Reduced pattern loading using bis(diethylamino)silane (C8H22N2Si) as silicon precursor

Information

  • Patent Grant
  • 8236708
  • Patent Number
    8,236,708
  • Date Filed
    Friday, August 13, 2010
    14 years ago
  • Date Issued
    Tuesday, August 7, 2012
    12 years ago
Abstract
Aspects of the disclosure pertain to methods of depositing dielectric layers on patterned substrates. In embodiments, dielectric layers are deposited by flowing BIS(DIETHYLAMINO)SILANE (BDEAS), ozone and molecular oxygen into a processing chamber such that a relatively uniform dielectric growth rate is achieved across the patterned substrate surface. The deposition of dielectric layers grown according to embodiments may have a reduced dependence on pattern density while still being suitable for non-sacrificial applications.
Description
FIELD

This application relates to manufacturing technology solutions involving equipment, processes, and materials used in the deposition, patterning, and treatment of thin-films and coatings, with representative examples including (but not limited to) applications involving: semiconductor and dielectric materials and devices, silicon-based wafers and flat panel displays (such as TFTs).


BACKGROUND OF THE INVENTION

Forming dielectric layers on a substrate by chemical reaction of gases is one of the primary steps in the fabrication of modern semiconductor devices. These deposition processes include chemical vapor deposition (CVD) as well as plasma enhanced chemical vapor deposition (PECVD), which uses plasma in combination with traditional CVD techniques.


CVD and PECVD dielectric layers can be used as different layers in semiconductor devices. For example, the dielectric layers may be used as intermetal dielectric layers between conductive lines or interconnects in a device. Alternatively, the dielectric layers may be used as barrier layers, etch stops, or spacers, as well as other layers.


Dielectric layers that are used for applications such as barrier layers and spacers are typically deposited over features, e.g., horizontal interconnects for subsequently formed lines, vertical interconnects (vias), gate stacks, etc., in a patterned substrate. Preferably, the deposition provides a conformal layer. However, it is often difficult to achieve conformal deposition.


For example, it is difficult to deposit a barrier layer over a feature with few or no resulting surface defects or feature deformation. During deposition, the barrier layer material may overloaf, that is, deposit excess material on the shoulders of a via and deposit too little material in the base of the via, forming a shape that looks like the side of a loaf of bread. The phenomena is also known as footing because the base of the via has a profile that looks like a foot. In extreme cases, the shoulders of a via may merge to form a joined, sealed surface across the top of the via. The film thickness non-uniformity across the wafer can negatively impact the drive current improvement from one device to another. Modulating the process parameters alone does not significantly improve the step coverage and pattern loading problems.


Deposition of conformal layers over gate stacks to provide layers that are subsequently etched to form spacers is also challenging. While methods of depositing silicon nitride and silicon oxide layers for spacers using high temperature, low pressure conventional CVD have been developed, the thermal budget for such techniques is becoming too high as semiconductor device geometry continues to shrink. PECVD processes of silicon nitride and silicon oxide deposition can be performed at lower temperatures, but the step coverage and pattern loading results are not as desirable as those obtained with high temperature, low pressure CVD.


Therefore, a need exists for method of depositing conformal films over formed features in a patterned substrate.


BRIEF SUMMARY OF THE INVENTION

Aspects of the disclosure pertain to methods of depositing dielectric layers on patterned substrates. In embodiments, dielectric layers are deposited by flowing BIS(DIETHYLAMINO)SILANE (BDEAS), ozone and molecular oxygen into a processing chamber such that a relatively uniform dielectric growth rate is achieved across the patterned substrate surface. The deposition of dielectric layers grown according to embodiments may have a reduced dependence on pattern density while still being suitable for non-sacrificial applications.


Embodiments of the invention include methods of forming a conformal silicon oxide layer on a patterned substrate in a substrate processing region of a processing chamber. The patterned substrate has a densely patterned region and a sparsely patterned region. The method further includes flowing BDEAS into the substrate processing region, flowing molecular oxygen (O2) into the substrate processing region, and flowing ozone (O3) with a restricted ozone flow rate into the substrate processing region. The method further includes forming the conformal silicon oxide layer on the patterned substrate from the BDEAS, the molecular oxygen and the ozone by chemical vapor deposition. The restricted ozone flow rate is selected such that a thickness of the conformal silicon oxide layer in the densely patterned region is within a conformality percentage of a thickness in the sparsely patterned region.


Additional embodiments and features are set forth in part in the description that follows, and in part will become apparent to those skilled in the art upon examination of the specification or may be learned by the practice of the disclosed embodiments. The features and advantages of the disclosed embodiments may be realized and attained by means of the instrumentalities, combinations, and methods described in the specification.





BRIEF DESCRIPTION OF THE DRAWINGS

A further understanding of the nature and advantages of the disclosed embodiments may be realized by reference to the remaining portions of the specification and the drawings.



FIG. 1 is a flow chart of a conformal silicon oxide deposition process according to disclosed embodiments.



FIG. 2 shows a substrate processing system according to embodiments of the invention.



FIG. 3A shows a simplified representation of a semiconductor processing chamber according to embodiments of the present invention;



FIG. 3B shows a simplified representation of a gas panel and supply lines in relation to a processing chamber.





DETAILED DESCRIPTION OF THE INVENTION

Aspects of the disclosure pertain to methods of depositing dielectric layers on patterned substrates. In embodiments, dielectric layers are deposited by flowing BIS(DIETHYLAMINO)SILANE (BDEAS), ozone and molecular oxygen into a processing chamber such that a relatively uniform dielectric growth rate is achieved across the patterned substrate surface. The deposition of dielectric layers grown according to embodiments may have a reduced dependence on pattern density while still being suitable for non-sacrificial applications.


