首页 > 最新文献
paperpass

Advanced Electronic Materials最新文献

英文 中文
A Full Physical Strategy for Electrical Contacts on Laser‐Induced Graphene (LIG) Electrodes 激光诱导石墨烯(LIG)电极电接触的完整物理策略
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-15 DOI: 10.1002/aelm.70576
Davide Arcoraci, Simone Martellone, Michele Miceli, Davide Molino, Luigi Ribotta, Giulia Mossotti, Alessio Testa, Valentina Bertana, Luciano Scaltrito, Andrea Lamberti
Laser‐induced graphene (LIG) has emerged as a highly promising material for energy storage devices due to its excellent electrical conductivity, high specific surface area, and compatibility with flexible substrates. Despite these advantages, one of the main challenges in implementing LIG‐based electrodes is achieving a stable and efficient electrical connection with metallic current collectors without compromising the intrinsic properties of the material. In this study, we investigate a combination of physical approaches to establish a reliable and robust electrical bond between LIG and metal current collectors while avoiding chemical treatments, conductive adhesives, or binders. Electrode fabrication is performed using physical vapor deposition (PVD) and laser processing techniques, which provide precise control over both metallic layer deposition and LIG formation. These methods enable straightforward customization of electrode architectures for applications, including symmetric and hybrid energy storage devices. Furthermore, fast and selective laser treatments are adopted to enhance the mechanical integrity and long‐term stability of the electrode interfaces. Our results demonstrate a contact resistance as low as 1.3 Ω at the LIG‐gold interface without the use of binders or additional conductive agents. The proposed fabrication strategy improves electrical performance while simplifying the overall manufacturing process. By minimizing complex chemical procedures, it enables scalability.
激光诱导石墨烯(LIG)由于其优异的导电性、高比表面积和与柔性衬底的相容性,已成为一种非常有前途的储能器件材料。尽管有这些优点,但实现基于LIG电极的主要挑战之一是在不影响材料固有特性的情况下实现与金属集流器的稳定高效的电连接。在这项研究中,我们研究了物理方法的组合,以在LIG和金属集流器之间建立可靠而坚固的电键,同时避免了化学处理、导电粘合剂或粘合剂。电极制造使用物理气相沉积(PVD)和激光加工技术,提供精确控制金属层沉积和LIG形成。这些方法可以直接定制应用的电极架构,包括对称和混合储能设备。此外,采用快速和选择性激光处理来提高电极界面的机械完整性和长期稳定性。我们的研究结果表明,在不使用粘合剂或其他导电剂的情况下,LIG - gold界面的接触电阻低至1.3 Ω。提出的制造策略在简化整个制造过程的同时提高了电气性能。通过最大限度地减少复杂的化学过程,它实现了可扩展性。
{"title":"A Full Physical Strategy for Electrical Contacts on Laser‐Induced Graphene (LIG) Electrodes","authors":"Davide Arcoraci, Simone Martellone, Michele Miceli, Davide Molino, Luigi Ribotta, Giulia Mossotti, Alessio Testa, Valentina Bertana, Luciano Scaltrito, Andrea Lamberti","doi":"10.1002/aelm.70576","DOIUrl":"https://doi.org/10.1002/aelm.70576","url":null,"abstract":"Laser‐induced graphene (LIG) has emerged as a highly promising material for energy storage devices due to its excellent electrical conductivity, high specific surface area, and compatibility with flexible substrates. Despite these advantages, one of the main challenges in implementing LIG‐based electrodes is achieving a stable and efficient electrical connection with metallic current collectors without compromising the intrinsic properties of the material. In this study, we investigate a combination of physical approaches to establish a reliable and robust electrical bond between LIG and metal current collectors while avoiding chemical treatments, conductive adhesives, or binders. Electrode fabrication is performed using physical vapor deposition (PVD) and laser processing techniques, which provide precise control over both metallic layer deposition and LIG formation. These methods enable straightforward customization of electrode architectures for applications, including symmetric and hybrid energy storage devices. Furthermore, fast and selective laser treatments are adopted to enhance the mechanical integrity and long‐term stability of the electrode interfaces. Our results demonstrate a contact resistance as low as 1.3 Ω at the LIG‐gold interface without the use of binders or additional conductive agents. The proposed fabrication strategy improves electrical performance while simplifying the overall manufacturing process. By minimizing complex chemical procedures, it enables scalability.","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"21 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148979608","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
Core and π‐Bridge Engineering to Deconstruct Y6‐Series into Modular Non‐Fused Acceptors: DFT‐Guided Structure‐Property Map for Organic Solar Cells 核心和π桥工程将Y6系列解构为模块化非熔接受体:有机太阳能电池的DFT引导结构-性质图
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-15 DOI: 10.1002/aelm.70572
Qurat ul Ain, Waqas Akram, Hasan Yaqoob, Munazza Shahid, Abdul Majid, Muhammad Altaf, Christian B. Nielsen, Raja Shahid Ashraf
Non‐fullerene acceptors have propelled organic solar cells beyond 20% efficiency, yet the fused Y‐series backbones enabling high performance impose synthetic complexity and limited modularity. In this theoretical study, we propose a backbone deconstruction strategy, converting the BTP‐4Cl acceptor into an A‐π‐A′‐π‐A type non‐fused architecture to establish atomistic structure‐property relationships for core and bridge engineering. Six acceptors (Q1‐Q6) were designed by tuning the π‐bridge from thiophene to thienothiophene and the central BTD core to dithiophene‐based DT‐BTD, conjugation‐extended 4T‐BTD, and thiazole‐enriched TZT‐BTD. Density Functional Theory calculations show that the designed acceptors retain efficient Y‐class electronic structures and narrow energy gaps, yielding Scharber‐estimated V OC of 1.01–1.17 V against PM6 donor. Designed acceptors exhibited broad near‐IR absorption with λ max of 642–751 nm and achieved dominant charge‐transfer character, reaching 84% ICT excitations compared to 53% for BTP‐4Cl. Notably, the designs maintained tight solid‐state packing with significantly reduced reorganization energies (0.132–0.164 eV), achieving up to a four‐fold enhancement in electron mobility (9.43 × 10 − 1 cm 2 V − 1 s − 1 ) over the benchmark BTP‐4Cl. Interfacial calculations further indicated markedly strengthened PM6:acceptor electronic couplings for robust charge separation and low recombination losses. Overall, this study demonstrates that non‐fused engineering successfully preserves Y‐series optoelectronics while improving intrinsic electron transport and charge separation for efficient organic photovoltaics.
非富勒烯受体已将有机太阳能电池的效率提高到20%以上,但Y系列主干网实现了高性能,却增加了合成的复杂性和有限的模块化。在这项理论研究中,我们提出了一种骨干解构策略,将BTP‐4Cl受体转化为a‐π‐a’‐π‐a型非融合结构,以建立原子结构-性质关系,用于核心和桥梁工程。通过调整从噻吩到噻吩的π桥和中央BTD核心到二噻吩基DT - BTD,共轭扩展4T - BTD和噻唑富集TZT - BTD,设计了六个受体(Q1 - Q6)。密度泛函理论计算表明,所设计的受体保持了高效的Y级电子结构和窄的能隙,相对于PM6供体,Scharber估计的V OC为1.01-1.17 V。设计的受体具有广泛的近红外吸收,λ max为642-751 nm,并具有优势电荷转移特性,达到84%的ICT激发,而BTP‐4Cl为53%。值得注意的是,这些设计保持了紧密的固态填充,重组能显著降低(0.132-0.164 eV),电子迁移率(9.43 × 10−1 cm 2 V−1 s−1)比基准BTP‐4Cl提高了四倍。界面计算进一步表明,明显加强PM6:受体电子耦合,以实现稳健的电荷分离和低复合损失。总的来说,这项研究表明,非熔融工程成功地保留了Y系列光电子器件,同时改善了高效有机光伏电池的内在电子传递和电荷分离。
