JPH052199A - Wavelength conversion element - Google Patents
Wavelength conversion elementInfo
- Publication number
- JPH052199A JPH052199A JP17777891A JP17777891A JPH052199A JP H052199 A JPH052199 A JP H052199A JP 17777891 A JP17777891 A JP 17777891A JP 17777891 A JP17777891 A JP 17777891A JP H052199 A JPH052199 A JP H052199A
- Authority
- JP
- Japan
- Prior art keywords
- crystal
- conversion element
- wavelength conversion
- group represented
- refractive index
- 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
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、光情報伝送技術分野、
光記録技術分野における光波長変換素子に関するもので
ある。The present invention relates to the field of optical information transmission technology,
The present invention relates to an optical wavelength conversion element in the field of optical recording technology.
【0002】[0002]
【従来の技術】有機物質の非線形光学特性が、既存の無
機化合物に比べて大きい事が近年知られてきた。一方光
記録分野では、記録読み取り、あるいは書き込み波長の
短波長化が、高密度記録の観点から必要とされてきてい
る。この目的のために、非線形光学特性の一つである第
二高調波発生(入射光の波長の半分の波長の光が発光す
る現象)が詳しく検討されており、例えば、「光エレク
トロニクスの基礎」A.YARIV著、多田邦雄、神谷
武志訳(丸善株式会社)のp250−259に示される
様な全体結晶型のものがよく用いられている。しかしな
がら、この様な状態での波長変換の機作は、結晶の複屈
折を利用した位相整合条件を満足した時にのみ、活性が
高くなるという現象であり、この条件を揃えるための、
空間配置の決定など、非常に煩雑な操作が必要であり、
かつ外部温度、湿度により複屈折の挙動が変化する事も
多く、実用上問題が多い。2. Description of the Related Art In recent years, it has been known that the nonlinear optical characteristics of organic substances are larger than those of existing inorganic compounds. On the other hand, in the field of optical recording, recording / reading or shortening of the writing wavelength has been required from the viewpoint of high density recording. For this purpose, the second harmonic generation (a phenomenon in which light having a wavelength half the wavelength of the incident light is emitted), which is one of the nonlinear optical characteristics, has been studied in detail. A. YARIV, Kunio Tada, Takeshi Kamiya translation (Maruzen Co., Ltd.) p250-259 is generally used. However, the mechanism of wavelength conversion in such a state is a phenomenon that the activity becomes high only when the phase matching condition utilizing the birefringence of the crystal is satisfied, and in order to arrange this condition,
Very complicated operations are required, such as determining the space layout,
In addition, the behavior of birefringence often changes depending on the external temperature and humidity, which is a problem in practical use.
【0003】上記の様な問題点を解決する方法として、
導波路型の素子を作成し、一定方向への第二高調波の発
生を容易にするチェレンコフ放射の検討が行われてい
る。As a method for solving the above problems,
Cherenkov radiation has been studied for making a waveguide type device and facilitating generation of the second harmonic in a certain direction.
【0004】特にこの場合、非線形光学現象を生起する
材料の形態が第二高調波発生に大きな効果を示し、変換
効率の向上にこの制御が必須の技術となる。特に、波長
の変換効率は、レーザ光のパワー密度に比例するので、
できるだけ入射光を閉じ込める工夫が必要になる。ま
た、一般に無機材料よりも非線形光学特性が優れている
といわれる有機材料も、その固体構造中での分子の空間
配置の変化で、完全に本来の性能を発現させるには至ら
ないこともある。本発明は、大きな非線形光学特性を有
する新規な材料を用い、かかる欠点を除去して、有機材
料の固体配向を制御して高い効率を有する波長変換素
子、を提供することにある。In this case, in particular, the form of the material that causes the nonlinear optical phenomenon has a great effect on the generation of the second harmonic, and this control is an essential technique for improving the conversion efficiency. Especially, since the wavelength conversion efficiency is proportional to the power density of the laser light,
It is necessary to devise to confine incident light as much as possible. In addition, an organic material, which is generally said to have better nonlinear optical characteristics than an inorganic material, may not fully exhibit its original performance due to a change in the spatial arrangement of molecules in the solid structure. The present invention aims to provide a wavelength conversion element having a high efficiency by controlling a solid orientation of an organic material by using a novel material having a large non-linear optical property and eliminating such a defect.
