首页 > 最新文献

Nano-Micro Letters最新文献

英文 中文
Polyhydroxy Hydrogel Electrolyte with In Situ Tuned Interface Chemistry for Ultra-Stable Biosensing-Compatible Zinc Batteries 超稳定生物传感兼容锌电池用原位调谐界面化学多羟基水凝胶电解质。
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-26 DOI: 10.1007/s40820-025-02061-z
Fengjiao Guo, Chunjiang Jin, Hongyu Mi, Ziqiang Liu, Bo Xu, Wenhan Jia, Guozhao Fang, Jieshan Qiu

Highlights

  • Polyhydroxy hydrogel electrolyte enables in situ dual regulations of Zn-electrolyte interfacial chemistry and bulk electrolyte properties.

  • Reversible Zn anodes with exceptional cycling stability and perfect coulombic efficiency are achieved.

  • A self-powered biosensing platform that integrates Zn//I2 batteries with hydrogel sensor achieves real-time physiological monitoring.

水锌电池(ZBs)是一种有前途的可持续和安全的储能技术,但其广泛应用受到锌阳极持续界面不稳定的阻碍。本研究报道了一种具有原位调节界面化学的多羟基水凝胶电解质(PASHE),适用于生物传感相容zb。PASHE中富含羟基的l-山梨糖通过原位策略受益于良好的界面整合,建立了动力学上有利的Zn2+运输途径,调节界面离子吸附层次,协同均匀离子分布,促进优先结晶取向。此外,PASHE还通过界面优先吸附、富氧固体电解质界面相演化和Zn2+溶剂化鞘层重构构建了低水活度的微环境。这些效应实现了Zn(002)织体电沉积和抑制副反应,实现了无枝晶的Zn电镀/溶出,具有优异的稳定性(在Zn//Zn电池中3300小时)和近乎完美的可逆性(在Zn//Cu电池中1200次循环的平均库仑效率为99.6%)。该策略在柔性Zn/ I2电池(循环9000次后保持94.9%)和Zn离子混合电容器(循环43000次后保持98.0%)中提供了前所未有的可循环性。值得注意的是,我们展示了一个集成的生物传感平台,该平台将基于pashe的生物传感器与级联Zn//I2电池耦合,实现了生理信号和生物力学运动的实时监测。本研究提出了原位方法和功能添加剂的双重策略来设计水凝胶电解质,将高性能zb与下一代生物传感技术连接起来。
{"title":"Polyhydroxy Hydrogel Electrolyte with In Situ Tuned Interface Chemistry for Ultra-Stable Biosensing-Compatible Zinc Batteries","authors":"Fengjiao Guo,&nbsp;Chunjiang Jin,&nbsp;Hongyu Mi,&nbsp;Ziqiang Liu,&nbsp;Bo Xu,&nbsp;Wenhan Jia,&nbsp;Guozhao Fang,&nbsp;Jieshan Qiu","doi":"10.1007/s40820-025-02061-z","DOIUrl":"10.1007/s40820-025-02061-z","url":null,"abstract":"<div><h2>Highlights</h2><div>\u0000 \u0000 <ul>\u0000 <li>\u0000 <p>Polyhydroxy hydrogel electrolyte enables in situ dual regulations of Zn-electrolyte interfacial chemistry and bulk electrolyte properties.</p>\u0000 </li>\u0000 <li>\u0000 <p>Reversible Zn anodes with exceptional cycling stability and perfect coulombic efficiency are achieved.</p>\u0000 </li>\u0000 <li>\u0000 <p>A self-powered biosensing platform that integrates Zn//I<sub>2</sub> batteries with hydrogel sensor achieves real-time physiological monitoring.</p>\u0000 </li>\u0000 </ul>\u0000 </div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-025-02061-z.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146044604","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Integrated Performance Metrics of Porous Carbon Toward Practical Supercapacitor Devices 面向实用超级电容器器件的多孔碳综合性能指标。
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-26 DOI: 10.1007/s40820-026-02069-z
Yuting Song, Sicheng Fan, Zerui Yan, Dafu Tang, Xiang Gao, Jiawei Guo, Yunlong Zhao, Qiulong Wei

