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Strain promoted azide alkyne cycloaddition, an efficient surface functionalization strategy for microRNA magnetic separation 应变促进叠氮炔烃环化--一种用于 microRNA 磁分离的高效表面功能化策略
Pub Date : 2024-11-07 DOI: 10.1016/j.nxmate.2024.100409
Djamila Kechkeche , Sirine El Mousli , Claire Poujouly , Emilie Secret , Vincent Dupuis , Isabelle Le Potier , Marie-Emmanuelle Goriot , Julien Siracusa , Sébastien Banzet , Jean Gamby , Jean-Michel Siaugue
In an emergency context, the detection of microRNA (miRNA), which are potential biomarkers of cardiovascular and muscular pathologies is hampered by the time required for the various steps involved: treatment of the patient sample, reverse transcription (RT), and finally polymerase chain reaction (PCR). In this context, magnetically assisted extraction of miRNA could shorten the sample treatment duration and enable a potential pre-concentration to gain in sensitivity. To this goal, magnetic nanoparticles (MNP) functionalized with DNA were developed. Maghemite nanoparticles were coated with a layer of silica, doubly functionalized with PEG chains to guarantee colloidal stability and limit non-specific protein adsorption, and amine functions to allow post-functionalization with DNA which have complementary sequences of the targeted miRNA. Two post-functionalization strategies were tested, one based on the reaction between a thiolated DNA and a maleimide group at the surface of the MNP, the other between an azide-functionalized DNA and a dibenzocyclooctyne group on the surface of the MNP. The strain-promoted azide alkyne cycloaddition (SPAAC click chemistry) proved to be the most efficient functionalization strategy. Optimization of the complementary DNA grafting protocol, carried out by varying the ratios between the quantities of dibenzocyclooctyne groups and DNA and between the quantities of DNA and MNP, revealed on the one hand that the quantity of DNA grafted per nanoparticle could be finely controlled, and on the other hand that the grafting on the MNP’s surface of an excessive quantity of dibenzocyclooctyne groups led to a reduction in grafting yields. The optimized process was used for grafting the complementary DNA of 6 different miRNA, including 4 biomarkers of muscle injury (miR-1, 133a, 133b, and 206). It led to the grafting of approximately 4 complementary DNA per MNP, whatever the nucleotide sequence considered. Capture of the targeted miRNA by magnetic separation was then studied in buffered model media and in complex biological media. This study showed that MNP allowed magnetically-assisted extraction of target miRNA with good hybridization yields, even in biological media for which the capture capacity was preserved at around 75 %, with rapid kinetics and satisfactory selectivity.
微 RNA(miRNA)是心血管和肌肉病变的潜在生物标志物,在紧急情况下,检测微 RNA(miRNA)会受到各种步骤所需时间的影响:病人样本处理、反转录(RT)以及最后的聚合酶链反应(PCR)。在这种情况下,磁性辅助提取 miRNA 可以缩短样本处理时间,并实现潜在的预浓缩以提高灵敏度。为此,我们开发了 DNA 功能化的磁性纳米颗粒(MNP)。磁性纳米粒子表面涂有一层二氧化硅,并用 PEG 链进行了双重功能化处理,以保证胶体稳定性并限制非特异性蛋白质吸附,同时还添加了胺功能,以便与具有目标 miRNA 互补序列的 DNA 进行后功能化处理。我们测试了两种后功能化策略,一种是硫醇化 DNA 与 MNP 表面的马来酰亚胺基团发生反应,另一种是叠氮功能化 DNA 与 MNP 表面的二苯并环辛炔基团发生反应。应变促进叠氮炔烃环加成(SPAAC 点击化学)被证明是最有效的功能化策略。通过改变二苯并环辛炔基团和 DNA 数量之间的比例以及 DNA 和 MNP 数量之间的比例,对互补 DNA 接枝方案进行了优化,结果表明,一方面可以精细控制每个纳米粒子接枝 DNA 的数量,另一方面,在 MNP 表面接枝过量的二苯并环辛炔基团会降低接枝产量。优化后的工艺用于嫁接 6 种不同 miRNA 的互补 DNA,包括 4 种肌肉损伤生物标志物(miR-1、133a、133b 和 206)。无论核苷酸序列如何,每个 MNP 都能嫁接约 4 个互补 DNA。然后在缓冲模型介质和复杂生物介质中研究了通过磁分离捕获目标 miRNA 的情况。研究结果表明,MNP 可以在磁力辅助下提取目标 miRNA,杂交产量很高,即使在生物介质中,捕获能力也能保持在 75% 左右,并且具有快速的动力学和令人满意的选择性。
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引用次数: 0
Enhanced functionalities in flexible poly (vinylidene fluoride-trifluoroethylene)/cerium oxide doped sodium bismuth titanate [P(VDF-TrFE)/NBT-CeO2] ceramic polymer composite films: A comprehensive investigation of piezoelectric, pyroelectric, and ferroelectric properties 增强柔性聚(偏氟乙烯-三氟乙烯)/氧化铈掺杂钛酸铋钠 [P(VDF-TrFE)/NBT-CeO2] 陶瓷聚合物复合薄膜的功能:压电、热释电和铁电特性的综合研究
Pub Date : 2024-11-06 DOI: 10.1016/j.nxmate.2024.100416
T.S. Velayutham, N.A. Halim, W.H. Abd. Majid
