化学
催化作用
氢氧化物
电催化剂
穆斯堡尔谱学
无机化学
镍
氧化物
共沉淀
氧化铁
热液循环
降水
析氧
化学工程
电极
电化学
物理化学
结晶学
气象学
有机化学
工程类
物理
生物化学
作者
Jamie Y. C. Chen,Lianna Dang,Hanfeng Liang,Wenli Bi,James B. Gerken,Song Jin,E. Ercan,Shannon S. Stahl
摘要
Nickel–iron oxides/hydroxides are among the most active electrocatalysts for the oxygen evolution reaction. In an effort to gain insight into the role of Fe in these catalysts, we have performed operando Mössbauer spectroscopic studies of a 3:1 Ni:Fe layered hydroxide and a hydrous Fe oxide electrocatalyst. The catalysts were prepared by a hydrothermal precipitation method that enabled catalyst growth directly on carbon paper electrodes. Fe4+ species were detected in the NiFe hydroxide catalyst during steady-state water oxidation, accounting for up to 21% of the total Fe. In contrast, no Fe4+ was detected in the Fe oxide catalyst. The observed Fe4+ species are not kinetically competent to serve as the active site in water oxidation; however, their presence has important implications for the role of Fe in NiFe oxide electrocatalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI