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Janus XYTe2 monolayers and GaInTe2 bilayer: promising materials for photocatalytic water splitting - a first-principles study Janus XYTe2单层和GaInTe2双分子层:光催化水分解的有前途的材料-第一性原理研究
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-05 DOI: 10.1016/j.jsamd.2025.101065
Gang Guo , Yongcheng Chen , Gencai Guo
The quest for efficient photocatalysts for solar-driven water splitting is paramount for advancing clean hydrogen energy. Here, we systematically investigate a novel family of 2D Janus XYTe2 (X = Al, Ga; Y=Ga, In; X≠Y) monolayers and bilayer GaInTe2, using first-principles calculations. Our investigations reveal that the designed monolayers possess robust dynamic, thermal, and mechanical stability. They possess suitable band gaps (1.88–2.46 eV), high visible-light absorption coefficients, and appropriate band edge alignment for photocatalytic water splitting. Notably, GaInTe2 monolayer achieves a high solar-to-hydrogen (STH) efficiency of ∼21.5 %. More strikingly, stacking GaInTe2 into a bilayer with an AB2 configuration dramatically enhances its performance. The bilayer exhibits a reduced bandgap (1.36 eV), significantly boosted optical absorption across the visible spectrum, and achieves an ultrahigh theoretical STH efficiency of 42.21 %. Furthermore, Gibbs free energy change calculations provide evidence for the thermodynamic accessibility of the HER in these systems. The outcomes of our analysis establish the Janus XYTe2 family, with special emphasis on the AB2-stacked GaInTe2 bilayer, as an exceptional system for pioneering next-generation solar energy conversion.
为太阳能驱动的水分解寻找高效的光催化剂对于推进清洁氢能源至关重要。在这里,我们系统地研究了一类新的二维Janus XYTe2 (X = Al, Ga; Y=Ga, In; X≠Y)单层和双层GaInTe2,使用第一性原理计算。我们的研究表明,设计的单层具有强大的动态,热稳定性和机械稳定性。它们具有合适的带隙(1.88-2.46 eV)、高可见光吸收系数和适合光催化水分解的带边排列。值得注意的是,GaInTe2单层膜实现了高达21.5%的太阳能制氢(STH)效率。更引人注目的是,将GaInTe2堆叠成具有AB2结构的双层结构可以显著提高其性能。该双分子层的带隙减小了(1.36 eV),显著提高了可见光光谱的光吸收,并实现了42.21%的超高理论效率。此外,Gibbs自由能变化计算为这些体系中HER的热力学可及性提供了证据。我们的分析结果建立了Janus XYTe2家族,特别强调ab2堆叠的GaInTe2双分子层,作为开拓下一代太阳能转换的特殊系统。
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引用次数: 0
Molecular engineering of Y-series acceptors with oligo(ethylene glycol) side chains enables high efficiency in nonhalogenated solvent-processed organic solar cells 具有低聚(乙二醇)侧链的y系列受体的分子工程使非卤化溶剂处理有机太阳能电池具有高效率
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-03 DOI: 10.1016/j.jsamd.2025.101064
Kun Wang , Jia'nan Hu , Yirong Li , Cheng Zhang , Yan Gao , Kai Xiang , Longxin Li , Weijie Qin , Rui Sun , Qunping Fan , Jianhua Chen
Most high-performance organic solar cells (OSCs) based on Y6-type acceptors are fabricated using chloroform, which hinders their commercialization due to issues with film uniformity and solvent toxicity. Although high-boiling-point non-halogenated solvents are promising alternatives, they typically suffer from low solubility and slow evaporation rates, complicating the crystallization process. Herein, we introduce Y-TEG, a Y-shaped acceptor functionalized with two oligo(ethylene glycol) (OEG) side chains on the pyrrole unit of Y6, which significantly enhances its solubility in non-halogenated solvents. OSCs based on PM6:Y-TEG processed from o-xylene achieved a power conversion efficiency (PCE) of 14.22%. The incorporation of Y6 as a third component further increased the PCE to 15.77%. This improvement is attributed to the role of Y6 in modulating intermolecular compatibility, optimizing crystallinity, and enhancing the phase separation morphology of the active layer. Consequently, the exciton dissociation and charge collection efficiency are improved, while charge recombination and energy losses are reduced. Notably, the PCE of 15.77% ranks among the highest reported for devices incorporating a host acceptor modified with OEG side chain and processed using non-halogenated solvents. These results demonstrate that side-chain engineering with OEG groups is a promising strategy for developing high-efficiency photovoltaic materials compatible with environmentally friendly processing solvents, providing confidence for future large-scale device fabrication.
