Reactor manifolds

Information

  • Patent Grant
  • 11492701
  • Patent Number
    11,492,701
  • Date Filed
    Monday, March 9, 2020
    4 years ago
  • Date Issued
    Tuesday, November 8, 2022
    2 years ago
Abstract
Herein disclosed are systems and methods related to semiconductor processing device including a manifold including a bore configured to deliver a gas to a reaction chamber, the manifold including a first block mounted to a second block, the first and second mounted blocks cooperating to at least partially define the bore. A supply channel provides fluid communication between a gas source and the bore, and the supply channel is disposed at least partially in the second block. A metallic seal is disposed about the bore at an interface between the first and second block. Advantageously, the metallic seal improves sealing between the interface between the first block and the second block.
Description
BACKGROUND
Field

The field relates generally to manifolds for vapor deposition, and, in particular, to manifolds for improving the quality of deposition in an atomic layer deposition (ALD) reactor.


Description of the Related Art

There are several vapor deposition methods for depositing thin films on surfaces of substrates. These methods include vacuum evaporation deposition, Molecular Beam Epitaxy (MBE), different variants of Chemical Vapor Deposition (CVD) (including low-pressure and organometallic CVD and plasma-enhanced CVD), and Atomic Layer Deposition (ALD).


In an ALD process, one or more substrates with at least one surface to be coated are introduced into a deposition chamber. The substrate is heated to a desired temperature, typically above the condensation temperatures of the selected vapor phase reactants and below their thermal decomposition temperatures. One reactant is capable of reacting with the adsorbed species of a prior reactant to form a desired product on the substrate surface. Two, three or more reactants are provided to the substrate, typically in spatially and temporally separated pulses.


In an example, in a first pulse, a first reactant representing a precursor material is adsorbed largely intact in a self-limiting process on a wafer. The process is self-limiting because the vapor phase precursor cannot react with or adsorb upon the adsorbed portion of the precursor. After any remaining first reactant is removed from the wafer or chamber, the adsorbed precursor material on the substrate reacted with a subsequent reactant pulse to form no more than a single molecular layer of the desired material. The subsequent reactant may, e.g., strip ligands from the adsorbed precursor material to make the surface reactive again, replace ligands and leave additional material for a compound, etc. In an unadulterated ALD process, less than a monolayer is formed per cycle on average due to steric hindrance, whereby the size of the precursor molecules prevent access to adsorption sites on the substrate, which may become available in subsequent cycles. Thicker films are produced through repeated growth cycles until the target thickness is achieved. Growth rate is often provided in terms of angstroms per cycle because in theory the growth depends solely on number of cycles, and has no dependence upon mass supplied or temperature, as long as each pulse is saturative and the temperature is within the ideal ALD temperature window for those reactants (no thermal decomposition and no condensation).


Reactants and temperatures are typically selected to avoid both condensation and thermal decomposition of the reactants during the process, such that chemical reaction is responsible for growth through multiple cycles. However, in certain variations on ALD processing, conditions can be selected to vary growth rates per cycle, possibly beyond one molecular monolayer per cycle, by utilizing hybrid CVD and ALD reaction mechanisms. Other variations maybe allow some amount of spatial and/or temporal overlap between the reactants. In ALD and other sequential vapor deposition variations thereof, two, three, four or more reactants can be supplied in sequence in a single cycle, and the content of each cycle can be varied to tailor composition.


During a typical ALD process, the reactant pulses, all of which are in vapor form, are pulsed sequentially into a reaction space (e.g., reaction chamber) with removal steps between reactant pulses to avoid direct interaction between reactants in the vapor phase. For example, inert gas pulses or “purge” pulses can be provided between the pulses of reactants. The inert gas purges the chamber of one reactant pulse before the next reactant pulse to avoid gas phase mixing. To obtain a self-limiting growth, a sufficient amount of each precursor is provided to saturate the substrate. As the growth rate in each cycle of a true ALD process is self-limiting, the rate of growth is proportional to the repetition rate of the reaction sequences rather than to the flux of reactant.


SUMMARY

In one aspect, a semiconductor processing device is provided which includes: a manifold including: a bore configured to deliver a gas to a reaction chamber; a first block mounted to a second block, the first and second mounted blocks cooperating to at least partially define the bore; and a supply channel that provides fluid communication between a gas source and the bore, the supply channel disposed at least partially in the second block. The semiconductor processing device further includes a metallic seal disposed about the bore at an interface between the first and second block.


In some embodiments, the metallic seal is a C seal. The metallic seal can be steel. In some embodiments, the metallic seal can be a W seal. The semiconductor processing device may further include an outlet at a lower portion of the manifold. The supply channel may be angled upwardly away from the outlet and inwardly towards the bore. The first block may include an impingement surface at an upper portion of the manifold, the impingement surface shaped to redirect gas downwardly through the bore to the outlet. The impingement surface and the outlet may be disposed along a longitudinal axis of the bore.


In some embodiments, the semiconductor processing device further includes a third block mounted to and below the second block, a second metallic seal between the second and third blocks and at least partially disposed about the bore, where the second and third blocks cooperate to at least partially define the bore. The outlet may be at least partially defined by the third block.


In some embodiments, the semiconductor processing device further includes a gas dispersion device downstream of the outlet, the gas dispersion device configured to disperse a flow of the gas into a reaction chamber. The semiconductor processing device may further include the reaction chamber downstream of the gas dispersion device, the reaction chamber configured to receive a substrate. In some embodiments, the semiconductor processing device further includes a valve block mounted to the first block and a second metallic seal disposed between the valve block and the first block, a reactant gas valve mounted to or coupled with the valve block.


In another aspect, a semiconductor processing device is provided which includes: a manifold comprising: a bore configured to deliver a gas to a reaction chamber and an impingement surface at an upper portion of the manifold. The semiconductor processing device further includes an outlet at a lower portion of the manifold and a supply channel that provides fluid communication between a gas source and the bore, the supply channel is angled upwardly away from the outlet and inwardly towards the bore, the supply channel oriented to direct gas upwardly towards the impingement surface, and the impingement surface is shaped to redirect gas downwardly through the bore to the outlet.


