JPS60208711A - Optical coupler - Google Patents

Optical coupler

Info

Publication number
JPS60208711A
JPS60208711A JP6485784A JP6485784A JPS60208711A JP S60208711 A JPS60208711 A JP S60208711A JP 6485784 A JP6485784 A JP 6485784A JP 6485784 A JP6485784 A JP 6485784A JP S60208711 A JPS60208711 A JP S60208711A
Authority
JP
Japan
Prior art keywords
film
grating
photopolymerizable
substrate
monomolecular
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
Application number
JP6485784A
Other languages
Japanese (ja)
Inventor
Yukio Nishimura
征生 西村
Mamoru Miyawaki
守 宮脇
Tetsushi Nose
哲志 野瀬
Takashi Nakagiri
孝志 中桐
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Canon Inc
Original Assignee
Canon Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Canon Inc filed Critical Canon Inc
Priority to JP6485784A priority Critical patent/JPS60208711A/en
Publication of JPS60208711A publication Critical patent/JPS60208711A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/24Coupling light guides
    • G02B6/26Optical coupling means
    • G02B6/28Optical coupling means having data bus means, i.e. plural waveguides interconnected and providing an inherently bidirectional system by mixing and splitting signals
    • G02B6/293Optical coupling means having data bus means, i.e. plural waveguides interconnected and providing an inherently bidirectional system by mixing and splitting signals with wavelength selective means
    • G02B6/29304Optical coupling means having data bus means, i.e. plural waveguides interconnected and providing an inherently bidirectional system by mixing and splitting signals with wavelength selective means operating by diffraction, e.g. grating
    • G02B6/29316Light guides comprising a diffractive element, e.g. grating in or on the light guide such that diffracted light is confined in the light guide
    • G02B6/29325Light guides comprising a diffractive element, e.g. grating in or on the light guide such that diffracted light is confined in the light guide of the slab or planar or plate like form, i.e. confinement in a single transverse dimension only
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/10Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type
    • G02B6/12Light 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
    • G02B6/13Integrated optical circuits characterised by the manufacturing method

Abstract

PURPOSE:To improve performance and to reduce cost by constituting an optical waveguide installed with a grating of an accumulated monomolecular film of a photopolymerizable olefin compd. so that sharp-edged microshapes are easily formed. CONSTITUTION:The accumulated monomolecular film 10 (hereunder abbreviated as LB film) is formed on a substrate 2 by Langmuir-Projet method (hereunder abbreviated as LB method) using a photopolymerizable monomer (e.g.; formula I , formula II) having a hydrophilic group, hydrophobic group and at least one unsatd. bond in the molecule. After the LB film 10 is patterned and exposed, the unexposed part is dissolved away by developing the film to build a lower part 12 of a waveguide consisting of the polymerized LB film. The polymerizable LB film 13 is formed by the LB method on the part 12 and the film 13 is exposed to a grating pattern by an energy ray 11, then the unexeposed part is dissolved away by developing the film, by which the intended grating type optical coupler is obtd.

Description

【発明の詳細な説明】 本発明は光重合性化合物からなる光結合器、さらに詳し
くは、光重合性オレフィン系化合物の重合単分子累積膜
からなるグレーティング構造を有する光結合器に関する
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an optical coupler made of a photopolymerizable compound, and more particularly to an optical coupler having a grating structure made of a polymerized monomolecular cumulative film of a photopolymerizable olefin compound.

近年、光集積回路の発達に伴って高精度で、かつ効率の
良い光結合器が望まれている。
In recent years, with the development of optical integrated circuits, there has been a demand for highly accurate and efficient optical couplers.

しかしながら、従来、所望の精度の結合器を得るために
は高度の微細加工技術を必要とするため、いきおい歩留
りの低下、したがってコスト高を招(といった欠陥があ
った。
However, in the past, in order to obtain a coupler with the desired precision, advanced microfabrication techniques were required, which resulted in lower yields and higher costs.