The scientific communities in both academia and industry are devoted to increasing energy density of supercapacitor devices, including investigating the relationship between carbon structure and capacitance of various activated carbon (AC) materials. However, most reported capacitance values are measured solely at the material level, which are difficult to directly translate into achievable energy densities for practical supercapacitor devices. In this work, we assemble supercapacitor pouch cells to reveal the insight relationships between the capacitance and porosity of AC materials and the optimal amount of electrolyte at the device level. Concurrently, a guidance on the required amount of electrolyte is provided, indicating that both the specific capacitance and porosity of AC materials collectively determine the energy density of a practical device (Edevice). Furthermore, we develop a computational E-tool for directly predicting Edevice at an early stage of material-level electrochemical testing. Finally, we propose a new descriptor (η) that incorporates both the capacitance and porosity parameters of AC materials, which displays a linear relationship with Edevice. This study provides a reliable E-tool and η for accelerating the development of advanced charge storage mechanisms and carbon materials for practical supercapacitor devices.

学术界和工业界都致力于提高超级电容器器件的能量密度,包括研究各种活性炭(AC)材料的碳结构与电容之间的关系。然而,大多数报道的电容值仅在材料水平上测量,这很难直接转化为实际超级电容器器件可实现的能量密度。在这项工作中,我们组装了超级电容器袋电池,以揭示交流材料的电容和孔隙率与器件级最佳电解质量之间的关系。同时,提供了所需电解质量的指导,表明交流材料的比电容和孔隙率共同决定了实际器件(Edevice)的能量密度。此外,我们开发了一个计算e -工具,用于在材料级电化学测试的早期阶段直接预测e - device。最后,我们提出了一个新的描述符(η),它包含了交流材料的电容和孔隙率参数,与Edevice呈线性关系。该研究为加速先进电荷存储机制和用于实用超级电容器器件的碳材料的开发提供了可靠的e -工具和η。
{"title":"Integrated Performance Metrics of Porous Carbon Toward Practical Supercapacitor Devices","authors":"Yuting Song,&nbsp;Sicheng Fan,&nbsp;Zerui Yan,&nbsp;Dafu Tang,&nbsp;Xiang Gao,&nbsp;Jiawei Guo,&nbsp;Yunlong Zhao,&nbsp;Qiulong Wei","doi":"10.1007/s40820-026-02069-z","DOIUrl":"10.1007/s40820-026-02069-z","url":null,"abstract":"<div><p>The scientific communities in both academia and industry are devoted to increasing energy density of supercapacitor devices, including investigating the relationship between carbon structure and capacitance of various activated carbon (AC) materials. However, most reported capacitance values are measured solely at the material level, which are difficult to directly translate into achievable energy densities for practical supercapacitor devices. In this work, we assemble supercapacitor pouch cells to reveal the insight relationships between the capacitance and porosity of AC materials and the optimal amount of electrolyte at the device level. Concurrently, a guidance on the required amount of electrolyte is provided, indicating that both the specific capacitance and porosity of AC materials collectively determine the energy density of a practical device (<i>E</i><sub>device</sub>). Furthermore, we develop a computational <i>E</i>-tool for directly predicting <i>E</i><sub>device</sub> at an early stage of material-level electrochemical testing. Finally, we propose a new descriptor (η) that incorporates both the capacitance and porosity parameters of AC materials, which displays a linear relationship with <i>E</i><sub>device</sub>. This study provides a reliable <i>E</i>-tool and η for accelerating the development of advanced charge storage mechanisms and carbon materials for practical supercapacitor devices.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-026-02069-z.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146044606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Microenvironment-Engineered Biocatalytic Metal–Organic Framework Nanomotors for Selective and Transformative Water Decontamination 微环境工程生物催化金属-有机框架纳米马达用于选择性和变革性水净化。
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-26 DOI: 10.1007/s40820-025-02064-w
Shu Xu, Jueyi Xue, Linyun Bao, Joel Yong, Ying Cao, Jun Ma, Kang Liang

Highlights

  • Biocatalytic metal–organic framework nanomotors were engineered with tunable microenvironment through a synergistic etching and surface engineering strategy.

  • Enhanced catalytic efficiency and selectivity for dye decontamination were achieved through charge-based enrichment and nanoconfinement effects.

  • Exceptional performance in water remediation of emerging contaminants, e.g., ~ 98% bisphenol A removal, in 2 min was achieved via enzymatic transformation into recoverable products.