In some embodiments, the manifold includes a first block mounted to a second block, the first and second mounted blocks cooperating to at least partially define the bore, the first block includes the impingement surface. The semiconductor processing device may further include a metallic seal disposed at least partially about the bore between the first and second blocks. The impingement surface and the outlet may be disposed along a longitudinal axis of the bore. The semiconductor processing device may further include a showerhead below the outlet, the showerhead configured to laterally disperse a flow of the gas. The semiconductor processing device may further include a reaction chamber below the showerhead, the reaction chamber configured to receive a substrate. In some embodiments, the outlet opens without restriction into a reaction chamber configured to house one or more substrates.





BRIEF DESCRIPTION OF THE DRAWINGS

These and other features, aspects and advantages of the present invention will now be described with reference to the drawings of several embodiments, which embodiments are intended to illustrate and not to limit the invention.



FIG. 1 is an exploded perspective view of an embodiment of a manifold of a semiconductor processing device, with inset images showing magnified portions of the manifold.



FIG. 2A is a cross sectional view of the semiconductor processing device of FIG. 1.



FIG. 2B is a cross sectional view of an embodiment of a semiconductor processing device.



FIG. 3A is a schematic cross sectional view of the semiconductor processing device shown in FIGS. 1 and 2A.



FIG. 3B is a schematic cross sectional view of the semiconductor processing device of FIG. 2B.



FIG. 4 is a schematic view of the semiconductor processing device of FIGS. 2B and 3B illustrating the placement of valves.





DETAILED DESCRIPTION

The embodiments disclosed herein can be utilized with semiconductor processing devices configured for any suitable gas or vapor deposition process, including processes that alternate reactant exposures (e.g., pulses) to the substrate. For example, the illustrated embodiments show various systems for depositing material on a substrate using atomic layer deposition (ALD) techniques. Among vapor deposition techniques, ALD has many advantages, including high conformality at low temperatures and fine control of composition during the process. ALD type processes are based on controlled, self-limiting surface reactions of precursor chemicals. Gas phase reactions are avoided by feeding the precursors alternately and sequentially into the reaction chamber. Vapor phase reactants are separated from each other in the reaction chamber, for example, by removing excess reactants and/or reactant by-products from the reaction chamber between reactant pulses. Removal can be accomplished by a variety of techniques, including purging and/or lowering pressure between pulses. Pulses can be sequential in a continuous flow, or the reactor can be isolated and can backfilled for each pulse. Of course, the equipment disclosed herein can be useful for other vapor deposition processes, particularly those in which alternation of reactants is desired, such that processes employed by the equipment may include some degree of thermal decomposition and/or overlap of precursor spatially or temporally.


Briefly, a substrate is loaded into a reaction chamber and is heated to a suitable deposition temperature, generally at lowered pressure. Deposition temperatures are typically maintained below the precursor thermal decomposition temperature but at a high enough level to avoid condensation of reactants and to provide the activation energy for the desired surface reactions. Of course, the appropriate temperature window for any given ALD reaction will depend upon the surface termination and reactant species involved, and processes that allow for either condensation or thermal decomposition can be conducted with equipment described herein.


A first reactant is conducted into the chamber in the form of vapor phase pulse and contacted with the surface of a substrate. Conditions are preferably selected such that no more than about one monolayer of the precursor is adsorbed on the substrate surface in a self-limiting manner. Excess first reactant and reaction byproducts, if any, are purged from the reaction chamber, often with a pulse of inert gas such as nitrogen or argon.


Purging the reaction chamber means that vapor phase precursors and/or vapor phase byproducts are removed from the reaction chamber such as by evacuating the chamber with a vacuum pump and/or by replacing the gas inside the reactor with an inert gas such as argon or nitrogen. Typical purging times for a single wafer reactor are from about 0.05 to 20 seconds, particularly between about 1 and 10 seconds, and still more particularly between about 1 and 2 seconds. However, other purge times can be utilized if desired, such as when depositing layers over extremely high aspect ratio structures or other structures with complex surface morphology is needed, or when a high volume batch reactor is employed. The appropriate pulsing times can be readily determined by the skilled artisan based on the particular circumstances.


A second gaseous reactant is pulsed into the chamber where it reacts with the first reactant bound to the surface. Excess second reactant and gaseous by-products of the surface reaction are purged out of the reaction chamber, preferably with the aid of an inert gas. The steps of pulsing and purging are repeated until a thin film of the desired thickness has been formed on the substrate, with each cycle leaving no more than a molecular monolayer. Some ALD processes can have more complex sequences with three or more precursor pulses alternated, where each precursor contributes elements to the growing film. Reactants can also be supplied in their own pulses or with precursor pulses to strip or getter adhered ligands and/or free by-product, rather than contribute elements to the film. Additionally, not all cycles need to be identical. For example, a binary film can be doped with a third element by infrequent addition of a third reactant pulse, e.g., every fifth cycle, in order to control stoichiometry of the film, and the frequency can change during the deposition in order to grade film composition. Moreover, while described as starting with an adsorbing reactant, some recipes may start with the other reactant or with a separate surface treatment, for example to ensure maximal reaction sites to initiate the ALD reactions (e.g., for certain recipes, a water pulse can provide hydroxyl groups on the substrate to enhance reactivity for certain ALD precursors).


As mentioned above, each pulse or phase of each cycle is preferably self-limiting for ALD reactions. An excess of reactant precursors is supplied in each phase to saturate the susceptible structure surfaces. Surface saturation ensures reactant occupation of all available reactive sites (subject, for example, to physical size or steric hindrance restraints) and thus ensures excellent step coverage over any topography on the substrate. In some arrangements, the degree of self-limiting behavior can be adjusted by, e.g., allowing some overlap of reactant pulses to trade off deposition speed (by allowing some CVD-type reactions) against conformality. Ideal ALD conditions with reactants well separated in time and space provide near perfect self-limiting behavior and thus maximum conformality, but steric hindrance results in less than one molecular layer per cycle. Limited CVD reactions mixed with the self-limiting ALD reactions can raise the deposition speed. While embodiments described herein are particularly advantageous for sequentially pulsed deposition techniques, like ALD and mixed-mode ALD/CVD, the manifold can also be employed for pulsed or continuous CVD processing. Many kinds of reactors capable of ALD growth of thin films, including CVD reactors equipped with appropriate equipment and means for pulsing the precursors, can be employed. In some embodiments a flow type ALD reactor is used, as compared to a backfilled reactor. In some embodiments, the manifold is upstream of an injector designed to distribute gas into the reaction space, particularly a dispersion mechanism such as a showerhead assembly above a single-wafer reaction space.


