CN106611776A - N-type silicon carbide Schottky diode structure - Google Patents
N-type silicon carbide Schottky diode structure Download PDFInfo
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- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 title claims abstract description 57
- 229910010271 silicon carbide Inorganic materials 0.000 title claims abstract description 57
- 230000002441 reversible effect Effects 0.000 claims abstract description 14
- 239000004020 conductor Substances 0.000 claims abstract description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 17
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 229910021420 polycrystalline silicon Inorganic materials 0.000 claims description 12
- 229920005591 polysilicon Polymers 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 9
- 235000012239 silicon dioxide Nutrition 0.000 claims description 8
- 238000000137 annealing Methods 0.000 claims description 6
- 238000005468 ion implantation Methods 0.000 claims description 4
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 3
- 238000000407 epitaxy Methods 0.000 claims description 3
- 239000003870 refractory metal Substances 0.000 claims description 3
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims 4
- 229910002451 CoOx Inorganic materials 0.000 claims 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 2
- 229910052593 corundum Inorganic materials 0.000 claims 2
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 claims 2
- GNRSAWUEBMWBQH-UHFFFAOYSA-N nickel(II) oxide Inorganic materials [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 claims 2
- 229910001845 yogo sapphire Inorganic materials 0.000 claims 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims 2
- 230000005684 electric field Effects 0.000 abstract description 11
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- 238000002513 implantation Methods 0.000 description 6
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- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 150000002500 ions Chemical class 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 239000010703 silicon Substances 0.000 description 5
- 238000005530 etching Methods 0.000 description 4
- 229920002120 photoresistant polymer Polymers 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
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- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
- H10D8/00—Diodes
- H10D8/60—Schottky-barrier diodes
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
- H10D62/00—Semiconductor bodies, or regions thereof, of devices having potential barriers
- H10D62/10—Shapes, relative sizes or dispositions of the regions of the semiconductor bodies; Shapes of the semiconductor bodies
- H10D62/102—Constructional design considerations for preventing surface leakage or controlling electric field concentration
- H10D62/103—Constructional design considerations for preventing surface leakage or controlling electric field concentration for increasing or controlling the breakdown voltage of reverse-biased devices
- H10D62/105—Constructional design considerations for preventing surface leakage or controlling electric field concentration for increasing or controlling the breakdown voltage of reverse-biased devices by having particular doping profiles, shapes or arrangements of PN junctions; by having supplementary regions, e.g. junction termination extension [JTE]
- H10D62/109—Reduced surface field [RESURF] PN junction structures
- H10D62/111—Multiple RESURF structures, e.g. double RESURF or 3D-RESURF structures
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
- H10D62/00—Semiconductor bodies, or regions thereof, of devices having potential barriers
- H10D62/80—Semiconductor bodies, or regions thereof, of devices having potential barriers characterised by the materials
- H10D62/83—Semiconductor bodies, or regions thereof, of devices having potential barriers characterised by the materials being Group IV materials, e.g. B-doped Si or undoped Ge
- H10D62/832—Semiconductor bodies, or regions thereof, of devices having potential barriers characterised by the materials being Group IV materials, e.g. B-doped Si or undoped Ge being Group IV materials comprising two or more elements, e.g. SiGe
- H10D62/8325—Silicon carbide
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Abstract
本发明涉及一种N型碳化硅肖特基二极管结构,包括以下特征:在N型碳化硅肖特基二极管器件体内没有P型掺杂区,其中至少有一个沟槽,这沟槽的深度为0.5um至6.0um之间,宽度为0.4um至4.0um之间,沟槽内壁(侧边和底部)有一介质层物质,厚度为0.01um至1um,沟槽中间填以导电物质。这种沟槽结构是用来扩展器件在反向偏置时的耗尽层,避免电场过度集中而引起器件局部提早击穿。
The invention relates to an N-type silicon carbide Schottky diode structure, which includes the following features: there is no P-type doped region in the body of the N-type silicon carbide Schottky diode device, and there is at least one groove, and the depth of the groove is Between 0.5um and 6.0um, the width is between 0.4um and 4.0um, there is a dielectric layer on the inner wall (side and bottom) of the groove, the thickness is 0.01um to 1um, and the middle of the groove is filled with conductive material. This trench structure is used to expand the depletion layer of the device when it is reverse biased, so as to avoid local premature breakdown of the device caused by excessive concentration of the electric field.
