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Manipulating polarization attenuation in NbS2–NiS2 nanoflowers through homogeneous heterophase interface engineering toward microwave absorption with shifted frequency bands 通过同质异相界面工程操纵 NbS2-NiS2 纳米流中的偏振衰减,实现频带偏移的微波吸收
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2024-12-01 DOI: 10.1016/j.nanoms.2024.05.003
Yiru Fu , Yuping Wang , Junye Cheng , Yao Li , Jing Wang , Yongheng Jin , Deqing Zhang , Guangping Zheng , Maosheng Cao
Homogeneous heterogeneous (heterophase) interfaces regulated with low energy barriers have a fast response to applied electric fields and could provide a unique interfacial polarization, which facilitate the transport of electrons across the substrate. Such regulation on the interfaces is effective in modulating electromagnetic wave absorbing materials. Herein, we construct NbS2–NiS2 heterostructures with NiS2 nanoparticles uniformly grown in NbS2 hollow nanospheres, and such particular structure enhances the interfacial polarization. The strong electron transfer at the interface promotes electron transport throughout the material, which results in less scattering, promotes conduct ion loss and dielectric polarization relaxation, improves dielectric loss, and results in a good impedance matching of the material. Consequently, the absorbing band may be successful tuned. By regulating the amount of NiS2, the heterogeneous interface is finely alternated so that the overall wave-absorbing performance is shifted to lower frequencies. With a NiS2 content of 15 ​wt% and an absorber thickness of 1.84 ​mm, the minimum reflection loss at 14.56 ​GHz is −53.1 ​dB, and the effective absorption bandwidth is 5.04 ​GHz; more importantly, the minimum reflection loss in different bands is −20 dB, and the microwave energy absorption rate reaches 99% when the thickness is about 1.5–4.5 ​mm. This work demonstrates the construction of homogeneous heterostructures is effective in improving the electromagnetic absorption properties, providing guideline for the synthesis of highly efficient electromagnetic absorbing materials.
低能垒调节的均质异质(异相)界面对外加电场有快速响应,并能提供独特的界面极化,从而促进电子在衬底上的传输。这种界面上的调节对电磁波吸收材料的调制是有效的。本文将NiS2纳米颗粒均匀生长在NbS2空心纳米球中,构建了NbS2 - NiS2异质结构,这种特殊的结构增强了界面极化。界面处的强电子转移促进了电子在整个材料中的传递,从而减少了散射,促进了导电离子损失和介电极化弛豫,改善了介电损耗,使材料具有良好的阻抗匹配。因此,吸收带可以被成功调谐。通过调节NiS2的量,非均匀界面被精细地交替,从而使整体吸波性能转移到较低的频率。NiS2含量为15 wt%,吸收体厚度为1.84 mm时,在14.56 GHz处的最小反射损耗为- 53.1 dB,有效吸收带宽为5.04 GHz;更重要的是,不同波段的最小反射损耗为−20 dB,当厚度约为1.5 ~ 4.5 mm时,微波能量吸收率达到99%。本工作证明了均质异质结构的构建对提高电磁吸收性能是有效的,为高效电磁吸收材料的合成提供了指导。
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引用次数: 0
Current strategic development of single-atom electrocatalyst in sensor construction: A mini-review 单原子电催化剂在传感器构建中的战略发展现状:微型综述
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2024-12-01 DOI: 10.1016/j.nanoms.2024.06.007
Mohanraj Jagannathan , Sungbo Cho
With the development of advanced catalysts, the assessment of emerging single-atom-based electrochemical catalysts (SAECs) has significantly increased owing to their similarity to natural enzymes. They hold substantial potential for the design and construction of electrochemical sensing platforms. The fabrication of single-atom-based electrodes revealed their potential for sensitive and selective analyses. Among various nanomaterials, transition metal element-based single-atom, bimetallic single-atom, and metal-free single-atom, each with well-defined active sites, exhibit enhanced catalytic activity, selectivity, and stability. The rational construction of the composition, size, and the strategic development of single-atom electrocatalysts on carbon platforms to enable them to function effectively in complex environments and demonstrate their efficiency between the active sites and electrode construction strategies. Unlike traditional catalysts, SAECs are considered to potential substitutes for natural enzymes. This perspective has been described in a mini-review that highlights recent developments in transition metal elements-based single/bimetallic single atoms and metal-free single atoms anchored on carbon nanostructures. Additionally, there has been a rise in the fabrication of printed electrodes as sensing platforms for biomedical, environmental, and food toxin detection. The challenges and prospects for SAECs in multiple sensing applications are also concisely elaborated.
