| Literature DB >> 32427466 |
Eoin Griffin1, Lucas Mogg1, Guang-Ping Hao1,2, Gopinadhan Kalon1,3, Cihan Bacaksiz4, Guillermo Lopez-Polin1,5, T Y Zhou6, Victor Guarochico1, Junhao Cai1, Christof Neumann7, Andreas Winter7, Michael Mohn8, Jong Hak Lee9, Junhao Lin10,11, Ute Kaiser8, Irina V Grigorieva1, Kazu Suenaga10, Barbaros Özyilmaz9, Hui-Min Cheng6,12, Wencai Ren6, Andrey Turchanin7, Francois M Peeters4, Andre K Geim1, Marcelo Lozada-Hidalgo1.
Abstract
Defect-free graphene is impermeable to gases and liquids but highly permeable to thermal protons. Atomic-scale defects such as vacancies, grain boundaries, and Stone-Wales defects are predicted to enhance graphene's proton permeability and may even allow small ions through, whereas larger species such as gas molecules should remain blocked. These expectations have so far remained untested in experiment. Here, we show that atomically thin carbon films with a high density of atomic-scale defects continue blocking all molecular transport, but their proton permeability becomes ∼1000 times higher than that of defect-free graphene. Lithium ions can also permeate through such disordered graphene. The enhanced proton and ion permeability is attributed to a high density of eight-carbon-atom rings. The latter pose approximately twice lower energy barriers for incoming protons compared to that of the six-atom rings of graphene and a relatively low barrier of ∼0.6 eV for Li ions. Our findings suggest that disordered graphene could be of interest as membranes and protective barriers in various Li-ion and hydrogen technologies.Entities:
Keywords: battery; disorder; fuel cell; graphene; lithium ion; proton
Year: 2020 PMID: 32427466 DOI: 10.1021/acsnano.0c02496
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881