Description
技术领域technical field
本发明涉及一种N型碳化硅半导体器件的结构,更具体地说是涉及一种N型碳化硅肖特基二极管的新结构。The invention relates to a structure of an N-type silicon carbide semiconductor device, and more specifically relates to a new structure of an N-type silicon carbide Schottky diode.
背景技术Background technique
使用硅器件的传统集成电路大都只能工作在250℃以下,不能满足高温、高功率及高频等要求。当中,新型半导体材料碳化硅(SiC)最受人注目和研究。Most traditional integrated circuits using silicon devices can only work below 250°C, which cannot meet the requirements of high temperature, high power and high frequency. Among them, the new semiconductor material silicon carbide (SiC) has attracted the most attention and research.
碳化硅半导体材料具有宽带隙、高饱和漂移速度、高热导率、高临界击穿电场等突出优点,特别适合制作大功率、高压、高温、抗辐照电子器件。Silicon carbide semiconductor materials have outstanding advantages such as wide band gap, high saturation drift velocity, high thermal conductivity, and high critical breakdown electric field, and are especially suitable for the production of high-power, high-voltage, high-temperature, and radiation-resistant electronic devices.
碳化硅禁带宽度宽(210eV≤Eg≤710eV),漏电流比硅小几个数量级。而且,碳化硅热稳定性极好,本征温度可达800℃以上,它保证了在高温工作时的长期可靠性。通过分析优值,如Johnson优值(JFOM-通过材料的击穿电场、饱和电子漂移速度来反映相应器件的高功率、高频率性能)、Keyes优值(KFOM-通过材料的热导率、饱和电子漂移速度及介电常数反映相应器件的开关速度和热限制)及热优值(QFOM-通过材料的击穿电场、击穿电场及热导率反映相应器件的散热性能),会发现碳化硅SiC这几个优值都比现在常用的半导体材料高出很多,是实现结合高温与高频高功率的一种理想材料。Silicon carbide has a wide band gap ( 210eV≤E g≤710eV), and its leakage current is several orders of magnitude smaller than that of silicon. Moreover, silicon carbide has excellent thermal stability, and its intrinsic temperature can reach more than 800°C, which ensures long-term reliability when working at high temperature. By analyzing the figure of merit, such as the Johnson figure of merit (JFOM-reflecting the high power and high frequency performance of the corresponding device through the breakdown electric field and saturated electron drift velocity of the material), the Keyes figure of merit (KFOM-through the thermal conductivity of the material, saturation Electronic drift speed and dielectric constant reflect the switching speed and thermal limit of the corresponding device) and thermal figure of merit (QFOM-reflect the heat dissipation performance of the corresponding device through the breakdown electric field, breakdown electric field and thermal conductivity of the material), and silicon carbide will be found The merit values of SiC are much higher than the semiconductor materials commonly used today, and it is an ideal material for realizing the combination of high temperature and high frequency and high power.
碳化硅击穿电场较高,是硅材料的8倍,这对功率器件甚为关键。导通电阻是与击穿电场的立方成反比,所以碳化硅SiC功率器件的导通电阻只有硅器件的百至二百分之一,显着降低电子设备的能耗。因此,碳化硅SiC功率器件也被誉为带动“新能源革命”的“绿色能源”器件。用碳化硅SiC所制造出来的功率器件具有低比导通电阻,高工作频率和高温工作稳定性的优点,拥有很广阔的应用前景。Silicon carbide has a higher breakdown electric field, eight times that of silicon, which is critical for power devices. The on-resistance is inversely proportional to the cube of the breakdown electric field, so the on-resistance of silicon carbide SiC power devices is only one hundred to two hundredth of that of silicon devices, which significantly reduces the energy consumption of electronic equipment. Therefore, silicon carbide SiC power devices are also known as "green energy" devices that drive the "new energy revolution". Power devices made of silicon carbide SiC have the advantages of low specific on-resistance, high operating frequency and high temperature stability, and have broad application prospects.
随着6H、4H-SiC体材料的相继商品化,碳化硅SiC器件工艺,如氧化、掺杂、刻蚀及金属、半导体接触,都日渐成熟,这些为碳化硅SiC器件的研制及应用奠定了基础。With the successive commercialization of 6H and 4H-SiC bulk materials, silicon carbide SiC device processes, such as oxidation, doping, etching, and metal and semiconductor contacts, are becoming more and more mature, which lays the foundation for the development and application of silicon carbide SiC devices. Base.
