JOURNAL OF ALLOYS AND COMPOUNDS
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2026
·
IF 6.7
Yanzhi Cai,Xue Huang,Laifei Cheng,Yalong Chai,Zixuan Yu,Mingxing Chen,Shaoxiong Ren,Jiaoe Dang
Achieving self-supporting superflexible binder-free composites where all components serve simultaneously as structural backbones and microwave-absorbers is a technical challenge. This study successfully combined several microwave absorbing materials, including Fe 3 O 4 , NiCo-MOF derivatives, and CNTs, into a binder-free self-supporting superflexible Buckypaper in one step through directional pressure filtration. Fe 3 O 4 -CoNi-MOF was in-situ grown on a single CNT to form a magnetic MOF-coated CNT (CNT@MOF), which was then subjected to high-temperature carbonization to obtain a magnetic MOF-derived carbon-coated CNT (CNT@Fe 3 O 4 /CoNi-C). The combination of Fe₃O₄/CoNi-MOF and CNTs simultaneously promotes magnetic loss and dielectric loss, thereby significantly enhancing impedance matching and electromagnetic energy attenuation capabilities. The optimal carbonization temperature for the CNT@Fe 3 O 4 /CoNi-C Buckypaper is 700 ℃, at which the minimum reflection loss (RL min ) is −58.12 dB and the absorption bandwidth is 5.02 GHz. The interweaving of CNTs forms a robust yet superflexible skeleton, while the in-situ growth of Fe₃O₄/CoNi-MOF derivatives on a single CNT enhances the structural stability of the skeleton. The Buckypaper remains intact after repeated 2 mm-radius curling, knotting, 180° bending. Therefore, this study presents new insights into the preparation of self-supporting, superflexible MOF-derived microwave absorption materials.
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高影响因子
WATER RESEARCH
·
2026
·
IF 12.8
Ping Zhang,Chenchen Zhao,Fei Jiang,Chuyang Wu,Tianqi Wang,Xing Xu,Mengjie Wu,Zhanli Chen,Youqin Zou
Green Fenton-like reactions based on monometallic single-atom dual-reaction-center systems have emerged as promising strategies for sustainable water purification owing to their oxidant-free operation and low energy demand. However, their practical deployment is often hindered by limited degradation kinetics and unresolved mechanisms. Here, we report a carbon nitride-supported Fe/Mn bimetallic catalyst composed of Fe nanoclusters and adjacent Mn single atoms (FeMn-CN) that enables ultrafast and self-sustaining pollutant degradation under oxidant-free conditions. The catalyst achieves 99.5% removal of bisphenol A (BPA) within 3 min, setting an ultrahigh rate to date among self-sustaining water purification systems. Combined experimental investigations and density functional theory calculations reveal that the reaction proceeds predominantly via a direct electron-transfer pathway. Fe nanoclusters serve as primary electron acceptors, extracting electrons from BPA without external oxidants, while adjacent Mn single atoms coordinated in Mn-N 4 sites synergistically enhance the electron-accepting capacity of Fe and substantially lower the charge-transfer energy barrier. This atomic-level cooperation endows FeMn-CN with exceptional activity across a broad pH range (pH 2-10), strong tolerance to complex water matrices, high selectivity toward electron-rich contaminants and facile regeneration. Furthermore, continuous-flow reactor tests and life-cycle assessment collectively verify the scalability and superior environmental sustainability of the FeMn-CN process. This work establishes an atomic-level design principle for electron-transfer-dominated self-sustaining remediation materials, advancing the development of next-generation oxidant-free water purification technologies.
