Since the successful synthesis of the first MXenes, application developments of this new family of two-dimensional materials on energy storage, electromagnetic interference shielding, transparent conductive electrodes and field-effect transistors, and other applications have been widely reported. However, no one has found or used the basic characteristics of greatly changed interlayer distances of MXene under an external pressure for a real application. Here we report a highly flexible and sensitive piezoresistive sensor based on this essential characteristics. An in situ transmission electron microscopy study directly illustrates the characteristics of greatly changed interlayer distances under an external pressure, supplying the basic working mechanism for the piezoresistive sensor. The resultant device also shows high sensitivity (Gauge Factor ~ 180.1), fast response (<30 ms) and extraordinarily reversible compressibility. The MXene-based piezoresistive sensor can detect human being’s subtle bending-release activities and other weak pressure.
In large-scale applications of portable and wearable electronic devices, high-performance supercapacitors are important energy supply sources. However, since the reliability and stability of supercapacitors are generally destroyed by mechanical deformation and damage during practical applications, the stretchability and self-healability must be exploited for the supercapacitors. Preparing the highly stretchable and self-healable electrodes is still a challenge. Here, we report reduced graphene oxide fiber based springs as electrodes for stretchable and self-healable supercapacitors. The fiber springs (diameters of 295 μm) are thick enough to reconnect the broken electrodes accurately by visual inspection. By wrapping fiber springs with a self-healing polymer outer shell, a stretchable and self-healable supercapacitor is successfully realized. The supercapacitor has 82.4% capacitance retention after a large stretch (100%), and 54.2% capacitance retention after the third healing. This work gave an essential strategy for designing and fabricating stretchable and self-healable supercapacitors in next-generation multifunctional electronic devices.
Nowadays, the integrated systems on a plane substrate containing energy harvesting, energy storing, and working units are strongly desired with the fast development of wearable and portable devices. Here, a simple, low cost, and scalable strategy involving ink printing and electrochemical deposition is proposed to fabricate a flexible integrated system on a plane substrate containing an all-solid-state asymmetric microsupercapacitor (MSC), a photoconduct-type photodetector of perovskite nanowires (NWs), and a wireless charging coil. In the asymmetric MSCs, MnO-PPy and VO-PANI composites are used as positive and negative electrodes, respectively. Typical values of energy density in the range of 15-20 mWh cm at power densities of 0.3-2.5 W cm with an operation potential window of 1.6 V are achieved. In the system, the wireless charging coil receives energy from a wireless power transmitter, which then can be stored in the MSC to drive the photoconductive detector of perovskite NWs in sequence. The designed integrated system exhibits a stable photocurrent response comparable with the detector driven by an external power source. This research provides an important routine to fabricate integrated systems.
Ultra-thin W(18)O(49) nanowires were initially obtained by a simple solvothermal method using tungsten chloride and cyclohexanol as precursors. Thermal processing of the resulting bundled nanowires has been carried out in air in a tube furnace. The morphology and phase transformation behavior of the as-synthesized nanowires as a function of annealing temperature have been characterized by x-ray diffraction and electron microscopy. The nanostructured bundles underwent a series of morphological evolution with increased annealing temperature, becoming straighter, larger in diameter, and smaller in aspect ratio, eventually becoming irregular particles with size up to 5 µm. At 500 °C, the monoclinic W(18)O(49) was completely transformed to monoclinic WO(3) phase, which remains stable at high processing temperature. After thermal processing at 400 °C and 450 °C, the specific surface areas of the resulting nanowires dropped to 110 m(2) g(-1) and 66 m(2) g(-1) respectively, compared with that of 151 m(2) g(-1) for the as-prepared sample. This study may shed light on the understanding of the geometrical and structural evolution occurring in nanowires whose working environment may involve severe temperature variations.
Exploring
nanostructured transition-metal sulfide anode materials
with excellent electrical conductivity is the key point for high-performance
alkali metal ion storage devices. Herein, we propose a powerful bottom-up
strategy for the construction of a series of sandwich-structured materials
by a rapid interfacial self-assembly approach. Oleylamine could act
as a functional reagent to guarantee that the nanomaterials self-assemble
with MXene. Benefiting from the small size of Co-NiS nanorods, excellent
conductivity of MXene, and sandwiched structure of the composite,
the Co-NiS/MXene composite could deliver a high discharge capacity
of 911 mAh g–1 at 0.1 A g–1 for
lithium-ion storage. After 200 cycles at 0.1 A g–1, a high specific capacity of 1120 mAh g–1 could
be still remaining, indicating excellent cycling stability. For sodium-ion
storage, the composite exhibits high specific capacity of 541 mAh
g–1 at 0.1 A g–1 and excellent
rate capability (263 mAh g–1 at 5 A g–1). This work offers a straightforward strategy to design and construct
MXene-based anode nanomaterials with sandwiched structure for high-performance
alkali metal ion storage and even in other fields.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.