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Magnetic response of metal–dielectric hybrid Au-ZnO nanomaterial in the infrared region 金属-电介质杂化Au-ZnO纳米材料在红外区的磁响应
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-06-01 DOI: 10.1016/j.mlblux.2023.100201
B. Gopal Krishna , Dhriti Sundar Ghosh , Sanjay Tiwari

The synthesized photoluminescent and highly dielectric ZnO nanostructures are theoretically investigated as the metamaterial. Herein, the electric and magnetic responses of the ZnO nanomaterial are enhanced by introducing gold into ZnO to form Au-ZnO core–shell nanomaterial. The ZnO nanostructures are studied by optimizing their particle size in the near-infrared and far-field frequency region using Mie theory. The intense light scattering peaks with a peak shift for the Au-ZnO core–shell nanomaterial at the optimized particle size and particular wavelength in the near-infrared region are observed. A strong electric and magnetic pattern for the Au-ZnO core–shell nanomaterial is observed in the near-infrared and far-field frequency region as compared to the ZnO nanoparticles due to the surface plasmon property of the gold. The results pave the way for the design of complex dielectric materials for different optical applications through metamaterial technologies.

从理论上研究了合成的光致发光和高介电性ZnO纳米结构作为超材料。通过在ZnO中引入金,形成Au-ZnO核壳纳米材料,增强了ZnO纳米材料的电响应和磁响应。利用Mie理论对ZnO纳米结构在近红外和远场频率区域的粒径进行优化研究。结果表明,优化后的Au-ZnO核壳纳米材料在近红外区域具有峰移的强光散射峰。与ZnO纳米粒子相比,由于金的表面等离子体特性,在近红外和远场频率区观察到Au-ZnO核壳纳米材料的强电和强磁模式。该结果为通过超材料技术设计不同光学应用的复杂介电材料铺平了道路。
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引用次数: 0
Recycling marine plastic waste to energy storage devices 回收海洋塑料废物为能源储存装置
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-06-01 DOI: 10.1016/j.mlblux.2023.100193
Daisuke Tashima , Takuhiro Kashio , Takuya Eguchi , Seiji Kumagai , Toshiki Tsubota , John D.W. Madden

In this study, a method was developed for the management of marine plastic waste via the production of activated carbon. The specific surface area, micropore volume, and mesopore volume of marine-plastic-based activated carbon prepared at selected temperatures and using selected activator weight ratios were measured, and the specific capacitance and supercapacitor electrode performance were evaluated. At an activation temperature of 800 °C and a raw material to 8 M KOH weight ratio of 1:7, a specific capacitance of 201F/g and a high surface area of 2389 m2/g were obtained. Therefore, marine plastic waste-based activated carbon can be used as the electrode material in supercapacitors.

在本研究中,开发了一种通过生产活性炭来管理海洋塑料废物的方法。测定了在选定温度和活化剂重量比下制备的海洋塑料基活性炭的比表面积、微孔体积和介孔体积,并对其比电容和超级电容器电极性能进行了评价。在活化温度为800℃,原料与8 M KOH的质量比为1:7的条件下,获得了201F/g的比电容和2389 m2/g的高比表面积。因此,海洋塑料垃圾活性炭可以作为超级电容器的电极材料。
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引用次数: 0
Synthesis of Mn3O4 on carbon cloth for flexible supercapacitors 柔性超级电容器用碳布上Mn3O4的合成
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-06-01 DOI: 10.1016/j.mlblux.2023.100198
Liu-Yi Xu, Yi-Jie Gu

Mn3O4@CC electrodes were synthesized via a fast one-step molten salt method for flexible quasi-solid symmetric supercapacitors. Mn3O4 grows rapidly in a high polarity molten salt system and strongly anchors to carbon cloth. The molten salt method can realize sodion embedded in Mn3O4 and then improve the conductivity and capacitance. The results show that the Na-0.9-based supercapacitor exhibits a high capacitance of 1225.7 mF cm−2 at 5 mA cm−2. The preparation method, design strategy on structure of composition in this work will provide a novel route to realize high-performance flexible supercapacitors.

采用快速一步熔盐法合成了柔性准固体对称超级电容器Mn3O4@CC电极。Mn3O4在高极性熔盐体系中生长迅速,并牢固地锚定在碳布上。熔盐法可以实现钠嵌入Mn3O4,从而提高其电导率和电容量。结果表明,na -0.9基超级电容器在5ma cm - 2时具有1225.7 mF cm - 2的高电容。本文所提出的制备方法、组合物结构设计策略将为实现高性能柔性超级电容器提供一条新的途径。
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引用次数: 1
A mechanism for excitation-dependent emission from carbon nanodots 碳纳米点的激发依赖发射机制
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-06-01 DOI: 10.1016/j.mlblux.2023.100195
Manisha Mondal , Subhamay Pramanik

Carbon nanodots (CDs) synthesized via the microwave pyrolysis approach are monodisperse with the nano-size distribution. The CDs show color tunability simply by changing the excitation wavelength. Also, the emission intensity varies with varying different microwave response times. Detail characterizations indicate that the carbon defects that lead to heterogeneous emission levels are responsible for the emission properties of the CDs.

