Host–guest
inclusion, constructed by inserting small molecules
into voids of energetic crystals, is a novel strategy for creating
new energetic materials (EMs) with desired energy and safety. To provide
an atomistic-level insight into the fact that small guest molecules
can effectively regulate the stability and sensitivity of CL-20, we
conducted ReaxFF-lg reactive molecular dynamics simulations on electric-field
(EF)-induced decomposition of two typical host–guest EMs, CL-20/H2O2 and CL-20/N2O, and compared it to
that of α-CL-20 and ε-CL-20. Our findings show that the
sensitivity order of the CL-20-based EMs under EFs, α-CL-20/H2O2 > ε-CL-20 > α-CL-20 > α-CL-20/N2O, agrees well with the sensitivity obtained from the experiment
(ε-CL-20 > α-CL-20 > α-CL-20/N2O). Different
effects of H2O2 and N2O molecules
were found responsible for the distinct stability and sensitivity
of these materials toward EFs. On the one hand, H2O2 accelerate(s) the structural transformation of CL-20 and
thus increases the sensitivity, because the wobbling NO2 group reduces the stability of CL-20 by weakening its adjacent C–N
bonds, whereas N2O makes this transition less likely, resulting
in low sensitivity of α-CL-20/N2O. On the other hand,
H2O2 and its decomposition intermediate OH radical
can promote destruction of CL-20’s cage structure and produce
a large amount of water molecules to release heat, making CL-20/H2O2 to decompose faster than ε-CL-20. N2O molecules rarely react with CL-20 molecules but absorb heat
from the surrounding decomposed CL-20 and thus slow down CL-20’s
decomposition, resulting in low sensitivity of α-CL-20/N2O, as confirmed by transition-state calculations. The results
provide a comprehensive understanding of the stability and sensitivity
of CL-20-based host–guest explosives under EFs.