Semiconductor packages include one or more semiconductor chips having connections that are protectively enclosed in an encapsulation material and/or mold compound. Semiconductor packages are commonly employed in a wide range of electronic devices, such as mobile devices, and in a wide variety of applications, including telecommunication and automotive applications.
Power semiconductor packages have conductive strips for guiding signals from the chip(s) to contacts outside the package. The conductive strips are provided with metal that is deposited over or onto dielectric portions of the chip(s). The dielectric portions of the chip(s) are seeded with metal or compounds that are receptive to the metal deposition of the conductive strips. Additive processes such as ink jet printing or photolithography, for example, are subsequently employed to process the seeded dielectric portions into metal conductive strips. The seeding and the additive processes can present challenges to the package fabrication process and add expense to the finished semiconductor device.
For these and other reasons there is a need for the present invention.
One embodiment provides a method of manufacturing a semiconductor device. The method includes providing a chip on a carrier, and applying an electrically conducting layer to the chip and the carrier. The method additionally includes converting the electrically conducting layer into an electrically insulating layer.
The accompanying drawings are included to provide a further understanding of embodiments and are incorporated in and constitute a part of this specification. The drawings illustrate embodiments and together with the description serve to explain principles of embodiments. Other embodiments and many of the intended advantages of embodiments will be readily appreciated as they become better understood by reference to the following detailed description. The elements of the drawings are not necessarily to scale relative to each other. Like reference numerals designate corresponding similar parts.
In the following Detailed Description, reference is made to the accompanying drawings, which form a part hereof, and in which is shown by way of illustration specific embodiments in which the invention may be practiced. In this regard, directional terminology, such as “top,” “bottom,” “front,” “back,” “leading,” “trailing,” etc., is used with reference to the orientation of the Figure(s) being described. Because components of embodiments can be positioned in a number of different orientations, the directional terminology is used for purposes of illustration and is in no way limiting. It is to be understood that other embodiments may be utilized and structural or logical changes may be made without departing from the scope of the present invention. The following detailed description, therefore, is not to be taken in a limiting sense, and the scope of the present invention is defined by the appended claims.
It is to be understood that the features of the various exemplary embodiments described herein may be combined with each other, unless specifically noted otherwise.
Embodiments provide a semiconductor device including a convertible polymer layer that is deposited on at least a portion of a chip and a carrier of the semiconductor device, where the convertible layer is deposited as an electrically conducting layer and subsequently converted to an electrically insulating layer.
Embodiments provide depositing an electrically conducting layer over portions of a chip and a carrier, where the electrically conducting layer is suited for receiving a metallization layer useful in establishing electrical connection to the chip. After the metallization layer is deposited, the electrically conducting layer is converted to an electrically insulating layer.
Embodiments provide a polymer layer that is deposited onto portions of a chip and a carrier, where the polymer layer is configured to be structured and/or patterned to include metallized traces or other forms of connection. In one embodiment, the polymer layer includes a dopant or other activating agent that configures the polymer layer to be electrically conducting. A metallized layer is applied to the doped/activated polymer layer, after which the doped/activated polymer layer is deactivated or “de-doped” to convert the polymer layer to an electrically insulating layer. Activation of the polymer layer to an electrically conducting state is accomplished without having to seed the polymer layer, which can be expensive and include additional process steps. Thus, the electrically conducting is suited for melt processing in its conducting state. Deactivation of the doped polymer layer is accomplished with low temperature or other processes that are consistent with semiconductor fabrication.
Process 20 (
In one embodiment, ECL 40 is provided as an organic conductive polymer that is doped to introduce charge carriers and provide the organic conductive polymer with an electrical conductivity similar to silver (105 S/cm). Suitable such organic conductive polymers include polythiophene, polyppyrrole, polysulfonen, polyaniline, polyindophenine, polystyrene derivatives, and PEDT or poly (3,4-ethylendioxythiophen) that are doped and/or activated to an electrically conducting state by electron addition or electron removal.
Suitable such organic conductive polymers that are activated to an electrically conducting state include conjugated chains having sp2 hybridized carbons. For example, polyacetylene is a conjugated polymer (CH)x having three in-plane sigma-orbitals of sp2 hybridized carbon that form a backbone. Two of the three in-plane sigma-orbital are bonded to neighboring carbons and the third sigma-orbital is bonded to a hydrogen atom. A fourth electron resides in the pz orbital and is orthogonal to the plane defined by the other three sigma bonds and is called a pi-electron. The pi-electron on the neighboring carbons forms a weak pi-pi bond of an alternating bond structure. Consequently, polyacetylene is a semiconductor with low electrical conductivity in its ground state. The electrical conductivity of polyacetylene (and other such suitable organic conductive polymers) is increased by a factor of up to 108 by doping with charge carriers to form doped conjugate polymers or conducting polymers. In one example, oxidation of polyacetylene with iodine results in a 108 increase in electrical conductivity for the polymer system.
Another suitable organic conductive polymer that is activated to an electrically conducting state includes an endowed form of PEDT identified as Baytron® M available from Bayer AG.
