阳极
材料科学
钾
化学工程
储能
透射电子显微镜
阴极
纳米技术
复合数
离子
电极
化学
复合材料
冶金
有机化学
量子力学
物理
工程类
物理化学
功率(物理)
作者
Yifan Xu,Hehe Zhang,Tangjing Ding,Ruiqi Tian,Dongmei Sun,Ming‐Sheng Wang,Xiaosi Zhou
标识
DOI:10.1007/s11426-022-1365-4
摘要
Due to their enormous potential for large-scale energy storage, rechargeable potassium-ion batteries have been widely researched and developed. However, the drastic volume change of electrode materials induced by the huge size of potassium ions during cycling remains a challenge for the construction of stable anodes. Herein, we propose a novel weak acid etching strategy to design and fabricate robust yolk-shell spheres with enough internal void space, in which the Bi2O3 nanospheres are well confined in the compartments of TiO2 submicrospheres (y-Bi2O3@TiO2). In situ transmission electron microscopy (TEM) and ex situ X-ray diffraction (XRD) are conducted to elucidate the structural evolution of y-Bi2O3@TiO2 and the interaction between K+ and Bi2O3 during cycling. Thanks to the yolk-shell nanoarchitecture and the superior buffering property of outer TiO2 covering, the as-obtained composite shows a high specific capacity of 383.5 mAh g−1 at 100 mA g−1, a considerable rate capacity of 134.1 mAh g−1 at 2 A g−1 and a stable cycling performance of 216.8 mAh g−1 at 500 mA g−1 over 500 cycles when used for potassium storage. Subsequently, the potassium-ion full battery, constructed by pairing y-Bi2O3@TiO2 anode with the thermally annealed 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) cathode, exhibits an outstanding cycling stability. Hopefully, this carefully-designed strategy can inspire the further development of superior energy storage materials in the near future.
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