JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
·
IF 9.965
Ping Bai,Peng Wang,Yuhang Wu,Xin Pang,Meiting Song,Chunfang Du,Yiguo Su
A series of Zn m In 2 S 3+m photocatalysts were synthesized to show tunable band gap energy with the variation of Zn/S atomic ratio. The junction of Zn m In 2 S 3+m and BiVO 4 led to intimate interfacial contacts. Both experimental and theoretical results implied that electrons flowed from Zn m In 2 S 3+m to BiVO 4 at the Zn m In 2 S 3+m /BiVO 4 interface to form built-in electric field due to the variation of Fermi level, which promised Z scheme charge transfer feature for improving separation of charge carriers for enhanced photocatalytic performance. A higher degree of charge transfer process occurred for Zn 2 In 2 S 5 /BiVO 4 heterostructure promised stronger built-in electric field, higher charge separation efficiency and improved photocatalytic activity in comparison to ZnIn 2 S 4 /BiVO 4 and Zn 3 In 2 S 6 /BiVO 4 heterojunctions . The optimal hydrogen production rate of Zn 2 In 2 S 5 /BiVO 4 photocatalyst is 8.42 mmol•g −1 •h −1 with apparent quantum yield of 22.32 % at 435 nm, which is about 2.2 and 1.5 times higher than that of ZnIn 2 S 4 /BiVO 4 and Zn 3 In 2 S 6 /BiVO 4 , respectively.
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高影响因子
FUEL
·
2022
·
IF 8.035
Minghao Zhou,Yaqi Xue,Fei Ge,Jing Li,Haihong Xia,Junming Xu,Jun Zhao,Changzhou Chen,Jianchun Jiang
MOF-derived Ni-based bimetallic catalysts were found to be effective for the in-situ hydrogenation/hydrodeoxygenation of lignin-derived monophenols and dimers with isopropanol as the hydrogen-donor solvent (without external hydrogen). The synergistic effects of bimetallic catalysts were studied, and their catalytic properties afforded the best conversion rate of phenols and cyclohexanol/cycloalkane yields. The detailed physicochemical characterization was conducted by means of XRD, H 2 -TPR, NH 3 -TPD, and pyridine-IR analysis. The effects of reaction temperature (200–260 ℃) and reaction time (2–5 h) on the performance of lignin-derived monophenols and dimers were investigated. During the in-situ hydrogenation/hydrodeoxygenation of lignin-derived phenols, the steric effects and the effects of various functional groups, notably methoxy groups, were investigated. In-situ conversion of lignin-derived phenols with isopropanol was achieved over different Ni/M ratios of NiM@C (M = Co, Mo, and La) catalysts, from which NiLa 0.33 @C produced satisfactory yields of cyclohexanol/cycloalkanes.
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CRYSTENGCOMM
·
2022
·Vol. 24
·期 21
·3852-3858
·
IF 3.756
Runze Guo,Yufeng Liu,Yongzheng Fang,Zhifu Liu,Langping Dong,Lei Wang,Wenyao Li,Jingshan Hou
CsPbI3 has the least chemical stability among the CsPbX3 (X = Cl, Br, and I) perovskite nanocrystal (PNC) family due to its thermodynamically metastable characteristics, thus limiting the development of all-inorganic perovskite white-light devices. The current study presents a microfluidic-based continuous large-scale fabrication of CsPbI3-mesoporous SiO2 (CPI/m-SiO2) nanocomposites to solve the problem of large-scale continuous production of stable, repeatable, high-quality perovskite NCs. The results reveal that the chemical stability and thermal quenching behaviour of CPI PNCs were greatly improved due to the protection of mesoporous silica. Particularly, the water resistance property of CPI/m-SiO2 nanocomposites improved two-fold compared to that of noncomposite CPI PNCs, and the thermal stability of the CPI/m-SiO2 nanocomposites improved nearly three-fold at 373 K when compared with that of the noncomposite CPI NCs. Furthermore, photons were speculated to transmit along with the pores and channel structure of m-SiO2 to reduce photon absorption between NCs. Moreover, the microfluidic technology can operate continuously and is precisely controllable, enabling large-scale nanocomposite synthesis with uniform size and shape.
