钴
热解
碳纤维
催化作用
材料科学
螯合作用
氮气
氧还原反应
氧还原
氧气
无机化学
化学工程
核化学
化学
电极
复合数
电化学
有机化学
物理化学
复合材料
工程类
作者
Yuan Gao,Xiaoman Gong,Haihong Zhong,Dianqing Li,Pinggui Tang,Nicolás Alonso‐Vante,Fengrui Sun
标识
DOI:10.1002/celc.202001090
摘要
Abstract A facile two‐step chemical route using cobalt ions coordinated with EDTA (Co II /EDTA chelate complex supported on glucose mixture), followed by the in situ pyrolysis process, from 500 to 900 °C, was developed to prepare Co embedded in N‐doped porous carbon hybrids (Co@C−T). The EDTA chelating agent served as both the N source and pore former. The physicochemical characterization results revealed that the pore structure, graphitization degree, and relative content of active centers, e. g., cobalt‐based components and nitrogen species, for Co@C−T electrocatalysts, were tailored by controlling the temperature of pyrolysis. The optimized material generated at 600 °C (Co@C‐600), showed an excellent oxygen reduction reaction activity with an onset potential of 0.91 V vs. RHE, and a half‐wave potential of 0.80 V vs. RHE. In addition, the Co@C‐600 catalyst showed superior durability and stability compared to the benchmark Pt/C.
科研通智能强力驱动
Strongly Powered by AbleSci AI