DALTON TRANSACTIONS
·
2020
·Vol. 49
·期 46
·17033-17038
·
IF 4.174
Weichi Liang,Jiali Wen,Yukai Zhao,Meng Zhang,Jiuxing Jiang
A layered aluminophosphate |C14H11NO|2[Al4(HPO4)4F4(H2O)2] (denoted as SYSU-2) with a new topology has been hydrothermally synthesized with N-methyl-9-acridone (NMA) as the organic structure-directing agent. Single-crystal X-ray diffraction analysis reveals that SYSU-2 crystallizes in a triclinic space group P, with the inorganic sheets stacked in an AA sequence. Hydrogen bonds are responsible for the neutral inorganic–organic layer connection. The layer structure of SYSU-2 is constructed by alternating AlO4F2 octahedra and PO4 tetrahedra. The topological analysis of SYSU-2 indicates an independent topology. The NMA layers are self-assembled with π–π interaction. SYSU-2 crystals show interesting dual-band emission fluorescence properties compared with NMA crystals. Under 406 nm UV irradiation, SYSU-2 crystals emit yellow light with two emission bands at 477 and 566 nm, while NMA crystals emit blue light with only one band at 473 nm. The differences may be derived from the difference of stacking orders and distance of NMA molecule layers between the two crystals.
研究领域:
材料科学
·
化学
✓ 已验证
DOI
高影响因子
ACS Omega
·
2020
·
IF 2.87
Zhenghong Zhou,Kangfei Hu,Jiawei Wang,Zhibin Li,Yan Zhang,Zhenggen Zha,Zhiyong Wang
An electrochemical synthesis for quinazolines and quinazolinones was developed via a C(sp3)-H amination/C-N cleavage by virtue of the anodic oxidation. The reaction can be carried out in aqueous media under mild conditions to afford the desired products with high yields. The reaction mechanism was proposed after detailed investigation.
研究领域:
有机化学
·
电化学
✓ 已验证
DOI
高影响因子
Journal of Nano Research
·
2017
·
IF 0.511
Wen Juan Dong,Ji Yan Han,Xin Wu,Li Fan,Wen Ting Liang
A novel near-infrared fluorescence quenching method has been developed for the determination of hydrogen peroxide based on N-acetyl-L-cysteine-capped gold nanoparticles (NAC-AuNPs) as a fluorescence probe. The prepared gold nanoparticles with the size of about 1.91 nm exhibited strong near-infrared fluorescence emission at 693 nm with excitation wavelength at 450 nm in aqueous solution. The fluorescence intensity of NAC-AuNPs was quenched dramatically by adding hydrogen peroxide. Therefore, it could be used to detect hydrogen peroxide based on the fluorescence quenching intensity was linear with the concentration of hydrogen peroxide. Under the optimal experimental conditions, the linear range and detection limit were 1.0×10-6 –3.0×10-2 mol/L and 1.0×10-7 mol/L, respectively. The possible quenching mechanism was investigated by time-resolved fluorescence spectroscopy. The proposed method was simple, sensitive and showed good repeatability and stability.
研究领域:
分析化学
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生物医学工程
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纳米技术
✓ 已验证
DOI
高影响因子
JOURNAL OF CHEMICAL THERMODYNAMICS
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2017
·
IF 2.726
Dong Fu,Xue Feng,Pan Zhang
Amino acid ionic liquids (AAILs) including 1-butyl-3-methylimidazolium glycinate ([Bmim][Gly]), 1-butyl-3-methylimidazolium L -lysinate ([Bmim][Lys]) and tetramethylammonium glycinate ([N 1111 ][Gly]) were used to enhance the absorption of CO 2 in N -methyldiethanolamine (MDEA) aqueous solutions. The mole fractions of CO 2 in N 2 + CO 2 gas mixtures ranged from 0.2 to 1.0. The mass fractions of MDEA and AAILs respectively ranged from 0.300 to 0.400 and 0.050 to 0.100. The absorption capacity and absorption rate under series of conditions were presented and the influences of CO 2 partial pressure and the types of AAILs on the absorption performance were demonstrated.
