This application claims the priority benefit of Taiwan application serial no. 99106968, filed on Mar. 10, 2010. The entirety of the above-mentioned patent application is hereby incorporated by reference herein and made a part of this specification.
The disclosure relates to a method for producing a thermoelectric material, and more generally to a method for producing a thermoelectric material having a high thermoelectric figure of merit ZT.
Thermoelectric material is one of the simplest technologies for energy conversion. Through conduction electrons of thermoelectric material, heat energy transfer to electrical power or move from cold side to hot side in a non-mechanical manner. Therefore, thermoelectric material has the potential for applying in cogeneration, portable electric power and air-conditions system.
The energy conversion efficiency of a thermoelectric material is closely related to the dimensionless thermoelectric figure of merit ZT. The thermoelectric figure of merit ZT=S2σ/k, wherein S is a Seebeck coefficient, σ is an electrical conductivity, and k is a thermal conductivity. With increasing performance of the thermoelectric material, the efficiency of a thermoelectric cooler or a thermoelectric power generator will be increased. Conventional thermoelectric materials, have been developed from 1960's, is limited to ZT=1.0 at room temperature. Currently, many researches focus on the development of thermoelectric material with nanostructure and ZT got important breakthrough to 1.5 to 2.0.
A high performance thermoelectric material is with high Seebeck coefficient, high electrical conductivity and low thermal conductivity. Since an increase in Seebeck coefficient normally implies with a decrease in electrical conductivity. Increasing carrier concentration means an increment of electrical conductivity and implies the decreasing in Seebeck coefficient and increasing in thermal conductivity. Therefore, the material is intrinsically with the limitation of ZT value.
To enhance the thermoelectric figure of merit, the main research focuses on the development of nanostructurenanostructurenano composite thermoelectric material which having a small energy band gap. That is, the optimization between the Seebeck coefficient, thermal conductivity and electrical conductivity is obtained by changing the dopant, doping level and the nanostructure of the material, so as to achieve the maximum thermoelectric figure of merit value.
The disclosure provides a method for producing a thermoelectric material is with high dimensionless thermoelectric figure of merit.
The disclosure further provides a method for producing a thermoelectric material, and significantly enhances the electrical conductivity and decrease thermal conductivity in the same time.
The disclosure provides a method for producing a thermoelectric material. First, a semiconductor material powder is provided. Thereafter, an electroless plating processes deposit metal nano-particles on the surface of semiconductor material powder. Subsequently, an electrical current activated sintering process is performed to fabricate a thermoelectric material with one and plurality grain boundaries.
The disclosure further provides a method for producing a thermoelectric material. A sensitized semiconductor material powder mixed into a metal ion solution, wherein a part or all of metal ions attach on the surface of semiconductor powder. Afterwards, as reducing agent added into the mixture, the metal ions attached on the surface of semiconductor material powder are reduced to metal nano-particles deposit on the surface of semiconductor material powder. Furthermore, an electrical current activated sintering process is performed to form a thermoelectric material with one and plurality grain boundaries.
As mentioned above, in the process of producing the nanostructured thermoelectric material of the disclosure, the electroless plating process is performed to deposit nano-particles on the surface of a semiconductor material powder, and an electrical current activated sintering process is then performed, so that the produced thermoelectric material can has a better Seebeck coefficient, a higher electrical conductivity and a lower thermal conductivity, and thus has a higher thermoelectric figure of merit value.
Several exemplary embodiments accompanied with figures are described in detail below to further describe the disclosure in details.
The accompanying drawings are included to provide further understanding, and are incorporated in and constitute a part of this specification. The drawings illustrate exemplary embodiments and, together with the description, serve to explain the principles of the disclosure.
Thereafter, in the step 102, an electroless plating process is performed to deposit one and plurality metal nano-particles on the surface of semiconductor material powder. The material of the metal nano-particles can be silver (Ag), tin (Sn), copper (Cu) or palladium (Pd), for example. The material of the metal nano-particles can be selected depending on the conductivity type of the thermoelectric material to be formed. For example, when the required thermoelectric material is N-type, silver can be selected as the material of the metal nano-particles; when the required thermoelectric material is P-type, tin can be selected as the material of the metal nano-particles.
The silver nano-particles are taken as an example to illustrate the electroless plating process of the disclosure in the following. First, a sensitization is performed to the semiconductor material powder provided in the step 100. Thereafter, the semiconductor material powder is centrifugal extracted and then immersed into silver ammonia solution. The silver ions are attached on the surface of semiconductor material powders. The semiconductor material powders are centrifugal extracted. Next, the extracted semiconductor powders immerse into reducing agent and silver ions reduced to silver nano-particles deposit on the surface of semiconductor material powder. Last, centrifugal extraction and a water rinse are performed to get one and plurality dry semiconductor powder. It is noted that in this electroless plating process, the reducing agent is added after the silver ions are attached on the surface of semiconductor material powder. However, in another electroless plating process, as the semiconductor material powder immerse into the silver ammonia solution, the reducing agent add to this solution in the same time.
