Runqiu Liu, Zhifan Song, Xi Wang, Jiangyan Wang, Jingsong Wang, Dan Wang, Ranbo Yu
{"title":"Progress and Perspectives on Confinement Engineering to Revive Alloying‐Type Anode Materials for Sodium‐Ion Batteries","authors":"Runqiu Liu, Zhifan Song, Xi Wang, Jiangyan Wang, Jingsong Wang, Dan Wang, Ranbo Yu","doi":"10.1002/smll.76046","DOIUrl":"https://doi.org/10.1002/smll.76046","url":null,"abstract":"With the rise of sodium‐ion batteries (SIBs), alloying‐type anodes offer high specific capacities and suitable operating potentials through multi‐electron reactions, positioning them as key to enhancing the energy density of SIBs. However, their serious volume expansion leads to electrode pulverization and repeated rupture of the solid electrolyte interphase (SEI) film, severely compromising the cycle life. Confinement engineering has recently emerged as a powerful strategy for addressing the intrinsic limitations of alloying‐type anodes. Nevertheless, systematic classification and in‐depth mechanism clarification of diverse confinement strategies remain lacking. To fill this gap, this review systematically summarizes the fundamental principles, structural motifs, and design strategies of confinement engineering. Different from previous material‐oriented reviews, this work categorizes confinement engineering into self‐confinement and extrinsic confinement, and profoundly clarifies the structure‐regulation mechanism at the micro/nano scale, emphasizing the critical role of confinement engineering in mitigating volume expansion, stabilizing SEI films, and enhancing reaction kinetics. Key advances in alloying‐type anode development are highlighted, alongside a critical assessment of the persisting challenges. Finally, future directions are outlined to provide theoretical guidance and innovative strategies for accelerating the commercialization of alloying‐type anode materials for high‐energy‐density and long‐cycle‐life SIBs.","PeriodicalId":228,"journal":{"name":"Small","volume":"19 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172955","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":"Low‐Energy Vertical Organic Synaptic Transistors Enabled by Siloxane Crosslinking‐Induced Edge‐On Molecular Ordering","authors":"Jiale Huang, Linfeng Lan, Yutian Liu, Bo Huang, Ruibin Liang, Shuguang Zhang, Junbiao Peng","doi":"10.1002/smll.76273","DOIUrl":"https://doi.org/10.1002/smll.76273","url":null,"abstract":"The von Neumann bottleneck has driven the development of low‐power neuromorphic devices such as vertical organic synaptic transistors (VOSTs), which offer ultrashort charge transport pathways and high integration density. However, their performance is still limited by poor molecular ordering and the difficulty in achieving effective gate‐controlled modulation. Here, a siloxane crosslinking strategy is proposed by incorporating 1,6‐bis(trichlorosilyl)hexane (C6Si) into poly(3‐hexylthiophene) (P3HT) to form a dense cross‐linked network, enabling improved molecular ordering, backbone planarity, and interfacial stability. As a result, a pronounced edge‐on molecular orientation of 93.00% was achieved, establishing efficient vertical charge transport pathways. The ion gel‐gated VOSTs exhibited excellent electrical performance at an ultralow operation voltage (−0.5 V), including high on/off current ratio ( <jats:italic>I</jats:italic> <jats:sub>on</jats:sub> / <jats:italic>I</jats:italic> <jats:sub>off</jats:sub> ) (9.48 × 10 <jats:sup>4</jats:sup> ), low subthreshold swing ( <jats:italic>SS</jats:italic> ) (111 mV dec <jats:sup>−1</jats:sup> ), and the minimum synaptic‐event energy consumption at low level (∼50 aJ), along with rich synaptic plasticity. Ex‐situ neural network simulations demonstrate over 91% accuracy in MNIST handwritten digit recognition. Meanwhile, the device arrays enable high‐contrast image reconstruction and visual memory functions, providing an effective molecular design strategy for the development of low‐cost, scalable neuromorphic computing devices.","PeriodicalId":228,"journal":{"name":"Small","volume":"53 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172956","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}
