Issue 40, 2016

Molecular origin of photoluminescence of carbon dots: aggregation-induced orange-red emission

Abstract

The molecular origin of the photoluminescence of carbon dots (CDs) is not known. This restricts the design of CDs with desired optical properties. We have synthesized CDs starting from carbohydrates by employing a simple synthesis method. We were able to demonstrate that the CDs are composed of aggregated hydroxymethylfurfural (HMF) derivatives. The optical properties of these CDs are quite unique. These CDs exhibit an excitation-independent PL emission maximum in the orange-red region (λmaxem ∼ 590 nm). These CDs also exhibit excitation as well as monitoring wavelength-independent single exponential PL decay. These observations indicate that only one type of chromophore (HMF derivative) is present within the CDs. Several HMF derivatives are aggregated within the CDs; therefore, the aggregated structure cause a large Stokes shift (∼150 nm). By several control experiments, we showed that the same aggregated chromophore unit (HMF derivative), and not the individual fluorophores, is the fluorescing unit. The emission maximum and the single exponential PL lifetime are independent of the polarity of the medium. The existence of a low-lying trap state could be reduced quite significantly. A model has been proposed to explain the interesting steady state and dynamical photoluminescence behaviour of the CDs. As the molecular origin of their photoluminescence is known, CDs with desired optical properties can be designed.

Graphical abstract: Molecular origin of photoluminescence of carbon dots: aggregation-induced orange-red emission

Supplementary files

Article information

Article type
Paper
Submitted
01 Aug. 2016
Accepted
16 Sept. 2016
First published
16 Sept. 2016
This article is Open Access
Creative Commons BY-NC license

Phys. Chem. Chem. Phys., 2016,18, 28274-28280

Molecular origin of photoluminescence of carbon dots: aggregation-induced orange-red emission

V. Gude, A. Das, T. Chatterjee and P. K. Mandal, Phys. Chem. Chem. Phys., 2016, 18, 28274 DOI: 10.1039/C6CP05321A

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