A method for fabricating a p-type silicon carbide device structure and a method for fabricating a silicon carbide device
By forming an aluminum-silicon mixed solution in a vacuum high-temperature CVD furnace and introducing a carbon source gas, a p-type silicon carbide layer is prepared, which solves the high cost and quality problems in the existing technology and achieves the effects of simplifying the process and improving device performance.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- ZJU HANGZHOU GLOBAL SCI & TECH INNOVATION CENT
- Filing Date
- 2026-04-01
- Publication Date
- 2026-06-23
AI Technical Summary
Existing technologies for fabricating p-type silicon carbide devices suffer from high costs, uneven photoresist coating, low etching rates, and severe etching damage, leading to reduced device yield and performance degradation.
The semiconductor substrate is heated in a vacuum high-temperature CVD furnace to form an aluminum-silicon mixed solution. A carbon source gas is introduced and pyrolyzes on the surface of the aluminum-silicon mixed solution to form a p-type silicon carbide layer. Residual reactants are removed by cleaning. The process can be simplified into three main steps.
It greatly simplifies the process flow, reduces costs, avoids quality problems caused by photoresist and etching, and improves device yield and performance.
Smart Images
Figure CN121969031B_ABST
Abstract
Description
Technical Field
[0001] This invention relates to the field of semiconductor device technology, and in particular to a method for fabricating a p-type silicon carbide device structure and a method for fabricating silicon carbide devices. Background Technology
[0002] In the final stage of fabrication of grooved silicon carbide devices (such as trench gate MOSFETs and grooved PIN diodes), a P-type silicon carbide groove layer is typically added. The purpose is to achieve low contact resistance, efficient carrier injection, and enhanced device reliability without increasing additional losses.
[0003] Traditional processes for preparing p-type silicon carbide trench layers are described in [link to documentation]. Figure 1 As shown, the process typically involves epitaxy, photolithography, etching, and cleaning. First, epitaxy, photolithography, and etching are all high-cost processes that significantly increase device manufacturing costs. Second, during photolithography, due to the strong chemical inertness and low surface energy of silicon carbide, high-contrast photoresists adapted for SiC are not yet in mass production. Conventional photoresists are difficult to spread evenly and adhere firmly, leading to defects such as pinholes, lifting, and edge shrinkage after coating.
[0004] Secondly, photoresist removal is difficult. Whether it is wet cleaning or high-temperature removal, both will increase the risk of device leakage current and add an additional 10%-15% yield loss.
[0005] During the etching process, due to the Si-C bond energy of silicon carbide reaching 710 kJ / mol, the conventional etching rate is only 0.5-1 μm / h, exhibiting characteristics such as low etching rate. On the other hand, conventional etching can also lead to severe etching damage to silicon carbide materials.
[0006] Furthermore, even with doping methods such as ion implantation, high-energy ion bombardment can create amorphous layers, vacancies, and dislocation defects on the silicon carbide surface. These defects become carrier recombination centers, leading to a 10%-20% decrease in device breakdown voltage and a reduction in carrier mobility of over 30%. Although annealing can repair some of the damage, it requires temperatures above 1600°C, which can trigger substrate sublimation and dopant diffusion, further reducing yield. Summary of the Invention
[0007] To address the problems of traditional processes, the present invention aims to provide a simpler and lower-cost method for fabricating p-type silicon carbide device structures; another objective of the present invention is to provide a method for fabricating silicon carbide devices.
[0008] This invention discloses a method for fabricating a p-type silicon carbide device structure, comprising:
[0009] A semiconductor substrate is provided, and a silicon layer and an aluminum layer are sequentially formed on a predetermined area on the surface of the semiconductor substrate using a mask;
[0010] The semiconductor substrate with silicon and aluminum layers is heated in a vacuum high-temperature CVD furnace until the aluminum layer melts and the silicon in the silicon layer dissolves in the molten aluminum, forming an aluminum-silicon mixed solution layer in a predetermined area on the surface of the semiconductor substrate. A carbon source gas is then introduced, and the carbon source gas decomposes upon contact with the hot aluminum-silicon mixed solution. Carbon atoms in the carbon source gas dissolve into the aluminum-silicon mixed solution and diffuse, reacting with the silicon in the aluminum-silicon mixed solution to form silicon carbide on the surface of the predetermined area on the semiconductor substrate. The aluminum in the aluminum-silicon mixed solution replaces the silicon in the silicon carbide, thereby forming a p-type silicon carbide layer.
