JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
·
IF 6.3
Yong Zhou,Jiamei Liu,Xudong Zhao,Bin Yang,Bing Li,Xiaoyang Liu
Because of their unique electrical and magnetic properties, the perovskite multiferroic materials exhibit significant potential in spintronic device applications. However, synthesizing room-temperature multiferroic materials with robust magneto-electric coupling effects remains a major challenge. In this work, Yb 3 + , with an ionic radius slightly smaller than Y 3+ , was selected for A -site doping in the h -YMnO 3 , which has a high ferroelectric transition temperature (T C ∼ 900 K) and a low antiferromagnetic transition temperature (T N ≤ 70 K). This similar ionic radius allows Yb to substitute the Y site effectively while introducing distinct electronic states, thereby optimizing the structure and multiferroic properties of h -YMnO 3 without significantly altering the crystal structure. A series of Yb-doped Y 1- x Yb x MnO 3 ( x = 0, 0.1, 0.2, 0.3, 0.4, 0.5 and 1) materials were synthesized via conventional solid-phase reaction. The effects of Yb doping on the structure, magnetism, and ferroelectricity of h -YMnO 3 were studied. X-ray diffraction (XRD) and corresponding XRD refining results show that as Y 3+ is replaced by Yb 3+ with smaller radii, the cell parameters and cell volume of Y 1- x Yb x MnO 3 decrease, the cell is compressed, and the lattice structure of Y 0.5 Yb 0.5 MnO 3 obtained under the condition of Yb semi-doping changes significantly. Subsequent magnetic and room-temperature ferroelectric test results show that the Y 1- x Yb x MnO 3 series samples have anti-ferromagnetic ground states. In particular, the proper inclination of Mn 3+ ions in the double perovskite structure of Y 0.5 Yb 0.5 MnO 3 generates strong Dzyaloshinskii-Moriya (DM) interactions, resulting in relatively strong antiferromagnetism. The antiferromagnetic Neel temperature (T N ) from 37 K to 41 K. Yb 3+ -induced inclined ferroelectricity enables Y 0.8 Yb 0.2 MnO 3 to achieve the highest ferroelectric polarization of 0.030 µC cm −2 , which is 180 % greater than that of h -YMnO 3 . The results demonstrate that Yb doping plays a crucial role in regulating the structure and multiferroic properties of h -YMnO 3 , offering a novel strategy for developing room-temperature multiferroic materials with robust magneto-electric coupling.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Mengwei Han,Yuzhu Qian,Xinni Li,Nailiang Wang,Ting Song,Li Liu,Xianyou Wang,Xiongwei Wu,Man-Kay Law,Bei Long
Developing insertion-type anode is key to advancing “rocking chair” zinc-ion batteries, though there are few reported insertion-type anodes. Herein, the Bi 2 O 2 CO 3 is a high-potential anode, with a special layered structure. A one-step hydrothermal method was used to prepare Ni-doped Bi 2 O 2 CO 3 nanosheet , and also a free-standing electrode consisting of Ni-Bi 2 O 2 CO 3 and CNTs was designed. Both cross-linked CNTs conductive networks and Ni doping improve charge transfer. Ex situ tests (XRD, XPS, TEM, etc.) reveal the H + /Zn 2+ co-insertion mechanism of Bi 2 O 2 CO 3 and that Ni doping improves its electrochemical reversibility and structural stability. Therefore, this optimized electrode offers a high specific capacity of 159 mAh g −1 at 100 mA g −1 , a suitable average discharge voltage of ≈0.400 V, and a long-term cycling stability of 2200 cycles at 700 mA g −1 . Besides, the Ni-Bi 2 O 2 CO 3 //MnO 2 “rocking chair” zinc-ion battery (based on the total mass of cathode and anode) delivers a high capacity of ≈100 mAh g −1 at 50.0 mA g −1 . This work provides a reference for designing high-performance anode in zinc-ion batteries.
