ELECTROCHIMICA ACTA
·
2021
·
IF 6.901
Hui Zong,Ruijuan Qi,Ke Yu,Ziqiang Zhu
Hydrogen evolution is of great significance for reducing carbon emissions and realizing carbon-neutral. Hydrogen evolution reaction (HER) by water splitting has no carbon emissions and pollution, but it is still necessary to reduce cost and enhance catalytic activity. Herein, we report an ultra-thin Ti 2 NT x MXene-wrapped metal-organic frameworks (MOFs)-derived CoP composite (Ti 2 NT x @MOF-CoP), which is a bifunctional catalyst with low cost and high activity. We synthesize the Ti 2 NT x @MOF-CoP composite by phosphating the precursor ZIF-67 self-assembled with Ti 2 NT x MXene nanosheets. The Ti 2 NT x @MOF-CoP electrode shows competitive hydrogen evolution performance in a wide pH-range (current density of 10 mA cm −2 ) and has a low overpotential ( η ) of 112 mV in pH = 14 especially. The Ti 2 NT x @MOF-CoP electrode for OER also has a low η = 241 mV at 50 mA cm −2 . Based on the bifunctional activity of Ti 2 NT x @MOF-CoP in alkaline, we set a dual-electrode configuration for HER and OER. It has a bias of 1.61 V at 10 mA cm −2 , with impressive catalytic stability during a 20 h measurement. MOFs-derived CoP has a large specific surface area and strong catalytic activity. Ti 2 NT x as a novel member of the MXene family not only can increase the active sites, but also can improve the stability of heterojunction catalysts. It reveals that the Ti 2 NT x @MOF-CoP composite has great potential in hydrogen evolution and water oxidation, thus reducing carbon emissions and protecting the environment.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Chen Zhao,Zengyan Wei,Jie Zhang,Peigang He,Xiaoxiao Huang,Xiaoming Duan,Dechang Jia,Yu Zhou
Commercial graphite anodes show limited capacity in lithium-ion batteries, which inhibits the development of high-energy and high-power devices. Although the theoretical capacity of SnO 2 based anodes is three times higher than that of graphite, their practical application is hindered by the poor cycling stability. In this study, we report a ball-milling assisted exfoliation method for the scalable production of delaminated MXene nanosheets , followed by the preparation of 5 nm SnO 2 nanocrystals anchored on MXene nanosheets through a hydrothermal reaction . SnO 2 /MXenes nanocomposites exhibit long cycling life up to 1000 cycles with a high capacity of 904 mA h g −1 , which can be ascribed to the high conductivity of the MXene substrates, and the anchoring effect between SnO 2 nanoparticles and MXene sheets that can prevent crystal aggregation or collapse during cycling.
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高影响因子
DALTON TRANSACTIONS
·
2023
·Vol. 52
·期 44
·16413-16420
·
IF 4
Hankun Tan,Lei Zhang,Kaiyue Gao,Li Sun,Yihe Zhang,Feng Xie
2H phase MoS2 with a two-dimensional nanostructure, high chemical stability and large theoretical capacity has been considered as a potential anode material for lithium-ion batteries. However, some practical problems hinder the direct use of 2H-MoS2 for lithium storage, such as its volume expansion effect that leads to capacity loss and its semiconductor properties that cannot provide sufficient conductivity. Herein, the surface of an MXene with abundant surface groups was modified with CTAB to promote its ability to adsorb MoO42− anions, and then 2H-MoS2 with a few layers was directly grown on the surface of MXene sheets vertically. Thanks to the conductive MXene sheets and the vertically-supported high-capacity MoS2 on them, the as-obtained composite MXene@MoS2 offers enhanced performance in specific capacity, long cycling stability and high rate capability. A reversible specific capacity of 1198 mA h g−1 was retained after 100 cycles at 200 mA g−1 and a specific capacity of 717 mA h g−1 was exhibited at 8000 mA g−1.
