ChemCatChem
·
2021
·Vol. 14
·期 6
·e202101539
·
IF 5.686
Siwei Zhao,Shaohua Jin,Huanmin Liu,Youxin Su,Wei Liu,Shengfu Li,Chongchong She,Haonan Li,Kun Chen
Graphical A series of all-inorganic lead-free halide perovskite inverse opals were prepared and furtherly used as the photocatalysts to promote the polymerization of EDOT under the irradiation of visible light. All the samples exhibited the nice replica of the artificial template and high crystallinity. The bandgap of the catalysts was adjusted by screening the ratios of bromide to iodide and antinomy to bismuth. Cs 3 Bi 0.5 Sb 1.5 Br 9 showed the highest performance of the photocatalytic polymerization for EDOT, indicating the dual halide perovskites are more flexible than single halide perovskite in terms of bandgap engineering. A series of all-inorganic lead-free halide perovskite inverse opals were prepared and furtherly used as the photocatalysts to promote the polymerization of 3, 4-ethylenedioxythiophene (EDOT) under the irradiation of visible light. All the samples exhibited the nice replica of the artificial template and high crystallinity. The bandgap of the catalysts was adjusted by screening the ratios of bromide to iodide and antinomy to bismuth, respectively. Among all the samples, Cs 3 Bi 0.5 Sb 1.5 Br 9 inverse opal showed the best catalytic performance and the excellent stability in terms of the morphology and the crystalline phase after four cycles of photocatalytic polymerization. Since EDOT is commercially available, the present observation suggested a convenient protocol of preparing the composited materials or optoelectronic devices based on the lead-free halide perovskites and the conductive poly(3, 4-ethylenedioxythiophene).
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高影响因子
CERAMICS INTERNATIONAL
·
2021
·
IF 4.527
Nali Li,Yong Yu,Yanwei Tong,Tiantian Liu,Xuefeng Zhang
An enhanced sol-gel combustion method was used to synthesize different porous Sc 3+ -doped Li 3 V 2-x Sc x (PO 4 ) 3 /C (x = 0.00, 0.05, 0.10 and 0.15) compounds. The substitution of Sc 3+ into the V 3+ sites of Li 3 V 2-x Sc x (PO 4 ) 3 /C expands the lattice volume along with the enlargement of Li + diffusion channel, which is beneficial for Li + transportation and ionic conductivity improvement. Besides, the Sc 3+ doping content exhibits a great impact on the morphology of Li 3 V 2-x Sc x (PO 4 ) 3 /C composite. The pristine Li 3 V 2 (PO 4 ) 3 /C are constituted of porous particles and nanorods , and the ratio of nanorods to particles can be controlled by adjusting the amount of Sc 3+ doping since the ratio of nanorods to particles decreases with increasing Sc 3+ doping content. When Sc 3+ doping content increases to a certain level (x = 0.15, Li 3 V 1.85 Sc 0.15 (PO 4 ) 3 /C), the nanorods are hardly seen. Li 3 V 1.90 Sc 0.10 (PO 4 ) 3 /C with higher tapped density, better reversibility, smaller resistance and larger Li + diffusion coefficient demonstrates outstanding rate performance and cyclic stability, together with high specific discharge capacities of 130.2 and 92.9 mAh g −1 at 0.5 and 20 C, respectively. Furthermore, a superior specific discharge capacity of 85.8 mAh g −1 was retained at 20 C following 1000 cycles. Overall, a novel approach for the preparation of high-performance Li 3 V 2-x Sc x (PO 4 ) 3 /C cathodes with different morphologies for lithium-ion batteries is provided.
