Synergistic Enhancement of Cathode Performance through the Introduction of Oxygen Vacancies in the P2/P3 Mixed Phase.

P2-type NaNiMnO cathodes have attracted attention due to their excellent stability and low cost, making them promising for sodium-ion batteries. However, their practical application is limited by a low capacity at lower voltages and severe phase transitions at higher voltage. To address these challenges, we report a material NaNiMnO-OVs (NNMO-OVs) with significantly slowed phase transitions at high voltage by introducing oxygen vacancies OVs into the P2/P3 mixed phase cathode NaNiMnO (NNMO).

Regulating Anode-Electrolyte Interphasial Reactions by Zwitterionic Binder Chemistry in Lithium-Ion Batteries with High-Nickel Layered Oxide Cathodes and Silicon-Graphite Anodes.

The practical application of silicon (Si)-based anodes faces challenges due to severe structural and interphasial degradations. These challenges are exacerbated in lithium-ion batteries (LIBs) employing Si-based anodes with high-nickel layered oxide cathodes, as significant transition-metal crossover catalyzes serious parasitic side reactions, leading to faster cell failure. While enhancing the mechanical properties of polymer binders has been acknowledged as an effective means of improving solid-electrolyte interphase (SEI) stability on Si-based anodes, an in-depth understanding of how the binder chemistry influences the SEI is lacking.

Associations of Various Physical Activities with Mortality and Life Expectancy are Mediated by Telomere Length.

Objectives: Physical activity (PA) and telomeres both contribute to healthy aging and longevity. To investigate the optimal dosage of various PA for longevity and the role of telomere length in PA and mortality.

Design: Prospective cohort study.

Composite polymer electrolytes with ionic liquid grafted-Laponite for dendrite-free all-solid-state lithium metal batteries.

Composite polymer electrolytes (CPEs) with high ionic conductivity and favorable electrolyte/electrode interfacial compatibility are promising alternatives to liquid electrolytes. However, severe parasitic reactions in the Li/electrolyte interface and the air-unstable inorganic fillers have hindered their industrial applications. Herein, surface-edge opposite charged Laponite (LAP) multilayer particles with high air stability were grafted with imidazole ionic liquid (IL-TFSI) to enhance the thermal, mechanical, and electrochemical performances of polyethylene oxide (PEO)-based CPEs.

Laponite-Supported Gel Polymer Electrolyte with Multiple Lithium-Ion Transport Channels for Stable Lithium Metal Batteries.

Lithium metal batteries have emerged as a promising candidate for next-generation power systems. However, the high reactivity of lithium metal with liquid electrolytes has resulted in decreased battery safety and stability, which poses a significant challenge. Herein, we present a modified laponite-supported gel polymer electrolyte (LAP@PDOL GPE) that was fabricated using in situ polymerization initiated by a redox-initiating system at ambient temperature.

In situ Interweaved Binder Framework Mitigating the Structural and Interphasial Degradations of High-nickel Cathodes in Lithium-ion Batteries.

The practical viability of high-nickel layered oxide cathodes is compromised by the interphasial and structural degradations. Herein, we demonstrate that by applying an in situ interweaved binder, the cycling stability of high-nickel cathodes can be significantly improved. Specifically, the results show that the resilient binder network immobilizes the transition-metal ions, suppresses electrolyte oxidative decomposition, and mitigates cathode particles pulverization, thus resulting in suppressed cathode-to-anode chemical crossover and ameliorated chemistry and architecture of electrode-electrolyte interphases.

Bifunctional Solid-State Copolymer Electrolyte with Stabilized Interphase for High-Performance Lithium Metal Battery in a Wide Temperature Range.

Solid-state polymer electrolytes (SPEs) are expected to guarantee safe and durable operations of lithium metal batteries (LMBs). Herein, inspired by the salutary poly(vinyl ethylene carbonate) (PVEC) component in the solid electrolyte interphase, cross-linking vinyl ethylene carbonate and ionic liquid copolymers were synthesized by in-situ polymerization to serve as polymer electrolyte for LMBs. On one hand, due to rich ester bonds of PVEC, Li could transfer by coupling/decoupling with oxygen atoms.

