4.8 Article

Assembly of mesoscale helices with near- unity enantiomeric excess and light-matter interactions for chiral semiconductors

Journal

SCIENCE ADVANCES
Volume 3, Issue 3, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.1601159

Keywords

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Funding

  1. NSF project Energy- and Cost-Efficient Manufacturing Employing Nanoparticles [NSF 1463474]
  2. Center for Photonic and Multiscale Nanomaterials - NSF Materials Research Science and Engineering Center program [DMR-1120923]
  3. NSF [1403777, 1411014]
  4. University of Michigan's Michigan Center for Materials Characterization for the NSF [DMR-9871177]
  5. Direct For Mathematical & Physical Scien [1411014] Funding Source: National Science Foundation
  6. Directorate For Engineering [1463474] Funding Source: National Science Foundation
  7. Division Of Materials Research [1411014] Funding Source: National Science Foundation
  8. Div Of Civil, Mechanical, & Manufact Inn [1463474] Funding Source: National Science Foundation

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Semiconductors with chiral geometries at the nanoscale and mesoscale provide a rich materials platform for polarization optics, photocatalysis, and biomimetics. Unlikemetallic and organic opticalmaterials, the relationship between the geometry of chiral semiconductors and their chiroptical properties remains, however, vague. Homochiral ensembles of semiconductor helices with defined geometries open the road to understanding complex relationships between geometrical parameters and chiroptical properties of semiconductormaterials. We showthat semiconductor helices can be prepared with an absolute yield of ca 0.1% and an enantiomeric excess (e.e.) of 98% or above from cysteine-stabilized cadmium telluride nanoparticles (CdTe NPs) dispersed inmethanol. This high e.e. for a spontaneously occurring chemical process is attributed to chiral self-sorting based on the thermodynamic preference of NPs to assemble with those of the same handedness. The dispersions of homochiral self-assembled helices display broadband visible and nearinfrared (Vis-NIR) polarization rotation with anisotropy (g) factors approaching 0.01. Calculated circular dichroism (CD) spectra accurately reproduced experimental CD spectra and gave experimentally validated spectral predictions for different geometrical parameters enabling de novo design of chiroptical semiconductor materials. Unlike metallic, ceramic, and polymeric helices that serve predominantly as scatterers, chiroptical properties of semiconductor helices have nearly equal contribution of light absorption and scattering, which is essential for device-oriented, field-driven light modulation. Deconstruction of a helix into a series of nanorods provides a simple model for the light-matter interaction and chiroptical activity of helices. This study creates a framework for further development of polarizationbased optics toward biomedical applications, telecommunications, and hyperspectral imaging.

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