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Two-dimensional layered metal oxides (2D LMOs) for next-generation electronic devices 用于下一代电子器件的二维层状金属氧化物(2D LMOs)。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-10 DOI: 10.1039/D5NA00895F
Arpit Verma, Alka Rani and Bal Chandra Yadav

Two-dimensional layered metal oxides (2D LMOs) have emerged as a rapidly growing class of materials that combine the advantages of reduced dimensionality with the functional diversity of transition metal oxides. Their high surface-to-volume ratio, structural anisotropy, tunable bandgap, and variable oxidation states endow them with unique electrical, optical, and catalytic properties. Recent advances in atomic layer deposition, vapor-phase synthesis, and liquid-phase exfoliation have enabled the scalable fabrication of high-quality 2D LMOs with controlled stoichiometry and thickness. This review provides a comprehensive overview of their structure–property relationships, charge transport mechanisms, and interfacial phenomena, emphasizing how defect engineering, quantum confinement, and interlayer coupling can be exploited to tailor their performance. The integration of 2D LMOs into van der Waals heterostructures further enhances band alignment, charge transfer, and excitonic control, unlocking new opportunities for transistors, sensors, and spintronic and optoelectronic devices. Current challenges such as environmental stability, phase control, and large-scale processability are critically assessed. Finally, emerging computational and machine learning-guided approaches are discussed as pathways to accelerate the rational design of 2D LMOs for flexible, energy-efficient, and multifunctional electronic applications.

二维层状金属氧化物(2D LMOs)是一类快速发展的材料,它结合了降维的优点和过渡金属氧化物的功能多样性。它们的高表面体积比、结构各向异性、可调带隙和可变氧化态赋予了它们独特的电学、光学和催化性能。原子层沉积、气相合成和液相剥离的最新进展使得高质量的二维LMOs的可扩展制造具有可控的化学计量和厚度。本文综述了它们的结构-性质关系、电荷传输机制和界面现象,强调了如何利用缺陷工程、量子限制和层间耦合来调整它们的性能。将二维LMOs集成到范德华异质结构中,进一步增强了能带排列、电荷转移和激子控制,为晶体管、传感器、自旋电子和光电子器件带来了新的机遇。当前的挑战,如环境稳定性,相控制和大规模可加工性进行了严格的评估。最后,讨论了新兴的计算和机器学习指导方法,作为加速二维LMOs合理设计的途径,以实现灵活、节能和多功能的电子应用。
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引用次数: 0
Targeting brain tumours with precision: advances in magnetic nanoparticle therapy 精确靶向脑肿瘤:磁性纳米粒子治疗的进展。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-09 DOI: 10.1039/D5NA01046B
Subham Preetam, Muhammad Fazle Rabbee, Richa Mishra, Shailendra Thapliyal, Ravi Deshwal, Sarvesh Rustagi, Archana Dashmana, Rasiravathanahalli K. Govindarajan and Sumira Malik

Brain cancer remains one of the most challenging malignancies due to the blood–brain barrier (BBB), limited drug penetration, and resistance to conventional therapies. Recent advancements in magnetic nanoparticles (MNPs) have opened new avenues for targeted and efficient brain cancer treatment. MNPs offer multifunctionality, including magnetic hyperthermia therapy, targeted drug delivery, and enhanced imaging via magnetic resonance imaging (MRI). This review explores the latest progress in MNP-based theranostics, highlighting their physicochemical properties, functionalization strategies, and mechanisms of action in brain cancer therapy. Additionally, we discuss novel approaches such as stimuli-responsive nanocarriers, BBB penetration techniques, and multifunctional hybrid nanoparticles. Furthermore, preclinical and clinical studies are reviewed to assess the current status and translational challenges. Despite promising outcomes, toxicity, biodistribution, and long-term biocompatibility remain key hurdles in clinical applications. Addressing these limitations will pave the way for personalized nanomedicine-based brain cancer treatment, optimizing therapeutic efficacy and patient outcomes.

脑癌仍然是最具挑战性的恶性肿瘤之一,由于血脑屏障(BBB),有限的药物渗透,以及对传统疗法的耐药性。磁性纳米颗粒(MNPs)的最新进展为靶向和有效的脑癌治疗开辟了新的途径。MNPs具有多种功能,包括磁热疗、靶向药物输送和通过磁共振成像(MRI)增强成像。本文综述了以mnp为基础的治疗学的最新进展,重点介绍了mnp在脑癌治疗中的理化性质、功能化策略和作用机制。此外,我们还讨论了刺激响应纳米载体、血脑屏障渗透技术和多功能杂交纳米颗粒等新方法。此外,对临床前和临床研究进行了回顾,以评估其现状和转化挑战。尽管有很好的结果,毒性、生物分布和长期生物相容性仍然是临床应用的主要障碍。解决这些限制将为个性化的基于纳米医学的脑癌治疗铺平道路,优化治疗效果和患者预后。
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引用次数: 0
Broadband light absorption in cadmium telluride thin-film solar cells via composite light trapping techniques 基于复合光捕获技术的碲化镉薄膜太阳能电池宽带光吸收。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-09 DOI: 10.1039/D5NA00325C
Asif Al Suny, Tazrian Noor, Md. Hasibul Hossain, A. F. M. Afnan Uzzaman Sheikh and Mustafa Habib Chowdhury

Composite light-trapping structures offer a promising approach to achieving broadband absorption and high efficiency in thin-film solar cells (TFSCs) in order to accelerate sustainable energy solutions. As the leading material in thin-film solar technology, cadmium telluride (CdTe) faces challenges from surface reflective losses across the solar spectrum and weak absorption in the near-infrared (NIR) range. This computational study addresses these limitations by employing a dual light trapping technique: the top surfaces of both the cadmium sulfide (CdS) and CdTe layers are tapered as nanocones (NCs), while germanium (Ge) spherical nanoparticles (NPs) are embedded within the CdTe absorber layer to enhance broadband absorption. Numerical simulations using Finite-Difference Time-Domain (FDTD) and other methods are used to optimize the parameters and configurations of both nanostructures, aiming to achieve peak optoelectronic performance. The results show that a short-circuit current density (Jsc) of 35.38 mA cm−2 and a power conversion efficiency (PCE) of 27.76% can be achieved with optimal nanocone (NC) texturing and spherical Ge NP configurations, an approximately 45% and 81% increase in Jsc and PCE, respectively. To understand the enhancement mechanisms, the study includes analyses using diffraction grating theory and Mie theory. Fabricability of these structures is also evaluated. Furthermore, an additional study on the effects of incident angle variation and polarization change demonstrates that the optimal structure is robust under practical conditions, maintaining consistent performance.

复合光捕获结构为实现薄膜太阳能电池(TFSCs)的宽带吸收和高效率提供了一种有前途的方法,以加速可持续能源解决方案的发展。作为薄膜太阳能技术的主要材料,碲化镉(CdTe)面临着横跨太阳光谱的表面反射损失和近红外(NIR)范围的弱吸收的挑战。本计算研究通过采用双光捕获技术解决了这些限制:硫化镉(CdS)和碲化镉层的顶表面都被锥形为纳米锥(nc),而锗(Ge)球形纳米颗粒(NPs)被嵌入碲化镉吸收层中,以增强宽带吸收。利用时域有限差分(FDTD)等方法进行数值模拟,优化两种纳米结构的参数和结构,以达到峰值光电性能。结果表明,优化纳米锥(NC)织构和球形Ge NP结构可实现35.38 mA cm-2的短路电流密度(jsc)和27.76%的功率转换效率(PCE), jsc和PCE分别提高了约45%和81%。为了理解增强机理,研究包括衍射光栅理论和米氏理论的分析。这些结构的可制造性也进行了评估。此外,对入射角变化和偏振变化的影响进行了研究,结果表明该优化结构在实际条件下具有较强的鲁棒性,并保持了稳定的性能。
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引用次数: 0
Sustainable wastewater treatment using novel zeolite–polymer (ZePol) composite materials 新型沸石聚合物(ZePol)复合材料的可持续废水处理。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-08 DOI: 10.1039/D5NA00996K
Tasmina Khandaker, Ahmed B. M. Ibrahim, Wael S. Al-Rashed, Khalid I. Anojaidi, Waleed A. Al-Suwaylih, Mohammed A. Al-Suwaylih, Mohamed A. Habib and Muhammad Sarwar Hossain

