CN106098797A - 一种二极管用外延片及其制备方法 - Google Patents
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- 238000002360 preparation method Methods 0.000 title claims abstract description 13
- 239000000758 substrate Substances 0.000 claims abstract description 31
- 229910004205 SiNX Inorganic materials 0.000 claims abstract description 22
- 239000011435 rock Substances 0.000 claims abstract description 17
- 229910052594 sapphire Inorganic materials 0.000 claims abstract description 13
- 239000010980 sapphire Substances 0.000 claims abstract description 13
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- 238000011065 in-situ storage Methods 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 7
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 claims abstract description 6
- 238000001755 magnetron sputter deposition Methods 0.000 claims abstract description 5
- 238000005240 physical vapour deposition Methods 0.000 claims description 4
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 claims description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 3
- 238000000151 deposition Methods 0.000 claims description 2
- 239000010410 layer Substances 0.000 claims 29
- 239000002344 surface layer Substances 0.000 claims 1
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- 230000005611 electricity Effects 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 238000005516 engineering process Methods 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000013517 stratification Methods 0.000 description 2
- 238000003763 carbonization Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
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Abstract
本发明公开了一种肖特基二极管用外延片及其制备方法,其制成的二极管的晶体质量好,使用寿命长,反向击穿电压高、漏电低。该外延片的制作方法,依次包括如下步骤:A、将AlN盖层通过磁控溅射技术在蓝宝石平片上沉积制得衬底;B、将衬底放入MOCVD设备中加热升温至1040~1100℃,在30~400mbar的压力条件下,在衬底上直接生长GaN二维生长层;C、在950~1050℃温度下,在GaN二维生长层上原位生长SiNx模板层;D、在1000~1080℃温度下,在SiNx模板层上依次生长GaN恢复层和重掺杂nGaN层;E、保持温度不变,在重掺杂nGaN层上生长轻掺杂nGaN层;F、降温至600~750℃,在轻掺杂nGaN层上生长C掺杂的CBGaN帽层。
Description
技术领域
本发明涉及半导体制造技术领域,具体涉及一种二极管用外延片及其制备方法。
背景技术