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高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2024
·Vol. 31
·期 14
·21430-21441
·
IF 0
Jiang Changjin,Zhang Shuang,Zhang Ting
Fe 3+ complexed with 3-aminopropyltriethoxysilane (APTES)-modified carboxymethyl chitosan (CMC) named Fe-ACMC was synthesized by a one-step method at room temperature and pressure. The surface morphology and chemical structure of Fe-ACMC were characterized by SEM-EDS, XRD, BET, FT-IR, XPS, and ζ-potential. In batch adsorption, the optimum pH for arsenate [As(V)] adsorption onto Fe-ACMC was 3–9 with removal efficiency > 99%. The adsorption of As(V) could reach equilibrium within 25 min and the maximum adsorption capacity was 84.18 mg g –1 . The pseudo-second-order model fitted well the kinetic data ( R 2 = 0.995), while the Freundlich model well described the adsorption isotherm of As(V) on Fe-ACMC ( R 2 = 0.979). The co-existing anions (NO 3 – , CO 3 2– , and SO 4 2– ) exhibited a slight impact on the As(V) adsorption efficiency, whereas PO 4 3– inhibited As(V) adsorption on Fe-ACMC. The real applicability of Fe-ACMC was achieved to remove ca. 10.0 mg L –1 of As(V) from natural waters to below 0.05 mg L –1 . The regeneration and reuse of Fe-ACMC for As(V) adsorption were achieved by adding 0.2 mol L –1 HCl. The main adsorption mechanism of As(V) on Fe-ACMC was attributed to electrostatic attraction and inner-sphere complexation between –NH 2 ···Fe 3+ and As(V). In fixed-bed column adsorption, the Thomas model was the most suitable model to elucidate the dynamic adsorption behavior of As(V). The loading capacity of the Fe-ACMC packed column for As(V) was 47.04 mg g –1 at pH 7 with an initial concentration of 60 mg L –1 , flow rate of 3 mL min –1 , and bed height of 0.6 cm. Graphical abstract
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PubMed
DYES AND PIGMENTS
·
2018
·
IF 3.767
Xiao-Lei Zhao,Jiao Geng,Bin Hu,Dan Xu,Wei Huang
New monomethine dyes have been prepared by a simple and highly efficient method in acetic anhydride, in which the common pyridine-2,6-dione moiety and thiophene derivatives occupy each side of the methine unit. Among them, the ternary monomethine-azo dyes were first obtained by the particularly useful post-modification synthetic strategy, in order to further adjust the π -conjugated system and electronic spectra of 2-amino-3-cyano-4-chloro-5-formylthiophene based heterocyclic hydrazone/azo dyes. UV−Vis spectral analyses reveal that the synthesized heterocyclic dyes exhibit a large color gamut because of the extension of the conjugation length of the chromophore , where the maximum absorption wavelength ( λ max ) is significantly red-shifted up to 181 nm from binary monomethine to ternary monomethine-azo dyes.
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高影响因子
Materials Research Express
·
2023
·Vol. 10
·期 7
·076301
·
IF 2.3
Xiangcheng Cai,Peng Tu,Yansong Ai,Hongshen He,Peng Shen,Yuanming Zhou,Fei Mei
Multi-color light-emitting materials are essential lighting and displays. In this study, mixed halide system was applied to precisely tune the bandgap of CH3NH3Pb(BrxI1-x)3, thus regulating the emission wavelength. PEABr was employed to change the phase structure and morphology of CH3NH3Pb(BrxI1-x)3 perovskite thin films and improve the performance of multi-color perovskite light-emitting diodes (PeLEDs). Theoretical simulations through first-principles calculations and experiments demonstrate that multi-color PeLEDs can be achieved by adjusting the ratio of bromine (Br) and iodine (I) atoms in the CH3NH3Pb(BrxI1-x)3 perovskite. The maximum luminance of PEABr-modified green PeLEDs reached 7108 cd m−2, with a maximum current efficiency of 8.25 cd A−1 and a maximum external quantum efficiency (EQE) of 1.62%, which were greatly improved compared to the reference device without PEABr. In addition, the luminance of orange-yellow and red mixed-halide PeLEDs both exceed 100 cd m−2. The results demonstrate that the use of PEABr additive can effectively control the morphology of CH3NH3Pb(BrxI1-x)3 crystals, and high-performance multi-color light-emitting devices can be achieved by combining with mixed halide system. The electroluminescence spectra showed that the emission range of the devices covered the wavelength region of 520–720 nm, demonstrating their good application prospects in the field of multi-color displays.
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高影响因子
THERMOCHIMICA ACTA
·
2016
·
IF 1.938
X.K. Gao,X. Wen,H. Zhou,Q. Zhu,J.L. Wang,X.Y. Li
In this work, a novel and simple method was put forward to measure the isobaric specific heat capacity for the kerosene RP-3 with a flow-calorimeter at the conditions of high temperature and high pressure. Based on the energy conservation principle, the formula for heat capacity was derived and its measurement was realized by the convective mixing method between the hot and cold fuel. Taking the precision of the instrument and the error transfer into account, the relative expanded uncertainty of this method was acquired of about ± 6.38% (coverage factor k = 2). Meanwhile, the accuracy and reliability were verified by the standard material of water and n -decane. In the temperature range from (296.2–719.0) K and under pressure range from (2.4–4.0) MPa, the measurement for the kerosene RP-3 was carried out and the experimental observations were compared and agreed well with the published data. At last, an empirical correlation relationship of heat capacity due to the temperature and pressure was presented by using Garg’s model with the measured experimental data.
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高影响因子
Inorganic Chemistry Frontiers
·
2018
·Vol. 5
·期 3
·619-625
·
IF 5.106
Ying Liu,Maxim S. Molokeev,Quanlin Liu,Zhiguo Xia
Crystal structure evolution and temperature-dependent phase transition of solid solutions are much desired for the understanding of the optimization of functional properties. Herein, the NASICON-type NaZr2(PO4)3–SrZr4(PO4)6 solid solutions with the formula Na(2−2x)Srx[ ]xZr4(PO4)6 (0 ≤ x ≤ 1), where [ ] represents the vacancy, were prepared by the sol–gel method, and their crystal structures, phase transitions and thermal expansion properties were investigated in detail. In the range of x = 0.3–0.35, there is a reversible structural phase transition Rc ↔ R and the different structural models of the R phase and Rc phase were built to better understand the phase transition mechanism. We determined the phase transition boundary between the Rc and R structures and predicted the phase transition temperature of Na(2−2x)Srx[ ]xZr4(PO4)6 with any x for further investigation of controlled physical properties. The results indicated that Na0.5Sr0.75[ ]0.75Zr4(PO4)6 showed a near zero thermal expansion in the temperature range of 450–600 K, which can find potential applications.
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高影响因子
JOURNAL OF POWER SOURCES
·
2018
·
IF 6.945
Na Wang,Gaoyi Han,Hua Song,Yaoming Xiao,Yanping Li,Ying Zhang,Hongfei Wang
Thin layers of continuous gold have been deposited on the both sides of porous polypropylene films (PPF) via electroless plating method to form a sandwich structure with two conductive surfaces and an intermediate insulating layer (Au/PPF/Au). Then poly (3, 4-ethylenedioxy thiophene) (PEDOT) layers are electrodeposited on the two conductive sides via cyclic voltammetry method to form the sandwich-structured PEDOT-Au/PPF/Au-PEDOT. Gel electrolyte of H 3 PO 4 /polyvinyl alcohol (H 3 PO 4 /PVA) is then added to the sandwich-structured PEDOT-Au/PPF/Au-PEDOT to form the integrated flexible supercapacitor of Au-PEDOT|H 3 PO 4 /PVA|PEDOT-Au. The PEDOT-Au/PPF/Au-PEDOT sandwiched structures are characterized and the capacitive performances of the integrated flexible cells are investigated in detail. The results show that the optimum integrated flexible cell exhibits excellent cycling stability (91.8% capacitance retention after 20000 cycles) and relatively high areal specific capacitance. Furthermore, the cells of Au-PEDOT|H 3 PO 4 /PVA|PEDOT-Au not only exhibit excellent bending endurance (99.1% capacitance retention after 5000 repeated bending cycles), but also can be conveniently connected in series without additional wires. This integrated flexible cell may exhibit potential application in portable electronics.
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高影响因子
JOURNAL OF NANOPARTICLE RESEARCH
·
2015
·Vol. 17
·期 8
·1-13
·
IF 2.184
Qin Jianbin,Zhang Guangcheng,Shi Xuetao,Tao Min
The dispersions was prepared by dispersing hydrophilic silica nanoparticles with an average diameter of 50 nm in 1-butyl-methylimidazolium tetrafluoroborate ([C 4 mim][BF 4 ]), and investigated under the steady shear and oscillatory shear, respectively. Experimental results indicate that all of the dispersions present shear thinning, notable shear thickening, and shear thinning successively with increasing shear rate; the shear thickening behavior is derived from silica nanoparticle clusters and strongly controlled by silica nanoparticle content and temperature. The shear thickening fluid (STF) exhibits reversible property and transient response ability, and the time of transient response is no more than 100 ms. The conductivity of the STF is increased with increasing silica nanoparticle content, and the conductivity of 27 wt% dispersions is even two times as big as that of pure [C 4 mim][BF 4 ]. The dispersions with high solid content dilate and present a phase transition changing from a liquid-like to a solid-like soft material in the shear thickening region. A theoretical model is developed to imitate the mechanism of shear thickening in the dispersions.
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高影响因子
PROCESS BIOCHEMISTRY
·
2020
·
IF 2.952
Yuan Lu,Hongqian Dai,Hanbing Shi,Lan Tang,Xingyuan Sun,Zhimin Ou
Fe 3 O 4 -Arg was selected as the optimal carrier due to its high activity recovery of immobilized cells in the preparation of Fe 3 O 4 -Arg-Cells. The optimal immobilization conditions for the preparation of Fe 3 O 4 -Arg-Cells were 30 °C, 4 h, pH 7, and 3 g dry yeast. The activity recovery of immobilized cells reached 76.8 %. For a batch reduction in a shaker in an alternating magnetic field, Fe 3 O 4 -Arg-Cells were used as a catalyst to gain ethyl ( R )-4-chloro-3-hydroxybutyrate (( R )-CHBE). For further improvement in reduction productivity, a continuous reduction in the magnetic fluidized bed reactor system (MFBRS) was completed. Under their optimal transformation conditions, it took 24 h for Fe 3 O 4 -Arg-Cells to complete the conversion of ethyl 4-chloro-3-oxobutanoate (COBE) (0.8553 mol/L) in the shaker and only 8 h for the batch reduction in an alternating magnetic field. Continuous reduction in MFBRS provided new ideas for the efficient production of ( R )-CHBE; 1.5882 mol/L (10 mL) of COBE can be completely converted in 6 h. The conversion and enantiomeric excess (e.e.) of ( R )-CHBE were 100 % and above 99.9 % respectively, in the three reaction systems mentioned above.
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高影响因子
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2018
·Vol. 102
·期 7
·4092-4102
·
IF 2.956
Yunhui Zhang,Haitao Wu
La 2 (Zr 1− x Ti x ) 3 (MoO 4 ) 9 (0 ≤ x ≤ 0.1) ceramics were prepared by the traditional solid-state reaction method. XRD analysis showed that La 2 (Zr 1− x Ti x ) 3 (MoO 4 ) 9 (0 ≤ x ≤ 0.1) ceramics belonged to a trigonal system. Based on the chemical bond theory, the consequences of bond energy, bond ionicity, lattice energy, and thermal expansion coefficient of ceramics on microwave dielectric properties were discussed. As Ti 4+ addition was increased, the reduction in dielectric constant was ascribed to the fact that the polarizability of Ti 4+ is smaller than Zr 4+ , and the downward trend was related to the bond ionicity. Besides, the tendency of Q·f value depended on the packing fraction and the lattice energy. The improvement in τ f value, the increase in bond energy, and the decrease in the coefficient of thermal expansion were all correlated. The far-infrared spectra implied that the absorptions of structural phonon oscillation were the main reason for the maximum polarization contribution. La 2 (Zr 0.92 Ti 0.08 ) 3 (MoO 4 ) 9 ceramics sintered at 750°C for 4 hours exhibited the best dielectric properties ( ε r = 10.33, Q·f = 80 658 GHz, and τ f = 3.48 ppm/°C).
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高影响因子
Journal of Materials Chemistry C
·
2018
·Vol. 6
·期 22
·5908-5915
·
IF 5.976
Gaoliang Fang,Daqin Chen,Su Zhou,Xiao Chen,Lei Lei,Jiasong Zhong,Zhenguo Ji
Successful development of all-inorganic CsPbX3 (X = Cl, Br, or I) perovskite quantum dots (PQDs) has been witnessed due to their unique optical and electrical properties. However, the heavy usage of Pb element in PQDs has limited the commercial application of these PQDs, and the preparation of low-Pb or Pb-free PQDs is imperative. In this study, we report room-temperature reverse synthesis of CsPbxMn1−xCl3 PDQs from CsMnCl3 precursor nanocrystals through cation exchange. Interestingly, two-step phase transformation processes from hexagonal CsMnCl3 to rhombohedral Cs4PbxMn1−xCl6 and finally to cubic CsPbxMn1−xCl3 are evidenced. With an increase in the reaction time, Mn2+ ions in the PQD lattice are gradually replaced by Pb2+ ions. Notably, Mn2+ d → d broadband luminescence is not detected for the Cs4PbxMn1−xCl6 product, but it is intense for the CsPbxMn1−xCl3 sample owing to efficient energy transfer from CsPbCl3 to Mn2+. Moreover, it is found that the introduction of Br− into the reaction system will prohibit the complete phase transformation from rhombohedral Cs4PbxMn1−x(Cl/Br)6 to cubic CsPbxMn1−x(Cl/Br)3. By controlling the ratio between the CsMnCl3 precursor and PbBr2, tunable luminescence is easily achieved due to the combined emissions from both CsPb(Cl/Br)3 PQDs and Mn2+-emitting centers.
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高影响因子
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