Many kinds of reactors capable of ALD growth of thin films, including CVD reactors equipped with appropriate equipment and means for pulsing the precursors, can be employed. In some embodiments a flow type ALD reactor is used, as compared to a backfilled reactor. In some embodiments, the manifold is upstream of an injector designed to distribute gas into the reaction space, particularly a dispersion mechanism such as a showerhead assembly above a single-wafer reaction space.


The ALD processes can optionally be carried out in a reaction chamber or space connected to a cluster tool. In a cluster tool, because each reaction space is dedicated to one type of process, the temperature of the reaction space in each module can be kept constant, which improves the throughput compared to a reactor in which is the substrate is heated to the process temperature before each run. A stand-alone reactor can be equipped with a load-lock. In that case, it is not necessary to cool down the reaction chamber or space between each run. These processes can also be carried out in a reactor designed to process multiple substrates simultaneously, e.g., a mini-batch type showerhead reactor.


Various embodiments disclosed herein relate to a semiconductor device, such as a vapor deposition device (e.g., an ALD device, a CVD device, etc.), that includes a manifold for delivering reactant vapor(s) to a reaction chamber. Regardless of the natural state of the chemicals under standard conditions, the reactant vapors may be referred to as “gases” herein. The embodiments disclosed herein can beneficially provide an effective fluid seal for the bore of the manifold. For example, in various embodiments, metallic seals (e.g., C seals) can be provided between adjacent blocks to inhibit the flow of gas (e.g., air) from the outside environs into the manifold. Moreover, the embodiments disclosed herein can provide an extended mixing length by, e.g., directing reactant gas upwardly through the supply channels at an angle and directing the reactant gases back downwardly through the bore. The disclosed embodiments can accordingly provide improved sealing, extended mixing length, and reduced non-uniformities at the substrate.



FIG. 1 illustrates an exploded view of a valve block 112a configured to be mounted to a manifold body 102 of a manifold 100. FIG. 2A is a schematic side sectional view of a semiconductor processing device 10 that can include the manifold 100 to deliver a gas to a reaction chamber (not shown). The semiconductor processing device 10 and manifold 100 shown in FIG. 2A may be generally similar to the semiconductor processing devices and manifolds shown and described in U.S. Pat. No. 9,574,268 and U.S. Patent Publication No. US 2017-0350011, the disclosures of which are incorporated by reference herein in their entirety and for all purposes. There may be various differences between the manifolds described in the U.S. Pat. No. 9,574,268 and U.S. Patent Publication No. US 2017-0350011 and the manifold 100 of FIG. 2A, but the overall functionality and design may be similar to, e.g., FIGS. 6A-6J and/or FIGS. 8A-8F of U.S. Pat. No. 9,574,268 and U.S. Patent Publication No. US 2017-0350011. Furthermore, the manifold of the present disclosure can be combined with the valves of FIG. 2 of U.S. Pat. No. 9,574,268 and U.S. Patent Publication No. US 2017-0350011; and/or combined with the reactant/inert gas sources, gas dispersion mechanism, controller, reaction chamber and vacuum source of FIG. 3A of U.S. Pat. No. 9,574,268 and U.S. Patent Publication No. US 2017-0350011.


The manifold 100 can include the manifold body 102 connected with valve blocks 112a, 112b, shown on opposite sides of the manifold body 102. Reactant valves and inert gas valves (not shown) are disposed on the blocks 112a, 112b, or on other upstream blocks (not shown). An inert gas inlet 120 can supply inert gas to the manifold 100, for example, from an upper portion of the manifold 100. The manifold body 102 comprises multiple blocks stacked on one another to at least partially define a bore 130 along which gas(es) flow, including, for example, an upper block 104, an intermediate block 106, and a lower block 108. In the arrangement of FIG. 2A, the intermediate block 106 comprises a sub-block 106a and a sub-block 106b. The lower block 108 comprises a first sub-block 108a, a second sub-block 108b, and a third sub-block 108c. As explained in U.S. Pat. No. 9,574,268 and U.S. Patent Publication No. US 2017-0350011, the use of multiple blocks and sub-blocks can enable a modular construction of the manifold 100 which can enable the use of internal channels with curved or angled shapes and other internal lumens.



FIG. 2A is a modified version of the manifold described with respect to FIGS. 6A-6J of U.S. Pat. No. 9,574,268 and U.S. Patent Publication No. US 2017-0350011. The sub-blocks 108a-108c can define an extended mixing length pathway 180 having a first lateral portion 180a, an offset axial portion 180b, and a second lateral portion 180b. The pathway 180 can provide an extended mixing length downstream of where the supply gases are introduced to the bore 130. The manifold 100 can include a plurality of gas distribution channels, including gas distribution channel 136 shown in FIG. 2A. Supply channels 138a-c convey gases from the distribution channel 136 to the bore 130. As shown, the supply channels 138a-c comprise angled supply channels that are angled downwardly to join the bore 130, where the flow is also downward toward an outlet 132. In the arrangement of FIG. 2A, gas flows through the bore 130, including along the extended mixing length pathway 180, and exits the manifold 100 through the outlet 132. The outlet 132 can be disposed over a dispersion mechanism, such as a showerhead, which can disperse the gas over the substrate in a reaction chamber (not shown).


Although the arrangement of FIG. 2A can beneficially provide an extended mixing length, the extended mixing length pathway 180 and other pathways in the manifold 100 includes curvature and turns which may introduce dead volumes, for example, during purging of reactant gases. The formation of dead volumes can reduce the efficiency and effectiveness of the deposition process. The curved and angled flow pathways of the arrangement shown in FIG. 2A may also create a “throw” onto the substrate. For example, the use of the curved pathway 180 can impart angular momentum to the gas, which can introduce non-uniformities on the substrate.


