PHYSICAL CHEMISTRY CHEMICAL PHYSICS
·
2018
·Vol. 20
·期 22
·15192-15202
·
IF 3.906
Jinggao Wu,Maowen Xu,Chun Tang,Guannan Li,Hong He,Chang Ming Li
F-Doping effects on polyaniline-derived carbon coated Li3V2(PO4)3 (Li3V2(PO4)3−xFx@C) as a cathode for high performance Li rechargeable batteries are systematically investigated with a combined experimental and DFT theoretical calculation approach. The results clearly indicate that the doping amount has a significant impact on the rate capability and long cycle life. The optimal material (Li3V2(PO4)2.88F0.12@C) delivers 123.16 mA h g−1@2C, which is close to the theoretical value (133 mA h g−1), while showing a greatly improved cycle stability. Rietveld refinements show that the F− doping does not obey Vegard's Law, which may be attributed to the generated lower valence of V ions. AC impedance spectroscopy shows that the F-doping can achieve faster interfacial charge transfer for higher reaction reversibility. DFT calculations confirm that the lower V2+ (t2g↑)3 does exist in Li3V2(PO4)2.88F0.12, and the mean nearest neighbor Li–O bond length also increases for faster electrochemical kinetics, and further reveal that there is a tendency for a transition from the insulator to the n-type semiconductor due to the F dopant. The combined experimental and calculated results suggest that F-doping indeed greatly facilitates the charge transfer rate of the Li+ insertion/de-insertion process for better reversibility and enhances the Li+ diffusion rate to access the reaction sites, thus resulting in high rate capacity and cycling stability. This work not only offers a facile and effective approach to synthesize high performance Li-ion battery material for very promising practical applications, but also discloses scientific insights on element coating and doping to guide the electrode material design for fast electrode kinetics in energy storage devices.
研究领域:
材料科学
·
电化学
·
理论计算
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DOI
PubMed
高影响因子
DALTON TRANSACTIONS
·
2014
·Vol. 44
·期 1
·237-246
·
IF 4.097
Ying Liu,Lining Sun,Jinliang Liu,Yu-Xin Peng,Xiaoqian Ge,Liyi Shi,Wei Huang
A novel mesoporous nanosphere functionalized with 3-(aminopropyl)triethoxysilane (APTES) and 2-(5-bromothiophen)imidazo[4,5-f][1,10]phenanthroline (5-Br-Tip) was synthesized (denoted as Tip-MSS). With the coordinating function of the 5-Br-Tip to lanthanide (Ln) ions, for the first time, LnL3(5-Br-Tip) complexes were linked to the mesoporous nanospheres. The derived materials, named Ln-Tip-MSS (Ln = Eu, Tb, Sm, Nd, Yb), were characterized by Fourier-transform infrared (FT-IR) spectroscopy, TEM, XRD (wide-angle and small-angle), N2 adsorption/desorption analysis, and fluorescence spectroscopy. Upon excitation in the ligand absorption, the Ln-Tip-MSS nanomaterials show characteristic visible (Eu, Tb, Sm) and NIR (Sm, Nd, Yb) luminescence (multicolor emission covered from 450 nm to 1400 nm spectral region). Of importance is that, with low cytotoxicity and good biocompatibility given by the methyl thiazolyl tetrazolium (MTT) assay, the Eu-Tip-MSS was successfully applied to cell imaging in vitro based on the Eu3+ luminescence (under 405 nm excitation).
研究领域:
纳米医学
·
生物成像
·
材料科学
·
分子探针
·
化学生物学
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DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2026
·
IF 9.2
Qingsong Liu,Yan Zhu,Wentao Li,Junci Wu,Yi Zhang,Shouchun Ma,Chuanli Qin
Modified graphitic carbon nitride (MCN) was synthesized via calcinating β-alanine introduced melamine supramolecular precursors and poly(3-methylthiophene-co-fluorene) (P(3MT-co-F)) with improved planarity was prepared by polymerization of 3-methylthiophene (3MT) and fluorene (F) monomers. P(3MT-co-F)/MCN heterojunction was constructed by electrostatic self-assembly and the optimal 3P(3MT 1 -co-F 1 )/MCN exhibits excellent H 2 production performance of 11108 μmol h −1 g −1 under visible light, 150 times higher than MCN. The enhancement is attributed to the following aspects: First, F monomer as a rigid unit can regulate the main-chain torsion of P(3MT-co-F), enhancing planarity and facilitating intramolecular charge transport within copolymer. Second, N⋯S interactions and π-π stacking interactions at heterojunction interface improve the charge transfer and separation. Third, the incorporation of P(3MT-co-F) with narrow band gap into MCN not only broadens visible light absorption range and enhances visible light response, but also forms a Z-scheme heterojunction with MCN, further enhancing the charge separation and retaining the electrons with strong reducibility.
