Your browser doesn't support javascript.
loading
Promoting solution-phase superlattices of CsPbBr3 nanocrystals.
Mireles Villegas, Noel; Hernandez, Josue C; John, Joshua C; Sheldon, Matthew.
Afiliação
  • Mireles Villegas N; Department of Chemistry, Texas A&M University, College Station, Texas 77842, USA. sheldonm@tamu.edu.
  • Hernandez JC; Department of Chemistry, Texas A&M University, College Station, Texas 77842, USA. sheldonm@tamu.edu.
  • John JC; Department of Material Science and Engineering, Texas A&M University, College Station, Texas 77840, USA.
  • Sheldon M; Department of Chemistry, Texas A&M University, College Station, Texas 77842, USA. sheldonm@tamu.edu.
Nanoscale ; 15(22): 9728-9737, 2023 Jun 08.
Article em En | MEDLINE | ID: mdl-37171143
ABSTRACT
We present a size-selective method for purifying and isolating perovskite CsPbBr3 nanocrystals (NCs) that preserves their as-synthesized surface chemistry and extremely high photoluminescence quantum yields (PLQYs). The isolation procedure is based on the stepwise evaporation of nonpolar co-solvents with high vapor pressure to promote precipitation of a size-selected product. As the sample fractions become more uniform in size, we observe that the NCs self-assemble into colloidally stable, solution-phase superlattices (SLs). Small angle X-ray scattering (SAXS) and dynamic light scattering (DLS) studies show that the solution-phase SLs contain 1000s of NCs per supercrystal in a simple cubic, face-to-face packing arrangement. The SLs also display systematically faster radiative decay dynamics and improved PLQYs, as well as unique spectral absorption features likely resulting from inter-particle electronic coupling effects. This study is the first demonstration of solution-phase CsPbBr3 SLs and highlights their potential for achieving collective optoelectronic phenomena previously observed from solid-state assemblies.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article