JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2018
·
IF 3.609
Ying Gong,Wenying Zhou,Zijun Wang,Li Xu,Yujia Kou,Huiwu Cai,Xiangrong Liu,Qingguo Chen,Zhi-Min Dang
In this work, graphene oxide (GO) nanosheets with surface modification by Tannic and Fe coordination complexes (TA-Fe) were incorporated into poly(vinylidene fluoride) (PVDF) to prepare high constant but low loss polymer nanocomposites , and the effect of TA-Fe interlayer on dielectric properties of the GO@TA-Fe/PVDF nanocomposites was investigated. The results indicate that the dosage, mixing ratio, and reaction time of TA-Fe complexes have obvious influences on the dielectric properties of the nanocomposites. Furthermore, the TA-Fe interlayer significantly influences the electrical properties of GO@TA-Fe nanoparticles and their PVDF composites, and the GO@TA-Fe/PVDF composites exhibit superior dielectric properties compared with raw GO/PVDF. Dielectric losses of the GO@TA-Fe/PVDF are significantly suppressed to a rather low level owing to the presence of TA-Fe layer, which serves as an interlayer between the GO sheets, thus preventing them from direct contacting with each other. Additionally, the dynamic dielectric relaxation of the GO/PVDF and GO@TA-Fe/PVDF nanocomposites was investigated in terms of temperature.
✓ 已验证
产品关联
DOI
高影响因子
Nanomaterials
·
2018
·Vol. 8
·期 4
·248
·
IF 3.504
Fuhua Wei,Ding Chen,Zhao Liang,Shuaiqi Zhao
Using a microwave-assisted ball-milling approach, Fe-based metal-organic frameworks (Fe-MOFs) were prepared from FeSO4·7H2O and trimesic acid. Scanning electron microscopy, Fourier-transform infrared spectrometry, X-ray, and thermogravimetric analysis were utilized to characterize the thermal stability and structure of the prepared Fe-MOFs. These Fe-MOFs were used to remove organic dyes from aqueous solutions. Specifically, they removed 96.97% of 23.3592 mg/L of Congo red in a 200 mL solution within 300 min of treatment with natural light at 15 °C. Likewise, 88.21 and 70.90% of 22.7527 mg/L of Orange II and 17.8326 mg/L of Rhodamine B, respectively, were removed from 200 mL solutions within 300 min of treatment at 15 °C. At 35 °C, 99.57, 95.98, and 99.38% of 23.3855 mg/L of Congo Red, 22.7365 mg/L of Orange II, and 17.9973 mg/L of Rhodamine B, respectively, were removed from 200 mL solutions within 300 min of treatment. The adsorption kinetics were investigated and the pseudo-first-order kinetic model was found to be superior to the pseudo-second-order kinetic model. Overall, using metal-organic frameworks to treat dye wastewater was found to be inexpensive, feasible, and efficient. Therefore, this material has future prospects in research and applications in the purification of wastewater.Keywords:wastewater treatment;metal-organic frameworks;dye removal;microwave-assisted ball milling
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2018
·
IF 4.439
Wen-Kun Gao,Jun-Feng Qin,Kai Wang,Kai-Li Yan,Zi-Zhang Liu,Jia-Hui Lin,Yong-Ming Chai,Chen-Guang Liu,Bin Dong
Cobalt sulfides have drawn enormous attention as earth-abundant alternatives to precious-metal electrocatalysts capable of catalyzing oxygen evolution reaction (OER) in alkaline medium. Although significant progresses have been realized in the development of various composite modulation to improve their properties for oxygen evolution, to boost their poor catalytic activity for oxygen evolution reaction is still challenging, which unambiguously limits the wide utilization of cobalt sulfides. Here, we present the facile growth of metal-doping (Fe, Ni) into Co 9 S 8 supported on nickle foam (NF) through a one-step simple hydrothermal process. The effect of (Fe, Ni)-doping on the morphology and the catalytic activity of Co 9 S 8 has been thoroughly investigated. Fe-Co 9 S 8 nano-microspheres supported on NF (Fe-Co 9 S 8 NM/NF) have been obtained with the remarkable electrocatalytic activity, which only requires a lower overpotential of 270 mV to reach a current density of 10 mA cm −2 and exhibits the smaller Tafel slope of 70 mV dec −1 as well as robust stability. The excellent OER performance of Fe-Co 9 S 8 NM/NF could be attributed to the synergistic interaction of Fe dopants with Co 9 S 8 nano-microspheres and faster charge transfer rate derived from NF support. This work provides a new and effective way to design metal-doped Co 9 S 8 -based heterostructures supported on conductive support as efficient OER electrocatalysts.