ここでのグレーティング型光結合器について説明する。The grating type optical coupler here will be explained.

第1図はグレーティング型光結合器の断面図で、この図
において2は基板であって、例えば、ガラス、プラスチ
ック又はニオブ酸リチウム(LiNbOs )等の透明
基板又はシリコン、セラミックス等の不透明基板が用い
られる。基板2の表面に光導波路1が配設される。光導
波路lは基板2よりも屈折率が高いものが用いられる。
FIG. 1 is a cross-sectional view of a grating type optical coupler. In this figure, 2 is a substrate, for example, a transparent substrate such as glass, plastic or lithium niobate (LiNbOs), or an opaque substrate such as silicon or ceramics. It will be done. An optical waveguide 1 is arranged on the surface of a substrate 2. The optical waveguide l has a higher refractive index than the substrate 2.

例えば、−オプ酸すテクムを基板として用いる場合には
、その表面にチタン(Ti)を熱拡散することによって
0.5〜5μ程度の膜厚の光導波路1が得られる。
For example, in the case of using -optic acid TECHUM as a substrate, the optical waveguide 1 having a film thickness of about 0.5 to 5 .mu.m can be obtained by thermally diffusing titanium (Ti) onto its surface.

或いは、屈折率が1.5のガラスを基板として用いる場
合には、その表面に屈折率が1.55(波長6828A
)のガラス(例えば、コーニング社商品名C−7059
)をスパッタリングにより膜厚0.5〜5μ程度に成膜
し、光導波路lを得る。
Alternatively, if glass with a refractive index of 1.5 is used as a substrate, the surface of the glass has a refractive index of 1.55 (wavelength 6828A).
) glass (for example, Corning C-7059)
) is formed into a film with a thickness of about 0.5 to 5 μm by sputtering to obtain an optical waveguide l.

6はグレーティングで、通常ピッチ0.8〜1μ深さ0
.1〜0.2μである。このように構成された光結合器
に入射光8が入ると、導波路内を光4が全反射により伝
播し、グレーティング6によって回折され射出光5がと
り出される。
6 is a grating, usually pitch 0.8~1μ depth 0
.. It is 1 to 0.2μ. When the incident light 8 enters the optical coupler configured in this way, the light 4 propagates through the waveguide by total reflection, is diffracted by the grating 6, and the emitted light 5 is taken out.

この場合、一般にグレーティングの製作が困難である。In this case, it is generally difficult to manufacture the grating.

グレーティング6の機能をより効果的に発揮するために
は完全に矩形のグレーティングが好ましいが、そのよう
な完全矩形のグレーティングを得ることは一般に困難で
あるからである。
In order to more effectively exhibit the function of the grating 6, a completely rectangular grating is preferable, but it is generally difficult to obtain such a completely rectangular grating.

従来より光重合性有機化合物を薄膜にして用いるグレー
ティング構造を有する光結合器が知られている。
2. Description of the Related Art Optical couplers having a grating structure using a photopolymerizable organic compound in the form of a thin film have been known.

その製作方法は、まず光重合性有機化合物の溶液を回転
塗布機などを用いて、ガラス、プラスチック、半導体、
誘電体等の基板上に塗布し薄膜を形成する。次に、マス
キングして紫外線等を照射し選択的に重合させ、未露光
部分を除去してグレーティング等を作り、光結合器とし
て使用される。
The manufacturing method is to first apply a solution of a photopolymerizable organic compound to glass, plastic, semiconductors, etc. using a spin coating machine.
It is applied onto a substrate such as a dielectric material to form a thin film. Next, it is masked and irradiated with ultraviolet rays to selectively polymerize, and the unexposed portions are removed to create a grating or the like, which is used as an optical coupler.

