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CN106784320A - Based on CH3NH3PbI3Reflective enhancing N-type hetero-junctions HEMT of substrate of material and preparation method thereof - Google Patents

Based on CH3NH3PbI3Reflective enhancing N-type hetero-junctions HEMT of substrate of material and preparation method thereof Download PDF

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CN106784320A
CN106784320A CN201611124458.3A CN201611124458A CN106784320A CN 106784320 A CN106784320 A CN 106784320A CN 201611124458 A CN201611124458 A CN 201611124458A CN 106784320 A CN106784320 A CN 106784320A
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pbi
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substrate
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CN106784320B (en
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贾仁需
刘银涛
汪钰成
庞体强
张玉明
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Xidian University
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    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
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    • H10K30/00Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
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    • H10K30/65Light-sensitive field-effect devices, e.g. phototransistors
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K71/00Manufacture or treatment specially adapted for the organic devices covered by this subclass
    • H10K71/10Deposition of organic active material
    • H10K71/12Deposition of organic active material using liquid deposition, e.g. spin coating
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K77/00Constructional details of devices covered by this subclass and not covered by groups H10K10/80, H10K30/80, H10K50/80 or H10K59/80
    • H10K77/10Substrates, e.g. flexible substrates
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Abstract

本发明涉及一种基于CH3NH3PbI3材料的衬底反光增强N型异质结HEMT及其制备方法。该方法包括:选取蓝宝石衬底;在衬底下表面形成反光层;在衬底上表面制作源漏电极;在衬底上表面形成电子传输层;在电子传输层表面形成包括CH3NH3PbI3材料的光吸收层;在光吸收层表面制作栅电极以最终形成N型异质结HEMT。本发明采用由CH3NH3PbI3向沟道提供大量的电子,在衬底下表面镀银形成反射增强型HEMT,具有迁移率高,开关速度快,光吸收以及光利用率增强,光生载流子增多,光电转换效率大的优点。另外,采用在光吸收层加入了PCBM材料形成了异质结,能通过对孔洞和空位的填充改善光吸收层薄膜的质量,从而产生更大的晶粒和更少的晶界,吸收更多的光产生光生载流子,增强器件性能。

The invention relates to a substrate light reflection enhanced N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 material and a preparation method thereof. The method includes: selecting a sapphire substrate; forming a light-reflecting layer on the lower surface of the substrate; making source-drain electrodes on the upper surface of the substrate; forming an electron transport layer on the upper surface of the substrate ; A light-absorbing layer of the material; a gate electrode is fabricated on the surface of the light-absorbing layer to finally form an N-type heterojunction HEMT. The present invention uses CH 3 NH 3 PbI 3 to provide a large number of electrons to the channel, and silver-plates the lower surface of the substrate to form a reflection-enhanced HEMT, which has high mobility, fast switching speed, enhanced light absorption and light utilization, and photogenerated current carrying. The number of electrons increases and the photoelectric conversion efficiency is high. In addition, the PCBM material is added to the light absorbing layer to form a heterojunction, which can improve the quality of the light absorbing layer film by filling holes and vacancies, resulting in larger grains and fewer grain boundaries, absorbing more The light generates photogenerated carriers and enhances the device performance.

Description

基于CH3NH3PbI3材料的衬底反光增强N型异质结HEMT及其制备 方法Substrate reflection-enhanced N-type heterojunction HEMT based on CH3NH3PbI3 material and its preparation method

技术领域technical field

本发明属于集成电路技术领域,具体涉及一种基于CH3NH3PbI3材料的衬底反光增强N型异质结HEMT及其制备方法。The invention belongs to the technical field of integrated circuits, and in particular relates to a CH 3 NH 3 PbI 3 material-based substrate light reflection enhanced N-type heterojunction HEMT and a preparation method thereof.

背景技术Background technique

随着电子技术的蓬勃发展,半导体集成电路对社会发展和国民经济所起的作用越来越大。而其中市场对光电高速器件的需求与日俱增,并对器件的性能不断提出更高更细致的要求。为寻求突破,不管从工艺,材料还是结构等方面的研究一直未有间断。近年来,随着可见光无线通讯技术以及电路耦合技术的崛起,市场对可见光波段的光电高电子迁移率晶体管(High Electron Mobility Transistor,简称HEMT)提出了新的要求。With the vigorous development of electronic technology, semiconductor integrated circuits play an increasingly important role in social development and national economy. Among them, the market demand for optoelectronic high-speed devices is increasing day by day, and higher and more detailed requirements are constantly put forward for the performance of the devices. In order to seek a breakthrough, no matter from the aspects of technology, material or structure, the research has been uninterrupted. In recent years, with the rise of visible light wireless communication technology and circuit coupling technology, the market has put forward new requirements for optoelectronic high electron mobility transistors (High Electron Mobility Transistor, HEMT) in the visible light band.

有机/无机钙钛矿(CH3NH3PbI3)的横空出世,又给研究带来了新的视角。有机/无机钙钛矿中的有机基团和无机基团的有序结合,得到了长程有序的晶体结构,并兼具了有机和无机材料的优点。无机组分的高迁移率赋予了杂化钙钛矿良好的电学特性;有机组分的自组装和成膜特性,使得杂化钙钛矿薄膜的制备工艺简单而且低成本,也能够在室温下进行。杂化钙钛矿本身高的光吸收系数也是杂化钙钛矿能够在光电材料中应用的资本。The emergence of organic/inorganic perovskite (CH 3 NH 3 PbI 3 ) has brought a new perspective to the research. The orderly combination of organic and inorganic groups in organic/inorganic perovskites leads to long-range ordered crystal structures that combine the advantages of both organic and inorganic materials. The high mobility of the inorganic component endows the hybrid perovskite with good electrical properties; the self-assembly and film-forming properties of the organic component make the preparation process of the hybrid perovskite film simple and low-cost, and can also be prepared at room temperature conduct. The high light absorption coefficient of hybrid perovskite itself is also the capital that hybrid perovskite can be used in optoelectronic materials.

然后,当前CH3NH3PbI3材料并未很成熟地应用于HMET器件中,而且如何进一步提高光电转换效率仍然是亟待解决的难题。However, the current CH 3 NH 3 PbI 3 material has not been maturely used in HMET devices, and how to further improve the photoelectric conversion efficiency is still an urgent problem to be solved.

发明内容Contents of the invention

为了解决现有技术中存在的上述问题,本发明提供了一种基于CH3NH3PbI3材料的衬底反光增强N型异质结HEMT及其制备方法。In order to solve the above-mentioned problems in the prior art, the present invention provides a CH 3 NH 3 PbI 3 material-based substrate light reflection enhanced N-type heterojunction HEMT and a preparation method thereof.

本发明的一个实施例提供了一种基于CH3NH3PbI3材料的衬底反光增强N型异质结HEMT的制备方法,包括:An embodiment of the present invention provides a method for preparing a CH 3 NH 3 PbI 3 material-based substrate reflection-enhanced N-type heterojunction HEMT, including:

选取蓝宝石衬底;Select the sapphire substrate;

在所述蓝宝石衬底下表面形成反光层;forming a reflective layer on the lower surface of the sapphire substrate;

在所述蓝宝石衬底上表面制作源漏电极;Making source and drain electrodes on the upper surface of the sapphire substrate;

在所述源漏电极以及未被所述源漏电极覆盖的所述蓝宝石衬底上表面形成电子传输层;forming an electron transport layer on the source-drain electrodes and the upper surface of the sapphire substrate not covered by the source-drain electrodes;

在所述电子传输层表面形成包括CH3NH3PbI3材料的光吸收层;forming a light absorbing layer comprising CH 3 NH 3 PbI 3 material on the surface of the electron transport layer;

在所述光吸收层表面制作栅电极以最终形成所述N型异质结HEMT。A gate electrode is formed on the surface of the light absorbing layer to finally form the N-type heterojunction HEMT.

