The Route to Functional Graphene Oxide

被引:309
作者
Haubner, Kinga
Murawski, Jan [1 ]
Olk, Phillip [1 ]
Eng, Lukas M. [1 ]
Ziegler, Christoph
Adolphi, Barbara [2 ]
Jaehne, Evelin [1 ]
机构
[1] Tech Univ Dresden, Inst Angew Photophys, D-01069 Dresden, Germany
[2] Tech Univ Dresden, Inst Halbleiter & Syst Tech, D-01069 Dresden, Germany
关键词
carbon; dyes/pigments; graphene oxide; oxidation; reduction; METHYLENE-BLUE; GRAPHITE OXIDE; SURFACE MODIFICATION; EXFOLIATED GRAPHITE; CHEMICAL-REDUCTION; AQUEOUS SUSPENSION; AMORPHOUS-CARBON; SHEETS; FILMS; WATER;
D O I
10.1002/cphc.201000132
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report on an easy-to-use, successful, and reproducible route to synthesize functionalized graphite oxide (GO) and its conversion to graphene-like materials through chemical or thermal reduction of GO. Graphite oxide containing hydroxyl, epoxy, carbonyl, and carboxyl groups loses mainly hydroxyl and epoxy groups during reduction, whereas carboxyl species remain untouched. The interaction of functionalized graphene with fluorescent methylene blue (MB) is investigated and compared to graphite, fully oxidized GO, as well as thermally and chemically reduced GO. Optical absorption and emission spectra of the composites indicate a clear preference for MB interaction with the GO derivatives containing a large number of functional groups (GO and chemically reduced GO), whereas graphite and thermally reduced GO only incorporate a few MB molecules. These findings are consistent with thermogravimetric, X-ray photoelectron spectroscopic, and Raman data recorded at every stage of preparation. The optical data also indicate concentration-dependent aggregation of MB on the GO surface leading to stable MB dimers and trimers. The MB dimers are responsible for fluorescence quenching, which can be controlled by varying the pH value.
引用
收藏
页码:2131 / 2139
页数:9
相关论文
共 52 条
[1]   Chemical Modification of Epitaxial Graphene: Spontaneous Grafting of Aryl Groups [J].
Bekyarova, Elena ;
Itkis, Mikhail E. ;
Ramesh, Palanisamy ;
Berger, Claire ;
Sprinkle, Michael ;
de Heer, Walt A. ;
Haddon, Robert C. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (04) :1336-+
[2]   A SPECTROSCOPIC STUDY OF METHYLENE BLUE MONOMER, DIMER, AND COMPLEXES WITH MONTMORILLONITE [J].
BERGMANN, K ;
OKONSKI, CT .
JOURNAL OF PHYSICAL CHEMISTRY, 1963, 67 (10) :2169-&
[3]   DAS ADSORPTIONSVERHALTEN SEHR DUNNER KOHLENSTOFF-FOLIEN [J].
BOEHM, HP ;
CLAUSS, A ;
FISCHER, GO ;
HOFMANN, U .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1962, 316 (3-4) :119-127
[4]   SOME ASPECTS OF THE SURFACE-CHEMISTRY OF CARBON-BLACKS AND OTHER CARBONS [J].
BOEHM, HP .
CARBON, 1994, 32 (05) :759-769
[5]   Graphite oxide:: Chemical reduction to graphite and surface modification with primary aliphatic amines and amino acids [J].
Bourlinos, AB ;
Gournis, D ;
Petridis, D ;
Szabó, T ;
Szeri, A ;
Dékány, I .
LANGMUIR, 2003, 19 (15) :6050-6055
[6]   EVIDENCE FOR TRIMERIZATION IN AQUEOUS SOLUTIONS OF METHYLENE BLUE [J].
BRASWELL, E .
JOURNAL OF PHYSICAL CHEMISTRY, 1968, 72 (07) :2477-&
[7]  
Brodie B. C., 1860, ANN CHIM PHYS, V59, P466
[8]   Structure of cationic dyes assemblies intercalated in the films of montmorillonite [J].
Bujdak, Juraj ;
Czimerova, Adriana ;
Iyi, Nobuo .
THIN SOLID FILMS, 2008, 517 (02) :793-799
[9]  
Cassagneau T, 1998, ADV MATER, V10, P877, DOI 10.1002/(SICI)1521-4095(199808)10:11<877::AID-ADMA877>3.0.CO
[10]  
2-1