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Moungi G. Bawendi

Researcher at Massachusetts Institute of Technology

Publications -  650
Citations -  128860

Moungi G. Bawendi is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Quantum dot & Nanocrystal. The author has an hindex of 165, co-authored 626 publications receiving 118108 citations. Previous affiliations of Moungi G. Bawendi include United States Department of the Navy & United States Naval Research Laboratory.

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Water-soluble fluorescent semiconductor nanocrystals

TL;DR: In this paper, a water-soluble semiconductor nanocrystal capable of light emission is provided, including a semiconductor core having a selected band gap energy, a shell layer overcoating the core, and an outer layer comprised of a molecule having at least one linking group for attachment of the molecule to the shell layer.
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Engineering InAs(x)P(1-x)/InP/ZnSe III-V alloyed core/shell quantum dots for the near-infrared.

TL;DR: Quantum dots with a core/shell/shell structure consisting of an alloyed core of InAs(x)P(1-x), an intermediate shell of InP, and an outer shell of ZnSe were developed and successfully used in a sentinel lymph node mapping experiment.
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Mechanisms for intraband energy relaxation in semiconductor quantum dots: The role of electron-hole interactions

TL;DR: In this article, the role of electron-hole (e-h) interactions in quantum dots has been investigated and it has been shown that electron relaxation is dominated not by phonon emission but by the e-h energy transfer.
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NiO as an inorganic hole-transporting layer in quantum-dot light-emitting devices.

TL;DR: A hybrid inorganic/organic light-emitting device composed of a CdSe/ZnS core/shell semiconductor quantum-dot emissive layer sandwiched between p-type NiO and tris-(8-hydroxyquinoline) aluminum (Alq3), as hole and electron transporting layers, respectively is demonstrated.
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Energy harvesting of non-emissive triplet excitons in tetracene by emissive PbS nanocrystals

TL;DR: Direct excitonic energy transfer from 'dark' triplets in the organic semiconductor tetracene to colloidal PbS nanocrystals is demonstrated, thereby successfully harnessing molecular triplet excitons in the near infrared and may permit singlet exciton fission sensitization of conventional silicon solar cells.