催化动力微/纳米马达已成为传统催化剂在水修复中有效去除环境污染物的有力替代品。我们开发了一种新型的生物催化纳米马达系统,通过将过氧化氢酶和过氧化物酶封装到金属有机框架(MOFs)中,显示出卓越的速度和促进运动诱导的对流和传质。利用单宁酸(TA)的协同结构蚀刻和表面工程策略,我们创建了具有电荷选择和纳米限制特性的MOF框架的定制微环境。实验和模拟结果表明,微环境调节能与包封酶协同作用,显著提高了MOF基质去除带电荷污染物的效率和选择性。TA的表面工程通过调节MOF壳的表面电荷来选择性地预先浓缩目标污染物,而蚀刻诱导的空隙有助于快速将质量传递到酶活性位点。最后,我们还验证了这些纳米马达在通过酶介导的聚合途径将污染物从水相转化为聚合物产物中的适用性。这种生物催化纳米马达系统为减少碳排放和从新出现的污染物中回收化学能提供了一种有前途的水修复范例。
{"title":"Microenvironment-Engineered Biocatalytic Metal–Organic Framework Nanomotors for Selective and Transformative Water Decontamination","authors":"Shu Xu,&nbsp;Jueyi Xue,&nbsp;Linyun Bao,&nbsp;Joel Yong,&nbsp;Ying Cao,&nbsp;Jun Ma,&nbsp;Kang Liang","doi":"10.1007/s40820-025-02064-w","DOIUrl":"10.1007/s40820-025-02064-w","url":null,"abstract":"<div><h2>Highlights</h2><div>\u0000 \u0000 \u0000<ul>\u0000 <li>\u0000 <p>Biocatalytic metal–organic framework nanomotors were engineered with tunable microenvironment through a synergistic etching and surface engineering strategy.</p>\u0000 </li>\u0000 <li>\u0000 <p>Enhanced catalytic efficiency and selectivity for dye decontamination were achieved through charge-based enrichment and nanoconfinement effects.</p>\u0000 </li>\u0000 <li>\u0000 <p>Exceptional performance in water remediation of emerging contaminants, e.g., ~ 98% bisphenol A removal, in 2 min was achieved via enzymatic transformation into recoverable products.</p>\u0000 </li>\u0000 </ul>\u0000 </div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-025-02064-w.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146044600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unlocking Superior Stability in High-Salinity Oxygen Evolution Reaction: A Ru Stabilized NiFeOOH/Ni Anode with over 2000 h Durability 在高盐度析氧反应中解锁优越的稳定性:Ru稳定的NiFeOOH/Ni阳极具有超过2000小时的耐久性
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-26 DOI: 10.1007/s40820-026-02072-4
Jin He, Haoyun Sheng, Yichao Lin, Bingqi Gong, Yayun Zhao, Ziqi Tian, Liang Chen

Highlights

  • A dual-function stabilizing agent in NiFe-based anodes is proposed.

  • Ru incorporation promotes the formation of a protective surface layer enriched with Ru atoms, along with a denser NiFeOOH catalyst structure.

  • RuSA-NiFeOOH/Ni anode exhibits exceptional operational stability over 2000 h at an industrial current density of 0.5 A cm−2 in a chloride-enriched alkaline medium.

提出了一种用于镍铁基阳极的双功能稳定剂。Ru的掺入促进了富含Ru原子的保护表面层的形成,以及更致密的NiFeOOH催化剂结构。RuSA-NiFeOOH/Ni阳极在富含氯化物的碱性介质中,在工业电流密度为0.5 A cm - 2的情况下,在2000小时内表现出优异的运行稳定性。
{"title":"Unlocking Superior Stability in High-Salinity Oxygen Evolution Reaction: A Ru Stabilized NiFeOOH/Ni Anode with over 2000 h Durability","authors":"Jin He,&nbsp;Haoyun Sheng,&nbsp;Yichao Lin,&nbsp;Bingqi Gong,&nbsp;Yayun Zhao,&nbsp;Ziqi Tian,&nbsp;Liang Chen","doi":"10.1007/s40820-026-02072-4","DOIUrl":"10.1007/s40820-026-02072-4","url":null,"abstract":"<div><h2>Highlights</h2><div>\u0000 \u0000 <ul>\u0000 <li>\u0000 <p>A dual-function stabilizing agent in NiFe-based anodes is proposed.</p>\u0000 </li>\u0000 <li>\u0000 <p>Ru incorporation promotes the formation of a protective surface layer enriched with Ru atoms, along with a denser NiFeOOH catalyst structure.</p>\u0000 </li>\u0000 <li>\u0000 <p>Ru<sub>SA</sub>-NiFeOOH/Ni anode exhibits exceptional operational stability over 2000 h at an industrial current density of 0.5 A cm<sup>−2</sup> in a chloride-enriched alkaline medium.</p>\u0000 </li>\u0000 </ul>\u0000 </div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-026-02072-4.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146048635","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Flexible Polymer-Based Electronics for Human Health Monitoring: A Safety-Level-Oriented Review of Materials and Applications 用于人体健康监测的柔性聚合物电子器件:材料和应用的安全级综述。
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-21 DOI: 10.1007/s40820-025-02059-7
Dan Xu, Yi Yang, Keiji Numata, Bo Pang