600V和1200V N型碳化硅肖特基二极管是最早商品化的碳化硅器件,一般的碳化硅N型肖特基二极管的器件结构如图1所示,这结构的组成主要可以分为有源区与终端区,有源区由肖特基金属接触与PN结並连,终端区由场限环组成。因为碳化硅PN结的导通电压一般大于3V而肖特基金属接触的导通电压是1V左右,当正向导通电压少于3V时,导通电流主要是电子电流从衬底的阳极流经肖特基势垒进入表面阴极电极,所以是单一载流子器件。当器件处于反向偏置时,电子尝试从表面跨越肖特基势垒而进入碳化硅半导体内,在一般反偏置不是很大时,在表面电极內只有非常小的一部份电子能获得足够能量跨越势垒进入碳化硅半导体内而形成反向漏电流的一部份,当反偏较大时,有源区里的P型掺杂区的耗尽层会连接起来把表面的肖特基金属接触屏蔽起來,使得表面电极里的电子更难进入碳化硅半导体内,从而使得碳化硅肖特基二极管反向时,除了漏电流外是不导电的,所以肖特基二极管便成为单向导通器件。要形成图1的器件结构是要在碳化硅体內形成P型掺杂区的。基于碳化硅SiC的键强度高,杂质扩散所要求的温度(>1800℃),大大超过标准器件工艺的条件,所以器件制作工艺中的掺杂不能采用扩散工艺,只能利用外延控制掺杂和高温离子注入掺杂。600V and 1200V N-type silicon carbide Schottky diodes are the earliest commercialized silicon carbide devices. The device structure of a general silicon carbide N-type Schottky diode is shown in Figure 1. The composition of this structure can be mainly divided into active regions With the terminal area, the active area is connected in parallel with the Schottky metal contact and the PN junction, and the terminal area is composed of a field limiting ring. Because the conduction voltage of the SiC PN junction is generally greater than 3V and the conduction voltage of the Schottky metal contact is about 1V, when the forward conduction voltage is less than 3V, the conduction current is mainly the electron current flowing through the anode of the substrate The Schottky barrier goes into the surface cathode electrode, so it is a single carrier device. When the device is reverse biased, electrons try to cross the Schottky barrier from the surface and enter the silicon carbide semiconductor. When the general reverse bias is not very large, only a very small part of the electrons in the surface electrode can get Enough energy crosses the potential barrier into the silicon carbide semiconductor to form a part of the reverse leakage current. When the reverse bias is large, the depletion layer of the P-type doped region in the active region will be connected to the Schott of the surface. The base metal contact is shielded, making it more difficult for electrons in the surface electrode to enter the silicon carbide semiconductor, so that when the silicon carbide Schottky diode is reversed, it is non-conductive except for leakage current, so the Schottky diode becomes a unidirectional through devices. To form the device structure in FIG. 1 , it is necessary to form a P-type doped region in the silicon carbide body. Based on the high bond strength of SiC, the temperature required for impurity diffusion (>1800°C) greatly exceeds the conditions of the standard device process, so the doping process in the device manufacturing process cannot use the diffusion process, and can only be controlled by epitaxy. High temperature ion implantation doping.
外延掺杂可利用碳化硅源气体流量变化,使掺杂浓度控制在从轻掺杂(1014/cm3)到简并掺杂(>1019/cm3)的范围。硅烷、丙烷是碳化硅SiC典型的外延气体源。6H-SiC在硅(Si)面N型衬底上同质外延典型的生长速率为3μm/h。在生长反应室中,通过调节气体源的比例来进行位置竞争外延,使杂质位于晶格位置。在碳(C)面衬底上的生长则不同,但对其生长机制尚无深刻了解。Epitaxial doping can be controlled by changing the flow rate of silicon carbide source gas to control the doping concentration from light doping (10 14 /cm 3 ) to degenerate doping (>10 19 /cm 3 ). Silane and propane are typical epitaxial gas sources for silicon carbide SiC. The typical growth rate of 6H-SiC homoepitaxial growth on silicon (Si) surface N-type substrate is 3 μm/h. In the growth reaction chamber, site-competitive epitaxy is performed by adjusting the ratio of gas sources so that the impurities are located at the lattice sites. Growth on carbon (C) facet substrates is different, but its growth mechanism is not well understood.
