The separation of ammonia from H2/N2/NH3 mixtures is an important step in ammonia decomposition
for
hydrogen production and ammonia synthesis from H2 and N2 based nonaqueous technologies. Metal–organic frameworks
(MOFs) are considered as potential materials for capturing ammonia.
In the present work, high-throughput screening of 2932 Computation-Ready
Experimental MOFs (CoRE MOFs) was carried out for ammonia capture
from H2/N2/NH3 mixtures by Grand
Canonical Monte Carlo (GCMC) simulations. It was found that the high-performing
MOFs are characterized by tube-like channels, moderate LCD (largest
cavity diameter) (4–7.5 Å), and high Q
st
0(NH3) (the isosteric heat of NH3 adsorption)
(>45 kJ/mol). MOFs with high NH3 adsorption capacity
often
feature moderate surface area, while the surface area of MOFs with
high NH3 selectivity is relatively lower, which limits
the NH3 adsorption capacity. Q
st
0 and the Henry’s constant (K
H
) are two energy descriptors describing the interactions
between adsorbents and adsorbates. The former has a stronger correlation
with the adsorption selectivity, while the latter has a stronger correlation
with the adsorption capacity. By analyzing the molecular density distribution
of adsorbates in high-performing MOFs, it was found that unsaturated
coordinated metal sites provide the main functional binding sites
for NH3. Most MOFs with high NH3 selectivity
have multiple different metal nodes or other atoms except C, O, and
H, such as N and P. Multiple metal nodes and nonmetallic atoms provide
more functional binding sites. Finally, the adsorption behavior with
various concentrations of gas mixtures was examined to verify the
universality of the screening calculations, and the effect of framework
flexibility on adsorption performance was explored.