质子交换膜燃料电池
催化作用
氧还原反应
化学工程
材料科学
电导率
电压
开路电压
耐久性
燃料电池
纳米技术
电极
化学
电化学
电气工程
复合材料
物理化学
有机化学
工程类
作者
Qiheng Wang,Jin Zhang,Xingdong Wang,Qingtao Liu,Jingjun Liu,Zhongbin Zhuang,Jianglan Shui
标识
DOI:10.1002/adsu.202300573
摘要
Abstract The practical application of non‐precious Fe─N─C catalysts in proton exchange membrane fuel cells (PEMFCs) continues to remain one of the major challenges due to their relatively poor oxygen reduction reaction (ORR) performance in acid. In this work, a fast and facilely performance enhancement strategy is first proposed for various Fe─N─C catalysts by supplying different direct‐current voltages to achieve a rapid solid‐state activation at room temperature. The voltage‐activated state‐of‐the‐art Fe─N─C catalyst has demonstrated a peak power density of 1.1 W cm −2 for PEMFC and remarkably increased long‐term durability for ORR. The substantially improved performance can be attributed to the formation of highly active ketone‐decorated (edge‐hosted) FeN 4 sites and substantially boosts coupled proton−electron transfer (CPET) by improving the conductivity of the as‐synthesized Fe─N─C with an interpenetrating network structure. The interconnected micro‐nodes within the interpenetrating network are the main active regions for the ORR, evidenced by an optimized structural model based on the above typical morphology. Therefore, this finding provides an innovative and facile idea for solving the activity and stability deficiency for promising Fe─N─C for commercial PEMFC.
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