ELECTROSTATIC CHUCK AND METHOD OF MANUFACTURING THE SAME
20230377934 · 2023-11-23
Assignee
Inventors
Cpc classification
C04B37/028
CHEMISTRY; METALLURGY
C04B2235/656
CHEMISTRY; METALLURGY
C04B2235/3891
CHEMISTRY; METALLURGY
International classification
C04B37/00
CHEMISTRY; METALLURGY
Abstract
The present disclosure relates to an electrostatic chuck and a method of manufacturing the same. A problem in that the yield of a wafer is reduced due to a partial destruction phenomenon attributable to thermal expansion of an electrostatic chuck is solved and the lifespan of a wafer is increased by making a coefficient of thermal expansion of a lower plate of an electrostatic chuck similar to a coefficient of thermal expansion of an upper plate of the electrostatic chuck.
Claims
1. An electrostatic chuck comprising an upper plate made of ceramic and having a wafer seated therein, a lower plate bonded to the upper plate, and an adhesive for bonding the upper plate and the lower plate together, wherein the lower plate is sintered and molded at a high temperature under vacuum and pressurization by mixing first powder comprising at least one of aluminum, stainless steel, titanium, and magnesium and second powder comprising at least one of silicon-carbide (SiC), silicon nitride (Si.sub.3N.sub.4), silicon, diamond, carbon nanotubes, and graphene, and a mixing ratio of the first powder and the second powder is 4:6 to 6:4.
2. The electrostatic chuck of claim 1, wherein a ratio of a particle size of the first powder and the second powder is 1:0.05 to 1:0.4.
3. The electrostatic chuck of claim 1, wherein the lower plate is sintered and molded at a temperature of 300° C. to 700° C.
4. The electrostatic chuck of claim 1, wherein the lower plate is sintered and molded at pressure of 10 MPa to 300 MPa.
5. The electrostatic chuck of claim 1, wherein the lower plate is sintered and molded for 30 minutes to 2 hours.
6. A method of manufacturing an electrostatic chuck comprising an upper plate made of ceramic and having a wafer seated therein, a lower plate bonded to the upper plate, and an adhesive for bonding the upper plate and the lower plate together, wherein the lower plate is manufactured by: a first step of preparing first powder comprising at least one of aluminum, stainless steel, titanium, and magnesium; a second step of preparing second powder comprising at least one of silicon-carbide (SiC), silicon nitride (Si.sub.3N.sub.4), silicon, diamond, carbon nanotubes, and graphene; a third step of mixing the first powder and the second powder; and a fourth step of producing a molding body of the lower plate by sintering and molding the mixed powder at a high temperature under vacuum and pressurization, and a ratio of the first powder and the second powder that are mixed in the third step is 4:6 to 6:4.
7. The method of claim 6, wherein a ratio of a particle size of the first powder and the second powder that are mixed in the third step is 1:0.05 to 1:0.4.
8. The method of claim 6, wherein the fourth step is performed at a temperature of 300° C. to 700° C.
9. The method of claim 6, wherein the fourth step is performed at pressure of 10 MPa to 300 MPa.
10. The method of claim 6, wherein the fourth step is performed for 30 minutes to 2 hours.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0018]
[0019]
[0020]
[0021]
[0022]
[0023]
DETAILED DESCRIPTION
[0024] Hereinafter, embodiments of the present disclosure are described in detail with reference to the accompanying drawings so that a person having ordinary knowledge in the art to which the present disclosure pertains may easily practice the embodiments. In reference numerals presented in the drawings, the same reference number indicates the same member.
[0025] In describing the present disclosure, when it is determined that a detailed description of a related known technology may obscure the subject matter of the present disclosure, the detailed description is omitted.
[0026] Terms, such as a first and a second, may be used to describe various components, but the components are not restricted by the terms. The terms are used to only distinguish one component from another component.
[0027]
[0028] Referring to
[0029] The upper plate 210 is made of ceramic having a thin thickness of approximately 1 mm to 5 mm in order to facilitate the transfer of heat to the wafer 20. A material, such as epoxy, is used as the adhesive 230. A material containing a metal component is used a lot as the lower plate 220 for the transfer of heat to the ESC 200.
