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Nano-Micro Letters · 2025 ·Vol. 17 ·期 1 ·1-14 · IF 36.3

Specific Sn–O–Fe Active Sites from Atomically Sn-Doping Porous Fe2O3 for Ultrasensitive NO2 Detection

Zhong Yihong,Yuan Guotao,Bao Dequan,Tao Yi,Gao Zhenqiu,Zhao Wei,Li Shuo,Yang Yuting,Zhang Pingping,Zhang Hao,Sun Xuhui

The heteroatom atomically doping strategy was reported to construct highly efficient sites on metal oxides for the detection of low-concentration gas. The atomically dispersed Sn atoms were intentionally incorporated into the Fe 2 O 3 lattice during the oxidative annealing of Fe-based metal organic framework, leading to specific Sn–O–Fe sites, porous structures, and abundant oxygen vacancies. The optimized Sn-Fe 2 O 3 exhibited exceptional sensing performance for NO 2 detection: ultra-high sensitivity ( Rg / Ra =2646.6 to 1 ppm NO 2 ), ultra-low limit of detection (10 ppb), and high selectivity.

研究领域: 材料科学 · 环境监测 · 化学传感器
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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Two birds with one stone: Fe-doped CuAlO2 ceramics for efficient microwave absorption and high emissivity

Jinbu Su,Chenyi Shi,Chenzhuo Gong,Yuyi Xu,Yunong Xie,Xuli Lin,Xinyu Dong,Weixin Du,Yuchang Qing,Fa Luo

Semiconductor oxides are ideal candidates for future electromagnetic wave absorption and thermal management due to their hole-conducting properties. However, in practical applications, due to its limited conductivity, its development and application in the field of electromagnetic wave absorption and thermal management are greatly limited. The CuAl 1-x Fe x O 2 ceramics were synthesized using the high-temperature solid-phase method to study their microwave absorption and infrared emissivity characteristics. The introduction of Fe significantly improves the electromagnetic wave absorption and emissivity characteristics of CuAlO 2 ceramics. The effects of Fe doping on the dielectric constant, permeability, microstructure, and surface morphology of the composite were systematically analyzed. The results show that Fe doping leads to lattice distortion and the introduction of defects, which effectively improves the conductivity and polarization loss of the material, thus enhancing the dielectric loss and magnetic loss mechanisms of the material and obtaining excellent microwave absorption performance. The results show that when the doping amount of Fe is 3 %, the minimum reflection loss RLmin can reach −50.41 dB, and the effective absorption bandwidth EAB is 4.2 GHz. When the doping amount of Fe is 9 %, the infrared emissivity reaches a peak of 0.936. The porous structure further enhances the absorption and radiation properties of CuAl 1-x Fe x O 2 ceramics. It is further indicated that CuAl 1-x Fe x O 2 ceramics have great application potential in electromagnetic wave absorption and thermal management.

CAS / MDL: 64-17-5
研究领域: 材料科学 · 电磁学
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Water Reuse · 2024 ·Vol. 14 ·期 1 ·39-50 · IF 4.3

Removal of tellurium(IV) from environmental aquatic systems using metal-organic framework material MIL-100(Fe)

Huang Yiru,Li Youyou,Zhong Qingwei,Luo Chen

View large Download slide View large Download slide Close modal Metal-organic framework (MOF) materials, characterized by their porosity and large specific surface areas, exhibit excellent adsorption properties. With the aim of removing Te(IV) from environmental aquatic systems, this study is the first to propose the use of MIL-100(Fe). The material reveals a strong adsorption capacity for Te(IV), with maximum adsorption of 531.9 mg/g, superior to other adsorbent materials. Adsorption isotherm and kinetic models indicate that the adsorption process primarily involves monolayer chemical adsorption. According to the thermodynamic parameters, the adsorption reaction is endothermic. The experiment individually examined factors affecting the material's adsorption performance, including adsorbent dose, initial concentration of Te(IV), pH, adsorption time, and coexisting ions. Even under high ion strength conditions and high concentrations of coexisting ions, the material's adsorption efficiency for Te(IV) still reached over 94%. The material has been successfully applied to remove Te(IV) from lake water, river water, and seawater, yielding satisfactory results. Due to the high salinity and ionic strength of the solution, the removal efficiency of Te(IV) in the seawater matrix was slightly lower than that in freshwater (river and lake water). Thus, this material shows promise for the removal of Te(IV) from complex aquatic systems. MIL-100(Fe) was prepared and characterized. The Te(IV) can be adsorbed by MIL-100(Fe) effectively, and the adsorption process was primarily a monolayer chemical adsorption and an endothermic reaction. The Te(IV) can be removed effectively in environmental water supplies by MIL-100(Fe).