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Small
·
2026
·
IF 11.8
Hang Zhang,Yinuo Wu,Zhen Zhang,Ying Hou,Peizhi Liu,Ting Liao,Bingshe Xu,Yanhui Song,Haixia Zhang,Junjie Guo,Ziqi Sun
M-N-C single-atom catalysts have been demonstrated to be a promising class of non-noble-metal based catalysts, but their activity is largely constrained by the symmetrical electronic density distribution of the M-N 4 moieties. Herein, a ZIF-8 derived Fe/Fe dual-center catalyst (FeN 4 /FeO 5 @NC) is constructed by introducing a O-FeO 4 configuration adjacent to the Fe-N 4 sites to form asymmetric dumbbell-shaped FeN 4 -O-FeO 4 active sites, resulting in improved intrinsic activity of Fe─N─C catalyst. The dumbbell FeN 4 -O-FeO 4 dual-center catalyst features an electron transfer pathway of “FeN 4 → bridged O → FeO 4 ”, which breaks the symmetry of the electronic density distribution of the Fe moiety and regulates the position of the d-band center, increasing the electron transfer efficiency, reducing the desorption energy barrier of the rate-determining step, and enhancing the activation ability of O 2 molecules. The obtained FeN 4 -O-FeO 4 dual-center catalyst exhibits excellent ORR performance in a pH-universal range. The liquid-state Zn-air battery (ZAB) with this FeN 4 -O-FeO 4 dual-center catalyst delivers an outstanding open circuit voltage of 1.502 V and a peak power density of 246 mW cm −2 , superior to the Pt/C-cathode ZAB. This work represents an exploration of ways to improve the ORR performance of Fe─N─C catalysts and provides a paradigm for rationally designing low-cost, highly catalytic, and stable non-noble metal catalysts.
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高影响因子
MOLECULES
·
2024
·Vol. 29
·期 4
·850
·
IF 4.2
Meng Guo,Dou Wu,Hongyu Yang,Xiao Zhang,Dong-Xu Xue,Weiqiang Zhang
The use of gaseous CO in Pd-catalyzed carbonylative quinolone synthesis presents challenges related to safety and precise pressure control. In response, a streamlined non-gaseous synthesis of 4-quinolone compounds has been developed. This study introduces a tunable CO-releasing system utilizing Fe(CO)5activated by a dual-base system of piperazine and triethylamine. This alternative liquid CO resource facilitates the palladium-catalyzed carbonylative C-C coupling and subsequent intramolecular cyclization. By tuning the tandem kinetics of carbonylation and cyclization, this non-gaseous method achieves the successful synthesis of 22 distinct 4-quinolones with excellent yields. This is achieved through the three-component condensation of sub-stoichiometric amounts of Fe(CO)5with 2-iodoaniline and terminal alkynes. Operando mechanistic studies have revealed a novel CO transfer mechanism that facilitates homogeneous carbonylative cyclization, distinguishing this method from traditional techniques. In addition to addressing safety concerns, this approach also provides precise control over selectivity, with significant implications for pharmaceutical research and the efficient synthesis of pharmaceutical and bioactive compounds.
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CHEMICAL ENGINEERING JOURNAL
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2026
·
IF 12.5
Xiaoqiang Li,Xiaorui Zhang,Xin Zhang,Shengjun Wen,Xiaoxiao Duan,Yongsheng Ren
2-Mercaptobenzothiazole (MBT), a highly toxic industrial corrosion inhibitor containing a thiol group, poses severe threats to ecological and human health. In this study, a trimetallic cathode (FeCoMn@LNC-500) was fabricated by in situ growing oxygen-vacancy-rich FeCoMn-LDHs on carbon paper followed by carbonization at 500 °C. FeCoMn@LNC-500 exhibited a cylindrical fiber-rod structure decorated with numerous densely aggregated spherical particles, which increased the electrochemical active surface area and reduced the charge-transfer resistance. Under optimal conditions, FeCoMn@LNC-500/EF achieves a degradation rate of 100% within 70 min through singlet oxygen ( 1 O₂) mediated non-radical oxidation (k = 0.0557 min −1 ). The removal efficiency achieved with this cathode was approximately 11.8, 5.0, 2.0, and 3.2 times higher than those of the PC-500, FeMn@LNC-500, CoMn@LNC-500, and CoFe@LNC-500 cathode systems, respectively. The outstanding degradation performance is primarily attributed to the carbon paper's excellent conductivity, which enhances the in-situ synergistic cycling of Co, Fe, and Mn to accelerate the Fenton reaction while also improving system stability, as demonstrated by a 7-cycle operational test and the detection of extremely low metal-ion leaching. Quenching experiments and electron paramagnetic resonance (EPR) spectroscopy confirmed that the non-radical 1 O₂ played a dominant role in the oxidation process. HPLC-MS analysis revealed the degradation mechanism and pathway of MBT: non-radical-dominated selective cleavage of the S N bond followed by stepwise mineralization. The carbon-paper-based cathode developed in this work provides insights into the electro-Fenton degradation of thiol-containing wastewater and is expected to offer a new strategy for the efficient treatment of coal-chemical pipeline wastewater.
