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Design and characterization of novel graphene-enhanced vapor chambers for lightweight and high-performance electronics cooling. 用于轻量化和高性能电子冷却的新型石墨烯增强蒸汽室的设计和表征。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-06 DOI: 10.1088/1361-6528/ad9f6d
Markus Enmark, Murali Murugesan, Hongfeng Zhang, Torbjörn M J Nilsson, Kai J Kallio, Arian Kamal, Johan Liu

The trend towards miniaturization of electronics and increasing transistor density in semiconductors requires more efficient cooling solutions. Vapor chambers are well established passive cooling devices that are used in a wide variety of electronics. Commercial vapor chambers are often made of high-density metals such as copper which can be a downside in lightweight applications such as laptops, smartphones, and tablets. In this study, different novel lightweight graphene-enhanced vapor chambers were built using graphene-assembled film with high thermal conductivity as envelope material. The thermal performance of the designed graphene-enhanced vapor chambers was characterized in a customized test rig and compared to a copper vapor chamber. One of the graphene-enhanced vapor chambers was shown to have 21.6% lower thermal resistance than that of a copper vapor chamber with the same design. A mass-based thermal resistance parameter was introduced as a figure of merit to account for the superior low density of the graphene-enhanced vapor chambers. The mass-based thermal resistance of the graphene-enhanced vapor chamber was seen to be 46.5% lower than that of the copper vapor chamber. The result of this study shows that replacing copper with graphene-assembled film as envelope in vapor chambers can both reduce thermal resistance and decrease the mass of the device. Hence, it is believed that graphene-enhanced vapor chambers have great potential for replacing conventional metal-based vapor chambers in lightweight and high-performance electronics and power module cooling applications in the future.

电子产品小型化的趋势和半导体中晶体管密度的增加需要更有效的冷却解决方案。蒸汽室是一种成熟的被动冷却装置,广泛应用于各种电子产品中。商业蒸汽室通常由高密度金属(如铜)制成,这在笔记本电脑、智能手机和平板电脑等轻型应用中可能是一个缺点。在本研究中,使用具有高导热性的石墨烯组装膜作为包壳材料,构建了不同的新型轻质石墨烯增强蒸汽室。设计的石墨烯增强蒸汽室的热性能在一个定制的测试平台上进行了表征,并与铜蒸汽室进行了比较。其中一种石墨烯增强蒸汽室的热阻比相同设计的铜蒸汽室低21.6%。引入了一个基于质量的热阻参数,作为考虑石墨烯增强蒸汽室优越的低密度的优点。石墨烯增强蒸汽室的质量热阻比铜蒸汽室低46.5%。研究结果表明,用石墨烯组装薄膜代替铜作为蒸汽室的包壳,既可以降低热阻,又可以降低器件的质量。因此,人们相信石墨烯增强的蒸汽室在未来的轻量化和高性能电子和电源模块冷却应用中具有取代传统金属基蒸汽室的巨大潜力。
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引用次数: 0
Preparation of novel B/ZnO/zeolite nanocomposites by simple combustion method for enhanced dye removal in an aqueous environment. 用简单燃烧法制备新型B/ZnO/沸石纳米复合材料,以增强水环境下的染料去除。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-06 DOI: 10.1088/1361-6528/ada29b
Thu Huong Nguyen, Le Van Duong, Anh-Tuan Vu

In this study, the mixture of zinc acetate dehydrates and boric acid was pyrolyzed in zeolite X to prepare novel B/ZnO/zeolite nanocomposites for the enhanced removal of tartrazine (TA) in aqueous environment. The composites are porous material with a relatively large pore size (35.3 nm). The surface area of the composite (19.72 m2g-1) is smaller than that of zeolite (248.78 m2g-1), but its adsorption capacity is quite high (qmaxof 97.6 mg g-1). The factors influencing the adsorption process were investigated in detail. Under the optimal conditions (the initial dye concentration of 20 mg l-1, the adsorbent content of 0.5 g l-1, pH equal 6, and the temperature of 25°C), the removal efficiency (Re) was 97.5%. The first and second-order equations were used to model the kinetic adsorption. The Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich models were used to study isothermal adsorption. In addition, the thermodynamic of adsorption was also investigated. The ΔHoof -52.423±2.306 kJ mol-1indicates the exothermic process and the negative ΔGoindicates a spontaneous process. At low temperatures, the adsorption of TA proceeds smoother and more effectively, and the negative ΔSo(-129.638 7.376 J·mol-1·K-1) indicates a decrease in the degree of freedom of the adsorbed species. The adsorption mechanism was also proposed.

