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Polymer‐Coordinated Heterogeneous Zeolitic Imidazolate Framework‐8 with Exceptional Propylene/Propane Molecular Sieving Effect 聚合物-配位非均相咪唑酸分子筛- 8具有特殊的丙烯/丙烷分子筛分效果
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-26 DOI: 10.1002/smll.202505746
Sunghwan Park, Ho Jin Jung, Se Hun Kim, Hoang Vu Ly, Seung‐Soo Kim, Dong A. Kang, Young Je Kwon, Seunghyeon Joo, Kie Yong Cho, Hae‐Kwon Jeong
{"title":"Polymer‐Coordinated Heterogeneous Zeolitic Imidazolate Framework‐8 with Exceptional Propylene/Propane Molecular Sieving Effect","authors":"Sunghwan Park, Ho Jin Jung, Se Hun Kim, Hoang Vu Ly, Seung‐Soo Kim, Dong A. Kang, Young Je Kwon, Seunghyeon Joo, Kie Yong Cho, Hae‐Kwon Jeong","doi":"10.1002/smll.202505746","DOIUrl":"https://doi.org/10.1002/smll.202505746","url":null,"abstract":"Zeolitic imidazolate framework‐8 (ZIF‐8) is a promising material for C<jats:sub>3</jats:sub>H<jats:sub>6</jats:sub>/C<jats:sub>3</jats:sub>H<jats:sub>8</jats:sub> separation; however, its inherent linker flexibility compromises molecular sieving effect. To address this limitation, a novel ZIF‐8, namely heterogeneous ZIF‐8 (hZIF‐8), is developed, consisting of nanocrystalline ZIF‐8 phases with a minor amorphous polymer component introduced via in situ coordination. hZIF‐8 is synthesized through a Lewis‐acid‐catalyzed cationic ring‐opening polymerization of tetrahydrofuran (THF), generating polytetramethylene ether glycol (PTMEG) chains that competitively coordinate with zinc ions during ZIF‐8 crystallization. This coordination‐mediated heterogeneous structure exhibits unique characteristics distinct from conventional ZIF‐8 and other polymer hybrid MOFs such as PolyMOFs. The polymer phase effectively restricts the linker flexibility of the nanocrystalline phase at the molecular level, leading to significantly enhanced molecular sieving properties. As a result, hZIF‐8‐containing mixed‐matrix membranes (MMMs) exhibit a significant enhancement in C<jats:sub>3</jats:sub>H<jats:sub>6</jats:sub>/C<jats:sub>3</jats:sub>H<jats:sub>8</jats:sub> separation performance, with the separation factor increasing from 13.3 to 75.5 (by 468%) and the C<jats:sub>3</jats:sub>H<jats:sub>6</jats:sub> permeability from 7.4 to 17.4 Barrer (by 135%) at 30 wt.% loading. Furthermore, the intrinsic selectivity of hZIF‐8 is predicted to reach ≈3700, representing an order‐of‐magnitude improvement over that of pristine ZIF‐8 (≈180).","PeriodicalId":228,"journal":{"name":"Small","volume":"116 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2025-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144710663","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
Efficient Ta3N5 Photoanodes via Interface Engineering of Bixbyite‐Type Ta2N3 Precursors Bixbyite型Ta2N3前驱体的界面工程制备高效Ta3N5光阳极
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-26 DOI: 10.1002/smll.202505487
Chia‐Wei Chang, Bo‐Ying Lai, Chang‐Ming Jiang
{"title":"Efficient Ta3N5 Photoanodes via Interface Engineering of Bixbyite‐Type Ta2N3 Precursors","authors":"Chia‐Wei Chang, Bo‐Ying Lai, Chang‐Ming Jiang","doi":"10.1002/smll.202505487","DOIUrl":"https://doi.org/10.1002/smll.202505487","url":null,"abstract":"Tantalum nitride (Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub>) shows promising prospects for photoelectrochemical (PEC) water splitting due to its suitable band gap and band edge positions. However, high‐performing Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub> photoanodes typically require Ta foil substrates and film thicknesses of several hundred nanometers, leading to increased tantalum usage and fabrication costs. This study introduces bixbyite‐type Ta<jats:sub>2</jats:sub>N<jats:sub>3</jats:sub> as a superior precursor for synthesizing thin (≈100 nm) Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub> films on silicon substrates, substantially reducing tantalum consumption while maintaining excellent PEC performance. The metastable Ta<jats:sub>2</jats:sub>N<jats:sub>3</jats:sub> phase undergoes disproportionation into Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub> and conductive Ta‐subnitrides during ammonolysis, enabling efficient charge separation without relying on Ta foils. Optimization of ammonolysis conditions reveals a critical balance between Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub> crystallinity, subnitride content, and surface Ta<jats:sup>3+</jats:sup> defect concentrations. Furthermore, degenerately doped silicon substrates enhance hole extraction by suppressing charge accumulation and leakage at the Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub>/Si junction, as revealed by photoelectrochemical impedance spectroscopy. This synthesis strategy yields an anodic photocurrent density of 3.86 mA cm<jats:sup>−2</jats:sup> at 1.23 V<jats:sub>RHE</jats:sub> for a 100 nm Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub> film on n<jats:sup>+</jats:sup>‐Si(111), outperforming a 500 nm film derived from TaO<jats:sub>x</jats:sub> precursor and achieving a 0.15 V cathodic shift in onset potential. These findings establish a scalable, low‐Ta usage platform for advancing Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub>‐based PEC systems in solar fuel technologies.","PeriodicalId":228,"journal":{"name":"Small","volume":"707 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2025-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144710664","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
The Challenges and Opportunities of Protein Coronas for Nanoscale Biomolecular Sensing 蛋白质冠状体用于纳米生物分子传感的挑战与机遇
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-26 DOI: 10.1002/smll.202503820
Samuel Cheeseman, Parisa Moazzam, Negar Mahmoudi, Morteza Mahmoudi, Frank Caruso, Antonio Tricoli, David R. Nisbet
{"title":"The Challenges and Opportunities of Protein Coronas for Nanoscale Biomolecular Sensing","authors":"Samuel Cheeseman, Parisa Moazzam, Negar Mahmoudi, Morteza Mahmoudi, Frank Caruso, Antonio Tricoli, David R. Nisbet","doi":"10.1002/smll.202503820","DOIUrl":"https://doi.org/10.1002/smll.202503820","url":null,"abstract":"The unique benefits of sub‐picomolar and single‐molecule detection for the diagnosis and prognosis of diseases and therapeutic efficacy monitoring have been driving the development of nanoscale biomolecular sensors. Nanoscale sensors can be attached to the surface or dispersed in solution, enabling the rapid detection of analytes with high sensitivity and specificity by overcoming concentration‐driven diffusion limits. In biological fluids, however, nanoscale objects are surrounded by biomolecules, mostly proteins, that form an evolving encapsulating surface layer, commonly known as the protein corona. The protein corona can modify the biosensor surface, which can adversely impact biosensing specificity, sensitivity, and accuracy. Conversely, the protein corona can be exploited to design biosensors for disease diagnostics, the discovery of new biomarkers, and environmental contaminants. In this review, the factors influencing protein corona formation on nanoscale biosensors are examined. Characterization methods and the effects of protein corona formation on the performance of nanoscale biosensors are also discussed. Promising strategies to prevent, circumvent, and exploit corona formation are presented and this review concludes by outlining future perspectives of nanoscale biomolecular sensors for practical application in biological fluids.","PeriodicalId":228,"journal":{"name":"Small","volume":"57 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2025-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144710666","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
Hydrogen Production from Catalytic Steam Reforming of Bio-Oil: Recent Advances in Coke Resistance. 生物油催化蒸汽重整制氢:抗焦性研究进展。
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-25 DOI: 10.1002/smll.202505296
Xin Li,Ping Zou,Xiang Zhu,Sheng Dai,Xia Jiang
{"title":"Hydrogen Production from Catalytic Steam Reforming of Bio-Oil: Recent Advances in Coke Resistance.","authors":"Xin Li,Ping Zou,Xiang Zhu,Sheng Dai,Xia Jiang","doi":"10.1002/smll.202505296","DOIUrl":"https://doi.org/10.1002/smll.202505296","url":null,"abstract":"Catalytic steam reforming of bio-oil has emerged as an efficient, environmentally friendly, and economic approach for the production of green hydrogen, which is of great interest as a promising energy carrier in renewable energy systems, owing to its high energy density and zero-pollution emission. However, the steam reforming performance, in terms of hydrogen yield and catalytic stability, has been severely affected by catalyst deactivation due to the inevitable coke formation. This review offers a comprehensive overview of the mechanism of bio-oil steam reforming and the formation of carbonaceous deposits, accompanied with their compositions and locations. Most importantly, recent advances made in the development of coke-resistant steam reforming catalysts have been carefully discussed, with an emphasis on alleviation strategies toward the inhibition of coke formation and enhancement in hydrogen production, thereby affording deeper insights of the structure-function relationships. The challenges and future prospects are further discussed.","PeriodicalId":228,"journal":{"name":"Small","volume":"9 1","pages":"e05296"},"PeriodicalIF":13.3,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144701135","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
