Crystal Chemical Vapor Deposition Diamond Research Articles

Dynamics of charged and neutral silicon-vacancy color centers in electron-irradiated 28Si-doped single crystal chemical vapor deposition diamond upon annealing: Optical spectroscopy study

Diamond synthesis with silicon-vacancy (SiV) color centers is of high interest to nanophotonics and optical quantum technologies. The methods to control and/or maximize concentration of Si atoms incorporated in diamond lattice, and coupled to vacancies, together with improving crystallinity of diamond structure, are in demand. Here, we studied the effect of heat treatment of electron-irradiated single crystal CVD diamond doped with 28S isotope, on evolution of the neutral SiV0 and negatively charged SiV− centers. The crystal subjected to stepwise annealing at temperatures Tann from 200 °C to 1640 °C has been analyzed with photoluminescence (PL) and optical absorption spectroscopies at room and low-temperature (T = 5 K). We found a complex non-monotonous behavior of SiV0 and SiV− intensity both in absorption and PL, with sharp rise at Tann > 600 °C, reaching a maximum concentration peak, decline at 850 °C, and a repeated elevation to higher Tann, reflecting creation and annihilation processes of these defects. Moreover, we detected a group of seven lines of a Si-related defect in the range 828–871 nm, which strongly correlate with annealing dynamics of the SiV− and, especially, of SiV0 centers, and estimated the isotope spectral shift. In parallel, dynamics of other optical centers such as NV, R11 and GR1, in course of the annealing is traced. The controlled annealing opens the way to preparation of the SiV color centers with optimized optical properties, promising for quantum technologies.

Simultaneous measurements for fast neutron flux and tritium production rate using pulse shape discrimination and single crystal CVD diamond detector

This paper presents the development of a simultaneous measurement method for fast neutron energy spectra and tritium production rates within mixed radiation fields using a single crystal chemical vapour deposition diamond detector combined with a lithium fluoride (LiF) foil. The method involves the separation of pulses with rectangular shapes and the determination of the depth position within the single crystal diamond (SCD) struck by fast neutrons or nuclear reaction products including recoil tritons from the LiF foil based on pulse width, extracting pulse events occurred at the specific bulk region and the surface region of the SCD. Subsequently, unfolding techniques were employed to analyse the energy deposition spectrum of pulses at the specific bulk region which are induced only by fast neutrons, allowing the deduction of the fast neutron energy spectrum. To evaluate the tritium production rate, the energy deposition spectrum of pulses from events occurring at the SCD surface facing the LiF foil was analysed. By estimating the energy deposition spectrum solely induced by fast neutrons striking the SCD surface and subtracting it from the energy deposition spectrum of events at the SCD surface, the contribution of energetic ions, such as recoil tritons generated by the 6Li(n,α)3H reaction in the LiF foil, was determined. The fast neutron flux and tritium production rate obtained through this study were consistent with particle transport calculations, demonstrating the successful development of a method suitable for performance testing of fusion reactor blankets.

High temperature X-ray and γ-ray spectroscopy with a diamond detector

A single crystal chemical vapour deposition diamond detector was electrically characterised and then investigated as a spectroscopic photon counting X-ray and γ-ray detector across the temperature range, T, −20 °C ≤ T ≤ 100 °C. The detector was connected to a custom-built charge-sensitive preamplifier of low electronic noise and illuminated in turn by 55Fe radioisotope X-ray and 109Cd radioisotope X-ray and γ-ray sources. In combination, the radiation sources provided characteristic soft (e.g. 5.9 keV) and hard (e.g. 22.16 keV) X-rays and 88.03 keV γ-ray emissions. The Mn Kα (5.9 keV) and Kβ (6.49 keV) X-ray emissions from the 55Fe radioisotope X-ray source were detected (and separated from the zero energy noise peak) at temperatures of −20 °C ≤ T ≤ 60 °C; the Ag Kα (22.16 and 21.99 keV) and Kβ (24.94, 24.99, and 25.46 keV) X-ray emissions and 88.03 keV γ-ray emissions were detectable across the entire temperature range investigated (−20 °C ≤ T ≤ 100 °C). The detector and the preamplifier were operated without cooling across the entire temperature range. The energy resolution (full width at half maximum) at 22.16 keV (Ag Kα1) was 4.57 keV ± 0.26 keV at 100 °C and 2.70 keV ± 0.18 keV at −20 °C. Noise analysis indicated that the combination of dielectric noise and any incomplete charge collection noise present dominated the other noise components at 5.9 keV. When the detector was illuminated with the 109Cd radioisotope X-ray and γ-ray source, a high count rate introduced parasitic effects (possibly baseline shift) which reduced the optimum shaping time of the spectrometer.