{"title":"Core and π‐Bridge Engineering to Deconstruct Y6‐Series into Modular Non‐Fused Acceptors: DFT‐Guided Structure‐Property Map for Organic Solar Cells","authors":"Qurat ul Ain, Waqas Akram, Hasan Yaqoob, Munazza Shahid, Abdul Majid, Muhammad Altaf, Christian B. Nielsen, Raja Shahid Ashraf","doi":"10.1002/aelm.70572","DOIUrl":"https://doi.org/10.1002/aelm.70572","url":null,"abstract":"Non‐fullerene acceptors have propelled organic solar cells beyond 20% efficiency, yet the fused Y‐series backbones enabling high performance impose synthetic complexity and limited modularity. In this theoretical study, we propose a backbone deconstruction strategy, converting the BTP‐4Cl acceptor into an A‐π‐A′‐π‐A type non‐fused architecture to establish atomistic structure‐property relationships for core and bridge engineering. Six acceptors (Q1‐Q6) were designed by tuning the π‐bridge from thiophene to thienothiophene and the central BTD core to dithiophene‐based DT‐BTD, conjugation‐extended 4T‐BTD, and thiazole‐enriched TZT‐BTD. Density Functional Theory calculations show that the designed acceptors retain efficient Y‐class electronic structures and narrow energy gaps, yielding Scharber‐estimated V <jats:sub>OC</jats:sub> of 1.01–1.17 V against PM6 donor. Designed acceptors exhibited broad near‐IR absorption with λ <jats:sub>max</jats:sub> of 642–751 nm and achieved dominant charge‐transfer character, reaching 84% ICT excitations compared to 53% for BTP‐4Cl. Notably, the designs maintained tight solid‐state packing with significantly reduced reorganization energies (0.132–0.164 eV), achieving up to a four‐fold enhancement in electron mobility (9.43 × 10 <jats:sup>−</jats:sup> <jats:sup>1</jats:sup> cm <jats:sup>2</jats:sup> V <jats:sup>−</jats:sup> <jats:sup>1</jats:sup> s <jats:sup>−</jats:sup> <jats:sup>1</jats:sup> ) over the benchmark BTP‐4Cl. Interfacial calculations further indicated markedly strengthened PM6:acceptor electronic couplings for robust charge separation and low recombination losses. Overall, this study demonstrates that non‐fused engineering successfully preserves Y‐series optoelectronics while improving intrinsic electron transport and charge separation for efficient organic photovoltaics.","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"120 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148979606","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
AI‐Assisted Ultrasensitive Biosensing using Metal‐Electrolyte‐Metal‐Insulator‐Silicon Structure Based on Oxygen‐Tunable Iridium Oxide Nanonets for Lysyl‐Oxidase‐Like‐2 Breast Cancer Detection 基于氧可调氧化铱纳米网的金属-电解质-金属-绝缘体-硅结构的人工智能辅助超灵敏生物传感用于Lysyl -氧化酶- Like - 2乳腺癌检测
IF 6.2 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-15 DOI: 10.1002/aelm.70571
Chiao‐Fan Chiu, Pankaj Kumar, Long Nguyen Minh Le, Ping‐Hsuan Wu, Punnatorn Boonyoung, Shen Tingyang, Abhijit Aich, Yi‐Pin Chen, Shih‐Yin Huang, Siddheswar Maikap
Early detection of breast cancer metastasis is critical for improving survival rates, yet identifying specific biomarkers such as Lysyl‐Oxidase‐Like‐2 (LOXL2) at low concentrations remains challenging. A highly sensitive, label‐free sensor utilizing a Metal‐Electrolyte‐Metal‐Insulator‐Silicon (MEMIS) configuration based on oxygen‐controlled iridium oxide (IrO x ) nano‐nets is reported for LOXL2 detection. By optimizing the reactive sputtering oxygen content (50%) and film thickness (2 nm), the IrOx nano‐net structure achieves a super‐Nernstian pH sensitivity of 150.4 mV/pH with minimal drift (1.95 mV/h). This exceptional sensitivity is attributed to high porosity and abundant redox‐active sites of the crystalline nano‐nets, which facilitate volumetric potential accumulation and significantly enhance the Limit of Detection (LoD) to 0.05 nM. To address subtle signal variations often obscured by noise, a dual‐branch 1D Convolutional Neural Network (1D‐CNN) was integrated to simulate and analyze sensor performance. The Artificial Intelligence (AI) model successfully identifies characteristic sub‐threshold voltage shifts associated with low‐abundance biomarkers, achieving diagnostic accuracy of 94.8%. This MEMIS‐AI platform serves as a promising bridge toward future ultrasensitive clinical screening.
早期发现乳腺癌转移对于提高生存率至关重要,但在低浓度下识别特定的生物标志物,如赖氨酸氧化酶样2 (LOXL2),仍然具有挑战性。报道了一种基于氧控氧化铱(IrO x)纳米网络的金属-电解质-金属-绝缘体-硅(MEMIS)结构的高灵敏度、无标签传感器,用于LOXL2检测。通过优化反应溅射氧含量(50%)和膜厚度(2 nm), IrOx纳米网结构获得了150.4 mV/pH的超Nernstian pH灵敏度和最小漂移(1.95 mV/h)。这种特殊的灵敏度归因于晶体纳米网的高孔隙率和丰富的氧化还原活性位点,这有利于体积电位的积累,并显著提高了检测限(LoD)至0.05 nM。为了解决经常被噪声掩盖的细微信号变化,集成了双分支一维卷积神经网络(1D - CNN)来模拟和分析传感器性能。人工智能(AI)模型成功识别出与低丰度生物标志物相关的亚阈值电压偏移特征,诊断准确率达到94.8%。这个MEMIS - AI平台是未来超灵敏临床筛查的一个有希望的桥梁。
{"title":"AI‐Assisted Ultrasensitive Biosensing using Metal‐Electrolyte‐Metal‐Insulator‐Silicon Structure Based on Oxygen‐Tunable Iridium Oxide Nanonets for Lysyl‐Oxidase‐Like‐2 Breast Cancer Detection","authors":"Chiao‐Fan Chiu, Pankaj Kumar, Long Nguyen Minh Le, Ping‐Hsuan Wu, Punnatorn Boonyoung, Shen Tingyang, Abhijit Aich, Yi‐Pin Chen, Shih‐Yin Huang, Siddheswar Maikap","doi":"10.1002/aelm.70571","DOIUrl":"https://doi.org/10.1002/aelm.70571","url":null,"abstract":"Early detection of breast cancer metastasis is critical for improving survival rates, yet identifying specific biomarkers such as Lysyl‐Oxidase‐Like‐2 (LOXL2) at low concentrations remains challenging. A highly sensitive, label‐free sensor utilizing a Metal‐Electrolyte‐Metal‐Insulator‐Silicon (MEMIS) configuration based on oxygen‐controlled iridium oxide (IrO <jats:sub>x</jats:sub> ) nano‐nets is reported for LOXL2 detection. By optimizing the reactive sputtering oxygen content (50%) and film thickness (2 nm), the IrOx nano‐net structure achieves a super‐Nernstian pH sensitivity of 150.4 mV/pH with minimal drift (1.95 mV/h). This exceptional sensitivity is attributed to high porosity and abundant redox‐active sites of the crystalline nano‐nets, which facilitate volumetric potential accumulation and significantly enhance the Limit of Detection (LoD) to 0.05 nM. To address subtle signal variations often obscured by noise, a dual‐branch 1D Convolutional Neural Network (1D‐CNN) was integrated to simulate and analyze sensor performance. The Artificial Intelligence (AI) model successfully identifies characteristic sub‐threshold voltage shifts associated with low‐abundance biomarkers, achieving diagnostic accuracy of 94.8%. This MEMIS‐AI platform serves as a promising bridge toward future ultrasensitive clinical screening.","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"21 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148979609","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
Electrode-Engineered Dual-Mode Multifunctional Lead-Free Perovskite Optoelectronic Memristors for Neuromorphic Computing 用于神经形态计算的电极工程双模多功能无铅钙钛矿光电忆阻器
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-11 Epub Date: 2026-01-26 DOI: 10.1002/aelm.202500713
Michalis Loizos, Konstantinos Rogdakis, Konstantinos Chatzimanolis, Katerina Anagnostou, Emmanuel Kymakis

