This invention relates generally to semiconductor pressure sensor devices and more particularly to the provision of contact systems for such devices that are suitable for exposure to harsh chemical and thermal environments.
Semiconductor devices, such as semiconductor based pressure sensors, have been used in harsh environments such as in the acidic automotive exhaust gas environment. In the case of piezoresistive pressure sensors, electrically conductive metallization has been utilized to enable electrical connection from the sensor housing, typically by means of wire bond connections, to the ohmic contact of the sensor which is electrically connected via doped silicon to the piezoresistive portion of the pressure sensor.
The use of semiconductor-based pressure sensors in harsh environments is often limited by the susceptibility of the commonly used aluminum based metallization to corrosion that can occur in acidic environments. Various approaches have been taken to deal with this problem. One approach is shown in U.S. Pat. No. 6,651,508, in which the sensor and wire bonds are covered with gel in an effort to protect the sensor from corrosion. However, the gel is permeable to acids and moisture, therefore, if the metallization system is not inherently robust to the media to which it is exposed, the sensor will eventually fail due to corrosion.
The challenges related to metal corrosion of semiconductor-based pressure sensor exposed to harsh environments are discussed in U.S. Pat. Nos. 6,584,853; 6,030,684 and 6,085,596 which, unlike the present invention, do not disclose electrically conductive and corrosion resistant metal contact systems. Instead, these patents disclose various sensor coating and packaging techniques for protecting the underlying metallization resulting in larger and/or more expensive semiconductor sensors than desired. For instance, the electrically insulating layer used in '596 does not cover the aluminum bond pads which forces packaging schemes (see
U.S. Pat. No. 6,107,170 discloses a gold, titanium-tungsten metallization to address the aluminum metallization corrosion problem. However, the titanium-tungsten layer is subject to corrosion when exposed to certain exhaust gas environments through imperfections in the gold layer and at exposed edges of the titanium-tungsten layer.
An object of the present invention is the provision of a corrosion resistant electrical contact system for semiconductor pressure sensors free of the prior art limitations noted above. Another object is the provision of a corrosion resistant, low cost electrical contact system for use with semiconductor-based pressure sensors suitable for exposure to harsh acidic and thermal environments. Yet another object of the invention is the provision of a low cost electrical contact system for semiconductor-type pressure sensors suitable for use in an automotive exhaust system.
In accordance with the teachings of the present invention, a semiconductor substrate, doped with impurities to make it suitable for piezoresistive pressure-sensing and formed typically with glass passivation layers, is patterned to expose regions of the doped semiconductor for the placement of metal electrical contacts. A suitable ohmic contact layer, such as platinum silicide or tantalum silicide, is formed in the exposed region of the doped semiconductor and a layer of tantalum is deposited over the ohmic contact layer and typically also over the passivation layers using any suitable method to form a dense film. The corrosion resistance of tantalum is exceptional. Unlike aluminum and titanium-tungsten, tantalum is virtually inert to all acids below 150 degrees C., with the exception of hydrofluoric acid which is not a concern in most applications. In most cases, it is preferred to add one or more layers of corrosion resistant material such as platinum or other precious metals, such as gold, palladium, iridium, rhodium or ruthenium, that are more conducive than tantalum to conventional electrical connection techniques, such as wire bonding, for connecting the semiconductor pressure sensor to a sensor package.
Other objects, advantages and details of the electrical contact systems appear in the following detailed description of preferred embodiments of the invention, the detailed description referring to the drawings in which:
Reference made to upper, lower and the like layers throughout the specification and claims refer to the orientation of layers shown in the drawings.
With reference to
Tantalum is an element of Group V B of the periodic table. As reported in “Tantalum as a material of construction for the chemical and processing industry—A critical survey” by U. Gramberg, M. Renner and H. Diekmann, Materials and Corrosion 46, pages 691, 692 (1995), “due to their electronic configuration, metals of this Group and the neighboring Group IV and VI B are strongly electronegative, therefore called ‘reactive’ metals. . . . On the other hand, high reactivity also leads to the formation of extremely stable oxide at ambient temperatures as well, thus providing a necessary prerequisite for general chemical inertness. However, to protect the metal, the oxide layer has to bond strongly to the metal, be free of defects, be very thin in order to cause only a low level of internal stresses, and form spontaneously in case of damage. All conditions are fulfilled by tantalum and its oxide Ta205, resulting in the interesting phenomenon of a highly reactive metal possessing an extreme chemical inertness.”
The tantalum layer 24 could, if desired, be replaced with a layer of niobium 30. Niobium, like tantalum, is an element of Group V B; its physical and chemical properties resemble those of tantalum and it is nearly as corrosion resistant as tantalum.
Precious, corrosion resistant metals, such as platinum and gold, typically do not adhere well to the passivation layers, hence the advantage provided by the tantalum layer which serves as an adhesion layer between the precious metals and the passivation layers. Tantalum adheres well to silicon glass layers such as silicon nitride and silicon dioxide. It should also be noted that the tantalum layer can also serve as a diffusion barrier, for example, to gold.
The superior chemical robustness of the platinum tantalum metallization to harsh acidic environments was demonstrated by several tests. For example, in one test, piezoresistive pressure sensors with aluminum metallization, piezoresistive pressure sensors with gold titanium-tungsten metallization, and piezoresistive pressure sensors with platinum tantalum metallization were coated with Sifel 8070, a gel manufactured by Shin-Etsu, and immersed at 80 degrees C. in a 10.11 M hydrochloric acid solution. Aluminum sensors were removed from the solution after 2 hours and SEM analysis showed extensive corrosion of the aluminum metallization. Gold titanium-tungsten sensors and platinum tantalum sensors were removed form the solution after 120 hours and SEM analysis showed extensive corrosion of the gold and titanium-tungsten layers but no sign of corrosion of the platinum tantalum metallization.
In another test, piezoresistive pressure sensors with aluminum metallization, piezoresistive pressure sensors with gold titanium-tungsten metallization and piezoresistive pressure sensors with platinum tantalum metallization were immersed, at 80 degrees C., in a solution of 5.02 M sulfuric acid and 4.97 M nitric acid. Aluminum sensors were removed from the solution after 90 minutes and SEM analysis showed extensive corrosion of the aluminum metallization. Gold titanium-tungsten sensors and platinum tantalum sensors were removed from the solution after 16 hours and SEM analysis showed extensive corrosion of the gold titanium-tungsten metallization and no sign of corrosion of the platinum tantalum metallization.
Metallization of a platinum tantalum contact system can be fabricated with conventional semiconductor processes. By way of example, starting with a semiconductor substrate:
pattern the passivation layers (e.g., silicon nitride over silicon dioxide) to expose vias for metal contacts,
form ohmic contacts in the vias; e.g., form platinum silicide by sputtering platinum, heat treating it to form platinum silicide and removing platinum from unwanted areas (e.g., by ion beam milling)
deposit a layer of tantalum by sputtering (or other deposition procedures that yield a dense film) approximately 500 angstroms thick and then deposit in-situ, to prevent oxidation of the tantalum, a layer of platinum of approximately 4000 angstroms thick
pattern the platinum tantalum metal layer with conventional photo-lithography processes (spin photo-resist, cure it, expose it to UV light and develop it)
remove Pt and Ta layers from unwanted areas (e.g., by ion beam milling or reactive ion etching)
dissolve the photo resist (metal etch mask).
Although the present invention has been described and illustrated through several preferred embodiments thereof, it is to be understood that the invention is not to be so limited since changes and modifications may be made therein which are within the intended scope of the invention as hereinafter claimed. For example, the tantalum layer 24 or niobium layer 30 could, if desired, be replaced by a layer of tantalum alloy or niobium alloy respectively. Also, the top platinum layer 26 could, if desired, be replaced or augmented with one or more layers of the following precious metals or alloys of these metals: gold, iridium, palladium, ruthenium or rhodium. Furthermore, instead of silicides, a sufficiently highly doped surface region of the semiconductor substrate could be utilized to achieve good ohmic contact.
Although the present invention has been described for use in a piezoresistive pressure sensor, the benefits of the disclosed metallization systems have obvious applications in other semiconductor-based pressure sensing technologies such as capacitive.