[0011] The temperature of the semiconductor substrate is lowered to room temperature, and the residual reactants on the surface of the p-type silicon carbide layer are removed by a cleaning process, thereby forming a p-type silicon carbide layer on the surface of a predetermined region of the semiconductor substrate.
[0012] Furthermore, the step of sequentially forming a silicon layer and an aluminum layer on a predetermined area of the semiconductor substrate surface using a mask includes:
[0013] A metal mask is formed on the surface of the semiconductor substrate, the metal mask having an opening that exposes a predetermined area; a silicon layer and an aluminum layer are sequentially formed on the surface of the semiconductor substrate; the metal mask is removed, and stacked and discrete silicon and aluminum layers are formed in the predetermined area on the surface of the semiconductor substrate.
[0014] Furthermore, the method for sequentially forming the silicon layer and the aluminum layer includes at least one of magnetron sputtering, electron beam evaporation, and thermal evaporation.
[0015] Furthermore, the thickness ratio of the silicon layer to the aluminum layer is less than 1:10.
[0016] Furthermore, the ratio of the thickness of the p-type silicon carbide layer to the length-to-width ratio of each p-type silicon carbide layer is less than 1:10.
[0017] Furthermore, the specific process of placing the semiconductor substrate with the silicon and aluminum layers in a vacuum high-temperature CVD furnace includes:
[0018] The semiconductor substrate with silicon and aluminum layers formed is placed in a high-temperature CVD furnace and evacuated to 10°C. -5Pa, argon gas is introduced and heated to 1000-1800℃ until the aluminum layer melts. The silicon in the silicon layer dissolves in the molten aluminum, forming an aluminum-silicon mixed solution layer in a predetermined area on the surface of the semiconductor substrate. A mixture of carbon source gas and argon gas is introduced. The carbon source gas decomposes upon contact with the hot aluminum-silicon mixed solution surface. Carbon atoms in the carbon source gas dissolve into the aluminum-silicon mixed solution and diffuse, reacting with the silicon in the aluminum-silicon mixed solution to form silicon carbide on the surface of the predetermined area on the semiconductor substrate. The aluminum in the aluminum-silicon mixed solution replaces the silicon in the silicon carbide, thereby forming a p-type silicon carbide layer.
[0019] Furthermore, the flow rate ratio of carbon source gas to argon in the mixed gas is 4:50, and the carbon source gas includes at least one of methane, ethylene, propane, propylene, butane, and butene.
[0020] Furthermore, the cleaning process includes using a cleaning solution to remove residual reactants from the surface of the p-type silicon carbide layer; the cleaning solution is a strong acid cleaning solution.
[0021] Furthermore, the semiconductor substrate is a silicon carbide wafer, a silicon wafer with a silicon carbide epitaxial layer on its surface, or a silicon wafer.
[0022] This invention also discloses a method for fabricating a silicon carbide device, comprising:
[0023] A p-type silicon carbide layer is formed on the surface of a predetermined region of the semiconductor substrate using the fabrication method of the p-type silicon carbide device structure described above;
[0024] A silicon carbide device is formed on the surface of the p-type silicon carbide layer.
[0025] In summary, the advantages and beneficial effects of the present invention are as follows:
[0026] This invention provides a method for fabricating a p-type silicon carbide device structure. First, a silicon layer and an aluminum layer are sequentially formed on a semiconductor substrate. Then, a p-type doped silicon carbide surface is grown on the substrate with the aluminum and silicon layers using a vapor-liquid-solid (VLS) growth mechanism. Finally, the surface is cleaned to remove unreacted impurities. Compared with traditional fabrication methods, this method requires only three steps, greatly simplifying the process, reducing costs, and avoiding the quality problems associated with photoresist, etching, or ion implantation in p-type silicon carbide devices. Attached Figure Description
[0027] Figure 1 A schematic diagram of the process used to fabricate p-type silicon carbide device structures using existing technologies;
[0028] Figure 2 A schematic flowchart illustrating a method for fabricating a p-type silicon carbide device structure according to an embodiment of the present invention;
[0029] Figure 3 This is a schematic diagram of a semiconductor substrate structure provided in an embodiment of the present invention;
[0030] Figure 4 This is a schematic diagram of the structure after a silicon layer and an aluminum layer are sequentially formed in a predetermined area on the surface of a semiconductor substrate, according to an embodiment of the present invention.
