JPS5839793B2 - Zinc oxide porcelain for high frequency sputtering - Google Patents
Zinc oxide porcelain for high frequency sputteringInfo
- Publication number
- JPS5839793B2 JPS5839793B2 JP52056860A JP5686077A JPS5839793B2 JP S5839793 B2 JPS5839793 B2 JP S5839793B2 JP 52056860 A JP52056860 A JP 52056860A JP 5686077 A JP5686077 A JP 5686077A JP S5839793 B2 JPS5839793 B2 JP S5839793B2
- Authority
- JP
- Japan
- Prior art keywords
- zinc oxide
- target
- density
- high frequency
- sputtering
- 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
Links
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 title claims description 30
- 238000004544 sputter deposition Methods 0.000 title claims description 20
- 239000011787 zinc oxide Substances 0.000 title claims description 15
- 229910052573 porcelain Inorganic materials 0.000 title claims description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 9
- 229910052802 copper Inorganic materials 0.000 claims description 9
- 239000010949 copper Substances 0.000 claims description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims description 9
- 239000011574 phosphorus Substances 0.000 claims description 9
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052748 manganese Inorganic materials 0.000 claims description 6
- 239000011572 manganese Substances 0.000 claims description 6
- 239000013078 crystal Substances 0.000 description 13
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 5
- 229910052786 argon Inorganic materials 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000007088 Archimedes method Methods 0.000 description 1
- -1 Cu3P Chemical compound 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 238000010574 gas phase reaction Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011656 manganese carbonate Substances 0.000 description 1
- 235000006748 manganese carbonate Nutrition 0.000 description 1
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940063666 oxygen 90 % Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005478 sputtering type Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Physical Vapour Deposition (AREA)
Description
【発明の詳細な説明】
この発明は高周波スパッタリングのターゲットに用いら
れる酸化亜鉛系磁器に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to zinc oxide ceramic used as a target for high frequency sputtering.
酸化亜鉛の圧電結晶膜の製造方法としては、真空蒸着法
、気相反応法あるいはスパッタリング法などがある。Methods for producing piezoelectric crystal films of zinc oxide include vacuum evaporation, gas phase reaction, and sputtering.
この中でスパッタリング法には直流2極型、直流3極型
および高周波スパッタリング法がある。Among these sputtering methods, there are two types of sputtering methods: a DC two-pole type, a DC three-pole type, and a high-frequency sputtering method.
直流2極型はスパッタリング法の中でもつとも単純であ
るが、ターゲットとなる酸化亜鉛磁器の比抵抗を低くし
ないと、イオンに曝されるターゲットの表面には正電荷
が蓄積されるため、スパッタリングが効率よく行えず、
安定な放電が維持できなかった。The DC bipolar type is one of the simplest sputtering methods, but unless the specific resistance of the zinc oxide porcelain target is lowered, positive charges will accumulate on the surface of the target exposed to ions, resulting in poor sputtering. I can't do it efficiently,
Stable discharge could not be maintained.
また比抵抗の低いターゲットを用いるため、得られた膜
の比抵抗も低くなる傾向がある。Furthermore, since a target with a low specific resistance is used, the specific resistance of the obtained film also tends to be low.
これらの膜は誘電体緩和現象により高い周波数での利用
は可能であるが、低い周波数領域に至る広い範囲での利
用ができなかった。Although these films can be used at high frequencies due to the dielectric relaxation phenomenon, they have not been able to be used over a wide range of low frequencies.
また、このようなスパッタリング法では一般に雰囲気ガ
スとして、酸素などの活性ガスやアルゴンなどの不活性
ガス、またはそれらを混合して用いている。Further, in such a sputtering method, an active gas such as oxygen, an inert gas such as argon, or a mixture thereof is generally used as the atmospheric gas.
結晶膜の比抵抗を高くする方法として、雰囲気ガス中の
酸素量を増す方法があるが、この場合結晶膜の成長速度
が遅くなるという欠点があった。One method of increasing the specific resistance of a crystal film is to increase the amount of oxygen in the atmospheric gas, but this method has the drawback of slowing down the growth rate of the crystal film.
