过电位
催化作用
电池(电)
材料科学
化学工程
氮气
金属
碳纤维
氮化物
比表面积
无机化学
复合数
化学
电化学
纳米技术
电极
冶金
复合材料
有机化学
物理化学
功率(物理)
物理
量子力学
图层(电子)
工程类
作者
Xiaoran Zhu,Jianze Zhang,Yan Wang,Mingsheng Yang,Haiping Yu,Tengfei Li,Mingjun Hu,Jun Yang
标识
DOI:10.1002/ente.202200602
摘要
It remains a challenge to achieve high‐performance, low‐cost, and robustly durable Fe, N co‐doped carbon‐based oxygen reduction reaction (ORR) catalysts with abundantly accessible Fe–N X sites. Herein, a novel scheme is designed to enrich the pore structure, increase the specific surface area, and generate spatially isolated Fe–N X sites of the ORR catalyst, in which pyridine nitrogen‐rich lamellar metal–organic complex (Fe–tetrapyridophenazine) is employed as the precursor and 2D graphitic carbon nitride (g‐C 3 N 4 ) as additional nitrogen source for achieving synergistic nitrogen‐doping effect. The introduction of g‐C 3 N 4 not only ameliorates the nitrogen coordination environment of metal active centers of the composite, but also increases the specific surface area and improves the pore structure. The resultant Fe–NC&CN composite has abundant active sites as well as remarkable electrical conductivity and suitable pore size for electron transfer and reactant diffusion. As expected, the catalyst exhibits excellent ORR activity, driving the reaction with low overpotential ( E 1/2 = 0.879 V) and remaining stable over a long reaction time (93% for 60 000 s), better than commercial Pt/C (20%) in all aspects. The assembled Zn–air battery exhibits high open‐circuit voltage of 1.566 V and high specific capacity of 815 mAh g Zn −1 , as well as stable and persistent discharge performance.
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