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CN101488555A - Manufacturing method for low power consumption phase changing memory - Google Patents

Manufacturing method for low power consumption phase changing memory Download PDF

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CN101488555A
CN101488555A CNA200910046056XA CN200910046056A CN101488555A CN 101488555 A CN101488555 A CN 101488555A CN A200910046056X A CNA200910046056X A CN A200910046056XA CN 200910046056 A CN200910046056 A CN 200910046056A CN 101488555 A CN101488555 A CN 101488555A
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preparation
bottom electrode
power consumption
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吕士龙
宋志棠
刘波
封松林
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Shanghai Institute of Microsystem and Information Technology of CAS
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Abstract

本发明涉及利用FIB沉积纳米锥形底电极从而制备硫系化合物存储单元器件的方法,其包括以下步骤:首先,在(100)取向的硅片上面,应用化学气相沉积的方法制备一层SixN介质层;然后使用磁控溅射的方法沉积Al/Ti/TiN作为底层电极材料;于底层电极材料上利用离子束法沉积氧化硅作为介质层;利用电子束曝光结合反应离子刻蚀的方法制备若干氧化硅孔;于氧化硅孔内利用聚焦离子束系统制备所需要的锥形底电极;利用光刻剥离的方法于底电极上沉积相变材料层;之后利用聚焦离子束引出上层测试电极;最后离子束沉积法溅射氧化硅作为绝热保护层。本发明有助于制备新型的低功耗相变存储器,为研究20nm以下尺寸相变存储器的性能提供有效的方法,促进相变存储器的发展。

Figure 200910046056

The invention relates to a method for preparing a chalcogenide compound storage unit device by depositing a nano-conical bottom electrode using FIB, which includes the following steps: first, on a (100)-oriented silicon wafer, a layer of Si x is prepared by chemical vapor deposition N dielectric layer; then use magnetron sputtering to deposit Al/Ti/TiN as the bottom electrode material; use ion beam method to deposit silicon oxide as the dielectric layer on the bottom electrode material; use electron beam exposure combined with reactive ion etching method Prepare a number of silicon oxide holes; use the focused ion beam system to prepare the required conical bottom electrode in the silicon oxide hole; use the photolithographic stripping method to deposit a phase change material layer on the bottom electrode; then use the focused ion beam to extract the upper test electrode ; Finally, ion beam deposition sputtered silicon oxide as a heat insulating protective layer. The invention helps to prepare a novel low-power phase-change memory, provides an effective method for studying the performance of the phase-change memory with a size below 20nm, and promotes the development of the phase-change memory.

Figure 200910046056

Description

一种低功耗相变存储器的制备方法 A kind of preparation method of low power consumption phase change memory

技术领域 technical field

本发明涉及一种含新电极结构的相变存储器的制备方法,属于微电子领域。The invention relates to a preparation method of a phase-change memory with a new electrode structure, which belongs to the field of microelectronics.

