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Ultrastrong silk fabric ionogel-sensor for strain/ temperature/ tactile multi-mode sensing 用于应变/温度/触觉多模式传感的超强丝织物离子凝胶传感器
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-06-01 DOI: 10.1016/j.nanoms.2025.06.005
Shu Wang , Jiangling Ning , Jianyu Pu , Changjie Wei , Yuping Yuan , Songqi Yao , Yuantao Zhang , Ziwen Jing , Chenxing Xiang , Xinglong Gong , Zhi Li , Ning Hu
Ionogels have demonstrated substantial applications in smart wearable systems, soft robotics, and biomedical engineering due to the exceptional ionic conductivity and optical transparency. However, achieving ionogels with desirable mechanical properties, environmental stability, and multi-mode sensing remains challenging. Here, we propose a simple strategy for the fabrication of multifunctional silk fabric-based ionogels (BSFIGs). The resulting fabric ionogels exhibits superior mechanical properties, with high tensile strength (11.3 ​MPa) and work of fracture (2.53 ​MJ/m3). And its work of fracture still has 1.42 ​MJ/m3 as the notch increased to 50 ​%, indicating its crack growth insensitivity. These ionogels can be used as sensors for strain, temperature, and tactile multi-mode sensing, demonstrating a gauge factor of 1.19 and a temperature coefficient of resistance of −3.17/°C-1. Furthermore, these ionogels can be used for the detection of different roughness and as touch screens. The ionogels also exhibit exceptional optical transmittance and environmental stability even at −80 ​°C. Our scalable fabrication process broadens the application potential of these multifunctional ionogels in diverse fields, from smart systems to extreme environments.
离子凝胶由于其优异的离子导电性和光学透明性,在智能可穿戴系统、软机器人和生物医学工程中得到了广泛的应用。然而,实现具有理想机械性能、环境稳定性和多模式传感的电离层凝胶仍然具有挑战性。在这里,我们提出了一种简单的制造多功能丝绸织物离子凝胶(BSFIGs)的策略。所得织物离子凝胶具有优异的力学性能,具有较高的抗拉强度(11.3 MPa)和断裂功(2.53 MJ/m3)。当缺口增大到50%时,其断裂功仍为1.42 MJ/m3,表明其裂纹扩展不敏感。这些离子凝胶可以用作应变、温度和触觉多模式传感的传感器,其测量系数为1.19,电阻温度系数为- 3.17/°C-1。此外,这些离子凝胶可以用于检测不同的粗糙度和作为触摸屏。即使在- 80°C下,离子凝胶也表现出优异的光学透过率和环境稳定性。我们的可扩展制造工艺拓宽了这些多功能电离层凝胶在不同领域的应用潜力,从智能系统到极端环境。
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引用次数: 0
ZnAl-LDH film for self-powered ultraviolet photodetection 用于自供电紫外光检测的 ZnAl-LDH 薄膜
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-06-01 DOI: 10.1016/j.nanoms.2024.05.001
Simin Sun , Yuan Zhang , Qiyue Gao , Nana Zhang , PingAn Hu , Wei Feng
Self-powered photoelectrochemical-type (PEC) ultraviolet photodetectors (UV PDs) have been rapidly developed owing to their low-cost fabrication and good photodetection. However, achieving high-performance and self-powered PEC UV PDs based on an individual material is still challenging. Therefore, developing more wide bandgap semiconductors for high-performance PEC UV PDs is attractive. Here, we demonstrate that ZnAl-LDH is suitable for self-powered PEC UV PDs with high responsivity and excellent wavelength selectivity for the first time. The responsivity is 29.25 ​mA/W (254 ​nm irradiation) and the UV/visible rejection ratio is 1037, surpassing most PEC UV PDs. Furthermore, the PEC UV PDs have fast response, good stability, and underwater optical communication capability. This work offers more chances for the development of high-performance PEC UV PDs and demonstrates the potential application of ZnAl-LDH in underwater optoelectronic devices.
