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dc.contributor.authorTang, J.
dc.contributor.authorSalunkhe, R.
dc.contributor.authorLiu, Jian
dc.contributor.authorTorad, N.
dc.contributor.authorImura, M.
dc.contributor.authorFurukawa, S.
dc.contributor.authorYamauchi, Y.
dc.date.accessioned2017-01-30T10:44:39Z
dc.date.available2017-01-30T10:44:39Z
dc.date.created2015-07-16T06:21:59Z
dc.date.issued2015
dc.identifier.citationTang, J. and Salunkhe, R. and Liu, J. and Yamauchi, Y. 2015. Thermal Conversion of Core-Shell Metal-Organic Frameworks: A New Method for Selectively Functionalized Nanoporous Hybrid Carbon. Journal of the American Chemical Society. 137: pp. 1572-1580.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/5223
dc.identifier.doi10.1021/ja511539a
dc.description.abstract

Core–shell structured ZIF-8@ZIF-67 crystals are well-designed and prepared through a seed-mediated growth method. After thermal treatment of ZIF-8@ZIF-67 crystals, we obtain selectively functionalized nanoporous hybrid carbon materials consisting of nitrogen-doped carbon (NC) as the cores and highly graphitic carbon (GC) as the shells. This is the first example of the integration of NC and GC in one particle at the nanometer level. Electrochemical data strongly demonstrate that this nanoporous hybrid carbon material integrates the advantageous properties of the individual NC and GC, exhibiting a distinguished specific capacitance (270 F·g–1) calculated from the galvanostatic charge–discharge curves at a current density of 2 A·g–1. Our study not only bridges diverse carbon-based materials with infinite metal–organic frameworks but also opens a new avenue for artificially designed nanoarchitectures with target functionalities.

dc.publisherAmerican Chemical Society
dc.titleThermal Conversion of Core-Shell Metal-Organic Frameworks: A New Method for Selectively Functionalized Nanoporous Hybrid Carbon
dc.typeJournal Article
dcterms.source.volume137
dcterms.source.startPage1572
dcterms.source.endPage1580
dcterms.source.issn0002-7863
dcterms.source.titleJournal of the American Chemical Society
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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