Recently, solid state photovoltaic Schottky diodes, able to detect ionizing radiation, in particular, x-ray and ultraviolet radiation, have been developed at the University of Rome “Tor Vergata.” We report on a physical and electrical properties analysis of the device and a detailed study of its detection capabilities as determined by its electrical properties. The design of the device is based on a metal/nominally intrinsic/p-type diamond layered structure obtained by microwave plasma chemical vapor deposition of homoepitaxial single crystal diamond followed by thermal evaporation of a metallic contact. The device can operate in an unbiased mode by using the built-in potential arising from the electrode-diamond junction. We compare the expected response of the device to photons of various energies calculated through Monte Carlo simulation with experimental data collected in a well controlled experimental setup i.e., monochromatic high flux x-ray beams from 6 to 20 keV, available at the Diamond Light Source synchrotron in Harwell (U.K.).

High-quality single-crystal diamond films, homoepitaxially grown by microwave chemical vapor deposition, have been used to produce diamond-based photodetectors. Such devices were tested over a very wide spectral range, from the extreme ultraviolet (UV) (20 nm) up to the near IR region (2400 nm). An optical parametric oscillator tunable laser was used to investigate the 210-2400 nm spectral range in pulse mode. In this region, the spectral response shows a UV to visible contrast of about 6 orders of magnitude. A time response shorter than 5 ns, i. e., the laser pulse duration, was observed. By integrating the pulse shape, a minor slow component was evidenced, which can be explained in terms of trapping-detrapping effects. Extreme UV gas sources and a toroidal grating vacuum monochromator were used to measure the device response down to 20 nm in continuous mode. In particular, the extreme UV He spectrum was measured and the He II m, 30.4 nm and He I 58.4 nm emission lines were clearly detected. The measured time response of 0.2 s is totally due to the instrumental readout time constants. In both experimental setups an extremely good stability and reproducibility of the device response were obtained, whereas no persistent photoconductivity nor undesirable pumping effects were observed

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Fabrication reproducibility and high performance reliability were obtained in fissile-material-free thermal neutron detectors based on chemical vapor deposited diamond in a multilayered p-type/intrinsic/metal design. Under α particle irradiation, all the detectors (more than ten) have shown 100% charge collection efficiency and approximately 1.5% energy resolution. A Li6F layer was deposited on the detector surface as converting material for thermal neutrons through the Li6(n,α)T nuclear reaction. Both the 2.73MeV tritium and the 2.06MeV α peaks are detected and clearly resolved. Stable performance and excellent linear behavior of the count rate versus the incident neutron flux were observed.

Thermal neutron flux monitors were fabricated using chemical vapor deposited single crystal diamond in a p-type/intrinsic/metal/⁶LiF layered structure. They were placed 80 cm above the core midplane of a 1 MW research fission reactor, where the maximum neutron flux is 2.2×10⁹ neutrons/cm² s. Good stability and reproducibility of the device response were observed over the whole reactor power range. A 150 000 counts/s count rate was measured at the maximum reactor power with no degradation of the detector signal. As the multiple pile-up process due to the slow readout electronics is accounted for, an excellent linearity of the diamond response is observe

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Recently, a compact solid-state neutron detector capable of simultaneously detecting thermal and fast neutrons was proposed [M. Marinelli et al., Appl. Phys. Lett. 89, 143509 (2006)]. Its design is based on a p-type/intrinsic/metal layered structure obtained by Microwave Plasma Chemical Vapor Deposition (CVD) of homoepitaxial diamond followed by thermal evaporation of an Al contact and a ⁶LiF converting layer. Fast neutrons are directly detected in the CVD diamond bulk, since they have enough energy to produce the ¹²C(n, α)⁹Be reaction in diamond. Thermal neutrons are instead converted into charged particles in the ⁶LiF layer through the ⁶Li(n, α)T nuclear reaction. These charged particles are then detected in the diamond layer. The thickness of the ⁶LiF converting layer and the CVD diamond sensing layer affect the counting efficiency and energy resolution of the detector both for low- (thermal) and high-energy neutrons. An analysis is carried out on the dynamics of the ⁶Li(n, α)T and the ¹²C(n, α)⁹Be reactions products, and the distribution of the energy released inside the sensitive layer is calculated. The detector counting efficiency and energy resolution were accordingly derived as a function of the thickness of the ⁶LiF and CVD diamond layers, both for thermal and fast neutrons, thus allowing us to choose the optimum detector design for any particular application. Comparison with experimental results is also reported

Diamond exhibits many properties such as an outstanding radiation hardness and fast response time both important to design detectors working in extremely radioactive environments. Among the many applications these devices can be used for, there is the development of a fast and radiation hard neutron detector for the next generation of fusion reactors, such as the International Thermonuclear Experimental Reactor project, under construction at Cadarache in France. A technology to routinely produce electronic grade synthetic single crystal diamond detectors was recently developed by our group. One of such detectors, with an energy resolution of 0.9% as measured using an ²⁴¹Am α particle source, has been heavily irradiated with 14.8 MeV neutrons produced by the Frascati Neutron Generator. The modifications of its spectroscopic properties have been studied as a function of the neutron fluence up to 2.0×10¹⁴ n/cm². In the early stage of the irradiation procedure an improvement in the spectroscopic performance of the detector was observed. Subsequently the detection performance remains stable for all the given neutron fluence up to the final one thus assessing a remarkable radiation hardness of the device. The neutron damage in materials has been calculated and compared with the experimental results. This comparison is discussed within the nonionizing energy loss (NIEL) hypothesis, which states that performance degradation is proportional to NIEL