CN108281496A - 一种硅基PiN紫外光电二极管及其制备方法 - Google Patents
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- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title claims abstract description 51
- 229910052710 silicon Inorganic materials 0.000 title claims abstract description 51
- 239000010703 silicon Substances 0.000 title claims abstract description 51
- 239000000758 substrate Substances 0.000 title claims abstract description 41
- 238000002360 preparation method Methods 0.000 title claims abstract description 17
- 229910000480 nickel oxide Inorganic materials 0.000 claims abstract description 51
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 claims abstract description 51
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 31
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 15
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 13
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 13
- 238000001755 magnetron sputter deposition Methods 0.000 claims abstract description 13
- 239000004411 aluminium Substances 0.000 claims abstract description 12
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 28
- 238000000151 deposition Methods 0.000 claims description 23
- 230000008021 deposition Effects 0.000 claims description 19
- 238000000137 annealing Methods 0.000 claims description 16
- 238000004544 sputter deposition Methods 0.000 claims description 16
- 229910052786 argon Inorganic materials 0.000 claims description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 14
- 239000001301 oxygen Substances 0.000 claims description 14
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 238000004062 sedimentation Methods 0.000 claims description 11
- 238000004140 cleaning Methods 0.000 claims description 9
- 238000005137 deposition process Methods 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 6
- 230000008859 change Effects 0.000 claims description 2
- 230000004044 response Effects 0.000 abstract description 8
- 239000010408 film Substances 0.000 description 42
- 239000008367 deionised water Substances 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 8
- 238000001771 vacuum deposition Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
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- 238000000034 method Methods 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VVTSZOCINPYFDP-UHFFFAOYSA-N [O].[Ar] Chemical compound [O].[Ar] VVTSZOCINPYFDP-UHFFFAOYSA-N 0.000 description 1
