催化作用
介孔材料
碳纤维
化学
氧还原反应
甲醇
活性炭
氮气
杂原子
无机化学
材料科学
化学工程
有机化学
电化学
电极
吸附
复合材料
物理化学
工程类
复合数
戒指(化学)
作者
Yu Wang,Xu Jin,Ying Pan,Jianming Li,Ningning Guo
出处
期刊:ChemNanoMat
[Wiley]
日期:2018-07-11
卷期号:4 (9): 954-963
被引量:15
标识
DOI:10.1002/cnma.201800231
摘要
Abstract An activation step is essential for yielding nitrogen‐doped mesoporous carbon (NMCs) oxygen reduction reaction (ORR) electrocatalysts from biomass. Though many solely KOH or ZnCl 2 activated carbon materials have been synthesized with fine ORR activity, there a deep discussion of activated‐carbon‐based electrocatalysts obtained from different activation processes is still lacking. In this paper, we systemically compare radish‐derived NMCs that underwent different activation processes, and reveal the relationship between structure and activity of these activated carbons. We showed that though ZnCl 2 is not an effective porogen compared with KOH, owing to a more open pore structure along with effective preservation of nitrogen heteroatoms, ZnCl 2 assisted activated carbon could show significantly improved ORR activity, with an onset potential of 0.91 V (vs. RHE), close to benchmark Pt/C catalysts and even better extended operation stability and stronger tolerance to methanol crossover compared with commercial Pt/C catalysts. Thus we proved that ZnCl 2 assisted activation is better than exclusively self‐activation or KOH assisted activation in preparing biomass‐derived ORR catalysts.
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