大多数基于y6型受体的高性能有机太阳能电池(OSCs)都是使用氯仿制造的,由于薄膜均匀性和溶剂毒性问题,这阻碍了它们的商业化。虽然高沸点非卤化溶剂是很有前途的替代品,但它们通常存在溶解度低和蒸发速度慢的问题,使结晶过程复杂化。在此,我们引入了Y-TEG,一个y形受体,在Y6的吡咯单元上被两个低聚乙二醇(OEG)侧链功能化,显著提高了其在非卤化溶剂中的溶解度。由邻二甲苯加工而成的基于PM6:Y-TEG的osc的功率转换效率(PCE)达到14.22%。Y6作为第三个组成部分的合并进一步将PCE提高到15.77%。这种改进归因于Y6在调节分子间相容性,优化结晶度和增强活性层的相分离形态方面的作用。从而提高激子解离和电荷收集效率,同时减少电荷复合和能量损失。值得注意的是,15.77%的PCE是采用OEG侧链修饰的宿主受体并使用非卤化溶剂处理的器件中最高的。这些结果表明,OEG组侧链工程是开发与环保加工溶剂兼容的高效光伏材料的有前途的策略,为未来的大规模器件制造提供了信心。
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引用次数: 0
Metal Organic Framework based Humidity Sensing: Stability, performance, and IoT Integration 基于金属有机框架的湿度传感:稳定性、性能和物联网集成
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1016/j.jsamd.2025.100972
Waseem Akram , Shahzad Iqbal , Zahir Abbas , Shiekh Mansoor , Imran Shah , Asad Ullah , Wei Xu , Woo Young Kim
The incorporation of IoT technology with advanced sensing materials is converting smart agriculture by allowing precise control over environmental conditions and optimizing resource utilization for advanced agricultural productivity. This study examines the potential of metal-organic frameworks (MOFs) for soil moisture detection in plants, focusing on their application in IoT-enabled smart agriculture systems. Two MOFs, synthesized with nickel acetate and zinc acetate, were evaluated for their humidity-sensing capabilities. The nickel acetate-based MOF had a highly porous, rod-shaped morphology with homogeneous dendrites and high capacitance, in contrast to the Zn-MOF, which exhibited clustering and reduced effective humidity collecting sites, as confirmed by Raman and XRD investigations and SEM images. Ni-MOF outperformed Zn-MOF with a 7.5 times increase in capacitance between 10 % and 90 % relative humidity and a minimal hysteresis of 3.5 % at 70 % relative humidity. Additionally, Ni-MOF demonstrated exceptional response and recovery times of 1.6 s and 0.3 s, respectively. These attributes underscore Ni-MOF's suitability for reliable and efficient soil moisture sensing in agricultural applications. By integrating Ni-MOF sensors into wireless sensor networks and IoT frameworks, this research highlights their potential to fuse field-based sensor data with proximal sensing platforms, contributing to enhanced decision-making and optimization of agricultural operations.
