MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Qingbin Xu,Linchun Shi,Weijun Kong,Jing Wang,Peigen Xiao,Jinxin Liu
A meticulously engineered bacillus-shaped CoNi ZIF-MXene@MWCNT carbon cloth (CC) composite was synthesized through a one-step immersion method, which was employed in the development of a novel electrochemical (EC) sensor for the sensitive detection of salidroside (SAL) in Rhodiola. Characterization of the CoNi ZIF-MXene@MWCNT CC was conducted using scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray spectroscopy (EDS), and EC methods. The bacillus-shaped composite showcased an exceptionally high rate of active site exposure, superior conductivity, and electrocatalytic efficiency, attributed to the synergistic effects of the constituent materials. The remarkable electrocatalytic capability facilitated the redox reaction of SAL, marked by a significant enhancement in the current signal. This led to a concentration-dependent response enabling the quantitative detection of SAL. The mechanism of the redox reaction might be the oxidation of the phenolic hydroxyl group of SAL. Demonstrating high sensitivity, selectivity, and stability, this novel bacillus-shaped composite-based EC sensor achieved a low detection limit (LOD) of 0.0958 µ g/mL for SAL, within an effective linear range of 0.5–500 µg/mL. Importantly, the EC sensor proved to be adept at practical detection of SAL in Rhodiola samples with complex matrices, and the salidroside content of Rhodiola crenulata was much higher than that of Rhodiola rosea , indicating that Rhodiola crenulata may have a higher medicinal value, offering a promising avenue for rapid and sensitive detection of SAL.
研究领域:
电化学
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材料科学
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分析化学
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药学
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DOI
高影响因子
Nano-Micro Letters
·
2021
·Vol. 13
·期 1
·1-20
·
IF 16.419
Cao Junming,Li Junzhi,Li Dongdong,Yuan Zeyu,Zhang Yuming,Shulga Valerii,Sun Ziqi,Han Wei
Combining with the advantages of two-dimensional (2D) nanomaterials, MXenes have shown great potential in next generation rechargeable batteries. Similar with other 2D materials, MXenes generally suffer severe self-agglomeration, low capacity, and unsatisfied durability, particularly for larger sodium/potassium ions, compromising their practical values. In this work, a novel ternary heterostructure self-assembled from transition metal selenides (MSe, M = Cu, Ni, and Co), MXene nanosheets and N-rich carbonaceous nanoribbons (CNRibs) with ultrafast ion transport properties is designed for sluggish sodium-ion (SIB) and potassium-ion (PIB) batteries. Benefiting from the diverse chemical characteristics, the positively charged MSe anchored onto the electronegative hydroxy (–OH) functionalized MXene surfaces through electrostatic adsorption, while the fungal-derived CNRibs bonded with the other side of MXene through amino bridging and hydrogen bonds. This unique MXene-based heterostructure prevents the restacking of 2D materials, increases the intrinsic conductivity, and most importantly, provides ultrafast interfacial ion transport pathways and extra surficial and interfacial storage sites, and thus, boosts the high-rate storage performances in SIB and PIB applications. Both the quantitatively kinetic analysis and the density functional theory (DFT) calculations revealed that the interfacial ion transport is several orders higher than that of the pristine MXenes, which delivered much enhanced Na + (536.3 mAh g −1 @ 0.1 A g −1 ) and K + (305.6 mAh g −1 @ 1.0 A g −1 ) storage capabilities and excellent long-term cycling stability. Therefore, this work provides new insights into 2D materials engineering and low-cost, but kinetically sluggish post-Li batteries.
研究领域:
材料科学
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电化学
·
能源存储
✓ 已验证
DOI
高影响因子
Materials Science and Engineering B-Advanced Functional Solid-State Materials
·
2025
·
IF 4.6
Zhenchao Gu,Yuanyuan Chen,Jiayi Li,Meng Chai,Lianke Zhang
As an electrode material for supercapacitors, MXene exhibits a natural tendency to stack during electrochemical processes, resulting in a significant degradation of capacitance performance. This study introduced Cu 2 O between MXene nanosheets to enhance the electrochemical performance of the material. Different morphologies of Cu 2 O/MXene films were fabricated through electrostatic self-assembly. Characterization revealed that larger Cu 2 O particles adhered to the edges of MXene nanosheets, while smaller nanoparticles were located between the MXene nanosheet layers. At a current density of 1 A g −1 , the mass specific capacitance of MXene was 240 F g −1 , the porous spherical Cu 2 O/MXene was 316 F g −1 , its specific capacitance reached 509 F g −1 at 0.5 A g −1 , and it maintained a capacitance retention of 69.3 % after 10,000 cycles. The results suggest that the superior electrochemical performance of the composite material can be attributed to the Cu 2 O dispersed on MXene, which provides additional pseudo-capacitance and increases the active sites.
