Abstract

The low light absorption of transition-metal dichalcogenide (TMDC) nanosheets hinders their application as high-performance optoelectronic devices. Rolling them up into one-dimensional (1D) nanoscrolls and decorating them with plasmonic nanoparticles (NPs) are both effective strategies for enhancing their performance. When these two approaches are combined, in this work, the light-matter interaction in TMDC nanosheets is greatly improved by encapsulating silver nanoparticles (Ag NPs) in TMDC nanoscrolls. After the silver nitrate (AgNO3) solution was spin-coated on monolayer (1L) MoS2 and WS2 nanosheets grown by chemical vapor deposition, Ag NPs were homogeneously formed to obtain MoS2-Ag and WS2-Ag nanosheets due to the TMDC-assisted spontaneous reduction, and their size and density can be well controlled by tuning the concentration of the AgNO3 solution. By the simple placement of alkaline droplets on MoS2-Ag or WS2-Ag hybrid nanosheets, MoS2-Ag or WS2-Ag nanoscrolls with large sizes were obtained in large area. The obtained hybrid nanoscrolls exhibited up to 500 times increased photosensitivities compared with 1L MoS2 nanosheets, arising from the localized surface plasmon resonance effect of Ag NPs and the scrolled-nanosheet structure. Our work provides a reliable method for the facile and large-area preparation of NP/nanosheet hybrid nanoscrolls and demonstrates their great potential for high-performance optoelectronic devices.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.