JOURNAL OF MATERIALS SCIENCE
·
2022
·Vol. 57
·期 46
·21402-21410
·
IF 4.682
Wang J.,Ou X. L.,Zhang J.,Chen X. Y.,Zhao K.,Yang X. S.,Zhao Y.
Fe(Te,Se) is a simple, iron-based compound that is conducive to the study of superconductivity mechanisms and has potential for large-scale applications. At present, Fe(Te,Se) thin films are primarily prepared using the pulsed laser deposition method. Herein, FeTe 0.6 Se 0.4 films were grown by magnetron sputtering on CaF 2 substrates. The effect of sputtering pressure on the superconductivity of the film was investigated. Excessive pressure caused a higher iron content, which affected the superconductivity and prevented it from completely reaching a zero-resistance state. Δ T c was smaller for the film grown under 0.2 Pa, and its upper critical field reached 144.35 T, which indicates its greater application potential. Our results illustrated that sputtering pressure was a critical process parameter, which provided an important reference for future research to fabricate commercial iron-based superconducting tapes by magnetron sputtering.
研究领域:
凝聚态物理
·
材料科学
·
超导材料
·
薄膜制备
·
应用物理学
✓ 已验证
DOI
高影响因子
CRYSTENGCOMM
·
2025
·Vol. 27
·期 5
·678-686
·
IF 2.6
Dongling Xie,Jianan Wang,Bo Huang,Yiyi Yang,Dunmin Lin,Chenggang Xu,Fengyu Xie
Rational design of viable routes to develop affordable and efficient oxygen evolution reaction (OER) catalysts is essential for advancing electrochemical water splitting, yet significant challenges remain, particularly in seawater. Here, we propose a ligand defect engineering strategy to modify the electronic structure of NH2-MIL-88B(Fe) using a monodentate ligand (acetic acid, AcOH), inducing ligand vacancies in NH2-MIL-88B(Fe) for oxygen evolution in an alkaline seawater electrolyte, thereby improving the performance of the electrocatalysts. The resulting defective MOFs (denoted as NH2-MIL-88B(Fe)-x) exhibited exceptionally high catalytic activity for OER, requiring low overpotentials of 313 and 329 mV at a current density of 100 mA cm−2 in 1 M KOH and simulated seawater (1 M KOH + 0.5 M NaCl) solutions, respectively. Experimental analyses revealed that the introduction of AcOH can modulate the d-band center of active sites in NH2-MIL-88B(Fe)-x and play a critical role in alleviating chloride ion (Cl−) corrosion, thereby enhancing catalytic stability in seawater. When directly used as an OER catalyst in an alkaline electrolyte, wind and solar power were harnessed to operate the NH2-MIL-88B(Fe)-x || Pt/C configuration to drive the electrolytic water reaction. Thus, the ligand defect strategy can be employed to design and prepare high-performance OER electrocatalysts, particularly for generating H2 through water electrolysis powered by renewable energy sources.
研究领域:
材料科学
·
电化学
·
能源工程
✓ 已验证
产品关联
DOI
高影响因子
ACS Catalysis
·
2025
·
IF 13.1
Ziyi Wang,Xin Lian,Rongyan Yang,Xiaomeng Guo,Shengjie Wei,Jijie Zhang,Xian-He Bu
Introducing polarity in traditional metal-N4 catalytic sites and strengthening the adsorption of polar NO2* intermediate are advantageous for the deep reduction of nitrate into ammonia. Herein, the planar chlorination engineering strategy successfully introduced the C–Cl bonds adjacent to the Fe–N4 catalytic site with higher polarity, effectively boosting the catalytic activity for the nitrate reduction reaction (NO3RR). The maximal NH3 yield rate and the corresponding turnover frequency (TOF) value catalyzed by the Fe–N4/CNCl catalyst were 1.82 mg h–1 cm–2 and 245 h–1 at −0.83 V vs RHE, which were 3.4 times and 2.7 times those of the traditional Fe–N4/CN catalyst without polarity, respectively. The Fe–N4/CNCl catalyst also exhibited satisfactory stability during consecutive 15 cycles. The density functional theory (DFT) calculation revealed that the planar chlorination engineering of the Fe–N4 site with higher polarity strengthened the adsorption of polar NO2* intermediate, facilitated the deep reduction of nitrate into ammonia, lowered the energy barrier of rate-determining step (RDS) and thus improved the catalytic activity. This work exhibited the enormous advantage of a planar chlorination engineering strategy for enhancing the activity of electrocatalysis by introducing polarity in the traditional metal-N4 catalytic site.
