{"title":"Enzyme‐Based Electrochemical Sensing Systems for On‐Site Detection: Recent Progress and Prospects","authors":"Huiwen Wang, Cong Liu, Tingting Feng, Yanfei Zhang, Yanfang Wu, Zong Dai, Changqing Yi","doi":"10.1002/smll.202507926","DOIUrl":"https://doi.org/10.1002/smll.202507926","url":null,"abstract":"The growing demand for rapid and reliable health monitoring drives significant advancements in enzyme‐based electrochemical sensors for point‐of‐care testing (POCT) applications. This review highlights recent developments in enzyme electrode technology, with a focus on surface modifications, immobilization techniques, and electrode materials that significantly enhance sensor stability, sensitivity, and accuracy in detecting critical health biomarkers. The integration of these electrochemical sensors with portable devices and smart technologies, enabled by innovative hardware and software designs, positions them as highly practical tools for clinical diagnostics and health monitoring. Despite these advances, several challenges persist in ensuring their broad applicability in diverse environments. This review explores these challenges and discusses future research directions. By providing these insights into current innovations and future possibilities, this review aims to serve as a valuable resource for researchers and foster the continued development of enzyme‐based electrochemical sensors in healthcare applications.","PeriodicalId":228,"journal":{"name":"Small","volume":"108 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145235440","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}
SmallPub Date : 2025-10-06DOI: 10.1002/smll.202507522
Ali Mohammadi,Hanseung Kim,Mohammad Javad Arshia,Soobin Han,Abilash Sedhumadhavan,Reza Maleki,A T Ezhil Vilian,Arun Prakash Periasamy,Yun Suk Huh,Young-Kyu Han
{"title":"Bifunctional Fe─Ru─VC Catalyst for Energy Efficient Tandem Alkaline Electrolysis of Hydrazine and 4-nitrophenol.","authors":"Ali Mohammadi,Hanseung Kim,Mohammad Javad Arshia,Soobin Han,Abilash Sedhumadhavan,Reza Maleki,A T Ezhil Vilian,Arun Prakash Periasamy,Yun Suk Huh,Young-Kyu Han","doi":"10.1002/smll.202507522","DOIUrl":"https://doi.org/10.1002/smll.202507522","url":null,"abstract":"Alternate electrocatalytic reactions can turn pollutants into green fuels, offering an energy-efficient approach. Coupling hydrazine oxidation reaction (HzOR), with 4-nitrophenol hydrogenation (4-NPHR) is especially promising. Here, we report a bifunctional electrocatalyst composed of defect-rich Fe-Ru alloy clusters uniformly anchored on vanadium carbide (Fe─Ru─VC), synthesized via scalable ball milling and thermal annealing. Fe─Ru─VC exhibits excellent electrocatalytic activity toward both HzOR and 4-NPHR, requiring a low overpotential of 145 mV at 10 mA cm-2 and a favorable Tafel slope of 68.9 mV dec-1 for HzOR, with stability exceeding 90 h in 1M KOH. For 1 mM 4-NPHR, superior Fe-Ru-VC performance is achieved -7.2 mA cm-2 at 100 mV, highlighting its high efficiency. Furthermore, a paired H-cell electrolyzer (HzOR||4-NPHR) operates at only 200 mV to deliver 40 mA cm-2, underscoring its low energy demand. In situ Raman spectroscopy confirms the formation of Fe─Ru(OOH) as active sites, UV-Vis analysis confirms rapid 4-NP degradation, and DFT calculations demonstrate enhanced electronic interactions at the Ru─Fe junction, consistent with experimental observations. The outstanding activity is attributed to synergistic Fe-Ru interactions, the presence of zigzag edge defects, and the excellent conductivity of the VC support.","PeriodicalId":228,"journal":{"name":"Small","volume":"86 1","pages":"e07522"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229125","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}
{"title":"Milliwatt-Scale Moisture-Induced Power Generation via Cation Intercalation in Sodium Vanadium Oxide Nanobelts.","authors":"Hyerim Baek,Minjae Song,Daewoong Kim,Dong Hyun Yoon,Kyung-Il Lee,Sangmin Jeon","doi":"10.1002/smll.202505223","DOIUrl":"https://doi.org/10.1002/smll.202505223","url":null,"abstract":"A moisture-induced power generator (MPG) with exceptionally high-power output and extended operational stability is developed by systematically integrating three active materials: A LiCl -containing hydrogel, a perforated aluminum sheet, and NaV3O8 (NVO) nanobelts. The LiCl-containing hydrogel, due to its hygroscopic nature, maintains a stable moisture gradient and supplies charge carriers (Li+ ions). Simultaneously, the perforated aluminum sheet acts as the primary source of charge carriers (Al3+ ions) without generating oppositely charged ions, thereby preventing the degradation of the potential difference caused by ion migration. The NVO nanobelts undergo a reduction reaction