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JOURNAL OF POWER SOURCES · 2019 · IF 7.467

In situ template reaction method to prepare three-dimensional interconnected Fe-N doped hierarchical porous carbon for efficient oxygen reduction reaction catalysts and high performance supercapacitors

Pengfei Tian,Jianbing Zang,Shiwei Song,Shuyu Zhou,Hongwei Gao,Hanqing Xu,Xueqing Tian,Yanhui Wang

A novel in situ templates etching method is used to prepare three-dimensional (3D) interconnected Fe-N doped hierarchical porous carbon materials. Citric acid serves as a carbon source and etchant. Fe 2 O 3 nanoparticles not only provide the iron source by in situ etching but also act as templates to construct the hierarchical porous structure. The prepared optimal sample displays a high specific surface area of 1643.6 m 2  g −1 with an interconnected abundant hierarchical porous structure and homogeneous distribution of Fe and N elements in the carbon. The optimized sample displays excellent catalytic oxygen reduction reaction (ORR) performance with a positive half-wave potential (0.85 V), efficient four-electron reaction and excellent durability, which are superior to those of Pt/C (20 wt%) catalyst. Meanwhile, due to the unique interconnected hierarchical porous structure, it also exhibits a high specific capacitance of 378.6 F g −1 at 0.5 A g −1 and an excellent rate capability of 276.6 F g −1 at 20 A g −1 as supercapacitors electrode materials in 6 M KOH. This work provides a simple design for the preparation of 3 D interconnected Fe-N doped hierarchical porous carbon electrode materials that display potential applications in ORR catalysts and supercapacitors.

研究领域: 材料科学 · 能源化学
✓ 已验证 DOI 高影响因子
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WASTE MANAGEMENT · 2021 · IF 7.145

Optimization of heterogeneous Fenton-like process with Cu-Fe@CTS as catalyst for degradation of organic matter in leachate concentrate and degradation mechanism research

Chengrui Guo,Xia Qin,Rui Guo,Yue Lv,Mingran Li,Ziyuan Wang,Tinghui Li

The heterogeneous Fenton-like process with bimetallic chelated magnetic chitosan aerogel (Cu-Fe@CTS) as catalyst was applied to treat pre-coagulated leachate nanofiltration concentrate. The process conditions were optimized by Box-Behnken Design (BBD) and the maximum UV 254 removal reached 96.06% under the conditions of temperature 87.62 °C, oxidant dosage 0.2395 mol/L and catalyst dosage 1 g/L. The TOC concentration was reduced from 847.5 to 99.7 mg/L and COD concentration was reduced from 1625 to 464 mg/L. The three-dimensional (3D) fluorescence analysis showed that most of Fulvic acid-like (FA-like) was removed. The adsorption experiment showed that the catalyst reached the adsorption balanced after 60 min and the corresponding FA adsorption removal reached 14.1%. The addition of Tert-butanol (TBA) reduced the FA removal by 59.4%, indicating that the hydroxyl radicals ( OH) was the main active species. Experiments of the OH capture at different pH showed that the Fenton-like system produced more OH at pH of 4, at which the maximum FA removal was 96.61%, while the FA removal still reached 94.26% at pH of 7. The OH capture at different temperature showed that the Fenton-like system produced more OH at 90 °C. KI and TBA shielding experiments showed that OH was produced on the catalyst surface rather than being produced by catalysis of free metal ions in the solution.

研究领域: 环境科学 · 催化化学
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JOURNAL OF POWER SOURCES · 2020 · IF 8.247

Molecular-confinement synthesis of sub-nano Fe/N/C catalysts with high oxygen reduction reaction activity and excellent durability for rechargeable Zn-Air batteries

Danke Chen,Jiapeng Ji,Zhongqing Jiang,Min Ling,Zhongjie Jiang,Xinsheng Peng

Transition metal-nitrogen-carbon (M/N/C) catalysts, Fe/N/C in particular, with low cost, good tolerance to methanol and promising activity has great potential to replace Pt-based catalysts in oxygen reduction reaction (ORR). However, for metal atoms are easy to migrate and agglomerate during pyrolysis , it still remains a challenge to rationally design precursors to synthesize highly active M/N/C without significant agglomeration of metal sites. In this work, we propose a molecular-confinement strategy to synthesize sub-nano Fe/N/C catalysts by confinement [Fe(CN) 6 ] 3- in zeolitic imidazolate framework-8 (ZIF-8) crystals to minimize the agglomeration of Fe atoms during pyrolysis . The half-wave potential of the prepared sub-nano Fe/N/C is 40 mV superior to that of commercial 20% Pt/C in alkaline medium . Besides, it has electron transfer number close to 4.00, with below 0.5% H 2 O 2 yield, excellent long-term stability with only −5 mV shifts after 10000 cycles, and superb methanol tolerance. When utilized in Zn-air batteries as the cathode, it exhibits better activity, stability, and higher specific capacity than that of Pt–RuO 2 /C, showing a good potential for air cathode.

研究领域: 材料科学 · 电化学
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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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JOURNAL OF HAZARDOUS MATERIALS · 2024 · IF 12.2

pH dependence of reactive oxygen species generation and pollutant degradation in Fe(II)/O2/tripolyphosphate system

Chengwu Zhang,Anqi Yang,Bing Qin,Wei Zhao,Chuipeng Kong,Chuanyu Qin

It has been reported that tripolyphosphate (TPP) can effectively enhance the activation of O 2 by Fe(II) to remove organic pollutants in the environment. However, the influence of solution pH on the generation and conversion of reactive oxygen species (ROS) and their degradation of pollutants in the Fe(II)/O 2 /TPP system needs further investigation. In this study, we demonstrated that O 2 •– and •OH were the main ROS responsible for degradation in the system at different pH conditions, and their formation rates were calculated using a steady-state model. Experiments combined with density functional theory (DFT) calculations showed that the p -nitrophenol (PNP) degradation pathway in the Fe(II)/O 2 /TPP system is regulated by solution pH. Specifically, at pH = 3, the existence of Fe(II) in the solution is dominated by [Fe(II)(HTPP) 2 ] 2− , which leads to a rapid conversion from O 2 and HO 2 • to generate •OH, and PNP is primarily oxidatively degraded. However, at pH = 5/7, [Fe(II)(TPP) 2 ] 4− is taking the lead with which O 2 •– is accumulated in the solution due to the slow conversion to •OH in this condition, and the PNP is mainly reductively degraded. This study proposes a new strategy to achieve the targeted oxidative/reductive removal of different types of pollutants by simply varying the solution pH in the Fe(II)/O 2 /TPP system.

研究领域: 环境科学 · 化学 · 污染控制 · 活性氧物种
✓ 已验证 DOI PubMed 高影响因子
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Advanced Optical Materials · 2024 · IF 8

Designing Photochromic Materials La2MgSnO6:Er,Fe with Dynamic Luminescence Modulation for Dual-mode Optical Information Reading

Rongyi Kuang,Huiwang Lian,Yunfei Zhu,Simin Gu,Lin Huang,Bo-Mei Liu,Jing Wang

Inorganic photochromic luminescent materials hold immense promise as potential candidates for optical information storage applications. Unfortunately, static and single reading mode of photochromic luminescent materials in bright and dark environments pose a security threat to the stored information. Here, a novel material La 2 MgSnO 6 :Er 3+ ,Fe 3+ is developed, possessing both reversible photochromic and adjustable upconversion/downconversion photoluminescent (PL) properties. Upon exposure to 275 nm ultraviolet (UV) light, the sample changes in color from white to brown. And this transformation rapidly reverses when exposed to 365 nm UV light, resulting in a corresponding alteration in luminescence intensity. Notably, when combined with photochromic, the 980 nm excited upconversion PL maintains stable luminescence, while the 365 nm excited downconversion PL exhibits significant intensity changes. Inspired by this unique feature, a dark-field selective dual-mode reading is proposed that depends on the excitation wavelength, including static decrypt in long-time cases and dynamic reading in time-limited situations. These findings have the potential to revolutionize high-security data storage applications and drive advancements in the field.

研究领域: 材料科学 · 光电技术 · 信息技术 · 光子学
✓ 已验证 DOI 高影响因子
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Advanced Composites and Hybrid Materials · 2025 ·Vol. 8 ·期 6 ·394 · IF 21.8

A strategy for optimizing microstructure to simultaneously improve the strength and plasticity of W-Ni-Fe alloy

Wu Chongji,Yang Lu,Qian Zhu,Yan Zupeng,Sun Xia,Hu Weiqiang,Ma Zongqing

The conventional sintered W-Ni-Fe alloy encounters challenges in achieving both high strength and plasticity simultaneously, primarily due to its inadequate organizational compatibility. To address this issue, we developed a novel approach combining in situ freeze-drying and straightforward liquid-phase sintering techniques to effectively control the microstructure of 93W-4.9Ni-2.1Fe alloys. The corresponding W-Ni-Fe alloy in this work simultaneously takes into account ultrafine W grains (28.3 µm), low W-W connectivity (CW-W = 0.31), and suitable γ phase volume fraction (20.2%), which is currently difficult for traditional W-Ni-Fe alloys to achieve. The minute dimensions of nanopowder play a crucial role in inhibiting Ostwald ripening and facilitating W grain refinement. Additionally, the extensive surface area of nanopowder enhances capillary penetration, leading to effective homogenization of high γ phase volume. As a result, the freeze-dried W-Ni-Fe alloy simultaneously achieves high strength (1010 MPa) and high plasticity (31%), which provides a new insight for the further development of W-Ni-Fe alloy industries.

研究领域: 材料科学 · 冶金学 · 机械工程
✓ 已验证 产品关联 DOI 高影响因子
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ANALYST · 2013 ·Vol. 138 ·期 16 ·4526-4531 · IF 3.969

A nanosized metal–organic framework of Fe-MIL-88NH2 as a novel peroxidase mimic used for colorimetric detection of glucose

Ya Li Liu,Xi Juan Zhao,Xiao Xi Yang,Yuan Fang Li

In this paper, a nanosized porous metal–organic framework, Fe-MIL-88NH2, was facilely prepared with a uniform octahedral shape by the addition of acetic acid, and for the first time was demonstrated to possess intrinsic peroxidase-like activity. Kinetic analysis and electron spin resonance measurements indicated that the catalytic behavior was consistent with typical Michaelis–Menten kinetics and follows a ping-pong mechanism. As a novel peroxidase mimic material, Fe-MIL-88NH2 shows the advantages of high catalytic efficiency, ultrahigh stability and high biocompatibility in aqueous medium compared with natural enzymes and other peroxidase nanomimetics. Here, Fe-MIL-88NH2 was used to quickly catalyze oxidation of the peroxidase substrate 3,3′,5,5′-tetramethylbenzidine (TMB) in the presence of H2O2 to produce a colored product, which provided a simple, sensitive and selective method for the colorimetric detection of glucose. Glucose could be linearly detected in the range from 2.0 × 10−6 to 3.0 × 10−4 M with a detection limit of 4.8 × 10−7 M, and the color variation for glucose response was also obvious by visual observation at concentrations as low as 2.0 × 10−6 M. More importantly, the colorimetric method could be successfully applied to the determination of glucose in diluted serum samples.

研究领域: 生物分析化学 · 纳米生物技术 · 酶模拟 · 临床检验 · 分子诊断
✓ 已验证 DOI 高影响因子
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SEPARATION AND PURIFICATION TECHNOLOGY · 2018 · IF 3.927

A novel carbon-coated Fe-C/N composite as a highly active heterogeneous catalyst for the degradation of Acid Red 73 by persulfate

Cui Wang,Qiangqiang Yang,Zhenhong Li,Kun-Yi Andrew Lin,Shaoping Tong

A magnetic carbon-coated Fe-C/N composite was synthesized by a simple impregnation method and its performance in activating persulfate (PS) to degrade Acid Red 73 (AR 73) was investigated. The as-prepared carbon-coated Fe-C/N hybrid material was characterized via transmission electron microscopy , Raman spectra, X-ray diffraction and X-ray photoelectron spectrum. Degradation experiments showed that 98.11% of AR 73 could be degraded in 10 min, but its COD was partly removed. The effects of initial reaction pH and temperature were also evaluated. An increase of temperature was beneficial for the removal of AR 73, while the increase of pH had an opposite result. The activation energy of the AR 73 degradation was determined to be 46.12 KJ/mol, smaller than those in relative literatures. The recycling test showed that the carbon-coated Fe-C/N composite had good stability. The mechanism study indicated that the catalytic performance of Fe-C/N was due to the synergistic effect between Fe 3 C and Fe 3 N, and the N doped carbon shell suppressed the rate of Fe leaching, thus enhancing its stability.