これに対し、高周波スパッタリング法はターゲットに低
抵抗のものでも高抵抗のものでも用いることができると
いう利点があるが、結晶膜を工業的に量産するには膜の
成長速度を上げなげればならない。In contrast, the high-frequency sputtering method has the advantage of being able to use targets with either low or high resistance, but in order to industrially mass-produce crystalline films, it is necessary to increase the growth rate of the film. .
そのためにはターゲットとして高密度のものが要求され
る。For this purpose, a high-density target is required.
つまり、密度が高ければターゲットの単位面積当たりに
印加するパワー(パワー密度)を高くすることができ、
膜の成長速度が上がるからである。In other words, if the density is high, the power applied per unit area of the target (power density) can be increased.
This is because the growth rate of the film increases.
さらに、上記したように酸化亜鉛の圧電結晶膜を低周波
領域から高周波領域まで広い範囲で利用しようとすれば
、結晶膜の比抵抗を上げる必要があり、ターゲットとし
ては高抵抗のものが要求される。Furthermore, as mentioned above, if a piezoelectric crystal film of zinc oxide is to be used in a wide range from low frequency range to high frequency range, it is necessary to increase the specific resistance of the crystal film, and a target with high resistance is required. Ru.
従来はターゲットに高純度の酸化亜鉛の磁器を用いてい
たが、焼成前の成型品を1300’C以上の高温で焼成
すると、焼結密度は理論密度の90%以上になるが、比
抵抗は低くなり、高周波スパッタリング用のターゲット
としては不適当である。Conventionally, high-purity zinc oxide porcelain was used as a target, but when the pre-fired molded product is fired at a high temperature of 1300'C or higher, the sintered density becomes over 90% of the theoretical density, but the specific resistance decreases. This makes it unsuitable as a target for high frequency sputtering.
逆に1300℃未満で焼成すると比抵抗は高くなるが、
焼結密度は理論密度の80%に満たず、これもターゲッ
トとして不適当で、いずれの場合も高純度の酸化亜鉛磁
器では高抵抗で高密度のものは得られなかった。On the other hand, when fired at less than 1300℃, the specific resistance increases, but
The sintered density was less than 80% of the theoretical density, which was also inappropriate as a target, and in all cases, high resistance and high density could not be obtained with high purity zinc oxide porcelain.
たとえば、低密度のターゲット(焼結密度/理論密度X
100<90%)で高周波スパンタリングを行った場
合、得られた圧電結晶膜の表面は凹凸となる。For example, a low density target (sintered density/theoretical density
100<90%), the surface of the obtained piezoelectric crystal film becomes uneven.
これは酸化亜鉛クラスターが不均一に塊状になって飛ん
だことによるものと推察される。This is presumably due to the fact that the zinc oxide clusters were dispersed unevenly.
上記したような問題を種々検討した結果、酸化亜鉛にリ
ンと、マンガンまたは銅のうち1種あるいは2種を含有
させて得た磁器は比抵抗が高く、高密度でしかも磁器全
体にわたって密度分布差が少ないターゲットが得られる
ことを見い出したのである。As a result of various studies on the above-mentioned problems, we found that porcelain obtained by adding phosphorus to zinc oxide and one or two of manganese or copper has a high resistivity, a high density, and a difference in density distribution throughout the porcelain. They discovered that it is possible to obtain targets with a small number of targets.
以下この発明を実施例に従って詳述する。This invention will be described in detail below according to examples.
実施例
原料としてZnO、Zn3 (PO4)2.4H20、
MnCO3、CuOの各粉末を用い、第1表に示す比率
の磁器が得られるように調合して湿式、混合した。Examples of raw materials include ZnO, Zn3 (PO4)2.4H20,
MnCO3 and CuO powders were prepared and wet-mixed so as to obtain porcelain having the ratios shown in Table 1.
