CN115373072A - C-axis preferred orientation zinc-magnesium oxide ridge waveguide and manufacturing method thereof - Google Patents
C-axis preferred orientation zinc-magnesium oxide ridge waveguide and manufacturing method thereof Download PDFInfo
- Publication number
- CN115373072A CN115373072A CN202110562784.7A CN202110562784A CN115373072A CN 115373072 A CN115373072 A CN 115373072A CN 202110562784 A CN202110562784 A CN 202110562784A CN 115373072 A CN115373072 A CN 115373072A
- Authority
- CN
- China
- Prior art keywords
- etching
- film
- axis
- masking layer
- preferred orientation
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 19
- PNHVEGMHOXTHMW-UHFFFAOYSA-N magnesium;zinc;oxygen(2-) Chemical compound [O-2].[O-2].[Mg+2].[Zn+2] PNHVEGMHOXTHMW-UHFFFAOYSA-N 0.000 title abstract 2
- 238000005530 etching Methods 0.000 claims abstract description 75
- 230000000873 masking effect Effects 0.000 claims abstract description 44
- 238000000034 method Methods 0.000 claims abstract description 44
- 238000005516 engineering process Methods 0.000 claims abstract description 25
- 238000001312 dry etching Methods 0.000 claims abstract description 14
- 239000010408 film Substances 0.000 claims description 66
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 34
- 238000010884 ion-beam technique Methods 0.000 claims description 28
- 239000010409 thin film Substances 0.000 claims description 24
- 229920002120 photoresistant polymer Polymers 0.000 claims description 23
- 238000001020 plasma etching Methods 0.000 claims description 12
- 239000000758 substrate Substances 0.000 claims description 8
- 238000009616 inductively coupled plasma Methods 0.000 claims description 6
- 238000001755 magnetron sputter deposition Methods 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 238000005234 chemical deposition Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 238000004528 spin coating Methods 0.000 claims description 3
- 238000000151 deposition Methods 0.000 claims description 2
- 229910021642 ultra pure water Inorganic materials 0.000 claims description 2
- 239000012498 ultrapure water Substances 0.000 claims description 2
- 238000001259 photo etching Methods 0.000 claims 2
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 230000003287 optical effect Effects 0.000 abstract description 8
- 239000011777 magnesium Substances 0.000 abstract 3
- 239000011701 zinc Substances 0.000 abstract 3
- 239000010410 layer Substances 0.000 description 55
- 239000007789 gas Substances 0.000 description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 16
- 229910052760 oxygen Inorganic materials 0.000 description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 10
- 239000001301 oxygen Substances 0.000 description 10
- 238000000206 photolithography Methods 0.000 description 10
- 229910052681 coesite Inorganic materials 0.000 description 8
- 229910052906 cristobalite Inorganic materials 0.000 description 8
- 239000000377 silicon dioxide Substances 0.000 description 8
- 235000012239 silicon dioxide Nutrition 0.000 description 8
- 229910052682 stishovite Inorganic materials 0.000 description 8
- 229910052905 tridymite Inorganic materials 0.000 description 8
- 238000004140 cleaning Methods 0.000 description 6
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 6
- 238000001878 scanning electron micrograph Methods 0.000 description 6
- 239000003292 glue Substances 0.000 description 5
- 238000004381 surface treatment Methods 0.000 description 5
- 230000000737 periodic effect Effects 0.000 description 4
- 238000010025 steaming Methods 0.000 description 4
- 238000000233 ultraviolet lithography Methods 0.000 description 4
- 230000009286 beneficial effect Effects 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000001039 wet etching Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000005693 optoelectronics Effects 0.000 description 2
- 229910013641 LiNbO 3 Inorganic materials 0.000 description 1
- 229910003902 SiCl 4 Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000012792 core layer Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000004549 pulsed laser deposition Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000000927 vapour-phase epitaxy Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
- G02B6/10—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type
- G02B6/12—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type of the integrated circuit kind
- G02B6/13—Integrated optical circuits characterised by the manufacturing method
- G02B6/136—Integrated optical circuits characterised by the manufacturing method by etching
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
- G02B6/10—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type
- G02B6/12—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type of the integrated circuit kind
- G02B6/122—Basic optical elements, e.g. light-guiding paths
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
- G02B6/10—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type
- G02B6/12—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type of the integrated circuit kind
- G02B2006/12035—Materials
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Optical Integrated Circuits (AREA)
Abstract
Description
技术领域technical field
本发明涉及光电子领域,尤其涉及一种c轴择优取向Zn1-xMgxO(0≤x≤0.3)脊型波导及其制作方法。The invention relates to the field of optoelectronics, in particular to a c-axis preferred orientation Zn 1-x Mg x O (0≤x≤0.3) ridge waveguide and a manufacturing method thereof.
背景技术Background technique
Zn1-xMgxO薄膜具有无毒、低原料成本、可调谐能带结构等特点,在透明导电薄膜、薄膜晶体管电子输运层、紫外发光二极管n型层和紫外光探测器n型层等方面有着重要的应用。最近的研究结果表明:c轴择优取向Zn0.72Mg0.28O薄膜具有与LiNbO3相当的二阶非线性极化率,揭示其在非线性波导和电光调制器等集成光学领域具有巨大的应用潜力。Zn 1-x Mg x O thin film has the characteristics of non-toxicity, low raw material cost, and tunable energy band structure. etc. have important applications. Recent research results show that c-axis preferentially oriented Zn 0.72 Mg 0.28 O thin films have second-order nonlinear susceptibility comparable to LiNbO 3 , revealing their great application potential in the field of integrated optics such as nonlinear waveguides and electro-optic modulators.
脊形波导对传输光在两个方向上同时进行限制,是光波耦合器、波导调制器、波导开关以及波导激光器等无源和有源器件的基础。为了在集成光学领域获得有效应用,将Zn1-xMgxO薄膜刻蚀成具有微米量级横向宽度的脊形波导结构是亟需解决的关键技术。目前已报道的仅涉及针对a轴择优取向的Zn1-xMgxO薄膜的刻蚀方法,总体包括干法和湿法两种:The ridge waveguide confines the transmitted light in two directions simultaneously, and is the basis of passive and active devices such as optical couplers, waveguide modulators, waveguide switches, and waveguide lasers. In order to obtain effective applications in the field of integrated optics, etching Zn 1-x Mg x O thin films into ridge-shaped waveguide structures with micron-scale lateral widths is a key technology that needs to be solved urgently. The currently reported etching methods only involve Zn 1-x Mg x O thin films with a-axis preferred orientation, generally including dry method and wet method:
(一)干法刻蚀(1) Dry etching
干法刻蚀的优势是非常好地控制侧壁剖面和好的片内、片间及批次间的刻蚀均匀性,但是其缺点是等离子体带来对薄膜表面的损伤。例如,美国罗格斯大学J.Zhu等人采用基于SiCl4气体的反应离子刻蚀(RIE)技术刻蚀金属有机气相外延法生长的a轴取向Zn1- xMgxO(0≤x≤0.3)薄膜。The advantage of dry etching is very good control of the sidewall profile and good etching uniformity within the chip, between chips and between batches, but its disadvantage is that the plasma causes damage to the film surface. For example, J.Zhu et al. of Rutgers University in the United States used reactive ion etching (RIE) technology based on SiCl 4 gas to etch a-axis orientation Zn 1- x Mg x O (0≤x≤ 0.3) Film.