研究领域:
化学工程
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环境科学
✓ 已验证
DOI
高影响因子
INORGANICA CHIMICA ACTA
·
2021
·
IF 2.545
Xingliang Li,Juncai Lu,Wanjun Mu,Baihua Chen,Daibing Luo,Bijun Liu,Yanqiu Yang,Hongyuan Wei,Shuming Peng
Nitrilotri–3–propanoic Acid (NTPA) and Tris(2–carboxyethyl) phosphine (TCEP) possess similar skeleton. This pair of isostructural ligands is a perfect set to assess the differences of uranyl (UO 2 2+ ) complexes with N–tricarboxylate versus P–tricarboxylate. The protonation reactions of NTPA and TCEP were investigated by potentiometry and calorimetry. Complexation of uranyl with the both ligands was studied by potentiometry and structural analysis. The results indicate that central trialkylamine in NTPA has a higher affinity for the proton than trialkylphosphine in TCEP. Crystal structures and NMR analyses indicate that central amine of NTPA and central phosphine of TCEP are not involved in the bonding. NTPA/UO 2 2+ complex is more stable than TCEP/UO 2 2+ complex. This difference cannot be explained by electronic effect of central N and P atoms because of nonbonding interactions. The higher stability of UO 2 2+ /NTPA versus UO 2 2+ /TCEP may be due to the fact that the central N atom of NTPA has a lower steric hindrance than the central P atom of TCEP. Another possible reason is that UO 2 2+ /TCEP complexes have different coordination modes from UO 2 2+ /NTPA complexes.
研究领域:
化学
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配位化学
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核化学
✓ 已验证
DOI
高影响因子
Environmental Science-Advances
·
2023
·Vol. 2
·期 5
·731-739
·
IF 0
Wen Wen,Yina Liu,Zhongping Li,Guangming Wen,Hung-Wing Li,Li Li
In this study, we report a simple pyrolytic strategy for N–C co-doped Fe-based nanoparticles (Fe–N–C) and exhibit their oxidase-mimicking and peroxidase-mimicking activity in a chromogenic reaction with 3,3′,5,5′-tetramethylbenzidine dihydrochloride (TMB) as a substrate. Structural analysis revealed that Fe–NX and Fe3C structures were formed with Fe-Imace coordination compounds as precursors and melamine as the nitrogen source, which provided abundant active sites for the Fe–N–C nanozyme. Interestingly, owing to the blocking effect triggered by π–π stacking between the tetracycline antibiotics (TCs) tetraphenyl skeleton and Fe–N–C, the substrate affinity of the Fe–N–C was significantly blocked, resulting in the solution fading. Under the optimum conditions, the UV absorption intensity versus the concentration of TCs was found to be linear over the range of 0.08–90 μM for tetracycline (TC), 0.1–80 μM for chlortetracycline (CTC) and 0.09–100 μM for oxytetracycline (OTC). The detection limits were 62 nM for TC, 85 nM for CTC and 88 nM for OTC. The Fe–N–C displayed good storage and long-term stability when stored at 4 °C for 30 days. In addition, based on its superparamagnetism, Fe–N–C can be effectively recycled and reused through an external magnetic field, avoiding secondary pollution.
研究领域:
分析化学
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生物医学工程
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环境科学
✓ 已验证
DOI
SENSORS AND ACTUATORS B-CHEMICAL
·
2023
·
IF 8.4
Zhijia Liao,Zhenyu Yuan,Hongliang Gao,Fanli Meng
In this study, porous sheet-like nanostructured Co 3 O 4 -CuO-CuOHF composites with great n-butanol sensing properties were synthesized by the biotemplate method and hydrothermal method . The effect of various contents of Co 3 O 4 -CuO-CuOHF sensor performance was systematically investigated, in which the best performance was achieved for the composite with 0.03 g Co 3 O 4 addition. The response of the best content Co 3 O 4 -CuO-CuOHF composite sensor to 100 ppm n-butanol at 180 ℃ is 120, which is 8 times higher than that of the CuO-CuOHF sensor. The composite sensor has excellent selectivity for n-butanol and responds 3.75–25 times higher to n-butanol than other target gases. It is detectable up to 500 ppb n-butanol and has potential promise for low concentration detection. Furthermore, it has outstanding stability and resistance to humidity. The gas sensing mechanism was analyzed by UV–visible diffuse reflectance spectroscopy, EPR oxygen vacancies and X-ray photoelectron spectroscopy, which indicated that the abundant oxygen vacancies , the physical adsorption of polar hydroxyl bonds, the electronegative fluorine substitution and the special microstructure of the composite contributed to its gas-sensitive performance.
研究领域:
材料科学
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纳米科技
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传感器技术
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表面化学
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功能材料
✓ 已验证
DOI
高影响因子
GREEN CHEMISTRY
·
2015
·Vol. 18
·期 6
·1731-1737
·
IF 8.02
Mengmeng Fan,Chunlin Zhu,Lin Liu,Qilu Wu,Qingli Hao,Jiazhi Yang,Dongping Sun
We have successfully prepared poly (3,4-ethylenedioxythiophene) (PEDOT)/N-doped reduced graphene oxide (N-rGO) by electrodeposition, post-reduction, and doping N atoms with a microorganism (as a green reagent) to modify PEDOT and resolve the exfoliation and fragmentation problems of pristine PEDOT. This modification greatly improves the electrochemical properties of PEDOT, showing great potential for a bio-electrode coating material, which should have excellent electrochemical properties, stability and biocompatibility. The as-prepared PEDOT/N-rGO shows lower impedance, and higher capacitive performance and cyclical stability than pristine PEDOT due to the doping of N-rGO. An MTT assay demonstrates this modified PEDOT has good adhesion, cell viability and proliferation, similar to pristine PEDOT. This indicates that the modification process does not restrain the good biocompatibility of pristine PEDOT, which results from the doping of highly biocompatible N-rGO by this green method. The wrinkled structure, residual oxygen containing functional groups and dopant N atoms of N-rGO lead to the formation of a fluctuating surface and an increase in the hydrophilicity of PEDOT, which increase the specific surface area and cell adhesion in cell culture, respectively. Consequently, this modified PEDOT improves the electrochemical properties, and resolves the exfoliation and fragmentation problems of pristine PEDOT, while still retaining the high biocompatibility of pristine PEDOT, which is promising for a bio-electrode coating material.
研究领域:
生物材料学
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电化学
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生物医学工程
✓ 已验证
DOI
高影响因子
CRYSTENGCOMM
·
2021
·Vol. 23
·期 25
·4549-4559
·
IF 3.545
Zongjian Liu,Zhicong Sun,Lin Zhang,Lifei Xu,Xinyue Lu,Qun Cui,Haiyan Wang
Hierarchical nanocrystal UiO-66 was synthesized by a template-free double solvent-modulated crystallization method. The influences of the ammonium hydroxide (NH4OH)/Zr and acetic acid (HAC)/Zr ratios and pH of reaction solution on the morphological and the porous properties of UiO-66 were investigated. The results show that the nanoscale grains of UiO-66 with the size of ∼20 nm and interparticle mesopores of ∼30 nm are obtained with the NH4OH/Zr of 0.96–3.84, HAC/Zr of 50 and the pH from 1.68 to 2.70. The introduction of NH4OH is favorable to the formation of Zr4+ oxo/hydroxo clusters and deprotonation of the ligands for accelerating the nucleation and crystallization, while HAC can effectively control the hydrolysis of zirconium chloride to avoid the formation of particles with low crystallinity. The equilibrium adsorption capacities of nHEP and MCH on UiO-66(2.88, 50) are higher than that on UiO-66-AS at 323–373 K, respectively. The effective diffusion coefficients of n-heptane/methyl cyclohexane on the hierarchical UiO-66 nanocrystals are about 5 and 18 times higher than that on microporous UiO-66 at 373 K and 0.05–6 kPa, respectively. The introduction of mesopores increases the adsorption performance of the adsorbent for alkanes and enhances mass transfer.
