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Ultrahigh-ratio drawing during spinning achieves graphene fibres with high strength and thermal conductivity 纺丝时的超高拉伸率使石墨烯纤维具有高强度和高导热性。
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-28 DOI: 10.1038/s41563-026-02733-0
Senping Liu, Jinhe Wang, Yiwei Zhang, Bo Wang, Min Cao, Jiahao Lu, Jinxu Lin, Ya Wang, Yingjun Liu, Dan Chang, Peng Li, Dingyi Pan, Chao Gao, Zhen Xu
{"title":"Ultrahigh-ratio drawing during spinning achieves graphene fibres with high strength and thermal conductivity","authors":"Senping Liu, Jinhe Wang, Yiwei Zhang, Bo Wang, Min Cao, Jiahao Lu, Jinxu Lin, Ya Wang, Yingjun Liu, Dan Chang, Peng Li, Dingyi Pan, Chao Gao, Zhen Xu","doi":"10.1038/s41563-026-02733-0","DOIUrl":"10.1038/s41563-026-02733-0","url":null,"abstract":"The demand for materials combining high strength with exceptional thermal conductivity is growing across aerospace, automotive, thermal management and energy applications. Graphene offers an ideal building block, but multiscale defects such as disordered stacking and voids prevent macroscopic assemblies from realizing its intrinsic properties. Here we show that ultrahigh-ratio draw spinning, enabled by the polymer-like viscoelasticity of two-dimensional sheets in viscous solvents, produces graphene fibres with a tensile strength of 5.9 GPa, a Young modulus of 963 GPa, a thermal conductivity of up to 1,720 W m−1 K−1 and an electrical conductivity of 1.3 MS m−1. A high-ratio draw spinning up to 11, combined with high-temperature annealing, efficiently removes defects and produces densely packed, highly ordered graphene fibres. These properties surpass most existing strong and thermally conductive fibres. This work provides a versatile route for assembling two-dimensional materials into high-performance macroscopic structures and expands opportunities for multifunctional materials. Polymer-like viscoelasticity of two-dimensional graphene oxide in viscous solvents enables ultrahigh-ratio drawing during fibre spinning, which achieves macroscopic graphene fibres with a compelling combination of high mechanical strength, thermal conductivity and electrical conductivity.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"25 10","pages":"1732-1740"},"PeriodicalIF":38.0,"publicationDate":"2026-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148851156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Controlling ferroelectric-like gating in two‑dimensional stacks 在二维堆叠中控制类铁电门控。
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-27 DOI: 10.1038/s41563-026-02719-y
Xiangyan Han, Jianming Lu
{"title":"Controlling ferroelectric-like gating in two‑dimensional stacks","authors":"Xiangyan Han, Jianming Lu","doi":"10.1038/s41563-026-02719-y","DOIUrl":"10.1038/s41563-026-02719-y","url":null,"abstract":"Graphene encapsulated in hexagonal boron nitride sometimes shows a puzzling ferroelectric-like memory effect. A rotatable device reveals that this effect can be turned on and off by twisting the two hexagonal boron nitride layers away from perfect alignment, resolving debates and raising fundamental questions about the microscopic origin of interface polarity in twisted van der Waals stacks.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"25 10","pages":"1676-1677"},"PeriodicalIF":38.0,"publicationDate":"2026-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148840784","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Magneto-optics marches on 磁光学继续前进
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-26 DOI: 10.1038/s41563-026-02743-y
{"title":"Magneto-optics marches on","authors":"","doi":"10.1038/s41563-026-02743-y","DOIUrl":"10.1038/s41563-026-02743-y","url":null,"abstract":"Continued developments in materials synthesis and light sources are driving the discovery of magneto-optical phenomena.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"25 9","pages":"1473-1473"},"PeriodicalIF":38.0,"publicationDate":"2026-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.comhttps://www.nature.com/articles/s41563-026-02743-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148816688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Void suppressive lithium anodes for all-solid-state batteries. 全固态电池用抑制空隙的锂阳极。