随着先进催化剂的发展,新兴的单原子电化学催化剂(SAECs)因其与天然酶的相似性而受到越来越多的重视。它们在电化学传感平台的设计和构建方面具有巨大的潜力。单原子电极的制造显示了它们在敏感和选择性分析方面的潜力。在各种纳米材料中,基于过渡金属元素的单原子、双金属单原子和不含金属的单原子都具有明确的活性位点,表现出增强的催化活性、选择性和稳定性。合理构建碳平台单原子电催化剂的组成、尺寸和策略发展,使其能够在复杂环境中有效发挥作用,并在活性位点和电极构建策略之间展示其效率。与传统催化剂不同,saec被认为是天然酶的潜在替代品。这一观点已经在一篇小型综述中进行了描述,重点介绍了基于过渡金属元素的单/双金属单原子和锚定在碳纳米结构上的无金属单原子的最新进展。此外,作为生物医学、环境和食物毒素检测的传感平台,印刷电极的制造也有所增加。简要阐述了saec在多种传感应用中的挑战和前景。
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引用次数: 0
Nanoscale air channel devices- inheritance and breakthrough of vacuum tube 纳米级空气通道装置--真空管的继承与突破
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2024-12-01 DOI: 10.1016/j.nanoms.2024.01.002
Baihong Chen , Linjie Fan , Jinshun Bi , Zhiqiang Li , Ziming Xu , Sandip Majumdar
The nanoscale air channel device (NACD) has recently gained significant attention as a novel vacuum electronic that can be fabricated through nanofabrication technologies. Here, the research and progress of the NACD since it was reviewed, with a focus on working mechanism analysis, nanofabrication technologies, device structure optimization, electrode materials and simulation approach. Furthermore, the application fields and future development of NACD were summarized and prospected. The NACDs are expected to surpass the physical limits of traditional solid transistors due to its advantages such as smaller heat loss, high-speed, resistance to harsh environments.
纳米级空气通道器件(NACD)作为一种新型的真空电子器件,可以通过纳米制造技术制造,近年来引起了人们的广泛关注。本文综述了NACD自诞生以来的研究进展,重点从工作机理分析、纳米加工技术、器件结构优化、电极材料和模拟方法等方面进行了综述。并对NACD的应用领域和未来发展进行了总结和展望。nnacd具有热损耗小、速度快、耐恶劣环境等优点,有望超越传统固体晶体管的物理极限。
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引用次数: 0
Highly luminescent all-inorganic lead-free AgInS2/ZnS QDs for multicolor and multistage anti-counterfeiting and encryption 高发光全无机无铅AgInS2/ZnS量子点,用于多色多级防伪加密
IF 17.9 2区 材料科学 Q1 Engineering Pub Date : 2024-11-25 DOI: 10.1016/j.nanoms.2024.10.005
Pawan Kumar , Lei Jin , Gurpreet Singh Selopal , Omar Abdelkarim , Jiabin Liu , David Barba , Aycan Yurtsever , Zhiming M. Wang , Federico Rosei
We describe the design and synthesis of eco-friendly AgInS2/ZnS QDs via a facile one-pot synthesis method for application in encryption and anti-counterfeiting. A significant enhancement in PLQY (up to 45 ​%) and stability are observed with increased ZnS shell thickness. By varying the Ag:In composition from 1:2 to 1:0.25, the PL emission of AgInS2/ZnS QDs can be tuned from the visible to NIR (up to 900 ​nm). The ink fabricated with AgInS2/ZnS QDs shows greater thermal and water stability compared to AgInS2 QDs. The patterns printed with these luminescent inks show excellent water and thermal stability and the capability to print on surfaces of any type and color, making them promising for practical use. These printed patterns are completely transparent/invisible in normal light and visible under 254 ​nm, 365 ​nm and 464 ​nm (blue LED) illumination. These features offer rapid responsive and multi-layered information encryption, and sophisticated anti-counterfeiting.
