Abstract

Molybdenum disulfide (MoS2) is a two-dimensional material promising for electronic, optical, and catalytic applications. To fully harness its potential, functionalization is essential to controlling its properties. However, MoS2 functionalization has been mostly limited to either 1T-phase MoS2 or the edges of 2H-phase MoS2, and the chemistry of covalent functionalization on the basal plane of 2H-MoS2 is poorly understood. Here, we report a facile approach to covalently functionalize chemical vapor deposition (CVD) grown 2H-MoS2 monolayers (MLs), as well as mechanically exfoliated MoS2, via thiol conjugation at sulfur vacancies on the basal plane. Thorough characterization confirmed the functionalization by thiol molecules on MoS2 MLs, and we experimentally proved that sulfur vacancies in MoS2 MLs play a key role in the functionalization of basal planes. By the controlling of the amount of sulfur vacancies via sulfur annealing, the degree of MoS2 functionalization was effectively tuned. Because thiol conjugation partially repairs or passivates sulfur vacancies, enhanced photoluminescence response and decreased active sites for hydrogen evolution catalysis were observed for functionalized MoS2. Moreover, such functionalization can be utilized for making MoS2-based heterostructures, an example of which was demonstrated using a dithiol molecule to link MoS2 layers and PbSe quantum dots. These results provide new understanding and insights on the surface chemistry of MoS2 and open up more opportunities for MoS2 MLs with well-controlled properties and broader applications.

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.