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CERAMICS INTERNATIONAL · 2017 ·Vol. 43 ·期 17 ·15551-15555 · IF 2.986

Wave absorbing performance of polymer-derived SiCN(Fe) ceramics

Youzhi Wang,Xue Guo,Yurun Feng,Xiao Lin,Hongyu Gong

Ferreous polymer-derived SiCN ceramics (PDCs-SiCN(Fe)) were successfully synthesized by precursor conversion method. The phase composition and microstructure of the obtained products were investigated by XRD , SEM and TEM . The result indicated a mainly amorphous structure with a few α-Fe,and graphite phases in the gaps. The conductivity, electromagnetic parameters and wave absorbing properties of the prepared ceramics were studied at the frequency band from 2 to 18   GHz. The reflectance of PDCs-SiCN(Fe) was about −10   dB (> 90% absorption) in the range of 4–16   GHz with 25   wt% nano-Fe 2 O 3 addition at the thickness 8   mm. The maximum value of dielectric and magnetic loss angle tangent was about 1.5, indicating PDCs-SiCN(Fe) ceramics possessed good absorption performance .

研究领域: 材料科学 · 陶瓷学 · 电磁学 · 功能材料 · 复合材料
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Synergizing RuO2 with Fe-doped Co2RuO4 for boosting alkaline electrocatalytic oxygen evolution reaction

Mengyue Qi,Huamei Tong,Gaojie Li,Xinyu Zheng,Yu Liu,Cheng Ye,Zaoxue Yan,Deli Jiang

Designing and development of electrocatalysts with high catalytic capacity and stability for oxygen evolution reaction (OER) is significant for sustainable water splitting. In this study, we rationally designed Fe-doped Co 2 RuO 4 /RuO 2 heterostructure electrocatalysts on nickel foam (NF) through mixture hydrothermal, ion exchanging, and calcining methods. The synergistic effect between the Fe-Co 2 RuO 4 /RuO 2 heterogeneous interfaces can result in superior inherent activity. Meanwhile, the unique nanosheet on nanosheet structure delivers abundant exposed active sites, leading to improved catalytic activity. The resultant Fe-Co 2 RuO 4 /RuO 2 heterostructured catalysts possessed superior OER property, attaining a current density of 50 mA cm −2 with only 253 mV overpotential in 1.0 M KOH alkaline solution, and demonstrating good durability with continuous operation for up to 50 h. This research provides robust support for the research and development of RuO 2 -based electrocatalysts through effective interface engineering and doping strategies, and opens up new avenues for the industrial application of water splitting technology.

研究领域: 材料科学 · 能源化学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2021 · IF 8.128

Engineering of bionic Fe/Mo bimetallene for boosting the photocatalytic nitrogen reduction performance

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.

研究领域: 材料科学 · 催化化学 · 环境科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Fe-nanocluster embedded biomass-derived carbon for efficient photo-Fenton-like activity in water purification

Xin Li,Wanrong Bu,Ke Zhu,Yuwen Chen,Xiaoying Liang,Bin Wang,Yuchen Wang,Kai Yan

Single-atom catalysts (SACs) as photo-Fenton-like catalysts have attracted widespread attention in water purification. However, the development of SACs with renewability, cleanliness, high mass loading, and raw material abundance is a formidable challenge to achieve efficient pollutant removal. In this study, we fabricated high-performance Fe-nanocluster embedded biomass-derived carbon (Fe/Bio-C) from Ficus altissima wastes for quinolone antibiotics degradation. The high-angle annular dark-field scanning transmission electron microscopy with aberration correction (AC-HAADF-STEM) and X-ray absorption fine structure spectroscopy (XAFS) revealed that the Fe/Bio-C exhibited a porous structure with abundant Fe-N 4 active sites. The Fe/Bio-C catalysts achieved an exceptional efficiency of 98.6 % for the removal of the representative quinolone antibiotic, namely lomefloxacin (LOM), within 30 min. Furthermore, an in-depth exploration was conducted to assess the influence of reaction parameters on degradation performance, kinetics, toxicity, and mechanism. The free radical quenching experiments and electron paramagnetic resonance (EPR) spectra demonstrated the existence of ·O 2 − , 1 O 2 , ·OH, SO 4 · − in the reaction system and the ·O 2 − radicals played a relatively important role in the degradation progress. This work broaden the avenue for constructing metal-nanocluster photocatalysts with the high reactivity, low metal leaching, and universality to various pollutants.