Embodiments of the invention are directed to methods of forming silicon oxide on a patterned surface of a substrate. Sub-atmospheric CVD (SACVD) and related processes involve flowing a silicon-containing precursor and an oxidizing precursor into a processing chamber to form silicon oxide on the substrate. The silicon-containing precursor may include TEOS and the oxidizing precursor may include ozone (O3), oxygen (O2) and/or oxygen radicals. The inventors have discovered that using BDEAS as the silicon-containing precursor and using relative flowrates disclosed herein reduce the pattern-loading effect (PLE) of the deposited silicon oxide.


Without binding the claim coverage with hypothetical mechanisms which may or may not be entirely correct, it is still beneficial to describe effects which may be occurring during the formation of the silicon oxide. BDEAS is more reactive than TEOS and other alternative silicon-containing precursors but relies more heavily on the presence of the oxidizing precursor due to the absence of oxygen within BDEAS. Coexposure to ozone and oxygen has been found to promote the reaction of BDEAS to form silicon oxide. The flow rates of BDEAS and oxygen (O2) may be increased to increase the growth rate of the silicon oxide. These benefits decrease above a threshold flow rate for each of the precursors. Ozone flow rate exhibits a different characteristic. Low flows of ozone promote silicon oxide growth with a low pattern-loading effect while high flows of ozone exhibit a pronounced pattern-loading effect. Low flows may give rise to a growth process dominated by surface reactions so that high surface area regions of a patterned substrate receive additional deposition relative to low surface area regions. The additional deposition results in a relatively constant film thickness across a patterned substrate having both high and low exposed surface area regions.


In order to better understand and appreciate the invention, reference is now made to FIG. 1 which is a flow chart of a conformal silicon oxide deposition process according to disclosed embodiments and Table I which contains surface roughness measurements taken after deposition. The process begins when a patterned substrate is transferred into a substrate processing region (operation 110). BDEAS, ozone and oxygen (O2) are flowed into the region in operation 120 and a conformal layer of silicon oxide is formed in operation 130. The flow rate of BDEAS may be less than flow rates for TEOS during conventional SACVD (Sub-atmospheric CVD) or HARP (High Aspect Ratio Process) processes because of the comparatively more chemically reactive nature of BDEAS. The flow rate of BDEAS may be less than one of 4 grams per minute (g/min), 3 g/min, 2 g/min, 1 g/min or 500 mg/min, in disclosed embodiments, to reduce the consumption of BDEAS which is not incorporated into the conformal silicon oxide film. The flow rate of BDEAS may be greater than one of 100 mg/min, 200 mg/min, 300 mg/min, 500 mg/min and 800 mg/min, in disclosed embodiments, to maintain productive growth rates of the conformal silicon oxide film. Additional embodiments result from the combination of one of the upper limits with one of the lower limits. The flow of BDEAS may be brought about by bubbling a relatively inert carrier gas like nitrogen (N2) through a liquid supply of BDEAS and delivering a combination of nitrogen and BDEAS to the substrate processing region. The flow rate of nitrogen or a similar gas may be several tens of standard liters per minute (slms).


Characteristics of the formation of silicon oxide depend similarly on the flow rates of oxygen (O2) and BDEAS. Increasing the flow rate of oxygen (O2) from a small value results in an increase in deposition rate. The deposition rate plateaus after a threshold value of the oxygen flow rate is reached. The flow rate of oxygen (O2) may be less than one of 40 standard liters per minute (slm), 30 slm, 25 slm, 20 slm or 15 slm, in disclosed embodiments, to increase the efficient use of oxygen thereby reducing the consumption of oxygen which is not incorporated into the conformal silicon oxide film. The flow rate of oxygen (O2) may be greater than one of 5 slm, 10 slm, 15 slm, 20 slm and 25 slm, in disclosed embodiments, to maintain productive growth rates of the conformal silicon oxide film. Additional embodiments result from the combination of one of the upper limits with one of the lower limits.


The dependence on ozone (O3) has a different character. Though the presence of ozone is necessary for the reaction to proceed, excessive ozone undesirably increases the pattern loading effect (PLE). The flow rate of ozone is accompanied by molecular oxygen, but the flow rates given here include only the ozone contribution to the total flow rate. The flow rate of ozone (O3) may be less than one of 1 slm, 500 sccm, 300 sccm, 200 sccm, 150 sccm, 100 sccm and 70 sccm, in order to avoid a relatively high pattern loading effect. The lower the ozone flow rate, the less the pattern loading effect. The restricted flow of a precursor is sometimes referred to as a choked flow. In this case, the choked flow of ozone may substantially confine the reaction closer to or on the patterned substrate surface, thereby promoting a uniform deposition regardless of the local exposed pattern area density.


The flows of O3, O2 and BDEAS as described above are concurrent, in disclosed embodiments. Flow rates, as used herein, are not necessarily constant during the process. Flow rates of the different precursors may be initiated and terminated in different orders and their magnitudes may be varied. As such, concurrent does not mean that all three flows initiate and terminate together. Concurrent, as used herein, means that a period of time exists during the deposition in which all three flows are non-zero. In disclosed embodiments, all three precursor flows are non-zero for the duration of a deposition process. Unless otherwise indicated, mass flow rate magnitudes indicated herein are given for the approximate peak flow rate used during the process. Flow rate magnitudes indicated herein are for deposition on one side of a pair of 300 mm diameter wafers (area approximately 1400 cm2). Appropriate correction based on deposition area is needed for a different number of wafers, larger or smaller wafers, double sided deposition or deposition on alternative geometry substrates (e.g. rectangular substrates).


