析氧
材料科学
电解质
电极
催化作用
化学工程
贵金属
金属
电化学
氧气
分解水
冶金
化学
有机化学
物理化学
工程类
光催化
作者
Florian Moureaux,Philippe Stevens,Gwenaëlle Toussaint,Marian Chatenet
标识
DOI:10.1016/j.apcatb.2019.117963
摘要
316 L stainless steel (SS) electrodes were activated for the oxygen evolution reaction (OER) without addition of hetero-elements or incorporation of deposits at their surface. Such activation was either spontaneous (in situ: slow surface modification upon OER operation), or accelerated (ex situ, by alternating potential steps at low/high potential). Both techniques enable formation of a catalytic surface from the SS bulk components in experimental conditions close to those of usage, which guarantees long-term-stability and high-activity of the surfaces. Ex situ-activated electrodes show comparable performances than in situ-activated electrodes, the resulting OER activities in KOH electrolytes being high compared to other noble-metal-free electrocatalysts. Activated 316 L electrodes are remarkably stable in long-term OER operation (> 300 h). Therefore, cheap and widely-available activated-SS may be very competitive OER materials for alkaline water electrolyzers. These results open the way to the development of highly-active and low-cost OER materials for hydrogen production, or metal-air batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI