Method for forming a carbon nanotube pellicle membrane
10712659 ยท 2020-07-14
Assignee
Inventors
- Emily Gallagher (Burlington, VT, US)
- Cedric Huyghebaert (Heverlee, BE)
- Ivan Pollentier (Langdorp, BE)
- Hanns Christoph ADELMANN (Wilsele, BE)
- Marina Timmermans (Bertem, BE)
- Jae Uk Lee (Heverlee, BE)
Cpc classification
G03F1/62
PHYSICS
B82Y30/00
PERFORMING OPERATIONS; TRANSPORTING
B82Y40/00
PERFORMING OPERATIONS; TRANSPORTING
G03F1/64
PHYSICS
International classification
G03F1/22
PHYSICS
G03F1/62
PHYSICS
G03F1/64
PHYSICS
B82Y40/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
The present disclosure relates to a method for forming a carbon nanotube pellicle membrane for an extreme ultraviolet lithography reticle, the method comprising: bonding together overlapping carbon nanotubes of at least one carbon nanotube film by pressing the at least one carbon nanotube film between a first pressing surface and a second pressing surface, thereby forming a free-standing carbon nanotube pellicle membrane. The present disclosure also relates to a method for forming a pellicle for extreme ultraviolet lithography and for forming a reticle system for extreme ultraviolet lithography respectively.
Claims
1. A method for forming a carbon nanotube pellicle membrane for an extreme ultraviolet lithography reticle, the method comprising: bonding together overlapping carbon nanotubes of at least one carbon nanotube film by pressing the at least one carbon nanotube film between a first pressing surface and a second pressing surface, thereby forming a carbon nanotube pellicle membrane, wherein at least one of the first pressing surface or the second pressing surface is provided with a protruding pattern, and wherein the protruding pattern has a pitch smaller than an average length of the overlapping carbon nanotubes of the at least one carbon nanotube film or bundles of carbon nanotubes of the at least one carbon nanotube film.
2. The method according to claim 1, wherein at least two separate carbon nanotube films are pressed between the first pressing surface and the second pressing surface.
3. The method according to claim 1, further comprising, forming a coating on the at least one carbon nanotube film prior to pressing the at least one carbon nanotube film.
4. The method according to claim 3, wherein forming the coating includes forming a coating including at least one material selected from the group consisting of: B, B4C, ZrN, Mo, Ru, SiC, TiN, and a-C.
5. The method according to claim 3, wherein the pressing the at least one carbon nanotube film includes applying a pressure of 0.1 kPa to 30 MPa.
6. The method according to claim 1, wherein the overlapping carbon nanotubes of the at least one carbon nanotube film are in direct contact at locations where the overlapping carbon nanotubes overlap.
7. The method according to claim 1, wherein the protruding pattern is formed by a rough surface, a set of protruding pins, a line pattern, a square grid, or a hexagonal grid.
8. The method according to claim 1, wherein the pitch of the protruding pattern is between 200 nm and 200 m.
9. The method according to claim 1, further comprising heating the at least one carbon nanotube film while pressing the at least one carbon nanotube film.
10. The method according to claim 1, the method further comprising: forming a graphene flake coating layer by depositing graphene flakes on a main surface of the carbon nanotube pellicle membrane.
11. The method according to claim 10, wherein a lateral dimension of the graphene flakes along a main surface of the graphene flakes is between 75 nm and 50 m.
12. The method according to claim 10, wherein the forming of the graphene flake coating layer further comprises heating the carbon nanotube pellicle membrane.
13. The method according to claim 10, wherein the forming of the graphene flake coating layer further comprises applying a pressure to the carbon nanotube pellicle membrane and the graphene flakes.
14. A method for forming a pellicle for extreme ultraviolet lithography, the method comprising: forming the carbon nanotube pellicle membrane according to the method of claim 1, and fixing the carbon nanotube pellicle membrane to a pellicle frame.
15. The method according to claim 14, wherein a coating is formed on the carbon nanotube pellicle membrane and wherein the step of fixing comprises: arranging the carbon nanotube pellicle membrane on a support surface of the pellicle frame, and bonding together the coating of the carbon nanotube pellicle membrane and the support surface of the pellicle frame by pressing the carbon nanotube pellicle membrane and the support surface of the pellicle frame against each other thereby fixing the carbon nanotube pellicle membrane to the support surface of the pellicle frame.