微波热解法制备的碳纳米点呈单分散、纳米级分布。通过改变激发波长,CDs显示出颜色的可调性。发射强度随微波响应时间的变化而变化。详细表征表明,导致非均匀发射水平的碳缺陷是CDs发射特性的原因。
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引用次数: 1
Red luminescence from La2O3:Eu3+ nanophosphor prepared by Sol-Gel method 溶胶-凝胶法制备的La2O3:Eu3+纳米荧光粉的红色发光
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-06-01 DOI: 10.1016/j.mlblux.2023.100205
Pushpa N , M.K. Kokila , K.R. Nagabhushana

Pure and Eu3+ doped La2O3 nanophosphor was synthesized by sol gel process. PL spectra of undoped La2O3 samples shows broad emission peaks between 400 and 600 nm and Eu3+ doped samples show PL emission peaks at 510, 515, 531, 537, 553, 578, 585, 594, 612 and 624 nm. These peaks are attributed to 5D17F2, 5D17F2, 5D07F0, 5D07F1,5D07F2 transitions of Eu3 + ions. The electronic dipole transition corresponding to5D07F2 (624, 612 nm) is stronger than the magnetic dipole transition of 5D07F1 (585, 594 nm) of Eu3+ ions. Luminescence behavior of Eu3+ in La2O3 is analyzed by Judd–Ofelt intensity parameters.

采用溶胶-凝胶法制备了纯Eu3+掺杂La2O3纳米荧光粉。未掺杂La2O3样品的PL光谱在400 ~ 600 nm之间有宽发射峰,而Eu3+掺杂样品的PL光谱在510、515、531、537、553、578、585、594、612和624 nm处有宽发射峰。这些峰归因于Eu3 +离子的5D1→7F2、5D1→7F2、5D0→7F0、5D0→7F1、5D0→7F2跃迁。5D0→7F2(624、612 nm)对应的电子偶极子跃迁比5D0→7F1(585、594 nm)对应的磁偶极子跃迁强。利用judd - felt强度参数分析了Eu3+在La2O3中的发光行为。
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引用次数: 0
Study the hall effect and DC conductivity of CdSe and Te doped CdSe thin films prepared by RF magnetron sputtering method 射频磁控溅射法制备CdSe和Te掺杂CdSe薄膜的霍尔效应和直流电导率研究
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-06-01 DOI: 10.1016/j.mlblux.2023.100204
Devendra Kumar , Chiranji Lal , Dharm Veer , Deshraj Singh , Pawan Kumar , Ram S. Katiyar

CdSe and CdSe:Te thin films were grown on Si p-type substrates by RF magnetron sputtering method. The doping percentage of Tellurium (Te) in CdSe was 7% for the CdSe:Te thin film. The results show that after the doping of Te in the CdSe thin film, the conductivity changes from n-type to p-type and the mobility of the CdSe thin film increased. The conductivity of Te doped CdSe was found to be in order of 10−6 Ω−1 cm−1, while without doping it was 10−5 Ω−1 cm−1. X-ray diffraction (XRD) confirmed the presence of CdSe, Te and Si.

采用射频磁控溅射法在Si - p型衬底上生长了CdSe和CdSe薄膜。碲(Te)在CdSe薄膜中的掺杂率为7%。结果表明,Te掺杂CdSe薄膜后,CdSe薄膜的电导率由n型转变为p型,薄膜的迁移率提高。Te掺杂CdSe的电导率为10−6 Ω−1 cm−1,而未掺杂CdSe的电导率为10−5 Ω−1 cm−1。x射线衍射(XRD)证实了CdSe、Te和Si的存在。
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引用次数: 1
Effect of 100 MeV Ni7+ ion irradiation on photoluminescence of α-A 100MeV Ni7+离子辐照对α-A<mml:mi-mathva光致发光的影响
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-05-01 DOI: 10.1016/j.mlblux.2023.100199
K. R. Nagabhushana, H. Lokesha, S. Satyanarayana Reddy, N. Thejavathi, F. Singh
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引用次数: 0
Americium doping induced self irradiation of SrBPO5: 241Am: Spectroscopic insight 掺汞诱导SrBPO5:241Am的自辐射:光谱透视
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-03-01 DOI: 10.1016/j.mlblux.2023.100185
M. Mohapatra , Santosh K. Gupta

In the present work, 241Am incorporated in SrBPO5 (SBP) host matrix was investigated by various spectroscopic techniques to understand the trap level spectroscopic properties of the system. Photoluminescence (PL) depicted stabilization of Am in +3 oxidation state with low local symmetry. Thermoluminescence (TL) on the other hand suggested that creation of self irradiated defects in SBP:241Am leads to a glow curve around 463 K. Electron spin resonance (ESR) further confirmed the creation of borate radical in axial symmetry on doping ‘Am’ in SBP with hyperfine splitting. We could further propose the mechanism of TL glow curve on doping Am in the SBP lattice.