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JOURNAL OF NANOPARTICLE RESEARCH
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2026
·Vol. 28
·期 3
·82
·
IF 3.5
Zhao Xu,Guo Hongyan,Zhang Nannan,Yue Zhi,Gu Xungang
A novel dual Z-scheme BiOBr/NH 2 -MIL-101(Fe)/g-C 3 N 4 (BNG) heterojunction was constructed via a simple two-step solvothermal process. NH 2 -MIL-101(Fe) nanoparticles and BiOBr microspheres were uniformly deposited on the surface of g-C 3 N 4 . The prepared BNG exhibited significantly enhanced photocatalytic performance for tetracycline (TC) degradation compared to single catalyst. The optimized BNG-19 composite (with 19% NH 2 -MIL-101(Fe)/g-C 3 N 4 ) achieved 92.38% degradation of TC within 75 min under visible light, which was 2.47, 1.78, and 1.84 times higher than that of pure g-C 3 N 4 , NH 2 -MIL-101(Fe), and BiOBr, respectively. Moreover, the composite exhibited excellent stability with 82.4% removal efficiency after five cycles. The enhanced photocatalytic performance was attributed to the synergistic dual Z-scheme charge transfer mechanism, which was directly evidenced by in-situ irradiated XPS showing opposite directional shifts of Bi 4f (positive) and Fe 2p/N 1s (negative). This unique charge transfer pathway effectively promoted the separation of photogenerated carriers, with •OH and •O 2 ⁻ identified as the dominant reactive species. This work provides a new strategy for constructing g-C 3 N 4 -based dual Z-scheme heterostructures with direct mechanistic evidence for efficient environmental remediation.
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Nano-Micro Letters
·
2026
·Vol. 18
·期 1
·237
·
IF 38.5
Wang Xiaoxue,Xu Yuhui,Zhang Jianhua,Xi Yukun,Hou Ningjing,Chen Yixuan,Liu Dongzhu,Yang Zihao,Wen Haocheng,Kang Jia,Yang Xiaoli,Song Xuexia,Wang Jingjing,Li Wenbin,Zhang Jiujun,Zhang Kun,Li Xifei
Na4Fe3(PO4)2P2O7 (NFPP) is regarded as a prospective cathode for sodium-ion batteries (SIBs) because of its high structural stability and cost-effectiveness. However, its practical application is hindered by intrinsically low electronic conductivity. Herein, an unconventional electron transfer mechanism from Ni2+ to Fe3+ ions is unveiled in Ni-doped Na4.3Fe3(PO4)2P2O7 (NFPP-Ni) cathode, which facilitates electronic coupling within the Fe−O−Ni coordination unit and thereby effectively boosts electron transport. Moreover, the redox kinetics and reversibility of NFPP materials are predominantly governed by the degree of Fe−O covalency. The intermediate eg occupancy of Fe2+, modulated by the presence of Ni2+, optimizes the overlap between Fe d and O p orbitals. The adjustment of Ni dopant strikes a balance between accelerating Na+ diffusion kinetics and mitigating lattice strain during cycling. As a result, the NFPP-Ni electrode displays impressive rate capacity (121.0 mAh g−1 at 0.1C / 80.9 mAh g−1 at 10C) and stable cyclability (89.1% capacity retention after 1000 cycles). More importantly, the relationship between Fe eg orbital occupancy and Fe−O covalency in NFPP as modulated by various transition metal cations (Ni2+, Mn2+, Zn2+, Co2+ and Cu2+) with different electron configurations are systematically elucidated, thereby providing insights for the commercial development of sodium-ion batteries (SIBs).
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高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2022
·
IF 5.518
Ying Ji,Honglei Liu,Yujiao Guo,Junming Guo,Mingwu Xiang,Wei Bai,Xiaofang Liu,Hongli Bai
At high current density, low capacity and rapid capacity decay of spinel LiMn 2 O 4 cathode material during the cycle limit its application. Herein, element doping approach to restrain Jahn-teller effect combined with crystal plane regulation to mitigate Mn dissolution is employed to synthesize a series of truncated octahedron LiNi 0.02 Fe x Mn 1.98−x O 4 (x ≤ 0.12) which provide high exposure {111} surfaces as well as a small portion of {110} and {100} facets for offering Li + ion rapid diffusion channel. Many characterizations such as XRD , SEM and TEM show that Ni-Fe co-doped can effectively promote the development of crystal and the preferential growth of crystals planes. Electrochemical test results imply that at 1 C the difference between capacity and capacity retention ratio in terms of LiNi 0.02 Mn 1.98 O 4 (LNMO) and Ni-Fe co-doping samples are not obvious. With the increasing of current densities, Ni-Fe co-doping samples exceptional rate capability and cycle stability become apparent. The optimal LiNi 0.02 Fe 0.05 Mn 1.93 O 4 (LNFMO-5) and LNMO can keep 76.9% and 74.6% of their original capacity of 113.4 mAh·g ‐1 as well as 116.2 mAh·g ‐1 after 500 cycles at 1 C, respectively. At 10 C, the LNFMO-5 sample delivers the capacity of 89.3 mAh·g ‐1 and a higher capacity retention ratio of 72.9% after 2000 cycles, while the LNMO sample is only 63 mAh·g ‐1 and 67.2%. Even at 20 C, The LNFMO-5 sample still reaches a high specific capacity of 84.9 mAh·g ‐1 and a higher capacity retention ratio of 76.1% after 2000 cycles, which are much higher than the LNMO sample (63.0 mAh·g ‐1 ) and 57.4% capacity retention rate. CV and EIS analysis manifest that the LNFMO-5 has a higher D Li + and a lower E a than that of the LNMO. A unique Ni-Fe co-doped truncated octahedral LiMn 2 O 4 material with exceptional electrochemical property will be an attractive candidate for the preparation high-performance and long-cycle spinel LiMn 2 O 4 cathode materials.
研究领域:
材料科学
·
电化学
·
储能技术
·
锂离子电池
·
正极材料
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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2018
·Vol. 43
·期 32
·15358-15364
·
IF 4.229
Qiang Wu,Cheng Ji,Xiaohui Zhang,Qichang Pan,Jiujun Zhang,Qingyu Li,Hongqiang Wang
Core-shell Fe 3 O 4 @Fe nanoparticles embedded into porous N-doped carbon nanosheets was prepared by a facile method with NaCl as hard-template. The three-dimensional carbon architecture built by carbon nanosheets enhance the conductivity of the encapsulated Fe 3 O 4 @Fe nanoparticles and strengthen the structure stability suffering from volume expansion during extraction and insertion of lithium ions . Rich Pores enhance the surface between electrode and electrolyte, which short the transmission path of ions and electrons. The core-shell structure with Fe as core further improves charge transferring inside particles thus lead to high capacity. The as-prepared Fe 3 O 4 @Fe/NC composite displays an irreversible discharge capacity of 839 mAh g −1 at 1 A g −1 , long cycling life (722.2 mAh g −1 after 500th cycle at 2 A g −1 ) and excellent rate performance (1164.2 and 649.2 mAh g −1 at 1 and 20 A g −1 , respectively). The outstanding electrochemical performance of the Fe 3 O 4 @Fe/NC composite indicates its application potential as anode material for LIBs .
研究领域:
材料科学
·
电化学
·
储能
·
纳米材料
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KOREAN JOURNAL OF CHEMICAL ENGINEERING
·
2022
·Vol. 39
·期 12
·3305-3314
·
IF 3.146
Liu Zhihao,Qiu Kui,Dong Yu,Jin Zhaobo,Liu Luwei,Wu Jirong
A non-aqueous phase (Sb/Fe/NMP) desulfurization system for the removal of hydrogen sulfide from natural gas was constructed by introducing SbCl 3 and FeCl 3 in a specific ratio into N-methylpyrrolidone (NMP). The desulfurizing agent and its sulfur product were characterized, and the absorption pattern of H 2 S by the system was investigated by static desulfurization experiments. The results indicate that the desulfurizer’s sulfur capacity can reach 16 g/L at room temperature and pressure, and that adding the optimum amount of water and appropriate temperature increase can assist to increase desulfurization efficiency. The system maintained a sulfur capacity level of more than 90% of the initial sulfur capacity after five consecutive desulfurization-regeneration cycles. XRD and XPS spectrogram revealed that the regenerated solid product was high purity sulfur. Sb 3+ is a key component to ensure the effective absorption of H 2 S. The presence of a moderate amount of Fe 3+ can oxidize and absorb small amounts of H 2 S and promote the oxidative regeneration of the system. In addition, we combined the obtained experimental data with density flooding theory (DFT) theoretical calculations to show that the effective coordination of Sb(III) with HS − in the NMP environment is the main reason for the effective absorption of H 2 S by the desulfurizer. NMP is not involved in the coordination absorption process of hydrogen sulfide.
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高影响因子
PROCESS SAFETY AND ENVIRONMENTAL PROTECTION
·
2022
·
IF 7.926
Miao Jiang,Kun Wang,Ruiyuan Xue,Qingliang Zhao,Long Wang,Weiye Wang,Jing Ding
Antimony (Sb) finds its wide application in industries, however, the research on Sb solidification/stabilization (S/S) in the Sb-contaminated soil is currently insufficient, particularly in seasonal freezing regions. Here six composite materials of Fe/Fe 2+ -fly ash-concrete additive (Fe-FA-CA) were employed and optimized to remediate the Sb-contaminated soil subject to 40 freezing-thawing (F-T) cycles. After remediation, FeSO 4 -fly ash-calcium lignosulfonate (FFC) exhibited the best resistance performance to F-T. The stabilization efficiency was evaluated with TCLP at 92.92%. Meanwhile, Sb concentration met the criteria of landfill for inert waste assessed with the compliance test for leaching (CT) of European Standard . The S/S efficiency of Sb dropped slightly from 92.68% to 88.22% (TCLP) and from 97.18% to 93.37% (CT), respectively, after aging 40 F-T cycles. The fraction of residual Sb in the soil treated by FFC was increased by 10.41%, and the strength of the S/S soil was much higher than 350 kPa, the requirement of landfills in the U.S. during F-T cycles. Additionally, the poorly crystalline Fe in the soil remediated by FFC was increased by 4.54 g/kg, suppressing Sb migration. The feasibility and effectiveness of FFC in S/S of Sb demonstrated its potential to remediate Sb-contaminated soil in seasonal freezing regions.
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高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Xiyang Kang,Ziqian Jin,Huaiqi Peng,Zihao Cheng,Lijie Liu,Xin Li,Lixia Xie,Jianmin Zhang,Yutao Dong
Lithium-sulfur (Li-S) batteries are currently only in the basic research stage and have not been commercialized, which is mainly affected by the poor conductivity of sulfur/lithium sulfide (S/Li 2 S), volume expansion effect of sulfur and the shuttle effect of lithium polysulfides (LiPSs). Herein, a three dimensional (3D) carbon nanotubes (CNTs) decorated cubic Co 9 Se 8−x /FeSe 2−y (0 ＜ x ＜ 8, 0 ＜ y ＜ 2) composite (Co 9 Se 8−x /FeSe 2−y @CNTs) is developed, and used as the functionalized mediator on polypropylene (PP) in Li-S batteries. Benefiting from the good electrical conductivity, large number of Se vacancies and the triple block/adsorption/catalytic effects of Co 9 Se 8−x /FeSe 2−y @CNTs, the cell with Co 9 Se 8−x /FeSe 2−y @CNTs//PP modified separator delivers a high reversible capacity (1103.5 mA h g −1 ) at 1C after three cycles activation at 0.5C and remains 446 mA g h −1 after 750 cycles with a 0.08% capacity decay rate each cycle. Moreover, at 0.2C, a high areal capacity of 3.63 mA h cm −2 after 100 cycles with a high sulfur loading of 4.1 mg cm −2 is obtained. The in-situ XRD tests revealing the transition path of α -S 8 → Li 2 S → β -S 8 during the first charge–discharge process, then β -S 8 → Li 2 S → β -S 8 conversion reaction in the next cycles, and firstly determine the sulfur-selenide active intermediates (Se 1.1 S 6.9 ) during cycles. The work provides a new insight into the development of bimetallic selenide composites by defect engineering with highly adsorptive and catalytic properties for Li-S batteries.
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高影响因子
危险品化学品经营许可证（带存储）