Background and Summary
The invention provide a method for epitaxially growing single crystalline silicon on a silicon substrate from a silicon-bearing gas at a temperature below the pyrolytic threshold of the gas and at temperatures below those normally required for epitaxial growth.
Low temperature, e.g. 400.degree. C., deposition and epitaxial growth of single crystalline silicon is known in the art, for example Schachameyer et al U.S. Pat. Nos. 4,655,849, 4,668,304, 4,670,063, 4,670,064, 4,685,976, incorporated herein by reference. Such low temperature is significantly below typical thermal processing temperatures of 1000.degree. C. In the latter type of processing, the silicon-bearing gas is heated above its pyrolytic threshold such that the gas thermally decomposes.
The present invention uses a combination of both thermal and photolytic activation of a siliconbearing gas to epitaxially grow single crystalline silicon. In the preferred embodiment, the process is carried out at 570.degree. C. This temperature is well below the temperature normally required for epitaxial growth, and thus avoids deleterious high temperature effects on the wafer substrate. Such temperature is above the strictly photolytic range, whereby to provide some of the beneficial effects of thermal processing.
The invention also involves the use of one or more intermediate substitute bonding agents which replace the silicon-oxygen bond of an oxidized silicon wafer substrate with one or more intermediate substitute bonds which are readily processed and ultimately replaced by a silicon-silicon bond as the silicon-bearing gas is thermally and photolytically decomposed to yield atomic silicon.
In the preferred embodiment, an oxidized silicon wafer substrate is fluorinated by immersing it in a solution of dilute hydrofluoric acid. This removes the oxide layer and substitutes an adsorbed fluorinated layer for the silicon-oxygen bond. The wafer substrate is then placed in a photo-CVD (chemical vapor deposition) chamber, and the chamber is evacuated to a sub-UHV (ultra high vacuum) level of 10.sup.-3 to 10.sup.-7 Torr. Hydrogen gas is introduced into the chamber, and excimer pulsed ultraviolet laser radiation is applied through the gas and against the substrate, generally perpendicularly thereto. The radiation photolytically removes the fluorinated layer and reduces the hydrogen to atomic hydrogen such that a silicon-hydrogen bond forms in place of the fluorinated layer. During this step, the wafer substrate is optionally heated to a temperature of about 570.degree. C., which thermally aids the reaction. Disilane gas is then introduced into the chamber, and, if not already heated, the wafer substrate is heated to a temperature of about 570.degree. C. Excimer pulsed ultraviolet laser radiation is applied through the gas and against the substrate, generally perpendicularly thereto. The thermal activation by the heating and the photolytic activation by the laser radiation in combination breaks the silicon-hydrogen bond and also decomposes the disilane gas to silane and an unstable intermediate compound SiH.sub.z which decomposes to hydrogen and atomic silicon. The atomic silicon bonds with the now unbonded silicon in the substrate to epitaxially grow single crystalline silicon thereon.
Brief Description of the Drawings
FIG. 1 illustrates the semiconductor processing technique in accordance with the invention.
FIG. 2 shows the chemical equations for the semiconductor processing technique in accordance with the preferred embodiment of the invention.
Detailed Description
FIG. 1 illustrates a method for epitaxially growing single crystalline silicon on a silicon wafer substrate 10. Excimer pulsed ultraviolet laser radiation is provided by laser 12 and homogenized by beam homogenizer 14. Substrate 10 is placed on a supporting susceptor pedestal 16 on resistance heater 18 in processing chamber 20, which is a conventional laser photo-CVD (chemical vapor deposition) reactor chamber. Reactant gas is introduced into chamber 20 at port 22 from sources 24 and 26, and is exhausted at port 28, all as is conventional. Chamber 10 typically has an inert gas purge window or port 30 through which excimer pulsed ultraviolet laser radiation from laser 12 through homogenizer 14 is introduced into chamber 20 along path 32 as directed by mirror 34 to impinge substrate 10 substantially perpendicularly thereto. The above noted incorporated patents show various available excimer pulsed ultraviolet laser radiation wavelengths and peak power, and an absorption spectrum of a reactant gas with absorption peaks at discrete designated excitation energy wavelengths. The excimer radiation wavelength is chosen according to the reactant gas absorption peaks, or vice versa, as noted in said patents.
