JP2812652B2 - Manufacturing method of waveguide type optical element - Google Patents
Manufacturing method of waveguide type optical elementInfo
- Publication number
- JP2812652B2 JP2812652B2 JP5273710A JP27371093A JP2812652B2 JP 2812652 B2 JP2812652 B2 JP 2812652B2 JP 5273710 A JP5273710 A JP 5273710A JP 27371093 A JP27371093 A JP 27371093A JP 2812652 B2 JP2812652 B2 JP 2812652B2
- Authority
- JP
- Japan
- Prior art keywords
- buffer layer
- optical
- oxygen
- heat treatment
- waveguide
- 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.)
- Expired - Fee Related
Links
- 230000003287 optical effect Effects 0.000 title claims description 48
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000007789 gas Substances 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 23
- 238000010438 heat treatment Methods 0.000 claims description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 16
- 239000001301 oxygen Substances 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- 239000000758 substrate Substances 0.000 claims description 15
- 238000009792 diffusion process Methods 0.000 claims description 14
- 239000010936 titanium Substances 0.000 claims description 11
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 7
- GQYHUHYESMUTHG-UHFFFAOYSA-N lithium niobate Chemical compound [Li+].[O-][Nb](=O)=O GQYHUHYESMUTHG-UHFFFAOYSA-N 0.000 claims description 7
- 229910052719 titanium Inorganic materials 0.000 claims description 7
- 238000000151 deposition Methods 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 2
- 238000005259 measurement Methods 0.000 description 16
- 238000007796 conventional method Methods 0.000 description 15
- 229910013641 LiNbO 3 Inorganic materials 0.000 description 10
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 8
- 229910001882 dioxygen Inorganic materials 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 238000004544 sputter deposition Methods 0.000 description 5
- 238000001771 vacuum deposition Methods 0.000 description 5
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 238000005229 chemical vapour deposition Methods 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000005587 bubbling Effects 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 230000001902 propagating effect Effects 0.000 description 2
- 238000007736 thin film deposition technique Methods 0.000 description 2
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000010365 information processing Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- -1 oxygen gas Chemical compound 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F2203/00—Function characteristic
- G02F2203/21—Thermal instability, i.e. DC drift, of an optical modulator; Arrangements or methods for the reduction thereof
Landscapes
- Optical Integrated Circuits (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明は、光通信分野・光情
報処理分野・光応用計測分野等で用いられる導波路型光
素子、とりわけ高速光変調器・高速光スイッチ等の導波
路型電気光学素子の製造方法に関するものである。本発
明方法により製造された導波路型光素子は、制御用直流
電圧を印加した場合においても安定した動作特性を示す
という特徴を有する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a waveguide type optical element used in the fields of optical communication, optical information processing, optical applied measurement, etc., and more particularly to a waveguide type electro-optic such as a high speed optical modulator and a high speed optical switch. The present invention relates to a method for manufacturing an element. The waveguide type optical device manufactured by the method of the present invention has a feature that it exhibits stable operation characteristics even when a control DC voltage is applied.
【0002】[0002]
【従来の技術】本発明に関わる従来技術の例として、ニ
オブ酸リチウム基板を用いたマッハツェンダ型光変調器
をとりあげ、これについて説明する。この光素子は、ニ
オブ酸リチウム(LiNbO3)基板上に、Ti熱拡散法
により、Y分岐・合波の形態をもつ導波路パタンを形成
し、その上に誘電体材料よりなるバッファ層を形成し、
さらにその上に導波路パタンに対応する電極を配設した
ものである(例えば、西原、春名、栖原 共著「光集積
回路」、オーム社、1985) 。必要に応じ、光素子使
用環境温度が変化した場合にLiNbO3 の焦電効果に
より発生する電荷を、電極下部分に集中させることなく
素子表面に均一分散させ、温度変化に基づく素子特性
(変調位相)のドリフトを低減させる目的で、バッファ
層に比べ低い電気抵抗を有する薄層を、バッファ層の
上、あるいは下に挿入することもある(K.Seino, T. Na
kazawa, Y. Kubota, M. Doi, T. Yamane and H.Hakogi;
Proc. OFC' 92,San Jose, Feb.8−11,1992
(Optical Soc. Am., Washington, 1992) pp.32
5、十文字、野沢;電子情報通信学会論文誌C−1,J
75−C(1992)17、特開平5−66428等)
。2. Description of the Related Art As an example of the prior art relating to the present invention, a Mach-Zehnder type optical modulator using a lithium niobate substrate will be described and described. In this optical device, a waveguide pattern having a Y-branch / combination form is formed on a lithium niobate (LiNbO 3 ) substrate by a Ti thermal diffusion method, and a buffer layer made of a dielectric material is formed thereon. And
Further, an electrode corresponding to the waveguide pattern is provided thereon (for example, "Optical Integrated Circuit", co-authored by Nishihara, Haruna, and Suhara, Ohmsha, 1985). If necessary, the charge generated by the pyroelectric effect of LiNbO 3 when the ambient temperature of the optical device is changed is uniformly dispersed on the device surface without concentrating on the lower portion of the electrode, and the device characteristics (modulation phase ), A thin layer having a lower electric resistance than the buffer layer may be inserted above or below the buffer layer (K. Seino, T. Na
kazawa, Y. Kubota, M. Doi, T. Yamane and H. Hakogi;
Proc. OFC'92, San Jose, Feb. 8-11, 1992
(Optical Soc. Am., Washington, 1992) pp.32
5, cross letters, Nozawa; IEICE Transactions C-1, J
75-C (1992) 17, JP-A-5-66428, etc.)
