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

      Journal of the American Chemical Society
      Lead, chemistry, Particle Size, Quantum Dots, Sulfides, chemical synthesis, Surface Properties

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          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.

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          Author and article information

          Journal
          23496143
          10.1021/ja400948t

          Chemistry
          Lead,chemistry,Particle Size,Quantum Dots,Sulfides,chemical synthesis,Surface Properties
          Chemistry
          Lead, chemistry, Particle Size, Quantum Dots, Sulfides, chemical synthesis, Surface Properties

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