This application is based upon and claims the benefit of priority of the prior Japanese Patent Application No. 2015-202307, filed on Oct. 13, 2015, the entire contents of which are incorporated herein by reference.
The embodiments discussed herein are related to a thermoelectric conversion element, a method for producing the thermoelectric conversion element, and the like.
Attention has been focused on thermoelectric conversion elements, which are clean power generation systems, from the viewpoint of a reduction in carbon dioxide (CO2) emission and environmental protection. Use of thermoelectric conversion elements enables thermal energy, which has previously been exhausted, to be converted into electric energy and reused.
There may be room for increasing the thermoelectric efficiency of thermoelectric conversion elements.
Japanese Laid-open Patent Publication Nos. 2006-179807 and 2006-24632 disclose the related art.
Accordingly, it is desired to provide a thermoelectric conversion element, a method for producing the thermoelectric conversion element, and the like that have an increased thermoelectric efficiency.
According to an aspect of the invention, a thermoelectric conversion element includes a p-type film having a perovskite structure, the p-type film including Co; an n-type film having a perovskite structure, the n-type film including Ti; first and second i-type films configured to be arranged to face each other across the n-type film, the first and second i-type films having a perovskite structure and including Ti; and a barrier film configured to be interposed between a multilayer body and the p-type film, the barrier film having a perovskite structure and including Zr, the multilayer body including the n-type film and the first and second i-type films.
According to another aspect of the invention, a method for producing a thermoelectric conversion element, the method includes: forming a p-type film having a perovskite structure, the p-type film including Co; forming an n-type film having a perovskite structure, the n-type film including Ti; forming first and second i-type films having a perovskite structure, the first and second i-type films including Ti and being arranged to face each other across the n-type film; and forming a barrier film configured to be interposed between a multilayer body and the p-type film, the barrier film having a perovskite structure and including Zr, the multilayer body including the n-type film and the first and second i-type films.
The object and advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the claims.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory and are not restrictive of the invention, as claimed.
The embodiments are specifically described below with reference to the attached drawings.
The first embodiment is described below. There is described an example of a thermoelectric conversion element as the first embodiment.
A thermoelectric conversion element 10 according to the first embodiment includes a p-type film 1, an n-type film 2, and i-type films 3 and 4. The i-type films 3 and 4 are arranged to face each other across the n-type film 2 as illustrated in
The p-type film 1 has a perovskite structure and includes Co. The thickness of the p-type film 1 is preferably 100 to 10,000 nm in order to achieve a sufficient amount of current. The n-type film 2 and the i-type films 3 and 4 have a perovskite structure and include Ti. The thickness of the n-type film 2 is preferably 10 nm or more in order to achieve a sufficient amount of current. The thickness of the n-type film 2 is preferably 100 nm or less in order to reduce the influence of electrons migrating from the n-type film 2 into the i-type films 3 and 4. The thicknesses of the i-type films 3 and 4 are preferably 1 to 5 nm in order to reduce the influence of electrons migrating from the n-type film 2 into the i-type films 3 and 4. The barrier films 5 and 6 have a perovskite structure and include Zr. The thicknesses of the barrier films 5 and 6 are preferably 5 nm or more in order to achieve an appropriate degree of insulating capability. However, the insulating capability of the barrier films 5 and 6 stops increasing when the thicknesses of the barrier films 5 and 6 reach about 100 nm, and setting the thicknesses of the barrier films 5 and 6 to be more than 100 nm only increases the cost. Thus, the thicknesses of the barrier films 5 and 6 are preferably 100 nm or less. The p-type film 1 is a p-type LaCoO3 film or the like. The n-type film 2 is an n-type Sr0.95La0.05TiO3 film or the like. The i-type films 3 and 4 are, for example, SrTiO3 films that are not intentionally doped with impurities. The barrier films 5 and 6 are SrZrO3 films or the like.
The p-type film 1 is interposed between the barrier films 5 and 6. There is a difference (ΔVB) in the energy of the valence band between LaCoO3 and SrZrO3 as illustrated in
In the thermoelectric conversion element 10, for example, the p-type film 1 and the n-type film 2 are electrically coupled to each other with a conductive film 7, and a conductive film 8 is arranged to come into contact with the p-type film 1 and the n-type film 2 on a side of the thermoelectric conversion element 10 which is opposite to the side on which the conductive film 7 is present. In this case, the difference in temperature between the vicinity of the conductive film 7 and the vicinity of the conductive film 8 creates a voltage, which is output from the conductive film 8. Since the difference (ΔVB) in the energy of the valence band is 3.5 eV in the first embodiment, the p-type film 1 serves as a p-type quantum well. This enables quantum confinement to be achieved and may increase a figure of merit (ZT), which is a measure of thermoelectric efficiency.
The thermoelectric conversion element 10 may be produced by, for example, forming the barrier film 6, the p-type film 1, the barrier film 5, the i-type film 3, the n-type film 2, the i-type film 4, and the barrier film 6 on and above a substrate in this order. The above films may be formed in inverse order. The substrate may be (LaAlO3)0.3—(SrAl0.5Ta0.5O3)0.7, which is a LSAT substrate, or the like. For forming the barrier film 6, the p-type film 1, the barrier film 5, the i-type film 3, the n-type film 2, the i-type film 4, and the barrier film 6, for example, pulsed laser deposition (PLD) may be employed. In PLD process, for example, a Q-switched Nd:YAG laser is used, the pulse rate is set to 10 Hz, and the interval between the substrate and a target is set to 5 cm. For forming the barrier film 6, the p-type film 1, the barrier film 5, the i-type film 3, the n-type film 2, the i-type film 4, and the barrier film 6, alternatively, RF magnetron sputtering may be employed.
The second embodiment is described below. In the second embodiment, an example of a thermoelectric conversion apparatus is described.
A thermoelectric conversion apparatus 20 according to the second embodiment includes three thermoelectric conversion elements 10 that are stacked on top of one another as illustrated in
In the thermoelectric conversion apparatus 20, the difference in temperature between the heat sinks 12 and 14 creates a voltage, which is output from the conductive films 8 disposed at the respective ends of the thermoelectric conversion apparatus 20. Since the difference (ΔVB) in the energy of the valence band is 3.5 eV in the second embodiment, the p-type films 1 serve as p-type quantum wells. This may increase the thermoelectric efficiency of the thermoelectric conversion apparatus.
A test conducted by the inventors of the present application is described below. In this test, a LaCoO3 film was formed on a SrTiO3 substrate doped with Nb (1 mass %) by PLD. For performing ablation, a Q-switched Nd:YAG laser was used, the pulse rate was set to 10 Hz, and the interval between the substrate and a target was set to 5 cm. The target used was a polycrystalline LaCoO3 target having a stoichiometric composition. While the LaCoO3 film was formed, X-ray photoelectron spectroscopy (XPS) analysis was conducted on site.
As illustrated in
As illustrated in
The results of the above analysis and ultraviolet photoelectron spectroscopy (UPS) analysis confirm that the difference in the energy of the valence band between SrTiO3 and LaCoO3 was 3.0 eV.
The p-type film 1 is not limited to a LaCoO3 film and may be, for example, a SraLa1-aCoO3 film (0≤a≤0.5) or a CabLa1-bCoO3 film (0≤b≤0.5). The n-type film 2 is not limited to a Sr0.95La0.05TiO3 film and may be, for example, a Sr1-cLacTiO3 film (0.01≤c≤5) or a SrTi1-dNbdO3 film (0.01≤d≤0.5). The barrier film 5 is not limited to a SrZrO3 film and may be a SrZr1-eTieO3 film (0≤e≤0.8). The p-type film 1 may be constituted by a plurality of sublayers.
All examples and conditional language recited herein are intended for pedagogical purposes to aid the reader in understanding the invention and the concepts contributed by the inventor to furthering the art, and are to be construed as being without limitation to such specifically recited examples and conditions, nor does the organization of such examples in the specification relate to a showing of the superiority and inferiority of the invention. Although the embodiments of the present invention have been described in detail, it should be understood that the various changes, substitutions, and alterations could be made hereto without departing from the spirit and scope of the invention.
Number | Date | Country | Kind |
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2015-202307 | Oct 2015 | JP | national |
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4938244 | Kumada | Jul 1990 | A |
20080295879 | Atanackovic | Dec 2008 | A1 |
20090107535 | Hu | Apr 2009 | A1 |
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Number | Date | Country |
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2006-024632 | Jan 2006 | JP |
2006-179807 | Jul 2006 | JP |
WO 2013171834 | Nov 2013 | WO |
Number | Date | Country | |
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20170104145 A1 | Apr 2017 | US |