16. The method according to claim 15, wherein the support surface of the pellicle frame is formed by a first material and the coating is formed by a second material, the first material being a metal or a semiconductor, the second material being a metal or a semiconductor.
17. The method according to claim 15, further comprising heating the carbon nanotube pellicle membrane and the pellicle frame while pressing the carbon nanotube pellicle membrane and the support surface of the pellicle frame against each other.
18. The method according to claim 15, wherein the bonding comprises pressing the carbon nanotube pellicle membrane and the support surface of the pellicle frame together using a mechanical pressure while applying a vacuum to the carbon nanotube pellicle membrane and the pellicle frame.
19. A method for forming a reticle system for extreme ultraviolet lithography, the method comprising: forming the pellicle according to the method of claim 14, and mounting the pellicle on a reticle.
20. A carbon nanotube pellicle membrane for an extreme ultraviolet lithography reticle, formed according to the method of claim 1.
Description
BRIEF DESCRIPTION OF THE FIGURES
(1) The above, as well as additional objects and features of the present disclosure, will be better understood through the following illustrative and non-limiting detailed description, with reference to the appended drawings. In the drawings like reference numerals will be used for like elements unless stated otherwise.
(2)
(3)
(4)
(5)
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(7) As illustrated in the figures, the sizes of features, layers and regions are exaggerated for illustrative purposes and, thus, are provided to illustrate the general structures of embodiments of the present disclosure. Like reference numerals refer to like elements throughout.
(8) All the figures are schematic, not necessarily to scale, and generally only show parts which are necessary to elucidate example embodiments, wherein other parts may be omitted or merely suggested.
DETAILED DESCRIPTION
(9) Example embodiments will now be described more fully hereinafter with reference to the accompanying drawings. That which is encompassed by the claims may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided by way of example. Furthermore, like numbers refer to the same or similar elements or components throughout.
(10) The present disclosure will now be described more fully hereinafter with reference to the accompanying drawings, in which currently example embodiments of the disclosure are shown. This disclosure may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided for thoroughness and completeness, and fully convey the scope of the disclosure to the skilled person.
(11) A method for formation of a CNT pellicle membrane 102 for an extreme ultraviolet lithography reticle will now be described with reference to
(12) As is schematically depicted in
(13) The individual CNTs of the depicted CNT film 104 are arranged randomly within the CNT film 104 in the sense that the CNTs 110 are not arranged within the CNT film 104 along a major or predominant direction. However, the CNTs of the CNT film 104 may be provided in ordered manner. The CNTs 110 may for example be provided along a major direction or a plurality of major directions.
(14) The CNTs may also be bundled within the CNT film 104 in the sense that a plurality of individual CNTs form a bundle (i.e., a string or rope-like structure), wherein the CNT film is formed of a plurality of bundles forming a web of aligned or randomly oriented CNT bundles. Accordingly, each element 110 shown in
(15) The individual CNTs 110 (or bundles 110) of the CNT film 104 may be coated with a coating, not shown. The coating may be a metal coating of Mo. The coating may at least partially cover the CNTs 110 in the sense that the individual CNTs or the bundles are partially or completely enclosed by the coating, while still forming network of partially free CNTs within the CNT film 104, as depicted in
(16) Other examples of suitable coatings include B, B.sub.4C, ZrN, Ru, SiC, TiN, a-C, and graphene coatings to give a few examples. In other words, coatings of the above material may equally well be used in the above example. For EUV applications, suitable coatings could include coatings which exhibit a limited absorption of extreme ultraviolet light.
(17) As an alternative, a coating may, instead of being formed around the individual CNTs or bundles 110, be formed as a coating layer on one or both main surfaces of the CNT film 104.
(18) In order to bond together overlapping CNTs 110 of the CNT film 104, the CNT film 104 may be pressed between the first and the second pressing surfaces 106, 108. The pressing surfaces 106, 108 may thus be pressed together so as to apply a mechanical pressure to the CNT film 104.
(19) The applied pressure for coated CNTs 110, may be approximately 0.1 kPa or greater. In an example embodiment, the applied pressure may not exceed 30 MPa. Such a pressure is sufficient for bonding to take place between the coatings of the CNTs 110 at locations where the CNTs 110 overlap, such that the CNTs adhere to each other at the overlapping locations. It is to be noted that bonding need not occur at all overlapping locations. The stated pressures may here refer to an average pressure applied over the area of the CNT film 104.
(20) A so-called cold-weld may be formed between the coatings of the CNTs 110 at locations where the CNTs overlap. The bonding taking place at overlapping locations during the pressing is thus enhancing the strength and integrity of the CNT film 104, thereby forming a free-standing CNT pellicle membrane 102. As may be understood, the pressure may increase locally where the CNTs 110 overlap and stack, which facilitates the bonding together of the overlapping CNTs 110. For reasons of clarity the locations 112 at which the bonding has taken place are indicted by dots or bonds 112 in the lower portion of
(21) More specifically, in the lower portion of
(22) The CNT film 104 may be subjected to a vacuum below 1 mbar during the pressing to facilitate the formation of the bonds 112. In an example embodiment, an ambient pressure in the range of 10.sup.10 mbar to 10.sup.6 bar may be used. To further facilitate the formation of the bonds 112, the CNT film 104 may be heated while being pressed between the pressing surfaces 106, 108. The CNT film 104 may for example be heated to a temperature within the range of 20 to 500 C. while applying the pressure. In an example embodiment, the CNT film 104 may be heated to a temperature below 300 C. while applying the pressure.
(23) A CNT pellicle membrane 102 may alternatively be formed by pressing a CNT film 104 of uncoated CNTs or CNT bundles 110, i.e. CNTs having no coating on its external surfaces. In this case, the CNTs 110 of the CNT film 104 will be in direct contact at locations where the CNTs 110 overlap. Also in this case, the CNT film 104 is pressed between the pressing surfaces 106, 108 as described above. When the CNTs 110 of the CNT film 104 are uncoated, a pressure in the range of 10-30 GPa may be applied in order for the bonding to take place between the overlapping CNTs 110 of the CNT film 104. In this case, the bonding will take place directly between the CNTs 110 of the CNT film 104. Direct bonds, for instance co-valent bonds, may form between carbon atoms of overlapping CNTs of the CNT film 104.
(24) Moreover, a plurality of CNT films 104 may be arranged on top of each other in a stacked manner between the first pressing surface 106 and the second pressing surface 108 in which case bonding will take place within each film and also between the plurality of films, thereby forming the free-standing CNT pellicle membrane 102.
(25) The pressing surfaces 106, 108 of
(26) The material of the anti-sticking coating 114 may be varied to suit different needs and to suit different materials and material combinations. Other examples of anti-sticking coatings which are relevant for the present disclosure includes graphene coatings, coatings comprising a self-assembled monolayer (SAM) comprising thiol and coatings comprising a self-assembled thiol monolayer comprising alkyl end-groups, fluorinated ethylene propylene, and perfluoroalkoxy.
(27) Now referring to
(28) In
(29) Each of the CNT films 204a, 204b are of the type described above in conjunction with
(30) The first pressing surface 206 of
(31) The second pressing surface 208 of
(32) Other patterns than pins and elevated portions may be used on the respective pressing surfaces 206, 208. For instance, line patterns, a square grid, a hexagonal grid, or similar may be used. Moreover, one of the pressing surfaces 206, 208 may be patterned whereas the other may not be. Furthermore, the same type of pattern may be provided on the pressing surfaces 206, 208 or different patterns may be provided. Portions of the pressing surfaces 206, 208 may be patterned whereas other portions may be un-patterned. The protruding pattern 206a, 208a may be a regular pattern or an irregular pattern. The pattern may even be a random pattern, for instance, formed by a rough surface. In example embodiments, the pitch of the patterns/patterns of the respective pressing surfaces 206, 208 are smaller than an average length of the CNTs 210 or of the CNT bundles 210 of the respective CNT films 204a, 204b.
(33) The respective pressing surfaces 206, 208 may be provided with an anti-sticking coating or one of the pressing surfaces 206, 208 may be provided with an anti-sticking coating as described above in conjunction with
(34) In order to bond together overlapping CNTs 210 within the CNT films 204a, 204b and between the CNT films 204a, 204b, the CNT films 204a, 204b are pressed between the first and the second pressing surfaces 206, 208. The pressing surfaces 206, 208 are thus pressed together so as to apply a mechanical pressure to the CNT films 204a, 204b. The applied pressure for the coated CNTs 210 of
(35) In the lower portion of
(36) The CNT films 204a, 204b may be subjected to a vacuum below 1 mbar during the pressing to facilitate the formation of the bonds 212. To further facilitate the formation of the bonds 212, the CNT films 204a, 204b may be heated while being pressed between the pressing surfaces 206, 208. The CNT films 204a, 204b may for example be heated to a temperature within the range of 20 to 500 C. while applying the pressure. In an example embodiment, the CNT films 204a, 204b may be heated to a temperature below 300 C. while applying the pressure.
(37) A free-standing CNT pellicle membrane 202 may alternatively be formed by pressing a plurality of CNT films 204a, 204b of uncoated CNTs 210 with a pressure in the range of 10-30 GPa in order to form the bonds between the overlapping CNTs 210 of the CNT films 204a, 204b, i.e. within the CNT films 204a, 204b as well as between the CNT films 204a, 204b.
(38) An example embodiment of a free-standing CNT pellicle membrane 102, 202 formed in accordance with a method of the above will now be described. According to this embodiment, the membrane 102, 202 includes or is formed of SWCNTs. The individual CNTs 112, 210 may have a diameter of 0.5-2 nm. Alternatively, the membrane 102, 202 includes or is formed of MWCNTs. The individual CNTs 112, 210 may have a diameter of 5-30 nm. For both SWCNTs and MWCNTs the individual CNTs 112, 210 may have an average length >100 m. A typical gap between adjacent CNTs 112, 210 may be 30100 nm. The gap may also be referred to as the pore size.
(39) The CNT pellicle membrane 102, 202 may be formed of two to three CNT films 104, 204a, 204b arranged on top of each other in a stacked manner during the pressing. Similar results may be achieved for four or more CNT films 104, 204a, 204b arranged on top of each other in a stacked manner during the pressing.
(40) In an example embodiment, the thickness of the CNT pellicle membrane 102, 202 may be in the range of 5-50 nm. The thickness of the CNT pellicle membrane 102, 202 may be greater depending on the porosity of the CNT pellicle membrane 102, 202. An important parameter of the CNT pellicle membrane 102, 202 is the amount of atoms/cm.sup.2, as the atoms will absorb or attenuate the EUV light impinging on the CNT pellicle membrane 102, 202. In other words, the number of atoms/cm.sup.2 will influence the transmission efficiency of the CNT pellicle membrane 102, 202. To achieve a transmission of 90% an equivalent thickness of 15 nm graphite or 2.266 g/cm.sup.3 may be used in the CNT pellicle membrane 102, 202. These values roughly correspond to 1.7.Math.10.sup.17 carbon atoms/cm.sup.2 of the pellicle membrane 102, 202. With this insight at hand it is understood that what is important is to form or build a strong CNT membrane 102, 202 with or without coatings which CNT membrane 102, 202 has desired particle retention properties while still having no more than 1.7.Math.10.sup.17 carbon atoms/cm.sup.2 or a carbon atom density no greater than 2.266 g/cm.sup.3.
(41) Membranes having the above characteristics have been subjected to extensive measurements aiming at determining the above characteristics as well as how the membranes works for EUV pellicle applications in practice. The diameter and the average length of the CNTs are mainly set in the course of producing the CNT films 104, 204a, 204b used to form the CNT pellicle membrane 102, 202. Also the gap or pore size is impacted by how densely the CNTs are arranged within the CNT films 104, 204a, 204b used. However, the pore size the CNT pellicle membrane 102, 202 being formed will also be impacted on the number of CNT films 104, 204a, 204b used. A larger number of CNT films 104, 204a, 204b will result in a denser CNT pellicle membrane 102, 202, i.e., a CNT pellicle membrane 102, 202 having a smaller pore size. In general, a denser or less porous CNT pellicle membrane 102, 202 may exhibit better particle retention but may suffer from greater absorption of extreme ultraviolet light. In practice also the diameter and the average length of the CNTs will impact the porosity of the CNT pellicle membrane 102, 202. SEM and TEM may be used to measure the above parameters.
(42) Membranes having the above characteristics have exhibited a high stability to extreme ultraviolet light. A typical transmission loss for a CNT membrane following 100 wafer exposures has been measured to be less than 0.1%. The transmission of extreme ultraviolet light is typically >90% which is a desired value for EUV pellicle applications. Examples of processes for synthesis of SWCNTs and MWCNTs include techniques based on arc-discharge methods, laser ablation, and CVD methods including floating catalyst (aerosol) CVD synthesis. Non-limiting examples of aerosol synthesis techniques is found in WO 2005/085130. An example process for forming aligned CNTs is found in US2016/0083872.
(43) Now referring to
(44) As an example, a lateral dimension of the graphene flakes 302 along a main surface thereof may typically be between 75 nm and 50 m. The larger the graphene flakes 302 become, the greater number of pores are typically covered by an individual graphene flake 302.
(45) In an example embodiment, the graphene flakes 302 may be arranged on the CNT pellicle membrane 102 so as to partially overlap. More specifically, the graphene flakes 302 may be arranged to overlap adjacent graphene flakes 302, as depicted in
(46) The graphene flake coating layer 300 may be formed on the CNT pellicle membrane 102 by applying a suspension comprising an alcohol and the graphene flakes 302 to the CNT pellicle membrane 102. The alcohol may thereafter be evaporated, leaving the graphene flakes 302 on the nanotube pellicle membrane 102. By applying the suspension comprising alcohol the nanotube pellicle membrane 102 may undergo densification while depositing the graphene flake coating layer 300.
(47) The suspension may be applied to the nanotube pellicle membrane 102, by soaking the nanotube pellicle membrane 102 with the suspension. Following this the nanotube pellicle membrane 102 may be rinsed in pure alcohol such as ethanol to remove excessive graphene flakes 302. The alcohol is then evaporated, leaving the graphene flakes 302 on the nanotube pellicle membrane 102. The alcohol may be ethanol however other alcohols may also be used. Alternatively, a solution comprising the graphene flakes 302 and an aqueous or organic media (e.g., N,N-dimethylformamide, dimethyl sulfoxide, N-methyl-2-pyrrolidone) may be used. Moreover, the graphene flakes 302 may also be applied to the CNT pellicle membrane 102 using other techniques such as spray coating, air-brushing or spin-coating.
(48) The CNT pellicle membrane 102 may be heated up to a temperature of 1500 C. during the formation of the graphene flake coating layer 300. In an example embodiment, the CNT pellicle membrane 102 may be heated up to a temperature of 600 C. during the formation of the graphene flake coating layer 300.
(49) A mechanical pressure of 0.1 kPa to 30 MPa may be applied to the CNT pellicle membrane 102 and the graphene flakes 302 when forming the graphene flake coating layer 300. The pressure of 0.1 kPa to 30 MPa is relevant in the case when the CNTs 110 of the CNT pellicle membrane 102 are coated, as disclosed above. Similarly, a pressure of 10-30 GPa is relevant when the CNTs 110 of the CNT pellicle membrane 102 are un-coated as disclosed above.
(50) Now referring to
(51) In the following, it will be described how a CNT pellicle membrane 102, 202 having coated CNTs of the above described kind may be fixed to a pellicle frame 402 with reference to
(52) A coating is formed on the CNT pellicle membrane 102, 202. The coating may be formed on the CNT pellicle membrane 102, 202 in a manner as described above. The coating may be formed prior to or subsequent to the pressing of the CNT film 104 or films 204a, 204b, also as described above. Alternatively, a separate or additional coating may be formed on the CNT pellicle membrane 102, 202, for the purpose of facilitating attachment to the pellicle frame 402. In either case, a coating may be formed at an entire main surface of the CNT pellicle membrane 102, 202 or only at a peripheral region of the CNT pellicle membrane 102, 202. By peripheral region is intended a region of the CNT pellicle membrane 102, 202 which is to be arranged in abutment with and to be fixed to the pellicle frame 402.
