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The incorporation of cocatalyst cobalt sulfide into graphitic carbon nitride: Boosted photocatalytic hydrogen evolution performance and mechanism exploration 助催化剂硫化钴掺入石墨氮化碳:提升光催化析氢性能及机理探索
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-06-01 DOI: 10.1016/j.nanoms.2022.03.001
Zhangqian Liang , Yanjun Xue , Xinyu Wang , Xiaoli Zhang , Jian Tian , Hongzhi Cui

2D-layered graphitic carbon nitride (g-C3N4) is regarded as a great prospect as a photocatalyst for H2 generation. However, g-C3N4's photocatalytic hydrogen evolution (HER) activity is significantly restricted by the recombination of photocarriers. We find that cobalt sulfide (CoS2) as a cocatalyst can promote g-C3N4 nanosheets (NSs) to realize very efficient photocatalytic H2 generation. The prepared CoS2/g-C3N4 hybrids display highly boosted photocatalytic H2 generation performance and outstanding cycle stability. The optimized 7%-CoS2/g-C3N4 hybrids show a much improved photocatalytic H2 generation rate of 36.2 ​μmol−1 ​h−1, which is about 180 times as much as bare g-C3N4 (0.2 ​μmol−1 ​h−1). In addition, the apparent quantum efficiency (AQE) of all the samples was computed under light at λ=370 ​nm, in which the AQE of 7%-CoS2/g-C3N4 hybrids is up to 5.72%. The experimental data and the DFT calculation suggest that the CoS2/g-C3N4 hybrid's excellent HER activity is attributable to the lower overpotential and the smaller Co-H bond activation energy for HER. Accordingly, the CoS2 cocatalyst loading effectively boosts the photocatalytic performance of g-C3N4 for H2 evolution. The project promotes fast development of high-efficiency photocatalysts and low-cost for photocatalytic H2 generation.

二维层状石墨氮化碳(g-C3N4)被认为是一种很有前途的H2生成光催化剂。然而,g-C3N4的光催化析氢(HER)活性受到光载流子复合的显著限制。我们发现,硫化钴(CoS2)作为助催化剂可以促进g-C3N4纳米片(NSs)实现非常有效的光催化制氢。所制备的CoS2/g-C3N4杂化物显示出高度提高的光催化制氢性能和优异的循环稳定性。优化后的7%-CoS2/g-C3N4杂化物的光催化产氢率大大提高,达到36.2​μmol−1​h−1,大约是裸露g-C3N4的180倍(0.2​μmol−1​h−1)。此外,在λ=370的光照下计算了所有样品的表观量子效率(AQE)​实验数据和DFT计算表明,CoS2/g-C3N4杂化物优异的HER活性归因于其较低的过电位和较小的Co-H键活化能。因此,CoS2助催化剂负载有效地提高了g-C3N4对析氢的光催化性能。该项目促进了高效光催化剂和低成本光催化制氢的快速发展。
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引用次数: 7
Cathode host engineering for non-lithium (Na, K and Mg) sulfur/selenium batteries: A state-of-the-art review 非锂(Na、K和Mg)硫/硒电池的阴极主体工程:最新进展
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-06-01 DOI: 10.1016/j.nanoms.2022.01.001
Tingting Yang , Yubin Niu , Qi Liu , Maowen Xu

Sulfur and selenium have been paid more and more attention in energy storage systems because of their high theoretical specific gravimetric and volumetric capacities. With the increasing scarcity of lithium resources, secondary batteries made of sulfur and selenium coupled with other alkali metal/alkaline earth metals (e.g. Na, K, Mg) are expected to play a vital role in future production and human life. Due to the volume expansion, poor conductivity and shuttle effect, the structure design of cathode, as one of the important roles in metal-S/Se batteries, has always been a hot and difficult point. In the review, various host materials of S and Se are clarified and discussed. Typically, carbonaceous materials are the most widely used hosts, while polar materials are becoming more and more popular in metal-S/Se batteries. Through a comprehensive overview, it is hoped that previous research experiences can provide further reference and guidance for the sustainable development of metal-S/Se batteries.