.
【0003】光導波路をニオブ酸リチウム基板中に形成
するためのチタンの熱拡散処理は、1000℃前後の温
度で行われ、高温下におけるリチウムの外拡散(蒸発)
を抑制するために、湿潤ガス、つまり水中をバブリング
させたガス雰囲気を用いることが一般に行われている
(例えば、西原、春名、栖原 共著「光集積回路」、オ
ーム社、1985)。このような熱拡散雰囲気を形成す
るガスとしては、純酸素、アルゴン/酸素混合ガス、又
は空気等が用いられることが多い。[0003] Thermal diffusion treatment of titanium for forming an optical waveguide in a lithium niobate substrate is performed at a temperature of about 1000 ° C, and external diffusion (evaporation) of lithium at a high temperature.
It is common practice to use a humid gas, that is, a gas atmosphere in which water is bubbled, in order to suppress the occurrence of light (for example, Nishihara, Haruna, and Suhara, “Optical Integrated Circuit”, Ohmsha, 1985). As a gas for forming such a thermal diffusion atmosphere, pure oxygen, an argon / oxygen mixed gas, air, or the like is often used.
【0004】上記光素子の重要な構成要素である誘電体
バッファ層としては、一般にSiO2 あるいはAl2 O
3 の酸化物誘電体が用いられ、真空蒸着法、イオンアシ
スト真空蒸着法、スパッタリング法、又は化学的気相蒸
着法(CVD)などの汎用的な薄膜堆積方法を用いて導
波路を予め配設した基板上に形成される。The dielectric buffer layer, which is an important component of the optical device, is generally made of SiO 2 or Al 2 O.
Oxide dielectric 3 is used, a vacuum deposition method, ion-assisted vacuum deposition, sputtering, or pre-arranged in the waveguide using a chemical vapor deposition a generic thin film deposition method such as (CVD) Formed on the substrate.
【0005】SiO2 ,Al2 O3 などの酸化物は、高
い電気的絶縁性を有するとともに、誘電率(屈折率)が
小さいため、導波路中を伝播する光信号および電極中を
伝播する高周波電気信号が、これらの物質中に散乱して
損失することが少なく、また、基板(LiNbO3)物質
と同じ酸化物であるため、両層の界面における化学的結
合が強く、つまり付着強度が高いという、多くの利点を
備えたバッファ層を形成することができる。Oxides such as SiO 2 and Al 2 O 3 have high electrical insulation and a small dielectric constant (refractive index), so that an optical signal propagating in a waveguide and a high-frequency signal propagating in an electrode are used. Since the electric signal is less likely to be scattered and lost in these substances and is the same oxide as the substrate (LiNbO 3 ) substance, the chemical bonding at the interface between both layers is strong, that is, the adhesion strength is high. That is, a buffer layer having many advantages can be formed.
【0006】上記誘電体バッファ層膜を、上述の真空蒸
着法、又はスパッタリング法などの方法で形成した後、
膜中の酸素欠損を補うために、600℃程度の酸化雰囲
気中で熱処理を行う(特開昭58−181318号)こ
とが知られている。このとき、リチウムの外拡散(蒸
発)を抑制するため、および膜の酸化反応を促進するた
めに、湿潤酸素ガス、例えば水中をバブリングさせた酸
素ガスを用いるのが一般的である。After the dielectric buffer layer film is formed by the above-described method such as the vacuum evaporation method or the sputtering method,
It is known that heat treatment is performed in an oxidizing atmosphere at about 600 ° C. to compensate for oxygen deficiency in the film (Japanese Patent Application Laid-Open No. 58-181318). At this time, in order to suppress the outward diffusion (evaporation) of lithium and to promote the oxidation reaction of the film, it is general to use a wet oxygen gas, for example, an oxygen gas obtained by bubbling water.
