Extrinsic Pseudocapacitive NiSe/rGO/g-C3N4 Nanocomposite for High-Performance Hybrid Supercapacitors.

Battery-type materials with ultrahigh energy density show great potential for hybrid supercapacitors (HSCs). In this work, we have developed a nickel selenide (NiSe)/reduced graphene oxide (rGO)/graphitic carbon nitride (g-C3N4) ternary composite as a promising positive electrode for hybrid supercapacitors (HSCs). The extended π-conjugated planar layers of g-C3N4 promote strong interconnectivity with rGO, which further enhances surface area, surface free energy, and efficient electron/ionic path. Additionally, it establishes clear ion diffusion pathways, serving as ion reservoirs during charge and discharge and facilitating efficient redox reactions. As a result, the NiSe/g-C3N4/rGO nanocomposite electrode displayed a specific capacity of 412.6 mA h g-1 at 1 A g-1. Later, the HSC device was assembled using the nanocomposite as the positive electrode and activated carbon as the negative electrode, which delivered an energy density of 65.2 Wh kg-1 at a power density of 750 W kg-1. Notably, the HSC device maintained excellent cyclic stability, preserving 93.3% of its initial performance and Coulombic efficiency of 86.6% for 10,000 charge-discharge cycles at 5 A g-1. These findings underscore the potential utility of NiSe/g-C3N4/rGO as a versatile and effective electrode material for the strategic development of HSC devices.

Core-Shell Structured MXene@Carbon Nanodots as Bifunctional Catalysts for Solar-Assisted Water Splitting.

The design of nonprecious bifunctional electrocatalysts with high activity and prolonged durability in a wide pH range is essential for the development of the highly efficient, cost-effective, and simplified overall water splitting systems. Here, we report core-shell structured MXene@carbon (MX@C) nanodot hybrids with high bifunctional activity, where N-doped carbon shells are grown in a heteroepitaxial manner strongly interacting with the MXene core. The resulting MX@C nanodot hybrids show enhanced catalytic activity for electrochemical hydrogen evolution reaction (HER) in various pH media from 0 to 14. At pH 14, MX@C achieves the low onset potential of 134 mV at 10 mA/cm2 and reduced Tafel slope of 32 mV/dec due to the facilitated charge transfer along the recombination reaction. For the oxygen evolution reaction (OER), MX@C nanodots are incorporated onto the surface of molybdenum-doped bismuth vanadate (Mo:BiVO4) as a cocatalyst of the photoanode, thereby achieving 1.5 times higher photocurrent density than pristine Mo:BiVO4 at 1.23 V (vs reversible hydrogen electrode) due to the enhanced light absorption and charge transfer efficiency. The superiority of this hybrid catalyst is demonstrated implementing the solar-assisted overall water splitting cells based on the MX@C cathode and MX@C/Mo:BiVO4 photoanode. These cells show the enhancement of current density from 0.78 to 1.23 mA/cm2 with long-term durability over 8 h. These results are attributed to the facile surface catalytic kinetics of the chemically and electronically coupled MX@C hybrid at the heterointerface for both OER and HER.

Two-Dimensional Metallic Niobium Diselenide for Sub-micrometer-Thin Antennas in Wireless Communication Systems.

The state-of-the-art of the Internet of things (IoT) and smart electronics demands advances in thin and flexible radio frequency (RF) antennas for wireless communication systems. So far, nanostructured materials such as metals, carbon nanotubes, graphene, MXene, and conducting polymers have been investigated due to their noteworthy electrical conductivity. However, most antennas based on metallic materials are thick, which limits their application in miniaturized and portable electronic devices. Herein, we report two-dimensional (2D) metallic niobium diselenide (NbSe2) for a monopole patch RF antenna, which functions effectively despite its sub-micrometer thickness, which is less than the skin depths of other metals. The as-fabricated antenna has an 855 nm thickness and a 1.2 Ω sq-1 sheet resistance and achieves a reflection coefficient of -46.5 dB, a radiation efficiency of 70.6%, and omnidirectional RF propagation. Additionally, the resonance frequency of this antenna at the same thickness is reconfigured from 2.01 to 2.80 GHz, while decreasing its length and preserving its reflection coefficient of less than -10 dB. This approach offers a facile process to synthesize 2D metallic transition metal dichalcogenides for the rational design of flexible, miniaturized, frequency-tunable, and omnidirectional monopole patch RF antennas for body-centric wearable communication systems.

Low-cost flexible supercapacitors with high-energy density based on nanostructured MnO2 and Fe2O3 thin films directly fabricated onto stainless steel.

The facile and economical electrochemical and successive ionic layer adsorption and reaction (SILAR) methods have been employed in order to prepare manganese oxide (MnO2) and iron oxide (Fe2O3) thin films, respectively with the fine optimized nanostructures on highly flexible stainless steel sheet. The symmetric and asymmetric flexible-solid-state supercapacitors (FSS-SCs) of nanostructured (nanosheets for MnO2 and nanoparticles for Fe2O3) electrodes with Na2SO4/Carboxymethyl cellulose (CMC) gel as a separator and electrolyte were assembled. MnO2 as positive and negative electrodes were used to fabricate symmetric SC, while the asymmetric SC was assembled by employing MnO2 as positive and Fe2O3 as negative electrode. Furthermore, the electrochemical features of symmetric and asymmetric SCs are systematically investigated. The results verify that the fabricated symmetric and asymmetric FSS-SCs present excellent reversibility (within the voltage window of 0-1 V and 0-2 V, respectively) and good cycling stability (83 and 91%, respectively for 3000 of CV cycles). Additionally, the asymmetric SC shows maximum specific capacitance of 92 Fg(-1), about 2-fold of higher energy density (41.8 Wh kg(-1)) than symmetric SC and excellent mechanical flexibility. Furthermore, the "real-life" demonstration of fabricated SCs to the panel of SUK confirms that asymmetric SC has 2-fold higher energy density compare to symmetric SC.

Architectured morphologies of chemically prepared NiO/MWCNTs nanohybrid thin films for high performance supercapacitors.

The preparation of nanostructured metal oxide decorated on multiwalled carbon nanotubes (MWCNTs) nanohybrid films through simple, scalable, additive-free, binderless, and cost-effective route has fascinated significant attention not only in fundamental research areas but also its commercial applications, in order to reduce the growing environmental pollution and the cost of electrode fabrication. Here, we report the fabrication of highly flexible electrode with NiO/MWCNTs nanohybrid thin films directly on stainless steel substrate using successive ionic layer adsorption and reaction (SILAR) method. The impact of ratio of adsorption and reaction cycles on structural, surface areas and electrochemical properties of NiO/MWCNTs nanohybrids was investigated. X-ray diffraction measurements confirm the hybridization and face centered cubic (FCC) crystal structure of NiO in NiO/MWCNTs nanohybrids. In addition, these nanohybrids exhibit excellent surface properties such as uniform surface morphology, good surface area, pore volume, and uniform pore size distribution. The electrochemical tests demonstrate the highest specific capacitance of 1727 F g(-1) at 5 mA cm(-2) of current density with 91% capacitance retention after 2000 cycles. In addition, the Ragone plot confirms the better power and energy densities for all NiO/MWCNTs nanohybrids. The attractive electrochemical capacitive activity revealed by NiO/MWCNTs nanohybrid electrode proposes that it is an auspicious respondent for future energy storage application.

Surfactant-assisted morphological tuning of hierarchical CuO thin films for electrochemical supercapacitors.

Copper oxide (CuO) thin films are successfully synthesized using a surfactant assisted chemical bath deposition method for application in supercapacitors. The effect of organic surfactants such as Triton X-100 and polyvinyl alcohol (PVA) on structural, morphological, surface areas and electrochemical properties of CuO thin films is investigated. The films deposited using organic surfactants exhibit different surface morphologies. It is observed that the organic surfactants play important roles in modifying the morphology, surface area and pore size distribution. Electrochemical analysis confirms that the nanostructures of the electrode material play a vital role in supercapacitors. The cyclic voltammetry studies show a considerably improved high rate pseudocapacitance of CuO samples synthesized using organic surfactants. The maximum specific capacitance of 411 F g(-1) at 5 mV s(-1) is obtained for the CuO sample prepared using an organic surfactant (Triton X-100). Furthermore, all the CuO nanostructures exhibit high power performance, excellent rate as well as long term cycling stability. The Ragone plot ascertains better power and energy densities of CuO nanostructured samples. This is an easy and simple way to tune the morphology using surfactants which can be applied for other energy storage materials.

Decoration of spongelike Ni(OH)2 nanoparticles onto MWCNTs using an easily manipulated chemical protocol for supercapacitors.

This study uses a "bottom-up" approach chemical method to coat nanocrystalline Ni(OH)2 onto multiwalled carbon nanotubes (MWCNTs) for flexible supercapacitor electrodes, where the higher electronic conductivity of MWCNTs permits their use as the supporting backbone onto which Ni(OH)2 can be deposited. The paper portrays the advantages of the facile successive ionic layer adsorption and reaction (SILAR) method for depositing Ni(OH)2/MWCNT thin films onto large area flexible substrates. We demonstrate that these Ni(OH)2/MWCNT films consist of a uniform coating of sponge-like Ni(OH)2 on the MWCNT network structure using scanning electron micrographs and transmission electron micrographs; this structure is promising for supercapacitor applications. Ni(OH)2/MWCNT films exhibit a specific capacitance of 1487 F g(-1) at a scan rate of 5 mV s(-1) in a 2 M KOH aqueous solution. The electrodes are generated using a simple three-beaker SILAR system at ambient conditions, thus providing an easy approach to fabricate high-power and high-energy flexible supercapacitors. Ni(OH)2/MWCNTs demonstrate a good rate capability and excellent long-term cyclic stability (96% capacity retention after 1000 cycles). Such high-performance capacitive behavior indicates that Ni(OH)2/MWCNT composites are promising electrode materials for the fabrication of supercapacitors. Thus, the method described in this paper provides a generalized route for the production of a wide range of Ni(OH)2/MWCNT-based materials for applications beyond electrochemical energy storage. These encouraging results promote interest in developing such devices, including nontoxic and greener components, compared with current organic-based devices.