研究领域: 环境科学 · 材料科学
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PHYSICA STATUS SOLIDI A-APPLICATIONS AND MATERIALS SCIENCE · 2024 ·Vol. 221 ·期 12 ·2300874 · IF 1.9

Fe-La-Ce-ZSM-5 Zeolite for Adsorbing Congo Red

Jie Yang,Zhengkun Cai,Dong Li

In this experiment, ZSM-5 molecular sieves are prepared by hydrothermal synthesis and modified by impregnation with Fe, La, and Ce loading. X-ray diffraction, X-ray photon-electron spectroscopy, and scanning electron microscopy show that Fe, La, and Ce elements are successfully loaded onto the surface of the material, and the surface area of Fe-La-Ce-ZSM-5 is 241.66 m 2 g −1 . A systematic study on the adsorption of Congo red solution is carried out using Fe-La-Ce-ZSM-5 molecular sieves and it is found through the adsorption data that the adsorption process is more in line with Langmuir and the proposed second-order kinetic model, and the theoretical saturated adsorption capacity is 2669.19 mg g −1 . The adsorption process is recycled four times and still has more than 60 % removal performance for high-concentration Congo red solution. The results of this experiment show that Fe-La-Ce-ZSM-5 molecular sieves show excellent removal performance for Congo red dye in wastewater.

研究领域: 环境科学 · 材料科学 · 化学工程
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

CeO2-confined Ni-Fe alloy enhanced high-temperature CO2 hydrogenation to CO

Bowen Lu,Ziqiang Han,Xinyu Zhi,Liqi Zhang

NiFe 2 O 4 exhibits excellent redox properties and is widely applied in catalytic reactions. However, rapid inactivation under reaction conditions limited its industrial applications. In this study, CeO 2 -NiFe 2 O 4 composite catalysts were synthesized, and the Reverse Water Gas Shift (RWGS) reaction was measured to reveal its CO 2 hydrogenation performance under a high-temperature condition. NiFe 2 O 4 catalysts got deactivated after being reduced to Fe-Ni alloy at 700 °C, decreasing the CO 2 conversion rate. CeO 2 addition can significantly improve its high-temperature activity, and 20CeO 2 -NiFe 2 O 4 exhibited the best catalytic activity (80.85 %, 700 °C). The CeO 2 -confined maintained Ni-Fe alloy with a relatively small crystal size and larger specific surface area, supporting more active sites for CO 2 hydrogenation. CeO 2 addition induced higher oxygen vacancy concentration, enhancing CO 2 activation and formates species formed on 20CeO 2 -NiFe 2 O 4 , resulting in higher CO 2 conversion activity. In addition, 20CeO 2 -NiFe 2 O 4 maintained its catalytic stability for 50 h at 700 °C. The CeO 2 confined enhanced the high-temperature stability of Fe-Ni alloy. CeO 2 and formed CeFeO 3 dispersed in 20CeO 2 -NiFe 2 O 4 inhibited excessive aggregation of Fe-Ni alloy, and CeO 2 inhibited carbon deposition on Fe-Ni alloy, improving Fe-Ni alloy’s reaction stability under RWGS reaction conditions. CeO 2 confined may give insight into improving metal stability under high-temperature and reductive conditions in heterogeneous catalysis.

研究领域: 催化化学 · 材料科学 · 环境科学
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LANGMUIR · 2024 · IF 3.7

Bifunctional Photothermal Evaporator Based on an MXene/Fe-MOF Collaborative Effect toward Efficient Solar Steam Generation and Simultaneous VOC Removal

Wenqing Han,Yehai Yan,Huifang Wang,Jinzhong Li,Ping Zhao,Zhihao Liu,Fei Yu,Jian Cui,Guangfa Zhang

Solar-driven interfacial water evaporation has become one of the most promising approaches to effectively harvesting freshwater, yet the fabrication of high-performance and multifunctional solar interfacial evaporators (SIEs) still remains a huge challenge to date. In this study, a multifunctional MXene and Fe-MOF@cellulose acetate/polyvinylpyrrolidone (MXM@CP) SIE was prepared via a facile “electrospinning and suction filtration deposition” coupling strategy. Thanks to the incorporation of MXene, MXM@CP displayed excellent photothermal conversion performance. Together with the fast water transport channel provided by the porous cellulose acetate electrospinning substrate, a remarkable solar-driven water evaporation property was achieved for MXM@CP, showing a higher water evaporation rate of 1.1 kg m–2 h–1 under one sun irradiation. Moreover, the resultant composite film also exhibited excellent Fenton catalytic activity to effectively degrade volatile organic compounds (VOCs) due to the synergistic effect of the MXene and Fe-based MOF (Fe-MOF). Particularly, a relatively higher degradation rate of 82.8% was acquired for the resulting evaporator toward the benzene contaminant. These results provide new insights into the construction of high-performance and multifunctional SIEs toward clean freshwater collection from the VOC-contaminated water system.

CAS / MDL: 100-21-0
研究领域: 材料科学 · 环境科学 · 能源科学
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MICROCHIMICA ACTA · 2025 ·Vol. 192 ·期 3 ·1-10 · IF 5.3

Rapid determination of malachite green in fish by surface-enhanced Raman spectroscopy combined with MIL-100 (Fe)

Han Hongyu,Huang Yiqun,Miao Junjian,Lai Keqiang

Surface-enhanced Raman spectroscopy (SERS) was combined with stoichiometric analysis to synthesize a AuNPs@MIL-100 (Fe) SERS substrate. This high-performance, and low-cost metal–organic framework-based SERS nano sensor is capable of detecting malachite green (MG) residues in fish. The minimum detectable  concentration of MG in standard solutions is 0.1 μg/L, while in fish samples, the detection range spanned from 0.003–0.088 μg/kg. The partial least squares regression (PLSR) and support vector machine regression (SVR) were applied to model the SERS data, enhancing both the precision and reliability of the detection. The results show that compared with the traditional linear regression and PLSR models, the prediction accuracy of the SVR model is an  improvement with higher stability. MG standard solutions and three fish samples can  be analysed directly or after simple extraction. This method can be used to detect trace harmful substances in different aquatic products. Graphical

CAS / MDL: 7782-61-8
研究领域: 食品安全 · 分析化学 · 环境科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Atomically disperse Fe(III) species on the MoS2 basal plane as an efficient peracetic acid activator for water decontamination

Jingwen Wang,Yu Yang,Lei Chen,Yanping Ding,Linli Tan,Qiulin Shi,Yong Liu,Pengchao Xie

Molybdenum disulfide (MoS 2 ) is viewed as a promising two-dimensional Fenton-like catalyst, but the basal plane could not be well applied in peroxides activation. In this study, Fe(III) species were atomically impregnated on the MoS 2 basal plane to enhance peracetic acid (PAA) activation. The surface Fe(III) up shifted the d-band centre of MoS 2 and acted as electron shuttles in breaking the O-O bonds of PAA. HO • , CH 3 COO • and Fe(V) were generated in the Fe(III)-MoS 2 /PAA system, whereas the 1 O 2 production was inhibited on the Fe(III)-MoS 2 surface. Sulfamethazine (SMT) was efficiently degraded by Fe(III)-MoS 2 /PAA during 15 min reaction, with the observed removal efficiencies of SMT by Fe(III)-MoS 2 ( k obs ) being 25-fold higher than that by MoS 2 . Increasing the dosages of PAA and Fe(III)-MoS 2 facilitated SMT degradation, and high removal rate of SMT was achieved in the pH range of 3–5. HO • and Fe(V) were identified as critical reactive species responsible for the SMT degradation. Nitrification and Smiles rearrangement were proposed as the degradation pathways of SMT based on the identified oxidation products. This study demonstrates that impregnating Fe species would be an effective strategy for strengthening the Fenton-like reactivity of MoS 2 .

研究领域: 环境科学 · 化学
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APPLIED CATALYSIS A-GENERAL · 2024 · IF 4.7

Synergistic effects of adsorption and photocatalysis in MIL-88A(Fe) catalyst for remediation of phenanthrene-contaminated saline-alkaline soils

Meng Xia,Shuai Zhang,Kaihao Xu,Chengxue Zhang,Xiaocong Wang

In arid and semi-arid areas, the remediation of saline-alkaline soils polluted by organic contaminants is challenging. In this study, the adsorption–photocatalysis synergistic removal of organic contaminants was realised using the MIL-88A(Fe) catalyst, and the saline-alkaline soils were remediated simultaneously. The adsorption isotherm of catalyst conformed to Langmuir model, and the photocatalytic degradation of PHE in an optimal visible light system achieved a PHE degradation efficiency of up to 86.2 % within 30 min. Based on the identification of active oxygen species, the PHE photocatalytic degradation was primarily driven by holes (h + ) and superoxide radicals (·O 2 - ), followed by hydroxyl radicals (·OH) and singlet oxygen ( 1 O 2 ). Furthermore, the determined physical and chemical properties of the saline-alkaline soils indicated that the soil pH value decreased to 6.82, effectively increasing the absorbable nitrogen content and improving soil fertility. This study offers a new strategy for the removal of organic contaminants under special soil medium conditions.

研究领域: 环境科学 · 土壤修复
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Scientific Reports · 2016 ·Vol. 6 ·期 1 ·1-11 · IF 5.228

A novel Fe(III) dependent bioflocculant from Klebsiella oxytoca GS-4-08: culture conditions optimization and flocculation mechanism

Yu Lei,Tang Qing-wen,Zhang Yu-jia,Chen Rong-ping,Liu Xin,Qiao Wei-chuan,Li Wen-wei,Ruan Hong-hua,Song Xin

In this work, the effect of cultivation factors on the flocculation efficiency (FE) of bioflocculant P-GS408 from Klebsiella oxytoca was optimized by the response surface methodology. The most significant factor, i.e . culture time, was determined by gray relational analysis. A total of 240 mg of purified P-GS408 was prepared from 1 liter of culture solution under the optimal conditions. GC-MS analysis results indicated that the polysaccharide of P-GS408 mainly contains Rhamnose and Galactose, and the existence of abundant hydroxyl, carboxyl and amino groups was evidenced by FTIR and XPS analyses. With the aid of Fe 3+ , the FE of kaolin solution by P-GS408 could achieve 99.48% in ten minutes. Functional groups of polysaccharide were involved in the first adsorption step and the zeta potential of kaolin solution changed from −39.0 mV to 43.4 mV in the presence of Fe 3+ and P-GS408. Three-dimensional excitation-emission (EEM) fluorescence spectra demonstrates that the trivalent Fe 3+ and Al 3+ can bind efficiently with P-GS408, while those univalent and divalent cations cannot. With the help of SEM images, FTIR, zeta potential and EEM spectra, we proposed the P-GS408 flocculation mechanism, which consists of coordination bond combination, charge neutrality, adsorption and bridging, and net catching.

研究领域: 微生物学 · 环境科学
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CARBON · 2025 · IF 11.6

Modification of single atomic Fe-N4 catalytic site with sulfur to promote CO2 electroreduction

Lianzhong Shen,Lin Wang,Zhouwei Li,Yu Ye,Qizhou Dai

Atomically dispersed metal-nitrogen-carbon (M-N-C) catalysts are one of the more popular materials for electrochemical reduction of CO 2 to fuels and chemicals. Still, their Faraday efficiency and current density are generally low due to the single coordination environment and defect sites. Heteroatom doping has been demonstrated to increase the degree of defects in the material, improve the electron distribution at the single atomic sites, and enhance the catalytic performance. In this study, we prepared an S-doped single-atom catalyst called FeS@PC by a simple high-temperature pyrolysis method for efficient electroreduction of CO 2 to CO, with a maximum CO Faraday efficiency of 97.0% at -0.6 V vs. RHE potential. S atoms doped in the second-shell can change the electron distribution on the Fe-N 4 sites and accelerate the electron transfer during the electrochemical CO 2 reduction reaction (CO 2 RR). Through in situ ATR-FTIR characterization and kinetic experiments, it is found that the doped S can also promote the dissociation of H 2 O, provide sufficient protons for the conversion of CO 2 to *COOH, and promote the rate of CO conversion.

研究领域: 材料科学 · 催化化学 · 能源转换
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MICROCHEMICAL JOURNAL · 2024 · IF 4.9

A novel highly selective Fe@UiO-67-BDA/GCE sensor for efficient detecting Hg2+

Tian Si-Yu,Ding Zhu,Yao Mu-Lan,Liu Si-Mian,Hou Xiang-Yang,Tang Long,Yue Er-Lin,Wang Xiao,Wang Ji-Jiang

A three-dimensional UiO-67-BDA with various pore structures and abundant active binding sites is constructed, and Fe@UiO-67-BDA composites with electrochemical sensing and recognition performance were further prepared by successfully loading Fe 3+ ions. The different modified electrodes (Fe@UiO-67-BDA/GCE, UiO-67-BDA/GCE, Fe/GCE) and the bare electrode (GCE) were also characterized in terms of basic structure and electrochemistry, and it was found that the basic structure and electrochemical performances of Fe@UiO-67-BDA/GCE were better than those of the remaining three electrodes, with good selectivity, reproducibility and stability. And the Fe@UiO-67-BDA/GCE sensor with good electrochemical performance was constructed under the optimal working potential (E pa  = 0.59 V) and experimental conditions, which was utilized to rapidly and accurately detect heavy metal ions Hg 2+ by the DPV method, with a detection limit of up to 1.642 × 10 −9 M. In addition, the electrochemical behavior mechanism of the Fe@UiO-67- BDA/GCE sensor was investigated. Finally, the sensor was applied to detect cosmetic heavy metal ions, and the experimental results also showed high reliability and practicality. Therefore, MOFs composite material is applied to the field of electrochemistry, because of its simple operation technology, fast detection speed and high sensitivity, so that it has a greater application prospect.

CAS / MDL: 64-17-5 68-12-2
研究领域: 分析化学 · 环境科学 · 材料科学
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