Nanocrystal (NC)
self-assembly is a versatile platform for materials
engineering at the mesoscale. The NC shape anisotropy leads to structures
not observed with spherical NCs. This work presents a broad structural
diversity in multicomponent, long-range ordered superlattices (SLs)
comprising highly luminescent cubic CsPbBr
3
NCs (and FAPbBr
3
NCs) coassembled with the spherical, truncated cuboid, and
disk-shaped NC building blocks. CsPbBr
3
nanocubes combined
with Fe
3
O
4
or NaGdF
4
spheres and
truncated cuboid PbS NCs form binary SLs of six structure types with
high packing density; namely, AB
2
, quasi-ternary ABO
3
, and ABO
6
types as well as previously known NaCl,
AlB
2
, and CuAu types. In these structures, nanocubes preserve
orientational coherence. Combining nanocubes with large and thick
NaGdF
4
nanodisks results in the orthorhombic SL resembling
CaC
2
structure with pairs of CsPbBr
3
NCs on
one lattice site. Also, we implement two substrate-free methods of
SL formation. Oil-in-oil templated assembly results in the formation
of binary supraparticles. Self-assembly at the liquid–air interface
from the drying solution cast over the glyceryl triacetate as subphase
yields extended thin films of SLs. Collective electronic states arise
at low temperatures from the dense, periodic packing of NCs, observed
as sharp red-shifted bands at 6 K in the photoluminescence and absorption
spectra and persisting up to 200 K.