5 research outputs found
Ultrafast Control of Phase and Polarization of Light Expedited by Hot-Electron Transfer
All-optical
modulation is an entangled part of ultrafast nonlinear
optics with promising impacts on tunable optical devices in the future.
Current advancements in all-optical control predominantly offer modulation
by means of altering light intensity, while the ultrafast manipulation
of other attributes of light have yet to be further explored. Here,
we demonstrate the active modulation of the phase, polarization, and
amplitude of light through the nonlinear modification of the optical
response of a plasmonic crystal that supports subradiant, high Q,
and polarization-selective resonance modes. The designed mode is exclusively
accessible via TM-polarized light, which enables significant phase
modulation and polarization conversion within the visible spectrum.
To tailor the device performance in the time domain, we exploit the
ultrafast transport dynamics of hot electrons at the interface of
plasmonic metals and charge acceptor materials to facilitate an ultrafast
switching speed. In addition, the operating wavelength of the proposed
device can be tuned through the control of the in-plane momentum of
light. Our work reveals the viability of dynamic phase and polarization
control in plasmonic systems for all-optical switching and data processing
Resonant Light-Induced Heating in Hybrid Cavity-Coupled 2D Transition-Metal Dichalcogenides
Hybrid structures based on integration
of two-dimensional (2D)
transition-metal dichalcogenides (TMDCs) with optical resonators have
recently earned significant attention. The enhanced interaction of
light with 2D materials in such hybrid structures can enable devices
such as efficient light-emitting diodes and lasers. However, one of
the factors affecting the performance of such devices is the effect
of the optically induced heat on the optoelectronic properties of
the 2D materials. In this study, we systematically investigate principal
roots of heat generation in hybrid cavity-coupled few-atomic-layer-thick
2D TMDC films under optical pumping. The optical resonator exploited
here is a Fabry–Perot (FP) resonator, which can enhance the
light–MoS<sub>2</sub> interaction by a significant factor of
60 at its resonance wavelength. We have combined an accurate theoretical
modeling with experimental Raman spectroscopy to determine the roots
of heat generation in MoS<sub>2</sub> films integrated with FP resonators.
Our investigations reveal that the strong modulation of light absorption
in the MoS<sub>2</sub> film, induced by excitation of an FP cavity
at its resonant frequency, plays the primary role in excess heat generation
in 2D materials. Furthermore, through varying the cavity length, we
show that on-resonance and off-resonance excitation of the cavity
results in completely different temperature profiles in the cavity-coupled
MoS<sub>2</sub> films. Also, by changing the resonance medium of the
FP cavity (SiO<sub>2</sub> and air), we take into account the role
of the heat sinking effect of the substrate in heat generation in
MoS<sub>2</sub> films. In this study, the temperature-dependent red-shift
of the Raman spectra is employed to monitor the local temperature
of the MoS<sub>2</sub> films. Our results show the importance of the
heating effect in such hybrid structures and represent a step forward
for the design of practical hybrid optical devices based on layered
semiconducting 2D materials
Cell-Imprinted Substrates Act as an Artificial Niche for Skin Regeneration
Bioinspired materials
can mimic the stem cell environment and modulate
stem cell differentiation and proliferation. In this study, biomimetic
micro/nanoenvironments were fabricated by cell-imprinted substrates
based on mature human keratinocyte morphological templates. The data
obtained from atomic force microscopy and field emission scanning electron microscopy revealed that the keratinocyte-cell-imprinted poly(dimethylsiloxane) casting procedure could imitate the surface morphology of the plasma membrane, ranging from the nanoscale to the macroscale, which may provide the required topographical cell fingerprints to induce differentiation. Gene expression levels of the genes analyzed (involucrin, collagen type I, and keratin 10) together with protein expression data showed that human adipose-derived stem cells (ADSCs) seeded on these cell-imprinted substrates were driven to adopt the specific shape and characteristics of keratinocytes. The observed morphology of the ADSCs grown on the keratinocyte casts was noticeably different from that of stem cells cultivated on the stem-cell-imprinted substrates. Since the shape and geometry of the nucleus could potentially alter the gene expression, we used molecular dynamics to probe the effect of the confining geometry on the chain arrangement of simulated chromatin fibers in the nuclei. The results obtained suggested that induction of mature cell shapes onto stem cells can influence nucleus deformation of the stem cells followed by regulation of target genes. This might pave the way for a reliable, efficient, and cheap approach of controlling stem cell differentiation toward skin cells for wound healing applications
Cell-Imprinted Substrates Act as an Artificial Niche for Skin Regeneration
Bioinspired materials
can mimic the stem cell environment and modulate
stem cell differentiation and proliferation. In this study, biomimetic
micro/nanoenvironments were fabricated by cell-imprinted substrates
based on mature human keratinocyte morphological templates. The data
obtained from atomic force microscopy and field emission scanning electron microscopy revealed that the keratinocyte-cell-imprinted poly(dimethylsiloxane) casting procedure could imitate the surface morphology of the plasma membrane, ranging from the nanoscale to the macroscale, which may provide the required topographical cell fingerprints to induce differentiation. Gene expression levels of the genes analyzed (involucrin, collagen type I, and keratin 10) together with protein expression data showed that human adipose-derived stem cells (ADSCs) seeded on these cell-imprinted substrates were driven to adopt the specific shape and characteristics of keratinocytes. The observed morphology of the ADSCs grown on the keratinocyte casts was noticeably different from that of stem cells cultivated on the stem-cell-imprinted substrates. Since the shape and geometry of the nucleus could potentially alter the gene expression, we used molecular dynamics to probe the effect of the confining geometry on the chain arrangement of simulated chromatin fibers in the nuclei. The results obtained suggested that induction of mature cell shapes onto stem cells can influence nucleus deformation of the stem cells followed by regulation of target genes. This might pave the way for a reliable, efficient, and cheap approach of controlling stem cell differentiation toward skin cells for wound healing applications
Cell-Imprinted Substrates Act as an Artificial Niche for Skin Regeneration
Bioinspired materials
can mimic the stem cell environment and modulate
stem cell differentiation and proliferation. In this study, biomimetic
micro/nanoenvironments were fabricated by cell-imprinted substrates
based on mature human keratinocyte morphological templates. The data
obtained from atomic force microscopy and field emission scanning electron microscopy revealed that the keratinocyte-cell-imprinted poly(dimethylsiloxane) casting procedure could imitate the surface morphology of the plasma membrane, ranging from the nanoscale to the macroscale, which may provide the required topographical cell fingerprints to induce differentiation. Gene expression levels of the genes analyzed (involucrin, collagen type I, and keratin 10) together with protein expression data showed that human adipose-derived stem cells (ADSCs) seeded on these cell-imprinted substrates were driven to adopt the specific shape and characteristics of keratinocytes. The observed morphology of the ADSCs grown on the keratinocyte casts was noticeably different from that of stem cells cultivated on the stem-cell-imprinted substrates. Since the shape and geometry of the nucleus could potentially alter the gene expression, we used molecular dynamics to probe the effect of the confining geometry on the chain arrangement of simulated chromatin fibers in the nuclei. The results obtained suggested that induction of mature cell shapes onto stem cells can influence nucleus deformation of the stem cells followed by regulation of target genes. This might pave the way for a reliable, efficient, and cheap approach of controlling stem cell differentiation toward skin cells for wound healing applications