しかしながら、該かる従来法では、薄膜の分子配向がラ
ンダムであるため微視的にみた場合、次のような弊害が
生ずる。即ち、どんなに解像力の良い光重合性有機化合
物を用いても、微小領域では鋭いエッヂを得ることがで
きず、そのため光集積回路の製作に不可欠な高性能の光
結合器が得られないと云う欠点があった。
However, in this conventional method, since the molecular orientation of the thin film is random, when viewed microscopically, the following disadvantages occur. In other words, no matter how good the resolution of a photopolymerizable organic compound is, it is not possible to obtain sharp edges in a microscopic area, and as a result, a high-performance optical coupler, which is essential for the production of optical integrated circuits, cannot be obtained. was there.

本発明は、上記に鑑みてなされたもので、微小化容易で
高性能の光結合器を提供することを目的とする。また、
本発明の目的は、分子内に親水基。
The present invention has been made in view of the above, and an object of the present invention is to provide a high-performance optical coupler that is easy to miniaturize. Also,
The object of the present invention is to provide hydrophilic groups within the molecule.

疎水基および少なくとも1個の不飽和結合を有する光重
合性上ツマ−特に光重合性オレフィン化合物からなる光
記録媒体用化合物の使用により達成される。
This is achieved by using a compound for optical recording media consisting of a photopolymerizable polymer having a hydrophobic group and at least one unsaturated bond, especially a photopolymerizable olefin compound.

本発明の光重合性上ツマ−は、基板上に単分子膜または
単分子層累積膜を形成し得る。基板上に形成された単分
子層累積膜に光を照射して照射部位において重合反応を
生じさせ、非照射部位の未重合部分を現像除去して光結
合器を形成する。
The photopolymerizable layer of the present invention can form a monomolecular film or a monomolecular layer stack on a substrate. A monomolecular layer cumulative film formed on a substrate is irradiated with light to cause a polymerization reaction in the irradiated areas, and unpolymerized portions in non-irradiated areas are removed by development to form an optical coupler.

本発明に使用する光重合性上ツマ−としては、分子内に
親水基、疎水基および少なくとも1個の不飽和結合を有
する光重合性上ツマ−であれば広く使うことができる。
As the photopolymerizable polymer used in the present invention, a wide variety of photopolymerizable polymers can be used as long as they have a hydrophilic group, a hydrophobic group, and at least one unsaturated bond in the molecule.

この様な光重合性上ツマ−は、一般式(I[a) 。Such a photopolymerizable polymer has the general formula (I[a).

(nb )で表わすことができる。(nb).

R,−CH=CH−R1(II a )R,−CH=C
H−R,−CH=CH−R1(nb)上式(I[a)R
+部或いは、R1及び一部に親水性部位と疎水性部位の
両者が存在するか、若しくは、Roは鳥との関係におい
て疎水性であり、R1はR,との関係において親水性で
ある。上式(nb)において、R1−R1またはR,部
のいずれかに親水性部位と疎水性部位の両者が存在する
か、若しくはRt、RtおよびR1部のいずれかが他の
部との関係において疎水性であり、残りの部のいずれか
は親水性である。特に炭素原子数10〜8oの長鎖アル
キル基をR1部或いは、爬及び4部、若しくはR1−R
1または4部の少なくともいずれかに有する光重合性上
ツマ−が望ましい。
R, -CH=CH-R1 (IIa) R, -CH=C
H-R, -CH=CH-R1 (nb) above formula (I[a)R
Either both a hydrophilic site and a hydrophobic site are present in the + part or R1 and a part, or Ro is hydrophobic in relation to the bird and R1 is hydrophilic in relation to R. In the above formula (nb), both a hydrophilic site and a hydrophobic site are present in either R1-R1 or R, or any of Rt, Rt, and R1 is present in the relationship with other parts. It is hydrophobic and any of the remaining parts are hydrophilic. In particular, a long-chain alkyl group having 10 to 8 carbon atoms can have R1 parts, or R1-R parts, or R1-R parts.
A photopolymerizable polymer containing at least 1 or 4 parts is desirable.