In the pursuit of innovative smart polymer piezoelectric ceramic composites, we present a thorough examination of the physical, structural, and polarization characteristics of a novel flexible polymer ceramic composite comprising sodium-bismuth titanate (NBT) doped with 0.6 mass % CeO2 as ceramic fillers embedded in a poly (vinylidene fluoride-trifluoroethylene) (P(VDF-TrFE)) polymer matrix. The incorporation of these fillers serves to increase both the mechanical strength and functional attributes of the resulting polymer-ceramic composites. Various volume percentages of ceramic fillers were employed, and the experimental effective dielectric permittivity results were systematically fitted to established theoretical models, including Maxwell, ClausiusMossotti, Furukawa, and effective medium theory (EMT). Our findings reveal that the composite films exhibit exceptional piezo-, pyro-, and ferroelectric properties when compared to the pristine P(VDF-TrFE) copolymer. The optimum concentration of NBT-0.6 CeO2 filler was determined to be 0.2 vol fraction resulting in a remarkable enhancement of the key parameters. Specifically, the pyroelectric coefficient increased from 32 μC/m2K to 43 μC/m2K (a ∼35 % increment), remnant polarization surged from 80 mC/m2 to 166 mC/m2 (an impressive ∼110 % increment), and the piezoelectric constant (d33) elevated from −38 pC/N to 49 pC/N (a substantial ∼30 % increment). These findings signify the potential of these optimized samples for applications in high energy density capacitors and/or highly integrated and intelligent piezoelectric devices. This comprehensive investigation not only advances our understanding of the synergistic effects within polymer-ceramic composites but also underscores the potential of the proposed material system for practical applications, providing valuable insights for the development of advanced multifunctional materials.
为了开发创新型智能聚合物压电陶瓷复合材料,我们对一种新型柔性聚合物陶瓷复合材料的物理、结构和极化特性进行了深入研究,该复合材料由掺有 0.6 质量% CeO2 的钛酸铋钠 (NBT) 作为陶瓷填料嵌入聚偏氟乙烯-三氟乙烯 (P(VDF-TrFE)) 聚合物基体中组成。这些填料的加入可提高聚合物-陶瓷复合材料的机械强度和功能属性。我们采用了不同体积百分比的陶瓷填料,并将有效介电常数的实验结果系统地拟合到已建立的理论模型中,包括麦克斯韦理论、克劳修斯-莫索蒂理论、古河理论和有效介质理论(EMT)。我们的研究结果表明,与原始的 P(VDF-TrFE)共聚物相比,复合薄膜具有优异的压电、热释电和铁电特性。NBT-0.6 CeO2 填料的最佳浓度被确定为 0.2 体积分数,从而显著提高了关键参数。具体而言,热释电系数从 32 μC/m2K 增加到 43 μC/m2K(增加了 35%),残余极化从 80 mC/m2 激增到 166 mC/m2(显著增加了 110%),压电常数 (d33) 从 -38 pC/N 增加到 49 pC/N(大幅增加了 30%)。这些发现表明,这些优化样品具有应用于高能量密度电容器和/或高度集成的智能压电器件的潜力。这项全面的研究不仅加深了我们对聚合物陶瓷复合材料内部协同效应的理解,还强调了拟议材料系统在实际应用中的潜力,为先进多功能材料的开发提供了宝贵的见解。
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引用次数: 0
Harnessing machine learning for high-throughput screening of high thermal conductivity polyimides: A multiscale feature engineering approach 利用机器学习进行高热导率聚酰亚胺的高通量筛选:多尺度特征工程方法
Pub Date : 2024-11-06 DOI: 10.1016/j.nxmate.2024.100420
Jiale Han , Chunhua Ying , Yue Cao, Wen Li, Yuan Feng, Masood Mortazavi, Pingfan Wu, Liang Peng, Jiechen Wang
Polyimides are known for their exceptional thermal stability and are widely utilized in high-temperature and electronic applications. To further explore and broaden their application in electronic packaging and thermal management, developing polyimide with high thermal conductivity remains a significant challenge. In this study, we present a machine learning technique with novel multiscale feature engineering approach to predict and identify high thermal conductivity polyimide efficiently. Our workflow involves digitally representing chemical structures using physical insights and refining these representations through the Statistical – Tree – Recursive feature engineering pipeline, which includes three steps--statistical selection, tree-based cascading feature selection, and recursive feature elimination. This process results in the creation of a comprehensive combinational feature set. Multiple machine learning models were trained and validated, demonstrating high predictive accuracy and generalizability. High-throughput screening identified polyimide candidates with thermal conductivity values exceeding 0.4 W/(m⋅K), and these predictions were validated using non-equilibrium molecular dynamics simulation. This workflow provides valuable insights into structure-property relationships, offering a robust framework for designing polymer materials with improved thermal properties for applications in electronics packaging, flexible sensors, and other high-performance devices.
