材料科学
电解质
电化学
锂(药物)
溶解
拉曼光谱
兴奋剂
阴极
透射电子显微镜
电极
离子
化学工程
高分辨率透射电子显微镜
纳米技术
光电子学
化学
光学
物理
工程类
内分泌学
物理化学
有机化学
医学
作者
Wei He,Pengfei Liu,Baihua Qu,Zhiming Zheng,Hongfei Zheng,Deng Pan,Pei Li,Shengyang Li,Hui Huang,Laisen Wang,Qingshui Xie,Dong‐Liang Peng
标识
DOI:10.1002/advs.201802114
摘要
Abstract The corrosion of Li‐ and Mn‐rich (LMR) electrode materials occurring at the solid–liquid interface will lead to extra electrolyte consumption and transition metal ions dissolution, causing rapid voltage decay, capacity fading, and detrimental structure transformation. Herein, a novel strategy is introduced to suppress this corrosion by designing an Na + ‐doped LMR (Li 1.2 Ni 0.13 Co 0.13 Mn 0.54 O 2 ) with abundant stacking faults, using sodium dodecyl sulfate as surfactant to ensure the uniform distribution of Na + in deep grain lattices—not just surface‐gathering or partially coated. The defective structure and deep distribution of Na + are verified by Raman spectrum and high‐resolution transmission electron microscopy of the as‐prepared electrodes before and after 200 cycles. As a result, the modified LMR material shows a high reversible discharge specific capacity of 221.5 mAh g −1 at 0.5C rate (1C = 200 mA g −1 ) after 200 cycles, and the capacity retention is as high as 93.1% which is better than that of pristine‐LMR (64.8%). This design of Na + is uniformly doped and the resultanting induced defective structure provides an effective strategy to enhance electrochemical performance which should be extended to prepare other advanced cathodes for high performance lithium‐ion batteries.
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