CERAMICS INTERNATIONAL
·
2023
·
IF 5.2
Zhuojia Xie,Zhengguang Zou,Xinyu Jiang,Weijian Zhang
The effects of K + doping on structure, magnetic characteristics , magnetocaloric properties, and critical behavior of La 0.7-x Nd 0.1 Sr 0.2 K x Mn 0.95 Ni 0.05 O 3 (LNSKMNO) ceramics (x = 0.00, 0.05, and 0.10) were investigated. The X-ray diffraction and refinement findings revealed that LNSKMNO exhibited a distinctive rhombohedral structure of the R-3c space group (No. 167). To validate the chemical composition of LNSKMNO ceramics, EDS spectroscopy and X-ray photoelectron spectroscopy (XPS) were utilized. The magnetization of LNSKMNO exhibited a temperature-dependent behavior, revealing a phase transition from the ferromagnetic (FM) phase to the paramagnetic (PM) phase at approximately the Curie temperature (Tc). By utilizing normalization and Banerjee's criterion, the magnetic phase transition of LNSKMNO was determined to be a second order magnetic phase transition. The maximal magnetic entropy ( − Δ S M max ) of LNSKMNO around Tc was 4.24, 4.53, and 4.07 J/(kg K) at the 5 T external magnetic field (H). The Kouvel-Fisher approach and modified Arrott plot were used for determining the values of the critical exponents of β , γ , and δ . The critical exponents for LNSKMNO ceramics generally conformed to those obtained based on the Mean-field model.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2018
·Vol. 136
·期 2
·47016
·
IF 1.901
R. Wang,G. Ye,W. Zhou,F. Jiang,Y. Wu,J. Hou,D. Li,J. Wu,Y. Chang,A. Liang,J. Xu,Y. Du
The electron-donating substituted indole is generally difficult to be polymerized into high-quality film. The electrochemical polymerization of the electron-donating 3,4-ethylenedioxythiophene (EDOT)-monosubstituted indole may be a challenge. Herein, we designed and synthesized a novel fluorescent comonomer based on the combination of indole and EDOT groups, namely, 5-(2,3-dihydrothieno[3,4- b ][1,4]dioxin-5-yl)-1 H -indole (EDTI), and subsequently electrodeposited into flawless freestanding flexible poly(5-(2,3-dihydrothieno[3,4- b ][1,4]dioxin-5-yl)-1 H -indole) (PEDTI) film with a resistance of 60 MΩ/cm in CH 2 Cl 2 containing 0.1 M Bu 4 NBF 4 . Electrochemical results showed that the oxidation onset potential of EDTI was at 0.8 V vs Ag/AgCl, which was lower than those of indole (0.96 V vs Ag/AgCl) and EDOT (1.35 V vs Ag/AgCl). FTIR spectra indicated that the polymerization of EDTI occurred at the 5-position on thiophene ring and 2,3-positions on indole ring, forming the crosslinking polymer film. The colors of as-prepared PEDTI could switch reversibly from purple to brown under applied potentials of 1.3 and −1.3 V, which were distinctly different from those of polyindole, poly(3,4-ethylenedioxythiophene) (PEDOT), and poly(EDOT-bis-substituted indole) (PETI). Fluorescence spectral studies revealed that the comonomer and corresponding polymer were good blue-green light emitters. These results implied that PEDTI had potential applications for photoelectric devices such as electrochromic devices, light-emitting diodes, and fluorescence sensors. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 47016.
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高影响因子
Catalysis Science & Technology
·
2017
·Vol. 7
·期 18
·4007-4016
·
IF 5.773
Sen Liu,Guozhu Li,Yuying Gao,Zhourong Xiao,Junfeng Zhang,Qingfa Wang,Xiangwen Zhang,Li Wang
In this work, polydopamine (PDA)-coated multi-walled carbon nanotubes (CNTs) have been employed as reactive platforms for the anchoring of multiple heteroatom dopants. Single-, double-, and triple-doped CNTs with the elements N, S and B have been successfully prepared and systematically investigated as electrocatalysts for the oxygen reduction reaction (ORR). The obtained catalysts have been fully characterized by the nitrogen-adsorption technique, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Combining with the physicochemical properties of different doped CNTs and their catalytic performance, various doping modes are compared and the mechanism of these processes has been investigated. The synergetic effects on double and triple doped CNTs with N, S, and B are found. The new non-metal catalyst N–S–B-CNTs exhibits high electrocatalytic activity and good stability for ORR.
