Process of forming epitaxial substrate and semiconductor device provided on the same
10840091 ยท 2020-11-17
Assignee
Inventors
Cpc classification
H01L29/7787
ELECTRICITY
H01L29/66462
ELECTRICITY
H01L29/205
ELECTRICITY
H01L21/0262
ELECTRICITY
H01L29/7786
ELECTRICITY
International classification
H01L21/02
ELECTRICITY
H01L29/778
ELECTRICITY
H01L29/205
ELECTRICITY
Abstract
A process of forming a nucleus fanning layer in a nitride semiconductor epitaxial substrate is disclosed. The process includes steps of growing: a lower layer of the nucleus forming layer on a substrate; an upper layer of the nucleus thrilling layer on the lower layer; and a nitride semiconductor layer each by the metal organic chemical vapor deposition (MOCVD) technique. The growth of the nitride semiconductor layer is done at a temperature lower than a growth temperature for the upper layer, and the growth of the upper layer is done by supplying ammonia (NH.sub.3) at a flow rate greater than the flow rate of ammonia (NH.sub.3) timing the growth of the lower layer.
Claims
1. A process of forming an epitaxial substrate including a substrate, the process comprising steps of: growing a lower layer made of aluminum nitride (AlN) with aluminum (Al) as a group III element and nitrogen (N) as a group V element on the substrate by a metal organic chemical vapor deposition (MOCVD) technique at a source gas flow rate for the group III element and a source gas flow rate for the group V element in a first III/V ratio; growing an upper layer made of AIN by the MOCVD technique at a source gas flow rate for the group III element and a source gas flow rate for the group V element in a second III/V ratio; and growing a nitride semiconductor layer on the upper layer under a growth temperature lower than a growth temperature for the upper layer, wherein the lower layer and the upper layer provide an AIN nucleus forming layer, the upper layer having a thickness that is 5 nm at most and that is smaller than a thickness of the lower layer on the substrate, wherein the second III/V ratio is smaller than the first III/V ratio, and wherein ammonia (NH.sub.3) continuously is supplied after completion of growing of the lower layer and before beginning growing of the upper layer.
2. The process according to claim 1, wherein the growth temperature for the nitride semiconductor layer is at least 30 C. lower than the growth temperature for the upper layer.
3. The process according to claim 1, further including a step of, after the step of growing the upper layer but before the step of growing the nitride semiconductor layer, supplying a source material for nitrogen (N) within an apparatus for the MOCVD technique.
4. The process according to claim 1, wherein, in the step of growing the upper layer, the flow rate of the source material for Al is decreased in comparison with the flow rate of the source material for Al in the lower layer.
5. The process according to claim 1, wherein the step of growing the lower layer grows the lower layer with a thickness at least 5 nm.
6. The process according to claim 1, wherein the step of growing the nitride semiconductor layer grows a layer made of gallium nitride (GaN) under the growth temperature lower than the growth temperature of the upper layer.
7. The process according to claim 1, wherein, in the step of growing the upper layer, the flow rate of the source material for nitrogen (N) is at least 5 standard liters per minutes (slm) and higher than the flow rate of the source material for nitrogen (N) during growth of the lower layer.
8. The process according to claim 1, wherein the upper layer has a nitrogen rich composition.
Description
BRIEF DESCRIPTION OF DRAWINGS
(1) The foregoing and other purposes, aspects and advantages will be better understood from the following detailed description of a preferred embodiment of the invention with reference to the drawings, in which:
(2)
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DESCRIPTION OF EMBODIMENT
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(7) Specifically, the lower layer 11a is provided on and in contact with the substrate 10, while, the upper layer 11b is provided on and in contact with the lower layer 11a. The GaN layer 12 is provided on the upper layer 11b, the barrier layer 14 is provided on the GaN layer 12, and the cap layer 16 is provided on the barrier layer 14. The electrodes of the source 13, the drain 15, and the gate 17 are provided on the cap layer 16.
(8) The substrate 10 may be made of silicon carbide (SiC). The lower layer 11a is made of aluminum nitride (AlN) with a thickness of 10 nm, while, the upper layer 11b is also made of AlN but with a thickness thinner than that of the lower, which is 3 nm in the present embodiment. Although the lower layer 11a may have a stoichiometric composition, the upper layer 11b has a non-stoichiometric composition, exactly an N-rich composition.