研究领域:
材料科学
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化学工程
✓ 已验证
DOI
高影响因子
International Journal of Extreme Manufacturing
·
2022
·Vol. 5
·期 1
·015502
·
IF 10.036
Zhibin Jiang,Lujie Jin,Xiying Jian,Jinxia Huang,Hongshuai Wang,Binhong Wu,Kang Wang,Ling Chen,Youyong Li,Xiang Liu,Weishan Li
Lithium-sulfur (Li-S) batteries can provide far higher energy density than currently commercialized lithium ion batteries, but challenges remain before it they are used in practice. One of the challenges is the shuttle effect that originates from soluble intermediates, like lithium polysulfides. To address this issue, we report a novel laminar composite, N,O-carboxymethyl chitosan-reduced graphene oxide (CC-rGO), which is manufactured via the self-assembly of CC onto GO and subsequent reduction of GO under an extreme condition of 1 Pa and −50 °C. The synthesized laminar CC-rGO composite is mixed with acetylene black (AB) and coated on a commercial polypropylene (PP) membrane, resulting in a separator (CC-rGO/AB/PP) that can not only completely suppress the polysulfides penetration, but also can accelerate the lithium ion transportation, providing a Li-S battery with excellent cyclic stability and rate capability. As confirmed by theoretic simulations, this unique feature of CC-rGO is attributed to its strong repulsive interaction to polysulfide anions and its benefit for fast lithium ion transportation through the paths paved by the heteroatoms in CC.
研究领域:
材料科学
·
能源存储技术
·
电化学
✓ 已验证
DOI
高影响因子
Catalysts
·
2022
·Vol. 12
·期 6
·640
·
IF 4.501
Xu Lu,Chenhao Wei,Liang Zhao,Jinsen Gao,Chunming Xu
Coke formation on n-butene cracking catalyst is the main reason for the reducing of its lifetime. To study the effects of acidity and textural properties on the coke formation process, a series of HY zeolite-type catalysts were prepared by ammonium hexafluorosilicate treatment (AHFS). NH3-TPD and Py-IR-TPD were used to systematically study the change law of zeolite acidity. It was found that with the increase of AHFS concentration, the acid density decreased, whereas the ratio of Brønsted acid to Lewis acid first increased and then decreased. Meanwhile, the percentage of Brønsted acid inside the supper cages increased and the strength of Brønsted acid increased with the degree of dealumination. Combined with in situ IR study on coke formation, the relationship between coking and acid site was revealed. It was found that the rate of coke formation on zeolites was affected by acid density, which is the rate of coke formation decreased with the decline of acid density. When the acid density remains at the same level, it was the acid strength that determined the coke formation rate—the stronger the acid strength, the faster the coke formation rate.
研究领域:
催化化学
·
材料科学
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2023
·Vol. 11
·期 8
·4088-4101
·
IF 11.9
Tian Yu,Suiting Ning,Tingting Zhang,Xiangbin Chen,Qian Liu,Ning Qi,Zhiquan Chen,Xianli Su,Xinfeng Tang
As one kind of superionic conductor, CuAgSe is a promising thermoelectric material due to its extremely low thermal conductivity and high electron mobility. In this study, the electrical and thermal properties of CuAgSe were collaboratively optimized by changing the chemical composition. Seebeck coefficient measurements reveal that stoichiometric and CuAg-deficient CuAgSe materials show n–p transition with the increase of temperature. In contrast, the Se-deficient CuAgSe still shows n-type conduction in the α-phase at high temperatures. Positron annihilation measurements indicate that there are large amounts of cation vacancies such as Ag and Cu vacancies in the stoichiometric and CuAg-deficient samples, which provide a high concentration of hole carriers and are responsible for the n–p transition at high temperatures. The number of vacancies decreases gradually with increasing CuAg content, and in the Se-deficient CuAgSe, VAg–Se divacancies are formed, which further results in a sufficient decrease of hole carriers. As a result, the Se-deficient samples still show n-type conduction in the α phase. Our results indicate that vacancy defects are the key factors that determine the conduction type in CuAgSe, which can be tuned by the chemical composition. In addition, superb thermoelectric performance was achieved in both p-type and n-type CuAgSe, with maximum ZT of 0.96 at 573 K in (CuAg)0.96Se (p-type) and 0.55 at 630 K in (CuAg)1.02Se and (CuAg)1.04Se (n-type).
研究领域:
材料科学
·
热电学
·
固体物理学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）