再如,美国Lumenz公司J.Tresback等人采用基于BCl3和Cl2混合气体的电感耦合等离子体增强反应离子刻蚀(ICP-RIE)技术刻蚀金属有机气相外延法生长的a轴取向Zn1- xMgxO(0≤x≤0.3)薄膜。For another example, J. Tresback et al. from Lumenz Company of the United States used inductively coupled plasma-enhanced reactive ion etching (ICP-RIE) technology based on BCl 3 and Cl 2 mixed gases to etch the a-axis orientation Zn 1 grown by metal-organic vapor phase epitaxy. - x Mg x O (0≤x≤0.3) films.
(二)湿法刻蚀(2) Wet etching
湿法刻蚀的优势是工艺简单和对薄膜表面的损伤小,其缺点是不易控制侧壁剖面。例如,美国佛罗里达大学J.Chen等人采用基于HCl/H2O和H3PO4/H2O溶液刻蚀脉冲激光沉积法生长的Zn0.9Mg0.1O薄膜。The advantage of wet etching is that the process is simple and the damage to the film surface is small, and its disadvantage is that it is not easy to control the sidewall profile. For example, J.Chen et al., University of Florida, USA used HCl/H 2 O and H 3 PO 4 /H 2 O solution etching pulsed laser deposition to grow Zn 0.9 Mg 0.1 O thin films.
再如,美国Lumenz公司J.Tresback等人采用基于H3PO4/H2O溶液的湿法刻蚀技术刻蚀金属有机气相外延法生长的a轴取向Zn1-xMgxO(0≤x≤0.3)薄膜。For another example, J. Tresback et al. from Lumenz Company of the United States used wet etching technology based on H 3 PO 4 /H 2 O solution to etch a-axis orientation Zn 1-x Mg x O (0≤ x≤0.3) film.
但是,上述研究仅限于在刻蚀a轴择优取向Zn1-xMgxO薄膜过程中刻蚀速率和对薄膜成分的影响,均未涉及侧壁剖面和脊形波导结构的制作。目前国内外尚缺少制作c轴择优取向Zn1-xMgxO(0≤x≤0.3)脊形波导的刻蚀技术。However, the above studies are limited to the etching rate and the effect on the composition of the film during the process of etching the a-axis preferred orientation Zn 1-x Mg x O film, and did not involve the fabrication of sidewall profiles and ridge waveguide structures. At present, there is still a lack of etching technology for fabricating c-axis preferred orientation Zn 1-x Mg x O (0≤x≤0.3) ridge waveguide at home and abroad.
发明内容Contents of the invention
有鉴于此,本发明的主要目的在于提供一种c轴择优取向Zn1-xMgxO脊型波导及其制作方法,以期至少部分地解决上述提及的技术问题中的至少之一。In view of this, the main purpose of the present invention is to provide a c-axis preferred orientation Zn 1-x Mg x O ridge waveguide and its manufacturing method, in order to at least partially solve at least one of the above-mentioned technical problems.
为实现上述目的,本发明的技术方案如下:To achieve the above object, the technical scheme of the present invention is as follows:
作为本发明的一个方面,提供了一种c轴择优取向Zn1-xMgxO脊型波导的制作方法,包括:在c轴择优取向Zn1-xMgxO薄膜上形成条形的掩蔽层,其中0≤x≤0.3;以及在所述掩蔽层的保护下,采用干法刻蚀技术对所述c轴择优取向Zn1-xMgxO薄膜进行刻蚀,形成脊型波导结构。As one aspect of the present invention, there is provided a method for fabricating a Zn 1-x Mg x O ridge waveguide with preferred c-axis orientation, comprising: forming strip-shaped masking on the Zn 1-x Mg x O film with preferred orientation of c-axis layer, wherein 0≤x≤0.3; and under the protection of the mask layer, the c-axis preferred orientation Zn 1-x Mg x O thin film is etched by dry etching technology to form a ridge waveguide structure.
作为本发明的另一个方面,提供了一种通过如上所述的制作方法得到的c轴择优取向Zn1-xMgxO脊形波导。As another aspect of the present invention, a c-axis preferred orientation Zn 1-x Mg x O ridge waveguide obtained by the above-mentioned manufacturing method is provided.
从上述技术方案可以看出,本发明的c轴择优取向Zn1-xMgxO脊型波导及其制作方法至少具有以下有益效果其中之一或其中一部分:It can be seen from the above technical solutions that the c-axis preferred orientation Zn 1-x Mg x O ridge waveguide and its manufacturing method of the present invention have at least one or part of the following beneficial effects:
本发明采用干法刻蚀技术所制作的c轴择优取向Zn1-xMgxO(0≤x≤0.3)脊形波导,利用其二阶非线性光学特性以及脊型波导对传输光的限制,可应用于光波耦合器、波导调制器、波导开关以及波导激光器等无源和有源器件,在集成光学和光互连等领域具有广阔的应用前景。The invention adopts the c-axis preferred orientation Zn 1-x Mg x O (0≤x≤0.3) ridge waveguide produced by dry etching technology, and utilizes its second-order nonlinear optical characteristics and the limitation of the ridge waveguide to the transmitted light , can be applied to passive and active devices such as optical wave couplers, waveguide modulators, waveguide switches, and waveguide lasers, and has broad application prospects in the fields of integrated optics and optical interconnection.
