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All sourcesNASA NTRSDOE OSTI
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. IX. LiCoO 2

X-ray photoelectron spectroscopy (XPS) and x-ray-induced Auger electron spectroscopy were used to analyze untreated LiCoO 2 powder obtained from BTR New Energy Materials, Inc. X-ray photoelectron and x-ray-induced Auger electron spectra were obtained using incident monochromatic Al Kα radiation at 0.834 01 nm. A survey spectrum together with Co 2p, O 1s, C 1s, Co 3s, Co 3p, and Li 1s are presented. The spectra indicate the principal core level photoelectron and Auger electron signals and show only minor tin contamination. Making use of the O 1s, Co 3p, and Li 1s lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surface of LiCo 0.9 O 1.7 .

25 ENERGY STORAGE↗
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. VI. LiNi 0.4 Co 0.2 Mn 0.4 O 2

X-ray photoelectron spectroscopy (XPS) was used to analyze fresh LiNi 0.4 Co 0.2 Mn 0.4 O 2 powder obtained from TODA America. XP spectra were obtained using incident monochromatic Al Kα radiation at 0.834 01 nm. A survey spectrum together with Ni 2p, Co 2p, Mn 2p, Ni LMM, O 1s, C 1s, Al 2s, Ni 3s, Co 3s, Mn 3s, Ni 3p, Co 3p, Li 1s, and Mn 3p are presented. The spectra indicate the principal core level photoelectron and Auger electron. Making use of the O 1s, Ni 3p, Co 3p, Mn 3p, Li 1s lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surface of LiNi 0.5 Co 0.2 Mn 0.5 O 1.9 .

25 ENERGY STORAGE↗
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. VII. LiNi 0.33 Co 0.33 Mn 0.33 O 2

X-ray photoelectron spectroscopy (XPS) was used to analyze fresh LiNi 0.33 Co 0.33 Mn 0.33 O 2 powder obtained from TODA America. XP spectra were obtained using incident monochromatic Al Kα radiation at 0.834 01 nm. A survey spectrum together with Ni 2p, Co 2p, Mn 2p, Ni LMM, O 1s, C 1s, Al 2s, Ni 3s, Co 3s, Mn 3s, Ni 3p, Co 3p, Li 1s, and Mn 3p are presented. The spectra indicate the principal core level photoelectron and Auger electron signals. Making use of the O 1s, Ni 3p, Co 3p, Mn 3p, Li 1s lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surface of LiNi 0.4 Co 0.1 Mn 0.7 O 2.0 .

25 ENERGY STORAGE↗
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. III. LiNi 0.6 Co 0.2 Mn 0.2 O 2

X-ray photoelectron spectroscopy (XPS) was used to analyze fresh LiNi 0.6 Co 0.2 Mn 0.2 O 2 powder obtained from Ecopro Company, Ltd.. XP spectra were obtained using incident monochromatic Al Kα radiation at 0.834 01 nm. A survey spectrum together with Ni 2p, Co 2p, Mn 2p, Ni LMM, O 1s, C 1s, Al 2s, Ni 3s, Co 3s, Mn 3s, Ni 3p, Co 3p, Li 1s, and Mn 3p are presented. The spectra indicate the principal core level photoelectron and Auger electron. Making use of the O 1s, Ni 3p, Co 3p, Mn 3p, Li 1s lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surface of LiNi 0.2 Co 0.05 Mn 0.1 O 0.7 .

25 ENERGY STORAGE↗
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. I. LiNi 0.8 Co 0.15 0.05 O 2

X-ray photoelectron spectroscopy (XPS) was used to analyze fresh LiNi 0.8 Co 0.1 5Al 0.05 O 2 powder obtained from TODA America. XP spectra were obtained using incident monochromatic Al Kα radiation at 0.834 01 nm. A survey spectrum together with Ni 2p, Co 2p, Ni LMM, O 1s, C 1s, Al 2s, Ni 3s, Co 3s, Al 2p, Ni 3p, Co 3p, and Li 1s are presented. The spectra indicate the principal core level photoelectron and Auger electron signals and show carbon with only minor sulfur contamination. Making use of the O 1s, Al 2s, Ni 3p, Co 3p, Li 1s lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surface of LiNi 0.2 Co 0.03 Al 0.1 O 0.7 .

