TW201331985A - Etching method of organic substance layer - Google Patents

Etching method of organic substance layer Download PDF

Info

Publication number
TW201331985A
TW201331985A TW101110048A TW101110048A TW201331985A TW 201331985 A TW201331985 A TW 201331985A TW 101110048 A TW101110048 A TW 101110048A TW 101110048 A TW101110048 A TW 101110048A TW 201331985 A TW201331985 A TW 201331985A
Authority
TW
Taiwan
Prior art keywords
gas
etching
layer
organic
material layer
Prior art date
Application number
TW101110048A
Other languages
Chinese (zh)
Other versions
TWI533354B (en
Inventor
Kevin Pears
Original Assignee
Advanced Micro Fab Equip Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Advanced Micro Fab Equip Inc filed Critical Advanced Micro Fab Equip Inc
Publication of TW201331985A publication Critical patent/TW201331985A/en
Application granted granted Critical
Publication of TWI533354B publication Critical patent/TWI533354B/en

Links

Landscapes

  • Drying Of Semiconductors (AREA)

Abstract

An etching method of organic substance layer, such as a bottom photo resist material layer, is provided. The mentioned etching method includes: placing a substrate to be etched into a plasma reaction chamber, wherein the mentioned substrate comprises thereon an etching target organic substance material layer; directing reaction gas into the plasma reaction chamber; exerting the radiofrequency electrical energy onto the reaction gas to ignite the plasma body to perform the etching towards the mentioned substrate; wherein the mentioned reaction gas comprises main etching gas, dilution gas, and sidewall protection gas, in which the main etching gas molecule is O2, the dilution gas is selected from one of the Ar, N2, or CO, or the mixture of the mentioned gases, and the sidewall protection gas is COS. The flow rate of the dilution gas is greater than that of the mentioned main etching gas, while the flow rate of the sidewall protection gas is smaller than that of the main etching gas.

Description

有機物層刻蝕方法 Organic layer etching method

本發明關於一種有機物層的等離子刻蝕方法,特別關於一種在低臨界尺寸(critical dimension,CD)要求下的有機物層的刻蝕方法。 The present invention relates to a plasma etching method for an organic layer, and more particularly to an etching method for an organic layer under a low critical dimension (CD) requirement.

