Patent Application
20230201975
This application claims priority of Taiwan Patent Application No. 110149025, filed on Dec. 28, 2021, the entirety of which is incorporated by reference herein.
The present disclosure relates to a solder ball with a concave-convex structure.
The display technology of micro-LED is a miniaturized LED array structure with self-luminous display characteristics, and each pixel can be driven independently, with high brightness, high contrast, low power consumption, high resolution and high color saturation.
At present, Micro-LEDs generally include epitaxy, mass transfer and repair technologies, among which mass-transfer technology is a key to whether micro-LED products can be commercialized, and the steps include transfer and die bonding. On the market, products by companies such as LuxVue use electrostatic force to adsorb tiny dies and have transfer heads that have a bipolar structure that can apply positive voltage and negative voltage to respectively grab and release the dies. X-Celeprint uses an elastomer imprint head to control the speed of the interface bonding to grab and release the die, and then transfer it to the substrate. There are two kinds of die-bonding materials, one is solder, and the other is anisotropic conductive film (ACF). Compared with solder, existing anisotropic conductive film can still conduct the circuit, but it needs to be pressed during the mass transfer, which makes it easy for the chip electrode to crack. On the other hand, the solder-based die-bonding material can be bonded directly onto the chip electrode after the tin is melted to avoid problems with electrode cracking. However, due to the problems with alignment accuracy in printing in the existing process, vacuum sputtering and evaporation is most commonly used to manufacture the die-bonding material, and it is relatively expensive, with a slow processing speed, and therefore does not meet the requirements for mass production.
In accordance with one embodiment of the present disclosure, a solder ball with a concave-convex structure is provided. The solder ball with a concave-convex structure includes a tin-bismuth alloy which includes a plurality of concave portions and convex portions on its surface, wherein the height difference between the concave portions and the convex portions is between 10 nm and 200 nm, and the proportion of tin in the tin-bismuth alloy is between 28% and 52%.
In accordance with one embodiment of the present disclosure, a method for preparing a solder ball with a concave-convex structure is provided. The preparation method includes providing an acidic etching solution, wherein the acidic etching solution includes an acid and a modifier; placing a solder ball in the acidic etching solution to perform an acidic etching step; and cleaning the solder ball subjected to the acidic etching step several times with a solution containing an antioxidant protective agent to prepare the disclosed solder ball with a concave-convex structure.
In accordance with one embodiment of the present disclosure, a solder paste is provided. The solder paste includes a colloidal composition including rosin, oleic acid, epoxy resin and organic polyacid; and the disclosed solder ball with a concave-convex structure mixed in the colloidal composition.
A detailed description is given in the following embodiments with reference to the accompanying drawings.
In the present disclosure, the self-assembled solder paste including the solder balls with the concave-convex structure is patterned by a steel-plate printing process. After reflow, it is assembled to the electrode, and then the micro light-emitting diode is joined thereon. As the size of the solder balls decreases, its surface area increases and the concentration of the oxide layer increases, which affects the reflowability and the connection characteristics between the electrodes. In the present disclosure, through surface modification, the solder balls can be self-aggregated on the electrodes after reflow, which can speed up the process speed, solve the reflowability, and improve the connection with the electrodes, so that the micro-LED display can be mass-produced. In addition, the disclosed self-assembled solder paste with low-temperature (160° C.) reflow characteristics can also solve the problem that the imprint head of the mass transfer head fails due to high temperature reflow (260° C.).
Referring to
As shown in
In some embodiments, the particle size of the solder ball 10 with concave-convex structure is between about 0.5 μm and about 12 μm.
In accordance with one embodiment of the present disclosure, a solder paste is provided. The solder paste includes colloidal composition and solder balls mixed in the colloidal composition. The colloidal composition includes rosin, oleic acid, epoxy resins such as 1,2-cyclohexanedicarboxylate diglycidyl ester, and organic polyacids. The mixed solder ball is shown in
In some embodiments, in the colloidal composition, the ratio among rosin, oleic acid, 1,2-cyclohexanedicarboxylate diglycidyl ester and organic polyacid is about 30-50: 5-20:5-20: 30-50.
In some embodiments, the organic polyacid includes glutaric acid.
In accordance with one embodiment of the present disclosure, a method for preparing a solder ball with a concave-convex structure is provided, including the following steps. First, an acidic etching solution is provided. Next, a solder ball is placed in the acidic etching solution to perform an acidic etching step. Next, the solder ball subjected to the acidic etching step is cleaned with a solution containing an antioxidant protective agent several times to prepare a solder ball with a concave-convex structure. The acidic etching solution includes an acid and a modifier. The prepared solder ball with a concave-convex structure is shown in
In some embodiments, the acid in the acidic etching solution includes inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, oxalic acid or carboxylic acid. In some embodiments, the acid in the acidic etching solution includes organic acids such as glutaric acid, hexanedioic acid or oleic acid.
In some embodiments, the viscosity of the acidic etching solution is between about 30 cps and about 3000 cps.