The emergence of effective, durable waste water treatment technology is of paramount importance due to the rising threat of toxic heavy metal pollution of water resources to human health as well as the environment. In order to improve multi-functional adsorption, we present the synthesis and performance of ZePol-4, a novel zeolite–polymer composite made from ETS-4 zeolite, chitosan, polyvinyl alcohol (PVA), and L-cysteine. The crystallinity, porosity, and functional group integrity of the composite were validated by structural and morphological characterization (XRD, SEM, and EDS). Excellent uptake capacities for important heavy metals were shown by batch adsorption experiments, with equilibrium adsorption capacities of 243.5 mg g−1 (Pb2+), 170.1 mg g−1 (Hg2+), 113.5 mg g−1 (Cu2+), 80.3 mg g−1 (Cd2+), and 45.3 mg g−1 (As3+). In accordance with this, ZePol-4 achieved high removal efficiencies in 60 minutes of 98% for Pb2+, 93% for Cd2+, 88% for Hg2+, 75% for As3+, and 70% for Cu2+. The composite required less extensive chemical adjustment because it worked well over a broad pH range, with optimal removal taking place close to neutral pH. The accuracy of the removal data was guaranteed by dual quantification using UV-vis and ICP-MS. Strong binding interactions and quick kinetics were made possible by the complementary contributions of amino, hydroxyl, and thiol groups through surface complexation and ion exchange. With its quick adsorption, high selectivity, and operational compatibility with actual environmental conditions, ZePol-4 shows great promise as a scalable, environmentally friendly, and highly effective material for tertiary wastewater treatment.

由于水资源中有毒重金属污染对人类健康和环境的威胁日益严重,出现有效、持久的废水处理技术至关重要。为了提高多功能吸附性能,本文研究了以ETS-4沸石、壳聚糖、聚乙烯醇(PVA)和l-半胱氨酸为原料制备的新型沸石-聚合物复合材料ZePol-4的合成及其性能。通过结构和形态表征(XRD、SEM和EDS)验证了复合材料的结晶度、孔隙度和官能团完整性。间歇式吸附实验表明,该材料对重要重金属具有良好的吸附能力,平衡吸附量分别为243.5 mg g-1 (Pb2+)、170.1 mg g-1 (Hg2+)、113.5 mg g-1 (Cu2+)、80.3 mg g-1 (Cd2+)和45.3 mg g-1 (As3+)。在60分钟内,ZePol-4对Pb2+的去除率为98%,对Cd2+的去除率为93%,对Hg2+的去除率为88%,对As3+的去除率为75%,对Cu2+的去除率为70%。该复合材料需要较少的化学调整,因为它在很宽的pH范围内都能很好地工作,在接近中性pH的情况下进行最佳去除。通过UV-vis和ICP-MS双重定量保证了去除数据的准确性。通过表面络合和离子交换,氨基、羟基和巯基的互补作用使强结合相互作用和快速动力学成为可能。凭借其快速吸附,高选择性和与实际环境条件的操作兼容性,ZePol-4作为一种可扩展,环保,高效的三级废水处理材料具有很大的前景。
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引用次数: 0
Carbon dots as photosensitizers: unraveling their ultrafast charge transfer, challenges, and future prospects 作为光敏剂的碳点:揭示其超快电荷转移,挑战和未来前景。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-08 DOI: 10.1039/D5NA00806A
Somen Mondal

Carbon dots (C-dots) have emerged as highly promising light-harvesting materials, particularly as photosensitizers, due to their eco-friendliness, biocompatibility, and cost-efficiency. Their adaptability as photosensitizers has garnered widespread attention, marking them as pivotal materials for future technological innovations. One of the key attributes of C-dots is their dual functionality in charge transfer, enabling them to serve as both electron donors and acceptors. This charge transfer process between C-dots and small organic molecules as quenchers plays a critical role in diverse applications such as photocatalysis, sensing, and optoelectronics. In this perspective, we have discussed the capability of C-dots in confined environments, doped C-dots, C-dots/molecular hybrids, and perovskite/C-dots composites as photosensitizers. This perspective includes the origin of fluorescence and carrier dynamics in full colour light-emitting C-dots, followed by a novel way to control the photosensitizer capability of C-dots via the transfer of electrons and holes in hybrids, composites, and doped C-dots, and the effects of the core and surface in the electron transfer process. The photosensitizer capability of C-dots was investigated via exploring the charge transfer dynamics using various advanced optical techniques like steady-state and time-resolved photoluminescence and ultrafast transient absorption (TA). This perspective also focuses on understanding the ultrafast dynamics of C-dots, such as charge transfer, charge transport, and charge recombination, in various environments, composites, and hybrid systems, with an emphasis on their development as effective photosensitizers. The extensive range of reported electron donor–acceptor systems underscores the versatility of C-dots as photosensitizers, with their tuneable electronic properties tailored to address the demands of emerging technological challenges.

碳点(C-dots)因其生态友好性、生物相容性和成本效益而成为极具前景的光收集材料,特别是光敏剂。它们作为光敏剂的适应性引起了广泛的关注,标志着它们是未来技术创新的关键材料。c点的关键属性之一是其电荷转移的双重功能,使其能够同时充当电子供体和受体。这种c点与小有机分子之间的电荷转移过程作为猝灭剂在光催化、传感和光电子等多种应用中起着关键作用。从这个角度来看,我们讨论了C-dots在受限环境中的性能、掺杂C-dots、C-dots/分子杂化物以及钙钛矿/C-dots复合材料作为光敏剂的性能。这一视角包括全彩发光c点荧光和载流子动力学的起源,然后是通过杂化、复合和掺杂c点中电子和空穴的转移来控制c点光敏剂能力的新方法,以及电子转移过程中核心和表面的影响。利用稳态、时间分辨光致发光和超快瞬态吸收等先进的光学技术,研究了C-dots的电荷传递动力学,研究了C-dots的光敏剂性能。该观点还侧重于理解c点的超快动力学,如电荷转移、电荷输运和电荷重组,在各种环境、复合材料和混合系统中,重点是它们作为有效光敏剂的发展。广泛报道的电子供体-受体系统强调了c点作为光敏剂的多功能性,其可调谐的电子特性可满足新兴技术挑战的需求。
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引用次数: 0
Valley splitting and anomalous valley Hall effect in MoTe2/CrSCl heterostructure MoTe2/CrSCl异质结构中的谷分裂和异常谷霍尔效应。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-05 DOI: 10.1039/D5NA00834D
Jaehong Park, Dongchul Sung, Junho Yun and Suklyun Hong

Two-dimensional valleytronics offers a promising platform for novel information processing and quantum technologies by harnessing the valley degree of freedom. A key challenge lies in lifting valley degeneracy, for which magnetic proximity effects provide a promising route. Here, we demonstrate substantial valley splitting in a MoTe2/CrSCl heterostructure via first-principles calculations. We show that interlayer charge transfer and interfacial orbital hybridization critically govern the valley physics at the interface. Under a moderate in-plane tensile strain (3%) and an applied out-of-plane electric field (0.2 V Å−1), a sizable valley splitting of 63 meV emerges at the valence band maximum. These conditions induce hole doping and a pronounced Berry curvature of −23 Å2 at the K valley, realizing an electrically tunable anomalous valley Hall effect. Our findings establish the MoTe2/CrSCl interface as a versatile platform for valley-selective charge transport, opening pathways for valleytronic device applications.

二维谷电子学通过利用谷自由度为新型信息处理和量子技术提供了一个有前途的平台。一个关键的挑战在于提升谷简并,磁邻近效应为提升谷简并提供了一条有希望的途径。在这里,我们通过第一性原理计算证明了MoTe2/CrSCl异质结构中存在大量的谷分裂。我们发现层间电荷转移和界面轨道杂化对界面谷物理有重要的控制作用。在中等的面内拉伸应变(3%)和面外电场(0.2 V Å-1)作用下,价带最大值处出现了较大的63 meV谷裂。这些条件诱导空穴掺杂和K谷明显的-23 Å2的Berry曲率,实现了电可调谐的异常谷霍尔效应。我们的研究结果建立了MoTe2/CrSCl接口作为谷选择电荷传输的通用平台,为谷电子器件应用开辟了途径。
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引用次数: 0
Theoretical study on the multi-mechanism synergistic bactericidal effect of asymmetric Janus AuNPs–PS microspheres 非对称Janus AuNPs-PS微球多机制协同杀菌效应的理论研究。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-05 DOI: 10.1039/D5NA00955C
Lingcong He, Hongyang Xu, Yonghui Yang and Xue-Bo Chen

