SENSORS AND ACTUATORS B-CHEMICAL
·
2020
·
IF 7.1
Hao Liu,Huan Wang,Lu Zhang,Yanjuan Sang,Fang Pu,Jinsong Ren,Xiaogang Qu
Since excess fluoride ions may lead to a severe health hazard, it is imperative to design a facile and sensitive sensor to detect it in both environmental and biological systems. The reported methods are always subjected to some limits, hampering their practical application. Herein, a two-dimensional turn-on fluorescent sensor, Fe 3+ -integrated oxidized graphitic-phase carbon nitride nanosheets (Fe-g-CNO), was synthesized via a facile and green method for sensitive detection of fluoride ions. The interactions between the C-N/C = N moieties of oxidized graphitic-phase carbon nitride (g-CNO) and Fe 3+ caused fluorescence quenching of g-CNO. Upon addition of F- ions, the fluorescence was recovered through the formation of complex of Fe 3+ and F-. The limit of detection of the sensor was 1 × 10 -6 M. Furthermore, this probe could be used as an imaging agent of fluoride ions in living cells and teeth for diagnosis of dental fluorosis. The work provides a safe and efficient platform for further environmental and biomedical uses.
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DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2021
·
IF 5.816
Zhaoxu Li,Xinyi Luo,Meifang Luo,Yuan Qin,Chaozhong Guo,Yao Liu,Zhongli Luo
To design inexpensive carbon catalysts and enhance their oxygen reduction reaction (ORR) activity is critical for developing efficient energy-conversion systems. In this work, a novel Fe-N-C hybrid electrocatalyst with carbon nanolayers-encapsulated Fe 3 O 4 nanoparticles is synthesized successfully by utilizing the molecular-level confinement of graphitic C 3 N 4 structures via hemin biomaterial. Benefiting from the Fe-N structure prevalent on the carbon nanosheets and large mesopore-dominated specific surface area, the synthesized catalyst under optimized conditions shows excellent electrocatalytic performance for ORR with an E ORR at 1.08 V versus reversible hydrogen electrode (RHE) and an E 1/2 at 0.87 V vs. RHE, and outstanding long-term stability, which is superior to commercial Pt/C catalysts (E ORR at 1.04 V versus RHE and E 1/2 at 0.84 V versus RHE). Moreover, the low hydrogen peroxide yield (<11%) and average electron transfer number (~3.8) indicate a four-electron ORR pathway. Besides, the maximum power density of the home-made Zn-air battery using the obtained catalyst is 97.6 mW cm −2 . This work provides a practical route for the synthesis of cheap and efficient ORR electrocatalysts in metal-air battery systems.
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高影响因子
ENERGY & FUELS
·
2020
·
IF 3.421
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.
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DOI
高影响因子
TEXTILE RESEARCH JOURNAL
·
2023
·
IF 2.3
Limeng Yang,Wenqiang Yang,Chengyu Fu,Yujuan Li,Pengfei Zhang
This study simulated actual dyeing wastewater in dyeing factories with three types of dyeing wastewaters from laboratory cotton fabric dyeing to investigate the effects of catalyst and oxidant peroxymonosulfate (PMS) concentrations, pH level, and temperature on dye degradation in wastewater and determine the optimal conditions for dyeing wastewater treatment accordingly. The results demonstrated that the optimal conditions varied with the reactive dyes. Specifically, the optimal oxidant PMS concentration for degrading Reactive Yellow and Reactive Blue was 0.6 g/L, and that for degrading Reactive Red was 0.4 g/L. The optimal pH level for degrading Reactive Red and Reactive Blue was around 7.0, and that for degrading Reactive Yellow was about 5.0. The activation energy of the degradation and the mineralization degree of the three dyes were also discussed. Reactive Blue showed greater activation energy (47.0 kJ/mol) and a higher mineralization degree (81% chemical oxygen demand removal) than the other two dyes under optimal disposal conditions. The Fe/N-codoped carbocatalyst loaded on carbon cloth exhibited desirable reusability and good stability for the degradation of the three dyes. Mechanisms involved in their degradation were analyzed through X-ray photoelectron spectroscopy, focusing on N species, Fe-N binding, and C=C and C–N active components in the Fe/N-codoped carbocatalyst. Electron paramagnetic resonance experiments demonstrated that both the radical and non-radical pathways were accountable for the degradation of the three dyes, primarily the non-radical pathway. This study may contribute to the application of activated PMS for practical dyeing wastewater treatment.