本発明の光重合性上ツマ−の具体的な例としては以下の
化合物が例示される。
Specific examples of the photopolymerizable polymer of the present invention include the following compounds.

53− 前記の光重合性上ツマ−は、長鎖アルキル基を新たに導
入した点を除けば、それ自体公知(文献衣;化学と工業
第82巻第10号768〜765頁)であるか、又は、
それに類似した構造を持つ化合物である。故に公知の方
法により合成することができる。例えば、炭素原子数1
8の長鎖アルキル基(n−オクタデカノイル基)を有す
る光重合性オンフィンモノマーである過塩素酸1.4−
ジ−n−オクタデカノイル−2,5−ジスチリルピラジ
ンAは以下の方法により合成することができる。
53- Is the above-mentioned photopolymerizable polymer known per se (References: Kagaku to Kogyo Vol. 82, No. 10, pp. 768-765), except that a long-chain alkyl group is newly introduced? , or
It is a compound with a similar structure. Therefore, it can be synthesized by a known method. For example, the number of carbon atoms is 1
Perchloric acid 1.4- is a photopolymerizable onfin monomer having 8 long-chain alkyl groups (n-octadecanoyl groups).
Di-n-octadecanoyl-2,5-distyrylpyrazine A can be synthesized by the following method.

10.8# 2.5−ジメチルピラジンと44.5gp
−クロルベンゼンスルホン酸−n−オクタデカノイルエ
ステルとを100 mJ DMFにとかし、窒素雰囲気
下にて1時間加熱還流する。冷却後、過塩素酸ナトリウ
ム10gを水200dに溶かした溶液を加える。
10.8# 2.5-dimethylpyrazine and 44.5gp
-chlorobenzenesulfonic acid-n-octadecanoyl ester was dissolved in 100 mJ DMF and heated under reflux for 1 hour under nitrogen atmosphere. After cooling, a solution of 10 g of sodium perchlorate in 200 d of water is added.

析出した固体をエーテルで洗浄した後、メチルアルコー
ル中で再結晶させる。こうして得た、過塩素酸1.4−
 n−オクタデカノイ/l/ −fj、、 5−ジメチ
ルピラジン4.7gとベンズアルデヒド1.0411と
を無水酢酸中で8時間加熱還流し、冷却後メチルアルコ
ール中で再結晶させてAを得る(収率40チ。
After washing the precipitated solid with ether, it is recrystallized in methyl alcohol. Thus obtained perchloric acid 1.4-
n-octadecanoy/l/-fj,, 4.7 g of 5-dimethylpyrazine and 1.0411 g of benzaldehyde are heated under reflux in acetic anhydride for 8 hours, and after cooling, recrystallized in methyl alcohol to obtain A (yield: 40 chi.

他の化合物もこれと同様の手法により合成することがで
きる。
Other compounds can also be synthesized by a similar method.

前記単分子膜または単分子層累積膜を作成する方法とし
ては、例えば、1.Langmuir らの開発したラ
ングミュア・プロジェット法(LB法)を用いる。ラン
グミュア・プロジェット法は、分子内に親水基と疎水基
を有する構造の分子において、両者のバランス(両親媒
性のバランス)が適度に保たれているとき、分子は水面
上で親水基を下に向けて単分子の層になることを利用し
て単分子膜または単分子層の累積膜を作成する方法であ
る。
As a method for creating the monomolecular film or monomolecular layer cumulative film, for example, 1. The Langmuir-Prodgett method (LB method) developed by Langmuir et al. is used. The Langmuir-Prodgett method uses a molecule with a structure that has a hydrophilic group and a hydrophobic group, and when the balance between the two (balance of amphiphilicity) is maintained appropriately, the molecule lowers the hydrophilic group on the water surface. This is a method of creating a monomolecular film or a cumulative film of monomolecular layers by utilizing the fact that it becomes a monomolecular layer towards the end.

水面上の単分子1は二次元系の特徴をもつ。分子がまば
らに散開しているときは、一分子当り面積Aと表面圧 
との間に二次元理想気体の式、A=KT が成り立ち、′気体膜1となる。ここに、Kはポルツマ
ン定数、Tは絶対温度である。Aを十分小さくすれば分
子間相互作用が強まり二次元固体の1凝縮膜(または固
体膜)−になる。凝縮膜はガラスなどの基板の表面へ一
層ずつ移すことかできる。この方法を用いて、単分子膜
または単分子層累積膜は例えば次のようにして製造する
A single molecule 1 on the water surface has the characteristics of a two-dimensional system. When the molecules are sparsely dispersed, the area per molecule A and the surface pressure
The two-dimensional ideal gas equation, A=KT, holds true between the two, resulting in 'gas film 1'. Here, K is Portzmann's constant and T is absolute temperature. If A is made sufficiently small, the intermolecular interaction will be strengthened, resulting in a two-dimensional solid condensation film (or solid film). The condensed film can be transferred layer by layer to the surface of a substrate such as glass. Using this method, a monomolecular film or a monomolecular layer stack is produced, for example, as follows.

まず光重合性上ツマ−を溶剤に溶解し、これを水相中に
展開し光重合性上ツマ−を膜状に析出させる。次にこの
析出物が水相上を自由に拡散して拡がりすぎないように
仕切板(または浮子)を設けて展開面積を制限して膜物
質の集合状態を制御し、その集合状態に比例した表面圧
 を得る。この仕切板を動かし、展開面積を縮少して膜
物質の集合状態を制御し、表面圧を徐々に上昇させ、累
積膜の製造に適する表面圧 を設定することができる。
First, a photopolymerizable upper layer is dissolved in a solvent, and this is spread in an aqueous phase to precipitate the photopolymerizable upper layer in the form of a film. Next, to prevent this precipitate from freely diffusing on the aqueous phase and spreading too much, a partition plate (or float) is installed to limit the area of development and control the state of aggregation of the film substance, and the Obtain the surface pressure. By moving this partition plate, the developed area can be reduced to control the state of aggregation of the membrane material, and the surface pressure can be gradually increased to set the surface pressure suitable for producing a cumulative membrane.

この表面圧を維持しながら静かに清浄な基板を垂直に上
下させることにより単分子膜が基板上に移しとられる。
The monomolecular film is transferred onto the substrate by gently vertically moving the clean substrate up and down while maintaining this surface pressure.

単分子膜は以上で製造されるが、単分子層累積膜は、前
記の操作を繰り返すことにより所望の累積度の単分子層
累積膜が形成される。このように形成した単分子膜およ
び単分子層累積膜をLB膜という。
A monomolecular layer film is produced as described above, and a monomolecular layer cumulative film having a desired degree of accumulation is formed by repeating the above-mentioned operations. The monomolecular film and monomolecular layer cumulative film thus formed are referred to as LB films.

この単分子累積膜(LB膜)にあるパターンに従ってガ
ンマ線、X線、紫外線など重合に必要なエネルギーを供
給しうる光を照射すると照射部位において■式に示すよ
うに重合がおこる。
When this monomolecular cumulative film (LB film) is irradiated with light capable of supplying the energy necessary for polymerization, such as gamma rays, X-rays, and ultraviolet rays, according to the pattern, polymerization occurs at the irradiated area as shown in equation (2).

これらの反応は互いに隣接する不飽和結合の距離が4A
以下のときおこり得るものであり、先に述べた様な方法
で作成された単分子膜又は、単分子層累積膜では、同一
層内の隣接分子間又は累積する層の隣接する分子間にお
いて可能である。また、重合した後は、暗所下でも解重
合は起こらず、非照射部位は単量体のままであるので、
現像液に溶解し所定の形状が得られる。
In these reactions, the distance between adjacent unsaturated bonds is 4A.
This can occur in the following cases, and in a monomolecular film or a monomolecular stacked film created by the method described above, it can occur between adjacent molecules in the same layer or between adjacent molecules in the cumulative layer. It is. In addition, after polymerization, depolymerization does not occur even in the dark, and the non-irradiated parts remain monomers.
It is dissolved in a developer to obtain a predetermined shape.

つぎに本発明の製作例を図面を参照して説明する。Next, a manufacturing example of the present invention will be explained with reference to the drawings.

第2図(イl 、 (C7) 、(ハ)、に)、(ホ)
)、(へ)は本発明の製作順序を示す断面図であって、
これらの図において、1、重合性LB膜10を基板2の
表面にLB法により付着形成せしめる(第2図(イ))
Figure 2 (I, (C7), (C), ni), (E)
) and (f) are sectional views showing the manufacturing order of the present invention,
In these figures, 1. A polymerizable LB film 10 is attached and formed on the surface of a substrate 2 by the LB method (Figure 2 (a)).
.

2、光等のエネルギー線11により重合性LB膜10を
バターニング露光する(第2図(ロ))。
2. The polymerizable LB film 10 is patterned and exposed to energy rays 11 such as light (FIG. 2 (b)).

8、次いで、現像(アルコール、クロロホルム又はベン
ゼン等に漬ける)し未露光部を溶解除去する。重合した
LB膜は現像液に対して不溶である。かくして重合LB
膜からなる導波路下部12が構築される(第2区(ハ)
)。
8. Next, it is developed (soaked in alcohol, chloroform, benzene, etc.) and the unexposed areas are dissolved and removed. The polymerized LB film is insoluble in developer. Thus polymerization LB
A lower waveguide 12 made of a film is constructed (second section (c)
).

4、導波路下部12の上に重合性LB膜18をLB法に
より付着形成せしめる(第2図に))。
4. A polymerizable LB film 18 is deposited on the lower part 12 of the waveguide by the LB method (see FIG. 2).

5、次いで、光等のエネルギー線11により重合性LB
膜18をグレーティングパターン露光する(第2図(ホ
))。
5. Next, polymerizable LB is formed by energy rays 11 such as light.
The film 18 is exposed in a grating pattern (FIG. 2 (e)).

6、現像により、未露光部を溶解除去する(第2図(へ
))。
6. The unexposed areas are dissolved and removed by development (Fig. 2(f)).

かくして、グレーティング型光結合器が得られる。In this way, a grating type optical coupler is obtained.

実施例1(第2図参照) 2.5−ジスチリルピラジンのピラジン環上にn−オク
タデカノイル基を導入した四級塩Aを成膜分子とし、表
面圧を一定に保ちながら表面が十分に清浄で親水性とな
っているガラス基板を水中に静かに上下させて単分子膜
を基板上に移しとり、50、100,200,800.
500層に累積した単分子累積膜(LB膜)を製造した
。生成膜はピラジン環側か基板に接している。
Example 1 (see Figure 2) The film forming molecule was quaternary salt A in which an n-octadecanoyl group was introduced onto the pyrazine ring of 2.5-distyrylpyrazine, and the surface was sufficiently coated while keeping the surface pressure constant. A monomolecular film was transferred onto the substrate by gently raising and lowering a clean, hydrophilic glass substrate into water, and then the monomolecular film was transferred onto the substrate at 50, 100, 200, 800.
A monomolecular stacked film (LB film) with 500 layers was manufactured. The produced film is in contact with the pyrazine ring side or the substrate.

第4図では、第1@10〜25、50、100 。In FIG. 4, the first @10-25, 50, 100.

150、200層に累積、第2層12〜25.50゜1
00、150、2009に累積。
Accumulated to 150, 200 layers, second layer 12~25.50°1
Accumulated on 00, 150, and 2009.