【0005】[0005]
【発明の構成】即ち、本発明は、非線形光学特性を有す
る有機結晶及び該結晶よりも低屈折率の支持体からなる
導波型の波長変換素子に関するものである。本発明の波
長変換素子は結晶部分に基本波を入射し、入射光波長を
第二高調波に変換し、導波させることを特徴とする。本
発明に用いられる非線形光学結晶は、下記一般式(1)
で表されるカルボン酸の光学活性アミン塩であることが
好適である。That is, the present invention relates to a waveguide type wavelength conversion element comprising an organic crystal having nonlinear optical characteristics and a support having a refractive index lower than that of the crystal. The wavelength conversion element of the present invention is characterized in that a fundamental wave is incident on a crystal part, the incident light wavelength is converted into a second harmonic, and the second harmonic is guided. The nonlinear optical crystal used in the present invention has the following general formula (1).
An optically active amine salt of a carboxylic acid represented by
【0006】
R1 -Ar-(CH=CH) n -CH=C(CN)-COOH (1)
[但しnは、0,1または2を表す。Arは、炭素数5
〜14の芳香族基を表す。R1 −は、R2 R3 N−で表
されるアミノ基、R4 −O−で表されるエーテル基、R
5 −S−で表されるチオエーテル基、ニトリル基、−C
OOR6 ,−OCOR7 で表されるエステル基、−CO
NR8 R9 ,−NR10COR11で表されるアミド基、−
R12で表される炭化水素基(R2 〜R12は、同一,ある
いは異なる炭素数1〜8の炭化水素基、または水素原子
を表す)から選ばれる官能基である]本発明に用いられ
る光学活性アミンは、1−フェニルエチルアミン、1−
α−ナフチルアミン、1−フェニル−2−メチルエチル
アミン、1−フェニル−2−アミノプロパン、ブルシ
ン、から選ばれる一種であることが好適である。R 1 -Ar- (CH = CH) n -CH = C (CN) -COOH (1) [where n represents 0, 1 or 2] Ar has 5 carbon atoms
~ 14 aromatic groups. R 1 -is an amino group represented by R 2 R 3 N-, an ether group represented by R 4 -O-, R
5 -thio group represented by -S-, nitrile group, -C
An ester group represented by OOR 6 and -OCOR 7 , -CO
NR 8 R 9, amido group represented by -NR 10 COR 11, -
A hydrocarbon group represented by R 12 (R 2 to R 12 are functional groups selected from the same or different hydrocarbon groups having 1 to 8 carbon atoms, or a hydrogen atom)] Used in the present invention The optically active amines are 1-phenylethylamine, 1-
It is preferably one selected from α-naphthylamine, 1-phenyl-2-methylethylamine, 1-phenyl-2-aminopropane and brucine.
【0007】非線形光学特性を有するカルボン酸アミン
塩として、4−ジメチルアミノフェニルペンタジエノン
酸のL−(−)−フェニルエチルアミン塩が好適であ
る。L-(-)-phenylethylamine salt of 4-dimethylaminophenylpentadienenoic acid is preferable as the carboxylic acid amine salt having nonlinear optical characteristics.