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- 229910021645 metal ion Inorganic materials 0.000 description 1
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Abstract
本发明公开了一种硅基PiN紫外光电二极管,包括铝电极和镍电极,两电极之间依次附有N型硅衬底、i层氧化镍薄膜和P型氧化镍薄膜。其制备方法是采用磁控溅射设备,利用氧化镍在硅上沉积成膜,形成PiN异质结结构,氧化镍薄膜可作为紫外光吸收层,解决了硅器件的紫外响应问题,制备过程简单易行。
Description
技术领域
本发明属于可扩展硅光控二极管技术领域,具体涉及一种硅基PiN紫外光电二极管及其制备方法。
背景技术
硅在近紫外到近红外区有较高的灵敏度,但由于其频带(1.12eV)的限制,只限于在1.1μm波长以下使用,限制在紫外光电领域的发展,与红外、可见光波段探测相比,半导体紫外光电探测器有以下优点:对可见及红外波段是“可见盲”或“日盲”,可以防止太阳光及其它可见光、红外光等自然光源的干扰,结构简单、响应速度快、可靠性高、体积小等。为了使硅基光电器件可受控于紫外光源,在硅衬底上制备NiO薄膜,NiO是直接宽带隙半导体材料,不仅在发光器件应用方面有独特的优势,而且作为探测器可以实现窄的波长响应和较高的光谱响应度。2017年,Bhaskar Parida,Seongjun Kim等在论文《Nanostructured-NiO/Si heterojunction photodector》中采用了溶胶凝胶法制备了NiO/Si异质结,结果表明异质结具有良好的整流特性,且具有一定的光响应,但响应速度较低。
发明内容
本发明的目的是提供一种硅基PiN结构紫外光电二极管,解决了硅基光电器件紫外光控问题。
本发明另一目的是提供该二极管的制备方法。
本发明所采用的一个技术方案是,一种硅基PiN紫外光电二极管,包括铝电极和镍电极,两电极之间由铝电极向镍电极方向依次附有N型硅衬底、i层氧化镍薄膜和P型氧化镍薄膜。
优选地,上述i层氧化镍薄膜厚度为30nm-100nm,P型氧化镍薄膜厚度为30nm-100nm。
本发明所采用的另一个技术方案是,上述硅基PiN紫外光电二极管的制备方法,包括以下步骤:
(1)对N型硅衬底进行RCA清洗;
(2)利用磁控溅射设备,在N型硅衬底上沉积出i层氧化镍薄膜;
(3)利用磁控溅射设备,在i层氧化镍薄膜上沉积出P型氧化镍薄膜;
(4)在P型氧化镍薄膜上沉积镍电极;
(5)在硅片背面沉积铝电极;
(6)退火,形成欧姆接触。
优选地,上述i层氧化镍薄膜的沉积工艺为:沉积过程只通入氩气,沉积时间控制为0.1h-2h,沉积压强控制为1Pa-5Pa,溅射功率控制为80W-160W。溅射时间决定了i层厚度,溅射压强影响镀膜速率,功率影响沉积薄膜的质量,在此范围内,能得到具有较高紫外光响应度的i层氧化镍薄膜。
优选地,上述P型氧化镍薄膜的沉积工艺为:沉积过程中同时通入氩气和氧气,二者流量比为1:1,沉积时间控制为0.1h-2h,沉积压强控制为1Pa-5Pa,溅射功率控制为80W-160W。溅射时间决定了p型氧化镍厚度,溅射压强影响镀膜速率,功率影响沉积薄膜的质量,在此范围内,能得到具有较高紫外光响应度的P层氧化镍薄膜。氩气流量和氧气流量比为1:1时,所形成的P型氧化镍薄膜结晶质量最好。
优选地,上述退火温度为400℃-600℃,退火时间为60S-500S。
本发明技术方案的原理是,硅在近紫外到近红外区有较高的灵敏度,但由于其频带(1.12eV)的限制,只限于在1.1μm波长以下使用,限制在紫外光电领域的发展,而NiO薄膜是直接宽带隙半导体材料,不仅在发光器件应用方面有独特的优势,而且作为探测器可以实现窄的波长响应和较高的光谱响应度。利用氧化镍来吸收紫外光,当紫外光照射半导体时,当入射光子能量大于或等于材料的禁带宽度时,就被半导体吸收,并激发P区、i区和N区的价带电子,产生光生电子-空穴对,电场作用使电子空穴分离,导带中电子向N区移动,价带中空穴向P区移动,在器件两端产生光电压,在外电路中形成光电流,将接收到的光信号转换为电信号输出,实现光电转换。
本发明的硅基PiN结构紫外光电二极管的制备方法,利用氧化镍在硅上沉积成膜,形成PiN异质结结构,解决了硅器件的紫外响应问题,制备过程简单易行。
附图说明
图1是本发明硅基PiN结构紫外光电二极管示意图;
图2是本发明硅基PiN结构紫外光电二极管的制备方法流程示意图;
图3是本发明p型NiO薄膜在不同氩氧比的条件下XRD图谱;
图4是本发明硅基PiN结构紫外光电二极管的开关特性。
具体实施方式
下面结合附图和具体实施方式对本发明作进一步的详细说明,但本发明并不限于这些实施方式。
本发明的硅基PiN紫外光电二极管一种具体结构如图1所示,包括二极管两端的铝电极和镍叉指状电极,两电极之间由铝电极向镍电极方向依次附有N型单晶硅衬底、i层氧化镍薄膜和P型氧化镍薄膜。
其中,i层氧化镍薄膜厚度为30nm-100nm,P型氧化镍薄膜厚度为30nm-100nm。
通过上述成膜搭配,形成P-i-N异质结结构,N为N型单晶硅衬底,i为i层氧化镍薄膜,P为P型氧化镍薄膜,氧化镍薄膜可作为紫外光吸收层,解决硅器件的紫外响应问题。
如图2所示,本发明的硅基PiN紫外光电二极管的制备方法如下:
(1)对N型硅衬底进行RCA清洗,
1、首先将硅衬底用去离子水冲洗清;
