Adsorption-Induced Expansion of Graphene Oxide Frameworks: Observation by in Situ Neutron Diffraction
Author(s) -
Joseph Schaeperkoetter,
Matthew Connolly,
Zachary Buck,
H. Taub,
H. Kaiser,
Carlos Wexler
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b02589
Subject(s) - neutron diffraction , supercritical fluid , graphene , materials science , adsorption , oxide , xenon , bar (unit) , graphite oxide , diffraction , graphite , hydrogen , methane , volume expansion , deformation (meteorology) , composite material , thermodynamics , chemistry , nanotechnology , optics , organic chemistry , physics , meteorology , metallurgy , medicine
We have investigated adsorption-induced deformation in graphene oxide framework materials (GOFs) using neutron diffraction at sample pressures up to 140 bar. GOFs, made by the solvothermal reaction of graphite oxide and benzene-1,4-diboronic acid, are a suitable candidate for deformation studies due to their narrow (∼1 nm), monodispersed, slit-shaped pores whose width can be measured by diffraction techniques. We have observed, in situ, a monotonic expansion of the slit width with increasing pressure upon adsorption of xenon, methane, and hydrogen under supercritical conditions. The expansion of ∼4% observed for xenon at a pressure of 48 bar is the largest deformation yet reported for supercritical adsorption on a carbonaceous material. We find that the expansion of the three gases can be mapped onto a common curve based solely on their Lennard-Jones parameters, in a manner similar to a law of corresponding states.
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