Loading…

Tailoring the Electronic Properties of Graphene Quantum Dots by P Doping and Their Enhanced Performance in Metal-Free Composite Photocatalyst

Graphene quantum dots (GQDs) as new 0-dimensional (0D) materials have exhibited promising applications in numerous fields, and these enormous potentials are largely dependent on their electronic properties. Herein we tailored the semiconductive behavior of GQDs and transformed the n-type hydrotherma...

Full description

Saved in:
Bibliographic Details
Published in:Journal of physical chemistry. C 2018-01, Vol.122 (1), p.349-358
Main Authors: Qian, Jiajia, Shen, Chao, Yan, Jing, Xi, Fengna, Dong, Xiaoping, Liu, Jiyang
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Graphene quantum dots (GQDs) as new 0-dimensional (0D) materials have exhibited promising applications in numerous fields, and these enormous potentials are largely dependent on their electronic properties. Herein we tailored the semiconductive behavior of GQDs and transformed the n-type hydrothermally synthesized GQDs to p-type via the modification of PO groups with an electron-withdrawing ability. The obtained highly dispersed and stable P-doped GQDs (P-GQDs) had uniform size and thickness, high crystallinity, and wide visible-light absorption region. The subsequent assembly with the n-type graphitic carbon nitride (CN) formed a stable metal-free photocatalyst because of the π–π interaction between conjugated GQDs sheets and CN layers and the possible hydrogen bonds as well. Due to the formation of p–n junction on the P-GQDs/CN interface, the photogenerated charges were efficiently separated which resulted in an enhanced photocatalytic performance. This strategy illuminates the GQDs applications by controlling the electronic structure of GQDs based on the detailed application, not only for photocatalysis but also for many other fields such as solar cells, catalysis, electrocatalysis, and so on.
ISSN:1932-7447
1932-7455
DOI:10.1021/acs.jpcc.7b08702