CN112038426B - 一种晶格失配型三结砷化镓太阳电池及制作方法 - Google Patents

一种晶格失配型三结砷化镓太阳电池及制作方法 Download PDF

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CN112038426B
CN112038426B CN202011226626.6A CN202011226626A CN112038426B CN 112038426 B CN112038426 B CN 112038426B CN 202011226626 A CN202011226626 A CN 202011226626A CN 112038426 B CN112038426 B CN 112038426B
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徐培强
张银桥
王向武
潘彬
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Nanchang Kaixun photoelectric Co.,Ltd.
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Abstract

本发明公开了一种晶格失配型三结砷化镓太阳电池及制作方法,自下向上依次为Ge衬底、底电池、GaAs/InGaAs缓冲层、中底隧穿结、GaAs缓冲层,In(Al)GaAs缓冲层,DBR,中电池、中顶隧穿结、顶电池和盖帽层;其中,In(Al)GaAs缓冲层由InAlAs成核层,InAlAs缓冲层,超晶格,低Al组分InAlGaAs,InGaAs组成;盖帽层由InGaAs和GaAs组成。通过引入InAlGaAs缓冲层,可以有效释放应力和过滤位错,在保证太阳电池材料晶体质量的情况下,使外延材料的晶格常数快速的达到目标值,降低产品生产周期,降低对中底隧穿结的损伤等,同时,通过盖帽层中GaAs的厚度,调节整个外延片的翘曲状况,获得平整的外延片。

Description

一种晶格失配型三结砷化镓太阳电池及制作方法
技术领域
本发明涉及太阳电池技术领域,尤其涉及一种晶格失配型三结砷化镓太阳电池及制作方法。
背景技术
自1957年10月4日起,世界上第一颗人造地球卫星“卫星1号”进入太空以来,在短短几十年里,航天技术取得了巨大的进步,对航天器电源系统的大功率、高可靠性、长寿命和微小型化也提出了新的要求。砷化镓太阳电池具有更高的光电转换效率、更好的耐高温性能、更强的空间抗辐射能力,成功取代Si太阳电池,成为我国航天飞行器,如人造卫星、宇宙飞船、空间实验室等高性能长寿命通用化空间主电源。在国内,经过几代航天人的不断努力,晶格匹配型GaInP/InGaAs/Ge三结太阳电池的转换效率已突破30%,接近半经验理论极限值,很难进一步提高。近年来,禁带匹配,晶格失配的三结太阳电池成为研究的热点,目前已经实现32%效率太阳电池的生产。目前,晶格失配结构太阳电池的结构,主要是通过阶变缓冲层的方式,将晶格常数过渡到目标值,该方法的缺点主要有以下几点:
(1)生产步骤多,生长时间长;
(2)生长过程中的烘烤,降低中底隧穿结性能;
(3)应力释放不完全,容易造成外延片翘曲;
(4)晶体质量不够好。
发明内容
本申请提供了一种晶格失配型三结砷化镓太阳电池及制作方法,通过引入InAlGaAs材料Al组分阶变缓冲层,可以有效释放应力和过滤位错,在保证太阳电池材料晶体质量的情况下,使外延材料的晶格常数快递的达到目标值,降低产品生产周期,降低对中底隧穿结的损伤等,同时,通过盖帽层中GaAs的厚度,调节整个外延片的翘曲状况,获得平整的外延片。
