文献检索

查找使用阿拉丁产品的科研文献

检索与阿拉丁产品相关的同行评审论文、DOI、PubMed 编号、期刊、作者、CAS 号及研究领域。

科研影响力快照

与阿拉丁产品相关的已发表科研成果

在搜索之前,这些指标可帮助访客快速了解产品关联科研的规模与质量。

346,438+ SCI 论文 与阿拉丁产品引用相关
2,295,919.25 总影响因子 匹配文献记录中影响因子的总和
81.20 最高期刊影响因子 匹配期刊中的最高 IF
6.63 平均期刊影响因子 匹配文献的平均 IF

参考指标 指标基于阿拉丁文献引用数据库及期刊影响因子记录。文献关联仅供科研参考,请以原始文献为准。

产品列表

视图 列表 网格

显示第337至348个,产品总数486个

设置提升方向
Ti3C2
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING · 2024 · IF 8.1

Polyaniline nanoparticles intercalated Ti3C2 MXene reinforced waterborne epoxy nanocomposites for electromagnetic wave absorption and anticorrosion coating applications

Qingsong Zhu,Xinyu Lei,Xiaoqin Zha,Eman Ramadan Elsharkawy,Chenye Ren,Huiyuan Chang,Salah M. El-Bahy,Juanna Ren,Renjie Wang,Zeinhom M. El-Bahy,Zhanhu Guo

Ti 3 C 2 MXene (TM) has great application potential in the field of wave absorption and corrosion resistance due to its unique performance, such as high specific surface area, high electrical conductivity, excellent mechanical and good chemical stability. However, it is difficult to obtain uniformly dispersed TM in the resin matrix due to rapid agglomeration behavior. It is difficult to obtain uniformly dispersed Ti 3 C 2 MXene (TM) in the resin matrix due to rapid agglomeration behavior. Herein, a novel method is presented to improve the corrosion protection and dispersion of TM by polymerizing polyaniline (PANI) nanoparticles between layers. The waterborne epoxy (WEP) coating with PANI-TM had high mechanical properties including impact resistance, adhesion, and flexibility and wear resistance. The PANI-TM-WEP composites can effectively absorb more than 90 % of the electromagnetic waves and demonstrate a decreased glass transition temperature of WEP from 128.0 to 107.6 ℃. Moreover, the |Z| 0.01Hz value of the PANI-TM 0.5 % was 1.2369 × 10 6 Ω·cm 2 , which was one order of magnitude larger than WEP coating. The high-performance anticorrosion of PANI intercalated TM coating is attributed to the synergistic effect of impermeable TM nanosheets and passivation effect of PANI. Therefore, PANI-TM is a potential choice for applications in the fields of anticorrosion and microwave absorption.

CAS / MDL: 62-53-3
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ENVIRONMENTAL RESEARCH · 2025 · IF 7.7

Efficient Degradation of Sulfadimethazine via a Novel Bimetallic MOF/Ti3C2 Cathode Using Reagent-Free Photoelectric Fenton Process

Huanran Chen,Jiahong He,Jibin An,Qiang Xu,Zhilin Xing

Sulfamethazine is an antibiotic whose anti-degradability and potential for water pollution have become a threat to water contamination. This study designed a composite cathode of Fe-MOF-525/Ti 3 C 2 to effectively remove SMT through Photoelectro-Fenton (PEF). Characterization and photoelectrochemical test results indicate that Fe-MOF-525/Ti 3 C 2 contains abundant active sites and exhibits excellent catalytic performance for the oxygen reduction reaction (ORR). Tests demonstrated that under optimized conditions, the PEF system achieved a removal rate of 95.6% for SMT and a cumulative H 2 O 2 concentration of 53 mM within 120 minutes. Reactive oxygen species (ROS) capture experiments confirmed that •OH and •O 2 − are the main ROS responsible for the degradation of SMT. Further studies investigated the possible degradation pathways. Overall, this work demonstrates an example of pollution control resulting from the philosophy of green chemistry, which offers a promising pathway to reduce the chemical demand for advanced oxidation processes.

✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
JOURNAL OF CATALYSIS · 2025 · IF 6.5

Beyond photocatalysis: “micro proton-battery-like” mechanism in V2O5/g-C3N4/Ti3C2 triads enables light-independent environmental remediation

Wenli Zhang,Xu Han,Xianhong Zheng,Yi Yang,Zhiqi Zhao,Haiwei Yang,Yi Zhang,Chengbo Du,Zongqian Wang,Qingbo Xu,Changlong Li,Peng Wang

Solar-driven photocatalysis is inherently limited by its diurnal discontinuity. Herein, we report a V 2 O 5 /g-C 3 N 4 /Ti 3 C 2 triadic composite that transcends this limitation via a “micro proton-battery-like” mechanism, enabling round-the-clock catalytic activity. The optimized composite achieves 93.9 % tetracycline degradation under visible light and, remarkably, maintains 64.1 % efficiency in the dark. This is underpinned by an 8-fold higher electron storage capacity (0.16 μmol/mg) than pristine g-C 3 N 4 , achieved via reversible V 5+ /V 4+ redox transitions. DFT calculations corroborate charge localization in V 3d orbitals during the light-driven “charging” phase and subsequent Ti 3 C 2 -mediated electron release for ·O 2 − generation in the dark. This work establishes a groundbreaking paradigm that unifies photocatalysis with electrochemical energy storage for persistent environmental remediation.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Enabling electron redistribution via electron-deficient boron quantum dots confined in Ti3C2 MXene for fast lithium-ion storage

Yuxuan Zhang,Junzhe Zhang,Hongming Zhao,Danfeng Zhang,Mei Wang,Peng Li,Liyong Wang,Yan-Bing He,Huiqi Wang

Quantum dots have been extensively utilized in diverse components of lithium-ion batteries (LIBs) due to their distinctive electronic structures, extremely high specific surface area, and remarkable interfacial regulation ability. In this work, a facile liquid-phase exfoliation method was employed to break down bulk boron into quantum-sized dots using a probe high-power ultrasonic crusher. The obtained boron quantum dots (BQDs) were confined within highly dispersed Ti 3 C 2 MXene, thereby forming BQDs/Ti 3 C 2 stacked composite anode materials for lithium-ion batteries. Based on the quantum confinement effect, BQDs exhibit superior electrochemical activity compared to bulk boron, providing abundant active sites for ion insertion and extraction. The well-dispersed BQDs in the Ti 3 C 2 MXene form a continuous network, facilitating efficient charge and ion diffusion and transport throughout the entire structure. Electron deficiency induced by BQDs occurs in the interlayers of Ti 3 C 2 MXene, thus the local electronic defect is introduced into the originally perfect periodic atomic arrangement and electronic potential field. This would cause ripples in the entire electronic system, leading to a redistribution of electrons. This not only enhances the charge transfer kinetics but also modulates the lithium-ion diffusion pathways through local electric field intensification. The as-prepared BQDs/Ti 3 C 2 stacked composite thus delivers an extremely high initial discharge capacity of 2514.5 mAh g −1 at 0.05 A g −1 , a large reversible capacity of 835.3 mAh g −1 at 0.1 A g −1 , and outstanding long-term cycle stability, with 958.0 mAh g −1 retained after 300 cycles. Notably, it also demonstrates exceptional long-term cycling performance at 2.0 A g −1 , with the capacity increasing from 459.5 mAh g −1 after 163 cycles to 1251.7 mAh g −1 after 759 cycles. The exploration of BQDs embedded in Ti 3 C 2 MXene is anticipated to inspire in-depth investigations into advanced BQD-powered MXene anode materials for LIBs.

研究领域: 材料科学 · 储能技术 · 纳米科技 · 电化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
PROGRESS IN ORGANIC COATINGS · 2025 · IF 7.3

Fabrication of waterborne antibacterial/antistatic nanocomposite coatings at low content of Ti3C2 nanosheets via quaternary ammonium salt modification