在本发明的一个实施例中,在所述蓝宝石衬底下表面形成反光层,包括:In one embodiment of the present invention, a reflective layer is formed on the lower surface of the sapphire substrate, comprising:

以Ag材料作为靶材,以Ar作为溅射气体通入溅射腔,在真空度为6×10-4~1.3×10-3Pa,溅射功率为20~100W的条件下,利用磁控溅射工艺,在所述蓝宝石衬底下表面溅射Ag材料形成所述反光层。Using Ag material as the target material, Ar as the sputtering gas into the sputtering chamber, under the conditions of vacuum degree of 6×10 -4 ~ 1.3×10 -3 Pa, sputtering power of 20 ~ 100W, using magnetron Sputtering process, sputtering Ag material on the lower surface of the sapphire substrate to form the reflective layer.

在本发明的一个实施例中,在所述蓝宝石衬底上表面制作源漏电极,包括:In one embodiment of the present invention, making source and drain electrodes on the upper surface of the sapphire substrate includes:

采用第一物理掩膜版,以Au材料作为靶材,以Ar作为溅射气体通入溅射腔,在真空度为6×10-4~1.3×10-3Pa,溅射功率为20~100W的条件下,在所述蓝宝石衬底上表面溅射Au材料形成所述源漏电极。The first physical mask is used, Au material is used as the target material, Ar is used as the sputtering gas to pass into the sputtering chamber, the vacuum degree is 6×10 -4 ~ 1.3×10 -3 Pa, and the sputtering power is 20~ Under the condition of 100W, Au material is sputtered on the upper surface of the sapphire substrate to form the source and drain electrodes.

在本发明的一个实施例中,在所述源漏电极以及未被所述源漏电极覆盖的所述蓝宝石衬底上表面形成电子传输层,包括:In one embodiment of the present invention, an electron transport layer is formed on the source-drain electrodes and the upper surface of the sapphire substrate not covered by the source-drain electrodes, including:

以TiO2材料作为靶材,以Ar和O2作为溅射气体通入溅射腔,在真空度为1.3×10-3~3×10-3Pa,溅射功率为60~80W的条件下,在包括所述源漏电极的整个衬底的上表面溅射TiO2材料形成所述源所述电子传输层。Using TiO 2 material as the target material, Ar and O 2 as the sputtering gas into the sputtering chamber, under the conditions of vacuum degree of 1.3×10 -3 ~ 3×10 -3 Pa and sputtering power of 60 ~ 80W , sputtering TiO 2 material on the upper surface of the entire substrate including the source and drain electrodes to form the source and the electron transport layer.

在本发明的一个实施例中,在所述电子传输层表面形成包括CH3NH3PbI3材料的光吸收层,包括:In one embodiment of the present invention, a light absorbing layer comprising CH 3 NH 3 PbI 3 material is formed on the surface of the electron transport layer, including:

利用单一旋涂工艺,在所述电子传输层表面旋涂质量浓度为8mg/ml的PCBM材料,退火处理后形成活性层;Using a single spin-coating process, spin-coat a PCBM material with a mass concentration of 8 mg/ml on the surface of the electron transport layer, and form an active layer after annealing;

利用单一旋涂工艺,在所述活性层表面旋涂CH3NH3PbI3材料;Spin-coating CH 3 NH 3 PbI 3 material on the surface of the active layer by using a single spin-coating process;

利用退火工艺,对所述CH3NH3PbI3材料进行退火处理形成所述光吸收层。Using an annealing process, the CH 3 NH 3 PbI 3 material is annealed to form the light absorbing layer.

在本发明的一个实施例中,在所述电子传输层表面形成包括CH3NH3PbI3材料的光吸收层,包括:In one embodiment of the present invention, a light absorbing layer comprising CH 3 NH 3 PbI 3 material is formed on the surface of the electron transport layer, including:

利用单一旋涂工艺,将CH3NH3PbI3与PCBM的混合溶液旋涂在所述电子传输层表面形成CH3NH3PbI3/PCBM材料;Using a single spin coating process, spin coating a mixed solution of CH 3 NH 3 PbI 3 and PCBM on the surface of the electron transport layer to form a CH 3 NH 3 PbI 3 /PCBM material;

利用退火工艺,对所述CH3NH3PbI3/PCBM材料进行退火处理形成所述光吸收层。Using an annealing process, the CH 3 NH 3 PbI 3 /PCBM material is annealed to form the light absorbing layer.

在本发明的一个实施例中,将CH3NH3PbI3与PCBM的混合溶液旋涂在所述电子传输层表面形成CH3NH3PbI3/PCBM材料,包括:In one embodiment of the present invention, a mixed solution of CH 3 NH 3 PbI 3 and PCBM is spin-coated on the surface of the electron transport layer to form a CH 3 NH 3 PbI 3 /PCBM material, including:

将PbI2材料和CH3NH3I材料先后加入DMSO:GBL溶液中形成PbI2和CH3NH3I的混合溶液;Add PbI 2 material and CH 3 NH 3 I material to DMSO:GBL solution successively to form a mixed solution of PbI 2 and CH 3 NH 3 I;

将所述PbI2和CH3NH3I的混合溶液加热搅拌,并进行退火处理后形成CH3NH3PbI3溶液;heating and stirring the mixed solution of PbI 2 and CH 3 NH 3 I, and performing annealing treatment to form a CH 3 NH 3 PbI 3 solution;

将所述CH3NH3PbI3溶液和PCBM溶液混合后旋涂在所述电子传输层表面形成所述CH3NH3PbI3/PCBM材料。The CH 3 NH 3 PbI 3 solution and the PCBM solution are mixed and then spin-coated on the surface of the electron transport layer to form the CH 3 NH 3 PbI 3 /PCBM material.

在本发明的一个实施例中,在所述光吸收层表面制作栅电极,包括:In one embodiment of the present invention, fabricating a gate electrode on the surface of the light absorbing layer includes:

采用第二掩膜板,以Au材料作为靶材,以Ar气体作为溅射气体通入溅射腔,在真空度为6×10-4~1.3×10-3Pa,溅射功率为20~100W的条件下,在所述光吸收层表面溅射Au材料形成所述栅电极。Use the second mask plate, use Au material as the target material, and use Ar gas as the sputtering gas to pass into the sputtering chamber. The vacuum degree is 6×10 -4 ~ 1.3×10 -3 Pa, and the sputtering power is 20~ Under the condition of 100W, Au material is sputtered on the surface of the light absorbing layer to form the gate electrode.

本发明的另一个实施例提供了一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT,其中,所述N型异质结HEMT由上述实施例中任一所述的方法制备形成。Another embodiment of the present invention provides an N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 material with enhanced light reflection of the substrate, wherein the N-type heterojunction HEMT is composed of any one of the above-mentioned embodiments Prepared by the method described above.

