[go: up one dir, main page]

CN106567039B - A kind of MoS2/Ag/MoS2Semiconductor film material and preparation method thereof - Google Patents

A kind of MoS2/Ag/MoS2Semiconductor film material and preparation method thereof Download PDF

Info

Publication number
CN106567039B
CN106567039B CN201610902366.7A CN201610902366A CN106567039B CN 106567039 B CN106567039 B CN 106567039B CN 201610902366 A CN201610902366 A CN 201610902366A CN 106567039 B CN106567039 B CN 106567039B
Authority
CN
China
Prior art keywords
mos
thin film
layer
temperature
pressure
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN201610902366.7A
Other languages
Chinese (zh)
Other versions
CN106567039A (en
Inventor
郝兰众
刘云杰
韩治德
薛庆忠
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
China University of Petroleum East China
Original Assignee
China University of Petroleum East China
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by China University of Petroleum East China filed Critical China University of Petroleum East China
Priority to CN201610902366.7A priority Critical patent/CN106567039B/en
Publication of CN106567039A publication Critical patent/CN106567039A/en
Application granted granted Critical
Publication of CN106567039B publication Critical patent/CN106567039B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/34Sputtering
    • C23C14/35Sputtering by application of a magnetic field, e.g. magnetron sputtering
    • C23C14/352Sputtering by application of a magnetic field, e.g. magnetron sputtering using more than one target
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/0623Sulfides, selenides or tellurides
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/14Metallic material, boron or silicon
    • C23C14/18Metallic material, boron or silicon on other inorganic substrates
    • C23C14/185Metallic material, boron or silicon on other inorganic substrates by cathodic sputtering

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Physical Vapour Deposition (AREA)

Abstract

本发明公开一种MoS2/Ag/MoS2半导体薄膜材料及其制备方法,该薄膜为层状结构,由上至下依次包括顶层MoS2薄膜层、Ag金属层、底层MoS2薄膜层和本征绝缘Si基片。其制备方法,主要采用直流磁控溅射技术、利用高能电子依次轰击不同靶材表面:首先使用MoS2靶材,在Si基片表面上沉积上一层底层MoS2薄膜层;然后使用金属Ag靶材,在底层MoS2薄膜层上沉积上一层Ag金属层;最后使用MoS2靶材,在Ag金属层上沉积上一层顶层MoS2薄膜层。相对于纯MoS2薄膜产品,本发明的MoS2/Ag/MoS2半导体薄膜,其电阻率降低了4个数量级以上。本发明的工艺简单、参数控制简便;成品率高、产品质量稳定性与可靠性好,且制造成本低、适于工业化生产。

The invention discloses a MoS 2 /Ag/MoS 2 semiconductor thin film material and a preparation method thereof. The thin film has a layered structure, and comprises a top MoS 2 thin film layer, an Ag metal layer, a bottom MoS 2 thin film layer and the present invention in order from top to bottom. Insulating Si substrate. Its preparation method mainly adopts DC magnetron sputtering technology, and uses high-energy electrons to bombard the surfaces of different targets in turn: first, a MoS 2 target is used, and a bottom layer of MoS 2 film is deposited on the surface of the Si substrate; then metal Ag is used. A target material is used to deposit an Ag metal layer on the bottom MoS 2 thin film layer; finally, a MoS 2 target material is used to deposit a top MoS 2 thin film layer on the Ag metal layer. Compared with the pure MoS 2 thin film product, the resistivity of the MoS 2 /Ag/MoS 2 semiconductor thin film of the present invention is reduced by more than 4 orders of magnitude. The invention has the advantages of simple process, simple parameter control, high yield, good product quality stability and reliability, and low manufacturing cost, which is suitable for industrialized production.

Description

一种MoS2/Ag/MoS2半导体薄膜材料及其制备方法A kind of MoS2/Ag/MoS2 semiconductor thin film material and preparation method thereof

技术领域technical field

本发明涉及一种半导体材料及其制备方法,尤其涉及一种MoS2/Ag/MoS2半导体薄膜材料及其制备方法。The invention relates to a semiconductor material and a preparation method thereof, in particular to a MoS 2 /Ag/MoS 2 semiconductor thin film material and a preparation method thereof.

背景技术Background technique

二硫化钼本身不导电,但具有抗磁性,可用作线性光电导体和显示P型或N型导电性能的半导体,具有整流和换能的作用。Molybdenum disulfide itself is non-conductive, but has diamagnetic properties, and can be used as a linear photoconductor and a semiconductor showing P-type or N-type conductivity, and has the functions of rectification and energy conversion.

由于二硫化钼薄膜材料具有典型的层状结构,层内以共价键紧密结合在一起,每个Mo 原子被六个S原子包围,呈三角棱柱状;层与层之间则以较弱的范德华力相结合,容易滑离。Since the molybdenum disulfide thin film material has a typical layered structure, the layers are tightly bound together by covalent bonds, and each Mo atom is surrounded by six S atoms, in the shape of a triangular prism; Combined with van der Waals forces, it slides off easily.

二硫化钼的上述结构特征导致其电阻率非常大、载流子输运性能较差,使其在半导体及器件领域的应用受到了严重阻碍。The above-mentioned structural characteristics of molybdenum disulfide lead to its very high resistivity and poor carrier transport performance, which seriously hinders its application in the field of semiconductors and devices.

为降低MoS2薄膜材料的电阻率、提高其导电性能,以满足MoS2薄膜材料在半导体器件领域的使用。现有技术中,相对比较成功的做法是,使用金属元素对MoS2进行掺杂,以进行MoS2材料改性。例如:In order to reduce the resistivity of the MoS 2 thin film material and improve its electrical conductivity, so as to satisfy the use of the MoS 2 thin film material in the field of semiconductor devices. In the prior art, a relatively successful approach is to use metal elements to dope MoS 2 to modify the MoS 2 material. E.g:

吴晨等人(《微纳电子技术》,2014,08)公开了“Ag掺杂对MoS2薄膜特性的影响”研究结果,利用化学气相沉积法在p型导电Si基片上制备了Ag掺杂MoS2薄膜材料;Wu Chen et al. ("Micro-Nano Electronics Technology", 2014, 08) disclosed the research results of "Influence of Ag doping on the properties of MoS2 thin films", and prepared Ag-doped on p-type conductive Si substrates by chemical vapor deposition method. MoS 2 thin film material;

中国专利ZL201510558994.3公开了一种Pd-MoS2异质结光伏太阳能电池器件及其制备方法,其采用的技术手段是,使用Pd金属元素进行MoS2掺杂处理。Chinese patent ZL201510558994.3 discloses a Pd-MoS 2 heterojunction photovoltaic solar cell device and a preparation method thereof. The technical means used is to perform MoS 2 doping treatment with Pd metal element.

