TWI228282B - A method for fabricating disposable spacer - Google Patents
A method for fabricating disposable spacer Download PDFInfo
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- TWI228282B TWI228282B TW92131592A TW92131592A TWI228282B TW I228282 B TWI228282 B TW I228282B TW 92131592 A TW92131592 A TW 92131592A TW 92131592 A TW92131592 A TW 92131592A TW I228282 B TWI228282 B TW I228282B
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- disposable
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- partition wall
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- 125000006850 spacer group Chemical group 0.000 title claims abstract description 43
- 238000000034 method Methods 0.000 title claims abstract description 40
- 229920000642 polymer Polymers 0.000 claims abstract description 26
- 238000011065 in-situ storage Methods 0.000 claims abstract 2
- 239000000463 material Substances 0.000 claims description 59
- 238000004519 manufacturing process Methods 0.000 claims description 55
- 238000005192 partition Methods 0.000 claims description 54
- 238000005530 etching Methods 0.000 claims description 41
- 239000000126 substance Substances 0.000 claims description 32
- 239000000758 substrate Substances 0.000 claims description 28
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 26
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 15
- 239000000460 chlorine Substances 0.000 claims description 14
- 229910052801 chlorine Inorganic materials 0.000 claims description 14
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 13
- 229910052786 argon Inorganic materials 0.000 claims description 13
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 13
- 229910052794 bromium Inorganic materials 0.000 claims description 13
- 239000001307 helium Substances 0.000 claims description 13
- 229910052734 helium Inorganic materials 0.000 claims description 13
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 13
- 239000000376 reactant Substances 0.000 claims description 12
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 10
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 10
- 239000000654 additive Substances 0.000 claims description 9
- 230000004888 barrier function Effects 0.000 claims description 9
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims description 9
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 230000000996 additive effect Effects 0.000 claims description 8
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims description 8
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 7
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 6
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 claims description 6
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 3
- 239000007789 gas Substances 0.000 claims description 3
- 229910000042 hydrogen bromide Inorganic materials 0.000 claims description 3
- 229920000620 organic polymer Polymers 0.000 claims description 3
- -1 monooxy Chemical group 0.000 claims description 2
- 241000238631 Hexapoda Species 0.000 claims 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims 1
- 239000011733 molybdenum Substances 0.000 claims 1
- 229910052750 molybdenum Inorganic materials 0.000 claims 1
- 238000002513 implantation Methods 0.000 abstract 1
- 230000008569 process Effects 0.000 description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 238000000151 deposition Methods 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000004575 stone Substances 0.000 description 6
- 238000005468 ion implantation Methods 0.000 description 5
- 238000005229 chemical vapour deposition Methods 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- 241001674048 Phthiraptera Species 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000001459 lithography Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 241000208340 Araliaceae Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000002322 conducting polymer Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
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- Drying Of Semiconductors (AREA)
Abstract
Description
12282821228282
五、發明說明(1) 【發明所屬之技術領域 本發明是有關於一種可物|本jV. Description of the invention (1) [Technical field to which the invention belongs The present invention relates to a kind of material | 本 j
Spacer), , Λ (Iη-si tu)方式進行高合;取人 匆 ^ ^ ^ ^ ea ^ 子♦合物間隙壁之沉積盥蝕釗认 可拋棄式間隙壁製造方法。 谓”蚀刻的 【先前技術】 叫參…、第1圖至第4圖,第i圖至第4 、 間隙壁之製程剖面圖。首先,提供由石夕(Si : =Spacer),, Λ (Iη-si tu) method to carry out high-coupling; take a hurry ^ ^ ^ ^ ea ^ ♦ The deposition of composite spacers can be considered a manufacturing method of disposable spacers. The "prior art" of "etching" is called ginseng ..., Fig. 1 to Fig. 4, Fig. I to Fig. 4, and sectional views of the manufacturing process of the partition wall. First, provide by Xi Xi (Si: =
100,再利用熱氧化的方式於基材100上形成氧化石夕基相 (Silicon Oxide)薄膜做為閘極介電層1〇2。完成閘極介 層102之成長後,利用沉積方式形成複晶矽(p〇iysiiic〇n〕 薄膜(未^會示)覆蓋在閘極介電層1〇2上。再利用微影與蝕/ 刻方式定義此複晶矽薄膜,而移除部分之複晶矽薄膜並暴 露出部分之閘極介電層102,藉以在閘極介電層1〇2上形成 閘極1 0 4,如第1圖所示。100, and then a thermal oxidation method is used to form a Silicon Oxide thin film on the substrate 100 as the gate dielectric layer 102. After the growth of the gate dielectric layer 102 is completed, a polycrystalline silicon (p〇iysiiicOn) thin film (not shown) is formed by a deposition method to cover the gate dielectric layer 102. Reusing lithography and etching / The polycrystalline silicon film is defined in a engraved manner, and a part of the polycrystalline silicon film is removed and a part of the gate dielectric layer 102 is exposed, so as to form a gate 104 on the gate dielectric layer 102, as in 1 picture.