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高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2020
·
IF 3.807
Quan Xu,Shuxian Chen,Jingkun Xu,Xuemin Duan,Limin Lu,Qingyun Tian,Xinxin Zhang,Yue Cai,Xinyu Lu,Liangmei Rao,Yongfang Yu
Luteolin (LUT) is one of the biologically active functional components, which was widely used in pharmacological applications. Thus, development of sensitive analytical methods for LUT determination is highly desired. In this work, Ti 3 C 2 -MXene/ZIF-67/CNTs heterostructure was exploited as a new electrochemical sensing platform for the sensitive determination of LUT. For the design of composite, the in-situ growth of ZIF-67 on CNTs surface ensures the stability of their binding and enhances the synergetic catalysis. Conductive MXene as matrix for the loading of ZIF-67/CNTs can promote the catalytic ability of composite. Electrochemical results show that the MXene/ZIF-67/CNTs modified electrode displays preeminent electrocatalytic activity and enhances electrochemical response to the redox reaction of LUT, ascribing to the synergistic effect of ZIF-67/CNTs and MXene. Upon the optimization of experimental parameters, e.g., pH, enrichment time, the sensor based on MXene/ZIF-67/CNTs composite exhibits excellent performance with wide linear relationship ranging from 0.1–1000 nM and a low limit of detection (LOD) of 0.03 nM (S/N = 3). Besides, MXene/ZIF-67/CNTs electrode performs high selectivity, stability, and acceptable reproducibility. Furthermore, the constructed sensor was successfully utilized to detect LUT in real samples with satisfactory recovery.
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高影响因子
JOURNAL OF ENVIRONMENTAL MANAGEMENT
·
2024
·
IF 8
Yuxuan Zhang,Jun Luo,Xiuyan Wang,Dunhan Zhang,Hongxia Xu,Yuanyuan Sun,Xueyuan Gu,Xin Hu,Bin Gao,Hongqiang Ren
MXenes, such as Ti 3 C 2 T x , demonstrate tremendous potential as heavy metal adsorbents due to their abundant reaction sites, high hydrophilicity , controllable interlayer spacing, and inherent reduction ability. However, their structural dependent pollutant removal performances and the related mechanisms are far less studied. Therefore, the removing abilities of Cr(VI) from water on Ti 3 C 2 T x MXenes with different structures (multilayer (ML-) and delaminated (DL-) Ti 3 C 2 T x ) synthesized via several etching techniques were evaluated. Focusing on the most effective ML- and DL-Ti 3 C 2 T x obtained by acid/fluoride salt etching, the impacts of structural variations on the Cr(VI) removal performances were explored. Both ML- and DL-Ti 3 C 2 T x demonstrate outstanding Cr(VI) adsorption and reduction capabilities, achieving equilibrium within 500 min with capacities of 92.7 and 205 mg/g, respectively. The differences in removal mechanisms stemed from the varying adsorption and reduction capacities of two MXenes. ML-Ti 3 C 2 T x , with lower surface area and porosity, had low adsorption capacity but superior reduction ability, efficiently converting most Cr(VI) to Cr(III) (66.8%). Conversely, DL-Ti 3 C 2 T x exhibited better removal efficiency but a lower capacity for reduction (45.7%). Notably, although the partial reduction of DL-Ti 3 C 2 T x to TiO 2 results in its limited chemical reduction capacity, Ti 3 C 2 T x might serve as a co-catalyst for TiO 2 , boosting the photoresponsiveness of DL-Ti 3 C 2 T x or TiO 2 through Ti 3 C 2 T x /TiO 2 heterojunctions , thereby facilitating photocatalysis to realize the reduction of Cr(VI). Both Ti 3 C 2 T x exhibited both excellent Cr(VI) removal capacity and detoxification capacity, demonstrating their high potential in treating heavy metal pollutants in wastewater.
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高影响因子
Small
·
2022
·Vol. 18
·期 30
·2202313
·
IF 15.153
Yuming Zhang,Jun-Ming Cao,Zeyu Yuan,Hao Xu,Dongdong Li,Yilin Li,Wei Han,Lili Wang
Magnesium-ion batteries (MIB) have gradually attracted attention owing to their high theoretical capacity, high safety, and low cost. A bimetallic metal–organic framework self-sacrificing template and a co-assembly strategy are used to prepare a high-performance, stable cycling NiSe 2 -CoSe 2 @TiVCT x (NCSe@TiVC) heterostructure MIB cathode that can be used as a flexible integrated unit to power future self-powered systems. Benefiting from the synergistic effect of TiVCT x MXene and NCSe, the NCSe@TiVC heterostructure electrode has a discharge-specific capacity of 136 mAh g −1 at 0.05 A g −1 and high cycling stability of over 500 cycles; the assembled pouch-cell device as flexible integrated unit exhibits good practicability. The magnesium ion storage mechanism is also validated using quantitative kinetic analysis, ex situ XRD, and XPS techniques. Density functional theory analysis indicates the most stable Mg-atom adsorption sites in the heterostructure. This study broadens the possibilities for applying the TiVCT x MXene heterostructure to energy storage materials and future self-powered flexible systems.
