4.6 Article

Tunable Synthesis of Nitrogen Doped Graphene from Fluorographene under Mild Conditions

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 8, Issue 12, Pages 4764-4772

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.9b07161

Keywords

Nitrogen-doped graphene; Fluorographene; Wet chemistry; Eco-friendly organic synthesis; Density functional theory; Reaction mechanism

Funding

  1. MEYS [CZ.02.1.01/0.0/0.0/16_019/0000754, CZ.1.05/2.1.00/19.0377]
  2. ERC [683024]
  3. Internal Student Grant Agency of the Palacky University in Olomouc, Czech Republic [IGA_PrF_2019_031]

Ask authors/readers for more resources

The nitrogen doping of graphene via mild and low energy processes to afford homogeneous product composition and topology with high nitrogen content (>10 at. %) remains a challenge of contemporary 2D materials chemistry. Here, we report a previously unexplored route to synthesize N-doped graphene (NG) with exceptionally high N content (up to 18.2 at. %) by reaction of fluorographene (FG) with NaNH2 in N,N-dimethylformamide (at 130 degrees C) or acetonitrile (at 70 degrees C). The N content can be tuned by changing the reaction time, temperature, and/or solvent, ranging from 6.6 to 18.2 at. %, mainly in the form of pyridinic and pyrrolic configurations. With thermal annealing, the N content remained constant up to 400 degrees C but then decreased by similar to 50% upon being further annealed to 1000 degrees C. Density functional theory (DFT) calculations showed that nitrogen incorporation into the carbon lattice mostly occurred at vacancies present in the starting material. We also conducted a thorough rationalization of side-reaction pathways leading to byproducts, which were confirmed by GC-MS analysis. This is the highest yet recorded N content for a wet chemical doping procedure and at such a low temperature of 70 degrees C. The reported synthetic approach thus offers a sustainable and cost-effective way to prepare NG with a broad tunability window of N content for potential applications related to energy storage and catalysis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available