在半導體器件製造領域內,利用等離子來進行加工的各種反應腔普遍存在。隨著加工精度越來越高,臨界尺寸(critical dimension)越來越小,現在業界的臨界尺寸已經達到了45 nm以下,如22 nm的CPU已經面世。而現有的通過光學方法對光刻膠進行照射來獲得加工圖形的方法最小臨界尺寸僅能達到45 nm左右,要獲得更高精度的光刻機,以獲得低尺寸圖形要付出巨大代價,不具有經濟價值。為了在現有光刻技術條件下獲得更小臨界尺寸的加工能力,現有技術廣泛採用了臨界尺寸縮小技術,即在較大掩膜的基礎上通過刻蝕形成具有梯形剖面的孔洞或溝槽,最終獲得具有較小臨界尺寸的掩膜。採用這一技術的關鍵是獲得可以精確控制刻蝕結果的方法,使得刻蝕過程中圖形尺寸能夠均勻的縮小,且不會變形造成最終圖形轉換失真。採用這樣的臨界尺寸縮小技術可以應用到多種材料層的刻蝕,如絕緣材料層,通常是含矽的無機物如APL、SiO2、SiN等。這些材料層相對比較堅硬比較容易控制刻蝕形成的溝道形狀。但是為了減少加工步驟直接獲得高精度的圖形化掩膜,現在也有在傳統光刻膠下方添加一層較厚有機物材 料層,通過刻蝕直接形成低臨界尺寸掩膜的方法。在這樣的材料層上刻蝕難度就要大的多,因為這些材料層與光刻膠類似,是較軟的有機物材料層,所以也叫底層光刻膠(bottom photo resist,BPR)。在刻蝕中這些材料層的側壁很容易被破壞形成缺口造成圖形失真。現有刻蝕方法往往採用HBr/O2、CO/O2、N2/H2等刻蝕氣體來對這些BPR層進行刻蝕,但是用這些氣體以及配套的刻蝕工藝很難獲得精確的刻蝕圖形。所以業界需要一種能夠對這種有機物材料層進行精確刻蝕以形成低臨界尺寸圖形的刻蝕方法。 In the field of semiconductor device fabrication, various reaction chambers that utilize plasma for processing are ubiquitous. With higher processing precision and smaller critical dimensions, the industry's critical dimensions have now reached below 45 nm, such as the 22 nm CPU. However, the existing method for obtaining a processed pattern by optically irradiating the photoresist can achieve a minimum critical dimension of only about 45 nm, and a higher precision lithography machine is required to obtain a low-size graphic, which has a great cost, and does not have Economic Value. In order to obtain a smaller critical dimension processing capability under the existing lithography technology, the prior art widely adopts a critical dimension reduction technique, that is, forming a hole or a groove having a trapezoidal profile by etching on the basis of a large mask, and finally A mask with a smaller critical dimension is obtained. The key to adopting this technology is to obtain a method that can accurately control the etching result, so that the pattern size can be uniformly reduced during the etching process, and the final pattern conversion distortion is not deformed. Such a critical dimension reduction technique can be applied to etching of a plurality of material layers, such as an insulating material layer, usually a germanium-containing inorganic substance such as APL, SiO2, SiN, or the like. These material layers are relatively hard to control the shape of the channel formed by etching. However, in order to reduce the processing steps and directly obtain a high-precision patterned mask, it is now also possible to add a thicker organic material under the conventional photoresist. Material layer, a method of directly forming a low critical size mask by etching. It is much more difficult to etch on such a material layer because these material layers are similar to photoresist and are softer organic material layers, so they are also called bottom photo resist (BPR). The sidewalls of these material layers are easily broken during etching to form a gap causing pattern distortion. Existing etching methods often use etching gases such as HBr/O2, CO/O2, and N2/H2 to etch these BPR layers, but it is difficult to obtain accurate etching patterns using these gases and associated etching processes. Therefore, there is a need in the industry for an etching method that can precisely etch such an organic material layer to form a low critical dimension pattern.

本發明的發明內容只提供一個對本發明部分方面和特點的基本理解,其不是對本發明的廣泛的概述,也不是用來特別指出本發明關鍵的要素或者勾畫發明的範圍。其唯一的目的是簡化地呈現本發明的一些概念,為後續詳細的描述本發明作一些鋪墊。 The summary of the present invention is intended to provide a basic understanding of the invention, and is not intended to Its sole purpose is to present some concepts of the invention in a simplified

本發明揭露了一種有機物層刻蝕方法,所述刻蝕方法包括:將待刻蝕基片放入等離子反應腔,所述基片上包括刻蝕目標有機物材料層;通入反應氣體到等離子反應腔;向反應氣體施加射頻電能點燃等離子體,對所述基片進行刻蝕;其中所述反應氣體包括主刻蝕氣體、稀釋氣體和側壁保護氣體,其中主刻蝕氣體分子為O2,稀釋氣體選自Ar、N2、CO之一或者這三者的混合物,側壁保護氣體為COS,稀釋氣體流量大於所述主刻蝕氣體流量,側壁保護氣體流量小於主刻蝕氣體流量。其中所述刻蝕目標材 料層包括一層有機物掩膜材料層,以及位於該有機物掩膜材料層上方圖形化的無機材料層,所述圖形化無機材料層具有第一臨界尺寸。其中所述圖形化無機材料層的圖形通過位於其上方的具有第一臨界尺寸圖形的光刻膠為掩膜刻蝕獲得。所述有機物掩膜材料層通過刻蝕在材料層底部形成具有第二臨界尺寸的圖形,其中第二臨界尺寸小於第一臨界尺寸。並且以具有第二臨界尺寸圖形的所述有機物掩膜材料層為掩膜刻蝕下方的第二無機材料層。其中所述反應腔中通入反應氣體中稀釋氣體與主刻蝕氣體O2的流量比可以為5:1~10:1,也可以是5:1~8:1。其中所述反應腔中通入反應氣體中稀釋氣體的流量與側壁保護氣體COS的流量比可以在20:1到6:1之間。 The invention discloses an organic layer etching method. The etching method comprises: placing a substrate to be etched into a plasma reaction chamber, wherein the substrate comprises etching a target organic material layer; and introducing a reaction gas into the plasma reaction chamber. Applying radio frequency electric energy to the reaction gas to ignite the plasma, and etching the substrate; wherein the reaction gas includes a main etching gas, a diluent gas, and a sidewall shielding gas, wherein the main etching gas molecule is O2, and the diluent gas is selected From one of Ar, N2, CO or a mixture of the three, the sidewall shielding gas is COS, the dilution gas flow rate is greater than the main etching gas flow rate, and the sidewall shielding gas flow rate is smaller than the main etching gas flow rate. The etching target material The layer includes a layer of organic mask material and a layer of inorganic material patterned over the layer of organic mask material, the patterned layer of inorganic material having a first critical dimension. Wherein the pattern of the patterned inorganic material layer is obtained by mask etching of a photoresist having a first critical dimension pattern located thereon. The organic mask material layer forms a pattern having a second critical dimension at the bottom of the material layer by etching, wherein the second critical dimension is smaller than the first critical dimension. And etching the underlying second inorganic material layer with the organic mask material layer having the second critical dimension pattern as a mask. The flow ratio of the dilution gas to the main etching gas O2 in the reaction gas in the reaction chamber may be 5:1 to 10:1, or 5:1 to 8:1. The ratio of the flow rate of the diluent gas in the reaction gas to the side wall shielding gas COS in the reaction chamber may be between 20:1 and 6:1.