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高影响因子
ELECTROCHEMISTRY COMMUNICATIONS
·
2022
·
IF 5.443
Shuangshuang Zhao,Xuehang Wang,Narendra Kurra,Yury Gogotsi,Yu Gao
Two-dimensional (2D) niobium carbide, Nb 4 C 3 T x (T x : O, OH, and F), a representative member of the 43 MXene structural motif, has shown promising electrochemical performance in acidic electrolytes. The capacitive performance of Nb 4 C 3 T x in neutral aqueous electrolytes has been reported as moderate, but little effort has been made to improve it. In this paper, we report a method to introduce nanopores (pinholes) in Nb 4 C 3 T x MXene flakes by adjusting the etching time. The pinholes generated during the etching process improve ion diffusion pathways, which are otherwise hindered by the restacking of the 2D flakes. The “holey Nb 4 C 3 T x ” shows a 50 % improved rate capability at charge/discharge time scales of 1–2 s in 1 M Li 2 SO 4 , Na 2 SO 4 , and (NH 4 ) 2 SO 4 electrolytes. Our strategy of controlling the permeability of Nb 4 C 3 T x sheets can potentially be applied to other MXenes, providing guidance for improving the capacitance and rate capability of 2D materials.
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高影响因子
TALANTA
·
2025
·
IF 6.1
Jiamin Gong,Boran Zhang,Qinyi Li,Jiangli Shi,Xinling Liu,Yiping Wu,Ying Wen,Xiaoyu Guo,Haifeng Yang
Determination of antipsychotic drugs in humans is meaningful for both individualized therapy and therapeutic drug monitoring. Quetiapine (QTP), as one of the newly developed antipsychotic drugs, may pose risks to human health if used improperly. In this work, we synthesized a three-dimensional (3D) Au nanorods/MXene (Ti 3 C 2 T x )/nickel foams (named as AuNRs/MXene/NFs) composite material for detecting the antipsychotic drugs QTP. The prepared negatively charged MXene was first assembled on the surface of the NFs through electrostatic interaction to form MXene/NFs, and then the prepared AuNRs were anchored on the MXene/NFs to obtain the final 3D AuNRs/MXene/NFs. By integrating the porous structure and magnetic properties of NFs, large specific surface area of MXene, and the plasmonic hot spots of Au nanorods, the AuNRs/MXene/NFs-based SERS platform can easily and sensitively detect QTP in human urine with the limit of detection of 1.71 × 10 −9 mol/L. The linearity was distinguished over the concentration range of QTP from 1 × 10 −7 to 1 × 10 −4 mol/L (calculated at 1030 cm −1 ), with correlation coefficients (R 2 ) of 0.9955. The presented AuNRs/MXene/NFs-based SERS strategy realizes QTP detection using SERS technology and provides a novel protocol for the therapeutic drug monitoring.
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DOI
PubMed
高影响因子
JOURNAL OF CATALYSIS
·
2025
·
IF 6.5
Guangxu Yao,Jin Wan,Yangjun Luo,Dong Liu,Guolong Qiu,Huijuan Zhang,Yu Wang
Strategic localization of catalytically active sites within single-atom catalyst (SAC) architectures represents a pivotal determinant of material performance, particularly in two-dimensional (2D) substrates like MXenes, which offer intricate structural complexity and multifarious anchoring potentialities. Despite the burgeoning interest in non-metallic single-atom catalysts, a comprehensive understanding of site-specific loading mechanisms and their consequential catalytic implications remains substantially unexplored. Herein, we systematically investigate the precise incorporation of economically viable non-metallic elements—tellurium (Te) and arsenic (As)—onto Ti 3 C 2 MXene, a prototypical 2D material characterized by exceptional structural versatility. Our methodology delineates a nuanced approach to controllable single-atom immobilization, strategically differentiating between vacancy-embedded and surface-supported configurations. Through meticulous experimental design, we demonstrate that Te single atoms strategically integrated within titanium vacancies (C-TeSA-T) manifest superior Oxygen Reduction Reaction (ORR) electrocatalytic performance compared to surface-anchored counterparts (W-TeSA-T). Comprehensive characterization revealed remarkable electrocatalytic metrics, including a half-wave potential of 0.88 V vs. RHE and a limiting current density of 5.65 mA/cm 2 . Synergistic Density Functional Theory (DFT) computations and multi-potential X-ray Photoelectron Spectroscopic (XPS) analyses elucidated the intrinsic mechanistic landscape, conclusively identifying Te single atoms as primary catalytic centers and delineating the rate-determining reaction trajectory. This systematic investigation not only introduces an innovative paradigm for designing cost-effective non-metallic catalysts but also provides fundamental mechanistic insights into the intricate relationship between active site localization and catalytic performance, thereby advancing our fundamental understanding of site-specific catalysis in two-dimensional materials.
