4.7 Article

Role of shell composition and morphology in achieving single-emitter photostability for green-emitting giant quantum dots

Journal

JOURNAL OF CHEMICAL PHYSICS
Volume 152, Issue 12, Pages -

Publisher

AMER INST PHYSICS
DOI: 10.1063/5.0002772

Keywords

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Funding

  1. U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy (EERE) [M615002955]
  2. Laboratory Directed Research and Development (LDRD) program at Los Alamos National Laboratory [20170001DR]
  3. National Science Foundation CHE [1506587]
  4. U.S. Department of Energy, Materials Sciences and Engineering Division
  5. National Nuclear Security Administration of the U.S. Department of Energy [DE-AC52-06NA25396]
  6. Division Of Chemistry
  7. Direct For Mathematical & Physical Scien [1506587] Funding Source: National Science Foundation

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The use of the varied chemical reactivity of precursors to drive the production of a desired nanocrystal architecture has become a common method to grow thick-shell graded alloy quantum dots (QDs) with robust optical properties. Conclusions on their behavior assume the ideal chemical gradation and uniform particle composition. Here, advanced analytical electron microscopy (high-resolution scanning transmission electron microscopy coupled with energy dispersive spectroscopy) is used to confirm the nature and extent of compositional gradation and these data are compared with performance behavior obtained from single-nanocrystal spectroscopy to elucidate structure, chemical-composition, and optical-property correlations. Specifically, the evolution of the chemical structure and single-nanocrystal luminescence was determined for a time-series of graded-alloy CdZnSSe/ZnS core/shell QDs prepared in a single-pot reaction. In a separate step, thick (similar to 6 monolayers) to giant (>14 monolayers) shells of ZnS were added to the alloyed QDs via a successive ionic layer adsorption and reaction (SILAR) process, and the impact of this shell on the optical performance was also assessed. By determining the degree of alloying for each component element on a per-particle basis, we observe that the actual product from the single-pot reaction is less graded in Cd and more so in Se than anticipated, with Se extending throughout the structure. The latter suggests much slower Se reaction kinetics than expected or an ability of Se to diffuse away from the initially nucleated core. It was also found that the subsequent growth of thick phase-pure ZnS shells by the SILAR method was required to significantly reduce blinking and photobleaching. However, correlated single-nanocrystal optical characterization and electron microscopy further revealed that these beneficial properties are only achieved if the thick ZnS shell is complete and without large lattice discontinuities. In this way, we identify the necessary structural design features that are required for ideal light emission properties in these green-visible emitting QDs.

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