肖特基二极管利用金属与半导体接触形成的金属-半导体接触原理制作而成,是一种热载流子二极管,具有低正向电压、超高速等特点,被广泛地应用在高频、大电流、低电压整流电路以及微波电子混频电路、检波电路、高频数字逻辑电路、交流-直流变换系统中,是电子器件中常见的分立器件。现有技术中,肖特基二极管普遍采用外延片作为其半导体部件。而用于GaN肖特基二极管的外延片的衬底主要有三种,即蓝宝石衬底、硅衬底和碳化硅衬底。其中,由于碳化硅的价格昂贵,而Si衬底不适合用于制作垂直结构的肖特基二极管,故蓝宝石衬底在垂直结构的肖特基二极管中应用更为广泛。现有技术中普遍使用的平片状蓝宝石衬底由于其位错密度较高,制成的二极管电子器件漏电流较高、易击穿、晶体质量不高。
发明内容
本发明的目的是提供一种二极管外延片及其制备方法,制成的外延片的电流密度小、反向击穿电压高,位错密度低,有效减少了由其制成的二极管终端器件的漏电通道,显著提高了器件的反向击穿电压和正向导通电流,增加了器件的使用寿命。
为达到上述目的,本发明采用的一种技术方案是:一种二极管用外延片的制备方法,依次包括如下步骤:
A、将AlN盖层通过磁控溅射技术在蓝宝石平片上沉积制得衬底;
B、将所述衬底放入MOCVD设备中加热升温至1040~1100℃,在30~400mbar的压力条件下,在所述衬底上直接生长GaN二维生长层;
C、在950~1050℃温度下,在所述GaN二维生长层上原位生长SiNx模板层;
D、在1000~1080℃温度下,在所述SiNx模板层上依次生长GaN恢复层和重掺杂nGaN层;
E、保持温度不变,在所述重掺杂nGaN层上生长轻掺杂nGaN层;
F、降温至600~750℃,在所述轻掺杂nGaN层上生长C掺杂的CBGaN帽层。
优选地,步骤C中,在所述GaN二维生长层上使用SiH4和NH3原位生长形成了所述SiNx模板层。
优选地,步骤A中,所述AlN盖层是通过PVD或sputter设备在蓝宝石平片上沉积制成所述衬底,所述AlN盖层的厚度为5~200nm。
优选地,所述重掺杂nGaN层、轻掺杂nGaN层的生长压力均为200~700mbar。
优选地,所述CBGaN帽层的生长压力为100~400mbar。
本发明的又一技术方案为:
一种如上述制备方法制备的二极管用外延片,包括:具有AlN盖层的衬底;通过MOCVD技术沉积于所述衬底上表面的GaN二维生长层;原位生长在所述GaN二维生长层上表面上的SiNx模板层;依次生长在所述SiNx模板层上表面上的GaN恢复层、重掺杂nGaN层、轻掺杂nGaN、CBGaN帽层。
优选地,所述SiNx层的厚度低于一个原子层的厚度。
优选地,所述GaN缓冲层的厚度为0.3~1μm;所述GaN恢复层的厚度为2~5μm;所述重掺杂nGaN层的厚度为2~3.5μm;所述轻掺杂nGaN层的厚度为4~12μm,所述CBGaN帽层的厚度为1~20nm。
优选地,所述重掺杂nGaN层和轻掺杂nGaN层的掺杂源为SiH4,其掺杂浓度分别为1E18~1.5E19cm-3和3E15~1.5E16cm-3。
优选地,所述CBGaN帽层中C的掺杂源为CBr4,其掺杂浓度为5E18~1E20cm-3。
本发明采用以上技术方案,相比现有技术具有如下优点:
1、本发明的衬底通过在蓝宝石平片上覆盖AlN盖层来替代低温GaN缓冲层,同时在GaN二维生长层上原位生长SiNx模板层,显著减少了刃位错密度和螺位错密度,使二极管外延片结构的XRD102和002分别降低至100arcsec和80arcsec以下,总位错密度降低至5*107/cm3以下。低位错密度减少了肖特基二极管终端器件的漏电通道,可显著提高反向击穿电压和正向导通电流,提高了外延片的晶体质量、增加了器件的使用寿命;同时还节约了生长时间。
2、本发明中还采用了CBGaN帽层结构,该CBGaN帽层的生长使用了CBr4作为C的掺杂源,帽层中有较高的碳含量,使得帽层中电阻率显著提升。该帽层起到了使电流横向扩展,减小电流密度的作用。因此可有效提高器件的反向击穿电压。
附图说明
为了更清楚地说明本发明实施例中的技术方案,下面将对实施例描述中所需要使用的附图作简单地介绍,显而易见地,下面描述中的附图仅仅是本发明的一些实施例,对于本领域普通技术人员来讲,在不付出创造性劳动的前提下,还可以根据这些附图获得其它的附图,其中:
附图1是本发明所述的二极管用外延片的结构示意图。
上述附图中:1、衬底;11、蓝宝石平片;12、AlN盖层;2、GaN二维生长层;3、SiNx模板层;4、GaN恢复层;5、重掺杂nGaN层;6、轻掺杂nGaN层;7、CBGaN帽层。
具体实施方式
下面结合附图来对本发明的技术方案作进一步的阐述。
参见图1所示,一种二极管用外延片,包括依次层叠设置的衬底、GaN二维生长层、SiNx模板层、GaN恢复层、重掺杂nGaN层、轻掺杂nGaN层、CBGaN帽层。
其中,该衬底为带有AlN盖层12的蓝宝石平片11衬底,该衬底由AlN盖层12采用PVD或sputter设备在蓝宝石平片11上磁控溅射沉积而成,该AlN盖层12厚度为5~200nm。
该SiNx模板层是在GaN二维生长层上使用SiH4和NH3原位生长形成的,该SiNx层的厚度低于一个原子层的厚度。