これらを脱水したのち600〜800℃で2時間仮焼を
行った。After dehydrating these, they were calcined at 600 to 800°C for 2 hours.
次に有機バインダとともに湿式ミルで粉砕、混合し、さ
らに脱水、乾燥したのち整粒した。Next, it was ground and mixed with an organic binder in a wet mill, further dehydrated, dried, and then sized.
こののち粉末を1000 kg/ Cr71.の圧力で
加圧し、直径100關、厚み5■の円板に成型した。After this, 1000 kg/Cr71. The mixture was pressurized at a pressure of 100 cm and molded into a disk with a diameter of 100 cm and a thickness of 5 cm.
さらに成型円板を1200℃で2時間焼**成して、リ
ンとマンガンまたは銅のうち1種あるいは2種を含むタ
ーゲット試料を作成した。Furthermore, the molded disk was baked at 1200° C. for 2 hours to create a target sample containing one or both of phosphorus, manganese, and copper.
なお、参考例である試料番号1〜4については第1表に
示す焼成条件で試料を作成した。Note that samples Nos. 1 to 4, which are reference examples, were prepared under the firing conditions shown in Table 1.
得られたターゲットの比抵抗、理論密度に対する焼結密
度の百分率(焼結密度/理論密度X100)を測定した
ところ、第1表に示すような結果が得られた。When the resistivity of the obtained target and the percentage of the sintered density with respect to the theoretical density (sintered density/theoretical density X100) were measured, the results shown in Table 1 were obtained.
ここで酸化亜鉛の理論密度は5.67P/cf?Lとし
た。Here, the theoretical density of zinc oxide is 5.67P/cf? It was set as L.
次にターゲットの密度分布を調べるため、第1図のよう
にターゲットの中心から0.10.20.30.40關
間隔に一辺約10X 10朋、厚さ3〜4關の正方形板
を切り出した。Next, in order to investigate the density distribution of the target, square plates of approximately 10 x 10 mm on each side and 3 to 4 mm thick were cut out at 0.10.20.30.40 square intervals from the center of the target, as shown in Figure 1. .
切り出した磁器の両面および周囲を研磨し、表面上に薄
いワックス層を付着させ、焼結密度の測定試料とした。Both sides and the surrounding area of the cut porcelain were polished, a thin wax layer was attached on the surface, and the sample was used as a measurement sample for sintered density.
密度の測定はへキサクロール=1・3−ブタジェン(2
0°Cでの密度1.682 P/i) ヲ浸漬液として
アルキメデス法により行った。The density was measured using hexachlor=1,3-butadiene (2
Density at 0°C: 1.682 P/i) The Archimedes method was used as an immersion liquid.
第2表は各測定位置での焼結密度およびその標準偏差(
σ)を示したものである。Table 2 shows the sintered density at each measurement position and its standard deviation (
σ).
第2表からこの発明によるものは焼結磁器の各位置にお
ける密度バラツキ、すなわちσが大幅に改善されている
ことがわかる。From Table 2, it can be seen that the density variation at each position of the sintered porcelain, that is, σ, is significantly improved in the case of the present invention.
次に上記したターゲットを用いて高周波スパッタリング
法により酸化亜鉛の圧電結晶膜を作成した。Next, a piezoelectric crystal film of zinc oxide was created by high-frequency sputtering using the target described above.
第2図は高周波スパッタリング法のうち高周波2極スパ
ツタリング法を実施するための装置を示す。FIG. 2 shows an apparatus for implementing a high frequency bipolar sputtering method among high frequency sputtering methods.
1は気密容器(ベルジャ)を示し、この気密容器1には
一対の平行平板状の陰極2と陽極3が配置されている。Reference numeral 1 denotes an airtight container (bell jar), and a pair of parallel plate-shaped cathode 2 and anode 3 are arranged in this airtight container 1.
陰極2の上には上記した各ターゲット試料4が固定され
る。Each target sample 4 described above is fixed on the cathode 2 .
