NANO
·
2019
·
IF 1.293
Yanwei Sui,Man Zhang,Haihua Hu,Yuanming Zhang,Jiqiu Qi,Fuxiang Wei,Qingkun Meng,Yezeng He,Yaojian Ren,Zhi Sun
The interconnected three-dimensional Ni–Co–S nanosheets were successfully deposited on ZnO nanorods by a one-step potentiostatic electrodeposition. The Ni–Co–S nanosheets provide a large electrode/electrolyte interfacial area which has adequate electroactive sites for redox reactions. Electrochemical characterization of the ZnO@Ni–Co–S core–shell nanorods presents high specifc capacitance (1302.5 F/g and 1085 F/g at a current density of 1 A/g and 20 A/g), excellent rate capabilities (83.3% retention at 20 A/g) and great cycling stability (65% retention after 5000 cycles at a current density of 30 A/g). The outstanding electrochemical performance of the as-prepared electrode material also can be ascribed to these reasons that the special structure improved electrical conductivity and allowed the fast diffusion of electrolyte ions.
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高影响因子
CHEMICAL RESEARCH IN CHINESE UNIVERSITIES
·
2019
·Vol. 35
·期 5
·937-944
·
IF 1.071
Liu Zhenchao,Wang Peng,Hu Wei,Liu Baijun
A series of novel organic-inorganic hybrid proton-conducting electrolyte membranes with silane-crosslinked sulfonated poly(aryl ether ketone)(SC-SPAEK) networks was prepared via a simple procedure that includes solution casting and acid treatment. The organosilicon pendants of the silane-grafted SPAEK, which were expected to serve as coupling and crosslinking agents, were found to play a key role in the homogenous dispersion of inorganic particles and improved the performance of hybrid membranes. The hybrid membranes exhibited enhanced proton conductivity, and SC-SPAEK/TiO 2 -4 showed an extremely high proton conductivity of 0.1472 S/cm at 100 °C. The crosslinked hybrid membranes also demonstrated good chemical resistance, oxidative stability, and mechanical properties. The crosslinked hybrid membranes with excellent comprehensive performance may be a promising material for proton exchange membrane fuel cells.
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APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
·
2019
·Vol. 103
·期 20
·8351-8361
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IF 3.67
Liu Xiaofeng,Xia Yongjun,Zhang Yao,Yi Zhenwei,Meng Peng,Wang Guangqiang,Ai Lianzhong
This study describes the application of in situ extractive fermentation (ISEF) to increase the yields of antroquinonol (AQ) and antrodin C (AC) from Antrodia camphorata S-29. In initial screening experiments, nine solvents were tested to identify the most suitable extractant for the in situ extraction of AQ and AC. These solvents included n-tetradecane, n-dodecane, n-decane, heavy paraffin, light paraffin, oleyl alcohol, oleic acid, butyl oleate, and isopropyl myristate. Of these, oleic acid was the most suitable solvent for the in situ extraction of AQ and AC. The use of oleic acid as an in situ extractant significantly improved AQ and AC productions, which were approximately 5-fold and 8-fold that of the control, respectively. The recovered oleic acid was treated with a silica gel solid-phase extraction column, which was able to rapidly adsorb the bioactive metabolites. The separated solvent hardly contained fermentation products and could be directly reused in ISEF. AQ and AC were obtained with purities of over 75% by silica gel column chromatography. The recoveries of AQ and AC reached 70.7 ± 0.8% and 81.5 ± 1.2%, respectively.
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PubMed
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2019
·
IF 4.084
Bin Shen,Hongting Pu
Anion exchange membranes with high ionic conductivity and dimensional stability attract a lot of research interests. In present study, a series of fluorene-containing poly(arylene ether sulfone)s containing imidazolium on the flexible long side-chain are synthesized via copolycondensation, Friedel-Crafts reaction, ketone reduction, and Menshutkin reaction sequentially. The membranes used for characterization and membrane electrode assembly are obtained by solution casting and ion exchange thereafter. The morphology of the membranes is studied via transmission electron microscopy , and the microphase separation is observed. The long side-chain structure is responsible for the distinct hydrophilic-hydrophobic microphase separation, which facilitates the transport of hydroxide ions in the membranes. The incorporation of imidazolium on the flexible long side-chain is favorable for the ionic aggregation and transport in the membranes. The resulted membranes exhibit high hydroxide conductivities in the range of 48.5–83.1 mS cm −1 at 80 °C. All these membranes show good dimensional stability and thermal stability. The single cell performance shows a power density of 102.3 mW cm −2 at 60 °C using membrane electrode assembly based-on one of the synthesized polymers.
