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CN101819296B - Method for preparing polysiloxane optical waveguide for optical interconnection - Google Patents

Method for preparing polysiloxane optical waveguide for optical interconnection Download PDF

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CN101819296B
CN101819296B CN2010101179097A CN201010117909A CN101819296B CN 101819296 B CN101819296 B CN 101819296B CN 2010101179097 A CN2010101179097 A CN 2010101179097A CN 201010117909 A CN201010117909 A CN 201010117909A CN 101819296 B CN101819296 B CN 101819296B
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trimethylsiloxy
tetrakis
silane
optical waveguide
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CN101819296A (en
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季家镕
窦文华
冯向华
温昌礼
宋艳生
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National University of Defense Technology
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Abstract

本发明公开了一种用于光互连的聚硅氧烷光波导的制备方法,目的是提供一种制备长度大于20cm,成本低的用于光互连的光波导制备方法。技术方案是设计光波导图样,制得模板;将聚偏二氟乙烯溶液涂覆在模版上,脱模得到翻版;用苯基甲基环硅氧烷混合液填充翻版中的凹槽,苯基甲基环硅氧烷混合液固化后成为脊型波导的芯层;把四(三甲基甲硅烷氧基)硅烷混合液涂覆在翻版上,烘烤后形成四(三甲基甲硅烷氧基)硅烷薄膜;将翻版从四(三甲基甲硅烷氧基)硅烷薄膜上剥离,四(三甲基甲硅烷氧基)硅烷薄膜形成下包层;将四(三甲基甲硅烷氧基)硅烷混合液涂覆在脊形波导上,四(三甲基甲硅烷氧基)硅烷混合液固化,形成聚合物上包层。采用本发明可以制备长度满足任何芯片间光互联要求的光波导,且工艺简单,成本低。

Figure 201010117909

The invention discloses a method for preparing a polysiloxane optical waveguide for optical interconnection, and aims to provide a method for preparing an optical waveguide for optical interconnection with a length greater than 20 cm and low cost. The technical solution is to design an optical waveguide pattern and make a template; apply polyvinylidene fluoride solution on the template, and release the mold to obtain a replica; fill the grooves in the replica with a mixture of phenylmethylcyclosiloxane, phenyl After the methylcyclosiloxane mixture is solidified, it becomes the core layer of the ridge waveguide; the tetrakis (trimethylsiloxy) silane mixture is coated on the replica and baked to form a tetrakis (trimethylsiloxy) base) silane film; the replica is peeled off from the tetrakis (trimethylsiloxy) silane film, and the tetrakis (trimethylsiloxy) silane film forms the lower cladding layer; the tetrakis (trimethylsiloxy) ) silane mixture is coated on the ridge waveguide, and the tetrakis (trimethylsiloxy) silane mixture is solidified to form a polymer upper cladding. By adopting the invention, the optical waveguide whose length meets the requirement of optical interconnection between any chips can be prepared, and the process is simple and the cost is low.

Figure 201010117909

Description

一种用于光互连的聚硅氧烷光波导的制备方法A preparation method of polysiloxane optical waveguide for optical interconnection

技术领域 technical field

本发明属于光电子器件的制造方法,具体涉及一种制备聚硅氧烷光波导的方法。The invention belongs to a manufacturing method of an optoelectronic device, in particular to a method for preparing a polysiloxane optical waveguide.

背景技术 Background technique

由于计算机在超并行、大容量的数据和图像的快速计算和实时处理中存在“电子瓶颈”,光互连代替传统电互连成为了研究的热点。尤其在芯片光互连中,聚合物波导以其低成本、简单工艺、能大规模生产和集成度高的优势,在光电印制电路板中得到了广泛的应用。寻求低损耗以及用于芯片间光互连的波导材料和相应的制造工艺一直为人们所关心。Due to the "electronic bottleneck" in the fast calculation and real-time processing of super-parallel, large-capacity data and images, optical interconnection instead of traditional electrical interconnection has become a research hotspot. Especially in the optical interconnection of chips, polymer waveguides have been widely used in optoelectronic printed circuit boards due to their advantages of low cost, simple process, large-scale production and high integration. Seeking low loss and waveguide materials and corresponding manufacturing processes for optical interconnection between chips has always been concerned by people.