The doping of the organic conductive polymer with charge carriers (by the addition or removal of electrons) increases the electrical conductivity of the material. In one embodiment, the organic conductive polymer provides is an electrical insulator before the polymer is doped and has an electrical conductivity on the order of 10−8 S/cm. Upon doping, the conjugated polymer has electrical conductivity that is increased by a factor of up to 108 S/cm even at a very low doping level of less than one percent.
Doping of the organic conductive polymer to form ECL 40 includes chemical doping and electro-chemical doping. In one embodiment, the organic conductive polymer is chemical doped by exposing the polymer to an oxidant (for example iodine or bromine) or a reductant such as an alkali metal. In one embodiment, the polymer is electrochemically doped to form ECL 40. In one embodiment, the semiconductor device including chip 30 and the organic conductive polymer layer coated on chip 30 is introduced into an electrolyte solution and exposed to an electric potential difference that causes a charge (and an appropriate counter ion form the electrolyte) to enter the polymer in the form of electron addition (n-doping) or electron removal (p-doping). In general, chemical n-doping is conducted in an inert gas environment to prevent oxygen from reacting with the electron rich n-doped polymer.
In one embodiment, the selected organic conductive polymer is activated by electron addition/removal by introducing a molecule that acts as an electron donor to make the resulting polymer highly electrically conductive. Examples of suitable molecules configured to donate electrons to the organic conductive polymers include oxidizing agents or arsenpentafluorid. The addition of charge carriers from the addition or removal of electrons into the conduction or valence bands increases the electrical conductivity of the polymer dramatically. Suitable molecules for electron donation include melanin, iodine, or bromine
ECL 40 is deposited from the melt or in solution onto a portion of chip 30 and a portion of carrier 32 in an electrically conducting state. ECL 40 has thermal stability of greater than 250 degrees Celsius and when doped has a high specific conductivity of about 10−3 Ohm/cm. ECL 40 is, as such, suited for deposition as a conductive strip on semiconductor devices and printed circuit boards. As examples, ECL 40 is deposited onto chip 30 and carrier 32 by dipping, spin coating, spraying, dispersion, printing, or other suitable forms of deposition. ECL 40 has an affinity and forms a strong bond with other conducting materials, such as metal carriers.
In accord with both
In one embodiment, metal layer 50 is provided as a single layer of metal such as copper, silver, aluminum, gold, or alloys of these metals. In one embodiment, metal layer 50 is provided as multiple layers of such metals and/or compositions of such metals and deposited on ECL 40 and a portion of chip 30 and carrier 32.
Deposition and bonding of metal layer 50 to ECL 40 is enhanced by the electrical conductivity of ECL 40. Metal layer 50 is applied to ECL 40 in a suitable deposition process, such as printing, spraying, galvanic deposition, electrolytic deposition, dipping, or printing.
In one embodiment, conversion process 60 is configured to deactivate or de-dope the charge carrier introduced into ECL 40 (
In one embodiment, conversion process 60 provides a thermal bath configured to heat and deactivate charged carriers in ECL 40 (
In one embodiment, conversion process 60 includes a laser or other light source configured to deactivate charge carriers in ECL 40 (
In one embodiment, conversion process 60 is configured to chemically deactivate charged carriers in ECL 40 (
In one embodiment, conversion process 60 converts that portion of ECL 40 that is not covered by mask 82 into an electrically insulating state. In one embodiment, conversion process 60 converts that portion of ECL 40 that is covered by mask 82 into an electrically insulating state. That is to say, mask 82 includes positive masks and negative masks depending upon the application.
Embodiments provide a semiconductor device including a chip, for example a power chip or a power transistor, attached to a carrier and including a convertible layer deposited on the chip and the carrier. The convertible layer is deposited in an electrically conducting state and is configured for structuring and/or patterning subsequent to being converted to an electrically insulating state.
Although specific embodiments have been illustrated and described herein, it will be appreciated by those of ordinary skill in the art that a variety of alternate and/or equivalent implementations may be substituted for the specific embodiments shown and described without departing from the scope of the present invention. This application is intended to cover any adaptations or variations of the specific embodiments of semiconductor devices including a layer that is convertible between electrically conducting and electrically insulating states, as discussed herein. Therefore, it is intended that this invention be limited only by the claims and the equivalents thereof.
| Number | Name | Date | Kind |
|---|---|---|---|
| 5457862 | Sakata et al. | Oct 1995 | A |
| 6674635 | Fife et al. | Jan 2004 | B1 |
| 7443019 | Bauer et al. | Oct 2008 | B2 |
| 20050039840 | Foster et al. | Feb 2005 | A1 |
| 20050046001 | Warner | Mar 2005 | A1 |
| 20070034997 | Bauer et al. | Feb 2007 | A1 |
| 20070040260 | Otremba | Feb 2007 | A1 |
| 20090127547 | Luebben et al. | May 2009 | A1 |
| 20090167288 | Reid et al. | Jul 2009 | A1 |
| 20100187700 | Weidner | Jul 2010 | A1 |
| Number | Date | Country |
|---|---|---|
| 102005037321 | Feb 2007 | DE |
| 102006040724 | Mar 2008 | DE |
| Number | Date | Country | |
|---|---|---|---|
| 20100200978 A1 | Aug 2010 | US |