材料科学
阴极
兴奋剂
电化学
表面改性
氧化物
锂(药物)
扫描透射电子显微镜
密度泛函理论
透射电子显微镜
离子
扫描电子显微镜
过渡金属
表层
电子能量损失谱
分析化学(期刊)
化学工程
图层(电子)
纳米技术
复合材料
光电子学
物理化学
电极
冶金
计算化学
化学
工程类
生物化学
量子力学
色谱法
催化作用
医学
物理
内分泌学
作者
Zepeng Liu,Shuai Liu,Lu Yang,Chu Zhang,Xi Shen,Qinghua Zhang,Hong‐Ji Lin,Chine-Te Chen,Zhiwei Hu,Yuan Yang,Jun Ma,Richeng Yu,Xuefeng Wang,Zhaoxiang Wang,Liquan Chen
标识
DOI:10.1021/acsami.2c00155
摘要
Li-rich layer-structured oxides are considered promising cathode materials for their specific capacities above 250 mAh·g–1. However, the drawbacks such as poor rate performance, fast capacity fading, and the continuous transition metal (TM) migration into the Li layer hinder their commercial applications. To address these issues, surface doping of Ti and Zr was conducted to the Li- and Mn-rich layered oxide (LMR), Li1.2Mn0.54Ni0.13Co0.13O2. The drop of the average discharge potentials of the Ti- and Zr-doped LMR was reduced by 593 and 346 mV in 100 cycles, respectively. With aberration-corrected scanning transmission electron microscopy and electron energy loss spectroscopy, we clarified that Ti4+ and Zr4+ ions are located near the surface of the material, anchor the surface oxygen, and stabilize the LMR structure. The difference in the strengths of the Ti–O and Zr–O bonds and the doping-resultant electronic structures were determined with density functional theory (DFT) calculations and soft X-ray absorption spectroscopy (SXAS), responsible for the electrochemical performance of surface-doped materials. These findings verify our modification strategies to enhance the cycling performances of the promising LMR cathode materials.
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