The background description provided here is for the purpose of generally presenting the context of the present disclosure. Anything described in this background section, and potentially aspects of the written description, are not expressly or impliedly admitted as prior art with respect to the present application.
The present disclosure relates to the formation of semiconductor devices. More specifically, the disclosure relates etching to form semiconductor devices.
For etching silicon oxide (SiO2), a fluorine containing reactive ion etch may be use. If a reactive ion etch process uses a mask that is too thick, etch resolution is decreased. Some etch processes are not sufficiently selective requiring thicker etch masks.
To achieve the foregoing and in accordance with the purpose of the present disclosure, a method for forming etched features in a layer of a first material is provided. A layer of a second material is deposited over the layer of the first material. An alloy layer of the first material and the second material is formed between the layer of the first material and the layer of the second material. The layer of the first material is selectively etched with respect to the alloy layer, using the alloy layer as a hardmask.
In another manifestation, a method for etching a layer of a first material is provided. The method comprises a plurality of cycles, wherein each cycle, comprises depositing a layer of a second material over the layer of the first material, forming an alloy layer of the first material and the second material between the layer of the first material and the layer of the second material. etching away the layer of the second material, and etching away the alloy layer.
In another manifestation, a method for forming an alloy layer with features is provided. An alloy layer is deposited comprising a plurality of cycles, wherein each cycle comprises depositing by atomic layer deposition a layer of a first material and depositing by atomic layer deposition a layer of a second material, wherein the layer of the first material and the layer of the second material form the alloy layer.
These and other features of the present disclosure will be described in more detail below in the detailed description of the disclosure and in conjunction with the following figures.
The present disclosure is illustrated by way of example, and not by way of limitation, in the figures of the accompanying drawings and in which like reference numerals refer to similar elements and in which:
The present disclosure will now be described in detail with reference to a few preferred embodiments thereof as illustrated in the accompanying drawings. In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present disclosure. It will be apparent, however, to one skilled in the art, that the present disclosure may be practiced without some or all of these specific details. In other instances, well-known process steps and/or structures have not been described in detail in order to not unnecessarily obscure the present disclosure.
For etching silicon oxide (SiO2), a fluorine containing reactive ion etch may be use. If a reactive ion etch process uses a mask that is too thick, etch resolution is decreased. Some etch processes are not sufficiently selective requiring thicker etch masks. One method of improving an etch process is by providing a hardmask that allows a material to be highly selectively etched with respect to the hardmask. An embodiment provides a method for depositing a thin hardmask that allows a substrate, such as SiO2 to be highly selectively etched with respect to the hardmask.
In order to facilitate understanding of an embodiment,
A patterned mask is deposited on the first material layer 208 (step 108). In this example, a patterned mask is formed on the first material layer 208. The patterned mask may be any possible material deposited by any possible manner at any possible thickness. In an embodiment, the patterned mask may be formed by depositing a layer of a mask material and then forming features in the mask material. The patterned mask may be formed by other methods. The patterned mask 209 may be a photoresist mask.
A second material is deposited over the first material layer 208 and the patterned mask 209 (step 112). The second material may be any possible material deposited in any possible manner at any possible thickness.
An alloy layer is formed between the first material layer 208 and the second material layer 212 (step 116). In the specification and claims, an alloy is defined as a material of a mixture comprising a first metal and at least one of a second metal different from the first metal, silicon and carbon. This process may use any possible alloy forming process. In this embodiment, heat is used to form an alloy layer between the first material layer 208 and the second material layer 212. In other embodiments, the first material layer 208 and the second material layer 212 form an alloy without the addition of heat.
Since in this embodiment some unalloyed second material layer 212 remains, the unalloyed second material is etched away (step 120). Any process that is able to selectively etch the unalloyed second material may be used. In this example, a hydrogen-based etch is used. In this example, a second material etch gas of hydrogen (H2) is provided. The second material etch gas is formed into a plasma that etches the second material with respect to the alloy layer 216.
The patterned mask 209 is removed (step 124). Any process for selectively removing the patterned mask 209 may be used. In this example, an oxygen containing plasma is used to strip the patterned mask 209.
The first material is etched with respect to the alloy layer 216 (step 128). Any process that is able to selectively etch the first material with respect to the alloy layer 216 may be used. The patterned alloy layer 216 is used as a hardmask for etching the first material layer 208. In this example, a first etch gas of carbon tetrafluoride (CF4) or another fluorocarbon-based etch gas is used.