(53) The coated CNT pellicle membrane 102, 202 that is to be fixed to the pellicle frame 402 is arranged on a support surface 402a of the pellicle frame 402. The support surface 402a of the pellicle frame is typically an upper surface of the pellicle frame 402.
(54) For handling purposes, the CNT pellicle membrane 102, 202 may be arranged on a carrier or a temporary substrate (not shown). The CNT pellicle membrane 102, 202 may be transferred to the pellicle frame 402. The main surface of the CNT pellicle membrane 102, 202 facing away from the carrier may be arranged in abutment with the pellicle support surface 402a.
(55) The coating of the CNT pellicle membrane 102, 202 and the pellicle support surface 402a are then bonded together by pressing the CNT pellicle membrane 102, 202 and the pellicle support surface 402a against each other. The CNT pellicle membrane 102, 202 will thereby be fixed to the support surface 402a of the pellicle frame given that a sufficient pressure is used. A pressure of 0.1 kPa to 30 MPa is generally sufficient for bonding together the CNT pellicle membrane 102, 202 and the support surface 402a of the pellicle frame 402, given that the CNTs or CNT bundles 110, 210 of the CNT pellicle membrane 102, 202 are coated as described above. If a carrier is used for handling the CNT pellicle membrane 102, 202, the carrier may be removed from the CNT pellicle membrane 102, 202 prior to or subsequent to the bonding of the CNT pellicle membrane 102, 202 to the pellicle frame 402.
(56) In order to bond together the coated CNT pellicle membrane 102, 202 and the pellicle support surface 402a, the support surface 402a is typically formed by a first material and the coating of the CNTs is typically formed by a second material. Several different material combinations or systems will work for bonding together the CNT pellicle membrane 102, 202 and the pellicle support surface 402a.
(57) The first material may be a metal or a semiconductor, the second material may be a metal or a semiconductor. Typically, the material of the support surface 402a and the material of the coating are different materials. Examples of relevant material combinations or systems which may bonded together are Ru and Ge, Pd and Ge, Ru and Si, and Nb and Si. The above examples may be bonded together by being cold welded, while forming a eutectic. The skilled person realizes that other material combinations may be used to bond together the coated CNT pellicle membrane 102, 202 and the pellicle support surface 402a and that the required pressure may vary for the different materiel combinations being used. For instance, the support surface 402a of the pellicle frame 402 may formed by a first metal and the coating of the CNT pellicle membrane 102, 202 may be formed by a second metal. It may thereby be possible to form a eutectic of the first metal and the second metal during the pressing by selecting a material combination capable of forming a eutectic.
(58) Further, the material of the support surface 402a and the material of the coating may be the same material.
(59) Furthermore, as described above, a low pressure and/or an elevated temperature may facilitate the fixing or cold welding of the CNT pellicle membrane 102, 202 to the support surface 402a of the pellicle frame 402.
(60) The pellicle frame 402 may be formed of the same material as the support surface 402a or may be of a different material. In other words, the pellicle frame 402 may include a frame body onto which the material forming the support surface 402a is applied. The support surface 402a may for instance be formed as a thin metal or semiconductor coating on top of an upper surface of the pellicle frame 402. By this arrangement, the properties of the support surface 402a and the pellicle frame 402 may be tailored independent of each other. For instance, the pellicle frame 402 or frame body may be permeable to air, which reduces the risk of damaging the CNT pellicle membrane 102, 202 when the pellicle 400 is subjected to pressure fluctuations, which for example may occur when transferred into a vacuum environment. The pellicle frame 402 may for instance be formed by Si, SiN, SiO.sub.2, or quartz. Other materials for the pellicle frame 202 include metal, plastic or ceramic materials to give a few examples.