25 ENERGY STORAGE↗
DOE OSTI2025

Solving the Pulsed-Power Driven Inertial Fusion Energy Standoff Problem (Abbreviated Final Report)

The standoff problem in pulsed-power driven IFE (Inertial Fusion Energy) refers to the problem of electrically connecting a fusion target with the driver in a way that preserves the driver/target interface in the presence of a large fusion energy release (100’s of megajoules to 1000 megajoules). High yield fusion drivers for stockpile stewardship applications have similar concerns, but without the complication of the high repetition rate needed for energy production. All proposed IFE or high yield systems have the challenge of protecting the reactor vessel and driver from the energy release, but pulsed power drivers have the additional challenge of establishing an electrical connection in a way that does not create excessive debris or require costly/massive structures that must be expendable. Fortunately, there are conceptual solutions in the form of very low mass transmission lines, usually in the form of wires or foils, since very little mass is needed to overcome the magnetic forces driving the transmission lines apart or provide a low resistance pathway given the short pulse duration of the driver. Several important aspects of the standoff problem were analyzed in the course of this LDRD project. Conceptual means of introducing the low mass transmission lines into the reactor chamber were proposed, including analysis of methods to retain the power flow gap between the electrodes in the presence of the chamber environment. The energy losses due to ohmic dissipation and magnetic acceleration of the low mass transmission lines were evaluated for candidate driver pulses and different transmission line masses, and the fluence of x-ray and neutron energy on the persistent power flow structures that must survive the pulse of energy were evaluated. Finally, means of rapidly pumping down the chamber were explored as a way to return the system to low pressure following the multi-atmosphere post-pulse pressure rise. The overall conclusion from the analysis is that, while the reactor environment creates stressful conditions for a low mass transmission line standoff system, there are concepts expending 10 kg or less of electrode mass each pulse with the potential to mitigate the stresses and successfully drive fusion targets. Whether such a system could lead to a practical and economical fusion reactor would require extensive research and development beyond the scope of the feasibility study.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗
NASA NTRS2001

Hippocampal place-cell firing during movement in three-dimensional space

"Place" cells of the rat hippocampus are coupled to "head direction" cells of the thalamus and limbic cortex. Head direction cells are sensitive to head direction in the horizontal plane only, which leads to the question of whether place cells similarly encode locations in the horizontal plane only, ignoring the z axis, or whether they encode locations in three dimensions. This question was addressed by recording from ensembles of CA1 pyramidal cells while rats traversed a rectangular track that could be tilted and rotated to different three-dimensional orientations. Cells were analyzed to determine whether their firing was bound to the external, three-dimensional cues of the environment, to the two-dimensional rectangular surface, or to some combination of these cues. Tilting the track 45 degrees generally provoked a partial remapping of the rectangular surface in that some cells maintained their place fields, whereas other cells either gained new place fields, lost existing fields, or changed their firing locations arbitrarily. When the tilted track was rotated relative to the distal landmarks, most place fields remapped, but a number of cells maintained the same place field relative to the x-y coordinate frame of the laboratory, ignoring the z axis. No more cells were bound to the local reference frame of the recording apparatus than would be predicted by chance. The partial remapping demonstrated that the place cell system was sensitive to the three-dimensional manipulations of the recording apparatus. Nonetheless the results were not consistent with an explicit three-dimensional tuning of individual hippocampal neurons nor were they consistent with a model in which different sets of cells are tightly coupled to different sets of environmental cues. The results are most consistent with the statement that hippocampal neurons can change their "tuning functions" in arbitrary ways when features of the sensory input or behavioral context are altered. Understanding the rules that govern the remapping phenomenon holds promise for deciphering the neural circuitry underlying hippocampal function.

