CHEMICAL ENGINEERING JOURNAL
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2025
·
IF 13.2
Yiting Zhao,Yahui Wei,Shaonan Gu,Pengfei Yan,Hongbo Zhang,Jingyun Jiang,Qun Xu,Buxing Han
Utilizing renewable electricity to obtain “green” hydrogen is challenging due to the deterioration of active site activity and mass transfer capabilities at high current densities. Herein, a unique Fe-rich Ni x Fe 3−x O 4 @CP (Fe-NFC) self-supported electrode, directed by a special deep eutectic solvent (DES)-philic interface on the carbon paper (CP) collector, is developed. The Fe-NFC electrode exhibits high intrinsic catalytic activity and a stable catalyst-collector interface, enhancing oxygen evolution reaction (OER) activity and stability at elevated current densities. The regulated electronic structure of Fe-NFC is ascribed to the unique DES-philic carbon directing effect, which optimizes the adsorption energy of intermediates to further accelerate the O 2 formation during the OER process. The catalyst-collector interface also improves the mass transfer, which is favorable for the OER process at high current densities. Fe-NFC achieves a low OER overpotential of 360 mV at 1.5 A cm −2 and maintains stability for over 100 h. This work demonstrates the effectiveness of DES-interfaced engineering in optimizing active site structures and highlights the critical role of mass transport in OER at high current densities, offering a new direction for designing advanced functional materials for other gas evolution reactions.
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高影响因子
International Journal of Electrochemical Science
·
2024
·
IF 1.3
Mengling Xu,Junjie You,Chuanqing Du,Zhuotong Yu,Siqing Cheng
Prussian blue (PB) has been broadly recognized as promising cathode materials for sodium-ion batteries (SIBs) due to its large interstitial space and robust frame structure, whereas their applications are impeded by unsatisfied long-term cyclability and poor rate capability due to its inherent lattice defects. Herein, we report to fabricate the mesoporous hollow Fe 4 (Fe(CN) 6 ) 3 (one kind of PB) hierarchical nanocrystal architecture by the hydrothermal crystallization and HCl etching of the mesoporous precursor Fe 4 [Fe(CN) 6 ] 3 cubic particles, leading to high crystallinity and large specific surface area. The resultant Fe 4 [Fe(CN) 6 ] 3 cathode for SIBs exhibits a good reversibility and cycling stability with a capacity retention of 75.6 % at 0.5 C after 200 cycles as well as superb rate capability featuring a stable discharge specific capacity of 30.2 mAh g −1 at as high as 10 C, demonstrating the fast kinetics and low polarization of electrochemical reaction, which might be ascribed to the unique architecture and high crystallinity. This offers a new route to designing PB cathode of for SIBs with high rate capabilities.
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CERAMICS INTERNATIONAL
·
2024
·
IF 5.1
Shuangshuang Yang,Xingwei Wang,Chen Zhao,Chuanpeng Li,Qiangliang Yu,Bo Yu,Meirong Cai,Feng Zhou
Electromagnetic (EM) pollution frequently disrupts the regular operation of sophisticated electrical devices, necessitating the urgent development of lightweight EM wave absorbers that possess powerful absorption capability. Herein, we report a simple method for the preparation of Fe and heteroatom co-doped biochar composites (FeX-BC, where X = N, S) by directly carbonizing the precursors of anhydrous FeCl 3 , cherry kernel powder, and heteroatom dopants (melamine or Na 2 S 2 O 3 ·5H 2 O). By adding different amounts of dopants during the synthesis of the precursors, it is possible to adjust the heteroatom content of the FeX-BC samples with precision. It is worth mentioning that the FeN 0.1 -BC composite delivers the best EM wave absorption performance with an effective absorption bandwidth of 4.8 GHz and a minimal reflection loss of −63.2 dB. Furthermore, the significant attenuation of EM wave can be attributed to the synergistic interplay of magnetic loss, dielectric loss and the enhanced impedance matching. This study introduces a simple methodology for the fabrication of EM wave absorbers, a significant contribution to the synthesis, advancement, and functional applications of biomass-derived materials.