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高影响因子
ChemistrySelect
·
2023
·Vol. 8
·期 9
·e202203332
·
IF 2.1
Cunwei Qian,Ying Wang,Xian Li,Changsheng Yao
Graphical A convenient, rapid and electrochemical one-pot protocol is designed for the synthesis of pyrazolo[3,4- b ]quinolines derivatives. The reaction is carried out in an undivided cell equipped with an iron cathode and a graphite anode in the presence of sodium bromide as a supporting electrolyte. Fourteen pyrazolo[3,4- b ]quinoline derivatives are obtained under a constant current of 30 mA after 0.14 F/mol of electricity passed. A convenient, rapid and electrochemical one-pot protocol was developed successfully for the preparation of pyrazolo[3,4- b ]-quinoline derivatives. The reaction is carried out in a 25 mL three neck flask equipped with graphite electrode as anode and iron electrode as cathode (electrode area of 1 cm 2 ) with sodium bromide as supporting electrolyte at room temperature in ethanol. Fourteen pyrazolo-[3,4- b ]-quinoline derivatives were synthesized by use of various aldehyde (including aryl aldehydes and aliphatic aldehydes), dimedone and 5-amino-3-methyl-1-phenylpyrazole as substrates in good yields (76–86 %) with a constant current of 30 mA after 0.14 F/mol of electricity passed. All aimed products were characterized by IR, 1 H NMR and HRMS. Notably, the presented method features ecologically sound, simple experimental procedure and good yields.
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高影响因子
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
·
2014
·Vol. 2014
·期 14
·2917-2923
·
IF 3.154
Bo Xia,Guilin Cheng,Xianfu Lin,Qi Wu
Graphical A dynamic double kinetic resolution (DDKR) strategy under the co-catalysis of Raney nickel and Candida antarctica lipase B (CAL-B) was established for the one-pot simultaneous resolution of primary amines and secondary alcohols. Herein, we have established a dynamic double kinetic resolution (DDKR) strategy under the co-catalysis of Raney nickel and Candida antarctica lipase B (CAL-B) for the one-pot simultaneous resolution of primary amines and secondary alcohols (or esters). The DDKR strategy was successfully applied to the resolution of a series of racemic amines and secondary alcohols (or esters) as well as mexiletine, an important antiarrhythmic agent. The catalysts could be recycled and reused several times with the same high activity. Scale-up experiments were also successful. As a more atom-economical and efficient process than traditional simple kinetic resolutions, the DDKR strategy can be widely used to prepare optically pure amines and alcohols.
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高影响因子
SYNTHETIC METALS
·
2017
·
IF 2.435
Yuan Zhao,Xiaoliang Liu,Lu Lyu,Lin Li,Wenjun Tan,Shitan Wang,Can Wang,Dongmei Niu,Haipeng Xie,Han Huang,Yongli Gao
Modification by ultra-thin fullerene (C 60 ) insertion layer of about 1 monolayer on the electronic structure and the film growth of 2,7-diocty[1]benzothieno-[3,2-b]benzothiophene (C8-BTBT) on silicon oxide (SiO 2 ) is investigated using ultraviolet photoelectron spectroscopy (UPS), X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and X-ray diffraction (XRD). It is found that the ultra-thin C 60 insertion layer doesn’t induce an ambipolar charge transport characteristic but it indeed lifts up the energy levels of C8-BTBT, resulting in p-doping and hole accumulation at the semiconductor-dielectric interface. The charge transfer from trap states residing in the band gap of C8-BTBT to the lowest unoccupied molecular orbital (LUMO) of C 60 most likely leads to a decrease of threshold voltage for corresponding organic field effect transistors (OFETs) based on such a configuration. Band bending and decrease of the ionization potential (IP) are observed in the C8-BTBT film attributed to the increasing ordering of molecular orientation with the deposition of C8-BTBT. The HOMO downward shift is clearly bigger with the C 60 insertion layer than that without. A typical Volmer-Weber (VW) growth mode is detected due to the weaker van der Waals interaction between C8-BTBT and the underlying layer of C 60 /C8-BTBT than that between the C8-BTBT molecules. Compared to without C 60 interlayer, the molecular packing is a little more disordered at low coverages, resulting in more C8-BTBT molecules to lean away from the interface normal. The C8-BTBT film in such a structure phase has the HOMO closer to the E F than that at an almost perfectly vertically standing up configuration. Our results show that the introduction of C 60 insertion layer lifts up the HOMO of C8-BTBT and improves the energy level alignment at the interface.
