Process for producing thermoelectric material

Batteries: thermoelectric and photoelectric – Thermoelectric – Processes

Reexamination Certificate

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Details

C136S238000, C136S240000, C419S033000, C419S038000, C419S048000, C419S056000

Reexamination Certificate

active

06403875

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a process for producing a thermoelectric material which can be used as a material of thermoelectric devices utilizing Peltier effect or Seebeck effect. More particularly, it relates to a process of producing a thermoelectric material, in which grinding and normal sintering or hot pressing are carried out in the presence of a specific solvent to bring about a markedly improved figure of merit.
2. Description of Related Art
Thermoelectric devices utilizing Peltier effect have found wide application as thermoelectric electricity generators, thermosensors, etc.
Performance properties of thermoelectric materials which can provide thermoelectric devices are evaluated by the thermoelectric figure of merit Z which is obtained from Seebeck coefficient &agr;, thermal conductivity &kgr;, and electrical resistivity &rgr; (or electrical conductivity &sgr;) as represented by equation:
Z=&agr;
2
/(&rgr;·&kgr;)=&agr;
2
·&sgr;/&kgr;
That is, in order to improve the figure of merit (to increase the figure of merit) of a thermoelectric material, it is required that the Seebeck coefficient be high, and both the specific resistance and the thermal conductivity be low.
The following process is adopted to produce a thermoelectric material for obtaining a p-type or n-type thermoelectric device, the material comprising an appropriately doped alloy comprising at least two elements selected from the group consisting of Bi, Te, Se and Sb elements. The process comprises mixing weighed amounts of Bi, Te, Se or Sb powder and a dopant, melting the mixture, grinding the resulting alloy ingot to powder, and sintering the powder to obtain a thermoelectric material as a sintered body.
Sintering techniques used here include normal sintering, hot pressing, vacuum sintering, gas-pressure sintering, plasma sintering, and hot isostatic press sintering (HIP). Normal sintering and hot pressing are particularly preferred. Normal sintering is practical for ease in producing a sintered body of complicated configuration and also from the economical standpoint. Hot pressing provides a sintered body with few cracks and excellent mechanical strength.
However, the figure of merit Z of thermoelectric materials obtained by normal sintering, hot pressing, etc. is lower than the desired range. It has been a demand to produce a thermoelectric material having a high figure of merit Z. In particular, considered that the figure of merit Z of available p-type thermoelectric devices exceeds 3.0×10
−3
K
−1
, whereas those of available n-type ones are around 2.5×10
−3
K
−1
, there has been a keen demand to further improve the figure of merit of n-type thermoelectric devices.
SUMMARY OF THE INVENTION
An object of the present invention is to provide an economically excellent process for producing a thermoelectric device having a low carrier density, a high mobility, and a greatly improved figure of merit.
As a result of investigation, the present inventors have found that the above object is accomplished by the presence of a specific solvent in grinding an alloy ingot obtained by mixing and melting and also in normal sintering or hot pressing the resulting powder.
The present invention has been completed based on the above finding. The present invention provides a process for producing a thermoelectric material comprising mixing at least two members selected from bismuth, tellurium, selenium, and antimony and, if desired, a dopant, melting the mixture, grinding the resulting alloy ingot, forming the powder, and sintering the green body under normal pressure, which is characterized in that the grinding and the normal sintering are carried out in the presence of a solvent represented by formula: C
n
H
2n+1
OH or C
n
H
2n+2
CO (wherein n is 1, 2 or 3).
The present invention also provides a process for producing a thermoelectric material comprising mixing at least two members selected from bismuth, tellurium, selenium, and antimony and, if desired, a dopant, melting the mixture, grinding the resulting alloy ingot, and hot pressing the powder, which is characterized in that the grinding and the hot pressing, are carried out in the presence of a solvent represented by formula: C
n
H
2n+1
OH or C
n
H
2n+2
CO (wherein n is 1, 2 or 3).
The thermoelectric material obtained by the process of the invention has a low carrier density, a high mobility, and a satisfactory figure of merit. Where normal sintering is adopted, the process is economically excellent. The thermoelectric material thus obtained are applicable to various fields as a thermoelectric device with its Peltier effect being taken into advantage of.
DETAILED DESCRIPTION OF THE INVENTION
The process for production according to the present invention will hereinafter be described in detail.
At least two members selected from bismuth, tellurium, selenium and antimony are used in the present invention as constituent elements of the thermoelectric material.
A dopant is used in addition if necessary to obtain a desired n-type thermoelectric device or a desired p-type thermoelectric device. Such a dopant includes BiF
3
, BiCl
3
, BiBr
3
, BiI
3
, TeCl
4
, TeI
2
, TeI
4
, TeBr
4
, SeCl
4
, SeBr
4
, SeI
4
, SbF
3
, SbCl
3
, SbCl
5
, SbBr
3
, Se, and Te.
Weighed amounts of the constituent elements and the dopant for a thermoelectric material are mixed and melted. After mixing in a molten state, the melt is cooled to obtain an alloy ingot.
The resulting alloy ingot is round in a solvent represented by formula: C
n
H
2n+1
OH or C
n
H
2n+2
CO (wherein n is 1, 2 or 3) by means of a vibration mill, etc. to obtain an alloy powder having an average particle size of 0.5 to 50 &mgr;m.
The solvent represented by formula: C
n
H
2n+1
OH or C
n
H
2n+2
CO (wherein n is 1, 2 or 3) is methanol, ethanol, propanol, acetaldehyde, acetone or methyl ethyl ketone, with methanol or acetone being preferred. Use of such a solvent brings about an improvement on the figure of merit Z of the resulting thermoelectric material.
It is preferred for the solvent to have a dielectric constant of 21.4% or higher at 20° C., a dipole moment of 1.68×10
−16
c.s.u or higher, a molecular weight of 58.1 or lower, and a boiling point of 55 to 79° C.
Then the alloy powder is formed and sintered under normal pressure, or the alloy powder is hot pressed.
In the case of powder forming, followed by normal sintering, forming is preferably conducted by uniaxial pressing or cold isostatic pressing (CIP). Pressing provides a green body with an increased density.
The green body is subjected to normal sintering in the presence of the solvent at 300 to 600° C., desirably for 0.1 to 10 hours. Normal sintering in the presence of the solvent brings about improvement on the figure of merit Z of the thermoelectric material.
The normal sintering is preferably effected in two stages. Specifically, the green body of the alloy powder is heated in hydrogen gas and maintained at 300 to 600° C. for 1 to 60 minutes and then further heated in an inert gas, such as argon gas, and held at 400 to 600° C. for 1 to 60 minutes, followed by cooling.
In the case where the allow powder is hot pressed, hot pressing is performed in the presence of the solvent. Hot pressing is preferably conducted in a non-oxidizing gas atmosphere, e.g., an a room atmosphere, at 400 to 600° C. for 0.1 to 10 hours. Hot pressing in the presence of the solvent produces an improvement in the figure of merit Z of the thermoelectric material.
There is thus obtained a thermoelectric material comprising a sintered body. Specific examples of the thermoelectric material include bismuth telluride, bismuth selenide, antimony telluride, antimony selenide, bismuth sulfide, antimony sulfide, etc., which can be used either individually or as a combination thereof. Polycrystalline materials made up of a single compound such as bismuth telluride, bismuth selenide, etc. or a solid solution of these compounds are used as a mate

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