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TiNbC MXene cathode for high-performance aluminum-ion batteries 高性能铝离子电池用TiNbC MXene阴极
Communications Materials Pub Date : 2025-06-04 DOI: 10.1038/s43246-025-00829-9
Qicai Lin, Junjie Jin, Yongkang Jiang, Guan Sheng, Udo Schwingenschlögl, Junwei Wu, Shaobo Tu, Xingjun Liu, Xixiang Zhang
{"title":"TiNbC MXene cathode for high-performance aluminum-ion batteries","authors":"Qicai Lin, Junjie Jin, Yongkang Jiang, Guan Sheng, Udo Schwingenschlögl, Junwei Wu, Shaobo Tu, Xingjun Liu, Xixiang Zhang","doi":"10.1038/s43246-025-00829-9","DOIUrl":"https://doi.org/10.1038/s43246-025-00829-9","url":null,"abstract":"Al-ion batteries (AIBs) have emerged as a promising energy storage technology due to their high theoretical capacity, cost-effectiveness, and superior safety. However, the lack of stable and efficient cathode materials capable of reversible Al-complex ion (e.g., [AlCl4]−) insertion/extraction remains a critical challenge. In this work, we developed TiNbCTx MXene as a high-performance cathode material for AIBs, achieving remarkable capacity and cycling stability. Unlike symmetric-structured Ti2CTx, the TiNbCTx cathode leverages synergistic Ti–Nb bimetallic effects to enhance the electronic conductivity and electrochemical activity. Here we show, TiNbCTx delivers a high reversible capacity of 194 mAh·g−1 at 0.2 A·g−1 with 800-cycle stability. Through combined experimental characterization and density functional theory (DFT) calculations, we elucidate the kinetic mechanisms of energy storage, offering fundamental insights for the rational design of advanced cathode materials in AIBs. Aluminum-ion batteries require stable and efficient cathodes for reversible Al-complex ion insertion. Here, an TiNbCTx MXene is used as a cathode, achieving reversible capacity of 194 mAh·g−1 at 0.2 A·g−1, with 800-cycle stability.","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s43246-025-00829-9.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147898706","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Superconductivity of zirconium-nitrogen hydrides at megabar pressures 兆巴压力下锆氮氢化物的超导性
Communications Materials Pub Date : 2025-04-24 DOI: 10.1038/s43246-025-00808-0
Tao Luo, Shen-Ao Li, Liu-Cheng Chen, Guo-Hua Zhong, Hai-Qing Lin, Xiao-Jia Chen
{"title":"Superconductivity of zirconium-nitrogen hydrides at megabar pressures","authors":"Tao Luo, Shen-Ao Li, Liu-Cheng Chen, Guo-Hua Zhong, Hai-Qing Lin, Xiao-Jia Chen","doi":"10.1038/s43246-025-00808-0","DOIUrl":"https://doi.org/10.1038/s43246-025-00808-0","url":null,"abstract":"","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147334247","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cellulose composite membranes induced by multiple hydrogen bonds as lightweight current collectors for high-performance batteries 由多个氢键诱导的纤维素复合膜作为高性能电池的轻质集流器
Communications Materials Pub Date : 2025-04-22 DOI: 10.1038/s43246-025-00802-6
Chenchen Li, Zhenwei Yang, Xiaogang Luo
{"title":"Cellulose composite membranes induced by multiple hydrogen bonds as lightweight current collectors for high-performance batteries","authors":"Chenchen Li, Zhenwei Yang, Xiaogang Luo","doi":"10.1038/s43246-025-00802-6","DOIUrl":"https://doi.org/10.1038/s43246-025-00802-6","url":null,"abstract":"","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s43246-025-00802-6.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147334066","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Closed-loop enhancement of plant photosynthesis via biomass-derived carbon dots in biohybrids 生物杂交中生物质碳点对植物光合作用的闭环增强
Communications Materials Pub Date : 2025-03-02 DOI: 10.1038/s43246-025-00763-w
Wenbo Cheng, Xueyun Wang, Haitao Hu, Yang Yu, Xuemeng Yu, Weixiang Chao, Min Yu, Jianwei Ding, Yiliang Lin, Wei Zhao, Qiao Zhao, Rodrigo Ledesma‐Amaro, Chao Zhong, Lu Lü, Xihan Chen, Junzhong Liu, Chen Yang, Xiang Gao
{"title":"Closed-loop enhancement of plant photosynthesis via biomass-derived carbon dots in biohybrids","authors":"Wenbo Cheng, Xueyun Wang, Haitao Hu, Yang Yu, Xuemeng Yu, Weixiang Chao, Min Yu, Jianwei Ding, Yiliang Lin, Wei Zhao, Qiao Zhao, Rodrigo Ledesma‐Amaro, Chao Zhong, Lu Lü, Xihan Chen, Junzhong Liu, Chen Yang, Xiang Gao","doi":"10.1038/s43246-025-00763-w","DOIUrl":"https://doi.org/10.1038/s43246-025-00763-w","url":null,"abstract":"Improving photosynthetic efficiency is pivotal for biomanufacturing and agriculture. Despite the progress on photosynthetic biohybrids integrating biocatalysts with materials, nanomaterials with increasing energy-efficiency as well as great biocompatibility and cost-effectiveness are needed. Here, we present a closed-loop strategy using biomass-derived