US20060150905A1 - Substrate processing apparatus - Google Patents

Substrate processing apparatus Download PDF

Info

Publication number
US20060150905A1
US20060150905A1 US10/530,527 US53052705A US2006150905A1 US 20060150905 A1 US20060150905 A1 US 20060150905A1 US 53052705 A US53052705 A US 53052705A US 2006150905 A1 US2006150905 A1 US 2006150905A1
Authority
US
United States
Prior art keywords
gas
substrate
reaction tube
supplied
film
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US10/530,527
Other languages
English (en)
Inventor
Masanori Sakai
Toru Kagaya
Nobuhito Shima
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kokusai Denki Electric Inc
Original Assignee
Hitachi Kokusai Electric Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hitachi Kokusai Electric Inc filed Critical Hitachi Kokusai Electric Inc
Assigned to HITACHI KOKUSAI ELECTRIC INC. reassignment HITACHI KOKUSAI ELECTRIC INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KAGAYA, TORU, SAKAI, MASANORI, SHIMA, NOBUHITO
Publication of US20060150905A1 publication Critical patent/US20060150905A1/en
Priority to US12/039,686 priority Critical patent/US7713582B2/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/455Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber

Definitions

  • the present invention relates to a substrate processing apparatus, and more particularly, to a substrate processing apparatus in which a gas supply structure for supplying gas which contributes to film formation is improved.
  • a substrate processing apparatus which carries out film forming processing using an ALD (Atomic Layer Deposition) method is known.
  • ALD atomic layer Deposition
  • two (or more) kinds of raw material gases used for forming a film are alternately supplied onto a substrate in a reaction chamber one kind by one kind, the gases adsorb on the substrate one atom layer by one atom layer, and a film is formed utilizing only surface reaction.
  • the gas supply amount of the raw material gas is controlled in flow rate by a mass flow controller (MFC) provided in a gas supply pipe.
  • MFC mass flow controller
  • the absorption amount is proportional to pressure ⁇ time.
  • L an amount corresponding to the pressure ⁇ time
  • L is constant and the pressure is higher, the same amount of gas can adsorb even if the time is shorter. That is, if the pressure in the reaction chamber is rapidly increased, the raw material gas can adsorb in a short time.
  • a gas supply pipe located downstream from the MFC is provide with a gas reservoir for storing raw material gas therein.
  • FIG. 6 shows an example in which a gas supply pipe is provided with a gas reservoir.
  • the gas supply pipe 51 is provided with first and second opening/closing valves 1 and 2 in front of and behind the gas reservoir 10 .
  • the first valve 1 located between an MFC 27 and the gas reservoir 10 is opened, the raw material gas is once stored in the gas reservoir 10 and then, the second valve 2 located between the gas reservoir 10 and the reaction tube 6 which is a reaction chamber is opened.
  • the pipe 51 and the opened second valve 2 between the gas reservoir 10 and the reaction tube 6 there also exist the MFC 27 and the long 51 and thus, conductance of the path becomes great, and the supply speed is increased. This will be explained using an expression.
  • Q supply speed (Pa ⁇ m 3 /sec)
  • C conductance (m 3 /sec)
  • P1 and P2 represent pressures (Pa) in front of and behind the pipe.
  • the supply speed is also increased, and the raw material gas can adsorb in a short time. That is, if the gas supply pipe is provided with the gas reservoir for storing the raw material gas, the supply speed of the raw material gas to be supplied into the reaction chamber can be increased. Thus, the raw material gas can absorb in a short time, and the film forming time can be shortened.
  • a plurality of kinds e.g., two kinds of reaction gases are alternately supplied onto a substrate one kind by one kind, the gases are allowed to adsorb on the substrate one atom layer by one atom layer, and a film is formed utilizing the surface reaction.
  • This step is defined as one cycle.
  • the thickness of the film is controlled by the number of cycles of the supply of the reaction gas. For example, when the film forming speed is defined as 1 ⁇ /cycle, in order to form a film of 500 ⁇ film, the processing is carried out by 500 cycles. That is, an extremely thin film is formed through one cycle, a predetermined cycles is repeated to obtain a desired thickness.
  • the raw material gas is once stored in the gas reservoir, and the raw material gas is supplied onto the substrate from the gas reservoir at higher supply speed. For example, if one kind of raw material gas is supplied onto the substrate from a supply port of that raw material gas along a radial direction of the substrate, a film thickness of the substrate closer to the supply port of the raw material gas becomes thick, the thickness of the film is locally increased, and there is an adverse possibility that only one location of the periphery is convexed. In the next cycle, if the gases are supplied at higher supply speed from the gas reservoir using the gas reservoir, a film is formed on a portion of the substrate other than the locally thick portion (convexed portion).
  • the locally thickened portion is dispersed, and the film thickness is equalized.
  • the number of cycles is less than 60, the dispersion of the locally thickened portion is inferior, i.e., the film forming operation is finished before the locally thickened portion is dispersed, and the periphery becomes uneven and the consistency of the film thickness is deteriorated in some cases.
  • it is a main object of the present invention is to provide a substrate processing apparatus capable of achieving excellent consistency of film thickness when a thin film is formed.
  • a substrate processing apparatus comprising: a reaction chamber forming a space in which a substrate is to be processed, a gas supply pipe which is connected to said reaction chamber and which supplies processing gas for said substrate, and a gas exhaust pipe for exhausting an inside of said reaction chamber, wherein
  • a gas reservoir for storing gas to be supplied to said reaction chamber and a bypass line which bypasses said gas reservoir are juxtaposed to each other in a portion of said gas supply pipe, and
  • said substrate processing apparatus further comprises a control unit which allows the processing gas to be supplied to said reaction chamber using one of said gas reservoir and said bypass line when said substrate is processed.
  • the processing gas is supplied to the reaction chamber using the bypass line without using the gas reservoir, the processing gas is not abruptly supplied to the reaction chamber, the gas is sufficiently dispersed and thus, the consistency of film thickness becomes excellent. Therefore, if the bypass line is used when a thin film is formed, a film having equalized or constant thickness can be formed even if its thickness is thin.
