Science China Materials最新文献

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Stress-induced anisotropy for MHz-stable permeability in Fe-based nanocrystalline alloys 应力诱导的铁基纳米晶合金mhz稳定磁导率的各向异性
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-02-06 DOI: 10.1007/s40843-025-3883-2
Zhijun Guo  (, ), Jifeng Zhou  (, ), Qianqian Liu  (, ), Mingjuan Cai  (, ), Yanzhou Fan  (, ), Qiang Luo  (, ), Baolong Shen  (, )
{"title":"Stress-induced anisotropy for MHz-stable permeability in Fe-based nanocrystalline alloys","authors":"Zhijun Guo \u0000 (,&nbsp;),&nbsp;Jifeng Zhou \u0000 (,&nbsp;),&nbsp;Qianqian Liu \u0000 (,&nbsp;),&nbsp;Mingjuan Cai \u0000 (,&nbsp;),&nbsp;Yanzhou Fan \u0000 (,&nbsp;),&nbsp;Qiang Luo \u0000 (,&nbsp;),&nbsp;Baolong Shen \u0000 (,&nbsp;)","doi":"10.1007/s40843-025-3883-2","DOIUrl":"10.1007/s40843-025-3883-2","url":null,"abstract":"<div><p>Tensile stress annealing (TSA) is an effective strategy for tailoring magnetic anisotropy and high-frequency performance in nanocrystalline soft magnetic alloys. Here, we systematically investigate the influence of TSA on the microstructure, magnetic domain evolution, and permeability stability of Fe<sub>69.5</sub>Co<sub>3</sub>Nb<sub>2</sub>Mo<sub>1.5</sub>Si<sub>14</sub>B<sub>9</sub>Cu<sub>1</sub> nanocrystalline alloys. Across all applied stresses (0–300 MPa), the alloys retain an ultrafine grain size (⩽11 nm), yet the induced uniaxial anisotropy constant (<i>K</i><sub>u</sub>) rises sharply from 22.5 to 665 J/m<sup>3</sup>. This increase in <i>K</i><sub>u</sub> refines the magnetic domain structure, reducing average domain width from 110 to 36 µm, and shifts the magnetization mechanism from domain-wall displacement to rotation-dominated reversal. Quantitative correlation between <i>K</i><sub>u</sub>, domain structure, and effective permeability (<i>μ</i><sub>e</sub>) reveals that higher stress suppresses <i>μ</i><sub>e</sub> at low frequencies but yields exceptional frequency stability: <i>μ</i><sub>e</sub> ≈ 2330 is maintained up to 1 MHz at 50 MPa, and <i>μ</i><sub>e</sub> ≈ 585 remains constant from 1 kHz to 10 MHz at 300 MPa. These findings demonstrate that stress-induced anisotropy is a decisive factor in governing high-frequency magnetic response, offering both mechanistic insight and a practical framework for designing next-generation soft magnetic materials for precision current transformers, EMC filters, and MHz-class power electronics.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1518 - 1528"},"PeriodicalIF":7.4,"publicationDate":"2026-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352837","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
Synthesis of transition metal nitride nanomaterials for electrocatalytic applications 电催化用过渡金属氮化纳米材料的合成
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-02-03 DOI: 10.1007/s40843-026-4022-7
Shuai Zhang  (, ), Yiming Wang  (, ), Jiezhou Wang  (, ), Xixi Wang  (, ), Yiyao Ge  (, )
{"title":"Synthesis of transition metal nitride nanomaterials for electrocatalytic applications","authors":"Shuai Zhang \u0000 (,&nbsp;),&nbsp;Yiming Wang \u0000 (,&nbsp;),&nbsp;Jiezhou Wang \u0000 (,&nbsp;),&nbsp;Xixi Wang \u0000 (,&nbsp;),&nbsp;Yiyao Ge \u0000 (,&nbsp;)","doi":"10.1007/s40843-026-4022-7","DOIUrl":"10.1007/s40843-026-4022-7","url":null,"abstract":"<div><p>Transition metal nitrides (TMNs) have been considered as promising alternative catalysts to noble metals in various electrocatalytic applications due to their noble metal-like electronic structures, high conductivity, low cost, as well as strong chemical stability, which could resist corrosion and oxidation in harsh operation conditions. Therefore, the rational design and controlled synthesis of TMNs with distinct structures play a vital role