Three novel anti-perovskite compounds, formulated as Cs3X[B12H12] (X- = [NO3]-, [ClO3]-, and [ClO4]-), were successfully synthesized through the direct mixing of aqueous solutions containing Cs2[B12H12] and CsX (X-: [NO3]-, [ClO3]-, [ClO4]-), followed by isothermal evaporation. All three compounds crystallize in the orthorhombic space group Pnma, exhibiting relatively similar unit-cell parameters (e.g., Cs3[ClO3][B12H12]: a = 841.25(5) pm, b = 1070.31(6) pm, c = 1776.84(9) pm). The crystal structures were determined using single-crystal X-ray diffraction, revealing a distorted hexagonal anti-perovskite order for each. Thermal analysis indicated that the placing oxidizing anions X- into the 3 Cs+ + [B12H12]2- blend leads to a reduction in the thermal stability of the resulting anti-perovskites Cs3X[B12H12] as compared to pure Cs2[B12H12], so thermal decomposition commences at lower temperatures, ranging from 320 to 440 °C. Remarkably, the examination of the energy release through DSC studies revealed that these compounds are capable of setting free a substantial amount of energy, up to 2000 J/g, upon their structural collapse under an inert-gas atmosphere (N2). These three compounds represent pioneering members of the first ever anti-perovskite high-energy compounds based on hydro-closo-borates.
Keywords: X-ray crystallography; anti-perovskite structure; high-energy materials; hydroborates.