Surfaces and Interfaces
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2024
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IF 5.7
Xiongwei Dong,Qi Sun,Xincan Shi,Zixiong Yin,Beini Zeng,Zheng Huang,Xiang Li
Lyocell fibers, the most successful regenerated cellulose fibers, have already attracted much attention. However, the use of traditional Lyocell fibers in the field of personal protective equipment (PPE) is limited, due to the lack of antibacterial properties. Additionally, the flame-retardant properties of Lyocell fibers are also required for the specific applications. Here, we co-conjugated phosphorus flame retardants and copper-thiosemicarbazone complexes with antibacterial performance on Lyocell fibers through chemical crosslinkers. The chemical composition and morphology of our engineered Lyocell fibers were fully characterized, and their mechanical properties were also maintained. Flame retardants can import flame-retardant properties (LOI: 25.0 % - 25.7 %) to Lyocell fibers, which also show promising antibacterial activity , suppressing Escherichia coli (GIR: 20.51 % - 66.67 %) and Staphylococcus aureus (GIR: 74.19 % - 93.54 %). Such an improved sustainable formulation can be used to produce the next-generation of Lyocell-based PPE, to meet the demand for the antibacterial and flame-retardant properties of fibers in special applications.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2024
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IF 5.8
Jia Li,Wentao Liu,Yang Li,Zhi Liu,Yang Liu
A series of hierarchical flower-like CdS/carbon quantum dots/NiAl-LDH (CCL) photocatalyst have been successfully prepared to achieve efficient conversion of CO 2 -to-CO via a simple yet effective hydrothermal method. In the CCL, interspersed-CQDs not only increase the number of reactive sites but also reduce inner electronic impedance with the assistance of light reflecting-scattering effect. This significantly improves electron migration efficiency and inhibits the recombination of photoinduced electron-holes pairs. Without any sacrificial agent or photosensitizer, the sample of CCL-1 exhibits the highest CO evolution rate of 7.04 μmol·g −1 ·h −1 in water under simulated sunlight illumination with a large specific surface area (129.15 m 2 g −1 ) and an appropriate CQDs content of 15.2 wt%, which is 12.8- and 11.2-fold higher than those of pristine LDH, pure CdS, and many previously reported LDH-based counterparts. A type-Ⅱ interfacial charge transfer mechanism is proposed, where electrons migrate rapidly from CdS to LDH with highly-interspersed CQDs as unhindered electron conduction bridges. The present work outlines a simple and controllable LDH-based heterojunction, which give rise to superior photocatalytic activity for CO 2 photoreduction.
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ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Leikai Zhao,Rui Zhang,Guixin Yang,Yuhang Wang,Shili Gai,Xin Zhao,Mengmeng Huang,Piaoping Yang
Foreseen as foundational in forthcoming oncology interventions are multimodal therapeutic systems. Nevertheless, the tumor microenvironment (TME), marked by heightened glucose levels, hypoxia, and scant concentrations of endogenous hydrogen peroxide could potentially impair their effectiveness. In this research, two-dimensional (2D) Ti3C2 MXene nanosheets are engineered with CeO2 nanozymes and glucose oxidase (GOD), optimizing them for TME, specifically targeting cancer therapy. Following our therapeutic design, CeO2 nanozymes, embodying both peroxidase-like and catalase-like characteristics, enable transformation of H2O2 into hydroxyl radicals for catalytic therapy while also producing oxygen to mitigate hypoxia. Concurrently, GOD metabolizes glucose, thereby augmenting H2O2 levels and disrupting the intracellular energy supply. When subjected to a near-infrared laser, 2D Ti3C2 MXene accomplishes photothermal therapy (PTT) and photodynamic therapy (PDT), additionally amplifying cascade catalytic treatment via thermal enhancement. Empirical evidence demonstrates robust tumor suppression both in vitro and in vivo by the CeO2/Ti3C2-PEG-GOD nanocomposite. Consequently, this integrated approach, which combines PTT/PDT and enzymatic catalysis, could offer a valuable blueprint for the development of advanced oncology therapies.