in developing highly efficient electrocatalysts toward electrochemical applications. This review provides a comprehensive summary of representative synthetic strategies for TMNs, such as direct nitridation, solid-state reaction, sol-gel assisted reaction, and wet-chemical reaction, presents the distinct structural characterizations, and demonstrates their advances in the electrochemical applications. Finally, we propose the remaining challenges and the future research directions on the exploration of TMNs with well-defined structures for electrocatalytic applications, which could shed light on the future development of high-performance electrocatalysts.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1291 - 1316"},"PeriodicalIF":7.4,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352705","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
Interface engineering of MXenes for flexible energy storage and harvesting 基于MXenes的柔性能量存储与收集接口工程
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-01-28 DOI: 10.1007/s40843-025-3836-8
Si Chen  (, ), Libo Chang  (, ), Guozheng Zhang  (, ), Wenke Xie  (, ), Xu Xiao  (, )
{"title":"Interface engineering of MXenes for flexible energy storage and harvesting","authors":"Si Chen \u0000 (,&nbsp;),&nbsp;Libo Chang \u0000 (,&nbsp;),&nbsp;Guozheng Zhang \u0000 (,&nbsp;),&nbsp;Wenke Xie \u0000 (,&nbsp;),&nbsp;Xu Xiao \u0000 (,&nbsp;)","doi":"10.1007/s40843-025-3836-8","DOIUrl":"10.1007/s40843-025-3836-8","url":null,"abstract":"<div><p>Flexible energy storage and harvesting devices, as core components of the flexible electronic system, have driven the transformation of electronic system from “external power supply” to “self-powering” and from “fixed forms” to “adaptive configurations”, thus playing an important role in the advancement of wearable technology, the internet of things, and other related fields. MXenes, a class of two-dimensional transition metal carbides, nitrides, and carbonitrides, emerge as promising candidates for flexible energy storage and harvesting devices, attributed to their excellent conductivity, mechanical flexibility, and tunable interfacial characteristics. Specifically, the interfacial characteristics of MXenes, including surface energy, surface terminations, and interlayer spacing, have a decisive influence on the performance of MXene-based energy devices. This review summarizes the influence of microcosmic interfacial characteristics on macroscopic properties, the interfacial regulation strategies, and applications in flexible energy storage and harvesting of MXenes, concluding with current challenges and perspectives to guide the design of high-performance MXene-based energy devices.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1265 - 1290"},"PeriodicalIF":7.4,"publicationDate":"2026-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352769","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
Surface-confined metallization of nanofibrous networks via selective dissolution-assisted transfer printing for lightweight and air-permeable soft electronics 轻量化和透气性软电子产品用选择性溶解辅助转移印刷纳米纤维网络的表面限制金属化
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-01-23 DOI: 10.1007/s40843-025-3838-5
Weiyan Li  (, ), Zhongqian Song  (, ), Xiyue Zhang  (, ), Huijun Kong  (, ), Cuiyu Liu  (, ), Xue Li  (, ), Xiaotong Sun  (, ), Zhaofu Zhang  (, ), Li Niu  (, )