Wei Zhang,Lianfeng Wu,Shuxue Zhou

MXenes have attracted significant attention due to their unique properties, including antibacterial property and electrical conductivity. However, the antibacterial performance of MXenes-based coatings strongly depends on their superficial distribution. In this study, Ti 3 C 2 nanosheets were modified with dimethyloctadecyl [3-(trimethoxysilyl) propyl] ammonium (QAS) and further incorporated into waterborne epoxy coatings. Influence of modifier ratio on the distribution of QAS-modified Ti 3 C 2 nanosheets (Q-Ti 3 C 2 ) in coatings as well as on the antibacterial/antistatic performance of coatings was investigated. Appropriate amount of QAS (i.e., 10 %) for modification was critical to achieve high antibacterial performance at low content of Ti 3 C 2 nanosheets. The Q-Ti 3 C 2 embedded coating could get 99.4 % inhibition against E. coil and 100 % against S. aureus at 0.5 wt% loading. In contrast, the coating with unmodified Ti 3 C 2 only exhibited antibacterial rate of 85.3 % and 87.4 % for E. coil and S. aureus , respectively. The prominent antibacterial performance of Q-Ti 3 C 2 based coatings mainly results from the enriched residence of Ti 3 C 2 nanosheets at the upper layer of coatings and partially from the intrinsic antibacterial property of QAS. Additionally, the superficial distribution of Ti 3 C 2 nanosheets endowed the coatings with low surface resistance of 1.8 × 10 9  Ω, thereby conferring antistatic properties, and hence, facilitating antibacterial durability, even if the coating contains as low as 1 wt% Q-Ti 3 C 2 nanosheets. The nanocomposite coatings also exhibited better adhesion and high pencil hardness.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
SENSORS AND ACTUATORS B-CHEMICAL · 2021 · IF 7.46

A dual-mode aptasensor for foodborne pathogens detection using Pt, phenylboric acid and ferrocene modified Ti3C2 MXenes nanoprobe

Wenhai Wang,Shu Xiao,Zhijian Jia,Hongzhen Xie,Tianhua Li,Qiqin Wang,Ning Gan

Foodborne pathogens could result in serious health issues to public and thus some rapid analysis methods are urgent developed to monitor them. Herein, a dual-mode aptasensor based on electrochemical and colorimetric modes was constructed for the on-site detection of Vibrio parahaemolyticus ( V.P) in shrimps as a model. A novel nanoprobe ( [email protected] @MXenes) was developed to generate both electrochemical and colorimetric signals by modifying phenylboronic acid and ferrocene on Pt-MXenes nanocomposite . The nanoprobe exhibited both features of peroxidase mimic and specific recognition. Simultaneously, a V.P aptamer-functionalized electrode interface was fabricated to firstly specifically capture V.P, then conjugated with [email protected] @MXenes to form a sandwich complex. The complex could catalyze tetramethylbenzidine (TMB)-H 2 O 2 to produce a visible signal, and generate electrochemical signal simultaneously. Under the optimal condition, the aptasensor could determine as low as 5 CFU mL −1 V.P by electrochemical mode and 30 CFU mL −1 V.P by colorimetric mode. These superior performances may be attributed to that the synergistic catalysis and conductive effects deriving from Pt and MXenes on the nanoprobe can significantly amplify the signals to improve detection sensitivity. In particular, the dual detection system could mutually verify to achieve high accuracy. The aptasensor could also be expanded to rapid analysis of other food-borne pathogens through changing the aptamer on the electrode.

研究领域: 生物传感技术 · 食品安全检测
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
Advanced Materials Technologies · 2021 ·Vol. 6 ·期 6 ·2001157 · IF 7.848

3D Crinkled Alk-Ti3C2 MXene Based Flexible Piezoresistive Sensors with Ultra-High Sensitivity and Ultra-Wide Pressure Range

Yucui Xiang,Liang Fang,Fang Wu,Shufang Zhang,Haibo Ruan,Haijun Luo,Hong Zhang,Wanjun Li,Xingming Long,Baoshan Hu,Miao Zhou

The conflict between high sensitivity and wide sensing range greatly limits the extensive application of flexible pressure sensors. To produce a sensor with both high sensitivity and wide range is still a challenging work. Herein, flexible and highly sensitive piezoresistive sensors with wide sensing range are developed by combining the alkali-treated 3D crinkled MXene with microstructured polydimethylsiloxane (PDMS). Sensors with different-roughness PDMS films as flexible substrate and the unprocessed MXene as the conductive material are prepared to clarify the geometric design for the ultra-wide pressure range (0–800 kPa). Then, other sensors assembled by NaOH-alkalized 3D crinkled MXenes and rough PDMS are fabricated to illustrate that the material optimization can further enhance the sensitivity (up to 1104.38 kPa −1 ). The sensor shows a low limit of detection (17 Pa), fast response time (100 ms), good cycle stability (3000 cycles, 300 kPa), and can detect over a wide pressure range from that of the tiny pills, pulse, heartbeat, throat vibration, and the change of water weight, exhibiting a broad prospect in health monitoring systems and human-machine interaction.

