Li‐rich rocksalt oxides are promising cathode materials for lithium‐ion batteries due to their large capacity and energy density, and their ability to use earth‐abundant elements. The excess Li in the rocksalt, needed to achieve good Li transport, reduces the theoretical transition metal redox capacity and introduces a labile oxygen state, both of which lead to increased oxygen oxidation and concomitant capacity loss with cycling. Herein, it is demonstrated that substituting the labile oxygen in Li‐rich cation‐disordered rocksalt materials with a vacancy is an effective strategy to inhibit oxygen oxidation. It is found that the oxygen vacancy in cation‐disordered lithium manganese oxide favors high Li coordination thereby reducing the concentration of unhybridized oxygen states, while increasing the theoretical Mn capacity. It is shown that in the vacancy‐containing compound, synthesized by ball milling, the Mn valence is lowered to less than +3, providing access to more than 300 mAh g−1capacity from the Mn2+/Mn4+redox reservoir. The increased transition metal redox and decreased O oxidation are found to improve the capacity and voltage retention, indicating that oxygen vacancy creation to remove the most vulnerable oxygen ions and reduce transition metal valence provides a new opportunity for the design of high‐performance Li‐rich rocksalt cathodes.
- Home
- Search Results
- Page 1 of 1
Search for: All records
-
Total Resources3
- Resource Type
-
00000030000
- More
- Availability
-
30
- Author / Contributor
- Filter by Author / Creator
-
-
Ceder, Gerbrand (3)
-
Tian, Yaosen (3)
-
Balasubramanian, Mahalingam (2)
-
Lun, Zhengyan (2)
-
Shi, Tan (2)
-
Aihara, Yuichi (1)
-
Clément, Raphaële J. (1)
-
Ha, Yang (1)
-
Huang, Jianping (1)
-
Kitchaev, Daniil A. (1)
-
Lee, Jinhyuk (1)
-
Lei, Teng (1)
-
McCloskey, Bryan D. (1)
-
Miara, Lincoln J. (1)
-
Ouyang, Bin (1)
-
Papp, Joseph K. (1)
-
Scott, M. C. (1)
-
Tsujimura, Tomoyuki (1)
-
Xiao, Yihan (1)
-
Yang, Wanli (1)
-
- Filter by Editor
-
-
& Spizer, S. M. (0)
-
& . Spizer, S. (0)
-
& Ahn, J. (0)
-
& Bateiha, S. (0)
-
& Bosch, N. (0)
-
& Brennan K. (0)
-
& Brennan, K. (0)
-
& Chen, B. (0)
-
& Chen, Bodong (0)
-
& Drown, S. (0)
-
& Ferretti, F. (0)
-
& Higgins, A. (0)
-
& J. Peters (0)
-
& Kali, Y. (0)
-
& Ruiz-Arias, P.M. (0)
-
& S. Spitzer (0)
-
& Sahin. I. (0)
-
& Spitzer, S. (0)
-
& Spitzer, S.M. (0)
-
(submitted - in Review for IEEE ICASSP-2024) (0)
-
-
Have feedback or suggestions for a way to improve these results?
!
Note: When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher.
Some full text articles may not yet be available without a charge during the embargo (administrative interval).
What is a DOI Number?
Some links on this page may take you to non-federal websites. Their policies may differ from this site.
-
-
Zhang, Ya‐Qian ; Tian, Yaosen ; Xiao, Yihan ; Miara, Lincoln J. ; Aihara, Yuichi ; Tsujimura, Tomoyuki ; Shi, Tan ; Scott, M. C. ; Ceder, Gerbrand ( , Advanced Energy Materials)
Abstract The interfacial instability between a thiophosphate solid electrolyte and oxide cathodes results in rapid capacity fade and has driven the need for cathode coatings. In this work, the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated LiNi0.5Co0.2Mn0.3O2cathodes are compared using first‐principles computations and electron microscopy characterization. Li3B11O18is identified as a superior coating that exhibits excellent oxidation/chemical stability, leading to substantially improved performance over cells with Li2ZrO3‐coated or uncoated cathodes. The chemical and structural origin of the different performance is interpreted using different microscopy techniques which enable the direct observation of the phase decomposition of the Li2ZrO3coating. It is observed that Li is already extracted from the Li2ZrO3in the first charge, leading to the formation of ZrO2nanocrystallites with loss of protection of the cathode. After 50 cycles separated (Co, Ni)‐sulfides and Mn‐sulfides can be observed within the Li2ZrO3‐coated material. This work illustrates the severity of the interfacial reactions between a thiophosphate electrolyte and oxide cathode and shows the importance of using coating materials that are absolutely stable at high voltage.
-
Lun, Zhengyan ; Ouyang, Bin ; Kitchaev, Daniil A. ; Clément, Raphaële J. ; Papp, Joseph K. ; Balasubramanian, Mahalingam ; Tian, Yaosen ; Lei, Teng ; Shi, Tan ; McCloskey, Bryan D. ; et al ( , Advanced Energy Materials)
Abstract The recent discovery of Li‐excess cation‐disordered rock salt cathodes has greatly enlarged the design space of Li‐ion cathode materials. Evidence of facile lattice fluorine substitution for oxygen has further provided an important strategy to enhance the cycling performance of this class of materials. Here, a group of Mn3+–Nb5+‐based cation‐disordered oxyfluorides, Li1.2Mn3+0.6+0.5
x Nb5+0.2−0.5x O2−x Fx (x = 0, 0.05, 0.1, 0.15, 0.2) is investigated and it is found that fluorination improves capacity retention in a very significant way. Combining spectroscopic methods and ab initio calculations, it is demonstrated that the increased transition‐metal redox (Mn3+/Mn4+) capacity that can be accommodated upon fluorination reduces reliance on oxygen redox and leads to less oxygen loss, as evidenced by differential electrochemical mass spectroscopy measurements. Furthermore, it is found that fluorine substitution also decreases the Mn3+‐induced Jahn–Teller distortion, leading to an orbital rearrangement that further increases the contribution of Mn‐redox capacity to the overall capacity.