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JOURNAL OF ALLOYS AND COMPOUNDS · 2017 · IF 3.133

Fe, Co bimetal activated N-doped graphitic carbon layers as noble metal-free electrocatalysts for high-performance oxygen reduction reaction

Ce Han,Xiangjie Bo,Jian Liu,Mian Li,Ming Zhou,Liping Guo

In this work, a novel catalyst in form of Fe, Co bimetallic alloy activated N-doped graphitic carbon layers (NC/Fe 10-x Co x ) without metal core is rationally fabricated through a simple pyrolysis method and applied for efficient oxygen reduction reaction (ORR) catalysis. The NC/Fe 10-x Co x catalysts have exhibited superior electrocatalytic ORR performance comparable to commercial Pt/C via a four-electron pathway under the same loading in alkaline media with outstanding durability and complete methanol tolerance. The improvement of ORR performance can be attributed to the synergistic effect of Fe, Co bimetallic activation on nitrogen-doped graphitic carbon layers, rich pore structure and uniformly dispersed dopants in the carbon matrix.

研究领域: 材料科学 · 电化学
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Journal of Chemistry · 2023 · IF 3

Rapid and Efficient Degradation of Ceftiofur Sodium by 5,6-Dimethylbenzimidazole-Modified ZIF(Fe/Co)x@CNF Nanocomposites

Hao Fu,Aotian Gu,Peng Wang,Chunhui Gong,Zhiying Li,Kai Chen,Yi Yang

The exploration of transforming various metals as metal sources into metal organic frameworks (MOFs) has attracted considerable attention in recent years. This study used triethylamine and 5,6-dimethylbenzimidazole (DMBIM) to modify the iron-doped cobalt zeolite imidazole framework on carbon fiber structure. The results showed that the ZIF(Fe/Co)1.25@CNF exhibited high CEF removal efficiency that over 97% of ceftiofur sodium (CEF) was removed within 10 min, which was significantly higher than that of the common ZIF-67 materials. Compared with other ZIF-67 composites, ZIF(Fe/Co)x@CNF has a larger specific surface area, resulting in a larger contact area and more active sites during the reaction. After the introduction of DMBIM, the ZIF(Fe/Co)1.25@CNF not only easily separated from the solution but also enhanced the hydrophobicity, which provided higher catalytic stability and catalytic performance. In addition, the effects of different catalyst ratios, pollutant concentrations, solution pH, and different radicals (•OH, SO4•−, 1O2) on the activation of peroxymonosulfate (PMS) were investigated. The mechanism of degradation was elucidated by electron paramagnetic resonance experiments. This study provides a new perspective for the preparation of high-performance MOF catalysts with excellent catalytic performance and may facilitate the application of MOF materials in more practical situations.

研究领域: 环境科学 · 材料科学 · 药物化学
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SCRIPTA MATERIALIA · 2024 · IF 5.3

Fe-Co-Ni-Cu high entropy magnetic nanoparticles with high magnetothermal properties

Mengyun Jia,Dingliang Liang,Qing Du,Hui Wang,Yuan Wu,Suihe Jiang,Xiaobin Zhang,Haihui Ruan,Xiongjun Liu,Zhaoping Lu

Magnetothermal therapy (MT) is a noninvasive cancer treatment that has shown great promise in recent years. However, the low magnetothermal efficiency of the existing magnetic nanoparticles used in MT has been an obstacle to their widespread applications. In this work, we report a new class of Fe-Co-Ni-Cu high-entropy magnetic nanoparticles (HEMNPs) with exceptional magnetothermal properties synthesized by a thermal decomposition method. The fabricated HEMNPs, having an average diameter of 60–70 nm, exhibited a saturation magnetization of 42.4 emu/g and coercivity of 129.5 Oe. The hyperthermia measurement reveals that the HEMNPs have a maximum specific loss power of 202 W/g at the concentration of 2 mg/ml under an alternating magnetic field with an intensity of 46 Oe and a frequency of 266 kHz, demonstrating the great potential for MT applications. Our results demonstrate that the high-entropy concept can be extended to develop high-performance magnetic nanoparticles for MT applications.

