WO2017135294A1 - 多結晶誘電体薄膜および容量素子 - Google Patents
多結晶誘電体薄膜および容量素子 Download PDFInfo
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- WO2017135294A1 WO2017135294A1 PCT/JP2017/003577 JP2017003577W WO2017135294A1 WO 2017135294 A1 WO2017135294 A1 WO 2017135294A1 JP 2017003577 W JP2017003577 W JP 2017003577W WO 2017135294 A1 WO2017135294 A1 WO 2017135294A1
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- thin film
- dielectric thin
- polycrystalline dielectric
- polycrystalline
- film
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- 239000010409 thin film Substances 0.000 title claims abstract description 85
- 239000003990 capacitor Substances 0.000 title abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 14
- 229910052746 lanthanum Inorganic materials 0.000 claims description 5
- 229910052712 strontium Inorganic materials 0.000 claims description 5
- 229910052715 tantalum Inorganic materials 0.000 claims description 5
- 229910052719 titanium Inorganic materials 0.000 claims description 5
- 229910052779 Neodymium Inorganic materials 0.000 claims description 4
- 229910052788 barium Inorganic materials 0.000 claims description 4
- 229910052684 Cerium Inorganic materials 0.000 claims description 3
- 229910052777 Praseodymium Inorganic materials 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 229910052758 niobium Inorganic materials 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 239000010408 film Substances 0.000 description 47
- 150000002500 ions Chemical class 0.000 description 26
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- 238000010586 diagram Methods 0.000 description 7
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
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- 229910010413 TiO 2 Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
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- 229910021193 La 2 O 3 Inorganic materials 0.000 description 1
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- 229910052802 copper Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
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- 229910052737 gold Inorganic materials 0.000 description 1
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- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
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- 238000003980 solgel method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
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Definitions
- the present invention relates to a polycrystalline dielectric thin film and a capacitive element.
- a thin film using a metal oxide material has been widely used as the dielectric thin film.
- the improvement of the characteristics of the dielectric thin film by the metal oxide material is reaching its limit, and a new material having higher characteristics is demanded.
- One candidate for a new material is a metal oxynitride material in which a part of oxygen atoms in an oxygen octahedron having a perovskite crystal structure is replaced with a nitrogen atom.
- Patent Document 1 and Patent Document 2 describe a method for producing a powder of perovskite oxynitride ABO 2 N.
- Patent Document 1 and Patent Document 2 do not disclose anything about obtaining a thin film using perovskite oxynitride ABO 2 N.
- Non-Patent Document 1 and Non-Patent Document 2 describe that a thin film made of perovskite oxynitride ABO 2 N was produced.
- the thin film obtained in Non-Patent Document 1 and Non-Patent Document 2 is an epitaxial film.
- An epitaxial film is a thin film produced by epitaxial growth.
- Epitaxial growth is one of thin-film crystal growth techniques, and refers to crystal growth in which crystal growth is performed on a crystal serving as a substrate and aligned with the crystal plane of the underlying substrate.
- Non-Patent Document 1 describes that it takes a long time of 530 hours or less to produce an epitaxial film having a thickness of 20 nm or less.
- the present invention has been made in view of such a situation, and an object thereof is to provide a polycrystalline dielectric thin film and a capacitive element with high manufacturing efficiency and low dielectric loss.
- the polycrystalline dielectric thin film according to the present invention is a polycrystalline dielectric thin film whose main composition is a perovskite oxynitride,
- the polycrystalline dielectric thin film according to the present invention has the above characteristics, so that the dielectric loss can be reduced.
- the A is one or more elements selected from Sr, Ba, Ca, La, Ce, Pr, Nd, and Na.
- the B is preferably one or more elements selected from Ta, Nb, Ti and W.
- the polycrystalline dielectric thin film according to the present invention has an octahedral structure of BO 4 N 2 , and the arrangement of N in the octahedral structure is preferably cis type.
- the capacitive element according to the present invention includes the polycrystalline dielectric thin film.
