过电位
塔菲尔方程
析氧
电解质
材料科学
电催化剂
无定形固体
化学工程
分解水
催化作用
电导率
无机化学
电极
化学
电化学
物理化学
有机化学
光催化
工程类
作者
Fei Hu,Shengli Zhu,Shuangming Chen,Yu Li,Lu Ma,Tianpin Wu,Yan Zhang,Chengming Wang,Congcong Liu,Xianjin Yang,Li Song,Xiaowei Yang,Yujie Xiong
标识
DOI:10.1002/adma.201606570
摘要
The intrinsic catalytic activity at 10 mA cm-2 for oxygen evolution reaction (OER) is currently working out at overpotentials higher than 320 mV. A highly efficient electrocatalyst should possess both active sites and high conductivity; however, the loading of powder catalysts on electrodes may often suffer from the large resistance between catalysts and current collectors. This work reports a class of bulk amorphous NiFeP materials with metallic bonds from the viewpoint of electrode design. The materials reported here perfectly combine high macroscopic conductivity with surface active sites, and can be directly used as the electrodes with active sites toward high OER activity in both alkaline and acidic electrolytes. Specifically, a low overpotential of 219 mV is achieved at the geometric current density 10 mA cm-2 in an alkaline electrolyte, with the Tafel slope of 32 mV dec-1 and intrinsic overpotential of 280 mV. Meanwhile, an overpotential of 540 mV at 10 mA cm-2 is attained in an acidic electrolyte and stable for over 30 h, which is the best OER performance in both alkaline and acidic media. This work provides a different angle for the design of high-performance OER electrocatalysts and facilitates the device applications of electrocatalysts.
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