4.8 Article

Collective topo-epitaxy in the self-assembly of a 3D quantum dot superlattice

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NATURE MATERIALS
卷 19, 期 1, 页码 49-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41563-019-0485-2

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资金

  1. UC Office of the President under the UC Laboratory Fees Research Program Collaborative Research and Training Award [LFR-17-477148]
  2. DOE Office of Science User Facility [DE-AC02-05CH11231]
  3. National Science Foundation [CHE-1338173]

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Epitaxially fused colloidal quantum dot (QD) superlattices (epi-SLs) may enable a new class of semiconductors that combine the size-tunable photophysics of QDs with bulk-like electronic performance, but progress is hindered by a poor understanding of epi-SL formation and surface chemistry. Here we use X-ray scattering and correlative electron imaging and diffraction of individual SL grains to determine the formation mechanism of three-dimensional PbSe QD epi-SL films. We show that the epi-SL forms from a rhombohedrally distorted body centred cubic parent SL via a phase transition in which the QDs translate with minimal rotation (similar to 10 degrees) and epitaxially fuse across their {100} facets in three dimensions. This collective epitaxial transformation is atomically topotactic across the 10(3)-10(5) QDs in each SL grain. Infilling the epi-SLs with alumina by atomic layer deposition greatly changes their electrical properties without affecting the superlattice structure. Our work establishes the formation mechanism of three-dimensional QD epi-SLs and illustrates the critical importance of surface chemistry to charge transport in these materials.

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