Electron spectroscopy with a diamond detector

An electronic grade single crystal chemical vapour deposition diamond was investigated as a prototype high temperature spectroscopic electron (β- particle) detector for future space science instruments. The diamond detector was coupled to a custom-built charge-sensitive preamplifier of low noise. A 63Ni radioisotope source (endpoint energy 66 keV) was used to provide a spectrum of β- particles incident on the detector. The operating temperature of the detector/preamplifier assembly was controlled to allow its performance to be investigated between +100 °C and −20 °C, in 20 °C steps. Monte Carlo modelling was used to: a) calculate the β- particle spectrum incident on the detector; b) calculate the fraction of β- particle energy deposited into the detector; and c) predict the β- particle spectrum accumulated by the instrument. Comparison between the model and experimental data suggested that there was a 4.5 μm thick recombination region at the front of the detector. The spectrometer was demonstrated to be fully operable at temperatures, T, −20 °C ≤ T ≤ 80 °C; the results suggested that some form of polarisation phenomenon occurred in the detector at > 80 °C. This article presents the first report of an energy calibrated (≲ 50 keV) spectroscopic β- particle diamond detector.

Irradiated Single Crystal Chemical Vapor Deposition Diamond Characterized with Various Ionizing Particles

The radiation hardness of diamond at the sensor level is studied by irradiating five sensors and studying them with various particle sources, without making any modifications to the sensors in between. The electronics used in the characterization is not irradiated to ensure that any observed effect is merely due to the sensor. Three sensors have received a fluence of 1014 protons cm−2 and two 5⋅1015 protons cm−2. At the lower fluence, the impact on the charge collection efficiency is very small, when the applied bias voltage is above 1 V μm−1. For the higher fluence, the charge collection efficiency is lower than expected based on earlier studies of diamond radiation hardness on the substrate level. Furthermore, it is noticed that the irradiation has a stronger impact on the signal amplitude recorded with a fast timing than with a charge sensitive amplifier.

Large radius of curvature micro-lenses on single crystal diamond for application in monolithic diamond Raman lasers

The design and fabrication of large radii of curvature micro-lenses in single crystal chemical vapour deposition diamond is described. An optimised photoresist reflow process and low selectivity inductively coupled plasma etching are used to actualize a uniform array of micro-lenses with radii of curvature of 13mm or more and a high quality surface of a root-mean-square roughness of 0.18nm. The processes developed have the potential to achieve diamond micro-lenses with an even larger radius of curvature. These new diamond micro-lenses enable the pulse energy scalable monolithic diamond Raman laser where a large radius of curvature of the micro-lenses is critical.

Radiation quality and ion-beam therapy: understanding the users' needs.