【0008】かかる材料の作成については、例えば、特
開平1−245230号公報(平成1年9月29日公
開)に示される様に、芳香族アルデヒドと活性メチレン
化合物との反応で得られるα−シアノアクリル酸化合物
を、上に述べた光学活性アミンと反応させることで調製
出来る。上記一般式のカルボン酸の光学活性塩は、極性
溶媒に溶解後、溶媒を緩慢に蒸発させるスローエバポレ
ーション法により結晶に作成することが出来る。本発明
に記載の波長変換素子の作成には、これらの結晶を別途
他の空間で作成した後に、屈折率がこの結晶よりも小さ
い支持体に装着することでも作成出来るが、あらかじ
め、数mmから、数μの間隔を調製した2枚の基板のす
きまに、毛管現象を利用することで、溶液を展開静置、
溶媒を蒸発させることで基板と一体の成形品を得る事が
出来る。支持体材料としては、非線形光学材料の屈折率
よりも小さい事が必須で、通常は、各種ガラス材料、と
りわけケイほう酸ガラスが好ましく使われる。この支持
体の非線形光学材料と接する表面に、予め、溝を作成し
ておくことで、成形の一体化が容易となることもある。Regarding the preparation of such a material, as shown in, for example, Japanese Patent Application Laid-Open No. 1-245230 (published on September 29, 1991), α-obtained by the reaction of an aromatic aldehyde with an active methylene compound. It can be prepared by reacting a cyanoacrylic acid compound with the optically active amine described above. The optically active salt of a carboxylic acid represented by the above general formula can be formed into crystals by a slow evaporation method in which a solvent is slowly evaporated after being dissolved in a polar solvent. In the production of the wavelength conversion element according to the present invention, these crystals can be produced separately in another space and then mounted on a support whose refractive index is smaller than this crystal. , By using the capillary phenomenon in the gap between the two substrates with the spacing of several μ adjusted, the solution is allowed to stand still,
By evaporating the solvent, a molded product integrated with the substrate can be obtained. As the support material, it is essential that it is smaller than the refractive index of the nonlinear optical material, and various glass materials, particularly silica borate glass, are preferably used. Forming grooves in advance on the surface of the support in contact with the nonlinear optical material may facilitate the integration of molding.
【0009】[0009]
【発明の効果】本発明に述べられる波長変換素子は、入
射光の波長が単一の時には、入射光の波長が半分になる
第二高調波発生となり、例えば、CD読み取りで用いら
れている800mμ付近の発光波長の半導体レーザを入
力光源に用いれば、400mμの発光が生起し、従来の
読み取り密度を3−4倍に向上することが可能となる。
また、入射光源の種類を2種類の異なる波長のものを用
いれば、両方の波長の逆数の和のさらに逆数となる波
長、一般に長波長の発光が生起する光学素子としても使
用可能である。When the wavelength of the incident light is single, the wavelength conversion element described in the present invention generates the second harmonic wave in which the wavelength of the incident light is halved. For example, 800 mμ used in CD reading. If a semiconductor laser having a light emission wavelength in the vicinity is used as an input light source, light emission of 400 mμ occurs, and the conventional reading density can be improved 3 to 4 times.
Further, if two types of incident light sources having different wavelengths are used, it can be used as an optical element which emits light having a wavelength which is a reciprocal of the sum of the reciprocals of both wavelengths, generally a long wavelength.
【0010】[0010]
【実施例】以下、実施例により本発明を詳述する。EXAMPLES The present invention will be described in detail below with reference to examples.