Moreover, as explained in more detail below in connection with FIG. 3A, and as shown in FIG. 1, the manifold 100 of FIG. 2A utilizes polymeric o-rings 210 (shown in FIG. 2A but labeled in FIGS. 1 and 3A), as seals between adjacent blocks, e.g., between adjacent ones of the vertically stacked blocks 104, 106a, 106b, 108 and associated sub-blocks, as well as between the laterally adjacent valve blocks 112a, 112b (also referred to as “tombstones” herein) and the manifold body 102. However, the use of polymeric o-rings may be permeable to gases, such as atmospheric gases entering the manifold 100 from the outside environs. For example, oxygen and/or moisture may penetrate the polymeric o-rings and enter the bore 130, which can contaminate the deposition processes. Further, as shown in FIG. 1, the o-rings 210 can allow oxygen to enter the manifold body 102, which can create a flaky film at the o-ring interface with the manifold body 102.



FIG. 2B is a schematic side sectional view of an improved semiconductor processing device 10 according to one embodiment. Unless otherwise noted, components of FIG. 2B may be generally similar to or the same as like-numbered components of FIG. 2A. For example, the device 10 of FIG. 2B can include a manifold 100 that defines a bore 130 through a manifold body 102. As with FIG. 2A, in the embodiment of FIG. 2B the manifold 100 can be constructed by mounting multiple blocks to one another. For example, as shown in FIG. 2B, an upper block 104 can be mounted to an intermediate block 106. The intermediate block 106 can be mounted to a lower block 108, which can include an outlet 132. As explained herein and in Paragraph [0049] of U.S. Patent Publication No. 2017/0350011 the use of multiple blocks can enable a modular construction of the module, including curved, angled, or other complex geometries. First and second valve blocks 112a, 112b can also be mounted to the manifold body 102.


Supply lines 138a-138c can be provided to supply gas from corresponding gas distribution channels to the bore 130. Unlike the embodiment of FIG. 2A, the channels 138A-138c of FIG. 2B can be angled upwardly away from the outlet 132 and the downstream reaction chamber relative to their initial entry location in the intermediate block 106. The supply channels 138a-138c can delimit an acute angle as measured between the supply channels 138a-138c and the bore 130. The upper ends of the supply channels 138a-138c can terminate or merge into an impingement surface 214, which may direct the supplied gas(es) downwardly through the bore 130. The impingement surface 214 of FIG. 2B can comprise a curved surface shaped so as to efficiently direct the gases impinging on the surface 214 at an angle back down through the bore 130. In FIG. 2B, the impingement surface 214 and the outlet 132 can be disposed along a linear longitudinal axis of the bore 130. Thus, unlike FIG. 2A in which an inert gas inlet 120 is provided in the upper block 104, in the embodiment of FIG. 2B, the uppermost portion of the upper block 104 is capped, such that the supplied gases, including reactant and inert gases, are provided from the side of the manifold 100.


The bore 130 of the manifold body 102 can deliver reactant and/or inactive gases to a reaction chamber 30 of a reactor 21 by way of the outlet 132 at the bottom of the manifold body 102. A dispersion device 35, such as a showerhead as shown, or a horizontal injection device in other embodiments, can include a plenum 32 in fluid communication with a plurality of openings 19. The reactant vapor can pass through the openings 19 and be supplied into the reaction chamber 30. A substrate support 22 can be configured, or sized and shaped, to support a substrate 36, such as a wafer, within the reaction chamber 30. The dispersed reactant vapor can contact the substrate and react to form a layer (e.g., a monolayer) on the substrate. The dispersion device 35 can disperse the reactant vapor in a manner so as to form a uniform layer on the substrate.


An exhaust line 23 can be in fluid communication with the reaction chamber 30. A vacuum pump 24 can apply suction to the exhaust line 23 to evacuate vapors and excess materials from the reaction chamber 30. The reactor 21 can comprise any suitable type of semiconductor reactor, such as an atomic layer deposition (ALD) device, a chemical vapor deposition (CVD) device, etc. Moreover, the device 10 can comprise a control system 34 in electronic and data communication with the reactor 21. The control system 34 can comprise one or a plurality of processors configured to control the operation of the device 10. Additional components may be provided to manage the operation of the device 10.


Beneficially, the use of the upwardly angled supply channels 138a-138c and the impingement surface 214 can provide an extended mixing length along which gases can become uniformly mixed. Moreover, the extended mixing length provided by the channels 138a-138c can reduce the effects of “throw” or spiral/helical flow effect that may result when the curved pathway 180 of FIG. 2A is used, as well as the dead volumes that may result due to the curved and turning channels along the pathway 180. The “throw” effects may also be mitigated by angling only in a vertical plane, for example, instead of angling laterally.


Also, in FIG. 2B, the o-rings 210 of FIGS. 1 and 2A (and called out in FIG. 3A) can be replaced with metallic seals 212 disposed between adjacent blocks. The metallic seals 212 can comprise any suitable type of metallic seal. The metallic seals 212 can be provided at the interfaces between adjacent blocks and can be disposed at least partially about the bore 130, or at least partially about other adjoining passageways or channels, such as supply channels, gas distribution channels, etc. In the illustrated embodiments, the metallic seals 212 comprise C seals, in which the seal comprises a C-shaped toroidal member, with gap or disconnected portion at an outer periphery of the seal. When adjacent blocks are pressed together, the gap can be reduced such that opposing edges of the seal contact one another. Other types of seals may be suitable, including, for example, W seals. The metallic seal 212 can comprise any suitable type of metal, such as steel. The metallic seal 212 can provide an impermeable barrier to inhibit gases from entering or exiting the bore 130 along the block interfaces.



FIG. 3A is a schematic side view showing the approximate location of some of the many o-rings 210 in the device 10 of FIG. 2A at interfaces between the blocks of the manifold tower or body 102 and valve blocks 112a, 112b. FIG. 3B is a schematic side view showing the approximate locations of metallic rings 212 in the device 10 of FIG. 2B. Unless otherwise noted, the reference numerals of FIGS. 3A-3B represent components that are the same as or generally similar to like-numbered components of FIGS. 2A-2B. FIGS. 3A-3B also illustrate reactant valves 116a, 116b mounted to the respective valve blocks 112a, 112b. A gas injector can be provided downstream of and adjacent the outlet 132 of the bore 130 to provide gases to a downstream reaction chamber (not shown) designed to house one or more substrates. In some embodiments, the gas injector can comprise an open volume between the bore 130 of the manifold 100 and the reaction chamber. In some embodiments, a gas dispersion device 820 can be provided between the bore 130 of the manifold 100 and the reaction chamber. In FIG. 3A, such a gas dispersion device comprises a showerhead plenum and showerhead plate. In other arrangements, the manifold could be provided at the side of a chamber, with or without a gas dispersion device to inject the gases into the reaction chamber.


In the arrangement of FIG. 3A, the device 10 includes fourteen (14) o-rings 210. On the manifold tower 100, each dot shows one half of an o-ring 210 for the o-rings 210 provided on the manifold 100; however, the dots shown between the valve blocks 112a, 112b and the manifold body 102, and between the distribution lines and the valve blocks 112a, 112b, are shown schematically (not in cross-section). There is an o-ring 210 between the Source 1 line and the valve block 112a, between the Source 2 line and the valve block 112b, between a first purge line (Purge N2) and the valve block 112a, and between a second purge line (Purge N2) and the valve block 112b. There is a seal in the form of an o-ring 210 between the first valve block 112a and the first intermediate block 106a, and between the second valve block 112b and the first intermediate block 106a. Two (2) o-rings are provided between the upper block 4 and the first intermediate block 106a. Three (3) o-rings 210 are provided between the first intermediate block 106a and the second intermediate block 106b. There is an o-ring between the second intermediate block 106b and the first lower block 108a, between the first lower block 108a and the second lower block 108b, and between the second lower block 108b and the third lower block 108c.


Turning to FIG. 3B, the construction of the manifold 100 can beneficially reduce the number of seals between blocks, so as to simplify the design and improve sealability. For example, in FIG. 3B, only eight (8) seals 212 are used in the manifold 100. For the illustrated embodiment, metallic seals 212 are employed in place of polymeric o-rings. The metallic seals can be o-rings, W-rings or C-rings. As with FIG. 3A, there is a seal 212 between Source 1 and valve block 112a, between the Source 2 line and the valve block 112b, between the first purge line (Purge N2) and the valve block 112a, and between the second purge line (Purge N2) and the valve block 112b. One (1) metallic seal 212 is provided between the upper block 104 and the intermediate block 106. One (1) metallic seal 212 is disposed between the intermediate block 106 and the lower block 108. One (1) metallic seal 212 is disposed between the valve block 112a and the intermediate block 106, and one (1) metallic seal 212 is disposed between the valve block 112b and the intermediate block 106. Accordingly, in the illustrated embodiment, fewer seals can be used as compared with the implementation of FIG. 3A, particularly within or on the manifold tower or body 102.



FIG. 4 is a schematic system diagram of the device 10 shown in FIGS. 1, 2B and 3B. In the arrangement shown in FIG. 4, four (4) reactant or source gases R1-R4 can be provided sequentially and/or simultaneously, in various combinations, to the manifold 100. For example, the first reactant valve 116a (which can be mounted on valve block 112a) can be configured to controllably supply a first reactant R1 to the manifold 100. The second reactant valve 116b (which can be mounted on valve block 112b) can be configured to controllably supply a second reactant R2 to the manifold 100. The third reactant valve 116c (which may not be mounted on a dedicated valve block) can be configured to controllably supply a third reactant R3 to the manifold 100. The fourth reactant valve 116d (which may not be mounted on a dedicated valve block) can be configured to controllably supply a fourth reactant R4 to the manifold 100. Inert gas valves 114a-114c can be configured to controllably supply a high flow inert gas along the reactant gas supply lines for purging and/or to serve as a carrier gas for the reactants R1-R4. Restrictors 117a-117b can be provided to lower the flow of the inert gas from the valves 114a-114c, for example, when the inert gas is to be used as a carrier gas for the respective reactant R1-R4. FIG. 4 represents only one non-limiting valve scheme that can be provided for use with the manifold of FIGS. 2B and 3B.


Although the foregoing has been described in detail by way of illustrations and examples for purposes of clarity and understanding, it is apparent to those skilled in the art that certain changes and modifications may be practiced. Therefore, the description and examples should not be construed as limiting the scope of the invention to the specific embodiments and examples described herein, but rather to also cover all modification and alternatives coming with the true scope and spirit of the invention. Moreover, not all of the features, aspects and advantages described herein above are necessarily required to practice the present invention.

Claims
  • 1. A semiconductor processing device comprising: a manifold comprising: a bore configured to deliver a gas to a reaction chamber;a first block mounted to a second block, the first and second mounted blocks cooperating to at least partially define the bore; anda supply channel that provides fluid communication between a gas source and the bore, the supply channel disposed at least partially in the second block;a metallic seal disposed about the bore at an interface between the first and second block; andan outlet at a lower portion of the manifold,wherein the supply channel is angled upwardly away from the outlet and inwardly towards the bore.
  • 2. The semiconductor processing device of claim 1, wherein the metallic seal comprises a C seal.
  • 3. The semiconductor processing device of claim 1, wherein the metallic seal comprises steel.
  • 4. The semiconductor processing device of claim 1, wherein the metallic seal comprises a W seal.
  • 5. The semiconductor processing device of claim 1, wherein the first block comprises an impingement surface at an upper portion of the manifold, the impingement surface shaped to redirect gas downwardly through the bore to the outlet.
  • 6. The semiconductor processing device of claim 5, wherein the impingement surface and the outlet are disposed along a longitudinal axis of the bore.
  • 7. The semiconductor processing device of claim 1, further comprising a third block mounted to and below the second block, a second metallic seal between the second and third blocks and at least partially disposed about the bore, wherein the second and third blocks cooperate to at least partially define the bore.
  • 8. The semiconductor processing device of claim 7, wherein the outlet is at least partially defined by the third block.
  • 9. The semiconductor processing device of claim 1, further comprising a gas dispersion device downstream of the outlet, the gas dispersion device configured to disperse a flow of the gas into the reaction chamber.
  • 10. The semiconductor processing device of claim 9, further comprising the reaction chamber downstream of the gas dispersion device, the reaction chamber configured to receive a substrate.
  • 11. The semiconductor processing device of claim 1, further comprising a valve block mounted to the first second block and a second metallic seal disposed between the valve block and the first block, a reactant gas valve mounted to or coupled with the valve block.
  • 12. A semiconductor processing device comprising: a manifold comprising: a bore configured to deliver a gas to a reaction chamber; andan impingement surface at an upper portion of the manifold;an outlet at a lower portion of the manifold; anda supply channel that provides fluid communication between a gas source and the bore,wherein the supply channel is angled upwardly away from the outlet and inwardly towards the bore, the supply channel oriented to direct gas upwardly towards the impingement surface, andwherein the impingement surface is shaped to redirect gas downwardly through the bore to the outlet.
  • 13. The semiconductor processing device of claim 12, wherein the manifold comprises a first block mounted to a second block, the first and second mounted blocks cooperating to at least partially define the bore, the first block comprising the impingement surface.
  • 14. The semiconductor processing device of claim 13, further comprising a metallic seal disposed at least partially about the bore between the first and second blocks.
  • 15. The semiconductor processing device of claim 12, wherein the impingement surface and the outlet are disposed along a longitudinal axis of the bore.
  • 16. The semiconductor processing device of claim 12, further comprising a showerhead below the outlet, the showerhead configured to laterally disperse a flow of the gas.
  • 17. The semiconductor processing device of claim 16, further comprising the reaction chamber below the showerhead, the reaction chamber configured to receive a substrate.
  • 18. The semiconductor processing device of claim 12, wherein the outlet opens without restriction into the reaction chamber configured to house one or more substrates.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority to U.S. Provisional Application No. 62/820,711, filed Mar. 19, 2019, titled REACTOR MANIFOLDS, which is hereby incorporated by reference herein in its entirety.