[0030] The ESC 200 according to an embodiment of the present disclosure can solve a problem in that the adhesive is torn or the upper plate is broken by making a coefficient of thermal expansion of the lower plate 220 identical with a coefficient of thermal expansion of the upper plate 210 or minimizing a difference between the coefficients of thermal expansion of the lower plate 220 and the upper plate 210.
[0031] In the ESC 200 according to an embodiment of the present disclosure, the lower plate 220 is sintered and molded at a high temperature under vacuum and pressurization by mixing first powder including at least one of aluminum, stainless steel, titanium, and magnesium and second powder including at least one of silicon-carbide (SiC), silicon nitride (Si.sub.3N.sub.4), silicon, diamond, carbon nanotubes, and graphene. In this case, it is preferred that the mixing ratio of the first powder and the second powder is 4:6 to 6:4.
[0032] In order to make a coefficient of thermal expansion of the lower plate 220 identical with a coefficient of thermal expansion of the upper plate 210 or minimize a difference between the coefficients of thermal expansion of the lower plate 220 and the upper plate 210, it is very important to adjust the ratio of the particle size of the first powder and the second powder in addition to the mixing ratio of the first powder and the second powder.
[0033] In the ESC 200 according to an embodiment of the present disclosure, it is preferred that the ratio of the particle size of the first powder and the second powder of the lower plate 220 is adjusted in the range of 1:0.05 to 1:0.4.
[0034] It is preferred that the lower plate 220 is sintered and molded at a temperature of 300° C. to 700° C. and pressure of 10 MPa to 300 MPa for 30 minutes to 2 hours.
[0035]
[0036] In
[0037] Referring to
[0038] The results of
TABLE-US-00001 TABLE 1 Ratio of particle size of SiC to AI 1:0.05 1:0.1 1:0.2 1:0.4 Volume ratio (%) of SiC 40 15.21 13.28 13.72 13.81 50 11.45 13.01 13.17 13.03 60 11.05 11.05 11.79 10.79
[0039] The lower plate having a coefficient of thermal expansion within a preferred range can be obtained if the ratio of the particle size of silicon-carbide (SiC), that is, the second powder, to the aluminum alloy (Al6061), that is, the first powder, is adjusted in the range of 1:0.05 to 1:0.4 and the ratio of silicon-carbide (SiC), that is, the second powder, is adjusted in the range of 40 to 60 volume %.
[0040] In this case, if the ratio of the particle size of silicon-carbide (SiC), that is, the second powder, to the aluminum alloy (Al6061), that is, the first powder, is less than 1:0.05, there is a problem in that a heat transfer coefficient is suddenly reduced because the density and dispersibility of the powers is deteriorated and the density is reduced after sintering. Furthermore, if the ratio of the particle size of silicon-carbide (SiC), that is, the second powder, to the aluminum alloy (Al6061), that is, the first powder, is greater than 1:0.4, there is a problem in that the coefficient of thermal expansion is reduced because a bonding force between the particles is reduced.
TABLE-US-00002 TABLE 2 Coefficient of thermal Mixture expansion (10.sup.−6/K) Al-1% SiC (ratio of particle sizes 1:0.2) 22.29 Al-5% SiC (ratio of particle sizes 1:0.2) 23.46 Al-10% SiC (ratio of particle sizes 1:0.2) 22.56 Al-20% SiC (ratio of particle sizes 1:0.2) 21.12 Al-30% SiC (ratio of particle sizes 1:0.2) 19.98 Al-40% SiC (ratio of particle sizes 1:0.2) 13.72 Al-50% SiC (ratio of particle sizes 1:0.2) 13.17 Al-60% SiC (ratio of particle sizes 1:0.2) 11.79 Al-70% SiC (ratio of particle sizes 1:0.2) 10.12 Al-80% SiC (ratio of particle sizes 1:0.2) 10.01
[0041] Table 2 illustrates the results of experiments on a characteristic change according to the ratio of silicon-carbide (SiC) for the mixture of the aluminum alloy (Al6061), that is, the first powder, and silicon-carbide (SiC), that is, the second powder.
[0042] From Table 2, it may be seen that when the ratio of silicon-carbide (SiC) for the mixture of the aluminum alloy (Al6061) and silicon-carbide (SiC) is 40% or less, a desired coefficient of thermal expansion cannot be obtained and when the ratio of silicon-carbide (SiC) for the mixture of the aluminum alloy (Al6061) and silicon-carbide (SiC) is more than 40%, the coefficient of thermal expansion is suddenly improved.