研究领域:
材料科学
·
电催化
·
理论计算
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Bin Meng,Erping Cao,Liwei Jia,Yuhua Zheng,Yanbin Cui
A variety of Cu-Fe oxide supported on Na 2 CO 3 -modified activated carbon (CuFeNaAC-X) catalysts were prepared via the impregnation and calcination methods and their desulfurization performance was evaluated at low-temperature. By optimizing the loading content of Cu-Fe, the sulfur capacity of the CuFeNaAC-5 reached a maximum of 430.09 mg/g, surpassing most activated carbon (AC) catalysts. EPR testing revealed that the loading of Cu-Fe oxide can activate oxygen to form superoxide radicals ( O 2 - ·), thereby promoting the catalytic oxidation of H 2 S. XPS testing revealed that upon loading of Cu-Fe oxide, the formation of FeOOH can facilitate the catalytic oxidation of H 2 S to sulfur (S) through a chain reaction. Combining EPR and XPS analyses, Na 2 CO 3 modification modulates the content of O 2 - ·, directing the formation of S and then significantly improving the catalyst’s desulfurization efficiency. Furthermore, CO 2 -TPD testing revealed that Na 2 CO 3 modification promotes the ionization of H 2 S to HS - , thereby enhancing the catalyst’s desulfurization performance. Based on the distribution of sulfur species in used catalysts, and the results of characterizations, a possible desulfurization mechanism of CuFeNaAC-X has been proposed.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2018
·Vol. 44
·期 9
·10420-10425
·
IF 3.057
Yurun Feng,Xue Guo,Hongyu Gong,Yujun Zhang,Yu Liu,Xiao Lin,Junjie Mao
PDCs-SiCN(Fe) ceramics were successfully fabricated with different content of ferric acetylacetonate (FA) by polymer-derived method. The effects of FA on the phase composition, microstructure, resistivity, dielectric properties , magnetic properties and microwave absorption properties of PDCs-SiCN(Fe) ceramics in the range of 2–18 GHz were investigated. The samples presented amorphous structure with a few crystalline phases of α-Fe and free carbon in the gaps, which were expected to be good soft magnetic materials . The average real permittivity and imaginary permittivity of PDCs-SiCN(Fe) ceramics with 50 wt% FA was about 14.1 and 5.3 respectively. Furthermore, the PDCs-SiCN(Fe) ceramics with 50 wt% FA addition content showed the broad absorption bandwidth in the 5.1–8.4 GHz with RL ≤ −10 dB (> 90% absorption) at 4 mm.
研究领域:
材料科学
·
功能陶瓷
·
电磁特性
·
吸波材料
·
复合材料
✓ 已验证
DOI
高影响因子
DALTON TRANSACTIONS
·
2021
·Vol. 50
·期 33
·11604-11609
·
IF 4.39
Guojuan Hai,Jianfeng Huang,Liyun Cao,Koji Kajiyoshi,Long Wang,Liangliang Feng,Yijun Liu,Limin Pan
Designing cost-effective bifunctional catalysts with high-performance and durability is of great significance for renewable energy systems. Herein, typical Fe, Ni-codoped W18O49/NF was prepared via a simple solvothermal method. The incorporation of Fe ions enhanced the electronic interaction and enlarged the electrochemically active surface area. The increased W4+ leads to a high proportion of unsaturated WO bonds, thus enhancing the adsorption capacity of water. The valence configuration of nickel (Ni) sites in such dual-cation doping is well adjusted, realizing a high proportion of trivalent Ni ions (Ni3+). Due to the orbital interactions, the Fe3+/Ni3+ ions and OER reaction intermediates exhibit strong orbital overlap. The positions of the valence band and conduction band are well modulated. As a result, the Fe, Ni-codoped W18O49/NF shows improved electrocatalytic activity, and achieves a low decomposition voltage of 1.58 V at 10 mA cm−2 and retains long-time stability.