因为不能采用扩散工艺掺杂,离子注入工艺在器件制作中非常重要。铝(Al)和硼(B)为典型的P型掺杂元素,产生相对深的受主能级(分别为211meV和300meV),Al的电离能小于B的电离能,Al要求的激活温度比B低;而B原子比Al原子轻,注入引起的损伤较少,且注入范围更深,应根据器件工艺要求来选择注入元素。Because the diffusion process cannot be used for doping, the ion implantation process is very important in device fabrication. Aluminum (Al) and boron (B) are typical P-type doping elements, which produce relatively deep acceptor energy levels (211meV and 300meV, respectively). The ionization energy of Al is smaller than that of B, and the activation temperature required by Al is higher than that of B is low; while B atoms are lighter than Al atoms, the damage caused by implantation is less, and the implantation range is deeper. The implantation elements should be selected according to the device process requirements.
可是,当离子注入碳化硅过大时,会引致晶格损伤,形成非晶化的结构,大大降低碳化硅原有的性能。为了减少注入离子时所引起的晶格损伤和非晶化结构出现,在注入离子时需对衬底加上高温,一般对N注入时需要约650℃,在对Al注入时需要约700~800℃。注入后,还需要经过高温退火热处理(>1300℃),把注入的离子激活,同时令注入离子时所引起的的晶格损伤复原。由于SiC的键强度高,需要在高温下才能产生晶格空缺,让掺杂离子填入,获得激活。文献报道了退火温度1300℃得到少于10%激活率;当温度大于1600℃时,激活率才会超过95%。However, when the ion implantation into silicon carbide is too large, it will cause damage to the crystal lattice and form an amorphous structure, greatly reducing the original performance of silicon carbide. In order to reduce the lattice damage and amorphization structure caused by implanting ions, it is necessary to add high temperature to the substrate when implanting ions. Generally, about 650 ° C is required for N implantation, and about 700-800 ° C is required for Al implantation. ℃. After the implantation, high-temperature annealing heat treatment (>1300°C) is required to activate the implanted ions and restore the crystal lattice damage caused by the implanted ions. Due to the high bond strength of SiC, lattice vacancies need to be generated at high temperatures to allow dopant ions to fill in and activate. It is reported in the literature that the annealing temperature is 1300°C and the activation rate is less than 10%; when the temperature is greater than 1600°C, the activation rate exceeds 95%.
当温度大于1300℃时,SiC内的Si会蒸发出来,器件晶圆表面亦会粗化,令器件效能降低。现有的工艺是在晶圆最顶层表面沉积碳化硅(SiC)或石墨(C)层作为保护,然后才进行退火热处理,退火后要把石墨层清除掉,形成P型掺杂区是关键的步骤,也是很增加成本的步骤,若果N型碳化硅肖特基二极管结构不需要P型掺杂区,制作成本上便可以大为降低。When the temperature is higher than 1300°C, the Si in SiC will evaporate, and the surface of the device wafer will also be roughened, reducing the performance of the device. The existing process is to deposit a silicon carbide (SiC) or graphite (C) layer on the top surface of the wafer as a protection, and then perform annealing heat treatment. After annealing, the graphite layer should be removed to form a P-type doped region. The steps are also very cost-increasing steps. If the N-type SiC Schottky diode structure does not require the P-type doped region, the manufacturing cost can be greatly reduced.
