Abstract:Transition metal dichalcogenide (TMD) monolayers and their heterostructures have attracted considerable attention due to their distinct properties. In this work, we performed a systematic investigation of MoS2/WSe2 heterostructures, focusing on their temperature-dependent Raman and photoluminescence (PL) characteristics in the range of 79 to 473 K. Our Raman analysis revealed that both the longitudinal and transverse modes of the heterostructure exhibit linear shifts towards low frequencies with increasing tem… Show more
“…As observed in Figure a, in the case of the bare WSe 2 , its PL undergoes a red-shift and thermal quenching as the temperature increases from −120 to 120 °C, which can be attributed to enhanced electron–phonon coupling and nonradiative recombination. The observation aligns with the temperature characteristics commonly observed in 2D semiconductors. , In the case of the TiOPc/WSe 2 , the emission peak position at 1.53 eV remains almost unchanged with the temperature increases from −120 to 120 °C. However, its intensity is gradually reduced, suggesting significant thermal quenching occurs.…”
Section: Resultssupporting
confidence: 88%
“…The observation aligns with the temperature characteristics commonly observed in 2D semiconductors. 51,52 In the case of the TiOPc/WSe 2 , the emission peak position at 1.53 eV remains almost unchanged with the temperature increases from −120 to 120 °C. However, its intensity is gradually reduced, suggesting significant thermal quenching occurs.…”
The van der Waals (vdW) heterostructures composed of twodimensional (2D) transition metal dichalcogenides (TMDs) and organic semiconductors demonstrate numerous compelling optoelectronic properties. However, the influence of the vdW epitaxial effect and temperature on the optoelectronic properties and interface exciton dynamics of heterostructures remains unclear. This study systematically investigates the fluorescence properties of TiOPc/WSe 2 heterostructure. Comprehensive spectral characterization elucidates that the emission behavior of the TiOPc/WSe 2 heterostructure arises from charge/energy transfer at the heterostructure interfaces and the structural ordering of the organic layer on the 2D monolayer WSe 2 induced by vdW epitaxy. The interface exciton dynamic features probed by ultrafast transient spectroscopy reveal that the face-to-face molecular stacking configuration of TiOPc exhibits ultrafast exciton dynamics. In particular, we observe picosecond-scale absorption of organic molecular dimer cations, providing direct evidence of interface charge transfer at room temperature. Moreover, energy transfer from the TiOPc to WSe 2 may exist based on the tunability in the fluorescence emission of the TiOPc/WSe 2 heterostructure as the temperature changes. This study unveils the critical role of vdW epitaxy and temperature in the exciton dynamics of organic/2D TMDs hybrid systems and provides guidance for studying interlayer charge and energy transfer in organic/inorganic heterostructures.
“…As observed in Figure a, in the case of the bare WSe 2 , its PL undergoes a red-shift and thermal quenching as the temperature increases from −120 to 120 °C, which can be attributed to enhanced electron–phonon coupling and nonradiative recombination. The observation aligns with the temperature characteristics commonly observed in 2D semiconductors. , In the case of the TiOPc/WSe 2 , the emission peak position at 1.53 eV remains almost unchanged with the temperature increases from −120 to 120 °C. However, its intensity is gradually reduced, suggesting significant thermal quenching occurs.…”
Section: Resultssupporting
confidence: 88%
“…The observation aligns with the temperature characteristics commonly observed in 2D semiconductors. 51,52 In the case of the TiOPc/WSe 2 , the emission peak position at 1.53 eV remains almost unchanged with the temperature increases from −120 to 120 °C. However, its intensity is gradually reduced, suggesting significant thermal quenching occurs.…”
The van der Waals (vdW) heterostructures composed of twodimensional (2D) transition metal dichalcogenides (TMDs) and organic semiconductors demonstrate numerous compelling optoelectronic properties. However, the influence of the vdW epitaxial effect and temperature on the optoelectronic properties and interface exciton dynamics of heterostructures remains unclear. This study systematically investigates the fluorescence properties of TiOPc/WSe 2 heterostructure. Comprehensive spectral characterization elucidates that the emission behavior of the TiOPc/WSe 2 heterostructure arises from charge/energy transfer at the heterostructure interfaces and the structural ordering of the organic layer on the 2D monolayer WSe 2 induced by vdW epitaxy. The interface exciton dynamic features probed by ultrafast transient spectroscopy reveal that the face-to-face molecular stacking configuration of TiOPc exhibits ultrafast exciton dynamics. In particular, we observe picosecond-scale absorption of organic molecular dimer cations, providing direct evidence of interface charge transfer at room temperature. Moreover, energy transfer from the TiOPc to WSe 2 may exist based on the tunability in the fluorescence emission of the TiOPc/WSe 2 heterostructure as the temperature changes. This study unveils the critical role of vdW epitaxy and temperature in the exciton dynamics of organic/2D TMDs hybrid systems and provides guidance for studying interlayer charge and energy transfer in organic/inorganic heterostructures.
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