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高影响因子
Small
·
2025
·
IF 12.1
Zhen Shi,Chenxi Fang,Jiaqian Li,Sateesh Bandaru,Muwen Liu,Lizhong Zhao,Xuefeng Zhang
In spite of superior magnetic properties, neodymium–iron–boron (Nd-Fe-B) applications in harsh environments have been greatly hindered by their susceptibility to corrosion, humidity, mechanical, and temperature attacks. Herein, a construction strategy of robust slippery liquid-infused porous surfaces (SLIPS) coatings is proposed via the multi-dimensional design of surface, bulk coating, and interface. The manipulation of colloidal states of silica particles by chemical hydrophobization allows for building a dense polymer network, enhancing interfacial adhesion and locking lubricant film effectively. The resulting coating is demonstrated to be extremely stable, endowing the magnet with excellent liquid repellency, anti-corrosion, and anti-icing properties. Strikingly, no trace of corrosion is detected after 136-day immersion in 3.5 wt.% NaCl solution and the impedance modulus at 0.1 Hz can be maintained as the initial of 3.31 × 10 8 Ω·cm 2 even after 132-day immersion, which is far superior to that of commercial Ni-Cu-Ni, Zn, and EP coatings. Additionally, anti-icing performance at low temperatures is evidenced by the delayed icing time and decreased ice adhesion strength. Importantly, the self-healing property offers the surface intensified durability even after mechanical damage. This work demonstrates a construction strategy of robust SLIPS coatings with a multi-dimensional design, enabling the practical applications of Nd-Fe-B magnets in extreme environments like offshore wind turbines.
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产品关联
DOI
PubMed
高影响因子
POLYMER
·
2020
·
IF 4.231
Chandra Sekhar Biswas,Arpan Biswas,Massimillano Galluzzi,Mehdihasan I. Shekh,Qiao Wang,Biswajit Ray,Pralay Maiti,Florian J. Stadler
The synthesis of amphiphilic block-copolymers of poly( N -isopropylacrylamide) (PNIPAM) and poly( N -acryloyl- l -phenylalanine methyl ester) (PNALPA) by RAFT polymerization is reported. The polymers were characterized by proton NMR ( 1 H NMR), gel permeation chromatography (GPC), powder X-ray diffraction (XRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) to understand their structure-property relationships. All synthesized polymers show pH triggered release at acidic (pH 5) and biological pH (pH 7.4). Critical micellar concentration also varied systematically depending on the amphiphilic nature of the polymers. Biocompatibilities of the polymers are also determined to check their suitability for biomedical applications.
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高影响因子
Desalination and Water Treatment
·
2024
·
IF 1
Huali Zhang,Jiaxin Zhang,Hanjun Wu,Yi Pan,Yan Xia,Zhiquan Pan,Dongshen Wang
In this work, heterogeneous catalysts of Cu(II)-ethylenediamine tetramethylene phosphonic acid (Cu(II)-EDTMPA) complex intercalated layered double hydroxides (EDTMPA-Cu-LDH) was synthesized by co-precipitation method for visible-light photocatalytic degradation of Rhodamine B (RhB). The synthesized catalysts were characterized by X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, UV-Vis diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy. The results indicated that the EDTMPA-Cu-LDH showed a typical layered structure. After intercalation, layer spacing increased from 7.96 to 12.21 Å. The catalysts showed excellent catalytic activity for the degradation of RhB in visible light. The optimum conditions for RhB degradation were confirmed to be natural initial pH value 5.85, 10 mmol L –1 of RhB concentration, 7 mmol L –1 of H 2 O 2 concentration, and 0.3 g L –1 of catalyst dosage. The maximum degradation efficiency was 98.2% under the optimum conditions and excellent reusability and stability were obtained in the regeneration test. In the end, the reaction mechanism that might exist in the heterogeneous UV-Fenton system was proposed.
