The present invention relates generally to a method of plasma processing a substrate, and, in particular embodiments, to a method of fabricating high aspect ratio (HAR) features.
Generally, a semiconductor device, such as an integrated circuit (IC) is fabricated by sequentially depositing and patterning layers of dielectric, conductive, and semiconductor materials over a substrate to form a network of electronic components and interconnect elements (e.g., transistors, resistors, capacitors, metal lines, contacts, and vias) integrated in a monolithic structure. Many of the processing steps used to form the constituent structures of semiconductor devices are performed using plasma processes.
The semiconductor industry has repeatedly reduced the minimum feature sizes in semiconductor devices to a few nanometers to increase the packing density of components. Accordingly, the semiconductor industry increasingly demands plasma processing technology to provide processes for patterning features with accuracy, precision, and profile control, often at atomic scale dimensions. Meeting this challenge along with the uniformity and repeatability needed for high volume IC manufacturing requires further innovations of plasma processing technology.
In accordance with an embodiment of the present invention, a method of processing a substrate includes while flowing a first unsaturated fluorocarbon, a saturated fluorocarbon, a first noble gas, and dioxygen into a plasma chamber, generating a plasma in the plasma chamber; and patterning, with the plasma, a material layer on the substrate.
In accordance with an embodiment of the present invention, a method of processing a substrate that includes: flowing, into a plasma chamber, dioxygen (O2), a first fluorocarbon, and a second fluorocarbon, the first fluorocarbon being unsaturated and the second fluorocarbon being saturated; flowing, into the plasma chamber, a first noble gas and a second noble gas; generating a plasma in the plasma chamber from O2, the first fluorocarbon, and the second fluorocarbon while flowing the first noble gas and the second noble gas; and etching, with the plasma, a material layer of the substrate using a patterned hardmask layer formed over the material layer as an etch mask.
In accordance with an embodiment of the present invention, a method of forming a high-aspect ratio (HAR) feature on a substrate in a plasma processing chamber, the method including: depositing an amorphous carbon layer (ACL) hardmask over a material layer including silicon oxide formed over the substrate, the substrate including silicon; patterning the ACL hardmask; flowing C3F8, C4F6, Ar, Kr, and O2 to the plasma processing chamber; generating a plasma including C3F8 and C4F6 in the plasma processing chamber while flowing the Ar, Kr, and O2; and selectively etching the material layer relative to the ACL hardmask and the substrate by exposing the substrate in the plasma processing chamber to the plasma to form the HAR feature.
For a more complete understanding of the present invention, and the advantages thereof, reference is now made to the following descriptions taken in conjunction with the accompanying drawings, in which:
This application relates to fabrication of semiconductor devices, for example, integrated circuits comprising semiconductor devices, and more particularly to high capacity three-dimensional (3D) memory devices, such as a 3D-NAND (or vertical-NAND), 3D-NOR, or dynamic random access memory (DRAM) device. The fabrication of such devices may generally require forming conformal, high aspect ratio (HAR) features (e.g., a contact hole) of a circuit element. Features with aspect ratio (ratio of height of the feature to the width of the feature) higher than 50:1 are generally considered to be high aspect ratio features, and in some cases fabricating a higher aspect ratio such as 100:1 may be desired for advanced 3D semiconductor devices. However, conventional HAR etch methods may usually comprise tens and sometimes hundreds of processing steps, which thereby complicates the process optimization and etch throughput. A simple yet effective HAR process may therefore be desired. Embodiments of the present application disclose methods of fabricating HAR features by a plasma etch process based on a combination of fluorocarbons comprising an unsaturated fluorocarbon and a saturated fluorocarbon. Further, a combination of noble gases may also be included in the plasma etch process for better etch performance.
