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用于碱金属离子电池的二维二氧化钛纳米片中与尺寸无关的快速离子插层

Size-Independent Fast Ion Intercalation in Two-Dimensional Titania Nanosheets for Alkali-Metal-Ion Batteries.

作者信息

Yang Jinlin, Xiao Xu, Gong Wenbin, Zhao Liang, Li Guohui, Jiang Kun, Ma Renzhi, Rummeli Mark H, Li Feng, Sasaki Takayoshi, Geng Fengxia

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, China.

A.J. Drexel Nanomaterials Institute and Department of Materials Science and Engineering, Drexel University, Philadelphia, PA, 19104, USA.

出版信息

Angew Chem Int Ed Engl. 2019 Jun 24;58(26):8740-8745. doi: 10.1002/anie.201902478. Epub 2019 May 16.

Abstract

Compared to lithium ions, the fast redox intercalation of large-radius sodium or potassium ions into a solid lattice in non-aqueous electrolytes is an elusive goal. Herein, by regulating the interlayer structure of stacked titania sheets through weakened layer-to-layer interactions and a robustly pillared gallery space, the two-dimensional channel between neighboring sheets was completely open to guest intercalation, allowing fast intercalation that was practically irrespective of the carrier-ion sizes. Regardless of employing regular Li or large-radius Na and K ions, the material manifested zero strain-like behavior with no significant change in both host structure and interlayer space, enabling comparable capacities for all tested ions along with excellent rate behaviors and extraordinarily long lifetimes, even with 80-μm-thick electrodes. The result highlights the importance of interlayer structural features for unlocking the electrochemical activity of a layered material.

摘要

与锂离子相比,大半径的钠离子或钾离子在非水电解质中快速氧化还原嵌入固体晶格是一个难以实现的目标。在此,通过减弱层间相互作用和构建坚固的柱撑层间空间来调控堆叠二氧化钛片层的层间结构,相邻片层之间的二维通道完全开放以允许客体嵌入,从而实现了几乎与载流子离子尺寸无关的快速嵌入。无论使用常规的锂离子还是大半径的钠离子和钾离子,该材料都表现出零应变样行为,主体结构和层间空间均无显著变化,使得所有测试离子都具有可比的容量,同时具有优异的倍率性能和超长的寿命,即使是80微米厚的电极也是如此。该结果突出了层间结构特征对于释放层状材料电化学活性的重要性。

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