首页> 外文期刊>Angewandte Chemie >Stabilizing the Oxygen Lattice and Reversible Oxygen Redox Chemistry through Structural Dimensionality in Lithium-Rich Cathode Oxides
【24h】

Stabilizing the Oxygen Lattice and Reversible Oxygen Redox Chemistry through Structural Dimensionality in Lithium-Rich Cathode Oxides

机译:通过富含锂的阴极氧化物中的结构维度稳定氧晶格和可逆氧氧化还原化学物质

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Lattice-oxygen redox (l-OR) has become an essential companion to the traditional transition-metal (TM) redox charge compensation to achieve high capacity in Li-rich cathode oxides. However, the understanding of l-OR chemistry remains elusive, and a critical question is the structural effect on the stability of l-OR reactions. Herein, the coupling between l-OR and structure dimensionality is studied. We reveal that the evolution of the oxygen-lattice structure upon l-OR in Li-rich TM oxides which have a three-dimensional (3D)-disordered cation framework is relatively stable, which is in direct contrast to the clearly distorted oxygen-lattice framework in Li-rich oxides which have a two-dimensional (2D)/3D-ordered cation structure. Our results highlight the role of structure dimensionality in stabilizing the oxygen lattice in reversible l-OR, which broadens the horizon for designing high-energy-density Li-rich cathode oxides with stable l-OR chemistry.
机译:格子氧氧化还原(L-或)已成为传统过渡金属(TM)氧化还原电荷补偿的必要伴侣,以在富含富锂的阴极氧化物中实现高容量。 然而,对L-或化学的理解仍然是难以捉摸的,并且一个关键问题是对L-或反应的稳定性的结构影响。 这里,研究了L-或结构维度之间的耦合。 我们揭示了具有三维(3D) - 分流阳离子框架的L-或富含量的TM氧化物上的氧气 - 晶格结构的演变是相对稳定的,这与明显扭曲的氧晶格直接对比 富含氧化物的框架,具有二维(2D)/ 3D订购阳离子结构。 我们的结果突出了结构维度在可逆L-OR中稳定氧气晶格的作用,或者扩大了用稳定的L-或化学设计高能密度锂的阴极氧化物的地平线。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号