JPH04204906A - Multilayer thin film optical element - Google Patents
Multilayer thin film optical elementInfo
- Publication number
- JPH04204906A JPH04204906A JP33942990A JP33942990A JPH04204906A JP H04204906 A JPH04204906 A JP H04204906A JP 33942990 A JP33942990 A JP 33942990A JP 33942990 A JP33942990 A JP 33942990A JP H04204906 A JPH04204906 A JP H04204906A
- Authority
- JP
- Japan
- Prior art keywords
- oxide
- refractive index
- prism
- optical member
- thin film
- 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.)
- Granted
Links
- 230000003287 optical effect Effects 0.000 title claims abstract description 22
- 239000010409 thin film Substances 0.000 title claims description 7
- 239000000853 adhesive Substances 0.000 claims abstract description 20
- 230000001070 adhesive effect Effects 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims abstract description 18
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000010408 film Substances 0.000 claims description 5
- MMKQUGHLEMYQSG-UHFFFAOYSA-N oxygen(2-);praseodymium(3+) Chemical compound [O-2].[O-2].[O-2].[Pr+3].[Pr+3] MMKQUGHLEMYQSG-UHFFFAOYSA-N 0.000 claims description 3
- 229910003447 praseodymium oxide Inorganic materials 0.000 claims description 3
- 239000005083 Zinc sulfide Substances 0.000 claims 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 claims 1
- 229910001634 calcium fluoride Inorganic materials 0.000 claims 1
- 229910000420 cerium oxide Inorganic materials 0.000 claims 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims 1
- 239000000395 magnesium oxide Substances 0.000 claims 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 claims 1
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 claims 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims 1
- 229910052984 zinc sulfide Inorganic materials 0.000 claims 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 claims 1
- 229910001928 zirconium oxide Inorganic materials 0.000 claims 1
- 238000007740 vapor deposition Methods 0.000 abstract description 8
- 239000000203 mixture Substances 0.000 abstract description 7
- 239000011521 glass Substances 0.000 abstract description 5
- 229910052746 lanthanum Inorganic materials 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- 229910052726 zirconium Inorganic materials 0.000 abstract description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 26
- 238000002834 transmittance Methods 0.000 description 10
- 230000003595 spectral effect Effects 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000012788 optical film Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- 229910052777 Praseodymium Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000007737 ion beam deposition Methods 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000005240 physical vapour deposition Methods 0.000 description 1
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000001947 vapour-phase growth Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、光学メモリヘッドや、カラー複写機、TVプ
ロジェクション装置に用いられる各種のプリズム形状を
有するビームスプリッタに関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a beam splitter having various prism shapes used in optical memory heads, color copying machines, and TV projection devices.
TVプロジェクション装置やカラー複写機には光源から
所望の色光をとり出すために“グイクロイックフィルタ
ー”と称するビームスプリッタが使用されている。また
、近年注目されている光メモリ装置の読み取り光学系、
書き込み光学系にも多くのビームスプリッタが利用され
ている。これらビームスプリッタは担体光学部材として
所定形状に加工されたプリズム(以下担体ガラスプリズ
ム又は担体プリズム又は単にプリズムと言うことがある
。)の面上に、複数の誘電体薄膜を積層し、その後、こ
のプリズム面に、別のプリズムを接合し、作製すること
が多い。そして、2つのプリズムを接合するために用い
られる接合剤として熱硬化型と紫外線硬化型の2種類が
ある。この2種の接着剤を作業性、生産効率の点から比
較してみると、まず熱硬化型接着剤は、
1)2つのプリズム閤に介在した熱硬化型接着剤は加圧
、加熱されることにより、接着剤の粘度か低くなりプリ
ズムと接着治具との間に流込み、プリズムと接着治具と
が接着されて、取外しが困難であるばかりか、プリズム
が破損することもある、2)治具で2つのプリズムを位
置合せした状態で加熱するため、治具に熱応力、熱膨張
が発生し、プリズム相互の位置ずれを起し易い、
3)接着時に気泡等が発生すると再生が困難である、
4)接着剤の種類により多少異なるが、−数的に紫外線
硬化型にくらべ硬化時間を長く必要とする、という欠点
を持つ。A beam splitter called a "gichroic filter" is used in TV projection devices and color copying machines to extract desired colored light from a light source. In addition, the reading optical system of optical memory devices, which has been attracting attention in recent years,
