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Recent advances of spinel CuCo2O4 in different Structural dimensions (0D-3D) for an electrochemical supercapacitor device: a short research review 用于电化学超级电容器装置的不同结构尺寸(0D-3D)尖晶石钴氧化物的最新研究进展:简短研究综述
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-19 DOI: 10.1016/j.jallcom.2024.177581
V.A. Kadam, V.L. Patil, S.H. Mujawar, A.P. Torane, L.D. Kadam
An electrochemical supercapacitor device that assumes a significant part in gathering sustainable electrical energy to satisfy the need for worldwide energy utilization. The electrode is one of the fundamental parts of a supercapacitor device, sometimes a single material is deficient in satisfying the electrode material requirement. Hence, the researcher’s key challenge is to produce the Binary/Ternary/Quaternary materials and utilize them to fabricate the electrode with a large surface area, novel shape, and controlled dimensions. In this short review, we outline current developments in the design of nanostructured spinel-based CuCo2O4 electrodes in different Structural dimensions such as zero-, one-, two-, and three-dimensions for the application of supercapacitors. The surface area, charge transport efficiency, and overall electrochemical performance of the supercapacitor are all significantly influenced by the dimensionality of the electrode materials. Supercapacitors can have much higher energy and power densities by designing and using materials with the right dimensions. It has been specifically explained how various dimensional architectures relate to the appropriate electrochemical performances, including specific capacitance, rate capability, cycle stability, power density, and energy density, which may serve as a guideline for the next generation of supercapacitor electrode design.
电化学超级电容器装置在收集可持续电能以满足全球能源利用需求方面发挥着重要作用。电极是超级电容器装置的基本组成部分之一,有时单一材料无法满足电极材料的要求。因此,研究人员面临的主要挑战是生产二元/三元/四元材料,并利用它们制造出表面积大、形状新颖、尺寸可控的电极。在这篇简短的综述中,我们概述了目前在设计零维、一维、二维和三维等不同结构尺寸的纳米尖晶石基 CuCo2O4 电极以应用于超级电容器方面的发展情况。超级电容器的表面积、电荷传输效率和整体电化学性能都会受到电极材料尺寸的显著影响。通过设计和使用具有正确尺寸的材料,超级电容器可以获得更高的能量和功率密度。本文具体解释了各种尺寸结构与适当的电化学性能(包括比电容、速率能力、循环稳定性、功率密度和能量密度)之间的关系,可作为下一代超级电容器电极设计的指南。
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引用次数: 0
Effects of strain rate, temperature and microstructure on mechanical properties of (CoCrNi)94Al3Ti3 medium-entropy alloy: Experiments and constitutive modeling 应变率、温度和微观结构对 (CoCrNi)94Al3Ti3 中熵合金机械性能的影响:实验和构成模型
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-19 DOI: 10.1016/j.jallcom.2024.177551
R.C. Pan, C.H. Mi, P.F. Han, N.B. Zhang, Y. Cai, L. Lu, S.N. Luo
Mechanical properties and microstructure evolution of as-cast, solution-treated and aged (CoCrNi)94Al3Ti3 medium-entropy alloys (MEAs) are investigated under uniaxial compression at strain rates from 10−3 to 3700 s−1 within temperatures from 123 to 573 K. Compared to the single-phase solution-treated MEA, spherical nanosized particles result in an increase in the yield stress approximately by 55% (to 586 MPa) and 73% (to 655 MPa) for the as-cast and aged (CoCrNi)94Al3Ti3, respectively. At ambient temperature, the as-cast and aged alloys demonstrate significantly higher dynamic strain rate sensitivity. At a fixed strain rate, the yield strengths and flow stresses increase with decreasing temperature for all three alloys. The as-cast and aged alloys exhibit significantly higher yield strength primarily due to precipitation strengthening of the coherent ordered L12 precipitates. Dislocation slip dominates the plastic deformation and leads to the weak but apparent ⟨110⟩ texture along the loading direction, and no deformation twins are observed in all alloys. Besides, Khan-Liu constitutive models are developed and can well describe the plastic flow of three alloys over a wide range of strain rates and temperatures.
