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Energy Storage Materials · 2022 · IF 20.831

Remove the –F Terminal Groups on Ti3C2Tx by Reaction with Sodium Metal to Enhance Pseudocapacitance

Xuewen Hu,Qicheng Zhang,Ning Gong,Xifan Chen,Lan Wang,Wenchao Peng,Yang Li,Fengbao Zhang,Xiaobin Fan

MXenes, a new family of two-dimensional materials, have been recognized as promising candidates for supercapacitors because of their unique chemical and physical properties. It has been proven that the terminal groups on MXenes play a decisive role in the pseudocapacitance . In this study, we report a highly efficient strategy to remove the –F terminal groups of Ti 3 C 2 T x . Our initial purpose was to explore the application of Ti 3 C 2 T x in sodium-ion batteries, whereas we found that almost all the –F terminal groups on Ti 3 C 2 T x could be eliminated by reaction with Na metal at high temperature, and abundant terminal –O was introduced after the subsequent washing step. The mechanism involved is clarified by combining systematical spectra analysis and density functional theory (DFT) calculations. In addition, the modulated Ti 3 C 2 T x MXene shows an extraordinarily high specific capacitance of 521 F·g −1 (at scan rate of 2 mV·s −1 ) or 578 F·g −1 (at a discharge rate of 1 A·g −1 ) in 1 м H 2 SO 4 , and 92% capacity could be retained even after 10000 cycles. This study should provide new insight into the surface chemistry of MXenes and facilitate its applications in a variety of fields.

CAS / MDL: 7664-39-3 7440-23-5
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COMPOSITES PART B-ENGINEERING · 2021 · IF 9.078

Ultrahigh-performance visible-light photodegradation enabled by direct Z-scheme AgI/(Na,F)–C3N4 composites

Saipeng Zhou,Mingming Hou,Yulong Sun,Wenzhe Zhao,Honglin Wang,Quanhui Guo,Xin Yu,Xinqi Ma,Junwei Zhao

Preparation of high-performance semiconductor photocatalysts is often considered to be the challenge and focus in dealing with water contaminations, and attracts numerous concerns and research interests nowadays. In this work, high-performance Z-scheme AgI/(Na,F) doped g-C 3 N 4 composites were synthesized by facile calcination and in-situ deposition methods and employed for ultrahigh-performance degradation of broad-spectrum antibiotics contaminants. The prepared (Na,F) doped g-C 3 N 4 showed narrower bandgaps, enhanced solar-light absorption, and highly improved visible-light photocatalytic performance. Besides, the strong combined interfaces between AgI nanoparticles and (Na,F) doped g-C 3 N 4 was contributing to visible-light harvesting and highly boosted charge separation of the samples, among which AgI/(Na,F)–CN-40% composite presented the best visible-light photocatalytic performance. The photocatalytic reaction rate constant of the AgI/(Na,F)–CN-40% composite was as high as approximately 0.2007 min −1 , which was 65.80 times of pristine g-C 3 N 4 and 3.60 times of AgI, mainly because of the construction of direct Z-scheme charge transfer pathways between AgI and (Na,F) doped g-C 3 N 4 . Finally, the radical scavenger experiments, possible degradation pathways , and photocatalytic mechanism were also proposed.

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CATALYSIS LETTERS · 2021 ·Vol. 152 ·期 5 ·1495-1505 · IF 3.186

Pd Nanoparticles on SBA-15 Containing F for 2-Ethyl-Anthraquinone Hydrogenation: Effects of Hydrophobicity

Zhang Yue,Wang Li,Ma Qingqing,Wang Nan,Pan Zhiyong

SBA-15 was modified via post-treatment with (NH 4 ) 2 SiF 6 and (NH 4 ) 3 AlF 6 solution (NSF-T and NAF-T) and applied as support of Pd catalysts for the hydrogenation of 2-ethyl-anthraquinone (EAQ). The characterization results revealed that F could be incorporated into the framework of SBA-15 by forming Si–F bond and the amount of F increased as the molar ratio of F in treating solution to Si species in SBA-15 (F/Si) increased from 0.1 to 0.4 for NSF-T and 0.3 to 0.6 for NAF-T. At the same F/Si, the incorporated amount of F was larger with NSF-T than with NAF-T, and the latter could simultaneously create acid sites in catalysts. The hydrophobicity of catalysts could be effectively improved by incorporating F into SBA-15 supports, which favored the catalytic performance. The catalyst on SBA-15 treated by NSF with F/Si of 0.3 exhibited the high initial activity (0.24 molH 2 ·gPd −1 ·min −1 ) and selectivity (95.5%). Graphic Abstract

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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING · 2021 · IF 3.927

Fabrication of F–Nb co-doped transparent conducting TiO2 films using the sol-gel method

Yang Ren,Haiyan He,Yunwei Wang,Ying Gong,Gaoyang Zhao

In this study, the F–Nb co-doped TiO 2 films (TFNO) were prepared on soda lime glass using the sol-gel method. Multielement doping was carried out to further improve the conductivity of Nb-doped TiO 2 (TNO) thin films by increasing the carrier concentration. The effect of fluorine doping on the microstructure, chemical composition, and optoelectronic properties of the TFNO films was investigated. The results show that the obtained films are polycrystalline with an anatase structure. Both niobium and fluorine are present in the TiO 2 films (as Nb 5+ and F − ). With increasing fluorine doping, the visible-light transmittance of the film increases slightly, and the carrier concentration continues to increase until saturation. However, the carrier mobility decreases gradually. The TFNO film exhibits the optimal optoelectronic properties, when the F:Ti atomic ratio is 0.5:1, reaching a resistivity of 0.02 Ω cm and a visible-light transmittance of 81%.

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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Boosting photocatalytic activity of C-F-TiO2 nanosheets derived from in-situ pyrolysis of MXene

Qi Zhao,Ye Yuan,Luyan Zhang,Liang Qiao,Cheng Ding,Kangshun Wang,Hongpeng Li,Jun Ma,Panpan Wang,Tianming Chen,Feihong Wang

Nonmetal doping is widely used in the modification of titanium dioxides (TiO 2 ) for photocatalytic applications. As a typical two-dimensional layered nanomaterial, the excellent physical and chemical properties of MXene materials have been the focus of current research. In this study, carbon and fluorine co-doped MXene derived TiO 2 nanosheets (labelled as C-F-TiO 2 ) were successfully synthesized and used as catalysts for degrading 2,4,6-trichlorophenol (2,4,6-TCP) under UV light irradiation. The C-F-TiO 2 with ultrathin nanosheet structure enhanced light absorption range and decreased the bandgaps. The degradation efficiency of 2,4,6-TCP by C-F-TiO 2 was over 99 % in 90 min, and the degradation rate was more than twice that of commercial TiO 2 . The degradation rate still remained about 90 % in 90 min after five cycles. The results of quenching experiments and electron spin resonance (ESR) illustrated that more reactive oxygen species (ROS) were generated in the C-F-TiO 2 /UV system, which was 1.5 times that of commercial pure TiO 2 , and • O 2 – was the dominant ROS for 2,4,6-TCP degradation. This study provided insight to utilize physicochemical characteristics of MXene to synthesize non-metal co-doped TiO 2 nanosheet as a catalyst, exhibiting excellent reactivity in the potential application for organic pollutant degradation.

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MATERIALS LETTERS · 2015 · IF 2.489

Multi-layer SiC/Mg and F co-substituted hydroxyapatite/chitosan bioactive coating for carbon fibers

Zhang Leilei,Li Hejun,Li Kezhi,Liu Shoujie,Zhang Yulei,Yao Pei,Zhang Wenqi,Chen Guanzheng

A multi-layer coating composed of SiC inner-layer and Mg and F co-substituted hydroxyapatite/chitosan hybrid out-layer for carbon fibers has been synthesized using a combination method of chemical vapor deposition , electrochemical deposition and ion exchange method. The morphology, microstructure and in-vitro bioactivity of the multi-layer coating are analyzed. The results show that the SiC inner-layer exhibits a squamous shape. Mg and F co-substituted hydroxyapatite/chitosan hybrid out-layer covers the SiC inner-layer coated carbon fiber entirely and uniformly with a flat structure. The multi-layer coating could induce the precipitation of particle-shaped apatite crystals with Ca/P molar ratios of 1.34–1.51 on its surface in simulated body fluid. The multi-layer SiC/Mg and F co-substituted hydroxyapatite/chitosan coated carbon fibers should have potential application for tissue engineering.

