JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2022
·Vol. 33
·期 22
·17814-17827
·
IF 2.779
Liu Zhuofeng,Liang Wenxue,Zhang Weijun,Wang Fenglin,Xun Yan,Chen Tongting,Li Wei,Chen Xingyu,Mao Haijun
The co-firing compatibility between green tape and the Ag electrode is a crucial characteristic in low-temperature co-fired ceramic (LTCC) technology and plays a vital role in improving the performance and application status of LTCC device modules. In this work, we studied the effects of lead content on the glass viscosity, the microstructure, and co-firing compatibility of silver electrode film. It was found that the softening point and viscosity of the glass were decreased, and the wettability between the glass and silver was improved with the increase of the lead content, which promoted the co-firing densification and interfacial bonding between the silver electrode film and the ceramic layer. The film presented the best electrical properties co-firing at 875 °C for 15 min, with the resistivity of 1.21 mΩ/sq. And the film was densified. The sintering interface was clear and well bonded. The results showed that an appropriate lead content in glass could effectively improve the interfacial bonding and the electrical properties during co-fired process, providing a new control methodology for realizing co-fired matching of the silver electrode film with low-temperature co-fired ceramics.
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DOI
高影响因子
DYES AND PIGMENTS
·
2018
·
IF 3.767
Xueyan Wu,Jixi Guo,Wei Jia,Jianzhang Zhao,Dianzeng Jia,Huici Shan
A facile and efficient method is described to greatly improve the emission efficiency of anthracene- o -carborane dyad by linking two o -carborane building blocks together through tailored alkyl linkages. Improvement of the emission efficiency of the tethered anthracene- o -carborane dyads was achieved with the quantum yield up to 40.8% and 51.4% for BCAC4 and BCAC6 respectively, in contrast to that of CAH (4.3%) and CAA (36%), demonstrating that the cooperation advocates that one plus one is much bigger than two. In addition, these developed emissive AIE luminogens exhibit impressive response to the environmental stimuli of viscosity and temperature. DFT calculations were carried out to explore the influence of the anthryl and alkyl linkages on emission efficiency. Our materials and concepts are useful as a guideline for designing o -carborane-containing highly-efficient solid luminescent materials with stimuli-responsive properties.
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DOI
高影响因子
Catalysis Science & Technology
·
2021
·Vol. 11
·期 21
·7200-7216
·
IF 6.119
Hairus Abdullah,Hardy Shuwanto,Dong-Hau Kuo
A Ni–Mg bimetal-doped Zn(O,S) photocatalyst has been synthesized, characterized, and tested for several photocatalytic applications. The hydrogen generation reaction, hydrogenation reaction for chemical transformation, detoxification of hexavalent chromium, and mixed dye (MB + RhB + MO) degradation under simulated solar-light illumination were confirmed. The essential characterization results indicated improved oxygen vacancy sites on the catalyst with enhanced photoresponse, better photocarrier separation, and facile charge transfer properties. A typical catalyst, NMZ-S10, was evaluated with a 1000-cycle CV test to demonstrate its long-term use for industrial application. Stable reusability experiments for the HER, PHR, PHC reaction, and PDM also supported the long-term application. The photocatalytic HER of NMZ-S10 could evolve hydrogen at a rate of 4000 μmol g−1 h−1. 30 ppm azobenzene-to-aniline conversion was completely done in 2 h of reaction. Detoxification of 30 ppm hexavalent chromium was conducted in 70 min of reaction. Finally, 10.5 ppm MB–RhB–MO mixed dye degradation was carried out in 1 h of reaction. The as-synthesized NMZ-S10 catalyst has demonstrated its capability to overcome energy and environmental issues promisingly. The great photocatalytic activities are discussed and elucidated with a plausible mechanism to rationalize the superb catalytic performance.
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高影响因子
DYES AND PIGMENTS
·
2020
·
IF 4.613
Huici Shan,Anjie Liu,Yan Lv,Xueyan Wu,Yongdong Ma,Xiaoping Jin,Jixi Guo
Four D−π−A dyads based on various imidazole derivatives donor and o -carborane acceptor moiety have been designed and synthesized for efficient tunable solid-state fluorescence and low-temperature phosphorescence. The results showed that four dyads are all AIEgens with dual emission properties in solution, highly solid-state emission, and low-temperature phosphorescence. The dual emissions were attributed to the locally excited (LE) and twisted intramolecular charge transfer (TICT) emission. The crystallographic measurements and theoretical calculations demonstrated that the strong phosphorescence with a long lifetime up to 2.18 s at low temperature may be attributed to the C–H⋅⋅⋅N, C–H⋅⋅⋅π interactions, strong TICT effect and the reduced vibration coupling by attaching a bulky carborane moiety to the chromophore .
