quantum dot

量子点
  • 文章类型: Journal Article
    电荷注入动力学的原位表征,平衡浓度,和电场分布揭示了量子点发光二极管(QD-LED)的关键机制。在这项工作中,我们开发了电激发瞬态吸收光谱,可以提供上述关键信息,研究QD-LED的效率滚降。我们发现,当QD-LED表现出效率滚降时,每个QD的平均电子数量较低,排除俄歇重组为主要原因。我们还发现,正向偏置下QD层内部的弱电场对效率的影响可以忽略不计。有趣的是,我们发现,随着电压的增加,QD层中的电子浓度在非常低的水平上饱和。当与伴随的效率滚降相结合时,我们认为电子泄漏是驱动电压升高时的主要损失。我们进一步证明,使用ZnS壳层增加电子限制电势使我们能够有效地减轻效率滚降。
    In situ characterizations of charge injection dynamics, equilibrated concentration, and electric field distributions shed light on the critical mechanisms of quantum dot light-emitting diodes (QD-LEDs). In this work, we developed electrically excited transient absorption spectroscopy, which can provide the above key information, to investigate the efficiency roll-off of QD-LEDs. We found that the average electron populations per QD are low when QD-LEDs exhibit efficiency roll-off, excluding Auger recombination as the main cause. We also revealed that the weak electrical field inside the QD layer under forward biases has a negligible impact on the efficiency. Interestingly, we found that as the voltage increases the electron concentration in the QD layer saturates at very low levels. When combined with the concomitant efficiency roll-off, we propose electron leakage is the main loss at elevated driving voltages. We further demonstrate that increasing the electron confinement potential with the ZnS shell enables us to efficiently mitigate the efficiency roll-off.
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  • 文章类型: Journal Article
    硒化铜铟(CISe)是一种原型红外半导体,具有低毒性和独特的光学特性。其量子点(QD)容纳了大量的固有点缺陷,这些缺陷可能积极参与其相当复杂的光物理过程。我们合成了具有相似尺寸但具有明显高度化学计量偏差的原子比的zeCISeQD。使用富Se前体的合成条件产生具有特殊光物理性质的缺CuCISeQD。当Cu与In的比例降低时,光致发光表现出从680到775nm的单调红移。发现发光源于铜空位和反位缺陷。TheCISeQD在5.6、6.9和8.7THz处表现出拉曼活性,分别分配给Cu-Se和In-Se光学声子模式和表面模式。
    Copper indium selenide (CISe) is a prototype infrared semiconductor with low toxicity and unique optical characteristics. Its quantum dots (QDs) accommodate ample intrinsic point defects which may actively participate in their rather complex photophysical processes. We synthesize CISe QDs with similar sizes but with distinct highly stoichiometry-deviating atomic ratios. The synthesis condition employing Se-rich precursors yields the Cu-deficient CISe QDs with special photophysical properties. The photoluminescence exhibits monotonic red shift from 680 to 775 nm when the ratio of Cu\'s proportion to In\'s decreases. The luminescence is found to stem from the copper vacancy and antisite defects. The CISe QDs exhibit Raman activity at 5.6, 6.9, and 8.7 THz that is separately assigned to Cu-Se and In-Se optical phonon modes and surface mode.
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  • 文章类型: Journal Article
    核酸检测在疾病的准确诊断中起着举足轻重的作用。CRISPR/Cas检测系统,因其在各种应用中的重要用途而闻名,通常需要增强的灵敏度或特定的信号放大策略,特别是用于检测低丰度的生物标志物。在这项研究中,我们提出了一种量子点编码珠子(QDB)激活的基于CRISPR/Cas12的侧流测定(QDB-CRISPR-LFA)。这种方法可以实现无扩增,敏感,和BRCA-1的快速检测(<40分钟)。我们使用设计的参考样品和从肿瘤细胞中提取的核酸验证了我们的方法。QDB-CRISPR-LFA提供了一个可视化的,更快速替代传统的BRCA-1实时RT-PCR检测。重要的是,通过整合CRISPR的特异性和QDB的高信号输出,BRCA-1的检测阈值已降低到毫微微水平,表示比现有的CRISPR/Cas检测方法增强2-4个数量级。这一进步强调了我们的方法在推进核酸检测技术方面的潜力,这对于疾病的早期和精确诊断至关重要。
    Nucleic acid detection plays a pivotal role in the accurate diagnosis of diseases. The CRISPR/Cas detection system, noted for its significant utility in a variety of applications, often necessitates enhanced sensitivity or specific signal amplification strategies, particularly for detecting low-abundance biomarkers. In this study, we present a quantum-dot-encoded beads (QDB)-energized CRISPR/Cas12-based lateral-flow assay (QDB-CRISPR-LFA). This method enables amplification-free, sensitive, and rapid detection (<40 min) of BRCA-1. We validated our method using contrived reference samples and nucleic acids extracted from tumor cells. The QDB-CRISPR-LFA provides a visual, more rapid alternative to the traditional BRCA-1 real-time RT-PCR assay. Significantly, through the integration of CRISPR\'s specificity and the high signal output of QDB, the detection threshold for BRCA-1 has been reduced to the femtomolar level, representing an enhancement of 2-4 orders of magnitude over existing CRISPR/Cas detection methods. This advancement underscores the potential of our approach in advancing nucleic acid detection techniques, which is crucial for the early and precise diagnosis of diseases.