Memristive devices based on halide perovskites hold strong promise to provide energy-efficient systems for the Internet of Things (IoT); however, lead (Pb) element should be minimized or ideally replaced. Herein, we introduce a multifunctional device based on AgBiI4 Pb-free perovskite as the active layer in a normal n-i-p solar cell configuration that exhibitss multiple mode-dependent neuromorphic functions. Specifically, through electrode engineering, we show a selection between volatile or non-volatile memristive switching when the Au top electrode is replaced by Ag. The volatile device having an Au top electrode can be used for emulating threshold-dependent artificial neuron firing processes, while the non-volatile device with Ag pads can emulate numerous synaptic protocols (LTP/LTD, PPF, STDP, SRDP, LTM, STM). Both volatile (VTH = −0.86 V) and non-volatile modes possess switching low voltages <1 V, while the ON/OFF ratio of the non-volatile system is 104 with a cycling endurance of 103 cycles and state retention of 103 s. Further investigation reveals that electrode type affects the conduction mechanism, as ion charge trapping and detrapping govern threshold switching with activation energy EA ≈ 0.7 eV, while the formation/rupture of Ag filaments is responsible for non-volatile switching. The response in both modes of devices can be tuned by light, while associative learning by emulating Pavlovian learning is demonstrated. Finally, experimental non-volatile data were used for MNIST and Fashion-MNIST classification, achieving 97.11% and 87.56% accuracy, respectively. Our work provides insights into electrode-engineered mode control in lead-free perovskite systems capable for a concurrent energy harvesting (PCE ∼1%) toward self-powered systems for neuromorphic edge computing.

