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Real‐Time Observation of Thermal Surface Recovery in SrVO 3 SrVO 3热表面恢复的实时观测
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-16 DOI: 10.1002/aelm.70541
Amit Cohen, Jonathan Ludwick, Ward Yahya, Maria Baskin, Lishai Shoham, Tyson C. Back, Lior Kornblum
Correlated oxides are emerging materials with a broad range of applications in next‐generation devices, most recently as attractive, earth‐abundant transparent conductive electrodes for photovoltaics and electro‐optic devices. SrVO 3 (SVO), a model correlated metal and a promising transparent conducting oxide, develops a several‐nanometer‐thick V 5 + near‐surface region (NSR) under ambient conditions. This oxidized layer obscures the intrinsic correlated‐metallic V 4 + character and limits both fundamental studies of the physics and the material's integration into electronic devices. Here, we demonstrate a direct and controllable approach for recovering the metallic SVO by thermally reducing the NSR under ultra‐high vacuum. Real‐time in situ X‐ray photoelectron spectroscopy reveals a sharp transformation from a V 5 + ‐dominated surface to mixed valence states, dominated by V 4 + (∼65% of the spectral weight), and a recovery of its metallic character. This is compared with a comprehensive ex situ analysis, suggesting this transformation is accompanied by mass redistribution and partial oxygen loss, leading to nanoscale surface reorganization and modest lattice expansion without loss of perovskite crystallographic integrity. These findings establish a practical method for obtaining predominantly V 4 + SVO surfaces without protective capping layers, a capability that expands the engineering and design space of correlated oxides for functional devices.
相关氧化物是一种新兴材料,在下一代器件中有着广泛的应用,最近被用作光伏和电光器件中具有吸引力的、含土丰富的透明导电电极。srvo3 (SVO)是一种模型相关金属,是一种很有前途的透明导电氧化物,在环境条件下形成了几纳米厚的v5 +近表面区域(NSR)。这种氧化层掩盖了固有的相关金属v4 +特性,限制了物理学的基础研究和材料集成到电子器件中。在这里,我们展示了一种在超高真空下通过热降低NSR来回收金属SVO的直接和可控的方法。实时原位X射线光电子能谱显示,从以v5 +为主的表面急剧转变为以v4 +为主的混合价态(约占光谱质量的65%),并恢复了其金属特征。这与全面的非原位分析进行了比较,表明这种转变伴随着质量再分配和部分氧损失,导致纳米级表面重组和适度的晶格膨胀,而不会损失钙钛矿晶体完整性。这些发现建立了一种实用的方法,可以在没有保护盖层的情况下获得主要的v4 + SVO表面,这一能力扩大了功能器件相关氧化物的工程和设计空间。
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引用次数: 0
Transparent and Flexible Broadband Microwave Absorber Based on a Nested Open‐Ring Metallic Mesh Architecture 基于嵌套开环金属网结构的透明柔性宽带微波吸收器
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-15 DOI: 10.1002/aelm.70608
Zhouying Jiang, Yuxi Hou, Mengnan Wang, Su Shen, Yan‐Hua Liu
Transparent and flexible microwave absorbers (TFMAs) are highly desirable for next‐generation electromagnetic stealth and shielding systems that demand conformal integration onto curved or deformable platforms, such as aircraft radomes, flexible displays, and wearable optoelectronic devices. However, most existing transparent absorbers rely on rigid substrates or brittle conductive layers, which are fundamentally incompatible with flexible and conformal applications. In this work, we propose an all‐mesh‐based multilayer TFMA that consists of a nested double open‐ring resonant layer formed by metallic meshes and a mesh‐covered reflective backing. Unlike continuous conductive films, the subwavelength mesh topology sustains intense localized electromagnetic resonance while permitting high visible transmission. This design enables a broadband absorption exceeding 90% across 4.9–12.3 GHz, covering both C‐ and X‐bands, and simultaneously exhibits an average visible transmittance of 75.8% and excellent mechanical flexibility. Moreover, the absorber delivers robust polarization and angle‐insensitive performance under oblique incidence, and retains over 80% absorption efficiency after rigorous static and cyclic bending tests, confirming exceptional mechanical durability. This work establishes a scalable design strategy for transparent microwave absorbers based on mesh‐engineered electromagnetic architectures, offering a promising pathway toward conformal electromagnetic protection compatible with optoelectronic and curved platforms.
