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Synthesis of uniform single layer WS(2) for tunable photoluminescence

Two-dimensional transition metal dichalcogenides (2D TMDs) have gained great interest due to their unique tunable bandgap as a function of the number of layers. Especially, single-layer tungsten disulfides (WS(2)) is a direct band gap semiconductor with a gap of 2.1 eV featuring strong photoluminesc...

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Detalles Bibliográficos
Autores principales: Park, Juhong, Kim, Min Su, Cha, Eunho, Kim, Jeongyong, Choi, Wonbong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700996/
https://www.ncbi.nlm.nih.gov/pubmed/29170514
http://dx.doi.org/10.1038/s41598-017-16251-2
Descripción
Sumario:Two-dimensional transition metal dichalcogenides (2D TMDs) have gained great interest due to their unique tunable bandgap as a function of the number of layers. Especially, single-layer tungsten disulfides (WS(2)) is a direct band gap semiconductor with a gap of 2.1 eV featuring strong photoluminescence and large exciton binding energy. Although synthesis of MoS(2) and their layer dependent properties have been studied rigorously, little attention has been paid to the formation of single-layer WS(2) and its layer dependent properties. Here we report the scalable synthesis of uniform single-layer WS(2) film by a two-step chemical vapor deposition (CVD) method followed by a laser thinning process. The PL intensity increases six-fold, while the PL peak shifts from 1.92 eV to 1.97 eV during the laser thinning from few-layers to single-layer. We find from the analysis of exciton complexes that both a neutral exciton and a trion increases with decreasing WS(2) film thickness; however, the neutral exciton is predominant in single-layer WS(2). The binding energies of trion and biexciton for single-layer WS(2) are experimentally characterized at 35 meV and 60 meV, respectively. The tunable optical properties by precise control of WS(2) layers could empower a great deal of flexibility in designing atomically thin optoelectronic devices.