Mechanisms of H release from Mg-doped, p-type GaN were investigated in vacuum, in N{sub 2} and O{sub 2} gases, and in electron-cyclotron-resonance N{sub 2} plasmas. Replacing grown-in protium with deuterium (D) and employing sensitive nuclear-reaction analysis allowed the retained concentration to be followed quantitatively over two decades during isothermal heating, illuminating the kinetics of controlling processes. Oxidation attending the O{sub 2} exposures was monitored through nuclear-reaction analysis of {sup 18}O. N{sub 2} gas at atmospheric pressure increases the rate of D release appreciably relative to vacuum. The acceleration produced by O{sub 2} gas is much greater, but is diminished in later stages of the release by oxidation. The N{sub 2} plasma employed in these studies had no resolvable effect. We argue that surface desorption is rate controlling in the D release, and that it occurs by D-D recombination and the formation of N-D and O-D species. Our results are quantitatively consistent with a theoretical model wherein the bulk solution is in equilibrium with surface states from which desorption occurs by processes that are both first and second order in surface coverage.
Proposed next-step devices for development of fusion energy present a major increase in the energy content and duration of plasmas far beyond those encountered in existing machines. This increases the importance of controlling interactions between the fusion plasma and first-wall materials. These interactions change the wall materials and strongly affect the core plasma conditions. Two critical processes are the erosion of materials by the plasma, and the redeposition of eroded material along with hydrogen isotopes from the plasma. These impact reactor design through the lifetime of plasma-facing components and the inventory of tritium retained inside the vessel. Ion beam analysis has been widely used to investigate these complex plasma-material interactions in most of the large fusion plasma experiments. The design and choice of plasma-facing materials for next-step machines rely on knowledge obtained from these studies. This paper reviews the use of ion beam analysis for fusion energy research, and shows how these studies have helped to guide the design and selection of materials for a next-step machine.
This report documents the strategies for verification and validation of the codes LSP and ICARUS used for simulating the operation of the neutron tubes used in all modern nuclear weapons. The codes will be used to assist in the design of next generation neutron generators and help resolve manufacturing issues for current and future production of neutron devices. Customers for the software are identified, tube phenomena are identified and ranked, software quality strategies are given, and the validation plan is set forth.
This LDRD is aimed to place Sandia at the forefront of GaN-based technologies. Two important themes of this LDRD are: (1) The demonstration of novel GaN-based devices which have not yet been much explored and yet are coherent with Sandia's and DOE's mission objectives. UV optoelectronic and piezoelectric devices are just two examples. (2) To demonstrate front-end monolithic integration of GaN with Si-based microelectronics. Key issues pertinent to the successful completion of this LDRD have been identified to be (1) The growth and defect control of AlGaN and GaN, and (2) strain relief during/after the heteroepitaxy of GaN on Si and the separation/transfer of GaN layers to different wafer templates.
The diffusion, uptake, and release of H in p-type GaN are modeled employing state energies from density-function theory and compared with measurements of deuterium uptake and release using nuclear-reaction analysis. Good semiquantitative agreement is found when account is taken of a surface permeation barrier.
The ability to withstand disruptions makes carbon-based materials attractive for use as plasma-facing components in divertors. However, such materials suffer high erosion rates during attached plasma operation which, in high power long pulse machines, would give short component lifetimes and high tritium inventories. The authors present results from recent experiments in DIII-D, in which the Divertor Materials Evaluation System (DiMES) was used to examine erosion and deposition during short exposures to well defined plasma conditions. These studies show that during operation with detached plasmas, produced by gas injection, net erosion is suppressed everywhere in the divertor. Net deposition of carbon with deuterium was observed at the inner and outer strikepoints and in the private-flux region between strikepoints. For these low temperature plasmas (T{sub e} < 2eV), physical sputtering is eliminated. These results show that with detached plasmas, the location of carbon net erosion and the carbon impurity source, probably lies outside the divertor. Physical or chemical sputtering by charge-exchange neutrals or ions in the main plasma chamber is a probable source of carbon under these plasma conditions.