2、在丙酮溶液中超声清洗15min,用来去除衬底表面的有机杂质,再用去离子水冲洗;
3、按照氨水:过氧化氢:去离子水=1:1:4配比配置标准一号溶液,在80℃水浴中加热15min,用来去除金属离子及有机杂质,再用去离子水冲洗;
4、按照盐酸:过氧化氢:去离子水=1:1:5配比配置标准二号溶液,在80℃水浴中加热15min,再用去离子水冲洗;
5、在10%的氢氟酸溶液中浸泡10min,用来去除Si表面的氧化层,再用去离子水冲洗;
6、在无水乙醇中超声清洗15min,再用去离子水冲洗,最后用N2吹干
(2)利用磁控溅射设备在N型硅衬底上沉积出i层氧化镍薄膜,沉积过程中只通入氩气,不通入氧气,沉积时间控制为0.1h-2h,沉积压强控制为1Pa-5Pa,溅射功率控制为80W-160W。
(3)利用磁控溅射设备,在i层氧化镍薄膜上沉积出P型氧化镍薄膜,沉积过程中同时通入氩气和氧气,沉积时间控制为0.1h-2h,沉积压强控制为1Pa-5Pa,溅射功率控制为80W-160W。其中,氩气流量和氧气流量比为1:1时,所形成的P型氧化镍薄膜结晶质量最好(如图3所示)。
(4)利用真空镀膜设备,蒸发源为Ni粉,真空度为5×10-3Pa,使用叉指状掩膜版,在P型氧化镍薄膜上沉积镍叉指状电极。
(5)利用真空镀膜设备,蒸发源为Al粒,真空度为5×10-3Pa,在硅片背面沉积铝电极。
(6)使用快速退火设备对步骤5得到的样品进行退火以形成欧姆接触,退火温度为400℃-600℃,退火时间为60S-500S。
图4为所制备紫外光电二极管在纯电阻负载电路中的电压开关波形,测试用光源信号来自365nm紫外LED,连续紫外光经斩波器转化为方波信号,测试结果表明,本发明所制备的器件在365nm紫外光控制下具有良好的开关性能。
以下给出具体制备实施例,通过以下方法均可制备出本发明的硅基PiN紫外光电二极管。
实施例1
对N型单晶硅衬底进行RCA清洗,清洗后用氮气吹干待用。采用磁控溅射设备在硅衬底上沉积100nm厚的i层氧化镍薄膜,氩气流量为20sccm,氧气流量为0sccm,沉积时间为2h,沉积压强为1Pa,溅射功率控制为100W。再采用磁控溅射设备沉积100nm厚的P型氧化镍薄膜,氩气流量为20sccm,氧气流量为20sccm,沉积时间为2h,沉积压强为1Pa,溅射功率控制为100W。再利用真空镀膜设备在P型氧化镍薄膜上沉积镍叉指状电极。再利用真空镀膜设备在硅片背面沉积铝电极。最后使用快速退火设备对样品进行退火以形成欧姆接触,退火温度450℃,退火时间180s。
实施例2
对N型单晶硅衬底进行RCA清洗,清洗后用氮气吹干待用。采用磁控溅射设备在硅衬底上沉积100nm厚的i层氧化镍薄膜,氩气流量为20sccm,氧气流量为0sccm,沉积时间为3h,沉积压强为1Pa,溅射功率控制为100W。再采用磁控溅射设备沉积100nm厚的P型氧化镍薄膜,氩气流量为40sccm,氧气流量为20sccm,沉积时间为1h,沉积压强为1Pa,溅射功率控制为100W。再利用真空镀膜设备在P型氧化镍薄膜上沉积镍叉指状电极。再利用真空镀膜设备在硅片背面沉积铝电极。最后使用快速退火设备对样品进行退火以形成欧姆接触,退火温度450℃,退火时间180s。
实施例3
对N型单晶硅衬底进行RCA清洗,清洗后用氮气吹干待用。采用磁控溅射设备在硅衬底上沉积100nm厚的i层氧化镍薄膜,氩气流量为20sccm,氧气流量为0sccm,沉积时间为1h,沉积压强为1Pa,溅射功率控制为100W。再采用磁控溅射设备沉积100nm厚的P型氧化镍薄膜,氩气流量为20sccm,氧气流量为40sccm,沉积时间为3h,沉积压强为1Pa,溅射功率控制为100W。再利用真空镀膜设备在P型氧化镍薄膜上沉积镍叉指状电极。再利用真空镀膜设备在硅片背面沉积铝电极。最后使用快速退火设备对样品进行退火以形成欧姆接触,退火温度450℃,退火时间180s。
Claims (7)
1.一种硅基PiN紫外光电二极管,其特征在于,包括铝电极和镍电极,两电极之间由铝电极向镍电极方向依次附有N型硅衬底、i层氧化镍薄膜和P型氧化镍薄膜。
2.根据权利要求1所述的硅基PiN紫外光电二极管,其特征在于,所述i层氧化镍薄膜厚度为30nm-100nm,P型氧化镍薄膜厚度为30nm-100nm。
3.一种如权利要求1所述的硅基PiN紫外光电二极管的制备方法,其特征在于,包括以下步骤:
(1)对N型硅衬底进行RCA清洗;
(2)利用磁控溅射设备,在N型硅衬底上沉积出i层氧化镍薄膜;
(3)利用磁控溅射设备,在i层氧化镍薄膜上沉积出P型氧化镍薄膜;
(4)在P型氧化镍薄膜上沉积镍电极;
(5)在硅片背面沉积铝电极;
(6)退火,形成欧姆接触。
4.根据权利要求3所述的硅基PiN紫外光电二极管的制备方法,其特征在于,步骤(2)所述i层氧化镍薄膜的沉积工艺为:沉积过程只通入氩气,沉积时间控制为0.1h-2h,沉积压强控制为1Pa-5Pa,溅射功率控制为80W-160W。
5.根据权利要求3所述的硅基PiN紫外光电二极管的制备方法,其特征在于,步骤(3)所述P型氧化镍薄膜的沉积工艺为:沉积过程中同时通入氩气和氧气,二者流量比为1:1,沉积时间控制为0.1h-2h,沉积压强控制为1Pa-5Pa,溅射功率控制为80W-160W。
6.根据权利要求3所述的硅基PiN紫外光电二极管的制备方法,其特征在于,步骤(6)所述退火温度为400℃-600℃,退火时间为60S-500S。
7.根据权利要求3所述的硅基PiN紫外光电二极管的制备方法,其特征在于,所述i层氧化镍薄膜厚度为30nm-100nm,P型氧化镍薄膜厚度为30nm-100nm。
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