4 research outputs found
Flexible, Transparent, and Noncytotoxic Graphene Electric Field Stimulator for Effective Cerebral Blood Volume Enhancement
Enhancing cerebral blood volume (CBV) of a targeted area without causing side effects is a primary strategy for treating cerebral hypoperfusion. Here, we report a new nonpharmaceutical and nonvascular surgical method to increase CBV. A flexible, transparent, and skin-like biocompatible graphene electrical field stimulator was placed directly onto the cortical brain, and a noncontact electric field was applied at a specific local blood vessel. Effective CBV increases in the blood vessels of mouse brains were directly observed from <i>in vivo</i> optical recordings of intrinsic signal imaging. The CBV was significantly increased in arteries of the stimulated area, but neither tissue damage nor unnecessary neuronal activation was observed. No transient hypoxia was observed. This technique provides a new method to treat cerebral blood circulation deficiencies at local vessels and can be applied to brain regeneration and rehabilitation
Mixed Copper States in Anodized Cu Electrocatalyst for Stable and Selective Ethylene Production from CO<sub>2</sub> Reduction
Oxygen–Cu
(O–Cu) combination catalysts have recently
achieved highly improved selectivity for ethylene production from
the electrochemical CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR). In this study, we developed anodized copper (AN-Cu) CuÂ(OH)<sub>2</sub> catalysts by a simple electrochemical synthesis method and
achieved ∼40% Faradaic efficiency for ethylene production,
and high stability over 40 h. Notably, the initial reduction conditions
applied to AN-Cu were critical to achieving selective and stable ethylene
production activity from the CO<sub>2</sub>RR, as the initial reduction
condition affects the structures and chemical states, crucial for
highly selective and stable ethylene production over methane. A highly
negative reduction potential produced a catalyst maintaining long-term
stability for the selective production of ethylene over methane, and
a small amount of CuÂ(OH)<sub>2</sub> was still observed on the catalyst
surface. Meanwhile, when a mild reduction condition was applied to
the AN-Cu, the CuÂ(OH)<sub>2</sub> crystal structure and mixed states
disappeared on the catalyst, becoming more favorable to methane production
after few hours. These results show the selectivity of ethylene to
methane in O–Cu combination catalysts is influenced by the
electrochemical reduction environment related to the mixed valences.
This will provide new strategies to improve durability of O–Cu
combination catalysts for C–C coupling products from electrochemical
CO<sub>2</sub> conversion
Modulating Electronic Properties of Monolayer MoS<sub>2</sub> <i>via</i> Electron-Withdrawing Functional Groups of Graphene Oxide
Modulation of the
carrier concentration and electronic type of
monolayer (1L) MoS<sub>2</sub> is highly important for applications
in logic circuits, solar cells, and light-emitting diodes. Here, we
demonstrate the tuning of the electronic properties of large-area
1L-MoS<sub>2</sub> using graphene oxide (GO). GO sheets are well-known
as hole injection layers since they contain electron-withdrawing groups
such as carboxyl, hydroxyl, and epoxy. The optical and electronic
properties of GO-treated 1L-MoS<sub>2</sub> are dramatically changed.
The photoluminescence intensity of GO-treated 1L-MoS<sub>2</sub> is
increases by more than 470% compared to the pristine sample because
of the increase in neutral exciton contribution. In addition, the
A<sub>1g</sub> peak in Raman spectra shifts considerably, revealing
that GO treatment led to the formation of p-type doped 1L-MoS<sub>2</sub>. Moreover, the current <i>vs</i> voltage (<i>I–V</i>) curves of GO-coated 1L-MoS<sub>2</sub> field
effect transistors show that the electron concentration of 1L-MoS<sub>2</sub> is significantly lower in comparison with pristine 1L-MoS<sub>2</sub>. Current rectification is also observed from the <i>I–V</i> curve of the lateral diode structure with 1L-MoS<sub>2</sub> and 1L-MoS<sub>2</sub>/GO, indicating that the electronic
structure of MoS<sub>2</sub> is significantly modulated by the electron-withdrawing
functional group of GO
Large Work Function Modulation of Monolayer MoS<sub>2</sub> by Ambient Gases
Although
two-dimensional monolayer transition-metal dichalcogenides
reveal numerous unique features that are inaccessible in bulk materials,
their intrinsic properties are often obscured by environmental effects.
Among them, work function, which is the energy required to extract
an electron from a material to vacuum, is one critical parameter in
electronic/optoelectronic devices. Here, we report a large work function
modulation in MoS<sub>2</sub> via ambient gases. The work function
was measured by an <i>in situ</i> Kelvin probe technique
and further confirmed by ultraviolet photoemission spectroscopy and
theoretical calculations. A measured work function of 4.04 eV in vacuum
was converted to 4.47 eV with O<sub>2</sub> exposure, which is comparable
with a large variation in graphene. The homojunction diode by partially
passivating a transistor reveals an ideal junction with an ideality
factor of almost one and perfect electrical reversibility. The estimated
depletion width obtained from photocurrent mapping was ∼200
nm, which is much narrower than bulk semiconductors