Gallium Nitride (GaN) has electrical and physical properties that make it highly suitable for high frequency (HF) devices such as microwave devices. The HF devices produce a high amount of heat requiring a heat spreader to be attached to the HF devices to avoid device failure. One such heat spreader is diamond. A hot filament chemical vapor deposition (CVD) process has been used to form diamond that is used on GaN layers. Generally, these diamond layers are not deposited directly onto the GaN layers but onto some other material (e.g., silicon, silicon carbide, and so forth) that is eventually disposed with the GaN layer.
In one aspect, a method includes fabricating a gallium nitride (GaN) layer with a first diamond layer having a first thermal conductivity and a second diamond layer having a second thermal conductivity greater than the first thermal conductivity. The fabricating includes using a microwave plasma chemical vapor deposition (CVD) process to deposit the second diamond layer onto the first diamond layer.
In another aspect, a method includes fabricating a gallium nitride (GaN) layer with a first diamond layer having a first thermal conductivity and a second diamond layer having a second thermal conductivity greater than the first thermal conductivity. The fabricating includes using a microwave plasma chemical vapor deposition (CVD) process to deposit the second diamond layer of between about 2 mils to about 4 mils on the first diamond layer of less than about 1 mil.
In a further aspect, a device includes a gallium nitride (GaN) layer, a first layer of diamond having a first thermal conductivity disposed on the GaN layer and a second layer of diamond having a second thermal conductivity twice the first thermal conductivity deposited on the first layer of diamond.
Hot filament chemical vapor deposition (CVD) processes have been used to form diamond layers of less than 1 mil that are used on gallium nitride (GaN) layers. To be effective as a heat spreader, diamond layers must be greater than 2 mils. Moreover, the hot filament CVD process by its very nature produces a blackish-color diamond which is contaminated with material used in the hot filament CVD process such as tungsten, for example. In general, these “dirty” diamond layers that are produced have a lower thermal conductivity than pure diamond. In general, the thermal conductivity of diamond layers using the hot filament CVD process is about 800 to 1000 Watts/meter-Kelvin (W/m-K).
A microwave plasma CVD process has been known to produce much thicker diamond layers on the order of 4 mils or greater at a much faster rate than the hot filament CVD process. Moreover the diamond layers are purer than the hot filament CVD process producing diamond layers having a thermal conductivity greater than 1500 W/m-K. In one example, the thermal conductivity of diamond produced using the microwave plasma CVD process is twice the thermal conductivity of diamond produced using the hot filament process. However, the CVD processes including the microwave plasma CVD process is relatively unknown with respect to direct deposition onto GaN. For example, the deposition of diamond using hot filament CVD is typically done onto some other material (e.g., silicon, silicon carbide, and so forth) that is eventually is disposed with the GaN layer. Since the deposition of diamond directly onto to GaN using the microwave plasma CVD process is relatively unknown, the costs of developing and testing a reliable and successful processes to deposit diamond directly onto the GaN is extremely expensive. One way around the cost and expense of developing a process to deposit diamond directly onto GaN, is to deposit diamond using the microwave plasma CVD process onto an inferior diamond layer that was fabricated using the hot filament CVD, for example.
As used herein GaN layers may include pure GaN, doped GaN or GaN combined with other elements (e.g., AlGaN) or any combination thereof. Silicon substrates may include pure silicon, doped silicon, silicon dioxide, silicon carbide or any combination of silicon with other elements or any combination thereof.
Referring to
Referring to
Referring to
Referring to
The silicon/GaN structure 250 is immersed in a solution and subjected to ultrasound (302). By treating the surface prior to deposition (e.g., a processing block 314), the diamond layer 316 has a better chance of forming on the GaN 16 during deposition. In one example, the solution is an isopropyl alcohol solution that includes diamond particles (e.g., nano-diamond particles (10−9 m)).
