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Light-Triggered Anti-ambipolar Transistor Based on an In-Plane Lateral Homojunction 基于平面内侧同质结的光触发反双极晶体管
IF 10.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-02 DOI: 10.1021/acs.nanolett.4c01679
Hecheng Han, Baoqing Zhang, Zihao Zhang, Yiming Wang, Chuan Liu, Arun Kumar Singh, Aimin Song, Yuxiang Li, Jidong Jin, Jiawei Zhang
Currently, the construction of anti-ambipolar transistors (AATs) is primarily based on asymmetric heterostructures, which are challenging to fabricate. AATs used for photodetection are accompanied by dark currents that prove difficult to suppress, resulting in reduced sensitivity. This work presents light-triggered AATs based on an in-plane lateral WSe2 homojunction without van der Waals heterostructures. In this device, the WSe2 channel is partially electrically controlled by the back gate due to the screening effect of the bottom electrode, resulting in a homojunction that is dynamically modulated with gate voltage, exhibiting electrostatically reconfigurable and light-triggered anti-ambipolar behaviors. It exhibits high responsivity (188 A/W) and detectivity (8.94 × 1014 Jones) under 635 nm illumination with a low power density of 0.23 μW/cm2, promising a new approach to low-power, high-performance photodetectors. Moreover, the device demonstrates efficient self-driven photodetection. Furthermore, ternary inverters are realized using monolithic WSe2, simplifying the manufacturing of multivalued logic devices.
目前,反双极性晶体管(AAT)的制造主要基于非对称异质结构,而非对称异质结构的制造具有挑战性。用于光电探测的反双极型晶体管会伴随着难以抑制的暗电流,从而导致灵敏度降低。这项研究提出了基于无范德华异质结构的面内横向 WSe2 同质结的光触发 AAT。在该器件中,由于底部电极的屏蔽效应,WSe2 沟道部分受背面栅极的电控制,从而形成了一个随栅极电压动态调制的同质结,表现出静电可重构和光触发的反双极行为。在 635 纳米光照下,该器件以 0.23 μW/cm2 的低功率密度实现了高响应率(188 A/W )和高检测率(8.94 × 1014 Jones),有望成为低功耗、高性能光电检测器的一种新方法。此外,该器件还展示了高效的自驱动光电探测功能。此外,利用单片 WSe2 实现了三元反相器,简化了多值逻辑器件的制造。
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引用次数: 0
Ultrasound-Activated PROTAC Prodrugs Overcome Immunosuppression to Actuate Efficient Deep-Tissue Sono-Immunotherapy in Orthotopic Pancreatic Tumor Mouse Models 超声激活的 PROTAC 原药克服免疫抑制,在正位胰腺肿瘤小鼠模型中实现高效的深层组织超声免疫疗法
IF 10.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-02 DOI: 10.1021/acs.nanolett.4c02287
Ye Liu, Haiyang Wang, Mengchao Ding, Wang Yao, Kewei Wang, Ihsan Ullah, Emil Bulatov, Youyong Yuan
The degradation of oncoproteins mediated by proteolysis-targeting chimera (PROTAC) has emerged as a potent strategy in cancer therapy. However, the clinical application of PROTACs is hampered by challenges such as poor water solubility and off-target adverse effects. Herein, we present an ultrasound (US)-activatable PROTAC prodrug termed NPCe6+PRO for actuating efficient sono-immunotherapy in a spatiotemporally controllable manner. Specifically, US irradiation, which exhibits deep-tissue penetration capability, results in Ce6-mediated generation of ROS, facilitating sonodynamic therapy (SDT) and inducing immunogenic cell death (ICD). Simultaneously, the generated ROS cleaves the thioketal (TK) linker through a ROS-responsive mechanism, realizing the on-demand activation of the PROTAC prodrug in deep tissues. This prodrug activation results in the degradation of the target protein BRD4, while simultaneously reversing the upregulation of PD-L1 expression associated with the SDT process. In the orthotopic mouse model of pancreatic tumors, NPCe6+PRO effectively suppressed tumor growth in conjunction with US stimulation.