传统的光集成和光电集成是做在铌酸锂(LiNbO3)和硅基半导体材料上的。近年来,人们开始关注有机聚合物光波导材料的开发研究。与传统的无机光波导材料相比,有机聚合物光波导材料具有较高的电光耦合系数、较低的介电常数、较小的响应时间和较小的热损耗等特点。而且,用聚合物材料制作光波导还有这些优点:制作高质量的聚合物波导材料相对容易,同时波导材料的折射率易于调整;器件制作工艺简单,并与传统的半导体工艺相容,有利于大规模的生产,成本低。材料制作在许多类型的基底上,有利于与其它的光电子器件集成。材料种类多,因而可选择传输损耗低、价格低廉的材料来制作器件。Traditional optical integration and optoelectronic integration are done on lithium niobate (LiNbO 3 ) and silicon-based semiconductor materials. In recent years, people have begun to pay attention to the development and research of organic polymer optical waveguide materials. Compared with traditional inorganic optical waveguide materials, organic polymer optical waveguide materials have the characteristics of higher electro-optical coupling coefficient, lower dielectric constant, shorter response time and smaller heat loss. Moreover, making optical waveguides with polymer materials has these advantages: it is relatively easy to make high-quality polymer waveguide materials, and the refractive index of waveguide materials is easy to adjust; the device manufacturing process is simple and compatible with traditional semiconductor processes, which is conducive to Large-scale production, low cost. The material is fabricated on many types of substrates, facilitating integration with other optoelectronic devices. There are many kinds of materials, so materials with low transmission loss and low price can be selected to make devices.

光电集成器件的熔结温度一般在260℃,PCB版层压工艺集成器件需承受的温度不低于180℃。另一方面,在使用过程中也要求材料有一定的热稳定性。目前部分用于光波导制备研究的有机聚合物(如聚甲基丙烯酸甲酯、聚苯乙烯等)玻璃化温度低和热稳定性差,不适宜用作芯片间光互连。为满足以上需求,材料的选择上必须选取玻璃化温度高、热稳定性好的有机聚合物。聚硅氧烷(PDMS)和聚酞亚胺(PI)及其衍生物具有这方面的良好特性。The sintering temperature of optoelectronic integrated devices is generally 260°C, and the temperature that integrated devices must withstand in the PCB board lamination process is not lower than 180°C. On the other hand, the material is also required to have certain thermal stability during use. At present, some organic polymers (such as polymethyl methacrylate, polystyrene, etc.) used in the preparation of optical waveguides have low glass transition temperature and poor thermal stability, so they are not suitable for optical interconnection between chips. In order to meet the above requirements, the selection of materials must select organic polymers with high glass transition temperature and good thermal stability. Polysiloxane (PDMS) and polyimide (PI) and their derivatives have good properties in this regard.

在制备工艺方面,传统的聚合物波导制备工艺是基于传统的半导体制备工艺。首先用旋涂法在基底上制备聚合物薄膜,所需的微图形通过传统的光刻技术转移到金属保护膜上,光刻完毕后就进行ICP刻蚀。在ICP刻蚀中受光刻胶保护留下的的金属微图形膜被用作掩膜层,未被保护的聚合物在等离子体的轰击下去掉,形成所需要的聚合物微结构层,再采用腐蚀剂将金属微图形膜腐蚀掉,剩下的具有微图形结构的聚合物即成为波导材料的芯层。最后在制作好的波导芯层上旋涂聚合物上包层,加热处理使上包层固化,就形成了光波导层。In terms of preparation process, the traditional polymer waveguide preparation process is based on the traditional semiconductor preparation process. First, the polymer film is prepared on the substrate by spin coating, and the required micropattern is transferred to the metal protective film by traditional photolithography technology, and ICP etching is carried out after the photolithography is completed. In ICP etching, the metal micropattern film protected by photoresist is used as a mask layer, and the unprotected polymer is removed under the bombardment of plasma to form the required polymer microstructure layer, and then The metal micro-pattern film is etched away with an etchant, and the remaining polymer with a micro-pattern structure becomes the core layer of the waveguide material. Finally, the polymer upper cladding layer is spin-coated on the prepared waveguide core layer, and the upper cladding layer is cured by heat treatment to form the optical waveguide layer.

