摘要
Oxygen evolution reaction has attracted extensive attention in energy conversion and storage technology (e.g. water splitting and rechargeable metal-air batteries). Its sluggish kinetics demands effective electrocatalysts to minimize the reaction barrier. Transition metal (oxy) hydroxides with a layered structure are one of the most active non-noble electrocatalysts. In this study, we compared the oxygen evolution performance of alpha-Co(OH)(2), beta-Co(OH)(2) and beta-CoOOH. Our results showed that alpha-type hydroxide is more active than beta-type with 60mV lower overpotential at 10mA/cm(2) and three times higher current density at 450mV overpotential. The plausible reason of this superior oxygen evolution activity is likely relevant to the large interlayer space in a-type hydroxide.
- 出版日期2016-6