Prakash Govindaraj, M. V. Jyothirmai, Kathirvel Venugopal, Rajkamal Anand, Hern Kim
{"title":"CO 2 Capture in MOFs: Connecting Experiments, Multiscale Simulations, and Data‐Driven Approaches","authors":"Prakash Govindaraj, M. V. Jyothirmai, Kathirvel Venugopal, Rajkamal Anand, Hern Kim","doi":"10.1002/smll.76202","DOIUrl":"https://doi.org/10.1002/smll.76202","url":null,"abstract":"Metal–organic frameworks (MOFs) have emerged as promising porous materials for CO <jats:sub>2</jats:sub> capture due to their tunable pore structures and chemically versatile adsorption sites. However, achieving efficient capture at low CO <jats:sub>2</jats:sub> concentrations while balancing adsorption strength, regeneration, and structural stability remains challenging. Existing reviews often treat experimental and computational investigations separately, limiting the development of unified design principles. This review integrates experimental insights with multiscale computational approaches, including density functional theory (DFT), grand canonical Monte Carlo, molecular dynamics, and computational fluid dynamics (CFD). DFT calculations provide molecular‐level understanding of adsorption behavior, highlighting the role of electronic structure at open metal sites and functionalized pores. Classical simulations predict adsorption capacity, selectivity, and diffusion, while CFD extends these insights to macroscopic transport and process‐level performance, enabling direct comparison with experiments. In addition, emerging data‐driven approaches are discussed to uncover structure–property relationships and accelerate performance prediction across large materials spaces. The integration of these methods establishes a closed‐loop framework linking theory, simulation, and experiment, guiding the rational design of efficient and stable porous materials for practical CO <jats:sub>2</jats:sub> capture applications.","PeriodicalId":228,"journal":{"name":"Small","volume":"1 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172957","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}
Shuhan He, Xin Wang, Si Li, Hengwei Lin, Jianping Yang
{"title":"Directing Neuronal Differentiation via Calcium‐Chirality Synergy in Supramolecular Nanofibers","authors":"Shuhan He, Xin Wang, Si Li, Hengwei Lin, Jianping Yang","doi":"10.1002/smll.76276","DOIUrl":"https://doi.org/10.1002/smll.76276","url":null,"abstract":"While chiral supramolecular nanofibrous networks (NFNs) show promise in regulating cell fate, precisely directing differentiation pathways remains challenging. This study systematically investigates the influence of various chiral supramolecular NFNs on neural cell differentiation. A series of chiral supramolecular NFNs was synthesized using L/D‐amino acids and their derivatives as building blocks, including L/D‐lysine (L/D‐Lys), L/D‐histidine (L/D‐His), L/D‐arginine (L/D‐Arg), and L/D‐glutamic acid derivatives (Fmoc‐L/D‐Glu). The regulatory effects of these NFNs on the NG108‐15 were evaluated during the differentiation process. Our findings demonstrate that the chiral microenvironment established by D‐Lys‐gel significantly enhances NG108‐15 differentiation and correlates with robust activation of the Ca <jats:sup>2+</jats:sup> signaling pathway. To further elucidate the relationship between supramolecular chirality and metal ions, we synthesized chiral supramolecular NFNs from L/D‐Lys‐Ca <jats:sup>2+</jats:sup> ‐gel and L/D‐Lys‐Mg <jats:sup>2+</jats:sup> ‐gel. Notably, the supramolecular NFNs derived from D‐Lys‐Ca <jats:sup>2+</jats:sup> ‐gel exhibited superior capacity to promote neurite outgrowth and maturation compared to their L‐enantiomer and Mg <jats:sup>2+</jats:sup> ‐incorporated counterparts. Proteomics analysis revealed that the chiral supramolecular NFNs obtained from D‐Lys‐Ca <jats:sup>2+</jats:sup> ‐gel enhance neuronal differentiation by upregulating key effectors involved in both axon guidance and calcium signaling pathways, particularly the Camkk2‐Tiam1 cascade. This study provides valuable insights into the design of chiral biomaterials and proposes novel strategies for neural regeneration and tissue engineering.","PeriodicalId":228,"journal":{"name":"Small","volume":"15 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172680","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}
Huawei Liu, Shengming Wu, Han Zhou, Ming Yin, Chenlong He, Hongyi Zhang, Shan Hua, Keyue Xiao, YuAn Zhu, Haiying Ji, Yilong Wang
{"title":"A Nanodelivery Platform Harnessing Synthetic Lethality and Efferocytosis Inhibition for Synergistically Enhanced Immunotherapy of Triple‐Negative Breast Cancer","authors":"Huawei Liu, Shengming Wu, Han Zhou, Ming Yin, Chenlong He, Hongyi Zhang, Shan Hua, Keyue Xiao, YuAn Zhu, Haiying Ji, Yilong Wang","doi":"10.1002/smll.76306","DOIUrl":"https://doi.org/10.1002/smll.76306","url":null,"abstract":"Triple‐negative breast cancer (TNBC), defined by the absence of specific therapeutic targets, shows poor clinical benefit and readily develops chemoresistance, underscoring the need for therapies that couple precise tumor cell killing with robust antitumor immunity. Drug‐induced immunogenic cell death (ICD) is a promising approach. However, its efficacy is curtailed by limited tumor‐cell targeting with collateral immune‐cell damage and by overactive efferocytosis that rapidly removes ICD‐associated danger signals, thereby restricting antitumor immunity. Herein, we develop a microenvironment‐responsive nanocarrier co‐delivering both PLK1 inhibitor (BI6727) and TIM‐3 inhibitor (ML‐T7). It integrates dual‐bioeffect of synthetic lethal selective ICD and whole‐immuno system remodelling initiated by effective macrophage efferocytosis inhibition. In detail, the molecular hallmark differences between tumor and immune cells was utilized to provide high‐quality antigens. Meanwhile, the nanotherapeutic enables serial phagocyte regulations, such as, suppressed macrophage phagocytosis, enhanced antigen recognition and phagocytosis by dendritic cells (DCs), and then alleviated T cell exhaustion. The underlying mechanism of nanotherapeutics‐mediated overall immune system reprogramming was explored by transcriptional profile analyses. These findings indicate that precise molecularly targeted ICD combined with coordinated immune activation enables efficient primary tumor suppression and promotes T‐cell phenotypes associated with antitumor immune memory, providing a novel paradigm for cancer immunotherapy.","PeriodicalId":228,"journal":{"name":"Small","volume":"19 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172687","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}
Xiaoli Ran, Feihong Ke, Wenzheng Yang, Yanlong Gong, Haitao Fu, Xizhong An, Dawei Su, Xiaohong Yang
{"title":"Spatially Programmable S‐Scheme Heterojunction Photoanodes via Aerosol‐Jet Printing for Efficient Solar Water Oxidation","authors":"Xiaoli Ran, Feihong Ke, Wenzheng Yang, Yanlong Gong, Haitao Fu, Xizhong An, Dawei Su, Xiaohong Yang","doi":"10.1002/smll.76307","DOIUrl":"https://doi.org/10.1002/smll.76307","url":null,"abstract":"S‐scheme heterojunctions enable efficient charge separation while preserving the strong redox ability of photogenerated carriers, offering a powerful platform for advanced photoelectrochemical (PEC) water splitting. However, translating such rationally designed heterostructures into scalable, high‐performance photoanodes remains a critical bottleneck for conventional fabrication methods. Here, we develop an aerosol‐jet printing (AJP) approach to fabricate S‐scheme SrTiO <jats:sub>3</jats:sub> /g‐C <jats:sub>3</jats:sub> N <jats:sub>4</jats:sub> heterojunction photoanodes with well‐controlled stacking sequences. The interfacial built‑in electric field drives recombination of SrTiO <jats:sub>3</jats:sub> photogenerated electrons with g‑C <jats:sub>3</jats:sub> N <jats:sub>4</jats:sub> holes, preserving the strongly oxidizing holes in SrTiO <jats:sub>3</jats:sub> for the oxygen evolution reaction (OER). The SrTiO <jats:sub>3</jats:sub> ‐on‐C <jats:sub>3</jats:sub> N <jats:sub>4</jats:sub> configuration delivers enhanced PEC water oxidation activity, with a photocurrent density of 2.3 mA cm <jats:sup>−</jats:sup> <jats:sup>2</jats:sup> , double that of single‐component and reversed‐structure photoanodes. It is found that this enhancement stems from stacking‐order‐dependent synergy between the heterojunction built‐in electric field and semiconductor‐electrolyte band bending. Notably, AJP enables fabrication of large‐area, module‐sized photoanodes, demonstrating practical scalability for device manufacturing. This work provides a controllable, scalable route for the rational design of high‐performance S‐scheme heterojunction photoelectrodes for PEC water splitting.","PeriodicalId":228,"journal":{"name":"Small","volume":"82 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172688","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":"Piezoelectric and Dielectric Enhancement in Orientation‐Engineered Freestanding Epitaxial Ba(Ti,Sn)O 3 Membranes","authors":"Pranab Kumar Roy, Soumen Pradhan, Harsh Joshi, Gurukrishna K, Fabian Hartmann, Sven Höfling, Ashish Garg, Shikhar Misra","doi":"10.1002/smll.76272","DOIUrl":"https://doi.org/10.1002/smll.76272","url":null,"abstract":"Heterogeneous integration of freestanding single‐crystalline ferroelectric membranes offers a promising route to leverage their dielectric, piezoelectric, and nonlinear optical behavior in adaptive electronics. Crystallographic orientation engineering in these membranes further enables tuning of strain states, domain characteristics, and resulting functional properties. While orientation‐engineered Pb‐based piezoelectric membranes have been demonstrated, similar studies on Pb‐free systems remain limited. Here, single‐crystalline BaTi <jats:sub>0.97</jats:sub> Sn <jats:sub>0.03</jats:sub> O <jats:sub>3</jats:sub> (BST) membranes along three different crystallographic orientations are fabricated via an epitaxial layer lift‐off process on Indium Tin oxide (ITO)‐coated glass substrates to investigate the anisotropic dielectric, piezoelectric, and ferroelectric properties. Relaxation of substrate‐induced compressive strain promotes enhanced in‐plane and out‐of‐plane domain nucleation, yielding superior piezoelectric and dielectric responses across all orientations. An enhanced piezoelectric response in all BST membranes (61–113 pm/V) is observed. Dielectric analysis further reveals a significant enhancement in permittivity for all the freestanding membranes compared to their clamped counterparts, at frequencies above ∼10 <jats:sup>5</jats:sup> Hz (∼150 at 5 MHz), indicating faster polarization relaxation dynamics. Overall, this study demonstrates the influence of crystallographic orientation on domain evolution in freestanding membranes and paves the way for their integration into next‐generation high‐frequency dielectric and microelectromechanical devices.","PeriodicalId":228,"journal":{"name":"Small","volume":"188 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172694","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}
Longfeng Zou, Yucheng Jiang, Taoying Rao, Siying He, Long Teng, Yilan Guo, Pengli Zhu, Yimin Yao
{"title":"Conversion‐Controlled Poly(Ionic Liquid)/Aluminum Nitride Thermal Interface Materials with Internal Plasticization for Reliable Chip‐Level Thermal Management","authors":"Longfeng Zou, Yucheng Jiang, Taoying Rao, Siying He, Long Teng, Yilan Guo, Pengli Zhu, Yimin Yao","doi":"10.1002/smll.76290","DOIUrl":"https://doi.org/10.1002/smll.76290","url":null,"abstract":"The increasing power densities of artificial intelligence and high‐performance computing (HPC) chips place stringent demands on thermal interface materials (TIMs), which are designed to combine efficient heat transport with interfacial conformability, stress relaxation, and long‐term reliability. Conventional silicone‐based TIMs can suffer from oil bleeding, pump‐out, and insufficient adhesion during prolonged thermal exposure. Here, a conversion‐controlled poly(ionic