但是,这种使用金属元素对MoS2进行掺杂,以进行MoS2材料改性的方法,其原理均是,使金属元素进入二硫化钼晶格中,以取代二硫化钼中原来的钼元素。由于原子半径、得失电子能力等方面的差异,这种掺杂技术必然在二硫化钼中形成大量缺陷,从而导致产品的材料结构和性能的不稳定性。However, this method of using metal elements to dope MoS 2 to modify MoS 2 materials is based on the principle that metal elements are introduced into the lattice of molybdenum disulfide to replace the original molybdenum element in molybdenum disulfide. . Due to the differences in atomic radius, ability to gain or lose electrons, etc., this doping technology will inevitably form a large number of defects in molybdenum disulfide, resulting in instability of the material structure and performance of the product.

换言之,采用掺杂的技术手段,以进行MoS2薄膜材料的改性,其产品性能的一致性、稳定性相对较差,产品质量的控制难度大。In other words, using the technical means of doping to modify the MoS 2 thin film material, the consistency and stability of the product performance are relatively poor, and the control of product quality is difficult.

更为重要的是,对于半导体器件技术领域而言,这类掺杂改性后的MoS2薄膜材料,其电阻率仍然偏高、导电性能尚不理想。More importantly, for the technical field of semiconductor devices, such doped and modified MoS 2 thin film materials still have high resistivity and unsatisfactory electrical conductivity.

发明内容SUMMARY OF THE INVENTION

本发明的目的之一是,提供一种具有良好导电性能的MoS2/Ag/MoS2半导体薄膜材料。One of the objectives of the present invention is to provide a MoS 2 /Ag/MoS 2 semiconductor thin film material with good electrical conductivity.

本发明为实现上述目的所需要解决的技术问题是,如何有效降低MoS2薄膜材料的电阻率的技术问题。The technical problem that the present invention needs to solve in order to achieve the above-mentioned purpose is the technical problem of how to effectively reduce the resistivity of the MoS 2 thin film material.

本发明为实现上述目的所采用的技术方案是,一种MoS2/Ag/MoS2半导体薄膜材料,其特征在于,为层状结构,由上至下依次包括顶层MoS2薄膜层、Ag金属层、底层MoS2薄膜层和Si基片;其中:The technical solution adopted by the present invention to achieve the above object is a MoS 2 /Ag/MoS 2 semiconductor thin film material, which is characterized in that it is a layered structure, and sequentially includes a top MoS 2 thin film layer and an Ag metal layer from top to bottom. , the underlying MoS 2 thin film layer and the Si substrate; wherein:

所述Si基片是本征绝缘不导电单晶材料,单面抛光,抛光面为上表面;The Si substrate is an intrinsic insulating non-conductive single crystal material, one side is polished, and the polished surface is the upper surface;

所述MoS2薄膜层,其纯度为99.9%;The MoS 2 thin film layer has a purity of 99.9%;

所述Ag金属层,其纯度为99.99%;The Ag metal layer has a purity of 99.99%;

所述顶层MoS2薄膜层、Ag金属层、底层MoS2薄膜层的厚度分别为50nm、3-10nm和50nm。The thicknesses of the top MoS 2 thin film layer, the Ag metal layer, and the bottom MoS 2 thin film layer are respectively 50 nm, 3-10 nm and 50 nm.

上述技术方案直接带来的技术效果是,在顶层MoS2薄膜层和底层MoS2薄膜层之间插入一层薄Ag金属层,大幅降低了MoS2薄膜材料的电阻率值,显著提高了MoS2薄膜材料的导电性能,并且所形成的MoS2/Ag/MoS2薄膜的结构稳定,性能可重复性强。The technical effect directly brought about by the above technical solutions is that a thin Ag metal layer is inserted between the top MoS 2 thin film layer and the bottom MoS 2 thin film layer, which greatly reduces the resistivity value of the MoS 2 thin film material and significantly improves the MoS 2 The conductive properties of the thin film material, and the formed MoS 2 /Ag/MoS 2 thin film has a stable structure and strong performance repeatability.

检测结果表明,采用上述技术方案所制得的MoS2/Ag/MoS2薄膜材料,电子载流子浓度、电子迁移率分别达到8.3×1022cm-3和8.5cm2V-1s-1The test results show that the MoS 2 /Ag/MoS 2 thin film material prepared by the above technical scheme has an electron carrier concentration and electron mobility of 8.3×10 22 cm -3 and 8.5cm 2 V -1 s -1 , respectively. .

这些性能参数与具有纯MoS2薄膜材料(纯MoS2薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为2.1×1017cm-3、0.1cm2V-1s-1)比较,分别至少提高了5个数量级和1个数量级。These performance parameters are comparable to those of the pure MoS 2 thin film material (the electron carrier concentration, electron mobility and resistivity values of the pure MoS 2 thin film material are 2.1×10 17 cm -3 and 0.1 cm 2 V -1 s -1 , respectively) In comparison, they are improved by at least 5 orders of magnitude and 1 order of magnitude, respectively.

特别是,采用上述技术方案所制得的MoS2/Ag/MoS2薄膜材料,电阻率值达到 5.7×10-2Ωcm,比单一MoS2薄膜材料的电阻率值(1.1×103Ωcm)至少低4个数量级。In particular, the MoS 2 /Ag/MoS 2 thin film material prepared by the above technical solution has a resistivity value of 5.7×10 -2 Ωcm, which is at least 5.7×10 -2 Ωcm than that of a single MoS 2 thin film material (1.1×10 3 Ωcm) 4 orders of magnitude lower.