研究领域: 材料科学 · 柔性电子学 · 传感器与执行器 · 纳米材料 · 可穿戴技术
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
ChemistrySelect · 2026 ·Vol. 11 ·期 20 ·e73535 · IF 2.3

A Concise Thermal Synthesis of Nitrogen Doped Mesoporous Carbon/Ti3C2 Nanocomposite Modified Electrode for Sensitive Detection of Isoquercetin

Wei Liu,Nannan Wang,Zhangyu Dai,Yanhua Sun,Qiongyao Zeng

This article is based on Zn-MOF-8 and uses a simple thermal synthesis method to prepare nitrogen-doped mesoporous carbon spheres (NMC), which is then combined with Ti 3 C 2 to prepare NMC/Ti 3 C 2 nanocomposites. It was characterized by SEM, EDS, XPS, FTIR, and electrochemical methods. The NMC/Ti 3 C 2 nanocomposite modified glassy carbon electrode (GCE) was used for sensitive detection of isoquercetin (IQ), achieving a wide linear range of 0.1–100 µM and a low detection limit of 0.073 µM (S/N = 3). The modified electrode also exhibits good selectivity, excellent anti-interference performance and can be used for actual sample detection. Graphical Nitrogen-doped mesoporous carbon spheres (NMC) were prepared using a simple thermal synthesis method with Zn-MOF-8 as a precursor. Subsequently, NMC was combined with Ti 3 C 2 to prepare NMC/Ti 3 C 2 nanocomposites. The NMC/Ti 3 C 2 nanocomposites were characterized using SEM, EDS, XPS, FTIR, and electrochemical methods. The NMC/Ti 3 C 2 nanocomposites were used to modify glass carbon electrodes (GCE), resulting in NMC/Ti 3 C 2 /GCE, which was employed for the sensitive detection of quercetin (IQ), achieving a wide linear range of 0.1–100 µM and a low detection limit of 0.073 µM (signal-to-noise ratio S/N = 3). The modified electrode also exhibited good selectivity and excellent anti-interference capability, making it suitable for detecting real samples.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
NANO · 2025 · IF 1.1

A Hollow Flower-Like Ti3C2@TiO2/G-C3N4 Z-Scheme Heterojunction for Effective Visible-Light-Driven Tetracycline Degradation

Jinglin Wang,Yuntian Wei,Shikun Chen,Chan Zheng

Efficient interfacial carrier transfer and separation can effectively enhance photocatalytic activity. In this study, a high-performance Z-scheme Ti 3 C 2 @TiO 2 /g-C 3 N 4 (TCTCN) ternary photocatalyst possessing a hollow flower-like architecture was synthesized using a reliable and effective method. Ti 3 C 2 @TiO 2 heterojunctions were constructed because exfoliated Ti 3 C 2 was partially oxidized to TiO 2 during the formation of hollow g-C 3 N 4 flower-like microspheres. In the Z-scheme heterojunction, the highly conductive metallic Ti 3 C 2 layers functioned as solid-state electron mediators, promoting electron–hole separation and migration efficiency. Under visible-light irradiation, the as-synthesized TCTCN photocatalyst possessed outstanding photocatalytic tetracycline (TC) degradation efficiency that was 2.03-fold and 1.25-fold higher than those of individual layered and hollow flower-like g-C 3 N 4 , respectively. The excellent photocatalytic TC degradation efficiency is attributed to the unique hollow structure and synergy among the Ti 3 C 2 , TiO 2 and g-C 3 N 4 structures in the TCTCN composite, enabling the Z-scheme-mechanism-assisted rapid separation and slow recombination of photoinduced electron–hole pairs because of the increased photocatalytic activity. Moreover, the TCTCN ternary hybrid photocatalysts possessed good physical stability and reusability, and the TC degradation efficiency negligibly decreased after five cycles. This work is an important development to establish a sound foundation for designing g-C 3 N 4 -based hybrid photocatalysts possessing substantial charge carrier separation and transfer for efficiently degrading antibiotics.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
Journal of Environmental Chemical Engineering · 2026 ·Vol. 14 ·期 5 ·124205 · IF 7.5

Ni-Ru bimetallic catalysts supported on Ti3C2 MXene-derived TiO2 for highly efficient low-temperature photothermal CO2 methanation