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高影响因子
MICROCHIMICA ACTA
·
2021
·Vol. 188
·期 9
·1-9
·
IF 5.833
Ma Zerui,Li Pan,Jiao Meng,Shi Yu-e,Zhai Yongqing,Wang Zhenguang
Butyrylcholinesterase (BChE) can modulate the expression level of cholinesterase, which emerges as an important clinical diagnose index. However, the currently reported assays for BChE are suffering from the problem of interferences. A ratiometric fluorescence assay was developed based on the MnO 2 nanosheet (NS)–modulated fluorescence of sulfur quantum dots (S-dots) and o -phenylenediamine (OPD). MnO 2 NS can not only quench the fluorescence of blue emissive S-dots, but also enhance the yellow emissive OPD by catalyzing its oxidation reactions. Upon introducing BChE and substrate into the system, their hydrolysate can reduce MnO 2 into Mn 2+ , leading to the fluorescence recovery of S-dots and failure of OPD oxidation. BChE activity can be quantitatively detected by recording the change of fluorescence signals in the blue and yellow regions. A linear relationship is observed between the ratio of F 435 / F 560 and the concentration of BChE in the range 30 to 500 U/L, and a limit of detection of 17.8 U/L has been calculated. The ratiometric fluorescence assay shows an excellent selectivity to acetylcholinesterase and tolerance to various other species. The method developed provides good detection performances in human serum medium and for screening of inhibitors. Graphical abstract
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PubMed
高影响因子
Catalysts
·
2022
·Vol. 13
·期 1
·40
·
IF 4.501
Qiuyun Zhang,Mengmeng Hu,Jialu Wang,Yanting Lei,Yaping Wu,Qing Liu,Yongting Zhao,Yutao Zhang
In this study, the bimetallic Ni-Zr MOF-derived nickel-zirconium oxide (Ni-Zr-O)-impregnated silicotungstic acid (HSiW) nanocomposite catalyst (HSiW@Ni-Zr-O) was prepared via a hydrothermal procedure followed by a pyrolysis treatment, and its structural, morphological, and surface components and oxidation states were characterized by using XRD, FTIR, TPD-NH3, SEM, TEM, N2physisorption, and XPS analyses. Then, the nanocomposite catalysts were successfully applied to the esterification of oleic acid (OA) with methanol. According to its characteristics, the obtained HSiW@Ni-Zr-O-1 catalyst would generate larger pores, a higher acidity, and active interfaces at the calcining temperature of 300 °C. Therefore, HSiW@Ni-Zr-O-1 exhibits an excellent catalytic activity of 95.2% under optimal reaction conditions. Additionally, the catalyst can be reused with a good catalytic activity after nine cycles. This study highlights the opportunity of using bimetallic MOFs as precursors to the synthesis of highly nanoporous metal oxide, which supports the larger-industrial scale production of biofuels.Keywords:silicotungstic acid;MOF;nickel-zirconium oxide;esterification;biofuels;catalysis
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高影响因子
Journal of Inorganic and Organometallic Polymers and Materials
·
2014
·Vol. 25
·期 3
·535-543
·
IF 1.077
Zhou Yong-Hong
Three new multi-dimensional coordination polymers, namely, [Cd(SIP)(HBPP)(BPP) 0.5 (H 2 O)·H 2 O] n ( 1 ), [Zn(L)(BIB) 0.5 ] n ( 2 ), and {[Cd 2 (L) 2 (BIB) 2 ](H 2 O) 7 } n ( 3 ) (H 3 SIP = 5-sulfo-1,3-benzenedicarboxylate, BPP = 1,3-bis(4-pyridyl)propane, H 2 L = 4-oxyacetate-benzoic acid, and BIB = 1,4-bis(imidazol-1-yl)-butane), were hydrothermally synthesized by self-assembly of the flexible N-donor ligand and the polycarboxylate ligands. Single crystal X-ray analyses reveal that complexes 1 – 3 possess different structural features. The Cd(II) atom in complex 1 is seven-coordinated by two bidentate chelating carboxylate groups and two nitrogen atoms as well as one water molecule. The adjacent Cd(II) atoms are bridged by two carboxylate groups to form 1D chains running along different directions, which are connected by BPP ligands to generate 2D network. The resulting 2D networks are further linked by hydrogen-bond interactions, affording a 3D supramolecular architecture. In complex 2 , the [Zn 2 (COO) 4 ] units are bridged by L 2− ligands to generate 1D double chain structure and then linked by BIB ligands to give 2D grid framework. In complex 3 , the [Cd(L 2 )] n and [Cd(BIB)] n helixes are alternately arranged, leading to the formation of a 2D bilayer structure.
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高影响因子
BMC Chemistry
·
2019
·Vol. 13
·期 1
·1-15
·
IF 0
Guo J.,Ma Yu L.,Yu Jia Y.,Gao Yu J.,Ma Ning X.,Wu Xiao Y.
Herein, 2-(2-methoxyphenoxy)-1-phenylethanol (β- O -4), 2-methoxyphenyl anisole (α- O -4) and 4-phenoxyphenol (4- O -5) were selected as typical lignin model compounds. Given the effectiveness of traditional acid–base catalysts for lignin depolymerisation, a novel Ni/CaO–H-ZSM-5(60) catalyst was prepared to investigate the difficulty level of C–O bond of three model compounds cleavage in ethanol. It was observed that Ni/CaO–H-ZSM-5(60) had prominent performance on the C–O bond cleavage at very mild conditions (140 °C, 1 MPa H 2 ). Among them, the C–O bond of α- O -4 and β- O -4 could be completely cleaved within 60 min. Although the C–O bond of 4- O -5 had high bond energy, 41.2% of conversion was occurred in 60 min. The introduction of CaO could regulate the acidity of H-ZSM-5 to enhance the ability to break C–O bonds. Moreover, the possible pathways of C–O ether bonds in three lignin model compounds cleavage were proposed in order to selectively obtain target products from the raw lignin degradation.
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RSC Advances
·
2016
·Vol. 6
·期 47
·41420-41427
·
IF 3.289
Guohui Li,Avinav G. Nandgaonkar,Keyu Lu,Wendy E. Krause,Lucian A. Lucia,Qufu Wei
The engineering of supports for enzyme immobilization while retaining competent functionality is nontrivial. We attempted to enhance the removal efficiency of organics by adopting a relatively novel approach involving a synergy from the adsorption capabilities of a support incorporated with organically modified montmorillonite (O-MMT) and catalytic properties of immobilized laccase. Electrospun polyacrylonitrile (PAN)/O-MMT membranes after alkaline hydrolysis and carboxyl activation were chosen as the support system for laccase immobilization. A confocal laser scanning microscope confirmed a uniform enzyme distribution along with the fibers' longitudinal surface. After enzyme immobilization, the optimum pH shifted from 3 to 3.5, while the optimum temperature remain unchanged at 50 °C. Its stability was preserved despite a large fluctuation in pH (50% of its initial activity retained over the pH range 2–6) and temperature (more than 80% of its initial activity retained over 30–70 °C). Compared to free laccase, the thermal stability of the immobilized laccase was improved after being under 30 °C and 50 °C for 8 h. The operational stability was 68% of the initial one after 10 times repeated usage, while also demonstrating 80% storage stability of the initial activity even after two months. The immobilized laccase showed a high removal efficiency of crystal violet at an optimum pH of 5 and temperature ∼40 °C as well as an initial substrate concentration of 100 mg L−1. Compared with that of the individual support and the free laccase, the removal efficiency by an immobilized enzyme is far higher to confirm a synergy in the immobilized enzyme and support system.
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高影响因子
GREEN CHEMISTRY
·
2015
·Vol. 17
·期 5
·3010-3017
·
IF 8.02
Yao-Bing Huang,Long Yan,Meng-Yuan Chen,Qing-Xiang Guo,Yao Fu
Direct hydrogenolysis of the aromatic Csp2–O bonds in both phenols and phenyl ethers to form arenes selectively is a core enabling technology that can expand greatly the scope of chemical manufacture from biomass. However, conventional hydrogenolysis of phenols typically led to aromatic ring saturation instead of the cleavage of the Csp2–O bonds. Herein, we report a recyclable Ru–WOx bifunctional catalyst that showed high catalytic activities for the hydrogenolysis of a wide range of phenols and phenyl ethers, including dimeric lignin model compounds and the primitive phenols separated from pyrolysis lignin, to form arenes selectively in water. Preliminary mechanistic studies supported that the reactions occurred via a direct cleavage of the Csp2–O bonds and the concerted effects of the hydrogenating Ru sites and the Lewis acidic W sites are the key to such an unusual reactivity.