US Referenced Citations (272)
Number Name Date Kind
1523156 Adams Jan 1925 A
1853045 Gnau Apr 1932 A
3429903 Larson Feb 1969 A
3784631 Menapace et al. Jan 1974 A
3882934 Knoos et al. May 1975 A
3913617 van Laar et al. Oct 1975 A
4222671 Gilmore Sep 1980 A
4401052 Baron et al. Aug 1983 A
4410281 Crookes Oct 1983 A
4422773 Cassaday et al. Dec 1983 A
4649859 Wanlass Mar 1987 A
4747367 Posa May 1988 A
4828224 Crabb et al. May 1989 A
4869284 Scott et al. Sep 1989 A
4889609 Cannella Dec 1989 A
4895107 Yano et al. Jan 1990 A
4907534 Huang et al. Mar 1990 A
4949783 Lakios et al. Aug 1990 A
4951601 Maydan et al. Aug 1990 A
4990047 Wagner et al. Feb 1991 A
5004374 Grey Apr 1991 A
5028724 Ivankovits et al. Jul 1991 A
5071460 Fujiura et al. Dec 1991 A
5080549 Goodwin et al. Jan 1992 A
5106453 Benko et al. Apr 1992 A
5121705 Sugino Jun 1992 A
5131627 Kolenc Jul 1992 A
5166092 Mochizuki et al. Nov 1992 A
5186718 Tepman et al. Feb 1993 A
5192371 Shuto et al. Mar 1993 A
5199483 Bahng Apr 1993 A
5217501 Fuse et al. Jun 1993 A
5223001 Saeki Jun 1993 A
5229615 Brune et al. Jul 1993 A
5248253 Philipossian et al. Sep 1993 A
5252131 Kiyama et al. Oct 1993 A
5284519 Gadgil Feb 1994 A
5286296 Sato et al. Feb 1994 A
5288327 Bhat Feb 1994 A
5350453 Scholosser Sep 1994 A
5388944 Takanabe et al. Feb 1995 A
5391035 Krueger Feb 1995 A
5405446 Nakajima et al. Apr 1995 A
5433785 Saito Jul 1995 A
5462397 Iwabuchi Oct 1995 A
5488925 Kumada Feb 1996 A
5516732 Flegal May 1996 A
5520742 Ohkase May 1996 A
5520743 Takahashi May 1996 A
5525157 Hawkins et al. Jun 1996 A
5538390 Salzman Jul 1996 A
5571330 Kyogoku Nov 1996 A
5586585 Bonora et al. Dec 1996 A
5601651 Watabe Feb 1997 A
5609459 Muka Mar 1997 A
5728223 Murakami et al. Mar 1998 A
5755878 Habuka et al. May 1998 A
5789027 Watkins et al. Aug 1998 A
5846330 Quirk et al. Dec 1998 A
5851294 Young et al. Dec 1998 A
5885358 Maydan et al. Mar 1999 A
5893641 Garcia Apr 1999 A
5938840 Habuka et al. Aug 1999 A
5951771 Raney et al. Sep 1999 A
6036783 Fukunaga et al. Mar 2000 A
6070550 Ravi et al. Jun 2000 A
6079353 Leksell et al. Jun 2000 A
6110529 Gardiner et al. Aug 2000 A
6114227 Leksell et al. Sep 2000 A
6126996 Kirlin et al. Oct 2000 A
6217658 Orczyk et al. Apr 2001 B1
6224676 Nakajima et al. May 2001 B1
6258157 Gordon Jul 2001 B1
6299692 Ku et al. Oct 2001 B1
6302965 Umotoy et al. Oct 2001 B1
6303501 Chen et al. Oct 2001 B1
6331072 Schierholz et al. Dec 2001 B1
6375750 van Os et al. Apr 2002 B1
6416213 Fukunaga Jul 2002 B1
6482740 Soininen et al. Nov 2002 B2
6534133 Kaloyeros et al. Mar 2003 B1
6539891 Lee et al. Apr 2003 B1
6660177 Carr Dec 2003 B2
6783590 Lindfors et al. Aug 2004 B2
6846516 Yang et al. Jan 2005 B2
6878628 Sophie et al. Apr 2005 B2
6881263 Lindfors et al. Apr 2005 B2
6884296 Basceri et al. Apr 2005 B2
6899507 Yamagishi et al. May 2005 B2
6905547 Londergan et al. Jun 2005 B1
6916398 Chen et al. Jul 2005 B2
6921712 Soininen et al. Jul 2005 B2
7018478 Lindfors et al. Mar 2006 B2
7021881 Yamagishi et al. Apr 2006 B2
7045060 Liles et al. May 2006 B1
7163587 Kinnard et al. Jan 2007 B2
7175713 Thakur et al. Feb 2007 B2
7195037 Eidsmore Mar 2007 B2
7204886 Chen et al. Apr 2007 B2
7220669 Hujanen et al. May 2007 B2
7297892 Kelley et al. Nov 2007 B2
7304263 Chang et al. Dec 2007 B2
7311851 Carr Dec 2007 B2
7323581 Gardiner et al. Jan 2008 B1
7402210 Chen et al. Jul 2008 B2
7408225 Shinriki et al. Aug 2008 B2
7416994 Quick Aug 2008 B2
7494927 Kostamo et al. Feb 2009 B2
7591907 Chen et al. Sep 2009 B2
7591957 Carr Sep 2009 B2
7638645 Gordon et al. Dec 2009 B2
7670399 Park Mar 2010 B2
7780785 Chen et al. Aug 2010 B2
7780789 Wu et al. Aug 2010 B2
7846499 Blomberg Dec 2010 B2
7918938 Provencher et al. Apr 2011 B2
7927942 Raaijmakers Apr 2011 B2
8070879 Chen et al. Dec 2011 B2
8137463 Liu et al. Mar 2012 B2
8142847 Shenai-Khatkhate et al. Mar 2012 B2
8152922 Schmidt et al. Apr 2012 B2
8188464 Quick May 2012 B2
8211230 Verghese et al. Jul 2012 B2
8298336 Wang et al. Oct 2012 B2