在本工作中,采用各种光谱技术研究了SrBPO5 (SBP)宿主矩阵中的241Am,以了解该系统的陷阱能级光谱特性。光致发光(PL)描述了Am在+3氧化态的稳定性,具有低局部对称性。另一方面,热释光(TL)表明SBP:241Am中自辐照缺陷的产生导致了463 K左右的发光曲线。电子自旋共振(ESR)进一步证实了在SBP中掺杂“Am”进行超细分裂可以产生轴对称硼酸根。我们可以进一步提出在SBP晶格中掺杂Am的TL发光曲线机理。
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引用次数: 0
Optical characteristics and biosensing application of core@shell nanomaterials core@shell纳米材料的光学特性及生物传感应用
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-03-01 DOI: 10.1016/j.mlblux.2023.100187
Sarita Shaktawat , Kshitij RB Singh , Sushma Thapa , Ranjana Verma , Jay Singh , Ravindra Pratap Singh

Core@shell nanomaterials are a class of materials containing a core and a shell, both at the nanometer scale, as they have become a consequential research interest owing to their optical, electrical, and magnetic properties. Moreover, various core@shell nanomaterials have also emerged in many other fields, such as catalysis, pharmaceuticals, and biomedical due to their less toxicity, surface area, good biocompatibility, adequate penetration power for biological tissue, and selectivity for target molecules. Hence, this review covers the optical properties of core@shell nanomaterials and biosensors based on various core@shell nanomaterials, for example, inorganic@inorganic (Au@Ag), organic@inorganic (polyurethane@Au), inorganic@organic (CeO2@polyaniline), and organic@organic (poly(vinylidene difluoride)@dopamine) for biomedical applications; along with this, it also discusses the advantage and disadvantage of core@shell nanomaterials.

Core@shell纳米材料是一类包含核和壳的材料,都是在纳米尺度上,因为它们已经成为一个重要的研究兴趣,因为它们具有光学,电学和磁性。此外,各种core@shell纳米材料由于其毒性小、表面积大、生物相容性好、对生物组织有足够的穿透能力、对靶分子有选择性等优点,也出现在催化、制药、生物医学等许多其他领域。因此,本综述涵盖了核壳纳米材料的光学性质和基于各种核壳纳米材料的生物传感器,例如:无机无机(Au@Ag),有机无机(聚氨酯@ au),无机有机(ceo2 @聚苯胺)和有机有机(聚(乙烯二氟乙烯)@多巴胺)用于生物医学应用;同时,还讨论了core@shell纳米材料的优缺点。
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引用次数: 0
Data-driven predictive modeling of FeCrAl oxidation 数据驱动的FeCrAl氧化预测建模
IF 1.7 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-03-01 DOI: 10.1016/j.mlblux.2023.100183
Indranil Roy, Subhrajit Roychowdhury, Bojun Feng, Sandipp Krishnan Ravi, Sayan Ghosh, Rajnikant Umretiya, Raul B. Rebak, Daniel M. Ruscitto, Vipul Gupta, Andrew Hoffman

FeCrAl alloys are among the most promising candidates for accident-tolerant fuel cladding material in light water nuclear reactors. Despite their high-temperature oxidation resistance in corrosive environments coupled with their hydrothermal corrosion resistance, a key challenge remains in optimizing the composition of the alloy that can be achieved through statistical analysis. However, the current literature on FeCrAl alloy design lack studies for designing alloys based on oxidation resistance. This study addresses that gap by developing a predictive model for the oxidation of FeCrAl alloys based on an experimental dataset, which lays the groundwork for model-based optimization for alloy composition.

铁铁合金是轻水反应堆耐事故燃料包壳材料中最有前途的候选材料之一。尽管它们在腐蚀环境中具有高温抗氧化性和水热腐蚀性,但一个关键的挑战仍然是通过统计分析来优化合金的成分。然而,目前关于铁铁合金设计的文献缺乏基于抗氧化设计合金的研究。本研究通过开发基于实验数据集的FeCrAl合金氧化预测模型来解决这一空白,这为基于模型的合金成分优化奠定了基础。
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引用次数: 3
期刊
Materials Letters: X
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