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Synthesis of multifunctional azo dyes based organic electroactive material: Efficient redox couple for aqueous redox flow batteries 基于偶氮染料的多功能有机电活性材料的合成:水氧化还原液流电池的高效氧化还原偶联
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-22 DOI: 10.1016/j.mtsust.2025.101294
Shakira Allahbaksh , Ata-ur- Rehman , Safyan Akram Khan , Shahid Ali , Muhammad Nawaz Tahir , Muhammad Mansha , Majad Khan
The synthesis, electrochemical properties, and application of a novel multifunctional azo dye (MFAD), containing sulfonated and carboxylated naphthalene groups, were explored for aqueous organic redox flow batteries (AORFBs). MFAD was synthesized via a diazo coupling of 3-aminobenzoic acid with 5-amino-2-naphthalenesulfonic acid, resulting in a 97 % yield. Electrochemical testing was carried out using potassium ferrocyanide and potassium permanganate as catholytes with the MFAD as anolyte in different conditions, i.e., MFAD was dissolved in 1M KOH and made two different supporting electrolyte systems: (i) urea with KCl (MFAD1) and (ii) urea, KCl, and Na3PO4 (MFAD2). At a lower current (0.01 A), MFAD1 showed stable charging for 143 cycles but suffered discharge instability after 15 cycles, reducing coulombic efficiency from 99 % to 50 %. Higher current (0.03 A) with supporting electrolytes significantly improved charge capacity and stability. MFAD1 demonstrated a higher average volumetric charge capacity (1200.2 mAh L−1) and average discharge capacity (829.3 mAh L−1), whereas MFAD2, although showing a slightly lower discharge capacity (818.6 mAh L−1), delivered superior coulombic efficiency (76.5 %) compared to MFAD1 (68.8 %). To further assess MFAD's full cell performance, MFAD was further paired with KMnO4 (0.2 M in 1M KOH) without any supporting electrolyte. Under a current of 0.03 A and 10 min cycling, the MFAD/KMnO4 cell achieved an average discharge capacity of 128.4 mAh L−1, maintaining 80 % capacity retention and a coulombic efficiency of 77 %. Long-term cycling over 47.3 h demonstrated excellent stability and had also retained 97 % of the initial capacity. Compared to MFAD1 and MFAD2, the MFAD/KMnO4 system outperformed in stability and coulombic efficiency, highlighting MFAD's strong potential as a scalable and efficient anolyte for high-performance AORFBs. Overall, these findings emphasize the promising role of azobenzene-based molecules for advancing next-generation energy storage systems.
研究了一种新型萘磺酸基和羧化萘基多功能偶氮染料(MFAD)的合成、电化学性能及其在有机氧化还原液流电池(AORFBs)中的应用。采用3-氨基苯甲酸与5-氨基-2-萘磺酸重氮偶联法制备了MFAD,收率为97% %。以亚铁氰化钾和高锰酸钾为阴极电解质,MFAD为阳极电解质,在不同条件下进行电化学测试,即MFAD溶解在1M KOH中,制成两种不同的支撑电解质体系:(i)尿素- KCl (MFAD1)和(ii)尿素- KCl - Na3PO4 (MFAD2)。在较低电流(0.01 a)下,MFAD1在143次循环中稳定充电,但在15次循环后放电不稳定,库仑效率从99 %降低到50 %。更高的电流(0.03 A)与配套电解质显著提高充电容量和稳定性。MFAD1具有较高的平均体积充电容量(1200.2 mAh L−1)和平均放电容量(829.3 mAh L−1),而MFAD2的放电容量(818.6 mAh L−1)略低于MFAD1,但库仑效率(76.5 %)优于MFAD1(68.8 %)。为了进一步评估MFAD的全电池性能,MFAD进一步与KMnO4(0.2 M in 1M KOH)配对,没有任何支持电解质。在0.03 a电流和10 min循环下,MFAD/KMnO4电池的平均放电容量为128.4 mAh L−1,容量保持率为80% %,库仑效率为77 %。在47.3 h以上的长期循环表现出优异的稳定性,并且还保留了97% %的初始容量。与MFAD1和MFAD2相比,MFAD/KMnO4体系在稳定性和库仑效率方面表现优于MFAD1和MFAD2,凸显了MFAD作为高性能主动脉主动脉fb的可扩展高效阳极电解质的强大潜力。总的来说,这些发现强调了偶氮苯基分子在推进下一代储能系统方面的有希望的作用。
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引用次数: 0
Clay nanostructures in geotechnical engineering: A critical review of mechanisms, performance, and sustainable soil stabilization 粘土纳米结构在岩土工程:机制,性能和可持续土壤稳定的关键审查
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-22 DOI: 10.1016/j.mtsust.2025.101284
Amira S. Diab , Ahmed A. Allam , Hassan A. Rudayni , Khaled M. Abdelfadil , Hasan Arman , Wail Al Zoubi , Mostafa R. Abukhadra
The growing demand for resilient and low-carbon geotechnical infrastructure has intensified interest in clay-based nanostructures as next-generation soil stabilizers. Although many studies have examined individual nanoclays or specific stabilization outcomes, a unified multi-scale synthesis linking nanostructure geometry (0D, 1D, 2D), micro-mechanisms, and engineering performance remains largely absent. This review addresses this gap by evaluating allophane-type 0D nanoparticles, halloysite nanotubes and fibrous silicates (1D), and layered nanosheets of kaolinite, illite, and smectite (2D), emphasizing how their morphologies govern pozzolanic activity, electrostatic flocculation, double-layer modification, and microstructural densification. Microstructural evidence (SEM/TEM, XRD, MIP) shows that 0D nanoclays accelerate nucleation, 1D nanotubes enhance crack-bridging and fabric interlocking, and 2D nanosheets yield the strongest improvements in stiffness, compressibility, and hydraulic resistance. Hybrid nanoclay–SCM–polymer systems exhibit strong synergistic effects, enabling superior performance at low dosages (0.1–2 %) and reducing cement demand and carbon emissions, though nanoclay-specific LCAs and long-term field validations remain limited. Despite promising results, challenges persist regarding dispersion quality, natural compositional variability, and the lack of standardized mix-design or quantitative dispersion metrics. Advancing this field requires improved dispersion strategies, multi-scale mechanistic modeling, environmental durability assessments, and comprehensive LCAs to translate laboratory findings into reliable field solutions. Overall, 0D–2D clay nanostructures offer a robust and sustainable platform for next-generation soil stabilization, bridging nano-engineering mechanisms with durable, low-carbon geotechnical practices.
对弹性和低碳岩土工程基础设施的需求不断增长,增强了人们对粘土基纳米结构作为下一代土壤稳定剂的兴趣。尽管许多研究已经研究了单个纳米粘土或特定的稳定结果,但在很大程度上仍然缺乏将纳米结构几何(0D, 1D, 2D),微观机制和工程性能联系起来的统一的多尺度合成。这篇综述通过评价allophane型0D纳米粒子、高岭土纳米管和纤维硅酸盐(1D)以及高岭石、伊利石和蒙脱石的层状纳米片(2D)来弥补这一空白,强调它们的形态如何影响火山灰活性、静电絮凝、双层改性和微观结构致密化。微观结构证据(SEM/TEM, XRD, MIP)表明,0D纳米粘土加速成核,1D纳米管增强裂缝桥接和织物互锁,而2D纳米片在刚度、可压缩性和水力阻力方面的改善最为明显。纳米粘土- scm -聚合物混合体系表现出强大的协同效应,在低剂量(0.1 - %)下实现卓越的性能,并减少水泥需求和碳排放,尽管纳米粘土特异性lca和长期现场验证仍然有限。尽管取得了令人鼓舞的成果,但分散质量、自然成分可变性、缺乏标准化混合设计或定量分散指标等方面的挑战依然存在。推进这一领域需要改进分散策略、多尺度机制建模、环境耐久性评估和综合lca,以将实验室发现转化为可靠的现场解决方案。总的来说,0D-2D粘土纳米结构为下一代土壤稳定提供了一个强大且可持续的平台,将纳米工程机制与耐用、低碳的岩土工程实践联系起来。
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引用次数: 0
Metal-oxide nanolaminate barrier coatings to enable large-scale manufacturing of sustainable flex packaging 金属氧化物纳米层压屏障涂层,使大规模生产的可持续柔性包装
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-22 DOI: 10.1016/j.mtsust.2025.101289
Denys Vidish , Soumyadeep Saha , Louis-Vincent Delumeau , Tristan Grovu , Kevin P. Musselman
The world is drowning in single-use-plastic waste. Compostable and recyclable alternatives to single-use flexible packaging exist but do not provide an adequate barrier to water-vapor and oxygen. We address this by using atmospheric-pressure spatial atomic layer deposition to apply Al2O3-ZnO nanolaminates on compostable polylactic acid (PLA) and recyclable polyethylene terephthalate (PET) films for flexible packaging. This industrially scalable coating is performed at 50 °C, preserving film integrity while enabling nanoscale control. The nanolaminate structure is found to enhance the bending resistance, improve the coating stability, and drastically reduce the water-vapor transmission rate (WVTR) and oxygen transmission rate (OTR). An optimized 8-stack Al2O3-ZnO nanolaminate that is ∼96 nm thick reduces the WVTR of PLA packaging film from ∼300 g m−2·24hr−1 to <0.5 g m−2·24hr−1 and its OTR from ∼1000 cm3 m−2·24hr−1 to <10 cm3 m−2·24hr−1 (both measured at 38oC and 90 % relative humidity), making it ideal for packaging air-sensitive goods. When the 8-stack nanolaminate is laminated between two PET films to form a simple packaging structure and is subjected to the harshest industry-standard Gelbo flex durability testing, it retains a WVTR <2 g m−2·24hr−1. These ultrathin coatings are well-positioned to meet recyclability and compostability standards, enabling a viable path to sustainable flex packaging.
世界正在被一次性塑料垃圾淹没。存在可堆肥和可回收的一次性软包装替代品,但不能提供足够的水蒸气和氧气屏障。我们利用常压空间原子层沉积技术将Al2O3-ZnO纳米层材料应用于可堆肥聚乳酸(PLA)和可回收聚对苯二甲酸乙二醇酯(PET)薄膜上,用于软包装。这种工业上可扩展的涂层在50 °C下进行,在保持薄膜完整性的同时实现纳米级控制。纳米层合结构增强了涂层的抗弯性能,提高了涂层的稳定性,并显著降低了水蒸气透过率(WVTR)和氧气透过率(OTR)。一个优化8-stack Al2O3-ZnO nanolaminate∼96 nm厚减少解放军包装膜的WVTR∼300 g −2·24 hr−1 & lt; 0.5 g m−2·24 hr−1及其工程从1000年∼ 立方厘米 m−2·24小时−1 & lt; 10 立方厘米 m−2·24小时−1(以38摄氏度和90年 %相对湿度),使其适合包装气敏商品。当8层纳米层压在两个PET薄膜之间形成简单的包装结构,并进行最严格的行业标准Gelbo弯曲耐久性测试时,它保持WVTR <;2 g m−2·24小时−1。这些超薄涂层很好地满足可回收性和可堆肥性标准,使可持续软包装成为可行的途径。
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引用次数: 0
Enhancing the phase, thermal stability, band gap energy, and surface area of iron oxide nanoparticles by varying reducing agents and examining their efficacy in photocatalytic dye degradation 通过改变还原剂并检查其光催化降解染料的功效,增强氧化铁纳米颗粒的相、热稳定性、带隙能和表面积
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-21 DOI: 10.1016/j.mtsust.2025.101285
Gemechu Fikadu Aaga , Workineh Mengesha Fereja , Tsion Guta Bekele
Iron oxide nanoparticles were synthesized using NaOH, NaBH4, and Calpurnia aurea leaf extract as reducing agents. XRD analysis confirmed the formation of hematite nanoparticles with rhombohedral structure when using NaOH and NaBH4 as reducing agents, having the average crystallite size of 28.2287 and 21.86575 nm, respectively. The iron oxide nanoparticles synthesized using Calpurnia aurea leaf extract were maghemite with a cubic spinal structure having an average crystallite size of 21.69002, 21.09579, and 19.61541 nm with leaf extract to precursor ratios of 1:2, 1:1, and 2:1, respectively. The FT-IR analysis demonstrated the formation of Fe-O bonds between 460 and 550 cm−1 and around 570 cm−1 for hematite and maghemite nanoparticles, respectively. The optical band gap energy calculation from DRS analysis gave the indirect band gap energy of 1.32 and 1.14 eV and direct band gap energy of 1.62 and 