Wafer level packaging is the technology of packaging integrated circuits fabricated on a wafer without slicing a wafer into individual circuits (dice). The wafer is typically composed of semiconductor material such as crystallized Silicon. Wafer level packaging is in contrast to the more conventional method of slicing a wafer into individual circuits (dice) and then packaging each die individually.
When performing wafer level packaging, dielectric material is often used to separate and insulate metal layers from circuitry formed on substrates and to separate and insulate metal layers from other metal layers. As disclosed further herein as a substitute for use of traditional dielectric material, one or more layers of catalytic adhesive can be used to reduce processing steps necessary for wafer level packaging. A catalytic adhesive is dielectric material that will adhere to a wafer surface and that includes catalytic particles that will reduce electroless copper (Cu) from Cu++ to Cu.
For example, wafer level packaging includes a first layer of a catalytic adhesive on a wafer surface. The catalytic adhesive includes catalytic particles that will reduce electroless copper (Cu) from Cu++ to Cu. Metal traces are formed in trace channels within the first layer of catalytic adhesive. The trace channels extend below a surface of the first layer of the catalytic material. The metals traces are also in contact with integrated circuit pads on the surface of the wafer.
For example, the metal traces are formed using a metal plating process that includes an electroless copper bath. For example, the catalytic particles are composed of at least one of: palladium (Pd) particles, iron (Fe) particles, and silver (Ag) particles.
For example, the trace channels are formed using laser ablation. Alternatively, the trace channels are formed by applying resist over the first layer of catalytic adhesive, exposing and developing the resist to delineate locations of the trace channels, and performing plasma etching to form the trace channels. Alternatively, the trace channels are formed by applying foil over the first layer of catalytic adhesive, applying resist over the foil, exposing and developing the resist to expose portions of the foil that delineate locations of the trace channels, etching the exposed portions of the foil, and performing plasma etching to form the trace channels.
Additionally, the first layer of catalytic adhesive may be coated with non-catalytic material before forming trace channels in the catalytic adhesive.
For example, a second layer of the catalytic adhesive may be applied over the first layer of the catalytic adhesive and over the metal traces. Trace channels can be formed in the second layer of catalytic adhesive. A metal plating process can be used to form metal traces within the trace channels formed in the second layer of catalytic adhesive.
In a block 31, a catalytic layer of adhesive is applied to a wafer surface. This is illustrated by
In
For example, catalytic adhesive 12 is a dielectric adhesive such as an epoxy, polyimide, cyanate ester or another suitable dielectric adhesive. The dielectric adhesive includes, for example, both non-catalytic and catalytic filler particles. The catalytic filler particles are composed of, for example, a metal such as palladium (Pd), iron (Fe), silver (Ag) and/or other catalytic particles used for copper plating where electroless copper (Cu) is reduced from its Cu++ to Cu. For example, the catalytic particles can be made of inorganic filler with metal coated over the inorganic filler. For example, the inorganic filler can be silicon dioxide, kaolin, or some other inorganic filler with suitable properties for the particular application.
In one implementation, palladium powder that includes palladium catalytic particles is made out of inorganic fillers primarily Kaolin. For example, the inorganic fillers are produced by contacting a salt palladium, at the surface of a filler such as aluminum silicate, and clays such as Kaolin with a reducing agent. Alternatively, instead of salt of palladium, salt of another metal such as silver can be used.
Hydrazine hydrate can be used as a reducing agent to reduce the palladium salt to palladium metal. The filler can be added into a mixing tank with water in a form of slurry and then a palladium chlorine (PdCl) and hydrochloric acid (HCl) solution added into the mixture followed by the hydrazine hydrate. For more information on making such a catalytic power, see U.S. Pat. No. 4,287,253.
Thickness of catalytic adhesive 12 is dependent on application. For example, catalytic adhesive 12 is 10 microns thick or greater. Alternatively, catalytic adhesive 12 is less than 10 microns thick.
Optionally, a coating of non-catalytic material is placed over catalytic adhesive 12. For example, the non-catalytic material is composed of a thin non-catalytic adhesive or dielectric layer applied over catalytic adhesive 12. This coating can be applied, for example, using spin coating or other conventional or non-conventional processes. The thickness of the resulting non-catalytic material is, for example, in the range of approximately 0.25-1.5 mils. After application the coating can be cured thermally or can be cured using a UV process.
In a block 34, IC pads 11 are exposed and trace channels are formed. For example, laser ablation is used to break the surface of non-catalytic material and catalytic adhesive 12 to expose IC pads 11 and to form trace channels, as illustrated by
As an alternative to using laser ablation to form channels and expose IC pads 11, resist can be applied. For example, the resist is exposed and developed to delineate locations of the trace channels and the IC pads. For example, resist thickness is thicker than the depth of the trace channels. For example, for a channel depth of 0.5 mils, resist thickness can be 1.0 to 1.5 mils. The formation of the trace channels can then be performed using plasma etching with a combination of gasses (e.g., O2, CF4, Ar, etc.) along with the proper power and duration. It is expected the channel will be etched at a different rate than the resist. For example, the resist thickness should be sufficiently thicker that the channel depth so that when the channel depth is reached there is some resist left protecting unexposed regions of the surfaces of non-catalytic material. After plasma etching, the remaining resist can be removed by a resist stripper. If needed, a separate or an additional deposit of resist and subsequent etch can be use to expose IC pads 11.