Health monitoring is becoming increasingly critical for disease prevention, early diagnosis, and high-quality living. Polymeric materials, with their mechanical flexibility, biocompatibility, and tunable biochemical properties, offer unique advantages for creating next-generation personalized devices. In recent years, flexible polymer-based platforms have shown remarkable potential to capture diverse physiological signals in both daily and clinical contexts, including electrophysiological, biochemical, mechanical, and thermal indicators. In this review, we introduce a safety-level-oriented framework to evaluate material and device strategies for health monitoring, spanning the continuum from noninvasive wearables to deeply embedded implants. Physiological signals are systematically classified by use case, and application-specific requirements such as stability, comfort, and long-term compatibility are highlighted as critical factors guiding the selection of polymers, interfacial designs, and device architectures. Special emphasis is placed on mapping material types—including hydrogels, elastomers, and conductive composites—to their most suitable applications. Finally, we propose design principles for developing safe, functional, and adaptive polymer-based systems, aiming at reliable integration with the human body and enabling personalized, preventive healthcare.

健康监测对于疾病预防、早期诊断和高质量生活变得越来越重要。聚合物材料具有机械灵活性、生物相容性和可调生化特性,为制造下一代个性化设备提供了独特的优势。近年来,基于柔性聚合物的平台显示出在日常和临床环境中捕获各种生理信号的巨大潜力,包括电生理、生化、机械和热指标。在这篇综述中,我们介绍了一个以安全级别为导向的框架来评估健康监测的材料和设备策略,涵盖了从无创可穿戴设备到深度嵌入植入物的连续体。生理信号按用例系统分类,特定应用要求如稳定性、舒适性和长期兼容性被强调为指导聚合物选择、接口设计和设备架构的关键因素。特别强调的是映射材料类型-包括水凝胶,弹性体和导电复合材料-到他们最合适的应用。最后,我们提出了开发安全、功能性和适应性聚合物系统的设计原则,旨在与人体可靠地集成,实现个性化的预防性医疗保健。
{"title":"Flexible Polymer-Based Electronics for Human Health Monitoring: A Safety-Level-Oriented Review of Materials and Applications","authors":"Dan Xu,&nbsp;Yi Yang,&nbsp;Keiji Numata,&nbsp;Bo Pang","doi":"10.1007/s40820-025-02059-7","DOIUrl":"10.1007/s40820-025-02059-7","url":null,"abstract":"<div><p>Health monitoring is becoming increasingly critical for disease prevention, early diagnosis, and high-quality living. Polymeric materials, with their mechanical flexibility, biocompatibility, and tunable biochemical properties, offer unique advantages for creating next-generation personalized devices. In recent years, flexible polymer-based platforms have shown remarkable potential to capture diverse physiological signals in both daily and clinical contexts, including electrophysiological, biochemical, mechanical, and thermal indicators. In this review, we introduce a safety-level-oriented framework to evaluate material and device strategies for health monitoring, spanning the continuum from noninvasive wearables to deeply embedded implants. Physiological signals are systematically classified by use case, and application-specific requirements such as stability, comfort, and long-term compatibility are highlighted as critical factors guiding the selection of polymers, interfacial designs, and device architectures. Special emphasis is placed on mapping material types—including hydrogels, elastomers, and conductive composites—to their most suitable applications. Finally, we propose design principles for developing safe, functional, and adaptive polymer-based systems, aiming at reliable integration with the human body and enabling personalized, preventive healthcare.</p>\u0000<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-025-02059-7.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146005432","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Entropy-Driven Cellulosic Elastomer Self-Assembly for Mechanical Energy Harvesting and Self-Powered Sensing 用于机械能量收集和自供电传感的熵驱动纤维素弹性体自组装。
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-21 DOI: 10.1007/s40820-025-02054-y
Pinle Zhang, Yingping He, Huancheng Huang, Neng Xiong, Xinyue Nong, Xinke Yu, Shuangfei Wang, Xinliang Liu

Highlights

  • It systematically discusses the contribution of entropy-driven approaches to the design of self-assembled structures and performance regulation in cellulosic elastomers.

  • This review systematically examines design strategies for ordered self-assembled structures in cellulosic elastomers and investigates their structure-property relationships.

  • It presents a comprehensive review of performance design strategies for self-assembled cellulosic elastomers across mechanical and electrical domains, focusing on electromechanical conversion and self-powered sensing applications.

柔性电子技术的飞速发展对弹性材料的结构设计和性能调节提出了更高的要求。纤维素弹性体具有生物可降解性、可再生性和可调性,是理想的候选材料。熵驱动的自组装促进有序结构的自发形成,是优化纤维素弹性体性能的重要途径。然而,纤维素弹性体的自组装有序结构与其力学和电学性能之间的结构-性能关系尚未得到充分的研究。它阻碍了它们在电子设备中的应用。本文从熵驱动的角度系统地综述了自组装纤维素弹性体的结构-性能调控机制。阐述了机械能量收集和自供电传感的应用原理和性能优化策略,同时探讨了性能提升的挑战和前景。该工作为自组装纤维素弹性体在能源装置领域的发展提供了参考。
{"title":"Entropy-Driven Cellulosic Elastomer Self-Assembly for Mechanical Energy Harvesting and Self-Powered Sensing","authors":"Pinle Zhang,&nbsp;Yingping He,&nbsp;Huancheng Huang,&nbsp;Neng Xiong,&nbsp;Xinyue Nong,&nbsp;Xinke Yu,&nbsp;Shuangfei Wang,&nbsp;Xinliang Liu","doi":"10.1007/s40820-025-02054-y","DOIUrl":"10.1007/s40820-025-02054-y","url":null,"abstract":"<div><h2>Highlights</h2><div>\u0000 \u0000 <ul>\u0000 <li>\u0000 <p>It systematically discusses the contribution of entropy-driven approaches to the design of self-assembled structures and performance regulation in cellulosic elastomers.</p>\u0000 </li>\u0000 <li>\u0000 <p>This review systematically examines design strategies for ordered self-assembled structures in cellulosic elastomers and investigates their structure-property relationships.</p>\u0000 </li>\u0000 <li>\u0000 <p>It presents a comprehensive review of performance design strategies for self-assembled cellulosic elastomers across mechanical and electrical domains, focusing on electromechanical conversion and self-powered sensing applications.</p>\u0000 </li>\u0000 </ul>\u0000 </div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-025-02054-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146005429","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Temperature-Dependent Infrared Engineering for Extreme Environments: All-Dielectric Thermal Photonic Metamaterials Stable at 1873 K in Air 极端环境下的温度依赖红外工程:在1873 K空气中稳定的全介电热光子超材料。
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-21 DOI: 10.1007/s40820-025-02065-9
Yang Liu, He Lin, Yunxia Zhou, Liming Yuan, Yanqin Wang, Xiaoliang Ma, Cheng Huang, Xiangang Luo

Highlights

  • Temperature-dependent infrared engineering integrated with Pareto multi-objective optimization to simultaneously co-optimize spectral response, component, and structural efficiency.

  • All-dielectric thermal photonic metamaterials (TPMs, 5-layer & 2-μm) achieve 0.62/0.48 reflectivity (3–5/8–14 μm) for 82% radiative suppression (− 7.4 dB, 3–5 μm in atmosphere) and 0.87 emissivity (5–8 μm) for 10.1 kW m−2 radiative cooling.

  • The integrated all-dielectric TPM delivers 40%–50% radiative suppression and 40–60 K cooling at 1100 K, withstands > 20 thermal shocks (> 150 K s−1), and maintains 78% visible & 98% microwave transmittance.