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DOI
高影响因子
Environmental Science-Nano
·
2019
·Vol. 6
·期 9
·2850-2862
·
IF 7.704
Xiaoyu Bai,Yi Li,Liangbo Xie,Xiaohui Liu,Sihui Zhan,Wenping Hu
Antibiotics accumulate because of their extensive use and difficult degradation, which can lead to the formation of novel antibiotic resistant genes and bacteria, which can cause damage to human health and the ecological environment. Here, we designed a novel photo-electro-Fenton-like (PEF-like) system with bifunctional Z-scheme WO3/g-C3N4 for accelerated decomposition and enhanced mineralization of stubborn ciprofloxacin (CIP). This PEF-like system, accompanied by visible light activation, with the optimal WO3/g-C3N4 (1 : 6) composite exhibited outstanding removal efficiency of CIP compared with a single photocatalysis system and electro-Fenton-like (EF-like) system, and the elimination rate reached 100% within 2 h under visible light irradiation. The WO3/g-C3N4 (1 : 6) composite displayed the strongest visible light absorption, the weakest recombination of electron–hole pairs, the highest photocurrent response and the lowest electrochemical impedance compared with pristine WO3 and g-C3N4. Significantly, WO3/g-C3N4 (1 : 6) played a dual role in the PEF-like system which could not only produce ˙OH, ˙O2− and h+ during photocatalysis, but could also generate ˙OH through the reactions of W5+ and photoexcited electrons of g-C3N4 for the decomposition of H2O2. It was worth noting that this bifunctional PEF-like catalyst with photoelectric synergy could replace Fe2+ in a conventional electro-Fenton reaction and the pH range was broadened while still maintaining efficient degradation efficiency in the range of 2–9. The PEF-like system maintained a high elimination rate of CIP after five consecutive runs which revealed that it possessed prominent stability and feasibility.
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DOI
高影响因子
RSC Advances
·
2017
·Vol. 7
·期 80
·50829-50837
·
IF 3.108
Juntao Tang,Jianlong Wang
A MIL-100(Fe)/graphene oxide (GO) composite was prepared by a one-step hydrothermal method and utilized as a heterogeneous Fenton-like catalyst for methyl orange (MO) degradation. The obtained catalyst was characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), nitrogen adsorption–desorption isotherms, thermogravimetric (TG) analysis, X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FTIR). The effects of H2O2 dosage, initial pH and catalyst dosage on the degradation of MO were investigated. The MIL-100(Fe)/GO presented high catalytic activity for the degradation of MO, achieving almost complete decomposition of MO after 240 min with reaction conditions of 8 mM H2O2, pH of 3.0 and 0.5 g L−1 catalyst. Kinetics analysis showed that MO removal followed a pseudo-first-order kinetic model. The catalyst showed stable catalytic activity and reusability after three successive runs. The possible catalytic mechanism of MIL-100(Fe)/GO was also proposed.
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DOI
高影响因子
Journal of Materials Chemistry B
·
2014
·Vol. 2
·期 37
·6306-6312
·
IF 0
Fangyuan Gai,Xiang Li,Tianlei Zhou,Xiaogang Zhao,Dongdong Lu,Yunling Liu,Qisheng Huo
This work demonstrates a luminescent chemosensor based on silica cross-linked micellar nanoparticles (SCMNPs) designed by encapsulating a phenothiazine-derived Schiff base, (4E)-4-((10-dodecyl-10H-phenothiazin-7-yl)methyleneamino)-1,2-dihydro-1,5-dimethyl-2-phenylpyrazol-3-one (EDDP), for the selective detection of Fe3+. The encapsulation of EDDP inside SCMNPs (EDDP–SCMNPs) can avoid the metal (Fe3+/Fe2+)-promoted hydrolysis of EDDP and, thus, exhibit highly selective determination of Fe3+. The electron transfer (ET) from EDDP in the core to Fe3+ adsorbed on the shell of EDDP–SCMNPs was verified using UV-vis absorption, fluorescent emission and 3D fluorescence spectra. Moreover, EDDP–SCMNPs showed no sensing ability of Fe2+ due to the weak electron-accepting ability of Fe2+. Significantly, because of their ultrasmall size, nontoxicity, good water solubility and biocompatibility, EDDP-SCMNPs have potential applications in biological systems.
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DOI
PubMed
Materials
·
2023
·Vol. 17
·期 1
·6
·
IF 3.4
Yu Lei,Hongdian Chen,Chenyang Shu,Changguo Chen
Developing catalysts with superior activity to hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is equally important to the overall photoelectrochemical water splitting to produce hydrogen. In this work, bismuth oxyiodide (BiOI), iron-modified bismuth iodide Fe/BiOI, and the sulfurized S-Fe/BiOI were prepared using the solvothermal method. The three materials all have good absorption ability for visible light. The photoelectrochemical catalytic activity of BiOI to oxygen evolution reaction (OER) is significantly enhanced after iron modification, while the sulfurized product S-Fe/BiOI exhibits better catalytic activity to hydrogen evolution reaction (HER). Hence, OER and HER can be simultaneously catalyzed by using Fe/BiOI and S-Fe/BiOI as anodic and cathodic catalysts to facilitate the overall photoelectrochemical water splitting process.Keywords:bismuth oxyiodide;iron modification;sulfurization;overall water splitting;photoelectrochemical catalysis
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DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2022
·
IF 10.383
Zixia Tang,Hong Tao,Xiao Wang,Lu Chen,Chi Song,Guanhong Lu,Xiaofeng Xie,Jing Sun
The implantation of metal nanoparticles (MNPs) into metal–organic framework (MOF) hosts is a promising means to prepare high-performance photocatalysts for the degradation of gas pollutants. However, the uniform encapsulation of MNPs in MOFs is still challenging. Herein, a facile “quasi-in situ” encapsulation method is proposed by utilizing the spatial confinement effect of the colloidal network formed during the synthesis of the MIL-100(Fe) monolith [noted as m-MIL-100(Fe)]. Highly dispersed Ag NPs with an average diameter of ∼2 nm are encapsulated in the MIL-100(Fe) monolith to form a unique “watermelon-seed” structure, which ensures the large contact area between the two components and protects Ag NPs from being oxidized. The fast charge transfer between m-MIL-100(Fe) and Ag NPs enables the spatial separation of electron–hole pairs and promotes the generation of oxidative radicals. Compared with pristine m-MIL-100(Fe), the 0.2 wt % Ag@m-MIL-100(Fe) composite shows obviously enhanced photodegradation efficiencies for flowing o-xylene under both xenon (∼97%) and visible light (∼80.0%) with high stability. This work not only provides a promising Ag@m-MIL-100(Fe) material for eliminating air pollutants but also gives a versatile means for the design and synthesis of nanoparticles@MOFs composites with desired performance.
