TWI692886B - 具有改善光提取之電致發光二極體的光電裝置 - Google Patents
具有改善光提取之電致發光二極體的光電裝置 Download PDFInfo
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- TWI692886B TWI692886B TW108102133A TW108102133A TWI692886B TW I692886 B TWI692886 B TW I692886B TW 108102133 A TW108102133 A TW 108102133A TW 108102133 A TW108102133 A TW 108102133A TW I692886 B TWI692886 B TW I692886B
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Abstract
本發明關於一種光電裝置(5),光電裝置(5)包括半導體基板(10)、發光二極體(DEL)及至少部分透明的介電層(34),半導體基板(10)包括表面(12),發光二極體(DEL)由該表面所支撐且包括線型、圓錐形或錐形的半導體元件(20),至少部分透明的介電層(34)覆蓋發光二極體,介電層之折射率在從1.6至1.8的範圍中。
Description
本發明大致上關於基於半導體材料的光電裝置及製造該等光電裝置的方法。本發明更具體而言關於包括由三維元件所形成的發光二極體的光電裝置,三維元件特定而言為半導體微米線或奈米線。
用語「具有發光二極體的光電裝置」指明能夠將電子訊號轉換成電磁輻射的裝置,且更特定而言專用於電磁輻射(特定而言為光)之發射的裝置。能夠形成發光二極體的三維元件之實例為包括半導體材料的微米線或奈米線,該半導體材料是基於主要包括至少一個第三族元素及一個第五族元素的化合物(舉例而言,氮化鎵(GaN)),以下稱作III-V族化合物。
光電裝置之提取效率通常由從光電裝置逃脫的光子之數目對於由發光二極體所發射的光子之數目之比例所界定。希望光電裝置之提取效率盡可能高。
現存光電裝置之缺點為在各發光二極體內發射的一小部分光子並不從發光二極體逃脫。
現存光電裝置之另一個缺點為由各發光二極體所發射的光之一部分被鄰近發光二極體所捕捉或吸收。
因此,實施例之目的為克服先前所述具有發光二極體且特定而言具有微米線或奈米線的光電裝置及該等光電裝置之製造方法之至少部分的缺點。
實施例之另一個目的為增加光電裝置之提取效率。
實施例之另一個目的為減少並不從各發光二極體逃脫的光之比例。
實施例之另一個目的為減少由發光二極體所發射的光被鄰近發光二極體所吸收/捕捉之比例。
實施例之另一個目的為針對具有發光二極體的光電裝置能夠以產業規模且於低成本下製造。
因此,實施例提供光電裝置,包括: 半導體基板,該半導體基板包括表面; 由該表面所支撐的發光二極體,且包括線型、圓錐形(conical)或錐形(tapered)的半導體元件;及 至少部分透明的介電層,該至少部分透明的介電層覆蓋該等發光二極體,介電層之折射率在從1.6至1.8的範圍中。
根據實施例,介電層之折射率在從1.7至1.75的範圍中。
根據實施例,各半導體元件主要由III-V族化合物所製成。
根據實施例,各半導體元件主要包括氮化鎵。
根據實施例,各半導體元件之平均直徑在從200 nm至1 µm的範圍中。
根據實施例,密封(encapsulation)層包括由第一至少部分透明的材料所製成的基材(matrix)且具有散布於該基材中的第二材料之顆粒,第二材料之折射率大於第一材料之折射率。
根據實施例,第一材料為聚矽氧烷(polysiloxane)
根據實施例,第二材料為自二氧化鈦(TiO2
)、二氧化鋯(ZrO2
)及硫化鋅(ZnS)中所選出的介電材料。
根據實施例,密封層是由從包括下列的群組所選出的材料所製成:環氧聚合物(epoxide polymer)、SiOx
類型的矽氧化物、SiOy
Nz
類型的矽氧化物以及氧化鋁(Al2
O3
),其中x為大於0的實數且小於或等於2,其中y為大於0的實數且小於或等於2,且z大於0且小於或等於0.57。
根據實施例,發光二極體分布於該表面之一部分上,且在該部分上發光二極體之表面密度遠離該部分之邊緣而減少。
根據實施例,發光二極體分布於該表面之一部分上,且針對單位表面積該部分之周長對於該部分之表面積之比例大於或等於4。
根據實施例,該部分對應於具有孔的表面。
為了清楚起見,在各圖式中相同的元件已用相同的元件符號來指明,且此外,如同往常電子電路之表示,各圖式並未按比例繪製。此外,僅圖示及描述了有用於理解本揭示案的那些元件。特定而言,用於偏壓光電裝置之發光二極體的手段為習知且將不予描述。
在以下的描述中,除非另外指出,用語「實質上」、「近似」、及「在……的等級」意謂「在10%內」。此外,「主要由材料所形成的化合物」或「基於材料的化合物」意謂化合物包括該材料之大於或等於95%的比例,此比例較佳地大於99%。
本實施方式有關於具有三維元件的光電裝置,三維元件舉例而言,線型、圓錐形或錐形元件,特別是微米線或奈米線。
用語「微米線」或「奈米線」指明具有沿著選定方向拉長的形狀的三維結構,具有至少兩個尺度,稱作次要尺度,在從5 nm至2.5 µm的範圍中,較佳從50 nm至2.5 µm,以及第三尺度,稱作主要尺度,為至少等於該等次要尺度之最大者的1倍,較佳至少5倍,且更較佳至少10倍。在某些實施例中,次要尺度可能小於或等於近似1 µm,較佳在從100 nm至1 µm的範圍中,更較佳從100 nm至800 nm。在某些實施例中,各微米線或奈米線之高度可能大於或等於500 nm,較佳在從1 µm至50 µm的範圍中。
在以下的描述中,用語「線(wire)」用以意謂「微米線」或「奈米線」。較佳地,在與線之選定方向垂直的平面中,貫穿橫截面之重力中心的線之平均線為實質上直線形且以下稱作線之「軸(axis)」。
第1圖為具有發光二極體的光電裝置5之實施例之部分簡化橫截面視圖。
第1圖圖示結構,該結構從底部至頂部包括: 第一電極8: 半導體基板10,包括下表面11及上表面12,下表面11由第一電極8覆蓋,且上表面12至少於發光二極體之水平較佳為平面的; 晶種墊(seed pad)16,由提升線之生長的導電材料所製成且安置於表面12上; 高度H1的線20(圖示6條線),各線20與晶種墊16中之一者接觸,各線20包括高度H2的下部分22及高度H3的上部分24,下部分22與晶種墊16接觸,上部分24接續下部分22; 絕緣層26,在基板10之表面12上延伸且位於各線20之下部分22之側邊上; 殼28,包括半導體層之堆疊,該堆疊覆蓋各上部分24; 層30,形成覆蓋各殼28的第二電極且進一步在絕緣層26上延伸; 導電鏡層32,覆蓋在線20之間的電極層30而不在線20上延伸;及 密封層34,覆蓋整個結構及特別是電極30且包括前表面36。
光電裝置5可進一步包括螢光粉層,未圖示,提供在密封層34上或與密封層34重合。
由各線20、關聯的晶種墊16及殼28所形成的組件形成發光二極體DEL。二極體DEL之基底(base)對應至晶種墊16。殼28特定而言包括主動層,主動層為由發光二極體DEL所傳遞的大多數的電磁輻射從該層所發射的層。發光二極體DEL可以並聯連接且形成發光二極體之組件。組件可包括從數個發光二極體DEL至一千個發光二極體。
發光二極體DEL不在整個表面12上方形成是可能的。表面12上具有發光二極體形成在表面12上的該部分稱作主動區域(active area)。
基板10可對應至固態結構或對應至覆蓋由另一材料所製成的支撐件的層。基板10較佳為半導體基板,舉例而言,由矽所製成的基板、由鍺所製成的基板、由碳化矽所製成的基板、由III-V族化合物所製成的基板,例如GaN或GaAs或ZnO基板。較佳地,基板10為單晶矽基板。較佳地,基板10為與在微電子電路中實施的製造方法相容的半導體基板。基板10可對應於絕緣體上矽類型SOI之多層結構。
基板可被重摻雜、輕摻雜或未摻雜。在基板被重摻雜的情況下,半導體基板10可被摻雜以將電阻率降低至接近金屬之電阻率的電阻率,較佳地低於數個mohm.cm。基板10舉例而言為具有摻雜濃度在從5*1016
原子/cm3
至2*1020
原子/cm3
的範圍中的重摻雜基板。在基板為輕摻雜的情況下,舉例而言,可提供比起基板更加重摻雜的第一導電類型之摻雜區域或與第一類型相反的第二導電類型之摻雜區域,摻雜濃度小於或等於5*1016
原子/cm3
,較佳地實質上等於1015
原子/cm3
,該摻雜區域在基板10中自表面12在晶種墊16下延伸。在矽基板10的情況下,P型摻質之實例為硼(B)或銦(In)且N型摻質之實例為磷(P)、砷(As)或銻(Sb)。
矽基板10之表面12可為(100)表面。
晶種墊16,亦稱作晶種島,是由提升線20之生長的材料所製成。可提供處理以保護晶種墊之側邊及未被晶種墊覆蓋的基板部分之表面,以避免線在晶種墊之側邊上及在未被晶種墊覆蓋的基板部分之表面上生長。處理可包括在晶種墊之側邊上形成介電區域且在基板之頂上及/或內側延伸,而在介電區域上沒有線生長。作為變型,晶種墊16可由覆蓋基板10之表面12的晶種層所取代。然後介電區域可形成在晶種層上方,以避免在不欲區域中線之生長。
作為實例,形成晶種墊16的材料可為從元素週期表之第IV欄、第V欄或VI欄中過渡金屬之氮化物、碳化物或硼化物或這些化合物之組合。作為實例,晶種墊16可由下列所製成:氮化鋁(AlN)、硼(B)、氮化硼(BN)、鈦(Ti),氮化鈦(TiN)、鉭(Ta)、氮化鉭(TaN)、鉿(Hf)、氮化鉿(HfN)、鈮(Nb)、氮化鈮(NbN)、鋯(Zr)、二硼化鋯(ZrB2
)、氮化鋯(ZrN)、碳化矽(SiC)、鉭碳氮化物(TaCN)、以Mgx
Ny
形式的氮化鎂,其中x近似等於3且y近似等於2,舉例而言,以Mg3
N2
形式的氮化鎂或鎂氮化鎵(MgGaN)、鎢(W)、氮化鎢(WN),或上述之組合。
晶種墊16可用與基板10相同的導電類型來摻雜。
絕緣層26可由舉例而言二氧化矽(SiO2
)、氮化矽(Six
Ny
,其中x近似等於3且y近似等於4,舉例而言,Si3
N4
)、氮氧化矽(特別為通式SiOx
Ny
,舉例而言,Si2
ON2
)、氧化鋁(Al2
O3
)、二氧化鉿(HfO2
)或鑽石之介電材料所製成。作為實例,絕緣層26之厚度在從5 nm至500 nm的範圍內,舉例而言,等於近似30 nm。
線20為至少部分從至少一個半導體材料所形成。線20可為至少部分從主要包括III-V族化合物的半導體材料所形成,舉例而言,III-N族化合物。第III族元素之實例包括鎵(Ga)、銦(In)或鋁(Al)。III-N族化合物之實例為GaN、AlN、InN、InGaN、AlGaN或AlInGaN。亦可使用其他第V族元素,舉例而言,磷或砷。通常,在III-V族化合物中的元素可以不同莫耳分率結合。
線20可包括摻質。作為實例,對於III-V族化合物,摻質可選自包括第II族P型摻質的群組,舉例而言,鎂(Mg)、鋅(Zn)、鎘(Cd)或汞(Hg),及第IV族P型摻質的群組,舉例而言,碳(C),或第IV族N型摻質的群組,舉例而言,矽(Si)、鍺(Ge)、硒(Se)、硫(S)、鋱(Tb)或錫(Sn)。
線20之橫截面可具有不同形狀,例如,舉例而言,可為橢圓形、圓形或多邊形的形狀,特別是三角形、矩形、方形或六邊形。因此應理解,與線或沉積於此線上的層之橫截面有關而提及的用語「直徑」指明與在此橫截面中目標結構之表面積相關聯的量,對應至舉例而言與線橫截面具有相同表面積的碟之直徑。各線20之高度H1可在從250 nm至50 µm的範圍中。各線20沿著與表面12實質上垂直的軸可具有拉長的半導體結構。各線20可具有一般圓柱形形狀。兩線20之軸可距離從0.5 µm至10 µm,且較佳從1.5 µm至6 µm。作為實例,線20可規則地分布,特定而言,以六角形網狀(hexagonal network)分布。
作為實例,各線20之下部分22主要由III-N族化合物所形成,舉例而言,氮化鎵,與區域14相同的摻雜類型,舉例而言,N型,舉例而言,摻雜矽。下部分22沿著高度H2延伸,高度H2可在從100 nm至25 µm的範圍中。
作為實例,各線20之上部分24為至少部分由III-N族化合物所製成,舉例而言,GaN。上部分24可為N型摻雜,比起下部分22可能較不重摻雜,或不特意摻雜。上部分24沿著高度H3延伸,高度H3可在從100 nm至25 µm的範圍中。
殼28可包括複數個層之堆疊,特別包括: 主動層,覆蓋關聯的線20之上部分24; 中介層,具有與覆蓋主動層的下部分22之導電類型相反的導電類型;及 接合層,覆蓋中介層且由電極30所覆蓋。
主動層為由發光二極體DEL所傳遞的大多數輻射自該層發射的層。根據實例,主動層可包括侷限手段,例如多重量子井。多重量子井舉例而言由GaN層及InGaN層之交替所形成,GaN層及InGaN層分別具有從5 nm至20 nm(舉例而言,8 nm)的厚度及從1 nm至10 nm(舉例而言,2.5 nm)的厚度。GaN層可被摻雜,舉例而言,N型或P型。根據另一個實例,主動層可包括單一InGaN層,舉例而言,具有大於10 nm的厚度。
中介層,舉例而言,P型摻雜,可對應於半導體層或對應於半導體層之堆疊,且允許形成P-N接面或P-I-N接面,在P-N接面或P-I-N接面之中介P型層與上N型部分24之間包括主動層。
接合層可對應於半導體層或對應於半導體層之堆疊,且促使形成中介層與電極30之間的歐姆接點。作為實例,接合層可能以與各線20之下部分22之類型相反的類型非常重地摻雜,直到一或更多個半導體層之變性(degeneration),舉例而言,以濃度大於或等於1020
原子/cm3
的P型摻雜。
半導體層之堆疊可包括由三元合金所形成的電子障壁層,舉例而言,由與主動層及中介層接觸的氮化鋁鎵(AlGaN)或氮化鋁銦(AlInN)所製成,以提供在主動層中電子載體的良好分布。
電極30能夠偏壓各線20之主動層及能夠讓由發光二極體DEL所發射的電磁輻射通過。形成電極30的材料可為透明的且導電的材料,例如銦錫氧化物(ITO)、摻雜鋁的鋅氧化物,或石墨烯。作為實例,電極層30的厚度在從5 nm至200 nm的範圍中,較佳地從20 nm至50 nm的範圍中。
導電鏡層32較佳地對應於金屬層,舉例而言,由鋁、銀、銅或鋅所製成。作為實例,導電鏡層32的厚度在從20 nm至300 nm的範圍中,較佳地從100 nm至200 nm的範圍中。
密封層34由至少部分透明的絕緣材料所製成。密封層34之最大厚度大於線20之高度H1
。密封層34在線20之間延伸且覆蓋各線20。線20之間的空間完全填滿密封層34。密封層34之最大厚度在從250 nm至50 µm的範圍中,使得密封層34於發光二極體DEL之頂部處完全覆蓋電極30。
各發光二極體DEL之殼28之主動層在全部方向中發射光。
第2圖至第6圖繪示針對不同光發射配置由光束R所行進的路徑。在第2圖至第6圖中,並未圖示層30、層32及層34。將θ稱作由光束R相對於與線20之側壁垂直的方向D所形成的角度,且將θC
稱作組件之臨界全反射角,組件包括線20及殼28之主動層。
根據發射角θ,由殼28之主動層所發射的光可能耦合至輻射模式(radiated mode)稱作RL,如第2圖中所繪示,或耦合至波導模式(guided mode)稱作GL,如第3圖中所繪示。波導模式GL具有大於臨界全反射角θC的發射角θ且沿著線20以鋸齒狀的方式傳播。相反地,輻射模式RL具有小於臨界全反射角θC的發射角θ,且在密封層34中完全穿透。
臨界全反射角θC是由司乃耳定律(Snell’s law)根據以下關係式(1)所提供: θC
=asin(nencap
/nwire
) (1) 其中nencap
為密封層34之光學折射率之實部(real part)且nwire
為線20及線20的殼28之光學折射率之實部,nwire
大於nencap
。
光學折射率為表徵介質之光學性質的無因次數,特別表徵吸收及擴散。折射率等於複數光學指數(complex optical index)之實部。舉例而言折射率可由橢圓偏光儀(ellipsometry)所決定。
在入射角θ下,波導模式GL分解成迷失在基板中的模式SGL(第4圖)、成為反射模式RGL(第5圖)及穿透模式TGL(第6圖)。模式SGL導引至線20之基部且迷失在基板10中。模式TGL於線20之上表面處具有小於臨界全反射角的入射角,且因此在密封層34中穿透。模式RGL於上表面處處於全反射條件且傳送返回朝向線20之基部而不被提取。
在波導模式GL中,僅有穿透波導模式TGL參與由觀看者所察覺到的光。導向基板的模式SGL直接迷失且反射模式RGL保持被捕捉於線20內直到它們在基板10中被吸收或迷失。
第7圖圖示根據密封層34之折射率nencap
,模式RL、GL、SGL、RGL及TGL之比例。從發光二極體所提取的光之比例為比例RL及比例TGL之和。
第8圖圖示根據密封層34之折射率nencap
,對應於相對於波導模式GL之總數的波導模式RGL之比例的變化曲線CRGL。第7圖之曲線及第8圖之曲線是在具有800 nm的平均直徑的六角形橫截面的GaN線及具有275 nm厚度的殼的情況下所獲得。
當密封層34之折射率增加時,輻射模式RL之比例增加而波導模式GL之比例減少。此外,針對密封層34之折射率等於近似1.73時,被捕捉的波導光RGL之比例減少變成零。
藉由模擬,本發明人已表明模式RL、GL、SGL、RGL及TGL之比例之變化之曲線之形狀為實質上相同而與線20之平均直徑無關,只要線20之平均直徑大於200 nm。特定而言,於傳播模式RGL消除下的折射率實質上與線20之平均直徑無關,只要線20之平均直徑大於200 nm。
為了讓觀看光電裝置5的觀看者所察覺到,光應該經由前表面36離開密封層。表面36可對應於自由表面,亦即,與空氣接觸。密封層34之折射率與空氣之折射率之間的差越大,相對於與表面36垂直的方向所測量到的臨界全反射角越低,亦即,源自發光二極體DEL傾向在表面36上反射的光越多。因此,不希望密封層34之折射率太高。
當形成線及主動層的材料為III-V族化合物時,本發明人已藉由模擬表明與密封層34之折射率所能獲得的最佳妥協為在從1.7至1.75的範圍中,較佳在從1.72至1.74的範圍中,更較佳近似1.73。
較佳地,線20之平均直徑在從200 nm至1 µm的範圍中,較佳從300 nm至800 nm。
密封層34可包括至少部分透明的無機材料之基材且具有可能散布於該基材中的介電材料之顆粒。形成顆粒的介電材料之折射率大於形成基材的材料之折射率。根據實例,密封層34包括由矽氧烷(silicone)亦稱為聚矽氧烷(polysiloxane)所製成的基材,且進一步包括散布於該基材中的介電材料之顆粒。該等顆粒是由提供具有適應折射率的相對球狀奈米範圍顆粒的任何類型的材料所製成。作為實例,顆粒可由二氧化鈦(TiO2
)、二氧化鋯(ZrO2
)、硫化鋅(ZnS)、硫化鉛(PbS)或非晶矽(Si)所製成。顆粒之平均直徑界定為相同體積的球體之直徑。介電材料之顆粒之平均直徑在從2 nm至250 nm的範圍中。相關於密封層34之整體重量,顆粒之體積濃度在從1%至50%的範圍中。
根據另一個實施例,無機材料是從包括下列的群組所選出:環氧聚合物(epoxide polymer)、SiOx
類型的矽氧化物(其中x為大於0的實數且小於或等於2)、SiOy
Nz
類型的矽氧化物(其中y為大於0的實數且小於或等於2,且z大於0且小於或等於0.57)及氧化鋁(Al2
O3
)。
密封層34可由至少部分透明的有機材料所製成。根據實例,密封層34由聚亞醯胺(polyimide)所製成。根據另一個實例,密封層34由環氧聚合物所製成,環氧聚合物進一步包括分布於基材中的介電材料之顆粒。該等顆粒可由二氧化鈦(TiO2
)、二氧化鋯(ZrO2
)、硫化鋅(ZnS)、硫化鉛(PbS)或非晶矽(Si)所製成。
為了改善光電裝置5之提取效率,表面處理,稱作粗糙化(texturing),可施加至密封層34之表面36以在表面36上形成凸起的區域。針對由無機材料所製成的密封層34,使表面36粗糙化之方法可包括可能在保護表面36待處理之部分的遮罩存在的情況下化學蝕刻之步驟或機械磨耗之步驟,以提升在表面處圖案之形成。針對由有機材料所製成的層34,使表面36粗糙化之方法可包括壓花(embossing)、模製(moulding)等。
為了改善光電裝置5之提取效率,密封層34可由至少部分透明的額外層所覆蓋。然後該額外層之折射率介於密封層34之折射率與空氣之折射率之間。作為變型,至少兩層之堆疊可覆蓋密封層34。在該堆疊中該等層之折射率以從與密封層34接觸的該堆疊之第一層至與空氣接觸的該堆疊之最後一層的方式減少,第一層之折射率小於密封層34之折射率,且最後一層之折射率大於空氣之折射率。
根據前述實施例的光電裝置促使有利地增加光電裝置之全體的提取效率,亦即,整個表面36各處測量到的效率。
提取效率可局部地測量,亦即,針對表面36之一部分。然後,該局部提取效率對應於經由考量的部分從光電裝置逃脫的光量對於由該部分之發光二極體所傳遞的光量之比例。希望在整個表面36上的局部提取效率之變化越低越好,以避免觀看者當觀看光電裝置5時察覺亮度差異。
第9圖為光電裝置50之實例之頂視圖,包括第1圖中所示的光電裝置5之全部元件且具有規則地分布於光電裝置5中的發光二極體DEL,舉例而言,以成列及成行分布在方形主動區域51上。主動區域51之側邊緣標記為元件符號52且主動區域51之角落標記為元件符號54。各發光二極體示意圖示為一個點。作為實例,除了沿著邊緣52坐落的二極體之外,各發光二極體DEL坐落於方形之中心處,該方形包括於各頂點處的發光二極體及在各邊緣之中間的發光二極體。
在第9圖所示的實例中,每表面積單位的發光二極體之密度在整個主動區域51上為實質上定值。作為實例,發光二極體之表面密度為實質上定值且在從4*106
/cm2
至3*107
/cm2
的範圍中。
第10圖圖示第9圖之光電裝置50之局部提取效率在四分之一的主動區域51上的變化。第10圖之曲線是在六角形橫截面的GaN奈米線之陣列的情況下獲得,兩個奈米線之軸之間的距離為殼28之平均半徑的3倍且密封層34之材料之折射率等於1.75。
比起主動區域51之中心,沿著邊緣52的局部提取效率較高。此外,比起在主動區域51之邊緣52上,在頂點54處的局部提取效率較高。此現象之解釋為發光二極體之接近的鄰居之數目越大,由此發光二極體所發射的光束撞擊鄰近的發光二極體中之一者且被該等鄰居吸收或捕捉的機率越高。
藉由模擬,本發明人已表明提取效率降低,只要兩個相鄰發光二極體之軸之間的距離小於殼28之平均半徑的15倍。
針對相鄰發光二極體之軸之間的距離小於殼28之平均半徑的15倍,已觀察到當列及行之數目大於近似50時,主動區域51之中心之提取效率達到最小值而與列及行之數目無關。
第11圖為與第9圖非常類似的光電裝置60之實施例。光電裝置60包括光電裝置50之全部的元件,差異在於每表面積單位的發光二極體之密度從裝置之中心一路朝向邊緣52逐漸增加。更特定而言,在主動區域51之中心處的發光二極體之表面密度小於沿著邊緣52的發光二極體之表面密度。此外,沿著邊緣52的發光二極體之表面密度小於主動區域51之頂點54處的發光二極體之表面密度。
作為實例,發光二極體之表面密度之變化可對應於例如第10圖中所圖示的提取效率之變化之倒數。作為實例,在光電裝置之主動區域之中心處的發光二極體之表面密度可在從2*106
/cm2
至6*106
/cm2
的範圍中,而沿著光電裝置之主動區域之邊緣的發光二極體之表面密度可在從7*106
/cm2
至2*107
/cm2
的範圍中。
根據另一個實施例,本發明人已表明提取效率之均勻性可藉由增加主動區域之周長對於主動區域之表面之比例來改善。較佳地,針對單位主動表面積,主動區域之周長對於表面之比例P/A大於4,較佳地大於或等於4.5,更較佳地大於或等於5,且特定而言大於或等於6。
第12圖至第20圖圖示光電裝置之實施例之簡化頂視圖,針對該等光電裝置之各者僅圖示主動區域之輪廓。對於這些實例之各者,主動區域之周長對於主動區域之表面積之比例大於針對相同表面積的方形所獲得的比例。
在第12圖中,主動區域70具有環型,包括方形外邊緣72及方形內邊緣74。在第13圖中,主動區域76包括一個或多於一個的矩形區域78,圖示兩個矩形區域。在第14圖中,主動區域80包括一個或多於一個的具有波浪狀邊緣的帶(strip)82,圖示兩條帶82。在第15圖中,主動區域84具有三角形形狀。在第16圖中,主動區域86為星形的。在第17圖中,主動區域88包括星形的外邊緣90及星形的內邊緣91。有利地,主動區域之外周長及可能內周長遵循接近不規則碎片形曲線的曲線。在第18圖、第19圖及第20圖中,主動區域94、96及98在兩次、三次或四次迭代之後分別具有科赫(Koch)雪片的形狀。對於主動區域94、96及98,主動區域之單位表面積的比例P/A分別為6.4、8.5及11.4。第12圖及第17圖圖示對應於具有孔(hole)的表面的主動區域之實例。
提供光電裝置5之製造方法之實施例,包括以下步驟:
(1)在基板10之表面12上形成晶種墊16。
晶種墊16可藉由在表面12上沉積晶種層且藉由蝕刻晶種層之部分一路至基板10之表面12以劃定晶種墊的方式來獲得。晶種層可藉由例如化學氣相沉積(CVD)或有機金屬化學氣相沉積(MOCVD)的方法來沉積,有機金屬化學氣相沉積亦稱作有機金屬氣相磊晶(MOVPE)。然而,可使用例如分子束磊晶(MBE)、氣源MBE(GSMBE)、有機金屬MBE(MOMBE)、電漿輔助MBE(PAMBE)、原子層磊晶(ALE)、氫化物氣相磊晶(HVPE)的方法,以及原子層沉積(ALD)的方法。此外,可使用例如蒸鍍或反應性陰極濺射的方法。
當晶種墊16由氮化鋁所製成時,晶種墊16可實質上經粗糙化且具有較佳的極性。晶種墊16之粗糙化可藉由在沉積晶種層之後實行額外處理來獲得。舉例而言,該額外處理為在氨流(NH3
)下進行退火。
(2)保護基板10之表面12之不被晶種墊16所覆蓋的部分,以避免在這些部分上後續線之生長。此舉可藉由氮化步驟來獲得,氮化步驟導致於基板10之表面處在晶種墊16之間形成氮化矽區域(舉例而言,SiN或Si3
N4
)。此舉可藉由遮蔽晶種墊16之間的基板10之步驟來獲得,包含層之沉積,舉例而言SiO2
或SiN或Si3
N4
介電質之層,且然後在微影步驟之後蝕刻晶種墊16之外側的該層。在此情況下,遮罩層可在晶種墊16上方延伸。當藉由遮蔽基板10之步驟來執行保護步驟(2)時,可避免晶種層蝕刻步驟。然後晶種墊16由具有在線交會處讓均勻連續層之表面保持自由的均勻連續層所形成。
(3)沿著高度H2
生長各線20之下部分22。各線20從位於下方的晶種墊16之頂部生長。
線20可由CVD、MOCVD、MBE、GSMBE、PAMBE、ALE、HVPE、ALD類型之處理來生長。此外,可使用電化學處理,舉例而言,化學浴沉積(CBD)、水熱(hydrothermal)處理、液態氣溶膠熱解(liquid aerosol pyrolysis)或電沉積(electrodeposition)。
作為實例,線生長方法可包括注入第III族元素之前驅物及第V族元素之前驅物到反應器中。第III族元素之前驅物之實例為三甲基鎵(trimethylgallium; TMGa)、三乙基鎵(triethylgallium; TEGa)、三甲基銦(trimethylindium; TMIn)或三甲基鋁(trimethylaluminum; TMAl)。第V族元素之前驅物之實例為氨(NH3
)、三丁基磷化氫(tertiarybutylphosphine; TBP)、三氫化砷(AsH3
)或偏二甲肼(unsymmetrical dimethylhydrazine; UDMH)。
根據本發明之實施例,在III-V族化合物之線之生長之第一階段,除了III-V族化合物之前驅物之外,過量添加額外元素之前驅物。額外元素可為矽(Si)。矽之前驅物之實例為矽烷(SiH4
)。
在前驅物氣體中矽烷之存在導致將矽引入GaN化合物。因此獲得較低N型摻雜部分22。此進一步轉換為形成矽氮化物層,未圖示,當部分22生長時,矽氮化物層覆蓋高度H2
的部分22之周圍,除了頂部之外。
(4)在下部分22之頂部上生長各線20之具有高度H3的上部分24。針對上部分24之生長,作為實例,維持先前所述MOCVD反應器之操作條件,但事實上減少反應器中矽烷流,舉例而言,以大於或等於10的因子減少,或停止。即使當矽烷流停止時,由於在此主動部分源自相鄰鈍化部分的摻質之擴散,或由於GaN之殘留摻雜,上部分24可被N型摻雜。
(5)形成絕緣層26,舉例而言,藉由於步驟(4)處所獲得的整個結構上方保形沉積絕緣層,及蝕刻此層以曝露各線20之上部分24。
(6)對於各線20,藉由磊晶形成用以形成殼28的層。已知覆蓋下部分22之周圍的絕緣層26存在,形成殼28的層之沉積僅在線20之未被絕緣層26覆蓋的上部分24上發生。
(7)形成電極30,舉例而言,藉由保形沉積。
(8)形成導電鏡層32,舉例而言,藉由於步驟(7)處所獲得的整個結構上方進行物理氣相沉積(PVD),或舉例而言,藉由蒸鍍或藉由陰極濺射及蝕刻此層以曝露各線20。
(9)形成密封層34。當密封層34由矽氧烷所製成時,密封層34可藉由旋轉塗佈沉積方法來沉積,藉由噴墨印刷方法來沉積,或藉由絲網(silk-screening)方法來沉積。當密封層34為氧化物時,密封層34可藉由CVD來沉積。
並且(10)鋸切基板10以分離光電裝置。
在前述的實施例中,絕緣層26覆蓋各線20之下部分22之整個周圍。作為變型,針對下部分22之部分可能不被絕緣層26所覆蓋。在此情況下,絕緣層26覆蓋線20達小於H2
的高度且殼28覆蓋線20達大於H3
的高度。層26可能不覆蓋各線20之下部分22。在此情況下,殼28可覆蓋各線20達高度H1
。
在前述的實施例中,絕緣層26不覆蓋各線20之上部分24之周圍。作為變型,絕緣層26可覆蓋各線20之上部分24之一部分。在此情況下,絕緣層26覆蓋線20達大於H2
的高度且殼28覆蓋線20達小於H3
的高度。
根據另一種變型,對於各線20,絕緣層26可部分覆蓋殼30之下部分。
根據先前所述製造方法之變型,於絕緣層26在整個線20上方或僅在線20之一部分上方之前,可形成用以形成殼28的層,舉例而言,上部分24。
已描述本發明之具體實施例。本領域熟知技藝者將想到各種變更及修改。此外,雖然在先前所述實施例中,各線20在線之基部與晶種墊16中之一者接觸之處包括鈍化部分22,但可不存在鈍化部分22。
此外,雖然已針對殼28覆蓋關聯的線20之頂部及線20之側邊之一部分的光電裝置描述實施例,可能僅於線20之頂部處提供殼。
在此以上已描述具有不同變型的各種實施例。應注意到,本領域熟知技藝者可結合這些各種實施例及變型之各種元件而不表明任何進步性。特定而言,包括具有在從1.7至1.75的範圍中的折射率的密封層的光電裝置可進一步包括可變的發光二極體之表面密度,舉例而言,圖示於第11圖中。此外,包括具有在從1.7至1.75的範圍中的折射率的密封層的光電裝置可進一步包括主動區域之周長對於表面積之比例,該比例大於針對方形主動區域所獲得的比例,舉例而言如先前關於第12圖至第20圖所述。此外,具有大於針對方形主動區域所獲得的比例的主動區域之周長對於表面積之比例的光電裝置可進一步包括可變的發光二極體之表面密度。
5‧‧‧光電裝置8‧‧‧第一電極10‧‧‧半導體基板11‧‧‧下表面12‧‧‧上表面16‧‧‧晶種墊20‧‧‧半導體元件/線22‧‧‧下部分24‧‧‧上部分26‧‧‧絕緣層28‧‧‧殼30‧‧‧層/電極層/電極32‧‧‧導電鏡層34‧‧‧密封層36‧‧‧前表面50‧‧‧光電裝置51‧‧‧主動區域52‧‧‧主動區域之側邊緣54‧‧‧主動區域之角落/頂點60‧‧‧光電裝置70‧‧‧主動區域72‧‧‧方形外邊緣74‧‧‧方形內邊緣76‧‧‧主動區域78‧‧‧矩形區域80‧‧‧主動區域82‧‧‧帶84‧‧‧主動區域86‧‧‧主動區域88‧‧‧主動區域90‧‧‧星形的外邊緣91‧‧‧星形的內邊緣94‧‧‧主動區域96‧‧‧主動區域98‧‧‧主動區域CRGL‧‧‧曲線D‧‧‧方向DEL‧‧‧發光二極體GL‧‧‧波導模式H1‧‧‧高度H2‧‧‧高度H3‧‧‧高度R‧‧‧光束RL‧‧‧輻射模式RGL‧‧‧反射波導模式SGL‧‧‧迷失在基板中的波導模式TGL‧‧‧穿透波導模式θ‧‧‧發射角θC‧‧‧臨界全反射角
前述及其他特徵及優點將在以下關聯附圖的具體實施例之非限制描述中詳細討論,圖式當中:
第1圖為具有微米線或奈米線的光電裝置之實施例之部分簡化橫截面視圖;
第2圖至第6圖繪示在微米線或奈米線中由光束所遵循的路徑之不同配置;
第7圖圖示根據環繞發光二極體的材料之折射率,由具有微米線或奈米線的發光二極體所傳遞的光之傳播模式之分布之變化;
第8圖圖示根據環繞發光二極體的材料之折射率,在微米線或奈米線的發光二極體中捕捉的光導模式之傳播之變化之曲線;
第9圖為包括具有微米線或奈米線的發光二極體的光電裝置之部分簡化頂面視圖;
第10圖圖示根據在第9圖之光電裝置之前表面上考量的位置,提取效率之變化;及
第11圖至第20圖為包括具有微米線或奈米線的發光二極體的光電裝置之實施例之部分簡化頂面視圖。
國內寄存資訊 (請依寄存機構、日期、號碼順序註記) 無
國外寄存資訊 (請依寄存國家、機構、日期、號碼順序註記) 無
5‧‧‧光電裝置
8‧‧‧第一電極
10‧‧‧半導體基板
11‧‧‧下表面
12‧‧‧上表面
16‧‧‧晶種墊
20‧‧‧半導體元件/線
22‧‧‧下部分
24‧‧‧上部分
26‧‧‧絕緣層
28‧‧‧殼
30‧‧‧層/電極層/電極
32‧‧‧導電鏡層
34‧‧‧密封層
36‧‧‧前表面
DEL‧‧‧發光二極體
H1‧‧‧高度
H2‧‧‧高度
H3‧‧‧高度
Claims (6)
- 一種光電裝置(5),包括:一半導體基板(10),該半導體基板(10)具有一表面(12);以及由該表面所支撐的發光二極體(DEL),該等發光二極體(DEL)包括線型、圓錐形或錐形的半導體元件(20),其中該等發光二極體(DEL)分布於該表面(12)之一部分(70;76;80;84;86;88;94;96;98)上方,且其中針對一單位表面積該部分之周長對於該部分之表面積之比例大於或等於4。
- 如請求項1所述之光電裝置,其中該部分(70;90)對應於具有一孔的一表面。
- 如請求項1所述之光電裝置,其中該等發光二極體(DEL)分布於該表面(12)之一部分(51)上方,且該等發光二極體(DEL)在該部分上之表面密度遠離該部分之邊緣(52)而減少。
- 如請求項1所述之光電裝置,其中各半導體元件(20)主要由III-V族化合物所製成。
- 如請求項4所述之光電裝置,其中各半導體元件(20)主要包括氮化鎵。
- 如請求項1所述之光電裝置,其中各半導體 元件(20)之平均直徑在從200nm至1μm的範圍中。
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FR3015772B1 (fr) * | 2013-12-19 | 2017-10-13 | Aledia | Dispositif optoelectronique a diodes electroluminescentes a extraction de lumiere amelioree |
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2013
- 2013-12-19 FR FR1363005A patent/FR3015772B1/fr not_active Expired - Fee Related
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2014
- 2014-12-11 WO PCT/EP2014/077418 patent/WO2015091212A1/fr active Application Filing
- 2014-12-11 EP EP14812451.4A patent/EP3084846B1/fr active Active
- 2014-12-11 CN CN201480069520.6A patent/CN106415858B/zh active Active
- 2014-12-11 JP JP2016539256A patent/JP6605472B2/ja active Active
- 2014-12-11 EP EP18169640.2A patent/EP3373345B1/fr active Active
- 2014-12-11 US US15/101,887 patent/US9601543B2/en active Active
- 2014-12-11 KR KR1020167016858A patent/KR102279462B1/ko active IP Right Grant
- 2014-12-11 EP EP18169638.6A patent/EP3373344B1/fr active Active
- 2014-12-16 TW TW108135841A patent/TWI761708B/zh active
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2017
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2019
- 2019-06-18 JP JP2019113055A patent/JP2019169735A/ja active Pending
- 2019-06-18 JP JP2019113054A patent/JP6893954B2/ja active Active
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Publication number | Publication date |
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US10177288B2 (en) | 2019-01-08 |
TW201921736A (zh) | 2019-06-01 |
US20170148960A1 (en) | 2017-05-25 |
US9601543B2 (en) | 2017-03-21 |
FR3015772A1 (fr) | 2015-06-26 |
US10062818B2 (en) | 2018-08-28 |
JP6893954B2 (ja) | 2021-06-23 |
TW202005123A (zh) | 2020-01-16 |
TWI761708B (zh) | 2022-04-21 |
EP3373345A1 (fr) | 2018-09-12 |
JP2019169735A (ja) | 2019-10-03 |
EP3084846B1 (fr) | 2018-07-11 |
US20160307960A1 (en) | 2016-10-20 |
TWI656666B (zh) | 2019-04-11 |
EP3373344B1 (fr) | 2021-03-17 |
JP2017501573A (ja) | 2017-01-12 |
CN106415858B (zh) | 2019-04-23 |
FR3015772B1 (fr) | 2017-10-13 |
TW201535801A (zh) | 2015-09-16 |
JP2019195077A (ja) | 2019-11-07 |
KR20160100983A (ko) | 2016-08-24 |
WO2015091212A1 (fr) | 2015-06-25 |
JP6605472B2 (ja) | 2019-11-13 |
CN106415858A (zh) | 2017-02-15 |
EP3373345B1 (fr) | 2021-09-15 |
EP3084846A1 (fr) | 2016-10-26 |
KR102279462B1 (ko) | 2021-07-19 |
EP3373344A1 (fr) | 2018-09-12 |
US20180219143A1 (en) | 2018-08-02 |
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