In some embodiments, the modifier in the acidic etching solution includes polyols or ionic polymers. In some embodiments, the polyol includes ethylene glycol, glycerol or propylene glycol. In some embodiments, the ionic polymer includes anionic polyacrylamide, acid salt of styrene-maleimide copolymer or ammonium salt of styrene-maleic anhydride copolymer.
In some embodiments, the period of the acidic etching step is between about 5 minutes and about 4 hours.
In some embodiments, the antioxidant protective agent includes rosin, rosin derivatives, fatty acid, titanium complex, zirconium complex or long-carbon-chain thiol.
The effect of the light-color conversion layer of the embodiment of the present disclosure will be described below with experimental examples and comparative examples.
First, the brands and models of materials and testing instruments used in the following preparation examples and examples will be described.
T7-type solder ball: manufacturer: 5N plus; particle size distribution: between 2 μm and 11 μm.
T10-type solder ball: manufacturer: 5N plus; particle size distribution: between 1 μm and 4 μm.
Scanning electron microscope (SEM): FE-SEM JEOL JSM-6500F.
Focused ion beam (FIB): Thermal Fisher G4.
Transmission electron microscope (TEM): JEOL JEM-2100F.
Preparation of solder ball (I) with concave-convex structure (T7-type solder ball; in 1N hydrochloric acid solution for 5 minutes)
2 g of T7-type solder balls were placed in a 1N hydrochloric acid solution (viscosity: 35.5 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 5 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (I).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 1.
Preparation of solder ball (II) with concave-convex structure (T7-type solder ball; in 1N hydrochloric acid solution for 30 minutes)
2 g of T7-type solder balls were placed in a 1N hydrochloric acid solution (viscosity: 35.5 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 30 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (II).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 1.
Preparation of solder ball (III) with concave-convex structure (T7-type solder ball; in 1N hydrochloric acid solution for 30 minutes)
2 g of T7-type solder balls were placed in a 1N hydrochloric acid solution (viscosity: 2156 cps) containing 40% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 30 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (III).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 1.
Preparation of solder ball (IV) with concave-convex structure (T7-type solder ball; in 1N hydrochloric acid solution for 30 minutes)
2 g of T7-type solder balls were placed in a 1N hydrochloric acid/glycerol solution (viscosity: 316.5 cps), mixed and stirred for 30 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (IV).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 1.
Preparation of solder ball (V) with concave-convex structure (T7-type solder ball; in 1N hydrochloric acid solution for 2 hours)
2 g of T7-type solder balls were placed in a 1N hydrochloric acid solution (viscosity: 35.5 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 2 hours to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (V).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 1.
Preparation of solder ball (VI) with concave-convex structure (T7-type solder ball; in 2N hydrochloric acid solution for 5 minutes)
2 g of T7-type solder balls were placed in a 2N hydrochloric acid solution (viscosity: 37.8 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 5 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (VI).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio (the average value of measurement in three areas was taken) of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 1.
Preparation of solder ball (VII) with concave-convex structure (T7-type solder ball; in 2N hydrochloric acid solution for 30 minutes)
2 g of T7-type solder balls were placed in a 2N hydrochloric acid solution (viscosity: 37.8 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 30 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (VII).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. In this preparation example, a solder ball (VII) was taken and measured by TEM. The particle size thereof was 7 μm, and the surface appearance thereof is shown in
Preparation of solder ball (VIII) with concave-convex structure (T7-type solder ball; in 2N hydrochloric acid solution for 2 hours)
2 g of T7-type solder balls were placed in a 2N hydrochloric acid solution (viscosity: 37.8 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 2 hours to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (VIII).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 1.
Preparation of solder ball (IX) with concave-convex structure (T10-type solder ball; in 1N hydrochloric acid solution for 5 minutes)
2 g of T10-type solder balls were placed in a 1N hydrochloric acid solution (viscosity: 35.5 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 5 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (IX).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 2.
Preparation of solder ball (X) with concave-convex structure (T10-type solder ball; in 1N hydrochloric acid solution for 30 minutes)
2 g of T10-type solder balls were placed in a 1N hydrochloric acid solution (viscosity: 35.5 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 30 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (X).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 2.
Preparation of solder ball (XI) with concave-convex structure (T10-type solder ball; in 1N hydrochloric acid solution for 30 minutes)
2 g of T10-type solder balls were placed in a 1N hydrochloric acid solution (viscosity: 2156 cps) containing 40% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 30 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (XI).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 2.
Preparation of solder ball (XII) with concave-convex structure (T10-type solder ball; in 1N hydrochloric acid solution for 30 minutes)
2 g of T10-type solder balls were placed in a IN hydrochloric acid/glycerol solution (viscosity: 316.5 cps), mixed and stirred for 30 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (XII).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 2.
Preparation of solder ball (XIII) with concave-convex structure (T10-type solder ball; in 1N hydrochloric acid solution for 2 hours)
2 g of T10-type solder balls were placed in a iN hydrochloric acid solution (viscosity: 35.5 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 2 hours to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (XIII).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 2.
Preparation of solder ball (XIV) with concave-convex structure (T10-type solder ball; in 2N hydrochloric acid solution for 5 minutes)
2 g of T10-type solder balls were placed in a 2N hydrochloric acid solution (viscosity: 37.8 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 5 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (XIV).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 2.