研究领域:
材料科学
·
可再生能源
✓ 已验证
DOI
高影响因子
Scientific Reports
·
2019
·Vol. 9
·期 1
·1-11
·
IF 4.011
Li Junchao,Li Xuhua,Han Jindong,Meng Fansheng,Jiang Jinyuan,Li Jiao,Xu Chunlian,Li Yun
Mesoporous bimetallic Fe/Co was prepared as a Fenton-like catalyst to degrade the tetracycline hydrochlorides (TC). The nanocasting strategy with KIT-6 as a hard template was carried out to synthesize the mesoporous bimetallic catalyst. The mesoporous bimetallic Fe/Co catalyst was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), nitrogen adsorption-desorption isotherms, and Brunauer-Emmett-Teller (BET) method. The results showed that the catalyst has significant nanofeatures; the surface area, pore size, and particle size were 113.8 m 2 g −1 , 4 nm, and 10 nm, respectively. In addition, the effects of the operating parameters, such as the iron-to-cobalt ratio, pH, H 2 O 2 , and initial TC concentrations on its catalytic performance were investigated. The best operating parameters were as follows: iron-to-cobalt ratio = 2:1 to 1:1, pH = 5–9, H 2 O 2 : 30 mmol, initial TC less than 30 mg/L. Furthermore, the mesoporous bimetallic Fe/Co showed a good performance for degrading TC, achieving a removal rate of 86% of TC after 3 h under the reaction conditions of H 2 O 2 = 30 mmol, mesoporous bimetallic Fe/Co = 0.6 g/L, TC = 30 mg/L, pH = 7.0, and temperature = 25.5 °C. The mesoporous bimetallic Fe/Co catalyst shows good stability and reusability. This work demonstrated that mesoporous bimetallic Fe/Co has excellent catalytic efficiency, smaller amounts of leached ions, and wider pH range, which enhance its potential applications.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
APPLIED CLAY SCIENCE
·
2022
·
IF 5.907
Qianqian Chang,Boqiang Gao,Hu Yang
In this work, a series of novel composite adsorbents (k-TAFe) was designed and fabricated through a one-step method, that is, the chelation crosslinking of tannic acid, kaolin particles and different contents of Fe(III). k-TAFe had a high efficiency in adsorption of various fluoroquinolones antibiotics (FQs) from water. The detailed performance of k-TAFe in FQs adsorption, including the influences of Fe(III) content, solution pH, inorganic and organic additives, adsorption time and FQs' concentration, has been investigated systematically using ofloxacin (OFL), one of popular FQs, as an example. The maximal OFL uptake of k-TAFe was 0.405 mmol/g at an initial pH of 6.0. On the basis of the analysis of the x-ray photoelectron and fourier transform-infrared spectra before and after adsorption, the comparison in the apparent performance of k-TAFe in adsorption of seven FQs with similar structures and their two sub-structural analogs, and theoretical calculation, multiple adsorption mechanisms, including chelating effect, hydrogen bonding, electrostatic attraction , and π-π electron–donor–acceptor interactions, were involved and discussed in detail. Among them, chelating effect due to Fe(III) played a key role in OFL adsorption, and the addition of kaolin particles synergistically enhanced Fe(III) fixed on the composite adsorbents, increased the Fe(III) contents, and caused an improved OFL uptake of k-TAFe. Because of the evident advantages of environmental-friendliness, high adsorption performance and low cost, k-TAFe as an efficient adsorbent has notable application potentials in removal of FQs from water.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
Advanced Membranes
·
2024
·
IF 0
Junqi Ning,Cailin Yang,Qiuyu Mei,Limingming Huang,Kai Han
ABSTRACT The practical use of solar-driven interfacial evaporation is hampered by high cost, low photothermal conversion efficiency, and poor stability. Herein, a one-dimensional Fe/C constructed photothermal membrane is rationally developed to replace precious metals via the combination of Fe plasmon resonance with carbon molecular thermal vibration. The membrane exhibits excellent light absorbance (95.72%) and water evaporation rate (2.60 kg·m -2 ·h -1 ) leading to photothermal conversion efficiency up to 95.65% under 1 sun illumination. Janus Fe/C membrane with superhydrophobic and hydrophilic structure is further prepared by polydimethylsiloxane (PDMS) coating to improve long-term stability. The evaporation rate can be maintained at over 90% after 80 h illumination for real seawater treatment with metal ion removal efficiency >99%. It also shows high evaporation performance and stability for organic solvents such as IPA, and NMP. Thus, the 1D Fe/C constructed Janus membrane is a promising candidate for energy-saving solar-driven interfacial solvent evaporation including seawater desalination, wastewater treatment, and organic solvent purification.