本研究将醋酸锌脱水液与硼酸的混合物在沸石X中进行热解,制备新型B/ZnO/沸石纳米复合材料,以增强水环境中酒黄石(TA)的去除效果。复合材料为多孔材料,孔径较大(35.3 nm)。复合材料的表面积(19.72 m2/g)小于沸石的表面积(248.78 m2/g),但其吸附容量相当高(qmax为89.0 mg/g)。对影响吸附过程的因素进行了详细的研究。在初始染料浓度为20 mg/L,吸附剂含量为0.5 g/L, pH = 6,温度为25℃的最佳条件下,去除率(Re)为97.5%。采用一阶和二阶方程来模拟吸附动力学。采用Langmuir、Freundlich、Temkin和Dubinin-Radushkevich模型研究等温吸附。此外,还研究了吸附的热力学性质。∆Ho为-56.219 kJ。mol-1表示放热过程,负的∆Go表示自发过程。在低温条件下,TA的吸附更平稳有效,负的∆So (-142.036 j.l l-1 - k -1)表示被吸附物质的自由度降低。并提出了吸附机理。
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引用次数: 0
Fabrication of strain-sensing fibers with silver nanoparticles and reduced graphene oxide via wet spinning. 湿纺丝法制备纳米银和还原氧化石墨烯应变传感纤维。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-06 DOI: 10.1088/1361-6528/ada2f4
Xiaoyuan Liu, Qiuyu Xu, Xuepeng Zhang, Wei Jiang, Junmei Li, Runan Pan, Ruochen Song, Lifang Liu

To advance the industrialization of flexible strain sensors, an innovative flexible sensing fiber was developed through a sophisticated wet spinning process. Silver trifluoroacetate and graphene oxide (GO) were combined with thermoplastic polyurethane (TPU) to prepare the fibers via wet spinning. Ascorbic acid was used toin situreduce the silver trifluoroacetate and graphene oxide within the polyurethane, causing the growth of silver nanoparticles to bond with reduced graphene oxide, forming a dual conductive pathway. This resulted in the creation of silver nanoparticles/reduced graphene oxide/polyurethane fibers (AgNPs-rGO-TPU sensing fibers). The tensile and sensing properties of AgNPs-rGO-TPU sensing fibers under different parameters were investigated. The results showed that with 25 wt% TPU as the matrix, 30 wt% silver trifluoroacetate, and 1 wt% graphene oxide, the fibers achieved an optimal balance of mechanical and sensing properties. The tensile strength was 7.69 MPa, the elongation at break was 370.75%, and the toughness modulus was 18.45 MJ m-3. The AgNPs-rGO-TPU sensing fibers effectively detect external stimuli, exhibiting high sensitivity over a wide strain range (gauge factor is 4.25 below 5% strain, 24.79 in the 5%-25% strain range, 23.06 in the 25%-80% strain range, and 21.32 in the 80%-110% strain range), with a conductivity of 163.17 ms·cm-1. They can stably recognize movements and physiological signals from various parts of the human body, showing good application prospects.

为推进柔性应变传感器的产业化,采用先进的湿法纺丝工艺,研制了一种新型柔性传感纤维。将三氟乙酸银(C2AgF3O2)和氧化石墨烯(GO)与热塑性聚氨酯(TPU)结合,采用湿法纺丝制备纤维。使用抗坏血酸(L-AA)原位还原聚氨酯中的三氟乙酸银和氧化石墨烯,使银纳米颗粒与还原的氧化石墨烯结合,形成双导电途径。这导致了银纳米颗粒/还原氧化石墨烯/聚氨酯纤维(AgNPs-rGO-TPU传感纤维)的产生。研究了不同参数下AgNPs-rGO-TPU传感纤维的拉伸性能和传感性能。结果表明,以25wt%的TPU为基体,30wt%的三氟乙酸银和1wt%的氧化石墨烯为基体,纤维的机械性能和传感性能达到了最佳平衡。拉伸强度为7.69 MPa,断裂伸长率为370.75%,韧性模量为18.45 MJ·m-3。AgNPs-rGO-TPU传感纤维能有效检测外界刺激,在较宽应变范围内具有较高的灵敏度(5%应变下GF为4.25,5%-25%应变范围内GF为24.79,25%-80%应变范围内GF为23.06,80%-110%应变范围内GF为21.32),电导率为163.17 ms·cm-1。它们能够稳定地识别来自人体各部位的运动和生理信号,具有良好的应用前景。
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引用次数: 0
Percolation theory-based KMC simulation for scaled Fe-FET based multi-bit computing-in-memory with temperature compensation strategy. 基于渗透理论的基于温度补偿策略的缩放Fe-FET多比特内存计算KMC仿真。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-02 DOI: 10.1088/1361-6528/ada4b8
Qingxiao Zhu, Lihua Xu, Zhidao Zhou, Wei Wei, Pan Xv, Chunmeng Dou, Lingfei Wang, Qing Luo, Ling Li