接著’利用化學氣相沉積(Chemical Vap〇r Depositi〇n ; CVD)方式或熱爐管(Furnace)方式,於化學氣相沉積反應 室或爐管内’形成間隙壁材料層1〇6覆蓋在閘極1〇4以及暴 露之閘極介電層1〇2上。其中,間隙壁材料層1〇6之材質一 般係採用氮化石夕(Silicon Nitride)以及氧化石夕,如第2圖 所示。 待完成間隙壁材料層1 〇6之沉積後,將基材1 〇〇連同其上之 結構移至蝕刻機台之蝕刻室,並對間隙壁材料層丨〇 6進行Next, a 'chemical vapor deposition (CVD) method or a thermal furnace method (Furnace method) is used to form a spacer material layer 106 in the chemical vapor deposition reaction chamber or furnace tube to cover the gate. Electrode 104 and exposed gate dielectric layer 102. Among them, the material of the spacer material layer 106 is generally made of silicon nitride oxide (Silicon Nitride) and oxide silicon oxide, as shown in FIG. 2. After the deposition of the spacer material layer 106 is completed, the substrate 100 with the structure thereon is moved to the etching chamber of the etching machine, and the spacer material layer
第5頁 1228282 五、發明說明(2) ___ 蝕刻步驟,直至暴露出閘極104為止, 上形成間隙壁108。完成間隙壁1〇8之在閘極丨〇4之侧壁 彳離子植人技術分別•基材i Q "形J :二厂 114、以及没極112,而形成如第3 :1 二與掺雜區 由於,完成源極110與推雜區114、以之^ ° 入步驟後’㈣壁已完成其階段性之^112之離子植 蝕刻的方式將剩餘之間隙壁丨〇8予以 犯,而可利用 如第4圖所示。因此,間隙壁1〇8又稱為除’所形成之結構 然而,氮化石夕或氧化石夕所構成之壁厂,隙壁。 易。由於,氮化石夕或氧化石夕所構成J = = 2容 步驟後,間隙壁之表面會形成一層硬化声j在離子植入 Layer)。受到間隙壁表面之硬化層的影纟 , :KWet Etching)的方式順利移除間隙壁曰 以用:式蝕 式蝕刻(Dry Etching)的方式來移 卜,運用乾 成之間隙壁時,此乾式飯刻步驟所使^^或,化石夕所構 物,會傷害到底下之閘極介電 =鼠(F)化學 層以及基材之品質。另一;:層=材’而影響間極介電 須分學氣相沉積反應室或爐管壁 長了裏転時間,更增加製程的複雜度。 【發明内容】 因此’本發明之目的銶县 造方法’其係以含碳氫ι化一種棄式間隙壁之製 基化學物為原料,於閘極二物以及一虱氣(Cl2)與溴(Br) "閘極之側壁上形成高分子聚合物層來 第6頁 I228282Page 5 1228282 V. Description of the invention (2) ___ An etching step is performed until the gate electrode 104 is exposed, and a spacer wall 108 is formed thereon. Complete the side wall of the spacer 1 08 on the side of the gate 丨 04 彳 ion implantation technology respectively • substrate i Q " shape J: the second plant 114, and the immortal 112, and formed as the third 3: 1 two and In the doped region, the remaining spacers are committed by way of the ion implantation method after the source electrode 110 and the dopant region 114 are completed, and the steps are completed. It can be used as shown in Figure 4. Therefore, the partition wall 108 is also referred to as the structure formed by the addition of '. However, the wall plant composed of nitrided stone or oxidized stone is called the partition wall. easy. Because the nitride stone or the oxide stone is composed of J = = 2 volume steps, a hardened sound will be formed on the surface of the gap wall (in the ion implantation layer). Under the influence of the hardened layer on the surface of the gap wall,: KWet Etching) successfully removes the gap wall by using: Dry Etching. When using the dry gap wall, this dry type ^^ or the structure of the fossil evening will damage the gate dielectric = rat (F) chemical layer and the quality of the substrate. Another :: layer = material 'affects the inter-electrode dielectric. The vapor deposition reaction chamber or furnace tube wall has to be studied separately, which has prolonged the cycle time and increased the complexity of the process. [Summary of the Invention] Therefore, 'the objective of the present invention is to make a method from Shexian County', which is based on the production of a base-based chemical containing a type of discarded bulkhead containing hydrocarbons, the second electrode and a lice gas (Cl2) and bromine. (Br) " Polymer layer is formed on the side wall of the gate electrode Page 6 I228282