一种晶格失配型三结砷化镓太阳电池,自下向上依次为Ge衬底、底电池、GaAs/InGaAs缓冲层、中底隧穿结、GaAs缓冲层,In(Al)GaAs缓冲层,DBR,中电池、中顶隧穿结、顶电池和盖帽层;其中,In(Al)GaAs缓冲层由InAlAs成核层,InAlAs缓冲层,超晶格,低Al组分InAlGaAs,InGaAs组成;盖帽层由InGaAs和GaAs组成。
一种晶格失配型三结砷化镓太阳电池的制作方法,制作方法步骤如下:
S1:在P型Ge衬底上,高温下通过PH3扩散的形式,形成底电池发射区,然后生长GaInP或AlGaInP成核层,该成核层同时作为底电池的窗口层;
S2:生长GaAs/In0.01GaAs缓冲层,GaAs和In0.01GaAs的厚度分别在0.1-0.8μm;
S3:生长中底隧穿结,中底隧穿结为N++GaAs/P++GaAs结构;
S4:然后生长GaAs缓冲层,GaAs缓冲层厚度为0.2-0.6μm,掺杂浓度大于1×1018/cm3
S5:生长In(Al)GaAs缓冲层,生长顺序依次为预通In,生长InxAlAs成核层,InxAlAs缓冲层,In(x-a)AlAs/In(x+a)AlAs超晶格,Inx(Al)GaAs缓冲层,InyGaAs缓冲层;
S6:生长DBR,DBR由15~30对InyAlGaAs/InyGaAs结构组成, InyAlGaAs层和InyGaAs层的厚度均根据λ/4n计算,其中900nm≤λ≤1100nm,n为对应InAlGaAs或者InGaAs材料的折射率;
S7:生长中电池,中电池材料包括InyGaAs基区和发射区,厚度1.4-2.2μm,AlInP或GaInP窗口层,厚度0.05-0.2μm;
S8:生长中顶隧穿结,中顶隧穿结为N++GaInP/P++InyAlGaAs结构;
S9:生长顶电池,顶电池晶格常数与中电池匹配,由AlGaInP背电场、GaInP基区、GaInP发射区及AlInP窗口层组成;
S10:生长盖帽层,盖帽层由InyGaAs和GaAs组成。
优选的,步骤S1中,发射区厚度为0.1-0.4μm ;GaInP或AlGaInP成核层,厚度0.01-0.03μm。
优选的,步骤S3中,其中N++GaAs的厚度为0.01-0.03μm之间,掺杂浓度为大于1×1019/cm3,掺杂剂为Te、Se、Si其中的一种或者多种组合;P++GaAs的厚度为0.01-0.03μm之间,掺杂浓度大于2×1019/cm3,掺杂剂为Mg、Zn、C其中的一种或者多种组合。
优选的,步骤S5中,预通In,在GaAs缓冲层表面形成一层厚度小于5nm的InAs层;然后成长InxAlAs成核层,成核层厚度0.005-0.02μm;然后生长InxAlAs缓冲层,厚度0.1-0.4μm,In(x-a)AlAs/In(x+a)AlAs超晶格,超晶格总数不超过10对;然后生长Inx(Al)GaAs缓冲层,厚度0.1-0.4μm;然后生长与中电池晶格匹配的InyGaAs缓冲层,厚度0.1-0.3μm,其中0.01≤x≤0.15,0.01≤y≤0.10,0≤a≤0.03,x≥y,x>a。
优选的,步骤S8中,N++GaInP厚度为0.01-0.03μm之间,掺杂浓度为大于1×1019/cm3,掺杂剂为Te、Se、Si其中的一种或者多种组合;P++InyAlGaAs的厚度为0.01-0.03μm之间,掺杂浓度大于2×1019/cm3,掺杂剂为Mg、Zn、C其中的一种或者多种组合。
优选的,步骤S9中,AlGaInP中Al的组分在0.15-0.4之间,厚度在0.02-0.15μm之间,GaInP基区及发射区的总厚度在0.5~1μm之间,AlInP窗口层厚度在0.05~0.1μm之间。
优选的,步骤S10中,InyGaAs厚度在0.3-0.5μm之间,GaAs厚度在0.05-0.3μm之间,通过改变GaAs的厚度,调节外延片翘曲。
有益效果:
