Pressure-induced phase transitions in energetic materials

Explosives and propellants, known generically as energetic materials, are widely used in applications that include mining, munitions, and automotive safety. Key properties of these materials include: reliable performance under a range of environmental conditions; long-term stability; environmental impact; processability; sensitivity to accidental initiation through stimuli such as impact, shock, friction, and electrostatic discharge. Many of these properties are affected by the crystal structure of the energetic material. Explosives experience elevated pressures and temperatures under detonation conditions - such conditions often induce phase transitions in the energetic material. Hence detailed studies of pressure-induced structural changes in these materials are essential in order to understand and model fully their behaviour. This presentation will describe some recent high-pressure studies (using a combination of X-ray and neutron diffraction techniques) on 2,4-dinitroanisole (DNAN), an insensitive explosive that is replacing TNT in some applications [1,2]. DNAN shows rich pressure-induced polymorphism, with at least four high-pressure forms having been identified to date. One of the structures provides insight into as to why DNAN is particularly insensitive to initiation by shock. The presentation will also describe the interplay between experiment and theory, which will be illustrated by experimental and computational high-pressure studies of 1,1-diamino-2,2-dinitroethene (DADNE or FOX-7). A very subtle phase transition has been identified at a pressure of ~2.0 GPa and the implications of this will be discussed in relation to the observed structural changes and properties of this material.

Single crystal diffraction at high energy and high pressure on I15 at DLS

The Extreme Condition beamline (I15) at the Diamond Light Source is a dedicated beamline for powder as well as single crystal diffraction on samples at extreme conditions in pressure or temperature. Single crystal data on either pressurized samples in a diamond anvil cell (DAC) or at ambient conditions are routinely done on a diffractometer scanning φ and ω using X-rays with energies in the range from 20 keV to 80 keV. Depending on the sample beam sizes varying from 20 μm to several 100 μm can be used. Data are recorded with an Atlas CCD (Agilent Technologies) and then treated with the Crysalis software package. In this contribution we highlight the very high accuracy of single-crystals data obtainable at I15 on two examples of single crystals in a DAC (E = 40 keV) and a sample at ambient conditions (E = 60 keV). A single crystal of the binary transition metal compound FeGe (B20 structure, space group P213, Z=4) was studied up to 11 GPa to determine the evolution of the inter-atomic distances (both atoms occupy the 4a Wyckoff positions). More than 200 unique data could be used to refine 7 parameters with an average R1 on all data of ~7%. Very high quality data have also been obtained for single crystals from the field of chemical crystallography, for which not only connectivity but also small bonding features can be detected. For example in l,6;8,13 biscarbonyl[14]annulene the progressive loss of aromatic character could be monitored and, in a special setup, the data allowed for the refinement of an unconstrained multipolar model. The use of 60 keV photons was crucial for an experiment on natural diamonds containing a variety of inclusions. At these energies the absorption of the diamond can be neglected. The aim of the study was to obtain information on possible recurrent crystallographic relationships between the inclusions and the diamond host on a significant number of extremely rare natural diamonds containing minerals.

Electron density of molecular crystals at high pressure from synchrotron data

Accurate electron density mapping is quite a common practice for crystals cooled at low temperature and accurately measured. This is not true for species under external perturbation, due to complicated experimental conditions. Studying molecular crystals in excited states is a challenge, Coppens(2009), and a purely experimental electron density mapping is not possible at present. So far, the same limitation affected molecular crystals at high pressure, with only few attempts to use theoretical multipoles to fit experimental data, Fabbiani (2011). Here we report on the first unconstrained multipolar model, refined for syn-l,6;8,13 biscarbonyl[14]annulene (BCA) at P=7.7 GPa. BCA was the subject of a low temperature data collection by Destro (1995). The molecule (close to C2v symmetry) has a fair aromaticity, but it progressively localizes double and single bonds as a function of pressure. At 7.7 GPa the geometrical distortion is quite evident and mirrored by the electron density. The experiment, carried out at Diamond Light Source, was possible combining: a) high energy (40 Kev) to overcome the resolution problems caused by diamond anvil cells and reduce absorption and extinction; b) microfocused beam (30 micron) to minimize spurious X-ray diffusion; c) two crystals in the DAC, to increase data coverage; d) sufficient pressure to quench atomic motion. The final agreement is obviously worse than what typically obtained at ambient pressure. However, the model is satisfactory because: a) the deformation density is sensible and in agreement with the calculated one; b) the distribution of residuals is normal and no significant error is evident. The study proves that aromatic molecules are more reactive when squeezed, in keeping with the recent theoretical study by Hoffmann et al. on benzene. The Figure shows the static deformation density of BCA in 3D, obtained from a multipolar model refined against the experimental structure factors.