The present invention generally relates to the field of semiconductor manufacturing equipment. More specifically, it pertains to an improved surface structure for electrostatic chucks (E-Chuck) used within semiconductor process chambers.
During the manufacturing process of semiconductor wafers, electrostatic chucks are widely employed in various process chambers to secure wafers in place during operations such as heating, adsorption, and rotation. These E-Chucks typically undergo surface treatments to enhance their performance and durability.
A common surface treatment method is thermal spraying. However, as semiconductor manufacturing technologies advance, the surface treatment requirements for electrostatic chucks have become increasingly stringent. Traditional thermal spraying techniques often result in coatings with insufficient density and hardness, which is a significant drawback. Furthermore, the frequent loading and unloading of wafers can lead to the wear of the E-Chuck's protrusions. This wear, in turn, may cause particulate matter to adhere to the backside of the wafers, adversely affecting the yield of subsequent manufacturing processes.
Another prevalent surface treatment method involves the use of sintering techniques. Although sintered electrostatic chucks offer higher hardness, the overall manufacturing costs of such E-chucks are significantly increased.
Therefore, designing an electrostatic chuck with a surface structure that exhibits high hardness, high density, and excellent wear resistance while maintaining cost-effectiveness remains a challenge for those skilled in the art.
The primary objective of the present invention is to provide a surface structure for an electrostatic chuck that exhibits high hardness, high density, and excellent wear resistance while also offering reduced manufacturing costs.
The present invention addresses the limitations and challenges associated with traditional electrostatic chucks used in semiconductor manufacturing by introducing an innovative surface structure. This surface structure comprises a substrate, a first protective coating disposed on the substrate, and a second protective coating disposed on the first protective coating. The second protective coating possesses a higher hardness than the first protective coating, thereby providing enhanced wear resistance.
Further distinguishing the present invention, the second protective coating has a lower porosity than the first protective coating. This characteristic ensures higher density, contributing to the overall durability and performance of the electrostatic chuck. The first protective coating is selected from groups comprising metal oxides, fluorides, and nitrides and has a thickness ranging from 100 μm to 250 μm. This layer serves as a robust foundation, protecting the underlying substrate and enhancing the overall wear and corrosion resistance of the ESC.
The second protective coating is also selected from groups comprising metal oxides, fluorides, and nitrides but is thinner, with a thickness ranging from 0.5 μm to 20 μm. Despite its reduced thickness, this layer provides exceptional hardness, ranging from 1000 HV to 1500 HV, and has a porosity of less than 1%. These properties make it highly effective in reducing particulate contamination from the E-Chuck to the wafer, thereby improving the yield of subsequent semiconductor manufacturing processes.
In addition to structural features, the present invention also aims to provide a method for forming the electrostatic chuck surface structure. The method includes forming the first protective coating on the substrate, followed by forming the second protective coating on the first protective coating, with optimized deposition conditions tailored for each layer to achieve the desired properties.
By offering a combination of high hardness, low porosity, and excellent wear resistance in a cost-effective manner, the present invention significantly advances the state of the art in electrostatic chuck technology for semiconductor manufacturing.
The foregoing, as well as additional objects, features and advantages of the invention will be more readily apparent from the following detailed description, which proceeds with reference to the accompanying drawings.
The objects, spirits, and advantages of the preferred embodiments of the present disclosure will be readily understood by the accompanying drawings and detailed descriptions, wherein:
Referring to
The substrate 12 is typically made from conductive or semiconductor materials capable of generating an electrostatic field, which secures semiconductor wafers in place during various manufacturing processes. In this embodiment, the substrate 12 may be fabricated from aluminum, silicon, or other commonly used metals and ceramic materials in the industry.
The substrate 12 serves as the foundational element of the electrostatic chuck, playing a critical role in the overall performance and functionality of the ESC. Generally, the protective layers are deposited on the substrate 12, which is responsible for generating the electrostatic field that holds the semiconductor wafer in position during the manufacturing process.