The initial step in the process involves wet chemical cleaning, oxide removal and surface fluorination. Prior to loading silicon wafer substrate 10 into chamber 20, the wafer substrate is cleaned to remove both organic and metal contaminants and native oxide, SiO.sub.x, x=1, 2, which are present on the wafer surface upon exposure to ambient, i.e. room air. The known RCA clean recipe is employed to remove the organic and metal contaminants. The native oxide is stripped from the surface by dipping the wafer in dilute nHF, hydrofluoric acid, where n =an integer or a fraction thereof, effectively dissolving the SiO.sub.x, leaving behind a largely fluorinated surface, SiF.sub.y H.sub.z where y and z equal 1, 2, 3 or fractions thereof. This is illustrated at equations (1) and (2), FIG. 2. Fluorine has a stronger affinity to silicon than the affinity of oxygen to silicon.
The next step in the process involves dry, hydrogen reduction and/or surface halogenation with volatilization of regrown native oxide and photoinduced desorption of residual and/or reformed organic contamination. The wafer substrate is loaded into chamber 20 and cleaned once again using a low temperature uv, ultraviolet laser enhanced process. Native oxide may regrow on the substrate surface upon exposure to ambient room air between the dilute HF dip noted above and placement in chamber 20 and evacuated pump down thereof, equation (3), FIG. 2. This regrown native oxide film is removed by a photon enhanced hydrogen reduction process, to be described. Additionally, reformed organic contamination is volatilized during this step.
Reactor chamber 20 is evacuated, to be described, and substrate 10 is heated to 570.degree. C. Hydrogen gas is then flowed through the reactor from source 24 to a pressure of 20 Torr for 7 minutes. A 193 nm (nanometer), excimer laser 12 is then turned on, irradiating the surface of the silicon substrate at an intensity of 5 millijoules per square centimeter at 10 Hz for 3 minutes. Upon completion of this step, the substrate's surface is extremely clean and oxide-free, and a partially hydrogenated, SiH.sub.z, surface has now formed, equation (4), FIG. 2. The laser radiation removes the oxide layer. The combined thermal and photolytic activation breaks the silicon-fluorine bond and removes the fluorinated layer and reduces the hydrogen to atomic hydrogen such that the latter bonds with the silicon and forms a silicon-hydrogen bond to replace the silicon-fluorine bond and the fluorinated layer. In an alternative embodiment, the wafer substrate need not be heated, in which case the reaction relies upon photolytic activation by the laser radiation to break the silicon-fluorine bond and remove the fluorinated layer and reduce the hydrogen to atomic hydrogen. In a further alternative embodiment, the wafer substrate is heated to a different temperature to vary the thermal contribution to activation of the reaction.