预通In技术。在GaAs缓冲层上,先预通In,使In原子分散在GaAs表面,形成密集且均匀分布的小的成核中心,这种密集分散的成核中心及成核岛的合并,可以快速有效的释放应力,然后生长InAlAs成核层,InAlAs成核层的位错密度较高,同样可以快速有效的释放应力;
缓冲层组分阶变技术。先生长一层InAlAs缓冲层,该缓冲层可以进一步的快速释放应力,使得外延层的应力得到充分释放,后续外延材料的生长奠定基础。然后生长一组应变平衡层,采用张、压交替生长的超晶格结构,过滤位错,最后一层低Al组分的InAlGaAs,由于Ga原子迁移率更高,可以获得平整的外延表面;
盖帽层翘曲控制技术。盖帽层由InGaAs和GaAs组成,通过调节GaAs层的厚度,对外延片的整体翘曲进行调节。
附图说明
图1是本发明太阳电池结构图;
图2是本发明In(Al)GaAs缓冲层结构图;
图3是本发明帽盖层结构图。
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。
一种晶格失配型三结砷化镓太阳电池,自下向上依次为Ge衬底、底电池、缓冲层、中底隧穿结、缓冲层,In(Al)GaAs缓冲层,DBR,中电池、中顶隧穿结、顶电池和盖帽层。其中,In(Al)GaAs缓冲层由InAlAs成核层,InAlAs缓冲层,超晶格,低Al组分InAlGaAs,InGaAs组成,盖帽层由InGaAs和GaAs组成。
实施例一:
S1:在P型Ge衬底上,720℃下,通过PH3扩散的形式,形成底电池发射区,发射区厚度为0.1μm,然后温度降低至640℃,生长GaInP成核层,厚度0.01μm,该成核层同时作为底电池的窗口层;
S2:温度提升至650℃,生长GaAs/In0.01GaAs缓冲层,GaAs厚度为0.1μm,In0.01GaAs厚度为0.1μm;
S3:温度降至560℃,生长中底隧穿结,中底隧穿结为N++GaAs/P++GaAs结构,其中N++GaAs的厚度为0.01μm,掺杂浓度为1×1019/cm3,掺杂剂为Te和Si的组合;P++GaAs的厚度为0.01μm,掺杂浓度为2×1019/cm3,掺杂剂为C;
S4:温度提升至650℃,生长GaAs缓冲层,GaAs缓冲层厚度为0.2μm,掺杂浓度为1×1018/cm3
S5:生长In(Al)GaAs缓冲层,依次预通In,生长InxAlAs成核层,InxAlAs缓冲层,In(x-a)AlAs/In(x+a)AlAs超晶格,Inx(Al)GaAs缓冲层,InyGaAs缓冲层。其中预通In,在GaAs缓冲层表面形成一层厚度5nm的InAs层;然后成长In0.01AlAs成核层,成核层厚度0.005μm;然后生长In0.01AlAs缓冲层,厚度0.1μm,In0.01AlAs/In0.01AlAs超晶格,超晶格为10对;然后生长In0.01(Al)GaAs缓冲层,厚度0.1μm;然后生长与中电池晶格匹配的In0.01GaAs缓冲层,厚度0.1μm;
S6:生长DBR。DBR由15对In0.01AlGaAs/In0.01GaAs结构组成,每对In0.01AlGaAs/In0.01GaAs结构中,In0.01AlGaAs层和In0.01GaAs层的厚度均根据λ/4n计算,其中900nm≤λ≤1100nm,n为对应In0.01AlGaAs或者In0.01GaAs材料的折射率;
S7:生长中电池。中电池材料包括In0.01GaAs基区和发射区,厚度1.4μm,GaInP窗口层,厚度0.05μm;
S8:温度降至560℃,生长中顶隧穿结。中顶隧穿结为N++GaInP/P++In0.01AlGaAs结构,其中,N++GaInP厚度为0.01μm,掺杂浓度为1×1019/cm3,掺杂剂为Te和Si的组合;P++In0.01AlGaAs的厚度为0.01μm之间,掺杂浓度为2×1019/cm3,掺杂剂为C;