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高影响因子
ACS Applied Energy Materials
·
2025
·
IF 5.5
Yu Hao,Dongfang Chen,Dongyi Pu,Song Hu,Pavese Doague Nguela,Pucheng Pei,Xiaoming Xu
The development of efficient and durable hydrogen evolution reaction (HER) electrocatalysts is critical for sustainable energy conversion. Although platinum (Pt) serves as a benchmark HER catalyst, its practical application is hindered by the high cost, limited durability, and susceptibility to CO poisoning. In this work, we report a heterojunction Pt-based catalyst, Pt@NCL-MXene, synthesized by LiF etching of MXene and subsequent NH3 calcination. This process introduces dual nitrogen (N) and fluorine (F) doping and yields a nitrogen-doped carbon layer (NCL) coating on Pt nanoparticles with an average size of only 3.4 nm. Compared with conventional Pt–C catalysts, Pt@NCL-MXene exhibits a larger specific surface area, enhanced electron transfer efficiency, and an optimized d-band center, thereby facilitating both H* adsorption and desorption. As a result, Pt@NCL-MXene achieves a significantly lower overpotential of 73 mV at a current density of 100 mA cm–2, alongside improved kinetics and stability under operational conditions. Furthermore, the 9 wt % F-rich MXene support effectively suppresses CO adsorption on Pt, reducing the CO uptake to 0.224 mmol g–1, which is purportedly lower than that of Pt–C (0.264 mmol g–1), thereby mitigating CO poisoning and prolonging the catalyst’s service life. These findings offer insights into the rational design of advanced CO-resistant Pt-based HER electrocatalysts.
研究领域:
材料科学
·
能源化学
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DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2022
·
IF 5.304
Honglin Qin,Yuan Tao,Ruiting Niu,Bingyan Han,Lizhen Qiao
In this work, magnetic flower-like and fluorine-doped nickel oxide composites Fe 3 O 4 @SiO 2 @F/NiO were prepared and applied for the magnetic solid-phase extraction (MSPE) of five imidazole fungicides. The obtained materials were characterized by scanning electron microscopy, X-ray diffraction, energy-dispersive X-ray photoelectron spectroscopy and Brunauer-Emmett-Teller analysis to verify the successful synthesis. The effect of some experimental parameters on the extraction efficiency were explored to optimize the MSPE conditions, including the adsorbent dosage, ultrasonic time, salt concentration, sample solution pH, elution solvent type and volume. Then, method validation was performed under the optimal conditions in combination with high-performance liquid chromatography-ultraviolet detection. The determination coefficients ranged from 0.9956 to 0.9991, and the limits of detection and limits of quantification for the imidazole fungicides were 0.1–3 μg·L −1 and 0.3–10 μg·L −1 , respectively. Moreover, the intra-day and inter-day precisions were evaluated in three different concentrations with relative standard deviations in the range of 1.34 %-13.31 % and 4.96 %-13.92 %. At last, the proposed MSPE method was used to enrich and determine imidazole fungicides in tap water, milk and green tea samples, and the spiked recoveries were in the range of 77.93 %-119.38 %, demonstrating the potential of the method in the determination of imidazole fungicides from real samples.
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POLYMER
·
2020
·
IF 4.231
Yufei Liu,Siyuan Jiang,Wei Yan,Jun Qin,Min He,Shuhao Qin,Jie Yu
Improving complexation at the interfaces and regulating the crystal transformation behaviors of polyamide 6 (PA6) composites with high mechanical and thermal properties are essential for the industrial applications of PA6. In this work, the effects of adding p (N-(4-F-phenylmaleimide)-alt-styrene) (PFS) on the crystal transformation, thermostability, thermal conductivity , and mechanical properties of PA6 were investigated and discussed systematically. The resu---lts from heat deflection temperature (HDT), dynamic mechanical analysis (DMA ) and thermal conductivity tests indicate that PFS greatly increases the HDT, glass-transition temperature ( T g ), and thermal conductivity of PA6. Simultaneously, when the content of PFS is 10%, the tensile strength and flexural moduli of PA6/PFS composites are increased by 10.5 and 17.8% compared with that of pure PA6, respectively. The results from differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) show that PFS induces the transformation of PA6 from γ to α crystals by interfacial complexation. This work offers a facile approach for producing materials with high thermal and mechanical performances that can be potentially used in automobiles, electronics, and related technologies.