5はシャッタである。陽極3には被着物となるガラス、
金属などの基板6が固定され、この基板6はスパッタリ
ング中で200〜500℃の範囲で加熱される。5 is a shutter. The anode 3 has glass as a deposit,
A substrate 6 made of metal or the like is fixed, and this substrate 6 is heated in the range of 200 to 500° C. during sputtering.
7は排気孔、8はガス導入口である。7 is an exhaust hole, and 8 is a gas inlet.
高周波スパッタリングをするには、気密容器1を密封し
たのち排気孔7からI X 10 ’ torr以上
の真空度になるように排気する。To perform high frequency sputtering, the airtight container 1 is sealed and then evacuated from the exhaust hole 7 to a degree of vacuum of I.times.10' torr or more.
次にガス導入口8からアルゴン、酸素あるいは酸素とア
ルゴンの混合ガスを導入し、ガス圧がlXl0 ”〜
1X 10−3t□rrになるようにする。Next, argon, oxygen, or a mixed gas of oxygen and argon is introduced from the gas inlet 8 until the gas pressure reaches lXl0''~
Make it 1X 10-3t□rr.
陰極2には高周波電源9により高周波電圧を印加する。A high frequency voltage is applied to the cathode 2 by a high frequency power source 9.
ターゲット試料4には単位面積当り2〜IOW/crr
tの高周波電力を供給する。2 to IOW/crr per unit area for target sample 4
t high frequency power is supplied.
酸化亜鉛の圧電結晶膜は実際に次のスパッタリング条件
により作成した。A piezoelectric crystal film of zinc oxide was actually created under the following sputtering conditions.
混合ガス比;アルゴン:酸素−90容量%:10容量%
圧力;2X10−3torr
高周波電源の周波数;13.56MHz
高周波電源の電カニ6W/cポ
被着面のガラス基板温度;350℃
上記した条件によりスパッタリングを行い、圧電結晶膜
の膜質を調べたところ第1表に示すような結果であった
。Mixed gas ratio: Argon: Oxygen - 90% by volume: 10% by volume Pressure: 2X10-3torr Frequency of high frequency power supply: 13.56MHz Temperature of the glass substrate on the surface to which electric crab 6W/c of high frequency power supply is adhered: 350°C The above conditions Sputtering was carried out using the method described above, and the film quality of the piezoelectric crystal film was examined, and the results were as shown in Table 1.
第1表からリンと、マンガンまたは銅のうち1種あるい
は2種を含有させることにより膜質の良好な圧電結晶膜
が得られている。From Table 1, piezoelectric crystal films with good film quality can be obtained by containing phosphorus and one or both of manganese and copper.
さらに、各ターゲット試料に印加できる最大入力電力と
焼結密度の関係を測定したところ第3図のような結果を
示した。Furthermore, when the relationship between the maximum input power that can be applied to each target sample and the sintered density was measured, the results shown in FIG. 3 were obtained.
なおターゲット試料は20個の平均値で、そのバラツキ
も第3図に示した。The average value of 20 target samples is shown in FIG. 3, and the variation thereof is also shown in FIG.
第3図からこの発明によるものは従来のものにくらべ最
大入力電力が2倍以上となり、結晶膜の形成速度を2倍
以上にすることができ、量産性を高めることができると
いう効果を有する。As can be seen from FIG. 3, the device according to the present invention has the effect that the maximum input power is more than twice that of the conventional device, the crystal film formation speed can be more than doubled, and mass productivity can be improved.
なお、この発明において酸化亜鉛にリンと、マンガンま
たは銅のうち1種あるいは2種を含有させる範囲は、リ
ン0.01〜20.0原子%、マンガンまたは銅はいず
れも0.01〜20.0原子%の範囲にあればよい。In the present invention, the range in which phosphorus and one or both of manganese and copper are contained in zinc oxide is 0.01 to 20.0 atomic % for phosphorus, and 0.01 to 20.0 atomic % for both manganese and copper. It is sufficient if it is in the range of 0 atomic %.