Alternatively, instead of protecting the surface with resist when performing plasma etch, other protective material can be used. For example, the protection can be accomplished using a foil, such as a copper foil or aluminum foil. The shiny side of the foil can be placed facing wafer 10 so the foil can be peeled off after channel formation. For example, after applying the foil, resist is applied over the foil. The resist is exposed/develop to expose the foil over the channel regions and/or over IC pads 11. The foil is etched to expose the channel regions and/or IC pads 11. The remaining resist is then stripped and the trace channels are plasma etched. Plasma etching can also be used to expose IC pads 11. The remaining foil is peeled off and processing continues.
Alternatively, channels can be formed using high pressure water cutting. The high pressure water cutting can be performed using programmable high pressure water cutting machines such as those used for cutting hard materials such as steel and stainless steel. Another mechanical processes such as drilling and routing can be used for making the trace channels.
A cleaning may be performed as necessary to remove debris from the trace channels. For example, a plasma clean can be used. Alternatively or in addition, the cleaning can be accomplished by an ultrasonic rinse using acoustic wave with a frequency within the range of 40 to 160 megahertz (MHz).
In a block 33, shown in
If necessary, the surface can be planarized, for example, using fine grid sandpaper (e.g., 420 grit to 1200 grit), lapping, fine grinding or other planarization methods. The planarization removes any excess copper that extends above the trace channels.
When it is desirable to have one or more additional layers of traces, the process can be repeated. This is illustrated for example, by block 34 where another layer of catalytic adhesive is applied to the exposed surface, and so on, as discussed above. In a block 35, the pads are exposed and channels are formed, as further discussed above. As illustrated by block 36, this can be repeated as desired.
In a block 37 a dielectric layer is deposited. The dielectric layer functions as a solder mask. It protects the traces during further processing. For example, pads formed in the trace layers or below may be exposed using process involving lasers, ultraviolet light, etc, as is known in the art. The pads are then used as interconnect areas, for example, where solder balls, copper posts or other interconnect techniques are used to connect the wafer level packaged circuit to other circuits, such as circuits mounted on a printed circuit board (PCB).
The foregoing discussion discloses and describes merely exemplary methods and embodiments. As will be understood by those familiar with the art, the disclosed subject matter may be embodied in other specific forms without departing from the spirit or characteristics thereof. Accordingly, the present disclosure is intended to be illustrative, but not limiting, of the scope of the invention, which is set forth in the following claims.
Number | Name | Date | Kind |
---|---|---|---|
3322881 | Schneble et al. | May 1967 | A |
4287253 | Leech | Sep 1981 | A |
4954185 | Kohm | Sep 1990 | A |
5112726 | Cohen et al. | May 1992 | A |
5162144 | Brown et al. | Nov 1992 | A |
5309632 | Takahashi et al. | May 1994 | A |
5419954 | Lane | May 1995 | A |
7067454 | Raybould | Jun 2006 | B2 |
7169691 | Doan | Jan 2007 | B2 |
7319050 | Chang et al. | Jan 2008 | B2 |
7334326 | Huemoeller et al. | Feb 2008 | B1 |
7632753 | Rusli et al. | Dec 2009 | B1 |
7752752 | Rusli et al. | Jul 2010 | B1 |
8779576 | Park et al. | Jul 2014 | B2 |
8836144 | Liao | Sep 2014 | B2 |
8922014 | Hu et al. | Dec 2014 | B2 |
8941222 | Hunt | Jan 2015 | B2 |
9000558 | Sarfaraz et al. | Apr 2015 | B2 |
9000587 | Kelkar et al. | Apr 2015 | B1 |
9087732 | Xu et al. | Jul 2015 | B1 |
9117714 | Weng et al. | Aug 2015 | B2 |
9136196 | Rathburn | Sep 2015 | B2 |
9922951 | Bahl | Mar 2018 | B1 |
20020195716 | Magnusen et al. | Dec 2002 | A1 |
20060055021 | Yamamoto | Mar 2006 | A1 |
20060057341 | Kawabata et al. | Mar 2006 | A1 |
20060068173 | Kajiyama et al. | Mar 2006 | A1 |
20070014975 | Ota | Jan 2007 | A1 |
20090120660 | Park et al. | May 2009 | A1 |
20100266752 | Tseng et al. | Oct 2010 | A1 |
20110048783 | Yu | Mar 2011 | A1 |
20120074094 | Chiang et al. | Mar 2012 | A1 |
Number | Date | Country |
---|---|---|
2120525 | Sep 2009 | EP |
2420593 | Feb 2012 | EP |
1208337 | Oct 1970 | GB |
WO 2009006010 | Jan 2009 | WO |
WO 2012127205 | Sep 2012 | WO |
WO2014041057 | Mar 2014 | WO |
Entry |
---|
PCT International Preliminary Report on Patentability for PCT Application PCT/US2015/014619, dated Dec. 1, 2016. |
PCT International Preliminary Report on Patentability for PCT Application PCT/US2015/014599, dated Nov. 22, 2016. |
Number | Date | Country | |
---|---|---|---|
20160148893 A1 | May 2016 | US |
Number | Date | Country | |
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Parent | 14297516 | Jun 2014 | US |
Child | 15009386 | US | |
Parent | 14281631 | May 2014 | US |
Child | 14297516 | US |