CAS / MDL: 10025-77-1 298-14-6
研究领域: 环境科学 · 材料科学 · 化学工程 · 水处理
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APPLIED ORGANOMETALLIC CHEMISTRY · 2024 · IF 3.7

Cobalt-Potassium Synergistic Modification Effects on Fe-Based Catalysts for CO2 Hydrogenation to Low-Carbon Olefins

Yi Jing Jia,Jin Quan Tao,Hao Ran Liu,Wen Bin Huang,Rongpeng Yao,Miaomiao Niu,Rongrong Li,Qiang Wei,Ya Song Zhou

To enhance the CO 2 hydrogenation activity and low-carbon olefin selectivity of Fe-based catalysts, a strategy involving the use of metal promoters to modulate the structure of active metal centers in catalyst preparation was proposed. The incipient wetness impregnation method was used to introduce modifying agents K and/or Co into the Fe/Al 2 O 3 catalyst. Characterization techniques such as XRD, BET, SEM, HRTEM, H 2 -TPR, XPS, CO 2 -TPD, NH 3 -TPD, and TG were employed to investigate the effects of the modifying agents on the dispersion, reducibility, electronic properties, and acid–base properties of active metal species. Furthermore, the influence of K and Co modification on the CO 2 hydrogenation activity and low-carbon olefin selectivity of Fe/Al 2 O 3 catalysts was explored. The results revealed that the introduction of K generated more basic sites and electron-rich active metal centers in the catalyst, facilitating the adsorption and activation of CO 2 , while suppressing the hydrogenation of olefins and the formation of methane, thus improving the selectivity towards low-carbon olefins. Co promoter facilitated the dispersion of Fe species, exposing more active sites and enhancing the FTS reaction activity, leading to more CO being converted into C 2+ hydrocarbon products. Under the synergistic effect of K and Co, the CO 2 conversion activity of the Fe-based catalyst significantly increased, achieving a CO 2 conversion rate of 37%, while the selectivity towards C 2 -C 4= increased to 31.9%.

研究领域: 催化化学 · 材料科学
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MICROCHEMICAL JOURNAL · 2025 · IF 5.1

Fe/Fe3C anchored on activated N-doped porous carbon for sensitive and selective determination of levodopa

Yong Xu,Shi Chen,Mingfu Ye,Mingyue Wang,Wenhai Wang,Konglin Wu

Levodopa (LDA) is a principal medication for the treatment of Parkinson’s disease, with its therapeutic efficacy and potential side effects being closely associated with administered dosages. Consequently, the development of sophisticated LDA detection methods is of significant importance. Herein, we present the successful fabrication of an innovative electrochemical sensor utilizing Fe/Fe 3 C nanoparticles supported on activated N-doped carbon spheres (Fe/Fe 3 C-ANC), which makes full use of the large specific area of ANC to accommodate more dispersive Fe/Fe 3 C NPs that exhibits outstanding electrocatalytic activity for LDA oxidation. The experimental findings demonstrate that Fe/Fe 3 C-ANC sensor can deliver wide linear response ranges (1–40 µM) with an impressively low limit of detection of 0.22 µM, surpassing the performance of most previously reported electrochemical sensors. Additionally, the good selectivity of Fe/Fe 3 C-ANC sensor was also proved through measuring a series of LDA structural analogues and potential interfering substances. Furthermore, its excellent selectivity was confirmed through the analysis of LDA structural analogs and potential interferents. The practical utility of the sensor was evaluated by detecting LDA in commercial tablets, spiked human serum and spiked artificial cerebrospinal fluid samples.

研究领域: 医学 · 材料科学 · 分析化学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2021 · IF 8.128

Indium sulfide deposited MIL-53(Fe) microrods: Efficient visible-light-driven photocatalytic reduction of hexavalent chromium