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ChemistrySelect
·
2024
·Vol. 9
·期 8
·e202303088
·
IF 1.9
Xiayan Zhang,Zhi Song,Boxia Liu,Jialu Liu,Yeqiong Huang,Dongxu Han
Graphical Ni/Fe bimetallic atom cluster catalyst is prepared by a hydrothermal to stimulate PMS to produce high concentration 1 O 2 and efficiently remove BPA from aqueous solution. It is found that 1 O 2 in the system is the most important active component in the degradation process of BPA, and a high concentration of 1 O 2 could promote the rapid degradation of BPA in solution. The advanced oxidation process based on peroxymonosulfate (PMS) is a new water purification strategy. In this work, Ni/Fe bimetallic atom cluster composite catalyst is prepared by a hydrothermal synthesis to stimulate PMS to produce high concentration singlet oxygen ( 1 O 2 ) and efficiently remove bisphenol A (BPA) from aqueous solution. The experimental data show that in a broad pH range (pH=3–11), the removal rate of BPA by the non-free radical pathway induced by 1 O 2 is close to 100 %, and the catalyst still has high stability after 5 cycles. The mechanism of BPA removal in NiFe−BC/PMS/BPA catalytic degradation system is investigated by quenching experiment. It is found that 1 O 2 in the system is the most important active component in the degradation process of BPA, and a high concentration of 1 O 2 could promote the rapid degradation of BPA in solution. In this paper, the high catalytic activity and selectivity of bimetallic atomic cluster catalysts can provide new insights for the treatment of phenolic wastewater.
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COLLOIDS AND SURFACES B-BIOINTERFACES
·
2024
·
IF 5.4
Na Li,Jing Tang,Congxiao Wang,Minghui Wang,Guodong Chen,Lei Jiao,Qinglai Yang,Xiaofeng Tan
The rational design of nanozymes with highly efficient reactive oxygen species (ROS) generation to overcome the resistant infection microenvironment still faces a significant challenge. Herein, the highly active Fe single-atom nanozymes (Fe SAzymes) with a hierarchically porous nanostructure were prepared through a colloidal silica-induced template method. The proposed Fe SAzymes with satisfactory oxidase (OD)-like and peroxidase (POD)-like activity can transform O 2 and H 2 O 2 to superoxide anion free radical (•O 2 - ) and hydroxyl radical (•OH), which possess an excellent bactericidal effect. Also, the glutathione peroxidase (GPX)-like activity of Fe SAzymes can consume glutathione in the infection microenvironment, thus facilitating ROS generation to enhance the sterilization effect. Besides, the intrinsic photothermal effect of Fe SAzymes further significantly boosts the enzyme-like activity to generate much more reactive oxygen species for efficient antibacterial therapy. Accordingly, both in vitro and in vivo results indicate that the Fe SAzymes with synergistically photothermal-catalytic performances exhibit satisfactory antibacterial effects and biocompatibility. This work provides new insights into designing highly efficient SAzymes for effective sterilization applications by an amount of ROS generation.
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PubMed
高影响因子
MICROCHEMICAL JOURNAL
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2025
·
IF 5.1
Xue Zhang,Shihan Kang,Wangxing Cheng,Lei Wang,Nannan Lu,Lin-Wei Chen
Establishing an efficient and sensitive electrochemical sensor for paracetamol (PCM) is of significant importance in pharmaceutical quality control and environmental protection. This paper reports a novel electrochemical sensing platform based on a ZIF-8-derived strategy for fabricating N-doped porous carbon with monodispersed Fe-N x sites (Fe-N/NPC). The introduction of iron phthalocyanine (Fe-Pc) molecules fixed within the ZIF-8 framework prevents the aggregation of metal species during high-temperature treatment, ensuring the high dispersion of Fe-N x sites. Under optimized conditions, Fe-N/NPC-10/GCE electrochemical sensor exhibits excellent performance for PCM detection, which is mainly attributed to the synergistic enhancement between Fe-N x and NPC. The high surface area of NPC with a porous structure and N doping effect, which enhances its adsorption capacity for PCM, facilitating electron transfer and thereby amplifying the response signal. At the same time, the high-density monodispersed Fe-N x provides abundant catalytic active sites, improving electrocatalytic activity. Through the investigation of how buffer solution pH affects the oxidation peak induced by PCM, a pH of 7.0 was ultimately determined to be the optimal value. Using differential pulse voltammetry (DPV), the Fe-N/NPC-10/GCE electrochemical sensor demonstrates a wide detection range (0.1–10, 10–150 μM) for PCM with a detection limit (LOD) of 0.019 μM. Furthermore, the sensor exhibits good selectivity, stability, and reproducibility, and has been successfully applied for the determination of PCM in real pharmaceutical samples, with a recovery rate close to 100 %, indicating that the analytical method performs well and is suitable for analysis of real samples.
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Journal of Environmental Sciences
·
2018
·
IF 3.12
Tuqiao Zhang,Feilong Dong,Feng Luo,Cong Li
Sulfonamides are used in human therapy, animal husbandry and agriculture but are not easily biodegradable, and are often detected in surface water. Sulfamethazine (SMZ) and sulfadiazine (SDZ) are two widely used sulfonamide antibiotics that are used heavily in agriculture. In this study, they were degraded in an aqueous system by chlorination after pre-oxidation with ferrate(VI) (Fe VI O 4 2 − , Fe(VI)), an environmentally friendly oxidation technique that has been shown to be effective in degrading various organics. The kinetics of the degradation were determined as a function of Fe(VI) (0–1.5 mg/L), free chlorine (0–1.8 mg/L) and temperature (15–35°C). According to the experimental results, SMZ chlorination followed second-order kinetics with increasing Fe(VI) dosage, and the effect of the initial free chlorine concentration on the reaction kinetics with pre-oxidation by Fe(VI) fitted a pseudo-first order model. The rate constants of SDZ and SMZ chlorination at different temperatures were related to the Arrhenius equation. Fe(VI) could reduce the levels of THMs formed and the toxicity of the sulfonamide degradation systems with Fe(VI) doses of 0.5–1.5 mg/L, which provides a reference for ensuring water quality in drinking water systems.
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高影响因子
Journal of Analysis and Testing
·
2018
·Vol. 2
·期 1
·69-76
·
IF 0
Zhen Wen-Yao,Bai Jing,Jia Xiao-Dan,Wu Lie,Jiang Xiu-E
The local tumor hypoxia has become one of the main obstacles for photodynamic therapy (PDT).To break through this barrier, the fabrication of O 2 -evolving nanoplatform has been more significant. Herein, the uniform methylene blue (MB)–bovine serum albumin (BSA)–Fe(III) nanoparticles (MB–BSA–Fe(III) NPs) were successfully synthesized by biomineralization approach. MB–BSA–Fe(III) NPs show high loading capacity of MB, and Fe(ΙΙΙ) has excellent catalytic performance towards abundant H 2 O 2 in cancer cells to generate O 2 , overcoming tumor hypoxia. All these combination effects remarkably increase the therapeutic efficiency of PDT, resulting in almost complete destruction of cancer cells. Most importantly, MB–BSA–Fe(III) NPs exhibit T 2- magnetic resonance imaging, which have the potential for precise visualization of the tumor location. Our results demonstrate that MB–BSA–Fe(III) is a novel H 2 O 2 -responsive and O 2 -evolving nanoplatform and it has great potential for clinical applications such as cancer diagnosis, treatment or drug delivery.
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JOURNAL OF HAZARDOUS MATERIALS
·
2017
·
IF 6.065
Weirui Chen,Xukai Li,Yiming Tang,Jialu Zhou,Dan Wu,Yin Wu,Laisheng Li
A flexible catalyst, Fe-Cu-MCM-41, was employed to enhance diclofenac (DCF) mineralization and inhibit bromate formation in catalytic ozonation process. Greater TOC removal was achieved in Fe-Cu-MCM-41/O 3 process (78%) than those in Fe-MCM-41/O 3 (65%), Cu-MCM-41/O 3 (73%) and sole ozonation (42%). But it was interesting that both Cu-MCM-41/O 3 and Fe-MCM-41/O 3 achieved 93% bromate inhibition efficiency, only 71% inhibition efficiency was observed in Fe-Cu-MCM-41/O 3 . Influence of pH, TBA/NaHSO 3 and detection of by-products were conducted to explore the mechanism. By Pyridine adsorption–IR and XPS, a relationship was found among activity of catalysts, Lewis acid sites and electron transfer effect between Fe (II/III) and Cu (I/II). Fe-Cu-MCM-41 promoted ozone decomposition to generate OH, which accounted for enhanced DCF mineralization. The consumption of aqueous O 3 also suppressed the oxidative of Br − and HBrO/Br − . More HBrO/BrO − accumulated in catalytic ozonation process and less bromate generated. Bromate formation in Fe-Cu-MCM-41/O 3 process was sensitive with pH value, the acidic condition was not favor for bromate formation. Both DCF mineralization and bromate inhibition were influenced by surface reaction. Moreover, Fe-Cu-MCM-41 showed excellent catalytic performance in suppressing the accumulation of carboxylic acid, especially for oxalic acid. Nearly no oxalic acid was detected during Fe-Cu-MCM-41/O 3 process.
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高影响因子
Journal of Materials Chemistry C
·
2017
·Vol. 6
·期 3
·558-567
·
IF 5.256
Xueai Li,Daxue Du,Chunsheng Wang,Haiyan Wang,Zhaopeng Xu
To satisfy the requirements of high-performance electromagnetic wave absorbers, composites of carbon and ferromagnetic metal with designed morphologies and abundant interfaces are highly desirable to balance impedance matching and attenuation. However, the synthesis of composites to meet these requirements and analysis of the electromagnetic wave energy loss mechanism remain great challenges. In this study, hierarchical rose-like assemblies of carbon–wrapped iron (Fe@C) nanoparticles with a porous structure were successfully synthesized via an in situ route using an iron alkoxide precursor with a rose-like morphology. Under the studied pyrolysis atmosphere and temperature, rose-like Fe@C and pure iron can be well modulated. The carbon shell is graphitic and highly ordered due to the catalytic effects of the iron nanoparticles, which affect the electromagnetic properties of the composites. The electromagnetic wave absorption properties of the Fe@C composite and iron are estimated in the frequency range of 2.0–18.0 GHz, and as expected, the hierarchical rose-like porous Fe@C demonstrates outstanding reflection loss characteristics with a minimum value of −71.47 dB with a thin matched thickness of 1.48 mm. Moreover, an ultra-wide response bandwidth (reflection loss of less than −10 dB) of 2.88–18.0 GHz is achieved. Analysis of the electromagnetic properties revealed that the hierarchical rose-like Fe@C presents very different electromagnetic functions in comparison to pure iron and Fe@C particles without the rose-like structure derived from the iron alkoxide precursor with the same structure. The carbon shells and special morphology with a certain microstructure can effectively regulate the complex permittivity and permeability to modify the impedance matching characteristic as well as enhance the attenuation ability via electromagnetic wave multiple reflection and scattering in the hierarchical rose-like Fe@C particles. Analysis of the attenuation constant and matched characteristic impedance validates that the enhanced electromagnetic wave absorption of the rose-like Fe@C with a porous structure is due to the significant enhancement of matched impedance and collective multiple loss mechanism.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Wentao Li,Qian Zhang,Zuohua Liu,Changyuan Tao,Guocan Zheng,Nanxiong Chen,Dong Wang,Hufei Chen
The long-term accumulation of manganese sulfate residues can lead to the release of soluble manganese ions, thereby contaminating the surrounding environment. Although numerous methods exist to address the issue of soluble manganese ions, current harmless treatment approaches fail to consider the subsequent utilization of manganese slag. This study aims to control the magnetic properties of processed residues by adjusting the addition of barium hydroxide and the reaction duration. Our results reveal that the harmless treatment of manganese sulfate slag is achievable with various amounts of barium hydroxide, and the magnetic properties of the reconstructed slag increase with the increased barium hydroxide dosage. Magnetic separation is employed to separate the magnetic components from the reconstructed slag, and the distribution state of these magnetic substance is modulated by altering the particle size and reagent addition. Under optimal conditions, this study finds that the grade of iron was 24.17 %, the grade of manganese was 8.08 %, and the recovery could reach 79 % for iron and 70 % for manganese. Finally, the fining slag obtained by magnetic separation was utilized as an additive in the preparation of ferrites, reducing the minimum reflection loss of the ferrites to −16.18 dB, signifying up to 90 % electromagnetic wave attenuation. These findings indicate that the fining slags holds great potential as a dopant for ferrites, offering a viable pathway for the resourceful and environmentally friendly treatment of manganese sulfate residues.
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APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Di Wang,Jing Wang,Yiqiang Wu,Delin Sun,Wenlei Wang
Transition metal ions and non-metal co-doped carbon-based materials have attracted extensive attention due to their unique properties and excellent catalytic effect. Fe 2 O 3 /TiO 2 @Fe/Ti-N-C multifunctional photocatalyst with Fe-Ti alloy and abundant nitrogen defects was reported. The photocatalytic results showed that the removal rates of Cr (VI), Congo red (CR) and levofloxacin (LFX) in water by Fe 2 O 3 /TiO 2 @Fe/Ti-N-C were 88.46, 96.71 and 99.06 %, respectively. The photoelectric test results show that bimetallic conjugated structure of Fe and Ti can effectively increase the light absorption range and accelerate the carrier separation. N-defects can significantly increase the lifetime and concentration of photogenerated holes, thereby improving the catalytic efficiency of the photocatalyst. The single factor experiments proved that the optimal pH for the degradation of Cr(VI), CR and LFX by Fe 2 O 3 /TiO 2 @Fe/Ti-N-C was 1, 11 and 9, respectively. In addition, Ca 2+ and Mg 2+ promoted the degradation of Cr(VI) and inhibited the degradation of CR and LFX. SO 4 2- inhibited the degradation of Cr(VI) and promoted the degradation of CR and LFX. Cl - inhibited the degradation of Cr(VI), CR and LFX. This study elucidates the mechanism of N-defects and bimetallic sites in photocatalytic reactions, and provides theoretical support for efficient removal of heavy metals and organic pollutants in water.
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