X射线光电子能谱
钛酸锂
扫描电子显微镜
结构精修
兴奋剂
阳极
材料科学
钛酸酯
分析化学(期刊)
锂(药物)
结晶学
化学
锂离子电池
晶体结构
物理化学
电极
陶瓷
光电子学
冶金
化学工程
电池(电)
复合材料
内分泌学
功率(物理)
工程类
物理
医学
量子力学
色谱法
作者
Basit Ali,Raz Muhammad,Iqra Moeez,Jae‐Ho Park,Mobinul Islam,Min-kyung Cho,Ji‐Young Kim,Kyung Yoon Chung,Kyung‐Wan Nam
标识
DOI:10.1002/adsu.202400337
摘要
Abstract A kinetically favored Cd 2+ and Ge 4+ dual‐doped lithium titanate (Li 4 Ti 5 O 12 ) anode material is designed for lithium‐ion batteries (LIBs). Rietveld refinement reveals that introducing a 0.05 wt.% of Cd 2+ at Li(8 a ) and Ge 4+ at Ti(16 d ) sites brings no structural change in the spinel Li 4 Ti 5 O 12 . Scanning transmission electron microscopy (STEM) identifies Cd 2+ and Ge 4+ are homogenously doped in the Li 4 Ti 5 O 12 lattice. High‐resolution powder diffraction (HRPD) confirmed that Cd 2+ and Ge 4+ doping in Li 4 Ti 5 O 12 brings expansion in the lattice, field emission scanning electron microscopy (FE‐SEM) shows the reduction in the particle size due to of Cd and Ge in the LTO lattice, and X‐ray photoluminescence spectroscopy (XPS) confirms the partial reduction of Ti 4+ to Ti 3+ ions on the surface of 0.05‐Cd‐Ge‐LTO electrodes to the pristine LTO. Furthermore, the 0.05‐Cd‐Ge‐Li 4 Ti 5 O 12 electrode exhibits a superior rate performance and delivers a discharge capacity of ≈169.1 mAhg −1 at 0.1 current rates. It is worth mentioning that, the 0.05‐Cd‐Ge‐Li 4 Ti 5 O 12 electrode brings outstanding cycling stability in Li + half‐cell, having a capacity retention of 98.79% after 300 cycles at 2C. This proves that dual‐doping of Cd 2+ at Li(8 a ) and Ge 4+ at Ti(16 d ) sites in the Li 4 Ti 5 O 12 lattice is an effective approach to obtain superior electrochemical performance as anode material in LIBs.
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