基于卤化物钙钛矿的记忆器件有望为物联网(IoT)提供节能系统;然而,铅(Pb)元素应尽量减少或理想的替代。在此,我们介绍了一种基于AgBiI4无铅钙钛矿作为正常n-i-p太阳能电池结构的活性层的多功能器件,该器件具有多种模式依赖的神经形态功能。具体来说,通过电极工程,我们展示了当Au顶部电极被Ag取代时,在挥发性或非挥发性记忆开关之间的选择。具有Au顶部电极的易失性器件可用于模拟阈值依赖性人工神经元放电过程,而具有Ag衬垫的非易失性器件可模拟多种突触协议(LTP/LTD, PPF, STDP, SRDP, LTM, STM)。易失性(VTH = - 0.86 V)和非易失性模式都具有低开关电压<;1 V,而非易失性系统的ON/OFF比为104,循环寿命为103次,状态保持为103 s。进一步的研究表明,电极类型影响传导机制,离子电荷捕获和去捕获决定了激活能EA≈0.7 eV的阈值开关,而银丝的形成/断裂负责非易失性开关。两种模式的设备的响应都可以通过光来调节,同时通过模仿巴甫洛夫学习来展示联想学习。最后,将实验非易失性数据用于MNIST和Fashion-MNIST分类,准确率分别达到97.11%和87.56%。我们的工作为无铅钙钛矿系统中的电极工程模式控制提供了见解,该系统能够同时收集能量(PCE ~ 1%),用于神经形态边缘计算的自供电系统。
{"title":"Electrode-Engineered Dual-Mode Multifunctional Lead-Free Perovskite Optoelectronic Memristors for Neuromorphic Computing","authors":"Michalis Loizos,&nbsp;Konstantinos Rogdakis,&nbsp;Konstantinos Chatzimanolis,&nbsp;Katerina Anagnostou,&nbsp;Emmanuel Kymakis","doi":"10.1002/aelm.202500713","DOIUrl":"10.1002/aelm.202500713","url":null,"abstract":"<p>Memristive devices based on halide perovskites hold strong promise to provide energy-efficient systems for the Internet of Things (IoT); however, lead (Pb) element should be minimized or ideally replaced. Herein, we introduce a multifunctional device based on AgBiI<sub>4</sub> Pb-free perovskite as the active layer in a normal n-i-p solar cell configuration that exhibitss multiple mode-dependent neuromorphic functions. Specifically, through electrode engineering, we show a selection between volatile or non-volatile memristive switching when the Au top electrode is replaced by Ag. The volatile device having an Au top electrode can be used for emulating threshold-dependent artificial neuron firing processes, while the non-volatile device with Ag pads can emulate numerous synaptic protocols (LTP/LTD, PPF, STDP, SRDP, LTM, STM). Both volatile (V<sub>TH</sub> = −0.86 V) and non-volatile modes possess switching low voltages &lt;1 V, while the ON/OFF ratio of the non-volatile system is 10<sup>4</sup> with a cycling endurance of 10<sup>3</sup> cycles and state retention of 10<sup>3</sup> s. Further investigation reveals that electrode type affects the conduction mechanism, as ion charge trapping and detrapping govern threshold switching with activation energy E<sub>A</sub> ≈ 0.7 eV, while the formation/rupture of Ag filaments is responsible for non-volatile switching. The response in both modes of devices can be tuned by light, while associative learning by emulating Pavlovian learning is demonstrated. Finally, experimental non-volatile data were used for MNIST and Fashion-MNIST classification, achieving 97.11% and 87.56% accuracy, respectively. Our work provides insights into electrode-engineered mode control in lead-free perovskite systems capable for a concurrent energy harvesting (PCE ∼1%) toward self-powered systems for neuromorphic edge computing.</p>","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"12 17","pages":""},"PeriodicalIF":5.9,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aelm.202500713","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146044873","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
RRAM Variability Harvesting for CIM-Integrated TRNG CIM集成TRNG的RRAM变异性采集
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-11 Epub Date: 2026-01-27 DOI: 10.1002/aelm.202500635
Ankit Bende, Gokulnath Rajendran, Regina Dittmann, Anupam Chattopadhyay, Vikas Rana

True random number generators (TRNGs) are essential for hardware security in edge AI systems, yet conventional designs often incur large analog overhead and limited throughput imposed by standalone macros. We present a Compute-in-Memory (CiM)-compatible TRNG that directly exploits the intrinsic stochasticity of TaOx-based 1T1R RRAM arrays, enabling entropy extraction within the memory fabric. Bit-rate is scaled by parallel column readout circuits consisting of a transimpedance amplifier (TIA) and an ADC. Our design achieves up to ∼270 Mbps throughput with TIA + 16-bit ADC per column. Furthermore, a lightweight shift-XOR post-processing stage permits reduction to 8-bit ADC resolution, lowering energy consumption to ∼51 pJ bit−1 without degrading randomness quality. Fully compatible with standard CiM read paths, the architecture introduces minimal hardware overhead and provides a scalable and energy-efficient foundation for secure random number generation in edge-AI applications.

