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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2024 ·Vol. 107 ·期 10 ·6833-6843 · IF 3.5

Improved piezoelectric properties in Bi(Mg2/3Nb1/3)O3-modified BiFeO3–BaTiO3 lead-free piezoelectric ceramics

Hailan Qin,Jianwei Zhao,Xiaoxin Chen,Hongtian Li,Shenghao Wang,Yuxiao Du,Ahmad Azmin Mohamad,Huanfu Zhou,Dawei Wang

The investigation of lead-free ceramics with exceptional piezoelectric properties holds great importance in the substitution of lead-based materials, hence promoting the development of green technology and fostering an environmentally sustainable society. This study successfully synthesized two series of Bi(Mg 2/3 Nb 1/3 )O 3 (BMN)-modified BiFeO 3 –BaTiO 3 (BF–BT) lead-free piezoelectric ceramics using the conventional solid-state reaction approach. The phase structure, microstructure, dielectric, and piezoelectric properties of these ceramics were comprehensively investigated. A typical perovskite structure is observed in all probed compositions, and the associated phase structure undergoes a gradual transition from a rhombohedral-cubic phase mixture to a cubic-dominant phase structure as increases the content of BMN and BT. All compositions exhibit obvious core–shell microstructures with inhomogeneous element distributions. Most importantly, the BF–0.30BT–0.005BMN and BF–0.34BT–0.03BMN piezoelectric ceramics presented remarkable values for the piezoelectric coefficient (225 pC/N) and converse piezoelectric coefficient (396 pm/V), respectively. These findings highlight the potential of BMN-modified BF–BT ceramics for use in high-performance piezoelectric applications.

研究领域: 材料科学 · 物理学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

A polysaccharide from Gynostemma pentaphyllum: structure characterization and anti-insulin resistance potential through Galectin-3 modulation

Mingwang Ren,Guoqing Sun,Xiaoyu Ding,Xiaolin Yu,Li He,Shiji Xiao,Minjian Dong,Jianwen Yang,Kan Ding,Chengxin Sun

Polysaccharides are among the key bioactive components of Gynostemma pentaphyllum (Thunb.) Makino . In this study, a novel polysaccharide fraction, GPPA1-1, was isolated from G. pentaphyllum and purified using DEAE-Sepharose Fast Flow, Sephadex G-75, and Sepharose CL-6B column chromatography. GPPA1-1 was determined to have a molecular weight of 3.7 × 10 4  Da and was composed of mannose (Man), glucuronic acid (GlcA), rhamnose (Rha), glucose (Glc), galactose (Gal), and arabinose (Ara) in a molar ratio of 3.88:3.97:21.77:7.02:45.65:17.71. Comprehensive structural characterization was conducted using Congo red staining, FT-IR spectroscopy, Methylation analysis, and NMR analysis. The backbone of GPPA1-1 was identified as comprising →4)-α-Gal p- (1→, →4)-α-Gal p- (3,1→, →2)-α-Rha p- (4,1→, and →2)-α-Rha p- (1→, with branch chains containing α-Ara f -(1→, →5)-α-Ara f -(1→, →3)-α-Galp-(1→, and -α-GlcA-(1→. Biological assays demonstrated that GPPA1-1 effectively alleviates insulin resistance by inhibiting Galectin-3. This activity was confirmed through various experiments, including Galectin-3-mediated hemagglutination, Western blotting, CETSA, and glucose uptake assays. These findings highlight the potential of GPPA1-1 as a promising therapeutic agent for managing insulin resistance.

CAS / MDL: 15681-89-7
研究领域: 植物化学 · 代谢生物学 · 药理学
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TETRAHEDRON · 2017 · IF 2.651

Metal-free visible-light-promoted intermolecular [2+2]-cycloaddition of 3-ylideneoxindoles

Ling-Ling Wu,Gao H. Yang,Zhi Guan,Yan-Hong He

The Rose Bengal sensitized intermolecular [2 + 2]-cycloaddition of 3-ylideneoxindoles for the synthesis of spirocyclic oxindoles was developed successfully under visible light irradiation conditions. The cycloaddition products were obtained in good yields (up to 93%) with excellent diastereoselectivity and regioselectivity by using a low loading of Rose Bengal (0.125 mol%) as a triplet sensitizer. This work demonstrates the potential benefits of Rose Bengal in visible light catalysis.

