Metal–organic frameworks (MOFs)crystalline
coordination
polymerswith unique characteristics such as structural designability
accompanied by tunable electronic properties and intrinsic uniform
nanopores have become the platform for applications in diverse scientific
areas ranging from nanotechnology to energy/environmental sciences.
To utilize the superior features of MOF in potential applications,
the fabrication and integration of thin films are of importance and
have been actively sought. Especially, downsized MOFs into nanosheets
can act as ultimately thin functional components in nanodevices and
potentially display unique chemical/physical properties rarely seen
in bulk MOFs. Assembling nanosheets by aligning amphiphilic molecules
at the air/liquid interface has been known as the Langmuir technique.
By utilizing the air/liquid interface as a reaction field between
metal ions and organic ligands, MOFs are readily formed into the nanosheet
state. The expected features in MOF nanosheets including electrical
conduction largely depend on the nanosheet characteristics such as
lateral size, thickness, morphology, crystallinity, and orientation.
However, their control has not been achieved as yet. Here, we demonstrate
how changing the concentration of a ligand spread solution can modify
the assembly of MOF nanosheets, composed of 2,3,6,7,10,11-hexaiminotriphenylene
(HITP) and Ni2+ ions (HITP-Ni-NS), at the
air/liquid interface. A systematic increase in the concentration of
the ligand spread solution leads to the enlargement of both the lateral
size and the thickness of the nanosheets while retaining their perfect
alignment and preferred orientation. On the other hand, at much higher
concentrations, we find that unreacted ligand molecules are included
in HITP-Ni-NS, introducing disorder in HITP-Ni-NS. These findings can develop further sophisticated control of MOF
nanosheet features, accelerating fundamental and applied studies on
MOFs.