carbon dots (CDs) for improving photosynthesis. We demonstrate that the CDs act as both light converters and photosensitizers by converting solar irradiation to red light and supplying light-excited electrons into the photosynthetic electron transfer chain. Biohybrids incorporating CDs and cyanobacteria or plant exhibited increased photosynthetic efficiency, when compared with the photosynthetic organism only. The cyanobacterial CO2-fixation rate and CO2-to-glycerol production were increased 2.4-fold and 2.2-fold, respectively, while Arabidopsis thaliana displayed a 1.8-fold increase in the fresh weight of the plant. Techno-economic analysis showed the competitive advantage of biomass-derived CDs over other nanomaterials. These CDs hold potential applications in future sustainable agriculture and solar-powered biomanufacturing. Improving photosynthetic efficiency is crucial for CO>sub<2 > /sub < -based biomanufacturing and agriculture. Here, biomass-derived carbon dots in biohybrids are shown to enhance natural photosynthesis by converting solar irradiation to red light and supplying electrons to the photosynthetic electron transfer chain.","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s43246-025-00763-w.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147915980","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 28
Electrically chargeable inorganic persistent luminescence in an alternating current driven electroluminescent device 在交流电驱动的电致发光装置中可带电的无机持久发光
Communications Materials Pub Date : 2025-02-05 DOI: 10.1038/s43246-025-00746-x
Cunjian Lin, Rujun Yang, Zishuang Wu, Yajing Wang, Chenhan Zhan, H. Miyata, Xiankan Zeng, Yuantian Zheng, Shihai You, Ying Lv, Yixi Zhuang, Rong‐Jun Xie, Jumpei Ueda
{"title":"Electrically chargeable inorganic persistent luminescence in an alternating current driven electroluminescent device","authors":"Cunjian Lin, Rujun Yang, Zishuang Wu, Yajing Wang, Chenhan Zhan, H. Miyata, Xiankan Zeng, Yuantian Zheng, Shihai You, Ying Lv, Yixi Zhuang, Rong‐Jun Xie, Jumpei Ueda","doi":"10.1038/s43246-025-00746-x","DOIUrl":"https://doi.org/10.1038/s43246-025-00746-x","url":null,"abstract":"Persistent luminescence (PersL) in inorganic materials, lasting from seconds to even days, has attracted considerable attention. Despite the promise of electric power-driven PersL for lighting and display device applications due to its convenience and manageability, studies on electrically driven inorganic PersL are lacking. Here, we report an inorganic PersL in electroluminescent devices, which shows an energy storage effect that persists beyond 24 h after charging with an alternating current electric field at 250 K. The spin-coating method-prepared emission layer composites consist of a small bandgap copper-doped zinc sulfide core, a high dielectric constant alumina shell and a chemically passivated dielectric polydimethylsiloxane medium (ZnS:Cu@AlOx@PDMS), and these composites exhibit well-distributed electric fields and excellent operational stability. Thermoluminescence characterization reveal that PersL with an ~ 0.3 eV trap depth in electroluminescent devices mainly arises from the charge separation via hot-electron impact excitation and charge trapping within trap states in the emission layer. This study on electrically chargeable PersL in alternating current-driven electroluminescent devices can enhance our understanding of luminescence mechanisms in inorganic semiconductors. Persistent luminescence has potential in lighting and display applications but are studies are focused on photoexcitation rather than being electrically driven. Here, inorganic persistent luminescence is reported in an electroluminescent device with energy storage persisting over 24 h.","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s43246-025-00746-x.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147906764","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Reversibly thermosecreting and convertible lubricative oil-in-water mixtures using multiple hydrogen bonding interactions 利用多重氢键相互作用的可逆热分泌和可转换润滑油-水混合物
Communications Materials Pub Date : 2025-01-25 DOI: 10.1038/s43246-025-00740-3
Qianhui Zhou, Mingfei Li, Weiyan Yu, Yunjing Wang, Yujie Yang, Jingcheng Hao, Lu Xu