上述传统的光波导制备方法工艺稳定,所制备的光波导层质量高,在大规模生产中具有较大的优势。不足之处在于:目前实验室中普遍使用的光刻机紫外光均匀区有限,刻蚀设备中离子束均匀区有限,不可能用旋涂法获得大面积均匀薄膜,因此用传统光波导制备方法制备长度大于15cm的光波导有困难,而长度大于15cm的光波导才能满足芯片间光互连的要求,因此为了制备满足芯片间光互连要求的光波导必须探索新的方法。The above-mentioned traditional optical waveguide preparation method has a stable process, and the prepared optical waveguide layer is of high quality, which has great advantages in large-scale production. The disadvantage is that the uniform area of the ultraviolet light of the lithography machine commonly used in the laboratory is limited, and the uniform area of the ion beam in the etching equipment is limited. It is impossible to obtain a large-area uniform film by the spin coating method. Therefore, the traditional optical waveguide preparation method It is difficult to prepare optical waveguides with a length greater than 15 cm, and optical waveguides with a length greater than 15 cm can meet the requirements of optical interconnection between chips. Therefore, new methods must be explored in order to prepare optical waveguides that meet the requirements of optical interconnection between chips.

1990年以来,人们开发了各种直写技术(Direct Writing),如微细笔直写、金刚石刀具直写、激光直写、激光微细熔覆直写等。具有代表性的方法是微细笔直写电子元器件方法。它主要是采用特殊设计的微细笔,利用工作台的CAD/CAM功能,直接将电子浆料置放于基板表面的指定位置,形成线路板或者功能元器件。关于Micropen直写布线的具体设计方法见美国专利:“Carl E,Drumheller.Inking System for Producing CircuitPatterns.US Patent4485387,1984.”;国内具有代表性的是华中科技大学的专利:“一种具备聚合物的方法及其专用直写装置,申请号200610019923.7”。该装置通过控制施压气管中气流的通断和调节气压的大小,并向微细笔的储料腔中浆料提供所需的压力来制备波导。Since 1990, people have developed various direct writing technologies (Direct Writing), such as micro pen direct writing, diamond tool direct writing, laser direct writing, laser micro cladding direct writing, etc. A representative method is the micro-pen direct writing method of electronic components. It mainly uses a specially designed micro-pen, and uses the CAD/CAM function of the workbench to directly place the electronic paste on the designated position on the surface of the substrate to form a circuit board or functional components. For the specific design method of Micropen direct-write wiring, see the US patent: "Carl E, Drumheller.Inking System for Producing Circuit Patterns.US Patent4485387, 1984." method and its special direct writing device, application number 200610019923.7". The device prepares the waveguide by controlling the on-off of the airflow in the pressurized air pipe, adjusting the size of the air pressure, and providing the required pressure to the slurry in the material storage chamber of the micro-pen.

直写技术一般具有CAD/CAM功能,无需掩膜就可实现柔性化制造,加工精度高,无污染。不足之处在于直写装置昂贵、制作成本高且生产周期长。Direct writing technology generally has CAD/CAM functions, and can realize flexible manufacturing without masks, with high processing accuracy and no pollution. The disadvantage is that the direct writing device is expensive, the production cost is high and the production cycle is long.

发明内容 Contents of the invention

本发明要解决的技术问题是提供一种用于光互连的聚硅氧烷光波导的制备方法,采用该方法可制备长度大于20cm,且成本低、工艺简单、易于操作。The technical problem to be solved by the present invention is to provide a method for preparing a polysiloxane optical waveguide used for optical interconnection. The method can be used to prepare a polysiloxane optical waveguide with a length greater than 20 cm, and has low cost, simple process and easy operation.

本发明的技术方案是:Technical scheme of the present invention is:

第一步,采用计算机辅助设计工具设计横截面与多模光纤的芯径相匹配、长度满足芯片间光互联要求的光波导图样,将光波导图样提交给专业制版公司制得模板。The first step is to use computer-aided design tools to design an optical waveguide pattern whose cross-section matches the core diameter of the multimode fiber and whose length meets the requirements for optical interconnection between chips, and submit the optical waveguide pattern to a professional plate-making company to make a template.

第二步,将聚偏二氟乙烯溶解于二甲乙醯胺溶剂中,聚偏二氟乙烯粉末与二甲乙醯胺溶剂的质量比为1∶8。室温下混合搅拌,然后将温度升至50℃回流半小时,可得到半透明状的聚偏二氟乙烯溶液。In the second step, polyvinylidene fluoride is dissolved in dimethylacetamide solvent, and the mass ratio of polyvinylidene fluoride powder to dimethylacetamide solvent is 1:8. Mix and stir at room temperature, then raise the temperature to 50°C and reflux for half an hour to obtain a translucent polyvinylidene fluoride solution.