With the overuse of antibiotics and the emergence of increasingly complex application scenarios, single-strategy bactericidal approaches are proving increasingly inadequate in today's environment. How to simultaneously attack multiple “targets” from multiple dimensions has become one of the hot topics in current research. This study proposes a multi-mechanism synergistic antibacterial platform based on Janus polystyrene–gold nanoparticle (AuNPs–PS) microspheres using COMSOL 6.3. This platform achieves the displacement motion of Janus AuNPs–PS microspheres through the UV-induced photothermal effect (PTT), and combines dielectrophoretic force (DEP) to enable controlled enrichment and directional arrangement of the microspheres. It achieves enhanced sterilization efficiency through the synergistic interaction of the photothermal effect and DEP based on Janus AuNPs. The study first simulated the light absorption–scattering model of AuNPs–PS microspheres under UV irradiation, verifying that the microspheres can generate a temperature field via the photothermal effect. Subsequently, the motion of the microspheres under thermophoresis and their effective separation under DEP were simulated to assess their feasibility in practical applications. Finally, the paper compares the bactericidal rates achieved by the microspheres under UV irradiation alone versus under multi-mechanism synergy. Simulation results indicate that the synergistic effect of multiple mechanisms yields a bactericidal efficacy approximately 30% higher than that of a single strategy. Among these, UV itself has a bactericidal effect. Relevant literature indicates that AuNPs can generate high temperatures under the photothermal effect, thereby disrupting bacterial membrane structures to a certain extent. Furthermore, the photocatalytic effect on the AuNP surface can catalyze the production of large amounts of reactive oxygen species (ROS) under appropriate conditions, facilitating the inactivation of certain bacteria. The PS matrix serves as an ideal carrier for AuNPs, with its excellent functionalization and dielectric properties providing the foundation for DEP manipulation. Furthermore, the spatial targeting and enrichment effect of DEP significantly enhances the local microsphere concentration and contact efficiency with bacteria. This multi-synergistic approach combining “physical enrichment–photothermal–photocatalysis” offers a potential strategy for overcoming bacterial resistance barriers. Under simulated conditions, it demonstrates promising removal potential against persistent biofilms, providing a theoretical mechanism for combating drug-resistant bacterial infections without readily inducing resistance. However, this inference requires validation through biological experiments. The study aims to provide theoretical foundations and simulation guidance for developing highly efficient sterilization technologies.

随着抗生素的过度使用和越来越复杂的应用场景的出现,单一策略的杀菌方法在当今环境中越来越不适用。如何从多个维度同时攻击多个“目标”已成为当前研究的热点之一。本研究利用COMSOL 6.3构建了基于Janus聚苯乙烯-金纳米颗粒(AuNPs-PS)微球的多机制协同抗菌平台。该平台通过紫外光诱导光热效应(PTT)实现Janus AuNPs-PS微球的位移运动,并结合介电泳力(DEP)实现微球的可控富集和定向排列。以Janus AuNPs为基础,通过光热效应与DEP的协同作用,达到提高杀菌效率的目的。本研究首先模拟了紫外线照射下AuNPs-PS微球的光吸收-散射模型,验证了微球可以通过光热效应产生温度场。随后,模拟了微球在热泳下的运动和在DEP下的有效分离,以评估其在实际应用中的可行性。最后,比较了微球在单独紫外线照射和多机制协同作用下的杀菌率。仿真结果表明,多种机制的协同效应比单一策略的杀菌效果高约30%。其中,紫外线本身具有杀菌作用。相关文献表明,AuNPs在光热作用下可以产生高温,从而在一定程度上破坏细菌膜结构。此外,AuNP表面的光催化作用可以在适当条件下催化大量活性氧(ROS)的产生,促进某些细菌的灭活。PS矩阵是aunp的理想载体,其优异的功能化和介电性能为DEP的操作提供了基础。此外,DEP的空间靶向和富集效应显著提高了局部微球浓度和与细菌的接触效率。这种结合“物理富集-光热-光催化”的多协同方法为克服细菌抗性屏障提供了一种潜在的策略。在模拟条件下,它显示出对持久性生物膜的去除潜力,为抵抗耐药细菌感染提供了理论机制,而不会轻易引起耐药性。然而,这一推论需要通过生物学实验来验证。本研究旨在为开发高效灭菌技术提供理论基础和仿真指导。
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引用次数: 0
Magnetically driven, plant-extract-modified Fe3O4 nanoparticles for sustainable and eco-friendly wastewater detoxification: recent developments 磁性驱动,植物提取物修饰的Fe3O4纳米颗粒用于可持续和生态友好的废水解毒:最新进展。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-04 DOI: 10.1039/D5NA00893J
Chanchal Das and Goutam Biswas

