CHEMICAL ENGINEERING JOURNAL
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2024
·
IF 13.3
Huimin Li,Zhe Sun,Chenlong Dong,Xueli Zhang,Chengkun Lei,Baobao Jin,Qianqian Shen,Husheng Jia,Jinbo Xue
Photocatalytic non-oxidative coupling of methane is an attractive strategy for CH 4 to C 2 conversion, how to facilitate the photogenerated charge separation and accelerate the C–C coupling to promote the reaction kinetics remains a great challenge. Herein, a symbiotic r-Fe 2 O 3 /NiO heterostructure with robust interfaces is constructed in situ. The coherent interface not only provides unique Ni–O–Fe asymmetric sites, but also achieves the separation and transport of photogenerated charge. The unbalanced charge density distribution of two adjacent methyl or methylene at the Ni–O–Fe asymmetric site alleviates the dipole repulsion of the C–C coupling, and promotes C–C coupling to form C 2 hydrocarbons. Under visible light irradiation, the optimal r-Fe 2 O 3 /NiO performs a brilliant C 2 activity up to 71.00 μmol g −1 h −1 , and the C 2 H 4 yield can reach a high value of 40.46 μmol g −1 h −1 and the selectivity of 56.98 %. This work provides new insights into the coupling of C–C to generate C 2 hydrocarbons.
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ENVIRONMENTAL POLLUTION
·
2024
·
IF 7.6
Miaofei Sun,Sajjad Ali,Chengyin Liu,Chunhui Dai,Xin Liu,Chao Zeng
In this work, a series of hydrogenated Fe-doped AgIO 3 (FAI-x) catalysts are synthesized for photodegrading diverse azo dyes and antibiotics. Under the irradiation of natural sunlight with a light intensity of ∼60 mW/cm 2 , the optimum FAI-10 exhibits a considerable rate constant for decomposing methyl orange (MO) of 0.067 min −1 , about 7.4 times higher than that of AgIO 3 (0.009 min −1 ), and 24.6% and 83.8% of MO can be decomposed over AgIO 3 and FAI-10 after irradiation for 40 min. In the amplification photodegradation experiments with using 0.5 g catalyst and 400 mL MO dye solution (10 mg/L), FAI-10 possesses greatly higher photoreactivity to common semiconductors (ZnO, TiO 2 , In 2 O 3 and Bi 2 MoO 6 ), and the photodegradation rates over FAI-10 are 92%. Particularly, the FAI-10 shows superior stability, the activity of which remains unaltered after 8 continuous cycles. Foreign ions and water bodies have slight effect on the activity of FAI-10, but the MO degradation rates are decreased by adjusting pH values, especially when pH = 11 because of the strong electrostatic repulsion between MO and FAI-10. FAI-10 can also effectively decompose another azo dye (rhodamine B (RhB)) and diverse antibiotics (sulflsoxazole (SOX), chlortetracycline hydrochloride (CTC), tetracycline hydrochloride (TC) and ofloxacin (OFX)). The activity enhancement mechanism of FAI-10 has been systemically investigated and is ascribed to the promoted photo-absorption, charge separation and transfer efficiency, and affinity of organic pollutants , owing to the synergistic effect of Fe doping and oxygen vacancy (Ov). The photocatalytic mechanisms and process for decomposing MO are verified and proposed based on radical trapping experiments and liquid chromatography-mass spectrometry (LC-MS). This work opens an avenue for the fabrication of effective photocatalysts toward water purification .