Non-NASA Center↗
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. II. LiNi 0.8 Co 0.1 Mn 0.1 O 2

X-ray photoelectron spectroscopy (XPS) was used to analyze fresh LiNi 0.8 Co 0.1 Mn 0.1 O 2 powder obtained from Targray Technology International, Inc.. XP spectra were obtained using incident monochromatic Al Kα radiation at 0.834 01 nm. A survey spectrum together with Ni 2p, Co 2p, Mn 2p, Ni LMM, O 1s, C 1s, Al 2s, Ni 3s, Co 3s, Mn 3s, Ni 3p, Co 3p, Li 1s, and Mn 3p are presented. The spectra indicate the principal core level photoelectron and Auger electron signals and show only minor sulfur contamination. Making use of the O 1s, Ni 3p, Co 3p, Mn 3p, Li 1s lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surface of LiNi 0.4 Co 0.02 Mn 0.1 O 0.8 .

25 ENERGY STORAGE↗
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. V. LiNi 0.4 Co 0.3 0.3 O 2

X-ray photoelectron spectroscopy (XPS) and x-ray-induced Auger electron spectroscopy were used to analyze untreated LiNi 0.4 Co 0.3 Mn 0.3 O 2 powder obtained from TODA America. X-ray photoelectron and x-ray-induced Auger electron spectra were obtained using incident monochromatic Al Kα radiation at 0.834 01 nm. A survey spectrum together with Ni 2p, Co 2p, Mn 2p, Ni LMM, O 1s, C 1s, Ni 3s, Co 3s, Mn 3s, Ni 3p, Co 3p, Li 1s, and Mn 3p are presented. The spectra indicate the principal core level photoelectron and Auger electron signals. Making use of the O 1s, Ni 3p, Co 3p, Mn 3p, and Li 1s lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surface of LiN i0.4 Co 0.2 Mn 0.3 O 1.6 .

25 ENERGY STORAGE↗
NASA NTRS2007

NASA Tech Briefs, October 2007

Topics covered include; Wirelessly Interrogated Position or Displacement Sensors; Ka-Band Radar Terminal Descent Sensor; Metal/Metal Oxide Differential Electrode pH Sensors; Improved Sensing Coils for SQUIDs; Inductive Linear-Position Sensor/Limit-Sensor Units; Hilbert-Curve Fractal Antenna With Radiation- Pattern Diversity; Single-Camera Panoramic-Imaging Systems; Interface Electronic Circuitry for an Electronic Tongue; Inexpensive Clock for Displaying Planetary or Sidereal Time; Efficient Switching Arrangement for (N + 1)/N Redundancy; Lightweight Reflectarray Antenna for 7.115 and 32 GHz; Opto-Electronic Oscillator Using Suppressed Phase Modulation; Alternative Controller for a Fiber-Optic Switch; Strong, Lightweight, Porous Materials; Nanowicks; Lightweight Thermal Protection System for Atmospheric Entry; Rapid and Quiet Drill; Hydrogen Peroxide Concentrator; MMIC Amplifiers for 90 to 130 GHz; Robot Would Climb Steep Terrain; Measuring Dynamic Transfer Functions of Cavitating Pumps; Advanced Resistive Exercise Device; Rapid Engineering of Three-Dimensional, Multicellular Tissues With Polymeric Scaffolds; Resonant Tunneling Spin Pump; Enhancing Spin Filters by Use of Bulk Inversion Asymmetry; Optical Magnetometer Incorporating Photonic Crystals; WGM-Resonator/Tapered-Waveguide White-Light Sensor Optics; Raman-Suppressing Coupling for Optical Parametric Oscillator; CO2-Reduction Primary Cell for Use on Venus; Cold Atom Source Containing Multiple Magneto- Optical Traps; POD Model Reconstruction for Gray-Box Fault Detection; System for Estimating Horizontal Velocity During Descent; Software Framework for Peer Data-Management Services; Autogen Version 2.0; Tracking-Data-Conversion Tool; NASA Enterprise Visual Analysis; Advanced Reference Counting Pointers for Better Performance; C Namelist Facility; and Efficient Mosaicking of Spitzer Space Telescope Images.

