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Colloidal nanocrystal heterostructures with linear and branched topology

Author

Listed:
  • Delia J. Milliron

    (University of California
    University of California)

  • Steven M. Hughes

    (University of California
    University of California)

  • Yi Cui

    (University of California
    University of California)

  • Liberato Manna

    (University of California
    University of California
    National Nanotechnology Lab of INFM)

  • Jingbo Li

    (Lawrence Berkeley National Laboratory)

  • Lin-Wang Wang

    (Lawrence Berkeley National Laboratory)

  • A. Paul Alivisatos

    (University of California
    University of California)

Abstract

The development of colloidal quantum dots has led to practical applications of quantum confinement, such as in solution-processed solar cells1, lasers2 and as biological labels3. Further scientific and technological advances should be achievable if these colloidal quantum systems could be electronically coupled in a general way. For example, this was the case when it became possible to couple solid-state embedded quantum dots into quantum dot molecules4,5. Similarly, the preparation of nanowires with linear alternating compositions—another form of coupled quantum dots—has led to the rapid development of single-nanowire light-emitting diodes6 and single-electron transistors7. Current strategies to connect colloidal quantum dots use organic coupling agents8,9, which suffer from limited control over coupling parameters and over the geometry and complexity of assemblies. Here we demonstrate a general approach for fabricating inorganically coupled colloidal quantum dots and rods, connected epitaxially at branched and linear junctions within single nanocrystals. We achieve control over branching and composition throughout the growth of nanocrystal heterostructures to independently tune the properties of each component and the nature of their interactions. Distinct dots and rods are coupled through potential barriers of tuneable height and width, and arranged in three-dimensional space at well-defined angles and distances. Such control allows investigation of potential applications ranging from quantum information processing to artificial photosynthesis.

Suggested Citation

  • Delia J. Milliron & Steven M. Hughes & Yi Cui & Liberato Manna & Jingbo Li & Lin-Wang Wang & A. Paul Alivisatos, 2004. "Colloidal nanocrystal heterostructures with linear and branched topology," Nature, Nature, vol. 430(6996), pages 190-195, July.
  • Handle: RePEc:nat:nature:v:430:y:2004:i:6996:d:10.1038_nature02695
    DOI: 10.1038/nature02695
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    Cited by:

    1. Michele Ghini & Nicola Curreli & Matteo B. Lodi & Nicolò Petrini & Mengjiao Wang & Mirko Prato & Alessandro Fanti & Liberato Manna & Ilka Kriegel, 2022. "Control of electronic band profiles through depletion layer engineering in core–shell nanocrystals," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    2. Xiaohua Liu & Yongjing Lin & Sa Zhou & Stafford Sheehan & Dunwei Wang, 2010. "Complex Nanostructures: Synthesis and Energetic Applications," Energies, MDPI, vol. 3(3), pages 1-16, February.
    3. Qing-Xia Chen & Yu-Yang Lu & Yang Yang & Li-Ge Chang & Yi Li & Yuan Yang & Zhen He & Jian-Wei Liu & Yong Ni & Shu-Hong Yu, 2024. "Stress-induced ordering evolution of 1D segmented heteronanostructures and their chemical post-transformations," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

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