- FIG. 1 shows a schematic diagram of a thin film capacitor according to this embodiment.
- a thin film capacitor 1 shown in FIG. 1 is formed on a substrate 11 in the order of a lower electrode 12 and a polycrystalline dielectric thin film 13, and includes an upper electrode 14 on the surface of the polycrystalline dielectric thin film 13.
- the material of the substrate 11 is not particularly limited, but using a Si single crystal substrate as the substrate 11 is excellent in availability and cost. When flexibility is important, Ni foil can be used as a substrate.
- the material of the lower electrode 12 and the upper electrode 14 is not particularly limited, and may function as an electrode.
- Pt, Ag, Ni, etc. are mentioned.
- the thickness of the lower electrode 12 is preferably 0.01 to 10 ⁇ m.
- the thickness of the upper electrode 14 is preferably 0.01 to 10 ⁇ m.
- the polycrystalline dielectric thin film 13 is a polycrystalline dielectric thin film whose main composition is a perovskite oxynitride.
- A may be any A site ion of the perovskite oxynitride.
- B may be a B site ion of the perovskite oxynitride.
- A is preferably one or more elements selected from Sr, Ba, Ca, La, Ce, Pr, Nd, and Na. It is more preferable to use one or more elements selected from Sr, Ba, La, and Nd because a high capacity can be obtained, and it is most preferable to use Sr.
- B is preferably one or more elements selected from Ta, Nb, Ti, and W. It is more preferable to use one or more elements selected from Ta and Ti because a polycrystalline dielectric thin film 13 with few different phases can be obtained, and Ta is most preferable.
- a / b is more preferably a / b ⁇ 1.05.
- n is more preferably n ⁇ 0.8.
- the total of the average valence of A site ions and the average valence of B site ions is 6.7 to 7.3.
- the total average valence is preferably 7 valences.
- the average valence is a value obtained by averaging the valences of ions existing at the A site and the B site according to their abundance ratios.
- Sr and La are present at a ratio of 4: 1 at the A site and Ta and Ti are present at a ratio of 4: 1 at the B site.
- the valence of Sr ions is 2, and the valence of La ions is 3. Therefore, when the average valence is ⁇ , ⁇ is calculated by the following equation (1).
- the total average valence ( ⁇ + ⁇ ) is 7.
- the perovskite oxynitride is Sr a Ta b O o N n
- the case where the A site element and / or the B site element are different elements is also applicable.
- the polycrystalline dielectric thin film 13 preferably has an octahedral structure of BO 4 N 2 and the arrangement of N in the octahedral structure is mainly cis type.
- the structure in which N has a cis arrangement is a structure in which two Ns are adjacent to each other as shown in FIG. 2A.
- the structure in which N takes the trans arrangement is a structure in which two Ns are not adjacent to each other as shown in FIG. 2B.
- FIGS. 3A and 3B are diagrams showing a case where a plurality of octahedral structures are connected in a case where N takes a cis arrangement and a case where N takes a trans arrangement. From FIG. 3A, it can be seen that when N takes a cis configuration, the crystal extends zigzag as seen from the c-axis direction. On the other hand, FIG. 3B shows that when N takes the trans arrangement, the crystal extends in a straight line in the c-axis direction. In addition, the c-axis length is longer when N takes a trans arrangement than when N takes a cis arrangement.
- N is mainly in the cis configuration. Even if neutron diffraction is not performed, if ABO 2 N is a polycrystal, it is known that N takes a stable cis configuration.
- ABO 2 N having a trans arrangement as described in Non-Patent Document 1, a substrate stress is applied to the single crystal of ABO 2 N by, for example, epitaxial growth on the substrate. It is necessary to prepare a state.
- the trans configuration is usually not completely zero.
- the cis arrangement Even if the cis arrangement is stable, the arrangement of some Ns may be disturbed due to thermal motion or the like, and may take a trans arrangement. Even in such a case, since the cis arrangement is dominant as an overall number, in the neutron diffraction, the result of the cis arrangement is obtained from the site existence probability.
