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Back Cover Image, Volume 6, Number 11, November 2024
IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-11-27 DOI: 10.1002/cey2.705
Takashi Hakari, Yuto Kameoka, Kaihei Kishida, Shinji Ozaki, Chihiro Murata, Minako Deguchi, Ryo Harada, Tomoki Fujisawa, Yusuke Mizuno, Heisuke Nishikawa, Tomoyuki Tamura, Yiqun Wang, Hikari Takahara, Takashi Aoki, Tokuo Inamasu, Daisuke Okuda, Masashi Ishikawa

Back cover image: A lightweight battery has been successfully created using a cathode that uses sulfur, which is abundant as a resource, as the active material. The battery uses an electrolyte solution and is lightweight, with the goal of becoming a power source for next-generation aircraft. The graphic depicts the mining of abundant sulfur, which is then delivered to a large battery center by a series of transportation systems. It also symbolically shows that the battery that takes off from that battery center powers the aircraft. The fact that both the batteries on the ground and in the air have an liquid electrolyte is shown in translucent form. Furthermore, the present graphic implies that the electricity stored in the batteries is generated by hydroelectric power, a renewable energy source, and together with the green ground, giving the impression of the total system that is environmentally friendly.

Article number: 10.1002/cey2.585

Takashi Hakari & Masashi Ishikawa

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引用次数: 0
Cover Image, Volume 6, Number 11, November 2024
IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-11-27 DOI: 10.1002/cey2.704
Zhijian Du, La Li, Guozhen Shen

Front cover image: Proton-conducting hydrogel is one of the most attractive candidates as an electrolyte for assembling into a thermally chargeable supercapacitor (TCSC). In article cey2.562, Shen et al. proposed a high performance thermoelectric and photo-thermoelectric dual-output TCSC by attaching binder-free Ti3C2Tx MXene@PPy electrodes to both ends of a terpolymer proton-conducting hydrogel. The real-time human movement and health monitoring of the strain sensor powered by assembled TCSC devices are successfully realized.

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引用次数: 0
Back Cover Image, Volume 6, Number 10, October 2024 封底图片,第 6 卷第 10 号,2024 年 10 月
IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-10-25 DOI: 10.1002/cey2.688
Qihang Ding, Zewen Jiang, Kean Chen, Hui Li, Jingzhe Shi, Xinping Ai, Dingguo Xia

Back cover image: High-voltage LiCoO2 can deliver a high capacity and therefore significantly boost the energy density of Li-ion batteries. However, its poor cyclability is still an issue for commercial applications. In article number CEY2-2024-0118, Ding et al. proposed a facile but effective methode to address this issue by constructing a LiF modification layer on LiCoO2 surface via pyrolysis of the lithiated polyvinylidene fluoride pre-coating under air atmosphere. The as-fabricated LiF layer can effectively suppress the interfacial side reactions and surface structure degradation, and thereby greatly enhance the cycling stability of LiCoO2 cathode at high charge cutoff voltage of 4.6 V.

封底图片:高压钴酸锂可提供高容量,从而显著提高锂离子电池的能量密度。然而,其循环性差仍然是商业应用中的一个问题。在编号为 CEY2-2024-0118 的文章中,Ding 等人提出了一种简便而有效的方法来解决这一问题,即在空气环境下通过热解锂化聚偏氟乙烯预涂层在钴酸锂表面构建锂氟改性层。所制备的锂化物改性层可有效抑制界面副反应和表面结构退化,从而大大提高钴酸锂阴极在 4.6 V 高电荷截止电压下的循环稳定性。
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引用次数: 0
Cover Image, Volume 6, Number 10, October 2024 封面图片,第 6 卷第 10 号,2024 年 10 月
IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-10-25 DOI: 10.1002/cey2.687
Li-Feng Zhou, Jia-Yang Li, Jian Peng, Li-Ying Liu, Hang Zhang, Yi-Song Wang, Yameng Fan, Jia-Zhao Wang, Tao Du

Front cover image: Phosphate cathodes in aqueous zinc-based batteries have garnered significant research interest for large-scale green energy storage. However, unclear mechanisms are hindering the progress of their research and application. In article number CEY2-2024-0147, various categories of phosphate materials used as zinc-based battery cathodes are summarized. The article discusses current advances and critical perspectives, aiming to elucidate the structural and chemical information related to Zn2+ storage mechanisms in phosphate cathodes using advanced characterization techniques.