背景技术 Background technique

硫系化合物随机存储器是基于S.R.Ovshinsky在20世纪60年代末70年代初提出的硫系化合物薄膜可以应用于相变存储介质的构想基础上发展而来的。2001年intel公司首次报道4MB的C-RAM,2006年底Samsung公司已经报道了512MB C-RAM。目前主流的非挥发性存储器主要是闪存。但是按照摩尔定律,现有的存储单元设计在45nm制程以下时,很难继续保持其非易失性的特性。相变存储器由于在写入新数据时无须进行擦去原数据的处理,其数据写入速度可达到传统闪存的几十至几百倍,而功耗却不到闪存的一半,尺寸也比闪存小很多;并且相变存储器的耐用性极佳,使用寿命远长于传统闪存。基于这些因素,业界普遍认为在45nm以下,相变存储器将会代替flash成为主流的非挥发性存储器。目前国际上有Ovonyx、Intel、Samsung、STMicroelectronics、Infineon、Elpida、Philips和IBM等公司在开展相变存储器的研究,其方向向着高速、高密度、低功耗的方面发展。他们关注的焦点都集中在如何尽快实现相变存储器的商业化上,其中器件的功耗降低是非常关键和重要的,因为相变存储器器件单元的相变过程最终要靠金属互补氧化物半导体管的驱动来实现,为了实现与高密度存储芯片中的CMOS管功率相匹配,必需降低器件的功耗。降低器件功耗的方法有:减小电极与相变材料的接触面积;提高相变材料的电阻;在电极与相变材料之间或相变材料内部添加热阻层等等。减小电极与相变材料的接触面积可以有效的降低相变材料的体积,从而降低功耗,这正是本发明的出发点。Chalcogenide random access memory is developed based on the idea that chalcogenide thin films can be applied to phase-change storage media proposed by S.R. Ovshinsky in the late 1960s and early 1970s. In 2001, Intel first reported 4MB of C-RAM, and by the end of 2006, Samsung had reported 512MB of C-RAM. At present, the mainstream non-volatile memory is mainly flash memory. However, according to Moore's law, when the existing memory cell design is below 45nm, it is difficult to maintain its non-volatile characteristics. Since phase change memory does not need to erase the original data when writing new data, its data writing speed can reach tens to hundreds of times that of traditional flash memory, while its power consumption is less than half of that of flash memory, and its size is also smaller than that of flash memory. Much smaller; and the durability of phase change memory is excellent, and the service life is much longer than that of traditional flash memory. Based on these factors, the industry generally believes that below 45nm, phase-change memory will replace flash as the mainstream non-volatile memory. At present, companies such as Ovonyx, Intel, Samsung, STMicroelectronics, Infineon, Elpida, Philips, and IBM are conducting research on phase change memory in the world, and their direction is developing towards high speed, high density, and low power consumption. The focus of their attention is on how to realize the commercialization of phase change memory as soon as possible, in which the reduction of power consumption of the device is very critical and important, because the phase change process of the phase change memory device unit ultimately depends on metal complementary oxide semiconductor transistors. In order to achieve the power matching with the CMOS tube in the high-density memory chip, it is necessary to reduce the power consumption of the device. The methods to reduce the power consumption of the device include: reducing the contact area between the electrode and the phase change material; increasing the resistance of the phase change material; adding a thermal resistance layer between the electrode and the phase change material or inside the phase change material, etc. Reducing the contact area between the electrodes and the phase-change material can effectively reduce the volume of the phase-change material, thereby reducing power consumption, which is the starting point of the present invention.

发明内容 Contents of the invention

本发明要解决的技术问题在于提供一种低功耗相变存储器的制备方法,减小电极与相变材料的接触面积可以有效的降低相变材料的体积,从而降低功耗。The technical problem to be solved by the present invention is to provide a method for preparing a low-power phase-change memory. Reducing the contact area between the electrodes and the phase-change material can effectively reduce the volume of the phase-change material, thereby reducing power consumption.

为了解决上述技术问题,本发明采用如下技术方案:一种低功耗相变存储器的制备方法,该方法主要包括以下步骤:In order to solve the above-mentioned technical problems, the present invention adopts the following technical scheme: a method for preparing a low-power phase-change memory, which mainly includes the following steps:

1)在硅片衬底上制备一层SixN介质层;1) preparing a layer of Six N dielectric layer on the silicon wafer substrate;

2)在SixN介质层上制备底层电极材料层;2) preparing a bottom electrode material layer on the Six N dielectric layer;

3)在底层电极材料层上制备氧化硅介质层;3) preparing a silicon oxide dielectric layer on the bottom electrode material layer;

4)在氧化硅介质层上制备氧化硅孔;4) preparing silicon oxide holes on the silicon oxide dielectric layer;

5)在氧化硅孔内利用聚焦离子束沉积金属制备锥形底电极;5) Using focused ion beam to deposit metal in silicon oxide pores to prepare conical bottom electrodes;

6)在锥形底电极上沉积相变材料层;6) Depositing a phase change material layer on the conical bottom electrode;

7)在相变材料层上引出上层测试电极。7) Lead out the upper test electrode on the phase change material layer.