研究领域: 材料科学 · 纳米技术 · 癌症研究 · 治疗工程
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Journal of Materials Chemistry A · 2022 ·Vol. 10 ·期 37 ·19757-19768 · IF 14.511

Electronic engineering of amorphous Fe–Co–S sites in hetero-nanoframes for oxygen evolution and flexible Al–air batteries

Min Lu,Li An,Jie Yin,Jing Jin,Rui Yang,Bolong Huang,Yang Hu,Yong-Qing Zhao,Pinxian Xi

The electrochemical oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are key electrochemical processes in metal–air batteries and water splitting devices. Aluminium–air batteries, as an important type of metal–air battery, have been considered to be promising power candidates for flexible electronics. Here, we describe electronically engineered amorphous Fe–Co–S sites embedded in Prussian blue analogue (FeCoSx-PBA) hetero-nanoframes. The experimental results and DFT calculations reveal the critical role of the introduced FeCoSx layer to PBA, which enhances the electron transfer and alleviates the overbinding effect of OH* during the OER. The FeCoSx-PBA hybrid system supplies an optimized electronic structure for the alkaline OER, which is also confirmed by the much-lowered overpotential (266 mV at 10 mA cm−2) for the alkaline OER. Furthermore, a flexible Al–air battery based on an FeCoSx-PBA cathode catalyst exhibits a high peak power density (58.3 mW cm−2) and energy density (1483 W h kgAl−1), and outstanding stability for more than 50 h of operation under bending or stretching conditions, demonstrating its potential in the practical application of flexible electronic devices. Our results may provide a new strategy of modulating the electronic structure of air electrode catalysts to efficiently promote the reactivity of alkaline OER and Al–air battery processes.

研究领域: 材料科学 · 电化学 · 能源技术
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SENSORS AND ACTUATORS B-CHEMICAL · 2019 · IF 6.393

Fe-Co-Co prussian blue analogues as a novel co-reaction accelerator for ultrasensitive electrochemiluminescent biosensor construction

Qian Wu,Peijin Wang,Xue Yang,Min Wei,Mao Zhou,Yuxin Pu,Mingxiao Zhang

An ultrasensitive electrochemiluminescence (ECL) biosensor was constructed by using Fe y Co 3-y [Co(CN) 6 ] 2 prussian blue analogues (Fe-Co-Co PBAs) as a novel electrochemically regenerable co-reaction accelerator for methotrexate (MTX) detection. In this work, we synthesized the core-shell Fe-Co-Co [email protected] 3 N 4 tags with luminophores and co-reaction accelerators via a facile and green method. To the best of our knowledge, it is the first time that Fe-Co-Co PBAs was used as an efficient co-reaction accelerator of the carboxylated graphene-like carbon nitride /peroxydisulfate (C-g-C 3 N 4 /S 2 O 8 2− ) ECL system for signal amplification. In view of the prominent quenching effect of MTX on the ECL response of the C-g-C 3 N 4 , the proposed ECL biosensor exhibited high sensitivity to quantify the concentration of MTX from 5 pM to 10 μM with a detection limit of 1.1 pM. Simultaneously, the biosensor has also been successfully applied to MTX detection in human serum and urine samples with reasonable recoveries. Hence, the proposed method holds a new perspective of PBAs nanomaterials in biosensing and provides a potential analysis method for the rapid detection of MTX in biological systems.

研究领域: 分析化学 · 纳米技术 · 生物医学工程 · 临床化学
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ELECTROCHIMICA ACTA · 2017 · IF 4.798

Sandwich-type Bimetal-Organic Frameworks/Graphene Oxide Derived Porous Nanosheets doped Fe/Co-N Active Sites for Oxygen Reduction Reaction

Qijian Niu,Junxia Guo,Yunhui Tang,Xindong Guo,Jun Nie,Guiping Ma

In this work, a bimetal-organic framework/graphene oxide with sandwich-type structure as a precursor is prepared by the solvent-thermal approach. A nanoporous reduced graphene oxide (rGO) nanosheets enriched with Fe, Co and N (Fe/Co-N) co-doped active sites is prepared followed by a high temperature carbonization and acid leaching (AL) process. When the molar ratio of Fe/Co is 0.40 before carbonization , the prepared sample exhibits optimized electrocatalytic activity (a high onset potential (0.98   V vs. RHE), half-wave potential (0.84   V vs. RHE), and a large limiting current density (-5.46   mA   cm −2 at 0.21   V vs. RHE) as oxygen reduction reaction (ORR) electrocatalysts . Most importantly, the duration stability and methanol tolerance of the as-prepared sample are better than common commercial 20   wt% Pt/C under 0.10   M KOH alkaline condition. These results demonstrate the co-doping of bimetal Fe/Co and heteroatom N, excellent electrical conductivity of rGO and large surface area of nanoporous structure enhance the electrocatalytic activity . The successful synthesis of such nanoporous rGO nanosheets provides a facile way to explore a series of 2D non-precious metal electrocatalysts for energy conversion and storage devices.

研究领域: 材料科学 · 电化学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Fe-Co/Fe3C dual active sites catalysts supported on nitrogen-doped graphitic carbon for ultrafast degradation of high concentration Rhodamine B

Yuying Chen,Caiwen Wu,Haiyang Xie,Zhaoyan Deng,Yiming Liu,Yanjuan Zhang,Zuqiang Huang,Huayu Hu,Tao Gan

Iron-based catalysts have garnered great attention as alternatives for Fenton-like catalysts in the degradation of organic compounds. However, there is a demand for the synthesis of highly efficient iron-based catalysts that can solve the problems of iron dissolution and poor stability. Herein, nitrogen-doped graphitic carbon-supported Fe-Co/Fe 3 C dual active sites catalyst (Fe-Co/Fe 3 C-NC) is successfully prepared by ball milling method combined with subsequent high-temperature self-reduction. 0.5 wt%-Fe-Co/Fe 3 C-NC shows high efficiency in the activation of peroxymonosulfate (PMS) for the ultrafast degradation of high concentration Rhodamine B (200 mg/L of RhB is completely degraded within 8 min and the degradation rate constant is as high as 0.5066 min −1 ), as well as high stability and good reproducibility, attributing to the synergistic mechanism between the dual active sites (Fe-Co and Fe 3 C) and the adsorption sites (Fe 3 C and pyrrolic-N). Chemical quenching experiments and electron paramagnetic resonance indicate that the prepared 0.5 wt%-Fe-Co/Fe 3 C-NC exhibits outstanding activation for PMS by generating reactive oxygen species (SO 4 •− , • OH, 1 O 2 ) and high-valent FeCo=O species. This work shows useful insights into the synthesis of iron-based dual active sites catalysts, providing exciting chances for the highly efficient degradation of high concentration organic wastewater.

研究领域: 环境科学 · 催化化学
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Journal of Water Process Engineering · 2024 · IF 6.3

Improvement of heterogeneous electro-Fenton oxidation of dimethyl phthalate by embedding Fe/Co bimetallic active sites into waste wine lees biochar

Shenbao Qu,Wenpei Guo,HongDi Mou,Ruyi Wang,Man Wei,Xia Hu

Phthalates (PAEs) are frequently detected in the water environment and pose a severe threat to the ecosystem and human health. Electro-Fenton technology is regarded as an effective approach to degrade PAEs; however, the preparation of inexpensive and efficient cathode materials has restricted its further application. In this study, Fe/Co bimetallic sites were incorporated into solid waste wine lees to synthesize highly active heterogeneous catalyst, and dimethyl phthalate (DMP) was chosen as the target pollutant to investigate the activity of the catalyst. Both the degradation of DMP and the removal of total organic carbon (TOC), the performance of Fe/Co co-modified biochar (FeCo@NOPC) is superior to that of Fe (Co) alone (Fe@NOPC/Co@NOPC) and modified biochar (NOPC). Under neutral conditions. Within 5 h, the DMP removal rate reached 89 % and TOC was reduced by approximately 40 %. The mechanism study reveals that the degradation of DMP is mainly attributed to the OH generated by the cathode, and the anodic oxidation and cathode adsorption only play minor roles. Finally, the degradation path of DMP was analyzed by LC-MS technique. This study offers a novel way to utilize solid waste and reduce the cost of heterogeneous electro-Fenton system.

CAS / MDL: 10026-22-9 131-11-3
研究领域: 环境科学 · 材料科学
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Small · 2023 ·Vol. 19 ·期 23 ·2300106 · IF 13.3

The Inducement and “Rejuvenation” of Li Dendrites by Space Confinement and Positive Fe/Co-Sites

Ziqin Liu,Xin Dong,Jing Wen,Pu Hu,Chaoqun Shang

The high reactivity of Li metal and the inhomogeneous Li deposition leads to the formation of Li dendrites and “dead” Li, which impedes the performance of Li metal batteries (LMBs) with high energy density. The regulating and guiding the Li dendrite nucleation is a desirable tactic to realize concentrated distribution of Li dendrites instead of completely inhibiting dendrite formation. Here, a Fe-Co-based Prussian blue analog with hollow and open framework (H-PBA) is employed to modify the commercial polypropylene separator (PP@H-PBA). This functional PP@H-PBA can guide the lithium dendrite growth to form uniform lithium deposition and activate the inactive Li. In details, the H-PBA with macroporous structure and open framework can induce the growth of lithium dendrites via space confinement, while the positive Fe/Co-sites lowered by polar cyanide (−CN) of PBA can reactivate the inactive Li. Thus, the Li|PP@H-PBA|Li symmetric cells exhibit long-term stability at 1 mA cm −2 for 1 mAh cm −2 over 500 h. And the Li-S batteries with PP@H-PBA deliver favorable cycling performance at 500 mA g −1 for 200 cycles.

研究领域: 材料科学 · 电化学 · 能源存储
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NEW JOURNAL OF CHEMISTRY · 2023 ·Vol. 48 ·期 4 ·1757-1770 · IF 3.3

A self-synthesised non-homogeneous MoS2/Fe–Co–N–BC composite catalyst as an activator for peroxomonosulfate activation for efficient degradation of perfluorooctanoic acid

Ling Tao,Jiepu Zhang,Fangke Yu

In this study, in order to achieve efficient activation of persulfate, we added MoS2 as a co-catalyst to the iron, cobalt and nitrogen modified biochar (Fe–Co–N–BC) catalytic system. Analytical methods such as scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) demonstrated that the MoS2/Co–Fe–N–BC catalytic materials were successfully prepared. In the MoS2/Fe–Co–N–BC/PMS system, 97.5% of PFOA was removed within 180 min with Kobs of 0.074 min−1. Composites with different mass ratios of MoS2 and Co–Fe–N–BC/PMS in the non-homogeneous PMS system both exhibit excellent catalytic efficiency for TOC removal. In particular, MoS2/Fe–Co–N–BC obtained extraordinary catalytic efficiency through synergistic radical (SO4˙−, ˙OH) and non-radical (1O2, FeIV and FeV) processes, which was proved by the quenching experiments and the EPR testing. The analysis of the activation mechanism reveals that the three redox ion pairs Fe2+/Fe3+, Co2+/Co3+ and Mo4+/Mo6+ simultaneously participated in the activation of PMS, realizing multi-path electron transfer. And MoS2 played an excellent co-catalysis role in promoting the cycling of the valence states of the ions. Compared to Fe3+ and Co3+, the low valence states of Fe2+ and Co2+ can activate PMS more rapidly and produce more ˙OH and SO4˙−. However, the recycling efficiency of Fe2+ and Co3+ in the Fe–Co–N–BC system is low, and the presence of MoS2 improves the efficiency of Fe3+ and Co3+ reduction to Fe2+ and Co2+, respectively. The possible degradation pathways of PFOA were proposed. This study provides some references for the design of polymetallic-doped catalysts to degrade difficult-to-degrade organic pollutants.