Using the alloy layer 216 as a hardmask may allow for an increased etch selectivity for etching the first material layer 208 with respect to the hardmask of the alloy layer 216. The higher selectivity may allow for a thinner hardmask alloy layer 216. In addition, if the second material layer 212 is deposited by atomic layer deposition or chemical vapor deposition, the second layer may be deposited as a thin conformal layer. Since the resulting alloy layer 216 is formed from the second material layer 212, the resulting alloy layer 216 may also be thin and conformal. Therefore, this embodiment may use the alloy layer 216 to provide a thinner and more conformal hardmask that may provide a highly selective etch of the first material with respect to the hardmask. In some embodiments, the substrate 204 may be etched using either the first material layer 208 or the alloy layer 216 as a mask (step 132).
In various embodiments, if the first material layer 208 is SiO2, then the second material layer 212 may be at least one of tin (Sn), aluminum (Al), boron (B), molybdenum (Mo), platinum (Pt), and tungsten (W). In such embodiments, a halogen containing recipe may be used to selectively etch the SiO2 first material layer 208.
In other embodiments, if the first material layer 208 is silicon Si or silicon carbide (SiC), then the second material layer 212 may be at least one of tin (Sn), aluminum (Al), boron (B), molybdenum (Mo), and tungsten (W).
In other embodiments, the first material layer comprises a metal containing material. For example, the metal containing material may comprise titanium nitride (TiN), tantalum nitride (TaN), aluminum nitride (AlN), and tungsten nitride (WNx). In various embodiments, the second material layer comprises, Si, germanium (Ge), and tin (Sn).
In various embodiments, the first material layer 208 is made of a carbon containing material. In such embodiments, the second layer may comprise tin (Sn), Aluminum (Al), Boron (B), Molybdenum (Mo), and tungsten (W).
In another embodiment, the alloy layer may be used as a type of an atomic layer etch.
An alloy layer is formed between the first material layer 408 and the second material layer 412 (step 308). In this embodiment, the deposition of the first material layer 408 automatically forms the alloy layer.
Since in this embodiment some unalloyed second material layer 412 remains, the second material layer 412 is etched away (step 312). The alloy layer 416 is removed (step 316). Many possible processes may be used to remove the second material layer 412 and the alloy layer 416 in various embodiments. In this embodiment, a single plasma etch process is used to remove both the unalloyed second material layer 412 (step 312) and to remove the alloy layer 416 (step 316). A plasma formed from a nitrogen trifluoride (NF3) gas is able to etch titanium oxide of the unalloyed second material layer 412 and etch titanium-silicon-oxide of the alloy layer 416.
In this embodiment, alloying the SiO2 with Ti, allows the Ti to breakup and change the SiO2 layer to form the titanium-silicon-oxide alloy. As a result, the titanium-silicon-oxide is able to be etched by the plasma. In other embodiments, tantalum (Ta), zirconium (Zr), or hafnium (HF) are used to breakup and change the SiO2 layer.
Since some of the first material layer 408 remains, the etch process is continued (step 320), by repeating the cyclical process by going back to the step of depositing a second material layer on the first material layer 408 (step 304). In this embodiment, the cycles are repeated until the first material layer 408 is etched away.
Using the alloy layer 416 as a selective etch layer allows for controlled etch. In addition, since the second material layer 412 is deposited by atomic layer deposition or chemical vapor deposition, the second layer is deposited as a thin conformal layer. Since the resulting alloy layer 416 is formed from the second material layer 412, the resulting alloy layer 416 is also thin and conformal. Therefore, this embodiment allows the etching of the first material layer 408 by thin conformal layers, allowing for a highly selective and conformal etch. In various embodiments, a physical etching requiring a high bias may be needed to etch the first material layer. Forming an alloy layer and then etching the alloy, may use an alloy that can be etched using a chemical etch. Such a chemical etch would use a low or no bias, improving the etch process and reducing damage caused by bombardment. As a result, the alloy layer may be used for an atomic layer etch type of etch with reduced ion bombardment.
In various embodiments, the first material layer 408 is Si or SiC. In such embodiments, the second layer may comprise at least one of Ti, Ta, Zr, nickel (Ni), and cobalt (Co).
In other embodiments, the first material layer comprises a metal containing material. For example, the metal containing material may comprise at least one of TiN, TaN, and AlN In various embodiments, the second material layer comprises at least one of W and Mo.
In various embodiments, the first material layer 208 is made of a carbon containing material. In such embodiments, the second layer may comprise at least one of Si, Ge, Sn, W, and Mo.
In some embodiments, a patterned mask may be placed over the first material layer 408 before etching the first material layer 408. The patterned mask provides a patterned etch of the first material layer 408.