我们描述了一种简单的一锅合成方法,设计和合成了生态友好的AgInS2/ZnS量子点,用于加密和防伪。随着ZnS外壳厚度的增加,PLQY(高达45%)和稳定性显著增强。通过改变AgInS2/ZnS量子点的Ag:In组成从1:2到1:0.25,可以将AgInS2/ZnS量子点的PL发射从可见光调谐到近红外(高达900 nm)。与AgInS2量子点相比,用AgInS2/ZnS量子点制备的油墨表现出更高的热稳定性和水稳定性。用这些发光油墨印刷的图案具有优异的水和热稳定性,并且能够在任何类型和颜色的表面上印刷,这使它们具有实际应用的前景。这些印刷图案在正常光线下完全透明/不可见,在254 nm, 365 nm和464 nm(蓝色LED)照明下可见。这些功能提供快速响应和多层信息加密,以及复杂的防伪。
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引用次数: 0
Hybridization of polyoxometalates and metal-organic frameworks for effective tumor chemodynamic therapy and sonodynamic therapy 多金属氧酸盐和金属有机框架的杂交用于有效的肿瘤化学动力治疗和声动力治疗
IF 17.9 2区 材料科学 Q1 Engineering Pub Date : 2024-11-20 DOI: 10.1016/j.nanoms.2024.10.015
Runjie Wang , Zhengya Yue , Wei Feng , Yuan Sun , Xin Hai , Lei Wang , Tiedong Sun
Metal-organic frameworks (MOFs) with high porosity, specific surface area, and unique topologies are highly regarded for their applications in photocatalysis, medical treatment, and environmental pollutant degradation. However, due to the limitations of the tumor microenvironment (TME), traditional MOFs have limited efficacy in this environment. This paper designs multi-metal oxide-based heterostructure POMOFs nanoreactors with a nesting doll-like structure. This new structure not only exhibits therapeutic effects in TME but also utilizes ultrasound (US) to enhance the release of reactive oxygen species (ROS) for CDT&SDT co-therapy, becoming an effective sound sensitizer for destroying tumor cells. In summary, our study proposes an idea for constructing multi-metal oxide-based heterostructure MOFs nanoreactors material with a nesting doll-like structure to enhance ROS release and synergistically treat tumor diseases.
金属有机骨架(mof)具有高孔隙率、比表面积和独特的拓扑结构,在光催化、医疗和环境污染物降解等方面具有广泛的应用前景。然而,由于肿瘤微环境(TME)的限制,传统mof在这种环境下的疗效有限。本文设计了具有套娃状结构的多金属氧化物异质结构多金属氧化物纳米反应器。这种新结构不仅在TME中表现出治疗效果,而且利用超声(US)增强活性氧(ROS)的释放,用于cdt和SDT的联合治疗,成为一种有效的破坏肿瘤细胞的声敏剂。综上所述,我们的研究提出了构建具有套娃娃状结构的多金属氧化物异质结构mof纳米反应器材料,以增强ROS释放,协同治疗肿瘤疾病的思路。
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引用次数: 0
Recent engineering strategies for enhancing C2+ product formation in copper-catalyzed CO2 electroreduction 铜催化CO2电还原中提高C2+产物形成的最新工程策略
IF 17.9 2区 材料科学 Q1 Engineering Pub Date : 2024-10-22 DOI: 10.1016/j.nanoms.2024.09.001
Muhammad Shakir Hussain , Sheraz Ahmed , Muhammad Irshad , Syeda Sidra Bibi , Muhammad Asif , Farooq Sher , Muhammad Kashif Khan
The conversion of carbon dioxide (CO2) into hydrocarbons through electrochemical CO2 reduction reaction (eCO2RR) shows a promising method to reduce CO2 levels and decrease reliance on fossil fuels in the years to come. Copper-based electrocatalysts exhibit a pronounced inclination for C–C coupling, drawing considerable interest as a favored metal catalyst for generating C2+ products through CO2RR. However, CO2RR still has some obstacles including product selectivity, higher overpotential, low Faradic efficiency (FE), stability, and current density (CD). Therefore, advancement in this field enables us to comprehend the complex multi-proton electron transfer during C–C coupling and engineering strategies to improve FE and CD. Herein, this review presents some key features of Cu-based catalysts as an electrocatalyst for C2 product formation while addressing the industrial challenges that hinder commercialization of CO2RR. In addition, recent strategies on Cu-based catalysts, synthesis strategies, advanced characterizations, and mechanistic investigations via theoretical simulations have been presented. Furthermore, recent approaches towards the composition, oxidation states, and active facets have been presented. Thus, the most favorable mechanism and possible pathways to synthesize C2+ products have been explained using theoretical calculations.