  • FIG. 1 is a schematic traverse sectional view showing one example of a reaction tube of a substrate processing apparatus according to the present invention.
  • FIG. 2 is a schematic vertical sectional view showing the example of the reaction tube of the substrate processing apparatus of the invention.
  • FIGS. 3A and 3B are perspective view showing one example of a nozzle and gas holes of a second buffer chamber.
  • FIG. 4 show a relation between a substrate and a supply position of gas.
  • FIGS. 5A and 5B show a state of a substrate, wherein FIG. 5A is a plan view and FIG. 5B is a side view.
  • FIG. 6 is a schematic transverse sectional view showing one example of a reaction tube of a previously proposed substrate processing apparatus.
  • FIGS. 1 and 2 show one example of a vertical substrate processing apparatus according to the embodiment.
  • a basic structure of the vertical substrate processing apparatus will be explained using FIGS. 1 and 2 .
  • structures of a gas reservoir 10 and a bypass pipe 11 which are added to a basic structure are omitted.
  • a quartz reaction tube 6 is provided inside of a heater 31 .
  • the reaction tube 6 constitutes a reaction chamber which processes wafers (substrates) 7 to be processed.
  • a diameter of the substrate 7 is 200 mm.
  • a lower end opening of the reaction tube 6 is air-tightly closed with a seal cap 35 .
  • a boat 39 is provided in a standing attitude above the seal cap 35 and is inserted into the reaction tube 6 .
  • the boat 39 is connected to a rotation mechanism 20 through a rotation shaft 19 which is rotatably supported by a bearing 18 .
  • the boat 39 (substrates 7 ) is arranged such that the boat 39 can rotate.
  • the plurality of substrates 7 to be batch-processed are placed in the boat 39 in a multi-stacked manner in their horizontal postures in an axial direction of the reaction tube 6 .
  • the heater 31 heats the substrates 7 in the reaction tube 6 to a predetermined temperature.
  • the gas supply pipes function as supply paths for supplying a plurality of kinds of gases (here, two kinds of gases).
  • the first gas supply pipe 51 is connected to one side of the reaction tube 6 without through a remote plasma unit.
  • the second gas supply pipe 52 is connected to the one side of the reaction tube 6 through a remote plasma unit 37 .
  • there are two kinds of gases are supplied to the substrates 7 in the reaction tube 6 , i.e., gas which is not excited with plasma and is supplied, and gas which is excited with plasma and is supplied as active species.
  • the first supply pipe 51 and the second supply pipe 52 are respectively provided with MFCs 27 and 28 so that flow rates of gases flowing into the first supply pipe 51 and the second supply pipe 52 are controlled.
  • a gas exhaust pipe 40 as an exhaust path for exhausting gas from the reaction tube 6 is connected to the other side of the reaction tube 6 .
  • a vacuum pump as vacuum exhaust means (not shown) is connected to the gas exhaust pipe 40 .
  • a remote plasma unit 37 is connected to a nozzle 43 which stands in a second buffer chamber 41 in the reaction tube 6 along the boat 39 .
  • the second buffer chamber 41 is formed in an arc shape in a space between an inner wall of the reaction tube 6 and the substrate 7 along the inner wall of the reaction tube 6 in the illustrated example.
  • the second buffer chamber 41 extends along the inner wall of the reaction tube 6 and provided along the stacking direction of the substrates 7 from a lower portion to an upper portion of the inner wall of the reaction tube 6 .
  • An end of a wall of the second buffer chamber 41 which is adjacent to the substrate 7 is provided with second buffer chamber holes 46 as gas supply ports.
  • the second buffer chamber holes 46 open toward a center of the reaction tube 6 (substrates 7 ).
  • a nozzle 43 connected to the remote plasma unit 37 is disposed is disposed in the second buffer chamber 41 on an end of the second buffer chamber 41 opposite from the end provided with the second buffer chamber holes 46 .
  • the nozzle 43 extends along the stacking direction of the substrate 7 from the lower portion to the upper portion of the reaction tube 6 .
  • the nozzle 43 is provided with a plurality of nozzle holes 47 .
  • the nozzle 43 and the second buffer chamber 41 are respectively provided with the nozzle holes 47 and the second buffer chamber holes 46 .
  • the opening states of the holes will be explained using FIGS. 3A and 3B .
  • FIG. 3A is a perspective view of the nozzle shown in FIG. 1 .
  • FIG. 3B is a perspective view of the second buffer chamber 41 shown in FIG. 1 also.
  • the nozzle 43 shown in FIG. 3A is a pipe having a circular cross section.
  • the nozzle holes 47 are straightly formed in a side surface of the nozzle 43 from a substantially uppermost portion of the nozzle 43 to a location corresponding to a bottom of the second buffer chamber 41 such that the nozzle holes 47 are arranged from an upstream side toward a downstream side of gas flow. Opening areas of the nozzle holes 47 are formed such that the opening areas are increased from the upstream side (downward in FIGS. 3A and 3B ) as viewed from the second supply pipe 52 toward the downstream side (upward in FIGS. 3A and 3B ), the conductance is varied so that gas can issue equally in any of upstream side and downstream side.
  • the second buffer chamber 41 shown in FIG. 3B is a pipe having an arc cross section.
  • the second buffer chamber holes 46 having the same opening areas are formed in an end of an inner curved surface of the second buffer chamber 41 such that the second buffer chamber holes 46 are straightly arranged in the stacking direction of the substrates 7 .
  • the inner wall of the reaction tube 6 is provided with a first buffer chamber 42 which is adjacent to the second buffer chamber 41 .
  • a first supply pipe 51 is connected to a lower portion of the first buffer chamber 42 .
  • the first buffer chamber 42 also has first buffer chamber holes 48 formed at the same pitch at locations adjacent to the substrates 7 .
  • the first buffer chamber 42 is provided at its lower portion with a reaction gas introducing port.
  • the first buffer chamber holes 48 are formed such that opening areas thereof are increased from the upstream side toward the downstream side so that gas can issue equally in any of upstream side and downstream side.
  • control unit 60 which controls a flowing manner of two kinds of gases and controls film forming temperature of the substrate 7 .
  • the control unit 60 has a gas supply control function for controlling such as to allow the two kinds of gases to flow alternately one kind by one kind.
  • the control unit 60 also has a temperature control function for controlling film forming temperature by heating using a heater.
