Structure, Bonding, and Vibrational Dynamics of a Triamine High Energy Density Material under Pressure

• Published in: Journal of physical chemistry. C 2024-09, Vol.128 (38), p.16110-16119
• Main Authors: Whipple, Zachary L., Ripani, Roma R., Brahmbhatt, Janki, Ahart, Muhtar, Salke, Nilesh P., Meng, Yue, Liu, Zhenxian, Chariton, Stella, Gramsch, Stephen A., Chaudhuri, Santanu, Parisi, Emmanuele, Centore, Roberto, Hemley, Russell J.
• Format: Article
• Language: English
• Subjects: C: Physical Properties of Materials and Interfaces; Compression; Diffraction; Layers; Materials; Molecular interactions
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/acs.jpcc.4c03637

High energy density materials have complex intermolecular interactions which influence their stability and performance. We used a combination of synchrotron X-ray diffraction, synchrotron infrared spectroscopy, and Raman vibrational spectroscopy, supplemented by density functional theory calculations, to probe pressure-induced changes in structure and intermolecular interactions of 1H,4′H-[3,3′-bis­(1,2,4-triazole)]-4′,5,5′-triamine as a model high energy density material up to 40 GPa. We find that compression of the triamine is accompanied by increased intermolecular interactions that give rise to an interesting evolution of the structure and bonding with pressure. Analysis of the equation of state determined from the X-ray diffraction indicates a change in compression mechanism near 19 GPa consistent with changes in vibrational spectra that provide evidence for a structural rearrangement associated with changes in hydrogen bonding near that pressure. The overall compressional behavior calculated theoretically agrees with that observed experimentally though differences are found that indicate the need for improved treatment of the intermolecular interactions including hydrogen bonding under pressure.