通过电化学二氧化碳还原反应(eCO2RR)将二氧化碳(CO2)转化为碳氢化合物,显示出在未来几年减少二氧化碳水平和减少对化石燃料依赖的一种很有前途的方法。铜基电催化剂表现出明显的C-C偶联倾向,作为通过CO2RR生成C2+产物的首选金属催化剂,引起了人们的极大兴趣。然而,CO2RR仍然存在一些障碍,包括产物选择性,高过电位,低法拉迪效率(FE),稳定性和电流密度(CD)。因此,这一领域的进展使我们能够理解C-C耦合过程中复杂的多质子电子转移以及提高FE和CD的工程策略。本文介绍了cu基催化剂作为C2产物形成电催化剂的一些关键特征,同时解决了阻碍CO2RR商业化的工业挑战。此外,本文还介绍了铜基催化剂的最新发展策略、合成策略、先进的表征以及通过理论模拟进行的机理研究。此外,最近对其组成、氧化态和活性方面的研究也有所进展。因此,用理论计算解释了合成C2+产物的最有利的机理和可能的途径。
{"title":"Recent engineering strategies for enhancing C2+ product formation in copper-catalyzed CO2 electroreduction","authors":"Muhammad Shakir Hussain ,&nbsp;Sheraz Ahmed ,&nbsp;Muhammad Irshad ,&nbsp;Syeda Sidra Bibi ,&nbsp;Muhammad Asif ,&nbsp;Farooq Sher ,&nbsp;Muhammad Kashif Khan","doi":"10.1016/j.nanoms.2024.09.001","DOIUrl":"10.1016/j.nanoms.2024.09.001","url":null,"abstract":"<div><div>The conversion of carbon dioxide (CO<sub>2</sub>) into hydrocarbons through electrochemical CO<sub>2</sub> reduction reaction (eCO<sub>2</sub>RR) shows a promising method to reduce CO<sub>2</sub> levels and decrease reliance on fossil fuels in the years to come. Copper-based electrocatalysts exhibit a pronounced inclination for C–C coupling, drawing considerable interest as a favored metal catalyst for generating C<sub>2+</sub> products through CO<sub>2</sub>RR. However, CO<sub>2</sub>RR still has some obstacles including product selectivity, higher overpotential, low Faradic efficiency (FE), stability, and current density (CD). Therefore, advancement in this field enables us to comprehend the complex multi-proton electron transfer during C–C coupling and engineering strategies to improve FE and CD. Herein, this review presents some key features of Cu-based catalysts as an electrocatalyst for C<sub>2</sub> product formation while addressing the industrial challenges that hinder commercialization of CO<sub>2</sub>RR. In addition, recent strategies on Cu-based catalysts, synthesis strategies, advanced characterizations, and mechanistic investigations via theoretical simulations have been presented. Furthermore, recent approaches towards the composition, oxidation states, and active facets have been presented. Thus, the most favorable mechanism and possible pathways to synthesize C<sub>2+</sub> products have been explained using theoretical calculations.</div></div>","PeriodicalId":33573,"journal":{"name":"Nano Materials Science","volume":"8 1","pages":"Pages 207-233"},"PeriodicalIF":17.9,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146057504","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
MXene multi-functionalization of polyrotaxane based PCMs and the applications in electronic devices thermal management 基于聚二十六烷的 PCM 的 MXene 多功能化及其在电子设备热管理中的应用
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2024-10-01 DOI: 10.1016/j.nanoms.2023.12.004
Guangzhong Yin , Alba Marta López , Ignacio Collado , Antonio Vázquez-López , Xiang Ao , Jose Hobson , Silvia G. Prolongo , Deyi Wang
The aim of this work was to improve the thermal conductivity and electromagnetic shielding of the leakage proof phase change materials (PCMs), in which a polyrotaxane (PLR) was used as a support material to encapsulate PEG 1k or PEG 6k and MXene as multi-functional filler. The PCMs can be processed conveniently by a hot press and the PEG 1k containing samples showed excellent flexibility. We conducted a systematic evaluation of the phase transition behavior of the material, thermal conductivity and electromagnetic shielding performance tests. Notably, the PCMs achieved a high enthalpy values (123.9–159.6 ​J/g). The PCMs exhibited an increase of 44.3 ​%, and 137.5 ​% in thermal conductivity values with higher MXene content (5 ​wt%) for PLR-PEG6k and PLR-PEG1k, respectively, and show high shape stability and no leakage during and after phase transition. The introduction of MXene can significantly improve the electromagnetic shielding performance of PCM composites. Typically, higher conductive samples (samples which contain high MXene contents) offer a higher EMI SE shielding, reaching a maximum of 4.67 ​dB at 5.6 ​GHz for PLR-1K-MX5. These improvements solve the main problems of organic PEG based PCMs, thus making PLR-PEG-MXene based PCMs good candidates for thermoregulators of both solid-state disks and smart phone. It is worth pointing out that the sample PLR-1k-MX5 can decrease 4.3 ​°C of the reference temperature during cellphone running. Moreover, the temperature of the protecting sheet in the simulated solid state disk with PCM was significantly lower (showing a decreasing of 7.9 ​°C) compared with the blank sample.
这项研究的目的是提高防漏相变材料(PCMs)的导热性和电磁屏蔽性,其中使用了聚洛他赛(PLR)作为支撑材料,包裹 PEG 1k 或 PEG 6k,并使用 MXene 作为多功能填料。这种 PCM 可方便地通过热压工艺进行加工,含有 PEG 1k 的样品显示出极佳的柔韧性。我们对材料的相变行为、热导率和电磁屏蔽性能测试进行了系统评估。值得注意的是,PCM 达到了很高的焓值(123.9-159.6 J/g)。PLR-PEG6k 和 PLR-PEG1k 的 MXene 含量越高(5 wt%),PCM 的热导率值分别增加了 44.3% 和 137.5%,并且在相变过程中和相变后显示出较高的形状稳定性和无泄漏性。引入 MXene 可显著提高 PCM 复合材料的电磁屏蔽性能。通常情况下,导电性较高的样品(MXene 含量较高的样品)具有更高的电磁干扰屏蔽性能,PLR-1K-MX5 在 5.6 GHz 时的电磁干扰屏蔽性能最高可达 4.67 dB。这些改进解决了基于有机 PEG 的 PCM 的主要问题,从而使基于 PLR-PEG-MXene 的 PCM 成为固态磁盘和智能手机温度调节器的理想候选材料。值得注意的是,样品 PLR-1k-MX5 在手机运行过程中可将参考温度降低 4.3 °C。此外,与空白样品相比,含有 PCM 的模拟固态盘中保护片的温度明显降低(降低了 7.9 °C)。
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引用次数: 0
Structure transformation induced bi-component Co–Mo/A-Co(OH)2 as highly efficient hydrogen evolution catalyst in alkaline media 结构转变诱导的双组分 Co-Mo/A-Co(OH)2 作为碱性介质中的高效氢进化催化剂
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2024-10-01 DOI: 10.1016/j.nanoms.2023.11.006
Yingqing Ou , Lu Liu , Xiao Peng , Lili Zhang , Zhongwen Ou , Wendong Zhang , Yunhuai Zhang
Elucidating the inherent origins of the sluggish hydrogen evolution reaction (HER) kinetics in alkaline media and developing high-performance electrocatalysts are fundamental for the advances of conventional alkaline water electrolyzers and emerging anion exchange membrane (AEM) electrolyzers. Here we present a facile electrochemical modification strategy for the synthesis of bi-component Co–Mo(18%)/A-Co(OH)2 catalyst toward efficient HER catalysis in alkaline media. Porous Co–Mo alloys with adjustable Mo/Co atomic ratio are first prepared by H2-assisted cathodic electrodeposition. By virtue of the appropriate electronic structure and hydrogen binding energy, Co–Mo(18%) is the most HER active among the alloys and is further activated by a constant-current electrochemical modification process. Physical characterizations reveal the formation of amorphous Co(OH)2 nanoparticles on the surface. Electrokinetic analysis combined with theoretical calculations reveal that the in-situ formed Co(OH)2 can efficiently promote the water dissociation, resulting in accelerated Volmer-step kinetics. As a result, the Co–Mo(18%)/A-Co(OH)2 simultaneously achieves the optimization of the two factors dominating alkaline HER activity, i.e., water dissociation and hydrogen adsorption/desorption via the bifunctional synergy of the bi-components. The high HER activity (η10 of 47 ​mV at 10 ​mA ​cm−2) of Co–Mo(18%)/A-Co(OH)2 is close to benchmark Pt/C catalyst and comparable or superior to the most active non-noble metal catalysts.
阐明碱性介质中氢气进化反应(HER)动力学迟缓的内在原因并开发高性能电催化剂是传统碱性水电解槽和新兴阴离子交换膜(AEM)电解槽发展的基础。在此,我们提出了一种简便的电化学改性策略,用于合成双组分 Co-Mo(18%)/A-Co(OH)2催化剂,以在碱性介质中实现高效 HER 催化。首先通过 H2- 辅助阴极电沉积制备出具有可调 Mo/Co 原子比的多孔 Co-Mo 合金。凭借适当的电子结构和氢结合能,Co-Mo(18%) 是合金中最具 HER 活性的一种,并通过恒流电化学改性过程进一步激活。物理特性分析表明,表面形成了无定形的 Co(OH)2 纳米颗粒。电动力学分析和理论计算显示,原位形成的 Co(OH)2 能有效促进水的解离,从而加速 Volmer 步动力学。因此,Co-Mo(18%)/A-Co(OH)2 通过双组分的双功能协同作用,同时优化了主导碱性 HER 活性的两个因素,即水解离和氢吸附/解吸。Co-Mo(18%)/A-Co(OH)2 的高氢氧还原活性(η10 为 47 mV,10 mA cm-2)接近基准 Pt/C 催化剂,可与活性最高的非贵金属催化剂媲美或更胜一筹。
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引用次数: 0
Low-frequency and dual-band microwave absorption properties of novel VB-group disulphides (3R–TaS2) nanosheets 新型 VB 族二硫化物 (3R-TaS2) 纳米片的低频和双波段微波吸收特性
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2024-10-01 DOI: 10.1016/j.nanoms.2024.05.011
Liquan Fan , Honglin Ai , Meiye Jiao , Yao Li , Yongheng Jin , Yiru Fu , Jing Wang , Yuwei Wang , Deqing Zhang , Guangping Zheng , Junye Cheng
As electromagnetic technology advances and demand for electronic devices grows, concerns about electromagnetic pollution intensify. This has spurred focused research on innovative electromagnetic absorbers, particularly chalcogenides, noted for their superior absorption capabilities. In this study, we successfully synthesize 3R–TaS2 nanosheets using a straightforward calcination method for the first time. These nanosheets exhibit significant absorption capabilities in both the C-band (4–8 ​GHz) and Ku-band (12–18 ​GHz) frequency ranges. By optimizing the calcination process, the complex permittivity of TaS2 is enhanced, specifically for those synthesized at 1000 ​°C for 24 ​h. The nanosheets possess dual-band absorption properties, with a notable minimum reflection loss (RLmin) of −41.4 ​dB in the C-band, and an average absorption intensity exceeding 10 ​dB in C- and Ku-bands, in the absorbers with a thickness of 5.6 ​mm. Additionally, the 3R–TaS2 nanosheets are demonstrated to have an effective absorption bandwidth of 5.04 ​GHz (3.84–8.88 ​GHz) in the absorbers with thicknesses of 3.5–5.5 ​mm. The results highlight the multiple reflection effects in 3R–TaS2 as caused by their stacked structures, which could be promising low-frequency absorbers.