(9) The channel layer 12 may be made of un-doped gallium nitride (GaN) with a thickness of around 600 nm, where a lower portion of the GaN layer 12 may be operable as a buffer layer 12a, while, an upper portion thereof may be operable as a channel layer 12b. The barrier layer 14, which may be made of aluminum gallium nitride (AlGaN) with an aluminum composition of 0.22, has a thickness of 24 nm and forms or induces the channel in the channel layer 12b at the interface against the barrier layer 14. The cap layer 16, which may be made of n-type GaN, has a thickness of 5 nm.
(10) The source electrode 13 and the drain electrode 15 may be formed from a stacked metal of tantalum (Ta), aluminum (Al), and tantalum (Ta), which may be denoted as Ta/Al/Ta, from a side of the cap layer 16; that is, the source electrode 13 and the drain electrode 15 may be formed by alloying the stacked metal above described. The gate electrode 17 may also provide a stacked metal of, from the side of the cap layer 16, nickel (Ni), palladium (Pd), gold (Au), and tantalum (Ta), which may be denoted as Ni/Pd/Au/Ta, where the nickel (Ni) makes a Schottky contact against the cap layer 16.
(11) Table 1 below summarizes growth conditions of the epitaxial substrate 110 for the semiconductor device 100. In table 1, TMA, TMG, NH.sub.3, SiH.sub.4 mean tri-methyl-aluminum, tri-methyl-gallium, ammonia, and silane, respectively. Also in table 1, one (1) Torr is equal to 133.3 pascal (Pa), one (1) sccm (standard cc per minutes) is equal to 1.66710.sup.8 m.sup.3/s, and one (1) slm (standard liter per minutes) is equal to 1.66710.sup.11 m.sup.3/s, respectively.
(12) TABLE-US-00001 TABLE 1 growth conditions thickness pressure temperature source layer (nm) (Torr) ( C.) flow rates lower layer 11a 10 100 1100 TMA: 130 sccm NH.sub.3: 15 slm upper layer 11b 3 TMA: 130 sccm NH.sub.3: 20 slm GaN layer 12 600 1060 TMG: 54 sccm NH.sub.3: 20 slm barrier layer 14 24 TMG: 30 sccm TMA: 90 sccm NH.sub.3: 20 slm SiH.sub.4: 8 sccm cap layer 16 4 TMG: 43 sccm NH.sub.3: 20 slm SiH.sub.4: 40 sccm
The lower layer 11a and the upper layer 11b are grown at a growth temperature of 1100 C. and a growth pressure of 100 Torr, but the lower layer 11a is grown by supplying ammonia (NH.sub.3) with a flow rate of 15 slm; while, the upper layer 11b is grown with a flow rate of NH.sub.3 of 20 slm that is increased by 5 slm from that in the lower layer 11a.
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(14) The process first sets the temperature of the substrate 10 to be 1100 C. Supplying ammonia (NH.sub.3) with the flow rate of 15 slm and TMA 10 with the flow rate of 130 sccm, the lower layer 11a made of AlN is grown on the substrate 10 during the period from t.sub.1 to t.sub.2 by a thickness of 10 nm. Then, interrupting the supplement of TMA, the process increases the flow rate of ammonia (NH.sub.3) from 15 to 20 slm but continuously flowing nitrogen (N), which operates as a carrier gas, as keeping the temperature of the substrate 10 to be 1100 C. during the period from t.sub.2 to t.sub.3. At the instant t.sub.3 where the flow of ammonia (NH.sub.3) becomes stable, the growth of the upper layer 11b begins by supplying TMA with the flow rate of 130 sccm until the upper layer 11b has a thickness of 3 nm. Thus, the process decreases a ratio of the flow rates of a source gas for the group III element, namely aluminum (Al), against the flow rate of the source gas for the group V element, namely nitrogen (N), where the ratio of the flow rates of the source gases is often denoted as a III/V ratio.
