Abstract

AbstractMechanical dry transfer of large‐area graphene is increasingly applied in fabrication of graphene‐based electronic devices, and adhesion energy of graphene/substrate interface is a key factor affecting reliability and performance of these devices. Herein, the adhesion energy of a graphene/poly(ethylene terephthalate) (PET) interface is measured by widely adopted double cantilever beam (DCB) fracture tests. Results show that the apparent adhesion energy of sandwiched interface is highly rate‐dependent. When separation rate increases from 20 to 150 µm s−1, apparent adhesion energy increases by an order of magnitude. By examining fractured interfaces after DCB tests with micro‐Raman spectroscopy, the graphene is found to be fractured and transferred in fragments, with residual tensile strain up to 3% for high separation rates. The results are contrary to earlier reports, where higher separation rate in dry‐transfer process would typically enhance the dry transfer of graphene, resulting in better integrity and performance. Based on Raman spectroscopy measurements, three distinct decohesion modes are identified for PET‐/graphene‐/adhesive‐sandwiched interface, which consistently explain the rate‐dependent apparent adhesion energy. The complicated decohesion modes also suggest that an optimal separation rate should be used to properly measure the adhesion energy and improve the dry‐transfer technique of graphene with minimum damage and residual strain.

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.