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  5. Upconverted electroluminescence via Auger scattering of interlayer excitons in van der Waals heterostructures

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Article
English
2019

Upconverted electroluminescence via Auger scattering of interlayer excitons in van der Waals heterostructures

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English
2019
Nature Communications
Vol 10 (1)
DOI: 10.1038/s41467-019-10323-9

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Konstantin ‘kostya’  Novoselov
Konstantin ‘kostya’ Novoselov

The University of Manchester

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Johannes Binder
James Howarth
F. Withers
+11 more

Abstract

The intriguing physics of carrier-carrier interactions, which likewise affect the operation of light emitting devices, stimulate the research on semiconductor structures at high densities of excited carriers, a limit reachable at large pumping rates or in systems with long-lived electron-hole pairs. By electrically injecting carriers into WSe$_2$/MoS$_2$ type-II heterostructures which are indirect in real and k-space, we establish a large population of typical optically silent interlayer excitons. Here, we reveal their emission spectra and show that the emission energy is tunable by an applied electric field. When the population is further increased by suppressing the radiative recombination rate with the introduction of an hBN spacer between WSe$_2$ and MoS$_2$, Auger-type and exciton-exciton annihilation processes become important. These processes are traced by the observation of an up-converted emission demonstrating that excitons gaining energy in non-radiative Auger processes can be recovered and recombine radiatively.

How to cite this publication

Johannes Binder, James Howarth, F. Withers, Maciej R. Molas, Takashi Taniguchi, Kenji Watanabe, C. Faugeras, A. Wysmołek, Mark Danovich, Vladimir I. Fal’ko, A. K. Geǐm, Konstantin ‘kostya’ Novoselov, M. Potemski, Aleksey Kozikov (2019). Upconverted electroluminescence via Auger scattering of interlayer excitons in van der Waals heterostructures. Nature Communications, 10(1), DOI: 10.1038/s41467-019-10323-9.

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Publication Details

Type

Article

Year

2019

Authors

14

Datasets

0

Total Files

0

Language

English

Journal

Nature Communications

DOI

10.1038/s41467-019-10323-9

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