摘要
Currently,FeNi nanoalloys have received considerable attention for the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)in rechargeable aqueous zinc(Zn)-air batteries(ZABs)because of their high content and good chemical stability.However,their poor electronic conductivity,small surface area,and sluggish activity seriously hinder their catalytic performance.Herein,S-modulated FeNi nanoalloys supported by hierarchically porous carbon(SFeNi/PC)are synthesized through the thermal treatment of metal-organic precursors for efficient bifunctional oxygen catalysis.S decoration endows S-FeNi/PC with a superior OER performance while maintaining an ORR performance that is comparable to that of Pt/C.Hence,S-FeNi/PC exhibits excellent bifunctional oxygen catalytic activity,outperforming the noble-metal-based composite catalysts of Pt/C and RuO_(2).Notably,the ZABs assembled with S-FeNi/PC exhibit high specific capacity(792 mA h g^(-1)),high peak power density(123.5 mW cm^(-2)),and remarkable durability for 700 charge/discharge cycles at 10 mA cm^(-2),which surpasses the performance of commercially available Pt/C-RuOand other catalysts in previously reported studies.This study will provide not only new bifunctional oxygen electrodes for efficient ZAB devices but also new insights into the design of FeNi-based materials for a wide range of catalytic applications.
当前,FeNi合金由于其含量丰富、化学稳定性好的优点,在锌-空气二次电池(ZABs)中的氧还原反应(ORR)和析氧反应(OER)方面受到了广泛的关注.然而,传统FeNi合金还具有导电性差、比表面积小、活性低等缺点,严重阻碍了它们的催化性能.我们通过对金属有机前驱体进行热处理,合成了以分级多孔碳为载体的S-调控FeNi纳米合金材料(S-FeNi/PC),以实现高效的双功能氧催化.S调控赋予了FeNi纳米合金优越的OER性能,同时还使材料保持了与Pt/C相当的ORR性能.因此,SFeNi/PC具有很好的双功能氧催化活性,优于商业的Pt/C和RuO_(2)贵金属基复合催化剂.值得注意的是,以S-FeNi/PC为电极组装的ZABs具有较高的比容量(792 mA h g^(-1))、高峰值功率密度(123.5mW cm^(-2)),以及在10 mA cm^(-2)电流密度下可700次放电/充电循环的优异耐久性,这些性能远高于商用Pt/C-RuO_(2)催化剂,甚至超过了许多先前报道的工作.我们相信这项研究不仅为高效的ZABs装置提供了新的双功能氧电极材料,而且为具有广泛催化应用前景的FeNi基材料的设计提供了新的见解.
作者
Hailin Yu
Fei Fan
Chao He
Mi Zhou
Tian Ma
Yinghan Wang
Chong Cheng
余海林;范飞;何超;周密;马田;汪映寒;程冲(College of Polymer Science and Engineering,State Key Laboratory of Polymer Materials Engineering,Sichuan University,Chengdu 610065,China;Department of Ultrasound,West China Hospital,Sichuan University,Chengdu 610065,China;College of Biomass Science and Engineering,Sichuan University,Chengdu 610065,China)
基金
financially supported by the National Natural Science Foundation of China(22179087,51903178,and 51803134)
the Science and Technology Project of Sichuan Province(2021YFH0135)
China Postdoctoral Science Foundation(2021M692303)
the Post-doctor Research Project
and Sichuan University(2021SCU12013)。