研究领域: 环境科学 · 催化材料科学
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2025 · IF 3.8

Effect of rare earth oxides on the thermal stability of Mn-Fe-Co-Zn-O ceramics under high-temperature N2 atmosphere

Shuangjiang He,Junchang Wang,Chong Wang,Xiao Zhang,Sen Liang

The Mn-Fe-Co-Zn-O series is a widely used thermistor material, but its thermal stability is compromised by nitrogen glass encapsulation, limiting its application in electrical devices. To address this issue, La 2 O 3 and Y 2 O 3 were used as rare earth oxide dopants, and xR 2 O 3 -Mn 0.76 Fe 0.87 Co 1.07 Zn 0.3 O 4 (x = 0.0025, 0.005, 0.01, 0.02) negative temperature coefficient (NTC) materials were synthesized via solid-state sintering. The effect of rare earth doping on the electrical properties after high-temperature nitrogen annealing was investigated. After annealing at 750°C for 4 h, the variation in resistivity ( ρ 25 ) and material constant ( B 25/50 ) significantly decreases with increasing La doping. For the La-doped sample (x = 0.01), Δρ 25 decreased to 7.77% and ΔB 25/50 to 0.77% (for the Y-doped sample (x = 0.01), Δρ 25 decreased to 22.76% and ΔB 25/50 to 1.91%), compared to the undoped sample, where Δρ 25 reduced by 168.84% and ΔB 25/5 0 by 5.57%. This improvement was attributed to rare earth accumulation at grain boundaries, filling voids and forming R-O bonds, which inhibited oxygen vacancy migration and significantly reduced grain boundary resistance. Rare earth doping effectively improved the thermal stability and electrical consistency of NTC thermistor ceramics in high-temperature nitrogen atmospheres, offering a new strategy for high-temperature encapsulation applications. (Y-doped samples showed similar results, as detailed in the Supplementary Materials.)

CAS / MDL: 1312-81-8
研究领域: 材料科学 · 无机非金属材料 · 电子陶瓷 · 热敏材料 · 固态化学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Oxygen evolution and oxygen reduction catalyzed by Fe-Co-Ni ternary metal sulfides for rechargeable zinc-air battery

Zhaomin Lu,Guang Li,Kuang Sheng,Ting Wu,Wenwen Luo,Hu Zhou,Qingfeng Yi

Further enhancing the electrocatalytic performance of transition metal sulfides for oxygen evolution and oxygen reduction reactions (OER and ORR) is crucial for the development of high-efficiency electrochemical energy devices. Here, the highly efficient iron-doped nickel sulfide/cobalt sulfide heterostructure catalyst (Fe-NiS 2 /CoS 2 ) was successfully prepared via a combination of hydrothermal-sulfidation-reduction strategy. Physical characterizations coupled with electrochemical tests reveal that Fe doping plays a key role in the excellent performance of Fe-NiS 2 /CoS 2 by lowering charge transfer resistance, optimizing electronic structure, and promoting reaction kinetics synergistically. As a result, the Fe-NiS 2 /CoS 2 catalyst exhibits a bifunctional electrocatalytic reactivity with a low ΔE of 0.61 V, surpassing noble-metal-based catalyst and most of the reported iron-related sulfide bifunctional catalysts. Specifically, the catalyst exhibits low overpotentials of 265 mV at 10 mA cm −2 and 381 mV at 100 mA cm −2 for the OER, while maintaining an ORR E 1/2 of 0.88 V. Aqueous zinc-air battery (ZAB) based on Fe-NiS 2 /CoS 2 achieve the specific capacities of 678.5 mAh g Zn −1 and along with 200 h cycling stability. This work provides an effective approach to improving transition metal sulfides, with potential for broader application in OER/ORR-related energy technologies.

研究领域: 电化学 · 能量存储与转换 · 材料科学 · 纳米技术 · 催化
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