ACS Nano
·
2021
·
IF 15.881
Shaoda Huang,Shuanglong Lu,Shun Gong,Qiuju Zhang,Fang Duan,Han Zhu,Hongwei Gu,Weifu Dong,Mingliang Du
Engineering the morphology and electronic properties simultaneously of emerging metallene materials is an effective strategy for enhancing their performance as oxygen reduction reaction (ORR) electrocatalysts. Herein, a highly efficient and stable ORR electrocatalyst, Fe-doped ultrathin porous Pd metallene (Fe–Pd UPM) composed of a few layers of 2D atomic metallene layers, was synthesized using a simple one pot wet-chemical method and characterized. Fe–Pd UPM was measured to have enhanced ORR activity compared to undoped Pd metallene. Fe–Pd UPM exhibits a mass activity of 0.736 A mgPd–1 with a loss of mass activity of only 5.1% after 10 000 cycles at 0.9 V versus the reversible hydrogen electrode (vs RHE) in 0.1 M KOH solution. Density functional theory (DFT) calculations reveal that the stable Fe dopant in the inner atomic layers of Fe–Pd UPM delivers a much smaller overpotential during O* hydrogenation into OH*. The morphology, porous structure, and Fe doping were verified to have enhanced ORR activity. We believe that the rational design of metallene materials with porous structures and interlayer doping is promising for the development of efficient and stable electrocatalysts.
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DOI
PubMed
高影响因子
RSC Advances
·
2017
·Vol. 7
·期 73
·46215-46220
·
IF 3.108
Youzhi Wang,Yurun Feng,Xue Guo,Yu Liu,Hongyu Gong
Fe-doped polymer-derived SiCN ceramics were synthesized by a precursor conversion method with different contents of nano-Fe2O3. The phase composition and microstructure were characterized by XRD, SEM and TEM. The results revealed that α-Fe and graphite phases were generated during the synthetic process. The electromagnetic and wave absorbing properties of the Fe-doped SiCN ceramics were analyzed with different amounts of nano-F2O3 over the frequency range of 2–18 GHz. The existence of α-Fe and graphite phases improved the electromagnetic properties of the materials greatly. The reflectance and electromagnetic attenuation coefficient of Fe-doped SiCN ceramics (15 wt% F2O3) reached −11 dB and 325 at 10.5 GHz, respectively, which indicated that the Fe-doped SiCN ceramics possessed excellent absorbing properties.
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DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2016
·
IF 3.299
Meichao Gao,Dafeng Zhang,Xipeng Pu,Hong Li,Wenzhi Li,Xin Shao,Dongdong Lv,Bingbing Zhang,Jianmin Dou
Fe-doped BiOCl photocatalysts were synthesized by a simple combustion method. The as-synthesized catalysts were characterized by X-ray diffraction, scanning electron microscope, transmission electron microscope, X-ray photoelectron spectroscopy and UV–Vis diffuse reflectance spectroscopy. Fe 3+ doping leads to red-shift in the absorption band and increased visible light absorption. The photocatalytic reaction tests in the degradation of the dyes of rhodamine showed that the doping of Fe 3+ could bring about a big increase in the photocatalytic activity under visible light irradiation. The main reactive oxygen species and photocatalytic mechanism of Fe-doped BiOCl under visible light irradiation were discussed in detail.
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DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2019
·Vol. 30
·期 15
·14573-14579
·
IF 2.195
Teng Zhen,Zeng Sifan,Feng Wanlin,Zhu Lini,Tan Yongqiang,Han Xiaochun,Chen Chen,Zhang Haibin
Fe-Fe 3 C@C composites are successfully synthesized via a facile pyrolysis process. Experimental results indicate that Fe-Fe 3 C nanoparticles are closely parceled among amorphous carbon and exhibit a core–shell structure. The obtained materials display excellent microwave absorption performance with an optimal reflection loss of − 35.6 dB at 17.2 GHz, and an effective absorbing bandwidth of 4 GHz (from 12.4 to 16.4 GHz) with the coating thickness of 2 mm. The magnetic loss derived from Fe core and dielectric loss on carbon materials as well as a good impedance matching are believed to play decisive roles for this favorable microwave absorbing properties. The composites are considered to be good candidates for microwave absorption applications.