附图说明Description of drawings
图1为本发明实施例1至4的c轴择优取向Zn1-xMgxO(0≤x≤0.3)脊形波导制作方法的流程图;Fig. 1 is the flow chart of the manufacturing method of the c-axis preferential orientation Zn 1-x Mg x O (0≤x≤0.3) ridge waveguide of the
图2为本发明实施例1中ICP-RIE刻蚀中Ar/(Ar+HBr)气体比例对Zn0.72Mg0.28O薄膜刻蚀速率、光刻胶刻蚀速率和刻蚀选择比的影响;Fig. 2 is the influence of Ar/(Ar+HBr) gas ratio on Zn 0.72 Mg 0.28 O film etching rate, photoresist etching rate and etching selectivity ratio in the ICP-RIE etching in the
图3为本发明实施例1中采用Ar/(Ar+HBr)=80%气体比例ICP-RIE刻蚀后Zn0.72Mg0.28O薄膜样品的横截面SEM图片;3 is a cross-sectional SEM image of a Zn 0.72 Mg 0.28 O thin film sample etched by Ar/(Ar+HBr)=80% gas ratio ICP-RIE in Example 1 of the present invention;
图4为本发明实施例2中采用45°样品倾斜角度Ar离子束刻蚀前后Zn0.72Mg0.28O薄膜样品的横截面SEM图片,其中(a)为刻蚀前,(b)为刻蚀后;Fig. 4 is a cross-sectional SEM image of a Zn 0.72 Mg 0.28 O thin film sample before and after etching with an Ar ion beam at a sample tilt angle of 45° in Example 2 of the present invention, wherein (a) is before etching, and (b) is after etching ;
图5为本发明实施例3中采用7°样品倾斜角度Ar离子束刻蚀后Zn1-xMgxO(x=0.11或0.28)薄膜样品的SEM图片,其中,(a)为Zn0.89Mg0.11样品横截面,(b)为Zn0.87Mg0.28O样品。Fig. 5 is the SEM image of the Zn 1-x Mg x O (x=0.11 or 0.28) thin film sample after adopting Ar ion beam etching at a sample tilt angle of 7° in Example 3 of the present invention, wherein (a) is Zn 0.89 Mg 0.11 Sample cross section, (b) is Zn 0.87 Mg 0.28 O sample.
图6为本发明实施例4中先后采用45°和7°样品倾斜角度两步Ar离子束刻蚀后Zn1- xMgxO(x=0.11或0.28)薄膜样品的横截面SEM图片,其中(a)为Zn0.89Mg0.11样品,(b)为Zn0.72Mg0.28O样品。Fig. 6 is the cross-sectional SEM picture of the Zn 1- x Mg x O (x=0.11 or 0.28) film sample after successively adopting 45 ° and 7 ° sample tilt angle two-step Ar ion beam etching in Example 4 of the present invention, wherein (a) is Zn 0.89 Mg 0.11 sample, (b) is Zn 0.72 Mg 0.28 O sample.
具体实施方式Detailed ways
本发明公开了采用干法刻蚀技术,将c轴择优取向Zn1-xMgxO(0≤x≤0.3)薄膜制作成具有1-2微米横向宽度的脊形波导,可应用于基于非线性波导的无源或有源器件,在集成光学和光互连等领域具有广阔的应用前景。The invention discloses a ridge waveguide with a lateral width of 1-2 microns made of a c-axis preferred orientation Zn 1-x Mg x O (0≤x≤0.3) film by dry etching technology, which can be applied to Passive or active devices of linear waveguides have broad application prospects in the fields of integrated optics and optical interconnection.
为使本发明的目的、技术方案和优点更加清楚明白,以下结合具体实施例,并参照附图,对本发明作进一步的详细说明。In order to make the object, technical solution and advantages of the present invention clearer, the present invention will be further described in detail below in conjunction with specific embodiments and with reference to the accompanying drawings.
具体而言,根据本发明的一些实施例,提供了一种c轴择优取向Zn1-xMgxO脊型波导的制作方法,包括步骤S1和步骤S2:Specifically, according to some embodiments of the present invention, a method for fabricating a c-axis preferred orientation Zn 1-x Mg x O ridge waveguide is provided, including step S1 and step S2:
步骤S1:在c轴择优取向Zn1-xMgxO薄膜上形成条形的掩蔽层,其中0≤x≤0.3;以及Step S1: forming a strip-shaped masking layer on the c-axis preferred orientation Zn 1-x Mg x O film, where 0≤x≤0.3; and
步骤S2:在掩蔽层的保护下,采用干法刻蚀技术对该c轴择优取向Zn1-xMgxO薄膜进行刻蚀,形成脊型波导结构。Step S2: under the protection of the mask layer, the c-axis preferred orientation Zn 1-x Mg x O thin film is etched by dry etching technology to form a ridge waveguide structure.
在一些实施例中,步骤S1的c轴择优取向Zn1-xMgxO薄膜的厚度为500~600nm,优选为500nm。依据平板波导模式理论,500nm薄厚是Zn0.72Mg0.28O薄膜(1550nm波长处折射率为1.87)作为波导芯层传输单模式光所需的最低厚度。另外,薄厚过大(>600nm)会导致Zn1- xMgxO薄膜的生长质量变差而增大传输损耗。In some embodiments, the thickness of the c-axis preferentially oriented Zn 1-x Mg x O film in step S1 is 500-600 nm, preferably 500 nm. According to the theory of slab waveguide mode, the thickness of 500nm is the minimum thickness required for Zn 0.72 Mg 0.28 O film (refractive index at 1550nm wavelength is 1.87) as the waveguide core layer to transmit single-mode light. In addition, if the thickness is too large (>600nm), the growth quality of the Zn 1- x Mg x O film will deteriorate and the transmission loss will increase.
在一些实施例中,该c轴择优取向Zn1-xMgxO薄膜为采用射频磁控溅射法在热氧化Si(100)衬底(以下简称为SiO2/Si衬底)上形成,热氧化层厚度为2000-3000nm。其中Mg的组成x控制在0.3以下,有利于保持纤锌矿型晶体结构。In some embodiments, the c-axis preferred orientation Zn 1-x Mg x O film is formed on a thermally oxidized Si(100) substrate (hereinafter referred to as SiO 2 /Si substrate) by radio frequency magnetron sputtering, The thickness of the thermal oxide layer is 2000-3000nm. The composition x of Mg is controlled below 0.3, which is conducive to maintaining the wurtzite crystal structure.
在一些实施例中,对于步骤S2所采用的不同干法刻蚀技术,步骤S1中可以采用不同的方法和材料制作掩蔽层;掩蔽层的厚度要具体依据刻蚀深度和刻蚀选择比而确定。In some embodiments, for the different dry etching techniques used in step S2, different methods and materials can be used to make the masking layer in step S1; the thickness of the masking layer is determined according to the etching depth and etching selection ratio. .
具体地,掩蔽层可以是采用旋涂法制备的光刻胶层,干法刻蚀技术为基于HBr和Ar混合气体的电感耦合等离子体增强反应离子(以下简称ICP-RIE)刻蚀技术,该刻蚀气体有利于提高薄膜侧壁坡度。此时可以获得最高为0.2的刻蚀选择比和最大约为60°的侧壁坡度,适于制作浅脊波导结构。Specifically, the masking layer may be a photoresist layer prepared by a spin coating method, and the dry etching technology is an inductively coupled plasma enhanced reactive ion (ICP-RIE) etching technology based on a mixed gas of HBr and Ar. The etchant gas is beneficial to increase the slope of the film sidewall. At this time, an etching selectivity ratio of up to 0.2 and a sidewall slope of up to about 60° can be obtained, which is suitable for making a shallow ridge waveguide structure.
