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Ti3C2-MXene
ACS Applied Materials & Interfaces · 2023 · IF 9.5

Magnetic Ti3C2 MXene Nanosheets Prepared for Enrichment of Phosphopeptides

Sen Zhang,Jia-yuan Li,Wei Gao,Jun-qin Qiao,Hong-zhen Lian

MXenes have received lots of attention since discovered and have been applied in various fields. In this work, Ti3C2–Fe3O4 composites with exposed non-modified Ti3C2 MXene nanosheets were designed and prepared by an in situ growth strategy and then applied in the enrichment of phosphopeptides. The two-dimensional composites could interact with the phosphopeptides through a metal oxide affinity chromatography mechanism provided by Ti–O and Fe–O bonds and a hydrophilic interaction chromatography mechanism by surface hydroxyl groups. This magnetic nanomaterial with a specific surface area of 66.1 m2·g–1 had high sensitivity to phosphopeptides (0.5 nmol·L–1) and high selectivity (1:1000 of the molar ratio of β-casein to bovine serum albumin). Non-fat milk was adopted as a real sample to preliminarily examine the applicability of the Ti3C2–Fe3O4-based protocol. Subsequently, Qingkailing injection, a kind of traditional Chinese medicine injection, was introduced to further explore the suitability of the nanocomposites for phosphopeptide enrichment from more complex matrices and satisfactory results were obtained.

研究领域: 材料科学 · 分析化学 · 生物技术
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RSC Advances · 2025 ·Vol. 15 ·期 14 ·11271-11282 · IF 4.6

A simple self-assembly aptasensor for ultrasensitive detection of kanamycin based on carbon dots and Ti3C2 MXene nanocomposite

Fang Li,Shuyue Xiong,Yijun Tan,Mingming Luo,Zijian Wu

Antibiotics play an excellent role in preventing and treating animal diseases, but their improper use poses a potential threat to public health. Designing a sensing platform to detect trace amounts of antibiotic residues in actual samples is a significant challenge. To achieve this objective, a self-assembly aptasensor based on a two-round signal amplification strategy for kanamycin (KANA) trace detection was demonstrated by employing carbon dot (CD) decorated Ti3C2 MXene as electrode modification material and the complex of double-stranded DNA (dsDNA) and methylene blue (MB) as probes, where dsDNA was composed of complementary DNA (cDNA) and aptamers. The CDs can effectively suppress the self-stacking of Ti3C2 MXene to promote electron transfer and provide plenty of exposed active sites for the aptamer to capture KANA precisely. The MB inserted into dsDNA would be liberated upon interaction with KANA due to a competitive process that occurs among cDNA and KANA, reducing electrical signal. Under the optimal conditions, the constructed aptasensor exhibited a good linear relationship between the output signal and the logarithm of KANA concentration in the range of 1 fM–1 mM, and the limit of detection is 0.892 fM. The satisfactory selectivity, stability, and reproducibility suggested that the prepared aptasensor can be a universal platform to detect other antibiotic residues by anchoring corresponding aptamers. Furthermore, it has been successfully applied to determine KANA in milk samples (recovery rates ranged from 101.01% to 107.21%, and the RSD was below 5%), demonstrating potential application prospects in the food-safety analysis field.

研究领域: 分析化学 · 食品安全 · 生物传感技术
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Ti3C2-MXene composite films functionalized with polypyrrole and ionic liquid-based microemulsion particles for supercapacitor applications