聚酰亚胺以其优异的热稳定性而著称,并广泛应用于高温和电子领域。为了进一步探索和拓宽聚酰亚胺在电子封装和热管理方面的应用,开发具有高热导率的聚酰亚胺仍然是一项重大挑战。在本研究中,我们提出了一种机器学习技术和新颖的多尺度特征工程方法,以有效预测和识别高导热性聚酰亚胺。我们的工作流程包括利用物理洞察力对化学结构进行数字化表示,并通过统计-树-递归特征工程管道完善这些表示,其中包括三个步骤--统计选择、基于树的级联特征选择和递归特征消除。这一过程的结果是创建了一个全面的组合特征集。多个机器学习模型经过训练和验证,显示出较高的预测准确性和通用性。高通量筛选确定了热导率值超过 0.4 W/(m⋅K) 的聚酰亚胺候选材料,并通过非平衡分子动力学模拟验证了这些预测结果。该工作流程提供了有关结构-性能关系的宝贵见解,为设计具有更好热性能的聚合物材料提供了一个稳健的框架,这些材料可应用于电子封装、柔性传感器和其他高性能设备。
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引用次数: 0
Extraction and characteristic properties analyses of sodium alginate derived from the Sargassum oligocystum brown seaweed alga of the Bay of Bengal 从孟加拉湾马尾藻提取的海藻酸钠及其特性分析
Pub Date : 2024-11-05 DOI: 10.1016/j.nxmate.2024.100417
Md. Anwar Arfien Khan , Md. Monjurul Hasan , Md. Kawsar Hossain , Dabashes Adhikery , Mahmuda Hakim , Liton Chandra Mohanta , Abu Sayeed Muhammed Sharif , Ashish Kumar Sarker
Sodium alginate extracted from Sargassum oligocystum brown seaweed alga is an important blue economy development process of the Bay of Bengal. In the present study, sodium alginate was extracted from the brown seaweed alga collected from the Cox’s Bazar coastal area of the Bay of Bengal. The extracted product was characterized with the Ultraviolet-visible (UV–visible) spectrophotometer, Fluorescence spectrophotometer, Fourier transform-infrared radiation (FT-IR) spectrophotometer, X-ray diffractometer (XRD), and Scanning electron microscope (SEM). The product yield was optimized with different pH levels and the maximum yield was obtained at 32.5 % at pH 10.96. The moisture, and ash content of the extracted product was measured and found at 13.25 % and 4.35 %, respectively. The viscosity of the extracted product was obtained at 60.1 mPs. The UV–visible spectrophotometry showed different absorbance peaks found at 234 nm, 240 nm, 250 nm, and 264 nm which assigned the extracted product of sodium alginate, and the maximum absorption peak lies at 276.7 nm which assigned flavonoids, and their derivatives of alginates. The fluorescence spectrophotometry demonstrated a strong emission peak at 460 nm with higher intensity (200), indicating the presence of sodium alginate. The FTIR showed the characteristic peaks that demonstrated different functional groups of sodium alginate. The XRD pattern demonstrated 0.24 crystalline indexes indicating the semi-crystalline product in nature. SEM showed clear fibrils of sodium alginate morphology indicating the absence of impurity materials.