8372201 Provencher et al. Feb 2013 B2
8399056 Blasco et al. Mar 2013 B2
8425682 Wang et al. Apr 2013 B2
8465801 Schmidt et al. Jun 2013 B2
8668776 Chen et al. Mar 2014 B2
8784563 Schmidt et al. Jul 2014 B2
8809170 Bauer Aug 2014 B2
9029189 Gordon et al. May 2015 B2
9312154 Tran et al. Apr 2016 B2
9359672 Verghese et al. Jun 2016 B2
9388492 White et al. Jul 2016 B2
9394608 Shero et al. Jul 2016 B2
9567672 Kim et al. Feb 2017 B2
9574268 Dunn et al. Feb 2017 B1
9802220 Heys et al. Oct 2017 B2
9863039 Min Jan 2018 B2
9911590 Dussarrat et al. Mar 2018 B2
10131984 Okada Nov 2018 B2
10147597 Lee et al. Dec 2018 B1
10280509 Tzu et al. May 2019 B2
10358407 Hatanpaa et al. Jul 2019 B2
10370761 Dunn et al. Aug 2019 B2
10468291 Verghese et al. Nov 2019 B2
10480072 Shero et al. Nov 2019 B2
10662527 Marquardt May 2020 B2
10683571 Jdira et al. Jun 2020 B2
10844486 Shero et al. Nov 2020 B2
11014866 Hatanpaa et al. May 2021 B2
11047042 McKee et al. Jun 2021 B2
20010003015 Chang et al. Jun 2001 A1
20010006093 Tabuchi et al. Jul 2001 A1
20010054377 Lindfors et al. Dec 2001 A1
20020007790 Park Jan 2002 A1
20020072164 Umotoy et al. Jun 2002 A1
20020081381 DelaRosa et al. Jun 2002 A1
20020113327 Hara Aug 2002 A1
20020170674 Shapiro Nov 2002 A1
20020195055 Grant et al. Dec 2002 A1
20030008072 Lee et al. Jan 2003 A1
20030010451 Tzu et al. Jan 2003 A1
20030019428 Ku et al. Jan 2003 A1
20030056720 Dauelsberg et al. Mar 2003 A1
20030070620 Cooperberg et al. Apr 2003 A1
20030079686 Chen et al. May 2003 A1
20030101938 Ronsse et al. Jun 2003 A1
20030106643 Tabuchi et al. Jun 2003 A1
20030172872 Thakur et al. Sep 2003 A1
20030180460 Strauch et al. Sep 2003 A1
20030194360 Huziwara et al. Oct 2003 A1
20030205096 Gehner et al. Nov 2003 A1
20040016404 Gregg Jan 2004 A1
20040002881 Grant et al. Feb 2004 A1
20040035358 Basceri et al. Feb 2004 A1
20040043557 Haukka et al. Mar 2004 A1
20040113289 Toda et al. Jun 2004 A1
20040118342 Cheng et al. Jun 2004 A1
20040144311 Chen et al. Jul 2004 A1
20040197090 Kudo Oct 2004 A1
20040217217 Han et al. Nov 2004 A1
20040221807 Verghese et al. Nov 2004 A1
20040224504 Gadgil Nov 2004 A1
20050000428 Shero et al. Jan 2005 A1
20050000656 Carr Jan 2005 A1
20050009325 Chung et al. Jan 2005 A1
20050092247 Schmidt et al. May 2005 A1
20050173068 Chen et al. Aug 2005 A1
20050208217 Shinriki et al. Sep 2005 A1
20050241176 Shero et al. Nov 2005 A1
20050252449 Nguyen et al. Nov 2005 A1
20050263197 Eidsmore Dec 2005 A1
20050271812 Myo et al. Dec 2005 A1
20060053833 Martins et al. Mar 2006 A1
20060096540 Choi May 2006 A1
20060266289 Verghese et al. Nov 2006 A1
20070001326 Toda et al. Jan 2007 A1
20070026147 Chen et al. Feb 2007 A1
20070081923 Choe et al. Apr 2007 A1
20070095285 Thakur et al. May 2007 A1
20070098894 Verghese et al. May 2007 A1
20070128864 Ma et al. Jun 2007 A1
20070187634 Sneh Aug 2007 A1
20070194470 Dedontney Aug 2007 A1
20080037968 Kaastra Feb 2008 A1
20080085226 Fondurulia et al. Apr 2008 A1
20080102203 Wu et al. May 2008 A1
20080102208 Wu et al. May 2008 A1
20080115740 You May 2008 A1
20080202416 Provencher et al. Aug 2008 A1
20080241387 Keto Oct 2008 A1
20080254218 Xinjian et al. Oct 2008 A1
20080027161 Vedsted et al. Nov 2008 A1
20090095222 Tam et al. Apr 2009 A1
20090196992 Schmidt et al. Aug 2009 A1
20090215912 Goto et al. Aug 2009 A1
20090320754 Oya et al. Dec 2009 A1
20100003406 Lam et al. Jan 2010 A1
20100024727 Kim et al. Feb 2010 A1
20100048032 Sangam et al. Feb 2010 A1
20100092163 Yeung Apr 2010 A1
20100150756 Chow et al. Jun 2010 A1
20100255198 Cleary Oct 2010 A1
20100266765 White et al. Oct 2010 A1
20100296800 Min et al. Nov 2010 A1
20100310772 Tsuda Dec 2010 A1
20110098841 Tsuda Apr 2011 A1
20110111136 Slevin et al. May 2011 A1
20110116776 Wheeler et al. May 2011 A1
20110128814 Hanada Jun 2011 A1
20110162580 Provencher et al. Jul 2011 A1
20110199855 Hanada Aug 2011 A1
20110223334 Yudovsky et al. Sep 2011 A1
20120079984 Schmidt et al. Apr 2012 A1
20120289057 DeDontney Nov 2012 A1