Source record↗
DOE OSTI2022

Ultra‐Thin Single‐Particle‐Layer Sodium Beta‐Alumina‐Based Composite Polymer Electrolyte Membrane for Sodium‐Metal Batteries

Inorganic/organic composite polymer electrolytes (CPEs) with good flexibility and electrode contact have been pursued for solid-state sodium-metal batteries. However, the application of CPEs for high energy density solid-state sodium-metal batteries is still limited by the low Na + conductivity, large thickness, and low ion transference number. Herein, an ultra-thin single-particle-layer (UTSPL) composite polymer electrolyte membrane with a thickness of ≈20 µm straddled by a sodium beta-alumina ceramic electrolyte (SBACE) is presented. A ceramic Na + -ion electrolyte that bridges or percolates across an ultra-thin and flexible polymer membrane provides: 1) the strength and flexibility from the polymer membrane, 2) excellent electrolyte/electrode interfacial contact, and 3) a percolation path for Na + -ion transfer. Owing to this novel design, the obtained UTSPL-35SBACE membrane exhibits a high Na+-ion conductivity of 0.19 mS cm -1 and a transference number of 0.91 at room temperature, contributing to long-term cycling stability of symmetric sodium cells with a small overpotential. The assembled quasi-solid-state cell with the as-prepared UTSPL-35SBACE membrane displays superior cycling performance with a discharge capacity of 105 mAh g -1 at 0.5 °C rate after 100 cycles and excellent rate performance (82 mAh g -1 at 5 °C rate) at room temperature with the potassium manganese hexacyanoferrate (KMHCF)@CNTs/CNFs cathode, where KMHCF refers to potassium manganese hexacyanoferrate.

25 ENERGY STORAGE↗
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. X. Li 4 Ti 5 O 12

X-ray photoelectron spectroscopy (XPS) and x-ray-induced Auger electron spectroscopy were used to analyze untreated Li 4 Ti 5 O 12 powders obtained from Ishihara Sangyo Kaisha, Ltd. and Samsung Fine Chemicals Company, Ltd. X-ray photoelectron and x-ray-induced Auger electron spectra were obtained using incident monochromatic Al Kα radiation at 0.834 01 nm. A survey spectrum together with O 1s, Ti 2p, C 1s, Ti 3s, Li 1s, and Ti 3p are presented. The spectra indicate the principal core level photoelectron and Auger electron signals and show only minor potassium signal. Making use of the O 1s, Li 1s, and Ti 3p lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surfaces from Ishihara Sangyo Kaisha, Ltd. and Samsung Fine Chemicals Company, Ltd. of Li 4 Ti 4.7 O 14.1 and Li 4 Ti 4.3 O 13.2 , respectively.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2020

Thin Cation-Exchange Layers Enable High-Current-Density Bipolar Membrane Electrolyzers via Improved Water Transport

With suitable water dissociation (WD) catalysts, bipolar membranes (BPMs) can efficiently dissociate water into H + and OH – at the junction between anion- and cation-exchange layers (AEL and CEL, respectively). First, however, water must be transported through the AEL or CEL and thus against the outward flow of hydrated H + and OH – . This is a challenge intrinsic to the BPM architecture and limits operation to current densities typically less than ~0.5 A·cm –2 . Here we explore how water transport affects durability and performance in reference alkaline and acidic membrane electrolyzers, and we use the insight gained to design BPMs with improved water transport. We demonstrate a thin-CEL BPM (2-μm Nafion CEL|~200 nm TiO 2 |~200 nm NiO + ionomer|50 μm Sustainion AEL) which maintains a pH difference of ~14 units between the anode and cathode for current densities of up to 3.4 A·cm –2 with a total water electrolysis voltage of ~4 V and an estimated WD overpotential of ~1.5 V. Finally, such high-current-density operation is crucial for key emerging BPM applications, including in water and carbon-dioxide electrolyzers and in (regenerative) fuel cells.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2019

Lithium-based transition-metal oxides for battery electrodes analyzed by x-ray photoelectron spectroscopy. VIII. Li 1.2 Ni 0.15 Co 0.1 Mn 0.55 O 2

X-ray photoelectron spectroscopy (XPS) and x-ray-induced Auger electron spectroscopy were used to analyze untreated Li 1.2 Ni 0.15 Co 0.1 Mn 0.55 O 2 powder obtained from TODA America. X-ray photoelectron and x-ray-induced Auger electron spectra were obtained using incident monochromatic Al Kα radiation at 0.83 01 nm. A survey spectrum together with Ni 2p, Co 2p, Mn 2p, Ni LMM, O 1s, C 1s, Ni 3s, Co 3s, Mn 3s, Ni 3p, Co 3p, Li 1s, and Mn 3p are presented. The spectra indicate the principal core level photoelectron and Auger electron signals. Making use of the O 1s, Ni 3p, Co 3p, Mn 3p, and Li 1s lines and neglecting the components related to surface contaminants, XPS quantitative analysis reveals an altered stoichiometry of the air-exposed powder surface of Li 1.2 Ni 0.4 Co 0.2 Mn 0.9 O 2.8 .