作为本发明的优选方案之一,步骤5)中在氧化硅孔内利用聚焦离子束沉积金属制备锥形底电极,该金属包括铂、钨、钛、金、氮化钛、钨钛中的一种或几种。As one of the preferred solutions of the present invention, in step 5) in the silicon oxide hole, a conical bottom electrode is prepared by using focused ion beam deposition metal, and the metal includes one of platinum, tungsten, titanium, gold, titanium nitride, and tungsten titanium. species or several.

作为本发明的优选方案之一,所述SixN介质层,其厚度为300~500nm。As one of the preferred solutions of the present invention, the thickness of the Six N dielectric layer is 300-500 nm.

作为本发明的优选方案之一,所述底层电极材料层是用磁控溅射的方法形成的底层电极Al/Ti/TiN,其相应的厚度为150nm/100nm/50nm。As one of the preferred solutions of the present invention, the bottom electrode material layer is the bottom electrode Al/Ti/TiN formed by magnetron sputtering, and its corresponding thickness is 150nm/100nm/50nm.

作为本发明的优选方案之一,所述氧化硅孔的制备利用电子束曝光结合反应离子刻蚀完成,氧化硅孔的直径为40~60nm,孔的深度大于氧化硅介质层的厚度。。As one of the preferred solutions of the present invention, the preparation of the silicon oxide holes is completed by electron beam exposure combined with reactive ion etching, the diameter of the silicon oxide holes is 40-60 nm, and the depth of the holes is greater than the thickness of the silicon oxide dielectric layer. .

作为本发明的优选方案之一,所述锥形底电极底部直径为40~60nm,锥形底电极高度高于氧化硅孔的高度。As one of the preferred solutions of the present invention, the diameter of the bottom of the conical bottom electrode is 40-60 nm, and the height of the conical bottom electrode is higher than the height of the silicon oxide pores.

作为本发明的优选方案之一,所述相变材料的沉积利用磁控溅射结合剥离完成,即磁控溅射沉积相变材料后采用丙酮浸泡将光刻胶及其上面沉积的相变材料去除。As one of the preferred solutions of the present invention, the deposition of the phase change material is completed by magnetron sputtering combined with stripping, that is, after the phase change material is deposited by magnetron sputtering, the photoresist and the phase change material deposited on it are soaked in acetone remove.

作为本发明的优选方案之一,所述上层测试电极利用聚焦离子束沉积铂引出,引出电极的线宽控制为100nm以下,电极厚度为80nm。As one of the preferred solutions of the present invention, the upper test electrode is extracted by focused ion beam deposition of platinum, the line width of the extraction electrode is controlled to be below 100nm, and the electrode thickness is 80nm.

作为本发明的优选方案之一,该方法进一步包括在上层测试电极上利用离子束沉积法沉积氧化硅制备顶层绝热保护层,氧化硅的厚度为200nm。As one of the preferred solutions of the present invention, the method further includes depositing silicon oxide on the upper test electrode by means of ion beam deposition to prepare a top thermal insulation protection layer, and the thickness of the silicon oxide is 200nm.

作为本发明的优选方案之一,在制备SixN介质层之前先清洗硅片,具体步骤如下:采用氨水:双氧水:去离子水混合比例为1:2:5配置第一溶液,将硅片放入第一溶液中清洗;采用盐酸:双氧水:去离子水混合比例为1:2:5配置第二溶液,将硅片放入第二溶液中清洗;最后将硅片于烘箱中烘烤去除表面的水分。As one of the preferred solutions of the present invention, the silicon wafer is cleaned before preparing the Six N dielectric layer. The specific steps are as follows: the first solution is prepared by using ammonia water: hydrogen peroxide: deionized water with a mixing ratio of 1:2:5, and the silicon wafer is Put it into the first solution for cleaning; use hydrochloric acid: hydrogen peroxide: deionized water with a mixing ratio of 1:2:5 to configure the second solution, put the silicon wafer into the second solution for cleaning; finally bake the silicon wafer in an oven to remove it surface moisture.

