气凝胶
催化作用
碳纤维
材料科学
钴
化学工程
热解
碳纳米纤维
锌
纳米纤维
电池(电)
纳米技术
化学
碳纳米管
有机化学
复合材料
工程类
物理
复合数
功率(物理)
冶金
量子力学
作者
Mengxia Shen,Weihang Hu,Chao Duan,Ji Li,Shujiang Ding,Lilong Zhang,Jiahua Zhu,Yonghao Ni
标识
DOI:10.1016/j.jcis.2022.09.035
摘要
Single-atom catalysts (SACs) have opened up unprecedented possibilities for expediting oxygen reduction reaction (ORR) kinetics owing to their ultrahigh intrinsic activities. However, precisely controlling over the atomically dispersed metal-Nx sites on carbon support while fulfilling the utmost utilization of metal atoms remain the key obstacles. Here, atomically distributed Co-N4 sites anchored on N-doped carbon nanofibers aerogel (Co SAs/NCNA) is controllably attained through a direct pyrolysis of metal-chelated cellulose nanofibers (TOCNFs-Cd2+/Co2+) hydrogel precursor. The usage of Cd salt assists the assembly of cross-linked aerogel, creates a large number of interior micropores and defects, and favors the physical isolation of Co atoms. The hierarchically porous biomass carbon aerogel (2265.1 m2/g) offers an advantageous platform to facilitate accessibility of the catalytic centers, also renders rapid mass diffusion and electron-transfer paths throughout its 3D architecture. Notably, Co SAs/NCNA affords a paramount ORR activity and respectable durability when integrated into zinc-air battery devices.
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