12 research outputs found
PS-micelles altered the Φ<sub>s</sub> distribution histogram.
<p>Figures A and B show the AFM and KPFM images, respectively, of a PC12 cell treated with PS-micelles. C. The Φ<sub>s</sub> from B was binned with 40 steps and the histogram was fitted with a two-peak Gaussian model (red line). The two Gaussian distributions were plotted in green and blue. D. Averaged skewness in PC12 cells without treatment (control) or treated with PC- and PS-micelles (PC & PS, respectively). Data are expressed as mean ± SEM, and N = 11 for each group. * indicates <i>p</i><0.05 (by Student's <i>t</i>-test) compared with the control group.</p
Various Φ<sub>s</sub> distribution histograms of PC12 cell plasma membrane.
<p>A fixed PC12 cell was air-dried and then a 66 µm<sup>2</sup> region of the plasma membrane was scanned at a resolution of 256128 pixels. Figures A and B show the simultaneously recorded AFM and KPFM images, respectively. C. The Φ<sub>s</sub> from B was binned with 40 steps and the histogram was fitted with a two-peak Gaussian model (red line). The two Gaussian peaks were plotted in green and blue. D–E. Two other representative cells having Φ<sub>s</sub> distribution histograms with differing skewness values.</p
An Ultrasensitive Nanowire-Transistor Biosensor for Detecting Dopamine Release from Living PC12 Cells under Hypoxic Stimulation
Dopamine (DA) is
an important neurotransmitter that is involved
in neuronal signal transduction and several critical illnesses. However,
the concentration of DA is extremely low in patients and is difficult
to detect using existing electrochemical biosensors with detection
limits typically around nanomolar levels (∼10<sup>–9</sup> M). Here, we developed a nanoelectronic device as a biosensor for
ultrasensitive and selective DA detection by modifying DNA-aptamers
on a multiple-parallel-connected (MPC) silicon nanowire field-effect
transistor (referred to as MPC aptamer/SiNW-FET). Compared with conventional
electrochemical methods, the MPC aptamer/SiNW-FET has been demonstrated
to improve the limit of DA detection to <10<sup>–11</sup> M and to possess a detection specificity that is able to distinguish
DA from other chemical analogues, such as ascorbic acid, catechol,
phenethylamine, tyrosine, epinephrine, and norepinephrine. This MPC
aptamer/SiNW-FET was also applied to monitor DA release under hypoxic
stimulation from living PC12 cells. The real-time recording of the
exocytotic DA induced by hypoxia reveals that the increase in intracellular
Ca<sup>2+</sup> that is required to trigger DA secretion is dominated
by an extracellular Ca<sup>2+</sup> influx, rather than the release
of intracellular Ca<sup>2+</sup> stores
One-Step Synthesis of Antioxidative Graphene-Wrapped Copper Nanoparticles on Flexible Substrates for Electronic and Electrocatalytic Applications
In
this study, we report a novel, one-step synthesis method to fabricate
multilayer graphene (MLG)-wrapped copper nanoparticles (CuNPs) directly
on various substrates (e.g., polyimide film (PI), carbon cloth (CC),
or Si wafer (Si)). The electrical resistivities of the pristine MLG-CuNPs/PI
and MLG-CuNPs/Si were measured 1.7 × 10<sup>–6</sup> and
1.4 × 10<sup>–6</sup> Ω·m, respectively, of
which both values are ∼100-fold lower than earlier reports.
The MLG shell could remarkably prevent the Cu nanocore from serious
damages after MLG-CuNPs being exposed to various harsh conditions.
Both MLG-CuNPs/PI and MLG-CuNPs/Si retained almost their conductivities
after ambient annealing at 150 °C. Furthermore, the flexible
MLG-CuNPs/PI exhibits excellent mechanical durability after 1000 bending
cycles. We also demonstrate that the MLG-CuNPs/PI can be used as promising
source-drain electrodes in fabricating flexible graphene-based field-effect
transistor (G-FET) devices. Finally, the MLG-CuNPs/CC was shown to
possess high performance and durability toward hydrogen evolution
reaction (HER)
Growth of Large-Area Graphene Single Crystals in Confined Reaction Space with Diffusion-Driven Chemical Vapor Deposition
To synthesize large-area graphene
single crystals, we specifically
designed a low-pressure chemical vapor deposition (LPCVD) reactor
with confined reaction space (L 22 mm × W 13 mm × H 50 μm).
Within the confined reaction space, a uniform distribution of reactant
concentrations, reduced substrate roughness, and the shift of growth
kinetics toward a diffusion-limited regime can be achieved, favoring
the preparation of large-area, high-quality graphene single crystals.
The gas flow field and mass transport pattern of reactants in the
LPCVD system simulated with a finite element method support the advantages
of using this confined reaction room for graphene growth. Using this
space-confined reactor together with the optimized synthesis parameters,
we obtained monolayer, highly uniform, and defect-free graphene single
crystals of up to ∼0.8 mm in diameter with the field-effect
mobility of μ<sub>EF</sub> ∼ 4800 cm<sup>2</sup> V<sup>–1</sup> s<sup>–1</sup> at room temperature. In addition,
structural design of the confined reaction space by adjusting the
reactor’s dimensions is of facile controllability and scalability,
which demonstrates the superiority and preference of this method for
industrial applications
Three-Dimensional Heterostructures of MoS<sub>2</sub> Nanosheets on Conducting MoO<sub>2</sub> as an Efficient Electrocatalyst To Enhance Hydrogen Evolution Reaction
Molybdenum
disulfide (MoS<sub>2</sub>) is a promising catalyst
for hydrogen evolution reaction (HER) because of its unique nature
to supply active sites in the reaction. However, the low density of
active sites and their poor electrical conductivity have limited the
performance of MoS<sub>2</sub> in HER. In this work, we synthesized
MoS<sub>2</sub> nanosheets on three-dimensional (3D) conductive MoO<sub>2</sub> via a two-step chemical vapor deposition (CVD) reaction.
The 3D MoO<sub>2</sub> structure can create structural disorders in
MoS<sub>2</sub> nanosheets (referred to as 3D MoS<sub>2</sub>/MoO<sub>2</sub>), which are responsible for providing the superior HER activity
by exposing tremendous active sites of terminal disulfur of S<sub>2</sub><sup>–2</sup> (in MoS<sub>2</sub>) as well as the backbone conductive oxide layer (of MoO<sub>2</sub>) to facilitate an interfacial charge transport for the proton
reduction. In addition, the MoS<sub>2</sub> nanosheets could protect
the inner MoO<sub>2</sub> core from the acidic electrolyte in the
HER. The high activity of the as-synthesized 3D MoS<sub>2</sub>/MoO<sub>2</sub> hybrid material in HER is attributed to the small onset overpotential
of 142 mV, a largest cathodic current density of 85 mA cm<sup>–2</sup>, a low Tafel slope of 35.6 mV dec<sup>–1</sup>, and robust
electrochemical durability
Tuning Rashba Spin–Orbit Coupling in Gated Multilayer InSe
Manipulating
the electron spin with the aid of spin–orbit
coupling (SOC) is an indispensable element of spintronics. Electrostatically
gating a material with strong SOC results in an effective magnetic
field which can in turn be used to govern the electron spin. In this
work, we report the existence and electrostatic tunability of Rashba
SOC in multilayer InSe. We observed a gate-voltage-tuned crossover
from weak localization (WL) to weak antilocalization (WAL) effect
in quantum transport studies of InSe, which suggests an increasing
SOC strength. Quantitative analyses of magneto-transport studies and
energy band diagram calculations provide strong evidence for the predominance
of Rashba SOC in electrostatically gated InSe. Furthermore, we attribute
the tendency of the SOC strength to saturate at high gate voltages
to the increased electronic density of states-induced saturation of
the electric field experienced by the electrons in the InSe layer.