20120307589 Hanada Dec 2012 A1
20130058835 Salazar-Guillen et al. Mar 2013 A1
20130061759 Laor et al. Mar 2013 A1
20130091933 Tsukada et al. Apr 2013 A1
20130160709 White et al. Jun 2013 A1
20130206338 Tanaka Aug 2013 A1
20130333620 Li et al. Dec 2013 A1
20130333768 Chandrasekharan Dec 2013 A1
20140120031 Yang et al. May 2014 A1
20140141165 Sato et al. May 2014 A1
20140261178 Du Bois et al. Sep 2014 A1
20140284404 Kuah et al. Sep 2014 A1
20150104161 De Mango et al. Apr 2015 A1
20150176126 Ge et al. Jun 2015 A1
20150211112 Cadot et al. Jul 2015 A1
20150232355 Ghaffour et al. Aug 2015 A1
20150240359 Jdira Aug 2015 A1
20150371831 Rozenzon et al. Dec 2015 A1
20150377481 Smith et al. Dec 2015 A1
20160108523 Lee Apr 2016 A1
20160122868 Kim et al. May 2016 A1
20160222508 Schoepp et al. Aug 2016 A1
20160256889 Jones Sep 2016 A1
20160281232 White et al. Sep 2016 A1
20170121818 Dunn et al. May 2017 A1
20170216796 Sameshima Aug 2017 A1
20170350011 Marquardt Dec 2017 A1
20190032206 Hodges Jan 2019 A1
20190195378 Aikawa Jun 2019 A1
20190264326 Doya Aug 2019 A1
20200056286 Shero et al. Feb 2020 A1
20200248308 Marquardt Aug 2020 A1
20200299836 Nandwana Sep 2020 A1
20200354835 Watanabe Nov 2020 A1
20210118668 Nandwana Apr 2021 A1
Foreign Referenced Citations (21)
Number Date Country
101117308 Feb 2008 CN
104561937 Apr 2015 CN
3715644 Dec 1988 DE
H09-186111 Jul 1997 JP
2008-264640 Nov 2008 JP
4667541 Apr 2011 JP
2011-104482 Jun 2011 JP
2011-104483 Jun 2011 JP
2011-246466 Dec 2011 JP
2012-099594 May 2012 JP
2013-075281 Apr 2013 JP
10-1464173 Nov 2014 KR
WO 9010092 Sep 1990 WO
WO 199640690 Dec 1996 WO
WO 0129282 Apr 2001 WO
WO 200218394 Mar 2002 WO
WO 2008002546 Jan 2008 WO
WO 2010047168 Apr 2010 WO
WO 2010114386 Oct 2010 WO
WO 2014163742 Oct 2014 WO
WO 2013111789 May 2015 WO
Non-Patent Literature Citations (11)
Entry
Baxter et al., “Chemical vapour deposition of electrochromic tungsten oxide films employing volatile tungsten(v1) 0×0 alkoxide/ β-diketonate complexes”, Chem. Commun., 1996, pp. 1129-1130.
Bonsu et al., “Synthesis and evaluation of κ2-β-diketonate and β-ketoesterate tungsten(VI) oxo-alkoxide complexes as precursors for chemical vapor deposition of WOx thin films”, Dalton Trans., 2016, 45, pp. 10897-10908.
Browning et al., “Atomic layer deposition of MoS2 films”, Mater. Res. Express 2, 2015, 6 pages.
Buono-Core et al., “Synthesis and evaluation of bis-β-diketonate dioxotungsten(VI) complexes as precursors for the photodeposition of WO3 films”, Polyhedron, 30, 2011, pp. 201-206.
Chisholm et al., “The Molybdenum-Molybdenum Triple Bond. 13.1 Preparations and Characterization of Bis(P- diketonato)tetraalkoxydimolybdenum and -ditungsten Compounds”, Inorg. Chem., 1984, 23, pp. 613-618.
Chisholm et al., “Reactions of Metal-Metal Multiple Bonds. 11.1 A Comparison of the Reactivity of M2(OR)6 (M=M) and M2(OR)4(R‘COCHCOR’)2 (M=M) Compounds (M = Mu, W) with the π-Acid Ligands Co, RC=CR, and RNC”, Inorg. Chem., 1984, 23, pp. 1037-1042.
Doyle, “The Reaction of Some Molybdenum and Tungsten Halides with .beta.-Diketones”, Inorganic Chemistry, vol. 10, No. 10, 1971, pp. 2348-2350.
Kang et al., “High-mobility three-atom-thick semiconducting films with wafer-scale homogeneity”, Nature, Apr. 30, 2015, vol. 520, pp. 656-660.
Lee et al., “Effects of Oxidation State and Crystallinity of Tugsten Oxide Interlayer on Photovoltaic Property in Bulk Hetero-Junction Solar Cell”, J. Phys. Chem. 2012, 116, pp. 13480-13487.
Mazurenko et al., “Synthesis, thermal stability, and IR and UV spectra of molybdenum and tungsten β-diketone complexes”, Probl. Khim. Primen. β [Beta]-Diketonatov Met., (Mater. Vses. Semin.) (1982).
Zelazowlska et al., “WO3-based electrochromic system with hybrid organic-inorganic gel electrolytes”, Journal of Non-Crystalline Solids, 354, 2008, pp. 4500-4505.
Related Publications (1)
Number Date Country
20200299836 A1 Sep 2020 US
Provisional Applications (1)
Number Date Country
62820711 Mar 2019 US