本发明实施例提供的N型异质结HEMT,具备如下优点:The N-type heterojunction HEMT provided by the embodiment of the present invention has the following advantages:

1、由于本发明的晶体管采用衬底背面镀反光层,把反射光也利用起来,增加了对光的利用率,能吸收更多的光产生光生载流子,增强器件性能。1. Since the transistor of the present invention uses a reflective layer on the back of the substrate, the reflected light is also utilized, which increases the utilization rate of light, absorbs more light to generate photogenerated carriers, and enhances device performance.

2、由于本发明的晶体管采用在光吸收层加入了PCBM材料形成了异质结,能通过对孔洞和空位的填充改善光吸收层薄膜的质量,从而产生更大的晶粒和更少的晶界,吸收更多的光产生光生载流子,增强器件性能。或者,在光吸收层与电子传输层之间加入了PCBM材料,能通过钝化层之间的界面缺陷进而改善光吸收层薄膜的质量,增强器件性能。2. Since the transistor of the present invention forms a heterojunction by adding PCBM material to the light-absorbing layer, the quality of the light-absorbing layer film can be improved by filling holes and vacancies, thereby producing larger crystal grains and fewer crystal grains. Boundary, absorb more light to generate photogenerated carriers, and enhance device performance. Alternatively, the PCBM material is added between the light absorbing layer and the electron transport layer, which can improve the quality of the light absorbing layer film and enhance device performance through the interface defects between the passivation layers.

3、由于本发明的晶体管采用的电子传输层传输电子阻挡空穴,能传输更多的电子,增强器件性能。3. Since the electron transport layer used in the transistor of the present invention transports electrons and blocks holes, more electrons can be transported and the performance of the device can be enhanced.

4、本发明的晶体管采用由CH3NH3PbI3向沟道提供大量的电子,形成衬底镀银反射增强型HEMT高电子迁移率晶体管,具有迁移率高,开关速度快,光吸收以及光利用率增强,光生载流子增多,传输特性增强,光电转换效率大的优点。4. The transistor of the present invention uses CH 3 NH 3 PbI 3 to provide a large amount of electrons to the channel to form a substrate silver-plated reflection-enhanced HEMT high electron mobility transistor, which has high mobility, fast switching speed, light absorption and light absorption. The utilization rate is enhanced, the photogenerated carriers are increased, the transmission characteristics are enhanced, and the photoelectric conversion efficiency is large.

附图说明Description of drawings

图1为本发明实施例提供的一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的截面示意图;Fig. 1 is a schematic cross-sectional view of an N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 materials provided by an embodiment of the present invention with enhanced substrate light reflection;

图2为本发明实施例提供的一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的俯视示意图;Fig. 2 is a schematic top view of an N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 material provided by an embodiment of the present invention with enhanced substrate light reflection;

图3为本发明实施例提供的另一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的截面示意图;3 is a schematic cross-sectional view of another N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 materials provided by an embodiment of the present invention with enhanced substrate light reflection;

图4为本发明实施例提供的一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的制备方法流程示意图;Fig. 4 is a schematic flowchart of a preparation method of an N-type heterojunction HEMT based on a CH 3 NH 3 PbI 3 material provided by an embodiment of the present invention with enhanced reflection of the substrate;

图5a-图5f为本发明实施例提供的一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的制备方法示意图;5a-5f are schematic diagrams of a method for preparing an N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 materials provided by an embodiment of the present invention with enhanced light reflection on the substrate;

图6a-图6g为本发明实施例提供的另一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的制备方法示意图;6a-6g are schematic diagrams of another method for preparing an N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 materials provided by an embodiment of the present invention with enhanced light reflection on the substrate;

图7为本发明实施例提供的一种第一物理掩膜版的结构示意图;以及FIG. 7 is a schematic structural diagram of a first physical mask provided by an embodiment of the present invention; and

图8为本发明实施例提供的一种第二物理掩膜版的结构示意图。FIG. 8 is a schematic structural diagram of a second physical mask provided by an embodiment of the present invention.

具体实施方式detailed description

下面结合具体实施例对本发明做进一步详细的描述,但本发明的实施方式不限于此。The present invention will be further described in detail below in conjunction with specific examples, but the embodiments of the present invention are not limited thereto.

实施例一Embodiment one

请参见图1及图2,图1为本发明实施例提供的一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的截面示意图;图2为本发明实施例提供的一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的俯视示意图。本发明的N型异质结HEMT包括:蓝宝石衬底1、反光层2、源漏电极3、电子传输层4、光吸收层5、栅电极6。其中,蓝宝石衬底1、反光层2、源漏电极3、电子传输层4、光吸收层5、栅电极6依次形成多层结构。Please refer to Fig. 1 and Fig. 2, Fig. 1 is a schematic cross-sectional view of an N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 materials provided by an embodiment of the present invention with enhanced reflection of substrate; Fig. 2 is an embodiment of the present invention Provided is a schematic top view of an N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 material with enhanced light reflection of the substrate. The N-type heterojunction HEMT of the present invention comprises: a sapphire substrate 1 , a light-reflecting layer 2 , a source-drain electrode 3 , an electron-transporting layer 4 , a light-absorbing layer 5 , and a gate electrode 6 . Among them, the sapphire substrate 1, the reflective layer 2, the source and drain electrodes 3, the electron transport layer 4, the light absorbing layer 5, and the gate electrode 6 form a multilayer structure in sequence.

其中,反光层2可以采用银材料;源漏电极3可以采用金材料;电子传输层4可以采用TiO2材料;所述光吸收层5可以采用CH3NH3PbI3/PCBM材料;所述栅电极6可以采用金材料。Wherein, the reflective layer 2 can be made of silver material; the source and drain electrodes 3 can be made of gold material; the electron transport layer 4 can be made of TiO2 material; the light absorption layer 5 can be made of CH 3 NH 3 PbI 3 /PCBM material; 6 can adopt gold material.

可选地,请参见图3,图3为本发明实施例提供的另一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的截面示意图。该N型异质结HMET还可以包括活性层7,该活性层7可以为PCBM材料。此时,光吸收层可以单纯采用CH3NH3PbI3材料。Optionally, please refer to FIG. 3 . FIG. 3 is a schematic cross-sectional view of another N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 material with enhanced light reflection of the substrate provided by an embodiment of the present invention. The N-type heterojunction HMET may also include an active layer 7, and the active layer 7 may be a PCBM material. In this case, the light absorbing layer may simply use CH 3 NH 3 PbI 3 material.

PCBM材料是一个富勒烯衍生物,分子式是[6,6]-phenyl-C61-butyric acidmethyl ester。由于它的较好的溶解性,很高的电子迁移率,与常见的聚合物给体材料形成良好的相分离,已成为有机太阳能电池的电子受体的标准物。本发明利用了这一特性,将其很巧妙的用于图1或者图3所示的HMET器件中,作为缓冲性质的活性层,能通过对孔洞和空位的填充改善光吸收层薄膜的质量,从而产生更大的晶粒和更少的晶界,吸收更多的光产生光生载流子,增强器件性能。The PCBM material is a fullerene derivative with the molecular formula [6,6]-phenyl-C61-butyric acidmethyl ester. Due to its good solubility, high electron mobility, and good phase separation with common polymer donor materials, it has become the standard electron acceptor for organic solar cells. The present invention utilizes this characteristic, and it is cleverly used in the HMET device shown in Figure 1 or Figure 3, as an active layer with a buffer property, it can improve the quality of the light-absorbing layer film by filling holes and vacancies, As a result, larger grains and fewer grain boundaries are produced, more light is absorbed to generate photogenerated carriers, and device performance is enhanced.

需要说明的是:CH3NH3PbI3材料因在近红外和可见光范围较高的响应度而极适合与在可见光范围的光电探测,其光电灵敏度高,并兼具较高的电子迁移率以及较好的导电性,是制备HEMT的理想材料。It should be noted that the CH 3 NH 3 PbI 3 material is very suitable for photodetection in the visible light range due to its high responsivity in the near-infrared and visible light ranges. It has high photoelectric sensitivity, high electron mobility and Good electrical conductivity is an ideal material for HEMT.

请参见图4,图4为本发明实施例提供的一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的制备方法流程示意图。该方法包括如下步骤:Please refer to FIG. 4 . FIG. 4 is a schematic flowchart of a method for fabricating an N-type heterojunction HEMT based on a CH 3 NH 3 PbI 3 material with enhanced light reflection on a substrate provided by an embodiment of the present invention. The method comprises the steps of:

步骤1、选取蓝宝石衬底;Step 1, select the sapphire substrate;

步骤2、在所述蓝宝石衬底下表面形成反光层;Step 2, forming a reflective layer on the lower surface of the sapphire substrate;

步骤3、在所述蓝宝石衬底上表面制作源漏电极;Step 3, making source and drain electrodes on the upper surface of the sapphire substrate;

步骤4、在所述源漏电极以及未被所述源漏电极覆盖的所述蓝宝石衬底上表面形成电子传输层;Step 4, forming an electron transport layer on the source-drain electrodes and the upper surface of the sapphire substrate not covered by the source-drain electrodes;

步骤5、在所述电子传输层表面形成包括CH3NH3PbI3材料的光吸收层;Step 5, forming a light absorbing layer comprising CH 3 NH 3 PbI 3 on the surface of the electron transport layer;

步骤6、在所述光吸收层表面制作栅电极以最终形成所述N型异质结HEMT。Step 6, making a gate electrode on the surface of the light absorbing layer to finally form the N-type heterojunction HEMT.

其中,步骤2可以包括:Among them, step 2 may include:

以Ag材料作为靶材,以Ar作为溅射气体通入溅射腔,在真空度为6×10-4~1.3×10-3Pa,溅射功率为20~100W的条件下,利用磁控溅射工艺,在所述蓝宝石衬底下表面溅射Ag材料形成所述反光层。Using Ag material as the target material, Ar as the sputtering gas into the sputtering chamber, under the conditions of vacuum degree of 6×10 -4 ~ 1.3×10 -3 Pa, sputtering power of 20 ~ 100W, using magnetron Sputtering process, sputtering Ag material on the lower surface of the sapphire substrate to form the reflective layer.

步骤3可以包括:Step 3 can include:

采用第一物理掩膜版,以Au材料作为靶材,以Ar作为溅射气体通入溅射腔,在真空度为6×10-4~1.3×10-3Pa,溅射功率为20~100W的条件下,在所述蓝宝石衬底上表面溅射Au材料形成所述源漏电极。The first physical mask is used, Au material is used as the target material, Ar is used as the sputtering gas to pass into the sputtering chamber, the vacuum degree is 6×10 -4 ~ 1.3×10 -3 Pa, and the sputtering power is 20~ Under the condition of 100W, Au material is sputtered on the upper surface of the sapphire substrate to form the source and drain electrodes.

步骤4可以包括:Step 4 can include:

以TiO2材料作为靶材,以Ar和O2作为溅射气体通入溅射腔,在真空度为1.3×10-3~3×10-3Pa,溅射功率为60~80W的条件下,在包括所述源漏电极的整个衬底的上表面溅射TiO2材料形成所述源所述电子传输层。Using TiO 2 material as the target material, Ar and O 2 as the sputtering gas into the sputtering chamber, under the conditions of vacuum degree of 1.3×10 -3 ~ 3×10 -3 Pa and sputtering power of 60 ~ 80W , sputtering TiO 2 material on the upper surface of the entire substrate including the source and drain electrodes to form the source and the electron transport layer.

步骤5可以包括:Step 5 can include:

步骤5-11、利用单一旋涂工艺,在所述电子传输层表面旋涂质量浓度为8mg/ml的PCBM材料,退火处理后形成活性层;Step 5-11, using a single spin coating process, spin coating a PCBM material with a mass concentration of 8 mg/ml on the surface of the electron transport layer, and forming an active layer after annealing;

步骤5-12、利用单一旋涂工艺,在所述活性层表面旋涂CH3NH3PbI3材料;Step 5-12, using a single spin-coating process to spin-coat CH 3 NH 3 PbI 3 material on the surface of the active layer;

步骤5-13、利用退火工艺,对所述CH3NH3PbI3材料进行退火处理形成所述光吸收层。Step 5-13, using an annealing process to anneal the CH 3 NH 3 PbI 3 material to form the light absorbing layer.

步骤5还可以包括:Step 5 can also include:

步骤5-21、利用单一旋涂工艺,将CH3NH3PbI3与PCBM的混合溶液旋涂在所述电子传输层表面形成CH3NH3PbI3/PCBM材料;Step 5-21, using a single spin coating process, spin coating a mixed solution of CH 3 NH 3 PbI 3 and PCBM on the surface of the electron transport layer to form a CH 3 NH 3 PbI 3 /PCBM material;

步骤5-22、利用退火工艺,对所述CH3NH3PbI3/PCBM材料进行退火处理形成所述光吸收层。Step 5-22, using an annealing process to anneal the CH 3 NH 3 PbI 3 /PCBM material to form the light absorption layer.

其中,步骤5-21可以包括:Wherein, step 5-21 may include:

步骤5-211、将PbI2材料和CH3NH3I材料先后加入DMSO:GBL溶液中形成PbI2和CH3NH3I的混合溶液;Step 5-211, adding PbI 2 material and CH 3 NH 3 I material to DMSO:GBL solution successively to form a mixed solution of PbI 2 and CH 3 NH 3 I;

步骤5-212、将所述PbI2和CH3NH3I的混合溶液加热搅拌,并进行退火处理后形成CH3NH3PbI3溶液;Step 5-212, heating and stirring the mixed solution of PbI 2 and CH 3 NH 3 I, and performing annealing treatment to form a CH 3 NH 3 PbI 3 solution;

步骤5-213、将所述CH3NH3PbI3溶液和PCBM溶液混合后旋涂子在所述电子传输层表面形成所述CH3NH3PbI3/PCBM材料。Step 5-213, mixing the CH 3 NH 3 PbI 3 solution and the PCBM solution, and then spin-coating to form the CH 3 NH 3 PbI 3 /PCBM material on the surface of the electron transport layer.

步骤6可以包括:Step 6 can include:

采用第二掩膜板,以Au材料作为靶材,以Ar气体作为溅射气体通入溅射腔,在真空度为6×10-4~1.3×10-3Pa,溅射功率为20~100W的条件下,在所述光吸收层表面溅射Au材料形成所述栅电极。Use the second mask plate, use Au material as the target material, and use Ar gas as the sputtering gas to pass into the sputtering chamber. The vacuum degree is 6×10 -4 ~ 1.3×10 -3 Pa, and the sputtering power is 20~ Under the condition of 100W, Au material is sputtered on the surface of the light absorbing layer to form the gate electrode.

