Abstract

Abstract A novel and evolutionary multiplexing technique is introduced in this work where electronic grade single crystal chemical vapor deposition (CVD) diamond plates are multiplexed together in both a series and parallel configuration, sending electronic signals from each diamond plate to a single electronic acquisition system. Modeling of this novel multiplexing technique consisted of MCNPX simulations and significant post processing. The model developed allowed for the characterization of charge collection efficiency corrections to the location of charge creation to determine the effect of increasing detection medium size with respect to charge collection direction on the measured pulse height spectrum. This work was conducted to show that this technique is theoretically capable of replacing a single crystal diamond plate of similar size for use in neutron detection without the immediate need of advancing CVD diamond growth technologies. Further, this work indicates the expected pulse height evolution from a singular large single crystal diamond if such a crystal is produced in the future. The results of this work indicate that a 14.1 MeV neutron induced energy pulse of 8.4 MeV (due to the 12C(n,αo)9Be reaction) in the pulse height spectrum has its energy resolution broadened by a factor of two to a total value of 0.225 percent for a multiplexed array with a thickness from 0.05 to 1 cm and an intrinsic detection efficiency of 25.4 percent for a 1 cm thick diamond crystal. It is also qualitatively discussed that the number of secondary neutron interactions with the diamond detector array may be about 5 percent. The results of this work indicate the capability of multiplexing diamond plates together for spectroscopic neutron detection with a combined intrinsic detection efficiency and energy resolution greater than any other diamond-based neutron detection system reported to date.

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