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ELECTROCHIMICA ACTA
·
2024
·
IF 5.5
Ke Qu,Yuhang Qiu,Miao Deng
Conforming to the principles of green chemistry and sustainable environmental progress, this work demonstrated the concept of “treating waste with waste”, i.e. treating atmospheric pollutant sulfur dioxide (SO 2 ) with agricultural waste of tangerine peel. SO 2 electro-catalytic oxidation is the key technique in this endeavor, which utilizes SO 2 as reaction raw material in the anode to remove it. The anodic SO 2 electro-catalytic oxidation could be coupled to the cathodic hydrogen evolution to achieve the simultaneous SO 2 removal and hydrogen production. Anodic catalyst plays a vital role in this SO 2 transformation. In this work, tangerine peel has been re-utilized to afford tangerine peel-derived biochar (TPB) to prepare TPB/CNT-derived Fe 3 C/Fe/C (N-doped) as a capable anodic catalyst to achieve this goal. With help of various characterization techniques and electrochemical testing, the optimal iron mass fraction and pyrolysis temperature were found to be 16 wt% Fe under 800 °C, with carboxylated carbon nanotube as carbon additive. Transmission electron microscopy (TEM) image showed that the as-prepared TPB/CNT-derived Fe 3 C/Fe/C (N-doped) featured a unique morphology to encapsulate Fe 3 C/Fe with a layer of protecting carbon, which should contribute to the enhanced electro-catalytic performances. A flow electrolyzer was also assembled to illustrate practical application of the anodic catalyst in the real scenario. Owing to its lower cost, the as-prepared TPB/CNT-derived Fe 3 C/Fe/C (N-doped) will be advantageous to replace precious metals to mediate SO 2 electro-catalytic oxidation as one of promising environmental treatment techniques in the future.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2024
·Vol. 31
·期 47
·57822-57831
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IF 0
Liu Yifan,Xu Zhuangqin,He Yuting,Liu Minghua,Lin Chunxiang,Lv Yuancai
A synergistic photocatalytic system based on Fe-based perovskite with persulfate was constructed for alkali lignin (AL) degradation in pulp and paper wastewater. The degradation performance and mechanism on AL were carried out under ambient temperature and pressure, accompanied by visible light irradiation. The results showed that the synergistic photocatalytic system exhibited much better performance on AL degradation than the single catalytic system. The degradation efficiency reached 73.5% under the optimal conditions and was constant at around 65% over the pH range from 2 to 8. A significant escalation of the AL degradation was observed at pH 10, reaching 80.1%. The photogenerated holes, 1 O 2 and SO 4 − ·, generated by the system were involved in the degradation, and the holes played a dominant role. During the degradation process, the efficient promotion of cleavage events in lignin methoxy, β -O-4 bond, and benzene ring was observed. Consequently, the depolymerization process led to the generation of high-value compounds, namely p -hydroxybenzaldehyde and vanillin. Remarkably, the yields of the high-value compounds in the synergistic photocatalytic system were five times larger than those in the control. This study offered a viable method to activate persulfate for alkali lignin degradation and to achieve a mutually beneficial strategy for wastewater treatment and recycling.
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ChemPlusChem
·
2024
·
IF 3
Meng-Ge Wei,Hong-Ru Li,Liang-Nian He
Graphical A series of solid base KF/Mg-Fe bi-metal oxides were fabricated via supporting KF on Mg-Fe bi-metal oxides and calcination. When applied as catalyst to dimethyl carbonate (DMC) synthesis through transesterification of ethylene carbonate (EC) and methanol, this material can afford up to 88 % yield and 97 % selectivity toward DMC in the optimal conditions. It is worth noting that the catalyst can be easily separated by filtration and reused. A series of KF/Mg-Fe oxides were fabricated via the solid-state reaction between KF and Mg-Fe oxides. Especially, when 20 wt % KF was supported on the Mg-Fe bi-metal oxides and calcined at 400–600 °C, the solid material with more basic sites than the support itself was obtained. When applied as catalyst to dimethyl carbonate (DMC) synthesis through transesterification of ethylene carbonate (EC) and methanol, this material can afforded up to 88 % yield and 97 % selectivity toward DMC in 2 h under reflux conditions with the molar ratio of methanol to ethylene carbonate set at 8. It is worth noting that the catalyst was easily separated and reused, retaining at least 89 % catalytic activity during the first four recycles. Although an attenuated activity was still observed due to the inevitable filtration loss and dissolution, this solid base can still provide clues to the development recyclable catalyst in green synthesis of DMC.
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Biomedical Materials
·
2024
·Vol. 19
·期 2
·025018
·
IF 3.9
Antong Jiang,Teng Wang,Xiaoling Lu,Yuxiang Tian,Zihan Jiang,Bin Xu,Hanyuan Zhang,Weijun Fang
The application of both chemotherapy and ferrotherapy together has shown great potential in increasing the effectiveness of cancer treatment. To achieve such a combination, we herein have synthesized Fe3O4 core/MIL-100(Fe) shell nanocomposites (FM) that can be used for tumor chemo-ferroptosis combination therapy. In these nanocomposites, the anticancer drug 10-hydroxycamptothecin (HCPT) and iron ions could be co-delivered into tumors. On one hand, the released HCPT molecules can enter the cell nucleus and bind with DNA, resulting in induction of tumor cell apoptosis. On the other hand, the iron ions could react with H2O2 leading to the production of ROS through the Fenton reaction, thereby triggering tumor cell ferroptosis. Consequently, a superior antitumor effect was achieved through the combination of the apoptosis and ferroptosis. Additionally, the Fe3O4 core endowed FM with high performance for magnetic resonance imaging, which further provided novel avenues for imaging guidance therapy. Therefore, we anticipate that application of these nanocomposites could have great potential in the field of tumor therapy.
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Materials Today Bio
·
2025
·
IF 10.2
Xinying Liu,Baohui Liu,Conglong Chen,Chaowei Hong,Jia Xu,Yixuan Ruan,Ling Huang,Shanni Hong,Wei Chen,Ye Kuang
A significant challenge in modern radiotherapy (RT) is to minimize the detrimental effects on adjacent healthy tissues while concurrently increasing the susceptibility of tumor tissue to radiation. Investigating nanoradiosensitizers with multifunctional properties has a lot of potential as a highly effective strategy for augmenting the efficacy of RT. A novel Janus Ag/Fe-HfO 2 nanoparticle was synthesized in a single-step process. This versatile nanoradiosensitizer combines photothermal capabilities, enzyme-like activities, and the capacity for magnetic resonance imaging (MRI). The surfaces have been meticulously engineered with PEG to boost biocompatibility and adorned with RGD-targeting peptides that selectively target tumor cells (Ag/Fe-HfO 2 -PEG-RGD). The characterization results have demonstrated the successful preparation of Janus Ag/Fe-HfO 2 nanoparticles with a diameter of roughly 10 nm. Furthermore, the photothermal properties, MRI ability, and enzymatic catalytic activities (generate O 2 , produce hydroxyl radical, and consume GSH) of Ag/Fe-HfO 2 -PEG-RGD were verified in vitro experiments. In vivo experiments, by integrating T 1 -weighted MRI-guided RT with the enzymatic activities of these nanoparticles, along with the application of photothermal heating, we have achieved a synergistic enhancement in the therapeutic efficacy of RT. Moreover, it stimulates tumor-specific immune responses, leading to an increased presence of tumor-infiltrating CD8 + T cells. This integrated multimodal nanotherapeutic platform, which capitalizes on the potent enhancement of RT effects, offers a promising new strategy in the ongoing battle against cancer.
