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理解水分和二氧化碳参与的界面反应对金/二氧化锰催化的锂空气电池电化学性能的影响。

Understanding Moisture and Carbon Dioxide Involved Interfacial Reactions on Electrochemical Performance of Lithium-Air Batteries Catalyzed by Gold/Manganese-Dioxide.

作者信息

Wang Guoqing, Huang Liliang, Liu Shuangyu, Xie Jian, Zhang Shichao, Zhu Peiyi, Cao Gaoshao, Zhao Xinbing

机构信息

State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University , Hangzhou 310027, China.

Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province , Hangzhou 310027, China.

出版信息

ACS Appl Mater Interfaces. 2015 Nov 4;7(43):23876-84. doi: 10.1021/acsami.5b05250. Epub 2015 Oct 21.

DOI:10.1021/acsami.5b05250
PMID:26466174
Abstract

Lithium-air (Li-air) battery works essentially based on the interfacial reaction of 2Li + O2 ↔ Li2O2 on the catalyst/oxygen-gas/electrolyte triphase interface. Operation of Li-air batteries in ambient air still remains a great challenge despite the recent development, because some side reactions related to moisture (H2O) and carbon dioxide (CO2) will occur on the interface with the formation of some inert byproducts on the surface of the catalyst. In this work, we investigated the effect of H2O and CO2 on the electrochemical performance of Li-air batteries to evaluate the practical operation of the batteries in ambient air. The use of a highly efficient gold/δ-manganese-dioxide (Au/δ-MnO2) catalyst helps to understand the intrinsic mechanism of the effect. We found that H2O has a more detrimental influence than CO2 on the battery performance when operated in ambient air. The battery operated in simulated dry air can sustain a stable cycling up to 200 cycles at 400 mA g(-1) with a relatively low polarization, which is comparable with that operated in pure O2. This work provides a possible method to operate Li-air batteries in ambient air by using optimized catalytic electrodes with a protective layer, for example a hydrophobic membrane.

摘要

锂空气(Li-air)电池本质上是基于2Li + O2 ↔ Li2O2在催化剂/氧气/电解质三相界面上的界面反应来工作的。尽管近年来有所发展,但锂空气电池在环境空气中运行仍然是一个巨大的挑战,因为在界面上会发生一些与水分(H2O)和二氧化碳(CO2)相关的副反应,在催化剂表面形成一些惰性副产物。在这项工作中,我们研究了H2O和CO2对锂空气电池电化学性能的影响,以评估电池在环境空气中的实际运行情况。使用高效的金/δ-二氧化锰(Au/δ-MnO2)催化剂有助于理解这种影响的内在机制。我们发现,在环境空气中运行时,H2O对电池性能的不利影响比CO2更大。在模拟干燥空气中运行的电池在400 mA g(-1)下可稳定循环高达200次,极化相对较低,这与在纯O2中运行的情况相当。这项工作提供了一种通过使用带有保护层(例如疏水膜)的优化催化电极在环境空气中运行锂空气电池的可能方法。

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