through the intercalation of Li+ and Al3+ ions into their layered structure, effectively preventing reverse migration by resolving charge accumulation and generating Faradaic currents. Furthermore, their elongated structure enables the formation of a high-surface, conductive active layer through entanglement with carbon black nanoparticles, eliminating the need for binder materials. This systematic design achieves a maximum open-circuit voltage of 1.64 V, a short-circuit current of 10.44 mA cm-2, and a power density of 2.13 mW cm-2 at a load resistance of 200 Ω under 90% relative humidity. These results represent a record-high performance among reported MPGs, highlighting significant advancements in efficiency and durability, thereby enhancing the feasibility of MPGs for practical applications.","PeriodicalId":228,"journal":{"name":"Small","volume":"1 1","pages":"e05223"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229189","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}
{"title":"Controlling the Oxidation State of Copper in Metal-Organic Frameworks for CO Electroreduction to Acetate.","authors":"Ying Jiao,Senlin Chu,Nengji Liu,Bo-Xin Zhang,Yang Hou,Xiang Zhao","doi":"10.1002/smll.202509324","DOIUrl":"https://doi.org/10.1002/smll.202509324","url":null,"abstract":"The electrochemical carbon monoxide reduction reaction (CORR) represents a promising approach for the conversion of CO into acetate. However, the efficiency and selectivity of CO-to-acetate conversion are hindered by the competing formation of other products. Here, a Cu-MFU-4l-F catalyst is reported that preserves mixed-valence Cu species through the introduction of halogens and a precise Cu─N3 coordination structure, facilitating efficient CORR with a Faradaic efficiency (FE) of 73.2% for acetate in a flow cell. Furthermore, the selectivity for acetate remained stable over 140 h in a membrane electrode assembly (MEA) electrolyzer. The X-ray absorption spectroscopy reveals that the coordination environment around Cu is retained during the catalysis. In situ ATR-FTIRS indicates that the introduction of fluorine enhanced surface *CO adsorption and key intermediate *OCCOH formation, facilitates asymmetric C─C coupling, and improves the selectivity for acetate.","PeriodicalId":228,"journal":{"name":"Small","volume":"37 1","pages":"e09324"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229121","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}
{"title":"Direct Observation of Spherulitic Covalent Triazine Frameworks Grown in Hot Superacid Matrices.","authors":"Tianhao Fang,Yifeng Xing,Huimin Wu,Duan Gao,Xiaomin Xu,Zhenghua Zhang,Huai-Zhen Wang,Zhen Chen","doi":"10.1002/smll.202509494","DOIUrl":"https://doi.org/10.1002/smll.202509494","url":null,"abstract":"As emerging porous crystalline polymers, 2D covalent organic frameworks present exclusively in macroscopic forms of polycrystalline powders, single crystals, or thin films. Here, spherulitic 2D covalent triazine frameworks (CTFs) grown in hot superacid matrices are grown, which exhibit a typical Maltese cross pattern of light extinction. A structural evolution from small-angle branched nanofibrils to a core-shell hemispherical geometry is real-time recorded by in situ microscopies and spectroscopies. Time-resolved imaging analysis on spherulitic growth unveils a nonclassical crystallization process, which involves a secondary nucleation-elongation mechanism coupled with amorphous-to-crystalline transition. Furthermore, fluorine doping into CTF enables acceleration of 2D template polymerization and shell formation to develop size-tunable spherulites, with the optimal size up to ≈48 µm in diameter. This work provides unique insights into 2D polymerization and crystallization processes via in situ characterization and demonstrates an unprecedented form of CTF crystallites, which are potentially used as ion sensors and storage.","PeriodicalId":228,"journal":{"name":"Small","volume":"8 1","pages":"e09494"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229144","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}