The National Spherical Torus Experiment (NSTX) started plasma operations in February 1999, and promptly achieved high current, inner wall limited, double null, and single null plasma discharges, initial Coaxial Helicity Injection, and High Harmonic Fast Wave results. NSTX is designed to study the physics of Spherical Tori (ST) in a device that can produce non-inductively sustained high-{beta} discharges in the 1 MA regime and to explore approaches toward a small, economical high power density ST reactor core. As expected, discharge reproducibility and performance were strongly affected by wall conditions. In this paper, the authors describe the internal geometry, and initial plasma discharge, impurity control, wall conditioning, erosion, and deposition results.
Formation energies and vibrational frequencies for H in wurtzite GaN were calculated from density functional theory and used to predict equilibrium state occupancies and solid solubilities for p-type, intrinsic, and n-type material. The solubility of deuterium (D) was measured at 600--800 C as a function of D{sub 2} pressure and doping and compared with theory. Agreement was obtained by reducing the H formation energies 0.2 eV from ab-initio theoretical values. The predicted stretch-mode frequency for H bound to the Mg acceptor lies 5% above an observed infrared absorption attributed to this complex. It is concluded that currently recognized H states and physical processes account for the equilibrium behavior of H examined in this work.
The behavior of H in p-GaN(Mg) at temperatures >400 C is modeled by using energies and vibrational frequencies from density-functional theory to parameterize transport and reaction equations. Predictions agree semiquantitatively with experiment for the solubility, uptake, and release of the H when account is taken of a surface barrier. Hydrogen is introduced into GaN during growth by metal-organic chemical vapor deposition (MOCVD) and subsequent device processing. This impurity affects electrical properties substantially, notably in p-type GaN doped with Mg where it reduces the effective acceptor concentration. Application of density-functional theory to the zincblende and wurtzite forms of GaN has indicated that dissociated H in interstitial solution assumes positive, neutral, and negative charge states. The neutral species is found to be less stable than one or the other of the charged states for all Fermi energies. Hydrogen is predicted to form a bound neutral complex with Mg, and a local vibrational mode ascribed to this complex has been observed. The authors are developing a unified mathematical description of the diffusion, reactions, uptake, and release of H in GaN at the elevated temperatures of growth and processing. Their treatment is based on zero-temperature energies from density functional theory. One objective is to assess the consistency of theory with experiment at a more quantitative level than previously. A further goal is prediction of H behavior pertinent to device processing. Herein is discussed aspects relating to p-type GaN(Mg).
The authors have used ion channeling to examine the lattice configuration of deuterium in Mg doped GaN grown by MOCVD. The deuterium is introduced both by exposure to deuterium gas and to ECR plasmas. A density functional approach including lattice relaxation, was used to calculate total energies for various locations and charge states of hydrogen in the wurtzite Mg doped GaN lattice. Computer simulations of channeling yields were used to compare results of channeling measurements with calculated yields for various predicted deuterium lattice configurations.
A technique has been developed for producing calibrated metal hydride films for use in the measurement of high-energy (5--15 MeV) particle reaction cross sections for hydrogen and helium isotopes on hydrogen isotopes. Absolute concentrations of various hydrogen isotopes in the film is expected to be determined to better than {+-}2% leading to the capacity of accurately measuring various reaction cross sections. Hydrogen isotope concentrations from near 100% to 5% can be made accurately and reproducibly. This is accomplished with the use of high accuracy pressure measurements coupled with high accuracy mass spectrometric measurements of each constituent partial pressure of the gas mixture during loading of the metal occluder films. Various techniques are used to verify the amount of metal present as well as the amount of hydrogen isotopes; high energy ion scattering analysis, PV measurements before, during and after loading, and thermal desorption/mass spectrometry measurements. The most appropriate metal to use for the occluder film appears to be titanium but other occluder metals are also being considered. Calibrated gas ratio samples, previously prepared, are used for the loading gas. Deviations from this calibrated gas ratio are measured using mass spectrometry during and after the loading process thereby determining the loading of the various hydrogen isotopes. These techniques are discussed and pertinent issues presented.