蛋白水解靶向嵌合体(PROTAC)介导的肿瘤蛋白降解已成为一种有效的癌症治疗策略。然而,PROTACs 的临床应用受到水溶性差和脱靶不良反应等挑战的阻碍。在此,我们提出了一种名为 NPCe6+PRO 的超声(US)可激活 PROTAC 原药,它能以时空可控的方式激活高效的超声免疫疗法。具体来说,具有深层组织穿透能力的超声辐照会导致 Ce6 介导的 ROS 生成,从而促进声动力疗法(SDT)并诱导免疫原性细胞死亡(ICD)。同时,产生的 ROS 会通过 ROS 响应机制裂解硫酮(TK)连接体,实现 PROTAC 原药在深部组织中的按需激活。这种原药活化可导致靶蛋白 BRD4 降解,同时逆转与 SDT 过程相关的 PD-L1 表达上调。在胰腺肿瘤的正位小鼠模型中,NPCe6+PRO 在 US 刺激的同时有效抑制了肿瘤的生长。
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引用次数: 0
Efficient Quasi-2D Perovskite Based Blue Light-Emitting Diodes with Carbon Dots Modified Hole Transport Layer 基于碳点改性空穴传输层的高效准二维过氧化物蓝光发光二极管
IF 10.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-02 DOI: 10.1021/acs.nanolett.4c02110
Hongwei Wang, Baowei Zhang, Boyang Wang, Sai Bai, Liwen Cheng, Yongsheng Hu, Siyu Lu
Quasi-2D perovskites based blue light-emitting diodes (LEDs) suffer from its poor electroluminescence performance, mainly caused by the nonradiative recombination in in defect-rich low-n phases and the unbalanced hole–electron injection in the device. Here, we developed a highly efficient quasi-2D perovskite based sky-blue LEDs behaving recorded external quantum efficiency (EQE) of 21.07% by employing carbon dots (CDs) as additives in the hole transport layer (HTL). We ascribe the high EQE to the effective engineering of CDs: (1) The CDs at the interface of HTLs can suppress the formation of low-efficient n = 1 phase, resulting a high luminescence quantum yield and energy transfer efficiency of the mixed n-phase quasi-2D perovskites. (2) The CDs additives can reduce the conductivity of HTL, partially blocking the hole injection, and thus making more balanced hole–electron injection. The CDs-treated devices have excellent Spectral stability and enhanced operational stability and could be a new alternative additive in the perovskite optoelectronic devices.
基于准二维过氧化物的蓝色发光二极管(LED)存在电致发光性能差的问题,这主要是由富含缺陷的低n相中的非辐射重组和器件中不平衡的空穴-电子注入造成的。在这里,我们通过在空穴传输层(HTL)中使用碳点(CD)作为添加剂,开发出了一种基于准二维过氧化物的高效天蓝色发光二极管,其外部量子效率(EQE)达到了 21.07%。我们将高 EQE 归功于 CD 的有效工程:(1)HTL 接口处的 CD 可以抑制低效率 n = 1 相的形成,从而使混合 n 相准二维过氧化物具有较高的发光量子产率和能量传递效率。(2)CD 添加剂可以降低 HTL 的电导率,部分阻断空穴注入,从而使空穴-电子注入更加平衡。经 CD 处理的器件具有优异的光谱稳定性和更高的工作稳定性,可作为一种新的添加剂用于包晶体光电器件。
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引用次数: 0
In Vivo Exposure Pathways of Ambient Magnetite Nanoparticles Revealed by Machine Learning-Aided Single-Particle Mass Spectrometry 机器学习辅助单颗粒质谱法揭示环境磁铁矿纳米颗粒的体内暴露途径
IF 10.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-02 DOI: 10.1021/acs.nanolett.4c01937
Weican Zhang, Shiwei Huo, Shenxi Deng, Ke Min, Cha Huang, Hang Yang, Lin Liu, Luyao Zhang, Peijie Zuo, Lihong Liu, Qian Liu, Guibin Jiang
Nanosized ultrafine particles (UFPs) from natural and anthropogenic sources are widespread and pose serious health risks when inhaled by humans. However, tracing the inhaled UFPs in vivo is extremely difficult, and the distribution, translocation, and metabolism of UFPs remain unclear. Here, we report a label-free, machine learning-aided single-particle inductively coupled plasma mass spectrometry (spICP-MS) approach for tracing the exposure pathways of airborne magnetite nanoparticles (MNPs), including external emission sources, and distribution and translocation in vivo using a mouse model. Our results provide quantitative analysis of different metabolic pathways in mice exposed to MNPs, revealing that the spleen serves as the primary site for MNP metabolism (84.4%), followed by the liver (11.4%). The translocation of inhaled UFPs across different organs alters their particle size. This work provides novel insights into the in vivo fate of UFPs as well as a versatile and powerful platform for nanotoxicology and risk assessment.
来自自然和人为来源的纳米超细粒子(UFPs)广泛存在,人类吸入后会对健康造成严重危害。然而,在体内追踪吸入的超微粒子极其困难,而且超微粒子的分布、转运和代谢情况仍不清楚。在此,我们报告了一种无标记、机器学习辅助的单颗粒电感耦合等离子体质谱(spICP-MS)方法,该方法利用小鼠模型追踪空气中磁铁矿纳米颗粒(MNPs)的暴露途径(包括外部排放源)以及在体内的分布和转运情况。我们的研究结果对暴露于 MNPs 的小鼠体内的不同代谢途径进行了定量分析,发现脾脏是 MNP 代谢的主要部位(84.4%),其次是肝脏(11.4%)。吸入的超微粒子在不同器官间的转移改变了其粒径。这项工作提供了有关超微粒子体内命运的新见解,并为纳米毒理学和风险评估提供了一个多功能的强大平台。
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引用次数: 0
Imaging Nanomechanical Vibrations and Manipulating Parametric Mode Coupling via Scanning Microwave Microscopy 通过扫描微波显微镜成像纳米机械振动并操纵参数模式耦合
IF 10.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-02 DOI: 10.1021/acs.nanolett.4c01401
Hao Xu, Srisaran Venkatachalam, Toky-Harrison Rabenimanana, Christophe Boyaval, Sophie Eliet, Flavie Braud, Eddy Collin, Didier Theron, Xin Zhou
In this study, we present a novel platform based on scanning microwave microscopy for manipulating and detecting tiny vibrations of nanoelectromechanical resonators using a single metallic tip. The tip is placed on the top of a grounded silicon nitride membrane, acting as a movable top gate of the coupled resonator. We demonstrate its ability to map mechanical modes and investigate mechanical damping effects in a capacitive coupling scheme, based on its spatial resolution. We also manipulate the energy transfer coherently between the mode of the scanning tip and the underlying silicon nitride membrane, via parametric coupling. Typical features of optomechanics, such as anti-damping and electromechanically induced transparency, have been observed. Since the microwave optomechanical technology is fully compatible with quantum electronics and very low temperature conditions, it should provide a powerful tool for studying phonon tunnelling between two spatially separated vibrating elements, which could potentially be applied to quantum sensing.