CdIn2S4 Micro-Pyramids for Reductive Photocatalytic Degradation of Perfluorooctanesulfonic Acid. 全氟辛烷磺酸还原性光催化降解CdIn2S4微金字塔。
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-25 DOI: 10.1002/smll.202504601
Mahmoud Adel Hamza,Alexander James Keltie,Rachael Kate Matthews,Mabel Lily Day,Cameron James Shearer
{"title":"CdIn2S4 Micro-Pyramids for Reductive Photocatalytic Degradation of Perfluorooctanesulfonic Acid.","authors":"Mahmoud Adel Hamza,Alexander James Keltie,Rachael Kate Matthews,Mabel Lily Day,Cameron James Shearer","doi":"10.1002/smll.202504601","DOIUrl":"https://doi.org/10.1002/smll.202504601","url":null,"abstract":"Per- and poly-fluoroalkyl substances (PFAS) constitute a class of persistent organic pollutants that severely affect human health and the environment owing to their resistance to degradation by traditional water treatment methods. Semiconductor-assisted photocatalysis has the potential to be a green method to achieve complete mineralization of PFAS. Cadmium indium sulfide (CdIn2S4) is an exciting photocatalytic material because of its high visible light harvesting capacity and high reduction potential. However, CdIn2S4 has not been investigated for PFAS degradation. Herein, CdIn2S4 micro-pyramids are fabricated via solvothermal synthesis, and their photocatalytic activity toward the photodegradation of perfluorooctanesulfonic acid (PFOS) is investigated. The reaction conditions, such as the light source and the light power are optimized. The findings show the capability of CdIn2S4 to achieve almost complete degradation and defluorination of PFOS (removal% = 99 ± 7% and defluorination% = 97 ± 22%) under optimized conditions. From radical quenching experiments, it is found that the mechanism of degradation is via photoelectron reduction. CdIn2S4 shows an outstanding performance toward the degradation of the PFAS sample derived from a contaminated facility in South Australia. This work opens the door for investigating other CdIn2S4-based photocatalysts and other metal sulfide-based photocatalysts for the degradation of PFAS.","PeriodicalId":228,"journal":{"name":"Small","volume":"115 1","pages":"e04601"},"PeriodicalIF":13.3,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144701140","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
Potential Applications of Multifunctional Tetrahedral Framework Nucleic Acids in Bone Tissue Engineering. 多功能四面体框架核酸在骨组织工程中的潜在应用。
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-25 DOI: 10.1002/smll.202411930
Wen Tang,Weitong Lu,Sirong Shi,Yunfeng Lin
{"title":"Potential Applications of Multifunctional Tetrahedral Framework Nucleic Acids in Bone Tissue Engineering.","authors":"Wen Tang,Weitong Lu,Sirong Shi,Yunfeng Lin","doi":"10.1002/smll.202411930","DOIUrl":"https://doi.org/10.1002/smll.202411930","url":null,"abstract":"Though bone defects are common, treating critical-sized bone defects remains a significant clinical challenge. A potential strategy for bone repair that avoids the need for autogenous bone grafts is bone tissue engineering (BTE). Recently, BTE strategies incorporating vascularization, neurorestoration, and immunomodulation of bone substitutes are regarded as a comprehensive and promising method for bone repair. Despite advancements, existing approaches struggle to achieve overall bone regeneration. Emerging DNA nanotechnology, specifically tetrahedral framework nucleic acids (tFNAs), presents a transformative approach due to their rapid self-assembly, structural stability, efficient cellular uptake, multiple biological activities, and excellent biocompatibility. tFNAs allow for flexible modifications with various bioactive molecules, including oligonucleotides, peptides, and small molecular drugs, thus strengthening their targeting and therapeutic abilities. tFNAs can enhance osteogenesis by promoting mesenchymal stem cell viability and differentiation, thereby stimulating bone formation. Furthermore, tFNAs integrated with scaffolds contribute to the development of advanced biomaterials with superior osteoinductive properties. tFNAs also influence angiogenesis, neurorestoration, and immunomodulation, all of which are crucial for bone repair. This review not only examines the potential applications of multifunctional tFNAs in BTE but also provides critical insights into the advantages, challenges, and prospects of tFNAs in BTE.","PeriodicalId":228,"journal":{"name":"Small","volume":"18 1","pages":"e2411930"},"PeriodicalIF":13.3,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144701057","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