The pressure in the substrate processing region is less than for many SACVD and HARP processes (e.g. 600 Torr) due to the reactivity of BDEAS. The pressure during the formation of the conformal silicon oxide film may be less than one of 350 Torr, 300 Torr, 250 Torr, 200 Torr or 150 Torr, in disclosed embodiments, to lessen the risk of uncontrolled reaction. The pressure may be greater than one of 50 Torr, 100 Torr, 150 Ton or 200 Torr, in disclosed embodiments, to maintain productive growth rates. Additional embodiments result from the combination of an upper limits with a lower limit.


The substrate temperature is below a threshold value, in embodiments, also to ensure that the reaction proceeds near or on the surface of the patterned substrate. The temperature of the substrate during the deposition of the conformal silicon oxide is below one of 400° C., 375° C., 350° C., 325° C. and 300° C., in disclosed embodiments. No plasma is present in the substrate processing region in some embodiments. A small ac and/or dc voltage may be applied to the substrate processing region without detriment to the benefits of the deposition process, according to embodiments. Such an excitation should not be considered to deviate from the scope of “essentially” plasma-free or a process having “essentially” no plasma as may be recited in some claims.


Supplying a choked flow of ozone along with TEOS also forms a conformal layer of silicon oxide. However, the film formed thereby possesses greater porosity and a high wet etch rate. Conformal silicon oxide layers formed using BDEAS have greater density and comparatively lower wet etch rate. The wet etch rate of silicon oxide layers formed according to disclosed embodiments possess wet etch rates (using a 1% HF solution) of less than one of 10, 9, 8, 7 or 6 times the wet etch rate of a thermally grown silicon oxide layer, in disclosed embodiments. The greater density and lower wet etch rate of conformal silicon oxide films grown in disclosed embodiments presented herein enables the conformal silicon oxide films (or portions thereof) to be incorporated into finished devices. More porous films, such as those grown with choked ozone and TEOS at low substrate temperature, must generally be removed due to the less resilient structure. As such, material grown using BDEAS and ozone may be left on the patterned substrate during subsequent processing.


The pattern loading was quantified by comparing the horizontal growth of the conformal silicon oxide layer from a vertical feature in a sparsely patterned region and a densely patterned region. An exemplary densely patterned region may have greater number of features than a sparsely patterned region to create the greater exposed surface area within a same area viewed from above the patterned substrate. A densely patterned region may have an exposed vertical area greater than a sparsely patterned region by a multiplicative factor greater than one of 2, 3, 5, 10 or 20, in disclosed embodiments. The thickness of the conformal silicon oxide layer in a densely patterned region may be within one of 30%, 25%, 20%, 15%, 10% and 5% of the thickness of the conformal silicon oxide layer in a sparsely patterned region, in disclosed embodiments. The thickness in each region may be measured on vertical surfaces in which case the growth is in a horizontal direction. Alternatively, the thickness may be measured on a horizontal surface within each region and the growth may then be in the vertical direction. The terms “vertical” and “horizontal” are used throughout to include substantially vertical and substantially horizontal directions which may or may not deviate from the theoretical vertical and horizontal by up to about 10 degrees.


Exemplary Substrate Processing System


Deposition chambers that may implement embodiments of the present invention may include sub-atmospheric chemical vapor deposition (SACVD) chambers and more generally, deposition chambers which allow operation at relatively high pressures without necessarily applying plasma excitation. Specific examples of CVD systems that may implement embodiments of the invention include the CENTURA ULTIMA® SACVD chambers/systems, and PRODUCER® HARP, eHARP and SACVD chambers/systems, available from Applied Materials, Inc. of Santa Clara, Calif.


Embodiments of the deposition systems may be incorporated into larger fabrication systems for producing integrated circuit chips. FIG. 4 shows one such system 200 of deposition, baking and curing chambers according to disclosed embodiments. In the figure, a pair of FOUPs (front opening unified pods) 202 supply substrate substrates (e.g., 300 mm diameter wafers) that are received by robotic arms 204 and placed into a low pressure holding area 206 before being placed into one of the wafer processing chambers 208a-f. A second robotic arm 210 may be used to transport the substrate wafers from the holding area 206 to the processing chambers 208a-f and back.


The processing chambers 208a-f may include one or more system components for depositing, annealing, curing and/or etching a flowable dielectric film on the substrate wafer. In one configuration, two pairs of the processing chamber (e.g., 208c-d and 208e-f) may be used to deposit the flowable dielectric material on the substrate, and the third pair of processing chambers (e.g., 208a-b) may be used to anneal the deposited dielectic. In another configuration, the same two pairs of processing chambers (e.g., 208c-d and 208e-f) may be configured to both deposit and anneal a flowable dielectric film on the substrate, while the third pair of chambers (e.g., 208a-b) may be used for UV or E-beam curing of the deposited film. In still another configuration, all three pairs of chambers (e.g., 208a-f) may be configured to deposit and cure a flowable dielectric film on the substrate. In yet another configuration, two pairs of processing chambers (e.g., 208c-d and 208e-f) may be used for both deposition and UV or E-beam curing of the flowable dielectric, while a third pair of processing chambers (e.g. 208a-b) may be used for annealing the dielectric film. Any one or more of the processes described may be carried out on chamber(s) separated from the fabrication system shown in disclosed embodiments.