{"title":"Surface-confined metallization of nanofibrous networks via selective dissolution-assisted transfer printing for lightweight and air-permeable soft electronics","authors":"Weiyan Li \u0000 (,&nbsp;),&nbsp;Zhongqian Song \u0000 (,&nbsp;),&nbsp;Xiyue Zhang \u0000 (,&nbsp;),&nbsp;Huijun Kong \u0000 (,&nbsp;),&nbsp;Cuiyu Liu \u0000 (,&nbsp;),&nbsp;Xue Li \u0000 (,&nbsp;),&nbsp;Xiaotong Sun \u0000 (,&nbsp;),&nbsp;Zhaofu Zhang \u0000 (,&nbsp;),&nbsp;Li Niu \u0000 (,&nbsp;)","doi":"10.1007/s40843-025-3838-5","DOIUrl":"10.1007/s40843-025-3838-5","url":null,"abstract":"<div><p>Air-permeable and ultrathin conductive electrodes are essential for next-generation soft electronics, including breathable wearables, on-skin devices and bio-integrated electronics. However, conventional metallization strategies, such as sputtering and ink-printing, often suffer from severe vertical charge leakage due to the porous and ultrathin characteristics of nanofibrous networks, leading to device short-circuiting, operational failure and limited vertical integration. Here, we present a solvent-selective dissolution-assisted transfer printing strategy to achieve surface-confined metallization of ultrathin, lightweight, and gas-permeable nanofibrous networks, enabling lateral conductivity while maintaining vertical insulation. This transfer printing process facilitates not only the rapid formation of conductive patterns on the surface of nanofibrous networks but also mechanical reinforcement through solvent evaporation-induced interlocked fiber-fiber welding. Meanwhile, the strategy preserves the high permeability of the nanofibrous networks and imparts a unique combination of surface conductivity (2 Ω cm) and vertical insulativity (10<sup>11</sup> Ω cm). The resulting anisotropic conductive networks enable low-voltage wearable heaters, high-sensitive pressure sensors, and ultralight temperature sensors. A pressure-temperature dual-modal sensing patch is further fabricated for intelligent grasping classification. The proposed surface-confined metallization strategy enables rapid fabrication of an anisotropic conductive network as a building block to construct air-permeable, ultrathin and lightweight wearable electronics.\u0000</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1600 - 1612"},"PeriodicalIF":7.4,"publicationDate":"2026-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352675","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
Spatially decoupled single/dual-atomic sites with independent bifunctional activity for high-performance fiber zinc-air batteries 具有独立双功能活性的空间解耦单/双原子位置用于高性能纤维锌空气电池
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-01-23 DOI: 10.1007/s40843-025-3805-1
Jing Zhou  (, ), Yumin Chen  (, ), Wei Mao  (, ), Long Jiang  (, ), Huangjian Chen  (, ), Yunzhan Ying  (, ), Yulong Wan  (, ), Shifan Zheng  (, ), Ju Lin  (, ), Shikun Liang  (, ), Yuyuan Yao  (, ), Bingjie Wang  (, ), Ye Zhang  (, ), Lihua Gan  (, ), Huisheng Peng  (, ), Lie Wang  (, )
{"title":"Spatially decoupled single/dual-atomic sites with independent bifunctional activity for high-performance fiber zinc-air batteries","authors":"Jing Zhou \u0000 (,&nbsp;),&nbsp;Yumin Chen \u0000 (,&nbsp;),&nbsp;Wei Mao \u0000 (,&nbsp;),&nbsp;Long Jiang \u0000 (,&nbsp;),&nbsp;Huangjian Chen \u0000 (,&nbsp;),&nbsp;Yunzhan Ying \u0000 (,&nbsp;),&nbsp;Yulong Wan \u0000 (,&nbsp;),&nbsp;Shifan Zheng \u0000 (,&nbsp;),&nbsp;Ju Lin \u0000 (,&nbsp;),&nbsp;Shikun Liang \u0000 (,&nbsp;),&nbsp;Yuyuan Yao \u0000 (,&nbsp;),&nbsp;Bingjie Wang \u0000 (,&nbsp;),&nbsp;Ye Zhang \u0000 (,&nbsp;),&nbsp;Lihua Gan \u0000 (,&nbsp;),&nbsp;Huisheng Peng \u0000 (,&nbsp;),&nbsp;Lie Wang \u0000 (,&nbsp;)","doi":"10.1007/s40843-025-3805-1","DOIUrl":"10.1007/s40843-025-3805-1","url":null,"abstract":"<div><p>The development of high-performance bifunctional electrocatalysts is crucial for advancing zinc-air batteries. However, the fundamentally distinct mechanisms of the oxygen reduction and evolution reactions (ORR/OER) hinder the simultaneous realization of high activity within a single catalyst. Herein, we propose a spatial decoupling strategy to overcome this limitation