7 research outputs found
Superconductivity in Potassium-Doped Few-Layer Graphene
Here we report the successful synthesis of superconducting
potassium-doped
few-layer graphene (K-doped FLG) with a transition temperature of
4.5 K, which is 1 order of magnitude higher than that observed in
the bulk potassium graphite intercalation compound (GIC) KC<sub>8</sub> (<i>T</i><sub>c</sub> = 0.39 K). The realization of superconductivity
in K-doped FLG shows the potential for the development of new superconducting
electronic devices using two-dimensional (2D) graphene as a basis
material
Mutual Independence Ensured Long-Term Cycling Stability: Template-Free Electrodeposited Sn<sub>4</sub>Ni<sub>3</sub> Nanoparticles as Anode Material for Lithium-Ion Batteries
The key challenge
in utilizing tin-based intermetallic compounds for lithium-ion batteries
(LIBs) is the poor cycling stability which is caused by the huge volume
change during the alloying/de-alloying processes. In this work, concerning
this issue, a novel template-free electrodeposition procedure to prepare
mutual independent Sn<sub>4</sub>Ni<sub>3</sub> nanoparticles is presented.
As-fabricated Sn<sub>4</sub>Ni<sub>3</sub> nanoparticles deliver a
high reversible capacity of 388.9 mAh g<sup>–1</sup> at a current
density of 50 mA g<sup>–1</sup>. Especially, such materials
possess admirable cycling stability (no capacity fading after 1200
cycles at 200 mA g<sup>–1</sup>) which can be attributed to
the mutual independence of each nanoparticle. Combining with the high
rate capability, the Sn<sub>4</sub>Ni<sub>3</sub> nanoparticles present
a promising future of long-life tin-based intermetallic LIB anodes
Superconducting Continuous Graphene Fibers <i>via</i> Calcium Intercalation
Superconductors are important materials
in the field of low-temperature magnet applications and long-distance
electrical power transmission systems. Besides metal-based superconducting
materials, carbon-based superconductors have attracted considerable
attention in recent years. Up to now, five allotropes of carbon, including
diamond, graphite, C<sub>60</sub>, CNTs, and graphene, have been reported
to show superconducting behavior. However, most of the carbon-based
superconductors are limited to small size and discontinuous phases,
which inevitably hinders further application in macroscopic form.
Therefore, it raises a question of whether continuously carbon-based
superconducting wires could be accessed, which is of vital importance
from viewpoints of fundamental research and practical application.
Here, inspired by superconducting graphene, we successfully fabricated
flexible graphene-based superconducting fibers <i>via</i> a well-established calcium (Ca) intercalation strategy. The resultant
Ca-intercalated graphene fiber (Ca-GF) shows a superconducting transition
at ∼11 K, which is almost 2 orders of magnitude higher than
that of early reported alkali metal intercalated graphite and comparable
to that of commercial superconducting NbTi wire. The combination of
lightness and easy scalability makes Ca-GF highly promising as a lightweight
superconducting wire
Highly Sensitive Wearable Pressure Sensors Based on Three-Scale Nested Wrinkling Microstructures of Polypyrrole Films
Pressure sensors
have a variety of applications including wearable
devices and electronic skins. To satisfy the practical applications,
pressure sensors with a high sensitivity, a low detection limit, and
a low-cost preparation are extremely needed. Herein, we fabricate
highly sensitive pressure sensors based on hierarchically patterned
polypyrrole (PPy) films, which are composed of three-scale nested
surface wrinkling microstructures through a simple process. Namely,
double-scale nested wrinkles are generated via in situ self-wrinkling
during oxidative polymerization growth of PPy film on an elastic polyÂ(dimethylsiloxane)
substrate in the mixed acidic solution. Subsequent heating/cooling
processing induces the third surface wrinkling and thus the controlled
formation of three-scale nested wrinkling microstructures. The multiscale
nested microstructures combined with stimulus-responsive characteristic
and self-adaptive ability of wrinkling morphologies in PPy films offer
the as-fabricated piezoresistive pressure sensors with a high sensitivity
(19.32 kPa<sup>–1</sup>), a low detection limit (1 Pa), an
ultrafast response (20 ms), and excellent durability and stability
(more than 1000 circles), these comprehensive sensing properties being
higher than the reported results in literature. Moreover, the pressure
sensors have been successfully applied in the wearable electronic
fields (e.g., pulse detection and voice recognition) and microcircuit
controlling, as demonstrated here
Highly Sensitive Wearable Pressure Sensors Based on Three-Scale Nested Wrinkling Microstructures of Polypyrrole Films
Pressure sensors
have a variety of applications including wearable
devices and electronic skins. To satisfy the practical applications,
pressure sensors with a high sensitivity, a low detection limit, and
a low-cost preparation are extremely needed. Herein, we fabricate
highly sensitive pressure sensors based on hierarchically patterned
polypyrrole (PPy) films, which are composed of three-scale nested
surface wrinkling microstructures through a simple process. Namely,
double-scale nested wrinkles are generated via in situ self-wrinkling
during oxidative polymerization growth of PPy film on an elastic polyÂ(dimethylsiloxane)
substrate in the mixed acidic solution. Subsequent heating/cooling
processing induces the third surface wrinkling and thus the controlled
formation of three-scale nested wrinkling microstructures. The multiscale
nested microstructures combined with stimulus-responsive characteristic
and self-adaptive ability of wrinkling morphologies in PPy films offer
the as-fabricated piezoresistive pressure sensors with a high sensitivity
(19.32 kPa<sup>–1</sup>), a low detection limit (1 Pa), an
ultrafast response (20 ms), and excellent durability and stability
(more than 1000 circles), these comprehensive sensing properties being
higher than the reported results in literature. Moreover, the pressure
sensors have been successfully applied in the wearable electronic
fields (e.g., pulse detection and voice recognition) and microcircuit
controlling, as demonstrated here
Unique Reversible Conversion-Type Mechanism Enhanced Cathode Performance in Amorphous Molybdenum Polysulfide
A unique
reversible conversion-type mechanism is reported in the amorphous
molybdenum polysulfide (a-MoS<sub>5.7</sub>) cathode material. The
lithiation products of metallic Mo and Li<sub>2</sub>S<sub>2</sub> rather than Mo and Li<sub>2</sub>S species have been detected. This
process could yield a high discharge capacity of 746 mAh g<sup>–1</sup>. Characterizations of the recovered molybdenum polysulfide after
the delithiaiton process manifests the high reversibility of the unique
conversion reaction, in contrast with the general irreversibility
of the conventional conversion-type mechanism. As a result, the a-MoS<sub>5.7</sub> electrodes deliver high cycling stability with an energy-density
retention of 1166 Wh kg<sup>–1</sup> after 100 cycles. These
results provide a novel model for the design of high-capacity and
long-life electrode materials
Atom-Thin SnS<sub>2–<i>x</i></sub>Se<sub><i>x</i></sub> with Adjustable Compositions by Direct Liquid Exfoliation from Single Crystals
Two-dimensional (2D) chalcogenide
materials are fundamentally and
technologically fascinating for their suitable band gap energy and
carrier type relevant to their adjustable composition, structure,
and dimensionality. Here, we demonstrate the exfoliation of single-crystal
SnS<sub>2–<i>x</i></sub>Se<sub><i>x</i></sub> (SSS) with S/Se vacancies into an atom-thin layer by simple
sonication in ethanol without additive. The introduction of vacancies
at the S/Se site, the conflicting atomic radius of sulfur in selenium
layers, and easy incorporation with an ethanol molecule lead to high
ion accessibility; therefore, atom-thin SSS flakes can be effectively
prepared by exfoliating the single crystal <i>via</i> sonication.
The <i>in situ</i> pyrolysis of such materials can further
adjust their compositions, representing tunable activation energy,
band gap, and also tunable response to analytes of such materials.
As the most basic and crucial step of the 2D material field, the successful
synthesis of an uncontaminated and atom-thin sample will further push
ahead the large-scale applications of 2D materials, including, but
not limited to, electronics, sensing, catalysis, and energy storage
fields