在温度为 123 至 573 K、应变率为 10-3 至 3700 s-1 的单轴压缩条件下,研究了原铸、固溶处理和时效 (CoCrNi)94Al3Ti3 中熵合金 (MEA) 的力学性能和微观结构演变。与单相溶液处理的 MEA 相比,球形纳米颗粒使原铸和老化 (CoCrNi)94Al3Ti3 的屈服应力分别提高了约 55% (达 586 兆帕)和 73%(达 655 兆帕)。在环境温度下,原铸合金和时效合金的动态应变速率灵敏度明显更高。在固定应变速率下,所有三种合金的屈服强度和流动应力都随着温度的降低而增加。原铸合金和时效合金的屈服强度明显更高,这主要是由于相干有序 L12 沉淀的沉淀强化作用。位错滑移在塑性变形中占主导地位,并导致沿加载方向出现微弱但明显的⟨110⟩纹理,所有合金中均未观察到变形孪晶。此外,建立的 Khan-Liu 构成模型可以很好地描述三种合金在宽应变率和温度范围内的塑性流动。
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引用次数: 0
Corrigendum to “Enhancement on mechanical properties via phase separation induced by Cu-added high-entropy alloy fillers in metastable ferrous medium-entropy alloy welds” [J. Alloy. Compd. 1010 (2025) 177321] 更正:"通过在可转移的铁质中熵合金焊缝中添加铜质高熵合金填料诱导相分离来增强机械性能" [J. Alloy. Compd. 1010 (2025) 177321]
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-18 DOI: 10.1016/j.jallcom.2024.177474
Yoona Lee, Seonghoon Yoo, Byungrok Moon, Nokeun Park, Seongmoon Seo, Dongyun Lee, Byeong-Joo Lee, Hyoung Seop Kim, Namhyun Kang
The author regrets the following:<ul><li><span>1)</span><span>I would like to replace the <span><span>Fig. 2</span></span> with the following figure as there is a typo in the original <span><span>Fig. 2</span></span>.<figure><span><img alt="Fig. 2" aria-describedby="cap0005" height="416" src="https://ars.els-cdn.com/content/image/1-s2.0-S0925838824040623-gr1.jpg"/><ol><li><span><span>Download: <span>Download high-res image (520KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span><span><span><p><span>Fig. 2</span>. Weldability and compositional behaviour in GTA welds using CoFeMnNiCu and (CoFeMnNi)<sub>70</sub>Cu<sub>30</sub> fillers: (a) Macroscopical views of the BSE image and (b) compositional behaviours of the cross-sections in transverse GTA welds. Yellow and red dashed lines indicate the fusion line and the location of quantitative EPMA, respectively.</p></span></span></figure></span></li><li><span>2)</span><span>There is a blank space after = in <span><span>Eqs. (2) and (4)</span></span>. The corrected equations are follows:</span></li></ul><span><span><span>(2)</span><span><span style=""></span><span data-mathml='<math xmlns="http://www.w3.org/1998/Math/MathML"><mrow is="true"><mi is="true">&#x3B4;</mi><mo is="true">=</mo><mn is="true">100</mn><msqrt is="true"><munderover is="true"><mo is="true">&#x2211;</mo><mrow is="true"><mi is="true">i</mi><mo is="true">=</mo><mn is="true">1</mn></mrow><mi is="true">n</mi></munderover><msub is="true"><mrow is="true"><mi is="true">C</mi></mrow><mrow is="true"><mi is="true">i</mi></mrow></msub><msup is="true"><mrow is="true"><mfenced open="(" close=")" is="true"><mrow is="true"><mn is="true">1</mn><mo is="true">&#x2212;</mo><mfrac is="true"><mrow is="true"><msub is="true"><mi is="true">r</mi><mi is="true">i</mi></msub></mrow><mrow is="true"><mover accent="true" is="true"><mi is="true">r</mi><mo is="true">&#xAF;</mo></mover></mrow></mfrac></mrow></mfenced></mrow><mn is="true">2</mn></msup></msqrt><mo is="true">,</mo><mspace width="0.25em" is="true" /><mspace width="0.25em" is="true" /><mover accent="true" is="true"><mi is="true">r</mi><mo is="true">&#xAF;</mo></mover><mo is="true">=</mo><munderover is="true"><mo is="true">&#x2211;</mo><mrow is="true"><mi is="true">i</mi><mo is="true">=</mo><mn is="true">1</mn></mrow><mi is="true">n</mi></munderover><msub is="true">&
作者对以下内容表示遗憾:1)由于原图 2 中存在错字,我想用下图替换图 2:下载高清图片 (520KB)Download:下载:下载全尺寸图像图 2.使用 CoFeMnNiCu 和 (CoFeMnNi)70Cu30 填料的 GTA 焊缝的可焊性和成分特性:(a) BSE 图像的宏观视图;(b) 横向 GTA 焊缝截面的成分特性。黄色和红色虚线分别表示熔合线和 EPMA 定量位置。The corrected equations are follows:(2)δ=100∑i=1nCi1−rir¯2,r¯=∑i=1nCiriδ=100∑i=1nCi1−rir¯2,r¯=∑i=1nCiri(4)ρ111=431a2NAρ111=431a2NA
