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(De)Lithiation Mechanism of Li/SeS_x (x = 0-7) Batteries Determined by in Situ Synchrotron X-ray Diffraction and X-ray Absorption Spectroscopy

机译:原位同步加速器X射线衍射和X射线吸收光谱法测定Li / SeS_x(x = 0-7)电池的(去)锂化机理

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摘要

Electrical energy storage for transportation has gone beyond the limit of converntional lithium ion batteries currently. New material or new battery system development is an alternative approach to achieve the goal of new high-energy storage system with energy densities 5 times or more greater. A series of SeS_x-carbon (x = 0-7) composite materials has been prepared and evaluated as the positive electrodes in secondary lithium cells with ether-based electrolyte. In situ synchrotron high-energy X-ray difrraction was utilized to investigate the crystalline phase transition during cell cycling. Complementary, in situ Se K-edge X-ray absorption near edge structure analysis was used to track the evolution of the Se valence state for both crystalline and noncrystalline phases, including amorphous and electrolyte-dissolved phases in the (de)lithiation process. On the basis of these results, a mechanism for the (de)lithiation process is proposed, where Se is reduced to the polyselenides, Li_2Se_n (n ≥ 4), Li_2Se_2 and Li_2Se sequentially during the lithiation and Li_2Se is oxidized to Se through Li_2Se_n (n ≥ 4) during the delithiation. In addition, X-ray photoelectron spectroscopy and electrochemical impedance spectroscopy demonstrated the reversibility of the Li/Se system in ether-based electrolyte and the presence of side products in the carbonate-based electrolytes. For Li/SeS_2 and Li/SeS_7 cells, Li_2Se and Li_2S are the discharged products with the presence of Se only as the crystalline phase in the end of charge.
机译:目前,用于运输的电能存储已经超出了常规锂离子电池的极限。开发新材料或新电池系统是实现能量密度大于或等于5倍的新型高能量存储系统的目标的替代方法。制备了一系列SeS_x-碳(x = 0-7)复合材料,并将其评估为带有醚基电解质的二次锂电池中的正极。利用原位同步加速器高能X射线衍射研究细胞循环过程中的晶相转变。使用互补的原位Se K边缘X射线吸收近边缘结构分析来跟踪(去)锂化过程中晶相和非晶相(包括非晶相和电解质溶解相)的Se价态的演变。根据这些结果,提出了一种(去)锂化过程的机制,其中在锂化过程中将Se依次还原为多硒化物Li_2Se_n(n≥4),Li_2Se_2和Li_2Se,并且Li_2Se通过Li_2Se_n氧化为Se( n≥4)在脱锂过程中。另外,X射线光电子能谱和电化学阻抗谱证明了锂/硒体系在醚基电解质中的可逆性以及在碳酸盐基电解质中副产物的存在。对于Li / SeS_2和Li / SeS_7电池,Li_2Se和Li_2S是放电产物,只有Se作为充电末期的结晶相存在。

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  • 来源
    《Journal of the American Chemical Society》 |2013年第21期|8047-8056|共10页
  • 作者单位

    Chemical Science and Engineering Division Argonne National Laboratory, Argonne, Illinois 60439,United States;

    Chemical Science and Engineering Division Argonne National Laboratory, Argonne, Illinois 60439,United States;

    Chemical Science and Engineering Division Argonne National Laboratory, Argonne, Illinois 60439,United States;

    X-ray Science Division, Argonne National Laboratory, Argonne, Illinois 60439,United States;

    X-ray Science Division, Argonne National Laboratory, Argonne, Illinois 60439,United States;

    Chemical Science and Engineering Division Argonne National Laboratory, Argonne, Illinois 60439,United States;

    X-ray Science Division, Argonne National Laboratory, Argonne, Illinois 60439,United States;

    Chemical Science and Engineering Division Argonne National Laboratory, Argonne, Illinois 60439,United States;

    X-ray Science Division, Argonne National Laboratory, Argonne, Illinois 60439,United States;

    Chemical Science and Engineering Division Argonne National Laboratory, Argonne, Illinois 60439,United States,King Abdulaziz University, Jeddah, Saudi Arabia;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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