Scinovex
reviewTop 1% cited

Graphene quantum dots: emergent nanolights for bioimaging, sensors, catalysis and photovoltaic devices

Chemical Communications · 2012 · Vol. 48(31) · pp. 3686–3686
Jianhua ShenYihua ZhuXiaoling YangChunzhong Li

Abstract

Similar to the popular older cousins, luminescent carbon dots (C-dots), graphene quantum dots or graphene quantum discs (GQDs) have generated enormous excitement because of their superiority in chemical inertness, biocompatibility and low toxicity. Besides, GQDs, consisting of a single atomic layer of nano-sized graphite, have the excellent performances of graphene, such as high surface area, large diameter and better surface grafting using π-π conjugation and surface groups. Because of the structure of graphene, GQDs have some other special physical properties. Therefore, studies on GQDs in aspects of chemistry, physical, materials, biology and interdisciplinary science have been in full flow in the past decade. In this Feature Article, recent developments in preparation of GQDs are discussed, focusing on the main two approaches (top-down and bottom-down). Emphasis is given to their future and potential development in bioimaging, electrochemical biosensors and catalysis, and specifically in photovoltaic devices that can solve increasingly serious energy problems.

Carbon and Quantum Dots ApplicationsGraphene and Nanomaterials ApplicationsNanocluster Synthesis and ApplicationsGrapheneQuantum dotNanotechnologyMaterials sciencePhotovoltaic systemBiosensorGraphene quantum dotGraphiteBiocompatibility

MeSH terms

CatalysisDiagnostic ImagingGraphiteHumansBiosensing TechniquesQuantum DotsPhotochemical Processes

Funding

  • National Natural Science Foundation of China
  • Fundamental Research Funds for the Central Universities
  • Program for Changjiang Scholars and Innovative Research Team in University
Citations
2,030
FWCI
71.21
field-weighted impact
References
114
Percentile
100%
vs. same field & year
Citations per year
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.