  • the reaction gas is DCS (SiH 2 Cl 2 : dichlorsilane), and NH 3 active species activated with plasma.
  • substrates 7 on which films are to be formed are mounted on the boat 39 and brought into the reaction tube 6 (also simply called furnace, hereinafter). Then, Si 3 N 4 films are formed.
  • the temperature in the reaction tube 6 at that time is set to such a value that a film having excellent adhesion with respect to the ground film and little defect of interface is formed, e.g., 350 to 600° C.
  • the ALD method in which NH 3 and DCS are alternately allowed to flow to form a film one atom layer by one atom layer is used.
  • NH 3 is supplied from the second supply pipe 52 . Since the NH 3 has higher reaction temperature than that of the DCS, NH 3 does not react at the temperature in the reaction tube 6 . Thus, the NH 3 is excited with plasma using the remote plasma unit 37 to activate the same and NH 3 is allowed to flow as active species so that the NH 3 reacts even at the temperature in the reaction tube 6 . At that time, the pressure in the reaction tube 6 is maintained at relatively low pressure of 40 to 60 Pa, the NH 3 excited with plasma and brought into the active species is supplied for 5 to 120 seconds. Here, gas flowing into the reaction tube 6 is only NH 3 which was excited with plasma and brought into active species, and no DCS exists. Thus, NH 3 which was excited with plasma and brought into active species does not vapor phase reacts, and adsorbs on the ground film on the substrate 7 .
  • the nozzle holes 47 formed in the nozzle 43 is formed such that their opening areas are gradually increased from the upstream side toward the downstream side of the gas flow so that the flow rate of NH 3 issuing into the second buffer chamber 41 is equalized.
  • the flow speed of NH 3 passing through the nozzle holes 47 and issuing into the second buffer chamber 41 is high on the upstream side and low on the downstream side, but the flow rates are all the same between all of the nozzle holes 47 .
  • the NH 3 issuing into the second buffer chamber 41 is once introduced there, and the pressure in the second buffer chamber 41 is equalized.
  • the second buffer chamber holes 46 are provided such that each of the holes is located at a location corresponding to a middle of a distance between substrates 7 which are placed in the multi-stacked manner.
  • NH 3 which is processing gas is sufficiently supplied to each of the stacked substrates 7 .
  • DCS is supplied from the first supply pipe 51 . Since the DCS reacts at the temperature in the reaction tube 6 , it is unnecessary to excite with plasma using the remote plasma unit 37 .
  • the pressure in the reaction tube 6 at that time is increased to 266 to 931 Pa which is higher than that when NH 3 is supplied. If DCS is supplied, NH 3 on the ground film and DCS surface reacts with each other and the Si 3 N 4 film is formed.
  • the first buffer chamber 42 is formed with the first buffer chamber holes 48 whose opening areas are gradually increased from the upstream side toward the downstream side of gas flow.
  • the first buffer chamber holes 48 is provided toward the center of the reaction tube 6 (substrates 7 ). As a result, flow rate of DCS supplied from the first buffer chamber holes 48 toward the substrates 7 is the same although the flow speed is different, and the DCS issues into the reaction tube 6 .
  • one more set of the nozzle 43 and the second buffer chamber 41 which are the same as those used for supplying NH 3 is disposed in the reaction tube 6 instead of the first buffer chamber 42 , and DCS is supplied from the second buffer chamber holes 46 because both the flow rate and flow speed can be equalized.
  • the step for alternately flowing NH 3 and DCS is defined as one cycle.
  • An Si 3 N 4 film having predetermined thickness is formed by repeating this cycle.
  • the ALD method since two kinds of gases which contribute to the film formation do not exist in the vapor phase at a time, gas adsorbs the ground surface and reacts with the ground film. Therefore, a film having excellent with respect to the ground film can be obtained, and defect in interface is reduced as compared with the CVD (Chemical Vapor Deposition) method in which two kinds of gases are allowed to flow at a time.
  • CVD Chemical Vapor Deposition
  • NH 3 which is required to be excited with plasma is excited with plasma and brought into the active species and allowed to flow. Therefore, a film can be formed at the reaction temperature by means of DCS gas which need not be excited with plasma and thus, the film can be formed at temperature as low as 350 to 600° C.
  • the gas reservoir 10 for storing gas is provided downstream (between the MFC 27 and the reaction tube 6 ) from the MFC 27 of the first supply pipe 51 .
  • the gas reservoir 10 comprises a gas tank or a spiral pipe having greater gas capacity than a normal pipe for example.
  • a bypass pipe 11 is connected to the first supply pipe 51 downstream from the MFC 27 .
  • the bypass pipe 11 bypasses the gas reservoir 10 .
  • the first supply pipe 51 is provided at its upstream side in the vicinity of the gas reservoir 10 with a first valve 1 which opens and closes a pipe path, and at its downstream with a second valve 2 which opens and closes the pipe path.
  • the bypass pipe 11 is provided with a third valve 3 which opens and closes a pipe path.
  • the second supply pipe 52 is provided at its upstream side in the vicinity of the remote plasma unit 37 with a fourth valve 4 which opens and closes a pipe path so that if the fourth valve 4 is opened and closed, NH 3 gas as second kind of gas can be supplied to the reaction tube 6 or the supply of the gas can be stopped.
  • the gas exhaust pipe 40 is provided with an exhaust valve (not shown) which adjusts the opening and closing operations and an opening degree of the pipe path. Gas can be exhausted from the reaction tube 6 or the exhausting operation can be stopped by opening and closing the exhaust valve. Gas can be exhausted from the reaction tube 6 while maintaining predetermined pressure in the reaction tube 6 by adjusting the opening degree of the exhaust valve.
  • the exhaust valve may be a single valve having a function for opening and closing and a function for adjusting the opening degree, or may comprise a plurality of valves including a valve having the opening and closing function and a valve having the opening degree-adjusting function.
  • control unit 60 which controls the first, second, third and fourth valves 1 , 2 , 3 and 4 , as well as the heater 31 .
