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用于可充电钠硫电池的单原子钇工程化双面电极

Single-Atom Yttrium Engineering Janus Electrode for Rechargeable Na-S Batteries.

作者信息

Zhang Erhuan, Hu Xiang, Meng Lingzhe, Qiu Min, Chen Junxiang, Liu Yangjie, Liu Guiyu, Zhuang Zechao, Zheng Xiaobo, Zheng Lirong, Wang Yu, Tang Wei, Lu Zhouguang, Zhang Jiatao, Wen Zhenhai, Wang Dingsheng, Li Yadong

机构信息

Department of Chemistry, Tsinghua University, Beijing 100084, China.

CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Provincial Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China.

出版信息

J Am Chem Soc. 2022 Oct 19;144(41):18995-19007. doi: 10.1021/jacs.2c07655. Epub 2022 Oct 10.

Abstract

The development of rechargeable Na-S batteries is very promising, thanks to their considerably high energy density, abundance of elements, and low costs and yet faces the issues of sluggish redox kinetics of S species and the polysulfide shuttle effect as well as Na dendrite growth. Following the theory-guided prediction, the rare-earth metal yttrium (Y)-N unit has been screened as a favorable Janus site for the chemical affinity of polysulfides and their electrocatalytic conversion, as well as reversible uniform Na deposition. To this end, we adopt a metal-organic framework (MOF) to prepare a single-atom hybrid with Y single atoms being incorporated into the nitrogen-doped rhombododecahedron carbon host (Y SAs/NC), which features favorable Janus properties of sodiophilicity and sulfiphilicity and thus presents highly desired electrochemical performance when used as a host of the sodium anode and the sulfur cathode of a Na-S full cell. Impressively, the Na-S full cell is capable of delivering a high capacity of 822 mAh g and shows superdurable cyclability (97.5% capacity retention over 1000 cycles at a high current density of 5 A g). The proof-of-concept three-dimensional (3D) printed batteries and the Na-S pouch cell validate the potential practical applications of such Na-S batteries, shedding light on the development of promising Na-S full cells for future application in energy storage or power batteries.

摘要

可充电钠硫电池的发展前景十分广阔,这得益于其相当高的能量密度、丰富的元素以及低成本,但同时也面临着硫物种氧化还原动力学缓慢、多硫化物穿梭效应以及钠枝晶生长等问题。根据理论指导预测,稀土金属钇(Y)-N单元已被筛选为一个有利的双面位点,用于多硫化物的化学亲和力及其电催化转化,以及可逆均匀的钠沉积。为此,我们采用金属有机框架(MOF)制备了一种单原子杂化物,其中钇单原子掺入氮掺杂的菱形十二面体碳主体(Y SAs/NC)中,该杂化物具有亲钠性和亲硫性的良好双面性质,因此在用作钠硫全电池的钠阳极和硫阴极主体时表现出非常理想的电化学性能。令人印象深刻的是,该钠硫全电池能够提供822 mAh g的高容量,并显示出超持久的循环稳定性(在5 A g的高电流密度下,1000次循环后容量保持率为97.5%)。概念验证的三维(3D)打印电池和钠硫软包电池验证了此类钠硫电池的潜在实际应用,为未来储能或动力电池中有望应用的钠硫全电池的发展提供了启示。

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