Breaking the Activity-Stability Trade-off in Acidic OER via Mechanism Switching on Mo-Doped RuO(2)

通过 Mo 掺杂 RuO(2) 的机制转换打破酸性 OER 中的活性-稳定性权衡

阅读:1

Abstract

Ruthenium oxide (RuO(2)) is currently regarded as the preferred catalyst for the oxygen evolution reaction (OER) under acidic conditions. However, it faces issues of overoxidation and dissolution during the reaction process. Therefore, developing highly efficient and durable bifunctional electrocatalysts is crucial for acidic water electrolysis hydrogen production. This work reports a Ru-Mo bimetallic catalyst that enhances performance and stability in the acidic oxygen evolution reaction (OER) by incorporating Mo into RuO(2). The optimized Ru(1)Mo(1)-O/C exhibits an overpotential of only 167 mV at a current density of 10 mA·cm(-2), significantly lower than that of commercial RuO(2) (354 mV), with a Tafel slope of 57.7 mV·dec(-1), indicating fast kinetic rates. Furthermore, Ru(1)Mo(1)-O/C maintains durability for 255 h in 0.5 M H(2)SO(4) solution, offering a breakthrough in addressing the durability issue of ruthenium-based catalysts. Through the H/D isotope effect, we demonstrate that Mo incorporation accelerates proton reaction kinetics, providing strong evidence for suppressing Ru overoxidation.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。