在这项研究中,我们提出了一种基于扫描微波显微镜的新型平台,利用单个金属针尖操纵和检测纳米机电谐振器的微小振动。针尖置于接地氮化硅膜的顶部,充当耦合谐振器的可移动顶门。我们展示了其绘制机械模式图的能力,并根据其空间分辨率研究了电容耦合方案中的机械阻尼效应。我们还通过参数耦合,操纵扫描尖端模式与底层氮化硅膜之间的相干能量转移。我们观察到了光机械的典型特征,如抗阻尼和机电诱导的透明度。由于微波光机械技术与量子电子学和超低温条件完全兼容,它将为研究两个空间分离的振动元件之间的声子隧穿提供强有力的工具,并有可能应用于量子传感。
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引用次数: 0
Ion-Selective Transport Promotion Enabled by Angstrom-Scale Nanochannels in Dendrimer-Assembled Polyamide Nanofilm for Efficient Electrodialysis. 在树枝状聚合物组装的聚酰胺纳米薄膜中通过埃级纳米通道促进离子选择性传输,实现高效电渗析。
IF 9.6 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-01 DOI: 10.1021/acs.nanolett.4c01997
Baolong Wu, Ning Gan, Yuqing Lin, Yiren Zhang, Jiayu Zhang, Yulong Qiu, Xingzhong Cao, Jianguo Yu, Hideto Matsuyama

The ion permeability and selectivity of membranes are crucial in nanofluidic behavior, impacting industries ranging from traditional to advanced manufacturing. Herein, we demonstrate the engineering of ion-conductive membranes featuring angstrom-scale ion-transport channels by introducing ionic polyamidoamine (PAMAM) dendrimers for ion separation. The exterior quaternary ammonium-rich structure contributes to significant electrostatic charge exclusion due to enhanced local charge density; the interior protoplasmic channels of PAMAM dendrimer are assembled to provide additional degrees of free volume. This facilitates the monovalent ion transfer while maintaining continuity and efficient ion screening. The dendrimer-assembled hybrid membrane achieves high monovalent ion permeance of 2.81 mol m-2 h-1 (K+), reaching excellent mono/multivalent selectivity up to 20.1 (K+/Mg2+) and surpassing the permselectivities of state-of-the-art membranes. Both experimental results and simulating calculations suggest that the impressive ion selectivity arises from the significant disparity in transport energy barrier between mono/multivalent ions, induced by the "exterior-interior" synergistic effects of bifunctional membrane channels.

膜的离子渗透性和选择性在纳米流体行为中至关重要,影响着从传统工业到先进制造业的各个行业。在本文中,我们展示了通过引入离子型聚酰胺胺(PAMAM)树枝状聚合物实现离子分离的离子导电膜工程,该膜具有埃级离子传输通道。外部富含季铵的结构由于增强了局部电荷密度而产生了显著的静电电荷排斥作用;PAMAM 树枝状聚合物内部原生质通道的组装提供了额外的自由体积。这有利于单价离子转移,同时保持连续性和高效离子筛选。树枝状聚合物组装的混合膜实现了 2.81 mol m-2 h-1 (K+)的高单价离子渗透率,达到了 20.1(K+/Mg2+)的优异单价/多价选择性,超过了最先进膜的过选择性。实验结果和模拟计算都表明,这种令人印象深刻的离子选择性是由双功能膜通道的 "外部-内部 "协同效应引起的单价/多价离子间传输能垒的显著差异造成的。
{"title":"Ion-Selective Transport Promotion Enabled by Angstrom-Scale Nanochannels in Dendrimer-Assembled Polyamide Nanofilm for Efficient Electrodialysis.","authors":"Baolong Wu, Ning Gan, Yuqing Lin, Yiren Zhang, Jiayu Zhang, Yulong Qiu, Xingzhong Cao, Jianguo Yu, Hideto Matsuyama","doi":"10.1021/acs.nanolett.4c01997","DOIUrl":"https://doi.org/10.1021/acs.nanolett.4c01997","url":null,"abstract":"<p><p>The ion permeability and selectivity of membranes are crucial in nanofluidic behavior, impacting industries ranging from traditional to advanced manufacturing. Herein, we demonstrate the engineering of ion-conductive membranes featuring angstrom-scale ion-transport channels by introducing ionic polyamidoamine (PAMAM) dendrimers for ion separation. The exterior quaternary ammonium-rich structure contributes to significant electrostatic charge exclusion due to enhanced local charge density; the interior protoplasmic channels of PAMAM dendrimer are assembled to provide additional degrees of free volume. This facilitates the monovalent ion transfer while maintaining continuity and efficient ion screening. The dendrimer-assembled hybrid membrane achieves high monovalent ion permeance of 2.81 mol m<sup>-2</sup> h<sup>-1</sup> (K<sup>+</sup>), reaching excellent mono/multivalent selectivity up to 20.1 (K<sup>+</sup>/Mg<sup>2+</sup>) and surpassing the permselectivities of state-of-the-art membranes. Both experimental results and simulating calculations suggest that the impressive ion selectivity arises from the significant disparity in transport energy barrier between mono/multivalent ions, induced by the \"exterior-interior\" synergistic effects of bifunctional membrane channels.