In this letter, we investigated the impact of percolation transport mechanisms on ferroelectric field effect transistor (FeFET) multi-value storage with Kinetic Monte-Carlo (KMC) simulation considering aspect ratio and temperature dependencies. It is found that the portion of the ferroelectric polarization, which dominated the threshold voltage shift of the FeFET, increases when aspect ratio of device decreases. Moreover, randomness of percolation path formation and variations of equivalent conductance can be suppressed, indicating mitigation of device-to-device variations and enhancement of separation of individual states. Besides, to further investigate an amorphous channel promising in multi-bit applications, disorder effects in channel contribute to intrinsic percolation transport, coupling with multi-domain dynamics in Fe-layer, are studied by the high temperature characterization. On this basis, the KMC scheme is further modified to predict multi-value distribution from 300 K to 400 K. To tackle with such critical reliability issues induced inaccuracy for in-memory computing (CIM), an efficient write-verify scheme is proposed to mitigate state overlapping and provides in-depth insights for co-design of device reliability and multi-bit CIM performances. .

在这封信中,我们研究了渗透输运机制对铁电场效应晶体管(FeFET)多值存储的影响,采用动力学蒙特卡罗(KMC)模拟考虑了宽高比和温度依赖性。研究发现,当器件宽高比减小时,控制ffet阈值电压位移的铁电极化部分增大。此外,渗透路径形成的随机性和等效电导的变化可以被抑制,这表明器件之间的变化得到了缓解,单个状态的分离得到了增强。此外,为了进一步研究具有多比特应用前景的非晶通道,通过高温表征研究了通道中的无序效应对铁层内禀渗透输运的影响,并耦合了铁层中的多域动力学。在此基础上,进一步改进KMC方案,预测300 ~ 400 K的多值分布。为了解决内存计算(in-memory computing, CIM)中导致不准确的关键可靠性问题,提出了一种有效的写验证方案来缓解状态重叠,并为设备可靠性和多比特CIM性能的协同设计提供了深入的见解。
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引用次数: 0
Modulating the properties of g-C3N4 through two-step annealing and ionic-liquid gating. 通过两步退火和离子-液体门控调制g-C3N4的性能。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-02 DOI: 10.1088/1361-6528/ada4b7
Na Sa, Kaiqi Nie, Yi Sheng Ng, Tielong Deng, Jinfeng Xu, Weichao Wang, Yixiao Deng, Jia-Ou Wang, Junyong Kang, Jin-Cheng Zheng, Meng Wu, Hui-Qiong Wang

We reported a novel strategy by the combination of two-step annealing treatment and ionic-liquid gating technology for effectively regulating the properties of g-C3N4, especially largely reducing the recombination rate of the electron-hole pairs, with evidenced by the remarkable reduction of photoluminescence (PL) intensity. Firstly, graphitic carbon nitrides with typical layered structure were obtained by annealing melamine with temperature above 500°C. Further annealing at 600°C with much longer time (from 2 hours to 12 hours) were found to effectively reduce the imperfections or defects, and thus the PL intensity (49% reduction). Secondly, by post-treating annealed sample with ionic liquid, the PL were found to be further reduced, mainly due to the passivation of charged defect centers by ionic liquid. Additionally, applying an external electric field in an ionic liquid (IL) environment significantly enhance charged defect passivation. The ionic liquid gating resulted in a larger bandgap and further reduced PL intensity. This study demonstrates a new approach for defect passivation, providing insights and strategies for modulating properties of advanced materials such as g-C3N4. .

