Ternary Mo2 NiB2 as a Superior Bifunctional Electrocatalyst for Overall Water Splitting.

Transition metal borides are considered as promising electrocatalysts for water splitting due to their metallic conductivity and good durability. However, the currently reported monometallic and noncrystalline multimetallic borides only show generic and monofunctional catalytic activity. In this work, the authors design and successfully synthesize highly crystalline ternary borides, Mo2 NiB2 , via a facile solid-state reaction from pure elemental powders. The as-synthesized Mo2 NiB2 exhibits very low overpotentials for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), that is, 280 and 160 mV to reach a current density of 10 mA cm-2 , in alkaline media. These values are much lower from the ones observed over monometallic borides, that is, Ni2 B and MoB, and the lowest among all nonprecious metal borides. By loading Mo2 NiB2 onto Ni foams as both cathode and anode electrode for overall water splitting applications, a low cell voltage of 1.57 V is required to achieve a current density of 10 mA cm-2 , comparable with the value required from the Pt/C||IrO2 /C couple (1.56 V). The proposed synthesis strategy can be used for the preparation of cost-effective, multi-metallic crystalline borides, as multifunctional electrocatalysts.

3D Nitrogen-Doped Graphene Encapsulated Metallic Nickel-Iron Alloy Nanoparticles for Efficient Bifunctional Oxygen Electrocatalysis.

Invited for the cover of this issue is Liqiang Mai and co-workers at Wuhan University of Technology. The image depicts Ni3 Fe alloy nanoparticles encapsulated in N-doped graphene as an efficient bifunctional oxygen electrocatalyst toward rechargeable Zn-air batteries, which is expected to drive the electric vehicle. Read the full text of the article at 10.1002/chem.201904722.

3D Nitrogen-Doped Graphene Encapsulated Metallic Nickel-Iron Alloy Nanoparticles for Efficient Bifunctional Oxygen Electrocatalysis.

It is extremely desirable to explore high-efficient, affordable and robust oxygen electrocatalysts toward rechargeable Zn-air batteries (ZABs). A 3D porous nitrogen-doped graphene encapsulated metallic Ni3 Fe alloy nanoparticles aerogel (Ni3 Fe-GA1 ) was constructed through a facile hydrothermal assembly and calcination process. Benefiting from 3D porous configuration with great accessibility, high electrical conductivity, abundant active sites, optimal nitrogen content and strong electronic interactions at the Ni3 Fe/N-doped graphene heterointerface, the obtained aerogel showed outstanding catalytic performance toward the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Specifically, it exhibited an overpotential of 239 mV to attain 10 mA cm-2 for OER, simultaneously providing a positive onset potential of 0.93 V within a half-wave potential of 0.8 V for ORR. Accordingly, when employed in the aqueous ZABs, Ni3 Fe-GA1 achieved higher power density and superior reversibility than Pt/C-IrO2 catalyst, making it a potential candidate for rechargeable ZABs.

1D Carbon-Based Nanocomposites for Electrochemical Energy Storage.

Electrochemical energy storage (EES) devices have attracted immense research interests as an effective technology for utilizing renewable energy. 1D carbon-based nanostructures are recognized as highly promising materials for EES application, combining the advantages of functional 1D nanostructures and carbon nanomaterials. Here, the recent advances of 1D carbon-based nanomaterials for electrochemical storage devices are considered. First, the different categories of 1D carbon-based nanocomposites, namely, 1D carbon-embedded, carbon-coated, carbon-encapsulated, and carbon-supported nanostructures, and the different synthesis methods are described. Next, the practical applications and optimization effects in electrochemical energy storage devices including Li-ion batteries, Na-ion batteries, Li-S batteries, and supercapacitors are presented. After that, the advanced in situ detection techniques that can be used to investigate the fundamental mechanisms and predict optimization of 1D carbon-based nanocomposites are discussed. Finally, an outlook for the development trend of 1D carbon-based nanocomposites for EES is provided.

Binder-Free Anodes for Potassium-ion Batteries Comprising Antimony Nanoparticles on Carbon Nanotubes Obtained Using Electrophoretic Deposition.