FIG. 3A shows a simplified representation of an exemplary semiconductor processing chamber within a semiconductor processing tool 200. This exemplary chamber 310 is suitable for performing a variety of semiconductor processing steps which may include CVD processes, as well as other processes, such as reflow, drive-in, cleaning, etching, and gettering processes. Multiple-step processes can also be performed on a single substrate without removing the substrate from the chamber. Representative major components of the system include a chamber interior 315 that receives process and other gases from a gas delivery system 389, pumping system 388, a remote plasma system (RPS) 355, and a control system 353. These and other components are described below in order to understand the present invention.


The semiconductor processing chamber 310 includes an enclosure assembly 312 housing a chamber interior 315 with a gas reaction area 316. A gas distribution plate 320 is provided above the gas reaction area 316 for dispersing reactive gases and other gases, such as purge gases, through perforated holes in the gas distribution plate 320 to a substrate (not shown) that rests on a vertically movable heater 325 (which may also be referred to as a substrate support pedestal). The heater 325 can be controllably moved between a lower position, where a substrate can be loaded or unloaded, for example, and a processing position closely adjacent to the gas distribution plate 320, indicated by a dashed line 313, or to other positions for other purposes, such as for an etch or cleaning process. A center board (not shown) includes sensors for providing information on the position of the substrate.


Gas distribution plate 320 may be of the variety described in U.S. Pat. No. 6,793,733. These plates improve the uniformity of gas disbursement at the substrate and are particularly advantageous in deposition processes that vary gas concentration ratios. In some examples, the plates work in combination with the vertically movable heater 325 (or movable substrate support pedestal) such that deposition gases are released farther from the substrate when the ratio is heavily skewed in one direction (e.g., when the concentration of a silicon-containing gas is small compared to the concentration of an oxidizer-containing gas) and are released closer to the substrate as the concentration changes (e.g., when the concentration of silicon-containing gas in the mixture is higher). In other examples, the orifices of the gas distribution plate are designed to provide more uniform mixing of the gases.


The heater 325 includes an electrically resistive heating element (not shown) enclosed in a ceramic. The ceramic protects the heating element from potentially corrosive chamber environments and allows the heater to attain temperatures up to about 800° C. In an exemplary embodiment, all surfaces of the heater 325 exposed within the chamber interior 315 are made of a ceramic material, such as aluminum oxide (Al2O3 or alumina) or aluminum nitride.


Reactive and carrier gases are supplied through the supply line 343 into a gas mixing box (also called a gas mixing block) 327, where they are preferably mixed together and delivered to the gas distribution plate 320. The gas mixing block 327 is preferably a dual input mixing block coupled to a process gas supply line 343 and to a cleaning/etch gas conduit 347. A valve 328 operates to admit or seal gas or plasma from the gas conduit 347 to the gas mixing block 327. The gas conduit 347 receives gases from an RPS 355, which has an inlet 357 for receiving input gases. During deposition processing, gas supplied to the plate 320 is vented toward the substrate surface (as indicated by arrows 321), where it may be uniformly distributed radially across the substrate surface, typically in a laminar flow.


Purging gas may be delivered into the chamber interior 315 through the plate 320 and/or an inlet port or tube (not shown) through a wall (preferably the bottom) of enclosure assembly 312. The purging gas flows upward from the inlet port past the heater 325 and to an annular pumping channel 340. An exhaust system then exhausts the gas (as indicated by arrow 322) into the annular pumping channel 340 and through an exhaust line 360 to a pumping system 388, which includes one or more vacuum pumps. Exhaust gases and entrained particles are drawn from the annular pumping channel 340 through the exhaust line 360 at a rate controlled by a throttle valve system 363.


The RPS 355 can produce a plasma for selected applications, such as chamber cleaning or etching native oxide or residue from a process substrate. Plasma species produced in the remote plasma system 355 from precursors supplied via the input line 357 are sent via the conduit 347 for dispersion through the plate 320 to the gas reaction area 316. Precursor gases for a cleaning application may include fluorine, chlorine, and other reactive elements. The RPS 355 also may be adapted to deposit plasma enhanced CVD films by selecting appropriate deposition precursor gases for use in the RPS 355.


The system controller 353 controls activities and operating parameters of the deposition system. The processor 351 executes system control software, such as a computer program stored in a memory 352 coupled to the processor 351. The memory 352 typically consists of a combination of static random access memories (cache), dynamic random access memories (DRAM) and hard disk drives but of course the memory 352 may also consist of other kinds of memory, such as solid-state memory devices. In addition to these memory means the semiconductor processing chamber 310 in a preferred embodiment includes a removable storage media drive, USB ports and a card rack (not shown).


The processor 351 operates according to system control software programmed to operate the device according to the methods disclosed herein. For example, sets of instructions may dictate the timing, mixture of gases, chamber pressure, chamber temperature, plasma power levels, susceptor position, and other parameters of a particular process. The instructions are conveyed to the appropriate hardware preferably through direct cabling carrying analog or digital signals conveying signals originating from an input-output I/O module 350. Other computer programs such as those stored on other memory including, for example, a USB thumb drive, a floppy disk or another computer program product inserted in a disk drive or other appropriate drive, may also be used to operate the processor 351 to configure the semiconductor processing chamber 310 for varied uses.