我们报告了一种结合两步退火处理和离子液体门控技术的新策略,该策略可有效调节 g-C3N4 的性能,尤其是大大降低电子-空穴对的重组率,光致发光(PL)强度的显著降低就是证明。首先,将三聚氰胺在 500°C 以上的温度下退火,可以得到具有典型层状结构的石墨化碳氮化物。进一步在 600°C 高温下退火,并延长退火时间(从 2 小时到 12 小时不等),发现可有效减少缺陷或瑕疵,从而降低光致发光强度(降低 49%)。其次,用离子液体对退火后的样品进行后处理,发现聚光强度进一步降低,这主要是由于离子液体对带电缺陷中心的钝化作用。此外,在离子液体(IL)环境中施加外部电场可显著增强带电缺陷的钝化。离子液体栅极导致带隙增大,并进一步降低了聚光强度。这项研究展示了一种新的缺陷钝化方法,为调节 g-C3N4. 等先进材料的性能提供了见解和策略。
{"title":"Modulating the properties of g-C3N4 through two-step annealing and ionic-liquid gating.","authors":"Na Sa, Kaiqi Nie, Yi Sheng Ng, Tielong Deng, Jinfeng Xu, Weichao Wang, Yixiao Deng, Jia-Ou Wang, Junyong Kang, Jin-Cheng Zheng, Meng Wu, Hui-Qiong Wang","doi":"10.1088/1361-6528/ada4b7","DOIUrl":"https://doi.org/10.1088/1361-6528/ada4b7","url":null,"abstract":"<p><p>We reported a novel strategy by the combination of two-step annealing treatment and ionic-liquid gating technology for effectively regulating the properties of g-C3N4, especially largely reducing the recombination rate of the electron-hole pairs, with evidenced by the remarkable reduction of photoluminescence (PL) intensity. Firstly, graphitic carbon nitrides with typical layered structure were obtained by annealing melamine with temperature above 500°C. Further annealing at 600°C with much longer time (from 2 hours to 12 hours) were found to effectively reduce the imperfections or defects, and thus the PL intensity (49% reduction). Secondly, by post-treating annealed sample with ionic liquid, the PL were found to be further reduced, mainly due to the passivation of charged defect centers by ionic liquid. Additionally, applying an external electric field in an ionic liquid (IL) environment significantly enhance charged defect passivation. The ionic liquid gating resulted in a larger bandgap and further reduced PL intensity. This study demonstrates a new approach for defect passivation, providing insights and strategies for modulating properties of advanced materials such as g-C3N4.&#xD.</p>","PeriodicalId":19035,"journal":{"name":"Nanotechnology","volume":" ","pages":""},"PeriodicalIF":2.9,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142922256","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Elimination of antibiotic contaminants from wastewater using polycarbazole nanocomposites as microwave-activated catalysts. 用聚咔唑纳米复合材料微波催化去除废水中的抗生素污染物。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-12-30 DOI: 10.1088/1361-6528/ada1dd
Jannatun Zia, Noushi Zaidi, Sapana Jadoun, Ufana Riaz

Ciprofloxacin (CIP) is a widely used antibiotic, and its presence in water bodies poses a risk due to its resistance to conventional wastewater treatment processes. The accumulation of such pharmaceuticals can disrupt aquatic ecosystems, harm aquatic life, and contribute to ecological imbalances. Therefore, the degradation of CIP is of immense environmental significance. This study presents the microwave-assisted catalytic degradation of the antibiotic drug CIP using nanocomposites of carbazole copolymerized with pyrrole (PCz-co-PPy) and with thiophene (PCz-co-PTh). The PCz-co-PPy and PCz-co-PTh nanocomposites were synthesized through an ultrasound-assisted method. The resulting nanocomposites were characterized using spectral and morphological analyses. FT-IR and UV-Vis spectroscopy confirmed successful intercalation and copolymerization, while FESEM images revealed a chain-like morphology. These copolymer nanocomposites were employed as microwave-active catalysts for CIP degradation, achieving an optimal degradation efficiency of 95% within 21 min using PCz-co-PPy-50/50 and PCz-co-PTh-50/50 at 600 W microwave power. The degradation followed pseudo-first-order kinetics, with rate constants calculated as 0.031 min-1, 0.020 min-1, 0.030 min-1, 0.056 min-1, and 0.071 min-1for PCz, PPy, PTh, PCz-co-PPy-50/50, and PCz-co-PTh-50/50 nanocomposites, respectively, for a 50 mg l-1CIP solution. The catalytic efficiency is attributed to the formation of microwave-induced active species, including hot spots, electrons (e-), holes (h+), superoxide radicals (•O2-), and hydroxyl radicals (•OH). Scavenger analysis verified that •OH and •O2-radicals play a crucial role in CIP degradation. A possible degradation mechanism and pathway for the nanocomposite system is proposed.

