Mxene Quantum(Mxene 量子)研究综述
Mxene Quantum Mxene 量子 - In the present work, a kind of fluorescent MXene quantum dots (MQDs) was synthesized via an intermittent ultrasound process using N,N-dimethyl formamide as solvent. [1] Here, to explore their new properties and expand biological applications, chlorine and nitrogen co-doped Ti3C2 MXene quantum dots (Cl, N-Ti3C2 MQDs) were designed and synthesized, and their hydroxyl radical scavenging properties were investigated for the first time, revealing outstanding performance. [2] MXene quantum dots feature favorable biological compatibility and superior optical properties, offering great potential for biomedical applications such as reactive oxygen species (ROS) scavenging and fluorescence sensing. [3] MXene quantum dots (MQDs) derived from MXene with photoluminescent properties have attracted considerable attention. [4] Nickel@MXene quantum dots (Ni@MQDs), as novel flower-like hybrid materials, were firstly prepared through a simple reduction method. [5] In the present study, density functional theory was utilized to investigate the electronic structure and hydrogen evolution performance of Ti3C2O2 MXene quantum dots/graphene (QDs/G) heterostructure. [6] Herein, we focused on five types of quantum dots (Cd-containing quantum dots, CuInS2 quantum dots, black phosphorus quantum dots, MXene quantum dots, and carbon-based quantum dots) for cell imaging and their toxicity in vivo and in vitro. [7] Herein, we report on the synthesis and characterization of plasmonic gold nanorods (NRs) in situ decorated onto the Ti3C2 MXene quantum dots-interspersed Ti3C2 nanosheet (TDTS) as well as their implementation as photoanodes for full-spectrum solar-light-activated PEC water splitting. [8] As an example application, we show that the high-purity MXene quantum dots produced using this room-temperature chemical-free synthesis method exhibit superior performance as electrode materials for electrochemical sensing of hydrogen peroxide compared to the highly oxidized samples obtained through conventional hydrothermal synthesis. [9] A novel label-free surface plasmon resonance (SPR) aptasensor has been constructed for the detection of N-gene of SARS-CoV-2 by using thiol-modified niobium carbide MXene quantum dots (Nb2C-SH QDs) as the bioplatform for anchoring N-gene-targeted aptamer. [10] MXene quantum dots (MQDs) were anchored on the surface of Ni–Co LDH via the surface spatial confinement effect to boost the electrochemical activity and stability. [11] The fluorescence emission of Ti 3 C 2 MXene quantum dots (Ti 3 C 2 MQDs) is in the range 350–600 nm, and the maximum emission peak is at 430 nm that overlaps with the UV absorption of curcumin at 430 nm to a large extent. [12] The titanium carbide (Ti3C2Tx)-MXene quantum dot-modified SnO2 (MQDs-SnO2) ETL was found to be able to rapidly induce perovskite nucleation from the precursor solution, forming an intermediate perovskite phase upon anti-solvent treatment. [13] MXene quantum dots have attracted much attention due to their great optical performance and excellent water solubility. [14] The deprotonated Ti3C2 MXene quantum dots (Ti3C2 MQDs) exhibit excitation wavelength-dependent blue photoluminescence with typical excitation/emission peaks at 330/415 nm and a quantum yield of 22% due to strong quantum confinement. [15] Multiple-color emissive MXene quantum dots (MQDs) exhibit