根據本發明一個實施例,其中所述有機物掩膜材料層厚度大於100nm。所述射頻電能施加為100-1000W的射頻電能,刻蝕時間持續大於30秒。 According to an embodiment of the invention, the organic mask material layer has a thickness greater than 100 nm. The radio frequency power is applied as 100-1000 W of radio frequency power, and the etching time lasts for more than 30 seconds.

通過閱讀參照附圖對非限制性實施例所作的詳細描述,本發明的其他特徵、目的和優點將會變得更明顯:附圖構成了本說明書的一部分,和說明書一起列舉了不同的實施例,以解釋和闡明本發明的宗旨。附圖並沒有描繪出具體實施例的所有技術特徵,也沒有描繪出部件的實際大小和真實比例。 Other features, objects, and advantages of the present invention will become more apparent from To explain and clarify the gist of the present invention. The drawings do not depict all of the technical features of the specific embodiments, nor the actual size and true proportions of the components.

本發明實施例提供一種對施加到等離子處理腔的射頻功率進行控制的系統和方法,以實現最小化反射功率並有效地將射頻功率施加到等離子中。各種實施例都 在不需要修改驗證過的技術選單的情況下實現自動調節射頻功率。這一自動調節可以用調節頻率匹配的和射頻匹配網路參數的方式來實現。 Embodiments of the present invention provide a system and method for controlling radio frequency power applied to a plasma processing chamber to minimize reflected power and effectively apply radio frequency power to the plasma. Various embodiments Automatic adjustment of RF power without the need to modify the validated technology menu. This automatic adjustment can be accomplished by adjusting the frequency matching and RF matching network parameters.

圖1顯示了一個本發明刻蝕進行的等離子反應腔1。該反應腔1包括基座33,基座33上連接有射頻電源。其中基座33也作為下電極連接有低頻的射頻功率,在等離子點燃後通過調節該低頻射頻電源的功率來調節等離子的能量大小。基座33上包括基片固定裝置34,該基片固定裝置34可以是靜電夾盤或者機械夾盤等裝置。待加工基片30固定在基片固定裝置34上方。基片30週邊還包括一個邊緣環36,以實現對基片邊緣位置溫度,電場分佈等的控制,還能保護下方器件不被反應腔中點燃的等離子腐蝕。反應腔頂部與基座相對的位置還包括一氣體擴散裝置40,連接一氣源50,該氣體擴散裝置可以是常用的氣體噴淋頭也可以是其他氣體噴頭。除了圖1中所示的電容耦合型(CCP)等離子反應腔,本發明刻蝕方法也可以用於電感耦合型(ICP)等離子反應腔。與電容耦合型相比主要的區別是:ICP是通過圍繞反應腔的線圈將射頻功率穿透反應空間週邊的絕緣材料窗進入反應空間實現對反應氣體的電離。其他能夠對反應氣體電離的反應腔結構都能用於本發明的刻蝕方法,由於與本發明方法主要特徵點影響不大,所以在此不再贅述。 Figure 1 shows a plasma reaction chamber 1 which is etched in accordance with the present invention. The reaction chamber 1 includes a base 33 to which a radio frequency power source is connected. The pedestal 33 is also connected to the lower electrode as a low frequency RF power. After the plasma is ignited, the energy of the plasma is adjusted by adjusting the power of the low frequency RF power source. The base 33 includes a substrate holding device 34, which may be an electrostatic chuck or a mechanical chuck. The substrate to be processed 30 is fixed above the substrate holding device 34. The periphery of the substrate 30 also includes an edge ring 36 for controlling the temperature at the edge of the substrate, the electric field distribution, etc., and also protecting the underlying device from plasma corrosion that is ignited in the reaction chamber. The top of the reaction chamber opposite the susceptor also includes a gas diffusion device 40 coupled to a gas source 50, which may be a conventional gas shower head or other gas jet head. In addition to the capacitively coupled (CCP) plasma reaction chamber shown in Figure 1, the etching method of the present invention can also be used in an inductively coupled (ICP) plasma reaction chamber. The main difference compared with the capacitive coupling type is that the ICP ionizes the reaction gas by passing the RF power through the insulating material window around the reaction space into the reaction space around the coil of the reaction chamber. Other reaction chamber structures capable of ionizing the reaction gas can be used in the etching method of the present invention, and since they have little influence on the main feature points of the method of the present invention, they will not be described herein.

圖2顯示了本發明一個實施例的刻蝕材料層結構示意圖。其中本發明刻蝕目標層20通常是絕緣材料層,如SiO2、low-K材料等,在刻蝕目標層上分別覆蓋 有厚度較大底層光刻膠層13(BPR),中間掩膜層12如TEOS材料層,以及最上方的光刻膠層10(PR)和光刻膠緊鄰下方的防反射層11(BARC)。 2 is a schematic view showing the structure of an etched material layer according to an embodiment of the present invention. The etch target layer 20 of the present invention is usually an insulating material layer, such as SiO2, low-K material, etc., which are respectively covered on the etch target layer. There is a thicker underlayer photoresist layer 13 (BPR), an intermediate mask layer 12 such as a TEOS material layer, and an uppermost photoresist layer 10 (PR) and an anti-reflective layer 11 (BARC) immediately below the photoresist. .

在加工開始時首先通過傳統方法利用光刻技術獲得放大後的目標圖形。並形成孔洞或溝槽,在利用這一圖形刻蝕下方的防反射層11和中間掩膜層12,形成第一圖形100如圖3所示的。最後利用該中間掩膜層為掩膜將圖形100刻蝕轉換到下方的有機物材料層13中去。BPR材料層13的厚度選擇根據臨界尺寸縮小的需要來定。通常比傳統的光刻膠層要厚很多,可以達到100 nm以上,如150 nm,甚至200 nm。底層光刻膠層(BPR)雖然也叫光刻膠層但是其材料並不完全與上方的光刻膠層10相同,比如底層光刻膠層(BPR)不需要添加光敏材料。兩者都叫光刻膠僅說明所用材料類似,都是比較柔軟的有機物材料並不代表兩者相同。在利用中間掩膜層刻蝕有機物材料層13時,如圖3所示,在有機物材料層中形成梯形的剖面結構最終形成需要的臨界尺寸的圖形101。 At the beginning of the process, the enlarged target pattern is first obtained by a conventional method using a photolithography technique. Holes or trenches are formed, and the lower anti-reflection layer 11 and the intermediate mask layer 12 are etched using this pattern to form the first pattern 100 as shown in FIG. Finally, the intermediate mask layer is used as a mask to etch the pattern 100 into the underlying organic material layer 13. The thickness selection of the BPR material layer 13 is determined according to the need to narrow the critical dimension. It is usually much thicker than a conventional photoresist layer and can reach more than 100 nm, such as 150 nm or even 200 nm. The underlying photoresist layer (BPR), although also referred to as a photoresist layer, is not completely identical in material to the overlying photoresist layer 10, such as a bottom photoresist layer (BPR) that does not require the addition of a photosensitive material. Both are called photoresists, which only show that the materials used are similar. The relatively soft organic materials do not mean the same. When the organic material layer 13 is etched using the intermediate mask layer, as shown in FIG. 3, a trapezoidal cross-sectional structure is formed in the organic material layer to finally form the pattern 101 of the critical dimension required.