The methods of plasma etch described in this disclosure may overcome various challenges posed for plasma etching processes for HAR features. In various embodiments, the plasma etch process may advantageously achieve a high AR equal to or higher than 100:1 with a good selectivity to a hardmask. Further, having a good etch rate, this plasma etch process may advantageously be performed in a single step with a shorter process time than a conventional HAR etch method. This feature may improve wafer throughput and the process may be cost-effective. In addition, by tuning the parameters for the additional gases, various methods described in this disclosure may also achieve maintaining the critical dimension (CD) of the hardmask opening and producing straight sidewall profile throughout the whole HAR features.
In the following,
In one or more embodiments, the substrate 100 may be a silicon wafer, or a silicon-on-insulator (SOI) wafer. In certain embodiments, the substrate may comprise a silicon germanium wafer, silicon carbide wafer, gallium arsenide wafer, gallium nitride wafer and other compound semiconductors. In other embodiments, the substrate comprises heterogeneous layers such as silicon germanium on silicon, gallium nitride on silicon, silicon carbon on silicon, as well layers of silicon on a silicon or SOI substrate.
In various embodiments, the substrate 100 is a part of a semiconductor device, and may have undergone a number of steps of processing following, for example, a conventional process. For example, the semiconductor structure may comprise a substrate 100 in which various device regions are formed. At this stage, the substrate 100 may include isolation regions such as shallow trench isolation (STI) regions as well as other regions formed therein.
The material layer 110 may be formed over the substrate 100. In various embodiments, the material layer 110 is a target layer that is to be patterned into one or more high aspect ratio (HAR) features. In certain embodiments, the HAR feature being etched into the material layer 110 may be a contact hole, slit, or other suitable structures comprising a recess. In one embodiment, the material layer 110 may be a silicon oxide layer. The material layer 110 may be deposited using an appropriate technique such as vapor deposition including chemical vapor deposition (CVD), physical vapor deposition (PVD), atomic layer deposition (ALD), as well as other plasma processes such as plasma enhanced CVD (PECVD) and other processes. In one embodiment, the material layer 110 has a thickness between 1 μm and 10 μm.
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The patterned hardmask layer 120 and/or the material layer 110 may be collectively considered as a part of the substrate 100. Further, the substrate 100 may also comprise other layers. For example, for the purpose of patterning the hardmask layer, a tri-layer structure comprising a photoresist layer, SiON layer, and optical planarization layer (OPL) may be present.
Fabricating the HAR feature in the material layer 110 may be performed by a plasma etch process using a combination of gases in accordance with various embodiments. Specifically, two fluorocarbon gases may be used. In various embodiments, the first fluorocarbon may be a unsaturated fluorocarbon and the second fluorocarbon may be a saturated fluorocarbon. In this disclosure, an unsaturated fluorocarbon refers to any compound comprising carbon and fluorine with at least one carbon-carbon double bond (C═C bond) or triple bond (C≡C bond), and a saturated fluorocarbon refers to any compound comprising carbon and fluorine without any C═C bond or C≡C bond. In certain embodiments, the unsaturated fluorocarbon may comprise hexafluorobutadiene (C4F6), hexafluoro-2-butyne (C4F6), or hexafluorocyclobutene (C4F6), and the saturated fluorocarbon may comprise octafluoropropane (C3F8), perfluorobutane (C4F10), or perflenapent (C5F12). As described more in detail below referring to
In alternate embodiments, the combination of gases may further comprise a third fluorocarbon. In one embodiment, the third fluorocarbon may be octafluorocyclobutane (C4F8), octafluoro-2-butene (C4F8), hexafluoropropylene (C3F6), carbon tetrafluoride (CF4), or fluoroform (CHF3).