硫和硒由于具有较高的理论比重和体积容量,在储能系统中越来越受到重视。随着锂资源的日益稀缺,由硫和硒与其他碱金属/碱土金属(如Na、K、Mg)制成的二次电池有望在未来的生产和人类生活中发挥至关重要的作用。阴极作为金属硫硒电池的重要组成部分之一,由于其体积膨胀、导电性差和穿梭效应,其结构设计一直是研究的热点和难点。在综述中,对S和Se的各种宿主材料进行了澄清和讨论。通常,碳质材料是最广泛使用的主体,而极性材料在金属-S/Se电池中越来越受欢迎。通过全面综述,希望以往的研究经验能为金属硫硒电池的可持续发展提供进一步的参考和指导。
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引用次数: 7
Stable yellow light emission from lead-free copper halides single crystals for visible light communication 用于可见光通信的无铅卤化铜单晶的稳定黄光发射
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-03-01 DOI: 10.1016/j.nanoms.2022.03.003
Baiqian Wang , Yuru Tang , Xin Yang , Wensi Cai , Ru Li , Wen Ma , Shuangyi Zhao , Chen Chen , Zhigang Zang

Yellow light-emitting diodes (LEDs) as soft light have attracted abundant attention in lithography room, museum and art gallery. However, the development of efficient yellow LEDs lags behind green and blue LEDs, and the available perovskites yellow LEDs suffer from the instability. Herein, a pressure-assisted cooling method is proposed to grow lead-free CsCu2I3 single crystals, which possess uniform surface morphology and enhanced photoluminescence quantum yield (PLQY) stability, with only 10% PLQY losses after being stored in air after 5000 ​h. Then, the single crystals used for yellow LEDs without encapsulation exhibit a decent Correlated Color Temperature (CCT) of 4290 ​K, a Commission Internationale de l'Eclairage (CIE) coordinate of (0.38, 0.41), and an excellent 570-h operating stability under heating temperature of 100 ​°C. Finally, the yellow LEDs facilitate the application in wireless visible light communication (VLC), which show a −3 dB bandwidth of 21.5 ​MHz and a high achievable data rate of 219.2 Mbps by using orthogonal frequency division multiplexing (OFDM) modulation with adaptive bit loading. The present work not only promotes the development of lead-free single crystals, but also inspires the potential of CsCu2I3 in the field of yellow illumination and wireless VLC.

黄色发光二极管(LED)作为一种柔和的光,在光刻室、博物馆和美术馆引起了广泛的关注。然而,高效黄色LED的发展落后于绿色和蓝色LED,并且可用的钙钛矿黄色LED存在不稳定性。本文提出了一种压力辅助冷却方法来生长无铅CsCu2I3单晶,该单晶具有均匀的表面形貌和增强的光致发光量子产率(PLQY)稳定性,在空气中储存5000年后PLQY损失仅为10%​h.然后,用于没有封装的黄色LED的单晶表现出4290的良好的相关色温(CCT)​K、 国际照明委员会(CIE)坐标为(0.38,0.41),在100的加热温度下具有出色的570-h操作稳定性​°C。最后,黄色LED有助于无线可见光通信(VLC)的应用,其带宽为−3 dB,为21.5​MHz和219.2Mbps的高可实现数据速率。本工作不仅促进了无铅单晶的发展,而且激发了CsCu2I3在黄色照明和无线VLC领域的潜力。
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引用次数: 6
Seasoning Chinese cooking pans: The nanoscience behind the Kitchen God's blessing 给中国烹饪锅调味:灶神祝福背后的纳米科学
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-03-01 DOI: 10.1016/j.nanoms.2020.06.001
Chenxi Gao , Na Yang , Cunpu Li , Xi Wang , Xun Yu , Ling Zhang , Zidong Wei

The Chinese iron pan can function as a nonstick pan even without a polytetrafluoroethylene (PTFE) coating after a “Kitchen God blessing” seasoning process. We simulate this process and disclose the science behind the “Kitchen God blessing,” finding that through repeated oil-coating and heating, the reversible insertion and extraction of oxygen atoms split the surface of the iron pan, gradually producing Fe3O4 nanoballs. These balls give the iron pan a conditional hydrophobicity property, meaning the pan would be hydrophilic when the ingredients contain much water and hydrophobic when they contain less water. The former enables heat to be transferred rapidly through the nanoballs while the latter slows down the heat transference and prevents the pan from sticking. This discovery provides an approach of generating nanoballs on the surface of the metal and also discloses the secret of the fantastic taste produced by cooking with a Chinese iron pan.

经过“灶神保佑”的调味过程,即使没有聚四氟乙烯(PTFE)涂层,中国铁锅也可以起到不粘锅的作用。我们模拟了这一过程,揭示了“灶神保佑”背后的科学,发现通过反复涂油和加热,氧原子的可逆插入和提取分裂了铁锅表面,逐渐产生了Fe3O4纳米球。这些球使铁锅具有条件疏水性,这意味着当成分含有大量水时,铁锅将是亲水的,而当成分含有较少水时,则是疏水的。前者使热量能够通过纳米球快速传递,而后者减缓了热量传递并防止锅粘在一起。这一发现提供了一种在金属表面产生纳米球的方法,也揭示了用中国铁锅烹饪产生美妙味道的秘密。
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引用次数: 0
Recent advances in electrocatalysts for seawater splitting 海水裂解电催化剂研究进展
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-03-01 DOI: 10.1016/j.nanoms.2020.12.003
Guangbo Liu, Yingshuang Xu, Teng Yang, Luhua Jiang

Water splitting is an effective strategy to produce renewable and sustainable hydrogen energy. Especially, seawater splitting, avoiding use of the limited freshwater resource, is more intriguing. Nowadays, electrocatalysts explored for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) using natural seawater or saline electrolyte have been increasingly reported. To better understand the current status and challenges of the electrocatalysts for HER and OER from seawater, we comprehensively review the recent advances in electrocatalysts for seawater splitting. The fundamentals, challenges and possible strategies for seawater splitting are firstly presented. Then, the recently reported electrocatalysts that explored for HER and OER from seawater are summarized and discussed. Finally, the perspectives in the development of high-efficient electrocatalysts for seawater splitting are also proposed.

水分解是生产可再生和可持续氢能的有效策略。特别是,海水分解,避免使用有限的淡水资源,更有趣。如今,使用天然海水或盐水电解质探索用于析氢反应(HER)和析氧反应(OER)的电催化剂的报道越来越多。为了更好地了解海水HER和OER电催化剂的现状和挑战,我们全面综述了海水裂解电催化剂的最新进展。首先介绍了海水分解的基本原理、挑战和可能的策略。然后,总结和讨论了最近报道的从海水中探索HER和OER的电催化剂。最后,对开发高效海水裂解电催化剂的前景进行了展望。
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引用次数: 58
Two−dimensional nanomaterials confined single atoms: New opportunities for environmental remediation 限制单原子的二维纳米材料:环境修复的新机遇
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-03-01 DOI: 10.1016/j.nanoms.2022.07.001
Yu Yin , Lei Shi , Shu Zhang , Xiaoguang Duan , Jinqiang Zhang , Hongqi Sun , Shaobin Wang

Two−dimensional (2D) supports confined single−atom catalysts (2D SACs) with unique geometric and electronic structures have been attractive candidates in different catalytic applications, such as energy conversion and storage, value−added chemical synthesis and environmental remediation. However, their environmental applications lack of a comprehensive summary and in−depth discussion. In this review, recent progresses in synthesis routes and advanced characterization techniques for 2D SACs are introduced, and a comprehensive discussion on their applications in environmental remediation is presented. Generally, 2D SACs can be effective in catalytic elimination of aqueous and gaseous pollutants via radical or non−radical routes and transformation of toxic pollutants into less poisonous species or highly value−added products, opening a new horizon for the contaminant treatment. In addition, in−depth reaction mechanisms and potential pathways are systematically discussed, and the relationship between the structure−performance is highlighted. Finally, several critical challenges within this field are presented, and possible directions for further explorations of 2D SACs in environmental remediation are suggested. Although the research of 2D SACs in the environmental application is still in its infancy, this review will provide a timely summary on the emerging field, and would stimulate tremendous interest for designing more attractive 2D SACs and promoting their wide applications.

具有独特几何和电子结构的二维(2D)载体受限单原子催化剂(2D SAC)在不同的催化应用中具有吸引力,如能量转换和储存、增值化学合成和环境修复。然而,它们的环境应用缺乏全面的总结和深入的讨论。本文介绍了二维SAC的合成路线和先进表征技术的最新进展,并对其在环境修复中的应用进行了全面的讨论。通常,2D SAC可以通过自由基或非自由基途径有效地催化消除水性和气态污染物,并将有毒污染物转化为毒性较小的物种或高附加值的产品,为污染物处理开辟了新的领域。此外,系统地讨论了深度反应机制和潜在途径,并强调了结构-性能之间的关系。最后,提出了该领域的几个关键挑战,并提出了在环境修复中进一步探索2D SAC的可能方向。尽管2D SAC在环境应用中的研究仍处于起步阶段,但这篇综述将及时总结这一新兴领域,并将激发人们对设计更具吸引力的2D SAC并促进其广泛应用的极大兴趣。
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引用次数: 10
Towards the selectivity distinction of phenol hydrogenation on noble metal catalysts 贵金属催化剂上苯酚加氢选择性的区别
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-03-01 DOI: 10.1016/j.nanoms.2020.11.002
Shanjun Mao , Zhe Wang , Zhirong Chen , Kejun Wu , Kaichao Zhang , Qichuan Li , Huihuan Yan , Guofeng Lü , Guodong Huang , Yong Wang

Selective hydrogenation of phenol to cyclohexanone is intriguing in chemical industry. Though a few catalysts with promising performances have been developed in recent years, the basic principle for catalyst design is still missing owing to the unclear catalytic mechanism. This work tries to unravel the mechanism of phenol hydrogenation and the reasons causing the selectivity discrepancy on noble metal catalysts under mild conditions. Results show that different reaction pathways always firstly converge to the formation of cyclohexanone under mild conditions. The selectivity discrepancy mainly depends on the activity for cyclohexanone sequential hydrogenation, in which two factors are found to be responsible, i.e. the hydrogenation energy barrier and the competitive chemisorption between phenol and cyclohexanone, if the specific co-catalyzing effect of H2O on Ru is not considered. Based on the above results, a quantitative descriptor, Eb(one/pl)/Ea, in which Ea can be further correlated to the d band center of the noble metal catalyst, is proposed by the first time to roughly evaluate and predict the selectivity to cyclohexanone for catalyst screening.

苯酚选择性加氢制环己酮在化学工业中具有重要意义。尽管近年来开发了一些性能良好的催化剂,但由于催化机理尚不清楚,催化剂设计的基本原理仍然缺失。本工作试图揭示在温和条件下贵金属催化剂上苯酚加氢的机理以及导致选择性差异的原因。结果表明,在温和的条件下,不同的反应途径总是首先聚合形成环己酮。选择性差异主要取决于环己酮顺序加氢的活性,如果不考虑H2O对Ru的特定共催化作用,则发现两个因素是原因,即加氢能垒和苯酚与环己酮之间的竞争性化学吸附。基于上述结果,首次提出了一个定量描述符Eb(one/pl)/Ea,其中Ea可以与贵金属催化剂的d带中心进一步相关,以粗略评估和预测催化剂筛选对环己酮的选择性。
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引用次数: 5
Adjusting the interfacial adhesion via surface modification to prepare high-performance fibers 通过表面改性调节界面附着力制备高性能纤维
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-03-01 DOI: 10.1016/j.nanoms.2021.11.004
Ning Han , Xiaolin Zhao , Vijay Kumar Thakur

Ultra-high molecular weight polyethylene (UHMWPE) fiber is a new kind of high-performance fiber. Due to its excellent physical and chemical characteristics, it is widely used in various fields. However, the surface UHMWPE fiber is smooth and demonstrates no-polar groups. The weak interfacial adhesion between fiber and resin seriously restricts the applications of UHMWPE fiber. Therefore, the surface modification treatments of UHMWPE fiber are used to improve the interfacial adhesion strength. The modified method by adding nanomaterials elucidates the easy fabrication, advanced equipment and proper technology. Thus, the progress of UHMWPE nanocomposite fibers prepared via adding various nanofillers are reviewed. Meanwhile, the effects of other various methods on surface modification are also reviewed. This work advances the various design strategies about nano technologies on improving interfacial adhesion performance via treatment methodologies.