The increasing burden of toxic heavy metals, dyes, pharmaceuticals, and pathogenic microorganisms in aquatic environments necessitates the development of sustainable purification strategies. This review comprehensively elucidates recent progress in the synthesis, characterization, and application of phytogen-based synthesis of functionalized magnetic nanoparticles (phytogen@MNPs) for eco-friendly wastewater treatment. Plant-derived bioactive compounds serve as green capping agents, facilitating the synthesis of multifunctional, biocompatible, and surface-reactive MNPs. This review details diverse phytogenic sources, synthesis methodologies, and advanced characterization techniques, highlighting the influence of surface modification on stability, adsorption efficiency, and superparamagnetic behavior. Applications in the adsorption and catalytic degradation of inorganic, organic, and microbial contaminants are critically discussed, along with the kinetics, isotherms, and thermodynamics of pollutant removal. The antibacterial properties, reusability, and impact of real water matrices are covered, highlighting the superior performance and cost-effectiveness of phytogen@MNPs. Mechanistic insights into pollutant–nanoparticle interactions reveal the decisive roles of surface functionalization and particle size. This review also encompasses the advantages of phytogen@MNPs over conventional materials, while also identifying the need for standardized protocols, evaluation of long-term stability, and strategies for scalable production to fully realize their potential in environmental remediation in future work.

水生环境中有毒重金属、染料、药物和病原微生物的负担日益增加,需要开发可持续的净化策略。本文综述了基于植物原的功能化磁性纳米颗粒的合成、表征和应用的最新进展(phytogen@MNPs)。植物源性生物活性化合物可作为绿色封盖剂,促进多功能、生物相容性和表面反应性MNPs的合成。本文详细介绍了不同的植物来源、合成方法和先进的表征技术,重点介绍了表面改性对稳定性、吸附效率和超顺磁性行为的影响。在无机、有机和微生物污染物的吸附和催化降解中的应用,以及污染物去除的动力学、等温线和热力学进行了严格的讨论。涵盖了真实水基质的抗菌性能,可重用性和影响,突出了phytogen@MNPs的优越性能和成本效益。污染物与纳米颗粒相互作用的机理揭示了表面功能化和颗粒大小的决定性作用。这篇综述还包括phytogen@MNPs相对于传统材料的优势,同时也确定了标准化方案、长期稳定性评估和可扩展生产战略的必要性,以充分发挥其在未来工作中的环境修复潜力。
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引用次数: 0
Thermoelectric and electronic transport properties of thermal and plasma-enhanced ALD grown titanium nitride thin films 热等离子体增强氮化钛薄膜的热电和电子输运特性。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-04 DOI: 10.1039/D5NA00914F
Priyanka Goel, Christoffer Kauppinen, Ramesh Raju and Ilkka Tittonen

Titanium nitride (TiN) thin films demonstrate high electrical conductivity and thermal stability up to 400 °C in ambient conditions, with stability extending to 600–800 °C under inert or vacuum environments. Unlike many metals and transition metal nitrides, TiN combines high carrier mobility with moderate carrier concentration, making it ideal for thermal management and power-efficient applications in nanoelectronics and energy harvesting. This study systematically investigates the thermoelectric and electronic transport properties of TiN films grown by plasma-enhanced atomic layer deposition (PEALD), comparing them to those produced using traditional thermal atomic layer deposition (thermal ALD). These properties are studied as a function of growth temperature and the number of growth cycles. In particular, TiN films deposited by PEALD at 400 °C for 2000 ALD cycles exhibited a remarkable power factor of 512 µW m−1 K−2 at room temperature compared to a power factor of 4.95 µW m−1 K−2 measured for thermal ALD films fabricated under the same deposition conditions. Additionally, thermal conductivity was also measured for thicker TiN films (86 nm), yielding values of 26.96 W m−1 K−1 for PEALD and 7.01 W m−1 K−1 for thermal ALD, marking the first such report for ALD-grown TiN. These values offer an upper estimate of the thermal behavior in thinner films. Based on these measured properties, the thermoelectric figure of merit (zT) at room temperature was calculated to be 0.0056 for PEALD TiN films which is significantly higher than the value of 0.0002 obtained for thermal ALD TiN films. Our findings provide critical insights into transport properties of TiN, offering guidance for the development of conductive nanolayers in thermoelectric, nanoelectronic, and on-chip cooling applications, where precise control over thermal and electronic behavior is vital, thereby expanding the relevance of ALD TiN in high-performance applications.