由于热光子超材料(TPMs)固有的光学性能、热稳定性和机械完整性之间的权衡,极端环境红外工程技术的发展仍然是一个艰巨的挑战。这项工作介绍了一种新的多目标设计框架,并演示了在高达1873 K的极端温度下工作的TPM的设计,制造和验证。我们建立了一个集成温度相关神经网络和Pareto多目标优化的整体设计框架,以共同优化光谱响应、组件轻量化和结构效率。该框架的计算速度比遗传算法快100倍。在不同的大气模式和探测距离下,对所设计的TPM进行了性能评估。在1200-1500 K范围内,TPM实现了82%的峰值亮度抑制效率和- 7.4 dB的最大衰减。实验中,我们采用5层总厚度为2 μm的难熔TiO2/BeO多层堆叠制备了全介电TPM。优化后的结构具有较高的辐射抑制反射率(3-5 μm处为0.62,8-14 μm处为0.48)和辐射冷却发射率(5-8 μm处为0.87)。TPM在空气中承受1873 K 12小时,光谱漂移小于3%,保持优异的机械性能。在高温组件上,它在1100 K下实现40-50%的辐射抑制和40-60 K (~ 10.1 kW m-2)的辐射冷却,承受20次以上的热冲击循环(> 150 K s- 1,700 -1500 K),并在5个循环中保持稳定的性能,78%的可见光和98%的微波透过率。这项工作为极端环境下光子材料的设计和应用建立了一个新的范例。
{"title":"Temperature-Dependent Infrared Engineering for Extreme Environments: All-Dielectric Thermal Photonic Metamaterials Stable at 1873 K in Air","authors":"Yang Liu,&nbsp;He Lin,&nbsp;Yunxia Zhou,&nbsp;Liming Yuan,&nbsp;Yanqin Wang,&nbsp;Xiaoliang Ma,&nbsp;Cheng Huang,&nbsp;Xiangang Luo","doi":"10.1007/s40820-025-02065-9","DOIUrl":"10.1007/s40820-025-02065-9","url":null,"abstract":"<div><h2>Highlights</h2><div>\u0000 \u0000 <ul>\u0000 <li>\u0000 <p>Temperature-dependent infrared engineering integrated with Pareto multi-objective optimization to simultaneously co-optimize spectral response, component, and structural efficiency.</p>\u0000 </li>\u0000 <li>\u0000 <p>All-dielectric thermal photonic metamaterials (TPMs, 5-layer &amp; 2-μm) achieve 0.62/0.48 reflectivity (3–5/8–14 μm) for 82% radiative suppression (− 7.4 dB, 3–5 μm in atmosphere) and 0.87 emissivity (5–8 μm) for 10.1 kW m<sup>−2</sup> radiative cooling.</p>\u0000 </li>\u0000 <li>\u0000 <p>The integrated all-dielectric TPM delivers 40%–50% radiative suppression and 40–60 K cooling at 1100 K, withstands &gt; 20 thermal shocks (&gt; 150 K s<sup>−1</sup>), and maintains 78% visible &amp; 98% microwave transmittance.</p>\u0000 </li>\u0000 </ul>\u0000 </div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-025-02065-9.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146005492","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single-Atom Ru in CoFe-LDH Drives Efficient Charge Separation on BiVO4 for Solar Water Splitting 钴- ldh中单原子Ru驱动BiVO4高效电荷分离用于太阳能水分解
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-19 DOI: 10.1007/s40820-025-02062-y
Wenhui Deng, Gaoshuang He, Haozhi Zhou, Wenhao He, Lei Gan, Chenyu Zhang, Keke Wang, Xiaoqing Qiu, Yang Liu, Wenzhang Li

Highlights

  • The single Ru atoms trigger the electron rearrangement of Ru0.51-CoFe-LDH to engineer active sites and optimize interfacial energetics.

  • The negative shift of Ru0.51-CoFe-LDH band edge gives rise to more conspicuous band bending of the n-n junction formed with BiVO4.

  • The Ru0.51-CoFe-LDH/BiVO4 photoanode film displays a 3.1 times higher photocurrent density than bare BiVO4 and commendable charge collection efficiency (100%).