This explanation of nonlinear gate voltage control of Rashba SOC can
be generalized to other electrostatically gated semiconductor nanomaterials
in which a similar tendency of spin–orbit length saturation
was observed (e.g., nanowire field effect transistors), and is thus
of broad implications in spintronics. Identifying and controlling
the Rashba SOC in InSe may serve pivotally in devising III–VI
semiconductor-based spintronic devices in the future
Intrinsic Electron Mobility Exceeding 10<sup>3</sup> cm<sup>2</sup>/(V s) in Multilayer InSe FETs
Graphene-like two-dimensional (2D)
materials not only are interesting for their exotic electronic structure
and fundamental electronic transport or optical properties but also
hold promises for device miniaturization down to atomic thickness.
As one material belonging to this category, InSe, a III–VI
semiconductor, not only is a promising candidate for optoelectronic
devices but also has potential for ultrathin field effect transistor
(FET) with high mobility transport. In this work, various substrates
such as PMMA, bare silicon oxide, passivated silicon oxide, and silicon
nitride were used to fabricate multilayer InSe FET devices. Through
back gating and Hall measurement in four-probe configuration, the
device’s field effect mobility and intrinsic Hall mobility
were extracted at various temperatures to study the material’s
intrinsic transport behavior and the effect of dielectric substrate.
The sample’s field effect and Hall mobilities over the range
of 20–300 K fall in the range of 0.1–2.0 × 10<sup>3</sup> cm<sup>2</sup>/(V s), which are comparable or better than
the state of the art FETs made of widely studied 2D transition metal
dichalcogenides
Improving Nanowire Sensing Capability by Electrical Field Alignment of Surface Probing Molecules
We
argue that the structure ordering of self-assembled probing molecular
monolayers is essential for the reliability and sensitivity of nanowire-based
field-effect sensors because it can promote the efficiency for molecular
interactions as well as strengthen the molecular dipole field experienced
by the nanowires. In the case of monolayers, we showed that structure
ordering could be improved by means of electrical field alignment.
This technique was then employed to align multilayer complexes for
nanowire sensing applications. The sensitivity we achieved for detection
of hybridization between 15-base single-strand DNA molecules is 0.1
fM and for alcohol sensors is 0.5 ppm. The reliability was confirmed
by repeated tests on chips that contain multiple nanowire sensors
High Performance and Bendable Few-Layered InSe Photodetectors with Broad Spectral Response
Two-dimensional crystals with a wealth
of exotic dimensional-dependent
properties are promising candidates for next-generation ultrathin
and flexible optoelectronic devices. For the first time, we demonstrate
that few-layered InSe photodetectors, fabricated on both a rigid SiO<sub>2</sub>/Si substrate and a flexible polyethylene terephthalate (PET)
film, are capable of conducting broadband photodetection from the
visible to near-infrared region (450–785 nm) with high photoresponsivities
of up to 12.3 AW<sup>–1</sup> at 450 nm (on SiO<sub>2</sub>/Si) and 3.9 AW<sup>–1</sup> at 633 nm (on PET). These photoresponsivities
are superior to those of other recently reported two-dimensional (2D)
crystal-based (graphene, MoS<sub>2</sub>, GaS, and GaSe) photodetectors.
The InSe devices fabricated on rigid SiO<sub>2</sub>/Si substrates
possess a response time of ∼50 ms and exhibit long-term stability
in photoswitching. These InSe devices can also operate on a flexible
substrate with or without bending and reveal comparable performance
to those devices on SiO<sub>2</sub>/Si. With these excellent optoelectronic
merits, we envision that the nanoscale InSe layers will not only find
applications in flexible optoelectronics but also act as an active
component to configure versatile 2D heterostructure devices