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有序排列的偶极子调控源自阴离子的固体电解质界面以实现稳定的锂金属化学性质

Orderly Arranged Dipoles Regulate Anion-Derived Solid-Electrolyte Interphase for Stable Lithium Metal Chemistry.

作者信息

Xu Baolei, Ma Li, Wang Wenran, Zhu Hai, Zhang Youquan, Liang Chaoping, Zhou Liangjun, Wang Li, Zhang Yan, Chen Libao, Zhang Chunxiao, Wei Weifeng

机构信息

State Key Laboratory of Powder Metallurgy, Central South University, Changsha, Hunan, 410083, P. R. China.

Hunan Key Laboratory of Applied Environmental Photocatalysis, Changsha University, Changsha, Hunan, 410022, P. R. China.

出版信息

Adv Mater. 2024 May;36(18):e2311938. doi: 10.1002/adma.202311938. Epub 2024 Feb 5.

Abstract

Lithium (Li) metal batteries are considered the most promising high-energy-density electrochemical energy storage devices of the next generation. However, the unstable solid-electrolyte interphase (SEI) derived from electrolytes usually leads to high impedance, Li dendrites growth, and poor cyclability. Herein, the ferroelectric BaTiO with orderly arranged dipoles (BTOV) is integrated into the polypropylene separator as a functional layer. Detailed characterizations and theoretical calculations indicate that surface oxygen vacancies drive the phase transition of BaTiO materials and promote the ordered arrangement of dipoles. The strong dipole moments in BTOV can adsorb TFSI and NO anions selectively and promote their preferential reduction to form a SEI film enriched with inorganic LiF and LiNO species, thus facilitating the rapid transfer of Li and restraining the growth of Li dendrites. As a result, the Li-Li cell with the BTOV functional layer exhibits enhanced Li plating/stripping cycling with an ultra-long life of over 7000 h at 0.5 mA cm/1.0 mAh cm. The LiFePO || Li (50 µm) full cells display excellent cycling performance exceeding 1760 cycles and superior rate performance. This work provides a new perspective for regulating SEI chemistry by introducing ordered dipoles to control the distribution and reaction of anions.

摘要

锂(Li)金属电池被认为是下一代最具前景的高能量密度电化学储能装置。然而,由电解质衍生的不稳定固体电解质界面(SEI)通常会导致高阻抗、锂枝晶生长和较差的循环性能。在此,将具有有序排列偶极子的铁电体钛酸钡(BTOV)作为功能层集成到聚丙烯隔膜中。详细的表征和理论计算表明,表面氧空位驱动钛酸钡材料的相变并促进偶极子的有序排列。BTOV中强大的偶极矩可以选择性地吸附双三氟甲烷磺酰亚胺阴离子(TFSI)和硝酸根阴离子(NO ),并促进它们的优先还原以形成富含无机氟化锂(LiF)和硝酸锂(LiNO )物种的SEI膜,从而促进锂的快速传输并抑制锂枝晶的生长。结果,具有BTOV功能层的锂-锂电池在0.5 mA cm/1.0 mAh cm下表现出增强的锂电镀/剥离循环性能,超长寿命超过7000小时。磷酸铁锂||锂(50 µm)全电池显示出超过1760次循环的优异循环性能和卓越的倍率性能。这项工作通过引入有序偶极子来控制阴离子的分布和反应,为调节SEI化学提供了新的视角。

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