Monitoring the Local Coordination Evolutions in Li-Rich Cathode Materials via In Situ Raman Spectroscopy

被引:9
|
作者
Wang, Yanfang [1 ,2 ,3 ]
Li, Yingzhi [3 ]
Li, Zhiqiang [3 ]
Qin, Ning [3 ]
Wu, Feng [3 ]
Makepeace, Joshua W. [2 ]
Zhang, Fucai [1 ]
Allan, Phoebe K. [2 ]
Lu, Zhouguang [3 ]
机构
[1] Southern Univ Sci & Technol, Dept Elect & Elect Engn, Shenzhen 518055, Peoples R China
[2] Univ Birmingham, Sch Chem, Birmingham B15 2TT, England
[3] Southern Univ Sci & Technol, Dept Mat Sci & Engn, Shenzhen Key Lab Interfacial Sci & Engn Mat, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
REDOX CHEMISTRY; LI2RUO3; LITHIUM; TRANSFORMATION; TRANSITION; LI2MNO3; 3D;
D O I
10.1021/acsenergylett.3c02109
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Although consensus has been reached that the lattice oxygen (O2-) could be ultimately oxidized to molecular O-2 in lithium-rich cathode materials (LRCMs), monitoring the local coordination evolutions around oxygen in real time is still demanding. Herein, we demonstrate the potential of using in situ Raman spectroscopy to decipher the local environment changes upon de-/lithiation in Li2RuO3. Evolutions of both the Ru-Ru motions and Ru-O vibrations have been captured by in situ Raman tests and interpreted in combination with multimodal characterizations. Uniquely, triggering the anion redox reactions (ARRs) produces a Raman band (similar to 500 cm(-1)), which upon careful examination is attributed to the Ru-O-2(n-) (0 < n < 4) coordination and suggested as the indicator of O-O dimerization. Considering its nondestructivity and high sensitivity to lattice vibrations, this work could shed new light on utilizing Raman spectroscopy to investigate the local coordination evolutions in LRCMs and other materials.
引用
收藏
页码:4888 / 4894
页数:7
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