研究领域: 环境科学 · 材料科学
✓ 已验证 DOI 高影响因子
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2015 · IF 7.435

A simple strategy for fabrication of Pd@MIL-100(Fe) nanocomposite as a visible-light-driven photocatalyst for the treatment of pharmaceuticals and personal care products (PPCPs)

Ruowen Liang,Shuiguang Luo,Fenfen Jing,Lijuan Shen,Na Qin,Ling Wu

The effective treatment of pharmaceutical and personal care products (PPCPs) contained wastewater remains a significant but challenging task for the environmental restoration. In this work, a novel Pd@MIL-100(Fe) nanocomposite has been successfully fabricated via a facile alcohol reduction approach. The resulting Pd@MIL-100(Fe) has exhibited superior photoactivity toward degradation of three typical PPCPs, that is theophylline, ibuprofen and bisphenol A, under visible light irradiation ( λ   ≥   420   nm). Its photoactivity is also much higher than that of original-MIL-100(Fe). Combining with photoelectrochemical analyses, it could be revealed that the introduction of Pd NPs would minimize the recombination of photogenerated electron–hole pairs, thereby improving the photocatalytic performance. Furthermore, the effects of different kinds of metals, the loading amount of noble-metal, the pH value of reaction solution and initial concentration of hydrogen peroxide on the photocatalytic degradation activities have been measured in detail. In addition, a possible photocatalytic reaction mechanism has been investigated. This work has not only represented the first example of using the MOFs photocatalysts to remove the aqueous PPCPs, but also offered useful information on the fabrication of efficient MOF photocatalysts for environmental restoration.

研究领域: 环境科学 · 材料科学
✓ 已验证 DOI 高影响因子
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CARBON · 2022 · IF 11.307

Uncovering the optimal pyrolysis temperature of NH2-MIL-88B-derived FeOX/Fe@porous carbon composites for the ultrasensitive electrochemical detection of baicalin in natural plant samples

Jiao Li,Yuefan Wang,Chenxi Wang,Yilin Wang,Yaqi Yang,Jia Chen,Chunyan Li,Yixi Xie,Pengcheng Zhao,Junjie Fei

Baicalin obtained from natural plants has essential medical value, so the development of accurate and sensitive quantitative methods for it is one of the most important tasks. Here, the FeO X /Fe@porous carbon composite (Fe@C) was synthesized by solvothermal method and carbonized at different temperatures under an N 2 atmosphere, and an electrochemical sensor designed based on this material was applied to the accurate and rapid determination of baicalin. According to the results of physical and electrochemical characterization, Fe@C at different pyrolysis temperatures exhibited different morphologies and different electrochemical properties , while the Fe@C pyrolyzed at 800 °C had the optimum performance. Compared with NH 2 -MIL-88B, the pyrolysis greatly reduces the charge transfer internal resistance of the material and has a larger porosity and specific surface area, resulting in an eminent electrochemical signal for the detection of baicalin. The sensor Fe@C-800/GCE not only has a linear range of 4 nM–700 nM with a low limit of detection of 1.16 nM for the detection of baicalin, but also has outstanding repeatability, anti-interference and stability for the detection of baicalin in several natural plant samples and herbal medicines samples. This work presents several pyrolytic NH 2 -MIL-88B as electrochemical sensors for the detection of baicalin for the first time, providing a novel idea for the application of MOFs derivatives in environmental analysis.

研究领域: 分析化学 · 生物医学工程 · 材料科学
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ENERGY & FUELS · 2020 · IF 3.421

Thiocyanate Ion Ligand-Induced Atomically Dispersed Fe–N–S Tridoped Hollow Catalyst for High-Performance Zinc–Air Rechargeable Batteries

Cheng Yang,Chengyong Shu,Zhuofan Gan,Chen Lai,Jijun Ma,Wei Tang,Yuping Wu

ZIF-8-derived Fe–N–S triple doping hollow-shell nanoparticles are prepared by the surface modification of SCN– ligands. Fe3+ ions are highly adsorbed on the SCN–-modified layer, forming a hollow-shell rhombic dodecahedron particle after pyrolysis. Doping extra S atom is found to be an effective method to increase the density of atomically dispersed active sites and boost their catalytic performance. The H-ZIF-Fe-SCN catalyst shows good bifunctional stability toward the oxygen reduction reaction and the oxygen evolution reaction in alkaline solution, the half-wave potential for the H-ZIF-Fe-SCN catalyst was recorded to be 0.889 V vs reverse hydrogen electrode, and a maximum power performance of 158.8 mW cm–2 was achieved when it was used as a cathode catalyst in zinc–air batteries.

研究领域: 材料科学 · 电化学 · 能源存储与转换
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