Ion-beam therapy faces a growing demand of tools able to map radiation quality within the irradiated volume. Although analytical computations and simulations provide useful estimations of dose and radiation quality, the direct measure of those parameters would improve ion-beam therapy in particular when deep-seated tumours are irradiated, tissue composition and density are variable or organs at risk are near the tumour. Several ion-beam therapy facilities are studying detectors and procedures for measuring the radiation quality on a microdosimetric as well as a nanodosimetric scale. Simplicity and miniaturisation of the devices are essential for measurements first in phantoms and thereafter during therapy, particularly for intra-cavity detectors. MedAustron is studying solid-state detectors based on a single crystal chemical vapour deposition diamond. In collaboration with Italian National Institute for Nuclear Physics (INFN), Tor Vergata and Legnaro; INFN-microdosimetry and track structure project; Austrian Institute of Technology, Vienna; and Italian National agency for new technologies, energy and sustainable economic development, Rome, prototypes have been developed to characterise radiation quality in sizes equivalent to one micrometre of biological tissue.

Long-lived NV− spin coherence in high-purity diamond membranes

The electronic spin associated with the nitrogen vacancy (NV) color center in diamond is an excellent candidate for a solid-state qubit functioning as a quantum register or sensor. However, the lack of thin film technologies for crystalline diamond with low impurity levels hampers the development of photonic interfaces to such diamond-based qubits. We present a method for manufacturing slabs of diamond of 200 nm thickness and several microns in extent from high-purity single crystal chemical vapor deposition diamond. We measure spin coherence times approaching 100 μs and observe increased photoluminescence collection from shallow implant NV centers in these slabs. We anticipate these slabs to be appealing as quantum memory nodes in hybrid diamond nanophotonic systems.

Monte Carlo simulations of multiplexed electronic grade CVD diamond for neutron detection

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.

CVD diamond sensor for UV-photon detection

A new generation of UV photosensors, based on single crystal Chemical Vapour Deposition (CVD) diamonds to work optically coupled with large volume two-phase liquid-Ar (LAr) or liquid-Xe (LXe) detectors nowadays under design for the next generation of WIMPs experiments, is under development. Preliminary tests and first calibrations show these devices can have better performance than the existing UV sensitive detectors (higher photosensitivity and better signal-to-noise ratio). I–V characteristics, dark current measurements, linearity response to X-ray irradiation, and α-particle energy resolution are reported and discussed.

Characterization of damage induced by heavy neutron irradiation on multilayered L6iF-single crystal chemical vapor deposition diamond detectors

High performance neutron detectors sensitive to both thermal and fast neutrons are of great interest to monitor the high neutron flux produced, e.g., by fission and fusion reactors. An obvious requirement for such an application is neutron irradiation hardness. This is why diamond based neutron detectors are currently under test in some of these facilities. In this paper the damaging effects induced in chemical vapor deposition (CVD) diamond based detectors by a neutron fluence of ∼2×1016 neutrons/cm2 have been studied and significant changes in spectroscopic, electrical, and optical properties have been observed. The detectors are fabricated using high quality synthetic CVD single crystal diamond using the p-type/intrinsic/Schottky metal/L6iF layered structure recently proposed by Marinelli et al. [Appl. Phys. Lett. 89, 143509 (2006)], which allows simultaneous detection of thermal and fast neutrons. Neutron radiation hardness up to at least 2×1014 n/cm2 fast (14 MeV) neutron fluence has been confirmed so far [see Pillon et al., (Fusion Eng. Des. 82, 1174 (2007)]. However, at the much higher neutron fluence of ∼2×1016 neutrons/cm2 damage is observed. The detector response to 5.5 MeV A241m α-particles still shows a well resolved α-peak, thus confirming the good radiation hardness of the device but a remarkable degradation and a significant instability with time of charge collection efficiency and energy resolution arise. Symmetric, nearly Ohmic I-V (current-voltage) characteristics have been recorded from the metal/intrinsic/p-doped diamond layered structure, which before neutron irradiation acted as a Schottky barrier diode with a strong rectifying behavior. The nature and the distribution of the radiation induced damage have been deeply examined by means of cathodoluminescence spectroscopy. A more heavily damaged area into the intrinsic diamond at the same position and with the same extension of the L6iF layer has been found, the increased damage being ascribed to the highly ionizing particles produced in the L6iF layer by thermal neutrons through the nuclear reaction L6i(n,α)T.