- the polycrystalline dielectric thin film according to the present embodiment is a different type of thin film from the epitaxial film.
- N takes a trans configuration.
- XRD data of an epitaxial film in which the perovskite oxynitride is SrTaO 2 N is created, and the polycrystalline film according to the present embodiment is formed. What is necessary is just to confirm that there is no common peak compared with the XRD data of a dielectric thin film.
- FIG. 4 shows XRD data of an epitaxial film in which the perovskite oxynitride is CaTaO 2 N. Similar to FIG. 4, XRD data of the epitaxial film of SrTaO 2 N may be prepared. The fact that the thin film is a polycrystalline film can be confirmed by the fact that there is a peak in XRD data and the crystal plane derived from the peak is not only a specific crystal plane.
- the polycrystalline dielectric thin film 13 is a kind of polycrystalline film and a kind of dielectric thin film.
- the thickness of the polycrystalline dielectric thin film 13 is not particularly limited, but is preferably 10 nm to 1 ⁇ m.
- the method of forming the thin film that will eventually become the polycrystalline dielectric thin film 13 For example, vacuum deposition, sputtering, PLD (pulse laser deposition), MO-CVD (metal organic chemical vapor deposition), MOD (organic metal decomposition), sol-gel method, CSD (chemical solution deposition) And the like.
- the raw materials used during film formation may contain minute impurities and subcomponents, but there is no particular problem as long as the amount does not significantly impair the performance of the thin film.
- the polycrystalline dielectric thin film 13 according to the present embodiment may also contain minute impurities and subcomponents to such an extent that the performance is not significantly impaired.
- the finally obtained thin film tends to be a polycrystalline film.
- the polycrystalline dielectric thin film 13 according to the present embodiment is formed by a method such as a PLD method, a sputtering method, or a CSD method
- N tends to have a cis arrangement.
- synthesis is also possible by the CVD method, since the number of component elements is large, the PLD method and the sputtering method have higher composition controllability.
- a film forming method by the PLD method will be described.
- a Si single crystal substrate is prepared as the substrate 11.
- SiO 2 , TiO x , and Pt are sequentially formed on the Si single crystal substrate to form the lower electrode 12 made of Pt.
- the method for forming the lower electrode 12 is not particularly limited. For example, sputtering method, CVD, etc. are mentioned.
- a metal oxide thin film was formed on the lower electrode 12 by the PLD method. Further, in order to expose a part of the lower electrode 12, a metal mask was used to form a region where no thin film was formed.
- a target including a constituent element of a target polycrystalline dielectric thin film is placed in a film forming chamber.
- a pulse laser is irradiated on the surface of the target.
- the target energy is instantly evaporated by the strong energy of the pulse laser.
- an evaporant is deposited on the substrate arranged to face the target to form a metal oxide thin film.
- the type of target is not particularly limited, and in addition to a metal oxide sintered body containing constituent elements of a polycrystalline dielectric thin film to be produced, an alloy, a nitride sintered body, a metal oxynitride sintered body, or the like can be used. it can. Further, although it is preferable that each element is distributed on the average in the target, the distribution may vary within a range that does not affect the quality of the obtained polycrystalline dielectric thin film. Furthermore, the number of targets is not necessarily one, and a plurality of targets including a part of the constituent elements of the polycrystalline dielectric thin film can be prepared and used for film formation.
- the shape of the target is not limited and may be a shape suitable for the film forming apparatus to be used.
- the film forming conditions oxygen gas pressure, nitrogen gas pressure, film forming chamber size, gas introduction tube position, etc.
- the a / b of the polycrystalline dielectric thin film finally obtained is adjusted. Can be controlled. For example, if a / b of the target is increased, a / b in the formed film can be increased. Further, not only the target a / b but also the film forming conditions are important. This is because the metal element evaporated from the target by the pulse laser is affected by the elements constituting the atmosphere in the film formation chamber and reaches the film formation surface of the substrate.