从马尾藻(Sargassum oligocystum)褐海藻中提取海藻酸钠是孟加拉湾蓝色经济发展过程中的一项重要内容。本研究从孟加拉湾考克斯巴扎尔沿海地区采集的褐藻中提取了海藻酸钠。使用紫外可见分光光度计、荧光分光光度计、傅立叶变换红外分光光度计、X 射线衍射仪和扫描电子显微镜对提取的产品进行了表征。根据不同的 pH 值对产品收率进行了优化,pH 值为 10.96 时收率最高,为 32.5%。经测量,提取物的水分和灰分含量分别为 13.25 % 和 4.35 %。提取物的粘度为 60.1 mPs。紫外-可见分光光度法在 234 nm、240 nm、250 nm 和 264 nm 处发现了不同的吸光度峰,这些吸光度峰代表了海藻酸钠提取物,最大吸光度峰位于 276.7 nm 处,代表了黄酮类化合物及其海藻酸盐衍生物。荧光分光光度法显示,在 460 纳米处有一个强度较高(200)的强烈发射峰,表明存在海藻酸钠。傅立叶变换红外光谱显示了海藻酸钠不同官能团的特征峰。X 射线衍射图显示结晶指数为 0.24,表明产品性质为半结晶。扫描电子显微镜(SEM)显示了清晰的海藻酸钠纤维形态,表明其中不含杂质。
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引用次数: 0
In situ formation of oxygen-deficient WO3-x nanosheets for enhanced photocatalytic activity in water splitting and plastic reforming 原位形成缺氧 WO3-x 纳米片,增强水分离和塑料重整中的光催化活性
Pub Date : 2024-11-05 DOI: 10.1016/j.nxmate.2024.100421
Yangsen Xu , Wenwu Shi , Biao Huang , Shuang Tang , Zhenyuan Jin , Yonghao Xiao , Feifei Lu , Xinzhong Wang
Photocatalytic pathways are essential for the sustainable production of chemicals and fuels, pivotal for achieving a pollution-free planet. Electron-hole recombination is a critical problem that has, so far, limited the efficiency of the photocatalytic materials. Here, oxygen-deficient WO3-x nanosheets were in situ grown in a polymeric carbon nitride (PCN) support during the thermal polycondensation of melamine. The introduction of defect in WO3-x, accompanied by spin polarization and the formed WO3-x/PCN heterostructure, greatly accelerated the charge separation and transfer. The synthesized WO3-x/PCN composite exhibited a tenfold increase in hydrogen generation activity than pure PCN under visible-light (420 ≤ λ ≤ 780 nm). The WO3-x/PCN also demonstrated consecutive 24 h and stable photocatalytic H2 production in the aqueous plastic-containing [poly(vinyl alcohol) (PVA), poly(ethylene terephthalate) (PET) and the PET bottle] solutions under visible light. The hydrogen production rates were determined to be 111.2, 50.5, and 7.8 μmol·h−1·g−1 in PVA, PET and PET bottle, respectively. In addition, the oxygen vacancies WO3 with their localized surface plasmon resonance effect, facilitated efficient utilization of NIR photon and the hydrogen evolution rate over WO3-x/PCN reached to 120 μmol h−1·g−1 under NIR light (700 ≤ λ ≤ 780 nm). This research not only advances the potential applications of WO3-x/PCN in sustainable energy production but also provides insights into environmental remediation through the conversion of plastic wastes.
光催化途径对于化学品和燃料的可持续生产至关重要,是实现无污染地球的关键。迄今为止,电子-空穴重组是限制光催化材料效率的一个关键问题。在这里,三聚氰胺热缩聚过程中,缺氧的 WO3-x 纳米片被原位生长在聚合氮化碳(PCN)载体中。WO3-x 中缺陷的引入,伴随着自旋极化和形成的 WO3-x/PCN 异质结构,大大加速了电荷分离和转移。在可见光(420 ≤ λ ≤ 780 纳米)下,合成的 WO3-x/PCN 复合材料的制氢活性比纯 PCN 提高了十倍。在可见光下,WO3-x/PCN 还能在含塑料[聚乙烯醇(PVA)、聚对苯二甲酸乙二醇酯(PET)和 PET 瓶]的水溶液中连续 24 小时稳定地光催化产生氢气。经测定,PVA、PET 和 PET 瓶的产氢率分别为 111.2、50.5 和 7.8 μmol-h-1-g-1。此外,氧空位 WO3 的局部表面等离子体共振效应促进了近红外光子的有效利用,在近红外光(700 ≤λ ≤ 780 nm)下,WO3-x/PCN 的氢进化率达到 120 μmol h-1-g-1。这项研究不仅推动了 WO3-x/PCN 在可持续能源生产中的潜在应用,还为通过转化塑料废弃物进行环境修复提供了启示。
{"title":"In situ formation of oxygen-deficient WO3-x nanosheets for enhanced photocatalytic activity in water splitting and plastic reforming","authors":"Yangsen Xu ,&nbsp;Wenwu Shi ,&nbsp;Biao Huang ,&nbsp;Shuang Tang ,&nbsp;Zhenyuan Jin ,&nbsp;Yonghao Xiao ,&nbsp;Feifei Lu ,&nbsp;Xinzhong Wang","doi":"10.1016/j.nxmate.2024.100421","DOIUrl":"10.1016/j.nxmate.2024.100421","url":null,"abstract":"<div><div>Photocatalytic pathways are essential for the sustainable production of chemicals and fuels, pivotal for achieving a pollution-free planet. Electron-hole recombination is a critical problem that has, so far, limited the efficiency of the photocatalytic materials. Here, oxygen-deficient WO<sub>3-x</sub> nanosheets were <em>in situ</em> grown in a polymeric carbon nitride (PCN) support during the thermal polycondensation of melamine. The introduction of defect in WO<sub>3-x</sub>, accompanied by spin polarization and the formed WO<sub>3-x</sub>/PCN heterostructure, greatly accelerated the charge separation and transfer. The synthesized WO<sub>3-x</sub>/PCN composite exhibited a tenfold increase in hydrogen generation activity than pure PCN under visible-light (420 ≤ λ ≤ 780 nm). The WO<sub>3-x</sub>/PCN also demonstrated consecutive 24 h and stable photocatalytic H<sub>2</sub> production in the aqueous plastic-containing [poly(vinyl alcohol) (PVA), poly(ethylene terephthalate) (PET) and the PET bottle] solutions under visible light. The hydrogen production rates were determined to be 111.2, 50.5, and 7.8 μmol·h<sup>−1</sup>·g<sup>−1</sup> in PVA, PET and PET bottle, respectively. In addition, the oxygen vacancies WO<sub>3</sub> with their localized surface plasmon resonance effect, facilitated efficient utilization of NIR photon and the hydrogen evolution rate over WO<sub>3-x</sub>/PCN reached to 120 μmol h<sup>−1</sup>·g<sup>−1</sup> under NIR light (700 ≤ λ ≤ 780 nm). This research not only advances the potential applications of WO<sub>3-x</sub>/PCN in sustainable energy production but also provides insights into environmental remediation through the conversion of plastic wastes.