[0031] Figure 5 This is a schematic diagram of the structure after a p-type silicon carbide layer is formed on a predetermined region of the semiconductor substrate according to an embodiment of the present invention;
[0032] Figure 6 This is a schematic diagram of the structure after residual reactants on the surface of the p-type silicon carbide layer of a semiconductor substrate are removed using a cleaning process according to an embodiment of the present invention.
[0033] Explanation of the labels in the attached diagram:
[0034] 10. Semiconductor substrate; 20. Silicon layer; 30. Aluminum layer; 40. p-type silicon carbide layer; 50. Residual reactants. Detailed Implementation
[0035] To make the objectives, technical solutions, and advantages of this invention clearer, the technical solutions of this invention will be clearly and completely described below in conjunction with specific embodiments and corresponding drawings. Obviously, the described embodiments are only a part of the embodiments of this invention, and not all of them. Based on the embodiments of this invention, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of this invention.
[0036] Embodiments of the present invention are described in detail below. Examples of these embodiments are shown in the accompanying drawings, wherein the same or similar reference numerals denote the same or similar elements or elements having the same or similar functions throughout. The embodiments described below with reference to the accompanying drawings are exemplary and are only used to explain the present invention, and should not be construed as limiting the present invention.
[0037] like Figure 2 As shown, Figure 2 The flowchart of a method for fabricating a p-type silicon carbide device structure provided in an embodiment of the present invention is shown, specifically including steps S10-S30.
[0038] S10. A semiconductor substrate 10 is provided, and a silicon layer 20 and an aluminum layer 30 are sequentially formed on a predetermined area on the surface of the semiconductor substrate 10 using a mask.
[0039] S20. The semiconductor substrate 10, on which the silicon layer 20 and the aluminum layer 30 are formed, is placed in a vacuum high-temperature CVD furnace and heated until the aluminum layer 30 melts and the silicon in the silicon layer 20 dissolves in the molten aluminum, forming an aluminum-silicon mixed solution layer in a predetermined area on the surface of the semiconductor substrate 10. A carbon source gas is introduced, and the carbon source gas decomposes upon contact with the surface of the hot aluminum-silicon mixed solution. The carbon atoms in the carbon source gas dissolve into the aluminum-silicon mixed solution and diffuse, reacting with the silicon in the aluminum-silicon mixed solution to form silicon carbide on the surface of the predetermined area on the surface of the semiconductor substrate 10. The aluminum in the aluminum-silicon mixed solution replaces the silicon in the silicon carbide, thereby forming a p-type silicon carbide layer 40.
[0040] S30. The temperature of the semiconductor substrate 10 is reduced to room temperature, and the residual reactants 50 on the surface of the p-type silicon carbide layer 40 are removed by a cleaning process, thereby forming a p-type silicon carbide layer 40 on the surface of a predetermined region of the semiconductor substrate 10.
[0041] In one embodiment, such as Figures 3-4 As shown, in step S10, the sequential formation of a silicon layer 20 and an aluminum layer 30 on a predetermined area of the semiconductor substrate surface using a mask includes:
[0042] A metal mask is formed on the surface of a semiconductor substrate 10, the metal mask having an opening that exposes a predetermined area; a silicon layer 20 and an aluminum layer 30 are sequentially formed on the surface of the semiconductor substrate 10; the metal mask is removed, and stacked and discrete silicon layers 20 and aluminum layers 30 are formed in a predetermined area on the surface of the semiconductor substrate 10.
[0043] Specifically, the semiconductor substrate 10 is a silicon carbide wafer, a silicon wafer with a silicon carbide epitaxial layer on its surface, or a silicon wafer. The semiconductor substrate 10 may or may not have other devices or other semiconductor structures formed on it.
[0044] Specifically, the method for sequentially forming the silicon layer 20 and the aluminum layer 30 includes at least one of magnetron sputtering, electron beam evaporation, and thermal evaporation.