本發明第一實施例在利用中間掩膜層12刻蝕有機物材料層13時向反應腔內通入反應氣體。該反應氣體包括主要刻蝕氣體如O2用於被射頻電場作用解離出氧離子或氧的自由基與有機物層反應,氧化後形成氣體被抽走。為了保護側壁還要提供側壁鈍化氣體,如COS。COS能與有機物層側壁的碳原子結合形成穩固的化學鍵,防止其被主要刻蝕氣體氧化,從而防止側壁被刻蝕形成弧形結構。鈍化氣體也可以起到減緩刻蝕速率的作 用。除了鈍化氣體外還可以添加稀釋氣體如N2、Ar、CO等,通過調整稀釋氣體的量可以調節整體的刻蝕速率和氣體的濃度。通過注入上述處理氣體在反應腔內達到氣壓20 mt或者更低,施加射頻功率的大小取決於刻蝕的有機物層的厚度和上面中間掩膜層的材料。100-1000W,60 Mhz的射頻功率是一種典型應用。連接到下電極33的低頻(2/13Mhz)功率小於250W。下面以具體實施例來說明本發明的刻蝕工藝和效果。本發明第一實施例,其中通入的處理氣體包括主刻蝕氣體O2流量30 sccm,稀釋氣體CO氣體200 sccm以及側壁鈍化氣體COS流量20 sccm,達到氣壓10 mt,以600W功率的60 Mhz射頻電場施加到等離子反應腔持續30秒。其刻蝕效果如圖5所示。 In the first embodiment of the present invention, the reactant gas is introduced into the reaction chamber when the organic material layer 13 is etched by the intermediate mask layer 12. The reaction gas includes a main etching gas such as O2 for reacting a radical which is desorbed from the oxygen ion or oxygen by the radio frequency electric field to react with the organic layer, and the formed gas is removed after the oxidation. In order to protect the sidewalls, a sidewall passivation gas such as COS is also provided. The COS can combine with the carbon atoms on the sidewall of the organic layer to form a stable chemical bond, preventing it from being oxidized by the main etching gas, thereby preventing the sidewall from being etched to form an arc structure. Passivation gas can also act to slow down the etch rate use. In addition to the passivation gas, a diluent gas such as N2, Ar, CO, or the like may be added, and the overall etching rate and gas concentration can be adjusted by adjusting the amount of the dilution gas. By injecting the above-mentioned process gas into the reaction chamber to a gas pressure of 20 mt or less, the magnitude of the applied radio frequency power depends on the thickness of the etched organic layer and the material of the upper intermediate mask layer. 100-1000W, 60 Mhz RF power is a typical application. The low frequency (2/13 Mhz) power connected to the lower electrode 33 is less than 250 W. The etching process and effect of the present invention will be described below by way of specific examples. In the first embodiment of the present invention, the processing gas introduced therein includes a main etching gas O2 flow rate of 30 sccm, a dilution gas CO gas of 200 sccm, and a sidewall passivation gas COS flow rate of 20 sccm, reaching a gas pressure of 10 mt, and a 60 Mhz radio frequency of 600 W power. An electric field was applied to the plasma reaction chamber for 30 seconds. The etching effect is shown in Figure 5.

利用氧氣作為有機物層主刻蝕氣體,會很容易造成側壁被刻蝕形成等向性刻蝕的弧形側壁。所以本發明在主刻蝕氣體以外添加了大量稀釋氣體,稀釋氣體的流量遠大於主刻蝕氣體O2,達到20:3,再配合少量側壁保護氣體就能實現對有機物層的精確刻蝕,同時保證刻蝕速率。其中稀釋氣體和主刻蝕氣體比例在5:1到8:1之間甚至5:1到10:1之間仍然能實現本發明的刻蝕目的。相應的,稀釋氣體的流量與側壁保護氣體COS的流量比可以在20:1到6:1之間選擇。採用這些氣體流量比仍然能實現如圖5所示的刻蝕效果。 The use of oxygen as the main etching gas for the organic layer can easily cause the sidewalls to be etched to form an isotropically etched curved sidewall. Therefore, the present invention adds a large amount of diluent gas in addition to the main etching gas, and the flow rate of the diluent gas is much larger than the main etching gas O2, reaching 20:3, and then a small amount of the sidewall shielding gas can be used to accurately etch the organic layer. Ensure the etch rate. The etching target of the present invention can still be achieved between the ratio of the diluent gas and the main etching gas between 5:1 and 8:1 and even between 5:1 and 10:1. Correspondingly, the flow ratio of the dilution gas to the side wall shielding gas COS can be selected between 20:1 and 6:1. The etching effect as shown in Fig. 5 can still be achieved by using these gas flow ratios.

上述刻蝕所用的氣體流量氣壓和功率參數都是以電容耦合型反應腔為基礎獲得的,本發明也可以用於電壓耦合型反應腔(ICP)其參數將會有很大不同,但是 基本的發明思想相同,所用其氣體流量的比例將是與本發明上述實施例中敍述的相近。即使同樣是電容耦合型(CCP)等離子反應腔也會略有不同,同樣只要符合本發明思想的,只要氣體的用途和流量比與本發明在專利範圍中定義相同都屬於本發明內容。 The gas flow pressure and power parameters used in the above etching are obtained based on the capacitive coupling type reaction chamber, and the present invention can also be applied to a voltage coupled type reaction chamber (ICP), and the parameters thereof will be very different, but The basic inventive idea is the same, and the ratio of the gas flow rate used will be similar to that described in the above embodiment of the present invention. Even the same capacitive coupling type (CCP) plasma reaction chamber will be slightly different, and as long as it conforms to the idea of the present invention, it is within the scope of the invention as long as the gas use and flow ratio are the same as defined in the patent scope of the present invention.

本說明書實施例中所用的術語和表達方式是用來描述發明而不是限制,所以這些表達都不應排除任何等同物或者可替換物。此外,本領域技術人員通過對本發明說明書的理解和對本發明的實踐,能夠容易地想到其他實現方式。本文所描述的多個實施例中各個方面和/或部件可以被單獨採用或者組合採用。需要強調的是,說明書和實施例僅作為舉例,本發明實際的範圍和思路通過下面的專利範圍來定義。 The terms and expressions used in the description of the present specification are intended to describe the invention and not to be construed as a limitation. In addition, other implementations will be readily apparent to those skilled in the <RTIgt; Various aspects and/or components of the various embodiments described herein can be employed individually or in combination. It is to be understood that the specification and examples are by way of example only, and the scope of the invention

1‧‧‧等離子反應腔 1‧‧‧plasma reaction chamber

10‧‧‧光刻膠層 10‧‧‧Photoresist layer

11‧‧‧防反射層 11‧‧‧Anti-reflection layer

12‧‧‧中間掩膜層 12‧‧‧Intermediate mask

13‧‧‧光刻膠層 13‧‧‧Photoresist layer

20‧‧‧刻蝕目標層 20‧‧‧ etching target layer

100‧‧‧圖形 100‧‧‧ graphics

101‧‧‧圖形 101‧‧‧ graphics

30‧‧‧基片 30‧‧‧Substrate

33‧‧‧基座 33‧‧‧Base

34‧‧‧基片固定裝置 34‧‧‧Substrate fixture

36‧‧‧邊緣環 36‧‧‧Edge ring

40‧‧‧氣體擴散裝置 40‧‧‧Gas diffuser

50‧‧‧氣源 50‧‧‧ gas source

圖1顯示了本發明一個等離子反應腔圖示。 Figure 1 shows a graphical representation of a plasma reaction chamber of the present invention.

圖2顯示了根據本發明一個實施例的刻蝕材料層結構示意圖 2 is a schematic view showing the structure of an etched material layer according to an embodiment of the present invention.

圖3顯示了本發明一個實施例通過光刻形成圖形化掩膜層後的材料層結構示意圖。 FIG. 3 is a schematic view showing the structure of a material layer after forming a patterned mask layer by photolithography according to an embodiment of the present invention.

圖4顯示了本發明一個實施例的通過掩膜層刻蝕有機物材料層後的材料層刻蝕結構示意圖。 4 is a schematic view showing an etching structure of a material layer after etching an organic material layer through a mask layer according to an embodiment of the present invention.

圖5顯示了利用本發明實施例刻蝕方法刻蝕有機物材料層後材料層的截面圖。 Figure 5 is a cross-sectional view showing a material layer after etching an organic material layer by an etching method of an embodiment of the present invention.

11‧‧‧防反射層 11‧‧‧Anti-reflection layer

12‧‧‧中間掩膜層 12‧‧‧Intermediate mask

13‧‧‧光刻膠層 13‧‧‧Photoresist layer

20‧‧‧刻蝕目標層 20‧‧‧ etching target layer

100‧‧‧圖形 100‧‧‧ graphics

101‧‧‧圖形 101‧‧‧ graphics

Claims (10)

一種有機物層刻蝕方法,包括:將待刻蝕基片放入等離子反應腔,該基片上包括刻蝕目標有機物材料層;通入反應氣體到該等離子反應腔;向該反應氣體施加射頻電能點燃等離子體,對該基片進行刻蝕;其中該反應氣體包括主刻蝕氣體、稀釋氣體和側壁保護氣體,其中該主刻蝕氣體分子為O2,該稀釋氣體選自Ar、N2、CO之一或者該些氣體的混合物,該側壁保護氣體為COS,該稀釋氣體流量大於該主刻蝕氣體流量,該側壁保護氣體流量小於該主刻蝕氣體流量。 An organic layer etching method comprises: placing a substrate to be etched into a plasma reaction chamber, the substrate comprising etching a target organic material layer; introducing a reaction gas into the plasma reaction chamber; and applying radio frequency electric energy to the reaction gas to ignite The substrate is etched by the plasma; wherein the reactive gas comprises a main etching gas, a diluent gas and a sidewall shielding gas, wherein the main etching gas molecule is O2, and the diluent gas is selected from one of Ar, N2 and CO Or a mixture of the gases, the sidewall shielding gas is COS, the dilution gas flow rate is greater than the main etching gas flow rate, and the sidewall shielding gas flow rate is less than the main etching gas flow rate. 如申請專利範圍第1項所述之有機物層刻蝕方法,其中該刻蝕目標有機物材料層包括一層有機物掩膜材料層,以及位於該有機物掩膜材料層上方圖形化的無機材料層,該圖形化的無機材料層具有第一臨界尺寸。 The organic layer etching method according to claim 1, wherein the etching target organic material layer comprises a layer of an organic mask material, and a patterned inorganic material layer above the organic mask material layer, the graphic The layer of inorganic material has a first critical dimension. 如申請專利範圍第2項所述之有機物層刻蝕方法,其中該圖形化的無機材料層的圖形係通過位於其上方的具有該第一臨界尺寸圖形的光刻膠為掩膜而刻蝕獲得。 The method for etching an organic layer according to claim 2, wherein the pattern of the patterned inorganic material layer is etched by using a photoresist having the first critical dimension pattern as a mask thereon. . 如申請專利範圍第2項所述之有機物層刻蝕方法,其中該有機物掩膜材料層係通過刻蝕而在材料層底部形成具有第二臨界尺寸的圖形,其中該第二臨界尺寸小於該第一臨界尺寸。 The organic layer etching method according to claim 2, wherein the organic mask material layer forms a pattern having a second critical dimension at the bottom of the material layer by etching, wherein the second critical dimension is smaller than the first A critical dimension. 如申請專利範圍第4項所述之有機物層刻蝕方法,其中以具有該第二臨界尺寸圖形的該有機物掩膜材料層為掩膜而刻蝕下方的第二無機材料層。 The organic layer etching method according to claim 4, wherein the underlying second inorganic material layer is etched by using the organic mask material layer having the second critical dimension pattern as a mask. 如申請專利範圍第2項所述之有機物層刻蝕方法,其中該有機物掩膜材料層厚度大於100 nm。 The organic layer etching method according to claim 2, wherein the organic mask material layer has a thickness greater than 100 nm. 如申請專利範圍第1項所述之有機物層刻蝕方法,其中該反應腔中通入反應氣體中該稀釋氣體與該主刻蝕氣體O2的流量比為5:1~10:1。 The organic layer etching method according to claim 1, wherein a flow ratio of the diluent gas to the main etching gas O2 in the reaction gas into the reaction chamber is 5:1 to 10:1. 如申請專利範圍第7項所述之有機物層刻蝕方法,其中該反應腔中通入反應氣體中該稀釋氣體與該主刻蝕氣體O2的流量比為5:1~8:1。 The method for etching an organic layer according to claim 7, wherein a flow ratio of the diluent gas to the main etching gas O2 in the reaction gas into the reaction chamber is 5:1 to 8:1. 如申請專利範圍第7項所述之有機物層刻蝕方法,其中該反應腔中通入反應氣體中該稀釋氣體的流量與該側壁保護氣體COS的流量比在20:1到6:1之間。 The method for etching an organic layer according to claim 7, wherein a ratio of a flow rate of the diluent gas to the reaction gas COS in the reaction chamber is between 20:1 and 6:1. . 如申請專利範圍第1項所述之有機物層刻蝕方法,其中該射頻電能施加為100-1000W的射頻電能,刻蝕時間持續大於30秒。 The organic layer etching method according to claim 1, wherein the radio frequency electric energy is applied to 100-1000 W of radio frequency electric energy, and the etching time is longer than 30 seconds.
TW101110048A 2012-01-31 2012-03-23 Organic layer etching method TWI533354B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210022072.7A CN103227108B (en) 2012-01-31 2012-01-31 A kind of organic matter layer lithographic method

