@article{Qin2024, 
author = {Jinlei Qin and Rui Wang and Zilong Yuan and Pei Xiao and Deli Wang},
title = {Manipulating fast Li2S redox via carbon confinement and oxygen defect engineering of In2O3 for lithium–sulfur batteries},
year = {2024},
journal = {Nano Research},
volume = {17},
number = {6},
pages = {5179-5187},
keywords = {oxygen vacancies, Li–S batteries, nitrogen-doped carbon confinement, bidirectional Li2S redox},
url = {https://www.sciopen.com/article/10.1007/s12274-024-6442-7},
doi = {10.1007/s12274-024-6442-7},
abstract = {Lithium–sulfur (Li–S) batteries have been considered as promising energy storage systems due to the merits of high energy density and low cost. However, the lithium polysulfides (LiPSs) diffusion and sluggish redox kinetics hamper the battery performance. In this work, low-bandgap indium oxide (In2O3) with dense oxygen vacancies (In2O3−x, 0 < x < 3) confined in nitrogen-doped carbon column (NC) is developed as a desirable LiPSs immobilizer and promoter to address these intractable problems. The NC confined In2O3−x with rich O vacancies (In2O3−x@NC) lowers the bandgap of 1.78 eV, strengthens the chemical adsorbability to LiPSs, and catalyzes the bidirectional Li2S redox. Attributed to the structural and chemical cooperativities, the obtained sulfur electrodes exhibit a stable cycling over 550 cycles at 1.0 C and splendid rate capability up to 4.0 C. More significantly, when the sulfur-loading reaches as high as 5.5 mg·cm−2, the cathodes achieve an areal capacity of 5.12 mAh·cm−2 at 0.1 C. The strategy of NC confined catalyst with rich defects engineering demonstrates great promise in the development of practical Li–S batteries.}
}