概括而言,本发明通过将单一的MoS2薄膜层改变为“夹心层”结构形式:采用在上下两层 MoS2薄膜层之间插入一层Ag金属薄层这一简单的技术手段,巧妙地利用所插入的Ag金属薄层中的自由电子对MoS2薄膜层的电子注入效应,提高薄膜材料中的电子载流子浓度和电子迁移率,达到显著降低MoS2薄膜材料的电阻率值、提高MoS2薄膜材料的导电性能的目的。In a nutshell, the present invention subtly changes the single MoS 2 thin film layer into a "sandwich layer" structure by using the simple technical means of inserting a layer of Ag metal thin layer between the upper and lower MoS 2 thin film layers. Using the electron injection effect of the free electrons in the inserted Ag metal thin layer to the MoS 2 thin film layer, the electron carrier concentration and electron mobility in the thin film material are improved, and the resistivity value of the MoS 2 thin film material can be significantly reduced and improved. The purpose of the conductive properties of MoS 2 thin film materials.

为更好地理解上述技术方案,现从原理上进行详细说明:In order to better understand the above technical solutions, the principle is now described in detail:

1、Ag金属插层对MoS2薄膜材料性能达到的技术效果有三个方面:1. The technical effect of Ag metal intercalation on the performance of MoS 2 thin film material has three aspects:

(1)Ag金属插层中的大量自由电子通过注入效应分别进入顶层MoS2薄膜层和底层MoS2薄膜层,分别提高了上下MoS2薄膜层中的电子载流子浓度和电子迁移率;(1) A large number of free electrons in the Ag metal intercalation enter the top MoS 2 thin film layer and the bottom MoS 2 thin film layer respectively through the injection effect, which improves the electron carrier concentration and electron mobility in the upper and lower MoS 2 thin film layers, respectively;

(2)通过提高上下两层MoS2薄膜材料中的电子浓度和电子迁移率,显著降低了MoS2薄膜材料的电阻率,大幅增强了MoS2薄膜材料的导电性能;(2) By increasing the electron concentration and electron mobility in the upper and lower layers of the MoS 2 thin film material, the resistivity of the MoS 2 thin film material is significantly reduced, and the electrical conductivity of the MoS 2 thin film material is greatly enhanced;

(3)中间Ag金属插层的连续性特征,有效增强了薄膜结构的稳定性,减少了薄膜内部缺陷数量,从而使薄膜材料性能的稳定性和可重复性得到提高。(3) The continuity feature of the intermediate Ag metal intercalation effectively enhances the stability of the film structure and reduces the number of internal defects in the film, thereby improving the stability and repeatability of the film material properties.

2、上述技术方案中,Ag金属层的电子功函数为4.2eV,小于MoS2薄膜材料的功函数值4.5eV,从而保证了电子能够由Ag金属层注入进入MoS2薄膜层;2. In the above technical solution, the electronic work function of the Ag metal layer is 4.2eV, which is less than the work function value of the MoS 2 thin film material, which is 4.5 eV, thereby ensuring that electrons can be injected from the Ag metal layer into the MoS 2 thin film layer;

3、上述技术方案中,Ag金属层位于两层MoS2材料之间,利于电子通过注入效应分别进入上下两层MoS2薄膜层,提高整个薄膜材料内部载流子分布的均匀性;3. In the above technical solution, the Ag metal layer is located between the two layers of MoS 2 material, which is beneficial for electrons to enter the upper and lower MoS 2 thin film layers respectively through the injection effect, and improves the uniformity of carrier distribution inside the entire thin film material;

4、上述技术方案中,Ag金属层的厚度超薄,为3-10nm,一方面提高了Ag金属层的均匀连续性;另一方面也避免薄膜内部电子仅以Ag金属层为输运通道,而不经过MoS2薄膜层;同时,Ag金属层可以为上下两层MoS2薄膜提供大量自由电子。4. In the above technical solution, the thickness of the Ag metal layer is ultra-thin, 3-10 nm, which improves the uniformity and continuity of the Ag metal layer on the one hand; Instead of going through the MoS 2 thin film layer; at the same time, the Ag metal layer can provide a lot of free electrons for the upper and lower MoS 2 thin films.

实验证明,上述技术方案的MoS2/Ag/MoS2薄膜材料,具有电子浓度高、电子迁移率大、电阻率值小、结构和性能稳定等优点。Experiments have proved that the MoS 2 /Ag/MoS 2 thin film material of the above technical scheme has the advantages of high electron concentration, high electron mobility, small resistivity value, stable structure and performance, and the like.

优选为,所述底层MoS2薄膜层是采用直流磁控溅射方法沉积于所述Si上表面之上的;Preferably, the underlying MoS 2 thin film layer is deposited on the upper surface of the Si by a DC magnetron sputtering method;

所述Ag金属层是采用直流磁控溅射方法沉积于所述MoS2薄膜层之上的;The Ag metal layer is deposited on the MoS 2 thin film layer by a DC magnetron sputtering method;

所述顶层MoS2薄膜层是采用直流磁控溅射方法沉积于所述Ag金属层之上的。The top MoS 2 thin film layer is deposited on the Ag metal layer by DC magnetron sputtering.

该优选技术方案直接带来的技术效果是,制备方法简单、工艺过程易于控制,产品质量稳定性与一致性更好。The technical effects directly brought about by the preferred technical solution are that the preparation method is simple, the technological process is easy to control, and the product quality stability and consistency are better.

本发明的目的之二是,提供一种上述的MoS2/Ag/MoS2半导体薄膜材料的制备方法,其制备工艺简单、过程易控、成品率高,且工艺环保,适于工业化生产。The second purpose of the present invention is to provide a preparation method of the above-mentioned MoS 2 /Ag/MoS 2 semiconductor thin film material, which has a simple preparation process, an easy-to-control process, a high yield, and an environmentally friendly process, which is suitable for industrial production.

