材料科学
纳米颗粒
锂(药物)
电极
电解质
电化学
极化(电化学)
复合材料
复合数
铁电性
化学工程
纳米技术
电介质
光电子学
物理化学
医学
化学
工程类
内分泌学
作者
Miao Tian,Jing Lyu,Ran Su,Xu Zhang,Kexin Wang,Xiang Lv,Dawei Zhang,Shuo‐Wang Yang,John H. K. Yip,Zhongkai Hao,Guo Qin Xu
标识
DOI:10.1002/aenm.202401988
摘要
Abstract 2D Ti 3 C 2 T x MXene is a desirable electrode material for advanced lithium‐ion batteries (LIBs) in the pursuit of high energy and power densities, owing to its extensive reactive area and surface‐induced pseudo‐capacitance. Here, a novel synergistic strategy for fortifying lithium storage capability is first proposed, by in‐situ anchoring BaTiO 3 ferroelectric nanoparticles on few‐layered Ti 3 C 2 T x nanosheets (BT/f‐Ti 3 C 2 T x ) using a hydrothermal method. The uniform BaTiO 3 nanoparticles effectively prevent the restacking of Ti 3 C 2 T x nanosheets, successfully deplete metastable Ti atoms, and intriguingly form a thin and well‐adhered solid electrolyte interface layer, enhancing the aggregation‐resistant, oxidation‐resistant, and electrochemical properties of Ti 3 C 2 T x . Simultaneously, the internal electric fields, originating from the spontaneous polarization of BaTiO 3 ferroelectric nanoparticles, can augment the adsorption of Li + , boosting the lithium storage capacity and reaction kinetics. The resulting composite electrode displays a remarkable charge capacity of 84 mAh g −1 at 10 A g −1 , almost five times that of pristine Ti 3 C 2 T x electrode. The excellent rate performance and cyclability make BT/f‐Ti 3 C 2 T x composites highly attractive for LIBs. Furthermore, this synthetic approach presented here is scalable and can be extended to other Ti‐based materials. This strategy is expected to underscore the considerable potential of ferroelectric composites for integration into high‐performance LIBs.
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