或者,掩蔽层可以是采用等离子体增强化学沉积法(以下简称PECVD)形成的SiO2层,干法刻蚀技术为Ar离子束刻蚀技术。此时可以获得最高约为0.8的刻蚀选择比和最大接近90°的侧壁坡度,适于制作深脊波导结构。Alternatively, the masking layer may be a SiO 2 layer formed by plasma enhanced chemical deposition (hereinafter referred to as PECVD), and the dry etching technique is Ar ion beam etching technique. At this time, a maximum etching selectivity of about 0.8 and a maximum sidewall slope of approximately 90° can be obtained, which is suitable for making a deep ridge waveguide structure.
在一些实施例中,掩蔽层为采用旋涂法制备的光刻胶层时,步骤S1具体包括:In some embodiments, when the masking layer is a photoresist layer prepared by spin coating, step S1 specifically includes:
使用光刻版和光刻胶经光刻工艺在该c轴择优取向Zn1-xMgxO薄膜上制作条形的光刻胶掩蔽层。A strip-shaped photoresist masking layer is fabricated on the c-axis preferred orientation Zn 1-x Mg x O film through a photolithography process using a photolithography plate and a photoresist.
在一些实施例中,掩蔽层为采用PECVD形成的SiO2层时,步骤S1具体包括子步骤S11~S13:In some embodiments, when the masking layer is a SiO2 layer formed by PECVD, step S1 specifically includes sub-steps S11-S13:
子步骤S11,采用等离子体增强化学沉积法在该c轴择优取向Zn1-xMgxO薄膜上淀积一层SiO2层;Sub-step S11, depositing a layer of SiO 2 on the c-axis preferred orientation Zn 1-x Mg x O thin film by plasma enhanced chemical deposition;
子步骤S12,使用光刻版和光刻胶经光刻工艺在该SiO2层上形成条形的光刻胶掩蔽层;以及Sub-step S12, using a photolithography plate and a photoresist to form a strip-shaped photoresist masking layer on the SiO2 layer through a photolithography process; and
子步骤S13,在该光刻胶掩蔽层的保护下,采用反应离子刻蚀技术对SiO2层进行刻蚀,形成条形的SiO2掩蔽层。In sub-step S13 , under the protection of the photoresist mask layer, the SiO 2 layer is etched by reactive ion etching technology to form a strip-shaped SiO 2 mask layer.
可选的,上述光刻工艺例如可以包括氧等离子体表面处理、蒸粘结剂、甩胶、前烘、紫外光刻、坚膜和氧等离子体去底胶等步骤。Optionally, the above-mentioned photolithography process may include, for example, steps such as oxygen plasma surface treatment, adhesive evaporation, glue spin, prebaking, ultraviolet lithography, film hardening, and oxygen plasma primer removal.
在一些实施例中,在步骤S1之前还包括:将c轴择优取向Zn1-xMgxO薄膜在丙酮溶剂、无水酒精溶剂、超纯水中清洗,然后进行干燥。具体地,清洗时间分别为5分钟,干燥操作依次包括经氮气吹干以及在120℃下烘干。In some embodiments, before step S1, it further includes: washing the c-axis preferentially oriented Zn 1-x Mg x O film in acetone solvent, absolute alcohol solvent, and ultrapure water, and then drying. Specifically, the cleaning time is 5 minutes respectively, and the drying operation sequentially includes blowing dry with nitrogen and drying at 120°C.
在一些实施例中,步骤S2的ICP-RIE刻蚀技术的工艺参数包括:向刻蚀腔中通入HBr和Ar的混合气体(气体比例20%-80%),流量范围在15-25sccm之间,气压范围在3-7mTorr之间,ICP功率范围在500-1000W之间,射频功率范围在250-500W之间,直流偏压范围在150-250V之间。In some embodiments, the process parameters of the ICP-RIE etching technique in step S2 include: a mixed gas of HBr and Ar (
在一些实施例中,步骤S2的Ar离子束刻蚀处理的工艺参数包括:向刻蚀腔中通入Ar气体,流量范围在15-25sccm之间,气压范围在0.5-1.5Pa之间,样品倾斜角度范围在5-60°之间,样品转速范围在5-10rpm之间,束电压范围在100-500V之间,束电流范围在50-150mA之间。In some embodiments, the process parameters of the Ar ion beam etching treatment in step S2 include: feeding Ar gas into the etching chamber, the flow range is between 15-25 sccm, the gas pressure range is between 0.5-1.5Pa, and the sample The tilt angle range is between 5-60°, the sample rotation speed range is between 5-10rpm, the beam voltage range is between 100-500V, and the beam current range is between 50-150mA.
在一些实施例中,在步骤S2采用Ar离子束刻蚀技术时,可进一步采用分步刻蚀c轴择优取向Zn1-xMgxO薄膜,并且在分步刻蚀中逐步减小样品倾斜角度。本发明的“样品倾斜角度”也即为Ar离子束与c轴择优取向Zn1-xMgxO薄膜样品的衬底表面法线的夹角。In some embodiments, when the Ar ion beam etching technique is used in step S2, the c-axis preferred orientation Zn 1-x Mg x O film can be further etched step by step, and the sample tilt can be gradually reduced in the step S2 angle. The "sample tilt angle" in the present invention is also the angle between the Ar ion beam and the normal line of the substrate surface of the c-axis preferred orientation Zn 1-x Mg x O thin film sample.
举例而言,分为三步对c轴择优取向Zn1-xMgxO薄膜进行刻蚀时,第一步采用60°样品倾斜角度,第二步采用45°样品倾斜角度,第三步采用7°样品倾斜角度等,但并不局限于此。For example, when etching a c-axis preferentially oriented Zn 1-x Mg x O film in three steps, the first step uses a sample tilt angle of 60°, the second step uses a sample tilt angle of 45°, and the third step uses 7° sample tilt angle, etc., but not limited thereto.
在SiO2掩蔽层保护下,采用Ar离子束分步刻蚀c轴择优取向Zn1-xMgxO薄膜,可同时实现最高为0.99的刻蚀选择比,侧壁坡度大范围可控,且有利于去除SiO2掩蔽层。Under the protection of SiO 2 masking layer, using Ar ion beam to etch the c-axis preferred orientation Zn 1-x Mg x O film step by step, the highest etching selectivity ratio of 0.99 can be realized at the same time, the sidewall slope can be controlled in a wide range, and Facilitates the removal of the SiO2 masking layer.
根据本发明的一些实施例,还提供了一种通过上述制作方法得到的c轴择优取向Zn1-xMgxO脊形波导,具有1-2微米横向宽度。According to some embodiments of the present invention, there is also provided a c-axis preferred orientation Zn 1-x Mg x O ridge waveguide obtained by the above manufacturing method, with a lateral width of 1-2 microns.
