Pd supported on Ti-suboxides as bifunctional catalyst for air electrodes of metal-air batteries

被引:29
作者
Alegre, C. [1 ]
Modica, E. [1 ]
Lo Vecchio, C. [1 ]
Siracusano, S. [1 ]
Arico, A. S. [1 ]
Baglio, V. [1 ]
机构
[1] CNR ITAE, Ist Tecnol Avanzate Energia, Salita Santa Lucia Contesse 5, I-98126 Messina, Italy
关键词
Pd catalysts; Titanium suboxides; Oxygen reduction reaction; Oxygen evolution reaction; Alkaline medium; Metal-air battery; REGENERATIVE FUEL-CELLS; OXYGEN REDUCTION REACTION; CARBON NANOFIBERS; ELECTROCATALYTIC ACTIVITY; DURABILITY; NANOPARTICLES; OXIDATION; DESIGN; PEMFC;
D O I
10.1016/j.ijhydene.2016.03.095
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Bifunctional air electrodes catalysing both the oxygen reduction and oxygen evolution reactions are essential in electrochemical devices such as metal-air batteries and regenerative fuel cells. Unfortunately, highly positive electrochemical potentials take place at the positive electrode (air electrode) especially during the oxygen evolution reaction. This is a highly corrosive condition and, thus, more stable catalysts are required. In the present work, titanium suboxides (TinO2-1) have been studied as palladium catalyst support for the air electrode of metal-air batteries. The performance of Pd/TinO2n-1 towards both the oxygen reduction and the oxygen evolution reactions in alkaline media was analysed. Besides, the stability of the catalysts was assessed by subjecting them to accelerated stress tests. These catalysts were compared to a Pd catalyst supported on a conventional carbon black (Vulcan). Pd/TinO2n-1 showed a suitable activity as bifunctional catalyst, comparable to Pd/Vulcan, particularly for the ORR. Besides, it showed a higher performance with time than the carbonaceous support-based catalyst when subjected to harsh electrochemical conditions (1.8 V vs. RHE for 8 h). This indicates a more suitable stability for application in metal-air batteries. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19579 / 19586
页数:8
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