The processor 351 may have a card rack (not shown) that contains a single-board computer, analog and digital input/output boards, interface boards and stepper motor controller boards. Various parts of the semiconductor processing system 200 conform to the Versa Modular European (VME) standard which defines board, card cage, and connector dimensions and types. The VME standard also defines the bus structure having a 16-bit data bus and 24-bit address bus.


A process for depositing a conformal silicon oxide layer on a patterned substrate or a process for cleaning a chamber can be implemented using a computer program product that is executed by the system controller. The computer program code can be written in any conventional computer readable programming language: for example, 68000 assembly language, C, C++, Pascal, Fortran or others. Suitable program code is entered into a single file, or multiple files, using a conventional text editor, and stored or embodied in a computer usable medium, such as a memory system of the computer. If the entered code text is in a high level language, the code is compiled, and the resultant compiler code is then linked with an object code of precompiled Microsoft Windows® library routines. To execute the linked, compiled object code the system user invokes the object code, causing the computer system to load the code in memory. The CPU then reads and executes the code to perform the tasks identified in the program.


The interface between a user and the controller is via a flat-panel touch-sensitive monitor. In the preferred embodiment two monitors are used, one mounted in the clean room wall for the operators and the other behind the wall for the service technicians. The two monitors may simultaneously display the same information, in which case only one accepts input at a time. To select a particular screen or function, the operator touches a designated area of the touch-sensitive monitor. The touched area changes its highlighted color, or a new menu or screen is displayed, confirming communication between the operator and the touch-sensitive monitor. Other devices, such as a keyboard, mouse, or other pointing or communication device, may be used instead of or in addition to the touch-sensitive monitor to allow the user to communicate with the system controller.


The embodiment disclosed herein relies on direct cabling and a single processor 351. Alternative embodiments comprising multi-core processors, multiple processors under distributed control and wireless communication between the system controller and controlled objects are also possible.



FIG. 3B shows a simplified representation of a gas supply panel 380 in relation to semiconductor processing chamber 310. As discussed above, the portion of semiconductor processing system 200 shown includes semiconductor processing chamber 310 with a heater 325, a gas mixing box 327 with inputs from an inlet tube 343 and a conduit 347, and RPS 355 with input line 357. As mentioned above, the gas mixing box 327 is configured for mixing and injecting deposition gas(es) and cleaning gas(es) or other gas(es) through the inlet tube 343 and the input line 357 to the chamber interior 315.


The RPS 355 is integrally located and mounted below the processing chamber 310 with the conduit 347 coming up alongside the chamber 310 to the gate valve 328 and the gas mixing box 327, located above the chamber 310. Plasma power generator 311 and ozonator 359 are located remote from the clean room. Supply lines 383 and 385 from the gas supply panel 380 provide reactive gases to the gas supply line 343. The gas supply panel 380 includes lines from gas or liquid sources 390 that provide the process gases for the selected application. The gas supply panel 380 has a mixing system 393 that mixes selected gases before flow to the gas mixing box 327. In some embodiments, gas mixing system 393 includes a liquid injection system for vaporizing one or more reactant liquids such as BDEAS, tetraethylorthosilicate (“TEOS”), triethylborate (“TEB”), and triethylphosphate (“TEPO”). Vapor from the liquids is usually combined with a carrier gas, such as helium. Supply lines for the process gases may include (i) shut-off valves 395 that can be used to automatically or manually shut off the flow of process gas into line 385 or line 357, and (ii) liquid flow meters (LFM) 301 or other types of controllers that measure the flow of gas or liquid through the supply lines.


As an example, a mixture including BDEAS as a silicon source may be used with gas mixing system 393 in a deposition process for forming a silicon oxide film. Sources of dopants such as phosphorous and boron may include TEPO and TEB which may also be introduced to gas mixing system 393. Precursors delivered to gas mixing system 393 may be liquid at room temperature and pressure and may be vaporized by conventional boiler-type or bubbler-type hot boxes. Alternatively, a liquid injection system may be used and offers greater control of the volume of reactant liquid introduced into the gas mixing system. The liquid is typically injected as a fine spray or mist into the carrier gas flow before being delivered to a heated gas delivery line 385 to the gas mixing block and chamber. Oxygen (O2) and ozone (O3) flow to the chamber through another gas delivery line 383, to be combined with the reactant gases from heated gas delivery line 385 near or in the chamber. Of course, it is recognized that other sources of dopants, silicon, oxygen and additive precursors may also be used. Though shown as an individual gas distribution line, line 385 may actually comprise multiple lines separated to discourage inter-precursor reactions before the precursors are flowed into chamber interior 315.


As used herein “substrate” may be a support substrate with or without layers formed thereon. The support substrate may be an insulator or a semiconductor of a variety of doping concentrations and profiles and may, for example, be a semiconductor substrate of the type used in the manufacture of integrated circuits. A layer of “silicon oxide” may include minority concentrations of other elemental constituents such as nitrogen, hydrogen, carbon and the like. A gas may be a combination of two or more gases. The terms trench and gap are used throughout with no implication that the etched geometry necessarily has a large horizontal aspect ratio. Viewed from above the surface, gaps may appear circular, oval, polygonal, rectangular, or a variety of other shapes. Gaps may also be a region between two pillars in which case the gaps are not physical separate from other gaps. As used herein, a conformal layer refers to a generally uniform layer of material on a surface in the same shape as the surface, i.e., the surface of the layer and the surface being covered are generally parallel. A person having ordinary skill in the art will recognize that the deposited material likely cannot be 100% conformal and thus the term “generally” allows for acceptable tolerances.