自供电型光电化学型紫外探测器(UV pd)因其制造成本低、光探测性能好而得到了迅速发展。然而,基于单个材料实现高性能和自供电的PEC UV pd仍然具有挑战性。因此,开发更多的宽禁带半导体用于高性能PEC UV pd是有吸引力的。本文首次证明了ZnAl-LDH适用于具有高响应性和优异波长选择性的自供电PEC UV pd。响应度为29.25 mA/W (254 nm辐照),UV/可见光抑制比为1037,超过了大多数PEC UV pd。此外,PEC UV pd具有响应快、稳定性好、水下光通信能力强等特点。这项工作为高性能PEC UV pd的发展提供了更多的机会,并展示了ZnAl-LDH在水下光电器件中的潜在应用。
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引用次数: 0
The integration of microelectronic and photonic circuits on a single silicon chip for high-speed and low-power optoelectronic technology 在单个硅芯片上集成微电子和光子电路,实现高速和低功耗光电技术
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-06-01 DOI: 10.1016/j.nanoms.2024.04.011
Rajeev Gupta , Ajay Kumar , Manoj Kumar , Rajesh Singh , Anita Gehlot , Purnendu Shekhar Pandey , Neha Yadav , Kailash Pandey , Ashish Yadav , Neha Gupta , Ranjeet Brajpuriya , Shalendra Kumar , Ajay Singh Verma , Tanuj Kumar , Yongling Wu , Zheng Hongyu , Abhijit Biswas , Ajay Mittal , Aniruddha Mondal , Romanov Oleksandr Ivanovich
The combining microelectronic devices and associated technologies onto a single silicon chip poses a substantial challenge. However, in recent years, the area of silicon photonics has experienced remarkable advancements and notable leaps in performance. The performance of silicon on insulator (SOI) based photonic devices, such as fast silicon optical modulators, photonic transceivers, optical filters, etc., have been discussed. This would be a step forward in creating standalone silicon photonic devices, strengthening the possibility of single on-chip nanophotonic integrated circuits. Suppose an integrated silicon photonic chip is designed and fabricated. In that case, it might drastically modify these combined photonic component costs, power consumption, and size, bringing substantial, perhaps revolutionary, changes to the next-generation communications sector. Yet, the monolithic integration of photonic and electrical circuitry is a significant technological difficulty. A complicated set of factors must be carefully considered to determine which application will have the best chance of success employing silicon-based integrated product solutions. The processing limitations connected to the current process flow, the process generation (sometimes referred to as lithography node generation), and packaging requirements are a few of these factors to consider. This review highlights recent developments in integrated silicon photonic devices and their proven applications, including but not limited to photonic waveguides, photonic amplifiers and filters, on-chip photonic transceivers, and the state-of-the-art of silicon photonic in multidimensional quantum systems. The investigated devices aim to expedite the transfer of silicon photonics from academia to industry by opening the next phase in on-chip silicon photonics and enabling the application of silicon photonic-based devices in various optical systems.