- the composition of the finally obtained polycrystalline dielectric thin film is Sr a Ta b O o N n
- a sintered body containing Sr 2 Ta 2 O 7 is prepared as a target. Then, by adjusting the film forming conditions (for example, the gas pressure of oxygen, the gas pressure of nitrogen, the size of the film forming chamber, the position of the gas introduction pipe, etc.), the a / b can be controlled.
- the substrate 11 it is preferable to heat the substrate 11 with an infrared laser during film formation in order to crystallize the metal oxide thin film to be formed.
- the heating temperature of the substrate 11 varies depending on the constituent elements and composition of the metal oxide thin film and the substrate 11, for example, the film is formed by heating to 600 to 800 ° C.
- the temperature of the substrate 11 By setting the temperature of the substrate 11 to an appropriate temperature, the metal oxynitride thin film can be easily crystallized and the occurrence of cracks that occur during cooling can be prevented.
- the polycrystalline dielectric thin film 13 made of perovskite oxynitride can be obtained by introducing nitrogen radicals and performing nitriding during film formation.
- the thin film capacitor 1 can be manufactured by forming the upper electrode 14 on the polycrystalline dielectric thin film 13.
- the material of the upper electrode 14, Ag, Au, Cu etc. can be used.
- FIG. For example, it can be formed by a sputtering method.
- the capacitive element according to the present invention is an element using dielectricity, and includes a capacitor, thermistor, filter, diplexer, resonator, oscillator, antenna, piezoelectric element, transistor, ferroelectric memory, and the like.
- the polycrystalline dielectric thin film according to this embodiment is suitably used for a capacitor element that is particularly required to have a small dielectric loss.
- the SrCO 3 powder and Ta 2 O 5 powder were mixed for 16 hours by a wet ball mill using an ethanol solvent to obtain a mixed slurry.
- the mixed slurry was dried at 80 ° C. for 12 hours with a constant temperature dryer to obtain a mixture.
- the mixture was lightly crushed in a mortar and placed in a ceramic crucible. And it heat-processed for 2 hours at 1000 degreeC in air
- the calcined product was mixed again in a wet ball mill using an ethanol solvent for 16 hours to obtain a slurry after calcining.
- the obtained calcined slurry was dried at 80 ° C. for 12 hours with a constant temperature dryer to obtain a calcined mixture.
- a polyvinyl alcohol solution was added as a binder to the post-calcined mixture and mixed to obtain a granulated product.
- the addition amount of the polyvinyl alcohol solution was 0.6% by weight with respect to 100% by weight of the pulverized product.
- the granulated product was molded into a cylindrical shape having a diameter of about 23 mm and a height of about 9 mm to obtain a molded product.
- the molding method was CIP molding.
- the sintered product was fired at 1400 ° C. for 2 hours in an air atmosphere using an electric furnace to obtain a sintered product. Further, the upper and lower surfaces of the sintered product were mirror-polished to obtain a film formation target having a height of 5 mm. It was confirmed that the relative density of the obtained deposition target was 96 to 98%.
- the film formation target obtained as described above was placed in a film formation apparatus, and a Si substrate was placed so as to face the film formation target.
- a Si substrate a substrate having a Pt film as a lower electrode on the surface was used.
- a film was formed by a PLD method so as to have a thickness of 200 nm.
- the a / b of the finally obtained polycrystalline dielectric thin film was controlled by adjusting the film forming conditions (oxygen gas pressure, nitrogen gas pressure, etc.).
- a polycrystalline dielectric thin film was obtained by introducing nitrogen radicals and performing nitriding during film formation. The time required for film formation was 0.5 to 2 hours.
- the XRD pattern of the thin film sample obtained in Experimental Example 1 was measured using a fully automatic horizontal multipurpose X-ray diffractometer SmartLab manufactured by Rigaku Corporation. It was confirmed that all examples of Experimental Example 1 were not epitaxial films. Further, o and n in the obtained thin film sample were quantified by an impulse heating melt extraction method (infrared absorption method) using TC600 manufactured by LECO. Further, the valences of Sr ions and Ta ions were determined from XPS chemical shifts, and it was confirmed that there was no change in valence from the raw materials. Specifically, the valence of Sr ions was 2, and the valence of Ta ions was 5. Moreover, the value of a / b and the value of n were computed from the value quantified by the impulse heating melt extraction method.