In this embodiment, the selection of the substrate 12 material must consider several factors. First, the material must be conductive or semiconductor to generate a sufficient electrostatic field. Common materials include aluminum, silicon, and other metals or ceramics compatible with semiconductor manufacturing environments. Additionally, the material should possess high thermal conductivity to ensure uniform heating of the wafer, thereby maintaining process consistency.
Furthermore, the structural integrity of the substrate 12 is another important consideration. It must be sufficiently robust to withstand mechanical stresses generated during wafer loading and unloading processes, as well as thermal stresses during wafer heating. Moreover, the substrate 12 is typically designed with specific geometries to optimize its mechanical properties, such as tensile strength and fracture toughness.
Additionally, prior to the deposition of protective coatings, the substrate 12 undergoes a series of surface preparation steps. These may include cleaning, etching, and priming to ensure the surface is free from contaminants and conducive to the adhesion of subsequent layers. The surface roughness of the substrate 12 may also be controlled within a specific range to optimize the bond strength between the substrate 12 and the first protective coating 13.
The electrical properties of the substrate 12, such as resistivity and dielectric constant, are also adjusted to optimize the electrostatic holding force. These properties are particularly important when handling ultra-thin or irregularly shaped wafers, as they ensure the wafer remains securely fixed throughout the manufacturing process.
Referring again to
The materials for the first protective coating 13 are selected from groups comprising metal oxides, fluorides, and nitrides, such as TiO2, Al2O3, YF3, Er2O3, Gd2O3, Y2O3, etc. These materials are renowned for their excellent thermal stability, corrosion resistance, and mechanical properties, making them ideal choices for this application.
The hardness of the first protective coating 13 is designed to be within the range of 400 HV to 700 HV, providing a balance between mechanical strength and flexibility.
Due to the relatively thick nature of the first protective coating 13, thermal spraying techniques are employed to increase the deposition rate. Depending on the process design, the porosity of the first protective coating 13 ranges from 1% to 5%.
The deposition process is meticulously controlled to achieve the desired properties of the first protective coating 13. For example, an arc current ranging from 200 A to 600 A and a rotating disc speed from 5 RPM to 30 RPM may be used. The choice of carrier gas, such as argon, nitrogen, or helium, and its flow rate are also optimized to ensure high-quality deposition.
Through the careful design and implementation of the first protective coating 13, the present invention significantly enhances the performance and lifespan of the electrostatic chuck. The first protective coating 13 possesses sufficient thickness and strength to increase the wear and corrosion resistance of the substrate.
Referring again to
The second protective coating 14 is formed using Physical Vapor Deposition (PVD) techniques to create a high-density and high-hardness coating. Specifically, the PVD process is highly controlled to achieve the desired properties of the second protective coating 14. Parameters such as chamber temperature, deposition rate, ion source plasma power, and gas flow rate are finely tuned. For example, the chamber temperature may range from 25° C. to 200° C., the deposition rate from 0.1 nm/s to 1.5 nm/s, and other parameters are adjusted accordingly.
Additionally, PVD methods such as electron beam physical vapor deposition (E-Gun PVD) or ion-assisted electron beam physical vapor deposition provide specific advantages in coating quality and process control.
Although the materials for the second protective coating 14 are also selected from groups comprising metal oxides, fluorides, and nitrides, similar to the first protective coating 13, the use of vacuum PVD techniques allows for the production of coatings with higher hardness and lower porosity. The porosity of the second protective coating 14 is designed to be less than 1%, significantly lower than that of the first protective coating 13. This low porosity enhances the hardness and wear resistance of the second protective coating 14, making it ideal for prolonged contact with semiconductor wafers and effectively reducing particle contamination from the E-Chuck to the wafer.
In summary, the second protective coating 14, as the topmost layer in direct contact with the semiconductor wafer, provides exceptionally high hardness, low porosity, and outstanding wear resistance. This enhances the corrosion and wear resistance of the first protective coating 13. Therefore, the surface structure 10 of the electrostatic chuck in this embodiment addresses the shortcomings of existing electrostatic chucks by not only enhancing wear resistance but also significantly reducing the risk of particle contamination, thereby lowering overall manufacturing costs and improving the yield and reliability of the semiconductor manufacturing process.
