RSC Advances
·
2015
·Vol. 5
·期 113
·93415-93422
·
IF 3.84
Jie Wang,Haibing Wei,Shanzhong Yang,Huagao Fang,Pei Xu,Yunsheng Ding
A series of poly(phenylene oxide)s (PPOs) bearing a flexible pendent imidazolium cation were prepared by an azide–alkyne cycloaddition between azidomethylated PPO and a novel alkyne-containing imidazolium, and their structures were confirmed by 1H NMR, 13C NMR, and FT-IR. The corresponding anion exchange membranes (AEMs) showed distinct hydrophobic/hydrophilic phase-separated morphology at higher imidazolium content, as evidenced by AFM and SAXS techniques, which favors for the construction of interconnected hydroxide transport channels. As a result, the as-prepared AEMs exhibited higher conductivity (95 mS cm−1, 80 °C, 100% RH) than conventional imidazolium benzylic-type AEM (55 mS cm−1, 80 °C, 100% RH) with even lower IEC. Furthermore, the introduction of a 1,2,3-triazole moiety into the polymer side chain does not compromise its thermal and alkaline stability. This investigation demonstrated that the “click chemistry” strategy will benefit further tailoring of high performance AEMs with “side-chain-type” architectures.
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CHINESE JOURNAL OF CHEMISTRY
·
2014
·Vol. 32
·期 8
·771-776
·
IF 1.04
Mo Sun,Hengyi Zhang,Xinyue Hu,Bowen Liu,Yu Liu
A hyperbranched supramolecular polymer (HSP) is constructed based on the intermolecular inclusion complexation of bridged tris(permethyl- β -cyclodextrin) with Mn III -porphyrin bearing poly(ethylene glycol) (PEG) side chains (Mn III -TPP), and characterized by UV/vis absorption spectroscopy, isothermal titration calorimetry (ITC), NMR, dynamic light scattering (DLS), atomic force microscopy (AFM) and transmission electron microscopy (TEM), respectively. The presence of permethyl- β -cyclodextrin can stabilize the low-valent Mn II -TPP. In vitro cell experiment indicates that this HSP has no remarkable cellular toxicity against NIH 3T3 cells. In vitro MR imaging experiment indicates a slightly increased T 1 relaxivity for this HSP compared to that for the linear supramolecular polymer.
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ECS Journal of Solid State Science and Technology
·
2015
·Vol. 5
·期 2
·P21
·
IF 1.558
Bin Hu,Wen Luo,Lin Jin,Zengchen Liu,Mengnan Wang,Liuyang Zhou,Chunyang Li
Two novel carbazole-3, 4-ethoxylenedioxythiophene (EDOT) derivatives containing acceptor groups such as benzonitrile and phthalonitrile were synthesized and characterized. Both the monomers could be electrochemically polymerized and form stable electroactive polymer films. Spectroelectrochemical technique were performed to investigate the electrochemical and optical changes of the resulting polymer films, multi-electrochromic properties upon different applied potentials suggested the effect of the benzonitrile and phthalonitrile units and their potential applications in electrochromic device. Furthermore, scanning electron micrographs (SEM) were used to study the microstructure morphology of polymer films.
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GREEN CHEMISTRY
·
2014
·Vol. 17
·期 2
·1269-1275
·
IF 6.852
Qingwen Tian,Lijian Huang,Wangen Zhao,Yanchun Yang,Gang Wang,Daocheng Pan
Aqueous solution deposition of metal chalcogenide semiconductor thin films is considered a green and low-cost approach. However, it is hard to find a general aqueous solution approach to deposit various kinds of high-quality metal sulfide thin films. Here, we describe a green and robust ammonium thioglycolate aqueous solution approach, and fifteen types of metal sulfide precursor solutions (metal = Cu, Zn, Sn, Ge, In, Sb, Mg, Cd, Mn, Bi, Fe, Ni, Li, Na, K) can be prepared using metal oxides or metal hydroxides as raw materials at room temperature under an air atmosphere. Moreover, elemental sulfur and selenium can also be highly dissolved. By this green route, high quality CZTS nanocrystal thin films can be deposited by directly coating the mixed Cu, Zn, and Sn precursor solutions without the need for complex nanocrystal synthesis. The remarkable power conversion efficiency of 6.62% was achieved, which is the highest value for aqueous solution deposited CZTSSe thin film solar cells.
