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PANI/g-C3N4/CeO2 Nanocomposite for Photodegradation of Diazinon in Aqueous Solution PANI/g-C3N4/CeO2纳米复合材料在水溶液中光降解重氮肼
Pub Date : 2021-03-29 DOI: 10.2139/SSRN.3825594
A. Hussen
Diazinon is one of organophosphate pesticides which it is classified as a relatively dangerous substance (Class II by WHO). The PANI/g C3N4/ CeO2 nanocomposite was synthesized by in situ polymerization method to determine the efficiency of photocatalytic degradation of diazinon. The photocatalytic activities efficiencies of the supported and unsupported nanocomposites were evaluated using diazinon as a model pollutant. The superior photocatalytic effect of the PANI/g C3N4/CeO2 nanocomposite is attributed to the synergistic effect of PANI and g C3N4/CeO2 which promotes migration efficiency of the photogenerated carriers on the g C3N4/CeO2 nanocomposite interface. The effects of pH, initial diazinon concentration, catalyst load, hydrogen peroxide as well as effect of other organic compound were investigated using photocatalytic degradation of PANI/g C3N4/CeO2. The results obtained indicate the efficient degradation at pH= 6 which extent to 94.08 %, at 10 ppm extent to 88.9%, at 0.1 g/L extent to 97.48 %; were as increasing the concentration of hydrogen peroxide, the percent of degradation of diazinon increased due to the increased reaction between hydrogen peroxide and electron in the conduction band of PANI/g-C3N4/CeO2. Hydrogen peroxide can effectively inhibited electron hole recombination. Therefore hydrogen peroxide is better electron acceptor than dissolved oxygen; it acts as an alternative electron acceptor to oxygen. The effect of different organic compound on the photocatalytic degradation of diazinon; organic compound such as phenol, citric acid, EDTA and oxalic acid were examined, the result indicated that photocatalytic degradation was negatively affected in the presence of all organic compounds.
二嗪农是一种有机磷农药,被世界卫生组织列为相对危险物质(II类)。采用原位聚合法制备了PANI/g C3N4/ CeO2纳米复合材料,考察了其光催化降解重氮肼的效率。以二嗪农为模型污染物,评价了负载型和非负载型纳米复合材料的光催化活性和效率。PANI/g C3N4/CeO2纳米复合材料之所以具有优异的光催化效果,是因为PANI与g C3N4/CeO2的协同作用提高了光生载体在g C3N4/CeO2纳米复合材料界面上的迁移效率。通过光催化降解PANI/g C3N4/CeO2,考察了pH、初始二氮肼浓度、催化剂负荷、过氧化氢以及其他有机化合物的影响。结果表明:pH= 6时的有效降解率为94.08%,10 ppm时的有效降解率为88.9%,0.1 g/L时的有效降解率为97.48%;随着过氧化氢浓度的增加,由于过氧化氢与PANI/g-C3N4/CeO2导电带中电子的反应增加,二嗪酮的降解率增加。过氧化氢能有效抑制电子空穴复合。因此,过氧化氢是比溶解氧更好的电子受体;它充当氧的替代电子受体。不同有机化合物对光催化降解二嗪农的影响对苯酚、柠檬酸、EDTA和草酸等有机化合物进行了检测,结果表明,所有有机化合物的存在都对光催化降解产生负面影响。
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引用次数: 4
Using Grain Boundary Irregularity to Quantify Dynamic Recrystallization in Ice 用晶界不规则性量化冰的动态再结晶
Pub Date : 2021-03-15 DOI: 10.2139/ssrn.3762203
Sheng Fan, D. Prior, A. Cross, D. Goldsby, T. Hager, M. Negrini, Chao Qi
