JOURNAL OF SOLID STATE CHEMISTRY
·
2021
·
IF 3.498
Li Zeng,Tongjiang Peng,Hongjuan Sun,Jingjie Yang,Yao Li,Yating Qin
A series of Fe-doped LaNi 1-x Fe x O 3 perovskite oxide photocatalytic materials was prepared using a sol-gel method. The phase composition and morphology of LaNi 1-x Fe x O 3 samples were characterized via X-ray diffraction, scanning electron microscopy, transmission electron microscopy , X-ray photoelectron spectroscopy, and other analytical methods. The photocatalytic performance of the samples was tested by assessing the degradation rate of methyl orange. According to the results, Fe-doping caused the lattice distortion of the initially cubic of LaNiO 3 to a rhombohedral crystal system . In turn, partial substitution of Ni with Fe was found to increase the amount of oxygen vacancies , resulting in the higher mobility of lattice oxygen and thus improving the photocatalytic activity . The best photocatalytic performance was found in a LaNi 0.95 Fe 0.05 O 3 sample with a 5% Fe dopant concentration. Furthermore, the degradation rate of methyl orange in LaNi 0.95 Fe 0.05 O 3 within 120 min of visible light irradiation was as high as 98.89%, and its good degradation effect even with respect to other organic dyes such as methylene blue and rhodamine B. Finally, LaNi 0.95 Fe 0.05 O 3 was shown to maintain high photocatalytic activity and excellent recyclability even after numerous operation cycles.
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Journal of Environmental Chemical Engineering
·
2023
·
IF 7.7
Zhenxing Liu,Zhan Hu,Faxiong Li,Xinting Lai,Yuan Zhou,Jiaqi Song,Zhihui Yang,Cong Peng,Fenghua Ding,Junfang Nan,Yexin Zhang,Yanjie Liang
Icosahedral boron arsenide B 12 As 2 is a self-healing semiconductor potentially applied in harshly irradiated environments. However, doping effects were rarely investigated to expand their applications. Hereby, a low-cost mechanochemical strategy is proposed to synthesize B 12 As 2 nanocrystals with a boron transformation rate of ∼70%. Nano-B 12 As 2 of 40–50 nm could be self-doped with Fe element and purified by aqua regia. Fe accounts from ∼0.00–1.77 at% with rotational speeds. Based on nano-size effects and Fe-doping effects, the photoluminescence process shows an indirect band-gap at E g = 2.81 eV and the presence of impurity energy level at E′= 2.11 eV. The optical absorption is red-shifted from the reported UV region to the visible region. The multiply increased photocatalytic hydrogen production (249 μmol∙h −1 ∙g −1 vs. 92.2 μmol∙h −1 ∙g −1 ) and photocurrent density (∼6 times) indicate that Fe-doping enhances the photo-excitement and the separation of the photoinduced carrier. First-principles calculations reveal a robust B 12 As 2 structure doped by Fe, bonding to icosahedral B 12 clusters and its nearest As via the Fe(III) style. Doped-Fe alters HOMO and LUMO orbital components, reduces the optical band-gap and becomes the activated carrier-separation center. Overall, a novel synthetic method and mechanism of Fe-doping are revealed that would facilitate optical applications of B 12 As 2 crystals under extreme conditions.
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高影响因子
CERAMICS INTERNATIONAL
·
2018
·
IF 3.057
Jiangbo Shi,Guiqiu Chen,Guangming Zeng,Anwei Chen,Kai He,Zhenzhen Huang,Liang Hu,Jingwen Zeng,Jing Wu,Weiwei Liu
In this study, graphene wrapped Fe-doped TiO 2 (G-TiO 2 -Fe) spheres were prepared through a simple hydrothermal process. The structural, optical and photocatalytic properties of synthesized composite were characterized by field emission scanning electron microscope (FE-SEM), X-ray diffraction ( XRD), Raman Microprobe (Raman), X-ray photoelectron spectroscopy (XPS) and UV–Vis diffuse reflectance spectrophotometer (DRS). The G-TiO 2 -Fe composite showed a significant red-shift in light response edge as compared with TiO 2 . Meanwhile, the band gap exhibited an obvious decline from 3.24 to 2.99 eV. The photocatalytic capacity of G-TiO 2 -Fe was further evaluated by methylene blue (MB) degradation experiments, and the results indicated that the optimized G-TiO 2 -Fe exhibited a remarkable increase in photocatalytic activity. The superior photocatalytic performance of the novel material could be ascribed to the synthetic effects of doped Fe and wrapped graphene shells. The unique geometrical configuration and constructive component which modified the TiO 2 electronic structure will largely improve the electron transporting efficiency and restrain the electron-hole recombination.
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Journal of Energy Storage
·
2025
·
IF 9.8
Chenglin Wei,Mengdi Sun,Baoguo Zhang,Zhangyong Yan,Zihao Dang,Yongkang Xu,Lin Wu,Ya Hu
Benefiting from the low cost and natural abundance of sulfur, as well as its excellent theoretical performance metrics - including a capacity of 1675 mAh g −1 and an energy density of 2600 Wh kg −1 - lithium-sulfur (Li-S) batteries have attracted considerable attention for next-generation energy storage. However, their practical deployment is severely hindered by the intrinsic shuttle effect of lithium polysulfides (LiPSs), which leads to the loss of active materials and poor cycling stability. In this work, we report a facile hydrothermal-calcination strategy to synthesize porous nanosheet-structured Fe-doped nickel oxide (Fe-NiO) as a functional separator modifier for Li-S batteries. The polar nature of NiO enables strong chemical interactions with LiPSs, effectively anchoring polysulfides on the cathode side and suppressing the shuttle effect. Furthermore, Fe doping significantly increases the density of surface active sites, thereby enhancing the adsorption and catalytic conversion of LiPSs into insoluble Li 2 S 2 /Li 2 S species, which promotes redox kinetics and mitigates capacity fading. When applied to Li-S cells, the Fe-NiO-modified separator markedly improves the electrochemical performance, delivering a high reversible capacity of 1150 mAh g −1 at 0.2C, an excellent rate capability of 505 mAh g −1 at 5C, and outstanding long-term stability with a minimal capacity decay of 0.091 % per cycle over 500 cycles at 1C. This study presents a simple and scalable strategy for separator engineering, providing a promising pathway toward high-performance Li-S batteries.
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高影响因子
LANGMUIR
·
2025
·
IF 3.9
Yingjin Ma,Qifeng Li,Xueqing Qiu,Zhixian Li
Single-atom nanozymes can accurately mimic the catalytic centers of enzymes at the atomic scale, showing high catalytic efficiency and selectivity. Inspired by the active center of natural laccase, we constructed a nitrogen-doped carbon-based single-atom nanozyme (Fe-NC) featuring planar Fe–N4 active sites using a zeolitic imidazolate framework (Fe/ZIF-8) as a precursor. The resulting Fe–NC showed high laccase-like activity toward phenolic substrates such as 2,4-dichlorophenol, with a catalytic efficiency 77 times higher than that of natural laccase. Furthermore, Fe–NC efficiently catalyzed the degradation of tetracycline hydrochloride (77.14%) under mild conditions, with an activity 13 times that of laccase. It also selectively and oxidatively depolymerized birch lignin into valuable aromatic monomers, including vanillin and vanillic acid. These findings highlight the key role of planar Fe–N4 coordination in improving bioinspired catalysis and reveal the great potential of single-atom nanozymes in biomass valorization.
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PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2016
·
IF 3.299
Lingjun Bu,Zhou Shi,Shiqing Zhou
In this paper, a mathematical model on Fe(II)-activated persulfate oxidation of atrazine (ATZ) was tested using the rate constants from literature, and the degradation kinetics and mechanism of ATZ degradation in Fe(II)/persulfate (Fe 2+ /PS) system were investigated to verify the model. Some influence factors were taken into consideration in this model, including molar ratio of Fe 2+ and PS, initial ATZ concentration, natural organic matter (NOM) concentration, tertiary butanol (TBA) and methanol (MeOH) concentrations. Corresponding experimental data could be predicted accurately according to this model. Both experimental data and predicted results implied that a molar ratio of Fe 2+ and PS at 1:1, low initial ATZ and NOM concentrations were favorable for ATZ degradation. Besides, the radical species were determined via evaluating the effect of TBA and MeOH, and results confirmed that both sulfate radical (SO 4 − ) and hydroxyl radical (OH ) existed in this system. To investigate the predominant radical in Fe 2+ /PS system, nitrobenzene (NB) was used as a probe compound which only react with OH . According to the degradation efficiency of NB and ATZ in Fe 2+ /PS system, it could be concluded that only small amount of OH were produced and SO 4 − made a major contribution to ATZ degradation in Fe 2+ /PS system. Experimental data, as well as the mathematical model in this study, improved our understanding on the effect of operating parameters for ATZ degradation in Fe(II)-based advanced oxidation processes.
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高影响因子
Materials Today Bio
·
2025
·
IF 10.2
Hongping Wan,Zhengqun Huang,Mingrun Tang,Huirong Tan,Kai Deng,Yingnan Liu,Xinghong Zhao,Hongjun Chen
Enveloped viruses such as coronaviruses are highly transmissible, necessitating effective prevention and inactivation strategies. In this study, we engineered uniform, small-sized (∼57 nm) iron-phenolic nano-networks (NA-Fe) that exhibit high lipoxidase-like activity for the inactivation of enveloped virus, encompassing both DNA virus (Pseudorabies, PRV) and RNA virus (Transmissible Gastroenteritis, TGEV; and Porcine epidemic diarrhea virus, PEDV). Theoretical studies indicate that NA-Fe facilitates the adsorption of pentadiene moieties within the viral envelope through interactions between the d -orbital electrons of iron and the π-electrons of pentadiene. This interaction leads to activation of the C=C bonds, potentially resulting in disruption of the viral envelope. Besides its extracellular antiviral effects, NA-Fe also suppresses intracellular viral replication by stimulating antiviral innate immune responses, and upregulate the expression of interferon-stimulating genes (ISGs). In vivo studies demonstrate that NA-Fe exhibits favorable biosafety, and intranasal administration significantly reduces viral titers while providing effective antiviral protection in PRV-infected mice. Notably, surfaces coated with NA-Fe, such as fences and air purifiers in farm facilities, provide effective antiviral protection. Collectively, these findings demonstrate that NA-Fe exhibits potent broad-spectrum antiviral activity against both extracellular and intracellular viruses, highlighting its potential for application in comprehensive biosecurity and infectious disease control.
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DOI
PubMed
高影响因子
RSC Advances
·
2014
·Vol. 5
·期 10
·7253-7259
·
IF 3.708
Yuanlong Xiao,Xiangyu Guo,Hongliang Huang,Qingyuan Yang,Aisheng Huang,Chongli Zhong
A cheap and biocompatible metal–organic framework MIL-88B(Fe) (MIL = Material Institut Lavoisier) was synthesized and incorporated into Matrimid® 5218 to fabricate mixed-matrix membranes (MMMs) for gas separation. Separation performances of the MIL-88B(Fe)/Matrimid MMMs were tested for the single gas permeation of H2 and CH4 as well as the mixture gas separation of an equimolar binary H2–CH4 mixture. Due to the molecular sieving effect, the incorporation of MIL-88B(Fe) can enhance H2 permeability but hinder the transport of CH4 in MIL-88B(Fe)/Matrimid MMMs, thus resulting in enhanced separation selectivity of H2–CH4. At 298 K and ΔP = 3.0 bar, compared with those of a pure polymeric membrane, the H2 permeability and H2–CH4 mixture separation factor of MMMs with a MIL-88B(Fe) loading of 10% increased by 16% and 66%, respectively. In addition, the operation temperature has a significantly positive effect on the separation of a H2–CH4 mixture.
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高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2021
·
IF 8.128
Hongda Li,Honggao Deng,Shaonan Gu,Chenpu Li,Boran Tao,Shumin Chen,Xiong He,Guofu Wang,Wenfeng Zhang,Haixin Chang
The “FeMo cofactors” in biological nitrogenase play a decisive role in nitrogen reduction. Herein, a novel bionic Fe/Mo bimetallene was applied in photocatalytic nitrogen reduction. The surface coating Fe/Mo bimetallene of Bi 2 Mo 0.3 W 0.7 O 6 (BMWO) nanocrystals could effectively promote the separation and transportation of photogenerated carriers by multi–electron redox reactions and deliver 2.8 times longer photo–carrier lifetime. Consequently, the nitrogen fixation activity of Fe/Mo bimetallene–coated BMWO nanocrystal photocatalyst was obviously enhanced (218.93 μmol g –1 h −1 ), which was about 4.8 times that of unmodified BMWO nanocrystals. This work provides a novel approach to design bionic Fe/Mo bimetallene–modified inorganic semiconductor photocatalysts for nitrogen reduction.
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高影响因子
JOURNAL OF STRUCTURAL CHEMISTRY
·
2022
·Vol. 63
·期 4
·634-641
·
IF 1.004
Wu G. L.,Zheng C. Y.
Abstract [Fe III (OMe)(Hedtb)](ClO 4 ) 3 ·6.5CH 3 OH ( 1 ) and [Fe III (O n- Bu)(Hedtb)](ClO 4 ) 3 ·3 n -BuOH ( 2 ) (edtb = N,N,N′,N′-tetrakis[(2-benzimidazolyl)methyl]-1,2-ethanediamine) were prepared and display lipoxygenase activity. X-ray crystallography reveals that the Fe III centers in complexes 1 and 2 are ligated to three nitrogens of benzimidazole and two alkylamine nitrogen atoms from the edtb ligand, with a terminal alkyoxyl group occupying the sixth position. Complexes 1 and 2 both possess a Fe III –O R center ( R = Me, 1 ; n -Bu, 2 ) with Fe–O bond distances of 1.799(3) Å and 1.789(5) Å, respectively. The UV-Vis spectra and electrochemical properties of the complexes were recorded. Both complexes have strong absorption peaks at around 375 nm and display lipoxygenase activity.
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高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2022
·
IF 4.598
Ping Xiao,Guodong Zhu,Xiaohong Shang,Bin Hu,Boshuang Zhang,Zhaoyu Tang,Jianmao Yang,Jianyun Liu
The Fe-metal organic framework decorated MXene (Fe-MOF/MXene) was in-situ synthesized by one-step hydrothermal method in the presence of MXene. Using Fe-MOF/MXene as modifier, the obtained Fe-MOF/MXene electrode presented excellent electrochemical activity due to the high surface area and good conductivity of MXene. A sensitive arsenite electrochemical sensor was fabricated based on the strong As-hydroxyl bonding at the Fe-MOF/MXene electrode, confirmed by X-ray photoelectron spectroscopy. Cyclic voltammetry characterization indicated that MXene facilitated the charge transfer with enhanced electrochemical response. The Fe-MOF/MXene modified electrode exhibited super-high current response to As(III) by square wave anodic stripping voltammetry, with extremely high sensitivity (8.94 µA·(ng·L −1 ) −1 ·cm −2 ) and super-low limit of detection (0.58 ng·L −1 ). The analysis of the real water demonstrated that the Fe-MOF/MXene-based sensor was feasible for the detection of As(III) in practical application.
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高影响因子
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
·
2025
·
IF 4.7
Yanhao Xu,Ziyi Zhong,Pinle Zhang,Huancheng Huang,Kuan Cai,Xinliang Liu
Persistent organic pollutants (POPs) represent a significant environmental and health risk due to their high toxicity, persistence, strong accumulation potential, and adverse effects on human health. 4-Chlorophenol (4-CP), a type of POP, has low catalytic efficiency at low concentrations and is easily interfered with by other pollutants, making its degradation challenging. A new “recognition-enrichment-in-situ degradation” strategy is introduced to selectively remove chlorophenols from contaminated aqueous environments. In this study, ionic liquids were incorporated into the UIO-66 framework as active sites for selective adsorption. 4-CP contains phenolic hydroxyl groups and exhibits high polarity. The dispersive interactions between 4-CP and ionic liquids, along with hydrogen-bonding interactions between the Tf 2 N anion and the hydroxyl groups of 4-CP, enhance the selective enrichment of 4-CP within the nanocavities of the metal–organic frameworks (MOFs). Fe 3+ was then introduced, enabling in-situ degradation of 4-CP through photo-induced generation of free radicals and cavities from H 2 O 2 catalyzed by Fe-IL@UIO-66. The results indicated that the adsorption capacity of IL@UIO-66 for 4-CP reached 53 %, significantly higher than that for five other organic pollutants. The adsorption capacity of IL@UIO-66 for 4-CP reached 509.5 mg g −1 , 49.9 % greater than that of the original UIO-66. The degradation efficiency of 4-CP by Fe-IL@UIO-66 increased from 61 % to 81 %, and after four cycles, the material retained a catalytic activity with a degradation efficiency of 64.2 %. This study provides valuable insights into the recognition-enrichment-in-situ catalytic strategy for treating low-concentration, highly toxic wastewater.
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高影响因子
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