  • the control unit 60 controls the exhaust valve and the first, second and third valves 1 , 2 and 3 to allow DCS gas to flow into the first supply pipe 51 and store the gas in the gas reservoir 10 , and DCS gas stored in the gas reservoir 10 is supplied to the reaction tube 6 or DCS gas is supplied to the reaction tube 6 through the bypass pipe 11 without using the gas reservoir 10 in a state in which exhaust operation of the reaction tube 6 is stopped or the exhaust operation is carried out. With this, the pressure in the reaction tube 6 is increased and the substrate 7 is exposed to DCS gas. Further, by supplying NH 3 gas into the reaction tube 6 from the second supply pipe 52 through the remote plasma unit 37 while exhausting gas from the reaction tube 6 , the substrate 7 is exposed to active species obtained by exciting NH 3 gas with plasma.
  • a gas supply pipe 52 (line) for NH 3 does not have the gas reservoir 10 , and DCS is supplied using a gas supply pipe 51 (line) having the gas reservoir 10 .
  • the raw material gas is first allowed to flow into the reaction tube 6 using a pipe having no gas reservoir 10 in the following example, a method n which raw material gas is first are allowed to flow using a pipe having the gas reservoir 10 can also be employed similarly.
  • a substrate 7 on which a film is to be formed is mounted in the boat 39 and transferred into the reaction tube 6 .
  • the following operations (1) to (4) are defined as one cycle, and this cycle is repeatedly carried out.
  • NH 3 gas which need to be excited with plasma and DCS gas which need not be excited with plasma are allowed to flow together.
  • the fourth valve 4 provided in the second supply pipe 52 and the exhaust valve provided in the gas exhaust pipe 40 are both opened, NH 3 is excited with plasma by the remote plasma unit 37 and brought into active species and passes through the second buffer chamber 41 from the second supply pipe 52 , NH 3 is supplied to the substrates 7 from the second buffer chamber holes 46 formed for respective substrates 7 and arrange at the same distances from one another as distances between the substrates 7 provided in the second buffer chamber 41 and in this state, NH 3 is exhausted from the gas exhaust pipe 40 .
  • the exhausting operation from the gas exhaust pipe 40 is appropriately adjusted and the pressure in the reaction tube 6 is set to 10 to 100 Pa.
  • a supply flow rate of NH 3 to be controlled by the MFC 28 is in a range of 100 to 10000 sccm.
  • Time during which the substrate 7 is exposed to the active species obtained by exciting NH 3 with plasma is 2 to 60 seconds.
  • the temperature in the reaction tube 6 is set to 300 to 600° C. Since the reaction temperature of NH 3 is high, NH 3 does not react at the temperature in the reaction tube 6 , but since NH 3 is excited with plasma and brought into active species and then is allowed to flow, NH 3 can react even if the temperature in the reaction tube 6 is maintained in the preset low temperature range.
  • the first valve 1 on the upstream side of the first supply pipe 51 is opened, the second valve 2 on the downstream side is closed, and DCS is also allowed to flow.
  • DCS is supplied to the gas reservoir 10 provided between the valves 1 and 2 and a predetermined amount of DCS is stored in the gas reservoir 10 under the predetermined pressure
  • the first valve 1 is also closed to confine DCS in the gas reservoir 10 .
  • DCS is stored in the gas reservoir 10 such that the pressure therein becomes 20000 Pa or higher.
  • a pipe system is constituted such that conductance between the gas reservoir 10 and the reaction tube 6 becomes 1. 5 ⁇ 10 ⁇ 3 m 3 /s or higher.
  • the gas reservoir capacity is in a range of 100 to 300 cc when the reaction tube capacity is 1001 (100 liters), and the gas reservoir 10 has capacity of 1/1000 to 3/1000 times of the reaction tube capacity as a capacity ratio.
  • Gas flowing into the reaction tube 6 is active species obtained by exciting NH 3 with plasma, and there exists no DCS.
  • NH 3 does not vapor phase reacts, and NH 3 which was excited with plasma and brought into active species adsorbs to the ground film on the substrate 7 .
  • NH 3 supplied from the nozzle 43 to the second buffer chamber 41 is supplied to the substrates 7 from the second buffer chamber holes 46 which are formed for respective substrates 7 and arrange at the same distances from one another as distances between the substrates 7 .
  • the fourth valve 4 is closed to stop the flow of NH 3 into the reaction tube 6 .
  • the second valve 2 located downstream from the gas reservoir 10 is opened.
  • DCS stored in the gas reservoir 10 supplied at a dash to the substrates 7 from the first buffer holes 48 which are formed for respective substrates 7 and arrange at the same distances from one another as distances between the substrates 7 through the first buffer chamber 42 .
  • the adjusting means of the pressure in the reaction tube 6 sets such that the pressure is increased so that the partial pressure of DCS is increased to promote the reaction with the NH 3 .
  • the pressure in the reaction tube 6 is abruptly increased by the supply of DCS to about 266 to 931 Pa which is higher that of the case of NH 3 .
  • the supply flow rate of DCS is 100 to 2000 cc. Time during which DCS was supplied is set to 2 to 4 seconds, time during which the substrate was exposed to the increased pressure atmosphere is set to 2 to 4 seconds, and the total time was set to 6 seconds.
  • the temperature in the reaction tube 6 is the same as that when NH 3 is supplied, and is 300 to 600° C. NH 3 on the ground film and DCS are reacted with each other by supplying DCS, and an Si 3 N 4 film is formed on the substrate 7 .
  • the second valve 2 is closed to stop the supply of DCS from the gas reservoir 10 . After the second valve 2 is closed, time elapsed until the next supply starts can be used as DCS storing time (that is, it is unnecessary to spend time wastefully only for storing time action while another operation is being carried out, and the first valve 1 is opened to star the supply of DCS to the gas reservoir 10 ).
  • the boat 39 on which the substrates 7 are placed is rotated at a constant speed.
  • the rotation speed of the substrate 7 is about 14 to 30 seconds in the one cycle, but it is preferable that the rotation speed is set to about 10 seconds in terms of throughput.
  • the position of the substrate 7 is the same every time when raw material gas, e.g. DCS is supplied. That is, the substrate 7 is rotated but when DCS is supplied from the first buffer chamber holes 48 , gas is supplied from one peripheral edge of the substrate 7 toward the substrate 7 . If gas is supplied in this manner, since the gas reservoir 10 is used, the supply speed of gas is fast. Therefore, as shown in FIGS. 5A and 5B , there is a tendency that an end 65 of the substrate closer to the first buffer chamber holes 48 (gas supply ports) having narrow width is thickened in film thickness.
