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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2022 ·Vol. 169 ·期 9 ·097508 · IF 4.386

Sensitive, Selective and Simultaneous Monitor of Multiple Heavy Metals in Environment Using a Low-Cost MIL-53(Fe)/Ag2CrO4 Modified GCE Sensor

Xiaomin Guo,Pinghua Chen,Hualin Jiang,Xiaoqiu Tang,Yiping Huang,Guanghui Wu,Jian Zhang

Due to the strong toxicity of heavy metal ions to public health and the environment, it is a great challenge to develop a method for ultra sensitive capture and determination of heavy metal ions effectively. Herein, a novel heterostructure composite (MIL-53(Fe)/Ag2CrO4, named MA(1:x)) was prepared by a simple method successfully. MA(1:x) modified GCE was applied to detect heavy metals ions simultaneously. Significantly, the designed MA(1:1)/GCE sensors performed outstanding detection performances. The wide ranges of 7.49 ∼ 320.00 μmol l−1 and 7.49 ∼ 320.04 μmol l−1 are obtained for Pb(II) and Cu(II) ions, respectively. The LOD of the MA(1:1)/GCE sensor was determined to be 27.40 nmol l−1 (5.68 ppb) for Pb(II) and 86.96 nmol l−1 (5.52 ppb) for Cu(II) ion simultaneously, which are lower than the allowable level of drinking water stipulated by the World Health Organization (WHO). Possible detection mechanism by the MA(1:1)/GCE was discussed. The MA(1:1)/GCE was successfully applied to monitor heavy metal ions locate in tap and river water. The recoveries are in the range of 93.86%–104.4%, which further proves the potential in analyzing real samples. Moreover, the MA(1:1)/GCE also showed excellent stability, selectivity, reproducibility. A novel method was provided to construct sensitive sensors for simultaneous analysis of different metal ions.

研究领域: 环境科学 · 分析化学
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Acta Biomaterialia · 2022 · IF 10.633

Fe(III)-coordinated N-[tris(hydroxymethyl)methyl]acrylamide-modified acrylic pressure-sensitive adhesives with enhanced adhesion and cohesion for efficient transdermal application

Longyi Nan,Jie Liu,Chao Liu,Peng Quan,Jianpeng Guo,Liang Fang

Pressure-sensitive adhesives are critical to the product's safety, efficacy, and quality in transdermal drug delivery systems. However, many defects of transdermal patches ( e.g. , insufficient adhesion, patch displacement, and “dark ring” phenomenon) remain. Herein, the N -[tris(hydroxymethyl)methyl]acrylamide (NAT)-modified acrylic pressure-sensitive adhesive coordinated with Fe(III) (AA-NAT/Fe 3+ ) was creatively proposed. Results demonstrated that the adhesiveness and cohesiveness of the optimized AA-NAT/Fe 3+ were higher by 1.8- and 9.7-fold, respectively, than those of commercially available DURO-TAK® 87-4098 due to the hydrogen bonding interaction of NAT-skin interface and coordination of NAT-Fe 3+ . Moreover, compared with that of DURO-TAK® 87-4098, the adhesion time of AA-NAT/Fe 3+ on the human forearm was remarkably prolonged, and no “dark ring” phenomenon was observed for AA-NAT/Fe 3+ after removal. After clonidine (CLO) was loaded into AA-NAT/Fe 3+ , controlled drug release and a drug transdermal behavior were endowed for CLO@AA-NAT/Fe 3+ in vitro and in vivo . AA-NAT/Fe 3+ still maintained superiority in adhesion and cohesion properties after CLO loading. These observations would contribute to the development of pressure-sensitive adhesives with outstanding adhesion and cohesion for transdermal patches. Statement of significance This N -[tris(hydroxymethyl)methyl]acrylamide-modified acrylic pressure-sensitive adhesive coordinated with Fe(III) has enhanced adhesion and cohesion properties, which provide a simple but effective strategy to solve the problems ( e.g. , insufficient adhesion, patch displacement, and “dark ring” phenomenon) in existing transdermal patches.

研究领域: 材料科学 · 药剂学 · 生物医学工程
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

BiO2-x@Fe nanospheres for enhanced degradation and antibacterial performances using synergistic photocatalysis and Fenton effect

Sihan Ma,Xinglin Yu,Zheng Han,Deng Long,Wentao Li,Jianglong Kong,Xue Bai

Bi 2 O 3 -based photocatalytic materials exhibit significant potential for pollutant and bacterial removal. However, their practical application in efficient water treatment is hindered by two key challenges, including an insufficient suppression of photogenerated carrier recombination and a narrow bandgap that restricts light absorption to low-density wavelengths. Additionally, while the Fenton reaction enhances catalytic activity, its effectiveness is compromised by iron sludge formation resulting from the rapid release of iron ions. In this work, BiO 2-x @Fe nanospheres were successfully synthesized via a facile hydrothermal method, integrating synergistic photocatalytic and Fenton-like activities. These nanospheres demonstrate exceptional performance in simultaneous bacterial inactivation and organic pollutant degradation under light irradiation . The strategic introduction of defect-rich active sites and surface hybrid architectures effectively suppresses photogenerated carrier recombination while retarding iron ion release kinetics, thereby enabling superior catalytic performance. This dual-functional system, integrating enhanced photocatalytic oxidation and Fenton-driven antibacterial mechanisms, achieves near-complete bacterial inactivation and efficient organic pollutant degradation under visible light irradiation. The synergistic interaction between photocatalysis and Fenton chemistry demonstrates exceptional potential for rapid, high-efficiency water purification applications.

研究领域: 环境科学 · 材料科学 · 纳米技术 · 化学工程 · 光催化
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IEEE TRANSACTIONS ON MAGNETICS · 2019 ·Vol. 55 ·期 12 ·1-7 · IF 1.651

Microstructure and Magnetic Properties of Fe/ZrSiO4 Composites Prepared by Mechanical Milling and Spark Plasma Sintering

Wentao Hu,Xi’an Fan,Zigui Luo,Fan Luo,Guangqiang Li,Yawei Li,Jian Wang

Fe/ZrSiO4 composite compacts with high thermal stability and excellent soft magnetic performance were prepared successfully by mechanical milling and spark plasma sintering. The effect of ZrSiO4 content on microstructure and magnetic properties of the Fe/ZrSiO4 composite compacts was investigated in detail. ZrSiO4 could be coated uniformly on the surface of Fe particles. With the increasing ZrSiO4 content, the core losses are effectively reduced, but the effective permeability and the saturation magnetic magnetization gradually decrease, while the coercivity has shown the opposite trend accordingly. The composite compact with 7.5 wt% ZrSiO4 has shown the superior structure and soft magnetic properties such as high saturation magnetic magnetization (202.20 emu/g), stable effective magnetic permeability (29.39), and lower core loss (4.53 W . kg-1 at 5 kHz). The results indicated that the Fe/ZrSiO4 composite compacts had potential application prospects in electromagnetic conversion equipment at medium and high frequencies.

研究领域: 材料科学 · 磁性材料 · 粉末冶金 · 复合材料 · 功能材料
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JOURNAL OF ALLOYS AND COMPOUNDS · 2016 · IF 3.014

Na2Co3[Fe(CN)6]2: A promising cathode material for lithium-ion and sodium-ion batteries

Yan Yuan,Junxiang Wang,Zongqian Hu,Haiping Lei,Donghua Tian,Shuqiang Jiao

A Prussian blue analogue, Na 2 Co 3 [Fe(CN) 6 ] 2 , has been fabricated by a facile co-precipitation method at room temperature as a potential cathode material for both lithium-ion and sodium-ion batteries. It found that the Na 2 Co 3 [Fe(CN) 6 ] 2 nanoparticles with a primary particle size of 30–40 nm have been synthesized, and exhibited an excellent electrochemical performance , including a long cycling behavior in lithium-ion batteries and a good rate performance in sodium-ion batteries. In lithium-ion batteries, the Na 2 Co 3 [Fe(CN) 6 ] 2 nanoparticles cathode can deliver an excellent cyclic performance with 73.0% retention of initial capacity after 50 cycles at 50 mA g −1 . Moreover, when Na 2 Co 3 [Fe(CN) 6 ] 2 is used as cathode material of sodium-ion batteries, it exhibits an outstanding rate performance exceeding 75.2% retention of initial capacity after 50 cycles at 200 mA g −1 . Therefore, the Na 2 Co 3 [Fe(CN) 6 ] 2 nanoparticles can be a potential cathode candidate for the application of lithium-ion and sodium-ion batteries due to its excellent electrochemical performance, easy preparation, low cost and environment benefits.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 纳米材料
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ANALYST · 2019 ·Vol. 144 ·期 8 ·2716-2724 · IF 4.019