CAS / MDL: 632-69-9
研究领域: 有机化学 · 光化学
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INTEGRATED FERROELECTRICS · 2021 · IF 0.836

Realizing Hybrid Ion Storage of NASICON-Structured Na3V2(PO4)3 Prepared by Microwave Irradiation Route

Ji Yan,Zhen Li,Xiao-Kai Ma,Xin-Bo Chang,Fu-Jun Liu,Yong Zhang,Li-Zhen Wang

NASICON Na3V2(PO4)3 was investigated as cathode material in hybrid ion batteries using Li as counter and LiPF6 as electrolyte. The highly efficient and homogeneous heating merits of microwave irradiation facilitates the Na3V2(PO4)3 achieving excellent crystal structure, uniform carbon coating, as well as ideal particle size. After microwave irradiation, a specific capacity of 96.5 mAh g−1 is obtained for the first intercalation of lithium ion into Na3V2(PO4)3 at 0.1 C rate. For long-term cycling stability, the capacity retention reaches 84.4% at 5 C rate after 500 cycles. The unique intercalation/extraction characteristic promises Na3V2(PO4)3 an ideal candidate material for next-generation hybrid ion storage system.

研究领域: 材料科学 · 电化学
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MICROCHIMICA ACTA · 2019 ·Vol. 186 ·期 6 ·1-7 · IF 5.479

Fluorometric determination of copper(II) by using 3-aminophenylboronic acid-functionalized CdTe quantum dot probes

Xiong Huayu,Wang Bei,Wen Wei,Zhang Xiuhua,Wang Shengfu

Water-soluble cadmium telluride quantum dots capped with 3-mercaptopropionic acid were synthesized and further modified with 3-aminophenylboronic acid to form boronic acid-functionalized quantum dots (QDs). Under excitation at 350 nm, the modified QDs display yellow fluorescence with a peak at 566 nm. On exposure to copper(II), the fluorescence of the QDs is quenched. Under optimal conditions, fluorescence drops linearly in the 0.01 to 20 μM Cu(II) concentration range, and the detection limit is 7.6 nM. This fluorescent probe was applied to the determination of Cu(II) in spiked human serum and water samples and gave satisfactory results. Schematic presentation of the principle for fluorometrice detection of copper(II) based on the use of boronic acid-functionalized cadmium telluride quantum dots (CdTe QDs).

研究领域: 分析化学 · 材料科学 · 环境科学
✓ 已验证 DOI PubMed 高影响因子
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ChemSusChem · 2021 ·Vol. 14 ·期 16 ·3382-3390 · IF 8.928

Amorphous Fe(OH)3 Passivating CeO2 Nanorods: A Noble-Metal-Free Photocatalyst for Water Oxidation

