Patent Application
20060255432
This invention relates generally to semiconductor structures.
A complementary metal oxide semiconductor (CMOS) device is generally a delicate electronic structure formed by a combination of lithographic and etching techniques that allow the device to be formed and exist in a microscopically clean, contamination free environment with precisely controlled physical properties to ensure reliable and efficient high speed operation. As a result, there is a need to control the dielectric constant of materials used to separate the electronic components and interconnections within the device.
To this end, an interlayer dielectric (ILD) material is deposited around the structures (transistors, passives, etc.) and between the layers of interconnections that make up the CMOS device for the purpose of establishing a dielectric constant. The dielectric constant affects the speed with which signals may propagate through the interconnection of the device.
While many dielectric materials have been studied, for the lowest dielectric constants, increasing amounts of void space and hence air have been incorporated within ILD materials. Indeed, true air gaps have been engineered into the devices directly to optimize the lowest effective dielectric constants. Air gap structures may be formed and encapsulated to protect such structures from the deleterious effects of environmental contamination.
Similarly, in a variety of other circumstances, it may be desirable to form air gap structures in various microelectronic, micromechanical, microbiological, and microoptical systems, as well as, microelectromechanical system (MEMS) device.
Thus, there is a need to make airgaps in semiconductor structures.
Referring to
In some embodiments, the structure 10 may be a portion of a complementary metal oxide semiconductor (CMOS) integrated circuit. In other embodiments, it may be a portion of a microelectromechanical system.
The layer 14 may be driven off by heating the structure 10 after the capping layer 12 has been deposited on the surface of the polymer. The capping layer 12 can also serve as an etch stop for the creation of the next layer. If the layer 12 is porous, the thermally decomposed sacrificial layer 14 may be driven off without removing the layer 12. However, in other embodiments, apertures of any type may be formed in the layer 12 as desired.
As a result of the thermally driven decomposition and removal material of the forming the layer 14, an air gap region, pocket, or cavity 18 of low dielectric constant may be formed as shown in
Advantageously, the sacrificial layer 14 may be made of a material that may be decomposed by temperatures greater than those normally encountered during conventional semiconductor fabrication processes. A film that decomposes at relatively high temperatures (e.g., greater than about 260° C.) into smaller molecular weight effluents is advantageous. Advantageously, the decomposing film exhibits a high decomposition temperature and generally lower molecular weight byproducts on decomposition so that those byproducts can diffuse away through the layer 12.
The following chart provides a list of components and their thermal decomposition temperatures (Td):
In accordance with another embodiment of the present invention, the layer 12 may be sufficiently porous to facilitate the exhaustion of the decomposed sacrificial layer 14 upon heating. A thin layer of hydrogen silsesquioxane (HSQ) or methylsilsesquioxane (MSQ) spin-on glass (SOG) may be utilized as the capping layer 12. After being cured, the HSQ or MSQ layer 14 may be exposed to electron beam or plasma conditions to densify the HSQ or MSQ film to be like a silicon dioxide film.
In some cases, a silicon dioxide chemical vapor deposition layer may be applied as an option to seal all remaining pores in the HSQ or MSQ film for subsequent metal interconnect processes. The deposited silicon dioxide layer may enhance the mechanical properties of the HSQ or MSQ layer and/or seal the remaining pores in the HSQ or MSQ films.
In some embodiments, the stress that is caused on the layer 12 during decomposition may be reduced. HSQ or MSQ may be sufficiently porous to enhance the ability of the thermally decomposing polymers to diffuse out of the air gap pocket or cavity 18, through the layer 12, without building up pressure to excessively deform the layer 12. The layer 12 performance may be comparable to silicon dioxide films after electron beam or plasma treatment of the layer 12. In some cases the mechanical performance of the layer 12 may be enhanced by forming a sealing material, such as deposited silicon dioxide, on top of the HSQ/MSQ layer 12.
In some cases the receiving surface may be hydrophilic while the polymer decomposing film such as those described herein may be relatively hydrophobic. Because of the energy mismatch, when the decomposing film is applied over surface irregularities, such as trenches, there may be incomplete filling of those trenches or bridging.
As a result, it is desirable to energy match the decomposing film to the underlying surface. In other words, if the underlying surface or the polymer are not both hydrophilic or both hydrophobic, it may be desirable to convert one of the surfaces to energy match the other.
In the case of hydrophobic decomposing polymers such as those described previously herein, it may be most feasible to simply modify a hydrophilic surface to which they are to be applied to make that surface hydrophobic. Thus, referring to
In one embodiment, the surface 40 may be treated in the atmosphere of hexamethyldisilazane (HMDS) saturated nitrogen for 100 seconds at a temperature of 40° C. Following a cooling step, the surface 40 may be spin coated with the sacrificial polymer 46, as shown in
Other materials that may be utilized for surface energy modification include alkyl and fluoroalkyl functionalized silylhalides, alkoxysilanes, and nitrogen containing silation agents. With different types of substrates such as SiON, SiOF, carbon doped oxide (CDO), and metal, appropriate surface tension modifying agents may be utilized. These may include self-assembled monolayers (SAMs) formed from precursors including, but not limited to, thiols, sulfides, phosphates, phosphites, alkenes, chelation agents (benzotriazole (BTA), crown ethers, kryptands, cyclodextrins, poly and oligothiophenes, poly and oligoanalines) to mention a few examples.
While the present invention has been described with respect to a limited number of embodiments, those skilled in the art will appreciate numerous modifications and variations therefrom. It is intended that the appended claims cover all such modifications and variations as fall within the true spirit and scope of this present invention.
This application is a continuation of U.S. Patent application Ser. No. 10/353,506, filed on Jan. 28, 2003.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10353506 | Jan 2003 | US |
| Child | 11485078 | Jul 2006 | US |
