析氧
生化工程
可再生能源
化学
理论(学习稳定性)
催化作用
燃料电池
氧气
电催化剂
阳极
合理设计
计算机科学
过电位
纳米技术
工艺工程
电化学
氧化还原
氧化物
塔菲尔方程
化学工程
无机化学
材料科学
电极
工程类
电气工程
物理化学
机器学习
作者
Aleksandar R. Žeradjanin,Justus Masa,Ioannis Spanos,Robert Schlögl
标识
DOI:10.3389/fenrg.2020.613092
摘要
Plotting the roadmap of future “renewable energy highway” requires drastic technological advancement of devices like electrolyzers and fuel cells. Technological breakthrough is practically impossible without advanced fundamental understanding of interfacial energy conversion processes, including electrocatalytic water splitting. Particularly challenging is the oxygen evolution reaction which imposes high demands on the long-term activity of electrocatalysts and electrode support materials. To cross the “Rubicon” and in a deterministic manner claim that we developed principles of rational catalyst design, we need first to comprehend the determinants of electrocatalytic activity as well as character of their time evolution. How reliable are reported activity and stability trends, could we interrelate activity and stability, and how meaningful that relation really is are some of the important questions that have to be tackled in building of a more comprehensive view on critically important anodic oxygen evolution.
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