环丙沙星(CIP)是一种广泛使用的抗生素,由于其对常规废水处理工艺的抗性,在水体中存在风险。这些药物的积累会破坏水生生态系统,危害水生生物,并导致生态失衡。因此,CIP的降解具有重要的环境意义。研究了咔唑与吡咯共聚纳米复合材料(PCz-co-PPy)和噻吩(PCz-co-PTh)对环丙沙星(CIP)的微波催化降解。采用超声辅助法制备了PCz-co-PPy和PCz-co-PTh纳米复合材料。利用光谱和形态分析对所得纳米复合材料进行了表征。FT-IR和UV-Vis光谱证实了成功的插层和共聚,而FESEM图像显示了链状形貌。将这些共聚物纳米复合材料作为微波活性催化剂用于CIP的降解,在600W微波功率下,pcz -co- py -50/50和PCz-co-PTh-50/50条件下,在21分钟内达到95%的最佳降解效率。在50 mg/L的CIP溶液中,PCz、PPy、PTh、PCz-co-PPy-50/50和PCz-co-PTh-50/50纳米复合物的降解速率常数分别为0.031分钟,0.020分钟,0.030分钟,0.056分钟⁻¹和0.071分钟。这种催化效率归因于微波诱导的活性物质的形成,包括热点、电子(e⁻)、空穴(h⁺)、超氧自由基(•O₂⁻)和羟基自由基(•OH)。清除物分析证实•OH和•O₂毒枭在CIP的降解中起着至关重要的作用。提出了一种可能的降解机理和途径。
{"title":"Elimination of antibiotic contaminants from wastewater using polycarbazole nanocomposites as microwave-activated catalysts.","authors":"Jannatun Zia, Noushi Zaidi, Sapana Jadoun, Ufana Riaz","doi":"10.1088/1361-6528/ada1dd","DOIUrl":"10.1088/1361-6528/ada1dd","url":null,"abstract":"<p><p>Ciprofloxacin (CIP) is a widely used antibiotic, and its presence in water bodies poses a risk due to its resistance to conventional wastewater treatment processes. The accumulation of such pharmaceuticals can disrupt aquatic ecosystems, harm aquatic life, and contribute to ecological imbalances. Therefore, the degradation of CIP is of immense environmental significance. This study presents the microwave-assisted catalytic degradation of the antibiotic drug CIP using nanocomposites of carbazole copolymerized with pyrrole (PCz-co-PPy) and with thiophene (PCz-co-PTh). The PCz-co-PPy and PCz-co-PTh nanocomposites were synthesized through an ultrasound-assisted method. The resulting nanocomposites were characterized using spectral and morphological analyses. FT-IR and UV-Vis spectroscopy confirmed successful intercalation and copolymerization, while FESEM images revealed a chain-like morphology. These copolymer nanocomposites were employed as microwave-active catalysts for CIP degradation, achieving an optimal degradation efficiency of 95% within 21 min using PCz-co-PPy-50/50 and PCz-co-PTh-50/50 at 600 W microwave power. The degradation followed pseudo-first-order kinetics, with rate constants calculated as 0.031 min<sup>-1</sup>, 0.020 min<sup>-1</sup>, 0.030 min<sup>-1</sup>, 0.056 min<sup>-1</sup>, and 0.071 min<sup>-1</sup>for PCz, PPy, PTh, PCz-co-PPy-50/50, and PCz-co-PTh-50/50 nanocomposites, respectively, for a 50 mg l<sup>-1</sup>CIP solution. The catalytic efficiency is attributed to the formation of microwave-induced active species, including hot spots, electrons (e<sup>-</sup>), holes (h<sup>+</sup>), superoxide radicals (•O<sub>2</sub><sup>-</sup>), and hydroxyl radicals (•OH). Scavenger analysis verified that •OH and •O<sub>2</sub><sup>-</sup>radicals play a crucial role in CIP degradation. A possible degradation mechanism and pathway for the nanocomposite system is proposed.</p>","PeriodicalId":19035,"journal":{"name":"Nanotechnology","volume":" ","pages":""},"PeriodicalIF":2.9,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142869674","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Construction and synthesis of NiCo2O4nanozyme for enhanced antibacterial performance. 增强抗菌性能的nico2o4纳米酶的构建与合成。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-12-27 DOI: 10.1088/1361-6528/ad9d49
Luchen Zhang, Shuanglong Wang, Ainong Fang, Pengcheng Hu, Yanhui Zhao, Xiaona Sun, Xiaopeng Lan, Yuan Liu, Chunzhao Liu, Chunlei Liu

