Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. Packing efficiency and accessible surface area of crumpled graphene

Packing efficiency and accessible surface area of crumpled graphene

Thumbnail Image
Download
Name

Cranford-2011-Packing efficiency and accessible surface area.pdf

Size

813.75 KB

Format

Adobe PDF

Checksum (MD5)

431a0cc74efaf26c38a2b5299e63f1d0

Author(s)
Cranford, Steven
•
Buehler, Markus J
Date Issued
November 2011
Journal
Physical Review B
Publisher
American Physical Society
Citation
Cranford, Steven, and Markus Buehler. “Packing Efficiency and Accessible Surface Area of Crumpled Graphene.” Physical Review B 84.20 (2011): [7 pages].©2011 American Physical Society.
Version
Final published version
Abstract
Graphene holds promise as an ultracapacitor due to its high specific surface area and intrinsic capacitance. To exploit both, a maximum surface area must be accessible while the two-dimensional (2D) graphene is deformed to fill volume. Here, we study stable crumpled graphene sheets of different lengths, L, using full atomistic molecular dynamics (MD) and determine a fractal dimension of D≅2.36±0.12, indicating efficient spatial packing. Introduction of defects inducing a transition from membrane-like to amorphous carbon further enhances packing efficiency. Further, variation of self-adhesion energy indicates a predominant role in randomly folded graphene. We determine that approximately 60% of the specific surface area of graphene is solvent accessible once crumpled and can be tuned with applied compression and crumpling. We analyze the solvent accessible surface area (SASA) and approximate the upper bound of free crumpled graphene capacitance to ≈329 F/g. Once crumpled, the achievable capacitance is highly dependent on the confined volume.
MIT Department
Massachusetts Institute of Technology. Department of Civil and Environmental Engineering
Massachusetts Institute of Technology. Department of Materials Science and Engineering
Massachusetts Institute of Technology. Laboratory for Atomistic and Molecular Mechanics
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
http://hdl.handle.net/1721.1/70129
DOI of Published Version
https://doi.org/10.1103/PhysRevB.84.205451
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.