Further improvement of the plasma etch process, yet in key process performance metrics other than sidewall passivation, may be achieved by adding a second noble gas in accordance with various embodiments. The second noble gas may be heavier than the first noble gas. Accordingly, the first and second noble gases may be selected from a group of helium (He), neon (Ne), argon (Ar), krypton (Kr), xenon (Xe), and radon (Rn). In certain embodiments, the first noble gas is argon and the second noble gas is krypton. The inventors of this application identified that adding a heavier second noble gas can have a dramatic difference during the etching resulting in improved etch selectivity and critical dimension uniformity (CDU) as further described below referring
Accordingly, the combination of an unsaturated fluorocarbon and a saturated fluorocarbon and the combination of two noble gases may be employed at the same time in various embodiments to optimize the overall plasma etch performance. In certain embodiments, the plasma etch process may use a combination of gases comprising C4F6, C3F8, Ar, Kr, and O2. The two combinations can advantageously improve different metrics of process performance, and thereby optimizing the process may be performed by independently tuning each of the combinations as well as a parameter for a balancing agent.
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In certain embodiments, the addition of the balancing agent such as dioxygen (O2) may also be beneficial in this aspect of controlling the amount of deposition. For example, dissociated oxygen species may help controlling the amount of the top deposition 130B, particularly near the openings 126. As a result, clogging may be prevented while the etchants and sidewall passivation species may reach into the recesses 125.
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Continuing the plasma etch process, the recesses 125 illustrated in
In various embodiments, a RF pulsing at a kHz range may be used to power the plasma. Using the RF pulsing may help generating high energetic ions (>keV) in the plasma for the plasma etch process, while reducing a charging effect. The charging effect during a process is a phenomenon where electrons build charge on insulating materials (e.g., silicon oxide of the materials layer 110) creating a local electric field that may steer positive ions to the sidewalls and cause a lateral etching. Therefore, fine tuning the power conditions of the plasma etch process may also be important to minimize the widening of critical dimension (CD) of the high aspect ratio (HAR) feature. In certain embodiments, a moderate duty ratio between 40% to 80% may be used. In one embodiment, a bias power of 18 kW may be pulsed at a frequency of 5 kHz with a duty ratio of 60%.
In certain embodiments, where C4F6 and C3F8 are included as the fluorocarbon in the plasma etch process, the C3F8:C4F6 ratio may be kept within the range of 2:1 to 0.2:1.
In certain embodiments, where argon (Ar) and krypton (Kr) are included as the noble gases in the plasma etch process, the Kr flow rate may be 150 sccm or higher. In one embodiment, the Kr flow rate may be 50 sccm or higher at a pressure between 10 mTorr to 30 mTorr. In one embodiment, the flow rate ratio Kr:Ar may be kept within the range of 0.1:1 to 5:1, for example, between 0.5:1 to 0.95:1 in one embodiment.
In one embodiment, the plasma etch process may be performed at gas flow rates of 90-100 sccm for C4F6, 65-75 sccm for C3F8, 60-70 sccm for O2, 340-360 sccm for Ar, and 260-290 sccm for Kr, at a temperature of 10-30° C., and at a pressure of 10-30 mTorr, using a dual-frequency capacitively coupled plasma (CCP) chamber with pulsing capabilities at a high frequency (HF) power of 2000-6000 W, at a low frequency (LF) power at 10000-25000 W, at a pulsing frequency of 1-10 kHz, and at a pulsing duty ratio of 40-80%. With the example conditions above, the HAR feature with a high critical dimension uniformity (CDU) and a good sidewall passivation may be obtained (e.g.,
In certain embodiments, the plasma etch process may be advantageously performed as a continuous process with a process time of 60 min or less to form a high aspect ratio (HAR) feature with an aspect ratio of 100:1 or higher.
In one embodiment, after 30-50 min of a continuous etching process, the plasma etch process may drill through a layer of 6-8 μm silicon oxide (SiO2) with 20-30% over etch (OE) by sacrificing 1-2 μm of amorphous carbon layer (ACL) hardmask, which yields a SiO2-to-ACL selectivity between 3:1 to 5:1.