The next step involves low temperature deposition of epitaxial silicon promoted by laser photolysis of disilane gas in a low pressure hydrogen atmosphere and laser enhanced desorption of hydrogen and laser enhanced adatom, silicon, mobility at the growing silicon surface. The substrate is maintained at 570.degree. C., and a dilute 5% mixture of disilane in hydrogen is flowed through the chamber at a pressure of 10 Torr. The laser 12 continues to irradiate the substrate as the film is grown. Film thickness is determined by the total time of this step. Deposition rate is controlled by the laser fluence, total reactor pressure and partial pressure of disilane in the reactor. The 193 nm laser 12 irradiates both the surface of substrate 10 and the disilane atmosphere above the surface of the substrate. The disilane gas photodissociates, forming silicon-containing intermediates which subsequently decompose, forming a silicon film at the substrate surface. As shown in equation (5), FIG. 2, the combined thermal and photolytic activation breaks the silicon-hydrogen bond and also decomposes the disilane Si.sub.2 H.sub.6 to silane SiH.sub.4 and an unstable intermediate SiH.sub.z, which latter then decomposes to hydrogen H.sub.2 and atomic silicon Si. The atomic silicon bonds with the now unbonded silicon in the wafer substrate to epitaxially grow single crystalline silicon thereon. Gas flow is ceased, and the substrate is cooled to room temperature either under vacuum or an inert gas atmosphere, He, Ar or N.sub.2
Typically, during processing in a photo-CVD reactor chamber such as 20, it is desirable to evacuate the chamber to levels approaching ultra high vacuum (UHV) conditions, 10.sup.-9 Torr and less. At this level, practically all residual water, air and organic gases are removed from the reactor chamber Under these conditions, the only contaminants which must be volatilized are the regrown native oxide and chemi/physisorbed organics. External heating of the entire reactor and the silicon wafer itself enables the adsorbed gases to more readily desorb, effectively reducing the time required to evacuate the reactor to UHV levels. However, a high temperature (greater than 750.degree. C.) cleaning or etching process is still required to volatized the native oxide and organic contamination.
The present invention does not require UHV conditions. This is particularly desirable, because obtaining UHV conditions is expensive and time consuming, especially when compared to the dry, laser driven hydrogen reduction cleaning process described above and illustrated at equation (4), FIG. 2. Also, the wafer does not have to be heated to temperatures is typically required to volatilize the oxide. For example, at atmospheric pressure with no vacuum 1200.degree. C. is typically required to clean the surface. At ultra high vacuum levels, e.g. 10.sup.-9 Torr, temperatures of 800.degree. C. are typically required to clean the wafer. In the present process, temperatures of only 570.degree. C. are used to clean the wafer. After evacuating the chamber to sub-UHV levels, 10.sup.-3 to 10.sup.-7 Torr, the silicon substrate is heated to 570.degree. C. in a flowing hydrogen atmosphere. The combined effect of irradiating the substrate with 193 nm laser radiation and the thermal activation in the hydrogen atmosphere decreases the cleaning time significantly. The hydrogen serves several purposes. Its presence in the reactor chamber prevents further oxidation of the substrate by gases desorbing from the reactor chamber walls, and aids in volatizing chemi/physisorbed contaminants on the wafer substrate surface. Since the substrate is largely fluorinated, the HF or atomic hydrogen H or atomic fluorine F produced at the surface can effectively etch regrown native oxide. Any trace oxygen in the reactor chamber is converted to ozone which can also react with other organic contamination, forming a volatile product which is pumped away. The resultant hydrogenated silicon surface is sufficiently contaminant free to accommodate homoepitaxial silicon deposition at 570.degree. C. as illustrated at equation (5), FIG. 2.
The deep uv laser radiation enhances the desorption of the contaminants via reactive photodesorption, laser induced thermal desorption and photochemical dry etching mechanisms, the sum of which produces the required pristine silicon surface. The deep uv laser radiation, 193 nm, 6.44 eV, is absorbed by the disilane, producing a population of metastable intermediates SiH.sub.z at or near the substrate surface. These intermediates can decompose at the hot silicon surface, or recombine to form various silane derivatives, or combine with hydrogen forming a volatile product. The products formed near the silicon surface can either decompose to form a film or be pumped away. The exact mechanism is not known, however the resulting film produced at 570.degree. C. is homoepitaxial. The intermediate products ultimately converted to the silicon film can gain enhanced adatom mobility through absorption of the uv radiation, increasing the probability that the atom finally resides at a preferred site for epitaxial growth. The laser enhances the desorption of hydrogen at the silicon surface, especially in the presence of the unstable disilane photodissociation products, effectively reducing undesired hydrogen entrapment as is produced in very low temperature amorphous hydrogenated silicon films. The 570.degree. C. substrate temperature provides sufficient thermal energy to decompose the intermediate responsible for silicon film growth, enhance silicon adatom mobility and enhance desorption of the reaction products.
It is recognized that various equivalents, alternatives and modifications are possible within the scope of the appended claims.