真正的随机数生成器(trng)对于边缘人工智能系统的硬件安全性至关重要,但传统的设计通常会产生大量的模拟开销和由独立宏施加的有限吞吐量。我们提出了一种计算-内存(CiM)兼容的TRNG,它直接利用了基于TaO x的1T1R RRAM阵列的固有随机性,从而实现了内存结构内的熵提取。比特率由一个跨阻放大器(TIA)和一个ADC组成的并行列读出电路进行缩放。我们的设计通过TIA +每列16位ADC实现高达~ 270 Mbps的吞吐量。此外,轻量级的移异或后处理阶段允许将ADC分辨率降低到8位,在不降低随机性质量的情况下将能耗降低到51 pJ bit - 1。该架构与标准CiM读取路径完全兼容,引入了最小的硬件开销,并为边缘AI应用中的安全随机数生成提供了可扩展和节能的基础。
{"title":"RRAM Variability Harvesting for CIM-Integrated TRNG","authors":"Ankit Bende,&nbsp;Gokulnath Rajendran,&nbsp;Regina Dittmann,&nbsp;Anupam Chattopadhyay,&nbsp;Vikas Rana","doi":"10.1002/aelm.202500635","DOIUrl":"10.1002/aelm.202500635","url":null,"abstract":"<p>True random number generators (TRNGs) are essential for hardware security in edge AI systems, yet conventional designs often incur large analog overhead and limited throughput imposed by standalone macros. We present a Compute-in-Memory (CiM)-compatible TRNG that directly exploits the intrinsic stochasticity of TaO<sub>x</sub>-based 1T1R RRAM arrays, enabling entropy extraction within the memory fabric. Bit-rate is scaled by parallel column readout circuits consisting of a transimpedance amplifier (TIA) and an ADC. Our design achieves up to ∼270 Mbps throughput with TIA + 16-bit ADC per column. Furthermore, a lightweight shift-XOR post-processing stage permits reduction to 8-bit ADC resolution, lowering energy consumption to ∼51 pJ bit<sup>−1</sup> without degrading randomness quality. Fully compatible with standard CiM read paths, the architecture introduces minimal hardware overhead and provides a scalable and energy-efficient foundation for secure random number generation in edge-AI applications.</p>","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"12 17","pages":""},"PeriodicalIF":5.9,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aelm.202500635","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146056267","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Linear and Programmable Long-Term Plasticity in PECVD Amorphous SiC Memristors PECVD非晶SiC忆阻器的线性和可编程长期可塑性
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-11 Epub Date: 2026-07-28 DOI: 10.1002/aelm.70508
Qin Liu, Omesh Kapur, Bohao Ding, Fangnan Chen, Bingkai Ding, Ruomeng Huang, C. H. Kees de Groot

Amorphous silicon carbide (SiC) is a promising dielectric platform for memristive artificial synapses due to its high stability and back-end-of-line compatibility for CMOS integration. Here, we demonstrate stoichiometric PECVD-grown amorphous SiC memristors with Cu active electrodes, in which synaptic functionality is engineered through control of material composition. By tuning the SiC stoichiometry from Si-rich to near-stoichiometric, the bonding configuration is modified to suppress excessive Cu ion migration, enabling gradual and stable conductance evolution. The resulting devices exhibit highly linear and programmable long-term potentiation and depression, with a low nonlinearity of 0.08, uniform conductance updates, and minimal cycle-to-cycle variation. The synaptic behavior is further shown to be controllable through pulse programming, enabling tunable multilevel conductance states. Using experimentally extracted device characteristics, we implement both artificial neural networks and convolutional neural networks to evaluate system-level performance. The memristor-based networks achieve classification accuracies exceeding 95% on MNIST and 90% on CIFAR-10, while maintaining robust performance under conductance discretisation and cycle-to-cycle variation. These results demonstrate a materials-driven approach to achieving linear and controllable synaptic behavior, establishing PECVD amorphous SiC as a strong candidate for high-precision and scalable neuromorphic computing systems.

非晶碳化硅(SiC)由于其高稳定性和对CMOS集成的后端兼容性,是一种很有前途的记忆性人工突触介质平台。在这里,我们展示了化学计量PECVD生长的非晶SiC忆阻器与Cu有源电极,其中突触功能是通过控制材料组成来设计的。通过将碳化硅的化学计量从富硅调整到接近化学计量,可以修改键构型以抑制过量的Cu离子迁移,从而实现逐渐稳定的电导演化。所得到的器件表现出高度线性和可编程的长期增强和抑制,具有0.08的低非线性,均匀的电导更新和最小的周期变化。通过脉冲编程进一步证明突触行为是可控的,从而实现可调的多电平电导状态。利用实验提取的器件特性,我们实现了人工神经网络和卷积神经网络来评估系统级性能。基于忆阻器的网络在MNIST上的分类准确率超过95%,在CIFAR - 10上的分类准确率超过90%,同时在电导离散化和周期变化下保持稳健的性能。这些结果展示了一种材料驱动的方法来实现线性和可控的突触行为,建立了PECVD非晶SiC作为高精度和可扩展的神经形态计算系统的有力候选。
{"title":"Linear and Programmable Long-Term Plasticity in PECVD Amorphous SiC Memristors","authors":"Qin Liu,&nbsp;Omesh Kapur,&nbsp;Bohao Ding,&nbsp;Fangnan Chen,&nbsp;Bingkai Ding,&nbsp;Ruomeng Huang,&nbsp;C. H. Kees de Groot","doi":"10.1002/aelm.70508","DOIUrl":"10.1002/aelm.70508","url":null,"abstract":"<p>Amorphous silicon carbide (SiC) is a promising dielectric platform for memristive artificial synapses due to its high stability and back-end-of-line compatibility for CMOS integration. Here, we demonstrate stoichiometric PECVD-grown amorphous SiC memristors with Cu active electrodes, in which synaptic functionality is engineered through control of material composition. By tuning the SiC stoichiometry from Si-rich to near-stoichiometric, the bonding configuration is modified to suppress excessive Cu ion migration, enabling gradual and stable conductance evolution. The resulting devices exhibit highly linear and programmable long-term potentiation and depression, with a low nonlinearity of 0.08, uniform conductance updates, and minimal cycle-to-cycle variation. The synaptic behavior is further shown to be controllable through pulse programming, enabling tunable multilevel conductance states. Using experimentally extracted device characteristics, we implement both artificial neural networks and convolutional neural networks to evaluate system-level performance. The memristor-based networks achieve classification accuracies exceeding 95% on MNIST and 90% on CIFAR-10, while maintaining robust performance under conductance discretisation and cycle-to-cycle variation. These results demonstrate a materials-driven approach to achieving linear and controllable synaptic behavior, establishing PECVD amorphous SiC as a strong candidate for high-precision and scalable neuromorphic computing systems.</p>","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"12 17","pages":""},"PeriodicalIF":5.9,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aelm.70508","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148633895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Thermoelectric p-Type Iron-Based Ethylenetetrathiolate Coordination Polymers 热电p型铁基乙烯四硫酸盐配位聚合物
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-11 Epub Date: 2026-08-25 DOI: 10.1002/aelm.70547
Malar Auxilia Francis, Mari Heikkinen, Girish C. Tewari, Kristoffer Meinander, Johan Lindén, Maarit Karppinen