发明内容Contents of the invention
本发明的目的在于提出一种能避免上述不足而实用可行的一种有关N型碳化硅肖特基二基极管的有源区结构和终端区结构。使用本发明来制作N型肖特基二极管时可以不用注入P型掺杂区,也不用在N型外延层上长P型外延层,这可大大降低器件的制作成本。一般肖特基二极管的有源区或是终端区都是用P型掺杂区来扩展反向偏置时的耗尽层,避免耗尽层过于集中,即避免电场过度集中而引起器件局部提早击穿。本发明的核心思想是不用P型掺杂区来扩展器件在反向偏置时的耗尽层,而改用沟槽结构,这沟槽的深度为0.5um至6.0um之间,宽度为0.5um至4.0um之间,沟槽内壁(侧边和底部)有一层介质层物质如二氧化硅或氮化硅等,厚度为0.01um至1um,侧边的厚度与底部的厚度可以各自独立选取,有源区的沟槽与终端区沟槽可以各自独立选取其特征,中间填以导电物质如掺杂或非掺杂多晶硅或难容金属等。这种沟槽结构之所以能夠扩展外延层,因为当电场力線穿过沟槽介质后遇到沟槽中的导电物质时,电场力線无法穿越导电物质而绕道到旁边未耗尽的区域从而扩展了耗尽层,在图1中的有源区,沟槽结构在器件处于电压反偏置时能使耗尽层很快便扩展並连合起来而屏蔽掉肖特基金属接触,使反向电压只有一小部份落在肖特基势垒上,这会使得反向时的漏电流大为减少。在终端区处,如果没有任何终端结构处,如图2所示,在反向偏置时,电场会集中在有源区的边缘的表面处使器件提早击穿。假如在终端处恰当的位置放上以上所说的沟槽结构,这些沟槽单元会使反置时的耗尽层不至太集中而扩展开来,最终使器件达至最优化亦即最大的击穿电压。The object of the present invention is to propose a practical and feasible active region structure and terminal region structure related to N-type silicon carbide Schottky diodes which can avoid the above-mentioned disadvantages. When the invention is used to make the N-type Schottky diode, it is not necessary to inject the P-type doped region, nor to grow the P-type epitaxial layer on the N-type epitaxial layer, which can greatly reduce the manufacturing cost of the device. In general, the active region or terminal region of a Schottky diode uses a P-type doped region to expand the depletion layer during reverse bias, so as to avoid excessive concentration of the depletion layer, that is, to avoid excessive concentration of the electric field and cause local premature aging of the device. breakdown. The core idea of the present invention is not to expand the depletion layer of the device in reverse bias without the P-type doped region, but to use a trench structure. The depth of the trench is between 0.5um and 6.0um, and the width is 0.5um. Between um and 4.0um, there is a layer of dielectric material such as silicon dioxide or silicon nitride on the inner wall of the trench (side and bottom), with a thickness of 0.01um to 1um, and the thickness of the side and the bottom can be selected independently The characteristics of the trenches in the active region and the trenches in the terminal region can be independently selected, and the middle is filled with conductive substances such as doped or non-doped polysilicon or refractory metals. The reason why this trench structure can expand the epitaxial layer is that when the electric field force lines pass through the trench medium and meet the conductive material in the trench, the electric field force lines cannot pass through the conductive material and detour to the undepleted area next to it. The depletion layer is expanded. In the active region in Figure 1, the trench structure can quickly expand the depletion layer and join together when the device is under voltage reverse bias to shield the Schottky metal contact, so that the reverse Only a small part of the forward voltage falls on the Schottky barrier, which greatly reduces the leakage current in the reverse direction. At the termination region, if there is no termination structure, as shown in FIG. 2 , when reverse biased, the electric field will concentrate on the surface of the edge of the active region to cause early breakdown of the device. If the above-mentioned trench structure is placed at the appropriate position at the terminal, these trench units will make the depletion layer not too concentrated during inversion and will expand, and finally the device will be optimized, that is, the maximum breakdown voltage.
与现有技术相比,本发明的有益效果是能大为降低产品的研发周期,並使生产工序更简单易做,大大降低生产成本,並提高器件的性价比。Compared with the prior art, the invention has the beneficial effects of greatly reducing the product development cycle, making the production process simpler and easier to do, greatly reducing the production cost, and improving the cost performance of the device.
附图说明Description of drawings
附图用来提供对本发明的进一步理解,与本发明的实施例一起用于解释本发明,并不构成对本发明的限制:Accompanying drawing is used for providing further understanding to the present invention, is used for explaining the present invention together with the embodiment of the present invention, does not constitute limitation of the present invention:
图1是一般肖特基二极管结构示意图;Figure 1 is a schematic diagram of the structure of a general Schottky diode;
图2是没有任何终端结构的肖特基二极管结构示意图;FIG. 2 is a schematic diagram of a Schottky diode structure without any terminal structure;
图3是本发明实施例在表面上形成氧化层100和光刻涂层200的横切面示意图;FIG. 3 is a cross-sectional schematic diagram of forming an oxide layer 100 and a photoresist coating 200 on the surface according to an embodiment of the present invention;
图4是本发明实施例在表面暴露出沟槽开孔示意图;Fig. 4 is a schematic diagram of the opening of grooves exposed on the surface of the embodiment of the present invention;
图5是本发明实施例在沟槽内完成牺牲性氧化层示意图;Fig. 5 is a schematic diagram of completing a sacrificial oxide layer in a trench according to an embodiment of the present invention;
图6是本发明实施例在清除掉外延层表面上的氧化层和多晶硅层示意图;Fig. 6 is a schematic diagram of removing the oxide layer and the polysilicon layer on the surface of the epitaxial layer according to the embodiment of the present invention;
图7是本发明实施例形成接触孔示意图;7 is a schematic diagram of forming a contact hole according to an embodiment of the present invention;
图8是本发明实施例在碳化硅表面金属接触处留下一层鎳(肖特基金属接触)的示意图;Fig. 8 is a schematic diagram of leaving a layer of nickel (Schottky metal contact) at the silicon carbide surface metal contact according to the embodiment of the present invention;
图9是本发明实施例在碳化硅器件表面完成铝合金层的示意图。Fig. 9 is a schematic diagram of completing an aluminum alloy layer on the surface of a silicon carbide device according to an embodiment of the present invention.
