Please use this identifier to cite or link to this item: https://doi.org/10.1038/ncomms2579
DC FieldValue
dc.titleA hydrothermal anvil made of graphene nanobubbles on diamond
dc.contributor.authorXuan Lim, C.H.Y.
dc.contributor.authorSorkin, A.
dc.contributor.authorBao, Q.
dc.contributor.authorLi, A.
dc.contributor.authorZhang, K.
dc.contributor.authorNesladek, M.
dc.contributor.authorLoh, K.P.
dc.date.accessioned2014-06-23T05:30:22Z
dc.date.available2014-06-23T05:30:22Z
dc.date.issued2013
dc.identifier.citationXuan Lim, C.H.Y., Sorkin, A., Bao, Q., Li, A., Zhang, K., Nesladek, M., Loh, K.P. (2013). A hydrothermal anvil made of graphene nanobubbles on diamond. Nature Communications 4 : -. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms2579
dc.identifier.issn20411723
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75439
dc.description.abstractThe hardness and virtual incompressibility of diamond allow it to be used in high-pressure anvil cell. Here we report a new way to generate static pressure by encapsulating single-crystal diamond with graphene membrane, the latter is well known for its superior nano-indentation strength and in-plane rigidity. Heating the diamond-graphene interface to the reconstruction temperature of diamond (∼1,275 K) produces a high density of graphene nanobubbles that can trap water. At high temperature, chemical bonding between graphene and diamond is robust enough to allow the hybrid interface to act as a hydrothermal anvil cell due to the impermeability of graphene. Superheated water trapped within the pressurized graphene nanobubbles is observed to etch the diamond surface to produce a high density of square-shaped voids. The molecular structure of superheated water trapped in the bubble is probed using vibrational spectroscopy and dynamic changes in the hydrogen-bonding environment are observed. © 2013 Macmillan Publishers Limited. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1038/ncomms2579
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1038/ncomms2579
dc.description.sourcetitleNature Communications
dc.description.volume4
dc.description.page-
dc.identifier.isiut000318873900010
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