催化作用
部分
阴极
化学
燃料电池
氢
介孔材料
金属
密度泛函理论
无机化学
组合化学
材料科学
化学工程
有机化学
物理化学
计算化学
工程类
作者
Panpan Sun,Zelong Qiao,Shitao Wang,Danyang Li,Xuerui Liu,Qinghua Zhang,Lirong Zheng,Zhongbin Zhuang,Dapeng Cao
标识
DOI:10.1002/ange.202216041
摘要
Abstract To achieve practical application of fuel cell, it is vital to develop highly efficient and durable Pt‐free catalysts. Herein, we prepare atomically dispersed ZnNC catalysts with Zn‐Pyrrolic‐N 4 moieties and abundant mesoporous structure. The ZnNC‐based anion‐exchange membrane fuel cell (AEMFC) presents an ultrahigh peak power density of 1.63 and 0.83 W cm −2 in H 2 ‐O 2 and H 2 ‐air (CO 2 ‐free), and also exhibits long‐term stability with more than 120 and 100 h for H 2 ‐air (CO 2 ‐free) and H 2 ‐O 2 , respectively. Density functional calculations further unveil that the Zn‐Pyrrolic‐N 4 structure is the origin of high activity of as‐synthesized ZnNC catalyst, while the Zn‐Pyridinic‐N 4 moiety is inactive for oxygen reduction reaction (ORR), which successfully explain the puzzle why most Zn‐metal‐organic framework ‐derived ZnNC catalysts in previous reports did not present good ORR activity because of their Zn‐Pyridinic‐N 4 moieties. This work offers a new route for speeding up development of AEMFCs.
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