vast application prospects in various fields, including optoelectronics, bioimaging, and catalysis. [16] Herein, we designed a near-infrared (NIR) photothermal immunoassay for the qualitative or quantitative detection of prostate-specific antigen (PSA) using titanium carbide (Ti3C2) MXene quantum dot (QD)-encapsulated liposomes with high photothermal efficiency. [17] Here, the first use of 0D titanium carbide (Ti3 C2 ) MXene quantum dots (MQDs) for immunomodulation is presented with the goal of enhancing material-based tissue repair after injury. [18] MXene quantum dots, a novel 1D material with high pseudocapacitance, are engineered on MPG through in-situ electrochemical deposition. [19] Herein, Ti3C2 MXene quantum dots (QDs) possess the activity of Pt as co-catalyst in promotion the photocatalytic H2 evolution to form heterostructure with g-C3N4 nanosheets (NSs) (denoted as g-C3N4@Ti3C2 QDs). [20] Here, a white laser with V2 C MXene quantum dots (MQDs) is originally demonstrated by constructing a broadband nonlinear random scattering system with enhanced gain. [21]在本工作中，以 N,N-二甲基甲酰胺为溶剂，通过间歇超声工艺合成了一种荧光 MXene 量子点 (MQD)。 [1] 在这里，为了探索它们的新特性并扩大生物应用，设计并合成了氯和氮共掺杂的 Ti3C2 MXene 量子点（Cl, N-Ti3C2 MQDs），并首次研究了它们的羟基自由基清除性能，揭示了出色的表现。 [2] MXene 量子点具有良好的生物相容性和优异的光学特性，为活性氧 (ROS) 清除和荧光传感等生物医学应用提供了巨大潜力。 [3] 源自具有光致发光特性的 MXene 的 MXene 量子点 (MQD) 引起了相当大的关注。 [4] 镍@MXene量子点（Ni@MQDs）作为一种新型的花状杂化材料，首先通过简单的还原方法制备。 [5] 在本研究中，利用密度泛函理论研究了 Ti3C2O2 MXene 量子点/石墨烯 (QDs/G) 异质结构的电子结构和析氢性能。 [6] 在此，我们重点研究了五种用于细胞成像的量子点（含镉量子点、CuInS2 量子点、黑磷量子点、MXene 量子点和碳基量子点）及其在体内和体外的毒性。 [7] 在此，我们报告了在 Ti3C2 MXene 量子点散布的 Ti3C2 纳米片 (TDTS) 上原位装饰的等离子金纳米棒 (NRs) 的合成和表征，以及它们作为全光谱太阳光激活 PEC 水的光阳极的应用。分裂。 [8] 作为一个示例应用，我们表明，与通过传统水热合成获得的高度氧化的样品相比，使用这种室温无化学合成方法生产的高纯度 MXene 量子点作为过氧化氢电化学传感电极材料表现出优异的性能。 [9] 以硫醇修饰的碳化铌 MXene 量子点 (Nb2C-SH QDs) 作为锚定 N -基因靶向适体。 [10] MXene 量子点 (MQD) 通过表面空间限制效应锚定在 Ni-Co LDH 的表面，以提高电化学活性和稳定性。 [11] Ti 3 C 2 MXene 量子点（Ti 3 C 2 MQDs）的荧光发射在 350-600 nm 范围内，最大发射峰在 430 nm，与姜黄素在 430 nm 的紫外吸收重叠至较大程度。 [12] 碳化钛 (Ti3C2Tx)-MXene 量子点改性的 SnO2 (MQDs-SnO2) ETL 被发现能够从前体溶液中快速诱导钙钛矿成核，在反溶剂处理后形成中间钙钛矿相。 [13] MXene量子点因其出色的光学性能和优异的水溶性而备受关注。 [14] 去质子化的 Ti3C2 MXene 量子点 (Ti3C2 MQD) 表现出与激发波长相关的蓝色光致发光，在 330/415 nm 处具有典型的激发/发射峰，由于强量子限制，量子产率为 22%。 [15] 多色发射 MXene 量子点 (MQD) 在光电子学、生物成像和催化等各个领域具有广阔的应用前景。 [16] 在此，我们设计了一种近红外 (NIR) 光热免疫测定法，用于使用具有高光热效率的碳化钛 (Ti3C2) MXene 量子点 (QD) 封装的脂质体对前列腺特异性抗原 (PSA) 进行定性或定量检测。 [17] 在这里，首次使用 0D 碳化钛 (Ti3 C2 ) MXene 量子点 (MQD) 进行免疫调节，目的是增强损伤后基于材料的组织修复。 [18] MXene 量子点是一种具有高赝电容的新型一维材料，通过原位电化学沉积在 MPG 上设计。 [19] 在此，Ti3C2 MXene 量子点 (QDs) 具有 Pt 作为助催化剂的活性，可促进光催化 H2 释放以与 g-C3N4 纳米片 (NSs) 形成异质结构（表示为 g-C3N4@Ti3C2 QDs）。 [20] 在这里，最初通过构建具有增强增益的宽带非线性随机散射系统来演示具有 V2 C MXene 量子点 (MQD) 的白色激光器。 [21]
Ti3c2 Mxene Quantum Ti3c2 Mxene 量子
Here, to explore their new properties and expand biological applications, chlorine and nitrogen co-doped Ti3C2 MXene quantum dots (Cl, N-Ti3C2 MQDs) were designed and synthesized, and their hydroxyl radical scavenging properties were investigated for the first time, revealing outstanding performance. [1] Herein, we report on the synthesis and characterization of plasmonic gold nanorods (NRs) in situ decorated onto the Ti3C2 MXene quantum dots-interspersed Ti3C2 nanosheet (TDTS) as well as their implementation as photoanodes for full-spectrum solar-light-activated PEC water splitting. [2] The deprotonated Ti3C2 MXene quantum dots (Ti3C2 MQDs) exhibit excitation wavelength-dependent blue photoluminescence with typical excitation/emission peaks at 330/415 nm and a quantum yield of 22% due to strong quantum confinement. [3] Herein, Ti3C2 MXene quantum dots (QDs) possess the activity of Pt as co-catalyst in promotion the photocatalytic H2 evolution to form heterostructure with g-C3N4 nanosheets (NSs) (denoted as g-C3N4@Ti3C2 QDs). [4]在这里，为了探索它们的新特性并扩大生物应用，设计并合成了氯和氮共掺杂的 Ti3C2 MXene 量子点（Cl, N-Ti3C2 MQDs），并首次研究了它们的羟基自由基清除性能，揭示了出色的表现。 [1] 在此，我们报告了在 Ti3C2 MXene 量子点散布的 Ti3C2 纳米片 (TDTS) 上原位装饰的等离子金纳米棒 (NRs) 的合成和表征，以及它们作为全光谱太阳光激活 PEC 水的光阳极的应用。分裂。 [2] 去质子化的 Ti3C2 MXene 量子点 (Ti3C2 MQD) 表现出与激发波长相关的蓝色光致发光，在 330/415 nm 处具有典型的激发/发射峰，由于强量子限制，量子产率为 22%。 [3] 在此，Ti3C2 MXene 量子点 (QDs) 具有 Pt 作为助催化剂的活性，可促进光催化 H2 释放以与 g-C3N4 纳米片 (NSs) 形成异质结构（表示为 g-C3N4@Ti3C2 QDs）。 [4]
mxene quantum dot Mxene 量子点
In the present work, a kind of fluorescent MXene quantum dots (MQDs) was synthesized via an intermittent ultrasound process using N,N-dimethyl formamide as solvent. [1] Here, to explore their new properties and expand biological applications, chlorine and nitrogen co-doped Ti3C2 MXene quantum dots (Cl, N-Ti3C2 MQDs) were designed and synthesized, and their hydroxyl radical scavenging properties were investigated for the first time, revealing outstanding performance. [2] MXene quantum dots feature favorable biological compatibility and superior optical properties, offering great potential for biomedical applications such as reactive oxygen species (ROS) scavenging and fluorescence sensing. [3] MXene quantum dots (MQDs) derived from MXene with photoluminescent properties have attracted considerable attention. [4] Nickel@MXene quantum dots (Ni@MQDs), as novel flower-like hybrid materials, were firstly prepared through a simple reduction method. [5] In the present study, density functional theory was utilized to investigate the electronic structure and hydrogen evolution performance of Ti3C2O2 MXene quantum dots/graphene (QDs/G) heterostructure. [6] Herein, we focused on five types of quantum dots (Cd-containing quantum dots, CuInS2 quantum dots, black phosphorus quantum dots, MXene quantum dots, and carbon-based quantum dots) for cell imaging and their toxicity in vivo and in vitro. [7] Herein, we report on the synthesis and characterization of plasmonic gold nanorods (NRs) in situ decorated onto the Ti3C2 MXene quantum dots-interspersed Ti3C2 nanosheet (TDTS) as well as their implementation as photoanodes for full-spectrum solar-light-activated PEC water splitting. [8] As an example application, we show that the high-purity MXene quantum dots produced using this room-temperature chemical-free synthesis method exhibit superior performance as electrode materials for electrochemical sensing of hydrogen peroxide compared to the highly oxidized samples obtained through conventional hydrothermal synthesis. [9] A novel label-free surface plasmon resonance (SPR) aptasensor has been constructed for the detection of N-gene of SARS-CoV-2 by using thiol-modified niobium carbide MXene quantum dots (Nb2C-SH QDs) as the bioplatform for anchoring N-gene-targeted aptamer. [10] MXene quantum dots (MQDs) were anchored on the surface of Ni–Co LDH via the surface spatial confinement effect to boost the electrochemical activity and stability. [11] The fluorescence emission of Ti 3 C 2 MXene quantum dots (Ti 3 C 2 MQDs) is in the range 350–600 nm, and the maximum emission peak is at 430 nm that