第三步,将聚偏二氟乙烯溶液涂覆在已制备好的模版上,控制聚偏二氟乙烯溶液的厚度为1~1.5mm。在室温下让聚偏二氟乙烯溶液中的二甲乙醯胺溶剂充分挥发,固化后的聚偏二氟乙烯薄膜从模版上脱模即得到模板的翻版。翻版中有凹槽,将在下一步中用来制作波导的芯层。In the third step, the polyvinylidene fluoride solution is coated on the prepared template, and the thickness of the polyvinylidene fluoride solution is controlled to be 1-1.5 mm. Let the dimethylacetamide solvent in the polyvinylidene fluoride solution fully volatilize at room temperature, and release the cured polyvinylidene fluoride film from the template to obtain a replica of the template. The replica has grooves in it which will be used in the next step to make the core of the waveguide.

第四步,把苯基甲基环硅氧烷溶液与其配套固化剂溶液按质量比1∶1的比例混合,得到粘度为4,000mPa·s,折射率为1.543的苯基甲基环硅氧烷混合液。用苯基甲基环硅氧烷混合液填充翻版中的凹槽,在100℃~105℃温度下烘烤一小时,苯基甲基环硅氧烷混合液固化后成为脊型波导的芯层。The fourth step is to mix the phenylmethylcyclosiloxane solution with its supporting curing agent solution in a mass ratio of 1:1 to obtain a phenylmethylcyclosiloxane with a viscosity of 4,000mPa s and a refractive index of 1.543. Mixture. Fill the grooves in the replica with phenylmethylcyclosiloxane mixture, bake at 100°C to 105°C for one hour, and the phenylmethylcyclosiloxane mixture will become the core layer of the ridge waveguide after solidification .

第五步,把四(三甲基甲硅烷氧基)硅烷溶液与其配套固化剂溶液按质量比10∶1的比例混合,得到粘度为4,000mPa·s,折射率为1.41的四(三甲基甲硅烷氧基)硅烷混合液。四(三甲基甲硅烷氧基)硅烷混合液放在密闭容器中抽真空,再用超声波振荡以去除四(三甲基甲硅烷氧基)硅烷混合液中的气泡。用流涎法把四(三甲基甲硅烷氧基)硅烷混合液涂覆在填充了苯基甲基环硅氧烷混合液的翻版上,将四(三甲基甲硅烷氧基)硅烷和翻版一起在80℃~90℃温度下烘烤一小时,使四(三甲基甲硅烷氧基)硅烷混合液发生交联反应固化,形成四(三甲基甲硅烷氧基)硅烷薄膜。The fifth step is to mix the tetrakis (trimethylsiloxy) silane solution with its supporting curing agent solution in a mass ratio of 10:1 to obtain a tetrakis (trimethylsiloxy) silane with a viscosity of 4,000 mPa s and a refractive index of 1.41. Silyloxy) silane mixture. The tetrakis(trimethylsiloxy)silane mixed solution is placed in a closed container to evacuate, and then ultrasonic vibration is used to remove the air bubbles in the tetrakis(trimethylsiloxy)silane mixed solution. Coat tetrakis (trimethylsiloxy) silane mixed solution on the replica filled with phenylmethylcyclosiloxane mixed solution by salivation method, tetrakis (trimethylsiloxy) silane and replica Baking together at a temperature of 80° C. to 90° C. for one hour allows the tetrakis(trimethylsiloxy)silane mixture to undergo a cross-linking reaction and solidify to form a tetrakis(trimethylsiloxy)silane film.

第六步,将翻版从四(三甲基甲硅烷氧基)硅烷薄膜上剥离,四(三甲基甲硅烷氧基)硅烷薄膜形成下包层,留在四(三甲基甲硅烷氧基)硅烷薄膜上的苯基甲基环硅氧烷形成芯层。对于下包层和芯层上可能残留的聚偏二氟乙烯可用丙酮溶去,初步形成以空气为上包层的脊形波导。In the sixth step, the replica is peeled off from the tetrakis (trimethylsiloxy) silane film, and the tetrakis (trimethylsiloxy) silane film forms the lower cladding layer, leaving the tetrakis (trimethylsiloxy) ) phenylmethylcyclosiloxane on a silane film to form the core layer. The polyvinylidene fluoride that may remain on the lower cladding and core layer can be dissolved with acetone, and a ridge waveguide with air as the upper cladding is initially formed.

第七步,将四(三甲基甲硅烷氧基)硅烷混合液涂覆在第六步制备的以空气为上包层的脊形波导上,四(三甲基甲硅烷氧基)硅烷混合液固化,形成聚合物上包层。得到以苯基甲基环硅氧烷为芯层,四(三甲基甲硅烷氧基)硅烷为上包层和下包层的脊型波导。In the seventh step, the tetrakis (trimethylsiloxy) silane mixture is coated on the ridge waveguide with air as the upper cladding prepared in the sixth step, and the tetrakis (trimethylsiloxy) silane is mixed The liquid solidifies to form a polymer overcladding. A ridge-shaped waveguide with phenylmethylcyclosiloxane as the core layer and tetrakis(trimethylsiloxy)silane as the upper and lower cladding layers is obtained.

采用本发明可以达到以下技术效果:Adopt the present invention can reach following technical effect:

1.由于本发明第一步设计的光波导图样的长度满足芯片间光互联要求,模板的制备是成熟技术,长度根据光波导图样的长度制得,因此采用本发明能制备长度满足任何芯片间光互联要求的光波导,使得制备长度大于20cm的光波导变得很容易。1. Since the length of the optical waveguide pattern designed in the first step of the present invention meets the requirements for optical interconnection between chips, the preparation of the template is a mature technology, and the length is obtained according to the length of the optical waveguide pattern, so the present invention can be used to prepare the length to meet the requirements of any inter-chip The optical waveguide required for optical interconnection makes it easy to prepare an optical waveguide with a length greater than 20 cm.

2.因为用作芯层的苯基甲基环硅氧烷和包层的四(三甲基甲硅烷氧基)硅烷玻璃化温度高、热稳定性好,所以本发明制备的光波导可用于基于层压工艺的PCB板上的光互连。2. Because the phenylmethylcyclosiloxane used as the core layer and the tetrakis (trimethylsiloxy) silane of the cladding have a high glass transition temperature and good thermal stability, the optical waveguide prepared by the present invention can be used for Optical interconnection on PCB board based on lamination process.

3.由于采用本发明制备光波导时芯层和上下包层的材料均为聚硅氧烷,所以制备出的光波导传输损耗低,低于0.14dB/cm。3. Since the materials of the core layer and the upper and lower cladding layers are polysiloxane when the optical waveguide is prepared by the present invention, the transmission loss of the prepared optical waveguide is low, lower than 0.14dB/cm.

4.本发明工艺简单,易于操作。4. The process of the present invention is simple and easy to operate.

附图说明 Description of drawings

图1为本发明的总体流程图;Fig. 1 is the general flowchart of the present invention;

图2是采用本发明制备光波导时光波导各组件的变化示意图。Fig. 2 is a schematic view showing the changes of components of the optical waveguide prepared by the present invention.

具体实施方式 Detailed ways

图1是本发明的总体流程图,图2是采用本发明制备光波导时光波导各组件的变化示意图。Fig. 1 is an overall flow chart of the present invention, and Fig. 2 is a schematic view showing changes of components of the optical waveguide prepared by the present invention.

如图2(a)-(e)所示,本发明的步骤为:As shown in Figure 2 (a)-(e), the steps of the present invention are:

(1)采用计算机辅助设计工具设计横截面与多模光纤的芯径相匹配、长度满足芯片间光互联要求的光波导图样,将光波导图样提交给专业制版公司制得模板1,如图2(a)所示。(1) Use computer-aided design tools to design an optical waveguide pattern whose cross-section matches the core diameter of the multimode fiber and whose length meets the requirements for optical interconnection between chips, and submit the optical waveguide pattern to a professional plate-making company to make template 1, as shown in Figure 2 (a) shown.

(2)将聚偏二氟乙烯即聚偏二氟乙烯粉末溶解于二甲乙醯胺二甲乙醯胺溶剂中,两者的质量比为1∶8。室温下混合搅拌,然后将温度升至50℃回流半小时,得到半透明状的聚偏二氟乙烯溶液。(2) Dissolving polyvinylidene fluoride, that is, polyvinylidene fluoride powder, in dimethylacetamide dimethylacetamide solvent, the mass ratio of the two is 1:8. Mix and stir at room temperature, then raise the temperature to 50° C. and reflux for half an hour to obtain a translucent polyvinylidene fluoride solution.