本发明利用聚焦离子束系统沉积铂电极,电极形状为锥形,底部尺寸较大为40~60nm(直径),与相变材料接触的电极顶部尺寸很小,为20nm以下,此种电极结构的优点主要是,首先可以将电极与相变材料接触的面积充分减小到20nm以下;其次电极底部的尺寸相对较大与底层电极材料的接触面积较大可以确保器件操作中底部各电极层材料间不会脱裂;第三,由于电极为锥形,沉积相变材料时有相对较大的接触面积(与垂直电极相比较),从而使得相变材料的生长更容易进行。The present invention utilizes a focused ion beam system to deposit a platinum electrode. The shape of the electrode is conical, and the size of the bottom is as large as 40-60 nm (diameter). The size of the top of the electrode in contact with the phase change material is very small, below 20 nm. The main advantages are that, firstly, the contact area between the electrode and the phase change material can be fully reduced to less than 20nm; secondly, the relatively large size of the bottom of the electrode and the large contact area with the bottom electrode material can ensure that the gap between the electrode layer materials at the bottom is relatively large during device operation. No detachment; third, because the electrodes are tapered, there is a relatively large contact area (compared with vertical electrodes) when depositing phase change materials, which makes the growth of phase change materials easier.

附图说明 Description of drawings

图1是本发明中在硅片衬底上制备一层SixN介质层的示意图;Fig. 1 is the schematic diagram of preparing one deck Six N dielectric layer on silicon chip substrate among the present invention;

图2是本发明中在SixN介质层上制备底层电极材料层的示意图;Fig. 2 is the schematic diagram of preparing the bottom electrode material layer on the Six N dielectric layer in the present invention;

图3是本发明中在底层电极材料层上制备氧化硅介质层的示意图;Fig. 3 is a schematic diagram of preparing a silicon oxide dielectric layer on the bottom electrode material layer in the present invention;

图4是本发明中在氧化硅介质层上制备氧化硅孔的示意图;Fig. 4 is a schematic diagram of preparing silicon oxide holes on a silicon oxide dielectric layer in the present invention;

图5是本发明中置备标记图形层的示意图;Fig. 5 is a schematic diagram of provisioning a mark graphics layer in the present invention;

图6是本发明中在氧化硅孔内利用聚焦离子束沉积铂制备锥形底电极的示意图;Fig. 6 is a schematic diagram of preparing a conical bottom electrode by using focused ion beam deposition of platinum in a silicon oxide hole in the present invention;

图7是本发明中在底电极上沉积相变材料层的示意图;7 is a schematic diagram of depositing a phase-change material layer on the bottom electrode in the present invention;

图8是本发明中在相变材料层上引出上层测试电极的示意图。Fig. 8 is a schematic diagram of drawing out the upper test electrode on the phase change material layer in the present invention.

具体实施方式 Detailed ways

下面结合附图进一步说明本发明的具体实施步骤:Further illustrate the specific implementation steps of the present invention below in conjunction with accompanying drawing:

硅片衬底清洗。清洗硅片:第一溶液:氨水:双氧水:去离子水=1:2:5,将硅片放入第一溶液中煮沸5分钟,冷却,去离子水冲洗3分钟,然后氮气吹干。主要作用是去除硅表面的油污和大颗粒。第二溶液:盐酸:双氧水:去离子水=1:2:5,将硅片放入第二溶液中清洗,方法同第一溶液中清洗,主要作用是去除硅片表面的金属离子,最后将硅片于120℃的烘箱中烘烤30min去除表面的水分。Silicon wafer substrate cleaning. Silicon wafer cleaning: first solution: ammonia water: hydrogen peroxide: deionized water = 1:2:5, put the silicon wafer into the first solution and boil for 5 minutes, cool, rinse with deionized water for 3 minutes, and then blow dry with nitrogen. The main function is to remove oil and large particles on the silicon surface. The second solution: hydrochloric acid: hydrogen peroxide: deionized water = 1:2:5, put the silicon chip into the second solution for cleaning, the method is the same as that of the first solution, the main function is to remove the metal ions on the surface of the silicon chip, and finally put The silicon wafers were baked in an oven at 120°C for 30 minutes to remove surface moisture.