五、發明說明(3) ,為可搬棄式間隙壁之材料。由於高分子 =2削所移除,因此可在降低對基材與間極\了電%易的為 >害下,順利移除此可拋棄式間隙壁。 ^曰的 法:^臨二::在提供一種可拋棄式間隙壁之製造方 、係以^ %方式,而在同一蝕刻機中進行高分子 :隙壁之沉積與蝕刻。由於不須轉換反應室; „而可降低製程成本支出,並可提升製:間 ^發明之又一目的是在提供一種可拋棄式間隙壁之= 法,其係在蝕刻機中進行高分子聚合物間隙壁材料之沉 積,藉由調整蝕刻機之偏壓電力(Bias p〇wer),可改盖言 刀子聚合物之階梯覆蓋(Step c〇verage)能力。 根據本發明之上述目的,提出一種可拋棄式間隙壁之製造 方法,至少包括下列步驟··首先,提供一基材,其中此基 材上至少已形成一閘極。接著,利用一反應物形成一間隙 壁材料層覆蓋在上述之閘極以及基材上,其中此反應物至 $包括一含碳氫氟化學物。其中,此反應物更至少包括氯 氣(C丨2)或溴(B r)基化學物。然後,以一臨場方式對上述之 間隙壁材料層進行一蝕刻步驟,而在閘極之側壁形成可拋 棄式間隙壁。 依照本發明一較佳實施例,形成間隙壁材料層之步驟與蝕 刻步驟均在同一蝕刻室中進行。此外,上述之含碳氫氣化 學物可為四氟化碳(CL)、三氟曱烷(CHf3)、二氟甲烷(Ch2 h)、或氟甲烷(C^F),且含碳氫氟化學物之流量較佳是& 於lOsccm至200sccm之間。此外,上述之氯氣或溴基化學V. Description of the invention (3), which is the material of the removable partition wall. Because the polymer = 2 is removed, the disposable wall can be removed smoothly without reducing the damage to the substrate and the electrode. ^ Said method: ^ Pro 2 :: In providing a manufacturing method of disposable wall spacers, the polymer and the wall spacers are deposited and etched in the same etching machine in a ^% manner. Because it is not necessary to switch the reaction chamber; „It can reduce the process cost and increase the production cost: Another purpose of the invention is to provide a disposable barrier wall method, which is a polymer polymerization in an etching machine The deposition of the material of the spacer wall can be changed to cover the step polymer capability of the knife polymer by adjusting the bias power of the etching machine (Bias power). According to the above object of the present invention, a kind of The manufacturing method of the disposable spacer comprises at least the following steps. First, a substrate is provided, wherein at least a gate electrode has been formed on the substrate. Then, a reactant is used to form a spacer material layer to cover the above. The gate electrode and the substrate, wherein the reactant includes a hydrocarbon-containing chemical. The reactant further includes at least a chlorine (C2) or bromine (Br) -based chemical. Then, a An etching step is performed on the above-mentioned spacer material layer on the spot, and a disposable spacer is formed on the side wall of the gate electrode. According to a preferred embodiment of the present invention, the step of forming the spacer material layer and the etching step All are performed in the same etching chamber. In addition, the above-mentioned carbon-containing hydrogen chemical may be carbon tetrafluoride (CL), trifluoromethane (CHf3), difluoromethane (Ch2 h), or fluoromethane (C ^ F ), And the flow rate of the hydrocarbon-containing chemical is preferably & between lOsccm to 200sccm. In addition, the above-mentioned chlorine or bromine-based chemistry
