微型多孔材料
催化作用
纳米颗粒
氧还原反应
碳纤维
热解
介孔材料
化学工程
材料科学
多孔性
氧气
纳米技术
化学
物理化学
电极
电化学
有机化学
复合材料
工程类
复合数
作者
Xiangyu Lu,Yaqiang Li,Derui Dong,Yongbiao Wan,Ruopeng Li,Lihui Xiao,Dan Wang,Lilai Liu,Guangzhao Wang,Jinqiu Zhang,Maozhong An,Peixia Yang
标识
DOI:10.1016/j.jcis.2023.09.047
摘要
Fe single-atom catalysts still suffer from unsatisfactory intrinsic activity and durability for oxygen reduction reaction (ORR). Herein, the coexisting Fe single atoms and nanoparticles on hierarchically porous carbon (denoted as Fe-FeN-C) are prepared via a Zn5(OH)6(CO3)2-assisted pyrolysis strategy. Theoretical calculation reveals that the Fe nanoparticles can optimize the electronic structures and d-band center of Fe active center, hence reducing the reaction energy barrier for enhancing intrinsic activity. The Zn5(OH)6(CO3)2 self-sacrificial template not only can promote the formation of Fe single atoms, but also contributes to the construction of microporous/mesoporous/macroporous structures. Therefore, the obtained Fe-FeN-C exhibits impressive ORR activity with a half-wave potential of 0.921 V, which far exceeds Pt/C. With Fe-FeN-C as the cathode catalyst, the assembled Zn-air batteries delivered a maximum power density of 206 mW cm-2 and a long-cycle life over 400 h.
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