需要重点强调的是,反光层的形成并不限定于上述实施例中的执行步骤,其可以在蓝宝石衬底上表面的加工工艺完成后再进行制备,因此,本实施例中关于反光层的制备顺序仅为示例,并以此为限。It should be emphasized that the formation of the reflective layer is not limited to the execution steps in the above-mentioned embodiments, and it can be prepared after the processing technology on the upper surface of the sapphire substrate is completed. Therefore, the preparation of the reflective layer in this embodiment The sequence is an example only and is a limitation.

本实施例,采用由CH3NH3PbI3向沟道提供大量的电子,在衬底下表面镀银形成反射增强型HEMT,具有迁移率高,开关速度快,光吸收以及光利用率增强,光生载流子增多,传输特性增强,光电转换效率大的优点。In this embodiment, CH 3 NH 3 PbI 3 is used to provide a large amount of electrons to the channel, and the lower surface of the substrate is plated with silver to form a reflection-enhanced HEMT, which has high mobility, fast switching speed, enhanced light absorption and light utilization, and light generation. The carrier increases, the transmission characteristics are enhanced, and the photoelectric conversion efficiency is large.

另外,采用在光吸收层加入了PCBM材料形成了异质结,能通过对孔洞和空位的填充改善光吸收层薄膜的质量,从而产生更大的晶粒和更少的晶界,吸收更多的光产生光生载流子,增强器件性能。In addition, the PCBM material is added to the light absorbing layer to form a heterojunction, which can improve the quality of the light absorbing layer film by filling holes and vacancies, resulting in larger grains and fewer grain boundaries, absorbing more The light generates photogenerated carriers and enhances the device performance.

实施例三Embodiment three

请一并参见图5a-图5f及图7和图8,图5a-图5f为本发明实施例提供的一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的制备方法示意图;图7为本发明实施例提供的一种第一物理掩膜版的结构示意图;以及图8为本发明实施例提供的一种第二物理掩膜版的结构示意图。本实施例在上述实施例的基础上,对本发明的基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的制备方法进行详细说明如下:Please refer to Figure 5a-Figure 5f and Figure 7 and Figure 8 together, Figure 5a-Figure 5f is an N-type heterojunction HEMT based on CH 3 NH 3 PbI 3 material provided by an embodiment of the present invention with enhanced light reflection FIG. 7 is a schematic structural diagram of a first physical mask provided by an embodiment of the present invention; and FIG. 8 is a schematic structural diagram of a second physical mask provided by an embodiment of the present invention. In this embodiment, on the basis of the above-mentioned embodiments, the preparation method of the N-type heterojunction HEMT based on the CH 3 NH 3 PbI 3 material of the present invention with enhanced substrate light reflection is described in detail as follows:

步骤1:请参见图5a,准备衬底蓝宝石Al2O3,厚度为200μm~600μm。Step 1: Referring to FIG. 5a, prepare a substrate of sapphire Al 2 O 3 with a thickness of 200 μm-600 μm.

衬底选用蓝宝石Al2O3理由:由于其价格低廉,且绝缘性能好,有效的防止HEMT高电子迁移率晶体管的纵向漏电。The reason for choosing sapphire Al 2 O 3 as the substrate: due to its low price and good insulation performance, it can effectively prevent the vertical leakage of the HEMT high electron mobility transistor.

步骤2:请参见图5b,在蓝宝石衬底背面磁控溅射栅电极银材料形成反光层。Step 2: Please refer to FIG. 5 b , magnetron sputtering the silver material of the grid electrode on the back of the sapphire substrate to form a reflective layer.

采用磁控溅射工艺在步骤1所得衬底背面磁控溅射栅电极银材料,溅射靶材选用质量比纯度>99.99%的银,以质量百分比纯度为99.999%的Ar作为溅射气体通入溅射腔,溅射前,用高纯氩气对磁控溅射设备腔体进行5分钟清洗,然后抽真空。在真空度为6×10-4~1.3×10-3Pa、氩气流量为20-30cm3/秒、靶材基距为10cm和工作功率为20W-100W的条件下,制备反光层银镜,电极厚度为100nm-300nm。The magnetron sputtering process is used to obtain the silver material of the magnetron sputtering grid electrode on the back of the substrate in step 1. The sputtering target material is silver with a mass ratio of purity >99.99%, and Ar with a mass percentage purity of 99.999% is used as the sputtering gas. Before sputtering, clean the cavity of the magnetron sputtering equipment with high-purity argon for 5 minutes, and then vacuumize it. Under the conditions of a vacuum degree of 6×10 -4 ~ 1.3×10 -3 Pa, an argon gas flow rate of 20-30cm3/sec, a target base distance of 10cm and a working power of 20W-100W, a silver mirror with a reflective layer is prepared. The electrode thickness is 100nm-300nm.

反光层可选用Al\Cu等金属替代。The reflective layer can be replaced by metals such as Al\Cu.

步骤3:请参见图5c及图7,使用第一物理掩膜版,在蓝宝石衬底上磁控溅射源漏电极金材料。Step 3: Please refer to FIG. 5 c and FIG. 7 , using the first physical mask to magnetron sputter the gold source and drain electrodes on the sapphire substrate.

溅射靶材选用质量比纯度>99.99%的金,以质量百分比纯度为99.999%的Ar作为溅射气体通入溅射腔,溅射前,用高纯氩气对磁控溅射设备腔体进行5分钟清洗,然后抽真空。在真空度为6×10-4~1.3×10-3Pa、氩气流量为20-30cm3/秒、靶材基距为10cm和工作功率为20W-100W的条件下,制备源漏电极金,电极厚度为100nm~300nm。The sputtering target is made of gold with a mass ratio of purity >99.99%, and Ar with a mass percentage purity of 99.999% is used as the sputtering gas to pass into the sputtering chamber. Rinse for 5 minutes, then vacuum. Under the conditions of vacuum degree of 6×10 -4 ~ 1.3×10 -3 Pa, argon gas flow rate of 20-30cm3/sec, target base distance of 10cm and working power of 20W-100W, the source and drain electrode gold was prepared. The electrode thickness is 100nm-300nm.

源漏电极可选用Al\Ti\Ni\Ag\Pt等金属替代。其中Au\Ag\Pt化学性质稳定;Al\Ti\Ni成本低。The source and drain electrodes can be replaced by metals such as Al\Ti\Ni\Ag\Pt. Among them, Au\Ag\Pt has stable chemical properties; Al\Ti\Ni has low cost.

步骤4:请参见图5d,在步骤3所制备的源漏电极以及未被覆盖的衬底上采用磁控溅射工艺或者原子层沉积工艺淀积电子传输层TiO2材料。Step 4: Referring to FIG. 5d , on the source-drain electrodes prepared in step 3 and the uncovered substrate, magnetron sputtering or atomic layer deposition is used to deposit TiO 2 material for the electron transport layer.

磁控溅射工艺中所用靶材为纯度质量百分比>99.99%的TiO2靶,靶直径为50mm,厚度为1.5-3mm,溅射前,用高纯氩气对磁控溅射设备腔体进行5分钟清洗,然后抽真空,真空度为1.3×10-3~3×10-3Pa,随后依次通入氩气和氧气,通过调节流量控制氩气和氧气的体积比为9:1,总压强保持为2.0Pa,溅射功率为60-80W,生长结束后再经过70℃至150℃的退火处理,由此在源漏电极以及未被覆盖的衬底上制备TiO2电子传输层,传输层厚度为50~200nm。The target used in the magnetron sputtering process is a TiO 2 target with a purity mass percentage >99.99%. The target diameter is 50mm and the thickness is 1.5-3mm. Clean for 5 minutes, then vacuumize, the vacuum degree is 1.3×10 -3 ~ 3×10 -3 Pa, then pass in argon and oxygen in sequence, and control the volume ratio of argon and oxygen to 9:1 by adjusting the flow rate, the total The pressure is kept at 2.0Pa, the sputtering power is 60-80W, and after the growth is completed, it is annealed at 70°C to 150°C to prepare a TiO 2 electron transport layer on the source and drain electrodes and the uncovered substrate. The layer thickness is 50-200 nm.