1228282 五、發明說明(4) 物之流量較佳是控制在介於lOsccm至20 0sccm之間,更佳 則係控制在介於3 0 s c c m至5 0 s c c m之間。而形成間隙壁材料 層之步驟至少包括控制反應室之偏壓電力(Bias Power)小 於2 0瓦(W)。另外,進行蝕刻步驟時,至少包括:使用一 氧基(02 Base)化學物;使用添加物,其中此添加物較佳可 為氬(Ar)或氦(He),或者氯或溴化氫;以及較佳是將反應 室之偏壓電力控制在介於10瓦至20 0瓦之間。其中,氧基 化學物亦可以聯銨(Nd2)或臭氧(03)取代。此外,氬或氦之 流量較佳是控制在介於5 0 s c c m至5 0 0 s c c m,更佳是控制在 介於80seem至120sccm之間。在本發明之一較佳實施例 中’間隙壁材料層之厚度較佳是介於1〇〇A至1〇〇叹之間。 由於’氧電漿可輕易移除由高分子聚合物所構成之間隙 壁’再加上形成間隙壁材料層之步驟以及間隙壁材料層之 钮刻步驟均在同一蝕刻室中進行。因此,不僅可在降低對 基材之損傷的情況下,有效移除此一可拋棄式間隙壁;更 I簡化製程,而可降低製程成本,進而可達到提升製程 W. rtf" AAfc Q 上 JL ^ 【實施方式】 本發明揭露一種可拋棄式間隙壁之製造方法,其 =式,進行高分子聚合物的沉積與蝕刻以製作可拋 每 以及提升製程可錢,更可輕易;=可==程成本、 而降低對基材與間隙壁之損傷 了、:土棄式間隙壁, 馮了使本發明之敘述更加1228282 V. Description of the invention (4) The flow rate of the substance is preferably controlled between lOsccm and 20sccm, more preferably it is controlled between 30sccm and 50sccm. The step of forming the spacer material layer includes controlling at least Bias Power of the reaction chamber to be less than 20 watts (W). In addition, when performing the etching step, at least: using a monooxy (02 Base) chemical; using an additive, wherein the additive is preferably argon (Ar) or helium (He), or chlorine or hydrogen bromide; And preferably, the bias power of the reaction chamber is controlled between 10 watts and 200 watts. Among them, oxychemicals can also be substituted with ammonium (Nd2) or ozone (03). In addition, the flow rate of argon or helium is preferably controlled between 50 s c c m and 50 0 s c c m, and more preferably between 80 seec and 120 sccm. In a preferred embodiment of the present invention, the thickness of the 'partition wall material layer' is preferably between 100 A and 100 Å. Because the "oxygen plasma can easily remove the spacer formed by the polymer", plus the step of forming the spacer material layer and the step of embossing the spacer material layer are performed in the same etching chamber. Therefore, not only can the disposable spacer be effectively removed under the condition of reducing the damage to the substrate; it also simplifies the manufacturing process, but can reduce the manufacturing cost, and then can improve the manufacturing process. W. rtf " AAfc Q on JL ^ [Embodiment] The present invention discloses a method for manufacturing a disposable partition wall. The method is to perform deposition and etching of high-molecular polymers to make disposable products and improve the manufacturing process. It is easier; = 可 == Process cost, and reduce the damage to the substrate and the partition wall: soil-discarded partition wall, which makes the description of the present invention more
1228282 五、發明說明(5) J盡與完備’可參照下列描述並配合第5圖至第8圖之圖 圖/第8圖,第5圖至第8圖係•示依照本發明-較佳貫訑例的一種可拋棄式間隙壁之製程剖面圖。首 -提供半導體之基材200,其中此基材2〇〇之 為 石:。再:用例如熱氧化或化學氣相沉積的方式,么J薄 的閘^電層覆蓋在基材_上,其中閘極介電層2〇2 之材質可例如為氧化石夕。閘極介電層202形成後, ,如化學氣相沉積的方式形成導電材料薄膜(未繪示)覆蓋 ΐ閑上,㊣中此導電材料薄膜較佳可為複晶 材料薄媒進行定義,以去二;:===;: 部分之閘極介電層202,而在閘極 〇上;成出 _,如所示。 策摩202上形成閘極 閘極204形成後,將基材2〇〇連同其上之結構置入 中’再利用沉積的方式形成間隙壁材料層2 204以及閘極介電層202上,如第6圖所示。其中,孝 姓刻室可例如為電漿鞋刻室,且所形成之間隙壁材料層 206的材質較佳為南分子聚合物’例如有機高分子聚合 物’而間隙壁材料層2〇6之厚度較佳是控制在介於魏至 1 000Α之間。在形成間隙壁材料層2〇6時,至少包括使 應物’ J中此反應物至少包括含碳氫I化學物 虱氣化學,較佳可為四氟化碳、三氟甲烧、二氟甲烧、: 及氣甲烧等。此外’形成間隙壁材乂 1228282 五、發明說明(6) 物更至少包括氯氣或溴基化學物。於形成間隙壁材料層 2 0 6期間,較佳是將含碳氫氟化學物之流量控制介於 lOsccm至20 0sccm之間,而氯氣或溴基化學物之流量較佳 是控制在介於lOsccm至200sccm之間,氯氣或漠基化學物 之流量更佳是控制在介於30sccm至50sccm之間,且較佳是 將蝕刻室之偏壓電力控制在小於2 〇瓦,以提高間隙壁材料 層206之階梯覆蓋能力’進而避免突懸(〇verhang)現象的 產生。 接著,以臨場方式,在同一蝕刻室中對間隙壁材料層2 〇 6 進行蝕刻步驟,直至暴露出閘極2〇4為止,而在閘極2〇4之 側壁上形成間隙壁208,如第7圖所示。其中,此蝕刻步驟 可為非等向性蝕刻(Anisotropic Etching)步驟。進行間 隙壁材料層206之蝕刻步驟時,可使用例如氧基化學物當 作反應物以形成氧電漿,且較佳是將蝕刻室之偏壓電力控 制在"於1 0瓦至2 〇 〇亢之間,藉以有效控制間隙壁2 〇 8之形 狀。其中,上述之氧基化學物可以聯銨或臭氧取代。另 夕卜:在:刻步驟進行期Fa,’可加入例如氬或氦,或者氯或 添加物’以㈣刻之進行。