Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Direct patterning single-layer CVD graphene by oxidation scanning probe lithography.

Created on 11 Nov 2026

Authors

Jun Li, Hao Jia, Zekai Li, Jingjing Yang, Kaimin Luo, Jixiang Li, Xia Liu, Yeliang Wang, Min Tu, Pengcheng Xu, Xinxin Li

Published in

Nanoscale. Nov 10, 2026. Epub Nov 10, 2026.

Abstract

Single-layer graphene, with its atomic thickness and exceptional properties, offers great opportunities for high-performance nanoscale devices. While patterning is essential for translating the unique properties of graphene into functional devices, conventional ultraviolet (UV) lithography and electron-beam lithography (EBL) are constrained by limited resolution, resist residues and crystal damage. Here, we report nanoscale patterning of single-layer chemical vapor deposition (CVD) graphene using high-resolution, resist-free oxidation scanning probe lithography (o-SPL). By applying an alternating voltage to an electrically conductive probe, we demonstrate maskless, direct writing of graphene nanostructures on insulating substrates through the electrochemical reaction of graphene with water molecules. The dimensions of the patterned structures can be controlled by the voltage amplitude and probe scanning velocity, enabling single-layer graphene nanoribbons with widths down to ∼10 nm. This work highlights o-SPL as a precise and clean approach for patterning two-dimensional materials and functional devices.

PMID:
43007893
Bibliographic data and abstract were imported from PubMed on 11 Nov 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 5
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement