TWI452722B - 二極體之結構與其製法 - Google Patents
二極體之結構與其製法 Download PDFInfo
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- TWI452722B TWI452722B TW099110301A TW99110301A TWI452722B TW I452722 B TWI452722 B TW I452722B TW 099110301 A TW099110301 A TW 099110301A TW 99110301 A TW99110301 A TW 99110301A TW I452722 B TWI452722 B TW I452722B
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- 239000000463 material Substances 0.000 title claims description 71
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 239000004065 semiconductor Substances 0.000 claims description 94
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 claims description 75
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- 238000000034 method Methods 0.000 claims description 52
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- 150000001875 compounds Chemical class 0.000 claims description 7
- 229910052594 sapphire Inorganic materials 0.000 claims description 6
- 239000010980 sapphire Substances 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 238000005229 chemical vapour deposition Methods 0.000 claims description 4
- 210000004508 polar body Anatomy 0.000 claims description 4
- NWAIGJYBQQYSPW-UHFFFAOYSA-N azanylidyneindigane Chemical compound [In]#N NWAIGJYBQQYSPW-UHFFFAOYSA-N 0.000 claims description 3
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 claims description 2
- 239000002019 doping agent Substances 0.000 claims description 2
- 238000001451 molecular beam epitaxy Methods 0.000 claims description 2
- 238000005121 nitriding Methods 0.000 claims description 2
- 210000000746 body region Anatomy 0.000 claims 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims 2
- 238000001505 atmospheric-pressure chemical vapour deposition Methods 0.000 claims 2
- 238000000231 atomic layer deposition Methods 0.000 claims 2
- 238000004518 low pressure chemical vapour deposition Methods 0.000 claims 2
- 229910052762 osmium Inorganic materials 0.000 claims 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims 2
- 229910052707 ruthenium Inorganic materials 0.000 claims 2
- 238000000038 ultrahigh vacuum chemical vapour deposition Methods 0.000 claims 2
- 238000000151 deposition Methods 0.000 claims 1
- 230000008021 deposition Effects 0.000 claims 1
- 229910002601 GaN Inorganic materials 0.000 description 36
- 239000010410 layer Substances 0.000 description 22
- 239000012535 impurity Substances 0.000 description 7
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- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 230000002269 spontaneous effect Effects 0.000 description 3
- 229910052984 zinc sulfide Inorganic materials 0.000 description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 2
- 230000001427 coherent effect Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229910052733 gallium Inorganic materials 0.000 description 2