32 ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATI↗
DOE OSTI2020

Macroscale and Nanoscale Photoelectrochemical Behavior of p-Type Si(111) Covered by a Single Layer of Graphene or Hexagonal Boron Nitride

Two-dimensional (2D) materials may enable a general approach to the introduction of a dipole at a semiconductor surface as well as control over other properties of the double layer at a semiconductor/liquid interface. Vastly different properties can be found in the 2D materials currently studied due in part to the range of the distribution of density-of-states. In this work, the open-circuit voltage (V oc ) of p-Si–H, p-Si/Gr (graphene), and p-Si/h-BN (hexagonal boron nitride) in contact with a series of one-electron outer-sphere redox couples was investigated by macroscale measurements as well as by scanning electrochemical cell microscopy (SECCM). The band gaps of Gr and h-BN (0–5.97 eV) encompass the wide range of band gaps for 2D materials, so these interfaces (p-Si/Gr and p-Si/h-BN) serve as useful references to understand the behavior of 2D materials more generally. The value of Voc shifted with respect to the effective potential of the contacting solution, with slopes (ΔV oc /ΔE Eff ) of -0.27 and -0.38 for p-Si/Gr and p-Si/h-BN, respectively, indicating that band bending at the p-Si/h-BN and p-Si/Gr interfaces responds at least partially to changes in the electrochemical potential of the contacting liquid electrolyte. Additionally, SECCM is shown to be an effective method to interrogate the nanoscale photoelectrochemical behavior of an interface, showing little spatial variance over scales exceeding the grain size of the CVD-grown 2D materials in this work. The measurements demonstrated that the polycrystalline nature of the 2D materials had little effect on the results and confirmed that the macroscale measurements reflected the junction behavior at the nanoscale.

2D material↗
DOE OSTI2017

2D metal carbides and nitrides (MXenes) for energy storage

The family of 2D transition metal carbides, carbonitrides and nitrides (collectively referred to as MXenes) has expanded rapidly since the discovery of Ti 3 C 2 in 2011. The materials reported so far always have surface terminations, such as hydroxyl, oxygen or fluorine, which impart hydrophilicity to their surfaces. About 20 different MXenes have been synthesized, and the structures and properties of dozens more have been theoretically predicted. Furthermore, the availability of solid solutions, the control of surface terminations and a recent discovery of multi-transition-metal layered MXenes offer the potential for synthesis of many new structures. The versatile chemistry of MXenes allows the tuning of properties for applications including energy storage, electromagnetic interference shielding, reinforcement for composites, water purification, gas- and biosensors, lubrication, and photo-, electro- and chemical catalysis. Attractive electronic, optical, plasmonic and thermoelectric properties have also been shown. Here, we present the synthesis, structure and properties of MXenes, as well as their energy storage and related applications, and an outlook for future research.