参考符号表:Reference symbol table:
10 N型碳化硅衬底10 N-type silicon carbide substrate
20 碳化硅N型外延层20 SiC N-type epitaxial layer
30 二氧化硅层30 silicon dioxide layer
39 N型碳化硅体内的P型掺杂区39 P-type doped region in N-type silicon carbide body
40 P型高掺杂的多晶硅40 P-type highly doped polysilicon
50 层间介质50 interlayer medium
60 Ni金属层(肖特基金属接触)60 Ni metal layer (Schottky metal contact)
70 铝合金层70 aluminum layers
100 二氧化硅层100 silica layers
200 光刻涂层200 photolithographic coating
具体实施方式detailed description
以下结合附图对本发明的优选实施例进行说明,应当理解,此处所描述的优选实施例仅用于说明和解释本发明,并不用于限定本发明。The preferred embodiments of the present invention will be described below in conjunction with the accompanying drawings. It should be understood that the preferred embodiments described here are only used to illustrate and explain the present invention, and are not intended to limit the present invention.
实施例:Example:
如图3所示,首先将N型碳化硅外延层20置于N型碳化硅衬底10的上方,接着在外延层的上面采用积淀方式形成二氧化硅(SiO2)层100(厚度为0.01um至2um氧化物硬光罩),在氧化层上再积淀一层光刻涂层200。As shown in FIG. 3 , the N-type silicon carbide epitaxial layer 20 is first placed on the top of the N-type silicon carbide substrate 10, and then a silicon dioxide (SiO2) layer 100 (thickness of 0.01 μm) is formed by deposition on the epitaxial layer. to 2um oxide hard mask), and then deposit a layer of photoresist coating 200 on the oxide layer.
如图4所示,然后通过沟槽掩模形成图案暴露出氧化层的一些部分,接着对沟槽掩模形成图案暴露出的氧化层进行干蚀后,暴露出外延层。As shown in FIG. 4 , some parts of the oxide layer are exposed by patterning the trench mask, and then the epitaxial layer is exposed after dry etching the oxide layer exposed by patterning the trench mask.
如图5所示,然后清除掉光刻涂层,接着通过蚀刻形成沟槽(深度为0.5um至6.0um,宽度为0.1um至4.0um),然后对沟槽进行牺牲性氧化(时间为10分钟至100分钟,温度为1000℃至1200℃),以消除在开槽过程中被等离子破坏的碳化硅层。As shown in Figure 5, the photolithographic coating is then removed, followed by etching to form a trench (0.5um to 6.0um in depth, 0.1um to 4.0um in width), and then sacrificial oxidation of the trench (time 10 minutes to 100 minutes at a temperature of 1000°C to 1200°C) to eliminate the silicon carbide layer damaged by the plasma during the slotting process.