这里,通过采用AlN盖层12替代了低温GaN层,同时配合SiNx模板层,可显著减少了整个外延片的刃位错密度和螺位错密度,使肖特基二极管外延片结构的XRD102和002分别降低至100arcsec和80arcsec以下,总位错密度降低至5*107/cm3以下。低位错密度减少了肖特基二极管终端器件的漏电通道,可显著提高反向击穿电压和正向导通电流,提高了外延片的晶体质量,增加了器件的使用寿命,同时还节约了外延片的生长时间。
而这里采用了CBGaN帽层结构,该CBGaN帽层的生长使用了CBr4作为C的掺杂源,掺杂浓度为5E18~1E20cm-3。帽层中有较高的碳含量,使得帽层中电阻率显著提升。该帽层起到了使电流横向扩展,减小电流密度的作用。因此可有效提高器件的反向击穿电压。
一种上述二极管用外延片的制备方法,依次包括如下步骤:
A、将AlN盖层12利用PVD或sputter设备采用磁控溅射技术在蓝宝石平片11上沉积制得衬底,AlN盖层12的厚度为5~200nm;
B、将衬底放入MOCVD设备中加热升温至1040~1100℃,在30~400mbar的压力条件下,在衬底上直接生长GaN二维生长层;
C、在950~1050℃温度下,在GaN二维生长层上原位生长SiNx模板层;
D、在1000~1080℃温度下,在SiNx模板层上依次生长GaN恢复层和重掺杂nGaN层;
E、保持温度不变,在重掺杂nGaN层上生长轻掺杂nGaN层;
F、降温至600~750℃,在轻掺杂nGaN层上生长C掺杂的CBGaN帽层。
优选地,所述重掺杂nGaN层、轻掺杂nGaN层的生长压力均为200~700mbar。
优选地,所述CBGaN帽层的生长压力为100~400mbar。
这里,该GaN二维生长层的厚度为0.3~1μm;GaN恢复层的厚度为2~5μm;重掺杂nGaN层的厚度为2~3.5μm;轻掺杂nGaN层的厚度为4~12μm,CBGaN帽层的厚度为1~20nm。
重掺杂nGaN层和轻掺杂nGaN层的掺杂源均为SiH4,其掺杂浓度分别为1E18~1.5E19cm-3和3E15~1.5E16cm-3。
其中,GaN二维生长层的生长压力为30~400mbar;重掺杂nGaN层、轻掺杂nGaN层的生长压力均为200~700mbar;而CBGaN帽层的生长压力为100~400mbar。
上述实施例只为说明本发明的技术构思及特点,其目的在于让熟悉此项技术的人士能够了解本发明的内容并加以实施,并不能以此限制本发明的保护范围,凡根据本发明精神实质所作的等效变化或修饰,都应涵盖在本发明的保护范围内。
Claims (10)
1.一种二极管用外延片的制备方法,其特征在于,依次包括如下步骤:
A、将AlN盖层通过磁控溅射技术在蓝宝石平片上沉积制得衬底;
B、将所述衬底放入MOCVD设备中加热升温至1040~1100℃,在30~400mbar的压力条件下,在所述衬底上直接生长GaN二维生长层;
C、在950~1050℃温度下,在所述GaN二维生长层上原位生长SiNx模板层;
D、在1000~1080℃温度下,在所述SiNx模板层上依次生长GaN恢复层和重掺杂nGaN层;
E、保持温度不变,在所述重掺杂nGaN层上生长轻掺杂nGaN层;
F、降温至600~750℃,在所述轻掺杂nGaN层上生长C掺杂的CBGaN帽层。
2.根据权利要求1所述的制备方法,其特征在于,步骤C中,在所述GaN二维生长层上使用SiH4和NH3原位生长形成了所述SiNx模板层。
3.根据权利要求1所述的制备方法,其特征在于,步骤A中,所述AlN盖层是通过PVD或sputter设备在蓝宝石平片上沉积制成所述衬底,所述AlN盖层的厚度为5~200nm。
4.根据权利要求1所述的制备方法,其特征在于,所述重掺杂nGaN层、轻掺杂nGaN层的生长压力均为200~700mbar。
5.根据权利要求1所述的制备方法,其特征在于,所述CBGaN帽层的生长压力为100~400mbar。
6.一种如权利要求1~5任一项权利要求所述的制备方法制备的二极管用外延片,其特征在于,包括:具有AlN盖层的衬底;通过MOCVD技术沉积于所述衬底上表面的GaN二维生长层;原位生长在所述GaN二维生长层上表面上的SiNx模板层;依次生长在所述SiNx模板层上表面上的GaN恢复层、重掺杂nGaN层、轻掺杂nGaN、CBGaN帽层。
7.根据权利要求6所述的二极管用外延片,其特征在于,所述SiNx层的厚度低于一个原子层的厚度。
8.根据权利要求6所述的二极管用外延片,其特征在于,所述GaN缓冲层的厚度为0.3~1μm;所述GaN恢复层的厚度为2~5μm;所述重掺杂nGaN层的厚度为2~3.5μm;所述轻掺杂nGaN层的厚度为4~12μm,所述CBGaN帽层的厚度为1~20nm。
9.根据权利要求6所述的二极管用外延片,其特征在于,所述重掺杂nGaN层和轻掺杂nGaN层的掺杂源为SiH4,其掺杂浓度分别为1E18~1.5E19cm-3和3E15~1.5E16 cm-3。
10.根据权利要求6所述的二极管用外延片,其特征在于,所述CBGaN帽层中C的掺杂源为CBr4,其掺杂浓度为5E18~1E20 cm-3。
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