Here we demonstrate high room-temperature Seebeck coefficient of 95 µV K−1 in combination with ultralow thermal conductivity of 0.18 W m−1 K−1 for a novel bimetallic p-type semiconducting coordination polymer. We synthesize the (Fe, Cu) bimetallic coordination polymer together with the single-metal Cu and Fe counterparts using 1,3,4,6- tetrathiapentalene-2,5-dione (TPD) as the organic ligand. The resultant poly[metal-ethylenetetrathiolate] materials are characterized by XPS (X-ray photoelectron spectroscopy) and Mössbauer spectroscopy techniques for the copper and iron metal oxidation states and with PPMS (physical property measurement system) for electronic and thermal transport properties in the temperature range of 100–350 K. The heterobimetallic effect in poly[(Fe, Cu)-ETT] is best appreciated regarding the enhanced Seebeck coefficient. We foresee that the present p-type poly[(Fe, Cu)-ETT] thermoelectrics could be a promising counterpart for the previously more widely investigated n-type conducting polymers.

在这里,我们证明了一种新型双金属p型半导体配位聚合物的高室温塞贝克系数为95 μ V K−1,超低导热系数为0.18 W m−1 K−1。以1,3,4,6‐四thiapentalene‐2,5‐dione (TPD)为有机配体,合成了(Fe, Cu)双金属配位聚合物以及单金属Cu和Fe对应物。用XPS (X射线光电子能谱)和Mössbauer能谱技术对铜和铁金属的氧化态进行了表征,并用PPMS(物理性质测量系统)对100-350 K温度范围内的电子和热输运性质进行了表征。多[(Fe, Cu)‐ETT]中的杂双金属效应在塞贝克系数的增强方面得到了最好的评价。我们预见到,目前的p型聚[(Fe, Cu)‐ETT]热电材料可能是先前更广泛研究的n型导电聚合物的有希望的对立物。
{"title":"Thermoelectric p-Type Iron-Based Ethylenetetrathiolate Coordination Polymers","authors":"Malar Auxilia Francis,&nbsp;Mari Heikkinen,&nbsp;Girish C. Tewari,&nbsp;Kristoffer Meinander,&nbsp;Johan Lindén,&nbsp;Maarit Karppinen","doi":"10.1002/aelm.70547","DOIUrl":"10.1002/aelm.70547","url":null,"abstract":"<p>Here we demonstrate high room-temperature Seebeck coefficient of 95 µV K<sup>−1</sup> in combination with ultralow thermal conductivity of 0.18 W m<sup>−1</sup> K<sup>−1</sup> for a novel bimetallic p-type semiconducting coordination polymer. We synthesize the (Fe, Cu) bimetallic coordination polymer together with the single-metal Cu and Fe counterparts using 1,3,4,6- tetrathiapentalene-2,5-dione (TPD) as the organic ligand. The resultant poly[metal-ethylenetetrathiolate] materials are characterized by XPS (X-ray photoelectron spectroscopy) and Mössbauer spectroscopy techniques for the copper and iron metal oxidation states and with PPMS (physical property measurement system) for electronic and thermal transport properties in the temperature range of 100–350 K. The heterobimetallic effect in poly[(Fe, Cu)-ETT] is best appreciated regarding the enhanced Seebeck coefficient. We foresee that the present p-type poly[(Fe, Cu)-ETT] thermoelectrics could be a promising counterpart for the previously more widely investigated n-type conducting polymers.</p>","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"12 17","pages":""},"PeriodicalIF":5.9,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aelm.70547","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148836273","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Analog Weight Update Rule in Ferroelectric Hafnia, Using picoJoule Programming Pulses 基于皮焦耳编程脉冲的铁电Hafnia模拟权值更新规则
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-11 Epub Date: 2026-05-07 DOI: 10.1002/aelm.202500823
Alexandre Baigol, Nikhil Garg, Matteo Mazza, Yanming Zhang, Elisa Zaccaria, Wooseok Choi, Bert Jan Offrein, Laura Bégon-Lours

In an effort to compete with the brain's efficiency at processing information, neuromorphic hardware combines artificial synapses and neurons using mixed-signal circuits and emerging memories. In ferroelectric resistive weights, the strength of the synaptic connection between two neurons is stored in the device conductance. During learning, programming pulses are applied to the synaptic weight, which reconfigures the ferroelectric domains and adjusts the conductance. One strategy to lower the energy cost during the training phase is to lower the duration of the programming pulses. However, the latter cannot be shorter than the self-loading time of the resistive weights, limited by intrinsic parasitics in the circuits. In this work, ferroelectric resistive weights are fabricated using a process compatible with CMOS Back-End-Of-Line integration, based on hafnia/zirconia nanolaminates. By laterally scaling the device area under 100 � � � μ� � � � $umu!!$� m2, the self-loading time becomes sufficiently short to enable 20 ns programming, which corresponds to a maximum of 3 picoJoules per pulse. Further, in this work, the weight update rule with 20 ns pulses is experimentally measured not only for different amplitudes but also for different initial conductance states. We find that the final weight is determined by the pulse amplitude, independent of the initial weight value.