氮化钛(TiN)薄膜在环境条件下具有高达400°C的高导电性和热稳定性,在惰性或真空环境下稳定性可扩展到600-800°C。与许多金属和过渡金属氮化物不同,TiN结合了高载流子迁移率和适度载流子浓度,使其成为纳米电子和能量收集领域热管理和节能应用的理想选择。本研究系统地研究了等离子体增强原子层沉积(PEALD)制备的TiN薄膜的热电和电子输运特性,并将其与传统热原子层沉积(thermal atomic layer deposition, ALD)制备的TiN薄膜进行了比较。研究了这些性质与生长温度和生长循环次数的关系。特别是,在400°C下经过2000次ALD循环,PEALD沉积的TiN薄膜在室温下的功率因数为512µW m-1 K-2,而在相同沉积条件下制备的热ALD薄膜的功率因数为4.95µW m-1 K-2。此外,还测量了较厚的TiN薄膜(86 nm)的导热系数,PEALD的导热系数为26.96 W m-1 K-1,热ALD的导热系数为7.01 W m-1 K-1,这是首次报道ALD生长TiN的导热系数。这些值提供了较薄薄膜中热行为的上限估计。根据这些测量的性能,计算出PEALD TiN薄膜在室温下的热电性能值(zT)为0.0056,明显高于热ALD TiN薄膜的0.0002。我们的研究结果为TiN的输运特性提供了重要的见解,为热电、纳米电子和片上冷却应用中导电纳米层的开发提供了指导,在这些应用中,对热和电子行为的精确控制至关重要,从而扩大了ALD TiN在高性能应用中的相关性。
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引用次数: 0
Synthetic methodologies of gold nanorod@MOF nanohybrids focused on biological applications 金nanorod@MOF纳米杂化物的合成方法侧重于生物应用。
IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-03 DOI: 10.1039/D5NA00832H
Catherine E. Araneda, Aldo A. Campos, Monica Soler and Marcelo J. Kogan

A stable and controllable coating can be formed on the surface of gold nanorods (AuNRs) by using metal–organic frameworks (MOFs), which avoids the agglomeration of the nanohybrid AuNR@MOF and also expands the functionality of the plasmon nanoparticles. In this review, we discuss the chemical role of the different components of the nanohybrid, i.e., AuNR, surface ligand or mesoporous nanostructure (MN) and the MOF around the AuNR. The methodologies used in the different synthesis stages and the factors to be considered to maintain stability in the construction of this type of nanostructures are also reported. Furthermore, we observed that there are a wide variety of MOF morphologies that can be built around AuNRs, even using the same components for their formation, which vary depending on the synthesis methodology. Finally, we discuss about the broad range of applications, of the AuNR@MOF nanohybrids, mainly in the biological field.

利用金属-有机骨架(mof)在金纳米棒(aunr)表面形成稳定可控的涂层,既避免了纳米杂化物AuNR@MOF的团聚,又扩展了等离子体纳米粒子的功能。在这篇综述中,我们讨论了纳米杂化的不同组成部分,即AuNR,表面配体或介孔纳米结构(MN)以及AuNR周围的MOF的化学作用。本文还报道了在不同合成阶段使用的方法以及在构建这种类型的纳米结构时需要考虑的保持稳定性的因素。此外,我们观察到,在aunr周围可以构建各种各样的MOF形态,即使使用相同的成分来形成它们,也会根据合成方法而有所不同。最后,我们讨论了AuNR@MOF纳米杂交体的广泛应用,主要是在生物领域。
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引用次数: 0
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