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CERAMICS INTERNATIONAL
·
2020
·
IF 3.83
Yunzi Li,Fei Chen,Xiaoyu Li,Qiang Shen,Lianmeng Zhang
Ceramic/metal composites, as high-temperature structural materials, have limited applications because of their poor machinability . AlN/Mo/Mo 2 B machinable composites were fabricated by adding h-BN to AlN/Mo composites by plasma-activated sintering at various temperatures and at an axial pressure of 30 MPa under argon atmosphere. The sample sintered at 1500 °C exhibited excellent machinability for cemented carbide tools, with a bending strength of approximately 500 MPa and a Vickers hardness value of 9.34 GPa. The effects of sintering temperature on the microstructure, mechanical properties, and machinability were investigated, and the reactions introduced by adding h-BN were studied. These reactions reinforced the composite and newly introduced a Mo 2 B phase, which showed better ability to deflect cracks and prevent them from moving deep inside the composite, thus improving its machinability. This research provides a possible solution for improving the machinability of ceramic/metal composites without sacrificing the strength .
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Journal of Energy Chemistry
·
2020
·
IF 7.216
Libin Wang,Ting Shu,Songtao Guo,Shi Chen,Yingjun Jiang,Xianluo Hu
ABSTRACT Owing to sluggish ionic mobility at low temperatures, supercapacitors , as well as other energy-storage devices, always suffer from severe capacity decay and even failure under extreme low-temperature circumstances. Solar-thermal-enabled self-heating promises an attractive approach to overcome this issue. Here, we report a unique H-bonding charge-transfer complex with a high photothermal conversion efficiency of 79.5% at 405 nm based on chloranilic acid and albendazole . Integrated with a microsupercapacitor, the chloranilic acid-albendazole complex (CAC) film prompts an apparent temperature increase of 22.7 °C under 1 sun illumination at −32.6 °C, effectively elevating the working temperature of devices. As a result, the rate capability of the microsupercapacitor has been significantly improved with a 17-fold increase in capacitance at a current density of 60 μA cm −2 , leading to outstanding low-temperature performances. Importantly, the integrated device is capable of working at a low temperature of −30 °C in the open air, which demonstrates the potential of CAC in practical applications for low-temperature ultracapacitive energy-storage devices.
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APPLIED ORGANOMETALLIC CHEMISTRY
·
2014
·Vol. 28
·期 9
·673-677
·
IF 2.017
Limin Ren,Wenyi Chu,Dinghui Guan,Yanjun Hou,Man Wang,Xiaobin Yuan,Zhizhong Sun
A simple and efficient route for the preparation of terphenyl derivatives via palladium-catalyzed sequential directed C―H arylation/Suzuki–Miyaura cross-coupling in ‘one-pot’ has been developed. 4,4′-(Cyclohexane-1,1-diyl)diphenol is an essential ligand. This reaction can tolerate a series of functional groups and provides the terphenyl derivatives in moderate to good yield. Copyright © 2014 John Wiley & Sons, Ltd.
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Journal of Building Engineering
·
2025
·
IF 7.4
Juanhong Liu,Yayun Xi,Fanghui Han,Lingzhi Guo,Jinmei Hu
This study investigates the influence of aluminum incorporation on the chemical composition, morphology, silicate chain structure, and functional groups of C(-A)-S-H gel through micro- and nanoscale characterization. Based on experimental data, an atomic-scale structural model was constructed to closely reflect realistic Ca/Si and Al/Si ratios as well as Q n distributions, and to explore the effects of aluminum content on the mechanical properties and failure mechanisms of C-A-S-H at the atomic level. Results show that at low Al/Si ratios, Al can be effectively incorporated into the C-S-H gel; however, when Al/Si exceeds 0.10, Al-containing secondary phases start to precipitate. Al atoms bridge defects in silicate chains, extend the length of aluminosilicate chains, and form crosslinking structures along the z direction, with the degree of crosslinking increasing with Al content. Simulation results further indicate that Al incorporation restricts the diffusion pathways of interlayer water molecules, thereby enhancing gel structural integrity. Meanwhile, the formation of a three-dimensional crosslinking network substantially improves mechanical performance, significantly increasing Young's modulus and tensile strength in the y and z directions—especially enhancing interlayer cohesion and ductility along the z direction . Under tensile loading, stress-induced hydrolysis and bond depolymerization accelerate bond cleavage and hydroxyl formation within the C-A-S-H.