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Small Methods
·
2025
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IF 9.1
Jinrui Li,Huiyan Xie,Di Sun,Hongguang Li,Xia Xin
Exploring potential third-order nonlinear optical (NLO) materials attracts ever-increasing attention. Given that the atomically precise and rich adjustable structural features of silver nanoclusters (Ag NCs), as well as the unique π-electron conjugated system of carbon-based nanomaterials, a supramolecular co-assembly amplification strategy to enhance the luminescent intensity and NLO performance of the hybrids of the two components, are constructed and the relationship between structures and optical properties are investigated. By combining water soluble Ag NCs [(NH 4 ) 6 [Ag 6 (mna) 6 ] (H 2 mna = 2-mercaptonicotinic acid, abbreviated to Ag 6 ─NCs hereafter) containing uncoordinated carboxyl groups with water-soluble fullerene derivatives modified with multiple hydroxyl groups (fullerenols, C 60 ─OH), the π-electron delocalization is expanded owing to non-covalent hydrogen bonding effect between Ag6─NCs and C 60 ─OH, which provides a feasible basis for realizing the NLO response. Then, the co-assemblies are doped into a PMMA matrix to prepare composite film and its NLO properties are evaluated by Z-scan technique. Remarkably, the effective nonlinear absorption coefficients β is of two orders magnitude higher than those of the Ag 6 ─NCs assemblies at the absence of C 60 ─OH. This work showcases a new approach for amplifying NLO responses which greatly facilitates the development of integrated photonic devices.
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JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY
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2025
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IF 4.9
Feifei Wang,Dianlong Jia,Qingcui Song,Xiaomeng Lu,Guozi Xia,Jun Li,Xiaodong Jia,Mingliang Gu,Fengjiao Yuan,Zhengping Wang,Zhangyong Xia
Resistance against tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced cell death of cancer cells is a major obstacle in clinical application of TRAIL. Bortezomib (BTZ) is the first-generation proteasome inhibitor to enhance TRAIL-mediated apoptosis and overcome tumor cell resistance to TRAIL, therefore we developed a novel nanodrug called LSBTZ-TRAIL to co-deliver TRAIL and BTZ via liposomes. TRAIL was coupled to the surface of the liposome by DSPE-PEG 2000 -NHS, while BTZ was encapsulated in the internal aqueous phase. LSBTZ-TRAIL was characterized with a particle size of 147.00 ± 1.300 nm, polydispersity index (PDI) of 0.056 ± 0.005 and zeta potential of -8.17 ± 0.600 mV. LSBTZ-TRAIL did not change the secondary structure of TRAIL, and LSBTZ-TRAIL was stable in 50% fetal bovine serum and tumor microenvironment. In vitro, the cell killing capacity of LSBTZ-TRAIL was 1.16-6.22 times that of TRAIL + BTZ. Mechanistically, LSBTZ-TRAIL induced apoptosis of tumor cells by up-regulating the death receptor (DR4/5) and activating the caspase signaling pathway. In vivo and in vitro uptake experiments, LS-TRAIL accumulated more in tumor cells or tissues than LS. In vivo , the antitumor effect of LSBTZ-TRAIL was 2.62 times that of TRAIL + BTZ, and prolonged the survival and blood circulation time of mice. In addition, safety evaluation showed that LSBTZ-TRAIL had no acute toxic effects in vivo . These results suggested that the liposomal co-delivery system of TRAIL and BTZ significantly enhance their antitumor effects and provide a new approach to overcome TRAIL-resistance.
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CARBOHYDRATE POLYMERS
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2024
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IF 10.7
Zhiyi Liao,Jiayi Li,Wenqiang Ni,Rixing Zhan,Xisheng Xu
Altered skin integrity increases the chance of infection, and bacterial infections often lead to a persistent inflammatory response that prolongs healing time. Functional artificial hydrogels are receiving increasing attention as suitable wound dressing barrier. However, the antimicrobial effect of the new dressing still needs to be explored in depth. In this work, the antimicrobial peptide MSI-1 was covalently attached to chitosan-modified poly (vinyl alcohol) hydrogels mixed with Prussian blue nanoparticles (PBNPs) via a primary amine group coupled to a carboxyl group. The synthesized hydrogel has a long-lasting antimicrobial surface and is able to maintain its bactericidal effect on Staphylococcus aureus and Escherichia coli for 24 h. Due to the presence of PBNPs, the hydrogel was able to rise to 48.3 °C within 10 min under near infrared (NIR) light irradiation at a wavelength of 808 nm and maintain this mild temperature to avoid bacterial biofilms. The hydrogel showed >90 % survival in co-culture with cells for 3 d and did not damage major organs in animal experiments. Thus, the photothermal dual-mode antimicrobial hydrogel synthesized in this study increases the selectivity as a safe and efficient wound dressing for the treatment of infected skin defects.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
Xue Yang,Yuxuan Wang,Jingxian Hua,Rujing Hou,Jinfeng Chen,Qihan Gong,Chongqing Wang,Yichang Pan
Plate-like or sheet-like porous materials with nanometer thickness have been considered as the preferred fillers to improve mixed-matrix membranes (mmms)-based separation. Herein, hexagonal Co-fa (HG-Co-fa) nanoplates were simply synthesized without the addition of any modifier and used as fillers to construct 6FDA-DAM-based MMMs for efficient CO 2 /CH 4 separation. HG-Co-fa nanoplates exhibit high dispersion and interface compatibility in 6FDA-DAM matrix. The results demonstrated that the CO 2 /CH 4 separation performance of 6FDA-DAM was obviously improved after the incorporation of HG-Co-fa nanoplates. The resultant MMMs with nanoplate loading of 10 wt% showed CO 2 /CH 4 selectivity of 27 and CO 2 permeability of 1419 Barrer at 25 ℃ and 0.2 MPa, surpassing 2008 Robeson upper bound. Meanwhile, the high lattice integrity and structural stability of HG-Co-fa nanoplates contribute to the excellent thermal and mechanical stability of MMMs, contributing to their anti-plasticization property up to 14 bar and long-term stability up to 240 h, indicating their potential for natural gas separation.