将微电子器件和相关技术结合到单个硅芯片上提出了重大挑战。然而,近年来,硅光子学领域经历了显著的进步和显著的性能飞跃。讨论了基于绝缘体上硅(SOI)的光子器件的性能,如快速硅光调制器、光子收发器、光滤波器等。这将是制造独立硅光子器件的一个进步,增强了单片纳米光子集成电路的可能性。假设设计并制造了集成硅光子芯片。在这种情况下,它可能会彻底改变这些组合光子元件的成本、功耗和尺寸,给下一代通信领域带来实质性的、也许是革命性的变化。然而,光子和电路的单片集成是一个重大的技术难题。必须仔细考虑一系列复杂的因素,以确定采用硅基集成产品解决方案的应用程序最有可能成功。与当前工艺流程、工艺生成(有时称为光刻节点生成)和封装要求相关的工艺限制是需要考虑的几个因素。本文重点介绍了集成硅光子器件的最新发展及其成熟的应用,包括但不限于光子波导、光子放大器和滤波器、片上光子收发器以及多维量子系统中硅光子的最新技术。所研究的器件旨在通过打开片上硅光子学的下一阶段并使基于硅光子学的器件在各种光学系统中的应用,加速硅光子学从学术界向工业的转移。
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引用次数: 0
Ni–Zn bimetal-organic framework nanoprobes reinforced polymeric coating to achieve dual-responsive warning of coating damage and interfacial corrosion 镍锌双金属有机框架纳米探针加固聚合物涂层,实现涂层损伤和界面腐蚀双重响应预警
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-06-01 DOI: 10.1016/j.nanoms.2024.03.009
Dezhi Jiao , Chengbao Liu , Yujie Qiang , Shuoqi Li , Cong Sun , Peimin Hou , Lanyue Cui , Rongchang Zeng
Coating microdefects and localized corrosion in coating/metal system are inevitable, accelerating the degradation of metal infrastructure. Early evaluating coating microdefects and detecting corrosion sites are urgent yet remain challenge to achieve. Herein, we propose a robust, universal and efficient fluorescence-based strategy for hierarchical warning of coating damage and metal corrosion by introducing the concepts of damage-induced fluorescence enhancement effect (DIE) and ionic-recognition induced quenching effect (RIQ). The coatings with dual-responsiveness for coating defect and steel corrosion are constructed by incorporating synthesized nanoprobes composed of metal organic frameworks (Ni–Zn-MOFs) loaded with Rhodamine B (RhB@MOFs). The initial damage to the coating causes an immediate intensification of fluorescence, while the specific ionic-recognition characteristic of RhB with Fe3+ results in an evident fluorescence quenching, enabling the detection of coating damage and corrosion. Importantly, this nanoprobes are insensitive to the coating matrix and exhibit stable corrosion warning capability across various coating systems. Meanwhile, electrochemical investigations indicate that the impedance values of RM/EP maintain above 108 ​Ω ​cm2 even after 60 days of immersion. Therefore, the incorporation of fluorescent nanoprobes greatly inhibits the intrusion of electrolytes into polymer and improves the corrosion protection performance of the coating. This powerful strategy towards dual-level damage warning provides insights for the development of long-term smart protective materials.
涂层微缺陷和涂层/金属体系的局部腐蚀是不可避免的,加速了金属基础结构的退化。早期评估涂层微缺陷和检测腐蚀部位是目前迫切需要解决的问题。在此,我们通过引入损伤诱导荧光增强效应(DIE)和离子识别诱导猝灭效应(RIQ)的概念,提出了一种鲁棒、通用和高效的基于荧光的涂层损伤和金属腐蚀分层预警策略。采用负载罗丹明B (RhB@MOFs)的ni - zn - mof金属有机骨架(ni - zn - mof)合成纳米探针,构建了对涂层缺陷和钢腐蚀具有双重响应性的涂层。涂层的初始损伤导致荧光立即增强,而RhB与Fe3+的特定离子识别特性导致荧光明显猝灭,从而可以检测涂层的损伤和腐蚀。重要的是,这种纳米探针对涂层基体不敏感,并且在各种涂层系统中表现出稳定的腐蚀预警能力。同时,电化学研究表明,浸泡60天后,RM/EP的阻抗值仍保持在108 Ω cm2以上。因此,荧光纳米探针的加入极大地抑制了电解质对聚合物的侵入,提高了涂层的防腐性能。这种强大的双级损伤预警策略为长期智能防护材料的开发提供了见解。