In various embodiments, process parameters may be selected to optimize the characteristics of the high aspect ratio (HAR) feature considering various factors comprising controlled level of deposition, selectivity to the hardmask, sidewall passivation in the HAR feature, and good critical dimension uniformity (CDU) among others.
Characteristics, such as CD and pattern defects of the HAR feature, may be measured using optical techniques such as scatterometry, a scanning electron microscope (SEM), transmission electron microscope (TEM), high-resolution TEM (HR-TEM), scanning probe microscope (SPM), atomic force microscope (AFM), scanning tunneling microscope (STM), or other suitable devices.
The process parameters may comprise gas selection, gas flow rates, pressure, temperature, process time, and plasma conditions such as source power, bias power, RF pulsing conditions. In certain embodiments, advantageously enabled by the combination of fluorocarbons and noble gases, some of the process parameters may be adjusted individually to tune each of the above factors (e.g., controlled level of deposition, selectivity to the hardmask, sidewall passivation in the HAR feature, and good CDU) through experiments. For example, if an existing condition cause a clogging issue, one may increase the gas flow rate of a saturated fluorocarbon such as C3F8 and/or a balancing agent such as dioxygen (O2). In another example, if the existing condition leads to a fast consumption of the hardmask (i.e., a poor selectivity to the hardmask), one may increase the gas flow rate of the unsaturated fluorocarbon such as C4F6. In a separate example, if the existing condition results in issues in CDU, one may adjust the Ar and Kr flow rate so that desired radical species and density can be produced. The effect of some of the process parameters on the etch performance are further described below referring to
Further processing may follow conventional processing, for example, by removing the patterned hardmask layer 120, sidewall deposition 130A and top deposition 130B.
When one or more of the above important factors for the plasma etch process (e.g., controlled level of deposition, selectivity to the hardmask, sidewall passivation, etc.) are absent, the plasma etch process may lead to different structures as illustrated in
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The gases may be introduced into the plasma processing chamber 510 by a gas delivery system 520. The gas delivery system 520 comprises multiple gas flow controllers to control the flow of multiple gases into the chamber. Each of the gas flow controllers of the gas delivery system 520 may be assigned for each of fluorocarbons, noble gases, and/or balancing agents. In some embodiments, optional center/edge splitters may be used to independently adjust the gas flow rates at the center and edge of the substrate 100.
The RF-bias power sources 570 and 580 may be used to supply continuous wave (CW) or pulsed RF power to sustain the plasma, such as a plasma 560. The plasma 560, shown between the top electrode 552 and the bottom electrode (also the substrate holder 554), exemplifies direct plasma generated close to the substrate 100 in the plasma processing chamber 510 of the plasma processing system 50. Etching may be performed by exposing the substrate 100 to the plasma 560 while powering the substrate holder 554 with RF-bias power sources 570, 580 and optionally the top electrode 552 with the DC power source 550.
The configuration of the plasma processing system 50 described above is by example only. In alternative embodiments, various alternative configurations may be used for the plasma processing system 50. For example, inductively coupled plasma (ICP) may be used with RF source power coupled to a planar coil over a top dielectric cover, the gas inlet and/or the gas outlet may be coupled to the upper wall, etc. In various embodiments, the RF power, chamber pressure, substrate temperature, gas flow rates and other plasma process parameters may be selected in accordance with the respective process recipe. In some embodiments, the plasma processing system 50 may be a resonator such as a helical resonator.
Although not described herein, embodiments of the present invention may be also applied to remote plasma systems as well as batch systems. For example, the substrate holder may be able to support a plurality of wafers that are spun around a central axis as they pass through different plasma zones.
Example embodiments of the invention are summarized here. Other embodiments can also be understood from the entirety of the specification as well as the claims filed herein.
Example 1. A method of processing a substrate that includes: while flowing a first unsaturated fluorocarbon, a saturated fluorocarbon, a first noble gas, and dioxygen (O2) into a plasma chamber, generating a plasma in the plasma chamber; and patterning, with the plasma, a material layer on the substrate.