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Small
·
2023
·Vol. 19
·期 38
·2302055
·
IF 13.3
Chaojie Lyu,Yanle Li,Jiarun Cheng,Yuquan Yang,Kaili Wu,Jiwen Wu,Huichao Wang,Woon-Ming Lau,Ziqi Tian,Ning Wang,Jinlong Zheng
Heteroatoms Fe, F co-doped NiO hollow spheres (Fe, F-NiO) are designed, which simultaneously integrate promoted thermodynamics by electronic structure modulation with boosted reaction kinetics by nano-architectonics. Benefiting from the electronic structure co-regulation of Ni sites by introducing Fe and F atoms in NiO , as the rate-determined step (RDS), the Gibbs free energy of OH* intermediates (Δ G OH* ) for Fe, F-NiO catalyst is significantly decreased to 1.87 eV for oxygen evolution reaction (OER) compared with pristine NiO (2.23 eV), which reduces the energy barrier and improves the reaction activity. Besides, densities of states (DOS) result verifies the bandgap of Fe, F-NiO(100) is significantly decreased compared with pristine NiO(100), which is beneficial to promote electrons transfer efficiency in electrochemical system. Profiting by the synergistic effect, the Fe, F-NiO hollow spheres only require the overpotential of 215 mV for OER at 10 mA cm −2 and extraordinary durability under alkaline condition. The assembled Fe, F-NiO || Fe-Ni 2 P system only needs 1.51 V to reach 10 mA cm −2 , also exhibits outstanding electrocatalytic durability for continuous operation. More importantly, replacing the sluggish OER by advanced sulfion oxidation reaction (SOR) not only can realize the energy saving H 2 production and toxic substances degradation, but also bring additional economic benefits.
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PubMed
高影响因子
TALANTA
·
2023
·
IF 6.1
Jingyu Li,Miao Liu,Jiaxuan Li,Xianhua Liu
The establishment of simple and sensitive detection methods for fluoride ion (F − ) is of great importance for its effective prevention and control, and metal-organic framework (MOF) has attracted much attention for sensing applications due to its high surface areas and tunable structures. Herein, we successfully synthesized a fluorescent probe for ratiometric sensing of F − by encapsulating sensitized Tb 3+ in a MOF-on-MOF material (UIO66/MOF801, with the formula of C 48 H 28 O 32 Zr 6 and C 24 H 2 O 32 Zr 6 , respectively). We found that Tb 3+ @UIO66/MOF801 can be used as a built-in fluorescent probe for fluorescence-enhanced sensing of F − . Interestingly, the two fluorescence emission peaks of Tb 3+ @UIO66/MOF801 at 375 nm and 544 nm exhibit different fluorescence responses to F − under excitation at 300 nm. The 544 nm peak is sensitive to F − , while the 375 nm peak is insensitive to it. Photophysical analysis indicated that the photosensitive substance was formed, which promotes the absorption of 300 nm excitation light by the system. Self-calibrating fluorescent detection of F − was achieved due to the unequal energy transfer toward the two different emission centers. The detection limit of Tb 3+ @UIO66/MOF801 for F − was 4.029 μM, which is far lower than the WHO guideline for drinking water . Moreover, the ratiometric fluorescence strategy showed a high concentration tolerance of interference, because of its inner-reference effect. This work highlights the high potential of lanthanide ion encapsulated MOF-on-MOF as environmental sensors, and offers a scalable way for construction of the ratiometric fluorescence sensing systems.