  • raw material gas e.g. DCS is supplied. That is, the substrate 7 is rotated but when DCS is supplied from the first buffer chamber holes 48 , gas is supplied from one peripheral edge of the substrate 7 toward the substrate 7 . If gas is supplied in this manner, since the gas reservoir 10 is used, the supply speed of gas is fast. Therefore, as shown in FIGS. 5A and 5B , there is a tendency that an end 65 of the substrate closer to the first buffer chamber
  • the rotation speed and gas supply timing are finely adjusted so that the same positions of the substrates 7 are not located closer to the first buffer chamber holes 48 .
  • this fine adjustment is carried out in such a manner that the rotation speed is increased or decreased such that gas is supplied so that the gas supply position P is deviated through 45° each cycle, or the rotation speed is set constant and the gas supply timing is staggered.
  • This fine adjustment is effective when a thick film requiring alternative supply of 60 cycles or more is to be formed, but when a thin film of less than 60 cycles is to be formed, although it is possible to avoid the case in which only one portion of the substrate 7 is not opposed to the first buffer chamber hole 48 depending upon the combination of the rotation speed and the gas supply timing, since the rotation number is small, there is an adverse possibility that the degree of dispersion is low and the periphery becomes uneven. As the rotation number is smaller, i.e., as the film thickness formed on the substrate is thinner, the possibility of deterioration of consistency due to unevenness becomes higher.
  • the films are divided into thick films and thin films on the basis of 60 cycles, but this numerical value is only an example and the invention is not limited to this.
  • a film of about 1 ⁇ thickness when a film of about 1 ⁇ thickness is formed in one cycle, the thickness becomes 60 ⁇ in 60 cycles.
  • a film of 100 ⁇ or less thickness is called a thin film, and a film of 1000 ⁇ or more is called a thick film.
  • DCS raw material gas
  • the bypass pipe 11 When a film of less than 60 cycles is to be formed, raw material gas, in this embodiment DCS is supplied using the bypass pipe 11 without using the gas reservoir 10 . If DCS is supplied using the bypass pipe 11 , the gas supply speed to the substrate 7 is as slow as 1 ⁇ 5 of a case in which gas is supplied using the gas reservoir 10 . Since gas is supplied while taking relatively long time, gas is dispersed, gas is not concentrated on only a narrow portion of the rotating substrate 7 , and gas is dispersed in a wide range. Thus, the adverse possibility of unevenness is eliminated, and even when a thin film is to be formed, the consistency within a surface of the substrate 7 can be enhanced.
  • the bypass pipe 11 capable of supplying gas to the reaction tube 6 through the mass flow controller 27 for desired time is provided.
  • the bypass pipe 11 is used, and when a film having greater thickness than 60 ⁇ is to be formed, the gas reservoir 10 is used. If the supply paths are properly selected, it is possible to form having excellent consistency of thickness in both thin and thick films.
  • the first and second valves 1 and 2 are kept opened without using the gas reservoir 10 as a tank, and the gas reservoir 10 is used as a path of gas, i.e., as a pipe.
  • a film was formed using the gas reservoir 10 as a pipe, the consistency of film thickness and film thickness reproducibility were inferior as compared with a case in which the bypass pipe 11 was used. It is believed that this is because gas is accumulated in the gas reservoir 10 , stagnation is generated and this can not be removed even by the subsequent exhausting operation, and the gas vapor phase reacted with subsequent gas. This deterioration was overcome by sufficiently increasing the exhausting operation time after the gas supply. However, this is not preferable because the exhausting operation time is increased in addition to the additional supply time of several seconds per one cycle, and the film forming time is increased. Thus, it is effective to provide the bypass pipe 11 .
  • one gas tank or one spiral pipe is provided as the gas reservoir 10 .
  • the present invention is not limited to this, and a plurality of gas reservoirs may be provided juxtaposed to one another.
  • the gas reservoir 10 of this invention is not limited to the gas tank or spiral pipe, and the gas reservoir may be any means only if it can store gas and discharge gas at a dash.
  • the gas supply pipe of DCS may be thicker than a normal pipe and the MFC capacity may be increased correspondingly.
  • the number of the gas supply pipes may be two or more. In this case, the number of cylinders which function as DCS supply sources may be increased in accordance with the number of gas supply pipes. Further, since the vapor pressure of DCS is low, the cylinder may be heated to increase the amount of vaporization of DCS. Further, DCS may forcibly be sent into the reaction tube 6 by a pump.
  • the present invention is applied to the vertical substrate processing apparatus in this embodiment, but the invention can also be applied to a producing method of a semiconductor device.
  • gas is exhausted from the reaction chamber (reaction tube), processing gas is supplied to the reaction chamber, and a substrate in the reaction chamber is processed.
  • the processing gas is stored in a portion of a supply path through which the processing gas flows, the processing gas stored in the portion of the supply path is supplied to the reaction chamber, or the processing gas is supplied to the reaction chamber without storing the processing gas in the portion of the supply path, and a film is formed on the substrate.
  • the processing gas is supplied to the reaction chamber at a normal supply speed without storing the processing gas in the portion of the supply path and the processing gas can sufficiently be dispersed over the substrate and thus, the thickness of the formed film is equalized within its surface.
  • gas is supplied to the reaction chamber without storing the gas, a film having the constant thickness can be formed even if its thickness is thin.
  • DCS and NH 3 requiring the remote plasma unit are used as reaction gases in the above embodiment, the present invention is not limited to this, and gas which does not require the remote plasma unit can also be used.
  • gas which does not require the remote plasma unit can also be used.
  • gas reservoirs can be used for both the gas supply pipes and thus, a bypass line is also provided for each of them.
  • Al 2 O 3 film is to be used using Al(CH 3 ) 3 and ozone O 3
  • Al(CH 3 ) 3 is stored in the gas reservoir and O 3 is supplied from an ozone generator.
  • gas is supplied using the bypass line disposed juxtaposed to the gas reservoir, even a thin film has excellent thickness consistency, and a film having excellent consistency can be obtained irrespective of its thickness.
  • the present invention can preferably be utilized for a substrate film-forming apparatus using the ALD method.

