Here we designed and synthesized CdSe/CdSe 1−x Te x core/crown nanoplatelets (NPLs) with controlled crown compositions by using the core-seeded-growth approach. We confirmed the uniform growth of the crown regions with well-defined shape and compositions by employing transmission electron microscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. By precisely tuning the composition of the CdSe 1−x Te x crown region from pure CdTe (x = 1.00) to almost pure CdSe doped with several Te atoms (x = 0.02), we achieved tunable excitonic properties without changing the thickness of the NPLs and demonstrated the evolution of type-II electronic structure. Upon increasing the Te concentration in the crown region, we obtained continuously tunable photoluminescence peaks within the range of ∼570 nm (for CdSe 1−x Te x crown with x = 0.02) and ∼660 nm (for CdSe 1−x Te x crown with x = 1.00). Furthermore, with the formation of the CdSe 1−x Te x crown region, we observed substantially improved photoluminescence quantum yields (up to ∼95%) owing to the suppression of nonradiative hole trap sites. Also, we found significantly increased fluorescence lifetimes from ∼49 up to ∼326 ns with increasing Te content in the crown, suggesting the transition from quasi-type-II to type-II electronic structure. With their tunable excitonic properties, this novel material presented here will find ubiquitous use in various efficient light-emitting and-harvesting applications.
Here, we designed
and synthesized alloyed heterostructures of CdSe
x
S1–x
nanoplatelets
(NPLs) using CdS coating in the lateral and vertical directions for
the achievement of highly tunable optical gain performance. By using
homogeneously alloyed CdSe
x
S1–x
core NPLs as a seed, we prepared CdSe
x
S1–x
/CdS core/crown
NPLs, where CdS crown region is extended only in the lateral direction.
With the sidewall passivation around inner CdSe
x
S1–x
cores, we achieved
enhanced photoluminescence quantum yield (PL-QY) (reaching 60%), together
with increased absorption cross-section and improved stability without
changing the emission spectrum of CdSe
x
S1–x
alloyed core NPLs. In addition,
we further extended the spectral tunability of these solution-processed
NPLs with the synthesis of CdSe
x
S1–x
/CdS core/shell NPLs. Depending
on the sulfur composition of the CdSe
x
S1–x
core and thickness of the
CdS shell, CdSe
x
S1–x
/CdS core/shell NPLs possessed highly tunable emission
characteristics within the spectral range of 560–650 nm. Finally,
we studied the optical gain performances of different heterostructures
of CdSe
x
S1–x
alloyed NPLs offering great advantages, including reduced
reabsorption and spectrally tunable optical gain range. Despite their
decreased PL-QY and reduced absorption cross-section upon increasing
the sulfur composition, CdSe
x
S1–x
based NPLs exhibit highly tunable amplified spontaneous
emission performance together with low gain thresholds down to ∼53
μJ/cm2.
Membrane antigens are phenotypic signatures of cells used for distinguishing various subpopulations and therefore, are of great interest for diagnosis diseases and monitoring of patient in hematology and oncology. Existing...
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