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产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Shuyi Shen,Tao Ke,Dike Fang,Daohui Lin
Visible-light-driven photocatalysts with synergistic persulfate (PS) activation and photocatalysis possess enormous pollution-control potential. Herein, nitrogen and sulphur co-doped TiO 2 @C hybrid (N/S-TiO 2 @C) featuring the complementary visible-light photocatalysis and synergetic PS activation was synthesized by in situ oxidation of Ti 3 C 2 MXene and thereafter co-doping with N and S. Both anatase and rutile phases of TiO 2 were attained in N/S-TiO 2 @C. The decrease of TiO 2 bandgap (about 1.81 eV) and the defect of carbon layer caused by the N and S co-doping in both TiO 2 crystal and carbon layer enabled the synergistic enhancement of PS activation and photocatalysis. Complete degradation and 93.4% mineralization of sulfamethoxazole (SMZ, 10 mg/L) were achieved by dosing PS (2 mM) and N/S-TiO 2 @C (0.4 g/L) under visible light within 30 min. The degradation rate by N/S-TiO 2 @C through PS activation under visible light was 27.9-, 11.1-, and 2.30-fold higher than that by PS, N-TiO 2 @C, and S-TiO 2 @C alone, respectively. Reactive species SO 4 − , 1 O 2 , OH, and O 2 − , especially the former two, were determined dominating the SMZ degradation, and the degradation pathways were illustrated through intermediates identification. Moreover, N/S-TiO 2 @C kept excellent performance in activating PS to degrade SMZ in real water samples. These results indicate that N/S-TiO 2 @C is a stable and promising PS activator under visible light and has a good application potential in organic wastewater treatment.
研究领域:
环境科学
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材料科学
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化学工程
✓ 已验证
DOI
高影响因子
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING
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2020
·
IF 6.444
Xinxin Sheng,Dexuan Dong,Xiang Lu,Li Zhang,Ying Chen
Phase change materials (PCMs) have attracted great interest from researchers and have been widely developed in the field of solar thermal energy storage. Herein, a novel bio-based pomelo peel foam (PPF)/polyethylene glycol (PEG) composite PCM was designed and prepared via the simple impregnation process, which is further modified with low loading of MXene nanosheets for the purpose of improving its light-to-thermal conversion efficiency, thermal energy storage capability and thermal conductivity . With the incorporation of MXene nanosheets into PPF, the light-to-thermal conversion efficiency was improved obviously, the loading of PEG in form-stable composites phase change materials (FCPCMs) increased from 86.9 wt% (FCPCM-1) to 96.2 wt% (FCPCM-2, FCPCM-3 and FCPCM-4), and the thermal conductivity of obtained PPF@MXene/PEG FCPCMs was also improved (from 0.25 W/mK to 0.42 W/mK). It shows that the obtained PPF@MXene/PEG FCPCMs can be fully utilized in the field of solar thermal energy storage.
研究领域:
材料科学
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可再生能源
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太阳能储能
✓ 已验证
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
·
IF 9.965
Hankun Tan,Li Sun,Feng Xie,Jingjing Hu,Yaru Qu,Yihe Zhang
An alkali-treated MXene-SnS hybrid was prepared through hydrothermal methods. The Alk-MXene microplates provide highway for electronic transport, and the 3D wrinkled morphology ensures sufficient channels for Li + diffusion. The alkali treatment of MXene gives Alk-MXene@SnS enhanced binding strength, which allows the SnS nanosheets to remain firm binding with the Alk-MXene substrate during cycling and overcome capacity decay caused by large volume change. The synergy between the two components guarantees the hybrid excellent electrochemical properties by enabling high electronic/ionic conductivity and superior kinetic properties as evidenced by EIS, GITT tests and DFT calculation. As a result, the Alk-MXene@SnS retains specific capacities of 519 mAh/g after 100 cycles at 200 mA g −1 , and 330 mAh/g at the high rate of 8000 mA g −1 . In addition, a reversible capacity of 421 mAh/g can be provided after long term cycle test at 1000 mA g −1 for 800 cycles.
