1,856 results match your criteria: "College of Chemistry and Materials Engineering[Affiliation]"

Improving the fast-charging capability of NbWO-based Li-ion batteries.

Nat Commun

March 2025

College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, China.

The discovery of Nb-W-O materials years ago marks the milestone of charging a lithium-ion battery in minutes. Nevertheless, for many applications, charging lithium-ion battery within one minute is urgently demanded, the bottleneck of which largely lies in the lack of fundamental understanding of Li storage mechanisms in these materials. Herein, by visualizing Li intercalated into representative NbWO, we find that the fast-charging nature of such material originates from an interesting rate-dependent lattice relaxation process associated with the Jahn-Teller effect.

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An Activatable NIR YbZn Cluster for the Detection of Quercetin: Analysis of Host-Guest Interaction and Sensing Mechanism.

Inorg Chem

March 2025

Key Laboratory of Material Chemistry for Energy Conversion and Storage, Semiconductor Chemistry Center, School of Chemistry and Chemical Engineering, Hubei Key Laboratory of Bioinorganic Chemistry & Materia Medica, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.

A rod-like YbZn nanocluster was constructed, which could be an activatable NIR probe for quercetin, with a short response time (5 s) and a low detection limit (0.75 μM). Theoretical simulations reveal that strong π···π interactions and hydrogen bonding result in good orbital overlap for charge transfer from quercetin to the cluster.

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Nanozymes offer diverse therapeutic potentials for cancer treatment which is dependent on the development of nanomaterials. Quasi-metal-organic framework is a class of metal-organic framework-derived nanomaterials with a transition state from metal-organic frameworks towards metal oxide featuring porous structure and high activity. Herein an iron-based quasi-metal-organic framework nanozyme Q-MIL-53(Fe) is reported via a controlled deligandation strategy, exhibiting enhanced peroxidase-/catalase-mimic activity and glutathione depletion capacity, whose underlying mechanisms are studied via density functional theory calculations.

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Deep learning-aided preparation and mechanism revaluation of waste wood lignocellulose-based flame-retardant composites.

Int J Biol Macromol

March 2025

Zhejiang A&F University, College of Chemistry and Materials Engineering, Hangzhou 311300, PR China; Key Laboratory of Wood Science and Technology of Zhejiang Province, Hangzhou 311300, PR China. Electronic address:

Wood and its derivatives play a decisive role in traditional Chinese architecture. Waste wood as a major source of garbage in the construction industry represents a valuable source. The efficient recycling of waste wood has become an urgent technical problem in waste recycling research.

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Crystal Structure Prediction Meets Artificial Intelligence.

J Phys Chem Lett

March 2025

College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China.

Crystal structure prediction (CSP) represents a fundamental research frontier in computational materials science and chemistry, aiming to predict thermodynamically stable periodic structures from given chemical compositions. Traditional methods often face challenges such as high computational costs and local minima trapping. Recently, artificial intelligence methods, represented by generative adversarial networks (GANs), variational autoencoders (VAEs), diffusion models, and large language models (LLMs), have revolutionized the traditional prediction paradigm.

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Rational design of a near-infrared fluorescent probe for rapid monitoring of carboxylesterase in live cells and drug-induced liver injury mice.

Anal Chim Acta

April 2025

College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, 325035, PR China; Key Lab of Biohealth Materials and Chemistry of Wenzhou, Wenzhou University, Wenzhou, 325035, PR China. Electronic address:

Background: Carboxylesterase (CE) is an important enzyme that mainly exists in liver cells and can catalyze the hydrolysis of esters in a variety of pharmaceuticals and xenobiotics. Real-time and non-invasive imaging of CE is of great significance for the study of CE-related metabolic diseases. Although fluorescence sensing technology is considered a promising candidate, the slow response rate (> 60 min), low sensitivity, and short emission wavelength (<650 nm) of most CE probes limit their practical application.

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Polyphenols are closely related to human health, but thermal treatment causes the loss of polyphenol activity. Complexation between amylose and polyphenol prevents oxidation and degradation of polyphenols during thermal treatment. And the functional properties of the complex are affected by the polyphenol backbone.

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Sodium-ion batteries are regarded as one of the most promising alternatives to lithium-ion batteries due to the greater abundance and lower cost of sodium compared to lithium. However, sodium-ion batteries have not yet been widely adopted. The main reason is that, compared to lithium-ion batteries, sodium-ion batteries have lower energy density and shorter cycle life, with the performance of anode materials directly affecting the energy density and cycle stability of sodium-ion batteries.

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Hard, flexible, transparent, and hydrophobic multifunctional coatings have a wide range of applications, but they do not adequately protect against harsh conditions, especially photoaging. In this study, SiO and AlO nanoparticles were first modified by silazane and epoxy-functionalized silanes and then reacted with a polyetheramine curing agent to prepare highly crosslinked multifunctional hybrid coatings at room temperature. Due to the integration of siloxane nanoparticles and a polymer network, the multifunctional coatings presented outstanding hardness (4H), flexibility (bending diameter of 10 mm), and transmittance (>97%).

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In this work, the Cu single-atom catalysts (SACs) supported by metal-oxides (AlO-Cu, CeO-Cu, and TiO-Cu) are used as theoretical models to explore the correlations between electronic structures and CORR performances. For these catalysts, the electronic metal-support interaction (EMSI) induced by charge transfer between Cu sites and supports subtly modulates the Cu electronic structure to form different highest occupied-orbital. The highest occupied 3d orbital of AlO-Cu enhances the adsorption strength of CO and weakens C-O bonds through 3d-π* electron back-donation.

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Atomic Symbiotic-Catalyst for Low-Temperature Zinc-Air Battery.

Angew Chem Int Ed Engl

February 2025

Fachgebiet Angewante Nanophysik, Institut für Physik & IMN MacroNano (ZIK), Technische Universität Ilmenau, Ilmenau, 98693, Germany.

Atomic-level designed electrocatalysts, including single-/dual-atom catalysts, have attracted extensive interests due to their maximized atom utilization efficiency and increased activity. Herein, a new electrocatalyst system termed as "atomic symbiotic-catalyst", that marries the advantages of typical single-/dual-atom catalysts while addressing their respective weaknesses, was proposed. In atomic symbiotic-catalyst, single-atom MN and local carbon defects formed under a specific thermodynamic condition, act synergistically to achieve high electrocatalytic activity and battery efficiency.

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Schiff Base-Crosslinked Tetra-PEG-BSA Hydrogel: Design, Properties, and Multifunctional Functions.

J Funct Biomater

February 2025

College of Food Science and Nutritional Engineering, China Agricultural University, 17 Qinghua Donglu, Haidian District, Beijing 100083, China.

Hydrogel network structures play a crucial role in determining mechanical properties and have broad applications in biomedical and industrial fields. Therefore, their rational design is essential. Herein, we developed a Schiff base-crosslinked hydrogel through the reaction of Tetra-armed polyethylene glycol with aldehyde end groups (Tetra-PEG-CHO) and bovine serum albumin (BSA) under alkaline conditions.

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The inverted cesium/formamidinium (CsFA)-based methylammonium-free perovskite solar cells possess great potential in simultaneously realizing high power conversion efficiency (PCE) and excellent stability. However, the uncontrollable crystallization process and poor film quality hinder further enhancement of photovoltaic performance and operational stability. Herein, we propose a synergistic modulation strategy of perovskite crystallization and the defects at grain boundaries (GBs) and interface by using a novel carbonyl functionalized spacer cation.

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Introduction: The use of polydeoxyribonucleotide (PDRN) in promoting tissue repair and anti-aging has been hindered by several challenges, including its large molecular weight, susceptibility to decomposition, low bioavailability, and poor stability and skin permeability. Liposome formulation technology has emerged as a promising method in cosmetics, enhancing the penetration and protection of active ingredients.

Method: In this study, a PDRN-loaded nanoliposomal (PDRN-NL) formulation, which exhibited an average particle size of 125 ± 1 nm, a polydispersity index (PDI) of 0.

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Poly(vinylidene fluoride) (PVDF)-based solid-state electrolytes (SSEs) have been considered promising candidates for advanced Li metal batteries due to their adequate mechanical strength and acceptable thermal stability. However, the poor compatibility between residual solvent and Li metal inevitably leads to fast capacity decay. Herein, we propose a multifunctional cation-anchor strategy to regulate solvation chemistry in PVDF-based SSEs to boost the electrochemical performance of Li metal batteries.

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Modulating ion-dipole interactions in nonflammable phosphonate-based electrolyte for safe and stable sodium-ion pouch cells.

Natl Sci Rev

March 2025

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China.

Phosphonate-based electrolytes with the merits of low cost and intrinsic nonflammability are promising candidates to realize the safe operation of sodium-ion batteries. However, they generally suffer from poor interfacial chemistry because of the solvent-dominated solvation structure induced by the strong ion-dipole interactions between cations and phosphonate molecules. Herein, we report an electrolyte design strategy that selectively improves the competitive coordination of low-solvating-power molecules, achieving stable interfacial chemistry with a non-flammable, low-cost and fluorine-free electrolyte.

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Activating the high-potential V/V redox couple for an advanced NASICON sodium-ion cathode.

