Journal of Inorganic and Organometallic Polymers and Materials
·
2013
·Vol. 23
·期 6
·1534-1539
·
IF 1.174
Yan Bianling,Zhou Xiaojun,Li Yuanyuan,Yin Fei,Zou Yang,Jiang Yinzhi,Wang Xing,Xie Jingli
A novel 3d–4f heterometallic coordination complex [Ce(H 2 O) 6 (CuL) 2 ]·NO 2 ·7H 2 O ( 1 ) (H 3 L = glycylglycine, N -[1-(2-hydroxy, phenyl)-propylidene]) was synthesized and characterized by IR, elemental analysis, TGA and single crystal X-ray diffraction. An octameric water cluster consisting of a planar tetrameric water ring and four dangling water molecules were observed in 1 . Variable-temperature magnetic data shows antiferromagnetic behavior for 1 .
研究领域:
化学
·
材料科学
✓ 已验证
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2022
·
IF 9.965
Kunli Song,Shuqi Zhao,Zhenguo Li,Kaixiang Li,Yurong Xu,Yijun Zhang,Yonghong Cheng,Jian-Wen Shi
SSZ-13 has been commercialized as a catalyst in diesel engines for the selectivity catalytic reduction of nitrogen oxides (NO x ) with ammonia (NH 3 -SCR), but the catalyst is facing the problem of poisoning. Herein, two well-designed catalysts, Cu-SSZ-13 and cerium (Ce) doped Cu-SSZ-13 are synthesized, and their tolerance to zinc (Zn) and phosphorus (P) poisoning alone and together are explored in detail. The research found that Zn and P poisoning alone leads to the destruction of Cu-SSZ-13 structure, resulting in the decline of denitration (de-NO x ) performance following the mechanism dominated by Eley-Rideal (E-R). Surprisingly, it is found that zinc phosphate particles are formed at inactive sites on the surface of Cu-SSZ-13 in the presence of Zn and P together, which protects the active sites, enhances the adsorption of nitric oxide. As a result, the excellent de-NO x performance of Cu-SSZ-13 is well maintained following the dual mechanism of E-R and Langmuir-Hinshelwood (L-H). In addition, the introduction of Ce stabilizes the active sites, so as to improve the de-NO x performance and the poisoning tolerance of Cu-SSZ-13. This work deeply analyzes the reasons of Zn and P poisoning and the positive effect of Ce on Cu-SSZ-13, which provides ideas for improving the poisoning tolerance of Cu-SSZ-13 and promotes the further application.
研究领域:
环境科学
·
催化化学
✓ 已验证
DOI
PubMed
高影响因子
KOREAN JOURNAL OF CHEMICAL ENGINEERING
·
2017
·Vol. 34
·期 12
·3132-3141
·
IF 2.007
Zhang Wei,Li Xin,Wang Hong,Song Yongji,Zhang Shenghong,Li Cuiqing
Deep desulfurization of model oil by photocatalytic air oxidation and adsorption using Ti (1− x ) M
x
O 2 (M=Zr, Ce) was investigated. Ti (1− x ) M
x
O 2 (M=Zr, Ce) was prepared by urea gelation/co-precipitation method, and characterized by N 2 adsorption, XRD and UV-vis spectra. UV irradiation greatly enhanced the adsorptive capacity and selectivity of TiO 2 -ZrO 2 for organosulfur in model oil because organosulfur compounds were first photocatalytically oxidized to sulfoxides and sulfones over TiO 2 -ZrO 2 , which were then selectively adsorbed on the bifunctional material due to much higher polarities of generated sulfoxides and sulfones. The Ti/Zr molar ratio and calcination temperature were optimized to 5 : 5 and 500 °C with the sulfur removal of 99.6% after reaction for 2 h under UV irradiation. After adding 25 wt% toluene into model oil, the sulfur removal could still reach 97.2% after reaction for 7 h. TiO 2 -ZrO 2 could be well regenrated by washing with acetonitrile followed by thermal treatment in air.