[0043] When the ratio of silicon-carbide (SiC) for the mixture of the aluminum alloy (Al6061) and silicon-carbide (SiC) is more than 60%, a characteristic distribution of the powders is deteriorated because the dispersibility of the powders, that is, a process of the powders being uniformly mixed, is reduced.
[0044]
[0045] Referring to
[0046] In the first powder preparation step S100, first powder 310, that is, molding body powder including at least one of aluminum, stainless steel, titanium, and magnesium, is prepared. When the ease of molding processing is considered, it is preferred that the prepared first powder includes aluminum as a major component of the material of the first powder. For reference, pure aluminum has a coefficient of thermal expansion of 23.8 [μm/° C.], alumina (Al.sub.2O.sub.3) has a coefficient of thermal expansion of 6.7 to 7.7 [μm/° C.], and aluminum-nitride (AlN) has a coefficient of thermal expansion of 4.5 to 5.0 [μm/° C.]. Hereinafter, the unit of a coefficient of thermal expansion is [μm/° C.].
[0047] In the second powder preparation step S200, second powder 320, that is, additive powder including at least one of silicon-carbide (SiC), silicon nitride (Si.sub.3N.sub.4), silicon, diamond, carbon nanotubes, and graphene, is prepared.
[0048] In the second powder 320, that is, additive powder, silicon-carbide (SiC) has a coefficient of thermal expansion of 4.5 to 6.6, silicon nitride (Si.sub.3N.sub.4) has a coefficient of thermal expansion of 2.6, stainless steel (SUS) has a coefficient of thermal expansion of 10 to 18 depending on standards thereof, diamond has a coefficient of thermal expansion of about 1.1, and carbon nanotubes have a coefficient of thermal expansion of 4 to 6 depending on a direction thereof and the content of fine carbon.
[0049] In the powder mixing step S300, the first powder 310, that is, the molding body powder, and the second powder 320, that is, the additive powder, are mixed. As an embodiment, Al6061, that is, an aluminum alloy, may be used as the first powder 310, and silicon-carbide (SiC) may be used as the second powder 320. In this case, it is preferred that the ratio of the particle size of the first powder and the second powder that are mixed is 1:0.05 to 1:0.4.
[0050] In this case, the volume of the second powder 320, that is, additive powder, may be properly adjusted, if necessary. For example, if silicon-carbide (SiC) is used as the second powder 320, the volume of silicon-carbide (SiC) may be increased or decreased within 40% to 60% of the entire mixed powder 330. If Al6061, that is, an aluminum alloy, is used as the first powder 310, a coefficient of thermal expansion of the mixed powder is gradually reduced from a coefficient of thermal expansion of aluminum depending on a mixed ratio thereof. Since it is expected that the second powder that is used as an additive is mixed with the first powder, it is preferred that a material that is advantageous in being pressurized and molded at a high temperature and that more facilitates the adjustment and prediction of a coefficient of thermal expansion of the material is selected as the second powder.
[0051] In the sintering molding step S400, the lower plate 220 is completed by molding the mixed powder as a sintering material by pressurizing the mixed powder. In this case, conditions for such sintering molding, that is, pressure, a temperature, and the time, are variable depending on a state of a desired finished sintering material. Preferably, it is better to perform the sintering molding at pressure of 10 MPa to 300 MPa and a temperature of 300° C. to 700° C. for 30 minutes to 2 hours. The sintering molding step S400 may be performed by using a cold press or a high pressure injection method.
[0052] In some cases, in order to adjust a temperature of the lower plate, an electrode needs to be buried in the lower plate. In this case, after a mold of the lower plate is divided by half and the two molds are separately manufactured, the electrode needs to be buried between the two molds.
[0053]
[0054] That is, as illustrated in
[0055] In an embodiment of the present disclosure, the sintering molding step may be replaced with another method other than the aforementioned powder metallurgy method of pressurizing and molding the mixed powder. For example, the first powder may be first sintered, and a pouring method of first melting the first powder so that bubbles are properly formed in the first powder may be used. Thereafter, a method of melting the first powder through pressurization and filling the molten results with bubbles may be used. Alternatively, a method of first melting another first powder and then adding the second powder may be used.