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ELECTROCHIMICA ACTA
·
2018
·
IF 5.116
Yuebin Yang,Hui Xu,Shanxing Wang,Yuanfu Deng,Xianying Qin,Xusong Qin,Guohua Chen
Li-ion batteries have held a dominant position in the energy storage area for decades. However, due to the limitation of its chemistry , the energy density of Li-ion batteries is limited to ∼300 W h kg −1 . In recent years, more attention has been paid to the Li-S batteries that are environmentally friendly, cost-effective and high energy density (theoretical value of cathode: ∼2600 W h kg −1 ). In this study, carbonized polydopamine (C-PDA)-coated hollow carbon nanofibers (CNFs) with TiO 2 nanoparticles interspersed in the void space between the CNF skeleton and carbon coating layer were subtly designed. The C-PDA/TiO 2 /CNF composite (CTC) was integrated with the commercial separator as a polysulfide filter to achieve high-performance Li-S batteries. It is reveals that the CTC coating layer could effectively filter and reactivate the dissolved polysulfides to achieve a stabilized sulfur-based cathode. The Li-S battery assembled by this integrated separator and the regular cathode (sulfur/Ketjen black) with 72.7 wt% of sulfur achieved a high specific capacity and low decay rate (632.5 mAh g −1 at the first cycle and 0.06% per cycle) at 2.0C for 500 cycles. These good results indicate that the C-PDA/TiO 2 /CNF-modified separator could be a promising separator candidate for high performance Li-S batteries.
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高影响因子
JOURNAL OF MATERIALS RESEARCH
·
2019
·Vol. 34
·期 14
·2445-2455
·
IF 1.982
Uwamahoro Evariste,Guohua Jiang,Bo Yu,Yongkun Liu,Zheng Huang,Qiuling Lu,Pianpian Ma
In this work, hierarchical mesoporous Zn–Ni–Co–S–rGO/NF microspheres have been prepared by hydrothermal, sulfurization, and subsequent calcination process. The effect of different sulfurization time on the morphology and capacitance of composites was tested. The high electrochemical performance of (Zn–Ni–Co–S–rGO/NF) composite was obtained when the sulfurization time was 3 h (Zn–Ni–Co–S–rGO/NF-3h), where a specific capacitance of 627.7 F/g at 0.25 A/g and excellent rate capability of about 97.8% capacitance retention at 2 A/g after 4000 cycles were achieved. Moreover, an asymmetric supercapacitor fabricated by (Zn–Ni–Co–S–rGO/NF-3h) composite and activated carbon (AC) as the positive and the negative electrodes, respectively, showed a high energy density of 75.96 W h/kg at a power density of 362.49 W/kg with a remarkable cycle stability performance of 91.2% capacitance retention over 5000 cycles. This incredible electrochemical behavior illustrates that the hierarchical mesoporous Zn–Ni–Co–S–rGO/N-3h microsphere electrodes are promising electrode materials for application in high-performance supercapacitors.
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高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2019
·
IF 7.015
Xiaocui Han,Yunji Xie,Di Liu,Zheng Chen,Haibo Zhang,Jinhui Pang,Zhenhua Jiang
The advancement of proton conductive applications will require the identification of new membrane with high-conductivity and good dimensional stability that can be readily obtained and cheap. We reported a novel rigid carbazole derivative and proton exchange membrane consisting of densely sulfonated carbazole derivative, which could form aggregated ionic cluster of sulfonic acid group and result in continuous broad-dimensional nanochannels. The SAXS analysis confirmed these copolymers owned large ion clusters. All of membranes prepared in this work were thermally stable at up to 250 o C. These membranes also exhibited excellent dimensional stability and outstanding proton conductivity. SPESK-Cz-15 with IEC = 2.07 meq g -1 showed the largest water uptake with a value of 107%, but the swelling ratio was only 36.4% at 100 o C, which was attributed to the artful structure of the copolymers. SPESK-Cz-15 showed very high proton conductivity (165.3 mS cm -1 at 80 o C), which was 1.53 times higher than that of Nafion 117 (108 mS cm -1 at 80 o C). Besides, the maximum power density of SPESK-Cz-15 was 1642.7 mV cm -2 at 80 o C under 95% RH. The stability of single cell based on SPESK-Cz-15 was remarkable. All above indicate that SPESK-Cz-x are potential materials for polymer electrolyte membrane fuel cells in the future.
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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
·
2019
·
IF 4.978
Fekadu Tadesse Bekena,Hairus Abdullah,Dong-Hau Kuo,Misganaw Alemu Zeleke
Novel Mg-doped Zn(O,S) nanoparticles were synthesized by a chemical precipitation process at 90 ℃ and the prepared nanoparticles were characterized by XRD, SEM, HRTEM, XPS, UV–vis, DRS, PL, EIS, and photocurrent response. The photocatalytic reduction for the 4-nitrophenol using Na 2 SO 3 under UV light irradiation showed that Mg–Zn(O,S)-2.5 exhibited higher activity compared with other samples. 96.7% of 4-nitrophenolate ion reduced into 4-aminophenol within 45 min. Mg–Zn(O,S)-2.5 was also tested for hydrogen evolution, where the rates of 1035 μmol/g for the 4-NP-free sample and 705 μmol/g for the 4-NP-added one were achieved. Finally, the stability and reaction mechanism was mentioned.
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高影响因子
RSC Advances
·
2019
·Vol. 9
·期 27
·15196-15204
·
IF 3.049
Yun Hong,Dongsen Mao,Rui Wu,Zhe Gao,Tingting Meng,Rongrong Wang,Lin Liu,Jing Miao
DNAzymes have the potential to suppress gene expression through sequence-specific mRNA cleavage and can therefore play an important role in various gene therapies. Hepatitis B virus (HBV) is still one of the most serious liver infections in people around the world and is difficult to treat. We previously designed a 10-23 DNAzyme called DrzBS, which targets HBV S gene expression, but this enzyme depends on exogenous delivery, and so its application has been limited. To overcome this limitation, we have now developed a chitosan-based nanocarrier (chitosan-g-stearic acid, CSO–SA) for intracellular delivery of DrzBS, then compared the inhibition effect of our CSO–SA/DrzBS complex to a common transfection reagent, Lipofectamine™ 2000/DrzBS, on hepatitis B surface antigen expression. The synthesized CSO–SA assembles into micelles in an aqueous solution and exhibits excellent cytoplasmic targeting, and could protect DrzBS from degradation by ribonuclease. CSO–SA/DrzBS showed a higher inhibition rate (IR) than Lipofectamine™ 2000/DrzBS. Moreover, at the same DrzBS concentration (1.2 μmol L−1), the maximum IR of CSO–SA/DrzBS micelles was 2.4-fold that of the Lipofectamine™ 2000/DrzBS complex, and held on for 96 hours. Compared with Lipofectamine™ 2000/DrzBS, CSO–SA/DrzBS achieved a higher HBV inhibition effect. This study demonstrates that CSO–SA micelles can serve as a potential vector for DrzBS and that CSO–SA/DrzBS micelles are a promising application for anti-HBV gene therapy.
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PubMed
高影响因子
JOURNAL OF POLYMER RESEARCH
·
2019
·Vol. 26
·期 7
·1-7
·
IF 1.53
Deng Hongyang,Xu Yewei,Lei Hong,Lei Yonglin,Huo Jichuan,Zhang Lin
3,5-bis(2-benzimidazolyl) pyridine (3,5-BP) is synthesized and a series of benzimidazolyl and pyridyl-containing poly (ether ether ketone) s (mPEEK-BPs) with precise structures and high yield are prepared through a nucleophilic displacement reaction of 3,5-BP, m-dihydroxybenzene and 4,4′-difluorobenzophenone. X-ray diffraction results show that mPEEK-BPs are amorphous. All the synthesized polymers posses high glass transition temperatures ( T g = 211~270 °C) and high thermal stability ( T d5% = 506~549 °C in N 2 , 471~564 °C in air). The polymers have good solubilities in common organic solvents. With the increase of benzimidazole and pyridine units content, the thermal properties and solubility of the as-prepared polymers improved. Additionally, the resulted polymers exhibit excellent fluorescence performance and the fluorescence emission peak appears at 425 nm.
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高影响因子
BIORESOURCE TECHNOLOGY
·
2019
·
IF 6.669
Juanli Liu,Baiqin Zhou,Hong Zhang,Juan Ma,Bin Mu,Wenbo Zhang
A novel wasted sludge-based Biochar modified by Chitosan and Fe/S (BCFe/S) was prepared for tetracycline (TC) removal from water. To investigate the similarities and differences in adsorption behaviors between Biochar and BCFe/S, characterization, kinetics, isotherms and thermodynamics were discussed. The studies on site energy distribution (SED) were also presented. The results showed that the maximum TC adsorption amount was 51.78 mg/g for Biochar, while it was 183.01 mg/g for BCFe/S-4. Meanwhile, electrostatic attraction, π-π stacking, pore filling, silicate bonding and hydrogen bonding were the main adsorption mechanisms for TC removal by Biochar. Besides above mechanisms, chelating and ion exchange were also accounted for adsorption mechanisms for TC uptake by BCFe/S-4. Moreover, SED results revealed that the surface of Biochar was more homogeneous while the surface of BCFe/S-4 was more heterogeneous at higher temperature. Findings of this work could offer valuable information in designing adsorbents and investigating adsorption mechanisms.
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INORGANIC CHEMISTRY
·
2019
·
IF 4.85
Ailijiang Abudurusuli,Kui Wu,Junjie Li,Alimujiang Yalikun,Zhihua Yang,Shilie Pan
A series of metal chalcogenides, LiBa2MIIIQ4 (MIII = Al, Ga, In; Q = S, Se), have been successfully obtained by the sealed-tube method. LiBa2MIIIQ4 undergoes a special structural transformation from the P21/m (LiBa2AlQ4 and LiBa2GaS4) to the P21/n (LiBa2InQ4) space group, which leads to disparities in electronic states, birefringence, and band gaps. Their structures feature the same zigzag [LiMIIIQ4]4– layers consisting of corner-shared LiQ4 and MIIIQ4 tetrahedra. The Ba atoms serve to bridge the [LiMIIIQ4]4– layers. The structural comparisons show that the radii of MIII and the coordination environments of the Ba atoms (BaQ7 vs BaQ8) cooperatively affect the structural transition from simple mirror m to diagonal glide n in LiBa2MIIIQ4. In addition, a statistical analysis uncovers that the MIII/Ba atomic ratio also plays an important role in regulating the structural transition in Ba- and MIII-based chalcogenides.
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