Publications by authors named "Lingfei Zhao"

Sepsis-induced acute kidney injury (SI-AKI) is a severe condition with limited therapeutic options, resulting in poor prognosis. Ferroptosis exacerbates the damage caused by SI-AKI, but the mechanisms regulating ferroptosis, especially those involving ubiquitination regulators, remain poorly understood. Here, we used a lipopolysaccharide (LPS)-induced human kidney organoid (HKO) model to investigate ferroptosis in SI-AKI.

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The unstable electrolyte-electrode interface and the trace HO in commercial organic electrolytes critically limit the cycling life of batteries. Herein, a locking-chain sodium 4,4'-(1,4-phenylenebis(oxy))-bis(butane-1-sulfonate)-15-crown-5 (15PBS) is designed for phase-to-interface electrolyte optimization. In the electrolyte phase, the strong hydrophilic sulfonate groups and 15-crown-5 in 15PBS effectively transform HO from a reactive aggregated state (strong H-bond) into an inactive state (weak H-bond) through adsorption, effectively suppressing HO-induced electrolyte decomposition.

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In contrast to high-concentration electrolyte systems, low-concentration electrolytes provide a cost-effective strategy to advance the commercialization of aqueous zinc-ion batteries (AZIBs). However, such electrolytes frequently exhibit severe dendrite formation caused by localized Zn concentration gradients, which critically compromise the cycling stability and operational safety of AZIBs. In this work, an innovative approach is proposed that involves the in situ construction of a fluoride-ion (F) enriched interfacial layer on zinc anodes.

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Aprotic Li-CO batteries (LCBs) hold promise for mitigating the greenhouse effect while generating electric power, yet their development remains nascent due to the sluggish CO activation and irreversible discharge product formation, requiring efficient catalysts to address these challenges. Herein, we developed ∼5.5 nm fcc + hcp Ru heterophase nanoparticles on a Ketjen black (KB) matrix (Ru/KB) as a dual-functional catalyst for LCBs.

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Resource-friendly photorechargeable sodium batteries (PRSBs) integrate energy storage devices with solar cells, offering a promising path for sustainable energy. Herein, a novel TiO/CdSe/NaFe(PO)PO (NFPP) cathode was prepared layer-by-layer utilizing resource-abundant commercialized NFPP and photoactive CdSe. The aligned energy levels with type II band structure ensure effective transfer of photogenerated holes from CdSe (-5.

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The profound understanding of chemical reaction essence and kinetic behaviors is crucial to develop rechargeable battery technologies. Based on multi-electron conversion, sulfur redox reactions hold great promise for establishing low-cost, high-energy-density, and longstanding rechargeable batteries. However, the sulfur redox reaction processes suffer from a series of common daunting cruxes, leading to incomplete redox reactions and inferior battery performance when working in rechargeable batteries.

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Multiterminal Josephson circuits have been proposed as a promising platform to host synthetic topological phases of matter, Floquet states, and multiplet supercurrents that are mediated by pairs of Cooper pairs. Here, we explore a Josephson circuit in which three superconducting electrodes are connected through Josephson junctions to a common superconducting island. We demonstrate the dynamic generation of the multiplet supercurrents, which are found to be robust to elevated temperatures and are confirmed by exhibiting the expected Shapiro step quantization under a microwave drive.

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An important route of engineering topological states and excitations is to combine superconductors (SC) with the quantum Hall (QH) effect, and over the past decade, significant progress has been made in this direction. While typical measurements of these states focus on electronic properties, little attention has been paid to the accompanying thermal responses. Here, we examine the thermal properties of the interface between type-II superconducting electrodes and graphene in the QH regime.

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Polymer electrolytes incorporated with fillers possess immense potential for constructing the fast and selective Li conduction. However, the inhomogeneous distribution of the fillers usually deteriorates the microdomain consistency of the electrolytes, resulting in uneven Li flux, and unstable electrode-electrolyte interfaces. Herein, we formulate a solution-process chemistry to in situ construct gel polymer electrolytes (GPEs) with well-dispersed metal-organic frameworks (MOFs), leading to a uniform microdomain structure.