透明和柔性微波吸收器(tfma)是下一代电磁隐身和屏蔽系统的理想选择,这些系统需要保形集成到弯曲或可变形的平台上,如飞机天线罩,柔性显示器和可穿戴光电设备。然而,大多数现有的透明吸收剂依赖于刚性衬底或脆性导电层,这从根本上与柔性和保形应用不相容。在这项工作中,我们提出了一种基于全网格的多层TFMA,它由由金属网格形成的嵌套双开环谐振层和覆盖网格的反射衬底组成。与连续导电薄膜不同,亚波长网状拓扑结构在允许高可见透射的同时保持强烈的局部电磁共振。该设计使4.9-12.3 GHz的宽带吸收超过90%,覆盖C -和X -波段,同时具有75.8%的平均可见光透过率和优异的机械灵活性。此外,吸收器在斜入射下具有强大的极化和角度不敏感性能,并且在严格的静态和循环弯曲测试后保持超过80%的吸收效率,证实了卓越的机械耐久性。这项工作建立了一种基于网格工程电磁结构的透明微波吸收器的可扩展设计策略,为与光电和弯曲平台兼容的共形电磁保护提供了一条有前途的途径。
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引用次数: 0
Perspective: Quantum Computing on Magnetic Racetrack 视角:磁赛道上的量子计算
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-15 DOI: 10.1002/aelm.70614
Ji Zou, Jelena Klinovaja, Daniel Loss
Magnetic domain walls have long been pursued as carriers of classical information for storage and processing. With the ability to create, control, and probe domain walls at the nanoscale, they are recently recognized as an ideal platform for studying macroscopic quantum effects and provide a natural blueprint for building scalable quantum computing architectures. In particular, the experimentally demonstrated high mobility of domain walls makes them not only suitable as stationary qubits but also as flying qubits, which may offer advantages over currently explored quantum computing platforms. In this Perspective, we outline our current understanding of the essential ingredients and key requirements for realizing universal quantum computation based on magnetic domain walls. We highlight promising concrete material platforms and identify the experiments that are still needed to advance this concept. We also discuss the potential challenges and point to new opportunities in this emerging research direction at the interface between magnetism and quantum information science.
磁畴壁作为经典信息存储和处理的载体一直受到人们的关注。由于能够在纳米尺度上创建、控制和探测畴壁,它们最近被认为是研究宏观量子效应的理想平台,并为构建可扩展的量子计算架构提供了自然蓝图。特别是,实验证明了域壁的高迁移性,使它们不仅适合作为静止量子比特,也适合作为飞行量子比特,这可能比目前探索的量子计算平台提供优势。在这个观点中,我们概述了我们目前对实现基于磁畴壁的通用量子计算的基本成分和关键要求的理解。我们强调了有前途的混凝土材料平台,并确定了仍需要推进这一概念的实验。我们还讨论了磁学和量子信息科学之间的潜在挑战,并指出了这一新兴研究方向的新机遇。
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引用次数: 0
Towards Ideal Electron‐Transporting Transistor Characteristics in Polymer Semiconductors in Ambient Air 环境空气中聚合物半导体理想电子输运晶体管特性的研究
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-14 DOI: 10.1002/aelm.70599
Hio‐Ieng Un, Miao Xiong, Yang Lu, Chi‐Yuan Yang, Tian‐Yu Zhang, Ze‐Fan Yao, Jie‐Yu Wang, Jian Pei
The coexistence of high mobility and ideal current–voltage transistor characteristics is highly desirable for real‐work applications of field‐effect transistors. However, very few high‐mobility polymer transistors can exhibit reliability factors >70%, and even rarer for electron‐transporting devices. In this work, we report a coexistence of a reliability factor of 90% and high mobility of 0.6 cm 2 V −1 s −1 in FBDPPV‐based transistors and, more importantly, systematically investigate the origin by combining optical and microstructural characterizations and transport physics study. We found that in this rigid, coplanar, distortion‐free polymer FBDPPV, efficient charge transport that induces high mobility and near‐ideal transistor behaviors is supported by efficient intrachain transport and limited by energetic disorder along the interchain transport pathway consisting of disorderly connected very small grains. We also compare the structure‐property relationship of FBDPPV with some benchmark high‐mobility polymers and provide insights into rational design strategies for achieving the coexistence of high mobility and ideal current–voltage transistor characteristics.