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  • 文章类型: Journal Article
    基于肌动蛋白和微管(MT)的运输系统对于细胞内运输至关重要。在甲型流感病毒(IAV)感染期间,MTs为病毒向细胞核贩运提供了很长的踪迹。然而,肌动蛋白细胞骨架在IAV进入,特别是转运过程中的作用仍然不明确。这里,通过使用基于量子点的单病毒跟踪,结果表明,肌动蛋白细胞骨架对于通过网格蛋白介导的内吞作用(CME)进入病毒至关重要。通过CME进入后,病毒通过三种不同的途径到达MTs:病毒(1)由肌球蛋白VI驱动,沿着肌动蛋白丝移动,到达MTs(AF);(2)由Arp2/3依赖性机制组装的肌动蛋白尾推动,到达MTs(AT);(3)直接到达MTs,而没有发生与肌动蛋白相关的运动(NA).因此,NA途径是病毒到达MTs的主要途径,也是最快的途径。只有当大量病毒进入细胞时,AT途径才被激活。通过AF和AT途径运输的病毒具有相似的移动速度,持续时间,和流离失所。这项研究全面可视化了肌动蛋白细胞骨架在IAV进入和运输中的作用,揭示IAV进入后到达MTs的不同途径。该结果对于全球了解IAV感染和细胞内吞转运途径具有重要意义。
    Actin- and microtubule (MT)-based transport systems are essential for intracellular transport. During influenza A virus (IAV) infection, MTs provide long tracks for virus trafficking toward the nucleus. However, the role of the actin cytoskeleton in IAV entry and especially the transit process is still ambiguous. Here, by using quantum dot-based single-virus tracking, it was revealed that the actin cytoskeleton was crucial for the virus entry via clathrin-mediated endocytosis (CME). After entry via CME, the virus reached MTs through three different pathways: the virus (1) was driven by myosin VI to move along actin filaments to reach MTs (AF); (2) was propelled by actin tails assembled by an Arp2/3-dependent mechanism to reach MTs (AT); and (3) directly reached MTs without experiencing actin-related movement (NA). Therefore, the NA pathway was the main one and the fastest for the virus to reach MTs. The AT pathway was activated only when plenty of viruses entered the cell. The viruses transported by the AF and AT pathways shared similar moving velocities, durations, and displacements. This study comprehensively visualized the role of the actin cytoskeleton in IAV entry and transport, revealing different pathways for IAV to reach MTs after entry. The results are of great significance for globally understanding IAV infection and the cellular endocytic transport pathway.
