4.8 Article

Small-Angle X-ray Scattering Analysis of Colloidal Crystals and Replica Materials Made from L-Arginine-Stabilized Silica

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 7, Pages 9398-9407

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c19193

Keywords

silica nanoparticles; assembly; three-dimensional nanostructures; templates; high-pressure deposition; small-angle X-ray scattering; long-range order; L-arginine-stabilized silica; evaporative colloidal crystal growth

Funding

  1. National Science Foundation under MRSEC [DMR1420620]
  2. DOE Office of Science [DE-AC02-06CH11357]

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This study investigated the structures of colloidal crystals made from sub-100 nm silica nanoparticles and revealed that the structure depends on particle size. The structure of these materials remains intact under high temperature and pressure, with factors like shear force during deposition and dispersity of silica nanoparticles influencing the size of crystal domains in the films.
Colloidal crystals made from sub-100 nm silica nanoparticles have provided a versatile platform for the template-assisted synthesis of three-dimensionally interconnected semiconducting, metallic, and magnetic replicas. However, the detailed structure of these materials has not yet been characterized. In this study, we investigated the structures of colloidal crystalline films and germanium replicas by scanning electron microscopy and small angle X-ray scattering. The structures of colloidal crystals made by evaporative assembly depends on the size of L-arginine-capped silica nanoparticles. Particles smaller than similar to 31 nm diameter assemble into non-close-packed arrangements (bcc) whereas particles larger than 31 nm assemble into random close-packed structures with disordered hexagonal phase. Polycrystalline films of these materials retain their structures and long-range order upon infiltration at high temperature and pressure, and the structure is preserved in Ge replicas. The shear force during deposition and dispersity of silica nanoparticles contributes to the size-based variation in the structure and to the size of crystal domains in the colloidal crystal films.

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