Abstract

Specular HgTe–CdTe superlattice epilayers have been obtained on two 2-in. diam GaAs or sapphire wafers per growth run using a horizontal metalorganic chemical vapor deposition (MOCVD) reactor in which the pyrolysis of the organometallics is induced by a cracking susceptor suspended above the substrates. This enables growth of superlattices below 300 °C using the standard precursors dimethyl cadmium, diethyl telluride, and elemental mercury. Annealing the superlattices at 350 °C converts them to homogeneous Hg1−xCdxTe. Compositional profiles obtained by Rutherford backscattering, sputter Auger depth profiling, and e-beam analysis of ultramicrotomed thin cross sections, were used to study interdiffusion of the CdTe and HgTe layers during growth and annealing. Arrays of metal–semiconductor field effect transistors (MESFETS) and photoconductive detectors with room temperature peak responsivity between 1.3 and 1.6 μm have been prepared from incompletely interdiffused material grown on semi-insulating GaAs without thick buffer layers. Device processing used mesa technology and a KI:I2:HBr etchant developed for its selectivity with respect to Hg1−xCdxTe . Capping layers of CdTe and HgTe deposited at low temperatures have been investigated as dielectric and ohmic contacts, respectively. Electrical analyses by Hall and C–V measurements are presented. Room temperature electron mobilities up to 27 500 cm2 /V s and resistivities of 1–2 Ω cm have been observed for the HgTe layers. Information on crystallinity and defect structure of the epilayers was obtained by selected area electron channeling patterns, high-resolution transmission electron microscopy (HRTEM), Rutherford backscattering spectroscopy (RBS) and four-circle, double-crystal, and triple-crystal x-ray diffraction. Compositional profiles in the 100 cm2 deposition area were obtained by wavelength dispersive x-ray analysis (WDX), Fourier transform infrared (FTIR) spectrometry and inductively coupled plasma atomic emission spectrometry (ICPAES).

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