Facile Synthesis of Biocarbon-Based MoS2 Composite for High-Performance Supercapacitor Application.

Nanocomposites are gaining high demand for the development of next-generation energy storage devices because of their eco-friendly and cost-effective natures. However, their short-term energy retainability and marginal stability are regarded as hindrances to overcome. In this work, we demonstrate a high-performance supercapacitor fabricated by biocarbon-based MoS2 (Bio-C/MoS2) nanoparticles synthesized by a facile hydrothermal approach using date fruits. Here, we report the high specific capacitance for a carbon-based nanocomposite employing the pyrolysis technique of converting agricultural biowaste into a highly affordable energy resource. The biocompatible Bio-C/MoS2 nanospheres exhibited a high capacitance of 945 F g-1 at a current density of 0.5 A g-1 and an excellent reproducing stability of 92% after 10000 charge/discharge cycles. In addition, the Bio-C/MoS2 NS showed an exceptional power density of 3800-8000 W kg-1 and an energy density of 74.9-157 Wh kg-1. The results would pave a new strategy for design of eco-friendly materials toward the high-performance energy storage technology.

FeNP@MIL-101(Fe)-Based Carbon Nanotube Composite for Energy Storage Applications.

Metal-organic frameworks (MOFs) are of great interest for energy applications due to their high porosity, high charge storage capacity, and large number of active redox sites. It is important to enhance the performance of metal-organic frameworks through modification in order to increase their potential applications. Unique Fe nanoparticle (NP) in the Materials of Institute Lavoisier (MIL) series embedded in the carbon nanotube (CNT), FeNP@MIL-101(Fe)/CNT-based, nanocomposites have been synthesized using suitable hierarchical micromesoporous structures. These were fabricated by simple and straightforward solvothermal methods, and their electrochemical charge storage performance was investigated. The energy storage application using the FeNP@MIL -101(Fe)/CNT composite as a supercapacitor electrode was implemented for the first time. Various techniques were used to characterize this composite. It has excellent electrochemical properties when used as electrode material in 1 M KOH solution, including a high capacitance of up to 1305 F g-1 at 1 A g-1 and a long cycling stability of 95.7% capacitance retention after 10,000 cycles. Moreover, symmetric two-electrode electrochemical experiments showed that the composite achieved an energy density of 98.65 Wh kg-1 and a power density of 9000 W kg-1, The combination of microporous and mesoporous structures, increased surface area, and higher electrical conductivity are the main reasons for the high performance. The integration of FeNP@MIL-101(Fe) with the CNT creates new ion diffusion pathways, improves the hierarchical pore properties, and exposes the FeNP@MIL-101(Fe) cluster to more redox active sites, which improves the charge storage performance.

Novel Au nanorod/Cu2O composite nanoparticles for a high-performance supercapacitor.

Metal-oxide nanomaterials have attracted great interest in recent years due to their novel characteristics such as surface effect and quantum confinement. A fascinating Au nanorod (NR)/cuprous oxide core-shell composite (AuNR/Cu2O) was directly synthesized using a moderate one-pot facile green redox method and further utilized for energy storage applications in a supercapacitor. The synthesis mechanism is based on the use of reducing agents to form the core shell. The resultant composite was deposited on the surface of nickel foam as a result of redox reactions between Au and Cu via a hydrothermal method. AuNR/Cu2O composite nanoparticles (NPs) were characterized using various spectroscopic and microscopic techniques, including UV-vis and X-ray photoelectron spectroscopies, Brunauer-Emmett-Teller surface area analysis, X-ray diffractometry, and transmission electron microscopy. The AuNR/Cu2O composite NPs grow via the depositing of a 20-50 nm Cu2O shell on an AuNR core with dimensions of 5-20 nm in width and 40-70 nm in length. The as-synthesized AuNR/Cu2O composite NPs were effectively used as electrode materials in a supercapacitor, and their electrochemical performance was determined by cyclic voltammetry, galvanostatic charge-discharge measurements, and electrochemical impedance spectroscopy in 2 M KOH aqueous solution as an electrolyte. The composite NPs showed excellent average specific capacitance of 235 F g-1 at a current density of 2 A g-1 and durable cycling stability (96% even after 10 000 cycles). The higher efficiency of the AuNR/Cu2O composite NPs can be attributed to the presence of AuNR in the core. The AuNR/Cu2O composite NPs exhibit a high surface area and high electrical conductivity, which consequently result in their excellent specific capacitance and outstanding rate as an all-solid-state supercapacitor electrode.

Well-Designed Au Nanorod-Doped Cu2O Core-Shell Nanocube-Embedded Reduced Graphene Oxide Composite for Efficient Removal of a Water Pollutant Dye.

To ensure environmental safety, the removal of organic pollutants has gained increasing attention globally. We have synthesized uniform Au nanorod (NR)-doped Cu2O core-shell nanocubes (CSNCs) via a seed-mediated route embedded on the surface of rGO sheets. The Au NRs@Cu2O/rGO nanocomposite was characterized using various techniques such as transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier-transform infrared (FT-IR) and Raman spectroscopies. The scanning TEM-energy-dispersive spectroscopy (STEM-EDS) elemental mapping of the AuNRs@Cu2O/rGO nanocomposite indicates that the Au NR (40 nm) is fully covered with the Cu2O particles (∼145 nm) as a shell. N2 gas sorption analysis shows that the specific surface area of the composite is 205.5 m2/g with a mesoporous character. Moreover, incorporation of Au NRs@Cu2O CSNCs increases the nanogaps around the nanoparticles and suppresses the stacking/bundling of rGO, which significantly influences the pore size and increase the surface area. A batch adsorption experiment was carried out under various parameters, such as the effect of pH, contact time, temperature, initial dye concentration, and adsorbent dosage, for the removal of methylene blue (MB) in aqueous solution. The high surface area and mesoporosity can cause the adsorption capacity to reach equilibrium within 20 min with a 99.8% removal efficiency. Both kinetic and isotherm data were obtained and fitted very well with the pseudo-second-order kinetic and Langmuir isotherm model. The Langmuir isotherm revealed an excellent dye sorption capacity of 243.9 mg/g at 298 K. Moreover, after five adsorption cycles, the dye removal efficiency decreased from 99 to 86%. This novel route paves a new path for heterogeneous adsorbent synthesis, which is useful for catalysis and electrochemical applications.