by engineering isolated Fe single-atoms and Fe–Ir dual-atom pairs on a nitrogen-doped carbon matrix (Fe/FeIr-NC). In this architecture, Fe single atoms serve as ORR centers, while Fe–Ir pairs with tunable spacing are tailored for OER, enabling complete functional separation and independent optimization of the reactions. As a result, the catalyst delivers an ORR half-wave potential of 0.91 V and an OER overpotential of 250 mV at 10 mA cm<sup>−2</sup>, yielding a record-low bifunctional gap (Δ<i>E</i> = 0.57 V) that outperforms all reported single- and dual-atom catalysts. A flexible fiber zinc-air battery was developed based on this catalyst, delivering a peak power density of 3920 W kg<sup>−1</sup>, along with a 1.4-fold increase in energy efficiency and a 2.6-fold extension in cycle life compared to the commercial Pt/C + IrO<sub>2</sub> benchmark. This work not only breaks the traditional activity trade-off in bi-functional catalysis but also offers a promising route toward high-performance power sources for wearable electronics.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1581 - 1589"},"PeriodicalIF":7.4,"publicationDate":"2026-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352674","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
Smart fiber photodetectors based on inorganic semiconductors 基于无机半导体的智能光纤光电探测器
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-01-22 DOI: 10.1007/s40843-025-3947-3
Hongyun Peng  (, ), Fangfang Xia  (, ), Zhigang Xia  (, ), Huiqiao Li  (, ), Tianyou Zhai  (, )
{"title":"Smart fiber photodetectors based on inorganic semiconductors","authors":"Hongyun Peng \u0000 (,&nbsp;),&nbsp;Fangfang Xia \u0000 (,&nbsp;),&nbsp;Zhigang Xia \u0000 (,&nbsp;),&nbsp;Huiqiao Li \u0000 (,&nbsp;),&nbsp;Tianyou Zhai \u0000 (,&nbsp;)","doi":"10.1007/s40843-025-3947-3","DOIUrl":"10.1007/s40843-025-3947-3","url":null,"abstract":"<div><p>Fiber photodetectors (FPDs) with high deformability, flexible designability, and seamless integrability with everyday textiles hold tremendous potential for the next-generation wearable optoelectronics. Inorganic semiconductors (ISCs) are considered the ideal building block to design and govern the functions of FPDs owing to their superior electrical and optical properties. Recent developments in wearable technology of ISCs, especially in fiber form factor, have driven the creation of various FPDs with smart capabilities, from light sensing, information interfacing, to sophisticated logic operating, revolutionizing human-machine interaction paradigms in many emerging fields. Herein, we present a comprehensive review of the recent progress of ISC-based FPDs. Firstly, key design principles for ISC-based FPDs are explored, encompassing material selection, fabrication technologies, device architectures, and textile integration strategies. Then, how defect engineering, alignment engineering, and heterojunction engineering of ISCs can control the optoelectronic performance of FPDs is examined. Following this, potential wearable applications of ISC-based FPDs in optical communication, image sensing, and health monitoring are analyzed. Finally, the challenges and perspectives for the design of high-performance ISC-based FPDs are outlined.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1249 - 1264"},"PeriodicalIF":7.4,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352704","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
Interface-engineered NiCo sites on natural wood-derived porous carbon substrate for efficient paired electrocatalysis 界面工程NiCo位点在天然木材衍生的多孔碳基材上用于高效成对电催化
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-01-22 DOI: 10.1007/s40843-025-3815-0