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Vapour Deposition (AREA)
US10/530,527 2002-10-08 2003-10-06 Substrate processing apparatus Abandoned US20060150905A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/039,686 US7713582B2 (en) 2002-10-08 2008-02-28 Substrate processing method for film formation

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2002295323A JP4204840B2 (ja) 2002-10-08 2002-10-08 基板処埋装置
JP2002295323 2002-10-08
PCT/JP2003/012786 WO2004034454A1 (ja) 2002-10-08 2003-10-06 基板処理装置

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US12/039,686 Division US7713582B2 (en) 2002-10-08 2008-02-28 Substrate processing method for film formation

Publications (1)

Publication Number Publication Date
US20060150905A1 true US20060150905A1 (en) 2006-07-13

Family

ID=32089209

Family Applications (2)

Application Number Title Priority Date Filing Date
US10/530,527 Abandoned US20060150905A1 (en) 2002-10-08 2003-10-06 Substrate processing apparatus
US12/039,686 Active 2026-01-28 US7713582B2 (en) 2002-10-08 2008-02-28 Substrate processing method for film formation

Family Applications After (1)

Application Number Title Priority Date Filing Date
US12/039,686 Active 2026-01-28 US7713582B2 (en) 2002-10-08 2008-02-28 Substrate processing method for film formation

Country Status (4)

Country Link
US (2) US20060150905A1 (enrdf_load_stackoverflow)
JP (1) JP4204840B2 (enrdf_load_stackoverflow)
TW (1) TWI232518B (enrdf_load_stackoverflow)
WO (1) WO2004034454A1 (enrdf_load_stackoverflow)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080213479A1 (en) * 2007-02-16 2008-09-04 Tokyo Electron Limited SiCN film formation method and apparatus
US20100035440A1 (en) * 2008-08-06 2010-02-11 Hitachi-Kokusai Electric, Inc. Substrate processing apparatus and method of manufacturing semiconductor device
US20100136260A1 (en) * 2008-10-04 2010-06-03 Tokyo Electron Limited Film formation method in vertical batch cvd apparatus
US20120315394A1 (en) * 2010-03-19 2012-12-13 Tokyo Electron Limited Film forming apparatus, film forming method, method for optimizing rotational speed, and storage medium
US20140213069A1 (en) * 2013-01-30 2014-07-31 Hitachi Kokusai Electric Inc. Substrate Processing Apparatus, Method of Manufacturing Semiconductor Device and Non-transitory Computer-readable Recording Medium
US20150170909A1 (en) * 2013-12-17 2015-06-18 Hitachi Kokusai Electric Inc. Method of manufacturing semiconductor device and non-transitory computer-readable recording medium
US9136148B2 (en) 2010-05-20 2015-09-15 Tokyo Electron Limited Substrate processing apparatus, control device thereof, and control method thereof
US20160189951A1 (en) * 2014-12-30 2016-06-30 Samsung Electronics Co., Ltd. Methods of forming a layer and methods of manufacturing a semiconductor device using the same
US10811271B2 (en) 2014-09-30 2020-10-20 Kokusai Electric Corporation Substrate processing device, manufacturing method for semiconductor device, and reaction tube
US11453942B2 (en) * 2017-02-23 2022-09-27 Kokusai Electric Corporation Substrate processing apparatus and method of manufacturing semiconductor device
US11542601B2 (en) * 2016-02-09 2023-01-03 Hitachi Kokusai Electric Inc. Substrate processing apparatus and method of manufacturing semiconductor device

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005015619A1 (ja) * 2003-08-07 2005-02-17 Hitachi Kokusai Electric Inc. 基板処理装置および半導体装置の製造方法
US7740704B2 (en) * 2004-06-25 2010-06-22 Tokyo Electron Limited High rate atomic layer deposition apparatus and method of using
KR100871003B1 (ko) * 2004-08-06 2008-11-27 도쿄엘렉트론가부시키가이샤 박막 형성 방법 및 박막 형성 장치
JP4718141B2 (ja) * 2004-08-06 2011-07-06 東京エレクトロン株式会社 薄膜形成方法及び薄膜形成装置
JP4506677B2 (ja) * 2005-03-11 2010-07-21 東京エレクトロン株式会社 成膜方法、成膜装置及び記憶媒体
US8202367B2 (en) 2006-03-30 2012-06-19 Mitsui Engineering & Shipbuilding Co., Ltd. Atomic layer growing apparatus
JP4461441B2 (ja) 2006-08-07 2010-05-12 エルピーダメモリ株式会社 半導体装置の製造方法
JP5235293B2 (ja) * 2006-10-02 2013-07-10 東京エレクトロン株式会社 処理ガス供給機構および処理ガス供給方法ならびにガス処理装置
JP2010084156A (ja) * 2008-09-29 2010-04-15 Tokyo Electron Ltd 処理ガス供給系及び成膜装置
JP5325759B2 (ja) * 2009-12-21 2013-10-23 ラムバス・インコーポレーテッド 半導体装置の製造方法
JP2010206218A (ja) * 2010-06-07 2010-09-16 Hitachi Kokusai Electric Inc シリコン酸化膜の形成方法
JP5920242B2 (ja) 2012-06-02 2016-05-18 東京エレクトロン株式会社 成膜方法及び成膜装置
DE102013020662A1 (de) 2013-12-06 2015-06-11 Kienle + Spiess Gmbh Verfahren zur Herstellung von Lamellen für ein Lamellenpaket, insbesondere für elektrische Maschinen und Generatoren,Vorrichtung mit wenigstens einer Stanzpresse sowie nach dem Verfahren hergestellte Lamelle und Lamellenpaket.
CN115513101B (zh) * 2022-11-15 2023-01-24 深圳仕上电子科技有限公司 一种等离子蚀刻清洗工艺

