
Understanding how polyhedra pack into extended arrangements is integral  to the design and discovery of crystalline materials at all length  scales
1, 2, 3. Much progress has been made in enumerating and characterizing the packing of polyhedral shapes
4, 5, 6, and the self-assembly of polyhedral nanocrystals into ordered superstructures
7, 8, 9.  However, directing the self-assembly of polyhedral nanocrystals into  densest packings requires precise control of particle shape
10, polydispersity
11, interactions and driving forces 
12.  Here we show with experiment and computer simulation that a range of  nanoscale Ag polyhedra can self-assemble into their conjectured densest  packings
6.  When passivated with adsorbing polymer, the polyhedra behave as  quasi-hard particles and assemble into millimetre-sized  three-dimensional supercrystals by sedimentation. We also show, by  inducing depletion attraction through excess polymer in solution, that  octahedra form an exotic superstructure with complex helical motifs  rather than the densest Minkowski lattice
13. Such large-scale 
Ag supercrystals may facilitate the design of scalable three-dimensional plasmonic metamaterials for sensing
14, 15, nanophotonics
16 and photocatalysis
17.
 
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