超高分子量聚乙烯(UHMWPE)纤维是一种新型的高性能纤维。由于其优异的物理和化学特性,它被广泛应用于各个领域。然而,表面UHMWPE纤维是光滑的,并且没有显示出极性基团。超高分子量聚乙烯纤维与树脂之间的界面附着力较弱,严重制约了其应用。因此,对UHMWPE纤维进行表面改性处理以提高界面粘合强度。添加纳米材料的改性方法说明了该方法制作简单、设备先进、工艺合理。综述了通过添加各种纳米填料制备超高分子量聚乙烯纳米复合纤维的研究进展。同时,还对其他各种方法在表面改性中的作用进行了综述。这项工作提出了关于纳米技术的各种设计策略,通过处理方法提高界面粘附性能。
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引用次数: 14
Additive manufacturing of Ni-based superalloys: Residual stress, mechanisms of crack formation and strategies for crack inhibition 镍基高温合金的增材制造:残余应力、裂纹形成机制和裂纹抑制策略
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-03-01 DOI: 10.1016/j.nanoms.2022.08.001
Chuan Guo , Gan Li , Sheng Li , Xiaogang Hu , Hongxing Lu , Xinggang Li , Zhen Xu , Yuhan Chen , Qingqing Li , Jian Lu , Qiang Zhu

The additive manufacturing (AM) of Ni-based superalloys has attracted extensive interest from both academia and industry due to its unique capabilities to fabricate complex and high-performance components for use in high-end industrial systems. However, the intense temperature gradient induced by the rapid heating and cooling processes of AM can generate high levels of residual stress and metastable chemical and structural states, inevitably leading to severe metallurgical defects in Ni-based superalloys. Cracks are the greatest threat to these materials’ integrity as they can rapidly propagate and thereby cause sudden and non-predictable failure. Consequently, there is a need for a deeper understanding of residual stress and cracking mechanisms in additively manufactured Ni-based superalloys and ways to potentially prevent cracking, as this knowledge will enable the wider application of these unique materials. To this end, this paper comprehensively reviews the residual stress and the various mechanisms of crack formation in Ni-based superalloys during AM. In addition, several common methods for inhibiting crack formation are presented to assist the research community to develop methods for the fabrication of crack-free additively manufactured components.

镍基高温合金的增材制造(AM)因其制造用于高端工业系统的复杂高性能部件的独特能力而吸引了学术界和工业界的广泛兴趣。然而,AM的快速加热和冷却过程引起的强烈温度梯度会产生高水平的残余应力和亚稳的化学和结构状态,不可避免地导致镍基高温合金出现严重的冶金缺陷。裂纹是对这些材料完整性的最大威胁,因为它们可以迅速传播,从而导致突然和不可预测的失效。因此,需要更深入地了解添加制造的镍基高温合金中的残余应力和开裂机制,以及潜在的防止开裂的方法,因为这些知识将使这些独特材料能够得到更广泛的应用。为此,本文全面回顾了镍基高温合金在AM过程中的残余应力和裂纹形成的各种机制。此外,还提出了几种抑制裂纹形成的常用方法,以帮助研究界开发无裂纹添加制造部件的制造方法。
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引用次数: 22
MXene-based electrochemical (bio) sensors for sustainable applications: Roadmap for future advanced materials 用于可持续应用的MXene电化学(生物)传感器:未来先进材料的路线图
IF 9.9 2区 材料科学 Q1 Engineering Pub Date : 2023-03-01 DOI: 10.1016/j.nanoms.2022.07.003
Qing Wang , Ning Han , Zhangfeng Shen , Xue Li , Zhijie Chen , Yue Cao , Weimeng Si , Fagang Wang , Bing-Jie Ni , Vijay Kumar Thakur

MXenes are emerging transition metal carbides and nitrides-based 2D conductive materials. They have found wide applications in sensors due to their excellent valuable properties. This paper reviews the recent research status of MXene-based electrochemical (bio) sensors for detecting biomarkers, pesticides, and other aspects. The first part of this paper introduced the synthesis strategy and the effect of surface modification on various properties of MXenes. The second part of this paper discussed the application of MXenes as electrode modifiers for detecting pesticides, environmental pollutants, and biomarkers such as glucose, hydrogen peroxide, etc. Hope this review will inspire more efforts toward research on MXene-based sensors to meet the growing requirements.

MXenes是新兴的过渡金属碳化物和氮化物基2D导电材料。由于其优异的有价值的特性,它们在传感器中得到了广泛的应用。本文综述了基于MXene的电化学(生物)传感器在检测生物标志物、农药等方面的研究现状。本文第一部分介绍了MXenes的合成策略以及表面改性对MXenes各种性能的影响。本文的第二部分讨论了MXenes作为电极改性剂在检测农药、环境污染物以及葡萄糖、过氧化氢等生物标志物方面的应用。希望这篇综述将激励人们更多地致力于基于MXenes的传感器的研究,以满足日益增长的需求。
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引用次数: 12
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