物联网技术与先进传感材料的结合,通过精确控制环境条件和优化资源利用来实现先进农业生产力,正在转变智能农业。本研究探讨了金属有机框架(MOFs)在植物土壤湿度检测中的潜力,重点关注它们在支持物联网的智能农业系统中的应用。用乙酸镍和乙酸锌合成了两种MOFs,并对其湿度传感能力进行了评价。Raman、XRD和SEM图像证实,醋酸镍基MOF具有高孔隙、枝晶均匀、高电容的棒状结构,而Zn-MOF则具有簇状结构和减少的有效湿度收集位点。在10% ~ 90%的相对湿度下,Ni-MOF的电容增加了7.5倍,在70%的相对湿度下,Ni-MOF的最小迟滞率为3.5%。此外,Ni-MOF的响应时间和恢复时间分别为1.6 s和0.3 s。这些特性强调了Ni-MOF在农业应用中可靠和有效的土壤水分传感的适用性。通过将Ni-MOF传感器集成到无线传感器网络和物联网框架中,本研究突出了它们将基于现场的传感器数据与近端传感平台融合在一起的潜力,有助于增强农业运营的决策和优化。
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引用次数: 0
Controlling activation parameters in phytagel-derived activated carbons for enhanced supercapacitor performance 控制植酸衍生活性炭的活化参数以增强超级电容器的性能
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1016/j.jsamd.2025.101055
Sushant Kumar , R.C. Singh , Vinay Deep Punetha , Pawan Singh Dhapola , Markus Diantoro , Manoj K. Singh , Pramod K. Singh
Activated carbons, due to their high surface area and well-developed pore structure, are excellent electrode materials for energy storage devices. The properties of activated carbons can be tuned by modifying certain factors, such as activating agent, activation temperature, time, concentration of activating agent, etc. In the present work, the effect of activating agent concentration on the properties of activated carbon is systematically investigated by synthesizing a series of samples via chemical activation and carbonization of the biopolymer, phytagel, using zinc chloride (ZnCl2) as the activating agent. Five different samples of activated carbons are prepared by using the phytagel to ZnCl2 w/w ratio in 1:0, 1:1, 1:2, 1:3, and 1:4. The prepared activated carbons are characterized using different characterization tools such as XRD, Raman, BET, SEM, TEM, EDX, XPS, etc. To study the practical application, all the activated carbons are used to fabricate solid-state supercapacitors, which are further characterized using EIS, CV, and GCD in a two-electrode geometry. The activated carbon with phytagel to ZnCl2 w/w ratio 1:3 shows the highest specific capacitance of 129 F g−1 at 0.5 A g−1 and an energy density of 17.9 Wh kg−1 at a power density of 974 W kg−1.
活性炭由于其高的比表面积和发达的孔隙结构,是一种极好的储能电极材料。通过改变活化剂、活化温度、活化时间、活化剂浓度等因素,可以调节活性炭的性能。本文以氯化锌(ZnCl2)为活化剂,通过化学活化和炭化法制备了一系列样品,系统研究了活化剂浓度对活性炭性能的影响。采用植酸与ZnCl2的w/w比为1:0、1:1、1:2、1:3和1:4制备了5种不同的活性炭样品。采用XRD、Raman、BET、SEM、TEM、EDX、XPS等表征手段对制备的活性炭进行了表征。为了研究实际应用,将所有活性炭用于制造固态超级电容器,并在双电极几何结构中使用EIS, CV和GCD进一步表征。当叶绿素与ZnCl2 w/w比为1:3时,活性炭在0.5 A g−1时的比电容最高为129 F g−1,在功率密度为974 w kg−1时的能量密度最高为17.9 Wh kg−1。
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引用次数: 0
Enhanced photocatalytic degradation of antibiotics and dye using flower-like BiOBrxI1-x solid solutions formed from self-assembled nanosheets 使用自组装纳米片形成的花状bibrxi1 -x固溶体增强抗生素和染料的光催化降解
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1016/j.jsamd.2025.101051
Shulan Pu , Dongying Wang , Xi Luo , Yuhong Ding , Jianglong Guo , Yaxiong Li , Jin Zhong Zhang , Yan Sun
Flower-like BiOBrxI1-x solid solutions with varying Br/I ratios were successfully prepared via a facile precipitation method. The photocatalytic performance was evaluated by degrading representative pollutants, including tetracycline (TC), oxytetracycline (OTC), and rhodamine B dye (RhB). All solid solutions exhibited enhanced activity compared to pure BiOBr and BiOI, and BiOBr0.5I0.5 demonstrated the highest degradation efficiencies of 81.7 %, 76.4 %, and 98.5 % for TC, OTC, and RhB within 30 min, respectively. The formation of a solid solution altered the band structure and provided multiple active sites for photocatalytic reaction, thus accelerating the separation of charge carriers. Moreover, the main active species were revealed through capture experiments and electron spin resonance tests.