本发明为实现上述目的所采用的技术方案是,一种上述的MoS2/Ag/MoS2薄膜材料的制备方法,其特征在于,包括以下步骤:The technical solution adopted by the present invention to achieve the above object is, a preparation method of the above-mentioned MoS 2 /Ag/MoS 2 thin film material, characterized in that it comprises the following steps:

第一步,硅基片表面清洗步骤The first step, the surface cleaning step of the silicon substrate

选取本征绝缘不导电型Si单晶基片,依次在酒精、丙酮和去离子水中超声清洗180s;Select an intrinsically insulating non-conductive Si single crystal substrate, and ultrasonically clean it in alcohol, acetone and deionized water for 180s in turn;

取出并用干燥氮气吹干;Remove and blow dry with dry nitrogen;

第二步,底层MoS2薄膜层表面沉积步骤The second step, the surface deposition step of the underlying MoS 2 thin film layer

将清洗后的Si单晶基片衬底装入托盘、放入真空腔,并将真空腔抽为高真空,在氩气环境下,将Si单晶基片的温度调至第一温度,氩气气压调至第一压力,采用直流磁控溅射技术,在恒定的30W溅射功率条件下,利用电离出的离子轰击MoS2陶瓷靶材,在所述Si基片的上表面上,沉积一层MoS2薄膜层;Put the cleaned Si single crystal substrate into a tray, put it into a vacuum chamber, and pump the vacuum chamber to a high vacuum. In an argon atmosphere, adjust the temperature of the Si single crystal substrate to the first temperature, and the The gas pressure was adjusted to the first pressure, and the DC magnetron sputtering technology was used to bombard the MoS 2 ceramic target with ionized ions under the condition of constant 30W sputtering power. On the upper surface of the Si substrate, deposition was One MoS 2 thin film layer;

第三步,Ag金属层表面沉积步骤The third step, Ag metal layer surface deposition step

将装有样品的托盘更换至Ag金属靶材的正上方;Change the tray containing the sample to just above the Ag metal target;

将Si单晶基片的温度调至第二温度,Ar气压调至第二压力,采用直流磁控溅射技术,在恒定的30W溅射功率条件下,利用电离出的离子轰击Ag金属靶材,在上述底层MoS2薄膜层的表面上,再沉积一层Ag金属层;The temperature of the Si single crystal substrate was adjusted to the second temperature, and the Ar gas pressure was adjusted to the second pressure. The DC magnetron sputtering technology was used to bombard the Ag metal target with ionized ions under a constant sputtering power of 30W. , on the surface of the above-mentioned bottom MoS 2 thin film layer, a layer of Ag metal layer is deposited;

第四步,顶层MoS2薄膜层表面沉积步骤The fourth step, the surface deposition step of the top MoS 2 thin film layer

将装有样品的托盘再更换至MoS2陶瓷靶材的正上方;Change the tray containing the sample to just above the MoS 2 ceramic target;

将Si单晶基片的温度调至第三温度,Ar气压调至第三压力,采用直流磁控溅射技术,在恒定的30W溅射功率条件下,利用电离出的离子轰击MoS2陶瓷靶材,在上述Ag金属层的表面上,再沉积一层MoS2薄膜层,即得。The temperature of the Si single crystal substrate was adjusted to the third temperature, the Ar gas pressure was adjusted to the third pressure, and the DC magnetron sputtering technology was used to bombard the MoS 2 ceramic target with ionized ions under a constant sputtering power of 30W. A layer of MoS 2 thin film layer is deposited on the surface of the above-mentioned Ag metal layer.

上述技术方案直接带来的技术效果是,制备工艺简单、成品率高,适于工业化生产,并且上述制备方法无有毒有害原料使用、无有毒有害废物产生或废气排放,整个工艺流程绿色环保、无污染;The technical effect directly brought about by the above technical solution is that the preparation process is simple, the yield is high, and it is suitable for industrial production, and the above preparation method does not use toxic and harmful raw materials, does not generate toxic and harmful waste or discharges waste gas, and the entire process flow is green and environmentally friendly. Pollution;

上述技术方案所制得的产品质量均匀稳定、各薄膜层附着牢固、厚度均匀稳定且易于控制。The quality of the product prepared by the above technical solution is uniform and stable, the film layers are firmly attached, the thickness is uniform and stable, and it is easy to control.

优选为,上述氩气的纯度在99.999%以上;所述高纯氮气是指纯度为99.95%以上的干燥氮气;所述MoS2陶瓷靶材,其纯度为99.9%;所述Ag金属靶材,其纯度为99.99%;所述 MoS2靶材的靶基距和所述Ag靶材的靶基距均为50mm。Preferably, the purity of the argon gas is above 99.999%; the high-purity nitrogen gas refers to dry nitrogen gas with a purity of above 99.95%; the MoS 2 ceramic target material has a purity of 99.9%; the Ag metal target material, Its purity is 99.99%; the target-to-base distance of the MoS 2 target material and the target-to-base distance of the Ag target material are both 50 mm.

该优选技术方案直接带来的技术效果是,该距离既能满足离子在运动过程中与工作气体充分碰撞降低动能,又能保证离子在成膜过程中具有足够的附着力。The technical effect directly brought about by the preferred technical solution is that the distance can not only satisfy the sufficient collision of the ions with the working gas to reduce the kinetic energy during the movement, but also ensure that the ions have sufficient adhesion during the film formation process.

进一步优选,上述第一温度为20-400℃,所述第一压力为1-10Pa;Further preferably, the first temperature is 20-400°C, and the first pressure is 1-10Pa;

所述第二温度为20-30℃,所述第二压力为1-5Pa;The second temperature is 20-30°C, and the second pressure is 1-5Pa;

所述第三温度为20-400℃,所述第三压力为1-10Pa。The third temperature is 20-400° C., and the third pressure is 1-10 Pa.

该优选技术方案直接带来的技术效果是,既能保证获得良好的二硫化钼薄膜和银金属膜层的晶体质量,又能满足离子成膜过程中所需的、足够的附着力,同时还能比较容易的控制成膜厚度。The technical effect directly brought about by the preferred technical solution is that it can not only ensure the obtaining of good crystal quality of the molybdenum disulfide thin film and the silver metal film layer, but also meet the sufficient adhesion required in the ion film formation process, and also The film thickness can be easily controlled.

综上所述,本发明相对于现有技术,具有以下有益效果:To sum up, the present invention has the following beneficial effects with respect to the prior art:

1、本发明的MoS2/Ag/MoS2半导体薄膜材料具有十分显著的低电阻率(在室温条件下,电子载流子浓度、电子迁移率和电阻率值分别为8.3×1022cm-3、8.5cm2V-1s-1和5.7×10-2Ωcm。与单一的纯MoS2薄膜材料比较,载流子浓度至少提高了5个数量级,电子迁移率至少提高了1个数量级,而电阻率值至少降低了4个数量级)。1. The MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention has a very significant low resistivity (at room temperature, the electron carrier concentration, electron mobility and resistivity values are 8.3×10 22 cm -3 , 8.5cm 2 V -1 s -1 and 5.7×10 -2 Ωcm. Compared with a single pure MoS 2 thin film material, the carrier concentration is increased by at least 5 orders of magnitude, and the electron mobility is increased by at least 1 order of magnitude, while Resistivity values are reduced by at least 4 orders of magnitude).

