双功能
过电位
催化作用
材料科学
碳纳米管
电池(电)
化学工程
析氧
双功能催化剂
合金
碳纤维
石墨烯
电极
无机化学
纳米技术
化学
电化学
复合数
物理化学
有机化学
冶金
复合材料
功率(物理)
工程类
物理
量子力学
作者
Xuan Xie,Hui Peng,Kanjun Sun,Xiaofei Lei,Ruiqi Zhu,Zhe Zhang,Guofu Ma,Ziqiang Lei
标识
DOI:10.1016/j.cej.2022.139253
摘要
Metal-based alloys encapsulated in nitrogen-doped carbon (alloy@NC) catalysts with high-efficiency and cost-effective are promising to solve the sluggish kinetics of the oxygen reduction/oxygen evolution reaction (ORR/OER) in Zn-air batteries (ZABs). Here, a novel FeNi3 alloy nanoparticles encapsulated by N-doped carbon graphene nanotubes (FeNi3@NC) catalyst with 0D/1D/3D multi-structure is synthesized through combining ligand-assisted and in-situ catalytic assembly strategy. The hybrid catalyst FeNi3@NC exhibited highly efficient ORR catalytic activity and stability. Impressively, the FeNi3@NC only required an overpotential of 291 mV to drive a current density of 10 mA cm−2, successfully demonstrating their excellent bifunctional catalytic activity. Moreover, the assembled rechargeable Zn-air battery based on FeNi3@NC air electrode exhibited high power density of 149.7 mW cm−2 and specific capacity of 658 mAh gZn-1, and long-term stability up to 280 h, outperforming most of the recently reported catalysts. Density functional theory (DFT) reveals that C atom adjacent to the pyridinic-N in FeNi3@NC act as the active sites for ORR/OER, since the alloying FeNi3 combined by pyridinic-N effectively break electroneutrality of the C atom, thereby accelerating the kinetics process of the ORR/OER. This work provides some constructive guidelines for fabricating alloy@NC catalysts with bifunctional catalytic activity and deeply demonstrates the applicability modulate the electronic configuration to construct high-performance rechargeable ZABs.
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