【0007】[0007]
【発明が解決しようとする課題】従来方法において導波
路形成時の熱拡散およびバッファ層の熱処理を、上述の
ように湿潤ガス中で行うのが一般的であったが、このよ
うな従来方法には、光素子特性、特にニオブ酸リチウム
基板を用いたマッハツェンダ型光変調器で問題とされて
いるDC−ドリフト現象などにおいて解決すべき問題が
ある。In the conventional method, the thermal diffusion at the time of forming the waveguide and the heat treatment of the buffer layer are generally performed in a wet gas as described above. There is a problem to be solved in the characteristics of optical elements, especially in a DC-drift phenomenon which is a problem in a Mach-Zehnder type optical modulator using a lithium niobate substrate.
【0008】DC−ドリフト現象とは、光素子において
直流電圧により調整された光変調位相が経時的に変化
し、調整点からずれてしまう現象である。このDC−ド
リフトの原因については、いまだ種々の議論がなされて
いる段階であるが、基板とバッファ層の電気的物性(抵
抗率・誘電率等)に強く関係しているという見方が有力
であり、これを完全に防止することは困難である。(十
文字、野沢;電子情報通信学会論文誌C−1,J75−
C−1(1992)17、特開平5−66428号、特
開平4−346310号等)。本発明は、従来方法の上
記問題点を解消し、得られる光素子の特性を改善し、特
にDC−ドリフト現象が著く少ない導波路型光素子を効
率よく製造する方法を提供しようとするものである。[0008] The DC-drift phenomenon is a phenomenon in which an optical modulation phase adjusted by a DC voltage in an optical element changes with time and deviates from an adjustment point. Although the cause of this DC-drift is still being discussed at various stages, the view that it is strongly related to the electrical properties (resistivity, dielectric constant, etc.) of the substrate and the buffer layer is influential. It is difficult to completely prevent this. (Tomoji, Nozawa; IEICE Transactions C-1, J75-
C-1 (1992) 17, JP-A-5-66428, JP-A-4-346310, and the like. An object of the present invention is to solve the above-mentioned problems of the conventional method, improve the characteristics of the obtained optical device, and particularly provide a method of efficiently manufacturing a waveguide type optical device having a remarkably small DC-drift phenomenon. It is.
【0009】[0009]
【課題を解決するための手段】本発明に係る導波路型光
素子の製造方法は、ニオブ酸リチウム基板上にチタンを
熱拡散させて所望形状の光導波路を形成する工程と、こ
の光導波路の直上に誘電体バッファ層を堆積形成する工
程と、この誘電体バッファ層の上に電極を配設する工程
とを含み、前記光導波路形成のためのチタン熱拡散工程
を、少なくとも酸素を含有し0℃以下の露点を有する乾
燥ガス雰囲気内において行い、かつ前記誘電体バッファ
層に、少なくとも酸素を含有し0℃以下の露点を有する
乾燥ガス雰囲気内において熱処理を施す、ことを特徴と
するものである。本発明方法において、前記誘電体バッ
ファ層の熱処理は約600℃の温度において行われるこ
とが好ましい。また本発明方法において、前記チタン熱
拡散工程及び前記誘電体バッファ層の熱処理における乾
燥ガスの各々が−70℃以下の露点を示す。According to the present invention, there is provided a method of manufacturing a waveguide type optical device, comprising the steps of thermally diffusing titanium on a lithium niobate substrate to form an optical waveguide having a desired shape; A step of depositing and forming a dielectric buffer layer immediately above, and a step of arranging an electrode on the dielectric buffer layer. Performing in a dry gas atmosphere having a dew point of not more than 0 ° C., and subjecting the dielectric buffer layer to heat treatment in a dry gas atmosphere containing at least oxygen and having a dew point of 0 ° C. or less. . In the method of the present invention, the heat treatment of the dielectric buffer layer is preferably performed at a temperature of about 600 ° C. In the method of the present invention, each of the drying gases in the titanium thermal diffusion step and the heat treatment of the dielectric buffer layer has a dew point of -70 ° C or less.