研究领域:
化学工程
·
环境科学
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2026
·
IF 6.3
Haicheng Liu,Wenhao Zhang,Chuang Zhang,Shuwen Wang
The rapid recombination of photogenerated charge carriers is a major challenge for photocatalysts. In this study, a novel Z-scheme heterojunction photocatalyst was synthesized via a hydrothermal method by coupling bimetallic Ce/Zr-NH 2 -UiO-66 (CNU) with solid solution of BiOCl 0.7 I 0.3 (Bi-0.3) for ciprofloxacin (CIP) degradation. The catalyst combines the excellent charge separation ability of Ce/Zr bimetallic metal organic framework (MOF) with the broad light absorption of solid solution of bismuth oxyhalide, achieving outstanding photocatalytic performance under visible light. The characterization results demonstrate that the formation of the Z-scheme heterojunction significantly enhances the material's visible light absorption and promotes efficient electron-hole separation through the built-in electric field, thereby effectively suppressing the recombination of photogenerated charge carriers. Photoelectrochemical and radical trapping experiments further demonstrated excellent interfacial charge transfer and reactivity. The catalyst achieved a CIP removal efficiency of 90.06 ± 2.78 % within 90 min and exhibited good stability in various water matrices. The response surface methodology analyzed the interactions between key reaction parameters, while density functional theory (DFT) confirmed that the electron transfer mechanism follows a Z-scheme heterojunction. It also predicted the degradation pathway of CIP and identified the primary attack sites, along with evaluating the environmental toxicity of the intermediate products. This study provided new insights into the design of bimetallic MOF-based Z-scheme heterojunction and expands the application potential of photocatalysts for environmental remediation.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2019
·
IF 4.175
Chaocheng Liu,Xucai Kan,Feng Hu,Xiansong Liu,Shuangjiu Feng,Jiyu Hu,Wei Wang,Khalid Mehmood Ur Rehman,Mudssir Shezad,Cong Zhang,Haohao Li,Shengqiang Zhou,Qiuyue Wu
Herein, we have systematically illustrated the specific impact of Ce-Zn co-substituted M-type strontium hexaferrites on its microstructure and magnetic properties . An evident phase pattern change process and performance improvement are observed from a series of systematic measurements. The results of X-ray diffraction show that the single phase can be obtained when x = 0.00–0.30, the other unexpected diffraction peaks of hematite ( α -Fe 2 O 3 ) will appear in the patterns as x > 0.3. Scanning electron microscopy exhibits that all samples formed the uniform plane hexagonal structures with different substitution contents. FT-IR spectra verify the confirmation that M-type hexagonal structure has been formed thoroughly. M ( T ) curve displays the ferrimagnetic behavior of temperature dependent magnetization. And vibrating sample magnetometer indicates both M s and H c can be improved significantly, indicating an excellent performance in novel recording devices.
