4.8 Article

A facile mechanochemical route to a covalently bonded graphitic carbon nitride (g-C3N4) and fullerene hybrid toward enhanced visible light photocatalytic hydrogen production

Journal

NANOSCALE
Volume 9, Issue 17, Pages 5615-5623

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7nr01237c

Keywords

-

Funding

  1. National Natural Science Foundation of China [21371164, 51572254]
  2. Fundamental Research Funds for the Central Universities [WK3430000002]

Ask authors/readers for more resources

Graphitic carbon nitride (g-C3N4) as an emerging two-dimensional (2D) nanomaterial has been commonly used as a metal-free photocatalyst with potential applications in visible light photocatalytic water-splitting. However, the photocatalytic activity of g-C3N4 is quite low due to its relatively large band gap and the existence of contact resistance between the nanosheets. Herein we report for the first time the facile synthesis of a covalently bonded g-C3N4/C-60 hybrid via a solid-state mechanochemical route and its application in photocatalytic hydrogen production under visible light. The g-C3N4/C-60 hybrid was synthesized by ball-milling g-C3N4 and C-60 in the presence of lithium hydroxide (LiOH) as a catalyst. The hybrid nature and conformation of the g-C3N4/C-60 hybrid were confirmed by a series of spectroscopic and morphological studies, featuring the covalent bonding of C-60 onto the edges of g-C3N4 nanosheets via a four-membered ring of azetidine, which has never been reported in fullerene chemistry. The g-C3N4/C-60 hybrid was further applied to metal-free visible light photocatalytic hydrogen production, affording a H-2 production rate of 266 mu mol h(-1) g(-1) without using any noble metal cocatalyst such as Pt, which is about 4.0 times higher than that obtained for the pristine g-C3N4 photocatalyst.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available