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引用次数: 0
Synthesis of binary and ternary MOF/carbon based composites (MOF/carbon nitride/graphene oxide) for the visible-light assisted destruction of tetracycline and textile dye 合成二元和三元 MOF/碳基复合材料(MOF/氮化碳/氧化石墨烯),用于可见光辅助破坏四环素和纺织染料
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-06-01 DOI: 10.1016/j.nanoms.2024.04.015
Niyaz Mohammad Mahmoodi, Seyed Behnam Bagherzadeh
Herein, binary and ternary MOF/carbon based composites (MOF/Carbon nitride/Graphene oxide) (novel binary (NH2-MIL-88B(Fe)/g-C3N4) (MOF/Carbon nitride) and ternary (NH2-MIL-88B(Fe)/g-C3N4/GO) (MOF/Carbon nitride/Graphene oxide) composites) were synthesized and used as photocatalysts for the elimination of Direct Red 23 (D-Red23) and Tetracycline Hydrochloride (TC-H). NH2-MIL-88B(Fe)/g-C3N4/GO (MILB/g/GO) ternary composites with three different amounts of GO including 3, 7, and 11 ​wt% were synthesized and denoted as MILB/g/(3%)GO, MILB/g/(7%)GO, and MILB/g/(11%)GO. g-C3N4 and GO (with three different amounts 3, 7, and 11 ​wt%) were incorporated to synthesize MILB/g/(3%)GO, MILB/g/(7%)GO and MILB/g/(11%)GO ternary composites. Several analyses were used to characterize the materials. The MILB/g/(3%)GO demonstrated the highest pollutant degradation efficiency. The degradation rate of dye and Tetracycline after 70 ​min of light radiation using MILB/g/(3%)GO in a photo-Fenton-like reaction was about 99% and 96%, respectively. The creation of a heterojunction structure using g-C3N4, and the simultaneous incorporation of the optimum amount of GO led to a remarkable amelioration in photocatalytic properties and the extraordinary performance of MILB/g/(3%)GO in the pollutants degradation process.
本文合成了二元和三元MOF/碳基复合材料(MOF/氮化碳/氧化石墨烯)(新型二元(NH2-MIL-88B(Fe)/g-C3N4) (MOF/氮化碳)和三元(NH2-MIL-88B(Fe)/g-C3N4/GO) (MOF/氮化碳/氧化石墨烯)复合材料),并将其作为光催化剂用于直接红23 (D-Red23)和盐酸四环素(TC-H)的消除。合成了NH2-MIL-88B(Fe)/g- c3n4 /GO (MILB/g/GO)三元复合材料,其中氧化石墨烯的添加量为3、7和11wt %,分别表示为MILB/g/(3%)GO、MILB/g/(7%)GO和MILB/g/(11%)GO。g- c3n4和氧化石墨烯(3、7和11 wt%)分别合成了MILB/g/(3%)氧化石墨烯、MILB/g/(7%)氧化石墨烯和MILB/g/(11%)氧化石墨烯三元复合材料。用了几种分析方法来表征材料。MILB/g/(3%)GO的污染物降解效率最高。MILB/g/(3%)氧化石墨烯在光- fenton -like反应中对染料和四环素的降解率分别为99%和96%。利用g- c3n4建立异质结结构,同时加入最优量的氧化石墨烯,显著改善了光催化性能,并且在污染物降解过程中表现出非凡的MILB/g/(3%)氧化石墨烯。
{"title":"Synthesis of binary and ternary MOF/carbon based composites (MOF/carbon nitride/graphene oxide) for the visible-light assisted destruction of tetracycline and textile dye","authors":"Niyaz Mohammad Mahmoodi,&nbsp;Seyed Behnam Bagherzadeh","doi":"10.1016/j.nanoms.2024.04.015","DOIUrl":"10.1016/j.nanoms.2024.04.015","url":null,"abstract":"<div><div>Herein, binary and ternary MOF/carbon based composites (MOF/Carbon nitride/Graphene oxide) (novel binary (NH<sub>2</sub>-MIL-88B(Fe)/g-C<sub>3</sub>N<sub>4</sub>) (MOF/Carbon nitride) and ternary (NH<sub>2</sub>-MIL-88B(Fe)/g-C<sub>3</sub>N<sub>4</sub>/GO) (MOF/Carbon nitride/Graphene oxide) composites) were synthesized and used as photocatalysts for the elimination of Direct Red 23 (D-Red23) and Tetracycline Hydrochloride (TC-H). NH<sub>2</sub>-MIL-88B(Fe)/g-C<sub>3</sub>N<sub>4</sub>/GO (MILB/g/GO) ternary composites with three different amounts of GO including 3, 7, and 11 ​wt% were synthesized and denoted as MILB/g/(3%)GO, MILB/g/(7%)GO, and MILB/g/(11%)GO. g-C<sub>3</sub>N<sub>4</sub> and GO (with three different amounts 3, 7, and 11 ​wt%) were incorporated to synthesize MILB/g/(3%)GO, MILB/g/(7%)GO and MILB/g/(11%)GO ternary composites. Several analyses were used to characterize the materials. The MILB/g/(3%)GO demonstrated the highest pollutant degradation efficiency. The degradation rate of dye and Tetracycline after 70 ​min of light radiation using MILB/g/(3%)GO in a photo-Fenton-like reaction was about 99% and 96%, respectively. The creation of a heterojunction structure using g-C<sub>3</sub>N<sub>4</sub>, and the simultaneous incorporation of the optimum amount of GO led to a remarkable amelioration in photocatalytic properties and the extraordinary performance of MILB/g/(3%)GO in the pollutants degradation process.</div></div>","PeriodicalId":33573,"journal":{"name":"Nano Materials Science","volume":"7 3","pages":"Pages 359-376"},"PeriodicalIF":9.9,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141143083","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
Rational design of donor-acceptor structured tubular carbon nitride modulates charge distribution for photocatalytic hydrogen evolution 合理设计供体-受体结构管状氮化碳调节光催化析氢的电荷分布
IF 17.9 2区 材料科学 Q1 Engineering Pub Date : 2025-04-28 DOI: 10.1016/j.nanoms.2025.03.007
Qiuheng Wang , Guanyu Wu , Pengfei Zheng , Luye Pan , Zhao Mo , Peipei Sun , Xianglin Zhu , Yaqi Han , Songmei Wang , Hui Xu
Photocatalysis is one of the most promising technologies for solving environmental and energy problems, but current photocatalysts still suffer from low visible light utilization and insufficient photogenerated charge separation efficiency. Therefore, in this work, D-A tubular materials with tubular carbon nitride (TCN) as electron donor (D) and 2-mercaptobenzothiazole (BZ) as electron acceptor (A) were constructed by molecular doping and modulation of the carbon nitride geometry. It was shown that the introduction of BZ could modulate the electronic structure of the catalyst, promote electron migration from TCN to BZ, and inhibit the recombination of photogenerated electrons and holes. Meanwhile, the ultra-thin tubular structure could expose more active sites. In addition, the adsorption of protons by BZ-TCN was further improved due to the modulation of the charge distribution between the components by the introduction of small molecules. Among them, the photocatalytic hydrogen production rate of BZ0.1-TCN was twice that of TCN. The in-depth discussion of the components through theoretical calculations and characterization tests contributes to the understanding of the mechanism of photocatalytic hydrogen production.