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6182603B1 (en) * 1998-07-13 2001-02-06 Applied Komatsu Technology, Inc. Surface-treated shower head for use in a substrate processing chamber
US6231672B1 (en) * 1998-05-18 2001-05-15 Ips Ltd. Apparatus for depositing thin films on semiconductor wafer by continuous gas injection
US6328864B1 (en) * 1997-04-30 2001-12-11 Tokyo Electron Limited Vacuum processing apparatus
US20020033229A1 (en) * 2000-09-19 2002-03-21 Lebouitz Kyle S. Apparatus for etching semiconductor samples and a source for providing a gas by sublimination thereto
US6605134B2 (en) * 2000-09-22 2003-08-12 Nippon Sanso Corporation Method and apparatus for collecting rare gas

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62106627A (ja) * 1985-11-05 1987-05-18 Hitachi Ltd 半導体製造装置
JPH01296613A (ja) * 1988-05-25 1989-11-30 Nec Corp 3−v族化合物半導体の気相成長方法
JPH02199820A (ja) * 1989-01-30 1990-08-08 Fujitsu Ltd 気相処理装置
JP3126787B2 (ja) * 1992-01-30 2001-01-22 理化学研究所 成膜方法および成膜装置
JPH0645256A (ja) * 1992-07-21 1994-02-18 Rikagaku Kenkyusho ガスパルスの供給方法およびこれを用いた成膜方法
JPH07176519A (ja) * 1993-12-17 1995-07-14 Shibaura Eng Works Co Ltd 放電処理装置
JPH07325279A (ja) 1994-06-01 1995-12-12 Dainippon Screen Mfg Co Ltd 減圧処理装置及び方法
US5955037A (en) * 1996-12-31 1999-09-21 Atmi Ecosys Corporation Effluent gas stream treatment system having utility for oxidation treatment of semiconductor manufacturing effluent gases
US6174377B1 (en) * 1997-03-03 2001-01-16 Genus, Inc. Processing chamber for atomic layer deposition processes
JP3529989B2 (ja) * 1997-09-12 2004-05-24 株式会社東芝 成膜方法及び半導体装置の製造方法
TW576873B (en) * 2000-04-14 2004-02-21 Asm Int Method of growing a thin film onto a substrate
US20020195056A1 (en) * 2000-05-12 2002-12-26 Gurtej Sandhu Versatile atomic layer deposition apparatus
KR100332313B1 (ko) * 2000-06-24 2002-04-12 서성기 Ald 박막증착장치 및 증착방법
US6905547B1 (en) * 2000-12-21 2005-06-14 Genus, Inc. Method and apparatus for flexible atomic layer deposition
JP4490008B2 (ja) * 2001-08-31 2010-06-23 株式会社アルバック 真空処理装置及び真空処理方法
US6656282B2 (en) * 2001-10-11 2003-12-02 Moohan Co., Ltd. Atomic layer deposition apparatus and process using remote plasma
US20030123216A1 (en) * 2001-12-27 2003-07-03 Yoon Hyungsuk A. Deposition of tungsten for the formation of conformal tungsten silicide
JP2003218106A (ja) * 2002-01-23 2003-07-31 Hitachi Kokusai Electric Inc 半導体装置の製造方法
JP3957549B2 (ja) * 2002-04-05 2007-08-15 株式会社日立国際電気 基板処埋装置
KR100439948B1 (ko) * 2002-04-19 2004-07-12 주식회사 아이피에스 리모트 플라즈마 ald 장치 및 이를 이용한 ald 박막증착방법
US6915592B2 (en) * 2002-07-29 2005-07-12 Applied Materials, Inc. Method and apparatus for generating gas to a processing chamber
US6936086B2 (en) * 2002-09-11 2005-08-30 Planar Systems, Inc. High conductivity particle filter
US7927658B2 (en) * 2002-10-31 2011-04-19 Praxair Technology, Inc. Deposition processes using group 8 (VIII) metallocene precursors
KR100498467B1 (ko) * 2002-12-05 2005-07-01 삼성전자주식회사 배기 경로에서의 파우더 생성을 방지할 수 있는 원자층증착 장비
US7335396B2 (en) * 2003-04-24 2008-02-26 Micron Technology, Inc. Methods for controlling mass flow rates and pressures in passageways coupled to reaction chambers and systems for depositing material onto microfeature workpieces in reaction chambers
US20050022735A1 (en) * 2003-07-31 2005-02-03 General Electric Company Delivery system for PECVD powered electrode
JP5264039B2 (ja) * 2004-08-10 2013-08-14 東京エレクトロン株式会社 薄膜形成装置及び薄膜形成方法
US7485338B2 (en) * 2005-03-31 2009-02-03 Tokyo Electron Limited Method for precursor delivery

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6328864B1 (en) * 1997-04-30 2001-12-11 Tokyo Electron Limited Vacuum processing apparatus
US6231672B1 (en) * 1998-05-18 2001-05-15 Ips Ltd. Apparatus for depositing thin films on semiconductor wafer by continuous gas injection
US6182603B1 (en) * 1998-07-13 2001-02-06 Applied Komatsu Technology, Inc. Surface-treated shower head for use in a substrate processing chamber
US20020033229A1 (en) * 2000-09-19 2002-03-21 Lebouitz Kyle S. Apparatus for etching semiconductor samples and a source for providing a gas by sublimination thereto
US6605134B2 (en) * 2000-09-22 2003-08-12 Nippon Sanso Corporation Method and apparatus for collecting rare gas