2、本发明的MoS2/Ag/MoS2半导体薄膜材料的制备方法具有工艺简单、参数控制简便;且其成品率高、制造成本低、产品质量稳定性与可靠性好,适于工业化生产。2. The preparation method of the MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention has the advantages of simple process, simple parameter control, high yield, low manufacturing cost, good product quality stability and reliability, and is suitable for industrial production.

附图说明Description of drawings

图1为本发明的MoS2/Ag/MoS2半导体薄膜材料的结构示意图;1 is a schematic structural diagram of the MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention;

图2为实施例1所制得的MoS2/Ag/MoS2半导体薄膜材料的拉曼光谱图;Fig. 2 is the Raman spectrum diagram of MoS 2 /Ag/MoS 2 semiconductor thin film material prepared in Example 1;

图3为本发明的MoS2/Ag/MoS2半导体薄膜材料的电子载流子浓度和迁移率值分别随Ag 层厚度变化的变化规律曲线图;3 is a graph showing the variation law of the electron carrier concentration and the mobility value of the MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention with the thickness of the Ag layer, respectively;

图4为本发明的MoS2/Ag/MoS2半导体薄膜材料的电阻率值随Ag层厚度变化的变化规律曲线图。FIG. 4 is a graph showing the variation law of the resistivity value of the MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention with the thickness of the Ag layer.

具体实施方式Detailed ways

下面结合实施例和附图,对本发明进行详细说明。The present invention will be described in detail below with reference to the embodiments and the accompanying drawings.

实施例1Example 1

制备方法如下:The preparation method is as follows:

第一步,硅基片表面清洗步骤The first step, the surface cleaning step of the silicon substrate

选取本征绝缘不导电型Si单晶基片,依次在酒精、丙酮和去离子水中超声清洗180s;Select an intrinsically insulating non-conductive Si single crystal substrate, and ultrasonically clean it in alcohol, acetone and deionized water for 180s in turn;

取出并用干燥氮气吹干;Remove and blow dry with dry nitrogen;

第二步,底层MoS2薄膜层表面沉积步骤The second step, the surface deposition step of the underlying MoS 2 thin film layer

将清洗后的Si单晶基片衬底装入托盘、放入真空腔,并将真空腔抽为高真空,在氩气环境下,将Si单晶基片的温度调至第一温度200℃,氩气气压调至第一压力3Pa,采用直流磁控溅射技术,在恒定的30W溅射功率条件下,利用电离出的离子轰击MoS2陶瓷靶材,在所述Si基片的上表面上,沉积一层厚度为50nm的MoS2薄膜层;Put the cleaned Si single crystal substrate into the tray, put it into a vacuum chamber, and pump the vacuum chamber to a high vacuum, and adjust the temperature of the Si single crystal substrate to the first temperature of 200°C in an argon atmosphere. , the argon gas pressure was adjusted to the first pressure of 3Pa, and the DC magnetron sputtering technology was used. Under the condition of constant 30W sputtering power, the ionized ions were used to bombard the MoS2 ceramic target, and the upper surface of the Si substrate was bombarded by the ionized ions. , deposit a MoS 2 thin film layer with a thickness of 50 nm;

第三步,Ag金属层表面沉积步骤The third step, Ag metal layer surface deposition step

将装有样品的托盘更换至Ag金属靶材的正上方;Change the tray containing the sample to just above the Ag metal target;

将Si单晶基片的温度调至第二温度20-25℃,Ar气压调至第二压力5Pa,采用直流磁控溅射技术,在恒定的30W溅射功率条件下,利用电离出的离子轰击Ag金属靶材,在上述底层MoS2薄膜层的表面上,再沉积一层厚度为10nm的Ag金属层;The temperature of the Si single crystal substrate was adjusted to the second temperature of 20-25°C, the Ar gas pressure was adjusted to the second pressure of 5Pa, and the DC magnetron sputtering technology was used. Under the constant sputtering power of 30W, the ionized ions were used. Bombard the Ag metal target, and deposit another Ag metal layer with a thickness of 10nm on the surface of the above-mentioned bottom MoS 2 thin film layer;

第四步,顶层MoS2薄膜层表面沉积步骤The fourth step, the surface deposition step of the top MoS 2 thin film layer

将装有样品的托盘再更换至MoS2陶瓷靶材的正上方;Change the tray containing the sample to just above the MoS 2 ceramic target;

将Si单晶基片的温度调至第三温度200℃,Ar气压调至第三压力3Pa,采用直流磁控溅射技术,在恒定的30W溅射功率条件下,利用电离出的离子轰击MoS2陶瓷靶材,在上述Ag 金属层的表面上,再沉积一层厚度为50nm的MoS2薄膜层,即得。The temperature of the Si single crystal substrate was adjusted to the third temperature of 200°C, the Ar pressure was adjusted to the third pressure of 3Pa, and the DC magnetron sputtering technology was used to bombard MoS with ionized ions under a constant sputtering power of 30W. 2 The ceramic target is obtained by depositing a MoS 2 thin film layer with a thickness of 50 nm on the surface of the above-mentioned Ag metal layer.

产品性能检测结果:Product performance test results:

经检测,在室温(20-25℃)条件下,所制得的MoS2/Ag/MoS2半导体薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为8.3×1022cm-3、8.5cm2V-1s-1和5.7×10-2Ωcm。After testing, at room temperature (20-25℃), the electron carrier concentration, electron mobility and resistivity of the prepared MoS 2 /Ag/MoS 2 semiconductor thin film material were 8.3×10 22 cm - 3 , 8.5cm 2 V -1 s -1 and 5.7×10 -2 Ωcm.

说明:纯MoS2薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为2.1×1017cm-3、 0.1cm2V-1s-1和1.1×103Ωcm(参见对比实施例:实施例2的检测结果)。Description: The electron carrier concentration, electron mobility and resistivity of pure MoS 2 thin film material are 2.1×10 17 cm -3 , 0.1 cm 2 V -1 s -1 and 1.1×10 3 Ωcm Example: the detection results of Example 2).

实施例2Example 2

说明:该实施例为对比实施例,目标产品为纯MoS2薄膜材料,无中间Ag插层。Note: This example is a comparative example, and the target product is pure MoS 2 thin film material without intermediate Ag intercalation.

制备方法如下:The preparation method is as follows:

第一步,硅基片表面清洗步骤The first step, the surface cleaning step of the silicon substrate

选取本征绝缘不导电型Si单晶基片,依次在酒精、丙酮和去离子水中超声清洗180s;Select an intrinsically insulating non-conductive Si single crystal substrate, and ultrasonically clean it in alcohol, acetone and deionized water for 180s in turn;

取出并用干燥氮气吹干;Remove and blow dry with dry nitrogen;

第二步,底层MoS2薄膜层表面沉积步骤The second step, the surface deposition step of the underlying MoS 2 thin film layer

将清洗后的Si单晶基片衬底装入托盘、放入真空腔,并将真空腔抽为高真空,在氩气环境下,将Si单晶基片的温度调至第一温度200℃,氩气气压调至第一压力3Pa,采用直流磁控溅射技术,在恒定的30W溅射功率条件下,利用电离出的离子轰击MoS2陶瓷靶材,在所述Si基片的上表面上,沉积一层厚度为100nm的MoS2薄膜层;即得。Put the cleaned Si single crystal substrate into the tray, put it into a vacuum chamber, and pump the vacuum chamber to a high vacuum, and adjust the temperature of the Si single crystal substrate to the first temperature of 200°C in an argon atmosphere. , the argon gas pressure was adjusted to the first pressure of 3Pa, and the DC magnetron sputtering technology was used. Under the condition of constant 30W sputtering power, the ionized ions were used to bombard the MoS2 ceramic target, and the upper surface of the Si substrate was bombarded by the ionized ions. , deposit a MoS 2 thin film layer with a thickness of 100 nm;

产品性能检测结果:Product performance test results:

经检测,在室温(20-25℃)条件下,所制得的MoS2薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为2.1×1017cm-3、0.1cm2V-1s-1和1.1×103Ωcm。After testing, at room temperature (20-25℃), the electron carrier concentration, electron mobility and resistivity of the prepared MoS 2 thin film material are 2.1×10 17 cm -3 and 0.1 cm 2 V, respectively. -1 s -1 and 1.1×10 3 Ωcm.

实施例3Example 3

仅在第三步中,通过调整溅射时间,将Ag中间插层厚度调整为3nm;其余,均同实施例1。Only in the third step, the thickness of the Ag intercalation layer was adjusted to 3 nm by adjusting the sputtering time;

产品性能检测结果:Product performance test results:

经检测,在室温(20-25℃)条件下,所制得的MoS2/Ag/MoS2薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为1.8×1020cm-3、1.2cm2V-1s-1和9.8Ωcm。After testing, at room temperature (20-25℃), the electron carrier concentration, electron mobility and resistivity of the prepared MoS 2 /Ag/MoS 2 thin film material were 1.8×10 20 cm -3 , 1.2cm 2 V -1 s -1 and 9.8Ωcm.

实施例4Example 4

仅在第三步中,通过调整溅射时间,将Ag中间插层厚度调整为8nm;其余,均同实施例1。Only in the third step, the thickness of the Ag intermediate intercalation layer was adjusted to 8 nm by adjusting the sputtering time; the rest were the same as in Example 1.

产品性能检测结果:Product performance test results:

经检测,在室温(20-25℃)条件下,所制得的MoS2/Ag/MoS2半导体薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为8.8×1021cm-3、2.3cm2V-1s-1和1.1Ωcm。After testing, at room temperature (20-25℃), the electron carrier concentration, electron mobility and resistivity of the prepared MoS 2 /Ag/MoS 2 semiconductor thin film material are 8.8×10 21 cm - 3 , 2.3cm 2 V -1 s -1 and 1.1Ωcm.

实施例5Example 5

仅在第三步中,通过调整溅射时间,将Ag中间插层厚度调整为10nm;其余,均同实施例1。Only in the third step, the thickness of the Ag intermediate intercalation layer was adjusted to 10 nm by adjusting the sputtering time; the rest were the same as in Example 1.

产品性能检测结果:Product performance test results:

经检测,在室温(20-25℃)条件下,所制得的MoS2/Ag/MoS2半导体薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为6.0×1022cm-3、5.7cm2V-1s-1和0.12Ωcm。After testing, at room temperature (20-25℃), the electron carrier concentration, electron mobility and resistivity of the prepared MoS 2 /Ag/MoS 2 semiconductor thin film material were 6.0×10 22 cm - 3 , 5.7cm 2 V -1 s -1 and 0.12Ωcm.

为更好地理解本发明的技术特点,下面结合附图,对本发明所制得的产品的性能检测方法和检测结果进行详细说明。In order to better understand the technical characteristics of the present invention, the performance testing method and testing result of the product prepared by the present invention will be described in detail below with reference to the accompanying drawings.

图1为本发明的MoS2/Ag/MoS2半导体薄膜材料的结构示意图。FIG. 1 is a schematic structural diagram of the MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention.

如图1所示,本发明的MoS2/Ag/MoS2半导体薄膜材料,其为层状结构,由上至下依次包括顶层MoS2薄膜层、Ag金属层、底层MoS2薄膜层和Si基片;其中:As shown in FIG. 1 , the MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention has a layered structure, and from top to bottom sequentially includes a top MoS 2 thin film layer, an Ag metal layer, a bottom MoS 2 thin film layer and a Si base layer. piece; of which:

上述Si基片是本征绝缘不导电单晶材料,单面抛光,抛光面为上表面;The above-mentioned Si substrate is an intrinsically insulating non-conductive single crystal material, one side is polished, and the polished surface is the upper surface;

上述MoS2薄膜层,其纯度为99.9%;The above MoS 2 thin film layer, its purity is 99.9%;

上述Ag金属层,其纯度为99.99%;The above-mentioned Ag metal layer has a purity of 99.99%;

上述顶层MoS2薄膜层、Ag金属层、底层MoS2薄膜层的厚度分别为50nm、3-10nm和50nm;The thicknesses of the top MoS 2 thin film layer, the Ag metal layer and the bottom MoS 2 thin film layer are respectively 50nm, 3-10nm and 50nm;

上述底层MoS2薄膜层是采用直流磁控溅射方法沉积于上述Si上表面之上的;The above-mentioned bottom layer MoS 2 thin film layer is deposited on the above-mentioned Si upper surface by DC magnetron sputtering method;

上述Ag金属层是采用直流磁控溅射方法沉积于上述MoS2薄膜层之上的;The above-mentioned Ag metal layer is deposited on the above-mentioned MoS 2 thin film layer by DC magnetron sputtering method;

上述顶层MoS2薄膜层是采用直流磁控溅射方法沉积于上述Ag金属层之上的。The above-mentioned top MoS 2 thin film layer is deposited on the above-mentioned Ag metal layer by DC magnetron sputtering method.