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DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Pengfei Wan,Siyang Dong,Jing Xiong,Xuanyang Jin,Shengjun Lu,Yufei Zhang,Haosen Fan
Lithium sulfur batteries (LSBs) have been considered as one of the most promising options for next generation high-performance batteries. However, the heavy shuttle effect and inferior redox conversion during the charge/discharge processes of the batteries have greatly hindered their further applications. In this study, to address these disadvantages of LSBs, Fe/Fe 3 C/FeN 0.0324 heterostructured nanocubes were designed and prepared through high temperature carbonization process using Prussian blue precursor. Then the Fe/Fe 3 C/FeN 0.0324 nanocubes were used to modify the commercial polypropylene (PP) separator, which can greatly catalyze the redox transformation of polysulfides and provide sufficient active sites for chemisorption . As result, the modified separator endowed LSBs with excellent rate capacity and cycle stability, delivering a high-capacity of 1025 mAh/g at 0.5 C with nearly 100% coulombic efficiency. It also displayed a superb cycling performance with a per-cycle capacity attenuation rate of 0.09% after 300 cycles. When the current density increased to 1 C with the S loading of 1.73 mg cm −2 , Fe/Fe 3 C/FeN 0.0324 -PP separator presented a satisfactory capacity decay rate of 0.05% per cycle after 1000 cycles. Besides, it also presented outstanding electrochemical performance even at high sulfur loading of 4.5 mg cm −2 . This work has provided a new avenue for the design of nanomaterials with synergistic effect of catalytic conversion and chemisorption of polysulfides for the promotion of high-performance Li-S batteries.
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DOI
PubMed
高影响因子
Nanoscience and Nanotechnology Letters
·
2019
·Vol. 11
·期 9
·1263-1270
·
IF 0
Li Zhanguo,Shi Chao,Wang Lijuan,Sun Lijing,Sun Qiang
Photocatalytic nanocomposites of titanium dioxide (TiO2) were prepared by hydrothermal method. Reduced graphene oxide (RGO) was applied to prepare various TiO2 composites of doped nanoparticles by using NH4Cl and FeCl3 as sources. The structure
and morphology of these composites showed that TiO2 was loaded on surface of RGO. Meanwhile, the agglomeration of TiO2 decreased and the dispersion became uniform for doped materials. Under ultraviolet (UV) light irradiation, the photocatalytic degradation of volatile
organic compounds (VOC) by RGO/TiO2 composites with codoping of N and Fe reached to 90.5%. The photocatalytic degradation was higher than RGO/TiO2 composites and pure TiO2 by 1.8 and 5.9 times, respectively. The role of co-doping composites may have a possible
mechanism for toluene under UV light irradiation. The enhanced photocatalytic properties were attributed to N and Fe doping which generated intermediate energy level, extended absorption and decreased band gap of UV light.
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DOI
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2021
·
IF 8.067
Kun Li,Luxin Liang,Peng Du,Zeyun Cai,Tao Xiang,Hiroyasu Kanetaka,Hong Wu,Guoqiang Xie
Magnesium (Mg) alloys can be regarded as the most promising biodegradable implant materials for orthopedic and stent applications due to their good biocompatibility and low Young's modulus which is near to that of natural bone. However, its applicability is hindered because it exhibits a high corrosion rate in the physiological environments. In this work, we fabricated Mg 66 Zn 30 Ca 4 /Fe bulk metallic glass composites via spark plasma sintering (SPS). We studied the influence of different contents of Fe on the properties of the composites. The results indicated that Fe was uniformly distributed on the surface of Mg 66 Zn 30 Ca 4 metallic glass (MG) as a second phase, which led to an improvement in the corrosion resistance and mechanical strength. The standard potential of Mg 66 Zn 30 Ca 4 /Fe bulk metallic glass (BMG) composites increased as compared to Mg 66 Zn 30 Ca 4 , while their mechanical strength improved from 355 MPa to 616 MPa. Furthermore, cytotoxicity was investigated via the CCK-8 assay and calcein-AM staining, which revealed that the extraction mediums diluted 6 times (EM × 6) of the Mg 66 Zn 30 Ca 4 and Mg 66 Zn 30 Ca 4 /Fe did not cause cell toxicity on day 3 and 5, while the EM × 6 of the Mg 66 Zn 30 Ca 4 showed cytotoxicity on day 1, 3 and 5. Thus, Mg 66 Zn 30 Ca 4 /Fe BMG composites exhibit significant potential for fabricating implants with good mechanical strength and corrosion resistance.
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高影响因子
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