4 research outputs found
From Large-Scale Synthesis to Lighting Device Applications of Ternary I–III–VI Semiconductor Nanocrystals: Inspiring Greener Material Emitters
Quantum dots with
fabulous size-dependent and color-tunable emissions
remained as one of the most exciting inventories in nanomaterials
for the last 3 decades. Even though a large number of such dot nanocrystals
were developed, CdSe still remained as unbeatable and highly trusted
lighting nanocrystals. Beyond these, the ternary I–III–VI
family of nanocrystals emerged as the most widely accepted greener
materials with efficient emissions tunable in visible as well as NIR
spectral windows. These bring the high possibility of their implementation
as lighting materials acceptable to the community and also to the
environment. Keeping these in mind, in this Perspective, the latest
developments of ternary I–III–VI nanocrystals from their
large-scale synthesis to device applications are presented. Incorporating
ZnS, tuning the composition, mixing with other nanocrystals, and doping
with Mn ions, light-emitting devices of single color as well as for
generating white light emissions are also discussed. In addition,
the future prospects of these materials in lighting applications are
also proposed
Hydroxyl-Terminated CuInS<sub>2</sub> Based Quantum Dots: Toward Efficient and Bright Light Emitting Diodes
CuInS<sub>2</sub> based quantum dots
are emerging as low toxic
materials for new generation white lighting technology due to their
broad and color-tunable emissions as well as large Stokes shifts.
Here, we developed a simple and <i>in situ</i> ligand exchange
strategy for the fabrication of hydroxyl-terminated CuInS<sub>2</sub> based quantum dots capped with 6-mercaptohexanol. During the ligand
exchange, long-chain methyl-terminated oleylamine on the quantum dots’
surface can be effectively and efficiently replaced by the short-chain
hydroxyl-terminated 6-mercaptohexanol, enabling their solubility in
polar organic solvents such as methanol, ethanol, and dimethylformamide.
Moreover, the resulting hydroxyl-terminated quantum dots exhibit well-preserved
photoluminescence properties with quantum yields of ∼70%. Using
these hydroxyl-terminated CuInS<sub>2</sub> based quantum dots as
an emitting layer, we fabricated efficient and bright light emitting
diodes by adopting an inverted device structure. The optimized devices
show a maximum luminance of 8,735 cd/m<sup>2</sup> and an external
quantum efficiency of 3.22%. Furthermore, the performance enhancement
can be explained by considering the decreased energy barriers between
the electron transport layer and the emitting layer. The combination
of high efficiency and enhanced brightness as well as the potential
all-solution processability using green solvents makes hydroxyl-terminated
quantum dots capped with 6-mercaptohexanol a new generation of materials
for light emitting applications
Template Synthesis of CuInS<sub>2</sub> Nanocrystals from In<sub>2</sub>S<sub>3</sub> Nanoplates and Their Application as Counter Electrodes in Dye-Sensitized Solar Cells
We
report the room temperature template synthesis of CuInS<sub>2</sub> nanocrystals through incorporation of Cu<sup>+</sup> cations
into In<sub>2</sub>S<sub>3</sub> nanoplates whose chemical composition
has been controlled by varying the amount of copper ions in the reaction
mixture. As a result, bandgaps of the resultant CuInS<sub>2</sub> nanoplates
can be tuned from 1.45 to 1.19 eV with [Cu]/[In] molar ratios increasing
from 0.7 to 2.9, which was demonstrated by the cyclic voltammetry.
We explored the use of CuInS<sub>2</sub> nanocrystals as potential
counter electrodes in dye-sensitized solar cells, and a power conversion
efficiency of 6.83% was achieved without selenization and ligand exchange.
The value is comparable with the performance of a control device using
Pt as a counter electrode (power conversion efficiency: 7.08%) under
the same device architecture