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引用次数: 0
Breaking Barriers: Addressing Challenges in Perovskite Solar Cell Development 打破障碍:应对包光体太阳能电池开发中的挑战
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-18 DOI: 10.1016/j.jallcom.2024.177648
Maria Rani, Muhammad Mohsin Khan, Arshid Numan, Mohammed Khalid, Syed Mustansar Abbas, Mudassir Iqbal, Muhammad Adil Mansoor
Perovskites have captured the interest of researchers for over a decade due to their high-power conversion efficiency (PCE). These materials boast excellent chemical and physical properties, making them ideal for solar cell production. On a small scale, perovskites are synthesized using various methods such as dual-source vapor deposition, one-step and two-step solution deposition, vapor-assisted solution deposition, and sequential deposition techniques. For large-scale production, industries employ techniques like inkjet printing, drop casting, blade coating, slot-die coating, and spray coating. Despite their potential, perovskite solar cells face significant challenges in commercialization, primarily due to chemical stability issues to only a few months. Therefore, recent research focuses on improving film formation and interfacial engineering to enhance device PCE and stability. To move towards commercialization, it is crucial to address degradation caused by environmental factors such as moisture and UV light through material stability improvements such as encapsulation, interface engineering, and humidity control. This necessitates the development of standardized stability tests and optimized conditions for maximum performance. This review aims to delve into the intricacies of perovskite structures and their fabrication techniques on both small and large scales. It also critically examines the challenges and obstacles in commercializing perovskites. Finally, the review offers insights into future strategies for achieving high PCE in perovskite solar cells, emphasizing the need for advanced materials engineering, robust encapsulation techniques, and scalable, cost-effective deposition methods to enhance device stability, moisture resistance, and overall longevity, paving the way for the commercialization of perovskite-based photovoltaics.
近十多年来,透镜材料因其高功率转换效率(PCE)而备受研究人员的关注。这些材料具有优异的化学和物理特性,是生产太阳能电池的理想材料。在小规模生产中,可采用各种方法合成过氧化物晶石,如双源气相沉积、一步法和两步法溶液沉积、气相辅助溶液沉积以及连续沉积技术。在大规模生产方面,工业界采用了喷墨打印、滴铸、叶片镀膜、槽模镀膜和喷涂等技术。尽管包光体太阳能电池潜力巨大,但在商业化方面却面临着巨大的挑战,主要原因是化学稳定性问题,其化学稳定性只能维持几个月。因此,近期的研究重点是改善薄膜形成和界面工程,以提高器件的 PCE 和稳定性。要实现商业化,关键是要通过封装、界面工程和湿度控制等材料稳定性改进措施,解决湿气和紫外线等环境因素造成的降解问题。这就需要开发标准化的稳定性测试和优化条件,以实现最佳性能。本综述旨在深入探讨包晶石结构的复杂性及其小规模和大规模制造技术。本综述还批判性地探讨了在将过氧化物晶体商业化方面所面临的挑战和障碍。最后,这篇综述深入探讨了实现包晶体太阳能电池高 PCE 的未来战略,强调需要先进的材料工程、稳健的封装技术以及可扩展、具有成本效益的沉积方法,以提高器件的稳定性、防潮性和整体使用寿命,从而为基于包晶体的光伏技术的商业化铺平道路。
{"title":"Breaking Barriers: Addressing Challenges in Perovskite Solar Cell Development","authors":"Maria Rani, Muhammad Mohsin Khan, Arshid Numan, Mohammed Khalid, Syed Mustansar Abbas, Mudassir Iqbal, Muhammad Adil Mansoor","doi":"10.1016/j.jallcom.2024.177648","DOIUrl":"https://doi.org/10.1016/j.jallcom.2024.177648","url":null,"abstract":"Perovskites have captured the interest of researchers for over a decade due to their high-power conversion efficiency (PCE). These materials boast excellent chemical and physical properties, making them ideal for solar cell production. On a small scale, perovskites are synthesized using various methods such as dual-source vapor deposition, one-step and two-step solution deposition, vapor-assisted solution deposition, and sequential deposition techniques. For large-scale production, industries employ techniques like inkjet printing, drop casting, blade coating, slot-die coating, and spray coating. Despite their potential, perovskite solar cells face significant challenges in commercialization, primarily due to chemical stability issues to only a few months. Therefore, recent research focuses on improving film formation and interfacial engineering to enhance device PCE and stability. To move towards commercialization, it is crucial to address degradation caused by environmental factors such as moisture and UV light through material stability improvements such as encapsulation, interface engineering, and humidity control. This necessitates the development of standardized stability tests and optimized conditions for maximum performance. This review aims to delve into the intricacies of perovskite structures and their fabrication techniques on both small and large scales. It also critically examines the challenges and obstacles in commercializing perovskites. Finally, the review offers insights into future strategies for achieving high PCE in perovskite solar cells, emphasizing the need for advanced materials engineering, robust encapsulation techniques, and scalable, cost-effective deposition methods to enhance device stability, moisture resistance, and overall longevity, paving the way for the commercialization of perovskite-based photovoltaics.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"109 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142665414","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interface engineering of three-phase NiO-CuO/Fe3O4 heterostructured catalyst for quick hydrogen release from ammonia borane methanolysis 三相 NiO-CuO/Fe3O4 异质结构催化剂的界面工程,用于从氨硼烷甲醇分解中快速释放氢气
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-18 DOI: 10.1016/j.jallcom.2024.177642
Liling Li, Haidong Jiang, Yufa Feng, Jinyun Liao, Hao Li
Catalytic methanolysis of ammonia borane represents a promising technology for in situ hydrogen production. However, the widespread application of this technology is constrained by the prohibitive cost associated with noble metal catalysts. Consequently, the development of cost-effective and robust is essential for commercial scaling of this technology. In this study, a series of NiO-CuO/Fe3O4 catalyst with three-phase interfaces for ammonia borane methanolysis were fabricated by supporting NiO-CuO with Fe3O4. It was demonstrated that the Fe3O4 support in the catalyst could not only modulate the electronic structure of catalyst but also and confer magnetic characteristics upon it. The catalyst bearing a Ni/Cu molar ratio of 2:2 achieved a turnover frequency (TOF) of 13.5 min-1 in ammonia borane methanolysis, along with long-term stability. Furthermore, magnetic characterization confirmed the catalyst’s ferromagnetic properties with a coercivity of 51.8 Oe, facilitating the magnetic separation of the catalyst under an external magnetic field. Through various exhaustive characterizations, it was revealed that abundant interfacial positively charged Ni sites and negatively charged Cu sites in NiO-CuO/Fe3O4 catalyst could activate methanol and ammonia borane, respectively, thus promoting the hydrogen production efficiently. Considering the excellent activity and recyclability of NiO-CuO/Fe3O4, it is anticipated to gain widespread applications in the industrial production of hydrogen from ammonia borane methanolysis.
氨硼烷催化甲醇分解是一种前景广阔的原位制氢技术。然而,由于贵金属催化剂的成本过高,该技术的广泛应用受到限制。因此,开发具有成本效益且坚固耐用的催化剂对于该技术的商业推广至关重要。本研究通过用 Fe3O4 支持 NiO-CuO 制备了一系列具有三相界面的 NiO-CuO/Fe3O4 催化剂,用于氨硼烷甲醇分解。结果表明,催化剂中的 Fe3O4 支承不仅能调节催化剂的电子结构,还能赋予催化剂磁性。镍/铜摩尔比为 2:2 的催化剂在氨硼烷甲醇分解过程中的转化频率(TOF)达到 13.5 min-1,并具有长期稳定性。此外,磁性表征证实了催化剂的铁磁特性,其矫顽力为 51.8 Oe,有助于催化剂在外部磁场下进行磁分离。通过各种详尽的表征发现,NiO-CuO/Fe3O4 催化剂中丰富的界面正电荷 Ni 位点和负电荷 Cu 位点可分别活化甲醇和硼烷氨,从而有效促进制氢。考虑到 NiO-CuO/Fe3O4 的优异活性和可回收性,预计它将在硼烷甲烷氨解制氢的工业生产中得到广泛应用。
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引用次数: 0
Corrigendum to “Heterogeneous alloyed CuSnO-DopaCube mediated photo-Fenton and photothermal synergistic catalysis for dye elimination” [J. Alloy. Compd. 960 (2023) 170737] 对 "异质合金化 CuSnO-DopaCube 介导的染料消除光芬顿和光热协同催化 "的更正 [J. Alloy. Compd.
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-18 DOI: 10.1016/j.jallcom.2024.177599
Jingpi Gao, Qinghao He, Gaofeng Liang, Lingqing Luo, Xiaoran Liu, Kaiyong Cai, Jinghua Li
For the article “Heterogeneous alloyed CuSnO-DopaCube mediated photo-Fenton and photothermal synergistic catalysis for dye elimination, JALCOM-D-23-05291”, the authors apologize to misuse of wrong images that used in Fig. 6B, which ascribed to the unintentional mistake during data typesetting process. The rearranged right figure is shown here below. The authors promise that the error does not influence the final results and conclusions for this manuscript.
Fig. 6
  1. Download: Download high-res image (175KB)
  2. Download: Download full-size image

Fig. 6. B. Detection of ·OH generation through EPR testing.

关于 "Heterogeneous alloyed CuSnO-DopaCube mediated photo-Fenton and photothermal synergistic catalysis for dye elimination, JALCOM-D-23-05291 "一文,作者对图 6B 中使用的错误图片表示歉意,该图片是由于数据排版过程中的无意识错误造成的。重新排列后的右图如下。作者承诺,该错误不会影响本稿件的最终结果和结论:下载高清图片 (175KB)Download:下载全尺寸图像图 6.B. 通过 EPR 测试检测 -OH 的生成。
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引用次数: 0
Self-Powered Solar-Blind Ultraviolet Detectors Based on the Amorphous Boron Nitride Films 基于非晶氮化硼薄膜的自供电太阳能紫外探测器
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-17 DOI: 10.1016/j.jallcom.2024.177635
Cheng Wu, Peiwen Lv, Zhaojie Zhu, Jianfu Li, Chaoyang Tu, Chenlong Chen, G. Lakshminarayana, Hongyan Wang, Yan Wang
Boron nitride (BN) has been a popular material in the field of ultraviolet detection because of its excellent thermal conductivity, high breakdown field strength, high absorption coefficient, and strong resistance to radiation. However, the harsh preparation conditions of its large-scale single crystal films limit the rapid development of its devices. In this work, amorphous BN films were deposited by the magnetron sputtering technique at a relatively low temperatures. On the basis of the films, the asymmetric Schottky junction solar-blind ultraviolet detectors were fabricated by the Ohmic and Schottky contact, respectively. The maximum responsivity and detectivity of the detectors are 6.4 μA/W and 2.5 × 1010 Jones under 20 V bias and 81.1 μW/cm2 ultraviolet light irradiation, respectively. More importantly, the fabricated asymmetric Schottky junction detector also achieves the stable self-powered characteristics due to the presence of its built-in electric field, and the performances are further improved after the rapid thermal annealing. The prepared BN asymmetric Schottky junction detector can operate without the need for the external power supply, which have many advantages such as simplifying the equipment structure and being able to operate in wireless. This work will provide a new reference for the design of the next generation of independent sustainable detectors.
氮化硼(BN)因其优异的热导率、高击穿场强、高吸收系数和强抗辐照性能,一直是紫外探测领域的热门材料。然而,其大规模单晶薄膜的制备条件十分苛刻,限制了其器件的快速发展。在这项工作中,采用磁控溅射技术在相对较低的温度下沉积了非晶 BN 薄膜。在薄膜的基础上,通过欧姆接触和肖特基接触分别制作了非对称肖特基结日光盲紫外探测器。在 20 V 偏置和 81.1 μW/cm2 紫外线照射下,探测器的最大响应率和探测率分别为 6.4 μA/W 和 2.5 × 1010 Jones。更重要的是,由于其内置电场的存在,所制备的非对称肖特基结探测器还实现了稳定的自供电特性,并且在快速热退火后性能进一步提高。制备的 BN 非对称肖特基结探测器无需外接电源即可工作,具有简化设备结构、可无线工作等诸多优点。这项工作将为下一代独立可持续探测器的设计提供新的参考。
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引用次数: 0
Accelerated melting annealing synthesis of high-performance filled skutterudite through repeated quenching 通过反复淬火加速熔融退火合成高性能填充沸石
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-17 DOI: 10.1016/j.jallcom.2024.177547
XuRi Rao, YuanGe Luo, JiangLong Zhu, Xiaobo Tan, Qian Deng, RuiHeng Li, BangZhou Tian, Ran Ang
The melt-annealing method is currently the main method for preparing the skutterudite materials and devices. However, its extensive utilization is impeded by a time-consuming annealing process. To address this issue, we have developed a melt-quenching-annealing-quenching procedure that significantly shortens the annealing time of Yb-filled CoSb3 skutterudite to only 1 day. Our findings confirm that quenching after annealing effectively promotes the formation of CoSb3 phase. Moreover, the reduced annealing time restricts grain growth. This outcome leads to a evident reduction in lattice thermal conductivity, taking into account the effect of the off-center Yb filler in voids distorting the crystal structure. Ultimately, a competitive zT of ∼1.25 is achieved at 823 K in Yb-filled CoSb3. This work provides a guidance for the rapid preparation of skutterudite by melt-annealing.
熔融退火法是目前制备沸石材料和设备的主要方法。然而,耗时的退火过程阻碍了该方法的广泛应用。为解决这一问题,我们开发了一种熔融-淬火-退火-淬火程序,该程序可将镱填充 CoSb3 钙钛矿的退火时间大幅缩短至 1 天。我们的研究结果证实,退火后的淬火能有效促进 CoSb3 相的形成。此外,退火时间的缩短还限制了晶粒的生长。考虑到空隙中偏离中心的镱填料会扭曲晶体结构,这一结果导致晶格热导率明显下降。最终,镱填充 CoSb3 在 823 K 时的 zT 值达到了 1.25。这项研究为通过熔融退火快速制备沸石提供了指导。
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引用次数: 0
Poly(allylamine) and cysteine co-capped silver indium sulfide quantum dots with excellent photostability for specific Cd2+ and Zn2+ detection based on fluorescence enhancement 聚(烯丙胺)和半胱氨酸共封端硫化银铟量子点具有优异的光稳定性,可用于基于荧光增强的 Cd2+ 和 Zn2+ 特异性检测
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-17 DOI: 10.1016/j.jallcom.2024.177631
Jinhong Gong, Xuenong Zhang, Shan Xu, Hao Yang, Kun Yan, Xueyun Sun, Dan Su, Hufeng Fang
Metal chalcogenide quantum dots (MCQDs) have received tremendous attention in biomedical field for their fascinating optical properties and the admirable biomolecular modifiability. However, challenged by low stability and notorious biocompatibility, MCQDs make them limited for direct biomedical use. Herein, a novel designed and synthesized poly(allylamine) and cysteine co-capped silver indium sulfide quantum dots (PAA-Cys-AIS QDs) with excellent photostability is reported for the specific rapid detection of Cd2+ and Zn2+ ions. The obtained water-soluble PAA-Cys-AIS QDs emitted a stable orange fluorescence at 625 nm with an average size of 3.639 ± 1.006 nm. The unusual anti-photobleaching property of PAA-Cys-AIS QDs is demonstrated to be owing to the introducing of poly(allylamine) and cysteine, which uniquely increased the crystallinity and hydrodynamic size of the structure system. Unexpectedly, unlike most reported approaches for Cd2+ and Zn2+ detection based on the quenching fluorescence mechanism, the PAA-Cys-AIS QDs showed remarkable and rapid fluorescence enhancement after being exposed to Cd2+ and Zn2+ ions aqueous solutions. Notably, the detection limits of the new probe for Cd2+ and Zn2+ are 175 and 50 nM respectively. Complexation and metal ions doping mechanisms are proposed to be responsible for the enhancement of photoluminescence intensity based on the metal ions capture capacity coming from PAA-Cys-AIS QDs’ intrinsic defects and abundant surface amino functional groups. Moreover, the intracellular photostability and biocompatibility of PAA-Cys-AIS QDs are strong enough to prompt us to investigate the metal ions imaging applications in SH-SY5Y cells to further demonstrate the potential for real-live biomedical applications.
金属卤化物量子点(MCQDs)因其迷人的光学特性和令人赞叹的生物分子可调控性,在生物医学领域受到极大关注。然而,MCQDs 的低稳定性和众所周知的生物相容性使其在生物医学领域的直接应用受到限制。本文报告了一种新设计和合成的具有优异光稳定性的聚烯胺和半胱氨酸共封端硫化银铟量子点(PAA-Cys-AIS QDs),用于特异性快速检测 Cd2+ 和 Zn2+ 离子。所获得的水溶性 PAA-Cys-AIS QDs 在 625 纳米波长下发出稳定的橙色荧光,平均粒径为 3.639 ± 1.006 纳米。PAA-Cys-AIS QDs 不同寻常的抗光漂白特性被证明是由于引入了聚(烯丙基胺)和半胱氨酸,从而独特地增加了结构体系的结晶度和流体力学尺寸。出乎意料的是,与大多数基于淬灭荧光机制的 Cd2+ 和 Zn2+ 检测方法不同,PAA-Cys-AIS QDs 在暴露于 Cd2+ 和 Zn2+ 离子水溶液后显示出显著而快速的荧光增强。值得注意的是,新探针对 Cd2+ 和 Zn2+ 的检测限分别为 175 nM 和 50 nM。根据 PAA-Cys-AIS QDs 的固有缺陷和丰富的表面氨基官能团所产生的金属离子捕获能力,提出了络合和金属离子掺杂机制是光致发光强度增强的原因。此外,PAA-Cys-AIS QDs 的细胞内光稳定性和生物相容性足以促使我们研究其在 SH-SY5Y 细胞中的金属离子成像应用,以进一步证明其在实际生物医学应用中的潜力。
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引用次数: 0
Microstructure, room-temperature mechanical properties, and oxidation resistance of Ti-added Mo-Si-B alloys fabricated via hot pressing sintering 通过热压烧结制造的添加钛的 Mo-Si-B 合金的微观结构、室温力学性能和抗氧化性
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2024-11-17 DOI: 10.1016/j.jallcom.2024.177634
Xiancong Chen, Cheng Wang, Haijuan Ju, Xiangrong Li, Yi Qu
Microstructure, room-temperature mechanical properties, and oxidation resistance of Mo-12Si-8B-xTi (x = 10, 20, 30, 40, at.%) alloys fabricated via hot pressing sintering are investigated. 10Ti and 20Ti alloys comprise α-Mo + Mo3Si + Mo5SiB2, whereas 30Ti and 40Ti alloys comprise α-Mo + Mo5SiB2 + Ti5Si3. CALPHAD thermodynamic modeling and EDS indicate a significant increase in Ti solubility in α-Mo and Mo5SiB2 phases with higher Ti content, reaching levels of 30–50%. EBSD analysis reveals evident grain coarsening, the average grain size improves from 1.43 to 2.97 μm. HRTEM characterization demonstrates α-Mo/Mo5SiB2 and α-Mo/Ti5Si3 interfaces are both incoherent. 10Ti alloy exhibits the highest flexural strength of 454 MPa and fracture toughness of 9.9 MPa‧m1/2, while minor differences in fracture toughness are observed among 20–40Ti alloys. The combination of adequate α-Mo matrix, appropriate grain size, and brittle intermetallic phases collectively contribute to determining the strength and toughness. Simultaneous thermal analysis and cyclic oxidation show 40Ti alloy offers the best oxidation resistance at 800–1200 °C, because of the protective TiO2‧SiO2 layer generated through selective oxidation of Ti5Si3 and Ti/Si. Using Pilling-Bedworth ratio as the sole criterion to assess the oxidation resistance is inadequate, as temperature and phase constitution must be considered.