</div></div>","PeriodicalId":100958,"journal":{"name":"Next Materials","volume":"6 ","pages":"Article 100421"},"PeriodicalIF":0.0,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142586571","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single atom Pt supported by two-dimensional transition metal dichalcogenides for photocatalytic removal of harmful gases: A density functional theory study 二维过渡金属二卤化物支撑的单原子铂用于光催化去除有害气体:密度泛函理论研究
Pub Date : 2024-11-04 DOI: 10.1016/j.nxmate.2024.100418
Wentao Zhang , Degui Gao , Yue Zhao , Zhifeng Li , Wenguang Huang , Tianyin Huang , Bingdang Wu
Two-dimensional transition metal dichalcogenides (TMDs) has a broad application prospect in photocatalytic removal of harmful gases, but it is limited by the slow carrier separation efficiency. In order to improve the slow carrier dynamics, loading the TMDs with trace precious metals is an effective strategy. Thanks to the presence of precious metals, the recombination of electron and hole is inhibited. In this paper, the photocatalytic removal potential of single atom Pt supported by TMDs for harmful gases was discussed. Specifically, using density functional theory, it was found that Pt@2H-MoS2 and Pt@2H-MoSe2 possessed moderate bandgap widths, excellent stability and light absorption ability. Using CO, NO, SO and SO2 as model harmful gases, it was proved that Pt@2H-MoS2 and Pt@2H-MoSe2 can realize the photocatalytic removal of harmful gases by charge transfer and molecular orbital hybridization analysis. The above calculations exhibit that Pt@2H-MoS2 and Pt@2H-MoSe2 photocatalysts with excellent activity and stability possess broad prospects for the removal of harmful gases.
二维过渡金属二钙化物(TMDs)在光催化去除有害气体方面具有广阔的应用前景,但它受限于缓慢的载流子分离效率。为了改善缓慢的载流子动力学,在 TMDs 中添加痕量贵金属是一种有效的策略。由于贵金属的存在,电子和空穴的重组受到抑制。本文讨论了 TMD 支持的单原子铂对有害气体的光催化去除潜力。具体而言,利用密度泛函理论发现 Pt@2H-MoS2 和 Pt@2H-MoSe2 具有适中的带隙宽度、优异的稳定性和光吸收能力。以 CO、NO、SO 和 SO2 为模型有害气体,通过电荷转移和分子轨道杂化分析,证明了 Pt@2H-MoS2 和 Pt@2H-MoSe2 能够实现对有害气体的光催化去除。上述计算结果表明,Pt@2H-MoS2 和 Pt@2H-MoSe2 光催化剂具有优异的活性和稳定性,在去除有害气体方面具有广阔的应用前景。
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引用次数: 0
Nanoparticle integrated guar gum hydrogel-based immunosensor for biomedical application 用于生物医学应用的纳米粒子集成瓜尔胶水凝胶免疫传感器
Pub Date : 2024-11-04 DOI: 10.1016/j.nxmate.2024.100407
Shweta Panwar , Suveen Kumar
This paper contains results of studies related to fabrication of nanostructured metal oxide (MO) doped guar gum hydrogel (GGH) based immunosensing platform for detection of oral cancer biomarker (CYFRA-21–1). First, we synthesized nanostructured zirconia (nZrO2) through hydrothermal process and thereafter it has been functionalized with serine amino acid. The GGH has been synthesized through chemical process. Further, the solution of nZrO2 was mixed with GGH in 1:1 ratio in ddH2O. The prepared mixture has been further deposited onto a pre-hydrolyzed indium oxide (ITO) coated glass electrode through drop cast method. The anti-CYFRA-21–1 has been immobilized through EDC-NHS chemistry and Bovine Serum Albumin (BSA) has been used for blocking of nonspecific binding sites. X-Ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR) have been used to investigate morphological as well as functional characterization of synthesized material. However, electrochemical studies have been used to characterize fabricated electrodes as well as response studies. The fabricated immunoelectrode (BSA/anti-CYFRA-21–1/Serine/nZrO2/Hydrogel/ITO) exhibits a wider linear detection range (2.5–80 ng mL−1), remarkably high sensitivity (0.86 µA mg−1 mL cm−2) with shelf life up to 48 days. The electrochemical response studies of fabricated electrode have been further validated through enzyme-linked immunosorbent assay (ELISA) on to obtained saliva sample of oral cancer patients. Oral cancer biomarker detection is key for early diagnosis, personalized treatment, monitoring, enabling timely interventions and improved patient outcomes. We can easily investigate the stage of oral cancer through the detection of concentration of biomarkers secreted in saliva sample of oral cancer patients.
本文介绍了基于掺杂瓜尔胶水凝胶(GGH)的纳米结构金属氧化物(MO)免疫传感平台的研究成果,该平台用于检测口腔癌生物标记物(CYFRA-21-1)。首先,我们通过水热法合成了纳米氧化锆(nZrO2),然后用丝氨酸对其进行了功能化。GGH 是通过化学工艺合成的。然后,在 ddH2O 中以 1:1 的比例将 nZrO2 溶液与 GGH 混合。制备好的混合物通过滴注法进一步沉积在预水解氧化铟(ITO)涂层玻璃电极上。抗 CYFRA-21-1 通过 EDC-NHS 化学方法固定,牛血清白蛋白(BSA)用于阻断非特异性结合位点。X 射线衍射 (XRD)、扫描电子显微镜 (SEM)、透射电子显微镜 (TEM) 和傅立叶变换红外光谱 (FTIR) 被用来研究合成材料的形态和功能特征。然而,电化学研究已被用于表征制备的电极以及反应研究。制备的免疫电极(BSA/抗-CYFRA-21-1/丝氨酸/nZrO2/水凝胶/ITO)具有更宽的线性检测范围(2.5-80 ng mL-1)、极高的灵敏度(0.86 µA mg-1 mL cm-2)和长达 48 天的保质期。通过对口腔癌患者唾液样本进行酶联免疫吸附试验(ELISA),进一步验证了制备电极的电化学响应研究。口腔癌生物标志物检测是早期诊断、个性化治疗、监测、及时干预和改善患者预后的关键。通过检测口腔癌患者唾液样本中分泌的生物标志物的浓度,我们可以轻松了解口腔癌的分期。
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引用次数: 0
Deep learning based segmentation of binder and fibers in gas diffusion layers 基于深度学习的气体扩散层中粘合剂和纤维的分割
Pub Date : 2024-10-31 DOI: 10.1016/j.nxmate.2024.100411
Andreas Grießer , Rolf Westerteiger , Erik Glatt , Hans Hagen , Andreas Wiegmann
Gas diffusion layers (GDLs) are vital parts for the performance of proton-exchange membrane fuel cells (PEMFCs). In many cases, they are made of Carbon-Carbon Composite Paper (CCCP), which consists of carbon fibers and a carbonized binder material. The distribution of the fibers and binder in the GDL strongly influences the performance of a PEMFC. Synchrotron scans are a great way to obtain information about the microstructural composition of carbon paper GDLs (Figure 2), but there is one major obstacle. Binder and fibers tend to have the same attenuation and, consequently, the same gray values in the scans. To overcome this, we introduce a machine learning-based method that segments fibers and binder from the local morphology of a CCCP. The training data is generated using FiberGeo, a module in the GeoDict software for fibrous microstructure generation. FiberGeo creates fibers based on stochastic geometry and adds binder using morphological opening and closing operations. We applied the machine learning-based method to four Scans of samples of Toray Carbon Paper with varying amounts of binder in them. The result is the quantification of individual voxels as fiber or binder material that can be used, for example, in performance simulations of property simulations in PEMFCs [1], [2], [3], [4]. Here, we focus on the differences in the spatial distribution of the binder both in the through-plane and in-plane directions.