During the electroless plating process, a solution containing reducing ions with high adhesion to the surface of semiconductor material powder is selected as the reducing agent, so that the surface of the semiconductor material powder is functionalized to attract more metal nano-particles to deposit on the surface of the semiconductor material powder uniformly.
Afterwards, in the step 104, an electrical current activated sintering process is performed to the semiconductor material powder with the metal nano-particles deposited thereon, so as to form a thermoelectric material with one and plurality grain boundaries. The electrical current activated sintering process can be a spark plasma sintering (SPS) process, for example. After the electrical current activated sintering process, a part of the metal nano-particles are doped into the thermoelectric material for adjusting the conductivity type of the thermoelectric material, and further adjusting the thermoelectric property of the same. In addition, another part of the metal nano-particles are still present on the grain boundary to produce one and plurality nano-heterogeneous boundaries, as shown in
During the electrical current activated sintering process, a solid solution is formed by a part of the metal nano-particles and the semiconductor material powder, so as to increase the carrier concentration and the thermoelectric power factor. Further, the lower sintering temperature and the shorter sintering time, compared with conventional smelting process, reduced the atomic diffusion effect and effectively maintained the micro- or nano-structure inside the thermoelectric material. In addition, a part of the metal nano-particles are present on the grain boundary to produce one and plurality nano-heterogeneous boundaries, so as to cause an effect similar to the quantum effect, thereby enhancing the Seebeck coefficient. Moreover, during the electrical current activated sintering process, the metal nano-particles on the grain boundary can produce the scattering effect for phonons, and the metal nano-particles can restrain the grain growth of the semiconductor material while maintain the nano-grains of the same. Accordingly, the metal nano-particles can effectively reduce the thermal conductivity.
An electroless plating process is performed to deposit metal nano-particles on the surface of semiconductor material powders, and an electrical current activated sintering process is then performed to produce a thermoelectric material. In some exemplary embodiments, the metal nano-particles can be uniformly distributed on the surface of the semiconductor material powder, the thermoelectric power factor can be increased, the microcrystalline structure can be maintained in the material, the Seebeck coefficient can be increased and the thermal conductivity can be reduced.
An example and a comparative example are provided below to illustrate a method for producing a thermoelectric material of the disclosure.
First, PbTe powder was dipped in a solution formed by HCl and SnCl2, and the mixture was stirred with a magnetic stirring bar at room temperature for range 1 to 5 minutes, so that Sn2+ ions were adsorbed on the PbTe powder to complete the sensitization of the PbTe powder. Thereafter, the PbTe powder was centrifugal extracted. Afterwards, the extracted one and plurality PbTe powders immerse into silver ammonia solution formed by NaOH, NH4OH and AgNO3. Meanwhile, the Sn2+ ions on the PbTe powder made Ag+ ions attach on the surface of PbTe powder and centrigual extracted the PbTe powder. Further, the extracted one and plurality PbTe powders immerse into reducing agent containing C6H12O6, so that the Ag+ ions attached on the PbTe powder were reduced to Ag nano-particles deposit on the surface of PbTe powder. Next, a spark plasma sintering process was performed to the PbTe powder having the Ag nano-particles under high pressure range from 50 to 100 MPa at the temperature greater than 300° C. Thereafter, a cooling process was performed to obtain a thermoelectric material.
First, a high energy ball milling process was performed to grind a PbTe material into PbTe powder. Next, a spark plasma sintering process was performed to the PbTe powder under the pressure of 100 MPa at the temperature greater than 300° C. Thereafter, a cooling process was perform to obtain a thermoelectric material.
The thermoelectric material of the example (using an electroless plating process and an electrical current activated sintering process when produced) is compared with that of the comparative example (not using an electroless plating process when produced) in the following.
In summary, in the disclosure, an electroless plating process and a electrical current activated sintering process are sequentially performed to produce a thermoelectric material with nanostructure inside, so that the produced thermoelectric material has a better Seebeck coefficient, a higher electrical conductivity and a higher thermoelectric power factor. That is, the thermoelectric material fabricated by the method in accordance with the disclosure has a higher thermoelectric figure of merit value.
It will be apparent to those skilled in the art that various modifications and variations can be made to the structure of the disclosed embodiments without departing from the scope or spirit of the disclosure. In view of the foregoing, it is intended that the disclosure cover modifications and variations of this disclosure provided they fall within the scope of the following claims and their equivalents.
Number | Date | Country | Kind |
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99106968 A | Mar 2010 | TW | national |
Number | Name | Date | Kind |
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6793875 | Shaw et al. | Sep 2004 | B1 |
20010055685 | Kaneyoshi | Dec 2001 | A1 |
Number | Date | Country | |
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20110223350 A1 | Sep 2011 | US |