Abstract Dynamic recrystallization is an important mechanical weakening mechanism during the deformation of ice, yet we currently lack robust quantitative tools for identifying recrystallized grains in the “migration” recrystallization regime that dominates ice deformation at temperatures close to the ice melting point. Here, we propose grain boundary irregularity as a quantitative means for discriminating between recrystallized (high sphericity, low irregularity) and remnant (low sphericity, high irregularity) grains. To this end, we analyzed cryogenic electron backscatter diffraction (cryo-EBSD) data of deformed polycrystalline ice, to quantify dynamic recrystallization using grain boundary irregularity statistics. Grain boundary irregularity has an inverse relationship with a sphericity parameter, Ψ , defined as the ratio of grain area and grain perimeter, divided by grain radius in 2-D so that the measurement is grain size independent. Sphericity ( Ψ ) typically decreases with increasing grain size, up to a threshold grain size, above which Ψ either plateaus (at temperature, T -10°C) or increases much more gradually (at T ≥ -10°C). There is no apparent relationship between grain sphericity and grain c-axis orientation even at very high temperatures (-4 and -5°C), where GBM dominants, suggesting little crystallographic control on the activity of grain boundary migration (GBM). Decreasing sphericity up to the threshold grain size can be explained by newly-formed, small, spherical recrystallized grains growing via strain-induced GBM and thereby developing increasingly irregular grain boundaries. We suggest that the plateau (or gradual decrease) in sphericity at larger sizes represents a population of original grains (i.e., remnant grains) that becomes increasingly irregular (at similar rates) due to the balance between GBM and nucleation. In this interpretation, the threshold grain size represents the largest grain size reached by a growing recrystallized grain by the end of an experiment. Thus, grain boundary irregularity provides a means for discriminating between recrystallized and remnant grains—a capability that is potentially useful for evaluating dynamic recrystallization processes in ice deformed at temperatures close to the melting point. The threshold grain size and experiment duration can be used to calculate the rates of recrystallization and grain size evolution associated with GBM. Grain size evolution rates are similar at high and low temperatures, suggesting similar GBM rates. Previous studies show that grain boundary mobility decreases with decreasing temperature. The driving force of GBM, on the other hand, has a positive correlation with stress, which increases with a decreasing temperature if strain rate remains unchanged. The balance between boundary mobility and driving force is likely the cause of similar GBM rates between high and low temperatures.
动态再结晶是冰变形过程中的一种重要的力学弱化机制,但目前我们缺乏可靠的定量工具来识别在接近冰熔点的温度下主导冰变形的“迁移”再结晶机制中的再结晶晶粒。在这里,我们提出晶界不规则性作为区分再结晶(高球度,低不规则性)和残余(低球度,高不规则性)晶粒的定量手段。为此,我们分析了变形多晶冰的低温电子背散射衍射(cryo-EBSD)数据,利用晶界不规则性统计来量化动态再结晶。晶界不规则性与球度参数Ψ呈反比关系,球度参数定义为晶粒面积与晶粒周长之比除以二维晶粒半径,因此测量与晶粒尺寸无关。球形度(Ψ)通常随着晶粒尺寸的增加而降低,直至一个阈值晶粒尺寸,高于该阈值Ψ或趋于稳定(温度为-10°C),或逐渐增加(温度≥-10°C)。即使在极高温(-4℃和-5℃)下,晶粒球度和晶粒C轴取向之间也没有明显的关系,其中晶界迁移占主导地位,这表明晶界迁移(GBM)的活性几乎没有晶体学控制。球度下降到阈值晶粒尺寸可以解释为通过应变诱导的GBM生长新形成的小球形再结晶晶粒,从而形成越来越不规则的晶界。我们认为,在较大尺寸下,球形度的平台(或逐渐减少)代表原始晶粒(即残余晶粒)的种群,由于GBM和形核之间的平衡,它们变得越来越不规则(以相似的速率)。在这种解释中,阈值晶粒尺寸表示在实验结束时生长的再结晶晶粒所达到的最大晶粒尺寸。因此,晶界不规则性提供了一种区分再结晶和残余晶粒的方法,这种能力对于评估在接近熔点的温度下变形的冰的动态再结晶过程是潜在有用的。阈值晶粒尺寸和实验时间可以用来计算与GBM相关的再结晶速率和晶粒尺寸演变。在高温和低温条件下,晶粒尺寸演化速率相似,表明GBM速率相似。以往的研究表明,晶界迁移率随温度的降低而降低。另一方面,GBM的驱动力与应力呈正相关,在应变速率不变的情况下,随着温度的降低,驱动力增大。边界迁移率和驱动力之间的平衡可能是高温和低温之间类似的GBM速率的原因。
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引用次数: 14
Exploring Electroactive Microenvironments in Polymer-Based Nanocomposites to Sensitize Bacterial Cells to Low Doses of Antimicrobials 探索聚合物基纳米复合材料中的电活性微环境以使细菌细胞对低剂量抗菌素敏感
Pub Date : 2021-03-15 DOI: 10.2139/ssrn.3805156
J. Moreira, M. Fernandes, Estela O. Carvalho, A. Nicolau, V. Lazić, V. Lazić, J. Nedeljković, S. Lanceros‐Méndez
The search for novel antimicrobial strategies capable of avoiding resistance mechanisms in bacteria are highly needed due to the alarming emergence of antimicrobial resistance. The application of physical stimuli as a mean of sensitizing bacteria for the action of antimicrobials on otherwise resistant bacteria or by allowing the action of an extremely low quantity of antimicrobials may be seen as a breakthrough for such purpose. This work proposes the development of antibacterial nanocomposites using the synergy between the electrically active microenvironments, created by a piezoelectric polymer (poly(vinylidene fluoride-co-trifluoroethylene) (PVDF-TrFE)), with green-synthesized silver nanoparticles (AgNPs). The electrical microenvironment is generated via mechanical stimulation of piezoelectric PVDF-TrFE/AgNPs films using a lab-made mechanical bioreactor. The generated material’s electrical response further translates to bacterial cells, which in combination with AgNPs and the specific morphological features of the material induce important antibacterial and antibiofilm activity. Both porous and non-porous PVDF composites have shown antibacterial characteristics when stimulated at a mechanical frequency of 4Hz being the effect boosted when AgNPs were incorporated in the nanocomposite, reducing in more than 80 % the bacterial growth in planktonic and biofilm form. The electroactive environments sensitize the bacteria allowing the action of extremely low doses of AgNPs. Importantly, the material did not compromise the viability of mammalian cells, thus being considered biocompatible. The piezoelectric stimulation of PVDF-based polymeric films may represent a breakthrough in the development of antibacterial coatings for devices used at hospital setting, taking advantage on the use of mechanical stimuli (pressure/touch) to exert antibacterial and antibiofilm activity.
由于抗生素耐药性的惊人出现,迫切需要寻找能够避免细菌耐药机制的新型抗菌策略。应用物理刺激作为致敏细菌的手段,使抗菌素对其他耐药细菌起作用,或通过允许极少量的抗菌素起作用,可被视为实现这一目的的突破。这项工作提出了利用压电聚合物(聚偏氟乙烯-共三氟乙烯)(PVDF-TrFE)产生的电活性微环境与绿色合成的银纳米颗粒(AgNPs)之间的协同作用来开发抗菌纳米复合材料。电微环境是通过使用实验室制造的机械生物反应器对压电PVDF-TrFE/AgNPs薄膜进行机械刺激而产生的。生成的材料的电响应进一步转化为细菌细胞,细菌细胞与AgNPs和材料的特定形态特征结合,诱导出重要的抗菌和抗生物膜活性。当机械频率为4Hz时,多孔和非多孔PVDF复合材料都显示出抗菌特性,当纳米复合材料中加入AgNPs时,效果得到增强,浮游和生物膜形式的细菌生长减少了80%以上。电活性环境使细菌敏感,允许极低剂量的AgNPs的作用。重要的是,这种材料不会损害哺乳动物细胞的生存能力,因此被认为是生物相容性的。利用机械刺激(压力/触摸)来发挥抗菌和抗生物膜活性,pvdf基聚合物薄膜的压电刺激可能代表了医院设备抗菌涂层发展的一个突破。
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引用次数: 0
Experimentally Validated Constitutive Model for NiTi-based Shape Memory Alloys Featuring Intermediate R-phase Transformation: A Case Study of Ni 48 Ti 49 Fe 3 niti基形状记忆合金中间r相变本构模型的实验验证——以ni48ti 49fe3为例
Pub Date : 2021-03-15 DOI: 10.2139/ssrn.3805227
Mark. Frost, Alan Jurysta, L. Heller, P. Sedlák
An important group of NiTi-based alloys employed in applications exhibits an intermediate R-phase transformation, which substantially modifies the material’s thermomechanical response. Finite element analysis of products from such alloys requires a constitutive model covering the two-stage transformation sequence in its full thermodynamic nature. We propose an enhanced constitutive model for NiTi-based alloys, which incorporates R-phase as a distinctive phase with loading-dependent transformation strain. We validate the model on a newly acquired extensive experimental dataset on the thermomechanical response of Ni48 Ti49 Fe3 shape memory alloy and illustrate the capabilities of its implementation into finite element software on a computational structural analysis of a tightening ring.
应用中使用的一组重要的镍钛基合金表现出中间的r相变,这大大改变了材料的热机械响应。这种合金产品的有限元分析需要一个涵盖两阶段转化序列的本构模型,其全部热力学性质。我们提出了一种增强的niti基合金本构模型,该模型将r相作为一个具有载荷依赖转变应变的独特相。我们在新获得的Ni48 Ti49 Fe3形状记忆合金的热力学响应实验数据集上验证了该模型,并说明了将其应用于有限元软件的能力,用于拧紧环的计算结构分析。
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引用次数: 1
Effect of Twin Schmid Factor on the Tension Twinning Activities in a Highly Textured Mg-3Al-1Zn 孪晶施密德因子对高织构Mg-3Al-1Zn拉伸孪晶活性的影响
Pub Date : 2021-03-15 DOI: 10.2139/ssrn.3805155
Dexin Zhao, Jiaqi Dong, K. Xie
We investigated the effect of twin Schmid factor on the tension twinning of individual grains in deformed textured Mg-3Al-1Zn samples. The samples were deformed to ~3% strain (normal-direction compression and tension, rolling-direction compression and tension, and 45 o compression). Statistical analyses on the electron backscatter diffraction results revealed tension twinning generally obeys the Schmid law for individual grains, regardless of whether the global stress state favors tension twinning or not. The strong dependence of tension twinning on Schmid factor is in contrast to the reported weak correlation of dislocations and Schmid factor in the same material system. Such observations are anticipated to advance the understanding of the Schmid factor effect on the deformation behavior of polycrystalline Mg alloys.
研究了孪晶施密德因子对变形织构Mg-3Al-1Zn试样中单个晶粒拉伸孪晶的影响。试样变形至~3%应变(法向压缩和拉伸,滚动方向压缩和拉伸,45度压缩)。对电子背散射衍射结果的统计分析表明,无论整体应力状态是否有利于张力孪晶,单个晶粒的张力孪晶总体上遵循施密德定律。张力孪晶对施密德因子的依赖性很强,而在同一材料体系中,位错与施密德因子的相关性较弱。这些观察结果有望促进对施密德因子对多晶镁合金变形行为影响的理解。
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引用次数: 0
Towards the Translation of Electroconductive Organic Materials for Regeneration of Neural Tissues 导电性有机材料在神经组织再生中的应用
Pub Date : 2021-03-11 DOI: 10.2139/ssrn.3802820
Eleana Manousiouthakis, Junggeon Park, John G Hardy, Jae Young Lee, Christine E Schmidt
Carbon-based conductive and electroactive materials (e.g., derivatives of graphene, fullerenes, polypyrrole, polythiophene, polyaniline) have been studied since the 1970s for use in a broad range of applications. These materials have electrical properties comparable to those of commonly used metals, while providing other benefits such as flexibility in processing and modification with biologics (e.g., cells, biomolecules), to yield electroactive materials with biomimetic mechanical and chemical properties. In this review, we focus on the uses of these electroconductive materials in the context of the central and peripheral nervous system, specifically recent studies in the peripheral nerve, spinal cord, brain, eye, and ear. We also highlight in vivo studies and clinical trials, as well as a snapshot of emerging classes of electroconductive materials (e.g., biodegradable materials). We believe such specialized electrically conductive biomaterials will clinically impact the field of tissue regeneration in the foreseeable future. STATEMENT OF SIGNIFICANCE: This review addresses the use of conductive and electroactive materials for neural tissue regeneration, which is of significant interest to a broad readership, and of particular relevance to the growing community of scientists, engineers and clinicians in academia and industry who develop novel medical devices for tissue engineering and regenerative medicine. The review covers the materials that may be employed (primarily focusing on derivatives of fullerenes, graphene and conjugated polymers) and techniques used to analyze materials composed thereof, followed by sections on the application of these materials to nervous tissues (i.e., peripheral nerve, spinal cord, brain, optical, and auditory tissues) throughout the body.
自20世纪70年代以来,碳基导电和电活性材料(例如石墨烯、富勒烯、聚吡咯、聚噻吩、聚苯胺的衍生物)已被研究用于广泛的应用。这些材料具有与常用金属相当的电学性能,同时提供其他优点,例如与生物制剂(例如细胞,生物分子)加工和改性的灵活性,以产生具有仿生机械和化学性能的电活性材料。在这篇综述中,我们重点介绍了这些导电材料在中枢和周围神经系统中的应用,特别是最近在周围神经、脊髓、脑、眼和耳方面的研究。我们还重点介绍了体内研究和临床试验,以及新兴导电材料(例如,可生物降解材料)的概况。我们相信,在可预见的未来,这种专门的导电生物材料将在临床上影响组织再生领域。意义声明:这篇综述论述了导电和电活性材料在神经组织再生中的应用,这是广大读者感兴趣的,特别是与学术界和工业界不断增长的科学家、工程师和临床医生群体有关,他们为组织工程和再生医学开发了新型医疗设备。该综述涵盖了可能使用的材料(主要集中在富勒烯、石墨烯和共轭聚合物的衍生物)和用于分析其组成材料的技术,然后是将这些材料应用于全身神经组织(即周围神经、脊髓、大脑、光学和听觉组织)的部分。
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引用次数: 26
Simultaneously Improved Strength and Impact Toughness by Introducing Ultrafine Ferrite in Low-Temperature Bainitic Steel 在低温贝氏体钢中引入超细铁素体,同时提高了强度和冲击韧性
Pub Date : 2021-03-04 DOI: 10.2139/ssrn.3797416
T. Zhao, X. Jia, Chen Chen, Fucheng Zhang, Tiansheng Wang
Ultrafine ferrite with a grain size range of 0.5-2 μm was introduced into low-temperature bainitic medium-carbon high-silicon steel through partially austenitization of cold-rolled tempered troostite followed by austempering at temperatures of 10 °C above martensite starting temperature. The microstructures and mechanical properties were studied and compared with conventional low-temperature bainitic steel obtained by full austenitization of cold-rolled tempered troostite followed by austempering at a temperature of 10 °C above martensite starting temperature. The results show that introduction of ~4 vol% ultrafine ferrite into low-temperature bainite can simultaneously enhance the ultimate tensile strength, yield strength, and impact toughness to 1614 MPa, 1074 MPa, and 52 J (half-width Charpy U-notch specimen) without loss of ductility, increasing by approximately 6.5%, 12.5%, and 62.5%, respectively.