步骤5:请参见图5e,在电子传输层上材料采用单一旋涂法制备光吸收层。Step 5: Please refer to FIG. 5e, the material on the electron transport layer is prepared by a single spin coating method to prepare a light absorbing layer.

采用单一旋涂法在步骤4所得电子传输层上旋涂CH3NH3PbI3光吸收层,将654mg的PbI2和217mg的CH3NH3I先后加入DMSO:GBL中,得到PbI2和CH3NH3I的混合溶液;将PbI2和CH3NH3I的混合溶液在80摄氏度下搅拌两小时,得到搅拌后的溶液;将搅拌后的溶液在80摄氏度静置1小时,得到CH3NH3PbI3溶液;并按照CH3NH3PbI3:PCBM=100:1的比例溶液滴加到步骤4所得的TiO2薄膜上,在100摄氏度下退火20分钟,形成CH3NH3PbI3/PCBM光吸收层,光吸收层厚度为200~300nm。Spin-coat the CH 3 NH 3 PbI 3 light-absorbing layer on the electron transport layer obtained in step 4 by a single spin coating method, add 654 mg of PbI 2 and 217 mg of CH 3 NH 3 I into DMSO:GBL successively to obtain PbI 2 and CH 3 NH 3 I mixed solution; Stir the mixed solution of PbI 2 and CH 3 NH 3 I at 80 degrees Celsius for two hours to obtain a stirred solution; leave the stirred solution at 80 degrees Celsius for 1 hour to obtain CH 3 NH 3 PbI 3 solution; and according to the ratio of CH 3 NH 3 PbI 3 :PCBM=100:1, the solution is added dropwise on the TiO 2 film obtained in step 4, and annealed at 100 degrees Celsius for 20 minutes to form CH 3 NH 3 PbI 3 /PCBM light absorbing layer, the thickness of the light absorbing layer is 200-300nm.

步骤6:请参见图5f及图8,使用第二物理掩膜版,在光吸收层CH3NH3PbI3/PCBM上磁控溅射栅电极金材料。Step 6: Referring to FIG. 5f and FIG. 8 , use the second physical mask to magnetron sputter the gate electrode gold material on the light absorbing layer CH 3 NH 3 PbI 3 /PCBM.

采用磁控溅射工艺在步骤5所得光吸收层CH3NH3PbI3/PCBM上磁控溅射栅电极金材料,溅射靶材选用质量比纯度>99.99%的金,以质量百分比纯度为99.999%的Ar作为溅射气体通入溅射腔,溅射前,用高纯氩气对磁控溅射设备腔体进行5分钟清洗,然后抽真空。在真空度为6×10-4-1.3×10-3Pa、氩气流量为20~30cm3/秒、靶材基距为10cm和工作功率为20W-100W的条件下,制备栅电极金,电极厚度为100nm~300nm。Using the magnetron sputtering process to magnetron sputter gate electrode gold material on the light absorbing layer CH 3 NH 3 PbI 3 /PCBM obtained in step 5, the sputtering target material is selected from gold with mass ratio purity>99.99%, and the purity in mass percentage is 99.999% Ar is passed into the sputtering chamber as a sputtering gas. Before sputtering, the chamber of the magnetron sputtering equipment is cleaned with high-purity argon for 5 minutes, and then vacuumized. Under the conditions of a vacuum degree of 6×10 -4 -1.3×10 -3 Pa, an argon gas flow rate of 20-30 cm 3 /sec, a target base distance of 10 cm, and a working power of 20W-100W, the gate electrode gold was prepared. The electrode thickness is 100nm-300nm.

实施例四Embodiment four

请参见图6a-图6g,并一并参见图7和图8。图6a-图6g为本发明实施例提供的另一种基于CH3NH3PbI3材料的衬底反光增强的N型异质结HEMT的制备方法示意图。该方法可以包括:Please see Figures 6a-6g, together with Figures 7 and 8. 6a-6g are schematic diagrams of another method for fabricating an N-type heterojunction HEMT based on a CH 3 NH 3 PbI 3 material with enhanced light reflection on a substrate provided by an embodiment of the present invention. The method can include:

步骤1:请参见图6a,准备衬底蓝宝石Al2O3,厚度为200μm~600μm。Step 1: Referring to FIG. 6a, prepare a substrate of sapphire Al 2 O 3 with a thickness of 200 μm-600 μm.

衬底选用蓝宝石Al2O3理由:由于其价格低廉,且绝缘性能好,有效的防止HEMT高电子迁移率晶体管的纵向漏电。The reason for choosing sapphire Al 2 O 3 as the substrate: due to its low price and good insulation performance, it can effectively prevent the vertical leakage of the HEMT high electron mobility transistor.

步骤2:请参见图6b,在蓝宝石衬底背面磁控溅射栅电极银材料形成反光层。Step 2: Please refer to FIG. 6b , magnetron sputtering the silver material of the gate electrode on the back of the sapphire substrate to form a reflective layer.

采用磁控溅射工艺在步骤1所得衬底背面磁控溅射栅电极银材料,溅射靶材选用质量比纯度>99.99%的银,以质量百分比纯度为99.999%的Ar作为溅射气体通入溅射腔,溅射前,用高纯氩气对磁控溅射设备腔体进行5分钟清洗,然后抽真空。在真空度为6×10-4~1.3×10-3Pa、氩气流量为20-30cm3/秒、靶材基距为10cm和工作功率为20W-100W的条件下,制备反光层银镜,电极厚度为100nm-300nm。The magnetron sputtering process is used to obtain the silver material of the magnetron sputtering grid electrode on the back of the substrate in step 1. The sputtering target material is silver with a mass ratio of purity >99.99%, and Ar with a mass percentage purity of 99.999% is used as the sputtering gas. Before sputtering, clean the cavity of the magnetron sputtering equipment with high-purity argon for 5 minutes, and then vacuumize it. Under the conditions of a vacuum degree of 6×10 -4 ~ 1.3×10 -3 Pa, an argon gas flow rate of 20-30cm3/sec, a target base distance of 10cm and a working power of 20W-100W, a silver mirror with a reflective layer is prepared. The electrode thickness is 100nm-300nm.

反光层可选用Al\Cu等金属替代。The reflective layer can be replaced by metals such as Al\Cu.

步骤3:请参见图6c及图7,使用第一物理掩膜版,在蓝宝石衬底上磁控溅射源漏电极金材料。Step 3: Please refer to FIG. 6 c and FIG. 7 , using the first physical mask to magnetron sputter the gold source and drain electrodes on the sapphire substrate.