We estimate the total in-vessel deuterium retention in Alcator C-Mod from a run campaign of about 1090 plasmas. The estimate is based on measurements of deuterium retained on 22 molybdenum tiles from the inner wall and divertor. The areal density of deuterium on the tiles was measured by nuclear reaction analysis. From these data, the in-vessel deuterium inventory is estimated to be about 0.1 gram, assuming the deuterium coverage is toroidally symmetric. Most of the retained deuterium is on the walls of the main plasma chamber, only about 2.5% of the deuterium is in the divertor. The D coverage is consistent with a layer saturated by implantation with ions and charge-exchange neutrals from the plasma. This contrasts with tokamaks with carbon plasma-facing components (PFC's) where long-term retention of tritium and deuterium is large and mainly in the divertor due to codeposition with carbon eroded by the plasma. The low deuterium retention in the C-Mod divertor is mainly due to the absence of carbon PFC's in C-Mod and the low erosion rate of Mo.
This section reviews physical processes involved in the implantation of energetic hydrogen into plasma facing materials and its subsequent diffusion, release, or immobilization by trapping or precipitation within the material. These topics have also been discussed in previous reviews. The term hydrogen or H is used here generically to refer to protium, deuterium or tritium.
Tungsten is a candidate material for the International Thermonuclear Experimental Reactor (ITER) as well as other future magnetic fusion energy devices. Tungsten is well suited for certain fusion applications in that it has a high threshold for sputtering as well as a very high melting point. As with all materials to be used on the inside of a tokamak or similar device, there is a need to know the behavior of hydrogen isotopes embedded in the material. With this need in mind, the Tritium Plasma Experiment (TPE) has been used to examine the retention of tritium in tungsten exposed to high fluxes of 100 eV tritons. Both tungsten and tungsten containing 1% lanthanum oxide were used in these experiments. Measurements were performed over the temperature range of 423-973 K. After exposure to the tritium the samples were transferred to an outgassing system containing an ionization chamber for detection of the tritium. The samples were outgassed using linear ramps from room temperature up to 1473 K. Unlike most other materials exposed to energetic tritium, the tritium retention in tungsten reaches a maximum at intermediate with low retention at both high and low temperatures. For the very high triton fluences used (>1025 T/m2), the fractional retention of the tritium was below 0.02% of the incident particles. This report presents not only the results of the tritium retention, but also includes the modeling of the results and the implication for ITER and other future fusion devices where tungsten is used.
The International Thermonuclear Experimental Reactor (ITER) is envisioned to be the next major step in the world`s fusion program from the present generation of tokamaks and is designed to study fusion plasmas with a reactor relevant range of plasma parameters. During normal operation, it is expected that a fraction of the unburned tritium, that is used to routinely fuel the discharge, will be retained together with deuterium on the surfaces and in the bulk of the plasma facing materials (PFMs) surrounding the core and divertor plasma. The understanding of he basic retention mechanisms (physical and chemical) involved and their dependence upon plasma parameters and other relevant operation conditions is necessary for the accurate prediction of the amount of tritium retained at any given time in the ITER torus. Accurate estimates are essential to assess the radiological hazards associated with routine operation and with potential accident scenarios which may lead to mobilization of tritium that is not tenaciously held. Estimates are needed to establish the detritiation requirements for coolant water, to determine the plasma fueling and tritium supply requirements, and to establish the needed frequency and the procedures for tritium recovery and clean-up. The organization of this paper is as follows. Section 2 provides an overview of the design and operating conditions of the main components which define the plasma boundary of ITER. Section 3 reviews the erosion database and the results of recent relevant experiments conducted both in laboratory facilities and in tokamaks. These data provide the experimental basis and serve as an important benchmark for both model development (discussed in Section 4) and calculations (discussed in Section 5) that are required to predict tritium inventory build-up in ITER. Section 6 emphasizes the need to develop and test methods to remove the tritium from the codeposited C-based films and reviews the status and the prospects of the most attractive techniques. Section 7 identifies the unresolved issues and provides some recommendations on potential R and D avenues for their resolution. Finally, a summary is provided in Section 8.