Qi Fan,Ruizheng Zhao,Mengjiao Yi,Ping Qi,Chunxiao Chai,Hao Ying,Jingcheng Hao

Stemming from its unique structure and properties, Ti 3 C 2 -MXenes have stood out from the crowd of electrode materials due to effectively ameliorating imperfections of common ones for excellent energy storage. However, a major stumbling block in the further development of MXene-based supercapacitors is the inherent low capacities caused by severe restacking of nanosheets. Herein, we develop a simple, effective and innovative strategy, namely, introducing both polymerized polypyrrole (PPy) particles and ionic liquid (ILs)-based microemulsion particles as “dual spacers”, to fabricate functionalized Ti 3 C 2 -MXene composite films for high-performance and wide-temperature application in supercapacitors. The PPy particles acting as one “spacer” circumvent restacking issues of MXene nanosheets, while contribute to desirable capacitance of the hybrid material. ILs-based microemulsions spontaneously adsorbing onto PPy-Ti 3 C 2 T x nanosheets are conceived to be one more liquid “spacer” for fast ion diffusion kinetics and absent electrolyte imbibition steps, which is rarely reported in previous research for MXene-based electrode materials. These features endow the composite films with excellent specific capacitance, rate capability and cycling stability between 4 °C and 50 °C. At room temperature, the symmetric supercapacitor device based on the composite films delivers a maximum gravimetric energy density of 31.2 Wh kg −1 (at 1030.4 W kg −1 ) and reserves 91% of the initial specific capacitance with a coulombic efficiency of 91% after 2000 cycles. All these impressive results substantiate that the composite films prepared by ingenious structure design showcase huge potentials in advanced MXene-based supercapacitors using various ionic liquid electrolytes.

CAS / MDL: 7789-24-4
研究领域: 材料科学 · 能源存储技术
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Nanoscale · 2019 ·Vol. 11 ·期 30 ·14123-14133 · IF 6.97

Highly fluorescent Ti3C2 MXene quantum dots for macrophage labeling and Cu2+ ion sensing

Qingwen Guan,Junfei Ma,Wenjing Yang,Rui Zhang,Xiaojie Zhang,Xiaoxiao Dong,Yuting Fan,Lulu Cai,Yi Cao,Yilin Zhang,Neng Li,Quan Xu

Quantum dots, derived from two-dimensional (2D) materials, have shown promise in bioimaging, sensing and photothermal applications, and in white light emitting devices (WLEDs). Herein, nitrogen and phosphorus functionalized Ti3C2 MXene based quantum dots (N,P-MQDs) were successfully prepared through a top-bottom hydrothermal method. This type of photoluminescent quantum dots has realized green fluorescence for the first time at around 560 nm with a photoluminescence quantum yield (PLQY) of 20.1%, the highest ever reported; meanwhile, it also exhibits excellent photostability and pH resistance capacities. Comprehensive characterization and well-resolved density functional theory (DFT) calculation were implemented to determine the mechanism of fluorescence shift and enhancement. Furthermore, the N,P-MQDs have been proved to efficiently act as fluorescent probes for macrophage labeling. In addition, the high sensitivity of the N,P-MQDs toward Cu2+ ions made them a low cost, sensitive, environment-friendly, and label-free fluorescence platform for Cu2+ detection. The outstanding performance of Ti3C2 MXene based quantum dots has demonstrated their great potential to be used as promising fluorescent probes in the fields of biological imaging, optical sensing, photoelectric conversion, etc.

研究领域: 生物成像 · 光学传感 · 材料科学 · 分析化学
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ACS Applied Materials & Interfaces · 2019 · IF 8.456

Boosting the Photocatalytic Ability of g-C3N4 for Hydrogen Production by Ti3C2 MXene Quantum Dots

Yujie Li,Lei Ding,Yichen Guo,Zhangqian Liang,Hongzhi Cui,Jian Tian

The big challenging issues in photocatalytic H2 evolution are efficient separation of the photoinduced carriers, the stability of the catalyst, enhancing quantum efficiency, and requiring photoinduced electrons to enrich on photocatalysts’ surface. Herein, Ti3C2 MXene quantum dots (QDs) possess the activity of Pt as a co-catalyst in promoting the photocatalytic H2 evolution to form heterostructures with g-C3N4 nanosheets (NSs) (denoted g-C3N4@Ti3C2 QDs). The photocatalytic H2 evolution rate of g-C3N4@Ti3C2 QD composites with an optimized Ti3C2 QD loading amounts (100 mL) is nearly 26, 3 and 10 times higher than pristine g-C3N4 NSs, Pt/g-C3N4, and Ti3C2 MXene sheet/g-C3N4, respectively. The Ti3C2 QDs increase the specific surface area of g-C3N4 and boost the density of the active site. Besides, metallic Ti3C2 QDs possess excellent electronic conductivity, causing the improvement of carrier transfer efficiency.