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8591989B2 (en) 2007-02-16 2013-11-26 Tokyo Electron Limited SiCN film formation method and apparatus
US20080213479A1 (en) * 2007-02-16 2008-09-04 Tokyo Electron Limited SiCN film formation method and apparatus
US10290494B2 (en) 2008-08-06 2019-05-14 Kokusai Electric Corporation Method of manufacturing semiconductor device and method of processing substrate
US20100035440A1 (en) * 2008-08-06 2010-02-11 Hitachi-Kokusai Electric, Inc. Substrate processing apparatus and method of manufacturing semiconductor device
US20100136260A1 (en) * 2008-10-04 2010-06-03 Tokyo Electron Limited Film formation method in vertical batch cvd apparatus
US8257789B2 (en) * 2008-10-04 2012-09-04 Tokyo Electron Limited Film formation method in vertical batch CVD apparatus
KR101287725B1 (ko) * 2008-10-04 2013-07-19 도쿄엘렉트론가부시키가이샤 종형 뱃치 cvd 장치, 종형 뱃치 cvd 장치에 있어서의 성막 방법 및 컴퓨터로 판독 가능한 매체
TWI461567B (zh) * 2008-10-04 2014-11-21 Tokyo Electron Ltd 於直立式批次薄膜形成設備中之薄膜形成方法
US20120315394A1 (en) * 2010-03-19 2012-12-13 Tokyo Electron Limited Film forming apparatus, film forming method, method for optimizing rotational speed, and storage medium
US9200364B2 (en) * 2010-03-19 2015-12-01 Tokyo Electron Limited Film forming apparatus, film forming method, method for optimizing rotational speed, and storage medium
US9136148B2 (en) 2010-05-20 2015-09-15 Tokyo Electron Limited Substrate processing apparatus, control device thereof, and control method thereof
KR20140097984A (ko) * 2013-01-30 2014-08-07 가부시키가이샤 히다치 고쿠사이 덴키 기판 처리 장치, 반도체 장치의 제조 방법 및 기록 매체
US20140213069A1 (en) * 2013-01-30 2014-07-31 Hitachi Kokusai Electric Inc. Substrate Processing Apparatus, Method of Manufacturing Semiconductor Device and Non-transitory Computer-readable Recording Medium
US9437421B2 (en) * 2013-01-30 2016-09-06 Hitachi Kokusai Electric Inc. Substrate processing apparatus, method of manufacturing semiconductor device and non-transitory computer-readable recording medium
KR101686029B1 (ko) * 2013-01-30 2016-12-13 가부시키가이샤 히다치 고쿠사이 덴키 기판 처리 장치, 반도체 장치의 제조 방법 및 기록 매체
US20150170909A1 (en) * 2013-12-17 2015-06-18 Hitachi Kokusai Electric Inc. Method of manufacturing semiconductor device and non-transitory computer-readable recording medium
CN104746040A (zh) * 2013-12-27 2015-07-01 株式会社日立国际电气 衬底处理系统、半导体器件的制造方法及存储介质
US20210159083A1 (en) * 2014-09-30 2021-05-27 Kokusai Electric Corporation Substrate processing device, manufacturing method for semiconductor device, and reaction tube
US10811271B2 (en) 2014-09-30 2020-10-20 Kokusai Electric Corporation Substrate processing device, manufacturing method for semiconductor device, and reaction tube
US10950457B2 (en) * 2014-09-30 2021-03-16 Kokusai Electric Corporation Substrate processing device, manufacturing method for semiconductor device, and reaction tube
US12062546B2 (en) * 2014-09-30 2024-08-13 Kokusai Electric Corporation Substrate processing device, manufacturing method for semiconductor device, and reaction tube
US9698021B2 (en) * 2014-12-30 2017-07-04 Samsung Electronics Co., Ltd. Deposition methods of forming a layer while rotating the substrate in angular increments and methods of manufacturing a semiconductor device using the same
US20160189951A1 (en) * 2014-12-30 2016-06-30 Samsung Electronics Co., Ltd. Methods of forming a layer and methods of manufacturing a semiconductor device using the same
US11542601B2 (en) * 2016-02-09 2023-01-03 Hitachi Kokusai Electric Inc. Substrate processing apparatus and method of manufacturing semiconductor device
US11952664B2 (en) 2016-02-09 2024-04-09 Kokusai Electric Corporation Substrate processing apparatus and method of manufacturing semiconductor device
US11453942B2 (en) * 2017-02-23 2022-09-27 Kokusai Electric Corporation Substrate processing apparatus and method of manufacturing semiconductor device
US11859280B2 (en) 2017-02-23 2024-01-02 Kokusai Electric Corporation Substrate processing apparatus and method of manufacturing semiconductor device
US12203167B2 (en) 2017-02-23 2025-01-21 Kokusai Electric Corporation Substrate processing apparatus and method of manufacturing semiconductor device

Also Published As

Publication number Publication date
JP2004134466A (ja) 2004-04-30
JP4204840B2 (ja) 2009-01-07
WO2004034454A1 (ja) 2004-04-22
TW200423253A (en) 2004-11-01
TWI232518B (en) 2005-05-11
US7713582B2 (en) 2010-05-11
US20080160214A1 (en) 2008-07-03

Similar Documents

Publication Publication Date Title
US7713582B2 (en) Substrate processing method for film formation
US7622396B2 (en) Method of producing a semiconductor device
US7482283B2 (en) Thin film forming method and thin film forming device
JP3947126B2 (ja) 半導体製造装置
US9487861B2 (en) Substrate processing apparatus capable of forming films including at least two different elements
US20080166882A1 (en) Substrate Processing Apparatus and Producing Method of Semiconductor Device
JP4814914B2 (ja) 基板処理装置及び半導体装置の製造方法
JP4356943B2 (ja) 基板処理装置及び半導体装置の製造方法
JP5362782B2 (ja) 基板処埋装置、基板処理方法及び半導体装置の製造方法
JP4695343B2 (ja) 縦型半導体製造装置
JP2005064306A (ja) 基板処理装置
JP2006216597A (ja) 基板処理装置

Legal Events

Date Code Title Description
AS Assignment

Owner name: HITACHI KOKUSAI ELECTRIC INC., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SAKAI, MASANORI;KAGAYA, TORU;SHIMA, NOBUHITO;REEL/FRAME:017128/0284;SIGNING DATES FROM 20051123 TO 20051201

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION