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APPLIED CATALYSIS B-ENVIRONMENTAL · 2021 · IF 19.503

Exposing highly active (100) facet on a SnS2/SnO2 electrocatalyst to boost efficient hydrogen evolution

Jing Wu,Rong Zhao,Hui Xiang,Chenfan Yang,Wenda Zhong,Chengzhi Zhang,Qin Zhang,Xuanke Li,Nianjun Yang

Tin disulfide (SnS 2 ), one transition metal dichalcogenide (TMD) is a cost-effective and promising electrocatalyst for hydrogen evolution reactions (HER) in the alkaline electrolytes. Its electrocatalytic HER performance is unfortunately limited, originating from its un-conspicuous inherent catalytic activities and non-favorable adsorption sites for hydrogen. Herein, a tin disulfide/stannic oxide (SnS 2 /SnO 2 ) heterostructure is designed and grown on the nickel foam (denoted as SnS 2 /SnO 2 -NF). The SnS 2 /SnO 2 heterostructure introduces more active (100) facets or a high density of active sites, accelerates the diffusion kinetic of electrons and ions, lowers the water dissociation energies, and optimizes adsorption energies of hydrogen atoms. On this catalyst, superior HER performance is realized in an alkaline medium. An overpotential of 108 mV at a current density of −10 mA cm –2 with a Tafel slope of 50.1 mV dec –1 and long-term durability are achieved for HER in 1 M KOH. This work paves a new way to design high-performance HER electrocatalyst through facet engineering of the designed heterostructures.

研究领域: 材料科学 · 电化学
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Desalination and Water Treatment · 2024 · IF 1

Adsorption of neutral red onto MIL-100(Fe) from solution: characterization, equilibrium, kinetics, thermodynamics and process design

Shanshan Chen,Kang Wen,Xiaoting Zhang,Ruize Zhang,Runping Han

Metal organic frameworks are attracting scientific interest in adsorption applications owing to their large surface area and controllable pore size or shape over both microporous and mesoporous domains. Based on this, an iron(III) trimesic acid MIL-100(Fe) was facilely synthesized by hydrothermal treatment and used as adsorbent to remove neutral red (NR) from aqueous solution. MIL-100(Fe) was characterized using X-ray diffraction, scanning electron microscopy and transform infrared spectroscopy. MIL-100(Fe) was studied in view of the adsorption isotherms, thermodynamics, kinetics, and regeneration of the adsorbent. The adsorption kinetics data of NR were found to be in agreement with pseudo-second-order model. Temkin model was observed to be more suitable than Freundlich and Langmuir models in describing the adsorption isotherm. The maximum adsorption quantity was 333 mg g –1 at 313 K from Langmuir model. Thermodynamic parameters indicated that the NR adsorption process was endothermic and spontaneous. The NR-loaded MIL-100(Fe) adsorbent was regenerated and reused using pH = 2, 75% ethanol. A single-stage batch design for NR adsorption onto MIL-100(Fe) was also presented based on Temkin isotherm model equation. Based on the findings, MIL-100(Fe) is a promising adsorbent for the removal of cationic dyes from solution and thus can be used in practical application.

研究领域: 环境科学 · 材料科学 · 化学工程
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RSC Advances · 2017 ·Vol. 7 ·期 10 ·5621-5627 · IF 3.108

MIL-100(Fe)-catalyzed efficient conversion of hexoses to lactic acid

Shan Huang,Kai-Li Yang,Xiao-Fang Liu,Hu Pan,Heng Zhang,Song Yang

MIL-100(Fe) was used for the first time in the catalytic transformation of hexose sugars into lactic acid (LA). The as-synthesized MIL-100(Fe) was systematically characterized, and its superior morphological and textural properties were demonstrated to contribute greatly to the pronounced catalytic performance in fructose-to-LA conversion (up to 32% yield), as compared with other catalysts like Cu-BTC and MIL-100(Cr). The effects of reaction conditions including temperature, reaction time, and substrate loading were explored. In addition, MIL-100(Fe) could be easily reused for 4 cycles with no evident decrease in catalytic activity.

研究领域: 化学工程 · 催化 · 生物化学
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Water Reuse · 2024 ·Vol. 14 ·期 1 ·39-50 · IF 4.3

Removal of tellurium(IV) from environmental aquatic systems using metal-organic framework material MIL-100(Fe)

Huang Yiru,Li Youyou,Zhong Qingwei,Luo Chen

View large Download slide View large Download slide Close modal Metal-organic framework (MOF) materials, characterized by their porosity and large specific surface areas, exhibit excellent adsorption properties. With the aim of removing Te(IV) from environmental aquatic systems, this study is the first to propose the use of MIL-100(Fe). The material reveals a strong adsorption capacity for Te(IV), with maximum adsorption of 531.9 mg/g, superior to other adsorbent materials. Adsorption isotherm and kinetic models indicate that the adsorption process primarily involves monolayer chemical adsorption. According to the thermodynamic parameters, the adsorption reaction is endothermic. The experiment individually examined factors affecting the material's adsorption performance, including adsorbent dose, initial concentration of Te(IV), pH, adsorption time, and coexisting ions. Even under high ion strength conditions and high concentrations of coexisting ions, the material's adsorption efficiency for Te(IV) still reached over 94%. The material has been successfully applied to remove Te(IV) from lake water, river water, and seawater, yielding satisfactory results. Due to the high salinity and ionic strength of the solution, the removal efficiency of Te(IV) in the seawater matrix was slightly lower than that in freshwater (river and lake water). Thus, this material shows promise for the removal of Te(IV) from complex aquatic systems. MIL-100(Fe) was prepared and characterized. The Te(IV) can be adsorbed by MIL-100(Fe) effectively, and the adsorption process was primarily a monolayer chemical adsorption and an endothermic reaction. The Te(IV) can be removed effectively in environmental water supplies by MIL-100(Fe).

研究领域: 环境科学 · 材料科学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2021 · IF 5.816

Improved room-temperature hydrogen storage performance of lithium-doped MIL-100(Fe)/graphene oxide (GO) composite

Chengbao Liu,Dongchen Shen,Zhengkai Tu,Song Li

Li + doping is regarded as an effective strategy to enhance the room-temperature hydrogen storage of metal-organic frameworks (MOFs). In this work, Li + is doped into both MIL-100(Fe) and MIL-100(Fe)/graphene oxide (GO) composite, and it is demonstrated that the hydrogen uptake of Li + doped MIL-100(Fe)/GO (2.02 wt%) is improved by 135% compared with Li + doped MIL-100(Fe) (0.86 wt%) at 298 K and 50 bar, which is ascribed to its higher isosteric heat of adsorption (7.33 kJ/mol) resulting from its more accessible adsorption sites provided by doped Li + ions and ultramicropores. Grand canonical Monte Carlo (GCMC) simulation reveals that Li + ions distributing in the interface between MIL-100(Fe) and GO within MIL-100(Fe)/GO composite is favorable for hydrogen adsorption owing to the increased number of adsorption sites, thus contributing to the enhanced hydrogen storage capacity. These findings demonstrate that MIL-100(Fe)/GO is a more promising Li + doping substrate than MIL-100(Fe).

研究领域: 材料科学 · 能源化学
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MICROCHIMICA ACTA · 2025 ·Vol. 192 ·期 3 ·1-10 · IF 5.3

Rapid determination of malachite green in fish by surface-enhanced Raman spectroscopy combined with MIL-100 (Fe)

Han Hongyu,Huang Yiqun,Miao Junjian,Lai Keqiang

Surface-enhanced Raman spectroscopy (SERS) was combined with stoichiometric analysis to synthesize a AuNPs@MIL-100 (Fe) SERS substrate. This high-performance, and low-cost metal–organic framework-based SERS nano sensor is capable of detecting malachite green (MG) residues in fish. The minimum detectable  concentration of MG in standard solutions is 0.1 μg/L, while in fish samples, the detection range spanned from 0.003–0.088 μg/kg. The partial least squares regression (PLSR) and support vector machine regression (SVR) were applied to model the SERS data, enhancing both the precision and reliability of the detection. The results show that compared with the traditional linear regression and PLSR models, the prediction accuracy of the SVR model is an  improvement with higher stability. MG standard solutions and three fish samples can  be analysed directly or after simple extraction. This method can be used to detect trace harmful substances in different aquatic products. Graphical

CAS / MDL: 7782-61-8
研究领域: 食品安全 · 分析化学 · 环境科学
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Surfaces and Interfaces · 2024 · IF 5.7

Boosting photothermal CO2 hydrogenation with H2O by MIL-100(Fe) derived Fe@C confined Ni2P

Pengfei Zhu,Mengrong Geng,Shuang Qin,Heyang Cao,Zhenhong He,Xinhua Gao,Chuanyi Wang

The conversion of CO 2 into chemical products or fuels of great value always remains an outstanding challenge. Here, we report a heterojunction Fe@C/Ni 2 P composite catalyst obtained by preparing MIL-100(Fe) derived Fe@C confined Ni 2 P nanoparticles, which is applied to photothermal catalytic CO 2 hydrogenation with H 2 O. Without adding any sacrificial agents or co-catalysts, the optimal Fe@C/Ni 2 P sample shows higher yields for CO 2 -to-C 2 H 6 and CO 2 -to-CO yield of 5.83 μmol g −1 h −1 and 179.9 μmol g −1 h −1 than that of pristine Fe@C and Ni 2 P, respectively. The experimental results indicated that the obtained Fe@C/Ni 2 P can act as catalytic sites to adsorb, activate, and convert CO 2 under low-intensity LED light irradiation (420 nm) with a temperature of 200 ℃. The physical structure, photochemical properties and energy band structure of the Fe@C/Ni 2 P composite catalysts were investigated by XRD, XPS, FT-IR, TEM, BET, respectively. Furthermore, the reaction pathway of Fe@C/Ni 2 P photothermal catalytic CO 2 hydrogenation with H 2 O to C2 products and CO were systematically analyzed by in situ infrared spectroscopy (DRIFTS).

CAS / MDL: 7723-14-0
研究领域: 化学 · 材料科学 · 环境科学
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JOURNAL OF MATERIALS CHEMISTRY · 2012 ·Vol. 22 ·期 15 ·7449-7455 · IF 5.968

Metal–organic framework MIL-100(Fe) for the adsorption of malachite green from aqueous solution

Shu-Hui Huo,Xiu-Ping Yan

The adsorption of malachite green from aqueous solution on a highly porous metal–organic framework MIL-100(Fe) was studied in view of the adsorption isotherm, thermodynamics, kinetics, and regeneration of the sorbent. The adsorption isotherms of malachite green on MIL-100(Fe) followed the Freundlich model, and MIL-100(Fe) possessed heterogeneous surface caused by the presence of different functional groups on the surface. The adsorption of malachite green on MIL-100(Fe) is controlled by an entropy effect rather than an enthalpy change, and obeyed a pseudo-second-order kinetics. Analysis of the intraparticle diffusion plots revealed that more than one process affected the adsorption, and film (boundary layer) diffusion controlled the adsorption rate at the beginning. Evidence from zeta potential and X-ray photoelectron spectroscopic data showed that the adsorption of malachite green was also driven by electrostatic attraction and the interaction between the Lewis base –N(CH3)2 in malachite green and the water molecule coordinated metal sites of MIL-100(Fe). MIL-100(Fe) gave much higher adsorption capacity for malachite green than other conventional adsorbents such as activated carbon and natural zeolite. The high adsorption capacity, good solvent stability, and excellent reusability make MIL-100(Fe) attractive for the removal of MG from aqueous solution.

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

One-step synthesis of magnetically recoverable AgCl/Fe3O4@MIL-100(Fe) for high-performance photocatalysis

Jun Liu,Hui Wang,Wen-Yao Zhu,Heng-Xue Xie,Xin Li,Wen-Juan Li,Ge Bai,Meng-Jie Chang,Xiao-Jiao Chai,Hui-Ling Du,Shi-Jie Song

We present a novel method to facilely prepare magnetically recoverable AgCl/Fe 3 O 4 @MIL-100(Fe) (ACFM) nanostructures for photocatalytic degradation of rhodamine B (RhB). The ACFM was directly prepared via a simple successive ionic layer adsorption and reaction (SILAR) deposition of MIL-100(Fe) on solvothermal synthesized Ag/Fe 3 O 4 nanoparticles , in which process Ag was completely oxidized into AgCl concurrent with the formation of MIL-100(Fe). The ACFM prepared with 15 SILAR cycles exhibits 92.9% efficiency towards photodegrading RhB within 30 min under visible light illumination, which is higher than that of the individual structure of AgCl/Fe 3 O 4 , Ag/Fe 3 O 4 @MIL-100(Fe) or Fe 3 O 4 @MIL-100(Fe). The remarkably enhanced photocatalytic performance is attributed to the abundant active sites and sufficient visible light response of MIL-100(Fe), as well as effective charge separation at the heterojunction interface between AgCl and MIL-100(Fe). Furthermore, the obtained ACFM can be quickly separated from the pollutant solution with a magnet and possesses good stability for recycling photocatalysis . In light of the study, the ACFM nanostructures are believed to be applied as promising photocatalysts for practical applications.

CAS / MDL: 554-95-0
研究领域: 材料科学 · 环境科学
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CRYSTENGCOMM · 2018 ·Vol. 20 ·期 41 ·6580-6588 · IF 3.304

Concave structure of Cu2O truncated microcubes: PVP assisted {100} facet etching and improved facet-dependent photocatalytic properties

Pengwei Li,Dingding Li,Lina Liu,Anli Li,Cuixian Luo,Yue Xiao,Jie Hu,Huabei Jiang,Wendong Zhang

In this work, a concave structure of Cu2O truncated microcubes with {100} facet erosion has been successfully synthesized by a facile top-down etching method. Air and PVP were employed as an etchant and a shape controller agent, respectively. For the facet-selective capping of PVP on Cu2O {111} planes, the traditional relatively low energy {100} facets of Cu2O truncated microcubes would be selectively etched along their [100] zone axis in a top-down manner. The {100} facet etched Cu2O concave truncated microcubes exhibited highly improved photocatalytic activities (2.15 and 1.21 times, respectively) compared to that of the basic structure and the {111} facet etched samples on the degradation of Congo red (CR), displaying distinct facet-dependent photocatalytic characteristics, excellent stability and reusability. This work not only builds an efficient photocatalyst, but also provides a novel method to fabricate a variety of architectures with low energy facets etched and highly active crystal planes exposed, which is extremely important for the improvement of catalytic activities.

CAS / MDL: 25249-54-1 9003-39-8
研究领域: 材料科学 · 化学工程 · 环境科学
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Journal of Composites Science · 2025 ·Vol. 9 ·期 5 ·250 · IF 3.7

Enhanced Photoelectrochemical Water Splitting Using a NiFe2O4/NG@MIL-100(Fe)/TiO2 Composite Photoanode: Synthesis, Characterization, and Performance

Waheed Rehman,Faiq Saeed,Samia Arain,Muhammad Usman,Bushra Maryam,Xianhua Liu

NiFe2O4and TiO2are widely studied for photoelectrochemical (PEC) applications due to their unique properties. Nitrogen-doped graphene (NG) and metal–organic frameworks (MOFs), such as MIL-100(Fe) (where MIL stands for Materials of Lavoisier Institute), are commonly incorporated to enhance PEC performance by offering a high surface area and facilitating efficient charge transport. Composite systems are commonly employed to overcome the limitations of individual PEC catalysts. In this study, a highly efficient NiFe2O4/NG@MIL-100(Fe)/TiO2photoanode was developed to enhance photoelectrochemical water-splitting performance. The composite was synthesized via a hydrothermal method with a two-step heating process. X-ray diffraction confirmed the expected crystal structures, with peak broadening in NiFe2O4indicating reduced crystallite size and increased lattice strain. X-ray photoelectron spectroscopy of the Ni 2p and Fe 2p regions validated the successful integration of NiFe2O4into the composite. Electrochemical analysis demonstrated excellent performance, with linear sweep voltammetry achieving a peak photocurrent density of 3.5 mA cm−2at 1.23 V (vs RHE). Electrochemical impedance spectroscopy revealed a reduced charge-transfer resistance of 50 Ω, indicating improved charge transport. Optical and electronic properties were evaluated using UV-Vis spectroscopy and Tauc plots, revealing a direct bandgap of 2.1 eV. The composite exhibited stable photocurrent under amperometric J-t testing for 2000 s, demonstrating its durability. These findings underscore the potential of NiFe2O4/NG@MIL-100(Fe)/TiO2as a promising material for renewable energy applications, particularly in photoelectrochemical water splitting.

研究领域: 材料科学 · 能源科学 · 电化学
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BRAZILIAN JOURNAL OF MICROBIOLOGY · 2021 ·Vol. 53 ·期 1 ·161-169 · IF 2.476

Enhanced antibacterial effect against Enterococcus faecalis by silver ions plus Triton X-100 with low concentrations and cytotoxicity

Duan Mengting,Sun Qing,Fan Wei,Fan Bing

Enterococcus faecalis ( E. faecalis ) is commonly considered to be one of chief culprits of secondary and persistent root canal infections. As antibiotic resistance has become a global issue, in order to reduce the use of antibiotics, metal ions have recently been widely used as an alternative. Silver ions (Ag + ) have been proved to be a strong bactericide but with high cytotoxicity and discoloration property. Triton X-100 (TX-100) and Ag + were co-used for the first time as a clinical intracanal medication to obtain both enhanced antibacterial effect and low cytotoxicity. The synergistic antibacterial effect of TX-100 + Ag + was tested on both planktonic and biofilm-resident E. faecalis on dentine. And the cytotoxicity was tested on MC3T3-E1 cells. Results confirmed the antibacterial activity against both planktonic and biofilm-resident E. faecalis was dramatically improved after TX-100 incorporation. TX-100 and Ag + mixture demonstrated a similar inhibitory effect as the 2% chlorhexidine (CHX), while the cytotoxicity was much lower than 2% CHX ( p  < 0.05). In conclusion, TX-100 + Ag + mixture might be developed into a new effective intracanal medication as the 2% CHX.

CAS / MDL: 9004-32-4 9085-26-1
研究领域: 口腔医学 · 微生物学
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