[0045] In this embodiment, magnetron sputtering is used to achieve ultra-thin and ultra-precise ratio control of silicon (a few nanometers) and aluminum (tens of nanometers), with an extreme precision down to the thickness ratio of silicon layer 20 to aluminum layer 30 (<1:10). This allows the Al / Si thin film to serve as a precise "raw material" for subsequent reactions and doping. The thin film formed by high-kinetic-energy atoms in magnetron sputtering is dense and has extremely strong adhesion. During subsequent heating, the film is less prone to agglomeration and spheroidization, and can stably form the desired Al-Si eutectic droplets.
[0046] Specifically, the thickness ratio of the formed silicon layer 20 to the aluminum layer 30 is less than 1:10.
[0047] The amount of aluminum doping in the subsequent gas-liquid-solid (VLS) reaction can be adjusted by regulating the thickness ratio of silicon layer 20 to aluminum layer 30. The VLS growth mechanism requires a liquid metal catalyst droplet to absorb and transport carbon from the gas source, precipitating SiC on the substrate surface. In this process, aluminum is the primary solvent (catalyst). When the subsequent heating temperature exceeds the Al-Si eutectic point (approximately 577°C), the aluminum melts and dissolves the underlying thin silicon layer, forming an Al-Si alloy droplet. If silicon layer 20 is too thick (with a ratio close to or greater than 1:1), the silicon content is too high, far exceeding the solid solubility of Si in the aluminum solution. The silicon cannot be completely dissolved in the aluminum solution, making it difficult to maintain ideal liquid flow at the set process temperature. Simultaneously, the properties of the alloy solution change, and the diffusion ability of carbon in the alloy solution is also affected, ultimately causing the growth process to deviate from the optimal growth window.
[0048] Therefore, the thickness ratio of silicon layer 20 to aluminum layer 30 is less than 1:10, which ensures that Al is the absolute dominant component in the droplet, while silicon is only a small amount of solute. This makes the physicochemical properties of the droplet (melting point, viscosity, carbon solubility) mainly determined by aluminum, making it more stable and controllable.
[0049] In other implementations, the thickness ratio of the silicon layer 20 to the aluminum layer 30 may also be less than 1:5.
[0050] During SiC growth using the VLS (Vacuum-Laser Light) growth mechanism, aluminum atoms in the solution replace silicon atoms in the silicon carbide lattice. Since aluminum is a trivalent element, replacing tetravalent silicon creates a hole, thus forming a p-type semiconductor. Aluminum is the dopant source; in this system, the pre-sputtered aluminum layer is the sole source of aluminum doping. The total mass of the aluminum layer (proportional to its thickness) directly determines the total amount of aluminum atoms available for doping.
[0051] The role of silicon layer 20 is to form eutectic droplets with aluminum, initiating the VLS process. As a reactant, it combines with dissolved carbon to form SiC.
[0052] In the Al-Si-C system, carbon atoms from the carbon source gas need to dissolve into Al-Si droplets. The dissolution and diffusion rate of carbon in the aluminum-based solution is one of the determining steps of the growth rate. The higher the reaction temperature, the higher the dissolution and diffusion rate of carbon, thus more effectively dissolving and transporting carbon atoms and promoting the continuous growth of SiC.
[0053] More specifically, the thickness of the p-type silicon carbide layer 40 is less than 1:10 in ratio to the length and width of each p-type silicon carbide layer 40. The thickness of the resulting uniform and smooth p-type silicon carbide layer 40 is only a few micrometers, and the length and width of the p-type silicon carbide layer 40 range from tens of micrometers to hundreds of micrometers. During the reaction process, the droplets formed by the silicon layer 20 and aluminum layer 30 during heating can still cover the target area under the action of surface tension.
[0054] In one embodiment, such as Figure 5 As shown, the specific process of placing the semiconductor substrate 10 with the silicon layer 20 and aluminum layer 30 formed in a vacuum high-temperature furnace in step S20 includes:
[0055] The semiconductor substrate 10, on which the silicon layer 20 and the aluminum layer 30 are formed, is placed in a high-temperature CVD furnace and evacuated to 10°C. -5 Pa, argon gas is introduced and heated to 1000-1800℃ until the aluminum layer 30 melts and the silicon in the silicon layer 20 dissolves in the molten aluminum, forming an aluminum-silicon mixed solution layer in a predetermined area on the surface of the semiconductor substrate 10; a mixture of carbon source gas and argon gas is introduced, and the carbon source gas decomposes upon contact with the surface of the hot aluminum-silicon mixed solution, and the carbon atoms in the carbon source gas dissolve into the aluminum-silicon mixed solution and diffuse, reacting with the silicon in the aluminum-silicon mixed solution to form silicon carbide on the surface of the predetermined area on the surface of the semiconductor substrate 10, and the aluminum in the aluminum-silicon mixed solution replaces the silicon in the silicon carbide, thereby forming a p-type silicon carbide layer 40.
[0056] More specifically, the flow ratio of carbon source gas to argon in the mixed gas is 4:50, and the carbon source gas includes at least one of methane, ethylene, propane, propylene, butane, and butene.
[0057] In other embodiments, the carbon source gas may be other gases, and the flow ratio of the carbon source gas to argon in the mixed gas may be other ranges.
[0058] For example, a semiconductor substrate 10 with a silicon layer 20 and an aluminum layer 30 formed by magnetron sputtering is placed in a high-temperature CVD furnace, and the vacuum control system is turned on until the vacuum level reaches 10. -5 After Pa, a certain amount of Ar is introduced to maintain the chamber pressure at 100-800 mbar, and the heating system is turned on to heat the chamber until the temperature reaches 1000-1800℃. During this process, because the temperature exceeds the melting point of Al (660℃), Al becomes liquid, and Si dissolves in the Al solution. At this point, a mixture of carbon source gas (C2H4, CH4, etc.) and Ar is introduced, with a flow ratio of carbon source gas to Ar of 4:50. The molecules of the carbon source gas break down upon contact with the hot aluminum-silicon mixed solution surface. Carbon atoms in the carbon source gas dissolve into the aluminum-silicon mixed solution and diffuse. The dissolved carbon atoms combine with silicon atoms that are also dissolved in the molten liquid, reaching supersaturation at the bottom of the droplet (i.e., the interface in contact with the substrate) and precipitating solid SiC crystals. As the SiC crystal grows, aluminum atoms replace the positions of silicon atoms in the silicon carbide lattice, forming a p-type silicon carbide layer 40.
[0059] In one embodiment, such as Figure 6As shown, in step S20, the cleaning process includes using a cleaning solution to remove residual reactants from the surface of the p-type silicon carbide layer 40. Furthermore, the cleaning solution is a strong acid cleaning solution.
[0060] The residual reactants 50 mainly consist of residual aluminum and silicon.
[0061] For example, the strong acid cleaning solution is a mixed solution of HF and HNO3. HF-HNO3 is a mixture of hydrofluoric acid and nitric acid. Nitric acid acts as a strong oxidant, and hydrofluoric acid acts as a complexing agent. The HF-HNO3 mixed solution combines the different chemical effects of the two acids to form a synergistic effect, which can dissolve the residual reactants 50 on the surface of the p-type silicon carbide layer 40.
[0062] This invention also provides a method for fabricating a silicon carbide device, comprising:
[0063] A p-type silicon carbide layer 40 is formed on the surface of a predetermined region of a semiconductor substrate 10 using the fabrication method of the p-type silicon carbide device structure described above.
[0064] A silicon carbide device is formed on the surface of the p-type silicon carbide layer 40.
[0065] The present invention provides a method for fabricating a p-type silicon carbide device structure that requires only three steps to obtain the p-type silicon carbide device structure, which greatly simplifies the fabrication process of the prior art and reduces production costs; and uses a mature VLS growth process, which fundamentally avoids the product quality problems caused by etching, photolithography and ion implantation processes.
[0066] Finally, it should be noted that any modification or equivalent substitution of some or all of the technical features based on the technical solutions disclosed in this invention and the technical solutions of the embodiments thereof, without departing from the corresponding technical solutions of this invention, shall fall within the patent scope of the device structure and the implementation scheme of this invention.
