an example of the method of producing the metal powder. In the production method, a silver powder is obtained through a reduction process. The production method includes the steps of:
In the present invention, the flakes grow generally in the thickness direction (the upward/downward direction in
The silver salt in the aqueous solution prepared in the step (1) is preferably silver nitrate. The concentration of the silver salt in the aqueous solution is preferably from 0.1 to 1.0 M. The use of the aqueous solution having a concentration of 0.1 M or more can accelerate the growth of the particles. From this viewpoint, the concentration is more preferably 0.3 M or more and particularly preferably 0.4 M or more. The use of the aqueous solution having a concentration of 1.0 M or less increases the likelihood of precipitation of flaky layers. From this viewpoint, the concentration is more preferably 0.8 M or less and particularly preferably 0.7 M or less.
As the aqueous solution prepared in the step (1) contains an acid, the pH of the aqueous solution can be adjusted. In order to prevent aggregation of the particles during the crystal growth and thus increase the likelihood of precipitation of flaky layers, the pH is preferably 5 or less, more preferably 3 or less, and particularly preferably 2 or less. Examples of acids suitable for the pH adjustment include acetic acid, propionic acid, trifluoroacetic acid, hydrofluoric acid, nitric acid, hydrochloric acid, sulfuric acid, and phosphoric acid. Particularly preferred are hydrochloric acid, nitric acid, and sulfuric acid.
The aqueous solution prepared in the step (1) preferably contains a dispersant. A preferred dispersant is a glycol dispersant. The use of the aqueous solution containing a glycol dispersant can result in a silver powder in which the standard deviation σ of the particle diameters is small. A particularly preferred dispersant is polyethylene glycol.
Examples of the reductant added in the steps (2) and (3) include hydrazine, hydrazine compounds, formaldehyde, glucose, L-ascorbic acid, and D-erythorbic acid.
The rate of addition of the reductant has an impact on the formation of the fine layered metal particles 2. An extremely low rate of addition decreases the likelihood of precipitation of flak layers. An extremely high rate of addition decreases the likelihood of helical growth of the flakes. The rate is preferably such that the reductant is added in an amount necessary for reduction of 5 to 30 g of silver nitrate per second. The rate is particularly preferably such that the reductant is added in an amount necessary for reduction of 8 to 20 g of silver nitrate per second.
In the steps (2) and (3), the stirring speed is preferably from 100 to 500 rpm. In the steps (2) and (3), the temperature of the aqueous solution is preferably from 20 to 80° C. The time spent in the steps (2) and (3) (i.e., stirring time) is preferably from 10 to 60 minutes.
Means for obtaining the fine layered metal particles 2 includes:
The following will show the effects of the present invention by means of examples. The present invention should not be construed in a limited manner on the basis of the description of the examples.
Twenty cc of hydrazine was added to 0.5 liters of distilled water to obtain a reductant liquid. Fifty g of silver nitrate was added to 1 liter of distilled water, and 5 g of polyethylene glycol was further added to obtain an aqueous solution. Sulfuric acid was added to the aqueous solution until the pH of the aqueous solution reached 2. The reductant liquid was added to the aqueous solution at a rate of 100 cc/sec while the aqueous solution was stirred at a speed of 150 rpm. The stirring was further continued for 30 minutes while the temperature of the aqueous solution was maintained at 20° C. A silver powder containing fine layered metal particles was precipitated from the aqueous solution.
A silver powder of Example 2 was obtained in the same manner as in Example 1, except that 10 g of polyethylene glycol was added. A silver powder of Example 3 was obtained in the same manner as in Example 1, except that 20 g of polyethylene glycol was added.
A silver powder containing fine flaky particles was obtained through a reaction in an autoclave. This silver powder production method is approximately the same as the production method as disclosed in WO 2016/125355.
A silver powder of Comparative Example 2 was obtained in the same manner as in Example 1, except that the concentration of silver nitrate in the aqueous solution was 0.1 M, polyvinylpyrrolidone was used instead of polyethylene glycol, and the stirring speed was 300 rpm. The fine particles of the silver powder were spherical.
A silver powder obtained by the method of Comparative Example 2 was processed by a bead mill to form the particles into flakes. Thus, a silver powder of Comparative Example 3 was obtained.
Each of the silver powders was dispersed in methanol to obtain a paste. The silver concentration in the paste was 70 mass %. A glass slide was subjected to masking to make a surface to be coated with the paste. The surface had a size of 8 mm×50 mm The paste was applied to the surface. The paste was held at 150° C. for 30 minutes to obtain a sintered material. The thickness of the sintered material was 10 μm. The specific electrical resistance of the sintered material was measured using a measurement device of Advanced Instrument Technology (Contact 4-Point Probe). The results are shown in Table 1 below.
The specific electrical resistance was measured in the same manner as in Evaluation 1, except that the sintering temperature was 130° C. The results are shown in Table 1 below.
As seen from table 1, the sintered materials obtained from the silver powders of Examples had high electrical conductivity. The evaluation results demonstrate the superiority of the present invention.
The metal powder according to the present invention can be used in various pastes such as a paste for a printed circuit board, a paste for an electromagnetic shielding film, a paste for an electrically-conductive adhesive, and a paste for die bonding.
2 fine layered metal particle
4 center layer
6 upper middle layer
8 upper end layer
10 lower middle layer
12 lower end layer
14 pattern
16 base
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-173712 | Oct 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/028883 | 8/4/2021 | WO |
