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Suppression of Defects and Deep Levels Using Isoelectronic Tungsten Substitution in Monolayer MoSe2

Defects formed during chemical vapor deposition (CVD) of two‐dimensional (2D) transition metal dichalcogenides (TMDs) currently limit their quality and optoelectronic properties. Effective synthesis and processing strategies to suppress defects and enhance the quality of 2D TMDs are urgently needed...

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Published in:Advanced functional materials 2017-05, Vol.27 (19), p.n/a
Main Authors: Li, Xufan, Puretzky, Alexander A., Sang, Xiahan, KC, Santosh, Tian, Mengkun, Ceballos, Frank, Mahjouri‐Samani, Masoud, Wang, Kai, Unocic, Raymond R., Zhao, Hui, Duscher, Gerd, Cooper, Valentino R., Rouleau, Christopher M., Geohegan, David B., Xiao, Kai
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container_issue 19
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container_title Advanced functional materials
container_volume 27
creator Li, Xufan
Puretzky, Alexander A.
Sang, Xiahan
KC, Santosh
Tian, Mengkun
Ceballos, Frank
Mahjouri‐Samani, Masoud
Wang, Kai
Unocic, Raymond R.
Zhao, Hui
Duscher, Gerd
Cooper, Valentino R.
Rouleau, Christopher M.
Geohegan, David B.
Xiao, Kai
description Defects formed during chemical vapor deposition (CVD) of two‐dimensional (2D) transition metal dichalcogenides (TMDs) currently limit their quality and optoelectronic properties. Effective synthesis and processing strategies to suppress defects and enhance the quality of 2D TMDs are urgently needed to enable next generation optoelectronic devices. In this work, isoelectronic doping is presented as a new strategy to form stable alloys and suppress defects and enhance photoluminescence (PL) in CVD‐grown TMD monolayers. The isoelectronic substitution of W atoms for Mo atoms in CVD‐grown monolayers of Mo1– x W x Se2 (0 < x < 0.18) is shown to effectively suppress Se vacancy concentration by 50% compared to those found in pristine MoSe2 monolayers, resulting in a decrease in defect‐mediated nonradiative recombination, ≈10 times more intense PL, and an increase in the carrier lifetime by a factor of 3. Theoretical predictions reveal that isoelectronic W alloying to form Mo1– x W x Se2 monolayers raises the energy of deep level defects in MoSe2 to enable faster quenching, which is confirmed by low temperature (4–125 K) PL from defect‐related localized states. Isoelectronic substitution therefore appears to be a promising synthetic method to control the heterogeneity of 2D TMDs to realize the scalable production of high performance optoelectronic and electronic devices. Isoelectronic tungsten alloying in MoSe2 monolayers, forming Mo1– x W x Se2, suppresses both the formation of Se vacancies in the lattice and the deep levels in the electronic bandgap. As a result, the photoluminescence is greatly enhanced by up to 10 times.
doi_str_mv 10.1002/adfm.201603850
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Center for Nanophase Materials Sciences (CNMS)</creatorcontrib><description>Defects formed during chemical vapor deposition (CVD) of two‐dimensional (2D) transition metal dichalcogenides (TMDs) currently limit their quality and optoelectronic properties. Effective synthesis and processing strategies to suppress defects and enhance the quality of 2D TMDs are urgently needed to enable next generation optoelectronic devices. In this work, isoelectronic doping is presented as a new strategy to form stable alloys and suppress defects and enhance photoluminescence (PL) in CVD‐grown TMD monolayers. The isoelectronic substitution of W atoms for Mo atoms in CVD‐grown monolayers of Mo1– x W x Se2 (0 &lt; x &lt; 0.18) is shown to effectively suppress Se vacancy concentration by 50% compared to those found in pristine MoSe2 monolayers, resulting in a decrease in defect‐mediated nonradiative recombination, ≈10 times more intense PL, and an increase in the carrier lifetime by a factor of 3. Theoretical predictions reveal that isoelectronic W alloying to form Mo1– x W x Se2 monolayers raises the energy of deep level defects in MoSe2 to enable faster quenching, which is confirmed by low temperature (4–125 K) PL from defect‐related localized states. Isoelectronic substitution therefore appears to be a promising synthetic method to control the heterogeneity of 2D TMDs to realize the scalable production of high performance optoelectronic and electronic devices. Isoelectronic tungsten alloying in MoSe2 monolayers, forming Mo1– x W x Se2, suppresses both the formation of Se vacancies in the lattice and the deep levels in the electronic bandgap. 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The isoelectronic substitution of W atoms for Mo atoms in CVD‐grown monolayers of Mo1– x W x Se2 (0 &lt; x &lt; 0.18) is shown to effectively suppress Se vacancy concentration by 50% compared to those found in pristine MoSe2 monolayers, resulting in a decrease in defect‐mediated nonradiative recombination, ≈10 times more intense PL, and an increase in the carrier lifetime by a factor of 3. Theoretical predictions reveal that isoelectronic W alloying to form Mo1– x W x Se2 monolayers raises the energy of deep level defects in MoSe2 to enable faster quenching, which is confirmed by low temperature (4–125 K) PL from defect‐related localized states. Isoelectronic substitution therefore appears to be a promising synthetic method to control the heterogeneity of 2D TMDs to realize the scalable production of high performance optoelectronic and electronic devices. Isoelectronic tungsten alloying in MoSe2 monolayers, forming Mo1– x W x Se2, suppresses both the formation of Se vacancies in the lattice and the deep levels in the electronic bandgap. As a result, the photoluminescence is greatly enhanced by up to 10 times.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/adfm.201603850</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Carrier lifetime
Chemical vapor deposition
Defects
Doping
Electronic devices
Heterogeneity
isoelectronic
MATERIALS SCIENCE
Mo1–xWxSe2
Monolayers
Optoelectronic devices
Photoluminescence
Quenching
Tungsten base alloys
Vacancies
title Suppression of Defects and Deep Levels Using Isoelectronic Tungsten Substitution in Monolayer MoSe2
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