The third diamond layer 316 is disposed on the silicon/GaN structure 250 (314) (
The first and second diamond layers 14, 12, formed using process blocks 212, 214 and 218, for example, are attached to the remaining GaN/diamond structure to form a diamond/GaN/diamond/diamond structure 360 (334) (
Referring to
Referring to
In one example, a device 400 (e.g., a HEMT device) includes a source 404, a drain 406 and a gate 408 (e.g., a T-Gate) that are deposited in a metallization step onto to the surface 302 of the GaN layer 16. The gate 408 is formed in the diamond layer 316 after removal of portions of the diamond layer thereby exposing the GaN. In this example, the removal of portions of the diamond layer 316 splits the diamond layer into two diamond layers 316a, 316b each having a width W. In this configuration, the diamond layers 316a, 316b may function as a dielectric layer and a heat spreader by removing the heat away from the gate 408. In some examples, the widths of the diamond layers 316a, 316b may not be equal. In one example, portions of the gate 408 are adjacent to and in contact with the diamond layers 316a, 316b and other portions of the gate 408 form gaps 410a, 410b (e.g., air gaps) between the gate and the diamond layers 316a, 316b. In one example, gate 408, the gaps 410a, 410b, the diamond layer 316a, 316b form capacitance structures. One of ordinary skill in the art would be aware of several methods to form these gaps 410a, 410b. For example, prior to metallization to form the gate 408, a material (e.g., photoresist) may be on the surface of the diamond layer 316. After the gate 408 is formed, the material is removed forming the gaps 410a, 410b. In other examples, the device 400 does not include gaps 410a, 410b so that the gate 408 is directly on the surface of the diamond layers 316a, 316b. In still further examples, other materials may fill gaps 410a, 410b that may or may not contribute to capacitance.
Referring to
The processes described herein are not limited to the specific embodiments described herein. For example, the processes are not limited to the specific processing order of the process steps in
While the invention is shown and described in conjunction with a particular embodiment having an illustrative product having certain components in a given order, it is understood that other embodiments well within the scope of the invention are contemplated having more and fewer components, having different types of components, and being coupled in various arrangements. Such embodiments will be readily apparent to one of ordinary skill in the art. Other embodiments not specifically described herein are also within the scope of the following claims.
Number | Name | Date | Kind |
---|---|---|---|
5252840 | Shiomi et al. | Oct 1993 | A |
5277975 | Herb et al. | Jan 1994 | A |
5633516 | Mishima et al. | May 1997 | A |
5726463 | Brown et al. | Mar 1998 | A |
5962345 | Yen et al. | Oct 1999 | A |
6255712 | Clevenger et al. | Jul 2001 | B1 |
20030170458 | Noguchi | Sep 2003 | A1 |
20050139838 | Murata et al. | Jun 2005 | A1 |
20060081985 | Beach et al. | Apr 2006 | A1 |
20060113546 | Sung | Jun 2006 | A1 |
20070126026 | Ueno et al. | Jun 2007 | A1 |
20070272929 | Namba et al. | Nov 2007 | A1 |
20080181550 | Earnshaw | Jul 2008 | A1 |
20080206569 | Whitehead et al. | Aug 2008 | A1 |
20090146186 | Kub et al. | Jun 2009 | A1 |
20100001292 | Yamasaki et al. | Jan 2010 | A1 |
20100155900 | Korenstein et al. | Jun 2010 | A1 |
20100187544 | Korenstein et al. | Jul 2010 | A1 |
20100216301 | Chen et al. | Aug 2010 | A1 |
Number | Date | Country |
---|---|---|
0 457 508 | Nov 1991 | EP |
2 015 353 | Jan 2009 | EP |
2005 210105 | Aug 2005 | JP |
2005 210105 | Aug 2005 | JP |
WO 2006117621 | Nov 2006 | WO |
WO 2007122507 | Nov 2007 | WO |
WO 2008147538 | Dec 2008 | WO |
Number | Date | Country | |
---|---|---|---|
20100155901 A1 | Jun 2010 | US |