Dual Cross-Linked Fluorinated Binder Network for High-Performance Silicon and Silicon Oxide Based Anodes in Lithium-Ion Batteries.

In next generation lithium-ion batteries (LIBs), silicon is a promising electrode material due to its surprisingly high specific capacity, but it suffers from serious volume changes during the lithiation/delithiation process which gradually lead to the destruction of the electrode structure. A novel fluorinated copolymer with three different polar groups was synthesized to overcome this problem: carboxylic acid, amide, and fluorinated groups on a single polymer backbone. Moreover, a dual cross-linked network binder was prepared by thermal polymerization of the fluorinated copolymer and sodium alginate.

Highly Stable Amphiphilic Organogel with Exceptional Anti-icing Performance.

Various organogel materials with either a liquid or solid surface layer have recently been designed and prepared. In this work, amphiphilic organogels (AmOG) are innovatively developed from copolymer P(PDMS-r-PEG-r-GMA) and 2,2'-diaminodiphenyldisulfide via epoxy group addition reaction and then infiltrated with amphiphilic lubricants instead of traditional hydrophilic or hydrophobic lubricants. Because of synergistic effects of hydrophilic and hydrophobic segments of amphiphilic lubricants, the AmOG surfaces showed high stability and excellent anti-icing performance.

Silicone Oil Swelling Slippery Surfaces Based on Mussel-Inspired Magnetic Nanoparticles with Multiple Self-Healing Mechanisms.

In this work, a novel substrate building block, magnetic FeO nanoparticles armed with dopamine molecules were developed via mussel-inspired metal-coordination bonds. Combined with glycidyl methacrylate, polydimethylsiloxane propyl ether methacrylate, and diethylenetriamine, the original silicone oil swelling slippery liquid-infused porous surfaces (SLIPS) were first prepared by reversible coordinate bonds and strong covalent bonds cross-linking process. The matrix mechanical characteristics and surface physicochemical properties were systematically investigated.

pH-Induced Switchable Superwettability of Efficient Antibacterial Fabrics for Durable Selective Oil/Water Separation.

The superhydrophobic antibacterial fabrics with intelligent switchable wettability were fabricated by the cross-link reaction among pH-responsive antibacterial copolymer tethered hydroxyl groups, methylol-contained poly(ureaformaldehyde) nanoparticles (PUF NPs), and hexamethylene diisocyanate. It was found that the surface concentration of N were heavily influenced by acid solutions, resulting in the rapid wettability conversion from superhydrophobicity/superoleophilicity to superhydrophilicity/underwater superoleophobicity in a remarkably short time. The above responsiveness feature of coated cotton fabric contributes a prominent selective oil/water separation property, and the separation efficiency invariably remained at greater than 95% even after 20 reuse cycles, which exhibited brilliant durability.

China and the United States--Global partners, competitors and collaborators in nanotechnology development.

USA and China are two leading countries engaged in nanotechnology research and development. They compete with each other for fruits in this innovative area in a parallel and compatible manner. Understanding the status and developmental prospects of nanotechnology in USA and China is important for policy-makers to decide nanotechnology priorities and funding, and to explore new ways for global cooperation on key issues.

Dendrimeric anticancer prodrugs for targeted delivery of ursolic acid to folate receptor-expressing cancer cells: synthesis and biological evaluation.

The anticancer efficacy of ursolic acid (UA) was limited by poor water solubility, non-specific tumor distribution, and low bioavailability. To overcome this problem, polyamidoamine (PAMAM) conjugated with UA and folic acid (FA) as novel dendrimeric prodrugs were designed and successfully synthesized by a concise one-pot synthetic approach. Both FA and UA were covalently conjugated to the surface of PAMAM through acid-labile ester bonds and the covalently linked UA could be hydrolysed either in acidic (pH 5.