No abstract

A strong nonlinear optical response of 2D MoSe2 nanoflakes (NFs) through spatial self‐phase modulation (SSPM) and cross‐phase modulation (XPM) induced by nonlocal coherent light–matter interactions is reported. The coherent interaction of light and MoSe2 NFs creates the SSPM of laser beams, forming concentric diffraction rings. The nonlinear refractive index (n2) and third‐order broadband nonlinear optical susceptibility (χ(3)) of MoSe2 NFs are determined from the self‐diffraction pattern at different exciting wavelengths of 405, 532, and 671 nm with varying laser intensity. The evolution and deformation of diffraction ring patterns are observed and analyzed by the “wind‐chime” model and thermal effect. By taking advantage of the reverse saturated absorption of 2D SnS2 NFs compared to MoSe2, an all‐optical diode has been designed with MoSe2/SnS2 hybrid structure to demonstrate the nonreciprocal light propagation. Few other optical devices based on MoSe2 and semiconducting materials such as Bi2Se3, CuPc, and graphene have been investigated. The all‐optical logic gates and all‐optical information conversion have been demonstrated through the XPM technique using two laser beams. The proposed optical scheme based on MoSe2 NFs has been demonstrated as a potential candidate for all‐optical nonlinear photonic devices such as all‐optical diodes and all‐optical switches.

In this work we have synthesized quaternary chalcogenide CuNiSnS (QC) nanoparticles grown in situ on 2D reduced graphene oxide (rGO) for application as anode material of solid-state asymmetric supercapacitors (ASCs). Thorough characterization of the synthesized composite validates the proper phase, stoichiometry, and morphology. Detailed electrochemical study of the electrode materials and ASCs has been performed. The as-fabricated device delivers an exceptionally high areal capacitance (655.1 mF cm), which is much superior to that of commercial micro-supercapacitors. Furthermore, a remarkable volumetric capacitance of 16.38 F cm is obtained at a current density of 5 mA cm combined with a very high energy density of 5.68 mW h cm, which is comparable to that of commercially available lithium thin film batteries. The device retains 89.2% of the initial capacitance after running for 2000 cycles, suggesting its long-term capability. Consequently, the enhanced areal and volumetric capacitances combined with decent cycle stability and impressive energy density endow the uniquely decorated QC/rGO composite material as a promising candidate in the arena of energy storage devices. Moreover, CuNiSnS being a narrow band gap photovoltaic material, this work offers a novel protocol for the development of self-charging supercapacitors in the days to come.

Developing portable, lightweight, and flexible energy storage systems has become a necessity with the advent of wearable electronic devices in our modern society. This work focuses on the fabrication of Co 3 O 4 nanowires on a flexible carbon fabric (CoNW/CF) substrate by a simple cost-effective hydrothermal route. The merits of the high surface area of the prepared Co 3 O 4 nanostructures result in an exceptionally high specific capacitance of 3290 F/g at a scan rate of 5 mV/s, which is close to their theoretical specific capacitance. Furthermore, a solid-state symmetric supercapacitor (SSC) based on CoNW/CF (CoNW/CF//CoNW/CF) was fabricated successfully. The device attains high energy and power densities of 6.7 Wh/kg and 5000 W/kg. It also demonstrates excellent rate capability and retains 95.3% of its initial capacitance after 5000 cycles. Further, the SSC holds its excellent performance at severe bending conditions. When a series assembly of four such devices is charged, it can store sufficient energy to power a series combination of five light-emitting diodes. Thus, this SSC device based on a three-dimensional coaxial architecture opens up new strategies for the design of next-generation flexible supercapacitors.

No abstract

No abstract

No abstract

Fabrication of noble-metal-free, earth-abundant, inexpensive, and efficient electrocatalyst for hydrogen evolution reaction (HER) is a challenge for clean and sustainable energy carrier. Transition-metal dichalcogenides have shown their potential as an electrode material toward electrochemical HER activity. Herein we successfully developed hierarchical core–shell nanostructure of molybdenum diselenide (MoSe2)-amorphous carbon nanotube (aCNT) via a simple solvothermal procedure, showing excellent electrocatalytic HER activity in acidic medium. The MoSe2-aCNT exhibits onset potential as low as −64 mV and small Tafel slope of ∼49 mV/dec with an HER activity superior to that of the pristine aCNTs and MoSe2. Experimental results along with theoretical investigation demonstrate that the exposed active edges of MoSe2 nanosheet on amorphous wall of the aCNTs with a low free energy barrier promote the improvement of electrocatalytic HER activity. This work opens a new strategy for the development of advanced amorphous carbon nanostructure-based hybrid HER catalyst in acidic medium.