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  • 文章类型: Journal Article
    在这项研究中,已经研究了人类血红蛋白与具有成本效益和化学制造的CdS量子点(QDs)(平均尺寸≈3nm)的相互作用。半导体QD在445nm处显示出最大的可见吸收,激子形成和带隙为≈2.88eV,以及六方晶相。QDs-Hb的结合通过电晕形成与基态络合物形成而发生。发现血红素口袋结合和重组的寿命为t1=43分钟和t2=642分钟,分别。Hb的发射猝灭已经表明CdSQD和Hb之间的能量传递很大,Hb的三次变形。结合热力学显示高度放热性质。从TCSPC研究了电晕形成过程中的超快衰减。结果表明,能量转移效率随着量子点浓度的增加而增加,发生最大≈71.5%的能量转移,平均超快寿命从5.45ns到1.51ns不等。从圆二色性光谱中观察到Hb的二级结构随着α螺旋(≈74%至≈51.07%)和β折叠(≈8.63%至≈10.25%)的变化而变形和展开。SAXS光谱表明,与纯Hb(11±0.23nm)相比,CdSQDs-Hb生物缀合物的回转半径随着QDs浓度的增加而增加(高达23±0.45nm),并且Hb变得更加展开。
    In this study, the interaction of the human hemoglobin with cost effective and chemically fabricated CdS quantum dots (QDs) (average sizes ≈3nm) has been investigated. The semiconductor QDs showed maximum visible absorption at 445 nm with excitonic formation and band gap of ≈ 2.88 eV along with hexagonal crystalline phase. The binding of QDs-Hb occurs through corona formation to the ground sate complex formation. The life time of the heme pocket binding and reorganization were found to be t1 = 43 min and t2 = 642 min, respectively. The emission quenching of the Hb has been indicated large energy transfer between CdS QDs and Hb with tertiary deformation of Hb. The binding thermodynamics showed highly exothermic nature. The ultrafast decay during corona formation was studied from TCSPC. The results showed that the energy transfer efficiency increases with the increase of the QDs concentration and maximum ≈71.5 % energy transfer occurs and average ultrafast lifetime varies from 5.45 ns to1.51 ns. The deformation and unfolding of the secondary structure of Hb with changes of the α-helix (≈74 % to ≈51.07 %) and β-sheets (≈8.63 % to ≈10.25 %) have been observed from circular dichroism spectrum. The SAXS spectrum showed that the radius of gyration of CdS QDs-Hb bioconjugate increased (up to 23 ± 0.45 nm) with the increase of the concentration of QDs compare with pure Hb (11 ± 0.23 nm) and Hb becoming more unfolded.
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  • 文章类型: Journal Article
    汞(Hg),一种臭名昭著的重金属,对人类健康和环境有有害影响,需要发展精确的测量方法。这项研究介绍了一种快速,直接的光化学方法来合成巯基乙酸(TGA)稳定的CdTe/CdS/ZnS核/多壳量子点(QD)。利用荧光光谱对合成的CdTe/CdS/ZnS量子点进行了全面表征,透射电子显微镜(TEM),能量色散X射线光谱(EDS),场发射扫描电子显微镜(FESEM),和X射线衍射(XRD)。XRD和EDS结果证实成功形成了CdTe/CdS/ZnS结构。此外,FESEM和TEM结果表明CdTe/CdS/ZnS量子点呈球形。结果表明,在Hg2+离子的存在下,合成的显示出充满活力的绿色荧光和显著的猝灭,这些QD成为制造荧光传感器的有希望的候选者。所提出的传感器对Hg2+表现出显著的灵敏度,检测限为16.32nM,线性范围为20nM至70nM。通过分析各种阴离子和阳离子证实了传感器的选择性。此外,当用自来水测试时,河水,和农业样本,传感器表现出可靠的性能,通过电感耦合等离子体(ICP)分析验证。此外,固定在微垫上的CdTe/CdS/ZnS量子点被证明对现场水样分析有效,为环境监测提供了一个通用的解决方案。
    Mercury (Hg), a notorious heavy metal with detrimental impacts on human health and the environment, necessitates the development of precise measurement methods. This study introduces an expeditious and straightforward photochemical approach to synthesize thioglycolic acid (TGA)-stabilized CdTe/CdS/ZnS core/multi-shell quantum dots (QDs). The synthesized CdTe/CdS/ZnS QDs were comprehensively characterized using fluorescence spectroscopy, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), Field Emission Scanning Electron Microscopy (FESEM), and X-Ray diffraction (XRD). XRD and EDS results confirmed the successful formation of CdTe/CdS/ZnS structure. Also, FESEM and TEM results showed that CdTe/CdS/ZnS QDs were spherical. Results showed that synthesized Exhibiting vibrant green fluorescence and notable quenching in the presence of Hg2+ ions, these QDs emerge as promising candidates for fabricating a fluorescent sensor. The proposed sensor demonstrates notable sensitivity to Hg2+, featuring a detection limit of 16.32 nM and a linear range from 20 nM to 70 nM. The sensor\'s selectivity was confirmed by analyzing various anions and cations. Moreover, when tested with tap water, river water, and agricultural samples, the sensor exhibited reliable performance, validated by Inductively Coupled Plasma (ICP) analysis. Additionally, CdTe/CdS/ZnS QDs immobilized on micro pads proved effective for on-site water sample analysis, presenting a versatile solution for environmental monitoring.