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DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Yan Huang,Bowen Zang,Chang Zhang,Mingliang Xiang,Peng Xiao,Juntao Huo,Meng Gao,Rie Umetsu,Min Ji,Bingnan Yao,Yan Zhang,Yaocen Wang,Junqiang Wang
Coating soft magnetic powders by an insulation layer is an effective way to improve the high-frequency performance of soft magnetic powder cores. The quality of insulation coating is highly dependent of the coating materials and the coating method. In the present work, a commercial amorphous powder (Fe 73 Si 11 B 11 C 3 Cr 2 ) was primarily coated by a PDA/PEI layer by a co-deposition method in alkaline solution. A thick PDA/PEI layer with good homogeneity was co-deposited on the surface of amorphous soft magnetic powders. The high frequency core loss of magnetic powder cores was reduced by up to ~ 44 % at the magnetic induction of 0.1 T and the frequency of 100 kHz by primarily coating the amorphous powders by PDA/PEI. Microscopic images showed that the PDA/PEI coating layer on the amorphous powders does not peel off while being compressed. These results indicates that PDA/PEI insulation coating is a coating method which can effectively improve the comprehensive magnetic properties of magnetic powder cores.
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DOI
高影响因子
ACS Omega
·
2019
·
IF 2.584
Jinjuan Xue,Zhengrong Zhu,Yuqing Zong,Chengjuan Huang,Mingxin Wang
This study investigates the degradation of dimethyl phthalate (DMP) with hydrogen peroxide and ferrate (Fe(VI)) under various reaction conditions. The results showed that the optimum conditions for dimethyl phthalate removal from water were as follows: (a) pH 7.0 and (b) the original molar ratio of [Fe(VI)]/[H2O2]/[DMP] equal to 10:2:1. Under the optimum conditions, the degradation rate of DMP can reach 89.7% in 360 min. Furthermore, 2,5-dihydroxybenzaldehyde, isophthalic acid, 2-ethylhexanol, oxalic acid, 2,6-dihydroxybenzoic acid, 2,6-dihydroxybenzaldehyde, 2,5-dihydroxybenzoic acid, and monomethyl phthalate were identified as the degradation intermediates, and degradation pathways were proposed.
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DOI
高影响因子
Journal of Water Process Engineering
·
2025
·
IF 6.7
Xiao Han,Hao Huang,Junze Wang,Min Zhang,Haixia Wu
To address the environmental residues of tetracycline (TC) antibiotics and the spread of antibiotic resistance genes, as well as to develop efficient synergistic photocatalytic Fenton catalysts, this study synthesized iron-doped molybdenum disulfide (Fe-MoS 2 ) composite catalysts via a hydrothermal method and constructed a synergistic photocatalytic Fenton system for efficient TC degradation. Experimental results showed that the doping of iron significantly optimized the electronic structure of MoS 2 , reducing its bandgap from 1.51 eV to 1.30 eV, thereby broadening its light absorption range. Additionally, Fe Mo dual active sites suppressed charge recombination and improved charge separation efficiency. Under visible light irradiation, Fe-MoS 2 synergistically activated H 2 O 2 , achieving a TC removal rate of 82.3 % within 60 min. Iron doping promoted the heterogeneous Fenton reaction, accelerated the Fe 3+ /Fe 2+ cycling, and facilitated the direct reduction of H 2 O 2 by photogenerated electrons to produce active species ( O 2 − and 1 O 2 ), while the synergistic hole oxidation effectively degraded TC. Fe-MoS 2 exhibited excellent stability in weakly acidic to neutral environments as well as in complex aqueous matrices, along with good recyclability. This study provides new insights for the development of efficient bifunctional catalytic materials and offers significant reference value for the treatment of antibiotic contamination in real wastewater.