✓ 已验证
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2018
·
IF 5.091
Changjian Li,Yueqi Wang,Xiaojie Zhang,Xueling Guo,Xiaoxuan Kang,Libo Du,Yang Liu
Carbon dots have attracted considerable attention in the field of biosensors and bioimaging because of their excellent optical performance and low toxicity. However, the cellular uptake of the reported carbon dots generally has a low efficiency, which limits their practical applications. In this study, we reported a novel red fluorescent sulfur and nitrogen co-doped carbon dots with small molecular phenylboronic acid tags (i.e. S, N-CDs-PBA). The S, N-CDs-PBA can be taken up rapidly by PC12 cells in twenty minutes and showed high sensitivity for the detection of Fe 3+ ions. The maximum emission wavelength is at 593 nm under the excitation of 550 nm. The absolute fluorescence quantum yield is 23% in water. The fluorescence can be effectively and selectively quenched by Fe 3+ ions and the linear response range of Fe 3+ ions was obtained from 0.3 µM to 5.0 µM with a detection limit as low as 0.1 µM. It could be concluded that the rapid uptake of S, N-CDs-PBA into cells and high photoluminescence quantum yield of red emission are beneficial for quick detection of Fe 3+ ions.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ELECTROCHIMICA ACTA
·
2018
·
IF 5.116
Kelong Ao,Dawei Li,Yixin Yao,Pengfei Lv,Yibing Cai,Qufu Wei
Heteroatom doping is a feasible approach to adjust catalytic performance of the HER catalysts. In this work, we report a design of Fe-doped Co 9 S 8 nanosheets grown on carbon cloth (Fe-Co 9 S 8 NSs/CC) as a hydrophilic 3D monolithic electrocatalyst for efficient hydrogen evolution under all pH. The water contact angle and electrochemical measurements proved that the resultant material was hydrophilic for its nano hierarchitectures and dopant Fe enhanced the catalytic capability of singular Co 9 S 8 . In 1.0 M KOH, the Fe-Co 9 S 8 NSs/CC possessed a relatively small Tafel slope (95.3 mV dec −1 ) and required the overpotential of 83 mV to achieve 10 mA cm −2 . To drive the same current density, the overpotentials were 65 and 192 mV in 0.5 M H 2 SO 4 and 1.0 M PBS, respectively. Meanwhile, it showed good cycle stability and durability over 20 h static test at alkaline and neutral condition. The flexible freestanding catalyst has great potential in practical applications.
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Yangke Long,Yixuan Huang,Huiyi Wu,Xiaowen Shi,Ling Xiao
In this study, Fe-N-codoped carbonaceous catalysts (Fe-N-C-x) with different structures including one-dimensional carbon nanotubes (1D CNTs) and two-dimensional porous carbon sheets (2D NC) to three-dimensional carbon nanotubes/porous carbon sheets composites (3D CNTs/NC) were systematically synthesized and applied as peroxymonosulfate (PMS) activators. It was found that the Fe-N-C-x catalysts exhibited structure-dependent catalytic performance, following the order of 2D NC > 3D CNTs/NC > 1D CNTs, and also substrate-dependent degradation performance that the reaction kinetics varied greatly for different organic pollutants. Benefiting from the unique structure characteristic and high density of active sites, 2D Fe-N-C-1 showed far superior catalytic performance than the generally used carbocatalysts with negligible Fe leaching. Besides, various influential factors affecting the catalytic performance were systematically investigated. Fe-N-C-1 showed high catalytic efficiencies toward a broad spectrum of organic pollutants, and it was confirmed that both radical and non-radical degradation pathways existed during pollutants degradation. The competitive radical quenching tests and electron paramagnetic resonance measurements verified that the superoxide anion radical ( Â O 2 Â · - ) was the primary reactive oxidized species for degradation of p -chlorophenol (4-CP). The chronoamperometry analysis demonstrated that Fe-N-C-1 facilitated the electron transfer from 4-CP to PMS, resulting in the degradation of 4-CP through a non-radical mechanism. Our result not only reveals the structure-dependent PMS activation performance of transition-metal and nitrogen codoped carbocatalysts but also provides solid evidence that the defect-rich carbon materials with amorphous carbon and partial graphitic structure also favor the electron transfer mechanism.
✓ 已验证
产品关联
DOI
高影响因子
ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY
·
2018
·
IF 2.776
Chen Zhou,Huiqing Wang,Youbin Si,Kang Wu,Amina Yousaf
The ability of anthraquinone-2,6-disulfonate (AQDS) and riboflavin to enhance the sulfamethoxazole (SMX) degradation coupled with the Fe(III) reduction by Shewanella oneidensis MR-1 was investigated. The results indicated that the SMX degradation rate was 38.5% with an initial SMX concentration at 0.04 mM. For the overall performance of AQDS and riboflavin mediated SMX degradation and iron reduction, the SMX degradation rate was gradually increased with the enhancement of iron reduction. Riboflavin had a stronger enhancement on SMX degradation and iron reduction than AQDS, but the enhancement was not positively correlated with electron shuttles concentration. A quantitative characterization of the electron transfer capacity (ETC) of the electron shuttles showed that the ETC was higher for riboflavin than AQDS. The S. oneidensis MR-1 16S rRNA gene copies results indicated that electron shuttles had a positive effect on the microbial activity of S. oneidensis MR-1. The LC MS result indicated that the products of the SMX biodegradation were 3-amino-5-methylisoxazole and 4-aminobenzenesulfonic acid, which suggested that the SMX biodegradation was caused by S N bond cleavage. This study indicates that the biochemical mechanisms play a vital role in SMX transformation and Fe(II) generation in this system.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ACS Applied Energy Materials
·
2018
·
IF 0
Bao-Xia Dong,She-Liang Qian,Fan-Yan Bu,Yi-Chen Wu,Li-Gang Feng,Yun-Lei Teng,Wen-Long Liu,Zong-Wei Li
Heterogeneous electrocatalysis provides better control of the chemical surroundings of the catalyst’s active site for improved performance, offers the possibility of overcoming drawbacks of deactivation caused by aggregation or dimerization in homogeneous condition, and permits the use of benign aqueous solutions. Employing metal–organic frameworks (MOFs) or covalent–organic frameworks (COFs) to support the active molecular catalyst of porphyrin for electrochemical conversion of CO2 to CO is a promising strategy. We have rationally introduced a 3D highly stable porphyrin-based MOF of PCN-222(Fe) into heterogeneous catalysis through the simple dip-coating method. The composite catalyst PCN-222(Fe)/C (mass ratio = 1:2) exhibited high catalytic performance for electrochemical conversion of CO2 to CO with 494 mV overpotential (where j = 1.2 mA cm–2) and maximum 91% FECO in a CO2-saturated 0.5 M KHCO3 aqueous solution, achieving a TOF of 0.336 site–1 s–1. The catalyst was found to retain its crystallinity and stability after 10 h of electrolysis at −0.60 V versus RHE (average FECO 80.4%; RHE, reversible hydrogen electrode), which generates 334 μmol of CO with the TOF of 0.012 s–1 (0.286 site–1 s–1). These results indicate that the PCN-222(Fe)/C has a substantial catalytic effect on the electrochemical reduction of CO2 due to the combination of the intrinsic activity of the porphyrin molecule, and the promising CO2 adsorption ability endowed by the conserved porosity, as well as the high conductivity of carbon black.
✓ 已验证
产品关联
DOI
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2019
·
IF 4.084
Huiming Li,Yang Wang,Wei Zhu,Zhongbin Zhuang
Searching for low-cost electrocatalysts with high activity towards the hydrogen evolution reaction (HER) is of great significance to enable large-scale hydrogen production via water electrolysis . In this study, by using inverse spinel MFe 2 O 4 (M = Mn, Fe, Co, Cu) nanoparticles (NPs) as the precursors, monodisperse bimetallic phosphide M-Fe-P NPs/C with hollow structures were readily obtained by a gas-solid annealing method. These hollow phosphide NPs displayed excellent HER activity in an acidic medium with a low loading amount of 0.2 mg cm −2 . In particular, the Co–Fe–P NPs/C shows highest HER activity that only requiring an overpotential of 97 mV to retain a current density of 10 mA cm −2 . A volcano relation between activity and incorporated elements was revealed. Incorporation of cation with high electronegativity stabilized the FeP active centres, while phase segregation resulted in the loss of activity for Cu–Fe–P NPs/C.
