메뉴 건너뛰기




Volumn 4, Issue , 2013, Pages

Atomically precise edge chlorination of nanographenes and its application in graphene nanoribbons

Author keywords

[No Author keywords available]

Indexed keywords

GRAPHENE; GRAPHENE NANORIBBON; NANOGRAPHENE; NANORIBBON; UNCLASSIFIED DRUG;

EID: 84887645907     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms3646     Document Type: Article
Times cited : (184)

References (36)
  • 2
    • 67649225738 scopus 로고    scopus 로고
    • Graphene: Status and prospects
    • Geim, A. K. Graphene: status and prospects. Science 324, 1530-1534 (2009).
    • (2009) Science , vol.324 , pp. 1530-1534
    • Geim, A.K.1
  • 4
    • 60949104104 scopus 로고    scopus 로고
    • The influence of edge structure on the electronic properties of graphene quantum dots and nanoribbons
    • Ritter, K. A. & Lyding, J. W. The influence of edge structure on the electronic properties of graphene quantum dots and nanoribbons. Nat. Mater. 8, 235-242 (2009).
    • (2009) Nat. Mater. , vol.8 , pp. 235-242
    • Ritter, K.A.1    Lyding, J.W.2
  • 5
    • 84883225909 scopus 로고    scopus 로고
    • Nanographene and graphene edges: Electronic structure and nanofabrication
    • Fujii, S. & Enoki, T. Nanographene and graphene edges: electronic structure and nanofabrication. Acc. Chem. Res. 46, 2202-2210 (2012).
    • (2012) Acc. Chem. Res. , vol.46 , pp. 2202-2210
    • Fujii, S.1    Enoki, T.2
  • 6
    • 82955190404 scopus 로고    scopus 로고
    • Chemistry and physics of a single atomic layer: Strategies and challenges for functionalization of graphene and graphene-based materials
    • Yan, L. et al. Chemistry and physics of a single atomic layer: strategies and challenges for functionalization of graphene and graphene-based materials. Chem. Soc. Rev. 41, 97-114 (2012).
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 97-114
    • Yan, L.1
  • 7
    • 84869194037 scopus 로고    scopus 로고
    • Functionalization of graphene: Covalent and non-covalent approaches, derivatives and applications
    • Georgakilas, V. et al. Functionalization of graphene: covalent and non-covalent approaches, derivatives and applications. Chem. Rev. 112, 6156-6214 (2012).
    • (2012) Chem. Rev. , vol.112 , pp. 6156-6214
    • Georgakilas, V.1
  • 8
    • 84872713615 scopus 로고    scopus 로고
    • Effect of covalent chemistry on the electronic structure and properties of carbon nanotubes and graphene
    • Bekyarova, E. et al. Effect of covalent chemistry on the electronic structure and properties of carbon nanotubes and graphene. Acc. Chem. Res 46, 65-76 (2013).
    • (2013) Acc. Chem. Res , vol.46 , pp. 65-76
    • Bekyarova, E.1
  • 9
    • 34547380841 scopus 로고    scopus 로고
    • Intrinsic current-voltage characteristics of graphene nanoribbon transistors and effect of edge doping
    • DOI 10.1021/nl070133j
    • Yan, Q. et al. Intrinsic current-voltage characteristics of graphene nanoribbon transistors and effect of edge doping. Nano Lett. 7, 1469-1473 (2007). (Pubitemid 47140408)
    • (2007) Nano Letters , vol.7 , Issue.6 , pp. 1469-1473
    • Yan, Q.1    Huang, B.2    Yu, J.3    Zheng, F.4    Zang, J.5    Wu, J.6    Gu, B.-L.7    Liu, F.8    Duan, W.9
  • 10
    • 34548146633 scopus 로고    scopus 로고
    • Enhanced half-metallicity in edge-oxidized zigzag graphene nanoribbons
    • DOI 10.1021/nl0708922
    • Hod, O., Barone, V., Peralta, J. E. & Scuseria, G. E. Enhanced half-metallicity in edge-oxidized zigzag graphene nanoribbons. Nano Lett. 7, 2295-2299 (2007). (Pubitemid 47310122)
    • (2007) Nano Letters , vol.7 , Issue.8 , pp. 2295-2299
    • Hod, O.1    Barone, V.2    Peralta, J.E.3    Scuseria, G.E.4
  • 12
    • 82655168279 scopus 로고    scopus 로고
    • Ab initio calculations of edge-functionalized armchair graphene nanoribbons: Structural, electronic, and vibrational effects
    • Rosenkranz, N., Till, C., Thomsen, C. & Maultzsch, J. Ab initio calculations of edge-functionalized armchair graphene nanoribbons: Structural, electronic, and vibrational effects. Phys. Rev. B 84, 195438 (2011).
    • (2011) Phys. Rev. B , vol.84 , pp. 195438
    • Rosenkranz, N.1    Till, C.2    Thomsen, C.3    Maultzsch, J.4
  • 13
    • 66249123595 scopus 로고    scopus 로고
    • N-doping of graphene through electrothermal reactions with ammonia
    • Wang, X. et al. N-doping of graphene through electrothermal reactions with ammonia. Science 324, 768-771 (2009).
    • (2009) Science , vol.324 , pp. 768-771
    • Wang, X.1
  • 14
    • 79959776290 scopus 로고    scopus 로고
    • Large-area graphene films by simple solution casting of edgeselectively functionalized graphite
    • Bae, S.-Y. et al. Large-area graphene films by simple solution casting of edgeselectively functionalized graphite. ACS Nano 5, 4974-4980 (2011).
    • (2011) ACS Nano , vol.5 , pp. 4974-4980
    • Bae, S.-Y.1
  • 15
    • 80052437337 scopus 로고    scopus 로고
    • Formation of large-area nitrogen-doped graphene film prepared from simple solution casting of edge-selectively functionalized graphite and its electrocatalytic activity
    • Jeon, I. Y. et al. Formation of large-area nitrogen-doped graphene film prepared from simple solution casting of edge-selectively functionalized graphite and its electrocatalytic activity. Chem. Mater. 23, 3987-3992 (2011).
    • (2011) Chem. Mater. , vol.23 , pp. 3987-3992
    • Jeon, I.Y.1
  • 16
    • 84859620458 scopus 로고    scopus 로고
    • Edge-carboxylated graphene nanosheets via ball milling
    • Jeon, I. Y. et al. Edge-carboxylated graphene nanosheets via ball milling. Proc. Natl Acad. Sci. USA 109, 5588-5593 (2012).
    • (2012) Proc. Natl Acad. Sci. USA , vol.109 , pp. 5588-5593
    • Jeon, I.Y.1
  • 17
    • 33947712905 scopus 로고    scopus 로고
    • Graphenes as potential material for electronics
    • DOI 10.1021/cr068010r
    • Wu, J., Pisula, W. & Mullen, K. Graphenes as potential material for electronics. Chem. Rev. 107, 718-747 (2007). (Pubitemid 46504818)
    • (2007) Chemical Reviews , vol.107 , Issue.3 , pp. 718-747
    • Wu, J.1    Pisula, W.2    Mullen, K.3
  • 18
    • 79961050052 scopus 로고    scopus 로고
    • Photochemical chlorination of graphene
    • Li, B. et al. Photochemical chlorination of graphene. ACS Nano 5, 5957-5961 (2011).
    • (2011) ACS Nano , vol.5 , pp. 5957-5961
    • Li, B.1
  • 19
    • 83055165802 scopus 로고    scopus 로고
    • Controlled chlorine plasma reaction for noninvasive graphene doping
    • Wu, J. et al. Controlled chlorine plasma reaction for noninvasive graphene doping. J. Am. Chem. Soc. 133, 19668-19671 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 19668-19671
    • Wu, J.1
  • 20
    • 84866985559 scopus 로고    scopus 로고
    • Production of graphite chloride and bromide using microwave sparks
    • Zheng, J. et al. Production of graphite chloride and bromide using microwave sparks. Sci. Rep. 2, 662 (2012).
    • (2012) Sci. Rep. , vol.2 , pp. 662
    • Zheng, J.1
  • 21
    • 53549115949 scopus 로고    scopus 로고
    • 18,18 '-dihexyl 9,9' biphenanthro 9,10-b triphenylene: Construction and consequences of a profoundly hindered aryl-aryl single bond
    • Hilton, C. L., Crowfoot, J. M., Rempala, P. & King, B. T. 18,18 '-dihexyl 9,9' biphenanthro 9,10-b triphenylene: construction and consequences of a profoundly hindered aryl-aryl single bond. J. Am. Chem. Soc. 130, 13392-13399 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 13392-13399
    • Hilton, C.L.1    Crowfoot, J.M.2    Rempala, P.3    King, B.T.4
  • 22
    • 0002519894 scopus 로고
    • Crystallization of large planar polycyclic aromatic hydrocarbons: The molecular and crystal structures of hexabenzo[bc,ef,hi,kl,no,qr]coronene and benzo[1,2,3- bc:4,5,6-b0c0]dicoronene
    • Goddard, R., Haenel, M. W., Herndon, W. C., Krueger, C. & Zander, M. Crystallization of large planar polycyclic aromatic hydrocarbons: the molecular and crystal structures of hexabenzo[bc,ef,hi,kl,no,qr]coronene and benzo[1,2,3- bc:4,5,6-b0c0]dicoronene. J. Am. Chem. Soc. 117, 30-41 (1995).
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 30-41
    • Goddard, R.1    Haenel, M.W.2    Herndon, W.C.3    Krueger, C.4    Zander, M.5
  • 23
    • 84864199010 scopus 로고    scopus 로고
    • High quality dispersions of hexabenzocoronene in organic solvents
    • Hughes, J. M. et al. High quality dispersions of hexabenzocoronene in organic solvents. J. Am. Chem. Soc. 134, 12168-12179 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 12168-12179
    • Hughes, J.M.1
  • 25
    • 26544480072 scopus 로고
    • Total-energy all-electron density functional method for bulk solids and surfaces
    • Weinert, M., Wimmer, E. & Freeman, A. J. Total-energy all-electron density functional method for bulk solids and surfaces. Phys. Rev. B 26, 4571-4578 (1982).
    • (1982) Phys. Rev. B , vol.26 , pp. 4571-4578
    • Weinert, M.1    Wimmer, E.2    Freeman, A.J.3
  • 26
    • 0141789719 scopus 로고    scopus 로고
    • Aromaticity of polycyclic conjugated hydrocarbons
    • Randic, M. Aromaticity of polycyclic conjugated hydrocarbons. Chem. Rev. 103, 3449-3605 (2003).
    • (2003) Chem. Rev. , vol.103 , pp. 3449-3605
    • Randic, M.1
  • 27
    • 77949360616 scopus 로고    scopus 로고
    • Clar's theory, p-electron distribution, and geometry of graphene nanoribbons
    • Wassmann, T., Seitsonen, A. P., Saitta, A. M., Lazzeri, M. & Mauri, F. Clar's theory, p-electron distribution, and geometry of graphene nanoribbons. J. Am. Chem. Soc. 132, 3440-3451 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 3440-3451
    • Wassmann, T.1    Seitsonen, A.P.2    Saitta, A.M.3    Lazzeri, M.4    Mauri, F.5
  • 28
    • 62149090279 scopus 로고    scopus 로고
    • Geometry and bonding in the ground and lowest triplet state of D6h symmetric crenellated edged C6[3m(m1)1]H6(2m1) (m2, 6) graphene hydrocarbon molecules
    • Philpott, M. R. & Kawazoe, Y. Geometry and bonding in the ground and lowest triplet state of D6h symmetric crenellated edged C6[3m(m1)1]H6(2m1) (m2, 6) graphene hydrocarbon molecules. Chem. Phys. 358, 85-95 (2009).
    • (2009) Chem. Phys. , vol.358 , pp. 85-95
    • Philpott, M.R.1    Kawazoe, Y.2
  • 29
    • 0000878272 scopus 로고
    • The crystal and molecular structure of corannulene, C20H10
    • Hanson J. C. & Nordman, C. E. The crystal and molecular structure of corannulene, C20H10. Acta Crystallogr. Sect. B B32, 1147-1153 1976
    • (1976) Acta Crystallogr. Sect. B , vol.B32 , pp. 1147-1153
    • Hanson, J.C.1    Nordman, C.E.2
  • 30
    • 36849056919 scopus 로고
    • Crystal structures of polynuclear aromatic hydrocarbons: Classification, rationalization and prediction from molecular structure
    • Desiraju, G. R. & Gavezzotti, A. Crystal structures of polynuclear aromatic hydrocarbons: classification, rationalization and prediction from molecular structure. Acta Crystallogr. Sect. B B45, 473-482 (1989).
    • (1989) Acta Crystallogr. Sect. B , vol.B45 , pp. 473-482
    • Desiraju, G.R.1    Gavezzotti, A.2
  • 31
    • 77950874284 scopus 로고    scopus 로고
    • Forever young: Polycyclic aromatic hydrocarbons as model cases for structural and optical studies
    • Rieger, R. & Mullen, K. Forever young: polycyclic aromatic hydrocarbons as model cases for structural and optical studies. J. Phys. Org. Chem. 23, 315-325 (2010).
    • (2010) J. Phys. Org. Chem. , vol.23 , pp. 315-325
    • Rieger, R.1    Mullen, K.2
  • 32
    • 8544228377 scopus 로고    scopus 로고
    • Introduction to organic thin film transistors and design of n-channel organic semiconductors
    • Newman, C. R. et al. Introduction to organic thin film transistors and design of n-channel organic semiconductors. Chem. Mater. 16, 4436-4451 (2004).
    • (2004) Chem. Mater. , vol.16 , pp. 4436-4451
    • Newman, C.R.1
  • 35
    • 0037799714 scopus 로고    scopus 로고
    • Hybrid functionals based on a screened Coulomb potential
    • Heyd, J., Scuseria, G. E. & Ernzerhof, M. Hybrid functionals based on a screened Coulomb potential. J. Chem. Phys. 118, 8207-8215 (2003).
    • (2003) J. Chem. Phys. , vol.118 , pp. 8207-8215
    • Heyd, J.1    Scuseria, G.E.2    Ernzerhof, M.3
  • 36
    • 0035879976 scopus 로고    scopus 로고
    • 6-31G basis set for third-Row atoms
    • DOI 10.1002/jcc.1058
    • Rassolov, V. A., Ratner, M. A., Pople, J. A., Redfern, P. C. & Curtiss, L. A. 6-31G basis set for third-row atoms. J. Comput. Chem. 22, 976-984 (2001). (Pubitemid 32455735)
    • (2001) Journal of Computational Chemistry , vol.22 , Issue.9 , pp. 976-984
    • Rassolov, V.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.