Method of forming epitaxial layers

Claim 3

A method as claimed in claim 1, characterized in that the lower epitaxial layer is made of gallium indium arsenide having the formula Ga 0 .47 In 0 .53 As and the upper layer is made of indium phosphide (InP).

Claim 4

A method as claimed in claim 1, characterized in that the lower epitaxial layer is made of gallium indium arsenide (Ga In As), the upper epitaxial layer is made of indium phosphide (InP) and gaseous indium chloride (In Cl) is employed to provide the maximum coverage rate with chlorine (Cl) atoms.

Claim 5

A method as claimed in claim 3, characterized in that the deposition temperature T D is considered to be low in the range of from 600° to 640° C., the reacting molar fraction of InCl is considered to be large in the range of from 2.10 -3 to 4.10 -3 and the parameters deposition temperature T D and molar fraction of InCl during the deposition of the indium phosphide (InP) are chosen in these ranges whilst taking into account the fact that these parameters cooperate in inverse ratio to each other.

Claim 6

A method as claimed in claim 4, characterized in that the molar fraction of InCl is chosen equal to 2.7·10 -3 .

Claim 7

A method as claimed in claim 5, characterized in that the deposition temperature T D is chosen equal to 620° C.

Claim 8

A method as claimed in claim 6, characterized in that the sources required to carry out the deposition from the chloride vapor phase first comprise an arsenic trichloride (AsCl 3 ) liquid bubbler (31) and a phosphorus trichloride (PCl 3 ) liquid bubbler (21) brought to a temperature sufficiently high so that flows of hydrogen introduced into these liquid bubblers (31, 33) take along quantities of AsCl 3 and PCl 3 material, respectively, which are decomposed and then react on solid sources designated as first and second sources, respectively (21), of gallium arsenide (GaAs) of indium and indium phosphide (InP) brought to a temperature T S higher than the deposition temperature T D , from which reactions become available gallium chloride (GaCl)+As and indium chloride (InCl) P4, respectively, the the gaseous state, and comprise an arsenic chloride (AsCl 3 ) liquid bubbler (32) brought to a temperature sufficiently high so that a flow of hydrogen introduced into this liquid bubbler (32) take as along a quantity of arsenic chloride which is decomposed to produce gaseous hydrochloride HCl, which is taken to a source of liquid indium (22) designated as third source brought to a temperature T S , and from which reaction there becomes available gaseous indium chloride (InCl), and in that, in order to obtain the molar fraction of InCl required, the product of the third source is introduced simultaneously with the product of the first source (21) for processing the layer of gallium indium arsenide (GaInAs), while the product of the third source (22) is introduced simultaneously with the product of the second source (23) for processing the layer of indium phosphide (InP).

Claim 9

A method as claimed in claim 7, characterized in that the temperature of the sources T S is 80° to 100° C. higher than the deposition temperature T D .

Claim 10

A method as claimed in claim 8, characterized in that the layers of gallium indium arsenide (GaInAs) and of indium phosphide (InP), respectively, are deposited on a substrate of indium phosphide (InP), and in that the ratio between the partial pressure of indium chloride and the partial pressure of gallium chloride is chosen so as to obtain layers of gallium arsenide of the composition Ga 0 .47 In 0 .53 As permitting of obtaining lattice matching with the substrate.

Claim 11

A method as claimed in claim 2, characterized in that the operating conditions include for obtaining a high rate of coverage with chlorine (Cl) of the layer of GaInAs a low deposition temperature T D of the layer and for obtaining a high rate of coverage with chlorine (Cl) of the layer of InP a large molar fraction of indium chloride MF(InCl) during the formation of the layer of InP.