A functional FePt@MOFs (MIL-101(Fe)) nano-platform for high efficient colorimetric determination of H2O2

Zunfu Hu,Yongheng Yin,Qingyun Liu,Xiuwen Zheng

The rapid and sensitive detection of H2O2 is of great importance for a series of industries. In this work, surface-modified FePt nanoparticles were loaded into metal–organic frameworks (MOFs, MIL-101(Fe)) in a facile in situ way and the resulting material (FePt@MOFs NCs) acted as a high efficient colorimetric detection agent. The as-prepared FePt@MOFs NCs possess a well-defined octahedron shape and high stability in water. Via the oxidation reaction of the chromogenic substrate 4,4′-bi-2,6-xylidine, the obtained FePt@MOFs NCs were proved to possess prominent peroxidase-mimic activity. Under the most favorable conditions, the linear range for H2O2 detection was 40 μM to 800 μM and the detection limit was 18.9 μM. Furthermore, FePt@MOFs NCs were successfully applied to the detection of H2O2 in real samples such as fruit juice. The developed colorimetric sensing platform is expected to have potential for the exact detection of H2O2 for the food, mining and bio-pharmaceutical industries, due to its high stability, sensitivity, rapidness and easy preparation.

研究领域: 分析化学 · 纳米生物技术 · 食品分析 · 环境监测 · 生物传感 · 材料科学 · 分子诊断
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Journal of Cleaner Production · 2020 · IF 7.246

Functional adjustment and cyclic application of Fe–Mn bimetal composite for Sb(V) removal: Transformation of iron oxides forms and a stable regeneration method

Kunlun Yang,Cheng Li,Xiaomin Wang,Yuanli Liu,Yizhou Li,Chuchen Zhou,Zheni Wang,Jiasheng Zhou,Zhen Cao,Xinhua Xu

In this work, the surface properties, functional groups and stability of Fe–Mn bimetal composite (FMBC) was modified through sintering to improve the weaknesses of pristine FMBC, such as poor separation performance, high amount of dissolved Fe and Mn, and easy phase transformation. Characterization analysis indicated that 2-line ferrihydrite in sintered FMBC (SFMC) gradually transformed into hematite with the phase-transition temperature of 450 °C. With the increasing sintering temperature and time, the dehydroxylation reaction enhanced and gradually became irreversible, while the BET surface area and porosity of SFMC firstly increased and then decreased, resulting in the initial increase and then sharp decrease of the amount of exposed hydroxyl groups on SFMC. The sintering treatment greatly improved the separation performance and stability of SFMC. 350 °C and 2 h were determined as the optimal sintering conditions of SFMC in this study and the calculated maximum adsorption capacity of optimal SFMC reached up to 95 mg/g. Freundlich model and pseudo-second-order kinetics model can describe the Sb(V) adsorption data well. As compared to pristine FMBC, optimal SFMC presented larger BET surface area and porosity, better separation performance and stability, lower dissolved Fe and Mn amount, larger cyclic adsorption efficiency and enough ability for Sb(V) removal in real textile wastewater. Furthermore, the inner sphere complexation between Sb(OH) 6 - and exposed hydroxyl groups played a key role in adsorption. Additionally, the NaCl + NaOH elution exhibited greater Sb(V) desorption performance and effectively retarded the phase transformation of SFMC than NaOH solution.

研究领域: 环境科学 · 材料科学
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ELECTROANALYSIS · 2023 ·Vol. 36 ·期 2 ·e202300237 · IF 3

Electrochemical detection of tryptophan in fish and pharmaceutical supplement at glassy carbon electrode modified with Fe doped ZnO nanoparticle

Toleshi Teshome,Shimeles Addisu Kitte,Abera Gure,Guta Gonfa

The co-precipitation approach was employed in this study to create Fe doped ZnO (Fe-ZnO) nanoparticles (NPs). To characterize the synthesized NPs, Ultra violet-Visible (UV-Vis) spectroscopy, X-ray diffraction (XRD), fourier transform infrared (FT-IR), scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) were used. Here, a novel electrochemical approach for the detection of tryptophan (Trp) using a glassy carbon electrode modified with Fe-ZnO NPs (Fe-ZnO/GCE) is demonstrated. The research findings revealed that Fe-ZnO/GCE enhanced the electron transfer rate of Trp oxidation. The sensitivity of Trp detection using Fe-ZnO/GCE in phosphate buffer solution (PBS) at pH 64.0 was significantly improved compared to bare GCE due to the electrocatalytic activity of Fe-ZnO NPs. Fe-ZnO/GCE exhibited a linear response with Trp concentrations ranging from 0.1 to 150 μM with the limit of detection (LOD) is 0.089 μM (3σ /m ) and limit of quantification (LOQ) about 0.3 μM (10σ /m ) using linear sweep voltammetry (LSV). The Fe-ZnO/GCE sensor was also effectively used to detect Trp in African catfish and multivitamin tablets. Trp analysis in real samples exhibited good recovery values of 89.60 to 99.15 %, demonstrating the accuracy and practicality of the method.

研究领域: 分析化学 · 生物医学工程 · 材料科学
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ACS Applied Nano Materials · 2025 · IF 5.5

Pt–Fe Bimetallic Nanoparticles Confined in Nitrogen-Doped Carbon Nanoshells as a Catalyst for the Reverse Water–Gas Shift Reaction

Xudong Zhao,Shuibo Wang,Hua Li,Yushi Wei,Yiming Li,Haocheng Li,Hongbo Yu,Kaijie Li,Haotian Li,Hongfeng Yin

Preventing nanoparticle migration and agglomeration on the surface of supported heterogeneous catalysts, especially at tailored bimetallic sites, poses a significant challenge. The reverse water–gas shift (RWGS) reaction is considered a promising route for converting CO2 into CO, an essential feedstock for industrial chemical production. Herein, a core–shell nanostructure anchoring on the surface was developed, which consists of a PtFe bicomponent core (∼2.6 nm) and a nitrogen-doped carbon nanoshell (∼1.3 nm). This structural design enhances the CO2 adsorption saturation, weakens the CO adsorption strength, and promotes hydrogen spillover. This PtFe core–shell material (Pt/Fe = 1:1) demonstrates an elevated reaction rate of 12.58 molCO2 gPt–1 h–1, with nearly 100% CO selectivity at 450 °C and atmosphere pressure. The activity is 5.1-fold higher than that of the Pt nanoparticle, attributed to the tuned geometric and electronic properties. The nitrogen-doped carbon nanoshell preserves the core–shell morphology at a high temperature. Moreover, the in situ experiments reveal the H-assisted dissociation/activation of the CO2 pathway for RWGS. The integration of the bimetallic synergy and core–shell structure is a potent strategy for thermal catalytic processes.

研究领域: 材料科学 · 催化化学 · 环境科学
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ACS Applied Materials & Interfaces · 2023 · IF 9.5

In Situ Construction of the Fe–Cu Hydroxide Interlocking Structure with Solution-Derived Cu/Ag Current Collectors for Flexible Symmetric Supercapacitors

Qia Zhang,JianXiong Zou,Jin Ai,XiaoTian Pan,DongHong Qiao,Seong Chan Jun,Vijaykumar V. Jadhav,Ling Kang,Chun Huang,Jian Zhang

