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NanoMat 2018

Nano Research & Applications

ISSN: 2471-9838

Page 45

April 26-27, 2018

Rome, Italy

17

th

Edition of International Conference on

Emerging Trends in

Materials Science and

Nanotechnology

O

ne of the emerging applications exploring the potentialities

of fluorescent nanomaterials is related to light emitting

technologies. In particular for the realization of practical

light- emitting diodes and large-area displays, semiconductor

nanomaterials may overcome many issues of such challenging

technologies. A critical aspect of semiconductor nanoscaled

materials is related to the large Coulomb interaction between

electrons and holes, and their strong spatial confinement, with

respect to their bulk analogues. When the size is reduced to levels

smaller than the exciton Bohr radius, size-dependent absorption

and emission properties develop. Upon formation of excitons

within quantumdots (QDs) through optical or electrical processes,

Coulomb interactions play a key role in subsequently determining

their radiative and nonradiative decay rates, fluorescence

quantum yields, multi-exciton generation and its decay.

Appropriate engineering of QDs, through the colloidal synthesis

of core/shell heterostructures, has emerged as the most facile

manner to gain control of these Coulomb processes. The strong

electronic coupling between the core and shell in core/shell QDs,

ensures that the electronic structure, composition and thickness

of the shell must be considered in parallel with the properties

of the core in order to predictably manipulate the electron and

hole probability densities to obtain the desired optoelectronic

characteristics. This spatial control of carriers affects the direct

Coulomb interaction between electrons and holes, but also

influences the rate and carrier selectivity of trapping at surface

and, possibly interfaces defects. The latter is highly dependent

on the core/shell structure, for which lattice mismatch between

materials must be carefully managed to avoid defect formation

stemming from excessive interfacial stress. The above structural

and electronic factors define the dynamics of single and multi

excitons in QDs, which directly influences aspects such as

recombination lifetimes, luminescence efficiency and optical

gain properties. Considering the importance of each of these

properties for light emitting applications, in this presentation

we compare different approaches for the enhancement of light

emission quality in terms of high fluorescence efficiency, high

color quality, enhanced photostability under prolonged irradiation

and easy implementation of solution processablemethodologies.

All these excellent features make the use of QDs materials a

promising way for the realization of optically and electrically

pumped light emitting devices.

Recent Publications

1. Minotto A, Todescato F, Fortunati I, Signorini R,

Jasieniak J J and Bozio R (2014) Role of Core-Shell

Interfaces on Exciton Recombination in CdSe-CdxZn1-

xS Quantum Dots. The Journal of Physical Chemistry

C 118(41):24117-24126.

2. Fede C, Fortunati I,Weber W, Rossetto N, Bertasi F,

Petrelli L, Guidolin D, Signorini R, De Caro R, Albertin G

and Ferrante C (2015) Evaluation of gold nanoparticles

toxicity towards human endothelial cells under static

and flow conditions. Microvascular Research 97:147-155.

3. Vittadello L, Zaltron A, Argiolas N, Bazzan M, Rossetto

N and Signorini R (2016) Photorefractive direct

laser writing. Journal of Physics D: Applied Physics

49:125103-125111.

Semiconductor quantum dots for light emitting applications

Raffaella Signorini

1

, Francesco Todescato

1

, Ilaria Fortunati

1

, Alessandro Minot-

to

1

, Jacek J Jasieniak

2

and

Renato Bozio

1

1

INSTM - University of Padova, Italy

2

Monash University, Australia

Raffaella Signorini et al., Nano Res Appl, Volume:4

DOI: 10.21767/2471-9838-C1-008

Figure 1:

Cross-‐sectional core-‐shell structure depiction and

a schematic representation of the electronic (hole) density

distribution of CdSe-‐CdS, CdSe-‐Cd0.5Zn0.5S and CdSe-‐

CdS-‐ Cd0.5Zn0.5S-‐ZnS QDs.