Efficient Inverted Perovskite Solar Cells Utilizing Inorganic Composite Multiple Electron Transport Layers. 利用无机复合多电子传输层的高效倒置钙钛矿太阳能电池。
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-25 DOI: 10.1002/smll.202411978
Annan Zhu,Hao Gu,Wang Li,Jia Guo,Shengwen Li,Gang Wang,Junmin Xia,Chao Liang,Shi Chen,Guichuan Xing
{"title":"Efficient Inverted Perovskite Solar Cells Utilizing Inorganic Composite Multiple Electron Transport Layers.","authors":"Annan Zhu,Hao Gu,Wang Li,Jia Guo,Shengwen Li,Gang Wang,Junmin Xia,Chao Liang,Shi Chen,Guichuan Xing","doi":"10.1002/smll.202411978","DOIUrl":"https://doi.org/10.1002/smll.202411978","url":null,"abstract":"Electron transport layers (ETLs) featuring optimal film coverage and favorable electronic properties play a critical role in high-performance perovskite solar cells (PSCs). In contrast to organic ETLs, which have high material costs, inorganic metal oxide ETLs are considered promising alternatives for efficient inverted PSCs because of their low cost, high carrier mobility, and excellent stability. However, fabricating high-quality top inorganic ETLs that preserve the active perovskite layer remains a challenge. Herein, a composite electron transport bilayer comprising atomically coherent interfaced tin dioxide (SnO2) nanoparticles and tungsten-doped zinc oxide (WZO) is introduced, which further facilitates charge extraction and mitigates detrimental interfacial deprotonation reactions. The tungsten doping ratio can be precisely controlled by adjusting the co-evaporation parameters. The results reveal that tungsten enhances charge extraction by fine-tuning the energy levels, whereas the SnO2 layer simultaneously passivates the perovskite/ETL interface defects and inhibits deprotonation reactions. Utilizing this inorganic composite multiple architecture, a record efficiency of 23.19% is achieved for inverted PSCs with an all-inorganic ETL. This cost-effective approach provides a viable pathway for industrial-scale production of high-performance PSCs.","PeriodicalId":228,"journal":{"name":"Small","volume":"56 1","pages":"e11978"},"PeriodicalIF":13.3,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144701134","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
Advanced Textile-Based Lithium-Metal Batteries: Interfacial Engineering, Structural Design, and Wearable Applications. 先进的纺织基锂金属电池:界面工程、结构设计和可穿戴应用。
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-25 DOI: 10.1002/smll.202506422
Shengchen Yang,Dongdong Li
{"title":"Advanced Textile-Based Lithium-Metal Batteries: Interfacial Engineering, Structural Design, and Wearable Applications.","authors":"Shengchen Yang,Dongdong Li","doi":"10.1002/smll.202506422","DOIUrl":"https://doi.org/10.1002/smll.202506422","url":null,"abstract":"Textile-based lithium-metal batteries (TLMBs), pivotal for next-generation wearable energy storage, offer unparalleled advantages including ultrahigh theoretical capacity (3860 mAh g⁻¹), low electrochemical potential (-3.04 V vs standard hydrogen electrode), and seamless integration with flexible electronics. However, critical challenges such as dendritic lithium growth, unstable solid-electrolyte interphase (SEI) evolution, and mechanical degradation under dynamic deformation hinder their practical deployment. This review presents a transformative paradigm centered on hierarchical structural engineering-encompassing atomic-to-macroscale interfacial design and textile-architecture optimization-to address these barriers. The roles of gradient-pore distributions, Janus-structured fibers, and kirigami-inspired geometries are systematically dissected in homogenizing Li-ion flux, stabilizing SEI layers, and decoupling mechanical stress from electrochemical pathways, enabling TLMBs to sustain >500% strain without capacity loss. Furthermore, system-level integration strategies for self-powered health-monitoring textiles and thermally adaptive batteries are scrutinized, bridging fundamental insights with scalable manufacturing. By identifying underexplored frontiers such as dynamic SEI regulators and circular economy-aligned designs, this work provides a strategic roadmap to advance TLMBs toward high-energy, mechanically robust wearable systems. The analysis aims to inspire interdisciplinary innovation, accelerating the transition from lab-scale breakthroughs to real-world applications in flexible energy storage.","PeriodicalId":228,"journal":{"name":"Small","volume":"22 1","pages":"e06422"},"PeriodicalIF":13.3,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144701141","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
