CZ Method
CZ Method
CZ Method
The apparatus used for CZ method of crystal growth is called puller having weight of 17,600 kg and is 6.5 m tall. The puller can hold a melt charge of 60 kg of Silicon, which can be transformed into a crystal of 100 mm diameter and 3.0 m length. The puller has 4 subsystems which are as follows: 1. Furnace: crucible, susceptor, rotation mechanism, heating element, power supply and chamber. 2. Crystal-pulling mechanism: seed shaft or chain, rotation mechanism and seed chuck. 3. Ambient control: gas source, flow control, purge tube and exhaust or vacuum system. 4. Control system: microprocessor, sensors and outputs. Furnace: It consist of crucible which contains the molten silicon, hence crucible material should be unreactive with molten silicon. This is a major consideration, because the electrical properties of silicon are sensitive to even ppb levels of impurities. Other characteristics of crucible material are a high melting point, thermal stability and hardness. The materials used
1|Prepared by Vimal Kant Pandey
Growth in a vacuum meets these requirements; it also has the advantage of removing SiO from the system thus preventing its buildup inside furnace chamber. Growth in gaseous atmosphere generally used for large growers, must use an inert gas such as He or Argon.
Fig: Temperature gradient, solidification and transport process in CZ method The heat transfer conditions about the interface can be modeled by the following equation:
-----------(1) Where L = latent heat of fusion; dm/dt = mass solidification rate; T= temperature; kl and ks are thermal conductivities of liquid and solid; dT/dx1 and dT/dx2 are thermal gradients at point 1 and 2; A1 and A2 are the area of isotherms at position 1 & 2. From equation 1 maximum pull rate of a crystal under condition of zero thermal gradient in the melt (i.e. dT/dx1=0 ) can be deduced. Converting the mass solidification rate to growth rate using density and area yields
The pull rate influence the incorporation of impurities into the crystal and is a factor in defect generation. Generally, when the temperature gradient in the melt is small, the heat transferred to the crystal is the latent heat of fusion. As a result, the pull rate varies inversely with diameter. The pull rate obtained in practice is 30% to 50% slower than the maximum values suggested by theoretical consideration. Growth rate or growth velocity of the crystal is actually distinct from the pull rate. Pull rate is the macroscopic indication of the net solidification rate, whereas growth rate is the instantaneous solidification rate. The two are differ because of temperature fluctuations at interface. The growth rate can exceed pull rate or even be negative at a given time. When it is negative remelting is said to be occur. The growth rate influences the defect structure and dopant distribution in the crystal on a microscopic scale. Pull rate affects the defects properties in the following way: the condensation of the thermal point defects into small dislocation loops occurs as the crystal cools from the solidification temperature. This process occurs above 9500C. The number of defects depends upon cooling rate, which is function of pull rate and diameter at 9500C. A pull rate of 2 mm/min eliminates defect formation from quenching the point defects. A related phenomenon remelting can also be suppressed by attaining a pull rate of 2.7 mm/min which is half of Vmax.
Where X is fraction of melt solidified, C0 is initial concentration, Cs is solid concentration. The below figure illustrates the segregation behavior of several segregation coefficients. It is found experimentally that segregation coefficients differ from equilibrium values and it is necessary to define effective segregation coefficient constant ke
Where V is pull rate, D is diffusion coefficient of dopant in the melt, B is stagnant layer thickness.