Radiation tolerance of a high quality synthetic single crystal chemical vapor deposition diamond detector irradiated by 14.8 MeV neutrons

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 A241m 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.

Investigations of high mobility single crystal chemical vapor deposition diamond for radiotherapy photon beam monitoring

The intrinsic properties of diamond make this material theoretically very suitable for applications in medical physics. Until now ionization chambers have been fabricated from natural stones and are commercialized by PTW, but their fairly high costs and long delivery times have often limited their use in hospital. The properties of commercialized intrinsic polycrystalline diamond were investigated in the past by many groups. The results were not completely satisfactory due to the nature of the polycrystalline material itself. In contrast, the recent progresses in the growth of high mobility single crystal synthetic diamonds prepared by chemical vapor deposition (CVD) technique offer new alternatives. In the framework of the MAESTRO project (Methods and Advanced Treatments and Simulations for Radio Oncology), the CEA-LIST is studying the potentialities of synthetic diamond for new techniques of irradiation such as intensity modulated radiation therapy. In this paper, we present the growth and characteristics of single crystal diamond prepared at CEA-LIST in the framework of the NoRHDia project (Novel Radiation Hard CVD Diamond Detector for Hadrons Physics), as well as the investigations of high mobility single crystal CVD diamond for radiotherapy photon beam monitoring: dosimetric analysis performed with the single crystal diamond detector in terms of stability and repeatability of the response signal, signal to noise ratio, response speed, linearity of the signal versus the absorbed dose, and dose rate. The measurements performed with photon beams using radiotherapy facilities demonstrate that single crystal CVD diamond is a good alternative for air ionization chambers for beam quality control.

Status of diamond detectors and their high energy physics application

Particle physics collider experiments at the high energy frontier are being performed today and in the next decade in increasingly harsh radiation environments. New radiation hard technologies, such as particle detectors based on diamond, must be developed. This paper discusses the use of diamond detectors in tracking and beam condition monitoring applications and their survivability in the highest radiation environments. This paper presents recent results of devices based on polycrystalline and single crystal Chemical Vapor Deposition diamond and their tolerance to radiation.

Radiation hard diamond sensors for future tracking applications

Progress in experimental particle physics in the coming decade depends crucially upon the ability to carry out experiments in high-radiation areas. In order to perform these complex and expensive experiments, new radiation hard technologies must be developed. This paper discusses the use of diamond detectors in future tracking applications and their survivability in the highest radiation environments. We present results of devices constructed with the newest polycrystalline and single crystal Chemical Vapor Deposition diamond and their tolerance to radiation.

Calibration of National Ignition Facility neutron detectors in the energy range E<14 MeV

We examine various options for calibration of the National Ignition Facility neutron detectors in the energy range E<14 MeV. These options include: downscatter of D–T fusion neutrons using plastic targets; nuclear reactions at a Tandem Van de Graaf accelerator; and “white” neutrons from a pulsed spallation source. As an example of the pulsed spallation option, we present calibration data that was recently acquired with a single crystal chemical vapor deposition diamond detector at the Weapons Neutron Research Facility at Los Alamos National Laboratory.

A neutron sensor based on single crystal CVD diamond

We report the first neutron data for a single crystal Chemical Vapor Deposition diamond sensor. Results are presented for 2.5, 14.1, and 14.9 MeV incident neutrons. We show that the energy resolution for 14.1 MeV neutrons is at least 2.9% (as limited by the energy spread of the incident neutrons), and perhaps as good as 0.4% (as extrapolated from high resolution α-particle data). This result could be relevant to fusion neutron spectroscopy at machines like the International Thermonuclear Experimental Reactor. We also show that our sensor has a high neutron linear attenuation coefficient, due to the high atomic density of diamond, and this could lead to applications in fission neutron detection.