Simultaneously Enhancing Energy Density and Reducing Cost of Vanadium Redox Flow Batteries Via the Dual Role of Tetravalent Vanadium Ions as Both Active Species and Redox Mediator. 通过四价钒离子作为活性物质和氧化还原介质的双重作用,同时提高钒氧化还原液流电池的能量密度和降低成本。
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-25 DOI: 10.1002/smll.202505171
Jia Liu,Yun Liu,Ziyi Dai,Fan Yang,Haoyao Rao,Lyuming Pan,Xiaoqian Xu,Meisheng Han,Lin Zeng,Yubai Li,Puiki Leung,Liang An,Lei Wei
{"title":"Simultaneously Enhancing Energy Density and Reducing Cost of Vanadium Redox Flow Batteries Via the Dual Role of Tetravalent Vanadium Ions as Both Active Species and Redox Mediator.","authors":"Jia Liu,Yun Liu,Ziyi Dai,Fan Yang,Haoyao Rao,Lyuming Pan,Xiaoqian Xu,Meisheng Han,Lin Zeng,Yubai Li,Puiki Leung,Liang An,Lei Wei","doi":"10.1002/smll.202505171","DOIUrl":"https://doi.org/10.1002/smll.202505171","url":null,"abstract":"Vanadium redox flow batteries (VRFBs) are promising for large-scale energy storage, but their commercialization is hindered by the high cost of vanadium electrolytes. This study introduces a cost-effective Mn-V/V redox flow battery by partially replacing vanadium ions with abundant manganese ions. Benefiting from the synergistic effect of VO2+, which functions both as an active species and a redox mediator, MnO2 precipitation resulting from the disproportionation of Mn3+ can be entirely dissolved during the discharge process. By optimizing the Mn/V ratio and using a polybenzimidazole (PBI) membrane, the system achieves an energy efficiency of 79.5% at 100 mA cm-2, exceeding conventional VRFBs by 1.6%. After 100 cycles, it retains 66.2% of discharge energy, significantly outperforming VRFBs (24.6%). When utilizing a Nafion 212 membrane, the Mn-V/Mn-V system delivers a coulombic efficiency of 98.7% at 300 mA cm-2 and 62.8% discharge energy retention after 100 cycles (200 mA cm-2), both surpassing that of VRFBs. Economic analysis further indicates that the Mn-V/V system can reduce electrolyte costs by up to 45% compared to VRFBs. This study expands the applicability of VRFBs technology and provides a viable pathway toward developing more affordable and sustainable long-duration energy storage systems.","PeriodicalId":228,"journal":{"name":"Small","volume":"704 1","pages":"e05171"},"PeriodicalIF":13.3,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144701400","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
Boron Vacancy Engineering in 2D WB-Based MBene Catalysts for Optimizing Lithium Polysulfide Reactions. 二维wb基MBene催化剂的硼空位工程优化锂多硫化反应。
IF 13.3 2区 材料科学
Small Pub Date : 2025-07-25 DOI: 10.1002/smll.202505919
Guifen Wu,Yunmiao Fan,Zihan Shen,Jiatong Li,Shuqi Yang,Zhenghua Wang,Huigang Zhang,Jun Pu
{"title":"Boron Vacancy Engineering in 2D WB-Based MBene Catalysts for Optimizing Lithium Polysulfide Reactions.","authors":"Guifen Wu,Yunmiao Fan,Zihan Shen,Jiatong Li,Shuqi Yang,Zhenghua Wang,Huigang Zhang,Jun Pu","doi":"10.1002/smll.202505919","DOIUrl":"https://doi.org/10.1002/smll.202505919","url":null,"abstract":"The shuttle effect of lithium polysulfides (LiPSs) and the slow conversion kinetics of sulfur have been hindering the commercial development of lithium-sulfur (Li-S) batteries. Herein, WB-VB based 2Dl MBene catalyst containing B vacancies is successfully prepared by a one-step room temperature F-free etching method. Both W and B atoms in this catalyst can interact with LiPSs simultaneously, effectively inhibiting the diffusion of soluble LiPSs. B-vacancy construction not only provides more exposure of active site W, but also improves the d band center, which is conducive to the rapid adsorption and Li-S reaction kinetics. More importantly, its mechanism for catalyzing LiPS reaction is characterized by in situ X-ray absorption spectroscopy. The results show that the reversible capacity is as high as 1485 mAh g-1 at 0.2 C, and 664 mAh g-1 even at 4 C. Furthermore, an outstanding capacity of 4.15 mAh cm-2 under high load of 4.36 mg cm-2 has remarkable cyclic stability.","PeriodicalId":228,"journal":{"name":"Small","volume":"122 1 1","pages":"e05919"},"PeriodicalIF":13.3,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144701038","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
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