Preparation of solder ball (XV) with concave-convex structure (T10-type solder ball; in 2N hydrochloric acid solution for 30 minutes)
2 g of T10-type solder balls were placed in a 2N hydrochloric acid solution (viscosity: 37.8 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 30 minutes to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (XV).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. In this preparation example, a solder ball (XV) was taken and measured by TEM. The particle size thereof was 1 and the surface appearance thereof is shown in
Preparation of solder ball (XVI) with concave-convex structure (T10-type solder ball; in 2N hydrochloric acid solution for 2 hours)
2 g of T10-type solder balls were placed in a 2N hydrochloric acid solution (viscosity: 37.8 cps) containing 30% acid salt (modifier) of styrene-maleimide copolymer (SMA1000I), mixed and stirred for 2 hours to perform an acidic etching step. Next, the solder balls were centrifuged to remove liquid. Next, the solder balls were washed with an ethanol solution containing 30 wt % rosin after aeration several times to obtain the modified solder balls (XVI).
The elemental analysis of the modified solder ball was performed by SEM to obtain the composition ratio of tin in the tin-bismuth alloy, and sliced by FIB. The height of the concave structure and convex structure on the surface of the solder ball was measured by TEM. The composition ratio of tin and the height difference between the concave and convex are shown in Table 2.
Unmodified T7-type solder balls were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and it was observed whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C. The results are shown in Table 1.
The modified solder balls (I) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 1.
The modified solder balls (II) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 1.
The modified solder balls (III) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 1.
The modified solder balls (IV) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 1.
The modified solder balls (V) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 1.
The modified solder balls (VI) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 1.
The modified solder balls (VII) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 1.
The modified solder balls (VIII) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 80%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 1.
Unmodified T10-type solder balls were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and it was observed whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C. The results are shown in Table 2.
The modified solder balls (IX) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 2.
The modified solder balls (X) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 2.
The modified solder balls (XI) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 2.
The modified solder balls (XII) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 2.
The modified solder balls (XIII) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 2.
The modified solder balls (XIV) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 2.
The modified solder balls (XV) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 2.
The modified solder balls (XVI) were added to a flux to form a solder paste. The flux was formulated with the ratio of rosin/oleic acid/1,2-cyclohexanedicarboxylate diglycidyl ester/glutaric acid (4/1/1/4). The solid content of the solder paste was 60%. After that, the solder paste was printed on the electrodes by steel-plate printing, and the reflow effect was observed (it was observed that whether the solder balls could be melted and connected to the electrodes after reflow at a reflow temperature of 160° C.). The results are shown in Table 2.
According to Table 1 and Table 2, it can be seen from the test results that when the acidic etching period of the disclosed solder balls is 5 minutes (such as Examples 1, 3, 5 and 7) and 30 minutes (such as Examples 2, 4, 6 and 8), the acidic etching depth can be controlled, so that the height difference between the concave and convex is between 10 nm and 200 nm, and the composition ratio of tin in the tin-bismuth alloy is between 28% and 52%. In this way, after the solder balls are prepared into the solder paste, the solder paste can be effectively connected to the electrodes during the reflow. On the contrary, the solder paste made of unmodified solder balls (such as Comparative Examples 1 and 4) cannot be effectively reflowed at a temperature of 160° C., and then cannot be effectively attached to the electrodes. When the size of the solder balls is selected T7 type (for example, the particle size is between 2 μm and 11 μm) and T10 type (for example, the particle size is between 1 μm and 4 μm), using strong acid and the acidic etching period exceeding two hours may cause the solder balls to be over-etched or even to crack. The solder paste cannot be effectively reflowed at 160° C. and attached on the electrodes.
The self-assembled solder paste is patterned by a steel-plate printing process. After reflow, it is assembled to the electrode, and then the micro light-emitting diode is joined thereon. As the size of the existing micro light-emitting diodes is reduced to the wafer size of 30*15 μm2, the size of the electrodes is also reduced to 15*10 μm2, and the spacing between the electrodes is reduced to 10 μm. The solder balls with a size between 0.5 μm and 12 μm are selected. Through surface modification, the concentration of the oxide layer on the surface of the solder ball is reduced, resulting in concave and convex structures. The solder balls can thus be self-aggregated on the electrodes after reflow, which can speed up the process speed, solve the reflowability, and improve the connection with the electrodes, so that the micro-LED display can be mass-produced. In addition, the disclosed self-assembled solder paste with low-temperature (160° C.) reflow characteristics can also solve the problem that the imprint head of the mass transfer head fails due to high temperature reflow (260° C.).
While the invention has been described by way of example and in terms of the preferred embodiments, it should be understood that the invention is not limited to the disclosed embodiments. On the contrary, it is intended to cover various modifications and similar arrangements (as would be apparent to those skilled in the art). Therefore, the scope of the appended claims should be accorded the broadest interpretation so as to encompass all such modifications and similar arrangements.
| Number | Date | Country | Kind |
|---|---|---|---|
| 110149025 | Dec 2021 | TW | national |