研究领域:
材料科学
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电化学
·
能源存储
✓ 已验证
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Muchen Lu,Jie Sun,Boyang Cui,Jian Zhang,Junlian Ren,Ruoyi Li
In this study, Pd/Ru/MXene/ nickel foam (NF) electrodes were prepared by the impregnation method and galvanostatic electrodeposition technique to investigate their electrocatalytic degradation of tetracycline (TC). Subsequently, the electron transfer mechanism during this degradation process was studied. Under the optimal conditions, the degradation efficiency of the Pd/Ru/MXene/NF composite electrode for TC reached 92.02 % at 60 min. Bursting experiments as well as H 2 O 2 generation experiments showed that OH, H* and ClO − together realized the degradation of TC. The composite electrode could effectively reduce the biotoxicity of the intermediate products of the TC degradation process. In order to reduce the aggregation of Pd and Ru nanoparticles, a scaffold structure and the introduction of a MXene intermediate layer were used to solve the problem. Electrocatalytic degradation of antibiotic molecules was facilitated by tuning the interface of the catalytic electrode to expose active sites and modulating the electronic state of the catalyst to enhance intrinsic activity.
研究领域:
环境科学
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材料科学
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电化学
✓ 已验证
DOI
高影响因子
FOOD CHEMISTRY
·
2022
·
IF 9.231
Haiyang Wang,Lin Cai,Yuwei Wang,Chang Liu,Guozhen Fang,Shuo Wang
A molecularly imprinted electrochemical sensor (MIES) modified with Cu-MOF and Ti 3 C 2 Tx was successfully prepared for the detection of hygromycin B in food. According to the pH sensitive property of reversible borate ester bonds, a molecularly imprinted polymers (MIP) were constructed on the modified gold electrode (GE) surface by electropolymerization to realize the controllable elution and adsorption of template molecules. Cu-MOF with large specific surface area and Ti 3 C 2 Tx with excellent electrical conductivity cooperate to improve the overall analytical performance of MIES. The morphology and electrochemical performance of the sensor were evaluated. Under the optimal experimental conditions, the method showed superior selectivity to hygromycin B with a linear range of 5 × 10 −9 –5 × 10 −6 M and a detection limit of 1.92 × 10 −9 M (S/N = 3). The detection results of this method are in good agreement with HPLC-MS/MS, which proves that the method has reliable practicability and accuracy.
研究领域:
食品科学
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分析化学
·
生物传感技术
✓ 已验证
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2021
·
IF 8.128
Qingying Feng,Yingqing Zhan,Wei Yang,Ao Sun,Hongyu Dong,Yu-Hsuan Chiao,Yucheng Liu,Ximin Chen,Yiwen Chen
Developing the multi-functional membranes including oil/water emulsion separation and removal of hazardous organic pollutants is essential to the purification of the complicated wastewater. However, it remains a daunting challenge to combine these intended functions while maintaining high separation efficiency. Herein, we developed a new 2D lamellar MXene/poly (arylene ether nitrile) (PEN) fibrous composite membrane through the self-assembly of TiO 2 nanoparticles intercalated MXene nanosheets onto the porous PEN nanofibrous mats and bioinspired polydopamine triggered chemical-crosslinking with polyethyleneimine (PEI). Such nano-intercalation and mussel-inspired crosslinking could effectively regulate the interlayer spacing of the MXene nanosheet skin layer and surface wettability of the composite membrane, which also further contributed to the fast separation and unique bifunctional feature. It was found that the MXene@TiO 2 /PEN fibrous composite membrane exhibited low oil-adhesion and superhydrophilic (WCA = 0°)/underwater superoleophobic (UOCA > 155°) properties, which could efficiently separate various surfactant-stabilized oil-in-water emulsions under low pressure of 0.04 MPa while keeping good stability (Under 1 M HCl and 2 M NaOH solutions) and recyclability. Interestingly, the fibrous composite membrane achieved favorable permeation flux of 908–1003 Lm −2 h −1 (2270–2507.5 Lm −2 h −1 bar −1 ) in comparison to other reported MXene based multifunctional composite membranes. Moreover, owing to the synergistic effect of MXene nanosheets and TiO 2 nanoparticles, the MXene@TiO 2 /PEN membrane showed excellent photocatalytic degradation performance for various dyes under visible light, i.e. the photocatalytic degradation efficiency for 15 ppm MB, MO, CV, and MeB solutions achieved 92.31%, 93.50%, 98.06%, and 99.30% within 60 min, respectively. Such 2D MXene bio-functional composite membranes with outstanding oil/water emulsions separation and photocatalytic degradation of dyes pave an avenue for treating complicated oily wastewater.
研究领域:
材料科学
·
环境科学
·
纳米技术
✓ 已验证
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Xingxing Li,Yanan Ma,Yang Yue,Guosheng Li,Chuankun Zhang,Minglei Cao,Yongchen Xiong,Jintao Zou,Yongheng Zhou,Yihua Gao
In recent years, the metal ion hybrid micro-supercapacitor (MSC) comprised of the battery-type Faradaic cathode based electrode and capacitor-type anode based electrode, can realize both high power and energy density, which becomes one of the most hottest areas of energy device. Herein, we demonstrated a zinc-ion hybrid micro-supercapacitor (ZIHMSC) by designing a Ti 3 C 2 T x MXene based electrode as capacitor-type anode and vanadium pentoxide (V 2 O 5 ) based electrode as battery-type cathode. In addition, the polyacrylamide (PAM) hydrogel where ZnSO 4 dissolved was chosen as the electrolyte, which effectively avoids the security risks, unlike other hybrid MSC based on the organic electrolytes. Meanwhile, the flexible ZIHMSC also exhibits well electrochemical properties, displaying a remarkable capacitance (129 mF cm −2 under 0.34 mA cm −2 ), high energy density (48.9 μWh cm −2 at 673 μW cm −2 ) and well-cycle stability (retaining ~ 77% capacitance after 10,000 cycles). This work supports a prospective routine for constructing the new-generation flexible micro-energy storage systems.
研究领域:
能量存储
·
材料科学
·
电化学
·
纳米技术
✓ 已验证
DOI
高影响因子
FUEL
·
2025
·
IF 7.5
Yongpeng Ma,Jianghui Du,Yifei Wu,Haobing Yan,Ruiqi Liu,Xiaojing Zhang,Hongzhong Zhang,Liming Zhou,Wenjun Huang
Among the diverse pollutants emitted from coal-fired and non-ferrous metal smelting flue gas, Hg 0 and CO have emerged as globally concerning environmental pollutants. However, the simultaneous abatement of multiple pollutants remains a critical challenge to be addressed. In this study, cobalt nanoclusters (Co NCs) were anchored on the terminal oxygen of Ti-O on Ti 3 C 2 MXene and formed asymmetric oxygen vacancies Co-Ov-Ti via a one-step hydrothermal method, yielding Co NCs/Ti 3 C 2 MXene with a morphology of hierarchical nanosheet-assembled spheres for Hg 0 and CO catalytic oxidation. Co NCs/Ti 3 C 2 MXene exhibited excellent 44 % and 52 % of Hg 0 and CO simultaneous removal efficiency at the optimal temperature of 250 °C, respectively. DFT calculations combined with energy barrier modeling were employed to investigate the reaction pathways and energy variations during the catalytic oxidation of Hg 0 and CO. Specifically, Hg 0 oxidation follows the Eley-Rideal mechanism, with a rate-determining energy barrier of 2.11 eV, while CO oxidation adheres to the Langmuir-Hinshelwood mechanism, featuring a rate-determining barrier of 0.17 eV. In the co-catalytic oxidation process, competitive adsorption between Hg 0 and CO was observed, primarily manifested as competition for Ov on the catalyst surface. This study provides a novel strategy for the synergistic control of multi-pollutants in industrial flue gas.
研究领域:
环境催化
·
材料科学
·
大气污染控制
·
物理化学
·
纳米材料
✓ 已验证
产品关联
DOI
高影响因子
Materials Science and Engineering B-Advanced Functional Solid-State Materials
·
2024
·
IF 3.9
Xianghui Feng,Chao Zeng,Fengxiang Sui,Jingya Liu,Kai Wu,Yonghong Cheng,Bing Xiao
Herein we demonstrate the synthesis of a new out-of-plane ordered double-transition-metal MAX phase known as Mo 2 VAlC 2 . Annealing the elemental powder mixture at 1540 °C with 2.0Mo: 1.0 V: 1.3Al: 1.8C results in a high yield of 91.2 wt% for Mo 2 VAlC 2 . The crystal structure of Mo 2 VAlC 2 is determined using Rietveld refinement of powder XRD, and which crystalizes into a hexagonal lattice structure with space group P6 3 /mmc. Employing the double spherical aberration corrected transmission electron microscopy, we confirm its chemically ordering behavior of one V layer sandwiched between two Mo layers. Additionally, its two-dimensional derivative Mo 2 VC 2 T x MXene has been successfully realized by etching the Al layer of Mo 2 VAlC 2 with hydrofluoric acid. The chemical composition and microstructure of Mo 2 VC 2 T x are inspected with SEM and EDX. The resulting multilayer and intercalated Mo 2 VC 2 T x exhibit the characteristic accordion-like and paper-like appearances, respectively. This work further expands the diversity of chemically ordered double-transition-metal MAX and MXene families.
研究领域:
材料科学
·
纳米技术
·
固体化学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）