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JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
·
2013
·
IF 2.823
Jian-Yong Zheng,Jia-Yu Wu,Yin-Jun Zhang,Zhao Wang
The mycelium of Aspergillus oryzae WZ007 was successfully developed to kinetic resolution of ( R , S )-ethyl-2-(4-hydroxyphenoxy) propanoate (( R , S )-EHPP) for production of ( R )-ethyl-2-(4-hydroxyphenoxy) propanoate (( R )-EHPP). The key biocatalytic process parameters (pH, temperature, rotation speed and substrate concentration) were optimized. Under the optimum conditions, the optical purity of ( R )-EHPP was improved up to >99% when the conversion was above 49%. A. oryzae WZ007 whole-cell lipase exhibited high reaction capacity, enantioselectivity and good reusability. The tolerable substrate concentration was 0.5 mol/L, and dry mycelium of A. oryzae WZ007 maintains over 80% of its initial activity after eight repeating cycles. Therefore the enzymatic preparation of ( R )-EHPP route was suitable for industrial application.
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JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
·
2014
·Vol. 119
·期 3
·1913-1921
·
IF 2.206
Wang Hui,Wang Jun,Feng Tian-tian,Ramdani Noureddine,Li Yue,Xu Xiao-dong,Liu Wen-bin
A series of fluorene-based benzoxazine-endcapped copoly(ether ketone ketone)s (co-PEKKs) were successfully synthesized, in which the co-PEKKs were prepared with different molar ratios of 2,7-dihydroxy-9-fluorenone to bisphenol-A. The obtained phenol-ended co-PEKKs reacted with formaldehyde and n -butylamine to yield the benzoxazine-endcapped co-PEKKs (B-PEKKs). The structure of these oligomers was studied by Fourier transform infrared spectroscopy and 1 H nuclear magnetic resonance spectroscopy, and the molecular mass of these phenol-ended co-PEKKs was detected by gel permeation chromatography. The thermal behaviors of these B-PEKKs were determined by differential scanning calorimetry. In addition, the thermal and dynamic mechanical properties of the polymer films were investigated by thermogravimetric analysis and dynamic mechanical analysis. The results indicate that the incorporation of co-PEKKs within the benzoxazine backbone considerably improves the toughness of the fluorene-containing polybenzoxazines without much sacrifice of their thermal properties. Furthermore, as the content of 2,7-dihydroxy-9-fluorenone increases, the T
5 values decrease, while the T
g values and char yields of the prepared polymers increase to reach their highest values at 256 °C and 64 %, respectively.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Xingyu Zhan,Yunxiong Zeng,Bo Hong,Xinqing Wang,Yingchun Xia
Artificial photosynthesis for H 2 O 2 production through O 2 reduction is a sustainable and cost-effective technology for the scientific and industrial communities. Metal-free polymeric carbon nitride (CN) is a promising visible-light responsive semiconductive material for photocatalytic H 2 O 2 production. However, its inherently disordered and amorphous structure limits its performance improvement due to high photogenerated carrier complexation and sluggish interlayer charge transfer. Here, we report a high-performance S-type heterojunction, composed of CeO 2 coupled with N -vacancy-rich CN (CeO 2 /Nv-CN), that enhances the photocatalysis of H 2 O 2 production under visible light. The prepared CeO 2 /Nv-CN showed an H 2 O 2 generation rate of up to 69.79 mmol·g −1 ·h −1 , 48.80-fold higher than CN and had an apparent quantum yield of 13.8 % at 400 nm. A synergistic effect among CeO 2 , N -vacancies (Nv) and S-type heterojunction is responsible for such an excellent activity, which increased the O 2 and light absorption sites, built rapid charge diffusion channels, and enhanced two-electron O 2 reduction. This work demonstrates the potential of incorporating nanosized CeO 2 with CN to achieve high-performance photocatalytic H 2 O 2 production, opening new avenues for designing highly efficient polymeric composite photocatalysts for energy conservation.
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PubMed
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DALTON TRANSACTIONS
·
2024
·Vol. 53
·期 36
·15330-15337
·
IF 3.5
Fangzheng Qi,Zengsheng Guo,Yuhan Zhang,Xue-Na Tang,Yiqiang Sun,Bo Xu,Guang-Ning Liu,Cuncheng Li
The stable contact of heterogeneous interfaces and the substantial exposure of active sites are crucial for enhancing the photocatalytic performance of semiconductor catalysts. However, most reported two-dimensional (2D)/2D CsPbBr3 and BiOCl heterostructures are fabricated using electrostatic self-assembly methods, which exhibit significant deficiencies in precise interface quality control and effective active site exposure. In this study, we fabricate a zero-dimensional (0D)/2D CsPbBr3/BiOCl heterojunction via a two-step calcination method, achieving an efficient direct S-scheme configuration. Optimizing interfacial contact and band alignment between CsPbBr3 quantum dots and BiOCl nanosheets enhances cross-plane charge transfer, promoting superior charge separation. This 0D/2D CsPbBr3/BiOCl heterojunction exhibits enhanced carrier mobility and high conversion rates without cocatalysts or sacrificial agents. The mechanism underlying the accelerated S-scheme charge transfer is comprehensively elucidated through a combination of analytical techniques and density functional theory (DFT) calculations. This study offers a novel approach for managing charge carrier segregation and mobility in CO2 reduction photocatalysts.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Xiaohua Zheng,Mengnan Xu,Chenbin Cai,Yanhaohan Yuan,Feng Lin,Wei Chen,Fanger Yang
Photocatalysis is a green approach to solving energy and environmental problems, and researchers are still pursuing high-performance photocatalysts . Although BiOX (X = Cl or Br) has a suitable bandgap and good stability, its photoresponse is mostly concentrated in the UV region. Conversely, SnS 2 has a wide photoresponse range but exhibits perceptible photocorrosion and poor stability. To exploit the advantages of both BiOX and SnS 2 , this study hydrothermally synthesized and introduced superfine SnS 2 (∼30 nm in size) into a BiOCl/BiOBr binary system to fabricate BiOCl/BiOBr/SnS 2 composites. Subsequently, the degradation performance of these composites in a Rhodamine B solution under visible light was investigated. Results show that the BiOCl/BiOBr/SnS 2 heterojunctions were successfully prepared and the composites exhibited the best photocatalytic performance with 6% mass fraction of SnS 2 (BiOCl-to-BiOBr mol ratio = 1:1). The formation of a double S-schedule heterojunction between BiOCl/BiOBr and SnS 2 not only accelerated charge separation and transfer but also broadened the photoresponse range and reduced photoelectron–hole recombination under full-spectrum irradiation. Loading a small narrow-bandgap photocatalyst onto a large photocatalyst provides an effective way to construct heterojunctions with excellent photocatalytic performance. The ternary photocatalyst presents a favorable photocatalytic stability, and its photodegradation rate is 4.6, 4.5 and 220.5 times that of BiOCl, BiOBr and SnS 2 , respectively.
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npj Science of Food
·
2025
·Vol. 9
·期 1
·1-9
·
IF 7.8
Liu Kai,Lian Yinyin,Xie Xingyun,Gao Yuyang,Song Jiajia,Suo Huayi,Zhang Yu
This study investigates the impact of O. oeni on the quality of blueberry wine, employing various analytical methods to determine parameters such as alcohol content, antioxidant capacity, organic acids, amino acids, and volatile components. The results demonstrated that co-inoculation with O. oeni significantly decreased the titratable acidity of blueberry wine. Among the organic acids, the malic acid content of ST and SE groups decreased by (26.24 ± 1.24)% and (35.75 ± 4.02)%, respectively. The main consumed amino acids were aspartate, lysine, and arginine after co-inoculation with O. oeni . Additionally, co-inoculation with O. oeni significantly increased the content of medium-chain fatty acid ethyl esters, especially isoamyl acetate content. The antioxidant capacity of blueberry wine was significantly enhanced by co-inoculation with O. oeni , particularly in terms of measurement of 1,1-diphenyl-2-picryl-hydrazyl (DPPH) clearance. The findings of this study provide a solid basis for improving the quality of blueberry wine and promoting the growth of blueberry wine industry.
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JOURNAL OF MOLECULAR LIQUIDS
·
2024
·
IF 5.3
Yuchi Liu,Bingxiu Xue,Ruijing Ma,Xiaopeng Zhao,Jianbo Yin
Poly(ionic liquid)s (PILs) are providing potential platforms to develop next generation water-free polyelectrolyte-based electrorheological (ER) fluids because they well overcome water sensitivity problem of classic polyelectrolyte-based ER fluids by incorporating with large size fluoric counterions. Especially, crosslinked PILs (CPILs) can further broaden the working temperature range of ER effect compared to linear PILs. However, the crosslinking network easily restricts the ion dissociation due to decreased dielectric constant and thus weakens ion movement-induced interfacial polarization and ER effect. In this paper, we propose a way to improve ion dissociation and ion movement-induced interfacial polarization of CPILs by doping polar aniline oligomer to improve the dielectric constant of CPILs. Several kinds of CPILs are synthesized and then aniline oligomer is doped into CPILs by swelling method. The structure of doped CPILs is characterized by different techniques, the dielectric property of ER fluids of doped CPIL particles in silicone oil is analyzed by dielectric spectroscopy, and the ER effect of ER fluids of doped CPIL particles is measured by rheometer under electric fields. It shows that doping aniline oligomer can increase the dielectric intensity and decrease the relaxation time and corresponding activation energy of interfacial polarization and improve the ER effect of CPILs with a relatively loose crosslinking network, while doping aniline oligomer has no contribution to the interfacial polarization and ER effect of CPILs with a relatively tight crosslinking network.
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International Journal of Peptide Research and Therapeutics
·
2024
·Vol. 30
·期 5
·1-13
·
IF 2
Liu Ziyang,Wei Yuping,Zhang Man,Zhu Xingyan,Liu Kun
Angiotensin-converting enzyme-2 (ACE2) is a important cell surface receptor of SARS-CoV-2 S protein. The initial stage of SARS-COV-2 cell infection involves the binding of the S protein to ACE2. Hence, this work presents an innovative strategy to designing ACE2-based peptide inhibitors by considering the surface property and morphology of the S protein RBD. The aim is to develop a short peptide inhibitor that can effectively inhibit S protein-ACE2 interaction Through computational analysis and molecular simulation, the surface properties and morphology of S protein receptor-binding structural domain (RBD) were investigated, while the key residues of ACE2 ligand-binding structural domain (LBD) were identified based on their contributions and non-covalent interactions. Then, peptide inhibitors, consisting of ACE2 key residues, were developed by fitting to the surface characteristics and topographical features of the S protein RBD. Molecular simulation showed that two novel short peptides, IEPFF (I5) and WIEPFF (W6) had high affinity for S protein RBD but a low affinity for the cell membrane. Cellular adsorption studies demonstrated that both I5 and W6 effectively blocked ACE2-S protein binding without significant cytotoxicity. Flow cytometry analysis revealed that both I5 and W6 effectively inhibited S protein binding to the ACE2, resulting in a significant reduction (75 and 79%, respectively) in fluorescence intensity after 30 min of incubation at a concentration of 200 μM. Both I5 and W6 were excellent potential anti SARS-COV-2 drugs. This work provides an innovative perspective for the development of functional peptides for the prevention and management of SARS-COV-2.
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