Ting Feng,Jing Ding,Haiyan Li,Wei Wang,Bohua Dong,Lixin Cao

Graphical In hot water : CeO 2 /A−Fe(OH) 3 composites synthesized by a secondary water bath at 100 °C exhibit superior photocatalytic activity. A−Fe(OH) 3 increases specific surface area, passivates the surface of CeO 2 , and reduces the activation energy of water oxidation. This work provides a new insight into exploring amorphous cocatalysts to enhance photocatalytic O 2 evolution activity and augment the possibility of overall water splitting based on CeO 2 . Noble-metal-free composites with good photocatalytic property are of great interest. Here, CeO 2 nanorods composites loaded with amorphous Fe(OH) 3 cocatalyst were designed and prepared via a secondary water bath at 100 °C. The as-synthesized CeO 2 /amorphous Fe(OH) 3 composites exhibited superior light photocatalytic activities compared to pure CeO 2 , especially the sample with a loading time of 60 min. The photocatalytic oxygen generation rate could reach to 357.2 μmol h −1 g −1 , and the average apparent quantum yield (AQY) was 24.67 %, which was a 5.5-fold increase compared to the CeO 2 sample. The improvement of photocatalytic performance could be ascribed to three main reasons: First, loading the amorphous Fe(OH) 3 enlarged the specific surface area and passivated the surface of the pristine CeO 2 . Second, the amorphous Fe(OH) 3 ,which acted as a cocatalyst, provided many active sites, and reduced the reaction activation energy. Thirdly, the maximum interface with intimate contact between CeO 2 and amorphous Fe(OH) 3 cocatalyst accelerated the photogenerated charge separation efficiency and thus improved the photocatalytic performance of CeO 2 in photocatalytic water oxidation.

研究领域: 材料科学 · 环境科学 · 化学
✓ 已验证 DOI PubMed 高影响因子
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BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT · 2022 · IF 1.762

Protein engineering of CMP kinases to improve thermal stability and resultant production of 3′-sialyllactose

Jingjing Wang,Jinyong Wu,Zhongkui Li,Xiangsong Chen,Weiwei Liu,Jianming Yao

Protein engineering is an effective method to improve the thermal stability of biological macromolecules. Cytidine monophosphate kinase (CMK) is a key enzyme involved in nucleotide metabolism and participates in the production of cytidine triphosphate. It has previously been confirmed that CMK shows low thermal stability. This study aimed to enhance the thermal stability of CMK. Herein, we first analyzed native CMK using PoPMuSiC. Thereafter, we constructed single point mutants (Q30G, P62R, E85I, D148W and K165L) and multipoint mutants of CMK with higher thermal stability using site-directed mutagenesis. The thermal stability of the mutant Q30G/E85I/K165L was observed to be 1.2-fold higher than that of the wild type. The mutants were then allowed to catalyse 3′-sialyllactose (3′-SL) synthesis. After 51.72 mmol/L N-acetylneuraminic acid (sialic acid) was consumed in a 25 mL reaction system and 50.67 mmol/L 3′-SL was obtained, a decrease of 2 h was recorded in the reaction time, whereas the yield rate increased by 33.6%. The results suggest that the mutant Q30G/E85I/K165L can improve the thermal stability of CMK and its catalytic efficiency for 3′-SL synthesis. These findings are crucial for various applications involving enzyme conversion.

CAS / MDL: 56-65-5
研究领域: 生物化学 · 蛋白质工程 · 食品科学
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NANOTECHNOLOGY · 2023 ·Vol. 34 ·期 13 ·135601 · IF 3.5

Cr(OH)3 nanosheets@ZIF67 electrocatalysts prepared by electrodeposition method for efficient oxygen evolution reaction

Yudan Chai,Xuedong Wei,Yufen Wang,Shuangyan Qiao

In this paper, a Cr(OH)3 NSs@ZIF67 (NSs = nanosheets) electrocatalyst is prepared on foam Ni via a simple and rapid electrochemical deposition method. Excellent electrocatalytic activity of Cr(OH)3 NSs@ZIF67 is demonstrated. It can use the overpotential of 281 mV and 390 mV respectively to drive 10 mA cm−2 and 50 mA cm−2. It is observed that the Cr(OH)3 NSs@ZIF67 electrode has the highest initial current density at 1.57 V compared with the other two monomer electrodes and shows excellent stability at the end of 60 000 s. It has the largest electrochemical activity specific surface and lowest charge-transfer resistance, and M–O bonds (M = Co, Cr) and shifting of binding energy peaks at the interface lead to more active sites and more efficient electron transfer for oxygen evolution reaction. This work highlights the construction of highly efficient composite electrocatalysts composted of low-dimensional non-precious transition metal compounds and metalorganic frameworks, promoting the development of low-cost non-noble metal composites in energy chemistry.

研究领域: 材料科学 · 电化学
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Frontiers in Chemistry · 2022 · IF 5.545

Structural Characterization and Anticoagulant Activity of a 3-O-Methylated Heteroglycan From Fruiting Bodies of Pleurotus placentodes

Yin Zhen-Hua,Liu Xiao-Peng,Wang Jin-Mei,Xi Xue-Feng,Zhang Yan,Zhao Rui-Lin,Kang Wen-Yi

Pleurotus placentodes, a fungus, belongs to the Pleurotaceae family. The aim of the present study was to characterize the structure of a novel polysaccharide from fruiting bodies of P. placentodes (PPp-W) and evaluate its anticoagulant activity in vitro. The high-performance liquid chromatography and GC–MS analysis indicated that PPp-W with a molecular weight of 27.4 kDa was mainly composed of mannose (17.56%), glucose (6.37%), galactose (44.89%), and fucose (1.22%) with a certain amount of 3-O-methyled galactose. SEM, XRD, and AFM combined with Congo red test revealed that PPp-W was an irregular curly sheet with triple-helix conformation. The FT-IR, methylation, and nuclear magnetic resonance analysis indicated that PPp-W contained→6)-α-D-Galp-(1→, →6)-3-O-Me-α-D-Galp-(1→and →2, 6)-α-D-Galp-(1→ as main chain, partially substituted at O-2 and O-6 by non-reducing ends of β-D-Manp-(1→ and β-L-Fucp-(1→ with a small amount of α-1,3-linked-Glcp in backbone. PPp-W could significantly prolong APTT (12.9 ± 0.42 s, p < 0.001) and thrombin time (39.9 ± 0.28 s, p < 0.01) compared with the control group (11.45 ± 0.071 s and 38.05 ± 0.21 s), which showed that PPp-W had anticoagulant activity. These studies suggested that PPp-W was a 3-O-methylated heteroglycan and might be suitable for functional foods and natural drugs as an anticoagulant ingredient, which provided a basis for the application of polysaccharides from P. placentodes.

研究领域: 真菌学 · 生物化学 · 药理学
✓ 已验证 DOI PubMed 高影响因子
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International Journal of Electrochemical Science · 2024 · IF 1.3

Phosphorus doping heterostructure La(OH)3@CuO @NF as an advanced electrocatalyst for the oxygen evolution reaction

Dandan Liang,Weili Hou,Ying Zhang,Jihua Shang,Haibo Ren,Yufeng Sun

Due to the prevailing energy shortages, the pursuit of new alternative energy sources is becoming increasingly urgent. Hydrogen production through water electrolysis has emerged as a crucial method. However, the sluggish four-electron reaction in the oxygen evolution reaction (OER) remains the primary rate-limiting step. In this study, we synthesized a heterostructure La(OH) 3 @CuO-P material on the nickel foam (NF) substrate. The experimental results demonstrate that after phosphating treatment, the heterostructure La(OH) 3 @CuO-P exhibits exceptional catalytic performance with only 215 mV overpotential, a Tafel slope value of 79.36 mV/dec, and a bilayer capacitance of 39.02 mF/cm 2 at a current density of 10 mA/cm 2 for OER in a 1 M KOH solution. These values are significantly superior compared to those obtained using heterostructure La(OH) 3 @CuO alone which showed an overpotential value of 365 mV at a current density of 10 mA/cm 2 . Moreover, during cyclic voltammetry testing for up to 500 cycles, La(OH) 3 @CuO-P also demonstrates relatively stable performance. Analyses suggest that composite heterostructure effectively addresses issues such as insufficient conductivity of La(OH) 3 and monomer aggregation tendency for CuO while maintaining excellent properties for each component. By incorporating P atoms as dopants, the interaction between La, Cu, and P atoms not only facilitates fine-tuning of the electronic structure and optimization of the adsorption free energy (-OH), but also promotes an increase in catalytic active sites through sample size reduction, thereby further augmenting the performance of the OER.

