Electron-injection-engineering induced dual-phase MoOF/MoOF heterostructure for magnesium storage.

Rechargeable magnesium batteries (RMBs) have received increased attention due to their high volumetric capacity and safety. Nevertheless, the sluggish diffusion kinetics of highly polarized Mg in host lattices severely hinders the development of RMBs. Herein, we report an electron injection strategy for modulating the Mo 4d-orbital splitting manner and first fabricate a dual-phase MoOF/MoOF heterostructure to accelerate Mg diffusion.

Engineering d-p Orbital Hybridization with P, S Co-Coordination Asymmetric Configuration of Single Atoms Toward High-Rate and Long-Cycling Lithium-Sulfur Battery.

Single-atom catalysts (SACs) have been increasingly explored in lithium-sulfur (Li-S) batteries to address the issues of severe polysulfide shuttle effects and sluggish redox kinetics. However, the structure-activity relationship between single-atom coordination structures and the performance of Li-S batteries remain unclear. In this study, a P, S co-coordination asymmetric configuration of single atoms is designed to enhance the catalytic activity of Co central atoms and promote d-p orbital hybridization between Co and S atoms, thereby limiting polysulfides and accelerating the bidirectional redox process of sulfur.

Ultra-High Proportion of Grain Boundaries in Zinc Metal Anode Spontaneously Inhibiting Dendrites Growth.

Aqueous Zn-ion batteries are an attractive electrochemical energy storage solution for their budget and safe properties. However, dendrites and uncontrolled side reactions in anodes detract the cycle life and energy density of the batteries. Grain boundaries in metals are generally considered as the source of the above problems but we present a diverse result.

Lightweight ZnO/Carbonated Cotton Fiber Nanocomposites for Electromagnetic Interference Applications: Preparation and Properties.

Electromagnetic wave pollution has become a significant harm posed to human health and precision instruments. To shelter such instruments from electromagnetic radiation, high-frequency electromagnetic interference (EMI) shielding materials are extremely desirable. The focus of this research is lightweight, high-absorption EMI shielding composites.

Fabrication of bio-based biodegradable poly(lactic acid) (PLA) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) composite foams for highly efficient oil-water separation.

The open-cell bio-based biodegradable polymer foams show good application prospect in dealing with the serious environmental issue caused by oil spill and organic solvents spills, while the cell structures and hydrophobic properties of the foams limit their performance. In this work, the poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) was selected to help prepare bio-based biodegradable poly(lactic acid) (PLA) foams. Based on a two-step foaming method, the crystallization ability of different samples was regulated by the "original crystals" together with PHBV in the foaming process, where skeleton structures were provided to facilitate the open-cell structures and promote their mechanical property.

Fabrication of poly(lactic acid) foam with high expansion ratio and oriented cellular structure by restricting cold crystallization.

The foaming behavior of semi-crystalline polymers is significantly affected by their crystallization. To achieve high expansion ratio of poly(lactic acid) (PLA) foams, we thought its cold crystallization should be restricted. Therefore, we used a short soaking time of CO to fabricate high-expansion PLA foams.

Tuning Active Metal Atomic Spacing by Filling of Light Atoms and Resulting Reversed Hydrogen Adsorption-Distance Relationship for Efficient Catalysis.

Precisely tuning the spacing of the active centers on the atomic scale is of great significance to improve the catalytic activity and deepen the understanding of the catalytic mechanism, but still remains a challenge. Here, we develop a strategy to dilute catalytically active metal interatomic spacing (d) with light atoms and discover the unusual adsorption patterns. For example, by elevating the content of boron as interstitial atoms, the atomic spacing of osmium (d) gradually increases from 2.

Constrained C adsorbate orientation enables CO-to-acetate electroreduction.

The carbon dioxide and carbon monoxide electroreduction reactions, when powered using low-carbon electricity, offer pathways to the decarbonization of chemical manufacture. Copper (Cu) is relied on today for carbon-carbon coupling, in which it produces mixtures of more than ten C chemicals: a long-standing challenge lies in achieving selectivity to a single principal C product. Acetate is one such C compound on the path to the large but fossil-derived acetic acid market.

Mg Ion Pre-Insertion Boosting Reaction Kinetics and Structural Stability of Ammonium Vanadates for High-Performance Aqueous Zinc-Ion Batteries.

Aqueous zinc-ion batteries (AZIBs) attract much attention owing to their high safety, environmentally friendliness and low cost. However, the unsatisfactory performance of cathode materials is one of the unsolved important factors for their widespread application. Herein, we report NH V O nanorods with Mg ion preinsertion (Mg-NHVO) as a high-performance cathode material for AZIBs.

Lightweight electromagnetic interference shielding poly(L-lactic acid)/poly(D-lactic acid)/carbon nanotubes composite foams prepared by supercritical CO foaming.

Lightweight and biodegradable polymer composites with efficient electromagnetic interference (EMI) shielding performance are of great significance for controlling pollution caused by plastic waste and electromagnetic radiation. Herein, poly(lactic acid) (PLA)/carbon nanotubes (CNTs) composites were prepared through a melt blending method. By adding a small amount of poly(D-lactic acid) to poly(L-lactic acid) (PLLA), the EMI shielding performance of the composites was improved because an enhanced viscoelasticity and suitable crystallinity could help to construct fine CNT conductive networks.

Mechanism of Heterogeneous Bubble Nucleation in Polymer Blend Foaming.

A three-dimensional heterogeneous bubble nucleation model is constructed to provide a reasonable explanation at the molecular level for the foaming mechanism of polypropylene (PP) and polystyrene (PS) blends. CO solubilities and supersaturation rations are quantitatively calculated to help interpret the contribution of each phase of the blend in the CO dissolution stage. The spatial density profiles of polymer/CO binary melt around different polymer chains are presented to give an intuitive perspective to the thermodynamic driving force.