Developing effective and low-cost enzyme-like nanomaterials to kill bacteria is vital for human health. Herein, nanorod-assembled NiCo2O4microspheres were prepared though a facile hydrothermal method, andshowed highly enhanced peroxidase-like activity compared to pure Co3O4due to its large surface area and abundant active sites. The NiCo2O4possess the ability to catalyze H2O2to generate large amounts of •O2-, which can be used for bacteriostatic applications. In particular, the antibacterial system combining the spiky NiCo2O4particles and a low concentration of H2O2(100μM) exhibits an excellent bacteriostatic efficiency against bothEscherichia coli(94.44%) andStaphylococcus aureus(93.45%).

开发有效和低成本的类酶纳米材料来杀死细菌对人类健康至关重要。本文通过简单的水热法制备了纳米棒组装的nico2o4微球,由于其表面积大,活性位点丰富,表现出比纯co3o4高的过氧化物酶样活性。nico2o4具有催化h2o2生成大量•O2-的能力,可用于抑菌。其中,尖状nico2o4颗粒与低浓度H2O2(100 μM)相结合的抗菌体系对bothE具有良好的抑菌效果。杆菌(94.44%)and。葡萄球菌(93.45%)强生# xD。
{"title":"Construction and synthesis of NiCo<sub>2</sub>O<sub>4</sub>nanozyme for enhanced antibacterial performance.","authors":"Luchen Zhang, Shuanglong Wang, Ainong Fang, Pengcheng Hu, Yanhui Zhao, Xiaona Sun, Xiaopeng Lan, Yuan Liu, Chunzhao Liu, Chunlei Liu","doi":"10.1088/1361-6528/ad9d49","DOIUrl":"10.1088/1361-6528/ad9d49","url":null,"abstract":"<p><p>Developing effective and low-cost enzyme-like nanomaterials to kill bacteria is vital for human health. Herein, nanorod-assembled NiCo<sub>2</sub>O<sub>4</sub>microspheres were prepared though a facile hydrothermal method, andshowed highly enhanced peroxidase-like activity compared to pure Co<sub>3</sub>O<sub>4</sub>due to its large surface area and abundant active sites. The NiCo<sub>2</sub>O<sub>4</sub>possess the ability to catalyze H<sub>2</sub>O<sub>2</sub>to generate large amounts of •O<sup>2-</sup>, which can be used for bacteriostatic applications. In particular, the antibacterial system combining the spiky NiCo<sub>2</sub>O<sub>4</sub>particles and a low concentration of H<sub>2</sub>O<sub>2</sub>(100<i>μ</i>M) exhibits an excellent bacteriostatic efficiency against both<i>Escherichia coli</i>(94.44%) and<i>Staphylococcus aureus</i>(93.45%).</p>","PeriodicalId":19035,"journal":{"name":"Nanotechnology","volume":" ","pages":""},"PeriodicalIF":2.9,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142813527","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Investigation of EMI-shielding properties of buckypaper manufactured with an easily scalable method. 易扩展法制备巴克纸的电磁屏蔽性能研究。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-12-27 DOI: 10.1088/1361-6528/ada03b
Zaur Nuriakhmetov, Yuri Chernousov, Dmitry Smovzh, Vladimir Andryushchenko

This paper presents a straightforward and easily scalable method for producing buckypapers. These thin films consist of single-walled carbon nanotubes (SWCNTs) dispersed on a PET substrate using an airbrushing technique, followed by solvent evaporation. Notably, this process requires minimal equipment complexity. The study investigates the electrical properties of buckypapers made from both purified and unpurified SWCNTs, as well as chemical vapor deposition graphene. Specifically, we focus on their electromagnetic interference (EMI) shielding effectiveness in theS-band of microwaves (2-4 GHz). To evaluate this, we installed buckypaper and graphene plates within a waveguide cross section. The results show that these buckypapers exhibit high overall shielding effectiveness. It is found that buckypapers based on purified carbon nanotubes have higher shielding parameters (due higher electrical conductivity measured by TRL method) than those based on unpurified CNTs. In summary, our approach offers a practical route for manufacturing effective EMI shielding materials, with potential applications in various technological domains.