CAS / MDL: 9002-98-6
研究领域: 材料科学 · 能源化学
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MICROCHEMICAL JOURNAL · 2025 · IF 5.1

Alkalized Ti3C2 MXene-engineered cost-effective pencil graphite electrode to develop high-performance electrochemical sensor for simultaneous detection of Cd2+ and Pb2+

Lu Qian,Zuncai Gu,Mengting Liu,Tao Deng,Chenhao Zhang,Jing Qian,Xingyi Huang,Chengquan Wang

Heavy metals pose a significant threat to ecosystems and human health due to their toxicity and persistence. In this work, we developed a high-performance electrochemical sensor for simultaneous detection of Cd 2+ and Pb 2+ using a cost-effective pencil graphite electrode (PGE) modified with alkalized Ti 3 C 2 MXene (alk-MXene/PGE). Cyclic voltammetry and electrochemical impedance spectroscopy were utilized to examine the electrochemical characteristics of different PGEs. Studies revealed that the optimal PGE for subsequent application was the one with HB hardness and a diameter of 2 mm. Compared with bare PGE and Ti 3 C 2 MXene modified PGE, alk-MXene/PGE exhibited enhanced electrical conductivity and optimized electrochemical performance, enabling sensitive and simultaneous detection of Cd 2+ and Pb 2+ in a single run. Linear relationships were achieved for Cd 2+ in the range of 5.0 × 10 −4  ∼ 7.0 × 10 −2 mg/L and for Pb 2+ in the range of 2.0 × 10 −4  ∼ 8.0 × 10 −2 mg/L, with detection limits of 8.10 × 10 −6 mg/L and 9.12 × 10 −6 mg/L, respectively. The developed electrochemical sensor was successfully applied to scallop samples, demonstrating its good practicability. This study underscores the potential of alkalized Ti 3 C 2 MXene-modified PGEs in electrochemical sensing of Cd 2+ and Pb 2+ simultaneously, paving new avenues for food quality monitoring and environmental analysis.

CAS / MDL: 7789-24-4
研究领域: 环境科学 · 分析化学
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Nano Energy · 2021 · IF 17.881

2D amorphous-MoO3−x@Ti3C2-MXene non-van der Waals heterostructures as anode materials for lithium-ion batteries

Pengfei Yan,Liang Ji,Xiaopeng Liu,Qinghua Guan,Junling Guo,Yonglong Shen,Haijun Zhang,Weifeng Wei,Xinwei Cui,Qun Xu

2D heterostructures offer a great opportunity in seeking high-performing energy storage materials ; however, performance ceiling exists, limited by their van-der-Waals (vdW) interactions. Here, we explore a novel 2D, amorphous MoO 3−x (aMoO 3−x ) on Ti 3 C 2 -MXene, non-vdW heterostructure via a facile synthesis route. Density functional theory computations suggest that the non-vdW heterostructure can strongly stabilize aMoO 3−x while maintaining electrical conductivity at a high level. Facile 2D Li-ion diffusion can then be achieved in the restacked 2D non-vdW heterostructures due to the weakened interactions between two defective MoO 3−x layers, leading to a capacitor-like interlayer diffusion reaching a large capacity of 426 C g −1 on the surface of the amorphous layer and a diffusion-controlled intralayer diffusion of 546 C g −1 within the amorphous layer. These characteristics optimize Li-ion storage kinetics while achieving full capacities of amorphous materials with high stability. This work might offer a feasible platform of 2D non-vdW heterostructures for boosting and understanding Li-ion storage performance.

CAS / MDL: 7789-24-4 10241-05-1
研究领域: 材料科学 · 能源科学 · 计算化学
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

ZIF-67/Ti3C2 MXene intercalated membrane with enhanced physical/chemical coupling light-to-heat conversion for laser ignition