S9:温度提升至620℃,生长顶电池。顶电池晶格常数与中电池匹配,依次生长Al0.15Ga0.35In0.5P背电场,厚度0.02μm,Ga0.50In0.50P基区和发射区,厚度0.5μm,Al0.50In0.50P窗口层,厚度0.05μm;
S10:生长盖帽层。盖帽层由In0.01GaAs和GaAs组成,其中In0.01GaAs厚度为0.3μm,GaAs厚度为0.05μm。
实施例二:
S1:在P型Ge衬底上,720℃下,通过PH3扩散的形式,形成底电池发射区,发射区厚度为0.3μm,然后温度降低至640℃,生长AlGaInP成核层,厚度0.02μm,该成核层同时作为底电池的窗口层;
S2:温度提升至650℃,生长GaAs/In0.01GaAs缓冲层,GaAs厚度为0.1μm,In0.01GaAs厚度为0.4μm;
S3:温度降至560℃,生长中底隧穿结,中底隧穿结为N++GaAs/P++GaAs结构,其中N++GaAs的厚度为0.02μm,掺杂浓度为3×1019/cm3,掺杂剂为Te和Se的组合;P++GaAs的厚度为0.02μm,掺杂浓度为5×1019/cm3,掺杂剂为Zn;
S4:温度提升至650℃,生长GaAs缓冲层,GaAs缓冲层厚度为0.4μm,掺杂浓度为2×1018/cm3
S5:生长In(Al)GaAs缓冲层,依次预通In,生长InxAlAs成核层,InxAlAs缓冲层,In(x-a)AlAs/In(x+a)AlAs超晶格,Inx(Al)GaAs缓冲层,InyGaAs缓冲层。其中预通In,在GaAs缓冲层表面形成一层厚度5nm的InAs层;然后成长In0.05AlAs成核层,成核层厚度0.01μm;然后生长In0.05AlAs缓冲层,厚度0.2μm,In0.03AlAs/In0.07AlAs超晶格,超晶格为10对;然后生长In0.05(Al)GaAs缓冲层,厚度0.2μm;然后生长与中电池晶格匹配的In0.04GaAs缓冲层,厚度0.2μm;
S6:生长DBR。DBR由25对In0.04AlGaAs/In0.04GaAs结构组成,每对In0.04AlGaAs/In0.04GaAs结构中,In0.04AlGaAs层和In0.04GaAs层的厚度均根据λ/4n计算,其中900nm≤λ≤1100nm,n为对应In0.04AlGaAs或者In0.04GaAs材料的折射率;
S7:生长中电池。中电池材料包括In0.04GaAs基区和发射区,厚度2μm,GaInP窗口层,厚度0.1μm;
S8:温度降至560℃,生长中顶隧穿结。中顶隧穿结为N++GaInP/P++In0.04AlGaAs结构,其中,N++GaInP厚度为0.02μm,掺杂浓度为3×1019/cm3,掺杂剂为Te和Se的组合;P++In0.04AlGaAs的厚度为0.02μm之间,掺杂浓度为5×1019/cm3,掺杂剂为Zn;
S9:温度提升至620℃,生长顶电池。顶电池晶格常数与中电池匹配,依次生长Al0.25Ga0.225In0.525P背电场,厚度0.08μm,Ga0.475In0.525P基区和发射区,厚度0.7μm,Al0.475In0.525P窗口层,厚度0.06μm;
S10:生长盖帽层。盖帽层由In0.04GaAs和GaAs组成,其中In0.04GaAs厚度为0.4μm,GaAs厚度为0.2μm。
实施例三:
S1:在P型Ge衬底上,720℃下,通过PH3扩散的形式,形成底电池发射区,发射区厚度为0.4μm,然后温度降低至640℃,生长GaInP成核层,厚度0.03μm,该成核层同时作为底电池的窗口层;
S2:温度提升至650℃,生长GaAs/In0.01GaAs缓冲层,GaAs厚度为0.8μm,In0.01GaAs厚度为0.8μm;
S3:温度降至560℃,生长中底隧穿结,中底隧穿结为N++GaAs/P++GaAs结构,其中N++GaAs的厚度为0.03μm,掺杂浓度为5×1019/cm3,掺杂剂为Se和Si的组合;P++GaAs的厚度为0.03μm,掺杂浓度为1×1020/cm3,掺杂剂为Mg;