以下列举多个具体实施例来对本发明的技术方案作详细说明。需要说明的是,下文中的具体实施例仅用于示例,并不用于限制本发明。A number of specific embodiments are listed below to describe the technical solution of the present invention in detail. It should be noted that the following specific embodiments are only for illustration, and are not intended to limit the present invention.
实施例1:Example 1:
图1为本发明实施例1的c轴择优取向Zn1-xMgxO(0≤x≤0.3)脊形波导制作方法的流程图,如图1所示,本实施例的制作方法包括:Fig. 1 is the flow chart of the manufacturing method of the c-axis preferential orientation Zn 1-x Mg x O (0≤x≤0.3) ridge waveguide of the
步骤A,清洗Zn1-xMgxO(0≤x≤0.3)薄膜样品(薄膜厚度约500nm),Zn1-xMgxO薄膜采用射频磁控溅射法在SiO2/Si衬底上形成。Step A, cleaning Zn 1-x Mg x O (0≤x≤0.3) thin film sample (film thickness about 500nm), Zn 1-x Mg x O thin film on SiO 2 /Si substrate by radio frequency magnetron sputtering form.
步骤B,使用光刻版(Cr条宽和周期分别约为1700nm和100μm)和某公司光刻胶(型号AZ6130),经过氧等离子体表面处理、蒸粘结剂、甩胶、前烘、紫外光刻、坚膜和氧等离子体去底胶等步骤,在步骤A清洗后的Zn1-xMgxO(0≤x≤0.3)薄膜的表面上制作周期排列条形光刻胶掩蔽层(厚度约为1000nm,横向宽度约为1700nm,周期约为100μm)。Step B, using a photolithography plate (the width and period of Cr strips are about 1700nm and 100μm respectively) and a certain company’s photoresist (model AZ6130), after oxygen plasma surface treatment, steaming adhesive, glue rejection, pre-baking, and ultraviolet light Steps such as photolithography, film hardening and oxygen plasma primer removal, on the surface of the Zn 1-x Mg x O (0≤x≤0.3) film after step A cleaning, make periodic array strip photoresist masking layer ( The thickness is about 1000nm, the lateral width is about 1700nm, and the period is about 100μm).
步骤C,采用基于HBr和Ar混合气体的ICP-RIE技术加工Zn1-xMgxO(0≤x≤0.3)浅脊波导结构。采用表1中列出的ICP-RIE设备参数处理Zn1-xMgxO薄膜。In step C, the Zn 1-x Mg x O (0≤x≤0.3) shallow ridge waveguide structure is processed by ICP-RIE technology based on the mixed gas of HBr and Ar. The Zn 1-x Mg x O thin films were processed using the ICP-RIE equipment parameters listed in Table 1.
表1 ICP-RIE设备设置参数Table 1 ICP-RIE equipment setting parameters
图2为本发明实施例1中ICP-RIE刻蚀中Ar/(Ar+HBr)气体比例(20%、50%和80%)对Zn0.72Mg0.28O薄膜刻蚀速率、光刻胶掩蔽层刻蚀速率及刻蚀选择比的影响。随着Ar气体含量的增加,Zn0.72Mg0.28O薄膜和光刻胶掩蔽层的刻蚀速率逐渐下降,但是刻蚀选择比有所增加。当Ar/(Ar+HBr)气体比例为80%时,Zn0.72Mg0.28O薄膜和光刻胶掩蔽层的刻蚀速率分别为19.6nm/min和102.8nm/min,刻蚀选择比达到最大值(约为0.2)。Fig. 2 is the ratio of Ar/(Ar+HBr) gas (20%, 50% and 80%) in ICP-RIE etching in the
图3为本发明实施例1中采用Ar/(Ar+HBr)=80%气体比例ICP-RIE刻蚀后Zn0.72Mg0.28O薄膜样品的横截面SEM图片。在刻蚀后,Zn0.72Mg0.28O薄膜的剖面呈现浅脊形结构,脊形侧壁坡度约为60°。采用原子力显微镜测定脊部表面的均方根粗糙度(σrms)约为1.8nm。3 is a cross-sectional SEM image of a Zn 0.72 Mg 0.28 O thin film sample etched by ICP-RIE with Ar/(Ar+HBr)=80% gas ratio in Example 1 of the present invention. After etching, the profile of the Zn 0.72 Mg 0.28 O film presents a shallow ridge structure, and the slope of the ridge sidewall is about 60°. The root-mean-square roughness (σ rms ) of the surface of the ridge was measured by an atomic force microscope to be about 1.8 nm.
实施例2:Example 2:
如图1所示,本实施例的制作方法包括:As shown in Figure 1, the production method of this embodiment includes:
步骤A,清洗Zn1-xMgxO(x=0.11或0.28)薄膜(薄膜厚度约500nm)样品,Zn1-xMgxO薄膜采用射频磁控溅射法在SiO2/Si衬底上形成。Step A, cleaning Zn 1-x Mg x O (x=0.11 or 0.28) thin film (film thickness about 500nm) sample, Zn 1-x Mg x O thin film adopts radio frequency magnetron sputtering method on SiO 2 /Si substrate form.
步骤B,采用PECVD方法在步骤A清洗后的Zn1-xMgxO(x=0.11或0.28)薄膜的表面上淀积一层SiO2薄膜(厚度约为1000nm)。使用光刻版(Cr条宽和周期分别为1700nm和100μm)和某公司光刻胶(型号AZ6130),经过氧等离子体表面处理、蒸粘结剂、甩胶、前烘、紫外光刻、坚膜和氧等离子体去底胶等步骤,在SiO2/Zn1-xMgxO(x=0.11或0.28)样品的表面上制作周期排列条形光刻胶掩蔽层(厚度约为1000nm,横向宽度约为1700nm,周期约为100μm)。采用反应离子刻蚀技术,在Zn1-xMgxO(x=0.11或0.28)样品的表面上制作周期排列条形SiO2掩蔽层(厚度约为1000nm,横向宽度约为1700nm,周期约为100μm)。In step B, a layer of SiO 2 film (about 1000 nm in thickness) is deposited on the surface of the Zn 1-x Mg x O (x=0.11 or 0.28) film cleaned in step A by PECVD method. Using a photolithography plate (Cr strip width and period are 1700nm and 100μm respectively) and a company’s photoresist (model AZ6130), after oxygen plasma surface treatment, steaming binder, glue rejection, pre-baking, ultraviolet lithography, hardening film and oxygen plasma to remove primer and other steps, on the surface of SiO 2 /Zn 1-x Mg x O (x=0.11 or 0.28) samples, make a periodic array of strip photoresist masking layers (thickness is about 1000nm, lateral The width is about 1700nm and the period is about 100μm). Using reactive ion etching technology, on the surface of Zn 1-x Mg x O (x = 0.11 or 0.28) samples, fabricate a periodically arranged strip-shaped SiO 2 masking layer (thickness is about 1000nm, lateral width is about 1700nm, period is about 100μm).