研究领域:
材料科学
·
能源工程
·
环境工程
✓ 已验证
DOI
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
·
2021
·Vol. 21
·期 12
·6126-6134
·
IF 0
Chi Lili,Zhang Yuetong,Hua Yusheng,Xu Qiqi,Lv Mingzhu,Wang Huan,Xie Jiani,Yang Shengtao,Yong Yuan
Nanomaterials with intrinsic enzyme-mimicking characteristics, refered to as nanozymes, have become a hot research topic owing to their unique advantages of comparative low cost, high stability and large-scale preparation. Among them, Single-atom nanozymes (SAzymes), as novel nanozymes
with abundant atomically dispersed active sites, have caused specific attention in the development of nanozymes for their remarkable catalytic activities, maximum atomic utilization and excellent selectivity, the homogeneous catalytic sites and clear catalytic mechanisms. Herein, a novel single-atom
nanozyme based on Fe(III)-doped polydiaminopyridine nanofusiforms (Fe-PDAP SAzyme) was successfully proposed via facile oxidation polymerization strategy. With well-defined coordination structure and abundant Fe-Nx active sites similar to natural metalloproteases, the Fe-PDAP SAzyme exhibits
superior peroxidase-like activity by efficiently decomposing H2O2 for hydroxyl radical (.OH) species formation. Based on their superior peroxidase-like activity, colorimetric biosensing of H2O2 and glucose in vitro was performed by using a
typical 3,3,5,5-tetramethylbenzidine through a multienzyme biocatalytic cascade platform, exhibiting the superior specificity and sensitivity. This work not only provides a novel promising SAzyme-based biosensor but also paves an avenue for evaluating enzyme activity and broadens the application
of other nanozyme-based biosensors in the fields of biomedical diagnosis.
研究领域:
生物化学
·
纳米医学
·
分析化学
✓ 已验证
DOI
PubMed
SCIENCE OF THE TOTAL ENVIRONMENT
·
2021
·
IF 7.963
Meng Xia,Zheng Shen,Minyan Gu,Wenbo Chen,Wenjie Dong,Yalei Zhang
Microalgae residue was efficiently converted into lactic acid with a high yield (33.9%) under mild reaction conditions (210 °C, 2 h) over a Fe-Sn-Beta catalyst. Under the action of homogeneous H 3 O + and distinct Lewis acid sites on the catalyst, the production of lactic acid from microalgae residue underwent three main reaction steps: hydrolysis, isomerization , and retro-aldol condensation. Results demonstrated that the lipid component had a strong inhibitory effect on the production of lactic acid due to the formation of aromatics, esters, and complex nitrogenous heterocyclic compounds , which covered or poisoned the Lewis acid sites of the catalyst. The protein component acted as a chemical buffer that enhanced the production of lactic acid by controlling the release of monosaccharides from the carbohydrate fraction of microalgae and maintaining the catalytic activity of the catalyst. Thus, microalgae residue demonstrated great promise for the production of value-added chemicals.
研究领域:
生物化学
·
催化化学
✓ 已验证
DOI
PubMed
高影响因子
CHEMOSPHERE
·
2018
·
IF 4.427
Xukai Li,Weirui Chen,Yiming Tang,Laisheng Li
Fe-MCM-48 catalyst with a three-dimensional cubic pore structure was directly synthesized via a hydrothermal method, and the mineralization efficiency of diclofenac (DCF) in the catalytic ozonation process (Fe-MCM-48/O 3 ) was assessed. X-ray diffraction (XRD), N 2 adsorption desorption, transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) characterizations revealed that Fe existed in the framework of MCM-48, and Fe-MCM-48 possessed a large surface area and a highly ordered cubic mesoporous structure, which could accelerate reactants and products diffusion. Regarding mineralization efficiency, the addition of Fe-MCM-48 significantly improved total organic carbon (TOC) removal, and approximately 49.9% TOC were removed through the Fe-MCM-48/O 3 process at 60 min, which was 2.0 times higher than that in single ozonation. Due to this catalyst's superior structure, Fe-MCM-48 showed the better catalytic activity compared with Fe-MCM-41 and Fe loaded MCM-48 (Fe/MCM-48, Fe existed on the surface of MCM-48). DCF removal in the Fe-MCM-48/O 3 process was primarily based on ozone direct oxidation. The improvement of mineralization efficiency was attributed to the function of generated hydroxyl radicals (•OH), which indicated that the presence of Fe-MCM-48 accelerated ozone decomposition . Moreover, the negatively charged surface of Fe-MCM-48 and the proper pH value of the DCF solution played an essential role in OH generation.
研究领域:
环境科学
·
催化材料
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）