11:30 AM - 11:45 AM
▲ [20a-E319-7] In situ work function measurement in the transformation of MoS2 to MoO3 using ambient pressure X-ray photoelectron spectroscopy
Keywords:Ambient pressure X-ray photoelectron spectroscopy, Work function, Chemical transformation
Chemical transformation of low-dimensional (2D) materials is useful in further expanding 2D material to realize layered transition metal oxides and their heterojunction. Recently, there have been few reports on a layered MoO3 and a heterostructure MoO3/MoS2 from chemical transformation of MoS2. However, the difficult to obtain the high-quality MoO3/MoS2 remained because there are unexpected sub-oxide defects (i.e., MoSxO1-x) during chemical transformation. Therefore, it is important to monitor the change in physical and chemical properties during the chemical transformation, simultaneously.
In this presentation, we showed the experimental result of the in-situ work function and the chemical state of MoS2 under chemical transformation using the ambient pressure X-ray photoelectron spectroscopy. The chemical transformation of MoS2 was performed under annealing temperature (RT ~ 350 oC) in 1 mbar O2 gas +1 mbar Ar gas. As a result, we found that the chemical state of MoS2 was unchanged. However, the work function increased owing to the decrease in carbon/H2O contamination from RT to 200 oC. Further increased temperature, the MoS2 partially transformed into MoO3, resulting in the increased work function. At 350 oC, MoS2 completely disappeared, and MoO3 was formed. These results will provide a way for precise control of chemical transformation of 2D materials by in situ monitoring the physical and chemical properties.
In this presentation, we showed the experimental result of the in-situ work function and the chemical state of MoS2 under chemical transformation using the ambient pressure X-ray photoelectron spectroscopy. The chemical transformation of MoS2 was performed under annealing temperature (RT ~ 350 oC) in 1 mbar O2 gas +1 mbar Ar gas. As a result, we found that the chemical state of MoS2 was unchanged. However, the work function increased owing to the decrease in carbon/H2O contamination from RT to 200 oC. Further increased temperature, the MoS2 partially transformed into MoO3, resulting in the increased work function. At 350 oC, MoS2 completely disappeared, and MoO3 was formed. These results will provide a way for precise control of chemical transformation of 2D materials by in situ monitoring the physical and chemical properties.