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":null,"pages":null},"PeriodicalIF":9.6,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141464384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electrically Controlled High Sensitivity Strain Modulation in MoS2 Field-Effect Transistors via a Piezoelectric Thin Film on Silicon Substrates. 通过硅基板上的压电薄膜实现 MoS2 场效应晶体管中的电控高灵敏度应变调制。
IF 9.6 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-01 DOI: 10.1021/acs.nanolett.4c00357
Abin Varghese, Adityanarayan H Pandey, Pooja Sharma, Yuefeng Yin, Nikhil V Medhekar, Saurabh Lodha

Strain can modulate bandgap and carrier mobilities in two-dimensional (2D) materials. Conventional strain-application methodologies relying on flexible/patterned/nanoindented substrates are limited by low thermal tolerance, poor tunability, and/or scalability. Here, we leverage the converse piezoelectric effect to electrically generate and control strain transfer from a piezoelectric thin film to electromechanically coupled 2D MoS2. Electrical bias polarity change across the piezo film tunes the nature of strain transferred to MoS2 from compressive (∼0.23%) to tensile (∼0.14%) as verified through Raman and photoluminescence spectroscopies and substantiated by density functional theory calculations. The device architecture, on silicon substrate, integrates an MoS2 field-effect transistor on a metal-piezoelectric-metal stack enabling strain modulation of transistor drain current (130×), on/off ratio (150×), and mobility (1.19×) with high precision, reversibility, and resolution. Large, tunable tensile (1056) and compressive (-1498) strain gauge factors, electrical strain modulation, and high thermal tolerance promise facile integration with silicon-based CMOS and micro-electromechanical systems.

应变可以调节二维(2D)材料的带隙和载流子迁移率。传统的应变应用方法依赖于柔性/图案/纳米凹痕基底,但受限于热耐受性低、可调性差和/或可扩展性差。在这里,我们利用压电效应的反向作用,从压电薄膜到机电耦合的二维 MoS2,以电气方式产生和控制应变传递。通过拉曼光谱和光致发光光谱的验证以及密度泛函理论计算的证实,压电薄膜上的电偏压极性变化可将转移到 MoS2 上的应变性质从压缩(∼0.23%)调整为拉伸(∼0.14%)。该器件结构基于硅衬底,在金属-压电-金属叠层上集成了一个 MoS2 场效应晶体管,能够以高精度、可逆性和高分辨率对晶体管漏极电流(130 倍)、导通/关断比(150 倍)和迁移率(1.19 倍)进行应变调制。可调的拉伸(1056)和压缩(-1498)应变系数大、电应变调制和高热耐受性使其可以方便地与硅基 CMOS 和微机电系统集成。
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引用次数: 0
Monoclinic LaSb2 Superconducting Thin Films. 单斜 LaSb2 超导薄膜。
IF 9.6 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-01 DOI: 10.1021/acs.nanolett.4c01068
Adrian Llanos, Giovanna Campisi, Veronica Show, Jinwoong Kim, Reiley Dorrian, Salva Salmani-Rezaie, Nicholas Kioussis, Joseph Falson

Rare-earth diantimondes exhibit coupling between structural and electronic orders, which are tunable under pressure and temperature. Here we present the discovery of a new polymorph of LaSb2 stabilized in thin films synthesized using molecular beam epitaxy. Using diffraction, electron microscopy, and first-principles calculations we identify a YbSb2-type monoclinic lattice as a yet-uncharacterized stacking configuration. The material hosts superconductivity with a Tc = 2 K, which is enhanced relative to the bulk ambient phase, and a long superconducting coherence length of 1730 Å. This result highlights the potential thin film growth has in stabilizing novel stacking configurations in quasi-two-dimensional compounds with competing layered structures.

稀土二锑呈现出结构阶和电子阶之间的耦合,这种耦合在压力和温度下是可调的。在这里,我们发现了一种新的 LaSb2 多晶体,它稳定在利用分子束外延技术合成的薄膜中。利用衍射、电子显微镜和第一原理计算,我们确定了镱锑2-型单斜晶格是一种尚未表征的堆积构型。该材料具有超导电性,Tc = 2 K,相对于体态环境相有所增强,超导相干长度为 1730 Å。这一结果凸显了薄膜生长在稳定具有竞争层状结构的准二维化合物中的新型堆积构型方面的潜力。
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引用次数: 0
Boosting Monolayer Transition Metal Dichalcogenides Growth by Hydrogen-Free Ramping during Chemical Vapor Deposition. 在化学气相沉积过程中通过无氢斜坡促进单层过渡金属二卤化物的生长。
IF 9.6 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-01 DOI: 10.1021/acs.nanolett.4c01314
Hongwei Liu, Tianyi Zhang, Peng Wu, Hae Won Lee, Zhenjing Liu, Tsz Wing Tang, Shin-Yi Tang, Ting Kang, Ji-Hoon Park, Jun Wang, Kenan Zhang, Xudong Zheng, Yu-Ren Peng, Yu-Lun Chueh, Yuan Liu, Tomás Palacios, Jing Kong, Zhengtang Luo

The controlled vapor-phase synthesis of two-dimensional (2D) transition metal dichalcogenides (TMDs) is essential for functional applications. While chemical vapor deposition (CVD) techniques have been successful for transition metal sulfides, extending these methods to selenides and tellurides often faces challenges due to uncertain roles of hydrogen (H2) in their synthesis. Using CVD growth of MoSe2 as an example, this study illustrates the role of a H2-free environment during temperature ramping in suppressing the reduction of MoO3, which promotes effective vaporization and selenization of the Mo precursor to form MoSe2 monolayers with excellent crystal quality. As-synthesized MoSe2 monolayer-based field-effect transistors show excellent carrier mobility of up to 20.9 cm2/(V·s) with an on-off ratio of 7 × 107. This approach can be extended to other TMDs, such as WSe2, MoTe2, and MoSe2/WSe2 in-plane heterostructures. Our work provides a rational and facile approach to reproducibly synthesize high-quality TMD monolayers, facilitating their translation from laboratory to manufacturing.