Claims
1. A method for fabricating a p-type silicon carbide device structure, characterized in that, include: A semiconductor substrate is provided, and a silicon layer and an aluminum layer are sequentially formed on a predetermined area on the surface of the semiconductor substrate using a mask; The semiconductor substrate with silicon and aluminum layers formed is placed in a vacuum high-temperature CVD furnace and heated until the aluminum layer melts and the silicon in the silicon layer dissolves in the molten aluminum, forming an aluminum-silicon mixed solution layer in a predetermined area on the surface of the semiconductor substrate. A carbon source gas is introduced, and the carbon source gas decomposes upon contact with the surface of the hot aluminum-silicon mixed solution. The carbon atoms in the carbon source gas dissolve into the aluminum-silicon mixed solution and diffuse, reacting with the silicon in the aluminum-silicon mixed solution to form silicon carbide on a predetermined area of the semiconductor substrate. The aluminum in the aluminum-silicon mixed solution replaces the silicon in the silicon carbide, thereby forming a p-type silicon carbide layer. The temperature of the semiconductor substrate is lowered to room temperature, and the residual reactants on the surface of the p-type silicon carbide layer are removed by a cleaning process, thereby forming a p-type silicon carbide layer on the surface of a predetermined region of the semiconductor substrate.
2. The method for fabricating a p-type silicon carbide device structure according to claim 1, characterized in that, The step of sequentially forming a silicon layer and an aluminum layer in a predetermined area on the surface of a semiconductor substrate using a mask includes: A metal mask is formed on the surface of the semiconductor substrate, the metal mask having an opening that exposes a predetermined area; a silicon layer and an aluminum layer are sequentially formed on the surface of the semiconductor substrate; the metal mask is removed, and stacked and discrete silicon and aluminum layers are formed in the predetermined area on the surface of the semiconductor substrate.
3. The method for fabricating a p-type silicon carbide device structure according to claim 2, characterized in that, The method for sequentially forming the silicon layer and the aluminum layer includes at least one of magnetron sputtering, electron beam evaporation, and thermal evaporation.
4. The method for fabricating a p-type silicon carbide device structure according to claim 1, characterized in that, The thickness ratio of the silicon layer to the aluminum layer is less than 1:
10.
5. The method for fabricating a p-type silicon carbide device structure according to claim 1, characterized in that, The ratio of the thickness of the p-type silicon carbide layer to the length-to-width ratio of each p-type silicon carbide layer is less than 1:
10.
6. The method for fabricating a p-type silicon carbide device structure according to claim 1, characterized in that, The specific process of placing the semiconductor substrate with silicon and aluminum layers in a vacuum high-temperature furnace includes: The semiconductor substrate with silicon and aluminum layers formed is placed in a high-temperature CVD furnace and evacuated to 10°C. -5 Pa, argon gas is introduced and heated to 1000-1800℃ until the aluminum layer melts. The silicon in the silicon layer dissolves in the molten aluminum, forming an aluminum-silicon mixed solution layer in a predetermined area on the surface of the semiconductor substrate. A mixture of carbon source gas and argon gas is introduced. The carbon source gas decomposes upon contact with the hot aluminum-silicon mixed solution surface. Carbon atoms in the carbon source gas dissolve into the aluminum-silicon mixed solution and diffuse, reacting with the silicon in the aluminum-silicon mixed solution to form silicon carbide on the surface of the predetermined area on the semiconductor substrate. The aluminum in the aluminum-silicon mixed solution replaces the silicon in the silicon carbide, thereby forming a p-type silicon carbide layer.
7. The method for fabricating a p-type silicon carbide device structure according to claim 6, characterized in that, The flow rate ratio of carbon source gas to argon in the mixed gas is 4:50, and the carbon source gas includes at least one of methane, ethylene, propane, propylene, butane, and butene.
8. The method for fabricating a p-type silicon carbide device structure according to claim 1, characterized in that, The cleaning process includes using a cleaning solution to remove residual reactants from the surface of the p-type silicon carbide layer; the cleaning solution is a strong acid cleaning solution.
9. The method for fabricating a p-type silicon carbide device structure according to claim 1, characterized in that, The semiconductor substrate is a silicon carbide wafer, a silicon wafer with a silicon carbide epitaxial layer on its surface, or a silicon wafer.
10. A method for fabricating a silicon carbide device, characterized in that, include: A p-type silicon carbide layer is formed on the surface of a predetermined region of the semiconductor substrate using the fabrication method of the p-type silicon carbide device structure as described in claim 1; A silicon carbide device is formed on the surface of the p-type silicon carbide layer.