通过易沉淀法成功制备了不同Br/I比的花状bibrxi1 -x固溶体。通过降解代表性污染物四环素(TC)、土霉素(OTC)和罗丹明B染料(RhB)来评价其光催化性能。与纯BiOBr和BiOI相比,所有固溶体都表现出增强的活性,其中BiOBr0.5I0.5在30 min内对TC、OTC和RhB的降解效率最高,分别为81.7%、76.4%和98.5%。固溶体的形成改变了能带结构,为光催化反应提供了多个活性位点,从而加速了载流子的分离。通过俘获实验和电子自旋共振实验,揭示了主要的活性物质。
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引用次数: 0
A novel Z-scheme CoWO4/RGO/g-C3N4 photocatalyst for efficient visible-light-induced removal of organic pollutants 新型z型CoWO4/RGO/g-C3N4光催化剂在可见光诱导下去除有机污染物
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1016/j.jsamd.2025.101056
Dang Van Do , Hung Van Tran , Giang Dac Truong Nguyen , Long Van Dang , Son Thanh Le , Khai Manh Nguyen , Trang Thu Hoang , Phuong Minh Nguyen
A ternary CoWO4/RGO/g-C3N4 photocatalyst was synthesized via a facile hydrothermal method for visible-light-driven degradation of the azo dye Direct Blue 71 (DB 71). Structural, morphological, and optical characterizations (XRD, FT-IR, SEM, EDS, UV–Vis DRS, and PL) confirmed the uniform incorporation of CoWO4 and reduced graphene oxide (RGO) into the g-C3N4 framework, resulting in enhanced visible-light absorption and suppressed charge recombination through an RGO-mediated Type-II heterojunction. The optimized 0.1CoWO4/RGO/g-C3N4 composite achieved 97 % degradation and 73 % TOC removal within 40 min, following pseudo-first-order kinetics (k = 0.08546 min-1). Behnajady–Modirshahla–Ghanbary (BMG) modeling yielded b = 0.79875 min-1 and m = 1.265, confirming high oxidative capacity. Photocatalytic activity was optimal at acidic to neutral pH and moderate catalyst dosage, with •OH and h+ identified as the dominant reactive species. The catalyst maintained 89 % efficiency after six cycles and achieved 54–74 % TOC removal in real urban surface waters from Hanoi. A preliminary techno-economic analysis estimated a production cost of 15–40 USD·kg-1, underscoring its scalability and economic viability for sustainable wastewater treatment.
采用水热法合成了CoWO4/RGO/g-C3N4三元光催化剂,用于可见光降解偶氮染料直蓝71 (DB 71)。结构、形态和光学表征(XRD、FT-IR、SEM、EDS、UV-Vis DRS和PL)证实了CoWO4和还原氧化石墨烯(RGO)在g-C3N4框架中的均匀掺入,通过RGO介导的ii型异质结增强了可见光吸收,抑制了电荷重组。优化后的0.1CoWO4/RGO/g-C3N4复合材料在40 min内达到97%的降解率和73%的TOC去除率,符合准一级动力学(k = 0.08546 min-1)。Behnajady-Modirshahla-Ghanbary (BMG)模型得出b = 0.79875 min-1, m = 1.265,证实氧化能力高。在酸性至中性pH和催化剂用量适中的条件下,光催化活性最佳,其中•OH和h+为优势反应物质。经过6次循环后,催化剂的效率保持在89%,在河内市实际城市地表水中TOC去除率达到54 - 74%。初步的技术经济分析估计生产成本为15-40美元·kg-1,强调了其可扩展性和可持续废水处理的经济可行性。
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引用次数: 0
Advances in thermoelectronic materials and devices for self-sustaining wearable and IoT systems 用于自我维持可穿戴和物联网系统的热电子材料和器件的进展
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1016/j.jsamd.2025.101059
Beemkumar Nagappan , K. Kamakshi Priya , Kulmani Mehar , Praveen Priyaranjan Nayak , Shailesh Kumar , Mahit Jain , A. Shwetha , Aseel Samrat
Thermoelectric devices that facilitate the conversion of low-grade thermal gradients into electrical energy are increasingly recognized as essential elements for self-sustaining wearable electronics and autonomous Internet of Things (IoT) infrastructures. This review provides a comprehensive evaluation of recent advancements in thermoelectric materials, flexible device architectures, and system-level power management methodologies that have been documented over the past five years. Principal areas of emphasis encompass nanostructuring, band engineering, and defect modulation strategies that augment the thermoelectric figure of merit (ZT) and power factor under low-ΔT conditions. Innovations in conducting polymers, hybrid nanocomposites, and low-dimensional materials are underscored for their mechanical flexibility, stretchability, and compatibility with scalable processing techniques. Comparative assessments of benchmark materials, including Bi2Te3 alloys, SnSe, Poly(3,4-ethylenedioxythiophene) (PEDOT): poly(styrenesulfonate) (PSS), and Carbon nanotube (CNT)/polymer composites, are presented with direct correlations to device-level performance metrics relevant to wearable applications and distributed sensor networks. In addition to summarizing advancements, this review emphasizes that successful commercialization will depend on the coordinated optimization of high-ZT, low-toxicity materials, robust architectures, and ultra-low-power electronic systems. Challenges such as scalable synthesis, long-term thermomechanical reliability, and sustainable recycling practices are critically scrutinized. Furthermore, the review aligns prospective research trajectories with Sustainable and Affordable and Clean Energy by promoting battery-free, environmentally sustainable wearable and IoT technologies.
