CN106299025A - 一种管式pecvd沉积氮化硅的工艺 - Google Patents
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- 238000000034 method Methods 0.000 title claims abstract description 25
- 229910052581 Si3N4 Inorganic materials 0.000 title claims abstract description 11
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 title claims abstract 4
- MEYZYGMYMLNUHJ-UHFFFAOYSA-N tunicamycin Natural products CC(C)CCCCCCCCCC=CC(=O)NC1C(O)C(O)C(CC(O)C2OC(C(O)C2O)N3C=CC(=O)NC3=O)OC1OC4OC(CO)C(O)C(O)C4NC(=O)C MEYZYGMYMLNUHJ-UHFFFAOYSA-N 0.000 claims abstract description 40
- 238000007747 plating Methods 0.000 claims abstract description 26
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 17
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 9
- 229910021529 ammonia Inorganic materials 0.000 claims description 8
- 229910000077 silane Inorganic materials 0.000 claims description 8
- 239000010408 film Substances 0.000 abstract description 28
- 230000000694 effects Effects 0.000 abstract description 15
- 239000010409 thin film Substances 0.000 abstract description 13
- 238000000151 deposition Methods 0.000 abstract description 12
- 229910052710 silicon Inorganic materials 0.000 abstract description 9
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- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 8
- 230000008569 process Effects 0.000 abstract description 3
- 239000013078 crystal Substances 0.000 abstract description 2
- 150000004767 nitrides Chemical class 0.000 abstract description 2
- 238000002161 passivation Methods 0.000 description 11
- 238000000576 coating method Methods 0.000 description 9
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- 239000007789 gas Substances 0.000 description 7
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- UMVBXBACMIOFDO-UHFFFAOYSA-N [N].[Si] Chemical compound [N].[Si] UMVBXBACMIOFDO-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 229910004205 SiNX Inorganic materials 0.000 description 2
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Abstract