Chem Commun (Camb)

March 2025

Hunan Provincial Key Laboratory of Chemical Power Sources, College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, P. R. China.

NaVCrTi(PO) with multi-electron redox reactions is designed for high-energy-density sodium-ion batteries. The partial Cr substitution achieves high-potential V activation, achieving an ultra-high capacity of 183.07 mA h g at 20 mA g with 89% retention after 1500 cycles at 1 A g.

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Developing high-performance electrodes derived from cellulosic wastes is an effective strategy for promoting large-scale energy storage and achieving carbon neutrality, yet how to enhance capacitive activity from the perspective of surface-interface structure regulation remains a challenge. Herein, a disulfide bond reinforced self-assembly of cellulosic wastes strategy is demostrated to fabricate 3D carbon foams with thiram and bio-straws as examples. The cellulose-enriched piths of straws (EP) are impregnated with thiram solution followed by pyrolysis, where thiram can form a stable 3D cross-linked networks via disulfide-centered hydrogen bonds reinforced self-assembly of EP and thiram, endowing the obtained starfish-like skeleton connected 3D carbon foams with high N/S contents and hierarchical porous structure.

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Poly(lactic acid) (PLA) is a widely reusable polymer, but its practical applications are greatly constrained by low toughness and poor crystallinity. In this study, the modified cellulose nanocrystal (CNC) was designed as a reinforcement through surface copolymerization of caprolactone (CL) and allyl caprolactone (ACL) to enhance the properties of PLA. The surface molecular engineering of reactive core-shell nanofillers (allyl polycaprolactone-grafted CNC, or CNC-g-APCL) effectively improved the interfacial compatibility between PLA and CNC through a straightforward in situ reactive extrusion process.

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NBS-mediated C(sp)-H amidation of -dimethylamides with -acyloxyamides.

Chem Commun (Camb)

March 2025

College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China.

Presented herein is the NBS-mediated amidation of the C(sp)-H bond adjacent to the nitrogen atom of ,-dimethylamide using -acyloxyamide as the amide source, leading to a diverse array of methylenebisamides. The transformation features mild conditions, excellent functional group tolerance, and high efficiency. The practicality of the methodology was shown by gram-scale synthesis and efficient product derivatization.

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Co-MOF-derived carbon nanomaterials with size-controlled FeCo alloys for oxygen evolution.

Chem Commun (Camb)

March 2025

Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, Zhejiang, P. R. China.

A porous carbon material with size-controlled FeCo alloys and carbon nanotubes (CNTs) was obtained from pyrolysis of a Co-based metal-organic framework (MOF), followed by the Fe-etching process and CNT growth. This catalyst (CoOF-1-FeCoNC-CNT) displayed satisfactory OER activity, attributed to its large specific surface area, improved electrical conductivity, and the synergistic effect of the bimetallic FeCo alloy.

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Lignin is an abundant and cost-effective aromatic polymer, which makes the production of high-value aromatic aldehydes from it highly significant. However, a challenge is that these aldehydes can easily over-oxidation into aromatic acids during aerobic oxidation. Therefore, preventing over-oxidation is crucial.

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Li-O batteries urgently needs high discharge capacity and stable cycling performance, requiring effective and reliable bifunctional catalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Herein, Hovenia acerba Lindl-like heterostructure composed of cobalt sulfide and tin dioxide supported on carbon substrate (CoS/SnO@C) is prepared via CO laser irradiation technology. The half-wave potential of CoS/SnO@C for the ORR is 0.

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Synthesis of YFeO-YFeO Heterogeneous Structure Magnetic Nanomaterials and Preparation of Nanofibers by Coprecipitation Method.

Inorg Chem

February 2025

Institute of Advanced Chemical Power Source, College of Chemistry and Materials Engineering, Bohai University, Jinzhou 121013, Liaoning, China.

The design and fabrication of yttrium iron oxide-based magnetic nanomaterials play an indispensable role in microelectronic-related fields. The bottleneck still remains, including limited reproducibility and the inability to control the size of the resulting material. In this study, a straightforward coprecipitation method was firstly used for the production of heterogeneous YFeO-YFeO composite with (NH)CO as the precipitant.

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Recent advances in electrochemical 1,2-difunctionalization of alkenes: mechanisms and perspectives.

Org Biomol Chem

March 2025

Institute of New Materials and Industrial Technologies, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, 325035, P. R. China.

In recent years, significant achievements have been made in the field of electroorganic chemistry regarding the difunctionalization of alkenes. Researchers have developed innovative strategies utilizing the unique reactivity of electrochemical processes to synthesize complex molecules with high regioselectivity and stereoselectivity. This technology is widely applied in the total synthesis of natural products and in the pharmaceutical industry.

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