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产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
·
IF 6.3
Ruifeng Xu,Ke Wang,Jiaxin Liu,Zhongkang Cao,Wenbo Wang,Xu Zhang,Bingjun Yang,Juan Yang,Xianfeng Fan,Tongtong Yu,Pengjun Ma
The replacement of the oxygen evolution reaction (OER) with the urea oxidation reaction (UOR) coupled with the hydrogen evolution reaction (HER) in water electrolysis systems is regarded as a highly promising strategy for reducing hydrogen production energy consumption, enhancing hydrogen efficiency, and even effectively treating urea wastewater. However, the design and fabrication of UOR catalysts in the UOR coupled HER catalytic water electrolysis system remains one of the significant challenges. Herein, we employed a facile, operable, and practical solid-state reaction method to synthesize two representative types of transition metal phosphosulfide (MPS 3 ) catalysts, and the intrinsic and structural characteristics of these catalysts were systematically characterized. Subsequently, the MPS 3 catalyst was deposited onto a nickel foam substrate (NF) to obtain the MPS/NF catalytic electrode. The UOR and OER performance of the MPS 3 /NF catalytic electrode was evaluated to elucidate the competitive mechanisms of UOR and OER within the MPS 3 catalyst. Results indicated that the UOR driving potentials required for NiPS 3 /NF and FePS 3 /NF electrodes were individually reduced by 101 mV and 33 mV compared to the corresponding OER driving potentials under the condition of 100 mA/cm 2 , and NiPS 3 /NF and FePS 3 /NF electrodes could even achieve large UOR current density of 300 mA/cm 2 at potentials as low as 1.630 V (vs. RHE) and 1.647 V (vs. RHE), respectively. In-situ Raman spectroscopy combined with XPS analysis revealed distinct catalytic pathways for NiPS 3 and FePS 3 . During catalysis, NiPS 3 undergoes surface reconstruction to form γ-NiOOH, which exhibited superior selectivity toward urea oxidation, whereas FePS 3 predominantly generated β-FeOOH, whose activity was compromised by competing oxygen evolution, thereby conferring weaker UOR selectivity compared with NiPS 3 . For the UOR-coupled HER whole-cell urea electrolysis assessment, the NiPS 3 /NF and FePS 3 /NF whole-cell attained urea degradation efficiencies of 89.04 % and 69.61 %, respectively. This work provided a novel strategy and practical approach for the development of novel, efficient, and cost-effective MPS 3 catalysts for UOR coupled with HER in the treatment of urea wastewater for synergistic hydrogen production.
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产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2025
·Vol. 36
·期 25
·1-15
·
IF 2.8
Yan Yuefeng,Cheng Ziyan,Ma Guansheng,Chen Tao,Gao Boshi,Liu Yuhao,Huang Xiaoxiao
Reduced Graphene Oxide (RGO) has been proved to be a promising electromagnetic wave absorption (EMWA) material candidate owing to its superior electrical and dielectric properties, along with rich potential for structural design. However, the complicated synthesis process and the contradiction between impedance matching and attenuation capacity have hindered the further development and application of graphene-based absorbing materials. Herein, a Fe nanoparticle/RGO composites was synthesized through a facile in-situ chemical reduction process. The configuration of Fe nanoparticles regulates the permittivity and permeability of RGO and balances the impedance matching. The dipole polarization caused by the residual oxygen-containing functional groups in RGO, coupled with the interfacial polarization loss caused by the Fe/RGO interface, enhance the dielectric loss capacity, contributing to microwave loss in the high-frequency range. The natural resonance and exchange resonance caused by the nano Fe particles enhance the microwave loss capacity in the low-frequency range. Benefitting from the synergistic enhancement from dielectric loss and magnetic loss, Fe/RGO composites exhibit the characteristic of daul-band absorption. Notably, the sample FG-0.25 achieved an effective absorption bandwidth ( EAB ) of 5.33 GHz and a minimum reflection loss ( RL min ) of −48.9 dB. The absorption peaks in the low-frequency band can encompass a significant portion of the C-band. This research provides unique insights for the advancement of environmentally friendly and energy-efficient RGO based EMWA materials.
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产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2017
·Vol. 29
·期 4
·2733-2742
·
IF 2.019
Hou Huilin,Wang Lin,Yang Weiyou,Gao Fengmei
Fe-doped TiO 2 nanofibers with a thoroughly mesoporous structure were prepared via a facile foaming-assisted electrospinning method. The foaming agents and FeAcAc were introduced in the raw materials to create the mesopores and incorporate the Fe dopants into the conventional solid TiO 2 nanofibers, respectively, which could be accomplished simultaneously over a one-step calcination process. The photocatalytic experimental results demonstrate that the mesoporous Fe-doped TiO 2 nanofibers exhibit significantly enhanced activity toward the RhB degradation and splitting water for hydrogen generation under visible-light illumination, as compared to those of Fe-doped solid and intrinsic thoroughly mesoporous counterparts. The photocatalytic mechanism is proposed that the one-dimensional mesoporous nanostructure can enhance the transportation of the reactant and products, and the Fe-doping induces the shift of the absorption edge into the visible-light range and restrains the recombination of photo-generated electrons and holes, which can synergistically improve their activity.
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DOI
高影响因子
CHINESE JOURNAL OF CHEMICAL ENGINEERING
·
2024
·
IF 3.7
Jianfang Liu,Hongwei Huang,Jie Yang,Laishuan Liu,Yu Li
A series of Au/Co x Fe 3- x O 4 catalysts was synthesized using the sol-deposition method by depositing 2–5 nm Au particles on Fe-doped Co 3 O 4 . Co 2 FeO 4 , with a Co/Fe molar ratio of 2:1, exhibited higher specific surface area , Co 3+ /Co 2+ ratio, and oxygen vacancy content compared to Co 3 O 4 . As a result, it displayed better performance in CO oxidation , achieving a total conversion temperature ( T 100 ) of 96 °C. Au greatly improved the catalytic efficiency of all Co x Fe 3- x O 4 samples, with the 0.2%Au/Co 2 FeO 4 catalyst achieving a further decrease in T 100 to 73 °C. Stability tests conducted at room temperature on the 1%Au/Co x Fe 3- x O 4 catalysts demonstrated a slowed deactivation rate after Fe-doping. The reaction pathway for CO oxidation catalyzed by Au/Co 2 FeO 4 followed the Mars-van Krevelen mechanism.
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DOI
高影响因子
Journal of Water Process Engineering
·
2026
·
IF 6.6
Youde Zhang,Kangping Cui,Zhimeng Li,Tao Jiang,Shuhan Yang
Construction of recoverable magnetic Fe₃O₄-NH₂/UiO-66/SiO₂–silica seed for CaF₂ crystallization. • Composite seed directs fluoride conversion from wastewater to CaF₂ solid. • UiO-66/SiO₂ interface promotes ion enrichment and heterogeneous nucleation. • Magnetic recovery reduces the loss of fine CaF₂-loaded seed particles. • Integration of fluoride removal, CaF₂ recovery and solid-liquid separation. Calcium-based precipitation is widely used for treating concentrated fluoride wastewater, but rapid homogeneous nucleation often generates fine CaF₂ particles that are difficult to recover. In this study, a silica-supported Fe₃O₄-NH₂/UiO-66 composite was developed as a magnetically recoverable crystallization seed for directing CaF₂ formation. At an initial fluoride concentration of 2000 mg/L, a Ca:F molar ratio of 0.8:1, 0.5 g seed dosage, pH 7–8, and 25 °C reduced residual fluoride to 2.56 mg/L, corresponding to 99.87% removal. Ca 2+ -free tests yielded equilibrium fluoride uptakes of 570 and 755 mg/g for UiO-66 and the composite, respectively, indicating that adsorption contributed to interfacial enrichment but was insufficient to account for the high fluoride conversion after Ca 2+ addition. Thermodynamic analysis showed that the initial saturation index increased from 3.1 to 7.5 and relative supersaturation from 28.9 to 288 as the initial fluoride concentration increased from 250 to 2000 mg/L. The crystallization rate followed a supersaturation-dependent power law with a kinetic exponent of 2.146 (R 2 = 0.993). After 8 cycles, fluoride-removal and magnetic-recovery efficiencies remained at 80.09% and 80.50%, respectively. In actual industrial wastewater, 98.82% fluoride removal was achieved after pH adjustment to 7. These results demonstrate the potential of Fe₃O₄-NH₂/UiO-66/SiO₂ as a reusable crystallization seed for fluoride recovery.
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DOI
高影响因子
危险品化学品经营许可证（带存储）