钒酸铋(BiVO4)被认为是一种很有前途的用于光电化学(PEC)水分解的光阳极。尽管在带隙和可见光响应方面具有优势,但由于严重的电荷重组,BiVO4表现出令人不满意的水分解效果。在此,我们阐明了一种创新的方法,涉及将单个Ru原子与CoFe-LDH助催化剂(Ru0.51-CoFe-LDH)结合并将其集成到BiVO4半导体衬底上。制备的ru0.51 - fe - ldh /BiVO4光阳极膜具有良好的电荷注入效率(76%)和电荷收集效率(100%)。有趣的是,氢和氧的产率以2:1的比例线性增加,照射140 min后分别达到158.6和67.4 μmol。根据实验表征和密度功能理论计算,这种显著的性能是由于单个Ru原子触发Ru0.51-CoFe-LDH的电子重排,从而设计活性位点并优化界面能量学。此外,ru0.51 - fe - ldh带边的负位移导致BiVO4形成的n-n结的带弯曲更加明显,加速了界面处光生电子-空穴对的分离和转移。本工作为在半导体衬底上构造单原子的PEC水分解体系提供了一个新的制备视角。
{"title":"Single-Atom Ru in CoFe-LDH Drives Efficient Charge Separation on BiVO4 for Solar Water Splitting","authors":"Wenhui Deng,&nbsp;Gaoshuang He,&nbsp;Haozhi Zhou,&nbsp;Wenhao He,&nbsp;Lei Gan,&nbsp;Chenyu Zhang,&nbsp;Keke Wang,&nbsp;Xiaoqing Qiu,&nbsp;Yang Liu,&nbsp;Wenzhang Li","doi":"10.1007/s40820-025-02062-y","DOIUrl":"10.1007/s40820-025-02062-y","url":null,"abstract":"<div><h2>Highlights</h2><div>\u0000 \u0000 <ul>\u0000 <li>\u0000 <p>The single Ru atoms trigger the electron rearrangement of Ru<sub>0.51</sub>-CoFe-LDH to engineer active sites and optimize interfacial energetics.</p>\u0000 </li>\u0000 <li>\u0000 <p>The negative shift of Ru<sub>0.51</sub>-CoFe-LDH band edge gives rise to more conspicuous band bending of the n-n junction formed with BiVO<sub>4</sub>.</p>\u0000 </li>\u0000 <li>\u0000 <p>The Ru<sub>0.51</sub>-CoFe-LDH/BiVO<sub>4</sub> photoanode film displays a 3.1 times higher photocurrent density than bare BiVO<sub>4</sub> and commendable charge collection efficiency (100%).</p>\u0000 </li>\u0000 </ul>\u0000 </div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-025-02062-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145994863","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Scalable Fabrication of Large-Scale Electrochromic Smart Windows for Superior Solar Radiation Regulation and Energy Savings 大规模电致变色智能窗户的可扩展制造,用于优越的太阳辐射调节和节能
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-16 DOI: 10.1007/s40820-025-02055-x
Yanbang Tang, Junyu Yuan, Rongzong Zheng, Chunyang Jia

Electrochromic smart windows (ESWs) can significantly reduce building energy consumption, but the high cost hinders large-scale production. The in situ growth of tungsten oxide (WO3) films is only by a simple immersion process, the silver nanowires (AgNWs) undergo oxidation to Ag+ ions through electron loss, and the liberated electrons provide driving force for the deposition of WO42−. Enabled the fabrication of large-area WO3 films and ESWs were fabricated under minimal laboratory conditions, demonstrating the economic feasibility, efficient and reliable nature of industrial production. Structural characterization and density functional theory calculations were combined to confirm that AgNWs effectively regulate oxygen vacancies of WO3 films and promote the in situ growth process. The optimized WO3 exhibits a maximum transmittance modulation of 90.8% and excellent cycling stability of 20,000 cycles. The large-scale WO3-based ESWs can save building energy up to 140.0 MJ m−2 compared to traditional windows in tropical regions, as verified by simulations more than 40 global cities. This research provides a new approach for improving the performance and industrial production of ESW, providing the full understanding and development direction to short the distance of the ESW commercial production.