Linbo Luo,Sheying Dong,Hao Cui,Longhui Sun,Tinglin Huang

The ecosystems and human health were seriously threatened by hexavalent chromium (Cr(VI)) in wastewater. In this article, using the idea of the highly matched energy band structure between indium sulfide (In 2 S 3 ) and MIL-53(Fe), a Type-II heterojunction has been constructed by loading In 2 S 3 on MIL-53(Fe) microrod to overcome the fault like high recombination rates of photogenerated electron-holes of In 2 S 3 . The composite with 20:1 mass ratio of In 2 S 3 to MIL-53(Fe) (IM-2) was adopted as an optimal sample for efficient photocatalytic Cr(VI) reduction under visible light . Various characterization techniques were used to verify the characteristics of composites and delved into the structure-effect relationship between this heterojunction and its activity. Results showed that the reaction rate constants of the photoreduction process over IM-2 was ~ 4 and 26 times higher than those of pure In 2 S 3 and MIL-53(Fe), respectively, and the catalyst could maintain superior removal efficiency (88.6%) and steady crystal structure after four cycles. First-principles calculations further illustrated that the heterostructure formed between In 2 S 3 and MIL-53(Fe) could effectively accelerate the separation of photogenerated electrons and holes, thus improving the photocatalytic reduction performance. Moreover, the active species analyses revealed that the superoxide radicals and electrons were mainly involved in the reduction of Cr(VI).

研究领域: 环境科学 · 材料科学
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2021 · IF 4.464

Enzyme-like Fe-N5 single atom catalyst for simultaneous electrochemical detection of dopamine and uric acid

Fuad Abduro Bushira,Shimeles Addisu Kitte,Haijuan Li,Lirong Zheng,Ping Wang,Yongdong Jin

Simultaneous highly sensitive and accurate detection of dopamine (DA) and uric acid (UA) is of great importance since they are important biomolecules that are commonly coexisted in the human body and play a crucial role in numerous physiological and pathological features. In this work, Fe-N 5 single atom catalyst (SAC) supported on graphene was firstly employed for simultaneous electrochemical detection DA and UA. Owing to its unique electronic structure and abundant active sites, under optimal conditions, the enzyme-like Fe-N 5 SAC constructed electrochemical (bio)sensor exhibits excellent linear characteristic responses in the range of 0.005–500 and 0.01–480 µM, as well as the low limit of detection of 0.007 and 0.027 nM for DA and UA, respectively. More critically, the developed electrochemical system shows promising merits of exceptional stability, good repeatability, and, consequently, it was successfully applied for simultaneous sensitive detection of DA and UA in human serum samples.

研究领域: 生物医学工程 · 分析化学
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Journal of Functional Biomaterials · 2024 ·Vol. 15 ·期 7 ·185 · IF 5

A Type of Ferrocene-Based Derivative FE-1 COF Material for Glycopeptide and Phosphopeptide Selective Enrichment

Yu Wu,Sen Xu,Fengjuan Ding,Weibing Zhang,Haiyan Liu

In this work, a new type of FE-1 COF material is prepared by a reversible imine condensation reaction with diaminoferrocene and diaminodiformaldehyde as materials. The material is connected by imine bonds to form a COF skeleton, and the presence of plenty of nitrogen-containing groups gives the material good hydrophilicity; the presence of metal Fe ions provides the material application potential in the enrichment of phosphopeptides. According to the different binding abilities of N-glycopeptide and phosphopeptide on FE-1 COF, it can simultaneously enrich N-glycopeptide and phosphopeptide through different elution conditions to realize its controllable and selective enrichment. Using the above characteristics, 18 phosphopeptides were detected from α-casein hydrolysate, 8 phosphopeptides were detected from β-casein hydrolysate and 21 glycopeptides were detected from IgG hydrolysate. Finally, the gradual elution strategy was used; 16 phosphopeptides and 19 glycopeptides were detected from the α-casein hydrolysate and IgG hydrolysate. The corresponding glycopeptides and phosphopeptides were identified from the human serum. It proves that the FE-1 COF material has a good enrichment effect on phosphopeptides and glycopeptides.

研究领域: 分析化学 · 蛋白质组学 · 生物化学
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Biomaterials Science · 2018 ·Vol. 6 ·期 5 ·1227-1237 · IF 5.831

Regulating the local pH level of titanium via Mg–Fe layered double hydroxides films for enhanced osteogenesis

Qianwen Li,Donghui Wang,Jiajun Qiu,Feng Peng,Xuanyong Liu

Hard tissue implant materials which can cause a suitable alkaline microenvironment are thought to be beneficial for stimulating osteoblast differentiation while suppressing osteoclast generation. To make the local pH around the interface between materials and cells controllable, we prepared a series of Mg–Fe layered double hydroxide (LDH) films on acid-etched pure titanium surfaces via hydrothermal treatment. By adjusting the Mg/Fe proportion ratio, the interlayer spacing of Mg–Fe LDHs was regulated, making their OH− exchange abilities adjustable, and this ultimately resulted in a microenvironment with a controllable pH value. In vitro experiments demonstrated that the Mg–Fe LDH film-modified titanium surface possessed good biocompatibility and osteogenic activity, especially the Mg–Fe LDH film with Mg/Fe proportion ratio of 4, which could form a suitable alkaline microenvironment for the growth and osteogenetic differentiation of stem cells. These results demonstrate the potential application of the prepared Mg–Fe LDH films in enhancing the osteogenesis of implant materials while providing a new way into the design of controllable alkaline environment.

研究领域: 生物材料学 · 细胞生物学 · 医学工程
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Journal of Materials Chemistry C · 2024 · IF 5.7

Soft Actuators based on MIL-88B(Fe) flexible MOF with Fast Response to Various Organic Solvent Vapor

Shizhen Song,Tengfei Zheng,Bo Li,Hangcheng Yang,Qin-Xiang Jia,Zhuting Hao,Wen Zhang,Ying Zhang

Solvent vapor-driven soft actuators have been seen as promising devices for human-environment interaction and gained considerable attention in recent years. Considering the limited types of response solvent and the lack of quantification, MOF/polymer intelligent soft actuators may be a potential candidate of the fabrication of the bio solvent-driven actuators. Thus, this paper present a multiple solvent-driven soft actuator based on MIL-88B/PVDF asymmetric film, and also the comparison to the analogs based on other MIL-88(Fe) series flexible MOFs (including MIL-88A, 88C and 88D) was made for the deformation-structure relationship and the solvent-driven mechanism investigation. The deformation behavior to various organic solvent (including methanol, toluene and chloroform) of the MIL-88(Fe)/PVDF composite films have been investigated, and the structure and composition of the MIL88(Fe) fillers and the composite films were also characterized by SEM, FT-IR, and XRD. Based on the above results, the MIL-88B/PVDF composite which shows the diversity of response objects and the fast deformation response to most of the organic solvents through the solvent swelling/adsorption of the MOF skeleton, was used to fabricate a monolayer soft film composed by MIL-88B, carbon black (CB) and PVDF, namely MIL-88B/CB/PVDF. The MIL-88B/CB/PVDF film not only realizes the excellent deformation-discolor dual-responsive to methanol atmosphere with the visible deformation which could being quickly achieved within 1s under 10 vol % methanol atmosphere and the maximum crimp angle being up to 558o within about 50 s, and also a wide color change range including six view angle-dependent high saturation color (red, orange, yellow, green, blue and purple), but also shows an approximate linear relationship to three of the organic solvents (methanol, toluene and chloroform) between the maximum curl angle and the solvent concentration. Furthermore, several smart devices have also been fabricated, including the methanol-driven bionic petals, worm robot, alertor and LIG sensor. Therefore, such soft composites of flexible MOF and polymer have great potential in bio-robot and this work may provide new design strategy for the MOFs/polymer smart materials.

研究领域: 材料科学 · 化学工程
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Desalination and Water Treatment · 2024 · IF 1

Adsorption of neutral red onto MIL-100(Fe) from solution: characterization, equilibrium, kinetics, thermodynamics and process design

Shanshan Chen,Kang Wen,Xiaoting Zhang,Ruize Zhang,Runping Han

Metal organic frameworks are attracting scientific interest in adsorption applications owing to their large surface area and controllable pore size or shape over both microporous and mesoporous domains. Based on this, an iron(III) trimesic acid MIL-100(Fe) was facilely synthesized by hydrothermal treatment and used as adsorbent to remove neutral red (NR) from aqueous solution. MIL-100(Fe) was characterized using X-ray diffraction, scanning electron microscopy and transform infrared spectroscopy. MIL-100(Fe) was studied in view of the adsorption isotherms, thermodynamics, kinetics, and regeneration of the adsorbent. The adsorption kinetics data of NR were found to be in agreement with pseudo-second-order model. Temkin model was observed to be more suitable than Freundlich and Langmuir models in describing the adsorption isotherm. The maximum adsorption quantity was 333 mg g –1 at 313 K from Langmuir model. Thermodynamic parameters indicated that the NR adsorption process was endothermic and spontaneous. The NR-loaded MIL-100(Fe) adsorbent was regenerated and reused using pH = 2, 75% ethanol. A single-stage batch design for NR adsorption onto MIL-100(Fe) was also presented based on Temkin isotherm model equation. Based on the findings, MIL-100(Fe) is a promising adsorbent for the removal of cationic dyes from solution and thus can be used in practical application.

研究领域: 环境科学 · 材料科学 · 化学工程
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