S4:温度提升至650℃,生长GaAs缓冲层,GaAs缓冲层厚度为0.6μm,掺杂浓度为3×1018/cm3
S5:生长In(Al)GaAs缓冲层,依次预通In,生长InxAlAs成核层,InxAlAs缓冲层,In(x-a)AlAs/In(x+a)AlAs超晶格,Inx(Al)GaAs缓冲层,InyGaAs缓冲层。其中预通In,在GaAs缓冲层表面形成一层厚度5nm的InAs层;然后成长In0.15AlAs成核层,成核层厚度0.02μm;然后生长In0.15AlAs缓冲层,厚度0.4μm,In0.12AlAs/In0.18AlAs超晶格,超晶格为10对;然后生长In0.15(Al)GaAs缓冲层,厚度0.4μm;然后生长与中电池晶格匹配的In0.1GaAs缓冲层,厚度0.3μm;
S6:生长DBR。DBR由30对In0.1AlGaAs/In0.1GaAs结构组成,每对In0.1AlGaAs/In0.1GaAs结构中,In0.1AlGaAs层和In0.1GaAs层的厚度均根据λ/4n计算,其中900nm≤λ≤1100nm,n为对应In0.1AlGaAs或者In0.1GaAs材料的折射率;
S7:生长中电池。中电池材料包括In0.1GaAs基区和发射区,厚度2.2μm,GaInP窗口层,厚度0.2μm;
S8:温度降至560℃,生长中顶隧穿结。中顶隧穿结为N++GaInP/P++In0.1AlGaAs结构,其中,N++GaInP厚度为0.03μm,掺杂浓度为5×1019/cm3,掺杂剂为Se和Si的组合;P++In0.1AlGaAs的厚度为0.03μm之间,掺杂浓度为8×1019/cm3,掺杂剂为Mg;
S9:温度提升至620℃,生长顶电池。顶电池晶格常数与中电池匹配,依次生长Al0.4Ga0.02In0.58P背电场,厚度0.15μm,Ga0.42In0.58P基区和发射区,厚度0.1μm,Al0.42In0.58P窗口层,厚度0.1μm;
S10:生长盖帽层。盖帽层由In0.1GaAs和GaAs组成,其中In0.1GaAs厚度为0.5μm,GaAs厚度为0.3μm。
本发明通过预通In技术,在GaAs缓冲层上,先预通In,使In原子分散在GaAs表面,形成密集且均匀分布的小的成核中心,这种密集分散的成核中心及成核岛的合并,可以快速有效的释放应力,然后生长InAlAs成核层,InAlAs成核层的位错密度较高,同样可以快速有效的释放应力。
缓冲层组分阶变技术。先生长一层InAlAs缓冲层,该缓冲层可以进一步的快速释放应力,使得外延层的应力得到充分释放,后续外延材料的生长奠定基础。然后生长一组应变平衡层,采用张、压交替生长的超晶格结构,过滤位错,最后一层低Al组分的InAlGaAs,由于Ga原子迁移率更高,可以获得平整的外延表面。
盖帽层翘曲控制技术。盖帽层由InGaAs和GaAs组成,通过调节GaAs层的厚度,对外延片的整体翘曲进行调节,有效降低了翘曲的问题。

Claims (8)

1.一种晶格失配型三结砷化镓太阳电池,其特征在于:
自下向上依次为Ge衬底、底电池、GaAs/InGaAs缓冲层、中底隧穿结、GaAs缓冲层,In(Al)GaAs缓冲层,DBR,中电池、中顶隧穿结、顶电池和盖帽层;
其中,In(Al)GaAs缓冲层由InAlAs成核层,InAlAs缓冲层,超晶格,低Al组分InAlGaAs,InGaAs组成;
盖帽层由InGaAs和GaAs组成。
2.一种晶格失配型三结砷化镓太阳电池的制作方法,其特征在于,制作方法步骤如下:
S1:在P型Ge衬底上,高温下通过PH3扩散的形式,形成底电池发射区,然后生长GaInP或AlGaInP成核层,该成核层同时作为底电池的窗口层;
