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Core-shell quantum dot-enabled monolayer MoS2 memories with high endurance 具有高耐久性的核壳量子点支持的单层MoS2存储器
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102488
Yuanyuan Qiu (裘元园) , Zhuo Zhao (赵卓) , Shuo Qiao (乔朔) , Yue Lu (鲁跃) , Chaodan Pu (濮超丹) , Qingqing Ji (纪清清)
Nonvolatile memories based on low-dimensional materials are pivotal for miniaturized data storage but face challenges in endurance and charge retention. We report a mixed-dimensional memory architecture integrating monolayer MoS2 with CdSe@CdS core-shell quantum dots (QDs) to address these limitations. By synthesizing polyhedral QDs with facet-engineered surfaces and electrochemically inert passivating ligands, interfacial defects are substantially minimized, enabling efficient charge confinement within CdSe cores via Fowler-Nordheim tunneling. The optimized heterostructure device demonstrates a memory window of 140 V, an on/off ratio of 106, endurance exceeding 5 × 104 cycles, and 96.5% charge retention over 10 years—outperforming previously reported QD-based memories. Furthermore, the cascaded charge transfer mechanism (MoS2→CdS→CdSe), corroborated by electrical measurements, highlights the critical role of synergistic structural and surface optimization in suppressing charge leakage. This work establishes a scalable platform combining 2D semiconductors and defect-engineered QDs, offering insights into charge dynamics and advancing the development of high-performance, nanoscale nonvolatile memories.
基于低维材料的非易失性存储器是小型化数据存储的关键,但在耐用性和电荷保持方面面临挑战。我们报告了一种将单层MoS2与CdSe@CdS核壳量子点(QDs)集成在一起的混合维存储架构,以解决这些限制。通过合成具有面工程表面和电化学惰性钝化配体的多面体量子点,可以大大减少界面缺陷,从而通过Fowler-Nordheim隧道在CdSe核心内实现有效的电荷约束。优化后的异质结构器件的记忆窗口为140 V,开关比为106,续航时间超过5 × 104次,超过10年的电荷保留率为96.5%,优于先前报道的基于量子点的存储器。此外,电测量证实了级联电荷转移机制(MoS2→CdS→CdSe),强调了协同结构和表面优化在抑制电荷泄漏中的关键作用。这项工作建立了一个结合二维半导体和缺陷工程量子点的可扩展平台,提供了对电荷动力学的见解,并推进了高性能、纳米级非易失性存储器的发展。
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引用次数: 0
Entropy-guided design of thermoelectric properties in multi-component compounds 多组分化合物热电性质的熵导设计
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102625
Cheenepalli Nagarjuna, Peyala Dharmaiah, Babu Madavali, Murali Bissannagari, Saikat Shyamal, Weizong Bao, Soon-Jik Hong, Jinxue Ding, Xufei Fang, Byungmin Ahn, Wenjun Lu, BinBin He
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引用次数: 0
Self-powered functional hydrogel bioelectronics: From material design to biomedical applications 自供电功能水凝胶生物电子学:从材料设计到生物医学应用
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102461
Chuanwei Zhi , Cong Wang , Hanbai Wu , Chaofei Guo , Xiong Zhou , Shuo Shi , Yifan Si , Jinlian Hu
Hydrogels, prized for tissue-like properties and biointegration, are crucial for sustainable, self-powered wearable/implantable devices. However, adoption is hindered by low energy output, robustness issues, integration complexity, environmental sensitivity, and biosafety concerns. This review synthesizes recent advances in hydrogel-based piezoelectric and triboelectric nanogenerators (PENGs/TENGs). It outlines their fundamental principles and different design architectures. Key synthetic and natural polymer properties are examined, summarizing material/structural innovations to boost energy output while discussing potential trade-offs. Critical hydrogel properties for biomedical use, tunable adhesion, mechanics, self-healing, environmental adaptability, biocompatibility and degradation, and injectability are systematically reviewed, detailing current design strategies. Practical applications explored include wearable energy harvesters, human-computer interfaces, physiological monitoring, and bioelectronic medicine, with discussions of device implementation and clinical translation. Finally, the review covers remaining research gaps and emerging directions in self-powered functional hydrogel bioelectronics, providing insights to advance soft bioelectronics and self-powered wearables.