Having disclosed several embodiments, it will be recognized by those of skill in the art that various modifications, alternative constructions, and equivalents may be used without departing from the spirit of the disclosed embodiments. Additionally, a number of well known processes and elements have not been described in order to avoid unnecessarily obscuring the present invention. Accordingly, the above description should not be taken as limiting the scope of the invention.


Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limits of that range is also specifically disclosed. Each smaller range between any stated value or intervening value in a stated range and any other stated or intervening value in that stated range is encompassed. The upper and lower limits of these smaller ranges may independently be included or excluded in the range, and each range where either, neither or both limits are included in the smaller ranges is also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included.


As used herein and in the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a process” includes a plurality of such processes and reference to “the dielectric material” includes reference to one or more dielectric materials and equivalents thereof known to those skilled in the art, and so forth.


Also, the words “comprise,” “comprising,” “include,” “including,” and “includes” when used in this specification and in the following claims are intended to specify the presence of stated features, integers, components, or steps, but they do not preclude the presence or addition of one or more other features, integers, components, steps, acts, or groups.

Claims
  • 1. A method for forming a conformal silicon oxide layer on a patterned substrate in a substrate processing region of a processing chamber, wherein the patterned substrate has a densely patterned region and a sparsely patterned region, the method comprising: flowing BDEAS into the substrate processing region;flowing molecular oxygen (O2) into the substrate processing region;flowing ozone (O3) with a restricted ozone flow rate into the substrate processing region; andforming the conformal silicon oxide layer on the patterned substrate from the BDEAS, the molecular oxygen and the ozone by chemical vapor deposition, wherein the restricted ozone flow rate is selected such that a thickness of the conformal silicon oxide layer in the densely patterned region is within a conformality percentage of a thickness in the sparsely patterned region.
  • 2. The method of claim 1 wherein the operations of flowing BDEAS, molecular oxygen (O2) and ozone (O3) are concurrent.
  • 3. The method of claim 1 wherein the conformality percentage is about 30%.
  • 4. The method of claim 1 wherein the two thicknesses of the conformal silicon oxide layer in the densely and sparsely patterned regions are measured on a substantially-vertical surface of the patterned substrate.
  • 5. The method of claim 1 wherein the two thicknesses of the conformal silicon oxide layer in the densely and sparsely patterned regions are measured on a substantially-horizontal surface of the patterned substrate.
  • 6. The method of claim 1 wherein the operation of flowing BDEAS comprises flowing BDEAS at a rate greater than or about 100 mg/min.
  • 7. The method of claim 1 wherein essentially no plasma is applied to the substrate processing region.
  • 8. The method of claim 1 wherein a pressure in the substrate processing region during formation of the conformal silicon oxide layer is below or about 350 Torr.
  • 9. The method of claim 1 wherein a temperature of the patterned substrate during formation of the conformal silicon oxide layer is below or about 400° C.
  • 10. The method of claim 1 wherein the restricted ozone flow rate is less than about 1 slm.
  • 11. The method of claim 1 wherein the restricted ozone flow rate is less than about 500 sccm.
  • 12. The method of claim 1 wherein the restricted ozone flow rate is less than about 300 sccm.
  • 13. The method of claim 1 wherein an average exposed substantially-vertical area prior to deposition in the densely patterned region exceeds that of the sparsely patterned region by a multiplicative factor of about 2.
  • 14. The method of claim 1 further comprising the operation of flowing a carrier gas which carries the BDEAS into the substrate processing region.
CROSS-REFERENCES TO RELATED APPLICATIONS

This application claims the benefit of U.S. Prov. Pat. App. No. 61/311,949 filed Mar. 9, 2010, and titled “REDUCED PATTERN LOADING USING BIS(DIETHYLAMINO)SILANE (C8H22N2Si) AS SILICON PRECURSOR,” which is incorporated herein by reference for all purposes.