1.55 eV for hematite nanoparticles synthesized using NaOH and NaBH4, respectively. For maghemite nanoparticles synthesized with the leaf extract, indirect band gap energies of 1.62, 1.57, and 1.66 eV and direct band gap energies of 2.09, 2.09, and 2.20 eV were calculated for leaf extract to precursor ratios of 1:2, 1:1, and 2:1, respectively. The TGA-DTA analysis confirmed the improved thermal stability of the maghemite nanoparticles synthesized using the leaf extract. The hematite nanoparticles synthesized with NaOH exhibited a total weight loss of 27.278 % with three different endothermic peaks at 89.95, 31.79, and 650.79 °C, while a weak endothermic peak was observed for hematite nanoparticles obtained using NaBH4 at 94.25 °C. For the maghemite nanoparticles synthesized using leaf extract, the maximum weight loss observed is 8.192 % at a ratio of 1:1, while there are no endothermic or exothermic peaks observed for the three ratios. From the BET analysis, surface areas of 31.082 and 27.113 m2/g were calculated for hematite nanoparticles synthesized with NaOH and NaBH4, respectively, and 45.998, 52.743, and 56.243 m2/g were calculated for maghemite nanoparticles synthesized with leaf extract to precursor ratios of 1:2, 1:1, and 2:1, respectively. The photocatalytic malachite green degradation experiment indicates 98.944, 98.902, and 97.930 % degradation efficiency at the optimized experimental parameters for maghemite nanoparticles synthesized with leaf extract and hematite nanoparticles synthesized with NaBH4 and NaOH, respectively. The degradation of malachite green with the three photocatalysts fits first-order kinetics.
以NaOH、NaBH4和金莲叶提取物为还原剂合成氧化铁纳米颗粒。XRD分析证实,以NaOH和NaBH4为还原剂制备的赤铁矿纳米颗粒具有菱形体结构,平均晶粒尺寸分别为28.2287 nm和21.86575 nm。利用金盏花叶提取物合成的氧化铁纳米颗粒为立方棘状结构的磁赤铁矿,平均晶粒尺寸分别为21.69002、21.09579和19.61541 nm,叶提取物与前驱体的比例分别为1:2、1:1和2:1。FT-IR分析表明,赤铁矿和磁铁矿纳米颗粒形成的Fe-O键分别在460 ~ 550 cm−1和570 cm−1左右。DRS分析的光学带隙能量计算表明,NaOH和NaBH4合成的赤铁矿纳米粒子的间接带隙能量分别为1.32和1.14 eV,直接带隙能量分别为1.62和1.55 eV。在叶提取物与前驱物比例为1:2、1:1和2:1时,间接带隙能分别为1.62、1.57和1.66 eV,直接带隙能分别为2.09、2.09和2.20 eV。TGA-DTA分析证实了用叶提取物合成的磁铁矿纳米颗粒的热稳定性得到了改善。NaOH合成的赤铁矿纳米颗粒在89.95、31.79和650.79 °C处有三个不同的吸热峰,总失重量为27.278 %,而NaBH4在94.25 °C处有一个弱吸热峰。以叶提取物为原料合成的磁铁矿纳米颗粒,在比例为1:1的情况下,最大失重量为8.192 %,三种比例下均未出现吸热峰和放热峰。通过BET分析,NaOH和NaBH4合成的赤铁矿纳米颗粒的比表面积分别为31.082和27.113 m2/g,叶提取物与前体比为1:2、1:1和2:1合成的磁铁矿纳米颗粒的比表面积分别为45.998、52.743和56.243 m2/g。光催化孔雀石绿降解实验表明,在优化的实验参数下,以叶提取物合成的磁赤铁矿和以NaBH4和NaOH合成的赤铁矿的光催化降解效率分别为98.944、98.902和97.930 %。三种光催化剂对孔雀石绿的降解均符合一级动力学。
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引用次数: 0
Radio frequency energy harvesting: A review on progress and development, applications, and sustainability benefits 射频能量收集:进展、发展、应用和可持续效益综述
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-21 DOI: 10.1016/j.mtsust.2025.101291
Muhammed Kallumottakkal , Rizwan A. Farade , Mohammad Jawaid , Mahmoud Al Ahmad , Noor Izzri Abdul Wahab , T.M. Yunus Khan , Abdul Saddique Shaik
Radio Frequency (RF) energy harvesting is a promising approach to convert ambient RF signals into electrical power suitable for low-energy devices. The exponential growth of the Internet of Things (IoT) has made long-term power solutions important research. This review discusses cutting-edge research on RF energy harvesting, particularly antenna design, which is crucial for maximizing energy efficiency. To deliver a structured analysis, antennas are categorized according to their frequency bands, ports, elements, and polarization modes. The performance metrics—gain, bandwidth, efficiency, and size—are evaluated and analysed in light of practical applications such as healthcare, IoT, mobile communication, and wearable systems. A design-application mapping table and wearable health monitoring case study demonstrate the technology's practicality. This review compares recent designs, discusses design trade-offs, analyses application-specific bottlenecks, and addresses issues related to fabrication challenges for body-worn and flexible systems. Moreover, promotes sustainability through decreased battery dependence, autonomous operation, and reduced electronic waste. Finally, outlines existing limitations and future works focusing on power conversion efficiency, bandwidth upgradability, dynamic range, and key controversies and technological breakthroughs. This paper further elaborates its findings to guide future antenna designs and system integration evolution towards sustainable RF energy harvesting applications for next-generation wireless and IoT applications.
射频(RF)能量收集是一种很有前途的方法,可以将环境射频信号转换为适合低能量设备的电能。物联网(IoT)的指数级增长使得长期电源解决方案成为重要的研究课题。本文讨论了射频能量收集的前沿研究,特别是天线设计,这对最大限度地提高能量效率至关重要。为了提供结构化的分析,根据天线的频带、端口、元件和极化模式对其进行分类。性能指标——增益、带宽、效率和尺寸——根据医疗保健、物联网、移动通信和可穿戴系统等实际应用进行评估和分析。设计应用映射表和可穿戴式健康监测案例研究证明了该技术的实用性。这篇综述比较了最近的设计,讨论了设计权衡,分析了特定应用的瓶颈,并解决了与身体磨损和柔性系统制造挑战相关的问题。此外,通过减少对电池的依赖、自主操作和减少电子垃圾,促进可持续发展。最后,概述了现有的限制和未来的工作,重点是功率转换效率,带宽可升级性,动态范围,以及关键争议和技术突破。本文进一步阐述了其研究结果,以指导未来的天线设计和系统集成发展,以实现下一代无线和物联网应用的可持续射频能量收集应用。
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引用次数: 0
Self-reinforced bio-based polyesters: recent progress and prospects 自增强生物基聚酯:最新进展与展望
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-21 DOI: 10.1016/j.mtsust.2025.101290
Pejman Heidarian , Shazed Aziz , Peter Halley , Tony McNally , Ton Peijs , Luigi-Jules Vandi , Russell J. Varley
The environmental impact of traditional petroleum-based plastics has driven the search for sustainable alternatives, with bio-based polyesters emerging as a promising solution. However, these polymers often suffer from insufficient mechanical properties, which limits their applications. To address this, self-reinforcement has been explored as an innovative approach to enhance the performance of bio-based polyesters. This review provides an overview of the recent advancements in self-reinforced bio-based polyesters, focusing on polymers such as poly(lactic acid) (PLA), polyhydroxyalkanoates (PHAs), and poly(butylene succinate) (PBS). Different self-reinforcement techniques, such as electrospinning, melt spinning, and hot compaction are explored for their effectiveness in enhancing tensile strength, modulus, and overall durability. The review also discusses the integration of these materials into applications ranging from packaging to biomedical devices, where biodegradability and mechanical performance are critical. Furthermore, the paper explores the prospects of self-reinforced bio-based polyesters, emphasizing the need for continued innovation in material design and processing techniques to overcome current limitations.
传统石油基塑料对环境的影响促使人们寻找可持续的替代品,生物基聚酯成为一种有前途的解决方案。然而,这些聚合物的机械性能往往不足,这限制了它们的应用。为了解决这个问题,自我强化已经被探索作为一种创新的方法来提高生物基聚酯的性能。本文综述了近年来自增强生物基聚酯的研究进展,重点介绍了聚乳酸(PLA)、聚羟基烷酸酯(pha)和聚丁二酸酯(PBS)等聚合物的研究进展。不同的自增强技术,如静电纺丝,熔体纺丝和热压实,探索其在提高抗拉强度,模量和整体耐久性方面的有效性。这篇综述还讨论了将这些材料整合到从包装到生物医学设备的应用中,其中生物降解性和机械性能是至关重要的。此外,本文探讨了自增强生物基聚酯的前景,强调需要在材料设计和加工技术方面不断创新,以克服当前的局限性。
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引用次数: 0
Sustainable dielectric materials for energy storage: Processing, properties, and performance evaluation 可持续电介质储能材料:加工、性能和性能评价
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-21 DOI: 10.1016/j.mtsust.2025.101281
Kiran Keshyagol , Shivashankarayya Hiremath , H.M. Vishwanatha , Pavan Hiremath
The growing demand for sustainable electrical and electronic technologies has accelerated the search for environmentally benign dielectric materials with high-performance characteristics suited for applications such as electromagnetic shielding, energy storage, and electroactive devices. In this work, a Naturally Extracted Dielectric (NED) material derived from cuttlefish bone was processed via lyophilization and thermal calcination at various temperatures to enhance structural consistency. Structural evolution from aragonite-based calcium carbonate to calcium oxide (CaO) was confirmed through X-ray diffraction (XRD) and Fourier-Transform Infrared (FTIR) spectroscopy. Dielectric behavior and ion transport mechanisms were assessed using Electrochemical Impedance Spectroscopy (EIS). Among all samples, the material calcined at 750 °C (NED-750) demonstrated the best performance, exhibiting strong Maxwell–Wagner interfacial polarization, high permittivity at low-frequency, and a peak DC conductivity of 5.4 × 10−3 S/m. A reduction of 8.2 % in material density with increasing calcination temperature further indicated enhanced porosity and polarization sites. The correlation of structural data with dielectric response establishes a comprehensive framework for evaluating bio-derived ceramics. These results highlight NED as a promising candidate for next-generation, sustainable dielectric energy storage system and electronic device.
对可持续电气和电子技术不断增长的需求加速了对环境友好的介电材料的寻找,这些材料具有适合电磁屏蔽、能量存储和电活性器件等应用的高性能特性。在这项工作中,从墨鱼骨头中提取一种自然提取的介电材料(NED),通过在不同温度下的冻干和热煅烧来处理,以提高结构的一致性。通过x射线衍射(XRD)和傅里叶红外光谱(FTIR)证实了文石基碳酸钙向氧化钙(CaO)的结构演变。利用电化学阻抗谱(EIS)分析了介电行为和离子输运机制。在所有样品中,750 °C煅烧的材料(NED-750)表现出最好的性能,表现出强的麦克斯韦-瓦格纳界面极化,低频高介电常数,峰值直流电导率为5.4 × 10−3 S/m。随着煅烧温度的升高,材料密度降低了8.2 %,进一步表明孔隙率和极化位点的增强。结构数据与介电响应的相关性为评价生物衍生陶瓷建立了一个全面的框架。这些结果突出了NED作为下一代可持续电介质储能系统和电子器件的有前途的候选者。
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引用次数: 0
Hydrogen embrittlement in storage tank materials and welded joints 储罐材料和焊接接头的氢脆
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-20 DOI: 10.1016/j.mtsust.2025.101282
Ammar Elsheikh , Ali Ali , Fadl A. Essa , Mohamed A.E. Omer , Mohamed G. Abou-Ali , Ninshu Ma
Hydrogen embrittlement (HE) poses a significant threat to the structural integrity and long-term reliability of its storage tanks, particularly in welded joints, where microstructural heterogeneities increase susceptibility. This review presents a comprehensive analysis of HE phenomena, emphasizing its critical role in material degradation. The paper begins by outlining the fundamentals of HE, describing how atomic hydrogen infiltrates metallic lattices, leading to loss of ductility and premature failure. Various HE mechanisms, including hydrogen-enhanced decohesion (HEDE), hydrogen-enhanced localized plasticity (HELP), and hydrogen-induced cracking (HIC), are discussed and classified based on their underlying physical principles. The susceptibility of commonly used storage tank materials, such as high-strength steels and aluminum alloys, is evaluated, with a focus on microstructural and compositional factors. Special attention is given to the welded regions, where residual stresses, grain boundary structures, and weld metal (WM) composition play a pivotal role in accelerating HE. The review also highlights key factors influencing HE in welded joints, including hydrogen diffusion pathways, welding processes, and post-weld treatments. Experimental methodologies, such as slow strain rate testing and thermal desorption analysis, are discussed alongside simulation approaches that model hydrogen diffusion and crack propagation. Finally, the paper outlines current mitigation strategies, including material selection, heat treatment, hydrogen barriers, and cathodic protection, offering insights into practical solutions for reducing HE risks in hydrogen storage systems. This review aims to guide future research and inform engineering practices for safer hydrogen infrastructure.
氢脆(HE)对储罐的结构完整性和长期可靠性构成了重大威胁,特别是在焊接接头中,微观组织的不均匀性增加了易感性。本文综述了HE现象的综合分析,强调了其在材料降解中的关键作用。本文首先概述了HE的基本原理,描述了原子氢如何渗入金属晶格,导致延展性丧失和过早失效。不同的HE机制,包括氢增强脱粘(HEDE)、氢增强局部塑性(HELP)和氢致开裂(HIC),根据其潜在的物理原理进行了讨论和分类。对常用的储罐材料,如高强度钢和铝合金的易感性进行了评估,重点是微观组织和成分因素。特别注意的是焊接区域,残余应力,晶界组织和焊缝金属(WM)成分在加速HE中起关键作用。综述还强调了影响焊接接头中HE的关键因素,包括氢扩散途径、焊接工艺和焊后处理。实验方法,如慢应变速率测试和热解吸分析,以及模拟氢扩散和裂纹扩展的模拟方法进行了讨论。最后,本文概述了当前的缓解策略,包括材料选择、热处理、氢屏障和阴极保护,为降低储氢系统中的HE风险提供了切实可行的解决方案。本综述旨在指导未来的研究,并为更安全的氢基础设施的工程实践提供信息。
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引用次数: 0
The use of biobased polymeric materials as membrane technologies for CO2 capture and separation: a review 生物基高分子材料膜技术在CO2捕集与分离中的应用综述
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-17 DOI: 10.1016/j.mtsust.2025.101279
Zahra Maghazeh, Virginia Signorini, Marco Giacinti Baschetti
Bio-based polymers have recently emerged as a promising alternative to conventional materials for carbon dioxide (CO2) separation, offering a sustainable and environmentally friendly approach to mitigating greenhouse gas emissions. This review explores recent advancements in the design and application of bio-based polymeric membranes for CO2 capture, focusing on their structural properties, separation performance, and scalability. The unique characteristics of bio-based polymers, including tunable functional groups, high processability, and biocompatibility, make them highly suitable for selective CO2 separation in various industrial applications, provided that key challenges such as improving permeability-selectivity trade-off and enhancing chemical stability under harsh conditions, are properly addressed. Additionally, the integration of bio-based polymers with other advanced materials, including nanocomposites and hybrid membranes, is examined as a strategy to further enhance separation efficiency. This review provides a comprehensive overview of the current state of bio-based polymers in membrane technologies for CO2 separation, highlighting both their potential and the technical challenges that need to be addressed for large-scale implementation.
生物基聚合物最近成为一种有前途的二氧化碳(CO2)分离传统材料的替代品,为减少温室气体排放提供了一种可持续和环保的方法。本文综述了生物基聚合物CO2捕集膜的设计和应用的最新进展,重点介绍了它们的结构特性、分离性能和可扩展性。生物基聚合物的独特特性,包括可调官能团、高可加工性和生物相容性,使其非常适合于各种工业应用中的选择性CO2分离,前提是适当解决诸如改善渗透性-选择性权衡和增强恶劣条件下的化学稳定性等关键挑战。此外,生物基聚合物与其他先进材料(包括纳米复合材料和杂化膜)的整合也被视为进一步提高分离效率的策略。本文综述了生物基聚合物用于CO2分离膜技术的现状,强调了它们的潜力和大规模实施需要解决的技术挑战。
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引用次数: 0
Tuning overall water dissociation performance in Fe–Ni–Co layered hydroxides via S, P, and B doping: Experimental and theoretical study 通过S, P和B掺杂调整Fe-Ni-Co层状氢氧化物的整体水解离性能:实验和理论研究
IF 7.9 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY Pub Date : 2025-12-17 DOI: 10.1016/j.mtsust.2025.101280
Mohsen Saeidi , Amir Hossein Aghaii , Kaivan Mohammadi , Farzaneh Shayeganfar , Jing Bai , Abdolreza Simchi
Alkaline water electrolysis (AWE) remains limited by sluggish reaction kinetics, high overpotentials, and insufficient catalyst stability. Here, we introduce an engineered hierarchical electrocatalyst in which (B, P, S)-modulated Fe–Ni–Co layered double hydroxides (LDHs) are grown on 3D-printed 316L stainless-steel microarrays with an interface of nickel nanocones (NC) to maximize active surface area and enhance mass transport. Density functional theory indicates that boron substitution at Fe sites balances oxygen-evolution reaction (OER) intermediate binding energies, creating a fully downhill free-energy profile and reducing the OER barrier. Phosphorus incorporation on Ni sites tunes the hydrogen adsorption energy toward near-thermoneutral values, optimizing hydrogen-evolution reaction (HER) kinetics. X-ray photoelectron spectroscopy confirms strong interfacial interactions, reduced oxygen vacancies, and optimized metal–anion bonding, facilitating enhanced charge transfer. The optimized asymmetric electrolyzer delivers 500 mA cm−2 at 1.93 V with Faradaic efficiencies exceeding 79 %, demonstrating a scalable route to efficient and durable AWE.
碱性电解(AWE)仍然受到反应动力学缓慢,高过电位和催化剂稳定性不足的限制。在这里,我们介绍了一种工程级联电催化剂,其中(B, P, S)调制的Fe-Ni-Co层状双氢氧化物(LDHs)生长在3d打印的316L不锈钢微阵列上,该微阵列具有镍纳米锥(NC)界面,以最大化活性表面积并增强质量传输。密度泛函理论表明,Fe位点的硼取代平衡了析氧反应(OER)的中间结合能,形成了一个完全下坡的自由能分布,并降低了OER势垒。磷在Ni位点的结合调整了氢的吸附能接近热中性值,优化了析氢反应动力学。x射线光电子能谱证实了强的界面相互作用,减少了氧空位,优化了金属-阴离子键,促进了电荷转移。优化后的不对称电解槽在1.93 V下输出500 mA cm−2 ,法拉第效率超过79 %,展示了高效和持久的AWE的可扩展路线。
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引用次数: 0
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Materials Today Sustainability
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