本文提出了一种简单且易于扩展的生产纸的方法。巴克纸是通过将分散的SWCNTs悬浮液喷刷到PET基板上,然后进行溶剂蒸发而制成的。这个过程不需要复杂的设备,而且技术上很简单。该研究研究了由SWCNTs(纯化和未纯化的金属杂质)和CVD石墨烯制成的纸的性能,用于在微波(2-4 GHz)的s波段屏蔽EMI。这些材料的板被安装在波导的横截面上。结果表明,该材料具有较高的综合屏蔽效能。研究发现,基于纯化碳纳米管的巴克纸比基于未纯化碳纳米管的巴克纸具有更高的屏蔽参数。这是由于没有金属夹杂物的纯化碳纳米管复合材料具有更高的导电性。所提出的生产巴克纸的方法可以大规模高效地生产屏蔽材料。通过化学气相沉积(CVD)合成的石墨烯板具有独特的性能。石墨烯板的反射系数约为-15 dB,透射系数约为-3 dB。这表明薄板对入射微波功率有较低的反射和显著的吸收。
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引用次数: 0
Comparative performance analysis of mixed metal oxide sensors for dual-sensing leveraging machine learning. 利用机器学习对用于双传感的未混合和混合金属氧化物传感器进行性能比较分析。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-12-27 DOI: 10.1088/1361-6528/ad947e
R Binowesley, Kirubaveni Savarimuthu, M Emimal

This paper presents the synthesis of mixed metal oxide (BaTiO3: ZnO) (B: Z) sensors with various molar ratios using a low-temperature hydrothermal method for dual sensing applications (gas and acceleration). The sensor developed with an equal molar ratio of 1B:1Z, showcases superior performance compared to unmixed and alternative mixed metal oxide sensors. This equilibrium in ratios optimally enhances synergistic effects between elements B and Z, resulting in improved sensing properties. Furthermore, it contributes to structural stability, enhancing performance in gas and acceleration sensing. A decreased band gap of 2.82 eV and a rapid turn-on voltage of 0.18 V were achieved. The acceleration performance of 1B:1Z sensor exhibits a maximum voltage of 2.62 V at a 10 Hz resonant frequency and an output voltage of 2.52 V at 1 g acceleration, achieving an improved sensitivity of 3.889 V g-1. In addition, the proposed gas shows a notable sensor response of ∼63.45% (CO) and 58.29% (CH4) at 10 ppm with a quick response time of 1.19 s (CO) and 8.69 s (CH4) and recovery time of 2.09 s (CO) and 8.69 s (CH4). Challenges in selectivity are addressed using machine learning, employing various classification algorithms. Linear discriminant analysis achieves superior accuracy in differentiating between CO and CH4,reaching 96.6% for CO and 74.6% for CH4at 10 ppm. Understanding these concentration-dependent trends can guide the optimal use of the sensors in different current applications.

本文介绍了采用低温水热法合成不同摩尔比的混合金属氧化物(BaTiO3:ZnO)(B:Z)传感器,用于双重传感应用(气体和加速度)。与未混合和其他混合金属氧化物传感器相比,采用 1B:1Z 等摩尔比开发的传感器性能更优。这种均衡的比例可优化增强 B 和 Z 元素之间的协同效应,从而提高传感性能。此外,它还有助于提高结构稳定性,增强气体和加速度传感性能。这种传感器的带隙减小到 2.82eV,快速开启电压为 0.18V。1B:1Z 传感器的加速性能在谐振频率为 10 Hz 时的最大电压为 2.62 V,在加速度为 1 g 时的输出电压为 2.52 V,灵敏度提高到 3.889 V/g。此外,在 10 ppm 的浓度下,拟议气体的传感器响应速度为 63.45%(CO)和 58.29%(CH4),响应时间分别为 1.19 秒(CO)和 8.69 秒(CH4),恢复时间分别为 2.09 秒(CO)和 8.69 秒(CH4)。利用机器学习和各种分类算法解决了选择性方面的难题。线性判别分析 (LDA) 在区分一氧化碳和甲烷方面取得了卓越的准确性,在 10 ppm 浓度下,一氧化碳和甲烷的准确率分别达到 96.6% 和 74.6%。了解这些随浓度变化的趋势可以指导当前不同应用中传感器的最佳使用。
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引用次数: 0
Advances in nanomaterials for radiation protection in the aerospace industry: a systematic review. 航天工业辐射防护用纳米材料的研究进展:系统综述。
IF 2.9 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-12-27 DOI: 10.1088/1361-6528/ada38f
Antonio Said Webbe Sales, Vinicius de Queiroz Pereira, Airton Natanael Coelho Dias