- Dielectric loss was measured with an impedance analyzer (manufactured by Agilent Technologies) 4294A at a measurement voltage of 100 mV and a measurement frequency of 1 MHz.
- an impedance analyzer manufactured by Agilent Technologies 4294A at a measurement voltage of 100 mV and a measurement frequency of 1 MHz.
- the case where tan ⁇ was 10% or less was considered good.
- the results are shown in Table 1.
- Example 1 the dielectric loss of Example 1 in which a / b is greater than 1 was 1% or less. On the other hand, in Comparative Examples 1 and 2 in which a / b is 1 or less, the dielectric loss exceeded 1%.
- Example 11 and Comparative Example 11 Thin film samples of Example 11 and Comparative Example 11 were prepared in the same manner as in Experimental Example 1 except that La 2 O 3 powder and TiO 2 powder were used instead of SrCO 3 powder and Ta 2 O 5 powder, and various measurements were performed. Went. Furthermore, the thin film samples of Example 12 and Comparative Example 12 were produced in the same manner as in Experimental Example 1 except that BaO powder and Ta 2 O 5 were used, and various measurements were performed. Further, thin film samples of Example 13 and Comparative Example 13 were prepared in the same manner as in Experimental Example 1 except that Nd 2 O 3 powder and TiO 2 powder were used, and various measurements were performed. The results are shown in Table 2. In addition, the XRD measurement was performed about the thin film sample of the Example obtained in Experimental Example 2.
- Example 11 and Comparative Example 11 the valences of La ions and Ti ions were determined from the XPS chemical shift, and it was confirmed that there was no change in valence from the raw materials. Specifically, the valence of La ions was 3, and the valence of Ti ions was 4.
- Example 12 and Comparative Example 12 the valences of Ba ions and Ta ions were determined from XPS chemical shifts, and it was confirmed that there was no change in valence from the raw materials.
- the valence of Ba ions was 2, and the valence of Ta ions was 5. Furthermore, regarding Example 13 and Comparative Example 13, the valences of Nd ions and Ti ions were determined from XPS chemical shifts, and it was confirmed that there was no change in valence from the raw materials. Specifically, the valence of Nd ions was 3, and the valence of Ti ions was 4.
- Example 11 the dielectric loss of Example 11 in which a / b was greater than 1 was 1% or less. On the other hand, in Comparative Example 11 in which a / b was 1 or less, the dielectric loss exceeded 1%.
- Example 21 was obtained by changing the value of n.
- the results are shown in Table 3.
- n ⁇ 0.7 the structure in which the Ta—N chain is connected in a zigzag pattern is not sufficiently formed, and it is estimated that tan ⁇ deteriorates.