封面图片:锌基水性电池中的磷酸盐阴极在大规模绿色能源储存方面引起了人们的极大研究兴趣。然而,机制不清阻碍了其研究和应用的进展。在文章编号 CEY2-2024-0147 中,总结了用作锌基电池阴极的各类磷酸盐材料。文章讨论了当前的研究进展和重要观点,旨在利用先进的表征技术阐明磷酸盐阴极中与 Zn2+ 储存机制相关的结构和化学信息。
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引用次数: 0
Interface and doping engineering of V2C-MXene-based electrocatalysts for enhanced electrocatalysis of overall water splitting 基于 V2C-MXene 的电催化剂的界面和掺杂工程,以增强整体水分离的电催化性能
IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-10-23 DOI: 10.1002/cey2.583
Yousen Wu, Jinlong Li, Guozhe Sui, Dong-Feng Chai, Yue Li, Dongxuan Guo, Dawei Chu, Kun Liang

The restacking and oxidizable nature of vanadium-based carbon/nitride (V2C-MXene) poses a significant challenge. Herein, tellurium (Te)-doped V2C/V2O3 electrocatalyst is constructed via mild H2O2 oxidation and calcination treatments. Especially, this work rationally exploits the inherent easy oxidation characteristic associated with MXene to alter the interfacial information, thereby obtaining stable self-generated vanadium-based heterointerfaces. Meanwhile, the microetching effect of H2O2 creates numerous pores to address the restacking issues. Besides, Te element doping settles the issue of awkward levels of absorption/desorption ability of intermediates. The electrocatalyst obtains an unparalleled hydrogen evolution reaction and oxygen evolution reaction with the overpotential of 83.5 and 279.8 mV at −10 and 10 mA cm−2, respectively. In addition, the overall water-splitting device demonstrates a low cell voltage of 1.41 V to obtain 10 mA cm−2. Overall, the inherent drawbacks of MXene can be turned into benefits based on the planning strategy to create these electrocatalysts with desirable reaction kinetics.

钒基碳/氮化物(V2C-MXene)的重堆叠和可氧化特性是一项重大挑战。本文通过温和的 H2O2 氧化和煅烧处理,构建了掺杂碲(Te)的 V2C/V2O3 电催化剂。特别是,这项工作合理地利用了 MXene 固有的易氧化特性来改变界面信息,从而获得了稳定的自生成钒基异质界面。同时,H2O2 的微蚀效应产生了大量孔隙,从而解决了重新堆叠问题。此外,Te 元素的掺杂解决了中间体吸收/解吸能力水平尴尬的问题。该电催化剂在-10 和 10 mA cm-2 的过电位分别为 83.5 和 279.8 mV,从而获得了无与伦比的氢进化反应和氧进化反应。此外,整个分水装置的电池电压低至 1.41 V,即可获得 10 mA cm-2。总之,根据规划策略,可以将 MXene 的固有缺点转化为具有理想反应动力学的电催化剂的优点。
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引用次数: 0
Back Cover Image, Volume 6, Number 9, September 2024 封底图片,第 6 卷第 9 号,2024 年 9 月
IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-09-30 DOI: 10.1002/cey2.660
Qi Lai, Bincen Yin, Yu Dou, Qing Zhang, Yunhai Zhu, Yingkui Yang

Back cover image: To achieve high-performance practical batteries, synergistically engineering intrinsic defects and heterostructures of metal oxide electrodes is highly desirable but remains challenging. In article number cey2.517, Yang et al. report on the crafting of hierarchically-electrospun carbon nanofibers integrated with oxygen vacancies-enriched V2O3 nanosheets. Accordingly, the as-fabricated V2O3 anode shows high reversible capacity, superior rate capability, and long cycling stability. An all-electrospun full-battery with an electrospun V2O5 cathode and an electrospun polyimide separator is further assembled that delivers an impressive energy density at the high power density.

封底图片:要实现高性能的实用电池,对金属氧化物电极的固有缺陷和异质结构进行协同工程设计是非常理想的,但仍然具有挑战性。在编号为 cey2.517 的文章中,Yang 等人报告了分层电纺碳纳米纤维与富含氧空位的 V2O3 纳米片的制作工艺。因此,制造出的 V2O3 阳极显示出高可逆容量、卓越的速率能力和长循环稳定性。通过电纺 V2O5 阴极和电纺聚酰亚胺隔膜,进一步组装出全电纺全电池,可在高功率密度下提供惊人的能量密度。
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引用次数: 0
Cover Image, Volume 6, Number 9, September 2024 封面图片,第 6 卷第 9 号,2024 年 9 月
IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-09-30 DOI: 10.1002/cey2.659
Vaiyapuri Soundharrajan, Sungjin Kim, Subramanian Nithiananth, Muhammad H. Alfaruqi, JunJi Piao, Duong Tung Pham, Vinod Mathew, Sang A. Han, Jung Ho Kim, Jaekook Kim

Front cover image: The cover picture shows the selection and theoretical validation of transition metal ions for constructing a new class of cathode material, Na3VFe0.5Ti0.5(PO4)3/C, with NASICON-type structure for SIBs. The combination of V, Fe and Ti elements allows Na+ ions to mobile without stress in the cathode, which results in stable electrochemical characteristics. In article number https://doi.org/10.1002/cey2.551, Soundharrajan et al.

封面图片:封面图片显示了对过渡金属离子的选择和理论验证,以构建具有 NASICON 型结构的新型 SIB 阴极材料 Na3VFe0.5Ti0.5(PO4)3/C。V、Fe 和 Ti 元素的结合使 Na+ 离子在阴极中无应力移动,从而产生稳定的电化学特性。在第 https://doi.org/10.1002/cey2.551 号文章中,Soundharrajan 等人提出了一种新的 SIB。
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引用次数: 0
Sustainable nitrogen photofixation: Considerations on the state of the art of non critical carbon materials 可持续的氮光固化:对非关键碳材料最新技术的思考
IF 20.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-09-19 DOI: 10.1002/cey2.545
Federica Valentini, Amalia M. Grigoras, Luigi Vaccaro, Loredana Latterini
The achievement of a carbon-neutral energy economy is nowadays mandatory to face global warming and the current energy crisis. To mitigate the present and future environmental issues, replacing fossil feedstocks with renewable sources is of primary importance, aiming to meet future generations' demands for energy and commodities. In light of this, the revamp of the ammonia synthesis, which today consumes almost 2% of the energy globally produced, gained increasing interest. The ammonia generation by reacting air and water and using sunlight as an inexhaustible source of energy is the closest approach to the ideal situation for zero-carbon energy and chemical production. To promote solar-to-ammonia production, the photocatalyst plays a crucial role. However, for large-scale implementation and long-term utilization, the selection of noncritical raw materials in catalyst preparation is central aiming at resource security. In this context, herein are reviewed different strategies developed to improve the photocatalytic performances of carbon-based materials. The introduction of vacancies and surface doping are discussed as valuable approaches to enhance the photocatalytic activity in the nitrogen fixation reactions, as well as the construction of heterojunctions to finely tune the electronic properties of carbon-based materials.
为了应对全球变暖和当前的能源危机,实现碳中和能源经济已成为当务之急。为了缓解当前和未来的环境问题,用可再生能源替代化石原料至关重要,其目的是满足后代对能源和商品的需求。有鉴于此,对氨合成的改造日益受到关注,目前,氨合成消耗的能源几乎占全球生产能源的 2%。通过空气和水的反应生成氨,并利用太阳光这一取之不尽的能源,是最接近零碳能源和化学品生产理想状态的方法。要促进太阳能制氨,光催化剂起着至关重要的作用。然而,为了大规模实施和长期利用,在催化剂制备过程中选择非关键原材料是确保资源安全的关键。在此背景下,本文回顾了为改善碳基材料的光催化性能而开发的不同策略。其中讨论了引入空位和表面掺杂作为提高固氮反应中光催化活性的重要方法,以及构建异质结以微调碳基材料的电子特性。
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引用次数: 0
Composite electrolytes and interface designs for progressive solid-state sodium batteries 用于渐进式固态钠电池的复合电解质和界面设计
IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-09-12 DOI: 10.1002/cey2.628
Junyu Hou, Tianke Zhu, Gang Wang, Rongrong Cheacharoen, Wu Sun, Xingyu Lei, Qunyao Yuan, Dalin Sun, Jie Zhao

Solid-state sodium batteries (SSSBs) are poised to replace lithium-ion batteries as viable alternatives for energy storage systems owing to their high safety and reliability, abundance of raw material, and low costs. However, as the core constituent of SSSBs, solid-state electrolytes (SSEs) with low ionic conductivities at room temperature (RT) and unstable interfaces with electrodes hinder the development of SSSBs. Recently, composite SSEs (CSSEs), which inherit the desirable properties of two phases, high RT ionic conductivity, and high interfacial stability, have emerged as viable alternatives; however, their governing mechanism remains unclear. In this review, we summarize the recent research progress of CSSEs, classified into inorganic–inorganic, polymer–polymer, and inorganic–polymer types, and discuss their structure–property relationship in detail. Moreover, the CSSE–electrode interface issues and effective strategies to promote intimate and stable interfaces are summarized. Finally, the trends in the design of CSSEs and CSSE–electrode interfaces are presented, along with the future development prospects of high-performance SSSBs.

固态钠电池(SSSB)具有安全性高、可靠性强、原材料丰富、成本低廉等优点,有望取代锂离子电池,成为储能系统的可行替代品。然而,作为 SSSB 的核心成分,固态电解质(SSE)在室温(RT)下的离子电导率较低,且与电极的界面不稳定,这阻碍了 SSSB 的发展。最近,复合固态电解质(CSSEs)作为一种可行的替代品出现了,它继承了两相、高室温离子电导率和高界面稳定性等理想特性;然而,它们的作用机制仍不清楚。在这篇综述中,我们总结了 CSSE 的最新研究进展,将其分为无机-无机型、聚合物-聚合物型和无机-聚合物型,并详细讨论了它们的结构-性能关系。此外,还总结了 CSSE-电极界面问题以及促进亲密稳定界面的有效策略。最后,介绍了 CSSE 和 CSSE-电极界面设计的发展趋势,以及高性能 SSSB 的未来发展前景。
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引用次数: 0
Two-dimensional carbonitride MXenes: From synthesis to properties and applications 二维碳氮化物 MXenes:从合成到特性和应用
IF 20.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-09-12 DOI: 10.1002/cey2.609
Weiwei Zhang, Shibo Li, Xiachen Fan, Xuejin Zhang, Shukai Fan, Guoping Bei
Carbonitride MXenes, such as Ti3CNTx, Ti2C0.5N0.5Tx, and Ti4(C0.2N0.8)3Tx, have attracted much interest in the large family of two-dimensional (2D) nanomaterials. Like their carbide MXene counterparts, the nanolayered structure and functional groups endow carbonitride MXenes with an attractive combination of physical and chemical properties. More interestingly, the replacement of C by N changes the lattice parameters and electron distribution of carbonitride MXenes due to the greater electronegativity of N as compared to C, thus resulting in significantly enhanced functional properties. This paper reviews the development of carbonitride MXenes, the preparation of 2D carbonitride MXenes, and the current understanding of the microstructure, electronic structure, and functional properties of carbonitride MXenes. In addition, applications, especially in energy storage, sensors, catalysts, electromagnetic wave shielding and absorption, fillers, and environmental and biomedical fields, are summarized. Finally, their current limitations and future opportunities are presented.
碳化物 MXenes(如 Ti3CNTx、Ti2C0.5N0.5Tx 和 Ti4(C0.2N0.8)3Tx)在庞大的二维(2D)纳米材料家族中备受关注。与碳化物 MXene 相似,纳米层状结构和官能团赋予了碳氮化物 MXene 极具吸引力的物理和化学特性组合。更有趣的是,由于 N 的电负性比 C 大,用 N 替代 C 会改变碳氮化物 MXenes 的晶格参数和电子分布,从而显著增强其功能特性。本文回顾了碳氮化物 MXenes 的发展、二维碳氮化物 MXenes 的制备以及目前对碳氮化物 MXenes 的微观结构、电子结构和功能特性的理解。此外,还概述了其应用,特别是在能量存储、传感器、催化剂、电磁波屏蔽和吸收、填料以及环境和生物医学领域的应用。最后,介绍了它们目前的局限性和未来的机遇。
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引用次数: 0
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Carbon Energy
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