Conductive pastes containing silver carboxylates
US-9283618-B2 · Mar 15, 2016 · US
US9902862B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9902862-B2 |
| Application number | US-201615203029-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 6, 2016 |
| Priority date | Jul 6, 2016 |
| Publication date | Feb 27, 2018 |
| Grant date | Feb 27, 2018 |
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A method is provided to make a nano-silver paste. An organic acid is used as a protective agent. Silver nitrate is used as a source of silver ions to reduce silver nanoparticles on a surface protected by the organic acid. The particle size of the silver nanoparticle is 45 nanometers. In the other hand, a silver precursor of organic metal is synthesized. The organic metal is cracked at 200 celsius degrees (° C.) to fill pores left during sintering. After mixing the silver nanoparticle, the silver precursor and the solvent, the nano-silver paste is obtained. After being heated at 250° C. for 30 minutes, the nano-silver paste has a resistance of (3.09±0.61)×10 −5 Ω·cm. By being heated at 250° C. and applied with a pressure of 10 MPa to be hot-pressed for 30 minutes for joining copper to copper, the nano-silver paste obtains a bonding strength reaching 36 MPa.
Opening claim text (preview).
What is claimed is: 1. A method of fabricating a nano-silver paste, comprising steps of: (a) fabricating silver nanoparticles using silver nitrate as a silver ion source to produce said silver nanoparticles through a chemical reduction and using a protective agent to protect a surface of said silver nanoparticles; (b) dissolving 2-ethylhexanoic acid in methyl alcohol and adding a solution of sodium hydroxide to obtain a mixed solution and adding a solution of silver nitrate to said mixed solution to obtain a silver precursor of organic metal; and (c) mixing said silver nanoparticles, said silver precursor and a solvent to obtain a nano-silver paste, wherein said paste composition consists of a silver nanoparticle component having a particle size of 45 nm±20%. 2. The method according to claim 1 , wherein said protective agent is heptanoic acid. 3. The method according to claim 1 , wherein said protective agent has a weight occupying 6.4 percents (%)±20% of a weight of a whole there-containing said silver nanoparticles. 4. The method according to claim 1 , wherein said silver precursor is silver 2-ethylhexanoate. 5. The method according to claim 1 , wherein said solvent is selected from the group consisting of dimethylacetamide (DMAc), heptanol and α-terpineol. 6. The method according to claim 1 , wherein said silver nanoparticles, said silver precursor and said solvent are mixed at a ratio of 3:1:1.73. 7. The method according to claim 1 , further comprising hot-pressing the nano-silver paste at a temperature of 200˜250° C., such that said silver precursor in said nano-silver paste is cracked and reduces to fill pores left during sintering.
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