促进低品位热梯度转化为电能的热电器件越来越被认为是自我维持的可穿戴电子产品和自主物联网(IoT)基础设施的基本要素。这篇综述全面评估了过去五年来在热电材料、柔性器件架构和系统级电源管理方法方面的最新进展。主要的重点领域包括纳米结构、能带工程和缺陷调制策略,这些策略可以在低-ΔT条件下增加热电性能图(ZT)和功率因数。导电聚合物、杂化纳米复合材料和低维材料的创新因其机械灵活性、可拉伸性和与可扩展加工技术的兼容性而得到强调。基准材料的对比评估,包括Bi2Te3合金、SnSe、聚(3,4-乙烯二氧噻吩)(PEDOT):聚(苯乙烯磺酸盐)(PSS)和碳纳米管(CNT)/聚合物复合材料,与可穿戴应用和分布式传感器网络相关的设备级性能指标直接相关。除了总结进展之外,这篇综述还强调,成功的商业化将取决于高zt、低毒性材料、坚固的结构和超低功耗电子系统的协调优化。挑战,如可扩展的合成,长期的热机械可靠性,和可持续的回收实践严格审查。此外,通过推广无电池、环境可持续的可穿戴设备和物联网技术,该综述将前瞻性研究轨迹与可持续、负担得起和清洁能源相结合。
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引用次数: 0
Optical and structural characteristics of La2O3-ZnO nanoparticles synthesized via the Co-precipitation technique: Potential for energy storage and biomedical applications 通过共沉淀法合成的La2O3-ZnO纳米粒子的光学和结构特性:储能和生物医学应用的潜力
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1016/j.jsamd.2025.101061
Manal A. Awad , Awatif A. Hendi , Khalid M. Ortashi , Saad G. Alshammari , Hayat Althobaiti , Gul Naz , Fatimah Al-Abbas , Reema A. Alnamlah , Meshal Marzoog Al-Sharafa , Raghad M. Alsubaie , Nada M. Merghani , R. Ramadan , H.J. Elamin , Fahd Z. Eissa , Eram Eltahir , Maha M. Almoneef
This study reports the synthesis of a composite of lanthanum (La2O3)–zinc oxide nanoparticles (La-ZnONPs) using a simple and cost-effective co-precipitation method. The structural, morphological, compositional, and functional properties of the synthesized nanoparticles were systematically investigated. UV–visible spectroscopy revealed an excitonic absorption peak at ∼364 nm, and the optical band gap was calculated to be 2.9 ± 0.02 eV using the Kubelka–Munk method. Fourier-transform infrared (FTIR) spectroscopy indicated the vibrational modes of functional groups, with a prominent peak in the range of 3000–3600 cm−1 corresponding to the O–H bond, while the absence of additional significant absorption bands confirmed the high purity of the nanoparticles. Transmission electron microscopy (TEM) revealed their morphology, and energy-dispersive X-ray spectroscopy (EDX) confirmed the elemental composition. X-ray diffraction (XRD) analysis showed a hexagonal wurtzite structure with an average crystallite size of ∼15 ± 0.01 nm. Electrochemical characterization demonstrated that La-ZnO electrodes exhibited a specific capacitance (Cp) of 0.8064 ± 0.001 F/g at a scan rate of 0.01 V/s, which decreased to 0.3758 ± 0.01 F/g at higher scan rates due to reduced interaction time between the active material and electrolyte ions. The observed pseudocapacitive behavior was attributed to oxygen vacancies and La incorporation, which enhanced the overall capacitance. The anticancer potential of La-ZnONPs was evaluated against colon cancer, MDA-MB-231 breast cancer, and HeLa cervical cancer cell lines using the MTT assay. The nanoparticles exhibited significant cytotoxicity, with cell viabilities of 28.5 ± 0.12 %, 25 ± 0.15 %, and 30.2 ± 0.14 % for colon, MDA-MB-231, and HeLa cells, respectively, demonstrating effective cytotoxicity at relatively low concentrations and highlighting their potential as anticancer agents. Unlike previous studies on La-ZnO, which primarily focused on structural and optical properties, this work demonstrates the dual functionality of La-ZnONPs by systematically assessing both their electrochemical and anticancer activities. These findings underscore their biomedical relevance and potential application in energy storage, offering a unique combination of multifunctional properties for future technological and therapeutic developments.
本研究报道了一种简单而经济的共沉淀法合成了镧(La2O3) -氧化锌纳米颗粒(La-ZnONPs)的复合材料。系统地研究了合成的纳米颗粒的结构、形态、组成和功能特性。紫外可见光谱在~ 364 nm处发现激子吸收峰,利用Kubelka-Munk方法计算出光学带隙为2.9±0.02 eV。傅里叶变换红外光谱(FTIR)显示了官能团的振动模式,在3000-3600 cm−1范围内有一个明显的峰对应于O-H键,而没有额外的显著吸收带证实了纳米颗粒的高纯度。透射电子显微镜(TEM)显示了它们的形态,能量色散x射线光谱(EDX)证实了它们的元素组成。x射线衍射(XRD)分析显示为六方纤锌矿结构,平均晶粒尺寸为~ 15±0.01 nm。电化学表征表明,在扫描速率为0.01 V/s时,La-ZnO电极的比电容(Cp)为0.8064±0.001 F/g,而在高扫描速率下,由于活性材料与电解质离子之间的相互作用时间减少,比电容(Cp)降至0.3758±0.01 F/g。观察到的赝电容行为归因于氧空位和La的掺入,这增强了整体电容。采用MTT法评估了La-ZnONPs对结肠癌、MDA-MB-231乳腺癌和HeLa宫颈癌细胞系的抗癌潜力。这些纳米颗粒对结肠癌、MDA-MB-231和HeLa细胞的细胞存活率分别为28.5±0.12%、25±0.15%和30.2±0.14%,显示出在相对低浓度下有效的细胞毒性,并突出了它们作为抗癌药物的潜力。与以往对La-ZnO的研究主要集中在结构和光学性质上不同,这项工作通过系统地评估其电化学和抗癌活性来证明La-ZnONPs的双重功能。这些发现强调了它们在生物医学上的相关性和在能量存储方面的潜在应用,为未来的技术和治疗发展提供了独特的多功能特性组合。
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引用次数: 0
Quatrefoil-loop metamaterial absorber with polarization-independent and wide angular stable response for dual-band explosive gas sensing 双波段爆炸气体传感中具有偏振无关宽角稳定响应的四翼环超材料吸收体
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1016/j.jsamd.2025.101067
Nadia Reza , Mohammad Rashed Iqbal Faruque , K.S. Al-mugren
A quatrefoil-loop-shaped metamaterial is designed in this paper to detect explosive gases in the C and X bands. It achieves three resonance frequencies at 6.5 GHz, 7.58 GHz, and 8.7 GHz with absorption rates of 99.9 %, 93.2 %, and 96.5 %, respectively. The absorber shows the same absorption at different polarization angles from 0° to 90° in both transverse electric (TE) and transverse magnetic (TM) modes. The absorber can sense explosive gases such as propane and butane. The sensitivity of the propane and butane is 0.47 GHz/RIU and 0.5 GHz/RIU with a quality factor of 130 and 216, respectively. The Figure of Merit values are 10 for propane and 16.67 for butane. The sensing occurs based on the refractive index. The design is based on a cost-effective FR-4 (lossy) dielectric substrate. The unit cell dimensions are 8 × 8 × 1.6 mm3. Analysis of surface current, electric fields, and magnetic fields confirms strong resonance at each band. Additionally, the design's equivalent circuit is modeled and validated in Advanced Design System (ADS). The fabricated design is measured, and the measurement results agree well with the simulated response.