{"title":"Reversibly thermosecreting and convertible lubricative oil-in-water mixtures using multiple hydrogen bonding interactions","authors":"Qianhui Zhou, Mingfei Li, Weiyan Yu, Yunjing Wang, Yujie Yang, Jingcheng Hao, Lu Xu","doi":"10.1038/s43246-025-00740-3","DOIUrl":"https://doi.org/10.1038/s43246-025-00740-3","url":null,"abstract":"Achieving homogeneous oil and water mixing requires thorough droplet dispersions of both liquids. An additional component, such as a surfactant, particle, solvent or ion is normally required to stabilize the small liquid droplets by providing sufficiently low interfacial tensions or strong repulsive forces. Here we show that very stable oil-in-water mixtures can be created even at very high oil volume fractions by building multiple, high-strength hydrogen bonding interactions between water and a biocompatible and biodegradable oil trimethylolpropane trioleate, which make the oil molecules at the contact interface behave as pseudo-surfactants with ultrahigh interfacial activity. The resultant oil microdroplets can be reversibly thermosecreted from the continuous aqueous phase and lead to controllable formation/dissociation and switchable lubrication of the binary liquid mixture owing to the inherent thermal responsiveness of the intermolecular hydrogen bonding. Interestingly, although water is uncovered to possess a relatively poor lubricity, the liquid mixture yields an optimized lubrication that is even exceedingly comparable to pure oil at a water volume fraction as high as 80%. Oil-in-water mixtures can be controlled using components that interact with the oil/water interface. Here, an approach to produce stimuli-responsive and lubricative oil-in-water mixtures was demonstrated using multiple, high strength hydrogen bonds resulting in ultralow interfacial tension.","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s43246-025-00740-3.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147896925","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Continuous 1D single crystal growth with high aspect ratio by oriented aggregation of dendrite 通过枝晶定向聚集生长出具有高长径比的连续一维单晶
Communications Materials Pub Date : 2025-01-20 DOI: 10.1038/s43246-025-00737-y
Quan Wan, Maoqi Li, Yuhao Zhou, Meng Zhang, Zongpu Xu, Jie Wang, Yajun Shuai, Shuxu Yang, Mingying Yang
{"title":"Continuous 1D single crystal growth with high aspect ratio by oriented aggregation of dendrite","authors":"Quan Wan, Maoqi Li, Yuhao Zhou, Meng Zhang, Zongpu Xu, Jie Wang, Yajun Shuai, Shuxu Yang, Mingying Yang","doi":"10.1038/s43246-025-00737-y","DOIUrl":"https://doi.org/10.1038/s43246-025-00737-y","url":null,"abstract":"","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s43246-025-00737-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147330787","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction 强-弱双界面工程电催化剂用于大电流密度析氢反应
Communications Materials Pub Date : 2025-01-18 DOI: 10.1038/s43246-025-00735-0
Shaorou Ke, Ruiyu Mi, Xin Min, Xinyu Zhu, Congyi Wu, Xin Li, Bozhi Yang, Xiaowen Wu, Yangai Liu, Zhaohui Huang, Minghao Fang
{"title":"Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction","authors":"Shaorou Ke, Ruiyu Mi, Xin Min, Xinyu Zhu, Congyi Wu, Xin Li, Bozhi Yang, Xiaowen Wu, Yangai Liu, Zhaohui Huang, Minghao Fang","doi":"10.1038/s43246-025-00735-0","DOIUrl":"https://doi.org/10.1038/s43246-025-00735-0","url":null,"abstract":"Abstract Supported nanocatalysts are crucial for hydrogen production, yet their activity and stability are challenging to manage due to complex metal-support interfaces. Herein, we design Pt@ anatase&amp;rutile-TiO 2 with a strong-weak dual interface by modifying TiO 2 using high-energy ball milling and in-situ reduction to vary surface energies. Experiments and density functional theory calculations reveal that the strong Pt-anatase TiO 2 interface enhances hydrogen adsorption. In contrast, the weak Pt-rutile TiO 2 interface facilitates hydrogen desorption, simultaneously preventing Pt agglomeration and increasing reaction rate. As a result, the tailored catalyst has a 529.3 mV overpotential at 1000 mA cm −2 in 0.5 M H 2 SO 4 , 0.69 times less than commercial Pt/C. It also possesses 8.8 times the mass activity of commercial Pt/C and maintains a low overpotential after 2000 cyclic voltammetry cycles, suggesting high activity and stability. This strong-weak dual interface engineering strategy shows potential for overall water splitting and proton exchange membrane water electrolyzer, advancing the design of efficient supported nanocatalysts.","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s43246-025-00735-0.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147902223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Resolving the fundamentals of the J-integral concept by multi-method in situ nanoscale stress-strain mapping. 用多方法原位纳米应力-应变映射解决j积分概念的基本原理。
IF 7.5
Communications Materials Pub Date : 2025-01-01 Epub Date: 2025-02-22 DOI: 10.1038/s43246-025-00752-z
Michael Meindlhumer, Markus Alfreider, Noel Sheshi, Anton Hohenwarter, Juraj Todt, Martin Rosenthal, Manfred Burghammer, Enrico Salvati, Jozef Keckes, Daniel Kiener