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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
·
2018
·Vol. 18
·期 5
·3291-3298
·
IF 1.354
Yang Xi,Yu Xiaoyan,Naito Kimiyoshi,Ding Huili,Qu Xiongwei,Zhang Qingxin
A new thermally conductive and electrically insulative polyimide were prepared by filling different amounts of hexagonal boron nitride (h-BN) particles, and the thermal conductivity of Polyimide (PI) composites were improved with the increasing h-BN content. Based on this,
two methods were applied to improve thermal conductivity furtherly at limited filler loading in this paper. One is modifying the h-BN to improve interface interaction, another is fabricating a nano-micro hybrid filler with 2-D h-BN and 0-D nano-scale nanodiamond (ND) to build
more effective conductive network. Both surface modification and hybrid system have a positive effect on thermal conductivity. The composites introducing 40 wt% hybrid filler (the weight ratio of ND/modified BN was 1/10) showed the highest thermal conductivity, being up to 0.98 W/(m K) (5.2
times that of PI). In addition, the composites exhibits excellent electrical insulation, thermal stability properties etc.
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JOURNAL OF ORGANOMETALLIC CHEMISTRY
·
2021
·
IF 2.369
Ke Cao,Ji Wu,Cai-Yan Zhang,Li-Fang Ding,Junxiao Yang
A palladium catalyzed intramolecular amination of B(7)-H for synthesis of o -carborane fused isoquinolinones has been developed. Kinds of o -carborane fused isoquinolinones decorated with active groups have been synthesized with good to excellent yields. A plausible mechanism involving palladium catalyzed electrophilic B-H activation/amination was proposed.
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CERAMICS INTERNATIONAL
·
2026
·
IF 6
Yonghai Gou,Rui Zhang,Jun Pang,Zhenzhen Qiu,Chaochao Dong,Huidong Mo,Xiaoli Wu,Jilin Wang
Garnet transparent ceramics are promising color converters for white laser diodes (LDs) because of their efficient broadband emission and favorable thermal properties. Herein, composite color converters were prepared by integrating the Lu 3 Al 5 O 12 :Ce 3+ (LuAG:Ce) transparent ceramics with h-BN modified Mg 2 Al 4 Si 5 O 18 : Eu 2+ (MAS:Eu) phosphor-in-glass films (PiGFs). Under 450 nm excitation, the LuAG: Ce-BN-MAS:Eu composites exhibit broad emission bands ranging from 480 to 720 nm, and the relative Eu 2+ /Ce 3+ emission intensity ratio rises with increasing h-BN content. The optimized LuAG:Ce-2BN-MAS:3Eu sample shows the highest emission intensity, with an internal quantum efficiency of 92.46% and an external quantum efficiency of 42.83%. In addition, the emission intensity at 150 °C retains 94.56% of that at room temperature. Under blue-laser irradiation at 12.5 W∙mm -2 , the steady-state temperature of light spot remains below 76.7 °C. The constructed laser-driven lighting device exhibits a luminous efficacy of 83.45 lm∙W -1 , a correlated color temperature of 6103 K and a Ra of 85.8. These results indicate that the LuAG:Ce-BN-MAS:Eu composites exhibit great potential for high-color-rendering white LDs.
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Nature Communications
·
2025
·Vol. 16
·期 1
·1-11
·
IF 15.7
Liu Liangbin,Jin Lujie,Ren Renjie,Yan Wei,Fang Nan,Ji Yujin,Li Youyong,Zhuang Lin,Kong Qingyu,Hu Zhiwei,Shao Qi,Huang Xiaoqing
The development of highly active and CO-tolerant hydrogen oxidation reaction (HOR) electrocatalysts is of great significance for alkaline exchange membrane fuel cells (AEMFCs). Here, the designed atomically Ni anchored Ru/RuO 2 heterostructure nanosheets (Ni SA -Ru@RuO 2 NSs/C) exhibit enhanced activity and stability for HOR in alkaline media. The optimized electrocatalyst delivers a high CO-tolerant durability with 92.3% retention in the 1000 ppm CO concentration after 5000 s test. Moreover, the anode catalyst Ni SA -Ru@RuO 2 NSs/C assembled AEMFCs output a peak power density (PPD) and specific PPD of 1.76 W cm −2 and 17.6 W mg PGM −1 under the H 2 /O 2 condition and performed a long-term stability with negligible decay for 100 h at 0.5 A cm −2 for the AEMFCs. The relative mechanism studies reveal that the Ru/RuO 2 heterostructure nanosheet and dispersed Ni single atoms have optimized the *H and *OH adsorption simultaneously and weaken the *CO adsorption. Our work may offer a significant guideline on the rational design of high-performance HOR electrocatalyst for energy-related applications.