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Biomass holds significant potential for large-scale synthesis of hard carbon (HC), and HC is seen as the most promising anode material for sodium-ion batteries (SIBs). However, designing a HC anode with a rich pore structure, moderate graphitization and synthesis through a simple process using a cost-effective precursor to advance SIBs has long been a formidable challenge. This is primarily because high temperatures necessary for pore regulation invariably lead to excessive graphitization.

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Anode-free sodium metal batteries represent great promising as high-energy-density and resource-rich electrochemical energy storage systems. However, the savage growth of sodium metal and continuous consumption hinder its stable capacity output. Herein, ordered flower-edges of zinc on Al substrate can induce high-entropy solid electrolyte interphase (SEI) to adjust sodium uniform deposition and extremely reduce electrolyte consumption with ultrahigh initial Coulombic efficiency (97.

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The establishment of a tolerant space to realize the co-stimulation of cytokines and contact-dependent molecules remain challenging in allotransplant. Here, an injectable genetically engineered hydrogel (iGE-Gel) is reported, which developed with a multivalent network of FOXP3 engineered extracellular vesicles (Foe-EVs) through the hydrophobic interaction between stearic acid modified hyaluronic acid (HASA) and the membrane phospholipids of extracellular vesicles (EVs). The iGE-Gel exhibited self-healing properties, injectability and biocompatibility.

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The environmental problems caused by the abuse of antibiotics are raising serious attention, and the removal of antibiotics in wastewater is meaningful yet challenging. In this work, lignin-derived carbon fibers loaded layered double hydroxides (LDH@LCF) has been prepared for the removal of ofloxacin (OFX) from wastewater via photocatalysis, which exhibit a high degradation efficiency of 96 % under visible light and maintained 90 % after five reuses. The effects of Zn/Fe in the samples and other parameters affecting the photocatalytic efficiency of OFX have been systematically investigated.

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Rechargeable batteries have been indispensable for various portable devices, electric vehicles, and energy storage stations. The operation of rechargeable batteries at low temperatures has been challenging due to increasing electrolyte viscosity and rising electrode resistance, which lead to sluggish ion transfer and large voltage hysteresis. Advanced electrolyte design and feasible electrode engineering to achieve desirable performance at low temperatures are crucial for the practical application of rechargeable batteries.

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The need for efficient, economical, and clean energy systems is increasing, and as a result, interest in water-splitting techniques to produce green hydrogen is also increasing. However, the sluggish kinetics of the oxygen evolution reaction (OER) hinders the practical application and widespread use of water-splitting technologies; therefore, to address this challenge, it is essential to develop cost-effective and efficient OER catalysts. In this work, we have synthesized an inexpensive and tunable FeCoMn Prussian blue analogue (PBAs) as an efficient OER catalyst via a straightforward process.

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The osteoporotic bone defect caused by excessive activity of osteoclasts has posed a challenge for public healthcare. However, most existing bioinert bone cement fails to effectively regulate the pathological bone microenvironment and reconstruct bone homeostasis in the presence of osteoclast overactivity and osteoblast suppression. Herein, inspired by natural bone tissue, an in-situ modulation system for osteoporotic bone regeneration is developed by fabricating an injectable double-crosslinked PEGylated poly(glycerol sebacate) (PEGS)/calcium phosphate cement (CPC) loaded with sodium alendronate (ALN) (PEGS/CPC@ALN) adhesive bone cement.

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Article Synopsis
  • This study evaluated the knowledge, attitudes, and practices (KAP) of patients with diabetes and hyperuricemia regarding their self-management of these conditions.
  • Conducted at Heilongjiang Provincial Hospital, the research included a web-based questionnaire distributed to 482 participants, revealing insights into their demographics and KAP scores.
  • The findings show that while patients had relatively good KAP scores, there was room for improvement, suggesting that enhancing understanding and attitudes toward their health could lead to better self-management outcomes.
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Fracture represents one of the most common diagnoses in contemporary medical practice, with the majority of cases traditionally addressed through metallic device fixation. However, this approach is marred by several drawbacks, including prolonged operative durations, considerable expenses, suboptimal applicability to comminuted fractures, increased infection risks, and the inevitable requirement for secondary surgery. The inherent advantages of bone adhesives in these fields have garnered the attention of orthopedic surgeons, who have commenced utilizing biocompatible and biodegradable bone adhesives to bond and stabilize bone fragments.