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Jizhi Zhou,Pei Liu,Zeyuan Liu,Jia Zhang,Xin Huang
The recovery of phosphorus (P) from wastewater has attracted substantial attention with the atrophy of global P resource. In the current work, the simultaneous recovery of P with the removal of nickel (Ni) via iron/activated carbon (Fe/AC) and hydrogen peroxide (H 2 O 2 ) form nickel-plating wastewater was achieved. The isotherm reaction showed a maximum P recovery of 99.99% with an equilibrium concentration of P of 0.12 mg/L, which was lower than the limitation of discharge regulation (China national regulation, 0.5 mg/L). The optimal conditions for P recovery were 0.25 mol/L H 2 O 2 , a Fe/AC mass ratio of 1:1, an at 60 °C, which led to the ratio of P in the form of FePO 4 in the residue to be 77%. Moreover, the Fe/AC microelectrolysis coupling to H 2 O 2 promoted Fe 2+ production from Fe 0 and improved the circulation of Fe 2+ , which improved the production of hydroxyl radicals with increasing pH and consequently enhanced oxidation efficiency of hypophosphite. The FePO 4 was found the major form of phosphate in the precipitate. The highest removal rate of nickel was 89%, which was attributed to its precipitation at high pH and adsorption on to iron hydroxides and activated carbon. Nickel purification was achieved by further coagulation as the equilibrium concentration of Ni was lower than 0.1 mg/L. Therefore, our work provides a promising approach for simultaneous recovery of P and removal of Ni from electroplating wastewater.
✓ 已验证
产品关联
DOI
高影响因子
ADVANCED FUNCTIONAL MATERIALS
·
2019
·Vol. 29
·期 36
·1904056
·
IF 15.621
Jing Zhu,Chengchao Chu,Dongsheng Li,Xin Pang,Huili Zheng,Junqing Wang,Yesi Shi,Yang Zhang,Yi Cheng,En Ren,Jingliang Cheng,Xiaoyuan Chen,Gang Liu
To address the urgent need for effective sonodynamic therapy (SDT), a facile and efficient strategy is developed for fabricating a new class of sonotheranostics. Herein, a Fe(III)-porphyrin nano-sonosensitizer is prepared by a one-step coordination synthesis, and then anchored with Bis(DPA-Zn)-RGD and manganese superoxide dismutase (SOD2) siRNA. Benefiting from the delicate interactions of the Fe(III)-coordinated nanoformulations, a highly potent sono/gene combinational therapy guided by fluorescence/magnetic resonance imaging is achieved. Importantly, this sonotheranostics significantly enhances the SDT effect of porphyrin through the cancer-targeted delivery capability and enhanced reactive oxygen species production via triple-regulated approaches, including down-regulation of SOD2, depletion of glutathione, and generation of Fenton reaction. This work opens up new perspectives for developing versatile sonotheranostics to overcome the clinical challenges of SDT.
✓ 已验证
产品关联
DOI
高影响因子
Journal of Inorganic and Organometallic Polymers and Materials
·
2017
·Vol. 28
·期 3
·1299-1304
·
IF 1.577
Xiao He,Zhang Weibo,Wei Yicui,Yu Lubin,Chen Lihui
In this study, Fe/ZnO composite nanosheets were successfully prepared by hydrothermal method using nanofibrillated cellulose (NFC) as a soft template. The crystalline and morphology structure of the samples were characterized by X-ray diffraction (XRD), BET analysis, Scanning electron microscopy (SEM) and Transmission electron microscope (TEM). Fe doping not only fabricated ZnO from square to strip shape, but also brought larger surface area and pore volume, resulting 59.7% removal of tetracycline by adsorption action. UV–Vis absorption test, X-ray photoelectron spectroscopy (XPS) and Energy dispersive spectrometer (EDS) have shown that iron had successfully embedded into the ZnO nanosheets resulting in red-shift of absorption wavelength. Fe/ZnO nanocomposites had about 90% photodegradation for tetracycline after two hours’ UV-irradiation.
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）