研究了通过热压烧结制造的 Mo-12Si-8B-xTi(x = 10、20、30、40、at.%)合金的微观结构、室温机械性能和抗氧化性。10Ti 和 20Ti 合金由 α-Mo + Mo3Si + Mo5SiB2 组成,而 30Ti 和 40Ti 合金由 α-Mo + Mo5SiB2 + Ti5Si3 组成。CALPHAD 热力学建模和 EDS 显示,随着钛含量的增加,钛在α-Mo 和 Mo5SiB2 相中的溶解度显著增加,达到 30-50% 的水平。EBSD 分析显示出明显的晶粒粗化,平均晶粒尺寸从 1.43 微米提高到 2.97 微米。HRTEM 表征显示,α-Mo/Mo5SiB2 和 α-Mo/Ti5Si3 界面都不连贯。10Ti 合金的抗弯强度最高,为 454 兆帕,断裂韧性为 9.9 兆帕‧米1/2,而 20-40Ti 合金的断裂韧性差异较小。足够的 α-Mo 基体、适当的晶粒尺寸和脆性金属间相共同决定了合金的强度和韧性。同时进行的热分析和循环氧化表明,由于 Ti5Si3 和 Ti/Si 的选择性氧化产生了 TiO2‧SiO2 保护层,40Ti 合金在 800-1200 ℃ 下具有最佳的抗氧化性。将 Pilling-Bedworth 比率作为评估抗氧化性的唯一标准是不够的,还必须考虑温度和相构成。
{"title":"Microstructure, room-temperature mechanical properties, and oxidation resistance of Ti-added Mo-Si-B alloys fabricated via hot pressing sintering","authors":"Xiancong Chen, Cheng Wang, Haijuan Ju, Xiangrong Li, Yi Qu","doi":"10.1016/j.jallcom.2024.177634","DOIUrl":"https://doi.org/10.1016/j.jallcom.2024.177634","url":null,"abstract":"Microstructure, room-temperature mechanical properties, and oxidation resistance of Mo-12Si-8B-<em>x</em>Ti (<em>x</em> = 10, 20, 30, 40, at.%) alloys fabricated via hot pressing sintering are investigated. 10Ti and 20Ti alloys comprise α-Mo + Mo<sub>3</sub>Si + Mo<sub>5</sub>SiB<sub>2</sub>, whereas 30Ti and 40Ti alloys comprise α-Mo + Mo<sub>5</sub>SiB<sub>2</sub> + Ti<sub>5</sub>Si<sub>3</sub>. CALPHAD thermodynamic modeling and EDS indicate a significant increase in Ti solubility in α-Mo and Mo<sub>5</sub>SiB<sub>2</sub> phases with higher Ti content, reaching levels of 30–50%. EBSD analysis reveals evident grain coarsening, the average grain size improves from 1.43 to 2.97 μm. HRTEM characterization demonstrates α-Mo/Mo<sub>5</sub>SiB<sub>2</sub> and α-Mo/Ti<sub>5</sub>Si<sub>3</sub> interfaces are both incoherent. 10Ti alloy exhibits the highest flexural strength of 454<!-- --> <!-- -->MPa and fracture toughness of 9.9<!-- --> <!-- -->MPa‧m<sup>1/2</sup>, while minor differences in fracture toughness are observed among 20–40Ti alloys. The combination of adequate α-Mo matrix, appropriate grain size, and brittle intermetallic phases collectively contribute to determining the strength and toughness. Simultaneous thermal analysis and cyclic oxidation show 40Ti alloy offers the best oxidation resistance at 800–1200 °C, because of the protective TiO<sub>2</sub>‧SiO<sub>2</sub> layer generated through selective oxidation of Ti<sub>5</sub>Si<sub>3</sub> and Ti/Si. Using Pilling-Bedworth ratio as the sole criterion to assess the oxidation resistance is inadequate, as temperature and phase constitution must be considered.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"46 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2024-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142665412","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Journal of Alloys and Compounds
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