(15) Thereafter, the process lowers the temperature of the substrate 10 down to 1060 C. during a period from t4 to t5, as shown in
(16) The first embodiment of the process of forming the semiconductor device 100 thus described increases the supplement, or the flow rate of ammonia (NH.sub.3) as the source gas for nitrogen (N) during the growth of the upper layer 11b, which means that the nitrogen composition in the upper layer 11b becomes larger compared with that of the lower layer 11a, which is sometimes called as an N-rich composition. Because the growth temperature for the GaN layer 12 is lower than that for the upper layer 11b, the process is necessary to lower the temperature of the substrate 10 after the growth of the upper layer 11b but before the growth of the GaN layer 12, during which the substrate 10, exactly, the surface of the upper layer 11b is exposed to a high temperature atmosphere and the upper layer 11b possibly dissociates nitrogen (N) from the surface thereof. The N-rich composition of the upper layer 11b may effectively compensate the dissociation of nitrogen (N) and suppress defects caused by the dissociation of nitrogen (N), which may also suppress defects induced in the layers grown on the upper layer 11b. Thus, the drain leak current caused by the defects may be effectively reduced.
(17) A process may increase the supplement of ammonia (NH.sub.3) during not only the growth of the upper layer 11b but the growth of the lower 11a to increase the nitrogen composition. However, when the nucleus forming layer 11 has an N-rich composition in a whole thereof, the growth for the semiconductor stack 19 on the AlN nucleus forming layer 11 varies the growth mode thereof and degrades crystal quality thereof. Thus, the process may divide the growth of the nucleus forming layer 11 into the lower layer 11a on the substrate 10 and the upper layer 11b on the lower layer 11a, where the lower layer 11a has a substantially stoichiometric composition between aluminum (Al) and nitrogen (N), while the upper layer 11b has the N-rich composition by increasing the supplement, or the flow rate of ammonia (NH.sub.3).
(18) The nucleus forming layer 11 is preferably grown under relatively higher temperature to decrease pits appearing on a grown surface thereof. Accordingly, the growth temperature for the nucleus forming layer 11 is preferably higher than 1100 C. While, the GaN layer 12 is preferably grown under a relatively lower temperature to suppress the dissociation of nitrogen (N) from the surface thereof. Accordingly, the growth temperature for the GaN layer 12 is preferably lower than that for the nucleus forming layer 11, typically around 1060 C. However, those conditions for the nucleus forming layer 11 and the GaN layer 12 are optional. For instance, the growth temperature for the GaN layer 12 is preferably lower than that for the nucleus forming layer 11 by at least 30 C. The difference in the growth temperatures may be 40 C. or greater in the present embodiment. The difference in the growth temperature inevitably accompanies with a lowering of a temperature after the growth of the upper layer 11b. As the difference in the growth temperatures becomes larger, a period to lower the temperature and stabilize thereat becomes longer, which means that a period for the upper layer 11b to be exposed in a high temperature becomes longer and nitrogen (N) is possibly dissociated from the surface of the upper layer 11b. The embodiment of the present embodiment, because of the N-rich composition of the upper layer 11b, may effectively suppress the defects caused in the surface of the upper layer 11b.
(19) The supplement, or the flow rate of ammonia (NH.sub.3) during the growth of the upper layer 11b is preferably greater than 20 slm, which may form the N-rich composition in the upper layer 11b and suppress the defects due to the dissociation of nitrogen (N) from forming in the upper layer 11b. The process may increase the supplement, or the flow rate of ammonia (NH.sub.3) as a difference in the growth temperatures between the upper layer 11b and the GaN layer 12 becomes larger in order to enhance the nitrogen composition in the upper layer 11b. Preferably, the flow rate of ammonia (NH.sub.3) for the upper layer 11b is greater than that for the lower 11a by at least 5 slm.
(20) In order to enhance the quality of the semiconductor stack 19 grown on the nucleus forming layer 11, the semiconductor stack 19 preferably decreases lattice miss-matchings against the substrate 10. Accordingly, the present embodiment provides the lower layer 11a whose lattice constant is closest to that of the substrate 10 and has a substantial thickness, which may be thicker than, for instance, 5 nm or a thickness greater than 10 nm is further preferable. The semiconductor stack 19 should be grown on a semiconductor surface with lesser pits that could accelerate the dissociation of nitrogen (N). Accordingly, the upper layer 11b preferably has a thickness greater than 3 nm. The lower layer 11a may have a greater thickness than that of the upper layer 11b.
(21) The process of the present embodiment, as shown in
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(23) Second Embodiment
(24) A growth sequence according to the second embodiment of the invention decreases the supplement of TMA, which is a source gas for aluminum (Al), during the growth of the upper layer 11b. Table 2 summarizes the growth conditions for the epitaxial substrate 110A according to the second embodiment of the invention.
