电催化剂
材料科学
氧还原
氧还原反应
固态
Atom(片上系统)
氧气
对偶(语法数字)
还原(数学)
氧原子
纳米技术
工程物理
电极
物理化学
电化学
艺术
化学
几何学
文学类
数学
有机化学
分子
计算机科学
工程类
嵌入式系统
作者
Meng Du,Bingxian Chu,Qichen Wang,Cheng Li,Yu Lu,Zhan Zhang,Xin Xiao,Cong‐Qiao Xu,Meng Gu,Jun Li,Huan Pang,Qiang Xü
标识
DOI:10.1002/adma.202412978
摘要
Abstract Oxygen reduction reaction (ORR) electrocatalysts are essential for widespread application of quasi‐solid‐state Zn‐air batteries (ZABs), but the well‐known Fe‐N‐C single‐atom catalysts (SACs) suffer from low activity and stability because of unfavorable strong adsorption of oxygenated intermediates. Herein, the study synthesizes dual Fe/I single atoms anchored on N‐doped carbon nanorods (Fe/I‐N‐CR) via a metal–organic framework (MOF)‐mediated two‐step tandem‐pyrolysis method. Atomic‐level I doping modulates the electronic structure of Fe‐N x centers via the long‐range electron delocalization effect. Benefitting from the synergistic effect of dual Fe/I single‐atom sites and the structural merits of 1D nanorods, the Fe/I‐N‐CR catalyst shows excellent ORR activity and stability, superior to Pt/C and Fe or I SACs. When the Fe/I‐N‐CR is employed as cathode for quasi‐solid‐state ZABs, a high power density of 197.9 mW cm −2 and an ultralong cycling lifespan of 280 h at 20 mA cm −2 are both achieved, greatly exceeding those of commercial Pt/C+IrO 2 (119.1 mW cm −2 and 47 h). In addition, wide‐temperature adaptability and superior stability from −40 to 60 °C are realized for the Fe/I‐N‐CR‐based quasi‐solid‐state ZABs. This work provides a MOF‐mediated two‐step tandem‐pyrolysis strategy to engineer high‐performance dual SACs with metal/nonmetal centers for ORR and sustainable ZABs.
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