{"title":"Fluorine-Mediated Carbon Doping in Boron Nitride: Atomic-Level Interface Engineering for Balancing Microwave Absorption and Thermal Management.","authors":"Zhangwen Xie,Yufei Tang,Yagang Zhang,Wanxing Zheng,Yani Sun,Huan Zhong,Shiyu Zhang,Qingnan Meng,Kang Zhao","doi":"10.1002/smll.202506851","DOIUrl":"https://doi.org/10.1002/smll.202506851","url":null,"abstract":"The advancement of high-density integrated electronics urgently demands materials that integrate efficient thermal management and microwave absorption. However, conventional design strategies that often rely on materials with multi-component composites face a trade-off between these properties, and a lack of microwave absorption effectiveness study in the polymer matrix. Herein, a fluorine-mediated carbon doping in boron nitride (C-F-BN) is designed to achieve atomic-level interface engineering. Fluoride induces the formation of polarized C─F bonds and promotes ordered sp2-carbon incorporation, which well preserves the BN lattice integrity while establishing strong polarization sites. The resulting C-F-BN shows exceptional microwave absorption with a reflection loss of -43 dB at 2 mm thickness, compared to that of only carbon doping in BN, achieving an effective absorption bandwidth of 3.52 GHz and a remarkable absorption efficiency index of 35 dB· GHz mm-1. The maintained BN crystallinity, ordered sp2-carbon conversion, and enhanced interfacial compatibility between C-F-BN and polyvinyl alcohol (PVA) enable PVA/C-F-BN composites to attain higher through-plane thermal conductivity (0.2599 W·m-1·K-1) at a lower filler loading (5 wt.%). Moreover, the composite exhibits a broader absorption bandwidth of 3.84 GHz with a reflection loss of -32 dB. The design concept offers a feasible route to multifunctional materials for advanced electronic packaging.","PeriodicalId":228,"journal":{"name":"Small","volume":"31 1","pages":"e06851"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229123","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}
{"title":"Tailoring Surface Chemistry of Ti3C2Nx MXene for Superior H+, Li+, and Na+ Storage via Molten Salt-Derived N-Termination.","authors":"Tiezhu Guo,Wenfei Wei,Jiali Chai,Yuchuan Ren,Murat Yilmaz,Azim Uddin,Andreu Cabot,Di Zhou","doi":"10.1002/smll.202508556","DOIUrl":"https://doi.org/10.1002/smll.202508556","url":null,"abstract":"2D transition metal carbides and nitrides (MXene) are promising candidates for next-generation electrode materials due to their high electrical conductivity, large specific capacity/capacitance, and tunable surface chemistry. Nitrogen-doped MXene, in particular, have shown excellent electrochemical energy storage performance. However, the low and uneven nitrogen content has hindered both their performance and understanding of how N-terminal groups affect cation storage. This study successfully synthesizes N-terminated Ti3C2Nx via ion-exchange reactions in a hydrogen-containing argon atmosphere and investigates its energy storage behavior for H⁺, Li⁺, and Na⁺ ions. Ti3C2Nx shows outstanding H⁺ storage with a capacitance of 471 F g-1, while Li⁺ and Na⁺ storage exhibit a prominent intercalation mechanism. The Ti3C2Nx electrode delivers stable capacities of 209 mAh g-1 for Li⁺ and 79 mAh g-1 for Na⁺ after rate cycling, indicating good rate capability and reversibility. Combining density functional theory calculations with experimental data, this study reveals the correlations between adsorption energy, binding energy, and electronic density of states, highlighting the importance of real-gap distance in efficient cation intercalation, offering guidance for the design of MXene for H⁺, Li⁺, and Na⁺ storage.","PeriodicalId":228,"journal":{"name":"Small","volume":"20 1","pages":"e08556"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229145","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}
SmallPub Date : 2025-10-06DOI: 10.1002/smll.202508162
Yu-Ming Chen,Yu-Ching Chen,Kuang-Yuan Tu,Yi-Dong Lin,Yan-Gu Lin,Hsun-Yen Lin,Samiksha Bajaj,Jyh Ming Wu
{"title":"Piezocatalysis-Enabled High-Efficiency Hydrogen Evolution with Single-Atom Platinum on MoS2 Nanoflowers.","authors":"Yu-Ming Chen,Yu-Ching Chen,Kuang-Yuan Tu,Yi-Dong Lin,Yan-Gu Lin,Hsun-Yen Lin,Samiksha Bajaj,Jyh Ming Wu","doi":"10.1002/smll.202508162","DOIUrl":"https://doi.org/10.1002/smll.202508162","url":null,"abstract":"The advent of single-atom catalysts (SACs) has revolutionized catalysis, delivering outstanding performance in diverse chemical reactions. This study introduces a novel piezoelectric catalytic system employing single-atom platinum-modified MoS2 nanoflowers (NFs) for enhanced hydrogen evolution reactions (HER). High-angle annular dark field scanning transmission electron microscopy (HAADF-STEM) identifies single-atom platinum as bright dots, while X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) analyses verify its oxidation state and radial distance. Piezoresponse force microscopy (PFM) confirms increased piezoresponse amplitude due to structural asymmetry from platinum modification. Time-resolved photoluminescence (TRPL) reveals an extended carrier lifetime of 5.7 ns, while the modified catalyst (SA-Pt-01, MoS2 NFs with 1 wt.% Pt) achieves a fourfold increase in hydrogen production efficiency, reaching 2206.15 µmol·g-1·h-1. Notably, SA-Pt-1 generates 7786.9 µmol·g-1 in 12 h, showcasing sustained performance. Electron paramagnetic resonance (EPR) detects stronger •OH radical signals, indicating increased reactive availability. Density functional theory (DFT) simulations show that single-atom Pt incorporation enhances adsorption energy and reduces energy barriers for hydrogen production. These findings underscore the potential of single-atom Pt-modified MoS2 NFs as efficient, sustainable catalysts for clean hydrogen energy applications.","PeriodicalId":228,"journal":{"name":"Small","volume":"22 1","pages":"e08162"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229147","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}
