TY - JOUR
T1 - Graphene oxide-iron complex
T2 - Synthesis, characterization and visible-light-driven photocatalysis
AU - Dong, Ying
AU - Li, Jing
AU - Shi, Lei
AU - Xu, Jun
AU - Wang, Xiaobo
AU - Guo, Zhiguang
AU - Liu, Weimin
PY - 2013/1/21
Y1 - 2013/1/21
N2 - Graphene as an important two-dimensional one-atom-thick nanosheet can be regarded as a solid and also a molecule. In this paper, we focused attention on the coordination ability of doping-induced defects, micro-scale size and atomic thickness of graphene, and anchored oxygen-donor coordination of graphene oxide to ferric ions, forming a giant flat iron complex. As well as graphene oxide, as-obtained graphene oxide-Fe(iii) complexes were characterized by transmission electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, and so on. It was demonstrated that graphene oxide-Fe(iii) complexes could be well dispersed in water, with size up to micrometers and atomically thin. Under visible-light irradiation, graphene oxide-Fe(iii) complexes displayed homogeneous catalytic ability of H2O2 activation, and could be easily removed by simple filtration or centrifugation, showing significant advantages in both homogeneous and heterogeneous catalysis.
AB - Graphene as an important two-dimensional one-atom-thick nanosheet can be regarded as a solid and also a molecule. In this paper, we focused attention on the coordination ability of doping-induced defects, micro-scale size and atomic thickness of graphene, and anchored oxygen-donor coordination of graphene oxide to ferric ions, forming a giant flat iron complex. As well as graphene oxide, as-obtained graphene oxide-Fe(iii) complexes were characterized by transmission electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, and so on. It was demonstrated that graphene oxide-Fe(iii) complexes could be well dispersed in water, with size up to micrometers and atomically thin. Under visible-light irradiation, graphene oxide-Fe(iii) complexes displayed homogeneous catalytic ability of H2O2 activation, and could be easily removed by simple filtration or centrifugation, showing significant advantages in both homogeneous and heterogeneous catalysis.
UR - http://www.scopus.com/inward/record.url?scp=84876557398&partnerID=8YFLogxK
U2 - 10.1039/c2ta00371f
DO - 10.1039/c2ta00371f
M3 - 文章
AN - SCOPUS:84876557398
SN - 2050-7488
VL - 1
SP - 644
EP - 650
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 3
ER -