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Small
·
2025
·
IF 12.1
Jinyuan Zhang,Haifeng Liu,Jiajun Tian,Endong Hu,Xiujuan Gao,Haitao Hu,Zhengyou He,Kangli Wang,Kai Jiang,Hongwei Tao
Iron oxide (Fe 3 O 4 ) has attracted significant attention as a promising anode material for sodium-ion batteries (SIBs) due to its natural abundance, environmental benignity, and high theoretical capacity of 926 mA h g −1 . Nevertheless, its practical application is limited by intrinsic drawbacks, including low electrical conductivity, sluggish Na⁺ diffusion kinetics, and severe volume variation during cycling, leading to rapid capacity fading and poor rate capability. To address these issues, a novel Fe 3 O 4 /Fe@N-doped carbon (Fe 3 O 4 /Fe@CN) nanostructure is rationally designed, which integrates Fe 3 O 4 /Fe homogeneous heterojunctions with a uniform nitrogen-doped carbon shell. The built-in electric field at the Fe-Fe 3 O 4 interface promotes charge redistribution and accelerates electron/ion transport, while the N-doped carbon shell enhances electrical conductivity and buffers mechanical stress during sodiation/desodiation processes. Benefiting from this synergistic structure, the Fe 3 O 4 /Fe@CN anode delivers a high reversible capacity of 336.9 mA h g −1 at 0.1 A g −1 , excellent rate capability with 244.7 mA h g −1 at 2 A g −1 , and remarkable cycling stability, retaining 76.4% capacity after 500 cycles. Furthermore, a full cell assembled with a Na 3 V 2 (PO 4 ) 3 cathode exhibits a high energy density of 112.67 Wh·kg −1 at 51.42 W·kg −1 and outstanding cycling performance. This study offers a versatile strategy to unlock the potential of Fe 3 O 4 for high-performance SIB anodes through heterojunction and interfacial engineering.
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Advanced Composites and Hybrid Materials
·
2025
·Vol. 8
·期 4
·1-12
·
IF 21.8
Wang Lijuan,Shi Yaqin,Wang Yuan,Jia Chunijang,Hou Jie,Su Yizhen,Xu Ben Bin,Liao Zhijian,Zhu Linhua
Synergistic effect between M-N X sites and M X O Y particles in hierarchical porous M–N-C catalysts holds great promises in boosting oxygen reduction reaction (ORR). In this work, 1,4-dicyanobenzene was utilized as a molecular template to prepare the hierarchical porous Fe–N-C catalysts with size-tunable Fe 3 O 4 particles for enhanced ORR in Zn-air battery. The as-prepared Fe 3 O 4 #Fe–N/C DB0.1 owned a half-potential of 0.90 V vs RHE, exceeding that of commercial 20%Pt/C (E 1/2 = 0.82 V vs RHE), showing a maximum power density of 321 mW cm −2 in a homemade Zn-air battery. Density functional theory (DFT) calculations indicate that the electronic interaction between Fe 3 O 4 and Fe-N 4 sites enhances the adsorption energy of *OOH, effectively optimizing the energy barrier for *O formation, significantly reducing the limiting energy barrier. Such superior ORR activity in Fe 3 O 4 #Fe–N/C originated from the optimized hierarchical pores and synergistic effect between Fe-N X sites and Fe 3 O 4 particles. This work provides a new and facile template strategy for engineering hierarchical porous carbon-based materials to achieve highly efficient catalytic reactions.
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Nano Energy
·
2025
·
IF 17.1
Jiangxin Wang,Yuancheng Zhong,Xu Zhang,Xianfeng Xu,Minmin Liu,Kuanhong Mei,Kaixin Zhang,Weiguo Xu,Shuo Li
The efficient integration of photovoltaic conversion and energy storage technologies is critical to overcoming constraints in solar energy utilization. Solar rechargeable flow batteries (SRFBs) integrate solar energy conversion and storage via photoelectrode-driven redox processes, enabling economically viable pathways for sustainable solar energy storage. However, SRFB development faces limitations of thermodynamic voltage ceilings imposed by photoelectrode/redox couple energy level mismatches and the long-term durability of photoelectrodes. In this study, a PANI/BiVO 4 (PBVO) photoelectrode was fabricated, effectively preventing direct contact between BiVO 4 (BVO) and the electrolyte, thereby suppressing the photocorrosion issues. Meanwhile, [Fe(CN) 6 ] 3- /[Fe(CN) 6 ] 4- and Br - /Br 3- (Fe-Br) redox pairs with high redox reversibility were used in the SRFB system. The designed PBVO Fe-Br SRFB achieved ultra-long stability and a sustained photocurrent for up to 50 h. Furthermore, the effectiveness of the charge transfer pathway in the PBVO electrode within the Fe-Br SRFB was verified, providing insights into the design of SRFBs.
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DESALINATION
·
2025
·
IF 9.8
Pei Wang,Pu Li,Chencheng Dong,Chao Yang,Lin Lin,Xiao-yan Li
The integration of heterogenous Fenton reaction with membrane filtration has emerged as an effective technology for removing micropollutants from water. In this study, a novel bimetallic Fe Mo oxide (FeMoO)-modified catalytic ceramic membrane (CM) was fabricated, enabling continuous Fenton reaction for micropollutant removal and membrane fouling mitigation. By coating the FeMoO catalyst hybridized with NH 2 -MIL-88B(Fe) (NM88B) on the CM, i.e., FeMoO/NM88B@CM, a catalytic layer ~24 μm in thickness was formed on the membrane to provide abundant active sites for H 2 O 2 activation during the filtration process. FeMoO/NM88B@CM with H 2 O 2 dosing exhibited a remarkable treatment performance, achieving 98.5 % degradation of moxifloxacin (MOX) within 3.1 min of single-pass water filtration, greatly surpassing the 16.8 % removal by FeMoO/NM88B@CM without H 2 O 2 dosing and 16.2 % removal by bare CM with H 2 O 2 dosing. The FeMoO/NM88B@CM/H 2 O 2 system also performed exceptionally well in treating actual secondary wastewater effluent, removing more than 60 % of the residual organics while mitigating the membrane fouling problem. In addition, the catalytic membrane filtration demonstrated its high effectiveness in degrading various micropollutants, in the presence of complex water matrix substances, and during long-term operation. Hydroxyl (‧OH) and superoxide (‧O 2 − ) radicals were identified as the active species generated by the catalytic membrane for organic oxidation and membrane fouling control. It is considered that H 2 O 2 -induced Mo(VI)/Mo(IV) cycle of the immobilized Fe Mo bimetallic catalyst played a crucial role in driving the essential Fe(II)/Fe(III) redox cycle for continuous regeneration of Fe(II) and heterogeneous Fenton oxidation. The research findings provide valuable insights into the fabrication and potent functionality of catalytic ceramic membranes in high-rate removal of micropollutants for water pollution control.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Rongrong Mu,Wenhui Song,Zili Li,Yuting Pan,Jingwei Liu,Fengyu Qu,Huiming Lin
Both sonodynamic therapy (SDT) and nanozymes can be considered specialized forms of catalysis, which are related to the electron structure. In this work, Fe doping was employed to introduce electronic localization and spin polarization toward porous MoO 2 nanospheres to improve the anticancer catalytic efficiency. All the Fe atoms are single-distributed to substitute for some lattice positions of Mo. Compared with MoO 2 @PEG, MoO 2 /Fe@PEG results in a 2.8-fold increase in ROS generation, which is attributed to spin polarization. This phenomenon enhances charge separation, increases conductivity, and promotes O₂ adsorption, thereby significantly improving the ROS production efficiency. Furthermore, MoO 2 /Fe@PEG also has superior mimic-catalase (CAT) activity (318,467 U g −1 ), which is even greater than that of natural catalase (220,834 U g −1 ). Compare with MoO 2 @PEG Fe doping increased the activity by 76.0 times because electron localization can decrease the free energy of the redox reaction. This novel CAT ability can convert endogenous H 2 O 2 into O 2 , alleviating tumor hypoxia and increasing ROS production. Notably, MoO₂/Fe@PEG also mimics GSH oxidase and NADPH oxidase (NOX) activities to consume GSH and restrain its regeneration at the same time, contributing to oxidative stress. The synergistic effects of SDT and multiple enzymes not only exhibit potent tumor inhibition but also elicit a robust immune response to prevent metastasis and recurrence.
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