步骤C,采用Ar离子束刻蚀技术加工Zn1-xMgxO(x=0.11或0.28)深脊波导结构。采用表2中列出的Ar离子束刻蚀设备参数处理Zn1-xMgxO薄膜。Step C, processing the Zn 1-x Mg x O (x=0.11 or 0.28) deep ridge waveguide structure by Ar ion beam etching technology. The parameters of the Ar ion beam etching equipment listed in Table 2 were used to process the Zn 1-x Mg x O thin films.
表2 Ar离子束刻蚀设备设置参数Table 2 Ar ion beam etching equipment setting parameters
图4为本发明实施例2中采用45°样品倾斜角度Ar离子束刻蚀前后Zn0.72Mg0.28O薄膜(初始厚度约100nm)样品的横截面SEM图片。如图4(a)所示,经反应离子刻蚀后,在Zn0.72Mg0.28O薄膜的表面形成侧壁坡度接近90°的SiO2掩蔽层。如图4(b)所示,经Ar离子束刻蚀后,未被SiO2掩蔽层覆盖的Zn0.72Mg0.28O薄膜被完全刻蚀掉,形成条形结构,刻蚀速率约为11.4nm/min。同时,刻蚀形成的脊形侧壁坡度接近90°。另外,在Zn0.72Mg0.28O条形结构上方的SiO2掩蔽层部分被刻蚀掉,其侧壁坡度依然保持90°。SiO2掩蔽层的刻蚀速率约为28.1nm/min,刻蚀选择比约为0.41。但是,在Zn0.72Mg0.28O薄膜下面的热氧化SiO2层也被刻蚀,在Zn0.72Mg0.28O脊形的下面形成小坡度脊形。Fig. 4 is a cross-sectional SEM picture of a Zn 0.72 Mg 0.28 O film (initial thickness about 100 nm) sample before and after etching with an Ar ion beam at a sample tilt angle of 45° in Example 2 of the present invention. As shown in Figure 4(a), after reactive ion etching, a SiO 2 masking layer with a sidewall slope close to 90° is formed on the surface of the Zn 0.72 Mg 0.28 O film. As shown in Fig. 4(b), after Ar ion beam etching, the Zn 0.72 Mg 0.28 O film not covered by the SiO 2 masking layer was completely etched away, forming a stripe structure, and the etching rate was about 11.4nm/ min. At the same time, the slope of the ridge-shaped sidewall formed by etching is close to 90°. In addition, part of the SiO 2 masking layer above the Zn 0.72 Mg 0.28 O strips was etched away, and the sidewall slope remained at 90°. The etch rate of the SiO 2 mask layer is about 28.1nm/min, and the etch selectivity is about 0.41. However, the thermally oxidized SiO2 layer under the Zn 0.72 Mg 0.28 O film was also etched, forming a small-slope ridge underneath the Zn 0.72 Mg 0.28 O ridge.
实施例3:Example 3:
如图1所示,本实施例的制作方法包括:As shown in Figure 1, the production method of this embodiment includes:
步骤A,清洗Zn1-xMgxO(x=0.11或0.28)薄膜(薄膜厚度约为500nm)样品,Zn1-xMgxO薄膜采用射频磁控溅射法在SiO2/Si衬底上形成。Step A, cleaning Zn 1-x Mg x O (x=0.11 or 0.28) film (film thickness is about 500nm) sample, Zn 1-x Mg x O film adopts radio frequency magnetron sputtering method on SiO 2 /Si substrate Formed on.
步骤B,采用PECVD方法在步骤A清洗后的Zn1-xMgxO(x=0.11或0.28)薄膜的表面上淀积一层SiO2薄膜(厚度约为1000nm)。使用光刻版(Cr条宽和周期分别为1700nm和100μm)和某公司光刻胶(型号AZ6130),经过氧等离子体表面处理、蒸粘结剂、甩胶、前烘、紫外光刻、坚膜和氧等离子体去底胶等步骤,在SiO2/Zn1-xMgxO(x=0.11或0.28)样品的表面上制作周期排列条形光刻胶掩蔽层(厚度约为1000nm,横向宽度约为1700nm,周期约为100μm)。采用反应离子刻蚀技术,在Zn1-xMgxO(x=0.11或0.28)样品的表面上制作周期排列条形SiO2掩蔽层(厚度约为1000nm,横向宽度约为1700nm,周期约为100μm)。In step B, a layer of SiO 2 film (about 1000 nm in thickness) is deposited on the surface of the Zn 1-x Mg x O (x=0.11 or 0.28) film cleaned in step A by PECVD method. Using a photolithography plate (Cr strip width and period are 1700nm and 100μm respectively) and a company’s photoresist (model AZ6130), after oxygen plasma surface treatment, steaming binder, glue rejection, pre-baking, ultraviolet lithography, hardening film and oxygen plasma to remove primer and other steps, on the surface of SiO 2 /Zn 1-x Mg x O (x=0.11 or 0.28) samples, make a periodic array of strip photoresist masking layers (thickness is about 1000nm, lateral The width is about 1700nm and the period is about 100μm). Using reactive ion etching technology, on the surface of Zn 1-x Mg x O (x = 0.11 or 0.28) samples, fabricate a periodically arranged strip-shaped SiO 2 masking layer (thickness is about 1000nm, lateral width is about 1700nm, period is about 100μm).
步骤C,采用Ar离子束刻蚀技术加工Zn1-xMgxO(x=0.11或0.28)深脊波导结构。采用表3中列出的Ar离子束刻蚀设备参数处理Zn1-xMgxO薄膜。Step C, processing the Zn 1-x Mg x O (x=0.11 or 0.28) deep ridge waveguide structure by Ar ion beam etching technology. The parameters of the Ar ion beam etching equipment listed in Table 3 were used to process the Zn 1-x Mg x O thin films.
表3 Ar离子束刻蚀设备设置参数Table 3 Ar ion beam etching equipment setting parameters
图5为本发明实施例3中采用7°样品倾斜角度Ar离子束刻蚀后Zn1-xMgxO(x=0.11或0.28)(初始厚度约500nm)样品的横截面SEM图片。如图5(a)所示,经Ar离子束刻蚀后,未被SiO2掩蔽层覆盖的Zn0.89Mg0.11O薄膜被完全刻蚀掉,形成深脊结构,刻蚀速率约为18.4nm/min。同时,刻蚀形成的条形侧壁坡度约60°。此外,在Zn0.89Mg0.11O深脊结构上方的SiO2掩蔽层被刻蚀成三角形,中间部位的刻蚀约为13.0nm/min,刻蚀选择比约为1.42。如图5(b)所示,未被SiO2掩蔽层覆盖的Zn0.87Mg0.28O薄膜大部分被刻蚀掉,形成深脊结构,刻蚀速率约为12.6nm/min。同时,刻蚀形成的脊形侧壁坡度接近90°。另外,在侧壁坡度接近90°的深脊形下方未形成如图4(b)中的小坡度脊形。此外,在Zn0.87Mg0.28O深脊结构上方的SiO2掩蔽层被刻蚀成三角形,中间部位的刻蚀约为16.3nm/min,刻蚀选择比约为0.77。这些结果表明:(1)Zn1-xMgxO薄膜中的Mg含量影响Ar离子束刻蚀速率和侧壁坡度。(2)样品倾斜角度影响Zn1- xMgxO脊形结构上方的SiO2掩蔽层和其下方的热氧化SiO2层的形状。5 is a cross-sectional SEM image of a Zn 1-x Mg x O (x=0.11 or 0.28) (initial thickness of about 500 nm) sample etched by an Ar ion beam at a sample tilt angle of 7° in Example 3 of the present invention. As shown in Fig. 5(a), after Ar ion beam etching, the Zn 0.89 Mg 0.11 O film not covered by the SiO 2 masking layer is completely etched away, forming a deep ridge structure, and the etching rate is about 18.4nm/ min. At the same time, the strip-shaped sidewall slope formed by etching is about 60°. In addition, the SiO 2 masking layer above the Zn 0.89 Mg 0.11 O deep ridge structure is etched into a triangle shape, the etching in the middle part is about 13.0nm/min, and the etching selectivity is about 1.42. As shown in Figure 5(b), most of the Zn 0.87 Mg 0.28 O film not covered by the SiO 2 masking layer was etched away, forming a deep ridge structure, and the etching rate was about 12.6nm/min. At the same time, the slope of the ridge-shaped sidewall formed by etching is close to 90°. In addition, the small-slope ridges as shown in Fig. 4(b) are not formed under the deep ridges whose sidewall slopes are close to 90°. In addition, the SiO 2 masking layer above the Zn 0.87 Mg 0.28 O deep ridge structure is etched into a triangle shape, the etching in the middle part is about 16.3nm/min, and the etching selectivity is about 0.77. These results show that: (1) The Mg content in the Zn 1-x Mg x O films affects the Ar ion beam etching rate and sidewall slope. (2) The sample tilt angle affects the shape of the SiO2 masking layer above the Zn1 - xMgxO ridge structure and the thermally oxidized SiO2 layer below it.
实施例4:Example 4:
如图1所示,本实施例的制作方法包括:As shown in Figure 1, the production method of this embodiment includes:
步骤A,清洗Zn1-xMgxO(x=0.11或0.28)薄膜(薄膜厚度约为500nm)样品,Zn1-xMgxO薄膜采用射频磁控溅射法在SiO2/Si衬底上形成。Step A, cleaning Zn 1-x Mg x O (x=0.11 or 0.28) film (film thickness is about 500nm) sample, Zn 1-x Mg x O film adopts radio frequency magnetron sputtering method on SiO 2 /Si substrate Formed on.
步骤B,采用PECVD方法在步骤A清洗后的Zn1-xMgxO(x=0.11或0.28)薄膜的表面上淀积一层SiO2薄膜(厚度约为1000nm)。使用光刻版(Cr条宽和周期分别为1700nm和100μm)和某公司光刻胶(型号AZ6130),经过氧等离子体表面处理、蒸粘结剂、甩胶、前烘、紫外光刻、坚膜和氧等离子体去底胶等步骤,在SiO2/Zn1-xMgxO(x=0.11或0.28)样品的表面上制作周期排列条形光刻胶掩蔽层(厚度约为1000nm,横向宽度约为1700nm,周期约为100μm)。采用反应离子刻蚀技术,在Zn1-xMgxO(x=0.11或0.28)样品的表面上制作周期排列条形SiO2掩蔽层(厚度约为1000nm,横向宽度约为1700nm,周期约为100μm)。In step B, a layer of SiO 2 film (about 1000 nm in thickness) is deposited on the surface of the Zn 1-x Mg x O (x=0.11 or 0.28) film cleaned in step A by PECVD method. Using a photolithography plate (Cr strip width and period are 1700nm and 100μm respectively) and a company’s photoresist (model AZ6130), after oxygen plasma surface treatment, steaming binder, glue rejection, pre-baking, ultraviolet lithography, hardening film and oxygen plasma to remove primer and other steps, on the surface of SiO 2 /Zn 1-x Mg x O (x=0.11 or 0.28) samples, make a periodic array of strip photoresist masking layers (thickness is about 1000nm, lateral The width is about 1700nm and the period is about 100μm). Using reactive ion etching technology, on the surface of Zn 1-x Mg x O (x = 0.11 or 0.28) samples, fabricate a periodically arranged strip-shaped SiO 2 masking layer (thickness is about 1000nm, lateral width is about 1700nm, period is about 100μm).
步骤C,采用Ar离子束刻蚀技术加工Zn1-xMgxO(x=0.11或0.28)深脊波导结构。此次工艺分为两步。第一步采用45°样品倾斜角度,而第二步采用7°样品倾斜角度。采用表4中列出的Ar离子束刻蚀设备参数处理Zn1-xMgxO薄膜。Step C, processing the Zn 1-x Mg x O (x=0.11 or 0.28) deep ridge waveguide structure by Ar ion beam etching technology. This process is divided into two steps. The first step uses a 45° sample tilt angle, while the second step uses a 7° sample tilt angle. The parameters of the Ar ion beam etching equipment listed in Table 4 were used to process the Zn 1-x Mg x O thin films.