图2为实施例1所制得的MoS2/Ag/MoS2半导体薄膜材料的拉曼光谱分析图。FIG. 2 is a Raman spectrum analysis diagram of the MoS 2 /Ag/MoS 2 semiconductor thin film material prepared in Example 1. FIG.

如图2所示,382cm-1和407cm-1分别为MoS2薄膜的典型面内振动模式(E1 2g)和面外振动模式(A1g)。表明所制得的薄膜材质为MoS2As shown in Fig. 2, 382 cm -1 and 407 cm -1 are the typical in-plane vibration modes (E 1 2g ) and out-of-plane vibration modes (A 1g ) of MoS 2 thin films, respectively. It is indicated that the material of the prepared film is MoS 2 .

图3为本发明的MoS2/Ag/MoS2半导体薄膜材料的电子载流子浓度和迁移率值随Ag层厚度变化的变化规律曲线图。FIG. 3 is a graph showing the changing law of the electron carrier concentration and mobility value of the MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention as a function of the thickness of the Ag layer.

从图3中可以看出,随着Ag中间插层厚度的增加,MoS2/Ag/MoS2薄膜材料的电子载流子浓度和迁移率值逐渐增大。可见,随着厚度的增加,Ag中间插层的均匀连续性增强,是Ag层内部向MoS2薄膜中注入的电子数目和效果增强,从而导致整个薄膜的载流子浓度和电子迁移率发生明显提高。It can be seen from Figure 3 that the electron carrier concentration and mobility values of the MoS 2 /Ag/MoS 2 thin film material gradually increase with the increase of the Ag intercalation thickness. It can be seen that with the increase of thickness, the uniformity and continuity of the Ag intercalation layer is enhanced, which is due to the enhancement of the number and effect of electrons injected into the MoS2 film from the inside of the Ag layer, which leads to the obvious occurrence of carrier concentration and electron mobility in the whole film. improve.

图4为本发明的MoS2/Ag/MoS2半导体薄膜材料的电阻率值随Ag层厚度变化的变化规律曲线图。FIG. 4 is a graph showing the variation law of the resistivity value of the MoS 2 /Ag/MoS 2 semiconductor thin film material of the present invention with the thickness of the Ag layer.

如图4所示,无Ag金属插层(对应于图中的厚度为0时)的纯MoS2薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为2.1×1017cm-3、0.1cm2V-1s-1和1.1×103Ωcm。As shown in Fig. 4 , the electron carrier concentration, electron mobility and resistivity values of pure MoS2 thin film material without Ag metal intercalation (corresponding to the thickness of 0 in the figure) are 2.1 × 10 17 cm − 3 , 0.1 cm 2 V -1 s -1 and 1.1×10 3 Ωcm.

从图4中可以看出,随着Ag中间插层厚度的增加,MoS2/Ag/MoS2薄膜材料的电阻率值逐渐减小。It can be seen from Figure 4 that the resistivity value of the MoS 2 /Ag/MoS 2 thin film material gradually decreases with the increase of the Ag intercalation thickness.

在室温(20-25℃)条件下,所制得的具有10nm Ag金属插层的MoS2/Ag/MoS2半导体薄膜材料的电子载流子浓度、电子迁移率和电阻率值分别为8.3×1022cm-3、8.5cm2V-1s-1和5.7×10-2Ωcm。At room temperature (20-25°C), the electron carrier concentration, electron mobility and resistivity of the prepared MoS 2 /Ag/MoS 2 semiconductor thin film material with 10 nm Ag metal intercalation were 8.3× 10 22 cm -3 , 8.5 cm 2 V -1 s -1 and 5.7×10 -2 Ωcm.

数据对比可以看出,载流子浓度提高幅度超过5个数量级,电子迁移率提高幅度超过1 个数量级,而电阻率值降低幅度超过4个数量级,导电性能改善幅度巨大、效果十分显著。From the data comparison, it can be seen that the increase of the carrier concentration is more than 5 orders of magnitude, the increase of the electron mobility is more than 1 order of magnitude, and the decrease of the resistivity value is more than 4 orders of magnitude. The improvement of the electrical conductivity is huge and the effect is very significant.

Claims (1)

1. a kind of MoS2/Ag/MoS2The preparation method of semiconductor film material, which comprises the following steps:
The first step, silicon substrate surface cleaning step
The intrinsic non-conductive type Si monocrystal chip of insulation is chosen, is successively cleaned by ultrasonic 180s in alcohol, acetone and deionized water;
It takes out and is dried up with drying nitrogen;
Second step, bottom MoS2Thin-film surface deposition step
Si monocrystal chip substrate after cleaning is packed into pallet, is put into vacuum chamber, and vacuum chamber is taken out as high vacuum, in argon gas ring Under border, the temperature of Si monocrystal chip is adjusted to the first temperature, ar pressure is adjusted to first pressure, using magnetically controlled DC sputtering skill Art utilizes the ion bombardment MoS ionized out under the conditions of constant 30W sputtering power2Ceramic target, in the Si substrate On upper surface, one layer of MoS is deposited2Film layer;
Third step, Ag layer on surface of metal deposition step
By the pallet-changing equipped with sample to the surface of Ag metal targets;
The temperature of Si monocrystal chip is adjusted to second temperature, Ar air pressure is adjusted to second pressure, using magnetically controlled DC sputtering technology, Under the conditions of constant 30W sputtering power, using the ion bombardment Ag metal targets ionized out, in above-mentioned bottom MoS2Film layer On surface, redeposited one layer of Ag metal layer;
4th step, top layer MoS2Thin-film surface deposition step
Pallet equipped with sample is replaced again to MoS2The surface of ceramic target;
The temperature of Si monocrystal chip is adjusted to third temperature, Ar air pressure is adjusted to third pressure, using magnetically controlled DC sputtering technology, Under the conditions of constant 30W sputtering power, the ion bombardment MoS ionized out is utilized2Ceramic target, on the surface of above-mentioned Ag metal layer On, one layer of MoS of redeposition2Film layer to get;
In above-mentioned steps, the purity of the argon gas is 99.999% or more;
The nitrogen refers to that purity is 99.95% or more drying nitrogen;
The MoS2Ceramic target, purity 99.9%;
The Ag metal targets, purity 99.99%;
The MoS2The target-substrate distance of the target-substrate distance of target and the Ag target is 50mm;
First temperature is 20-400 DEG C, and the first pressure is 1-10Pa;
The second temperature is 20-30 DEG C, and the second pressure is 1-5Pa;
The third temperature is 20-400 DEG C, and the third pressure is 1-10Pa.
CN201610902366.7A 2016-10-17 2016-10-17 A kind of MoS2/Ag/MoS2Semiconductor film material and preparation method thereof Expired - Fee Related CN106567039B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610902366.7A CN106567039B (en) 2016-10-17 2016-10-17 A kind of MoS2/Ag/MoS2Semiconductor film material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610902366.7A CN106567039B (en) 2016-10-17 2016-10-17 A kind of MoS2/Ag/MoS2Semiconductor film material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN106567039A CN106567039A (en) 2017-04-19
CN106567039B true CN106567039B (en) 2019-06-25