CAS / MDL: 9012-76-4
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Nanoscale · 2015 ·Vol. 7 ·期 47 ·20033-20041 · IF 7.394

Bio-nanoplatforms based on carbon dots conjugating with F-substituted nano-hydroxyapatite for cellular imaging

Yafei Zhao,Liyi Shi,Jianhui Fang,Xin Feng

Carbon dots (CDs) have shown great promise in a wide range of bioapplications due to their tunable optical properties and noncytotoxicity. For the first time, a rational strategy was designed to construct new bio-nanoplatforms based on carboxylic acid terminated CDs (CDs-COOH) conjugating with amino terminated F-substituted nano-hydroxyapatite (NFAp) via EDC/NHS coupling chemistry. The monodisperse NFAp nanorods were functionalized with o-phosphoethanolamine (PEA) to provide them with amino groups and render them hydrophilic with respect to the ligand exchange process. The CDs-COOH@PEA-NFAp conjugates exhibits bright blue fluorescence under UV illumination, excellent photostability and colloidal stability. Due to their low cytotoxicity and good biocompatibility as determined by methyl thiazolyl tetrazolium (MTT) assay, the CDs-COOH@PEA-NFAp conjugates were successfully applied as bio-nanoplatforms to MCF-7 breast cancer cells for cellular imaging in vitro. More importantly, the functional CDs conjugated to NFAp provide an extended and general approach to construct different water-soluble NFAp bio-nanoplatforms for other easily functionalised luminescent materials. Therefore, these green nanoplatforms may be a prospective candidate for applications in bioimaging or targeted biological therapy and drug delivery.

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MICROPOROUS AND MESOPOROUS MATERIALS · 2020 · IF 4.551

Green synthesis of low-silica CHA zeolite without organic structural directing agents, fluoride media and seeds

Xiaojun Deng,Ping Zhou,Xiayan Yan,Renjin Xiong,Huaqin Kou,Wenhua Luo

To spare the use of OSDA and fluorides, for the sake of reducing cost and environmental conservation, a green and efficient synthesis recipe of low-silica CHA zeolites has been demonstrated, without using seeds or any other zeolites. The main factors that determine the formation of CHA zeolites have been investgated systemmatically, and several rules are obtained. (i) just considering simple memallic cations acting as the SDA , K + is indispensable for the formation of CHA framework, with noting that K + can also direct to MER topology. (ii) working as catalyst or minerization agent, OH − and F − function almost identically, but when the concentration of F − has reached a really high level or even only F − was used, CHA framework can not form because the intermediate fluoride complexes are inclined to produce small melecules of fluoride salts with morderate solubility over to enter the zeolite framework. (iii) at conditions of this work, the second stirring after the RT aging should be adopted since the contrastive tests have showed the benifits of the second stirring in making fewer or smaller impurity grains. (iv) when the concentration of K + is too high in reactive gels, with the other same conditions, MER over CHA framework is preferentially to form. (v) it is reasonable to consider the as-synthesized K-CHA materials can be used to research the novel “trapdoor” effect later. The authors considered the discussions and conclusions would offer some beneficial references to the green synthesis of zeolites and further understanding of the mechanism of hydrothermal treatment .

研究领域: 材料科学 · 环境化学 · 无机化学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Lanthanide-doped Mn2+-based perovskite-like single crystals: Switching on highly thermal-stable near-infrared emission and LED device

Yue Su,Lifang Yuan,Bo Wang,Sijian Wu,Yahong Jin

Metal halide perovskites (MHPs) have sparked ongoing research interest due to their high-performance optoelectronic properties. However, blue-light excitable near-infrared (NIR) emitting MHPs is still inaccessible and the achievement of robust thermal-quenching resistance so far remains a huge challenge. In this work, we report on the synthesis of lead-free all-inorganic Mn 2+ -based perovskite-like single crystals using the designed nonstoichiometric precursor ratio. The special crystal structure endows Mn 2+ with efficient blue light excitation and red emission, which enables the capabilities of a good matching with commercial blue LED chips and an efficient sensitization for Ln 3+ emitters. The incorporations of Yb 3+ , Er 3+ , and Ho 3+ functionalize the CsMnCl 3 single crystals with multiple NIR emissions by virtue of feeding the energy from Mn 2+ to Ln 3+ via multi-channels. Most remarkable is the achievement of the robust thermal-quenching resistance, exhibiting (near-) zero-thermal-quenching and even anti-thermal quenching, of the Ln 3+ NIR emissions above room temperature . Finally, as a proof-of-concept study, a prototype of an NIR-LED device was fabricated. This work not only provides a general strategy to unlock the blue-light excitable NIR emission from f-f transitions of Ln 3+ ions, and a fundamental understanding of the sensitization-activation mechanisms in Ln 3+ -functionalized manganese (Ⅱ)-based perovskite-like phosphor, but also endows the MHPs with optical functionalities for the future high-potential applications, such as NIR phosphor-converted LEDs, and optical telecommunication.

研究领域: 材料科学 · 光电学 · 光子学 · 固体物理 · 无机化学
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FOOD CHEMISTRY · 2024 · IF 8.5

Fabrication of fluorinated magnetic microporous organic network for selective and efficient extraction of benzoylurea insecticides in tea beverages

Hui-Ping Yu,Qian-Qian Xu,Xin Wang,Yuan-Yuan Cui,He-Fang Wang,Cheng-Xiong Yang

In this work, a novel fluorinated magnetic microporous organic network (Fe 3 O 4 @FMON) was exquisitely designed and synthesized for highly efficient and selective magnetic solid phase extraction (MSPE) of fluorinated benzoylurea insecticides (BUs) from complex tea beverage samples. The Fe 3 O 4 @FMON exhibited good extraction for BUs via the pre-designed hydrophobic, π-π stacking, hydrogen bonding and specific F F interactions. A sensitive Fe 3 O 4 @FMON-based MSPE-HPLC-UV method with wide linear range (0.10–1000 μg L −1 , R 2  ≥ 0.996), low limits of detection (0.01–0.02 μg L −1 ), and large enrichment factors (85.6–98.0) for BUs from tea beverage samples was developed. By decorating F elements within MON's networks, the Fe 3 O 4 @FMON characterized good hydrophobicity and chemical stability, which could be reused at least 8 times without decrease of recoveries. This work demonstrated the great prospects of Fe 3 O 4 @FMON for enriching trace BUs from complex substrates and triggered the potential of FMON for sample pretreatment of fluorinated analytes.

研究领域: 分析化学 · 环境科学 · 材料科学 · 食品科学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2024 ·Vol. 35 ·期 27 ·1-9 · IF 2.8

A novel low-permittivity Lu2MgAl4SiO12 microwave dielectric ceramic with garnet-type structure

He Chuansheng,Li Yingxiang,Wang Fei,Hou Zegui,Liu Wei,Liang Deyin,Tang Bin,Fang Zixuan,Shi Zitao,Chen Jingjing,Li Hao

For the timely transmission of signals, the research of low dielectric constant microwave ceramics is essential. In this study, a new type of low-permittivity Lu 2 MgAl 4 SiO 12 microwave dielectric ceramic was prepared by traditional solid-phase method. The successful synthesis of Lu 2 MgAl 4 SiO 12 ceramics with cubic crystal system and space group Ia-3d (230) was determined by XRD and Rietveld refinement. SEM observation confirmed the garnet structure of Lu 2 MgAl 4 SiO 12 ceramics, and verified the dense structure of the ceramic samples with a relative density of 99.1%. In addition, the influence of relative density and packing fraction on Q  ×  f was studied by analyzing the Lu 2 MgAl 4 SiO 12 system. The findings revealed that τ f was affected by the valence state of V Si-O bond. Finally, Lu 2 MgAl 4 SiO 12 sample sintered at 1490 °C demonstrated notable microwave properties ( ε r  = 9.13, Q  ×  f  = 15,100 GHz, τ f  = –47.1 ppm/°C).

研究领域: 材料科学 · 无机非金属材料 · 介电材料 · 微波技术 · 陶瓷工程 · 晶体结构
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CERAMICS INTERNATIONAL · 2025 ·Vol. 51 ·期 30 ·63013-63021 · IF 5.6

Structural characteristics and microwave dielectric properties of low-loss spinel type Li2M2Ga2Ti3O12 (M = Mg, Zn) ceramics for dielectric resonant antenna applications

Ning Zhang,Junqi Chen,Ning Guan,Huaicheng Xiang,Ying Tang,Yuandong Qin,Liang Fang

Two novel ceramics, Li 2 Mg 2 Ga 2 Ti 3 O 12 (LMGT) and Li 2 Zn 2 Ga 2 Ti 3 O 12 (LZGT), featuring a spinel structure, were synthesized utilizing the solid-state method. Comprehensive characterization confirms that LZGT ( P 4 3 32) forms a B-site 1:3 ordered spinel, while LMGT ( Fd -3 m ) adopts a disordered spinel structure. The ceramics exhibit outstanding microwave dielectric properties, characterized by low ε r of 14.92 and 19.11, high Q×f of 120,000 and 93,800 GHz, and negative τ f of −40.21 and −32.83 ppm/°C for LMGT and LZGT, respectively. The observed ε r values significantly exceed theoretical values due to underestimated Ti 4+ polarizability along with the rattling effect of Ti 4+ and Ga 3+ . Q×f values correlate with packing fraction, lattice energy, and electrical properties. The negative τ f values stem from dominant positive τ ε and τ αm contributions. Utilizing LMGT with ultra-low loss, a dielectric resonator antenna was designed, achieving a radiation efficiency of 93.01 % and a gain of 6.12 dBi at 6.60 GHz, highlighting significant potential for C-band communication satellite applications.

研究领域: 材料科学 · 无机非金属材料 · 电子功能材料 · 微波技术 · 天线工程 · 固态化学
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