US Referenced Citations (228)
Number Name Date Kind
4147571 Stringfellow et al. Apr 1979 A
4816098 Davis et al. Mar 1989 A
4818326 Liu et al. Apr 1989 A
4931354 Wakino et al. Jun 1990 A
5016332 Reichelderfer et al. May 1991 A
5110407 Ono et al. May 1992 A
5271972 Kwok et al. Dec 1993 A
5393708 Hsia et al. Feb 1995 A
5426076 Moghadam Jun 1995 A
5558717 Zhao et al. Sep 1996 A
5578532 van de Ven et al. Nov 1996 A
5587014 Lyechika et al. Dec 1996 A
5620525 van de Ven et al. Apr 1997 A
5622784 Okaue et al. Apr 1997 A
5635409 Moslehi Jun 1997 A
5665643 Shin Sep 1997 A
5691009 Sandhu Nov 1997 A
5769951 van de Ven et al. Jun 1998 A
5786263 Perera Jul 1998 A
5843233 van de Ven et al. Dec 1998 A
5853607 Zhao et al. Dec 1998 A
5882417 van de Ven et al. Mar 1999 A
5925411 van de Ven et al. Jul 1999 A
5935340 Xia et al. Aug 1999 A
5937308 Gardner et al. Aug 1999 A
5937323 Orczyk et al. Aug 1999 A
6008515 Hsia et al. Dec 1999 A
6009830 Li et al. Jan 2000 A
6024044 Law et al. Feb 2000 A
6087243 Wang Jul 2000 A
6090723 Thakur et al. Jul 2000 A
6114219 Spikes et al. Sep 2000 A
6140242 Oh et al. Oct 2000 A
6146970 Witek et al. Nov 2000 A
6156394 Yamasaki et al. Dec 2000 A
6156581 Vaudo et al. Dec 2000 A
6165834 Agarwal et al. Dec 2000 A
6180490 Vassiliev et al. Jan 2001 B1
6207587 Li et al. Mar 2001 B1
6287962 Lin Sep 2001 B1
6302964 Umotoy et al. Oct 2001 B1
6383954 Wang et al. May 2002 B1
6387207 Janakiraman et al. May 2002 B1
6406677 Carter et al. Jun 2002 B1
6448187 Yau et al. Sep 2002 B2
6503557 Joret Jan 2003 B1
6506253 Sakuma Jan 2003 B2
6508879 Hashimoto Jan 2003 B1
6509283 Thomas Jan 2003 B1
6524931 Perera Feb 2003 B1
6528332 Mahanpour et al. Mar 2003 B2
6544900 Raaijmakers et al. Apr 2003 B2
6548416 Han et al. Apr 2003 B2
6548899 Ross Apr 2003 B2
6559026 Rossman et al. May 2003 B1
6566278 Harvey et al. May 2003 B1
6589868 Rossman Jul 2003 B2
6596654 Bayman et al. Jul 2003 B1
6602806 Xia et al. Aug 2003 B1
6614181 Harvey et al. Sep 2003 B1
6624064 Sahin et al. Sep 2003 B1
6630413 Todd Oct 2003 B2
6645303 Frankel et al. Nov 2003 B2
6660391 Rose et al. Dec 2003 B1
6676751 Solomon et al. Jan 2004 B2
6683364 Oh et al. Jan 2004 B2
6716770 O'Neill et al. Apr 2004 B2
6756085 Waldfried et al. Jun 2004 B2
6762126 Cho et al. Jul 2004 B2
6787191 Hanahata et al. Sep 2004 B2
6794290 Papasouliotis et al. Sep 2004 B1
6818517 Maes Nov 2004 B1
6819886 Runkowske et al. Nov 2004 B2
6830624 Janakiraman et al. Dec 2004 B2
6833052 Li et al. Dec 2004 B2
6833322 Anderson et al. Dec 2004 B2
6835278 Selbrede et al. Dec 2004 B2
6858523 DeBoer et al. Feb 2005 B2
6867086 Chen et al. Mar 2005 B1
6872323 Entley et al. Mar 2005 B1
6890403 Cheung May 2005 B2
6900067 Kobayashi et al. May 2005 B2
6955836 Kumagai et al. Oct 2005 B2
6958112 Karim et al. Oct 2005 B2
7018902 Visokay et al. Mar 2006 B2
7084076 Park et al. Aug 2006 B2
7109114 Chen et al. Sep 2006 B2
7115419 Suzuki Oct 2006 B2
7122222 Xiao et al. Oct 2006 B2
7129185 Aoyama et al. Oct 2006 B2
7148155 Tarafdar et al. Dec 2006 B1
7176144 Wang et al. Feb 2007 B1
7183177 Al-Bayati et al. Feb 2007 B2
7192626 Dussarrat et al. Mar 2007 B2
7205248 Li et al. Apr 2007 B2
7220461 Hasebe et al. May 2007 B2
7297608 Papasouliotis et al. Nov 2007 B1
7335609 Ingle et al. Feb 2008 B2
7399388 Moghadam et al. Jul 2008 B2
7419903 Haukka et al. Sep 2008 B2
7435661 Miller et al. Oct 2008 B2
7456116 Ingle et al. Nov 2008 B2
7498273 Mallick et al. Mar 2009 B2
7524735 Gauri et al. Apr 2009 B1
7524750 Nemani et al. Apr 2009 B2
7541297 Mallick et al. Jun 2009 B2
7745352 Mallick et al. Jun 2010 B2
7790634 Munro et al. Sep 2010 B2
7803722 Liang Sep 2010 B2
7825038 Ingle et al. Nov 2010 B2
7825044 Mallick et al. Nov 2010 B2
7867923 Mallick et al. Jan 2011 B2
7902080 Chen et al. Mar 2011 B2
7935643 Liang et al. May 2011 B2
7943531 Nemani et al. May 2011 B2
7989365 Park et al. Aug 2011 B2
7994019 Kweskin et al. Aug 2011 B1
8129555 Cheng et al. Mar 2012 B2
20010021595 Jang et al. Sep 2001 A1
20010029114 Vulpio et al. Oct 2001 A1
20010038919 Berry et al. Nov 2001 A1
20010054387 Frankel et al. Dec 2001 A1
20020048969 Suzuki et al. Apr 2002 A1
20020081817 Bhakta et al. Jun 2002 A1
20020127350 Ishikawa et al. Sep 2002 A1
20020142585 Mandal Oct 2002 A1
20020146879 Fu et al. Oct 2002 A1