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Nature Communications
·
2025
·Vol. 16
·期 1
·1-14
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IF 15.7
Zhang Xiaoxin,He Hongyuan,Chen Yu,Yang Guangming,Xiao Xiao,Lv Haiping,Xiang Yongkang,Wang Shuxiong,Jiang Chang,Li Jianhui,Chen Zhou,Liu Subiao,Yan Ning,Yong Xue,Alodhayb Abdullah N.,Pan Yuanming,Chen Ning,Lin Jinru,Tu Xin,Shao Zongping,Sun Yifei
High-entropy LnBaCo 2 O 5+ δ perovskites are explored as rSOC air electrodes, though high configuration entropy ( S config ) alone poorly correlates with performance due to multifactorial interactions. We systematically engineer LnBaCo 2 O 5+ δ perovskites (Ln = lanthanides) with tunable S config and 20 consistent parameters, employing Bayesian-optimized symbolic regression to decode activity descriptors. The model identifies synergistic contributions from S config , ionic radius, and electronegativity, enabling screening of 177,100 compositions. Three validated oxides exhibit superior activity/durability, particularly (Pr 0.05 La 0.4 Nd 0.2 Sm 0.1 Y 0.25 )BaCo 2 O 5+ δ , showing enhanced oxygen vacancy concentration and disordered transport pathways. First-principles studies reveal optimized charge transfer kinetics via cobalt-oxygen bond modulation. Further, the interplay between first ionization energy, atomic mass, and ionic Lewis acidity dictates stability. This data-driven approach establishes a quantitative framework bridging entropy engineering and catalytic functionality in complex oxides.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2024
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IF 8.1
Haofan Jia,Liujing Yang,Hao Zhu,Yang Wang,Ying Chen,Kai Sun,Xinbao Li
In this study, a series of high-efficient catalyst, Co–Fe/Al 2 O 3 , were synthesized via the sol-gel method for low-temperature phenol steam reforming (PSR). The optimized catalyst, 15Co–2Fe/Al 2 O 3 , exhibited a remarkable phenol conversion of 95.3%, a H 2 yield of 92.1% at 450 °C, GHSV = 7500 h −1 and a steam-to-carbon (S/C) ratio of 10. Furthermore, the catalyst activity was maintained for 660 min before a gradual decline was observed. The NH 3 -TPD analysis revealed that the addition of Fe enhanced the surface acidity of the catalyst, providing more active sites for phenol adsorption and activation. This study aims to address the challenges associated with high reaction temperatures and poor catalyst stability in PSR. Various characterization techniques have been employed to investigate the reaction mechanisms of bimetallic catalysts in low-temperature PSR.