高迁移率和理想的电流电压晶体管特性的共存对于场效应晶体管的实际工作应用是非常理想的。然而,很少有高迁移率聚合物晶体管能够表现出70%的可靠性系数,对于电子传输器件来说就更罕见了。在这项工作中,我们报告了基于FBDPPV的晶体管中90%的可靠性因子和0.6 cm 2 V−1 s−1的高迁移率共存,更重要的是,通过结合光学和微结构表征以及输运物理研究,系统地研究了起源。我们发现,在这种刚性、共面、无畸变的聚合物FBDPPV中,有效的电荷传输诱导了高迁移率和接近理想的晶体管行为,这是由有效的链内传输支持的,并受到由无序连接的非常小的颗粒组成的链间传输途径的能量无序的限制。我们还比较了FBDPPV与一些基准高迁移率聚合物的结构-性能关系,并为实现高迁移率和理想电流-电压晶体管特性共存的合理设计策略提供了见解。
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引用次数: 0
Dynamic Landau–Khalatnikov Modeling of Ferroelectric Hafnium–Zirconium Oxides Across Volatile and Non‐Volatile Switching 铁电铪锆氧化物在挥发性和非挥发性开关中的动态Landau-Khalatnikov模型
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-13 DOI: 10.1002/aelm.70610
Davide Rossetti, Yichun Xu, Shiva Asapu, Taehwan Moon, Seung Ju Kim, Drake R. Austin, Ruoyu Zhao, Tong Wang, Jian Zhao, Brian M. Everhart, Michele Bonnin, Alon Ascoli, Fernando Corinto, Nicholas R. Glavin, R. Stanley Williams, J. Joshua Yang
The design of energy‐efficient neuromorphic devices demands compact, physically grounded models that seamlessly connect microscopic ferroelectric dynamics to macroscopic circuit behavior. Hafnium–zirconium oxides (, HZO) are compelling candidates owing to their CMOS compatibility, scalability below 10 nm, and tunable transition between ferroelectric and volatile responses. Yet, conventional first‐order Landau–Khalatnikov (LK) formulations cannot capture key experimental features such as negative differential capacitance, pseudo‐inductive transients, and leakage interplay. Here we introduce an extended LK framework incorporating inertial second‐order terms, nonlinear charge‐dependent damping, and a modular leakage branch. This unified, simulation‐ready model quantitatively reproduces experimental Q–V characteristics across Hf‐rich, equiatomic, and Zr‐rich HZO compositions, defining operational regimes from non‐volatile memory to volatile, reservoir‐like dynamics. By linking free‐energy landscapes to compact circuit representations, the approach establishes a predictive device–model–circuit co‐design framework that connects atomistic energetics with system‐level simulation, enabling composition‐specific design rules for scalable, low‐power neuromorphic architectures.
