Embedding Cobalt Atom Clusters in CNT-Wired MoS2 Tube-in-Tube Nanostructures with Enhanced Sulfur Immobilization and Catalyzation for Li-S Batteries.

Lithium-sulfur batteries are one of the most promising next-generation energy storage systems. The efficient interconversion between sulfur/lithium polysulfides and lithium sulfide is a performance-determining factor for lithium-sulfur batteries. Herein, a novel strategy to synthesize a unique tube-in-tube CNT-wired sulfur-deficient MoS2 nanostructure embedding cobalt atom clusters as an efficient polysulfide regulator is successfully conducted in Li-S batteries. It is confirmed that encapsulating MWCNTs into hollow porous sulfur-deficient MoS2 nanotubes embedded with metal cobalt clusters not only can accelerate electron transport and confine the dissolution of lithium polysulfide by physical/chemical adsorption, but also can catalyze the kinetics of polysulfide redox reactions. Based on DFT calculations, in situ spectroscopic techniques, and various electrochemical studies, catalytic effects of CNT/MoS2 -Co nanocomposite in Li-S battery are deeply investigated for the first time. The CNT/MoS2 -Co composite cathode exhibits a very remarkable rate capability (641 mAh g-1 at 5.0 C) and excellent cycling stability (capacity decay rate of 0.050% per cycle at 5.0 C) even at high sulfur mass loading of 3.6 mg cm-2 . More crucially, CNT/MoS2 -Co tube-in-tube nanostructures present a superior specific capacity of 650 mAh g-1 in a Li-S pouch cell at 0.2 C (4.0 mg cm-2 ).

A Review of Rechargeable Zinc-Air Batteries: Recent Progress and Future Perspectives.

Zinc-air batteries (ZABs) are gaining attention as an ideal option for various applications requiring high-capacity batteries, such as portable electronics, electric vehicles, and renewable energy storage. ZABs offer advantages such as low environmental impact, enhanced safety compared to Li-ion batteries, and cost-effectiveness due to the abundance of zinc. However, early research faced challenges due to parasitic reactions at the zinc anode and slow oxygen redox kinetics. Recent advancements in restructuring the anode, utilizing alternative electrolytes, and developing bifunctional oxygen catalysts have significantly improved ZABs. Scientists have achieved battery reversibility over thousands of cycles, introduced new electrolytes, and achieved energy efficiency records surpassing 70%. Despite these achievements, there are challenges related to lower power density, shorter lifespan, and air electrode corrosion leading to performance degradation. This review paper discusses different battery configurations, and reaction mechanisms for electrically and mechanically rechargeable ZABs, and proposes remedies to enhance overall battery performance. The paper also explores recent advancements, applications, and the future prospects of electrically/mechanically rechargeable ZABs.

Manganese cobalt sulfide/molybdenum disulfide nanowire heterojunction as an excellent bifunctional catalyst for electrochemical water splitting.

Heterointerface engineering enhances catalytic active centers and charge transfer capabilities to increase oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) kinetics. In this study, a novel heterostructure of manganese cobalt sulfide-molybdenum disulfide on nickel foam (MnCo2S4-MoS2/NF) was synthesized via a two-step hydrothermal process. The nanowire-shaped MnCo2S4-MoS2 on NF displayed accelerated charge transfer ability and multiple integrated active sites. When tested in one molar (1 M) potassium hydroxide (KOH) electrolyte, it furnished low overpotentials of 105 and 171 mV for the HER and 220 and 300 mV for the OER at the current densities of 20 and 50 mA cm-2, respectively. An electrolyzer based on MnCo2S4-MoS2/NF required low operating potentials of 1.41 and 1.49 V to yield the current densities of 10 and 20 mA cm-2, respectively, surpassing commercial and previously reported catalysts. Density functional theory (DFT) analysis revealed that the MnCo2S4-MoS2 heterostructure possesses the optimal adsorption free energies for the reactants, an extended electroactive surface area, good charge transfer ability, and reasonable density of electronic states close to the Fermi level, all of which contribute to the high activity of catalyst. Thus, heterointerface engineering is a promising strategy for creating efficient catalysts for overall water splitting.

Enhancing the electrochemical activity of zinc cobalt sulfide via heterojunction with MoS2 metal phase for overall water splitting.

The integration of diverse components into a single heterostructure represents an innovative approach that boosts the quantity and variety of active centers, thereby enhancing the catalytic activity for both hydrogen evolution reactions (HER) and oxygen evolution reactions (OER) in the water splitting process. In this study, a novel, hierarchically porous one-dimensional nanowire array comprising zinc cobalt sulfide and molybdenum disulfide (MoS2@Zn0.76Co0.24S) was successfully synthesized on a Ni foam substrate using an efficient and straightforward hydrothermal synthesis strategy. The incorporation of the metallic phase of molybdenum disulfide elevates the electronic conductivity of MoS2@Zn0.76Co0.24S, resulting in impressively low overpotentials. At 20, 50, and 100 mA cm-2, the overpotentials for oxygen evolution reaction (OER) are merely 90 mV, 170 mV, and 240 mV, respectively. Similarly, for hydrogen evolution reaction (HER), the overpotentials are 169 mV, 237 mV, and 301 mV at the same current densities in 1.0 M potassium hydroxide solution. The utilization of the MoS2@Zn0.76Co0.24S /NF electrolyzer demonstrates its exceptional performance as a catalyst in alkaline electrolyzers. Operating at a mere 1.45 V and 10 mA cm-2, it showcases outstanding efficiency. Achieving a current density of 405 mA cm-2, the system generates hydrogen at a rate of 3.1 mL/min with a purity of 99.997%, achieving an impressive cell efficiency of 68.28% and a voltage of 1.85 V. Furthermore, the MoS2@Zn0.76Co0.24S /NF hybrid exhibits seamless integration with solar cells, establishing a photovoltaic electrochemical system for comprehensive water splitting. This wireless assembly harnesses the excellent performance of the hybrid nanowire, offering a promising solution for efficient, durable, and cost-effective bifunctional electrocatalysts in the realm of renewable energy.

Rational Design of a Copper Cobalt Sulfide/Tungsten Disulfide Heterostructure for Excellent Overall Water Splitting.

Integrating different components into a heterostructure is a novel approach that increases the number of active centers to enhance the catalytic activities of a catalyst. This study uses an efficient, facile hydrothermal strategy to synthesize a unique heterostructure of copper cobalt sulfide and tungsten disulfide (CuCo2S4-WS2) nanowires on a Ni foam (NF) substrate. The nanowire arrays (CuCo2S4-WS2/NF) with multiple integrated active sites exhibit small overpotentials of 202 (299) and 240 (320) mV for HER and OER at 20 (50) mA cm-2 and 1.54 V (10 mA cm-2) for an electrolyzer in 1.0 M KOH, surpassing commercial and previously reported catalysts. A solar electrolyzer composed of CuCo2S4-WS2 bifunctional electrodes also produced significant amounts of hydrogen through a water splitting process. The remarkable performance is accredited to the extended electroactive surface area, reasonable density of states near the Fermi level, optimal adsorption free energies, and good charge transfer ability, further validating the excellent dual function of CuCo2S4-WS2/NF in electrochemical water splitting.

Three-dimensional nano assembly of nickel cobalt sulphide/polyaniline@polyoxometalate/reduced graphene oxide hybrid with superior lithium storage and electrocatalytic properties for hydrogen evolution reaction.

Engineering hierarchical nanostructures with enhanced charge storage capacity and electrochemical activity are vital for the advancement of energy devices. Herein, a highly ordered mesoporous three-dimensional (3D) nano-assembly of Nickel Cobalt Sulphide/Polyaniline @Polyoxometalate/Reduced Graphene Oxide (NiCo2S4/PANI@POM/rGO) is prepared first time via a simple route of oxidative polymerization followed by a hydrothermal method. Morphological analysis of the resulting hybrid reveals the sheet-like structures containing a homogeneous assembly of PANI@POM and NiCo2S4 on the graphene exterior maintaining huge structural integrity, large surface area and electrochemically active centres. The electrochemical analysis of the nanohybrid as the anode of the lithium-ion battery (LIB) has delivered ultra-huge reversible capacity of 735.5 mA h g-1 (0.1 A g-1 after 200 cycles), superb capacity retention (0.161% decay/per cycle at 0.5 A g-1 for 1000 cycles), and significant rate capability (355.6 mA h g-1 at 2 A g-1). The hydrogen evolution reaction (HER) measurement also proves remarkable activity, extremely low overpotential and high durability. The extraordinary performance of the nanohybrid is due to the presence of abundant electroactive centres, high surface area and a large number of ion exchange channels. These outstanding results prove the advantages of a combination of NiCo2S4, graphene sheets, and PANI@POM in energy devices.

Heterostructure of polyoxometalate/zinc-iron-oxide nanoplates as an outstanding bifunctional electrocatalyst for the hydrogen and oxygen evolution reaction.

Electrocatalysts play an important role to increase the energy conversion efficiency of electrolysis processes. In this study, a heterostructure of zinc iron oxide (ZnFe2O4) and polyoxometalate (POM) nanoplates (POM-ZnFe2O4) was fabricated for the first time by a hydrothermal process. The hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) analysis of POM-ZnFe2O4 furnished low overpotentials of 268 and 356 mV, and 220 and 290 mV to achieve current densities of 20 and 50 mA cm-2, respectively. In addition, an electrolytic cell composed of a POM-ZnFe2O4 cathode and anode required an operating voltage of 1.53 V to deliver a current of 10 mA cm-2. The improved electrochemical performance of POM-ZnFe2O4 compared to commercial and recently reported catalysts is attributed to the high electrocatalytically active surface area, modulation in the electronic and chemical properties and the formation of heterojunction of ZnFe2O4 and POM, which are vital for accelerating HER and OER activity.

Homogeneous Elongation of N-Doped CNTs over Nano-Fibrillated Hollow-Carbon-Nanofiber: Mass and Charge Balance in Asymmetric Supercapacitors Is No Longer Problematic.

The hurdle of fabricating asymmetric supercapacitor (ASC) devices using a faradic cathode and a double layer anode is challenging due to the required large amount of active mass of anodic material compared to that of the cathodic material during mass balancing due to the large difference in capacitance values of the two electrodes. Here, the problem is addressed by engineering a negative electrode that furnishes an ultrahigh capacitance. An in situ developed metal-organic framework (MOF)-based thermal treatment is adopted to grow highly porous N-doped carbon nanotubes (CNTs) containing submerged Co nanoparticles over nano-fibrillated electrospun hollow carbon nanofibers (HCNFs). The optimized CNT@HCNF-1.5 furnishes an ultrahigh capacitance approaching 712 F g-1 with excellent rate capability. The capacitance reported from this work is the highest for any carbonaceous material reported to date. The CNT@HCNF-1.5 is further used to fabricate symmetric supercapacitors (SSCs), as well as ASC devices. Remarkably, both the SSC and ASC devices furnish incredible performances in all aspects of SCs, such as a high energy density, long cycle life, and high rate capability, displaying decent practical applicability. The energy density of the SSC device reaches as high as 20.13 W h kg-1 , whereas that of ASC approaches 87.5 W h kg-1 .

Mesoporous layered spinel zinc manganese oxide nanocrystals stabilized nitrogen-doped graphene as an effective catalyst for oxygen reduction reaction.

The design of low-cost, highly efficient, and the durable catalyst is essential to replace commercial platinum metal-based catalysts for the oxygen reduction reaction (ORR) in fuel cell applications. Herein, a novel mesoporous hybrid based on nitrogen-doped graphene nanosheets-stabilized layered spinel zinc manganese oxide (Zn2Mn3O8-NG) is successfully engineered and applied as an effective catalyst to accelerate the ORR process in alkaline medium. Electrochemical performance analysis of this catalyst shows excellent catalytic activity with high current density, positive onset potential (-0.013 V), and positive half-wave potential (-0.12 V), which are relative to the commercial Pt/C in 0.1 M KOH electrolyte. The kinetic study of the synthesized catalyst towards ORR demonstrates a direct 4e- transfer pathway. The methanol tolerance and long-term stability test suggest its superior behavior to Pt/C. The excellent performance of the Zn2Mn3O8-NG is attributed to the synergistic effects of nanosized Zn2Mn3O8 nanocrystals and NG nanosheets, which effectively improve the electroactive surface area, conductivity, diffusion channels, and mass transfer ability. This result suggests that the resulting catalyst could be used as a potential alternative of Pt-based catalysts towards ORR application.

Hierarchical Flowerlike Highly Synergistic Three-Dimensional Iron Tungsten Oxide Nanostructure-Anchored Nitrogen-Doped Graphene as an Efficient and Durable Electrocatalyst for Oxygen Reduction Reaction.

A unique and novel structural morphology with high specific surface area, highly synergistic, remarkable porous conductive networks with outstanding catalytic performance, and durability of oxygen reduction electrocatalyst are typical promising properties in fuel cell application; however, exploring and interpreting this fundamental topic is still a challenging task in the whole world. Herein, we have demonstrated a simple and inexpensive synthesis strategy to design three-dimensional (3D) iron tungsten oxide nanoflower-anchored nitrogen-doped graphene (3D Fe-WO3 NF/NG) hybrid for a highly efficient synergistic catalyst for oxygen reduction reaction (ORR). The construction of flowerlike Fe-WO3 nanostructures, based on synthesis parameters, and their ORR performances are systematically investigated. Although pristine 3D Fe-WO3 NF or reduced graphene oxides show poor catalytic performance and even their hybrid shows unsatisfactory results, impressively, the excellent ORR activity and its outstanding durability are further improved by N doping, especially due to pyridinic and graphitic nitrogen moieties into a graphene sheet. Remarkably, 3D Fe-WO3 NF/NG hybrid nanoarchitecture reveals an outstanding electrocatalytic performance with a remarkable onset potential value (∼0.98 V), a half-wave potential (∼0.85 V) versus relative hydrogen electrode, significant methanol tolerance, and extraordinary durability of ∼95% current retention, even after 15 000 potential cycles, which is superior to a commercial Pt/C. The exclusive porous architecture, excellent electrical conductivity, and the high synergistic interaction between 3D Fe-WO3 NF and NG sheets are the beneficial phenomena for such admirable catalytic performance. Therefore, this finding endows design of a highly efficient and durable nonprecious metal-based electrocatalyst for high-performance ORR in alkaline media.