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  • 文章类型: Journal Article
    CdS量子点(CdSQD)由于其对可见光的显着响应以及导带和价带的合适放置而被认为是有前途的光催化剂。然而,光腐蚀问题严重制约了它们的应用。在这里,通过静电自组装方法将Co9S8纳米管负载到CdSQDs上,成功制备了CdSQDs-Co9S8中空纳米管复合光催化剂。实验结果表明,Co9S8助催化剂的引入可以与CdS量子点形成稳定的结构,能有效避免CdS量子点的光腐蚀。与空白CdS量子点相比,CdSQDs-Co9S8复合材料表现出明显更好的光催化析氢性能。特别是,负载30%Co9S8(CdSQDs-30%Co9S8)的CdSQDs表现出最佳的光催化性能,H2生成速率达到9642.7μmol·g-1·h-1,是空白CdS量子点的60.3倍。一系列表征证实,CdS量子点在Co9S8纳米管上的生长有效地促进了光生载流子的分离和迁移,从而提高复合材料的光催化制氢性能。我们期望这项工作将有助于CdS基光催化剂的合理设计,从而能够开发更低成本的产品,用于光催化的高效和高稳定性复合材料。
    CdS quantum dots (CdS QDs) are regarded as a promising photocatalyst due to their remarkable response to visible light and suitable placement of conduction bands and valence bands. However, the problem of photocorrosion severely restricts their application. Herein, the CdS QDs-Co9S8 hollow nanotube composite photocatalyst has been successfully prepared by loading Co9S8 nanotubes onto CdS QDs through an electrostatic self-assembly method. The experimental results show that the introduction of Co9S8 cocatalyst can form a stable structure with CdS QDs, and can effectively avoid the photocorrosion of CdS QDs. Compared with blank CdS QDs, the CdS QDs-Co9S8 composite exhibits obviously better photocatalytic hydrogen evolution performance. In particular, CdS QDs loaded with 30% Co9S8 (CdS QDs-30%Co9S8) demonstrate the best photocatalytic performance, and the H2 production rate reaches 9642.7 μmol·g-1·h-1, which is 60.3 times that of the blank CdS QDs. A series of characterizations confirm that the growth of CdS QDs on Co9S8 nanotubes effectively facilitates the separation and migration of photogenerated carriers, thereby improving the photocatalytic hydrogen production properties of the composite. We expect that this work will facilitate the rational design of CdS-based photocatalysts, thereby enabling the development of more low-cost, high-efficiency and high-stability composites for photocatalysis.
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  • 文章类型: Journal Article
    纳米晶体(NC)自组装成密堆积,有序超晶格(SLs)是广义的,工程兴趣。NCSL中多面体纳米晶体的相干取向增强了电子,磁性,和振动耦合,导致各种紧急现象。这里,我们表明,许多SL中多面体NC的相干取向可以简单地通过考虑其对表面配体构象熵的影响来理解。我们报告了预测的纳米晶体取向和熵驱动力,以定向各种纳米晶体形状和超晶格晶胞,我们表明配体熵足以重现大量报道的实验和计算观察结果。我们还使用该框架来预测定向NCSL中的间隙物质如溶剂或未结合配体的预期分布。这项工作为理解超晶格中NC的方向以及分析多元结构的未来框架提供了直觉。
    The self-assembly of nanocrystals (NCs) into close-packed, ordered superlattices (SLs) is of broad, engineering interest. The coherent orientation of polyhedral nanocrystals within NC SLs enhances electronic, magnetic, and vibrational coupling, leading to a variety of emergent phenomena. Here, we show that coherent orientation of polyhedral NCs in many SLs can be understood simply by considering its effect on the conformational entropy of surface ligands. We report the predicted nanocrystal orientations and entropic driving force to orient for a broad range of nanocrystal shapes and superlattice unit cells, and we show that ligand entropy is sufficient to reproduce a host of reported experimental and computational observations. We additionally use this framework to predict the expected distribution of interstitial species such as solvent or unbound ligands in an oriented NC SL. This work offers intuition for understanding the orientation of NCs in superlattices and a future framework for analyzing multinary structures.
