Biexciton Formation in Bilayer Tungsten Disulfide

Monolayer transition metal dichalcogenides (TMDs) are direct band gap semiconductors, and their 2D structure results in large binding energies for excitons, trions, and biexcitons. The ability to explore many-body effects in these monolayered structures has made them appealing for future optoelectro...

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Main Authors: He, Z, Xu, W, Zhou, Y, Wang, X, Sheng, Y, Rong, Y, Guo, S, Zhang, J, Smith, J, Warner, J
Format: Journal article
Language:English
Published: American Chemical Society 2016
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author He, Z
Xu, W
Zhou, Y
Wang, X
Sheng, Y
Rong, Y
Guo, S
Zhang, J
Smith, J
Warner, J
author_facet He, Z
Xu, W
Zhou, Y
Wang, X
Sheng, Y
Rong, Y
Guo, S
Zhang, J
Smith, J
Warner, J
author_sort He, Z
collection OXFORD
description Monolayer transition metal dichalcogenides (TMDs) are direct band gap semiconductors, and their 2D structure results in large binding energies for excitons, trions, and biexcitons. The ability to explore many-body effects in these monolayered structures has made them appealing for future optoelectronic and photonic applications. The band structure changes for bilayer TMDs with increased contributions from indirect transitions, and this has limited similar in-depth studies of biexcitons. Here, we study biexciton emission in bilayer WS2 grown by chemical vapor deposition as a function of temperature. A biexciton binding energy of 36 �4 meV is measured in the as-grown bilayer WS2 containing 0.4% biaxial strain as determined by Raman spectroscopy. The biexciton emission was difficult to detect when the WS2 was transferred to another substrate to release the stain. Density functional theory calculations show that 0.4% of tensile strain lowers the direct band gap by about 55 meV without significant change to the indirect band gap, which can cause an increase in the quantum yield of direct exciton transitions and the emission from biexcitons formed by two direct gap excitons. We find that the biexciton emission decreases dramatically with increased temperature due to the thermal dissociation, with an activation energy of 26 � 5 meV. These results show how strain can be used to tune the many-body effects in bilayered TMD materials and extend the photonic applications beyond pure monolayer systems.
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spelling oxford-uuid:b12ec354-6ea7-4017-aed4-64d96d0bed2a2022-03-27T04:02:10ZBiexciton Formation in Bilayer Tungsten DisulfideJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b12ec354-6ea7-4017-aed4-64d96d0bed2aEnglishSymplectic Elements at OxfordAmerican Chemical Society2016He, ZXu, WZhou, YWang, XSheng, YRong, YGuo, SZhang, JSmith, JWarner, JMonolayer transition metal dichalcogenides (TMDs) are direct band gap semiconductors, and their 2D structure results in large binding energies for excitons, trions, and biexcitons. The ability to explore many-body effects in these monolayered structures has made them appealing for future optoelectronic and photonic applications. The band structure changes for bilayer TMDs with increased contributions from indirect transitions, and this has limited similar in-depth studies of biexcitons. Here, we study biexciton emission in bilayer WS2 grown by chemical vapor deposition as a function of temperature. A biexciton binding energy of 36 �4 meV is measured in the as-grown bilayer WS2 containing 0.4% biaxial strain as determined by Raman spectroscopy. The biexciton emission was difficult to detect when the WS2 was transferred to another substrate to release the stain. Density functional theory calculations show that 0.4% of tensile strain lowers the direct band gap by about 55 meV without significant change to the indirect band gap, which can cause an increase in the quantum yield of direct exciton transitions and the emission from biexcitons formed by two direct gap excitons. We find that the biexciton emission decreases dramatically with increased temperature due to the thermal dissociation, with an activation energy of 26 � 5 meV. These results show how strain can be used to tune the many-body effects in bilayered TMD materials and extend the photonic applications beyond pure monolayer systems.
spellingShingle He, Z
Xu, W
Zhou, Y
Wang, X
Sheng, Y
Rong, Y
Guo, S
Zhang, J
Smith, J
Warner, J
Biexciton Formation in Bilayer Tungsten Disulfide
title Biexciton Formation in Bilayer Tungsten Disulfide
title_full Biexciton Formation in Bilayer Tungsten Disulfide
title_fullStr Biexciton Formation in Bilayer Tungsten Disulfide
title_full_unstemmed Biexciton Formation in Bilayer Tungsten Disulfide
title_short Biexciton Formation in Bilayer Tungsten Disulfide
title_sort biexciton formation in bilayer tungsten disulfide
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