4.8 Article

Electrospun Composite Nanofiber Yarns Containing Oriented Graphene Nanoribbons

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 5, 期 13, 页码 6225-6231

出版社

AMER CHEMICAL SOC
DOI: 10.1021/am401161b

关键词

graphene nanoribbon; nanocomposite; nanofiber; electrospinning; mechanical properties; electrical properties

资金

  1. International Technology Center-Pacific (ITC-PAC)
  2. U.S. Army Research Development and Engineering Command (RDECOM)
  3. U.S. Army Natic Soldier Center
  4. Japan Society for Promotion of Science, JSPS [239234]
  5. AFOSR [FA9550-09-1-0581]
  6. AFOSR through the University Technology Corporation [09-S568-064-01-C1]
  7. AFOSR MURI [FA9550-12-1-00350]

向作者/读者索取更多资源

The graphene nanoribbon (GNR)/carbon composite nanofiber yarns were prepared by electrospinning from poly(acrylonitrile) (PAN) containing graphene oxide nanoribbons (GONRs), and successive twisting and carbonization. The electrospinning process can exert directional shear force coupling with the external electric field to the flow of the spinning solution. During electrospinning, the well-dispersed GONRs were highly oriented along the fiber axis in an electrified thin liquid jet. The addition of GONRs at a low weight fraction significantly improved the mechanical properties of the composite nanofiber yarns. In addition, the carbonization of the matrix polymer enhanced not only the mechanical but also the electrical properties of the composites. The electrical conductivity of the carbonized composite yarns containing 0.5 wt% GONR showed the maximum value of 165 S cm(-1). It is larger than the maximum value of the reported electrospun carbon composite yarns. Interestingly, it is higher than the conductivities of both the PAN-based pristine CNF yarns (77 S cm(-1)) and the monolayer GNRs (54 S cm(-1)). These results and Raman spectroscopy supported the hypothesis that the oriented GONRs contained in the PAN nanofibers effectively functioned as not only the 1-D nanofiller but also the nanoplatelet promoter of stabilization and template agent for the carbonization.

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