如图1所示,SixN介质层的制备。利用化学气相沉积的方法在前述处理干净的硅片上沉积一层厚度为300~500nm的SixN。As shown in Figure 1, the preparation of the Six N dielectric layer. A layer of Six N with a thickness of 300-500 nm is deposited on the previously treated and cleaned silicon wafer by chemical vapor deposition.

如图2所示,底层电极材料层的制备。利用磁控溅射的方法形成底层电极Al/Ti/TiN,其相应的厚度控制为150nm/100nm/50nm。As shown in Figure 2, the preparation of the bottom electrode material layer. The bottom electrode Al/Ti/TiN is formed by magnetron sputtering, and its corresponding thickness is controlled to be 150nm/100nm/50nm.

如图3所示,底层电极材料层上氧化硅介质层的制备。利用离子束沉积法制备氧化硅介质层,氧化硅的厚度控制为100nm。As shown in FIG. 3 , a silicon oxide dielectric layer is prepared on the bottom electrode material layer. The silicon oxide dielectric layer is prepared by ion beam deposition, and the thickness of the silicon oxide is controlled to be 100nm.

如图4所示,氧化硅介质层上氧化硅孔的制备。旋涂电子束正性抗蚀剂,抗蚀剂厚度控制为150nm,执行电子束光刻形成50nm的光刻胶孔,利用反应离子刻蚀转移图形于氧化硅层,氧化硅孔的深度决定于氧化硅层的厚度,为保证孔内氧化硅完全去除需要刻蚀的氧化硅厚度最少为100~120nm,实际操作时可以适当的过刻,确保孔内的氧化硅完全去除。As shown in FIG. 4 , the silicon oxide holes on the silicon oxide dielectric layer are prepared. Electron beam positive resist is spin-coated, and the thickness of the resist is controlled to 150nm. Electron beam lithography is performed to form photoresist holes of 50nm, and reactive ion etching is used to transfer patterns to the silicon oxide layer. The depth of the silicon oxide holes is determined by The thickness of the silicon oxide layer is at least 100-120nm to be etched in order to ensure the complete removal of the silicon oxide in the holes. In actual operation, it can be properly over-etched to ensure the complete removal of the silicon oxide in the holes.

如图5所示,标记图形层的制备。利用聚焦离子束沉积铂制备标记图形层。标记图形的形状为十字线以及与之相连的四个方形组成;十字线的线宽为200nm,长度为2μm;方形尺寸为长度为1μm的正方形;标记层厚度为200nm。As shown in Figure 5, mark the preparation of the graphics layer. The marking pattern layer was prepared by depositing platinum by focused ion beam. The shape of the marking pattern is composed of a cross and four connected squares; the line width of the cross is 200nm and the length is 2μm; the size of the square is a square with a length of 1μm; the thickness of the marking layer is 200nm.

如图6所示,锥形底电极的制备。利用聚焦离子束沉积铂电极。电极底部直径控制为60nm以下,最好是50nm,顶部尺寸控制为20nm以下,电极高度至少为100nm。As shown in Figure 6, the preparation of the conical bottom electrode. Platinum electrodes are deposited using a focused ion beam. The diameter of the bottom of the electrode is controlled to be less than 60nm, preferably 50nm, the size of the top is controlled to be less than 20nm, and the height of the electrode is at least 100nm.

如图7所示,相变材料层的制备。利用磁控溅射结合剥离的方法沉积相变材料。旋涂正性双层电子束抗蚀剂,厚度控制为300nm,仔细精确的执行对准程序,而后电子光刻形成相变材料的沉积区域,区域尺寸为2×2μm;磁控溅射沉积厚度为100nm的相变材料,丙酮浸泡12小时剥离光刻胶及其上面沉积的相变材料。As shown in Figure 7, the phase change material layer is prepared. The phase change material was deposited by magnetron sputtering combined with stripping. Spin-coat positive double-layer electron beam resist, the thickness is controlled to 300nm, carefully and accurately perform the alignment procedure, and then electron lithography forms the deposition area of the phase change material, the area size is 2×2μm; magnetron sputtering deposition thickness For a 100nm phase change material, soak in acetone for 12 hours to strip off the photoresist and the phase change material deposited on it.

如图8所示,上层测试电极的引出。上层测试电极的沉积利用聚焦离子束沉积铂材料完成。电极的线宽控制为100nm以下,电极材料的厚度为100nm。As shown in Figure 8, the lead-out of the upper test electrode. Deposition of the upper test electrode was accomplished using focused ion beam deposition of platinum material. The line width of the electrode is controlled below 100nm, and the thickness of the electrode material is 100nm.

制备顶层绝热保护层,顶层沉积氧化硅作为顶层绝热保护层,采用离子束沉积法完成。氧化硅的厚度控制为200nm。Prepare the top thermal insulation protection layer, and deposit silicon oxide on the top layer as the top thermal insulation protection layer, which is completed by ion beam deposition. The thickness of silicon oxide is controlled to be 200nm.

本文中利用聚焦离子束系统沉积铂电极,电极形状为锥形,底部尺寸较大为40~60nm(直径),与相变材料接触的电极顶部尺寸很小,为20nm以下,此种电极结构的优点主要是,首先可以将电极与相变材料接触的面积充分减小到20nm以下;其次电极底部的尺寸相对较大与底层电极材料的接触面积较大可以确保器件操作中底部各电极层材料间不会脱裂;第三,由于电极为锥形,沉积相变材料时有相对较大的接触面积(与垂直电极相比较),从而使得相变材料的生长更容易进行。In this paper, a focused ion beam system is used to deposit a platinum electrode. The shape of the electrode is conical, and the size of the bottom is 40-60nm (diameter). The top of the electrode in contact with the phase change material is very small, below 20nm. The main advantages are that, firstly, the contact area between the electrode and the phase change material can be fully reduced to less than 20nm; secondly, the relatively large size of the bottom of the electrode and the large contact area with the bottom electrode material can ensure that the gap between the electrode layer materials at the bottom is relatively large during device operation. No detachment; third, because the electrodes are tapered, there is a relatively large contact area (compared with vertical electrodes) when depositing phase change materials, which makes the growth of phase change materials easier.

上述实施例仅用以说明而非限制本发明的技术方案。任何不脱离本发明精神和范围的技术方案均应涵盖在本发明的专利申请范围当中。The above embodiments are only used to illustrate but not limit the technical solution of the present invention. Any technical solutions that do not deviate from the spirit and scope of the present invention shall be included in the patent application scope of the present invention.

Claims (10)

