Single-crystal – oriented-crystal – and epitaxy growth processes; – Processes of growth from liquid or supercritical state – Having pulling during growth
Reexamination Certificate
2001-05-30
2003-01-14
Hiteshew, Felisa (Department: 1765)
Single-crystal, oriented-crystal, and epitaxy growth processes;
Processes of growth from liquid or supercritical state
Having pulling during growth
C117S014000, C117S015000
Reexamination Certificate
active
06506250
ABSTRACT:
BACKGROUND OF THE INVENTION
The invention relates to a method of producing multi-crystalline semiconductor material by crystallisation from a melt of a base material. A preferred but not exclusive field of application of the invention relates to the production of multi-crystalline silicon for photovoltaic purposes. The expression “multi-crystalline” is generally intended in this case to refer to the fact that it also comprises structures having relatively small grain sizes which are otherwise frequently described as “polycrystalline”.
For the purpose of conserving energy in the future, energy sources are now being developed which convert solar rays into electrical energy by utilizing the photovoltaic effect. Low process costs in the processing of base materials to form semiconductor materials and high levels of photovoltaic efficiency have proven to be the key operating points for developing this technology further.
For photovoltaic applications, silicon is now preferably used which, as a starting material for solar cell production, can be divided into three groups: mono-crystalline generated crystals from Czochralski-installations; materials having a poly- or multi-crystalline structure from block crystallisation or foil drawing installations; thin layer material (generally consisting of Chemical Vapour Deposition). Owing to the comparatively lower process costs, the two first mentioned variations are frequently preferred, in which the crystallization is performed from a melt of a base material.
In the production of semiconductor materials by crystallization from a melt, phase-transition takes place together with cooling from high temperature ranges. Process conditions which can effect specific damage to the crystal structure are associated with these processes in dependence upon the process control and solidification rates and cooling rates. However, each type of disruption to an ideal crystal structure leads to a more or less considerable reduction in the electrical efficiency of the components, such as solar cells, which are manufactured from these materials.
It has been discovered that amongst the various crystal defects it is principally the density of crystal dislocations which contributes very substantially to the deterioration in electrical efficiency of semiconductor elements, in particular for limiting the efficiency of solar cells. Mono-crystalline drawn silicon, such as e.g. from Czochralski-installations, generally does not contain any dislocations of this kind; however, owing to the still relatively high production costs it is too expensive for the mass-production of solar cells. Multi-crystalline silicon, which can be produced from the melt in a shorter period of time, is a much more cost-effective option and is thus more readily available for the purpose of an extensive application. On the other hand, this material contains the said crystal dislocations, and the less favourable the cooling time during crystallisation, the greater the dislocation density.
Normally, after both phase-transition from the melt to the solid body and also during the subsequent cooling to room temperature, thermally induced stresses are produced in the material which in turn lead to a plastic deformation by the formation of crystal dislocations. The dislocations are extremely mobile close to the melting point, which is to be equated with a high degree of plasticity in the material. During further cooling, the rate at which these dislocations pass through the crystal decreases and specific dislocation structures are formed in dependence upon the process control. It is desired to reduce the dislocations but this could hitherto only be achieved by reducing the cooling rate, i.e. by prolonging the process time. This increases considerably the cost of the production process because the operational time of the production installation is a significant-cost factor.
Tests have shown that the crystal dislocations can be reduced significantly by virtue of mechanical action upon the melt during the phase-transition and/or also during the subsequent cooling to room temperature. More precisely, it has been found that the aforementioned conversion process from thermally induced macroscopic stresses to universal dislocation arrangements or dislocation arrangements which are distributed locally in the material volume can be influenced by coupling vibration energy in the sonic or ultrasonic range such that the total number of dislocations is reduced and in contrast other stress-relaxing mechanisms are favoured such as e.g. twin-formation. Experiments have demonstrated that these crystal twins contribute considerably less than dislocations to the reduction in electrical efficiency in particular in the case of solar cells.
SUMMARY OF THE INVENTION
In the case of the present invention, this knowledge is utilized for the purpose of achieving the object of obtaining a multi-crystalline semiconductor material by crystallization from a melt in such a manner that the ratio between process duration and dislocation density is more favourable than before. In order to achieve this, in accordance with the invention vibration energy is coupled in the sonic or ultrasonic range into the solidifying or cooling material during solidification of the melt and/or during the subsequent further cooling, wherein these parameters of this vibration energy coupling are harmonised with the parameters of the melt and the cooling time such that the dislocation density in the cooled multi-crystalline material is considerably lower than in the case where there is no vibration energy coupling during the respective cooling time. The term “cooling time” in this context is intended to refer to the total period of time from the commencement of the liquid/solid phase-transition up to complete cooling to room temperature.
Therefore, the invention achieves a considerable improvement in the hitherto conventional methods, in that it is possible either to reduce the dislocation density for a given process time or to shorten the process time with the dislocation density remaining unchanged or to achieve a more effective compromise between these two parameters than previously was the case.
Preferably, the frequency, intensity and the type of coupling of vibration energy are optimized in such a manner that the desired effect of a reduced dislocation density or a preferable formation of twins is achieved in the most effective manner possible. Alternatively, the method in accordance with the invention can also be applied in order to shorten the cooling time and thus the process time whilst accepting a less considerable reduction in the dislocation density, thus rendering the method more cost-effective.
The invention can be applied in the case of block crystallization methods and foil drawing methods. The vibration energy can be coupled-in via solid-borne sound or acoustically via a gaseous transmission medium such as e.g. air or a protective gas. In the latter case in particular, it is possible in one particular embodiment of the invention to perform the coupling-in process in a resonator-like manner, in that a standing acoustic wave is generated between a surface of the solidifying or cooling material and an acoustic reflector.
Tests to improve the electronic properties of silicon material by means of ultrasonic treatment are known per se (Appl. Phys. Lett. 68: 2873-2875). The influence of defects in crystalline semiconductor structures by means of ultrasound is also reported on in the Abstracts I10 and O43 in two contributions by S. Ostapenko and by I. V Ostrovskii inter alia at the conference “Polyse ‘98” (Schwäbisch Gmünd, 13.-18.9.1998). However, these tests were only carried out after actual crystal generation and at low temperatures up to 150° C. They also did not influence the crystal defects such as dislocations, but exclusively influenced the occurrence of point defects in the treated samples.
The process of influencing the production of crystalline semiconductor structures in situ by means of ultrasound is likewise known per se, and furt
Breitenstein Otwin
Franke Dieter
Dennison, Schultz & Dougherty
Hiteshew Felisa
Max-Planck -Gesellschaft zur Forderung der Wissenschaften e.V.
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