TW201735358A - Semiconductor element and electric apparatus using same - Google Patents

Semiconductor element and electric apparatus using same Download PDF

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TW201735358A
TW201735358A TW105142985A TW105142985A TW201735358A TW 201735358 A TW201735358 A TW 201735358A TW 105142985 A TW105142985 A TW 105142985A TW 105142985 A TW105142985 A TW 105142985A TW 201735358 A TW201735358 A TW 201735358A
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semiconductor
layer
electrode
semiconductor layer
schottky
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TWI751999B (en
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霍間勇輝
関谷隆司
笘井重和
川嶋絵美
上岡義弘
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出光興產股份有限公司
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Abstract

A semiconductor element 1 is characterized by comprising: a pair of an ohmic electrode 20 and a Schottky electrode 10 separated from each other; and a semiconductor layer 30 in contact with the ohmic electrode 20 and the Schottky electrode 10, wherein formula (I) is satisfied (in the formula, n represents the carrier concentration (cm-3) of the semiconductor layer, [epsilon] represents the dielectric constant (F/cm) of the semiconductor layer, Ve represents the forward effective voltage (V) between the ohmic electrode and the Schottky electrode, q represents the elementary charge (C), L represents the distance (cm) between the ohmic electrode and the Schottky electrode).

Description

半導體元件及使用其之電氣機器Semiconductor component and electrical machine using the same

本發明係關於一種半導體元件以及使用其之肖特基能障二極體、接面電晶體、電子電路及電氣機器。The present invention relates to a semiconductor device and a Schottky barrier diode, junction transistor, electronic circuit, and electrical machine using the same.

作為實現大電流、低耗電之功率半導體材料,以Si為代表,可列舉SiC、GaN等新材料。又,氧化鎵、金剛石亦作為下一代材料而受到關注。另一方面,因該等材料基本上係以單晶形式加以利用,故而具有難以於異質基板上單晶生長,基板之選擇受到限制之缺點。 關於SiC,作為功率半導體較佳之結晶構造為4H-SiC,且絕緣破壞電場實現了3 MV/cm以上。然而,因晶格之失配較大,故難以於Si上使缺陷較少之單晶良率較好地磊晶生長。若為3C-SiC,則可藉由對Si晶圓實施微細加工,或使用Si(211)面而進行磊晶生長,但帶隙變窄,故絕緣破壞電場限於1.2 MV/cm。又,GaN亦與4H-SiC同樣地絕緣破壞電場為3 MV/cm以上,且為實現量產而嘗試了於Si上進行結晶生長。然而,雖然就與Si之晶格失配之方面而言並未達到如SiC般之程度,但若不介隔AIN等緩衝層,則結晶難以生長,於量產性方面存在問題。 因此,正在對如專利文獻1般之實現與使用多晶或非晶之氧化物半導體之異質基板匹配之功率器件展開研究。通常,如非專利文獻1所揭示,於單極之功率器件中,為獲得最低導通電阻,下述式之關係成立,且若耐壓設計及半導體材料種類確定,則最佳載子濃度得以確定。然而,非晶或多晶半導體難以控制載子濃度。 [數1](式中,εs 為材料之介電常數,Ec 為最大絕緣破壞電場,q為基本電荷,BV為作為設計值之耐壓,ND 為載子濃度) 先前技術文獻 專利文獻 專利文獻1:WO2015/025499A1 非專利文獻 非專利文獻1:“ Fundamentals of Power Semiconductor Devices”, B. Jayant Baliga, Springer Science & Business Media, 2010/04/02As a power semiconductor material that realizes a large current and a low power consumption, a new material such as SiC or GaN is exemplified as Si. Moreover, gallium oxide and diamond have also attracted attention as next-generation materials. On the other hand, since these materials are basically used in a single crystal form, there is a disadvantage that it is difficult to grow a single crystal on a heterogeneous substrate, and the selection of the substrate is limited. Regarding SiC, a preferred crystal structure as a power semiconductor is 4H-SiC, and the dielectric breakdown electric field is 3 MV/cm or more. However, since the mismatch of the crystal lattice is large, it is difficult to epitaxially grow the single crystal having a small defect on Si. In the case of 3C-SiC, epitaxial growth can be performed by performing microfabrication on the Si wafer or Si (211) plane, but the band gap is narrowed, so the dielectric breakdown electric field is limited to 1.2 MV/cm. Further, GaN also has an insulation breakdown electric field of 3 MV/cm or more similarly to 4H-SiC, and attempts to carry out crystal growth on Si in order to achieve mass production. However, although it is not as good as SiC in terms of lattice mismatch with Si, if the buffer layer such as AIN is not interposed, crystal growth is difficult, and there is a problem in mass productivity. Therefore, research is being conducted on a power device that is compatible with a hetero-substrate using a polycrystalline or amorphous oxide semiconductor as in Patent Document 1. In general, as disclosed in Non-Patent Document 1, in a unipolar power device, in order to obtain the lowest on-resistance, the relationship of the following equation holds, and if the withstand voltage design and the type of semiconductor material are determined, the optimum carrier concentration is determined. . However, amorphous or polycrystalline semiconductors have difficulty controlling the carrier concentration. [Number 1] (wherein, ε s is the dielectric constant of the material, E c is the maximum dielectric breakdown electric field, q is the basic charge, BV is the withstand voltage as a design value, and N D is the carrier concentration). PRIOR ART DOCUMENT Patent Document Patent Document 1 :WO2015/025499A1 Non-Patent Document Non-Patent Document 1: "Fundamentals of Power Semiconductor Devices", B. Jayant Baliga, Springer Science & Business Media, 2010/04/02

本發明之目的在於,提供一種無需初始載子濃度控制之高耐壓且低電阻之半導體元件。 本發明者等人針對難以進行初始載子之濃度調整之問題進行努力研究,結果發現,只要半導體層與電極滿足特定之關係式,則根據與先前之單極功率器件相關之設計指南不同之動作原理,可不依賴於載子濃度而利用外因性載子,而獲得高耐壓且低電阻之半導體元件,從而完成了本發明。 根據本發明,提供以下之半導體元件等。 1.一種半導體元件,其特徵在於: 具有隔開之一對歐姆電極及肖特基電極、以及 與上述歐姆電極及上述肖特基電極相接之半導體層,且 滿足下述式(I)。 [數2](式中,n為上述半導體層之載子濃度(cm-3 ),ε為上述半導體層之介電常數(F/cm),Ve 為上述歐姆電極與上述肖特基電極之間之正向有效電壓(V),q為基本電荷(C),L為上述歐姆電極與上述肖特基電極之間之距離(cm)) 2.如1之半導體元件,其特徵在於:上述半導體層包含金屬氧化物。 3.如2之半導體元件,其特徵在於:上述金屬氧化物含有選自In、Zn、Ga、Sn及Al中之一種以上之元素。 4.如1至3中任一項之半導體元件,其特徵在於:上述肖特基電極包含選自Pd、Mo、Pt、Ir、Ru、W、Cr、Re、Te、Mn、Os、Fe、Rh、Co及Ni中之一種以上之金屬或其氧化物。 5.如1至4中任一項之半導體元件,其特徵在於:上述歐姆電極包含選自Ti、Mo、Ag、In、Al、W、Co及Ni中之一種以上之金屬或其化合物。 6.如1至5中任一項之半導體元件,其特徵在於:上述半導體層包含非晶或多晶。 7.如1至6中任一項之半導體元件,其特徵在於:上述半導體層之特性溫度為1500 K以下。 8.如1至7中任一項之半導體元件,其特徵在於:於自肖特基電極之外周部向歐姆電極面劃垂線時,上述歐姆電極面處於上述垂線之內側。 9.如1至8中任一項之半導體元件,其特徵在於:耐壓為0.5 MV/cm以上。 10.如1至9中任一項之半導體元件,其特徵在於:上述半導體層介於上述歐姆電極與上述肖特基電極之間。 11.如10之半導體元件,其特徵在於:進而具有導電性矽基板,且 上述歐姆電極或上述肖特基電極與上述導電性矽基板相接。 12.如1至9中任一項之半導體元件,其特徵在於:上述歐姆電極與上述肖特基電極隔開間隔地存在於上述半導體層之一表面上。 13.一種肖特基能障二極體,其特徵在於:使用如1至12中任一項之半導體元件。 14.一種接面電晶體,其特徵在於:使用如1至12中任一項之半導體元件。 15.一種電子電路,其特徵在於:使用如1至12中任一項之半導體元件、如13之肖特基能障二極體或如14之接面電晶體。 16.一種電氣機器、電子機器、車輛或動力機構,其特徵在於:使用如15之電子電路。 根據本發明,能夠提供一種無需初始載子濃度控制之高耐壓且低電阻之半導體元件。It is an object of the present invention to provide a semiconductor device having high withstand voltage and low resistance without initial carrier concentration control. The present inventors have made an effort to study the problem that it is difficult to adjust the concentration of the initial carrier, and as a result, it has been found that as long as the semiconductor layer and the electrode satisfy a specific relationship, the operation is different according to the design guidelines related to the previous unipolar power device. According to the principle, an exogenous carrier can be used without depending on the carrier concentration, and a semiconductor element having high withstand voltage and low resistance can be obtained, thereby completing the present invention. According to the present invention, the following semiconductor elements and the like are provided. A semiconductor device comprising: a pair of ohmic electrodes and a Schottky electrode; and a semiconductor layer in contact with the ohmic electrode and the Schottky electrode, and satisfying the following formula (I). [Number 2] (wherein n is a carrier concentration (cm -3 ) of the semiconductor layer, ε is a dielectric constant (F/cm) of the semiconductor layer, and Ve is a positive relationship between the ohmic electrode and the Schottky electrode To the effective voltage (V), q is the basic charge (C), and L is the distance (cm) between the ohmic electrode and the Schottky electrode. 2. The semiconductor device according to 1, wherein the semiconductor layer comprises Metal oxide. 3. The semiconductor device according to 2, wherein the metal oxide contains one or more elements selected from the group consisting of In, Zn, Ga, Sn, and Al. 4. The semiconductor device according to any one of 1 to 3, wherein the Schottky electrode comprises Pd, Mo, Pt, Ir, Ru, W, Cr, Re, Te, Mn, Os, Fe, One or more of Rh, Co and Ni or an oxide thereof. 5. The semiconductor device according to any one of 1 to 4, wherein the ohmic electrode comprises a metal selected from the group consisting of Ti, Mo, Ag, In, Al, W, Co, and Ni, or a compound thereof. 6. The semiconductor device according to any one of 1 to 5, wherein the semiconductor layer comprises amorphous or polycrystalline. 7. The semiconductor device according to any one of 1 to 6, wherein the semiconductor layer has a characteristic temperature of 1500 K or less. 8. The semiconductor device according to any one of 1 to 7, wherein the ohmic electrode surface is located inside the perpendicular line when the peripheral portion of the Schottky electrode is perpendicular to the ohmic electrode surface. 9. The semiconductor device according to any one of 1 to 8, characterized in that the withstand voltage is 0.5 MV/cm or more. 10. The semiconductor device according to any one of 1 to 9, wherein the semiconductor layer is interposed between the ohmic electrode and the Schottky electrode. 11. The semiconductor device according to 10, further comprising: a conductive germanium substrate, wherein the ohmic electrode or the Schottky electrode is in contact with the conductive germanium substrate. 12. The semiconductor device according to any one of 1 to 9, wherein the ohmic electrode is present on a surface of one of the semiconductor layers at a distance from the Schottky electrode. A Schottky barrier diode characterized by using the semiconductor device according to any one of 1 to 12. A junction transistor characterized by using the semiconductor element according to any one of 1 to 12. An electronic circuit characterized by using a semiconductor element according to any one of 1 to 12, such as a Schottky barrier diode of 13 or a junction transistor such as 14. 16. An electrical machine, an electronic machine, a vehicle or a power mechanism, characterized in that an electronic circuit such as 15 is used. According to the present invention, it is possible to provide a semiconductor element having high withstand voltage and low resistance without initial carrier concentration control.

本發明之半導體元件具有隔開之一對歐姆電極及肖特基電極、以及與歐姆電極及肖特基電極相接之半導體層,且滿足下述式(I)。 [數3](式中,n為上述半導體層之載子濃度(cm-3 ),ε為上述半導體層之介電常數(F/cm),Ve 為上述歐姆電極與上述肖特基電極之間之正向有效電壓(V),q為基本電荷(1.602×10-19 C),L為上述歐姆電極與上述肖特基電極之間之距離(cm)) n之下限可為0,但較佳為1×1010 以上。 更佳為滿足以下之式(I-1),進而較佳為滿足以下之式(I-2)。 [數4][數5]於上述式中,載子濃度係藉由CV(capacitance-voltage,電容-電壓)測定,且使用下述式而算出(參照APPLIED PHYSICS LETTERS,101,113505(2012))。 [數6]A:肖特基電極及歐姆電極重複之部分之面積(cm2 ) C:所測定出之電容值(F) εs :相對介電常數(-) ε0 :真空之介電常數(8.854×10-14 F/cm) Ndepl :載子濃度(cm-3 ) Vbi :內建電壓(V) k:玻耳茲曼常數(8.617×10-5 eV/K) T:測定時之試樣溫度(K) q:基本電荷(1.602×10-19 C) V:施加電壓(V) L可藉由實施例中揭示之方法求出。 Ve 如下所述般,可為0.1 V。 關於介電常數ε,只要確定半導體種類之組成及晶系,則可利用文獻值之相對介電常數,根據相對介電常數及真空之介電常數之乘積而確定。又,於文獻中之報告例較少或根據報告例不同差異較大之情形時,亦可進行實際測定。於進行實際測定之情形時,可利用如下方法算出,即,根據CV測定之膜厚依存性,測定3點以上之膜厚(L)之電容值,若於縱軸對C/A進行繪圖,於橫軸對1/L進行繪圖,則其斜率成為介電常數ε。 為了使半導體元件滿足式(I),降低半導體層中之載子濃度。具體而言,降低半導體中之摻雜劑濃度。例如,於如氧化物半導體般,存在於半導體中之氫原子或氧缺陷作為摻雜劑發揮功能之半導體之情形時,形成缺陷較少且膜密度較高之膜對降低載子濃度有效。 圖1係本發明之一實施形態之半導體元件之概略剖視圖。 該半導體元件1(立式)依序具有肖特基電極10、半導體層30、歐姆電極20。進而,於肖特基電極10之與半導體層30側為相反之側具有導電性基板40。 圖2係本發明之其他實施形態之半導體元件之概略剖視圖。 該半導體元件2(立式)依序具有肖特基電極10、半導體層30、歐姆電極20。進而,於歐姆電極20之與半導體層30側為相反之側具有導電性基板40。又,歐姆電極20之兩側具有絕緣層50,以歐姆電極20與兩側之絕緣層50形成1層。圖3之半導體元件3與圖2之元件2僅歐姆電極20之寬度較寬這一情況不同。 圖4係作為本發明之其他實施形態之半導體元件之概略立體圖。 該半導體元件4(橫置式)於半導體層30之對向之第1及第2面中之第1面之上,肖特基電極10與歐姆電極20隔開間隔地配置。進而,於半導體層30之第2面上具有絕緣性基板60。 於滿足上述式(I)之本發明之半導體元件中,半導體層之初始載子濃度較小,外因性載子作為導電之主因子發揮功能。半導體層之阱密度較小,不妨礙外因性載子之傳導。 再者,於專利文獻1中,存在下述式之關係,基於先前之單極功率器件之載子濃度設計指南,於載子濃度之控制性上存在問題。 [數7](式中,n、ε、Ve 、q及L與式(I)相同) 本發明之半導體元件之反向漏電流較小,正向導通電阻較低,可提取大電流。又,即便使用廉價之矽基板或金屬基板作為導電性基板,亦表現出良好之整流特性。進而,即便以濺鍍等生產性優異之方式對氧化物半導體層製膜,亦表現出良好之整流特性。本發明之半導體元件尤其於立式肖特基能障二極體用途中優異。 <關於式(I)> 通常於不存在載子之絕緣體中,下述式(1)成立。 Jins =(9/8)με(V2 /L3 ) (1) Jins :電流密度(A/cm2 ) μ:遷移率(cm2 /V·s) ε:物質之介電常數(F/cm) V:施加電壓(V) L:電流流經之區域之厚度(cm)。 另一方面,關於存在載子之導電體,下述式(2)成立。 Johm =qnμ(V/L)  (2) Johm :電流密度(A/cm2 ) q:基本電荷(1.602×10-19 C) n:載子濃度(cm-3 ) μ:遷移率(cm2 /V·s) V:施加電壓(V) L:電流流經之區域之厚度(cm)。 於Jins =Johm 之條件下,下述式(3)成立。 [數8](式中,n、ε、V、q及L與式(1)、(2)相同) 因此,於下述式(4)成立之情形時,意指Jins >Johm ,絕緣性傳導之作用較大。即,意指外因性載子作為導電之主因子發揮功能。 [數9](式中,n、ε、V、q及L與式(1)、(2)相同) 於以單極表示整流特性之肖特基能障二極體、接面場效電晶體(JFET)、金屬氧化膜半導體場效電晶體(MOSFET)中存在漂移區域,通常,於漂移區域中,上述式(2)之關係成立。於此情形時,施加電壓V意指施加於漂移層之電壓。於上述式(I)中,將Ve 定義為正向有效電壓,但其係指如下電壓,即,於考慮到實際之器件構成之情形時,相對於施加電壓V,去除了用於解除能帶彎曲之內建電壓Vbi 等之作用後之對漂移層之有效電壓。 於肖特基能障二極體、接面場效電晶體(JFET)、金屬氧化膜半導體場效電晶體(MOSFET)等器件中,在半導體層器件之間具有一對歐姆電極及肖特基電極,只要上述式(I)成立,則外因性載子作為電氣傳導之主因子發揮功能。 介電常數ε係半導體之相對介電常數εr 與真空之介電常數ε0 (8.854×10-14 (8.854E-14)[F/cm])之乘積。εr 根據材料不同而為不同參數,但較佳為3~20,更佳為5~16,進而較佳為9~13。若相對介電常數過低,則有外因性載子之注入變少而無法獲得高電流之虞。若相對介電常數過大,則有寄生電容之增加或電流特性產生遲滯之虞。 關於正向有效電壓Ve ,若考慮到實際之正向特性使用時對單極器件之施加電壓通常為0.5 V~1.5 V左右,且內建電壓Vbi 通常為0.7~1.3 V左右,則可將Ve 視為0.1 V左右。基本電荷之值為1.602×10-19 C/個,故若將εr 假設為10,則鑒於式(I),載子濃度n之上限值係藉由半導體層之一對歐姆電極及肖特基電極之間隔L而確定,如表1所示。 [表1] L較佳為10 nm<L<100000 nm,更佳為20 nm<L<10000 nm,進而較佳為30 nm<L<1000 nm,最佳為50 nm<L<300 nm。若電極間間隔L過短,則有於耐壓之觀點上產生問題之虞,若L過大,則有電流值降低或於立式元件中半導體層之膜厚增加而導致成膜費時之虞。 L與n較佳為滿足下述式(I-a)所示之關係,更佳為滿足下述式(I-b)所示之關係,進而較佳為滿足下述式(I-c)所示之關係,特佳為滿足下述式(I-d)所示之關係。 [數10](式中,n、ε、Ve 、q及L與式(I)相同) 若n過低,則有存在於半導體層內部之阱產生影響而擴散電流之作用變大,電流特性變差之虞。另一方面,若n成為式(I)之εVe /qL2 以上,則漂移電流之作用變大,接近先前之動作特性而難以產生本發明之效果。 <半導體元件之耐壓> 本發明之半導體元件於半導體層之間具有一對歐姆電極及肖特基電極。與先前之功率器件相比,因設計載子濃度變低,故耐壓VBD 之設計相對於VBD ~Ec L/2而成為VBD ~Ec L,可期待以相同L進行對比,提高2倍左右之耐壓。於此,Ec 為最大絕緣破壞電場,L為電極間長度。 又,於先前之功率器件中,由於初始載子濃度較高,故於施加逆向偏壓時之漏電流較大,於自肖特基電極之外周部(側面)向歐姆電極面劃垂線時,難以取得歐姆電極面內包於來自肖特基面之垂線般之元件構成。於本發明中,半導體層中之初始載子濃度較低,於施加正向電壓時,外因性載子僅注入在自肖特基電極之外周部向歐姆電極面劃垂線時,歐姆電極面內包於來自肖特基面之垂線之範圍內。另一方面,於施加逆向偏壓時,遍及半導體層之整體不存在載子,故因迴繞所致之漏電流之影響較小。 圖5係用於說明圖2之半導體元件之電極面之圖。於圖5中,肖特基電極之外周部係以符號12所示之部分,歐姆電極面係以符號22所示之部分。自肖特基電極之外周部12向歐姆電極面22所劃之垂線以符號A表示。 於立式之功率器件中,通常,半導體層下部為歐姆電極,但於歐姆電極處於自肖特基電極所劃之垂線之內側時,能夠容易地將肖特基電極用於半導體層下部。又,已知於通常之功率器件中使用保護環等電場緩和構造以實現逆向漏電流之減少,藉由此種之構成,可省略或削減成為製程缺點之該等電場緩和構造。 於外因性載子成為支配之單極之功率器件中,如上文所述般耐壓成為VBD ~Ec L,故根據電極間長度L與耐壓VBD 之測定結果可容易地確定絕緣破壞電場。於此,單位L之耐壓相當於絕緣破壞電場。若單位膜厚之耐壓較高,則於設計相同耐壓元件時可減小L,故外因性載子之注入增加,而能夠提供更低電阻之元件。關於單位L之耐壓,較佳為0.5 MV/cm以上,更佳為0.8 MV/cm以上,進而較佳為1.0 MV/cm以上,特佳為3.0 MV/cm以上。單位L之耐壓可藉由測定崩潰電壓(V),並除以L之長度而求出。例如,於肖特基能障二極體之情形時,在掃引逆向電壓之情形時,將已達到1×10-3 A之電流值之最初之電壓值定義為崩潰電壓。 又,單位L之耐壓可根據半導體層之材料選擇進行調整。於本發明中,在半導體層之材料為帶隙1 eV以上且包含非晶或多晶之半導體層時,可達到0.5 MV/cm以上。於為帶隙2 eV以上之材料時,達到1.0 MV/cm以上,於為帶隙2 eV以上且包含非晶或多晶之半導體層時,可達到3.0 MV/cm以上。 <特性溫度> 特性溫度係表示非晶或多晶體所特有之傳導帶下端之帶尾能階之特徵的參數,關於在傳導帶下端具有帶尾能階之外因性載子成為支配之半導體,遵循下述式(5)之特性。 [數11]J:電流密度(A/cm2 ) u:遷移率(cm2 /V·s) Nc :半導體之有效狀態密度(cm-3 ) Nt :傳導帶下端部之帶尾能階密度(cm-3 ) ε:物質之介電常數(F/cm) V:施加電壓(V) L:電流流經之區域之厚度(cm) e:基本電荷(1.602×10-19 C) I:Tc/T Tc:特性溫度(K) T:實際溫度(K) 特性溫度Tc係成為Tc>T之參數,於帶尾能階數較多,妨礙藉由阱而注入之外因性載子之傳導之情形時,成為較大之值。實施電流-電壓測定,根據式(5)可知,Log(J)-Log(V)之曲線之斜率為I+1,因此,根據斜率求出I,並算出Tc。但是,Tc之值相對於某連續之範圍之施加電壓成為固定之情形成為半導體層具有帶尾能階之指標。較佳為Tc<1500 K,更佳為Tc<900 K,進而較佳為Tc<600 K。若Tc之值較大,則有帶尾能階所捕獲之外因性載子數增加,器件特性高電阻化之虞。 特性溫度可藉由實施電流-電壓測定,根據Log(J)-Log(V)之曲線之斜率而求出。特性溫度可藉由於非晶或多晶半導體中提高原子結構之短距離秩序性而降低。例如,於非晶金屬氧化物半導體之情形時,密度較低之膜有短距離秩序性變低,特性溫度變高之傾向。可確認於藉由濺鍍成膜之非晶金屬氧化物半導體中,密度與成膜條件存在關係。靶-基板距離越近,濺鍍壓力越低,成膜時之基板溫度越高或成膜後之退火溫度越高,或濺鍍成膜時之施加於靶之施加電壓越高,越易於形成高密度之膜。又,於濺鍍成膜時若添加0.1~10體積%之H2 或H2 O作為濺鍍氣體,則易於獲得高密度之膜。若為非晶或多晶半導體層含有選自In、Zn、Ga及Sn中之一種以上之元素之金屬氧化物半導體,則可利用對象性較高之s軌道,故不易受到週期電位之混亂之影響,特性溫度易於變低。 <漂移層之積層化(限定於立式之元件)> 可獲得如下之半導體元件(立式),即,具有以成為下述式(6)之載子濃度nL 較低之半導體層(L1 、L2 、…Ln )(nL 及Ln 表示自肖特基電極向歐姆電極計數時,位於第n號之載子濃度較低之層的載子濃度及膜厚)與載子濃度nh 較高之半導體層(d1 、d2 、…dn-1 )(nh 及dn 表示自肖特基電極向歐姆電極計數時,位於第n號之載子濃度較高之層的載子濃度及膜厚)於漂移層上重複之構造。 [數12](式中,nL 表示自肖特基電極向歐姆電極計數時位於第n號之載子濃度之較低之層的載子濃度,ε表示第n號之載子濃度較低之半導體層之介電常數,Ve 表示施加於第n號之載子濃度較低之半導體層之有效電壓(可設為Ve =0.1 V),q表示基本電荷,Ln 表示第n號之載子濃度較低之半導體層之膜厚) 較單層之漂移構成而言藉由進行積層而可期待耐壓之提高及電阻值之減少。於此情形時,Ln 較佳為10 nm<Ln <1000 nm,更佳為20 nm<Ln <300 nm,進而較佳為30 nm<Ln <200 nm,特佳為30 nm<Ln <100 nm。有若Ln 過短則差異變大,若Ln 過長則電阻值變高之虞。又,dn 較佳為3 nm<dn <30 nm,更佳為5 nm<dn <10 nm。若dn 過長,則有施加逆向偏壓時空乏層未擴展至自肖特基電極至歐姆電極之全域而於耐壓之觀點上產生問題之虞。若dn 過短,則有未發揮作為Ln 與Ln 1 之間隔層之作用而未作為積層構成發揮功能之虞。nh 較佳為下述式(6-a),更佳為下述式(6-b),進而較佳為下述式(6-c)。 [數13](式中,ε表示第n號之載子濃度較高之半導體層之介電常數,Ve 表示施加於第n號之載子濃度較高之半導體層之有效電壓(可設為Ve =0.1V),q表示基本電荷,dn 表示第n號之載子濃度較高之半導體層之膜厚) 若nh 過大,則有於載子濃度較高之半導體層抑制施加逆向偏壓時空乏層之延伸而難以維持耐壓之虞。若nh 過小,則有於正向施加時亦需要向載子濃度較高之層注入外因性載子,結果,複數個載子濃度較低之半導體層作為一個載子濃度較低之層工作而電阻值增高之虞。 與肖特基電極相接者較佳為載子濃度較低之層。 <半導體元件之串聯連結> 於先前之單極功率器件之耐壓設計中,在施加額定耐壓之電壓時,肖特基金屬側之半導體界面之電場強度達到絕緣破壞電場附近,難以進行半導體元件之連結。例如,於肖特基能障二極體之情形時,即便將600 V耐壓之元件複數個串聯,亦難以獲得600 V以上之耐壓。於本發明之初始載子濃度較低且使用外部注入載子之半導體元件(功率器件)中,在複數個串聯連接之情形時,相應於所連結之個數,耐壓以額定耐壓之乘積而增加。因此,能夠容易地提供所需之耐壓之元件。 <半導體元件之構成層> (1)半導體層 半導體層並無特別限定,較佳為包含多晶或非晶。又,較佳為包含金屬氧化物半導體,更佳為包含含有選自In、Zn、Ga、Sn及Al中之一種以上之元素之金屬氧化物半導體。若為非晶,則大面積均勻性優異,對施加逆向偏壓時之衝擊離子化降低且耐壓提高有效。若為多晶,則大面積均勻性且傳導特性較佳。由金屬氧化物半導體製造半導體層時,可採用使用燒結體濺鍍靶之大面積性優異之成膜方法。藉由將含有選自In、Zn、Ga、Sn及Al中之一種以上之元素之金屬氧化物半導體利用於半導體層,而可利用金屬元素之s軌道之傳導特性,故即便為非晶、多晶,亦形成軌道重疊且傳導特性優異之半導體層。 金屬氧化物半導體可包含1種或2種以上之金屬氧化物。作為金屬氧化物,可列舉In、Sn、Ge、Ti、Zn、Y、Sm、Ce、Nd、Ga或Al之氧化物等。較理想為包含選自In、Zn、Ga及Sn中之一種以上之元素。 金屬氧化物半導體之金屬本質上可包含選自In、Sn、Ge、Ti、Zn、Y、Sm、Ce、Nd、Ga及Al中之一種以上。又,金屬之例如95原子%以上、98原子%以上、或99原子%以上亦可為選自In、Sn、Ge、Ti、Zn、Y、Sm、Ce、Nd、Ga或Al中之一種以上。 構成金屬氧化物半導體之金屬氧化物較佳為滿足下述式(A)~(C)之原子比。若為此種組成,則可設為高耐壓、低導通電阻。 0≦x/(x+y+z)≦0.8     (A) 0≦y/(x+y+z)≦0.8     (B) 0≦z/(x+y+z)≦1.0     (C) (式中,x表示選自In、Sn、Ge及Ti中之一種以上之元素之原子數, y表示選自Zn、Y、Sm、Ce及Nd中之一種以上之元素之原子數, z表示選自Ga及Al中之一種以上之原子數) 若x超過0.8,則於x為In或Sn之情形時,有金屬氧化物之絕緣性變低,而不易獲得肖特基接合之虞,且於x為Ge或Ti之情形時,有金屬氧化物之絕緣性變高,而成為因歐姆損失所致之發熱之原因之虞。 更佳為上述組成(A)~(C)分別為下述式(A-1)~(C-1)。 0≦x/(x+y+z)≦0.7     (A-1) 0≦y/(x+y+z)≦0.8     (B-1) z為Ga時:0.02≦z/(x+y+z)≦1.0 z為Al時:0.005≦z/(x+y+z)≦0.5     (C-1) (式中,x、y及z與上述式(A)~(C)相同) z為Ga時,若低於0.02,則有金屬氧化物中之氧容易脫離,電氣特性不均之虞。 進而較佳為上述組成(A)~(C)分別為下述式(A-2)~(C-2)。 0.1≦x/(x+y+z)≦0.5  (A-2) 0.1≦y/(x+y+z)≦0.5  (B-2) 0.03≦z/(x+y+z)≦0.5 (C-2) (式中,x及y與上述式(A)~(C)相同,z為Ga) 又,上述組成(A)及(C)較佳為分別為下述式(A-3)及(C-3)。 0≦x/(x+y+z)≦0.25   (A-3) 0.3≦z/(x+y+z)≦1.0  (C-3) (式中,x、y及z與上述式(A)、(C)相同) 構成金屬氧化物半導體層之金屬氧化物可為非晶質亦可為晶質,結晶可為微晶亦可為單晶。較佳為金屬氧化物為非晶質或微晶。於將金屬氧化物設為單晶時,使用以晶種為起點使結晶生長、或MBE(分子束磊晶)或PLD(脈衝雷射沈積)等方法。若於SiO2 表面或金屬表面上結晶生長,則容易產生結晶缺陷,於用作在縱向上通電之器件時,有該結晶缺陷導致不良狀況之虞。於在SiO2 表面或金屬表面上結晶生長之情形時,以粒徑不會變得過大之方式,適當地調整加熱溫度、時間等。 另一方面,於非晶質之情形時,即便存在有懸鍵,由於未作為結晶缺陷而存在,故亦可緩和電氣特性之不均或大幅度之特性劣化。進而,金屬氧化物與Si半導體等之共價鍵不同而離子鍵結性較強,故藉由懸鍵而成之能階接近導電帶或充滿體。因此,金屬氧化物與Si或SiC等相比,因構造所致之遷移率等電氣特性之差較小。若積極地利用金屬氧化物之此種性質,則即便為單晶,亦能夠以較高之良率提供高耐壓且可靠性較高之大電流二極體或開關元件。 於此,所謂「非晶質」係指取得金屬氧化物層之膜厚方向之剖面,於藉由穿透式電子顯微鏡等之電子束繞射方法進行評價之情形時,無法獲得明顯之繞射光點者。較理想為自電子束之照射區域10 nm左右之較寬之區域取得繞射像。所謂明顯之光點係指自繞射像觀察到具有對稱性之繞射點。 又,「非晶質」亦包含具有局部結晶化或微晶化之部分之情形。若將電子束照射至局部結晶化之部分,則有可確認到繞射像之情形。 所謂「微晶結構」係指結晶粒徑之尺寸為次微米以下,且不存在明確之晶界者。 所謂「多晶」係指結晶粒徑之尺寸超過微米尺寸,且存在明確之晶界者。 構成金屬氧化物半導體層之各層之載子濃度通常為1×1011 ~1×1018 cm-3 ,例如為1×1013 ~1×1018 cm-3 。載子濃度例如可藉由CV測定而求出。 二極體所需之性質有高速切換、高耐壓、低導通電阻,只要使用利用金屬氧化物之半導體元件,則可兼具該等特性。其原因在於,金屬氧化物之帶隙原本較寬,且為高耐壓。又,藉由氧缺陷易於成為n型而不易形成p型,此情形亦有利於高速切換。 為了降低導通電阻,只要使之結晶化以提高遷移率即可,但較佳為限於無法形成晶界之程度。晶界中經常會存在孔隙,有形成電場時產生極化,該極化使耐壓性能降低之虞。於耐壓之降低顯著之情形時,較佳為直接以非晶質之形式使用。於作為非晶質而使用之情形時,雖然亦取決於形成金屬氧化物層之元素之種類,但只要將加熱處理條件設定為例如500℃以下且1小時以內即可。藉由以500℃以下之低溫進行加熱,能夠獲得穩定之非晶質狀態。 半導體層之膜厚並無限定,通常為100~8000 nm。 (2)肖特基電極 構成肖特基電極之金屬並無特別限定,較佳為選自Pd、Mo、Pt、Ir、Ru、Ni、W、Cr、Re、Te、Mn、Os、Fe、Rh及Co中之一種以上之金屬(包含合金)或該金屬之氧化物,更佳為選自Pd、Pt、Ir及Ru中之一種以上之金屬(包含合金)或該金屬之氧化物。 又,較佳為與上述氧化物半導體層之耐壓層形成良好之肖特基接觸之金屬或金屬氧化物。更佳為,於與氧化物半導體之組合中,形成較高之肖特基障壁之Pd氧化物、Pt氧化物、Ir氧化物、Ru氧化物。 該等氧化物通常有藉由氧化之狀態而形成半導體或絕緣體之情形,但可藉由選擇組成或製膜條件而維持高載子密度之金屬狀態,且藉由與氧化物半導體之接觸而形成良好之肖特基接觸。為使氧化物形成良好之肖特基電極,較佳為,肖特基電極之載子濃度理想為1018 cm-3 以上。若未達1018 cm-3 ,則有與氧化物半導體層之接觸成為p-n接合,有損高速響應等肖特基二極體之優點之情形。載子濃度例如可藉由霍爾測定等求出。 作為用於獲得金屬氧化物層之製造方法,並無特別限定,可較佳地使用於含氧環境下,進行該金屬靶之反應性濺鍍之方法。 肖特基電極之厚度通常為2 nm~500 nm,較佳為5 nm~200 nm。若過薄,則有受到所接觸之金屬之影響而使正向偏壓時之導通電阻增加之虞。若過厚,則有由於自身之電阻,仍導致正向偏壓時之導通電阻增加,或肖特基界面之平坦性變差、耐壓性降低之虞。 關於肖特基電極,為了降低與基板或電流提取電極之接觸電阻及提高密接性,可於與半導體層相接之側之相反側,積層包含複數個組成不同之金屬或金屬氧化物之層。 (3)歐姆電極 歐姆電極之材料只要為能夠與半導體層進行良好之歐姆連接,則並無特別限定,較佳為選自Ti、Mo、Ag、In、Al、W、Co及Ni中之一種以上之金屬(包含合金)或其化合物(氧化物等),更佳為選自Mo、Ti、Au、Ag及Al中之一種以上之金屬(包含合金)或其化合物。又,亦可藉由複數個層構成歐姆電極。例如,於與半導體層相接之側使用Mo電極層,為了提取大電流,進而較厚地積層Au或Al等金屬層,該層可作為打線接合之基礎。 歐姆電極之厚度通常為10 nm~5 μm。 (4)製膜方法 各層之製膜方法並無特別限定,可使用如下方法,即,熱CVD(chemical vapor deposition,化學氣相沈積)法、CAT-CVD(catalytic chemical vapor deposition,催化化學氣相沈積)法、光CVD法、霧化CVD法、MO-CVD(Metal-organic Chemical Vapor Deposition,金屬有機化合物化學氣相沈積)法、電漿CVD法等CVD法;MBE(Molecular Beam Epitaxy,分子束磊晶法)、ALD(atomic layer deposition,原子層沈積法)等原子等級控制之製膜方法;離子鍍覆、離子束濺鍍、磁控濺鍍等PVD(Physical Vapor Deposition,物理氣相沈積)法;刮刀法、射出法、擠壓法、熱加壓法、溶膠凝膠法、氣溶膠沈積法等先前公知之使用陶瓷步驟之方法;塗佈法、旋轉塗佈法、印刷法、噴霧法、電鍍法、鍍覆法、膠束電解法等濕式法等。 於選擇金屬氧化物半導體之情形時,半導體層之成膜方法較佳為濺鍍。成膜氣體較佳為自稀有氣體、氧氣、氫氣、水中選擇至少1種以上。濺鍍靶與基板距離(TS間隔)較佳為10 mm~200 mm。若TS間隔過短,則有無法放電之虞。於TS間隔過長之情形時,半導體之膜質變得稀疏,有可能成為特性溫度較大之膜。 (5)基板 半導體元件之基板並無特別限定,可使用公知者。作為基板,可列舉導電性基板、半導體基板、絕緣性基板等。 於立式半導體元件中,如圖1,2所示般,可使用導電性基板。導電性基板可與肖特基電極或歐姆電極接觸而配置。作為導電性基板,可使用矽單晶基板、矽多晶基板、矽結晶基板等先前公知之表面平滑性優異之基板。又,除矽基板以外亦可使用SiC基板、GaN基板、GaAs基板等半導體基板。亦可利用Al基板、Cu基板、Ni基板等導電性優異之金屬基板。若考慮到量產性及成本,則較佳為矽基板。矽基板根據摻雜之有無及種類而存在n型、i型、p型,於縱向上流動電流時,較佳為電阻較小之n型或p型。作為摻雜劑,可使用先前公知之B、P、Sb等。尤其於欲降低電阻之情形時,亦可使用As或紅磷作為摻雜劑。 於橫置式半導體元件中,如圖4所示般,可使用絕緣性基板。絕緣性基板可與半導體層接觸而配置。作為絕緣性基板,只要為具有絕緣性者,則並無特別限制,可於不喪失本發明之效果之範圍內任意地選擇通常所使用者。例如,除石英玻璃、鋇硼矽酸鹽玻璃、鋁硼矽酸鹽玻璃、鋁矽酸鹽玻璃等以熔融法或浮式法所製作之無鹼玻璃基板、陶瓷基板以外,可使用具有可耐受本製作步驟之處理溫度之耐熱性之塑料基板等。 又,亦可使用介電基板作為絕緣性基板。 作為介電基板,可列舉鈮酸鋰基板、鉭酸鋰基板、氧化鋅基板、水晶基板、藍寶石基板等。 又,可使用於不鏽鋼合金等之金屬基板之表面設有絕緣膜或介電膜之基板。又,亦可於基板形成絕緣膜作為基底膜。作為基底膜,可使用CVD法或濺鍍法等,形成氧化矽膜、氮化矽膜、氮氧化矽膜、或氧氮化矽膜等之單層或積層。 關於半導體基板,只要保持表面之平滑性,則材料並無特別限定。 作為半導體基板,可列舉:將載子濃度調整至1×1018 cm-3 以下之Si基板、GaN基板、SiC基板、GaP基板、GaAs基板、ZnO基板、Ga2 O3 基板、GaSb基板、InP基板、InAs基板、InSb基板、ZnS基板、ZnTe基板、金剛石基板等。 半導體基板可為單晶亦可為多晶。又,亦可為部分地含有非晶質基板或非晶質之基板。亦可使用於導電體基板、半導體基板、絕緣性基板上,利用CVD(化學氣相沈積)等方法形成有半導體膜之基板。 作為基板,亦可使用於上述導電性基板、半導體基板或絕緣性基板上,具有由複數個材料構成之任意構造、層構造、電路、配線、電極等之基材。 作為任意構造之材料,例如可列舉形成大規模積體電路(LSI)上之後段製程之金屬、層間絕緣膜等各種金屬或絕緣物之複合材料。 作為層構造之層,並無特別限定,可使用電極層、絕緣層、半導體層、介電層、保護膜層、應力緩衝層、遮光層、電子/電洞注入層、電子/電洞傳輸層、發光層、電子/電洞阻擋層、結晶生長層、密接性提高層、記憶體層液晶層、電容器層、蓄電層等公知之層。 作為電極層,通常可列舉:Al層、Si層、Sc層、Ti層、V層、Cr層、Ni層、Cu層、Zn層、Ga層、Ge層、Y層、Zr層、Nb層、Mo層、Tc層、Ru層、Rh層、Pd層、Ag層、Cd層、In層、Sn層、Sb層、Te層、Hf層、Ta層、W層、Re層、Os層、Ir層、Pt層、Au層、含有該等層之金屬一種以上之合金層、及氧化物電極層等。亦可增加氧化物半導體或Si等半導體之載子濃度,用於電極層。 作為絕緣層,通常可列舉:包含選自由Al、Si、Sc、Ti、V、Cr、Ni、Cu、Zn、Ga、Ge、Y、Zr、Nb、Mo、Tc、Ru、Rh、Pd、Ag、Cd、In、Sn、Sb、Te、Hf、Ta、W、Re、Os、Ir、Pt及Au所組成之群中之一種以上之金屬的氧化物絕緣膜、氮化膜等。 作為半導體層,不限單晶、多晶、非晶之結晶狀態而可廣泛地列舉Si層、GaN層、SiC層、GaP層、GaAs層、GaSb層、InP層、InAs層、InSb層、ZnS層、ZnTe層、金剛石層、Ga2 O3 、ZnO、InGaZnO等氧化物半導體層、稠五苯等有機半導體層等。 作為介電層,可列舉:鈮酸鋰層、鉭酸鋰層、氧化鋅層、水晶基板層、藍寶石層、BaTiO3 層、Pb(Zr,Ti)O3 (PZT)層、(Pb,La)(Zr,Ti)O3 (PLZT)層、Pb(Zr,Ti,Nb)O3 (PZTN)層、Pb(Ni,Nb)O3 -PbTiO3 (PNN-PT)層、Pb(Ni,Nb)O3 -PbZnO3 (PNN-PZ)層、Pb(Mg,Nb)O3 -PbTiO3 (PMN-PT)層、SrBi2 Ta2 O9 (SBT)層、(K,Na)TaO3 層、(K,Na)NbO3 層、BiFeO3 層、Bi(Nd,La)TiOx 層(x=2.5~3.0)、HfSiO(N)層、HfO2 -Al2 O3 層、La2 O3 層、La2 O3 -Al2 O3 層等。 作為保護膜層之膜,不論無機物或有機物,可列舉絕緣性均優異且水等之透過性較低之膜。作為保護膜層,例如可列舉:SiO2 層、SiNx 層(x=1.20~1.33)、SiON層、Al2 O3 層等。 作為應力緩衝層,可列舉AlGaN層等。 作為遮光層,例如可列舉包含金屬、金屬-有機物等之黑矩陣層、彩色濾光片層。 作為電子/電洞注入層,可列舉氧化物半導體層、有機半導體層等。 作為電子/電洞傳輸層,可列舉氧化物半導體層、有機半導體層等。 作為發光層,可列舉無機半導體層、有機半導體層等。 作為電子/電洞阻擋層,可列舉氧化物半導體層等。 作為基材,可列舉發電器件、發光器件、感測器、電力轉換器件、運算器件、保護器件、光電子器件、顯示器、記憶體、具有後段製程之半導體器件、蓄電器件等。 層構造之層可為單層亦可為2層以上之層。 本發明之半導體元件可用作功率半導體元件、(整流)二極體元件、肖特基能障二極體元件、靜電放電(ESD)保護二極體、暫態電壓保護(TVS)保護二極體、發光二極體、金屬半導體場效電晶體(MESFET)、接面場效電晶體(JFET)、金屬氧化膜半導體場效電晶體(MOSFET)、肖特基源極/汲極MOSFET(Metal-Oxide-Semiconductor Field Effect Transistor,金屬氧化物半導體場效應電晶體)、雪崩倍增型光電轉換元件、固體拍攝元件、太陽電池元件、光感測器元件、顯示元件、電阻變化記憶體等。由於可提取大電流,故亦尤其適用於功率用途。使用該元件之電子電路可應用於電氣機器、電子機器、車輛、動力機構等。 實施例 實施例1 將電阻率0.001 Ω·cm之n型Si基板(直徑4英吋、厚度250 μm)安裝於濺鍍裝置(CANON ANELVA製造:E-200S),成膜以下之積層電極。但是對於基板背面,為了消除測定時與探針儀之接觸電阻,而進行Ti 100 nm/Au 50 nm處理。首先使Ti於DC(Direct Current,直流)50 W、Ar環境下成膜15 nm,其次使Pd於DC50 W、Ar環境下成膜50 nm,最後,作為肖特基電極,於DC50 W、Ar與O2 之混合氣體環境下成膜20 nm之PdO。 繼而,將該基板與半導體用區域遮罩一起放置於濺鍍裝置(ULVAC製造:CS-200),成膜200 nm之InGaZnO(In:Ga:Zn(原子比)=1:1:1,於下文中將該組成之氧化物記為「InGaZnO(1:1:1)」,關於其他複合氧化物,亦同樣地記載除氧以外之原子比)作為耐壓層(半導體層)。成膜條件設為:DC300 W、Ar與H2 O之混合氣體環境(H2 O濃度:1體積%)。濺鍍靶-基板間距離(TS間隔)設為80 mm。取出該基板,使用電氣爐於空氣中300℃之條件下退火1小時。再次將該基板與電極用區域遮罩(孔直徑50 μm)一起放置於濺鍍裝置之後,成膜150 nm之Mo作為歐姆電極(直徑50 μm)。之後,使用相同遮罩成膜2 μm之Al電極。成膜條件均設為DC100 W、Ar環境。作為最終處理,實施200℃1小時之大氣下熟化處理。 再者,元件構成成為具有如下特徵之構成,即,如圖1所示般,於半導體層下部具有肖特基電極,自肖特基電極之外周部向歐姆電極面劃垂線時,歐姆電極面處於上述垂線之內側。 <電極間距離L> 電極間距離L係藉由剖面TEM(穿透式電子顯微鏡)像及剖面TEM之EDX(能量分散型X射線光譜法)像而取得。假設將包含InGaZnO之層設為半導體層,將肖特基電極設為PdO層,將歐姆電極設為Mo,將TEM剖面像之對比度基於EDX而與包含InGaZnO之層一致之部位設為半導體層並定義為電極間距離L。又,上述半導體層藉由EDX被Pd與Mo所夾持,且電極間距離L為200 nm。 利用半導體層經逆向偏壓而耗盡,經正向偏壓化而作為電阻層發揮作用這一情況,藉由CV(容量-電壓)測定而確認應該作為半導體發揮作用之厚度於上述L中並無問題。根據施加逆向電壓時之最小之容量值Cmin 及施加正向電壓時之最大之容量值Cmax ,使用C/A=εr ×ε0 /d之關係式求出Cmin 所對應之膜厚dmin 及Cmax 所對應之膜厚dmax ,其差量相對於L收斂於L±50%之值,故驗證了電極間距離L為200 nm。但是,本成膜方法之InGaZnO(1:1:1)之相對介電常數根據膜厚測定確認為16,故使用εr =16。通常報告有InGaZnO之相對介電常數為10~19左右之值。 C:容量值(F) A:電極之有效面積(cm2 ) d:作為半導體發揮作用之膜厚(cm) εr :相對介電常數 ε0 :真空之介電常數,8.854E-14[F/cm] 於此,電極之有效面積A表示隔開之一對歐姆電極及肖特基電極中,相對於半導體層相互內包之面積。關於本實施例,可將直徑50 μm之歐姆電極之面積視作A。 再者,於CV測定時,使用下述B1505之CMU(Capacitance Measure Unit,電容測量單元)單元,藉由偏壓T將電壓重疊而實施測定。測定頻率使用1 kHz,且AC振幅設為0.03 V。 <電極種類之鑑定> 電極種類之鑑定係於上述半導體層之鑑定之後,將夾住半導體層材料之電極種類視作歐姆電極及肖特基電極而實施。藉由剖面EDX像,推定包含Mo及Pd之金屬或金屬化合物為歐姆電極或肖特基電極。根據整流特性之確認,判斷Mo側為歐姆、Pd側為肖特基之電極種類。進而,藉由深度方向XPS(X-ray photoelectron spectroscopy,X射線光電子光譜法),一面對元件向深度方法進行Ar濺鍍,一面確認XPS光譜。自Mo側向Mo/InGaZnO界面,XPS之Mo光譜中之來自氧之峰值伴隨著InGaZnO所包含之氧濃度平緩地增加,且在遠離InGaZnO之Mo層上著眼於Mo之XPS光譜之9成以上可歸屬於純Mo,故歐姆電極設為Mo。 另一方面,成為如下狀態,即,於InGaZnO/PdO界面上自InGaZnO側向Pd,XPS之Pd光譜中之來自氧之峰值未伴隨InGaZnO所包含之氧濃度平緩地減少,某一定程度之氧包含於Pd中。又,於藉由EDX像觀察到Pd之區域中,明確地看到TEM像之對比度,且於深度方向XPS在純Pd之區域與InGaZnO之區域之間,存在有包含20 nm之電子密度少於純Pd之Pd之區域。由此,肖特基電極設為包含20 nm左右之Pd或PdO之層。如表2-1所示般,記為Pd(PdO)。 <結晶性之評價> 於觀察半導體層之剖面TEM時藉由電子束繞射方法,進行結晶性之評價。自電子束之照射區域為直徑10 nm以上之區域取得繞射像。於與膜厚方向及剖面平行之方向之複數個點中,繞射像中無法確認到光點形狀,故判斷半導體層為非晶質即非晶。 <電氣特性結果> 對於所得之元件,使用KEYSIGHT TECHNOLOGIES公司製造之B1505(HVSMU(High-voltage Source Measure Unit,高電壓源測量單元)、HCSMU(Heavy-current Source Measure Unit,強電流源測量單元)、MFCMU(Multi-frequency Capacitance Measure Unit,多頻電容測量單元)、MPSMU(Medium-power Source Measure Unit,中等功率源測量單元)搭載)、偏壓T(N1272A)、電路切換機(N1258A)、及Cascade公司製造之高電壓探針儀EPS 150 TESLA,對電壓(V)-電流特性(J)及電壓(V)-容量(C)特性進行測定。又,對以下之各項目進行評價。將結果示於表2-1。 但是,於測定時上述各SMU或CMU配置於肖特基電極側,且施加偏壓。歐姆電極側為施加0 V之狀態。 (1)載子濃度之測定 使用上述裝置及上述之CV測定取得載子濃度。製作於縱軸取A2 /C2 ,於橫軸取施加電壓V之曲線圖,利用以0 V~2 V之間為起點且直線之斜率與-2/(εr ε0 Ndepl )成正比這一情況,設為載子濃度n=Ndepl 而求出半導體層之載子濃度。載子濃度如表2-1所示般為1.0×1014 cm-3 。又,可根據CV測定之行為確認半導體為n型。 再者,於CV測定時使用下述B1505之CMU單元,藉由偏壓T將電壓重疊而實施測定。測定頻率使用1 kHz,AC振幅設為0.03 V。 可確認本半導體元件滿足下述式(I)。再者,根據上述內容,介電常數由InGaZnO之相對介電常數16算出,Ve 設為0.1 V,L設為200 nm,從而確定了大小關係。 [數14](2)特性溫度之測定 按照前文所述之方法求出特性溫度。利用上述裝置之HCSMU,以向元件施加正向偏壓之方式(HCSMU施加正電壓)施加至0 V~3 V。於縱軸取LogJ-LogV之差量值(LogJ1 -LogJ2 )/(LogV1 -LogV2 )即J-V特性之『冪』,且於橫軸取V。於此,J意指電流密度(A/cm2 ),為測定電流值(A)除以上述電極之有效面積所得之值。J1 、J2 、V1 、V2 為測定點1、2之電流密度及施加電壓值。於2 V~3 V之範圍內平均之『冪』為2.5,本區間之『冪』之最大最小值相對於平均值為±0.5,故視作本半導體層可作為於傳導度下端具有帶尾能階之半導體而適用於前文所述之式(5)。根據前文所述之式(5),『冪』2.5等於I+1,I=Tc/T,測定時之實際溫度為300 K,故求出特性溫度為450 K。 (3)耐壓之確定 如前文所述,耐壓可藉由測定崩潰電壓(V),並除以L之長度而求出。於本肖特基能障二極體之情形時,在掃引逆向電壓之情形時,將達到1×10-3 A之電流值之最初之電壓值定義為崩潰電壓。使用HVSMU,向逆向施加電壓時,由於-62 V下電流值為1×10-3 A,故將崩潰電壓定義為-62 V。單位L之耐壓為除以200 nm所得之絕對值即3.1 MV/cm。 (4)正向導通電阻Ron@2 V之確定 如前文所述,利用上述裝置之HCSMU,以向元件施加正向偏壓之方式(HCSMU施加正電壓)施加至0 V~2 V。測定施加2 V時之電流密度J2V ,定義為正向導通電阻Ron@2 V=2[V]/J2 V [A/cm2 ]進行計算。 (5)漏電流值@-5 V之確定 使用HVSMU,求出向逆向施加-5 V之電壓時之電流密度。由於為   -5.0×10-8 A/cm2 ,故取絕對值,確定漏電流值@-5 V為5.0×10-8 A/cm2 。 實施例2~5、9、18~19 除如表2-1,2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-1,2-2。又,該等實施例之半導體元件滿足式(I)。 實施例6 除如表2-1所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-1。又,該實施例之半導體元件滿足式(I)。 於該實施例中,將實施例1之歐姆電極自Mo變更為Ti。 評價L時,可確認藉由Ti電極之奪氧,包含InGaZnO之TEM像對比度短於200 nm,且半導體層之厚度為180 nm。 實施例7 除如表2-1所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-1。又,該實施例之半導體元件滿足式(I)。 於實施例中,在製作肖特基電極時之濺鍍Pd時,未以Ar及O2 混合氣體進行濺鍍,70 nm自始至終僅使用Ar成膜。 其結果,於InGaZnO/PdO界面上自InGaZnO側向Pd,XPS之Pd光譜中之來自氧之峰值伴隨著InGaZnO所包含之氧濃度平緩地減少,無法斷定Pd中含有氧。又,藉由EDX像觀察到Pd之區域中,明確地不存在可看見TEM像之對比度之區域。由此,判斷肖特基電極為70 nm左右之包含Pd之層。如表2-1所示般記為Pd。 實施例8 將電阻率0.001 Ω·cm之n型Si基板(直徑4英吋,厚度250 μm)安裝於濺鍍裝置(CANON ANELVA製造:E-200S),成膜以下之積層電極作為歐姆電極層。但是對於基板反面,為了消除測定時與探針儀之接觸電阻,而進行Ti100 nm/Au50 nm處理。首先,於DC50 W、Ar環境下成膜15 nm之Ti,其次,於DC50 W、Ar環境下成膜50 nm之Ni,最後,作為肖特基電極,於DC50 W、Ar環境下成膜20 nm之Mo。 繼而,將該基板與半導體用區域遮罩一起放置於濺鍍裝置(ULVAC製造:CS-200),成膜200 nm之InGaZnO(1:1:1)作為耐壓層(半導體層)。成膜條件設為:DC300 W、Ar與H2 O之混合氣體環境(H2 O濃度:1體積%)。濺鍍靶-基板間距離(TS間隔)設為80 mm。取出該基板,使用電氣爐於空氣中300℃之條件下退火1小時。再次將該基板與電極用區域遮罩(孔直徑50 μm)一起放置於濺鍍裝置之後,將Pd靶置於氬氣與氧氣之混合氣體中成膜50 nm之PdO而作為肖特基電極(直徑50 μm)。之後,使用相同遮罩成膜100 μm之Pd電極。成膜條件均設為DC100 W、Ar環境。作為最終處理,實施200℃1小時之大氣下熟化處理。 再者,元件構成成為具有如下特徵之構成,即,如圖2所示般,於半導體層下部具有歐姆電極,自肖特基電極之外周部向歐姆電極面劃垂線時,歐姆電極面處於上述垂線之內側。 對於所獲得之半導體元件,與實施例1同樣地進行評價。將結果揭示於表2-1。又,該實施例之半導體元件滿足式(I)。 實施例10 除如表2-1所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-1。又,該實施例之半導體元件滿足式(I)。 於該實施例中,將半導體層成膜後之退火溫度上升至500℃,結果發現剖面TEM測定時之繞射像發生變化。繞射光點較寬但存在,光點位置相對於複數點之測定部位發生變化。由此判斷本半導體膜為多晶。又,觀察到伴隨著結晶化,半導體層之厚度亦變化為190 nm。 實施例11 除如表2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-2。又,該實施例之半導體元件滿足式(I)。 於該實施例中,肖特基電極使用Ru。形成Si/Ti/Ru/RuO/InGaZnO/Mo之構成。RuO藉由利用Ar與氧氣之混合氣體所進行之濺鍍而形成。 實施例12 除如表2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-2。又,該實施例之半導體元件滿足式(I)。 於該實施例中,肖特基電極使用Ni。形成Si/Ti/Ni/NiO/InGaZnO/Mo之構成。NiO藉由利用Ar與氧氣之混合氣體所進行之濺鍍而形成。 實施例13 除如表2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-2。又,該實施例之半導體元件滿足式(I)。 於該實施例中,使用InSnZnO(1:1:1)靶對半導體層進行濺鍍。 實施例14 除如表2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-2。又,該實施例之半導體元件滿足式(I)。 使用Ga2 O3 靶對半導體層進行濺鍍。由於為絕緣性之濺鍍靶,故變為DC300 W而使用RF(Radio Freqency,射頻)300 W之成膜條件。 實施例15 除如表2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-2。又,該實施例之半導體元件滿足式(I)。 於該實施例中,將半導體層成膜時之環境設為Ar100體積%,將半導體退火之溫度設為帶域中150℃。使用Ga2 O3 靶對半導體層進行濺鍍。由於為絕緣性之濺鍍靶,故變為DC300 W而使用RF300 W之成膜條件。 實施例16 除如表2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-2。又,該實施例之半導體元件滿足式(I)。 於該實施例中,使用InAlO(93:7)靶對半導體層進行濺鍍。發現所得之剖面TEM測定時之繞射像發生變化。繞射光點較寬但存在,且光點位置相對於複數點之測定部位發生變化。但,即便於膜厚方向取得繞射像,亦未觀察到光點位置之變化。由此判斷本半導體膜為多晶(柱狀)。 實施例17 除表2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-2。又,該實施例之半導體元件滿足式(I)。 於該實施例中,使用InGaO(1:1)靶對半導體層進行濺鍍。又,為獲得結晶性,將退火溫度高溫化至600℃。伴隨此,與實施例8同樣地設為如圖2所示般使PdO肖特基電極位於半導體層上部之構成。其目的在於,藉由高溫將PdO還原成Pd,以抑制肖特基阻隔性降低。 發現所得之剖面TEM測定時之繞射像發生變化。繞射光點較寬但存在,且光點位置相對於複數點之測定部位發生變化。但,即便於膜厚方向取得繞射像,亦未觀察到光點位置之變化。由此判斷本半導體膜為多晶(柱狀)。 實施例20 除如表2-2所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表2-2。 於該實施例中,設為具有如下特徵之構成,即,如圖3所示般,於半導體層上部具有肖特基電極,自肖特基電極之外周部向歐姆電極面劃垂線時,歐姆電極面處於上述垂線之外側。 雖然滿足式(I),但與實施例8相比觀察到耐壓之降低及漏電流之上升。 [表2-1] [表2-2] 比較例1 除如表3所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於3。 於該實施例中,將InGaZnO之成膜時之環境設為Ar100體積%。又,未實施半導體成膜後之退火。其結果,載子濃度成為式(I)之範圍以外。又,耐壓亦成為0.1 MV/cm,而成為難以適應功率用途之特性。漏電流於施加-5 V時高於測定裝置之依從性電流值100 mA。而無法進行測定。由此,於表3中記為>1.0×10-3 A。 比較例2 除如表3所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表3。 於該實施例中,省略Pd/PdO層之成膜,肖特基電極成為Ti。結果,雖然觀察到整流特性,但載子濃度成為式(I)之範圍以外。又,漏電流較高,耐壓亦達到0.3 MV/cm,而成為難以適應功率用途之特性。 比較例3 除如表3所示般變更成膜條件以外,與實施例1同樣地製造半導體元件並進行評價。將結果揭示於表3。 於該實施例中,使用In2 O3 靶對半導體層進行濺鍍。發現所得之剖面TEM測定時之繞射像發生變化。繞射光點較寬但存在,且光點位置相對於複數點之測定部位發生變化。但,即便於膜厚方向取得繞射像,亦未觀察到光點位置之變化。由此判斷本半導體膜為多晶(柱狀)。 關於電氣特性,載子濃度較高,所製作之肖特基二極體未獲得整流比,無法以CV測定進行載子濃度測定。又,由於正向之『冪』亦於2~3 V範圍內持續維持2以下之值,故判斷式(5)之關係性不成立,視作無法評價特性溫度。觀察到耐壓之降低及漏電流之上升。 [表3] [產業上之可利用性] 本發明之半導體元件可使用於肖特基能障二極體及接面電晶體。進而,該等可使用於電子電路,利用於各種電氣機器。 於上述中詳細說明了若干本發明之實施形態及/或實施例,業者在不實質性地脫離本發明之新穎之教導及效果的情況下,可容易地對該等作為示例之實施形態及/或實施例施加多種變更。因此,該等多種變更包含於本發明之範圍。 將成為本案之巴黎優先權之基礎之日本申請案說明書之內容全部引用於此。The semiconductor device of the present invention has a pair of ohmic electrodes and a Schottky electrode, and a semiconductor layer that is in contact with the ohmic electrode and the Schottky electrode, and satisfies the following formula (I). [Number 3](where n is the carrier concentration of the above semiconductor layer (cm-3 ), ε is the dielectric constant (F/cm) of the above semiconductor layer, Ve Is the forward effective voltage (V) between the ohmic electrode and the Schottky electrode, and q is the basic charge (1.602×10)-19 C), L is the distance (cm) between the ohmic electrode and the Schottky electrode. The lower limit of n may be 0, but preferably 1 × 1010 the above. More preferably, it satisfies the following formula (I-1), and further preferably satisfies the following formula (I-2). [Number 4][Number 5]In the above formula, the carrier concentration is measured by CV (capacitance-voltage) and is calculated using the following formula (refer to APPLIED PHYSICS LETTERS, 101, 113505 (2012)). [Number 6]A: area of the portion where the Schottky electrode and the ohmic electrode are repeated (cm2 C: The measured capacitance value (F) εs : Relative dielectric constant (-) ε0 : dielectric constant of vacuum (8.854×10)-14 F/cm) NDepl : carrier concentration (cm-3 ) VBi : Built-in voltage (V) k: Boltzmann constant (8.617×10)-5 eV/K) T: sample temperature (K) during measurement q: basic charge (1.602×10)-19 C) V: The applied voltage (V) L can be obtained by the method disclosed in the examples. Ve As described below, it can be 0.1 V. Regarding the dielectric constant ε, as long as the composition and the crystal system of the semiconductor type are determined, the relative dielectric constant of the literature value can be used to determine the product of the relative dielectric constant and the dielectric constant of the vacuum. Further, when the number of reports in the literature is small or the difference is large depending on the report case, actual measurement can also be performed. When the actual measurement is performed, the capacitance value of the film thickness (L) of three or more points can be measured by the film thickness dependence measured by CV, and if C/A is plotted on the vertical axis, When 1/L is plotted on the horizontal axis, the slope becomes the dielectric constant ε. In order to make the semiconductor element satisfy the formula (I), the carrier concentration in the semiconductor layer is lowered. Specifically, the dopant concentration in the semiconductor is lowered. For example, in the case of a semiconductor in which a hydrogen atom or an oxygen defect in a semiconductor functions as a dopant as in an oxide semiconductor, a film having few defects and a high film density is effective for reducing the carrier concentration. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a schematic cross-sectional view showing a semiconductor device according to an embodiment of the present invention. The semiconductor element 1 (vertical) sequentially has a Schottky electrode 10, a semiconductor layer 30, and an ohmic electrode 20. Further, a conductive substrate 40 is provided on the side opposite to the side of the semiconductor layer 30 of the Schottky electrode 10. Fig. 2 is a schematic cross-sectional view showing a semiconductor device according to another embodiment of the present invention. The semiconductor element 2 (vertical) sequentially has a Schottky electrode 10, a semiconductor layer 30, and an ohmic electrode 20. Further, the conductive substrate 40 is provided on the side opposite to the side of the semiconductor layer 30 of the ohmic electrode 20. Further, the ohmic electrode 20 has an insulating layer 50 on both sides thereof, and the ohmic electrode 20 is formed in one layer with the insulating layers 50 on both sides. The semiconductor element 3 of FIG. 3 differs from the element 2 of FIG. 2 only in the case where the width of the ohmic electrode 20 is wide. Fig. 4 is a schematic perspective view showing a semiconductor element as another embodiment of the present invention. The semiconductor element 4 (horizontal type) is disposed on the first surface of the first and second surfaces facing the semiconductor layer 30, and the Schottky electrode 10 is disposed at a distance from the ohmic electrode 20. Further, an insulating substrate 60 is provided on the second surface of the semiconductor layer 30. In the semiconductor device of the present invention satisfying the above formula (I), the initial carrier concentration of the semiconductor layer is small, and the exogenous carrier functions as a main factor of conduction. The well density of the semiconductor layer is small and does not hinder the conduction of the exogenous carrier. Further, in Patent Document 1, there is a relationship of the following formula, and there is a problem in the controllability of the carrier concentration based on the previous carrier concentration design guide of the unipolar power device. [Number 7](where n, ε, Ve , q and L are the same as in the formula (I). The semiconductor device of the present invention has a small reverse leakage current and a low forward conduction resistance, and can extract a large current. Moreover, even if an inexpensive germanium substrate or a metal substrate is used as the conductive substrate, good rectifying characteristics are exhibited. Further, even when the oxide semiconductor layer is formed into a film having excellent productivity such as sputtering, it exhibits good rectifying characteristics. The semiconductor device of the present invention is particularly excellent for use in a vertical Schottky barrier diode. <Regarding Formula (I)> Generally, in the insulator in which no carrier is present, the following formula (1) holds. JIns =(9/8)με(V2 /L3 ) (1) JIns : Current density (A/cm2 ) μ: mobility (cm2 /V·s) ε: dielectric constant of the substance (F/cm) V: applied voltage (V) L: thickness (cm) of the region through which the current flows. On the other hand, regarding the conductor in which the carrier is present, the following formula (2) holds. JOhm =qnμ(V/L) (2) JOhm : Current density (A/cm2 q: basic charge (1.602 × 10-19 C) n: carrier concentration (cm-3 ) μ: mobility (cm2 /V·s) V: Applied voltage (V) L: Thickness (cm) of the region through which the current flows. Yu JIns =JOhm Under the condition, the following formula (3) holds. [Number 8](In the formula, n, ε, V, q, and L are the same as in the formulas (1) and (2). Therefore, when the following formula (4) is established, it means J.Ins >JOhm The role of insulating conduction is greater. That is, it means that the exogenous carrier functions as a main factor of conduction. [Number 9](where n, ε, V, q, and L are the same as in equations (1) and (2)) for Schottky barrier diodes and junction field effect transistors (JFETs) that exhibit rectification characteristics in a single pole. There is a drift region in the metal oxide film semiconductor field effect transistor (MOSFET). Generally, in the drift region, the relationship of the above formula (2) holds. In this case, the applied voltage V means the voltage applied to the drift layer. In the above formula (I), V will bee Defined as the forward effective voltage, but it refers to the voltage, that is, the built-in voltage V for canceling the band bending is removed with respect to the applied voltage V in consideration of the actual device configuration.Bi The effective voltage to the drift layer after the action. In Schottky barrier diodes, junction field effect transistors (JFETs), metal oxide semiconductor field effect transistors (MOSFETs), etc., there are a pair of ohmic electrodes and Schottky between the semiconductor layer devices. In the electrode, as long as the above formula (I) is established, the exogenous carrier functions as a main factor of electrical conduction. Dielectric constant ε-based semiconductor relative permittivity εr Dielectric constant ε with vacuum0 (8.854×10-14 The product of (8.854E-14) [F/cm]). εr The parameters are different depending on the material, but are preferably from 3 to 20, more preferably from 5 to 16, more preferably from 9 to 13. If the relative dielectric constant is too low, there is a small amount of injection of the exogenous carrier, and a high current cannot be obtained. If the relative dielectric constant is too large, there is an increase in parasitic capacitance or a hysteresis in current characteristics. About the forward effective voltage Ve If the actual forward characteristics are used, the applied voltage to the unipolar device is usually about 0.5 V to 1.5 V, and the built-in voltage V isBi Usually 0.7 to 1.3 V, you can put Ve It is considered to be around 0.1 V. The value of the basic charge is 1.602×10-19 C /, so if εr Assuming 10, in view of formula (I), the upper limit of the carrier concentration n is determined by the interval L between one of the semiconductor layers and the ohmic electrode and the Schottky electrode, as shown in Table 1. [Table 1] L is preferably 10 nm < L < 100000 nm, more preferably 20 nm < L < 10000 nm, further preferably 30 nm < L < 1000 nm, and most preferably 50 nm < L < 300 nm. When the inter-electrode spacing L is too short, there is a problem in terms of withstand voltage. If L is too large, the current value is lowered or the thickness of the semiconductor layer in the vertical element is increased to cause time consuming film formation. L and n preferably satisfy the relationship represented by the following formula (Ia), more preferably satisfy the relationship represented by the following formula (Ib), and further preferably satisfy the relationship represented by the following formula (Ic); Preferably, the relationship shown by the following formula (Id) is satisfied. [Number 10](where n, ε, Ve , q and L are the same as in the formula (I). When n is too low, the trap existing in the inside of the semiconductor layer has an effect, and the effect of the diffusion current is large, and the current characteristics are deteriorated. On the other hand, if n becomes εV of the formula (I)e /qL2 As described above, the effect of the drift current is increased, and it is difficult to produce the effect of the present invention as it is close to the previous operational characteristics. <Withstand Voltage of Semiconductor Element> The semiconductor element of the present invention has a pair of ohmic electrodes and a Schottky electrode between the semiconductor layers. Compared with the previous power devices, the withstand voltage V is low due to the designed carrier concentration.BD Design relative to VBD ~Ec L/2 becomes VBD ~Ec L, it is expected to compare with the same L and increase the withstand voltage by about 2 times. Here, Ec For maximum insulation damage to the electric field, L is the length between the electrodes. Moreover, in the prior power device, since the initial carrier concentration is high, the leakage current when the reverse bias is applied is large, and when the peripheral portion (side surface) of the Schottky electrode is perpendicular to the ohmic electrode surface, It is difficult to obtain a component structure in which the ohmic electrode is covered in a plane perpendicular to the Schottky surface. In the present invention, the initial carrier concentration in the semiconductor layer is low, and when the forward voltage is applied, the external carrier is implanted only in the ohmic electrode surface when the peripheral portion of the Schottky electrode is perpendicular to the ohmic electrode surface. It is included in the range from the vertical line of the Schottky surface. On the other hand, when a reverse bias is applied, carriers are not present throughout the entire semiconductor layer, so the influence of leakage current due to rewinding is small. Fig. 5 is a view for explaining an electrode surface of the semiconductor element of Fig. 2. In FIG. 5, the outer peripheral portion of the Schottky electrode is indicated by the symbol 12, and the ohmic electrode surface is indicated by the numeral 22. A perpendicular line drawn from the outer peripheral portion 12 of the Schottky electrode to the ohmic electrode surface 22 is indicated by the symbol A. In a vertical power device, generally, the lower portion of the semiconductor layer is an ohmic electrode, but when the ohmic electrode is inside the vertical line drawn from the Schottky electrode, the Schottky electrode can be easily used for the lower portion of the semiconductor layer. Further, it is known that an electric field absorbing structure such as a guard ring is used in a normal power device to reduce the reverse leakage current. With such a configuration, the electric field mitigation structure which is a process defect can be omitted or reduced. In a power device in which the externally-induced carrier becomes the dominant unipolar, the withstand voltage becomes V as described above.BD ~Ec L, so according to the length between the electrodes L and the withstand voltage VBD The measurement result can easily determine the dielectric breakdown electric field. Here, the withstand voltage of the unit L corresponds to the dielectric breakdown electric field. If the withstand voltage per unit film thickness is high, L can be reduced when designing the same withstand voltage element, so that the injection of the externally-induced carrier is increased, and the element having lower resistance can be provided. The withstand voltage of the unit L is preferably 0.5 MV/cm or more, more preferably 0.8 MV/cm or more, still more preferably 1.0 MV/cm or more, and particularly preferably 3.0 MV/cm or more. The withstand voltage of the unit L can be obtained by measuring the breakdown voltage (V) and dividing by the length of L. For example, in the case of a Schottky barrier diode, it will have reached 1×10 when sweeping the reverse voltage.-3 The initial voltage value of the current value of A is defined as the breakdown voltage. Further, the withstand voltage of the unit L can be adjusted according to the material selection of the semiconductor layer. In the present invention, when the material of the semiconductor layer is a band gap of 1 eV or more and contains an amorphous or polycrystalline semiconductor layer, it can be 0.5 MV/cm or more. When it is a material having a band gap of 2 eV or more, it is 1.0 MV/cm or more, and when it is a band gap of 2 eV or more and contains an amorphous or polycrystalline semiconductor layer, it can reach 3.0 MV/cm or more. <Characteristic Temperature> The characteristic temperature is a parameter indicating the characteristics of the tail energy level at the lower end of the conduction band specific to amorphous or polycrystalline crystals, and is a semiconductor having a tail-level energy-dependent carrier at the lower end of the conduction band. The characteristics of the following formula (5). [Number 11]J: current density (A/cm2 u: mobility (cm2 /V·s) Nc : Effective state density of semiconductors (cm-3 ) Nt : the tail energy density of the lower end of the conduction band (cm-3 ε: dielectric constant of material (F/cm) V: applied voltage (V) L: thickness of region through which current flows (cm) e: basic charge (1.602×10)-19 C) I: Tc/T Tc: characteristic temperature (K) T: actual temperature (K) The characteristic temperature Tc is a parameter of Tc>T, which has a large number of energy at the end of the tail, which prevents the injection of the externality by the trap. When the carrier is transmitted, it becomes a larger value. When the current-voltage measurement is performed, it can be seen from the equation (5) that the slope of the curve of Log(J)-Log(V) is I+1. Therefore, I is obtained from the slope, and Tc is calculated. However, the case where the value of Tc is fixed with respect to a continuous range of application voltage becomes an indicator that the semiconductor layer has a tail energy level. It is preferably Tc < 1500 K, more preferably Tc < 900 K, and further preferably Tc < 600 K. If the value of Tc is large, there is an increase in the number of carriers due to the trapping of the tail energy level, and the device characteristics are high resistance. The characteristic temperature can be determined from the slope of the curve of Log(J)-Log(V) by performing current-voltage measurement. The characteristic temperature can be lowered by increasing the short-range order of the atomic structure in amorphous or polycrystalline semiconductors. For example, in the case of an amorphous metal oxide semiconductor, a film having a low density tends to have a short distance order and a characteristic temperature tends to be high. It has been confirmed that in the amorphous metal oxide semiconductor formed by sputtering, the density is related to the film formation conditions. The closer the target-substrate distance is, the lower the sputtering pressure is, the higher the substrate temperature at the time of film formation or the higher the annealing temperature after film formation, or the higher the applied voltage applied to the target at the time of sputtering film formation, the easier it is to form. High density film. Further, when sputtering is performed, 0.1 to 10% by volume of H is added.2 Or H2 As a sputtering gas, O is easy to obtain a film of high density. When the amorphous or polycrystalline semiconductor layer contains a metal oxide semiconductor of one or more elements selected from the group consisting of In, Zn, Ga, and Sn, the s-track having a high target property can be utilized, so that it is less susceptible to the disorder of the periodic potential. Influence, the characteristic temperature tends to be low. <Lamination of Drift Layer (Limited to Vertical Element)> The following semiconductor element (vertical) can be obtained, that is, having a carrier concentration of the following formula (6)L Lower semiconductor layer (L1 , L2 ,...Ln )(nL And Ln Indicates the carrier concentration and film thickness of the layer with the lower concentration of the carrier at the nth when the Schottky electrode is counted toward the ohmic electrode) and the carrier concentration nh Higher semiconductor layer (d1 , d2 ,...dN-1 )(nh And dn The structure in which the carrier concentration and the film thickness of the layer having the higher carrier concentration of the nth carrier are repeated on the drift layer when the Schottky electrode is counted toward the ohmic electrode is shown. [Number 12](in the formula, nL The carrier concentration of the layer at the lower concentration of the nth carrier when the Schottky electrode is counted toward the ohmic electrode, and ε represents the dielectric constant of the semiconductor layer having the lower carrier concentration of the nth, Ve Indicates the effective voltage of the semiconductor layer applied to the nth carrier with a lower concentration (can be set to Ve =0.1 V), q represents the basic charge, Ln The film thickness of the semiconductor layer having a lower carrier concentration of the nth layer is expected to be higher than the drift of the single layer by the lamination, and the resistance value can be expected to be reduced. In this case, Ln Preferably 10 nm < Ln <1000 nm, more preferably 20 nm<Ln <300 nm, and more preferably 30 nm<Ln <200 nm, especially 30 nm<Ln <100 nm. If Ln If it is too short, the difference will become larger if Ln If it is too long, the resistance value will become higher. Again, dn Preferably 3 nm<dn <30 nm, more preferably 5 nm<dn <10 nm. If dn If it is too long, the depletion layer does not spread to the entire region from the Schottky electrode to the ohmic electrode when a reverse bias is applied, which causes a problem in terms of withstand voltage. If dn Too short, there is no play as Ln With Ln + 1 The function of the spacer layer does not function as a laminate structure. nh It is preferably the following formula (6-a), more preferably the following formula (6-b), and still more preferably the following formula (6-c). [Number 13](wherein ε represents the dielectric constant of the semiconductor layer having a higher concentration of the nth carrier, Ve Indicates the effective voltage of the semiconductor layer applied to the nth carrier with a higher concentration (can be set to Ve =0.1V), q represents the basic charge, dn The film thickness of the semiconductor layer indicating the higher concentration of the carrier of the nth number)h If it is too large, the semiconductor layer having a high carrier concentration suppresses the extension of the depletion layer when the reverse bias is applied, and it is difficult to maintain the withstand voltage. If nh If it is too small, it is necessary to inject an exogenous carrier into the layer with a higher concentration of the carrier during the forward application. As a result, a plurality of semiconductor layers having a lower concentration of the carrier operate as a layer having a lower carrier concentration and the resistance value. Increased. Preferably, the layer with the Schottky electrode is a layer having a lower carrier concentration. <Series connection of semiconductor elements> In the voltage withstand design of the conventional unipolar power device, when the voltage with a rated withstand voltage is applied, the electric field strength of the semiconductor interface on the Schottky metal side reaches the vicinity of the dielectric breakdown electric field, making it difficult to carry out the semiconductor element. Link. For example, in the case of a Schottky barrier diode, it is difficult to obtain a withstand voltage of 600 V or more even if a plurality of components having a 600 V withstand voltage are connected in series. In the semiconductor device (power device) in which the initial carrier concentration of the present invention is low and the external injection carrier is used, in the case of a plurality of series connection, the breakdown voltage is multiplied by the rated withstand voltage corresponding to the number of the connected ones. And increase. Therefore, it is possible to easily provide the required pressure-resistant component. <Composition Layer of Semiconductor Element> (1) Semiconductor Layer The semiconductor layer is not particularly limited, and preferably contains polycrystalline or amorphous. Further, it is preferable to contain a metal oxide semiconductor, and more preferably a metal oxide semiconductor containing an element selected from one or more selected from the group consisting of In, Zn, Ga, Sn, and Al. When it is amorphous, the large-area uniformity is excellent, and the impact ionization at the time of applying a reverse bias is lowered and the withstand voltage is improved. If it is polycrystalline, it has a large area uniformity and a good conduction property. When a semiconductor layer is produced from a metal oxide semiconductor, a film formation method excellent in a large area using a sintered sputtering target can be employed. By using a metal oxide semiconductor containing an element selected from one or more of In, Zn, Ga, Sn, and Al in a semiconductor layer, the conduction characteristics of the s orbit of the metal element can be utilized, so that even if it is amorphous or The crystal also forms a semiconductor layer having overlapping tracks and excellent conduction characteristics. The metal oxide semiconductor may contain one or more metal oxides. Examples of the metal oxide include oxides of In, Sn, Ge, Ti, Zn, Y, Sm, Ce, Nd, Ga, and Al. It is preferable to contain one or more elements selected from the group consisting of In, Zn, Ga, and Sn. The metal of the metal oxide semiconductor may substantially contain one or more selected from the group consisting of In, Sn, Ge, Ti, Zn, Y, Sm, Ce, Nd, Ga, and Al. Further, the metal may be, for example, 95 atom% or more, 98 atom% or more, or 99 atom% or more, and may be one or more selected from the group consisting of In, Sn, Ge, Ti, Zn, Y, Sm, Ce, Nd, Ga, or Al. . The metal oxide constituting the metal oxide semiconductor preferably has an atomic ratio satisfying the following formulas (A) to (C). In the case of such a composition, it is possible to set a high withstand voltage and a low on-resistance. 0≦x/(x+y+z)≦0.8 (A) 0≦y/(x+y+z)≦0.8 (B) 0≦z/(x+y+z)≦1.0 (C) (where x represents a selected from In, Sn, Ge, and The number of atoms of one or more elements in Ti, y represents the number of atoms of one or more elements selected from the group consisting of Zn, Y, Sm, Ce, and Nd, and z represents the number of atoms selected from one or more of Ga and Al) When x is more than 0.8, when x is In or Sn, the insulation of the metal oxide becomes low, the Schottky junction is not easily obtained, and when x is Ge or Ti, there is a metal oxide. The insulation becomes high and becomes a cause of heat generation due to ohmic loss. More preferably, the above compositions (A) to (C) are the following formulas (A-1) to (C-1), respectively. 0≦x/(x+y+z)≦0.7 (A-1) 0≦y/(x+y+z)≦0.8 (B-1) When z is Ga: 0.02≦z/(x+y+z)≦1.0 z is Al: 0.005≦z /(x+y+z)≦0.5 (C-1) (wherein x, y and z are the same as the above formulae (A) to (C)) When z is Ga, if it is less than 0.02, there is oxygen in the metal oxide Easy to get rid of, uneven electrical characteristics. Further, it is preferred that the above components (A) to (C) are the following formulas (A-2) to (C-2), respectively. 0.1≦x/(x+y+z)≦0.5 (A-2) 0.1≦y/(x+y+z)≦0.5 (B-2) 0.03≦z/(x+y+z)≦0.5 (C-2) (where x and y are The above formulae (A) to (C) are the same, and z is Ga). The above compositions (A) and (C) are preferably the following formulas (A-3) and (C-3), respectively. 0≦x/(x+y+z)≦0.25 (A-3) 0.3≦z/(x+y+z)≦1.0 (C-3) (wherein x, y, and z are the same as the above formulas (A) and (C)) The metal oxide of the metal oxide semiconductor layer may be amorphous or crystalline, and the crystal may be microcrystalline or single crystal. Preferably, the metal oxide is amorphous or microcrystalline. When the metal oxide is used as a single crystal, a method in which crystal growth is started from a seed crystal, or MBE (molecular beam epitaxy) or PLD (pulse laser deposition) is used. If SiO2 Crystal growth on a surface or a metal surface is liable to cause crystal defects, and when used as a device for energization in the longitudinal direction, there is a problem that the crystal defect causes a defect. In SiO2 In the case of crystal growth on the surface or the metal surface, the heating temperature, time, and the like are appropriately adjusted so that the particle diameter does not become excessive. On the other hand, in the case of amorphous, even if a dangling bond is present, since it does not exist as a crystal defect, it is possible to alleviate the unevenness of electrical characteristics or the characteristic deterioration of a large amount. Further, since the metal oxide and the Si semiconductor have different covalent bonds and have high ionic bonding properties, the energy level by the dangling bonds approaches the conductive tape or the full body. Therefore, the metal oxide has a smaller difference in electrical characteristics such as mobility due to structure than Si or SiC. When such a property of the metal oxide is actively utilized, a large current diode or a switching element having high withstand voltage and high reliability can be provided at a high yield even in the case of a single crystal. Here, "amorphous" means that a cross section of the metal oxide layer in the film thickness direction is obtained, and when it is evaluated by an electron beam diffraction method such as a transmission electron microscope, it is impossible to obtain a distinct diffracted light. Pointer. It is preferable to obtain a diffraction image from a wide area of about 10 nm from the irradiation region of the electron beam. The so-called obvious light spot refers to a diffraction point with symmetry observed from the diffraction image. Further, "amorphous" also includes a portion having partial crystallization or microcrystallization. When the electron beam is irradiated to the partially crystallized portion, the diffraction image can be confirmed. The term "microcrystalline structure" means that the size of the crystal grain size is submicron or less, and there is no clear grain boundary. By "polycrystalline" is meant that the size of the crystal grain size exceeds the micron size and there is a clear grain boundary. The carrier concentration of each layer constituting the metal oxide semiconductor layer is usually 1 × 1011 ~1×1018 Cm-3 , for example, 1×1013 ~1×1018 Cm-3 . The carrier concentration can be determined, for example, by CV measurement. The properties required for the diode are high-speed switching, high withstand voltage, and low on-resistance, and these characteristics can be combined as long as a semiconductor element using a metal oxide is used. The reason is that the band gap of the metal oxide is originally wide and is high withstand voltage. Further, since the oxygen defect tends to be n-type and the p-type is not easily formed, this case is also advantageous for high-speed switching. In order to lower the on-resistance, it is only necessary to crystallize it to increase the mobility, but it is preferably limited to the extent that the grain boundary cannot be formed. Porosity is often present in the grain boundaries, and polarization occurs when an electric field is formed, which makes the pressure resistance performance lower. In the case where the reduction in withstand voltage is remarkable, it is preferably used directly in the form of amorphous. When it is used as an amorphous material, it depends on the type of the element forming the metal oxide layer. However, the heat treatment conditions may be set to, for example, 500 ° C or less and within 1 hour. By heating at a low temperature of 500 ° C or lower, a stable amorphous state can be obtained. The film thickness of the semiconductor layer is not limited and is usually from 100 to 8000 nm. (2) The metal of the Schottky electrode constituting the Schottky electrode is not particularly limited, and is preferably selected from the group consisting of Pd, Mo, Pt, Ir, Ru, Ni, W, Cr, Re, Te, Mn, Os, Fe, One or more metals (including an alloy) or an oxide of the metal of Rh and Co are more preferably one or more selected from the group consisting of Pd, Pt, Ir, and Ru (including an alloy) or an oxide of the metal. Further, a metal or metal oxide which is in contact with the Schottky which is excellent in the pressure-resistant layer of the oxide semiconductor layer is preferable. More preferably, in combination with an oxide semiconductor, a higher Schottky barrier Pd oxide, Pt oxide, Ir oxide, and Ru oxide are formed. The oxides usually have a semiconductor or an insulator formed by oxidation, but can maintain a high carrier density metal state by selecting a composition or film formation condition, and are formed by contact with an oxide semiconductor. Good Schottky contact. In order to form a good Schottky electrode for the oxide, it is preferred that the carrier concentration of the Schottky electrode is preferably 1018 Cm-3 the above. If not up to 1018 Cm-3 In the case where the contact with the oxide semiconductor layer is p-n junction, the advantage of the Schottky diode such as high-speed response is impaired. The carrier concentration can be obtained, for example, by Hall measurement or the like. The method for producing the metal oxide layer is not particularly limited, and can be preferably used in a method of performing reactive sputtering of the metal target in an oxygen-containing atmosphere. The thickness of the Schottky electrode is usually from 2 nm to 500 nm, preferably from 5 nm to 200 nm. If it is too thin, there is a possibility that the on-resistance at the time of forward bias is increased by the influence of the metal to be contacted. If it is too thick, the on-resistance at the time of forward bias is increased due to its own resistance, or the flatness of the Schottky interface is deteriorated, and the withstand voltage is lowered. Regarding the Schottky electrode, in order to reduce the contact resistance with the substrate or the current extraction electrode and to improve the adhesion, a layer containing a plurality of metals or metal oxides having different compositions may be laminated on the side opposite to the side in contact with the semiconductor layer. (3) The material of the ohmic electrode ohmic electrode is not particularly limited as long as it can perform good ohmic connection with the semiconductor layer, and is preferably one selected from the group consisting of Ti, Mo, Ag, In, Al, W, Co, and Ni. The above metal (including an alloy) or a compound thereof (oxide or the like) is more preferably a metal (including an alloy) or a compound thereof selected from the group consisting of Mo, Ti, Au, Ag, and Al. Further, the ohmic electrode may be formed by a plurality of layers. For example, a Mo electrode layer is used on the side in contact with the semiconductor layer, and in order to extract a large current and to thickly laminate a metal layer such as Au or Al, the layer can serve as a basis for wire bonding. The thickness of the ohmic electrode is usually 10 nm to 5 μm. (4) Film forming method The film forming method of each layer is not particularly limited, and a method of thermal CVD (chemical vapor deposition) or CAT-CVD (catalytic chemical vapor deposition) can be used. CVD method such as deposition method, photo CVD method, atomization CVD method, MO-CVD (Metal-organic Chemical Vapor Deposition), plasma CVD method, etc.; MBE (Molecular Beam Epitaxy) Atomic-level film formation methods such as epitaxial method and ALD (atomic layer deposition); PVD (Physical Vapor Deposition) such as ion plating, ion beam sputtering, and magnetron sputtering Method; a previously known method of using a ceramic step such as a doctor blade method, an injection method, an extrusion method, a hot press method, a sol-gel method, an aerosol deposition method, etc.; a coating method, a spin coating method, a printing method, a spray method Wet method such as electroplating method, plating method, and micellar electrolysis method. In the case of selecting a metal oxide semiconductor, the film formation method of the semiconductor layer is preferably sputtering. The film forming gas is preferably at least one selected from the group consisting of rare gases, oxygen, hydrogen, and water. The distance between the sputtering target and the substrate (TS interval) is preferably from 10 mm to 200 mm. If the TS interval is too short, there is a possibility that the TS cannot be discharged. When the TS interval is too long, the film quality of the semiconductor becomes sparse, and it may become a film having a large characteristic temperature. (5) Substrate The substrate of the semiconductor element is not particularly limited, and a known one can be used. Examples of the substrate include a conductive substrate, a semiconductor substrate, and an insulating substrate. In the vertical semiconductor element, as shown in FIGS. 1 and 2, a conductive substrate can be used. The conductive substrate can be disposed in contact with the Schottky electrode or the ohmic electrode. As the conductive substrate, a substrate which is excellent in surface smoothness such as a tantalum single crystal substrate, a tantalum polycrystalline substrate, or a tantalum crystal substrate can be used. Further, a semiconductor substrate such as a SiC substrate, a GaN substrate, or a GaAs substrate can be used in addition to the germanium substrate. A metal substrate having excellent conductivity such as an Al substrate, a Cu substrate, or a Ni substrate can be used. In view of mass productivity and cost, it is preferable to use a substrate. The germanium substrate has an n-type, an i-type, and a p-type depending on the presence or absence of doping, and when a current flows in the longitudinal direction, it is preferably an n-type or a p-type having a small electric resistance. As the dopant, previously known B, P, Sb, or the like can be used. Especially in the case of reducing the resistance, As or red phosphorus can also be used as a dopant. In the transverse semiconductor device, as shown in FIG. 4, an insulating substrate can be used. The insulating substrate can be disposed in contact with the semiconductor layer. The insulating substrate is not particularly limited as long as it has insulating properties, and the user can be arbitrarily selected without departing from the effects of the present invention. For example, in addition to quartz glass, bismuth borate glass, aluminoborosilicate glass, aluminosilicate glass, etc., an alkali-free glass substrate or a ceramic substrate produced by a melt method or a floating method, it can be used to be resistant. A plastic substrate or the like which is subjected to heat treatment at a temperature of the production step. Further, a dielectric substrate can also be used as the insulating substrate. Examples of the dielectric substrate include a lithium niobate substrate, a lithium niobate substrate, a zinc oxide substrate, a crystal substrate, and a sapphire substrate. Further, a substrate for an insulating film or a dielectric film can be provided on the surface of a metal substrate such as a stainless steel alloy. Further, an insulating film may be formed on the substrate as a base film. As the base film, a single layer or a laminate such as a ruthenium oxide film, a tantalum nitride film, a hafnium oxynitride film, or a hafnium oxynitride film can be formed by a CVD method or a sputtering method. The material of the semiconductor substrate is not particularly limited as long as the smoothness of the surface is maintained. As the semiconductor substrate, the carrier concentration is adjusted to 1 × 1018 Cm-3 The following Si substrate, GaN substrate, SiC substrate, GaP substrate, GaAs substrate, ZnO substrate, Ga2 O3 A substrate, a GaSb substrate, an InP substrate, an InAs substrate, an InSb substrate, a ZnS substrate, a ZnTe substrate, a diamond substrate, or the like. The semiconductor substrate may be single crystal or polycrystalline. Further, it may be a substrate partially containing an amorphous substrate or an amorphous substrate. It can also be used on a conductor substrate, a semiconductor substrate, or an insulating substrate, and a substrate on which a semiconductor film is formed by a method such as CVD (Chemical Vapor Deposition). The substrate may be used on the conductive substrate, the semiconductor substrate, or the insulating substrate, and may have any structure, layer structure, circuit, wiring, electrode, or the like which is composed of a plurality of materials. Examples of the material of the arbitrary structure include a composite material of various metals or insulators such as a metal or an interlayer insulating film which is formed on a large-scale integrated circuit (LSI). The layer as the layer structure is not particularly limited, and an electrode layer, an insulating layer, a semiconductor layer, a dielectric layer, a protective film layer, a stress buffer layer, a light shielding layer, an electron/hole injection layer, and an electron/hole transport layer can be used. A well-known layer such as a light-emitting layer, an electron/hole blocking layer, a crystal growth layer, an adhesion improving layer, a memory layer liquid crystal layer, a capacitor layer, and an electricity storage layer. Examples of the electrode layer include an Al layer, a Si layer, a Sc layer, a Ti layer, a V layer, a Cr layer, a Ni layer, a Cu layer, a Zn layer, a Ga layer, a Ge layer, a Y layer, a Zr layer, and an Nb layer. Mo, Tc, Ru, Rh, Pd, Ag, Cd, In, Sn, Sb, Te, Hf, Ta, W, Re, Os, Ir And a Pt layer, an Au layer, an alloy layer containing one or more metals of the layers, an oxide electrode layer, and the like. It is also possible to increase the carrier concentration of a semiconductor such as an oxide semiconductor or Si for the electrode layer. The insulating layer is generally selected from the group consisting of Al, Si, Sc, Ti, V, Cr, Ni, Cu, Zn, Ga, Ge, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag. An oxide insulating film, a nitride film, or the like of a metal of one or more of the group consisting of Cd, In, Sn, Sb, Te, Hf, Ta, W, Re, Os, Ir, Pt, and Au. The semiconductor layer is not limited to a single crystal, polycrystal, or amorphous crystal state, and widely includes a Si layer, a GaN layer, a SiC layer, a GaP layer, a GaAs layer, a GaSb layer, an InP layer, an InAs layer, an InSb layer, and a ZnS. Layer, ZnTe layer, diamond layer, Ga2 O3 An oxide semiconductor layer such as ZnO or InGaZnO or an organic semiconductor layer such as fused pentene. Examples of the dielectric layer include a lithium niobate layer, a lithium niobate layer, a zinc oxide layer, a crystal substrate layer, a sapphire layer, and BaTiO.3 Layer, Pb(Zr,Ti)O3 (PZT) layer, (Pb, La) (Zr, Ti) O3 (PLZT) layer, Pb(Zr, Ti, Nb)O3 (PZTN) layer, Pb(Ni, Nb)O3 -PbTiO3 (PNN-PT) layer, Pb(Ni, Nb)O3 -PbZnO3 (PNN-PZ) layer, Pb(Mg, Nb)O3 -PbTiO3 (PMN-PT) layer, SrBi2 Ta2 O9 (SBT) layer, (K, Na) TaO3 Layer, (K, Na) NbO3 Layer, BiFeO3 Layer, Bi(Nd, La)TiOx Layer (x=2.5~3.0), HfSiO(N) layer, HfO2 -Al2 O3 Layer, La2 O3 Layer, La2 O3 -Al2 O3 Layers, etc. As the film of the protective film layer, a film which is excellent in insulating properties and low in permeability of water or the like is exemplified, regardless of the inorganic substance or the organic substance. As the protective film layer, for example, SiO2 Layer, SiNx Layer (x=1.20~1.33), SiON layer, Al2 O3 Layers, etc. Examples of the stress buffer layer include an AlGaN layer and the like. Examples of the light shielding layer include a black matrix layer containing a metal, a metal-organic substance, and a color filter layer. Examples of the electron/hole injection layer include an oxide semiconductor layer, an organic semiconductor layer, and the like. Examples of the electron/hole transport layer include an oxide semiconductor layer, an organic semiconductor layer, and the like. Examples of the light-emitting layer include an inorganic semiconductor layer, an organic semiconductor layer, and the like. Examples of the electron/hole blocking layer include an oxide semiconductor layer and the like. Examples of the substrate include a power generation device, a light-emitting device, a sensor, a power conversion device, an arithmetic device, a protection device, an optoelectronic device, a display, a memory, a semiconductor device having a back-end process, a power storage device, and the like. The layer of the layer structure may be a single layer or a layer of two or more layers. The semiconductor device of the present invention can be used as a power semiconductor element, a (rectifier) diode element, a Schottky barrier diode element, an electrostatic discharge (ESD) protection diode, and a transient voltage protection (TVS) protection diode Body, LED, MOSFET, FET, JFET, MOSFET, Schottky source/drain MOSFET -Oxide-Semiconductor Field Effect Transistor, avalanche multiplying photoelectric conversion element, solid-state imaging element, solar cell element, photo sensor element, display element, resistance change memory, and the like. It is also especially suitable for power applications because it can extract large currents. Electronic circuits using the components can be applied to electrical machines, electronic machines, vehicles, power mechanisms, and the like. [Examples] Example 1 An n-type Si substrate (4 inches in diameter and 250 μm in thickness) having a specific resistance of 0.001 Ω·cm was attached to a sputtering apparatus (manufactured by CANON ANELVA: E-200S) to form a laminated electrode below. However, for the back surface of the substrate, in order to eliminate the contact resistance with the probe device during the measurement, Ti 100 nm/Au 50 nm treatment was performed. First, Ti is formed into a film of 15 nm in DC (Direct Current, DC) at 50 W, Ar, and then Pd is formed into a film of 50 nm in a DC 50 W, Ar environment. Finally, as a Schottky electrode, at DC50 W, Ar. With O2 A 20 nm PdO film was formed in a mixed gas atmosphere. Then, the substrate was placed in a sputtering apparatus (manufactured by ULVAC: CS-200) together with a semiconductor region mask, and an InGaZnO (In:Ga:Zn (atomic ratio)=1:1:1 was formed at 200 nm. In the following, the oxide of the composition is referred to as "InGaZnO (1:1:1)", and the other composite oxides are similarly described as the pressure-resistant layer (semiconductor layer). Film formation conditions are set to: DC300 W, Ar and H2 O mixed gas environment (H2 O concentration: 1% by volume). The sputtering target-substrate distance (TS interval) was set to 80 mm. The substrate was taken out and annealed in an electric furnace at 300 ° C for 1 hour in the air. The substrate and the electrode were again placed in a sputtering apparatus with a region mask (pore diameter: 50 μm), and a 150 nm Mo was formed as an ohmic electrode (diameter: 50 μm). Thereafter, an Al electrode of 2 μm was formed using the same mask. The film formation conditions were all set to DC100 W and Ar environment. As a final treatment, an under-tempering treatment at 200 ° C for 1 hour was carried out. Further, the element configuration has a configuration in which a Schottky electrode is provided on the lower portion of the semiconductor layer as shown in FIG. 1, and an ohmic electrode surface is formed when the peripheral portion of the Schottky electrode is perpendicular to the ohmic electrode surface. Located inside the above vertical line. <Interelectrode Distance L> The interelectrode distance L is obtained by a cross-sectional TEM (transmission electron microscope) image and an EDX (energy dispersive X-ray spectroscopy) image of a cross-sectional TEM. It is assumed that the layer containing InGaZnO is a semiconductor layer, the Schottky electrode is a PdO layer, the ohmic electrode is Mo, and the contrast of the TEM cross-section image is defined by EDX and the portion including InGaZnO is a semiconductor layer. Defined as the distance L between the electrodes. Further, the semiconductor layer was sandwiched by Pd and Mo by EDX, and the distance L between the electrodes was 200 nm. When the semiconductor layer is depleted by reverse bias and is biased as a resistive layer by forward biasing, it is confirmed by CV (capacity-voltage) measurement that the thickness should function as a semiconductor in the above-mentioned L. no problem. The minimum capacity value C when the reverse voltage is appliedMin And the maximum capacity value C when a forward voltage is appliedMax , using C/A=εr ×ε0 /d relational expression CMin Corresponding film thickness dMin And CMax Corresponding film thickness dMax Since the difference converges to L±50% with respect to L, it is verified that the distance L between the electrodes is 200 nm. However, the relative dielectric constant of InGaZnO (1:1:1) in the film formation method was confirmed to be 16 according to the film thickness measurement, so ε was used.r =16. It is generally reported that the relative dielectric constant of InGaZnO is about 10 to 19. C: capacity value (F) A: effective area of the electrode (cm2 d: film thickness (cm) ε acting as a semiconductorr : Relative dielectric constant ε0 : Dielectric constant of vacuum, 8.854E-14 [F/cm] Here, the effective area A of the electrode indicates the area of the ohmic electrode and the Schottky electrode which are separated from each other with respect to the semiconductor layer. Regarding this embodiment, the area of the ohmic electrode having a diameter of 50 μm can be regarded as A. Further, in the CV measurement, the CMU (Capacitance Measure Unit) unit of B1505 described below was used, and the voltage was superposed by the bias voltage T to carry out the measurement. The measurement frequency is 1 kHz and the AC amplitude is set to 0.03 V. <Identification of Electrode Type> The identification of the electrode type was carried out after the identification of the above-mentioned semiconductor layer, and the type of the electrode sandwiching the semiconductor layer material was regarded as an ohmic electrode and a Schottky electrode. From the cross-sectional EDX image, it is presumed that the metal or metal compound containing Mo and Pd is an ohmic electrode or a Schottky electrode. Based on the confirmation of the rectification characteristics, it was judged that the Mo side was an ohm and the Pd side was a Schottky electrode type. Further, by XPS (X-ray photoelectron spectroscopy, X-ray photoelectron spectroscopy), the surface of the element was subjected to Ar sputtering to the depth method, and the XPS spectrum was confirmed. From the Mo side to the Mo/InGaZnO interface, the peak of oxygen from the Mo spectrum of XPS is accompanied by a gradual increase in the oxygen concentration of InGaZnO, and the Mo layer away from InGaZnO is focused on more than 90% of the XPS spectrum of Mo. Attributable to pure Mo, the ohmic electrode is set to Mo. On the other hand, in the state of InGaZnO/PdO from the side of InGaZnO to Pd, the peak of oxygen in the Pd spectrum of XPS is not accompanied by a gradual decrease in the oxygen concentration contained in InGaZnO, and a certain degree of oxygen is contained. In Pd. Moreover, in the region where Pd is observed by the EDX image, the contrast of the TEM image is clearly seen, and in the depth direction XPS between the region of pure Pd and the region of InGaZnO, there is an electron density of less than 20 nm. The area of the Pd of pure Pd. Thus, the Schottky electrode is a layer containing Pd or PdO of about 20 nm. As shown in Table 2-1, it is referred to as Pd(PdO). <Evaluation of Crystallinity> The crystallinity was evaluated by an electron beam diffraction method when observing the cross-sectional TEM of the semiconductor layer. A diffraction image is obtained from an area where the electron beam is irradiated in a region having a diameter of 10 nm or more. In the plurality of dots in the direction parallel to the film thickness direction and the cross section, the spot shape cannot be confirmed in the diffraction image, and therefore the semiconductor layer is determined to be amorphous, that is, amorphous. <Electrical characteristic result> For the obtained component, B1505 (HVSMU (High-voltage Source Measure Unit), HCSMU (Heavy-current Source Measure Unit), which is manufactured by KEYSIGHT TECHNOLOGIES, is used. MFCMU (Multi-frequency Capacitance Measure Unit), MPSMU (Medium-power Source Measure Unit), bias voltage T (N1272A), circuit switching machine (N1258A), and Cascade The company's high-voltage probe instrument, EPS 150 TESLA, measures voltage (V)-current characteristics (J) and voltage (V)-capacity (C) characteristics. In addition, the following items were evaluated. The results are shown in Table 2-1. However, each of the SMUs or CMUs described above is disposed on the Schottky electrode side at the time of measurement, and a bias voltage is applied. The ohmic electrode side is in a state of applying 0 V. (1) Measurement of carrier concentration The carrier concentration was obtained by the above apparatus and the above-described CV measurement. Made on the vertical axis, take A2 /C2 , taking the curve of the applied voltage V on the horizontal axis, using the slope between 0 V and 2 V as the starting point and the slope of the line and -2/(εr ε0 NDepl In proportion to this case, set the carrier concentration n=NDepl The carrier concentration of the semiconductor layer was determined. The carrier concentration is 1.0×10 as shown in Table 2-1.14 Cm-3 . Further, it is confirmed that the semiconductor is n-type based on the behavior of the CV measurement. Further, in the CV measurement, the CMU unit of the following B1505 was used, and the voltage was superposed by the bias voltage T to carry out the measurement. The measurement frequency is 1 kHz and the AC amplitude is set to 0.03 V. It was confirmed that the present semiconductor element satisfies the following formula (I). Furthermore, according to the above, the dielectric constant is calculated from the relative dielectric constant 16 of InGaZnO, Ve Set to 0.1 V and L to 200 nm to determine the size relationship. [Number 14](2) Measurement of characteristic temperature The characteristic temperature was determined by the method described above. The HCSMU using the above device is applied to 0 V to 3 V in a manner of applying a forward bias to the device (a positive voltage is applied to the HCSMU). Take the difference between LogJ-LogV on the vertical axis (LogJ1 -LogJ2 )/(LogV1 -LogV2 ) is the "power" of the J-V characteristic, and takes V on the horizontal axis. Here, J means current density (A/cm)2 ), the value obtained by dividing the current value (A) by the effective area of the above electrode. J1 , J2 V1 V2 To measure the current density of points 1, 2 and the applied voltage value. The average power of the range from 2 V to 3 V is 2.5, and the maximum and minimum of the power of this interval is ±0.5 with respect to the average value. Therefore, the semiconductor layer can be regarded as having a tail at the lower end of the conductivity. The semiconductor of the energy level is applicable to the above formula (5). According to the above formula (5), "power" 2.5 is equal to I+1, I=Tc/T, and the actual temperature at the time of measurement is 300 K, so the characteristic temperature is found to be 450 K. (3) Determination of withstand voltage As described above, the withstand voltage can be obtained by measuring the breakdown voltage (V) and dividing by the length of L. In the case of the Ben Schottky barrier diode, it will reach 1×10 when sweeping the reverse voltage.-3 The initial voltage value of the current value of A is defined as the breakdown voltage. When using HVSMU, when applying voltage to the reverse direction, the current value at -62 V is 1 × 10-3 A, so the breakdown voltage is defined as -62 V. The withstand voltage of unit L is the absolute value obtained by dividing by 200 nm, that is, 3.1 MV/cm. (4) Determination of forward conduction resistance Ron@2 V As described above, the HCSMU using the above device is applied to 0 V to 2 V by applying a forward bias to the element (a positive voltage is applied to the HCSMU). Measuring the current density when applying 2 V2V , defined as positive conduction resistance Ron@2 V=2[V]/J2 V [A/cm2 ]Calculation. (5) Determination of leakage current value @-5 V Using HVSMU, the current density when a voltage of -5 V was applied in the reverse direction was obtained. Since it is -5.0×10-8 A/cm2 Therefore, take the absolute value and determine the leakage current value @-5 V is 5.0×10-8 A/cm2 . (Examples 2 to 5, 9, and 18 to 19) A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Tables 2-1 and 2-2. The results are disclosed in Tables 2-1, 2-2. Further, the semiconductor elements of the embodiments satisfy the formula (I). Example 6 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-1. The results are disclosed in Table 2-1. Further, the semiconductor element of this embodiment satisfies the formula (I). In this embodiment, the ohmic electrode of Example 1 was changed from Mo to Ti. When L was evaluated, it was confirmed that the TEM image contrast including InGaZnO was shorter than 200 nm by the oxygen removal of the Ti electrode, and the thickness of the semiconductor layer was 180 nm. Example 7 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-1. The results are disclosed in Table 2-1. Further, the semiconductor element of this embodiment satisfies the formula (I). In the embodiment, when Pd is sputtered when the Schottky electrode is fabricated, Ar and O are not used.2 The mixed gas was sputtered and only 70 Ar was used to form a film. As a result, at the InGaZnO/PdO interface, the peak from oxygen in the Pd spectrum of XPS from the InGaZnO/PdO interface is accompanied by a decrease in the oxygen concentration contained in InGaZnO, and it is impossible to determine that Pd contains oxygen. Further, in the region where Pd is observed by the EDX image, there is clearly no region where the contrast of the TEM image can be seen. Thus, it was judged that the Schottky electrode was a layer containing Pd of about 70 nm. As shown in Table 2-1, it is denoted as Pd. Example 8 An n-type Si substrate (4 inches in diameter and 250 μm in thickness) having a resistivity of 0.001 Ω·cm was mounted on a sputtering apparatus (manufactured by CANON ANELVA: E-200S), and a laminated electrode below the film was formed as an ohmic electrode layer. . However, for the reverse side of the substrate, Ti100 nm/Au50 nm treatment was performed in order to eliminate the contact resistance with the probe device during the measurement. First, 15 nm of Ti is formed in a DC50 W, Ar environment, and then 50 nm of Ni is formed in a DC 50 W, Ar environment. Finally, as a Schottky electrode, a film is formed in a DC 50 W, Ar environment. Mo of nm. Then, the substrate was placed in a sputtering apparatus (manufactured by ULVAC: CS-200) together with a semiconductor region mask, and InGaZnO (1:1:1) at 200 nm was formed as a withstand voltage layer (semiconductor layer). Film formation conditions are set to: DC300 W, Ar and H2 O mixed gas environment (H2 O concentration: 1% by volume). The sputtering target-substrate distance (TS interval) was set to 80 mm. The substrate was taken out and annealed in an electric furnace at 300 ° C for 1 hour in the air. The substrate and the electrode were again placed in a sputtering apparatus with a region mask (pore diameter: 50 μm), and a Pd target was placed in a mixed gas of argon gas and oxygen gas to form a 50 nm PdO as a Schottky electrode ( 50 μm in diameter). Thereafter, a Pd electrode of 100 μm was formed using the same mask. The film formation conditions were all set to DC100 W and Ar environment. As a final treatment, an under-tempering treatment at 200 ° C for 1 hour was carried out. Further, the element configuration is such that, as shown in FIG. 2, an ohmic electrode is provided on the lower portion of the semiconductor layer, and when the peripheral portion of the Schottky electrode is perpendicular to the ohmic electrode surface, the ohmic electrode surface is in the above-mentioned manner. The inside of the vertical line. The obtained semiconductor element was evaluated in the same manner as in Example 1. The results are disclosed in Table 2-1. Further, the semiconductor element of this embodiment satisfies the formula (I). Example 10 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-1. The results are disclosed in Table 2-1. Further, the semiconductor element of this embodiment satisfies the formula (I). In this example, the annealing temperature after film formation of the semiconductor layer was raised to 500 ° C, and as a result, it was found that the diffraction image at the time of cross-sectional TEM measurement was changed. The diffracted spot is wider but exists, and the spot position changes with respect to the measurement site of the complex point. From this, it was judged that the semiconductor film was polycrystalline. Further, it was observed that the thickness of the semiconductor layer also changed to 190 nm with crystallization. Example 11 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-2. The results are disclosed in Table 2-2. Further, the semiconductor element of this embodiment satisfies the formula (I). In this embodiment, the Schottky electrode uses Ru. The composition of Si/Ti/Ru/RuO/InGaZnO/Mo was formed. RuO is formed by sputtering using a mixed gas of Ar and oxygen. Example 12 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-2. The results are disclosed in Table 2-2. Further, the semiconductor element of this embodiment satisfies the formula (I). In this embodiment, the Schottky electrode uses Ni. A structure of Si/Ti/Ni/NiO/InGaZnO/Mo was formed. NiO is formed by sputtering using a mixed gas of Ar and oxygen. Example 13 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-2. The results are disclosed in Table 2-2. Further, the semiconductor element of this embodiment satisfies the formula (I). In this embodiment, the semiconductor layer was sputtered using an InSnZnO (1:1:1) target. Example 14 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-2. The results are disclosed in Table 2-2. Further, the semiconductor element of this embodiment satisfies the formula (I). Use Ga2 O3 The target sputters the semiconductor layer. Since it is an insulating sputtering target, it is DC300 W and uses RF (Radio Freqency) 300 W film forming conditions. Example 15 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-2. The results are disclosed in Table 2-2. Further, the semiconductor element of this embodiment satisfies the formula (I). In this embodiment, the environment in which the semiconductor layer was formed into a film was set to Ar 100% by volume, and the temperature at which the semiconductor was annealed was set to 150 ° C in the band. Use Ga2 O3 The target sputters the semiconductor layer. Since it is an insulating sputtering target, it becomes DC300 W and uses the film formation conditions of RF300W. Example 16 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-2. The results are disclosed in Table 2-2. Further, the semiconductor element of this embodiment satisfies the formula (I). In this embodiment, the semiconductor layer is sputtered using an InAlO (93:7) target. The obtained cross-sectional TEM measurement was found to change the diffraction image. The diffracted spot is wide but exists, and the position of the spot changes with respect to the measurement site of the complex point. However, even if a diffraction image was obtained in the film thickness direction, no change in the position of the light spot was observed. From this, it was judged that the semiconductor film was polycrystalline (columnar). Example 17 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-2. The results are disclosed in Table 2-2. Further, the semiconductor element of this embodiment satisfies the formula (I). In this embodiment, the semiconductor layer is sputtered using an InGaO (1:1) target. Further, in order to obtain crystallinity, the annealing temperature was raised to 600 °C. As a result, in the same manner as in the eighth embodiment, the PdO Schottky electrode was placed on the upper portion of the semiconductor layer as shown in FIG. The purpose is to reduce PdO to Pd by high temperature to suppress a decrease in Schottky barrier property. The obtained cross-sectional TEM measurement was found to change the diffraction image. The diffracted spot is wide but exists, and the position of the spot changes with respect to the measurement site of the complex point. However, even if a diffraction image was obtained in the film thickness direction, no change in the position of the light spot was observed. From this, it was judged that the semiconductor film was polycrystalline (columnar). Example 20 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 2-2. The results are disclosed in Table 2-2. In this embodiment, a configuration is provided in which a Schottky electrode is provided on the upper portion of the semiconductor layer as shown in FIG. 3, and an ohm is formed when the peripheral portion of the Schottky electrode is perpendicular to the ohmic electrode surface. The electrode faces are on the outer side of the above-mentioned vertical line. Although the formula (I) was satisfied, a decrease in withstand voltage and an increase in leakage current were observed as compared with Example 8. [table 2-1] [Table 2-2] Comparative Example 1 A semiconductor device was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 3. The results are revealed in 3. In this embodiment, the environment at the time of film formation of InGaZnO was set to Ar 100% by volume. Further, annealing after semiconductor film formation was not performed. As a result, the carrier concentration is outside the range of the formula (I). Moreover, the withstand voltage is also 0.1 MV/cm, which makes it difficult to adapt to power use characteristics. The leakage current is higher than the compliance current of the measuring device by 100 mA when -5 V is applied. It is impossible to make a measurement. Therefore, it is recorded as >1.0×10 in Table 3.-3 A. Comparative Example 2 A semiconductor device was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 3. The results are disclosed in Table 3. In this embodiment, the film formation of the Pd/PdO layer is omitted, and the Schottky electrode becomes Ti. As a result, although the rectification characteristics were observed, the carrier concentration became outside the range of the formula (I). Further, the leakage current is high and the withstand voltage is also 0.3 MV/cm, which makes it difficult to adapt to power use characteristics. Comparative Example 3 A semiconductor element was produced and evaluated in the same manner as in Example 1 except that the film formation conditions were changed as shown in Table 3. The results are disclosed in Table 3. In this embodiment, In is used2 O3 The target sputters the semiconductor layer. The obtained cross-sectional TEM measurement was found to change the diffraction image. The diffracted spot is wide but exists, and the position of the spot changes with respect to the measurement site of the complex point. However, even if a diffraction image was obtained in the film thickness direction, no change in the position of the light spot was observed. From this, it was judged that the semiconductor film was polycrystalline (columnar). Regarding the electrical characteristics, the carrier concentration was high, and the produced Schottky diode did not have a rectification ratio, and the carrier concentration could not be measured by CV measurement. Further, since the positive power is maintained at a value of 2 or less in the range of 2 to 3 V, the relationship of the judgment formula (5) is not satisfied, and the characteristic temperature cannot be evaluated. A decrease in withstand voltage and an increase in leakage current were observed. [table 3] [Industrial Applicability] The semiconductor element of the present invention can be used for a Schottky barrier diode and a junction transistor. Furthermore, these can be used in electronic circuits and used in various electric machines. The embodiments and/or the embodiments of the present invention are described in detail above, and the embodiments and/or embodiments of the present invention may be readily practiced without departing from the novel teachings and effects of the invention. Or the embodiment imposes a variety of changes. Accordingly, such various modifications are intended to be included within the scope of the present invention. The contents of the Japanese application form which is the basis of the priority of Paris in this case are all cited herein.

1‧‧‧半導體元件
2‧‧‧半導體元件
3‧‧‧半導體元件
4‧‧‧半導體元件
10‧‧‧肖特基電極
12‧‧‧肖特基電極之外周部
20‧‧‧歐姆電極
22‧‧‧歐姆電極面
30‧‧‧半導體層
40‧‧‧導電性基板
50‧‧‧絕緣層
60‧‧‧絕緣性基板
A‧‧‧垂線
1‧‧‧Semiconductor components
2‧‧‧Semiconductor components
3‧‧‧Semiconductor components
4‧‧‧Semiconductor components
10‧‧‧Schottky electrode
12‧‧‧Outside the Schottky electrode
20‧‧‧ Ohmic electrode
22‧‧‧Ohm electrode surface
30‧‧‧Semiconductor layer
40‧‧‧Electrically conductive substrate
50‧‧‧Insulation
60‧‧‧Insulating substrate
A‧‧‧ vertical line

圖1係本發明之一實施形態之半導體元件之概略剖視圖。 圖2係本發明之其他實施形態之半導體元件之概略剖視圖。 圖3係本發明之其他實施形態之半導體元件之概略立體圖。 圖4係本發明之其他實施形態之半導體元件之概略立體圖。 圖5係用於說明圖2之半導體元件之電極面之圖。BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a schematic cross-sectional view showing a semiconductor device according to an embodiment of the present invention. Fig. 2 is a schematic cross-sectional view showing a semiconductor device according to another embodiment of the present invention. Fig. 3 is a schematic perspective view showing a semiconductor device according to another embodiment of the present invention. Fig. 4 is a schematic perspective view showing a semiconductor device according to another embodiment of the present invention. Fig. 5 is a view for explaining an electrode surface of the semiconductor element of Fig. 2.

1‧‧‧半導體元件 1‧‧‧Semiconductor components

10‧‧‧肖特基電極 10‧‧‧Schottky electrode

20‧‧‧歐姆電極 20‧‧‧ Ohmic electrode

30‧‧‧半導體層 30‧‧‧Semiconductor layer

40‧‧‧導電性基板 40‧‧‧Electrically conductive substrate

Claims (16)

一種半導體元件,其特徵在於: 具有隔開之一對歐姆電極及肖特基電極、以及 與上述歐姆電極及上述肖特基電極相接之半導體層,且 滿足下述式(I): [數15](式中,n為上述半導體層之載子濃度(cm-3 ),ε為上述半導體層之介電常數(F/cm),Ve 為上述歐姆電極與上述肖特基電極之間之正向有效電壓(V),q為基本電荷(C),L為上述歐姆電極與上述肖特基電極之間之距離(cm))。A semiconductor device comprising: a pair of ohmic electrodes and a Schottky electrode; and a semiconductor layer connected to the ohmic electrode and the Schottky electrode, and satisfying the following formula (I): 15] (wherein n is a carrier concentration (cm -3 ) of the semiconductor layer, ε is a dielectric constant (F/cm) of the semiconductor layer, and Ve is a positive relationship between the ohmic electrode and the Schottky electrode To the effective voltage (V), q is the basic charge (C), and L is the distance (cm) between the above ohmic electrode and the above Schottky electrode. 如請求項1之半導體元件,其中上述半導體層包含金屬氧化物。The semiconductor device of claim 1, wherein the semiconductor layer comprises a metal oxide. 如請求項2之半導體元件,其中上述金屬氧化物含有選自In、Zn、Ga、Sn及Al中之一種以上之元素。The semiconductor device according to claim 2, wherein the metal oxide contains one or more elements selected from the group consisting of In, Zn, Ga, Sn, and Al. 如請求項1或2之半導體元件,其中上述肖特基電極包含選自Pd、Mo、Pt、Ir、Ru、W、Cr、Re、Te、Mn、Os、Fe、Rh、Co及Ni中之一種以上之金屬或其氧化物。The semiconductor device according to claim 1 or 2, wherein the Schottky electrode comprises one selected from the group consisting of Pd, Mo, Pt, Ir, Ru, W, Cr, Re, Te, Mn, Os, Fe, Rh, Co, and Ni. More than one metal or an oxide thereof. 如請求項1或2之半導體元件,其中上述歐姆電極包含選自Ti、Mo、Ag、In、Al、W、Co及Ni中之一種以上之金屬或其化合物。The semiconductor element according to claim 1 or 2, wherein the ohmic electrode comprises a metal selected from the group consisting of Ti, Mo, Ag, In, Al, W, Co, and Ni or a compound thereof. 如請求項1或2之半導體元件,其中上述半導體層包含非晶或多晶。The semiconductor element of claim 1 or 2, wherein the semiconductor layer comprises amorphous or polycrystalline. 如請求項1或2之半導體元件,其中上述半導體層之特性溫度為1500 K以下。The semiconductor element according to claim 1 or 2, wherein the semiconductor layer has a characteristic temperature of 1500 K or less. 如請求項1或2之半導體元件,其中於自肖特基電極之外周部向歐姆電極面劃垂線時,上述歐姆電極面處於上述垂線之內側。The semiconductor element according to claim 1 or 2, wherein the ohmic electrode surface is located inside the perpendicular line when the peripheral portion of the Schottky electrode is perpendicular to the ohmic electrode surface. 如請求項1或2之半導體元件,其耐壓為0.5 MV/cm以上。The semiconductor element of claim 1 or 2 has a withstand voltage of 0.5 MV/cm or more. 如請求項1或2之半導體元件,其中上述半導體層介於上述歐姆電極與上述肖特基電極之間。A semiconductor element according to claim 1 or 2, wherein said semiconductor layer is interposed between said ohmic electrode and said Schottky electrode. 如請求項10之半導體元件,其進而具有導電性矽基板,且 上述歐姆電極或上述肖特基電極與上述導電性矽基板相接。The semiconductor device of claim 10, further comprising a conductive germanium substrate, wherein the ohmic electrode or the Schottky electrode is in contact with the conductive germanium substrate. 如請求項1或2之半導體元件,其中上述歐姆電極與上述肖特基電極隔開間隔地存在於上述半導體層之一表面上。A semiconductor element according to claim 1 or 2, wherein said ohmic electrode is present on a surface of said one of said semiconductor layers at a distance from said Schottky electrode. 一種肖特基能障二極體,其特徵在於:使用如請求項1至12中任一項之半導體元件。A Schottky barrier diode characterized by using the semiconductor device according to any one of claims 1 to 12. 一種接面電晶體,其特徵在於:使用如請求項1至12中任一項之半導體元件。A junction transistor characterized by using the semiconductor element according to any one of claims 1 to 12. 一種電子電路,其特徵在於:使用如請求項1至12中任一項之半導體元件、如請求項13之肖特基能障二極體或如請求項14之接面電晶體。An electronic circuit characterized by using a semiconductor element according to any one of claims 1 to 12, a Schottky barrier diode of claim 13, or a junction transistor as claimed in claim 14. 一種電氣機器、電子機器、車輛或動力機構,其特徵在於:使用如請求項15之電子電路。An electrical machine, an electronic machine, a vehicle or a power mechanism, characterized in that an electronic circuit as claimed in claim 15 is used.
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