(25) TABLE-US-00002 TABLE 2 growth conditions thickness pressure temperature source layer (nm) (Torr) ( C.) flow rates 1.sup.st layer 11a 10 100 1100 TMA: 130 sccm NH.sub.3: 15 slm 2.sup.nd layer 11b 3 TMA: 80 sccm NH.sub.3: 20 slm GaN layer 12 600 1060 TMG: 54 sccm NH.sub.3: 20 slm barrier layer 14 24 TMG: 30 sccm TMA: 90 sccm NH.sub.3: 20 slm SiH.sub.4: 8 sccm cap layer 16 5 TMG: 43 sccm NH.sub.3: 20 slm SiH.sub.4: 40 sccm
As clearly listed in Table 2 above, the lower layer 11a and the upper layer 11b are grown under a temperature and a pressure common to those two layers, 11a and 11b. The lower layer 11a is grown by supplying ammonia (NH.sub.3) with a flow rate of 15 slm, while, the upper layer 11b is grown with a flow rate of 20 slm increased by 5 slm from that for the lower layer 11a. A feature of the second embodiment is that the flow rate of TMA for the upper layer 11b is decreased from the flow rate of TMA for the lower layer 11a by 50 sccm, where the former is 80 sccm while the latter is 130 sccm.
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(27) The second embodiment of the present invention may grow the upper layer 11b with the N-rich composition, which may reduce the drain leak current. Besides, the flow rate of TMA during the growth of the upper layer 11b is decreased from that during the growth of the lower layer 11a, which may reduce the growth rate of the upper layer 11b compared with the growth rate of the lower layer 11a. Accordingly, the process may precisely control a thickness of the upper layer 11a. For instance, an upper layer 11b having a limited thickness of 3 nm may be grown uniformly and precisely.
(28) Modification of the second embodiment is shown in
(29) Third Embodiment
(30) The third embodiment of the present invention gradually increases the flow rate of ammonia.
(31) In the embodiment thus described, source materials and flow rates thereof are not restricted to those exemplarily described above. For instance, the flow rate of ammonia (NH.sub.3) may be greater than 20 slm or smaller than 15 slm. Further specifically, the lower layer 11a may be grown by supplying ammonia (NH.sub.3) with the flow rate thereof smaller than 15 slm, while, the upper layer 11b may be grown by supplying ammonia (NH.sub.3) with a flow rate greater than 20 slm. A key feature of the embodiment is that the flow rate of ammonia (NH.sub.3) for the upper layer 11b is greater than that for the lower layer 11a. Thus, the upper layer 11b may be grown as the N-rich composition, which may suppress the dissociation of nitrogen from the period t4 to t5, after the completion of the growth of the upper layer 11b but before the beginning of the growth of the GaN layer 12, during which the surface of the upper layer 11b is exposed to an ambient of a high temperature. The source material for nitrogen (N) is not restricted to ammonia (NH.sub.3), and that for aluminum (Al) is also not restricted to TMA. For instance, tri-ethyl-aluminum (TEA) may be applicable to a source material for aluminum (Al).
(32) The semiconductor device 100 thus formed may further provide an insulating film on the electrodes of the source 13, the drain 15, and the gate 17, and on the cap layer 16 between the electrodes, 13 to 17, to enhance moisture resistance of the semiconductor device 100, where such an insulating film is sometimes called as a passivation film. The insulating film may be made of silicon nitride (SiN), silicon oxy-nitride (SiON), and so on.
(33) Also, the semiconductor substrate 10 of the embodiment may provide other devices except for the FET or an active device, that is, the substrate may provide or integrate passive devices. The substrate 10 may provide other electrodes except for the source 13, the drain 15, and the gate 17, namely, those for passive devices and so on.
(34) The semiconductor stack 19 includes nitride semiconductors, such as, except for GaN and AlGaN, indium gallium nitride (InGaN), indium nitride (InN), indium aluminum nitride (InAlN), indium aluminum gallium nitride (InAlGaN), and so on. The substrate 10 may be, except for SiC, made of silicon (Si), sapphire (Al.sub.2O.sub.3), gallium nitride (GaN), and so on.
(35) Although the present invention has been described with reference to specific embodiments, ordinary person skilled in the art will recognize that changes may be made in form and detail without departing from the spirit and scope of the invention.