为了与大脑处理信息的效率相竞争,神经形态硬件结合了人工突触和神经元,使用混合信号电路和新兴记忆。在铁电电阻重量中,两个神经元之间突触连接的强度存储在器件电导中。在学习过程中,将编程脉冲应用于突触权,重新配置铁电畴并调整电导。在训练阶段降低能量消耗的一种策略是降低编程脉冲的持续时间。然而,后者不能短于电阻权重的自加载时间,受限于电路中的固有寄生。在这项工作中,铁电电阻砝码是基于半氧化锆/氧化锆纳米层合材料,使用与CMOS后端线集成兼容的工艺制造的。通过横向缩放器件面积到100 m2以下,自加载时间变得足够短,可以实现20 ns编程,这相当于每个脉冲最大3皮焦耳。此外,本文还实验测量了20 ns脉冲在不同振幅和不同初始电导状态下的权值更新规律。我们发现最终权值是由脉冲幅度决定的,与初始权值无关。
{"title":"Analog Weight Update Rule in Ferroelectric Hafnia, Using picoJoule Programming Pulses","authors":"Alexandre Baigol,&nbsp;Nikhil Garg,&nbsp;Matteo Mazza,&nbsp;Yanming Zhang,&nbsp;Elisa Zaccaria,&nbsp;Wooseok Choi,&nbsp;Bert Jan Offrein,&nbsp;Laura Bégon-Lours","doi":"10.1002/aelm.202500823","DOIUrl":"10.1002/aelm.202500823","url":null,"abstract":"<p>In an effort to compete with the brain's efficiency at processing information, neuromorphic hardware combines artificial synapses and neurons using mixed-signal circuits and emerging memories. In ferroelectric resistive weights, the strength of the synaptic connection between two neurons is stored in the device conductance. During learning, programming pulses are applied to the synaptic weight, which reconfigures the ferroelectric domains and adjusts the conductance. One strategy to lower the energy cost during the training phase is to lower the duration of the programming pulses. However, the latter cannot be shorter than the self-loading time of the resistive weights, limited by intrinsic parasitics in the circuits. In this work, ferroelectric resistive weights are fabricated using a process compatible with CMOS Back-End-Of-Line integration, based on hafnia/zirconia nanolaminates. By laterally scaling the device area under 100 <span></span><math>\u0000 <semantics>\u0000 <mrow>\u0000 <mi>μ</mi>\u0000 <mspace></mspace>\u0000 <mspace></mspace>\u0000 </mrow>\u0000 <annotation>$umu!!$</annotation>\u0000 </semantics></math> m<sup>2</sup>, the self-loading time becomes sufficiently short to enable 20 ns programming, which corresponds to a maximum of 3 picoJoules per pulse. Further, in this work, the weight update rule with 20 ns pulses is experimentally measured not only for different amplitudes but also for different initial conductance states. We find that the final weight is determined by the pulse amplitude, independent of the initial weight value.</p>","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"12 17","pages":""},"PeriodicalIF":5.9,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aelm.202500823","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148287497","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Probing of Single-Interface Dzyaloshinskii-Moriya Interaction 单界面Dzyaloshinskii - Moriya相互作用的探测
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-11 Epub Date: 2026-08-17 DOI: 10.1002/aelm.70537
Ji-Sung Yu, Seong-Hyub Lee, Minhwan Kim, Dae-Yun Kim, Gunn-Hee Han, Wooyoung Shim, Jiho Shin, Yohan Mok, Jaehun Cho, Duck-Ho Kim, Sug-Bong Choe

The interfacial Dzyaloshinskii-Moriya interaction (DMI) is a fundamental antisymmetric exchange interaction that favors nonlinear spin orders and emerges prominently at interfaces in ultrathin magnetic films. The lack of single-interface resolution obscures both the magnitude and sign of the DMI at the interface of interest, and remains a challenge. Herein, we report the probing of a Pt/Co single-interface DMI under isolated interface conditions. Uncapped Co films on Pt were investigated in a vacuum using a magneto-optical Kerr microscope to observe the magnetic domains. The single-interface DMI is clearly revealed by the asymmetric domain-wall speed measurements. By resolving the Pt/Co single-interface DMI with systematic thickness control at a subatomic level, we confirm that subtle changes can be captured at the interface. This method offers a powerful tool for probing diverse interface-specific properties and is expected to advance the understanding of interface-driven physics with broad implications for chiral spin-orbitronics.

界面Dzyaloshinskii - Moriya相互作用(DMI)是一种基本的反对称交换相互作用,有利于非线性自旋顺序,并在超薄磁薄膜的界面中突出出现。单界面分辨率的缺乏模糊了感兴趣界面上DMI的大小和符号,这仍然是一个挑战。本文报道了在隔离界面条件下探测Pt/Co单界面DMI的方法。在真空条件下,利用磁光克尔显微镜观察了Pt上未封盖Co膜的磁畴。非对称畴壁速度测量清楚地揭示了单界面DMI。通过在亚原子水平上对Pt/Co单界面DMI进行系统厚度控制,我们证实了在界面上可以捕捉到细微的变化。该方法为探测不同的界面特性提供了一个强大的工具,并有望推进对界面驱动物理学的理解,对手性自旋轨道电子学具有广泛的影响。
{"title":"Probing of Single-Interface Dzyaloshinskii-Moriya Interaction","authors":"Ji-Sung Yu,&nbsp;Seong-Hyub Lee,&nbsp;Minhwan Kim,&nbsp;Dae-Yun Kim,&nbsp;Gunn-Hee Han,&nbsp;Wooyoung Shim,&nbsp;Jiho Shin,&nbsp;Yohan Mok,&nbsp;Jaehun Cho,&nbsp;Duck-Ho Kim,&nbsp;Sug-Bong Choe","doi":"10.1002/aelm.70537","DOIUrl":"10.1002/aelm.70537","url":null,"abstract":"<p>The interfacial Dzyaloshinskii-Moriya interaction (DMI) is a fundamental antisymmetric exchange interaction that favors nonlinear spin orders and emerges prominently at interfaces in ultrathin magnetic films. The lack of single-interface resolution obscures both the magnitude and sign of the DMI at the interface of interest, and remains a challenge. Herein, we report the probing of a Pt/Co single-interface DMI under isolated interface conditions. Uncapped Co films on Pt were investigated in a vacuum using a magneto-optical Kerr microscope to observe the magnetic domains. The single-interface DMI is clearly revealed by the asymmetric domain-wall speed measurements. By resolving the Pt/Co single-interface DMI with systematic thickness control at a subatomic level, we confirm that subtle changes can be captured at the interface. This method offers a powerful tool for probing diverse interface-specific properties and is expected to advance the understanding of interface-driven physics with broad implications for chiral spin-orbitronics.</p>","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"12 17","pages":""},"PeriodicalIF":5.9,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aelm.70537","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148754527","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Neuromorphic Deep-Ultraviolet Signal Processing Using a-Ga2O3 基于a - ga2o3的神经形态深紫外信号处理
IF 5.9 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-11 Epub Date: 2026-08-20 DOI: 10.1002/aelm.70542
Sidhant Sharma, Arthur Robert, Florian Wilke, Martin W. Allen, Valentina Baccetti, Jim G. Partridge, Hiep N. Tran

Neuromorphic signal processing has been performed by lateral metal-semiconductor-metal photodetectors supported on wide-bandgap thin-film amorphous gallium oxide (a-Ga2O3). Paired pulse facilitation (PPF) observed in the photocurrents of the devices was attributed to charge trapping and de-trapping in the a-Ga2O3 and depended systematically on the amplitude, duration, and interval of the pulsed ultraviolet-C (UVC) input. Four-bit UVC binary pulse sequences of optimized power were input to the device, and these produced separable electrical output currents (conductance states), measured after the pulse sequences. A simple resistor-capacitor (RC) equivalent circuit model replicated the neuromorphic device responses, and this model was used with and incorporated into single- and multi-node reservoir computers. Classification of electrocardiograms (ECGs) was performed in simulations using an RC model whose parameters were extracted from and validated against measured device responses. The single-node reservoir with virtual nodes achieved limited accuracy in classification depending on the heartbeat type, while the composite multi-node reservoir (consisting of eight RC sub-reservoirs with different time constants) exhibited significantly improved classification capability, achieving an average accuracy of ∼95%. These results highlight the potential of the a-Ga2O3 detectors as artificial synapses for neuromorphic signal processing and temporal pattern recognition.

神经形态信号处理是由横向金属-半导体-金属光电探测器进行的,该探测器由宽禁带薄膜非晶氧化镓(a - ga2o3)支撑。在器件的光电流中观察到的成对脉冲促进作用(PPF)归因于a - ga2o3中的电荷捕获和脱捕获,并且系统地取决于脉冲紫外- C (UVC)输入的振幅、持续时间和间隔。将优化功率的四比特UVC二进制脉冲序列输入到器件中,这些脉冲序列产生可分离的输出电流(电导状态),在脉冲序列后测量。一个简单的电阻-电容(RC)等效电路模型复制了神经形态器件的响应,并将该模型与单节点和多节点存储计算机结合使用。使用RC模型进行心电图(ECGs)的分类,该模型的参数是从测量的设备响应中提取并验证的。具有虚拟节点的单节点储层根据心跳类型的分类精度有限,而复合多节点储层(由8个具有不同时间常数的RC子储层组成)的分类能力显著提高,平均准确率达到约95%。这些结果突出了a - ga2o3探测器作为神经形态信号处理和时间模式识别的人工突触的潜力。
{"title":"Neuromorphic Deep-Ultraviolet Signal Processing Using a-Ga2O3","authors":"Sidhant Sharma,&nbsp;Arthur Robert,&nbsp;Florian Wilke,&nbsp;Martin W. Allen,&nbsp;Valentina Baccetti,&nbsp;Jim G. Partridge,&nbsp;Hiep N. Tran","doi":"10.1002/aelm.70542","DOIUrl":"10.1002/aelm.70542","url":null,"abstract":"<p>Neuromorphic signal processing has been performed by lateral metal-semiconductor-metal photodetectors supported on wide-bandgap thin-film amorphous gallium oxide (a-Ga<sub>2</sub>O<sub>3</sub>). Paired pulse facilitation (PPF) observed in the photocurrents of the devices was attributed to charge trapping and de-trapping in the a-Ga<sub>2</sub>O<sub>3</sub> and depended systematically on the amplitude, duration, and interval of the pulsed ultraviolet-C (UVC) input. Four-bit UVC binary pulse sequences of optimized power were input to the device, and these produced separable electrical output currents (conductance states), measured after the pulse sequences. A simple resistor-capacitor (RC) equivalent circuit model replicated the neuromorphic device responses, and this model was used with and incorporated into single- and multi-node reservoir computers. Classification of electrocardiograms (ECGs) was performed in simulations using an RC model whose parameters were extracted from and validated against measured device responses. The single-node reservoir with virtual nodes achieved limited accuracy in classification depending on the heartbeat type, while the composite multi-node reservoir (consisting of eight RC sub-reservoirs with different time constants) exhibited significantly improved classification capability, achieving an average accuracy of ∼95%. These results highlight the potential of the a-Ga<sub>2</sub>O<sub>3</sub> detectors as artificial synapses for neuromorphic signal processing and temporal pattern recognition.</p>","PeriodicalId":110,"journal":{"name":"Advanced Electronic Materials","volume":"12 17","pages":""},"PeriodicalIF":5.9,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aelm.70542","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148768827","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
期刊
Advanced Electronic Materials
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
﹀
mjeditor
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1