つまり、リンが0.01%原子%に満たなければ焼結密
度、比抵抗は大きくならず、20.0原子%を越えると
磁器粒子(グレイン)が大きく成長し、かえって低密度
、低抵抗のものになってしまう。In other words, if the phosphorus content is less than 0.01 atomic %, the sintered density and resistivity will not increase, and if it exceeds 20.0 atomic %, the porcelain grains will grow large, resulting in a low density and low resistance. It becomes something.
またマンガンまたは銅が0.01原子%未満では比抵抗
が上がらず、20.0原子%を越えると得られた結晶膜
の配向性が悪くなる。Further, if the amount of manganese or copper is less than 0.01 atomic %, the specific resistance will not increase, and if it exceeds 20.0 atomic %, the orientation of the obtained crystal film will be poor.
また、リン、マンガンおよび銅は単体もしくは酸化物な
どの化合物を添加物として用いても同様の効果が得られ
る。Furthermore, similar effects can be obtained by using phosphorus, manganese, and copper alone or in compounds such as oxides as additives.
またこの他に、たとえばリンと銅についてリンと銅の化
合物、たとえばCu3P、Cu2P2O7、Cu3(P
O4)2・3H20などとして含有させてもよい。In addition, for example, compounds of phosphorus and copper such as Cu3P, Cu2P2O7, Cu3(P
It may be contained as O4)2.3H20 or the like.
以上のようにこの発明によれば、従来のターゲットにく
らべ焼結密度が低く、高密度でその密度のバラツキが1
枚のターゲット内で小さなものが得られる。As described above, according to the present invention, the sintered density is lower than that of conventional targets, and the variation in density is reduced by 1 at high densities.
You can get something small within the target.
また最大入力電力の大きなものが得られ、しかも結晶膜
の品質の良いものが量産性よく得られるという効果を有
する。Further, it has the effect that a large maximum input power can be obtained, and a crystal film of good quality can be obtained with good mass production.
第1図はターゲット試料から焼結密度を測定するための
試料を切り出すための説明図、第2図は高周波2極スパ
ツタリング装置、第3図はターゲット試料に印加できる
最大入力電力と焼結密度の関係を示す図である。
1・・・・・・気密容器、2・・・・・・陰極、3・・
・・・・陽極、4・・・・・・ターゲット、6・・・・
・・基板。Figure 1 is an explanatory diagram for cutting out a sample for measuring sintered density from a target sample, Figure 2 is a high-frequency two-pole sputtering device, and Figure 3 is an illustration of the maximum input power that can be applied to the target sample and the sintered density. It is a figure showing a relationship. 1... Airtight container, 2... Cathode, 3...
...Anode, 4...Target, 6...
··substrate.
Claims (1)
酸化亜鉛にリンと、マンガンまたは銅のうち1種あるい
は2種を含有させたことを特徴とする高周波スパッタリ
ング用酸化亜鉛系磁器。1. As a target for high frequency sputtering,
Zinc oxide-based porcelain for high-frequency sputtering, characterized in that zinc oxide contains phosphorus and one or both of manganese and copper.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52056860A JPS5839793B2 (en) | 1977-05-16 | 1977-05-16 | Zinc oxide porcelain for high frequency sputtering |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52056860A JPS5839793B2 (en) | 1977-05-16 | 1977-05-16 | Zinc oxide porcelain for high frequency sputtering |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53141316A JPS53141316A (en) | 1978-12-09 |
| JPS5839793B2 true JPS5839793B2 (en) | 1983-09-01 |
Family
ID=13039159
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP52056860A Expired JPS5839793B2 (en) | 1977-05-16 | 1977-05-16 | Zinc oxide porcelain for high frequency sputtering |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5839793B2 (en) |
-
1977
- 1977-05-16 JP JP52056860A patent/JPS5839793B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS53141316A (en) | 1978-12-09 |
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