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CRYSTAL GROWTH & DESIGN
·
2026
·
IF 3.6
He-Mei Yin,Xin-Yu Sun,Ping Xu,Shu-Long Liu,Fu-Min Xue
Baloxavir marboxil (BXM), a novel oral antiviral drug, is classified as BCS II and suffers from bioavailability limitations due to its low solubility. To overcome these limitations, a cocrystallization strategy was adopted in the present study. It is noteworthy that no cocrystal form of BXM has been reported in the CSD database. This study reports the synthesis and comprehensive characterization of a novel baloxavir marboxil and probenecid (PRO) pharmaceutical cocrystal (BXM-PRO), which was designed to improve the dissolution performance of BXM for enhanced therapeutic efficacy. The single crystal was successfully prepared via slow evaporation from a mixed solvent of methanol and water and thoroughly characterized using single-crystal X-ray diffraction, powder X-ray diffraction, thermogravimetric and differential scanning calorimetry, Fourier transform infrared spectra, scanning electron microscopy, Hirshfeld surface analysis, and density functional theory calculations. Structural analysis confirmed the formation of a cocrystal stabilized by strong O–H···O hydrogen bonds. Subsequent evaluations included the powder dissolution rate, accelerated stability, and antiviral activity. The dissolution profiles revealed that the BXM-PRO cocrystal exhibits a significantly enhanced dissolution rate and higher solubility in both water and pH 6.8 buffer compared to pure BXM. Theoretical analysis suggests that strong hydrogen bonding between hydrogens of the O–H···O complexes plays a critical role in facilitating the improved dissolution performance of the cocrystal. Additionally, cytotoxicity assessment via CCK-8 assay indicated that the cocrystal possesses lower cytotoxicity against MDCK cells than BXM. The antiviral activity of the BXM-PRO cocrystals was compared with that of BXM alone as well as with that of physical mixtures of BXM with PRO in adequate stoichiometric ratios. Antiviral assays demonstrated that the cocrystal exhibits superior efficacy against the Yamagata strain, reduced effectiveness against H1N1 PR8 and H3N2 strains, and comparable activity against the Victoria strain relative to BXM alone. These findings indicate that the BXM-PRO cocrystal represents a promising strategy to enhance the solubility and bioavailability of BXM, with potential clinical benefits for the treatment of influenza virus infections.
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ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Shue Jin,Renli Yang,Chen Hu,Shiqi Xiao,Yi Zuo,Yi Man,Yubao Li,Jidong Li
The regeneration of oral tissues is a challenging clinical problem because of the complex microbial and biological stress environments. Electrospun fibrous scaffolds have attracted significant interest as effective barrier membranes for guided bone regeneration (GBR); however, no mature strategy yet exists for the surface modification of fibers to provide versatility to satisfy clinical requirements. This study demonstrated a practical biosafety strategy: the combined use of plant polyphenols and LL-37 peptides to modify the fiber surface to endow the fibrous scaffold with antimicrobial activity, immunoregulation, and vascularized bone regeneration. We confirmed that the LL-37 peptides interacted with tannic acid (TA) through noncovalent bonds through experiments and molecular docking simulation analysis. In vitro experiments showed that the TA coating imparted strong antibacterial properties to the fibrous scaffold, but it also caused cytotoxicity. The grafting of LL-37 peptide promoted the spreading, migration, and osteogenic differentiation of mesenchymal stem cells and was also conducive to the M2 polarization of RAW264.7 cells. In vivo experiments further verified that the LL-37 peptide-grafted fibrous scaffold significantly enhanced angiogenesis, anti-inflammatory effects, and type-H vascularized bone regeneration. Overall, the fibrous scaffold modified by the LL-37 peptide through TA grafting has significant potential for GBR applications.
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