Abstract
As an effort to prepare carbon nanosheet and carbon film through catalyst- and transfer free process, several research groups have reported carbonization of polymers and small molecules such as polyacrylonitrile (PAN) and a small molecular pitch extracted from petroleum. Carbon nanosheets converted from PAN or pitch were obtained through two steps: cyclization and carbonization. Because the quality of the carbon materials sensitively depends on the cyclization conditions such as temperature, ramping rate, and oxygen contents, there is a great need for a cyclization-free process. Recently, we developed a cyclization-free carbonization process (one-step process) using PIM-1 (polymer of intrinsic microporosity). Various nano-structured PIM-1s were formed by using different methods such as electrospray, ultrasonic spray pyrolysis(USP), electrospining and spin coating methods, which were carbonized at 800~1200 oC without any catalyst. All carbonized PIM-1 maintained their original shape and their Raman spectra showed G graphitic carbon peak at 1590 cm-1 and D disordered carbon peak at 1330 cm-1. Especially, it is confirmed that carbonized PIM-1 prepared by spin coating had properties similar to graphene and could be used as the electrodes of ITO-free OSCs. Carbon nanosheets converted from PIM-1 showed a high efficiency of 1.922 % and electrical conductivity of 500 S/cm. In this presentation, shape and dimension control of carbon materials and direct use as electrodes of organic solar cells and supercapacitors will be discussed more in detail.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.