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高影响因子
CARBON
·
2024
·
IF 10.5
Junyu Lu,Lei Xu,Cheng Xie,Qun Wei,Qilin Jiang,Guangsheng Yao,Zhaohui Han
The rapid development of modern wireless communication technology makes electromagnetic wave pollution increasingly serious, necessitating the development of high-performance electromagnetic wave-absorbing materials. This study introduces a Ti 3 C 2 T x MXene hybrid carbon foam (HCF) that exhibits a tunable and efficient electromagnetic wave absorption performance. The HCF features a porous, multilayered structure, which enhances its multi-reflection properties, and a heterogeneous interface between the carbon foam and MXene boosting its dielectric loss. By regulating the content of MXene, the ratio of polarization loss to conduction loss can be regulated to achieve better impedance matching. As a result, the HCF demonstrated superb electromagnetic wave absorption performance with RL min = −72.25 dB and EAB max = 6.55 GHz. Furthermore, the minimum absorption frequency domain could be tuned within 8–14 GHz by varying the MXene content. The performance in radar wave absorption and electromagnetic-thermal conversion (ramp rate 85.81 °C/s from RT to 200 °C) proves that HCF is an efficient and reliable electromagnetic wave absorber, suitable for radar technology, microwave heating, and communication systems applications.
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DOI
高影响因子
MOLECULES
·
2025
·Vol. 30
·期 7
·1625
·
IF 4.6
Qing Tang,Qi Fan,Lei He,Ping Yu,Qing Huang,Yuanming Chen,Bingbing Fan,Kun Liang
MXene is widely used in the fields of microwave absorption and electromagnetic shielding to balance electromagnetic pollution with the development of communication technologies and human health, due to its excellent surface functional groups and tunable electronic properties. Although pure multilayered MXene has an excellent accordion-like structure, the weak dielectric loss and lack of magnetic loss result in poor microwave absorption performance. Here, we propose a strategy for the catalytic growth of CNTs by the electrophoretic deposition of adsorbed metal ions, leading to the successful preparation of Ni-MWCNTs/Ti3C2Txcomposites with a “layer-by-layer” structure, achieved through in situ regulated growth of CNTs. By introducing dielectric–magnetic synergy to improve the impedance matching conditions, and by regulating the diameter of the CNTs to alter the electromagnetic parameters of Ni-MWCNTs/Ti3C2Tx, the 2-Ni-MWCNTs/Ti3C2Txcomposite achieves the best reflection loss (RL) value of −44.08 dB and an effective absorption bandwidth of 1.52 GHz at only 2.49 mm thickness. This unique layered structure and the regulation strategy provide new opportunities for the development of few-layered MXene composites.
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PubMed
高影响因子
JOURNAL OF NANOBIOTECHNOLOGY
·
2025
·Vol. 23
·期 1
·1-22
·
IF 12.6
Yang Ningning,Hua Rongrong,Lai Yingying,Zhu Peijun,Ding Jian,Ma Xianhui,Yu Gaoxiang,Xia Yiheng,Liang Chao,Gao Weiyang,Wang Zhouguang,Zhang Hongyu,Yang Liangliang,Zhou Kailiang,Ge Lu
In the field of large-area trauma flap transplantation, preventing avascular necrosis remains a critical challenge. Key mechanisms for improving flap viability include angiogenesis promotion, oxidative stress inhibition, and cell death prevention. Recently, two-dimensional ultrathin Ti 3 C 2 T X (MXene) nanosheets have gained attention for their potential contributions to these processes, though MXene’s physiological impact on flap survival had not been previously investigated. This study is the first to confirm MXene's biological effects on the ischaemic microenvironment post-skin flap transplantation. Findings indicated that MXene significantly decreased the necrotic area in ischaemic flaps (37.96% ± 2.00%), with reductions of 30.40% ± 1.86% at 1 mg/mL and 20.19% ± 2.11% at 2 mg/mL in a concentration-dependent manner. Mechanistically, MXene facilitated in situ angiogenesis, mitigated oxidative stress, suppressed pro-inflammatory pyroptosis, and activated the PI3K-Akt pathway, particularly influencing vascular endothelial cells. Comparative transcriptome analysis of skin tissues with and without MXene treatment provided additional evidence, highlighting mechanisms such as pro-inflammatory pyroptosis, ROS metabolic processes, endothelial cell proliferation regulation, and PI3K-Akt signaling pathway activation. Overall, MXene demonstrated biological activity, effectively promoting ischaemic flaps survival and presenting a novel strategy for addressing ischaemic necrosis in skin flaps. Graphical abstract
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PubMed
高影响因子
危险品化学品经营许可证（带存储）