Steric-hindrance-driven shape transition in PbS quantum dots: understanding size-dependent stability

J Am Chem Soc. 2013 Apr 10;135(14):5278-81. doi: 10.1021/ja400948t. Epub 2013 Mar 27.

Abstract

Ambient stability of colloidal nanocrystal quantum dots (QDs) is imperative for low-cost, high-efficiency QD photovoltaics. We synthesized air-stable, ultrasmall PbS QDs with diameter (D) down to 1.5 nm, and found an abrupt transition at D ≈ 4 nm in the air stability as the QD size was varied from 1.5 to 7.5 nm. X-ray photoemission spectroscopy measurements and density functional theory calculations reveal that the stability transition is closely associated with the shape transition of oleate-capped QDs from octahedron to cuboctahedron, driven by steric hindrance and thus size-dependent surface energy of oleate-passivated Pb-rich QD facets. This microscopic understanding of the surface chemistry on ultrasmall QDs, up to a few nanometers, should be very useful for precisely and accurately controlling physicochemical properties of colloidal QDs such as doping polarity, carrier mobility, air stability, and hot-carrier dynamics for solar cell applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Lead / chemistry*
  • Particle Size
  • Quantum Dots*
  • Sulfides / chemical synthesis
  • Sulfides / chemistry*
  • Surface Properties

Substances

  • Sulfides
  • lead sulfide
  • Lead