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高影响因子
FOOD CHEMISTRY
·
2025
·
IF 9.8
Chanchan Sun,Xv Qin,Miaomiao Huang,Xiaoru Wang,Bin Liang,Xiulian Li
The impact of interfacial structure on lipid digestion of emulsions remains controversial, presenting a key limitation in developing technologies for precise regulation of nutritional characteristics through rational food structure design. This study employed pea protein isolate (PPI) microgel particle (PPM) and PPI-κ-carrageenan (κ-CG) composite microgel particle (PPCM) as a model system. The mixing ratio of these macromolecules was adjusted, which changed the interaction of protein and polysaccharide molecules, as well as the interfacial structure of PPCM. Subsequent analysis of structural changes and emulsion digestion in an in vitro simulated digestion model elucidated the regulatory mechanism of interfacial structure on lipid digestion of Pickering emulsions (PPM-E and PPCM-E). The results demonstrated that free sulfhydryl and hydrophobic groups embedded in PPI became exposed during the heat-shearing process of microgel preparation, facilitating disulfide bond formation. The κ-CG gel associated with PPI gel through non-covalent bonds, effectively shielding the exposed hydrophobic groups of PPI. Based on the thickness of the interface, the amount of adsorbed protein, and the protein concentration at the interface, and the surface dilatational modulus, it was found that the deformability of microgel particles at the interface varies. This variation leads to differences in the interfacial structure: PPM formed thick but sparsely distributed interfacial layers due to its limited interfacial deformability; PPCM1 and PPCM2 formed thinner and denser interfacial layers with exposed κ-CG gels on the surface owing to because of their greater deformability compared to PPM; PPCM3, PPCM4, and PPCM5 exhibited the thinnest and densest interfacial layers among the microgel particles, with the exposed κ-CG interconnected to form a polysaccharide network surrounding the oil droplets. Compared with PPM-E, the κ-CG outside the interfacial layer of PPCM1-E and PPCM2-E promoted the expansion of the interfacial microgel in the simulated intestinal fluid and enhanced the hydrolysis by trypsin and lipase, resulting in higher free fatty acid (FFA) release than PPM. In contrast, the κ-CG network outside the interfacial layer of PPCM3-E, PPCM4-E, and PPCM5-E impeded the trypsin and lipase activity, thereby inhibiting the lipid digestion and resulting in lower FFA release than PPM.
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PubMed
高影响因子
Journal of Materials Chemistry C
·
2025
·
IF 5.1
Rui Ding,Wenjuan Zhang,Shiva Pandeya,Xueqing Zhu,Kai Xu,Meixing Gui,Hongbing Wang,Ziliang Li,Qianqian Shang,Mahesh Kumar Joshi
The design of a double Z-type heterojunction represents a promising strategy in photocatalysis to achieve superior charge carrier separation, increased light-harvesting capability, and consequently, a higher photocatalytic reaction rate. Herein, a novel ternary heterojunction with direct dual Z-scheme configuration, g-C3N4/In2S3/In2O3 photocatalyst, was synthesized using a chemical bath and facile calcination process. The XRD, SEM-EDS and XPS results confirmed the successful integration of g-C3N4, In2S3, and In2O3 with preserved crystalline phases. Photocatalytic performances of the ternary composite were evaluated via two effective routes, such as methyl orange (MO) degradation and hydrogen (H2) generation, benchmarked against the pristine g-C3N4 and the g-C3N4/In2S3 and In2S3/In2O3 binary composite, revealing that the in-situ growth of In2O3 onto the g-C3N4/In2S3 composite contributed to the remarkable enhancement of their photocatalytic activity. The photodegradation process follows the pseudo-first order reaction kinetics. The ternary g-C3N4/In2O3/In2S3 heterojunction exhibited 94.8% degradation efficiency of MO with a corresponding rate of 23.4×10-3 min-1, 4.8 times higher than the pristine g-C3N4, and excellent photocatalytic activity in five consecutive cycles. Similarly, the g-C3N4/In2S3/In2O3 heterojunction exhibited a rate constant of ~2.4 mmol h−1 g−1 for H2 generation. This superior enhancement was attributed to the dual Z-scheme charge transfer mechanism. The formation of direct dual Z-scheme heterojunction improved the light harvesting, minimized electron hole recombination, and efficiently facilitated the separation of charge carriers. This work provided a mechanistic insight for engineering multifunctional heterojunction for environmental remediation and pollutant mitigation.
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