表4 Ar离子束刻蚀设备设置参数Table 4 Ar ion beam etching equipment setting parameters
图6为本发明实施例4中两步Ar离子束刻蚀后Zn1-xMgxO(x=0.11或0.28)(初始厚度约500nm)样品的横截面SEM图片。经反应离子刻蚀后,在SiO2掩蔽层的下面形成浅脊结构,脊形侧壁坡度接近90°。Zn0.89Mg0.11O薄膜的刻蚀速率(13.8nm/min)大于Zn0.72Mg0.28O薄膜的刻蚀速率(9.7nm/min)。另外,在Zn0.89Mg0.11O脊形结构上方的SiO2掩蔽层部分被刻蚀掉,其上方两侧边角被消去,呈现类圆弧状,其侧壁坡度依然保持90°。SiO2掩蔽层的刻蚀速率约为14nm/min。其对于Zn0.89Mg0.11O和Zn0.72Mg0.28O薄膜的刻蚀选择比分别约为0.99和0.69。但是,在远离脊形区域,Zn1-xMgxO(x=0.11或0.28)薄膜的刻蚀速率增大,导致在侧壁坡度接近90°的浅脊形下方形成小坡度脊形。这些结果表明:(1)Zn1-xMgxO薄膜中的Mg含量影响Ar离子束刻蚀速率。(2)样品倾斜角度影响Zn1-xMgxO脊形结构上方的SiO2掩蔽层和其下方的热氧化SiO2层的形状。这些结果揭示:采用PECVD法生长的SiO2作为掩蔽层,通过多步变样品倾斜角度的Ar离子束刻蚀Zn1-xMgxO(0≤x≤0.3)薄膜,可同时实现约为0.99的刻蚀选择比、侧壁坡度大范围可控和在维持侧壁坡度接近90°的同时去除SiO2掩蔽层。6 is a cross-sectional SEM image of a Zn 1-x Mg x O (x=0.11 or 0.28) (initial thickness of about 500 nm) sample after two-step Ar ion beam etching in Example 4 of the present invention. After reactive ion etching, a shallow ridge structure is formed under the SiO 2 masking layer, and the slope of the ridge sidewall is close to 90°. The etching rate (13.8nm/min) of Zn 0.89 Mg 0.11 O film is higher than that of Zn 0.72 Mg 0.28 O film (9.7nm/min). In addition, part of the SiO 2 masking layer above the Zn 0.89 Mg 0.11 O ridge structure is etched away, and the corners on both sides above it are eliminated, showing a similar arc shape, and the slope of the side wall is still maintained at 90°. The etch rate of the SiO 2 masking layer is about 14nm/min. Its etching selectivity for Zn 0.89 Mg 0.11 O and Zn 0.72 Mg 0.28 O films is about 0.99 and 0.69, respectively. However, the etch rate of the Zn 1-x Mg x O (x=0.11 or 0.28) film increases in the region away from the ridge, resulting in the formation of a small-slope ridge below the shallow ridge with a sidewall slope close to 90°. These results show that: (1) The Mg content in Zn 1-x Mg x O thin films affects the etching rate of Ar ion beam. (2) The sample tilt angle affects the shape of the SiO2 masking layer above the Zn1 - xMgxO ridge structure and the thermally oxidized SiO2 layer below it. These results reveal that: using SiO 2 grown by PECVD as a mask layer, Zn 1-x Mg x O (0≤x≤0.3) films can be etched by Ar ion beams with multi-step sample tilt angles, and about 0.99 The etch selectivity ratio, the sidewall slope can be controlled in a wide range, and the SiO 2 masking layer can be removed while maintaining the sidewall slope close to 90°.
本发明所制作的c轴择优取向Zn1-xMgxO(0≤x≤0.3)脊形波导可应用于非线性波导、光波耦合器、波导调制器、波导开关以及波导激光器等无源和有源器件,在集成光学和光互连等领域具有广阔的应用前景,对硅基光电子集成芯片等信息技术的发展具有重要的推动作用。The c-axis preferred orientation Zn 1-x Mg x O (0≤x≤0.3) ridge waveguide produced by the present invention can be applied to passive and passive devices such as nonlinear waveguides, optical wave couplers, waveguide modulators, waveguide switches, and waveguide lasers. Active devices have broad application prospects in the fields of integrated optics and optical interconnection, and play an important role in promoting the development of silicon-based optoelectronic integrated chips and other information technologies.
以上所述的具体实施例,对本发明的目的、技术方案和有益效果进行了进一步详细说明,应理解的是,以上所述仅为本发明的具体实施例而已,并不用于限制本发明,凡在本发明的精神和原则之内,所做的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。The specific embodiments described above have further described the purpose, technical solutions and beneficial effects of the present invention in detail. It should be understood that the above descriptions are only specific embodiments of the present invention, and are not intended to limit the present invention. Within the spirit and principles of the present invention, any modifications, equivalent replacements, improvements, etc., shall be included in the protection scope of the present invention.
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110562784.7A CN115373072A (en) | 2021-05-21 | 2021-05-21 | C-axis preferred orientation zinc-magnesium oxide ridge waveguide and manufacturing method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110562784.7A CN115373072A (en) | 2021-05-21 | 2021-05-21 | C-axis preferred orientation zinc-magnesium oxide ridge waveguide and manufacturing method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN115373072A true CN115373072A (en) | 2022-11-22 |
Family
ID=84059719
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110562784.7A Pending CN115373072A (en) | 2021-05-21 | 2021-05-21 | C-axis preferred orientation zinc-magnesium oxide ridge waveguide and manufacturing method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN115373072A (en) |
-
2021
- 2021-05-21 CN CN202110562784.7A patent/CN115373072A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US9625627B2 (en) | Incident angle insensitive color filter and its manufacturing method | |
CN1243286C (en) | Method for producing polymer light wave guide device based on silicon lining | |
CN113687466B (en) | Lithium niobate thin film photon chip based on metal hard mask and processing method thereof | |
Lee et al. | Low-loss GaInAsP wire waveguide on Si substrate with benzocyclobutene adhesive wafer bonding for membrane photonic circuits | |
WO2024104022A1 (en) | Waveguide structure having core-cladding electro-optic material layer, preparation method, and application | |
US6902871B2 (en) | Method for manufacturing polymer microstructures and polymer waveguides | |
CN110320600A (en) | A kind of optical waveguide and its manufacturing method | |
CN115373072A (en) | C-axis preferred orientation zinc-magnesium oxide ridge waveguide and manufacturing method thereof | |
CN113387318B (en) | Near-infrared band-pass filter based on nano annular array and preparation method thereof | |
CN115356806A (en) | An etching method capable of controlling the inclination angle of the sidewall of lithium niobate waveguide | |
CN108878595B (en) | Substrate, semiconductor device and substrate manufacturing method | |
Kilicaslan et al. | Technological challenges in the development of silica-titania platform for integrated optics | |
CN113031151A (en) | Chalcogenide slit optical waveguide structure and preparation method thereof | |
EP3519161B1 (en) | Process for the production of an organized network of nanowires on a metallic substrate | |
KR100361097B1 (en) | Fabricating method of optical waveguide using inductively coupled plasma etcher | |
TWI830101B (en) | Method for dry-etching lithium niobate | |
CN1261780C (en) | Cubic MgZnO crystal thin film optical waveguide device and preparation process thereof | |
CN1778991A (en) | Selective silicon nitrogen oxide sculpturing liquid by wetting method | |
Vojs et al. | Optimization of SiON/SiOx structures fabrication process for optical waveguides | |
CN119200094A (en) | Single-mode micro-disk resonant device and preparation method and application thereof | |
CN102280374B (en) | Manufacturing method of silicon gate structure with thickness of 50nm or less | |
Ji et al. | Highly Integrated Polarization Beam Splitter with MMI Structure Based on LNOI-SiN Rib Waveguide | |
CN117950265A (en) | Lithium niobate nanostructure and its preparation method and application | |
CN116224494A (en) | Manufacturing method of lithium niobate ridge waveguide and photoelectric device | |
CN115016063A (en) | Sub-nanometer precision waveguide process for step-by-step etching by double-layer glue mask |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |