JOURNAL OF SOLID STATE CHEMISTRY
·
2022
·
IF 3.656
Liang Qin,Yan Li,Deyun Ma,Fenglan Liang,Lidian Chen,Chenyang Xie,Jiayong Lin,Yani Pan,Guizhen Li,Fenrou Chen,Peiru Xu,Canlin Hong,Jiaxing Zhu
Two transition metal-based MOFs , {[Ni 2 (pip) 2 (bimb) 1.5 ]·2(H 2 O)} n ( 1 ), and {[Zn(pip)(bimb)]·DMF} n ( 2 ) (pip = 5-phenyl-isophthalate, bimb = 1,4-bis(imidazole-1-ylmethyl)benzene) have been successfully prepared. Complex 1 displays a three-dimensional structure with a 7-connected svk topology with a point symbol of (3 3 ∙4 14 ∙5 3 ∙6). Complex 2 performs a two-dimensional (4,4) sql net with channels of 7.0 × 5.5 Å 2 and 10.5 × 4.7 Å 2 along the b and c axis, respectively. The magnetic result of 1 shows an antiferromagnetic coupling between the two metal centers. Desolvated 2 adsorbs around 15.25 wt% 5-fluorouracil (5-FU). The 5-FU was slowly released without any burst release. The degradation of methyl orange caused by oxidizing sulfate radicals (SO 4− ) in a Fenton-like process has also been explored.
研究领域:
无机化学
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材料科学
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药物递送
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环境催化
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配位化学
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DOI
高影响因子
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
·
2018
·Vol. 20
·期 44
·28068-28074
·
IF 3.906
Yue Yu,Sushu Wan,Daocheng Hong,Yuxi Tian
Post-fabrication defect passivation of organometal halide perovskites has become an efficient way to improve their photophysical properties, but the underlying mechanisms are still in debate. In this work, we used p-benzoquinone (p-BQ) to generate surface defects on methylammonium lead triiodide perovskite (MAPbI3), and found that a Usanovich acid–base (O2, acetone or acetonitrile) treatment can effectively passivate those defects and lead to photoluminescence (PL) enhancement. The passivation effect arose from partial neutralization of defect charges via electron transfer between passivation reagents and relevant defects. O2 accepted photo-generated electrons, formed negatively charged oxygen species and attached to the I vacancy site to reduce its PL quenching efficiency by neutralising the defects positive charge. Likewise, acetone accepted photo-generated holes, formed positively charged species and partially neutralised the defects negative charge. The reduced trapping ability of defects caused PL enhancement. In addition, the observed photo-catalysed oxidation of acetone by O2 on the crystal surface supported the single electron transfer mechanism, and showed the potential of MAPbI3 as a photo-catalyst.
研究领域:
材料科学
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光物理学
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半导体材料
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表面化学
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光电功能材料
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DOI
高影响因子
ADVANCED POWDER TECHNOLOGY
·
2022
·Vol. 33
·期 11
·103807
·
IF 4.969
Jingxi Zhang,Yifan Niu,Yu Zhou,Shaohua Ju,Yongwan Gu
In this study, green tea was used as a reducing agent to prepare GT-nZVI/Cu nano-zero-valent iron-copper bimetallic materials for nitrate degradation. Through single factor experiments, the process conditions for nitrate removal by GT-nZVI/Cu were optimized. By measuring the contents of nitrate, nitrite, and ammonia nitrogen in the reaction products, the reduction pathway of nitrate-nitrogen in GT-nZVI/Cu was studied. In addition, the removal mechanism of nitrate by GT-nZVI/Cu was also analyzed by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and kinetic experiments. The results showed that the size of GT-nZVI/Cu particles is between 50 and 70 nm, and they are irregular spherical shapes. The polyphenol antioxidants in green tea make GT-nZVI/Cu have stronger antioxidant properties, and the denitration products are mostly nitrogen. The addition of copper ions accelerates the reaction time and reaction rate. The maximum removal rate of nitrate by GT-nZVI/Cu within 75 min can be up to 99 %. After three repeated experiments, the removal rate of GT-nZVI/Cu can still reach 70 %. The removal mechanism of GT-nZVI/Cu has enhanced nitrate removal through complexation, redox, and adsorption co-precipitation. This study provides a new route for the green preparation and efficient application of nZVI.
研究领域:
环境化学
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纳米材料科学
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水处理技术
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环境功能材料
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污染控制化学
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应用催化
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DOI
高影响因子
JOURNAL OF CATALYSIS
·
2018
·
IF 6.759
Xiaolong Liu,Qingzhen Han,Wenbo Shi,Cheng Zhang,Erwei Li,Tingyu Zhu
In this work, ruthenium-based bimetallic catalysts of 1Ru-5 M/TiO 2 (M = Co, Ce, Fe, Mn, Cu, Ni) were prepared and evaluated in ethyl acetate oxidation. It was found that 1Ru-5Cu/TiO 2 gave the highest catalytic activity. The influence of CuO content and the preparation method on the catalytic activity was also studied. 1Ru-5Cu/TiO 2 showed great catalytic stability in the on-stream reaction test. The influence of H 2 O on the catalytic activity is presented. The bimetallic catalyst 1Ru-5Cu/TiO 2 showed better catalytic performance than the monometallic catalysts 1Ru/TiO 2 and 5Cu/TiO 2 . XRD, TEM, HAADF-STEM, H 2 -TPR, and XPS characterizations were conducted, and the synergistic effect between Ru and Cu was well presented. In situ FTIR studies were also conducted, and the reaction intermediates were revealed on the catalyst surface. The theoretical calculations suggested that ethyl acetate is more easily adsorbed on the CuO surface, while it reacts more easily on the RuO 2 surface . Accordingly, a reaction mechanism for the catalytic oxidation of ethyl acetate over a Ru-Cu bimetallic catalyst is proposed.
研究领域:
催化化学
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环境化学
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表面科学
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材料化学
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物理化学
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DOI
高影响因子
OPTICAL FIBER TECHNOLOGY
·
2013
·Vol. 20
·期 1
·28-31
·
IF 1.187
Jiao-Yang Li,Xu-Guang Huang,Wei Xu,Dong-Rui Xiao,Ze-Bing Zhong
A biocompatible fiber-optic pH sensor based on Fresnel reflection technique and a sensing coating is presented. Sodium alginate and polyethylenimine are alternatively deposited on the sensing fiber end to form the sensing coating via a layer-by-layer electrostatic self-assembly technique. An optical switch is added to the measurement system for the convenience of fast calibration. A linear, monotonic and fast response in a large pH range (from pH 5.87 to pH 10.55) is obtained with the resolution of 0.01 pH unit. The sensitivity of the pH sensor is 0.018 R.I.U/pH. It is not influenced by fluctuations of light source.
研究领域:
生物医学工程
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传感技术
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分子生物学
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转化医学
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生物材料
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DOI
高影响因子
POLYMER
·
2017
·
IF 3.684
Wei Yang,Xu Cheng,Haibo Wang,Yuansen Liu,Zongliang Du
Novel waterborne fluorinated polyurethane (WFPU) based on hydroxyl-terminated poly(fluoroalkyl methacrylates) (HTPFMA) was prepared successfully. The microstructures and micro-phase separation of WFPU were evaluated through infrared spectroscopy (FT-IR), X-ray diffraction (XRD), dynamic mechanical analysis (DMA), and scanning electron microscope (SEM). FT-IR revealed that the H-bonded carbonyl in hard domains increased with the increasing of fluorine content, resulting in enhancing the extent of micro-phase separation between hard and soft segments. XRD results indicated that the crystallinity of hard segment was enhanced with the increasing of fluorine content. The direct visual microstructures by SEM showed that the micro-phase separation was more significant when the fluorine content increased. DMA also revealed strengthened micro-phase separation with increasing fluorine content. The studies of mechanical properties confirmed that WFPU based on HTPFMA had outstanding mechanical properties. The effects of fluorine content on the static contact angles, surface free energy , and surface composition were also studied. The static contact angles of the WFPU films against water and methylene iodide reached around 108° and 84°, respectively. X-ray photoelectron spectroscopy (XPS) confirmed that the fluorine surface enrichment factor in the outermost 10 nm depth was about 10–18 fold higher than its bulk level.
研究领域:
高分子材料科学
·
表面科学
·
材料化学
·
软物质物理
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功能涂层材料
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DOI
高影响因子
Food Analytical Methods
·
2015
·Vol. 9
·期 7
·2026-2035
·
IF 1.956
Du Jiaojiao,Gao Ruixia,Mu Hui
Phthalates represent a potential risk for humans, since they are ubiquitous environmental contaminants. Efficient extraction and purification procedures are demanded for the detection of low concentration levels of phthalates. In this work, a novel type of molecularly imprinted polymers coated onto the surface of vinyl functionalized multi-walled carbon nanotubes was synthesized and coupled with gas chromatography–mass spectrometry (GC/MS) for the selective separation and determination of dioctyl phthalate (DOP) in beverage samples. The morphology, structure property, and thermostability of the resultant polymers were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The adsorption properties of the prepared polymers were investigated by equilibrium rebinding and competitive experiments. The resultant imprinted nanomaterials exhibited high capacity and favorable selectivity. In addition, the feasibility of the developed method using the obtained imprinted polymers as a solid-phase sorbent coupled with GC/MS for the selective isolation and determination of DOP in different beverage samples was demonstrated. Under optimal conditions, the limit of detection of the proposed method for DOP was 2.3 ng L −1 . DOP spiked at three levels of concentration in beverage samples was extracted and determined through the application of the present method, with recoveries ranging from 88.6 to 93.0 % with relative standard deviations less than 5.6 %.
研究领域:
分析化学
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环境毒理学
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食品安全
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分子识别
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材料科学
·
色谱分析
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DOI
高影响因子
POLYMERS FOR ADVANCED TECHNOLOGIES
·
2017
·Vol. 28
·期 11
·1464-1472
·
IF 1.907
Zhankui Mei,Huanhuan Ren,Shaojun Chen,Zaochuan Ge,Jinlian Hu
This study develops a new type of moisture-sensitive shape memory polymer based on zwitterionic copolymers synthesized with acrylic acid (AA) and 3-Dimethyl (methacryloyloxyethyl) ammonium propane sulfonate (DMAPS). The moisture absorption properties of zwitterionic copolymers are particularly investigated in this paper. The results demonstrate that the DMAPS/AA copolymers possess a sulfobetaine structure and form a two-phase separation structure. The zwitterionic copolymers show both good hydrophilic properties and moisture absorption properties. Both AA and DMAPS segments influence the hydrophilic properties and moisture absorption of the composite copolymer. The moisture absorption process is well modeled by Fick's second law in its initial stage. The moisture absorption is mainly determined by immersion conditions and the given materials' structure. Moisture absorption speed and saturated moisture absorption both increase with an increase in DMAPS content as well as the immersion temperature. The increased moisture absorption rate and higher saturated moisture absorption results from the higher activation energy of diffusion. The DMAPS/AA copolymers demonstrate adequate moisture-sensitive shape memory effects. Stain recovery is faster in the zwitterionic copolymers containing higher DMAPS content, whereas the final shape recovery decreases with an increase of DMAPS content. Finally, it is proposed that not only good moisture absorption units are required but also physical crosslinks should be improved for moisture-sensitive shape memory polymers. Copyright © 2017 John Wiley & Sons, Ltd.
研究领域:
高分子材料科学
·
功能高分子
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智能响应材料
·
生物医用材料
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软物质物理
·
环境响应材料
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DOI
高影响因子
Nanoscale
·
2018
·Vol. 11
·期 3
·962-967
·
IF 7.233
Zhaohong Su,Xiaolin Xu,Yongbing Cheng,Yueming Tan,Langtao Xiao,Daili Tang,Hongmei Jiang,Xiaoli Qin,Huixian Wang
A porous graphene (PG) bionanocomposite of PG, gold nanoparticles (AuNPs) and anti-indole-3-acetic acid (anti-IAA) antibody for sensitive and label-free amperometric immunoassay of IAA was reported. A PG film was produced by a pre-reduction/electrochemical reduction process on a glassy carbon electrode (GCE) and then a homogeneous AuNPs layer electrodeposition on the PG film. The anti-IAA antibody was immobilized onto the AuNPs through electrostatic adsorption and covalent conjugation. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy, energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), cyclic voltammetry (CV), elecro-chemical impedance spectroscopy (EIS), ultraviolet visible spectroscopy (UV-vis) and differential pulse voltammetry (DPV) were used to characterize the PG film and the stepwise modification of the immunosensor. The electrochemical immunosensor exhibited a wide linear range from 2 × 10−11 to 2 × 10−8 g mL−1 with a detection limit of 0.016 ng mL−1 (S/N = 3) and showed significant linearity R2 = 0.9970. In addition, the proposed immunosensor showed acceptable selectivity and has been applied to the determination of IAA in the extract samples of several plant seeds with acceptable relative derivation (%) ranging from −5.25% to 4.24% between the immunosensor and high performance liquid chromatography. The proposed chemical pre-reduction and electro-reduction guided protocol can be extended to the preparation of many other functionalized PG nanocomposite films for wide applications.
研究领域:
生物传感
·
纳米生物技术
·
分析化学
·
植物生理学
·
电化学
·
免疫分析
✓ 已验证
DOI
高影响因子
DESALINATION
·
2023
·
IF 9.9
Xudong Bu,Yurong Zhang,Haiqing Guo,Sheng Wang,Xueyan Du
The ion removal capacity of carbon based capacitive deionization (CDI) is limited by the double-layer mechanism. Replacing one electrode of the conventional carbon-based symmetric CDI with a battery-like ion insertion material to obtain hybrid capacitive deionization (HCDI) can significantly improve the adsorption capacity . Various ion insertion materials have been adopted for HCDI, however, how to optimize the performance of the HCDI system by matching the two electrodes with different ions removal mechanism remains challenging. In this work, a HCDI desalination cell was demonstrated by using NaTi 2 (PO 4 ) 3 /reduced graphene oxide composites (NTP-rGO-700) as the cathode and activated carbon (AC) as the anode. Based on the mass balance strategy of electrodes and the electrochemical behavior of hybrid capacitors with different AC:NTP-rGO-700 mass ratios, the HCDI desalination cell was assembled with the optimal AC:NTP-rGO-700 mass ratio of 2:1. At an operating voltage of 1.6 V and a current density of 125 mA·g −1 , the specific adsorption capacity (SAC) of the HCDI cell can reach 51 mg·g −1 with an average salt adsorption rate (ASAR) of 2 mg·g −1 ·min −1 , and the energy consumption (E m ) is 136.53 kJ·mol −1 . This work provides an efficient approach for developing high performance HCDI cell.
研究领域:
环境科学
·
电化学
·
材料科学
·
水处理技术
·
能源存储
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DOI
高影响因子
ELECTROCHIMICA ACTA
·
2015
·
IF 4.504
Peng Li,Lianyi Shao,Pengfei Wang,Xi Zheng,Haoxiang Yu,Shangshu Qian,Miao Shui,Nengbing Long,Jie Shu
In this work, Li 2 NaV 2 (PO 4 ) 3 is successfully synthesized by using a simple solid-state reaction method. Structural analysis shows that this sample is a hybrid product consisted of rhombohedral Li 3 V 2 (PO 4 ) 3 phase and rhombohedral Na 3 V 2 (PO 4 ) 3 phase As a cathode material for lithium ion batteries, Li 2 NaV 2 (PO 4 ) 3 exhibits an initial reversible capacity of 108.9 mAh g −1 at 35 mA g −1 in the potential range between 3.0 and 4.3 V, with an average working potential at 3.75 V. The lithium-ion diffusion coefficient in Li 2 NaV 2 (PO 4 ) 3 is measured to be 1.86–3.27 × 10 −15 cm 2 s −1 . In addition, the electrochemical reaction between Li 2 NaV 2 (PO 4 ) 3 and Li is also investigated by various in-situ and ex-situ techniques. Viewed from the in-situ and ex-situ results, it is concluded that the electrochemical reactions of Li 2 NaV 2 (PO 4 ) 3 with Li are associated with the formation of rhombohedral LiV 2 (PO 4 ) 3 phase and rhombohedral NaV 2 (PO 4 ) 3 phase during the lithium ion extraction process and its reverse lithium insertion process is reversible for structural evolution. The highly stable structure ensures the electrochemical reversibility of Li 2 NaV 2 (PO 4 ) 3 cathode material in lithium ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
固体化学
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DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2017
·Vol. 42
·期 34
·22294-22301
·
IF 3.582
Jiang Li,Tianmu Lv,Nianjun Hou,Ping Li,Xueli Yao,Lijun Fan,Tian Gan,Yicheng Zhao,Yongdan Li
The effects of Mo doping into the B-site of La 0.3 Sr 0.7 TiO 3-δ perovskite on its ionic conductivity and catalytic activity as an anode material of solid oxide fuel cells have been investigated. The partial substitution of Ti by Mo reduces the bond energy between metal and oxygen ions in the perovskite. The concentration of Mo 5+ /Mo 6+ redox couples increases with the rise of the content of Mo, while the oxygen ionic conductivity decreases simultaneously. The doping of Mo significantly reduces the anodic polarization resistance and improves the performance of the single cell. The cell with La 0.3 Sr 0.7 Ti 0.97 Mo 0.03 O 3-δ anode and La 0.8 Sr 0.2 Ga 0.8 Mg 0.2 O 3-δ electrolyte exhibits a maximum power density of 135 mW cm −2 at 850 °C with hydrogen as fuel.
研究领域:
材料科学
·
电化学
·
能源材料
·
固态离子学
·
燃料电池技术
✓ 已验证
DOI
高影响因子