Lanthanum Manganite-based Air Electrode Catalysts and Their Application to Lithium-air Batteries: Effects of Carbon Support Oxidation
Lanthanum Manganite-based Air Electrode Catalysts and Their Application to Lithium-air Batteries: Effects of Carbon Support Oxidation
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DOI:
10.5796/electrochemistry.18-00034
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发表时间:
2018-09
期刊:
影响因子:
2.5
通讯作者:
Morihiro Saito;Y. Tachikawa;Taichi Fujinami;Kento Mikami;Yoshiya Hayashi;H. Shiroishi;D. Streich;Erik J. Berg;P. Novák
中科院分区:
文献类型:
--
作者:
Morihiro Saito;Y. Tachikawa;Taichi Fujinami;Kento Mikami;Yoshiya Hayashi;H. Shiroishi;D. Streich;Erik J. Berg;P. Novák
Acid-treated Ketjen Black (a-KB) carbon supports were prepared to investigate how oxidation of the carbon surface influences La0.6Sr0.4MnO3 (LSM) nanoparticle distribution, and conjugation to the carbon support. 30wt.% LSMloaded a-KB (LSM/a-KB) materials were prepared as air-electrode catalysts for rechargeable lithium-air batteries (LABs). a-KB exhibited a significant degree of O-containing (C-O, COO) surface functional groups, which resulted in the formation of smaller LSM nanoparticles and enhanced homogeneity over the carbon support when compared with the pristine KB support. Consequently, C-O-Mn bonds were formed, which increased the Mn oxidation state, and concomitantly enhanced conjugation resulting in improved catalytic activity. Additionally, the overpotential was reduced during charging (Li2O2 decomposition). Furthermore, LSM/a-KB enhanced the cyclability of the LAB test cell. Scanning electron microscopy observations revealed that LSM/a-KB efficiently decomposed the Li2O2 deposition layer, even after the 15th charge cycle when compared with LSM/KB. The LSM/a-KB air-electrode exhibited a more homogeneous and smaller-sized (and/or amorphous) Li2O2 deposition after discharging. Therefore, the oxidation of the carbon surface, resulting in enhanced LSM nanoparticle distribution on, and conjugation to, the a-KB surface, influences the homogeneity of the Li2O2 deposition onto the support during the discharge process leading to its facile decomposition during the following charge process. © The Electrochemical Society of Japan, All rights reserved.