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-26 DOI: 10.1038/s41563-026-02729-w
Xiao Ji, Yijie Liu, Xinzi He, Singyuk Hou, Jijian Xu, Kimberly S Reeves, Michael J Zachman, Ji Chen, Tao Deng, Jiaxun Zhang, Miaofang Chi, Chunsheng Wang
{"title":"Void suppressive lithium anodes for all-solid-state batteries.","authors":"Xiao Ji, Yijie Liu, Xinzi He, Singyuk Hou, Jijian Xu, Kimberly S Reeves, Michael J Zachman, Ji Chen, Tao Deng, Jiaxun Zhang, Miaofang Chi, Chunsheng Wang","doi":"10.1038/s41563-026-02729-w","DOIUrl":"10.1038/s41563-026-02729-w","url":null,"abstract":"<p><p>The all-solid-state lithium metal battery is a promising next-generation energy-storage technology due to it offering high energy density and safety. However, the issues of void formation and dendrite growth both remain unsolved. Here we demonstrate that void formation is controlled by the product of lithium full stripping areal capacity and applied current density, which we define as the void suppression capability (VSC). The VSC is enhanced by increasing self-diffusivity and initial lithium atom concentration. Using a Mg-1 wt% La inoculant in molten lithium (LiMgLa) to refine grains, lithium self-diffusivity and VSC are enhanced, resulting in an increase in the critical current density/capacity from 1.2 mA cm<sup>-2</sup>/0.6 mAh cm<sup>-2</sup> for the LiMg anode to 2.2 mA cm<sup>-2</sup>/1.1 mAh cm<sup>-2</sup> for the LiMgLa anode. The LiMgLa anodes enable stable lithium plating/stripping for over 1,200 h at 0.7 mA cm<sup>-2</sup> at room temperature. Phase-field modelling shows that the interfacial overpotential will be higher than the critical overpotential of the electrolyte when the stripped capacity is larger than 70% of the full depletion capacity, leading to dendrite growth and cell failure. Our observations offer a route to the design of all-solid-state lithium metal batteries with high powers and energy densities.</p>","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":" ","pages":""},"PeriodicalIF":38.0,"publicationDate":"2026-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148830886","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Triggering conversion in vanadium electrodes 钒电极的触发转换
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-26 DOI: 10.1038/s41563-026-02714-3
Stefan A. Freunberger
{"title":"Triggering conversion in vanadium electrodes","authors":"Stefan A. Freunberger","doi":"10.1038/s41563-026-02714-3","DOIUrl":"10.1038/s41563-026-02714-3","url":null,"abstract":"Using transition metals efficiently in aqueous batteries requires transferring multiple electrons per metal, which leads to difficult-to-manage conversion reactions. It is now shown how vanadium can be changed from one-electron insertion to four-electron conversion.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"25 9","pages":"1482-1483"},"PeriodicalIF":38.0,"publicationDate":"2026-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148816685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Crystal nucleation and growth in high-entropy alloys revealed by atomic electron tomography. 原子电子层析成像研究高熵合金的晶体成核和生长。
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-25 DOI: 10.1038/s41563-026-02727-y
Yakun Yuan, Saman Moniri, Yao Yang, Jihan Zhou, Andrew Yuan, Dennis S Kim, Yongsoo Yang, Chenyang Li, Kun Luo, Qi An, Wei Chen, Peter Ercius, Jianwei Miao
{"title":"Crystal nucleation and growth in high-entropy alloys revealed by atomic electron tomography.","authors":"Yakun Yuan, Saman Moniri, Yao Yang, Jihan Zhou, Andrew Yuan, Dennis S Kim, Yongsoo Yang, Chenyang Li, Kun Luo, Qi An, Wei Chen, Peter Ercius, Jianwei Miao","doi":"10.1038/s41563-026-02727-y","DOIUrl":"https://doi.org/10.1038/s41563-026-02727-y","url":null,"abstract":"<p><p>High-entropy alloys combine multiple principal elements and can exhibit exceptional mechanical properties and catalytic activity. However, how they crystallize remains poorly understood because early nuclei are small, transient and chemically complex. Here we advance atomic electron tomography to determine the three-dimensional atomic structures and local chemical order of 8,160 high- and medium-entropy alloy nuclei. We find that nucleation proceeds through gradient ordering, in which structural order is highest at the core, decreases smoothly towards the boundary and is coupled to local chemical order. Most nuclei coalesce with nearly aligned crystal lattices, whereas a minority form twin boundaries. We develop the gradient nucleation pathways model, which generalizes classical nucleation theory by incorporating spatially varying structural order within each nucleus. The model captures diffuse, partially ordered nuclei, recovers classical nucleation theory in the sharp-interface limit and reveals multiple intermediate states. These results provide an atomistic framework for understanding crystal nucleation and growth across a broad range of materials.</p>","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":" ","pages":""},"PeriodicalIF":38.0,"publicationDate":"2026-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148818921","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Electrical manipulation and detection of perpendicular altermagnetic order via a proximitized Dirac semimetal. 通过近似狄拉克半金属的电操作和垂直交变顺序的检测。
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-24 DOI: 10.1038/s41563-026-02721-4
Zhaohui Li, Wenqing He, Hua Bai, Yang Wang, Alexander J Grutter, Guoyi Shi, Xiwen Zhang, Christy Kinane, Andrew Caruana, Hui Ru Tan, Yuchen Pu, Chenhui Zhang, Yongxi Wang, Hanbum Park, Anjan Soumyanarayanan, Lei Shen, Hyunsoo Yang
{"title":"Electrical manipulation and detection of perpendicular altermagnetic order via a proximitized Dirac semimetal.","authors":"Zhaohui Li, Wenqing He, Hua Bai, Yang Wang, Alexander J Grutter, Guoyi Shi, Xiwen Zhang, Christy Kinane, Andrew Caruana, Hui Ru Tan, Yuchen Pu, Chenhui Zhang, Yongxi Wang, Hanbum Park, Anjan Soumyanarayanan, Lei Shen, Hyunsoo Yang","doi":"10.1038/s41563-026-02721-4","DOIUrl":"10.1038/s41563-026-02721-4","url":null,"abstract":"<p><p>Altermagnets, which combine antiferromagnetic-like magnetic compensation with ferromagnetic-like broken time-reversal symmetry, hold great promise for high-density and ultrafast spintronic applications. However, the detection and switching of perpendicular altermagnetic order are fundamentally constrained by magnetic symmetry, restricting both fundamental studies and practical implementation. Here we demonstrate the robust electrical reading and deterministic switching of perpendicular altermagnetic order by designing a Dirac semimetal/altermagnet heterostructure of PtTe<sub>2</sub>/CrSb. This engineered interface enables anomalous Hall read-out via the altermagnetic proximity effect and delivers efficient spin-orbit torque for manipulating the epitaxial perpendicular Néel vector in CrSb. These findings substantially broaden the functional scope of altermagnetic heterostructures and pave the way for scalable altermagnetic memory.</p>","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":" ","pages":""},"PeriodicalIF":38.0,"publicationDate":"2026-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148813631","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Flux-mediated ligand exchange restructures metal-organic framework glasses. 通量介导的配体交换重组金属-有机框架玻璃。
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-24 DOI: 10.1038/s41563-026-02712-5
Jan-Benedikt Weiß, Lorena Fritsch, Michele Tricarico, Anke Schoch, Soma Salamon, Wen-Long Xue, Chinmoy Das, Pascal Kolodzeiski, Heiko Wende, Jin-Chong Tan, Matthias Bauer, Sebastian Henke
{"title":"Flux-mediated ligand exchange restructures metal-organic framework glasses.","authors":"Jan-Benedikt Weiß, Lorena Fritsch, Michele Tricarico, Anke Schoch, Soma Salamon, Wen-Long Xue, Chinmoy Das, Pascal Kolodzeiski, Heiko Wende, Jin-Chong Tan, Matthias Bauer, Sebastian Henke","doi":"10.1038/s41563-026-02712-5","DOIUrl":"10.1038/s41563-026-02712-5","url":null,"abstract":"<p><p>Melt-quenched glasses derived from metal-organic frameworks (MOFs) combine the processability of glasses with the modularity and microporosity of MOFs, yet remain structurally and functionally less diverse than crystalline analogues. Here we show that the chelating ligand 1,10-phenanthroline acts as an organic flux that lowers the glass transition temperature of selected MOFs and induces ligand exchange during melting, thereby enabling control over local coordination and global topology in MOF glasses. In Co<sup>2+</sup>-based systems, phenanthroline coordinates to the metal nodes, increases the coordination number and reduces network connectivity by forming terminal ligands. This coordination sphere engineering affords a level of structural control not readily achievable in conventional inorganic or organic glasses. Crucially, the lower processing temperature suppresses thermal decomposition, enabling the synthesis of Co<sup>2+</sup>-based MOF glasses free of magnetic impurities. These glasses exhibit antiferromagnetic coupling and represent unique examples of magnetic MOF glasses formed by melt quenching. Finally, we extend the strategy to otherwise non-meltable carboxylate-based MOFs, establishing flux-mediated ligand exchange as a versatile route to hybrid glasses with tailored connectivity and properties.</p>","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":" ","pages":""},"PeriodicalIF":38.0,"publicationDate":"2026-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148813657","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
From equilibrium to ultrafast antiferromagnetism 从平衡到超快反铁磁性。
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-19 DOI: 10.1038/s41563-026-02686-4
Alexey V. Kimel, Boris A. Ivanov, Dmytro Afanasiev
{"title":"From equilibrium to ultrafast antiferromagnetism","authors":"Alexey V. Kimel,&nbsp;Boris A. Ivanov,&nbsp;Dmytro Afanasiev","doi":"10.1038/s41563-026-02686-4","DOIUrl":"10.1038/s41563-026-02686-4","url":null,"abstract":"Although ferromagnets are known from ancient times, antiferromagnets were only discovered in the twentieth century and represent a much larger, less explored class of magnets. In this Review, we present the current understanding of the ultrafast response of spins in antiferromagnets to ultrashort laser stimuli. We progressively transition from equilibrium to ultrafast out-of-equilibrium dynamics, highlighting fundamental pillars that make the ultrafast magnetic response in antiferromagnets qualitatively distinct, compared with that in ferromagnets. Throughout this Review, we demonstrate how ultrashort laser excitation serves as a powerful tool for investigating and controlling antiferromagnets, providing access to coherent terahertz spin dynamics, dissipation mechanisms, nonlinear interactions and magnetic switching on ultrafast timescales. This unique combination of rich fundamental physics and advanced control capabilities positions antiferromagnets as both a fascinating subject of basic research and a promising platform for next-generation ultrafast and low-dissipation spintronic technologies. This Review presents a symmetry-based classification of antiferromagnetism and discusses the progress and challenges in detecting, exciting and probing the dynamics of antiferromagnets.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"25 9","pages":"1519-1532"},"PeriodicalIF":38.0,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148795932","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Reticular chemistry mimics enzyme pockets 网状化学模拟酶袋。
IF 38 1区 材料科学
Nature Materials Pub Date : 2026-08-19 DOI: 10.1038/s41563-026-02716-1
Himan Dev Singh, Wendy L. Queen
{"title":"Reticular chemistry mimics enzyme pockets","authors":"Himan Dev Singh,&nbsp;Wendy L. Queen","doi":"10.1038/s41563-026-02716-1","DOIUrl":"10.1038/s41563-026-02716-1","url":null,"abstract":"Two metal–organic frameworks, built from the same node and differing only in the twist of their tritopic linker, reorient metal sites while leaving chemistry, porosity and topology unchanged, showing that confinement can be programmed by design: the more confined framework captures nearly four times as much CO2 from air.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"25 10","pages":"1678-1679"},"PeriodicalIF":38.0,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148795880","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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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