In another embodiment, the alloy layer may be used to provide a selective etch to form features.
A second material is deposited on the first material (step 508). In various embodiments, the second material layer may be any material. This second materials may be deposited by any method at any thickness.
The deposition of alternating layers of the first material layer 608 and the second material layer 612 is continued (step 512) for a plurality of cycles resulting in a stack with a plurality of alternating layers of the first material layer 608 and the second material layer 612.
An alloy layer or alloy layers are formed between the first material layers 608 and the second material layers 612 (step 516). Any alloying process may be used to alloy the first material layer 608 and the second material layer 612. In this embodiment, heat is used to form an alloy layer between the first material layers 608 and the second material layers 612. In other embodiments, the first material layer 608 and second material layer 612 form an alloy without the addition of heat.
A patterned mask is formed over the alloy layer 616 (step 520). The patterned mask may be of any possible material. In this embodiment, the patterned mask is a photoresist mask comprising at least one of a polymer photoresist and a metal containing photoresist. The patterned mask may comprise an underlayer comprising at least one of carbon such as amorphous carbon, spin-on-carbon (SOC). The patterned mask may also comprise an underlayer comprising at least one of silicon containing material such as spin-on-glass (SOG), SiO2, silicon nitride (SiN), SiC, silicon oxycarbide (SiOC), and silicon oxycarbonitride (SiOCN).
The alloy layer 616 is etched (step 524). In various embodiments, one of many different etch processes may be used. In this embodiment, a plasma formed from a nitrogen trifluoride (NF3) gas is used to etch titanium oxide, but is not able to etch the titanium-tin-oxide alloy, since tin tetrafluoride (SnF4) is not volatile. A plasma formed from H2 is able to etch tin oxide, but not titanium-tin-oxide, since titanium tetrahydride (TiH4) is not stable. In one embodiment, a plasma is formed from a gas of a mixture of NF3 and H2. The ratio of the flow rate of NF3 to H2 can be tuned in order to control the etch of the alloy layer 616.
In another embodiment, an etch of the alloy may be performed as a cyclical process.
The first material is etched (step 708). Various embodiments may have different etch processes. In this embodiment, a first chemistry of a H2 gas is formed into a plasma to etch away a top layer of tin of the alloy layer 616 of titanium-tin-oxide. The first chemistry is used to selectively etch the first material with respect to the second material. The etch is self-limiting since the titanium prevents further etching of the alloy layer.
If the etch is not complete and is to be continued (step 712), then the process is repeated for another cycle.
Forming the alloy layer 616 and using the alloy layer 616 as a selective etch layer allows for controlled conformal etch. In an embodiment where the first material layer 608 and the second material layer 612 are deposited by atomic layer deposition or chemical vapor deposition, the first material layer 608 and the second material layer 612 are deposited as thin conformal layers. The first material layer 608 and the second material layer 612 are thin enough so that all of the first material layer 608 and all of the second material layer 612 are alloyed, instead of forming a nanolaminate of different material layers. Since this etch is self-limiting and etches only one atomic layer for each etch step, this process provides an atomic layer etch. Since the atomic layer etch is a chemical etch, instead of a physical etch, the resulting etch is highly conformal.
In other embodiments, the first material layer 608 and the second material layer 612 may be silicon and aluminum. Silicon oxide may be etched with a fluorine containing plasma. Aluminum oxide may be etched with a chlorine containing plasma.
In some embodiments, the first layers and the second layers may form nanolaminates of different layers. In other embodiments, the ratios of concentrations or thicknesses of the first material and the second material may be varied at different heights.
Uniform depositions that do not vary in thickness provide more uniform alloying. Thickness variations cause chemical variations. Since atomic layer deposition provides layers of uniform thickness, atomic layer deposition, would be preferred in some embodiments in the formation of thin uniform layers.
While this disclosure has been described in terms of several preferred embodiments, there are alterations, modifications, permutations, and various substitute equivalents, which fall within the scope of this disclosure. It should also be noted that there are many alternative ways of implementing the methods and apparatuses of the present disclosure. It is therefore intended that the following appended claims be interpreted as including all such alterations, modifications, permutations, and various substitute equivalents as fall within the true spirit and scope of the present disclosure.
This application claims the benefit of priority of U.S. Application No. 62/968,400, filed Jan. 31, 2020, which is incorporated herein by reference for all purposes.
Filing Document | Filing Date | Country | Kind |
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PCT/US2021/014938 | 1/25/2021 | WO |
Number | Date | Country | |
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62968400 | Jan 2020 | US |