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JOURNAL OF RARE EARTHS
·
2022
·
IF 4.632
Pan Liang,Lianqing Li,Tong Shen,Wenli Lian,Zhihong Liu
In this work, through a facile method of low-temperature (only 350 °C) self-reduction, 1D nano-sized M 2 B 5 O 9 Cl:Eu 2+ (M = Sr, Ca) blue phosphors with highly efficient performance can be obtained. The crystal structure, morphology and photoluminescence (PL) properties including thermal stability of M 2 B 5 O 9 Cl:Eu 2+ (M = Sr, Ca) phosphors were investigated. The M 2 B 5 O 9 Cl:Eu 2+ (M = Sr, Ca) phosphors show broad band excitation spectra and narrow band emission spectra . The photoluminescence quantum yields (PLQY) of M 2 B 5 O 9 Cl:Eu 2+ (M = Sr, Ca) are as high as 98% and 87.2%, respectively. Furthermore, the color purities of M 2 B 5 O 9 Cl:Eu 2+ (M = Sr, Ca) can reach 99.1% and 93.2%, respectively. When heated up to 150 °C, the emission intensities of M 2 B 5 O 9 Cl:Eu 2+ (M = Sr, Ca) phosphors can still keep 72.7% and 80.0%, respectively. Finally, the above-mentioned phosphors exhibit outstanding performance when manufacturing WLEDs.
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JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
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2023
·
IF 3
Guorong Ma,Pengzheng Luo,Ruiqiang Xu,Rui Ma,Lei Qiu,Chenran Xu,Rang Yang,Yating Li,Zhihao Zhao,Ling Huang,Yanhui Yang,Pei Wang
M. tuberculosis is the most successful intracellular pathogen and remains a major threat to human health. It is crucial to investigate the profile of cytoplasmic proteins from M. tuberculosis for pathogenesis, clinical markers, and protein vaccine development. In this study, six biomimetic affinity chromatography (BiAC) resins with high differences were selected for M. tuberculosis- cytoplasmic protein fractionation. All fractions were identified using liquid chromatography-mass spectrometry (LC-MS/MS) analysis. A total of 1246 M. tuberculosis proteins were detected (p < 0.05), among which 1092 M. tuberculosis proteins were identified in BiAC fractionations and 714 M. tuberculosis proteins in un-fractionations (Table S1.3.1). The majority of 66.8% (831/1246) identifications were distributed in the range of Mw 7.0–70.0 kDa, pI 3.5–8.0, and Gravy values <0.3. Furthermore, 560 M. tuberculosis proteins were detected in both the BiAC fractionations and un-fractionations. Compared with the un-fractionations, the average number of prot_matches, prot_cover, prot_sequence, and emPAI values of these 560 proteins in the BiAC fractionations were increased by 3.791, 1.420, 1.307, and 1.788 times, respectively. Overall, compared with un-fractionations, the confidence and profile of M. tuberculosis cytoplasmic proteins were improved by BiAC fractionations coupled with LC-MS/MS analysis. The strategy of BiAC fractionation can be used as an effective method for pre-separating protein mixtures in proteomic studies.
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高影响因子
JOURNAL OF CHEMICAL AND ENGINEERING DATA
·
2021
·
IF 2.694
Yangyi Huang,Yuning Zhang,Haoran Liu,Weiping Luo
In this study, the solubilities of isophthalic acid (IPA) in N-methylformamide (NMFM), N-methylformanilide (NMFL), propanoic acid (PA), sulfolane, and dimethyl sulfoxide (DMSO) and m-toluic acid (m-TA) in acetone, cyclohexanone (CYC), 1-methyl-2-pyrrolidinone, NMFM, NMFL, N,N-dimethylformamide, PA, sulfolane, and DMSO were determined by the dynamic laser method at atmospheric pressure (101.2 kPa), and the solubility ratios between IPA and m-TA in different solvents were calculated. The temperature range of the experiment was between 290.15 and 348.15 K, in which the solubilities of IPA and m-TA in selected solvents were positively correlated with temperature. The maximum ratio between the mole fraction of solubilities of m-TA and IPA was in CYC and ranged from 68 to 84 for the temperature range under study. The experimental data were correlated by the Apelblat model, the Buchowski–Ksiazczak λh model, and the modified nonrandom two-liquid (NRTL) activity coefficient model.
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
·
2021
·
IF 5.302
Bing Liu,Ke Sha,Meng Fei Zhou,Kai Xin Song,Yu Hui Huang,Cheng Chao Hu
Two novel low- ε r gallates MGa 2 O 4 (M = Ca, Sr) have been synthesized via a standard solid-state reaction method. According to the X-ray diffraction results, CaGa 2 O 4 crystallizes in space group Pna2 1 with an orthorhombic symmetry, while SrGa 2 O 4 belongs to the monoclinic P2 1 / c system. Both ceramics show ever-improving microstructures with the increasing sintering temperature . The optimal microwave dielectric properties ( ε r = 9.2, Qf = 66,000 GHz, τ f =–85 ppm/°C for SrGa 2 O 4 and ε r = 10.6, Qf = 15,400 GHz, τ f =–58 ppm/°C for CaGa 2 O 4 ) are obtained when sintered at 1275 °C. A patch antenna is fabricated using SrGa 2 O 4 ceramics as the substrate, which realizes a return loss of –19.94 dB and total efficiency of –1.38 dB (72.8 % in power ratio) at 4.84 GHz. The exceptional performances indicate that SrGa 2 O 4 ceramics are promising candidates for antenna applications at the Sub-6 GHz band.
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CRYSTENGCOMM
·
2021
·Vol. 23
·期 39
·6899-6908
·
IF 3.545
Huimin Wang,Tingting Wang,Zibin Huang,Yizhuo Liu,Dehui Leng,Junli Wang
The growth of metal chalcogenide nanowires (NWs) on metal substrates is challenging work since the direct reactions taking place between the chalcogen (S, Se or Te) and zero-valent metal (M0) are frequently unable to regulate the crystallization of nanocrystals in an anisotropic one-dimensional (1D) manner. We here report the use of Ag2Se seeds as catalyst particles to realize the growth of metal selenide (MSe) NWs on their respective metal foil or flakes, including ZnSe/Zn, CdSe/Cd, and MnSe/Mn material systems. Metal foil or flakes (M = Zn, Cd and Mn) serve as a support substrate as well as a metal cation source during the NW synthesis. The preformed Ag2Se seeds play the roles of not only catalytic particles that initiate a so-called solution–solid–solid process to produce crystalline MSe NWs on metal substrates, but also inert impurities that promote an electrochemical anodic reaction of the metal to supply metal cations (M0 − 2e → M2+) for the NW formation. The microstructural studies by HRTEM reveal the polytypism and particularly the diameter-dependence of crystal phases and growth directions in the resulting MSe NWs, which can be rationalized from the viewpoints of the energetics and the catalyst/NW interfacial structures. These semiconductor NWs grown on metal foil or flakes may find wide use in photoelectric catalysis and devices without a transfer process of free-standing NWs onto a conductive support substrate.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2020
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IF 4.65
Quanli Hu,Bin Yue,Hongyang Shao,Fan Yang,Jinghui Wang,Yin Wang,Jinghai Liu
Lanthanum-based LaMO 3 (M = Fe, Co, Ni) perovskite nanofibers were effectively fabricated by electrospinning approach coupled with calcination process. The crystallinity, microstructures, morphologies, elemental compositions, and chemical bonding states of LaMO 3 perovskites were investigated in detail. The electrochemical properties of LaMO 3 perovskite nanofibers as supercapacitor electrodes and lithium-ion battery anodes were elucidated. The specific capacitances of LaFeO 3 , LaCoO 3 , and LaNiO 3 nanofibers were 183.6, 95.8 and 116.3 F g −1 at the current density of 1 A g −1 , respectively. The supercapacitive properties of LaMO 3 NFs had originated from the redox reactions of M 3+ /M 2+ . As lithium-ion battery anodes, LaMO 3 (M = Fe, Co, Ni) nanofibers exhibited the specific discharge capacities of 331, 646, and 92 mAh g −1 after 200 cycles, respectively. This research endowed the potential and competent candidates of the perovskite type lanthanum-based nanofibers for supercapacitor electrodes and lithium-ion battery anodes.