纟中,於㈣步驟進 二/間,氬或氦之流量較佳是控制在介於5〇sccm至 太恭C^m之間,更佳疋控制在介於80sccm至120sccm之間。 間4 @ ΐ欲為利用臨場方式,而在同一蝕刻室中進行 ^此可11二206之沉積與蝕刻。由於無須轉換反應室, 度縮短製程時間、與降低製程成本,進而1228282 V. Description of the invention (5) J is complete and complete. 'You can refer to the following description and cooperate with Figures 5 to 8 / Figure 8, Figures 5 to 8 are shown in accordance with the present invention-preferably A cross-sectional view of the process of a disposable bulkhead through the example. First-a semiconductor substrate 200 is provided, in which the substrate 200 is stone. Furthermore, the thin gate electrode layer is covered on the substrate by means of, for example, thermal oxidation or chemical vapor deposition, and the material of the gate dielectric layer 202 may be, for example, oxidized stone. After the gate dielectric layer 202 is formed, a conductive material film (not shown) is formed to cover the substrate, such as by chemical vapor deposition. The conductive material film may be defined as a thin film of a polycrystalline material. Go to two ;: === ;: part of the gate dielectric layer 202, and on the gate 0; into _, as shown. After the gate electrode 204 is formed on the strategy 202, the substrate 200 is placed together with the structure thereon, and then the barrier material layer 2 204 and the gate dielectric layer 202 are formed by using a deposition method, such as Figure 6 shows. Among them, the engraving room of the surname Xiao may be, for example, a plasma shoe engraving room, and the material of the spacer material layer 206 formed is preferably a South molecular polymer such as an organic polymer and the spacer material layer 206 The thickness is preferably controlled between Wei and 1 000A. When forming the spacer material layer 206, at least the reactant 'J is included. The reactant includes at least the hydrocarbon-containing chemical lice gas chemistry, preferably carbon tetrafluoride, trifluoromethane, difluoride. Kakiyaki: Kakiyaki and Kakiyaki. In addition, 'formation wall material' 1228282 V. Description of the invention (6) The substance further includes at least chlorine or bromine-based chemicals. During the formation of the spacer material layer 206, it is preferable to control the flow rate of the hydrofluorocarbon-containing chemical between lOsccm and 20sccm, and the flow rate of the chlorine or bromine-based chemical is preferably controlled between lOsccm Between 200 sccm, the flow rate of chlorine or desert-based chemicals is better controlled between 30 sccm and 50 sccm, and the bias power of the etching chamber is preferably controlled to less than 20 watts to improve the barrier material layer. The step coverage ability of 206 'further avoids the occurrence of overhang. Next, in a field manner, the spacer material layer 206 is etched in the same etching chamber until the gate electrode 204 is exposed, and a spacer wall 208 is formed on the side wall of the gate electrode 204, as described in the first section. Figure 7 shows. The etching step may be an anisotropic etching (Anisotropic Etching) step. When performing the etching step of the spacer material layer 206, for example, an oxygen chemical can be used as a reactant to form an oxygen plasma, and it is preferable to control