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DOI
PubMed
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2019
·Vol. 43
·期 26
·10554-10559
·
IF 3.069
Xuelei Pang,Junqi Ge,Xudong Yu,Yajuan Li,Fengjuan Shen,Yanqiu Wang,Jujie Ren
A novel fluorescent organogelator (Y1) with both photoinduced electron transfer (PET) and intramolecular charge transfer (ICT) characteristics was designed and synthesized. The gelator Y1 could selectively recognize and discriminate fluoride and acetate ions in both solution and gel systems. Interestingly, addition of F− to the Y1 solution resulted in a dramatic enhancement of the fluorescence intensity and an obvious change in fluorescence color. However, the fluorescence intensity and color of the Y1 solution were strongly dependent on time after the addition of OAc−. Moreover, the organogel treated with F− experienced a quick gel-to-sol transition, while only color and fluorescence changes were observed without gel collapse after adding OAc− to the gel system. The sensing mechanisms were studied by 1H NMR, SEM and spectroscopic experiments.
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高影响因子
Journal of Cleaner Production
·
2024
·
IF 9.7
Min Wang,Guanghua Lu,Runren Jiang,Tianjian Dang,Yufang Chen,Jianchao Liu,Zhenhua Yan,Jun Hou
The widespread use of bisphenol F (BPF) as the commonly used alternative to bisphenol A (BPA) in the industry and its hazardous effects on ecological system and human health have attracted widespread attention. In this study, V C -FCN 0.3 hollow nanotube structure with confinement space effects and combined carbon vacancies was constructed by the spatial self-corrosion strategy, which effectively addressed the inherent limitations of conventional carbon nitride and achieved 100% removal rate of BPF within 2 h under visible light. Carbon vacancies not only accelerated the transfer of photogenerated carriers, but also enhanced the adsorption and activation of oxygen that accelerating the production of ·O 2 − , the main active species in this system. In addition, the special spatial structure shortened the mass transfer distance between the target pollutants and the active species. What's more, V C -FCN 0.3 showed excellent, stable, and eco-friendly photocatalytic degradation of bisphenol F over a wide pH range and in five water matrices, contributing effectively to the solution of purification of wastewater containing bisphenol analogues.
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Journal of Materials Chemistry C
·
2014
·Vol. 2
·期 28
·5651-5659
·
IF 0
Ling Fan,Ruili Cui,Xiuping Guo,Dong Qian,Beibei Qiu,Jun Yuan,Yongfang Li,Wenlong Huang,Junliang Yang,Weifang Liu,Xinjun Xu,Lidong Li,Yingping Zou
A new alkylthienyl substituted thieno[2,3-f]benzofuran (TBF)-based polymer (PTBFTDTBT) was synthesized and characterized. PTBFTDTBT had a high molecular weight, good solubility in common organic solvents, broad visible absorption from 300 to 750 nm, and a relatively deep highest occupied molecular orbital level (−5.2 eV). PTBFTDTBT also showed a field hole mobility up to the order of 10−2 using an organic field effect transistor (OFET) method and an order of 10−2 using a space-charge-limited current (SCLC) method. With the structure of indium tin oxide (ITO)/poly(3,4-ethylenedioxythiophene):polystyrene sulfonate/PTBFTDTBT:PC71BM (1 : 2, w/w)/Ca/Al, a power conversion efficiency of 6.42% was obtained with a high short circuit current (Jsc) of 13.51 mA cm−2 and fill factor (FF) of 61%, under the illumination of AM1.5G, at 100 mW cm−2, without any post-treatment. The study demonstrates that TBF is a promising building block for organic electronics.
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Nature Communications
·
2024
·Vol. 15
·期 1
·1-12
·
IF 14.7
Ye Pengcheng,Fang Keqing,Wang Haiyan,Wang Yahao,Huang Hao,Mo Chenbin,Ning Jiqiang,Hu Yong
Oxygen evolution reaction (OER) is critical to renewable energy conversion technologies, but the structure-activity relationships and underlying catalytic mechanisms in catalysts are not fully understood. We herein demonstrate a strategy to promote OER with simultaneously achieved lattice oxygen activation and enhanced local electric field by dual doping of cations and anions. Rough arrays of Fe and F co-doped CoO nanoneedles are constructed, and a low overpotential of 277 mV at 500 mA cm −2 is achieved. The dually doped Fe and F could cooperatively tailor the electronic properties of CoO, leading to improved metal-oxygen covalency and stimulated lattice oxygen activation. Particularly, Fe doping induces a synergetic effect of tip enhancement and proximity effect, which effectively concentrates OH − ions, optimizes reaction energy barrier and promotes O 2 desorption. This work demonstrates a conceptual strategy to couple lattice oxygen and local electric field for effective electrocatalytic water oxidation.
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高影响因子
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