CVD grown nitrogen doped graphene is an exceptional visible-light driven photocatalyst for surface catalytic reactions
Creators
- 1. Department of Electrical and Computer Engineering, University of Alberta, 9211-116 St., Edmonton, AB T6G 1H9 (Canada)
- 2. Engineering Research Center for Nanophotonics and Advanced Instrument, School of Physics and Electronic Science, East China Normal University, Shanghai 200062 (China)
- 3. Nanotechnology Research Centre, National Research Council Canada, 11421 Saskatchewan Drive, Edmonton, AB T6G 2M9 (Canada)
Description
The photocatalytic potential of large area CVD grown nitrogen doped graphene (NGr) has been explored though the chemical transformation of 4-nitrobenzene thiol into p,p′-dimercaptoazobenzene. Decoration of NGr with Ag nanocubes with rounded edges to form NGr/Ag nanohybrids resulted in a slight increase in the work-function and a decrease in the n-type character of NGr due to ground state transfer of negative charge from NGr to Ag. The Ag nanocubes exhibited a localized surface plasmon resonance (LSPR) at ~425 nm. When the NGr/Ag nanohybrids were illuminated with visible light of wavelength close to the LSPR peak, Kelvin probe force microscopy (KPFM) indicated a dramatic change in surface potential of −225 mV and Raman spectra detected electron accumulation in NGr, which are attributed to a high local field enhancement-mediated hot electron injection into NGr and the formation of long-lived charge separated states. Pristine nitrogen doped graphene and its coupled system with plasmonic Ag nanoparticles showed superior photocatalytic performance compared to bare plasmonic Ag catalyst. While standalone Ag NPs were unable to complete the transformation of 4-NBT into DMAB even at a laser power of 10 mW, NGr/Ag nanohybrids completed this transformation at a laser power of 1 mW, pointing to the high photoreduction strength of NGr/Ag. Density functional theory (DFT) based computational modeling was used to examine the electronic structure of graphene doped with graphitic, pyridinic and pyrrolic nitrogen dopant atoms. DFT results indicated an enhanced chemical reactivity of NGr due to stronger localization of charge at the dopant sites and a pronounced difference in the projected density of states (PDOS) for carbon atoms in proximity to, and distant from, the nitrogen dopant sites. (paper)
Availability note (English)
Available from http://dx.doi.org/10.1088/2053-1583/ab4554Additional details
Identifiers
Publishing Information
- Journal Title
- 2D Materials
- Journal Volume
- 7
- Journal Issue
- 1
- Journal Page Range
- [19 p.]
- ISSN
- 2053-1583
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 52060712
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- CHEMICAL VAPOR DEPOSITION; DENSITY FUNCTIONAL METHOD; DENSITY OF STATES; DOPED MATERIALS; ELECTRON BEAM INJECTION; GRAPHENE; GRAPHITE; GROUND STATES; LASERS; NANOPARTICLES; NITROBENZENE; PHOTOCATALYSIS; PLASMONS; RAMAN SPECTRA; SURFACE POTENTIAL; SURFACES; THIOLS
- Descriptors DEC
- BEAM INJECTION; CALCULATION METHODS; CARBON; CATALYSIS; CHEMICAL COATING; DEPOSITION; ELEMENTS; ENERGY LEVELS; MATERIALS; MINERALS; NITRO COMPOUNDS; NONMETALS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; PARTICLES; POTENTIALS; QUASI PARTICLES; SPECTRA; SURFACE COATING; VARIATIONAL METHODS