Nitrate-mediated four-electron oxygen reduction on metal oxides for lithium-oxygen batteries

被引:12
|
作者
Zhu, Yun Guang [1 ]
Leverick, Graham [2 ]
Giordano, Livia [1 ,2 ,5 ]
Feng, Shuting [3 ]
Zhang, Yirui [2 ]
Yu, Yang [4 ]
Tatara, Ryoichi [1 ]
Lunger, Jaclyn R. [4 ]
Shao-Horn, Yang [1 ,2 ,4 ]
机构
[1] MIT, Res Lab Elect, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT, Dept Mech Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] MIT, Dept Chem Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] MIT, Dept Mat Sci & Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[5] Univ Milano Bicocca, Mat Sci Dept, R Cozzi 55, I-20126 Milan, MI, Italy
基金
加拿大自然科学与工程研究理事会;
关键词
RAMAN-SPECTRA; SODIUM; NIO;
D O I
10.1016/j.joule.2022.06.032
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
Li-O-2 batteries can provide greater gravimetric energy than Li-ion batteries but suffer from poor efficiency and cycle life due to the instability of aprotic electrolytes. In this study, we show that the apparent four-electron oxygen reduction to form Li2O in Li-O-2 ba-teries with molten nitrate is facilitated by the electrochemical reduction of nitrate to nitrite, and subsequent chemical oxidation of nitrite to nitrate by molecular oxygen, instead of a four-electron oxygen reduction aided by disproportionation of Li2O2 generated from two-electron reduction of molecular oxygen. By examining a series of transition metal catalysts using experiments and computation, optimizing the surface binding of nitrate to enhance the kinetics of the electrochemical reduction of nitrate to nitrite, as well as increasing the kinetics of nitrite oxidation by O-2 was shown to in-crease the discharge voltage and render the observed high-rate capability for NiO-based surfaces in Li-O-2 batteries.
引用
收藏
页码:1887 / 1903
页数:18
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