气体扩散层(GDL)是质子交换膜燃料电池(PEMFC)性能的重要组成部分。在许多情况下,它们由碳碳复合纸(CCCP)制成,后者由碳纤维和碳化粘合剂材料组成。纤维和粘合剂在 GDL 中的分布对 PEMFC 的性能有很大影响。同步辐射扫描是获得碳纸 GDL 微结构组成信息的重要途径(图 2),但存在一个主要障碍。粘合剂和纤维往往具有相同的衰减,因此扫描中的灰度值也相同。为了克服这一问题,我们引入了一种基于机器学习的方法,该方法可根据 CCCP 的局部形态来分割纤维和粘合剂。训练数据通过 FiberGeo 生成,FiberGeo 是 GeoDict 软件中用于生成纤维微结构的一个模块。FiberGeo 根据随机几何形状创建纤维,并通过形态学开合操作添加粘结剂。我们将基于机器学习的方法应用于东丽碳纸样品的四次扫描,其中含有不同数量的粘合剂。其结果是将单个体素量化为纤维或粘合剂材料,例如,可用于 PEMFC 性能模拟和特性模拟 [1]、[2]、[3]、[4]。在此,我们将重点关注粘结剂在通面和面内两个方向上的空间分布差异。
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引用次数: 0
Effects of nickel-deactivations on zeolites-Y of different SiO2/Al2O3 ratios in catalytic cracking of hydrocarbons 镍失活对不同 SiO2/Al2O3 比率的沸石-Y 在催化裂解碳氢化合物中的影响
Pub Date : 2024-10-30 DOI: 10.1016/j.nxmate.2024.100413
D.E. Adanenche , A.Y. Atta , A. Aliyu , B.J. El-Yakubu
Effects of nickel deactivation on catalytic activities of three types of zeolites-Y (Y-5.1, USY-5.2, and VUSY-12) with varying SiO2/Al2O3 ratios were studied in cracking of hydrocarbons. Physicochemical characteristics such as crystalline phases, Ni oxidation states, morphology, acidity, surface area, and thermal stability of the samples were analysed. XRD revealed the absence of observable nickel compounds below 5 wt%, with NiO phase emerging at higher concentrations. Surface areas decreased from 826 to 615 m2/g (Y-5.1), 786–686 m2/g (USY-5.2), and 762–571 m2/g (VUSY-12) at 30 wt% Ni. The total acid sites also reduced from 17.247 to 9.826 µmol/g (Y-5.1), 15.464–8.854 µmol/g (USY-5.2), and 7.094–4.876 µmol/g (VUSY-12). XPS confirmed Ni2+ states. Catalytic cracking tests using n-Heptane demonstrated increases in C5-C6 alkanes, olefins, hydrogen, and methane yields as nickel concentration increased, with respective values of 64 %, 28 %, 79 % and 68 % for Y-5.1; 62 %, 28 %, 76 %, and 62 % for USY-5.2; and 58 %, 21 %, 75 %, and 60 % for VUSY-12. A corresponding decrease in heavier components were observed. The study demonstrates that nickel modification significantly impacts the physicochemical properties and catalytic performance of zeolite-Y and these depend strongly on the SiO2/Al2O3 ratios. The study gives further insights into the structural and catalytic modifications induced by nickel doping in zeolites, highlighting the potential of nickel-modified zeolites in promoting undesirable hydrogen and gas.
研究了镍失活对三种不同 SiO2/Al2O3 比率的沸石-Y(Y-5.1、USY-5.2 和 VUSY-12)在碳氢化合物裂解中催化活性的影响。对样品的结晶相、镍氧化态、形态、酸度、表面积和热稳定性等理化特性进行了分析。XRD 显示,5 wt% 以下的样品中没有可观察到的镍化合物,浓度越高,镍氧化物相越多。镍含量为 30 wt% 时,表面积从 826 m2/g 降至 615 m2/g(Y-5.1)、786-686 m2/g(USY-5.2)和 762-571 m2/g(VUSY-12)。总酸位点也从 17.247 微摩尔/克(Y-5.1)、15.464-8.854 微摩尔/克(USY-5.2)和 7.094-4.876 微摩尔/克(VUSY-12)减少到 9.826 微摩尔/克。XPS 证实了 Ni2+ 状态。使用正庚烷进行的催化裂化测试表明,随着镍浓度的增加,C5-C6 烷烃、烯烃、氢气和甲烷的产率也随之增加,Y-5.1 的产率分别为 64%、28%、79% 和 68%;USY-5.2 的产率分别为 62%、28%、76% 和 62%;VUSY-12 的产率分别为 58%、21%、75% 和 60%。观察到较重的成分相应减少。该研究表明,镍改性对沸石-Y 的理化性质和催化性能有显著影响,而这在很大程度上取决于 SiO2/Al2O3 的比例。该研究进一步揭示了沸石中掺杂镍所引起的结构和催化改性,突出了镍改性沸石在促进产生不良氢气和气体方面的潜力。
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引用次数: 0
Facile one-pot synthesis of photoresponsive Cu1.8S and CuInS2 nanostructures aided by Cu-pyrimidylthiolate molecular precursor 在嘧啶硫酸铜分子前驱体的帮助下,轻松实现光致伸缩性 Cu1.8S 和 CuInS2 纳米结构的一锅合成
Pub Date : 2024-10-30 DOI: 10.1016/j.nxmate.2024.100414
Suraj Peerappa Yadav , Adish Tyagi , Alpa Y. Shah , Deepak Tyagi , Sanjay Kumar , Gourab Karmakar , Rohit Singh Chauhan , Afsar Ali Siddiki
Copper-based binary and ternary sulfides have attracted significant attention due to their excellent photo-physical properties, making them highly promising for high-performance energy harvesting and storage devices. This study focuses on the synthesis and structural characterization of an air-stable hexanuclear Cu-pyrimidylthiolate cluster complex which serves as an efficient single-source precursor for the preparation of Cu1.8S nanocrystals. Furthermore, coupling the molecular precursor with suitable indium source resulted in a facile one-pot pathway for the preparation of technologically important, copper-based ternary CuInS₂, nanocrystals. The crystal structure, phase purity, and compositions of the nanostructures were confirmed using PXRD, XPS, EDS, and area elemental mapping. Electron microscopic studies revealed the formation of polygonal and hexagonal morphology with varied size in Cu1.8S and CuInS₂ nanocrystals respectively. UV-Vis diffuse reflectance spectroscopy showed a slight blue shift in the band gap of the nanostructures compared to their bulk counterparts which can be attributed to quantum confinement or surface lattice distortion effects. The band gap of the pristine nanocrystals along with high photocurrent and stable photo-switching characteristics suggest that they can serve as suitable electrode material for optoelectronic and photodetector devices.
铜基二元和三元硫化物因其优异的光物理性质而备受关注,这使得它们在高性能能量收集和存储设备中大有可为。本研究重点关注空气稳定的六核嘧啶硫代铜簇合物的合成和结构表征,该簇合物是制备 Cu1.8S 纳米晶体的高效单源前驱体。此外,将分子前驱体与合适的铟源耦合后,可通过简单的一锅法制备出具有重要技术意义的铜基三元 CuInS₂纳米晶体。利用 PXRD、XPS、EDS 和区域元素图谱确认了纳米结构的晶体结构、相纯度和成分。电子显微镜研究显示,Cu1.8S 和 CuInS₂纳米晶体分别形成了大小不一的多边形和六边形形态。紫外-可见漫反射光谱显示,与块状晶体相比,纳米结构的带隙发生了轻微的蓝移,这可能是量子约束或表面晶格畸变效应所致。原始纳米晶体的带隙以及高光电流和稳定的光开关特性表明,它们可以作为光电和光探测器件的合适电极材料。
{"title":"Facile one-pot synthesis of photoresponsive Cu1.8S and CuInS2 nanostructures aided by Cu-pyrimidylthiolate molecular precursor","authors":"Suraj Peerappa Yadav ,&nbsp;Adish Tyagi ,&nbsp;Alpa Y. Shah ,&nbsp;Deepak Tyagi ,&nbsp;Sanjay Kumar ,&nbsp;Gourab Karmakar ,&nbsp;Rohit Singh Chauhan ,&nbsp;Afsar Ali Siddiki","doi":"10.1016/j.nxmate.2024.100414","DOIUrl":"10.1016/j.nxmate.2024.100414","url":null,"abstract":"<div><div>Copper-based binary and ternary sulfides have attracted significant attention due to their excellent photo-physical properties, making them highly promising for high-performance energy harvesting and storage devices. This study focuses on the synthesis and structural characterization of an air-stable hexanuclear Cu-pyrimidylthiolate cluster complex which serves as an efficient single-source precursor for the preparation of Cu<sub>1.8</sub>S nanocrystals. Furthermore, coupling the molecular precursor with suitable indium source resulted in a facile one-pot pathway for the preparation of technologically important, copper-based ternary CuInS₂, nanocrystals. The crystal structure, phase purity, and compositions of the nanostructures were confirmed using PXRD, XPS, EDS, and area elemental mapping. Electron microscopic studies revealed the formation of polygonal and hexagonal morphology with varied size in Cu<sub>1.8</sub>S and CuInS₂ nanocrystals respectively. UV-Vis diffuse reflectance spectroscopy showed a slight blue shift in the band gap of the nanostructures compared to their bulk counterparts which can be attributed to quantum confinement or surface lattice distortion effects. The band gap of the pristine nanocrystals along with high photocurrent and stable photo-switching characteristics suggest that they can serve as suitable electrode material for optoelectronic and photodetector devices.</div></div>","PeriodicalId":100958,"journal":{"name":"Next Materials","volume":"7 ","pages":"Article 100414"},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142540051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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