水凝胶因其组织样特性和生物整合而备受赞誉,对于可持续、自供电的可穿戴/植入式设备至关重要。然而,低能量输出、鲁棒性问题、集成复杂性、环境敏感性和生物安全问题阻碍了该技术的采用。本文综述了基于水凝胶的压电和摩擦电纳米发电机(PENGs/TENGs)的最新进展。它概述了它们的基本原理和不同的设计架构。研究了关键的合成和天然聚合物特性,总结了材料/结构创新,以提高能源输出,同时讨论了潜在的权衡。本文系统地回顾了生物医学用水凝胶的关键特性、可调粘附性、力学、自愈性、环境适应性、生物相容性和降解以及可注射性,详细介绍了当前的设计策略。实际应用包括可穿戴式能量采集器、人机界面、生理监测和生物电子医学,并讨论了设备的实现和临床翻译。最后,综述了自供电功能水凝胶生物电子学的剩余研究空白和新兴方向,为推进软生物电子学和自供电可穿戴设备提供了见解。
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引用次数: 0
Conductive polymeric gels for triboelectric tactile perception 用于摩擦电触觉感知的导电聚合物凝胶
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102612
Jinlong Wang , Yanhua Liu , Shuangxi Nie
With tactile perception evolving toward softer, self-recovering, and self-powered systems, conductive polymeric gels are becoming key material platforms. A recently reported gel that restores conductivity after solvent loss offers new avenues for improving durability and recovering performance in triboelectric tactile sensors.
随着触觉感知向更柔软、自恢复和自供电系统发展,导电聚合物凝胶正成为关键的材料平台。最近报道的一种凝胶可以在溶剂损失后恢复导电性,为提高摩擦电触觉传感器的耐用性和恢复性能提供了新的途径。
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引用次数: 0
Photo-magnetically actuated biohybrid microrobots 光磁驱动的生物混合微型机器人
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102531
Víctor de la Asunción-Nadal , Michaela Vojníková , Jack Latella , Chuanrui Chen , An-Yi Chang , Robert Kobrin , Zhenning Zhou , Yihan Che , Zbyněk Heger , Joseph Wang
Microscale biohybrid robots harnessing naturally motile cells offer autonomous long-lasting propulsion and biocompatibility. Yet, precisely directing and controlling their motion remains challenging. Here we demonstrate independent and simultaneous control over different types of biohybrid microrobots and complex motion pattern generation by combining multiple inputs into a single microrobot. We present a novel motion control mechanism for simultaneous phototactic and magnetotactic operation of biohybrid microrobots based on wild-type and blind Chlamydomonas reinhardtii (CR) modified with gelatin-Fe3O4 nanoparticles (gel-SPION). As a result, we developed methods to precisely control the motion of three distinct biohybrids with combined light and magnetic fields. By applying a combination of light and magnetic fields, different biohybrid strains can be sorted in different directions and controlled independently by decoupling the biohybrid magnetotactic and phototactic responses. This work lays the foundation for programmable, selective manipulation of biohybrid microrobots in variable environments, paving the way for advanced control strategies.
微型生物混合机器人利用自然运动细胞提供自主持久推进和生物相容性。然而,精确地指导和控制它们的运动仍然是一个挑战。在这里,我们展示了对不同类型的生物混合微型机器人的独立和同时控制,以及通过将多个输入组合到一个微型机器人中来生成复杂的运动模式。基于明胶- fe3o4纳米粒子修饰的野生型和盲型莱茵衣藻(CR) (gel-SPION),提出了一种同时进行趋光和趋磁操作的生物混合微型机器人运动控制机制。因此,我们开发了一种方法,通过结合光和磁场来精确控制三种不同的生物杂交体的运动。在光、磁场联合作用下,通过解耦生物杂交种的趋磁和趋光响应,可以实现不同生物杂交种在不同方向上的分选和独立控制。这项工作为可变环境下生物混合微型机器人的可编程、选择性操作奠定了基础,为先进的控制策略铺平了道路。
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引用次数: 0
Revolutionizing sustainability through atmospheric moisture sorbents 通过大气吸湿剂革新可持续性
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102536
Zhuorui Han , Xiaochen Zhang , Xianfeng Peng , Zisheng Luo , Xingyu Lin
Atmospheric moisture sorbents (AMSs) possess ideal structures that enable spontaneous absorption of substantial amounts of moisture from ambient environment. This passive adsorption process requires no additional energy input and is considered as a clean technology for sustainability. Characterized by their environmental friendliness, versatility, and scalability, AMSs have enabled sustainable applications across the agriculture, food, environment, and energy nexus. In this review, the interaction mechanism between AMSs and moisture is systematically revealed from multiple perspectives. Then we comprehensively assess AMSs-enabled sustainability across agricultural productivity, food security, environmental resilience, and energy transition. In order to meet sustainability objectives, particular emphasis is placed on evaluating the efficiency, feasibility, and cost-effectiveness of practical applications based on comprehensive analysis of material compositions, structural characteristics, and performance metrics. In the future, AMSs are expected to play a pivotal role in addressing critical challenges in agriculture, food, environment, and energy systems, particularly in resource-constrained regions, while contributing to the global strategic goals of energy conservation and carbon neutrality.