liquid)/aluminum nitride (PIL/AlN) thermal gel is developed by partially polymerizing the PIL matrix. The resulting chain‐entangled PIL framework retains residual monomer and oligomer species that provide internal plasticization, promote interfacial wetting, and facilitate stress relaxation, while densely packed spherical AlN particles establish heat‐transfer pathways. After optimization of polymerization time and filler loading, the 55 vol% AlN composite exhibits an elongation‐at‐break of 291%, adhesion strengths of 5.4 MPa on Cu and 3.7 MPa on Si, and a bulk thermal conductivity of 2.0 W·m <jats:sup>−1</jats:sup> ·K <jats:sup>−1</jats:sup> . Its mechanical compliance enables intimate contact with Si, yielding an interfacial thermal resistance of (2.93 ± 0.96) × 10 <jats:sup>−6</jats:sup> K·m <jats:sup>2</jats:sup> ·W <jats:sup>−1</jats:sup> . T3Ster cycling and high‐temperature aging further show stable device‐level thermal responses and no detectable macroscopic defects under the tested conditions. This conversion‐controlled strategy provides a route to silicone‐free TIMs that combine mechanical compliance, interfacial adhesion, low interfacial thermal resistance, and operational stability.","PeriodicalId":228,"journal":{"name":"Small","volume":"5 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172686","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":"Correction to “Can Entropically Unfavorable Topological Hydrogen‐Bonded Networks Form from Tetrakis‐ or Pentakis(4‐carboxyphenyl)‐benzene Derivative?”","authors":"","doi":"10.1002/smll.76031","DOIUrl":"https://doi.org/10.1002/smll.76031","url":null,"abstract":"","PeriodicalId":228,"journal":{"name":"Small","volume":"33 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172689","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}
Carice Chong, Siew Kheng Boong, Tharishinny Raja Mogan, Jiajia Zhang, Hongjian Yu, Yue‐e Miao, Hiang Kwee Lee
{"title":"Structure‐Dependent Interfacial Electrostatic Regulation Enables Platinum‐Efficient Hydrogen Evolution in Pt‐Ag Bimetallic Nanowires","authors":"Carice Chong, Siew Kheng Boong, Tharishinny Raja Mogan, Jiajia Zhang, Hongjian Yu, Yue‐e Miao, Hiang Kwee Lee","doi":"10.1002/smll.76263","DOIUrl":"https://doi.org/10.1002/smll.76263","url":null,"abstract":"The electrocatalytic hydrogen evolution reaction (HER) is central to sustainable hydrogen production. Platinum (Pt) is widely regarded as the benchmark HER catalyst due to its near‐optimal catalytic properties. However, its scarcity and high cost severely constrain scalable deployment. Here, we demonstrate that structure‐induced interfacial electrostatic regulation enables platinum‐efficient HER while minimizing Pt loading. A one‐dimensional nanoensemble composed of Ag nanowires decorated with Pt nanoparticles integrates electronic hybridization, facet‐dependent charge accumulation, and directional charge transport to boost HER. The solid PtAgNW (S‐PtAgNW) nanoarchitecture containing only 15 wt.% Pt achieves the lowest overpotential of 290 mV at an ECSA‐normalized current density of 500 mA cm <jats:sup>−2</jats:sup> with a Tafel slope of 42 mV dec <jats:sup>−1</jats:sup> . It delivers a Pt‐normalized hydrogen production rate of ∼50 mol g <jats:sub>Pt</jats:sub> <jats:sup>−1</jats:sup> h <jats:sup>−1</jats:sup> at ∼93% Faradaic efficiency, representing a >6‐fold enhancement over its hollow counterpart despite the latter possessing higher Pt loading and similar interfacial chemistry. Mechanistic analysis reveals that Ag‐to‐Pt electronic coupling and facet redistribution toward Ag(111) enhance electron accumulation under bias, strengthening the interfacial electrostatic environment that governs proton‐electron coupling. These findings establish interfacial electrostatic regulation, rather than Pt loading or intrinsic catalyst chemistry alone, as an important determinant of efficient HER.","PeriodicalId":228,"journal":{"name":"Small","volume":"77 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149172692","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}