Large crystalline molecular shells, such as some viruses and fullerenes, buckle spontaneously into icosahedra. Meanwhile multicomponent microscopic shells buckle into various polyhedra, as observed in many organelles. Although elastic theory explains one-component icosahedral faceting, the possibility of buckling into other polyhedra has not been explored. We show here that irregular and regular polyhedra, including some Archimedean and Platonic polyhedra, arise spontaneously in elastic shells formed by more than one component. By formulating a generalized elastic model for inhomogeneous shells, we demonstrate that coassembled shells with two elastic components buckle into polyhedra such as dodecahedra, octahedra, tetrahedra, and hosohedra ...
Highly symmetric nano-shells are found in many biological systems, such as clathrin cages and viral ...
Changes in the geometry and topology of self-assembled membranes underlie diverse processes across c...
he self-assembly and packing of nano-scale particles that have nonspheri-cal shapes is only beginnin...
Large crystalline molecular shells, such as some viruses and fullerenes, buckle spontaneously into i...
The interplay between geometry, topology and order can lead to geometric frustration that profoundly...
Self-organized shells are fundamental in biological compartmentalization. They protect genomic mater...
Minimal energy shapes of closed, elastic shells with twelve pentagonal disclinations introduced in o...
What is the optimal distribution of two types of crystalline phases on the surface of icosahedral sh...
AbstractVirus capsids and crystalline surfactant vesicles are two examples of self-assembled shells ...
Supramolecular constructs that mimic complex biological assemblies are synthetically challenging. He...
We investigate the effects of topological defects on the low-energy shapes of single-component two-d...
Virus capsids and crystalline surfactant vesicles are two examples of self-assembled shells in the n...
While small single-stranded viral shells encapsidate their genome spontaneously, many large viruses,...
AbstractThe lattice model proposed by Lenosky et al. [Nature 355, 333(1992)] have been derived to de...
Highly symmetric nano-shells are found in many biological systems, such as clathrin cages and viral ...
Changes in the geometry and topology of self-assembled membranes underlie diverse processes across c...
he self-assembly and packing of nano-scale particles that have nonspheri-cal shapes is only beginnin...
Large crystalline molecular shells, such as some viruses and fullerenes, buckle spontaneously into i...
The interplay between geometry, topology and order can lead to geometric frustration that profoundly...
Self-organized shells are fundamental in biological compartmentalization. They protect genomic mater...
Minimal energy shapes of closed, elastic shells with twelve pentagonal disclinations introduced in o...
What is the optimal distribution of two types of crystalline phases on the surface of icosahedral sh...
AbstractVirus capsids and crystalline surfactant vesicles are two examples of self-assembled shells ...
Supramolecular constructs that mimic complex biological assemblies are synthetically challenging. He...
We investigate the effects of topological defects on the low-energy shapes of single-component two-d...
Virus capsids and crystalline surfactant vesicles are two examples of self-assembled shells in the n...
While small single-stranded viral shells encapsidate their genome spontaneously, many large viruses,...
AbstractThe lattice model proposed by Lenosky et al. [Nature 355, 333(1992)] have been derived to de...
Highly symmetric nano-shells are found in many biological systems, such as clathrin cages and viral ...
Changes in the geometry and topology of self-assembled membranes underlie diverse processes across c...
he self-assembly and packing of nano-scale particles that have nonspheri-cal shapes is only beginnin...