Family

ID=58532037

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610902366.7A Expired - Fee Related CN106567039B (en) 2016-10-17 2016-10-17 A kind of MoS2/Ag/MoS2Semiconductor film material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN106567039B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108176393A (en) * 2017-12-27 2018-06-19 肇庆市华师大光电产业研究院 A kind of orderly, high density Ag-Al2O3-MoS2The preparation method of nanostructured
CN111455318A (en) * 2020-06-01 2020-07-28 中国科学院兰州化学物理研究所 A kind of molybdenum nitride/molybdenum disulfide/silver ternary composite high temperature solid lubricating film and preparation method thereof
CN112359318A (en) * 2020-10-19 2021-02-12 西安交通大学 MoS containing 1T phase2Film and preparation process thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7141489B2 (en) * 2003-05-20 2006-11-28 Burgener Ii Robert H Fabrication of p-type group II-VI semiconductors
CN101834231A (en) * 2009-02-06 2010-09-15 齐伦投资专利Ii两合公司 Method for manufacturing thin film photovoltaic system and thin film photovoltaic system
CN104979037A (en) * 2015-05-14 2015-10-14 上海电力学院 Transparent conducting thin film with enhanced thermal stability and preparation method and application thereof
CN106024978A (en) * 2016-06-16 2016-10-12 华东师范大学 Transparent conductive thin film with metal alloy sandwich structure with anti-ultraviolet function

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7141489B2 (en) * 2003-05-20 2006-11-28 Burgener Ii Robert H Fabrication of p-type group II-VI semiconductors
CN101834231A (en) * 2009-02-06 2010-09-15 齐伦投资专利Ii两合公司 Method for manufacturing thin film photovoltaic system and thin film photovoltaic system
CN104979037A (en) * 2015-05-14 2015-10-14 上海电力学院 Transparent conducting thin film with enhanced thermal stability and preparation method and application thereof
CN106024978A (en) * 2016-06-16 2016-10-12 华东师范大学 Transparent conductive thin film with metal alloy sandwich structure with anti-ultraviolet function

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"纳米Ag夹层ZnO薄膜的光电性能";闫金良等;《纳米技术与精密工程》;20100115;第8卷(第1期);第12-15页
"银掺杂对MoS2薄膜特性的影响";吴晨等;《材料与结构》;20140815(第8期);第498-502页

Also Published As

Publication number Publication date
CN106567039A (en) 2017-04-19

Similar Documents

Publication Publication Date Title
CN101517122B (en) Method for depositing an oxide layer on absorbers of solar cells, solar cell and use of the method
CN104617165B (en) A kind of molybdenum disulfide/buffer layer/silicon n-i-p solar cell device and preparation method thereof
Zhao et al. Stoichiometry control of sputtered zinc oxide films by adjusting Ar/O2 gas ratios as electron transport layers for efficient planar perovskite solar cells
CN106567039B (en) A kind of MoS2/Ag/MoS2Semiconductor film material and preparation method thereof
JPWO2010084758A1 (en) Solar cell manufacturing method and solar cell
Zhu et al. Aluminium doped zinc oxide sputtered from rotatable dual magnetrons for thin film silicon solar cells
CN107742661A (en) Method for preparing inorganic tin-based perovskite solar cells by physical vapor deposition
CN106816494A (en) A kind of method of heterojunction solar battery reduction series resistance
CN114242897A (en) A kind of encapsulation method of perovskite optoelectronic device
CN102569481B (en) Nano silicon window layer with gradient band gap characteristic and preparation method thereof
CN110416413B (en) A kind of perovskite solar cell with high-performance gradient electron transport layer and its preparation method
CN106449795A (en) A kind of MoS2/Si photovoltaic device with ITO/Pd double-layer structure composite electrode and preparation method thereof
CN102277570A (en) Method for preparing ZnO/Cu/ZnO transparent conductive thin film
CN109616533B (en) Crystalline silicon heterojunction solar cell and preparation method thereof
CN108010973A (en) A kind of preparation method of low-defect-density amorphous oxide molybdenum hole transmission layer
CN111341861A (en) Photovoltaic infrared detector based on p-GeTe/n-Si and preparation method thereof
CN106505046B (en) It is a kind of using insulating substrate as carbon-aluminium-carbon semiconductor film material of substrate and preparation method thereof
CN213708464U (en) Magnetron Sputtering Coater
CN101660132B (en) A kind of method for preparing hydrogenated silicon carbon film by magnetron sputtering
JP4804505B2 (en) Sputtering apparatus and film forming method
CN102751381A (en) Preparation method for copper indium selenium base film solar cell molybdenum electrode
TW200937661A (en) Solar cell manufacturing method
CN101692751B (en) Device structure for realizing ZnO film pure ultraviolet electroluminescence on p-type silicon
CN105200382B (en) A kind of Ge adulterates Mg2Si base thermal electric films and preparation method thereof
CN105405684B (en) A kind of method that plasma treatment improves Al colelctor electrodes

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20190625

CF01 Termination of patent right due to non-payment of annual fee