(61) The method may further comprise stretching the CNT pellicle membrane 102, 202 in a lateral direction prior to arranging the membrane 102, 202 on the pellicle frame 402. By pre-stretching the CNT pellicle membrane 102, 202, sagging of the membrane 102, 202 may be counteracted. In other words, may exhibit a reduced sagging if stretched in a lateral direction prior to being arranged on the pellicle frame 402. In an example embodiment, a tensile stress of approximately 100 MPa or more may be introduced in the CNT pellicle membrane 102, 202. This may translate to a membrane deflection of less than 0.5 mm for a pellicle of typical dimensions.
(62) Pre-stretching the CNT pellicle membrane 102, 202 may include transferring the CNT pellicle membrane 102, 202 to an intermediate stretchable support. The CNT pellicle membrane 102, 202 may adhere to the stretchable support due to attractive forces at the surface interface between the CNT pellicle membrane 102, 202 and the stretchable support. Any suitable type of stretchable support may be used, such as a stretchable or elastic membrane. The stretchable support may be arranged in a stretching tool adapted to stretch the stretchable support wherein the CNT pellicle membrane 102, 202 may be stretched. The CNT pellicle membrane 102, 202 may subsequently be transferred to the pellicle frame 402. The stretchable support may thereafter be removed from the CNT pellicle membrane 102, 202.
(63) Tensile stress may also be introduced in the CNT pellicle membrane 102, 202 by other means such as by subjecting the CNT pellicle membrane to a thermal treatment process. The thermal treatment process may include heating the CNT pellicle membrane to an elevated temperature (i.e., above room temperature). Additionally or alternatively the thermal treatment process may include cooling the CNT pellicle membrane to a reduced temperature (i.e., below room temperature). Also, applying a coating to the CNT pellicle membrane may increase the tensile stress in CNT pellicle membrane.
(64) Still referring to
(65) Referring now to
(66) The method 500 comprises, step 502, bonding together overlapping CNTs 110, 210 of at least one CNT film 104, 204a, 204b by pressing the at least one CNT film 104, 204a, 204b between a first pressing surface 106, 206 and a second pressing surface 108, 208, thereby forming a free-standing CNT pellicle membrane 102, 202.
(67) The method 500 may further comprise, step 504, forming a coating on the at least one CNT film 104, 204a, 204b prior to pressing the at least one CNT film 104, 204a, 204b.
(68) The method 500 may further comprise, step 506, heating the at least one CNT film 104, 204a, 204b while pressing 502.
(69) The method 500 may further comprise, step 508, forming a coating on the CNTs 110, 210 subsequent to pressing 502, wherein forming 508 the coating may include forming a coating including a material selected from the group consisting of: B, B.sub.4C, ZrN, Mo, Ru, TiN, SiC, a-C, and graphene.
(70) The method 500 may further comprise, step 510, forming a graphene flake coating layer 300 by depositing graphene flakes 302 on a main surface of the CNT pellicle membrane 102, 202. It should be noted that if both steps 508 and 510 are to be performed, step 510 may be performed prior to step 508. The coating formed in step 508 may accordingly be formed to cover the graphene flake coating layer.
(71) The method 500 may further comprise, fixing, step 512, a CNT pellicle membrane 102, 202 to a pellicle frame 402 for forming a pellicle 400.
(72) The method 500 may further comprise, mounting, step 514, the pellicle 400 to a reticle 410 for forming a reticle system 412.
(73) In the above the disclosure has mainly been described with reference to a limited number of embodiments. However, as is readily appreciated by a person skilled in the art, other embodiments than the ones disclosed above are equally possible within the scope of the disclosure, as defined by the appended claims.
(74) Additionally, variations to the disclosed embodiments can be understood and effected by the skilled person in practicing the claimed disclosure, from a study of the drawings, the disclosure, and the appended claims. In the claims, the word comprising does not exclude other elements or steps, and the indefinite article a or an does not exclude a plurality. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measured cannot be used to advantage.
(75) While some embodiments have been illustrated and described in detail in the appended drawings and the foregoing description, such illustration and description are to be considered illustrative and not restrictive. Other variations to the disclosed embodiments can be understood and effected in practicing the claims, from a study of the drawings, the disclosure, and the appended claims. The mere fact that certain measures or features are recited in mutually different dependent claims does not indicate that a combination of these measures or features cannot be used. Any reference signs in the claims should not be construed as limiting the scope.