溅射靶材选用质量比纯度>99.99%的金,以质量百分比纯度为99.999%的Ar作为溅射气体通入溅射腔,溅射前,用高纯氩气对磁控溅射设备腔体进行5分钟清洗,然后抽真空。在真空度为6×10-4~1.3×10-3Pa、氩气流量为20-30cm3/秒、靶材基距为10cm和工作功率为20W-100W的条件下,制备源漏电极金,电极厚度为100nm~300nm。The sputtering target is made of gold with a mass ratio of purity >99.99%, and Ar with a mass percentage purity of 99.999% is used as the sputtering gas to pass into the sputtering chamber. Rinse for 5 minutes, then vacuum. Under the conditions of vacuum degree of 6×10 -4 ~ 1.3×10 -3 Pa, argon gas flow rate of 20-30cm3/sec, target base distance of 10cm and working power of 20W-100W, the source and drain electrode gold was prepared. The electrode thickness is 100nm-300nm.

源漏电极可选用Al\Ti\Ni\Ag\Pt等金属替代。其中Au\Ag\Pt化学性质稳定;Al\Ti\Ni成本低。The source and drain electrodes can be replaced by metals such as Al\Ti\Ni\Ag\Pt. Among them, Au\Ag\Pt has stable chemical properties; Al\Ti\Ni has low cost.

步骤4:请参见图6d,在步骤3所制备的源漏电极以及未被覆盖的衬底上采用磁控溅射工艺或者原子层沉积工艺淀积电子传输层TiO2材料。Step 4: Please refer to FIG. 6d, on the source and drain electrodes prepared in step 3 and the uncovered substrate, magnetron sputtering process or atomic layer deposition process is used to deposit electron transport layer TiO 2 material.

磁控溅射工艺中所用靶材为纯度质量百分比>99.99%的TiO2靶,靶直径为50mm,厚度为1.5-3mm,溅射前,用高纯氩气对磁控溅射设备腔体进行5分钟清洗,然后抽真空,真空度为1.3×10-3~3×10-3Pa,随后依次通入氩气和氧气,通过调节流量控制氩气和氧气的体积比为9:1,总压强保持为2.0Pa,溅射功率为60-80W,生长结束后再经过70℃至150℃的退火处理,由此在源漏电极以及未被覆盖的衬底上制备TiO2电子传输层,传输层厚度为50~200nm。The target used in the magnetron sputtering process is a TiO 2 target with a purity mass percentage >99.99%. The target diameter is 50mm and the thickness is 1.5-3mm. Clean for 5 minutes, then vacuumize, the vacuum degree is 1.3×10 -3 ~ 3×10 -3 Pa, then pass in argon and oxygen in sequence, and control the volume ratio of argon and oxygen to 9:1 by adjusting the flow rate, the total The pressure is kept at 2.0Pa, the sputtering power is 60-80W, and after the growth is completed, it is annealed at 70°C to 150°C to prepare a TiO 2 electron transport layer on the source and drain electrodes and the uncovered substrate. The layer thickness is 50-200 nm.

步骤5:请参见图6e,在电子传输层上材料采用旋涂法制备一薄活性层PCBM。Step 5: Referring to FIG. 6e , a thin active layer PCBM is prepared by spin-coating materials on the electron transport layer.

在电子传输层上采用旋涂活性层,PCBM材料的质量浓度为8mg/ml,优选为16ml。活性层溶液的溶剂选用氯苯,旋涂在充满惰性气体的手套箱中进行,之后在50℃-200℃下退火10分钟-100分钟。活性层的厚度为20nm-100nm。The active layer is spin-coated on the electron transport layer, and the mass concentration of the PCBM material is 8mg/ml, preferably 16ml. The solvent of the active layer solution is chlorobenzene, and the spin coating is carried out in a glove box filled with an inert gas, and then annealed at 50° C.-200° C. for 10 minutes to 100 minutes. The thickness of the active layer is 20nm-100nm.

步骤6:请参见图6f,在活性层上采用单一旋涂法制备光吸收层。Step 6: Referring to FIG. 6f, a light-absorbing layer is prepared on the active layer by a single spin-coating method.

采用单一旋涂法,在步骤5所得活性层上旋涂CH3NH3PbI3光吸收层,将654mg的PbI2和217mg的CH3NH3I先后加入DMSO:GBL中,得到PbI2和CH3NH3I的混合溶液;将PbI2和CH3NH3I的混合溶液在80摄氏度下搅拌两小时,得到搅拌后的溶液;将搅拌后的溶液在80摄氏度静置1小时,得到CH3NH3PbI3溶液;将CH3NH3PbI3溶液滴加到步骤5所得的活性层上,在100摄氏度下退火20分钟,形成CH3NH3PbI3光吸收层,光吸收层厚度为200-300nm。Using a single spin coating method, spin-coat the CH 3 NH 3 PbI 3 light-absorbing layer on the active layer obtained in step 5, add 654 mg of PbI 2 and 217 mg of CH 3 NH 3 I into DMSO:GBL successively to obtain PbI 2 and CH 3 NH 3 I mixed solution; Stir the mixed solution of PbI 2 and CH 3 NH 3 I at 80 degrees Celsius for two hours to obtain a stirred solution; leave the stirred solution at 80 degrees Celsius for 1 hour to obtain CH 3 NH 3 PbI 3 solution; drop CH 3 NH 3 PbI 3 solution onto the active layer obtained in step 5, and anneal at 100 degrees Celsius for 20 minutes to form a CH 3 NH 3 PbI 3 light-absorbing layer with a thickness of 200 -300nm.

步骤7:请参见图6g及图8,使用第二物理掩膜版,在光吸收层上磁控溅射栅电极金材料。Step 7: Referring to FIG. 6g and FIG. 8, use the second physical mask to magnetron sputter gate electrode gold material on the light absorbing layer.

采用磁控溅射工艺在步骤7所得光吸收层上磁控溅射栅电极金材料,溅射靶材选用质量比纯度>99.99%的金,以质量百分比纯度为99.999%的Ar作为溅射气体通入溅射腔,溅射前,用高纯氩气对磁控溅射设备腔体进行5分钟清洗,然后抽真空。在真空度为6×10-4-1.3×10-3Pa、氩气流量为20-30cm3/秒、靶材基距为10cm和工作功率为20W-100W的条件下,制备栅电极金,电极厚度为100nm-300nm。Using the magnetron sputtering process to magnetron sputter gate electrode gold material on the light absorbing layer obtained in step 7, the sputtering target material is selected from gold with a mass ratio purity>99.99%, and Ar with a mass percentage purity of 99.999% is used as the sputtering gas Pass into the sputtering chamber. Before sputtering, clean the chamber of the magnetron sputtering equipment with high-purity argon for 5 minutes, and then vacuumize it. Under the conditions of a vacuum degree of 6×10 -4 -1.3×10 -3 Pa, an argon gas flow rate of 20-30cm 3 /sec, a target base distance of 10cm and a working power of 20W-100W, the gate electrode gold was prepared. The electrode thickness is 100nm-300nm.

以上内容是结合具体的优选实施方式对本发明所作的进一步详细说明,不能认定本发明的具体实施只局限于这些说明。对于本发明所属技术领域的普通技术人员来说,在不脱离本发明构思的前提下,还可以做出若干简单推演或替换,都应当视为属于本发明的保护范围。The above content is a further detailed description of the present invention in conjunction with specific preferred embodiments, and it cannot be assumed that the specific implementation of the present invention is limited to these descriptions. For those of ordinary skill in the technical field of the present invention, without departing from the concept of the present invention, some simple deduction or replacement can be made, which should be regarded as belonging to the protection scope of the present invention.

