Apr 24, 2024
11:15am - 11:30am
Room 344, Level 3, Summit
Boxuan Zhou1,Jingyuan Zhou1,Xiangfeng Duan1
University of California Los Angeles1
Boxuan Zhou1,Jingyuan Zhou1,Xiangfeng Duan1
University of California Los Angeles1
<b>Molybdenum disulfide (MoS<sub>2</sub>) is an extensively studied two-dimensional layered semiconductor with interesting electronic and optical properties. Monolayer MoS<sub>2</sub> features strong light-matter interactions due to its direct bandgap, whereas multilayer MoS<sub>2 </sub>is an indirect bandgap semiconductor and optically inactive. The molecular intercalation of MoS<sub>2</sub> with organic cations offers a strategy to decouple the interlayer interaction, producing a bulk monolayer material, but is usually accompanied by a heavy electron doping effect that can diminish the intrinsic semiconductor properties or induce a phase transition. Herein, we report a chemical-dedoping strategy to tailor electron density in molecular-intercalated MoS<sub>2,</sub> therefore retaining monolayer properties. By introducing a poly(vinylpyrrolidone)-bromine complex during the electrochemical intercalation process, we show bulk monolayer MoS<sub>2</sub> thin film can be produced with decoupled interlayer interaction and reduced electron concentration. The resulting thin films display strong excitonic emission, 20- and > 400 times stronger than the exfoliated monolayer and multilayer material respectively, as well as high valley polarization and enhanced photo-electric response. Our study opens a scalable path to large-area bulk monolayer MoS<sub>2</sub> thin films with monolayer-like optical properties and greatly increased optical cross-section, presenting an attractive material platform for both fundamental photophysics studies and scalable optoelectronic applications.</b>