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  • 文章类型: Journal Article
    短波红外(SWIR)发光二极管(LED)已成为光通信等多种应用的有前途的技术,生物医学成像,监视,和机器视觉。胶体量子点(QD)由于其溶液可加工性而对SWIRLED特别有吸引力,与柔性基板的兼容性,和可调吸收和发光。然而,大多数SWIR发射量子点中有毒元素或贵金属的存在会带来健康,环境,和成本挑战。在这种情况下,CuInS2(CIS)量子点是众所周知的低毒性,具有成本效益的制造,和SWIR发光能力。然而,迄今为止,CISQD尚未直接用于制造SWIRLED,这是由于粒子稳定性低,低效的电荷载流子复合,以及集成到LED器件后的显着蓝移发光。为了应对挑战,我们提出了一种使用ZnI2作为化学添加剂的双钝化策略,以增强纯CISQD的光学性能和在LED器件实现时的电荷载流子复合。所得的基于CIS-QD的LED表现出稳定的SWIR电致发光(EL)峰(超过1000nm),具有高EL辐射度,并且在SWIR区域具有记录的外部量子效率。我们的研究代表了SWIR-QLED技术向前迈出的重要一步,为高性能的发展提供了一条途径,低成本,和无毒的SWIR光源。
    Short-wave infrared (SWIR) light-emitting diodes (LEDs) have emerged as promising technologies for diverse applications such as optical communication, biomedical imaging, surveillance, and machine vision. Colloidal quantum dots (QDs) are particularly attractive for SWIR LEDs due to their solution processability, compatibility with flexible substrates, and tunable absorption and luminescence. However, the presence of toxic elements or precious metals in most SWIR-emitting QDs poses health, environmental, and cost challenges. In this context, CuInS2 (CIS) QDs are known for low toxicity, cost-effective fabrication, and SWIR-light emitting capability. However, CIS QDs have not yet been directly utilized to fabricate SWIR LEDs to date, which is due to low particle stability, inefficient charge carrier recombination, and significantly blue-shifted luminescence after integrating into LED devices. To address challenges, we propose a dual-passivation strategy using ZnI2 as a chemical additive to enhance both the optical property of plain CIS QDs and charge carrier recombination upon LED device implementation. The resulting CIS-QD-based LEDs exhibit a stable SWIR electroluminescence (EL) peak (over 1000 nm) with a high EL radiance and a record external quantum efficiency in the SWIR region. Our study represents a significant step forward in SWIR-QLED technology, offering a pathway for the development of high-performance, low-cost, and nontoxic SWIR light sources.
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  • 文章类型: Journal Article
    我们研究了量子点(QD)中的电子隧穿(ET)和局部安德列夫反射(AR)过程,该量子点耦合到具有非共线铁磁的左右铁磁引线。特别是,我们认为QD也侧耦合到在其末端托管Majorana结合态(MBS)的纳米线。我们的结果表明,当MBSs的一个模式同时耦合到QD上的自旋和自旋电子时,中心峰的高度与MBS仅耦合到一个自旋分量电子的高度不同。ET和AR电导,由点-MBS杂交介导,强烈依赖于引线中左右磁矩之间的角度。QD和MBS之间的相互作用将导致角度相关的隧道磁阻的符号变化。这与QD耦合到规则的铁氧体模式的情况非常不同,并可用于检测MBS的存在,当前在凝聚态物理学中的一项挑战正在进行广泛的研究。
    We study the electron tunneling (ET) and local Andreev reflection (AR) processes in a quantum dot (QD) coupled to the left and right ferromagnetic leads with noncollinear ferromagnetisms. In particular, we consider that the QD is also side-coupled to a nanowire hosting Majorana bound states (MBSs) at its ends. Our results show that when one mode of the MBSs is coupled simultaneously to both spin-up and spin-down electrons on the QD, the height of the central peak is different from that if the MBS is coupled to only one spin component electrons. The ET and AR conductances, which are mediated by the dot-MBS hybridization, strongly depend on the angle between the left and right magnetic moments in the leads. Interaction between the QD and the MBSs will result in sign change of the angle-dependent tunnel magnetoresistance. This is very different from the case when the QD is coupled to regular fermonic mode, and can be used for detecting the existence of MBSs, a current challenge in condensed matter physics under extensive investigations.
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