本文设计了一种四翼环形超材料,用于探测C和X波段的爆炸性气体。实现了6.5 GHz、7.58 GHz和8.7 GHz三个谐振频率,吸收率分别为99.9%、93.2%和96.5%。在横向电(TE)和横向磁(TM)模式下,在0°~ 90°的不同极化角范围内,吸收体均具有相同的吸收特性。吸收器可以感应爆炸性气体,如丙烷和丁烷。丙烷和丁烷的灵敏度分别为0.47 GHz/RIU和0.5 GHz/RIU,质量因子分别为130和216。丙烷的优值为10,丁烷为16.67。感应是基于折射率进行的。该设计基于具有成本效益的FR-4(有损)介电基片。单胞尺寸为8 × 8 × 1.6 mm3。对表面电流、电场和磁场的分析证实了每个波段的强共振。此外,设计的等效电路在高级设计系统(ADS)中进行了建模和验证。对设计方案进行了测试,测试结果与仿真结果吻合较好。
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引用次数: 0
Superior enhancement in microwave absorption performance of NiFe nanowires inlaid with ZnS Nanocrystals: Synergistic effect of exchange resonance and dielectric polarization relaxation ZnS纳米晶镶嵌NiFe纳米线对微波吸收性能的显著增强:交换共振和介电极化弛豫的协同效应
IF 6.8 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1016/j.jsamd.2025.101058
Xu-Xiang Cai , Sheng-Jung Tsou , Chung-Kwei Lin , Ruey-Bin Yang , Wen-An Chiou , Hong-Ming Lin , Yuh-Jing Chiou
Lightweight radar absorbing materials (RAMs) play a crucial role in various applications requiring the absorption of electromagnetic radiation. Both large reflection loss and wide effective absorption bandwidth are key issues for RAMs. In the present study, facile and mass producible NiFe nanowires were prepared and inlaid with ZnS nanocrystals (5, 10, and 15 wt%) to improve their microwave absorption properties. The physical materials characteristics of the so-obtained ZnS/NiFe nanowires were examined using X-ray diffraction, scanning and transmission electron microscopy, and electron spectroscopy for chemical analysis, etc. Microwave absorber composites were prepared using 5 wt% optimal ZnS/NiFe nanowires and investigated to reveal their corresponding microwave absorption performance. The experimental results showed that (ZnS)10/(Ni1Fe99)90 (i.e., Ni1Fe99 NWs inlaid with 10 wt% ZnS nanocrystals) exhibited significant improvements in both microwave absorption characteristics (complex permeability and permittivity) and performance (reflection loss and effective absorption bandwidth, EAB). The minimum reflection loss was −50.32 dB at 17.60 GHz for a thickness of 1.5 mm, whereas EAB reached 7.59 GHz, ranging from 10.41 to 18.00 GHz for a 1.7 mm thickness. The superior enhancement in microwave absorption performance can be attributed to the synergistic effect of exchange resonance and dielectric polarization relaxation loss induced by the inlay of ZnS nanocrystals on Ni1Fe99 NWs.
轻型雷达吸波材料在各种需要吸收电磁辐射的应用中发挥着至关重要的作用。大的反射损耗和宽的有效吸收带宽是ram的关键问题。在本研究中,制备了易于批量生产的NiFe纳米线,并镶嵌了ZnS纳米晶体(5%,10%和15% wt%),以提高其微波吸收性能。采用x射线衍射、扫描电镜和透射电镜、电子能谱等方法对制备的ZnS/NiFe纳米线的物理材料特性进行了表征。采用5 wt%的ZnS/NiFe纳米线制备微波吸收复合材料,并对其微波吸收性能进行了研究。实验结果表明,(ZnS)10/(Ni1Fe99)90(即Ni1Fe99 NWs镶嵌10 wt% ZnS纳米晶体)在微波吸收特性(复磁导率和介电常数)和性能(反射损耗和有效吸收带宽,EAB)方面均有显著改善。当厚度为1.5 mm时,在17.60 GHz处反射损耗最小为−50.32 dB,而当厚度为1.7 mm时,反射损耗达到7.59 GHz,在10.41 ~ 18.00 GHz之间。在Ni1Fe99 NWs上嵌体ZnS纳米晶所引起的交换共振和介电极化弛豫损失的协同作用,使微波吸收性能得到了显著提高。
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Journal of Science: Advanced Materials and Devices
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