高效节能的神经形态器件的设计需要紧凑、物理接地的模型,将微观铁电动力学与宏观电路行为无缝连接。由于其CMOS兼容性、10nm以下的可扩展性以及铁电和挥发性响应之间的可调转换,铪锆氧化物(HZO)是令人信服的候选者。然而,传统的一阶Landau-Khalatnikov (LK)公式不能捕捉关键的实验特征,如负差分电容、伪电感瞬变和泄漏相互作用。在这里,我们引入了一个扩展的LK框架,包括惯性二阶项、非线性电荷相关阻尼和模块泄漏分支。这个统一的、可模拟的模型定量再现了富Hf、等原子和富Zr的HZO成分的实验Q-V特性,定义了从非易失性存储器到易失性储层式动力学的操作机制。通过将自由能景观与紧凑电路表示联系起来,该方法建立了一个预测性的器件-模型-电路协同设计框架,该框架将原子能量学与系统级仿真联系起来,为可扩展的低功耗神经形态架构提供了特定于组成的设计规则。
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引用次数: 0
Pairing Non‐Fullerene Acceptors With the Right Polymer: Impact of Phase Morphology and Short‐Range Transport on Charge Generation 非富勒烯受体与合适聚合物的配对:相形态和短程输运对电荷产生的影响
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-13 DOI: 10.1002/aelm.70581
Yufei Zhong, Gareth John Moore, Subhrangsu Mukherjee, Yanfang Geng, Nikolaos Droseros, Martina Causa’, Lee J. Richter, Dean M. DeLongchamp, Erjun Zhou, Natalie Banerji
Organic photovoltaics based on non‐fullerene acceptors (NFAs) have demonstrated high and rapidly increasing power conversion efficiency in recent years. Yet, the requirements for pairing NFAs with an optimal donor polymer remain unclear. To explore the desirable properties of polymers when combining them with NFAs, we herein study a representative NFA molecule combined with three different polymers. To mimic different phase morphologies, we compare bilayers to optimized blends with a three‐phase morphology (neat donor and acceptor regions coexisting with intermixed domains) and to ‘dilute‐donor’ and ‘dilute‐acceptor’ systems (completely intermixed scenario). The solar cell performance is related to the free charge generation efficiency probed by ultrafast transient and electro‐modulated absorption spectroscopy. We find that the free charge generation in the optimal polymer:NFA pair is highly resilient to the phase morphology. This blend benefits from a favorable kinetic competition between fast transport‐assisted charge separation (related to locally ordered polymer chains) and slow intrinsic recombination (related to a high‐lying charge transfer state, according to the energy gap law). These findings guide the molecular design of polymeric donors for efficient charge generation in NFA‐based photovoltaic blends.
近年来,基于非富勒烯受体(nfa)的有机光伏发电显示出高且快速增长的功率转换效率。然而,对nfa与最佳供体聚合物配对的要求仍不清楚。为了探索聚合物与NFA结合时的理想性能,我们在此研究了一个具有代表性的NFA分子与三种不同的聚合物结合。为了模拟不同的相形态,我们将双层结构与具有三相形态的优化混合物(整齐的供体和受体区域与混合结构域共存)和“稀释供体”和“稀释受体”体系(完全混合的情况)进行了比较。太阳能电池的性能与超快瞬态和电调制吸收光谱测量的自由电荷产生效率有关。我们发现在最佳的聚合物:NFA对中自由电荷的产生对相形态具有高度的弹性。这种混合受益于快速输运辅助电荷分离(与局部有序聚合物链有关)和缓慢的内在重组(根据能隙定律,与高电荷转移态有关)之间有利的动力学竞争。这些发现指导了在NFA基光伏共混物中高效产生电荷的聚合物供体的分子设计。
