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Register a new userThermomechanical response of thickly tamped targets and diamond anvil cells under pulsed hard x-ray irradiation
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Added by
R. Stewart McWilliams
Publication date
2018
fields
Physics
and research's language is
English
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In the laboratory study of extreme conditions of temperature and density, the exposure of matter to high intensity radiation sources has been of central importance. Here we interrogate the performance of multi-layered targets in experiments involving high intensity, hard x-ray irradiation, motivated by the advent of extremely high brightness hard x-ray sources, such as free electron lasers and 4th-generation synchrotron facilities. Intense hard x-ray beams can deliver significant energy in targets having thick x-ray transparent layers (tampers) around samples of interest, for the study of novel states of matter and materials dynamics. Heated-state lifetimes in such targets can approach the microsecond level, regardless of radiation pulse duration, enabling the exploration of conditions of local thermal and thermodynamic equilibrium at extreme temperature in solid density matter. The thermal and mechanical response of such thick layered targets following x-ray heating, including hydrodynamic relaxation and heat flow on picosecond to millisecond timescales, is modelled using radiation hydrocode simulation, finite element analysis, and thermodynamic calculations. Assessing the potential for target survival over one or more exposures, and resistance to damage arising from heating and resulting mechanical stresses, this study doubles as an investigation into the performance of diamond-anvil high pressure cells under high x-ray fluences. Long used in conjunction with synchrotron x-ray radiation and high power optical lasers, the strong confinement afforded by such cells suggests novel applications at emerging high intensity x-ray facilities and new routes to studying thermodynamic equilibrium states of warm, very dense matter.
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Pressure calibration for most diamond-anvil cell (DAC) experiments is mainly based on the ruby scale, which is key to implement this powerful tool for high-pressure study. However, the ruby scale can often hardly be used for programmably-controlled DAC devices, especially the piezoelectric-driving cells, where a continuous pressure calibration is required. In this work, we present an effective pressure gauge for DACs made of manganin metal, based on the four-probe resistivity measurements. Pressure dependence of its resistivity is well established and shows excellent linear relations in the 0 - 30 GPa pressure range with a slope of 23.4 (9) GPa for the first-cycle compression, in contrast to that of multiple-cycle compression and decompression having a nearly identical slope of 33.7 (4) GPa likely due to the strain effect. In addition, such-established manganin scale can be used for continuously monitoring the cell pressure of piezoelectric-driving DACs, and the reliability of this method is also verified by the fixed-point method with a Bi pressure standard. Realization of continuous pressure calibration for programmably-controlled DACs would offer many opportunities for study of dynamics, kinetics, and critical behaviors of pressure-induced phase transitions.
Important discoveries have frequently been made through the studies of matter under high pressure. The conditions of the pressure environment are important for the interpretation of the experimental results. Due to various restrictions inside the pressure cell, detailed information relevant to the pressure environment, such as the pressure distribution, can be hard to obtain experimentally. Here we present the study of pressure distributions inside the pressure medium under different experimental conditions with NV centers in diamond particles as the sensor. These studies not only show a good spatial resolution, wide temperature and pressure working ranges, compatibility of the existing pressure cell design with the new method, but also demonstrate the usefulness to measure with these sensors as the pressure distribution is sensitive to various factors. The method and the results will benefit many disciplines such as material research and phase transitions in fluid dynamics.
Part I shows that quantitative measurements of heat capacity are theoretically possible inside diamond anvil cells via high-frequency Joule heating (100 kHz to 10 MHz), opening up the possibility of new methods to detect and characterize transformations at high-pressure such as the glass transitions, melting, magnetic orderings, or the onset of superconductivity. Here we test the possibility outlined in Part I, using prototypes and detailed numerical models. First, a coupled electrical-thermal numerical model shows that specific heat of metals inside diamond cells can be measured directly using $sim 1$ MHz frequency, with $< 10%$ accuracy. Second, we test physical models of high-pressure experiments, i.e. diamond-cell mock-ups. Metal foils of 2 to 6 $mu$m-thickness are clamped between glass insulation inside diamond anvil cells. Fitting data from 10 Hz to $sim 30$ kHz, we infer the specific heat capacities of Fe, Pt and Ni with $pm 20$ to $30%$ accuracy. The electrical test equipment generates -80 dBc spurious harmonics which overwhelm the thermally-induced harmonics at higher frequencies, disallowing the high precision expected from numerical models. An alternative Joule-heating calorimetry experiment, on the other hand, does allow absolute measurements with $< 10%$ accuracy, despite the -80 dBc spurious harmonics: the measurement of thermal effusivity, $sqrt{rho c k}$ ($rho$, $c$ and $k$ being density, specific heat and thermal conductivity), of the insulation surrounding a thin-film heater. Using a $sim 50$ nm-thick Pt heater surrounded by glass and 10 Hz to 300 kHz frequency, we measure thermal effusivity with $pm 6%$ accuracy inside the sample chamber of a diamond anvil cell.
Intense, pulsed ion beams locally heat materials and deliver dense electronic excitations that can induce materials modifications and phase transitions. Materials properties can potentially be stabilized by rapid quenching. Pulsed ion beams with (sub-) ns pulse lengths have recently become available for materials processing. Here, we optimize mask geometries for local modification of materials by intense ion pulses. The goal is to rapidly excite targets volumetrically to the point where a phase transition or local lattice reconstruction is induced followed by rapid cooling that stabilizes desired materials properties fast enough before the target is altered or damaged by e. g. hydrodynamic expansion. We performed HYDRA simulations that calculate peak temperatures for a series of excitation conditions and cooling rates of silicon targets with micro-structured masks and compare these to a simple analytical model. The model gives scaling laws that can guide the design of targets over a wide range of pulsed ion beam parameters.
Understanding nano- and micro-scale crystal strain in CVD diamond is crucial to the advancement of diamond quantum technologies. In particular, the presence of such strain and its characterization present a challenge to diamond-based quantum sensing and information applications -- as well as for future dark matter detectors where directional information of incoming particles is encoded in crystal strain. Here, we exploit nanofocused scanning X-ray diffraction microscopy to quantitatively measure crystal deformation from growth defects in CVD diamond with high spatial and strain resolution. Combining information from multiple Bragg angles allows stereoscopic three-dimensional reconstruction of strained volumes; the diffraction results are validated via comparison to optical measurements of the strain tensor based on spin-state-dependent spectroscopy of ensembles of nitrogen vacancy (NV) centers in the diamond. Our results open a path towards directional detection of dark matter via X-ray measurement of crystal strain, and provide a new tool for diamond growth analysis and improvement of defect-based sensing.
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