【0010】[0010]
【発明の実施の形態】本発明方法において、ニオブ酸リ
チウム(LiNbO3)からなる基板上にチタンを所定形
状に熱拡散させて光導波路が形成される。この熱拡散工
程は、少なくとも酸素を含有する乾燥ガス雰囲気中にお
いて行われ、その熱拡散温度は900〜1000℃であ
ることが好ましい。この酸素含有乾燥ガスとしては、酸
素ガス、アルゴン/酸素混合ガス、又は空気などの少な
くとも酸素を含有するガスを用いることが好ましいが一
般には酸素ガスを用いることがより好ましい。この乾燥
ガス雰囲気中の水蒸気含有量は、当該ガスが0℃以下の
露点を示す量であることが好ましいがこの露点が−70
℃以下であることがより好ましい。DESCRIPTION OF THE PREFERRED EMBODIMENTS In the method of the present invention, an optical waveguide is formed by thermally diffusing titanium into a predetermined shape on a substrate made of lithium niobate (LiNbO 3 ). This heat diffusion step is performed in a dry gas atmosphere containing at least oxygen, and the heat diffusion temperature is preferably 900 to 1000 ° C. As the oxygen-containing dry gas, it is preferable to use a gas containing at least oxygen such as oxygen gas, an argon / oxygen mixed gas, or air, but generally it is more preferable to use oxygen gas. The water vapor content in the dry gas atmosphere is preferably such that the gas exhibits a dew point of 0 ° C. or less, but the dew point is −70.
It is more preferable that the temperature is not higher than ° C.
【0011】上述のようにして形成された光導波路の直
上に、誘電体バッファ層を形成する。この誘電体バッフ
ァ層は、SiO2 ,Al2 O3 、又はITOなどの誘電
体酸化物を、真空蒸着法、イオンアシスト真空蒸着法、
スパッタリング法、又は化学的気相蒸着法(CVD)な
どの薄膜堆積形成法により堆積させて形成される。この
ようにして形成された誘電体バッファ層に、少なくとも
酸素を含有する乾燥ガス雰囲気内において熱処理を施
す。その熱処理温度は約600℃前後であることが好ま
しい。前記雰囲気ガスとしては、酸素ガス、アルゴン/
酸素混合ガス、又は空気などの酸素含有乾燥ガスを用い
ることが好ましく、特に酸素ガスを用いることが好まし
い。この熱処理雰囲気乾燥ガスの水分含有量は、0℃以
下のガス露点を示す量であることが好ましくこの露点は
−70℃以下であることがより好ましい。[0011] A dielectric buffer layer is formed immediately above the optical waveguide formed as described above. This dielectric buffer layer is formed by depositing a dielectric oxide such as SiO 2 , Al 2 O 3 , or ITO by a vacuum deposition method, an ion-assisted vacuum deposition method,
It is formed by deposition by a thin film deposition method such as a sputtering method or a chemical vapor deposition method (CVD). The dielectric buffer layer thus formed is subjected to a heat treatment in a dry gas atmosphere containing at least oxygen. The heat treatment temperature is preferably about 600 ° C. As the atmosphere gas, oxygen gas, argon /
It is preferable to use an oxygen-containing gas or an oxygen-containing dry gas such as air, and it is particularly preferable to use an oxygen gas. The moisture content of the dry gas in the heat treatment atmosphere is preferably an amount showing a gas dew point of 0 ° C. or less, and more preferably the dew point is −70 ° C. or less.
【0012】本発明方法において誘電体バッファ層の上
に、前記光導波路を通る光波の特性を調整するための電
極が配設される。この電極の配設は、フォトリソグラフ
技術と薄膜成形技術とを用いてAu電極パターン(厚
さ:数百mm)を作製したのち、金メッキ技術を用いて電
極パターンの肉厚を数μm程度に肉付けすることによっ
て行われる。In the method of the present invention, an electrode for adjusting characteristics of a light wave passing through the optical waveguide is provided on the dielectric buffer layer. This electrode is provided by forming an Au electrode pattern (thickness: several hundred mm) using photolithography technology and thin film forming technology, and then increasing the thickness of the electrode pattern to approximately several μm using gold plating technology. It is done by doing.