Many beam splitters are also used in writing optical systems. These beam splitters are made by laminating a plurality of dielectric thin films on the surface of a prism processed into a predetermined shape as a carrier optical member (hereinafter sometimes referred to as a carrier glass prism, a carrier prism, or simply a prism). It is often manufactured by bonding another prism to the prism surface. There are two types of bonding agents used to bond two prisms: a thermosetting type and an ultraviolet curing type. Comparing these two types of adhesives in terms of workability and production efficiency, the thermosetting adhesive is: 1) The thermosetting adhesive sandwiched between the two prisms is pressurized and heated. As a result, the viscosity of the adhesive becomes low and it flows between the prism and the adhesive jig, causing the prism and the adhesive jig to be glued together, making it difficult to remove and even damaging the prism. ) Since the two prisms are heated while aligned using a jig, thermal stress and thermal expansion occur in the jig, which tends to cause the prisms to become misaligned. 3) If air bubbles occur during adhesion, regeneration may occur. 4) Although it differs somewhat depending on the type of adhesive, it has the disadvantage of - Numerically, it requires a longer curing time than the ultraviolet curing type.
これに対し、紫外線硬化型接着剤は次のような長所をも
つ。In contrast, UV-curable adhesives have the following advantages.
1)仮固定(数秒〜lO数秒の紫外線照射)の状態で接
着治具から偏光ビームスプリッタを取出すため、取外し
が容易でありプリズムの破損が少ない。1) Since the polarizing beam splitter is removed from the adhesive jig while temporarily fixed (UV irradiation for several seconds to several seconds), removal is easy and damage to the prism is less likely.
2)接着治具を加熱する必要がない為、プリズム相互の
位置ずれが起こりにくい。2) Since there is no need to heat the adhesive jig, misalignment of the prisms is less likely to occur.
仮固定の状態で位置ずれ、気泡の発生時の検査か可能で
あり、仮に位置ずれ、気泡が発生しても容易に再生する
ことができる。It is possible to inspect the occurrence of misalignment or bubbles while temporarily fixed, and even if misalignment or bubbles occur, it can be easily regenerated.
3)接着治具は、仮固定までしか使わないため、治具の
回転効率が高い。3) Since the adhesive jig is used only for temporary fixing, the rotation efficiency of the jig is high.
以上のように、量産という面からみると、紫外線硬化型
接着剤の方が、圧倒的に有利である。しかし、紫外線を
用いて接合を行なうと、積層膜の特性が大きく変化して
しまうという欠点がある。As mentioned above, from the perspective of mass production, UV-curable adhesives are overwhelmingly advantageous. However, when bonding is performed using ultraviolet light, there is a drawback that the properties of the laminated film change significantly.
特に、蒸着物質に酸化チタニウムを使用した場合顕著で
ある。This is particularly noticeable when titanium oxide is used as the vapor deposition material.
゛本発明の目的は、量産上の作業性、効率に優れた紫外
線硬化型接着剤を用いる接合法によっても特性が損なわ
れることのない積層光学膜を提供することにある。An object of the present invention is to provide a laminated optical film whose properties are not impaired even by a bonding method using an ultraviolet curable adhesive that is excellent in workability and efficiency in mass production.
前記本発明の目的は、担体光学部材面に高屈折率層と低
屈折率層とを積層、担持させ、その形成された積層膜を
差挟んで、紫外線硬化型接着剤で接合光学部材面を接合
した多層薄膜光学素子において、少くとも前記接合光学
部材面に最も近い2層のうち一層が酸化プラセオジムと
酸化チタニウムとを含有している混成物質の層であるこ
とを特徴とする多層薄膜光学素子によって達成される。The object of the present invention is to laminate and support a high refractive index layer and a low refractive index layer on the optical member surface of a carrier, sandwich the formed laminated film, and bond the optical member surface with an ultraviolet curable adhesive. In the bonded multilayer thin film optical element, at least one of the two layers closest to the surface of the bonded optical member is a layer of a hybrid material containing praseodymium oxide and titanium oxide. achieved by
また積層数は必要に応し任意に定めつるが、本発明にお
いては接合光学部材面に最も近い2層のうち一層が前記
混成層であれば充分であるが、できるだけ多くの混成層
を用いることが好ましい。The number of laminated layers can be arbitrarily determined according to need, but in the present invention, it is sufficient if one of the two layers closest to the bonded optical member surface is the above hybrid layer, but it is preferable to use as many hybrid layers as possible. is preferred.
また該混成層においてプラセオジウム/チタニウムの比
は0.5〜5、好ましくは2〜3である。Further, the praseodymium/titanium ratio in the hybrid layer is 0.5 to 5, preferably 2 to 3.
更にZr、 Ta、 Y、 La等の金属及び/又はそ
れらの酸化物が特性を損わぬ範囲含有されていてもよい
。Furthermore, metals such as Zr, Ta, Y, La, etc. and/or oxides thereof may be contained within a range that does not impair the properties.
尚接着剤の層のみを介して接合光学部材面に直面、する
積層光学膜の層は積層数に応じ高屈折率層であっても低
屈折率層であっても差支えない。The layer of the laminated optical film facing the surface of the bonded optical member through only the adhesive layer may be a high refractive index layer or a low refractive index layer depending on the number of laminated layers.
また積層光学膜の形成には各種の気相堆積法、例えば真
空蒸着、スパッタリング、イオンビーム蒸着等の物理蒸
着法或は反応ガスを制御しながらのCVD法等が任意に
用いられる。Further, various vapor phase deposition methods such as vacuum deposition, sputtering, physical vapor deposition such as ion beam deposition, or CVD method while controlling a reaction gas can be used as desired to form the laminated optical film.
次に実施例によって本発明を具体的に説明する。 Next, the present invention will be specifically explained with reference to Examples.
まず本実施例を説明する前に次に比較例を上げる。First, before explaining this example, a comparative example will be described next.
30°入射の青反射グイクロイックフィルターを作った
。高屈折率層用蒸着材料としてTiO*、低屈折率層用
蒸着材料として^1!0.を用いた。各材料は、表1の
蒸着条件の下で第2図及び表2に示すような層構成に蒸
着した。I made a blue reflection gichroic filter with 30° incidence. TiO* is used as the vapor deposition material for the high refractive index layer, and ^1!0. is used as the vapor deposition material for the low refractive index layer. was used. Each material was deposited under the deposition conditions shown in Table 1 to form a layer structure as shown in FIG. 2 and Table 2.
表 1
表 2
注)材料 T =Tilt A = AItO+蒸着
後、大気中にプリズムをとり出し、別の蒸着されていな
いプリズムを第1図のように貼りあわせた。プリズムの
貼り合わせには紫外線硬化型接着剤を用い、その接合条
件は表3のようであった。Table 1 Table 2 Note) Materials T = Tilt A = AItO + After the vapor deposition, the prism was taken out into the atmosphere and another prism that had not been vapor deposited was attached as shown in Figure 1. An ultraviolet curing adhesive was used to bond the prisms together, and the bonding conditions were as shown in Table 3.
第3図に、仮固定後(曲線a)と本硬化後(曲線b)の
分光透過率を示す。第3図より明らかに、本硬化後透過
率が低下していることがわかる。FIG. 3 shows the spectral transmittance after temporary fixation (curve a) and after main curing (curve b). It is clearly seen from FIG. 3 that the transmittance decreases after main curing.
〔実施例1〕
プラセオジウム酸化物とチタン酸化物とを主成分とする
混合物(例えば[!、 Merck社製商品名“サブス
タンス2” 二以下混合物という)を高屈折率物質、A
lxOsを低屈折率物質として、担体光学部材としての
担体ガラスプリズム(材質・BK7)上に真空蒸着によ
り、交互に33層積層した。蒸着開始真空度はI X
10−’Torr基板加熱温度は350℃であった。前
述の表1に示す蒸着条件に従い、冬物表4
蒸着後、プリズムを大気中に取出し、−接合ガラ−スプ
リズム(材質: BK7)と、紫外線硬化型接着剤を用
いて、前述の表3の接合条件により第4図及び第5図に
示すように接合した。[Example 1] A mixture containing praseodymium oxide and titanium oxide as main components (for example, [!, product name “Substance 2” manufactured by Merck Company, referred to as a mixture of two or less)] was used as a high refractive index substance, A
Thirty-three layers of lxOs as a low refractive index substance were alternately stacked on a carrier glass prism (material: BK7) as a carrier optical member by vacuum deposition. The vacuum level at the start of evaporation is I
The 10-'Torr substrate heating temperature was 350°C. According to the vapor deposition conditions shown in Table 1 above, the prism was taken out into the atmosphere and bonded as shown in Table 3 above using a bonded glass prism (material: BK7) and an ultraviolet curing adhesive. Depending on the conditions, bonding was carried out as shown in FIGS. 4 and 5.
仮固定後と、本硬化後のこのプリズムの分光透過率i第
6図に示すが両者の間に、差は認められなかった。゛
(実施例2〕
実施例1と同じ物質を第7図第8図に示すように担体ガ
ラスプリズム(材質: BK7)上に積層し、紫外線硬
化接着剤を用いて接合プリズムと接合し、青反射グイク
ロイックフィルターを作成した。蒸着条件、接合条件は
実施例1と同じで積層膜は第7図及び表5に示す構成で
19層からなっている。The spectral transmittance i of this prism after temporary fixing and after main curing is shown in FIG. 6, and no difference was observed between the two. (Example 2) The same material as in Example 1 was laminated on a carrier glass prism (material: BK7) as shown in Figs. A reflective gichroic filter was prepared.The vapor deposition conditions and bonding conditions were the same as in Example 1, and the laminated film consisted of 19 layers with the configuration shown in FIG. 7 and Table 5.
注)材料棚 A = AI!0* M =混合物仮固
定後と本硬化後に、積層膜に入射角30″で光を入射さ
せ、分光透過率を測定したが第9図に示すようにまった
く差異は生じなかった。Note) Material shelf A = AI! 0*M = After the mixture was temporarily fixed and after it was fully cured, light was incident on the laminated film at an incident angle of 30'' and the spectral transmittance was measured, but as shown in FIG. 9, there was no difference at all.
〔実施例3〕
実施例2と同じ形状の担体プリズム上に第1O図及び表
6に示すようにTie、とAIJ*を交互に19層蒸着
し、さらにその上に混合物とA110mを交互に9層蒸
着した。各材料の蒸着条件は前述の表1の通りである。[Example 3] On a carrier prism having the same shape as in Example 2, 19 layers of Tie and AIJ* were alternately deposited as shown in Figure 1O and Table 6, and further 9 layers of the mixture and A110m were alternately deposited on top of that. Layers were deposited. The vapor deposition conditions for each material are as shown in Table 1 above.
注)材料欄 A : Altos T : Ti1t
M :混合物蒸着後このプリズムを取り出し、第1図
に示すように別の接合プリズム(材質BK?)と接合し
、赤反射ダイクロイックプリズムを作成した。接合は表
1の条件に従った。Note) Material column A: Altos T: Ti1t
M: After the mixture was deposited, this prism was taken out and bonded with another bonded prism (made of BK?) as shown in FIG. 1 to create a red reflective dichroic prism. The bonding was carried out according to the conditions shown in Table 1.
実施例2と同一条件で仮固定後と、本硬化後にプリズム
の分光透過率特性を調べたが差異は第12図に示すよう
に生じていなかった。The spectral transmittance characteristics of the prism were examined after temporary fixing and after main curing under the same conditions as in Example 2, but no difference was found as shown in FIG.
複数の誘電体薄膜を積層したプリズムの積層面に他のプ
リズムを紫外線硬化型接着剤で接合してダイクロイック
フィルターを作り、所望の色光を光源から取出す場合、
本発明の積層物質の混成層を施すことにより、該ダイク
ロイックフィルターの前記接着による透過率光学特性の
変動現象を解消できるようになった。When creating a dichroic filter by bonding another prism to the laminated surface of a prism made of multiple dielectric thin films with an ultraviolet curing adhesive, and extracting the desired colored light from a light source,
By applying the composite layer of the laminated material of the present invention, it has become possible to eliminate the phenomenon of variation in transmittance optical characteristics due to the adhesion of the dichroic filter.
第1図はダイクロイックフィルターの断面図。
第2図は従来の比較例のダイクロイックフィルターの層
構成断面図。
第3図は従来の比較例のダイクロイツタフィルターの分
光透過率曲線。
第4図は実施例1のダイクロイックフィルターの層−構
成の断面図。
第5図は実施例1のダイクロイックフィルターの断面図
。
第6図は実施例1のダイクロイックフィルターの分光透
過率曲線。
第7図は実施例2のダイクロイックフィルターの層構成
断面図。
第8図は実施例2のダイクロイックフィルターの断面図
。
第9図は実施例2のダイクロイックフィルターの分光透
過率曲線。
第10図は実施例3のダイクロイックフィルターの層構
成断面図。
第11図は実施例3のダイクロイックフィルターの断面
図。
第12図は実施例3のダイクロイックフィルターの分光
透過率曲線。Figure 1 is a cross-sectional view of a dichroic filter. FIG. 2 is a cross-sectional view of the layer structure of a conventional dichroic filter as a comparative example. Figure 3 shows the spectral transmittance curve of a conventional Dichroi Ivy filter as a comparative example. FIG. 4 is a sectional view of the layer structure of the dichroic filter of Example 1. FIG. 5 is a sectional view of the dichroic filter of Example 1. FIG. 6 is a spectral transmittance curve of the dichroic filter of Example 1. FIG. 7 is a sectional view of the layer structure of the dichroic filter of Example 2. FIG. 8 is a sectional view of the dichroic filter of Example 2. FIG. 9 is a spectral transmittance curve of the dichroic filter of Example 2. FIG. 10 is a sectional view of the layer structure of the dichroic filter of Example 3. FIG. 11 is a sectional view of the dichroic filter of Example 3. FIG. 12 is a spectral transmittance curve of the dichroic filter of Example 3.
Claims (2)
層、担持させ、その形成された積層膜を差しはさんで紫
外線硬化型接着剤で接合光学部材面を接合した多層薄膜
光学素子において、少なくとも前記接合光学部材面に最
も近い2層のうち1層が、酸化プラセオジウムと酸化チ
タニウムとを含有している混合物質の層であることを特
徴とする多層薄膜光学素子。(1) A multilayer thin film in which a high refractive index layer and a low refractive index layer are laminated and supported on the carrier optical member surface, and the optical member surface is bonded with an ultraviolet curing adhesive by sandwiching the formed laminated film. A multilayer thin film optical element, wherein at least one of the two layers closest to the bonded optical member surface is a layer of a mixed material containing praseodymium oxide and titanium oxide.
硫化亜鉛、酸化ジルコニウム、酸化セリウムのいづれか
を用い、低屈折率層として、酸化アルミニウム、酸化イ
ットリウム、酸化マグネシウム、フッ化カルシウムのい
づれかを用いたことを特徴とする請求項1記載の多層薄
膜光学素子。(2) As the high refractive index layer, the hybrid layer, titanium oxide,
2. The multilayer thin film optical element according to claim 1, wherein one of zinc sulfide, zirconium oxide, and cerium oxide is used, and one of aluminum oxide, yttrium oxide, magnesium oxide, and calcium fluoride is used as the low refractive index layer. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2339429A JP2881498B2 (en) | 1990-11-30 | 1990-11-30 | Multilayer thin film optical element |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2339429A JP2881498B2 (en) | 1990-11-30 | 1990-11-30 | Multilayer thin film optical element |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04204906A true JPH04204906A (en) | 1992-07-27 |
JP2881498B2 JP2881498B2 (en) | 1999-04-12 |
Family
ID=18327386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2339429A Expired - Lifetime JP2881498B2 (en) | 1990-11-30 | 1990-11-30 | Multilayer thin film optical element |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2881498B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002034913A (en) * | 2000-07-27 | 2002-02-05 | Asahi Optical Co Ltd | Optical system of light source device in electronic endoscope system |
-
1990
- 1990-11-30 JP JP2339429A patent/JP2881498B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002034913A (en) * | 2000-07-27 | 2002-02-05 | Asahi Optical Co Ltd | Optical system of light source device in electronic endoscope system |
Also Published As
Publication number | Publication date |
---|---|
JP2881498B2 (en) | 1999-04-12 |
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