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Moiré turns neuromorphic 摩尔纹变成神经形态
IF 37.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-30 DOI: 10.1038/s41563-024-01977-y
Wei Fan
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引用次数: 0
Quantifying the atomic neighbourhoods in complex concentrated alloys 量化复杂浓缩合金中的原子邻域
IF 37.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-30 DOI: 10.1038/s41563-024-01959-0
Arun Devaraj
Atom probe tomography unlocks the potential to precisely analyse the short-range ordering in a CoCrNi medium-entropy alloy.
原子探针层析技术为精确分析钴铬镍中熵合金中的短程有序释放了潜力。
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引用次数: 0
Moiré beyond van der Waals 超越范德瓦耳斯的摩尔纹
IF 37.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-30 DOI: 10.1038/s41563-024-01999-6
Inspired by non-trivial band topology and the variety of correlated electronic phases in moiré superlattices formed in van der Waals materials, scientists are finding alternative material platforms to exploit the rich phenomena arising from the twist-angle degree of freedom.
受范德华材料中形成的非三维带拓扑和摩尔纹超格中各种相关电子相的启发,科学家们正在寻找替代材料平台,以利用扭角自由度产生的丰富现象。
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引用次数: 0
Let’s twist again 让我们再扭一扭
IF 37.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-30 DOI: 10.1038/s41563-024-01969-y
Grace A. R. Rohaley, Torsten Hegmann
Filamentous viruses are a tunable platform for understanding the propagation of chirality across length scales, starting from the helical organization of major coat proteins on the virion surface to the liquid crystalline cholesteric phases formed in aqueous suspensions.
从病毒表面主要衣壳蛋白的螺旋组织到水悬浮液中形成的液晶胆甾相,丝状病毒是了解胆甾相跨长度尺度传播的一个可调平台。
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引用次数: 0
Cation-eutaxy-enabled III–V-derived van der Waals crystals as memristive semiconductors 作为记忆半导体的阳离子外延型 III-V 范德华晶体
IF 37.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-28 DOI: 10.1038/s41563-024-01986-x
Jihong Bae, Jongbum Won, Taeyoung Kim, Sangjin Choi, Hyesoo Kim, Seung-Hyun Victor Oh, Giyeok Lee, Eunsil Lee, Sijin Jeon, Minjung Kim, Hyung Wan Do, Dongchul Seo, Sungsoon Kim, Youngjun Cho, Hyeonsoo Kang, Bokyeong Kim, Hong Choi, Jihoon Han, Taehoon Kim, Narguess Nemati, Chanho Park, Kyuho Lee, Hongjae Moon, Jeongmin Kim, Hyunggeun Lee, Daniel W. Davies, Dohyun Kim, Seunghun Kang, Byung-Kyu Yu, Jaegyeom Kim, Min Kyung Cho, Jee-Hwan Bae, Soohyung Park, Jungkil Kim, Ha-Jun Sung, Myung-Chul Jung, In Chung, Heonjin Choi, Hyunyong Choi, Dohun Kim, Hionsuck Baik, Jae-Hyun Lee, Heejun Yang, Yunseok Kim, Hong-Gyu Park, Wooyoung Lee, Kee Joo Chang, Miso Kim, Dong Won Chun, Myung Joon Han, Aron Walsh, Aloysius Soon, Jinwoo Cheon, Cheolmin Park, Jong-Young Kim, Wooyoung Shim
Novel two-dimensional semiconductor crystals can exhibit diverse physical properties beyond their inherent semiconducting attributes, making their pursuit paramount. Memristive properties, as exemplars of these attributes, are predominantly manifested in wide-bandgap materials. However, simultaneously harnessing semiconductor properties alongside memristive characteristics to produce memtransistors is challenging. Herein we prepared a class of semiconducting III–V-derived van der Waals crystals, specifically the HxA1–xBX form, exhibiting memristive characteristics. To identify candidates for the material synthesis, we conducted a systematic high-throughput screening, leading us to 44 prospective III–V candidates; of these, we successfully synthesized ten, including nitrides, phosphides, arsenides and antimonides. These materials exhibited intriguing characteristics such as electrochemical polarization and memristive phenomena while retaining their semiconductive attributes. We demonstrated the gate-tunable synaptic and logic functions within single-gate memtransistors, capitalizing on the synergistic interplay between the semiconducting and memristive properties of our two-dimensional crystals. Our approach guides the discovery of van der Waals materials with unique properties from unconventional crystal symmetries. New two-dimensional semiconductors may exhibit properties beyond inherent semiconducting attributes. Here the authors report protonated semiconducting III–V-derived van der Waals crystals with memristive properties.