(3)用聚偏二氟乙烯溶液涂覆在模版1上,控制聚偏二氟乙烯溶液的厚度为1~1.5mm。在室温下让聚偏二氟乙烯溶液中的二甲乙醯胺溶剂充分挥发,固化后聚偏二氟乙烯薄膜脱模即得到模板1的翻版2,如图2(b)所示。(3) Coating the template 1 with a polyvinylidene fluoride solution, controlling the thickness of the polyvinylidene fluoride solution to be 1-1.5 mm. The dimethylacetamide solvent in the polyvinylidene fluoride solution was allowed to fully evaporate at room temperature, and after curing, the polyvinylidene fluoride film was released from the mold to obtain the replica 2 of the template 1, as shown in Figure 2(b).

(4)把苯基甲基环硅氧烷溶液与其配套固化剂溶液按质量比1∶1的比例混合,得到苯基甲基环硅氧烷混合液,用苯基甲基环硅氧烷混合液填充翻版2中的凹槽,在100℃~105℃温度下烘烤一小时,苯基甲基环硅氧烷混合液固化后得到的芯层3,如图2(c)所示。(4) Mix the phenylmethylcyclosiloxane solution with its supporting curing agent solution in a mass ratio of 1:1 to obtain a phenylmethylcyclosiloxane mixture, which is mixed with phenylmethylcyclosiloxane Fill the grooves in replica 2 with liquid, bake at 100° C. to 105° C. for one hour, and obtain the core layer 3 after curing the phenylmethylcyclosiloxane mixture, as shown in FIG. 2( c ).

(5)把四(三甲基甲硅烷氧基)硅烷溶液与其配套固化剂溶液按质量比10∶1的比例混合,得到四(三甲基甲硅烷氧基)硅烷混合液。四(三甲基甲硅烷氧基)硅烷混合液放在密闭容器中抽真空,再用超声波振荡以去除四(三甲基甲硅烷氧基)硅烷混合液中的气泡。用流涎法把四(三甲基甲硅烷氧基)硅烷混合液涂覆在填充了芯层3的翻版2上,将四(三甲基甲硅烷氧基)硅烷和翻版2一起在80℃~90℃烘烤一小时,使四(三甲基甲硅烷氧基)硅烷混合液发生交联反应固化,形成四(三甲基甲硅烷氧基)硅烷薄膜4,如图2(d)所示。(5) Mix the tetrakis(trimethylsiloxy)silane solution with its supporting curing agent solution at a mass ratio of 10:1 to obtain a tetrakis(trimethylsiloxy)silane mixed solution. The tetrakis(trimethylsiloxy)silane mixed solution is placed in a closed container to evacuate, and then ultrasonic vibration is used to remove the air bubbles in the tetrakis(trimethylsiloxy)silane mixed solution. Coat tetrakis (trimethylsiloxy) silane mixed solution on replica 2 filled with core layer 3 by salivation method, put tetrakis (trimethylsiloxy) silane and replica 2 together at 80℃~ Bake at 90°C for one hour to allow the tetrakis(trimethylsiloxy)silane mixture to undergo a crosslinking reaction and solidify to form a tetrakis(trimethylsiloxy)silane film 4, as shown in Figure 2(d) .

(6)将翻版2从四(三甲基甲硅烷氧基)硅烷薄膜4上剥离,四(三甲基甲硅烷氧基)硅烷薄膜4形成下包层5,留在四(三甲基甲硅烷氧基)硅烷薄膜4上的苯基甲基环硅氧烷形成芯层3,如图2(e)所示。对于下包层5和芯层3上可能残留的聚偏二氟乙烯可用丙酮溶去,初步形成以空气为上包层的脊形波导。(6) The replica 2 is peeled off from the tetrakis (trimethylsiloxy) silane film 4, and the tetrakis (trimethylsiloxy) silane film 4 forms the lower cladding layer 5, leaving the tetrakis (trimethylsiloxy) silane film The phenylmethylcyclosiloxane on the siloxy)silane film 4 forms the core layer 3, as shown in FIG. 2(e). The polyvinylidene fluoride that may remain on the lower cladding layer 5 and the core layer 3 can be dissolved with acetone to initially form a ridge waveguide with air as the upper cladding layer.

(7)将四(三甲基甲硅烷氧基)硅烷混合液涂覆在第(6)步制备的以空气为上包层的脊形波导上,固化形成聚合物上包层6,如图2(f)所示。得到苯基甲基环硅氧烷为芯层3,四(三甲基甲硅烷氧基)硅烷为上包层6、下包层5的脊型波导。(7) Coat the mixed solution of tetrakis(trimethylsiloxy)silane on the ridge waveguide with air as the upper cladding prepared in step (6), and solidify to form the polymer upper cladding 6, as shown in the figure 2(f). A ridge waveguide in which phenylmethylcyclosiloxane is used as the core layer 3 , tetrakis(trimethylsiloxy)silane is used as the upper cladding layer 6 and the lower cladding layer 5 is obtained.

Claims (5)

1.一种用于光互连的聚硅氧烷光波导的制备方法,其特征在于包括以下步骤:1. A preparation method for a polysiloxane optical waveguide for optical interconnection, characterized in that it may further comprise the steps: 第一步,采用计算机辅助设计工具设计横截面与多模光纤的芯径相匹配、长度满足芯片间光互联要求的光波导图样,将光波导图样提交给专业制版公司制得模板;The first step is to use computer-aided design tools to design an optical waveguide pattern whose cross-section matches the core diameter of the multimode fiber and whose length meets the requirements for optical interconnection between chips, and submit the optical waveguide pattern to a professional plate-making company to make a template; 第二步,将聚偏二氟乙烯粉末溶解于二甲乙醯胺溶剂中,聚偏二氟乙烯粉末与二甲乙醯胺溶剂的质量比为1∶8,室温下混合搅拌,然后将温度升至50℃回流半小时,得到半透明状的聚偏二氟乙烯溶液;In the second step, polyvinylidene fluoride powder is dissolved in dimethylacetamide solvent, the mass ratio of polyvinylidene fluoride powder and dimethylacetamide solvent is 1:8, mixing and stirring at room temperature, and then the temperature is raised to Reflux at 50°C for half an hour to obtain a translucent polyvinylidene fluoride solution; 第三步,将聚偏二氟乙烯溶液涂覆在已制备好的模版(1)上,在室温下让聚偏二氟乙烯溶液中的二甲乙醯胺溶剂充分挥发,固化后的聚偏二氟乙烯薄膜从模版(1)上脱模即得到模板的翻版(2);In the third step, the polyvinylidene fluoride solution is coated on the prepared template (1), and the dimethylacetamide solvent in the polyvinylidene fluoride solution is fully volatilized at room temperature, and the cured polyvinylidene difluoride The vinyl fluoride film is released from the template (1) to obtain a replica of the template (2); 第四步,把苯基甲基环硅氧烷溶液与其配套固化剂溶液按质量比1∶1的比例混合,得到苯基甲基环硅氧烷混合液;用苯基甲基环硅氧烷混合液填充翻版(2)中的凹槽,在100℃~105℃温度下烘烤一小时,苯基甲基环硅氧烷混合液固化后成为脊型波导的芯层(3);The fourth step is to mix the phenylmethylcyclosiloxane solution with its supporting curing agent solution in a mass ratio of 1:1 to obtain a phenylmethylcyclosiloxane mixture; use the phenylmethylcyclosiloxane The mixed liquid fills the grooves in the replica (2), and is baked at a temperature of 100° C. to 105° C. for one hour, and the phenylmethylcyclosiloxane mixed liquid becomes the core layer (3) of the ridge waveguide after curing; 第五步,把四(三甲基甲硅烷氧基)硅烷溶液与其配套固化剂溶液按质量比10∶1的比例混合,得到四(三甲基甲硅烷氧基)硅烷混合液;四(三甲基甲硅烷氧基)硅烷混合液放在密闭容器中抽真空,再用超声波振荡以去除四(三甲基甲硅烷氧基)硅烷混合液中的气泡;用流涎法把四(三甲基甲硅烷氧基)硅烷混合液涂覆在填充了苯基甲基环硅氧烷混合液的翻版(2)上,将四(三甲基甲硅烷氧基)硅烷和翻版(2)一起在80℃~90℃温度下烘烤一小时,使四(三甲基甲硅烷氧基)硅烷混合液发生交联反应固化,形成四(三甲基甲硅烷氧基)硅烷薄膜(4);The fifth step is to mix the tetrakis (trimethylsiloxy) silane solution with its supporting curing agent solution in a mass ratio of 10:1 to obtain a tetrakis (trimethylsiloxy) silane mixed solution; Methylsiloxy) silane mixture is placed in a closed container to