Net erosion rates of carbon target plates have been measured in situ for the DIII-D lower divertor. The principal method of obtaining this data is the DiMES sample probe. Recent experiments have focused on erosion at the outer strike-point of two divertor plasma conditions: (1) attached (Te > 40 eV) ELMing plasmas and (2) detached (Te < 2 eV) ELMing plasmas. The erosion rates for the attached cases are > 10 cm/year, even with incident heat flux < 1 MW/m{sup 2}. In this case, measurements and modeling agree for both gross and net carbon erosion, showing the near-surface transport and redeposition of the carbon is well understood and that effective sputtering yields are > 10%. In ELM-free discharges, this erosion rate can account for the rate of carbon accumulation in the core plasma. Divertor plasma detachment eliminates physical sputtering, while spectroscopically measured chemical erosion yields are also found to be low (Y(C/D{sup +}) {le} 2.0 {times} 10{sup {minus}3}). This leads to suppression of net erosion at the outer strike-point, which becomes a region of net redeposition ({approximately} 4 cm/year). The private flux wall is measured to be a region of net redeposition with dense, high neutral pressure, attached divertor plasmas. Leading edges intercepting parallel heat flux ({approximately} 50 MW/m{sup 2}) have very high net erosion rates ({approximately} 10 {micro}m/s) at the OSP of an attached plasma. Leading edge erosion, and subsequent carbon redeposition, caused by tile gaps can account for half of the deuterium codeposition in the DIII-D divertor.
The mission of the Divertor Materials Evaluation System (DiMES) in DIII-D is to establish an integrated data base from measurements in the divertor of a tokamak in order to address some of the ITER and fusion power reactor plasma material interaction issues. Carbon and metal coatings of Be, W, V, and Mo were exposed to the steady-state outer strike point on DIII-D for 4--18 s. These short exposure times ensure controlled exposure conditions, and the extensive arrays of DIII-D divertor diagnostics provide a well-characterized plasma for modeling efforts. Post-exposure analysis provides a direct measure of surface material erosion rates and the amount of retained deuterium. For carbon, these results match closely with the results of accumulated carbon deposition and erosion, and the corresponding deuterium retention of long term exposure tiles in DIII-D. Under the carbon-contaminated background plasma of DIII-D, metal coatings of Be, V, Mo, and W were exposed to the steady-state outer strike point under ELMing and ELM-free H-mode discharges. The rate of material erosion and deuterium retention were measured. As expected, W shows the lowest erosion rate at 0.1 mm/s and the lowest deuterium uptake of 2 {times} 10{sup 20}/m{sup 2}.
The results of the investigation of retention and thermal desorption of hydrogen isotopes of B{sub 4}C coated RGT (a recrystallized graphite with high thermal conductivity, 600 W/mK) after the exposure to high heat flux in the divertor strike point region of DIII-D using the DiMES sample exchange system are reported. It is shown that the material is very promising for plasma facing elements of tokamaks.
Efficient techniques for rapid tritium removal will be necessary for ITER to meet its physics and engineering goals. One potential technique is transient surface heating by a scanning CO{sub 2} or Nd:Yag laser that would release tritium without the severe engineering difficulties of bulk heating of the vessel. The authors have modeled the heat propagation into a surface layer and find that a multi-kW/cm{sup 2} flux with an exposure time of order 10 ms is suitable to heat a 50 micron co-deposited layer to 1,000--2,000 degrees. Improved wall conditioning may be a significant side benefit. They identify remaining issues that need to be addressed experimentally.
Tritium retention and removal are critical issues for the success of ITER or any DT fusion reactor. The Tokamak Fusion Test Reactor, TFTR, is the first fusion facility to afford the opportunity to study the tritium retention and removal over an extended period. In TFTR, tritium accumulates on all surfaces with line of sight to the plasma by codeposition of tritium with carbon. Measurements of both deuterium and tritium retention fractions have yielded retention between 0.2 and 0.6 of the injected fuel in the torus. Tritium has been successfully removed from TFTR by glow discharge cleaning and by air purges. The in-vessel inventory was reduced by a factor of 2, facilitating machine maintenance. In TFTR, the amount of dust recovered from the TFTR vacuum vessel has varied from several grams to a few kilograms.