Antimony has a high theoretical capacity and suitable alloying/dealloying potentials to make it a future anode for potassium-ion batteries (PIBs); however, substantial volumetric changes, severe pulverization, and active mass delamination from the Cu foil during potassiation/depotassiation need to be overcome. Herein, we present the use of electrophoretic deposition (EPD) to fabricate binder-free electrodes consisting of Sb nanoparticles (NPs) embedded in interconnected multiwalled carbon nanotubes (MWCNTs). The anode architecture allows volume changes to be accommodated and prevents Sb delamination within the binder-free electrodes. The Sb mass ratio of the Sb/CNT nanocomposites was varied, with the optimized Sb/CNT nanocomposite delivering a high reversible capacity of 341.30 mA h g-1 (∼90% of the initial charge capacity) after 300 cycles at C/5 and 185.69 mA h g-1 after 300 cycles at 1C. Postcycling investigations reveal that the stable performance is due to the unique Sb/CNT nanocomposite structure, which can be retained over extended cycling, protecting Sb NPs from volume changes and retaining the integrity of the electrode. Our findings not only suggest a facile fabrication method for high-performance alloy-based anodes in PIBs but also encourage the development of alloying-based anodes for next-generation PIBs.

3D mesoporous structure assembled from monoclinic M-phase VO2 nanoflakes with enhanced thermochromic performance.

Monoclinic M-phase VO2 is a promising candidate for thermochromic materials due to its abrupt change in the near infrared (NIR) transmittance along with the metal-to-insulator transition (MIT) at a critical temperature ∼68 °C. However, low luminous transmittance (T lum), poor solar energy modulation ability (ΔT sol), and high phase transition temperature (T c) can limit the application of VO2 for smart windows. To overcome these limitations, 3D mesoporous structure can be employed in VO2 films. Herein, 3D mesoporous structures assembled from monoclinic M-phase VO2 nanoflakes with a pore size of about 2-10 nm were synthesized by a hydrothermal method using Ensete ventricosum fiber (EF) as a template followed by calcination at 450 °C. The prepared film exhibited excellent thermochromic performance with balanced T lum = 67.3%, ΔT sol = 12.5%, and lowering T c to 63.15 °C. This is because the 3D mesoporous structure can offer the uniform dispersion of VO2 nanoflakes in the film to enhance T lum, ensure sufficient VO2 nanoflakes in the film for high ΔT sol and lower T c. Therefore, this work can provide a green approach to synthesize 3D mesoporous structures assembled from monoclinic M-phase VO2 nanoflakes and promote their application in smart windows.

Ambient temperature sulfonated carbon fiber reinforced PEEK with hydroxyapatite and reduced graphene oxide hydroxyapatite composite coating.

30% carbon fiber reinforced polyetheretherketone (CFR-PEEK) has in recent times, become significant in the orthopedic industry because its elastic modulus can be engineered to match that of the human bone. But it is bioinert and does not integrate well with the immediate bone tissue environment. In this study, a combined surface modification technique involving ambient temperature sulfonation and surface coating of (hydroxyapatite (HA), 5%reduced graphene oxide hydroxyapatite(5%RGO/HA) and 10%reduced graphene oxide hydroxyapatite(10%RGO/HA) composites) on 30%CFR-PEEK was achieved with an appropriate temperature treatment at 345°C in nitrogen. The coatings adhered unto the surface of S30%CFR-PEEK with an improved hydrophilicity and bioactivity. With the sample S30%CFR-PEEK+HA, having the highest enhanced hydrophilicity from 112.5 ± 2.5° to 20 ± 2° and bioactivity. An improvement in hydrophilicity and bioactivity depicts a change in surface chemistry which will have a positive impact in the interaction of the materials surface with immediate bone environment for a successful application in the orthopedic industry.

Bilayered microelectrodes based on electrochemically deposited MnO2/polypyrrole towards fast charge transport kinetics for micro-supercapacitors.

Micro-supercapacitors (MSCs) are promising power solution facilities for miniaturized portable electronic devices. Microfabrication of on-chip MSC with high specific capacitance and high energy density is still a great challenge. Herein, we report a high-performance MnO2/polypyrrole (PPy) microelectrode based MSC (MnO2/PPy-MSC) by modern micromachining technology. Interdigital Au micro current collectors were obtained by photolithography, physical vapor deposition and lift off. A layer of PPy was electrochemically deposited on Au current collectors followed by deposition of urchin-like MnO2 micro/nanostructures. The electrochemical performance of MnO2/PPy-MSC was explored employing LiClO4/PVA gel electrolyte. The assembled MSC demonstrated a high areal capacitance of 13 mF cm-2, an energy density of 1.07 × 10-3 mW h cm-2 and a power density of 0.53 mW cm-2. In addition, the MnO2/PPy-MSC showed an improved cycling stability, retaining 84% of the initial capacitance after 5000 CV cycles at a scan rate of 500 mV s-1. Our proposed strategy provides a versatile and promising method for the fabrication of high-performance MSCs with large-scale applications.

Macroscopic synthesis of ultrafine N-doped carbon nanofibers for superior capacitive energy storage.

Carbon nanofibers (CNFs) with excellent electric conductivity and high surface area have attracted immense research interests in supercapacitors. However, the macroscopic production of CNFs still remains a great challenge. Herein, ultrafine N-doped CNFs (N-CNFs) with a diameter of ∼20 nm are synthesized through a simple and scalable sol-gel method based on the self-assembly of phenolic resin and cetyltrimethylammonium bromide. When employed in aqueous supercapacitors, the obtained activated N-CNFs manifest a high gravimetric/areal capacitance (380 F g-1/1.7 F cm-2) as well as outstanding rate capability and cycling stability. Besides, the activated N-CNFs also demonstrate excellent capacitive performance (330 F g-1) in flexible quasi-solid-state supercapacitors. The remarkable electrochemical performance as well as the easy and scalable synthesis makes the N-CNFs a highly promising electrode material for supercapacitors.

Boosting oxygen reduction activity with low-temperature derived high-loading atomic cobalt on nitrogen-doped graphene for efficient Zn-air batteries.

High-loading atomic cobalt (12.8 wt%) dispersed on nitrogen-doped graphene was successfully synthesized via considerably low temperature pyrolysis. The catalyst exhibits excellent electrocatalytic performance towards the oxygen reduction reaction with a large limiting diffusion current density of 5.60 mA cm-2 (10% higher than that of commercial Pt/C), and when acting as the air catalyst of Zn-air batteries, a high open-circuit voltage of >1.40 V and excellent power density are also achieved.

Stepwise chelation-etching synthesis of carbon-confined ultrafine SnO2 nanoparticles for stable sodium storage.

A stepwise chelation-etching approach to synthesize carbon-confined ultrafine SnO2 nanoparticles was developed via conformal coating with polydopamine and chelation-etching with ethylenediaminetetraacetic acid (EDTA). EDTA plays a crucial role in the ordered removal of cobalt and tin. The obtained composite exhibits superior sodium storage performance.

Low-crystalline iron oxide hydroxide nanoparticle anode for high-performance supercapacitors.

Carbon materials are generally preferred as anodes in supercapacitors; however, their low capacitance limits the attained energy density of supercapacitor devices with aqueous electrolytes. Here, we report a low-crystalline iron oxide hydroxide nanoparticle anode with comprehensive electrochemical performance at a wide potential window. The iron oxide hydroxide nanoparticles present capacitances of 1,066 and 716 F g-1 at mass loadings of 1.6 and 9.1 mg cm-2, respectively, a rate capability with 74.6% of capacitance retention at 30 A g-1, and cycling stability retaining 91% of capacitance after 10,000 cycles. The performance is attributed to a dominant capacitive charge-storage mechanism. An aqueous hybrid supercapacitor based on the iron oxide hydroxide anode shows stability during float voltage test for 450 h and an energy density of 104 Wh kg-1 at a power density of 1.27 kW kg-1. A packaged device delivers gravimetric and volumetric energy densities of 33.14 Wh kg-1 and 17.24 Wh l-1, respectively.

Porous Nickel-Iron Selenide Nanosheets as Highly Efficient Electrocatalysts for Oxygen Evolution Reaction.

Exploring non-noble and high-efficiency electrocatalysts is critical to large-scale industrial applications of electrochemical water splitting. Currently, nickel-based selenide materials are promising candidates for oxygen evolution reaction due to their low cost and excellent performance. In this work, we report the porous nickel-iron bimetallic selenide nanosheets ((Ni0.75Fe0.25)Se2) on carbon fiber cloth (CFC) by selenization of the ultrathin NiFe-based nanosheet precursor. The as-prepared three-dimensional oxygen evolution electrode exhibits a small overpotential of 255 mV at 35 mA cm(-2) and a low Tafel slope of 47.2 mV dec(-1) and keeps high stability during a 28 h measurement in alkaline solution. The outstanding catalytic performance and strong durability, in comparison to the advanced non-noble metal catalysts, are derived from the porous nanostructure fabrication, Fe incorporation, and selenization, which result in fast charge transportation and large electrochemically active surface area and enhance the release of oxygen bubbles from the electrode surface.