TWI742828B - Gallium nitride epitaxial wafer capable of reducing stress - Google Patents
Gallium nitride epitaxial wafer capable of reducing stress Download PDFInfo
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- 229910002601 GaN Inorganic materials 0.000 title claims abstract description 190
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 title claims abstract description 71
- RNQKDQAVIXDKAG-UHFFFAOYSA-N aluminum gallium Chemical compound [Al].[Ga] RNQKDQAVIXDKAG-UHFFFAOYSA-N 0.000 claims abstract description 123
- 230000006911 nucleation Effects 0.000 claims abstract description 43
- 238000010899 nucleation Methods 0.000 claims abstract description 43
- 239000000758 substrate Substances 0.000 claims abstract description 32
- 239000002019 doping agent Substances 0.000 claims description 28
- 239000000463 material Substances 0.000 claims description 20
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 18
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 16
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 claims description 16
- 229910052710 silicon Inorganic materials 0.000 claims description 16
- 239000010703 silicon Substances 0.000 claims description 16
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 12
- 229910052782 aluminium Inorganic materials 0.000 claims description 11
- 238000000407 epitaxy Methods 0.000 claims description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 6
- 229910052749 magnesium Inorganic materials 0.000 claims description 6
- 239000011777 magnesium Substances 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 229910052733 gallium Inorganic materials 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- 239000011701 zinc Substances 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- 229910052594 sapphire Inorganic materials 0.000 claims description 3
- 239000010980 sapphire Substances 0.000 claims description 3
- 150000004767 nitrides Chemical class 0.000 claims description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 2
- 230000012010 growth Effects 0.000 description 23
- 238000000034 method Methods 0.000 description 12
- 239000012212 insulator Substances 0.000 description 7
- 150000002500 ions Chemical class 0.000 description 7
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 239000013078 crystal Substances 0.000 description 6
- 239000004065 semiconductor Substances 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 5
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- 238000009826 distribution Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 230000005533 two-dimensional electron gas Effects 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- 229910000577 Silicon-germanium Inorganic materials 0.000 description 1
- LEVVHYCKPQWKOP-UHFFFAOYSA-N [Si].[Ge] Chemical compound [Si].[Ge] LEVVHYCKPQWKOP-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
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- 239000000969 carrier Substances 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
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- 230000005684 electric field Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 230000007773 growth pattern Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
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- 238000012545 processing Methods 0.000 description 1
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Abstract
Description
本發明大體上與一種氮化鎵磊晶片有關,更具體言之,其係關於一種成長在絕緣層上覆矽晶圓(silicon-on-insulator,SOI)上、可降低成長應力的氮化鎵磊晶片。 The present invention is generally related to a gallium nitride epitaxial wafer, and more specifically, it relates to a gallium nitride grown on a silicon-on-insulator (SOI) wafer that can reduce growth stress. Epi wafer.
近幾年氮化鎵(GaN)材料在業界受到多方面的關注及應用,如未來5G市場、電動車、雷達衛星通訊、無線電傳輸以及醫療技術。因為氮化鎵材料具有高能帶、高擊穿電場、高導熱率、高飽和電子速度以及元件體積小等特性,這些特性使得氮化鎵在高功率及高速電晶體管的應用上被視為是相當理想的材料,尤其是在高頻元件的應用上相當廣泛。 In recent years, gallium nitride (GaN) materials have received many attentions and applications in the industry, such as the future 5G market, electric vehicles, radar satellite communications, radio transmission, and medical technology. Because gallium nitride material has the characteristics of high energy band, high breakdown electric field, high thermal conductivity, high saturated electron velocity and small component size, these characteristics make gallium nitride regarded as equivalent in the application of high power and high speed electrical transistors. Ideal material, especially in the application of high-frequency components is quite extensive.
矽基板在價格成本上有其競爭優勢,因此將氮化鎵生長在矽基板上的電路設計方案正在蓬勃地研究與發展。然而,氮化鎵與矽基板在先天上的晶格常數與熱膨脹係數等性質差異過大,如此將氮化鎵直接成長在矽基板上的異質磊晶方式會造成過大的晶格失配(約17%)及熱膨脹係數失配(約54%),成長期間會產生很大的拉應力,形成高密度的螺旋錯位,進而使晶圓翹曲甚至產生裂紋,如此在電性方面會導致所形成的氮化鎵元件漏電流增加並降低載子遷移率與運作效率。 Silicon substrates have competitive advantages in terms of price and cost. Therefore, circuit design schemes for growing gallium nitride on silicon substrates are being researched and developed vigorously. However, the inherent lattice constants and thermal expansion coefficients of gallium nitride and silicon substrates are too different in nature, so the heteroepitaxial method of directly growing gallium nitride on silicon substrates will cause excessive lattice mismatch (about 17 %) and thermal expansion coefficient mismatch (approximately 54%). During the growth period, a large tensile stress will be generated, forming a high-density spiral dislocation, which will cause the wafer to warp or even crack, which will lead to the formation of electrical Gallium nitride devices increase leakage current and reduce carrier mobility and operating efficiency.
目前業界已提出有數種方法來解決上述氮化鎵與矽基板不匹配的問 題,其中一種方法是將氮化鎵成長在絕緣層上覆矽晶圓(silicon-on-insulator,SOI)之上。 At present, the industry has proposed several methods to solve the above-mentioned problem of the mismatch between gallium nitride and silicon substrates. Question, one of the methods is to grow gallium nitride on a silicon-on-insulator (SOI) wafer.
有鑑於上述氮化鎵成長的習知問題,本發明基於現有業界所提出的解決方案,提出了一種改良的、具有高品質與低損耗特性的氮化鎵磊晶片,其透過將氮化鎵成長在絕緣層上覆矽晶圓(silicon-on-insulator,SOI),並搭配漸變層以及中間層超晶格結構(inter super lattices structure,inter-SLS)的變化來緩衝氮化鎵成長時所帶來的應力,並使得整體磊晶結構的厚度可超過10um,崩潰電壓可超過1000伏特,如此提升了氮化鎵元件的效率,其特別適合用來製作氮化鎵系的高電子遷移率電晶體(high electron mobility transistors,HEMTs)。 In view of the above-mentioned conventional problems in the growth of gallium nitride, the present invention proposes an improved gallium nitride epitaxial wafer with high quality and low loss characteristics based on the existing solutions proposed in the industry. Overlay a silicon-on-insulator (SOI) on the insulating layer, and match the graded layer and the change of the inter super lattices structure (inter-SLS) to buffer the growth of gallium nitride The stress caused by the overall epitaxial structure can exceed 10um, and the breakdown voltage can exceed 1000 volts. This improves the efficiency of gallium nitride devices. It is particularly suitable for making gallium nitride-based high electron mobility transistors. (high electron mobility transistors, HEMTs).
本發明的目的為提出一種可降低應力的氮化鎵磊晶片,包含一基板、一成核層位在該基板上、多個氮化鋁鎵緩衝層位在該成核層上、多個中間超晶格結構層,其中部分的該中間超晶格結構層位於兩個該氮化鋁鎵緩衝層之間、一高阻值層,位在最上層的該氮化鋁鎵緩衝層上、一本質氮化鎵層,位在該高阻值層上、一電子提供層位在該本質氮化鎵層上、以及一覆蓋層,位在該電子提供層上。 The purpose of the present invention is to provide a gallium nitride epitaxial wafer capable of reducing stress, comprising a substrate, a nucleation layer on the substrate, a plurality of aluminum gallium nitride buffer layers on the nucleation layer, and a plurality of intermediate layers. Superlattice structure layer, in which part of the intermediate superlattice structure layer is located between the two aluminum gallium nitride buffer layers, a high resistance layer, is located on the uppermost aluminum gallium nitride buffer layer, and The essential gallium nitride layer is located on the high resistance layer, an electron supply layer is located on the essential gallium nitride layer, and a covering layer is located on the electron supply layer.
本發明的這類目的與其他目的在閱者讀過下文中以多種圖示與繪圖來描述的較佳實施例之細節說明後應可變得更為明瞭顯見。 Such objects and other objects of the present invention should become more apparent after readers have read the detailed description of the preferred embodiments described below with various illustrations and drawings.
100:支撐晶圓 100: Support wafer
101:絕緣氧化層 101: insulating oxide layer
103:元件晶圓 103: Component Wafer
110:基板(絕緣層上覆矽晶圓) 110: Substrate (silicon wafer over insulating layer)
120:成核層 120: Nucleation layer
121:低溫氮化鋁層 121: low temperature aluminum nitride layer
122:高溫氮化鋁層 122: high temperature aluminum nitride layer
130:中間超晶格結構層 130: Intermediate superlattice structure layer
130a,130b,130c:超晶格組 130a, 130b, 130c: superlattice group
140:超晶格對 140: Superlattice Pair
140a:第一超晶格層 140a: the first superlattice layer
140b:第二超晶格層 140b: second superlattice layer
150:緩衝層 150: buffer layer
151:(第一)氮化鋁鎵緩衝層 151: (first) aluminum gallium nitride buffer layer
152:(第二)氮化鋁鎵緩衝層 152: (Second) Aluminum Gallium Nitride buffer layer
153:(第三)氮化鋁鎵緩衝層 153: (third) aluminum gallium nitride buffer layer
154:(第四)氮化鋁鎵緩衝層 154: (fourth) aluminum gallium nitride buffer layer
155:(第五)氮化鋁鎵緩衝層 155: (fifth) aluminum gallium nitride buffer layer
160:高阻值層 160: high resistance layer
170:本質氮化鎵層 170: Intrinsic GaN layer
180:電子提供層 180: electronic provision layer
190:覆蓋層 190: Overlay
本說明書含有附圖併於文中構成了本說明書之一部分,俾使閱者對本發明實施例有進一步的瞭解。該些圖示係描繪了本發明一些實施例並連同本文描述 一起說明了其原理。在該些圖示中:第1圖繪示出根據本發明實施例中一絕緣層上覆矽(silicon-on-insulator,SOI)晶圓的製作流程;第2圖繪示出根據本發明實施例中在絕緣層上覆矽晶圓上形成成核層的步驟;第3圖繪示出根據本發明較佳實施例中一中間超晶格結構層的細部結構;第4圖繪示出根據本發明一實施例中緩衝層形成在成核層上的型態;第5圖繪示出根據本發明另一實施例中緩衝層形成在成核層上的型態;第6圖繪示出根據本發明又一實施例中緩衝層形成在成核層上的型態;第7圖繪示出根據本發明又一實施例中緩衝層形成在成核層上的型態;第8圖繪示出根據本發明又一實施例中緩衝層形成在成核層上的型態;第9圖繪示出根據本發明又一實施例中緩衝層形成在成核層上的型態;以及第10圖繪示出根據本發明較佳實施例中一氮化鎵磊晶片的細部結構。 This specification contains drawings and constitutes a part of this specification in the text, so that readers can have a further understanding of the embodiments of the present invention. These diagrams depict some embodiments of the invention and are described herein together The principle is explained together. In these figures: Figure 1 illustrates the manufacturing process of a silicon-on-insulator (SOI) wafer according to an embodiment of the present invention; Figure 2 illustrates an implementation according to the present invention In the example, the step of forming a nucleation layer on a silicon wafer over an insulating layer; Fig. 3 illustrates the detailed structure of an intermediate superlattice structure layer in a preferred embodiment of the present invention; Fig. 4 illustrates a step according to The type of buffer layer formed on the nucleation layer in an embodiment of the present invention; FIG. 5 illustrates the type of buffer layer formed on the nucleation layer in another embodiment of the present invention; FIG. 6 illustrates According to another embodiment of the present invention, the buffer layer is formed on the nucleation layer; Fig. 7 shows the buffer layer formed on the nucleation layer in another embodiment of the present invention; Fig. 8 is Figure 9 illustrates the form of the buffer layer formed on the nucleation layer according to another embodiment of the present invention; Figure 9 depicts the form of the buffer layer formed on the nucleation layer according to another embodiment of the present invention; and Figure 10 illustrates the detailed structure of a gallium nitride epitaxial wafer according to a preferred embodiment of the present invention.
須注意本說明書中的所有圖示皆為圖例性質,為了清楚與方便圖示說明之故,圖示中的各部件在尺寸與比例上可能會被誇大或縮小地呈現,一般而言,圖中相同的參考符號會用來標示修改後或不同實施例中對應或類似的元件特徵。 It should be noted that all the illustrations in this manual are illustrations in nature. For clarity and convenience of illustration, the parts in the illustrations may be exaggerated or reduced in size and proportion. Generally speaking, the figures The same reference symbols will be used to indicate corresponding or similar element features in modified or different embodiments.
現在下文將詳細說明本發明的示例性實施例,其會參照附圖示出所描述之特徵以便閱者理解並實現技術效果。閱者將可理解文中之描述僅透過例示之方式來進行,而非意欲要限制本案。本案的各種實施例和實施例中彼此不衝突的各種特徵可以以各種方式來加以組合或重新設置。在不脫離本發明的精神與範疇的情況下,對本案的修改、等同物或改進對於本領域技術人員來說是 可以理解的,並且旨在包含在本案的範圍內。 Now, exemplary embodiments of the present invention will be described in detail below, which will illustrate the described features with reference to the accompanying drawings so that readers can understand and achieve technical effects. Readers will understand that the description in the text is only done by way of example, and is not intended to limit the case. The various embodiments of this case and various features in the embodiments that do not conflict with each other can be combined or re-arranged in various ways. Without departing from the spirit and scope of the present invention, modifications, equivalents or improvements to this case are for those skilled in the art It is understandable and intended to be included in the scope of this case.
閱者應能容易理解,本案中的「在…上」、「在…之上」和「在…上方」的含義應當以廣義的方式被解讀,以使得「在…上」不僅表示「直接在」某物「上」,而且還包括在某物「上」且其間有居間特徵或層的含義,並且「在…之上」或「在…上方」不僅表示「在」某物「之上」或「上方」的含義,而且還可以包括其「在」某物「之上」或「上方」且其間沒有居間特徵或層(即,直接在某物上)的含義。 Readers should be able to easily understand that the meanings of "on", "on" and "on" in this case should be interpreted in a broad way, so that "on" not only means "directly on" "Something is "on", but also includes "on" something with the meaning of intervening features or layers in between, and "on" or "on" not only means "on" something "on" Or "above", and it can also include the meaning of "above" or "above" something without intervening features or layers (that is, directly on something).
此外,為了描述方便,諸如「在…之下」、「在…下方」、「下部」、「在…之上」、「上部」等空間相關的術語在本文中可以用於描述一個元件或特徵與另一個或多個元件或特徵之間的關係,如在附圖中示出的。 In addition, for the convenience of description, space-related terms such as "below", "below", "lower", "above", "upper" and other space-related terms can be used herein to describe an element or feature The relationship with another element or features is as shown in the drawings.
在下文的描述中,「基底」與「晶圓」兩詞是可以互換的,其可包含內部中或表面上有電路形成的任何半導體結構。這些結構可包含矽、覆矽絕緣基底(SOI)、覆矽藍寶石基底(SOS)、摻雜或未摻雜的半導體、被半導體基材所支撐的矽質磊晶層、或是其他半導體結構等。半導體不一定要矽質的,其也可為矽鍺、鍺、或是砷化鎵。當下文中提到基底時,其半導體基材中或上方可能已經有進行過製程步驟而形成層、區域或接面等結構。 In the following description, the terms "substrate" and "wafer" are interchangeable, and can include any semiconductor structure with circuits formed inside or on the surface. These structures can include silicon, silicon-on-insulator (SOI), silicon-on-sapphire (SOS), doped or undoped semiconductors, silicon epitaxial layers supported by semiconductor substrates, or other semiconductor structures, etc. . The semiconductor does not have to be silicon, it can also be silicon germanium, germanium, or gallium arsenide. When the substrate is mentioned in the following, there may have been processing steps in or on the semiconductor substrate to form a layer, region, or junction structure.
如本文中使用的,術語「層」是指包括具有厚度區域的材料部分。層可以在下方或上方結構的整體之上延伸,或者可以具有小於下方或上方結構範圍的範圍。此外,層可以是厚度小於連續結構的厚度的均質或非均質連續結構的區域。例如,層可以位於在連續結構的頂表面和底表面之間或在頂表面和底表面處的任何水平面對之間。層可以水準、豎直和/或沿傾斜表面延伸。基底可以是層,其中可以包括一個或多個層,和/或可以在其上、其上方和/或其下方具有一個或多個層。 As used herein, the term "layer" refers to a portion of material that includes regions of thickness. The layer may extend over the entirety of the lower or upper structure, or may have a range smaller than the range of the lower or upper structure. In addition, the layer may be a region of a homogeneous or non-homogeneous continuous structure whose thickness is less than that of the continuous structure. For example, the layer may be located between the top and bottom surfaces of the continuous structure or between any horizontal faces at the top and bottom surfaces. The layers can extend horizontally, vertically, and/or along inclined surfaces. The substrate may be a layer, which may include one or more layers, and/or may have one or more layers on, above, and/or below it.
文中描述會使用「N」與「P」等稱號,一般以「N型」與「P型」的 方式,來指稱會促發電子與電洞作為主要載體的施體與受體類摻質。一個摻質類型後綴有「++」符號代表了其摻雜濃度是高於那些後綴為「+」符號的摻質的摻雜濃度。反之,後綴為「-」符號的摻質類型代表了其摻質的摻雜濃度是低於那些沒有後綴符號的摻質的摻雜濃度。 The description in the text will use names such as "N" and "P", generally with "N-type" and "P-type" It refers to the donor and acceptor dopants that promote electrons and holes as the main carriers. A dopant type suffixed with a "++" symbol indicates that its doping concentration is higher than that of those dopants suffixed with a "+" symbol. Conversely, the dopant type with the suffix "-" means that the dopant concentration of the dopant is lower than the dopant concentration of the dopants without the suffix symbol.
首先請參照第1圖,其繪示出根據本發明實施例中一絕緣層上覆矽(silicon-on-insulator,SOI)晶圓的製作流程。首先提供一片支撐晶圓(handle wafer)100,其較佳為重摻雜矽晶圓,也可使用硬度較大的碳化矽晶圓或是藍寶石晶圓等,其厚度約在300~800um之間。接著,對支撐晶圓100進行高溫氧化製程,使得其雙面上成長出絕緣氧化層101。高溫氧化製程期間的溫度可介於1000~1100℃,所成長出的絕緣氧化層101的厚度介於0.05~5um,其材料視來源的支撐晶圓100而定可為氧化矽(SiO2)或氧化鋁(Al2O3)。接著,將一片元件晶圓(device wafer)103鍵合到支撐晶圓100其中一面的絕緣氧化層101上並進行退火製程,使得兩者間的弱鍵結轉化為共價鍵堅固的接合狀態。最後,將接合後的元件晶圓103利用化學機械研磨(CMP)或是晶背研磨等製程減薄至所需厚度,約1~10um之間,如此即完成了一絕緣層上覆矽晶圓110。
Firstly, please refer to FIG. 1, which illustrates the manufacturing process of a silicon-on-insulator (SOI) wafer according to an embodiment of the present invention. First, a
上述實施例中所形成的絕緣層上覆矽晶圓110將在後續實施例中作為本發明氮化鎵磊晶片的基底。其中,絕緣層上覆矽晶圓110中與元件晶圓103相接的絕緣氧化層101係可作為矽電晶體之間的絕緣體物質,可大量降低其間的寄生電容,另一面的絕緣氧化層101則可做為一固定層來補償後續磊晶製程期間所產生的應力,避免晶圓產生習知的翹曲問題。
The silicon-on-insulating
完成絕緣層上覆矽晶圓110的製備後,接下來即是進行本發明氮化鎵磊晶片的製作。為了要在絕緣層上覆矽晶圓110上成長異質磊晶,需要先在絕緣層上覆矽晶圓110上形成成核層與緩衝層,以確保所生長出的磊晶的品質。本發明較佳實施例採用雙層不同性質的成核層,首先,利用有機金屬化學氣相沉積
法(MOCVD)在絕緣層上覆矽晶圓110上先成長一低溫氮化鋁層(LT-AlN)121,其成長溫度介於900~1000℃,厚度則介於30~80nm之間。之後,在低溫氮化鋁層121上成長一高溫氮化鋁層(HT-AlN)122,其成長溫度介於1000~1300℃,厚度介於30~200nm之間。透過在成長氮化鎵磊晶層前先成長低溫/高溫兩種不同性質的氮化鋁成核層,後續的氮化鎵磊晶層的成長會趨於二維成長態樣,會具有較為平坦的表面以及較好的晶體品質。後文的實施例中將以成核層120來統稱低溫氮化鋁層121與高溫氮化鋁層122。
After completing the preparation of the silicon-on-
完成了成核層120之製作後,接下來要進行緩衝層的製作。本發明的一大特點為,緩衝層是由多個漸變層與穿插在其間的一或多個中間超晶格結構(inter-superlattice structure,inter-SLS)層所構成的。其中,在本發明實施例中,該多個漸變層可為氮化鋁鎵(AlxGa(1-x)N)緩衝層,其各個氮化鋁鎵緩衝層中的鋁原子比例彼此不同,且每個單一氮化鋁鎵緩衝層中的鋁原子比例也呈漸變而非固定型態。另一方面,本發明的中間超晶格結構層是由兩種或多種材料所構成的周期性交替疊層結構,其設置在漸變緩衝層之間將有助於將兩側的晶格連在一起而不產生界面失配錯位,使晶格完全處於彈性應變狀態。
After the production of the
現在請參照第3圖,其繪示出了本發明實施例中一中間超晶格結構層130的細部結構。在本發明中,每一個中間超晶格結構層130都是由多個超晶格組以層疊方式所組成,該多個超晶格組具有相同的材料組成,但是具有不同的厚度分布。本發明實施例中,中間超晶格結構層130內的超晶格組較佳為三組,在圖中以130a,130b,130c來代表。再者,每個超晶格組130a,130b,130c還進一步包含多個超晶格對。例如,在較佳實施例中,每個超晶格組130a,130b,130c具有40個超晶格對,在圖中以140來代表一個超晶格對,同一個超晶格組中的多個超晶格對140可具有完全相同的結構與材料組成。再者,每個超晶格對140還進一步包含一第一超晶格層140a以及位於第一超晶格層140a上的第二超晶格層140b。第一
超晶格層140a與第二超晶格層140b具有相同的材料組成,但是具有不同的原子比例以及厚度分布。
Please refer now to FIG. 3, which illustrates the detailed structure of an intermediate
現在將以實際數據來說明中間超晶格結構層130、超晶格組130a,130b,130c、超晶格對140、第一超晶格層140a以及第二超晶格層140b的細部特徵。在本發明較佳實施例中,一個中間超晶格結構層130共分為三個超晶格組130a,130b,130c,每個超晶格組130a,130b,130c進一步分為40個超晶格對140,故一個中間超晶格結構層130共有120個超晶格對140,其中第1-40對為第一組,第41-80對為第二組,第81-120對為第三組。其中,這三個超晶格組130a,130b,130c中的超晶格對140的組成都相同,每個超晶格對140都是由一第一超晶格層140a與一第二超晶格層140b組成。第一超晶格層140a與一第二超晶格層140b的材料可為氮化鋁鎵,但是兩者具有不同的鋁原子比例,例如第一超晶格層140a為AlxGa(1-x)N而第二超晶格層140b為AlyGa(1-y)N,其中x不等於y。再者,不同超晶格組130a,130b,130c中的超晶格對140的第一超晶格層140a與第二超晶格層140b會具有不同的厚度。例如第一超晶格組130a中的超晶格對140(第1-40對)的第一超晶格層140a與第二超晶格層140b的厚度的分布範圍分別為21~25nm/1~6nm,第二超晶格組130b中的超晶格對140(第41-80對)的第一超晶格層140a與第二超晶格層140b的厚度的分布範圍分別為11~15nm/11~15nm,第三超晶格組130c中的超晶格對140(第81-120對)的第一超晶格層140a與第二超晶格層140b的厚度的分布範圍分別為1~6nm/21~25nm,可以看出離基板110越遠(即越上層的)的超晶格組中的第一超晶格層140a的厚度會越小,離基板110越遠的超晶格組中的第二超晶格層140b的厚度越大。上述的超晶格層都可以透過MOCVD方式來成長形成,其成長溫度介於950~1150℃。此外,第一超晶格層140a與第二超晶格層140b的鋁原子比例將由其中間超晶格結構層130上下所連接的層結構中的鋁原子比例相同,其在後續實施例中將有進一步的說明。
The detailed characteristics of the intermediate
本發明上述的中間超晶格結構層130可以多種形式穿插在緩衝層的各層結構之間來達成所需功效,以下將以不同的實施例來說明:
The above-mentioned intermediate
[實施例1] [Example 1]
請參照第4圖,其繪示出根據本發明一實施例中一緩衝層150形成在成核層120上的型態。在此實施例中,緩衝層150共包含五個氮化鋁鎵緩衝層(漸變層)151-155以及一個中間超晶格結構層130,其中中間超晶格結構層130係設置在成核層120與最下層的氮化鋁鎵緩衝層151之間。在結構成分方面,五個氮化鋁鎵緩衝層151-155的成分雖然都是氮化鋁鎵(AlzGa(1-2)N),但是其鋁原子的比例卻不相同。例如在實施例中,第一氮化鋁鎵緩衝層151的z介於0.7~0.95之間,第二氮化鋁鎵緩衝層152的z介於0.5~0.65之間,第三氮化鋁鎵緩衝層153的z介於0.3-0.45之間,第四氮化鋁鎵緩衝層154的z介於0.15-0.25之間,第五氮化鋁鎵緩衝層155的z介於0.05-0.15之間。可以看出在本發明實施例中,離基板110越遠、越靠上層的氮化鋁鎵緩衝層151-155,其設定的鋁原子比例越低。如此越靠上層鋁原子比例越低的氮化鋁鎵緩衝層之設計可以有效緩衝從氮化鋁材質的成核層120到後續所要成長的氮化鎵磊晶層的應力。另一方面,在本發明實施例中,單一氮化鋁鎵緩衝層中的鋁原子比例也可呈漸變型態,例如以第一氮化鋁鎵緩衝層151為例,其AlzGa(1-z)N成分中的z值(鋁原子比例)介於0.7~0.95之間,其可能是第一氮化鋁鎵緩衝層151中的z值從靠近基板110一側的0.95往遠離基板110一側的0.7逐漸變小。此氮化鋁鎵緩衝層中鋁原子比例漸變型態的設計亦有助於應力的逐步緩衝。上述的各氮化鋁鎵緩衝層151-155都可以透過MOCVD方式來成長形成,其成長溫度介於1000~1200℃。
Please refer to FIG. 4, which illustrates a type of a
除了鋁原子比例的變化,在本發明實施例中,各個氮化鋁鎵緩衝層151-155的厚度也有所不同。基本上,離基板110越遠的氮化鋁鎵緩衝層151-155
的厚度就越大。例如,在本發明實施例中,第一氮化鋁鎵緩衝層151的厚度介於50~200nm之間,第二氮化鋁鎵緩衝層152的厚度介於150~220nm之間,第三氮化鋁鎵緩衝層153的厚度介於350~600nm之間,第四氮化鋁鎵緩衝層151的厚度介於800~1500nm之間,第五氮化鋁鎵緩衝層155的厚度介於1600~2300nm之間。如此越往上層氮化鋁鎵緩衝層的厚度越厚的設計亦可有效緩解後續氮化鎵成長時的應力影響。
In addition to the change in the aluminum atomic ratio, in the embodiment of the present invention, the thickness of each aluminum gallium nitride buffer layer 151-155 is also different. Basically, the aluminum gallium nitride buffer layer 151-155 farther away from the
再者,在本發明實施例中,氮化鋁鎵緩衝層151-155中還可以摻入雜質,例如摻入碳、鐵、鎂以及鋅等或其組合的摻質,使得氮化鋁鎵緩衝層151-155變為摻雜氮化鋁鎵層。其中,所摻入的摻質濃度也會因各氮化鋁鎵緩衝層151-155而有所不同。例如,在本發明實施例中,第一氮化鋁鎵緩衝層151的摻質濃度大於1x1017離子/立方公分,第二氮化鋁鎵緩衝層152的摻質濃度大於3x1017離子/立方公分,第三氮化鋁鎵緩衝層153的摻質濃度大於5x1017離子/立方公分,第四氮化鋁鎵緩衝層154的摻質濃度大於7x1017離子/立方公分,第五氮化鋁鎵緩衝層155的摻質濃度大於1x1018離子/立方公分。可以看出越往上層的氮化鋁鎵緩衝層,其摻質濃度越大。此摻值濃度的漸變設計亦有助於電性的提升。
Furthermore, in the embodiment of the present invention, the aluminum gallium nitride buffer layer 151-155 may also be doped with impurities, such as doped with dopants of carbon, iron, magnesium, zinc, etc. or a combination thereof, so that the aluminum gallium nitride buffer layer Layers 151-155 become doped aluminum gallium nitride layers. Wherein, the dopant concentration doped will also be different for each aluminum gallium nitride buffer layer 151-155. For example, in the embodiment of the present invention, the dopant concentration of the first aluminum gallium
關於在本實施例中,設置在成核層120與第一氮化鋁鎵緩衝層151之間的中間超晶格結構層130,前文中曾提到中間超晶格結構層130中的第一超晶格層140a與第二超晶格層140b的鋁原子比例將由其中間超晶格結構層130上下所連接的層結構中的鋁原子比例相同。以本實施例為例,中間超晶格結構層130的第一超晶格層140a會連接到下方的成核層120,在成核層120的材料為氮化鋁的基礎上,其氮化鋁鎵(AlxGa(1-x)N)材質的第一超晶格層140a中的鋁原子比例x較佳為接近或等於1。中間超晶格結構層130的第二超晶格層140b會連接到上方的第一氮化鋁鎵緩衝層151,在前述第一氮化鋁鎵緩衝層151的材料為氮化鋁鎵的基礎上(AlzGa(1-z)N,其z值介於0.7~0.95之間),同為氮化鋁鎵(AlxGa(1-x)N)材質的第二超晶
格層140b中的鋁原子比例x較佳也在0.7~0.95之間。以如此設置,穿插在緩衝層結構中的中間超晶格結構層130能藉由其多個超薄且具有與上下兩接面相同成分組成的超晶格對140的周期性交替疊層設置來達成將兩側的晶格連在一起而不產生介面失配錯位的功效。
Regarding the intermediate
[實施例2] [Example 2]
請參照第5圖,其繪示出根據本發明另一實施例中緩衝層150形成在成核層120上的型態。此實施例設計將兩個中間超晶格結構層130插入任意的氮化鋁鎵緩衝層151-155之間(包含最下方的成核層120),如此可有共15種的插入組合。以圖中為例,成核層120與第一氮化鋁鎵緩衝層151之間以及第一氮化鋁鎵緩衝層151與第二氮化鋁鎵緩衝層152之間插入有中間超晶格結構層130。其他關於緩衝層150中的氮化鋁鎵緩衝層151-155以及中間超晶格結構層130的成分、鋁原子比例、厚度、摻質濃度以及成長方式等規則與實施例1相同。
Please refer to FIG. 5, which illustrates a type of the
[實施例3] [Example 3]
請參照第6圖,其繪示出根據本發明又一實施例中緩衝層150形成在成核層120上的型態。此實施例設計將三個中間超晶格結構層130插入任意的氮化鋁鎵緩衝層151-155之間(包含最下方的成核層120),如此可有共20種的插入組合。以圖中為例,成核層120與第一氮化鋁鎵緩衝層151之間、第一氮化鋁鎵緩衝層151與第二氮化鋁鎵緩衝層152之間、以及第二氮化鋁鎵緩衝層152與第三氮化鋁鎵緩衝層153之間插入有中間超晶格結構層130。其他關於緩衝層150中的氮化鋁鎵緩衝層151-155以及中間超晶格結構層130的成分、鋁原子比例、厚度、摻質濃度以及成長方式等規則與實施例1相同。
Please refer to FIG. 6, which depicts a pattern of the
[實施例4] [Example 4]
請參照第7圖,其繪示出根據本發明又一實施例中緩衝層150形成在成核層120上的型態。此實施例設計將四個中間超晶格結構層130插入任意的氮化鋁鎵緩衝層151-155之間(包含最下方的成核層120),如此可有共15種的插入組合。以圖中為例,成核層120與第一氮化鋁鎵緩衝層151之間、第一氮化鋁鎵緩衝層151與第二氮化鋁鎵緩衝層152之間、第二氮化鋁鎵緩衝層152與第三氮化鋁鎵緩衝層153之間、以及第三氮化鋁鎵緩衝層153與第四氮化鋁鎵緩衝層154之間插入有中間超晶格結構層130。其他關於緩衝層150中的氮化鋁鎵緩衝層151-155以及中間超晶格結構層130的成分、鋁原子比例、厚度、摻質濃度以及成長方式等規則與實施例1相同。
Please refer to FIG. 7, which illustrates the type of the
[實施例5] [Example 5]
請參照第8圖,其繪示出根據本發明又一實施例中緩衝層150形成在成核層120上的型態。此實施例設計將五個中間超晶格結構層130插入任意的氮化鋁鎵緩衝層151-155之間(包含最下方的成核層120),如此可有共6種的插入組合。以圖中為例,成核層120與第一氮化鋁鎵緩衝層151之間、第一氮化鋁鎵緩衝層151與第二氮化鋁鎵緩衝層152之間、第二氮化鋁鎵緩衝層152與第三氮化鋁鎵緩衝層153之間、第三氮化鋁鎵緩衝層153與第四氮化鋁鎵緩衝層154之間、以及第四氮化鋁鎵緩衝層154與第五氮化鋁鎵緩衝層155之間插入有中間超晶格結構層130。其他關於緩衝層150中的氮化鋁鎵緩衝層151-155以及中間超晶格結構層130的成分、鋁原子比例、厚度、摻質濃度以及成長方式等規則與實施例1相同。
Please refer to FIG. 8, which illustrates the type of the
[實施例6] [Example 6]
請參照第9圖,其繪示出根據本發明又一實施例中緩衝層150形成在
成核層120上的型態。此實施例設計將六個中間超晶格結構層130插入任意的氮化鋁鎵緩衝層151-155之間(包含最下方的成核層120),如此可有共1種的插入組合。以圖中為例,成核層120與第一氮化鋁鎵緩衝層151之間、第一氮化鋁鎵緩衝層151與第二氮化鋁鎵緩衝層152之間、第二氮化鋁鎵緩衝層152與第三氮化鋁鎵緩衝層153之間、第三氮化鋁鎵緩衝層153與第四氮化鋁鎵緩衝層154之間、第四氮化鋁鎵緩衝層154與第五氮化鋁鎵緩衝層155之間插入有中間超晶格結構層130,以及一中間超晶格結構層130位於第五氮化鋁鎵緩衝層155之上。其他關於緩衝層150中的氮化鋁鎵緩衝層151-155以及中間超晶格結構層130的成分、鋁原子比例、厚度、摻質濃度以及成長方式等規則與實施例1相同。
Please refer to FIG. 9, which illustrates the type of the
在完成了前述由多個氮化鋁鎵緩衝(漸變)層151-155以及多個中間超晶格結構層130所構成的緩衝層150之後,接下來即進行後續氮化鎵磊晶層的成長。請參照第10圖,首先在緩衝層150上形成一高阻值層160,其成分可為氮化鎵,厚度介於0.5~5um之間。高阻值層160可以透過MOCVD方式在成長溫度介於1000~1200℃的環境下形成,並摻入碳、鐵、鎂以及鋅等或其組合的摻質,其摻雜物濃度介於1x1017離子/立方公分。在實施例6的例子中,最上層的中間超晶格結構層130會介於第五氮化鋁鎵緩衝層155與此高阻值層160之間。高電阻率的GaN高阻值層160可以降低GaN系的高電子遷移率電晶體(HEMTs)元件的漏電流、保持其電子氣的二維特性、提高元件的工作頻率、抑制電流崩塌效應、並提高HEMT元件的擊穿電壓。
After completing the
復參照第10圖,在形成了高阻值層160後,接下來在高阻值層160上成長一層本質氮化鎵層170,即未摻雜的氮化鎵層,其厚度介於0.2~1um之間,可以透過MOCVD方式在成長溫度介於1000~1200℃的環境下形成。本質氮化鎵層170可以做為HEMT元件的電子通道層。本質氮化鎵層170上會形成一層電子提供層(barrier layer)180,其成分可為未摻雜的氮化鋁鎵(AlhGa1-hN),其中0.1<h<0.3,厚度
介於10~40nm,成長溫度介於1000~1200度,可以透過MOCVD方式在成長溫度介於1000~1200℃的環境下形成。氮化鋁鎵的電子提供層與本質氮化鎵層170的異質接面會在該接面下形成低阻值的二維電子氣(2DEG),該二維電子氣可以使得元件具有很高的電子移動率,可做為通道來導通電流。
Referring again to Fig. 10, after the
復參照第10圖,在形成了電子提供層180之後,最後在電子提供層180上形成一覆蓋層190,其成分可以為摻雜氮化鎵或是摻雜氮化鋁鎵(AliGa1-iN),其中0.1<i<0.3。當覆蓋層190的材料為摻雜氮化鎵時,其厚度範圍約介於1~20nm,可採用碳、鐵、鎂以及鋅等或其組合的摻質。當覆蓋層190的材料為摻雜氮化鋁鎵時,其摻雜元素會選用鎂,且鎂摻雜濃度約為1x1019離子/立方公分,厚度則介於10~150nm之間。覆蓋層190可以透過MOCVD方式在成長溫度介於1000~1200℃的環境下形成。以摻雜氮化鎵或氮化鋁鎵為主的覆蓋層190有助於降低HEMT元件中的閘極漏電流並使其具有較高的崩潰電壓。在覆蓋層190形成後,後續製程中還會在覆蓋層190上製作HEMT元件的閘極、源極以及汲極等部位。由於該些部位並非本案之重點,文中與圖中將省略其說明與圖示。
Referring again to FIG. 10, after the
綜觀上述本發明實施例,本發明提出了一種改良的、具有高品質與低損耗特性的氮化鎵磊晶片,其透過將氮化鎵成長在絕緣層上覆矽晶圓上,並搭配多層漸變層以及多層中間層超晶格結構的變化來大幅緩衝氮化鎵成長時所帶來的應力,形成在絕緣層上覆矽晶圓背面的絕緣氧化層也可做為一固定層來進一步補償後續磊晶製程期間所產生的應力,避免晶圓產生習知的翹曲問題。此外,多層緩衝結構並使得整體磊晶片的厚度可超過10um,崩潰電壓可超過1000伏特,如此提升了氮化鎵元件的效率,其特別適合用來製作氮化鎵系的HEMT元件。 Looking at the above-mentioned embodiments of the present invention, the present invention proposes an improved gallium nitride epitaxial wafer with high quality and low loss characteristics, which is achieved by growing gallium nitride on a silicon-on-insulating wafer with multi-layer gradation. The changes in the superlattice structure of the layer and the multi-layer intermediate layer greatly buffer the stress brought by the growth of gallium nitride. The insulating oxide layer formed on the insulating layer on the back of the silicon wafer can also be used as a fixed layer to further compensate for the subsequent The stress generated during the epitaxy process avoids the conventional warpage problem of the wafer. In addition, the multilayer buffer structure allows the thickness of the entire epitaxial wafer to exceed 10um, and the breakdown voltage can exceed 1000 volts, which improves the efficiency of gallium nitride devices and is particularly suitable for making gallium nitride-based HEMT devices.
以上所述僅為本發明之較佳實施例,凡依本發明申請專利範圍所做之均等變化與修飾,皆應屬本發明之涵蓋範圍。 The foregoing descriptions are only preferred embodiments of the present invention, and all equivalent changes and modifications made in accordance with the scope of the patent application of the present invention shall fall within the scope of the present invention.
110:基板(絕緣層上覆矽晶圓) 110: Substrate (silicon wafer over insulating layer)
120:成核層 120: Nucleation layer
150:緩衝層 150: buffer layer
160:高阻值層 160: high resistance layer
170:本質氮化鎵層 170: Intrinsic GaN layer
180:電子提供層 180: electronic provision layer
190:覆蓋層 190: Overlay
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