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Understanding the Structural Origin of Chirality in Magic-Size Semiconductor Nanoclusters through Self-Assembly
Hongjin Du1, Ellery J Hendrix1, Richard D Robinson1
1Department of Materials Science and Engineering, Cornell University, Ithaca, New York 14853, United States.
None:
Semiconductor magic-size clusters (MSCs) are atomically precise nanoparticles exhibiting unique size-dependent properties, but their ultrasmall dimensions hinder structural characterization, limiting our understanding of their formation and stability. A few MSC structures have been fully resolved, revealing either bulk-like zincblende-type structures or a range of nonbulk-like motifs. Here we use a computational model to investigate the relationship between the cluster size and atomic structure in zincblende-forming II-VI and III-V semiconductors. First, we find that all nonbulk-like MSCs in these systems exhibit the same distorted icosahedral motif that is intrinsically chiral. Second, we reproduce these MSC geometries in small-cluster self-assembly simulations and discover that their chirality emerges from the geometric frustration and symmetry breaking in arranging tetrahedral bonding environments into an icosahedral topology. Overall, this work reproduces experimentally reported motifs without system-specific parametrization, establishes the structural origin of chirality in MSCs, and provides design principles for predicting new cluster geometries.
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