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RSC Advances
·
2021
·Vol. 11
·期 37
·22780-22788
·
IF 3.361
Xiaoyi Sun,Qingjie Liu,Shuai Liu,Xintang Zhang,Shanshan Liu
A series of MOx–Cr2O3–La2O3/TiO2–N (M = Cu, Fe, Ce) catalysts with nitrogen doping were prepared via the impregnation method. Comparing the low-temperature NH3-SCR activity of the catalysts, CeCrLa/Ti–N (xCeO2–yCr2O3–zLa2O3/TiO2–N) exhibited the best catalytic performance (NO conversion approaching 100% at 220–460 °C). The physico-chemical properties of the catalysts were characterized by XRD, BET, SEM, XPS, H2-TPR, NH3-TPD and in situ DRIFTS. From the XRD and SEM results, N doping affects the crystalline growth of anatase TiO2 and MOx (M = Cu, Fe, Ce, Cr, La) which were well dispersed over the support. Moreover, the doping of N promotes the increase of the Cr6+/Cr ratio and Ce3+/Ce ratio, and the surface chemical adsorption oxygen content, which suggested the improvement of the redox properties of the catalyst. And the surface acid content of the catalyst increased with the doping of N, which is related to CeCrLa/TiO2–N having the best catalytic activity at high temperature. Therefore, the CeCrLa/TiO2–N catalyst exhibited the best NH3-SCR performance and the redox performance of the catalysts is the main factor affecting their activity. Furthermore, in situ DRIFTS analysis indicates that Lewis-acid sites are the main adsorption sites for ammonia onto CeCrLa/TiO2–N and the catalyst mainly follows the L–H mechanism.
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高影响因子
Journal of Rubber Research
·
2019
·Vol. 23
·期 1
·41-46
·
IF 0.281
Liao Xiao-Xue,Wei Yan-Chan,Zhang Hui-Feng,Zheng Ting-Ting,Luo Ming-Chao,Liao Shuangquan
Waste rubber with three-dimensional structure is insoluble and non-melting, which creates recycling problem. The technique called “high-pressure high-temperature sintering” (HPHTS) can convert vulcanized rubber powder into usable rubber products. However, reversion occurs when vulcanizates are exposed to a prolonged treatment at high temperature. This reversion results in the decrease of mechanical properties of sintered waste rubber powder (WRP) samples. To address this problem, a method of enhancing the mechanical properties of sintered WRP by incorporating different content of maleic anhydride (MA) and N , N ′- m -phenylene bismaleimide (BMI) is discussed in this paper. The results show that BMI and MA can slow down the formation of the conjugated double bonds. Through Diels–Alder reaction, BMI inhibits conjugated double bonds formation and improves the adhesion between particles and particles, which is beneficial to improvement of final properties. Therefore, BMI improves the mechanical properties of sintered WRP greatly.
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
·
2019
·
IF 4.029
Changzhi Yin,Ying Tang,Junqi Chen,Feihu Li,Yijun Huang,Chunchun Li,Xianran Xing,Liang Fang
Two melilite ceramics Sr 2 AGe 2 O 7 (A = Mg, Zn) with low permittivity were prepared by a solid-state reaction method. The crystal structure and microstructure of the ceramics were characterized by X-ray diffraction, transmission electron microscopy , Raman spectroscopy , and scanning electron microscopy. Both ceramics crystallized in a single melilite structure with a tetragonal space group P-42 m (113) and exhibited homogeneous microstructures. Optimum microwave dielectric properties with relative permittivity ( ε r ) of 8.56, quality factor ( Q × f ) of 28,800 GHz, and temperature coefficient of resonance frequency ( τ f ) of −70.5 ppm/°C were obtained in Sr 2 MgGe 2 O 7 sintered at 1330 °C. Sr 2 ZnGe 2 O 7 possessed ε r of 8.81, Q × f of 35,700 GHz, and τ f of −84.4 ppm/°C when sintered at 1290 °C. Thermal stability of resonance frequency was accessible when the negative τ f values of Sr 2 AGe 2 O 7 were adjusted after the formation of composite ceramics with CaTiO 3 .
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