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CATALYSIS LETTERS
·
2024
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IF 2.3
Shen Nan,Hua Shaofeng
A dual-enzyme cascade catalytic system (Cu-rGO-Fe 3 O 4 -GA-CEL-PEI-GOD) was prepared by co-immobilizing cellulase (CEL) and glucose oxidase (GOD) on a nanocomposite (Cu-rGO-Fe 3 O 4 ) to efficiently catalyze the conversion of carboxymethyl cellulose (CMC) to gluconic acid. A layer-by-layer strategy was used by adding polyethyleneimine (PEI) to allow the upper enzyme layer to attach to the lower neighboring layer, increasing the loading capacity of the support. The loading capability of CEL and GOD on Cu-rGO-Fe 3 O 4 -GA-CEL-PEI-GOD were 55.034 mg g −1 and 12.4 mg g −1 , respectively. The specific activity of CEL on Cu-rGO-Fe 3 O 4 -GA-CEL was 74.3 U·g −1 , and that of immobilized CEL after cross-linking PEI was 25.45 U·g −1 , which could retain 34.253% of the enzyme activity. The specific activity of GOD on Cu-rGO-Fe 3 O 4 -GA-CEL-PEI-GOD was 30.9 U·g −1 . The carrier Cu-rGO-Fe 3 O 4 has peroxidase-like activity, which can timely remove harmful H 2 O 2 to the enzyme, thereby improving the yield of gluconic acid and the stability of biocatalysts. The yield of gluconic acid with Cu-rGO-Fe 3 O 4 -GA-CEL-PEI-GOD reached 96.04% within 2 h, higher than the control systems for comparison. In addition, the Cu-rGO-Fe 3 O 4 -GA-CEL-PEI-GOD maintained 82.61% of catalytic activity even after undergoing seven cycles of reaction. The dual-enzyme catalytic systems had shallow temperature and pH optima of 40 °C and 4.5. Such a chemoenzymatic cascade system provides a new strategy for the conversion from CMC to gluconic acid in one-step. Graphical Abstract Enzymatic conversion of sodium carboxymethyl cellulose (CMC-Na) to gluconic acid.
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Journal of Energy Storage
·
2024
·
IF 8.9
Fudong Jia,Ranshuo Zhang,Fangfang Wang,Chunxiao Jiao,Chao Gao,Jingjing Sang,Yanpei Xu,Qi Wang
With the increasing prevalence of mobile electronic devices, electric vehicles, and other technological advancements, there is a growing demand for higher-capacity Lithium-ion batteries (LIBs). Metal-organic frameworks (MOFs) have been actively researched in recent years due to their numerous advantages. However, the irreversible collapse during lithium-ion interaction hampers MOFs’ electrochemical stability. This study employs a direct precipitation method to synthesize uniformly shaped MOF materials, followed by carbon coating using electrospinning techniques , and ultimately, derivatives of MOF materials are produced through annealing. Thanks to this innovative material design process , exceptional performance is observed in this material as a lithium-negative electrode. After 1000 cycles at a high current density of 1 A g −1 , its reversible capacity stabilizes at 1318 mAh g −1 . Moreover, this negative electrode material exhibits exceptional rate performance at various current densities. The Co 3 O 4 /NiO@NCNFs electrode demonstrates enhanced charge storage capacity due to the synergistic effects of diffusion and capacitance control processes. Additionally, this material exhibits characteristics of low impedance and high lithium-ion diffusion rate. This study presents a novel method for manufacturing lithium-ion battery negative electrode materials by integrating MOF materials with electrospinning technology.
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ACS Applied Nano Materials
·
2025
·
IF 5.5
Huirong Chen,Jiamin Li,Zixin Huang,Yi Zhang,Yuee Ruan,Xiaonan Luo,Fengfeng Chen,Ruliang Liu
The increasing demand for sustainable and efficient catalytic processes has driven the development of advanced nanoreactors. In this study, we present a sophisticated Metal–organic framework (MOF)-template-mediated approach to synthesize yolk–shell Co-CN@SiO2 nanoreactors, where Co nanoparticles were supported on carbon nitride (C–N) nanosheets as the core encapsulated within a nanoporous SiO2 shell. This yolk–shell structure with confined cavities can provide a high surface area and overcome challenges such as Co nanoparticle sintering and mass transport limitations, resulting in superior catalytic performance. Remarkably, these nanoreactors achieved a 99% yield of benzyl alcohol from benzaldehyde hydrogenation under base-free conditions. Moreover, the influence of calcination temperatures on the structural evolution of the Co-based silica nanoreactors was explored, revealing the critical role of synergistic interaction between C–N and Co nanoparticles in boosting catalytic activity. Density functional theory calculations were conducted to investigate the adsorption energies of reacting species on the catalyst, providing mechanistic insights into the enhanced hydrogenation activity of the Co-CN@SiO2. This work offers valuable insights into the rational design of advanced nanoreactors for various catalytic applications, particularly in the field of green chemistry and sustainable synthesis.
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