光催化是解决环境和能源问题最有前途的技术之一,但目前光催化剂存在可见光利用率低、光电分离效率低等问题。因此,本文采用分子掺杂和氮化碳几何结构调制的方法,构建了以管状氮化碳(TCN)为电子给体(D)、2-巯基苯并噻唑(BZ)为电子受体(A)的D-A管状材料。结果表明,BZ的引入可以调节催化剂的电子结构,促进电子从TCN向BZ迁移,抑制光生电子与空穴的复合。同时,超薄管状结构可以暴露更多的活性位点。此外,BZ-TCN对质子的吸附性能由于引入小分子调控了组分间的电荷分布而进一步提高。其中,BZ0.1-TCN的光催化产氢速率是TCN的2倍。通过理论计算和表征试验对组分进行深入讨论,有助于理解光催化制氢的机理。
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引用次数: 0
Novel ternary Z scheme carbon quantum dots (CQDs) decorated WS2/PANI ((CQDs@WS2/PANI):0D:2D:1D) nanocomposite for the photocatalytic degradation and electrochemical detection of pharmaceutical drugs 用于药物光催化降解和电化学检测的新型三元 Z 方案碳量子点 (CQDs) 装饰 WS2/PANI ((CQDs@WS2/PANI):0D:2D:1D)纳米复合材料
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-04-01 DOI: 10.1016/j.nanoms.2024.04.005
Tarab Fatima, Samina Husain, Manika Khanuja
The endocrine-disrupting chemicals (EDCs) and antibiotics are causing negative effects on human beings and animals by disrupting the endocrine system and spreading antimicrobial resistance. The current need is to eradicate pharmaceutical waste from water bodies using advanced catalytic systems with high efficiency. Novel ternary carbon quantum dots (CQDs) decorated Z-Scheme WS2-PANI nanocomposite was prepared by a green synthesis assisted in-situ polymerization for the photodegradation and detection of Estradiol (EST) and Nitrofurantoin (NFT). HRTEM micrographs revealed the formation of CQDs with a mean size of 4 ​nm anchored on the surface of WS2/PANI (width:PANI ​∼ ​20–30 ​nm). The ternary nanocomposite showed excellent photocatalytic activity, degraded NFT (95.7 ​% in 60 ​min), and EST (96.6 ​% in 60 ​min). The rate kinetics study confirms the reaction followed pseudo first-order model. This heterostructure exhibited enhanced performances by modulating the energy level configuration, enhancing the absorption of visible light (2.4 ​eV), and significantly improving the charge separation, three times higher than pristine WS2. These are highly favorable for increasing the generation of photoinduced charges and enhancing the overall performance of the catalyst. Further, the electrochemical sensor was prepared using CQDs@WS2/PANI nanocomposite on a paper-based electrode. The CQDs@WS2/PANI exhibit a linear response of 0.1–100 ​nM, with a limit of detection of 13 ​nM. This synergistic interfacial interaction resulted in the significantly improved electrochemical performance of the modified electrode. The proposed Z-scheme was justified by electron paramagnetic resonance (EPR) and scavenger experiment. An intermediate degradation pathway was also proposed. The synthesized materials were characterized using FESEM, HRTEM, XRD, FTIR, XPS, UV-visible spectroscopy, PL, and TRPL. Therefore, this study provides a direct approach to fabricate a heterojunction that combines two-dimensional, one dimensional, and zero-dimensional properties, enabling control over the energy level configuration and subsequent improvements in photocatalytic and electrocatalytic efficiency.
内分泌干扰物(EDCs)和抗生素通过扰乱内分泌系统和传播抗菌素耐药性对人类和动物造成负面影响。目前的需求是利用先进的高效催化系统来清除水体中的药物废物。采用原位聚合辅助绿色合成法制备了新型三元碳量子点修饰的Z-Scheme WS2-PANI纳米复合材料,用于检测雌二醇(EST)和呋喃醌(NFT)。HRTEM显微照片显示,在WS2/PANI(宽度:PANI ~ 20-30 nm)表面形成了平均尺寸为4 nm的CQDs。该三元复合材料具有良好的光催化活性,60 min降解NFT (95.7%), 60 min降解EST(96.6%)。速率动力学研究证实该反应符合准一阶模型。该异质结构通过调制能级构型,增强了对可见光的吸收(2.4 eV),并显著提高了电荷分离度,比原始WS2提高了3倍。这对于增加光诱导电荷的产生和提高催化剂的整体性能是非常有利的。此外,在纸基电极上使用CQDs@WS2/聚苯胺纳米复合材料制备了电化学传感器。CQDs@WS2/PANI的线性响应范围为0.1 ~ 100 nM,检测限为13 nM。这种协同界面相互作用导致修饰电极的电化学性能显著提高。通过电子顺磁共振(EPR)和清道夫实验验证了该方案的正确性。提出了一种中间降解途径。采用FESEM、HRTEM、XRD、FTIR、XPS、uv -可见光谱、PL和TRPL对合成材料进行了表征。因此,本研究提供了一种直接的方法来制造结合二维、一维和零维性质的异质结,从而能够控制能级配置并随后提高光催化和电催化效率。
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引用次数: 0
