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Graphene induced porphyrin nano-aggregates for efficient electron transfer and photocurrent generation
- Source :
- Journal of Materials Chemistry C. 4:6027-6036
- Publication Year :
- 2016
- Publisher :
- Royal Society of Chemistry (RSC), 2016.
-
Abstract
- Significant research attention has been given to graphene–porphyrin hybrid materials for light harvesting. In this report, we demonstrate the influence of graphene surface and aging time on the formation of porphyrin [5-(4-hydroxyphenyl)-10,15,20-triphenyl porphyrin (4-HPTP)] aggregates. The large sp2 conjugated network of reduced graphene oxide (RGO) may facilitate strong π–π stacking interactions that influence the aggregation of 4-HPTP. The morphologies of these assembled structures are characterized by field emission scanning electron microscopy (FE-SEM). Steady state and time resolved spectroscopic studies reveal that the formation of J-type aggregation of 4-HPTP on an RGO surface is higher than on a graphene oxide (GO) surface. In situ growth of porphyrin nanoassemblies on an RGO surface improves the electronic interaction by shortening the interfacial distance between graphene and porphyrin. It is evident that the electron transfer process is enhanced in the presence of RGO upon the photoexcitation of porphyrin nanoassemblies which eventually generate a photocurrent. These graphene decorated porphyrin nanoassemblies are promising materials for the development of new generation optoelectronic devices.
- Subjects :
- Photocurrent
Materials science
Graphene
Stacking
Oxide
Nanotechnology
02 engineering and technology
General Chemistry
Conjugated system
010402 general chemistry
021001 nanoscience & nanotechnology
Photochemistry
01 natural sciences
Porphyrin
0104 chemical sciences
law.invention
Photoexcitation
Electron transfer
chemistry.chemical_compound
chemistry
law
Materials Chemistry
0210 nano-technology
Subjects
Details
- ISSN :
- 20507534 and 20507526
- Volume :
- 4
- Database :
- OpenAIRE
- Journal :
- Journal of Materials Chemistry C
- Accession number :
- edsair.doi...........8cf184f025c628d9857004b1a13d34d4