Yingnan Yang,Haifeng Yang,Pengfei Tang,Xiaodong Li,Weimiao Wang,Guangcheng Yang

Laser induced high temperature pulse (HTP) generation has been widely used in some high-immediacy applications requiring dramatic temperature changes. Recent years researchers put interest in light-to-heat (include photothermal, light induced exothermic reaction and combination of both) materials to reduce the initiating energy of the laser ignition. However, the laser energy for realizing sufficient light-to-heat conversion is still high. MXene exhibits excellent light absorption, high light-to-heat conversion efficiency and has abundant metastable atoms which trend to undergo exothermic chemical reactions, but its incomplete oxidation affects its total heat release when the laser power is relatively high. Herein, we have prepared a ZIF-67/Ti 3 C 2 MXene intercalated membrane. It is found that porous ZIF-67 exhibits a synergistic effect on MXene and can significantly improve its physical/chemical coupled HTP by enhancing its light absorption and subsequent energy release during its oxidation. ε 2,4,6,8,10,12-(hexanitrohexaaza) cyclododecane (ε-CL-20) laser ignition experiments prove that ZIF-67/Ti 3 C 2 MXene intercalated membrane exhibits better ignition performance than pure MXene membrane by reducing both ignition threshold (151.2 mJ) and ignition delay (21 ms) at a low laser power intensity (59.7 W/cm 2 ). This work can provide an insight for the structural design of new light-to-heat membranes.

CAS / MDL: 10026-22-9
研究领域: 材料科学 · 光学工程 · 能源与动力工程
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Au nanoparticles decorated flower-like SnS2/Ti3C2 MXene microcomposite for high performance NO2 sensing at room temperature

Wenlei Zhang,Weiheng Wang,Yunfan Wang,Lei Sun,Yongjiao Sun,Jie Hu

The continuous discharging of nitrogen dioxide (NO 2 ) significantly damaged global environment and human health. In this study, SnS 2 microflowers/Ti 3 C 2 MXene heterostructure was modified by Au nanoparticles (AuNPs) for the detection of NO 2 at room temperature. The microcomposite decorated with 6 wt% AuNPs exhibited excellent sensing properties including response value of 5.34 to 1 ppm NO 2 , which was almost 5 times higher than that of undecorated one. The limit of detection lowered from 500 ppb to 5 ppb with the addition of AuNPs. Besides, the AuNPs decorated SnS 2 /MXene microcomposite revealed good selectivity, fatigue resistance, as well as potential application towards flexible sensing. The NO 2 gas sensing mechanism of AuNPs decorated with SnS 2 /Ti 3 C 2 MXene microcomposite was discussed through density functional theory calculation on adsorption behavior and transferred charges in detail. This work may provide an important pathway for the future development of NO 2 sensors at room temperature.

CAS / MDL: 6132-04-3
研究领域: 材料科学 · 环境科学
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CHEMOSPHERE · 2021 · IF 7.086

High-throughput screening and spatial profiling of low-mass pesticides using a novel Ti3C2 MXene nanowire (TMN) as MALDI MS matrix

Chunxia Ma,Xiao Wang,Huamin Zhang,Wei Liu,Daijie Wang,Feng Liu,Heng Lu,Luqi Huang

Pesticides play critical roles in agricultural fields; however, pesticide residues can cause serious damage to human health and the ecological environment; therefore, developing a rapid and sensitive method for pesticide detection is urgently needed. Nanostructure-assisted matrix laser desorption/ionization (MALDI) mass spectrometry (MS) has great potential for the detection of low-mass pesticides. In this study, a novel Ti 3 C 2 MXene nanowire (TMN) was prepared by a facile sol-gel method and served as a matrix to enhance MALDI MS performance in the analysis of pesticides in positive ion mode. The TMN showed superior performance in the high-throughput detection of six kinds of pesticides (organophosphorus, organochlorine , carbamate, neonicotinoids, triazole, and oxadiazines), with ultrahigh sensitivity (detection limits at sub-ppt levels), remarkable repeatability, excellent salt tolerance, and extremely low background compared to traditional organic matrices due to the specific polyaromatic structure and the doping of nitrogen. Furthermore, this matrix was successfully employed for the analysis of residual pesticides in traditional Chinese herbs, and the level of diniconazole was quantified with a linear range of 0–50 ng/mL (R 2  > 0.99). More importantly, the spatial distribution of various endogenous compounds (e.g., amino acids and saccharides, fatty acids, alkaloids, and plant hormones) and xenobiotic pesticides from the intact root of the medicinal plant P. quinquefolium was clearly visualized using the TMN self-assembly film as a matrix for MALDI imaging mass spectrometry (IMS). With superior advantages such as sensitivity, simplicity, rapidness, and minimal sample requirement, TMN as a matrix-assisted MALDI MS shows great promise for various applications.