20020164891 Gates et al. Nov 2002 A1
20030040199 Agarwal Feb 2003 A1
20030064154 Laxman et al. Apr 2003 A1
20030118748 Kumagai et al. Jun 2003 A1
20030124873 Xing et al. Jul 2003 A1
20030143841 Yang et al. Jul 2003 A1
20030159656 Tan et al. Aug 2003 A1
20030172872 Thakur et al. Sep 2003 A1
20030199151 Ho et al. Oct 2003 A1
20030232495 Moghadam et al. Dec 2003 A1
20040008334 Sreenivasan et al. Jan 2004 A1
20040020601 Zhao et al. Feb 2004 A1
20040048492 Ishikawa et al. Mar 2004 A1
20040065253 Pois et al. Apr 2004 A1
20040079118 M'Saad et al. Apr 2004 A1
20040146661 Kapoor et al. Jul 2004 A1
20040152342 Li et al. Aug 2004 A1
20040161899 Luo et al. Aug 2004 A1
20040175501 Lukas et al. Sep 2004 A1
20040180557 Park et al. Sep 2004 A1
20040185641 Tanabe et al. Sep 2004 A1
20040219780 Ohuchi Nov 2004 A1
20040231590 Ovshinsky Nov 2004 A1
20040241342 Karim et al. Dec 2004 A1
20050001556 Hoffman et al. Jan 2005 A1
20050019494 Moghadam et al. Jan 2005 A1
20050026443 Goo et al. Feb 2005 A1
20050062165 Saenger et al. Mar 2005 A1
20050087140 Yuda et al. Apr 2005 A1
20050118794 Babayan et al. Jun 2005 A1
20050142895 Ingle et al. Jun 2005 A1
20050153574 Mandal Jul 2005 A1
20050181555 Haukka et al. Aug 2005 A1
20050186731 Derderian et al. Aug 2005 A1
20050186789 Agarwal Aug 2005 A1
20050196533 Hasebe et al. Sep 2005 A1
20050227499 Park et al. Oct 2005 A1
20050250340 Chen et al. Nov 2005 A1
20050260347 Narwankar et al. Nov 2005 A1
20060011984 Curie Jan 2006 A1
20060014399 Joe Jan 2006 A1
20060030165 Ingle et al. Feb 2006 A1
20060046506 Fukiage Mar 2006 A1
20060055004 Gates et al. Mar 2006 A1
20060068599 Baek et al. Mar 2006 A1
20060075966 Chen et al. Apr 2006 A1
20060096540 Choi May 2006 A1
20060110943 Swerts et al. May 2006 A1
20060121394 Chi Jun 2006 A1
20060162661 Jung et al. Jul 2006 A1
20060178018 Olsen Aug 2006 A1
20060223315 Yokota et al. Oct 2006 A1
20060228903 McSwiney et al. Oct 2006 A1
20060252240 Gschwandtner et al. Nov 2006 A1
20060281496 Cedraeus Dec 2006 A1
20060286776 Ranish et al. Dec 2006 A1
20070020392 Kobrin et al. Jan 2007 A1
20070026689 Nakata et al. Feb 2007 A1
20070031598 Okuyama et al. Feb 2007 A1
20070049044 Marsh Mar 2007 A1
20070077777 Gumpher Apr 2007 A1
20070092661 Ryuzaki et al. Apr 2007 A1
20070128864 Ma et al. Jun 2007 A1
20070134433 Dussarrat et al. Jun 2007 A1
20070166892 Hori Jul 2007 A1
20070173073 Weber Jul 2007 A1
20070181966 Watatani et al. Aug 2007 A1
20070232071 Balseanu et al. Oct 2007 A1
20070232082 Balseanu et al. Oct 2007 A1
20070275569 Moghadam et al. Nov 2007 A1
20070281495 Mallick et al. Dec 2007 A1
20070281496 Ingle et al. Dec 2007 A1
20080000423 Fukiage Jan 2008 A1
20080085607 Yu et al. Apr 2008 A1
20080102223 Wagner et al. May 2008 A1
20080102650 Adams et al. May 2008 A1
20080188087 Chen et al. Aug 2008 A1
20080206954 Choi et al. Aug 2008 A1
20080260969 Dussarrat et al. Oct 2008 A1
20080318429 Ozawa et al. Dec 2008 A1
20090035917 Ahn et al. Feb 2009 A1
20090053901 Goto et al. Feb 2009 A1
20090061647 Mallick et al. Mar 2009 A1
20090075490 Dussarrat Mar 2009 A1
20090104755 Mallick et al. Apr 2009 A1
20090104790 Liang Apr 2009 A1
20090203225 Gates et al. Aug 2009 A1
20090232985 Dussarrat et al. Sep 2009 A1
20090325391 De Vusser et al. Dec 2009 A1
20100041243 Cheng et al. Feb 2010 A1
20100221925 Lee et al. Sep 2010 A1
20110014798 Mallick et al. Jan 2011 A1
20110034035 Liang et al. Feb 2011 A1
20110034039 Liang et al. Feb 2011 A1
20110045676 Park et al. Feb 2011 A1
20110111137 Liang et al. May 2011 A1
20110129616 Ingle et al. Jun 2011 A1
20110136347 Kovarsky et al. Jun 2011 A1
20110223774 Kweskin et al. Sep 2011 A1
20120009802 LaVoie et al. Jan 2012 A1
20120111831 Ha May 2012 A1
Foreign Referenced Citations (13)
Number Date Country
19654737 Mar 1997 DE
0892083 Jan 1999 EP
1717848 Feb 2006 EP
01241826 Sep 1989 JP
10-2004-0091978 Nov 2004 KR
10-2005-0003758 Jan 2005 KR
10-2005-0094183 Sep 2005 KR
WO 02077320 Oct 2002 WO
WO 03066933 Aug 2003 WO
WO 2005078784 Aug 2005 WO
WO 2007040856 Apr 2007 WO
WO 2007140376 Dec 2007 WO
WO 2007140424 Dec 2007 WO
Related Publications (1)
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20110223774 A1 Sep 2011 US
Provisional Applications (1)
Number Date Country
61311949 Mar 2010 US