大气吸湿剂(ams)具有理想的结构,能够从周围环境中自发吸收大量的水分。这种被动吸附过程不需要额外的能量输入,被认为是一种可持续的清洁技术。ams的特点是环境友好、多功能性和可扩展性,使农业、食品、环境和能源领域的可持续应用成为可能。本文从多个角度系统地揭示了ams与水分的相互作用机制。然后,我们全面评估了农业生产力、粮食安全、环境恢复力和能源转型等领域的ams可持续性。为了满足可持续发展的目标,特别强调在材料成分、结构特征和性能指标的综合分析的基础上评估实际应用的效率、可行性和成本效益。未来,预计自动农业系统将在应对农业、粮食、环境和能源系统的重大挑战方面发挥关键作用,特别是在资源受限地区,同时为实现节能和碳中和的全球战略目标作出贡献。
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引用次数: 0
Modulating diffusion kinetics and interfacial stability via in situ constructed fluoronitrided interfaces for highly durable sodium-metal batteries 通过原位构建的高耐用钠金属电池氟氮化界面调节扩散动力学和界面稳定性
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102492
Yangjie Liu , Huiling Fang , Lu Zhang , Qirui Wu , Mujtaba Aminu Muhammad , Junxiang Chen , Hongbing Zhan , Xiang Hu , Lihong Xu , Zhenhai Wen
Sodium-metal anodes hold great promise for high-energy-density sodium-based batteries, yet their application is hindered by poor cycling stability and safety concerns arising from interfacial instability and uncontrolled dendritic growth. Herein, we propose a multifunctional sodium-metal composite anode based on 3D porous carbon framework embedded with molybdenum nitride (MoN) nanoparticles. During sodiation, MoN undergoes in situ conversion to metallic Mo and Na3N while catalyzing NaPF6 decomposition to form NaF, leading to a self-evolved fluoronitrided interphase (Na3N/NaF). This robust SEI combines mechanical resilience, high surface energy, and superior Na+ conductivity, ensuring uniform deposition and dendrite suppression. Consequently, the symmetric cell achieves low overpotential and exceptional cycling stability over 2,000 h at 3 mA cm−2. When paired with a Na3V2(PO4)3 cathode, the full-battery presents remarkable electrochemical performance with an energy density of 265 Wh kg−1. This strategy stabilizes sodium-metal interfaces and paves a promising route toward high-performance and durable sodium-metal batteries for sustainable energy storage.
钠金属阳极在高能量密度钠基电池中具有很大的应用前景,但由于界面不稳定和不受控制的枝晶生长引起的循环稳定性差和安全性问题,阻碍了它们的应用。在此,我们提出了一种基于嵌入氮化钼纳米粒子的三维多孔碳框架的多功能钠-金属复合阳极。在钠化过程中,MoN在原位转化为金属Mo和Na3N,同时催化NaPF6分解形成NaF,导致自进化的氟氮化界面(Na3N/NaF)。这种坚固的SEI结合了机械弹性、高表面能和优异的Na+导电性,确保了均匀的沉积和枝晶抑制。因此,对称电池在3ma cm - 2下实现了低过电位和超过2000小时的卓越循环稳定性。当与Na3V2(PO4)3阴极配对时,该电池的能量密度达到265 Wh kg−1,具有良好的电化学性能。这一策略稳定了钠-金属界面,为高性能和耐用的钠-金属电池的可持续能量存储铺平了一条有希望的道路。
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引用次数: 0
Aerosol-based combinatorial printing of cholesteric liquid crystal elastomers with tunable and pixelated structural colors 具有可调和像素化结构颜色的胆甾液晶弹性体的气溶胶基组合印刷
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102495
Shangsong Li , Kaidong Song , Yuxuan Liao , Yipu Du , Zhengdan Lin , Kun-Yu Wang , Yanliang Zhang , Shu Yang
Structural colors in living creatures often feature diverse gradient color patterns composed of (sub)micron-sized pixels, leading to dynamic and complex visual signals. However, conventional single-material printing of artificial structural colors yields only one color at a time, limiting spatial resolution and tunability. Here, we report a combinatorial aerosol printing (CAP) strategy, a multi-ink variant of aerosol jet printing, to produce pixelated mechanochromic cholesteric liquid crystal elastomers (CLCEs) with ≈15 μm line resolution and 1.1 μm thickness. By co-delivering and mixing aerosolized inks in situ, CAP enables continuous compositional gradients within individual pixels, yielding high-saturation colors with tunable helical pitch and Young’s modulus. Further, CLCE patterns can be directly printed on curved substrates, surpassing constraints of traditional methods. The ability to tailor optical and mechanical properties at high resolution establishes a versatile platform for mechanochromic materials, with applications in responsive displays, QR coding, biomimetic camouflage, and wearable photonic sensors.