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Abstract
Description
前記ペロブスカイト型酸窒化物が組成式AaBbOoNn(a+b+o+n=5)で表され、
a/b>1
n≧0.7
であることを特徴とする。
前記BがTa,Nb,Ti,Wから選ばれる1種類以上の元素であることが好ましい。
=2×4/5+3×1/5
=2.2 ・・・式(1)
=5×4/5+4×1/5
=4.8 ・・・式(2)
次に、薄膜キャパシタ1の製造方法について説明する。以下、Aサイト原子をSr、Bサイト原子をTaとする場合について説明するが、他の種類の原子を用いる場合でも同様である。
まず、成膜用ターゲットとして用いるSr2Ta2O7焼結体の原料として、SrCO3粉末およびTa2O5粉末を準備した。Sr/Taのモル比が1となるようにSrCO3粉末およびTa2O5粉末を秤量した。
SrCO3粉末およびTa2O5粉末の代わりにLa2O3粉末およびTiO2粉末を用いた点以外は実験例1と同様にして実施例11および比較例11の薄膜サンプルを作製し、各種測定を行った。さらに、BaO粉末およびTa2O5を用いた点以外は実験例1と同様にして実施例12および比較例12の薄膜サンプルを作製し、各種測定を行った。さらに、Nd2O3粉末およびTiO2粉末を用いた点以外は実験例1と同様にして実施例13および比較例13の薄膜サンプルを作製し、各種測定を行った。結果を表2に示す。なお、実験例2で得られた実施例の薄膜サンプルについてXRD測定を行った。XRD測定により、実験例2の実施例および比較例も全てエピタキシャル膜ではなく多結晶薄膜であることを確認した。さらに、Nの配置がcis型であることを確認した。また、実施例11および比較例11に関して、LaイオンおよびTiイオンの価数をXPSのケミカルシフトから判定し、原料から価数の変化がないことを確認した。具体的には、Laイオンの価数は3で、Tiイオンの価数は4であった。実施例12および比較例12に関して、BaイオンおよびTaイオンの価数をXPSのケミカルシフトから判定し、原料から価数の変化がないことを確認した。具体的には、Baイオンの価数は2で、Taイオンの価数は5であった。さらに、実施例13および比較例13に関して、NdイオンおよびTiイオンの価数をXPSのケミカルシフトから判定し、原料から価数の変化がないことを確認した。具体的には、Ndイオンの価数は3で、Tiイオンの価数は4であった。
実施例1(n=0.8)について、nの値を変化させて実施例21および比較例21,22を得た。結果を表3に示す。
11・・・基板
12・・・下部電極
13・・・多結晶誘電体薄膜
14・・・上部電極
Claims (4)
- 主組成がペロブスカイト型酸窒化物である多結晶誘電体薄膜であって、
前記ペロブスカイト型酸窒化物が組成式AaBbOoNn(a+b+o+n=5)で表され、
a/b>1
n≧0.7
であることを特徴とする多結晶誘電体薄膜。 - 前記AがSr,Ba,Ca,La,Ce,Pr,Nd,Naから選ばれる1種類以上の元素であり、
前記BがTa,Nb,Ti,Wから選ばれる1種類以上の元素である請求項1に記載の多結晶誘電体薄膜。 - BO4N2の8面体構造を有し、前記8面体構造中におけるNの配置がcis型である請求項1または2に記載の多結晶誘電体薄膜。
- 請求項1~3のいずれかに記載の多結晶誘電体薄膜を有する容量素子。
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CN201780006873.5A CN108475580B (zh) | 2016-02-01 | 2017-02-01 | 多晶介电体薄膜及电容元件 |
KR1020187019705A KR20180094020A (ko) | 2016-02-01 | 2017-02-01 | 다결정 유전체 박막 및 용량 소자 |
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WO2020045446A1 (ja) * | 2018-08-31 | 2020-03-05 | Tdk株式会社 | 薄膜キャパシタおよび電子回路基板 |
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US11078123B2 (en) * | 2017-11-10 | 2021-08-03 | Tdk Corporation | Metal oxynitride thin film, process for producing metal oxynitride thin film, and capacitor element |
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WO2020045447A1 (ja) * | 2018-08-31 | 2020-03-05 | Tdk株式会社 | 誘電体薄膜、容量素子および電子回路基板 |
WO2020045446A1 (ja) * | 2018-08-31 | 2020-03-05 | Tdk株式会社 | 薄膜キャパシタおよび電子回路基板 |
JPWO2020045447A1 (ja) * | 2018-08-31 | 2021-08-10 | Tdk株式会社 | 誘電体薄膜、容量素子および電子回路基板 |
JPWO2020045446A1 (ja) * | 2018-08-31 | 2021-08-10 | Tdk株式会社 | 薄膜キャパシタおよび電子回路基板 |
US11532435B2 (en) | 2018-08-31 | 2022-12-20 | Tdk Corporation | Thin film capacitor and electronic circuit board |
JP7351304B2 (ja) | 2018-08-31 | 2023-09-27 | Tdk株式会社 | 誘電体薄膜、容量素子および電子回路基板 |
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