【実施例1】非線形光学特性を有するカルボン酸アミン
塩として、4−ジメチルアミノフェニルペンタジエノン
酸のL−(−)−フェニルエチルアミン塩を用い、この
粉末500mgをメタノール10mlに溶解した溶液を
作成し、この溶液に20ミクロンのポリエチレンテレフ
タレートのフィルムをはさんだ2枚のケイほう酸ガラス
(屈折率 1.46)に図1に示したように片側を浸漬
する。毛細管現象で上昇してくる溶液をはさんだ2枚の
基板を室温で約7日間静置した。基板の隙間に約2mm
×10mm程度の板状の結晶の析出が認められた。この
部分に、図2で示した様に、波長1.06μのヤグレー
ザを入射したところ、他の端面から、緑色の光が観測さ
れた。この発光のスペクトルをマルチチャンネルホトデ
テクターで波長スキャンの測定を行った結果を図3に示
した。この図よりこの発光が、入射光の1/2波長から
成り立っており、励起に伴う燐光、蛍光で無いことが確
認された。Example 1 L-(-)-phenylethylamine salt of 4-dimethylaminophenylpentadienenoic acid was used as a carboxylic acid amine salt having non-linear optical characteristics, and a solution was prepared by dissolving 500 mg of this powder in 10 ml of methanol. Then, as shown in FIG. 1, one side is dipped in two pieces of silicoborate glass (refractive index: 1.46) sandwiching a 20 micron polyethylene terephthalate film in this solution. The two substrates with the solution rising due to the capillary phenomenon sandwiched therein were allowed to stand at room temperature for about 7 days. About 2 mm in the gap between the boards
Precipitation of plate-like crystals of about × 10 mm was observed. As shown in FIG. 2, when a YAG laser having a wavelength of 1.06 μ was incident on this portion, green light was observed from the other end face. The spectrum of this emission was measured by a wavelength scan with a multi-channel photo detector, and the result is shown in FIG. From this figure, it was confirmed that this emission consists of 1/2 wavelength of the incident light and is not phosphorescence or fluorescence accompanying excitation.
【0011】[0011]
【実施例2】非線形光学特性を有するカルボン酸アミン
塩として、α−シアノ−p−ジメチルアミノケイヒ酸の
1−α−ナフチルアミン塩を用いて、実施例1と同様
に、2枚のケイほう酸ガラスの隙間に結晶化を行い、約
2mm×8mm程度の大きさの板状結晶をはさむ素子を
作成した。この端面に、1.06μのレーザ光を入射し
たところ、他の端面から緑色の発光が観測された。Example 2 As a carboxylic acid amine salt having a non-linear optical characteristic, 1-α-naphthylamine salt of α-cyano-p-dimethylaminocinnamic acid was used, and two pieces of silicoboric acid glass were used as in Example 1. Crystallization was performed in the gap to prepare an element sandwiching a plate crystal having a size of about 2 mm × 8 mm. When a laser beam of 1.06 μm was incident on this end face, green light emission was observed from the other end faces.
【0012】[0012]
【実施例3】非線形光学特性を有するカルボン酸アミン
塩として、α−シアノ−p−メトキシフェニルプロペノ
ン酸の1−α−ナフチルアミン塩を用いて、実施例1と
同様に、2枚のケイほう酸ガラスの隙間に結晶化を行
い、約3mm×5mm程度の大きさの板状結晶をはさむ
素子を作成した。この端面に、0.83μのレーザ光を
入射したところ、他の端面からの発光をマルチチャンネ
ルホトデテクターで波長スキャンの測定を行った結果
0.42μの波長で有ることが確認された。Example 3 Using 1-α-naphthylamine salt of α-cyano-p-methoxyphenylpropenoic acid as a carboxylic acid amine salt having nonlinear optical properties, two pieces of silicoboric acid were used in the same manner as in Example 1. Crystallization was carried out in the gaps between the glass to prepare an element sandwiching a plate crystal having a size of about 3 mm × 5 mm. When 0.83μ of laser light was incident on this end face, the emission of light from the other end face was measured by wavelength scanning with a multi-channel photodetector. As a result, it was confirmed that the wavelength was 0.42μ.
【図1】波長変換素子の作成方法の概念を示す。FIG. 1 shows a concept of a method for producing a wavelength conversion element.
【図2】波長変換素子の機作を示す概念図である。FIG. 2 is a conceptual diagram showing a mechanism of a wavelength conversion element.
【図3】実施例1における、波長変換素子の発光スペク
トルを示す。FIG. 3 shows an emission spectrum of the wavelength conversion element in Example 1.
1 非線形光学結晶 2 支持基板 3 非線形材料の溶液 10 入射光 11 出射光 12 レーザー光源 13 集光レンズ 1 Non-linear optical crystal 2 Support substrate 3 Non-linear material solution 10 incident light 11 Outgoing light 12 Laser light source 13 Condensing lens
Claims (3)
結晶よりも低屈折率の支持体からなる導波型の波長変換
素子。1. A waveguide type wavelength conversion element comprising an organic crystal having nonlinear optical characteristics and a support having a refractive index lower than that of the crystal.
が、下記一般式(1) R1 -Ar-(CH=CH) n -CH=C(CN)-COOH(1) [但しnは、0,1または2を表す。Arは、炭素数5
〜14の芳香族基を表す。R1 −は、R2 R3 N−で表
されるアミノ基、R4 −O−で表されるエーテル基、R
5 −S−で表されるチオエーテル基、ニトリル基、−C
OOR6 ,−OCOR7 で表されるエステル基、−CO
NR8 R9 ,−NR10COR11で表されるアミド基、−
R12で表される炭化水素基(R2 〜R12は、同一,ある
いは異なる炭素数1〜8の炭化水素基、または水素原子
を表す)から選ばれる官能基である]で表されるカルボ
ン酸の光学活性アミン塩であることを特徴とする請求項
1記載の波長変換素子。2. The organic crystal having the non-linear optical characteristics is represented by the following general formula (1) R 1 -Ar- (CH = CH) n -CH = C (CN) -COOH (1) [where n is 0 , 1 or 2 is represented. Ar has 5 carbon atoms
~ 14 aromatic groups. R 1 -is an amino group represented by R 2 R 3 N-, an ether group represented by R 4 -O-, R
5 -thio group represented by -S-, nitrile group, -C
An ester group represented by OOR 6 and -OCOR 7 , -CO
NR 8 R 9, amido group represented by -NR 10 COR 11, -
A hydrocarbon group represented by R 12 (R 2 to R 12 are functional groups selected from the same or different hydrocarbon groups having 1 to 8 carbon atoms, or a hydrogen atom)] The wavelength conversion element according to claim 1, which is an optically active amine salt of an acid.
が、1−フェニルエチルアミン、1−α−ナフチルアミ
ン、1−フェニル−2−メチルエチルアミン、1−フェ
ニル−2−アミノプロパン、ブルシン、から選ばれる一
種であることを特徴とする請求項2記載の波長変換素
子。3. The optically active amine according to claim 2, selected from 1-phenylethylamine, 1-α-naphthylamine, 1-phenyl-2-methylethylamine, 1-phenyl-2-aminopropane and brucine. The wavelength conversion element according to claim 2, wherein the wavelength conversion element is one type.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17777891A JPH052199A (en) | 1991-06-24 | 1991-06-24 | Wavelength conversion element |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17777891A JPH052199A (en) | 1991-06-24 | 1991-06-24 | Wavelength conversion element |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH052199A true JPH052199A (en) | 1993-01-08 |
Family
ID=16036953
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17777891A Pending JPH052199A (en) | 1991-06-24 | 1991-06-24 | Wavelength conversion element |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH052199A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994009403A1 (en) * | 1992-10-20 | 1994-04-28 | Fujitsu Limited | Application of optical system to phase conjugate optics |
CN101546887A (en) * | 2009-05-07 | 2009-09-30 | 吉林大学 | Method for realizing laser emission conversion on organic crystal frequency through multi-photon pumping |
-
1991
- 1991-06-24 JP JP17777891A patent/JPH052199A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994009403A1 (en) * | 1992-10-20 | 1994-04-28 | Fujitsu Limited | Application of optical system to phase conjugate optics |
US5596667A (en) * | 1992-10-20 | 1997-01-21 | Fujitsu Limited | Application of phase conjugate optics to optical systems |
CN101546887A (en) * | 2009-05-07 | 2009-09-30 | 吉林大学 | Method for realizing laser emission conversion on organic crystal frequency through multi-photon pumping |
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