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  • Proton-coupled electron transfer (PCET) reactions at electrified interfaces are crucial for the oxygen reduction reaction (ORR), and this study focuses on enhancing these reactions using a specific catalyst.
  • The researchers developed a FeC water activation site in carbon nanofibers (Fe-N co-doped carbon nanofibers) through a combination of electrospinning, pyrolysis, and etching techniques, which improves hydrogen bonding with oxygen intermediates.
  • Their findings indicate that delocalized electrons from the Fe-N sites facilitate the dissociation of interfacial water, enhancing ORR kinetics, with the FeC-Fe/CNT catalyst achieving impressive half-wave potentials of
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Lithium (Li) metal is one of the most promising anode materials for next-generation, high-energy, Li-based batteries due to its exceptionally high specific capacity and low reduction potential. Nonetheless, intrinsic challenges such as detrimental interfacial reactions, significant volume expansion, and dendritic growth present considerable obstacles to its practical application. This review comprehensively summarizes various recent strategies for the modification and protection of metallic lithium anodes, offering insight into the latest advancements in electrode enhancement, electrolyte innovation, and interfacial design, as well as theoretical simulations related to the above.

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The development of cost-efficient, long-lifespan, and all-climate sodium-ion batteries is of great importance for advancing large-scale energy storage but is plagued by the lack of suitable cathode materials. Here, we report low-cost Na-rich Mn-based Prussian blue analogues with superior rate capability and ultralong cycling stability over 10,000 cycles via structural optimization with electrochemically inert Ni atoms. Their thermal stability, all-climate properties, and potential in full cells are investigated in detail.

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Article Synopsis
  • Achieving both high-energy-density and high-power-density in power batteries is challenging, but this study uses atomic layer deposition (ALD) and thermal treatments to create an innovative protective coating on commercial LiNiCoMnO (NCM523) cathodes.
  • The new coating, which features dual conduction, prevents unwanted reactions and promotes lithium transport, enhancing stability and performance at high voltages.
  • The modified battery, Al@EIC-NCM523, shows impressive results with a capacity of 114.7 mAh/g at high rates and retains 74.72% of its capacity after 800 charge cycles, indicating potential for future lithium-ion battery advancements.
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  • The development of high-voltage Lithium Cobalt Oxide (LiCoO or LCO) materials is crucial for improving energy densities in smart electronics, but faces challenges, including interface degradation and structural collapse at 4.7 V.
  • A novel approach combining an ultra-thin LiAlO coating and gradient aluminum doping addresses these issues by enhancing Li migration and electrochemical stability while reducing side reactions.
  • The modified LCO shows significant improvements, achieving a reversible capacity of 230 mAh/g at 4.7 V and excellent cycling stability, making it a promising candidate for high-energy-density electrode materials.
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  • Scientists are studying P3-layered transition oxide cathodes because they can hold a lot of energy and work quickly for sodium-ion batteries.
  • However, they have a problem where their performance decreases over time due to changes in their structure and the movement of manganese particles.
  • To fix this, researchers created a special material that combines P3 with another structure (spinel), which helps the batteries last longer and perform better.
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The effective flow of electrons through bulk electrodes is crucial for achieving high-performance batteries, although the poor conductivity of homocyclic sulfur molecules results in high barriers against the passage of electrons through electrode structures. This phenomenon causes incomplete reactions and the formation of metastable products. To enhance the performance of the electrode, it is important to place substitutable electrification units to accelerate the cleavage of sulfur molecules and increase the selectivity of stable products during charging and discharging.

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