生物的结构色通常具有由(亚)微米大小的像素组成的多种渐变颜色图案,导致动态和复杂的视觉信号。然而,传统的人工结构色单材料印刷一次只能产生一种颜色,限制了空间分辨率和可调性。在这里,我们报告了一种组合气溶胶打印(CAP)策略,一种多油墨气溶胶喷射打印的变体,以生产具有≈15 μm线分辨率和1.1 μm厚度的像素化机械变色胆甾液晶弹性体(clce)。通过在原位共同输送和混合雾化油墨,CAP可以在单个像素内实现连续的成分梯度,产生具有可调螺旋螺距和杨氏模量的高饱和度颜色。此外,CLCE图案可以直接印刷在弯曲的基板上,超越了传统方法的限制。在高分辨率下定制光学和机械性能的能力为机械变色材料建立了一个多功能平台,应用于响应式显示、QR编码、仿生伪装和可穿戴光子传感器。
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引用次数: 0
From compute to content: Building an AI Wikipedia for reliable and efficient artificial intelligence 从计算到内容:为可靠和高效的人工智能构建一个人工智能维基百科
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102607
Dong Zhang , Xuanzhou Chen
Computation-only scaling is delivering diminishing returns because errors persist. We propose a shared, expert-curated “AI Wikipedia”: a common knowledge base with clear tags, schemas, and provenance that systems can retrieve and reference, making generated content more factual, efficient, and easy to audit in any field.
由于错误持续存在,只进行计算的扩展带来的收益正在递减。我们提出了一个共享的、专家策划的“人工智能维基百科”:一个具有清晰标签、模式和来源的公共知识库,系统可以检索和引用,使生成的内容在任何领域都更加真实、高效和易于审核。
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引用次数: 0
Emerging high-entropy materials for rechargeable batteries 用于可充电电池的新兴高熵材料
IF 17.5 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-04 DOI: 10.1016/j.matt.2025.102556
Youcun Bai , Heng Zhang , Yuehao Gu , Xunzhu Zhou , Jiazhao Wang , Wenhao Liang , Shixue Dou , Lin Li
As a key component of rechargeable batteries, electrode materials significantly influence their electrochemical performance. However, existing electrode materials fail to meet the growing demands of practical applications, posing a major obstacle to advancing rechargeable battery technology. In recent years, high-entropy materials (HEMs) with unique structural characteristics have been considered as promising candidates for enhancing the electrochemical performance of rechargeable batteries. In this review, we systematically discuss the preparation methods, characterization technologies, electrochemical properties, and energy storage mechanisms of HEMs. In addition, we summarize the research progress of HEMs for application in rechargeable batteries, including alloys, oxides, sulfides, selenides, phosphates, Prussian blue analogs, and MXene. More importantly, we deeply analyze the relationship between the properties of HEMs and their potential applications in rechargeable batteries, as well as the remaining challenges of HEMs. This work provides strategic insights to accelerate the discovery of next-generation electrode materials for rechargeable batteries.
电极材料作为可充电电池的关键部件,对电池的电化学性能有着重要的影响。然而,现有的电极材料不能满足日益增长的实际应用需求,这是推动可充电电池技术发展的主要障碍。近年来,具有独特结构特性的高熵材料被认为是提高可充电电池电化学性能的有希望的候选材料。本文系统地介绍了HEMs的制备方法、表征技术、电化学性能和储能机理。此外,我们还总结了HEMs在可充电电池中的研究进展,包括合金、氧化物、硫化物、硒化物、磷酸盐、普鲁士蓝类似物和MXene等。更重要的是,我们深入分析了HEMs的性能与其在可充电电池中的潜在应用之间的关系,以及HEMs仍面临的挑战。这项工作为加速发现下一代可充电电池电极材料提供了战略见解。
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引用次数: 0
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