一种管式PECVD沉积氮化硅的工艺,使用两步镀膜,镀第一层膜时使用的温度低于镀第二层膜时使用的温度。本发明提供的沉积工艺提高管式PECVD沉积氮化硅薄膜对晶硅太阳电池的钝化减反射效果以及降低工艺时间。
Description
技术领域
本发明属于光伏技术领域,尤其涉及一种管式PECVD沉积氮化硅的工艺。
背景技术
SiNx薄膜具有钝化硅片表面和减反射的作用,在晶体硅太阳电池的传统制备工艺中,使用等离子增强化学气相沉积(PECVD)的方法在发射极表面沉积一层SiNx薄膜是其中非常重要一步。
PECVD是借助微波或射频等使含有薄膜组成原子的气体电离,在局部形成等离子体,而等离子体化学活性很强,很容易发生反应,在基片上沉积出所期望的薄膜。为了使化学反应能在较低的温度下进行,利用了等离子体的活性来促进反应,因而这种CVD称为等离子体增强化学气相沉积(PECVD)。在目前实际生产中常用的管式低频直接法PECVD采用电阻式加热将整个腔体加热到所需的温度,在腔体中放置具有很多夹板的石墨舟,夹板的两侧放置硅片,利用两片硅片之间形成电势差与反应气体完成辉光放电进行镀膜,这种方法具有钝化效果好,同时成膜致密性高等优点。
然而,使用这种方法制备SiNx膜,当温度较低时,薄膜中存在大量的未分解完全的亚稳态的SiHx,这种分子会影响到表面的钝化特性;而在400℃沉积时这部分Si-H被充分分解,钝化水平提高。而当温度升高至450℃以上时,会有较多的氢分子从薄膜中释放出来,导致氢钝化效果变差。镀膜温度较低时则会导致镀膜时间较长,同时对二十一片石墨舟进行镀膜过程中石墨舟易受热不均匀导致出现色差片。
本专利是针对管式PECVD沉积氮化硅提出的兼顾镀膜时间以及镀膜良品率的一种有效提高电池效率的新型镀膜工艺。
发明内容
鉴于现有技术中存在的问题,本发明的目的在于提供一种管式PECVD沉积氮化硅的工艺。本发明提供的沉积工艺提高管式PECVD沉积氮化硅薄膜对晶硅太阳电池的钝化减反射效果以及降低工艺时间。
为达此目的,本发明采用以下技术方案:
一种管式PECVD沉积氮化硅的工艺,使用两步镀膜,两层膜采用不同的镀膜工艺条件,尤其是沉积温度上,镀第一层膜时使用的温度低于镀第二层膜时使用的温度,可在保证生产效率的同时有效提高电池光电转换效率。
作为优选,镀第一层膜时的温度为400~450℃,例如为405℃、412℃、419℃、425℃、431℃、438℃、444℃、448℃等,时间为150~200s,例如为155s、164s、171s、178s、185s、192s、199s等;镀第二层膜时的温度为460~500℃,例如为465℃、472℃、479℃、485℃、491℃、498℃等,时间为300~400s,例如为305s、314s、321s、328s、335s、342s、349s、355s、364s、371s、380s、386s、397s等。第一层膜作用起钝化效果,镀第一层膜的最佳温度是400~450℃,温度过高会导致钝化效果变差。而第二层主要承担提高光吸收的作用,镀第二层膜的最佳温度是460~500℃,适当提高温度可以提高沉积速率同时使膜结构更加疏松利于降低薄膜对光的自吸收。
氮化硅薄膜的折射率为:
需要取得最低反射率,当在折射率为n0和n2的两层介质膜之间***折射率为n1的介质膜时,折射率之间满足其中,n0是硅的折射率,n2是第二层膜折射率;或者n0为第一层膜折射率,n2为玻璃(玻璃是指封装电池的组件端玻璃)的折射率。同时SiNx薄膜存在自吸收现象,折射率越高,自吸收现象越明显,故第一层膜的厚度不宜过厚,可通过反应气体比例调整适当的折射率。
作为优选,镀第一层膜时使用的氨气与硅烷的气体流量比低于镀第二层膜时使用的氨气与硅烷的气体流量比。
优选地,镀第一层膜时的氨气与硅烷的气体流量比(NH3/SiH4)为3.5~4.5,例如为3.7、3.9、4.1、4.4等,镀第一层膜时的氨气与硅烷的气体流量比为8.5~9.5,例如为8.7、8.9、9.1、9.4等。
本发明所使用的镀膜工艺使用两步镀膜工艺,第一层膜和第二层膜采用不同的工艺条件进行沉积。第一层膜主要起钝化效果,可以使用较高的硅烷和氨气气体流量比,以获得较高的氮化硅薄膜硅氮比例,同时使用较低的镀膜沉积温度。第二层膜选用较低的硅氮比,同时提高镀膜沉积温度。
作为优选,镀膜时的压力为1650~1705torr,例如为1655torr、1674torr、1680torr、1689torr、1695torr、1700torr等。镀第一层膜和第二层膜的压力可相同或不同。
作为优选,镀第一层膜时的射频功率为6000~6300W,例如为6010W、6040W、6080W、6120W、6180W、6240W、6290W等,镀第二层膜时的射频功率为7000~7300W,例如为7010W、7040W、7080W、7120W、7180W、7240W、7290W等。