Nanomaterials stand out for their exceptional properties and innovative potential, especially in applications that protect against space radiation. They offer an innovative approach to this challenge, demonstrating notable properties of radiation absorption and scattering, as well as flexibility and lightness for the development of protective clothing and equipment. This review details the use of polymeric materials, such as polyimides (PIs), which are efficient at attenuating ultraviolet (UV) radiation and atomic oxygen (AO). For example, polyimides show a decrease in elongation at break by 10% after exposure to VUV radiation of 2000 equivalent solar hours (ESH). The thermal stability under vacuum ultraviolet (VUV) irradiation shows that colorless polyimides like CPI-T/Al exhibit an onset degradation temperature of 451°C, while CPI-L/Al shows a degradation onset of 439° C. Additionally, advancements in composite materials for gamma and neutron radiation shielding are covered. Materials such as fluorinated hyperbranched polyimides (FHBPI) display a decomposition temperature of approximately 450°C, which ensures structural integrity during space missions involving radiation. Radiation absorption and scattering properties of these composites are assessed, with materials such as W-Bi2O3 demonstrating a high linear attenuation coefficient (LAC) of 2.5 MeV, enhancing their efficiency in protecting against gamma radiation. Mechanical and optical changes, such as a 15% increase in solar absorbance after exposure to VUV, are critical for prolonged space missions. Moreover, the integration of nanoparticles like graphene and carbon nanotubes into polymers has proven to be an efficient strategy for improving the shielding properties and stability of materials. Nanocomposites like BNTT-Ti display a neutron transmission reduction of 20%, further validating their potential for space applications. Future investigations will focus on optimizing the functionality, manufacturing, and compatibility of composite materials, as well as validating their performance under actual space mission conditions. Collaboration among material scientists, aerospace engineers, and space agencies is vital to transforming laboratory discoveries into viable solutions for radiation protection in space.

纳米材料以其独特的性能和创新潜力脱颖而出,特别是在防止空间辐射的应用中。它们为这一挑战提供了一种创新的方法,展示了显著的辐射吸收和散射特性,以及用于开发防护服和设备的灵活性和轻便性。本文详细介绍了聚酰亚胺(PIs)等高分子材料在紫外线(UV)辐射和原子氧(AO)衰减方面的应用。例如,聚酰亚胺暴露于2000等效太阳小时(ESH)的紫外辐射后,断裂伸长率下降10%。真空紫外(VUV)照射下的热稳定性表明,CPI-T/Al等无色聚酰亚胺的起始降解温度为451℃,CPI-L/Al的起始降解温度为439℃。此外,本文还介绍了用于屏蔽伽马和中子辐射的复合材料的进展。氟化超支化聚酰亚胺(FHBPI)等材料的分解温度约为450°C,可确保在涉及辐射的空间任务期间结构完整。对这些复合材料的辐射吸收和散射性能进行了评估,其中W-Bi2O3等材料显示出2.5 MeV的高线性衰减系数(LAC),提高了它们对伽马辐射的防护效率。机械和光学变化,如暴露于VUV后太阳吸收率增加15%,对长时间的太空任务至关重要。此外,将纳米颗粒(如石墨烯和碳纳米管)集成到聚合物中已被证明是提高材料屏蔽性能和稳定性的有效策略。像BNTT-Ti这样的纳米复合材料显示中子透射率降低了20%,进一步验证了它们在太空应用的潜力。未来的研究将集中在优化复合材料的功能、制造和兼容性,以及验证其在实际空间任务条件下的性能。材料科学家、航空航天工程师和空间机构之间的合作对于将实验室发现转化为空间辐射防护的可行解决方案至关重要。
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