锰
材料科学
阴极
电化学
锂(药物)
氧化物
过渡金属
离子
锑
密度泛函理论
氧化锰
无机化学
化学
物理化学
电极
计算化学
催化作用
冶金
有机化学
内分泌学
医学
生物化学
作者
Fei Cao,Weihao Zeng,Jiawei Zhu,Jinsheng Xiao,Zilan Li,Ming Li,Rui Qin,Tingting Wang,Junxin Chen,Xiaoli Yi,Jiexi Wang,Shichun Mu
出处
期刊:Small
[Wiley]
日期:2022-05-12
卷期号:18 (24): e2200713-e2200713
被引量:29
标识
DOI:10.1002/smll.202200713
摘要
Abstract Owing to the interacted anion and cation redox dynamics in Li 2 MnO 3 , the high energy density can be obtained for lithium‐rich manganese‐based layered transition metal (TM) oxide [Li 1.2 Ni 0.2 Mn 0.6 O 2 , LNMO]. However, irreversible migration of Mn ions and oxygen release during highly de‐lithiation can destroy its layered structure, leading to voltage and capacity decline. Herein, non‐TM antimony (Sb) is pinned to the TM layer of LNMO by a facile sol‐gel method. High‐resolution ex and in situ characterization technologies manifest that the introduction of trace Sb inhibits the migration of Mn ions, forming a more stable structure. Sb can impressively adjust the Mn‐O interaction between anions and cations, beneficial to decrease the energy level of Mn 3d and O 2p orbitals and expand their band gap according to the theoretical calculation results. As a result, the discharge specific capacity and the energy density for SbLi 1.2 [Ni 0.2 Mn 0.6 ]O 2 (SLNMO) reaches as high as 301 mAh g −1 and 1019.6 Wh kg −1 at 0.1 C, respectively. Moreover, the voltage decay is reduced by 419.8 mV compared with LNMO. The regulative interaction between Mn 3d and isolated O 2p bands provides an accurate guidance for solving electrochemical performance deficiencies of lithium‐rich manganese‐based cathode oxide.
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