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5篇 您的检索式:作者名="Saana"
    题名 作者 年代 出处 被引量
1Single-Atom Catalysts for Electrochemical Hydrogen Evolution Reaction: Recent Advances and Future Perspectives显示文摘Hydrogen,a renewable and outstanding energy carrier with zero carbon dioxide emission,is regarded as the best alternative to fossil fuels.The most preferred route to large-scale production of hydrogen is by water electrolysis from the intermittent sources(e.g.,wind,solar,hydro,and tidal energy).However,the efficiency of water electrolysis is very much dependent on the activity of electrocatalysts.Thus,designing high-effective,stable,and cheap materials for hydrogen evolution reaction(HER)could have a substantial impact on renewable energy technologies.Recently,single-atom catalysts(SACs)have emerged as a new frontier in catalysis science,because SACs have maximum atom-utilization efficiency and excellent catalytic reaction activity.Various synthesis methods and analytical techniques have been adopted to prepare and characterize these SACs.In this review,we discuss recent progress on SACs synthesis,characterization methods,and their catalytic applications.Particularly,we highlight their unique electrochemical characteristics toward HER.Finally,the current key challenges in SACs for HER are pointed out and some potential directions are proposed as well.Zonghua Pu Ibrahim Saana Amiinu Ruilin Cheng Pengyan Wang Chengtian Zhang Shichun Mu Weiyue Zhao Fengmei Su Gaixia Zhang Shijun Liao Shuhui Sun 2020Nano-Micro Letters2020,12,2:10
2Invasive Group A Streptococcal Infections in Children: A Nationwide Survey in Finland显示文摘Terhi Tapiainen Saana Launonen Marjo Renko Harri Saxen Eeva Salo Matti Korppi Leena Kainulainen Tarja Heiskanen-Kosma Laura Lindholm Jaana Vuopio Tiina Huotari Jarmo Rusanen Matti Uhari 2016The Pediatric Infectious Disease Journal2016,,:1
3利用MOF-253衍生氮掺杂碳限域效应促进Pt纳米单晶电催化剂的氧析出反应显示文摘目前,为了有效解决电化学能量转化反应动力学过程缓慢和商业化应用等问题,需要大力提高催化剂的电催化活性和稳定性,并大幅降低贵金属催化剂的用量.通常,铂(Pt)基催化剂对燃料电池的氧还原反应(ORR)和水电解过程的氢析出反应(HER)表现出很高的活性.然而,对于高效的金属-空气电池和水电解装置,其中的氧析出反应(OER)则需要高活性的非Pt电催化剂来降低电化学过电位及提高其对高电位的耐受性.虽然相较于Pt催化剂,IrO2和RuO2等贵金属催化剂表现出了更高的OER活性,然而,它们的稳定性差,难以满足实际应用需求,严重阻碍了其在金属-空气电池和水电解中的应用.通常,Pt对OER的低效催化主要归因于在OER电催化过程中Pt与电解液直接接触,导致Pt表面快速被氧化,形成Pt氧化物(Pt^+4O2和Pt^+2O)层.形成的Pt氧化物对OER不起催化作用,从而降低了Pt的利用率和总的水电解效率.为了避免Pt表面的快速氧化,实现高的OER性能,我们将Pt金属纳米粒子有效地限域在超薄功能多孔碳层内.前期,已有大量的有关金属基ORR和HER催化剂研究证明,这种策略对于稳定金属纳米颗粒非常有效,可有效避免金属催化剂的快速氧化,而且还可抑制金属颗粒迁移和团聚;此外,还有利于增强催化剂的导电性和离子物种的扩散能力,从而提高催化剂的电催化性能.然而,要达到提高金属催化剂OER电催化性能的目的,还需要设计一种具有优良结构的功能化异质原子掺杂多孔碳基限域材料.金属有机框架(MOF),特别是MOF-253,由于具有较高的柔韧性、丰富的孔、可控的几何结构和高比表面积,被认为是制备功能多孔碳基限域材料的理想前驱体.为此,通过结合功能多孔碳基材料的限域作用及MOF-253和超细Pt纳米单晶的优势,本文合成了MOF-253衍生氮掺杂碳(N/C)限域的Pt纳米单晶(Pt@N/C)核壳型电催化剂.制备的Pt-N-C框架不仅具有超薄的氮掺杂活性多孔碳保护层壳体(平均厚度为0.51 nm),还有具高度分散和稳定化的Pt纳米单晶核体;值得指出的是,因受到碳层的限域作用,即使经900℃的高温处理,Pt纳米单晶仍保持了较小的晶体尺寸(平均粒径仅为6.7 nm);此外,该催化剂的Pt载量较低,仅为6.1wt%(Pt@N/C-10).将其作为OER电催化剂,表现出优异的OER性能:在10 mA cm^-2电流密度下,其过电位仅为298 mV,低于商业IrO2催化剂(353 mV);而且,经2000周加速电位扫描后,其电位仅降低19.4 mV,也低于IrO2(23.3 mV).本文很好地证明了通过构建空间限域结构可以有效解决Pt等金属催化剂因表面氧化而导致OER动力学活性和稳定性低的问题.Hellen Gabriela Rivera Monestel Ibrahim Saana Amiinu Andrés Alvarado González 蒲宗华 BibiMaryam Mousavi 木士春 2020Chinese Journal of Catalysis2020,41,5:1
4芬兰百分百显示文摘芬兰SAANA JA OLLI的包袋、桌布以及抱枕上的图案,都充满了北欧自然和人文风情,让人感觉到人与自然的亲近。不但设计的灵感来自芬兰的自然生活和人文传统,这些作品从设计,印花,到缝制,产品也全部在芬兰制作完成。msright Saana ja Olli Unto Rautio 2014设计2014,27,5:0
5A thin Si nanowire network anode for high volumetric capacity and long-life lithium-ion batteries显示文摘Silicon nanowires(Si NWs)have been widely researched as the best alternative to graphite anodes for the next-generation of high-performance lithium-ion batteries(LIBs)owing to their high capacity and low discharge potential.However,growing binder-free Si NW anodes with adequate mass loading and stable capacity is severely limited by the low surface area of planar current collectors(CCs),and is particularly challenging to achieve on standard pure-Cu substrates due to the ubiquitous formation of Li+inactive silicide phases.Here,the growth of densely-interwoven In-seeded Si NWs is facilitated by a thin-film of copper-silicide(CS)network in situ grown on a Cu-foil,allowing for a thin active NW layer(<10μm thick)and high areal loading(≈1.04 mg/cm^(2))binder-free electrode architecture.The electrode exhibits an average Coulombic efficiency(CE)of>99.6%and stable performance for>900 cycles with≈88.7%capacity retention.More significantly,it delivers a volumetric capacity of≈1086.1 m A h/cm^(3)at 5C.The full-cell versus lithium manganese oxide(LMO)cathode delivers a capacity of≈1177.1 m A h/g at 1C with a stable rate capability.This electrode architecture represents significant advances toward the development of binder-free Si NW electrodes for LIB application.Ibrahim Saana Amiinu Sumair Imtiaz Hugh Geaney Tadhg Kennedy Nilotpal Kapuria Shalini Singh Kevin M Ryan 2023Journal of Energy Chemistry2023,,6:0
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