the bias power of the etching chamber to within 10 watts to 2 watts. In between, the shape of the partition wall 208 can be effectively controlled. Among them, the above-mentioned oxychemicals may be substituted by hydrazine or ozone. In addition, during the engraving step, Fa, 'may be performed by adding, for example, argon or helium, or chlorine or additives'. In the process, in the second step, the flow rate of argon or helium is preferably controlled between 50 sccm and Tai Cong m, and more preferably controlled between 80 sccm and 120 sccm. Room 4 @ ΐΐ To make use of the on-site method, it can be performed in the same etching room. ^ This can be deposited and etched in 11206 Because there is no need to change the reaction chamber, the process time is shortened, and the process cost is reduced.
12282821228282
五、發明說明(7) ΠΓ=ΐ二Γ用例如微影《及離子植入技術 212 極210與摻雜區2“、以及沒極 。形成源極210與摻雜區214、 隙壁208已完成其階段性之任務,,及極212後,此時間 移除剩餘之間隙壁208,而形成如第^ '用?的方式 剩餘之間隙壁208時,較佳是刺爾彳,圖所不之、'構。移除 學物。由於間隙壁208係由J:! ;氧電聚當作钮刻化 氧電裝當作餘刻化學物由可γ避子免H物所構成’因此以 及基材2。。的情況下,順Λ在:剩^ =直主要:'用以辅助源極21。、^^ 隙壁208卽入進仃’當此一離子植入步驟完成後,間 J壁即可去除。因此’間隙壁m又稱為可拋棄式間: 化風:祖:斂為利用含碳氫氟化學物以及氯氣與溴式 料因此ϊ ί : ?高分子聚合物做為間隙壁2°8之材土 降低ff i用虱電漿順利移除剩餘之間隙壁208,而 閘極介電層202以及基材2◦◦之傷害,進而提升元而件 實施例可知,本發明之-優點就是因為 3料。因此,可利用氧電漿輕易移除高分子 =之 可降低對基材與閘極介電層的損害。 σ :是 由上述本發明較佳實施例可知’本發明之另一優點就是因V. Description of the invention (7) ΠΓ = ΐ 二 Γ For example, lithography, and ion implantation technology 212 electrode 210 and doped region 2 ", and non-electrode. Source 210 and doped region 214, and gap 208 have been formed. After completing its phased tasks, and after the pole 212, at this time, the remaining gap wall 208 is removed, and the remaining gap wall 208 is formed in the manner as described in the "?" Method, preferably a thorn, as shown in the figure. The structure is removed. Since the partition wall 208 is composed of J:!; Oxygen electropolymerization is used as a button to etch oxygen electrical equipment as the remaining chemical substance is composed of γ avoidance and H free matter. In the case of substrate 2., 顺 Λ :: ^ = Straight Main: 'Used to assist the source electrode 21, ^^ The gap wall 208 is inserted into 仃' When this ion implantation step is completed, the time J The wall can be removed. Therefore, the 'gap wall m' is also known as a disposable type: wind: ancestor: converged to use hydrocarbon-containing fluorochemicals and chlorine and bromine materials, so ::? High-molecular polymer as the gap The material of the wall 2 ° 8 is reduced, and the remaining gap wall 208 is smoothly removed with the lice plasma, and the damage of the gate dielectric layer 202 and the substrate 2◦ is further improved. The advantage of the present invention is because of the three materials. Therefore, the polymer can be easily removed by using an oxygen plasma = it can reduce the damage to the substrate and the gate dielectric layer. Σ: is the preferred embodiment of the present invention described above. It can be seen that another advantage of the present invention is that
第11頁 1228282 五、發明說明(8) 為係以臨場方式,在同 壁之沉積與蝕刻,而無 程、降低製程成本、以 製程可靠度的目的。 由上述本發明較佳實施 為在蝕刻機中進行高分 此’藉由調整蝕刻機之 物之階梯覆蓋能力的目 雖然本發明已以一較佳 定本發明,任何熟習此 範圍内,當可作各種之 圍當視後附之申請專利 一蝕刻機中進行高分子聚合物間隙 須轉換反應室。因此,可簡化製 及縮短製程時間,進而可達到提升 例可知’本發明之v Θ <又一優點就是因 子聚合物間隙壁分立 他^ A 璧材枓之沉積。因 偏壓電力,可洁 的。 Γ達到改善高分子聚合 實施例揭露如卜 姑_ 上,然其並非用以限 不脫離本發明之精神和 ^ 因此本發明之保護範 犯圍所界定者為準。Page 11 1228282 V. Description of the invention (8) The purpose is to deposit and etch on the same wall in the same way, without process, reducing process cost, and for process reliability. From the above, the present invention is preferably implemented to achieve a high score in the etching machine. By adjusting the step coverage capability of the etching machine, although the invention has been set with a better definition of the invention, anyone familiar with this range can be used as A variety of enclosures should be attached to the attached patent application-an etching machine for conducting polymer gaps to switch reaction chambers. Therefore, the production process can be simplified and the process time can be shortened, and further improvement can be achieved. It can be seen that ‘v Θ < another advantage of the present invention is due to the separation of the polymer polymer wall and other materials. Can be cleaned due to bias power. Γ achieves improved polymer polymerization. The embodiment is disclosed as above, but it is not intended to limit the scope of the invention without departing from the spirit and scope of the present invention.
第12頁 1228282 圖式簡單說明 【圖式簡單說明】 第1圖至第4圖係繪示習知可拋棄式間隙壁之製程剖面圖。 第5圖至第8圖係繪示依照本發明一較佳實施例的一種可拋 棄式間隙壁之製程剖面圖。 【元件代表符號簡單說明】 100 =基材 102 104 :閘極 106 108 :間隙壁 110 112 :汲極 114 200 :基材 202 204 :閘極 206Page 12 1228282 Brief description of the drawings [Simplified description of the drawings] Figures 1 to 4 are cross-sectional views showing the process of the conventional disposable wall. 5 to 8 are cross-sectional views showing a process of a disposable partition wall according to a preferred embodiment of the present invention. [Simple description of component representative symbols] 100 = substrate 102 104: gate 106 108: spacer 110 112: drain 114 200: substrate 202 204: gate 206
閘極介電層 間隙壁材料層 源極 摻雜區 閘極介電層 間隙壁材料層 208 :間隙壁 2 1 2 ·•汲極 2 1 0 :源極 2 1 4 :摻雜區Gate dielectric layer gap wall material layer source doped region gate dielectric layer gap wall material layer 208: gap wall 2 1 2 • • drain 2 1 0: source 2 1 4: doped region
第13頁Page 13
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| TW92131592A TWI228282B (en) | 2003-11-11 | 2003-11-11 | A method for fabricating disposable spacer |
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| TW92131592A TWI228282B (en) | 2003-11-11 | 2003-11-11 | A method for fabricating disposable spacer |
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| TWI228282B true TWI228282B (en) | 2005-02-21 |
| TW200516668A TW200516668A (en) | 2005-05-16 |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8324038B2 (en) | 2006-09-12 | 2012-12-04 | United Microelectronics Corp. | Method of removing a spacer, method of manufacturing a metal-oxide-semiconductor transistor device, and metal-oxide-semiconductor transistor device |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8324038B2 (en) | 2006-09-12 | 2012-12-04 | United Microelectronics Corp. | Method of removing a spacer, method of manufacturing a metal-oxide-semiconductor transistor device, and metal-oxide-semiconductor transistor device |
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