CAS / MDL: 10031-43-3 10277-43-7
研究领域: 材料科学 · 电催化
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Preparation of large layered MXene/Al(OH)3 composite membranes with porous structures and efficient separation performance

Peng Zu,Haoning Li,Guangming Yan,Gang Zhang

In this study, Ti 3 C 2 T x layers with an average lateral size of approximately 8.3 μm were prepared. The LLM composite membranes synthesized from these layers not only possessed long and narrow mass transfer channels but also further prevented the generation of internal non-selective defects. Additionally, a strategy of compositing these Ti 3 C 2 T x layers and Al(OH) 3 was adopted. The strategy contributed to expanding the interlayer distances of the composite membranes and adjusting the in-plane stacking order, thereby facilitating the construction of mass transfer channels characterized by high permeance within the membranes. This resulted in the preparation of LLMA membranes. Among these LLMA membranes, the LLMA-1:7 composite membranes displayed outstanding performance in the sieving process. Their permeances were more than 10 times higher than those of the LLM membranes (with a thickness of 1 μm). Also, the rejection ratio for CV dye could even exceed 99 %, and the operational stability was also significantly improved. These advantages enabled them to avoid some of the shortcomings commonly found in two-dimensional (2D) separation membranes to a certain extent. In summary, the LLMA-1:7 composite membranes designed in this study demonstrated superior overall performance, compared to the majority of the previously reported 2D membranes. This research is expected to establish a solid foundation for the application of 2D MXene membranes in the field of water treatment.

研究领域: 材料科学 · 环境工程
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Polymers · 2023 ·Vol. 15 ·期 1 ·248 · IF 5

Controllable Preparation of Superparamagnetic Fe3O4@La(OH)3 Inorganic Polymer for Rapid Adsorption and Separation of Phosphate

Yao Lu,Xuna Jin,Xiang Li,Minpeng Liu,Baolei Liu,Xiaodan Zeng,Jie Chen,Zhigang Liu,Shihua Yu,Yucheng Xu

Superparamagnetic Fe3O4particles have been synthesized by solvothermal method, and a layer of dense silica sol polymer is coated on the surface prepared by sol-gel technique; then La(OH)3covered the surface of silica sol polymer in an irregular shape by controlled in situ growth technology. These magnetic materials are characterized by TEM, FT-IR, XRD, SEM, EDS and VSM; the results show that La(OH)3nanoparticles have successfully modified on Fe3O4surface. The prepared Fe3O4@La(OH)3inorganic polymer has been used as adsorbent to remove phosphate efficiently. The effects of solution pH, adsorbent dosage and co-existing ions on phosphate removal are investigated. Moreover, the adsorption kinetic equation and isothermal model are used to describe the adsorption performance of Fe3O4@La(OH)3. It was observed that Fe3O4@La(OH)3exhibits a fast equilibrium time of 20 min, high phosphate removal rate (>95.7%), high sorption capacity of 63.72 mgP/g, excellent selectivity for phosphate in the presence of competing ions, under the conditions of phosphate concentration 30 mgP/L, pH = 7, adsorbent dose 0.6 g/L and room temperature. The phosphate adsorption process by Fe3O4@La(OH)3is best described by the pseudo-second-order equation and Langmuir isotherm model. Furthermore, the real samples and reusability experiment indicate that Fe3O4@La(OH)3could be regenerated after desorption, and 92.78% phosphate removing remained after five cycles. Therefore, La(OH)3nanoparticles deposited on the surface of monodisperse Fe3O4microspheres have been synthesized for the first time by a controlled in-situ growth method. Experiments have proved that Fe3O4@La(OH)3particles with fast separability, large adsorption capacity and easy reusability can be used as a promising material in the treatment of phosphate wastewater or organic pollutants containing phosphoric acid functional group.Keywords:superparamagnetic;Fe3O4@La(OH)3inorganic polymer;phosphate adsorption

研究领域: 材料科学 · 环境科学
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