Tuning of MoS2 Photoluminescence in Heterostructures with CrSBr
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F25%3A00619388" target="_blank" >RIV/61388955:_____/25:00619388 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11320/25:10497960 RIV/60461373:22310/25:43932135 RIV/60461373:22340/25:43932135
Výsledek na webu
<a href="https://hdl.handle.net/11104/0366123" target="_blank" >https://hdl.handle.net/11104/0366123</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acsami.5c01924" target="_blank" >10.1021/acsami.5c01924</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Tuning of MoS2 Photoluminescence in Heterostructures with CrSBr
Popis výsledku v původním jazyce
Monolayers of semiconducting transition metal dichalcogenides (TMDCs) are known for their unique excitonic photoluminescence (PL), which can be tuned by interfacing them with other materials. However, integrating TMDCs into van der Waals heterostructures often results in a significant quenching of the PL because of an increased rate of nonradiative recombination processes. We demonstrate a wide-range tuning of the PL intensity of monolayer MoS2 interfaced with another layered semiconductor, CrSBr. We discover that a thin CrSBr up to approximate to 20 nm in thickness enhances the PL of MoS2, while a thicker material causes PL quenching, which is associated with changes in the excitonic makeup driven by the charge redistribution in the CrSBr/MoS2 heterostructure. Transport measurements, Kelvin probe force microscopy, and first-principles calculations indicate that this charge redistribution most likely causes n- to p-type doping transition of MoS2 upon contact with CrSBr, facilitated by the type II band alignment and the tendency of CrSBr to act as an electron sink. Furthermore, we fabricate an efficient AC-regime photodetector with a responsivity of 10(5) A/W from a MoS2/CrSBr heterostructure.
Název v anglickém jazyce
Tuning of MoS2 Photoluminescence in Heterostructures with CrSBr
Popis výsledku anglicky
Monolayers of semiconducting transition metal dichalcogenides (TMDCs) are known for their unique excitonic photoluminescence (PL), which can be tuned by interfacing them with other materials. However, integrating TMDCs into van der Waals heterostructures often results in a significant quenching of the PL because of an increased rate of nonradiative recombination processes. We demonstrate a wide-range tuning of the PL intensity of monolayer MoS2 interfaced with another layered semiconductor, CrSBr. We discover that a thin CrSBr up to approximate to 20 nm in thickness enhances the PL of MoS2, while a thicker material causes PL quenching, which is associated with changes in the excitonic makeup driven by the charge redistribution in the CrSBr/MoS2 heterostructure. Transport measurements, Kelvin probe force microscopy, and first-principles calculations indicate that this charge redistribution most likely causes n- to p-type doping transition of MoS2 upon contact with CrSBr, facilitated by the type II band alignment and the tendency of CrSBr to act as an electron sink. Furthermore, we fabricate an efficient AC-regime photodetector with a responsivity of 10(5) A/W from a MoS2/CrSBr heterostructure.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10403 - Physical chemistry
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
ACS Applied Materials and Interfaces
ISSN
1944-8244
e-ISSN
1944-8252
Svazek periodika
17
Číslo periodika v rámci svazku
17
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
9
Strana od-do
25693-25701
Kód UT WoS článku
001468413600001
EID výsledku v databázi Scopus
2-s2.0-105004049535