In applications dealing with the deposition of amorphous hydrogenated carbon layers or in the determination of the composition of deposited layers on the walls of nuclear fusion plasma experiments, the analysis of mixtures of light elements on heavy substrates is necessary. Depth profiling by means of RBS is often difficult due to the overlap of the backscattering intensities of different constituents from different depths. The erosion and reaction of deposited amorphous deuterated carbon (a-C:D) films with a Be substrate due to annealing in air poses an analytical challenge especially if simultaneously the exchange of hydrogen isotopes should be monitored. The analysis of the different recoiling atoms from collisions with heavy ions in Elastic Recoil Detection (ERD) can provide a tool which resolves all constituents in a single analysis. In the present study the composition of intermixed layers on Be containing H, D, Be, C and O has been analyzed using conventional {sup 4}He RBS at 2.2 MeV together with 2.5 MeV {sup 4}He ERD for hydrogen isotope analysis. At these energies, an overlap of signals from different constituents could be avoided in most cases. As alternative method heavy ion ERD using Si{sup 7+} ions extracted from a 5 MeV Tandem Van de Graff accelerator was investigated. At a scattering angle of 30{degree} Si ions could not be scattered into the detector and a solid state detector without protecting foil could be used. Even in the intermixed layers at terminal energies of 5 MeV the heavy constituents could be separated while signals from recoiling hydrogen and deuterium atoms could be resolved on top of the signal from the Be substrate. For the analysis of the RBS and ERD data the newly developed spectra simulation program SIMNRA has been used which includes a large data bank for scattering and nuclear reaction cross sections. The depth profiles of all constituents extracted from the simulation are compared for both methods.
Measurements of the deuterium particle flux and energy to the divertor of the DIII-D tokamak during a series of plasmas that terminated in disruptions have been made using a silicon collector probe installed on the DiMES (divertor materials exposure system) mechanism. During the steady state portion of each discharge, the probe was located in the private flux region, but immediately before disrupting the plasma, by injecting either Ar or D2 gas, the strike point of the outer divertor leg was positioned over the probe. Comparison of the amount of retained D in the probe for the two types of disruptions indicates that much of the trapped D could have resulted from exposure in the private flux zone prior to the disruption. Measurements of the depth distribution of the trapped D in the Si imply that the incident ion energy was approximately 100 eV at normal incidence and decreased slightly at oblique angles. The measurements give an upper bound to the energy of deuterons striking the divertor floor in the vicinity of the strikepoint during disruptions.
Thin metal films (∼ 100 nm thick) of Be, W, V and Mo, were deposited on a Si depth-marked graphite sample and exposed to the steady-state outer strike point on DIII-D in order to measure their respective erosion rates. Gross erosion rates and redeposition lengths are found to decrease with the atomic number of the metallic species, as expected. The maximum net erosion rate for carbon, which occurs near the separatrix, increased from 4 to 16 nm/s when the incident heat flux was increased from 0.7 to 2 MW/m2. Comparisons of the measured carbon erosion with REDEP code calculations show good agreement for both the absolute net erosion rate and its spatial variation. Visible spectroscopic measurements of singly ionized Be (BeII 4674 Å) have determined that the erosion process reaches steady-state during the exposure.
Lithium wall conditioning has been used in a recent campaign evaluating high performance negative central shear (NCS) discharges. During this campaign, the highest values of stored energy (4.4 MJ), neutron rate (2.4 x 10{sup 16}/s), and nT{sub i}{tau} (7 x 10{sup 20} m{sup -3}-keV-s) achieved to date in DIII-D were obtained. High performance NCS discharges were achieved prior to beginning lithium conditioning, but it is clear that shot reproducibility and performance were improved by lithium conditioning. Central and edge oxygen concentrations were reduced after lithium conditioning, Lithium conditioning, consisting of up to four pellets injected at the end of the preceding discharge, allowed the duration of the usual inter-shot helium glow discharge to be reduced and reproducible high auxiliary power discharges, P{sub NBI} {<=} 22 MW, were obtained with plasma currents up to 2.4 MA.