新型二维半导体晶体除了其固有的半导体特性外,还能表现出多种物理特性,因此对它们的研究至关重要。作为这些特性的典范,记忆特性主要体现在宽带隙材料中。然而,同时利用半导体特性和忆阻性特性来生产忆阻器是一项挑战。在此,我们制备了一类半导体 III-V 衍生范德华晶体,特别是 HxA1-xBX 形式,表现出记忆特性。为了确定材料合成的候选材料,我们进行了系统的高通量筛选,最终确定了 44 种 III-V 候选材料,并成功合成了其中的 10 种,包括氮化物、磷化物、砷化物和锑化物。这些材料在保留其半导体特性的同时,还表现出了电化学极化和忆阻现象等引人入胜的特性。我们利用二维晶体的半导体特性和记忆特性之间的协同作用,在单门记忆晶体管中展示了门调节突触和逻辑功能。我们的研究方法指导着人们从非传统晶体对称性中发现具有独特性质的范德华材料。
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引用次数: 0
Evidence for time-reversal symmetry-breaking kagome superconductivity 打破时间反转对称的可果美超导电性证据
IF 41.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-28 DOI: 10.1038/s41563-024-01995-w
Hanbin Deng, Guowei Liu, Z. Guguchia, Tianyu Yang, Jinjin Liu, Zhiwei Wang, Yaofeng Xie, Sen Shao, Haiyang Ma, William Liège, Frédéric Bourdarot, Xiao-Yu Yan, Hailang Qin, C. Mielke, R. Khasanov, H. Luetkens, Xianxin Wu, Guoqing Chang, Jianpeng Liu, Morten Holm Christensen, Andreas Kreisel, Brian Møller Andersen, Wen Huang, Yue Zhao, Philippe Bourges, Yugui Yao, Pengcheng Dai, Jia-Xin Yin

Superconductivity and magnetism are often antagonistic in quantum matter, although their intertwining has long been considered in frustrated-lattice systems. Here we utilize scanning tunnelling microscopy and muon spin resonance to demonstrate time-reversal symmetry-breaking superconductivity in kagome metal Cs(V, Ta)3Sb5, where the Cooper pairing exhibits magnetism and is modulated by it. In the magnetic channel, we observe spontaneous internal magnetism in a fully gapped superconducting state. Under the perturbation of inverse magnetic fields, we detect a time-reversal asymmetrical interference of Bogoliubov quasi-particles at a circular vector. At this vector, the pairing gap spontaneously modulates, which is distinct from pair density waves occurring at a point vector and consistent with the theoretical proposal of an unusual interference effect under time-reversal symmetry breaking. The correlation between internal magnetism, Bogoliubov quasi-particles and pairing modulation provides a chain of experimental indications for time-reversal symmetry-breaking kagome superconductivity.

在量子物质中,超导性和磁性通常是对立的,尽管在挫折晶格系统中它们的交织早已被考虑。在这里,我们利用扫描隧穿显微镜和μ介子自旋共振证明了卡戈枚金属 Cs(V,Ta)3Sb5 中的时间反转对称破缺超导性,其中库珀配对显示出磁性并受其调制。在磁通道中,我们观察到全间隙超导态的自发内部磁性。在反向磁场的扰动下,我们在一个圆形矢量处探测到了波哥留布夫准粒子的时间反转非对称干涉。在该矢量处,配对间隙自发地发生调制,这与发生在点矢量处的配对密度波不同,与理论上提出的时间逆对称破缺下的异常干涉效应相一致。内磁、波哥留波夫准粒子和配对调制之间的相关性为时间逆对称破缺的可果美超导性提供了一连串的实验迹象。
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引用次数: 0
A metastable pentagonal 2D material synthesized by symmetry-driven epitaxy 通过对称驱动外延合成的可蜕变五边形二维材料。
IF 37.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-27 DOI: 10.1038/s41563-024-01987-w
Lina Liu, Yujin Ji, Marco Bianchi, Saban M. Hus, Zheshen Li, Richard Balog, Jill A. Miwa, Philip Hofmann, An-Ping Li, Dmitry Y. Zemlyanov, Youyong Li, Yong P. Chen
Most two-dimensional (2D) materials experimentally studied so far have hexagons as their building blocks. Only a few exceptions, such as PdSe2, are lower in energy in pentagonal phases and exhibit pentagons as building blocks. Although theory has predicted a large number of pentagonal 2D materials, many of these are metastable and their experimental realization is difficult. Here we report the successful synthesis of a metastable pentagonal 2D material, monolayer pentagonal PdTe2, by symmetry-driven epitaxy. Scanning tunnelling microscopy and complementary spectroscopy measurements are used to characterize this material, which demonstrates well-ordered low-symmetry atomic arrangements and is stabilized by lattice matching with the underlying Pd(100) substrate. Theoretical calculations, along with angle-resolved photoemission spectroscopy, reveal monolayer pentagonal PdTe2 to be a semiconductor with an indirect bandgap of 1.05 eV. Our work opens an avenue for the synthesis of pentagon-based 2D materials and gives opportunities to explore their applications such as multifunctional nanoelectronics. A metastable pentagonal PdTe2 monolayer has been synthesized through symmetry-driven epitaxy, utilizing lattice matching with a Pd(100) substrate. The lattices, phonons and electronic structures of this phase have been studied.
迄今为止,实验研究的大多数二维(2D)材料都以六边形为构件。只有 PdSe2 等少数例外,其五边形相的能量较低,并以五角星为构件。虽然理论上已经预言了大量的五边形二维材料,但其中很多都是易变的,而且很难在实验中实现。在此,我们报告了通过对称驱动外延成功合成了一种可蜕变的五边形二维材料--单层五边形 PdTe2。扫描隧穿显微镜和互补光谱测量被用来描述这种材料的特性,它展示了井然有序的低对称原子排列,并通过与底层钯(100)基底的晶格匹配而得到稳定。理论计算和角度分辨光发射光谱显示,单层五边形 PdTe2 是一种间接带隙为 1.05 eV 的半导体。我们的研究为五边形二维材料的合成开辟了一条途径,并为探索它们在多功能纳米电子学等方面的应用提供了机会。
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引用次数: 0
Perovskite waveguides with predefined shapes for nonlinear photonics 用于非线性光子学的具有预定形状的 Perovskite 波导。
IF 37.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-27 DOI: 10.1038/s41563-024-01994-x
A versatile microfluidic approach is used to fabricate microstructures of arbitrarily predefined shapes from CsPbBr3 monocrystals. The resulting perovskite structures demonstrate waveguiding capabilities and edge lasing from polariton condensates with highly coherent emitted light. This approach is a first step towards perovskite-based nonlinear integrated photonics.
利用多功能微流体方法从 CsPbBr3 单晶中制造出任意预定形状的微结构。由此产生的过氧化物结构展示了波导能力,以及来自极化子凝聚物的边缘激光和高度相干的发射光。这种方法为实现基于包晶的非线性集成光子学迈出了第一步。
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引用次数: 0
Twist-angle-tunable spin texture in WSe2/graphene van der Waals heterostructures WSe2/ 石墨烯范德华异质结构中的扭角可调自旋纹理。
IF 37.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-27 DOI: 10.1038/s41563-024-01985-y
Haozhe Yang, Beatriz Martín-García, Jozef Kimák, Eva Schmoranzerová, Eoin Dolan, Zhendong Chi, Marco Gobbi, Petr Němec, Luis E. Hueso, Fèlix Casanova
Twist engineering has emerged as a powerful approach for modulating electronic properties in van der Waals heterostructures. While theoretical works have predicted the modulation of spin texture in graphene-based heterostructures by twist angle, experimental studies are lacking. Here, by performing spin precession experiments, we demonstrate tunability of the spin texture and associated spin–charge interconversion with twist angle in WSe2/graphene heterostructures. For specific twist angles, we detect a spin component radial with the electron’s momentum, in addition to the standard orthogonal component. Our results show that the helicity of the spin texture can be reversed by twist angle, highlighting the critical role of the twist angle in the spin–orbit properties of WSe2/graphene heterostructures and paving the way for the development of spin-twistronic devices. The authors experimentally demonstrate twist-angle modulation of the spin texture in graphene-based heterostructures.