SmallPub Date : 2025-10-06DOI: 10.1002/smll.202508106
Srinivasan Alagar,Hyunki Kim,Joonhee Moon,Jun Kim,Chandra Sekhar Rout,Han Seul Kim,Sang Mun Jeong
{"title":"Synergistic Effects of Cu(OH)2-CuO Anodes for Multiple-Step Energy Storage of Li-Ion Microbatteries.","authors":"Srinivasan Alagar,Hyunki Kim,Joonhee Moon,Jun Kim,Chandra Sekhar Rout,Han Seul Kim,Sang Mun Jeong","doi":"10.1002/smll.202508106","DOIUrl":"https://doi.org/10.1002/smll.202508106","url":null,"abstract":"Lithium-ion microbatteries (LIMBs) face challenges in achieving high power density without compromising energy density, due to limitations in assembly and kinetics. By overcoming LIMB electrode fabricated using a laser-assisted method, which significantly improves assembly precision and enhances reaction kinetics, the first anodization of Cu(OH)2-CuO nanoneedle hybrids on Cu foil for a LIB anode is reported. By resolving the limitations of previous metal-hydroxide electrodes associated with conventional conversion reactions, the novel anode achieves an unprecedently-high initial capacity of 3065 mAh g-1 which clearly exceeds the theoretical limit. X-ray Photoelectron Spectroscopy, Transmission Electron Microscopy, and in-situ Raman analysis revealed the nanoscale Cu-particles and LiOH in high-voltage reactions, alongside CuxHy, Li2O, and LiH in low-voltage hydride reactions. AIMD simulations additionally revealed the underlying atomistic mechanism. An in-plane LIMB using a laser-assisted method is further engineered, featuring in prelithiated Cu(OH)2-CuO as the anode and LiNi0.8Mn0.1Co0.1O2 as the cathode. This LIMB operates between 2.0 and 4.5 V, delivering a reversible capacity of 6.61 mAh cm-2 at 20 µA cm-2 and retaining over 83% capacity after 500 cycles. This work advances overall understanding of lithium storage and offers key insights for the design of next-generation LIMBs.","PeriodicalId":228,"journal":{"name":"Small","volume":"104 1","pages":"e08106"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229149","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}
{"title":"Engineering of Chain Extender Flexibility and Hierarchical Hydrogen Bonding Toward Ultra-Low-Temperature Poly(Urethane-Urea) Elastomers with Exceptional Toughness.","authors":"Kelei Luo,Xiaoyue Wang,Qian Dou,Pengrui Cao,Jing Yang,Lihe Guo,Qi Guo,Song Li,Qihua Wang,Tingmei Wang,Liming Tao","doi":"10.1002/smll.202509686","DOIUrl":"https://doi.org/10.1002/smll.202509686","url":null,"abstract":"The demand for elastomeric materials with exceptional mechanical properties at low temperatures is increasingly growing. However, meeting these requirements remains a significant challenge to date. The high strength and toughness of many PTMEG-based elastomers are compromised at low temperatures. The ordered nature of their molecular chains leads to (semi-)crystallization of the soft segments, preventing substantial recovery. In this study, a series of hydroxyl terminated polybutadiene-based polyurethane (HTPB-PU) elastomers (HPUs) with balanced rigidity and flexibility are synthesized by modulating the interplay between rigid (urethane and urea bonds combined with aryl groups) and flexible molecular segments (HTPB). Hierarchical hydrogen bonding and aryl π-π stacking form rigid nanostructured domains, together with the large polarity difference and absence of hydrogen bonds between the soft and hard segments of HPUs, resulting in pronounced microphase separation. The rigid nanostructured domains disrupt the regular alignment of HTPB chains, thereby enabling the material to maintain exceptional ductility at -70 °C. Consequently, the HPUs exhibit remarkable elongation at break (842.6 ± 7.4%), exceptional fracture toughness (254.1 ± 16.0 MJ m-3), as well as excellent tear resistance, oil resistance, solvent resistance, and fatigue resistance at -70 °C. These findings provide a promising pathway for designing next-generation elastomers for extreme environments.","PeriodicalId":228,"journal":{"name":"Small","volume":"47 1","pages":"e09686"},"PeriodicalIF":13.3,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229150","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}