参考例1 実施例1で作成したLB膜パターンに従ってX線照射を
行ない、式■の様な重合を行ないパターニングによりグ
レーティングを形成した。
Reference Example 1 X-ray irradiation was carried out according to the LB film pattern prepared in Example 1, polymerization was carried out as shown in formula (2), and a grating was formed by patterning.

結果は、鋭いエッチが得られ高性能が発揮されなグレー
ティングピッチ最小200 X グレーティング深さ 0.1μ 実施例2 実施例1と同様にして、第1表に示す光重合性モノマー
を用いて、光結合器を製造した。
The results showed that sharp etching was obtained and high performance was not exhibited. Minimum grating pitch: 200 x grating depth: 0.1μ Example 2 In the same manner as Example 1, using the photopolymerizable monomers shown in Table 1, A coupler was manufactured.

本発明の特有の効果は下記の通りである。The unique effects of the present invention are as follows.

1.上述したLB膜の特質により、鋭(・エッヂの微小
形状を容易に形成できるので、レンズ性能の良い光結合
器を得ることができる。
1. Due to the above-mentioned characteristics of the LB film, a fine shape with sharp edges can be easily formed, so that an optical coupler with good lens performance can be obtained.

2、製作が容易であるため、製作コストが安価である。2. Since it is easy to manufacture, the manufacturing cost is low.

8、製作過程上、高温処理を要しないため耐熱性のない
組材を用いることができる。
8. Since high-temperature treatment is not required during the manufacturing process, non-heat resistant components can be used.

【図面の簡単な説明】[Brief explanation of drawings]

第1図はグレーティング型光結合器の断面図。 第2図(イ) 、 tcr+ 、(ハ)、に)9体)、
(へ)は本発明の製作例の断面図である。 l・・・光導波路、2・・・基板。 8・・・グレーティング、 4・・・導波光。 5・・・射出光、 6・・・モード・インデックスレン
ズ。 7・・・露光、 8.8’・・・非露光部(モノマLB
膜)9・・・LB膜(重合)lO・・・重合性LB膜。 11・・・導波路下部、12・・・重合性LB膜。 特許出願人 キャノン株式会社4 代理人 苦杯 、咽四
FIG. 1 is a sectional view of a grating type optical coupler. Figure 2 (a), tcr+, (c), ni) 9 bodies),
(f) is a sectional view of a manufacturing example of the present invention. l... Optical waveguide, 2... Substrate. 8... Grating, 4... Waveguide light. 5...Emission light, 6...Mode index lens. 7...Exposed, 8.8'...Non-exposed area (monomer LB
Membrane) 9...LB film (polymerization) lO...Polymerizable LB film. 11... lower part of waveguide, 12... polymerizable LB film. Patent Applicant: Canon Co., Ltd. 4 Agent: Kuwai, Hyoushi

Claims (1)

【特許請求の範囲】[Claims] グレーティングを設置した光導波路を有する光結合器に
おいて、該グレーティングを設置した光導波路が光重合
性オレフィン化合物の単分子累積膜からなることを特徴
とする光結合器。
1. An optical coupler having an optical waveguide provided with a grating, wherein the optical waveguide provided with the grating is made of a monomolecular cumulative film of a photopolymerizable olefin compound.
JP6485784A 1984-03-31 1984-03-31 Optical coupler Pending JPS60208711A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6485784A JPS60208711A (en) 1984-03-31 1984-03-31 Optical coupler

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6485784A JPS60208711A (en) 1984-03-31 1984-03-31 Optical coupler

Publications (1)

Publication Number Publication Date
JPS60208711A true JPS60208711A (en) 1985-10-21

Family

ID=13270268

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6485784A Pending JPS60208711A (en) 1984-03-31 1984-03-31 Optical coupler

Country Status (1)

Country Link
JP (1) JPS60208711A (en)

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