Junhua Kuang  (, ), Siwang Zhang  (, ), Shuliang Yang  (, ), Jinlong Wan  (, ), Junchi Ma  (, ), Shihang Zhu  (, ), Hangyong Ye  (, ), Zifan Li  (, ), Ziyan Wang  (, ), Yuting Zhang  (, ), Guangkuo Xu  (, ), Jiaran Li  (, ), Li Peng  (, ), Shisheng Zheng  (, ), Jia Yu  (, ), Jian-Feng Li  (, )
{"title":"Interface-engineered NiCo sites on natural wood-derived porous carbon substrate for efficient paired electrocatalysis","authors":"Junhua Kuang \u0000 (,&nbsp;),&nbsp;Siwang Zhang \u0000 (,&nbsp;),&nbsp;Shuliang Yang \u0000 (,&nbsp;),&nbsp;Jinlong Wan \u0000 (,&nbsp;),&nbsp;Junchi Ma \u0000 (,&nbsp;),&nbsp;Shihang Zhu \u0000 (,&nbsp;),&nbsp;Hangyong Ye \u0000 (,&nbsp;),&nbsp;Zifan Li \u0000 (,&nbsp;),&nbsp;Ziyan Wang \u0000 (,&nbsp;),&nbsp;Yuting Zhang \u0000 (,&nbsp;),&nbsp;Guangkuo Xu \u0000 (,&nbsp;),&nbsp;Jiaran Li \u0000 (,&nbsp;),&nbsp;Li Peng \u0000 (,&nbsp;),&nbsp;Shisheng Zheng \u0000 (,&nbsp;),&nbsp;Jia Yu \u0000 (,&nbsp;),&nbsp;Jian-Feng Li \u0000 (,&nbsp;)","doi":"10.1007/s40843-025-3815-0","DOIUrl":"10.1007/s40843-025-3815-0","url":null,"abstract":"<div><p>The development of bifunctional electrocatalysts capable of integrating biomass-derived platform molecule oxidation with organic reduction offers a promising strategy for simultaneously enhancing energy efficiency and generating high-value chemicals. However, designing catalysts that exhibit both high activity and stability in integrated systems remains a significant challenge. Herein, we report a self-supported electrode composed of nitrogen-doped carbonized wood (NCW) supported NiCo nanosheets (NiCo<sub>0.3</sub>/NCW) that enables the electrocatalytic 5-hydroxymethylfurfural oxidation to produce 2,5-furandicarboxylic acid (FDCA) and the nitrobenzene reduction to yield aniline in an integrated electrochemical cell. The NiCo<sub>0.3</sub>/NCW electrode achieves the production of FDCA and aniline at a low cell voltage of 1.7 V, with ∼99% anodic and ∼92% cathodic Faradaic efficiencies, respectively. Experimental characterizations disclose that the hierarchical porous NCW architecture promotes the dispersion of active sites, while nitrogen doping strengthens metal-support interactions. <i>In-situ</i> spectroscopic experiments combined with density functional theory (DFT) calculations reveal that cobalt incorporation tunes the electronic structure of nickel, thus optimizing substrate and intermediate adsorption, and lowering energy barriers. These effects ultimately enhance the performance of the natural wood-derived catalyst in integrated biomass valorization and selective organic electrosynthesis.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1562 - 1572"},"PeriodicalIF":7.4,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352673","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
Revolutionizing healthcare: the next generation of wearable chemical sensors for personal health monitoring 革命性的医疗保健:用于个人健康监测的下一代可穿戴化学传感器
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-01-15 DOI: 10.1007/s40843-025-3780-3
Lei Tang  (, ), Jianshu Zheng  (, ), Zhaolei Li  (, ), Feiyang Liu  (, ), Lingyun Wang  (, ), William W. Yu  (, )
{"title":"Revolutionizing healthcare: the next generation of wearable chemical sensors for personal health monitoring","authors":"Lei Tang \u0000 (,&nbsp;),&nbsp;Jianshu Zheng \u0000 (,&nbsp;),&nbsp;Zhaolei Li \u0000 (,&nbsp;),&nbsp;Feiyang Liu \u0000 (,&nbsp;),&nbsp;Lingyun Wang \u0000 (,&nbsp;),&nbsp;William W. Yu \u0000 (,&nbsp;)","doi":"10.1007/s40843-025-3780-3","DOIUrl":"10.1007/s40843-025-3780-3","url":null,"abstract":"<div><p>Real-time health monitoring and ongoing evaluation of physiological conditions are becoming increasingly vital for the advancement of future medical diagnostics and personalized healthcare solutions. Given that certain illnesses necessitate prompt and accessible detection