S2:生长GaAs/In0.01GaAs缓冲层,GaAs和In0.01GaAs的厚度分别在0.1-0.8μm;
S3:生长中底隧穿结,中底隧穿结为N++GaAs/P++GaAs结构;
S4:然后生长GaAs缓冲层,GaAs缓冲层厚度为0.2-0.6μm,掺杂浓度大于1×1018/cm3
S5:生长In(Al)GaAs缓冲层,生长顺序依次为预通In,生长InxAlAs成核层,InxAlAs缓冲层,In(x-a)AlAs/In(x+a)AlAs超晶格,Inx(Al)GaAs缓冲层,InyGaAs缓冲层;
S6:生长DBR,DBR由15~30对InyAlGaAs/InyGaAs结构组成, InyAlGaAs层和InyGaAs层的厚度均根据λ/4n计算,其中900nm≤λ≤1100nm,n为对应InAlGaAs或者InGaAs材料的折射率;
S7:生长中电池,中电池材料包括InyGaAs基区和发射区,厚度1.4-2.2μm,AlInP或GaInP窗口层,厚度0.05-0.2μm;
S8:生长中顶隧穿结,中顶隧穿结为N++GaInP/P++InyAlGaAs结构;
S9:生长顶电池,顶电池晶格常数与中电池匹配,由AlGaInP背电场、GaInP基区、GaInP发射区及AlInP窗口层组成;
S10:生长盖帽层,盖帽层由InyGaAs和GaAs组成。
3.根据权利要求2所述的一种晶格失配型三结砷化镓太阳电池的制作方法,其特征在于:
步骤S1中,发射区厚度为0.1-0.4μm之间;
GaInP或AlGaInP成核层,厚度0.01-0.03μm之间。
4.根据权利要求2所述的一种晶格失配型三结砷化镓太阳电池的制作方法,其特征在于:
步骤S3中,其中N++GaAs的厚度为0.01-0.03μm之间,掺杂浓度为大于1×1019/cm3,掺杂剂为Te、Se、Si其中的一种或者多种组合;
P++GaAs的厚度为0.01-0.03μm之间,掺杂浓度大于2×1019/cm3,掺杂剂为Mg、Zn、C其中的一种或者多种组合。
5.根据权利要求2所述的一种晶格失配型三结砷化镓太阳电池的制作方法,其特征在于:
步骤S5中,预通In,在GaAs缓冲层表面形成一层厚度小于5nm的InAs层;
然后成长InxAlAs成核层,成核层厚度0.005-0.02μm;
然后生长InxAlAs缓冲层,厚度0.1-0.4μm,In(x-a)AlAs/In(x+a)AlAs超晶格,超晶格总数不超过10对;
然后生长Inx(Al)GaAs缓冲层,厚度0.1-0.4μm;
然后生长与中电池晶格匹配的InyGaAs缓冲层,厚度0.1-0.3μm,其中0.01≤x≤0.15,0.01≤y≤0.10,0≤a≤0.03,x≥y,x>a。
6.根据权利要求2所述的一种晶格失配型三结砷化镓太阳电池的制作方法,其特征在于:
步骤S8中,N++GaInP厚度为0.01-0.03μm之间,掺杂浓度为大于1×1019/cm3,掺杂剂为Te、Se、Si其中的一种或者多种组合;
P++InyAlGaAs的厚度为0.01-0.03μm之间,掺杂浓度大于2×1019/cm3,掺杂剂为Mg、Zn、C其中的一种或者多种组合。
7.根据权利要求2所述的一种晶格失配型三结砷化镓太阳电池的制作方法,其特征在于:
步骤S9中,AlGaInP中Al的组分在0.15-0.4之间,厚度在0.02-0.15μm之间,GaInP基区及发射区的总厚度在0.5~1μm之间,AlInP窗口层厚度在0.05~0.1μm之间。
8.根据权利要求2所述的一种晶格失配型三结砷化镓太阳电池的制作方法,其特征在于:
步骤S10中,InyGaAs厚度在0.3-0.5μm之间,GaAs厚度在0.05-0.3μm之间,通过改变GaAs的厚度,调节外延片翘曲。
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