overlaps with the UV absorption of curcumin at 430 nm to a large extent. [12] The titanium carbide (Ti3C2Tx)-MXene quantum dot-modified SnO2 (MQDs-SnO2) ETL was found to be able to rapidly induce perovskite nucleation from the precursor solution, forming an intermediate perovskite phase upon anti-solvent treatment. [13] MXene quantum dots have attracted much attention due to their great optical performance and excellent water solubility. [14] The deprotonated Ti3C2 MXene quantum dots (Ti3C2 MQDs) exhibit excitation wavelength-dependent blue photoluminescence with typical excitation/emission peaks at 330/415 nm and a quantum yield of 22% due to strong quantum confinement. [15] Multiple-color emissive MXene quantum dots (MQDs) exhibit vast application prospects in various fields, including optoelectronics, bioimaging, and catalysis. [16] Herein, we designed a near-infrared (NIR) photothermal immunoassay for the qualitative or quantitative detection of prostate-specific antigen (PSA) using titanium carbide (Ti3C2) MXene quantum dot (QD)-encapsulated liposomes with high photothermal efficiency. [17] Here, the first use of 0D titanium carbide (Ti3 C2 ) MXene quantum dots (MQDs) for immunomodulation is presented with the goal of enhancing material-based tissue repair after injury. [18] MXene quantum dots, a novel 1D material with high pseudocapacitance, are engineered on MPG through in-situ electrochemical deposition. [19] Herein, Ti3C2 MXene quantum dots (QDs) possess the activity of Pt as co-catalyst in promotion the photocatalytic H2 evolution to form heterostructure with g-C3N4 nanosheets (NSs) (denoted as g-C3N4@Ti3C2 QDs). [20] Here, a white laser with V2 C MXene quantum dots (MQDs) is originally demonstrated by constructing a broadband nonlinear random scattering system with enhanced gain. [21]在本工作中，以 N,N-二甲基甲酰胺为溶剂，通过间歇超声工艺合成了一种荧光 MXene 量子点 (MQD)。 [1] 在这里，为了探索它们的新特性并扩大生物应用，设计并合成了氯和氮共掺杂的 Ti3C2 MXene 量子点（Cl, N-Ti3C2 MQDs），并首次研究了它们的羟基自由基清除性能，揭示了出色的表现。 [2] MXene 量子点具有良好的生物相容性和优异的光学特性，为活性氧 (ROS) 清除和荧光传感等生物医学应用提供了巨大潜力。 [3] 源自具有光致发光特性的 MXene 的 MXene 量子点 (MQD) 引起了相当大的关注。 [4] 镍@MXene量子点（Ni@MQDs）作为一种新型的花状杂化材料，首先通过简单的还原方法制备。 [5] 在本研究中，利用密度泛函理论研究了 Ti3C2O2 MXene 量子点/石墨烯 (QDs/G) 异质结构的电子结构和析氢性能。 [6] 在此，我们重点研究了五种用于细胞成像的量子点（含镉量子点、CuInS2 量子点、黑磷量子点、MXene 量子点和碳基量子点）及其在体内和体外的毒性。 [7] 在此，我们报告了在 Ti3C2 MXene 量子点散布的 Ti3C2 纳米片 (TDTS) 上原位装饰的等离子金纳米棒 (NRs) 的合成和表征，以及它们作为全光谱太阳光激活 PEC 水的光阳极的应用。分裂。 [8] 作为一个示例应用，我们表明，与通过传统水热合成获得的高度氧化的样品相比，使用这种室温无化学合成方法生产的高纯度 MXene 量子点作为过氧化氢电化学传感电极材料表现出优异的性能。 [9] 以硫醇修饰的碳化铌 MXene 量子点 (Nb2C-SH QDs) 作为锚定 N -基因靶向适体。 [10] MXene 量子点 (MQD) 通过表面空间限制效应锚定在 Ni-Co LDH 的表面，以提高电化学活性和稳定性。 [11] Ti 3 C 2 MXene 量子点（Ti 3 C 2 MQDs）的荧光发射在 350-600 nm 范围内，最大发射峰在 430 nm，与姜黄素在 430 nm 的紫外吸收重叠至较大程度。 [12] 碳化钛 (Ti3C2Tx)-MXene 量子点改性的 SnO2 (MQDs-SnO2) ETL 被发现能够从前体溶液中快速诱导钙钛矿成核，在反溶剂处理后形成中间钙钛矿相。 [13] MXene量子点因其出色的光学性能和优异的水溶性而备受关注。 [14] 去质子化的 Ti3C2 MXene 量子点 (Ti3C2 MQD) 表现出与激发波长相关的蓝色光致发光，在 330/415 nm 处具有典型的激发/发射峰，由于强量子限制，量子产率为 22%。 [15] 多色发射 MXene 量子点 (MQD) 在光电子学、生物成像和催化等各个领域具有广阔的应用前景。 [16] 在此，我们设计了一种近红外 (NIR) 光热免疫测定法，用于使用具有高光热效率的碳化钛 (Ti3C2) MXene 量子点 (QD) 封装的脂质体对前列腺特异性抗原 (PSA) 进行定性或定量检测。 [17] 在这里，首次使用 0D 碳化钛 (Ti3 C2 ) MXene 量子点 (MQD) 进行免疫调节，目的是增强损伤后基于材料的组织修复。 [18] MXene 量子点是一种具有高赝电容的新型一维材料，通过原位电化学沉积在 MPG 上设计。 [19] 在此，Ti3C2 MXene 量子点 (QDs) 具有 Pt 作为助催化剂的活性，可促进光催化 H2 释放以与 g-C3N4 纳米片 (NSs) 形成异质结构（表示为 g-C3N4@Ti3C2 QDs）。 [20] 在这里，最初通过构建具有增强增益的宽带非线性随机散射系统来演示具有 V2 C MXene 量子点 (MQD) 的白色激光器。 [21]