methods, wearable chemical sensors have garnered considerable interest for their capability to monitor health through physiological signals and chemical indicators. This review delivers a thorough examination of recent developments in four primary categories of wearable chemical sensors: biosensors, humidity sensors, gas sensors, and ion sensors. We explore the representative materials, device structures, operating mechanisms, and various application scenarios for each type of sensor. By investigating the latest innovations in these technologies, we aim to provide a detailed overview of the current research landscape, highlight existing challenges, and present potential future directions of wearable chemical sensors in healthcare monitoring.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1394 - 1415"},"PeriodicalIF":7.4,"publicationDate":"2026-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352874","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
Synergistic dual supramolecular interactions enhance ionic thermoelectric performance in dilute-electrolyte hydrogels 协同双超分子相互作用增强了稀电解质水凝胶中的离子热电性能
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-01-14 DOI: 10.1007/s40843-025-3689-9
Hongbing Li  (, ), Zhangjie Gu  (, ), Shuyang Sheng  (, ), Yongping Chai  (, ), Zhaoyang Jiao  (, ), Fang Zheng  (, ), Xiaodong Chi  (, )
{"title":"Synergistic dual supramolecular interactions enhance ionic thermoelectric performance in dilute-electrolyte hydrogels","authors":"Hongbing Li \u0000 (,&nbsp;),&nbsp;Zhangjie Gu \u0000 (,&nbsp;),&nbsp;Shuyang Sheng \u0000 (,&nbsp;),&nbsp;Yongping Chai \u0000 (,&nbsp;),&nbsp;Zhaoyang Jiao \u0000 (,&nbsp;),&nbsp;Fang Zheng \u0000 (,&nbsp;),&nbsp;Xiaodong Chi \u0000 (,&nbsp;)","doi":"10.1007/s40843-025-3689-9","DOIUrl":"10.1007/s40843-025-3689-9","url":null,"abstract":"<div><p>Converting body heat into electricity presents an appealing route for sustainably powering wearable electronics; however, conventional thermoelectric materials face significant drawbacks, including high ionic concentrations, toxicity, and limited thermoelectric efficiency. Here, we report an ionic thermoelectric hydrogel designed through precise supramolecular chemistry, utilizing dual molecular interactions, host-guest complexation of α-cyclodextrin (α-CD) with I<sub>3</sub><sup>−</sup> ions and hydrogen bonding between polyvinyl alcohol (PVA) polymer chains and I<sub>3</sub><sup>−</sup>. This molecularly tailored approach markedly amplifies thermoelectric performance, achieving a high thermopower of 2.21 mV/K and a tenfold enhancement in peak power output at an exceptionally low iodine concentration (10 mmol/L I<sup>−</sup> + 2.5 mmol/L I<sub>3</sub><sup>−</sup>). The hydrogel maintains excellent biocompatibility and mechanical robustness, suitable for direct skin contact. Demonstrated applications include flexible thermoelectric devices generating nearly 100 mV from body heat and sensor arrays capable of motion and spatial temperature sensing. These results underscore the substantial potential of supramolecularly designed ionic thermoelectric hydrogels for wearable energy harvesting, personalized healthcare monitoring, and advanced human-computer interfaces.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"69 3","pages":"1647 - 1653"},"PeriodicalIF":7.4,"publicationDate":"2026-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352871","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
Recyclable, reprocessable, and biodegradable cellulosic bioplastics enabled by a reactive eutectic network 可回收,可再加工,可生物降解的纤维素生物塑料,通过反应共晶网络实现
IF 7.4 2区 材料科学
Science China Materials Pub Date : 2026-01-14 DOI: 10.1007/s40843-025-3871-9
Huanhuan Wu  (, ), Ren’ai Li  (, )
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