【0013】本発明方法により得られた光素子の特性
を、従来方法により得られた光素子と対比して説明す
る。図1に、従来法により作成したTi:LiNbO3
マッハツェンダ型光強度変調器の、DC−ドリフト測定
結果を示す(2サンプルについて測定した結果を表
示)。Ti拡散導波路の作成は、980℃で、湿潤合成
空気(室温の超純水中をバブリング、水分含有量:炉内
に導入されるガスが40℃の最終露点を示す量)中を流
しながら行った。その上に酸化シリコンよりなるバッフ
ァ層をスパッタリング法により堆積形成し、600℃、
湿潤酸素気流中で熱処理した。得られた光導波路のDC
−ドリフトの測定は、光導波路に、80℃においてDC
バイアス電圧5Vを印加し、さらにAC電圧(±10
V)を重畳させて印加し、光素子から出力される光変調
波形をオシロスコープ上で観察しながら、任意の光強度
ピーク位置の経時シフトを追尾することにより行った。
DC−ドリフトは温度加速される現象であり、本図に示
す80℃の測定結果は、室温(25℃)測定に比べ、ド
リフト速度がおよそ1000倍に加速されて観測され
る。図1から明らかなように、従来法により作成した光
変調器では、数時間程度で、印加したバイアス(5V)
に相当するドリフトが観測された。The characteristics of the optical device obtained by the method of the present invention will be described in comparison with the optical device obtained by the conventional method. FIG. 1 shows Ti: LiNbO 3 prepared by a conventional method.
3 shows the results of DC-drift measurement of a Mach-Zehnder type optical intensity modulator (the results of measurements on two samples are shown). The preparation of the Ti diffusion waveguide is performed at 980 ° C. while flowing in wet synthetic air (bubbling in ultrapure water at room temperature, water content: the amount of gas introduced into the furnace indicating the final dew point of 40 ° C.). went. A buffer layer made of silicon oxide is deposited and formed thereon by a sputtering method.
Heat treatment was performed in a stream of moist oxygen. DC of the obtained optical waveguide
-Drift measurement is performed by applying a DC
A bias voltage of 5 V is applied, and an AC voltage (± 10
V) was superimposed and applied, and by observing the optical modulation waveform output from the optical element on an oscilloscope, tracking of a temporal shift of an arbitrary light intensity peak position was performed.
The DC-drift is a phenomenon in which the temperature is accelerated, and the measurement result at 80 ° C. shown in this figure is observed with the drift speed accelerated by about 1000 times compared to the measurement at room temperature (25 ° C.). As is clear from FIG. 1, in the optical modulator manufactured by the conventional method, the applied bias (5 V) was applied for about several hours.
Was observed.
【0014】一方、比較のために、上記の製造工程のう
ち、導波路の熱拡散処理を乾燥酸素(水分含有量:−7
0℃のガス露点を示す量)中で行い、バッファ層熱処理
を湿潤酸素気流中で行ったサンプルでは、図2に示すよ
うに、同一測定条件(バイアス電圧5V、測定温度80
℃)下のドリフト測定において、2〜3Vのドリフトし
か示さなかった(図1に対応する変調器の半分の値)。On the other hand, for comparison, in the above-mentioned manufacturing process, the thermal diffusion treatment of the waveguide was performed by using dry oxygen (water content: -7
As shown in FIG. 2, in the sample subjected to the buffer layer heat treatment in a wet oxygen stream, the same measurement conditions (a bias voltage of 5 V and a measurement temperature of 80 ° C.) were used.
C.) showed only a drift of 2-3 V (half the value of the modulator corresponding to FIG. 1).
【0015】また、上記方法においてバッファ層の熱処
理も乾燥酸素雰囲気中で行った例(実施例1)を図3に
示す。図3から明らかなように、熱処理雰囲気を湿潤ガ
スから乾燥ガス(水分含有量:−70℃のガス露点を示
す量)に変えたことにより、DC−ドリフトが一層改善
された。複数の異なるLiNbO3 基板(いずれもzカ
ット)を用いて行った測定においても、図2と同様の、
従来法の半分のドリフトしか観測されず、従って本発明
による処理方法が、少なくともLiNbO3 をベースと
する電気光学素子のDC−ドリフトを著しく改善するこ
とは明らかである。また、LiNbO3 と結晶構造を同
じくする他の電気光学結晶(例えばLiTaO3)につい
ても、同様な効果が得られることは、容易に類推でき
る。FIG. 3 shows an example (Example 1) in which the buffer layer is also heat-treated in a dry oxygen atmosphere in the above method. As is clear from FIG. 3, the DC-drift was further improved by changing the heat treatment atmosphere from a wet gas to a dry gas (water content: an amount indicating a gas dew point at −70 ° C.). In the measurement performed using a plurality of different LiNbO 3 substrates (all of which are z-cut), the same as in FIG.