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高影响因子
BIOMEDICINE & PHARMACOTHERAPY
·
2024
·
IF 6.9
Qin Lihao,Liu Tingting,Zhang Jiawei,Bai Yifei,Tang Zheyu,Li Jingyan,Xue Tongqing,Jia Zhongzhi
In patients with diabetic wounds, wound healing is impaired due to the presence of persistent oxidative stress, an altered inflammatory response, and impaired angiogenesis and epithelization. Salvianolic acid B (SAB), which is derived from the Chinese medicinal plant Salvia miltiorrhiza , has been found to exhibit antioxidant, anti-inflammatory, and proangiogenic effects. Previous studies have used 3D bioprinting technology incorporating sodium alginate (SA) and gelatin (Gel) as basic biomaterials to successfully produce artificial skin. In the current study, 3D bioprinting technology was used to incorporate SAB into SA-Gel to form a novel SAB-SA-Gel composite porous scaffold. The morphological characteristics, physicochemical characteristics, biocompatibility, and SAB release profile of the SAB-SA-Gel scaffolds were evaluated in vitro. In addition, the antioxidant, anti-inflammatory, and proangiogenic abilities of the SAB-SA-Gel scaffolds were evaluated in cells and in a rat model. Analysis demonstrated that 1.0 wt% (the percentage of SAB in the total weight of the solution containing SA and Gel) SAB-SA-Gel scaffolds had strong antioxidant, anti-inflammatory, and proangiogenic properties both in cells and in the rat model. The 1.0% SAB-SA-Gel scaffold reduced the expression of tumor necrosis factor-α, interleukin-6, and interluekin-1β and increased the expression of transforming growth factor-β. In addition, this scaffold removed excessive reactive oxygen species by increasing the expression of superoxide dismutase, thereby protecting fibroblasts from injury. The scaffold increased the expression of vascular endothelial growth factor and platelet/endothelial cell adhesion molecule-1, accelerated granulation tissue regeneration and collagen deposition, and promoted wound healing. These findings suggest that this innovative scaffold may have promise as a simple and efficient approach to managing diabetic wound repair.
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PubMed
高影响因子
FUEL
·
2025
·
IF 7.5
Jingting He,Kun Yang,Guisheng Qi,Zonglin Yi,Yujing Guo,Qiang Guo
Electrocatalytic nitrate reduction reaction (NO 3 RR) represents a promising approach for regulating the global nitrogen cycle and serves as a crucial complementary method for ammonia synthesis. However, NO 3 RR is a complex reduction process involving the transfer of eight electrons and nine protons. Therefore, it is difficult for catalysts with a single catalytic site to maintain an advantage throughout the NO 3 RR process. Consequently, the fabrication of catalysts with synergistic effects to achieve both high efficiency and selectivity remains a formidable challenge. Herein, a simple precipitation-calcination process was employed to successfully introduce boron (B) and nickel (Ni) elements into Co 3 O 4 (B/Ni-Co 3 O 4 ) simultaneously. Impressively, the as-prepared B/Ni-Co 3 O 4 catalyst exhibited a remarkable NH 3 yield of 17.2 mg·h −1 ·mg cat −1 and a high FE of 97.2 % at −0.5 V relative to the reversible hydrogen electrode (RHE). Density functional theory (DFT) computations uncovered a cooperative effect between B and Ni dopants, specifically: B doping exhibited appreciable efficacy in NO 3 – adsorption, and the Ni dopant showed notable activity in promoting the conversion of NO 2 − . Further DFT calculations identified the *NO → *NOH step as rate-determining and revealed that B-Ni co-doping diminishes its thermodynamic energy barrier. Concurrently, experimental measurements showed that such co-doping lowers the onset potential to −0.06 V vs. RHE. This dual doping strategy significantly accelerates the electroreduction of NO 3 − to NH 3 .
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产品关联
DOI
高影响因子
ADVANCED SYNTHESIS & CATALYSIS
·
2011
·Vol. 353
·期 5
·713-718
·
IF 5.25
Ruiping Wang,Song Mo,Yongzhong Lu,Zengming Shen
Both indoles and benzo[ b ]furans can be obtained in high yield by the reactions of 2-iodoaniline derivatives and 2-iodophenols with terminal alkynes under mild conditions, namely in the presence of cuprous iodide (10 mol%) and a base in ethanol or 1,4-dioxane. Further investigation reveals that palladium contaminants as low as 100 ppb are responsible for these successful couplings. It is worth noting that simple aliphatic substituted terminal alkynes could be tolerated to smoothly produce indole and benzo[ b ]furan derivatives.
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高影响因子
危险品化学品经营许可证（带存储）