Pub Date : 2025-01-06DOI: 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.
{"title":"Design and characterization of novel graphene-enhanced vapor chambers for lightweight and high-performance electronics cooling.","authors":"Markus Enmark, Murali Murugesan, Hongfeng Zhang, Torbjörn M J Nilsson, Kai J Kallio, Arian Kamal, Johan Liu","doi":"10.1088/1361-6528/ad9f6d","DOIUrl":"https://doi.org/10.1088/1361-6528/ad9f6d","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":19035,"journal":{"name":"Nanotechnology","volume":"36 10","pages":""},"PeriodicalIF":2.9,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142932422","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}
Pub Date : 2025-01-06DOI: 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.
{"title":"Preparation of novel B/ZnO/zeolite nanocomposites by simple combustion method for enhanced dye removal in an aqueous environment.","authors":"Thu Huong Nguyen, Le Van Duong, Anh-Tuan Vu","doi":"10.1088/1361-6528/ada29b","DOIUrl":"10.1088/1361-6528/ada29b","url":null,"abstract":"<p><p>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 m<sup>2</sup>g<sup>-1</sup>) is smaller than that of zeolite (248.78 m<sup>2</sup>g<sup>-1</sup>), but its adsorption capacity is quite high (<i>q</i><sub>max</sub>of 97.6 mg g<sup>-1</sup>). The factors influencing the adsorption process were investigated in detail. Under the optimal conditions (the initial dye concentration of 20 mg l<sup>-1</sup>, the adsorbent content of 0.5 g l<sup>-1</sup>, pH equal 6, and the temperature of 25°C), the removal efficiency (<i>R</i><sub>e</sub>) 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 Δ<i>H</i><sup>o</sup>of -52.423±2.306 kJ mol<sup>-1</sup>indicates the exothermic process and the negative Δ<i>G</i><sup>o</sup>indicates a spontaneous process. At low temperatures, the adsorption of TA proceeds smoother and more effectively, and the negative Δ<i>S</i><sup>o</sup>(-129.638 7.376 J·mol<sup>-1</sup>·K<sup>-1</sup>) indicates a decrease in the degree of freedom of the adsorbed species. The adsorption mechanism was also proposed.</p>","PeriodicalId":19035,"journal":{"name":"Nanotechnology","volume":" ","pages":""},"PeriodicalIF":2.9,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142882320","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}
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.
{"title":"Fabrication of strain-sensing fibers with silver nanoparticles and reduced graphene oxide via wet spinning.","authors":"Xiaoyuan Liu, Qiuyu Xu, Xuepeng Zhang, Wei Jiang, Junmei Li, Runan Pan, Ruochen Song, Lifang Liu","doi":"10.1088/1361-6528/ada2f4","DOIUrl":"10.1088/1361-6528/ada2f4","url":null,"abstract":"<p><p>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 to<i>in situ</i>reduce 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<sup>-3</sup>. 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<sup>-1</sup>. They can stably recognize movements and physiological signals from various parts of the human body, showing good application prospects.</p>","PeriodicalId":19035,"journal":{"name":"Nanotechnology","volume":" ","pages":""},"PeriodicalIF":2.9,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142886010","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}
Pub Date : 2025-01-02DOI: 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.
.
{"title":"Percolation theory-based KMC simulation for scaled Fe-FET based multi-bit computing-in-memory with temperature compensation strategy.","authors":"Qingxiao Zhu, Lihua Xu, Zhidao Zhou, Wei Wei, Pan Xv, Chunmeng Dou, Lingfei Wang, Qing Luo, Ling Li","doi":"10.1088/1361-6528/ada4b8","DOIUrl":"https://doi.org/10.1088/1361-6528/ada4b8","url":null,"abstract":"<p><p>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.
.</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":"142920590","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}
Pub Date : 2025-01-02DOI: 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.
.
{"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.
.</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}
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.
{"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}
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%).
{"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}
Pub Date : 2024-12-27DOI: 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.
{"title":"Investigation of EMI-shielding properties of buckypaper manufactured with an easily scalable method.","authors":"Zaur Nuriakhmetov, Yuri Chernousov, Dmitry Smovzh, Vladimir Andryushchenko","doi":"10.1088/1361-6528/ada03b","DOIUrl":"10.1088/1361-6528/ada03b","url":null,"abstract":"<p><p>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 the<i>S</i>-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.</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":"142846525","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}
Pub Date : 2024-12-27DOI: 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.
{"title":"Comparative performance analysis of mixed metal oxide sensors for dual-sensing leveraging machine learning.","authors":"R Binowesley, Kirubaveni Savarimuthu, M Emimal","doi":"10.1088/1361-6528/ad947e","DOIUrl":"10.1088/1361-6528/ad947e","url":null,"abstract":"<p><p>This paper presents the synthesis of mixed metal oxide (BaTiO<sub>3</sub>: 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<sup>-1</sup>. In addition, the proposed gas shows a notable sensor response of ∼63.45% (CO) and 58.29% (CH<sub>4</sub>) at 10 ppm with a quick response time of 1.19 s (CO) and 8.69 s (CH<sub>4</sub>) and recovery time of 2.09 s (CO) and 8.69 s (CH<sub>4</sub>). Challenges in selectivity are addressed using machine learning, employing various classification algorithms. Linear discriminant analysis achieves superior accuracy in differentiating between CO and CH<sub>4,</sub>reaching 96.6% for CO and 74.6% for CH<sub>4</sub>at 10 ppm. Understanding these concentration-dependent trends can guide the optimal use of the sensors in different current applications.</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":"142682416","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}
Pub Date : 2024-12-27DOI: 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.
{"title":"Advances in nanomaterials for radiation protection in the aerospace industry: a systematic review.","authors":"Antonio Said Webbe Sales, Vinicius de Queiroz Pereira, Airton Natanael Coelho Dias","doi":"10.1088/1361-6528/ada38f","DOIUrl":"https://doi.org/10.1088/1361-6528/ada38f","url":null,"abstract":"<p><p>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.</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":"142896460","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}