Example 2. The method of example 1, where the first unsaturated fluorocarbon includes hexafluorobutadiene (C4F6), hexafluoro-2-butyne (C4F6), or hexafluorocyclobutnene (C4F6).
Example 3. The method of one of examples 1 or 2, where the saturated fluorocarbon includes octafluoropropane (C3F8), perfluorobutane (C4F10), or perflenapent (C5F12).
Example 4. The method of one of examples 1 to 3, where the material layer includes silicon oxide.
Example 5. The method of one of examples 1 to 4, further including, while flowing the first noble gas, flowing a second noble gas that is heavier than the first noble gas.
Example 6. The method of one of examples 1 to 5, where a ratio of a gas flow rate of the first unsaturated fluorocarbon to a gas flow rate of the saturated fluorocarbon is between 2:1 to 0.2:1
Example 7. The method of one of examples 1 to 6, further including flowing a third fluorocarbon.
Example 8. A method of processing a substrate that includes: flowing, into a plasma chamber, dioxygen (O2), a first fluorocarbon, and a second fluorocarbon, the first fluorocarbon being unsaturated and the second fluorocarbon being saturated; flowing, into the plasma chamber, a first noble gas and a second noble gas; generating a plasma in the plasma chamber from O2, the first fluorocarbon, and the second fluorocarbon while flowing the first noble gas and the second noble gas; and etching, with the plasma, a material layer of the substrate using a patterned hardmask layer formed over the material layer as an etch mask.
Example 9. The method of example 8, where the material layer includes silicon oxide, and where the patterned hardmask layer includes amorphous carbon layer (ACL).
Example 10. The method of one of examples 8 or 9, where the first noble gas is argon (Ar), and where the second noble gas is krypton (Kr).
Example 11. The method of one of examples 8 to 10, where the first fluorocarbon includes a fluorocarbon with a chemical formula of C4F6, and where the second fluorocarbon includes a fluorocarbon with a chemical formula of C3F8.
Example 12. The method of example 10, a gas flow rate of Kr is 50 sccm or greater.
Example 13. A method of forming a high-aspect ratio (HAR) feature on a substrate in a plasma processing chamber, the method including: depositing an amorphous carbon layer (ACL) hardmask over a material layer including silicon oxide formed over the substrate, the substrate including silicon; patterning the ACL hardmask; flowing C3F8, C4F6, Ar, Kr, and O2 to the plasma processing chamber; generating a plasma including C3F8 and C4F6 in the plasma processing chamber while flowing the Ar, Kr, and O2; and selectively etching the material layer relative to the ACL hardmask and the substrate by exposing the substrate in the plasma processing chamber to the plasma to form the HAR feature.
Example 14. The method of example 13, further including applying a pulsed RF bias power to the plasma.
Example 15. The method of example 14, where the pulsed RF bias power has a duty ratio between 40% to 80%.
Example 16. The method of one of examples 13 to 15, where the HAR feature has an aspect ratio (height to width) of 100:1 or greater.
Example 17. The method of one of examples 13 to 16, where the substrate is exposed to the plasma only once.
Example 18. The method of one of examples 13 to 17, where a duration of exposing the substrate to the plasma is less than 60 min.
Example 19. The method of one of examples 13 to 18, further including: performing an intermediate process including a deposition step adding materials on the ACL hardmask and sidewalls of the HAR feature, and repeating the selectively etching and the intermediate process.
Example 20. The method of example 19, where the intermediate process further includes performing a flash step to remove clogged openings of the ACL hardmask.
While this invention has been described with reference to illustrative embodiments, this description is not intended to be construed in a limiting sense. Various modifications and combinations of the illustrative embodiments, as well as other embodiments of the invention, will be apparent to persons skilled in the art upon reference to the description. It is therefore intended that the appended claims encompass any such modifications or embodiments.