Kaige Chen,Jie Li,Yongxiang Wang,Yong Dai,Yongming Luo,Xiaohua Cao,Xiaoping Xing

Photothermal conversion of CO 2 to methane offers a promising pathway for simultaneous carbon recycling and renewable energy storage. To date, Ni-based catalysts dominate CO 2 methanation. However, their low-temperature activity under photothermal conditions still requires improvement. MTiO 2 derived from Ti 3 C 2 MXene retains its two-dimensional (2D) layered structure and excellent photothermal conversion properties. Herein, we synthesized Ru-Ni@MTiO 2 catalysts through hydrothermal treatment of Ni-impregnated MTiO 2 with controlled Ru loading ( x  = 1, 3 and 5 wt%). The optimal 3Ru-Ni@MTiO 2 catalyst achieved a CH 4 production rate of 86.25 mmol·g −1 ·h −1 at 300 °C, which is 1.3-fold higher than that of the Ru-free Ni@MTiO 2 counterpart. The superior catalytic performance stems from the synergistic electronic effect between Ni and Ru and their dual-site cooperation. Electron transfer from both Ru and MTiO 2 to Ni sites elevates the electron density of metallic Ni, which weakens the H-H bond and accelerates the dissociative adsorption of H 2 . Furthermore, Ru loading not only broadens the light absorption range and promotes photogenerated charge separation, but also increases the density of moderate basic sites, thus boosting CO 2 adsorption and activation. This work provides new insights into the design of bimetallic photothermal catalysts for CO 2 methanation.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF HAZARDOUS MATERIALS · 2026 · IF 10.6

Interface and defect engineering of hierarchical Ti3C2/Co@CeO2-NCNT nanocomposite for ultrasensitive electrochemical determination of pesticide bithionol

Zhifang Liu,Yuyi Song,Kunxiang Deng,Caiyu Ge,Xiang Ye,Xinyi Li,Yixi Xie,Pengcheng Zhao,Junjie Fei

Rational regulation of the interface and realization of synergistic electrocatalytic activity in functionalized structure represent a key strategy for developing high-selectivity electrochemical sensors toward emerging environmental pollutants. In this work, a hierarchical Ti 3 C 2 /Co@CeO 2 -NCNT composite electrode was rationally designed and fabricated via defect and interface engineering, and employed innovatively as a high-performance sensing platform for trace-level detection of bithionol (BT) in aquatic environments. In this architecture, the 2D conductive Ti 3 C 2 framework effectively disperses and stabilizes Co@CeO 2 -NCNT components, providing abundant pathways for efficient electron transfer. The as-obtained sensor delivers outstanding analytical performance, including a low limit of detection 2.82 nM, a wide linear range of 5 nM to 9 μM, and excellent stability and practicality in real water samples with satisfactory recoveries of 97.3% - 104.4%. Density functional theory (DFT) calculations confirm that p-d-f orbital hybridization greatly enhances BT adsorption, interfacial charge-transfer kinetics, and overall catalytic efficiency. This work not only provides a novel and sensitive electrochemical platform for BT detection, but also offers valuable guidance for the targeted design of advanced electrocatalytic materials for specific environmental pollutants by clarifying the synergistic mechanism of interface engineering and defect modulation.

✓ 已验证 DOI PubMed 高影响因子
查看原文 查看 PubMed
ANALYTICAL LETTERS · 2026 · IF 1.8

Selenized Ti3C2 MXene/MOF-Derived Porous Carbon Nanocomposite for the Simultaneous Electrochemical Determination of Acetaminophen and p-Aminophenol

Sumin Xu,Jiajia Zhang,Jianying Qu

Se@Ti3C2/CNs nanocomposites were successfully prepared through combining Ti3C2 MXene with ZIF-8-derived nitrogen-doped carbon materials (CNs) and employing a selenization strategy. The morphology and structural information of the material were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). Electrochemical investigation showed that this material exhibited outstanding electrocatalytic performance to acetaminophen (AP) and p-aminophenol (4-AP) and could detect them simultaneously in wider linear ranges of 0.10–400.00 μM and 0.10–330.00 μM respectively with detection limits of 45.7 and 46.0 nM, respectively. Analysis of water samples and artificial urine shows that the sensor based on this material provides satisfactory results for AP and 4-AP with satisfactory selectivity (current change is less than 5% of the initial value) and stability (current retains above 95% of its initial response after 10 days of storage), which offers potential applications in drug analysis and environmental monitoring.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
已复制

文献关联基于可获得的产品、CAS、DOI 及引用记录。收录不代表作者或出版方对阿拉丁产品的背书,请以原始文献为准。