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Exploring the progression of energy storage toward flexibility: Metal-organic framework and conducting polymer aspects 探索柔性储能的进展:金属有机框架和导电聚合物方面
Pub Date : 2023-10-01 DOI: 10.1016/j.apmt.2023.101906
Junaid Khan, Ayesha Khan, Bibi Rubab, Fatima Jamshaid, Abdullah A. Al-Kahtani, A. Dahshan
Emerging as cutting-edge technology, flexible supercapacitors (Sc) own great potential toward advancement in state of the art in elastic and wearable electronics. The Sc leads the way as a potential candidate as compared to rechargeable batteries (Low power density, flexibility deficient, igneous as well as toxic nature) because of high power and tunable energy densities, affordability, outstanding cyclic performance, and adaptability. Metal organic frameworks (MOFs) and conducting polymers (CNDPs) are the most fascinating and extensively used electrode materials in flexible assemblies. The structural adaptability, sustainable surface area, three-dimensional porous architecture, and dominant permeability toward additives attribute the MOFs as innovative candidates for flexible electrodes. Likewise, CNDPs contains outstanding specific redox active capacity and inherent elastic polymeric nature, working as supreme pseudo capacitive constituents for the basis of flexible energy storage devices. Although, both materials have various advantages yet certain challenges like the low conductive nature of pristine MOFs and the substandard flexible performance of CNDPs still needs consideration. In addition, a better understanding must be developed to clarify the impacts of recent development and insights that might be used to direct future prospects. This review depicts the current progression toward the structuration of flexible supercapacitors based on MOFs, CNDPs, and their composites. The highlights of current advancement and residual challenges have been presented along with the comparison of hybridization strategies, and analysis of results obtained with directions toward future prospects of flexible supercapacitor.
柔性超级电容器(Sc)作为一种新兴的尖端技术,在弹性和可穿戴电子产品领域具有巨大的发展潜力。与可充电电池(低功率密度、灵活性不足、火成岩和有毒)相比,Sc具有高功率和可调能量密度、可负担性、出色的循环性能和适应性,是一种潜在的候选电池。金属有机骨架(mof)和导电聚合物(CNDPs)是柔性组件中应用最广泛的电极材料。mof具有结构适应性、可持续性表面积、三维多孔结构和对添加剂的渗透性优势,是柔性电极的创新候选材料。同样,CNDPs具有出色的特定氧化还原活性容量和固有的弹性聚合物性质,可以作为柔性储能设备基础的最高伪电容成分。尽管这两种材料都有各自的优点,但仍存在一些挑战,如原始mof的低导电性和cndp的不合格的柔性性能,仍然需要考虑。此外,必须有更好的了解,以澄清最近的发展和可能用于指导未来前景的见解的影响。本文综述了基于mof、cndp及其复合材料的柔性超级电容器结构的最新进展。介绍了柔性超级电容器的研究进展和存在的问题,并对不同的杂交策略进行了比较,分析了结果,对柔性超级电容器的发展前景进行了展望。
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引用次数: 0
Expression of concern: Emerging two-dimensional materials-enabled diagnosis and treatments of Alzheimer's disease: Status and future challenges 关注表达:新兴二维材料支持阿尔茨海默病的诊断和治疗:现状和未来的挑战
Pub Date : 2023-10-01 DOI: 10.1016/j.apmt.2023.101889
None  
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引用次数: 0
Lipase-powered asymmetric silica nanomotors with a tailored head-tail structure for enhanced mucus penetration 脂酶驱动的不对称二氧化硅纳米马达,具有量身定制的首尾结构,可增强粘液穿透性
Pub Date : 2023-10-01 DOI: 10.1016/j.apmt.2023.101916
Wenhuang Ban, Jingjing Qu, Larry Cai, Jianye Fu, Weixi Wu, Hao Song, Chengzhong Yu, Jie Tang
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引用次数: 0
Review and proposition for model-based multivariable-multiobjective optimisation of extrusion-based bioprinting 基于模型的挤出生物打印多变量多目标优化研究综述与展望
Pub Date : 2023-10-01 DOI: 10.1016/j.apmt.2023.101914
Samuel Emebu, Raphael Olabanji Ogunleye, Eva Achbergerová, Lenka Vítková, Petr Ponížil, Clara Mendoza Martinez
Consequent to the development of bioprinting technologies for biomedical applications, especially in tissue engineering, a comprehensive review of extrusion-based bioprinting (EBB) has been written. The review was executed in a manner that laid a foundation for effective optimisation strategies to improve the print resolution or shape fidelity and cell viability of EBB through bioink. However, before achieving this aim the shearing characteristic of the bioink (i.e., shear-thinning or thickening) was described by the Ostwald-de Waele and Herschel-Bulkley models, among other reported models. The dependence of bioink shearing characteristics on temperature and time was also discussed. Emphasis on how these dependencies can be influenced by cross‐linking of bioink molecules was further highlighted, which can be covalent (chemical‐, photo‐cross-linking, etc.) or noncovalent (physical cross‐linking, host‐guest inclusion, ionic interaction, etc.). Models from literature that can physically describe print resolution and cell viability in EBB were discussed and compared. Therefore, multivariable‐multiobjective optimisation strategies were proposed with these models.
随着生物医学应用的生物打印技术的发展,特别是在组织工程方面,对基于挤出的生物打印(EBB)进行了全面的综述。该审查的执行方式为有效的优化策略奠定了基础,从而通过生物链接提高EBB的打印分辨率或形状保真度和细胞活力。然而,在实现这一目标之前,生物链的剪切特性(即剪切变薄或增厚)是由Ostwald-de Waele和Herschel-Bulkley模型以及其他已报道的模型描述的。讨论了温度和时间对生物链剪切特性的影响。进一步强调了这些依赖关系如何受到生物链接分子交联的影响,这可以是共价的(化学、光交联等)或非共价的(物理交联、主客体包合、离子相互作用等)。从文献中可以物理描述打印分辨率和细胞活力的模型进行了讨论和比较。因此,利用这些模型提出了多变量-多目标优化策略。
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引用次数: 0
Hierarchical isoporous membrane filters for simultaneous reduction of pressure drop and efficient removal of nanoscale airborne contaminants 分级等孔膜过滤器同时减少压力降和有效去除纳米级空气污染物
Pub Date : 2023-08-01 DOI: 10.1016/j.apmt.2023.101856
Him Cheng Wong, Shi Ke Ong, Erik Birgersson, Mei Chee Tan, Hong Yee Low
Isoporous membranes with well-defined pore architectures offer a unique design approach to achieve a multi-scale porous network. For instance, isoporous membranes with progressively smaller pore sizes can be stacked to create a hierarchical pore network in which each length scale and the gradient of the pore network are deterministic by design. In this paper, we introduce a hierarchically-arranged multilayer isoporous air filter that comprises an ultrathin (thickness <1μm) nanoporous active filtration layer and a microporous support layer. To maximize airflow and thereby reduce pressure drop across the membrane, we engineered a gap between the nanoporous and microporous membranes by designing and fabricating microscale spacer structures akin to feed spacers used in spiral wound reverse osmosis membranes. We demonstrated that such hierarchical isoporous membranes with integrated spacers (HIM-S) can retain high filtration efficiency (>95%) for ultrafine, most penetrating particle size (MPPS) while simultaneously reducing the pressure drop across the membrane (by ∼86%).
具有明确孔隙结构的等孔膜提供了一种独特的设计方法来实现多尺度多孔网络。例如,孔径逐渐变小的等孔膜可以堆叠起来,形成分层的孔隙网络,其中每个长度尺度和孔隙网络的梯度都是设计确定的。在本文中,我们介绍了一种分层排列的多层等孔空气过滤器,该过滤器包括超薄(厚度95%),用于超细,穿透性最强的粒径(MPPS),同时降低了膜上的压降(约86%)。
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引用次数: 0
The impact of surface scratches on the corrosion behavior of nanocrystalline high entropy alloy coatings: Electrochemical experiments and first-principles study 表面划痕对纳米晶高熵合金涂层腐蚀行为的影响:电化学实验和第一性原理研究
Pub Date : 2023-04-01 DOI: 10.1016/j.apmt.2023.101767
Shuang Peng, Jiang Xu, Dongsheng Hu, Zong-Han Xie, Paul Munroe
To prolong the service life of engineering components used in aggressive environments, a TiZrHfMoW refractory high entropy alloy (RHEA) coating was prepared onto a titanium alloy substrate. Various electrochemical analytical techniques were used to evaluate the corrosion resistance of the scratched RHEA coating in a 3.5 wt.% NaCl solution. The electrochemical corrosion tests indicate that the scratched RHEA coating exhibits a higher electrochemical stability and a lower corrosion rate than the bare titanium alloy. The effects of the localized plastic deformation on the corrosion behavior for the RHEA coating was investigated. A slab model for the RHEA surface was proposed for the first-principles calculation to explored the change of the electron work function (EWF) as a function of external stress. The influence of the constituent elements in the RHEA on the mechanical properties and the electron work function was study to uncover the mechanism underlying the high scratch corrosion resistance of the RHEA coating and provide guidance for the composition design of refractory high entropy alloy.
为了延长恶劣环境下工程部件的使用寿命,在钛合金基体上制备了TiZrHfMoW耐火高熵合金(RHEA)涂层。采用多种电化学分析技术评价了划痕涂层在3.5 wt.% NaCl溶液中的耐蚀性。电化学腐蚀试验表明,与裸钛合金相比,刮痕涂层具有更高的电化学稳定性和更低的腐蚀速率。研究了局部塑性变形对涂层腐蚀行为的影响。提出了一种用于第一性原理计算的平板模型,探讨了电子功函数(EWF)随外加应力的变化规律。研究了RHEA中组成元素对其力学性能和电子功函数的影响,揭示了RHEA涂层耐划伤腐蚀的机理,为耐火高熵合金的成分设计提供指导。
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引用次数: 1
Applied current on the suppression of strontium segregation in Sr2Fe1.5Mo0.5O6-δ electrode for improved oxygen evolution reaction 施加电流抑制Sr2Fe1.5Mo0.5O6-δ电极上的锶偏析以改善析氧反应
Pub Date : 2023-04-01 DOI: 10.1016/j.apmt.2023.101769
Hao-Yang Li, Pei-Chen Su
Strontium surface segregation is the main issue that causes long-term performance degradation in strontium-containing electrodes for solid oxide electrolysis cells. In this research, we effectively suppress strontium segregation by applying an anodic current that drives the segregated strontium back to the perovskite lattice and mitigate electrode performance degradation. By monitoring the impedance of Sr2Fe1.5Mo0.5O6-δ (SFM) air electrode under open circuit voltage at high temperature with changing current densities over time, the degradation caused by strontium segregation is verified. The applied current successfully prevent the polarization resistance from increasing is observed. The cell with 0.8 A/cm2 of the applied current increase only 3% of polarization resistance as compared to the cell without applied current after testing at 800 ℃ for 24 h. The atomic ratio of strontium on the SFM electrode surface shows lower strontium content after undergoing applied current, which means that the strontium is indeed migrated back to perovskite lattice under the applied current and result in slower degradation of the SFM electrode.
锶表面偏析是导致固体氧化物电解电池含锶电极长期性能下降的主要问题。在这项研究中,我们通过施加阳极电流,将分离的锶驱动回钙钛矿晶格,有效地抑制了锶的偏析,并减轻了电极性能的下降。通过监测Sr2Fe1.5Mo0.5O6-δ (SFM)空气电极在高温开路电压下电流密度随时间变化的阻抗,验证了锶偏析引起的降解。所施加的电流成功地阻止了极化电阻的增加。当外加电流为0.8 A/cm2时,经过800℃24 h的测试,电池极化电阻仅比未外加电流时增加3%。SFM电极表面的锶原子比显示,在外加电流作用下,锶确实迁移回钙钛矿晶格,导致SFM电极降解较慢。
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引用次数: 0
Self-biomineralized in situ injectable CaSO4 nanorods-enriched collagen-hyaluronic acid composite hydrogels for biomimetic bone reconstruction in a minimally invasive manner 自生物矿化原位注射富含CaSO4纳米棒的胶原-透明质酸复合水凝胶用于微创方式的仿生骨重建
Pub Date : 2023-02-01 DOI: 10.1016/j.apmt.2022.101693
Xingzhu Liu, Yajie Zhang, Zahid Hussain, Penghui Zheng, Mingsheng Xu, Hongbo Zhao, Yuanshan Liu, Yi Cao, Ismat Ullah, Akiyoshi Osaka, Renjun Pei
In situ injectable natural polymer-based hydrogels can be utilized to fill irregular defects and promote tissue regeneration. However, most hydrogels showed limited ability for self-biomineralization and can not guide the formation of new bone. Herein, according to the challenges encountered in advancing materials to clinical research, an injectable collagen-hyaluronic acid (Col-HA) hydrogel embedded with calcium sulfate nanorods (CSN) was developed via a bio-orthogonal reaction between norbornene (Nb) and tetrazine (Tz). The formulated [email protected] composite hydrogels not only have the potential to enhance cell adhesion and proliferation, but also serve as the system to control Ca2+ release. This composite hydrogel displayed impressive injectability, allowing straightforward in situ injection and subsequent adaption of composite hydrogels to irregularly shaped bone defects. CSN-incorporated composite hydrogels facilitate self-biomineralization, thereby fast-forming bone-like hydroxyapatite (HAp) within the hydrogel. Furthermore, Ca2+ released in a steady and sustained way from the composite hydrogels stimulated the differentiation of preosteoblasts, and promoted in situ bone growth. Our findings suggested that [email protected] composite hydrogels can successfully mediate the optimized CSN degradation, effectively accelerate HAp formation, and boost in situ bone development via the minimally invasive application.
可原位注射的天然聚合物基水凝胶可用于填充不规则缺陷和促进组织再生。然而,大多数水凝胶的自我生物矿化能力有限,不能引导新骨的形成。本文针对将材料推进到临床研究中所遇到的挑战,通过降冰片烯(Nb)和四嗪(Tz)的生物正交反应,开发了一种嵌入硫酸钙纳米棒(CSN)的可注射胶原-透明质酸(Col-HA)水凝胶。配制的复合水凝胶不仅具有增强细胞粘附和增殖的潜力,而且还可以作为控制Ca2+释放的系统。这种复合水凝胶表现出令人印象深刻的注射性,允许直接原位注射和随后的复合水凝胶适应不规则形状的骨缺陷。csn掺入的复合水凝胶促进自生物矿化,从而在水凝胶内快速形成骨样羟基磷灰石(HAp)。此外,复合水凝胶稳定持续地释放Ca2+,刺激成骨前细胞的分化,促进原位骨生长。我们的研究结果表明,复合水凝胶可以通过微创应用成功介导优化后的CSN降解,有效加速HAp的形成,促进原位骨发育。
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引用次数: 0
Nitrogen and Boron Dual-Doped Graphene Quantum Dots for Near-Infrared Second Window Imaging and Photothermal Therapy. 用于近红外第二窗口成像和光热治疗的氮和硼双掺杂石墨烯量子点。
Pub Date : 2019-03-01 Epub Date: 2018-12-06 DOI: 10.1016/j.apmt.2018.11.011
Hui Wang, Qingxin Mu, Kui Wang, Richard A Revia, Charles Yen, Xinyu Gu, Bowei Tian, Jun Liu, Miqin Zhang

Fluorescence imaging of biological systems in the second near-infrared window (NIR-II) has recently drawn much attention because of its negligible background noise of autofluorescence and low tissue scattering. Here we present a new NIR-II fluorescent agent, graphene quantum dots dual-doped with both nitrogen and boron (N-B-GQDs). N-B-GQDs have an ultra-small size (~ 5 nm), are highly stable in serum, and demonstrate a peak fluorescent emission at 1000 nm and high photostability. In addition to the NIR-II imaging capability, N-B-GQDs efficiently absorb and convert NIR light into heat when irradiated by an external NIR source, demonstrating a photothermal therapeutic effect that kills cancer cells in vitro and completely suppresses tumor growth in a glioma xenograft mouse model. N-B-GQDs demonstrate a safe profile, prolonged blood half-life, and rapid excretion in mice, which are the characteristics favorable for in vivo biomedical applications.

生物系统在第二近红外窗口(NIR-II)中的荧光成像由于其可忽略的自发荧光背景噪声和低组织散射而引起了人们的广泛关注。在这里,我们提出了一种新的NIR-II荧光剂,即氮和硼双重掺杂的石墨烯量子点(N-B-GQDs)。N-B-GQDs具有超小尺寸(~5nm),在血清中高度稳定,并在1000nm处表现出峰值荧光发射和高光稳定性。除了NIR-II成像能力外,N-B-GQD在被外部NIR源照射时有效地吸收NIR光并将其转化为热,在神经胶质瘤异种移植小鼠模型中表现出在体外杀死癌症细胞并完全抑制肿瘤生长的光热治疗效果。N-B-GQDs在小鼠中表现出安全性、延长血液半衰期和快速排泄,这是有利于体内生物医学应用的特征。
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引用次数: 0
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Applied materials today
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