Referring to
Firstly, referring to step S1, the first protective coating 13 is deposited on the substrate 12 using thermal spraying techniques under specific conditions, such as atmospheric plasma spraying (APS), suspension plasma spraying (SPS), and vacuum plasma spraying (VPS). The three thermal spraying techniques are detailed as follows:
Furthermore, the plasma spraying deposition process is controlled by several parameters to achieve the desired properties of the first protective coating 13. These include an arc current ranging from 200 A to 600 A, a substrate rotation speed from 5 RPM to 30 RPM, and the type of carrier gas, such as argon, nitrogen, or helium. The gas flow rate is adjusted between 30 L/min and 200 L/min, and the process pressure may vary from 1 atmosphere to 1.0×10−2 Torr. The plasma spraying technique is particularly suitable for depositing thick coatings ranging from 100 μm to 250 μm, thereby providing robust protection for the metal components of the electrostatic chuck.
Additionally, an optional but typically beneficial step in the process is the preheating of the substrate 12. The preheating temperature of the substrate 12 can range from 100° C. to 300° C., which aids in improving the adhesion and density of the deposited layer. Moreover, when the thermal properties of the substrate 12 material differ from those of the coating material, preheating the substrate 12 significantly enhances the adhesion between the substrate 12 and the first protective coating 13.
Subsequently, referring to step S2, the second protective coating 14 is deposited on the first protective coating 13 using Physical Vapor Deposition (PVD) techniques under optimized conditions. The PVD techniques include electron beam physical vapor deposition (E-Gun PVD) and ion-assisted electron beam physical vapor deposition. These PVD methods are detailed as follows:
Regardless of whether electron beam physical vapor deposition (E-Gun PVD) or ion-assisted electron beam physical vapor deposition is used, both methods are highly suitable for depositing the second protective coating 14 composed of metal oxides, fluorides, or nitrides, with thicknesses ranging from 0.5 μm to 20 μm.
Furthermore, the optimized conditions mentioned above include chamber temperature, deposition rate, and process pressure. For instance, the chamber temperature ranges from 25° C. to 200° C., the deposition rate from 0.1 nm/s to 1.5 nm/s, and the ion source plasma power can be finely adjusted. Additionally, the electron beam current can range from 0 to 1500 mA, and the voltage from 100 V to 1500 V.
Moreover, the carrier gases used in the PVD techniques, such as argon and oxygen, have flow rates ranging from 5 sccm to 50 sccm and 10 sccm to 200 sccm, respectively, while the process pressure is maintained between 1.0×10−2 and 1.0×10−6 Torr. By optimizing the deposition methods, materials, and process parameters under these conditions, the second protective coating 14 is formed with superior properties that exceed the stringent requirements of semiconductor manufacturing, thereby significantly enhancing performance and extending the lifespan of the electrostatic chuck.
Therefore, compared to traditional methods that utilize sintering to form the surface structure of the electrostatic chuck, the present method employs thermal spraying techniques in conjunction with Physical Vapor Deposition (PVD) methods to generate the first protective coating 13 and the second protective coating 14. This approach effectively reduces the cost of manufacturing the surface structure 10 of the electrostatic chuck.
In summary, the present invention provides a surface structure for an electrostatic chuck and its method of formation, which not only meets the performance and durability requirements of contemporary semiconductor manufacturing processes but also surpasses these requirements. Thus, the present invention represents a significant advancement in the field by cost-effectively delivering a combination of high hardness, low porosity, and excellent wear resistance.
Although the invention has been disclosed and illustrated with reference to particular embodiments, the principles involved are susceptible for use in numerous other embodiments that will be apparent to persons skilled in the art. This invention is, therefore, to be limited only as indicated by the scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 112147939 | Dec 2023 | TW | national |