扭转工程已成为调制范德华异质结构电子特性的有力方法。虽然理论研究已经预测了扭转角度对石墨烯基异质结构中自旋纹理的调制,但还缺乏实验研究。在这里,我们通过自旋前驱实验证明了 WSe2/石墨烯异质结构中自旋纹理和相关自旋电荷互转随扭转角度的可调性。在特定的扭转角度下,除了标准的正交分量外,我们还检测到与电子动量成径向的自旋分量。我们的研究结果表明,自旋纹理的螺旋度可以通过扭转角度发生逆转,这凸显了扭转角度在 WSe2/ 石墨烯异质结构的自旋轨道特性中的关键作用,并为开发自旋扭转器件铺平了道路。
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引用次数: 0
Free-space direct nanoscale 3D printing of metals and alloys enabled by two-photon decomposition and ultrafast optical trapping 利用双光子分解和超快光学捕获技术实现金属和合金的自由空间直接纳米级三维打印
IF 41.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-08-21 DOI: 10.1038/s41563-024-01984-z
Yaoyu Wang, Chenqi Yi, Wenxiang Tian, Feng Liu, Gary J. Cheng

Nanoscale three-dimensional (3D) printing of metals and alloys has faced challenges in speed, miniaturization and deficiency in material properties. Traditional nanomanufacturing relies on lithographic methods with material constraints, limited resolution and slow layer-by-layer processing. This work introduces polymer-free techniques using two-photon decomposition and optical force trapping for free-space direct 3D printing of metals, metal oxides and multimetallic alloys with resolutions beyond optical limits. This method involves the two-photon decomposition of metal atoms from precursors, rapid assembly into nanoclusters via optical forces and ultrafast laser sintering, yielding dense, smooth nanostructures. Enhanced near-field optical forces from laser-induced localized surface plasmon resonance facilitate nanocluster aggregation. Our approach eliminates the need for organic materials, layer-by-layer printing and complex post-processing. Printed Mo nanowires show an excellent mechanical performance, closely resembling the behaviour of single crystals, while Mo–Co–W alloy nanowires outperform Mo nanowires. This innovation promises the customizable 3D nanoprinting of high-quality metals and metal oxides, impacting nanoelectronics, nanorobotics and advanced chip manufacturing.

金属和合金的纳米级三维(3D)打印在速度、微型化和材料性能缺陷方面面临挑战。传统的纳米制造依赖于光刻方法,这种方法存在材料限制、分辨率有限和逐层加工速度慢等问题。这项工作介绍了使用双光子分解和光学力捕捉的无聚合物技术,用于金属、金属氧化物和多金属合金的自由空间直接三维打印,分辨率超过光学极限。该方法包括双光子分解前驱体中的金属原子、通过光学力快速组装成纳米团簇以及超快激光烧结,从而产生致密、光滑的纳米结构。激光诱导的局部表面等离子体共振增强了近场光学力,促进了纳米团簇的聚集。我们的方法无需使用有机材料、逐层打印和复杂的后处理。打印出的钼纳米线显示出卓越的机械性能,与单晶体的性能十分相似,而钼-钴-钨合金纳米线的性能则优于钼纳米线。这项创新有望实现高质量金属和金属氧化物的可定制三维纳米打印,对纳米电子学、纳米机器人学和先进芯片制造产生影响。
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引用次数: 0
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Nature Materials
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