Investigation of the Cathode-Catalyst-Electrolyte Interface in Aprotic Li-O2 Batteries

被引:48
|
作者
Schroeder, Marshall A. [1 ]
Pearse, Alexander J. [1 ]
Kozen, Alexander C. [1 ]
Chen, Xinyi [3 ]
Gregorczyk, Keith [1 ]
Han, Xiaogang [1 ]
Cao, Anyuan [4 ]
Hu, Liangbing [1 ]
Lee, Sang Bok [2 ]
Rubloff, Gary W. [1 ]
Noked, Malachi [2 ]
机构
[1] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[2] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[3] Lam Res Corp, Tualatin, OR 97062 USA
[4] Peking Univ, Dept Mat Sci & Engn, Beijing 100871, Peoples R China
关键词
LITHIUM-OXYGEN BATTERIES; LI-AIR BATTERIES; ATOMIC LAYER DEPOSITION; DIMETHYL-SULFOXIDE; CARBON; METAL; STABILITY; XPS; ELECTROCATALYSTS; SPECTROSCOPY;
D O I
10.1021/acs.chemmater.5b01605
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
Enabled by a unique integrated fabrication and characterization platform, X-ray photoelectron spectroscopy (XPS) studies reveal the formation of a thin solid electrolyte interphase (SET) layer on a Li-O-2 cathode after the first cycle. Subsequent cycling indicates that this SEI layer is very stable in terms of both chemistry and morphology, even after extensive cycling, preserving reversibility at the cathode/electrolyte interface. Remarkably, even after cell failure, replacement of the lithium anode resulted in recovery of the cycling behavior with the same cathode. These results demonstrate that chemical stabilization of the cathode/electrolyte interface promotes long-term operation of DMSO-based Li-O-2 Ru-catalyzed batteries. Characterization of the Li anode surface reveals electrolyte decomposition, and a partial mechanism is proposed for the observed chemical composition of the cathode SET. These studies are enabled by conformal deposition of a heterogeneous OER catalyst on a freestanding, binder-free, mesoporous, carbon-based Li-O-2 cathode with high capacity and long-term cycling stability.
引用
收藏
页码:5305 / 5313
页数:9
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