4.8 Article

Colloidal Self-Assembly-Directed Laser-Induced Non-Close-Packed Crystalline Silicon Nanostructures

Journal

ACS NANO
Volume 5, Issue 10, Pages 7960-7966

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn2023446

Keywords

self-assembly; pulsed laser irradiation; colloidal crystals; silicon; crystalline; non-close-packed

Funding

  1. NSF [DMR-0605856]
  2. U.S. Department of Homeland Security [2009-ST-108-LR0004]
  3. Singapore Energy Innovation Programme Office
  4. Intel Foundation for an Engineering Learning Initiatives
  5. Panasonic Corporation
  6. Materials Research Science and Engineering Center of NSF [DMR-0520404]
  7. Cornell Nanoscale Science and Technology Facility by NSF [ECS-0335765]
  8. Direct For Mathematical & Physical Scien
  9. Division Of Materials Research [1120296] Funding Source: National Science Foundation

Ask authors/readers for more resources

This report describes an ultrafast, large-area, and highly flexible method to construct complex two- and three-dimensional silicon nanostructures with deterministic non-close-packed symmetry. Pulsed excimer laser irradiation is used to induce a transient melt transformation of amorphous silicon filled in a colloidal self-assembly-directed Inverse opal template, resulting in a nanostructured crystalline phase. The pattern transfer yields are high, and long-range order Is maintained. This technique represents a potential route to obtain silicon nanostructures of various symmetries and associated unique Properties for advanced applications such as energy storage and generation.

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