201121034 六、發明說明: 【發明所屬之技術領域】 本發明係關於具有高的熱安定性之高輸出穿隧磁阻效 果元件及裝備了彼之低耗電非易失性磁記憶體。 【先前技術】 作爲被適用於將來的高集積度磁氣記憶體之穿隧磁阻 Q 效果元件’已被揭示了在可以得到比把鋁之氧化物用於絕 緣體之穿險磁阻效果兀件(T. Miyazaki and N. Tezuka, J. Magn. Magn. Mater. 139,L23 1 ( 1 995))更大數倍磁阻比之把 氧化鎂用於絕緣膜上的穿險磁阻效果元件(S. Yuasa. et al·,Nature Material 3,868(2004))。此外,從前的非易失 性磁氣記億體,係藉由在MO SFET上形成穿隧磁阻效果元 件之記憶胞而被構成的。開關(切換)是利用MOSFET,使 用藉由對位元線(bit line)與字線(word line)通電而產生的 〇 電流誘發之空間磁場而使穿隧磁阻效果元件之磁化方向旋 轉,寫入資訊,藉由穿隧磁阻效果元件之輸出電壓讀出資 訊的方式。此外,除了使用前述電流誘發的空間磁場之磁 化旋轉以外,還有藉由直接使電流流至磁阻效果元件使磁 化旋轉之所謂的自旋轉移力矩(spin transfer torque)磁化反 轉或者是同義之自旋注入磁化反轉方式,例如揭示於美國 專利第5,695,864號說明書或者日本特開2002-3 053 3 7號 公報。於日本特開2007-294737號公報,揭示了對來自外 部的侵入磁場在安定地使自旋轉移力矩(spin transfer -5- 201121034 torque)磁化反轉動作之目的下’適用了中介著非磁性膜而 層積的2層強磁性膜的記錄層之穿隧磁阻效果元件。 [先前技術文獻] [非專利文獻] [非專利文獻 1]J. Magn. Magn. Mater. 139, L23 1 (1 995) [非專利文獻 2]Nature Material 3,868(2004) [專利文獻] [專利文獻1]美國專利第5,695,864號說明書 [專利文獻2]日本專利特開2002-305337號公報 [專利文獻3]日本專利特開2007-294737號公報 【發明內容】 [發明所欲解決之課題] 要實現具有高可信賴性的低耗電量非易失性磁記憶體 ,必須要開發出在高輸出之穿隧磁阻效果元件之記錄層同 時滿足高的熱安定性,與自旋轉移力矩(spin transfer torque)磁化反轉之寫入方式的技術。 本發明之目的在於提供可以因應於這樣的要求之具有 高的熱安定性之穿隧磁阻效果元件及使用該元件之非易失 性磁記憶體。 [供解決課題之手段] 本發明,適用於在穿隧磁阻效果元件之強磁性膜適用 具有含硼的鈷或鐵之體心立方晶格之化合物強磁性膜,於· -6- 201121034 絕緣層適用(100)配向之岩鹽構造的氧化鎂,由挾著非磁性 導電層而設的第一擴散層與第二擴散層、鄰接於第一擴散 層的第一強磁性層與鄰接於第二擴散層的第二強磁性層所 構成,前述第一強磁性層與前述第二強磁性層係適用強磁 性結合的強磁性記錄層。亦即,根據本發明之穿隧磁阻效 果元件,具有絕緣層,及挾著絕緣層而被設置的強磁性記 錄層與強磁性固定層;絕緣層爲(1 0 0)配向之岩鹽構造的氧 0 化鎂膜,強磁性記錄層,係由挾著非磁性導電層而設的第 一擴散層與第二擴散層、鄰接於第一擴散層的第一強磁性 層與鄰接於第二擴散層的第二強磁性層所構成,前述第一 強磁性層鄰接於前述絕緣層,前述第二強磁性層與第一強 磁性層係強磁性結合著,強磁性固定層具有含鈷與鐵與硼 的體心立方構造之膜。 於絕緣層不使用(100)配向的岩鹽構造之氧化鎂膜的場 合,磁阻比顯著降低,磁記憶胞或磁隨機存取記憶體無法 〇 得到最低限度所必要的200mV之讀出電壓。 本發明之穿隧磁阻效果元件,可以適用於磁記憶胞或 磁隨機存取記憶體。 [發明之效果] 根據本發明,可得具有高的熱安定性,絕緣耐壓高的 穿隧磁阻效果元件。此外,藉由將該穿隧磁阻效果元件裝 備於磁記憶體,可以實現具有高的熱安定性,亦即磁氣資 訊的保持時間很長的非易失性記憶體。 201121034 【實施方式】 以下,參照圖面說明本發明之實施型態。在以下所述 之穿隧磁阻效果元件’其強磁性記錄層之磁化反轉(切換) 不是空間上的外部磁場’主要是藉由流動於穿隧磁阻效果 元件中的自旋偏極的電流之自旋對強磁性記錄層的磁矩 (electromagnetic moment)提供扭矩(torque)而進行的。此 自旋偏極的電流,在對穿隧磁阻效果元件流以電流時會自 體產生。亦即,藉由對穿隧磁阻效果元件由外部對穿隧磁 阻效果元件之各層的層積方向流以電流而使自旋轉移力矩 磁化反轉被實現。此外’藉由該電流的方向控制磁氣記錄 層的磁化方向,決定磁氣記錄層與磁氣固定層的磁化排列 。由磁氣記錄層使電流流至磁氣固定層的場合,磁氣固定 層與磁氣記錄層成爲平行排列,由磁氣固定層使電流流至 磁氣記錄層的場合,磁化排列成爲反平行排列。以下,把 自旋轉移力矩磁化反轉之引起的電流密度之閾値定義爲Jc [第1實施例] 圖1係顯示本發明的穿隧磁阻效果元件之一例之剖面 模式圖。在本實施例,穿隧磁阻效果元件1使用濺鍍法來 製作。此穿隧磁阻效果元件1,係由配向控制層3 09、反 強磁性層3 0 8、磁氣固定層3 0 5 1、絕緣層3 0 4、第一強磁 性層3 0 3、第一擴散層3 0 2 2、第一非磁性層3 0 2、第二擴 -8 - 201121034 散層3021、第二強磁性層301、保護層300來形成的。此 處,以第一強磁性層303、第一擴散層3022、第一非磁性 層302、第二擴散層3021、第二強磁性層301之層積構造 型成磁氣記錄層。磁氣固定層3 0 5 1亦有係以第四強磁性 層3 02、第二非磁性膜3 03、第三強磁性層3 04構成的場 合。 前述之穿隧磁阻效果元件’係藉由將圖3所示的層積 0 膜在330度以上〜420度以下的溫度進行熱處理而形成的 。圖3顯示在使用濺鍍法成膜而進行熱處理之前’或者是 被施加在3 3 0度以下之熱處理的穿隧磁阻效果元件,依照 配向控制層3 09、反強磁性層3 08、磁氣固定層305 1、絕 緣層3 04、第一強磁性層3 03、第一擴散層3022、第一非 磁性層302、第二擴散層3 02 1、第二強磁性層301 '保護 層3 00的順序被層積的。 配向控制層309係由NiFe形成的,但使用如Ta/NiFe Q 之2層膜、或者Ta/Ru/Ta/NiFe、Ta/NiFeCr等,可以提高 前述反強磁性層3 08的配向性,實現安定的反強磁性結合 的其他材料亦可。於反強磁性層3 08使用了 Mnlr(8nm) ’ 膜厚可在4〜15nm的範圍來選擇。此外,使用 MnPt、 MnFe等以錳化合物構成的反強磁性層亦可安定地實現反 強磁性結合。於第四強磁性層3 07使用CoFe(2nm),於第 二非磁性層3 06使用Ru(0.8mn),於第三強磁性層3 0 5使 用具有體心立方晶格的CoFeB(3nm)。此體心立方晶格的 CoFeB,在成膜時係非結晶之膜。於絕緣層適用(100)的氧 201121034 化鎂膜的場合,藉由330度以上的熱處理成膜時還是非結 晶的CoFeB進行結晶化而被形成爲體心立方晶格的CoFeB 。第四強磁性層307的CoFe的組成比係使鈷組成在50〜 9 0 a t m %之間。於此組成範圍,可以實現與前述反強磁性層 安定的反強磁性結合。第四強磁性層3 07、第二非磁性層 3 06、第三強磁性層3 05,選擇使第四強磁性層3 07與第三 強磁性層3 0 5之磁化進行反強磁性結合的材料,分別的膜 厚係以等於第四強磁性層3 07與第三強磁性層3 05的磁化 大小的方式選擇。 絕緣層3 04,係具有岩鹽構造的氧化鎂結晶膜,係在 (1〇〇)方向上配向度高的膜。此外,亦可爲完全配向於 (1 0 0)的單結晶膜。絕緣層的厚度爲0 · 6 n m〜3 n m之範圍。 藉由使絕緣層304的膜厚在前述範圍,於穿隧磁阻效果元 件1可以選擇任意的電阻。第一強磁性層3 03使用CoFeB ,藉由3 3 0度以上的熱處理而結晶化,與第三強磁性層 3 05的場合同樣得到體心立方晶格。第一強磁性層3 03與 第二強磁性層301之CoFeB之鈷與鐵的組成以在25 : 75 〜75 : 25之範圍爲佳。因爲在此組成範圍中體心立方構造 可安定地存在,且在適用氧化鎂於絕緣層3 04的穿隧磁阻 效果元件1,且可以提高對於穿隧磁阻比有所貢獻的自旋 分極率。第一非磁性層3 02以使用釕(Ru)爲佳。成膜時之 第一強磁性層/第一非磁性層/第二強磁性層使用的材料爲 CoFeB/Ru/CoFeB,藉由將此進行在3 3 0度以上的熱處理, 可以使在CoFeB中擴散了釕的CoFeB-Ru行成爲第一擴散 -10- 201121034 層與第二擴散層。該第一擴散層與第二擴散層的膜厚比第 一強磁性層與第二強磁性層更小,以在〇_2nm以上較佳。 在此膜厚時,第一強磁性層與第二強磁性層的磁化方向進 行平行結合。進而,進行3 3 0度以上的熱處理的結果,第 一強磁性層與第二強磁性層之磁化方向形成強磁性結合的 平行狀態。本實施例之熱處理時間以1小時以上較佳。 圖 7係如前述之例,顯示依照 Ta/Ru/Ta/NiFe/Mnlr/ Q CoFe/Ru/CoFeB/MgO/CoFeB/Ru/CoFeB/保護膜的順序層積 之穿隧磁阻效果元件在300 °C、325 °C、350 °C退火時之自旋 轉移力矩導致的磁化反轉之閾値電流密度與磁氣記錄層的 熱安定性的指標之E/kBT値對退火溫度(Ta)繪圖的結果》 根據此,Ta於3 50°C,E/kBT可得100以上之値。另一方 面,與Ta在3 3 0 °C以下的場合之E/kBT(60〜80)相比大幅 地提高。 圖8係爲了調查構成磁氣記錄層的第一強磁性層之 〇 C 〇 F eB與第二強磁性層之C 〇 F eB的磁化配列而測定之星狀 (asteroid)特性的退火溫度導致之變化。圖8(a)_i、(b)-l、 (c)-l顯示星狀(asteroid)特性。圖8(a)-l與圖8(b)-l之星 狀(asteroid)特性’分別如圖8(a)-2與圖8(b)-2所示意味 著第一強磁性層與第二強磁性層的磁化爲反平行狀態。另 一方面’ Ta = 3 5 0°C的場合’星狀特性如圖8(c)-l所示爲菱 側形狀。此係如圖8(c)-2所示意味著第一強磁性層與第二 強磁性層的磁化方向係中介著藉由35〇t退火而形成的第 一擴散層與第二擴散層與不擴散地殘留之第一非磁性層而 -11 - 201121034 平行排列的。或者是’意味著如圖8(c)_3所示’成膜時製 作的磁氣記錄層之非磁性層(R u)之全部擴散成爲一層之強 磁性層。亦即,圖7所示之Ta=3 5 0°c時之E/kBT的提高’ 被理解爲藉由磁氣記錄層成爲圖8(c)-2、圖8(c)_3所不的 構造而被實現的。此外’使用於第一強磁性層與第二強磁 性層的CoFeB在Ta = 35〇°C的場合結晶化而成爲體心立方 晶格的結晶的狀態。201121034 VI. Description of the Invention: [Technical Field] The present invention relates to a high output tunneling magnetoresistance effect element having high thermal stability and a low power consumption nonvolatile magnetic memory device equipped with the same. [Prior Art] As a tunneling magnetoresistive Q effect element applied to a high-concentration magnetic memory in the future, it has been revealed that a resistive magnetoresistance effect can be obtained by using an oxide of aluminum as an insulator. (T. Miyazaki and N. Tezuka, J. Magn. Magn. Mater. 139, L23 1 (1 995)) A magnetoresistance effect element with a larger number of times the magnetoresistance ratio of magnesium oxide used on an insulating film ( S. Yuasa. et al., Nature Material 3, 868 (2004)). Further, the former nonvolatile magnetic gas is constructed by forming a memory cell of a tunneling magnetoresistance effect element on the MO SFET. The switching (switching) is to use a MOSFET to rotate the magnetization direction of the tunneling magnetoresistive effect element by using a 〇 current-induced spatial magnetic field generated by energizing a bit line and a word line. Into the information, by means of the output voltage of the tunneling magnetoresistive effect element to read the information. Further, in addition to the magnetization rotation of the spatial magnetic field induced by the aforementioned current, there is also a so-called spin transfer torque magnetization reversal of magnetization rotation by directly causing a current to flow to the magnetoresistive effect element or is synonymous The spin-injection magnetization reversal method is disclosed, for example, in the specification of U.S. Patent No. 5,695,864 or JP-A-2002-3053. Japanese Laid-Open Patent Publication No. 2007-294737 discloses that an invasive magnetic field from the outside is used for the purpose of reversing the magnetization reversal action of spin transfer (5-201121034 torque). The tunneling magnetoresistance effect element of the recording layer of the laminated two-layer ferromagnetic film. [Prior Art Document] [Non-Patent Document] [Non-Patent Document 1] J. Magn. Magn. Mater. 139, L23 1 (1 995) [Non-Patent Document 2] Nature Material 3, 868 (2004) [Patent Document] [Patent Document 1] US Patent No. 5,695,864 [Patent Document 2] Japanese Patent Laid-Open Publication No. JP-A-2002-305337 (Patent Document No. JP-A-2007-294737) In order to realize a low-power non-volatile magnetic memory with high reliability, it is necessary to develop a recording layer of a high-output tunneling magnetoresistance effect element while satisfying high thermal stability and spin transfer. Spin transfer torque The technique of writing the magnetization reversal. SUMMARY OF THE INVENTION An object of the present invention is to provide a tunneling magnetoresistance effect element having high thermal stability in response to such a demand and a nonvolatile magnetic memory using the same. [Means for Solving the Problem] The present invention is applicable to a ferromagnetic film of a compound having a body-centered cubic lattice of cobalt or iron containing boron in a ferromagnetic film of a tunneling magnetoresistance effect element, and is insulated at -6-201121034 The layer is applied to (100) an oriented rock salt structure of magnesium oxide, a first diffusion layer and a second diffusion layer provided adjacent to the non-magnetic conductive layer, a first ferromagnetic layer adjacent to the first diffusion layer, and adjacent to the second The second ferromagnetic layer of the diffusion layer is configured, and the first ferromagnetic layer and the second ferromagnetic layer are applied to a ferromagnetic recording layer that is strongly magnetically bonded. That is, the tunneling magnetoresistance effect element according to the present invention has an insulating layer and a ferromagnetic recording layer and a ferromagnetic pinned layer provided next to the insulating layer; the insulating layer is a (100) aligned rock salt structure. An oxidized magnesium film, a ferromagnetic recording layer, a first diffusion layer and a second diffusion layer provided adjacent to the non-magnetic conductive layer, a first ferromagnetic layer adjacent to the first diffusion layer, and adjacent to the second diffusion a second ferromagnetic layer of the layer, the first ferromagnetic layer is adjacent to the insulating layer, the second ferromagnetic layer is strongly magnetically coupled to the first ferromagnetic layer, and the ferromagnetic pinned layer has cobalt and iron A membrane of body-centered cubic structure of boron. In the case where the insulating layer does not use the magnesium oxide film of the (100) aligned rock salt structure, the magnetoresistance ratio is remarkably lowered, and the magnetic memory cell or the magnetic random access memory cannot obtain the minimum necessary read voltage of 200 mV. The tunneling magnetoresistance effect element of the present invention can be applied to a magnetic memory cell or a magnetic random access memory. [Effects of the Invention] According to the present invention, a tunneling magnetoresistance effect element having high thermal stability and high insulation withstand voltage can be obtained. Further, by mounting the tunneling magnetoresistance effect element to the magnetic memory, it is possible to realize a nonvolatile memory having high thermal stability, that is, a long retention time of magnetic gas communication. [Embodiment] Hereinafter, embodiments of the present invention will be described with reference to the drawings. In the tunneling magnetoresistance effect element described below, the magnetization reversal (switching) of the ferromagnetic recording layer is not a spatial external magnetic field' mainly by the spin-polarity flowing in the tunneling magnetoresistance effect element. The spin of the current is supplied to the electromagnetic moment of the ferromagnetic recording layer to provide a torque. This spin-biased current is self-generated when current is applied to the tunneling magnetoresistive element. That is, the magnetization reversal of the spin transfer torque is realized by flowing a current through the stacking direction of the layers of the tunneling magnetoresistance effect elements to the tunneling magnetoresistance effect element. Further, the magnetization alignment of the magnetic recording layer and the magnetic gas fixing layer is determined by controlling the magnetization direction of the magnetic recording layer by the direction of the current. When the current is caused to flow to the magnetic gas fixed layer by the magnetic recording layer, the magnetic gas fixed layer and the magnetic gas recording layer are arranged in parallel, and when the magnetic gas fixed layer causes current to flow to the magnetic recording layer, the magnetization alignment becomes antiparallel. arrangement. In the following, the threshold 电流 of the current density due to the magnetization reversal of the spin transfer torque is defined as Jc. [First Embodiment] Fig. 1 is a cross-sectional view showing an example of the tunneling magnetoresistance effect element of the present invention. In the present embodiment, the tunneling magnetoresistance effect element 1 is fabricated by sputtering. The tunneling magnetoresistance effect element 1 is composed of an alignment control layer 3 09 , an antiferromagnetic layer 3 0 8 , a magnetic gas fixed layer 3 0 5 1 , an insulating layer 3 0 4 , a first ferromagnetic layer 3 0 3 , A diffusion layer 3 0 2 2, a first non-magnetic layer 3 0 2, a second extension -8 - 201121034, a dispersion layer 3021, a second ferromagnetic layer 301, and a protective layer 300 are formed. Here, a magnetic recording layer is formed by a laminated structure of the first ferromagnetic layer 303, the first diffusion layer 3022, the first non-magnetic layer 302, the second diffusion layer 3021, and the second ferromagnetic layer 301. The magnetic gas fixed layer 3 0 5 1 is also composed of a fourth ferromagnetic layer 302, a second non-magnetic film 303, and a third ferromagnetic layer 304. The tunneling magnetoresistance effect element ′ is formed by heat-treating the laminated 0 film shown in Fig. 3 at a temperature of 330 to 420 degrees. 3 shows a tunneling magnetoresistance effect element which is applied to a heat treatment of 340 degrees or less before being subjected to heat treatment by sputtering, according to the alignment control layer 3 09, the antiferromagnetic layer 3 08, and magnetic Gas fixing layer 305 1, insulating layer 304, first ferromagnetic layer 303, first diffusion layer 3022, first non-magnetic layer 302, second diffusion layer 301, second ferromagnetic layer 301 'protective layer 3 The order of 00 is layered. The alignment control layer 309 is formed of NiFe, but a two-layer film such as Ta/NiFe Q or Ta/Ru/Ta/NiFe, Ta/NiFeCr or the like can be used to improve the alignment of the antiferromagnetic layer 308. Other materials that are stable in anti-ferromagnetic bonding are also available. In the antiferromagnetic layer 3 08, Mnlr (8 nm) ’ film thickness can be selected in the range of 4 to 15 nm. Further, an antiferromagnetic layer composed of a manganese compound such as MnPt or MnFe can be stably achieved by antiferromagnetic bonding. CoFe (2 nm) is used for the fourth ferromagnetic layer 307, Ru (0.8 mn) is used for the second non-magnetic layer 306, and CoFeB (3 nm) having the body-centered cubic lattice is used for the third ferromagnetic layer 305. . The body-centered cubic lattice of CoFeB is a non-crystalline film at the time of film formation. When the oxygen layer 201121034 magnesium film is applied to the insulating layer, the film is formed into a body-centered cubic lattice CoFeB by crystallization of uncrystallized CoFeB when it is formed by heat treatment at 330 degrees or more. The composition ratio of CoFe of the fourth ferromagnetic layer 307 is such that the cobalt composition is between 50 and 90 a t m %. In this composition range, antiferromagnetic bonding with the aforementioned antiferromagnetic layer stability can be achieved. The fourth ferromagnetic layer 307, the second non-magnetic layer 306, and the third ferromagnetic layer 305 are selected to be antiferromagnetically combined with the magnetization of the fourth ferromagnetic layer 307 and the third ferromagnetic layer 305. The material, the respective film thicknesses are selected in a manner equal to the magnetization of the fourth ferromagnetic layer 307 and the third ferromagnetic layer 305. The insulating layer 304 is a magnesium oxide crystal film having a rock salt structure and is a film having a high degree of alignment in the (1 〇〇) direction. Further, it may be a single crystal film which is completely aligned with (100). The thickness of the insulating layer is in the range of 0 · 6 n m to 3 n m. By making the film thickness of the insulating layer 304 within the above range, an arbitrary resistance can be selected in the tunneling magnetoresistance effect element 1. The first ferromagnetic layer 303 is crystallized by heat treatment of 340 degrees or more using CoFeB, and a body-centered cubic lattice is obtained in the same manner as in the case of the third ferromagnetic layer 305. The composition of cobalt and iron of CoFeB of the first ferromagnetic layer 303 and the second ferromagnetic layer 301 is preferably in the range of 25:75 to 75:25. Since the body-centered cubic structure can be stably present in this composition range, and the tunneling magnetoresistance effect element 1 of magnesium oxide in the insulating layer 304 is applied, and the spin polarization which contributes to the tunneling magnetoresistance ratio can be improved. rate. The first non-magnetic layer 322 is preferably ruthenium (Ru). The material used for the first ferromagnetic layer/first non-magnetic layer/second ferromagnetic layer at the time of film formation is CoFeB/Ru/CoFeB, which can be made in CoFeB by heat treatment at 340 degrees or higher. The CoFeB-Ru line diffused with yttrium becomes the first diffusion -10- 201121034 layer and the second diffusion layer. The film thickness of the first diffusion layer and the second diffusion layer is smaller than that of the first ferromagnetic layer and the second ferromagnetic layer, and is preferably 〇_2 nm or more. At this film thickness, the magnetization directions of the first ferromagnetic layer and the second ferromagnetic layer are parallel-bonded. Further, as a result of the heat treatment of 340 degrees or more, the magnetization directions of the first ferromagnetic layer and the second ferromagnetic layer form a parallel state of strong magnetic bonding. The heat treatment time in this embodiment is preferably 1 hour or more. Figure 7 is a diagram showing the tunneling magnetoresistance effect element in accordance with the sequential lamination of Ta/Ru/Ta/NiFe/Mnlr/Q CoFe/Ru/CoFeB/MgO/CoFeB/Ru/CoFeB/protective film as in the foregoing example. The threshold of the magnetization reversal caused by the spin transfer torque at °C, 325 °C, and 350 °C, and the E/kBT値 of the thermal stability of the magnetic recording layer are plotted against the annealing temperature (Ta). Results According to this, Ta at 3 50 ° C, E / kBT can get more than 100. On the other hand, it is greatly improved compared with E/kBT (60 to 80) where Ta is below 330 °C. Figure 8 is a graph showing the annealing temperature of asteroid characteristics measured in order to investigate the magnetization arrangement of 〇C 〇F eB of the first ferromagnetic layer constituting the magnetic recording layer and C 〇F eB of the second ferromagnetic layer. Variety. Figures 8(a)_i, (b)-l, (c)-l show asteroid characteristics. The asteroid characteristics of Fig. 8(a)-1 and Fig. 8(b)-1 are as shown in Figs. 8(a)-2 and 8(b)-2, respectively, indicating the first ferromagnetic layer and The magnetization of the second ferromagnetic layer is in an anti-parallel state. On the other hand, the case where 'Ta = 3 50 ° C' is a rhombic shape as shown in Fig. 8 (c) - l. This is shown in FIG. 8(c)-2, which means that the magnetization directions of the first ferromagnetic layer and the second ferromagnetic layer are interposed by the first diffusion layer and the second diffusion layer formed by annealing at 35 〇t. The first non-magnetic layer remaining without diffusion and -11 - 201121034 are arranged in parallel. Alternatively, it means that the non-magnetic layer (R u) of the magnetic recording layer formed at the time of film formation as shown in Fig. 8 (c) - 3 is diffused into a strong magnetic layer of one layer. That is, the improvement of E/kBT at Ta = 3 50 °c shown in Fig. 7 is understood to be that the magnetic recording layer becomes as shown in Figs. 8(c)-2 and 8(c)_3. Constructed and implemented. Further, the CoFeB used in the first ferromagnetic layer and the second strong magnetic layer is crystallized at a Ta = 35 〇 °C to form a crystal of the body center cubic lattice.
CoFeB之硼的組成比,以結晶化變成安定的硼組成在 10〜30atm%之間爲佳。進而,在第一強磁性層303、第二 強磁性層301除了 CoFeB以外,使用CoFe之單層膜、NiFe 之單層膜、CoFe/NiFe 或 CoFeB/NiFe 進而包括 CoFeB/CoFe 之2層膜亦可。保護層3 00係以Ta(5nm)/RU(5nni)之2層膜 形成的。 [第2實施例] 圖2係於根據本發明之穿隧磁阻效果元件2,成膜時 之第一非磁性層藉由3 3 0 °C以上之熱處理而全部擴散至第 一強磁性層與第二強磁性層,形成一層之擴散強磁性層之 例之剖面模式圖。此穿隧磁阻效果元件2,係由配向控制 層309、反強磁性層308、磁氣固定層3051、絕緣層304 、擴散強磁性層3 0 1 2、保護層3 0 0而形成的。磁氣固定層 3 05 1亦有係以第四磁性層3 07、第二非磁性層3 06、第三 強磁性層305構成的場合。 前述之穿隧磁阻效果元件2,與在第1實施例所示之 -12- 201121034 穿隧磁阻效果元件1的製作方法相同,係藉由將圖3所示 的層積膜在3 3 0度以上〜420度以下的溫度進行熱處理而 形成的。 於穿隧磁阻效果元件2,也與穿隧磁阻效果元件1同 樣如圖7所示於Ta = 35(TC可以實現1〇〇以上之E/kT。於 成膜時之第一強磁性層與第二強磁性層使用CoFeB,於第 一非磁性層使用Ru的場合更佳,藉由3 3 0 °C以上之退火最 0 終形成的擴散強磁性層爲C〇FeBRu。 [第3實施例] 圖3顯示於圖1之穿隧磁阻效果元件1具有磁氣固定 層與磁氣記錄層的層積順序相反的構成之穿隧磁阻效果元 件3。 在本實施例如圖6所示,把依照配向控制膜3 09、第 二強磁性層3 0 1、第一非磁性層3 02、第一強磁性層3 0 3、 〇 絶縁層3 〇4、第三強磁性層3 05、第二非磁性層3 06、第四 強磁性層3 07、反強磁性層3 08、保護層3 00之順序層積 的層積膜,於3 3 (TC進行熱處理而形成的。 於藉由本實施例形成的穿隧磁阻效果元件3,也與穿 隧磁阻效果元件1及穿隧磁阻效果元件2同樣,如圖7所 示可以於Ta = 3 50°C實現1〇〇以上之E/kT。 第一非磁性層3 02以使用釕(Ru)爲佳。成膜時之第一 強磁性層/第一非磁性層/第二強磁性層使用的材料爲 CoFeB/Ru/CoFeB,藉由將此進行在330度以上的熱處理, -13- 201121034 可以使在CoFeB中擴散了釕的CoFeB-Ru形成爲第一擴散 層與第二擴散層。該第一擴散層與第二擴散層的膜厚比第 一強磁性層與第二強磁性層更小,以在0.2 nm以上較佳。 在此膜厚時,第一強磁性層與第二強磁性層的磁化方向進 行平行結合。進而,進行330度以上的熱處理的結果,第 一強磁性層與第二強磁性層之磁化方向形成強磁性結合的 平行狀態。本實施例之熱處理時間以1小時以上較佳。 €) [第4實施例]The composition ratio of boron of CoFeB is preferably from 10 to 30 atm% in terms of crystallization to a stable boron composition. Further, in the first ferromagnetic layer 303 and the second ferromagnetic layer 301, in addition to CoFeB, a single layer film of CoFe, a single layer film of NiFe, CoFe/NiFe or CoFeB/NiFe, and a two-layer film of CoFeB/CoFe are also used. can. The protective layer 300 is formed of a two-layer film of Ta (5 nm) / RU (5 nni). [Second Embodiment] Fig. 2 is a tunneling magnetoresistance effect element 2 according to the present invention, in which a first non-magnetic layer is entirely diffused to a first ferromagnetic layer by heat treatment at a temperature of 30 ° C or higher. A cross-sectional pattern diagram of an example of a diffusion ferromagnetic layer formed with a second ferromagnetic layer. The tunneling magnetoresistance effect element 2 is formed by an alignment control layer 309, an antiferromagnetic layer 308, a magnetic gas fixed layer 3051, an insulating layer 304, a diffusion ferromagnetic layer 3 0 1 2, and a protective layer 300. The magnetic gas fixed layer 305 1 is also composed of the fourth magnetic layer 307, the second non-magnetic layer 306, and the third ferromagnetic layer 305. The tunneling magnetoresistance effect element 2 described above is the same as the method of manufacturing the tunneling magnetoresistive effect element 1 of the -12-201121034 shown in the first embodiment, by laminating the laminated film shown in FIG. It is formed by heat treatment at a temperature of 0 degrees or more to 420 degrees or less. The tunneling magnetoresistance effect element 2 is also the same as the tunneling magnetoresistance effect element 1 as shown in Fig. 7 at Ta = 35 (TC can achieve E/kT of 1 〇〇 or more. The first ferromagnetism at the time of film formation) CoFeB is used for the layer and the second ferromagnetic layer, and Ru is preferably used for the first non-magnetic layer, and the diffusion ferromagnetic layer formed by the annealing at 305 ° C or higher is C〇FeBRu. [Embodiment] FIG. 3 shows a tunneling magnetoresistance effect element 1 having a reversed order of lamination of a magnetic gas fixed layer and a magnetic recording layer in the tunneling magnetoresistance effect element 1 of FIG. 1. In this embodiment, for example, FIG. According to the alignment control film 309, the second ferromagnetic layer 301, the first non-magnetic layer 312, the first ferromagnetic layer 030, the 縁3 〇4, and the third ferromagnetic layer 3 05 a laminated film in which the second non-magnetic layer 306, the fourth ferromagnetic layer 307, the antiferromagnetic layer 308, and the protective layer 00 are sequentially laminated is formed by heat treatment at 3 3 (TC). The tunneling magnetoresistance effect element 3 formed by the present embodiment is also the same as the tunneling magnetoresistive effect element 1 and the tunneling magnetoresistance effect element 2, as shown in FIG. 7 at Ta = 3 50°. C realizes E/kT of 1 〇〇 or more. The first non-magnetic layer 312 is preferably ruthenium (Ru). The first ferromagnetic layer/first non-magnetic layer/second strong magnetic layer used in film formation is used. The material is CoFeB/Ru/CoFeB, and by performing heat treatment at 330 degrees or higher, -13-201121034, CoFeB-Ru diffused with ruthenium in CoFeB can be formed into a first diffusion layer and a second diffusion layer. The film thickness of a diffusion layer and the second diffusion layer is smaller than that of the first ferromagnetic layer and the second ferromagnetic layer, and is preferably 0.2 nm or more. In the film thickness, the first ferromagnetic layer and the second ferromagnetic layer The magnetization direction of the layer is parallel-bonded. Further, as a result of heat treatment of 330 degrees or more, the magnetization directions of the first ferromagnetic layer and the second ferromagnetic layer form a parallel state of strong magnetic bonding. The heat treatment time in this embodiment is 1 hour. The above is preferred. €) [Fourth Embodiment]
圖4顯示於圖2之穿隧磁阻效果元件2具有磁氣固定 層與磁氣記錄層的層積順序相反的構成之穿隧磁阻效果元 件4。此穿隧磁阻效果元件4,係由配向控制層3 09、反強 磁性層3 08、擴散強磁性層301、絕緣層3 04、磁氣固定層 3 0 5 1、保護層3 0 0而形成的。磁氣固定層3 0 5 1亦有係以 第四強磁性層307、第二非磁性層3 06、第三強磁性層3〇5 構成的場合。 Q 前述之穿隧磁阻效果元件4,與在第2實施例所示之 穿隧磁阻效果元件1的製作方法相同,係藉由將圖6所示 的層積膜在3 3 0 °C以上〜4 2 0 °C以下的溫度進行熱處理而形 成的。於穿隧磁阻效果元件2,也與穿隧磁阻效果元件1 同樣如圖7所示於Ta = 350°C可以實現1〇〇以上之E/kT。 於成膜時之第一強磁性層與第二強磁性層使用CoFeB,於 第一非磁性層使用Ru的場合更佳,藉由3 3 0°C以上之退火 最終形成的擴散強磁性層爲CoFeBRu。 -14- 201121034 圖9與圖10係顯示根據本發明之磁記憶胞的構成例 之剖面模式圖。此磁記憶胞,作爲記憶胞搭載了第1實施 例至第4實施例所示的穿隧磁阻效果元件200。圖9係特 徵爲穿隧磁阻效果元件200被形成於由源極電極102升起 的電極上,圖1 0係穿隧磁阻效果元件200形成於由源極 電極102之層積上拉出電極400而被形成的。 C-MOS100係由2個η型半導體101、102與一個p型 Q 半導體103所構成。於η型半導體ιοί被導電連接成爲汲 極的電極121,中介著電極141及電極147被接地。於η 型半導體102,被導電連接著成爲源極的電極122。進而 ,123爲閘極電極,藉由此閘極電極123的打開/關閉而控 制源極電極122與汲極電極121間的電流之打開/關閉。 於前述源極電極122被層積電極145、電極144、電極143 、電極M2,中介著電極400被連接著穿隧磁阻效果元件 2 0的配向控制膜3 0 9。 Ο 位元線40 1被連接於前述穿隧磁阻效果元件200的保 護膜3 〇〇。在本實施例之磁記憶胞,流至穿隧磁阻效果元 件200的電流,藉由所謂的自旋轉移力矩(spin transfer torque)而使穿隧磁阻效果元件200之強磁性記錄層的磁化 方向旋轉而記錄磁氣資訊。自旋轉移力矩不是空間上的外 部磁場’主要是流動於穿隧磁阻效果元件中的自旋偏極的 電流之自旋對穿隧磁阻效果元件之強磁性記錄層的磁矩 (electromagnetic moment)提供扭矩(torque)的原理。此自 旋ί扁極的電流具有在對穿隧磁阻效果元件流以電流時在自 -15- 201121034 身產生的機制。亦即,具有對穿隧磁阻效果元件由外部供 給電流的手段,藉由從該手段流以電流而使自旋轉移力矩 磁化反轉被實現。藉由該電流的方向控制磁氣記錄層的磁 化方向,決定磁氣記錄層與磁氣固定層的磁化排列。在本 實施例,藉由使用 C-MOS 100,而把流至穿隧磁阻效果元 件2 0 0的電流的方向設定爲雙方向。由磁氣記錄層使電流 流至磁氣固定層的場合,磁氣固定層與磁氣記錄層成爲平 行排列,由磁氣固定層使電流流至磁氣記錄層的場合,磁 化排列成爲反平行排列。在本實施例,藉由在位元線2 1 2 與電極47之間使電流流過而對穿隧磁阻效果元件200中 的強磁性記錄層作用自旋轉移力矩(spin transfer torque)。 藉由自旋轉移力矩進行寫入的場合,寫入時的電力與使用 電流磁場的場合相比可以減低至百分之一的程度。此外, 藉由裝備具有100以上之E/kT的穿隧磁阻效果元件200, 可以實現可構成十億位元(gigabits)之磁記億體的磁記億胞 〇 圖11係顯示配置前述磁記憶胞的磁隨機存取記憶體 的構成例。閘極電極1 2 3與位元線4 0 1被導電連接於記憶 胞500 °藉由配置記載於前述實施例的磁記憶胞前述磁記 憶體可在低耗電量下動作,可以實現十億位元級的高密度 磁記憶體。 【圖式簡單說明】 圖1係顯示本發明之穿隧磁阻效果元件'之第一構成例。 -16- 201121034 圖2係顯示本發明之穿隧磁阻效果元件之第二構成例。 圖3係顯示本發明之穿隧磁阻效果元件之第三構成例。 圖4係顯示本發明之穿隧磁阻效果元件之第四構成例。 圖5係顯示本發明之穿隧磁阻效果元件之第一、第二 構成之成膜之後的構成例。 圖6係顯示本發明之穿隧磁阻效果元件之第三、第四 構成之成膜之後的構成例。 0 圖7係顯示本發明之穿隧磁阻效果元件之寫入電流(a) 、熱安定性(b)之熱處理溫度依存性例。 圖8係顯示本發明之穿隧磁阻效果元件之星狀 (asteroid)特性與磁氣記錄層之層積狀態的熱處理溫度依存 性。 圖9係顯示本發明之磁記憶胞的構成例。 圖1 0係顯示本發明之磁記憶胞的構成例。 圖1 1係顯示本發明之磁隨機存取記億體的構成例。 【主要元件符號說明】 1 :穿隧磁阻效果元件 2 :穿隧磁阻效果元件 3 :穿隧磁阻效果元件 4 :穿隧磁阻效果元件 5 :穿隧磁阻效果元件Fig. 4 shows the tunneling magnetoresistance effect element 2 of Fig. 2 having a tunneling magnetoresistance effect element 4 having a reversed order of lamination of a magnetic gas fixed layer and a magnetic gas recording layer. The tunneling magnetoresistance effect element 4 is composed of an alignment control layer 309, an antiferromagnetic layer 308, a diffusion ferromagnetic layer 301, an insulating layer 304, a magnetic gas fixed layer 3 0 5 1 , and a protective layer 300. Forming. The magnetic gas fixed layer 3 0 5 1 is also composed of the fourth ferromagnetic layer 307, the second non-magnetic layer 306, and the third ferromagnetic layer 3〇5. Q The tunneling magnetoresistance effect element 4 is the same as the tunneling magnetoresistance effect element 1 shown in the second embodiment, and the laminated film shown in FIG. 6 is at 3 30 ° C. It is formed by heat treatment at a temperature of ~40 ° C or lower. Similarly to the tunneling magnetoresistance effect element 2, as shown in Fig. 7, the tunneling magnetoresistance effect element 2 can achieve E/kT of 1 〇〇 or more at Ta = 350 °C. CoFeB is used for the first ferromagnetic layer and the second ferromagnetic layer during film formation, and Ru is preferably used for the first non-magnetic layer, and the diffusion ferromagnetic layer finally formed by annealing at 340 ° C or higher is CoFeBRu. -14- 201121034 Fig. 9 and Fig. 10 are cross-sectional schematic views showing a configuration example of a magnetic memory cell according to the present invention. In the magnetic memory cell, the tunneling magnetoresistance effect element 200 shown in the first to fourth embodiments is mounted as a memory cell. 9 is characterized in that the tunneling magnetoresistance effect element 200 is formed on an electrode raised by the source electrode 102, and the tunneling magnetoresistive effect element 200 is formed on the layer of the source electrode 102. The electrode 400 is formed. The C-MOS 100 is composed of two n-type semiconductors 101 and 102 and one p-type Q semiconductor 103. The n-type semiconductor ιοί is electrically connected to the electrode 121 of the drain, and the electrode 141 and the electrode 147 are grounded. The n-type semiconductor 102 is electrically connected to the electrode 122 serving as a source. Further, 123 is a gate electrode, and the opening/closing of the current between the source electrode 122 and the drain electrode 121 is controlled by the opening/closing of the gate electrode 123. The source electrode 122 is laminated with the electrode 145, the electrode 144, the electrode 143, and the electrode M2, and the interposing electrode 400 is connected to the alignment control film 309 of the tunneling magnetoresistance effect element 20. The Ο bit line 40 1 is connected to the protective film 3 前述 of the tunneling magnetoresistance effect element 200 described above. In the magnetic memory cell of the present embodiment, the current flowing to the tunneling magnetoresistance effect element 200 causes the magnetization of the ferromagnetic recording layer of the tunneling magnetoresistive effect element 200 by a so-called spin transfer torque. The direction is rotated to record the magnetic gas information. The spin transfer torque is not the external magnetic field in space 'mainly the spin of the current flowing through the spin bias in the tunneling magnetoresistance effect element. The magnetic moment of the ferromagnetic recording layer of the tunneling magnetoresistive effect element (electromagnetic moment) ) Provide the principle of torque. This spin ί flat current has a mechanism generated from the body of -15-201121034 when current is flowing to the tunneling magnetoresistive effect element. That is, a means for supplying a current to the tunneling magnetoresistance effect element from the outside is realized by causing a current from the means to cause magnetization reversal of the spin transfer torque. The magnetization alignment of the magnetic recording layer and the magnetic gas fixed layer is determined by controlling the magnetization direction of the magnetic recording layer by the direction of the current. In the present embodiment, the direction of the current flowing to the tunneling magnetoresistance effect element 200 is set to the two directions by using the C-MOS 100. When the current is caused to flow to the magnetic gas fixed layer by the magnetic recording layer, the magnetic gas fixed layer and the magnetic gas recording layer are arranged in parallel, and when the magnetic gas fixed layer causes current to flow to the magnetic recording layer, the magnetization alignment becomes antiparallel. arrangement. In the present embodiment, a spin transfer torque is applied to the ferromagnetic recording layer in the tunneling magnetoresistive effect element 200 by flowing a current between the bit line 2 1 2 and the electrode 47. When writing is performed by a rotational torque, the electric power at the time of writing can be reduced to one percent as compared with the case of using a current magnetic field. In addition, by equipping the tunneling magnetoresistance effect element 200 having an E/kT of 100 or more, it is possible to realize a magnetic memory cell which can constitute a gigabits. FIG. 11 shows that the magnetic body is arranged. A configuration example of a magnetic random access memory of a memory cell. The gate electrode 1 2 3 and the bit line 4 0 1 are electrically connected to the memory cell 500 °. By arranging the magnetic memory cell described in the foregoing embodiment, the magnetic memory can operate at a low power consumption, and can realize one billion. High-density magnetic memory in the bit level. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a view showing a first configuration example of a tunneling magnetoresistance effect element of the present invention. -16- 201121034 Fig. 2 shows a second configuration example of the tunneling magnetoresistive effect element of the present invention. Fig. 3 is a view showing a third configuration example of the tunneling magnetoresistance effect element of the present invention. Fig. 4 is a view showing a fourth configuration example of the tunneling magnetoresistance effect element of the present invention. Fig. 5 is a view showing a configuration example after film formation of the first and second structures of the tunneling magnetoresistance effect element of the present invention. Fig. 6 is a view showing a configuration example after film formation of the third and fourth configurations of the tunneling magnetoresistance effect element of the present invention. Fig. 7 is a view showing an example of the heat treatment temperature dependence of the write current (a) and the thermal stability (b) of the tunneling magnetoresistance effect element of the present invention. Fig. 8 is a graph showing the heat treatment temperature dependence of the asteroid characteristics of the tunneling magnetoresistance effect element of the present invention and the laminated state of the magnetic recording layer. Fig. 9 is a view showing an example of the configuration of a magnetic memory cell of the present invention. Fig. 10 shows a configuration example of a magnetic memory cell of the present invention. Fig. 1 is a view showing an example of the configuration of a magnetic random access memory of the present invention. [Description of main component symbols] 1 : Tunneling magnetoresistance effect element 2 : Tunneling magnetoresistance effect element 3 : Tunneling magnetoresistance effect element 4 : Tunneling magnetoresistance effect element 5 : Tunneling magnetoresistance effect element
6 :穿隧磁阻效果元件 100 : C-M0S -17- 201121034 101 :第一 η型半導體 102:第二η型半導體 103 : ρ型半導體 1 2 2 :源極電極 4 0 1 ·位兀線 1 2 1 :汲極電極 1 2 3 :閘極電極 3 0 9 :配向控制膜 3 0 8 :反強磁性層 3051 :磁氣固定層 3 0 7 :第四強磁性層 3 0 6 :第二非磁性層 3 0 5 :第三強磁性層 3 0 4 :絕緣層 3 0 3 :第一強磁性層 3 0 2 :第一非磁性層 3 0 1 :第二強磁性層 3 00 :保護層 3 0 1 1 :磁氣記錄層 3 0 1 2 :擴散強磁性層 3 0 2 1 :第二擴散層 3 0 2 2 :第一擴散層 1 4 1 :電極配線 1 4 2 :電極配線 -18 201121034 1 4 3 :電極配線 144 :電極配線 1 4 5 :電極配線 1 4 6 :電極配線 〇6: tunneling magnetoresistance effect element 100: C-M0S -17- 201121034 101: first n-type semiconductor 102: second n-type semiconductor 103: p-type semiconductor 1 2 2 : source electrode 4 0 1 · bit line 1 2 1 : drain electrode 1 2 3 : gate electrode 3 0 9 : alignment control film 3 0 8 : antiferromagnetic layer 3051 : magnetic gas fixed layer 3 0 7 : fourth strong magnetic layer 3 0 6 : second Non-magnetic layer 3 0 5 : third ferromagnetic layer 3 0 4 : insulating layer 3 0 3 : first ferromagnetic layer 3 0 2 : first non-magnetic layer 3 0 1 : second ferromagnetic layer 3 00 : protective layer 3 0 1 1 : magnetic gas recording layer 3 0 1 2 : diffusion ferromagnetic layer 3 0 2 1 : second diffusion layer 3 0 2 2 : first diffusion layer 1 4 1 : electrode wiring 1 4 2 : electrode wiring -18 201121034 1 4 3 : Electrode wiring 144 : Electrode wiring 1 4 5 : Electrode wiring 1 4 6 : Electrode wiring 〇