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   <subfield code="a">History of the &quot;Detector Materials Engineering” Crystal Growth Process for Bulk Hg1− x Cd x Te</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[W. Higgins, D. Nelson, R. Roy, R. Murosako, R. Lancaster, J. Tower, P. Norton]</subfield>
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   <subfield code="a">This paper reviews the history and technology of a bulk Hg1−x Cd x Te crystal growth process that was developed in the early 1980s at Honeywell Electro-Optics Division (presently BAE Systems, Electronic Solutions). The crystal growth process name, DME, was an acronym for the department name: Detector Materials Engineering. This was an accelerated crucible rotation technique (ACRT) vertical traveling heater method growth process. Crystal growth occurred in the pseudobinary Hg1−x Cd x Te system. ACRT mixing allowed the lower-density, higher-x-value Hg1−x Cd x Te growth nutrient in the upper region of the ampoule to replenish the depleted melt and allowed the growth of constant-x-value, higher-density Hg1−x Cd x Te. The material grown by this research and production growth process yielded single crystals that had improved purity, compositional uniformity, precipitate density, and reproducibility in comparison with solid-state recrystallization and other bulk Hg1−x Cd x Te growth techniques. Radial and longitudinal nonuniformities in x-value for Hg1−x Cd x Te were reduced to &lt;0.0008/cm. The net electrically active background impurities did not exceed 1×1014cm−3. Electron mobilities in excess of 1.5×106cm2/V-s were observed at 77K. Structural defects of less than 104cm−2 were measured. Te precipitates were not observed. As a result of these material improvements, long-wavelength infrared (LWIR) photoconductive devices fabricated from DME material had highly desired performance characteristics.</subfield>
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