25 ENERGY STORAGE↗
DOE OSTI2020

Mathematical Modeling of Hydroxide-Exchange-Membrane Water Electrolyzer

Water electrolyzers can transform intermittent renewable energy like solar energy and wind energy into the chemical energy of hydrogen with zero greenhouse-gas emissions. The hydroxide-exchange membrane electrolyzer (HEME) combines the capability to produce pressurized hydrogen with the advantage of being able to use low or non-platinum group metal (PGM) electrocatalysts in the alkaline environment.1 Hydroxide salts, for example, KOH, are added to the HEME water feed on both anode and cathode to improve its performance. However, the specific mechanism of performance improvement still needs to be further understood. In addition, at high current densities, bubble evolution can result in mass-transport limitations, a less well studied phenomena. Mathematical modeling is ideal to explore these issues as it is cost and time efficient and can deconvolute the physics, processes, and observed phenomena and study the applied-voltage breakdown. In this work, we extend our previously developed 1D two-phase continuum model2 to study the varies processes in the HEME and provide insights on performance optimizations. First, the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) kinetics at different hydroxide concentrations have been studied by rotating disk electrodes (RDE) and implemented in the model. Then, the model is calibrated and validated against experimental HEME polarization curves for different KOH concentrations as a liquid electrolyte. The model clearly shows a performance increase with increasing KOH concentrations, which is consistent with the experimental results. The reduced ohmic resistance and increased electrochemical active surface area (ECSA) are the two main reasons for performance increase. The large amount of hydroxide in the liquid electrolyte not only helps to distribute the reactant hydroxide throughout the catalyst layer (CL), which reduces ohmic loss, but also enables reaction at the interface between the liquid electrolyte and electrocatalyst, which increases the ECSA. Applied-voltage breakdown demonstrates that the electrolyzer performance is dominated by anode kinetics and ohmic loss. A comparison with the DI water feed shows a more uniform current distribution in the anode CL when KOH is added, which indicates a higher utilization of the CL. Second, we present modeling on the effects of bubble coverage. As gas evolves, part of the ECSA is minimized due to bubble coverage. To account for this effect, an empirical relationship between the fractional bubble coverage and the current density is implemented in the model.3 The model shows this bubble coverage effect is more pronounced at large current densities with DI water feed. Acknowledgements This work was funded under the HydroGEN Consortium by the Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office, of the U. S. Department of Energy under contract number DE-AC02-05CH11231. References R. Abbasi, B. P. Setzler, S. Lin, J. Wang, Y. Zhao, H. Xu, B. Pivovar, B. Tian, X. Chen, G. Wu and Y. Yan, 31, 1805876 (2019). L. N. Stanislaw, M. R. Gerhardt and A. Z. Weber, ECS Transactions, 92, 767 (2019). H. Vogt and R. J. Balzer, Electrochimica Acta, 50, 2073 (2005).

Liu, Jiangjin↗
DOE OSTI2015

Investigation of the initial and volume recombination losses in gamma versatile cylindrical ionization chamber VGIC developed for gamma ray dosimetry

A versatile Gamma ionization chambers are used for flow control in systems with gamma nuclear reactors and reprocessing plants in and monitoring atmosphere around these facilities, this in order to protect staff. In the Laboratory Detection and Measures (LDM) Division for Study and Development of Nuclear Instrumentation (DSDNI) of CRNB, we designed, developed and characterized a versatile gamma ionization chamber (VGIC) to study experimentally its characteristics according to the geometry of the electrodes, the volume and pressure of the filler gas for the design of a gamma sealed chamber. The tests were conducted under the IEC (International Electro-technical Commission). In this paper, we present the results obtained in the various nuclear tests for characterization and calibration that we have made on the ionization chamber gamma VGIC prototype developed at our Department. To do this, three irradiators were operated at the Laboratory Calibration (SSDL) of the Department of Medical Physics Nuclear Research Center of Algiers (CRNA). Irradiator intensive gamma ({sup 60}Co: 1.25 MeV), one medium intensity gamma ({sup 137}Cs: 0.662 MeV) and 3rd low intensity ({sup 60}Co). Saturation curves and linearity were identified and the operating range and the sensitivity of the chamber have been deducted. The (I,V) characteristics of the chamber filled, with argon gas at 3 bar (0.3 M pa) pressure, for gamma ray irradiator sources were studied. To do so, the chamber was irradiated with gamma rays using different numbers of gamma sources (i.e. Up to 5). The plateau region is reached above 200 V and the detector operating voltage is found to be 600 V. It is observed that in the plateau region the slope is constant with an increase in the exposure rate. The (1/I, 1/V) and (I, l/V{sup 2}) characteristic curves reveal the presence of the initial and volume recombination losses. The volume recombination losses are found to be smaller than the initial recombination losses. Finally, in order to strengthen our results, we performed in the same conditions, a comparative characterization with another ionization gamma chamber type reference LND 504 (USA). (authors)

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