The current collector serves as a crucial element in supercapacitors, acting as a medium between the electrode material and the substrate. Due to its excellent conductivity, a metal collector is typically favored. Enhancing the binding strength between the collector and the substrate as well as between the collector and the electrode material has emerged as a critical factor for enhancing the capacitance performance. In this study, a Ag film with a grass root-like structure was initially grown on a PI substrate through the surface modification and ion exchange (SMIE) process. This Ag interlocking structure contributes to strong binding between the PI substrate and Ag without compromising the mechanical properties of the Ag film. To further enhance the electrochemical properties at low scan rates, electroless-plated Cu was subsequently deposited on the Ag film to form the Cu/Ag current collector. Moreover, the Cu within the Cu/Ag current collector served as a precursor for the growth of FeOOH–Cu(OH)2 via a two-step in situ method. The resulting FeOOH–Cu(OH)2/Cu/Ag structure as a whole is binder-free. Supercapacitors employing symmetric FeOOH–Cu(OH)2/Cu/Ag structures were assembled, and their energy storage properties were investigated. The solution-based low-temperature process used in this study offers the potential for cost-effective and large-scale applications.

研究领域: 材料科学 · 能源存储
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Journal of Energy Storage · 2025 · IF 9.8

Electrosprayed hierarchical mesoporous Na₄Fe₃(PO₄)₂(P₂O₇)@C microspheres exhibit outstanding sodium-storage performance

Sikai Zhang,Rui Yin,Zhilong Tan,Minghai Zhao,Peng Zhou,Pei He,Runjing Zhang,Ziyan Wang,ZhiFeng Huang,Hai Hu,Li Liu

The mixed phosphate Na₄Fe₃(PO₄)₂(P₂O₇) (NFPP) via synergistic coordination of mixed [PO₄]/[P₂O₇] anion groups achieves a flat voltage plateau at 3.2 V (vs. Na + /Na) and a theoretical specific capacity of 129 mAh g −1 , but its practical application is still limited by its inherent low electronic conductivity. Through structural integration of polyanion-type cathode materials, this study innovatively designed and constructed hierarchical Na₄Fe₃(PO₄)₂(P₂O₇)@C mesoporous microspheres (NFPP@CMMS). The NFPP nanocrystals uniformly embedded in a three-dimensional interconnected meso porous carbon matrix (pore size distribution: 2–5 nm). Such hierarchical meso/micro-nano architectures provided expansive ion-exchange interfaces, accelerating Na + de/intercalation kinetics while enhancing electronic conductivity and mitigating structural collapse during cycling. Consequently, the NFPP@CMMS delivers exceptional reversible discharge capacity (121 mAh g −1 at 0.1C), outstanding rate capability (72 mAh g −1 at 50C), and superior cycling stability (90.70 % capacity retention after 3500 cycles at 5C). This triple-synergy strategy—combining nano-confinement effects, interconnected mesoporous channels, and carbon-encapsulated network—provides a novel pathway for developing practical sodium-ion battery cathodes.

CAS / MDL: 57-55-6 7782-63-0
研究领域: 材料科学 · 电化学 · 储能技术 · 纳米材料
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CHEMICAL PAPERS · 2024 ·Vol. 78 ·期 6 ·3761-3772 · IF 2.1

Fabrication of the MIL-101(Fe)@Ag composite SERS substrate for the detection of formaldehyde

Chen Yufeng,Zhao Ning

Surface-enhanced Raman scattering (SERS) has been widely applied in various fields due to its high sensitivity and rapid response capability. In this paper, a MIL-101(Fe)@Ag composite SERS substrate was prepared using photoreduction method. The synthesized MIL-101(Fe)@Ag composite substrate combines the localized surface plasmon resonance properties of silver nanoparticles and the high adsorption capacity of metal–organic frameworks. MIL-101 (Fe)@Ag composite substrate was characterized by FTIR, UV and SEM. The SERS activity of the composite substrates was characterized by measuring the Raman signals of PATP. The detection limit of the substrate for PATP was 10 –8  M, with a relative standard deviation of only about 5.3%, indicating good SERS effect and reproducibility of the substrate. Finally, the prepared substrate was applied for formaldehyde detection, with a detection limit of 10 –9  M. Principal component analysis was used for quantitative analysis of formaldehyde. This work proposes a simple method for synthesizing MIL-101(Fe)@Ag composite substrates with high SERS performance and uniformity and establishes a rapid detection method for formaldehyde using this substrate, which has great application prospects.

研究领域: 分析化学 · 纳米技术 · 材料科学 · 环境科学 · 光谱学
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