It is clear that only half the drift of the conventional method is observed, so that the processing method according to the invention significantly improves the DC-drift of at least LiNbO 3 -based electro-optical elements. It can be easily analogized that the same effect can be obtained with another electro-optical crystal (for example, LiTaO 3 ) having the same crystal structure as LiNbO 3 .
【0016】上述したように、本発明の効果に関するメ
カニズムは、未だ明らかでないが、関連する実験結果と
して、熱処理雰囲気を用いることにより光素子チップ中
の水素含有量が変化することがわかっている(例えば、
L. Kovacs, M. Wohlecke, A.Jovanovic, K.Polgar and
S. Kapphan,“Infrared Absorption Study of the OH
Vibrational Band in LiNbO3 Crystal, " J. Phys. Che
m. Solids Vol.52(1991)pp. 797〜803に
数多くの研究結果が解説されている)。前述の文献と同
様なフーリエ変換赤外(IR)吸収スペクトル法により
実際に測定した、熱処理雰囲気の違いによる水素量の相
対変化を、OH伸縮モードの吸収係数値として、表1に
示す。以下の記述では、表1にならって、サンプル名を
“WET/WET”(従来法)、WET/DRT(従来
法)、“DRY/WET”(従来法)、“DRY/DR
Y”(本発明方法)のように呼ぶことにする。As described above, the mechanism relating to the effect of the present invention is not yet clear, but it has been found from a related experimental result that the hydrogen content in the optical element chip changes by using a heat treatment atmosphere ( For example,
L. Kovacs, M. Wohlecke, A. Jovanovic, K. Polgar and
S. Kapphan, “Infrared Absorption Study of the OH
Vibrational Band in LiNbO 3 Crystal , "J. Phys. Che
m. Solids Vol. 52 (1991) pp. 797-803 describes many research results). Table 1 shows the relative change in the amount of hydrogen due to the difference in the heat treatment atmosphere actually measured by the Fourier transform infrared (IR) absorption spectrum method similar to the above-mentioned literature, as the absorption coefficient value in the OH stretching mode. In the following description, according to Table 1, the sample names are “WET / WET” (conventional method), WET / DRT (conventional method), “DRY / WET” (conventional method), and “DRY / DR”.
Y "(the method of the present invention).
【0017】[0017]
【表1】 [Table 1]
【0018】表1からも明らかなように、本発明方法に
係る“DRY/DRY”サンプルでは、従来法に比べ、
チップ中の水素量(OH量)が著しく減少しており、こ
の現象はDC−ドリフトの減少に大きく寄与していると
考えられる。As is clear from Table 1, the "DRY / DRY" sample according to the method of the present invention has a smaller size than the conventional method.
The amount of hydrogen (OH) in the chip has been significantly reduced, and this phenomenon is considered to have greatly contributed to the reduction of DC-drift.
【0019】[0019]
【実施例】本発明を下記実施例により更に説明する。実施例1 乾燥酸素気流(水含有量:−70℃のガス露
点を示す量、温度:980℃)中で作成したZカットT
i:LiNbO3 導波路基板上に、SiO2 バッファ層
をスパッタリング法により形成し、乾燥酸素(露点:−
70℃)中で熱処理(600℃)する工程を経たマッハ
ツェンダ型光変調器(“DRY/DRY”サンプル)
の、DC−ドリフト測定結果を図3に示す。ドリフトの
測定条件は前述した条件と全く同じである。実施例1に
おけるDC−ドリフトは従来法(図1)のそれの約半分
に低下していた。The present invention is further described by the following examples. Example 1 Z-cut T prepared in a dry oxygen gas stream (water content: amount indicating a gas dew point of -70 ° C., temperature: 980 ° C.)
i: An SiO 2 buffer layer was formed on a LiNbO 3 waveguide substrate by a sputtering method, and dried oxygen (dew point: −
Mach-Zehnder type optical modulator (“DRY / DRY” sample) that has undergone a heat treatment (600 ° C.) in 70 ° C.)
FIG. 3 shows the results of the DC-drift measurement. The conditions for measuring the drift are exactly the same as those described above. The DC-drift in Example 1 was reduced to about half that of the conventional method (FIG. 1).
【0020】比較例1および実施例2 本発明の結果の
再現性を確認するために、図2,3で用いたZカットL
iNbO3 基板と製造メーカの異なる基板を用い、マッ
ハツェンダ型変調器を作成した。Ti熱拡散雰囲気、お
よびバッファ層熱処理雰囲気を変化させて、“DRY/
WET”(比較例1),“DRY/DRY”(実施例
2)サンプルを作成した。それぞれのDC−ドリフト測
定結果を図4(“DRY/WET”、比較例1)、図5
(“DRY/DRY”、実施例2)に示す。いずれもD
C−ドリフトが従来法(図1、基板のメーカは本実施例
と同じ)の約半分に低下しており、発明の再現性も確認
できた。 Comparative Example 1 and Example 2 In order to confirm the reproducibility of the results of the present invention, the Z-cut L used in FIGS.
A Mach-Zehnder modulator was manufactured using an iNbO 3 substrate and a substrate manufactured by a different manufacturer. By changing the Ti thermal diffusion atmosphere and the buffer layer heat treatment atmosphere, "DRY /
Wet "(Comparative Example 1) and" DRY / DRY "(Example 2) samples were prepared. The DC-drift measurement results are shown in FIG. 4 (" DRY / WET ", Comparative Example 1) and FIG.
("DRY / DRY", Example 2). Both are D
The C-drift was reduced to about half of the conventional method (FIG. 1, the substrate maker is the same as that of the present embodiment), and the reproducibility of the invention was confirmed.
【0021】[0021]
【発明の効果】本発明の工程により、導波路型電気光学
素子を高速光通信等に応用する上で問題となる、DC−
ドリフトの著しく低下した光素子を効率よく製造するこ
とが可能になった。According to the process of the present invention, there is a problem that DC-DC becomes a problem in applying the waveguide type electro-optical element to high-speed optical communication or the like.
It has become possible to efficiently manufacture an optical element with significantly reduced drift.
【図1】図1は、従来方法により製造されたTi−Li
NbO3 光変調器の一例のDC−ドリフト測定結果を示
すグラフ。BRIEF DESCRIPTION OF DRAWINGS FIG. 1 is a diagram showing a Ti-Li manufactured by a conventional method.
9 is a graph showing DC-drift measurement results of an example of the NbO 3 optical modulator.
【図2】図2は、従来方法により製造されたTi−Li
NbO3 光変調器の一例のDC−ドリフト測定結果を示
すグラフ。FIG. 2 is a diagram showing a Ti—Li manufactured by a conventional method.
9 is a graph showing DC-drift measurement results of an example of the NbO 3 optical modulator.
【図3】図3は、本発明方法により製造されたTi−L
iNbO3 光変調器の他の例のDC−ドリフト測定結果
を示すグラフ。FIG. 3 shows Ti-L produced by the method of the present invention.
9 is a graph showing DC-drift measurement results of another example of the iNbO 3 optical modulator.
【図4】図4は、従来方法により製造されたTi−Li
NbO3 光変調器のさらに他の例のDC−ドリフト測定
結果を示すグラフ。FIG. 4 is a diagram showing Ti—Li manufactured by a conventional method.
9 is a graph showing DC-drift measurement results of still another example of the NbO 3 optical modulator.
【図5】図5は、本発明方法により製造されたTi−L
iNbO3 光変調器のさらに他の例のDC−ドリフト測
定結果を示すグラフ。FIG. 5 shows Ti-L manufactured by the method of the present invention.
9 is a graph showing DC-drift measurement results of still another example of the iNbO 3 optical modulator.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 本田 秀紀 千葉県船橋市豊富町585番地 住友セメ ント株式会社 中央研究所内 (72)発明者 小林 正信 千葉県船橋市豊富町585番地 住友セメ ント株式会社 光電子事業部内 (72)発明者 木内 和昌 千葉県船橋市豊富町585番地 住友セメ ント株式会社 中央研究所内 (56)参考文献 特開 平6−347839(JP,A) 特開 平6−43412(JP,A) 特開 平4−249215(JP,A) 特開 平3−259204(JP,A) 特開 平2−196213(JP,A) (58)調査した分野(Int.Cl.6,DB名) G02F 1/00 - 1/055 505 G02B 6/12 - 6/14 G02F 1/29 - 1/313──────────────────────────────────────────────────続 き Continued on the front page (72) Inventor Hideki Honda 585 Tomicho, Funabashi-shi, Chiba Sumitomo Cement Co., Ltd.Sumitomo Central Research Institute (72) Inventor Masanobu Kobayashi 585, Tomiyoshi-cho, Funabashi-shi, Chiba Sumitomo Cement Co., Ltd. Within the Optoelectronics Division (72) Inventor Kazumasa Kiuchi 585 Toyotomi-cho, Funabashi-shi, Chiba Sumitomo Cement Co., Ltd. Central Research Laboratory (56) References JP, A) JP-A-4-249215 (JP, A) JP-A-3-259204 (JP, A) JP-A-2-196213 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) G02F 1/00-1/055 505 G02B 6/12-6/14 G02F 1/29-1/313
Claims (3)
散させて所望形状の光導波路を形成する工程と、この光
導波路の直上に誘電体バッファ層を堆積形成する工程
と、この誘電体バッファ層の上に電極を配設する工程と
を含み、 前記光導波路形成のためのチタン熱拡散工程を、少なく
とも酸素を含有し、0℃以下の露点を有する乾燥ガス雰
囲気内において行い、かつ前記誘電体バッファ層に、少
なくとも酸素を含有し、0℃以下の露点を有する乾燥ガ
ス雰囲気内において熱処理を施す、ことを特徴とする導
波路型光素子の製造方法。A step of thermally diffusing titanium on a lithium niobate substrate to form an optical waveguide having a desired shape; a step of depositing and forming a dielectric buffer layer immediately above the optical waveguide; Disposing a titanium heat diffusion step for forming the optical waveguide in an atmosphere of a dry gas containing at least oxygen and having a dew point of 0 ° C. or less, and A method for manufacturing a waveguide-type optical element, comprising: performing a heat treatment in a dry gas atmosphere containing at least oxygen and having a dew point of 0 ° C. or less in a buffer layer.
0℃の温度において行われる、請求項1に記載の方法。2. A heat treatment of the dielectric buffer layer is performed for about 60 hours.
The method according to claim 1, which is performed at a temperature of 0 ° C.
ッファ層の熱処理における乾燥ガスの各々が−70℃以
下の露点を有する、請求項1に記載の方法。3. The method of claim 1, wherein each of the drying gas in the titanium thermal diffusion step and the heat treatment of the dielectric buffer layer has a dew point of −70 ° C. or less.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5273710A JP2812652B2 (en) | 1993-11-01 | 1993-11-01 | Manufacturing method of waveguide type optical element |
| CA002133300A CA2133300C (en) | 1993-11-01 | 1994-09-29 | Optical waveguide device |
| EP94307165A EP0652457B1 (en) | 1993-11-01 | 1994-09-30 | Optical waveguide device |
| US08/315,981 US5526448A (en) | 1993-11-01 | 1994-09-30 | Optical waveguide modulator having a reduced D.C. drift |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5273710A JP2812652B2 (en) | 1993-11-01 | 1993-11-01 | Manufacturing method of waveguide type optical element |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH07128624A JPH07128624A (en) | 1995-05-19 |
| JP2812652B2 true JP2812652B2 (en) | 1998-10-22 |
Family
ID=17531482
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5273710A Expired - Fee Related JP2812652B2 (en) | 1993-11-01 | 1993-11-01 | Manufacturing method of waveguide type optical element |
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| Country | Link |
|---|---|
| JP (1) | JP2812652B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002090702A (en) | 2000-09-18 | 2002-03-27 | Sumitomo Osaka Cement Co Ltd | Waveguide type optical modulator and its manufacturing method |
| JP4665162B2 (en) | 2005-03-04 | 2011-04-06 | 住友大阪セメント株式会社 | Optical element and manufacturing method thereof |
| WO2013012023A1 (en) | 2011-07-19 | 2013-01-24 | 住友大阪セメント株式会社 | Optical waveguide element and method of manufacturing same |
| JP7069966B2 (en) * | 2018-03-29 | 2022-05-18 | 住友大阪セメント株式会社 | Optical control element |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02196213A (en) * | 1989-01-25 | 1990-08-02 | Oki Electric Ind Co Ltd | Formation of buffer layer of waveguide type element |
| JPH03259204A (en) * | 1990-03-09 | 1991-11-19 | Fujikura Ltd | Optical wavegiide substrate by diffusion of material for increasing refractive index |
| JP3213619B2 (en) * | 1991-02-05 | 2001-10-02 | パイオニア株式会社 | Method for manufacturing optical waveguide device and optical waveguide device |
| JPH0643412A (en) * | 1992-05-29 | 1994-02-18 | Kyocera Corp | Production of optical control device |
| JPH06347839A (en) * | 1993-06-08 | 1994-12-22 | Nec Corp | Optical control device |
-
1993
- 1993-11-01 JP JP5273710A patent/JP2812652B2/en not_active Expired - Fee Related
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