如图6所示,然后清除掉外延层表面和沟槽内所有氧化层,接着通过沉积方式,在沟槽暴露着的侧壁和底部,和外延层的上表面形成一层二氧化硅层30(厚度为0.01um至1um),接着在沟槽中和外延层的上表面沉积P型高掺杂剂的多晶硅40,多晶硅掺杂浓度为RS=15Ω/□至100Ω/□(方阻),以填充沟槽并覆盖顶面,然后对在外延层表面上的氧化层和多晶硅层进行平面腐蚀处理或化学机械,最终清除掉外延层表面上的氧化层。As shown in FIG. 6, all oxide layers on the surface of the epitaxial layer and in the trench are then removed, and then a silicon dioxide layer 30 is formed on the exposed sidewall and bottom of the trench and on the upper surface of the epitaxial layer by deposition. (thickness is 0.01um to 1um), then deposit P-type high-dopant polysilicon 40 in the trench and on the upper surface of the epitaxial layer, the polysilicon doping concentration is R S =15Ω/□ to 100Ω/□ (square resistance) , to fill the trench and cover the top surface, and then perform planar etching or chemical mechanical treatment on the oxide layer and polysilicon layer on the surface of the epitaxial layer, and finally remove the oxide layer on the surface of the epitaxial layer.
如图7所示,将碳化硅表面清洗干净,之后在外延层最表面上先沉积无掺杂二氧化硅层(厚度为0.1um至0.5um),然后沉积硼磷玻璃(厚度为0.1um至0.8um),形成层间介质50,接着在层间介质表面积淀光刻涂层,利用接触孔掩模暴露出部分层间介质,然后对暴露出的部分层间介质进行干蚀,直至暴露出碳化硅外延层的上表面,在层间介质中形成接触孔掩模开孔。As shown in Figure 7, the silicon carbide surface is cleaned, and then an undoped silicon dioxide layer (with a thickness of 0.1um to 0.5um) is deposited on the outermost surface of the epitaxial layer, and then borophosphoglass (with a thickness of 0.1um to 0.5um) is deposited. 0.8um) to form an interlayer dielectric 50, then deposit a photolithographic coating on the surface of the interlayer dielectric, use a contact hole mask to expose part of the interlayer dielectric, and then perform dry etching on the exposed part of the interlayer dielectric until it is exposed On the upper surface of the silicon carbide epitaxial layer, a contact hole mask opening is formed in the interlayer dielectric.
如图8所示,在接触孔底部以及层间介质上表面沉积一层鎳(Ni)层60,接着清除掉光刻涂层,藉着Life-off方法,在剝离光刻涂层时把不需要的Ni金属层去掉。As shown in FIG. 8, a layer of nickel (Ni) layer 60 is deposited on the bottom of the contact hole and the upper surface of the interlayer dielectric, and then the photoresist coating is removed. By the Life-off method, when the photoresist coating is stripped, the The unnecessary Ni metal layer is removed.
如图9所示,对Ni金属层进行适当的退火工艺來使Ni金属在碳化硅表面形成肖特基金属接触,接着在该器件的上面沉积一层铝合金70(厚度为0.8um至10um),然后通过金属掩模进行金属浸蚀,形成发射区金属垫层和和终端区场板。As shown in Figure 9, an appropriate annealing process is performed on the Ni metal layer to make the Ni metal form a Schottky metal contact on the surface of the silicon carbide, and then a layer of aluminum alloy 70 (thickness 0.8um to 10um) is deposited on the device. , and then conduct metal etching through the metal mask to form a metal pad layer in the emitter region and a field plate in the terminal region.
最后应说明的是:以上仅为本发明的实施例而已,并不用于限制本发明,本发明的有源区结构可用于涉及制造N型碳化硅肖特基二极管,本发明亦可用于P型器件,本发明的终端区结构可用于涉及制造N型碳化硅器件包括肖特基二极管,或绝缘栅晶体管(MOS),或绝缘栅双极晶体管(IGBT)或PiN二极管。尽管参照实施例对本发明进行了详细的说明,对于本领域的技术人员来说,其依然可以对前述各实施例所记载的技术方案进行修改,或者对其中部分技术特征进行等同替换,但是凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之。Finally, it should be noted that the above is only an embodiment of the present invention, and is not intended to limit the present invention. The active region structure of the present invention can be used to manufacture N-type silicon carbide Schottky diodes, and the present invention can also be used for P-type For devices, the termination region structure of the present invention can be used to manufacture N-type silicon carbide devices including Schottky diodes, or insulated gate transistors (MOS), or insulated gate bipolar transistors (IGBTs) or PiN diodes. Although the present invention has been described in detail with reference to the embodiments, those skilled in the art can still modify the technical solutions described in the foregoing embodiments, or perform equivalent replacements for some of the technical features. Within the spirit and principles of the present invention, any modifications, equivalent replacements, improvements, etc., shall be included in the protection scope of the present invention.
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Application publication date: 20170503 |