作为优选,镀第一层膜时的脉冲开关比为1/9~1/11,镀第二层膜时的脉冲开关比为1/7~1/9。
相较于传统的双层膜技术,本发明的工艺除在两层膜的折射率上存在不同,同时第一层膜温度较低,使用较低的RF功率和较低的脉冲开关比,使得第一次膜沉积速度慢,成膜质量好,同时温度低,氢钝化效果好。而第二层膜使用高温沉积,有效整体降低镀膜工艺总时间,同时RF功率和脉冲比较高导致成膜致密度较差,降低了薄膜的自吸收现象,可以有效提高光电流。
本发明通过在使用双层膜镀膜工艺,两层膜采用合适的硅氮比,同时第一层膜使用降低温度沉积条件保证薄膜钝化效果,第二层使用高温沉积的条件下,降低工艺时间,同时使第二层膜成膜疏松,有效降低了薄膜的自吸收现象。
附图说明
图1是双层膜的结构示意图。
下面对本发明进一步详细说明。但下述的实例仅仅是本发明的简易例子,并不代表或限制本发明的权利保护范围,本发明的保护范围以权利要求书为准。
具体实施方式
下面结合附图并通过具体实施方式来进一步说明本发明的技术方案。
为更好地说明本发明,便于理解本发明的技术方案,本发明的典型但非限制性的实施例如下:
实施例1
使用如下表1中工艺参数进行镀膜实验。
表1
实施例2
使用如下表2中工艺参数进行镀膜实验。
表2
实施例3
使用如下表3中工艺参数进行镀膜实验。
表3
图1是双层膜的结构示意图。
对比例1
使用如下表4中的常规双层膜工艺进行镀膜。
表4
结果测试
分别使用这两种工艺进行镀膜实验后,得到的总膜厚基本一致,最终镀膜工艺时间降低了40s,同时这两种工艺所得膜的电学性能的对比如下表5中所示。
表5
Eta(%) | Isc(A) | Uoc(V) | FF(%) | Rs(mΩ) | Rsh(Ω) | |
实施例1 | 18.29 | 8.87 | 0.634 | 79.14 | 1.51 | 675.01 |
实施例2 | 18.27 | 8.89 | 0.635 | 78.63 | 1.57 | 600.95 |
实施例3 | 18.26 | 8.88 | 0.633 | 79.06 | 1.46 | 731.08 |
对比例1 | 18.24 | 8.86 | 0.634 | 78.96 | 1.53 | 567.49 |
由电学性能可见,本发明所使用工艺有效提高了电池光电转化效率,主要体现在短路电流有所增大,并联电阻则明显提升,这得益于氮化硅薄膜氢钝化效果的提升。
本发明并不仅限于实施例,其他本领域人员根据本发明所做的相关非本质改变,同样应是本发明所保护的范围。
申请人声明,本发明通过上述实施例来说明本发明的详细结构特征,但本发明并不局限于上述详细结构特征,即不意味着本发明必须依赖上述详细结构特征才能实施。所属技术领域的技术人员应该明了,对本发明的任何改进,对本发明所选用部件的等效替换以及辅助部件的增加、具体方式的选择等,均落在本发明的保护范围和公开范围之内。
以上详细描述了本发明的优选实施方式,但是,本发明并不限于上述实施方式中的具体细节,在本发明的技术构思范围内,可以对本发明的技术方案进行多种简单变型,这些简单变型均属于本发明的保护范围。
另外需要说明的是,在上述具体实施方式中所描述的各个具体技术特征,在不矛盾的情况下,可以通过任何合适的方式进行组合,为了避免不必要的重复,本发明对各种可能的组合方式不再另行说明。
此外,本发明的各种不同的实施方式之间也可以进行任意组合,只要其不违背本发明的思想,其同样应当视为本发明所公开的内容。
Claims (7)
1.一种管式PECVD沉积氮化硅的工艺,使用两步镀膜,其特征在于,镀第一层膜时使用的温度低于镀第二层膜时使用的温度。
2.根据权利要求1所述的工艺,其特征在于,镀第一层膜时的温度为400~450℃,时间为150~200s;镀第二层膜时的温度为460~500℃,时间为300~400s。
3.根据权利要求1或2所述的工艺,其特征在于,镀第一层膜时使用的氨气与硅烷的气体流量比低于镀第二层膜时使用的氨气与硅烷的气体流量比。
4.根据权利要求1-3任一项所述的工艺,其特征在于,镀第一层膜时的氨气与硅烷的气体流量比为3.5~4.5,镀第一层膜时的氨气与硅烷的气体流量比为8.5~9.5。
5.根据权利要求1-4任一项所述的工艺,其特征在于,镀膜时的压力为1650~1705torr。
6.根据权利要求1-5任一项所述的工艺,其特征在于,镀第一层膜时的射频功率为6000~6300W,镀第二层膜时的射频功率为7000~7300W。
7.根据权利要求1-6任一项所述的工艺,其特征在于,镀第一层膜时的脉冲开关比为1/9~1/11,镀第二层膜时的脉冲开关比为1/7~1/9。
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