{"title":"Resolving the fundamentals of the <i>J</i>-integral concept by multi-method in situ nanoscale stress-strain mapping.","authors":"Michael Meindlhumer, Markus Alfreider, Noel Sheshi, Anton Hohenwarter, Juraj Todt, Martin Rosenthal, Manfred Burghammer, Enrico Salvati, Jozef Keckes, Daniel Kiener","doi":"10.1038/s43246-025-00752-z","DOIUrl":"10.1038/s43246-025-00752-z","url":null,"abstract":"<p><p>The integrity of structural materials is oftentimes defined by their resistance against catastrophic failure through dissipative plastic processes at the crack tip, commonly quantified by the <i>J</i>-integral concept. However, to date the experimental stress and strain fields necessary to quantify the <i>J</i>-integral associated with local crack propagation in its original integral form were inaccessible. Here, we present a multi-method nanoscale strain- and stress-mapping surrounding a growing crack tip in two identical miniaturized fracture specimens made from a nanocrystalline FeCrMnNiCo high-entropy alloy. The respective samples were tested in situ in a scanning electron microscope and a synchrotron X-ray nanodiffraction setup, with detailed analyzes of loading states during elastic loading, crack tip blunting and general yielding, corroborated by a detailed elastic-plastic finite element model. This complementary in situ methodology uniquely enabled a detailed quantification of the <i>J</i>-integral along different integration paths from experimental nanoscale stress and strain fields. We find that conventional linear-elastic and elastic-plastic models, typically used to interpret fracture phenomena, have limited applicability at micron to nanoscale distances from propagating cracks. This for the first time unravels a limit to the path-independence of the <i>J</i>-integral, which has significant implications in the development and assessment of modern damage-tolerant materials and microstructures.</p>","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":"35"},"PeriodicalIF":7.5,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11846709/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143491098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of in situ tissue-engineered arteriovenous grafts suitable for cannulation in a large animal model. 在大型动物模型中评估适合插管的原位组织工程动静脉移植物。
IF 7.5
Communications Materials Pub Date : 2025-01-01 Epub Date: 2025-07-16 DOI: 10.1038/s43246-025-00879-z
Paul J Besseling, Wojciech Szymczyk, Martin Teraa, Raechel J Toorop, Paul A A Bartels, Boris Arts, Rob C H Driessen, Arturo M Lichauco, Hidde C Bakker, Joost O Fledderus, Gert J de Borst, Patricia Y W Dankers, Carlijn V C Bouten, Marianne C Verhaar
{"title":"Evaluation of in situ tissue-engineered arteriovenous grafts suitable for cannulation in a large animal model.","authors":"Paul J Besseling, Wojciech Szymczyk, Martin Teraa, Raechel J Toorop, Paul A A Bartels, Boris Arts, Rob C H Driessen, Arturo M Lichauco, Hidde C Bakker, Joost O Fledderus, Gert J de Borst, Patricia Y W Dankers, Carlijn V C Bouten, Marianne C Verhaar","doi":"10.1038/s43246-025-00879-z","DOIUrl":"10.1038/s43246-025-00879-z","url":null,"abstract":"<p><p>The sustainability of vascular access for hemodialysis is limited by frequent interventions and the inability of synthetic grafts to self-heal. Tissue engineering offers a solution through biodegradable grafts that remodel into autologous tissue. Here we assess electrospun polycarbonate-bis urea (PC-BU) vascular scaffolds (6mm-inner-Ø), reinforced with 3D-printed polycaprolactone coils, in a goat model, and compared them to expanded polytetrafluoroethylene (ePTFE) controls. The tissue-engineered grafts were repeatedly cannulated starting two weeks after implantation and were evaluated using computed tomography and histological analyses. By 12 weeks, the PC-BU grafts remodel into autologous tissue while maintaining structural integrity, maintaining integrity without dilations, ruptures, or aneurysms. Cannulation does not interfere with scaffold degradation or neo-tissue formation. Although the patency rate is lower for the PC-BU grafts (50%) compared to ePTFE (100%), the engineered grafts exhibit a self-healing response not seen in ePTFE. These findings demonstrate the potential of PC-BU tissue-engineered grafts as healing, functional vascular access solutions for hemodialysis, supporting cannulation during tissue transformation.</p>","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":"151"},"PeriodicalIF":7.5,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12267051/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144674036","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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