受控气相合成二维(2D)过渡金属二掺杂物(TMDs)对于功能性应用至关重要。虽然化学气相沉积(CVD)技术在过渡金属硫化物方面取得了成功,但由于氢气(H2)在合成中的作用不确定,将这些方法推广到硒化物和碲化物往往面临挑战。本研究以 MoSe2 的 CVD 生长为例,说明了升温过程中无 H2 环境在抑制 MoO3 还原方面的作用,从而促进 Mo 前驱体的有效汽化和硒化,形成具有优异晶体质量的 MoSe2 单层。经合成的基于 MoSe2 单层的场效应晶体管显示出卓越的载流子迁移率,高达 20.9 cm2/(V-s),导通比为 7 × 107。这种方法可扩展到其他 TMD,如 WSe2、MoTe2 和 MoSe2/WSe2 面内异质结构。我们的工作提供了一种合理而简便的方法,可重复合成高质量的 TMD 单层膜,促进其从实验室到生产的转化。
{"title":"Boosting Monolayer Transition Metal Dichalcogenides Growth by Hydrogen-Free Ramping during Chemical Vapor Deposition.","authors":"Hongwei Liu, Tianyi Zhang, Peng Wu, Hae Won Lee, Zhenjing Liu, Tsz Wing Tang, Shin-Yi Tang, Ting Kang, Ji-Hoon Park, Jun Wang, Kenan Zhang, Xudong Zheng, Yu-Ren Peng, Yu-Lun Chueh, Yuan Liu, Tomás Palacios, Jing Kong, Zhengtang Luo","doi":"10.1021/acs.nanolett.4c01314","DOIUrl":"https://doi.org/10.1021/acs.nanolett.4c01314","url":null,"abstract":"<p><p>The controlled vapor-phase synthesis of two-dimensional (2D) transition metal dichalcogenides (TMDs) is essential for functional applications. While chemical vapor deposition (CVD) techniques have been successful for transition metal sulfides, extending these methods to selenides and tellurides often faces challenges due to uncertain roles of hydrogen (H<sub>2</sub>) in their synthesis. Using CVD growth of MoSe<sub>2</sub> as an example, this study illustrates the role of a H<sub>2</sub>-free environment during temperature ramping in suppressing the reduction of MoO<sub>3</sub>, which promotes effective vaporization and selenization of the Mo precursor to form MoSe<sub>2</sub> monolayers with excellent crystal quality. As-synthesized MoSe<sub>2</sub> monolayer-based field-effect transistors show excellent carrier mobility of up to 20.9 cm<sup>2</sup>/(V·s) with an on-off ratio of 7 × 10<sup>7</sup>. This approach can be extended to other TMDs, such as WSe<sub>2</sub>, MoTe<sub>2</sub>, and MoSe<sub>2</sub>/WSe<sub>2</sub> in-plane heterostructures. Our work provides a rational and facile approach to reproducibly synthesize high-quality TMD monolayers, facilitating their translation from laboratory to manufacturing.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":null,"pages":null},"PeriodicalIF":9.6,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141464380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Solving Maxwell's Equations Using Polarimetry Alone. 仅用极坐标法求解麦克斯韦方程
IF 9.6 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-01 DOI: 10.1021/acs.nanolett.4c01976
Jorge Olmos-Trigo

Maxwell's equations are solved when the amplitude and phase of the electromagnetic field are determined at all points in space. Generally, the Stokes parameters can only capture the amplitude and polarization state of the electromagnetic field in the radiation (far) zone. Therefore, the measurement of the Stokes parameters is, in general, insufficient to solve Maxwell's equations. In this Letter, we solve Maxwell's equations for a set of objects widely used in Nanophotonics using the Stokes parameters alone. These objects are lossless, axially symmetric, and well described by a single multipolar order. Our method for solving Maxwell's equations endows the Stokes parameters an even more fundamental role in the electromagnetic scattering theory.

当确定了空间所有点的电磁场振幅和相位后,麦克斯韦方程就可以求解了。一般来说,斯托克斯参数只能捕捉辐射(远)区电磁场的振幅和极化状态。因此,测量斯托克斯参数一般不足以求解麦克斯韦方程组。在这封信中,我们仅使用斯托克斯参数求解了纳米光子学中广泛使用的一组物体的麦克斯韦方程。这些物体是无损的、轴对称的,并由单个多极阶进行了很好的描述。我们的麦克斯韦方程求解方法赋予斯托克斯参数在电磁散射理论中更重要的作用。
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引用次数: 0
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