evacuate, and then ultrasonic vibration is used to remove the bubbles in the tetrakis (trimethylsiloxy) silane mixture; The silyloxy) silane mixed solution is coated on the replica (2) filled with the phenylmethylcyclosiloxane mixed solution, and the tetrakis (trimethylsiloxy) silane and the replica (2) are heated together at 80 Bake for one hour at a temperature of °C to 90°C to cause the tetrakis(trimethylsiloxy)silane mixture to undergo a crosslinking reaction and solidify to form a tetrakis(trimethylsiloxy)silane film (4); 第六步,将翻版(2)从四(三甲基甲硅烷氧基)硅烷薄膜(4)上剥离,四(三甲基甲硅烷氧基)硅烷薄膜(4)形成下包层(5),留在四(三甲基甲硅烷氧基)硅烷薄膜(4)上的苯基甲基环硅氧烷形成芯层(3),初步形成以空气为上包层的脊形波导;In the sixth step, the replica (2) is peeled off from the tetrakis (trimethylsiloxy) silane film (4), and the tetrakis (trimethylsiloxy) silane film (4) forms the lower cladding layer (5) , the phenylmethyl cyclosiloxane left on the tetrakis (trimethylsiloxy) silane film (4) forms a core layer (3), and initially forms a ridge waveguide with air as the upper cladding; 第七步,将四(三甲基甲硅烷氧基)硅烷混合液涂覆在第六步制备的以空气为上包层的脊形波导上,四(三甲基甲硅烷氧基)硅烷混合液固化,形成聚合物上包层(6),得到以苯基甲基环硅氧烷为芯层(3),四(三甲基甲硅烷氧基)硅烷为上包层(6)和下包层(5)的脊型波导。In the seventh step, the tetrakis (trimethylsiloxy) silane mixture is coated on the ridge waveguide with air as the upper cladding prepared in the sixth step, and the tetrakis (trimethylsiloxy) silane is mixed The liquid is solidified to form an upper cladding layer (6) of the polymer, and obtain a core layer (3) with phenylmethylcyclosiloxane, tetrakis (trimethylsiloxy) silane as an upper cladding layer (6) and a lower cladding layer (6). Ridge waveguide with cladding (5). 2.如权利要求1所述的一种用于光互连的聚硅氧烷光波导的制备方法,其特征在于将聚偏二氟乙烯溶液涂覆在已制备好的模版(1)上时控制聚偏二氟乙烯溶液的厚度为1~1.5mm。2. a kind of preparation method for the polysiloxane optical waveguide that is used for optical interconnection as claimed in claim 1, it is characterized in that when polyvinylidene fluoride solution is coated on the template (1) that has prepared Control the thickness of the polyvinylidene fluoride solution to be 1-1.5mm. 3.如权利要求1所述的一种用于光互连的聚硅氧烷光波导的制备方法,其特征在于所述苯基甲基环硅氧烷混合液粘度为4,000mPa·s,折射率为1.543。3. a kind of preparation method for the polysiloxane optical waveguide that is used for optical interconnection as claimed in claim 1, it is characterized in that the viscosity of described phenylmethylcyclosiloxane mixed liquid is 4,000mPa·s, refraction The rate is 1.543. 4.如权利要求1所述的一种用于光互连的聚硅氧烷光波导的制备方法,其特征在于所述四(三甲基甲硅烷氧基)硅烷混合液粘度为4,000mPa·s,折射率为1.41。4. a kind of preparation method for the polysiloxane optical waveguide that is used for optical interconnection as claimed in claim 1, is characterized in that described tetrakis (trimethylsiloxy) silane mixed solution viscosity is 4,000mPa. s, the refractive index is 1.41. 5.如权利要求1所述的一种用于光互连的聚硅氧烷光波导的制备方法,其特征在于第六步所述下包层(5)和芯层(3)上可能残留的聚偏二氟乙烯用丙酮溶去。5. a kind of preparation method for the polysiloxane optical waveguide that is used for optical interconnection as claimed in claim 1, it is characterized in that possibly residual The polyvinylidene fluoride was dissolved in acetone.
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