Publications (2)

Publication Number Publication Date
TW201331985A true TW201331985A (en) 2013-08-01
TWI533354B TWI533354B (en) 2016-05-11

Family

ID=48837505

Family Applications (1)

Application Number Title Priority Date Filing Date
TW101110048A TWI533354B (en) 2012-01-31 2012-03-23 Organic layer etching method

Country Status (2)

Country Link
CN (1) CN103227108B (en)
TW (1) TWI533354B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113774720B (en) * 2021-07-21 2022-07-12 杭州超探新材料科技有限公司 Carbon fiber paper and preparation method thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040041272A1 (en) * 2002-08-29 2004-03-04 Signorini Karen T. Method for etching anti-reflectant coating layers
US8124516B2 (en) * 2006-08-21 2012-02-28 Lam Research Corporation Trilayer resist organic layer etch
CN101866848B (en) * 2010-04-29 2012-05-30 中微半导体设备(上海)有限公司 Plasma etching method for etching organic matter layer
CN102208333A (en) * 2011-05-27 2011-10-05 中微半导体设备(上海)有限公司 Plasma etching method

Also Published As

Publication number Publication date
TWI533354B (en) 2016-05-11
CN103227108A (en) 2013-07-31
CN103227108B (en) 2016-01-06

Similar Documents

Publication Publication Date Title
US10157750B2 (en) Plasma processing method and plasma processing apparatus
US7361607B2 (en) Method for multi-layer resist plasma etch
TWI401741B (en) Plasma etching method
IL180025A (en) Method for bilayer resist plasma etch
CN103081074B (en) The manufacture method of substrate processing method using same, pattern formation method, semiconductor element and semiconductor element
JP2006066408A (en) Dry etching method
US11264249B2 (en) Carbon containing hardmask removal process using sulfur containing process gas
KR101070568B1 (en) Method for forming silicon oxide film, plasma processing apparatus and storage medium
TWI552221B (en) Method for providing high etch rate
TWI795625B (en) Plasma treatment method
TWI533354B (en) Organic layer etching method
TW201332018A (en) Etching method for organic substance layer
TWI650814B (en) Plasma etching method
US20030153193A1 (en) Etching method
US11881410B2 (en) Substrate processing apparatus and plasma processing apparatus
TWI442469B (en) A plasma etching method for carbon - containing layer
TW202335067A (en) Bias voltage modulation approach for sio/sin layer alternating etch process