材料科学
瓦片
还原(数学)
Atom(片上系统)
固态
氧原子
化学工程
氧气
氧还原
纳米技术
冶金
工程物理
复合材料
物理化学
有机化学
分子
电极
电化学
嵌入式系统
化学
几何学
数学
计算机科学
工程类
作者
Bin Zhang,Jingshuang Dang,Hongyi Li,Jing Jing Wang,Donghao Xu,Shihua Jia,Mufei Li,Ling Huang,Jingui Duan
标识
DOI:10.1002/adfm.202502834
摘要
Abstract Oxygen reduction reaction plays a crucial role in energy‐related devices. However, four‐electron transfer process involved in this reaction is usually constrained by sluggish kinetics. Single atomic (SA) Fe catalysts have attracted extensive attention due to the high atom utilization, yet the impact of the support architecture on accelerating the reaction has been largely overlooked. Inspired by the edge‐rich and ordered tile that facilitates rainwater runoff, an orderly stacked “tile” carbon with highly dispersed SA Fe and doped S is prepared through the morphology‐persistent conversion of a new metal–organic framework with a “tile” assembly. The catalyst exhibits a higher half‐wave potential of 0.91 V in 0.1 M KOH, when compared with that of Pt/C and Fe atoms on a lamellar carbon. This is because the reaction kinetics is accelerated by the “tile” carbon architecture while the doped S weakens the Fe–O interaction, and decreases the *OH binding strength. Importantly, the catalyst, working at the air cathodes, powers the liquid and the solid‐state Zn–air batteries to show high‐power density and remarkable stability, and can effectively charge a mobile phone. This work not only provides an effective catalyst but also highlights the importance of “tile” architecture for developing advanced catalysts.
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