1. the preparation method of a low power consumption phase changing memory is characterized in that, this method mainly may further comprise the steps:
1) preparation one deck Si on silicon chip substrate xThe N dielectric layer;
2) at Si xPreparation bottom electrode material layer on the N dielectric layer;
3) preparation silica medium layer on the bottom electrode material layer;
4) preparation silica hole on the silica medium layer;
5) in the silica hole, utilize the focused ion beam deposition metal to prepare cone bottom electrode;
6) sediment phase change material layer on cone bottom electrode;
7) on phase-change material layers, draw the upper strata test electrode.
2. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1, it is characterized in that: utilize the focused ion beam deposition metal to prepare cone bottom electrode in the step 5) in the silica hole, this metal comprises one or more in platinum, tungsten, titanium, gold, titanium nitride, the tungsten titanium.
3. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1 is characterized in that: the Si in the described step 1) xN dielectric layer, its thickness are 300~500nm.
4. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1 is characterized in that: described bottom electrode material layer is the bottom electrode Al/Ti/TiN that the method with magnetron sputtering forms, and its corresponding thickness is 150nm/100nm/50nm.
5. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1, it is characterized in that: the preparation in described silica hole utilizes the ion etching of electron beam exposure association reaction to finish, the diameter in silica hole is 40~60nm, and the degree of depth in hole is greater than the thickness of silica medium layer.
6. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1, it is characterized in that: described cone bottom electrode base diameter is 40~60nm, and the cone bottom electrode height is higher than the height in silica hole.
7. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1, it is characterized in that: the deposition of described phase-change material utilizes magnetron sputtering to finish in conjunction with peeling off, and promptly adopts acetone to soak behind the magnetron sputtering deposition phase-change material photoresist and the phase-change material that deposits above thereof are removed.
8. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1, it is characterized in that: described upper strata test electrode utilizes focused ion beam deposition platinum to draw, and the live width of extraction electrode is controlled to be below the 100nm, and thickness of electrode is 80nm.
9. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1; it is characterized in that: this method further is included in utilizes ion beam depositing method cvd silicon oxide to prepare the top layer heat-insulating protective layer on the test electrode of upper strata, the thickness of silica is 200nm.
10. the preparation method of a kind of low power consumption phase changing memory as claimed in claim 1 is characterized in that: at preparation Si xFirst cleaning silicon chip before the N dielectric layer, concrete steps are as follows: adopt ammoniacal liquor: hydrogen peroxide: the deionized water mixed proportion is that 1:2:5 disposes first solution, silicon chip is put into first solution clean; Adopt hydrochloric acid: hydrogen peroxide: the deionized water mixed proportion is that 1:2:5 disposes second solution, silicon chip is put into second solution clean; At last silicon chip is toasted the moisture of removing the surface in baking oven.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102544365A (en) * 2012-01-18 2012-07-04 北京大学 Resistance random access memory and manufacturing method thereof
CN103035840A (en) * 2012-12-19 2013-04-10 北京大学 Resistive random access memory and preparation method thereof
CN103779667A (en) * 2014-02-11 2014-05-07 国家纳米科学中心 Structural wave-absorbing material and manufacturing method thereof
CN105489755A (en) * 2015-12-03 2016-04-13 中国科学院半导体研究所 Self-aligned preparation method of full-limited phase-change memory with vertical structure
CN112002802A (en) * 2020-08-24 2020-11-27 华东师范大学 Preparation method of nano-sized tungsten plug small-electrode phase change memory device

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102544365A (en) * 2012-01-18 2012-07-04 北京大学 Resistance random access memory and manufacturing method thereof
CN103035840A (en) * 2012-12-19 2013-04-10 北京大学 Resistive random access memory and preparation method thereof
US9281476B2 (en) 2012-12-19 2016-03-08 Peking University Resistive memory and method for fabricating the same
CN103779667A (en) * 2014-02-11 2014-05-07 国家纳米科学中心 Structural wave-absorbing material and manufacturing method thereof
CN103779667B (en) * 2014-02-11 2016-02-03 国家纳米科学中心 A kind of structural absorbing mater ials and preparation method thereof
CN105489755A (en) * 2015-12-03 2016-04-13 中国科学院半导体研究所 Self-aligned preparation method of full-limited phase-change memory with vertical structure
CN105489755B (en) * 2015-12-03 2017-11-03 中国科学院半导体研究所 Vertical stratification limits the autoregistration preparation method of phase transition storage entirely
CN112002802A (en) * 2020-08-24 2020-11-27 华东师范大学 Preparation method of nano-sized tungsten plug small-electrode phase change memory device

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