电致变色智能窗(ESWs)可以显著降低建筑能耗,但其高成本阻碍了大规模生产。氧化钨(WO3)薄膜的原位生长仅通过简单的浸渍过程,银纳米线(AgNWs)通过电子损失被氧化为Ag+离子,释放的电子为WO42−的沉积提供动力。实现了大面积WO3薄膜的制备,并在最小的实验室条件下制备了ESWs,展示了工业生产的经济可行性、效率和可靠性。结合结构表征和密度泛函理论计算,证实AgNWs能有效调节WO3薄膜的氧空位,促进原位生长过程。优化后的WO3具有90.8%的最大透过率调制和20,000次的优良循环稳定性。通过对全球40多个城市的模拟验证,与热带地区的传统窗户相比,基于wo3的大规模ESWs可节省高达140.0 MJ m−2的建筑能源。本研究为提高ESW的性能和工业化生产提供了新的途径,为缩短ESW的商业化生产距离提供了充分的认识和发展方向。
{"title":"Scalable Fabrication of Large-Scale Electrochromic Smart Windows for Superior Solar Radiation Regulation and Energy Savings","authors":"Yanbang Tang,&nbsp;Junyu Yuan,&nbsp;Rongzong Zheng,&nbsp;Chunyang Jia","doi":"10.1007/s40820-025-02055-x","DOIUrl":"10.1007/s40820-025-02055-x","url":null,"abstract":"<div><p>Electrochromic smart windows (ESWs) can significantly reduce building energy consumption, but the high cost hinders large-scale production. The in <i>situ</i> growth of tungsten oxide (WO<sub>3</sub>) films is only by a simple immersion process, the silver nanowires (AgNWs) undergo oxidation to Ag<sup>+</sup> ions through electron loss, and the liberated electrons provide driving force for the deposition of WO<sub>4</sub><sup>2−</sup>. Enabled the fabrication of large-area WO<sub>3</sub> films and ESWs were fabricated under minimal laboratory conditions, demonstrating the economic feasibility, efficient and reliable nature of industrial production. Structural characterization and density functional theory calculations were combined to confirm that AgNWs effectively regulate oxygen vacancies of WO<sub>3</sub> films and promote the in situ growth process. The optimized WO<sub>3</sub> exhibits a maximum transmittance modulation of 90.8% and excellent cycling stability of 20,000 cycles. The large-scale WO<sub>3</sub>-based ESWs can save building energy up to 140.0 MJ m<sup>−2</sup> compared to traditional windows in tropical regions, as verified by simulations more than 40 global cities. This research provides a new approach for improving the performance and industrial production of ESW, providing the full understanding and development direction to short the distance of the ESW commercial production.</p>\u0000<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-025-02055-x.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145972335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dual Chloride Confinement in Noble Metal‐Doped NiV LDH Catalysts Enables Stable Industrial-Level Seawater Electrolysis 双氯化物约束在贵金属掺杂的NiV LDH催化剂中实现稳定的工业级海水电解
IF 36.3 1区 材料科学 Q1 Engineering Pub Date : 2026-01-16 DOI: 10.1007/s40820-026-02067-1
Kai Liu, Yaohai Cai, Xiaotian Wei, Lihang Qu, Jianxi Lu, Yingwei Qi, Zhenbo Wang, Dong Liu

Highlights

  • Noble metal doping into NiV-layered double hydroxides optimizes the electronic structure of active sites, significantly enhancing its catalytic performance for the hydrogen evolution reaction and oxygen evolution reaction.

  • A “dual chloride confinement” strategy is proposed to overcome chloride corrosion in seawater electrolysis by synergizing strong adsorption (Ir-Cl) with electrostatic repulsion (VO43−).

  • Offers a practical route toward economically viable and sustainable hydrogen production from seawater.

在niv层状双氧水化物中掺杂贵金属,优化了活性位点的电子结构,显著提高了其析氢反应和析氧反应的催化性能。提出了一种“双氯化物约束”策略,通过强吸附(Ir-Cl)和静电排斥(VO43−)协同作用来克服海水电解中的氯化物腐蚀。为经济上可行和可持续的海水制氢提供了一条实用的途径。
{"title":"Dual Chloride Confinement in Noble Metal‐Doped NiV LDH Catalysts Enables Stable Industrial-Level Seawater Electrolysis","authors":"Kai Liu,&nbsp;Yaohai Cai,&nbsp;Xiaotian Wei,&nbsp;Lihang Qu,&nbsp;Jianxi Lu,&nbsp;Yingwei Qi,&nbsp;Zhenbo Wang,&nbsp;Dong Liu","doi":"10.1007/s40820-026-02067-1","DOIUrl":"10.1007/s40820-026-02067-1","url":null,"abstract":"<div><h2>Highlights</h2><div>\u0000 \u0000 <ul>\u0000 <li>\u0000 <p>Noble metal doping into NiV-layered double hydroxides optimizes the electronic structure of active sites, significantly enhancing its catalytic performance for the hydrogen evolution reaction and oxygen evolution reaction.\u0000</p>\u0000 </li>\u0000 <li>\u0000 <p>A “dual chloride confinement” strategy is proposed to overcome chloride corrosion in seawater electrolysis by synergizing strong adsorption (Ir-Cl) with electrostatic repulsion (VO<sub>4</sub><sup>3−</sup>).</p>\u0000 </li>\u0000 <li>\u0000 <p>Offers a practical route toward economically viable and sustainable hydrogen production from seawater.</p>\u0000 </li>\u0000 </ul>\u0000 </div></div>","PeriodicalId":714,"journal":{"name":"Nano-Micro Letters","volume":"18 1","pages":""},"PeriodicalIF":36.3,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s40820-026-02067-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145972337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Nano-Micro Letters
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.
×
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