Construction of gradient hierarchical and hetero-interfaces structure for ultra-broad microwave absorption 超宽微波吸收梯度分层异质界面结构的构建
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-04-01 DOI: 10.1016/j.nanoms.2024.04.004
Chunwei Lei , Jian Li , Yuhan Wu , Yu Xie , Yun Ling , Juhua Luo
Currently, carbon materials derived from biomass are widely sought after as electromagnetic absorbing(EMWA) materials owing to the unique structure, as well as the wide range of natural acquisition pathways, economic viability, and simple processing. However, due to the high dielectric properties, mismatched impedance and single attenuation mechanism, they cannot achieve efficient EMWA performance. Herein, the biomass carbon/Co/porous carbon magnetic composites with a layered gradient structure were fabricated by in-situ deposition of ZIF-67 on the lotus leaf base and then pyrolysis at high temperature. By adjusting the pyrolysis temperature, the sample obtained at 650 ​°C achieved a minimum reflection value (RLmin) of −34.2 ​dB at a matching thickness of 2.6 ​mm, and a maximum effective absorption bandwidth (EAB) of 7.12 ​GHz. The results indicate that this magnetic composite with a multi-sized layered gradient porous structure has a good electron transport network, a large number of heterogeneous interfaces, and dipole polarization centers, which are conducive to multiple reflection and scattering of microwaves, conduction loss, interface loss, magnetic loss, and impedance matching of materials. Therefore, this work provided a reference for optimizing the EMWA performance of carbon materials and designing a layered gradient porous magnetic composite with multi-sized structure.
目前,生物质碳材料因其结构独特、自然获取途径广泛、经济可行、加工简单等优点,作为电磁吸收(EMWA)材料受到广泛追捧。但由于介电性能高、阻抗不匹配、衰减机制单一,无法实现高效的EMWA性能。本文通过在荷叶基底上原位沉积ZIF-67,并进行高温热解,制备了具有层状梯度结构的生物质碳/Co/多孔碳磁性复合材料。通过调节热解温度,650℃下得到的样品在匹配厚度为2.6 mm时的最小反射值(RLmin)为−34.2 dB,最大有效吸收带宽(EAB)为7.12 GHz。结果表明,这种多层梯度多孔结构的磁性复合材料具有良好的电子输运网络、大量的非均相界面和偶极极化中心,有利于微波的多次反射和散射、导电损耗、界面损耗、磁损耗和材料的阻抗匹配。因此,本研究为优化碳材料的EMWA性能,设计多层梯度多孔磁性复合材料提供了参考。
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引用次数: 0
Borophene: A 2D wonder shaping the future of nanotechnology and materials science 硼菲:塑造纳米技术和材料科学未来的二维奇迹
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-04-01 DOI: 10.1016/j.nanoms.2024.03.007
Raghvendra Kumar Mishra , Jayati Sarkar , Kartikey Verma , Iva Chianella , Saurav Goel , Hamed Yazdani Nezhad
Two-dimensional (2D) materials have attracted considerable research interest due to their precisely defined properties and versatile applications. In this realm, borophene - a single atomic sheet of boron atoms arranged in a honeycomb lattice - has emerged as a promising candidate. While borophenes were theoretically predicted to have unique structural, optical, and electronic properties, the experimental synthesis of crystalline borophene sheets was first demonstrated on metal substrates in 2015, marking a crucial milestone. Since then, research efforts have focused on controlling the synthesis of semiconducting borophene polymorphs and exploring their novel physical characteristics. This review aims to explore the potential of 2D materials, specifically borophene, in various technological fields such as batteries, supercapacitors, fuel cells, and more. The analysis emphasises meticulous scrutiny of synthesis techniques due to their fundamental importance in realising borophene's properties. Specifically, the high carrier mobilities, tuneable bandgaps, and exceptional thermal conductivity of borophene are highlighted. By providing a comprehensive outlook on the significance of borophene in advancing materials science and technologies, this review contributes to shaping the landscape of 2D material research.
二维(2D)材料由于其精确定义的性质和广泛的应用而引起了相当大的研究兴趣。在这个领域,硼罗芬——一种排列成蜂窝状晶格的硼原子单原子片——已经成为一个很有希望的候选者。虽然理论上预测硼罗芬具有独特的结构、光学和电子特性,但2015年在金属衬底上首次展示了晶体硼罗芬片的实验合成,这是一个至关重要的里程碑。从那时起,研究工作集中在控制半导体硼罗芬多晶的合成和探索其新的物理特性。本文旨在探讨二维材料,特别是硼苯在电池、超级电容器、燃料电池等各个技术领域的潜力。分析强调了对合成技术的细致审查,因为它们在实现波罗芬的性质方面具有根本的重要性。特别地,高载流子迁移率,可调谐的带隙,以及波罗芬的特殊导热性被强调。通过对硼罗芬在推进材料科学和技术方面的意义进行全面的展望,本综述有助于塑造二维材料研究的景观。
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引用次数: 0
Facile and adjustable production of self–standing oxygen–doped graphene membranes for optimized oxygen evolution electrocatalysis 为优化氧进化电催化而方便、可调地生产自立式掺氧石墨烯膜
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2025-04-01 DOI: 10.1016/j.nanoms.2024.03.003
Liang Chen , Lanyun Yang , Liying Hu , Minghao Jin , Chenxi Xu , Binhong He , Wei Wang , Ying Liu , Gangyong Li , Zhaohui Hou
Owing to abundant resource and affordable price, metal–free carbon has been extensively studied in the field of oxygen reduction reaction, while the related studies on oxygen evolution reaction (OER) are quite few. In this work, a facile and scalable knife coating coupled with annealing strategy is proposed to produce self–standing oxygen–doped graphene membranes (marked as O–GM–T, T represents the annealing temperature). Through systematic characterization and analysis, it is discovered the annealing treatment not only decreases the amount of oxygenic groups, but allows for controlled regulation of the oxygen configurations, leaving only C–OH/C–O–C and CO. Meanwhile, theoretical calculations indicate that the OER activity trend of different oxygen configurations is as follows: –COOH ​> ​CO ​≈ ​C–OH ​> ​C–O–C. Despite the removal of highly active –COOH group through annealing treatment, the resulting O–GM–800 sample maintains good mechanical property and achieves a favorable balance on conductivity, hydrophilicity and catalytic sites. Consequently, it displays significantly improved OER performance compared to the counterparts, making it highly promising for applications in overall water splitting devices. Apparently, our work provides guidance for the rational design and controllable fabrication of self–standing carbon–based catalysts for energy–related reactions.
由于资源丰富、价格实惠,无金属碳在氧还原反应领域得到了广泛的研究,而在析氧反应(OER)方面的相关研究却很少。在这项工作中,提出了一种简单可扩展的刀涂结合退火策略来生产自给式掺氧石墨烯膜(标记为O-GM-T, T代表退火温度)。通过系统的表征和分析,发现退火处理不仅减少了含氧基团的数量,而且可以对氧构型进行可控调节,只留下C-OH / C-O-C和CO。同时,理论计算表明,不同氧构型的OER活度趋势如下:-COOH >;CO≈C-OH >;C-O-C。尽管通过退火处理去除了高活性的-COOH基团,但得到的O-GM-800样品保持了良好的力学性能,并在电导率、亲水性和催化位点上取得了良好的平衡。因此,与同类产品相比,它显示出显着改善的OER性能,使其在整体水分解装置中的应用具有很大的前景。显然,我们的工作为合理设计和可控制造用于能源相关反应的自立型碳基催化剂提供了指导。
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Nano Materials Science
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