CAS / MDL: 64-17-5
研究领域: 分析化学 · 环境科学 · 药学
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JOURNAL OF HAZARDOUS MATERIALS · 2022 · IF 14.224

Ternary heterostructures of 1D/2D/2D CuCo2S4/CuS/Ti3C2 MXene: Boosted amperometric sensing for chlorpyrifos

Yuping Mi,Yisong Zhao,Jianmin Chen,Xiaolu Li,Yunxia Yang,Faming Gao

Multicomponent heterogeneous Ti 3 C 2 transition metal carbide (MXene)-based materials are receiving extensive research attention due to their interesting synergistic interactions and catalytic properties. However, the morphology-controllable synthesis of heterostructures as structural stabilizers for Ti 3 C 2 MXene remains a challenge owing the complicated synthesis procedure. In this work, a kind of ternary heterogeneous nanomaterials CuCo 2 S 4 /CuS/Ti 3 C 2 MXene with a nanorod/nanoplate/nanosheet hybrid architecture is constructed through a one-step low-temperature solvothermal method. The well-designed ternary one-dimensional (1D)/two-dimensional (2D)/2D CuCo 2 S 4 /CuS/Ti 3 C 2 MXene heteromaterials exhibit synergistic improvements in substrate-catalyzed reactions for electrochemical acetylcholinesterase (AChE) biosensor . The Michaelis-Menten constant for the Nafion/AChE/CuCo 2 S 4 /CuS/Ti 3 C 2 MXene/GCE biosensor is 228 μM, which is smaller than ones reported in previous literatures, indicating a higher affinity of the fabricated enzyme biosensor to acetylthiocholine chloride. The biosensor exhibits a well linear relationship with chlorpyrifos concentration ranging from 2.852 × 10 −12 M to 2.852 × 10 −6 M. The multicomponent 1D/2D/2D CuCo 2 S 4 /CuS/Ti 3 C 2 MXene heteromaterial may shine a light in more electrochemical applications.

研究领域: 材料科学 · 分析化学 · 环境科学
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Journal of Water Process Engineering · 2024 · IF 6.3

Interface engineering of Ti3C2 MXene assisted anatase/rutile TiO2 with hetero-phase junction for enhancing the photocatalytic activity of tetracycline hydrochloride removal and H2 production

Jianan Dai,Chao Wu,Jing Ma,Shu-Hao Chang,Weiwei Liu

The conventional heterojunction formed by combining two different semiconductors is associated with issues of low compatibility, restricted intimate contact, and limited charge anti-recombination process. To address these issues, a simple strategy was adopted to fabricate a hetero-phase junction flanked with two dissimilar crystal phases of a single semiconducting material . This study employed TiB 2 as the initial material to fabricate an anatase/rutile TiO 2 hetero-phase junction material (AR-TiO 2 ), followed by its combination with highly conductive monolayer Ti 3 C 2 nanosheets to develop an AR-TiO 2 /Ti 3 C 2 composite photocatalyst . The photocatalyst displayed a wide range of light absorption and a remarkable capability for separating photogenerated carriers. The closely interconnected hetero-phase junction surface, formed by the rutile and anatase phases of AR-TiO 2 , combined with the incorporation of highly conductive Ti 3 C 2 nanosheets , synergistically increased the availability of multi-dimensional active sites and increased the efficacy of separating photogenerated electron pairs. The optimized AR-TiO 2 /Ti 3 C 2 achieved a degradation efficiency of 91.49 % for tetracycline hydrochloride (TCH) within 2 h and produced 1005.81 μmol of hydrogen in 6 h. The impacts of initial pH, co-existing anions, initial TCH concentration, initial temperature, and various pollutant species on the catalytic efficiency were also investigated. pH was shown to have the greatest impact on the photocatalytic performance of AR-TiO 2 /Ti 3 C 2 for TCH degradation. •O 2 − , and h + were identified as the primary reactive species that enabled the photocatalytic performance of AR-TiO 2 /Ti 3 C 2 through trapping experiments. This study presents a novel method to synthesize hetero-phase junction photocatalysts and suggests that Ti 3 C 2 has potential prospects for use in photocatalysis .

CAS / MDL: 12045-63-5
研究领域: 材料科学 · 环境科学
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