Claims (9)

1. it is a kind of to be based on CH3NH3PbI3The preparation method of the reflective enhancing N-type hetero-junctions HEMT of substrate of material, it is characterised in that Including:
Choose Sapphire Substrate;
Reflector layer is formed in the Sapphire Substrate lower surface;
Source-drain electrode is made in the Sapphire Substrate upper surface;
The Sapphire Substrate upper surface not covered in the source-drain electrode and by the source-drain electrode forms electric transmission Layer;
Being formed in the electric transmission layer surface includes CH3NH3PbI3The light absorbing zone of material;
Make gate electrode to ultimately form the N-type hetero-junctions HEMT on the light absorbing zone surface.
2. method according to claim 1, it is characterised in that form reflector layer, bag in the Sapphire Substrate lower surface Include:
Using Ag materials as target, sputtering chamber is passed through as sputter gas using Ar, is 6 × 10 in vacuum-4~1.3 × 10-3Pa, Under conditions of sputtering power is 20~100W, using magnetron sputtering technique, Ag materials are sputtered in the Sapphire Substrate lower surface Form the reflector layer.
3. method according to claim 1, it is characterised in that make source-drain electrode in the Sapphire Substrate upper surface, Including:
Using the first physical mask version, using Au materials as target, sputtering chamber is passed through as sputter gas using Ar, is in vacuum 6×10-4~1.3 × 10-3Pa, sputtering power be 20~100W under conditions of, the Sapphire Substrate upper surface sputter Au materials Material forms the source-drain electrode.
4. method according to claim 1, it is characterised in that covered in the source-drain electrode and not by the source-drain electrode The Sapphire Substrate upper surface of lid forms electron transfer layer, including:
With TiO2Material as target, with Ar and O2Sputtering chamber is passed through as sputter gas, is 1.3 × 10 in vacuum-3~3 × 10-3Pa, sputtering power be 60~80W under conditions of, the whole substrate including the source-drain electrode upper surface sputter TiO2 Material forms electron transfer layer described in the source.
5. method according to claim 1, it is characterised in that being formed in the electric transmission layer surface includes CH3NH3PbI3The light absorbing zone of material, including:
It is the PCBM materials of 8mg/ml, annealing in the electric transmission layer surface spin quality concentration using single spin coating proceeding Active layer is formed after treatment;
Using single spin coating proceeding, in the active layer surface spin coating CH3NH3PbI3Material;
Using annealing process, to the CH3NH3PbI3Material carries out annealing and forms the light absorbing zone.
6. method according to claim 1, it is characterised in that being formed in the electric transmission layer surface includes CH3NH3PbI3The light absorbing zone of material, including:
Using single spin coating proceeding, by CH3NH3PbI3The electric transmission layer surface is spin-coated on the mixed solution of PCBM to be formed CH3NH3PbI3/ PCBM materials;
Using annealing process, to the CH3NH3PbI3/ PCBM materials carry out annealing and form the light absorbing zone.
7. method according to claim 6, it is characterised in that by CH3NH3PbI3Institute is spin-coated on the mixed solution of PCBM State electric transmission layer surface and form CH3NH3PbI3/ PCBM materials, including:
By PbI2Material and CH3NH3I materials successively add DMSO:PbI is formed in GBL solution2And CH3NH3The mixed solution of I;
By the PbI2And CH3NH3The mixed solution heating stirring of I, and CH is formed after being made annealing treatment3NH3PbI3Solution;
By the CH3NH3PbI3The electric transmission layer surface is spin-coated on after solution and the mixing of PCBM solution form described CH3NH3PbI3/ PCBM materials.
8. method according to claim 1, it is characterised in that make gate electrode on the light absorbing zone surface, including:
Using the second mask plate, using Au materials as target, sputtering chamber is passed through as sputter gas using Ar gases, is in vacuum 6×10-4~1.3 × 10-3Pa, sputtering power be 20~100W under conditions of, the light absorbing zone surface sputter Au material shapes Into the gate electrode.
9. it is a kind of to be based on CH3NH3PbI3The reflective enhanced N-type hetero-junctions HEMT of substrate of material, it is characterised in that the N-type is different Methods of the matter knot HEMT as described in claim any one of 1-8 is prepared and formed.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018103646A1 (en) * 2016-12-08 2018-06-14 西安电子科技大学 Ch3nh3pbi3 material-based method for fabricating hemt/hhmt device
CN109037387A (en) * 2018-06-11 2018-12-18 烟台工程职业技术学院 One kind being based on CH3NH3PbI3And MoSe2The preparation method of the MOSFET structure light-sensitive device of material
CN109065728A (en) * 2018-08-03 2018-12-21 中国科学院金属研究所 Conducting polymer-lead halide perovskite-conducting polymer sandwich type optoelectronic film preparation method and applications
CN110911565A (en) * 2019-12-04 2020-03-24 西北工业大学 Novel transistor device based on N-type SiC and preparation method thereof
CN111029461A (en) * 2019-12-04 2020-04-17 西北工业大学 Novel transistor device based on P-type SiC and preparation method thereof
CN111029460A (en) * 2019-12-04 2020-04-17 西北工业大学 Novel transistor device based on complementary SiC and preparation method thereof
CN111373563A (en) * 2017-11-20 2020-07-03 乐金显示有限公司 Oxide semiconductor phototransistor with improved visible light absorption and method of making the same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105529403A (en) * 2015-12-08 2016-04-27 电子科技大学 A method for modifying the light-absorbing layer of perovskite solar cells
KR20160095211A (en) * 2015-01-30 2016-08-11 포항공과대학교 산학협력단 Organic-inorganic hybrid perovskite light emitting transister and method of fabricating thereof
CN106129257A (en) * 2016-08-30 2016-11-16 北京大学深圳研究生院 A kind of perovskite thin film phototransistor and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20160095211A (en) * 2015-01-30 2016-08-11 포항공과대학교 산학협력단 Organic-inorganic hybrid perovskite light emitting transister and method of fabricating thereof
CN105529403A (en) * 2015-12-08 2016-04-27 电子科技大学 A method for modifying the light-absorbing layer of perovskite solar cells
CN106129257A (en) * 2016-08-30 2016-11-16 北京大学深圳研究生院 A kind of perovskite thin film phototransistor and preparation method thereof

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018103646A1 (en) * 2016-12-08 2018-06-14 西安电子科技大学 Ch3nh3pbi3 material-based method for fabricating hemt/hhmt device
CN111373563A (en) * 2017-11-20 2020-07-03 乐金显示有限公司 Oxide semiconductor phototransistor with improved visible light absorption and method of making the same
CN111373563B (en) * 2017-11-20 2023-03-31 乐金显示有限公司 Oxide semiconductor phototransistor having improved visible light absorption and method of manufacturing the same
CN109037387A (en) * 2018-06-11 2018-12-18 烟台工程职业技术学院 One kind being based on CH3NH3PbI3And MoSe2The preparation method of the MOSFET structure light-sensitive device of material
CN109065728A (en) * 2018-08-03 2018-12-21 中国科学院金属研究所 Conducting polymer-lead halide perovskite-conducting polymer sandwich type optoelectronic film preparation method and applications
CN110911565A (en) * 2019-12-04 2020-03-24 西北工业大学 Novel transistor device based on N-type SiC and preparation method thereof
CN111029461A (en) * 2019-12-04 2020-04-17 西北工业大学 Novel transistor device based on P-type SiC and preparation method thereof
CN111029460A (en) * 2019-12-04 2020-04-17 西北工业大学 Novel transistor device based on complementary SiC and preparation method thereof

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