Boron vacancy: a strategy to boost the oxygen reduction reaction of hexagonal boron nitride nanosheet in hBN-MoS2 heterostructure.

The incorporation of vacancies in a system is considered a proficient method of defect engineering in general catalytic modulation. Among two-dimensional materials, the deficiency of surface active sites and a high band gap restrict the catalytic activity of hexagonal boron nitride (hBN) material towards the oxygen reduction reaction (ORR), which hinders its applicability in fuel cells. A bane to boon strategy has been introduced here by coupling two sluggish ORR materials (hBN & MoS2) by a probe-sonication method to form a heterostructure (termed HBPS) which fosters four electron pathways to assist the reduction of oxygen. Theoretical and experimental studies suggest the kinetically and thermodynamically favorable formation of boron vacancies (B-vacancies) in the presence of MoS2, which act as active sites for oxygen adsorption in HBPS. B-vacancy induced uneven charge distribution together with band gap depression promote rapid electron transfer from the valance band to the conduction band which prevails over the kinetic limitation of pure hBN nanosheets towards ORR kinetics. The formed B-vacancy induced HBPS further exhibits a low Tafel slope (66 mV dec-1), and a high onset potential (0.80 V vs. RHE) with an unaltered electrochemically active surface area (ESCA) after long-term cycling. Thus, vacancy engineering in hBN has proved to be an efficient approach to unlock the potential of catalytic performance enhancement.

Investigation of ORR Performances on Graphene/Phthalocyanine Nanocomposite in Neutral Medium.

The drive to replace scarce and expensive Pt-based electrocatalysts for oxygen reduction reaction (ORR) has led to the development of a group of electrocatalysts composed of transition-metal ion centers coordinated with four nitrogen groups (M-N4). Among these, metal phthalocyanines (MPcs), due to low cost of preparation, highly conjugated structure as well as high thermal and chemical stability, have received a great interest. The catalytic activity of MPcs can be improved by employing conducting supports. Here, in this report, we have solvothermally synthesized graphene-supported zinc phthalocyanine nanostructures, and their ORR kinetics and mechanism have been investigated in neutral solution (pH = 7) by using the rotating disk electrode technique. The as-synthesized nanocomposite followed a 4e- reduction pathway. The onset potential (-0.04 V versus Ag/AgCl) found in this work can be comparable with other state-of-the-art material, demonstrating good performance in neutral solution. The fascinating performance leads the nanocomposite material toward future energy applications.

Band edge tuned ZnxCd1-xS solid solution nanopowders for efficient solar photocatalysis.

This work highlights the synthesis of zinc blende ZnxCd1-xS ternary solid solutions with a tunable bandgap. Composition dependent band gaps are realized due to the effective band edge tuning of the solid solutions which in turn show decent photocatalytic behaviour. The bandgap of ZnxCd1-xS increases as Zn composition increases. It is interesting to note that the highest catalytic activity is observed for Zn0.8Cd0.2S (Eg = 2.83 eV) in the visible spectra due to the presence of defect states in the bandgap around 2.35 eV which has been explicated according to the results of photoluminescence spectra. Density of states (DOS) analysis provides further theoretical insight into the more negative conduction band edge for x = 0.8 than other samples. It also determines generation of intermediate states due to sulfur vacancy which is responsible for more electron-hole generation and the highest rate of Methyl Orange (MO) degradation under natural sunlight irradiation.

Novel Quaternary Chalcogenide/Reduced Graphene Oxide-Based Asymmetric Supercapacitor with High Energy Density.

In this work we have synthesized quaternary chalcogenide Cu2NiSnS4 (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-2), which is much superior to that of commercial micro-supercapacitors. Furthermore, a remarkable volumetric capacitance of 16.38 F cm-3 is obtained at a current density of 5 mA cm-2 combined with a very high energy density of 5.68 mW h cm-3, 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, Cu2NiSnS4 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.

Co3O4 Nanowires on Flexible Carbon Fabric as a Binder-Free Electrode for All Solid-State Symmetric Supercapacitor.

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 Co3O4 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 Co3O4 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.