随着电磁技术的发展和对电子设备需求的增长,人们对电磁污染的担忧日益加剧。这激发了对创新型电磁吸收剂的重点研究,尤其是以其卓越的吸收能力而著称的铬化砷化物。在本研究中,我们首次采用直接煅烧法成功合成了 3R-TaS2 纳米片。这些纳米片在 C 波段(4-8 GHz)和 Ku 波段(12-18 GHz)频率范围内均表现出显著的吸收能力。通过优化煅烧过程,TaS2 的复介电常数得到了提高,尤其是在 1000 °C 下合成 24 小时的纳米片。这种纳米片具有双波段吸收特性,在 C 波段的最小反射损耗(RLmin)为 -41.4 dB,而在 C 波段和 Ku 波段,厚度为 5.6 mm 的吸收体的平均吸收强度超过 10 dB。此外,在厚度为 3.5-5.5 毫米的吸收器中,3R-TaS2 纳米片的有效吸收带宽为 5.04 GHz(3.84-8.88 GHz)。这些结果凸显了 3R-TaS2 的叠层结构所产生的多重反射效应,有望成为一种低频吸收器。
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引用次数: 0
Revisiting the mitigation of coke formation: Synergism between support & promoters' role toward robust yield in the CO2 reformation of methane 重新审视焦炭形成的缓解问题:在甲烷的二氧化碳转化过程中,支持和促进剂对提高产量的协同作用
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2024-10-01 DOI: 10.1016/j.nanoms.2023.10.005
Zahra Taherian , Vahid Shahed Gharahshiran , Xiaoxuan Wei , Alireza Khataee , Yeojoon Yoon , Yasin Orooji
CO2 reformation of methane (CRM) and CO2 methanation are two interconnected processes with significant implications for greenhouse gas reduction and sustainable energy production for industrial purposes. While Ni-based catalysis suffers from poor stability due to coke formation or sintering, we report a super stable remedy. The active sites of mesoporous MgO were loaded using wet impregnation. The incorporation of Ni and promoters altered the physical features of the catalysts. Sm–Ni/MgO showed the smallest crystallite size, specific surface area, and pore volume. The Sm–Ni/MgO catalyst was selected as the most suitable candidate for CRM, with 82 ​% CH4 and H2/CO ratio of approximately 100 ​% and also for CO2 methanation with the conversion of carbon dioxide (82 ​%) and the selectivity toward methane reaches 100 ​% at temperatures above 300 C. Furthermore, the Sm–Ni/MgO catalyst was stable for 900 ​min of continuous reaction, without significant carbon deposition. This stability was largely due to the high oxygen mobility on the catalyst surface in the presence of Sm. Overall, we demonstrated the efficacy of using promoted Ni catalysts supported by mesoporous magnesia for the improved reformation of greenhouse gases.
甲烷的二氧化碳重整(CRM)和二氧化碳甲烷化是两个相互关联的过程,对减少温室气体排放和工业用可持续能源生产具有重要意义。镍基催化剂因形成焦炭或烧结而稳定性差,而我们报告了一种超稳定的补救方法。介孔氧化镁的活性位点是通过湿法浸渍负载的。镍和促进剂的加入改变了催化剂的物理特性。Sm-Ni/MgO 的结晶尺寸、比表面积和孔体积最小。Sm-Ni/MgO催化剂被选为 CRM 的最合适候选催化剂,其 CH4 转化率为 82%,H2/CO 比率约为 100%,还可用于 CO2 甲烷化,二氧化碳转化率为 82%,在温度高于 300 ᵒC时,对甲烷的选择性达到 100%。此外,Sm-Ni/MgO 催化剂在连续反应 900 分钟后保持稳定,没有明显的碳沉积。这种稳定性主要归功于催化剂表面在 Sm 存在下的高氧流动性。总之,我们证明了使用介孔镁支撑的促进镍催化剂在改善温室气体转化方面的功效。
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Nano Materials Science
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