在高于马氏体起始温度10℃的温度下,通过冷轧回火蠕变体的部分奥氏体化,向低温贝氏体中碳高硅钢中引入了晶粒尺寸为0.5 ~ 2 μm的超细铁素体。研究了该钢的显微组织和力学性能,并与在高于马氏体起始温度10℃的条件下,经冷轧回火直纹体完全奥氏体化后再等温回火得到的普通低温贝氏体钢进行了比较。结果表明:在低温贝氏体中加入~4 vol%的超细铁素体,在不损失延性的情况下,可将贝氏体的极限抗拉强度、屈服强度和冲击韧性分别提高至1614 MPa、1074 MPa和52 J(半宽Charpy u型缺口试样),分别提高约6.5%、12.5%和62.5%。
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引用次数: 2
Challenges to Accurate Evaluation of Bulk Hardness from Nanoindentation Testing at Low Indent Depths 低压痕深度纳米压痕测试中准确评估体硬度的挑战
Pub Date : 2021-03-01 DOI: 10.2139/ssrn.3793936
Pengcheng Zhu, Yajie Zhao, Shradha Agarwal, J. Hay, J. Henry, S. Zinkle
Estimations of bulk hardness from nanoindentation data are frequently subject to considerable uncertainties, due to indentation size effects, potential pileup effects, and potential influence of surface quality or test methods. In this study, we examined materials science principles of nanoindentation test methods to enable accurate prediction of bulk hardness for a series of high purity Fe and Fe alloys containing 3-25 wt. %Cr. These materials were tested in as-annealed and thermally aged (100-900 hours at 475 oC for 14-25 wt. %Cr) conditions to produce Cr-rich a’ precipitates of varying size and density (bulk Vickers hardness values of ~50 to 350 VHN). Nanoindentation performed with a Berkovich indenter using constant strain rate (0.05 to 0.5 /s) and constant loading rate test methods provided comparable bulk equivalent hardness (H0) extracted by Nix-Gao model, indicating a weak strain rate sensitivity of the investigated materials at room temperature. Results from electropolished and fine mechanically polished samples were found to give comparable measured hardness. Conversely, material pileup adjacent to the indented area produced a 7-20% correction to the indent contact area. The Nix-Gao fitted nanoindentation H0 after pileup corrections agreed quantitatively better with the bulk Vickers hardness than the uncorrected H0 values. The model-predicted (dispersed barrier hardening superposition) and measured strength values agreed for aged Fe18Cr, indicating that Nix-Gao model combined with pileup corrections significantly improved the accuracy of hardness evaluation by nanoindentation. Analytic and experimental analyses demonstrate that inappropriate methods such as hardness ratios or changes at a reference depth (applied in many prior nanoindentation studies) can cause quantitative errors in bulk hardness estimates as large as 60% due to indentation size effects.
由于压痕尺寸效应、潜在的堆积效应以及表面质量或测试方法的潜在影响,从纳米压痕数据中估计体硬度经常受到相当大的不确定性。在这项研究中,我们研究了纳米压痕测试方法的材料科学原理,以便准确预测一系列含3- 25wt . %Cr的高纯铁和铁合金的体硬度。这些材料在退火和热时效(在475℃,14- 25wt . %Cr, 100-900小时)条件下进行测试,产生不同尺寸和密度的富Cr a '沉淀(体维氏硬度值约50至350 VHN)。采用恒应变速率(0.05 ~ 0.5 /s)和恒加载速率测试方法使用Berkovich压头进行纳米压痕测试,获得的体等效硬度(H0)与采用Nix-Gao模型提取的硬度相当,表明所研究材料在室温下应变速率敏感性较弱。结果发现,电抛光和精细机械抛光样品的测量硬度相当。相反,靠近压痕区域的材料堆积会对压痕接触区域产生7-20%的修正。与未校正的H0值相比,经过堆积校正后的Nix-Gao拟合的纳米压痕H0值与体维氏硬度的定量一致性更好。时效Fe18Cr的模型预测值(分散障碍硬化叠加)与实测值一致,表明结合堆积修正的Nix-Gao模型显著提高了纳米压痕硬度评估的准确性。分析和实验分析表明,不适当的方法,如硬度比或参考深度的变化(在许多先前的纳米压痕研究中应用)可能导致由于压痕尺寸影响而导致体硬度估计的定量误差高达60%。
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引用次数: 1
Downshifting and Antireflective Thin Films for Solar Module Power Enhancement 用于太阳能组件功率增强的降档和抗反射薄膜
Pub Date : 2021-03-01 DOI: 10.2139/ssrn.3805247
Yujuan He, Jie Liu, S. Sung, Chih-hung Chang
Abstract Efforts to enhance the solar conversion efficiency have prevailed for decades. There is a growing interest in improving the spectral response of solar modules, especially in harvesting UV photons, which offer intense energy in a narrow wavelength range. To harvest UV photons and reduce reflection without interfering with the formulas and manufacturing process of solar cells, in this work, thin films that possess downshifting and antireflection capabilities were fabricated on the cover glass of multicrystalline Si solar cells. The thin films were composed of graded index layers of europium-doped yttrium orthovanadate (YVO4:Eu) and hollow silica nanoparticles (HSNPs). The design of the composite thin films was assisted by the FDTD mathematical model that simulated the refractive index and thickness of each layer to obtain the optimum transmittance. The cover glass with multifunctional thin films harvested more than 30% of UV photons and enhanced the solar conversion efficiency by 4.12% at normal incidence compared to the uncoated cover glass.
提高太阳能转换效率的努力已经盛行了几十年。人们对提高太阳能组件的光谱响应越来越感兴趣,特别是在收集紫外光子方面,它在狭窄的波长范围内提供强烈的能量。为了在不影响太阳能电池的配方和制造工艺的情况下收集紫外线光子并降低反射,本研究在多晶硅太阳能电池的盖板玻璃上制备了具有降移和抗反射能力的薄膜。该薄膜由掺杂铕的正钒酸钇(YVO4:Eu)和空心二氧化硅纳米颗粒(HSNPs)组成。利用时域有限差分(FDTD)数学模型模拟各层薄膜的折射率和厚度,以获得最佳透光率。与未涂覆的盖板玻璃相比,具有多功能薄膜的盖板玻璃捕获了超过30%的紫外光子,在正入射下太阳能转换效率提高了4.12%。
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引用次数: 10
Self-Organized High-Hardness Thermal Spray Coatings 自组织高硬度热喷涂涂层
Pub Date : 2021-02-26 DOI: 10.2139/ssrn.3793930
I. McCue, B. Gaskey, Michael C. Brupbacher, W. M. Buchta, A. Chuang, K. Xie, W. Kuo, J. Erlebacher
We present a new dealloying-based technique to form fully-dense and high-hardness metal composite coatings. By depositing then heat treating a TiCr alloy coating on a Ni-base superalloy, a eutectic reaction occurs at the coating/substrate interface, which drives spontaneous pattern formation in both alloys analogous to liquid metal dealloying. The coating exhibits a significantly higher hardness (15 GPa) than both the starting alloy (3.7 GPa) and precursor coating (6 GPa), measured by micro- and nanoindentation, while maintaining the ability to plastically deform during micro-indentation experiments without apparent cracking or spallation. The flexibility and scalability of the dealloying process used here demonstrates a promising route towards protective coatings for structural alloys.
提出了一种以脱合金为基础的制备全致密高硬度金属复合镀层的新方法。通过在镍基高温合金上沉积并热处理TiCr合金涂层,在涂层/基体界面处发生共晶反应,从而在两种合金中自发形成类似于液态金属合金化的图案。通过微压痕和纳米压痕测量,涂层的硬度(15 GPa)明显高于起始合金(3.7 GPa)和前驱体涂层(6 GPa),同时在微压痕实验中保持塑性变形的能力,没有明显的开裂或剥落。本文所采用的脱合金工艺的灵活性和可扩展性为结构合金的保护涂层提供了一条有前途的途径。
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引用次数: 1
期刊
Materials Science eJournal
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