In Situ Nucleation‐Decoupled and Site‐Specific Incorporation of Å‐Scale Pores in Graphene Via Epoxidation. Issue 51 (18th November 2022)

• Record Type: Journal Article
• Authors: Huang, Shiqi; Villalobos, Luis Francisco; Li, Shaoxian; Vahdat, Mohammad Tohidi; Chi, Heng‐Yu; Hsu, Kuang‐Jung; Bondaz, Luc; Boureau, Victor; Marzari, Nicola; Agrawal, Kumar Varoon
• Is Part Of: Advanced materials. Volume 34:Issue 51(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-11-18
• Subjects: Å‐scale pore manipulation -- epoxidation -- etching kinetics -- graphene nanopore -- in situ gasification; Materials -- Periodicals; Chemical vapor deposition -- Periodicals; 620.11
• DOI: 10.1002/adma.202206627
• Languages: English
• ISSNs: 0935-9648

Abstract

Abstract: Generating pores in graphene by decoupled nucleation and expansion is desired to achieve a fine control over the porosity, and is desired to advance several applications. Herein, epoxidation is introduced, which is the formation of nanosized epoxy clusters on the graphitic lattice as nucleation sites without forming pores. In situ gasification of clusters inside a transmission electron microscope shows that pores are generated precisely at the site of the clusters by surpassing an energy barrier of 1.3 eV. Binding energy predictions using ab initio calculations combined with the cluster nucleation theory reveal the structure of the epoxy clusters and indicate that the critical cluster is an epoxy dimer. Finally, it is shown that the cluster gasification can be manipulated to form Å‐scale pores which then effectively sieve gas molecules based on their size. This decoupled cluster nucleation and pore formation will likely pave the way for an independent control of pore size and density. Abstract : Nanosized epoxy clusters form on graphene surface upon exposure to ozone near room temperature. When sufficient energy is supplied, clusters gasify forming nanopores. The energy barrier is measured for cluster formation as 0.42 eV and for cluster gasification in the pore as 1.3 eV. The approach allows decoupling of pore nucleation (pore density) and expansion (pore size).