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- 238000005304 joining Methods 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 238000001020 plasma etching Methods 0.000 description 2
- 230000005701 quantum confined stark effect Effects 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
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- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000013590 bulk material Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000002248 hydride vapour-phase epitaxy Methods 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000000608 laser ablation Methods 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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Description
本發明係有關於從結晶材料之非極性面(non-polar plane)製得之元件與其製法,例如一種III-N半導體結晶材料非極性面。於一實施例中,本發明係有關於非極性LED或其製法,且特別是有關於從III-氮化物(III-nitride)半導體結晶材料製得之非極性LED與其製法。
此部分提供背景資料,且介紹有關於下述說明書所揭露之資料,這些資料並非先前技術之證明(admission)。
氮化鎵(gallium nitride,GaN),與其與鋁和銦合併組成之三元(ternary)與四元(quanternary)化合物,已被廣泛地應用於製作可見光與紫外光光電元件與高功率(high-power)電子元件上。這些元件一般係利用磊晶成長法製得,例如分子束磊晶法(molecular beam epitaxy,MBE)、化學氣相沉積法(CVD)、金屬有機化學氣相沉積法(metalorganic chemical vapor deposition,MOCVD)與氫化物氣相磊晶法(hydride vapor phase epitaxy)。
如第1圖所示,氮化鎵與其合金最穩定之狀態是六方晶系纖鋅礦結構(hexagonal wuftzite crystal structure),此結構具有兩個(或三個)相同的基準面軸(basel plane axes),其彼此(a軸)相差120°,且垂直於一特定的c軸(c-axis)。IIIA族與氮原子交互地佔據沿著晶體c軸之c平面(c-planes)。於纖鋅礦結構中的對稱性代表III-氮化物沿著c軸擁有晶體塊材(bulk)自發性極化特性(spontaneous polarization),且纖鋅礦結構展現壓電極化特性(piezoelectric polarization)。
目前應用於電子與光電元件之氮化技術係將氮化物膜沿著極性c軸成長。然而,由於很強的壓電極化(piezodielectric)與自發性(spontaneous)極化現象,以III-氮化物(III-nitride)為主的光電與電子元件之c-平面量子井結構會產生不想要之量子侷限史塔克效應(quantum-confined Stark effect,QCSE)。沿著c軸之強烈的內建電場會使III-N材料之利用價值嚴重劣化(degrade)。
消除氮化鎵光電元件中自發性極化與壓電極化效應的方法之一,係沿著非極性面成長該材料,如晶體之m-平面(m-plane)或a-平面(a-plane)成長。這些面包含相同數量的鎵與氮原子,且為電中性。再者,後續非極性層之極性會因相等而彼此抵銷,因此晶體塊材(bulk crystal)不會沿著成長方向被極化。然而,成長具有非極性表面之氮化鎵半導體晶圓仍然存在困難。因此,需要增加III-氮化物為主之光電與電子元件(例如LEDs)之效率與提升其操作特性(operating characteristics)。
本發明的目的之一就是處理相關先前技術之問題或缺點,與提供此處敘述之優點。
為達上述與其他目的,本發明之方法主要係增加結晶材料(例如六方晶系(hexagonal)或纖鋅礦結構(wurtzite)晶體)a-平面與m-平面使用於製作電子元件之使用率。
本發明之另一方面就是要增加極性結晶材料(例如III-N材料,且特別是氮化鎵)非極性平面使用於製作電子元件之使用率。
本發明之另一方面就是要增加一半導體二極體或發光二極體(LEDs)之發光效率(extraction efficiency)或內部量子效率(internal quantum efficiency)。
本發明之另一方面就是要增加發光二極體(LEDs)之發光效率(extraction efficiency)或內部量子效率(internal quantum efficiency),藉由使用III-N半導體結晶材料之非極性面(non-polar faces)。
本發明之另一方面就是要增加發光二極體(LEDs)之發光效率(extraction efficiency)或內部量子效率(internal quantum efficiency),藉由利用III-N半導體結晶材料之非極性平面(non-polar planes)。
依照本發明之實施例,本發明提供方法,結構與裝置,其提供一半導體二極體或發光二極體(LED)包括至少一主動二極體區域,其中該主動二極體區域之非極性III-N半導體材料多於極性III-N半導體材料。
依照本發明之實施例,本發明提供方法,結構與裝置,其提供一半導體二極體或發光二極體(LED)包括由III-N半導體材料製得之底部二極體、主動二極體與頂部二極體區域,其中該主動二極體區域與頂部二極體區域每單位面積具有較底部二極體區域較少之缺陷。
依照本發明之實施例,本發明提供方法,結構與裝置,其提供一半導體二極體或發光二極體(LED)包括:一空洞(cavity)於一底部二極體材料中;一主動二極體區域於該空洞之表面上;以及一頂部二極體區域於該至少一部分的空洞中。
依照本發明之實施例,本發明提供方法,結構與裝置,其利用III-N半導體材料之非極性平面應用於LED中,以增加輸出效率。
本發明之各方面應用於具有III-N半導體之元件,包括但不限定於光電元件、發光二極體、雷射二極體與光伏打裝置。
為讓本發明之上述和其他目的、特徵、和優點能更明顯易懂,下文特舉出較佳實施例,並配合所附圖式,作詳細說明如下:
以下將詳細說明本發明概念之實施例,各種實施例伴隨著圖示顯示如下,其中類似的元件使用相同的元件符號表示。為了解釋本發明之概念,藉由參考圖示描述下述之實施例。
請參見第2圖,一二極體可包括一底部二極體區域220、一主動二極體區域230、以及一頂部二極體區域240,一第一電性接觸260位於元件之頂部,以及一第二電性接觸250位於元件之底部。每一個區域220、230、240可包括多層。二極體可以耦合至一基材210。如第2圖所示,於一實施例中,基材210可以耦合至底部電性接觸250與主動二極體區域230之間。雖然,第2圖顯示一垂直式二極體結構,然而,本發明並不限於此種結構之設置,本領域人士所熟知之其他結構與方法亦包括於本發明所保護之範圍內。
為了方便起見,此處用於標示區域所述之”頂部”與”底部”並非限定於某一區域。舉例而言,一二極體形成於一基材上,其具有頂部區域位於其底部區域之上。如果此二極體覆晶(flip-chip)接合至承載晶圓(handle wafer),且之後基材被移除,則反向(flipped)觀察二極體之符號結構。在此例中,頂部區域將會視為低於底部區域。
底部二極體區域220與頂部二極體區域240較佳具有相反(opposite)之摻雜類型。例如,底部二極體區域220主要摻雜n型(電子供給者,例如磷、砷或銻),接著,頂部二極體區域240將會摻雜p型(電子接受者,例如硼或鋁),且反之亦然。底部二極體區域220與頂部二極體區域240較佳為重摻雜(heavily doped),以改善元件的特性。
底部電性接觸250電性接觸至主動二極體區域230,例如,經由一導通孔(via)(圖中未顯示)。於另一實施例中,至少一部分之基材210之摻雜,可以與頂部二極體區域240或底部二極體區域220之主要摻雜類型(例如n型或p型)相同。因此,二極體區域與基材210之間可具有良好的電性接觸。
主動二極體區域230之示範結構端視各種因素,包括二極體及/或對應元件之特定應用。於一發光二極體(LED)中,主動二極體區域230可以是本質區域(intrinsic region)。於一發光二極體(LED)中,頂部二極體區域240、主動二極體區域230與底部二極體區域220可重複多次,以包括摻雜層與薄層未摻雜量子井(thin undoped quantum well),其中電子與電洞於薄層未摻雜量子井中再次結合且產生光子(photon)。
於另一應用於雷射之實施例中,主動區域230可以類似於發光二極體(LED)之主動區域。可加入反射層以供給產生之光源一共振腔體(resonant cavity),以製作出同調(coherent)或大體上同調的光源。
於另一應用於二極體之實施例中,主動二極體區域230只要包括介於頂部二極體區域與底部二極體區域之P-N介面(P-N junction),其可以不必是獨立成長的一層(separately grown layer)。
於另一應用於太陽能電池之實施例中,主動二極體區域230可以是適當地摻雜n-型或p-型半導體材料之單層,以吸收入射光子且產生一電子-電洞對。
III-N化合物用以形成二極體區域,已為本領域人士所熟知。III-N化合物可包括二元(binary)、三元(ternary)與四元(quanternary)形式。III-N化合物包括氮化鋁(AlN)、氮化鎵(GaN)、氮化銦(InN)與其三元與四元化合物。此處應注意的是,熟知本領域之人士應能得知如何依據所需特性(例如發光波長(emitted light wavelength)、能階(bandgap)、晶格常數(lattice constant)與摻雜程度(doping level))選擇與製作(process)這些材料。
第3圖顯示製作發光二極體(LED)之製作流程。於此例中,發光二極體(LED)由氮化鎵(GaN)結晶材料製得,但本發明不限於此種材料。例如,本發明可由其他極性材料或其他極性III-N半導體材料形成而得。於此例中,主動二極體區域形成於頂部二極體區域與底部二極體區域之間,大多數或主要之表面為非極性平面表面。於另一實施例中,介於主動區域之間的表面包括非極性m-平面(non-polar m-plane)III-N半導體面多於c-平面極性(c-plane polar)半導體面。於另一實施例中,這些表面包括非極性a-平面(non-polar m-plane)III-N半導體面多於c-平面極性(c-plane polar)半導體面。於另一實施例中,在介於主動區域之間的表面中,非極性平面之表面積為極性c-平面(polar c-plane)半導體面之表面積之至少2倍、5倍、10倍、50倍,或以上。於另一實施例中,介於主動二極體區域之頂部與底部二極體區域大體上由極性結晶材料之所有非極性表面(non-polar faces)所組成(例如,氮化鎵或其他III-N半導體材料之a-平面或m-平面之一或兩者)。於又一實施例中,主動區域之表面包括非極性III-N半導體面多於c-平面極性半導體面。
第3圖顯示一製程之實施例。如第3圖所示,於步驟310中,提供氮化鎵(GaN)層。其可以是氮化鎵塊狀基材、或氮化鎵成長(或者是形成)於一支撐物理基材上。另外,作為較大面積半導體製程之一部分時,氮化鎵(GaN)可以選擇性地成長(相對於坦覆式成長(blanket growth))於基材之特定區域中。選擇性成長可以位於一侷限的面積(confined area)中,例如於ART開口或溝槽中。於此例中,提供一習知塊狀氮化鎵(GaN)基材,其表面由極性面組成(c-平面)。於此例中,氮化鎵(GaN)之第一層對應到後續形成之LED的底部二極體區域220。當進行一般成長製程時,由於III-N半導體材料特性的關係,傳統的塊狀極性基材具有平行於基材的c-平面。
於步驟320中,使氮化鎵(GaN)暴露出a-平面或m-平面之一或兩者。舉例而言,垂直蝕刻氮化鎵(GaN)以形成開口,例如,於氮化鎵(GaN)表面中形成孔洞(hole)或溝槽(trench)。此種設計之氮化鎵(GaN)即作為元件底部二極體區域。
於步驟330中,形成主動二極體區域。依據所設計出的元件,此步驟可與步驟340(如下所述)分離或成為步驟340的一部分。例如,如果一發光二極體(LED)具有本質區域(intrinsic region),步驟330可包括磊晶成長未摻雜氮化鎵於步驟320形成之氮化鎵表面上。於另一實施例中,如果形成二極體,步驟330可以是步驟340之初始步驟,以形成PN介面(例如,包括空乏區域(depletion region))。
於步驟340中,形成一頂部二極體區域。舉例而言,此步驟可包括磊晶成長氮化鎵(GaN)於步驟330之結構上,此氮化鎵之摻雜類型與步驟310之氮化鎵的摻雜類型不同。例如,如果步驟310之氮化鎵摻雜n型雜質,則步驟340之氮化鎵摻雜p型雜質。如果步驟310之氮化鎵摻雜p型雜質,則步驟340之氮化鎵摻雜n型雜質。
於步驟350中,可加上電性接觸(contact),以提供電性連接至頂部與底部二極體區域。雖然第3圖顯示步驟310~步驟350進行之程序(order),然而,本發明不應該被侷限於此進行之程序。於另一實施例中,可於製程中的任何時機點形成電性接觸(例如,可先形成於各自的基材上,之後再將二極體區域連接)。
第4圖顯示一習知極性氮化鎵層塊材(GaN layer)。如第4圖所示,極性氮化鎵層形成於藍寶石(sapphire)晶圓基材上,也可使用其他基材,例如矽或碳化矽(silicon carbide)。基材100例如可以是塊狀矽晶圓、塊狀鍺晶圓、絕緣層上覆半導體(semiconductor-on-insulator,SOI)基材、或應力絕緣層上覆半導體(strained semiconductor-on-insulator,SSOI)基材。基材100可包括第一半導體材料或主要由一第一半導體材料所組成,例如藍寶石。藍寶石晶圓基材之晶向一般為(1,0,0),然而,本發明之實施例並不限於此晶向。
成長氮化鎵於藍寶石上已為本領域人士所熟知,然而,結晶材料的缺陷(defect)程度卻很高(例如109
/cm2
),其缺陷主要來自錯位缺陷(dislocation defect)。然而,如第4圖所示,大多數的錯位缺陷發生於垂直或大體上垂直於III-N材料的c-平面。因此,於一實施例中,於氮化鎵塊材之垂直側壁將會具有較少數目的缺陷(例如,垂直側壁之每單位表面面積會比水平平面具有較少的缺陷)。
提供氮化鎵塊材之後,移除某些特定部分(selected portions),以留下某些不朝向c-平面的結構。例如,移除特定部分,以留下從基材頂部表面延伸之平面,該平面之投影(projections)方向不朝向c-平面。於一實施例中,為了使用氮化鎵材料之m-平面或a-平面,因此設置投影部分(如步驟320)。於一實施例中,所設置的投影部分不使用氮化鎵材料之c-平面。可蝕刻氮化鎵塊材以具有指定尺寸之開口(openings),例如孔洞(holes)、凹口(recesses)或空隙(cavity)。這些溝槽(trenches)可用習知的微影技術(photolithogrphy)或反應性離子蝕刻製程(reactive ion etching,RIE)製得。如第5圖所示,結晶材料的剩餘結構520或投影(projections)可包括第一部分524(例如,平面側),其沿著非極性平面(例如,m-平面或a-平面)延伸,而特定部份522朝向c-平面。於一實施例中,側壁524之尺寸為特定部份522的2倍、5倍、10倍、20倍或100倍。於一實施例中,此設計可被設置作為鰭(fins)或柱(posts)。於一實施例中,一底部表面可具有一特定設計(例如,一特定斜率或指定的輪廓,如V型)。
如上所述,底部二極體區域220可以於磊晶成長期間原處(in situ)摻雜或非原處(ex situ)離子佈植。再者,底部二極體區域的材料較佳視元件的需求而定。
於一實施例中,可形成氮化鎵塊材內的溝槽530,其具有大體上m-平面或a-平面側壁(例如,依據結構的排列方向(orientation)不同,可以是垂直或水平側壁)。溝槽的數目視所需要的應用可以是1個或甚至是數百個。
當底部二極體區域被設置之後,形成一主動二極體區域(如步驟330)。於一實施例中,主動二極體區域可以是磊晶成長。如第6圖所示,磊晶成長的示範方向如箭頭610所示。主動二極體區域230於曝露的氮化鎵表面的投影(projections)之頂部、底部或水平面(horizontal planes)522之成長是垂直地成長。主動二極體區域230位於曝露的氮化鎵表面的投影(projections)之側壁(sides)或垂直平面(vertical planes)524之成長可以是水平地成長。示範的主動二極體區域230可以於磊晶成長期間原處(in situ)摻雜或非原處(ex situ)離子佈植。於一實施例中,主動二極體區域230可以是本質的(例如,本質摻雜(intrinsically doped))
一般而言,存在於磊晶成長表面上的缺陷將導致材料連續地長出缺陷,形成具缺陷的成長表面(defective growth surface)。於主動二極體區域磊晶成長期間,缺陷的擴張(extension of defect)並未顯示於第6圖中。然而,既然於氮化鎵中的缺陷主要是垂直的(請參見第4圖與第5圖),因此缺陷多數平行於曝露的投影之側壁。許多或大多數的缺陷並不會與投影的側壁交叉(intersect),且這些側壁將具有減少的或大體上無缺陷的表面。因此,於第6圖中成長於投影之側壁上的主動二極體區域之缺陷度(defectvity)將會降低或大體上不存在。成長於這些側壁上的主動區域的缺陷密度(defect density)會低於底部二極體區域220之缺陷密度。如第6圖所示,於主動二極體區域230中的虛線部份630a將具有低於底部二極體區域220之缺陷密度。於一實施例中,於主動二極體區域230中的缺陷度較底部二極體區域220低2倍、5倍、10倍、20倍或更多。
形成主動二極體區域230之後,再形成頂部二極體區域(步驟340)。於一實施例中,磊晶成長一示範的頂部二極體區域240。如第7圖所示,頂部二極體區域240之磊晶成長類似於主動二極體區域之磊晶成長(例如,磊晶成長的方向類似於第6圖之箭頭610)。頂部二極體區域240於曝露的氮化鎵表面的投影(projections)(例如,主動二極體區域)之頂部、底部或水平面(horizontal planes)522之成長是垂直地成長。頂部二極體區域240於曝露的氮化鎵表面的投影(projections)之側壁(sides)或垂直平面(vertical planes)524之成長是水平地成長。第7圖之特徵之一是,頂部二極體區域240可以部分(圖中並未顯示)或完全填充於一開口中,例如開口530或位於主動二極體區域230中的開口。第7圖之特徵之一是,頂部二極體區域240可以填充多層開口/溝槽,使得在多層開口/溝槽中形成頂部二極體區域240與主動二極體區域230的電性接觸。此結構特別有助於發光二極體(LED),因為其可以降低或減少底部電性接觸260的面積,以避免底部電性接觸260阻擋從主動二極體區域230中發射出的光。示範的頂部二極體區域240可以於磊晶成長期間原處(in situ)摻雜或非原處(ex situ)離子佈植。較佳地,發光二極體(LED)之頂部二極體區域240重摻雜一與底部二極體區域220相反類型的雜質。
於一實施例中,於頂部二極體區域中的缺陷程度(defect levels)少於底部二極體區域。於另一實施例中,頂部二極體區域之缺陷程度多於主動二極體區域。依據一實施例,頂部二極體區域240之缺陷度(defectivity)可以比底部二極體區域220低2倍、5倍、10倍、20倍或更多。
於一實施例中,至少主動二極體區域之成長條件可以設定或設計成傾向從m/a平面(例如,524表面)水平成長多於傾向從c-平面(例如,522表面)成長。
當頂部二極體區域完成後,可視需要的(optionally)選擇如本領域人士所熟知之額外製程步驟,以完成對應的半導體零件、半導體元件、或半導體產品(步驟350)。舉例而言,一些實施例中,可加入頂部與底部電性接觸(步驟350)。此外,示範之實施例包括接合到導電晶圓上、接合到一晶粒(die)或接合到封裝固定點(package mounting point)、移除基材與加上頂部與底部電性接觸,或類似之步驟。
當頂部二極體區域240形成之後,可形成如第8圖所示之電性接觸(步驟350)。於一實施例中,對於每一個開口/溝槽提供一頂部電性接觸814與底部電性接觸812,以分別直接接觸頂部二極體區域220與底部二極體區域240。可藉由本領域人士所熟知之各種材料/製程形成電性接觸812、814。適合用於形成電性接觸之材料,例如,可包括條狀(strip)導電金屬(如銅、銀或鋁)、反射導電材料或一層相對透明的導電材料(例如氧化銦錫)。再者,有許多方法可穿過基材電性接觸底部電性接觸812與底部二極體區域220,以達到一電性接觸,例如接觸導通孔(contact via)。電性接觸812、814可各自操作作為頂部電性接觸260與底部電性接觸250。於另一實施例中,可對於複數個頂部二極體區域240或複數個底部二極體區域220(例如,於複數個開口/溝槽中)提供單一的電性接觸(例如,812與814)。
對於特定發光二極體(LED)的應用,基材210可能降低元件的性能(例如,吸收光)。於一示範的實施例中,如第9圖所示,可移除基材210,藉由此領域已知的方法,例如磨削(grinding)、蝕刻(etching)、雷射剝離(laser ablation)或類似的方法。一示範製程(步驟350)可包括接合一”承載(handle)”基材或單元910到頂部二極體區域240,且加入電性接觸912、914。於接合承載基材910至頂部二極體區域240之前,頂部二極體區域240之對應表面藉由一合適的方法(例如化學機械研磨法(CMP))平坦化,以確保承載基材910之附著(attach)。此外,可使用一連接劑或層(圖中並未顯示)以確保承載基材910電性連接至頂部二極體區域240。再者,可使用一黏著劑或膠層(圖中未顯示)以確保承載基材910接合至頂部二極體區域240。
之後,藉由標準技術加入頂部電性接觸260與底部電性接觸250。如第9圖所示,對於2個或多個開口/溝槽或於主動區域230中的對應開口/溝槽,可提供一個頂部電性接觸914與一個底部電性接觸912。另外地,此承載基材910可以是電性導電的。於一實施例中,對於頂部二極體區域240,承載基材910可包括或整合頂部電性接觸914。再者,承載基材910可包括或電性耦合至一元件或封裝體。
於發光二極體(LED)相關領域中,限制內部量子效率(internal quantum efficiency)的一個因素在於,氮化鎵之極性c-平面面對主動區域。如第3圖顯示之示範實施例及/或第8-9圖顯示之示範實施例可以傳輸較高的內部量子效率,因為氮化鎵(GaN)的非極性m-平面或a-平面面對主動二極體區域。再者,對於一或多個底部二極體區域220、主動二極體區域230及/或頂部二極體區域240而言,此類實施例可以提供發光二極體(LED)結構具有較少的c-平面方向的氮化鎵(GaN)材料。
於一實施例中,氮化鎵(GaN)之非極性m-平面或a-平面可以形成一介面(interface)介於底部二極體區域220與主動二極體區域230之間。於一實施例中,氮化鎵(GaN)之非極性m-平面或a-平面可以形成一介面(interface)介於主動二極體區域230與頂部二極體區域240之間。
依據所應用之特定實施例,於一對應元件中,需要增加非極性平面氮化鎵(GaN)對於極性平面氮化鎵(GaN)之比例。於一示範實施例中,可以增加非極性平面氮化鎵(GaN)相對於極性氮化鎵(GaN)之部分,藉由相對增加側壁524之尺寸或降低底部表面522之尺寸。於一示範之實施例中,可以增加非極性平面氮化鎵(GaN)相對於極性氮化鎵(GaN)之部分,藉由於製程中移除極性氮化鎵(GaN)之特定部份。第10a-10b圖顯示一半導體二極體之示範結構。如第10a圖所示,可以減少或移除頂部二極體區域1040中含有極性c-平面氮化鎵的部分。如第10a圖中,底部表面之移除停止於頂部二極體區域,然而,此實施例並非用以限定本發明。例如,可連續移除氮化鎵(GaN)材料,直到進入主動二極體區域。如第10b圖所示,於頂部二極體區域1040中含有極性c-平面氮化鎵的部分可被移除或被頂部電性接觸1014a取代。參考符號1016可以指平坦層,例如絕緣層(insulator)。
於一示範實施例中,相對於極性平面氮化鎵(GaN),可以增加非極性平面氮化鎵(GaN)的部分,藉由於製程期間,減少或移除極性平面氮化鎵(GaN)材料之特定部份。第10c圖顯示一半導體二極體之示範結構,其中於形成頂部二極體區域1040之前,移除含有主動二極體區域1030之極性平面氮化鎵(GaN)的部分。第10d圖顯示一半導體二極體之示範結構,其中於形成一”承載(handle)”基板910’之前,移除底部二極體區域1020、主動二極體區域1030及/或頂部二極體區域之極性平面氮化鎵(GaN)。於一實施例中,從空乏區(depletion region)、主動二極體區域或半導體二極體中,可以刪除(例如,移除)大體上成長於且排列於c-平面之所有極性平面氮化鎵(GaN)材料。
再者,於特定實施例中,頂部電性接觸及/或底部電性接觸可以是2維或3維結構,以減少光撞擊到位於至少一底部二極體區域、主動二極體區域或頂部二極體區域之極性氮化鎵(GaN)材料。
於應用於發光二極體(LED)之一實施例中,頂部電性接觸(例如,220)可以是高度反射導電材料,其可以反射內部產生的光,使其從一特定表面或所需表面中離開發光二極體(LED)。例如,反射底部電性接觸可以由材料(例如銀)製得。於另一實施例中,可以使用此種反射底部電極並連接光穿透基材或光學半透明/透明(translucent/transparent)基材。
應用於發光二極體(LED)之一實施例中,反射層可合併於相鄰之底部二極體區域220、主動二極體區域230及/或頂部二極體區域240之一,以直接反射內部產生的光,使其從一特定表面或所需表面中離開發光二極體(LED)。例如,反射層可以直接介於頂部二極體區域220與基材210之間。反射層可由本領域人士所熟知之材料/製程製得。
應用於半導體二極體之一實施例中,其可包括一具有第一雜質(dopant)類型之第一區域、一主動區域與一具有相反於第一雜質之第二雜質類型之第二區域,其中主動區域介於第一區域與第二區域之間。主動區域位於第一或第二區域之非極性平面表面中,或介於第一與第二區域中的至少一非極性平面表面之間。因此,半導體二極體具有一水平或垂直堆疊結構。相鄰於主動區域之第一區域的非極性表面/極性表面之比率大於1。於一實施例中,至少一主動區域是III-N半導體材料。於另一實施例中,主動區域是pn介面或pn介面之空乏區(depletion region)。於又一實施例中,主動區域是介於第一區域與第二區域之間的本質(intrinsic)區域或量子井(quantum well)結構。於此說明書中,空乏區(depletion region)可以是主動二極體或主動區域其中之一的類型。形成第一電性接觸與第二電性接觸對應到第一與第二區域。
發射光的波長以及其顏色,端視所形成之發光二極體(LED)p-n介面的材料能階能量(band gap energy)。發光二極體(LEDs)合併III-N半導體材料可以發射光,包括藍光、綠光、紅外光、紫外光與白光(例如,以藍光為基礎或合併藍光)。舉例而言,藍光發光二極體(LEDs)係依據寬能階之氮化鎵(GaN)與氮化銦鎵(InGaN)半導體。於傳統的發光二極體(LEDs),限制內部量子效率(internal quantum efficiency)之因素在於,氮化鎵(GaN)的極性c-平面。可藉由發光之顏色/波長而改變主動區域或對應發光二極體(LED)元件之內部效率之降低程度。於一實施例中,預期綠光發光二極體(LED)之效率可以增加超過100倍。於另一實施例中,預期綠光發光二極體(LED)之效率可以增加超過2倍、5倍、10倍或更多。
依據應用之藍光發光二極體(LED)或白光發光二極體(LED)之一實施例中,因為非極性III-N半導體結晶材料,可以使其效率增加大於2倍、大於5倍、大於10倍、大於25倍或更多。
依據應用之紅外光(infrared light)發光二極體(LED)之一實施例中,因為非極性III-N半導體結晶材料,可以使其效率增加大於2倍、大於5倍、大於10倍、大於25倍或更多。
依據應用紫外光(ultraviolet light)發光二極體(LED)之一實施例中,因為非極性III-N半導體結晶材料,可以使其效率增加大於2倍、大於5倍、大於10倍、大於25倍或更多。
於一示範實施例中,頂部與底部二極體區域之摻雜程度可以介於1017
-1020
cm-3
,而主動區域之摻雜程度可以低於1017
cm-3
。
由於使用極性材料,使得雷射發光二極體(lasers LEDs)具有下述缺點,包括至少一不想要的頻率偏移(frequency shift)及/或效率之損失。依據本發明之應用,可以降低上述缺點。
雖然示範的實施例使用氮化鎵(GaN),然而,可以了解的是,亦可使用其他III-N半導體材料。依據本發明之實施例,可以提供一III-N半導體材料(例如,選擇性磊晶成長)。於一些實施例中,可以提高沿著III-N結晶半導體材料之第一方向的成長,可以減少沿著III-N結晶半導體材料之第二方向的成長。於一些實施例中,非極性平面III-N半導體材料之成長可多於極性平面III-N半導體材料之成長。於一些實施例中,可以提高a-平面/m-平面方向的III-N結晶半導體材料之成長,及/或可以減少c-平面方向III-N結晶半導體材料之成長。
雖然此處敘述之實施例係使用非極性平面,應能了解的是,也可使用可以降低或消除c-平面III-N半導體材料之特徵缺點的任何方向(例如,半平面(semi-planar)或半極性(semi-polar))。
示範的半導體二極體可用於單一二極體或主動二極體區域中,然而,熟知本領域之人士應能了解的是,大多數的應用需要多重二極體,一般整合於單一晶片(chip)上。如果複數個此種半導體零件、元件或產品形成用於單一元件或單一晶片上,其較佳具有相同的電性結構與大體上相同的效能。
如上所述,本發明具有廣泛的應用。不限於發光二極體技術,本發明具有許多在發光二極體(LED)技術領域中的應用。
說明書中出現之用語”於一個實施例”或”於一實施例”意指一特定之結構特徵(feature)、結構(structure)或特性(characteristic)包含於至少本發明之一實施例中。因此,出現於說明書中各處之用語”於一個實施例”或”於一實施例”並不代表相同的實施例。再者,當一特定結構特徵(feature)、結構(structure)或特性(characteristic)描述於任一實施例中,熟知本領域之人士可影響此種結構特徵、結構或特性與其他實施例之連接關係。此外,為了簡化說明,某些方法步驟可以描述成獨立的製程;這些獨立的製程可以不必依特定的順序(necessarily order)呈現。另言之,一些製程步驟可以以交替的順序(alternative ordering)或同時的(simultaneously)方式進行。此外,示範的圖形用於敘述本發明之各種實施例。此處敘述之各種示範實施例,其可以對應到裝置的實施例,然而,方法的實施例並非限定於此。
雖然本發明已以數個較佳實施例揭露如上,然其並非用以限定本發明,任何所屬技術領域中具有通常知識者,在不脫離本發明之精神和範圍內,當可作任意之更動與潤飾,因此本發明之保護範圍當視後附之申請專利範圍所界定者為準。
100...基材
210...基材
220...底部二極體區域
230...主動二極體區域
240...頂部二極體區域
250...底部電性接觸
260‧‧‧頂部電性接觸
310‧‧‧提供氮化鎵(GaN)層
320‧‧‧設置具有a-平面或m-平面之氮化鎵(GaN)
330‧‧‧形成一主動二極體區域
340‧‧‧形成一頂部二極體區域
350‧‧‧視需要的加上頂部電性接觸、底部電性接觸及/
或承載基材(handle substrate),以完成元件
520‧‧‧剩餘結構
522‧‧‧特定部份
524‧‧‧第一部分
530‧‧‧溝槽
610‧‧‧箭頭
630a‧‧‧虛線部份
812‧‧‧底部電性接觸
814‧‧‧底部電性接觸
910、910’‧‧‧承載載材(handle substrate)
912‧‧‧底部電性接觸
914‧‧‧頂部電性接觸
1014、1014a‧‧‧頂部電性接觸
1016‧‧‧平坦層
1020‧‧‧底部二極體區域
1030‧‧‧主動二極體區域
1040‧‧‧頂部二極體區域
第1a-1c圖為一透視圖,用以說明包括c-平面、m-平面與a-平面之六方晶系結晶結構。
第2圖為一剖面圖,用以說明本發明半導體二極體之設置。
第3圖為一流程圖,用以說明本發明形成一半導體二極體之方法。
第4圖為一剖面圖,用以說明氮化鎵層位於基材上的結構。
第5-7圖為一剖面圖,用以說明包括非極性面之III-N主動區域之發光二極體結構。
第8圖為一剖面圖,用以說明包括朝向非極性平面的III-N主動區域之半導體二極體結構的實施例,其係應用於示範之LED元件。
第9圖為一剖面圖,用以說明包括朝向非極性平面的III-N主動區域之半導體二極體結構的實施例,其係應用於示範之LED元件。
第10a-10d圖為一剖面圖,用以說明包括非極性III-N主動區域之半導體二極體結構的實施例,其係應用於示範之LED元件。
310...提供氮化鎵(GaN)層
320...設置具有a-平面或m-平面之氮化鎵(GaN)
330...形成一主動二極體區域
340...形成一頂部二極體區域
350...視需要的加上頂部電性接觸、底部電性接觸及/或承載基材(handle substrate),以完成元件
Claims (55)
- 一種二極體(diode)之製作方法,包括以下步驟:形成一第一二極體區域於一基材之上,該一第一二極體區域包括具有一或多個孔洞形成於其中之一第一表面,其中該一或多個孔洞之側壁係為一極性半導體結晶材料之非極性表面;形成一第二二極體區域相對於該第一表面;以及形成一主動區域,設置於該第一二極體區域與該第二二極體區域之間,且至少部分延伸至一或多個孔洞中。
- 如申請專利範圍第1項所述之二極體之製作方法,其中相鄰於該主動區域之第一二極體區域之一或多個表面之一面積為非極性,且該第一二極體區域之一或多個表面之一面積為極性,且其中該非極性之面積大於該極性面積。
- 如申請專利範圍第1項所述之二極體之製作方法,其中至少一部分之該主動區域與該第二二極體區域對應到III-N半導體結晶材料之非極性平面(non-polar plane)。
- 如申請專利範圍第1項所述之二極體之製作方法,其中:該第一二極體區域包括一底部二極體區域,其中該底部二極體區域是由一III-N半導體材料所形成;該主動區域包括一主動二極體區域相鄰於該底部二極體區,其中該主動二極體區域是由一III-N半導體材料所形成;以及該第二二極體區域包括一頂部二極體區域相鄰於該主動二極體區域,其中該頂部二極體區域是由一III-N半導體材料所形成,其中該主動二極體區域與該頂部二極體區域之每單位面積相較於該底部二極體區域具有較少之缺陷(defect)。
- 如申請專利範圍第1項所述之二極體之製作方法,其中:該第一二極體區域,該主動區域,以及該第二二極體區域是由III-N半導體材料所形成;以及提供一非極性(non-polar)III-N半導體材料於該發光二極體中,以增加一輸出效率(output efficiency)至超過一規定量(prescribed amount)。
- 如申請專利範圍第1項所述之二極體之製作方法,其中:該第一二極體區域包括一III-N半導體結晶層於一極性平面(polar plane)上;該第一二極體區域包括一底部二極體區域,其中該底部二極體區域包括至少一第一表面與至少一第二表面,且其中該第一表面對準於該III-N半導體材料之一非極性表面,該第二表面對準於該III-N半導體材料之一極性表面;該主動區域相鄰於該底部二極體區域之至少該第一表面與至少該第二表面;以及該第二二極體區域包括一頂部二極體區域,其中該頂部二極體區域相鄰於該主動二極體區域。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該主動二極體區域具有一第一部分與一第二部分,該第一部分具有一第一光輸出效率(first output light efficiency),該第二部分具有一較低之第二光輸出效率。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該主動區域與該第一二極體區域至少之一具有比該第二二極體區域較多的線缺陷總數(total line defects)。
- 如申請專利範圍第1項所述之二極體之製作方法,其中於藍光LED、綠光LED、白光LED、紫外光(ultraviolet light)LED或紅外光(infrared light)LED中,該光輸出效率大於約2倍,大於約5倍,大於約10倍或大於約25倍。
- 如申請專利範圍第4項所述之二極體之製作方法,其中於面對主動區域之底部二極體區域中,非極性平面之表面積比極性平面之表面積大於2,大於4,大於10或大於50。
- 如申請專利範圍第4項所述之二極體之製作方法,其中至少一朝向III-N半導體材料之極性表面之一部分主動二極體區域、朝向III-N半導體材料之極性表面之一部分頂部二極體區域、朝向III-N半導體材料之極性表面之一部分底部二極體區域少於50%,少於25%,少於15%,少於10%,或少於5%。
- 如申請專利範圍第4項所述之二極體之製作方法,其中朝向III-N半導體材料之非極性表面(non-polar surface)之一部分主動二極體區域、底部二極體區域或頂部二極體區域大於50%,大於75%,大於85%,或大於95%。
- 如申請專利範圍第1項所述之二極體之製作方法,其中至少一該第一二極體區域,該主動區域,以及該第二二極體區域包括下述一或多個:氮化鋁(AlN)、氮化鎵(GaN)、氮化銦(InN)、或上述之三元(ternary)或四元(quaternary)化合物。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該一或多個孔洞包括溝槽(trench)、凹口(recess)或孔洞(hole)。
- 如申請專利範圍第1項所述之二極體之製作方法,尚包括:一半導體元件形成於該一或多個孔洞。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該一或多個孔洞之深度(width)大於寬度2倍,至少5倍,至少10倍,或至少100倍。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該一或多個孔洞之長度大於寬度至少10倍,或至少100倍。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該基材包括矽、鍺或藍寶石(sapphire)。
- 如申請專利範圍第1項所述之二極體之製作方法,其中曝露於該一或多個孔洞中之該基材之一表面係為該矽基材之(100)表面,且其中該基材是單晶或多晶基材。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該第一二極體區域,該主動區域,以及該第二二極體區域為相同的半導體結晶材料。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該第一二極體區域之半導體結晶材料至少與該主動區域或該第二二極體區域不同。
- 如申請專利範圍第1項所述之二極體之製作方法,其中至少二該第一二極體區域、該主動區域與該第二二極體區域摻雜不同摻雜濃度。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該主動區域與該第二二極體區域至少之一由選擇性磊晶成長法(selective epitaxial growth)製得,其中該選擇性磊晶成長法包括:金屬有機化學氣相沉積法(metal-organic chemical vapor deposition,MOCVD)、常壓化學氣相沉積法(atmosphere-pressure CVD,APCVD)、低壓化學氣相沉積法(low-(or reduced-)pressure CVD,LPCVD)、超高真空化學氣相沉積法(ultra-high-vacuum CVD,UHCVD)、分子束磊晶法(molecular beam epitaxy,MBE)或原子層沉積法(atomic layer deposition,ALD)。
- 如申請專利範圍第1項所述之二極體之製作方法,其中至少二該第一二極體區域,該主動區域,與該第二二極體區域為重複排列(repeated)。
- 如申請專利範圍第1項所述之二極體之製作方法,其中至少一對應到一極性面之至少一部分該第一二極體區域、該主動區域與該第二二極體區域被移除。
- 如申請專利範圍第1項所述之二極體之製作方法,其中該主動區域包括一本質(intrinsic)主動區域或一空乏區(depletion region)。
- 一種二極體(diode),包括:一第一二極體區域於一基材之上,該一第一二極體區域包括具有一或多個孔洞形成於其中之一第一表面,其中該一或多個孔洞之側壁係為一極性半導體結晶材料之非極性表面;一第二二極體區域相對於該第一表面;以及一主動區域,設置於該第一二極體區域與該第二二極體區域之間,且至少部分延伸至一或多個孔洞中。
- 如申請專利範圍第27項所述之二極體,其中:相鄰於該主動區域之第一二極體區域之一或多個表面之一面積為非極性,且該第一二極體區域之一或多個表面之一面積為極性,且其中該非極性之面積大於該極性面積。
- 如申請專利範圍第27項所述之二極體,其中:該主動區域之至少一部分對應到該第一二極體區域之非極性平面(non-polar plane)。
- 如申請專利範圍第27項所述之二極體,其中:該第一二極體區域包括一底部二極體區域,由一III-N半導體材料形成而得;該主動區域包括一主動二極體區域,從一III-N半導體材料形成而得且相鄰於該底部二極體區域;以及該第二二極體區域包括一頂部二極體區域,從一 III-N半導體材料形成而得且相鄰於該主動二極體區域,其中該主動二極體區域與該頂部二極體區域比該底部二極體區域每單位面積具有較少之缺陷(defect)。
- 如申請專利範圍第30項所述之二極體,其中:該底部二極體區域、該主動二極體區域與該頂部二極體區域是由III-N半導體材料形成而得,其中於該LED中形成非極性III-N半導體材料以增加一輸出效率。
- 如申請專利範圍第27項所述之二極體,其中:該第一二極體區域包括一III-N半導體結晶層之一底部二極體區域,該底部二極體區域位於一極性面,其中該底部二極體區域具有至少一第一表面與一第二表面,其中該第一表面對準於III-N半導體結晶層之一非極性面,該第二表面對準於III-N半導體結晶層之極性面;該主動區域包括一主動二極體區域,相鄰於該底部二極體區域之至少一第一表面與第二表面;以及該第二二極體區域包括一頂部二極體區域,相鄰於該主動二極體區域。
- 如申請專利範圍第27項所述之二極體,其中:該第一二極體區域包括一III-N半導體材料之一底部二極體區域;該主動區域包括一主動二極體區域,相鄰於該底部二極體區域,且位於III-N半導體材料之非極性表面(non-polar surface)上;以及該第二二極體區域包括一頂部二極體區域,相鄰於該主動二極體區域。
- 如申請專利範圍第27項所述之二極體,其中:該主動區域具有一第一部分與一第二部分,該第一部分具有一第一光輸出效率,該第二部分具有低於該第一光輸出效率之第二光輸出效率。
- 如申請專利範圍第27項所述之二極體,其中該主動區域是III-N半導體材料,其對應到一非極性表面。
- 如申請專利範圍第30項所述之二極體,其中該主動區域與該頂部區域至少之一具有比該底部二極體區域較多的線缺陷總數(total line defects)。
- 如申請專利範圍第27項所述之二極體,其中於藍光LED、綠光LED、白光LED、紫外光(ultraviolet light)LED,或紅外光(infrared light)LED中,該光輸出效率大於約2倍,大於約5倍,大於約10倍或大於約25倍。
- 如申請專利範圍第30項所述之二極體,其中於面對主動區域之底部二極體區域中,非極性平面之表面積比極性平面之表面積大於2,大於4,大於10或大於50。
- 如申請專利範圍第31項所述之二極體,其中至少一朝向III-N半導體材料之極性表面之一部分主動二極體,朝向III-N半導體材料之極性表面之一部分頂部二極體區域,朝向III-N半導體材料之極性表面之一部分底部二極體區域少於50%,少於25%,少於15%,少於10%,或少於5%。
- 如申請專利範圍第31項所述之二極體,其中朝向III-N半導體材料之非極性表面之一部分主動二極體區域、底部二極體區域或頂部二極體區域大於50%,大於75%,大於85%,或大於95%。
- 如申請專利範圍第27項所述之二極體,其中至少一該第一二極體區域,該主動區域,以及該第二二極體區域包括下述一或多個:氮化鋁(AlN)、氮化鎵(GaN)、氮化銦(InN)、或上述之三元(ternary)或四元(quaternary)化合物。
- 如申請專利範圍第27項所述之二極體,其中該一或多個孔洞包括溝槽(trench)、凹口(recess)或孔洞(hole)。
- 如申請專利範圍第27項所述之二極體,尚包括:一半導體元件形成於該一或多個孔洞。
- 如申請專利範圍第27項所述之二極體,其中該一或多個孔洞之深度大於寬度(width)至少2倍,至少5倍,至少10倍,或至少100倍。
- 如申請專利範圍第27項所述之二極體,其中該一或多個孔洞之長度大於寬度至少10倍,或至少100倍。
- 如申請專利範圍第27項所述之二極體,其中該基材包括矽、鍺或藍寶石(sapphire)。
- 如申請專利範圍第27項所述之二極體,其中曝露於該一或多個孔洞中之該基材之一表面係為該矽基材之(100)表面,且其中該基材是單晶或多晶基材。
- 如申請專利範圍第27項所述之二極體,其中該第一二極體區域,該主動區域,以及該第二二極體區域為相同的半導體結晶材料。
- 如申請專利範圍第27項所述之二極體,其中至少二該第一二極體區域,該主動區域,以及該第二二極體區域之半導體結晶材料如申請專利範圍第27項所述之二極體不同。
- 如申請專利範圍第27項所述之二極體,其中至少二該第一二極體區域,該主動區域,以及該第二二極體區域摻雜不同摻雜濃度。
- 如申請專利範圍第27項所述之二極體,其中該第一二極體區域與該第二二極體區域摻雜不同類型之雜質(dopants)。
- 如申請專利範圍第27項所述之二極體,其中該第一二極體區域,該主動區域,以及該第二二極體區域為重複排列(repeated)。
- 如申請專利範圍第27項所述之二極體,該第一二極體區域,其中對應到一極性面之至少一部分該主動區域被移除。
- 如申請專利範圍第27項所述之二極體,該第一二極體區域,其中對應到一極性面之至少一部分該第一二極體區域或第二二極體區域被移除。
- 如申請專利範圍第27項所述之二極體,其中該主動區域包括一本質(intrinsic)主動區域或一空乏區(depletion region)。
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US20160211260A1 (en) | 2016-07-21 |
KR101450956B1 (ko) | 2014-10-15 |
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