研究领域:
材料科学
·
磁学
·
陶瓷学
·
固态化学
✓ 已验证
DOI
高影响因子
Catalysts
·
2024
·Vol. 14
·期 11
·752
·
IF 3.8
Mengjie Lu,Run Cheng,Li Wang,Dandan Liang,Meng Qin,Bili Wang,Rui Song,Duo Chen
The elaborate design of inexpensive, high-performance electrocatalysts from earth-abundant elements toward oxygen evolution reaction (OER) is critical in various (electro)chemical processes. Herein, a novel binder-free catalyst of Ce-coupled Ni3S2/NiS supported on Ni foam (Ce-Ni3S2/NiS@NF) is successfully synthesized via a facile one-step hydrothermal method that enables practical feasibility with a significant enhancement of OER activity through anchoring Ce dopants on an Ni3S2/NiS nanobud host. Ce species coupling can modulate electronic structure, which reduces the reaction energy barrier and optimizes OER catalytic activity. More profoundly, the superhydrophilic and superaerophobic properties of the Ce-Ni3S2/NiS@NF electrode further promote mass transfer. As a result, the Ce-Ni3S2/NiS@NF electrode exhibits excellent OER activity with a low overpotential of 236 and 350 mV to achieve current densities of 10 and 100 mA cm−2, respectively, and long-term durability for 24 h in alkaline medium. These results could supply valuable guidelines for the design of other OER catalysts and beyond.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2020
·
IF 3.807
Kewei Jiang,Yawei Shao,Valeri Smolenski,Alena Novoselova,Qi Liu,Minghui Xu,Yongde Yan,Jing Yu,Milin Zhang,Jun Wang
The electrode reactions of the Ce 3+ /Ce couple in molten LiCl–KCl eutectic in the temperature range 723–823 K on solid Mo electrodes were investigated by electrochemical techniques . The mechanism of deposition of metallic cerium has been established. It was found that the cathode reaction is irreversible and proceeds in one stage. The apparent standard Gibbs energy of CeCl 3 formation from the elements was calculated. The values of enthalpy and entropy were equal: ΔH* = − 1000.2 kJ/mol, ΔS* = 166.0 J/mol·K. The conditions of high-purity cerium production have been studied. The chemical structure of cathode deposits as well as the surfaces of the crucible were investigated by XRD , ICP and SEM-EDS methods. It was established that the best results for purification of the cathode product from impurities were achieved in the range 40–60 mA/cm 2 using a two-stage electrolysis. The amounts of the main impurities in the final product were 0.005 wt% Al, 0.0021 wt% Fe, and 0.003 wt% Si. The total purity of metallic cerium after cleaning was increased up to 99.971 wt% if a vitreous carbon crucible was used.
研究领域:
冶金学
·
电化学
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2026
·
IF 6.7
Heng Dai,Qi Yu,Zhanyu Cao,Jiaxin Wang,Wenbo Sun,Jiayu Wang
Developing lightweight microwave-absorbing materials with a low filler loading, strong attenuation capability, and broad effective absorption bandwidth is an important requirement in electromagnetic protection and radar stealth. In this work, a nitrogen-doped reduced graphene oxide/Ce-doped strontium ferrite@nitrogen-doped carbon (NRGO/Ce-SrM@NC) heterointerfacial absorbing structure was constructed by hydrothermal assembly and dopamine-derived carbonization. In this system, Ce-SrM provides the magnetic response, NRGO builds a lightweight conductive network, and the NC shell acts as an interfacial bridging layer to regulate the coupling between magnetic particles and graphene sheets. Structural characterization shows abundant defect sites and close particle-sheet contact interfaces. At a filler loading of only 5 wt%, the NRGO/Ce-SrM@NC composite achieves a minimum reflection loss (RL min ) of −53.2 dB at a matching thickness of 2.6 mm and a maximum effective absorption bandwidth (EAB) of 7.22 GHz. Its excellent electromagnetic wave absorption (EWA) performance mainly originates from the synergistic effect of balanced impedance matching, conductive loss, dipole polarization, interfacial polarization, magnetic resonance, and multiple scattering. Further CST simulations show that a PEC plate coated with the NRGO/Ce-SrM@NC composite can achieve a radar cross section reduction of 41.35 dB cm⁻¹ . Meanwhile, the simulated moth-eye-inspired gradient structure based on the NRGO/Ce-SrM@NC composite extends the EAB to cover the entire 2–18 GHz range. This study provides a feasible strategy for the design of low-filler, broadband electromagnetic wave-absorbing materials and radar stealth structures.
✓ 已验证
产品关联
DOI
高影响因子
ANALYTICA CHIMICA ACTA
·
2026
·
IF 6.1
Nanke Ma,Anqi Wei,Huiling Peng,Lixia Xie,Yuan Jin,Zhengzhi Yin,Guangli Li
Background Chirality plays a critical role in drug efficacy and environmental safety. The antibacterial activity of ofloxacin resides almost exclusively in its S-enantiomer (levofloxacin, LEV), while the R-enantiomer contributes little to therapeutic effects but may pose unnecessary risks. Rapid and reliable methods for enantioselective determination of ofloxacin enantiomers are therefore essential for pharmaceutical quality control, food safety monitoring, and environmental analysis. However, existing electrochemical sensors often suffer from limited enantioselectivity and insufficient sensitivity. To address this challenge, a novel enantioselective electrochemical platform is developed. Results A β-cyclodextrin/cerium-doped copper metal-organic framework/carboxylated multi-walled carbon nanotube composite (β-CD/Ce-doped Cu-MOF/MWCNTs-COOH) was fabricated on a glassy carbon electrode. The sensor achieves discrimination of ofloxacin enantiomers with an I L /I D ratio of 3.39. DFT calculations at pH 4.0 reveal that β-CD binds LEV with higher adsorption energy (−63.8 kJ/mol) than DEX (−58.3 kJ/mol), confirming the superior response for LEV originates from stereospecific inclusion. Quantitative analysis of LEV shows two linear ranges (0.03–1 μM and 1–10 μM) with a low detection limit of 0.01 μM. The sensor also enables accurate determination of LEV percentage in enantiomer mixtures across 0–100%. Excellent selectivity against common interferents, good reproducibility (RSD = 0.98%), repeatability (RSD = 1.26%), and long-term stability (95.2% retention after 21 days) are demonstrated. Practical applicability is validated by detecting LEV in commercial eye drops, honey, and tap water with satisfactory recoveries (96.0–108.0%). Significance and novelty This work presents the first application of Ce-doped Cu-MOF/β-CD/MWCNTs-COOH composites for the enantioselective electrochemical sensing of ofloxacin, a chiral fluoroquinolone antibiotic. The synergistic combination of high conductivity, abundant catalytic sites, and stereospecific host-guest recognition provides a generalizable strategy for high-performance enantioselective sensing, with promising applications in pharmaceutical, food, and environmental analysis.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2026
·
IF 4.6
Cheng Xiong,Liyin Bu,Xue Bai,Yongzhong Fu,Quan Wang
Cts/Ce-UiO-66 was developed for sensitive ratiometric detection of Hg 2+ . • Intrinsic Ce 4+ /Ce 3+ redox couple in MOF provides a stable reference signal. • Chitosan coating promotes Hg 2+ enrichment and stabilizes the modified film. • The sensor showed a 3.73 nM LOD and 95.0%–105.3% recovery in pond water. Mercury pollution remains a serious environmental concern because of its toxicity, persistence, and bioaccumulation in aquatic environments. Herein, a ratiometric electrochemical sensor for Hg 2+ detection was developed using a chitosan/Ce-UiO-66 (Cts/Ce-UiO-66) composite. Ce-UiO-66 was used as a redox-active sensing scaffold. Its porous framework may provide accessible interfacial sites that may contribute to Hg 2+ accumulation, while the intrinsic Ce 4+ /Ce 3+ redox response provides a built-in electrochemical signal for internal normalization under controlled measurement conditions. Chitosan was introduced as a film-forming matrix. The amino and hydroxyl groups of chitosan may contribute to Hg 2+ interfacial preconcentration, while the polymer matrix improves the stability of the modified film. The integration of the proposed Cts-assisted Hg 2+ interfacial accumulation and the intrinsic Ce-related normalization signal enabled ratiometric Hg 2+ quantification. Under optimized differential pulse voltammetry conditions, the sensor exhibited a linear response toward Hg 2+ over the concentration range of 0.10–3.00 μM, with a limit of detection of 3.73 nM. The sensor was further evaluated in a fish-pond water sample, achieving recoveries of 95.00–105.33% at the tested spiking levels. These results support the preliminary feasibility of the Cts/Ce-UiO-66-based ratiometric sensor for Hg 2+ determination in the tested fish-pond water matrix under the present experimental conditions. Scheme 1. Schematic illustration of the preparation and sensing processes of Cts/Ce-UiO-66/GCE. Download: Download high-res image (108KB) Download: Download full-size image
✓ 已验证
DOI
高影响因子
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
·
2026
·
IF 7.1
Yong-hong Niu,Yuan Tian,Lifei Yang
Hydrogen-rich syngas was produced from co-gasification of CS and CG. • 4Ce-8Ni/C-CaO markedly enhanced H 2 formation and syngas quality. • The maximum H 2 content reached 59.71 mol%. • Ce promoted Ni dispersion, oxygen vacancy formation, and coke resistance. The catalytic co-gasification of agricultural residues and coal-derived solid wastes offers an industrially promising route for converting low-value carbon resources into hydrogen-rich syngas. In this study, a Ce-Ni/C-CaO composite catalyst was prepared by impregnation and applied to the steam-assisted co-gasification of corn stover (CS) and coal gangue (CG) in a two-stage fixed-bed system. The effects of metal loading, feedstock ratio, temperature, and steam flow rate were investigated, the structure-performance relationship of the catalyst was further examined using XRD, SEM/BET, TEM/STEM-EDS, XPS, H 2 -TPR and O 2 -TG analyses. Under the optimal conditions of CS:CG = 5:5, pyrolysis at 850 ℃, reforming at 900 ℃, and a steam flow rate of 1 mL/min, the 4Ce/8Ni-C/CaO catalyst achieved an H 2 content of 59.71 mol% and a total gas yield of 19.13 mmol/g and an H 2 /CO ratio of 5.22. Characterization results indicated that the Ce species regulated the distribution of surface oxygen species, enhanced oxygen mobility, promoted the Ce 4+ /Ce 3+ redox cycle, and influenced the evolution of catalyst pore structure during the reaction. Download: Download high-res image (221KB) Download: Download full-size image
✓ 已验证
DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2026
·
IF 5.2
Haiyan Wu,Jianlei Wu,Nian Huang,Jean-François Masson,Haifeng Zhou,Wenjuan Zhou,Wei Lin,Guobin Liang
A sensitive ratiometric electrochemical strategy for MMC detection is developed. • Polythionine serves as an internal reference for improved response stability. • Ce-Ni-MOF/MWCNTs enhance interfacial electron transfer. • Molecular imprinting enables selective MMC recognition. • MMC detection is validated by UPLC-QTOF-MS in water samples. Mitomycin C (MMC) is a widely used antitumor antibiotic, and its rapid and selective detection is crucial for monitoring its occurrence in environmental water samples. In this work, a ratiometric electrochemical sensor was constructed by sequential modification of a bimetallic Ce-Ni-metal-organic framework (Ce-Ni-MOF)/multi-walled carbon nanotube (MWCNTs) composite, polythionine (pThi) and a molecularly imprinted polymer (MIP) on a glassy carbon electrode. The Ce-Ni-MOF/MWCNTs composite facilitated electron transfer, contributing to the enhanced sensitivity of the sensing platform. The pThi was electropolymerized onto the modified electrode surface to provide an internal reference signal, while the ratiometric response was achieved through two electrochemical channels, with the [Fe(CN)₆] 3−/4 − redox probe serving as the response signal and the pThi signal as the reference, enabling effective correction of measurement variations. Under optimized conditions, the sensor exhibited a linear response to MMC over the concentration range of 0.1–100 nM, with a low detection limit of 0.046 nM and a limit of quantification of 0.075 nM. Owing to the specific molecular recognition of the MIP layer and the internal reference function of pThi, the proposed sensor demonstrated satisfactory selectivity, repeatability, reproducibility and stability. Furthermore, the sensor was successfully applied to the determination of MMC in water samples, achieving recoveries of 87–112%. The analytical performance of the proposed sensor was further validated by comparison with the results obtained using ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS). This work presents a reliable and sensitive ratiometric electrochemical sensing strategy and demonstrates its feasibility through a proof-of-concept study for MMC detection in environmental water samples. Download: Download high-res image (304KB) Download: Download full-size image
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）