{"title":"Pairing Non‐Fullerene Acceptors With the Right Polymer: Impact of Phase Morphology and Short‐Range Transport on Charge Generation","authors":"Yufei Zhong, Gareth John Moore, Subhrangsu Mukherjee, Yanfang Geng, Nikolaos Droseros, Martina Causa’, Lee J. Richter, Dean M. DeLongchamp, Erjun Zhou, Natalie Banerji","doi":"10.1002/aelm.70581","DOIUrl":"https://doi.org/10.1002/aelm.70581","url":null,"abstract":"Organic photovoltaics based on non‐fullerene acceptors (NFAs) have demonstrated high and rapidly increasing power conversion efficiency in recent years. Yet, the requirements for pairing NFAs with an optimal donor polymer remain unclear. To explore the desirable properties of polymers when combining them with NFAs, we herein study a representative NFA molecule combined with three different polymers. To mimic different phase morphologies, we compare bilayers to optimized blends with a three‐phase morphology (neat donor and acceptor regions coexisting with intermixed domains) and to ‘dilute‐donor’ and ‘dilute‐acceptor’ systems (completely intermixed scenario). The solar cell performance is related to the free charge generation efficiency probed by ultrafast transient and electro‐modulated absorption spectroscopy. We find that the free charge generation in the optimal polymer:NFA pair is highly resilient to the phase morphology. This blend benefits from a favorable kinetic competition between fast transport‐assisted charge separation (related to locally ordered polymer chains) and slow intrinsic recombination (related to a high‐lying charge transfer state, according to the energy gap law). These findings guide the molecular design of polymeric donors for efficient charge generation in NFA‐based photovoltaic blends.","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"11 12 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2026-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
MoS 2 Memristors Made by Liquid–Liquid Interface Assembly and Ultraprecise Metal Printing 液-液界面组装和超精密金属打印制造的MoS 2忆阻器
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-13 DOI: 10.1002/aelm.70582
Miguel Franco, Daniel Neves, Dorina T. Papanastasiou, Jonas Deuermeier, Tomás Calmeiro, Tomás Mingates, Adam Kelly, Joseph Neilson, Eugénie Martinez, Zdeněk Sofer, Elvira Fortunato, Rodrigo Martins, Emanuel Carlos, Asal Kiazadeh
A cleanroom‐free process was developed for the fabrication of ultralow‐power resistive switching devices. Sub‐micron‐thick silver (Ag) electrodes are printed by XTPL's Ultraprecise Dispensing technology in a fully additive process. Two‐layer molybdenum disulfide (MoS 2 ) is used as the active layer, which was prepared and deposited by the Langmuir‐Schaefer technique. Devices with 30 × 30 µm 2 with volatile and non‐volatile operation were produced. These exhibit SET and RESET voltages of 0.32 ± 0.09 V and −0.29 ± 0.09 V, respectively, a memory window up to 10 6 , an endurance of 300 cycles achieved by voltage sweep, and stable operation under vacuum. The devices can retain the state for over 10 5 s. By employing high‐resolution printing techniques and an ultra‐conformable liquid‐based two‐dimensional materials deposition process, cost‐efficient and high‐performance resistive switching devices were fabricated for next‐generation computation and communication.
开发了一种制造超低功率电阻开关器件的无尘室工艺。亚微米厚的银(Ag)电极由XTPL的超精密点胶技术在全增材工艺中印刷。采用Langmuir - Schaefer技术制备两层二硫化钼(MoS 2)作为活性层。生产了具有易失性和非易失性操作的30 × 30µm2器件。这些器件的SET和RESET电压分别为0.32±0.09 V和- 0.29±0.09 V,记忆窗口高达10.6,电压扫描可实现300次循环,在真空下稳定工作。设备状态保持时间超过105s。通过采用高分辨率印刷技术和超符合的液体基二维材料沉积工艺,为下一代计算和通信制造了低成本和高性能的电阻开关器件。
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引用次数: 0
Enhanced Thermoelectric Performance of GeTe‐Sb 2 Te 3 Pseudo‐Binary Phase Change Material Through Stoichiometry Optimization 通过化学计量优化提高GeTe - sb2t3伪二元相变材料的热电性能
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-13 DOI: 10.1002/aelm.70609
Nur Qalishah Adanan, Sichao Li, Syed Zulfiqar Hussain Shah, Durga Venkata Maheswar Repaka, Joel K. W. Yang, Iris Nandhakumar, Kedar Hippalgaonkar, Sunmi Shin, Robert E. Simpson, Pawan Kumar
Pseudo‐Binary GeTe‐Sb 2 Te 3 materials have demonstrated promising thermoelectric performance in intermediate temperature (500‐800 K) range. In this work, by co‐sputtering of Ge 45 Te 52 S 3 and Sb 2 Te 3 a composition spreads with varying Ge:Sb:Te ratios were fabricated to identify specific composition regimes with the highest thermoelectric performance. From the thermoelectric measurements, (Ge 5 Sb 37 Te 58 ) demonstrated the highest power factor values. Thermal conductivity measurements were performed on the different compositions with higher power factor values. Maximum zT values ranging from 0.36 ± 0.08 to 0.81 ± 0.15 for samples Ge 9 Sb 33 Te 58 to Ge 5 Sb 37 Te 58 at 300°C were achieved. The co‐sputtering technique establishes an effective high‐throughput approach to systematically map the relationship between composition and thermoelectric properties across a wide range of compositions in a single deposition run.
伪二元GeTe - sb2 - Te - 3材料在中温(500 - 800 K)范围内表现出了良好的热电性能。在这项工作中,通过共溅射Ge 45 Te 52 S 3和Sb 2 Te 3 a,制备了具有不同Ge:Sb:Te比例的复合镀层,以确定具有最高热电性能的特定组合体系。从热电测量中,(Ge 5 Sb 37 Te 58)显示出最高的功率因数值。对功率因数值较高的不同成分进行了导热系数测量。在300℃下,g9 Sb 33 Te 58 ~ g5 Sb 37 Te 58样品的zT最大值为0.36±0.08 ~ 0.81±0.15。共溅射技术建立了一种有效的高通量方法,可以在单次沉积中系统地绘制大范围成分与热电性能之间的关系。
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引用次数: 0
Enabling Quantum-Compatible Nonvolatile Memory: Cryogenic Evaluation of 1T1R HfO2-Based RRAM From 300 to 1.5 K 实现量子兼容的非易失性存储器:从300到1.5 K的基于1T1R HfO 2的RRAM的低温评估
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-12 Epub Date: 2026-08-13 DOI: 10.1002/aelm.202500798
Emilio Pérez-Bosch Quesada, Alberto Mistroni, Ruolan Jia, Keerthi Dorai Swamy Reddy, Markus Fritscher, Felix Reichmann, Oliver Skibitzki, Juan Bautista Roldán, Helena Castán, Salvador Dueñas, Christian Wenger, Eduardo Pérez

To enable compact quantum computing systems, cryogenically compatible CMOS-based non-volatile memories are required. In this work, we investigate 1-transistor–1-resistor (1T1R) resistive random-access memory (RRAM) devices over an extended temperature range, including previously unexplored cryogenic regimes. To enhance storage density, we explore a multilevel-cell approach via multilevel programming. As temperature decreases, the low-resistance state (LRS) effective conductance increases, improving state separation but also leading to higher LRS currents and increased reset voltages required for reliable switching to the high-resistance state (HRS), resulting in incomplete filament rupture and a broader HRS distribution. Through independent characterization of the access nMOS transistor, we identify transistor temperature dependence as the dominant factor governing LRS evolution, while extraction of the intrinsic metal–insulator–metal (MIM) behavior reveals an opposite trend, with decreasing conductivity at lower temperatures. Based on these insights, we implement an optimized programming strategy for cryogenic operation by tuning the nMOS gate bias during set, reducing LRS currents, particularly in intermediate and high conductance states, while preserving state separation, narrowing the HRS distribution, and lowering reset voltages. Overall, this work establishes a robust and scalable approach for reliable 1T1R operation at cryogenic temperatures and provides a key step toward nonvolatile memory integration in quantum computing architectures.

为了实现紧凑的量子计算系统,需要低温兼容的基于CMOS的非易失性存储器。在这项工作中,我们在扩展的温度范围内研究了1 -晶体管- 1 -电阻(1T1R)电阻随机存取存储器(RRAM)器件,包括以前未探索的低温环境。为了提高存储密度,我们通过多层编程探索了一种多层单元方法。随着温度的降低,低阻状态(LRS)的有效电导增加,改善了状态分离,但也导致更高的LRS电流和更高的复位电压,这是可靠切换到高阻状态(HRS)所需的,导致灯丝不完全破裂和更宽的HRS分布。通过对nMOS晶体管的独立表征,我们确定了晶体管温度依赖性是控制LRS演变的主要因素,而提取金属-绝缘体-金属(MIM)的固有行为则揭示了相反的趋势,即在较低温度下电导率降低。基于这些见解,我们通过在设置过程中调整nMOS栅极偏置,减少LRS电流,特别是在中导和高导状态下,同时保持状态分离,缩小HRS分布,降低复位电压,实现了低温操作的优化编程策略。总的来说,这项工作为在低温下可靠的1T1R操作建立了一种强大且可扩展的方法,并为量子计算架构中的非易失性存储器集成提供了关键一步。
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引用次数: 0
Reconfigurable Ternary Logic-In-Memory With Organic Antiambipolar Transistor 可重构三元逻辑存储器与有机反双极性晶体管
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-10-12 Epub Date: 2026-08-20 DOI: 10.1002/aelm.70538
Ryoma Hayakawa, Taiga Kijima, Yuho Yamamoto, Yoichi Yamada, Yutaka Wakayama

We developed a reconfigurable ternary logic-in-memory (LIM) device based on an organic antiambipolar transistor and incorporating a gold floating gate into a hafnium oxide (HfO2) gate insulator. First, a standard ternary inverter was obtained with extremely low input and drain voltages (2 V) owing to the high dielectric constant of the HfO2 gate insulator. Three distinct output logic states (“2,” “1,” and “0”) were clearly obtained for the corresponding input logic states (“0,” “1,” and “2”). Then, the voltage transfer curve was laterally shifted up to 1.8 V by controlling the hole- and electron-injection processes into the floating gate, obtaining a ternary nonvolatile memory. This memory function realized versatile reconfigurable ternary inverter operations. Three ternary inverters, namely, standard, negative, and positive ternary inverters, were demonstrated in a single LIM device. Remarkably, these inverter operations were performed using the same input voltages and then electrically reconfigured by adjusting the charge condition (i.e., holes or electrons) of the floating gate. Our development seems promising for performing multivalued in-memory computing toward surpassing the capabilities of existing von Neumann systems.

我们开发了一种可重构的三元逻辑存储器(LIM)器件,该器件基于有机反双极晶体管,并将金浮栅集成到氧化铪(HfO 2)栅极绝缘体中。首先,由于HfO - 2栅极绝缘子的高介电常数,得到了一个输入和漏极电压极低(2 V)的标准三元逆变器。对于相应的输入逻辑状态(“0”、“1”、“2”),可以清楚地得到三种不同的输出逻辑状态(“2”、“1”、“0”)。然后,通过控制浮栅的空穴和电子注入过程,将电压转移曲线横向移动到1.8 V,获得三元非易失性存储器。该存储功能实现了多种可重构的三元逆变器操作。三个三元逆变器,即标准,负,和正三元逆变器,演示在一个单一的LIM设备。值得注意的是,这些逆变器操作是使用相同的输入电压执行的,然后通过调整浮栅的电荷条件(即空穴或电子)进行电重新配置。我们的发展似乎有希望执行多值内存计算,以超越现有的冯·诺伊曼系统的能力。
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引用次数: 0
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Advanced Electronic Materials
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